Henrietta and David Lacks Henrietta Lacks' cells were essential in developing the polio vaccine and were used in scientific landmarks such as cloning, gene mapping and in vitro fertilization.

Courtesy of the Lacks family

Henrietta Lacks’ ‘Immortal’ Cells

Journalist Rebecca Skloot’s new book investigates how a poor black tobacco farmer had a groundbreaking impact on modern medicine

  • By Sarah Zielinski
  • Smithsonian.com, January 22, 2010

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    The Immortal Life of Henrietta Lacks

    by Rebecca Skloot
    Crown Publishing Group
    2010

    More from Smithsonian.com

    Medical researchers use laboratory-grown human cells to learn the intricacies of how cells work and test theories about the causes and treatment of diseases. The cell lines they need are “immortal”—they can grow indefinitely, be frozen for decades, divided into different batches and shared among scientists. In 1951, a scientist at Johns Hopkins Hospital in Baltimore, Maryland, created the first immortal human cell line with a tissue sample taken from a young black woman with cervical cancer. Those cells, called HeLa cells, quickly became invaluable to medical research—though their donor remained a mystery for decades. In her new book, The Immortal Life of Henrietta Lacks, journalist Rebecca Skloot tracks down the story of the source of the amazing HeLa cells, Henrietta Lacks, and documents the cell line's impact on both modern medicine and the Lacks family.

    Who was Henrietta Lacks?
    She was a black tobacco farmer from southern Virginia who got cervical cancer when she was 30. A doctor at Johns Hopkins took a piece of her tumor without telling her and sent it down the hall to scientists there who had been trying to grow tissues in culture for decades without success. No one knows why, but her cells never died.

    Why are her cells so important?
    Henrietta’s cells were the first immortal human cells ever grown in culture. They were essential to developing the polio vaccine. They went up in the first space missions to see what would happen to cells in zero gravity. Many scientific landmarks since then have used her cells, including cloning, gene mapping and in vitro fertilization.

    There has been a lot of confusion over the years about the source of HeLa cells. Why?
    When the cells were taken, they were given the code name HeLa, for the first two letters in Henrietta and Lacks. Today, anonymizing samples is a very important part of doing research on cells. But that wasn’t something doctors worried about much in the 1950s, so they weren’t terribly careful about her identity. When some members of the press got close to finding Henrietta’s family, the researcher who’d grown the cells made up a pseudonym—Helen Lane—to throw the media off track. Other pseudonyms, like Helen Larsen, eventually showed up, too. Her real name didn’t really leak out into the world until the 1970s.

    How did you first get interested in this story?
    I first learned about Henrietta in 1988. I was 16 and a student in a community college biology class. Everybody learns about these cells in basic biology, but what was unique about my situation was that my teacher actually knew Henrietta’s real name and that she was black. But that’s all he knew. The moment I heard about her, I became obsessed: Did she have any kids? What do they think about part of their mother being alive all these years after she died? Years later, when I started being interested in writing, one of the first stories I imagined myself writing was hers. But it wasn’t until I went to grad school that I thought about trying to track down her family.

    How did you win the trust of Henrietta’s family?
    Part of it was that I just wouldn’t go away and was determined to tell the story. It took almost a year even to convince Henrietta’s daughter, Deborah, to talk to me. I knew she was desperate to learn about her mother. So when I started doing my own research, I’d tell her everything I found. I went down to Clover, Virginia, where Henrietta was raised, and tracked down her cousins, then called Deborah and left these stories about Henrietta on her voice mail. Because part of what I was trying to convey to her was I wasn’t hiding anything, that we could learn about her mother together. After a year, finally she said, fine, let’s do this thing.

    When did her family find out about Henrietta’s cells?
    Twenty-five years after Henrietta died, a scientist discovered that many cell cultures thought to be from other tissue types, including breast and prostate cells, were in fact HeLa cells. It turned out that HeLa cells could float on dust particles in the air and travel on unwashed hands and contaminate other cultures. It became an enormous controversy. In the midst of that, one group of scientists tracked down Henrietta’s relatives to take some samples with hopes that they could use the family’s DNA to make a map of Henrietta’s genes so they could tell which cell cultures were HeLa and which weren’t, to begin straightening out the contamination problem.

    So a postdoc called Henrietta’s husband one day. But he had a third-grade education and didn’t even know what a cell was. The way he understood the phone call was: “We’ve got your wife. She’s alive in a laboratory. We’ve been doing research on her for the last 25 years. And now we have to test your kids to see if they have cancer.” Which wasn’t what the researcher said at all. The scientists didn’t know that the family didn’t understand. From that point on, though, the family got sucked into this world of research they didn’t understand, and the cells, in a sense, took over their lives.

    How did they do that?
    This was most true for Henrietta’s daughter. Deborah never knew her mother; she was an infant when Henrietta died. She had always wanted to know who her mother was but no one ever talked about Henrietta. So when Deborah found out that this part of her mother was still alive she became desperate to understand what that meant: Did it hurt her mother when scientists injected her cells with viruses and toxins? Had scientists cloned her mother? And could those cells help scientists tell her about her mother, like what her favorite color was and if she liked to dance.

    Deborah’s brothers, though, didn’t think much about the cells until they found out there was money involved. HeLa cells were the first human biological materials ever bought and sold, which helped launch a multi-billion-dollar industry. When Deborah’s brothers found out that people were selling vials of their mother’s cells, and that the family didn’t get any of the resulting money, they got very angry. Henrietta’s family has lived in poverty most of their lives, and many of them can’t afford health insurance. One of her sons was homeless and living on the streets of Baltimore. So the family launched a campaign to get some of what they felt they were owed financially. It consumed their lives in that way.

    What are the lessons from this book?
    For scientists, one of the lessons is that there are human beings behind every biological sample used in the laboratory. So much of science today revolves around using human biological tissue of some kind. For scientists, cells are often just like tubes or fruit flies—they’re just inanimate tools that are always there in the lab. The people behind those samples often have their own thoughts and feelings about what should happen to their tissues, but they’re usually left out of the equation.

    And for the rest of us?
    The story of HeLa cells and what happened with Henrietta has often been held up as an example of a racist white scientist doing something malicious to a black woman. But that’s not accurate. The real story is much more subtle and complicated. What is very true about science is that there are human beings behind it and sometimes even with the best of intentions things go wrong.

    One of the things I don’t want people to take from the story is the idea that tissue culture is bad. So much of medicine today depends on tissue culture. HIV tests, many basic drugs, all of our vaccines—we would have none of that if it wasn’t for scientists collecting cells from people and growing them. And the need for these cells is going to get greater, not less. Instead of saying we don’t want that to happen, we just need to look at how it can happen in a way that everyone is OK with.

    Medical researchers use laboratory-grown human cells to learn the intricacies of how cells work and test theories about the causes and treatment of diseases. The cell lines they need are “immortal”—they can grow indefinitely, be frozen for decades, divided into different batches and shared among scientists. In 1951, a scientist at Johns Hopkins Hospital in Baltimore, Maryland, created the first immortal human cell line with a tissue sample taken from a young black woman with cervical cancer. Those cells, called HeLa cells, quickly became invaluable to medical research—though their donor remained a mystery for decades. In her new book, The Immortal Life of Henrietta Lacks, journalist Rebecca Skloot tracks down the story of the source of the amazing HeLa cells, Henrietta Lacks, and documents the cell line's impact on both modern medicine and the Lacks family.

    Who was Henrietta Lacks?
    She was a black tobacco farmer from southern Virginia who got cervical cancer when she was 30. A doctor at Johns Hopkins took a piece of her tumor without telling her and sent it down the hall to scientists there who had been trying to grow tissues in culture for decades without success. No one knows why, but her cells never died.

    Why are her cells so important?
    Henrietta’s cells were the first immortal human cells ever grown in culture. They were essential to developing the polio vaccine. They went up in the first space missions to see what would happen to cells in zero gravity. Many scientific landmarks since then have used her cells, including cloning, gene mapping and in vitro fertilization.

    There has been a lot of confusion over the years about the source of HeLa cells. Why?
    When the cells were taken, they were given the code name HeLa, for the first two letters in Henrietta and Lacks. Today, anonymizing samples is a very important part of doing research on cells. But that wasn’t something doctors worried about much in the 1950s, so they weren’t terribly careful about her identity. When some members of the press got close to finding Henrietta’s family, the researcher who’d grown the cells made up a pseudonym—Helen Lane—to throw the media off track. Other pseudonyms, like Helen Larsen, eventually showed up, too. Her real name didn’t really leak out into the world until the 1970s.

    How did you first get interested in this story?
    I first learned about Henrietta in 1988. I was 16 and a student in a community college biology class. Everybody learns about these cells in basic biology, but what was unique about my situation was that my teacher actually knew Henrietta’s real name and that she was black. But that’s all he knew. The moment I heard about her, I became obsessed: Did she have any kids? What do they think about part of their mother being alive all these years after she died? Years later, when I started being interested in writing, one of the first stories I imagined myself writing was hers. But it wasn’t until I went to grad school that I thought about trying to track down her family.

    How did you win the trust of Henrietta’s family?
    Part of it was that I just wouldn’t go away and was determined to tell the story. It took almost a year even to convince Henrietta’s daughter, Deborah, to talk to me. I knew she was desperate to learn about her mother. So when I started doing my own research, I’d tell her everything I found. I went down to Clover, Virginia, where Henrietta was raised, and tracked down her cousins, then called Deborah and left these stories about Henrietta on her voice mail. Because part of what I was trying to convey to her was I wasn’t hiding anything, that we could learn about her mother together. After a year, finally she said, fine, let’s do this thing.

    When did her family find out about Henrietta’s cells?
    Twenty-five years after Henrietta died, a scientist discovered that many cell cultures thought to be from other tissue types, including breast and prostate cells, were in fact HeLa cells. It turned out that HeLa cells could float on dust particles in the air and travel on unwashed hands and contaminate other cultures. It became an enormous controversy. In the midst of that, one group of scientists tracked down Henrietta’s relatives to take some samples with hopes that they could use the family’s DNA to make a map of Henrietta’s genes so they could tell which cell cultures were HeLa and which weren’t, to begin straightening out the contamination problem.

    So a postdoc called Henrietta’s husband one day. But he had a third-grade education and didn’t even know what a cell was. The way he understood the phone call was: “We’ve got your wife. She’s alive in a laboratory. We’ve been doing research on her for the last 25 years. And now we have to test your kids to see if they have cancer.” Which wasn’t what the researcher said at all. The scientists didn’t know that the family didn’t understand. From that point on, though, the family got sucked into this world of research they didn’t understand, and the cells, in a sense, took over their lives.

    How did they do that?
    This was most true for Henrietta’s daughter. Deborah never knew her mother; she was an infant when Henrietta died. She had always wanted to know who her mother was but no one ever talked about Henrietta. So when Deborah found out that this part of her mother was still alive she became desperate to understand what that meant: Did it hurt her mother when scientists injected her cells with viruses and toxins? Had scientists cloned her mother? And could those cells help scientists tell her about her mother, like what her favorite color was and if she liked to dance.

    Deborah’s brothers, though, didn’t think much about the cells until they found out there was money involved. HeLa cells were the first human biological materials ever bought and sold, which helped launch a multi-billion-dollar industry. When Deborah’s brothers found out that people were selling vials of their mother’s cells, and that the family didn’t get any of the resulting money, they got very angry. Henrietta’s family has lived in poverty most of their lives, and many of them can’t afford health insurance. One of her sons was homeless and living on the streets of Baltimore. So the family launched a campaign to get some of what they felt they were owed financially. It consumed their lives in that way.

    What are the lessons from this book?
    For scientists, one of the lessons is that there are human beings behind every biological sample used in the laboratory. So much of science today revolves around using human biological tissue of some kind. For scientists, cells are often just like tubes or fruit flies—they’re just inanimate tools that are always there in the lab. The people behind those samples often have their own thoughts and feelings about what should happen to their tissues, but they’re usually left out of the equation.

    And for the rest of us?
    The story of HeLa cells and what happened with Henrietta has often been held up as an example of a racist white scientist doing something malicious to a black woman. But that’s not accurate. The real story is much more subtle and complicated. What is very true about science is that there are human beings behind it and sometimes even with the best of intentions things go wrong.

    One of the things I don’t want people to take from the story is the idea that tissue culture is bad. So much of medicine today depends on tissue culture. HIV tests, many basic drugs, all of our vaccines—we would have none of that if it wasn’t for scientists collecting cells from people and growing them. And the need for these cells is going to get greater, not less. Instead of saying we don’t want that to happen, we just need to look at how it can happen in a way that everyone is OK with.


     
    Comments

    Nice piece!

    Posted by Jeffro on January 28,2010 | 10:45 AM

    Excellent! Makes me want to buy the book!

    Posted by Cathy on January 28,2010 | 08:28 PM

    This is amazing! Just incredible!

    Posted by Jessica on February 1,2010 | 03:06 PM

    Can the family of H. Lacks file a lawsuit against the scientist?

    Posted by C. Frazier on February 1,2010 | 03:08 PM

    What are they planning on doing with those cells? They are not immortal they just outlived her. Everything that lives, dies, which means that they will die eventually.

    Posted by Colleen on February 1,2010 | 03:11 PM

    Fascinating article. I had just heard about the book earlier today, and I was hooked. Anyone know if the family ever was compensated?

    Posted by Susan on February 1,2010 | 03:13 PM

    sounds to me that the diseased cells are immortal ones and should be the story or the cause to cures.

    Posted by ch on February 1,2010 | 03:14 PM

    Fascinating story. Hopefully, it doesn't turn into a racial story. Black, white, yellow, etc. cells are needed to help people, whatever nationality, all over the world. Thank you HeLa, and God Bless!

    Posted by stacie on February 1,2010 | 03:16 PM

    Very interesting article. I feel these are stories our young people in school should hear about so they can understand the importance of science and research in their lives. Thank you.

    Posted by Jennifer on February 1,2010 | 03:16 PM

    great article. I am interested in reading the book. Too bad about the family not being compensated sooner.

    Posted by ceci on February 1,2010 | 03:17 PM

    Very interesting. I would love to read the book.

    Posted by Stephanie Kunz on February 1,2010 | 03:17 PM

    I like your article. Great analysis and comments.

    Posted by Panchoaventuras on February 1,2010 | 03:17 PM

    Awesome story;my curiosity is peaked also to the point of purchasing the book.

    Posted by Marie on February 1,2010 | 03:17 PM

    I was very interested in this story. I want to know more. Guess I'll have to buy the book.

    Posted by Blenda on February 1,2010 | 03:17 PM

    Awesome story;my curiosity is peaked also to the point of purchasing the book.

    Posted by Marie on February 1,2010 | 03:17 PM

    Fascinating facts! There should be a movie about this. She was a beautiful woman inside and out.

    Posted by Kelly Dunn on February 1,2010 | 03:18 PM

    Thank you for beautiful story. It is covered so many aspects of ours life. I think this article will inspire a lot of serious responds in near future. Marina

    Posted by marina on February 1,2010 | 03:18 PM

    SHE MUST BE A VAMPIRE

    Posted by COBY on February 1,2010 | 03:19 PM

    Wow! Talk about life after death! I will buy the book

    Posted by Shirley on February 1,2010 | 03:19 PM

    This is an incredible story!The part I find most worrying, is the fact that the writer did not disclose whether Henrietta's Family was compensated or not.This would have given the story a happy ending for most fair minded People.It is a very enlightening article regardless . Nice job

    Posted by Justin Dele Ajayi on February 1,2010 | 03:19 PM

    very interesting.

    Posted by JL on February 1,2010 | 03:19 PM

    Great story! Did the family receive restitution?

    Posted by Sherry on February 1,2010 | 03:20 PM

    Racist or not, taking someone's tissue without out their permission or knowledge and not informing the family is pretty sneaky and border line malicious.

    Posted by JT on February 1,2010 | 03:20 PM

    This would make an excellent documentary for a public broadcasting station

    Posted by t diamond on February 1,2010 | 03:20 PM

    I, too, am very interested in this! I had heard of HeLa cells, but never knew that they stood for a woman's name. I'm intersted in the poor woman who died so early in life and can't wait to read this book.

    Posted by amye on February 1,2010 | 03:21 PM

    hi, i am 15 years old and when i read this i was amazed, this is really cool and interesting

    Posted by hadley on February 1,2010 | 03:21 PM

    Somebody somewhere owes this family A LOT of money.

    Posted by deb carlsen on February 1,2010 | 03:21 PM

    This is such an interesting story. What great research this lady has done. I want to know more.

    Posted by Fay on February 1,2010 | 03:22 PM

    I WANT BUY THIS BOOK !! PRICE ? AND WHERE CAN GET IT .. PLS REPLY ANYONE.. TKS

    Posted by ap singh on February 1,2010 | 03:22 PM

    The world is a very very complicated place. Just the thought of this woman's cells floating through the air and infecting another set of cultured cells is amazing. And scary.

    Posted by Michael Herr on February 1,2010 | 03:22 PM

    Wow!!! Very interesting! I never knew there was such a a thing.

    Posted by Melissa on February 1,2010 | 03:22 PM

    this is a great story, fasinating. maybe she really was an angel on earth. over a 50 years,and all the lives hers has touched. i'm glad the story was told. i would love to read the book. her family should be proud.

    Posted by patty on February 1,2010 | 03:23 PM

    Did the family ever get any monies from this??????!!!!! They should have! I don't care if it was all for research and science!

    Posted by Donna on February 1,2010 | 03:23 PM

    If you know anything about history nothing about this women or man implies that they are poor. And, if they took her cells without her permission, I hope her family is still around to right whatever wrong was done to her!

    Posted by Sandra Hunt on February 1,2010 | 03:23 PM

    Sounds interesting, I love quirky biographies. I'll definitely be checking this one out.

    Posted by Nicky on February 1,2010 | 03:23 PM

    Very interesting article. It makes me want to learn more about the immortal cells and how the test are conducted. Knowledge is power!

    Posted by Nzinga on February 1,2010 | 03:23 PM

    I am totally facinated by this data. I never heard of HeLa cells. I don't have a medical background but I would love to read this book!

    Posted by Ann Osto on February 1,2010 | 03:24 PM

    OMG. Interesting, yet freakish

    Posted by Casey on February 1,2010 | 03:24 PM

    People don't realize it but we are all connected through DNA and the fact that Henrietta Lacks is a black woman who had cells that scientist were interested in doing research from, just shows that we all have something to contribute, Black or white. It is just interesting that this piece about cells and tissues are coming from a black Woman. Thank You

    Posted by Tracey Hainer on February 1,2010 | 03:24 PM

    As a human and a scientist I really appreciate this piece.

    Posted by Colleen on February 1,2010 | 03:24 PM

    "Floating on dust particles" Sounds like a serious contamination problem considering that her cells, when first taken, were cancerous.

    Posted by Edg1 on February 1,2010 | 03:24 PM

    Simply amazing/history unfolding before our eyes.

    Posted by Karl mclennon on February 1,2010 | 03:24 PM

    Wow. thats pretty interesting.

    Posted by Mar on February 1,2010 | 03:24 PM

    Well. Has the family received any money?

    Posted by wil on February 1,2010 | 03:24 PM

    I'll have to read this book. Sounds like it would be good and historically and scientifically informative.

    Posted by Naima Bullock on February 1,2010 | 03:24 PM

    Very nice; I, too, would now be interested in buying the book-

    Posted by Janet on February 1,2010 | 03:24 PM

    Very interesting article. I declined a personal call to finish the article ;)

    Posted by rz2853 on February 1,2010 | 03:24 PM

    Intresting! Makes you wander how many people this has happened too!

    Posted by Sharon Lemon on February 1,2010 | 03:25 PM

    Great article, stong and impressive content. Even i did not know this about cells.. This book should be on a PRESIDENTAL BOOK READING LIST, a must for Mankind.. Thanks for the time to get it out. Normally i by pass items.

    Posted by Carl Woodall on February 1,2010 | 03:25 PM

    I first read about immortal cells and this woman in Gerald B. Dermer's book "The Immortal Cell". Interesting stuff.

    Posted by Ken on February 1,2010 | 03:25 PM

    Very interesting. Reads like a good mystery book. Hooray for inquiring minds and persistence.

    Posted by Lahoma on February 1,2010 | 03:25 PM

    Was Henrietta's family ever compensated in any way for the sale / use of her cells?

    Posted by Christine Tiemann on February 1,2010 | 03:25 PM

    interesting did the family ever get paid, i want the book

    Posted by matt tomisin on February 1,2010 | 03:25 PM

    Was the family ever compensated for the selling of their mother's cells?

    Posted by stacey on February 1,2010 | 03:25 PM

    Very good article. I applaud your tenacity to discover the truth.

    Posted by Sebastian on February 1,2010 | 03:25 PM

    i will definitely buy the book. very intresting!

    Posted by will-e on February 1,2010 | 03:25 PM

    very interesting

    Posted by Roxane on February 1,2010 | 03:25 PM

    Very interesting! Indeed, it does make me want to buy the book!

    Posted by Christine Pacheco on February 1,2010 | 03:25 PM

    Great perseverance to uncover a wonderful story. Any explanation as to why these cells stayed alive?

    Posted by Charlynn on February 1,2010 | 03:26 PM

    Just astounding!!! The facts are amazing and the telling of it is very well done. I want the book also!!

    Posted by Holly on February 1,2010 | 03:26 PM

    Whow, amazing how one cell or culture can do all that. This makes me want to know more about the HeLa cells and her life.

    Posted by Wendy on February 1,2010 | 03:26 PM

    This is interesting. I plan to read the book. Very well written.

    Posted by Cindy on February 1,2010 | 03:26 PM

    WOW

    Posted by marcia on February 1,2010 | 03:26 PM

    I thought this piece was very interesting and informative. The family should be paid something and the truth should be written in the history books with other unwritten truths. Truth is always more interesting than fiction. I will seek out the book ,but I hope it goes further.

    Posted by Davee on February 1,2010 | 03:26 PM

    Very interesting

    Posted by Stacy on February 1,2010 | 03:26 PM

    Excellent Article!! Thank you for enlightening us, we now have yet another UNSUNG HERO to honor. I will be purchasing your book, keep writing.

    Posted by Mona on February 1,2010 | 03:26 PM

    Very interesting.Enjoyed reading it.

    Posted by maria zimmerman on February 1,2010 | 03:26 PM

    I learned about Henrietta in class! It's amazing to hear more about this woman and how she as contributed so much to medicine. This is something I'm sure she would be proud of. Amazing story!!!

    Posted by Carla on February 1,2010 | 03:26 PM

    Good piece of writing. I'm going to buy the book. Another piece of fact that African Americans contribute a lot to this great country and the world itself, even when they don't know it.

    Posted by Ron on February 1,2010 | 03:26 PM

    She was a very beatiful lady. Thank you Henrietta Lack for making history.

    Posted by Judy on February 1,2010 | 03:27 PM

    what happened to the family ?

    Posted by douglas on February 1,2010 | 03:27 PM

    I am amazed and awed by this story. I am sure if Henrietta had a voice today she would find immense peace in being immortal and significant in such a unique way. A woman in her social standing could never imagine in her wildest dreams that her name would be known globally. The human perspective of disease is a very tragic one however, the courage and endurance of the patient and the dedication of doctors make it an epic adventure where no matter what happens, heroes are there. Glad i took the time to read this!

    Posted by Dr. Amber Bokhari on February 1,2010 | 03:27 PM

    Very interesting. Awesome story! I truly desire to read this book.

    Posted by Shawn on February 1,2010 | 03:27 PM

    We are human at the time of conception.

    Posted by Dora L. Roazo on February 1,2010 | 03:27 PM

    did the family ever receive any monetary compensation?

    Posted by dee d on February 1,2010 | 03:27 PM

    All I can say is VAMPIRE!!!!

    Posted by Janiece Fisher on February 1,2010 | 03:27 PM

    Febuary 1, 2010 Very interesting, I will buy the book: Thanks

    Posted by Capitola on February 1,2010 | 03:27 PM

    Your article was very educational and uplifting. It makes you actually want to know more about this specimen we call a body.I would really like t own this book. Not so much scientifically but also spiritually!!!!

    Posted by Tel'Lisa on February 1,2010 | 03:27 PM

    That is a most amazing story!!

    Posted by Janet on February 1,2010 | 03:27 PM

    Is it not cool that Henrietta's cells have touched nearly everyone since 1951. Thanks Henrietta.

    Posted by Sid on February 1,2010 | 03:27 PM

    Henrietta virtually is living forever. We can thank her, her family and those who did the initial research which saved millions of lives. I think her family should be taken care of for life. Thank you.

    Posted by PENNY HAYES on February 1,2010 | 03:28 PM

    GREAT STORY

    Posted by Charlene Wilson on February 1,2010 | 03:28 PM

    No matter how it is sugar coated, it is about race. If Henritta had been a white woman this discovery would have been revealed years ago. The very thought that cells from a black woman could have this type of impact on the entire world is simply astounding,since some people consider Blacks less then human.

    Posted by marion brown on February 1,2010 | 03:28 PM

    What a wonderful piece of history, I will definitely purchase this book.

    Posted by Shirley on February 1,2010 | 03:28 PM

    Wow

    Posted by Alexis on February 1,2010 | 03:28 PM

    This is definitely a book I would like to possess. The research must have been invigorating and fulfilling in its completion.

    Posted by Lucretia Adams on February 1,2010 | 03:28 PM

    This article makes me want to read the book and more than that learn more about cell research.

    Posted by Norma on February 1,2010 | 03:28 PM

    I thought this article was very well written. Yes, it is true that what they did back in the 1950's was not ok especially looking back. Yet in that time, they did not really have the sophisticated science we have today. They did not realize the implication of what they were doing. Today I feel that you must sign a paper donating those cells to science. This would definitely stop further problems like with Henrietta Lacks family. I feel that considering how much Henrietta's cells have moved science forward and people have profited so much from them, then Henrietta's family should not have to live in poverty like they have. It should not have been kept such a secret (as it seemed to have been) to keep the family from making any kind of profit.

    Posted by Christine Poland on February 1,2010 | 03:28 PM

    Excellent story!

    Posted by Brenetta on February 1,2010 | 03:28 PM

    Very interesting story. I'd like to know more about Mrs. Henrietta Lack and ger family. Were her sons successful in their pursuit? What happened to her husband? Did Mrs. Lack die from cancer?

    Posted by Connie on February 1,2010 | 03:28 PM

    this is a very interesting story,wow.

    Posted by Jera on February 1,2010 | 03:29 PM

    Amazing and clear; I must have the book.

    Posted by Linda Davis on February 1,2010 | 03:29 PM

    did the family ever receive any money for the cells?

    Posted by anne berry on February 1,2010 | 03:29 PM

    That is one really amazing story. Henrietta's family should be very proud that their mother's cells saved millions of lives just through the polio vaccine alone. Thank you for such a wonderful story.

    Posted by Diana Watson on February 1,2010 | 03:29 PM

    Beautiful story

    Posted by Cheyenne on February 1,2010 | 03:29 PM

    I suppose it could be said that no matter how insignificant someone may suppose another person to be, there are many nameless people who have contributed significantly throughout the ages for the advancment of man; through their deeds, intellectual contributions etc. and in many cases, by reproduction. Here's one where genetic material was not passed on by the birth of a child but significant nevertheless, in its gift to mankind. I'm delighted that someone that would have been otherwise overlooked by historians now has been recognized for her contribution. Having been vacinated as a child against polio, I would like to thank Mrs. Lack for her cells.

    Posted by Charles Burnette on February 1,2010 | 03:29 PM

    Amazing. Will definitely put this on my to read list.

    Posted by Vanessa on February 1,2010 | 03:29 PM

    I will buy the book. I grew up in the 50's it was a wonderful time but so many things went on we still question.

    Posted by gertrudemanley on February 1,2010 | 03:29 PM

    WOW! If this person wrote her book as good as this piece was written, then its a book I would like to read. I get the feeling that she's not trying to sell her book, she's just trying to tell a story that needs to be told.

    Posted by Ann Phillips on February 1,2010 | 03:29 PM

    As a melanoma cancer survivor, whose tumor was removed at a cancer research facility in Buffalo NY in 1972, I chose immunotherapy follow up. Is there any way I might learn if my cells might have been harvested, utilized in cancer research, etc. Could they be in use today? I think that's really neat.

    Posted by mary on February 1,2010 | 03:29 PM

    Very Interesting Article.

    Posted by Valerie on February 1,2010 | 03:29 PM

    Rebecca Skloot is yet another in a long line of self-serving "experts" who have exploited Henrietta Lacks and her family. The "poor black" tobacco farmer, and her ignorant widower and children, being used as fodder for White Lady Skloot's artificial magnanimity is more than I can stomach right after lunch.

    Posted by William Thomas on February 1,2010 | 03:29 PM

    The story is incomplete as it relates to the family. What was the outcome of their lawsuit? Were they compensated? Thanks.

    Posted by Juanita Harris on February 1,2010 | 03:30 PM

    WOW, What a great way to start Black History month!!!!

    Posted by Corey Bivens on February 1,2010 | 03:30 PM

    outstanding

    Posted by Gederah on February 1,2010 | 03:30 PM

    Could donating cells for science be part of organ donation? Great story!!

    Posted by TT on February 1,2010 | 03:30 PM

    THAT WAS A NICE STORY!I ENJOYED IT !TO KNOW THAT THERE ARE CURES OUT HERE TO HELP THOSE IN NEED THANK YOU!

    Posted by JACQULINE COVINGTON on February 1,2010 | 03:30 PM

    I enjoyed the story but did the family ever receive any money from the sale of Henrietta's cells? Some people may think that the money is a minor story but for race of people who have not always received their fair share, it is important and should not be dismissed nor downplayed. The cells have helped all mankind over the years so let her cells help her family.

    Posted by Lester on February 1,2010 | 03:30 PM

    Wonderful report. SO much is owed this woman and her family. I think if she had known what good she has done she would not be mad.

    Posted by Bill on February 1,2010 | 03:30 PM

    Outstanding! Helps one to realize how far we have come and potential yet to be realized.

    Posted by Ty Ayers on February 1,2010 | 03:30 PM

    I studied about this lady five years ago. It's nice to see that the story is being shared among others. I am always interested in other cultures and their contribution to humanity. May this black history month be full of new knowledge to embrace unity and respect, instead of ethnocentrism and disunity among all cultures.

    Posted by limaya2003 on February 1,2010 | 03:30 PM

    I find this story to be so intrigueing. The history of Henrietta's cells can tell a beautiful story and help scientists to grow. I look forward to reading this book. I want to learn more about this subject and how this situation affected the family.

    Posted by Tamika Houston on February 1,2010 | 03:30 PM

    Wow, what a story.

    Posted by Deb Boyd on February 1,2010 | 03:30 PM

    I find this story to be so intrigueing. The history of Henrietta's cells can tell a beautiful story and help scientists to grow. I look forward to reading this book. I want to learn more about this subject and how this situation affected the family.

    Posted by Tamika Houston on February 1,2010 | 03:30 PM

    It did indeed make me want to read the book.I hope the family got some type of financial help from it. Also I hope her daughter and the family got to know more about themselves.It would seem they have helped a good many people.

    Posted by jim on February 1,2010 | 03:31 PM

    well how about that; here;s something other cultures can take home and have a conversation about over dinner hope they don;t choke ? in disbeleif; enjoy your meal.another great reason for black amer. like myself can feel proud once again we have made great strides and contributions to the world not only to america live on sister! live on!.

    Posted by mckinley on February 1,2010 | 03:31 PM

    If BILLIONS of $$$ were made off of HeLa cells why weren't Henrietta's family given a fair share of the profits?? Why WASN'T Henrietta told or ASKED for permission to use her cells??

    Posted by rjack58 on February 1,2010 | 03:31 PM

    very interesting story

    Posted by Ron on February 1,2010 | 03:31 PM

    Sensitively written,involving a very sensitive matter.

    Posted by Carolyn on February 1,2010 | 03:31 PM

    Wow-- the most interesting article I've read in years! Thanks for opening so many eyes to the unusual circumstances behind Ms. Lacks' invaluable contribution to health and science. Most of all, thank you, Henrietta.

    Posted by Lisa Nicole on February 1,2010 | 03:31 PM

    Looking forward to reading the book!

    Posted by Pendo on February 1,2010 | 03:31 PM

    OMG! Excellent work! Thank you not only for your expanded time in researching this "event," but paying attention to God's request of your talents! You have been blessed. I GREATLY look forward to owning this book and adding it to the hitory section of my personal library. Thank you!
    AK.

    Posted by Andrea K. Roth on February 1,2010 | 03:32 PM

    I was struck by the underlying assumption that scientists cling to: one size, or therapy, fits all. I am certainly not trained but I see that there is immeasurable variety in all things. Why then continue to assume that successful medicine for one patient or group will work on all patients? Genomics in its infancy points to tailored responses for specific conditions in widely varying settings. Patient X may be helped by therapy A while patient Y is not. We'll look back from years on and see how crude our assumptions were today just as we recoil from field conditions in the war between the states. The unique Henrietta cells were essential to many successes but that does not predict continued efficacy. We see how rapidly resistance develops, that should indicate some mortality of use. Fund genomic and stem cell research as if our future depends on its development. It does.

    Posted by Greg Hillman on February 1,2010 | 03:32 PM

    I had a problem with this statement "Deborah’s brothers, though, didn’t think much about the cells until they found out there was money involved" - (It's ok that some white guy makes billions on something stolen) They didn't come looking for the family until they needed to test on them again. postdoc called Henrietta’s husband one day. But he had a third-grade education and didn’t even know what a cell was. The way he understood the phone call was: “We’ve got your wife. She’s alive in a laboratory. We’ve been doing research on her for the last 25 years. And now we have to test your kids to see if they have cancer.” Which wasn’t what the researcher said at all. ( I understand his lack of trust, and how do you know what the postdoc actually said)

    Posted by Louise on February 1,2010 | 03:32 PM

    Great article to introduce Black History Month! Students in 6-12 should get this article, as I am tired of seeing students submit the most general personalities for essays during Black History Month. There are soooo many persons who have made an impact for African-Americans behind the scene and with products and patents that should have been filed for them, through history.

    Posted by Nadirah on February 1,2010 | 03:32 PM

    Hmm well considering you said "HIV tests, basic drugs and all of our vaccines" this leads me to believe that this is a good thing right... no, not at all. That's like saying, ok you can steal my cells and experiment on them all in the name of Science... hogwash. It is known that HIV was caused also basic drugs and vaccine's are all part of "Big Pharma". And the government has their little hands in it..

    Posted by Kristin on February 1,2010 | 03:32 PM

    Was Henrieta's family compensated after all? In any case, both scientists and Henrieta have saved so many through this research work. However, the donor should be proportionately honoured and or acknowledged.

    Posted by Audu Williams on February 1,2010 | 03:32 PM

    Very Interesting piece. I wonder how many other people are immortal through their cells.

    Posted by Valerie on February 1,2010 | 03:32 PM

    Very interesting!! I'll be looking for the book!!

    Posted by Samantha on February 1,2010 | 03:32 PM

    Its just another example of how back people have been involved in the furthering of science and the world. I think its very informative to know she was a black woman. Most people do think that all the great advances in the world come about by white American men, which is mostly never true.

    Posted by Delaine on February 1,2010 | 03:32 PM

    As a scientist, I have used HeLa cell in my research but never knew their origin. This is very interesting.

    Posted by Carl on February 1,2010 | 03:32 PM

    this makes me so intrested in cells. i want to learn more about the HeLa cell.

    Posted by Salcra on February 1,2010 | 03:32 PM

    Horrible piece! I understand this woman is now in it for the money made from book sales but dontcha think she could have told us exactly what is keeping these cells alive and why?

    Posted by rick h on February 1,2010 | 03:33 PM

    Fascinating!I agree with Cathy. :)

    Posted by Ally on February 1,2010 | 03:33 PM

    Actually this is nothing new! It is true and real, but unfortunately the "pharmacoindusty" a multi billion dollars industry my have all cure for all illness, but just because they are so greedy they do not develop the cures public. they just want to keep humans under medication and medication for ever for make billions and billions of dollars. I am sure of that.

    Posted by Jorge E. Adame on February 1,2010 | 03:33 PM

    Great story. However, I'm sure that the fact that this family was poor and black contributed to them not being compensated for this great contribution to medicine. It may have changed the course of this families future for generations. J

    Posted by JBM on February 1,2010 | 03:33 PM

    I love breakthrough stories like this because of her cells all humans has benefited including her family.

    Posted by Sandra on February 1,2010 | 03:34 PM

    This information is very interesting and it produces many questions relevant to various topics. I would like to read more!

    Posted by Ardin on February 1,2010 | 03:34 PM

    Very Interesting...Her family should be paid some money from the use of her cells. It is only the right thing to do since so many others are benefiting and making money off her cells that were taken unbeknownst to her.

    Posted by Mya on February 1,2010 | 03:34 PM

    This sounds like a very interesting story...I would love to read the book. It would also be great if they made a movie about this! :)

    Posted by kiarra on February 1,2010 | 03:34 PM

    Did ,or will,the family receive any of the money that resulted from this theft (that's essentially what happened)? I hope they do.

    Posted by Geoff on February 1,2010 | 03:35 PM

    WOW! Just goes to show you can learn something new everyday. This is an amazing story, hopefully Henrietta Lacks will get the credit she deserves. I would like to read the entire book.

    Posted by Jenny on February 1,2010 | 03:35 PM

    Creepy and cool at the same time. Mrs. Lacks has contributed so much to the health of the world's people. Definitely an interesting story. Blessings to her family. I'm hoping they're receiving financial benefit from the telling of the story and the research now. I'm a publisher and would be happy to work with the family to produce a book for struggling readers telling their family's story. They would benefit financially through a share of royalties.

    Posted by One Voice in Hawaii on February 1,2010 | 03:35 PM

    Very informative. I think I may get the book. Good Work!

    Posted by Asia on February 1,2010 | 03:35 PM

    WOW!!!!!!!!MAKES ME WANT TO READ MORE.EYES WERE AS BIG AS QUARTERS AS I READ.WOW!!!!!!!

    Posted by kittiecat on February 1,2010 | 03:35 PM

    Great story. African-Americans have contributed to all aspects of human advancement. Unfortunately, all Americans are not willing to admit to this fact.

    Posted by Darrin on February 1,2010 | 03:35 PM

    That was the most incredible story I have ever read. And the fact that it is true, is even more incredible. My question now is how many more people are walking around with immortal cells?

    Posted by Janie L.Johnson on February 1,2010 | 03:35 PM

    Excellent article.

    Posted by Jasmine on February 1,2010 | 03:36 PM

    Was the family compensated for the cells of their mother.

    Posted by Sheila on February 1,2010 | 03:36 PM

    brings 1950 science into the 21st century

    Posted by ellin on February 1,2010 | 03:36 PM

    I hope the family gets some money. What a cool story.

    Posted by Cesch on February 1,2010 | 03:36 PM

    This was a great story. I felt connected to it. I was born in 88, am a Biology teacher and live on Henrietta Street. Nice huh? I would love to share this book !

    Posted by Renda on February 1,2010 | 03:36 PM

    I find this very interesting and will want to buy the book. I would not have any issues with someone using my cells. I would even be willing to donate them. Therefore, I have a hard time understanding when people want to profit from them. Perhaps I do not understand the entire process.

    Posted by Debbie Cross on February 1,2010 | 03:36 PM

    Wonderful story , and so interesting. I look forward to reading more on this. It is a wonderful thing science is doing and I would hope to give my cells to be used, some day.I am white....

    Posted by June Droster on February 1,2010 | 03:36 PM

    What an amazing story.

    Posted by Dee on February 1,2010 | 03:37 PM

    Excellent article and insightful.

    Posted by John Moore on February 1,2010 | 03:37 PM

    I thought this was interesting. Sandra

    Posted by sandra black on February 1,2010 | 03:37 PM

    Such a great piece of history!I'm sure Henrietta's family would have never known what a great impact her life has effected this world.Just the world of medicine..

    Posted by Clarence on February 1,2010 | 03:37 PM

    Comments like Donna's show why many scientists (right or wrong) have avoided this question for so long. Tissue material removed in surgery or treatment is discarded material. Sometimes it can contribute to medical science - which benefits all of us - including Donna. It would be so honorable if most of us were altruistic and would generously do what we can to further medical research and treatment but so many people only see "what's in it for me". This is such a short-sighted, selfish, and ignorant perspective. That being said, I do believe in informed consent. This sounds like a book which should be read to the very end in order to grasp the author's support of cell research.

    Posted by Ron on February 1,2010 | 03:37 PM

    Interesting story. But why is always about money with some people?

    Posted by Tim on February 1,2010 | 03:37 PM

    Excellent. I really enjoyed this piece and have interest in this book! Cool!

    Posted by Latoriea on February 1,2010 | 03:38 PM

    very interesting subject, and way to look at it with a desire for peaceful resolution. How many of us have tissue somewhere being used for research and don't know about it? It raises many questions. I will read the book.

    Posted by Regine Verougstraete on February 1,2010 | 03:38 PM

    This is amazing! I am definitely buying the book. A great introduction to Black History Month.

    Posted by Nyesha Brooks on February 1,2010 | 03:38 PM

    This is an interesting story, and it makes me feel proud that an African American Woman's cell were able to save millions from having polio. The family should of never been told, the less some people are made aware of things they do not understand, the better off they are, the male portion of that family. One good thing, I got a chance to see a picture of a beautiful woman, now she is no longer a cell, she is a hero.

    Posted by Donna Childs on February 1,2010 | 03:38 PM

    Very interested in knowing more. Can't wait to buy the book.

    Posted by Ray on February 1,2010 | 03:38 PM

    Would these cells help cure some diseases?

    Posted by Christine Mattio on February 1,2010 | 03:38 PM

    Very intresting. I never really think about all that about cancer and cells, and usually when u do think about it, it's after u or the doctors discover u have it yourself. I mean i do think about it but it just didn't sink in till i read this article. So this article really makes u think or the book.

    Posted by Jillena on February 1,2010 | 03:39 PM

    This is like anything else. Had the lady been asked permission to have a tissue sample, she would probably have said, "Fine". If they had offered her $10 for the sample, she would likely have taken it. The fact that her cells were used to reach so many scientific benefits is fascinating, but one must wonder if someone else's cells would have accomplished the same purpose.

    Posted by M on February 1,2010 | 03:39 PM

    This is phenomenal. I just did some research online about where to get the book and Wikipedia had this info. The Immortal Life of Henrietta Lacks, Random House, ISBN 9-781-400-05217-2. Definitely something I would love to read.

    Posted by Heather on February 1,2010 | 03:39 PM

    This is really sad and interesting at the same time. I hope that the family gets some type of compensation, it sounds like they could really use it.

    Posted by jennerial on February 1,2010 | 03:39 PM

    Check Barnes & Noble.com: the book will be available tomorrow, Tuesday February 2, for approximately $16.00 online price.

    Posted by BJ on February 1,2010 | 03:39 PM

    Wow! First thought was to run out and buy the book so that I could read more. Second thought was to think that how much this should give back to the family, but make no mistake this is not about the money!

    Posted by Shereen August on February 1,2010 | 03:39 PM

    Very interesting story.

    Posted by Sabrina on February 1,2010 | 03:40 PM

    This is so amazing! I believe this to be very true when it comes to doctors and patients who are closer to their African Heritage (more melanin than others). I had a myelogram done years ago and I could see the doctor (periperally) handing his assistant a syringe of tissue taken from my spine. Never forgot this. Although Mrs. Lacks cells has helped a gazillion people look at the shadyness of the doctors then and even now. Why not inform the family? this is crazy! Write the book, please, please get the message out there. Africans in America are the most studied and the most copied. That's what happens when you are the 1st people.

    Posted by benita on February 1,2010 | 03:40 PM

    The Lt. Governor of South Carolina, Andre Bauer, needs to receive a copy of the book! I'll purchase two copies and send one to him.

    Posted by Darsha Doran on February 1,2010 | 03:40 PM

    Excellent article and facts! What about her parents and siblings were they included as part of the research? Would love to read and follow this story further. What can the family do to gain their fair share of what is being touted in your scientific report? Certainly they are entitled to some kind of monetary award. Jeannette

    Posted by Jeannette on February 1,2010 | 03:40 PM

    Unbelievable what can happen. I'll buy the book I'm facinated with this stuff

    Posted by Kathy on February 1,2010 | 03:40 PM

    why is she labeled as a "poor black tobacco farmer"? That label carries an inaccurate/misleading connotation. Should she not be more accurately identified as a "disenfranchised impoverished tobacco farmer"?

    Posted by smith on February 1,2010 | 03:40 PM

    Great story. This book is now next on my list of reading.

    Posted by Jennifer on February 1,2010 | 03:41 PM

    Thank you for sharing your experience and research about this topic! It was the first time I ever heard about this stuff, but I really agree with your perspective about understanding the best intentions of tissue culture! It was well written, I want to buy the book too!

    Posted by R. Ball on February 1,2010 | 03:41 PM

    Very Intresting!!! I had never heard of such a thing and am now curious as to why her cells, and only hers, are still alive to this day, guess i'm going to have to buy the book.

    Posted by Erica Riggs on February 1,2010 | 03:41 PM

    This is very interesting stuff! I have actually never heard of HeLa cells, but would like to learn more about it now! I would like to know why they are immortal cells? That's what is keeping me interested!

    Posted by Jessica on February 1,2010 | 03:41 PM

    This is a Wonderful story I have read. I have a real passion for the truth to come out. I would like for you to e-mail me this story to share with my family. THANk YOU Ms. DIANA L. Duff

    Posted by Diana Lynn Duff on February 1,2010 | 03:41 PM

    The reason she wasn't told and her family has never been given any compensation is because they didn't have to in the 1950's. None of what was done was illegal back then. People who say that her family should get money, where should they get it from? From people who have done nothing wrong?

    Posted by David on February 1,2010 | 03:42 PM

    Excellent! Bring fond memories of my 40 years in Laboratory Medicine

    Posted by larry on February 1,2010 | 03:42 PM

    Sounds a little SyFy

    Posted by Gene on February 1,2010 | 03:42 PM

    I FEEL PRIVILEGED AND THANKFUL TO HAVE READ THIS STORY. LIFE IS AN ENDLESS CHAIN OF NEGATIVE AND POSITIVE THAT GOES ON FOREVER AND WE ARE ALL LINKED IN OUR OWN EXPERIENCES. MAYBE THE GREAT PACIFIST LEADERS IN HISTORY WERE ABLE TO PERCEIVE OUR COMMONALITY AND TRIED TO TEACH US TO BE LOVING AND HELPFUL TO ALL LIVING THINGS.

    Posted by MIKE D on February 1,2010 | 03:42 PM

    Fascinating! Thank you Mrs. Lacks. You touched many lives.

    Posted by Honey B on February 1,2010 | 03:42 PM

    Very interesting story. I would also like to read the book.

    Posted by Sabrina on February 1,2010 | 03:42 PM

    http://topdocumentaryfilms.com/the-way-of-all-flesh/ Here is the Documentary... Really good watch

    Posted by Scott on February 1,2010 | 03:42 PM

    A very interesting read. I came across the Immortal HeLa cels of Henrietta Locks a few months ago. I'm glad it's being given even more recognition. Blacks have made great contribution to America and its ability to survive and thrive. Either with or without their knowledge and approval. From America's labor force to medicine, the military and beyond, blacks have made great contribution, only to be purposely written and hidden from mainstream American history. As America travels the globe demanding others of different beliefs, race, ethnicity etc. get along, it's long due for America to look at its own reflection in the mirror. As there remain areas and communities in America where a black man still can't freely drive or walk down the street without being stopped, beaten or even killed by police. Where a black soldier home on leave can be verbally and physically assaulted by police while simply walking on his own street after dark almost in front of the home he was born and raised, and his parents still live. There remain inequalities in the educational system and how black kids are dsciplined, suspended and even expelled from school. There are differences in everyday living for blacks. Simply going to the store to shop can have negative impacts on blacks. America before you send our sons and daughters off to fight and possibly die in war, all the while being led to believe they are dying so others can be free, remember there remains a significant level of injustices and practices that still talke place against minorities, especially black minorities, right here on your own soil and in a nation that holds itself up as the epitome and essence of what a FREE and DEMOCRATIC nation is suppose to be.

    Posted by Interesting And on February 1,2010 | 03:42 PM

    LOVE HOW THAT MAKE THE FAMILY OUT OUT BE GREEDY LOOSER THAT ONLY CARED ABOUT MONEY. BUT NOTHING ABOUT HOW THE DOCTORS WHERE MAKING MILLIONS OF DOLLARS OF THEIR MOTHERS CELLS AND NO ONE CALLS THEM GREEDY.!! THE STOLE THE WOMEN CELLS WITHOUT HER PERMISSION!!

    Posted by BOB ROC on February 1,2010 | 03:43 PM

    I have been looking at a way to help science after I am dead-At no cost to my family - Maybe something for them

    Posted by harriett e.robinson on February 1,2010 | 03:43 PM

    This is the most fascinating thing I have read in a long time!! I am definately going to look for the book! Thanks!

    Posted by Tammy on February 1,2010 | 03:43 PM

    I enjoyed reading this. I believe that there has been no wrong done to this patient or her family. When a patient [or family] signs for surgery any tisues harvested [or removed] can be used for testing or will be discarded. Usually this is explained and the patient is not compensated for this. And as far as the cells floating around, we are exposed to many infectious and cancer-causing particles--worry about them all.

    Posted by Linda on February 1,2010 | 03:43 PM

    I would like to know what percentage of the sales of this book, The Immortal Life of Henrietta Lacks, is going to go to Ms. Lacks heirs? I am glad that she brought to light. I wonder what happened to the scientist who took her cells with out Ms. Lacks permission? How rich did he get?

    Posted by Merriel on February 1,2010 | 03:43 PM

    this is a given for people like my self that has never had a knowledge of cells or a intrest of them. i can say i want to know now all i can about cells now. and need to know how i can get the book. thanks for the eye opener! BILLY

    Posted by billy williams on February 1,2010 | 03:43 PM

    Great!!! I learned something!Thanks for her Cell ,because of that we discover something new,and I hope it will be use for better.

    Posted by anne on February 1,2010 | 03:43 PM

    Money,money,money. Only in America could this story result in the greedy response----MONEY.

    Posted by S.Laughridge on February 1,2010 | 03:43 PM

    It won't be long when the media get a hold of this, then the ACLU, then so on and on...., with so much benefits this provides, how is it that the source was forgotten? I am for advancement in new cures and am sure the founders were hansomely rewarded. It seems as though a foundation needs to be made on behalf of the Henrietta Lacks and its family and its proceeds excess from donors and residual income from the Hella Cells for as long as it lives or utilize should be use to provide 100% scholarship for any education of their choosing if so they please. A quarterly proceeds should be disburse among the original sibling then devi up the next generation downline. This is my two cents from outside looking in and taking this article at face value.

    Posted by Richard on February 1,2010 | 03:44 PM

    wow! it always frustrates me when i hear things like this. although i'm happy because of the research that has been done as a result of her cells, the fact that they didn't even contact the family to inform them about what they were doing or pay them years ago is just wrong. this is just another case of poeple being taken advantage of because of their lack of knowledge. great piece lady!!

    Posted by rafaela mccoy on February 1,2010 | 03:44 PM

    I think this story is remarkable, so many people bless thanks to this lady. Also the picture posted on this story it's pretty much beat up, it should be fix before is too late, I will like to fix it for the Lacks family so they may enjoy this memory forever. Totally free.

    Posted by Lily on February 1,2010 | 03:44 PM

    I am not sure if the family is entitled to a bunch of cash as a result of those cells used. Those who donated their body to science have also similarly contributed to science over the years. Their family was not expecting some windfall as a result. The legacy of this woman is evident in the breakthroughs that the scientists found as they researched using her line of cells. The cells were not the breakthroughs no more than patient zero is responsible for a cure for a disease, it would not have happened without the educated and driven men of science. Her cells were no more than specimens in a petri dish. An interesting story none the less.

    Posted by Michael Herring on February 1,2010 | 03:44 PM

    I would agree with most of what you've stated, however understanding the history of this country when it comes to African Americans and White America, especially in the 1950 when it was not uncommon to be rejected from entry into most businesses and the door or seat one could set in had Back as a first name. I would tend to lean toward that there was some neglect on the part of the quote unquote white scientist that found a cheap way to fund his research. Did you the author discover if they even treated Ms. Lacks. I bet there was noting they could do for her and she died at home six months later.

    Posted by Darna Young on February 1,2010 | 03:44 PM

    I can't wait to read the book, and wish the best for the Lacks family.

    Posted by fasufoujin on February 1,2010 | 03:44 PM

    It goes to show you they still like to still the black race ways and secrets of life for there(the powers that be) own personal use. Why don't they share these outcomes as soon as it happens.

    Posted by Deric A. Rogers on February 1,2010 | 03:45 PM

    This is the most interesting piece I hae ever read, especially knowing that this is a black woman. I am going to try to track the book down as soon as possible.

    Posted by Joy Ammons-Hoy on February 1,2010 | 03:45 PM

    I agree someone owes Henrietta Lacks family alot of money. This would make a interesting story, I'm interested in hearing more!

    Posted by Chandra on February 1,2010 | 03:45 PM

    I can see why this stuck to you! I couldnt believe this as I was reading it. Very interesting indeed, I would love to read this Book, the knowledge that you can get from this information is diffenately something that should be passed down to our younger generation. I congradulate you!! AMEN

    Posted by kelly rock on February 1,2010 | 03:45 PM

    that was interesting. pretty cool i really want to know more!!

    Posted by Angelie on February 1,2010 | 03:45 PM

    wow!!!

    Posted by mckinley wood on February 1,2010 | 03:45 PM

    Encouraging, your determination and interesting regarding the continued life of the cells. I hope that her family does benefit is some way other than scientifically. Grief is hard to bare, especially for Deborah not having known her mother.

    Posted by norene holliday on February 1,2010 | 03:45 PM

    WHY IS EVERYTHING ABOUT $$$$$$$. PLENTY OF PEOPLE DONATE AND GIVE DIFFERENT THINGS FOR SCIENCE. WHY IS HER FAMILY DUE ANY MONEY FOR THEM TAKING CELLS FROM HER? THATS WHAT IS WRONG WITH THIS COUNTRY

    Posted by SHAME ON ALL!!!! on February 1,2010 | 03:45 PM

    Why hasnt Opra or Dr.Oz Gotten a hold of this? This deserves more coverage & explanation?

    Posted by Ray Reese Sr. on February 1,2010 | 03:46 PM

    Sorry but you aren't owed any money for something like that.
    Times were different back then, and she was being treated for a disease. Cancer cells also don't die that is why they are so deadly, they continue to multiply and consume your bodies energy.

    Posted by What the heck on February 1,2010 | 03:46 PM

    I had cousins who were used in the Tuskegee Institute Alabama experiment. They were told that they were going to Tuskegee to be treated for gonorrhea. Not until the Tuskegee story came out later did we know what had happened to them. (two of them female)

    Posted by Marjorie Pettway-Harlin on February 1,2010 | 03:46 PM

    This is very interesting and I, too, think this story would make a wonderful PBS documentary - maybe for next year's Black History month.

    Posted by Penny Ramos on February 1,2010 | 03:47 PM

    Why does The word racist always has to come up just because of her color, Do people realy think that the reason he took her cells was because she was black? Was it wrong that she helped cure polio and many other diseases? I do not believe it is wrong to use cell samples to studie and make vaccines with. People are just too paronoid, no one is going to secretly clone you get real. If someone was going to cloan somebody they would want to have a comparison, you would be told and know about it.

    Posted by Dave on February 1,2010 | 03:47 PM

    Im jus speechless! There are no words to say but WOW!

    Posted by Tanishia on February 1,2010 | 03:47 PM

    Not only should the family get the financial compensation due them, Henrietta needs the recognition for her contribution to medical science. I wonder how she would feel knowing she has made such an impact in the world.

    Posted by Cindy on February 1,2010 | 03:47 PM

    the world needs more people like you to tell a TRUE STORY. Thanks for sharing. Give us updates on how the research proceeds and when the family gets taken care of financially. They need to be compensated with free health insurance for the rest of thier lives!

    Posted by Sandra on February 1,2010 | 03:47 PM

    Here's a link for the book: http://www.amazon.com/Immortal-Life-Henrietta-Lacks/dp/1400052173/ref=sr_1_1?ie=UTF8&s=books&qid=1265056953&sr=8-1-catcorr If that doesn't work, it is called "The Immortal Life of Henrietta Lacks" It is on Amazon.

    Posted by Tony L on February 1,2010 | 03:47 PM

    I found this very interesting. Finding a way that it can happen that everyone's okey with,though, might be impossible, because humans never agree.

    Posted by Sarah on February 1,2010 | 03:47 PM

    very interesting article, makes me wonder what is going on in the world today. im a jamaican so im wondering if these things happen in jamaica also????

    Posted by saiyda brown on February 1,2010 | 03:48 PM

    Very interesting article, a must-read for me when I saw the headline.

    Posted by David Atkins on February 1,2010 | 03:48 PM

    wow. i have never heard of something like that. quite amazing!

    Posted by Carly on February 1,2010 | 03:48 PM

    It should be noted that scientists DO know why her cells are immortal. HeLa cells are cancer cells obtained by Henrietta's cervix, which was cancerous at the time and all cancer cells (by definition) are immortal---meaning if the cells are provided with a suitable medium (i.e. nutrients) they can survive forever. Cancer cells are immortal because they circumvent genetic functions that, in healthy cells, regulate gene proliferation and keep the cell from dividing and growing uncontrollably. At the genetic level, we believe this is in part due to the fact that cancer cells have the ability to extend the telomeres of their chromosomes. The shortening of chromosomal structure occurs in every human being (mortal) and is what we now believe is responsible for contributing to old age. Cancer cells experience no chromosomal shortening and thus, do not age.

    Posted by biochemist superstar on February 1,2010 | 03:48 PM

    I can undserstand this story and the ,and the wanting to know exactly how it could have happen. My grandfather was in the Tuskegee Study as how one race reacts to medicine and another does not. It just happen that they didn't give him the right medicine. We know that someone has to help with discoverie,but I think the families that are left behind should have better information.

    Posted by Sylvia on February 1,2010 | 03:48 PM

    I am 81 years old and quite possibly, may owe part of my life as the result of the tests made by the parts of this woman. I am eternally greatful to her memory.. dale

    Posted by dale l bryan on February 1,2010 | 03:48 PM

    It has been long known exactly why her cells are immortal. Many cancerous cells are. Furthermore, there is no law that allows the family to lay claim to these cells. In fact there is a law strictly forbidding this! Since the family does not own these cells, they cannot profit from them. (Unless of course, they were to use the cells for their own research!)

    Posted by Larry Pierce on February 1,2010 | 03:48 PM

    Really great piece. Love the humanistic side of science and literature!

    Posted by Naomi on February 1,2010 | 03:48 PM

    Very interesting story. As a science major in undergrad school, I studied about the HeLa cells but never knew it was a person. This makes great Black history trivia.

    Posted by Walter on February 1,2010 | 03:49 PM

    This is an amazing story, but it just goes to show you that the company who has made billions of dollars dont care about the family in which the cells originated from. "If They Knew"...Great Finances should be paid to the family...And a public apology...Color is always a factor...

    Posted by shawnee on February 1,2010 | 03:49 PM

    I find that while this article is interesting and very fascinating there seems to be a bit of wrong doing. I am sure people do alot of things in the name of science, I just wonder when we draw the line.

    Posted by Christina Bush on February 1,2010 | 03:50 PM

    I have had many operations and any tissue cut from my body no longer belongs to me. For these people to feel they are owed money for this woman's cells is ludicrous. It's the Welfare mentality guiding these folks to always feel that the government owes them and now they have just taken it one step further to the medical community owes them money. While I sympathize with the old man not understanding anything about medical science the story told to him could have been "dummed down" to the point where he would not have felt that his wife was alive in a laboratory, etc. probably just by telling it like I did in my first sentence. Most smart people try not to talk down to uneducated people and in so doing just make matters worse. I was involved in sales for almost 3 decades and I would talk differently to people after I sized up what I needed to do to truly make my customer understand what I needed to tell them so they could make a decision what to buy to have it do what they wanted it to do. It's the same thing for anyone dealing with the public in that to be an effective communicator you have got to dumb down in a non-condescending way if needed so you can explain things to people of all intellects. Most very smart people have no clue how to communicate with average people and would run away before trying to talk to the uneducated. Dumbing down speeches is as American as apple pie and politicians pay speech writers big money to dumb down their ideas to sell to the American people. I have always said that we should never underestimate the stupidity of the American Public.

    Posted by Bob Beard on February 1,2010 | 03:50 PM

    Good educatioinal instrument. I am sure it is used in med school. Now that this information is know...is the family compensanted and what is it about Heneretta that makes her cells special enough to advance our medical team so many years. One person can make a difference. She proves that! Great peice, thanks for the info.

    Posted by Debra Rudolph on February 1,2010 | 03:50 PM

    I think those immortal cells are telling us about our origins and that we were supposed to be immortal. That an Africn American womans cells are being used to achieve so much is wonderful.

    Posted by Lovie on February 1,2010 | 03:50 PM

    money, money, money , money, money.....is that all people care about? yes her family should have been asked before the scientist took her cells...but if they had asked and she said yes (which she probably would have)....its called "donating" to science for the better of mankind altogether. i thank her family for her cells and all the advancements that have come from this. truely an amazing story, but im not sure about compensation for the family....would they have paid for them in the first place if they asked? i dont think so.

    Posted by jeremy on February 1,2010 | 03:50 PM

    Great work Rebecca Skloot! I will share this with my five children. Not just the story about cells but how this story you first heard about when you were only 16yrs of age drove you to want to learn more about Henrietta Lacks and how it gave a little peace to daughter Deborah. Bravo!!

    Posted by Ida on February 1,2010 | 03:50 PM

    After the Billions of dollars made from this woman and her family, what compensation has been given to them?? Are they still being allowed to live in poverty? I assume more money is going to be made from this book, so how much of the proceeds are going to the family???

    Posted by Tommy Franks on February 1,2010 | 03:50 PM

    great piece, nice to see something intelligent, thoughtful and interesting gaining so much interest!!!! though yes, in terms of ethics, this was very wrong they should have asked.

    Posted by sara on February 1,2010 | 03:50 PM

    some one needs to step up and compensate this poor family. If it was not for HeLa cells, our world would be less successful in the bio world!

    Posted by Sandy on February 1,2010 | 03:51 PM

    WOW!!! I'm amazed, how everything is becoming so about $$$... in this world. nice story, I would like to read more about it!

    Posted by Martha on February 1,2010 | 03:51 PM

    Whoa!!! This is interesting. IOmmoratl cells form 1951!!! wow. that amazing!!!

    Posted by Liz on February 1,2010 | 03:51 PM

    Reparations! Reparations!

    Posted by Jacob Farmer on February 1,2010 | 03:51 PM

    Well, since they took and sold pieces of her without her concent to sell. I believe this family is owed some financial compensation. Then any future rights to stories and sales.

    Posted by Cowboyinvestorx10` on February 1,2010 | 03:51 PM

    Amazing!!! I am going to get the book. Hope the family got some money.

    Posted by Bill on February 1,2010 | 03:51 PM

    Who gives anyone the right to take cells, without permission from the family and use them the way these were used? I agree someone owes this family alot of money and a big apology.

    Posted by N Daley on February 1,2010 | 03:51 PM

    With all due respect, I don't think this family should get paid. It's not like she was the one making all the breakthroughs and doing all the tests and research. They were just cells that were taken to be studied. If I blew my nose and threw it in the trash and somebody found it and used it to do research, I wouldn't expect to make money off of it. Still, it does make for an interesting story.

    Posted by Tim on February 1,2010 | 03:52 PM

    thats what i call research..i like the story

    Posted by Haman on February 1,2010 | 03:52 PM

    Black History .. I read this article in Oprah This Month now main stream America is catching up

    Posted by Tracy on February 1,2010 | 03:52 PM

    I take offense at the use of the word 'inanimate' to describe fruit flies. They are very much alive, as are mice and monkeys. I work in a neuroscience lab at Johns Hopkins, and I understand the value of working with live animal models, but I think it is crucial to remember that these creatures are living, breathing, sometimes sentient beings that deserve our respect and gratitude.

    Posted by Arthur on February 1,2010 | 03:52 PM

    I found it between $10 and $15 on amazon.com

    Posted by mike on February 1,2010 | 03:52 PM

    Your article makes me want to read your book, and I sincerely hope the monetary issue is rectified.

    Posted by Gary on February 1,2010 | 03:52 PM

    Verry interesting, I had not heard of these cells before... thinking of buying the book to know more about this peson and her history.

    Posted by Roni on February 1,2010 | 03:52 PM

    a very good story...

    Posted by kreng on February 1,2010 | 03:53 PM

    Man... You just don't get it by writing this piece. It shows how arrogent and self serving the biologists and pharmacy companies are with the human cultures they take and use for their profit- and human good. This family, who many are destitute, is owed huge amounts of money for their un-knowing gift to science-especially since these cultures are being sold -presumably around the world!!!! Get this family this money it is owed. None of this would be legal with today's laws.

    Posted by Ralph on February 1,2010 | 03:53 PM

    Just what we need, people that live forever.

    Posted by toejoe on February 1,2010 | 03:53 PM

    The sory is very touching and the scintific fact si also amazing. Everybody who is interested in cellular biology and genetics(even from a layman's point of view),should read Matt Ridley's "Genome". This is how I first heared about Henrietta Lack.

    Posted by Alina on February 1,2010 | 03:53 PM

    The book can be bought from: http://rebeccaskloot.com/the-immortal-life/

    Posted by Marko on February 1,2010 | 03:53 PM

    This explains a lot of things. Like how they think we're closely related to the primates. They need to take samples from Dolph Lundgren as a comparison before they make unscientific statements.

    Posted by Karen on February 1,2010 | 03:53 PM

    A doctor took a sample with out her knowing it? Wow! That seems unethical to me. I don't care how much anyone thinks anything is for the "greater good". A violation of one of our rights is a violation of all of our rights. The real greater good is the protection and respect of each of our rights, not the ambitions of someone taking something that is not theirs to begin with. Then the DNA was used for all kinds of expirements? Sounds like the Lacks family is due a settlement.

    Posted by JLP on February 1,2010 | 03:53 PM

    VERY "INTERESTING STORY" LOOKING FORWARD TO THE BOOK! ALL IT TAKES IS ONE PERSON TO MAKE A DIFFERENCE.

    Posted by johnerock on February 1,2010 | 03:53 PM

    i really enjoyed the piece. very interesting topic indeed!

    Posted by madison on February 1,2010 | 03:53 PM

    Wow! This definately caught my interest. I'm putting this in my list of books to buy.

    Posted by Cyndya on February 1,2010 | 03:53 PM

    I Like history and I love this story but I hate the Idea that money was involved, in my opinion those cells should never have been sold, when we work as a whole to save the lives of all, money should never have entered into the equation but since it has, by the power of science, then shame on you and give what that family should of had, with interest. What a miracle to have cells that are immortal, and to think instead of sharing it freely it was sold. I don't think it was about Black or white, it was about making a buck, I hope you give that family a good portion of the money you are making from this book

    Posted by Maria DeCosta on February 1,2010 | 03:53 PM

    The book is titled The Immortal Life of Henrietta Lacks by Rebecca Skloot :o)

    Posted by Sunshine on February 1,2010 | 03:54 PM

    This is a very interested story, and to know that this black woman has a history that is powerful is unbeliveable. I hope her family knows how important their mother was, and that they too has powerful gene as will.

    Posted by gina pope on February 1,2010 | 03:54 PM

    How wonderful it is that Henrietta's contribution to the world is finally getting accurate recognition. I agree with another comment made, her family should get great financial compensation for this. Rest in peace Henrietta, your contribution to humanity is immense.

    Posted by Lynda on February 1,2010 | 03:54 PM

    So did the family get their fair profit from this? Also it brings up a good point, how things can go wrong. It stated in the 8th paragraph" It turned out that HeLa cells could float on dust particles in the air....." So what harm has been done to society because of these testing labs? Such as the controversal H.I.V. Aids epedemic? I think because of people wanting to become famous and filthy rich things can become out of control, don't you? sure there does need to be a cure for things such as cancers however there comes the consequences of missused tissues, accidental useage such as in a chemistry lab where things will blow up, unfounded territory. Are we making ourselves sick, are you making us sick for your own greed?

    Posted by Nancy on February 1,2010 | 03:54 PM

    I am 51 years old and never knew what the significance of HeLa cells was.

    Posted by Lucinda on February 1,2010 | 03:54 PM

    The book is called " The immortal life of Henrietta Lacks" by Rebecca Skloot. I bought my copy at Barnes and Noble. Awesome book.

    Posted by Christine on February 1,2010 | 03:55 PM

    I agree someone owes Henrietta Lacks family alot of money. This would make a interesting story, I'm interested in hearing more! Posted by Chandra on February 1,2010 | 12:45PM FOR WHAT?

    Posted by bruce becker on February 1,2010 | 03:55 PM

    wELL I THINK THIS FAMILY SHOULD HAVE SOME BACKING, AFTER ALL THIS RESEARCH, AFTERALL THIS IS GOING TO BE A FANTASTIC ADVANCE FOR MANY YEARS TO COME ???

    Posted by MIMI BALL (MARIE) on February 1,2010 | 03:55 PM

    Very, very interesting. I've pre-ordered the book on Amazon. It comes out tomorrow.

    Posted by Andy H on February 1,2010 | 03:55 PM

    dis is so cool!!Most amazing thing i ever heard!! must buy the book and how much is it ??

    Posted by Heena on February 1,2010 | 03:56 PM

    This is an amazing story, yet interested and should be told. I think it will make a fantastic book,even a great documentary. I am sorry that the family wasn't told of this earlier. Where as the medical field broke history a trust fund could have and should have been established for Henrietta Lack siblings and kids,someone should have been compensated.

    Posted by Michelle Lewis on February 1,2010 | 03:56 PM

    Wow!!!!!this is such an amazing story. In as much as I am happy that this much has and is being achieved in science because of this woman, I still believe the family should be compensated.

    Posted by Asana Amadu on February 1,2010 | 03:56 PM

    Releasing this info about this woman could in no way affect this family physically or negatively. Therefore, the law says if she gave her blood to people, especially in the fifties, they can use it and call it what they want, just like organ donors. I know if my cells were used to help the world no amount of money in the world could buy that good feeling.

    Posted by bill on February 1,2010 | 03:56 PM

    I would like to know how to get in touch with someone that could help me find out what happened to my grandfather after his death . He was hurt in a car accident in the late 1920's . I have his obit . He died ten days after the accident from a broken back . The doctor's asked my grandmother to sell them his body for research , but she told them no . But his body dissapeared from the cemetery and there is no record of him being buried where he is supposed to be . My uncle years ago wrote a letter to someone and got a reply giving the date of my grandfather's death and the date of his burial as being over 20 years apart . The family felt there was nothing they could do about it . The letter has long been lost . I have tried to find out where he is buried and have been told the same thing as my grandmother , that they have no record of him being buried where he is supposed to be . I would like to know where he is buried so that I can at least visit his grave and maybe leave some flowers . Can anyone out there help me with this ? His name is Henry Clay Boone and The famous Daniel Boone is his fourth great uncle .I have documents to support this . I think it is a shame not to know where he is or what happened to him . Nancy

    Posted by Nancy Salisbury on February 1,2010 | 03:56 PM

    Still the family needs to be compensated for the cells. This is a huge injustice.

    Posted by Scientist on February 1,2010 | 03:56 PM

    Very interesting story indeed! I had never really heard of immortal cells until now. I have one question though, did Henrietta's race made a difference in the immortality of her cells?

    Posted by masnoh wilson on February 1,2010 | 03:57 PM

    One place the book is for sale http://www.amazon.com/Immortal-Life-Henrietta-Lacks/dp/1400052173

    Posted by Joe broers on February 1,2010 | 03:57 PM

    The lawsuit was Moore v. Regents of the University of California. The Supreme Court found that an invidividual has no property or ownership interest in their cells or biological tissue after they are removed or discarded-- So Mrs. Lack's family recieved nothing. This may sound unfair at the outset, but think about the practical problem of determinig who "owes" Mrs. Lack's family compensation-- and how such a decision would put up barriers to medical research.

    Posted by Beth on February 1,2010 | 03:57 PM

    Doctors have always used parts of people for research without their permission,especially African Americans. I hope the family is compensated.

    Posted by Nicole on February 1,2010 | 03:57 PM

    what a cool story. So did the family ever get any money? So when u said they used her cells for cloning did you mean they cloned her?

    Posted by elijah hills on February 1,2010 | 03:57 PM

    How interesting, so many years later her cells are being used and I agree her family should get some restitution.I continued success in the research.

    Posted by Lana on February 1,2010 | 03:57 PM

    The fact that the cells gave rise to some of the most groundbreaking medical discoveries since the 50's does not change the fact that they were stolen. The fact that no effort has been made to compensate the family testifies to the callousness of researchers responsible for the original theft, and is an indictment against subsequent researchers who have benefitted.
    To steal one's ideas in the reasearch setting is grounds for virtual banishment from the lab. Yet nothing was done when researchers stole part of a persons body.
    I hope the family gets a nice chunk of the billions that these thieves have shamelessly and unapolegetically profitted at the expense of their relative.

    Posted by Gary Caldwell on February 1,2010 | 03:57 PM

    Racist white scientist? They did odd thing to soldiers, poor people and people in general back then. Their definition of ethics was lower and at times higher than ours is now. Look at it from all sides and try to look at it from all periods of time. Of course saying racist white scientist does sell more books.

    Posted by flatlander on February 1,2010 | 03:57 PM

    She didn't donate her body to science they took a piece of her, so yeah the family is entitled to money, lots of it. Once again American taking advantage of the minority.

    Posted by Kim on February 1,2010 | 03:58 PM

    This is so crazy, I never heard anything like this before. I want to know more about this and keep updated with it.

    Posted by MarkValdez on February 1,2010 | 03:58 PM

    cool..? jk good story

    Posted by niikki on February 1,2010 | 03:58 PM

    GREAT story, need more info on the book, want to know more,more.

    Posted by on February 1,2010 | 03:58 PM

    Fantastic Article, after reading it and several comments about it I was saddened to hear of several people just thinking of dollar signs. Typical though, someone out to make an easy and fast buck. We have so much of that in the world today. My family wasn't exactly poor, but my father worked very hard to feed us 6 children. We had food, some clothing that had to last a year or more,that was it, we were thankful for whatever the good Lord gave us. Now for Henrietta Lacks, what a legacy this young lady has unknowingly left for herself and for her family.

    Just think of all the lives she has saved, if not for the research of her cells, alot of people, me and you may not have possibly been here today. From now on when I hear of scientific and medical breakthroughs I will think of Henrietta Lacks, and thank God for putting her on this earth. As another commentor stated, this would make a wonderful film or documentry, it would be great to see the with proceeds going to the family. I am sure the scientist was not thinking of dollar signs when he took the tissue sample from her tumor, he was thinking hopefully about saving lives, and seems as though that was true. I will bye the book when it is available.

    Posted by Terry Tate on February 1,2010 | 03:58 PM

    Where can I buy the book? Very interesting!

    Posted by Terri on February 1,2010 | 03:59 PM

    First she didnt donate they stole a big diffrence ---A doctor at Johns Hopkins took a piece of her tumor without telling her --- she was alive.. !!!!! Its diffrent if some one gives their permission.. Sick of people profiting of others..

    Posted by Jenna on February 1,2010 | 03:59 PM

    Name of the book is.....The Immortal Life of Henrietta Lacks by Rebecca Skloots...i found this to be a very interesting artical and want to buy the book for me and my daughter to read...my daughter is finishing her Masters in Nursing and then on to get her Nurse Pract. im sure she will find this as interesting as i do...thank you

    Posted by pamela hamm on February 1,2010 | 03:59 PM

    Does this mean that cancer cells are airborn? it seems that this is true according to the artical. Where can I find out more information?TY

    Posted by Esther on February 1,2010 | 03:59 PM

    Reading this shore article really made me interested in reading the book as well.

    Posted by Sophia on February 1,2010 | 04:00 PM

    Cervical cancer is so bad and it must have been horrible in 1951 with no options that science has brought us today. I will bet if Henrietta knew all the things her cells had accomplished she would be pleased. I hope her family did get some compensation for the wonderful things their relative helped bring about.

    Posted by T C Hentschel on February 1,2010 | 04:00 PM

    Extremely fascinating!

    Posted by Michelle on February 1,2010 | 04:00 PM

    Grrrr.....these people should pay for what they stole not sell it without a thought about the people who are connected to these genes and help EVERYONE.>:( mad face

    Posted by Stan :D on February 1,2010 | 04:00 PM

    As a family member of a loved one who died of polio in 1940 long before the vaccine was developed, this especially touched me. Like so many others, I want to read this book, and I congratulate the author for her dedication and research.

    Posted by Roberta Browne on February 1,2010 | 04:00 PM

    It provides an interesting angle to the Biblical ages of many people mentioned in the Old Testament. Before, we couldn't comprehend how people could live for hundreds of years. We dismissed it as fairy tale nonsense. Now, it provides a clue that it very well may have been possible after all.

    Posted by Izzy on February 1,2010 | 04:00 PM

    Very interesting story!

    Posted by Nasim on February 1,2010 | 04:00 PM

    Fruit flies are NOT inanimate. Specism is even worse than racism. Life forms who are smaller than humans are yet larger than other life forms; scientists must cease regarding humans as the rulers of the Universe.

    Posted by Judith Shipstad on February 1,2010 | 04:01 PM

    Why does everything have to center around money? If I knew my body could help with research and development to find a cure for diseases, I would gladly donate my body after I'm done with it. That's the problem with people today, money hungry!!
    How about doing things out of the kindness of your heart.

    Posted by lac on February 1,2010 | 04:01 PM

    We touched on this in my bio class. I hope Henrietta's family was eventually compensated.

    Posted by Derek on February 1,2010 | 04:01 PM

    book comes out tomorrow, available at bookstores.

    The Immortal Life of Henrietta Lacks
    by Rebecca Skloot
    Crown Publishing Group
    2010

    Posted by n c on February 1,2010 | 04:01 PM

    I moved to Baltimore in the 70's and worked at Hopkin's for several years. I heard lots of stories from the residents how Hopkins would experiment on people without their knowledge.there is a distrust from the people in the community. I hope the family get some vindication.

    Posted by dorothy on February 1,2010 | 04:01 PM

    I am a scientific researcher, and understand the complications involved with morality and research. For example, such issues are well illustrated in stem cell research. However, one has to realize that when a person simply submits cancer cells to scientific research, they would have no right to any profit from the research anyways as their identities would be hidden immediately, even to the researcher. It is like blowing your nose and saying that anyone who ever makes any discoveries from your boogers owes you money from that. The family should simply be proud that they have had an integral part in the scientific advancement of our race. I understand it is frustrating that scientists did not obtain her permission, and it is also frustrating that scientists had such horrible lab techniques that they were cross contaminating samples, but that is the situation that existed during that time. While it was wrong for them to do that, it is just as morally decrepit for the family to want monetary gain from the situation. Even if she HAD volunteered her cells, she would STILL not be privy to any money gained from research regarding her cells. The world is simply ruled by greed these days...

    Posted by Andy on February 1,2010 | 04:01 PM

    I agree with the thought of her cells floating around into other research is pretty scary. We need to understand that while Mrs. Lacks was black same type of things were done to the whites and others, thus making this a non-racial issue.No one thought one thing about permission only that certain diseases need research and cure. When this was spoken of on the evening news they mentioned that her family was very upset but now are proud and happy that Mrs. Lacks was able to contribute. So the above article neglected to mention after the family thought about it now.
    Instead of all that money give her whole family any type medical treatment for life.

    Posted by Peg Davis on February 1,2010 | 04:01 PM

    What a stunning story!! What a hero Henretta is!!

    Posted by Denise Ragland on February 1,2010 | 04:02 PM

    WOW!!!!

    I would like to say Thank You for such an inspiring article about this Beautiful Black Woman named, Henrietta Lack. Today I learned something I NEVER KNEW.

    Kay

    Posted by Kay F. McCray on February 1,2010 | 04:02 PM

    This article has really opened my eyes at whats going on around us. I have a new found respect for cell researches and studies. Thank you Ms. Skloot.

    Posted by Roslyn Rankin on February 1,2010 | 04:02 PM

    The book is called, The Immortal Life of Henrietta Lacks by Rebecca Skloot. It will be available as of tomorrow, Feb 2, 2010. Depending on where you get the book it can run from $15-$25. This is a great story and I will be reading the book.

    Posted by Dee on February 1,2010 | 04:02 PM

    I agree that those who donated organs to medical science out of their generosity chose to do so of their own free will and no monetary compensation in needed.

    But in this case, the took a part of her body and used it w/o her permisson. If they took your eyes out while you were sleeping and made money from it and never told you about it, it would be no different.

    A part of her cervix is as much a part of her sacred body as her eyes would have been. If we do not own our body, what do we own???? if they cut off a piece your genitals secretly, I woulder how you would feel.

    The family shoud be compensated.

    Posted by charlie on February 1,2010 | 04:02 PM

    Why would the family be entitled to compensation? Sounds like cashing in on their mother's misfortune to me.

    Posted by Rogan on February 1,2010 | 04:02 PM

    Good investigation but needs more sensitization or else people will frown at culture.Not everyone will collect it illegaly like the doctor.

    Posted by Allieu Tommy on February 1,2010 | 04:03 PM

    I don't think the family got any money. There was some court ruling several years back where some guy tried to do pretty much the same thing with cells taken from his appendix I think. Basically the court ruled once cell samples are removed from your body they are no longer yours.

    Posted by CDR on February 1,2010 | 04:03 PM

    I too want to know if the family received any money from the doctors who stole and sold her cells?

    Posted by Marcus on February 1,2010 | 04:03 PM

    I think what happen to Henrietta and her family is very unfortunate, by taken a part of her body for experimental use without her knowledge was quite wrong and the families should be compensated, not because they are @ a 3rd grade interlect or poor and homeless but because it is the correct thing to do. I agree collecting cells So much of medicine today depends on tissue culture. HIV tests, many basic drugs, all of our vaccines however, patients have the right to know what is being done to there bodies so, they can make informitive, consciention decision along with there families, and Dr's have an obligations to inform patients of whats going on with them, don't just take a part of someone for scientific use then justify it 25yrs later and say its ok to determine medical issues, and not because someones, family as it may is not educated bypass them. I am greatful that this information is written and it makes me much more aware, to myself and people that I know, stealing body parts as we know is a vey big business.

    Posted by annmarierowe11@yahoo.com on February 1,2010 | 04:03 PM

    As a nursing student I am always looking to learn more and I really feel that was accomplished with this article. I would also like to say thanks for getting my attention because I never read the online stuff and I never usually comment, so GREAT JOB and I hope the family has received what they genetically should!!!

    Posted by B.Wilson on February 1,2010 | 04:03 PM

    http://search.barnesandnoble.com/booksearch/isbninquiry.asp?r=1&ISBN=1400052173

    Posted by Shalindria on February 1,2010 | 04:03 PM

    Wonderful, and thought provoking!

    Posted by chelseasekely on February 1,2010 | 04:03 PM

    People are ridiculous. The family doesn’t deserve money for the “use” of the cells. Just because it has been helpful and the family is/was poor isn’t a grand excuse to wring money out of some company. The original doctor removed CANCER cells that were part of a tumor. If you have cancer and have a tumor removed, are you going to ask to keep the blood mass removed from you? I don’t think so. All that happened was that someone took medical detritus and made it useful.

    Posted by Jon on February 1,2010 | 04:04 PM

    What some of you fail to grasp is that the cells were cancerous and were to be removed and disposed of anyway. Should the doctor have asked permission? Yes, he should have, and Henrietta would most likely have said yes. Folks were that way back then, not always worried about how much money they could get, but willing to help if they could. Today, everyone has their hand out and the first words are usually "What's in it for me?" What was she going to do? Tell them "No, but the cells back!" She may not have known it then, but she has helps tens of thousands, if not millions, with that little piece of tissue that was most likely going to end up in the trash bin.

    Also, the reason HeLa cells grow rampantly is that they are cancerous, and by the very definition of cancerous their growth is mutated. And, yes, they will contaminate pretty much any other culture they get anywhere close to. We always had to take special precautions when doing culture work with them, before, during and after, in order to prevent cross-contamination. Sometimes it still happened, not matter what precautions we took. They are healthy little buggers.

    Posted by Kasey on February 1,2010 | 04:04 PM

    nice.. i don't know that there's a immortal human cells coz' i've only tried was culturing the microbes.. i'm also aware of tissue culture but not that much..
    nice i think i need to study that also..

    Posted by lea on February 1,2010 | 04:04 PM

    Science has made giants steps in cell research, it is for the common good to be able to establish positive cures for certain diseases. The family certainly should be given monetary awards for the use of Mrs. Lack's cells since no permission was given.

    Posted by W. Lee on February 1,2010 | 04:04 PM

    What an interesting story. I thank God for the cells of HeLa. I would want to read this book from the 1st page to the last. Someone help me please!

    Posted by Roberto Chuka on February 1,2010 | 04:04 PM

    I read an excerpt in Oprah's O Magazine; it was great. So, I ordered the book from Amazon.

    Posted by Kim on February 1,2010 | 04:04 PM

    In all fairness, I'm sure Henrietta would want her family taken care of for the contributions her cells have made, especially since they were taken without permission.

    If it were me I'd be delighted to know how so much good has come from a genetic accident and wouldn't care about whether permission was asked for, however bequeathing something to my family would be the right thing to do.

    Posted by Jeff on February 1,2010 | 04:04 PM

    The family should have been notified. The family should be paid. If for no other reason except, there WAS MONEY MADE FROM her cells. It is sad that it comes down to money, BUT they still need the family for further cell research it seems, so the company needs to pay them for the past use of Mrs. Lacks' cells, and for the present/future request of using her children, grandchildren etc. cells.

    Posted by tiny on February 1,2010 | 04:05 PM

    How can we trust our own doctor's. I think Henreitta should have knownabout her cells and her doctor should have had her permission beforehand.

    Posted by lizzy on February 1,2010 | 04:05 PM

    I think that it is awesome that Skloots wants to tell Mrs. Lacks story and she is right, without cell research we would not have the information and vaccines that we have today.

    Posted by Tisa on February 1,2010 | 04:05 PM

    A link to Amazon to order the book. Looks like it gets released tomorrow, February 2nd.

    http://www.amazon.com/Immortal-Life-Henrietta-Lacks/dp/1400052173

    Posted by Meg on February 1,2010 | 04:05 PM

    I'm interested in reading the book because I'm hoping there are more explanations for the longevity phenomenon. Do other cell cultures die off automatically? Was something special done to these cultures? How does the information that these cells were originally cancerous factor in there? I'm now extremely motivated to track down and read this book! Thank you for the report.

    Posted by MakBeth on February 1,2010 | 04:05 PM

    it amazes me at what science has been through in the past 50 years. i myself am grateful for cancer research. the first one that mentioned that the family is owed money...you're very, well, let's just say ungrateful for what you have in life it seems. they may be owed i'm not sure. someone else stated what about the others that dedicated themselves to science after death....they don't get paid either. we who live in the united states are some of the most money hungry people on the planet and yet.....you lack in compassion for even yourselves. think of a family member with cancer that needs medical help. without this woman in this article where would they be? where would my mother be? where would i be instead of talking to you now?

    Posted by mthomas on February 1,2010 | 04:05 PM

    Nice piece!!! Very interesting!...

    Posted by Xty on February 1,2010 | 04:06 PM

    Simplemente facinante, Dios Bendiga a Henrietta Lacks

    Santiago Montero
    San Jose Costa Rica

    Posted by Santiago Montero on February 1,2010 | 04:06 PM

    Where i can get this book. This story is very interesting,and I want to read it.

    Posted by Jose Rivera on February 1,2010 | 04:07 PM

    Did they really have to start it off as "poor black tobacco farmer"?

    Posted by Mason on February 1,2010 | 04:07 PM

    I'm amazed that someone hasn't suggested bringing a lawsuit against Johns Hopkins.

    People are usually more interested in hard cash than medical achievement.

    Posted by High Jarce on February 1,2010 | 04:07 PM

    Facinating story. I don't know about the monney issue, how it would be figure and paid by who but possible some lawyer{s} might want o investigate and possible , if they feel there is some precedent and reality of how to and who to collect from , will do it on a contingenxcy basis. In this case the courts would decide.
    For so many saved from polio and for those who may be saved from other disease, thank you to the doctor who sent the tissue sample on to another Lab , for that unselfish act a lot of people are alive today and possible in the future too as new cures for other diseases are found out by useing these special cells.

    Posted by Nate S on February 1,2010 | 04:07 PM

    If her super resistant cells never died, why her cancer cells gained the battle? What's the ability or the capacity of the cancer cells to destroy such resistant HeLa cells?

    Posted by A. Acosta on February 1,2010 | 04:07 PM

    The books title is "The Immortal Life of Henrietta Lacks". It will be released on Feb. 2, 2010.

    Posted by Jim on February 1,2010 | 04:08 PM

    It's funny how the past, present, and future of cell research is revolving around a beautiful black Queen go (hela)

    Posted by ebony on February 1,2010 | 04:08 PM

    God does indeed work in mysterious ways. This is just amazing.

    Posted by Karen on February 1,2010 | 04:09 PM

    If not for a single cell or maybe a million cells, where would modern medicine be today. The gift that was made available through this womans personal suffering becauses of a disease that now haunts the world should not be rewarded with money. She gave more than money can buy. She gave birth to new life. He family should be proud and full of joy that God provided her with a special gift to the world and others should continue to give the gift. Tomorrow may give birth to yet a brighter day.

    Posted by C.B. Morton on February 1,2010 | 04:09 PM

    This article was very interesting but I had to comment on the part about the family getting their share of the money and how they were so poor but in the photo their mother has a mink coat on and looks very well dressed.. so Im wondering if the family had money at one time and wasted it and now that the research is known they came out off the streets to claim it. If that's the case they are greedy... Now if they said Wow my mother has become an inspiration for so many lives and we want to continue her legacy and donate some of the money we receive to Cervical cancer research than that would have been wonderful... Looking forward to the book :)

    Posted by diana C. on February 1,2010 | 04:09 PM

    I agree that the family is owed compensation. This is really interesting and I would really like to read this book.

    Posted by Michelle on February 1,2010 | 04:09 PM

    Very, very interesting piece. I just sat here, with my 13 year old son, and learned something, which is very enlightening. Thank you

    Posted by Saundra on February 1,2010 | 04:09 PM

    Incredible!!!! Thank You Henrietta, you have helped so many people,while science robbed you of your most personal posesion, the cells that were a part of your body.Who knows how many others suffered the same fate. I hope your family realizes what a great gift you have given to the world,and how much is owed to them. Your family and all generations of your family for the rest of eternity should not want for anything. But we all know that will never happen, the government will find a way to weasel out of it.

    Posted by Elvira on February 1,2010 | 04:10 PM

    I think if they took her cell without her consent and made millions of dollars selling polio vaccine and other medication to people; they have to compensate her children. It’s only fair.

    Posted by George Santana on February 1,2010 | 04:10 PM

    This is very interesting and want to know more but the family should be compensated now that it has sponed a whole industry that has proved invaluable to the world THE FAMILY should be PAID.

    Posted by Kevin Satterfield on February 1,2010 | 04:10 PM

    Generally, people *donate* their body to science. However, people are making lots of money off of the Hela cells and that these cells were taken without the participant's knowledge. I don't know what the laws were back in the 1950s, but, some sort of renumeration might be warranted. Or, the return of all of the cells to the family.

    Posted by Am on February 1,2010 | 04:10 PM

    Wow! its sick!!!!!!! lol well no one owes this lady the money because im sure she would have wanted it this way. This lady was brave and i want to read the book. TOOOOOOOOOOOOOOOOOOOOOOOOOOOO!!!!!!!!!!!!!!!!!

    Posted by nancy perez on February 1,2010 | 04:10 PM

    Definitely an amazing piece of history. Look forward to reading the book.

    Posted by Leticia on February 1,2010 | 04:10 PM

    So......shouldn't this story be about the scientist that developed the cells?

    Posted by Layla on February 1,2010 | 04:11 PM

    From my high school education, I have heard that tumor cells are essentially immortal because they turn off suppressors which trigger apopotis, or programmed cell death. While I read this article, I had a question about WHY H's case is so significant.

    Posted by Kitt on February 1,2010 | 04:11 PM

    I think it would be fairly good reading for most! Along the same line and as an eye opener,if you have the chance read NEXT by Micheal Crichton.It gives you some insite as to the ownership of such cells and genes whether you donate them or not to labs or others.

    Posted by John Robinson on February 1,2010 | 04:11 PM

    All cancer researchers know that cancer of all types are immortal. This is not a surprise anymore. It's about genetic expression, that when a cell divides, a strand of proteins called the telemere chain is normally shortened a little bit. When it gets shorter, the cell divides a little less perfectly, hence the aging. When a cancer cell divides, it's a perfect copy, though abnormal AND destructive enough to kill the host. The telemere chain is never shortened, and hence, the killer cancer cells never 'age'.

    This is common knowledge among scientists. Just google telemere and look around and read a little. This mystery has long been solved and is not a big deal anymore.

    Posted by Daniel Roberts on February 1,2010 | 04:11 PM

    This is an astounding story. I can't help wondering why it was not shared with the rest of the world. Of course, people are sensitive when it implies a sense of hiding the truth about an amazing BLACK AMERICAN WOMAN. What else are THEY hiding. You know who you are. Enough said about that. This book is a must read for all of academia.
    I am to say the least amazed.

    Posted by Carlos on February 1,2010 | 04:11 PM

    would this happen to anyone without us knowing?

    Posted by lissa on February 1,2010 | 04:11 PM

    This was very horrbile that science can take a person cells without premission. I think that the federal government and science owe this family muilt billions of dollars for taking this ladies cells.

    Posted by Dee on February 1,2010 | 04:12 PM

    This is such a wonderful piece. I never knew anything about immmortale cells and the fact that this womens cells are used for alot of thins today that help us with diseases, this is one cool story. i also hope that people, whoever and whatever race they may be, not make this into any racial story like people often do.

    Posted by Alyssa Martinez on February 1,2010 | 04:12 PM

    The one thing that distrubs me is that the previous writer said the family was not entitled to any money because of volunteering her cell, no where in this articile did it say she volunteered.

    Posted by NANA on February 1,2010 | 04:12 PM

    This story makes me sick. Just because something is useful does not make it good. I agree it was wrong for the doctor to take the sample from Henrietta's tumor without telling her. If he would have gotten her consent there would be no obligation for any money to be paid out. I wonder how much education Deborah and her brothers had. Hopefully it was above the third grade.

    Posted by Osbourne Cox on February 1,2010 | 04:12 PM

    Love it!

    Posted by Kimbely Bostic on February 1,2010 | 04:12 PM

    I loved the article and want to read the book.

    I disagree that it made the family look greedy. It is more about showing the disparity between the money the scientists made and how the family was living. I know if I lived from hand to mouth my whole life and found someone had been using me and my family to make millions, I would be angry.

    I am philosophical about the scientist making money. Look at the Tuskeegee Airmen case. Enough said...

    Posted by lakota silver on February 1,2010 | 04:12 PM

    I'm sure she is not the only person in this world that has immortal cells. Get over it.

    Posted by Shorty on February 1,2010 | 04:13 PM

    Not trying to heighten the racial issue, but...Sadly this wasn't the first and probably won't be the last time Blacks were used in experiments without their knowledge or consent. Blacks have been used as guinea pigs since slavery. Hopefully the family benefits as much as others have from this incredible woman's cells.

    Posted by Chrystal on February 1,2010 | 04:13 PM

    waw if her cells and part of her tissues lived on do u think maybe her organs counld hav also been immortal?

    Posted by Aneilia Missir on February 1,2010 | 04:13 PM

    awsome!

    Posted by ryan on February 1,2010 | 04:13 PM

    That horrible doctor removed a tumor and didn't pay her for it?

    Posted by bill on February 1,2010 | 04:13 PM

    Very Cool. Makes me want to learn more about cells.

    Posted by CA Dean on February 1,2010 | 04:14 PM

    I doubt that the scientist selectively neglected Mrs. Lacks when he was trying to treat her cancer. He probably took samples from tons of people before he stumbled on to the immortal cells. I also doubt any money is coming to the Lacks family. The statute of limitations would have long run out on most crimes or torts (conversion, invasion of privacy) concerning the theft of biological samples. If my cell samples helped cure peoples' illnesses I would be happy even if I wasn't paid for them.

    Posted by Jackie on February 1,2010 | 04:14 PM

    Michael Herring's bigoted comment that Henrietta's Lacks' "immortal" cells were not a breakthrough, & that the research on them was a breakthrough, are the legacy of the enslavement of African people. I'd like to note, Michael, there'd have been nothing to research if her cells were like those of everyone else. Hello!

    Posted by Loy Henderson on February 1,2010 | 04:14 PM

    Great story. Scientists and researchers frequently think they are saviors of humanity, but so much of medicine and science is accident. They don't have a clue about lots of things. As a researcher myself, I have seen many ugly things in Science and Research.

    Posted by bob on February 1,2010 | 04:14 PM

    Fay actually just made the comment "What great research this lady has done." She didn't do any research, the science community did. Get that straight people. Especially BOB ROC who said "the doctors were making millions off of their mothers cells. The doctors were making money off of medical advancements that they worked hard towards and studied for years to be able to accomplish. Come on people, use your heads. Neither the woman nor her family had anything to do with medical advancements that came from these cells which could have been taken from anyone. The statements made to the contrary are made by ignorant people with no integrity.

    Posted by Rich on February 1,2010 | 04:14 PM

    This is probably a stupid comment, but, as I understand this story, the doctor took cells from her 'cancer'. He took cells from the tumor. I would like to know wouldn't that change the whole dynamics of their research, and perhaps even explain why they never died?

    Posted by Judy Dale on February 1,2010 | 04:14 PM

    Rebecca, you should be very proud of your self. You have not only created an interest in Henretta Lack but you also created interest in cell research. You have gotten people stirred up about something important. That is what writing is all about and you've done it my dear. Kuddos to you for starting a buzz that won't die any time soon. Good luck with your book and in your life. I do hope to hear more about you in the future. I'm sure there are many good things in store for you and yours. God Bless!!

    Posted by Rhonda Hall on February 1,2010 | 04:14 PM

    So many comments here are SO self-centered!!! Nobody MADE "millions of dollars" from these cells! Were some sold - yeah, and most of that $ went to paying for keeping the cell line going and available for further studies. Most were just shared from lab to lab. I GUARANTEE the scientist who cultured the cells first didn't make squat from it. So there's no huge pot of money to hand out to her family. There's nothing terribly unique about these cells - they just happened to be the first cervical cancer cell line prepared, so got spread around to labs first. There's a bunch of other immortal cervical cell lines out there just as good - nothing really unique about this one. And NO - it CAN'T get spread around by dust!!! - just by sloppy cell culture techniques. And yes, I DO work in the field and know what I'm talking about. There was nothing unique about this patient's cells - they were just the first cultured. Why does everyone want and expect money for doing nothing??!??

    Posted by Tom M on February 1,2010 | 04:14 PM

    yeah the cell aren't immortal they just outlived her and will die...so their intent on using the cells is great but what happens when they eventualy die and there or more diseases P.S im 11 years old =)

    Posted by Chanel on February 1,2010 | 04:14 PM

    Wow this sounds VERY interesting.I would love to know what happened to Henrietta's family and if they ever were compensated.

    Posted by Talk of NJ on February 1,2010 | 04:15 PM

    I am pleased to read about this, HeLa cells have helped many people today as well as will help many others down the road. Think about all the ones with cancer our kids husbands wife's grandkids and so on. If it was not for her cells we would not have what all we have today think about that when you get medical treatment or your loved ones. If I had this type of cell that can go on and on I would be happy to know that my cells were living on past me helping others even if I died from something. To seek money for this is wrong who knows for a fact she didn't want her cells taken or that she would not want this to be done to help others read the story again and what it has helped go read the book and learn before you post things that you know nothing about. I hope one day cancer and aids is done away with and it comes out that this was from HeLa cells that helped them find this cure but as we all know the American way is to sue and get money as long as we can get rich too who cares about the good that comes of it as long as the I get rich too plays in that is ever so sad and we as Americans need to stop this and look at the good we can do for others.

    Posted by Scott on February 1,2010 | 04:15 PM

    I only hope and pray that the family gets financially rewarded for their unwitting participation in modern medicine. Please keep the world informed of the efforts of the family in this regard.

    Posted by Jason D. Rahming on February 1,2010 | 04:15 PM

    What a great story. I had never heard of the HeLa cells until now. Maybe she was a super hero...haha. How shameful that her survivors are now speaking of money...dummies

    Posted by Lori on February 1,2010 | 04:15 PM

    wow thanks so much for this interview! it really makes me interested in science probably because it has a human element. great work and can't wait to read the book!

    Posted by elena finley on February 1,2010 | 04:15 PM

    That story is amazing. So black people do make positive contributions to science after all! We continue to do so, but nothing is ever written about us, until someone unearth the truth. The family should have been notified, and compensated. This is just one of those injustices that black people have to endure right? Thanks to the author for unearthing the truth and being bold enough to tell the story! God is in control, and He will allow more pertinent information to surface about blacks and other minorities which will show the world that we are people also, and that we are just as important to the planet!

    Posted by Christine on February 1,2010 | 04:15 PM

    My Condolances go out to Henrietta Lacks whos cells were important for making it possible to help with the polio vaccine possible.

    Posted by George S. Hansen on February 1,2010 | 04:15 PM

    thought this artical was very interesting and yes, i will read the book when it's out. good job

    Posted by joseph on February 1,2010 | 04:16 PM

    I think this was certainly a fascinating piece of work, however this family definitely deserves to be compensated. Who's to say how many millions of dollars were made by the research community in their various studies of the HeLa Cells. And to the response that in the 50's they didn't have to let her know that her cells were being taken for research purposes, you say none of what was done was illegal back then.....one better...just about everthing done in terms of blacks and whites was illegal back then. Imagine what would happen in today's society if that were done. There would be a lawsuit before the operating room got cold. It's unfortunate to think that someone might have taken her cells in the name of treatment and then possibly failed to treat her. Does anyone have this information? I can't help but think of the story of Mrs. Ever's Boys.

    Posted by DG Sam on February 1,2010 | 04:16 PM

    Thanks for sharing this beautiful story. I agree with Sandra H. Also, I think if only Henrietta (R.I.P)can speak now, she would want her children to be taken care of. The family should get the "Royalty Fee".

    Posted by may on February 1,2010 | 04:16 PM

    Quick! Send your DNA sequence into the the patent and copyright office! That's the only way you can protect yourself in our soon to be "Brave New World" Your doctor could find the cure for the common cold hidden in your genetics and he'd get the Noble Prize, you'd get nothing except his bill.

    Posted by taxpayer576 on February 1,2010 | 04:16 PM

    There is nothing special. The cells just outlived her. Everything has a start pick and finally the death. We just dont know the time of death.

    Posted by Ref on February 1,2010 | 04:16 PM

    Interesting article! I assume scientists have investigated if it is CANCER cells which are immortal? That would explain why cancer is so hard to cure!

    Posted by Laura on February 1,2010 | 04:16 PM

    That had to be one of the most interesting pieces I have read in a long time. I actually read the whole thing. When does the movie come out?

    Posted by Susie B. on February 1,2010 | 04:16 PM

    As many blacks as possible should get together to sue Johns Hopkins Hospital in Baltimore, Maryland for taking this black womens cell samples with out her permission and spawning new medical and financial developements without making her family aware of what they have done without her permission. If the tables were turned they would not hesitate to take action against a violation of doctor and patient trust.

    Posted by Lieberman on February 1,2010 | 04:17 PM

    Reminds me of the Tuskegee Experiment, in which Black men were denied treatment for syphillis and suffered horribly as doctors watched and studied them. In the racist America of the 1930's. There was a movie , Mrs. Eversboys. The men went blind, insane and were in great pain for years as the white gov't doctors watched and observed them (like animal testing) The family MUST be compensated ASAP. it is like involuntary organ donor.

    Posted by amina on February 1,2010 | 04:17 PM

    i feel so sad with the family knowing that they could have live in a better way but it's not too late i hope they get whatever they're entittled to.thank you

    Posted by marjorie on February 1,2010 | 04:17 PM

    Great story i would love to learn more about this story .

    Posted by vfox on February 1,2010 | 04:17 PM

    Gee, sure sounds like an engaging story....too bad the power behind its impending fame comes from its warm and fuzzy feeling and not from truth. In my honest opinion there is absolutely no way of nearly 99 percent of the readers to ever know if the story is really true or not. But that doesn't really matter, because most will believe that it is, and the need to acknowledge the true source for some "mysterious" never dying cells will be forgotten and soon pass into unknown history.

    Posted by Kevin on February 1,2010 | 04:17 PM

    The book is "The Immortal Life of Henrietta Lacks" by Rebbeca Skloot. An Internet search will lead you to where you can purchase the book. It will also tell you about the author and other books/articles she has written. Remember -as long as we remember Ms. Henrietta, she is alive. Therefore, if science can keep her cells alive, we can do our part by keeping her memory alive as well.

    Posted by Ruben on February 1,2010 | 04:18 PM

    I agree this is a very interesting and amazing story, but will someone please explain why anybody owes the family any money? It is standard procedure for a doctor to take cells and have them tested every time a growth, tumor, mole, skin scraping, etc. is removed when trying to determine a diagnosis for a problem. It's another method to confirm or deny a cancer (or other) diagnosis. And the doctor does not pay the patient for the cells that are taken for testing. As I understand the article, the cells were taken from the tumor while she was alive. The cells were shared because they were "special" and didn't die. Naturally the doctors were interested in finding out why they didn't repsond as most other cells did. So, why does anybody owe the family "a lot of money?"

    Posted by MaconBookkeeper on February 1,2010 | 04:18 PM

    Very interesting BUT Can the cells multiply and can they survive the strane of virus' - is that what is meant by "immortal"

    Posted by Warren on February 1,2010 | 04:18 PM

    The gov has everyones dna (cells) on file, make no mistake. When a child is born the first thing they do is the PKU and send blood samples in. They get tested for genetic disease and such and cataloged. Do we get a check in the mail when our children's blood sample proves useful? Nope. 50 years ago they had no idea what her sample, really any sample, can do for us today. She will be forever knows as the immortal woman and save millions of lives. Who else can say that?

    Posted by Angi on February 1,2010 | 04:18 PM

    Why shouldnt her family want compensation? If she were white you better believe they would want compensation too. These comments about money are ridiculous. As if no money was made off of the vaccines that resulted from her cells. This was done without her knowledge and it follows a long history of doctors taking liberties with black patients, regardless of whether it was "legal" at the time. Read the book "Medical Apartheid".

    Posted by Gina on February 1,2010 | 04:18 PM

    Really cool!! Thanks lovely lady.

    Posted by Eddie on February 1,2010 | 04:19 PM

    What on earth did her family do to deserve a single dollar? One laughable comment observed that taking those cells without her permission was 'malicious.' Hey you little know-nothing, when polio vaccine became available in the 1950's my mother cried in relief, for many children in our town and hundreds of other towns were already suffering from what was a cruel and lifelong affliction.

    Posted by Bill Parker on February 1,2010 | 04:19 PM

    Thanks so much to the person who took interest in a young black woman’s (Henrietta Lacks) story. Not to sound racist, but so often blacks are pushed aside and never honored for the advancements made in this country. Usually, we only hear about how a white person created this or helped invent that, but very seldom do we look at what contribution and impacts the black community has made to society; other than Martin Luther King, Malcolm X, Zora Neal Hurston and a few others (not many). This was a nice tribute to the Lacks' family. Now can someone help these poor people get some type of restitution for all that has been done in secrecy? This great woman has paved the way for so many scientific breakthroughs, such as developing polo vaccines, scientific land markings, gene mapping and the biggest one of all in vitro fertilization. Just read the article yourself, it’s all there. Indeed, the right thing to do for the scientific world would be to offer the family some type of compensation.

    Posted by shontovey on February 1,2010 | 04:20 PM

    Nice information...perhaps another step towards opening the human related knowledge.

    Posted by Shoukat Ashraf on February 1,2010 | 04:20 PM

    WOW -Just more reinforcements that black people have been apart of and instrumental in all phases of american history since they arrived on the slave ships. We have seen our first black president - will we ever see white people salute us as a race and thank us for all of the inventions and history making events we were apart of - I only hope in my life time.

    Posted by Hattie on February 1,2010 | 04:20 PM

    This was a fascinating article! What was most intriguing to me was the unexpected "immortality" of the HeLa cells. It brings questions to mind such as: Does man have an inherent desire to live forever? Why do we die? What hope do we have for the future? This article reinforces that our bodies, with the promises in the bible, do have the potential to live forever, in a paradise Earth.

    Posted by Angie on February 1,2010 | 04:20 PM

    Wow , this is a true piece of work, congratulations , guess i'll buy the book.

    Posted by Ray Lopez on February 1,2010 | 04:20 PM

    What happened with Henrietta Lacks and her HeLa cells is a good example of the indifference that the American Medical stablishment have when it comes to research on minorities. I think that because this case of HELa cell was extremely profitable, it was so easy to compensate Mrs. Lacks's family with a few millions giving to Mrs. Lacks new generations of grand and great grandchildren, the opportunity to go to school and, perhaps, get into the medical field to continue the heritage of Mrs. Lacks who without knowing it contribuite enourmously to science. I wonder if instead Mrs. Henrietta Lacks those cells and tissues were belonging to Mrs. Reagan, Mrs. Rockefeller, or even Ms. Middle Class White Lady ( any prominent last name you choose to fill the example). It is so sad the world of competition and greediness in America that , so far, still corroing the ideals of developing life with human dignity and freedom for " We the People". Respectfully, Marlen Arguedas-

    Posted by Marlen Arguedas on February 1,2010 | 04:20 PM

    INCREDIBLE!! It's amazing to realize the way our human cells are created to live on and be of use to humanity either through research or providing services to individuals even after we decease. I agree that the medical professionals should take heed to this story and be aware that each human life is precious and life should never be exploited, even in the name of medical research and it's recent advances. It's apaling to hear that a poor black family not benefitted from their mother's own legacy in the cell research department. I hope retribution has been made since then and the Lacks family has been able to profit and live better lives.

    Posted by Bernadine Wolford on February 1,2010 | 04:21 PM

    It is a very fresh look at the contribution to science made by a young black woman. Given the history, Being a farmer, she was not well-educated. So, she signed a release form she didn't understand. Since we're told a "piece of the tumor was taken without her permission" she probably only signed a surgery release form. I'm very intrigued & would love to read the book. I suspect its release will result in Henrietta finally being credited for her part(unknowingly)in medical breakthroughs realized by the use of her cells - finally.

    Posted by Pamela on February 1,2010 | 04:21 PM

    I think the story about HeLa is amazing,I am thinking of leaving my remains to the medical university in Mi. I never had any childhood deseases that most children get and until I was 55 did I was in good health. Now ever thing is hitting me, diabeates,high blood pressure,obease,can't walk 100 ft. without getting out of breath. just turned 75, had a good life,so as a last act maybe science or medical can find use in what is left. Take any organ you can use even the brain and cremation at the end. thank you GB

    Posted by girard bilazzo on February 1,2010 | 04:21 PM

    The book is terrific - I read an advance copy. And Rebecca has set up a website AND a foundation for the family http://www.lacksfamily.com/

    Posted by Julie on February 1,2010 | 04:21 PM

    <<< What a great contribution to mankind H. Lacks made whether she knew it or not. If I could help in such a way I would do it freely and without any thought of monetary compensation so long as it goes to a true, non-profit entity (if there are any.) Back in her day informed consent or permission was nonexistent - thankfully we have it now and just hope it can be taken to the next level. Today money greedy companies, not the humanitarian minded, are behind many of these activities. I believe informed consent needs to include a statement regarding the actual profiteering from such activities so that the individual can decide to assist freely or join in with the money greedy companies to attempt to profit from it. >>> ###

    Posted by Mike Ortin on February 1,2010 | 04:21 PM

    Can cells like that be used for a cure for Huntington's Disease? HD is an incurable disease. PLEASE PLEASE we need a cure.

    Posted by C. Pope on February 1,2010 | 04:21 PM

    Well that is good in a way...but in another I smell hidden agenda...then again nothing in this world surprises me anymore.

    Posted by Lola19 on February 1,2010 | 04:22 PM

    People "GIVE" their bodies to science all of the time in an effort to help someone else. Why do people always feel they must be compensated? Some people are so greedy.

    Posted by KLR on February 1,2010 | 04:22 PM

    Wonderful story. I will read the book. Very interesting. Isn't it possible to perpetuate a cell indefinitely if it is cultured on a regular basis? It seems to me that this sort of thing is done in labs when it is essential to keep a certain strain viable. I know it is possible to purchase cultures and use them experimentally. Maybe human cells are different, but I don't think so

    Posted by nick mihalopoulos on February 1,2010 | 04:22 PM

    What an amazing story and equally amazing is the research behind it. What is also interesting is the fact that the researcher's teacher just happened to know the first name of the patience from which the cell sample was taken. The teacher also happened to know that this patience was a black woman while it appears others were trying to conceal this lady identification. It gets even more interesting to hear about how the researcher was facinated with the few facts she heard from her teacher at an early age and never forgot this and would never rest until she could find out the facts surrounding this mysterious contributor to medical science. Again a fascinating story in which we all will be better off knowing more about these incredible events behind the story. I say to the reseacher, "you were chosen to tell this story to the world."

    Posted by Tony Hall on February 1,2010 | 04:23 PM

    it's just so easy for someone to say - henrietta's family should have been compensated MILLIONS..uhh, BILLIONS!!! it's like saying- my pimple had sometning to do with the success of an anti-acne medications. HeLa cells were apparently given to another person without her consent. now that's a legal issue. not a monetary issue. that's why we frown on "selling your kidney". god should be ccompensated if it worked on the recipient. you sould be compensated if you "invented" or "created" something. atheist cannot be compensated for their body part because they are here "by chance" or cosmic accident.

    Posted by FILMORE RIEGO on February 1,2010 | 04:23 PM

    With those cells... I could begin my WORLD TAKEOVER. I'd make my own personal Lazarus pool... No, just kidding. On a serious note, this must raise a lot of suspicion regarding medical and other practices prior to standardization during the laissez faire period. Begs the question of how many more stories like this exist and have yet to be uncovered.

    Posted by Victor on February 1,2010 | 04:23 PM

    These were cells from a TUMOR, the tumor was destroyed. The family deserves NO compensation. The thinking/lucky Doctors & scientists who used these tumor cells are to be commended. I am greatful that THEY were forsighted enough to scavange these cells. I am very sorry that this woman died, and from such a terrible disese but because of her so many were helped. My mother back in the 1960's was used as a guinea pig for cancer research. I nor any member of my family want any money, and never have. Did she help the world - YES! Was the treatment effective - no, unfortunately. Would we, her family, allow the Doctors/scientists to do this again - YES, it just might save someone else's mother.

    Posted by Joyce on February 1,2010 | 04:23 PM

    Does it bother anyone else that they took the sample without her permission and then tricked her family into becoming guinea pigs without ever compensating them. I feel sorry for the millions of Americans without health insurance that undergo unnecessary tests because they can't pay their hospital bills. What's an anti-depressant?

    Posted by Ashley Brook Smith on February 1,2010 | 04:23 PM

    The mere fact that secrecy was involved would make one wonder. The scientist knew exactly what he was doing and knew that he could get away with it, because others before him have done the same thing and have prospered. (There were always excuses when found out.) Millions have been helped, help this family.

    Posted by Jennye Grundy on February 1,2010 | 04:23 PM

    I wonder if there is a possibility that the cells weren't hers afterall and that they were some of the one's created by scientists?

    Posted by Arlen on February 1,2010 | 04:23 PM

    I actually heard the story about Mrs. Lacks many years ago and like T. Diamond, I thought it would make a great documentary film. I actually found it distrubing and disagree with the author. To me the use of someone's essence without consent, regardless of leading to some great gains in the science/health field, is ghoulish. Forget the billion dollar industry it has spurned, it is like stealing part of her soul over and over again. Sugarcoat it however you wish, but it is clearly another example of the poor and uneducated being taken advantage of and blantanly deceived.

    Posted by Jonathan D. on February 1,2010 | 04:23 PM

    Cool story. I worked 12 years as a Molecular Biology researcher and worked directly with Hela cells and tissue culture. Thank you so much for stating the importance of these cells in research. We could do so many important experiments and find very important things out about the Molecular Biology of cells, their structure, and ways to help cure diseases. This has helped so many lives in so many ways, it is literally unimagineable. Unfortunately, federal law now states that a person does not have ownership of discarded material from their body, so it is not likely that the family will see any money from this. Maybe knowing how much it has helped human lives might be enough for them. There certainly is an ethical question here about how far is too far on the use of these cells. It would be strange that's for sure!

    Posted by Jo Pen on February 1,2010 | 04:24 PM

    This story would be a great movie combining the story of writer's research and the daughter coming to terms with her mother's historical significance, the brother's monetary interest and the father's lack of understanding the situation. And remember several years ago when a company was selling parts of bodies donated to science. This stuff happens.

    Posted by Suzanne on February 1,2010 | 04:24 PM

    What a lovely couple peers from the photo! Looking at her fur shrug and hat and his pressed suit, the two must have been celebrating something. As a share cropper's wife in tobacco country, Henrietta could not have known how she may have saved her children and grand-children from polio. To think that she would unwittingly pave the escape from suffering (polio) for so many children and parents, not to mention all of the other medical progress made with a small piece of the body that failed her. Amazing. Her family deserves every blessing coming to them.

    Posted by Mary on February 1,2010 | 04:24 PM

    Darna Young you expressed my sentiments exactly. Since her cells never died according to this author, I doubt if they even tried to treat her. That call to the home should have been followed up with a visit to explain what was going on. For the benefit of science, they should have explained it to the husband in a way he could understand what was going on with his wife. While I agree that the sons are greedy, I do believe that Deborah should receive compensation for she is in it from the heart. This is her mother she is deprived of all these years and for to be minimized by some responding as just a cell on a petrie dish is disrepectful and harsh. The history of blacks and medical science has always been questionable--remember the young men given syphillis. It's one thing to donate your body to science and quite another to have it stolen from you.

    Posted by Dai on February 1,2010 | 04:24 PM

    I AGREE THE FAMILY SHOULD GET SOMETHING FOR ALL THAT HAS BEEN DONE TO HELP OTHER PEOPLE... BUT REMEMBER BACK IN THE 50's PEOPLE DIDN'T THINK OF IT THAT WAY, ALL THEY THOUGHT ABOUT WAS THE SCIENTIFIC VALUE. THEY WANTED THIS TO WORK TO HELP OTHERS... WHY IS IT YOU PEOPLE ONLY THINK OF IS "MONEY". MONEY IS THE ROOT OF ALL EVIL, AND NO I DO NOT HAVE MONEY I'M 73, AND LIVING ON SOCIAL SECURITY...

    Posted by MARIE on February 1,2010 | 04:24 PM

    I think this is the most interesting thing I have ever read. Wow though it is scary knowing that someones cells floating around in the air can contaminate. But I am going to school to be a nurse and I would love to learn more about things like this.Guess I will have to invest in the book too. But I think the family deserves some of the money because they have been living in poverty for so long and it WAS their mother, and the scientists did take it without permission. So somebody is entitled to something here. If it was me I would be fighting too for what is rightfully mine. I wouldnt want it all just compensation.

    Posted by Misty on February 1,2010 | 04:24 PM

    Very interesting story!!!

    Posted by Maricar on February 1,2010 | 04:24 PM

    Why would the family be entitled to ANY money? They didn't do anything to earn the money. Doesn't earning money require the family do something to earn it? I think there are too many people who think the world owes them something for doing nothing... I think this is a great story. Think of how much good science came from these experiments!

    Posted by Henry on February 1,2010 | 04:24 PM

    This precious lady deserves the thanks of all of us. That being said, how does her great gift to mankind translate into payments to her present day relatives? Sounds like the the same old story. Greed among the surviving family menbers. Remember the MLK family squabbles? How about all the fighting surrounding Michael Jackson's clan? Greed, Greed!

    Posted by danman on February 1,2010 | 04:25 PM

    I find it fascinating that so many posts are about monetary compensation here. So much for people trying to better the human race these days i guess unless payment is involved

    Posted by Kent on February 1,2010 | 04:25 PM

    Great story. where can i buy the book. The the lacks family deserve their fair share.

    Posted by Ed Origenes on February 1,2010 | 04:25 PM

    I'm a little appauled that there arn't more comments. This is an amazing story telling a great deal about how we've grown as a culture and even a little about what we can expect from our sientists in the future! I fully agree with the comment that this should be turned into a tv documentary. I'm glad there's a book out, but tv would bring it to that many more people. Peolpe need to know!

    Posted by Shi on February 1,2010 | 04:26 PM

    Was it merely serendipity? Or is there anything really remarkable, scientifically speaking, about these HeLa cells? You say the cells never died. Do you mean individually? Or do you mean that scientist have continuously grown them in cultures? The former is immortality, in a sense, and quite remarkable. The latter is typical journalistic spin.

    Posted by R. Hill on February 1,2010 | 04:26 PM

    This was a very interesting read from the moment i saw it I had to find out more, truly amazing. I look forward to reading the book.

    Posted by Josephine on February 1,2010 | 04:26 PM

    The multi-million drug industry needs to pay these people.

    Posted by pam Storey on February 1,2010 | 04:26 PM

    I just read that the family got NOTHING. Which is terrible. They should have received something being that the doctor didn't ask permission. Her cells have saved how many lives? I'm not saying give them billions but they should each be living comfortably.

    Posted by Ash on February 1,2010 | 04:26 PM

    I actually heard the story about Mrs. Lacks many years ago and like T. Diamond, I thought it would make a great documentary film. I actually found it disturbing and disagree with the author. To me the use of someone's essence without consent, regardless of leading to some great gains in the science/health field, is ghoulish. Forget the billion dollar industry it has spurned, it is like stealing part of her soul over and over again. Sugarcoat it however you wish, but it is clearly another example of the poor and uneducated being taken advantage of and blantanly deceived.

    Posted by on February 1,2010 | 04:27 PM

    That was a wonderful piece! I realy enjoyed reading it as well. I appalude you for your persistance with Mrs. Lacks family. Had you not, her daughter would still in wonder of her mother. You were able to give her a piece of something she "never" had, Her Mother! As for the finacial matter of the whole situation, that as well would still be a dark spot in their lives. I pray everything was worked out in a reasonable matter. Again, I comend you on a wonderful piece.

    Posted by L A Stokes Dallas, Tx. on February 1,2010 | 04:27 PM

    This is a very compelling story. I don't know how the family could equably compensated since this cell line has made researchers millions. Family members not compensated initially will start coming out of the wood work. However, it is displeasing to me that the immediate family of a cell line that helped cure polio should be homeless and without health benefits. Go figure!!!

    Posted by Micheal on February 1,2010 | 04:27 PM

    I agree that the family deserves compensation,also, is the author who will profit from this book giving them any royalties?

    Posted by David on February 1,2010 | 04:27 PM

    I had two female cousins who were among the ones experimented on in Tuskegee Alabama. They were told that they were going to be cured for syphilis, but we learned later when the story was told that they had been used to experimental purposes.

    Posted by Marjorie Pettway-Harlin on February 1,2010 | 04:27 PM

    Wow thank you so much for your obsession with this story! Can't wait to read the book!

    Posted by Sari on February 1,2010 | 04:28 PM

    I retract the 'not enough comments' statment. my comp glitched. I still stand by the rest of the statement, though.

    Posted by shi on February 1,2010 | 04:28 PM

    I find this very interesting , thank you for sharing. Would love to learn more about Henrietta Lacks and what was found out about the rest of the familys cells.

    Posted by Maryann Oliveros on February 1,2010 | 04:28 PM

    even though they are not "immortal" they are a nice thing to have!

    Posted by Bob on February 1,2010 | 04:28 PM

    what was done to her even though it was the wrong way has open doors for scientist to explore ways to continue to help in the medical industry.we must buy the book to learn moer about this great black pioneer, if i can call her that. A remarkable story that we as a black people and people in general must treasure. someone said that money was not owed to the family but i disagree,even though she signed paper if she indeed did,her family deserves compensation because we are talking about something that happened in 1950 and thereafter.I could not stop reading this article because i believe that this is PURE HISTORY.

    Posted by kat on February 1,2010 | 04:28 PM

    Very Interesting,want to learn more,need info on the book. Would LOVE to read.

    Posted by madelyn J. on February 1,2010 | 04:28 PM

    I think it is such a travesty that these "so-called" scientists extracted this woman's tissue for experimental research without gaining the permission of this beautiful woman's family and probably without the least bit of actual treatment for the cancer from which she suffered, nor compensation to the family. I, for one, will not find this book an interesting read, and will not read it, as it only confirms how the "haves" of this country have taken advantage of the "have nots" and it still continues to this day. This family is owed a GREAT DEAL OF MONEY for the use of their family member's cell tissue in landmark scientific studies!

    Posted by Shay on February 1,2010 | 04:29 PM

    I think it is such a travesty that these "so-called" scientists extracted this woman's tissue for experimental research without gaining the permission of this beautiful woman's family and probably without the least bit of actual treatment for the cancer from which she suffered, nor compensation to the family. I, for one, will not find this book an interesting read, and will not read it, as it only confirms how the "haves" of this country have taken advantage of the "have nots" and it still continues to this day. This family is owed a GREAT DEAL OF MONEY for the use of their family member's cell tissue in landmark scientific studies!

    Posted by Shay on February 1,2010 | 04:29 PM

    What an amazing piece of history and science! What a way to begin BLACK HISTORY MONTH! Please find a proper way to honor the(HELA)family. I am sharing this piece of amazing history and science with the science teachers that I know.

    Posted by Joyce on February 1,2010 | 04:29 PM

    This family is owed money.

    Posted by zenepher on February 1,2010 | 04:29 PM

    THIS IS ALL VERY INTERESTING. HOWEVER IF SCIENTISTS ARE GOING TO BE USING A HUMAN BEING AFTER DEATH FOR EXPERIMENTS, MOST DEFENITE THE FAMILY SHOULD KNOW, AND EVEN HAVE THEIR PERMISSION TO DO SO. WHO KNOWS MAYBE THEY CLONE PEOPLE AND WE DONT EVEN KNOW. IMAGINE SEEING SOMEONE IN THE STREETS THAT LOOKS LIKE A DEAD RELATIVE, AND YOU THINK IS JUST A LOOK A LIKE AND THEY ARE ACTUALLY YOUR FAMILY. ALL VERY CONTROVERCIAL !

    Posted by ALINA on February 1,2010 | 04:29 PM

    I find it interesting to see how many people think that there should be some compensation to the family. The family did absolutely nothing towards the research that was done with these cells. This type of research is done every day. There are people donating their bodies to science after death every day. Without this process, we would never have any cures for anything. Even today, if you have any type of surgery, biopsies are taken and cultured. You do not get paid for it, you have to pay for the service.

    Posted by Ken on February 1,2010 | 04:29 PM

    Very interesting article indeed. I am most interest in reading the book. Pitty though, the family should have been compensated as HeLa cells are the foundation of many scientific research.

    Posted by Shan S on February 1,2010 | 04:29 PM

    So, are you giving a cut of your book sale profits to the family?

    Posted by Weasel on February 1,2010 | 04:29 PM

    Often science is thought to be done in a vacuum, but actuality reminds us that humans are always in the equation. As someone trained in the sciences and a member of the human race, i would suggest that we remember that times and society change. That although our own personal objections are a reflection of our current experience...the 1950's was a whole other ball of wax of science and society. This isn't an excuse for bad ethics but all things in the past must be looked at through proper lenses. Do i agree that the patient and family should have had rights of knowledge? sure. Does that mean that things would be different because of it...not necessarily. The science aspect of the story is awesome, the gift of knowledge however obtained is priceless. Like all great stories, the good and the bad have their parts to play.

    Posted by Shannon on February 1,2010 | 04:29 PM

    Really nice story, but at the same time I can't help feel a little privacy invasion with the extraction of the cells. Is the approval of the patient required?

    Posted by Bernadette on February 1,2010 | 04:30 PM

    God bless this family and if they haven't been richly compensated they should be....and soon.

    Posted by Ann Richey Smith on February 1,2010 | 04:30 PM

    Great story - hopefully the family can also benefit as society has.

    Posted by RM on February 1,2010 | 04:30 PM

    Love the story behind this and think it's interesting to have a story behind a cell sample that changed the world but as for paying the family restitution? How many other families would have to be compensated for cells that contributed to science and healing? I for one would glady donate cells if I knew there was even a chance it could save a life someday! Really...for free!

    Posted by Karen on February 1,2010 | 04:30 PM

    This is amazing story ingeniously written. Good work!!!!

    Posted by Adeniyi Adeboye on February 1,2010 | 04:30 PM

    Fascinating and unfortunate. Thank God, that cell-research have some guidelines in this day and age.

    Posted by gmurphy on February 1,2010 | 04:30 PM

    The Lack's are a most handsome couple and dressed exquisitely. Not all farmer's were poor. Many considered themselves as "country gentlemen" farmers. Nevertheless, they will be remembered for Henrietta's contribution to science.

    Posted by richard on February 1,2010 | 04:31 PM

    this isint about black and white ppl,its about trying to understand the cells and try to make something of it like a cure for a disese or something. (Sorry about bad spelling)

    Posted by Marc on February 1,2010 | 04:31 PM

    I believe if the doctors took a sample of the tissue and anybody that profited from the taken of the tissue should be reponsible for any monies. Yes, I think the family members should be entitled to any and all money. However, who knows with the way government and other organizations work with each other to shelter them from paying. So sad.

    Posted by sean on February 1,2010 | 04:31 PM

    TUSKEGEE ALL OVER AGAIN

    Posted by Morgan Coleman on February 1,2010 | 04:31 PM

    Is this a fiction?

    Posted by yahaya on February 1,2010 | 04:31 PM

    What is wrong with you people? So the concensus opinion here is that giving up a few cells should "cost someone some money". Shame on you all! Is it realy like this unknowing cell donor should win the lotto... perhaps this "ambulance chacing" attitude is a BIG part of our health care problems. Everyone feels entitled to get rich over something that really has had no negative effect on them. Perhaps some of you need a reality check - how does science advance cures without cells?

    Posted by Mike on February 1,2010 | 04:31 PM

    I found this: Hela cell is an immortal cell line used in medical research. The cell line was derived from cervical cancer cells taken from Henrietta Lacks, who died from her cancer in 1951. The cells were propagated by George Otto Gey without Lacks' knowledge or permission and later commercialized, although never patented in their original form. There was then, as now, no requirement to inform a patient, or their relatives, about such matters because discarded material, or material obtained during surgery, diagnosis or therapy was the property of the physician and/or medical institution. This issue and Ms. Lacks' situation was brought up in the Supreme Court of California case of John Moore v. the Regents of the University of California. The court ruled that a person's discarded tissue and cells are not their property and can be commercialized.

    Posted by Michelle on February 1,2010 | 04:31 PM

    so interesting and amazing story.. hope the family could get benefit from it............

    Posted by cecille carillo on February 1,2010 | 04:31 PM

    wow! very interesting indeed, however, i feel because mr. lacks had a 3rd grade education and did not understand what was being done in research and science with hela cells. he and his family was being taken avantage of for over the twenty - thirty years her cells were being used and should be compensated for it!

    Posted by bobbie on February 1,2010 | 04:31 PM

    very interesting. thank you

    Posted by carolina on February 1,2010 | 04:32 PM

    The time frame of when it happened is of little consequence, but knowing how our country has treated other cultures over the many years of its history is both appalling and upsetting. The family should be compensated, but it may be unlikely to happen unless there is a public outcry for it to happen. Little is done unless what was done in the dark comes to the light and people react to it negatively, so the government would need the public to act crazy to get the due compensation for this family. The story is very good and I will be getting the book. It is doubtful that it will be required reading in our general public education system and if it ever does come out the focus will be more on the scientist than the donor because of the work that they put in. We must educate our own children and not leave it up to others. Thanks to the author of the book and the family for caring enough to let us know... Blacks matter in the USA...

    Posted by Kim Lambert on February 1,2010 | 04:32 PM

    Just to clarify, many cancer cells taken from individuals are immortal and used in biological research - as is noted, tissue culture has played an major role in scientific breakthroughs over the last 50 years. In addition, use of human cells in tissue culture for experimental studies can in some cases substitute for experiments which would otherwise need to be done in laboratory animals. For those who are interested, there is a California Supreme Court case Moore v. Regents in the 1980s which addressed the issue of whether biological material taken from a patient without the patient's consent can be used for commercial gain.

    Posted by Tom on February 1,2010 | 04:32 PM

    Something about this story just screams HIPPA violation. I also doubt that anyone's cells taken today would ever be identified 50 years down the road. Our society has become paralyzed with fear and we place way too much emphasis on privacy over the pursuit of scientific/medical innovation. While I believe that the basic protection of personal information is imperative, there needs to be a balanced understanding of what deserves (or needs) protecting. Interesting story, though...i look forward to learning more about it all.

    Posted by Bob on February 1,2010 | 04:32 PM

    What is this book called? cuz' i want to read now :P is it called "henrietta lacks immortal cells?"

    Posted by tina on February 1,2010 | 04:32 PM

    You had me until the race card was played... I was waiting, I knew it is coming.... sad!

    Posted by bootzy on February 1,2010 | 04:32 PM

    Awesome story!!! Very nicely written. I agree that this is something that should be included in school curriculums. This makes science and research very interesting - you want to learn more. Thanks for your tenacity in bringing life to this story.

    Posted by Oretta on February 1,2010 | 04:32 PM

    Vow! This is a must read!

    Posted by JJ on February 1,2010 | 04:32 PM

    If she was 30 in 1951, she would have been 89 today. Her cells should have lived that long anyway. The fact that they have been so useful in research is attributable to good science, not immortality on the part of the (unsuspecting)donor.

    Posted by Mel Walker on February 1,2010 | 04:33 PM

    Even though all things live and die this goes to show that something in Henrietta's cell allowed an infected or diseased cell to live when they are expected to die. This is vital to research. With the HeLa cells researches can try and find an explaination as to why her cells lived for so long when infected. With this information people who are infected may have a longer life span and who knows maybe give them time for a cure or vaccine to be found.. Love the article by the way. Its eye catching and I'm more interested in the after math of everything.

    Posted by Ariel Garcia on February 1,2010 | 04:33 PM

    pretty sad that those poor people were lied to for so many years. Not sure if there were such things as HIPPA laws back then. Other than that, A great story!

    Posted by Deanna on February 1,2010 | 04:33 PM

    What amazing story. I what to know more

    Posted by Pat on February 1,2010 | 04:33 PM

    AMAZING!!!

    Posted by KAREN BROWN on February 1,2010 | 04:33 PM

    Well done, I actually want to read the book now. One day we will use cell research to cure even death. The world can be a beautiful place!

    Posted by Max on February 1,2010 | 04:33 PM

    The key phrase in this piece was 'took a piece of the tumor without telling her'! Considering her race and the time in history when this occurred, that phrase opens the door for MANY questions. This article was interesting and VERY troubling. Did they even attempt to treat her in any way and assuage her pain or did they just steal her cells???? I want to know those answers!!!

    Posted by Debra on February 1,2010 | 04:34 PM

    I read this book in manuscript form and was completely blown away. It's remarkable in several ways, but its most outstanding feature is its ability to capture you - no matter how clumsy your grasp of science (and mine is plenty clumsy)- in its spell-binding thrall. I've been describing it to friends as a "blood-cellular thriller." I can't recommend this book highly enough.

    Posted by amanda on February 1,2010 | 04:34 PM

    Fascinating story.. Can't wait to read the book. This is one I will read with my daughter. Thank you Henrietta!!

    Posted by Crystal on February 1,2010 | 04:34 PM

    I to found this piece of history to be a great breakthough for science, but I' am also sadden that no one had check with the family to get approval. I wonder if her family would be willing to go to court.

    Posted by april on February 1,2010 | 04:34 PM

    I guess all of us who didn't get polio could send the family a dollar (each). Wouldn't that be an ideal way to address the issue? I know two women in their 40s who had polio, and everytime I think of either of them I am grateful my vaccine was effective. Then again, is the daughter a collaborator on the book, and does buying it give her anything?

    Posted by toriadori on February 1,2010 | 04:34 PM

    This is an amazing story, ingeniuosly written!!! Good work

    Posted by adeniyi adeboye on February 1,2010 | 04:34 PM

    what a bunch of crap you dont know if she gave her permission or not , you are just assuming.

    Posted by ray on February 1,2010 | 04:34 PM

    Very very nice!

    Posted by T on February 1,2010 | 04:34 PM

    I FEEL THAT NOW,MORE THAN EVER BEFORE WE SHOULD BE HONEST. AND TELL THE TRUTH ABOUT THE HISTORIES OF OUR LIVES. THIS LADY, MRS HENRIETTA LACKS- HAD FAMILY SHE HAD CHILDRENS THAT SHOULD HAVE BEEN TOLD ABOUT THEIR MOTHER MEDICAL HISTORY AND LIFE. I THINK THAT THE LAWS CONCERNING A INDIVIDUALS' MEDICAL HISTORY SHOULD BE KNOWN BY THE INDIVIDUAL AND FAMILY. MANY TIMES YOU THE PERSON HAVE A HARD TIME TRYING TO GET YOUR OWN MEDICAL HISTORY GIVEN TO YOU BY THE DOCTORS YOU SEE. MANY TIMES OTHER PEOPLE SUCH AS JOBS AND OTHER MEDICAL PRO- FESSIONAL CAN GET YOUR MEDICAL RECORDS AND YOU CAN'T, EVEN LAWYERS.

    Posted by Vera Chaney on February 1,2010 | 04:34 PM

    Wow this was an amazing piece that took a lot of fascination and dedication!! I will definitely read this book!!

    Posted by liz smith on February 1,2010 | 04:34 PM

    Well, humans were to live forever anyway. If you open your bible instead of waiting on mankind to confirm things that our Creator has already told us, you would really learn alot.God gave Adam and Eve a perfect human body they would've live forever if they obeyed Him, death was the punishment for their disobedience.

    Posted by Mia on February 1,2010 | 04:34 PM

    *You learn something new everyday, but this is something amazing. Unlike too many front page stories this one actually is important. Words couldn't express the significance of cells that could outlive the life span of any human being. Although, they should be compensated in some way whenever the cells are sold, I hope the family knows there is something worth more than money taking place with their loved one. She's apart of history, and could live on for generations to come.

    Posted by Kiara on February 1,2010 | 04:34 PM

    This is one of the most interesting articles that I have ever read. I plan to pass on this information and I am looking forward to reading the book!WOW!

    Posted by Lei San on February 1,2010 | 04:35 PM

    Loved the article and I agree with the people who feel as though the family is owed money. This took place in the 1950's when science didn't have no where near the capabilities they have now. Her cells were not taken by that Dr. in hopes to one day,25 years later, fund a multi-billion dollar industry. Nor were they taken knowing they would be "immortal". I still think they should of atleast been given permission by her to take the sample. Who's to say she would of agreed to it? Would we have still been able to do all that has been done with her cells with out them? Everything happens for a reason. Although the fact that they did make money off of her cells should be taken into consideration. I beleive they should receive some kind of compensation seeing as they never really had permission to take and use her cells to begin with. The family should be proud to know that their mother's cells have been used in numerous ways to save lives today.

    Posted by Cesilia on February 1,2010 | 04:35 PM

    I am a scientist and i think this article was very poorly written. First off, no cell is immortal, but the cell line can be able to continuously replicate itself (thus more are created as more die) Secondly, People who donate cells, blood, etc.. to science should not have any say in what research the cells are used for because they do not have the education/ background to make or be apart of that decision.

    Posted by Paul on February 1,2010 | 04:35 PM

    I actually heard the story about Mrs. Lacks many years ago and thought it would make a great documentary film. I actually found it disturbing and disagree with the author.
    To me the use of someone's essence without consent, regardless of leading to some great gains in the science/health field, is ghoulish. Forget the billion dollar industry it has spurned, it is like stealing part of her soul over and over again. Sugarcoat it however you wish, but it is clearly another example of the poor and uneducated Black being taken advantage of and blantanly deceived.

    Posted by Jonathan D. Wray on February 1,2010 | 04:35 PM

    This story is extremely interesting. I don't even like science, yet I'm still interested.

    Posted by Daneshia on February 1,2010 | 04:35 PM

    I hope the family receives compensation. I believe it should be expected.

    Posted by on February 1,2010 | 04:35 PM

    very interesting! great job!

    Posted by Jen on February 1,2010 | 04:35 PM

    that was good i like that

    Posted by michael ward on February 1,2010 | 04:36 PM

    This story is incredible. I'd definitely be interested in purchasing and reading the book. ..Sash La'ki..

    Posted by Sash La'ki on February 1,2010 | 04:36 PM

    Xtraordinary story; Timeless value

    Posted by Kyle LL on February 1,2010 | 04:36 PM

    The Family should be proud that a part of their mother has done so much good and saved so many lives. Why is everyone so sue happy? We live in a very sad world, and people wonder why healthcare is so expensive when every day people are being sued for just trying to do the right thing.

    Posted by apey on February 1,2010 | 04:37 PM

    Another story about subtle racism in America, and when the truth was nearly discovered, the "facts" were changed. Millions in profit made as the result of victimizing unknowing Black Americans while the family of Henrietta Lacks starved! A book well worth reading!

    Posted by C.D. Williams on February 1,2010 | 04:37 PM

    I noticed the comment about "lawsuit", everyone wants to sue someone these days, don't they? Ridiculous

    Posted by Cynthia on February 1,2010 | 04:37 PM

    Very good story. I worked with that cell line once in college and have always wondered where it was derived from. I hope that her surviving family get something for the huge impact that she had on drug research.

    Posted by JWilliams on February 1,2010 | 04:37 PM

    I find it interesting that there are no religious responses to this great book. Are we getting closer to understanding imortility?

    Posted by on February 1,2010 | 04:37 PM

    Interesting article. One woman made such important scientific discoveries possible. By "immortal cells" there's something sad about that. It just meant that the reason why her cells are still alive today is because it's scattered around various laboratories throughout the country and is being taken care of by scientists who still use it for their research. I hope that Henrietta Lacks' family get some kind of compensation, considering that the cells were taken without her permission, not donated, and the fact that companies who sold HeLa cells made billions. But from what I read in another article the family didn't even get an apology.

    Posted by Camille on February 1,2010 | 04:38 PM

    AMAZING STORY! SOMETIMES DOCTORS DO WHAT THEY HAVE TO FOR THE SAKE AND PROGRESS OF CLINICAL STUDIES.VERY PROUD OF THE FACT THAT THE WOMEN WAS REMEMERED AND THE STUDY WAS NAMED AFTER HER.

    Posted by on February 1,2010 | 04:38 PM

    I feel that the Medical Society, The United States Government, and Us. The People in which this lady not knowing for years paved a way to save the lives of many people of all races. Myself would like to thank her and her family for the contribution that was given to us. THANK YOU...

    Posted by Jeph on February 1,2010 | 04:38 PM

    1)I personally would be scared to work on immortal cells. Ever heard of the tower of Babel?

    2) What difference does it make that she was black?

    3) If the cells were immortal, why did Henrietta die?

    Posted by Micheal W on February 1,2010 | 04:38 PM

    That story really caught my attention! It's alot that we don't know about our black history and every time I hear something like this...it makes me Very PROUD to know that we(black americans)contributed to the WORLD and helped all races further their lives.

    Posted by on February 1,2010 | 04:38 PM

    this is a wonderful story.. It does not supprise me that no credit was ever given to her or her family never recieved any recompense.It is no supprise that the tissue was taken and used without her permission..this is simply typical of the way blacks have always been discounted as valuable and worthy of decent treatment. Did she live a long life? I need to read the book.. thanks, Dona

    Posted by ' on February 1,2010 | 04:38 PM

    I am speechless.

    Posted by Kim Love on February 1,2010 | 04:39 PM

    What everyone needs to understand is that racism is just a reality for blacks. In the 1950's it was the cultural norm to totally disregard them. When scientists found out about these cells, the couldn't just tell everyone where they got them from. Their research would have been shut down. Most whites back then wouldn't allow a black to live across the street from them, let alone accept medicine derived from one if it would save their lives. They would rather die, those were the times. So the scientist only did what was normally done with blacks, used them for test animals. It wasn't considered a human rights violation or anything. Have any of you heard of the 'Tuskeegee Experiment?'

    Posted by Rob Berry on February 1,2010 | 04:39 PM

    Nice piece, although that woman is clearly mixed race.

    Posted by James on February 1,2010 | 04:39 PM

    Also noticed people talking about the doctors being greedy and profiting off the cells. True. Very true. But who would her family sue? The doctors family? Is that really fair to either family involved. That would be like someone suing you for something your grandfather did.

    Posted by Cynthia on February 1,2010 | 04:39 PM

    Henrietta Lacks died from cancer in 1951 and her family still has not received any compensation!! Read more here:

    http://www.npr.org/blogs/thetwo-way/2010/01/henrietta_lacks_unsung_contrib.html

    Posted by Michelle O'Brien on February 1,2010 | 04:39 PM

    Amazing. There is so much that man has to learn to understand the works of God. Most doctors are selfish and mean. How can anyone do something like that and not bother to let the family know? Please someone compensate and involve the family from now on.

    Posted by Mariah on February 1,2010 | 04:40 PM

    Wow! That was very interesting! I'm inspired to go buy the book to learn more. Great Black History piece! Kudos!

    Posted by Timica on February 1,2010 | 04:40 PM

    WOW , I have learned so musch is such a short Article, I can't wait to read the book

    Posted by Carol on February 1,2010 | 04:40 PM

    and they are good on toast!

    Posted by john hopkins jr on February 1,2010 | 04:40 PM

    WOW !!! Henrietta Lacks, is a very special Lady.and Jesus had specials plans and gift for the rest of us. I think this is so Beautiful.
    what a Beautiful Woman.

    Posted by Anna on February 1,2010 | 04:40 PM

    Not a book I want to read. Nobody knew that Hela cells would turn out to be so important when the sample was taken.

    Therefore the only story is that the sample was taken without permission, and what are the legal damages for that?

    I suppose tissue samples can be sold? Say, what, $50 (today's value). And what's the punitive damages for stealing a tissue sample? 100 times the value? So $5,000?

    Is that a story?

    What about the the treatment she received from the doctor? Was it good, proper treatment for that era?

    I will bet you anything this book doesn't explain the amazing tenacity of these cells, but is just a bunch of unrelated human uninterest, packaged as a story.

    But wasn't she a pretty woman then? That old cracked photo. And so sad she was so young when she fell ill.

    Posted by Heckster on February 1,2010 | 04:40 PM

    Thank you, Mrs. Lacks and family. I sure hope if they haven't been compensated, they will be now.

    This would make a great movie, I think. I will buy the book! CS

    Posted by christine on February 1,2010 | 04:41 PM

    My comment is directed to William Thomas. Why do you assume that Ms. Skloot's motives are exploitive? You can know nothing of her motives from what has been written in this very interesting article. Your comments throw far more light on your personality than they do on Ms. Skloot's.

    Posted by Will Strong on February 1,2010 | 04:41 PM

    VERY INTRESTING INDEED

    Posted by Byron N on February 1,2010 | 04:41 PM

    This type of treatment of Black people is not atypical. It occurs throughout the world due to the dominant world idea "White Supremacy". Read "Medical Apartheid: The Dark History of Medical Experimentation on Black Americans from Colonial Times to the Present"

    http://www.amazon.com/Medical-Apartheid-Experimentation-AmericMedical Apartheid: The Dark History of Medical Experimentation on Black Americans from Colonial Times to the Present ans-Colonial/dp/076791547X/ref=sr_1_1?ie=UTF8&s=books&qid=1265059988&sr=8-1

    Posted by JOHN W. G. BANKS III on February 1,2010 | 04:41 PM

    Litigation? Litigation for the sake of right or wrong? Impossible! It is all about money, money, money, and the perception of rights. This went all the way to the Supreme Court of California. This following is copied directly from Wikpeida. Then, as now, there was no requirement to inform a patient, or their relatives, about such matters because discarded material, or material obtained during surgery, diagnosis or therapy, was the property of the physician and/or medical institution. This issue and Mrs. Lacks' situation was brought up in the Supreme Court of California case of Moore v. Regents of the University of California. The court ruled that a person's discarded tissue and cells are not their property and can be commercialized

    Why? Well can you imagine the doctor asking his/her patient if he/she would like the cancer cells removed during an operation. Perhaps a doggie bag for the left over cancer cells to go!

    Posted by mike on February 1,2010 | 04:41 PM

    This story should be made into a big-budget film. With the right cinematic treatment, it would be an enormous success. Halle Berry would be perfect for the role of Henrietta Lacks and Oprah Winfrey should produce it. If it's done properly, Ms. Berry would probably win another Academy Award, and Henrietta's family could be compensated by the profits from the film. I hope they're already working on it.....

    Posted by jph on February 1,2010 | 04:41 PM

    For those of you asking if the family was compensated, please read this article http://en.wikipedia.org/wiki/HeLa

    I am no scientist but I would imagine that since her cells are immortal and so dominant that they contaminate other cultures, the cancer that she was suffering from would have been very difficult to treat. God rest her soul but the aggressiveness of her tumour actually turned out to be a blessing !!

    Posted by on February 1,2010 | 04:42 PM

    Wow! Amazing and she died? Cells are supposed to die after at least one day and if they don't and can live for so long than that means Henrietta should live forever because as long as there are cells that are active in your body you can live!

    Posted by Henry Ning on February 1,2010 | 04:42 PM

    Very interesting! What an amazing story to uncover. I would love to read the book!! I think the family should be given a public acknowledgement by the science community and awarded compensation for Henrietta's contribution to the history of Health and Science. Lift up Henrietta to the country and people she has helped without knowing. Henrietta, The book, the author and the family should be recognized on TV. A News Show, Oprah, 20/20. Something to spread the story even further. How blessed have we been as a people just for her cells use in the polio vaccine? She could not get enough recognition for her impact on us.

    Posted by Lori Ashley on February 1,2010 | 04:42 PM

    An excerpt from the book "The Immortal Life of Henrietta Lacks", by Rebecca Skloot is published in the Feb 2010 issue of OPRAH Magazine on p. 159, called "The Miracle Woman".....and states the book goes on sale tomorrow, Feb 2. Fascinating!

    Posted by Estelle on February 1,2010 | 04:43 PM

    Since Henrietta had children, they should be well compensated for her amazing contribution to science and medicine. However, Henrietta brothers should not profit from this.

    Posted by Becky on February 1,2010 | 04:43 PM

    Great story!! I am buying the book.

    Posted by John Hartsock on February 1,2010 | 04:43 PM

    what intrigued me about this article is that things like this could happen to increase the life span.. It was very disappinting in that it did not tell of any life -saving episode as a result of the use of this gene I DID READ SOMEWHERE THAT LIFE COULD BE EXTENDED TO REACH MANY YEARS BEYHOND THE 100, PERHAPS TO 500. BUT THEN THE BRAIN, UNLESS GIVEN THOSE GREAT INJECTIONS OF GENES. oH WELL, WISH I COULD GET SOME.

    Posted by mary j. sullivan on February 1,2010 | 04:43 PM

    Henrietta Lack's story is another piece of Black History. Just think of how many other people this has happened to.

    Posted by cvicham on February 1,2010 | 04:43 PM

    Good innovation.....................
    I pray that Henrietta's family is called up one day to share the big monies the HeLa cells have collected since the big discovery!
    Please post more of such Innovative stories because they are educative.

    Bless!

    Posted by Henry on February 1,2010 | 04:44 PM

    Very interesting.. Can't wait to read the book!

    Posted by Brenda Silva on February 1,2010 | 04:44 PM

    I recently read somewhere that 72% of household dust is actually skin. No relevance here maybe, but tissue exists with or without our consent.

    Posted by Dale Oldham on February 1,2010 | 04:44 PM

    This story really fascinated me to learn more about hela cell..it really reflects human greed for self..the word which is more influencing todays humans.

    Posted by karmat on February 1,2010 | 04:44 PM

    If her cells don't die, does'nt that mean she is immortal? That Henrietta would never experience old age and death? It has to be some kind of mystery for her cells to never die yet Henrietta died.

    Posted by Srini on February 1,2010 | 04:44 PM

    I can't begin to imagine the myriad emotions I'd experience if someone approached me and told me that the mother I had never know was alive in a petri dish almost 60 years after her passing. There's a lot of ways to look at this story. I choose to look at all of the medical miracles brought to us by scientists using this line of cells. I agree with others that somehow a foundation be established to assist her family. Bottom line, I assume that she did not sign a donor card as we have the ability to do today. When I'm gone, I hopefully can help others in ways that I cannot help them now.

    Posted by Craig Basiliere on February 1,2010 | 04:44 PM

    Another case of the "Exploitation of a minority"

    Posted by Barbara on February 1,2010 | 04:44 PM

    I don't think the family is entitled anything. It's not like they did anything to hurt Henrietta Lacks. I guess in hindsight they should have asked but maybe they did, how would anybody know? It's not like they had protocol on this type of stuff 60 years ago, nobody knew it would lead to something so extravagent. The tissue sample taken from her probably wasn't even noticable to Henrietta and was no inconvenience to her. They probably owe them like $20 for the tissue sample if that...

    Posted by Genetics on February 1,2010 | 04:45 PM

    Wow great article!!!

    Posted by on February 1,2010 | 04:45 PM

    We certainly can not bring to life the intention of the person who took the cells in the first place. The matter became complex the minute it was conducted discreetly. The only genuine thing one can do is thank the heavens for Ms. Lacks... And as for the family recieving money, they deserve something, only if procedures are carried out according to rules of the time of the deed. Lovely writing, informative piece!

    Posted by Travis Mabena on February 1,2010 | 04:45 PM

    This will be on my to read list. I had heard of HeLa cells but never realized that there was a person behind them. I just thought it was a type of cell developed for study.

    Posted by Millie on February 1,2010 | 04:45 PM

    RIP Henrietta

    Posted by on February 1,2010 | 04:45 PM

    I read about these cells many years ago and at that time they were referred to as "Micky Mouse" cells, I believe because of their shape. I still have the article somewhere. I had forgotten. Thank you for reminding me. Great story. I WILL buy the book!

    Posted by Arthetta Rasul on February 1,2010 | 04:45 PM

    Wow is right.

    However, the answer as to why they are immortalized has been known for 20 years: they are infected with HPV - Human Papilloma Virus - which is a known cause of cervical cancer.

    The person writing this book wasn't concerned with the scientific aspects of the situation but that's the answer.

    Posted by Joe Blow on February 1,2010 | 04:45 PM

    It just makes you wonder, what else do scientist do w/out our knowledge. And are they still allowed to do these types of experiments w/out our permission. And I am happy that the daughter was able to fill a little bit of the void.

    Posted by Laura on February 1,2010 | 04:46 PM

    I am a nurse--30 years now. These cells were taken from a cancerous tumor. Therefore, when these cells are reproduced, they should also contain the cancer virus. I don't believe I would trust any research done on them unless it was just cancer research. When you clone a cancerous cell---you get another cancerous cell!!

    Posted by Katrina Acton on February 1,2010 | 04:46 PM

    Amazing, I am trying to go into the medical field, not a doctor, mind you. But I think the book would be a GREAT read!

    Posted by Brandy on February 1,2010 | 04:46 PM

    Loved the piece.

    Posted by Sandy on February 1,2010 | 04:46 PM

    The family going after money for nothing on their part demonstrates just how low human morality can sink for a mighty dollar $. The earth will be much better off once humans are not part of the natural equation.

    Posted by Tony on February 1,2010 | 04:46 PM

    nice

    Posted by frank on February 1,2010 | 04:47 PM

    I agree with one of the comments above, her cells can't be immortal because all living things must die. However, cells such as these could possibly increas the life span of humans. It seems so trivial to have something as astounding as this without the thought of making life longer! I'm not sure if these cells would help; I'm not a real scientist that has studied them. But maybe they could be tested in this way. Maybe these cells are the key to longer life on earth. Maybe not everyone wants to live forever, however, most of us want to live much, much longer.

    Are these possibilities even coming to their minds? I'm only 18 but I'd like to learn if these things are possible before it becomes too late for me.

    Nice article. You've done a very good job. If you are able, please answer my questions.

    -Zachery M.

    Posted by Zachery on February 1,2010 | 04:47 PM

    The cells are immortal. Scientists DO know why they are immortal. The cells will never die as long as the sceintific community keeps culturing them. Although the cells today probably do not resemble the original cells exactly, because over time, as cells divide, they aquire mutations that still leave the cells viable.

    Posted by Alli on February 1,2010 | 04:47 PM

    Interesting story. I will definitely purchase the book. Will Henrietta's children, specificially her daughter, benefit financially from the book sells?

    Posted by Nesha on February 1,2010 | 04:47 PM

    The companies that made a peofit from her cells should give the family 10% of the profits as a sign of good faith. If not the family should suit them for half of all the money made.

    Posted by Stephen on February 1,2010 | 04:47 PM

    Great story! All of your hard work and research over the years has paid off. I can't wait to read the book. I think just about everyone who has read this story wants to know more. This should be on Dateline!

    Posted by Whitney on February 1,2010 | 04:47 PM

    I hope, Johns Hopkins company will give their dues to Henriatta's own family. They should be thankful they found an immortal cell with many usage through Herrietta's cell. They must give the credit to Herrietta's family. If they didn't give their "thank you gift" to her family, they should start now, or give Henrietta's surviving family a lifetime support. That would filled the hall of injustice Herrietta's family suffered all those years since the discovery of her cell.

    Posted by analie on February 1,2010 | 04:48 PM

    Why should the family get any money? Is it do to the fact they were poor? or is it some thing you would want if you had given a single cell, did given the sample make her family homeles, Is this lady who wrote the book going to give up profits to the family. or do you think see does'nt need to because she "was up front with everthing" Still a good story though.

    Posted by Jim on February 1,2010 | 04:48 PM

    An interesting story, worth reading, to be sure. Now, if any of you would like to improve your spelling, try writing, “my curisosity is piqued to the point of buying.” There are three kinds of peek: peek, peak, and pique. Look ’em up! (You might even find peke as a nickname for Pekenese.) Someone please tell me the difference between “purchase” and “buy.” Just trying to show off, aren’t you?

    Posted by George Kern on February 1,2010 | 04:48 PM

    Why do they need to be compensated? What happens to all the tumors, tissues, placentas, etc that are removed in a hospital. I heard umbilical cords are useful, do they keep them without anyones knowledge and use them? Would you then be entitled to compensation? Haven't a clue, just asking. One man's trash is another man's treasure?

    Posted by Shamar on February 1,2010 | 04:48 PM

    She was a "black"woman? If she had've been caucasian...would she then have been a "white" woman,or would they have called her an American woman? These questions make me ponder the condition of this country. Could've been an honest mistake but come on, what gives?

    Posted by Lefty on February 1,2010 | 04:48 PM

    THIS WRITER STATES FAMILY MAY NOT BE ENTITLED TO A BUNCH OF CASH AS A RESULT OF THOSE CELLS USED. I BEG TO DIFFER AS HENRIETTA DID NOT DONATED ANYTHING AS THE WRITER WROTE IT WAS TAKEN WITHOUT HER KNOWLEDGE YOU CANNOT COMPARE FAMILY, AND PATIENTS THAT HAD BEING INFORMED OF MEDICAL ISSUES AND MADE A CHOICE VOLUNTARILY. SAYING HER CELLS WERE NO MORE THAN A SPECIMENS IN A PETRI DISH SEEMS TO BE MORE THAN THAT THIS IS SOMEONES DNA BECAUSE THERE IS NO OTHER SPECIMENS IN A PETRI DISH THAT HAS LIVED FOR OVER 25YRS LONG PAST DEATH AND IS STILL UP FOR DISCUSSION THAT WE ARE AWARE OFF. WITHOUT THE STOLEN SPECIMENS THOSE EDUCATED AND DRIVEN MEN OF SCIENCE WOULD NOT HAVE HAD THAT SPECIMENS TO STUDY.with so much benefits this provides, how is it that the source was forgotten? AND LET'S NOT BEGIN TO REVIST THE ERRA OF 1950 WHEN RACISM WAS VERY PREVALENT. This is not about money that worry me is that someone went to a hospital to seek medical assistant and a part of her DNA was stolen for scientific use without her knowledge and some how some of us this because it has not happend to us that we are aware off its ok, then we speak about how uneducated and poor the families are.

    Posted by annmarierowe11@yahoo.com on February 1,2010 | 04:49 PM

    Thanks for this story. I found it very informative and interesting.

    Posted by Karen on February 1,2010 | 04:49 PM

    I like this article, but even so they shouldn't be compensated for anything. Thats like saying the indians should have all of America because they were orginally native to it. It's asanine to think that greed always seems to win out, which it seems like it almost always dose. Also racist, because we got it from a black women... can we get over some things that didn't happen in this decade (some people still harbor hatred even thou, they live really good lives with no white oppresion, it happend long ago, people are somehow angry against whites or other because of a dumb thing thats not any reason to hold too this day, people who weren't even around at the time), but in a long past one. First things first racism is such a ignorantly created word we are all one race, Mankind.This isn't dehumanizing anything, to have genetic tissue samples of people, unless taken to an extreme, this is not one of those extremes. Also I think it was the right choice to aquire that sample to save people of today and further medical knowledge to benefit all. All I'm saying no one is intitled to something as laughable as that of any ethnic group.

    Posted by Kirk Meitzner on February 1,2010 | 04:49 PM

    I would be interested to know if the longevity of the cell strain had to do with the fact that it was a piece of cancer tissue. I have long suspected that cancer cells are a physiological attemt at immortality, though not in any deliberate way. The mutation of telomorase, which regulates the number of regenerations, etc. Any ideas out there?

    Posted by Don Wall on February 1,2010 | 04:49 PM

    I started my laboratory research work at Johns Hopkins Hospital in 1970. And, shortly after Dr. George Gey died his laboratory was remodeled to be used as an electron microscopy facility. Many of the old tissue culture related materials, mostly parts of equipmen, lay in a heap on the floor just outside the door to this lab. As much of these items were historically relevant, i.e. prototype equipment that was hand made for Dr. Gey but later manufactured for all scientists interested in cell biology. I saved a hand turned flywheel, embossed with the name of Arthur H. Thomas Company. It was part of equipment used to gently aggitate liquid cultures within an incubator, but Mr. Thomas took the trouble to put his name on the flywheel. I later learned that this company started making microscopic and biological research equipment around the same time George Gey started doing his seminal work in Cell Biology, including growth of HeLa cells. I also picked up a beautiful mahogany motion picture film casset that had an ivory plaque for writing down what the film contained. I believe this film casset was one of the cassets used for the first time to document the movement of living cells in culture. In any case, I spent many hours toiling in the same space where Henrietta Lacks' cells grew and supported research all over the world.

    Posted by Arthur O. Anderson MD on February 1,2010 | 04:49 PM

    I do hope that Ms. Skloot will compensate the Lacks family through royalties of the sale of her book. Were the rights purchased, or was he family's ignorance of the broader issue exploited? It really is their story to tell, with permission and *fair* compensation.

    Posted by Denise on February 1,2010 | 04:49 PM

    I remember learning about the HeLa cells from my father a physist, when I was in college taking biology. I mentioned this to my professor and he said, "there was no such thing, it was just sensationalism." I hope he realizes now, that my question regarding, "if he had received his Ph.D. from Sally Struthers Univ?", was actually a valid one.

    Posted by TBeaumont on February 1,2010 | 04:49 PM

    There are "ANGELS" on earth and this story of Henritta Lacks confirms it; though she was long dead her cells lives on. Hope the medical researchers involved HeLa cells would now right the wrong of taken her cells without her permission, by compensating the living children of Henrietta.

    Posted by Angela on February 1,2010 | 04:50 PM

    It was fortunate for science to discover the immortal cells and since then many cell lines have been discovered. I'm sure this family did not have health insurance to cover what treatments she received so I consider it a wash!

    Posted by Donna Lasko on February 1,2010 | 04:50 PM

    Thank you, this is amazing and emotional to finally know that Mrs. Lacks gave so many of us the chance to be alive and live normally without polio as well as other diseases. I hope that President Obama will recongize Mrs. Lacks and her family with humanitarian awards and recognition. I am honored and grateful to Mrs. Lack and everyone within her family.

    Posted by Dale Guy on February 1,2010 | 04:50 PM

    This is a great story, I am greatful that someone uncovered this piece of history and the tremendous price that Henrietta Lack has paid for all humanity. Thank you for your contribution in revealing a piece of history that we need to know.

    Javon

    Posted by Javon Brothers on February 1,2010 | 04:50 PM

    WOW. This goes to show you, if there is a will there is a way. This women might of died from cervical cancer. I do want to buy the book to find out the actual science behind all this.
    I do want to suggest to everyone that is also interested in the story, or the science behind this to go buy the book or to at least check it out from you local library.

    Posted by Kiir on February 1,2010 | 04:50 PM

    I can't believe how greedy American's are, just because something good happened from some cancer cells her family think's they deserve compensation? If not Henrietta it would have been someone else. It's not like they did anything to be entitled to compensation. Also when you go in for surgery or whatever the tissues or organs or whatever is extracted/harvested, whatever it may be can be used for research or disgarded/thrown away.

    Posted by Greed on February 1,2010 | 04:50 PM

    I want to buy some Hela cells and make a clone.

    Posted by on February 1,2010 | 04:51 PM

    Wow, so who knew cells could last so long, did her daughter ever get any of her questions asnwered about her mother? Did her husband ever learn how to read? Was the family ever compensated for henriettas contribution to life, if it wasnt for her we wouldnt know what we know about cells today.....

    Posted by roschelle on February 1,2010 | 04:51 PM

    Biological Slavery...justified in the name of science.

    Posted by La Smith on February 1,2010 | 04:52 PM

    I am a nurse. Doesn't anyone understand that when you clone a cancer cell---you get another cancerous cell---only good for cancer research. I wouldn't want to take a vaccine produced from a cancerous cell---would you?

    Posted by Katrina Acton on February 1,2010 | 04:52 PM

    A very educational article.I had no idea a cell line had been alive so long.I think it is marvelous what scientist have learned from Henrieta's cells, but I do feel the family should get some compensation for all the knowledge that was gained from the immortal cells.I plan to find the book and read it.

    Kay R. Stephens

    Posted by Kay R. Stephens on February 1,2010 | 04:52 PM

    The people behind the HeLa cell story have only one thing in mind:GREED FOR MONEY!

    Posted by Vicente Estoque on February 1,2010 | 04:52 PM

    Thank you Mrs. Laks!! this is the example of how a single person can make a difference. It's also an example how ethical treatment of people and biological samples is of paramount importance. No one should be used for research without informed consent and the use of biological products must be strictly regulated. I hope the Laks family succeed in being compensated.

    Posted by htellesa on February 1,2010 | 04:53 PM

    Sounds like this book should be on Oprah's book list and possibily a documentary for her Oxygen station.

    Posted by jeanne on February 1,2010 | 04:53 PM

    This was just amazing and I applaud the writers tenacious and very curious nature.
    In response to a comment asking whether the family could possibly sue the doctor in question...well, this society is litigous enough without encouraging it any further.
    The family should be honored that their mothers cells helped the scientific community in any way.
    Boot straps people! Pull them up. They have no one to blame but themselves for living on the steet and living in poverty. There is no reason why they can't better themselves on their own. Looking for a hand up or hand out with that sense of entitlement is frankly old and boring.
    BOOT STRAPS! PULL YOURSELF UP!

    Posted by coastalgirl on February 1,2010 | 04:53 PM

    So, you are saying that polio vaccines etc... contain a part taken so many years ago from a tumor cell. What are the risks here of having carcinogenic elements in such a vaccine or other treatment products?

    Thanks

    Posted by Sam Gar on February 1,2010 | 04:53 PM

    What happened with the cancer? Are we all sick now?? Hmmm

    Posted by bruce on February 1,2010 | 04:53 PM

    Great article. Wow, she has a name. I just wonder how many more fascinating stories like these are out there. As a teacher, this is great news to share during Black History Month.

    Posted by Carla on February 1,2010 | 04:54 PM

    I'm still trying to figure out who released the fruit flys which lay eggs on people and never die, letalone how Henrietta's cells float on dust particles which may also be a contamination problem.

    Posted by ann coe on February 1,2010 | 04:54 PM

    I guess its just me but that couple reminds me alot of a UFO story about a couple that was abducted by UFO's a while back. I'll see if I can find that story and compare notes.

    Posted by felix on February 1,2010 | 04:54 PM

    Does this mean that Blacks ar genetically superior to ther races, since civilization began in Africa? I am not a scientist but I suspect this it true. This is a fascnating story that ultimately helped save maybe thousands of lives. If others have gained monetarily from this research, why not the family?

    Posted by Linda on February 1,2010 | 04:54 PM

    Looking back at the picture associated with the story and reading the comments, it seem interesting that some refer to the contributions from the "men of science" when the two lab techs are ladies. I guess much like Henrietta's, they too were not worthy of acknowledgement by some, only the "men of science".

    Regarding the story, the wonder of science and nature never cease to amaze!

    Posted by Michael on February 1,2010 | 04:54 PM

    Should also read just released: How Long Things Live, ISBN: 9780811736220 (Stackpole Books). Some organisms are said to be immortal in this book.

    Posted by Trish on February 1,2010 | 04:55 PM

    I heard of those cells during the 70's while in graduate school during cancer research. Being a black woman myself,I was very proud of the contributions this black woman cells gave to cancer research. I am happy that her family is aware of this and I hope they were compensated.

    Posted by Brenda on February 1,2010 | 04:55 PM

    Very interesting, if this was done legally why was their a need to hide her identity? Is it because?

    Posted by S.Sweet on February 1,2010 | 04:55 PM

    This was a great article. I would like to buy a copy of this book as well.

    Posted by Janine on February 1,2010 | 04:55 PM

    "I still," and "will always" find this story to be "absolutely and unbelievably" amazing and "beautifully outrageous!!!" (smile) I discovered Ms. Henrietta Lacks, in Harriet Washington's, "Medical Apartied", which is just a wealth of knowledge, concerning black people and the medical establisment in general!! It is simply "a must read" for "all and every" of us (blacks) who want to know "our true and complicated history" with the Medical Association.(ie. our "adversion", along with our "suspicion") with regards to the health profession. Yet sadly, our "profound contributions" to it, like that of Ms Lacks, still "goes unknown" to many of us, in the black comminity and in our schools!!! (sad, madd...) VIVA la, HeLa cells!! SHE "HAS (Henrietta) SAVED MANY" LIVES INDEED!!! (smile, smile)

    Posted by Kim C. on February 1,2010 | 04:55 PM

    I read of Ms. Lacks in the early 70's while working at UMDNJ, the Medical School in Newark, NJ. I shared this information with many friends and family over the years only to be told by a medical "professional" some time ago, that I was incorrect about my reference of HeLa cells and Ms. Lacks' name. I appreciate that the author has done the extensive research and published the book so that the correct information can be better understood by all. It is my sincere hope that Ms. Lacks' family be reimbursed and granted some legal rights to the profits that have been earned because of Ms. Henrietta Lacks contribution to medical science.

    Posted by H. F. Abdul-Ghani on February 1,2010 | 04:56 PM

    We read the correct historical report concerning Henrietta Lacks contribution to medical science; interesting. In an effort to continue the quest for scientific fairness, how... could the richly funded Smithsonian allow the unretouched photograph of the young Henrietta Lacks to be posted on their web-site before it was restored. Someone at the institue should have repaired that photo before it was posted. After all, a middle school student can use Photoshop to repair photo damage. Shame on you!

    Posted by m b saunders on February 1,2010 | 04:56 PM

    Some observations: The article stated doctors took peoples cells, not just hers. Hers happened to be the ones that worked. The theory of 20 years was finally proven. YET They apparently took cells from whoever they could, not discriminating! Good story. She should be honored and credited with helping mankind. The family should receive some money of course. This is just an article, I doubt the whole story will be shared here.

    Posted by carolina on February 1,2010 | 04:56 PM

    If her cells were used to create an "immortal cell line",which in turn created many of the extraordinary medical breakthroughs of our time, then wouldn't it be possible to create a youth/immortality serum of some sort from the same cell line? I know it may sound crazy to some people, but if you stop and think about the "Star Trek" type technologies that have actually been created for actual use in the medical field, by civilian society and by the U.S. Government/Military that were at one time thought to be only fantasy and make believe such as: cloning,C.A.T Scans,3D X-rays, ultra sounds, speech recognition software etc. Then why isn't immortality or extended youth right around the corner? I know what you all must be thinking (cloning is a form of immortality)while this theory may be true, it's only your cells and DNA that may possibly live on, but our souls, memories, and the other things that make us who we are as individuals can't yet be cloned, at least not to our knowledge.

    Posted by Michael Beard on February 1,2010 | 04:56 PM

    a very interestingstory for science i would love to have the book please let me know where to get it

    Posted by donna on February 1,2010 | 04:57 PM

    as an rn of many yrs.i have 2 different thoughts about this article. as one of compassion and fairness. on a human, emotional level, COMPENSATE this family!

    on a scientific level, i am very curious it was cancerous cells that have survived. and why this type cell was extracted and cultivated versus the normal cell. both were available. that is very curious to me and think that is profound in and of itself.

    the author had the mind and sense to have known the great importance of this seemmingly, benign happening and the enormous ramifications, as a result. i commend her and as others, will read the book.

    Posted by shirley on February 1,2010 | 04:57 PM

    Wonderful story. Would love to read more - the book perhaps!! Any infor about where to purchase will be greatly appreicated.

    Posted by Louise on February 1,2010 | 04:57 PM

    Nice! I will be purchasing the book! I can't wait to read it.

    Posted by Gail Johnson on February 1,2010 | 04:57 PM

    cool but i want 2 hear more about what they have done with the cells!!!

    Posted by samantha on February 1,2010 | 04:57 PM

    Absolutely amazing. Makes me wonder about evolution?

    Posted by ed jordan on February 1,2010 | 04:58 PM

    What keeps the cells alive? They are not attached to a food source...blood? Did the family ever recieve compensation?

    Posted by Glenn Fulcher on February 1,2010 | 04:59 PM

    To all interested, The title: The Immortal Life of Henrietta Lacks by Rebecca Skloot, will be released on February 2, 2010. You may pre-order today from Amazon.com in book in formats including Kindle.

    Posted by Vanessa on February 1,2010 | 04:59 PM

    I don't think the family should get any money for her mother's tissue. This will cause a uproar in people demanding money for tissue and body parts that are done on a volunteer/donation basis. I'm wondering if they can get a lawsuit do to the fact the tissue was never taken with her permission. Perhaps they can get some royalties from the book. It would be great if her fame could change the course of the generations of poverty in the family.

    Posted by Virginia on February 1,2010 | 04:59 PM

    very nice peace. i'm 16. and yes i enjoyed reading that very much to the last word. it would be nice to learn more about stuff like this in school.

    Posted by caleb on February 1,2010 | 04:59 PM

    Wow! This story is nothing short of amazing. I definitely will be reading the book.

    Posted by Lisce on February 1,2010 | 04:59 PM

    In 1951 a tumor removed from a patient was not handled with as much "care" as we do today. When a tumor is removed these days it is sent to a Pathology Lab to determine what kind of cancer it is and is cataloged and sometimes stored. If in 1951 it was sent to a Lab, that Lab was either on site or affiliated with the hospital. After the Pathology was completed, the tissue was probably destroyed. So sending a piece of a tumor to a Research Lab, replicated by Scientists and subsequently sent to Outer Space ! How exciting a story is that ! As for the Billions of Dollars made from these cells ? People should focus on the way we can help each other and focus less on the rewards or recognition we receive ! Here is a spoiler for some people, you may spend most of your life not recognized or rewarded for anything that you do.

    Posted by Karl Scoville on February 1,2010 | 05:00 PM

    What a great story!I would like to know more about this story!

    Posted by James Jones on February 1,2010 | 05:00 PM

    We are talking about the 1950's aren't we?! Ironically white Americans were unaware that a Black womans DNA was being used in vaccinations that Im sure the majority of Americans received. I think that's the reason for the secrecy. People would have rather died of Polio than received a drop of black cells injected into their bodies. As for compensation, they clearly said her cells were "TAKEN", which means she didn't give consent. So her family is entitled some type of compensation when drug companies have made BILLIONS w/ a "B". Overall I thank the author for exposing another American history cover-up.

    Posted by Paperz on February 1,2010 | 05:00 PM

    I read about this historic finding in grad school and found it amazing. It pleases me to learn that someone researched the story further and that the family was able to be compensated for what has been stolen from them. Does her offspring have the same cells? How does scientist explain this finding? This adds to the theroy that black people were the first on the planet. Interesting

    Posted by on February 1,2010 | 05:00 PM

    @C. Frasier The cells are immortal not because one cell lived forever. It was because the cells are able to grow (i.e. multiply) forever.

    Posted by B-Net on February 1,2010 | 05:00 PM

    One thing that gets lost in the name of science, and business, is a focus on--and insistence on--Honor. Without honor, so much can (and does) deviate from what we know to be right and good. I'm not talking about religion. All traditions, as well as atheists, know what the word 'honor' means. It's just that we too often ignore it, even laugh at it. We will need a sense of honor more and more as the potential to be heartless in the name of science tempts us more and more. It takes work.

    Posted by M D Reser on February 1,2010 | 05:00 PM

    i don't see why people think ANYTHING is owed the family, they didn't even care until AFTER they found out money was even involved. What do you think happens to tissue and body part donations? someone out there WILL make money off of what is donated, or used in studies. Every single study of cells, tissue, blood, viruses, illness, disease, bone was done with SOMEBODY'S body part, are all of them owed anything? the family didn't even have anything to do with it.

    Posted by david peele on February 1,2010 | 05:01 PM

    Does she have any living relatives that can be paid from her contributions?

    Posted by Ephraim on February 1,2010 | 05:01 PM

    Does she have any living relatives that can be paid from her contributions?

    Posted by Ephraim on February 1,2010 | 05:01 PM

    Beautiful piece! Hope the family has or will be compensated after all these years.

    Posted by on February 1,2010 | 05:02 PM

    Thanks to Miss Lack our medicine went from medieval to modern. We as a species owe her a great debt of thanks. I realize her family should be compensated in some way, but let's not forget the time frame this took place. It was probably done for the sake of research and curiosity. The big "WHAT IF". I hope it doesn't get ugly, this is a great story.

    Posted by linann on February 1,2010 | 05:02 PM

    Thanks to Miss Lack our medicine went from medieval to modern. We as a species owe her a great debt of thanks. I realize her family should be compensated in some way, but let's not forget the time frame this took place. It was probably done for the sake of research and curiosity. The big "WHAT IF". I hope it doesn't get ugly, this is a great story.

    Posted by linann on February 1,2010 | 05:02 PM

    So, the filthy rich doctors stole priceless organ tissue from a dying woman without her permission, and made zillions of dollars off it. Meanwhile, the dirt poor family never got a dime and continues to get screwed. Yeah, real swell human relations story.

    Posted by Alien Gene on February 1,2010 | 05:02 PM

    Great Story! If I had more money I would make a movie out of it, using beyonce as Henrietta Lacks. For I already see it, it would even be nominated for Academy Awards. The story is remarkable and its part of the American history. Great movie involving the high end upscale people and the low end people, together in harmony as we are all connected in the great circle of life.

    Posted by Smaily Daniel Vasquez on February 1,2010 | 05:02 PM

    Recovering the Sacred, Winona LaDuke Blood, Academia, and Human Genetics Page 113 Approached by what you believe are some trusted researchers who propose to do a study of the incidence and possible solutions to diabetes, hundreds of community members donate blood. Some are given general consent to sign, while others receive only an oral explanation of the project. Those blood samples disappear into the laboratories of Arizona State University, along with copies of other medical records, taken surreptitiously without anyone's approval. A decade later, Carletta Tilousi, Tribal Chairwoman of the 65 member Havasupai Tribe, is shocked listening to a doctoral presentation reporting on the use of Havasupai blood samples to uphold the Bering Strait Theory, directly challenging Havasupai oral history, The tribe's blood, which they thought they gave to end the diabetes epidemic in the community had found its way into a wide range of genetic research in numerous labs, including those at Stanford University and in the private sector pharmaceutical industry.

    Posted by Derrick Rainbow on February 1,2010 | 05:02 PM

    People should really read this story. The year is 1950 and the family is poor and uneducated. Some say that the family was money hungry. I disagree and say the family didn't understand and just signed their x and recieved money for their blood and cells.

    Posted by john r on February 1,2010 | 05:02 PM

    So,problems don't arise in research by using tumor cells?

    Posted by Andi on February 1,2010 | 05:02 PM

    So,problems don't arise in research by using tumor cells?

    Posted by Andi on February 1,2010 | 05:02 PM

    Great article! The more I agree that all things created by God has its purpose. That blacks have been created that other colors maybe saved?

    Posted by Fe de Luna on February 1,2010 | 05:03 PM

    Is it significant that these were tumor cells ?

    Posted by D. Alan Curry on February 1,2010 | 05:03 PM

    haha awwwwwwwww this story is so cute=] very inspirational=]

    Posted by stephanie on February 1,2010 | 05:03 PM

    very interesting!

    Posted by george briggs on February 1,2010 | 05:04 PM

    How much more haven't they told us?

    Posted by Yo. D! on February 1,2010 | 05:05 PM

    What I do not undertand is the greed of people, thinking that everything has money value. If H.L. would have been my mother I just be proud of her and I will not be asking for money, mo matter what. Science is for all human beings, with out that, millions of us would be dead by now.

    Posted by Jonathan on February 1,2010 | 05:05 PM

    This story was very thought provoking. Although I am sure that her son’s didn’t go about it the correct way, I do agree with them and I believe that if it is making others rich the family should be paid too.

    Posted by Tanya on February 1,2010 | 05:05 PM

    The cells were propagated by George Otto Gey without Lacks' knowledge or permission (neither she nor her family gave permission)[1] and later commercialized, although never patented in their original form. Then, as now, there was no requirement to inform a patient, or their relatives, about such matters because discarded material, or material obtained during surgery, diagnosis or therapy, was the property of the physician and/or medical institution. This issue and Mrs. Lacks' situation was brought up in the Supreme Court of California case of Moore v. Regents of the University of California. The court ruled that a person's discarded tissue and cells are not their property and can be commercialized.

    Posted by Jim on February 1,2010 | 05:05 PM

    great story i am only confused about why would the family want money. i would give my life never mind canceros cells to help my fellow man.

    Posted by sparky on February 1,2010 | 05:06 PM

    great story i am only confused about why would the family want money. i would give my life never mind canceros cells to help my fellow man.

    Posted by sparky on February 1,2010 | 05:06 PM

    This story is very intrerestig,it also shows the how our Scientific community has it's own agenda,without regard or regret for Henrietta's family!AS FAR AS I AM CONCERN IT'S JUST ANOTHER WHITE WASH!What other secrets are they harboring?GOD BLESS AMERICA?I HOPE SO...!

    Posted by ROBERT BELLA DEVEGA on February 1,2010 | 05:06 PM

    I don't feel the family should be compensated at all.None of them were even interested until the word "money" was involved.Sounds very selfish to me.
    And if it weren't for cell research half the people here on earth wouldn't be here today.
    Just one womans opion.

    Posted by T.Smith on February 1,2010 | 05:06 PM

    at the time im learning about cells. it's impossibe that there would be immortal cells. all cells die, and new ones are born from that exiting cell. one part of the cell theory is that ALL cells come from cells that are really exist. its like reprodution. when you born you come from two cells, then that creates some cells, then reproductions comes in agian, more and more cells come. ALL cells die, but new cells are born. this subject to me, is easy! If any kind of scientist who has found out about the immortal cells, they ought to be aware of the cell theory!!!! I don't know everything about cells, but im aware of ALL the cell theory. plus if there were immortal cell, the living object would have to be immortal also. Is there any proof?

    Posted by anonamies on February 1,2010 | 05:06 PM

    Micheal Herring.....I am sure Mrs. Lacks' family is extremely proud to know that even after her death, she has contributed greatly to mordern medicine and science. However, the fact still remains that Mrs. Lacks' nor her family had knowledge or gave consent for her cells to be used for research.

    As far as I am concerned, no amount of money can compensate this family for their loss and the gift that she has given the world of science and medicine.

    But from an ethical standpoint, it was wrong!..POINT BLANK, PERIOD DOT! So with that being said, the family should be compensated.

    Posted by Carol M on February 1,2010 | 05:06 PM

    at the time im learning about cells. it's impossibe that there would be immortal cells. all cells die, and new ones are born from that exiting cell. one part of the cell theory is that ALL cells come from cells that are really exist. its like reprodution. when you born you come from two cells, then that creates some cells, then reproductions comes in agian, more and more cells come. ALL cells die, but new cells are born. this subject to me, is easy! If any kind of scientist who has found out about the immortal cells, they ought to be aware of the cell theory!!!! I don't know everything about cells, but im aware of ALL the cell theory. plus if there were immortal cell, the living object would have to be immortal also. Is there any proof?

    Posted by anonamies on February 1,2010 | 05:06 PM

    Sounds to me like she was alot more than just a poor tobacco farmer, God had a great plan for her, she just didn't know it.

    Posted by Virginia Melius on February 1,2010 | 05:06 PM

    Awesome. It would give me great joy to be gone from this world, and leave a part of me that is alive always.

    Posted by Eva on February 1,2010 | 05:06 PM

    Very interesting piece, and what a wonderful research done. Like to know more about it.

    Posted by Janaki Dronamraju on February 1,2010 | 05:06 PM

    WOW!! HeLa cells, that has benefited the world. Amazing. I too have heard of them but did not know what the acronym meant. Looking forward to the book. If anyone profited from Henrietta Lacks cells, then I believe her family should be compensated also. None-the-less, this story is amazing.

    Posted by KB on February 1,2010 | 05:06 PM

    Guys, there is a reason no one knows if the family was compensated. YOU HAVE TO BUY THE BOOK AND READ IT.

    Posted by Anflo on February 1,2010 | 05:06 PM

    This is only the beginning of the debate regarding cell, tissue and organ harvesting.

    Donors are seldom compensated in the US. But the donated organs and body parts become part of an immense commercial enterprise, gaining value each time they are sold. Perhaps a VAT (Value Added Tax) should be charged for each sale of biological detritus and the proceeds used to fund healthcare for the poor.

    Posted by D Washington Irving on February 1,2010 | 05:06 PM

    I loved this article very interesting :)

    Posted by on February 1,2010 | 05:06 PM

    Having been a patient in clinical trials of a cancer vaccine, I knew that volunteers have to sign away (and forget) any personal ownership of their cells--of any kind--that are part of a study. This book about the first successful donor of human cells is really about ignorance in American schools. It's a great, surprising story. I want to read it, too.

    Posted by Gary Ward Scott on February 1,2010 | 05:07 PM

    Do you have any idea how ignorant, greedy, and uneducated you sound when all you have to say is "Did the family get the money?" What did they do to deserve any money whatsoever. If they wanted to develop the technology then maybe they should be rewarded for that. Sorry.

    Posted by John on February 1,2010 | 05:07 PM

    dude i like never knew there was cells that lived forever. does that mean that if she had ived she would have lived forever...like if she never was sick??

    Posted by sarah e. on February 1,2010 | 05:07 PM

    I knew about this years and years ago. Read Medical Apartheid: The Dark History of Medical Experimentation on African Americans from Colonial Times to the Present by Dr. Harriet Washington-- many untold but often publicly documented stories that make Tuskegee medical experimentation seem minute in comparison

    Posted by Janell on February 1,2010 | 05:07 PM

    Dr. Amber Bokhari's comments are very much what I was feeling. I am sure this woman would be moved to tears knowing her contributions to science made it possible to help SO many untold numbers of people fight disease. This is a moving story and a fascinating one. I understand the family feeling like perhaps they should have been compensated. I don't understand the people who think it was racist or malicious. The doctor didn't know when he took the cells to study what would come of it. It was short of miraculous that these cells just happened to respond in the way they did when no others before them would. If any of my cells could be of help in such a way, I would be so happy to help. There would be an immense peace from knowing I somehow contributed to curing or preventing a disease.

    Posted by MissNovemberTuesday on February 1,2010 | 05:07 PM

    Great story & I think this will even make a great movie.

    Posted by Tandie on February 1,2010 | 05:07 PM

    HELLO BLACK HISTORY MONTH-- GREAT STORY

    Posted by Howard on February 1,2010 | 05:07 PM

    This is an intricate story about how humans need each other. As a human race, we should view this story as an example of how one of us gave something to all. Without knowing maybe, but that doesn't erase her gift. Mainly, we just need to understand we exist because we are all connected. Even when we have never met. We have the capability to be an amazing race, species, or whatever you want to label us.

    Posted by Rael K Coleman on February 1,2010 | 05:07 PM

    What impact on telemores does HELA cells have? Seems they have an unlimited supply otherwise they would die after replicating and using up the usual limited supply.
    If that is the case there is the possibility for immortality if science discovers how HELA cells do not run out of telemores and can treat others to maintain their supply.

    Posted by Ann Amos on February 1,2010 | 05:07 PM

    Great Article!

    Posted by Larry Tomas on February 1,2010 | 05:07 PM

    This was very interesting.. but i love how everybody posting on here thinks they know everything about everything. TRUTH is.. you don't so don't even try to act like you do. scientists who observe these cells don't even understand why they have lasted so long. so how do you think you will? i mean just imagine how complex this actually is. this is just one of those things no one will ever be able to explain. freaks of nature.

    Posted by Chris on February 1,2010 | 05:07 PM

    Awesome!!! very interesting and love to read the book.

    Posted by Liliana on February 1,2010 | 05:08 PM

    Awesome article and dedication on the writer's part to bring some answers to Henrietta's family.It is about closure,it is about peace and it is about simple human compassion. I don't see at all where a racial issue was ever the motive. It is going to be made a racial matter now because that's just what some people want others to believe. It was all in the name of science and medicine. The race of the patient wasn't the purpose behind the research. Should't we all recognize that science and medicine isn't racial, ii's about using the knowledge that our higher power has given us to help others.

    Posted by ladyfoxx on February 1,2010 | 05:08 PM

    That was a great story. I usually get bored and stop reading half way through but you kept my attention until the end. Not only is it a great piece about science but hopefully it will teach others that black and white is just a color and we are all the same inside. Thanks, Ellen

    Posted by E Smith on February 1,2010 | 05:08 PM

    Hello, I BELIVE THAT THE FAMILY SHOULD BE COMPENSATED BIG TIME. ALSO, I WONDER IF A MOVIE IS THOUGHT ABOUT.
    Oh wow, this woman gave the ultimate sacriface and each one her children and grands should be millionaires

    Posted by Annie Fryson on February 1,2010 | 05:09 PM

    Intersting case. This is not the first time body parts were used withour authorization, and I'm sure it won't be the last.

    We should put all racial attituds out of our heads. The largely social construct we call race has nothing to do with this case. All those cells grown from other cells never dealy with prejudice or discrimination, never were called names for something over whicvh they had no control.

    I would point out that using the cells withour permission may have been wrong, depending of what kind on informed consent was givin to the original surgical procedure. I see no way in which the measure of damages is related to the later use of the cultures, which, after all, could have come from any one other of the billions of humans on Earth.

    Posted by Lou Gots on February 1,2010 | 05:09 PM

    I've worked in the construction field for the past 7 years-this piece makes me want to change careers into the medicine world! This story is very unique.

    Posted by trin on February 1,2010 | 05:09 PM

    It's great and important for mankind

    Posted by Hurtz on February 1,2010 | 05:09 PM

    I would hope that the other future doctors know how to be ethical in their profession. Perhaps at the time that doctor that took some sample cell from Henrietta's didn't know about medical ethics. Perhaps, his motivation for his actions is for the good of human kind. To discover a cure, but then greed always play an important part of people's lives that no sooner they will use that opportunity to make money out of something, be it a sample cell.

    Posted by emy on February 1,2010 | 05:11 PM

    Immortal cells sounds like something out of sci-fi, at first... even so, I don't think Mrs. Lacks would object. She would be proud that she could make such a contribution to medicine... even after the grave.

    Posted by Dave on February 1,2010 | 05:11 PM

    Many (if not all) courts have determined, that an individual does retain a legal interest in excised tissue (tissue seperated from the body) where there is no expectation that the tissue will be returned to the donor. This case is similar to MOORE v. The REGENTS OF THE UNIVERSITY OF CALIFORNIA (1990), a California case, for instance. The family might be able to go after the doctor for failing to properly disclose how the cells would be used, but not for "conversion" (taking without permission). It isn't really a racial issue... people will take from other people, regardless of race, when the law dosn't prevent it. In this case, the public interest in letting this kind of testing continue was probably so great that the court didn't want to extend ownership rights of property to the cells from one's own body in this case. Finding that doctors needed to provide extensive counseling or return tissue samples to donors would have had significant effects on organ donation, biological research, and the practice of medicine in general.

    Posted by TDM on February 1,2010 | 05:11 PM

    Amazing article! I'm not sure if it was mentioned above, but I would like to point out that all cancer cells are "immortal." Cancer cells, unlike normal cells, do not respond to certain extracellular signals and do not exhibit density-dependent inhibition. This allows the cells to grow into the huge mass of mutated cells known as a tumor. Also, it should be noted that when normal cells replicate their DNA a portion of the DNA is spliced off, which makes the DNA strand much shorter. For this very reason, DNA is equipped with telomeres, which are repeating sequences of nitrogenous bases that protect the valuable bases from being spliced off during replication. Years of DNA replication degrades the telomeres, which causes the cell to die. Cancer cells, however, contain the enzyme telomerase, which rebuilds the cell's telomere. In effect, a normal cell replenished with telomerase would be "immortal" like a cancer cell. If scientists could figure out how to get the human body to keep producing telomerase, a person could - in effect - live forever.

    Just a little bit of interesting information I learned - and yes, it is all correct. No wikipedia here!

    Posted by Lexi on February 1,2010 | 05:11 PM

    That was a very interesting story. Science is amazing the things they've accomplished. In the 1950's A Black woman or man were lucky to get a doctor to even look at them let alone treat them, Whether the Dr. in 1951 realized the implications of what he was doing would he have still choosen Mrs. Lacks Cells or cells from someone else or because of the way things were racialy and the condition of Mrs. Lacks was she nothing more than an experiment did the Dr. know what he was doing? it seems to me you could do this with cells from anyone it just happened to be Mrs. lacks, There is alot of questions to be discussed about this case. And if the family does deserve compensation where should that come from the 'Original Dr.' that has probly passed because after him other people would have paid for these cells from the person or persons that had them by now these cells have been bought and sold thousands of times, Also the cells they have today would be 'ancestors' of the original cells not acctually the cells that were removed from Mrs. lacks in 1951 no matter what the case Henrietta Lacks has helped science perhaps more than any one person in History and all without her knowledge. It is a great story and I hope her family can move on realizing at the same time there mother helped perphaps Millions of people some day Billions, Wow pretty kool bragging rights at the least.

    Posted by D.G. on February 1,2010 | 05:11 PM

    Now someone else will make money off of those cells, after the doctors and researchers have for years. Henrietta lives on in many bank accounts and the fame and fortune of others. She and her family get nothing.

    Posted by Robert on February 1,2010 | 05:12 PM

    Did anyone notice that the brothers of Deborah were not interested, UNTIL they thought they could make some money.

    Interesting how money does that very thing.

    If no money could be made, would they still be interested.

    Bet NOT.

    Posted by Roger on February 1,2010 | 05:12 PM

    Verrrry interesting! It's sad the family wasn't interested until there was money involved. And so what if she was black. She was a women with cancer and we should be thanking the doctor who removed her cells for further research and the hundreds of thousands of doctors and other researchers that did so much with so little. I'm sure HeLa wasn't only one in history that this happened to.

    Posted by Ron on February 1,2010 | 05:12 PM

    Is Rebecca Skloot sharing the proceeds from this book with the Lacks family? If not, what is the ethical difference she sees between exploitation of the story and exploitation of the cells?

    Posted by jerry l on February 1,2010 | 05:12 PM

    i hope soon they will find a cure for the neuro degenerating disorder.not that i don't believe in the bible's hope of everlasting life on a paradise earth,but i would like to see my 20year old son without this condition till this paradise comes.actually i wish health for everyone.but if it does not happen,be strong people,there is going to be a time when no resident will say 'I Am Sick'Isaiah 33;24 This is a promise from GOD.im sure we can count on him.

    Posted by dolly on February 1,2010 | 05:12 PM

    nices good info to know!

    Posted by veronica on February 1,2010 | 05:12 PM

    Wow... how amazing... and how brillient! amazing what a reasercher can do and how so many have been helped...

    Posted by Mary Ann Jones on February 1,2010 | 05:12 PM

    very interesting findings and research! It's often true that many times things done even with best intentions may not go according to plan, but it is obvious that HeLa cells were of importance during life and after death. I wonder how many more persons have cells in use like this to date. Maybe a sure for some diseases can be found this way.
    great story!

    Posted by Jo on February 1,2010 | 05:13 PM

    nices good info to know!

    Posted by veronica on February 1,2010 | 05:13 PM

    THIS WAS A GREAT READ AND I WOULD LOVE TO READ THE BOOK AND I FEEL IT WOULD BE A GREAT MOVIE ONE DAY

    Posted by michelle on February 1,2010 | 05:13 PM

    Excellent article. Very informative. Well done!

    Posted by alsin on February 1,2010 | 05:14 PM

    I do believe that a lot of cancer cells are immortal because the telomeres don't get shorter when the cells divide. Probably one of the reasons why cancer is such a hard disease to cure.

    Posted by Michael on February 1,2010 | 05:14 PM

    A fascinating story! I can understand why no one was told originally; partially because they were poor black folk and "didn't matter", and another part because it could so become a hot medical/racial issue. I would like to know if the family has been given a 'settlement"
    I will definitely read the book!

    Posted by Nina Knight on February 1,2010 | 05:14 PM

    I think the family should be paid back pay and current since her cells are being sold.

    Posted by joyce ford on February 1,2010 | 05:14 PM

    I too was into Biology and genetics in my early career. My father was used as a guinea pig in many researches done on cancers in the 6o's thru 80's. As long as one realizes there are no color boundaries and that wherever there is a possibility of cultures helping others, money a decrying should not be an issue. Like Henretta's family and my own there was no money forthcoming to family members even though there was that initial resentment

    Posted by gary on February 1,2010 | 05:14 PM

    i was fascinated by the story, well done!

    Posted by on February 1,2010 | 05:15 PM

    This is a very interesting story, yet very sad. The family should have been told and compensated. I was shocked as I have heard of the HeLa cells in school. I can't wait to read the book.

    Posted by Debi on February 1,2010 | 05:15 PM

    I read all of the comments and soon started skipping over any of them that talked about "where is the families money". Those comments showed the essence of ignorance when it comes to medicine and research. First of all, back in the 1950's doctors did not think of getting permission. Secondly, science and research is for benefit of all humans, not a money making scheme for someone or their family, who has a tumor removed. While I agree that what happened was unethical. Those doctors did not make much money on her cells. In fact they probably made VERY little. The pharmaceutical companies, who used the data from research DO make the large sums. But Scientists and Doctors tend not to make much from research.

    Posted by LaFish on February 1,2010 | 05:15 PM

    Wow, nice article, very interesting! My children will be reading this book. Thanks

    Posted by Monia on February 1,2010 | 05:15 PM

    Great article!

    Posted by Mary on February 1,2010 | 05:15 PM

    Beautiful lady and handsome man - must have had beautiful childen and grandkids-very interesting piece

    Posted by yolanda ramos on February 1,2010 | 05:15 PM

    This is great and trully amazing. The family should be compensated. I'll buy the book. Please advise where to get it.

    Posted by Victoria Gonzales on February 1,2010 | 05:16 PM

    Excuse me, but do you have polio? If not, then why don't you write a check to the Lack family yourself? Seems we've all benefitted from this set of cells. All science requires a control group, or a constant. Seems this woman unknowingly became the constant for many things. In my opinion, that doesn't mean her family is entitled to a huge windfall. It's cool for them that she's the one, but honestly, it would have been then next patient if they didn't take hers...

    Posted by Andy D on February 1,2010 | 05:16 PM

    What everyone is overlooking is that these cells are KEYWORD "immortal" which will mean a way to either clone or mass reproduce/rapid regeneration of something and or someone......i predict that zombies will become a reality

    Posted by Reyes on February 1,2010 | 05:16 PM

    I had a similar procedure performed. I better not hear about any AmGo cells out there, LOL!

    Posted by AmGo on February 1,2010 | 05:16 PM

    You can go on Amazon. com and preorder the book. The author couldn't get any publisher to publish this, so she did it herself. the ISBN is 978-1-4000-5217-2.

    and you can read some of the pages of the book on that site

    Posted by Cydney Partridge on February 1,2010 | 05:16 PM

    Wow...interesting article. But why make the brothers look like they were only interested in the money. Heck, they should be; it is their mother. I will definitely check out the book.

    Posted by Zaffa on February 1,2010 | 05:16 PM

    Great story. I always thought that cell normally lived six to seven years and then duplicated themselves and died. Except cancer cells which could be called "immortal" as they duplicate themselves but do not die...They duplicate themselves so much that they form tumors that invade the body.
    Is there a time limit for cancer cells to live?

    Posted by Nicole Meier on February 1,2010 | 05:17 PM

    Beautiful lady and handsome man-what beautiful children and grandchilden they must have had - very interesting article

    Posted by yolanda ramos on February 1,2010 | 05:17 PM

    Amazing story. I think the family should be recompensated, however perhaps she had donated her remains for research. If so, then what she gave the world is beyond any price her family could ask.

    Posted by jim on February 1,2010 | 05:18 PM

    Colleen, You are right, and wrong. Fact is every living thing eventually dies. so you are right.... however, these human cells are reproducing on their own, able to be grown in different laboratories around the world. I would bet that there are more living HeLa cells right now, than what constituted her living body. Think about that for a minute to blow your mind. These cells die off individually, but the strain of cells, from a single human being are going to live indefinitely... that makes them immortal, does it not?

    Posted by Dugan on February 1,2010 | 05:18 PM

    The article was interesting. Not something I'd normally read, but it did sound intriguing. I am definitely going to look this book up the next time I go to the library.

    Posted by Angela Moore on February 1,2010 | 05:18 PM

    Wonderful history. Its great to see how a supposedly routine action by a doctor helped science discover so many other things helpful to the human race through the cells of this amazing woman. God works in misterious ways doesn't he. Nothing is coincidental. Hope her family gets compensated which is the only right thing to do.

    Posted by Eva R. Valdez on February 1,2010 | 05:18 PM

    That story was very interesting. The medical community should be ashamed of making billions off a woman and not attempting to compensate the family.

    Posted by Mike on February 1,2010 | 05:18 PM

    I to was very fasinated by this article. The book can be purchased on amazon right now at a very reasonable price. I already ordered mine. I look forward to finding out more about the incredible-immortal life of Henrietta. And if her family has been compensated, or if the the medical research industry is trying to fight this in court. I have my thoughts in advance that they probably are. But hope they will do the right thing. ahh who am I kidding. ( I dont believe for a minute that they would just turn over money to the family) and maybe the courts should be involved to make sure they are compensated fairly.

    Posted by Betty Neal on February 1,2010 | 05:18 PM

    If the tumor had not been sent "down the hall", it would have been disposed of, probably burned. No one "stole" anything. It was garbage and was useful. With that said, it would seem the family should receive some compensation.

    Posted by Ted Ainsworth on February 1,2010 | 05:19 PM

    A part of Black History

    Posted by Corey Kinlaw on February 1,2010 | 05:19 PM

    A lot of biological researchers do not know about this story, they should read this book so they will care and appreciate more to these cells. Furthermore, they have to be care to her family who live in poverty

    Posted by Subagus Wahyuono on February 1,2010 | 05:19 PM

    What a amazing story. Its very true and real. I like to hear more about it. Only thing the scientists are trying to find the fact or truth, that is sure... beside that what people are saying from different view points, espeacially from religious faith are baseless. Without scientist's help or research done on so many of diseases on this planet there are no any servival from any cureable diseases. So, there is no needed to sue or file lawsuit against the scientist or researchers. You / we all should support and contrubute fund towards them to achieve their successfulness. Then we all gian benefit from them. thanks!!

    Posted by Dell Curry on February 1,2010 | 05:20 PM

    I was taken by this part of the story and had to read all of it. I have only one question? Who and/or How was if verified that Mrs. Lacks did not give the doctor permission to use her cells? Who is a verifiable witness still alive, that was in the room with her and the doctor that day? That's all I'm saying!

    Posted by GD on February 1,2010 | 05:20 PM

    This is a great story! I will buy the book :)

    Posted by T Gregory on February 1,2010 | 05:20 PM

    Really, compesation... restitution. It is a remarkable story but cells come from creation. If you sneezed into a petri dish is that really some sort of effort that requires compensation. Her family should be ashamed for trying to profit off of this other that marketing her biography. They should be thankful that they are a part of modern science.

    Posted by wayne on February 1,2010 | 05:20 PM

    Great story, I would love to read this book. And no matter how good this turned out for science, Doctors did kinda do what they wanted long ago and got away with more than we would like to think.

    Posted by numa on February 1,2010 | 05:20 PM

    Sound like a very interesting story, and I am sure it will sell. Perhaps the 9ollow up book could detail the families pursuit of compensation and the results of that endeavor.

    Posted by Leslie Ann on February 1,2010 | 05:21 PM

    Biological Immortality means "agelessness." The article is wrong, scientists have known for decades that telomerase is responsible for keeping these cells immortal. Most cancers turn off their aging so they can divide forever. This phenomenon is not only restricted to mammalian cancer cells, as many creatures that live in the bottom of the sea (jellyfish, some crustaceans and mollusks) are also biologically immortal. They do not age. Theoretically if predation was removed from the ecosystem these creatures would live forever. Perhaps one day humans will reclaim the curse of immortality.

    Posted by Femto on February 1,2010 | 05:21 PM

    very nice article ! and also a little sad but it is just another example of how blacks have been used and not given any credit for what they have contributed to the world looking forward to reading the book

    Posted by karen on February 1,2010 | 05:21 PM

    This is very interesting.

    Posted by Betty Polk on February 1,2010 | 05:21 PM

    I am absolutely taken by the story and the different parts and sides of it. It totally interests me in so many ways. I would love to share it with others.

    Posted by Shri on February 1,2010 | 05:21 PM

    I love it.. very interesting story . i would love to read this book.

    Posted by D on February 1,2010 | 05:22 PM

    Cells and tissues are generally donated to science. You don't get money for that.

    Posted by Tracy Jane on February 1,2010 | 05:22 PM

    I am not sure that money is a real issue here. I don't think that black or white should be a real issue here. Nothing in the article implies that anyone made "millions of dollars off of this research." That is an assumption of the reader. There are many dedicated researchers in this country that DO NOT make millions of dollars from their research. I think that the real issue here is that future mankind benefited immensly from the research and findings from these unique cells. At the time, in the 1950's, I am not convinced that the researchers knew exactly what they had. I am sure that it took many years to reveal the cell's potentials. also, many of the comments suggested that they are applying today's standards on history. you can't do that! You have to look at what history contributed to the event itself. Yes. There were white black issues. The article does not indicate that there weren't 'white' tissues also collected. I cannot believe that only black tissues were collected. The article has peeked my interest, however, and I will look forward to reading more about the subject. Maybe the book in question, but also other articles out there written about these unique cells.

    Posted by C. Myhre on February 1,2010 | 05:22 PM

    Thank you, I would like to know more, is the book out and where can I by it, and I do think that the family should receive money, because every one will make money on this that is only fair. Marlis Kelleher

    Posted by Marlis Kelleher on February 1,2010 | 05:22 PM

    Is it possible that the Doctor at John Hopkins labled the cells HeLa to hide the fact that they were hervested from a black woman? I say that just thinking of the racial ignorance in those days.

    Posted by Douglas W Richards on February 1,2010 | 05:23 PM

    Perhaps it wasn't just The human cells that were "immortal" but the effect of the type and stage of cancer that caused those cells to become so.

    Posted by mary on February 1,2010 | 05:23 PM

    I am curious that scientists are never stop here. They will try to clone her. And learn more about her personal life. I am sure research never stop here and we will here fifty years from now.

    Posted by hocyrus on February 1,2010 | 05:23 PM

    I think this is a great article. I hope the family was compensated for the amount of education learned and lives saved from HeLa's cells and research. I hope the racial differences can be put to the side and the reality can shine through that MANKIND has Henrietta to thank.

    Posted by Quenton on February 1,2010 | 05:23 PM

    nice article..wow just learn something on black history month...hm wonder did they file a lawsuit?

    Posted by yoyo on February 1,2010 | 05:23 PM

    Amazing, well-told story. Hope to read the book. I don't think the family should receive any compensation; however, I'm do believe people should be informed and have the choice of whether or not they want to donate tissue. My husband is a cancer patient, being treated with an expermental vaccine at Johns Hopkins, and we are greatful everyday for the tissue donors and researachers who are making it possible for him and others to have life and hope.

    Posted by lillian richey on February 1,2010 | 05:23 PM

    What most people don't understand is that whenever you give sample of blood tissue etc. there is a understanding that what you give is possibly going to go through secondary testings and on occasion those test are for some trial they use them for double blinds etc. without cell , tissue and blood samples medicine would be in the dark . And as for the conspiracy theorists, well they have a lot of paranoia and ignorance about science.

    Posted by Donegan on February 1,2010 | 05:23 PM

    sounds nice. Well done

    Posted by RasNaya on February 1,2010 | 05:23 PM

    I'd like to know how Henrietta Lacks' family was compensated for the use of the HeLa cells.

    Posted by Alisa on February 1,2010 | 05:24 PM

    I wonder if the President,s have this information and pass it on to each other during each ones power take over???

    Posted by jon nippa on February 1,2010 | 05:24 PM

    I really enjoyed reading that. Thank you!!!! Sounds like a great book.

    Posted by Casey L. on February 1,2010 | 05:24 PM

    Scientific American published a paper on this subject some 20 years ago. The cross contamination mentioned destroyed several decades of cancer research, all kept quite of course.

    Posted by steve brown on February 1,2010 | 05:24 PM

    This is an outstanding story. What a great way to start Black History month.

    Posted by Denise on February 1,2010 | 05:25 PM

    What is troubling is the fact that scientists from John Hopkins took these cells without requesting permission from the family. Most southern states, Virginia included, were ravaged by violent acts of racism during and prior to the 1950s. There are many stories of scientific experiments performed on blacks without consent nor explanation or reasons. This seems to be just another one of those events where permission was not deemed necessary or needed. Compensation is long overdue!

    Posted by Bruce McLeod on February 1,2010 | 05:25 PM

    Great story...I was a bit disappointed so many people were worried and the $. I am positive this has a happened to many other people. I liked reading the article...wish people would stop concerning themselves with $...

    Posted by E. Imes on February 1,2010 | 05:25 PM

    Congratulations on your perseverence. Wonderful article; wonderful! Normal human cells eventually die through a natural process called "apoptosis" or "programmed" cell death. But this does not happen with cancer cells, which is why, if they are allowed to spread or metastacize, they become so deadly. As long as cancer cells are fed, through the blood supplied by the host or person with the cancer, they will keep on dividing. So they are said to be "immortal." Whether they are, in fact, immortal remains to be seen as "forever" is, indeed, a long long time. Note that I believe that all types of cancer cells (whether from a person afflicted with cervical, lung, liver, prostate etc. cancer are considered to be "immortal." I along with many of the other posters feel strongly that the family should in some way be compensated. God knows that Henrietta Lacks' cells have help so many people. What a great legacy she has left. Whether her family has a legal claim or not, "right is right" and Johns Hopkins, out of gratitude, SHOULD DO SOMETHING! Someone should help the family organize a web site. I unfortunately would be no help in that area. I would make a small donations as I'm sure would many others. What a great story and I'm sure a great book. (if there are words misspelled-sorry but there is no spell check)

    Posted by Dennis Roth on February 1,2010 | 05:25 PM

    WOW!!!!! I enjoyed reading all this stuff. It was so informative and entertaining. I hope Hollywood gets a load of this and decide to make a movie (SyFy)Parts I,II,and III. Pehaps, in that way the family can be compensated for the movie and own the rights. I agree, it's a great way to start off Black History Month!

    Posted by Patricia Spencer on February 1,2010 | 05:26 PM

    It would be interesting to know what disciplines this young persons cells benefited and to what extent. I doubt if an exact monetary value can be placed on exactly how society benefited. Perhaps big pharma might be urged to recompense her heirs with money or jobs. Surely society gained from her time on this planet and her contributions that expanded our storehouse of medical knowledge.

    Posted by edward curry on February 1,2010 | 05:26 PM

    Fantastic research on a very interesting subject, I plan to purchase this book.

    Posted by Lila_Jean on February 1,2010 | 05:26 PM

    wow such a cool story!

    Posted by Naomi on February 1,2010 | 05:26 PM

    GREAT!!!!!

    Posted by Dianna on February 1,2010 | 05:27 PM

    GREAT!!!!!

    Posted by Dianna on February 1,2010 | 05:27 PM

    This is definitely a book on my to-read list. Very interesting article!!!

    Posted by Aleishia on February 1,2010 | 05:27 PM

    I've studied this in my Biology class and I didn't know that her son was homeless. Also, for her family to not have health insurance is just insane. This family didn't know the magnitude of the studies done on her cells, and should be compensated.

    Posted by Tanika on February 1,2010 | 05:27 PM

    very interesting story!

    Posted by Firomsa on February 1,2010 | 05:28 PM

    From Wiki: HeLa cells have an active version of the enzyme telomerase during cell division, which prevents the incremental shortening of telomeres that is implicated in aging and eventual cell death. In this way, HeLa cells circumvent the Hayflick Limit, which is the limited number of cell divisions that most normal cells can later undergo before dying out in cell culture. Wow, that is incredible. Her cells really are immortal.

    Posted by Jessica on February 1,2010 | 05:28 PM

    I used to culture HeLa cells in the laboratory to test proteins that were being developed as biologicals. I didn't know the whole story just that they came from a woman who had cancer. Great information and I will buy the book. Discovery is often serandipitous; most reserachers are after the science not money!

    Posted by Helen on February 1,2010 | 05:28 PM

    This was very interesting. Thanks for sharing.

    Posted by Ty on February 1,2010 | 05:28 PM

    Very informative about something not widely known but very significant. Life transcends all ethnicities and people are more similar than different. My gratitude to the author and Yahoo for the posting!

    Posted by Don Frazier Jr. on February 1,2010 | 05:29 PM

    Very informative about something not widely known but very significant. Life transcends all ethnicities and people are more similar than different. My gratitude to the author and Yahoo for the posting!

    Posted by Don Frazier Jr. on February 1,2010 | 05:29 PM

    these comments about compensation and litigation portray a disturbuing picture of modern society. this attitude to me is disgusting. doesn't the fact that her cells, something so simple which everyone has, performed miraculous things in people's lives make this something to be thankful for? Instead what should be an inspirational story is twisted into being about money, this is just sad.

    Posted by tlmiam on February 1,2010 | 05:30 PM

    An amazing and fascinating story.

    Posted by Nina on February 1,2010 | 05:30 PM

    That's crazy but yeah the family should get paid a lot of money for this becuase the scienist "took some of her cells without her knowing" that does seem like a lawsuit for the poor family!

    Posted by Kat on February 1,2010 | 05:30 PM

    I thought this was a very interesting article except for the inclusion of the thought that the doctors were racists because the origin of the cells was a black woman. I can't understand the mindset that racism has got to be a factor in anything that involves a black person. But these are the times we live in. I do, however, believe the family of the lady should somehow be compensated for these cells that have made untold millions if not billions of dollars for researchers over the years. I'm guessing medical law has not adequately addressed this issue yet, although with the huge amounts of money involved in research discoveries, I'm surprised.

    Posted by Mix Dean on February 1,2010 | 05:31 PM

    that was cool... i want to know more about her... was her daughters' cells wasn't of same kind that of hers...? (curious)

    Posted by ibeth on February 1,2010 | 05:31 PM

    WOW! What an awesome Story! I have so many questions, perhaps I can get the answers if/when I can read the Book! Henrietta Lacks doesn't even know that she has had such an impact on mankind through Medical Research... and it ALL began with HER! How Cool is THAT?

    Posted by Johnny Popp on February 1,2010 | 05:31 PM

    Oh, this cover-up goes deeper. In school, we were taught that her name was Helen Lane, hence the name of the He-La cell line. Until now, I did not know her real name. Why could they have not been more open about this?

    Posted by Gloria Glasgow on February 1,2010 | 05:31 PM

    Well, this has definitely been a trying time for the family. We can all speculate, however I hope even after the money hungry issues that this family get what is rightfully theirs; that they have a good attorney with their best interest at heart and no grudges are held. I am looking forward to reading the book. We will not forget the past, but well will not allow it to rob us of our future!!!

    Posted by Celeste Graham on February 1,2010 | 05:31 PM

    this is an amazing story. I found a good book to pick up and the story itself is a lesson learned....People are so blind-sided with medicine these days.....

    Posted by Brandye on February 1,2010 | 05:31 PM

    What a very touching story. It shows that we never truly die, just transform to something else. I will buy the book.

    Posted by Vicki on February 1,2010 | 05:31 PM

    Interesting...I've never heard anything like it.

    Posted by Janay on February 1,2010 | 05:31 PM

    Whaaat..!!, Now if this woman is watching this from somewhere won't u scientists get in trouble?! Try exchanging my cells for prices sometime when u'll not be seeing me around and look at what will happen to your foreheads! Anyway just want to say, whoever is in busin ess...Buying, selling these cells please remember she left family...hope u get me. Thanks to the writer.

    Posted by Deus on February 1,2010 | 05:32 PM

    A fascinating article. It really brings to light many issues dealing with medical ethics, as well as underscoring the contributions of many unknown or unsung persons (of any race). I am certain Henrietta Lacks would be proud of her contribution to the betterment of all mankind, and that her family, particularly her daughter, can know that Henrietta Lacks, and not just her cells, will be "immortal".

    Posted by Glenn on February 1,2010 | 05:32 PM

    I found this story to be very interesting. This is something that should be on 60 Minutes. I would like to see what they would do with this information.

    Posted by Paula on February 1,2010 | 05:32 PM

    Amazing indeed! Henrietta didn't realize what a remarkable contribution to mankind she made. It is too bad that such a poor family could not have been compensated for these cells that have helped humanity up until today and many decades from now. Our world owes Henrietta the world. Instead she didn't receive anything for her contribution. Someday, our world should give back to her family so that they can benefit somehow, too.

    Posted by Fay Kirkopulos on February 1,2010 | 05:32 PM

    This ssound quite interesting! i've been captivated by it

    Posted by Me on February 1,2010 | 05:34 PM

    absolutely amazing!!! i cant wait to read the book and get more in depth on this!!!

    Posted by tammy on February 1,2010 | 05:34 PM

    Fascinating story

    Posted by lucy on February 1,2010 | 05:35 PM

    That is amazing ,I'm very interested in knowing more. Very nice piece on HeLa cells

    Posted by on February 1,2010 | 05:35 PM

    While i was reading this i thought NO POSSIBLE WAY!!!!!!!! But when was the last time scientist lied to us

    A: ALWAYS

    Posted by Peter on February 1,2010 | 05:35 PM

    Sounds to me like a bunch of money grabbing people that wants to make a buck off this woman.

    Posted by on February 1,2010 | 05:35 PM

    Fascinating!

    It also means that the stem line is 88 years old when accounting for her age in 1951. Such a fascinating thing and now i want to read the book.

    Posted by KristinaM on February 1,2010 | 05:35 PM

    GOOD! THE TRUTH ABOUT WHO "INTRODUCED" HIV INTO HUMAN BODIES SHALL BE REVEALED SOMEDAY!

    Posted by WOLE on February 1,2010 | 05:35 PM

    Whaaat..!!, Now if this woman is watching this from somewhere won't u scientists get in trouble?! Try exchanging my cells for prices sometime when u'll not be seeing me around and look at what will happen to your foreheads! Anyway just want to say, whoever is in busin ess...Buying, selling these cells please remember she left family...hope u get me. Thanks to the writer.

    Posted by Deus on February 1,2010 | 05:35 PM

    POWERFUL, NOTHING CAN COMPARE TO THE HUMAN'S CREATION. THIS STORY IS BREATHTAKING, The family should be amazed that their legacy of genetic's is unheard of.. If I were one of them I would be so proud to know that my mother may have contributed to history and science in some way... and that God created my mother unique from anyone else... the family should not be concerned or worry about money,, God will surely bless them,, he already has,, by their mother be so unique in her creation,, her cells will live on...

    Posted by Thresa Graham on February 1,2010 | 05:35 PM

    This story is sad and happy Sad in the sense that a hospital such as John Hopkins would even think of doing something like this. Did the doctor figure because she is black and poor we can just experiment on her and not tell the family about it. And even though there were many breakthroughs in medicine because of this.it's the way it was done thats just like a slap in the face to many african americans.It makes me wonder how many other stories are out there like this one hidden away in some lab. At the very least the Lacks family should get a formal apology and full compensation from the hospital for such a cruel act.

    Posted by royalfuzziness on February 1,2010 | 05:35 PM

    This story is fascinating,the end-result might have been good,but i agree with some of your readers.The initial morale of taking this poor woman'cells without her knowledge constitute a sin in itself.

    Posted by nekens colin on February 1,2010 | 05:35 PM

    I'm sure Oprah would love to read your book and do a show about it! Thanks for bringing the story to life. Henrietta deserves it!

    Posted by Sheila on February 1,2010 | 05:36 PM

    This is intriguing. It is nice to see history from a woman’s plight.

    Posted by Laurie on February 1,2010 | 05:36 PM

    very interesting story to share and thanks to HeLa though she did not know about it... scientist can't explain why the cells are still living and cure diseases so i can conclude that there's GOD that scientist never believe..

    Posted by anecita resos on February 1,2010 | 05:36 PM

    The doctor did not have any right to take cells from this woman without her permission. The brothers sound like a bunch of money hungry jerks!

    Posted by Susan on February 1,2010 | 05:37 PM

    A wonderful piece of history well told. I look forward to the book. I have no right to judge whether any family related to cell cultures are due remuneration. I would freely donate my own cells for culture if it would help someone. Yes, scientists would charge for them as they have time and money involved in preserving and culturing them,etc. What I really would not agree with is some big corporation copyrighting someone's cells and then restricting that person's right to donate as they see fit. I know that is a science fiction idea, but a lot of things we have today were first thought of by science fiction writers.

    Posted by Mary McCue on February 1,2010 | 05:37 PM

    I will read the book sounds interesting my older sister died from ovarian cancer 3 years ago she wouldve been 39 this year.

    Posted by Hazel king on February 1,2010 | 05:37 PM

    I am a nurse and found this article especially provocative, it informs the need for research involving the use of human cells and the benefit to mankind. The article also chronicles the progressive recognition of the medical-legal issues involved in scientific research and the development of ethics in this area over time. Most interesting to me is the validity of the inspiration of young students and how these young people can ultimately inspire the general public because of their investicatory discipline and tenacity. Ms. Skloot demonstrates why we all should be aware of young people who could benefit from our attention and mentoring. I am committed to reading her book and recommitted to searching out youngsters in my community who might benefit from interaction with a mentor.

    Posted by Patricia on February 1,2010 | 05:37 PM

    Amazing story. Definitely interested in reading the whole story.

    Posted by Glynis on February 1,2010 | 05:38 PM

    So, what I take from this is that her *cancerous* cells refused to die. So, does this mean that the "fountain of youth" exists, but is actually tied to cancer which destroys the host but then can go on to live forever itself? Have other cancer cells also lived on seemingly "forever"?

    Posted by chloesmom on February 1,2010 | 05:38 PM

    The majority of information about our world is not exposed. I feel the book is very good and helps everyones awareness. More power to open information.

    Posted by Don Morgan on February 1,2010 | 05:38 PM

    A very interesting story, all together. I feel bad for the family, because it must have come as a bit of a shock, but I think the scientists should have been disciplined in some way for selling the cells without giving the family at least some of the profit. Serves them right I say.

    Posted by Tara on February 1,2010 | 05:38 PM

    Yes the family should be compensated didn't other's that weren't family gain money from her.Better family than outsiders.

    Posted by kim on February 1,2010 | 05:39 PM

    People see sinister deeds behind every scientific effort. Add the stupidity of racism and you get a good story. The white man stealing a dying black womens cells to profit off of. The white women taking the story and selling a book. How about the brothers not caring till money was at stake. Big Pharma using the law to develop huge profits off of one dying persons cells. This story is not full of villians: a innocent dying women getting treated and a scientist finding cells that can be replicated and grown for multiple uses for scientific advancement. If it was not her cells it would of been someone elses sooner rather than later. To me it provides a great opportunity for black americans and her family to be proud of something they contributed to for all mankind, not a whitey done me wrong story like some of the posters here state... To me this contribution to mankind is something bigger than a few hundred dollars someone might of received for authorising the use of their cells in the 1950's.

    Posted by Blue Eyed Devil on February 1,2010 | 05:39 PM

    I got a degree in biochemistry and ethics classes were required for this major. So much of our understanding from gene mapping to developement of vaccines comes from this WOMAN. Michael Herring posted that this family isn't entitled to a bunch of cash and that those who donate their bodies have also contributed to science w/out any expectations. Well guess what her cells have contributed greatly (more so than any it appears) and it certainly didn't sound as if she donated her body or even gave consent to have a tissue sample taken and used. I'm also willing to bet that Darna Young, who also posted a response, was right about this woman probably not getting any treatment and dying months later. I believe this woman's family should get some compensation or a at least a foundation, as Richard posted, should be set in place for the Lacks Family.

    Posted by csmathews on February 1,2010 | 05:40 PM

    I learned about HeLa cells in an anatomy class I took in the late 70s. We were discussing cell differentiation and how these cells could be manipulatedfor various purposes. Interstingly He La was identiified as Helen Lane. I will read the book

    Posted by Harold K on February 1,2010 | 05:40 PM

    I'm on the waiting list at my neighborhood library and look forward to reading this beautifully written book. Henrietta and her husband make a srickingly attractive, prosperous looking couple. I hope her family realizes how profound her contribution has been and apparently continues to be for all of us. How wonderful to know about her the first day of Black History Month.

    Posted by Patricia Fairfax on February 1,2010 | 05:40 PM

    We now know that cervical cancer is due to an infection by the Human Papilloma virus. Maybe it was the virus' genes that incorporated into her cell's DNA that made it "immortal". Maybe the immortal cell line created was actually a clone of the cancer cells and not of the normal human cells from HeLa .

    Posted by Si Nguyen on February 1,2010 | 05:41 PM

    What a fascinating story! I can't wait to read the book!

    Posted by Sylvia on February 1,2010 | 05:41 PM

    This is a great story; why now we needed to know this years ago for Black history. I would hope Henrietta Lacks family was compensated; this lady contribute to moderates science her cell contribution help to making "Polio Vaccine" now the great thanks for the information.

    Posted by Carolyn Morris on February 1,2010 | 05:41 PM

    yea right, Nice piece alright. But those that have been profiting from them womans tissue over the years should go package like $1billion and give to her family. Her family should also get themselves a good lawyer and get to work suing them companies for a piece of the action. what is good for the goose ought to be good for the gander if you know what i mean.

    Posted by john okonkwo on February 1,2010 | 05:41 PM

    wow...very interesting story,how come all these years i never heard of HeLa Cell??i am very interested and will want to know more.pretty amazing piece of information

    Posted by tese on February 1,2010 | 05:41 PM

    If the original cells were cancerous tumor cells, wouldn't the cells that are growing from the original sample be cancer cells? If that is the case wouldn't all the research being done be on cancer cells, and how accurate is that? Is that explained in the book?

    Posted by mar on February 1,2010 | 05:41 PM

    This is confirmation. When I was little my mom told me of this story, since I lived near John Hopkins Hospital. She also explained that cloning and testing was being done on people who disappeared over a weekend in the area of the hospital. Somehow, this family even uneducated had enough sense to know that they should have had more control over the tests and decisions that were being done to their dearly departed mother. Word to the wise...stay involved with every part of the diagnosis, presciptive and future plans of whatever experimentation....Above all...GET THE MONEY if people are getting paid for any of your bodily parts!

    Posted by Tine Green on February 1,2010 | 05:42 PM

    I would buy this book great work!

    Posted by Morris Williams on February 1,2010 | 05:42 PM

    What a story, It catches your attention from the very start. It made me angry, than it made me happy, You never know what some doctors will do, and never say a word, trust sometimes goes out of the window with some people. I would love this book where can I get it. God bless you who searched for the truth.

    Posted by Laur Derozan on February 1,2010 | 05:42 PM

    Such an interesting article-I would like to read this book. But why does money have to even enter the conversation? Science is about research-and we all contribute to research when we donate blood,have tissue removed (like a gall bladder) or have any operation. Greedy!

    Posted by Laurie G on February 1,2010 | 05:42 PM

    Reminds me of what they did to the Tuskeegee airmen, doing unwanted and dangerous test on those men without their knowledge... Ain't no telling what they did to that poor woman????

    Posted by Juanwesley on February 1,2010 | 05:42 PM

    Reminds me of what they did to the Tuskeegee airmen, doing unwanted and dangerous test on those men without their knowledge... Ain't no telling what they did to that poor woman????

    Posted by Juanwesley on February 1,2010 | 05:42 PM

    Great article! I must buy this book!

    Posted by latanya on February 1,2010 | 05:42 PM

    Very interesting piece. I figured that before I got to the end of it the family would want some MONEY from it.

    Posted by John P. Pollard on February 1,2010 | 05:43 PM

    THAT IS THE COOLEST STORY EVER!!!!!

    Posted by nobody on February 1,2010 | 05:43 PM

    Dr. Alex Carrel in 1912 was awarded with a Nobel Price in Medicine..he wrote and said... "The cell is inmortal ... If our cells are cleansed of all toxins and the proper nutrients are provided, as far as we know, the pulse of life may go forever." So what's the big deal now, about the inmortality of the cell. Science has known that all along. They haven't said it or taught that, that's a different story. The question here is, why the establishment did not want the regular people know this and myriads of other things? Good question.

    Posted by Bert Chadwick on February 1,2010 | 05:43 PM

    darwin teaches ? his works read like h. g. wells but not near as good. these hard working people gave while they lived and years after they died. where is the movie.

    Posted by rick v. on February 1,2010 | 05:43 PM

    WOW,WHAT A STORY.I WAS SO WANTING TO HEAR MORE,AND ALSO CURIOUS ABOUT THE FAMILY BEING COMPENSATED. I TO AM FROM AN ANCESTRY OF SLAVES, SO I WOULD LIKE TO KNOW IF ANY OF OUR CELLS WOULD BE BENEFICIAL TO RESEARCHERS. JUST A THOUGHT ANYHO CUDOS TO YOUR STORY.

    Posted by Renie on February 1,2010 | 05:43 PM

    fascinating article, it is very informative for I had not heard of Hela cells. But again it does give creedance to the fact of how what ever wrong White America does or has done to African Americans, its always trivialized. Some of the comments from the readers of the artical act as though they didnot understand what they read. The cells were taken without her knowledge. Yes, it has helped many people, but the money realized from this venture reaches astronomical proportions and her family needs to be compensated. I can't believe anyone feels the it was alright to do what was done. Again, it shows that white America has no respect for our dignity as human beings. Its still business as usual.

    Posted by Constant Serrette on February 1,2010 | 05:44 PM

    What? Where is Henrietta now?

    Posted by Bubba Heff on February 1,2010 | 05:44 PM

    WOW!!!What a great discovery. I think this is the generation of people who can live forever if they want to. Those cells, if it is true, can regenerate any part of your body to replace your rotten parts so there's even no fear of getting sick because all your parts can be replaced with a good cell. What is amazing with Henrietta is her cells are just the very few that stayed alive to this day. This is a wonderful phenomenon. Hey, I think I want to live forever now or until I get tired of living or drop dead, if it is at all possible, because I want to do a lot of things for humanity. This is a very exciting world. I want to live forever like Henrietta? Can these scientist revive her or clone her? What's in her cells that made it more durable than the rest of humanity? I want to know and I want to read the book.

    Posted by Cherry Dizon on February 1,2010 | 05:44 PM

    If everyone just stoped for a moment and realized underneath that thin layer of skin everyone in the wold is the same, we might start to get along with one and another. God Bless!!! Bob 2-1-204:44pm

    Posted by BOB on February 1,2010 | 05:44 PM

    Hat's off and a standing ovation to the writer, Rebecca Skloot, what an awesome discovery and captivating truth.

    Posted by Jean Keys on February 1,2010 | 05:44 PM

    I am so interested in this story, I must have this book. Thank you for sharing...

    Posted by Kat on February 1,2010 | 05:44 PM

    This is a very interesting piece. I do believe though that the family should be compensated for what was taken from her without her and her family knowledge. I'm glad the writer brought this out in the open how the blacks were taken advantage because they had no education. Why the scientist just didn't ask for her cells, then it wouldn't have been such a secret and the family would not be going through what they are going through now. Yes, cells are important to science but I think the scientist should be more open to what they do behind closed doors. We the people still don't understand where AIDS came from (no direct answer). Yes, people have donated their bodies but they have to sign the back of their license to do so with out that signture they would have to go through the next of kin. Will read the book.

    Posted by Annette M. Redd on February 1,2010 | 05:45 PM

    Interesting and informative to think that a doctor in the 1950's was thinking outside of the box to use Henrietta Lacks' tissue to use in research. Her life has truely made a difference to humanity. Thanks to the teacher who sparked a student's interest in researching the story is a true testament to good teachers iand education. I intend to read more about Mrs. Lacks.

    Posted by Lizzy43 on February 1,2010 | 05:45 PM

    It's a compelling narrative, however even though I took an intense biology lab course in college most of the scientific jargon and analysis was confusing, at best to me. I do know that the basis of cancer is cell division, multiplication that won't stop. Isn't that why her cells are immortal. Or is it something peculiar to her geneology, or the fact that they are cervical cells - the organ that spawns new life, at the center of this debate.

    Posted by reba on February 1,2010 | 05:45 PM

    Interesting...if it was a white family, they would be rich by now. I encourage the family of H.L. to sue the heck of these people who had the nerve to steal cells, make their millions, and we are still poor, out on the streets and no one cares that our cells developed all these vaccines, etc. to help other people who also paid for the shots, etc. It wasn't and will not be "free".

    Posted by deeceetso on February 1,2010 | 05:45 PM

    We're all a source of data for someone's experiment. What I've gleaned from this and other inputs is that morals are imposed much more readily in today’s world than was applied for any of us living through days with so much less transparency.

    Posted by Joseph on February 1,2010 | 05:45 PM

    Great story, the book should be great, I wouldnt be opposed to a trust being established for the family.

    Posted by Brent on February 1,2010 | 05:46 PM

    Really interesting this can change a lot of enigmas of health science, medicine even just simply the life, amazing

    Posted by Roberto Arauz on February 1,2010 | 05:47 PM

    It's very strange to me that even other comments on here (quite possibly from either poor and or uneducated individuals) also seem to agree that 'someone' "OWES" her family 'a lot of money.' For what? Because some intelligent scientist and or doc took a few cells from her tumor? To help aid in the possible discovery of something (and fortunately it has!) to help other human beings on this planet. It has nothing to do with race but I'm also quite certain so many knuckleheads out there in American La La Land will also believe that has or had something to do with it. Get a life and why don't you complaining fools who think everyone owes someone something monetary come up with something to help our fellow beings on this planet?

    Posted by John P. Pollard on February 1,2010 | 05:47 PM

    Wow!! I think I've heard parts of this story before but this is the first time I've learned all the details. Having depression era parents who had parents born around the turn of the century, there was always a fear of mainstream white medicine. Black people knew that white medical doctors sought them out when they were sick, near death or dead to do testing. The horror and stigma of that time remains as can be witnessed in the HeLa Cell story. I anticipate that this book will be a catalyst toward healing the stigma and restore trust in white mainstream research and medical practices. What a great story for the Washington Post to choose to kick-off Black History Month.

    Posted by Nude Provocateuse on February 1,2010 | 05:47 PM

    Horrible....and interesting. This doctor took cells without Henrietta's consent and experimented on the them. This all led to a multi-billion dollar industry of which the family reaped no benefits. Its not right. Another black family robbed!

    Posted by Sonja on February 1,2010 | 05:47 PM

    this is my great great great great aunt! this is pretty cool, my dad is named after her husband and son.

    Posted by Lyinda Lacks on February 1,2010 | 05:47 PM

    Great story! Well written. I want more. All the effort and research will be greatly appreciated when I get my hands on that book!

    Posted by Keshia Kola on February 1,2010 | 05:48 PM

    Very interesting story, don't these people know we all started out from Adam and Eve, maybe black maybe white !
    If her tissue helped people isn't that wonderful, lets not be greedy. Thanks for the story !

    Posted by MArilyn Catt on February 1,2010 | 05:48 PM

    If we took this story back to 1950 it would be a black and white story. Think about it this story and the cell regeneration is still going on in today's society.This is not a race story it's about greed and not giving what's righteously deserve. Too scientist it's about a cure true it might be but you can't go robbing people.

    Posted by Lakeva Crim on February 1,2010 | 05:49 PM

    Why does it always have to be about money, you morons? No one owes ANYone anything. She is dead and good came from the research, why can that never be enough? He family didn't do squat. Why should they get money?

    Posted by notastupidliberal on February 1,2010 | 05:49 PM

    Just think she nor her family have been compensated. The theft, the Doctor stole form her, covered it up with false name, made research history, made money, contaminate and produced only God knows what. This is the same old story of "Big Fish Eats Little Fish." Never giving the little fish a chance to become a medium fish. In 1950 becoming a big fish for some races is out of the question. Now you know there is also another side to this story. The doctor didn't realize that what he was doing was stilling but only wanted to do research on the cancer cells. But discovered something fascinating.

    Posted by Thompson on February 1,2010 | 05:49 PM

    Why does everything have to do with money? You think this lady's family should get paid millions of dollars beacuse she has cells that dont die. Sort of sad that everyone wants to get paid for helping out there own kind. But, very interseting story just dont think we need to get lawyers and other greedy people involved and Thanks Henrietta

    Posted by Peter on February 1,2010 | 05:49 PM

    This reminded me of Ecclesiastes 3:11 "Everything he has made pretty in its time. Even time indefinite he has put in their heart, that mankind may never find out the work that the true god has made from the start to the finish" meaning that in the begining we were created to live for ever, if you doubt this, tell me the (date) that you wish to die.

    Posted by antonio on February 1,2010 | 05:49 PM

    This is really something. I would love to read the book.It just goes to show how one life can mean so much to so many. She is a big part of history.Her family should be so proud.

    Posted by karen on February 1,2010 | 05:50 PM

    I find this article so just amazing. I would love to read the book. I am sad that it has taken so long for us to learn about this contribution to the medical world.

    Posted by rjcarter on February 1,2010 | 05:50 PM

    This is so fascinating and eminently relevant. If I read the article correctly the author is not criticizing medical and scientific research methods but rather asking the question how do we ensure basic human rights and give a voice to the voiceless. It sounds like Henrietta has unknowingly helped and even saved millions of people, but she was not given a say in whether a part of her was used to do so. Can science use the individual to help humanity without respect for the individual’s choice? I can’t think of anymore important question that needs to be answered.

    It is so refreshing to read something other than tabloid trash or sensationalized news. I look forward to reading the book! Thanks.

    Posted by Alan Bar on February 1,2010 | 05:50 PM

    Intresting story it was a good read. It's ashame that the family only see a pay check for somthing they had nothing to do with. I don't care if it was a relitive they are not tilted to any compensation it did not affect them or the out come in any way. Their mother would still have died before her time. Why can't the family just be happy that their loved one helped save millions of people and will continue to serve the grater good of man kind. Monetary compensation should not have even been on their minds. This tells me what kind of greedy people this family realy is. I hope that they dont try to sue it would a sad and i can't believe that racist white scientist even came up that could start a whole nother conversation.SELFISH

    Posted by Martin on February 1,2010 | 05:51 PM

    next time the doctor orders a biopsy on you,tell him you will sell it to him,see how that goes.maybe we can offset dr bills by selling blood samples taken to save our lives.

    Posted by bob on February 1,2010 | 05:51 PM

    Now, what I like to know, was her family ever given in financial compensation? If this was done how much more is not being said about other human beings tissue stealing ?

    Posted by Brenda on February 1,2010 | 05:51 PM

    If they injected her DNA into an egg cell and fertilized it there would be another family member. This case is going to be precidence-setting case for decades and centuries yet to come. Do you own your own genetic code, or can it become public domain?

    Posted by Jim Tsutsui Jr. on February 1,2010 | 05:51 PM

    I wonder if the family ever got money from this I'm sure someone got rich off it they should have got a cut!

    Posted by Lee on February 1,2010 | 05:51 PM

    It is a wonderful story. I enoyed readind both the articel and the comments.

    Posted by Simeneh on February 1,2010 | 05:51 PM

    I hope that Family lives a Happy Rich Life. Their mother saved millions, now it is time to help out that family.

    Posted by Steven on February 1,2010 | 05:51 PM

    What a wonderful gift of information Ms. Skloot gave this family! It is absolutely horrific to think, despite the landmark benefits to humankind, how scientists could take this woman's cells, unbeknownst to her family, and use them for any kind of research purpose! I know that by today's standards, this would not be legal; but I also know that it is probably still done. I would not like to think that my cells were kept alive immortally for any reason without my approval. And I would not give approval. I sincerely hope that the corporation who has profitted so greatly has suitably reimbursed this family.

    Posted by HF on February 1,2010 | 05:51 PM

    My heart leaped when I read the intro. I thought, finally we all see infiniteness of breath of life, that is all around, life being manifested. It is us. Anxious to read more from the book. I honor the worker who presented this gift to humankind.

    Posted by juanita t on February 1,2010 | 05:52 PM

    Very interesting! Why does everyone think that her family is owed something? If that is all you have gotten out of this story then just turn off your computer now.

    Posted by Thomas on February 1,2010 | 05:52 PM

    A must read book. As a Nurse in the area of cellular therapies, this book tells the story from a different angle.

    Posted by Joaquin on February 1,2010 | 05:52 PM

    great article......but instead of saying black you should say African-American :) thanx

    Posted by Stacy on February 1,2010 | 05:52 PM

    what is it??

    Posted by cathy on February 1,2010 | 05:53 PM

    What an awesome story. It doesn't seems amazing that human cells made in the image of God would not be able to live eternally. But it does seem amazing man's abilty to be so conniving and deceitful. Well, the Bible does tell me this also, so I should not be surprised. I hope the descendants of Henrietta Lack were compensated for the use of their loved one cells. But I know no amount of money will every replace that loved one. I appreciate your tenacity to pursue this story and bring it to the light of all people, all races, and all human beings. It explains both our frailities and our resilence. We are weak( as humans) but are cells are strong (as biological elements).
    God Bless You.

    Posted by servant on February 1,2010 | 05:53 PM

    Why has all this very important information been hidden. What a wonderful story. This is truly history. I can't wait to read this book.

    Posted by Betty Mason on February 1,2010 | 05:53 PM

    Thank you! Henrietta Lacks and your family.

    Posted by karen on February 1,2010 | 05:53 PM

    Thank you! Henrietta Lacks and your family.

    Posted by karen on February 1,2010 | 05:53 PM

    http://rebeccaskloot.com/ The book and info on the author.

    Posted by George on February 1,2010 | 05:53 PM

    See Wiki saids
    http://en.wikipedia.org/wiki/Henrietta_Lacks
    "
    In 1996 Morehouse College in Atlanta, Georgia, and the mayor of Atlanta recognized the late Henrietta Lacks' family for her posthumous contributions[9]. Her life was commemorated annually by Turners Station residents for a few years after Morehouse's commemoration.[10]. A Congressional resolution in her honor was presented by Robert Ehrlich following soon after the first commemoration of her, her family, and her contributions to science in Turners Station. [11]

    In 1998, "Modern Times: The Way of All Flesh", a documentary on Mrs. Lacks and HeLa directed by Adam Curtis, won the Best Science and Nature Documentary at the San Francisco International Film Festival.
    "
    So ??????????????????????????????????

    Posted by Joe Li on February 1,2010 | 05:53 PM

    So did the family get any money???

    Posted by chad on February 1,2010 | 05:53 PM

    God bless you my sister! This is a very interesting and informative story. It is not always about the money! Yes! I agree that the family should have been notified. However, now that this happened! Lets save some lives! Continue the research and let Henrietta Lacks rest in peace! Maybe someone will make a movie! I will read the book!

    Posted by Theresa on February 1,2010 | 05:54 PM

    This is a very interesting story, as is the many varied comments on it. My thanks to all the characters that played a part in the creation of the story. Starting with Mrs. Lacks and the doctor. The fact that he took her cells without asking her are telling her family what he had done was wrong and very disrespectful in my opinion. Yet many people have medically and financally benefited from his action. Therefore, I believe anyone who gains financally from this story or the use of HaLa Cells should share those proceeds with her family. My deepest symphathy to the Lacks Family in the lost of their loved one.

    Posted by Barbara on February 1,2010 | 05:55 PM

    This is an amazing story about a black woman, health and the American society/history. Even in medicine there was no such thing as equal rights. I hope the family is being compensated for the acts of those medical "professionals". Sounds like malpractice....was that around then? hmm...

    Posted by Dayna on February 1,2010 | 05:55 PM

    I noticed at least one person, Colleen, mentioned that the cells will eventually die. This is not true, they are actually immortal. As long as the cells are properly taken care off they can technically continue forever. This is because they are a kind of cancer cell with an active telomerase enzyme, telomerase enzymes prevent telomeres from shortening during replication. Cancer cells, can circumvent programmed cell death so they will not die that way and the telomerase ensures the DNA never shortens (IE runs out). So, yes this are actual immortal cells. Someone also mention that they did not think the family should be compensated. Because people who donate their bodies are not. The big thing there is they donated them. Ie gave them up. This woman quite literal had her cells stolen.

    Posted by on February 1,2010 | 05:55 PM

    As a biology student who has extensively studied cells in class and has used various cell lines in conducting research, I can say that the term immortal is more in reference to the line of cells and not the cells themselves. The author isn't saying that the cells don't die, just that they can reproduce infinitely. This is why they are so helpful in research. You can visualize the results for generations. All cancer cells are immortal, because that's what cancer is: the explosive, unrestrained reproduction of cells. I'm not sure how I feel about the compensation part of the story, but there's a book by Michael Crichton, "Next", which deals with a scenario similar to this.

    Posted by Brittany Smith on February 1,2010 | 05:55 PM

    This woman's cells have been a great contribution to medical science. I think her decendents should be rewarded. And she should be enscribed into medical history. Hosea

    Posted by Hosea Morrow on February 1,2010 | 05:56 PM

    I must say that this was a very interesting story and I hope that Mrs.Lacks family is very proud of this and understands how they as a family have made history and helped save the lives of millions of people. We all know that Millions of dollars were made off of the "HeLa" cells and obviously because of those cells millions of lives were saved So, why not give back to the family of the Lady whom has given so much to mankind? It's only right and I hope that the Lacks family has recieved some type of compensation because science has been using them for years and for good things so why not give back to the family that provided you with the means to save more lives..? Great article and a true eye opener!

    Posted by CoCo on February 1,2010 | 05:56 PM

    Quite a fascinating story, who knows what the mad scientist do, and experiment with, who knows what they are doing out there with our cells they collect with out our permission or knowledge. I feel that the Lack Family should be receiving some kind of a royalty from it, after all who knows what goes on behind closed doors, in labs!!! The Lack Family should know what is Happening and going on!!!

    Posted by Izybee walla - sacto. ca. on February 1,2010 | 05:56 PM

    wonderful data, worthy of admiration

    Posted by Cesar Corporan on February 1,2010 | 05:56 PM

    WOW!!!!!!!!!! I want to buy the BOOK.

    Posted by beck on February 1,2010 | 05:57 PM

    has anyone ever considered that by promoting and growing her cells and keeping them alive and using them in vaccines that we've carried her cancer cells right along with them? Possibly giving millions of other women Cervical cancer?

    Posted by Mary on February 1,2010 | 05:57 PM

    I just split a flask of Henrietta's cells about an hour ago!

    Posted by Jake on February 1,2010 | 05:57 PM

    Its obvious that most of these comments are simply from a bunch of folks lined up to pose as independent persons. Based on similarities in the comments, there is a conspiracy to create a sense that, it was done without harm to anyone. These folks were taken advantage of, if you ask me.

    Posted by Maxxy on February 1,2010 | 05:57 PM

    I love it. I think there should be a movie about this. for all to learn.

    Posted by Mario T. on February 1,2010 | 05:58 PM

    i think this article is amazing. I did not know that they could clone from cells taken 25 years ago . Things like this are crazy sometimes I wonder if i was cloned.

    Posted by lori on February 1,2010 | 05:58 PM

    Thank you Henrietta. I was vaccinated for polio when I was a child. I had polio.

    Posted by Donald on February 1,2010 | 05:58 PM

    this is so fascinating! especially to me, my brother is a cancer survivor. i would love to read the book!

    Posted by GraceVT on February 1,2010 | 05:58 PM

    Wow!!
    I am speechless this one should be a movie... hello Hollywood.

    Mrs. Henrietta Lacks was a beautiful lady.

    Posted by Helen Caston on February 1,2010 | 05:58 PM

    First off..the cells tested on were cancer cells from her removed malignancy. Second..There was no standard or rules or laws back then on experimenting on ones cells once removed from the body, black, white or asian. Third..If she was indeed a poor farmer, then she did not have the money to pay for the treatment of her cancer, and removal of tumor and the use of her cells in research were used in leiu of payment.

    Posted by kf on February 1,2010 | 05:58 PM

    Fascinating!

    Posted by Jack Kent Cooke on February 1,2010 | 05:58 PM

    Michael, I do not see any logic behind your statement. It clearly stated that the cells were involuntarily removed without her permission. Yet you say little to no compensation is required? I would say that's a criminal offense and that they are entitled to quite a bit of money. Would you say it's ok to take someone's kidney without their permission to give to someone else in need? It may seem like a morally correct decision, but a criminal offense nonetheless.

    Posted by Ryan on February 1,2010 | 05:58 PM

    I have a question, did they know that the so called "Immortal" cells are not that typical cells that we know of? I don't know, I just research and discovered something that it has something common with a cell that has found from a meteorite. I don't know what that is, but I'll find out about that... Is it possible that people would be "Superman" like or "Godlike". If so, then I would really find out how...

    Posted by Dwaine on February 1,2010 | 05:58 PM

    not complete story .....lots of questions left behind.....
    need complete details to satisfy the readers...

    Posted by mila on February 1,2010 | 05:58 PM

    hi i am 13 years old.i enjoyed this biography.i will like to know more.

    Posted by Malik on February 1,2010 | 05:59 PM

    To C. Frazier-
    Anyone can sue anyone for anything at any time. Whether or not they would win is another story. I'm guessing they would not because at the time, there were no laws against what the doctor did, especially if you consider the fact that she was African American and a woman. (This is 1951 we're talking about.)

    Posted by Cavelka Gorkenfilg on February 1,2010 | 05:59 PM

    I WONDER,,DID THEY DO THAT TO THE 7 POUND TUMOR THEY REMOVED FROM ME..MAYBE IT IS STILL LIVING...I NEED TO ASK MY DOCTOR...I hope more and more is reveal to get an in the natural for HEALING OF MANY BODIES...THAT SOUNDS GOOD TO ME

    Posted by YVONNE PRIESTER on February 1,2010 | 05:59 PM

    Someone does something for the betterment of mankind and automatically someone wants bucks wow we have certainly reached bottom of the barrel.Tumors are a foreign object to someone and thrown away daily in operating rooms. But lawyers want to make a buck God our society is sick.

    Posted by Ron Bigbee on February 1,2010 | 05:59 PM

    This is a movie story...

    Posted by on February 1,2010 | 06:00 PM

    fascinating story. BEWARE:On most hospital admission forms it generaly has a small section about keeping specimens or something similar to that language, people don't generaly read everything that they are signing. For example I had a still born baby midway through my pregnancy, the fetus became the property of the hospital to do whatever with (didn't realize at the time to devestated) it probably was used for medical training or research. Also when you have a baby if you do not designate were your cord blood will go they keep it ($$$$$big buisness). If you don't keep it yourself you should probably donate it, cord blood is amazing.

    Posted by Annie on February 1,2010 | 06:00 PM

    Just to know that after so many years her death, Her cell shows a great sign of hope in the problems we are facing with health today.i feel the story has it's up's and downs, and most of all it's a strong controbution to a healther lives.

    Posted by showhon on February 1,2010 | 06:00 PM

    This was an extemely facinating story. Kudos to the author for following through with your research to accomplish such a feat. I strongly agree with few of the above comments in that the Lacks family is definitely due financial payment of some kind. The world has benefited greatly from the unauthorized use of Henrietta's cells. The contribution Henrietta made to the world should produce also some financial benefit to her family. Everyone has profited except Henrietta and her children. It would only be fair that they should receive as well.

    Posted by Gerri on February 1,2010 | 06:00 PM

    The interesting thing about this article is that the "contribution" that so many are talking about was NOT a contribution at all. Henrietta Lacks had no knowledge that her cells were being taken by her doctor at the time and therefor did not consent to having them play a vital role in history, nor did her family or closest relative, her husband, give his consent after her death for these cells to be used in ANY way. Granted they have done so much good, but at what cost to the family? The idea that "what they don't know won't hurt them" is ludicrous. Doctors can't play God with human cells without one's knowledge or consent. Who knows if the cells are truly immortal or not ( as stated by Colleen )...Time only will tell and saying that they are immortal or if they simply have outlived Henrietta doesn't make it so. We'll simply have to wait and see, although if she died in 1950 at the age of 30 and her cells have suvived so far, that makes them 110 year old cells and that sounds pretty immortal to me.

    Posted by Laura on February 1,2010 | 06:00 PM

    I heard of this story in school 1969 Weekely reader and again in my kids weekley reader This story hasenet changed

    Posted by mary on February 1,2010 | 06:00 PM

    Absolutely fascinating story....I am wondering if her cells could be used to clone her? Not being familiar with cloning, it is just a curiosity of mine.....but to think what an contribution this woman made without ever knowing it is just amazing to me......

    Posted by Shirley Baxter on February 1,2010 | 06:01 PM

    Fascinating article!

    Posted by Amber on February 1,2010 | 06:01 PM

    Scientists should use their 'own' cells when possible to do so to avoid problems.

    Posted by Dave L on February 1,2010 | 06:01 PM

    there is nothing sinister nor needful of monetary reimbursement needed here and i think much is being made of nothing

    Posted by susan on February 1,2010 | 06:01 PM

    Although this story is fascinating and shows how AFRICAN AMERICANS continue to make history and serve to be Beneficial to the human race (HELLO!), i have a HUGE problem with the author's choice of words to describe the family. why does it have to be "POOR Black tobacco farmer", exposing that her husband only had a 3rd grade education,or why did she have to put the disclaimer in the article about her brothers only being interested in the cell research because money was involved??? I dont get that! this is a huge breakthrough and great story for not only African Americans but for the human race period. the explotation of the family was uncalled for and made. maybe if Racism didnt exsist in the the 50's and blacks were NOT banned from institutes of learning, her husband would have recieved higher education and wouldve been able to understand the situation at hand and not be refered to as the husband, with a third grade education...Now lets talk about that! overall Im proud that this research has been revealed and YES THE FAMILY SHOULD BE COMPENSATED !!! Thank You and Good Day!

    Posted by Stacey Branham on February 1,2010 | 06:01 PM

    Great discovery and research. I hope that the family of Henrietta Lacks will be properly compensated in order to have better lives. It's their mother's best legacy not only to her family but to the medical world as well.

    Posted by Linda R. Balaguer on February 1,2010 | 06:02 PM

    Does everyone know where their biopsy tissues end up? Laws are now much different than in the 1950's. Mrs. Lack and her doctor's are longer with us, to confirm any conversations. Imagine being given that diagnosis. If a doctor told you that they couldn't save you, but that they would like to study the tumor in hopes of someday saving someone else, who would refuse? The doctor who obtained the samples couldn't have known of their characteristics at the time. This was not some racist, elitist plot. Too bad some people are focusing on money, rather than remembering her for the lifesaving legacy she left for mankind.

    Posted by Ann on February 1,2010 | 06:02 PM

    I noticed some people say the says are not immortal they just outlived her. This is not true as long as they are properly taken care of, they are actuall immortal. They are cancer cells so they usually circumvent programmed cell death. They also have an active telomerase enzyme, which prevents the telomeres from shortening. Which mean the DNA never shortens (Meaning runs out), so they cells can divide forever. These are actual immortal cells. also someone else mentioned that they were not sure the family should get resitution for this because people who donate their bodies do not. What you seemed to have missed while at the same time as saying it is that those people donated their bodies, gave them up. She quite literally had her cells stolen from her. Also sorry if this double posts.

    Posted by gregory on February 1,2010 | 06:02 PM

    I wanna buy this book! very interesting to read. I wish that it is available here in the Philippines.

    Posted by dexter on February 1,2010 | 06:02 PM

    i dident kno tht could happen to a person thts very inseresting.

    Posted by on February 1,2010 | 06:02 PM

    That was the coolest piece.

    Posted by ann on February 1,2010 | 06:02 PM

    What a story!!!! Great work!!! You should write a book on this matter.

    Posted by Mark Douglas on February 1,2010 | 06:02 PM

    Compensation makes sense to me. Its not a case of abuse, but in view of her contribution to humanity, it makes moral sense. What I'd like to know is if any scientist has determined why Henrietta Lacks's cells have lasted so long? Could her cells be holding the missing links to longevity? Her contributions to humanity may have only just begun.

    Posted by Joseph Keogh on February 1,2010 | 06:02 PM

    I say BLESS miss HeLa and her family....
    Just goes to show the poor get screwed again....
    All the money made off of this poor lady and
    her family does without....SHAME!!!

    Posted by David on February 1,2010 | 06:02 PM

    WOW, TALK ABOUT KEEPING YOU IN THE DARK, WHY NO ONE INFORMED THE FAMILY THAT AFTER, ALL THESE YEARS ABOUT THE USE OF THIER FAMILY GENES. I THINK THE FAmily should be paid for every year they were not told about research

    Posted by CAROLYN on February 1,2010 | 06:03 PM

    Come on, folks! It's wonderful that this woman has been given recognition - her name and place in history is now truly immortal. To say that the family is owed money is preposterous! The mistake the first doctor made was not to get permission, but this was long ago, before the ramifications of what this line of cells would mean. And we constantly learn from history, and from our mistakes. Informed consent is now necessary for this kind of use, and only now, would it be considered abuse. So let's keep this in perspective.

    That cells from her tumor were able to be used in so many research breakthroughs is the reward in itself - the monetary value of them came from the hundreds of thousands of hours put in by researchers and their grant-giving institutions, medical facilities, etc. as they became a commercial commodity.

    To be angry that the family wasn't 'compensated' for the use of the tissue, is typical of our generation where we feel someone is either a) to blame, or b) owing us something. Henrietta died young, that's the unfair tragedy. And yet, her death, unlike billions of others who live and die in anonymity, has been redeemed by subsequent events and achieved value more significant than any celebrity or rich person could hope for. And that is the real story here. Her payment, her family's payment, is that she is now recognized for her contribution to the advancement of medical science.

    Posted by mom with cells to donate on February 1,2010 | 06:03 PM

    Amazing story congrats on your achievement. Being a black man I'm so proud to here the HeLa cells taken from this black woman has helped so many people in ways her family probably will never realize. Though I can understand how they feel about being compensated, they are truly missing the point of how those cells have helped the medical community. Sounds like a greedy attorney at work to me. Anyway they should be honored, I'm sure Mrs. Lack is smiling from the heavens above knowing her cells have saved so many. Can't wait to read the book.

    Posted by E.J. on February 1,2010 | 06:03 PM

    That's crazy but yeah the family should get paid a lot of money for this becuase the scienist "took some of her cells without her knowing" that does seem like a lawsuit for the poor family!

    Posted by Kat on February 1,2010 | 06:03 PM

    Great story.I assume the cells didn't die, because the scientist kept them alive didn't they? Can't wait to buy the book

    Posted by jackie on February 1,2010 | 06:03 PM

    Please, let's don't make this about race. It just happened to be a black woman whose cells were used. They're lucky if they do get some compensation, and I think that would be nice since they need it. Plus, the writer will probably give them some profits, and it might be turned into a movie. The intrigue makes it that much more intesting.

    How many other people's cells are used. I wouldn't mind at all. I guess it would be nice to be told, but if it benefits science and humanity. I think the scientists thought it was no big deal to use the cells.

    Posted by Del on February 1,2010 | 06:04 PM

    I believe this is a very interesting story and with that being said I will read the book. I would like to say that this opens our eyes and make us more cautious about paperwork that we may be signing at any health care practice because we never know why different test that may be taken from our body as a result I think we should ask questions about everything.

    Posted by Kimberly on February 1,2010 | 06:04 PM

    When is the movie coming out?..title: Looking for Hela

    Posted by Cool on February 1,2010 | 06:04 PM

    I agree with the person above. WOW!!! Every break thru in each thing needs a starting point. God bless this woman. Sad that her family did not know and did not benefit from this research but we all did. Thanks to her and the Researchers who found the benefits that we all now enjoy.

    Posted by Eddie Davis on February 1,2010 | 06:05 PM

    Great Story. I hope the family can look at this as their mom was able to be part of history and maybe able to save other lives. But.....they should have been told about this sooner.

    Posted by Patti on February 1,2010 | 06:05 PM

    Why did these cells last so long? is it because they were from a cancerous organ which is possibly more likly to be a source of for lack of a better term stronger cells? not to descredit the young lady but cancer is what I think to be the real credit here

    Posted by troy on February 1,2010 | 06:05 PM

    Greedy family only wants money. What a joke this society is.

    Posted by Fredson on February 1,2010 | 06:05 PM

    This story reminds me of the Tuskegee Airman. It is a bitter sweet story.

    Posted by La Donna on February 1,2010 | 06:05 PM

    This story is completely misleading. Scientists do, in fact, understand why Henrietta Lacks cells were immortal. This story makes it sound, and judging by some of the comments a lot of people have read it this way, as if she was some kind of mutant with incredible cells that never died. In fact, the reason the cells were immortal is because they are cancer cells. HeLa cells were the first commercially produced tissue culture cell line, but now all cultured cells are derived from cancerous tissue. Cancer cells are immortal, they have no Hayflick limit, a value ascribed to all cells that determines how many times they can divide before they die. It makes them incredibly useful for research purposes, for the reasons stated in the article. However, researchers do also use primary cells, which are non-cancerous and not immortal, directly from a tissue source. It is not fully understood how the cancer cells are immortal, though it is thought to be something to do with telomeres which cap the ends of our chromosomes, these gradually get eroded over time in normal cells. I think this has the potential to be a really interesting story, describing the role Henrietta played in making biomedical research what it is today. I don't believe that what the doctor did was acceptable by today's standards and the way the family were treated subsequently was appaling. However, despite how it sounds in the story all the doctor actually did was to take a sample of her cancer (a biopsy - a common procedure) and study it, in doing so he made an incredibly useful discovery, enabling scientists of my generation to make use of these cell lines to make important discoveries. Nowadays, a doctor would fully explain to a patient and ask them to sign a form allowing their tissue to be used for scientific research, and they would have the option to decline. I wish journalists and authors would get all the facts straight before writing stuff like this.

    Posted by Jane on February 1,2010 | 06:06 PM

    Great Article, I never knew whom contributed in making great strides in modern medicine. Her family should be compensated for her efforts. I definately will be buying this book, I will have to talk to my sister in law regarding the use of her cells, I am sure she knows of it, she has a PHD in micro-biology and has done research on the nervous system and how it relates to paralysis. Fascinatiing subject.

    Posted by Debbie on February 1,2010 | 06:06 PM

    Thanks for a very interesting story - I learned a lot from it. We owe scientists so much for their work, not to mention the sacrifice of all the people who have suffered and died, and their loss helps the rest of us. Writers, please don't say your interest is "peaked" - it's "piqued".

    Posted by Dorothy on February 1,2010 | 06:06 PM

    Very Interesting, but our Medical Research has been based on the results from cancerous tumor cells? That doesn't make much sense to me, although this sounds like a great read.

    Posted by D.Benn on February 1,2010 | 06:06 PM

    I think it not to be amazing that you people say that she is not owed any money, but have not denied the fact that the company have made billions off of the black woman cells. This is racist and the aforementioned statements are racist as well. This woman family should have received a great percentage of the profits that the company made. This is the very reason why America will die.

    Posted by Anita on February 1,2010 | 06:06 PM

    This is a good story to tell, but it couldn't have been any more uninformed and unscientific. I once read about this while doing a project coming up with a research grant proposal. First of all, we have a pretty good idea of why the cells are immortal. If I can remember correctly the cancerous cells they collected had high activity of telomerase, an enzyme which rebuilds telomeres. Telomeres are the ends of the chromosomes which help to stabilize it and prevent chromosomal degradation(damage to the DNA). When cells replicate pieces of the telomere are lost which eventually leads to genomic instability after so many replications (this is what leads to aging). Her cells had telomerase which could therefore keep her cells from aging. This isn't some miracle enzyme though because it also leads to cancer(excessive cell growth).

    The other thing the author doesn't mention is that this is not some unheard of phenomenon. Bacteria and other single celled organisms are technically immortal because they can undergo multiple divisions and survive (this is because they have circular chromosomes which replicate more efficiently). Also, we all have cells that have similar qualities. They are called germ cells (sperm and egg cells) as well as stem cells and these are also immortal (not subject to loss of telomeres) or else we wouldn't be here.

    Posted by A. Bio-Undergrad on February 1,2010 | 06:06 PM

    I heard about Mrs. Lacks in Biology class too. I have used her cells in school. What people do not realize is that when a surgeon cuts out a cancer, the cells are often cultured. Certainly the cells are studied in several ways. They can be cremated or disposed of in other ways. I am almost certain that if Mrs. Lacks was asked whether she wanted the tumor to be given to her she would have declined. (Think about it...yuck!)
    Up until quite recently, no one bothered to ask whether tissue could be used. Now, it is routine paperwork that any tissue becomes property of the institution, to be used for research. Most people sign it without thinking about it. In either case, Mrs. Lacks, I am certain, has other things on her mind than was someone going to culture her cells. After all, she was dying of cancer.

    Posted by Carlos on February 1,2010 | 06:07 PM

    Fascinating story, but some of the comments leave me perplexed. A great start to Black History Month? A great accomplishment? The poor woman simply had cancerous cells removed. That she happened to be black does not make her a relevent part of the story. The cells are the issue, not her race, or whether the family was "compensated". They were diseased cells for crying out loud. They needed to be removed.She does not have to be deified for being sick, nor for providing a tissue sample.If you feel led to compensate her family, send them a check. More than likely you have benefitted from her cells as well.

    Posted by Wes on February 1,2010 | 06:07 PM

    The culture that the scientists used to preserve the HeLa cells must be its natural habitat.That culture must be compatible to some rare cells... i t has got to be developed .!

    Posted by Astrid Catolico on February 1,2010 | 06:07 PM

    What joy to see such a miracle revealed. My daughter is studying cells in school and this was such a treat for her to share with her class.

    Posted by JCB Mom on February 1,2010 | 06:07 PM

    Probably the most frustrating part of this article though is the idea that Henrietta is still alive as a person. By that logic our ancestors are still alive because they're sperm/egg cells gave life to us (granted it is not the exact same genetic material). But this gets into an interesting discussion. What do we consider to be alive, or a person, or an identity? This is what the pro-life movement doesn't seem to realize; that the issue is a lot more complicated than a zygote = soul = person because technically our germ cells are just as living as a zygote. Is our identity just our genetic material? That can't be true because we all know identical twins don't consider themselves to have the same identity. I say it is our mind and ability to reason. (Btw the question whether her mom feels pain was so ridiculous it makes me sad).

    Lastly, the racial aspect of this is pretty unnecessary. Sure it was probably not right to use her cells without her permission but I doubt her race played any factor in that and they had no legal concept of ownership of DNA back then. These days offering a tissue sample won't get you much money so I can't imagine the family would get much regardless of how useful the cells have been. Really they should be happy that their mothers cells have the potential to help so many people.

    Posted by A. Bio-Undergrad on February 1,2010 | 06:08 PM

    From the picture of the couple they do not look poor.

    Posted by Jerri on February 1,2010 | 06:08 PM

    she is probably also the largets person ever, if you took all the cell reproductions into account. It reminds me of the cartoon 'Akira' :D

    Posted by ada on February 1,2010 | 06:08 PM

    good article

    Posted by Ron on February 1,2010 | 06:08 PM

    Well the cells must not be that immortal, she is dead.

    Posted by Steven on February 1,2010 | 06:09 PM

    Why is it always about the money? I think that if she knew a small part of her cancer helped save one life she would be dancing in heaven. Dance Angel Dance

    Posted by david on February 1,2010 | 06:10 PM

    Amazing! After reading this I also want to buy the book!

    Posted by Rebecca David on February 1,2010 | 06:10 PM

    The story is very interesting & I believe that we are all connected...please stop worrying about who gets compensation. Because the doctor decided this on his own- is the reason for the amazing discoveries...if this had happened today perhaps Henrietta would have said "No" & there would have been no story! If the money still concerns you, anyone wonder how a poor woman was in a top hospital? Maybe the book will reveal more about many questions we still have...great story!

    Posted by Liza Carlson on February 1,2010 | 06:10 PM

    just like Americans always thinking about cashing in. How about all the money spent by medical research in developing those cures. Those cells didn't do that they were just a tissue sample in a dish. Don't act like H.L. developed it all. Fortunes may have been made but were spent as well.

    Posted by Luke on February 1,2010 | 06:11 PM

    I,m sure there are thousands of other stories out there that hasnt come to light as yet..Also sure that black people were used for a lot of testing as they do with animals nowadays...back then blacks were not even considered to be humans...remember tuskegee?But why would they want to let those cats out of the bag..because i,m sure the ones behind those experiments are the same ones that are highly respected in the scientific,pharmaceutical and medical books.

    Posted by lorna on February 1,2010 | 06:11 PM

    WOW THIS IS TRULY AN AMAZING STORY.

    Posted by maryam on February 1,2010 | 06:11 PM

    It,s very interesting I would like to read that book also.

    Posted by Madeline Canty on February 1,2010 | 06:11 PM

    It's so beautiful story make me to love my family more, I love science, so this stoy I love it, wow!! amazing that how tiny cell can do extraordinary thinks, we all need a web connection, we others depending on each one, in nonliving to living thinks and last for best people. Earth we need,sun, tree, animal......
    Makes worderful web food, living.....
    But a what way for science.

    Posted by lailablue on February 1,2010 | 06:11 PM

    i agree that tissue donation is just that - donation. but even in plasma donation, you are compensated for your 'time'. anyway, the book is available at lots of places, go to booksamillion.com and type in skloot, its $17.

    Posted by mary on February 1,2010 | 06:11 PM

    a great read. it is sad that her family wasn't given any money sooner.

    Posted by Cyclonus on February 1,2010 | 06:12 PM

    This is a fascinating story, though I wish the author had disclosed the outcome of the family's pursuit of compensation! This reminds me of a case I studied in law school, where the plaintiff won on the grounds of informed consent (they took cells without him knowing and made millions of dollars worth of products, etc.), so hopefully this had a similar happy ending.

    Posted by Caroline on February 1,2010 | 06:12 PM

    Thank you for the story. Certainly, it is fascinating. And of course, the family should have received royalties, as beneficiaries of the estate of the subject whose essential organs were being used -- even if initially in minute quantities. The scientists get paid, after all. They don't work for free! A woman contributed a vital component to their research -- her family should earn royalties, just as if they had contributed access to land for an oil company who earns revenue from the oil it extracts. Most disturbing of all, of course, is the issue of respecting someone's religious beliefs. If a person believes they have a soul, that soul dwells in every part of the person's body. If some part is maintained in a semi-living state, with biological functions taking place, it could be argued that the person has not been allowed to die completely. Some part of their soul may still be "in service" here. So there has to be 100% full disclosure and consent from the participant in the study. If full consent had not been obtained, because full disclosure was not deemed necessary, then the scientists who have ever used HeLa cells are indeed liable for damages to the estate of the incompletely deceased woman. They have to provide some formal process for dealing with Henrietta's actual Remains -- the lab cells -- and not just be dismissive about the whole thing. There are serious statutory concerns here, for example, with respect to embryonic tissue, the remains from abortions and so forth. Every human has Dignity and is entitled to a respectful conclusion of their earthly presence.

    Posted by Maria Ashot on February 1,2010 | 06:13 PM

    This story is amazing. I want to know more. I love the history and the human aspect of the story. I told this to my 9 year old son and he was equally amazed. Thank you for sharing this with us.

    Posted by Marcie McGowan on February 1,2010 | 06:13 PM

    Very interesting, to say the least! This is one of the most interesting and well-written articles I have read on my computer.

    Posted by Dr. Edward Dillowe on February 1,2010 | 06:13 PM

    All anyone cares about is whether they got paid.
    How about, some lady who was dying anyway actually ends up being the source of life for others.
    They ought to be proud their mama helped save lives, not look for a handout for something they had nothing whatsoever to do with.
    This kind of avarice has suborned the degaradation of the African American in this country into welfare recipients. Get them used to taking a hand-out, instead of earning it. Then they're easier to control, cause they know where their food is coming from.
    How about an organ donor? Should my children demand compensation from someone who my organs save, if they happen to make money? It's ludicrous and would open the door for more greed.
    Some things should be considered the right thing to do. Such as giving to medical science to further the live-saving efforts of the medical profession.

    Posted by philanthropist1 on February 1,2010 | 06:13 PM

    ECELLENT PIECE OF HISTORY AND YES IT SHOULD BE SHARED IN TODAYS SCHOOLS TO DEMOSTRATE THE CONTRIBUTIONS MADE BACK THEN BY ALL, AND THE IMPORTANCE OF THIS KIND OF WORK SCIENCE IS MOVING AHEAD IN FOR MANKINDS PROGRESSION INTO THE FUTURE, IT IS NEED..FOR CURES AND VACCINATIONS TO INSURE WE STAY A STEP AHEAD OF DISEASE AND ILLNESSES OF THE 21 ST CENTURY./ GOD BLESS THAT WHOLE FAMILY AND THE PRESENCE OF THEIR DEPARTED FAMILY MEMBER WHO HAD SUCH AN IMPACT ON MANKINDS BETTERMENT AND SURVIVAL IN TODAYS DAY AND AGE.

    Posted by CHARLES HAGER on February 1,2010 | 06:13 PM

    i'm only fourteen and i'm already interested in these kinds of stories! i saw this in yahoo and i was like, "is this really true?" This article is awesome! i wanna be a scientist someday.

    Posted by ronnie on February 1,2010 | 06:14 PM

    Complete and udder nonsence , maybe there is a cancer type cell that lived but as far as the person in the article, I highly doubt it and see this whole article as propaganda for some agenda that is unknown to me.

    Posted by Robert Gionet on February 1,2010 | 06:14 PM

    Amazing story! I am very interested in reading the book and seeing the resulting movie. How awesome. The family should be compensated in my opinion

    Posted by Pamyla on February 1,2010 | 06:14 PM

    The compound that the scientists used to culture the HeLa cells must be very compatible with such rare cells,making it as the cells' natural habitat..THAT culture must be developed to preserve cells that are compatible with it.

    Posted by Astrid Catolico on February 1,2010 | 06:15 PM

    Rebecca, I've been waiting for Ground Hog Day just to be able to get this book! Congrats!!!!!!! I even reminded people today that it was coming out tomorrow. Your hard work has come to fruition.

    Posted by Allison on February 1,2010 | 06:15 PM

    i really liked this story! i learned something new...loved it

    Posted by babyshirl on February 1,2010 | 06:15 PM

    wow very interesting i wonder what is up?i am only 12 so i wuoldnt understand half of it but i would try

    Posted by savana gallardo on February 1,2010 | 06:15 PM

    Very interesting story, I never thought that cell tissue from a poor black woman could have played such an important role in scientific history.From all the successful discoveries that have taken place from the use of her cells and her family being as poor as they are you would want to think that there is compensation for that family.Whatever the case may be this is a very good piece of african american history being shared with the world.

    Posted by Ronnie on February 1,2010 | 06:15 PM

    Fascinating.

    But, if I understand correctly, the original cells were from a tumor, so the basis of much of our knowledge about human cells came from cancerous cells? Can that be right? That's kind of a scary thought.

    Posted by Howler on February 1,2010 | 06:16 PM

    Our tissues are taken all the time and we do not know what happens to them after testing for strep or after a biopsy. They take a throat culture or remove tissue to see if it is cancerous as in this case and who knows if it sits there growing for years afterwards. I am sure that she probably said that it was ok for the doctor to see what was wrong with her and she had a pap smear which is cells or tissue being scrapped. All of us women have had it done for years and I could care less what they do with what they got from me!
    It is a cool story but I am not so sure that they STOLE cells without her permission?? She has contributed lots to our scientific advancement and I would think that she would be very proud of that fact!

    Posted by Carol on February 1,2010 | 06:16 PM

    The family does *not* need to be given any money. Forget that. It's not "injustice".

    Cellular material is not owned. It is not your property or your families after you die. It's just random strings of DNA floating around like a hundred trillion others.

    If the family wants to charge money for their cooperation in further studies, then fine. That is their right.

    Posted by Jim Brickman on February 1,2010 | 06:16 PM

    God bless science

    Posted by IsaaCerritosc on February 1,2010 | 06:17 PM

    THIS IS WHY IT IS IMPORTANT NOW DAYS TO BE AN ORGAN DONOR.
    WE CAN CONTINUE TO LIVE ON THROUGH OUR CELLS. I FOR ONE HAVE O-NEG BLOOD, MY CELLS ARE UNIVERSAL, HOW GREAT IT WILL BE WHEN IT'S MY TIME TO GO, THAT I AM AN ORGAN DONOR FOR THE GOOD OF MANKIND AND NOT FOR SELF-PROFIT. WHAT A SAD STATE OF MIND HUMANS WOULD BE IN IF WE REQUIRE TO BE PAID FOR BLOOD DONATIONS THAT SAVE LIVES. IN THE 50'S SCIENCE WAS JUST BEGINNING TO DISCOVER THINGS ABOUT THE HUMAN BODY AND HOW IT CAN HELP FUTURE GENERATIONS. WHO KNOWS HOW MANY MORE OF US COULD BE THE NEXT LIVING CELL DONOR.

    Posted by ginger on February 1,2010 | 06:18 PM

    This sparked my curiosity!

    Enjoy!!

    Posted by Kim Tuyen on February 1,2010 | 06:18 PM

    I think that perhaps, the HeLa cells could be ONE of the most groundbreaking "discoveries" in the modern Genetic Research. To actually have cells that are, if it is true(and time will tell), immortal is absolutely astounding.

    Posted by Mike Alfaro on February 1,2010 | 06:18 PM

    I'm not a scientifically minded individual. However, this article has sparked an interest to read the story of this woman and her family. I now find myself curious about these cells and the impact that they had on the medical community. I'm curious about Henrietta and her family. A poor farmer from Virginia...did she ever think for a moment that she would have a major impact on the WORLD?

    I AM going to read this book!

    Posted by GwenH on February 1,2010 | 06:18 PM

    Will Ms. Skloot see to it that the Lacks family gets their fair share of the proceeds from her book? They are AT LEAST entitled to THAT!!

    Posted by bigbearfromtx on February 1,2010 | 06:19 PM

    Great Story, But Again, It ends up being the "White Guys" fault! Why not just celebrate the triumph of science and medicine that was shared by all ?

    Posted by Louis on February 1,2010 | 06:19 PM

    Very fascinating article. I have one little comment:
    I have never seen a better illustration of why Strunk & White said "Form the possessive singular of nouns with 's. Follow this rule whatever the final consonant. Thus write,Charles's friend, Burns's poems,the witch's malice".
    So,the title should have read "Henrietta Lacks's ‘Immortal’ Cells\"
    and NOT Henrietta Lacks' ‘Immortal’ Cells . Needless to say, it looks like you've written a massive article about how someone lacked 'immortal cells' .......
    One reads the title and wonders why poor Ms Lacks lacked immortal cells.

    Posted by tom on February 1,2010 | 06:19 PM

    I knew about this. This is scary and factual. They have always studied black women. I promise you, it's hard to prove who cells are who outside the scientist community. That being said, it is and has been a racist issue. Why is HIV running out of control in the black culture only to passed down as a stigma of poor CULTURE behavior?

    The same way they study how to cure diseases, they can also cause resistance to them. The same way they knew that they were dealing with uneducated people who wouldn't have the understanding, you make them feel safe, then you take without knowledge of knowing. They did not care about the long term effect of the family, PERIOD! They were amazed that a black women(being the time period) something in her that they couldn't find in White women, otherwise what is the BIG SECERT!

    Posted by Ra on February 1,2010 | 06:20 PM

    Very Interesting story, BUT incomplete..The writer left out a bunch of stuff. I would Love to know the whole story, but would not pay for a book if this is all that is in it.. There is a Beginning a Somowhat Middle and Confunsing for what the ending is , or Might be...Great but left me with to many un-answered questions.. Dose anyone know if the Author gjoes on to tell the Whole Story??

    Posted by Debbie on February 1,2010 | 06:20 PM

    I knew somebody would be taking the racist slant on this story..surely somebody can find an angle to file some racist/politically-correct/hate lawsuit......it is the American way isn't it?

    Posted by gward on February 1,2010 | 06:21 PM

    It took a considerable amount of time for the world to hear about the Henrietta Lacks story. The rewards the world received from her contribution to science far outweighs the compensation the family will probably ever receive. Excellent story - long overdue.

    Posted by Joyce Pleasant-Crews on February 1,2010 | 06:21 PM

    This is a great story about how someone help the greater mankind and did not want anything in return. How do we know that she did not tell the scientist they could have them and use her cells anyway they see fit to help mankind out. Just like 90% of the families in the US they don't care anything about it until they mention they might be some money involved then they are like vultures to dead meat. Her and her husband may have agreed to let them test the cells and use them. It because in the 50's no one knew much about any kind of cancer it was all the stone age to us. If it help the people develop the polio vaccine like it said then something should be compensated for but as for using it as they see fit to help the better of mankind not just themselves. The polio vaccine has save millions on millions of lives since the 50's..........

    Posted by danny on February 1,2010 | 06:21 PM

    Gee, let's see now . . . The HeLa cells were taken from a tumor. MAYBE THEY'RE CANCER CELLS. That's why they don't die!

    Posted by Guildersleev on February 1,2010 | 06:22 PM

    Great story and I agree whole heartedly with Alina's comment.

    Posted by EVELYN B. PITRE on February 1,2010 | 06:22 PM

    If they could create a line of immortal cells, possibly in the future correct any problems with cells and genes through much more research, we'll we some day be able to live disease free, cold and virus free, and totally healthy for as long as we can afford it ??

    Posted by Michael on February 1,2010 | 06:23 PM

    this is awsome! but seriously i like how you said their is a human behind every expiriment.. gosh the brother of deborah sounds ....( ) yeah..

    Posted by Kathy on February 1,2010 | 06:23 PM

    I just wanted to say that I am 57 and have also had benefits from her cells, I had polio in 1955, and the vaccine helped me, so thanks to her cells, I was helped. I just want to say Thank you so much, Morrie

    Posted by Morrie I. Sparks Reeves on February 1,2010 | 06:23 PM

    This is a great story in the name of science and medical advancement. However, this woman cells were taken from her w/o her permission!! The Holy Blk Book calls that stealing.
    This is why they tried to cover it up for so long. Does the end justify the means? Not even if the powers that be decide to compensate this family. There should be an apology first to this family, than full restitution for what I consider total abuse and medical usury.

    Posted by Marshall Leonard on February 1,2010 | 06:23 PM

    This was an amazing story. I too, agree that the family definitely should be compensated. Would love to hear more about this.

    Posted by Loraine Legg on February 1,2010 | 06:24 PM

    Yes it's about race. People are used without their permission so they don't have to be compensated. People don't want to share that it was a Black woman that made all these contributions. It's a shame. This story albeit very informative casts such an awful light on Black People just by the way it's written.

    Posted by Bea on February 1,2010 | 06:24 PM

    thank you Henrietta and God bless your family.

    Posted by teri on February 1,2010 | 06:25 PM

    Excellent article. Makes me all the more grateful for knowing where my health care may stem from. I hope the family finds peace in all this debauchery. Money is a greedy business and heaven knows this is a huge huge lawsuit that im sure "the man" is going to try and avoid paying.

    Posted by Michele on February 1,2010 | 06:25 PM

    The article is interesting so I am quite sure the book will be also. I understand there are other cells out there, but no research has been done on the cell contributors. When we have lab tests performed, are our cells also used (whether mortal or immortal)?

    Posted by Lonnie Williams on February 1,2010 | 06:25 PM

    Will the family get any portion of the proceeds from the sale of this book?

    Posted by RM on February 1,2010 | 06:25 PM

    I studied cellular biology, nothing is surprised. Cancerous cells grow more easily from normal cells. That's why they can grow in tubes while normal cells don't. Nothing is big deal, people.

    Posted by BV on February 1,2010 | 06:25 PM

    Sounds like the family should be payed. Lot's of money was made from this womens cells.It's not fair.

    Posted by Michael Griffin on February 1,2010 | 06:26 PM

    Stacie, Considering it is the first day of Black History month, it will be a "racial" story no matter what you want. I thought it was appropriate for today. That's the way it is.

    Posted by Shaye on February 1,2010 | 06:26 PM

    Hela's immortal cell is one divine breakthrough in the field of science and on how our genetics could heal humanities' diseases. I just wish the Lacks Family could be properly given a recognition for the great legacy Hela has contributed that has helped and will help future generations to come.

    Posted by Herland Bernardo G Gutierrez on February 1,2010 | 06:26 PM

    while in university, we used HeLa cells to observe cellular structure and was told about this story, how the cells don't die. if i can recall correctly, the cells have passed thousands if not millions of cycles of mitosis, showing no signs of slowing down. that's the basic definition of a tumor, cells that divide, reproduce rapidly and form a mass. her cells are different bc whatever triggers apoptosis is either damaged or non existent in those cells, so they keep replicating constantly. and to everybody asking about whether the family got compensation... she couldnt tell ALL the story in a web article, just enough to make everybody want to buy and read the book :)
    i will be searching the local bookstore for this also! it seems like a fascinating story.

    Posted by Joe on February 1,2010 | 06:26 PM

    There have been people whose bodies remained incorrupt after death.

    These are holy people, saints, such as St Bernadette, whose body can be viewed, since it is kept in a glass case.

    St Bernadette's body has remained incorrupt. It does not decay. There are several others.

    I wonder if Henrietta lived a sin free life?
    I wonder if she was a woman of God?

    Posted by Fred on February 1,2010 | 06:27 PM

    I WONDER IF THE SPIRITUAL IMPLICATIONS OF THIS STORY CROSSED ANYONE´S MIND. WHAT THIS STORY REVEALS IS THAT THE MERE THOUGHT OF CELLS REMAINING ALIVE AFTER THE DEATH OF THE DONOR FOR SUCH A LONG TIME IS BEYOND SCIENCE AT THE MOMENT. SOME INTEREST MUST BE GIVEN TO THE POSSIBILITY OF A SPIRITUAL INTERVENTION WITH THE HELA CELLS.

    Posted by Victor Bennett on February 1,2010 | 06:27 PM

    I am in no way trying to be negitive, but study that picture. I would have never guessed that they did not have money. A very good looking, well groomed, well dressed couple. It is also a shame that no other or better picture survives of them.

    Posted by Lillian on February 1,2010 | 06:28 PM

    Thank you Henrietta Lacks

    Posted by lex on February 1,2010 | 06:28 PM

    This is an amazing story but disturbing in a way. I have been in medicine and know that the way things were in the fifties are in no way the way they are now which is both good and bad (confidentiality and the HIPPA laws). Anyway, what was more disturbing was the notation that these cells were cancer cells and that they could float on a dust particle and contaminate other cultures...Perhaps cancer IS contagious.... Just a thought. What if Dr. Simoncini is right and cancer is indeed a fungus which can do all of the same...especially be contagious....but like I said, this is all just a thought..

    Posted by marvenia on February 1,2010 | 06:28 PM

    I have to agree with the comment that only in America would profit or money come up as the major point people are taking from this story. Mrs. Lacks's legacy is unparalleled in the field of medical research, and her story should be taught in school to every child. As for the question of whether she was treated, in the 1950s there was NO cure for cervical cancer. They probably discovered that she had cervical cancer only because she was pregnant with Deborah, and had a prenatal exam. Henrietta Lacks could not have been helped, just as many women today with cervical cancer cannot be saved. But she saved so very many other people, and her family should rejoice the fact that their mother is a hero. She didn't know it at the time, but patients in those days never were told what was being done with their tissue specimens, whether they were black, white, or any other race. The final result of Mrs. Lacks' life is that her children still live, and that millions of others do to, just because of her. Why isn't that enough?
    Thank you, thank you to Henrietta Lacks and the doctors/researchers who made something wonderful out of her tragic story.

    Posted by H. Appel on February 1,2010 | 06:29 PM

    interesting - how is it that I'm a biology major and have never heard of this though...

    Posted by Lisa on February 1,2010 | 06:30 PM

    Henrietta was more than her cells. She has done more for humanity than she intended but more importantly we owe her eternal gratitude. It is so wonderful linking the cell to the person, the real being. Hearing of her, knowing of her is so sweet! Thank you for your research

    Posted by ram mohan on February 1,2010 | 06:30 PM

    Ms. Lack was not a "great" or "amazing" woman, but her body was endowed by God's nature with an amazing, evidently almost unique makeup. If her cells had this "immortal" quality there are possibly others. Have any others ever been discovered since hers? It would be fascinating to know.Even though nothing illegal at that time may have been done, the moral thing would have been to notify her family immediately upon this unique discovery and with a court appointed lawyer set up some sort of fair compensation for her survivors. It's not too late to retroactively get them a fair and just settlement from all who have profited monetarily from her cells unbeknownst to her family. At the very least, they should be able to "clawback some compensation, and certainly should be able to benefit going forward. This is truly an amazing story, based on our fount of accumulated human knowledge.

    Posted by William on February 1,2010 | 06:30 PM

    This is a very interesting article and I plan to share with amy 13 yr old daughter who is interested in science.

    Posted by Kattia on February 1,2010 | 06:30 PM

    I suppose there was no existing law on ethical use of biological tissue or cell samples at that time..Still, the family must be compensated one way or the other, and who knows, maybe one of them may have inherited his/her mother's unique biological genetic disposition..
    Personally, though, it is amazing how her life was able to help millions of people..talk about being an "accidental heroine"..God bless her..! Kudos to the writer for her guts and tenacity in pursuing the truth..

    Posted by ladyserendipity on February 1,2010 | 06:30 PM

    This is a wonderful article, about an unusual circumstance. It shows science as being teachable, and that's good. It shows a young black woman, mortally ill with cancer, who's tumor cells pushed forward the knowledge-base of human pathology. 1950 was a whole different world. The whole racial equality movement was not yet established. Scientists did not know about professional privacy rules, or about ethical disclosure issues. Certainly, they did not know about the bevy of lawyers ready to pounce on their experiments in the name of racial equality, which exists today and equates to litigious coercion.

    I can just imaging Jackson and Sharpton, marching in front of Johns Hopkins Hospital, with a bunch of sign-carrying do-gooders "making things right" for poor Henrietta Lacks, who never saw a dime of the money made on her cells.

    Is America aware of how many black scientists were involved in cell-reproduction back in 1950? So, any research on Henrietta Lacks' cells would have been billed as "WHITE American scientists taking advantage of a poor black woman's body parts, for profit, without compensation for the poor donor." Remember, no one got rich or famous on these cells. Things were simply back then. Most people just did what they were taught to do. Not closet racism, or unfettered misogyny. Just scientists doing what they did best.

    I'm so glad those cells were taken BEFORE the maelstrom of white hatred seized America. Now, at least the most of the culprit-scientists are dead, their predecessors can only build on their findings, hopefully without paying retribution to people who never even knew Henrietta Lacks.

    Posted by sisao tresed on February 1,2010 | 06:31 PM

    It truly is a good piece of writing, but what I didn't find out; did the family ever get any money out of this research with her invaluable cells? They should.

    Posted by CJ Stevens on February 1,2010 | 06:31 PM

    Even though the cells were taken without her knowledge (so they say). Everybody and there mother is worried about compensation. What about doing something for your fellow man woman or child without asking for something in return!

    Posted by Tell Me Why? on February 1,2010 | 06:31 PM

    This family will certainly have crowns in heaven.

    Posted by Helen Kircher on February 1,2010 | 06:32 PM

    Even though this is very interesting to me, shouldn't the family receive some sort of compensation for her DNA to be taken without her consent?

    Posted by Harold Morris on February 1,2010 | 06:32 PM

    This was a very captivating and mind-trapping piece of work. I never knew about HeLa cells before this day. I, like many others, will be purchasing your book. Nice work

    Posted by RaShai on February 1,2010 | 06:32 PM

    I only hope that when i am sixty or seventy that there will be a cure for mostly every form of cancer out there , so that people of all races can live and get more of life

    Posted by Black Friday warehouse on February 1,2010 | 06:32 PM

    never ending cell

    Posted by glenda on February 1,2010 | 06:33 PM

    If her cells are immortal, then her DNA must be very interesting....

    Posted by Michael on February 1,2010 | 06:33 PM

    Very interesting story! This woman has helped millions of people. I would love to do that! While I think it was unethical to not tell her, back then there wasn't the oversight in place to ensure this didn't happen. But think if it didn't happen how many people may not be here. She didn't need the tumor or cells. My daughter has cancer and we donated the tumor to science with the hope that it may cure someone or prevent the type of cancer eventually. I think this is a wonderful example of how something so small means so much to so many people. If she was my family member I would be so honored. The truly great things are done without money. I wouldn't want to receive payment for helping someone else!

    Posted by Angie on February 1,2010 | 06:34 PM

    The Lacks family will be compensated by Skloot from the books' royalty and the information she solicited from Deborah,being deborahs' intellectual property.

    Posted by Astrid Catolico on February 1,2010 | 06:34 PM

    Not sure if we should be thanking Helen as it appears to be another issue of a white man taking from a black person and turning her life into a multi-billion dollar industry. I really wonder if her family received a large portion of the revenue received from the research and from this book.

    Although the medical advances in this article and book are facinating, how they went about obtaining it was horrible.

    Posted by Sharon on February 1,2010 | 06:35 PM

    My only hope ,unless suggested already is that some portion of each book sale should be gifted to the family members in however small amount. If sales are over the top, so much for the better. One of President Obamas campain statements was that America has a deficit of empathy, let us begin to change that and what better place to start.

    Posted by John McCaffrey on February 1,2010 | 06:35 PM

    Very Interesting; read all the paperwork the Doctor ask you to sign these days ! They ask you to sign paperwork when you enter there office basically letting you know they will share your personal information and take samples etc. WITHOUT YOUR PERMISSION ! Our Country has given doctors a license to Kill and get by with it. They even protect them with you can only sue for a certain amount even though they have done irreplacable damage to your body !

    Posted by Sissy on February 1,2010 | 06:35 PM

    Mrs.Lacks family should receive money.

    Posted by Nell Spann on February 1,2010 | 06:35 PM

    Saw the book available on Amazon

    Posted by Beth on February 1,2010 | 06:35 PM

    WOW

    Posted by Sadie on February 1,2010 | 06:35 PM

    Like many of the comments, I would like to read the book. She was a beautiful women. She has help many ,because of her immortal cells,so she lives on helping to save lives. Her family should get something from the testing of her cells and a percentage of the book too.

    Posted by Anita Walker on February 1,2010 | 06:35 PM

    how many researches throughout the years were black??? were there any at all?? or were they not permitted to attend med. school? the researchers were all white males!!!

    Posted by pearl lufrano on February 1,2010 | 06:35 PM

    All, Save your money. Don't buy this book. All of the information is on Wikipedia. I'm guessing the Author isn't telling anything new. See : http://en.wikipedia.org/wiki/Hela_cells

    Posted by Tom on February 1,2010 | 06:35 PM

    Very interesting article. I had never heard of this woman before. Don't waste money on the book, the family probably won't receive anything from it. Instead watch the wonderful free BBC documentary at: http://topdocumentaryfilms.com/the-way-of-all-flesh/

    Posted by Kim on February 1,2010 | 06:36 PM

    Im sure when Henrietta had cervical cancer, doctors didnt know how to treat it, maybe tried to remove all the cancer they could, kept it to study. But what has bothered me for years is that if a doctor is powerful and so passionate about his study, im sure many people have been used for research in the past. And im even scared to endorse my license because if too much is known about you, how much is your life (body parts) worth to someone rich wanting to live longer. And tobacco was booming back then, why were they poor. I cant even see a tobacco farmer being poor now, half the people i know still smoke.

    Posted by Lo Lo on February 1,2010 | 06:36 PM

    Wow loved the story. I will definately look into purchasing the book it will be very interesting to know everything with detail...

    Posted by vanessa on February 1,2010 | 06:36 PM

    Fascinating story. Has the makings of a great film if promoted properly. Family would certainly be entitled to some percentage for ownership of the name and therefore the story. I will be looking for the book. Hope Ms Skloot has considered what her book sales can mean to the family.

    Posted by T.Labedzki on February 1,2010 | 06:36 PM

    Read the book, "Mutation" by Robin Cook. Even though it is fiction, you will be surprised how true this stuff is. DNA cell lines are in a number of labs throughout the country. Unfortunately you nor family is contacted, but it is often used. Think how often one gives blood or other tissues are taken for testing and sent to the lab. Where does the extra go? Is every single lab ethical? How do you know?

    Posted by B.P. on February 1,2010 | 06:36 PM

    It sound very interesting it touch my heart and my soul,but the worst scenario is for 25yrs.the scientist keep that secret to Henrietta Lacks family how greedy they are!They take the cell w/o permission.But.. how sure that the cell they experiment is 100%safe to human and no bad reaction in the future.

    Posted by Cecile Polancos on February 1,2010 | 06:36 PM

    Very Interesting.

    Posted by Masterkyle on February 1,2010 | 06:36 PM

    Wow! This is such an inspiring story to the imaginative and scientific mind! See how much people can discover? I love the story, though I do hope the family has received money from this, and if they haven't, should! Although I don't like the way they took tissue from Henrietta without her permission.
    Oh. And I can assure you all that she was NOT a vampire. :) Thanks, Henrietta, you have saved many lives, and I hope your family is proud.

    Posted by jayjay on February 1,2010 | 06:37 PM

    This was an interesting story, I am also 30 and was diagnosed with the same thing. Maybe my cell's could someday help others.

    Posted by Mel on February 1,2010 | 06:37 PM

    I would love to read this book. I lost a parent as a small child and can relate to all the wonders that deborah had as an adult. I am naturally interested in reading this book.

    Posted by mspeyron on February 1,2010 | 06:37 PM

    I'm always amazed by the willingness for people to dismiss the perversiveness of racism even when we're discussing the past. Did the author not say that the doctors took this woman's tissue without her permission and knowledge. There is a whole history around the use of Black women as scientific guinea pigs in the medical history in this country. The people responsible for this all benefitted from the thievery of this woman's body part. Now we're trying to write it off because of the good that was reaped from this? The people who initiated this had no care or concern for Henrietta Lack. They didn't care about her or her family. They were racists. Henrietta Lack is virtually unknown to the wider world. There are probably countless others like her in the medical history of the United States and probably all over Europe as well.

    Posted by Nana on February 1,2010 | 06:37 PM

    I was absolutely was intrigued by this story. I also see the point that this family should be compensated for quite a bit. There are cells from all kinds of families out there being researched on, but the difference is, that it stays anonymous now, as it should. It would be impossible to compensate everyone and their families. On the other hand Henrietta's family have been notified and even have been asked for their DNA. This opened up allot of emotions to this family, and I believe this is why they should be compensated.

    Posted by Stef on February 1,2010 | 06:37 PM

    Unbelievable story !

    Posted by karen1956 on February 1,2010 | 06:37 PM

    I have to say this story has many parts to it. First and formost Henrietta Lack Black Female(An Entreprenuer being a Farmer in that time) Farmer in the 1950's where racism was high and a lot of Black Farmers were cheated out of what they rightly should have received for their crops. How much treatment could or did she receive because of lack of finances and her skin color. Many, black people were turned away from hospital and if they did get to one they were not treated as human beings should. The Doctors, lack of care or concern about Henrietta knowing that he took part of her body(cell) to use for science study shows in human treatment, whether he thought she was going to die or not. Secondly, the Health condition of Henrietta Lack having Cancer at such a young age as a Black Female(as well as other in US) tell us even back in those time though it may not have been as high cervical cancer was effecting women in the Black Community much like today. How Far has science come in dealing with that issue for all women; detection, treatment, especiall given the Health Care Issue Bill.
    Third, For her family not to know about it for years is unexcusable regardless of public reaction to the sample came from a black women. It is Now 2010 get it together America Scientist etc. this was a Huge contribution and it can not be minimized or sugarcoated. People in this day in age get paid for research done to them even their contribution, why should Herietta Lacks Family be any differnt, It is not greed, it is called given HONOR WHERE HONOR IS DUE. She is not alive it should go to her family with interest.

    Posted by Lyssa on February 1,2010 | 06:37 PM

    Wonderful story, would keep on reading if there were more. Thanks to Helava person that has given the world such a gift, thanks Ms. Henrietta Lacks for helping me and my children avoid polio and other catastrophic illnes. For the scientist that took the cells, shame on you and thank you also, that tells you that doing the politically correct thing is not always the best thing to do. Wether the scientist did it for self gain or for benevolent or intuitive reasons, is left to his own concience.

    I'm a donor with the DMV and I would rest more in peace if someone else could benefit of any of my body parts or cells for scoentific experimentation. I can't use them any more, might as well help your niece, dad, cousin or my own descendants.

    Thanks again to all that make us human and to the investigative writer that keeps us in-touch with obscured parts of our past. Capitalize with the beauty and simplicity of things instead of looking at the ugly posibilities, we have the ugly part of life to reminds us daily of how inhumane some humans are.

    Posted by Maria Cheverez on February 1,2010 | 06:37 PM

    Not a good article at all, this person is totally unaware of their presuppositions and biases.

    Posted by Thomas on February 1,2010 | 06:38 PM

    Amazingly wonderful breakthrough to modern science helpful to mankind

    Posted by Bong on February 1,2010 | 06:38 PM

    This is a fascinating piece, it just shows that God made us all of one flesh, despite race. Race should never be an issue. It fascinates me to know that such a small amount of DNA could have contributed so much to medicine.

    Posted by Hayley on February 1,2010 | 06:38 PM

    Has anyone considered the idea of sainthood? immortal cells sounds like sainthood. After death a saints body will not rot,and that could explain an immortal cell!

    Posted by jeff on February 1,2010 | 06:38 PM

    I don't mean to sound insensitive to this person, her family, or this situation, but why would someone be compensated for something that SCIENCE discovered? She or her family did nothing to "find a cure" or what have you. If I had a gene in my body that cured all diseases, should I, or my entire genetic family be compensated? I think not!

    Posted by Kraven MacGregor on February 1,2010 | 06:38 PM

    We live in a time of momentous scientific leaps; a time when it's possible to sell our eggs and sperm online for thousands of dollars; test our spouses for genetic maladies and even frame someone for a genetic crime.

    We live in a time when one fifth of all our genes are owned by someone else, and an unsuspecting person and his family can be pursued cross-country because they happen to have certain valuable genes within their chromosomes...

    this is from Michael Crichtons novel "Next"

    HeLa story is not that surprising .

    Posted by william hart on February 1,2010 | 06:38 PM

    This family does NOT need to be compensated in any way. Her cells were used just as anyone else's who has ever signed a consent form to have surgery, just as was stated by another poster. There additionally, were no such laws back then regarding the matter. And further, I find the scariest part of the story is that the cells were used at all given that they were infectious and cancerous at any rate(as stated by an earlier poster. Strangely, there cancer was a very rare disease also back then. Wonder how it spread to become one of the most prevalent in our times? Use your heads people. Don't get caught up in the drama.

    Posted by Andrea rutledge on February 1,2010 | 06:39 PM

    This was a very good article. Looking forward to the book. Thanks.

    Posted by Daniel Feaster on February 1,2010 | 06:39 PM

    WOW MAYBE THIS CUOLD BE A CURE FOR CANCER OR SOMETHING LIKE THAT MAYBE? =) that would be cool! =) but thats sooo cool that her cells are still living! i wish i had cells like that! and how rotten those people are the faimley deserves money for their mothers cells!

    Posted by hannah on February 1,2010 | 06:39 PM

    Great story, but I am saddened to hear all those out there saying that the scientists "owe" her family something. These were cells removed from a cancer patient, that normally would be biopsied then discarded. Who would scream for money cause they "discarded" het cells without permission. Has this use of her cells harmed anyone..no. Has it helped save lives..yes. Let the Memory of this young women be enough to carry us on, not the greed of money.

    Posted by deb on February 1,2010 | 06:40 PM

    Wow, very interesting..I want to go buy the book asap. Thank you for sharing this with everyone, and thank you to the family to letting you get this story to share.

    Posted by Sue Knutson on February 1,2010 | 06:40 PM

    Another example of how a great contribution from African Amercans was stolen and they did not get the credit for during their time in history.

    Posted by John on February 1,2010 | 06:40 PM

    Please let's not make this a race issue. The story about this lady who has her cells "donated" without her knowing it is awesome. Because of her, scientists know more about the diseases and how to cure it. I like to think that there is no malice in the heart of the scientists who took samples of her tumor, not the healthy cells from her body to further the knowledge and understanding about cells and diseases. I do not judge her descendants for trying to get at least some monetary compensation from the folks who used her cells. I think they are entitled to something but I am not sure how much and who will pay them. That issue is muddled in my opinion but hey, its their relative whose cells they are using. Give it to them. I think nothing is big enough compensation for their dead relative's cells being used in medical research. Let's be glad the cells have no nerve endings and cognition or memory to actually know what is being done to them in the name of science and knowledge. Hooray for Henrietta! God bless her soul.

    Posted by Wren on February 1,2010 | 06:40 PM

    A fascinating story, but I'm curious as to why the family thinks they should be compensated.

    The scientists were working to save or prolong her life. Given the circumstances I expect the Doctors did not get compensated.

    The tissue would have otherwise been destroyed.

    Doubtlessly, a benefit has been accorded to the medical world at large.

    I expect that at the time doctors were testing tissue from any source they could. Frankly, I wouldn't be surprised if the physician taking the sample hadn't simply asked his patient for consent, that is not the sort of thing that gets recorded and years after the patient and original researcher have passed away any facts relating to consent from those vastly more informal times is purely speculation.

    In any event, giving the doctors a bias or improper motive for sample collection while they were working in a research hospital famous to this day for its charity work is merely absurd.

    It is unfortunate that the the family in question is still destitute some 60 years after the fact, but certainly that fact can't be attributed to any research or researcher.

    The author has written an original work of literature and is entitled to any profit that comes from it.

    In any event, I do look forward to reading the book.

    Posted by Kramer on February 1,2010 | 06:40 PM

    It would be nice to know how the cells were kept alive. Refering to FRANKINSTINE ( It's ALIVE)

    Posted by gary whittington on February 1,2010 | 06:41 PM

    Compensate the family? Why don't you see if you can get the address of the family and write them a check. Everybody is quick to donate somebody else's money but just a few will share from their own pocket.

    The doc is dead so "sue the dust and let the rain settle it."

    The idiot who wrote about the Tuskegee experiments was lying. While there was experiments on black folk with syphilis, those with syphilis were treated with the best known drugs at the time. That is just another urban myth. Some people just believe whatever fits their template; some will believe anything.

    Posted by BIG CHEVY 3600 on February 1,2010 | 06:41 PM

    Why would she have died if her cells were immortal?

    Posted by Anna on February 1,2010 | 06:41 PM

    Story was amazing. So fascinating!

    Posted by phil on February 1,2010 | 06:41 PM

    by immortal im guessing it means that they don't die with age, because there heas to be a WAY to kill the cells, nothing is completly immortal

    Posted by alex on February 1,2010 | 06:41 PM

    wow.very interesting article. I would like to buy the book.

    Posted by grace on February 1,2010 | 06:41 PM

    They (the Lacks') don't appear to be "poor farmers" by the looks of their clothing, they seemly are dressed in upper-middle class garments....not like the "poor pauper" tobacco farmers discribed, but rather educated society people from the Harlem Renaissance Era. Huumh...I think Mrs. Lack should rightfully take her place in the HISTORY books at the very least since they won't be reaping any other rewards. Her contribution has greatly advanced our medical discoveries

    Posted by P Titus on February 1,2010 | 06:41 PM

    I heard that the King Tutankhamen mummy had cells that were still alive when they examined his corpse.

    Posted by anthony on February 1,2010 | 06:42 PM

    Great story. They sure were very good looking people. They didn't look like any farmers I've known.

    Posted by Debbie on February 1,2010 | 06:42 PM

    Yes, a very interesting story.

    Posted by Tavie on February 1,2010 | 06:42 PM

    A remarkable story. Thanks for sticking to your plan on getting this told. So happy to read something other than the same old news. I hope Henrietta is somewhere smiling that we are talking about her and that she has helped advance science!

    Posted by David on February 1,2010 | 06:42 PM

    I remember reading this story in an Ebony magazine during the 70's. I suggest everyone read Medical Apartheid. The book should clarify race and medical experimentation.

    Posted by Regina on February 1,2010 | 06:42 PM

    Interesting story--cervical CANCER cells proliferate--that is, keep growing against the odds. Samples taken during that period may have been used without all the red tape that currently exists because it was test/waste tissue. Millions of dollars of Federal Money were spent BY all of us for the good of ALL of us--of every race. The pharmaceutical companies (for whom I do NOT work) have developed products using their own private funds to make a profit--as all businesses must, to STAY in business. I appreciate that HeLa's cells were used for a good purpose as have been cells and cases of many other people throughout history. I do NOT sense some "plot" or "conspiracy" to cheat HeLa. In fact, since the 1960's, trillions of dollars have been spent to lift up black people. We are ALL Americans and playing the race card has become a stale, cheap ploy to discard the idea that we are all equal in the sight of God and of each other. There are very few racist villians today although it seems many seem to want to profit by acting as if NO progress has been made. My family is multiracial and we know that ALL people are valuable. Quit the race baiting and paranoia, people! Thank you HeLa, Doctors, Taxpayers, and Pharmaceutical companies that gained valuable knowledge from these cancer cells which might have been simply thrown away.

    Posted by martij on February 1,2010 | 06:42 PM

    I WAS JUST AMAZED THAT SOME MANY PEOPLE READ AND POSTED TO THE ARTICLE. I PRINTED TO READ LATER, BUT BECAME CURIOUS AS TO THE NUMBER OF PEOPLE RESPOND. THIS WAS JUST AMAZING AND A GOOD READ.

    Posted by Brenda on February 1,2010 | 06:42 PM

    This is a great story, truly amazing can't wait to buy the book.

    Posted by Yajaira on February 1,2010 | 06:43 PM

    This article was great and I am interested in reading the rest of the story in the book, too. To Masnoh W., the "immortality" of Mrs. Lack's cells have nothing to do with her race (or being a vampire like idiots have commented) but everything to do with being cancerous. Her cells were taken from a cervical cancer biopsy and regrown in a labratory. As long as the scientists keep reculturing the cells so they have adequate nutrients to survive and multiply they will be immortal. If they ever stopped re-culturing the cells, they would eventually die out.
    Also, People are crazy trying to make everything about money. If I donate blood and its used in a transfusion to save a life, should I track that person down and ask for a check?

    Still, Mrs. Lack should've been given a choice.... and it is great that she will finally be given her place in history thanks to this woman that researched her story.

    Posted by maburget on February 1,2010 | 06:43 PM

    Clones don't look like the host. If you watch the sci-fi movies, you will believe that. Identical twins, who have the same dna do not always look alike. The traits may be the same, which would cause them to look similar. A clone may look as different as 2 complete strangers, though.

    I don't think the family should get one penny for the research. It hurt nobody to take the cells, and saved thousands, if not millions.

    Posted by Peter on February 1,2010 | 06:44 PM

    Its just crazy to think the scientists and the author of the book are just going to make mad cash and the whole time the family gets nothing. Just another example of how the rich get richer and the poor stay poor.

    Posted by justin on February 1,2010 | 06:44 PM

    I too find this article extremely interesting. However,back in the 1950 there was no such thing as compensating anyone. The laws have changed over the years, even though her cells still live, they were taking back in 1950. Most medical and science findings have happened through accidents or mistakes. Thank God the doctor did take the sample..look what it has done for the bio world. Even if he had told Henrietta, she probably would have never understood it...I would have never understood it back in the 50's. I can't believe how many people want money or try to demand something that really does not belong to them..now really think what it was like back in the 50's. I also have a question...how do we know that since Henrietta's cancer cell is still living that it has not spread the cancer to other people? Are we going to sue Henrietta's family?

    Posted by Lynn Bogle on February 1,2010 | 06:44 PM

    What a fascinating story. I too, like others are curious if the remaining family got any money from this. Guess I will have to buy the book and find out. Hopefully it's in there.

    Posted by Tracey on February 1,2010 | 06:44 PM

    I wood like to know how much mony is the family going to get from the book

    Posted by Rolo on February 1,2010 | 06:45 PM

    I'm really impressed with this story. Thank you for bringing it to "life".

    Posted by William on February 1,2010 | 06:45 PM

    The family should be compensated by the research and proceeds from the book. It's their Mom's legacy and her children and grandchildren should be rewarded!! Everyone else has made money, now it's the family's turn.

    Posted by Pat on February 1,2010 | 06:45 PM

    As a physician, I was fascinated by this article in many ways. It was tastefully written, with an emphasis on respect for the humanity behind all life-saving scientific research. I would love to read the book!

    Posted by on February 1,2010 | 06:46 PM

    This is so interesting. Black history is everywhere. Even places we would never imagine. Great story!

    Posted by carrie on February 1,2010 | 06:46 PM

    This is very interesting piece. I am not much on biology, but this helps others to realize and see that science is extremly important to our lives and even though we might not understand it, there are people out there who are actually trying to do positive things. BUT I do feel that because of all the positive things that have benefited from her cells, her family should have got something. Great article!!! Makes me want to buy the book!!!

    Posted by Kristy on February 1,2010 | 06:46 PM

    I truly believe she was an Angel in human form.

    Posted by Alice on February 1,2010 | 06:46 PM

    did family get any money? where can i gete this book?

    Posted by Juliya on February 1,2010 | 06:46 PM

    Now I'm no scientist, but if the reason her cells are "immortal" or do not age is because they are cancer cells removed from a tumor and we have been basing a lot of medical and scientific research on them, aren't we just giving ourselves cancer in some ways? I mean besides the research done against the cells looking for a cure, but basing medicine and slowly changing our genetics possibly resulting in evolution. Now this is pretty far out, but it seems like if were not careful we might just become a real human cancer, with the ability to go on forever as long as we have a source to sustain us. Hey wait a minute, we as species already kind of do that anyway....the cells were discovered in 1952, you say? That's almost 60 years...this is the part were someone says "Humans were not meant to play God", take that whichever way you wish...oh well my small minded intelligence is mere imagination when it comes to this theory. Save it for the funny books as they say... but I would laugh in my grave if it really ever came true. Think about it: the possibility of going from fish-creature to man typing on a computer, a nice incomprehensible theory which might have some substantial truth to it. How about a giant cancerous blob devouring worlds or something?. Oh by the way, if you don't believe in evolution: PLEASE COMPLETELY DISREGARD THE ABOVE STATEMENT OR AT LEAST FIND ANOTHER WAY TO JUSTIFY OR CONFUTE IT.

    Posted by prenups on February 1,2010 | 06:47 PM

    History, interesting.

    Posted by TamunaHela cells on February 1,2010 | 06:47 PM

    I think that this is a very interesting story. Creepy yet extreamly fun to read. this wonderful womans family is owed ALOT OF MONEY. Its just plain wrong that these people didnt tell her or her family im just totally appuled by that fact. Did ther family ever get the money? Are there any other cells like hers? Does her family have those kimd of cells? Did haveing cancer have anything thing to do with her cells? WERE CAN I GET THIS BOOK!?! And as for the cells floating on air, is that a bad thing? Can it give other poeple cancer? That seems a little scary. I cant wait to read this book!

    Posted by JONAS BROTHER LOVER on February 1,2010 | 06:47 PM

    i lost my parents to suicide and wish ther were some living part of at least my mother i could even if it was a culture. keep the reserch going and maybe someday who knows.

    Posted by devoid mccauley on February 1,2010 | 06:47 PM

    The Lacks' family need to be compensated millions of dollars

    Posted by Dee on February 1,2010 | 06:47 PM

    why does it seem to suggest that they were injecting stuff into the woman and doing experiments on her in one part and in the beginning it simply says she was a woman with cervical cancer?

    And why do some of you think that it was something malicious that white scientists did to a black woman? I would think that they would have had opportunity to take cells from white women with cervical cancer as well, and if they were so racist, as some of you infer, why would they keep alive cells from a black woman instead of a white person?

    The cells would have been tossed in the trash, just like an aborted baby is one million times a day, so get some perspective. Use your brain. Think on things good! Why be so racist and opportunist in your thinking?

    Posted by justicewins on February 1,2010 | 06:47 PM

    I can not wait to get a copy of the book to read. Very interesting..

    Posted by Amos Ajo on February 1,2010 | 06:47 PM

    Great just something else to hear about how the black man is getting ripped off.

    Posted by John on February 1,2010 | 06:47 PM

    Thank you for a super,super read. There is no way of thanking this Lady for her world wide contribution to millions upon millions of children that may have died and not reached adulthood,to read this wonderful story.

    God has his ways of justice,this is the perfect time for this book to come out as we have become more tolerant and understanding in this big world.I will buy the book to find out the results as there will never be an end to this wonderful story.

    Posted by M.C.McElligott on February 1,2010 | 06:48 PM

    VERY SCAREY WHAT THE MEDICAL COMMUNITY CAN AND WILL DO WITHOUT TELLING THE PATIENT. ALL FOR SCIENCE AT ANY COST.

    Posted by ROSE on February 1,2010 | 06:48 PM

    Absolutely fascinating. I look forward to the book!

    Posted by S Beckstrand on February 1,2010 | 06:48 PM

    In recognition to HeLa's contribution for the success of this story, part of the profits obtained from the book sales and all of the medical products should be offered to Henrietta Lacks family survivors.

    Posted by Ronald on February 1,2010 | 06:48 PM

    THIS IS REALLY AWESOME AND NEEDS TO BE SHARED WITH ALL. I WOULD LOVE TO READ THE BOOK.

    Posted by LEOLA AMY on February 1,2010 | 06:48 PM

    I have always thought I am a very unusual person and very superior in a lot of ways and I THINK MY CELLS SHOULD BE SAVED AND SOMEDAY MAKE ANOTHER COPY OF ME. not kidding

    Posted by THEMOJOMAN on February 1,2010 | 06:48 PM

    I always thought immortal cells = Cancer. That's what cancer is- when the cells don't die and instead continue to reproduce resulting in a tumor.

    Posted by christina on February 1,2010 | 06:48 PM

    This story is very informative. HeLa could as well be made a saint of cell biology for giving scientist part of her body as a sacrifice for the future of modern cell science in medicine and medical research. Some day scientists and those involved in cell culture will find a place for this innocent lady whose consent was not requested before the research was conducted on her. She should really be immortalized.

    Posted by onokpise on February 1,2010 | 06:48 PM

    immortality huh boy oh boy i guess mankind will not have his limitations after all very interesting story they say older is better LOL

    Posted by ramon on February 1,2010 | 06:49 PM

    I've been in biological research for many years and have used HeLa cells, and know of their origin. Now that I teach college biology and microbiology Henrietta Lacks is always part of the discussion when we're talking about tissue culture and transformed (immortal) cell lines.

    Well done.

    Posted by Paula on February 1,2010 | 06:49 PM

    This is a very interesting story even though it is not the same issue it reminds me of the story Miss Evers Boys. Experimenting on people or cells should be done with ones consent. The scientist need to be honest and give the family their proper share of monetary assets. They deserve it. My mother has never seen her mother so I really understand how her daughter feels.

    Posted by Lori Williams on February 1,2010 | 06:49 PM

    It's great the advancment they have made in science because of these cells. It gave scientist the tools it needed to find answers to vacines and many other unanswered questions.Due to the cell they took without her permission one good thing sometimes out weight others. I due hope that the family will get componsated for everything they have discovered because of the cells and not make a racial issue of it,the important thing is every discovery maid because of the cells. But the real tragdey was the mother passing away and not having her children know any thing about their mother.

    Posted by lulu on February 1,2010 | 06:49 PM

    Thanks foe so great an article, this is an ongoing thing in which the people of color Black, Brown, yellow and red has been expolted. The relatives should indeed be compensated for what was done without their knowledge, I for one wonder just how much has been payed to the holding institution for the cells used in the research, and how many times has as a result of new treatments and new medicins has been reaped as a rsult of the study of those cells. I for one think there is a great need to start from grassroots in rhe many millions that has been gained, while the family of the deceased lady continued to live in proverty. I don't think any of the things is a result of a racist idesl. But I do think it is a result of greed within the many corperations involved in the resarch.

    Posted by titus arnold on February 1,2010 | 06:49 PM

    The author may believe that race had nothing to do with this (although she never says that directly only infers it), it is telling that blacks were the only once that the scientists took cell tissue unbeknown to the persons. Cell tissue research has been and continues to be important to scientific progress,but in this case, it would seem that an apology and just monetary compensation is in order.

    Posted by glenn on February 1,2010 | 06:50 PM

    There is also another story about her, called "Modern Times: The Way of All Flesh" done in 1998.

    Posted by JP on February 1,2010 | 06:50 PM

    I wonder if her cervicle cancer had anything to do with being a tobacco farmer. It is posible there could have been evidence linking canceer to tobacco whit that HELLA CELL.

    Posted by Gasry Whittington on February 1,2010 | 06:50 PM

    Great investigative work. The family and bloodlines of Henrietta Lacks deserve some kind of appreciation from the use of their mothers cell. It saved thousands of other human lives and opened the door to discoveries we depend very much on in the current age of technology.

    Posted by nick on February 1,2010 | 06:50 PM

    The fact of the matter is, the doctor treating Mrs. Lacks did not consider her permission necessary. She was poor, she was Black, she was sick, and he was unconcerned with such formalities. She would never know, and he would be thanked for his contribution. The fact that her cells spawned a MULTI-BILLION dollar industry is significant, and because her cells were SOLD (and continue to be), not given away, is the very essence of CAPITALISM and her children's children's children ought to be compensated in her place for the benefits those corporations and universities reaped from knowingly tapping into stolen property. I learned of Mrs. Henrietta Lacks when I was a biology student in the 70's so there has been enough time for those having the means to do so to see to it that the right thing is done. Just because her cells have given the world scientific knowledge and done some good is no reason her family should not be paid when people unrelated to her have done so billions of times over. It makes no sense to cut her family, still in poverty, out of the deal.

    Posted by Pilar on February 1,2010 | 06:51 PM

    For further reading.

    Posted by Generoso Malabonga on February 1,2010 | 06:51 PM

    I would like to thank Henrietta for her gift to the world. How many of us would not be alive today if it wasn't for this woman. I will definately be purchasing this book. In response to ALINA, they did not take the cells after she died. They took the cells when she went into have a tumor removed. The cells were part of the tumor. This has NOTHING to do with using dead people for experiments. You need to do your homework on the subject and read the article again. You obviously didn't understand it the first time. Stop wit the scare tactics when you don't even know what you're talking about.

    Posted by Bobbi Porter on February 1,2010 | 06:51 PM

    I will be buying this book and a big Thanks to Rebecca Skloot's for being obessed enough to run with it and allow us all to read it.

    Posted by jess on February 1,2010 | 06:51 PM

    good story

    Posted by benstringz on February 1,2010 | 06:51 PM

    It's amazing that everything in life comes back to money compenasation......bad actions don't always equal money compensation...that's why this world is the way it is!

    Earn your money, stop sueing everyone and looking for a quick buck.We are talking about the 1950's. There were hardly protectoin laws for patients and no guidelines for doctors to follow. That's why we have hepa laws now.

    Taking her tissue without telling her is not integrous to say the least. Will money make that all better?

    what an amazing woman. Her ledgend is what she left and will always be passed on as a pioneer of modern medicine.

    If I were her family, that in itself would be enough. How proud I would be of her.

    Geez!

    Posted by lila jane on February 1,2010 | 06:51 PM

    This story is amazing! Myself and my mother will be buying the book. Helen Lacks is a modern day Lucy. My sincerest prayer is that the family is HEAVILY compensated. This story is reminiscent of the HBO movie, Something the Lord Made. The white doctor's family made millions off of this black man's ingenuity. A common story in American history. We will know when the color divide is no longer when families can finally get what is due to them. Great book!
    * I doubt Mrs. Lacks signed for or agreed to having her cells harvested. Therefore she didn't donate to science. Being a poor black woman, I'm sure the cells were taken and she was discarded.

    Posted by Tiff Sharpe on February 1,2010 | 06:52 PM

    god is working now and then!

    Posted by jerri nash on February 1,2010 | 06:52 PM

    ...all the more reason why we need more stem cell research as well. THINK of the potential of helping human lives...

    -Loretta
    http://www.TaiChiGala.com

    Posted by Loretta Wollering on February 1,2010 | 06:52 PM

    Back in the 30s they did not need consent to take cells. Cells back then are looked at like MS is looked at today. Something that is not understood. No the family should not be compensated because those are not the original cells. It clearly says they grew more cells. Those are the scientists now. Maybe they could get compensated for the original cells but back then it was not a law to ask to take cells. The story is great but it saddens me that the brothers only want to take a stand when they finally understand that cells cost money. Probably should have left that out makes them look greedy

    Posted by PG on February 1,2010 | 06:53 PM

    wonderful science! since we are all related by being human it comes as no surprise that one among us would be able to unite us all as one in the ability of her wonderful cells . and please remember these cells came from a cancerous mass! a cell mass which is a murderer of mankind and has been used in turn as a savior of our kind.the wonder of it all!!!

    Posted by sharon murphy on February 1,2010 | 06:53 PM

    I agree with Alina.You cant just take someones cells without permission its an invasion of their rights.

    Posted by anita on February 1,2010 | 06:54 PM

    What an excellent and awe-inspiring story! I applaud you and your tenacity for tracking this all down and involving the family as well. Family history--especially family medical history--is vital to our survival and is often not talked about amongst the older generations. My mother is adopted and we recently found out that her biological father and four of her biological mother's siblings died from colon cancer as well. This kind of information is vital to know and share with their physician during routine health screening.

    Posted by Lori Breit on February 1,2010 | 06:54 PM

    family should be compensated

    Posted by alice martinez on February 1,2010 | 06:54 PM

    Very interesting article! I guess I wil have to buy the book to see how it ends! It certainly poses the question of what could happen if they continue replicating/sharing the cells and if they might ever be used cloning. I also feel that the permission of the doner and/or doner family should be obtained. However, I do not necesarily agree payment should factor into it (similar to organ donation now) If however a sample is not destroyed after it's initial intended use, then perhaps some payment to the family should me made (sort of like royalties??) This of course is my initial reaction...further data and thought might change that. A sticky wicket indeed....

    Posted by KP on February 1,2010 | 06:54 PM

    I think it is sad that they take someone else cell and make billion of dollars. Never part it with her family. You know it is same thing they do with organs, When you donate your organs to save some else life, I like that idea but someone else has to pay thousands of dollars for the organs they got free. If someone don't have money or insurance, can't have the organs. This is all over the world. It's the same as giving your ideas to someone else and you turn around someone else making money off your ideas, you get nothing. It is unfair You know what, you should make a movie out of this story, you will be surprise that people wants to watch this movie

    Posted by Benjamin on February 1,2010 | 06:55 PM

    to the article: hmmmm....cool. Always wondered where the name HeLa came from.

    to the commenters: CAPS LOCK DOES NOT MAKE YOU LOOK SMARTER. Nobody really cares about the "immortal" tidbit. It's just a hook for you to read the article (and look, it worked).

    Okay. I'm done.

    Posted by mags on February 1,2010 | 06:56 PM

    Hi,

    There seems to be some confusion about HeLa cells that as a cancer researcher who has worked with HeLa cells I might be able to clear up.

    1) HeLa cells (like most other cell lines) are considered "immortal" b/c they contain mutations in their cellular machinery that allows them to grow outside of a human body and they reproduce at an extremely high rate many times.

    2) Researchers are able to purchase HeLa cells from companies like ATCC and make frozen stocks of HeLa cells that can be used at a later time. This means that as long as a scientist continues to make frozen stocks of HeLa cells they can continue to use them after their intial purchase of the cell lines.

    3) Over the years, scientists have made different variants of HeLa cells. For example, one HeLa cell line has been modified so that it contains green fluorescent protein (GFP).

    4) HeLa cells are some of the fastest growing cell lines available with an approximate doubling time of 16-20 hours. They are also some of the easiest cells to grow. These two factors make HeLa cells one of the most popular cell lines used in scientific research.

    Hope that answers some questions. If you are interested in more info such as price (currently $256/vial), growing conditions, etc. check out this website:
    http://www.atcc.org/ATCCAdvancedCatalogSearch/ProductDetails/tabid/452/Default.aspx?ATCCNum=CCL-2&Template=cellBiology

    Posted by Dan on February 1,2010 | 06:56 PM

    May the Gods bless HeLa, it is a shame she died so young but apparently she did not die in vain, she seems to be the ultimate "organ Donor" so to speak. She may have saved millions of lives. He family should be given restitution. It is just a shame they did not have all the knowlege back when they took her tissue. I can only hope to half live up to what Mrs. Lacks done for mankind. Again, bless you HeLa and your family. I would love to read this book. K. Rane.

    Posted by SpiritRane on February 1,2010 | 06:56 PM

    This is a very interesting article but I don't have quite the same reaction as many others do.

    It is amazing to think there might be a little bit of Henrietta in all of us! This story isn't about being black or white or asian. That initial sample could have come from anyone. Sad as it is, Henrietta was just another person seeking medical help with part of her treatment regimine being the taking of a tissue sample - just like countless others before her and ever since.

    After the lab workers determined she had cancer the leftover sample could have been dumped into the hazardous waste container and burned, but because of timing some research scientist probably needed a human sample - why waste it?

    It is obsurd to think the surviving family should receive any financial benefits because of this history. The article does not claim her cells are immortal, just that some of the cells were cultured and used to grow more generations. If they weren't helped out by the scientists they would soon die out.

    I would like to believe this woman would be enthralled knowing a small part of her has played such a great role in helping and saving countless others.

    Her family should be proud knowing that a bit of her is with each of us.

    Posted by Allen on February 1,2010 | 06:57 PM

    Not sure what the talk of monetary compensation for this person's family has to do with the story. Based on what is written above, a piece of her tumor was taken and some of it was used to start this cell line, the first successful human cell line grown in culture. What happened thereafter was a consequence of brilliant scientific work in using the cells for scientific advancement. If I were part of her family, I would be overjoyed that one of my ancestors' tumor served humanity so well. The talk of money here only comes to cheapen the story. This was part of a tumor, right? Was she opposed to donating that? I don't see the issue.

    Posted by Pete on February 1,2010 | 06:57 PM

    The main focus should not be just the powers of HeLa cells but the wrong and the invasion of the rights of her family. You took her cells without her knowledge and then made billions of dollars off this woman and never gave her family a penny.

    Posted by Priscilla on February 1,2010 | 06:57 PM

    To the lady named Nancy Salisbury... I am related to you through Daniel Boone. I believe we are 7th cousins... I have heard about this story down the line... I certainly wish I could help. But as time goes by.., more items seem to get lost and people pass on... I would so much like to talk with you. I do hope you find some kind of answer... Please contact me if you can... Rick lodestein1@yahoo.com

    Posted by Rick Lodestein on February 1,2010 | 06:57 PM

    Who paid her medical bill? Was she a ward of the state? Did she get proper care and did her family (husband) give consent for the cells to be taken so as to find a cure.

    Posted by on February 1,2010 | 06:57 PM

    I don't think that the family is entitled to any compensation. People go to academic medical centers to get treatment, but they also should understand that ongoing medical research takes place at hospitals such as Johns Hopkins. The monetary value of the HeLa cells is primarily the result of the hard work put into their study by the various scientists involved. It was mere chance that they came from one person and not another. Scientists at Johns Hopkins were absolutely doing the ethical thing by carrying out research on cancer and we have all benefited greatly from their long hours of labor.

    Secondly, the immortal cells are from the patient's CANCER. It's not some creepy situation involving clones of the actual person. They are mutated cancer cells.

    Posted by Bob on February 1,2010 | 06:58 PM

    EXCELLENT STORY I JUST WANNA NO WHY THE DOCTOR TOOK THE SAMPLE WITHOUT LETTING HER NO AND DID THE FAMILY FINALLY GET COMPENSATED

    Posted by KOOL KENDALL on February 1,2010 | 06:58 PM

    the diseased cells are multiplying and feeding off other diseased cells and multiply faster than current cells feed off older cells thus creating a perfect isolated ecosystem

    Posted by ch on February 1,2010 | 06:58 PM

    Henrieta Lacks creat a way for medicine yesterday and today why is her family in poverty may be because she was a black woman because i dont think it will happen to any other race, They would have been rich for generations to come thats not fair, If they didnt know then but now they do that family should be reward at list 50% of what they made off of henrieta lack cell.

    Posted by Life Johnson on February 1,2010 | 06:59 PM

    It is tremendously saddening to hear of the misfortune of the Lacks family, however, I find it unnecessary to compensate them for a scientists’ research. True, the cells did belong to their mother, but the only reason scientists had those samples in the first place is due to the fact Ms Lacks had cancer and required treatment. Giving anything to her family is wrong, and I would hardly call removing a piece of a tumor stealing, especially in the 50’s. It would be like Picasso asking a friend to take one of his paint brushes, the friend using it to create a masterpiece, and after Picasso’s death his child demanding a cut of the profit from the painting’s sale. I hardly think any single person made millions off these cells after all of the costs of research and running the labs in which the testing was conducted. I do believe the story needed to be told. The family should get compensation from the author for the interviews as well as any other shows or articles they choose to take part in hereafter. Doesn’t it seem wrong though, to pay this family for research they didn’t do, and wouldn’t have known about without the author prying for information? The author states “It took almost a year even to convince Henrietta’s daughter, Deborah, to talk to me.” and “Deborah’s brothers, though, didn’t think much about the cells until they found out there was money involved.” I’m not using the word greedy, but how convenient for interest to be taken as soon as the dollar sign is brought to light.

    Posted by Sean on February 1,2010 | 06:59 PM

    I can't believe that some of the comments have turned this into a racial issue. I also am infuriated by the greediness of alot of people. $$$$$$ Is this all you see. wow. How were the people that took that sample able to know all that it would accomplish. They didn't. so how do you compensate for the unknown. Yes she should have been told that her sample would be used for science, but I do not believe that she or her family should be compensated for the sample. I was asked during childbirth for the cord, they told me that it would be used possibly for open heart surgery, or some other good. I was elated to think that something that I did not need could possibly save a life, I would never ask for money for that. I loved to be able to tell my daughter, that she probably saved a life or two, or more. I think the anonynomy is best, unless of course the sample is used for the family itself. Don't we have to PAY a handsome sum to freeze our eggs etc. for use at another time. I can't believe there is not a line a mile long of donors of unneeded samples for the greater good of all mankind. Just shocks me. Thank-you was good enough for me.

    Posted by Dianna on February 1,2010 | 06:59 PM

    so basically : let me get this straight, a poor black womens cells were used for experimental purposes for over forty years and that is the most recent picture of her cells? really amaising! I thought they were circular, but her cells look like a person! this changes how I will look at things from now on. like dead skin cells, there are little versions of me scattered about all over! that is why detectives can find criminals using their cells! I totally understand now!

    Posted by decepta on February 1,2010 | 06:59 PM

    very Interesting. I was looking at the cells I wondered since her cells which were cancerous which they combined with other cells to come up with a polo vacine that everybody gets now. Does that mean that we all have cancer thriving in our blood waiting for one day to form into a cancerous disease? hmmmm I wonder?

    Posted by angie on February 1,2010 | 07:00 PM

    I hope the family does get some kind of compensation.
    However, there is a foundation to which anyone can donate money for scholarships for members of the family-
    http://rebeccaskloot.com/book-special-features/henrietta-lacks-foundation/
    Or you can donate directly to the family, there is a link to that website on the above page.
    Also, i believe the book comes out on Feb. 2.

    Posted by Alex on February 1,2010 | 07:00 PM

    show this family the money

    Posted by SHEILA on February 1,2010 | 07:00 PM

    How is this racism? I can't stand when articles feel the need to "jump to conclusion" for the reader. This is not about torturing a black woman (ridiculous) or racism. The properties of these cells which are scientifically important are due to their "immortality", not the skin color of the person they came from.

    People need to get over their selves and stop using racism as a reason or excuse ALL THE TIME... not everything is racism, and thinking it is, IS RACISM!

    Posted by Mike D on February 1,2010 | 07:01 PM

    In a way, she's a hero. Her cells have been used to study and research diseases and find cures. That's a legacy i think her children should be proud of. For her contribution to future generations, however inadvertent, she will always be remembered.

    Posted by Nina on February 1,2010 | 07:01 PM

    It is disappointing how whites use to treat under educated blacks back in the day. But to also hear that her family never received anything from the government for the work that she did and that they are still impoverished is very sad. Her family should be compensated for all that her cells help this world to acheive in medicine. I am so grateful that Hernietta Lacks was born to give others life and she was a black women like me. Thank you again Hernietta for blessing the world with your cells.

    Posted by Terri Bailey on February 1,2010 | 07:01 PM

    This story is incredible! It speaks volumes to me about the Justice of God. Here we see God's awesome ability to gift a lady (Henrietta) with an immortal gene. She got no benefit from it, BUT God saw 2009-2010, before she was born. Now her lineage is to be blessed with compensation, when they had nothing, and were poor people. Somebody prayed this miracle in, people! God is a covenant keeping God, and maybe Henrietta prayed, knowing she would die for God to bless her off-springs? Who Knows? Thank you Jesus !

    Posted by Jan on February 1,2010 | 07:01 PM

    I'd be afraid they'd (scientists) would come after her kids or the whole family for more cells. After all, we (people of african descent) were hunted for slavery purposes which made alot of people rich -- except us. And much of that "old money" is still at the helm today.

    Posted by Robin on February 1,2010 | 07:01 PM

    No the lesson here is that every human being blood & tissue used for Science should be signed off on by that individual and copy righted. Any moneys made off those samples,which I'm sure there has been,should be shared with the family.

    Posted by Ronald on February 1,2010 | 07:01 PM

    From what I found out from the internet in the case of Supreme Court of California case of Moore v. Regents of the University of California. The court ruled that a person's discarded tissue and cells are not their property and can be commercialized.

    So precedent pretty much makes a hard case for the family to get any money. Not that it is right, but I wanted to let people know about this.

    Posted by Candice on February 1,2010 | 07:02 PM

    The doctors that took this woman's DNA, made profit off of it, concealed it from her family, denied her family profit from it and further exploited her death by contacting the family after their deed was done for even more information and again not giving them money only points toward the pattern of behavior alreaady established by white people as self serving evil doers.

    Posted by infuriated on February 1,2010 | 07:02 PM

    The HeLa cells could have come from anyone's cancerous cells. She is only important because she is the one they happened to be taken from, which would have been done to study them anyway, under any circumstance when one is under a doctor's care. Her family is owed nothing - it is the people that did the work and research that rightfully owed the money from the research!!!!! Good grief people.

    Posted by Nicole on February 1,2010 | 07:02 PM

    This is a very facinating story. That bit that I'm not happy about is, why wasnt the family compensated. had it not been for this cells, many lives would have been lost. It's not late, the family should be compensated and thanks to the writer of this story for your publication.

    Posted by Immaculate .J on February 1,2010 | 07:03 PM

    What a wonderful article!!! I actually had a chance to meet with the Lacks family in 1995 (during the HeLa conference hosted by Morehouse School of Medicine in Atlanta, GA). And yes it is true that the family was clueless as to how vast Mrs. Lacks cells has contributed to scientific research and as quite as it's kept.... they/we will probably never know.

    KUDOS Sarah.

    Posted by Hannah Marie on February 1,2010 | 07:03 PM

    Wonderful artical. Cannot wait to by the book tomorrow.

    Posted by Tara on February 1,2010 | 07:03 PM

    Great article, what a small world. I'm not sure how I feel about compensation for anything. We are all human and it would be nice to think that people give just to better the human race rather than what's in it for me. I don't think the family is owed anything really but I'm sure a lawyer say's it differently, as he gets the lion share. Thank goodness for the risk takers!

    Posted by Scott on February 1,2010 | 07:03 PM

    My son & I really enjoyed reading this together. We had alot of questions, like many others, Did she give permission without really knowing it? We'll never know. Makes you think. We will never really know what the Dr. said, as time goes on, stories change. Her family's life could have been shaped a totally different way, if money that is made from this "research" was given to them. On a different note, I think that Henrietta should be honored for her contribution, and the wrong that was done should be brought out in the open. Forgiveness frees the soul. Good Job on the story, never give up writing, your good at it!

    Posted by ChristinaV. on February 1,2010 | 07:03 PM

    If she was my mom, I'd be proud of her contributions to the health of so many children today. Those original cells are long deceased but their spin-offs keep on giving hope to people everywhere in one form or another. God Bless her and her family. Let them be at peace with her beauty in the eyes of God. She was a chosen one.

    Posted by Daisy on February 1,2010 | 07:03 PM

    To those interested in reading the book, visit your local Public Library many will have this title. That's where I'm getting my copy to read!

    Posted by David on February 1,2010 | 07:04 PM

    We're all just "cells" in this Petri dish called Earth!

    Posted by Kelly on February 1,2010 | 07:04 PM

    Years and years ago - in the early 1980s, when Discover Magazine still put the year in their name, it published a complete article about Henryetta Lacks' cells and how they had migrated to ALL research cell sites worldwide. The article told how her cells discovered in cells provided by a remote research company in the USSR and about the lab tech who realized he was looking at cells that could not have come from Russia. ALL cell banks had to be purged and cancer research had to be started over from scratch. Researchers believed that all cancer were fast-growing, impervious to treatment, and always deadly....as it had been to Henryetta Lacks. The article gave me the impression that she was fondly thought of by the researchers and I know I came away wishing she'd had the same uncanny ability to survive as her cancer cells. Maybe someone can find a copy. For over 30 years I've sympathetically remembered Henryetta Lacks - a lady I never met.

    Posted by Carol on February 1,2010 | 07:04 PM

    This was and is a wonderful story. I had a daughter that had Cystic Fibrosis. She was 22 when she died, and from age 5 (when she was diagnoised) she spend days, weeks and months at a time in a teaching hospital. After this I wonder if there was any DNA tissue taken from her for research. I would love to know that in some aspect she was still alive. If they did infact extract I hope that it has helped in the advancement of treatment. I have a son that is in his 40s that also has Cystic Fibrosis. It would be wonderful if DNA from his sister is infact keeping his CF from being his death sentence. When diagnoised death was expected by age 5/6.

    I plan to get this book. I know that this woman's family needs the money from the massive amount that was made, however the research it's self takes a massive amount of money to keep going.

    Posted by joanna goodwin on February 1,2010 | 07:04 PM

    Very interesting story! Need to know more about this. Where can I buy this book.

    Posted by Carl Mendoza on February 1,2010 | 07:04 PM

    These medical claims using Hela cells are bogus. The polio vaccine was developed using egg cells, not human Hela cells. There has not been one single, solitary disease successfully treated or cured by Hela cells. In fact, Hela cells are known to be carcinogenic! That is, when anyone gets an injection of Hela cells, a cancerous tumor begins to form at the site of the injection! The future of medicine lays in your own "adult stem cells" that have successfully treated more than seventy different diseases! The Hela cells are a dead end that causes cancer!

    Posted by Physician on February 1,2010 | 07:04 PM

    How very ironic that a multi-billion dollar business was borne from a woman decades ago whose children can't afford health care insurance today.

    Posted by Robyn on February 1,2010 | 07:04 PM

    Obviously the scientist didn't know that these would be "wonder cells". It was just another tissue sample to be cultured, like thousands and thousands before.

    I wasn't around then, but I would guess that the way things worked in the 1950's were a lot different. There was certainly no DNA testing to identify a particular cell to a particular person, so there would have been no need for all the privacy that we now have.

    Posted by Jason on February 1,2010 | 07:04 PM

    Don't be ridiculous. Science dosen't owe anybody anything. Some roguish doctor took a tumor sample from a poor dying black woman sixty years ago to use for the greater good of humanity. Why does someone have to PAY her family now? I hate that mindset. You people can never be satisfied with the greater good, there always has to be money due someone.

    Posted by dspire on February 1,2010 | 07:04 PM

    The most significant part of this article was the fact her sons didn't care about their mother's cells until they found out there was money involved.

    Posted by allen on February 1,2010 | 07:05 PM

    So she is still alive?

    Posted by Kelly Son on February 1,2010 | 07:05 PM

    I dont think they will get any money.Y?Because there are thousands of people whos cells are used ,bought and sold.If they start giving money to one family,they will have to start giving to all families.They would loss money and in the end loss money for research.

    Posted by Amanda on February 1,2010 | 07:05 PM

    This has the makings for an outstanding documentary! I hope PBS would consider sponsoring the documentary and Henrietta Lack's is properly credited.

    Posted by Dave Armstrong on February 1,2010 | 07:05 PM

    I so do not like claiming the overused race card but, in this case I think at the very least there may very well be an element of that. Wheither its not mentioning the black man who invented the stop light, or the same who invented the filament inside the electric light bulb or, the first to create blood plasma, black peoples contribution(s)to our country, and this world, are often ripped off and sometime simply ignored. Part of hidding this womans identity and name seems to be more of the business of that very same racism. Fortunatly, many whites, and other ethnics have fought hard against racism and are to be credited for that.

    Posted by Brian on February 1,2010 | 07:05 PM

    Very, Very interesting. And the way it is portrayed makes me be so interested in the story.

    Posted by ArCo809 on February 1,2010 | 07:05 PM

    This was a very interesting piece. I can't believe all those years and the family didn't know anything. Excerpts like this probally would get more people to read and do their own research rather than take the word of someone else. Great peiece.

    Posted by Akilah on February 1,2010 | 07:05 PM

    Sounds like a beautiful story about a beautiful woman who has helped the human race. Too bad so many comments here are about monetary gain and not focused on the good that has come out of it all.

    Posted by Littlebit on February 1,2010 | 07:06 PM

    i am so glad this is getting this much attention. You are amazing for starting this at 16, I started my family at 16 instead of thinking of other people. Way to go!

    Posted by Sheila Buehler on February 1,2010 | 07:06 PM

    I Love this article. It's extremely interesting. I've never heard anything like it.

    Posted by Stephanie Hollins on February 1,2010 | 07:06 PM

    That is sooo cool! want to hear more!!

    Posted by Mia on February 1,2010 | 07:07 PM

    There is a whole movie on this you can find on YouTube. There are people on here who doubt her cells are immortal- it is a little hard to believe but if you do your research into the depth and scale of this womens' cell history around the globe and get the significance of what has transpired you will see that the scientist are not keeping them alive, they cannot control the growth, they just continually divide and grow.

    Posted by Jon P on February 1,2010 | 07:07 PM

    I hope that the family of Ms. Lacks can get some compensation from the researchers who so cavalierly sold the cell line. IMO, a person's DNA should not be bought and sold,unless the researchers who wish to get rich obtain permission and grant a percentage of the royalties to the person and their heirs.

    Posted by Tom on February 1,2010 | 07:07 PM

    Once more science proves that BLACKS are superior to other races.

    Posted by Andy Anderson on February 1,2010 | 07:08 PM

    great work you should be commended,but there a so many gold dggers in our country we have to remember that money cannot buy some things,why? because its priceless,we should all be thankful to the person who took the cell and usde it for good because without his part the cell would be dead as for the woman bless her soul and her family ,and they should be proud to know they have her genes and stop looking for money.

    Posted by jerry on February 1,2010 | 07:08 PM

    I think this is a very interesting story..but when you have any procedure done..and a tumor or a body part is taken..normally its properly disposed of or would be thrown away. in this case they used the tumor for testing. and to protect the woman's Identity, they named it something else.
    that doesnt mean the family should get ANY money from it. their mother didnt live on, she didnt die due to testing. she died from the cancer. plain and simple!!! I think that in this world everyone is out to get a dollar and thinks if you sue your entitled to something. the family knew nothing of it. the writer is just wanting to tell a story of how hela came about..that means telling about the woman behind it. that family isnt and shouldnt be entitled to one dime! the writer on the other hand should get paid for doing the research and writing a book....the dr who decided to do testing to learn about tumors and what they do is intitled...thats it in a nutshell!!!!

    Posted by tammy tillotson on February 1,2010 | 07:08 PM

    Great article indeed, the cure to most human diseases lies within ourselves, more research is needed. Definitely a book i'll buy when i see it.

    Posted by Art V. on February 1,2010 | 07:08 PM

    Similar to the Tuskegge Experiment.

    Posted by Nic on February 1,2010 | 07:09 PM

    I don't think immortal is the right word. Correct me if I am wrong but new cells are grown from the old in the culture "process" aren't they? Stem cell lines are preserved in the same way I think. And "HELLO" this was 1951 we should handle things better today so what is all the fuss about? The research possible because of this is what is important isn't it? Honestly some of the comments above are a waste. Whatever is done with my body after I die, no one will be owed any money. If I choose to donate my body to science or not my children certainly won't have any claims.

    Posted by Ron on February 1,2010 | 07:09 PM

    Whoa, thats kinda cool! Okay, really cooL!!!!

    Posted by Marisa on February 1,2010 | 07:09 PM

    I also found this to be of great intrest, and will buy the book. If the family is not compensated for one reason or another (the medical world could find a way to stop it)for the cell process. Would any of the profits from the selling of the book be shared w/the family?

    Ed Knoth February 1, 2010

    Posted by Edward Knoth on February 1,2010 | 07:09 PM

    My Oh My....
    This happen back in the 50s, and I bet what's good gonna come out of this article is Lawsuit. In other word, we are going to hear a lot about M O N E Y. That's right. This is a land of opportunity and every Tom, Dick, and Harry that's related to the poor woman is gonna ask for M O N E Y.
    Is there a Statute of Limitation on this case?
    Back in the 50s, one hardly hear much about lawsuits etc... Today, people are so greedy when it comes to M O N E Y. We may not hear it from the author but I'll bet you there is a case load of lawsuits being filed at this very moment. Tsk...tsk... What a pity? America, a Land of Opportunity.

    Posted by Jacques C. on February 1,2010 | 07:09 PM

    Being a nurse I found this very interesting. I am sure there were people that would have love to give the family some money but it would have opened a door that could not be closed .

    Posted by Lorie Fortenberry on February 1,2010 | 07:09 PM

    *Tuskegee

    Posted by Nic on February 1,2010 | 07:09 PM

    i think the world of science is like another dimension wherein a lot of secrets are hidden to our normal world. maybe HeLa was really alive inside the labolatory living with the room 45 species.

    facing the reality, the family do have right to know anf given a commision by the cells being sold. that would be more motherly love. let's just think that their mother have acct on a bank and forgot to give her last will to her children.

    Posted by GUINEZ on February 1,2010 | 07:09 PM

    The cells are cancerous- they were from a malignant tumor. Cancer cells have the ability to multiply forever, that is partly what makes them wreak havoc in the body. Are the scientists sure that tests on these cells would yield pertinent information to normal cells?

    Posted by A on February 1,2010 | 07:10 PM

    Yes, this is interesting, but the 50's were a totally different era. The legallity or morale implications weren't even a factor then. It was just research then, just that. Later I'm sure they discovered something was different with these cells that made it easy to regrow and culture them to establish a base line for research. Then they found the cells could be grown for other labs. This way all research being done would start with the same product and would be equal across the sciences. This of course became a business, it was not meant to maligne anyone. But this being the US everyone feels they are owed the world for everything. Even in this story clip it was said the family didn't care or mind until they heard her cells were being sold for research, now they feel they are owed large sums of money. Maybe according to our laws but are they really? NO!!! I'm a disabled unemployed man for 8years now, if these were my cells I would feel the same way. How do you know your cells aren't being used for research? You don't!!! Anytime you have any surgery your cells are sent to a lab. You have no controll after that unless you take them to the lab yourself and then destroy them afterwards. JUST BE PROUD HER CELLS DID SUCH GOOD FOR THE WORLD!!!!!

    Posted by David Kellams on February 1,2010 | 07:10 PM

    If this is the case there should be a cure to everything ?

    Posted by kathy on February 1,2010 | 07:10 PM

    does the book author intend to give a piece of the advance or profits from the book sales to Helen's relatives?

    Posted by me on February 1,2010 | 07:10 PM

    It will be good to read the entire story. I had read so much about HeLa cells but never knew quite what they were or from whom they originated. -- Now, when you have a cervical smear (as Pap tests are called these days), you are asked to sign a consent form that says any part of the tissue they take from you can be used for research purposes without compensation. (At least, at large institutions.)They should not have taken Henrietta Lack's tissue without her and her family's knowledge.

    Posted by Mary Chichester on February 1,2010 | 07:10 PM

    A+

    Posted by Rafael on February 1,2010 | 07:10 PM

    lol omg my name is Henrietta which is the first interesting part, nd i also thought that this was an interesting article.

    Posted by on February 1,2010 | 07:11 PM

    Maybe while we are at it, the lung and oral cancer survivors can seek compensation from the the family of Mrs. Lacks? I'm sure there are one or two with family living on the streets! Times are different and if you were to red the surgery consent you sign, I'd bet this issue would have been addressed. I do know that the lack of basic biological knowledge in this forum is pretty disappointing!

    Posted by ralph on February 1,2010 | 07:12 PM

    the cells were cancerous theres nothing unusual about them not stopping producing new cells for decades.

    Posted by Andrew on February 1,2010 | 07:12 PM

    Nancy Salisbury, try ancestry.com to see if you can find anyone who has him listed on a family tree. They might have notices on where he was buried, or the hospital might have records on which mortuary picked him up.

    Sadly, there are many stories of funeral homes not handling remains correctly, but hopefully yours is just a paperwork glitch.

    Posted by Rina on February 1,2010 | 07:12 PM

    I am saving this article for future reference. I continually find interesting parallels from the "medical" field from years past to the nuclear experimentation all done for the interest of science. My Father was the first human being to fly into the cloud of a hydrogen bomb cloud and without proper health safeguards. Please read "Plutonium Files" by Eileen Welsome for another good look into our miltary and civilians put in harms way by radiation.

    Posted by Doug on February 1,2010 | 07:13 PM

    @Colleen.

    When they say the cells are immortal they are not saying that one cell will live for ever. Instead immortal cells (immortal cell lines) are cells that will continue to grow and replicate indefinitely as long as they have adequate nutrients. Generation after generation (of the cells) will be the same.

    Posted by Josh on February 1,2010 | 07:13 PM

    I think human tissue samples for research should come under the same guidelines as donation of organs for those who give permission to donate their organs to those who need them.

    Posted by Keith on February 1,2010 | 07:13 PM

    I thought it was wonderful just to know the story. I had heard of it, when I attended Mt.Sanai School of Medicine, but this is great! And cloning doesn't bother me a bit. With all due respect to God and believers, what do you call putting Adam to sleep, and making another human being out of a rib? Sounds like cloning to me, but the difference is that it was done by the main Architect! Henrietta Lacks family should be proud of her. A High School should be named after her. Especially since so many inventions and great things were done by African peoples. Keep up the good work. And thanks, Henrietta Lacks.

    Posted by Victor M. Flores on February 1,2010 | 07:14 PM

    What makes this scientist a racist? Just because he's a white man. This was just a scientist and I'm sure a black scientist working on a white women would have done the same thing for research. I agree with Alina, maybe the families should give permission to use a family member's cell tissue. I would be very upset to see someone that looked like my Dad that died in 1988 on the street.

    Posted by James on February 1,2010 | 07:14 PM

    i liked the fact that people do care about the real feelings.

    Posted by chand on February 1,2010 | 07:14 PM

    People wake up ..Does immortality come from God or man..This fooling with the creation is insane.Have faith in God for your immortality, man can NOT provide it....Please think this through...Is there anyone out there who feels the same way? Or are we going crazy????

    Posted by Peter S Lazorchak on February 1,2010 | 07:14 PM

    I bet Mrs. Lack would be fascinated that a part of her went into space and is making such an awesome impact on life. Whether the scientist was racist or not, we don't know but God saw Mrs. Lack as great and he made her an "immortal" part of global history, humanity and great debates to come. It's humbling. Kudos Rebecca Skloot. The family should definitely be compensated since Mrs. Lack didn't voluntarily donate to science.

    Posted by Joy Bounds on February 1,2010 | 07:14 PM

    Ah... Tuskegee revisited...
    Anybody seen Ray Kurzweil? I'm sure this story would be more fodder in his quest for immortality. I think Benacio del Toro summed it up best in his upcoming movie....
    "I will kill all of you..."
    I concur with his astute assesment of the medical community.

    Posted by Dr. Mabuse on February 1,2010 | 07:15 PM

    Excellent article, I think the family should be compensated.

    Posted by Tinita Jones on February 1,2010 | 07:15 PM

    I agree that human cell research is invaluable to medicine. We should learn from past mistakes made concerning the rights of these persons/families and their cells. Our society attaches monetary value to almost everything in existance. Why then should our cells be any different? People who are lucky enough to have this type of cells should be able to prosper from them just as someone who has any viable product. Hopefully in the future if a person is found to have cells that could benefit our world researchers will be forth comming with this information, and families can at least be compensated for their contributions.

    Posted by J\Ivanna Sherrill on February 1,2010 | 07:15 PM

    Wow! Very interesting story.

    Posted by Julius Lara on February 1,2010 | 07:16 PM

    Great story.........I will probably buy the book.. Actually my husband died of "Brain Cancer" in 1996. I gave the doctors verbal permission to use my husband's brain or whatever parts they needed for research after his death. I never signed anything and am not sure whether or not they used any of his body parts. He had participated in several research treatments so I'm assuming he was "used" for research. How can I find out? Thanks......

    Posted by Nancy Sypniewski on February 1,2010 | 07:16 PM

    simply incredible amazing wow

    Posted by nylor jay on February 1,2010 | 07:16 PM

    JMO,,,,, but I feel that you and the family should make Millions,, thank you so much for exposeing this tragic story,,,,, maybe you can ask the A.C.L.U. to help in some way..

    Posted by cliff on February 1,2010 | 07:16 PM

    this is very interesting story and nice to know that cell tissue can used for experimental purposes.

    Posted by judy on February 1,2010 | 07:16 PM

    Fascinating article, and I will be forwarding it and getting the word out....I am distressed that it looks like it was written by a young person....the sentence structure is poor, and calling fruit flies 'inanimate objects' doesn't do the author or Mrs. Lacks any credit...I'm amazed the Smithsonian didn't vet this better.....but it will get forwarded, and I look forward to learning more.

    Posted by PJ on February 1,2010 | 07:16 PM

    Very interesting story! This also shows another instance of black people being used as guinea pigs without their consent, or approval(see the Tuskegee experiment, where black male soldiers were intentionally infected with syphilis, and never treated, or told that they were, or see the nazi medical experiments in South Africa in the 30's)

    It is time for this family to make moves for compensation for the use of their families genes without consent. I think they will win any case that they bring forward.

    Posted by black male on February 1,2010 | 07:17 PM

    Absolutely fascinating-I'm sure many people have been helped by this inadverdant giving. Thank you Henrietta Lane.

    Posted by Frayda Kerstein on February 1,2010 | 07:17 PM

    Hogwash

    Posted by Donzi on February 1,2010 | 07:17 PM

    What an incredible legacy for a young black woman that help heal a world.

    Posted by Kim on February 1,2010 | 07:17 PM

    What an incredible legacy for a young black woman that help heal a world.

    Posted by Kim on February 1,2010 | 07:17 PM

    I think it's total speculation by the above poster to assume that they did not attempt to treat her with what was available at the time. Heck, sometimes that cannot cure cervical cancer now.

    To not read the book because one has a chip on their shoulder is a disservice to this woman and her family.

    How haunting and amazing! I would be real proud if my cells were used to cure diseases like polio and launched gene mapping, etc. I think the remaining family - direct descendants only should be compensated.

    It's funny that the school nurse confused sample contamination with disease contamination in the remarks above. Well, pathetic funny anyway.

    Posted by Shelley K. on February 1,2010 | 07:17 PM

    Why assume that she is the only one whose cells have been used this way? -- without her permission! When I had ovanian surgery in the 90's, I wondered if my eggs were sent somewhere by the lab and used without my persmission. I wondered if I would someday meet my children in Heaven that I didn't even know about.

    Posted by Sharon on February 1,2010 | 07:18 PM

    I don't understand why the Lacks feel they are owed all kinds of money. It is their own fault that they are broke and homeless. They should see that their mothers cells have done a lot of good through research and have probably saved many lives. That is so much more important than money. People always trying to get paid when they did nothing to earn the money.

    Posted by Lily on February 1,2010 | 07:18 PM

    This is almost like the Marvel Comics characters Wolverine or the Incredible Hulk. They could regenerate after being hurt because their cells would grow back almost immediately. Only this woman didn't have claws or super strength (As far as we know...)

    Posted by Steven on February 1,2010 | 07:18 PM

    It's wonderful that the HeLa cells are helping people, but I also believe that Henriettas family should be compensated. The scientist took her cells for research. They definitely should have asked for permission from her husband and or family...

    Posted by JC on February 1,2010 | 07:18 PM

    Interesting article...a must read. I planning on getting the book.

    Posted by Doreen Marson on February 1,2010 | 07:18 PM

    I'm amazed. Cells that never died. It's like the saints of GOD who die and their bodies do not decompose. I can only wonder if this woman were caucasian, would the doctors have bothered to get her permission? HELA probably would have allowed it had she been asked. African American women are notoriously giving and accomodating, even at their own expense. Well, I too want to read the book. The family must be compensated financially. That is the lady's way of caring for them long after she has left at so young an age.

    Posted by BOBBIEANDSNOOKIE on February 1,2010 | 07:19 PM

    This was a rather interesting article. It calls into question our basic definition and understanding of the word "death", as most humans know or accept it.

    It suggests that human forms (bodies, cells, etc.), and probably all other life forms, may normally change or morph into new or different forms at different points. One of those major changes may occur during or at the stage we commonly call "death."

    Apparently, we have only a limited knowledge of really what happens at the "death" stage. Not fully undersanding this stage, we grieve, become sad and remorseful because the change is so dramatic and because we can no longer physically see, hear, touch, communicate with, feel, or be with the changed (dead) individual.

    The article mentioned the word "immortality." Humans seem to have a preoccupation with "immortality." This is reflected in our religious and spiritual beliefs, arts, histories, institutions and politics. It is also reflected in our constant efforts to remain youthful.

    Is it possible that all of life is immortal? Is it possible that all of life has been here forever and that it goes through millions and millions of changes,including "deaths," over millions and millons of years? Is it also possible that human understandings of all of this is contrained by human theologies, sciences, politics, histories, etc?

    Oh, there is so much to learn and so much that may not ever be known; or, it may become known over periods of millions and millions of years.

    Posted by Ralph Wheeler on February 1,2010 | 07:19 PM

    AMAZING!!! I loved reading this article...I am a high school science teacher and I think I will suggest this to my students! Wonderful!

    Posted by Tamara on February 1,2010 | 07:19 PM

    its very interesting know that this phenomenon has interest someone to research further about the issue and ended helping the family and making more people understand the importance or science. getting samples from anyone needs permission from the to be donor. scientist should also be considerate of the social and psychological effects of this issues once it goes out to public. nevertheless it was a wonderful research article... very educational...........

    Posted by clark padduyao on February 1,2010 | 07:20 PM

    Tumors are said to be immortal because they can divide as much as they want unlike the normal cells that become unable to divide after some time. Maybe I'm wrong. I'm just a 2nd year High school student so there's a great possibility that I'm wrong.

    Maybe this is the time that the immortality of tumors was first discovered.

    Posted by Ian on February 1,2010 | 07:20 PM

    Reparations for blacks are over due. When blacks invented something while enslaved the white owner took it. this family should get paid billions. And people now it.

    Posted by Bobbiemac on February 1,2010 | 07:21 PM

    if the family didn't receive the money they are owed, because of the mother's donation to an entire industry, making billions, i am not interested. tell us, did they get their due and justified compensation? all i can say is the author is totally negligent in not completing her work by telling us all the complete story. it is still a work in progress until she tells us. i will not read-buy this incomplete book until she completes her job. what's with the tease?

    Posted by daniel on February 1,2010 | 07:21 PM

    Fascinating article, and need to buy the book....but still think a documentary should be made to get the story out! The husbands version of what happened to his wife would be laughable....until you read the comments from her daughter...sad! Still think the family should be compensated!

    Posted by Beth on February 1,2010 | 07:21 PM

    Dear Posters,

    It is truly amazing how so many do not even understand medicne in the 1950's. They had very little to treat women's cancers back then. Even in the 60's treatments were not there. Chemo came into being because the military had chemicals left over and they did not want to throw them away. So they took the poisons and made cancer treatments out of them.

    I am shocked to see everyone talking about money here. Money was made after millions of dollars in investing in the research. Do you really think that they just looked at her cells, and it was a big help to curing things.
    So please realize that her cells were the raw materials that were used to start genetic research and to find cures.

    Do you realize how many folks have contributed to medical science through many different avenues. Whether it is trying a new drug, or a new procedure.

    The shock that many of you look at the money tells me where you are coming from. Heaven forbid that you should have to be paid to have some doctor do something to you in the name of Medical Science.

    Please take note, they say that Doctors have a Practice, note the word practice.

    Do the authors of other books give the money to those they write about, NO, it is called America, we are a Republic, we have Free Enterprise here.

    I am just happy that this woman has chosen to write and share the story with us. If you have the time, please read the book, The Double Helix, about Watson and Crick, the guys that cut the lady scientist out of the DNA research long ago.

    Remember, we all contribute to medical science each time we go to the doctor.

    So you money grubbing folks, not everything is about the money. Her family may have been paid $10 way back then for something that was going in the trash. They should now be proud that their mother has helped millions of others including themselves. We are all in charge of our own educations, school teach, but remember we are the one in charge of our learning.

    Posted by sal levi on February 1,2010 | 07:21 PM

    There is a lot of follow up with this article as it leads to other questions. It raises the question of legal consent of the use of these cells from the woman. The scientist took her cells and used them without her permission. And then there is the financial aspect of this as well. Money has been made from the use of these cells and this goes to the bigger issue of medical treatment of blacks during those times and that is the blatant abuse of privilege subjected against the uneducated poor class. It would be interesting to know if the medical community, who benefited from the use of these cell, compensated the family for the cells they stole from this woman. It also raises the question of who owns these cells? Was it theft by omission? Theft by proxy? Theft by depraved indifference based of the social status of the people involved? As much as the medical community has benefited in using these cells, someone has to take responsibility in using these cells without the express written consent from the family and with full compensation for the years the family has been deprived.

    Posted by Bobbie on February 1,2010 | 07:21 PM

    What a resounding story. Scientists should realize that they are affecting human lives in their desire to save human lives. Sounds complicated, huh?

    Posted by Glory on February 1,2010 | 07:21 PM

    This explotation of a fellow human being,who happens to be black,continues in a form not often viewed as explotative.That of training our future doctors in poor city hospitals using poor black folks as fodder then leaving for pastures which exclude those same folk

    Posted by Wayman on February 1,2010 | 07:21 PM

    Fascinating but controversial story about how medical research operates to make progress and billions of $$$$ at the expense of poor people.

    Posted by M. Lookout on February 1,2010 | 07:21 PM

    VERY INTERESTING! I'd like to have a copy of that book. Thank you for the information. I think the family should be compensated.This is such an amazing story.

    Posted by Cora M. (Mla.) on February 1,2010 | 07:21 PM

    I don't see why she should be entitled to compensation for cancerous tissue that was removed as part of her treatment. She should have been compensated for undergoing a procedure if the purpose had been to obtain tissue for cell culture, but apparently this was not the case. At the time, I'm sure that at the time she was glad to get these cancer cells out of her body. Any monetary value that the cells have had is the result of the risks and work of the people who recognized their use, maintained the culture, and found others who could use them.

    If she should be compensated for the cells, then she (and her heirs)should also accept the downside. Shouldn't she compensate the scientists whose other cell lines were contaminated by her cells, thus rendering them useless? Or what about the owners of animal breeding labs whose sales of lab rats and mice were diminished by the competition from the HELA cell line?

    By the way, the cells are "immortal" because they arose from a malignancy and have lost the normal signal to stop reproducing. Each individual cell does die, but not before it has produced enough offspring that are sustained by the nutrients in a lab dish to ensure that the lineage, not the individual cell, survives.

    Posted by Michael on February 1,2010 | 07:21 PM

    Am I the only one who find it a bit suspicious that nobody knew the identity of this woman until a bio teacher at a community college leaked it out? How did this person know and what was his or her source? Great story and very interesting, just seems a bit convenient that this community college instructor knew what others could not find out.

    Posted by Laurie on February 1,2010 | 07:22 PM

    The isbn # is 9780307712509 You can get ti at Barnes & Noble; amazon, etc

    Posted by EJ on February 1,2010 | 07:22 PM

    Here we go again. Instead of concentrating on the fact that this woman (who happened to be black) has helped to save millions of people. BUT NOOOOOOOOOOOO. It's the ole bs on how bad white people are. It's gettin real old and it will be sad when it all breaks out. You know what why dont we just go back in time and retake all the wealth and land the Romans stole. Better yet, why dont we go even further back and retake the all the land, wealth, and LIVES the blessed and loved Egyptians decimated during their tenure. I mean they killed and enslaved sooooooo many people (white and black) that they sold their own people into slavery. Go figure... White people, time to stop buying the hype. It is okay to be your skin color that God gave you. For everyone else, get over it!

    Posted by bulldewdew on February 1,2010 | 07:22 PM

    Very interesting. Thank you!

    Posted by Kirk Nicart - Cebu City on February 1,2010 | 07:22 PM

    I went to college late in life, in my 40's and I learned about the Hela cell in my biology class. It was in one of the information boxes in our text book. I was very fascinated by this and have never forgotten it. I have many times told someone about the Hela cell and what I had learned in class. This was a very interesting article and believe that the Hela cell has been very beneficial to science and research.

    Posted by Deanna Irwin on February 1,2010 | 07:22 PM

    This is great reading and a excellent Black History Month choice. I have been hooked, waiting on the book. The family should recieve rolletys, So now we need some Afro American lawerys to do their Pro Bono to get started. Once the settlments come , there will be fame and at least 100 million in this case. Black Homer rides agin.

    Posted by HLSII on February 1,2010 | 07:22 PM

    I would be interested in reading the book. As far as people not wanting this to turn into a racial thing, would their response be the same if the cells were from a German, Irish, Russian, Indian, ect........? Something to think about!

    Posted by Terri Miller on February 1,2010 | 07:23 PM

    A very good story has come out of all this,but any compensation due to the family, is due to her husband. And it would be worth more to help him understand what has happened and what his wifes contribution to the world was I think would be better than the money. Do you want to know how important your family is to the world, or what there worth.

    Posted by HC on February 1,2010 | 07:23 PM

    this article is very interesting..and to track the history of science wasn't an easy task..well done. i'm gonna get this book and hopefully it is available in malaysia.

    Posted by Ann Sedai on February 1,2010 | 07:24 PM

    The Henrietta Lack story is powerful! I heard of it in the early 70's as a high school student. It's amazing what has been kept from my race of people regarding contributions to this country from black americans. It makes me sad that even with the contribution my race has made to this country and it's citizens we are discriminated when it comes to politics, education and employment, but I do find comfort in knowing that when I stop at a traffic light, use a computer, watch television these items advanced due to the contribution of black inventors. It's time America's history was rewritten with blanks filled in for all to see the truth. I am fortunate to come from a family where members have lived well into their hundreds, I know my history and it's time all of America knows!

    Posted by dorothy cooks on February 1,2010 | 07:24 PM

    Her family never received any payment. They took her cells without her knowledge, they should be sued.

    Posted by maurita terry on February 1,2010 | 07:24 PM

    wow. .that cell. .only one people got that cell? no right . .there must be the other person who got a greater cell than that cell . .

    Posted by badar on February 1,2010 | 07:24 PM

    Is there any body who is powerful and have a connection to the high official that could extend thier helping hand to help the family? In God sake be kind to them..... those scientist concerned....

    Posted by lydz perez on February 1,2010 | 07:24 PM

    What a great story! Henrietta's family should be very proud. Think of the lives she may have saved by the Dr. removing the cancerous cells to have them tested. It really annoys me that people think she was harmed or done wrong by this Dr. taking these cells and that her family should be compensated. Another example of GREED.

    Posted by Steve G on February 1,2010 | 07:25 PM

    I owe a debt of gratitude to this lady! I have used these cells in my research for a ton of different things and they are used everyday to culture and identify viruses that are causing disease so that patients can be helped! She has given us a tremendous gift. And we need to look at it as just that, a gift. Today you need the consent of the person before anything can be done with anything that is taken from the person at any institution. We have Institutional Review Boards that monitor all experiments that include any part of human involvement in research. Patient consent has evolved over the years as well. These cells were not taken with any malice of forthought. Now the patient would be "consented", but this was 50 years ago. The taking of the tumor was probably to hope it would be removed and at least arrest the process for a while. And since it was going to be "discarded" their thought was why not study it to see if it could help her or others with this devastating disease. Today even "discarded" tissue has to have consent to be used. Things have progressed for sure.
    Back in the 50's there was not much that could be done for cervical cancer, but people were trying to figure it out. I'm sure that is why her tumor was used. We have come a long way since the 50s in both what we know and how we do research. Believe me I have not made "millions" from my research. In fact it is not a job I would recommend if you are interested in monetary gain, but it is rewarding to help people in any way we can to live longer and with more quailty to their lives. I am willing to "give" my knowledge and my findings to society to help them in anyway I can. And that's what places like Jonhs Hopkins University do...findings are published and knowledge gained is "free" to read and use. If someone didn't "give" their knowledge to further the efforts that these cells have been used for, there would have been no reason for this discussion. Everything isn't about money...is it?

    Posted by Karen on February 1,2010 | 07:25 PM

    What an interesting story! Just amazing....She has left a legacy for her family and a gift for the world, regardless of the cost. It would make an interesting movie and I hope her family was compensated for the contribution she made. Even though she never knew what had been attributed to her. What they have to be thankful for in return.

    Posted by Janet on February 1,2010 | 07:25 PM

    Very interisting facts. I am not very familiar with cell. Do HeLa cells unusual? Do all human cell can be grown like HeLa cells?

    Posted by Agus on February 1,2010 | 07:25 PM

    i thank her for her gift she may have saved a family member or friend,i think she should be honered with an award for her contrabution to humanity,she may not have had an education but she sure had a heart.her family should be proud.i know i would be.

    Posted by carol ann moody on February 1,2010 | 07:25 PM

    I am delighted that Rebecca had the drive to keep on until the book was completed. Some seem to miss the point that Henrietta was not advised as to the disposition of what was removed from her body nor was she asked for approval of what was being done. (How often have you had tissue removed and not advised as to the disposition? How would you or your family feel to learn the facts?) Likewise when the importance was known, no one took the effort to advise the family. Just think what a difference that would have made to them--a mother's legacy not only for them but for others. Probably she or the family would have okayed the tissue for study but that was not the situation. I, for one, believe there should be some compensation to her heirs. Did not those growing her cells just donate? I doubt it, I'm sure they sold the HeLa cells.
    If an attorney has not been retained by the family, how about one of the ambulance chasers coming forward? This probably should be a pro-bono case or the attorney can wait for his pay and expense reimbursement once the case is settled.

    Posted by Alaysia on February 1,2010 | 07:25 PM

    very interesting story, this is a little unknown Black History facts. I look forward to reading the book and sharing the story with family & friends. Thank you.

    Posted by Fannie on February 1,2010 | 07:26 PM

    This is a fascinating story! I hope the book does extremely well.

    Karen
    www.karenjordanwrites.com

    Posted by Karen Jordan on February 1,2010 | 07:26 PM

    THIS IS A GREAT STORY JUST ANOTHER STORY OF HOW THE AFRICAN AMERICAN HAS CONTRIBUTED SO MUCH TO OUR SOCIETY AND HOW IT IS KEPT SECRET BY WHITES WHO TRY TO DENY BLACKS THERE JUST DUE AND COMPENSATION JUST AS THEY HAVE DONE WITH THE FORTY ACRES AND A MULE CONCEPT GIVE US OUR DUE AS HISTORY SHOWS IT WILL ALL COME OUT IN THE WASH AS THEY SAY THE TRUTH CAN BE HIDDEN FOR ONLY SO LONG AND THE TRUTH WILL SET YOU FREE.

    Posted by l.t. harper on February 1,2010 | 07:26 PM

    I thought the story was great and needed to be brought to the forefront of what we know about where scientists find the basis for a lot of the things they do. I sincerely hope the family is compensated for their mother's contribution but I do think the answer to that question was purposely left out as a teaser to get you to buy the book.Congratulations to the Lacks Family for being such a big part of black history!!

    Posted by michelle on February 1,2010 | 07:26 PM

    This article is absolutely amazing! I am really interested and would love to know more about what happened to the family and more about how her cells impacted modern science. What would that mean if her offspring shared her same cells? Then what does that mean for cell research and vaccines?

    Posted by n from jersey on February 1,2010 | 07:27 PM

    i learned about this

    Posted by Aly on February 1,2010 | 07:27 PM

    They should collect Social Security benefits for her since she is still alive.

    Posted by radtek2112 on February 1,2010 | 07:27 PM

    This sounds like an Oprah book club or a movie mini series.

    Posted by Dennis Horton on February 1,2010 | 07:27 PM

    >>Racist or not, taking someone's tissue without out their permission or knowledge and not informing the family is pretty sneaky and border line malicious.

    You guys don't undersztand how this works. Taking such tissue did no damage to her (not the least because she was dying already) and he probably only took a few slivers.

    We have enough frivolous lawsuits as it is without someone making up a new one because of something that happened decades ago.

    Posted by Caroline Miniscule on February 1,2010 | 07:28 PM

    Amazing!! I have a mutated gene of NF and so do some of my children and grandchildren. Didn't know anything much about this disease until a few years ago when they isolated the gene. There is no cure. It comes out in tumors, inside and outside the body which grow along on the nerve endings. They can become cancerous.

    Posted by Kathy Shaw on February 1,2010 | 07:28 PM

    Im wondering if the doctor didnt take her cells because of the cancer not cause she was black - maybe he took lots of cancer cells- it said no other cells had lived before hers-what ever the reason- good thing for us today that he did and that cells are helping us. I want to read the book!!!

    Posted by lorik on February 1,2010 | 07:28 PM

    Interesting revelation. I hope we can download it somewhere here. thanks!

    Posted by mark on February 1,2010 | 07:28 PM

    This is very interesting I really did not know that, thanks so much for the info and your research. Now we should have someone else to celebrate in February for Black History.

    Posted by Linnie Heard on February 1,2010 | 07:28 PM

    Interesting what? cell grows.It is not immortal.It does not fascinate me at all.

    Posted by zainal othman on February 1,2010 | 07:28 PM

    I can almost understand this story because my nephew passed away and it was hard for my sister to make a choice to give up his body parts because he was so young and it being her baby boy ,it was a tough decision ,but we do understand it helps to save other life.sincerely

    Posted by Aneina on February 1,2010 | 07:28 PM

    This synopsis of a great biologycal miracle only proves that there is more to life than just what we see. Science still has a long way to go to find the cure for many ailments and the answers to many unanswered questions. However, I do hope that when samples of human tissue are taken for research the families are notified,consent forms are sign and that the only ones to benefit from it is humanity as a whole. We have no right to financially profit from those who are unaware of the mysteries of science.

    Posted by AMBRR on February 1,2010 | 07:28 PM

    if true, this is all very wonderful, but how is it that she died if her cells were immortal?

    Posted by kennon on February 1,2010 | 07:29 PM

    Amazing and interesting.

    Posted by Ronald Von D. Rivera on February 1,2010 | 07:29 PM

    Obviously most people do not realize this, but in the US once tissues such as tumors are removed from your body they are consdered autonomous and no longer yours. This is also true in most other countries doing a significant amount of research into cures for cancer, chronic diseases, or even antioxidants in food. The difference today is that due to privacy laws scientists would make sure the cells could not be traced back to Lacks. For all the research done, I think the writer could have looked more closely into the laws instead of implying this was some immoral thing done only to poor black people, which I fin. Before you start crying foul about scientists making money off your tissues, consider if every scientist had to pay a person and their descendants royalties to use cells for treatments. Imagine if treatments for your cancer of the spleen were not available, simply because the man whose tumor cells they were developed from (or their descendants), who did nothing but allow the tumor to be removed, wanted to charge too much money, would only sell to the highest bidder, or decided not to allow them to be used anymore one day?

    Posted by Research Tech on February 1,2010 | 07:29 PM

    I find it interesting that there are so many "concerned" that claim something is owed. What was standard practice back then (sharing sick tissue for research) did not require permission. AND,consider that the cells were going to be tossed into the garbage can anyway.

    The only ones that benefited from this are EVERYONE ALIVE TODAY, INCLUDING THOSE THAT ARE COMPLAINING...If you feel that the children are owed, I suggest that you contact them and pay your part of the debt...Let me know how that goes.

    Some people are all about what they are owed, not what they can do to help.

    Henrietta, please accept our thanks on Earth and our prayer that you received your reward in Heaven.

    Posted by John Houston on February 1,2010 | 07:30 PM

    according to the principle, things are not created neither destroyed, only they´re changing.

    Posted by chuck on February 1,2010 | 07:30 PM

    Thank you for your wonderful job; I can not wait to buy the book.

    Posted by Joseph Nsiesi on February 1,2010 | 07:30 PM

    Very intresting, I would love to read more about her. Truly amazing !!! her family deserves the best.

    Posted by Armida on February 1,2010 | 07:30 PM

    This is a great article. I learned something new and gained a new interest in how cells are used to help mankind and learned tid bits of a family. This article does generate interest in getting the book to read the whole story. After reading comments above, I must say, please look at the "by Line". This isnt the whole story. The author of this article basically interviewed the author of the book. These were the questions the author answered. If you want to know the whole story by her account then purchase the book. Everyone wants to know if the family was compensated, yes, and everyone wants to know more, that is a given. But dont bash the author of the article or the author of the book for not disclosing everything in the book.
    I am thankful for the research and for Mrs. Lacks for me, my family and everyone else that has benefited. "Back in the day.." they didnt do as we do today. It was unfortunate that she wasnt asked or even knew about this being done, but that was a different time. IF you feel that it isnt being handled correctly in THIS day and age, then do something about it. If you feel it was about race then please come back to TODAY! Yes back then it may very well have been, but please dont use someones life story from the 1950's as your soap box for todays issues.
    I thought this article to be informing and caught my attention so that YES I do want to know "the rest of the story" and I will be purchasing. I want to wish the family the very best and to say thank you, this is a legacy that is unmatched. And I want to thank the author for bring Mrs, Lacks story to us.

    Posted by Mary on February 1,2010 | 07:30 PM

    This is very fascinating, really intrigued.

    Posted by Michelle Chan on February 1,2010 | 07:30 PM

    Fascinating story, though I don't agree that we need vaccines. We should be looking at homeopathy and other treatments.

    There are also some connections to my life. I was born in 1951 and of course had the polio vaccine in the 50s. I just did a clearing of that vaccine with homeopathics. After rupturing and being surgically removed, my mother's appendix was sent to Johns Hopkins around 1941; she always said it was because of its size. Now I wonder.

    It leaves me with many questions, one being what was different about Henrietta's cells? If hers were the first immortal ones, have there been any others since?

    Posted by susan on February 1,2010 | 07:30 PM

    amazing..it gives feedback about the vitality of human lifes it is also important that we know our rights.we are not animals to be tested we have feelings.

    Posted by gracie on February 1,2010 | 07:30 PM

    i loved this story i am an future fornisc patholgist this isvery help ful to kno

    Posted by richola on February 1,2010 | 07:30 PM

    Who are these people screaming racism and for compensation for the family? Please, this was the 1950's and I have a pretty good idea that cells were harvested from a lot of people including whites. We all lose cells from our body daily. Cells taken from your body for testing are no longer yours. They are usually thrown in the garbage afterward. Just so happens her timing and location were just right and the cells were diverted to an experiment and it just so happens that her cells were the lucky break the scientists were looking for. People weren't so avaricious back then....except for (according to some the posters)white folks, greedy doctors and the pharmaceutical companies. Wow, America is really going downhill fast.

    Posted by Bento on February 1,2010 | 07:30 PM

    I 'm glad I to wish to study this I think I 'am close to something but it makes me scare for people might turn it into something bad....Yes its a cure but........

    Posted by hearlight33 on February 1,2010 | 07:30 PM

    I am a 16 year old student as well,and this story was amazing.you can tell with the amount of details that this took a lots of time and effort...........i will be following on by buying the book.

    Posted by eliana on February 1,2010 | 07:31 PM

    Keep up the search! there is so much more to this story and to the lady that the studies were done on/from. We will never know the whole truth to our bodies, that's not for us to know, BUT! we can use it for our destiny. You can not change DNA, BUT you can alter it!

    Posted by tls on February 1,2010 | 07:31 PM

    As the story goes,what goes around comes around. Those who are last shall be first and those who are first shall be last!!!!!I believe that she is a blessing for all man kind and I also believe that those scientists hadn't planned on this to come out like this,or to come out at all.That's why I'm so please that we have BLACK HISTORY month.I believe that all people have a gift for something.I also believe that things are there all we have to do is just bring those things into existing. God is all and through him anything is possible. That's why a CHANCE has come and there are things yet to be seen.

    Posted by Lora Ealy on February 1,2010 | 07:31 PM

    Thats pretty cool! I can't believe her cells are still alive. I'm studying science and that is a very interesting topic. They were able to do so many cool things with those cells. They cured Polio!! That is really cool.

    As for the family, they should just be proud that she was able to contribute to so many years of health like that. They should maybe get a little compensation but I have to agree with the comments here- what did they do to earn any of the money? Just because you are poor doesn't give you the right to think the world owes you something. People have money for a reason - they work hard! Few people are handed money in life they must work hard for it. If you are poor maybe you should have worked harder, but it does depend on your circumstances.

    Posted by sabrina on February 1,2010 | 07:31 PM

    "It turned out that HeLa cells could float on dust particles in the air and travel on unwashed hands and contaminate other cultures." This makes me wonder if it is possible to spread cancer from one person to another in this manner.

    Posted by Jim on February 1,2010 | 07:31 PM

    WOW! This is amazing! I loved the article, will buy this book! The only thing that disappointed me was the fact that too many people were only concerned with a money issue! If that was any part of my family I would leave the money issue alone! Who cares about almighty money in a case like HeLa cells! If cells can be immortal that might mean other parts of the human can be immortal also. Am I correct?

    Posted by Violetta Flower on February 1,2010 | 07:31 PM

    This is a very interesting story. I would be surprised if a movie or a documentary film was done on this story. Many of times people forget what it takes to make these cures or the research that it takes to get even close to a cure. No doubt taking the cells from Mrs. Henrietta Lacks without her permission was wrong. A lot of the above comments pretty much demanded some type of conpensation. If we conpensated everyone on everything that we did for research, we would not have the technology that we have today. An enormous amout of money is spent on research before we find a cure. I hope the family of Mrs. Henrietta Lacks understands what Henrietta did for the world. With her cells, she has touched many areas of research. With God's Blessing Henrietta with touch and save many lives. I wish her family well and good blessings come their way.

    Posted by Joe Broadus on February 1,2010 | 07:31 PM

    In a society that is still struggling with race and equality, I wonder how many people over the years have been touched by a gift for humanity from a long deceased poor black woman who lived and died during a time when she was considered a second class citizen. Without ever knowing it, Henrietta has saved and will save countless lives all over the world.

    Posted by J.A. Duncan on February 1,2010 | 07:31 PM

    Many of you need to read a little about immortal cells because you seem to have the wrong impression of what they are. Its not your fault to get these conclusion as the author did not makes this very clear.

    Posted by K on February 1,2010 | 07:31 PM

    it is a fascinating story. however, i don't understand why the family should be financially compensated.

    Posted by nicole on February 1,2010 | 07:31 PM

    While HeLa cells created a "multi-billion dollar industry," it's sad to know HeLa's family and descendants are living in the gutters because of poverty. I agree with everybody above who said the family should get something, at least financial, from HeLa cells. For science it's a great discovery!!!

    Posted by Ragg B. de Rojas on February 1,2010 | 07:31 PM

    very interesting story..

    Posted by godfrey on February 1,2010 | 07:31 PM

    Cell and blood are for the life of the body not the life of the soul some cells from this womans body may still be living under Ideal conditions but eventually will die probably around 120 to 125 years from the time of her birth . That is coming from a Biblical standpoint 17th chapter of the book of Leviticus.It is wonderful that doctors can try to find cures for illness.But I think they should only be used for the purpose of helping the living.

    Posted by shawn on February 1,2010 | 07:33 PM

    very interesting , please let me know when other information comes out . please give me the info on the book

    Posted by Regina Taylor on February 1,2010 | 07:33 PM

    The family was deceived and taken advantage of because they lived circa, 1950's. One of the most racist times in American history. Look at what her cells have done for research. The family should receieve at lease a billion dollar compensation from what her cells have done for science and the multi-billion dollar drug industry.

    Posted by Michael on February 1,2010 | 07:33 PM

    I will definately buy the book. Cant wait to read more about this.

    Posted by Tabitha on February 1,2010 | 07:34 PM

    Great read! I remember studying about HeLa cells in biology in the early 60's but NEVER gave it a thought that they actually came from any one specific person. How dumb could I have been! May God Bless the family of Henrietta.

    Posted by Linda Hayes on February 1,2010 | 07:34 PM

    One of this cells might be used to create a clone..

    Posted by on February 1,2010 | 07:34 PM

    Sorry, but I just don't buy it.

    Posted by Elsa on February 1,2010 | 07:34 PM

    Amazing. All I can say is I will definitely by the book.

    Posted by Yolanda on February 1,2010 | 07:34 PM

    What compensation?
    The question is, did the doc do everything in his power to save this woman's life or spare her unnecessary suffering?
    If he did, then it's fine and that's the end of the story.
    The swab he took from her cervix was useless to Henrieta Lacks or her family (as much as the tissue I blew my nose in yesterday is useless to me).
    The fact that Henrietta's cells went on to help science is something she would probably be proud of. She was not there to see her children grow, but I think she'd be glad to know her short life helped not only her children and grandchildren, but and millions of others as well.
    That's the thought that prompts so many people to become blood and organ donors.
    I mean if it's no use to you, why not let it be used by others?
    As for the scientists, when selling Henrietta Lacks cells, they actually sold their work in preparing/culturing/etc those cells. I don't think Mrs Lacks (or anyone) would have gotten much for selling them in their natural state.

    Posted by maria on February 1,2010 | 07:35 PM

    HOW COULD A DOCTOR DO SUCH THING. A DOCTOR SHOULD BE HONEST AND TRUSTWORTHY. HE SHOULD HAVE TAKEN THE CONSENT OF HIS PATIENT BEFORE TAKING AND USING THE TISSUE SAMPLE OF THE PATIENT. THIS IS INDEED A VERY GOOD EXAMPLE OF DECEPTION, USING HIS BEING A DOCTOR TO A PATIENT.

    THERE MUST BE A REPARATION FOR WHAT HAVE BEEN DONE TO THE PATIENT AND TO THE FAMILY. THE TISSUE SAMPLE HAVE BEEN USED AND STILL BEING USED AND WILL BE USED FROM GENERATION TO GENERATION. THESE GROUP OF SCIENTIST OR DOCTORS OR COMPANIES WHO TOOK ADVANTAGE OF THE INNOCENT PEOPLE SHOULD IMMEDIATELY DO SOMETHING TO PAYBACK THE FAMILY OF HELA.

    Posted by CAROL on February 1,2010 | 07:35 PM

    woooow!!!!! not that i can't read, but book reading 4 pleasure or fun is da least thing i'll do , but i'm going to have to buy this book bcuz it's really got my attention!!!!!

    Posted by Arthur Smith on February 1,2010 | 07:35 PM

    Amazing!! Found more info at http://en.wikipedia.org/wiki/HeLa Apparently the California Supreme Court ruled against the family. They need to take this up all the way to the supreme court. We need some good lawyers to take this up for the family.

    Posted by FTK on February 1,2010 | 07:35 PM

    AWESOME STORY. ...ANOTHER GREAT STORY FOR MY GRANDCHILDREN FOR AMERICAN HISTORY AND BLACK HISTORY. I WILL BE READING MORE ABOUT THIS BLACK WOMAN AND EMAILING THIS TO OTHERS. ONE MORE INSPIRATION FOR ME, A CANCER SURVIVOR..... THANK YOU HENRIETTA..... FOR YOUR CONTRIBUTION IS GREAT..HER FAMILY SHOULD BE CONPENSATED. THIS WAS DONE WITHOUT THEIR KNOWLEDGE AND HELPED SO MUCH. THE DRUG COMPANIES MAKE BILLIONS. WHAT THIS FAMILY GETS...IF THEY DO... WOULD NEVER BE EQUAL IN VALUE TO THE CONTRIBUTION THIS WOMAN MADE..

    Posted by p coleman on February 1,2010 | 07:35 PM

    These immortal cell lines are called "continous" and HeLa cells arent the only ones available. I imagine whoever figures out why they are immortal would receive the Nobel Prize. I actually use a cell line which came from a girl fetus who died in the early 1960's. Although not "immortal" like a cancer cell line, they are repeatedly duplicated.
    Excellent article; wish it would have mentioned what he policy is today for tissues and cord bloods which would normally be thrown away but used for research.

    Posted by Roberta on February 1,2010 | 07:36 PM

    How and why was this kept quiet so long? The ethical behavior of the research team clearly reflected the ethics of that period of time. Do other members of the family have the "immortal cell ".

    Posted by Herb Fraser on February 1,2010 | 07:36 PM

    Amazing story.

    Posted by Dorothy on February 1,2010 | 07:36 PM

    Great piece!! Life is a life and doesn't distinguish beteween color, race or religion. Something of a higher power gave the knowledge and instinct to research and find cures or treatment for illness. Henrietta was on this earth to provide such for the rest of us to benifit from. Maybe and hopefully, her family are also a rare and gift to all of us who could or would suffer from an illness. To anyone who has endured medical and finacial dispair, I can only hope that they reap what should be awarded to them both financialy and mentally. I also hope that the legasy be passed in the family name to insure that all is aware of who and where Henrietta came from.

    Posted by jan lasater on February 1,2010 | 07:36 PM

    THE STORY WAS BOTH EDUCATIONAL AND INTERESTING. IT'S CRAZY HOW THE HUMAN BODY WORK AND HOW ONE WOMAN COULD HELP SO MANY. I'M GLAD YOU TRACKED THE FAMILY DOWN AND THEY GOT SOME KIND OF ANSWERS THAT THEY WEREN'T AWARE ABOUT.

    Posted by ANGEE on February 1,2010 | 07:36 PM

    yes i would have to agree that this is a very interesting story, but for all the people singing the praises of this story, to me it just smacks of what the government did to the blacks of tuskegee, ala. and the V.D. "testing" i guess back then the so-called doctors thought it was ok to experiment on black people and not pay them or let them know what was really going on....

    Posted by david on February 1,2010 | 07:36 PM

    This is an amazing story...I've definitly have to get the book!

    Posted by Jania Luave on February 1,2010 | 07:37 PM

    Since many Americans receive polio vaccines, is it possible that the immortal highly contaminating HeLa cells taken from a patient’s cervical cancer tumor, develop into cancer in people receiving those cells or by products of those cells? Is it possible that HeLa cells which have many uses and are found in many cell cultures are causing breast and prostate cancer?

    Henrietta’s cells were the first immortal human cells ever grown in culture. They were essential to developing the polio vaccine. Many scientific landmarks since then have used her cells, including cloning, gene mapping and in vitro fertilization.

    Twenty-five years after Henrietta died, a scientist discovered that many cell cultures thought to be from other tissue types, including breast and prostate cells, were in fact HeLa cells. It turned out that HeLa cells could float on dust particles in the air and travel on unwashed hands and contaminate other cultures. It became an enormous controversy.”

    Posted by george brown on February 1,2010 | 07:37 PM

    Pretty cool how just a street smart women could help teach a whole bunch of highly educated people somthing and would become famous which she deserves. This happens all the time now with no big pay outs. She got to be a pioneer in somthing important without even knowing. Died too young but will live in are history and future for every. I do not beleave the doctor was a evil racist thinking he was going to make a trillion dolars on a tumor, No telling how much researchers spend on there research and sometimes it probaly feels like it going no where, I think the doctor was just being a doctor interrested in his research progress. As long as she got as much attention from the doctor when she was alive, I think thats whats important.

    Posted by DAVID on February 1,2010 | 07:37 PM

    I like the closing paragraph, which is ... to see everything in a Positive View. "...Instead of saying we don’t want that to happen, we just need to look at how it can happen in a way that everyone is OK with...." BUDI R @ http://twitter.com/budi_rachmat

    Posted by Budi Rachmat on February 1,2010 | 07:37 PM

    Very interesting story. Sad to hear of someone dying so young.

    Posted by Egly Garcia on February 1,2010 | 07:37 PM

    There are a great many people living and dead that have contributed both knowing and unknowing to advances in medical science. In this past tumor tissues were used frequenrly in experimentation. generally no one is paid for the tissue they contribute. Should we collect from the accident victim if we contribute the unit of blood that saved their life? I'm sorry Henrietta's family was not as successful in life as others. I wish them the best in the future. Maybe their mother's cell line can save one of their lives some day also.

    Posted by Al on February 1,2010 | 07:37 PM

    i want to know more

    Posted by eli on February 1,2010 | 07:37 PM

    This article caught my attention. I really makes you wonder how advance science is in relations to cures. I'm totally interest in reading the whole book. Great job.

    Posted by Judy on February 1,2010 | 07:38 PM

    No one can say for certain what the motives of the scientists were, but few of them are ever in it for the money. They sincerely want to help mankind, at least at the beginning (very few of them ever discover "the cure" for anything). So for those of you who are appalled by what you term "greed," remember that but for their motivations, whatever they may have been (fame, personal satisfaction, job security, altruism, and maybe money), millions would have died of polio, and their children would have been parentless. who would have owned those children money if their parents could have been cured, but weren't? THANK GOD for the brilliant, hardworking doctors and scientists who continually strive to find cures, treatments, and vaccinations so that we can all live a little better. And for those of you who think every helper in the process should be paid, pay the scientists, and the teachers who inspired them, more, not the donor of the unwanted body part. Can you imagine how much more health care would cost if every item that was part of the research process had to be paid for relative to th value of its ultimate contribution? GOOD HEAVENS! Should a polio vaccine really cost $1000? Besides, the Supreme Court has held that once your body parts are not inside you, you no longer own them. If you dont want them used in science, keep them to yourself.

    Posted by kathy on February 1,2010 | 07:38 PM

    If scientists understand why Henrietta's cells are able to multiply indefinitely then maybe they will better understand why African-American people often don't look their true age. You could look at a healthy African-American woman who is 55 and think she's only 30.

    Posted by November Topaz on February 1,2010 | 07:38 PM

    I feel a sense of pride when I read this article. To know that a black woman has been the vehicle for such medical breakthroughs is... soul soothing. I come from a family with a history of cancers on both sides. My Daddy passed away from cancer along with his little sister, and a number of my cousins. As for the race issue... it's there and should not be ignored or passed off as just "the way it was". The truth of the matter is things of this nature still happen. I'm from the South but this racism can be find planet wide. I digress. I am looking forward to running down to Barnes and Nobles and picking this book up. Great article and wonderful topic. If any this work of truth interests you I think you should check out the trilogy Lilith's Brood by Octavia Butler. The similarities to this womans story and the character of Lilith are scary.

    Posted by A. Washington on February 1,2010 | 07:38 PM

    Interesting story. I pray that the family earned some money. This reminds me of the Tuskegee Experiment that was done on poor black farmers who where being injected with syphillis. Sad, but yet her cells have helped so many people. I hope that his book sells makes a good profit.

    Posted by L. L. Hollingsworth on February 1,2010 | 07:38 PM

    I noticed that ever since Henrietta’s cells went up in the first space missions to see what would happen to cells in zero gravity, that Many scientific landmarks since then have used her cells, including cloning....... does this mean that their is a clone of her walking around here on earth today???

    Posted by chris on February 1,2010 | 07:39 PM

    Excellent piece of collection!!pretty interesting to learn how a cell is fascinating scientists and research world. The story line up was good all the way except those part of narrow minded briefing on black on white.Let me be clear belong to neither.I question why people always become judgmental and end up with racism.Such small stories can also be portrayed as a cause of love spread the word.There werent any GCP ICH guidelines formulated in 1950's.But many common men contributed to medicine by way of participating.Its a learning experience and study.Knowledge is mans divine.Divinity is attained in any ways.So please do not use the words inappropriately because you the word.I sincerely thank the author for his efforts to bring such a point to light.Now the era begins!!Man can be immortable irrespective of black or white.Research researches to this question how?

    Posted by kik on February 1,2010 | 07:39 PM

    shocking story is that true

    Posted by John Paul Bautista on February 1,2010 | 07:39 PM

    This is just fascinating. I hope the good of this type of work keeps happening. It needs to if we are ever going to conquer the various illnesses that plague us.

    But what people need to understand is that at the time that this occured, people of color were treated less than nothing. She wasn't valued. Her rights didn't matter just like the Tuskeegee Experiments that ended in the early 70s.

    That is the reason that some people of color are very mistrustful of medicine and doctors in general.

    What is amazing is that some of the people that receive various treatments based on Mrs. Lake's cells would nearly choke or deny themselves treatment if they knew that base treatment was from a woman of color.

    Posted by lynne j on February 1,2010 | 07:39 PM

    Amazing story. I've been glued to the various versions of this story on different news web sites, and I find this story just fascinating. Very futuristic, but occurring in our past!

    What's even more interesting is that they don't know WHY the HeLa cells would continue to grow, and I quote from above.."scientists there who had been trying to grow tissues in culture for decades without success. No one knows why, but her cells never died."

    I hope they find out what was the difference in all those decades of testing then all of the sudden HeLa cells continued growing. Simply amazing.

    I think this will be a wonderful book after reading this very informative article

    Posted by spark on February 1,2010 | 07:39 PM

    About a year ago a young black man ask me if black women had given anything beneficial to science in America. I believe i found one black female scientist. Now i find one black woman who has give a part of herself to science and how her contribution has had such and impact on cancer and cell research i am proud to know that this information is now public.

    Posted by Ell Cole on February 1,2010 | 07:39 PM

    really interesting topic. If I have time, I am sure I will look for the book.

    Posted by Cindy on February 1,2010 | 07:39 PM

    Thank you for caring - I want to learn more and will be buying the book

    Posted by gardengirl12 on February 1,2010 | 07:39 PM

    I am not surprised that her cells were taken without her consent. Historically so many things have been taken from people of color by the predominant culture or race (white) in this country and throughout the world, knowingly and unknowingly, and the fact that this happened during the 50s. I've printed out this story so that I can further teach my children that African-Americans and other people of color contributed significantly to this country and hopefully they can use this story and others to assist in them becoming proud of who they are and know that they matter especially when they are confronted on a daily basis by the media and other interactions with people that they don't really matter. Just because things aren't so in your face today as it was during my mother's time and her mother's time and back and back and back still doesn't mean that it doesn't exist in another form. The actions of those doctors with the cells, the deception of the Tuskegee Experiment, what was done to the Native Americans with the blankets infected with smallpox and deliberate use of alcohol to conquer them is one of the reasons why people of color (not just blacks) have so much mistrust of whites in general and the medical community. The power base in this country is white run though it is changing and hopefully things can equal out where ALL people are counted and can feel that they matter in the grand scheme of things.

    Posted by B. McElvaine on February 1,2010 | 07:40 PM

    Mind blowing. Beginning to end. All aspects. Great job. Great work. Congratulations. And thank you to the Lacks family. Yes I do believe they deserve compensation.

    Posted by Brad Edwards on February 1,2010 | 07:40 PM

    I just knew this only now that HeLa cells is from a name of a woman...Im a med tech and im practicing it now but during my college days,nobody tell a story bout this HeLa cells..this is a good story of where things came from..fascinating and interesting story..I hope this is true.

    Posted by Luiza on February 1,2010 | 07:40 PM

    This is an amazing story, however, minorities have always and continue to be manipulated by white scientists HeLa cells lived to prove just how much Black people have been deceived throughout history and now. Scientist should have made sure her family was compensated for the use of HeLa cells.

    Posted by Patricia on February 1,2010 | 07:40 PM

    A preposition is a horrible thing to end a "professional" literary piece with. (intentionally placed here) In the minds of those in whom grammar was painstakingly implanted, it undermines the credibility of the entire piece.

    Posted by Keith on February 1,2010 | 07:40 PM

    It is very interesting to me that several people think that the family should be compensated. Why? The doctors did all the work. It wasn't like an oil well or something.

    Posted by Keith Ledbetter on February 1,2010 | 07:40 PM

    This is a remarkable and interesting story. Hoever,I do not understand why her family feels they should be made rich for something they had nothing to do with. At the time this happened, cells were also being taken from many other people. Should we try to track down thousnds of people so they can be compensated, too? The doctor didn't kill this woman to get her cells. One comment was, "This woman was beautiful inside and out." She didn't know anything about it so how can she be beatified. It makes a great story but her family didn't do anything to get money for.
    Opinion? No, reality.

    Posted by Sus Del on February 1,2010 | 07:40 PM

    the only thing different about this story is it made it to the internet. Contrary to popular belief life is a group effort not a contest as the privileged believe. Just imagine how much vital information has been lost by allowing the poor to die in the streets and in wars.

    Posted by robert palmer on February 1,2010 | 07:41 PM

    The original cells were tumor cells. Doesn't it strike anyone as odd that they were used in so many different research areas, and allowed to contaminate other cell cultures? Weren't they abnormal or cancerous?

    Posted by Ann on February 1,2010 | 07:41 PM

    IT IS SO AWESOME TO HEAR SOME POSITIVE INFORMATION THAT WAS A POSITION CONTRIBUTION TO THE AFRO-AMERICAN RACE. I TOO, HOPE THE FAMILY WAS COMPENSATED FOR THIER RELATIVES CELL AND I ALSO HOPE THEY APPRECIATE HOW THIS CONTRIBUTION HELP TO FURTHER RESEARCH FOR GENERATIONS TO COME. WE, MANKIND, ARE THE BETTER FOR IT. MAY THE FAMIY ALWAY BE THANKED FOR SHARING THIS WITH THE WORLD. THEY SHOULD BE AWFUL PROUD, I AM.

    Posted by MARY SUMROW on February 1,2010 | 07:42 PM

    HeLa cells: the cells that keep on giving, contaminating and creating new diseases so scientists and doctors can charge you to cure.

    Are Vaccines Causing More Disease Than They are Curing?
    "In the late 1960s when widespread HeLa cell contamination problems were uncovered, scientists were shocked and embarrassed to learn that millions of dollars worth of published cancer experiments were ruined. "Liver cells" and "monkey cells" that were used in cancer experiments turned out to be Henrietta's cancer cells in disguise. Benign cells that supposedly "spontaneously transformed" into malignant cells were found to be cells contaminated with cancerous HeLa cells."
    http://curezone.com/art/read.asp?ID=12&db=12&C0=735

    Posted by CancerMakesPharmaLotsOMoney on February 1,2010 | 07:42 PM

    Great!Interesting! and Amazing story! This is my first time to hear this kind of story of a human. Is it originally comes from there genes?

    Posted by rougie on February 1,2010 | 07:42 PM

    A very beautiful story. Iam 69 years old and this is the first I ever heard of this but this is natural.Now,I would just love to know more.Being that this is February,Black History Month,perhaps, more will come out about it.

    Posted by tony anderson on February 1,2010 | 07:42 PM

    How are the cells immortal if its only been recorded since 1951?That means the cells have lived 60 years not eternity.The family should be satisfied to have made a contribution to the scientific community,no one knew the cells would live this long when the samples were taken.In this month of black history this only furthers the ideal of the age of entitlements for blacks even if they actually did nothing at all.Slavery for blacks in America is over,after all most blacks who were share croppers were given 40 acres and a mule once slavery was abolished.That doesn't mean every black for the rest of time should receive reparations.End the age of entitlements and start an age of responsibility.

    Posted by JR on February 1,2010 | 07:43 PM

    So far I have not been able to find any information confirming that the Lacks family has received any compensation. In fact, there have been other cases where the tissue donors have not been compensated even when patents or cures were developed from the samples generating billions of dollars for the researchers. This topic is not going away.

    Posted by Emily on February 1,2010 | 07:43 PM

    alive since 1951 ? and the brains don't know why ?? Heck it's because they are cancer cells which are mutated and not per sae normal living cells ,yet they thrive because of the mutation !! find the mutation code that keeps it alive and WAM instant longevity..stupid science

    Posted by TOM on February 1,2010 | 07:43 PM

    First of all I think it was great research it was a shame she had to die at such a young age she was beautiful and I am sure her family missed her dearly.
    I don't think any of her family deserves payment for anything and there are alot of diffrent kinds of people out there that thinks the world owes them and they should not have to work to get it I say get a job don't blame your having to live in the streets on others.
    Do they not think that there are alot of things taken from sick people now a days that you know they are not being told they would be used for research to help in the future and that to me should be ok.
    I think if anyone thought it would help their great great grandchild if they were sick they would say yes do all you can to help them.
    (Judy Pearce)

    Posted by Judy Pearce on February 1,2010 | 07:43 PM

    It's an amazing/very interesting revelation. The family deserve some kind of grant, considering the innovatory contribution of the woman’s cell to medical development.

    Posted by Kester T. I. on February 1,2010 | 07:44 PM

    I think it's blessing that they took the cells for research. She'd be happy. But they do owe the family something.

    Posted by catrinastokes on February 1,2010 | 07:44 PM

    Fascinating information. How tragic that such a beautiful young woman was struck down so early in life! Sorry for the family's impoverished circumstances, but I don't think anyone owes them a penny. Someone invested many $$$$ to study and research the HeLa line, and the countless hours scientists have toiled over these cells to come up with truly brilliant and innovative techniques have nothing to do with input from Henrietta's family members. I would gladly donate my own DNA free of charge, and without claims to future compensation, if I knew it could benefit others.

    Posted by Karen on February 1,2010 | 07:44 PM

    What would her sons done with a piece of cancerous tissue? It is the scientist's knowledge that made those cells invaluable to more learned scientists.

    Posted by Shirley Roberts on February 1,2010 | 07:44 PM

    It is an historical fact that America's Black population was targeted for experiments. There is not proof that these scientist required or got permission to harvest cell of this patient. Yes! There should be compensation and permission from the surviving children to continue to use Mrs. Lacks tissue. Wheather the compensation be in a foundation,scholarships, or procceds from this book we are all so eager to purchase and read. I thank you for informing the public about this "HIDDEN" secret. I hope that if you or any one else write a book about this, that it will win a prize for your research and enlightenment. Richard I agree with all that you have written/commented. This hits deep within my being. I have never been touched so deeply in the past 30 years. Every thing else about Black history has been just that, "HIS STORY". I want to know more about the reacher as a member of the medical field. I'm sure it's very interesting. The cells should be archived and pattened!

    Posted by Deborah on February 1,2010 | 07:44 PM

    The story, is just a story it was edited a thousand times to make it yummier and interesting....why people get intimidated or get interested when people behind it....suffers pain...

    Posted by john paul bautista on February 1,2010 | 07:45 PM

    This is a astounding story. Na Wa Ho!!!

    Posted by ralph on February 1,2010 | 07:45 PM

    Although it is fascinating and important to world of research it is also a story that reflects some of many reasons for distrust with in minority communities. If anything the beauty of the cells exponential character is a testament to the truth, that it will not be coveted or kept in hiding. It will eventually surface and accountability for a society will be required to not duplicate such personal disrespect. A body to some may be a Petri dish to play and frolic with like a child at recess, but to others is the one thing we own and are charged to care for. And you will need permission from its owner before you run off with a part of it. It's not a commodity in the marketplace. It is a manifestation of life on earth worthy to be respected.

    Posted by Gabriel on February 1,2010 | 07:45 PM

    do you have any idea how much controversy this has probably created? You take this story and put it together with the incident that happened in the 1980's during the Reagan administation in Atlanta Georgia... You get where I'm going with this line of thinking?... The incident I am talking about is where about 25 or 30 black males came up murdered in Atlanta....It has been said that the men and boys where delibertly murdered because of some kind of chemical that could only be found in a young black male's brain that could possibly cure cancer...and now you have the controversy of American citizens trying to illegally get black haitian children out of haiti....It's too many coincidences for me..and let us not forget the incident many years ago of black men getting syphillus and being denied care or they were also delibertly being infected..I dare someone out there to give me a good reason why I shouldn't be thinking this way....it's too many vaiables to be just simple happenstance....

    Posted by pookie on February 1,2010 | 07:46 PM

    This story was told in Readers Digest at least 30 years ago and was condensed from another publication at that time because most of the Russian medical samples at the time had been overgrown with HeLa cells. Interesting but old news. Even a good story, but no one was interested that much at the time. Kind of like a musical cover of an old tune today.

    Posted by A on February 1,2010 | 07:46 PM

    What an amazing article! I was totally entrigued. I would like to read the book.

    Posted by Bridgette on February 1,2010 | 07:46 PM

    GOOD JOB! ALL IS WELL

    Posted by SEUN on February 1,2010 | 07:46 PM

    There is another very interesting book on Hela cells. The title of the book is "Conspiracy of Cells: One Woman's Immortal Legacy and the Medical Scandal It Caused" .

    Posted by shoma on February 1,2010 | 07:46 PM

    I found this article very interesting. However, I dont know why we are using diseased cells for research. Should we be using healthy ones?

    Posted by Brian on February 1,2010 | 07:46 PM

    Asolutely brilliant!

    Posted by Sheena Hicks on February 1,2010 | 07:46 PM

    I read the story and I am not in awe or amazed. Black americans have been contributing to America and all aspects of this for generations. The sad part is black americans have not been given the correct credit or respect.I don't think the monetary compensation would have been a big issue if the proper respect and acknowledgement had been given at first, which most self-respecting people ask for. It is so sad that our country, a country who many people from other countries come to for 'the promise' has such a disrespect for the so called second class citizens-Black Americans- who made the ultimate sacrifice to the country we love.

    Posted by Jan on February 1,2010 | 07:46 PM

    Simply fascinating. Your research is commendable. Your hair must have been standing on end the entire time you worked on this book. Best wishes for your future efforts.

    Posted by Bethany Hoyle on February 1,2010 | 07:46 PM

    This is an amazing story

    Posted by Mheka on February 1,2010 | 07:47 PM

    I think that is a wonderful story that is true. But the out come of this is for us is that when we hear tell of children that want to quit school buy them that book and they will no that if we stay in school till the end we will learn something and not being at the tail in of things without a clue.

    Posted by Patricia Dawkins on February 1,2010 | 07:47 PM

    But that is still exceptional that the cells have reproduced and lived forever because most peoples cells have written into their cell gene code a specific time when the cell will die. a sort of programmed cell death if you will.

    Posted by dallas lehman on February 1,2010 | 07:47 PM

    It was really a great story...but before we judge.. I think we should consider looking on both sides, I mean, the part of the family and the scientist.. so, where can I find this book?

    Posted by april rose on February 1,2010 | 07:47 PM

    Wow.Great story.

    Posted by on February 1,2010 | 07:48 PM

    This story is so intriguing and captivating. There are so many lessons to be learned in this short narrative of the HeLa cells. I want to know more and I will share this remarkable piece of history with my family and friends. Thank God for Henrietta Lacks, the doctors who took the samples (be it right or wrong) and for you, Rebecca Skloot, for your dedication and determination to bring her story to light.

    Posted by Sharon Cooley Johnson on February 1,2010 | 07:48 PM

    The scientist did not get her consent. What proof do we have that he was not a malicious racist scientist? TRhe other scientist involved was not originally honest about her name to intentionally promote a cover-up
    He did not get the cells from a white woman. What would the protocol have been for a married white woman? How so many years after the fact can the writer speak for what was in the heart and mind of that scientist/doctor? So many black women even in 1951 were butchered as a form of sterilization

    Posted by Patricia Williams on February 1,2010 | 07:49 PM

    very fascinating story. sadly she was never told and knew that she would end up helping cure people indirectly.

    Posted by mikeca2da on February 1,2010 | 07:49 PM

    The title is misleading for the simple minded people. It is not that this womans cells are truly immortal and will live forever, what it truly means is that there are still cells from this woman being used in science because they were duplicated and grown so many times and for so many years that , in essence, part of her is still alive and will continue to be, but its only cell cultures, its not a human being that will live forever or something along those lines. It is not like SHE is "living forever" or something, but by making it SOUND like that, it DOES make it more interesting and grabs peoples attention none the less...

    Posted by jjjbbb on February 1,2010 | 07:49 PM

    This is very disturbing. I am appalled, but not surprised by the number of people who are ok with this.

    THIS IS WHY NOONE SHOULD DONATE ORGANS. The hospitals benefit monetarily. The doctors benefit monetarily. The patient gets the organ. Everybody benefits except the donor and the donor's family.

    Posted by brainsmasher on February 1,2010 | 07:49 PM

    This was really interesting. I liked it alot.

    Posted by kristina on February 1,2010 | 07:49 PM

    Interesting from a human point of view. I am guessing some law firm is cranking out a lawsuit on behalf of the family. The problem is, we as individuals are not in a position to profit from our cells, unless we happen to own a research lab and have the money to develop some new and useful products from them. That takes millions of dollars. Yes, pharmaceutical companies have profited from Helen Lacks' cells, but they also risked the capital to develop them and the derivative products. No resultant vaccines, etc., no profit, only loss--- would the Lacks family also participate in that? Interestingly, there is another well-known cell line, known as WISH cells, named for Westminster Institute (the research lab which cultured them originally) and Sarah Henderson, who provided them.

    Posted by john meaney on February 1,2010 | 07:49 PM

    I LOVE THIS STORY. PLEASE GIVE ME THE NAME OF THE BOOK AND WHERE I CAN PURCHASE IT AT.I ALSO WOULD LIKE TO KNOW THE AUTHOR TOO

    Posted by t. wilson on February 1,2010 | 07:50 PM

    This is truly an amazing story! If children today were just as inquisitive as this young lady. Way to go and find the truth.

    Posted by leonore on February 1,2010 | 07:50 PM

    This story was just the beginning. It's a certainty that some people today carry genes that would benefit others. One being rapid injury recoverly after sustaining an injury.Self healing seems to never been a subject of medical research.

    Posted by Obed Elland on February 1,2010 | 07:50 PM

    Fascinating!

    It reads like a great fiction story, but to think that this is truth is amazing.

    It will no doubt be one of the greatest pieces of journalism in a book, very similar to "Roots".

    Great job!

    Posted by Fernando Lundy on February 1,2010 | 07:50 PM

    I love the photo shivers me back to the moment of, you know

    Posted by on February 1,2010 | 07:50 PM

    You know, it never ceases to amaze me regarding hidden agenda of our American people. Once again, the use of non-exposed experiments, in the name of science, are used in being used in the name of science.

    This is not the first instance where an entity experimented on individuals without their knowledge (family included).

    LSD Experimentation was another such incident. I understand that this is interesting and I want to read more. After all this time, what are some of the conclusions that have been reached at the expense of Ms. Lacks' sacrifice in the name of science. This is very, very interesting. I have many, many questions.

    Posted by Karen on February 1,2010 | 07:51 PM

    Ok,but as artist-somebody needs to photoshop that old picture.

    Posted by Joe Thompson on February 1,2010 | 07:51 PM

    I find this story fascinating!!! To the people stating that the family doesn't deserve anything is crazy to me. Remember what happened to the Tuskegee Men. Lies have always been told about Afrian-Americans and our contributions.

    Posted by REIGNBOW on February 1,2010 | 07:51 PM

    This is really interesting. This should be taught in all schools.

    Posted by Danya on February 1,2010 | 07:51 PM

    This was a very good story. Very interesting!

    Posted by Carole DeLaney on February 1,2010 | 07:51 PM

    I agree with whats been said but this is what happens when you are treated as ignorant, this same thing can hap pen today with our youth. Let's be honest with ourselves if education is the key for this not happening again then, look at our current situation our kids and parents signing papers not knowing what they are giving up. This is 2010 and I pray that all participants that wrote comments share this story with as many people you know because you could be helping someone to not be another Henretta Lacks without there permission and due compensation if they want it.

    Posted by PWM-SOJ on February 1,2010 | 07:51 PM

    The story is fascinating.It is great for Henrietta Lacks and she is lucky that her cell is a great contribution to science,medicine and humanity.This world is not perfect.It is absurd and ugly that Henrietta's consent was not asked.Had she consented to this,the story had been perfect and we know that this did not happen.It is a must that her children/kin be taken care of their needs anyway the result of taking her cells is worth,what billions?

    Posted by yolanda pacudan-yarcia on February 1,2010 | 07:52 PM

    I love the photo it takes me back where i did not exist, and I wish I knew the mystery of being here right now

    Posted by Al on February 1,2010 | 07:52 PM

    a very good story and a clueless heroine who did not know she contributed so much in modern medicine in helping save mankind. but what destroyed this beautiful story is TREACHERY & GREED. scientists and those big medical corporations stole parts of her and profited bigtime in this multi billion industry, while henrietta's family wallow in poverty and ignorance. what a shame!

    Posted by zdrx on February 1,2010 | 07:52 PM

    If you "owned" your cells then forensic teams that collect cells for DNA analysis in criminal cases could not collect them off items either. Like a suspect spits out his gum and the forensic people would have to say, excuse me sir do you mind if i swab your dicarded gum to be used in a case against you. You can't bend rules for certain people.
    Also, the daughter learned nothing about her mother that her dad couldn't tell her. And the racial/socioeconomic cards dont entitle her to anything. But the Books author would be nice to give her some proceeds as a gesture.

    Posted by Kyle on February 1,2010 | 07:53 PM

    Bottom line...the cells were taken WITHOUT her knowledge or permission. The intent of the physician were not honorable to the patient. He had alterior motives, unbeknownst to her. THAT WAS WRONG. Money was made... millions... and the family of this woman need to be compensated. Regardless of her ethnic origin, it was a breach of trust and confidentiality.

    Thank you Lacks family for your contribution to saving millions of lives. You are due restitution and acknowledgement.

    Posted by Green on February 1,2010 | 07:53 PM

    That's a nice story, but you need a little more scientific explanation as to why her cells were immortal. More biological details!

    Posted by alec on February 1,2010 | 07:53 PM

    I believe this is a great story, but let's be honest there are hundreds of thousands of people making money off these cells and the family should reap some of the benefits. We always want to say, "oh how this is such a great thing for man kind," but they didn't get her permission and they should compensate the family. I would bUy the book, but some people ought to stop making excuses. . .How quickly we forgot the "Tuskeegee Experiment". . .I guess you think that was also done to benefit mankind. It's just ironic that the survival rate for African-Americans who die from cancer is so low as compared to European Americans. . .We shouldn't make excuses, we should be fair and that's the TRUTH. . We talk about the fact that we don't seek help until it's too late. We'll if I can't afford Healthcare is that really my faught. . .I work everyday and I have two (2) degree's but I can't always afford healthcare. We need prevention and that means healthcare for all mankind. Nor just the one's who can afford it. .ZAN

    Posted by Zandalisa H on February 1,2010 | 07:53 PM

    Are cells able to grow forever. then you would think it would be easy to find the cure to cancer. they do stem cell transplants all the time,

    Posted by T on February 1,2010 | 07:54 PM

    Why do so many people instantly reduce everything to "How much money can I get." It shows who much greed prevails and how little character the person has. The scientist or doctor who did this is probably already dead, and who knew that these cells would multiply and live on and on. No, it should not have been done without her consent. However, that was before the days of everyone suing everybody else at the drop of a hat. All the good things that came to life by the research on Henrietta's cells have helped millions of people. Her children have probably had the polio vaccine. Someday the research enabled by the HeLa cells may even save the life of her children or grandchildren! Cells are shed by the body every minute of life, some dead and some alive. That's how a lot of DNA is obtained. You lick a stamp, you leave some cells. Do you demand payment? Of course not. What has happened to the milk of human kindness that someone would demand payment for something that could save the life of another human being?

    Posted by Fran on February 1,2010 | 07:54 PM

    This a great story !!! I can't recall where I once heard a prophecy spoken, that the "Cure" to Cancer would be something so simple that the answer would be right in front us.

    Posted by Tony Guerrero on February 1,2010 | 07:54 PM

    I am really sadenned to read about Henrietta Lacks and family The scientist were collecting these cells at a time where black people were not given any rights as citizens of this country. The family has been taken advantage of. The time this occurred, poor black farmers, was at a time she nor the family had the rights of caucasion citizens. ie The Tuskegee experiment. It makes you wonder were they even trying to treat her cervical cancer or deceiving just to obtain the cells to be used for further clinical studies. Everyone made money from the use of her cells. The scientist, pharmacuetical industry, even the author of the book The Immortal Life of Henrietta Lacks. It is a shame that this family received nothing from her contribution made. They should not be homeless, should have health insurance and guarenteed an education.

    Pat

    Posted by Pat on February 1,2010 | 07:54 PM

    So the author criticizes Mrs. Lacks son's for seeking monetary compensation yet she charges money for this "book". If money and fame was not the driving force behind this whole theft and conspiracy why is this book not being freely donated to schools and libraries? Nothing done in the name of science and research is solely to help mankind money and fame is always first.

    Posted by notimpressed on February 1,2010 | 07:54 PM

    i cannot imagine that being my mom's cells being used in this manner without anybody's consent and permission. That's ridiculous.

    Posted by Rene T. on February 1,2010 | 07:54 PM

    The cells are "immortal" because they are cancer cells. Most ordinary cells have a number of times they can replicate, with the telomeres at the ends of the DNA shortening each time the cells replicate until they are so short that the DNA can not / will not allow the cell to replicate. Cancer cells can completely replicate the telomere ends and can replicate indefinetly. - Read - Elizabeth Blackburn and the story of telomeres - deciphering the ends of DNA
    by Brady, Catherine. MIT Press 2007.

    Posted by Gerard Mittelstaedt on February 1,2010 | 07:55 PM

    intersting.... Now is the HeLa cells the only "immortal" cells or are there others?

    Posted by Taylor B. on February 1,2010 | 07:55 PM

    (They went up in the first space missions to see what would happen to cells in zero gravity.)Henrietta, was the first human in space then ?.....amazing. the cells were alive.

    Posted by gerry on February 1,2010 | 07:55 PM

    this is a phenomenal event in the history of science and medicine...i think there should be an agency in the field of science and medicine to recognize the Lacks family, or even compensate them accordingly.

    Posted by Reagan on February 1,2010 | 07:56 PM

    This story intrigued me even though I never did very good in science, period. The way it is explained, just in the short story version, is pretty basic, so that someone like me can understand as well. I do agree that people who allow their tiisues, etc., should be minimally compensated. But in the full retrospect, everyone needs to think about the good that can come from simply GIVING a peice of one-self, for the good of others. I going to be looking for the book!

    Posted by tasha crutcher on February 1,2010 | 07:56 PM

    Behind every scientific fortune... There's a crime.

    Posted by TheBigMansini on February 1,2010 | 07:56 PM

    Wonderfull story I can understand the questions about family recieving something from any money made from what was learned from the cells. However I look back to the 50's and remember all I went thru with heart surgery and told I would die because they could not do anything for me,then they perfected the heart and lung machine so long heart surgery could be done. My operation was done the year the Dr's thought I would die and because of what they learned from my surgery and others like it at that time there have been a lot of very young lives saved. We were never rich and I have had to work for everything in life that makes me and family happy. I am happy because every time I hear that a life has been saved because of what was learned with my experience with medicine I am very proud and happy that I have contributed so much in this lifetime.This is one of the best written articals I have read in a long time very informative and inlightning to people who don't think on these things often.

    Posted by Nancy Clayton on February 1,2010 | 07:56 PM

    Awesome!! I was doing a small research on immortalized cell lines, and discovering that the start of human cell cultures came from this Henreitta Lacks. She's a woman, and she's black, and she changed the world of biology!

    Coolest thing is, she's "continues" to live on...!!! haha, neat. ^_^

    Posted by The Lone Moon on February 1,2010 | 07:57 PM

    pretty cool stuff! hah

    Posted by annnna on February 1,2010 | 07:57 PM

    This is a fasinating story. A great way to kick off black history month! I think I will have to get the book. Thanks

    Posted by Jessi on February 1,2010 | 07:57 PM

    This Is Proof That Nubian Blood Is "THE GENESIS OF LIFE"

    Posted by jimmy on February 1,2010 | 07:57 PM

    The cells continue to live because they are cancer cells. If we can find out what will kill them, maybe we can kill cancer, too. Her family has every right to launch a lawsuit. They are her heirs. Her cells were taken without her consent and others have made money from them. If it wasn't for her, those experiments never would have been successful. It is also interesting to note that she was a tobacco worker. Tobacco is supposed to cause cancer, besides everything else we eat, drink, smoke or imbibe in. Yet her cells seem to be important in research due to her exposure to tobacco? From what I get out of this is that you get cancer from tobacco use but tobacco use has also saved many lives through research. Her family deserves some money!

    Posted by lee on February 1,2010 | 07:57 PM

    Captivating story! Thank you for all your efforts!!

    Posted by Chris on February 1,2010 | 07:57 PM

    The closest thing I've heard of that could be the holy grail. I've heard the holy grail could actually be a blood line.

    Posted by lisa on February 1,2010 | 07:58 PM

    This was a very interesting story. In the 1950’s all kinds of unethical medical experimentation went on in the U.S. and other countries. Many of these tests and experiments were preformed on uneducated, disabled people or also known as the indigent simple minded. This was accepted practice back then; However, as then and today many still feel it was highly unethical. As to the current story, it needs to be read and shared. I too think it would make a great movie. The family should get some compensation from the book and eventually movie. Because this would make a great human interest film

    Posted by Diana on February 1,2010 | 07:58 PM

    WOW how weird! maybe shes a unique human

    Posted by Jessica tii death on February 1,2010 | 07:58 PM

    Great article. I'm looking forward to reading the book.

    Posted by Tammy on February 1,2010 | 07:58 PM

    "Henrietta-Lacks Immortal-Cells" is a fascinating story. I am so interested now in readind the book. I pray her family is WELL compensated. I read some of her decendents are homeless and poverty stricken. Henrietta, herself was considered a poor tobacco farmer. I think Henrietta paid a great service to Medical Research. The 1950's proved to be very harsh, prejuiced, period. Even for healthy, poor Black woman survival was not easy. I can't begin to imagine the anguish she endured, Was there a hospital or doctor that would treat her a poor Black woman? Would she and her husband turn to their faith her ncuriable illness, had she ever seen a doctor before? Did she cry silent tears or suffer wondering why was she stricken with cancer? I believe God had his hand in this from the very beginning!

    Posted by zanee on February 1,2010 | 07:58 PM

    1950's come on, the black people were taken advantage of in that era, so we know why the family wasn't compensated.How many vaccines was made with this young mother's cells. They treated her and her family like she was a LAB RAT!

    Posted by Barbara Hilliard on February 1,2010 | 07:58 PM

    OMG That is so crazy they could of help out the family they used the mom in some way so really she help out a lot in a good way for folks and then in a bad way for using her as a clone I think they own the daughter and son every red penny NOW AND FOR EVER AND UNTIL IT PASS ON FOR THEIR KIDS SO THEN EVERY OTHER RACE HAS BLACK IN THEIR BLOOD WOWWWW THAT IS WHY A LOT OF STUFF THAT HAPPEN BACK THEN WAS HUSH HUSH NOW IT MAKES YOU WONDER IF THESES OTHER VIRUSES...WHERE MAN MADE AND USED ON OTHER PEOPLE TO SEE HOW THEY WORK MAN IS WICKED WOW LET US THINK NOW

    Posted by JESTIC on February 1,2010 | 07:59 PM

    Nicely done. Excellent conclusion. This is an article that should be shared.

    Posted by Geaux Jeaux on February 1,2010 | 07:59 PM

    Glad to have read this article, but her Mrs. Lack's family should receive restitution. A film should be made about it too and the family get some of the proceeds.

    Posted by Joz on February 1,2010 | 07:59 PM

    i love your article

    Posted by angelica on February 1,2010 | 07:59 PM

    This is very interesting and amazing.

    Posted by charly Zeph on February 1,2010 | 07:59 PM

    What a great piece of black history...I will put this on my list to read.

    Posted by Crystal on February 1,2010 | 07:59 PM

    This is extremely interesting. I wish there was some way to get this out to the masses. I am a guidance counselor at a high school in Chicago. Guess who I am going to see first thing in the morning at my school? The biology teacher. At least my students will know about this.

    Posted by Donna on February 1,2010 | 08:00 PM

    To all of you who made negative comments about Henrietta, and the writer, it is obvious that you do not have any kind of education whatsoever. Showing just how ignorant you are is ignorant. This was a very interesting story, very educational. To the person who took the time out to research this information further, my hat goes off to you!

    Posted by Tremeka M on February 1,2010 | 08:00 PM

    This story demonstrates the interdependency of the human specie. It is unfortunate that we sometimes tend to over look this in our dealing with each other. I also hope that the family will eventually get something out of all this.

    Posted by Mike Reid on February 1,2010 | 08:00 PM

    what an interesting piece of history!

    Posted by susan on February 1,2010 | 08:00 PM

    What a great STORY! Amasing! I will send it to my son's email address he need to read this wonderful article. But i hate to those people who stole her cells because it is against the law of the people and the law of our Divine Creator. Further, the family should recieve what is just for them. Living in misery some members of the family she left while the other enjoying fame by stealing.
    Anyway, could please send me a details where i can buy a copy of your book. God Bless to you. Nelson Desipeda fron the Philippines.

    Posted by NELSON G. DESIPEDA-PHILIPPINES on February 1,2010 | 08:01 PM

    Amazing! whao very, interesting.Keep up good job.What can i say.

    Posted by Jaycee on February 1,2010 | 08:01 PM

    Brilliantly done. :) I should remember to look this up.

    Posted by Zachary Zoet on February 1,2010 | 08:01 PM

    That's still amazing, anyone with a basic knowledge of biology knows that cells eventually die. I would very much like to know how they explain it.

    Posted by Victoria on February 1,2010 | 08:01 PM

    Of course it will turn into a racial issue, it's the poor black lady getting taking advantage of by the rich white man. Now the poor black homeless man who wouldn't find a job sure knows how to find a LAWYER!! Yawn

    Posted by Jim on February 1,2010 | 08:01 PM

    This is an interesting story. The author mentioned in the article above that "scientist don't know why Henrietta Lacks'
    cells keeps living and multiplying" Let us focus on asking the questions why the cells keep living instead of the race aspect of the article(maybe also in the book), that the Author injected to raise a greater attention to her book.
    We should be asking scientists whether or not this phenomenon is significant to researches that can improve the quality of Lives.

    Posted by Stephen Elsar on February 1,2010 | 08:02 PM

    A wonderful story. It was a timely one due to Black History Month!

    Posted by Charlina on February 1,2010 | 08:02 PM

    Why can't people just accept that thats the way it happened. If you think the family deserves restitutions then I, a white male, think I deserve them too, after all somewhere way back when I had an ancestor who was a serf in England and they had a ancestors who were straight up slaves just like Africans in early America!!! GET OVER IT, and just accept that the world isn't perfect and complaining and whinning only makes it worse. GREAT ARTICLE, can't wait to read the book.

    Posted by on February 1,2010 | 08:02 PM

    Amazing!Is that book available already in Philippines? ..interesting.

    Posted by Maria sabel on February 1,2010 | 08:03 PM

    nice article, wonder how many cell cultures were contaminated by HeLa. Can hela cells really fly to contaminate other plates? If true, it is terrible! Have to go check my cell cultures in the lab.

    Posted by ninuo on February 1,2010 | 08:03 PM

    Yes, this story is very interesting and apparently thru the years have helped many, many people to have good lives and cured of so many different things. I also believe there should be some compensation to the family of this lady since they apparently needed it and would be more reeptive to scientists now to carry on with more history and possibly donating their own cells.

    Posted by Grace Stark on February 1,2010 | 08:03 PM

    This is so compelling! This is a story that should be in our hisory books - amazing. Great story!

    Henrietta's family should be compensated

    Posted by Liz on February 1,2010 | 08:03 PM

    Very interesting story - will a percentage of the proceeds from book sales go to Mrs. Lacks' descendents? I'm fascinated to know how the cervical cancer cells did not replicate as cancer in the case of the research for the polio vaccine.

    Posted by naj on February 1,2010 | 08:03 PM

    Interesting...

    Posted by anon. on February 1,2010 | 08:04 PM

    make sure the young kids get the knowledge.

    Posted by ronjustpaint on February 1,2010 | 08:04 PM

    I the hook is to read the book to find out about the compensation to the family. depending on when they sued, I would not be surporised if it is still in ligigation.

    Posted by Eva on February 1,2010 | 08:05 PM

    I don't think that HaLa is the only one. My mother used to tell us a wild story about her mother died early 1952 of cancer. She said that they kept the cancer alive by feeding it and on my grand mother's death they offered money for her body for expertments. The family hid the body until it was to decayed for medical use before they burried her. We just thought this was some wild story that she made up until this book was published.

    Posted by Diana Elsey on February 1,2010 | 08:05 PM

    These cancerous cells have been used to prepare vaccines. Viruses are known to play with the DNA of host cells in order to replicate themselves.
    Aren't cancer cases on the rise ?.

    Posted by Carlos on February 1,2010 | 08:05 PM

    The great British documentarian Adam Curtis made a remarkable film about this in 1997 titled "The Way of All Flesh." It's nice that a book has come out to expand what he uncovered.

    Posted by Nat Segaloff on February 1,2010 | 08:05 PM

    I read an article in the Feb. O Magazine about Henrietta Lacks. I will definately read the book. She had a rough life, like so many poor women.

    Posted by geegirl on February 1,2010 | 08:06 PM

    For me, this is just another example of how black people have been mistreated by the white system in this country. It was stated that Henrietta Lacks' cells were taken without her knowledge and used for very successful studies and to benefit the WORLD and yet for most of their lives Henrietta's family has lived in poverty. How on God's earth is this correct? And now that's it's known why hasn't this been rectified??? When this country interned the Japanese back in the 1940's, the U.S. government later saw fit to pay reparations to them for lost property, etc. but this woman's very essence is taken without a backwards thought??? As was stated, BILLIONS of dollars have been made through the years off of her cells that have multiplied and not died out completely. And they haven't received one red nickel.

    Were there reparations for those of the Tuskegee experiment?? This PROVES to me that no matter what has been done to those of OUR race we will NEVER have the justice due to us from this country. We, as a people, have continually been "enslaved" in this country and it will never change. So much has been done to us and it continues...

    Posted by D. Scott on February 1,2010 | 08:06 PM

    Wow great reading----And what a nice looking couple.
    To awesome Thank You

    Posted by cindy on February 1,2010 | 08:06 PM

    It's not shocking or amazing that the contributions of blacks in America have been omitted from American history for centuries because of racialism. When will America live up to it's creed to set the record straight ?

    Posted by Danny Kaye on February 1,2010 | 08:06 PM

    Facinating. But Black people are not the evil targets of medical research. Rather medical research and training is commonly done with poor people whether Black, White, or something else. Teaching hospitals are usually research hospital and research hospitals are usually teaching hospitals. Henrietta needed care and she was poor. So she received care at this hospital and that made her cells available for research. Teaching and research hospitals need human subjects. So it is a trade-off. And if poor people are accidentally killed the liability to the facility is much less than if a rich person was killed. Research does not always work out as hoped. That is true whether that rich person is White, Black, or some other hue.

    Posted by Tim Tyler, Ph.D., Attorney at Law on February 1,2010 | 08:06 PM

    If this true... any human tumor cells that human being can live forever by means of cloning in a differnt person.Like the Scientist did in the story. All God creations cannot die in Earth? Bu How it will Be? many questions asked and its very complicated or maybe there is Life after death.

    Posted by Rowena Ramirez Vizconde on February 1,2010 | 08:06 PM

    That picture of the couple eerily looks like Papa Justify and Mama Cecile from the movie Skeleton Key. Just saying. Nothing malicious. :)

    Posted by SelfPotato on February 1,2010 | 08:07 PM

    this is a good start in the process of honoring henrietta lacks and her family for her contribution to mankind, heroic.

    Posted by jenito m asequia on February 1,2010 | 08:07 PM

    Interestingg!! How can I give a sample of my tissue cells.? My family has a history with Alzheimers Disease. How can i find out if its genetic? Also, is there anything one can do to possibly prevent it!.??

    Posted by Luis Rivera on February 1,2010 | 08:07 PM

    great article most interesting will read the book

    from Wikipedia: " This issue and Mrs. Lacks' situation was brought up in the Supreme Court of California case of Moore v. Regents of the University of California. The court ruled that a person's discarded tissue and cells are not their property and can be commercialized. "

    check out: Further reading,External links http://en.wikipedia.org/wiki/HeLa#George_Otto_Gey_and_Henrietta_Lacks

    Posted by wyold_1 on February 1,2010 | 08:08 PM

    God's creations are everlasting. The Contributions Henrietta made to modern medicine as we know it today has saved hundreds of thousands of lives which is a testament to thw will of God and his bountiful blessings. Thanks Henrietta.

    Posted by Thomas C. Tolliver, Jr. on February 1,2010 | 08:08 PM

    very very facinating discovery!

    Posted by Dr. Ananta Dutta Shrestha on February 1,2010 | 08:08 PM

    We all are valued! Thanks to Lady Henrietta Lacks for sharing her cells with us ( even without being informed or giving consent to doctors). Talking about finance, will the daughter or the family be compensated from the book sales? or will they be given credit for their contributions to author. When people are exposed in their wrong doing, how quick they are to point out someone lack of knowledge. That why we appreciate and acknowledge God, King of kings, and the Great I AM.

    Posted by Mary Archille Crank on February 1,2010 | 08:09 PM

    An excellent piece to read. The book is something I would like to read. Written with intelligence, thoughtfullness and respect for the family. Excellent

    Posted by hilary on February 1,2010 | 08:09 PM

    no the family cannot sue because every cell in your body every peice that makes you is owned by another company if a person were to have the cure for aids in there blood their doctor can patent that sample and then owns it not of course while it is in the body but if it is ever removed it cannot be sold or used for anything

    Posted by marshall on February 1,2010 | 08:09 PM

    It's great that this is getting attention in the mainstream, however, it's completely disingenuous to imply that it is any sort of secret. Henrietta Lack's name, ethnicity, and story are well known throughout the biomedical science community.

    Additionally, there's nothing remotely mysterious about the immortality of the cells: they're cancer cells which therefor lack growth inhibition. I strongly oppose the dishonesty of the writer of this piece. It's not just pathetic, it's an affront to the subject and the individuals involved.

    That said, people should be aware of this story, and, just to bend your mind a little, consider the fact that Henrietta Lacks died in her early thirties, yet can quite possibly claim to have the most living cells of any human being, as well as being on course to become the oldest at some point this century.

    Posted by Connor on February 1,2010 | 08:09 PM

    I hope her family was eventually compensated for her invaluable contribution to medical research and science in general. This is definitely my next book to read! I remember something about HeLa cells from A & P but I wish I would've gotten more out of the lesson now. So fascinating to think of all the people she has helped!

    Posted by Jana on February 1,2010 | 08:09 PM

    "Can the family of H. Lacks file a lawsuit against the scientist?"

    Yea really! They should get SO MUCH out of what was discovered because of her cells.

    Posted by Camille on February 1,2010 | 08:09 PM

    RIP Henrietta Lacks. God Bless the Lacks family.

    Posted by Dawn on February 1,2010 | 08:09 PM

    Very interesting story to be shared.

    Posted by Nor Hasyimah Haron on February 1,2010 | 08:09 PM

    this is really interesting thing....

    Posted by Eden Benig on February 1,2010 | 08:10 PM

    The story is amazing. Its not only life after death but another life was perhaps saved. Or perhaps a lot of lives were saved. But the doctors should have told the relatives of Henrietta about the cells used for medical studies.

    Posted by Laura on February 1,2010 | 08:10 PM

    Amazing, Nice research... Scientists?!?.-(

    Posted by Paul Libag on February 1,2010 | 08:10 PM

    I am not sure how removal and testing of cancerous cells equates to compensation. Would you leave the cancerous tumor inside someone, or give a cancerous tumor to the patient until they decided to sell it? The fact that the abnormal cells rapidly divide and grew in the culture at that time did not mean mistreatment. In fact, tumors and other tissue is required to be examined by Pathologists to ensure that the tissue is what it is thought to be and hopefully determine that all abnormal cells had been removed. It seems that everytime something good is found someone feels entitled to compensation. Or, everytime something bad happens someone is to blame and the unfortunate person or their family must be compensated. This lady's misfortune was tragic, but the fact that her abnormal tumor grew immortal cells was a finding of science probably by chance. It is a fantastic story and I am sure it will be a great book. Give the family proceeds from the book, but I don't the scientists should be considered theives for trying to find a cure.

    Posted by Gene on February 1,2010 | 08:10 PM

    How does anyone know that she did not give permission to use her cells for study. She pobably received free medical treatment in return as they tried to cure her. I have donated blood and platelets and have never received any money. I do not know who received blood from me or how it was used.

    A lot of time and money has been involved trying to find cures and causes over the years. If science had not used this lady's cells they would have probably used cells from another cancer patient.

    Searching for cures is very expensive and many, many people are involved. One person would not get rich from research from someone's cells.

    Posted by sjm on February 1,2010 | 08:10 PM

    that story was amazing,it's crazy that the family was looking to make money off their mother who i'm sure would have giving her cells for free if she knew it help other people.My daughter who is sixteen read this and she was as amazed as i was and now will be looking more in to learning about this wonderful women.

    Posted by atiya harpe on February 1,2010 | 08:10 PM

    WOW, such a wonderful story!!! Great information with the hope that through research, so much more could happen!!!

    Posted by Jean on February 1,2010 | 08:10 PM

    thank you for this info..

    Posted by smitty on February 1,2010 | 08:10 PM

    As a poor farmer, most probably the tax dollar paid for her treatment. So she was paid-off by Goverment, this means by every american. IRS collects day to day from benefits obtained from the HeLa cells. Family should profit from the book. Hundreds, may be thousand of cientist who made life easier, never profited from their work for humanity and many died in poverty. The Edg 1 affair is frightening, but as after 59 years we don´t have seen the HeLa Disease, we should not worry about; yet. Can cancer be spread through dust particles?

    Posted by Rudy on February 1,2010 | 08:11 PM

    i love this story. i find it amazing in every way. i'm a 35 year old punk rocker, and i found myself welling up in tears because of this article. not so much the article, which was well-written, but what the story says about the lives we all lead. one of the first comments on this article was someone who said "everything that lives, dies..." i am one of those rare few who believe otherwise...have seen and felt otherwise. nothing that is will ever truly "end." life and death are perspective artifacts.

    Posted by shawn on February 1,2010 | 08:11 PM

    After reading so many comments on this article, i would like to 1st say that the family should indeed get some compensation from the hospital and the author. Back in then racism was at its "power" years, meaning that minority basically didn't have proper means to defend or prevent this from happening. The cells were"stolen" from her without her consent or knowledge. Please remember that although her cells are "grounbreaking" in its usage, we would be either too naive or ignorant to feel that money is not involved.

    Money was made through this, and whether we like to admit it or not,MONEY is the end product of all of this. Whatever goes for the betterment of mankind, money is involved some way or the other. This book for instance, while its information is a good source for future research and information, its author will get some compensation on its sales. Someone quoted:
    " If I blew my nose and threw it in the trash and somebody found it and used it to do research, I wouldn't expect to make money off of it.
    Posted by Tim on February 1,2010 | 12:52PM."

    This really shows "IGNORANCE". This person doesn't realize that the cell was "taken" from her body without her knowledge or consent. It NOT the same as you throw it in the "trash". I guess i could go further and say the the word"trash" is aimed at the "poor black" woman. This book will make some money and the hospital has already made and will continue to make money on this. The natural thing to do is apologize , compensate, and thank the family for the contributions made from the cells of Ms.Lack. Also, the family may have the same cells in their bodies, and if they agree to be tested to find more cells like Ms.Lack and help with the betterment of mankind.

    Posted by Dayne in Japan on February 1,2010 | 08:11 PM

    I totally agree with what everybody is saying. This Family should put a lawsute aganist the sicentist and they should get half of the profit that their making. They have been using this womans cells to create vaccines to save peoples lives. I think that is just shady and greedy how you can keep something like that from the decendents of this woman and keep it a seceret. I think this is totally unfair and they took advantage of her and the situation. I am extreamly proud that this African-American woman was able to have her cells used to create vaccines, and now the family sould be compensated for it.

    Posted by ashez on February 1,2010 | 08:11 PM

    This was definetly a good and interesting story, and to top it off it's a true story. Wow...if anything, she's become famous after death. I will definetly buy the book.

    Posted by on February 1,2010 | 08:11 PM

    What ?? Jungle bunny Genes were used ???? They aren't even Human , for Christ's sake .... Well, I guess it's like using lab rats , or Monkeys .. Same Difference ...

    Posted by Dale on February 1,2010 | 08:11 PM

    wow alot of info I didnt know Its cool to heare all the things her cells have done and for all you racist fools out there heres a black woman cells that are helping EVERY ONE today thats just Really cool, I SO REALLY Hope the Family gets ALOT Of Money from all of this espiciall since it was taken from her with out promision and The family has all the rights to ALL the Royaltys its not rite for otheres to be making millions and millions on her and the family get nothing, I truley Hope They Get A Great Piece of it all it was there mothers cells You Go HENRIETTA A TRUE AMERICAN HERO

    Posted by larry on February 1,2010 | 08:11 PM

    God Creations cannot die. Is there really a "Life after Death"? No one knows.. Except that when time comes that I die and I'll be the one to answer my question.

    Posted by Rowena Ramirez Vizconde on February 1,2010 | 08:11 PM

    Are the cells immortal because they are cancer cells? Cancer is hard to destroy.

    Posted by Maggie on February 1,2010 | 08:12 PM

    This is a very interesting story, it should generate a lot of interest in your book. However, perhaps you should consider donating a portion of the books sales to the family. Or are you just another person who benefits from Mrs Lack's cells?

    Posted by Craig on February 1,2010 | 08:12 PM

    I have used HeLa cells in my researching past, and no, I didn't earn a penny of profit from the effort. Like most scientists, I just tried to push forward the boundaries of what we know.

    I am awed and delighted to now be able to trace the story completely to it's roots. When I worked with the cells, I was initially told the 'Helen Lane' story.

    I believe that Henrietta Lacks has made an enormous contribution to Medicine and to mankind. And I am even more delighted to see that it was a black woman who did so. While I cannot condone the manner in which the cells were obtained, I note that my concern today is aimed at a 1950's approach to science which still had much to learn about ethics and intellectual cellular property. Henrietta taught many of those lessons herself!

    The others that participated in all that HeLa cells have helped discover need also to be acknowledged as I hope the book does. For as committed and unique as the contribution of Ms. Lacks, so too was the dedication of the researchers such as Salk and Sabin, and the thousands of others who have nurtured, fed, stimulated and cajoled and interpreted information from an enormously valuable resource. Henrietta has been speaking to scientists for nearly 60 years. To put a face to the contribution is especially wonderful.

    It is uniquely American to talk of compensation. But add to that discussion what ought to be expressed clearly: the wonder and appreciation of generations of healthy, thriving and increasingly educated people who have the very basis of Hernrietta Lacks to thank: her cells.

    Posted by on February 1,2010 | 08:12 PM

    WOW What a story.The fact Her cells helped mankind is GREAT
    It is fantastic .
    But why should her family get money for it??? This happened over 50 years ago.
    Her son was homeless , which is terrible-but I assume he is an abel bodied man, let him find a job and make himself not homeless.
    Why is it always about money and looking for someone to take to Court and get money for something that had nothing to do with them personaly.
    Work for a living-don't try to take-take take!
    It does not matter what race she was, if her cells helped make the world a better place, isn't that enough?

    Posted by Dan Lesher on February 1,2010 | 08:12 PM

    You would think since her cells were taken without her permission, every for profit medicine developed with them would owe some type of royalties to her family

    Posted by Trace on February 1,2010 | 08:12 PM

    Have these magic cells been found in other people and was it only ffound in her cancer cells. maybe there could be many more ways to develop these magic cells and how they might benefit many humans. It should be only right that the family members should be able to get out of poverty through thier dead mothers cell benefits

    Posted by P Dickson on February 1,2010 | 08:13 PM

    This is the most interesting piece of history/news that I have read about in a while. It is so amazing how one person regardless of race, color or ethnicity can change someone elses life. Kudos to Skloot and Zielinski!!

    Posted by Kiwi on February 1,2010 | 08:13 PM

    wasnt that the picture from the movie the skeleton key ????

    Posted by jeff goward on February 1,2010 | 08:13 PM

    Why is it that race comes into every conversation or that when someone does something good or bad from a decades ago that their descendents should be profited or punished by that? I saved many lives, black and white. I never considered going back years later to their descendents to expect some reward. Some facets of our nation now expect to be paid for anything good that their foreparents did but do they expect to be punished for anything bad that those foreparents did? Do they consider repaying anything those earlier family members received? Obviously not, just pay us for doing nothing and forget what we have received.

    Posted by Dr. T on February 1,2010 | 08:13 PM

    Why in the world is everyone so interested about the stupid money? If medical scientists compensated everybody whose tissue offered some sort of medical knowledge, there would be no money left for the actual research!!!!! Anybody that has a biopsy that turns out to be precancerous or cancer has their tissue researched and discussed. All the advancements made in breast cancer, for example, were made by studying several different tissue samples. Should they all have been compensated??

    Posted by Jessica on February 1,2010 | 08:13 PM

    Mingee\\This is an amazing story. I learned about HeLa cells in biology as we all did but were never told of the origen of those cells. Excellent!!!

    Posted by robert means on February 1,2010 | 08:13 PM

    I absolutely loved this article. I am not much in to science, but definately want to read this book!

    Posted by Jimmy on February 1,2010 | 08:14 PM

    A fantastic story! Thank you for sharing to remind us of the good things that come from good people that want to help more people! I wish there were more that wanted to give!

    Posted by Debi on February 1,2010 | 08:14 PM

    No doubt the family will get over their "outrage"
    when they get some money

    Posted by tuk on February 1,2010 | 08:14 PM

    When's the last time you heard of a doctor taking a biopsy and paying the patient for their tissue? Without her consent? Are you kidding me? Does anyone know where a cervix is on the human body?

    Posted by Peter on February 1,2010 | 08:14 PM

    I applaud rebecca skloot for not giving up and for staying sensitive to Henrietta´s family. I will buy the book in solidarity to her sensitivity, perseverence and for what the story in itself adds to the possibility of us getting to a time when we all value each other as humans and learn to be more humble in how we treat each other. I hope her writting style is as engaging as this article is.

    Posted by silma quinones on February 1,2010 | 08:15 PM

    Although, the information we find out about how human cells are cultured and what we find of it, is amazing and helpful for today's world of curing diseases and finding cures for other things of that nature. It is also important to never think that we as scientist have the right to take over a persons cells without their permission are family acknowledgement for their own gain. We should never take advantage as if it's rightfully our information to know, because its not. Yes its a blessing on what we would discover but we also have to respect the persons in question.

    Posted by kj on February 1,2010 | 08:15 PM

    The moment I open my account, when I saw this, about an "immortal cell", I EASILY got intersted to read it.... Akala ko sa movie lang or sa pelikula lang may immortal cells.. pero in reaL life din pala... mayroon kasi akong favorite na movie ng aking idol na si Tony Gonzaga. She has an immortal cell in that movie, she never dies. All her friends died and came many generations but still she is alive! She got married and had a daughter... to prevent the public from knowing about her immortality, she went abroad... leaving her family and Yaya... people only knew that she was dead... but many years have gone away... she return... she found out her husband lying on a bead... old... and near death.. but she is still very young... nothing changes! how about her daughter?... older than her... What an amazing topic to talk about... an IMMORTAL CELL... ANG GANDA!!! But I believe na "Everything has an end."

    Posted by Reno P. Baliguat on February 1,2010 | 08:16 PM

    Very interesting!!

    Posted by Mimi on February 1,2010 | 08:16 PM

    There must be a connection here somewhere between HeLa cells and stem cell research. Seems like a good approach to the current controversy regarding use of fetal cells for research. Why not go forward with this instead of beating an old horse?

    Posted by MARY NIET on February 1,2010 | 08:16 PM

    I think there is none real problem the fact that "cells were migrating" through the air and "contaminating other cells".

    They weren't dangerous at some extent, as I explain you below.

    As we know of today, the fact that they were from a tumor just means that those cells didn't ever stopped from grow (multiplication), which eventually makes harm to the living body because they tend to fill everything instead of dying and being purged out of the human body. This happens when their DNA is somehow altered (especially that part that regard the regeneration or the growing old).

    Such cells are not dangerous because they don't make *other cells to do the same, they are not contagious (unless they "copulate" some other cells), they cannot change the DNA of the others, in other words.

    As per why the family of HeLa did or did not receive the money they were entitled to receive, it seems that nobody would buy the book if we were disclosed all details about that here...

    Posted by Clo on February 1,2010 | 08:16 PM

    Sincere prayer will give you the answer!

    Posted by Tim Barrs on February 1,2010 | 08:16 PM

    No, I think you"ll find that they can grow and multply forever. And they will live on indifitly. Just lik the mind and, the sole. It may laydown, while the person dies, but they get back up , and live on!

    Posted by Karen on February 1,2010 | 08:16 PM

    Over the years a lot of thing did happened under the banner of science and medicine. I was born in 1942 when segregation was the law of the land in the south. The hospital where I was born was a tiny all black hospital which was seperate but not equal to the large hospital for whites. I was born premature with a birth weight of 15 ounces and the hospital did not have an incubator. I was not expected to survive. Doctors from the white hospital approached my parents reminded them that babies as small as I had not survived and asked them to donate me to science so they could study me to enable them to be better able to save other premature babies.

    My parents refused, they again were told that I would not survive. My parents took me home with their devoted care and without the support of the medical community I slowly began to thrived. ai am perfectly normal and at 69 I am still thriving. I often wonder if my parents had given me to those doctors would I have ended up being one of those babies preserved in formaldehyde.

    Posted by Bertha Rowe on February 1,2010 | 08:17 PM

    Someone took her cells without her consent, but remember, it happened in the 50s when not many people had any rights except the white people! So I think everyone should just ease off on the racial issue and emphasize on the bright side of using an immortal cell line in many breakthrough researches. I myself am a scientist and am very glad to know the source of HeLa cells after using the cell line in many experiments. We should all salute to Ms. Lacks for the amazingly immortal nature of tumor cells taken out from her. I'm sure she's thrilled to know that a small portion of her contribution has meant so much to mankind!

    Posted by Wendy Fung on February 1,2010 | 08:17 PM

    Our cell have the potential to help us immortal. The cells keep making new ones as other cells die. The reason why we aren't immortal is because this process slows down as we get older and we eventually die. It amazed me that this woman's cells continue to keep making new cells and in a way become immrotal. I wonder if the cells have slowed down the process and or if they didn't at all. Also i hope this woman's family got the money. I saw her picture and she was beautiful. Scientist need to give thanks to this woman and her family. I hope her daughter found what she was looking for too. (for the people that aer saying vampire, vampires rule!)[I am such an idiot.]

    Posted by Katz on February 1,2010 | 08:17 PM

    Everybody get over the race thing. There is only one race on this planet and that is the human race. EVERY living person traces their DNA back to Africa, the differences resulted in geographical elements over vast periods of time. We share a common soul, the body is the house we live in, not ther person we are.

    Posted by JosefineAnne Gobreville on February 1,2010 | 08:17 PM

    I like the every word in the story, It keeps me interested in every way...................

    Posted by Samuel Sumayo on February 1,2010 | 08:17 PM

    I found this story fascinating.

    Posted by Doreen on February 1,2010 | 08:18 PM

    Someone took her cells without her consent, but remember, it happened in the 50s when not many people had any rights except the white people! So I think everyone should just ease off on the racial issue and emphasize on the bright side of using an immortal cell line in many breakthrough researches. I myself am a scientist and am very glad to know the source of HeLa cells after using the cell line in many experiments. We should all salute to Ms. Lacks for the amazingly immortal nature of tumor cells taken out from her. I'm sure she's thrilled to know that a small portion of her contribution has meant so much to mankind!

    Posted by Wendy Fung on February 1,2010 | 08:18 PM

    first I congratulate Madam Rebecca Skloot for her perseverance in tracking the truth about this very interesting and important science issue of the century. Does this immortality of a cell can also lead to the immortality of man? It's fearsome.....

    Posted by orlando m. bautista on February 1,2010 | 08:18 PM

    Reminds me of the Tuskegee trial in the way they took the cells without consent. Aside from that, this article was very well written. I'm very interested to know if the family ever received compensation for what was "stolen" from their heritage.

    Posted by Ace on February 1,2010 | 08:18 PM

    A very captivating story. Should make a movie.

    Posted by PHIL on February 1,2010 | 08:18 PM

    great article i love it great i think i might buy the book !!!

    Posted by gurl u dont need to know on February 1,2010 | 08:18 PM

    Who says life is inconsequential. All the more pro-life arguments. Cells are immortal, even post-mortem. Who dare say an embryo is not a person?!

    Posted by Frances Pearl Cash on February 1,2010 | 08:18 PM

    This could possibly lead to a medical breakthrough like a cure to cancer!

    Posted by on February 1,2010 | 08:18 PM

    i was hooked to the very end. i hope to get a copy of the book...i believe they owe H. Lacks' family something for the great contribution of hela cells to science.

    Posted by belle on February 1,2010 | 08:19 PM

    Nice article. Historical events like this should always be brought out to the light.

    Posted by Gary Roberson on February 1,2010 | 08:19 PM

    thank you Sarah from Smithsonian.com. I was wondering how such an interesting article could have been found on yahoo, then i realised that they were too busy criticising the outfits from the grammy awards last night...

    Posted by on February 1,2010 | 08:19 PM

    What a wonderful article! I can't wait to read the book and get the full story.

    Posted by Gayle on February 1,2010 | 08:19 PM

    Wow...I knew nothing on the topic involving the culture of cells, and this story definitely motivates me to learn more.

    Posted by Jahlona on February 1,2010 | 08:19 PM

    Well, perhaps Einstein's family should also be compensated for scientists stealing his brain without their knowing. It seems to have been much stealing going on during that time. Just like Texco oil company stole millions from my family who owned oil fields in Gilmer, Texas and was only paid $6 per month. It's a shame how these people who have made billions on black families for nothing.

    Posted by Concerned on February 1,2010 | 08:19 PM

    Wonderful story. I would like to hear more about the science involved. Maintaining a culture this long is incredble. The original cells are long gone,this family is owed nothing. They gave nothing and have contributed nothing. They are looking for a handout. The scientists deserve a lot of credit and the story needs to be told.

    Posted by Di Albany on February 1,2010 | 08:20 PM

    This is a great article and history. I will purchase the book.

    Posted by Sherlyn on February 1,2010 | 08:20 PM

    I am amazed at the venality, ignorance and racism expressed by the majority of posters here. This was the 1950's, there was no "cure" for Cervical Cancer (and still isn't), and in order to diagnose her condition, a biopsy was taken (a procedure which is still followed today). It would only have been after the cells were cultured in a lab to check for cancer that a definitive diagnosis could have been made. It is then that it would have been noted that the cells were "immortal". There was no theft involved, and no one deprived this family of anything.

    Posted by Pavel on February 1,2010 | 08:20 PM

    Excellent! Congrats Rebecca, great story and great research. Adore you...

    Posted by Samsudin on February 1,2010 | 08:20 PM

    Awesome story. Can't wait for the movie, lol!

    Posted by hello on February 1,2010 | 08:20 PM

    This is a great article. I will be purchasing the book. You know besides her being a hero Scientists need to make sure everyone is happy with their results or ideas before they go too far. I feel sorry for the family because as well as Henrietta Lack should've been informed apart of her tissues was taken, the family should've been informed as well. They deserve more than a great reward for this matter. Its amazing that people will do whatever for money. Sure the spectacular thing about this is that she was able to save plenty of lives and big thanks to GOD for thank and thank GOD for the Scientists. Its amazing some of the stories that can help us in the future are kept a secret.

    Posted by Shamika Cherry on February 1,2010 | 08:21 PM

    I am a community epidemiologist and I specialize in HIV research. I too have known about Henrietta Lacks/ HeLa Cells for years. During my community presentations, I would show her picture and pass out her bio, so people would know about our “Righteous Contributors”. Like so many other stories, as told by Harriet Washington, ‘Medical Apartheid”, Blacks have been the victims of malevolent behaviors by scientist and researchers for so long, that the story appears normal. But the goodness of her cells, to assist in a polio vaccine, tested in space, and in vitro studies, are all contributions from this special human being. It is a travesty for her family not to benefit. In fact it is unethical to continue selling her remains without the family receiving any compensation. To right the wrong means her family should have at the very least healthcare and an education. Anything less is to continue the unethical mindset that got the name HeLa due to racial profiling..
    I will continue to sing my song even if no one is listening. I am a researcher and I sit on a IRB and a CAB so that one day I can be apart of the ‘Righteous Contributors’ to research. Feb. 3, 2010 for National Black HIV/AIDS Awareness Day (Feb. 7th), at Malcolm X College in Chicago, IL, we will have our first Bioethics Symposium: I will give deference to Henrietta Lacks in the hopes that this unethical situation never happens again!
    Community Epidemiologist, Yaa Simpson, for TACTS

    Posted by SistaYaa on February 1,2010 | 08:21 PM

    wow glad i have a will that states doctors can't take any of me for research. If I was that family I would sue for rights to her dna and 50% of all profits made for any medicine her dns founded then destroy the dna just to be sure she can rest in peace only god has right to play with persons dna.

    Posted by scott on February 1,2010 | 08:21 PM

    This article is disturbing. It brings back some disgusting memories of reading histories in charts of patients when I was a pharmacy intern. These patients did not receive treatment for various disease states that were diagnosed but left untreated and left the patient without the health care he/she deserved and requested from white doctors. Internment wasn't the worst thing that happened to some Japanese immigrants. I remember reading the history of a Japanese male imigrant who was discovered to have primary syphylis that went untreated. It was now 1971 and the man now had tertiary syphilis with the complications that go along with untreated syphyllis. Another situation: a man brought his daughter who had mongolism in to the clinic for recommendations of what he could do now to give her the best therapy now so he could hope for the best he could expect for her in the future if he started providing her with the things she needed in 1971. He was told there was nothing he could do for her and she was "doomed" to getting an "unusual amount of infections" and her life expectancy was very short. A personal note: It took the American Psychiatric Association until 1973 to declare that homosexuality was not a psychiatric illness. God knows I've seen the harm that such a delayed enlightened decision had on a number of fine young men. One of them was me. If you are looking for a public health care system, this is probably the best way to prevent such deficiencies in health care today, now or your generation may end up with far worse and more sophisticated problems in the future caused by autonomous licensed health care workers who have other goals in mind besides treating your cervical cancer.

    Posted by James Roossien on February 1,2010 | 08:21 PM

    such a very interesting piece. most people would just glance through the article but, I read through it and I think these are things that they should teach in high schools.

    Posted by maxine on February 1,2010 | 08:21 PM

    liked the article, but science is science. people donate tissues, organs, etc all the time, and they don't expect money for their donation. the family, in my opinion, is not entitled to any money from the cells. if they do...people will be lined up everywhere to get paid for their "donation". hey my mother died very young too of cancer, she had poor prognosis from the beginning and i am sure alot of tissues and samples were taken during her many operations. her cells are immortal too, because of the cancer. and if any of her cells helped others, than great...my brothers and i aren't looking for money. and hey we are poor too!!!!! so get a life people!!!!

    Posted by deb on February 1,2010 | 08:21 PM

    i do not really get this how the cells lived and so on explain it to me please and what do they mean by immortal

    Posted by Vanessa on February 1,2010 | 08:22 PM

    Another viewpoint: Henrietta, like most of us humans, looks beautiful and bi if not multi-racial. Food for thought. Maybe that's the magic in her genes....:->

    Posted by on February 1,2010 | 08:22 PM

    Ms. Skloots is to be commended for her research and article, which in recognizing and commending this unfortunate woman who unknowingly (luckily for us) contributed so much to disease control. Having said that, I find it appalling that this happened without Mrs. Lack's knowledge and that a corporation managed to accrue their mult-millions through the exploitation of Mrs. Lack's genes. Furthermore, her family, in such need, appears not to be able to access money which they are entitled to.

    Posted by Hallie on February 1,2010 | 08:22 PM

    So many of the writers here are trying to place the ethics of today against the realities of the 1950's. That doesn't work. There are so many things that were perfectly acceptable in the 1950's that are viewed with incredulous horror today. It really cannot be stated as fact that Mrs. Lack did not know of the procedures being carried out. She may have known, but not fully understood. Not understanding could easily have caused her to dismiss the implications of what was going on. I, for one, thank God for giving us this woman whose gift has helped mankind. I was in college in the early 1950's and it was a totally different world than we have today. For those who missed living during that period, I can assure you that the present and the future are far brighter than our wildest dreams in those days. I came from a very poor family, but I did not know that at that time. Some times the expression, "Ignorance is bliss" is right on!

    Posted by Cecil on February 1,2010 | 08:22 PM

    The only disturbing thing about this article is that throughout it you refer to Mrs. Lacks as a black woman, over and over. Never, in this day and age, do you state what the author stated in her book that she was the direct product of black and white lineage (which in genetic studies might be relevant?). Many other articles acknowledge this fact when describing her and her heritage, yet the one in the Smithsonian does not mention this fact or the diverse genetic heritage of her cells.

    Posted by Sherree Meadows, Esq. on February 1,2010 | 08:22 PM

    I will never look at giving samples the same way again. I will definately buy the book. Also, this shows the importance of education. It is sad that the family was never made to fully understand the importance of her contribution. I would like to know how the family has done after this discovery and what assistance have they received as a result. Great work!

    Posted by Denise on February 1,2010 | 08:22 PM

    this is very interesting and who cares about the money is science

    Posted by alex on February 1,2010 | 08:22 PM

    i never read a whole article before... this one is so interesting that i had to read every single word in it... ;-)

    Posted by Sidney on February 1,2010 | 08:22 PM

    In 1951 I was five years of age and grew up in the community where M's Lack lived. Over the years I wouldhear off this lady from people who knew her. It is my understanding that her contribution to science is vast.
    Very pleased that she is finally being recognized for your her importance to science.

    Posted by R B Speaks on February 1,2010 | 08:23 PM

    Great Story! I will be reading the book!

    Posted by Su Harri on February 1,2010 | 08:23 PM

    Can these cells be used for clonning and grow into human?

    Posted by olympio on February 1,2010 | 08:23 PM

    Awesome article! Not only would I be interested in knowing the outcome of any legal claim the family has pursued; which in my opinion they have a right to, but I feel Henrietta Lacks should be added as a contributor to Black History in this country, along with George Washington Carver, Dr. Martin Luther King, Jr., Mary McLeod Bethune, Rosa Parks, Jackie Robinson, et al.

    Posted by marie on February 1,2010 | 08:24 PM

    Another example of how doctors from Johns Hopkins University and other medical institutions in this country experiment on poor patients without obtaining informed consent from the patients and/or their family.

    Does the end justify the means? I don't think so, and Johns Hopkins should and does know better. However, it is a clear indicator of the institution's arrogance and its lack of concern for the patient or the patient's family.

    Posted by Lynn Pinder on February 1,2010 | 08:24 PM

    Saying the first humans on the planet were black is not the same as saying that black people were the first on the planet!

    All living humans, not just present-day black people, are descendants of the first humans on the planet.

    We assume the first humans on the planet were black, because they lived in Africa and because today's San people have the oldest DNA types. But we don't have any proof about what color the first humans were!

    Posted by Martha on February 1,2010 | 08:24 PM

    An amazing story.
    Here is the book #:
    ISBN 1400052173

    Posted by Paul Owen on February 1,2010 | 08:24 PM

    The idea of "immortal" cell lines isn't that the individual cells never die. The cell line itself continues on forever. Primary cell lines, those taken from tissue and grown in culture, will continue for 50 transfers. Then they crash or die out. Sometimes, as with HeLa, the cells transform and the cell line doesn't crash after 50 transfers. Because the researchers started with cancer cells when starting the HeLa line, it is possible that the cells were already transformed. As far as the ethical questions, the doctors thought they were dealing with tissue that was going to be thrown out anyway. The technology wasn't available to really test the tissue and find out very much about her cancer.

    Posted by Jo Burman on February 1,2010 | 08:24 PM

    perfectly brilliant...I think this would be the best book can could ever read after Micheal Crichton's NEXT...I love to have a copy of this in whichever ways I can. Very interesting yet it seemed to be more than a story, it's a reality.

    Posted by kliengene bohol on February 1,2010 | 08:24 PM

    and our microbiology professor said that using humans to do research was unethical and unheard of. Thank you for bring this out into the light. I would gladly donate my whole body if someone would find a cure for FIBROMYALGIA; OSTEOPOROSIS; SLEEP APNEA; DIABETES II; ADD ADULT ONSET;OSTEOARTHRITIS; CAD; HTN;DEPRESSION, ETC., ETC., ETC.

    Posted by sylvia m. r hinojosa, r.n. on February 1,2010 | 08:25 PM

    WOW!! How can dead human cells be 'immortal'??? ?

    Posted by mindy on February 1,2010 | 08:25 PM

    This is an very interesting piece. I really looking forward to buying this book and reading it over the summer.

    Posted by jessica nails on February 1,2010 | 08:25 PM

    Having read this story,one can only imagine the possibilties that lies beneath the skin, i hope the family will be all the better for this story.

    Posted by D.O. MORRIS on February 1,2010 | 08:25 PM

    This article is excellent, but I think it could have clarified what an "immortal cell" is compared to a mortal one. I'm not a scientist, but now I'm so curious that right aftetr writing this comment, I will do some web research on the difference and significance of this particular kind of human cell.

    Posted by E. Collard on February 1,2010 | 08:25 PM

    This shows how unique everyone is and how important education is for all of us.

    Donald W.Payne

    Posted by on February 1,2010 | 08:26 PM

    somebody out there knows the truth,why missing the point.there are still spekilations regarding this matter.

    Posted by johnny botes on February 1,2010 | 08:26 PM

    Finally

    Posted by skibotex on February 1,2010 | 08:26 PM

    "HeLa" cells? Is this a hoax? Teenagers used to say something was "hella" this and "hella" that. And this amazing discovery is just in time for Black History Month.

    Please.

    Posted by Stimpy on February 1,2010 | 08:26 PM

    This is absolutely amazing I would love to read the book and I to wonder if the family was or will be compensated,they should be. I think that she would be happy to know that her death resulted into something that will help everyone and that color has nothing to do with it.

    Posted by Dottie on February 1,2010 | 08:26 PM

    hi,im 13 years old and i think this story is interesting!!!!!!!!!!!!!!!!!

    Posted by cmarier96 on February 1,2010 | 08:27 PM

    Very interesting!

    Posted by Linz on February 1,2010 | 08:27 PM

    How come I never heard of immortal human cells before. Is this for real?

    Posted by Nevis Bruce on February 1,2010 | 08:27 PM

    This shows how unique we all are as well as the importance of education.

    Posted by Donald W. Payne on February 1,2010 | 08:27 PM

    Woah! thats intresting! sounds like somthing off a sci-fi movie!

    Posted by Justine on February 1,2010 | 08:28 PM

    excellent indeed! Henrietta Lacks remains virtually unknown, buried in an unmarked grave and only known as HeLa, hope she'll be given credit for that study and so with her family...

    Posted by on February 1,2010 | 08:28 PM

    I would say that there is a lot more to this story than "meets the eye". This was exploitation by a white scientist of a poor black woman. Did he let her die just so he could "harvest" the cells. Was she specifically profiled for her suitability for research and then allowed to die? Legally, there appears to be millions of dollars which should go to the family of this innocent soul.

    Posted by D Paul on February 1,2010 | 08:28 PM

    For all the hooplah about the Lacks being poor, I notice the lady is wearing a very expensive coat in the picture!
    Also, I have very little patience with Deborah's brothers. None seemed to be interested in finding out something about their mother, even a small bit of loving memory---all they cared about was exploiting her for money! Hope they got plenty and choked on it! Very unfeeling toward the woman who gave them life! How many others did she save? How many within her own family were saved by the polio vaccine? It wouldn't surprise me if one of those "sons" didn't have a child who might have had polio had it not been for his/her grandmother, yet I'll bet the father only cared about how much he could get. Yes, the family should have been told, they should have been compensated, but, considering the time it was done, over sixty years ago, there should be no blame or censure. That's just the way it was.

    Posted by Lee Wacker on February 1,2010 | 08:28 PM

    Heaven Forbid the family should be joyful over the contribution to the World...

    Posted by K on February 1,2010 | 08:28 PM

    I do believe the family should be compensated for the use of her cells.The doctors and scientists who took the cells should have informed her and her family what they had done and offered compensation. They didn't and that is most unfortunate.They should make restitution to the family and rejoice that the outcome saved untold lives and could one day be the foundation for the cure of the very disease that claimed her life. The whole world should know of this woman and her family and how she unknowingly did so much good for so many. CONTINUED BELOW

    Posted by Nathan on February 1,2010 | 08:28 PM

    very interesting, immortal!!!! wow, i will encourage my daughter to make this her next essay project, after i buy the book

    Posted by lynn on February 1,2010 | 08:29 PM

    This well may be the only living human cells in a few years. after are greed destroys are oceans and air. its time we all become responsible for the earth. OR ELSE

    Posted by rayo on February 1,2010 | 08:29 PM

    We have HeLa cells in our cell repository where I work. I can tell you from personal experience that they are a very agressive cell line. If another line is contaminated with HeLa cells they will generally outcompete that cell line in-vitro and eventually be the only cell left. HeLa cells certainly aren't the only cell line that has this quality, but they are extremely common in research and have a wide variety of uses.

    For those who asked, an immortalized cell line is one that can be continually passed in culture. They are grown in a monolayer on the surface substrate of special culture flasks or plates. HeLa cells are what are referred to as anchorage cells. That is, they anchor themselves to the bottom of the flask and spread out until there is no more room to grow. Once they reach this point they must be disassociated (lifted off) the flask surface by either a chemical (generally tripsin versene) or by physical means. They are then placed in new culture medium and a new flask. Each cell line has different nutritional requirements and a specially designed growth medium which induces optimal growth.

    Posted by Jackjack99 on February 1,2010 | 08:29 PM

    Amazing!!! I agree that the family of Lacks should be compensated from whatever the scientists got from using her cells.

    Posted by Migs on February 1,2010 | 08:29 PM

    People, don't be naive. The true hero were the scientists and biologists, not Henrita. Though her cells were exceptional and helped science without her knowledge/consent, but scientists who did this deserve a lot of credit.
    It is really misguided for some here to suggest that Henrita's family should sue the scientists.

    Posted by Atul on February 1,2010 | 08:29 PM

    Lawsuit Moore v. Regents of the University of California, is a Supreme Court of California case decided in 1990 which explains why the family of Henrietta Lacks will most likely not receive any money even though the taking of the cells was a wrongful act. As Beth mentioned, the court held that an invidividual has no property or ownership interest in their cells or biological tissue after they are removed or discarded from their body.

    Posted by mba on February 1,2010 | 08:30 PM

    There's a very good article with a lot more information on this story (taken from the book, of course) in the February issue of Oprah magazine.

    Posted by Marge Nichols on February 1,2010 | 08:30 PM

    CONTINUED From above...
    The issue I have here is the blatant ignorance I have seen in the comments above. How can anyone be so ignorant as to try and make this an issue of race. It is people like that who keeps racial issues alive. Only someone who is racially biast would think for a moment that the taking and use of her cells would be racially motivated, How stupid could someone be? To take something so miraculous and turn it to something ugly. I am appalled and outraged at the blind negativity displayed by such uneducated and ignorant people. The year is 2010 there is no man or woman alive today who experienced slavery first hand. The civil war ended in 1865 that is 145 years ago I think that is more than enough time to move on. For God's sake we have a black president how can a country that is suposidly so anti black accomplish this unless we have inndeed over come this issue and become blind the the color of a mans skin and focus on the man and his attributes. Enough with crying racial bias dont take what contribution this woman has made to our society and tarnish it with bigotry and hate. She should be commemorated and honored as a heroin. Name a scietific building after her or better yet an entire university devoted to sientific research and erect a statue of her in the front of it. Award her the Nobel Prize allow her family to morn the loss of thier loved one and take pride in what the Family name means to the world. But please don't mock her and undermine all the good done by using her as a platform for your hate filled rants about "the evil white man and how he is constantly trying to put down and harm the black man". Racism only exists if we allow it, Stop giving it life by throwing at the world. Stop spreading your messages of hatred allow this woman and her family the peace and dignity they deserve.

    Posted by Nathan on February 1,2010 | 08:30 PM

    Did anyone ever question if the husband gave her the health problem she died from? Or is that irrelevant?

    Posted by K on February 1,2010 | 08:30 PM

    Bravo Henrietta.

    I have worked with HeLa cells in my researching past, (and no, I didn't earn a penny of profit from the labor). I tried, like most researchers, simply to push back some of the obscuring curtain from the marvel of cell biology. When I started working with HeLa cells, I was told the 'Helen Lane' story. It is nice to finally put a correct face and name to an enormous contribution.

    While I cannot condone the manner in which the cells were obtained, I note that my concern today is with a 1950's science which still had much to learn about ethics, patient confidentiality and intellectual property. It is truthful to say that Henrietta taught us many of those lessons herself!

    The contributions made by Ms. Lacks to the understanding of human biology and the diseases that plague it, is staggering. And I am especially pleased to note that it was a black woman who did so much for humankind. Such contributuions need to be heralded.

    While her contribution is profound and unique, I hope that the book also lists the commitment and perserverence of the scientists who nurtured, fed, stimulated, interrogated and analysed the cells. The Salks, Sabins and thousands others who poured their intellect and imagination into solving these problems, and could count their success on the information that only Ms. Lacks could give.

    It is truly an American position to talk of compensation. I just hope that the conversation also inculdes what is truly due: the abject wonder, respect and appreciation from the entire world for Henrietta Lacks, and for her contribution to the well being, general health, education and longevity of the human race.

    Thank you Henrietta, you have taught us countless lessons, using just the very nature of you, your cells.

    Posted by Dr. Gregg A. Adams on February 1,2010 | 08:30 PM

    Well said JLP. That doc would have been sued if he dared do that nowadays, as well he should be. My father died from congestive heart failure and I was warned by my family that the doctor may ask my permission for samples to use for students to study and to be careful not to sign ANYTHING I did not agree with. I know my dad did NOT want to have any part of him donated to science, so when I was asked, I said "NO." If my grandchildren found out, through some twist of fate, that my father's cells were indeed used without family permission. I would hope they'd sue the pants off of whomever was responsible. Doctors take an oath. This doctor was way out of line and regardless of the benefits, Henrietta's family should receive some form of compensation. Her cells were NOT DONATED, they were taken!

    Posted by hello on February 1,2010 | 08:30 PM

    W@w!
    "Take note" Ron Howard/ Clint eastwood..
    Can't wait to see this at the show!

    Posted by PineNuts on February 1,2010 | 08:30 PM

    Henrietta still has a voice,and lives on ...in a echo in our hearts and minds! We are boren to make a difference in LIFE! NO MATTER WHO WE ARE. I think it's amazing that so much has been learned from one person,but her family should of knew all but to clear what was going on.It was wrong what happen and I hope the family is at peace now,and finance well. Thank you for letting us know the truth

    Posted by Renee on February 1,2010 | 08:31 PM

    It,IS... SO MYSTERIOUS ON OUR LIFE INCLUDE SCIENCE CAN NOT EXPLAIN

    Posted by Mauro Pena on February 1,2010 | 08:31 PM

    Great story. However, I'm sure that the fact that this family was poor and black contributed to them not being compensated for this great contribution to medicine. It may have changed the course of this families future for generations. J

    Posted by JBM on February 1,2010 | 12:33PM

    ??? how if it never happened they be were they are now and what do you think happens to all that blood you give ?

    it gets tested and if they find some thing they think is useful u think they will be calling u with a check, black or white or red or yellow hell no besides its as cell and if it saves lives why do the feel the need to make money on it and it wasent even them it was the mom!!

    Posted by errin2cr@yahoo.com on February 1,2010 | 08:31 PM

    Simply amazing. =)
    An interesting article that's for sure.

    Posted by Anya on February 1,2010 | 08:31 PM

    This is an incredible Story.Being in the Medical World to me it is awesome to be able to put a name and face to something as important that HeLa was to us..

    Posted by Very Interested in Oklahoma on February 1,2010 | 08:32 PM

    They should give the guys the money.

    Posted by BLoo on February 1,2010 | 08:32 PM

    This sounds amazing where can i buy the book im only 10 and i think its something my class will surely like it. like love!!!!!! exept its sad she died and her daughter part and everything.WITH NO MEANS I WILL BUY THIS BOOK!!!! IM SO EXCITED TO BUY THIS!

    Posted by CCS on February 1,2010 | 08:32 PM

    interesting and haunting! :)

    Posted by carolyn flores on February 1,2010 | 08:32 PM

    Excellent story about Henrietta Lack. I hope her family was compensated well for Henrietta's contribution (although unknowingly) to science and to thousands of people who were in need of a medical cures for various diseases, even those that baffled many doctors & scientists. Yes, it was wrong what this doctor did, but in the end it has helped all of humanity. Another example of doctors taking what they want is the placenta from after birth which is used to make collagen creams to restore usefulness to the skin, put in lotions and "no" the patient is not given a discount from the hospital fees. Again, excellent story.

    Posted by Sheryl on February 1,2010 | 08:32 PM

    This is an incredible story! I want to read the book now.

    Posted by ListenToLeon on February 1,2010 | 08:32 PM

    Great story!!! But, some people are going to read this peice and scream "Racism"! Think about it, no matter how anyone describes a person of color, people are going to find something to complain about! In the 1950's, people of color, whether they be black, Spanish or American Indian, anyone who had a darker skin coloring, these people were considered not human or savages! In the '50's, there was segragation!! So, the only way scientists could study people of color was to "Steal" their tissue samples. Non of these scientists concidered that what they were doing was wrong, there were no laws to protect people of color back then. I'm just glad that this story is getting out now and Henrietta's family can be compensated for the wrong that was done. The Laws of today are so very different from 1951! The human body is an amazing machine!!! It can replace itself completly in so many years.... amazing!!! The book can probably be found in any Walden's, Borders or Amazon.com. I know that I'm going to get the book!

    Posted by Brenda on February 1,2010 | 08:32 PM

    Wow! I am buying the book. Fantastic story.

    Posted by qt8625 on February 1,2010 | 08:33 PM

    hi,im 13 years old and i find this story very interesting!!!!!!!!!!!!!!!

    Posted by cmarier1996 on February 1,2010 | 08:33 PM

    When they talk about the USA falling behind the rest of the world in science education, you only need to look here to see it proven. Eighth graders in most countries would know more than the typical commenter on this board. There have been a few intelligent comments, but most of them are drowned out by ignorant, childish discussion.

    Here is a summary of some facts:
    -All cancer cells are immortal.

    -Tissue samples were treated with less care in the past.

    -The USA was much more racist in the past.

    -Henrietta does not seem to have been denied any care as part of a medical experiment, unlike the Tuskegee participants.

    -Henrietta probably got inferior care because she was Black. Obe cannot know in this case if she got care that was inferior to what Whites got or not, but it's likely based on statistics.

    -Although this article chose to shine a spotlight on her, it was the work of the scientists who made the cell lines worth billions of dollars.

    -Medical waste is just waste. Trash. No one stole anything from Henrietta. If some scientist went through the landfill and discovered something in there that would magically turn lead into gold, do you think that you ought to be entitled to a portion of the proceeds because you once had the item in your house and chose to throw it in the trash?

    -The billions of dollars spoken of in the article represent the net commerce resulting from the cells, not the amount of profit that went into someone's pocket. That means nurses, doctors, professors, janitors, CEOs of companies, book writers and publishers, and people from every imaginable profession got part of that money. Probably no one person made a fortune from this line of cells.

    -To 90% of the posters, if you're still in school, please stay in school and get more education. If you're out of school please make sure that your children get a better education than you have. Ignorance is like a flabby belly, no one really likes to see it on display.

    Posted by Itsme on February 1,2010 | 08:33 PM

    I let my 5th grader read this article and she was fascinated. You have given inspiration to a generation of people with this article. Let me know where we can get the book.We both will be reading it. I hope the family was or will be compensated.

    Posted by Dett on February 1,2010 | 08:33 PM

    If they have been doing this for all these years, Why haven't they come up with cures for Cancers, HIV,etc..? Unless they have and the government won't let them because this would stop the thinning of the human race. If they haven't come up with cures now after all these years they never will. You can't play GOD, only GOD plays GOD.

    Posted by Angela on February 1,2010 | 08:33 PM

    I learned about HeLa cells in many of my undergrad biology courses. They are of utmost importance in the biological community. It's nice to get a delicate overview of both sides of the story. What's the point of going into science if you don't consider the lives touched by your research?!?!? Nice article!

    Posted by Domonique on February 1,2010 | 08:33 PM

    I wondered and wondering, what was)is she thinking, the attitude towards life, does she have an attitude of life is immortal while she`s living, meaning before she died phsically

    Posted by Ooi on February 1,2010 | 08:34 PM

    Thanks to the contribution of HeLa, my granddaughter (now age 3) is conquering childhood cancer. This is about so much more than money -- I'm sorry her family feels that it is all about money. Thank you St Jude for prayers answered.

    Posted by Janie Stone on February 1,2010 | 08:34 PM

    Johns Hopkins Hospital in Baltimore,Md. should compensate Henrietta’s family for their creation of “the first immortal human cell line”, from their mother, which developed many scientific landmarks, including a cure for polio, cloning, gene mapping and in vitro fertilization.

    There must have been a paper trail to follow the sales of her cells to various laboratories, and to follow all the pseudonyms that were created to cover-up the trail of deceit. They should honor her for her contribution to science and the neglect I'm sure she received as a black woman during that era.

    The story didn’t mention how & when Henrietta died and if she was ever cured or treated for her illness; or just used for a science experiment?

    Posted by Tekladie on February 1,2010 | 08:35 PM

    Taken something without permission is stealing, whether it's a pen or someone's lunch you stole out the frig at your job(alot of that going around), let alone a CELL. Henrietta's family is owed sooooo much money. Her cells were life saving and still are(God bless her). I feel that, the story should've come out in 1951 and the family should've been compensated as the BILLIONS of dollars poured in. Stealing with good or bad intentions is never right. ONLY IN AMERICA. ITISWHATITIS.....

    Posted by Gee on February 1,2010 | 08:35 PM

    GENIUS

    Posted by Courtney Davidson on February 1,2010 | 08:35 PM

    i hope the family of Mrs. Lack will get what they deserve sooner..

    Posted by Venus on February 1,2010 | 08:35 PM

    Very intriguing, I am very interesting in this book. I think the family should be compensated.These scientist or labs were/are selling the cells.

    Posted by eileen on February 1,2010 | 08:35 PM

    This is fascinating and would like to see a movie made. I'm in the middle of a genealogy hunt for my ancestors and would love to find out something like this about one of my relatives. I do believe the family should be compensated only because they took the tissue without telling Henrietta or her family.

    Posted by Benjee on February 1,2010 | 08:36 PM

    I am also scientist, and I have used a lot this HeLa cells. I knew a little bit of the history of Henrietta, but now that I hear the whole story, make me think that it should be fair that her family have economic compensation. I think that for those who make business with the cells. Maybe, for example, the ATCC (American Type Culture Collection) who produces and sell the cells, could add an extra cost to this cells when sell them, and this money to be used just as a help of her family.

    Posted by Manuel Ramos-Kuri on February 1,2010 | 08:36 PM

    Henrietta's family should be proud of their mother's contrubution to humanity. In the 50's there was no consent for tissue going to the lab and I would think most of it went for research otherwise, why send it? This is not a black/white issue, please do not make it one. The point is the mystery of where HeLa cells came from is now solved. If it were my mother, I would be proud that she was able to save so many lives. Henrietta died to young but she left the world a great gift. She didn't sign a formal consent but the scientists didn't single her out to steal her cells to make millions of dollars.
    Let us honor her, not fight over the past we can not change, or the compensation some feel they are owed. I would like to believe Miss Henerietta would have gladly allowed her cells to be used for such a great purpose.

    Posted by J C Anderson on February 1,2010 | 08:36 PM

    Yes the family should get some compensation. It is unfair for companies to make money off of this woman's cells and the family to get nothing.

    Posted by S. Hood on February 1,2010 | 08:36 PM

    Thank you for this piece.

    Posted by Link Starbureiy on February 1,2010 | 08:36 PM

    This story make me so emotional.I deffinitly will buy this book thank you

    Posted by Maria A Lopez on February 1,2010 | 08:36 PM

    Paying this family for a cell sample opens the door to: if someone get compensated for a cell sample, how much should the family of a deceased organ donor get paid? There is nothing really special about the HeLa line, cell samples from other people would work as well. All of us getting Pap smears are giving cell samples.......

    Posted by cookie on February 1,2010 | 08:36 PM

    This story is amazing, can you tell me the name of the book. I would read it

    Posted by kim on February 1,2010 | 08:36 PM

    GREAT ARTICLE, I AM GREATFUL FOR HENERITTA'S SUPPORT TO MEDICAL RESEARCH. I AGREE THAT WE ALL SHOULD SUPPORT FINDING NEW CURES FOR BLACK GENETIC RESEARCHES, THERE ARE NUMEROUS MEDICATION THAT DOES NOT WORK FOR BLACK/ MIXED GENES. THERE ARE SEVERAL MEDICATION MY BODY REJECTS . I CREDIT IT TO GENETIC DEVELOPEMENT,. MY DECISION IS FAVORABLE FOR RESEARCH. I WILL SHARE THIS INFORMATION AND SEARCH FOR THE BOOK. job well done

    Posted by deloris milton on February 1,2010 | 08:36 PM

    I think as this article points out, since her cells have been used as the foundation for so many cell based technologies that, we are all linked by DNA/Biology. Unfortunately, due to some missteps by government medical research such as Tuskegee, many people of color don't trust modern medicine. This is unfortunate as, it doubled the human life span in the span of 50 years or so due to anti-biotics and other technologies, stem cell research and many other technologies will likely extend our lifespans further. However, countless people die needlessly every year, simply because people do not donate their organs, when they die. over 50% of those on the waiting list to receive organs die before even getting their organs, due to this. That is more than due to complications during surgery such as infection, the person being just too sick to deal with the physical stress of surgery, and rejection combined. The largest group who don't sign up to be organ donors is the same as those who don't sign up to be blood donors, and that is people of color. This is true for all forms of biological donation from bone marrow, to platelets. If everyone in society signed up to be donors, there would be no shortage of organs, blood, or any other item needed. Hopefully, this story will help readers learn what they can contribute to medicine, and their fellow human beings. I myself am already a living donor, I donated a kidney to a cousin in 2000.

    Posted by Ernest on February 1,2010 | 08:37 PM

    the pollo vacine dosent work its us bs they havE never proven it to prevent pollo WAKE UP AMERICA STOP BEING SEEPLE TO THE LIES

    Posted by eredy on February 1,2010 | 08:37 PM

    Very interesting article. I hope her family was compensated! I want to buy the book now!! God Bless

    Posted by cyndi on February 1,2010 | 08:38 PM

    Great article. I was wondering is her cells are the only know cells on record that never perish? If so, what is the most likely reason that that is? Thank you. Best of luck with your book. Im sure is a great one.

    Posted by Ansel on February 1,2010 | 08:38 PM

    I wish the catholic church can also make a study. she might become a saint like other saints whose body is still intact after many years..this is an argument between religion & science

    Posted by nona corazon a. siojo on February 1,2010 | 08:38 PM

    Very interesting article and i have to buy the book and read the whole story!I just want mention that the Family should get compensation!

    Posted by W.A on February 1,2010 | 08:38 PM

    UNBELIEVABLE??

    I think not, what everyone is ignoring, is that in the South, during the early part of the Century, experimentation on Blacks was common ground. There are too many stories like this,only they didn't end on a positive note!

    When I was a little girl, my mom told my sisters and brother of a local store owner, was well known in the Charlotte brickyard area, for experimenting on anyone with a deformity, (mole, extra finger, limp etc.. The poor (both black & white) knew to STAY AWAY! The word around town was, if you were poor and had some kind of skin, hair, problem, missing a limb, had an extra limb anything of scientific curiosity, or some sort of disabilty, then you or your loved one had better STAY AWAY FROM THAT STORE!!! If you went in with an ailment/disability/handicap or sickness, you NEVER CAME BACK OUT.....ever. We were told the owner desired all of his life to be a Doctor, but didn't make it.

    True or False? Was it right? Did it happen? How could it happen? Come on people,get real.....it is still happening even today, we are talking about HUMAN BEINGS (messed up creatures in our universe) who in their pursuit of Scientific BREAKTHROUGHS" will do just about anything and justify the end results, as the author is seemingly doing in her book.

    So whether her family was or was not compensated, whether there was great technological breakthroughs, doesn't really matter because it will and does continue even up to today, probably going on in HAITI as we speak. But that's just my lil ol' opinion. What do you think?

    Posted by Atheus on February 1,2010 | 08:38 PM

    The drug companies made many-many BILLIONS of dollars selling medication to people. Medication that was invented through this woman. They "WILL" make BILLIONS more. There is no reason "other than greed" on the part of these companies, that they don't give her family some money. It would not have been possible without her, and I think they owe her family something! If it benefitted mankind all that much, than why not give the family something "just as a way of saying thanks?" I wonder how much of her tissue they took. They sent some into space,used it for polo, for cloning etc. etc. They've been using her tissue for all these years. It sounds like they took a lot of flesh from her body.

    Posted by suann on February 1,2010 | 08:38 PM

    I just wanted to gawk at the ignorance on this thread. I don't think it is malicious ignorance, but a lot of posters seem not to know the history of the U.S. when it comes to testing, and unethical medical behavior to poor people an minorities. Heck the birth control pill was first tested on Puerto Ricans. These test (or in this case harvest) were conducted w/out consent or even knowledge in most cases. Eugenics was actually started in this country and the landmark Eugenics case was actually on a poor (Appalachian I believe) white woman. Also, if you read the book (which I recommend) you will find out the also test on her kids (in the 70's) and did not explain a lot of stuff to them.

    Posted by eh on February 1,2010 | 08:39 PM

    Maybe the researchers who took Henrietta's cell do not owe the Lacks family any money but what about the multi-billion dollar businesses who earned and profited very much from the said cell, didn't they suppose to give back even a small part of the money they earned to the Lacks family? I personally feel that this situation calls for a very thorough study and that the lacks family should get what science owe them.

    Posted by Renato Cañaveral on February 1,2010 | 08:39 PM

    Did you research the notes from the scientist on this? Why did he decided to use her cells? Or did they take cells from others which did not live? Lots of questions here...

    Posted by on February 1,2010 | 08:39 PM

    Whoa!!!! I've heard about the HeLa cells, never knew from whence they've come. I must purchase the book. I sure hope the sons and daughters receive restitution

    Posted by Latrice on February 1,2010 | 08:39 PM

    Buy the book if you don't see the bigger picture here. It isn't entertainment. It sounds like a comment on health care. There is a situation before the country today and that is pulic universal health care. You will have a better chance of seeing a doctor and getting your cervical cancer treated than the chance of being used by some unethical health care worker with other objectives such as filling his pockets with money doing his own unsupervised frankensteinal research if this country decides on a universal health care system. Add this story to the one where the doctor used his own sperm from his sperm bank to impregnate over 30 women with his own children. Did you notice where the Health Care is on the Monopoly Board? Sure it is! It's under the Take a Chance cards!

    Posted by James Roossien on February 1,2010 | 08:39 PM

    That was nice, very interesting.

    Posted by JenEm on February 1,2010 | 08:39 PM

    Evidently the internet ate my comment.

    While much has been made of the Lacks' family's poverty, I noticed the lady in the picture, evidently Mrs. Lacks, is wearing a very expensive coat.
    I have very little patience with her "sons." Nothing was said about them wanting to know more about their mom, not even a small, loving memory---all they said was "gimme!" I wonder if they appreciate how many children their mom saved, how many were in their own family? I do agree that they should have been told of the procedure, but the same thing happened to me in the sixties, so who am I to condemn the doctors or the family? Compensation, within reason, should have been paid--yes--but I would lay odds the family demanded enormous sums, and I have the feeling their mom would not have been pleased! Another item, although many of you are decrying the "taking" of her cells, don't forget--this was over sixty years ago, and in the case of cancer, no one was told--my family is white, yet when my aunt died of cancer, no one said anything to the family, but her entire tumor was sent to the lab. Don't ask me why. Don't know, don't care. Back then, things were done very differntly than now, mainly because people now are far too interested in litigation.

    Posted by Lee Wacker on February 1,2010 | 08:39 PM

    Where can I buy the book? Confusing, but sounds God want to remind the people that He is really great and His LOVE NEVER DIE... NOTJING IMPOSSIBLE FROM ABOVE.

    Posted by chat on February 1,2010 | 08:39 PM

    Fascinating story! Though I do have to differ and state that neither she nor her family is entitled to compensation (see Supreme Court ruling in Moore v. Regents of the University of California). And I'm apalled at the people who denegrate Dr. Gey for using her cells. He did nothing that was illegal or unethical at the time, did not patent her cell line, and in fact helped save thousands of lives because the cultured cells were used to develop the vaccine for polio, among other medical breakthroughs. If it hadn't worked so well her family wouldn't be clamoring for a piece of the money now, as if it were proceeds from copyright.

    Posted by krazychemist78 on February 1,2010 | 08:40 PM

    Very interesting article. Too bad the race card has to be thrown in the mix even here. Sheesh. We're all human. Thanks for a great article.

    Posted by Fred on February 1,2010 | 08:40 PM

    Wow what a increditable story! Very interesting..It definitely caught my interest on how someone's cells can be immortal..I really do hope that the family did get compensated and I eager to learn more..

    Posted by Christina J on February 1,2010 | 08:40 PM

    This is a great story. I loved the part where the daughter finally learned a little something about her mother. However, I do believe the family is due some type of compensation because they took the cells without permission and used them to create not only research and answers to medical questions, they also used them to make a great deal of money. If she had agreed to "donate" them, then it would be a different story. However, this woman nor her family had no idea what had happened and I believe it would only be fair that they receive something as compensation due to the fact that they took them without permission; therefore,they were not given but stolen. It is more about justice than the almighty dollar. Please let us know what happened when the family tried to obtain compensation.

    Posted by Beli nda Folger on February 1,2010 | 08:40 PM

    Thank for this,i would like to know more.Where can i find more on this subject.

    Posted by J Edward Powell on February 1,2010 | 08:40 PM

    What a great start to Black History month. This article reminds us that we humans are all connected. Peace.

    Posted by J on February 1,2010 | 08:40 PM

    I think it is a wonderful story, too. People should not get too bitter about it; the fact that the name and identity was hidden was a part of American history and we have to see it like that. Not all history is supposed to make us feel good. Bravo to the author. In terms of historical context: most whites would not have been happy to have a "Negro" cell at that time, obviously the scientists knew there was no "negro cell" to worry about. That is why the name was hidden, though. I do hope the family got some compensation though, that would only be fair. Just goes to show humans are humans, no matter the packaging! I'm glad we have moved so far that most comments are positive ones. I am sad too that this woman died so young, and sad that her daughter could not know her. Money of course is important, but no money can replace a loving mother.

    Posted by Wendy Wilson on February 1,2010 | 08:40 PM

    WOW! This was a very interesting story. I really cant wait to learn more about this story. I really can't wait to get the book. This story is so on time for Black History Month! WOW! WOW! WOW!

    Posted by tamora on February 1,2010 | 08:41 PM

    wow

    Posted by amy chen on February 1,2010 | 08:41 PM

    Since so much money has been made of off this one particular cell-line, it seems like someone could scrape together something for the family. But as to a right to money for your cells, no way. Without the education, knowledge, labs, equipment, etc, etc, etc., those cells are worthless. You have no more right your loose cells than you have a right to the leaves from your tree that land in your neighbors yard. If you cells are so valuable, why do you leave millions of them in you matress for dust mites to feed on? Let's sue those dust mites!

    Posted by Michael Honohan on February 1,2010 | 08:41 PM

    Exactly; cells are not immortal, they have the capability to multiply and hence become "immortal". I think it is a fascinating story, the history behind something like the HeLa cells that changed science. However, I think the conlcusion is weak; it's obvious people should have the right to donate or not to donate their cells, but it doesn't matter what happens to them...they're cells! cells are not the living person...why does the author say that people have "thoughts and feelings about what happens with their tissues"????? That's beyond the point and doesn't matter. The point is that many of those tissue are used to save lives.

    Posted by J Rivera on February 1,2010 | 08:41 PM

    Interesting Story

    Posted by Craig on February 1,2010 | 08:41 PM

    I wish I could live for ever

    Posted by hey on February 1,2010 | 08:41 PM

    There are a few things in life that pique my interest a lot. This is so intriguing that I will go to browse for the books and read it front to back. WOw!

    Posted by Nancie Broooks on February 1,2010 | 08:42 PM

    There has to be considerably monetary issues here - those cells belonged to her and her estate - and where used in many enterprises that generated not millions but billions for people. The family should get a good IP lawyer.

    Posted by tom on February 1,2010 | 08:42 PM

    THIS IS A WONDERFUL THING IF IT IS USED IN THE RIGHT WAY THAT BENEFIT THE HUMAN RACE,ON THE OTHER HAND HER FAMILY SHOULD GET COMPENSATED IF THERE IS ANY PROFIT INVOLVE FROM THE SALES.

    Posted by ANTHONY CLARK on February 1,2010 | 08:43 PM

    This article should be mandatory reading for all African Americans this month.

    Posted by E. F. Williams on February 1,2010 | 08:43 PM

    If Henrietta was at the hospital for treatment of her cancer, then as soon as the cells left her body, they were the property of the hospital, according to the current laws. These laws were put in place in case, say, a kidney donor had second thoughts after the transplant, or something like that. Several cases, Henrietta's included, are forcing people to question these laws, so there is hope.

    Posted by Simon on February 1,2010 | 08:43 PM

    I just have to say to some of these people posting about her cells being stolen and how her family should be compensated instead of letting some white scientist get rich off it. We are all enriched by the work that was done with these cells, not just some scientist. People are not entitled to money no matter how much they may salivate at the idea of getting rich quick. The payment one should receive from that is pride that something about their genetics have helped people the world over. With that said . . this is one awesome story although I wonder how much truth there is about cells floating around on pieces of dust . .especially living cells that are able to reproduce.

    Posted by byron on February 1,2010 | 08:43 PM

    Absolutely fascinating. Let's see if Oprah climbs aboard the band wagon and pushes for recognition of this woman's unheralded contribution to science. Who better to press the issue of social injustice if in fact such an injustice was committed. JMHO

    Posted by Ken Metal on February 1,2010 | 08:43 PM

    Very interesting article!!! I don't think that they exploited her because she was black. I think it was done because she didn't know medicine, just like they could do it to anyone & if you don't know what questions to ask, you would be in the same predicament I hope to get the book when its available from the library. Hope the family was finally compensated & I am thankful that research was done, even if its beginning was shaky...I'm sure Henrietta's cells saved lots of lives!

    Posted by KLR on February 1,2010 | 08:44 PM

    Has anyone thought to dig up her body & check & see if she's decomposing or not? Obviously her cells can still reproduce after her death...

    Posted by Kristin B on February 1,2010 | 08:45 PM

    Paperz said it all. My God. What do they do with our tissue when we have surgery? Read the fine print. Don't give up the rights to your body's tissues.

    Posted by Mihele B. on February 1,2010 | 08:45 PM

    Very interesting writing. I will also like to buy the book. I cannot even begin to imagine the extent of her contribution to science. In regards to compensation, what more compensation can there be than to know that a member of our family has helped save millions of lives, and is still helping science and medicine better our world. Her name should be in History books, everyone will know her, that will be all the compensation needed.

    Posted by Janet on February 1,2010 | 08:46 PM

    As one who oversees a medical research program, I assure you that we make every effort to ensure that researchers follow the rules, i.e. informed consent process is monitored, studies are audited, scientists must take training before they ever start the study. The Nurembourg Trials and the Tuskegee Institute Studies are a couple of examples of why it is so hard to get research approved now. If you are really interested in research, google these two topics and you'll find some really bad people did some truly awful things in the name of "research."

    Posted by shutupandplayball on February 1,2010 | 08:46 PM

    I am very thankful for the advances in medicine that were made using these cells. While I very much agree that the family of Henrietta should benefit from profits made from those cells, I also feel that it should not be forgotten that these cells were taken in the interest of science not racism. The story may have been covered up because the advances came from "black" cells, but the fact is that all races benefited. Thank you Lacks family! I'm very interested to hear "the rest of the story"!

    Posted by CB on February 1,2010 | 08:46 PM

    it's very interesting.... heheheheheh

    Posted by ivy on February 1,2010 | 08:47 PM

    Well done.

    Posted by Dan West on February 1,2010 | 08:47 PM

    Very interesting story, i would love to read the conclusion of it, so many unanswered questions in mind. I agree with one poster that said that they believe this should be posted in history books, however i don't agree with the posters thats saying the family shouldn't be compensated. If we look at this in todays world, people are paid for researches done on them and they get permission before research is done, why couldn't Henriette Lack have the opportunity to consent and even make a decision to have any profits to go to her family if she didn't live in the event that scientist profit from her cells in this way her family would have been early compensated and even been able to get a better education earlier in life. All you who say the family shouldn't be compensated need to put yourself in this family shoes but no you probably can't because you probably already have money and feel like you are above these people. But remember you wasn't always on top or where you? Then this is why you are so heartless. Afterall, her cells are still alive and scientist are still profiting from her cells so why not let the family be compensated.

    Posted by M.A.C. on February 1,2010 | 08:47 PM

    This is amazing. This is something that scientists have been doing for years. Everybody is different. Every cell is a blueprint of life, no matter who or where it comes from. This is HISTORY and something that should be talked aboiut in schools. History classes and science classes. Look at cancer, HIV, HPV, etc...its needed for research. Great article and I will get the book.

    Posted by Hollywood.Gurl on February 1,2010 | 08:47 PM

    I am the last person in the world to claim racism.. I always hate it when people play the race card...but I've gotta tell you... the "scientists" involved in this story were the most racist, self-serving, wrong headed people in the world!!! Taking cells without permission and/or compensation is wrong.. I'm tired of socialists saying its fine as long as it serves the "greater good". No, it's NOT ok.. its NEVER ok to exploit someone for your own glory and money... especially not the poor and ignorant... I'm hearing way too many white rich people chime in here not having a clue about the great evil that was done to this woman and her family. Just because its "for science" doesn't make it ok!!! It was wrong, it was racist, and it was unethical and immoral. And yeah...when you're poor ...money matters...anyone who says it doesn't, has never been truly poor, where you wonder where your next meal is coming from or how yer gonna pay yer bills..

    Posted by jenne on February 1,2010 | 08:48 PM

    how were her cells different than others did a chemical addition make then last longer did she have the type of cells that are X that if longer, they have extended life spans? Can you tell me more scientifically about this. What were they able to do with her cells and how did it help humanity? Julie

    Posted by julie hearn on February 1,2010 | 08:48 PM

    Geez, everything is about race, isn't it. Doesn't matter that this woman contributed significantly to science (and BTW, it wouldn't have been revealed any earlier even if she was white because they just didn't do those things back then). I've known since I worked with them in research in the 80's that they were from Mrs. Lacks and I didn't care what her race was. It never even occured to me to ask. It didn't matter. Wouldn't it be nice if it didn't matter to anyone, and she could be remember for the great contribution to science her discarded tissue matter made, regardless of her race. But there are those on this comment board that seem hell bent on making it an issue. Sorry for you that it makes a difference.

    Posted by Kasey on February 1,2010 | 08:48 PM

    "Posted by Paperz on February 1,2010 | 02:00PM

    Ironically white Americans were unaware that a Black womans DNA was being used in vaccinations that Im sure the majority of Americans received. I think that's the reason for the secrecy."

    It wasn't Henrietta's DNA that was injected to combat polio. Various forms of the virus was used in experiments with HeLa to determine which form of the VIRUS was effective to prevent infection.

    Nice try to stir up the race pot.

    Posted by Alcmena on February 1,2010 | 08:48 PM

    What gets me about this is the fact that these "poor black farmers" are wearing a nice suit and a mink stole. As an employed white person in 2010, I have neither and consider myself to be doing quite well. Life was obviously better in 1951 and I would have liked to have known these people. I would have worked for them for room and board. Happiness has no monetary value, regardless of what rich folks say, either white or black or anything in between.

    Posted by Paul on February 1,2010 | 08:49 PM

    my sister's stem cells were harvested after her stage B diagnosis of breast cancer. this was done before her bone marrow transplant. two years later, as she faced imminent death, her original oncologist contacted her and asked if she wanted to take another shot at another bone marrow transplant. he had kept her original stem cells in whatever manner in typical of this type of situation. granted, he was very honest about her chance for survival, which was quite low. she turned down this offer and died a terrible death. however, i believe that her doctor still has those live cells of my sister. what he may or may not do with them, i have no idea. but, my insticts tell me he would honor her cells as he honored my sister.

    Posted by cecelia latoof on February 1,2010 | 08:49 PM

    two things I hope from this story.... one, i hope scientists can clone our bodies and mind so some of us can live forever..... and two, I hope the Lacks family recieved a s**t pile of money for Henritta's unique cells....but neither of these things will happen....

    Posted by Thomas Bean on February 1,2010 | 08:49 PM

    W O W!!! This was a great piece! The book should be made into a PBS DOCUMENTARY that would inform people of this marvelous con-tribution made to our medical field. Thanks, YAHOO, for putting this up for your subscribers.

    Posted by Kathy Dutchess on February 1,2010 | 08:49 PM

    I really enjoyed this piece. I also think that the scientific world should have compensated the family for the use of these cells since they became so valuable. Especially since they were taken without the consent of Henrietta and/or her family. In the human aspect of it - the contribution was valuable with an amazing outcome. I wish there was more of the story here but I will have to get the book which I certainly don't mind.

    Posted by Linda on February 1,2010 | 08:49 PM

    Stem Cells you could also say are immortal and the body is full of them. but with All the Toxins attacking them like Pollution, and the Foods we eat, the products such as Aspertame in soda, Aluminum in deoderant, & Flouride in toothepaste. Also inhaling fumes from cleaning products. Little by little, day by day, year by year, from generation to generation. Constant bombardment cause chemical imbalances in the body than evolve exponentially in the bloodline & genes. shortening the life of stem cells therefore us. I don't know how long this womans cells are expected to live but stems cells have been said to have a lifespan of about 800 to 1000 year. Which leaves us with the question... why are we ageing so fast? "dying." Why?

    Posted by Chris on February 1,2010 | 08:50 PM

    This was such an interesting article. I will be sure to share this. Thank you!!

    Posted by BR on February 1,2010 | 08:50 PM

    Why does it matter if they are black,white,chineese,spanish...?Hello it's 2010!!all you always hear is race.An American womans cells!the story was very interesting.Because of her genetic background(black)it now seems by reading most of the comments that is one of, if not the most important detail of the story.another freedom/right stolen from the black man by the (white)man.by saying this I'm now probibly being considered/labeled a racest.I was raised by my immogrant grand perents,have been overseas,lived in all four corners of the U.S.and see how closed minded Americans can be.your now reading proof!I've been called honky,cracker,whiteboy,blue eyed devil,ect...and probibly now will hear more.and thats racest!my family never owned slaves.we came here in the 1970s.I now live in the southeastern U.S and hear the race thing constantly.and from who?90%of the time blacks.English is my second language and not my best.so if I offended someone I apologize my english is still not flawless.I hope for a day when the occomplishments of a person are praised for what they are and not who they are.

    Posted by ken on February 1,2010 | 08:50 PM

    Captivating! Broad stroke of wrongs to women of color yet how they have helped mankind! Hope the family is compensated and more of this mystery is revealed! P.S. Forever hasn't happened yet!

    Posted by Kris on February 1,2010 | 08:50 PM

    This is very interesting. There are values that we have to consider about and how we differentiate between good and bad. Effort well-done!

    Posted by Katy on February 1,2010 | 08:51 PM

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    Posted by Michelle on February 1,2010 | 08:51 PM

    Very Interesting! What a great story!!!

    Posted by Shernan on February 1,2010 | 08:51 PM

    PS; Scientists know what extends life but there is controversy in affecting this about life, as longer lives could result in more issues later because of living longer it might not mean better quality....they already know which cells in those cause people to live longer...it's an elongated X. They know how to affect this in people, not sure how they do it but it's not in the public market. I know this by working at a biotech company involving DNA and was told by a top scientist during a class.

    Posted by juliehearn on February 1,2010 | 08:51 PM

    WHAT I DO NOT LIKE TO SEE IS THE IGNORANT COMMENTSD THAT ARE MADE ABOUT HER BEING A VAMPIRE! These type of cells as well as cancer,HPV, cells are needed for research. so keep your negative comments to yourself. Think about it, what if your family was stricken w/ a disease? Would you want someone to make her better with drugs that were scientifically proven? or just look at her and turn up there nose and keep going?

    Posted by Hollywood.Gurl on February 1,2010 | 08:51 PM

    My question is whether or not the author is giving a portion of the money she makes on this book tothe family. Its not just big bad medicine that makes money off people, authors like to do it as well. Personally, I think a lawyer needs to reach out to these people to make a finacial deal for them that gives the family either money or a lifetime insurance plan (or both) in exchange for further study of their line if it is that important to them and assures them a percentage of the proceeds from the book sale since the book is about their family.

    Posted by Kelly on February 1,2010 | 08:51 PM

    Wow.........would make a great movie.

    Posted by Frank on February 1,2010 | 08:51 PM

    Shame on all that would make this a racial issue! Shame on those who also are bent on monetary gain. Think of the value of the research, and the honor now being afforded this woman, and her contribution to scientific research. Most of us have given blood and urine for testing. We receive the benefit of what the tests reveal. All of us are giving up cells everyday as we shed them from our bodies. They are usually dead cells. Some are cells we would be better off not giving to someone else because they may be infectious. Who gets paid for becoming infected with disease we might spread? Do you suppose it would be wise to start suing your neighbors because their child infected your child who infected you, and you infected your coworkers? Now you might understand the folly of such ideas of monetary gain.

    Posted by Steve on February 1,2010 | 08:51 PM

    HAT'S OFF, ELEQUENT, MASTERPICE. I'M ALSO A RECIPIANT OF THE POLIO VAC. QUESTIONS, ALL THOSE THAT PROFITTED BY THIS CELL. MEDICATIONS, ETC. THIS IS TO ME AS MR. THOMAS EDISON. THIS IS BIG, SHOULD BE A MOVIE? AL MEN AND WOMEN ARE CREATED EQUAL. BUT ONE CELL MADE A DIFFRENCE IN BLACK, WHITE, LATINO, GREEK ETC. MADE A DIFFRENT IN ALL OUR LIFE. THE DOC AT THE TIME OF THE TAKEN OF THE CELL THAUGHT IT WAS ABNORMAL, TOOK IT WITHOUT CONSENT AND SEND IT TO THE LAB. NOW IT WAS FOUND THAT THIS IS A FOREVER CELL,
    THE FAMILY SHOULD BE CONPENSATED FOR THIS. THANKS MRS LACKS.

    Posted by Rolando Beckford on February 1,2010 | 08:51 PM

    It's a great discovery of all times. I think this will change something in the world of discovery. I believe that deep explanation requires for those persons who did not understand the important of this scientific project. Open-mindedness is necessary for everyone especially to media to support this project that we all know that can save many lives especially children of our future who are most affected of diseases.

    To the family of Henrietta Lacks, I believe its your rights to have what your family really owned. I believe also that whatever your mother left will help your present condition of life in terms of financial problem but I do believe also that she does not want you to be greedy.

    Please try to understand how big your mother can contribute to human life, it will be your honor and self-respect that no amount can valued. Think of it as respect and honor also to your mother's name that forever be there even she is not here in our world physically.

    Posted by MICHAEL MURILLO on February 1,2010 | 08:51 PM

    Great and fastinating story, The family should be compensated

    Posted by Peg on February 1,2010 | 08:51 PM

    wow this is so amazing..ive never heard about hela cells before until this article..it really grabed my attention..were can i purchase this book

    Posted by vanessa on February 1,2010 | 08:52 PM

    Someone posted the comment that her Mrs. Lack's cells are not 'immortal'...they just outlived her. NOT TRUE. Mrs. Lack's cells produce an enzyme upon cell division and this is what makes her cells unique. AMAZING!!! This makes me think about returning to college and studying Biology.

    Posted by P L Newkirk on February 1,2010 | 08:52 PM

    Very interesting story. I too want to read the book. Great job reseaching and bringing this story to so many people.

    Posted by D.Thomas on February 1,2010 | 08:52 PM

    the articles is really great and so much intruiging... i want to read all about the story of "HeLa" on how the government rise the compensation for Henrietta family.... i got interest to the story and wanted to learn more.....

    Posted by pamela reyes of Philippines on February 1,2010 | 08:52 PM

    Very interesting. What I find appalling is people are talking about greed. This isn't about greed; it's about a woman who probably didn't give consent and her tissues were used and made millions for researchers and helped cure people. What we now know is they did some shady things back then and this family, law or now law, should be compensated.
    If it were not for her, these breakthroughs may have not happened or happened alot later that what they did. Granted, when you sign for surgery, you don't own the disguarded matrerial, but it would be nice to know that it is being used. Too much has been done under the guise of "science" and "to the betterment of science" that some of us will buy this bull lock, stock and barrel and not think about how people are priced out of health care and badly needed cures. We need to be careful; just because it is given away doesn't mean you shouldn't be acknowledged for it, or at least mentioned in the scientific annals of science. How many others have been done like this? One person may donate and another may not, but you STILL have to show some type of RESPECT to the person who's cells they obtained through donation or trickeration.

    Posted by Deb on February 1,2010 | 08:52 PM

    a very interesting story... i would loved to if they could make a movie version...well since from the start that the HeLa cell/s were just subjected for experimentation, (hence, we know what scientists' job is and we have to be thankful for such and such of their invention in terms of health treatment), no one ever knows that this will happen up to this point of shocking humanities...
    It was mention that this so called 'immortal cells helped to launched a multi-billion dollar cells, i guess they should consider the Lacks family...given their situation.
    Good story,...Godbless you!

    Posted by mark on February 1,2010 | 08:52 PM

    I love the story. Hopefully it will change the way people think.I hate racism.We are all equal.We all bleed red blood.I think she should have a part in Black History month.It is because of her the we all survive. I am truly moved by the story and will definatly buy the book to read further.

    Posted by shannon on February 1,2010 | 08:53 PM

    This is a fascinating story that could shoot a hole through "racist theory" of inferiority. The current debate about "Stem Cell" research can be given a boost from the finsings of this case. Knowing how insignificant cells are to most people and that are relatively nondescript to laymen, her story can open up new avenues of research into the discovery of cures for such diseases as cancer, diabetes, MS, etc. We must get beyond our ignorance of science and delve deeply into the world of responsible medicine and physiology to uncover these hidden gems of discovery.

    Posted by David Myers on February 1,2010 | 08:53 PM

    wish they can make this a movie...a very intersting story.

    Posted by kiko on February 1,2010 | 08:53 PM

    why is everyone thanking her the scientists are the true heros

    Posted by joel on February 1,2010 | 08:53 PM

    I couldn't tear myself away from this tidbit and snapshot- AND ALTHOUGH ITS JUST A PEEK INTO THE BOOK WRITTEN BY MISS SKLOOT, IT IS VERY INFORMATIVE & REMARKABLE. I SEE QUITE A FEW RESPONSES REGARDING THE LACK OF FINANCIAL COMPENSATION DUE TO THIS FAMILY AS WELL AS MAKING IT INTO A BLACK VS WHITE ISSUE- HOWEVER WE SHOULD TRY TO KEEP IN MIND THAT AT THE TIME THIS OCCURRED, THE WORLD WAS NOT IN A MONETARY MINDSET BUT A SCIENTIFIC ONE. I AM MOST POSITIVE THAT THE PERSONS RESPON FOR SECRETLY REMOVING THE TISSUE SAMPLES "DID NOT" DO IT FOR MONEY BUT MORE SO IN THE NAME OF SCIENCE-WE ALL KNOW THAT IF THE ANONYMOUS-IDENTITY MASKED-DONOR HE-LA COULD BE RESEARCHED AND TRACED AND LOCATED THEN WE COULD JUST AS EASILY FIND THE MYSTERIOUS ONE WHO MADE THAT SECRET COURAGEOUS STEP AND ALSO TRACE WHO THIS PERSON WAS AND HOW MUCH MONEY THEY ALLEGEDLY GAINED, IF ANY AT ALL. IT IS WHAT IT IS AND WHAT SHOULD BE MORE INVALUABLE IS THE AMOUNT OF KNOWLEDGE, GROWTH AND ACHIEVEMENTS OUR WORLD HAS THANKS TO THIS WOMAN WHO NEVER KNEW SHE WOULD EVEN HAVE SUCH AN IMPACT TO SO MANY FOR SO MUCH! THAT IN ITSELF WILL FOREVER CONTINUE TO UPSTAGE ANY DOLLAR FIGURE WE BELIEVE IS DUE OR HAS BEEN GAINED FROM THIS ALL. WHAT SHE HAS CONTRIBUTED TO OUR SCIENCE IS P R I C E L E S S !! LETS KEEP OUR FOCUS ON THIS POSITIVE AND NOT THE NEGATIVES PEOPLE.

    Posted by NECHELLE NETT on February 1,2010 | 08:54 PM

    WOW. I loved this story. Thank you for writing it.

    Posted by Sandi NYC on February 1,2010 | 08:54 PM

    That is very amazing story makes me wonder how this is possible maybe other people have different type of HeLa cell, the cells probably regenerate them self it was a part of there DNA another form of evolution.

    Posted by Marvin on February 1,2010 | 08:54 PM

    i think that it's cool that her cells are still living and it's kinda freeeeeeeeeeeeeeeeaky!!!!!!!!

    Posted by maddy on February 1,2010 | 08:54 PM

    Posted by James Jones on February 1,2010 | 02:00PM

    "Ironically white Americans were unaware that a Black womans DNA was being used in vaccinations that Im sure the majority of Americans received. I think that's the reason for the secrecy. People would have rather died of Polio than received a drop of black cells injected into their bodies."

    Wow, you really need to take a course in how vaccines are produced. Nobody had her cells injected into them. I'm so sick of everyone whining race all the time. Grow up, and before you make any other inflammatory comments make sure you have your facts straight.

    Posted by Kim on February 1,2010 | 08:55 PM

    Wow Paperz. Really? The cells were taken from a biopsy sample that was extracted from her cervix to be tested for cervical cancer. I suppose they should have had her sign a release form and have paid her a dollar for the bit of tissue they excised in trying to save her life. Believe it or not, not everyone was focused on race back then or now.

    Posted by krazychemist78 on February 1,2010 | 08:55 PM

    question, was it discovered later in life they were still alive in that case they didn't know the value of them until later scientists had arrived to realizations, what did they find then vs now about these cells. What were the DNA/scientific differences did she have more helix info?

    Posted by juliehearn on February 1,2010 | 08:55 PM

    I find this whole story very interesting, but I am here to tell you that this story in not unique. Researcher Scientists have been doing research and experiments on many Americans from many different races for years. Most of our medical breakthroughs have had study group participants and some who did not know they participated. Our military men have been guinea pigs for many experimets through the years. I have personally done Research studies and have taken new pharmaceutical drugs.

    Posted by James Bryant on February 1,2010 | 08:55 PM

    I am from the Philippines. A sign on a door in a corridor of laboratories in our institute reads, 'HeLa cells.' Henrietta Lack's contribution to science is indeed immense and worldwide. Research ethics has come a long way; and just like science advancement, when something is realized or becomes known and understood, we adjust, think things over, and do what is right.

    Posted by Fe on February 1,2010 | 08:55 PM

    What a great story. We cannot hold the doctors and researchers of the 1950's to the standards of today. Thank god they kept some of the cells and research was done and lives saved. It is a shame that a young lady died of cancer, but she will now be immortalized by this book. I think the racial comments are absurd , backwards and mindless. I guess if we get really absurd we could say that her cells produced the polio vaccine that Bill Gates took as a child and he might not have survived without it , so he owes someone part of the money he made because of the vaccine he took. People are poor because most of them make bad decisions or have bad habits. It is not because of skin color , or medical chicanery. America needs to celebrate this great accomplishment and woman , not try to extract money from it. If there was a conspiracy it was not very successful as the book was after all written and the truth is out. The researchers could have easily lied about the doner's identity and made her who ever they wished if they had a racist agenda.

    Posted by Alan Tooran on February 1,2010 | 08:55 PM

    the first time i comment here. a great job, fascinating and thought aspiring. it should be awarded a Ph.D degree. but regarding the family, they should be compensated. some thing seems wrong to me...

    Posted by from KURDISTAN on February 1,2010 | 08:56 PM

    Why is everyone wondering if she was compensated. It just seems to me that her contribution and immortality for being involved in this research is more than adequate!

    Posted by John on February 1,2010 | 08:56 PM

    mrs.Lacks is dead,long live her cells and her legacy.

    Posted by chris on February 1,2010 | 08:56 PM

    As I read some of the comments about this article, one thing that I see MOST people missed was that if this women cell can live and be a part of so many NEW developments of today regardless of any persons views, it simply states that the answer to ALL our HEALTH issues are within ourselves, and we ALL need the that mrs. Henrietta Lacks. If you look hard enough it is tell you something, WE are the begining and the end.

    Posted by D. ford on February 1,2010 | 08:56 PM

    Wat a story, Yes a movie should be made.my parents died one month of each other in the early 60s.I would say that their passing was not in vain if it helped save lives..

    Posted by lucia on February 1,2010 | 08:56 PM

    Unfortunately, unless you've ever lived in poverty and been in the same cirumstances; of using someone or their cells, and being the first to accomplish so much,I can see the family being angry. I like your piece. I now walk away with a new understanding of HeLa cells. Thank you.

    Posted by MISTY MEDINA on February 1,2010 | 08:56 PM

    Does that mean people with the polio vaccines have her cells (Henrietta's) on them? What can the racists have to say now if they, too, have had the polio vaccine? Kudos to Henrietta and her family.

    Posted by Glenn D. Torres on February 1,2010 | 08:58 PM

    Why does it always have to be about how much money somebody can get out of it?

    Posted by Toni Vercillo on February 1,2010 | 08:58 PM

    Wow! This is a really amazing story. As I saw this, I was like, this is just too much to read. But then I began to read and I got really fascinated with this story. This REALLY makes me want to buy the book. Oh yeah, if I was part of the main part of Henrietta's family, I would sue those scientist for every little penny they have. Other than that, THUMBS UP STORY!!!!!!!!!! (Especially for a 13 year old.) Yep, that's right I'm 13 years old. :)

    Posted by Shantoria Pollard on February 1,2010 | 08:58 PM

    Interesting. I'll be looking for the book. It was sad to read about where her son is now.

    Posted by gloria on February 1,2010 | 08:58 PM

    I don't think there was a cover-up, I don't think there was a malicious "stealing" of her cells. In 1951, the doctors simply took a sample of strange cells to be studied and, in this case, replicated. It was their work on these cells that resulted in the advancement of medicine not the cells themselves. Henrietta Lacks was an unfortunate woman who died a terrible death, but at least something good came of it. Does the family need to be compensated? We can't look at this in the context of medical research today, where every legality is checked into and covered. It would be nice some memorial fund were given to the family but they don't need to be handed over the large amounts of money that was generated from other people's hard work.

    Posted by Les on February 1,2010 | 08:59 PM

    Wow! you got me hooked up with this, very nice and very interesting!

    Posted by Irish on February 1,2010 | 08:59 PM

    This is awesome I love learning new things but what did Mrs. Lack die from in the end?

    Posted by Izabia on February 1,2010 | 08:59 PM

    Amazing story. To answer the 'what happened then?' question, read the book. By the way, collecting tissue samples without explicit permission or even knowledge from the patient or the patient's family was common practice in the 1950's. Even for some time after that. No laws or standards were broken at the time. Henrietta did not suffer as a result of the tissue sample, either. I'm not saying it's right or wrong, just that the doc was neither malicious nor did he violate the principles of the time. The cells were not "stolen" from anyone. They were from a cancerous tumor. People donate their tissues to science all the time with no compensation needed or asked for. Millions a day.

    Posted by Mark on February 1,2010 | 08:59 PM

    All you money mongers out there, everytime a woman gets a PAP smear, there are tissue cells collected. Same with guys and gals having biopsies etc.

    Posted by Toni Vercillo on February 1,2010 | 08:59 PM

    I've got interested to read the whole story.

    Posted by Nico on February 1,2010 | 08:59 PM

    This is really mind blowing. I'm 17 years old and I'm really into medicine and this story is out of this world. God Bless her!!!!

    Posted by shah on February 1,2010 | 09:00 PM

    Thanks for sharing. I don't read much but when I do it takes me to another level of understandind the world. This was great news! I hope the family got some type of compensation from all this. They should benefit as science has. They should not be millionaires but should live comfortable lives. I like to know why her cells did not die when other cells didn't last long enough to be tested. I am not into science nor have any degree but an associates in computer programing. I just like to learn about changes that affect all of us. Thanks for your story. We all have one that changes our way of thinking in some way or another. Thanks!

    Posted by Julio Meneses on February 1,2010 | 09:00 PM

    Henrietta's tissue was collected to see if she had cancer and she did. Had she been alive today she might have found a cure.

    Posted by Toni Vercillo on February 1,2010 | 09:01 PM

    Wow, what a way to get someones attention. The way you have with your words just draws me into the story even more. I am not much of a reader, but tomorrow I'm gonna treat myself to a new book. I am very excited to read this particular book. You speak so highly of Henrietta Lacks. She seems to have been one "Hell of a Woman!" I hope the lifetime of questions Deborah had were answered in extreme detail. It is sad that the doctor did what he wanted to and not include her in his decision, but then again we would not be having these conversations based on Mrs. Lacks if the doc did not do what he had. God works in Mysterious ways!

    Posted by Brandy Thompson on February 1,2010 | 09:01 PM

    I'm not surprised. This is only one account of how people are used as specimen in labs that date by many years. Look up the Tuskegee experiments.

    Posted by Jen on February 1,2010 | 09:01 PM

    very interesting!

    Posted by marizz on February 1,2010 | 09:01 PM

    Thank you for the interesting article. However, the story is not new. I think that Ebony Magazine contained an article on Mrs. Lacks. The article was written in the 1960's. Perhaps the aurthor or Smithsonian could confirm this?

    Posted by EbonyReader on February 1,2010 | 09:01 PM

    this story rocks. i hope a documentary is made out of it some day, soon preferably. thanks Miss or mrs Sarah Zielinski.

    Posted by donald elong bakong on February 1,2010 | 09:02 PM

    The case of Moore vs Regents states a patient is denied rights to their own tissue. Please read a summary of the case via this link http://www.newscientist.com/article/mg12717260.100

    However, some there should be some sort of public acknowlegdement of how much the HeLa cells have contributed to medical research and development. It would be great PR for a major biotech corporation to honor the Lack family and donate some type of award.

    Also, I hope some proceeds of the sale of the books will go to Mrs. Lacks surviving family as some sort of compensation.

    Posted by Annie T. on February 1,2010 | 09:02 PM

    What an interesting article. When is humanity going to realize that civilization, along with HeLa, derives from the soil of black women. No, this is not a racial statement, but it also goes to show you how the white race has stolen something once again without compensating those who help fill their greedy little pockets.

    I think it is a wonderful thing that her cells have helped to accomplish so much in medicine. I can't wait to read the book. I hope her family gets back compensation out the wahzoo!!!

    Thanx for book release Vanessa!

    Posted by Mimah on February 1,2010 | 09:02 PM

    Let me know when the movie is being shot. I would love to be an extra!

    Posted by E Stacy on February 1,2010 | 09:02 PM

    Wonderful story. This would make a great movie. NOT staring Halle Berry.

    Posted by Margaret on February 1,2010 | 09:02 PM

    We're talking 1950's, this was new, cutting-edge science that all of humanity has benefited. Nobody was trying to cheat anybody out of anything. They did'nt even know what they had, or what to do with it.

    Posted by Toni Vercillo on February 1,2010 | 09:02 PM

    All of this talk about money and rights to parts of your body has completely obliterated the true meaning of this story. Behind all of the jiberish lies the fact that this procedure(s)has been a key factor in the human race surviving and flourishing! There is no race,wealth, or laws written by man that can begin to acknowledge the fact that what happened with her cells may be the very reason we are all still here and alive. Throughout history, many stories have been told about great discoveries changing the future, and often overlooked is the fact that without these things happening, there may not, or have even been a future! The real point of this being public knowledge now should only be to let each and every one of us know that no matter what we do or say, however small or large a part we take, everyone has the ability to help the human race survive, and progress through constant new diseases, or old ones that have mutated (H1N1), often times(as in Henrietta Lacks case)without ever knowing the impact it has made. There is a much bigger picture we all often overlook that directly affects generations to come. Please notice what I'm saying has absolutely nothing to do with scientific morals, pharma greed, military power, political, or even personal gain. God Bless all who have contributed knowingly or not, and now let you be recognized for being part of the reason we are all still alive on Earth.
    marc_65@live.com

    Posted by Marc on February 1,2010 | 09:02 PM

    is thia for real? wow!

    Posted by filipina on February 1,2010 | 09:03 PM

    The doctor who removed the cancer from Henrietta Lacks while trying to save her life definitely should have paid her a lot of money, at the very least a million dollars. He should have known that 50 years later her cancer cells would be worth billions and billions.

    In fact, everyone who has a cancer or a body part removed during medical treatment should get a minimum of $1,000,000.00 just in case 50 years from now the evil (and potentially racist) scientists develop something useful from the removed tissues. That'll teach those greedy doctors a lesson or two!

    Also, this has the wonderful side effect of solving the health care insurance problem. Everybody just has to have surgery and they come out of the operating room as millionaires. Problem solved! We need to get President Obama to back this idea if he doesn't get his health care bill passed through Congress.

    And after that, we just need to get President Obama to raise the minimum wage to $1000/hour so that we can all be rich!

    Posted by Guillermo on February 1,2010 | 09:03 PM

    Very interesting. That shows how we will be resurrected on the day of judgement.

    Posted by Mohammad A Rajpoot on February 1,2010 | 09:03 PM

    Lol. Why are some people demonizing the doctors? So if you had a meningioma and had it taken out, you would rather have it thrown away than used for science while you remain uncompensated? (selfish much?) Also, scientists aren't millionaires. I attend one of the best research universities in America. They are brilliant and kind and usually not wealthy. The Pharm. companies make the profit. And no, keeping her identity was not about her being black. They simply knew that some people would declare discrimination and demand compensation. And to answer your questions..they are still living because that is the definintion of cancer cells. They lack regulation of cell cycle due to un-regulated Cyclin Dependent Kinases or inactive Tumor Supressor Proteins, or a host of other things we don't understand. Thank God for this woman's contribution and the scientists ingenuity. Some of you would refuse to cure cancer because you'd rather have cable television.

    Posted by Cswilkins on February 1,2010 | 09:03 PM

    It's amazing how the scientific community recieves millions in research grants and free tissue samples from the government (read taxpayers) yet when the miraculous breakthrough comes, It's some big drug company that reaps the rewards and we get a new $120. miracle pill.

    Posted by David Baganha on February 1,2010 | 09:04 PM

    Incredible Story!

    Posted by Daphne Johnson on February 1,2010 | 09:04 PM

    Wow! What a great way to open up Black History Month!

    Posted by http://www.allkidseatfree.com on February 1,2010 | 09:04 PM

    this is amazing! i am 15 years old, and now i wish we could learn about this type of stuff in my biology class! very good piece, good to the last word.

    Posted by bre marie on February 1,2010 | 09:04 PM

    I suppose we will have to buy the book to find out THE REST OF THE STORY. Which brings us back to the whole making money off something. Let's ask the author if she plans on donating part of her proceeds of the book back to Henrietta's family.

    Posted by Toni Vercillo on February 1,2010 | 09:04 PM

    Rececca Skoot has set up the Henrietta Lacks Foundation, which will use some of the book's proceeds to provide scholarships for minority women scientists. Special preference will be given to young women from the Lacks family.

    http://rebeccaskloot.com/book-special-features/henrietta-lacks-foundation/

    email me if you want to learn more. antonyio_2000@yahoo.com

    Posted by Edgar Garner on February 1,2010 | 09:05 PM

    I find this article awesome. Thank you.

    Posted by Houari NY on February 1,2010 | 09:05 PM

    I'm an award winning psychoanalyst who taught the New Guinea aboriginals to be able to point at each other in the late 1950's. In my professional opinion, whatever their other merits,the couple in this photo appear to be cracking up.

    Posted by Rod Meehan on February 1,2010 | 09:05 PM

    Wow! this was nice.

    Posted by dhutchi on February 1,2010 | 09:05 PM

    This story is one in a million untold stories when speaking of how much has been stolen or taken from black folks. This particular story further outlines why reparations are in order to millions of black people. Sooner or later, most of us will realize that the wealth of the wicked is already stored up for the righteous. Everything that goes around, will come back because it is the natural order of the Supreme Being. All you wicked people, and you know who you are, your turn is coming.

    Posted by Barbara Simms on February 1,2010 | 09:05 PM

    Wonderful article and interesting story!! Would love to read the entire book.

    Posted by Meera on February 1,2010 | 09:05 PM

    What a story. This however is just a spec of sand on any given beach which depicts the many ways in which the "suttle pains grow into large problems. It is so sad that many in our society see so many of us "vulnerable." I enjoyed what I read and thank you for giving me a brief history on what I know will soon be many.

    Posted by E. Cleveland on February 1,2010 | 09:06 PM

    I find it disgusting that the family wants money for doing literally nothing. I would be extremely proud if someone told me cells from my dead parent have saved the lives of countless others, cured diseases and furthered our understanding of nature. Instead this family only cares about financial gain. Gross. That's almost like charging people for your dead mothers body parts.

    Posted by John on February 1,2010 | 09:06 PM

    Before my father died of blood cancer, tissue samples were taken and sent to laboratories. He's physically gone but his contribution in the medical field through these "tissues" is helping the medical students/researchers understand the disease process, and hopefully save more lives.

    Posted by amelia on February 1,2010 | 09:06 PM

    Paperz:

    Nice conspiracy theory. Then why did they keep it secret up until the mid-70's if it was about race? It wasn't. Im guessing you see race in everything. It was about money though, which is nearly as bad.

    Posted by on February 1,2010 | 09:07 PM

    If money is to be given this ladies family it should be from the book sales. If the family doesn't receive compensation from the book, then they should seek legal remedies.

    The ladies color is not the important part of this story. How stupid do you people think we are? Do you actually think we care about her color. This is a human interest story. Human = all colors.

    Why do we have "Black" History month and not "yellow/white or pink"? Why not "American" History month? Let's stop perpetuating race differences.

    Truthfully, when I saw the picture I didn't think of them as black. And I didn't read the story because of the injustices of the 1950's.

    The people of America need to remember we are one race. The human race. We are one country, America.

    Mrs.Lacks made and is making an incredible contribution to science. She looks like a beautiful woman and I'm fairly certain she was a great wife and mother. I hope her family can accept the fact that she was an important piece of science discovery without feeling a need for compensation.

    I really want to read the book.

    Posted by Hank on February 1,2010 | 09:07 PM

    wow! it's amazing, althought i'm not a scientist i can understand a bit of it and it's great reading and informative since it was done 25 years ago...hope that her family will get compensated.

    Posted by Ed Castro on February 1,2010 | 09:07 PM

    I am truly amazed at the fact we're not taught important information like this in school. Incredible story, thank you to the author and Lacks family for sharing.

    Posted by Nisha on February 1,2010 | 09:07 PM

    Kudos to the curious,diligent and brilliant mind of the author. May his blessed name be as "immortal" as the HeLa cells themselves.
    The life and peace which the world's great powers could not furnish to humanity, despite their material granduers and pomps, the Nature has bestowed through the cells of a dead, abject "black" woman. How many souls have been saved? How many job opportunities created? How many billions of dollars have been made? How many great names have been born? Yet, all consequent upon the "cells" of a poor, helpless dead soul.
    Ultimately, it all goes to assert and prove the Self-subsistence of the Supreme, Living and Eternal Creator of matter and soul. And ultimately, the HeLa cells shall perish along with every other soul and matter. But, their Sole Originator shall live and never, ever die!

    Posted by Azeez on February 1,2010 | 09:07 PM

    That's a great story, I would love to read the book, where can i purchase it at i hope the family get something from this, money and lots of it, because that is from a very long time ago

    Posted by brenda on February 1,2010 | 09:08 PM

    Interesting. I really loved this article. I am going to buy the book. I REALLY LIKE the question raised by a poster, that it was the diseased cells that have not died yet? Science of any sort really spreads my toes.

    Posted by Sean Snowden on February 1,2010 | 09:08 PM

    I knew God was amazing, but WOW!! You are awesome ELOHIM--Creator

    Posted by Vernice on February 1,2010 | 09:08 PM

    Just another example of the exploitation of Afican Americans against their will and without their knowledge.Where is the bio-ethics in this?

    Posted by Julia Boswick on February 1,2010 | 09:08 PM

    No one should be taken advantage of regardles of color creed or just plain living and religeon. We all are equal so we should be told and let the people decide. Our body parts shoul never be up for sale, if we would like to donate our body it should be a gift to metical sience and help other people get well.

    Posted by F. Fallon on February 1,2010 | 09:08 PM

    On the comment of sir william thomas I just dont know if what is in his mind. the way i understand this significant issue surfaced only because of the untiring invistigation of madam rebecca skloot. without her we do not know that the polio vaccine we recieved came from henrieta lack, without her the family of henrieta had no knowlege that out of the cell of their mother, wife or sister somebody earned billion, it was that investigative report that the world know of that immortal cell....

    Posted by orlando m. bautista on February 1,2010 | 09:08 PM

    Final Analysis:
    1) Yes it is agreed that the cells were used for research
    2) Yes it is agreed that these cells were discovered to be (apparently) one of a kind cells
    3) Yes it is agreed (but not substantiated) that the reason for the secrecy around the donor was because they were from a black person. (Personally, I feel that at that time just being from a woman would have been bad enough)
    4)Yes it is agreed that these unique cells were used in the production of many vacinations
    5) Yes it is agreed that these cells made manufacturers of these vaccinations millions upon billions of dollars
    6) Yes it is agreed that samples are extracted from millions of people each year
    7) yes it is agreed that you, me, my parents, my children, and my grand children all owe a great debt of gratitude to the FREE POILIO Vaccination shot we received
    8)No it is not agreed that the millions of people in this country think that all the scientists and drug company investors in research for the benifit of mankind owe this womans family a dime.

    Solution--everyone in the country (including the scientists and investors) donate $1 to a fund set up by her kids to show the country's gratitude for her uniqueness,and memory should amount to any compensation anyone commenting on this article's subject could and should expect. Add the donation web-site in the back of the book and I'll be happy to give my dollar.

    8) I hear they found a gene for vacinating aids. I lost a couple people to that one so let's keep this going and hooray for the scientists and big investors that are in it for our well being...plus a buck lol

    Posted by skibotex on February 1,2010 | 09:08 PM

    I'm really excited to read the book. You can not help to think whether something like this has happened in your own family, and remains a mystery. How unsettleing. The author has done an amazing investigative work. How he arrived at the truth about Mrs. Lack has to be a story in and of itself.

    Posted by pg legg on February 1,2010 | 09:08 PM

    Hmmmm... One person writes a book and hundreds more are willing to accept it as fact and spend their money to buy it. Who did the research and who has verified anything written in the book?

    And it's really ironic that so many people ask if the family made any $$$ from the situation if it did happen.

    This article is nothing more than a plug for a book.

    Posted by Reverend Dewey Cox on February 1,2010 | 09:08 PM

    i dont even read that much of this genre of a book, but wow this is incredible! good luck with the book and definately should be a good read!

    Posted by stela on February 1,2010 | 09:08 PM

    Money! Compensation? For what?
    I it is illegal to sell body parts.
    Hospitals routinely take tissue for testing and research.
    It is a wonderful, interesting story that should be told.
    But nothing is owed to anyone and racism has nothing to do with it.

    Posted by Charles Foster on February 1,2010 | 09:09 PM

    Amazing story and hopefully a lesson for us all. We must move ahead into an open, inclusive society or this great experiment of human evolution will fail.

    Posted by newsbyyou on February 1,2010 | 09:09 PM

    Great article. This is how doctors stole your organs. Especially poor people. This is an example of human piracy.

    Posted by RogS on February 1,2010 | 09:09 PM

    The article was very interesting and shows how analyzing human cells, in this case, cells belonging to a woman who had cervical cancer, can lead to medical strides in research and treatment of diseases, etc. I don't believe attaining Mrs. Lacks cells was a money-making ploy of any sort, as has been suggested by some others who made comments. On the contrary, these cells were used to help others. I would imagine Mrs. Lacks would of liked knowing that she has been able to help others with her "immortal" cells, which were fortunately able to thrive throughout the years. It is a shame that her family was not financially well off, but that does not give them the right to be greedy and gain from their mothers ability to benefit others from the grave. Also, others who have commented and tried to make this story into a racial thing are wrong...she may of given of her cells unknowingly and by not the most ethical way, but it is not common knowledge that African-Americans were the ones behind the medical knowledge needed to use the cells to benefit others through medical research and treatment. Those contributions may have come from other educated African-Americans at a later date, but who really contributed during Mrs. Lacks time? Mrs. Lacks story is one of many which has benefited mankind and that is to be commended. But why do some commenters have to make it a 'black' thing and only give credit to a black woman and not recognize the many scientists, white and black, who have worked behind the scenes in laboratories across the world over the years, who are trying to help ALL humanity through cell tissue research?

    Posted by Tim on February 1,2010 | 09:09 PM

    Great Story. There are so many great things African Americans have done that they has not been recognized for. I would buy the book. I hope the family will be compensated. This is very interesting and I hope it will helpful for the daughter. The cells has been good for and positive contribute to science.

    Posted by Vickie Parker on February 1,2010 | 09:10 PM

    Pay the next of kin, STOP! using people without premission,that's COLD...

    Posted by rita on February 1,2010 | 09:10 PM

    I am a cancer researcher in the United States. The review seems solid, but may be misleading in one regard. The statement,

    "The people behind those samples often have their own thoughts and feelings about what should happen to their tissues, but they’re usually left out of the equation."

    is only half true. Changes in the ways patients are involved in research have changed drastically in the last 50 years, and in my experience, researchers are very good now about obtaining patient consent under the auspices of an institutional review board. All clinical specimens are required now to come from informed individuals who have given their consent. In short, what happened to Henrietta Lacks' cells in 1951 almost certainly would not happen in 2010.

    To answer a couple of comment of interest:

    1) Polio vaccine did not include "black cells." Vaccines are derived from dead *virus*, not dead human cells. HeLa cells may have been used in polio *research*, but this does not equate to their incorporation in the final therapeutic agent.

    2) While I do not agree with the way the tumor tissue from Henrietta Lacks was handled, one should keep in mind that --
    a) any money doled out to the provider of specimens is less money that can be used on research, which means less information to the researchers and less benefit to humanity

    b) it was *tumor* tissue. What would Henrietta Lacks' family have done with it?

    c) the removal of the tumor was in her best interests at the time and its' removal would not have harmed her.

    Mrs. Lacks should have been informed about the potential use of her specimen before obtaining her consent. No more effort was necessary, and it would seem that her family's clamoring after money had no positive effect on the research community, as informed consent became a part of the research culture without their lawsuits.

    Posted by A1 on February 1,2010 | 09:10 PM

    Were some of the cells used to conduct cervical cancer research?

    Posted by Elna on February 1,2010 | 09:10 PM

    We ARE all related .

    Posted by Breunna on February 1,2010 | 09:10 PM

    what an incredible story!

    Posted by alex on February 1,2010 | 09:10 PM

    The world owes a debt of gratitude to Henrietta Lack and her family is likely owed billions of dollars but who is going to pay them? I hope they were given something in return for the 'gift' their family member unknowingly bestowed to medical and scientific research but I wouldn't hold my breath on that. Also, I can't understand why some people see this as some sort of 'inspiring' story which should be held up as proof that 'African Americans' have value and have contributed greatly to America and the world. Of course they have made invaluable contributions which have neither been appreciated nor acknowledged (in many cases). Ms. Lack was taken advantage of simply because she was black and poor. This was not inspirational, it was greedy, evil and indicative of just how corrupt, racist, prejudiced, arrogant and criminal many areas of American society were (and still are in some cases). African American and other racial minority groups as well as the poor, uneducated, and disadvantaged have been experimented on against their will (and knowledge and most cases) for centuries. Marion Sims, the so-called father of modern gynecology, experimented on pregnant black slave women using pointed shoemaker awls during the late 1800s. Most of the women died of infections due to his 'experiments'.

    Posted by ShinetheLight on February 1,2010 | 09:10 PM

    What this article lacks is "how common are immortal cells?" "who has them and why?" and most importantly, "does having natural immortal cells mean anything to the individual other than, 'i have good cells for science"

    Posted by Dawkins on February 1,2010 | 09:11 PM

    I wholeheartedly agree, this is an amazing article! My grand-daughter and I read it together and she is now interested in science, and says "very interested in science." Due to this article she will start taking science more seriously. Thank you HeLa for your scientific research cells. May God Bless this family.

    Posted by Mama-lisa 58 on February 1,2010 | 09:11 PM

    In 1913, poor children in a youth home were deliberately infected by their doctors with tuberculin and allowed to go blind as a result. Their experimenters/torturers were never punished. In 1915 under the direction of the US Public Health Office, Dr. J. Goldberger infected black prison inmates with a central nervous system disease in an attempt to find a cure. The cause of the disease was known already (niacin deficiency) but because the inmates were 'only black' they were not given the cure. In the 1930s Rockefeller Instit for Medical Research Pathologist Cornelius Rhoads, deliberately infected many Puerto Rican patients (a number of whom died) with cancer cells. He covered up details of the experiment but this was later found out. Was he remorseful? Hell no. Rhodes gives a written testimony to the effect that all Puerticans should be murdered. Instead of being sent off to a prison psych ward as he should have been, this psychopath goes on to establish the US Army Biological Warfare facility in MD, UT and Panama, and is named to the U.S. Atomic Energy Commission where he continues his sanctioned murders by experimenting on and exposing American soldiers and civilian hospital patients to radiation. One can only imagine what is being done now in the name of science and medicine - I'm sure we as a nation of people are routinely experimented on. With all the vaccines for this and that and man-made diseases one can only imagine and shudder in fear. What we Americans don't realize is that when we sanction the mistreatment and abuse of certain members of our far from democratic society because we think they are 'less valuable', then we in fact sanction the same for all of us. Our nation has been sowing the seeds of our own demise for centuries.

    Posted by ShinetheLight on February 1,2010 | 09:11 PM

    Funny...deserved / undeserved in whatever aspect of "anything" these days involving helping mankind..money is ALWAYS involved.

    Posted by mcorey on February 1,2010 | 09:12 PM

    Very interesting article.

    Posted by Mark Jayson Mojica on February 1,2010 | 09:12 PM

    Very intresting story. I learned a lot

    Posted by Kris on February 1,2010 | 09:13 PM

    Amazing Story! There is always a reason someone becomes so dedicated to telling a story...This was the best story Ive read in a long time.

    Posted by Mary on February 1,2010 | 09:13 PM

    For those that don't understand what "immortal" means: I learned about HeLa cells in microbiology in 1993, and this is what I remember: HeLa cells are CANCER cells from Henrietta. The reason cancer cells are a disease is because they DON'T die out after 90 or so replications, which is what normal cells do. They keep multiplying, which creates tumors in the body. If a single cell "falls off" a tumor, it can plant itself anywhere else in the body and begin another tumor. When many cancer cells do this, it is called "metastasis" and can create ANY number of tumors, ANYWHERE. This is a very dangerous stage of cancer.

    This limitation of normal cells is very limiting for esearchers. A human cell that keeps dividing and never dies is like gold, like platinum for DNA research.

    As for the ethical implications, the cells are BOTH Henrietta and her disease (cancer). I agree that her decendents should receive a portion of the profits from the sale of her cells, even if it incurs a retroactive loss. Isn't it worth the knowledge we have gained?

    Posted by smartyhands on February 1,2010 | 09:13 PM

    I wonder if she was murdered because of this "immortal" DNA of hers. Maybe she was capable of longevity as Adam and Eve were once.

    Posted by Lena on February 1,2010 | 09:13 PM

    Thw HeLa cells are "immortal" meaning they divide indefinitely, not only 40 times like any other human's cells, like ours for instance. Of course the HeLa cells die too, but their descendants live on and divide in their turn. Regular cells stop dividing after 40 times, and eventually die.

    Posted by Honorius on February 1,2010 | 09:13 PM

    Very interesting story. Talk about good genes, could there be more steming from the cloning and the In vitro fertilization.

    Posted by H. Long on February 1,2010 | 09:14 PM

    Great story! The best part is your heart and sensitivity that comes through. I'm proud that you wrote as you did. It's not about money or whatever - it's all about people and being sensitive to them as human beings as we all share this planet together. Somehow, I believe God used this lady for her contribution to all of humanity. She probably knows that now and is smiling. I like to think that is so.
    Blessings on you - Janet

    Posted by Janet on February 1,2010 | 09:14 PM

    very nice piece!!!!!

    Posted by brand-o on February 1,2010 | 09:14 PM

    the intention for the advancement of medical research is good because it is for the benefit of mankind. years had passed, laws were created after almost a decade already but IM MORE TOUCHED BY THE SITUATION OF ONE OF HER SONS WHO WAS MENTIONED BEING HOMELESS AND LIVING IN THE STREETS IN BALTIMORE.IM CONVINCED THE IMMEDIATE FAMILY SHOULD BE GIVEN RECOGNITION IN BEHALF OF HENRIETTA AND AT THE SAME TIME ARE ALSO ENTITLED I BELIEVE FOR MONETARY BENEFIT CONSIDERING THAT IT WAS ALSO MENTIONED IN THE ARTICLE THAT THIS PAVED THE WAY TO THE LAUNCHING OF MULTI=BILLION DOLLAR TISSUE CULTURE INDUSRY.

    Posted by eimohr on February 1,2010 | 09:15 PM

    Wow! I hope someone does what is right! It would only be right for the family to be compensated for the cells that was taken and brought forward hope for the future!

    Posted by twan on February 1,2010 | 09:15 PM

    cancer cells don't die ;)

    Posted by HikerChik on February 1,2010 | 09:16 PM

    White folks continue to amaze me! My mother attended Kent State University when Blacks could not reside in the dormitories. She taught me that I should be civil and respect everyone regardless of thier lack of humanity to me. Ma, I respect you, and attempt to live up to your values but come on..... There is hatred and a total disrespect for people of color. To some, we will always be something only to experiment with, something less than human. Monetary rewards are not even part of the equation. It has to do with certain parts of the population who still believe that white skin is somehow superior. Black folks are less than human, "let's do some medical research on them that we would never do on our own! Regardless that something positive results from our tinkering. We don't have to give credit to their contributions". God help some folk. Blacks have contributed so much to building this country....Oh well, so many things have definitley changed, but so may things remain the same. Tuskeegee, anyone?

    Posted by Karensb on February 1,2010 | 09:16 PM

    fascinating...thank you 4 doing the research. i do hope the family gets something.

    Posted by shany on February 1,2010 | 09:16 PM

    I am in 7th grade and was fascinated by this article. They do not teach this stuff at school, and I think that that is really a shame.

    Posted by allison on February 1,2010 | 09:17 PM

    It is amazing. I would like to know more about the story.

    Posted by M nguy on February 1,2010 | 09:17 PM

    Sorry to be a naysayer folks. I have taken Biology classes
    in nursing school and never heard of this so-called HeLa
    cell theory. I SUSPECT it to be a hoax, spread like wildfire like Bigfoot, UFO's and get rich schemes.

    Posted by Cynthia on February 1,2010 | 09:17 PM

    Nice story. These are the kinds of stories that need to be told. I am curious, since you stand to make alot of money on the book, are you going to share the profits with the family?

    Posted by Marty on February 1,2010 | 09:17 PM

    I say if someone can benifit even years down the road you can HAVE any cell you want.

    Posted by kvred on February 1,2010 | 09:17 PM

    very interesting! can be made into a movie maybe

    Posted by che lacson on February 1,2010 | 09:17 PM

    Ahhh so that is what those evil caucasian scientist and doctors do without your consent. Shaking my head...I hope this family has a good lawyer. To quote an Ozzy Osborne song "Their Jekyll doesn't hide" in other words, these beasts are telling on themselves now.

    Posted by Ash on February 1,2010 | 09:18 PM

    Amazing...just absolutly amazing...Where can I get the book?!?!?!?

    Posted by Crissi on February 1,2010 | 09:18 PM

    This woman's cells lives on today John's Hopkins and medical facilities the world over are still growing and using them, yet as a member of her family says "we can't even afford healthcare". I found another article which is even better under Johns Hopkins By Ms Skloot where they tested other living members of her family, yet refused to follow up with them about the outcome of the tests. These are simple people so they just seemed to have given up, black people just get taken advantage of over and over. ( this explains so much even today, when Tom Joyner every yr has to do the Take a loved one to the Docter drive ) I have sometimes thought why does it take this much, to get people to see the doctor........but I guess there is a history that is deep seated. I want to read the book but I am not comfortable that now authors/publishing houses are gonna make money off Henrietta Lacks and I still have not heard a word about compensating them.

    Posted by Lee on February 1,2010 | 09:18 PM

    enjoyed this piece very much. well written both from personal and scientific side. thanks for sharing!

    Posted by kathryn on February 1,2010 | 09:18 PM

    So if she was actually immortal then she never really died. So she's alive, basically. That's cool but weird. SHE IS ALIVE!!!!!!!!!!!!!!!!
    She is immortal!!!!!!!!!

    But if she was dead then why did her cells keep growing?

    She must be still alive.

    Posted by FigureSkate4Life on February 1,2010 | 09:18 PM

    It sounds like some people didn't read the article very carefully. I can't find where Rebecca Skloot is white in it. The story is way cool.
    People must be kidding around when they use words like "vampire". Henrietta's cells are not any different than anybody else's, they just were the first to survive back when they were harvested.
    Whether or not the family should be compensated is up to the courts. I would be glad if they did. They were a very handsome couple and I'm sure very good people.

    Posted by Joel Jaworowski on February 1,2010 | 09:19 PM

    Today, when you consent to entry into a medical study you are asked to read about the protocol and ask any questions that you have and 'consent' to the medical treatment. That seems like an obvious and very basic tenet, but there were decades in which scientific studies like the Tuskegee syphilis experiment were run. This is a similar case. Today, you would be explicitly told about the medical intervention (if any) and how your materials (cells, blood, stem cells) would be stored and/or used in the future. You are told that you are signing away those materials for science and are not allocated compensation should any medical breakthrough be made based on your sample(s). Unfortunately, these regulations were not in place at the time that HeLa underwent cervical surgery and her tissues were removed (as per the surgical intervention) but were then transferred to another party without her knowledge or consent.
    Normally, cells divide (make reproductions) about 40 times (generations) and then go into senescence until they die. The number of times that the cells multiply is based on areas at the end of the chromosomes within the nucleus of the cells. These areas are called 'telomeres' and a little bit of this area is lost each time the cells replicate. The cells stop replicating before the chromosomal loss gets into areas of important genetic material on the chromosome. Immortal cells, like the HeLa line, have the capability to adding to their telomeres so that they don't shorten with each replication and continue replicating continuously (think of this like a tumor that keeps growing).

    Posted by Melodavis on February 1,2010 | 09:19 PM

    We are who we are, and the cells has a very potential part in our bodies , they do reproduce and grow .This story is amazing and very significant for all the humans, doesn't mater nationality, race or color, The most important part is how many good things they had done with this cells. The sad thing about it is that her family or her never knew about this until later after she past away. The researcher did a wonderful job and to end this . GOD BLESS THIS BLACK WOMEN and all her living cells for ever. RIP HL

    Posted by Mercy on February 1,2010 | 09:19 PM

    Once more the unforgetable role of power lift it ugly head. Yes the family has a right to some form of compensation. History is full of events such as this and simply because black people had no rights and no power. I would love to have the book.

    Posted by Arthur D. Truss on February 1,2010 | 09:19 PM

    I find this truly fascinating, though it disturbs me that to hear that doctors/scientists acquired the cells in an unorthodox manner; not notifying the family or obtaining their consent. The Tuskegee experiment immediately came to my mind. For those who feel that Henrietta Lacks' family should be more altruistic and look beyond monetary compensation; I say phooey! It's not all about money, but it IS about money. Even if we concur that the end justifies the means, why should so many people make billions of dollars from the sale of this woman's cells, while her family lives in poverty. May this woman rest in peace and may her family find solace in knowing that she made such an enormous contribution to the world.

    Posted by Hazelin Williams on February 1,2010 | 09:19 PM

    It is very funny people are saying thay there is no need for compensation. People charge to use their male dogs in breeding and no actual work is involved by the person. I do not know of a Dr that works for free. I have to pay for my vaccines. They are not free. They took advantage of her family. They even had them come into check to see if they had cancer but actually they were checking to see if they had the immortal cells like their mother. It is very sad. I hope this really gets mainstream so the family is compensated. I will not purchase the book unless the family gets roylaties from it. Most likely it will be the have (the author) getting paid on a have not (the family). All over again.

    Posted by Eve on February 1,2010 | 09:19 PM

    Wow amazing! doesn't this bring an awareness in us that the creator is great.also that soul is what matters and not the physical being.I wish I could buy the book soon. it's sad though that some compensation was not paid to the donor of the tissues (it was obtained by the researchers in the most unethical way, was it 'coz HL had no voice or the discrimination of another sort even at that year of 1951?)Anyway my congrads for the team who found the medical discoveries through this.My heart-felt wishes for the author and the daughter-Deborah.( I can feel her pain) wish success.

    Posted by R. Abdeen on February 1,2010 | 09:20 PM

    Excellent story! Very interesting to the very end! I really wish that it was a happy ending for the family in which they should get compensated! It would be the right thing to do! Then this story would go beyond excellent! Thank you for such an great story and sharing it beyond just science...but with us all !

    Posted by toni on February 1,2010 | 09:20 PM

    This is AMAZING!! This is AWESOME!! The story is just WOW!!

    Posted by Jeaux Ree on February 1,2010 | 09:20 PM

    This was an incredible article.These medical facts are astounding.This woman was a true merical,To see all the breakthroughs in medicine that dew to to her.We may have never gotten to the point we are with treatment and research, without her cells.

    Posted by Velva Guthrie on February 1,2010 | 09:21 PM

    This is a very interesting story! I never knew there was such a thing as "immortal" cells....it sounds like something out of some sort of science fiction novel.....

    Posted by Minerva on February 1,2010 | 09:21 PM

    well. why would the medical profession choose to culture unhealthy tissue??

    Posted by julie on February 1,2010 | 09:22 PM

    This would make for an interesting mock debate for my high school Biology students. Are Henrietta's family members entitled to financial compensation or are the cells and resulting products the result of the scientists who worked with and modified those cells?

    Posted by janelle on February 1,2010 | 09:22 PM

    great!!! now everybody knows who caused our diseases and ola, they got the cure.........great business hah........god forgive us.

    Posted by felix on February 1,2010 | 09:22 PM

    wuh!!!very interesting! wish i could buy the book.

    Posted by Camille on February 1,2010 | 09:22 PM

    Often in my life I've heard of stories how Black people have played a vital roll in our society becoming what it is today. weather or not it's said as at the hand of the white man or as Harriet Tubman's roll and too many other's that seem to flee my mind. However I hope this story is recieved by all as it should be, Henrietta Lacks should be thanked by all for her sacrifice for mankind! We all need to learn to get along a little better, our future depends on it!

    Thank You Lack's Family and Rebbeca Skloot

    Posted by Michael Lee on February 1,2010 | 09:22 PM

    Her cells were immortal because they were cancer cells, taken from her cervical cancer. It was special because it first revealed this information. If scientists have to pay now for these cells, they would simply switch to using cancer cells from a volunteer instead.

    I agree that the family should be compensated somehow for HeLa cells being taken without permission. However, who pays? The scientists that took these cells are likely dead by now. It was unlikely that they even broke any laws at the time. Research regulations were pretty non-existent at the time, so it wasn't as if they were breaking laws by taking her cells since they didn't hurt her when they did it (squabbing the cervix like in a PAP smear to get the cells). Today, that's a different story, but we can't go back in time and punish people for breaking today's laws. If you demand money from scientists today for use of knowledge derived from these cells, what about the patients that benefited from the knowledge? do you charge them too? We're not just talking about drug companies making money here, but also academic researchers who get funding from donations and federal tax money.

    Posted by irisine on February 1,2010 | 09:22 PM

    wow i must readf that book ..... it is very interesting...

    Posted by pooh on February 1,2010 | 09:23 PM

    Assuming the DNA will be traceable, I still say, Adam & Eve were people of color!

    Posted by Rolf Slade on February 1,2010 | 09:23 PM

    Wow, what an awesome author. Thank you, I am adding it to my collection tomorrow. Keep writing. (smile)

    Posted by Grace Wright on February 1,2010 | 09:23 PM

    Very interesting great article i will definetly will seek for that book. Thanks a lot.

    Posted by Irene on February 1,2010 | 09:24 PM

    This issue was also covered in Micheal Crichton's book, Next.

    Posted by debbie on February 1,2010 | 09:24 PM

    This was done to help mankind,many samples were submitted,all types of people.

    Posted by marlo d luttrell on February 1,2010 | 09:24 PM

    Very interesting ...I do believe the family should have compensation since there was never permission given ...what a great story ...we all owe Henrietta Lacks for her unknown cotribution!

    Posted by debem on February 1,2010 | 09:24 PM

    good story

    Posted by to cool on February 1,2010 | 09:24 PM

    There's much info missing from this story. Her story has been known for a while & there is much missing from this version. How about the fact the doctors were actually the ones who gave her cancer in the first place? They were "harvesting" cells and such from black women as an experiments. They were trying to understand many mysteries like how could the limbs of blacks whose lost limbs after sometime could begin to regenerate. The answer is and will always go back to the black woman. She is the key and the DNA mapping will trace everyone on this planet back to the original origin of the black woman.

    Posted by MA'AT on February 1,2010 | 09:24 PM

    I'm sure if you bought the book, half of your questions such as "was her family compensated" etc would be answered.

    Posted by Boli on February 1,2010 | 09:25 PM

    I personally believe the family should be proud that their mother has given so much even after her death. If there is any profit, then, yes, the family should receive funds. If we all should have such a legacy after our death, it would be a better world. A great article.

    Posted by TBounds on February 1,2010 | 09:25 PM

    It's unbelievable! Totally amazing! did the family lacks got any residual income from this? Is this real or just a story. Now i'm curious about this book.

    Posted by Wenelyn Drylie on February 1,2010 | 09:25 PM

    What a great story!I would like to know more about this story!

    Posted by Marilyn Williams on February 1,2010 | 09:25 PM

    I learned something. I will buy the book and continue this voyage of new exposure to something old and hidden.

    Posted by Ed on February 1,2010 | 09:26 PM

    Thank you, Ms. Lacks.

    Posted by Lloyd Llaga on February 1,2010 | 09:26 PM

    She is of the human race,but note she also carried in her the gene pool of a race of humans scientist coined "the original race".Which in time carbon copies would mutate a billion times changing each time. (and here we are)

    Posted by Al. E. on February 1,2010 | 09:26 PM

    there was no intent at the time to profit from the cells that were taken. the fact they lived was great and modern medicine benifits The family should be proud! although I think any profit made the family once there cells helped in research to learn more about the identification of her genes, there should be compensation passed on to the family, Black or White doesn't matter to me, but the education is.

    Posted by Ray Heeren on February 1,2010 | 09:27 PM

    Amazing Story!
    Sadly to say I don't feel that the family should be intitled to anything. Sorry C.Frasier. Work for a living.

    Posted by John Dalton on February 1,2010 | 09:27 PM

    Nice story…Only it's sad that most comments are more about financial compensation to her family than anything else. I think that misses the central point. The most important thing here is neither money nor the fact that she was black, but rather the very important implication of the immortality of her cells, which can potentially teach researchers how to make all cells behave in the same manner...Am I the only one you Can imagine the end result?....immortality people...And instead we are focusing on the lady's race and how much money she got or didn't get..

    Posted by John Audidge on February 1,2010 | 09:27 PM

    Very interesting...makes me wonder what my cells contain. Medicine has come so far within the medical field that I am proud to say...I'm glad I chose this profession.

    Posted by Rose on February 1,2010 | 09:27 PM

    Will someone find out if the family got any compensation or if they donated any of their tissiue sample.

    Posted by shirley williams on February 1,2010 | 09:27 PM

    First of all, the money thing is ridiculous. Her family doesn't deserve a dime, just I like I don't deserve a dime for donating blood. They took a biopsy to determine if it was cancer, and some of those cells went into a dish and were grown. As the court decided, those cells were to be thrown out anyway.

    Second of all, the reason the cells never die is because they are CANCER cells. That is what cancer is, cells that never die. They are immortalized. That is why they kill you. They grow out of control and take over tissue.
    In this day and age if you want to immortalize a cell line, you basically turn on the cancer genes to do so. So no, she is not a vampire, not a freak, not unique, and not an immortal. The woman had cancer like more than 50% of us out there, and if you took any of those cells and put them in a dish, there is a good chance they would keep growing too. The author of this article should have explained this better. Any cell line can do this if programmed correctly.

    Lastly, it is no wonder our country is so bass-ackwards. Journalists who are trying to explain science don't even know enough about it to teach it right. It is like the blind teaching the blind. Now we have ridiculous museums dedicated to biblical science instead of evolution, and worse, we used to have a president who supported that. Enough people. Start reading real books about science. Use wikipedia. Use google. Learn and stop living in the dark ages. We have come so far, but some us would rather pretend it has never happened and go back to sandals, digging for water, and living in huts.

    Thank God we have a president who now supports the NIH and science. That is God people!! That is where he/she lives. It is in the science. Learn and understand how it works and you see the glory/beauty of it all staring back at you. That is the gift for us. If more would see that, there would be less killing for religion. Less wars and less morons out there.

    Posted by Dan on February 1,2010 | 09:27 PM

    The photo makes it obvious that this wonderful lady was of mixed blood. When are we idiots in this country going to get off the kick that if one has any black blood they are completely African. Maybe the miracle of her cells resulted from the admixture of black and white genetics. Has any non racist genius considered this?

    Posted by Kurt on February 1,2010 | 09:28 PM

    OK, I had cancer, and if tissue taken from me not only outlived me but helped people, I'd be very happy in Heaven. I guess I'm not getting the problem.

    Posted by Bill S. on February 1,2010 | 09:28 PM

    agree w/@Fraiser above. The "immortal-part" is 'cause they grow um like wheat in a field, only it's a petri dish? And no mention of the "generational-aspect" Is the current "batch" first generation? is someone in possession of the actual tissue sample or whats left of it? -or- did you multiply the hell out of it 1000 generations ago? I can't help but think some poor-people should get some buckets of ducats!

    Posted by maxam on February 1,2010 | 09:28 PM

    WOW! I'm not a big biography fan; more of a science fan, but this book is just begging to be read. Was a little confused about the use of the word "poor" in her description but the pic with the article seems to show a woman very well dressed for the time period. Nonetheless, how can anyone put a price on her contribution to science? Maybe her immediate family should receive substantial recompense from every major drug company in the world.

    Posted by Bocephus Montgomery on February 1,2010 | 09:28 PM

    This was a very remarkable story. Thank your for sharing it. God Bless you for your perseverance. Much success on your book!

    Posted by DR WILKINS on February 1,2010 | 09:28 PM

    I just find the story hard to belive

    Posted by Linda Fay on February 1,2010 | 09:28 PM

    Great article! Sonya Armfield

    Posted by Sonya Armfield on February 1,2010 | 09:29 PM

    I plan to buy the book. I think the doctor who took cells in the beginning was trying to understand her cancer and therefore help her. I don't think the family should get any money, they didn't do anything to earn it. Afterall it was only a few cancer cells, that would have been discarded anyway. The woman was beautiful and she inadvertly gave to medical science; let it go at that. Afterall many people today, donate their entire bodies to medical science when they die, and no one gets any money.

    Posted by tim womck on February 1,2010 | 09:29 PM

    To Deb Carlsen's remark...it isn't SOMEONE somewhere who owes this woman, but EVERYONE who's ever gotten a polio vaccine..

    Posted by Iryshprincess on February 1,2010 | 09:29 PM

    This is very interesting. I would love to see more pictures of her along with family members. I hope the family get compensated.

    Posted by Tena on February 1,2010 | 09:30 PM

    Great story but nobody is owed anything. It was friggin 1951 and the doctors extracted the CANCEROUS cells of a dying woman. No longer is it good enough to receive credit for saving the lives of millions; no I need my handout. Good luck suing *everyone*.

    Posted by whatever on February 1,2010 | 09:31 PM

    A beautiful story about a beautiful woman she has indeed left her mark on the world whether she knew it or not. I hope the author and the scientist do the right thing and compensate the family for their contribution to the world.

    And to you few sickos who think the vampire name is funny, you are out of place and oh so wrong. You ought to be thankful that you were able to benefit Mrs. Lacks suffering.
    God Bless her family!

    Posted by Ruth on February 1,2010 | 09:31 PM

    great story! vEry amazing..

    Posted by emma estores on February 1,2010 | 09:31 PM

    AMAZING! More researches as interesting as this should be published and told. I'm teaching research in a university in the Phils. and I'm going to share the story to my students. I'll buy the book too.

    Posted by Marie Frances Buyco-Macabenta on February 1,2010 | 09:31 PM

    Very interesting, would love to read the book! I am listed as an organ donor on my drivers license and that means "donate" not sell my organs, tissure, etc. But they have my permission and that makes a difference. It is a very different and more enlightened world we live in now.

    Posted by Dolores on February 1,2010 | 09:31 PM

    I heard about this when I was in undergraduate school however, I never saw a picture of the woman and to know that anyone in her family is still alive is awesome. Her relatives should be compensated, BIG TIME.

    Posted by linda tart on February 1,2010 | 09:32 PM

    As a scientist involved with cancer research in one of the world's best cancer research institute, I feel obligated to contribute on this issue. HeLa cells have been used extensively in scientific research. Currently we do not use HeLa cells any more, as we have learned that due to accumulation of mutations, all the biological processes are somewhat not controlled in those cell lines. Nevertheless, this does not make the contribution of HeLa cells any less. Most of the cancer cells are immortal and are useful in research.

    For the betterment of science, I think these cells/cell lines should be donated and not sold, because the results benefit humanity as a whole. I hope the author has included the scientific aspect in her book too. Otherwise, I fear, it could be misleading for a lot of people.

    Posted by Sid on February 1,2010 | 09:33 PM

    The ignorance the author spoke about is nothing compared to that of some of the comments posted here. I suggest if anyone is interested to begin by looking up both Henrietta Lacks and HeLa on Wikipedia.

    As for the issue of compensation - if I had a cancerous growth and scientists took a sample of it and the cells in question eventually ended up being used to aid research that has helped saved millions of lives - well, that's more than enough compensation in its own right, at least to me.

    I live in a 30' long mobile home and am quite poor, but I know without a doubt there are far more important things than money is this world. With all the medical advancements that have been made using HeLa cells, I'm sure many of Henrietta's descendants have benefitted medically (or even had their life saved) from a medical procedure developed by the use of HeLa cells. Isn't that a far more important "compensation"?

    It's just another example of the greediness of relatives when a deceased person is concerned. Come on, if they'd asked Henrietta if she minded if they analyzed & experimented on her cancerous cells in hopes of helping other people years later, do you think she would have said, "Only if you pay my children a ton of money."

    If you donate your blood to the Red Cross and they develop a cure for something hideous disease from it, and thousands of people are alive because of that, would you start screaming you wanted money?

    Henrietta made the initial "donation" of something she didn't want in her body to begin with, something that ultimately killed her. But she didn't have the knowledge to do anything with those cells. She didn't spend numerous manhours using the cultured cells to develope cures. I find it highly doubtful that if she were alive today she's want anything at all for her contribution. Apparently at least some of her children have; that "the world owes me" thing which so many people get - and very fortunately I personally do NOT have.

    Posted by Me on February 1,2010 | 09:33 PM

    I just picked up the book from a local bookstore, I was surprised that I was able to get it since the book isn't due to release until tomorrow. What I have read so far is very fascinating! I can't wait to finish the book.

    Posted by Ms. Santi on February 1,2010 | 09:33 PM

    Why so much concern about compensation? How do they know that the family didn't know they took the cells? Even the story indicates that her husband didn't understand when he received the call about obtaining DNA. If she was in the hospital, maybe the doctors treated her and didn't force the family to pay after she died. They have her cells, but they wouldn't have survived without the scientists. Everyone is looking for a fast buck, but they don't think there could be more to the story than has been told here.

    Posted by Gary on February 1,2010 | 09:33 PM

    Please keep me informed on what course the family took, and if they receive any money and from whom. thanks Marcus GT

    Posted by marcus Garvey Thompson on February 1,2010 | 09:34 PM

    I would like to convey that the research that you did was very good. It was nice that you did involve her family in the way that you did. I do believe that it would be nice if the family was compensated for the use of her cells. Also, all of you remember that at some time in life as we have today research has to be done to understand how things work and how to find a cure for a lot of things. I am interested in reading the book as a lot have stated. Great article and the public, I think appreciates you doing what you have done for the family also.

    Posted by David McCranie on February 1,2010 | 09:34 PM

    What a great story ! However I think I am losing something here. Are her cells the only ones that continue to live,and are we being told that her cells can never die or never be killed. If so, then they should carry the secret to ever lasting life. and if that is true then what an amazing scientic discovery that would be. Especially from a black woman who represents her race that was at one time treated as non humans and hurt in so many ways. They are an extraordinary,talented, loving, caring, strong, soulful group of people that we are connected to along with every other living life form on this planet. We are all part of ONE LIFE, a Universal source of never ending power that is everywhere present in all places and every place at all times and any time, therefore this power has to be where we are every time of NOW. We all know it as a God power. My blessing to her and her family roots,......I wonder !!!! Did the Universal Source put those cells in her to some day change how people can live in a world without hurt and pain inbedded in our souls. A day when like the leaves on a tree never battle with each other but live together in harmony to provide the oxygen we humans breath to keep our hearts beating and all of us living.

    Blessings and love
    Rev.Dr. Robert

    Posted by Rev.Dr.Robert on February 1,2010 | 09:34 PM

    I and my colleagues are working on an exhibit for our science museum on the West Coast. We just put the rough prototype out on the floor for two days this last week and talked with visitors about their reactions.

    We have live HeLa Cells on a microscope blown up on a monitor and a photograph of her, text about her story and the contribution her cells have made. We also included a small bowl of flowers as an experiment in being devotional in a secular way to the powerful story. So many of us may be alive because of them. We also included a number of questions for visitors to contemplate about who owns your cells and tissues, and whether those cells are you. We also pointed out some unique features for visitors to look for in the live culture, including the fact that they often have two nuclei and you can see this.

    The prototype is for a collections of exhibits about things that are at the intersection of science and society.

    Visitors reactions to this first prototype were tremendous and their comments very insightful. The experience was gratifying -moreso than this can usually be. Many had never heard of this story but a few had. One gentleman told me "This is science but it's bigger than science. It's part of my African American History."

    I first heard of the cells from a staff biologist last summer. She encouraged me to try the exhibit and grew the cells for me. And when I was researching the story to develop the idea and text I read about your book and was very excited. I cannot wait to read it.

    Thanks for this great article.

    Posted by Melissa Alexander on February 1,2010 | 09:34 PM

    First off, get a life. Most of you are more worried about compensation to the family. If you had ever had surgery, women a pap smear, everyone that has had blood taken or given blood, how do you know that it wasn't used for research,how do you know wether they found something that could help someone else. I just finished medical school and I have found this story extremely interesting. To bad I didn't learn about the HELA cells. Whether the cells were taken or given should not be an issue. They were used for research and saved lives.Science isn't always about money. Yes I agree that there are probably cures that we are being told about, and yes pharmaceautical companies are all out for the money, but we as human beings should be helping one another, in any way we can. They can have any part of me , if it will help someone else, with no compensation to me or my family. This is my body, not theirs. No one owns me but me. And I feel that that Mrs. Lacks would have given consent. It's to bad they didn't have a cure for her back then. I was born in the fifties, my mother had B- blood, while I had B+, we were killing each other because of the RH factor. It was years later, that they found something to help women without the RH factor in order to have uncomplicated births. This country is filled with greed. Now, how can we fill it with love and giving of one self to another.FREE, no charge. I feel for the daughter never knowing her mother, but with the research done on her mother, she now knows more then she did before. Mrs. Lacks cells helped many people, God Bless her. Be a person Black, White, Red, Yellow or what ever color, we all live together on this world, and as such should help by donating any part of you to science, in order to help the next generations; your children, grand children, great-grand children and so on. Knowing your heritage is more important then how much money you can gain from it. Help science, Donate.

    Posted by Tigger on February 1,2010 | 09:34 PM

    Interesting.. huh

    Posted by Soji M. Balbin on February 1,2010 | 09:35 PM

    It is interesting to observe the following from the comments:
    - How the readers are applying TODAY's standards to practices done 50 years ago, when informed consent was not considered and science was done primarily for advancement of human knowledge and for the greater good. Big money in biology? Only in the last 20 years.
    - How even in this article aimed for non-specialists misconceptions happen, such as "We are talking about the 1950's aren't we?! Ironically white Americans were unaware that a Black womans DNA was being used in vaccinations that Im sure the majority of Americans received. I think that's the reason for the secrecy. People would have rather died of Polio than received a drop of black cells injected into their bodies." Communicating science accurately in everyday language is not easy.
    I recommend the article PLUS the comments as reading and discussion materials for a biology, science and/or bioethics class.

    Posted by ida on February 1,2010 | 09:35 PM

    What a great story about what was apparently a remarkable woman and her family. Please post when/where the book will be published. I'd love to read more about this fascinating subject.

    Posted by Angelia on February 1,2010 | 09:35 PM

    Indeed an interesting piece; however, it's within the human experience to speculate when truth is hidden. Man's search for a panacea to diseases and illnesses that plaque our existence will no doubt continue as we evolve. That's not to say that we will necessarily change physically but the sum total of knowledge we accumulate throughout time will inevitably allow us to find cures for diseases while we continue to reach for immortality down the wrong corridor.

    Posted by OmoOran on February 1,2010 | 09:36 PM

    See this is the problem I have with black history month stories. What you didn't say is that not all HeLa cells are from this woman. It's just the name given to cell lines that don't fizz out. Which btw is true for most cancer cell lines when properly handled. There were black men and women who actually did things. George Washington Carver for example. I am really sick of hearing people praised for their 'valuable contrabutions' when in fact they did nothing or simply broke the law or rules of a business. And live human cells do not 'float though the air'. Dead human cells can, viruses can, but not live human cells.

    Posted by trinity on February 1,2010 | 09:36 PM

    Wao!! Incredible story!!

    Posted by Hannette on February 1,2010 | 09:36 PM

    http://www.amazon.com/Immortal-Life-Henrietta-Lacks/dp/1400052173/ref=sr_1_1?ie=UTF8&s=books&qid=1265078153&sr=1-1

    Posted by PatOrgas on February 1,2010 | 09:37 PM

    Good job!You have just made the family aware of these important things in their lives. This is going to be a great start for Hela's family.

    Posted by Lailah on February 1,2010 | 09:37 PM

    Although it is years later, what a blessing this story is!

    Posted by Angela on February 1,2010 | 09:38 PM

    Company takes personal property without permission and makes billions, trillions, for itself and other medical based companies like itself.

    The doners get nothing.

    Health providers and reciepients pay exhorbetant prices for these wonderful ground-breaking cures and, as is the case with some biologics; patents may never run out(no generic ever) insuring that top dollar be paid at all costs (pun intended) by those in need.

    Now we are getting to the bottom of why we have to pay so much for health care!

    Posted by Ian on February 1,2010 | 09:38 PM

    my mind stop for a while,,,speechless...dnt knw wat to comment..btw,,it was a nice story and i begin to search hela cells...

    Posted by lhot on February 1,2010 | 09:38 PM

    I would be proud to know that my mother has helped many people through-out the years. If this woman was found to have cancer now she'd likely for many more years.

    Posted by Gail on February 1,2010 | 09:38 PM

    I found this quite interesting because it was only a few months ago in AP Biology that my teacher had talked about Henrietta Lacks. However, she had not mentioned anything about her cells living "forever," as scientists put it. There is no way that cells can live forever because their only way of reproducing is through mitosis, which is the division of cells into two identical daughter cells with identical genetic material in both cells after cytokinesis. Now, as we learned in class, every time a chromosome, protein and DNA coiled tightly together, duplicates, it loses a little bit of the tip of the chromosome, containing bits of information. Once the cell has divided so many time, this part of the chromosome wears off, causing the cell the die. This is only one reason that cells cannot live "forever." As we grow older, our cell division rate begins to slow down because our bodies become weaker and the growth of the individual usually stops at around the age 18-20 in height, but muscle mass usually continues to grow as the individual continues to live his/her life. Therefore, I do not believe that scientists have really found a way to make cells live forever or even claim to have discovered these "magical" cells. There is just too much evidence to go against this theory.

    Posted by Berta on February 1,2010 | 09:38 PM

    Wonderful jounalism.Also have a good look at their picture,for a poor farmer to appear so well lived,then most so called rich americans today are indeed actually poor now,but living in self deceit.Kudos Madam Sarah Zielinski.

    Posted by Danladi on February 1,2010 | 09:38 PM

    Granted, her family should be compensated. But come on, no one did anything malicious by "stealing" her cells. They were cancer! Ya' think she wanted 'em? Some of you need to mellow out.

    Posted by Larraine Taylor on February 1,2010 | 09:39 PM

    the story about hela cells. the story that you are writing is so great ... i want to know more about Henrietta.. :)

    Posted by jah on February 1,2010 | 09:39 PM

    Wow. This is an intersting story. I can not wait to read the book. I also believe her family deserves something.

    Posted by Brittany on February 1,2010 | 09:39 PM

    Just guess, Think you can put a number on how many lives the HeLa cell alone has saved?

    Posted by L. Gonzales on February 1,2010 | 09:39 PM

    Thank you Rebecca Skloot. Science,medicine and money without moral obligation.

    Posted by Ariffin Dom on February 1,2010 | 09:39 PM

    This is truly wonderful...here is another major contribution to mankind made by a black person. Another reason for me to feel so very blessed to be born black. The contributions made by so many that benefit so many is truly Awesome and all ethnic groups are the benefactors. So yes, the family should be compensated on one hand but on the other hand sometimes compensation is "Priceless". Mrs Henrietta, thanks for your contribution and being an Angel watching over us all...

    Posted by Maxx on February 1,2010 | 09:40 PM

    There is enormous interest in this book. Please give us information on its distribution so that we may acquire it please.

    Posted by Perry Burnham on February 1,2010 | 09:40 PM

    Nice piece! Knowledge is power. To an above comment this incident is still occurring today when you go in the hospital they keep a lot of things. Ways of man.

    Posted by Diamond N the rough on February 1,2010 | 09:40 PM

    So a congratulations to the family of this amazing woman and second.............Are we supposed to trust all doctors after hearing a story like that.......NOT FAIR AT ALL!!

    Posted by Slimm G on February 1,2010 | 09:40 PM

    @Colleen

    No, the HeLa cells are immortal, they continue to replicate-- they are also cancerous, which is one reason they are able to keep living in culture.

    In fact, normal healthy human cells will not live forever and can only divide a finite number of times (called the Hayflick limit).

    http://en.wikipedia.org/wiki/Hayflick_limit

    Interestingly enough, that some scientists are studying how to prevent a cell from reaching the Hyaflick limit in healthy cells (non-cancerous, like the HeLa cells) as a way to study aging and death.

    Cheers

    Posted by Mary on February 1,2010 | 09:40 PM

    WOW, amazing story, makes me want to go out and donate cells,

    Posted by Chris Harris on February 1,2010 | 09:41 PM

    This article made me realize that cancer, the disease that stole my mum, has its end...

    Posted by Emelyn Flores on February 1,2010 | 09:41 PM

    I hope the family is compensated. They should be very honored at how much help their mother has given to research, but the researchers should be ashamed for not telling this family about the fate of their loved ones cellls

    Posted by valerie on February 1,2010 | 09:41 PM

    If scientist are able to develop all those medical advances utilizing cells of a sick woman, and frozen for 60 years, what in the world do they need cells taken out of embryos to do research?
    There's no excuse for all those killers working in "the name of science". It has been proven that cells can be used and reproduced by simply using those of the wasted placenta after a mother gives birth. Wake up everyone and open your eyes.
    And Henrietta, even if unknowingly, we all owe you a lot of thanks. Hope your family receives some kind of compensation.

    Posted by sigpad on February 1,2010 | 09:42 PM

    Very interesting article. Makes you wanna think what else did they do back then behind people's backs. I would want to buy the book and read the whole story. I also want to knwo if the family got compensated for what was their right?
    Great job to Rebecca Skloot!!!!

    Posted by Rushina on February 1,2010 | 09:42 PM

    HeLa cells are apparently defective human cells. A while ago, researchers found that human cancer cells from all types of sources were mysteriously transformed into HeLa cells. These were cell cultures that had "transformed" themselves into HeLa cells. (info from Howie XXXXX).

    Speculation: Helen, herself, probably never had HeLa cells!?

    Posted by curt on February 1,2010 | 09:42 PM

    Really not surprised since the DNA of all human life has been traced back to one Black Woman on the Continent of Afrika! The real life "Eve"!

    "Without the Mother - there is no child." Wisdom Statement

    Posted by Askari on February 1,2010 | 09:42 PM

    I enjoyed the article so much! I always have liked reading History! Very good!

    Posted by cathy on February 1,2010 | 09:42 PM

    As it was then, it still is now, all "materials" removed by a doctor or hospital is the property of the doctor or hospital.

    The woman was a blessing to us all and we should all be very thankful for her unknown contribution. As for the contributions sought from her family, since they were by request, should have been fairly compensated.

    It is sad that this woman was buried without a marker on her grave as the family being so poor. Too bad that those that have profitted so much could not at least give her that honor, and perhaps do something in her name to keep her memory apparent.

    Posted by kris on February 1,2010 | 09:42 PM

    This is one amazing story. This family deserves what ever comes to them in the future. May God bless you all.

    Posted by A.Moultrie on February 1,2010 | 09:42 PM

    Absolutely compelling and breathtaking...honestly, this article has completely captivated me...I can't wait to share it with my Biology professor...

    Posted by Jini on February 1,2010 | 09:42 PM

    Quite an interesting story. However, it's just as interesting to read how many people responding seem to focus on compensation for an act that happened almost 60 years ago. Fortunately, we don't have to go back and find the family of the caveman who invented the wheel. We have ALL benefited from this research in different ways. Why does someone always need to be sued in the America of today? In todays world I'm sure it would have happened differently.

    Posted by Tim Hollenbaugh on February 1,2010 | 09:44 PM

    Just Amazing! Best article I've have read.

    Posted by Romell on February 1,2010 | 09:44 PM

    I think it is proof that we should live forever... Beyond Cool..I'm looking forward to reading the book.

    Posted by P. Bogema on February 1,2010 | 09:44 PM

    It seems that the doctor specifically tried to hide the identity of this woman which is deception. because she was a black woman many people in the 50's would have shunned the experiment. this has to be looked at in many different perspectives. because they went to her family looking for more answers then they should have been told what's going on. as for the money its a toss up. how many of us has dna or genes being experimented on now. are we looking for compensation. we all know that doctors and scientists experiment on the samples given to see what is causing the problem. the brothers didn't care until they heard billions and then it was a problem. perhaps they should be compensated after all they did come looking for henrietta's family for more samples.

    Posted by glenda on February 1,2010 | 09:44 PM

    Who did more for humanity? The woman, or the doctor who collected the cells? There is merit in being tall, or black, or white? Where is intentionality in these? What merit is? It seems that you people don't realize what are you talking!

    Posted by Peter on February 1,2010 | 09:44 PM

    Thanks for this information, I wonder how many other have been used this way.. I am glad you brought this out about the use of this womans gift to hummanity and the fact that she nor her family reaped financially from it..

    Thanks

    Posted by R.Jackson on February 1,2010 | 09:45 PM

    Very nice peice. I an researcher and have workred with these cells a lot. I had heard about the story but not in this length. Thank you for bringing it out, it makes me put a face on all those studies that I did on these cells. It also makes me wonder about all other cell lines that we use these days and the stories that might be behind them, amazing!

    Posted by Tariq Hamid on February 1,2010 | 09:45 PM

    Does this mean that we will get to be immortal if we find out what part in her dna caused her cells to be immortal and put in our dna? Even if we could, we shouldn't because then life would lose it's value and we wouldn't have enough room on earth to reproduce and still keep the other people, it's the circle of life. BTW: how did she die?

    Posted by Cheyenne on February 1,2010 | 09:45 PM

    This is an amazing and interesting story which may give clue to the origin of man kind. They should also investigate whether the family members have the same gene with their mother or not.

    Posted by Mohammed on February 1,2010 | 09:46 PM

    I hope the family got some compensation, but somehow I doubt it. The way of corporate, greedy America!

    Posted by jill on February 1,2010 | 09:46 PM

    To all those stating that "others donate their cells without compensation" and so on- read exactly what you said- donate. My mother donated her organs, she willingly gave consent. And for all those that donate they can also choose the purpose, research or to implant in others. Henrietta, again, was not given this choice.

    The racial issue here, is one that was prevalent at that time and still goes on. Just because "things were different back then" doesn't mean they were right. Taking cells without the donor's knowledge is immoral at any time- just as hanging someone was wrong. The timeframe doesn't justify the actions! What made it a "race thing" is the fact that the actions taken by her doctors were common practice, with Blacks as guinea pigs.

    The fact that anyone contributed as much to society and was able to remain impoverished is also wrong. There are many historic artists, poets, and others who lived and died poor only to become famous postmortem- it would be just as wrong if their families never received any compensation from their worldly contributions- and remained to live poor. That's wrong. With so much money in so few hands- no one should be living the way many do today, noone should go hungry, homeless, etc... because so much wealth is there and being hoarded by greedy liars. Thank you to all the rich that try to spread the wealth and make the world a better place.

    Posted by Think before you speak on February 1,2010 | 09:47 PM

    If there is one henrietta out there, their has to be more henriett's cells of other people floating around out there in some other labatories here in this country and in other countries.she can't be the only one out of 6 to 7 billion people are more on this planet.

    Posted by daffy22 on February 1,2010 | 09:47 PM

    Very fascinating article! If the cells live forever, then could it be possible that a human could live forever?

    Posted by sag on February 1,2010 | 09:48 PM

    What a wounderful discovery. Most things that have been discovered accidently have been for the good. I have a chance to see blood from umbilical cords and one day a drop of blood from a cord from a 33 week preterm baby fell on a piece of paper the small drop of blood organized itself and actually formed tiny vessels resembling the bottom of a leaf it was amazing. I believe some of the human race( all colors) carry the secret of living for ever, watching these blood cells(stem cells) was also as amazing as the discovery of this womans amazing cells and the discovery of dna KNOWLEDGE IS POWER lets use it wisely :)

    Posted by cj on February 1,2010 | 09:48 PM

    I have used HELA cells in the laboratory, propergated them, frozen them and grew viruses on them I hope the family gets compensated. Yes I would like the book if I could find it

    Posted by Margaret Tagwira on February 1,2010 | 09:48 PM

    I worked with Hela cells when I was doing cancer research. They were indispensible and yes they were hardy cells that grew readily and continuously. Someone said earlier "why should the family get compensated. Less than a teaspoon of the cells cost $300 several years ago. Why should a company be the only one to benefit

    Posted by Cheryl Benion on February 1,2010 | 09:48 PM

    I am just curious how a certain cell that has lead to a lot of scientific landmarks including vaccines and cures for many diseases is actually a cancer cell. Could it possibly be the key to curing cancer even if its host died of cancer?

    Posted by GerryL on February 1,2010 | 09:48 PM

    This was a very interesting article. I usually don't comment on these articles, but this one inspires me to get the book to better understand the significance and total impact this women had on medicine for all of us. I comprehend how the insistence on monetary compensation in each and every case could hamper the progress of medical research. Still I say, owing to the clandestine way that Ms. Lack's cells were harvested, her family deserves something. This would be a meritorious act if only to restrain the unmitigated plunder of the poor and uneducated by scientists. Let this 21st century be a time when Humans of humble stature be educated to donate their cells, tissues, organs, even bones to medical and biological research, development and treatment modalities for the betterment of all mankind....Or am I being too naive?

    Posted by Calvin H on February 1,2010 | 09:48 PM

    When I read the title I immediately called my seven children into my room. We had an on-the-spot history lesson/question and answer session right in my bedroom.
    I would like to praise the author for being diligent - taking what was learned and following thru with it. My favorite part was where the author says " ...I imagined myself writing..." We have to teach our kids the importance of this concept. This writer actually saw themselves writing this article and it did come to pass today and has blessed God knows how many readers. I don't know the outcome as far as compensation but more importantly, I will pray God's will be done in the lives of the Lacks family, the writer, readers and all those whose lives HeLa cells have impacted.

    Posted by Zonnie Adamolekun on February 1,2010 | 09:49 PM

    We all bleed "red" no matter the skin, hair or eye color. One day this world will understand that and the wars over dirt will be forgotten. Isn't it time we get a clue before its too late?

    Posted by Kelley on February 1,2010 | 09:49 PM

    To address a few of the comments and concerns on here, the polio vaccine was discovered using HeLa in testing, so they did not have to inject people with various test vaccines. In biology and drug discovery, cell culture is used to not only learn about the life cycles of various diseases but to see how those diseases interacts with potential drugs before moving to human testing. It is also considered a better alternative to animal testing, which for some human viruses would have to be done in chimpanzees since the viruses do not infect other animals.

    These cells are termed "immortal" because like what has been said, they can replicate and divide forever. There are many mechanisms, including the shortening of DNA that limit the life of a cell to a certain number of divisions. When a cell reaches the end of its life it ceases to divide and undergoes apoptosis (programmed cell death). When cancer is developed the cells change and live long past the time they should have died. They accrue mutations that cause abnormal functions and lead to the disease. Cancer is so difficult to eradicate because the changes to the cells that make them cancerous, cause them to be able to replicate indefinitely. Some stem cell researchers term these changes de-differentiation because cancer cells share some similarities to stem cells, especially in that that can keep replicating without undergoing apoptosis.

    Posted by Scott on February 1,2010 | 09:49 PM

    someone should investigate to see if they cloned sister Lacks.I can see them doing just that.The question would be how many.

    Posted by margaret myles on February 1,2010 | 09:50 PM

    I work with HeLa cells quite often, but never knew the true story behind their existence. Thank you for the story. Great work!

    Posted by Kim on February 1,2010 | 09:50 PM

    wow

    Posted by cristina on February 1,2010 | 09:51 PM

    this is awesome! it kept me interested and i want to buy the book to learn more,.:D

    Posted by pearl on February 1,2010 | 09:51 PM

    Bioethical standards in medical and allied researches in the 1950s were not as stringent as it is today but this is no reason for taking cells without informing the "donor" at the very least. I believe mankind owes a lot to the real HeLa and by recognizing what she had unknowingly contributed is one small way of appreciating the person.

    Posted by En-Ar on February 1,2010 | 09:51 PM

    it's a stunning experience.But the family memeber should be made aware about this matter and get their consent to carry on such experiments.

    Posted by sudarshi on February 1,2010 | 09:51 PM

    This is a wonderful thing for research but since the family knew nothing about it and people became rich from their mother's cells, they should get something for their contribution to millions of people in the world.

    Posted by K. laney on February 1,2010 | 09:51 PM

    Amazing story. The family should get some of the cut- simply because it was done without permission- I would love to read the book!

    Posted by Tammy Mullins on February 1,2010 | 09:52 PM

    As for family compensation, it unfortunately is unlikely this has been resolved as, according to laws, once tissue has left the body, it is considered biological waste and can technically be used for whatever. There has been much examination into these kind of practices, especially in the concept of how far does the ownership of your own cells and genetic material extend. I too believe in informed consent and believe that to an extent, you have a right to at least know and choose what happens to your tissue. As for monetary compensation, that is a very dangerous game to play, especially when dealing with the combination of ethics and legality. Then we start putting a price tag on a human being. If, for instance, my cells contained the only cure for cancer...that cure would be near priceless to pharmaceutical companies and the patients who needed them. What if I only sold them to the highest bidder, rather than those of greatest need? What kind of person would that make me? What happens if others come after me just because of my cells and my life is in danger? Is that fair to me or anyone else? I actually found the fictional work, Next by Michael Crichton, to be very interesting and made me think about the science I was performing in grad school and how people are all affected when you begin to put a price tag on things like cells and genes.

    Also, to any who think this was a "white" scientist making millions off of a poor "black" woman, it is not true. This type of thing was commonplace in the 50's with all patients. Researchers and doctors all want to solve the problems that plague our species. Most likely, some researchers were trying to get some tissues to grow in culture and were failing badly... possibly with their project funding on the line. They ask one of their colleagues, "Hey you have any ideas?" In this case, perhaps a doctor said, "Yeah, I just cut a tumor out of a cancer patient, maybe you could try a few of those cells?"

    Posted by Scott on February 1,2010 | 09:52 PM

    Talk about 'Eternal Life' I pity the poor- for he can not pay his bills. I pity the rich- for he seeks to be richer. Oh that man would share- that the poor will be rich and the rich be APPRECIATIVE.

    Posted by Shelia Jordan on February 1,2010 | 09:52 PM

    Very fascinating peice of history. The family should definitely receive compensation because the tissue cells were neither donated or volunteered for further medical research as such in this case. Many things were done to black people for ressearch both before and after slavery. I am glad that Henrietta's cells did something to promote further advances in human evolution. I wish her family the best of luck in this matter.

    Posted by Boge'e on February 1,2010 | 09:53 PM

    WOW, NICE STORY ITS INTERESTING GOD BLESS YOU

    Posted by carolina dungo on February 1,2010 | 09:53 PM

    Everyone is ignorant of the fact that in the 50's hospitals were for helping people, now they're just multibillion dollar cooperations. Thanks upmc

    Posted by homer on February 1,2010 | 09:53 PM

    What do you guys think about making a film on this amazing true story.

    Posted by Kg on February 1,2010 | 09:53 PM

    ....This makes you wonder what else has been taken and used, by the medical field, without permission or the person being aware of it!!!!! All good things can be made bad!

    Posted by Dee on February 1,2010 | 09:54 PM

    very interesting story. thank your for the new knowledge you have given me.

    Posted by asa on February 1,2010 | 09:54 PM

    nice and intereting piece...good job

    Posted by jun abasolo on February 1,2010 | 09:54 PM

    Her cells were a gift from God. The lawyers, social justice people and the rabble rousers should mind their own business and let this gift from the Almighty play itself out.

    Posted by L. Blasiotti on February 1,2010 | 09:55 PM

    Now those are a TRUE BUNCH of cells. I have worked with them many times.

    Question: Do you know the difference between Hela cells and an embryo in a cellular stage of development?

    Answer: the embryos are NOT just a bunch of cells.

    Posted by DrEdu on February 1,2010 | 09:55 PM

    Weird!

    Posted by zzm on February 1,2010 | 09:55 PM

    Although this story is fascinating, I see no reason to compensate the family. Heinretta is not a hero, she isn't a victim either. The world was different then and we can't go back and correct the mistakes of the past. If her cells made the lives of others better, isn't that enough reward for her family? It should be acknowledged who the cells belonged to but the only real hero's are the scientists who took those cells and made medical advances. She wasn't harmed in that process. If my cells created a cure for cancer, my family would have no right to any money for it.

    Posted by Jk on February 1,2010 | 09:56 PM

    very interesting story..

    Posted by Elvie on February 1,2010 | 09:56 PM

    Oh, I would love to read the book. This is history in the making and I love reading about history. Just wish the family had been found sooner. Henrietta, cells have helped so many, wish I could of known her.

    Posted by Rae on February 1,2010 | 09:56 PM

    Such a touching story, I love reading the headlines and with this particular story peaked my interest a fine piece indeed.

    Posted by marion jackson on February 1,2010 | 09:56 PM

    BRAVO TO YOUR ARTICLE INFORMING US OF THIS LONG JOURNEY TO AID US ALL IN OUR HUMAN CONDITION. RACE ASIDE, WE ARE ALL IN THIS TOGETHER, AND TO KNOW SOMEHOW HER CELLS MIGHT OF HELPED TO US, ALL SHOULD BRING A COMFORT TO HER FAMILY. I HOPE IT WOULD TO MINE. :)))

    Posted by Laura on February 1,2010 | 09:57 PM

    very good story,can't wait to buy the book

    Posted by david britt on February 1,2010 | 09:57 PM

    Bob Beard, I feel sorry for you, you are totally ignorant based on your previous post. Maybe nobody ever dumbed down the concept that people only know what they learn, which typically requires teaching. If you go to a foreign country, without first learning the language and culture, you will have no idea what they are saying or doing. If her husband had been taught about what was going on, he would have known what was going on. The fact that he and his family had been slighted for so long is a tragedy. If only they explained this to him way back then, no one would complain of wrong doing.

    Posted by to bob beard on February 1,2010 | 09:57 PM

    I have prostate cancer and it is likely HeLa cells were used in determining that. They charged ME to take sample (the biopsy) for the lab to test; not PAY ME to do so.

    If they continue using my cells in ongoing research (without my knowledge and/or permission), I would say that is a very important ethical matter. It should be brought to light, discussed and an answer provided with which society as a whole can live with and accept.

    The fact that Henrietta Lack's cells were so used (without her knowledge and/or consent) goes to the very heart of why science continues to stir a huge amount of controversy. It hearkens back to the days when doctors/scientists bought their cadavers (bodies literally stolen from peoples graves) for use in their study of the human anatomy.

    Thieves are thieves, no matter title of distinction attached to their name, no matter their preferred choice of goods traded (or bartered) in on the "BLACK" market!

    The doctor who took Henrietta's cells, stole her cells for research, he was a thief (regardless of the benefits later realized by his act). The family, are definitely owed some form of recompense morally and ethically (if not by law, statute or ordinance)!

    Until the study of the various branches science (which we are now compelled [by law] to accept as being of so great a benefit to mankind) stops doing research in an underhanded and morally corrupt way, and until society chooses to punish those who would choose the corrupt path in their pursuit of knowledge (and generally to further their own reputation and financial means as well), the question of ethics within the practice of medicine (and/or science in general) becomes mute, si long as society permits it to continue.

    Is the controversy in the use of stem cell research today because they use the remains of aborted HUMAN fetuses or because they have stolen them (without the knowledge and/or consent) from the unsuspecting women involved.

    Posted by Mic Hudson on February 1,2010 | 09:57 PM

    Why does this have to be about race or money??? This lovely woman gave her life to cancer, and, UNKNOWINGLY saved many lives! I agree she should have been asked about the samples, however, it WAS the 1950's, and things were different 60 years ago than they are now. This is a fascinating story, and the fact that her name was released is just a fluke! So many people die and leave tissue samples behind. If they could use those samples to save other lives...why not!? Henrietta's family should be proud that their relatives memory (and cells) will live on to help others no matter WHAT their race or social status is! Thank you Henrietta, may you rest in peace!

    Posted by burnett on February 1,2010 | 09:57 PM

    AUTISM: Some of the latest indications are that autism IS from vaccinations, but it's not the mercury (autism increases whether or not the vaccine has mercury). The distinctive is whether the vaccine was cultured on human (cancerous!) cells: DNA pieces go through the child's cell walls, disrupt his/her DNA, and multiply.
    Henrietta's cells may have had more impact on us than even Ms. Skloot realizes!

    Posted by Mike L on February 1,2010 | 09:58 PM

    WOW!!! This is a very interesting story. As a black woman I am very proud that one of my own has such an important impact on science. I have learned of these cells in biology, I had no idea this story was the start of it all. There has been many discoveries behind Henrietta cells, and I am pretty sure there will be more to come. I am very excited to read this book. Thank You for taking intrest and feeding our society with such important and special information.

    Posted by Jessica on February 1,2010 | 09:59 PM

    Here is a site that tells you more about the book. I personally think that I am going to order it through bn.com. But follow this link to the site that tells more about the book and cells. http://www.washingtonpost.com/wp-dyn/content/article/2010/01/29/AR2010012902147.html

    Posted by Nadine Cox on February 1,2010 | 09:59 PM

    It is really a very interesting story. But I am sadden with the plight of the family when the multi-million company is earning much from the cell of Mrs. Lack, the family is leaving in a misery. I hope the gov't can do justice to the family. I want to read this book.Amazing!

    Posted by Nur N. Hussien on February 1,2010 | 09:59 PM

    Although i haven't read the book. Indeed it was a interesting story of innovation on the part of the scientist involved but hopefully not a traumatic experience for the family who were involved.

    Posted by nobody2010 on February 1,2010 | 10:00 PM

    I am supposed to study my anatomy notes but then, this story captured my attention. It is truly worth it to spend some time reading this article. I can't wait to get a copy of the book!!

    Posted by AJ Rivers on February 1,2010 | 10:00 PM

    "Then, as now, there was no requirement to inform a patient, or their relatives, about such matters because discarded material, or material obtained during surgery, diagnosis or therapy, was the property of the physician and/or medical institution. This issue and Mrs. Lacks' situation was brought up in the Supreme Court of California case of Moore v. Regents of the University of California. The court ruled that a person's discarded tissue and cells are not their property and can be commercialized." from wikipedia. Do you people really think her family should be compensated because someone else spent years of their lives working with cells taken from her in a doctor's office?

    Posted by Lisa on February 1,2010 | 10:00 PM

    fascinating!

    Posted by CP on February 1,2010 | 10:00 PM

    This is so cool, but I think Henrietta's family should get some of the money. She was a "part" of them. It's good to hear that lives were saved though. I wonder if other people, somewhere out there, have immortal cells. It could be our key to superextending life. Maybe in a few decades (or centuries) we'll have someone live to be 200 years old.

    Posted by Dakota on February 1,2010 | 10:00 PM

    What a fascinating story. Fiction couldn't touch this one. Could you imagine what we (general public) never hears about?

    Posted by Bryan Smith on February 1,2010 | 10:00 PM

    Interesting topic, too bad several reviews had to bring up race and money, typical and sad. The advance of science and medicine are more important.

    Posted by Doug on February 1,2010 | 10:01 PM

    Colleen, did you not read the whole article? they are considered 'immortal' b/c "they can grow indefinitely, be frozen for decades, divided into different batches and shared among scientists." As to what they plan to do with them, they already mentioned they were used to create a polio vaccine, to study effects of space, and probably a number of cell-relaed research. I hope the family gets something out of this, b/c their mother did a LOT for the rest of us, from the sound of it.

    Posted by PC on February 1,2010 | 10:01 PM

    THE AUTHOR OF THIS BOOK WILL BE TOURING SOON AND WILL APPEAR AT BARISTAS CAFE, NEW MARTINSVILLE WEST VIRGINIA ON FEBRUARY 27 , 2010 FOR MORE INFO GO TO baristascafe-pub.com or go to Rebecca Skloot’s facebook for tour info. GREAT BOOK

    Posted by Soren Shade on February 1,2010 | 10:01 PM

    I find this article most interesting and who would have that immortality gene reach started there, most befitting for this month.

    Posted by Donnell Clayton on February 1,2010 | 10:02 PM

    Very interesting story..........Good Work..... Nilanka Jayasooriya.

    Posted by Nilanka Jayasooriya on February 1,2010 | 10:02 PM

    I thought this article was quite facinating but also quite tragic in a way. If you think about it Henrietta was a poor woman dying of an uncurable disease. While we know nothing about her personality we do understand that she was a colored woman in a very racial society. It is probably a pretty good assumption that any cells from a colored woman at the time would not have generated a scientific interest at the time. it was also because of that fact that the scientist had to lable her cells with fictional name.I'm not sure it multi billions have been made on the sale of these cells but I do know that tremendous scientific value has resulted that has saved thousands of lives. The irony of this story is that Herrrietta's children feel that they should be entitled to royalties and riches. This is without a doubt the most dubious way to smear her memory.

    Posted by John on February 1,2010 | 10:03 PM

    Can you explain what you mean by "It consumed their lives in that way." Under the heading: How did they do that.

    Posted by Christopher Okonkwo-Onuigbo on February 1,2010 | 10:03 PM

    Fascinating story! A biology major, and I had never heard the story. Sure hope the Locks heirs will finally get what they justly deserve in the way of monetary compensation, cooperation and recognition. Would be unfortunate if this continues to be another disgraceful exploitation of people of color.

    Posted by Geneva Wiggins-Collins on February 1,2010 | 10:03 PM

    This story was great and it should go to all people that look down on people of color and know that we have always been there to assist in whatever way we could. Just think about this, this lady's cells are what they call immortal. These cells helped many researchers towards developing many medical cures over many, many years, and apparently still going strong today!

    I am extremely excited about this new knowledge and how it should make all of us feel, that we all have given something for the betterment of our society. That when you think that you can do without another race or other people then "BAM", you find out that someone amount us, (maybe someone that you would not even notmally speak to, or even shake their hand)has allowed you to walk, run, smile, hold your child or your wife or husband. What a joyful world we live in, where as the old saying goes,... "what is done in the darkness, eventually makes its way into the Light" In this case this Ladys darkness, has given not only light, but Life to many in a way she never dreamed possible!

    WAY TO GO, and I pray that the family received compensation for their Mothers DNA!

    Posted by Lennie on February 1,2010 | 10:03 PM

    WOW! This is absolutely fascinating. I'd like to read more about this! thanks.

    Posted by Adinda Nyotokusumo on February 1,2010 | 10:03 PM

    It is amazing and thanks to Rebecca Skloot for this. The world has come to know about immortal cells.

    Posted by Aminul Islam on February 1,2010 | 10:03 PM

    I think it is dishonest for scientists to take the cells of any living person for what ever reason without asking for permission from the patient. The fact that these cells benefitted society in general does not mean the end justifies the means. This would upset most people and to not reveal the source of the cells and give proper credit to the donor and the family is despicable! This proves that the scientific world care first about the research and much less about the patient.

    Posted by pz knox on February 1,2010 | 10:04 PM

    Very interesting and educational. I have never heard of this person or cell before. So many questions to be answered. Sure glad you help the family out, they deserved to be compensated. Job well done!! Keep up the good work.

    Posted by Connie P. on February 1,2010 | 10:04 PM

    but what about the cells?, how is it that they can live for so long?

    Posted by noah on February 1,2010 | 10:04 PM

    You'd think they'd at least say thank you.

    Posted by Ted Janes on February 1,2010 | 10:04 PM

    Fascinating! This is a story!

    Posted by Mike on February 1,2010 | 10:05 PM

    Nice story. It really tells on the GREAT WONDERS oF GOD'S CREATION. It is all in our hands how we take it... science... circumstances... values... money.

    Posted by Jeanne Labayen on February 1,2010 | 10:05 PM

    Does anyone think it odd that:

    -- People would start worry about how they could play the race card? What if the doctor was black? Why does color get your blood pressure up?

    -- The doctor "stole" the tissue? How many times have women gone in for a PAP Smear since the 50's? Have the doctors promised all those patients, black or white, that the samples would not be cloned or grown or used for anything other than the cancer test? Have they promised they would be distroyed?

    -- How is it that people always look for "compensation" for what has been done to their ancestors? I have had ancestors killed in wars, by cars, die of cancer, and I even had to carry my own dead son to the hospital years ago, at the doctor's request. Who has his cells? I do not deserve any "compensation" for that stuff.

    Folks, Get off the easy money (You Owe Me!) gravy train. The doctors don't owe you anything except the cells that were stolen and and a big apology. If you have a bad attitude about it, demand that the cells be distroyed! The doctors can harvest someone else's!

    Let's Do What's Right!

    Posted by Ken on February 1,2010 | 10:05 PM

    lol why on earth would someone tell their age in posts. well anyway this story will prolly end up as a rascist story classifying people by their color of their skin instead of their nationality. i will not be buying this book because it classifies her as a black woman . and not an american woman. article should read AMERICAN WOMAN'S IMMORTAL CELLS SAVES LIVES

    Posted by jeff on February 1,2010 | 10:05 PM

    This article is so interesting. I too wonder how many cells from different people are in a lab somewhere? If cells were taken from Henrietta they most likely were taken from others.

    Posted by F. Springer on February 1,2010 | 10:05 PM

    How beautiful...but sad! She lives, she dies....SHE LIVES!!!
    How awesome for science! Hoepfully she knows how much impact on science and medicine!

    Posted by Kelly on February 1,2010 | 10:06 PM

    Loved this piece, very interesting! I will be buying the book!

    Posted by Leslie on February 1,2010 | 10:06 PM

    As has been said, scientist DO know why HeLa cells divide forever, but the Yahoo! writer obviously did zero research.

    HeLa cells, like 90% of cancer cells, produce an enzyme called telomerase. Telomerase extends the telomeres at the end of their DNA, which allows them to divide indefinitely and live much longer.

    The purpose of telomeres, is to prevent a cell from mutating, becoming cancerous and taking over the body. If the cell can only divide a finite number of times, it will eventually die off before it becomes a tumor and starts to spread.

    Normal human cells are programmed to die when they run out of the telomeres that protect their DNA. This limit is believed to be the major reason we age and die. Finding a way to turn this on in normal human cells and being able to control mutations could potentially let people become immortal!

    Posted by Garrett G on February 1,2010 | 10:06 PM

    There are direct decendants of the Doctor that decided to take this woman's cell. Find them and make them pay. These people are living large. Black people have contributed a great deal to this country.

    I am disgusted by the doctor and the medical institution.

    There has to be someway this family can be compensated for what they have contributed to science and the many advances in medicine. The cells of a poor, working class black woman that have made many white people rich. The cells of a poor black woman that have educated so many white children, etc. etc. A poor black woman whose family, no doubt, would have never been able to benefit from the medical advances her cells made possible back in the 50's 60's or today, if they have no medical insurance.

    Posted by j king on February 1,2010 | 10:06 PM

    What about embryionic stem cells utilized from aborted babies......do the stem cell recepients pay the baby's mother a monetary sum? Does the abortion physician get a kickback from the sale of the fetal cells? Even though the contributions from this mother's (LeLa) tumor cells are phenomenal and indeed have saved lives and indeed have created large sums of money, so have cadavers to medical schools. Unfortunately there have been so many historical untruths or omission of the truth that frequently it is difficult to step back and evaluate these happenings from an honest and objective perspective.

    Posted by Patricia Setien on February 1,2010 | 10:06 PM

    People give samples of their cells to science often. I gave samples of my cancer cells for research. I don't require compensation for allowing my cells to save maybe - YOU. Today though, one has to sign papers acknowledging they know their cells will be sent all over the country, even abroad to help find cures. Research is expensive.We Americans are so money grasping it shames me. The cells are not gold, people. They are garbage to the person who has them. Thank God they are no longer a part of me. They can multiply forever outside of me for as long as they are useful. I didn't want them.But, maybe you would like the cancer so you could try to squeeze some money out of it. Good Luck.

    Posted by Anna Weldy on February 1,2010 | 10:07 PM

    it was indeed a science breakthrough! i just hope man wouldn't be interested in immortality using the HeLa cells...

    Posted by jael on February 1,2010 | 10:07 PM

    really enjoyed the the story i always say God is so amazing
    thanks Rebecca for sharing this with us whats the the name of the book?

    Posted by Brenda Smith on February 1,2010 | 10:07 PM

    Wow! I cant help but say thanks and God bless Ms Skloot. For taking the time to find out about Ms Lacks. The fact of the matter its doesnt matter if your black are white you wouldnt want no one 2 take anything of yours without your permission! The first thing you would do is take them to court.So to the Lacks family do what each one of us would do. Fight for whats right!

    Posted by Cleveland Rutledge on February 1,2010 | 10:07 PM

    An amazing story for so many reasons. Truly inlighting and inspirational to know life can spring from death. Hoping that Henrietta lacks gets her place in history and her family their due compensation. Science does have its place, but lets hope that ethics can keep pace.

    Posted by don on February 1,2010 | 10:07 PM

    An article about the cancer cells of Henrietta Lacks was was published many years ago. The article focused on the discovery that her HeLa cancer cells could travel airborne and infect other cancer cells being cultured in the lab. Apparently cancer cell cultures developed by various research institutions in the US and overseas were being exchanged for research purposes. It was noticed by one institution that the cell cultures received from other institutions had similar cell properties even though the cell cultures originated in different parts of the country or different parts of the world and in theory had never come together before. The HeLa cell properties were discovered to be common to these cultures. Somehow the HeLa cell properties had infiltrated the various cultures. Apparently HeLa cells that were shipped out of the US to other institutions for research and had unknowingly escaped airborne within the receiving lab thus infecting their other samples. Those labs inturn exchanged their cell samples with other labs and on and on. The airborne propergation of the HeLa cancer cell was not known at the research level prior to this time hence no provisions were in place to prevent the airborne propergation. It was the HeLa appearance in the seamingly unrelated cell cultures that would lead to the discovery that the HeLa cell could move through the air, and unknown to the research community, had infiltrared other cell cultures around the world for a long period of time.

    Posted by John Ferguson on February 1,2010 | 10:07 PM

    This story has its start in 1951. It took over 50 years for the truth to be told. This same thing happens every now and again. In 2060, someone will research the origins of some discovery in 2010, and then the truth will be told. Very few people are true legends (heroes) in their own time. Their contributions usually aren't recognized until years after their death. I found the acticle interesting and for once, found a book I would purchase. I'm glad Henrietta Lacks is now recieving the recognition she deserves.

    Posted by Dale P on February 1,2010 | 10:07 PM

    Remarkable story. Very interesting. Looking forward to reading the book. However, "Twenty-five yrs after Henrietta died, a scientist discovered that many cell cultures thought to be from other tissue types, including breast and prostate cells, were in fact HeLa cells", women don't have prostates--only men do.

    Posted by Deanna on February 1,2010 | 10:08 PM

    Very good piece of information regarding the importance of cell research. There is alot of benifits from this one persons cell properties. So to all those racist people out there that have a family/friend thats life has been saved by a Black Women. I just say, LOL. Funny how life turns its wheels. We are born equally, we just choose to live the way we live.

    Posted by Kevin on February 1,2010 | 10:08 PM

    That was an awesome piece! I am learning about cells in Science class, and this is something that just made me more interested in my studies!

    Posted by Jessica Jun on February 1,2010 | 10:08 PM

    Wow, fascinating! I am a high school student and I have always been very interested in medical research. This story just intrigues me even more. I definitely want to read this book, I have so many questions about her! Did her family ever get compensated? And what about her family members, do any of them have "immortal" cells?

    Posted by Sanela on February 1,2010 | 10:09 PM

    Excellent story! I am interested in reading the book. It is unfortunate, that Henrietta wasn't aware of what was being done! I am certain, in the interest of science she would have agreed. It is great that her family has this information. She will never be forgotten! It is ashame, she'll never know the great things she has done for others! Henrietta looks like a woman with a caring heart! Thank you Henrietta, and, that you Rebecca for your interest!

    Posted by Cindy on February 1,2010 | 10:09 PM

    So interesting i wrote a homework assignment for my third grade class on this!thank you

    Posted by jenna shayne on February 1,2010 | 10:09 PM

    If you have a sore throat the Dr. takes a swab sample of your tongue. He can then see what the culture shows in the way of a known infection. In many cases the Dr. takes cell samples so they know what they are dealing with. I would think she had no problem giving this sample, as it was likely part of her treatment. It seems half the people on this site are more concerned about someone being paid. I would like to know does any of her offspring have the same immortal cell ability? In any case she is not "alive" and is quite Dead. I would think the real Hero is the Doctor who knewd what he had found before discarding the sample. Nature is amazing!

    Posted by Ray on February 1,2010 | 10:09 PM

    surely if it werent for the cells of Ms. Henrietta Lacks - my grandmother would have surely died from Polio. The family really needs to be compensated and soon.

    Posted by Naylahknee Lah KNee on February 1,2010 | 10:09 PM

    It is not true that scientists make money on HeLa cells. Yes, the cells can be bought from some companies. But you basically pay money for the labor and materials involved: somebody should grow cells on special media, freeze them and pack them for shipping. To Colleen: Cells are immortal because they can multiply. Old cells die eventually, but the young cells keep growing and producing new ones. Speaking about money compensation: I would be very proud and happy if some part of me or my family will be living forever and helping people.

    Posted by Natalia_scientist on February 1,2010 | 10:10 PM

    Michael Creighton brought this whole thing up in one of his books: How unethical it is not to partially compensate the people from whom these cell lines are taken. Kind of like not paying a few royalties to a person who owns property that sits on the oil. I really miss reading Creighton's thoughtful books. He was way ahead of the curve.

    Posted by deborah on February 1,2010 | 10:10 PM

    i really like the story...they should have a justice to what the goverment or the people have done to them...i want to know more about the family and how they live in the community right now!its so interesting...i want to know more about the husband and the relatives that revolve on them

    Posted by khrisna jane casauran on February 1,2010 | 10:11 PM

    Great story I too would like to read the book, it would make a good movie. Funny how they changed the name to sound more white. And as for Bob even if they cut cells from your body they still belong to you, no one has a right to take what is yours and make money from it that would be stealing don't you think!

    Posted by Margaret on February 1,2010 | 10:11 PM

    This article really caught my attention and really like to know the whole story of it. Thanks to the scientists who really take time to study human anatomy esp cells or what we call the stem cells. I am too, willing to give my cells for a study just for the benefit of humanity.

    Posted by Ellen on February 1,2010 | 10:11 PM

    Henrietta's family should get something for all the money that the doctors, hospital and science made. If we all think back on how blacks were used for study. Remember cocaine? syphilis? They were used to see effects on humans and blacks were used. This family should be compensated. Xrays are property of a "hospital" too but this is experments that helped millions and millions were made.

    Posted by Diane Russo on February 1,2010 | 10:11 PM

    Wonderful story! Mind-boggling, really. It would make a great movie. Real-life is so much more fascinating than fiction! Thank you for a great piece.

    Posted by Stephanie on February 1,2010 | 10:12 PM

    i think that this is interesting and although great things came out of her cells, she should of had a say in what happens to her body and that they had no right to take anything from her with out her knowig either way that you look at it they stole from a women that just went to the hospital for help.

    Posted by michelle on February 1,2010 | 10:12 PM

    Most interesting thing I have learned about in the medical field!!I will try to find more about HeLa cells.

    Posted by jillian on February 1,2010 | 10:12 PM

    I don't think Henrietta would have asked for a penny if she had known she could have saved many lives. You said, her relatives didn't even know what a cell was. To them its not able saving lives its how much can we make off of Henrietta.

    Posted by julia on February 1,2010 | 10:13 PM

    This is a wonderful story and thanks to all the terrific scientist we have and to those in the past our hats are off to you.You unlock so many doors.

    Posted by Rose shaw on February 1,2010 | 10:13 PM

    They gave her the right pseudonym Helen Lack... Because ''Helen lacks'' proper compensation.

    Posted by Mark Bacon on February 1,2010 | 10:14 PM

    If anything, her family should be proud that she was in any way capable of helping science. I've lost someone to cancer, and any method that would help eradicate that disease or so many others is worth any sacrifice. I am definitely interested in reading the book. And I hope her family is proud of the contribution she may have made to eradicating any known diseases. Thank you to them for her contribution to science.

    Posted by G Beard on February 1,2010 | 10:14 PM

    Check this out from the library instead of BUYING IT if you're concerned with what you fund with your cash. Let's not further this exploitation; Consider sending the cash to the family instead of Skloot.

    I completely agree with William Thomas:

    "Rebecca Skloot is yet another in a long line of self-serving "experts" who have exploited Henrietta Lacks and her family. The "poor black" tobacco farmer, and her ignorant widower and children, being used as fodder for White Lady Skloot's artificial magnanimity is more than I can stomach right after lunch."

    Posted by Amy L on February 1,2010 | 10:15 PM

    Great story. Sounds like a good book.

    Posted by Arthur on February 1,2010 | 10:15 PM

    I hope Henrietta's daughter gets the answers she is looking for and I hope the family gets compensation since this was done without permission. Today, however, anyone going into the hospital for sugery needs to read the fine print and you will find that you give the hospital the right to experiment with any tissue they remove. They do not need to compensate you in anyway. But in the 1950's they did not have these release papers so the family should receive something.

    Posted by SteelCityWoman on February 1,2010 | 10:16 PM

    amazing work, Rebecca Skloot. I wish to see more of your work. Thanks Zielinski, you have done great to bring this story to us.

    Posted by gigi on February 1,2010 | 10:16 PM

    This story reminds me of the Tuskegee Project and is just another example of how Black life is undervalued in America. We absolutely owe so much to this woman and the legacy she unknowingly gave us. Her family should absolutely be compensated! She was not a donor...her cells were stolen without her knowledge! The theives didn't even feel ashamed about what they did to her to conceal her identity but that turned out to be the blessing. It took a nation of millions to hold us back and it still didn't work.

    Posted by Spagirl on February 1,2010 | 10:16 PM

    This is amazing I have never herd about this even during college years. There are many ethical and moral issues on regards to this case, However I am in health care and see people suffer on a daily basis. Can only imagine how many people it could help.

    Posted by Y. River on February 1,2010 | 10:16 PM

    i think this is a nice story, well done and understood! i have no problem with them taking my samples, i wont be needing them anymore when im gone, so i hope i can contribute to science to help others, its kinda of a way to live forever thru others to help others. :)

    Posted by Randy C on February 1,2010 | 10:16 PM

    5000 word excerpt in O (OPRAH)magazine from book...http://www.oprah.com/omagazine/Excerpt-From-The-Immortal-Life-of-Henrietta-Lacks_1

    Posted by robert on February 1,2010 | 10:17 PM

    Thank you for telling this article. Stories like this of people telling what needs to be told are always nice to hear. A big thank you to the family as well, for eventhough Mrs. Lack never knew what she did, through her millions of lives have been saved. If it had been me, I would've been so proud to have donated my cells. She truely is a life-saver, and I hope her family knows how thankful all those who recieved the polio vaccene, and others are to her and to them. I wonder if they will recieve any of the profit from the biography? If not, they should. All in all, a wonderful article. Thank you Henrietta.

    Posted by Michelle Johnsen on February 1,2010 | 10:17 PM

    I really enjoyed the article. And was very moved that once again a black person has improved lives across the world; but I think that it is very sad that a person died doing something to helped millions of people of multiple nationalities and did not get not recognized for the gift that was given(consented or not). However, the article was on time, considering on how so many people are hurting these days.Personally,knowing that someone gave of themself(consented or nor) to saved millions or the human race is just a miracle in itself.

    Posted by gertrude baker on February 1,2010 | 10:17 PM

    ...this is just a missing puzzle. Nice job done.

    Posted by O'Seun Olanrewaju on February 1,2010 | 10:17 PM

    great story! I wanted my cells to be studied

    Posted by bingo on February 1,2010 | 10:17 PM

    This was a fantastic piece. It is amazing what science can do. I do feel that the family should have gotten some money out of it. I hope the family can do something to get some of that money. It was wrong of the scientists to take the cells without the knowledge of the people envolved. That was selfish on their part.

    Posted by Sandra Libby on February 1,2010 | 10:17 PM

    I hope everybody think about cell owner and thanks for help us to get better life.

    Posted by rati on February 1,2010 | 10:17 PM

    nice story!...but i think it should not be a racial story, instead a enlightenment or learning to our medicine and science improvements and researches..the family of henrietta should have known about it.. thank you henrietta..

    Posted by ryan on February 1,2010 | 10:18 PM

    Bless Henrietta's soul. I bet you she is smiling and looking down and thanking science for the benefits her cells have done and will still be doing for mankind. It proves that cells are really important in researching for cures to diferent diseases. Thanks to her family who now understood the important of Henrietta's cells. ANd last but not least, Kudos to the scientists doing all those researches.

    Posted by Charie on February 1,2010 | 10:18 PM

    The Immortal Life of Henrietta Lacks By: Rebecca Skloot Crown Publishing Group 2010 about $14 or so at Barnes & Noble...or check your local bookstore. Also available on ebook

    Posted by Yael on February 1,2010 | 10:19 PM

    Wow. Does that mean that they are coming up with a way to make us immortal? Will they find a way to stop us from dying?

    Posted by Natalie on February 1,2010 | 10:19 PM

    Awesome piece!

    Posted by Elizabeth Gallardo on February 1,2010 | 10:19 PM

    Why does everyone have to be lawsuit-crazy? People just want a fast, easy buck. Sure the family should probably be rewarded something but really why is there a need to punish science? If you want money, go get a job and stop making everything so expensive by greed-driven lawsuits! Gross. Instead, this family should be enshrined in history books and their name should live on in a positive light in the name of scientific advancement.

    Posted by Harrison on February 1,2010 | 10:20 PM

    This is one of the most wonderful and powerful pieces I've read in a long time. These wonderful 'HeLa' cells are living "Life Gems". I am impressed by the persistance of the author. I am in awe of the history. I am grateful for a woman, whom at the time, had no idea what she would contribute to the world for years to come. For the family of Mrs. Henrietta Lacks, "march on 'til vict'ry is won". We owe a great deal to the living gem that continues to live on. I sent this article to my sisters, and to my friends. As for compensation for the family, I pray that the Human Spirit will prevail and do what is right and necessary to take care of the family. This is a story that will be echoed in the history books for years to come. It would be a shame that they cannot atleast send some royalties to a foundation created in Lacks' honor. In a world in which we pay millions for items we don't need, the most a foundation could bring is health care for the family. Something that their mother is truly and literally a part of. To the daughter, Deborah, thank you for giving the Author your trust and for being courageous in your spirit to allow her to help. I pray that everytime NASA sends a space shuttle to the moon...everytime polio has been cured and each time a medical mystery has been solved, you smile and know that as long as there is science, your mom will live forever. She was one "HeLa" of a woman. Many blessings, closure and peace to your family.

    Posted by makebster on February 1,2010 | 10:20 PM

    I loved hearing about Henrietta Lacks! She lacks recognition for the wonderful contribution her cells have been to anyone who has received the polo vaccine and any other help they have supplied in other research. I am a donor and will be honored should my contribution help cure anything and further anyone's life. I feel that every donor should be recognized and the surviving family informed about the discovery made due to their families donation. The Smithsonian has so many artifacts for us to admire, why can't we also have a plaque to inform us of the discovery and who helped with that discovery and not just the sceintist. I don't feel my family should receive money for my donation but a thank you and recognition for the importance of being a donor.

    Posted by DJ on February 1,2010 | 10:20 PM

    i come from other culture,i can't understand why you so interested in this story?

    Posted by toughman on February 1,2010 | 10:20 PM

    I found this to be very interesting, and am anxious to read more about it. Hopefully this will not turn into a race issue, nor will it become an economic issue for the family of the late Henrietta Lacks. Because of her cells, she has saved more lives than and ONE human being today. I find it simply amazing!!

    Posted by Latisha M. on February 1,2010 | 10:20 PM

    Excellent article. I want the book.

    Posted by Rick on February 1,2010 | 10:21 PM

    we all have views in life and we should understand what's not understandable.

    Posted by Jan Montana on February 1,2010 | 10:21 PM

    I have been a nurse for almost 13 yrs. It is always interesting to learn new and different information about people and their contribution to medicine. I had always heard of HeLa cells from anatomy/physiology, but had never heard how they came about, only what he have learned from them. That is very interesting! I cannot wait to read the book!

    Posted by Joy H. on February 1,2010 | 10:22 PM

    I really enjoyed the article and now I want the book!

    Posted by Candace on February 1,2010 | 10:22 PM

    I absolutely love this and I must buy the book. This is remarkable and truly a blessing in disguise for Mrs. Henrietta's family. I pray and have faith that they will get compensated for this amazing discovery. I hope that her descendants realize how incredible this is. Who knows maybe a grandchild might be inspired to become a scientist, biologist, etc. from learning how a part of their history helped the world....TRULY AMAZING AINT GOD GOOD.

    Posted by Ashley Nicholson on February 1,2010 | 10:22 PM

    what a most facinating article. Although there is one thing that I would like to comment on. The fact that her husband only had a third grade education does not make him ignorant. Just look at the picture of them he, looks like he's got it together to me. My father only had a sixth grade education and still knew alot about many things, it was a different time then children often did not go far in school because they were needed on the farm. Also her sons may not have thought much about the cells until money was involved so what? exactly what does that mean?. The minute that they started buying and selling those cells the family should have started being compensated, instead they were left to scrape by while the scientific community became wealthy! How unfortunate that people see this as a Black and White issue when it is really a matter of doing the right thing regardless of race.

    Posted by Mark C on February 1,2010 | 10:22 PM

    It's 2010, in 59 yrs this family should have already done something to stop living in poverty instead of now thinking oh wow lets cash in on Mom's old cells that did not die. Come on people, once you are dead your cells are either God's or if you were having tests due to illness as she was, they usually get discarded or used for scientific purposes. This way your loved ones do not die in vain if they can help save another life. My Mom had breast cancer, so now I guess i should track down her biopsy and see if anyone made any money off of it? Go get educations and jobs and leave Mom poor old cells alone! Oh and my Dad died from a massive heart attack, but before that he had a pigtail put in to help his aorta, all that they cut out of him, I need to know where it is and how much money was made from that to. My grandmother died back in the 50's wonder where they put her tests and cell tissue. Hell she died at 96, if her cells are still living then they really might be closer to immortal, maybe she could have lived to 835, like Noah. I need money, having a hard time, let me dig her up. Man could I ever live high on the hog instead trying to make my life better on my own dime. Think I will dig everyone up and go on a cell and tissue hunting trip. Besides that my cells belong to me and not my children or my grandchildren, they have their own cells!

    Posted by Karen on February 1,2010 | 10:23 PM

    Incredible story. I pray that her famiy is compensated.

    Posted by C. Ewuzie on February 1,2010 | 10:23 PM

    Fascinating story and well written - easy to read.

    Posted by Beverly on February 1,2010 | 10:23 PM

    This is another example of how scientists from the 20th century used afro-americans as genie pigs all for the name of science. The least they could've done was ask for permission, but it was ok at the time cause they were black. What's even worse the family was not even compensated. Every one involved in this research made a profit in some form or fashion. This is equivalent to some one stealing a patent for an invention, making profit from that invention and not sharing the proceeds. Sounds like the scientist had good intentions but ill tactics.

    Posted by Mark Crawford on February 1,2010 | 10:23 PM

    It is amazing how the writer of this artical made the Lacks son's out to only ask for money. The doctors and scientist who stole Mrs. Lacks cells are the GREEDY ONES HERE!!!!. They made Billons on her cells!!!

    Are the family going to be compensated for their mothers cells being used are that time and still!!!!.

    I first read about this story in the Oprah February 2010 magazine issued. I was surprized to see it here!!!.

    Posted by Karen on February 1,2010 | 10:23 PM

    I also would buy this book. This is very interesting and would make a great movie. I didn't know there was something called an immortal cell, sounds like something on the SyFy channel. Thanks, Rebecca.

    Posted by H. Hampton on February 1,2010 | 10:23 PM

    This is very interesting and I would love to read the book. Science is research and human being as well as animals are always being used for research with or without our permission. How many lives did this one woman saved? Thank you for your research!

    Posted by Yolanda on February 1,2010 | 10:23 PM

    nice story.... very interested.....:)

    Posted by red on February 1,2010 | 10:23 PM

    The story about Mrs. Lacks was told eloquently and poignantly by Ms. Harriet A. Washington in her (should be) seminal book, Medical Apartheid, published in 2006. The practice of using African-americans as guinea pigs has a long history, regardless of the spin given to Mrs. Lacks' "contribution". If you want to read about Mrs. Lacks, who lived at some point in Turner Station in Baltimore, Maryland, in a larger context, you should read Ms. Washington's book. You may want to read "The cells that would not die-the tissue of a Baltimore woman dead for 30 years haunts the medical laboratories, undoing years of research", Baltimore Sun, 28 Mar 1981; "The immortal cells of Henrietta Lacks", Reader's Digest, Sep 1986; "Her cells made her immortal", Baltimore Sun, 18 Mar 97. The last article, and a more current one (not cited), written perhaps four years ago, also express the sentiments of her family.

    Posted by Jan on February 1,2010 | 10:23 PM

    I am a research scientist and have personally used HeLa cells for my research. Henrietta's cells are immortalized because at some point, most likely in her adolescence, she acquired a Human Papillomavirus (HPV) infection. The virus remained in her cells which led to their immortalization, resulting in cervical cancer. As a lot of us know today we finally have an HPV vaccine and as an HPV researcher HeLa cells have provided a lot of vital information towards our understanding of HPV and cervical cancer, which has also led to HPV vaccine development. I could probably guarantee that almost every lab in the world has at least one vial of frozen HeLa cells which tells you how powerful these cells have been for research. However I know for a fact that the widespread use and availability of Henrietta's cells are an exception as the process of ethical approval to obtain human cells for research has gotten more and more difficult, as it very well should be. Although her cells have led to thousands of wonderful discoveries I do think scientists take these tools for granted. Its nice to see the name Henrietta instead of HeLa.

    Posted by Erin Isaacson on February 1,2010 | 10:24 PM

    THIS IS AWESOME!!!! :D

    Posted by sam on February 1,2010 | 10:24 PM

    The book "Next" is a must read for those interested in this topic. Just wondering, will Ms. Skloot give any profits to the now surviving HeLa family? Let's see. Black or White, and I happen to be a white woman scientist, having a daughter with a history of cancer who at this point is a survivor, I think the following: our cells are our property and the property of our heirs; universities have far too much involvement and control beyond scolastics (they pressure families and make huge amounts of money w/ the cell lines); drug cos are in the mix and promote risk; and the diseases that affect us all...and affect the few - are being stalled in helping us by profiteering and arrogance. I had to pay 4K to have my daughter's cells tested for a rare mutation OUT OF THIS COUNTRY! A local research university wanted her tumor to add her to a research project, presumably to "help others"...I said NO. If I had said "yes" as the ignorant, desperate mother that they played me for, I would not have been able to give my daughter the answer that she needed to live the life that she now has.

    Posted by R. Franks on February 1,2010 | 10:24 PM

    lovely way of telling the truth!

    Posted by anupama on February 1,2010 | 10:24 PM

    Thank you for this information. Here's hoping that good results will come from your hard work and belief that this story should be told.

    Posted by Hayes Gipson on February 1,2010 | 10:25 PM

    What's with this talk of compensation? The scientist took a part of her cancer, I doubt she would have objected to having some of the thing that was killing her out of her body. Did the doctor treat her unkindly otherwise? Was she tortured, or was the rest of her body used for experimentation? They took a few cancer cells, get over it people. Yes, it's horrible that she had to die of cervical cancer, but good lord, compensation? For what?

    Posted by Fanny on February 1,2010 | 10:25 PM

    NOW THEY WILL MAKE BILLION DOLLAR MOVIE

    Posted by mae mae on February 1,2010 | 10:25 PM

    Wow fascinating story.I really want to read this book! I wonder how mane cures have come from those cells? Her family should be compensated. I bet the big pharmaceutical comppanies have made billions off this womans cells. As for not saving her from cancer, It was the fifties-I don't think they had a treatment for cervical cancer then and who knows what stage she was at when the cancer was discovered.

    Posted by deeannek on February 1,2010 | 10:25 PM

    I believe that Mrs. Lack's sons were just plain greedy the way it was worded.

    Posted by Lil lisa on February 1,2010 | 10:25 PM

    Half a story enought to get people in a uproar do any of the norm know how many cells on the human body die and go on to regenerate each second of our lives this story very important but very miss leading for people who have no knowledge in human anatomy or even a clue that all human cells are the same regradless of color or creed. Thank you that is all i have to say about this.

    Posted by cheryl palmatier on February 1,2010 | 10:25 PM

    Big legal issue here. This family needs a very good lawyer - starting from the point of the Johns Hopkins' doctor taking a sample without the family's permission forward. I'm very sad for this woman and her family.

    Posted by cmb on February 1,2010 | 10:26 PM

    Yeah what a history, you guys should add this to every history books.

    Posted by abduloh on February 1,2010 | 10:26 PM

    i've read all the comments and i feel that if it was my mother i would like some kind of compensation for the simple fact back in the day scientest used the poor and uneducated people.she was black and WE ALL KNOWthey did little to save her.their main concern was to use her to better the white people.let's face it they used her as a ginnue pig the family deserves something.i'm not saying give them 100.000.000 one hundred million but something would be approiate.because if it were a white woman they would have dona everything they could to save her.and no i am not bkl but white

    Posted by nina stevens on February 1,2010 | 10:26 PM

    This is an amazing story. However, what the scientists did was unethical. They knew that they could get away from "stealing her cells" because she was black. Back in the 1950s something like this was just swept under the rug; no one would have ever believe that a black woman cells could have a major impact in medicine several years later. The scientists should have at least consulted with the family, informing them that we took some of your family's cells. The moral thing they could do now is atleast apologized to the family for stealing her cells and recompensate the family because if it wasn't for her cells many of the vaccination and other important discoveries would not have transpired. It's unsettling that we are now just hearing about this. People need to be informed of the great history lesson. Thank you for posting this article.

    Posted by angel24buffy on February 1,2010 | 10:27 PM

    I found this article very interesting. I want the book. Can you imagine the movie......WOW!

    Posted by Kandi Matamoros on February 1,2010 | 10:27 PM

    Medical Aparthied is a more relevant book to get. The experimentedon the woman without her permission. Anyone remember the Tuskegee experiments.

    Posted by Stokelife on February 1,2010 | 10:27 PM

    As these cells were taken from a cancerous cervical tumor caused by HIV virus and known to be carried on dust particals causing cross contamination I would be quite concerned with the outcome of their use. We should wonder what a so called immortal cell could do used in the polio vaccine an so many other medical research projects. We now have aids, widespread HIV,and many other dieases in young people that are incureable.

    Posted by D. Jochum on February 1,2010 | 10:27 PM

    This is an amazing story. However, what the scientists did was unethical. They knew that they could get away from "stealing her cells" because she was black. Back in the 1950s something like this was just swept under the rug; no one would have ever believe that a black woman cells could have a major impact in medicine several years later. The scientists should have at least consulted with the family, informing them that we took some of your family's cells. The moral thing they could do now is atleast apologized to the family for stealing her cells and recompensate the family because if it wasn't for her cells many of the vaccination and other important discoveries would not have transpired. It's unsettling that we are now just hearing about this. People need to be informed of the great history lesson. Thank you for posting this article.

    Posted by angel24buffy on February 1,2010 | 10:27 PM

    Medical Aparthied is a more relevant book to get. The experimentedon the woman without her permission. Anyone remember the Tuskegee experiments.

    Posted by Stokelife on February 1,2010 | 10:27 PM

    So it's ok for the medical industry to make billions trading immortal cells but it's not ok for the family in which immortal cells originates to be compensated in any way? Yes, Henrietta made a huge contribution to medical science but the medical industry is pocketing billions from it, which is ok too. I think at least a token financial payment is in order, particularly considering the financial struggles of Henrietta's family. They just need to hire a lawyer and I'm sure the industry will settle out of court.

    Posted by Mark on February 1,2010 | 10:28 PM

    Need to know more. I will be buying the book.

    Posted by Joan Ruffin on February 1,2010 | 10:29 PM

    I wonder if the author or publisher of this awesome story plans on sharing their profits with the family? Or you gonna stiff them like the researchers and developers did!

    Posted by Guy on February 1,2010 | 10:29 PM

    I'm a physician and a scientist. I briefly used HeLa cells in my work. I appreciate your thoughtful article.

    Posted by Scott on February 1,2010 | 10:29 PM

    After reading some of these comments I have to ask myself have we yet learned or acquired a sense of awareness or decency a woman and her family were wronged this was the 1950s lets be real back then it was just business white business if that had been a white womanor man their names would have been plastered all over the world but some poor black woman and her family were not thought twice of until they decided that they needed some more.Is rebecca biased or just stupid,why wouldnt the family be angry why shouldnt they recieve restitution if they were whit they sure as hell would wake up people something was stolen and weather it was for science or industry someone other than the big thieve should get paid I mean henrietta is gone what other restitution can they recieve.

    Posted by tony on February 1,2010 | 10:29 PM

    Alot of money is to be issued to the family, considering the cells were taken without permission and sold for millions (probably billions) of dollars. That is wrong and unethical, This is wrong and malicious.. You just don't take something from someone's without permision and make profit out of it ? I hope the family gets an amazing lawyer to sue the hell out of the scientist and it's organization for this malicious and unethical act.

    Posted by Senseless wrong story on February 1,2010 | 10:30 PM

    Utterly fascinating. Completely intriguing. I'm glad that the author had the courage to tell this story. May Henrietta Lacks rest in peace and may her family find solace AND the financial compensation that they are, most assuredly due, all these years later.

    Posted by JRF on February 1,2010 | 10:30 PM

    I will have to say I am very amazed and interested in a story that so many people respond in such a positive way. I have never seen so many positive responses EVER! Great job writing this piece.

    Posted by Darby Hilton on February 1,2010 | 10:30 PM

    Show the strength of the African-American blood line. The family should be compensated immensely for this. Only fair.

    Posted by Donald on February 1,2010 | 10:31 PM

    Great Article. I cannot wait to read the book. I feel her family should recieve some monetary compensation!

    Posted by Pam on February 1,2010 | 10:31 PM

    Why dos every thing have to be about money,Just think how many people it help,and will help with science,and msdicine,and I will read the book ,Thanks ms,Skloot

    Posted by R.C. on February 1,2010 | 10:32 PM

    Very, very interesting story. However, something tells me there is much more to this story and we will be reading about Henrietta Lacks and the HeLa cells again.

    Posted by Ginny on February 1,2010 | 10:32 PM

    did anyone stop to think that they may be giving cancer cells to other people in these vaccines, etc? esp is the cells can spread and contaminate through airborne pathways! that is scary to think that scientists use cancer cells for vaccines!

    Posted by Jeanette on February 1,2010 | 10:32 PM

    Nice piece of history. Too bad many of you only think of the race and money aspect!!

    Posted by Jim on February 1,2010 | 10:32 PM

    That was great what the Doc did he may have save alot of lives. But you know a close mouth don't get feed so the family should ask for a fare amount.

    Posted by Marie on February 1,2010 | 10:32 PM

    Thanks a lot Rebecca. Have learn & even used HeLa for research and yet now only i know the origins. Interested to know why HeLa is IMMORTAL. cancer cell lines finite culture for research would be juz <20 passage. hm...those scientist must hv taken quite A BIG LUMP of cells from her.

    Posted by weixuan on February 1,2010 | 10:33 PM

    I am so speechless,I cant wait to get the book and read it this is a amazing.

    Posted by Tonya Tucker on February 1,2010 | 10:33 PM

    It is so wonderful and we all should thank her... and all scientists for studiying medicine using Hela cells.specially thanks to that physician who dare to explore the unknown.....like dr. Alexzander Fleming did for discovery of penicillin.

    Posted by Ajay on February 1,2010 | 10:33 PM

    Amazing, yes- the family should have been compensated. This story I think reminds us that scientific inquiry both allows and requires us to be the moral agents that we are. Inspiring in a way. Definitely fascinating

    Posted by Bee on February 1,2010 | 10:34 PM

    good... and interesting unknown fact not only in the field of medicine... but in biology itself as a whole...

    Posted by michael on February 1,2010 | 10:34 PM

    The picture alone speaks volumes. Such a befitting story should be required reading in middle school science classes and above. Here is another example of the medi-sins created against African Americans but all is not lost because we now have the opportunity to grow in knowledge about the impact African Americans have contributed to medical science and industry. A must read. Let me know when the book is available.

    Posted by Dee on February 1,2010 | 10:34 PM

    This story sounds very interesting. Hopefully, Rebecca Skloot will donate most of the profits to the family. Finally they can begin to find their way out of poverty. I'm sure that's what the mother would have wanted. Although Mrs. Lanks didn't have a choice in any of this,everyone seems to be financially benefiting from her in the name of "Science".

    Posted by Yamiley Roy-James on February 1,2010 | 10:34 PM

    Is this for real and if it is, why haven't we heard of it before? Are you saying that the cells never DIED or that they were KEPT alive by the scientist?Or is this just to promote the BOOK?? Because it seems to be working. I don't have aproblem with that, just wanted to know...Is this serendity or....?

    Posted by Steve on February 1,2010 | 10:34 PM

    What a fantastic story. I look forward to reading the book. I believe the family deserves something for what their mother contributed and didn't even know it.

    Posted by C. Hatchett on February 1,2010 | 10:34 PM

    I won't waste my time reading a lot of this foolishness! The cells that belonged to the lady have saved SO many lives, I'd like to think the lady is happy and proud she could help the world so much. As for you racists, of all colors, shame on you! You money mongers the same! There are some people in this world that give and ask nothing in return! It was wrong to take without asking but I think the Lady would have gladly given! I know I would have! Some of you make me sick that we are of the same species!

    Posted by Don Lippincott on February 1,2010 | 10:34 PM

    Great article! The book and story sound very interesting. It's also interesting that the brother didn't care until he heard about the $$$. Not to sound racist here but one was already homeless. Money can only help or hinder this family and I'm thinkin' it's the latter.

    Posted by Jay on February 1,2010 | 10:35 PM

    The article is interesting but it makes me ask, are most people's cells so-called "immortal" and her cells were only available to science because they were taken without consent? ...or was it because it the cells were cancerous? I totally appreciate what contribution, she as a black woman could give us - but really regardless of who she was -the "gift" was taken, not given and she didn't even know, right?

    Posted by T M on February 1,2010 | 10:35 PM

    Wow!...this article is very amazing!...

    Posted by MARY JEAN P. MATILDO on February 1,2010 | 10:35 PM

    This was such a wonderful and interesting article, I enjoyed it so much. I, like so many others, am wondering if the family received any compensation for their wife, mother, sister, they really deserve it. She was a beautiful lady. I am so going to go and buy the book. It should be on the best sellers list somewhere.

    Posted by G. Thomas on February 1,2010 | 10:36 PM

    WOW great writing I cant wait to read the book im sorry for the people in Laredo TX their last and only book store is closing :(

    Posted by Monica R. on February 1,2010 | 10:36 PM

    This is really amazing story i wanted to read...... I'll will find this book.... AMAZING!!!!!!!!...

    Posted by Aldrin M. Tacna on February 1,2010 | 10:36 PM

    Well I say its great. I'm sure Henrietta doesn't mind her cells remaining alive to better mankind. I mean how many women can say their cells out lived them or their fashion sence?....LOL.... However if there are books and movies involved; I think the family should recieve money off of them. That is only the right thing to do. ( By the way I'm her granddaughter) JUST KIDDING....lol I say LIVE ON cells of Henrietta! VIVA los cells de Henrietta!

    Posted by Kandi Matamoros on February 1,2010 | 10:36 PM

    This was a great article. It is sad however, to know that any of us could have the same thing happen to ourselves or our families. We are not subjects to be used as doctors see fit. We are people and we must fight daily for our rigts and freedoms.

    Posted by Meshell McRell on February 1,2010 | 10:37 PM

    This is very interesting. It makes you wonder what other genetic anomalies are out there waiting to be discovered or revealed to public eyes. Though the genetic and other medicinal work is amazing it is still wrong that her cells were "stolen" and i hope that the family will be compensated in some way.

    Posted by runiac on February 1,2010 | 10:37 PM

    :) The best article 1 ever read.. Can't wait for the book. Thank you Rebecca Skloot & may God blessed Lacks family.

    Posted by Geffry Joshua on February 1,2010 | 10:37 PM

    Fascinating. Great to share with children. The study of science is taking place right now in front of you. I particularly got a kick out of the,....."can't we figure out a way to sue this guy" comments. There we all are then, on top of the dung pile.

    Posted by P Mc Carthy on February 1,2010 | 10:38 PM

    In this day and age, I would think the family should have medical coverage & prescription coverage, in lieu of their mom's indirect but totally her, contribution to the medical field. Whether she knew or not, I would think the medical CREED would have an affect.

    Posted by Karen McKahan on February 1,2010 | 10:38 PM

    I would like verry much to read the book

    Posted by arthur on February 1,2010 | 10:38 PM

    Great story and God bless for Henrietta's family!

    Posted by cora on February 1,2010 | 10:38 PM

    This story is incredible and there should be a documentary film about this. for the family of the Lacks, thank you

    Posted by dante calantuan on February 1,2010 | 10:38 PM

    This revelation is ecstatic and I thank God for allowing this to surface after so many years.Thanks Rebecca Skloot for your presistance.

    Posted by Nan Piggott on February 1,2010 | 10:38 PM

    What if we're meant to be immortal! This is such an amazing story. Would make a great movie.

    Posted by lili dauphin on February 1,2010 | 10:38 PM

    While I do not condone the "stealing" of anything from anybody, by anybody, why is the focus on compensation rather than the millions of lives saved by her cells?

    Can we not just thank God for working his miracles thru us, in this case, thru her?

    Posted by Mark on February 1,2010 | 10:39 PM

    Thanks for putting this out there and making this accessible. Will get the book for sure!

    Posted by Charmayne N on February 1,2010 | 10:39 PM

    If even a single cent of monetary profit is gained from the use of cells harvested from individuals, those individuals, and/or their heirs, should share in these profits.

    Posted by Lewis Davis on February 1,2010 | 10:40 PM

    This is an amazing story. Thanks for sharing it. One never ceased to be amazed by perhaps thousands of untold true stories such as this. Great reseach! Im looking forward for the book.

    Posted by Horacio Rosario on February 1,2010 | 10:40 PM

    she was a participent,,if possabl she would have had the benefits of the discoveries from the research doctors medical expertise . The role played by the research doctors supperseed her passive contribution of the right genetic cells at the right time. Dont be stingy Henrietta, some one else would have done the same thing for you if given a chance to contribute their cells ,,,For one brief moment in time her link in the chang of life was uniquetley important,,You give a little you receive a little..Would not the chance of benefitting been the deciding factor???She was a medicaly beneing participant,she was not the developer of the medical benefits. You take a chance; some times u win , some times u loose; but you do your part to keep the game moving,,.Without the doctors medical expertise she would still be a 'gonner'. What dose she want??'eggs in her bear'?

    Posted by jos blanda, rochester ny on February 1,2010 | 10:40 PM

    Well-written piece. I am not a big reader but I appreciated this one. It's history and science in a nutshell.

    Posted by Nikki Lawson on February 1,2010 | 10:40 PM

    Interesting story and twist on science!!!!

    Posted by Maria Welborne on February 1,2010 | 10:40 PM

    It is important to remember that we are NOT our cells. When our soul goes back to God we take NOTHING with us. Since we didn't design our bodies, we do not own them, we are only responsible for them until we die.

    Posted by Jewel on February 1,2010 | 10:40 PM

    No matter what cell, whoes cell...it all makes sense. God works in mysterious ways. I am very impressed and in awe of this story. So many black people were confined let alone denied of a right to life and I can not imagine what this family felt when they came to hear the news. Better them and their generation(s) than mine. Whatever it takes to discover and to find a cure is what science is all about. Thanks to all scientists whom have heart and patience to reveal science in its unknown being. I am 100% amazed with this story as should everyone...I love this site.

    Posted by Angela Fisher on February 1,2010 | 10:40 PM

    I'm African American, male and wanting to practice medicine someday. This story is soo tragic on so many levels...Tuskegee Experiment? Makes me really think about HIV in the African American population.

    Posted by George Jamison on February 1,2010 | 10:40 PM

    ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
    Hello Rebecca Skloot, what a moving piece of great information. I feel every person should be aware of any human testing. Although, I realize that this type of behavior went on during the this time and earlier with merican black people, such an inhuman act. Yes, great for science and humans. I truley feel that Henritta's entire family should be compensated for the cruel behavior of that was brought to her. Thanks so much for this sincere sharing of information.
    ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

    Posted by Kyra Jenkins on February 1,2010 | 10:40 PM

    This is Amazing

    Posted by pricess on February 1,2010 | 10:40 PM

    This is a great story; looking forward to the book or even a movie.

    Posted by N. Jefferson on February 1,2010 | 10:42 PM

    I enjoyed this bit of the story. I learned about this about 2 years ago when I was taking a Biology class. I am 50 and going back to school. If I am not mistaken, I do not think there was anything mentioned about the person being black. But the cells were discussed and her name was mentioned. I am interested in the book. I really hope the family was given the money they deserved for the use of their mother's cells.

    Posted by Michelle Robinson on February 1,2010 | 10:42 PM

    Great piece of information. Makes me wanna write a song about immortal cells lol!!!

    Posted by tawn on February 1,2010 | 10:42 PM

    This is definately a facinating story. There was a lot of learning points in it as well.
    It was very informative but also left you asking enough questions to make you want to continue on in to the book its self.
    In regaurd to her family, I to think that they should be paid royalties on the money that is and has been generated from their mother's unwhitting but fortunate participation in this bit of valuable medical history. Her whole family should be set for life.
    The problem is that some blood thirsty attorney will end up with 1/3rd of the family's money. (The pun was intended)

    Rich

    Posted by Rich on February 1,2010 | 10:42 PM

    the only way to knw if the family got the MONEY is to get the book. even if the fam. got 10% of the money they mite b the richs people in the world

    Posted by Forrest on February 1,2010 | 10:42 PM

    if the hela cells are responsible for a polio vaccine, could it be possible that henriettas family has already been compensated? did any lack offspring have polio? what is that worth? who wants to sue a scientist that comes up with a polio vaccine? what if henrietta would have wanted to be part of a cure? looks like there is alot to this story, and looks to me like it has come full circle.

    Posted by keva on February 1,2010 | 10:42 PM

    my goodness what a great story. i want to learn more and can't wait till i can read the book. and i also wish good rewards for her family. they deserve it.

    Posted by pam gilliam on February 1,2010 | 10:44 PM

    Great story. Cant wait to get the book and read more about these immortal HeLa cells..Thanks Henrietta. Truely amazing.

    Posted by Ruth on February 1,2010 | 10:44 PM

    Isn't this the case where you are supposed to agree (without pressure) to donate your body(or parts of it) to science or to help others.

    If your body parts (or cells) were procured (not donated) with or without your knowledge and used in such a way that jumpstarts a multi-billion dollar industry, shouldn't you or your family be entitled to some share (residuals)? Or at least science and the companies recognize the contribution of HeLa cells to their work and agree on some form of compensation for the immediate family.

    Its sad that while HeLa cells were used to further develop medicines (that may cost a lot) the family of the person where the cells came from are not doing well. This is not to say that all of the family members should be getting support for life but to get acknowledgement of the contribution of their family member to health care. Maybe support for her sons and daughters.

    Posted by Howard on February 1,2010 | 10:44 PM

    Regardless of the intended medical benefits,just like with any other medical procedure or Organ donation CONSENT should be obtained.

    Posted by Robbin Hester on February 1,2010 | 10:44 PM

    This is a very interesting story! I cannot wait to read the book. I'd like to know more about the family and how they endured through this ordeal. The most shocking is some else selling the cells for money and the family getting none. Sad but true.

    Posted by Teri Ford on February 1,2010 | 10:44 PM

    ... wow, that's amazing... ^^

    Posted by rey on February 1,2010 | 10:45 PM

    This is an awesome story! I love her picture she looks beautiful. Her cells have shaped science. I will be looking for this book.

    Posted by JH on February 1,2010 | 10:45 PM

    dear god this is amazing with good science life can be immortal

    Posted by barbara howell on February 1,2010 | 10:45 PM

    As an African-American woman, I am literally blown away by how dismissive the author appears when referring to the reaction of Herietta's sons. So just because they didn't take an altruistic position and say "Well, don't worry about the fact that the cells of our mother spawned a multi-billion dollar industry. Forget the fact that her tissue was taken without her knowledge or consent and her family can't even afford access to the heathcare innovations made possible by the tissue. We're just glad we could help." Am I the only one who is reminded of the Tuskeegee Experiment when reading about this? Growing up, my granbdmother's generation which was the same as Henrietta's was very distrustful. The longer I live and the more stories like this come to light, the more I realize they had a reason to be cautious.

    Posted by Kim on February 1,2010 | 10:46 PM

    What an amazing story. It is history, medical breakthroughs, mystery, humanizing, and lovingly written by Rebecca Skloot. I am excited to read the book and hopefully be able to know the real lady behind all this controversy. She has left her legacy without even knowing about it, greed, yes by the ones who did this, but what a legend of information they have given to us in the field of medicine, and done without the FDA, I hope, who blocks everything besides big Pharma and much of that is bad meds and misinformation. I am so thankful that this has been revealed to all Americans who want to know why, like stem cell research, cannot be used to help those who truly need it. I may not see the answers in my lifetime, but this is truly exciting news for us. I would love to know the real lady who did not know what she has done for us with her cells. May her soul rest in peace and may we find out real answers to health mysteries. I will be looking forward to reading the complete book on HeLa. Her relatives do deserve monetary compensation from the ones who took her cells without permission and I do think they should have to pay for using her cells all these years. Thank you for your gutsy reporting on this wonderful article... I can't wait to read your book.. Thank you.

    Posted by Mary Macomber on February 1,2010 | 10:46 PM

    I will have to read the book to make an educated assumption. As for the HeLa cells, without this woman's unknowing contribution, she has unknowingly helped millions of others.
    I do hope that the author will be giving some of the proceeds from this book to the family. Espeically the daughter that helped her find more information and more family members.
    There are a few other questions that cross my mind at the moment but I will have to read the book before I can ask these questions because some of the answers may be in there.

    Posted by Betty McCullough on February 1,2010 | 10:46 PM

    Could someone do a little research on how these cells had came to mutate into Immortal cells... I would do it myself but I don't have the resources to do it...

    But my point to this is, if there was a way in which these cells mutated into something Immortal, and I don't know if it's unique about the cells differentiating traits into other cells through the air... but that may lead to traced mutation... Idk, it's a good opening for an invention... =P

    Posted by Justice on February 1,2010 | 10:47 PM

    It seems to me that if money is being made on her cells, her family should certainly be given some of that money, particularly since they need it very much, and there was never informed consent in this case. Peace,
    Shira

    Posted by Shira Destinie Jones on February 1,2010 | 10:47 PM

    I have a dumb idea about ways we can help out to honor her spirit and contribute something to her family. How about requesting the publisher to donate a little portion of the book profit to set a non-profit foundation to honor her, also support her family, and cancer medical research?

    Posted by P Hsu on February 1,2010 | 10:47 PM

    This is an amazing story of Henrietta Lacks " immortal cells ( Hela cells ), that change science and without it we would not be where we are now. i think her family should be compasated for life, that way they are given back for what was gained through her.

    Posted by Deborah on February 1,2010 | 10:47 PM

    What do they mean by "her cells never died".

    The author should explain the normal life cycle of tumor cells, which I don't feel like researching.

    Are the cells from her tumor different than other human cells? If so, why?

    Posted by Ren on February 1,2010 | 10:47 PM

    If they weren't compensated shame on us! Even an endowment for the future kids education would mean alot.

    Posted by Rich carlson on February 1,2010 | 10:47 PM

    "The cells are not "immortal" per se, they are just capable of surviving the "rough" conditions of the period in which they were harvested. They culture/growth of cells at the time was not as advanced or as promising when attempted at the time because the methods weren't as refined." I'm quoting my Grandfather with those comments, at 98 I think he has a rather wide experience with modern medicine having recieved his doctorates at 26, 76 years of theoretical and applied research in medicine (and engineering, he recieved his second Masters at 34).
    "Also, it has been in my experience that most cells can become airborne (we constantly slough off skin cells all day long, the chances of becoming "infected" with with cancer are", I've just been told, "slim and a "snowballs chance in hell". They are not (cancer cells) a contagious disease to be passed from individual to individual" (with very few exceptions I must interject here, cervical cancer ((some form, mine is not a medical degree)) transmitted to a woman from a man through intercourse is actually caused by a virus so it is not neccesary to correct me here I'm not too "ignorant" thank you.).
    Also the answer to whether or not they recieved funds from the harvesting of the cells and subsequent research is a matter for the courts, it was not common practice in those days to pay people for samples taken from them when used for diagnosis, now that is not to say the original intention was or was not for diagnosis, we have to give the doctor the benifit of doubt and the plausable idea that perhaps after the samples were taken the idea was posed to try and culture them in the hopes they would be viable as so many others at the time had not been so.
    Mrs. Skloot, an interesting story, thank you.

    Posted by Glenn on February 1,2010 | 10:47 PM

    Am I missing something? This woman had a piece of her essence stolen and distributed to save lives....her name not even recoginized....her family living on the streets while many strangers have profited!! Another shining example of Black people being exploited with no compensation or the least amount of respect.....SOS

    Posted by disturbed on February 1,2010 | 10:47 PM

    It great story never told, more should be revealed and eventually truth told concerning the mystery of this cells.

    Posted by S.ndonye on February 1,2010 | 10:47 PM

    For the person who claims to have been in sales for a period of time. (Three decades according to you.) I am astonished that you have the nerve to be condesending yourself as if three decades has taught you everything. You said you sized up your customers before choosing a level of speeh. What if you were wrong at least 1/4 of the time? I have no doubt that you think that a person with a lower level of education is in need of your a "dumbing down" way of communication. He may be a bright man with little education and a little honest expination might have done the trick. As for the welrare comment "stick it". This family has been robbed of what could have been a different life. Then they may have been educated enough to dumb down speech to you had they been rightfully or even fairly compensated. If there was nothing wrong with what the doctor did or how he himself profited, why did he not come forth and contact the family, starting with Henrietta? Look, this country has been built on the efforts of people who wanted a better life for themselves and their families. You lie, if you claim you would not come forth to claim your share of what could be billions. This is not an issue of black and white, but rather right and wrong. This family was wronged and they deserve compensation. There sould be no shame on the familys behalf, for wanting and even expecting, compensation. After all Henrietta died and through that, thousands have lived because of her unwitting contribution to science. That in itself deserves some recognition. Henriettas whole name was not even used durring the long period of research, thereby avoiding the recognition she so richly deserves. I am sure the family of the doctor who took her cells lived fairly well, or better. Why shouldn't hers? In this persons opinion (and many others I might add.) They deserv a portion of the profits because her cells were STOLEN from her and her family.

    Posted by Dee on February 1,2010 | 10:47 PM

    FAIR SHARE, AS WE ALL BENNIFIT FROM ONE FAMILIES TRAGIDY.
    RESEACHERS SHOULD COMPINSATE THE FAMILY FOR WHAT WAS TAKEN WITHOUT PERMISSION.

    Posted by RICHARD on February 1,2010 | 10:48 PM

    Well if that photo is of M/M Lacks. They sure are well dressed and a beautiful couple for being uneducated crop farmers from the south. She is even wearing fur !

    Posted by Mary S on February 1,2010 | 10:48 PM

    Its is amazing to read such selfish views on this subject.

    America is is serious trouble......if this education system is producing such sad beliefs.

    The truth is a s follows:

    "Just guess, Think you can put a number on how many lives the HeLa cell alone has saved?"

    Posted by Dr.obert Sutherland on February 1,2010 | 10:48 PM

    There's nothing else in the world quite like African mitochondrial (maternal) DNA!

    Posted by Dawne Richardson on February 1,2010 | 10:48 PM

    This is a instersting story. But to lighten up on some of the harsh things said about greed. I am Sick of a lot of things what Lab wants my Cells.

    Posted by David on February 1,2010 | 10:48 PM

    im so amaze about the true story what is really in the cell?
    i dont know anything about medicine but most of my father relatives are medicine,think they know about these? and also i have tumor but i dont think it seriously.i feel so sad to the family why all these years cell culture sciencetist didnt give them what the family of HL deserve

    Posted by mae ann khoori on February 1,2010 | 10:49 PM

    And then someone will write a fiction book about a clone human derived from these cells and call it a HeLa monster.

    (The Gila Monster is a lizard)

    I think her relatives would be due royalties on such a book for using her "name" in such a non-scientific manner without their permission, so let's keep a watch for them. While parody is protected by the First Amendment, the woman was not a monster.

    Posted by Tony Smit on February 1,2010 | 10:49 PM

    That is truly incredible. Her family deserves compensation if they haven't been compensated yet. Would that qualify her for sainthood, or was this gods way of ensuring they eventually paid her family for this? Hmmm....

    Posted by Sue B on February 1,2010 | 10:49 PM

    Wow C. Frazier, spoken like a true American. Who cares about the beneficial scientific impact, can the family sue?! THAT is the attitude that is ruining America.

    Posted by Casey on February 1,2010 | 10:49 PM

    If immortal cells don't mean immortal life I don't care.

    Posted by Richard on February 1,2010 | 10:49 PM

    Heart-felt analysis by Rebecca Skloot. I want to BUY this book!!!

    Posted by Mulia Rahhim on February 1,2010 | 10:49 PM

    I'll be dog gone.

    Posted by larry moore on February 1,2010 | 10:49 PM

    I almost forgot...the families are more than deserving to receive bucoo bucks for all that has taken place/discovered. Whatevere the color of their skin they are deserving to receive compensation for the use of the cells when they were not even aware that it had been taking place for years and years. They have the rigtht to be compensated because the government was funding the money for scientists to use Ms. Lacks cells and deliberately ignored to tell let alone ask the families. What a shame our country has become after all these yrs. One would think segregation/desegregation was a horrific time in the colored peoples lives but this here is just an unbelievable crying shame to the present generations. God bless the families.

    Posted by Angela Fisher on February 1,2010 | 10:49 PM

    This is a very interesting story. Her immediate family should be compensated. Her life was put here for a reason and her cells were left here for a reason.I also would like to read the book. The journalist did an awsome job of getting this information to a book.

    Posted by kenneth on February 1,2010 | 10:49 PM

    This is a very fastcinating story we have to be very thank this full for this lady cell and what science was able to achive,but moral taken her cell without her famlily promission was wrong,those who has profit of this ordeal should rightfully compensate her famly.

    Posted by Ashley Bannister on February 1,2010 | 10:50 PM

    Many of the comments on this article are ridiculous.

    First, as many have stated, the biopsy was taken in the 1950s. The medical regulations we have today were not in place then, hence the use of the cells without permission. This would not happen today, so no need to worry about your cells being used without permission (doctors/researchers need your consent). Using human samples/specimens is strictly regulated (in the US atleast) and many, many hours go into receiving approval.

    Second, the reason the researchers didn't provide her name originally was for privacy reasons, not because she black. Today researchers usually don't know the names of the samples they receive. This is so you can't google them and/or contact them. Patient info is kept private to prevent family members from being called and thinking that their wife is being kept in a lab as a lab animal years after you laid her to rest. It also prevents people from thinking they are owed monetary reward. Millions of people have donated cells to science just as Henrietta did, everyone's contribution is the same. Patients can't control what experiment their cells are destined for after they have been collected.

    Third, the doctor and/or researchers didn't harvest Henrietta's cells with the intention of selling them. They cultured the cells and realized they could be an excellent research tool. These cells rapidly divide so they can easily be grown and passed from researcher to researcher. Eventually it was realized that the cells could be frozen and sold. There is a not a single person who has made billions off of Henrietta, but instead the cell culture industry is a multi-billion dollar industry. There are thousands of cell lines, not just HeLas.

    Posted by Scientist on February 1,2010 | 10:50 PM

    Please please people get ahold of your selfs you all sound like a bunch people looking for the fountain of youth.In the next life you will get your immortality, wether it will be a pleasant one or a painful one. Try to remember how you behave here on this planet, and how you treat all your fellow human beings, because this will have a lot to do with where you will spend your desired immortality.

    Posted by Rain on February 1,2010 | 10:50 PM

    Great artacle. I would like to read the book too!

    Posted by Deborah Lee Brown on February 1,2010 | 10:50 PM

    well this is a very nice article.the word immortal made it interesting,

    Posted by rhien13 on February 1,2010 | 10:50 PM

    This is really interesting story.. I'd love to read this book soon....

    Posted by Aldrin M. Tacna on February 1,2010 | 10:50 PM

    Is it true?

    Posted by blaze on February 1,2010 | 10:51 PM

    Thanks for writing this beautiful article .I loved it ,I can't wait to buy the book.

    Posted by irene Asadipour on February 1,2010 | 10:51 PM

    Reading positive things in the news like this makes me LOVE my major! I am currently a college student with a major in Biology and I have a test in the morning about this very topic. While I was "taking my break" from studying I came across this article and I found it very informative, interesing, and entertaining! It was a good excuse to take a break. It is so fascinating how the simplest form of life can help save many lifes!

    Posted by T. Speight on February 1,2010 | 10:51 PM

    This was good work on your behalf, congratulations and thank you!

    Posted by Pierre Murguia on February 1,2010 | 10:51 PM

    Thank you Henrietta Lacks and family. I think the world owes you and should pay your family royalties and put your kids, kids though schooling. Pease out!

    Posted by Jerry on February 1,2010 | 10:51 PM

    Good piece. I'm on my way to Powell Bookstore now.

    Posted by Melanie on February 1,2010 | 10:51 PM

    Interesting and very informative topic...thus it is regretful to those who made profit/sell/experimented the cells, without giving knowledge to the family because they are poor or black people?

    Posted by virnalize chua on February 1,2010 | 10:51 PM

    thts a great article.wow!

    Posted by Dr.nazneen on February 1,2010 | 10:52 PM

    God Bless "Henrietta Lacks" & family. My prayers go out to all exploited people. I believe the subject is about THEFT & human rights) for Henrietta. If any human cells, body parts are relinquished voluntarily-donor beware! Why was Henrietta's tissue stolen? Profits earned go to scientists/doctors/publishers and them only without dispute. (The tissue was stolen with diabolical motive.) Companies produce false information about water...that is supposed to be good for you, but is poisoned. (Movie-Erin Brachovich) Profit not gained through moral means are immoral. Also, Hopkins hospital-came back to this family for further uncompensated(dangerous?)research. Studies are financed by Gov't grants, billions still earned by Pharma-medical companies.(American $$$.) Don't give me that BULL about sciencetist doing something altruistic--for mankind. This crime was perpetrated in 5o's so most Blacks weren't treated in White hospitals! Treatment was given at hospitals that accepted Blacks only-segregation. Did Henrietta receive proper medical attention...NO!. Most White scientists,etc. in 1950, didn't consider Blacks equal, so she & her family were used in unpaid-scientific experiments. Proceeds for books/movies/etc, should go to the moral "owner" of the cells. This family needs a good law firm. The moral owners of HELA cells are Henrietta's family,her cells were stolen, not donated & are still being sold. Historically, theives benefit using inhumane techniques in the name of science. Hopefully this diatribe, will stir awareness that these tecniques are used in hospitals today. (Organ Donors/tissue) Hospitalized Americans should demand all tissues be returned to owner. (No free samples) If we want to sell tissue I'm sure there's a buyer. If we decide not to sell...it's our choice. Medicine/science then as now, builds wealthy empires on the downtrodden backs people. Moral conscience, profit & restitution is the question. Angeli Sherley-Black Female in America.

    Posted by Angeli on February 1,2010 | 10:53 PM

    Thank you Rebecca. You have opened our eyes to a hidden truth. I am wonderng how many more stories like this are left burried in some museum somewhere? Black people have contibuted so much to the advancement of the human race,
    but are not given the recognition they deserve. Is it due to fear or the thought that one(human race) is better than the other and anything to prove otherwise must be erased? The younger generaton must read this book so our legacy can be preserved through the ages. THIS IS POWERFUL!!!

    Posted by N White on February 1,2010 | 10:53 PM

    Very interesting story!...

    The good thing is that she has helped saving millions of life. At the same time it's too sad and ironic that some of their relative have been living in such a poorness, while this people have been making such a lot of money for years and no caring about them.

    The scientific practically stole her cell's without her permission, as I understand! Can anyone think what this scientist could have done to may other people?

    Now, on the scientist track, how could these cells never die and continue multiplying? Every life "has" to die.

    Why can these not be good yet for HIV and other lethal diseases?

    Anyhow, the story is really interesting and I hope the family is rewarded now!

    Posted by Joe on February 1,2010 | 10:53 PM

    This i must say has been a very interesting read. This would have seriously tickle my brain. Is it to say that people who have uncommon diseases are likely to have a similar tissue response. I am not even scientifically inclined and my brain is running with theories. This was a real interesting story and the first i can call hearing of Henrietta Lack. I really hope to hear more. Gone for a google search

    Posted by Kadri-Dale Campbell on February 1,2010 | 10:53 PM

    Science has always fascinated me and now you have only made my curiousity even greater. Thank you for being interested in something that has opened all of our eyes.

    Posted by vicki kimbrel on February 1,2010 | 10:53 PM

    This is a Wow!!! story, I will look for this book!

    Posted by Juan Alvarado on February 1,2010 | 10:53 PM

    Great Story... Wow I want to know more

    Posted by Renee M on February 1,2010 | 10:53 PM

    What a wonderful story, when we heared a story we intend to find out what is the story about, well now i know, not only Obama is the only black person that contribute to black people story. thanks HENRIETTA LACK, REST IN PEACE.

    Posted by MOUHAMMED ADAMOU on February 1,2010 | 10:54 PM

    I have the same questions as Julie Hearn. What was it about her cells that cured polio? If that is true, why are we just hearing about it now? Is the author saying that the vaccination was made using the HELA cells?

    What is it about her cells that they are referred to as "immortal?"

    How do they still have them, are the scientists able to make exact replications of the cells? I too am going to buy this book. I just hope it answers my questions, I want to learn more about this subject.

    Of course if these cells made millions of dollars the family should have been compensated. That's a no-brainer.

    Posted by Debbie on February 1,2010 | 10:54 PM

    Oddly enough..I just read about this last night on Ripley's Believe it or Not..I liked their version of the story better..

    http://www.ripleys.com/blog/henrietta-lacks-immortal/

    Posted by Sunshine on February 1,2010 | 10:55 PM

    wow... what a life story for Hela and her family. Though I feel that her family should get what they deserve and live a more decent life, for the world truly owes big time from their mother.

    Posted by Mark Dennis Alcantara on February 1,2010 | 10:55 PM

    scary yet interesting story!! i have watch a mini series drama like this here in the Phils. produce by ABS-CBN channel 2 titled "my last romance" cast by luis manzano and toni gonzaga.. so when i read the word immortal i cNT STOP TO REA THIS

    Posted by cheryl daphne on February 1,2010 | 10:55 PM

    This article let me thank God for Institutional Review Boards (IRB). It is appalling how people's rights were violated in the name of research. Race and poverty are certainly issues here, and I hope the family never rests until they are well compensated.
    I don't think there is anything cool about profiting from people's body parts without their knowledge. What happens to morals? The scientists could at least inform the familyof their intent, or of what they did.

    Posted by T. Blair on February 1,2010 | 10:55 PM

    Very informative - I'm going to introduce this into out Black History Bulletin Board at church. Thank you.

    Posted by Gladys on February 1,2010 | 10:55 PM

    What an amazing story!

    Posted by > Rob on February 1,2010 | 10:55 PM

    WONDERFUL find. A job well undertaken.

    Posted by ben on February 1,2010 | 10:55 PM

    wow, this is like totallty AMAZING!!!!!!!!! When does the book come out, i would like to buy 2 copies, or is it already out? i cant get enough of this story.

    Posted by Keisha Simmons on February 1,2010 | 10:56 PM

    I'm a white American, veteran also. How many people receive blood transfusions so they can live in war or after an accident or a major operation? Do you think that a white so ldier who needs blood cares if a black American gives it to him or vice versa? I doubt it, and if the truth be known we would find out in a hurry that some of us have received blood from someone black or white. Human bodies don't care what color the outer skin of the person is, all it cares about is getting what liquid or solid it needs to continue to operate and live.

    What Henrietta had done is now wonderful for us all, but she died so others could live but not of her own choice, researchers the decision to investigate and take a piece of her tumor which resulted in these discoverys, many corporations have made large sums of money because of the tissue removal, and her family should have been given compensation before the companies CEO's and Vice Presidents received bonuses as a result of the research paying off.

    Posted by Ken Hartley on February 1,2010 | 10:56 PM

    Very interesting article. I think the family is owed money and much more, like an explanation. I would buy the book. Where can we purchase it.

    Posted by Bobbi on February 1,2010 | 10:56 PM

    It's amazing the cover ups that go on because of racism and racial biases. I used to live next door to a man whose father was the creator of the vaccinations we all received as children. This guy had a job at Frito-Lay, but he also owned 2 cash paid Corvettes. He eventually married and began a family, sold his house in our middle class neighborhood and bought property (a small estate) for his family to grow into. Often in medical science it saddens me to hear and see the vulturism that goes on because of race. Why wasn't this (black) family able to benefit the way I saw my (white) neighbor benefit? He was able to live his life in peace and prosperity because of his father's contributions to medical science, so shouldn't it be the same for the Lacks'? Even the author of the article tries to imply the family became consumed with retribution. She's making money via this book and its sales, why shouldn't the children and husband be compensated for loss and the bravery it takes to overcome that loss while understanding what their mother's miracle will do for others? Why should race matter when the world is being saved?

    Posted by Nicole on February 1,2010 | 10:56 PM

    People can be so typical at times. Getting angry, wanting compensation and for what? For those who are concerned whether the family did in fact receive any financial restitution can buy the book, but before doing so make sure a percentage of the proceeds are going to the family. I feel the scientific community did this to gain knowledge not financial gain. This is the land of opportunity, not compensation!

    Posted by George on February 1,2010 | 10:56 PM

    very noble, but it seems to me that this family was and is being treated like miss henrietta lack was, a black guinea pig, with no name, no respect, no compensation. I am ashamed of the american mentality at work here, glossing over this families plight, and profitting from their misery(typical). These folk are owed big time. I won't ask how these people can sleep at night, it is in their upbringing and make up, no mystery there.

    Posted by carlos on February 1,2010 | 10:57 PM

    I would like to thank Ms. Skloot for her persistance in following this story and uncovering the truth. This story is another example of how Black America has been ripped-off all these years of their accomplishments. Granted, Mrs. Lack did nothing by died and gave the medical community a map to many medical discoveries. Shame on everyone that took part in this cover-up and not recognizing this Black Woman and depriving her family and the world of this knowledge. Again thanks, Ms Skloot and I will certainly purchase the book.

    Posted by William M. Harris on February 1,2010 | 10:57 PM

    The government should award the remaining relatives a grant, bc of this family for their contibution to modern medical science. Their genetics have saved countless lives and have made countless advances available

    Posted by jameelia on February 1,2010 | 10:58 PM

    I feel if she had agreed to donate the cells hoping science could learn from them, possibly even find a cure...many of us would look at this story differently. In this situation, her cells were taken without consent of any kind. I think it is important that we realize the difference between donated tissue/cells vs stolen tissue/cells.
    I plan on being an organ donor. This of course means donating my organs. If something from my body can help mankind, I think that would be great! I would not expect for my family to be compensated. I would feel differently about that, if my organs were taken without my consent of donating them!
    Since hers were taken without consent, I would like to see a Memorial Fund set up where a percentage of the proceeds from the story benefits her spouse and children...and possibly even a percentage going torwards a scholarship (named in her honor)for those who want to study to find a cure!

    Posted by Tammy Morris on February 1,2010 | 10:59 PM

    Great story! I personally know Henrietta Lack's grandson.

    Posted by LRB on February 1,2010 | 10:59 PM

    Great Story...

    Posted by Rose on February 1,2010 | 10:59 PM

    Science can be very intriguing at times. amazing...

    Posted by lose belly fat on February 1,2010 | 10:59 PM

    The Henrietta Lacks story and legacy has fascinated me for years. I've written about it too in a book of poetry that addresses the history of African-American medicine titled "Elegy for a Scarred Shoulder" (2008, Aquarius Press.) Bravo to the Smithsonian for publishing this article and to Rebecca Skloot for a project that is long overdue. Karen S. Williams, author of "Elegy for a Scarred Shoulder." www.kswpoetry.com

    Posted by Karen S. Williams on February 1,2010 | 11:00 PM

    Grea Article....... I love it!!!!! :D

    Posted by Bea_13 on February 1,2010 | 11:00 PM

    From what I've read the cells were not donated for scientific purposes, they were harvested by DOCTORS. If they were taken and used for any purpose other than trying to help the poor woman get better from her cancer it was wrong.

    To profit and then hide the fact that this woman's cells were used in such an unethical way highlights all that is wrong with the scientific and business community. The fact that they lied over and over again about who she really was indicates that they knew that their actions were wrong and possibly criminal.

    Posted by David on February 1,2010 | 11:00 PM

    Vampire cells

    Posted by Tristan on February 1,2010 | 11:00 PM

    This was a very good article. I currently work in the medical field and know the benefits of HeLa cells and the research that was done with them. I would like to say some of the terms in the article and comments bothered me. In the 1950's, scientists didn't steal tissue, it was very common practice to take pieces of tissue from anything unusual removed from patients as a way of learning from it. Has it not occurred to some of you that the cervical cancer she died from still exists and has no cure! Even today, most people are not compensated for giving to science. It doesn't matter what race we are and making this about race is really sad. This is about science and the need. We are much more careful now and laws are in place for this not to happen today, but no one was trying to "harm" this woman. Her cells along with many others have helped us more then most people can ever know.

    Posted by Kandy on February 1,2010 | 11:00 PM

    This story is super interesting and opens the door to many questions.I did make an observation though,not one single reference to god in this very extensive list of comments is it possible that most religious people are not interested in science and therefore are so blinded by faith they don't want to hear anything that might shed light on the many THINGS WE DO NOT KNOW??????????????

    Posted by dan on February 1,2010 | 11:00 PM

    We are wonderfully made! We cannot be created by man...our cells may be manipulated and studied by man....but not created! Wow what a story...!

    Posted by Alvin Freeman on February 1,2010 | 11:00 PM

    I first read about this story in Oprah's magazine. I was really quite fascinated with it. I, too, would like to know if the family was ever compensated. I do plan on purchasing the book. I hope her cells will become a viable part in the cure for cancer.

    Posted by Michele Whitted on February 1,2010 | 11:00 PM

    Will Henrietta's family ever be compensated? It would be the right thing to do.

    Posted by Angela Ohanian on February 1,2010 | 11:00 PM

    is this book already available in amazon or e bay???????

    sounds interesting.....

    Posted by ckrizhnielle on February 1,2010 | 11:01 PM

    Reading this article makes me want to read this book ASAp, when is the book coming out can't wait to buy, I sure the family got something out of it, or they probably still waiting.. Tis sounds like a supreme court hearing..

    Posted by lyris on February 1,2010 | 11:01 PM

    The family should get free medical care in perpetuity from John Hopkins. That is only fair.

    Posted by Prish on February 1,2010 | 11:01 PM

    wrong,technically they are "immortal". the reason being is that they are cancerous cells, and cancerous cells multiply rapidly uncontrollably which seem like they're immortal. right they can die eventually but there's just going to more replacing the ones that have died.

    Posted by wilster on February 1,2010 | 11:01 PM

    Wonderful story! But, by the way! I hope the family was compensated! Especially after the scientist have taken a tissue sample from her without her/and families consent! - That is so sad!!!

    Posted by Judy on February 1,2010 | 11:02 PM

    VOW IT IS A WONDERFULL EXPERIMENT AND AMAZING RESULT.

    Posted by Ouseph on February 1,2010 | 11:02 PM

    Let's not tarnish scientific advances by calling it a race issue.

    Posted by cara on February 1,2010 | 11:02 PM

    very good storie. it may help someone . im very much into true medical inforamation that can help people to prove there life. sicence has come along way

    Posted by leeann on February 1,2010 | 11:02 PM

    OMG!!!! this is amazing i need the book nd i need o know if the family got their deserved money! now i have to take a bio class & learn more!!!

    Posted by Jasmine Hill on February 1,2010 | 11:02 PM

    Thank you Rebecca for such an amazing book and the findings of a great woman that will forever change the world. You are an amazing women for writing and getting it publishe for the world to see and learn. The family must be in awe of you. The family is sooo deserving of an outpouring in generosity wether it be gifts of love, concerns or moneys that is definetely deserving to them

    Posted by Angela Fisher on February 1,2010 | 11:03 PM

    this is so sad that this lady died but we love her in are heart she will be there for are life i love that how did she die but i did not enough of the story

    Posted by danei smith on February 1,2010 | 11:03 PM

    wow very nice and interesting story, hope after all it can really be a source of cure and help to a lot of diseases now a days...we should honor Mrs, Lacks the source of amazing Hela cells,and i think it is just right to give something to the family in honor of Mrs. Lacks i think she would be happy in heaven if her family is ok as well as those who have benefited her amazing Hela cells or Heal cells...

    Posted by Liv on February 1,2010 | 11:03 PM

    Inform consent procedure should have followed. However, it was good insight on science part. The article is well written. The is a nice way to start black history month. The book will be a must read for me. Hopefully, Henrietta's family got compensated.

    Posted by Sharon Sharon on February 1,2010 | 11:03 PM

    Well hello everyone and im going to be on this site only to post comments and answer's.Ok first off her cells are unique and interesting but theres always curious nature in interest so any questions get to me on dr.drew_help1@yahoo.com

    ...Thank you and Goodbye.

    Posted by dr.drew on February 1,2010 | 11:04 PM

    wow! very interesting and lots of good info. A real eye opener for people too. This would be great for a based on a true story movie. The family would be able to benefit from it.
    Thanks for this interesting story.

    Posted by anna r on February 1,2010 | 11:04 PM

    an absolutely unbelievable story! wow, her cells never died. makes me wanna buy d' book!!!! whoa...

    Posted by Karyl Encarnacion on February 1,2010 | 11:04 PM

    Very interesting and commended for reading for such a person contributes to our scientific research and commendable to everyone's knowledge and capabity.

    Posted by isabelo v.domingo,jr. on February 1,2010 | 11:04 PM

    Would make a great lifetime movie.

    Posted by eileen k on February 1,2010 | 11:04 PM

    My aunt is a teacher and she's read the book,the Lack's family is not entitled to anything,because Henreitta was compensated for her time,she just wasn't told about what was being done with her cells. Besides she didn't even know what a cell was, she was a poor black woman living on a tobacco farm. Should the companies(most of which didn't exist yet in 1951) that benefit from doing research on her cells have to compensate her children and grandchildren after she's been dead for 50+ years? Of course not. Besides the law(s) are in their favor regarding this issue anyway.

    Posted by Seantoe on February 1,2010 | 11:04 PM

    SIMPLY ANOTHER EXAMPLE OF HOW AFRICAN AMERICANS, BEFORE THE CIVIL RIGHTS MOVEMENT, WERE MANIPULATED & TAKEN ADVANTAGE OF BECAUSE OF THEIR LACK OF PROPER EDUCATION & ACCESS INFORMATION.. SMH, WHITE PPL!! --THANK YOU MRS. HENRIETTA LACKS--

    Posted by Faith G. Fletcher on February 1,2010 | 11:04 PM

    I just read most of the comments posted so far. What a diverse colection of facts opinions and rebuttal.Please stop to think where we would be if the cells were not used... and this type of cell went undiscovered. I venture to say life as we know would be very diffrent for all of us.This transends race, gender and every other hurdle mankind faces and has faced. Have you ever seen or known a person thats contracted polio? or a host of other diseases including cancer research just in itsself... can you really comprehend the ramifacations of what this has brought to the table for ALL of us? giving back knowing or unknowing is human nature in its purest form. Has anyone ever reached out to help , honestly help some one even if they appeared to not need it. and ask for somthing in return??... this lady died from the same culture that was taken from her iand it gave life to millions i doubt she would have asked for money or even excepted any if she was told what would be possible to accomplish with the sample .please think about it it didnt matter what color she was that never was and issue till now in the perverted minds of people that want all they can get with no cost to themselves.

    Posted by hereintexas on February 1,2010 | 11:05 PM

    Oh My God! (OMG)this is amazing! incredible! how could it be that a cancer patient cells had lived for so long...imagine 25 years!!! the people behind this research should give some monetary compensation to the family of the late Henrietta Lacks (peace be with her)...this story must get a prize from the publisher...long live!

    Posted by Rojaida M. Maliga on February 1,2010 | 11:05 PM

    I glance at the picture and kept going to facebook but something about it had me going back to the story and wow what a story! I am looking for the book soon as i get off here.The things that some people do to keep things under wraps.I hope the family fights and get every penny they deserve.the man buried his wife once now he and the family have to deal with this.Some people just dont have a heart that they was born with to do this.

    Posted by laura on February 1,2010 | 11:05 PM

    It's awful that Mrs. Lacks had no knowledge of this act and now her cells are being sold. Her family should never give up the fight for 1/2 of the money earned in the sale of Mrs. Lacks cells. They are entitled to 1/2 and pain and suffering since her children didn't have the opportunity to know her. If complete strangers to the family can earn money off of her cells and their invaluable research they have provided for the human race, then they should be able to collect. Go Lack Family and NEVER give up!!!!

    Posted by Debbie Berk on February 1,2010 | 11:05 PM

    that is freeky but amazing

    Posted by manuela on February 1,2010 | 11:05 PM

    another reason why african american are skeptics of medical research.

    Posted by ACDEXTER on February 1,2010 | 11:05 PM

    This is a very interesting article. Now I want to read the book!!

    Posted by on February 1,2010 | 11:05 PM

    Wow, it is a one of a kind story, amazing, hope to get that book. It sounds scary though,It reminds me of movies like resident evil, dawn of the dead, were cells leave though the body is dead. So, scary.

    Posted by lloyd on February 1,2010 | 11:05 PM

    Sarah, Wow that was a great article. Thank you so much for caring about and researcing history. The family should be honored her cells were of beneficial value to those in need. Janet

    Posted by Janet on February 1,2010 | 11:05 PM

    They are immortal cells because they are cancer cells. Cancer cells have lost the gene that programs them to stop dividing. Hela cells like all cancer cells will always divide that is why they are immortal.

    Posted by monique on February 1,2010 | 11:06 PM

    22o b to? or jst part of the book?

    Posted by Chakie on February 1,2010 | 11:06 PM

    Pretty lady, handsome husband, beautiful contribution to science, tenacious researcher, great comments. Praise be to GOD the creator!

    Posted by E. moma on February 1,2010 | 11:06 PM

    This is such a great story. I'm very amazed on cells works now. I love this story and I hope that you find more stories like this. Thank you for sharing this story.

    Posted by Roxy =] on February 1,2010 | 11:06 PM

    YES Confirmation i heard that after extensive studies that humans have nothing in our DNA that tells us to age. grow and mature yes but not age so i figured the only reason we age is because we believe it and therefore of course the cells can be immortal for there is no brain to tell them to age and die.

    Posted by Magenta on February 1,2010 | 11:07 PM

    Wow, nearly everyone who commented here (including her some members of her family, according to the article) sees dollar signs! As if something like this can be equated to dollars and cents. Not everything in this world carries a dollar sign! The doctors took tumor tissue. It wasn't like they took a piece of her healthy brain or her healthy bone tissue and sold it. It was diseased tissue, and doctors remove this kind of tissue all the time from patients...and don't pay them! If anything, I hope that the author of this book gives the ones in the family who were willing to work with her some compensation for sharing their story. It is a fascinating story, and I look forward to reading the book when it comes out!

    Posted by Jella Ambroglio on February 1,2010 | 11:07 PM

    This family should be paid for their mothers cells. What the researchers did was stealing.Someone should go to jail for this act.This is about more than research.!!!! I am mad as hell about this!!!!!!

    Posted by tony on February 1,2010 | 11:07 PM

    I guess the first thing I want to say is, Thank you Henrietta! God Bless you! I'm sure you are watching from above.
    What a difference she has made to us all. Great story. I feel it only right the family should be compensated. People can buy the rights to songs others have done and receive royalties. Writers can get compensation for plagiarized works. How can anyone argue her family is not entitled to a percentage of all these transactions? It was done without consent. Henrietta never signed over anything.
    I will definitely read the book! Wishing the best to all her family!

    Posted by Robert on February 1,2010 | 11:07 PM

    I have always worried that someday I would have to pay for my excellent health. I never had any of my childhood dieases and didn't avoid my children when they had them. I never missed a day of school in 12years due to sickness. I worked for the same company for 36years and never missed a day to sickness.I am 71years 0ld and just got the results of my physical-eccellent.My doctor says I must have some good genes. My question is,would they be interested in studing my cells? I think it would be a honor to do something like that for humanity before I die.why wouldn't we want to save lives?

    Posted by harvey d neill on February 1,2010 | 11:07 PM

    Too bad!taking even a little piece of a womans body without asking permission to the concern is unhuman. even the cells is very useful but the fact that the scientist is not asking permission is not good example.then other people makes a lot of money from it and the family is still suffering from poverty. To the family of Herietta Lacks, fight for it you have all the rights!

    Posted by JOY on February 1,2010 | 11:08 PM

    Great piece. And yes, the family deserves to be compensated. Largely compensated. There's nothing wrong with this, as it happens all the time with medical malpractice, which is exactly what this case is. We're not usually made aware of them. Mrs. Lacks was disrespected, while dying from cancer, because of racial (and gender) politics of the 1950s. When we still had colored water fountains. Those existed in the 1950s too, but at least now most people would think those were wrong. So are the actions of the doctors directly involved, the hospital administration, and all the companies that bought the cells and applied a code of silence on both the purchase and use of the cells to Mrs. Lacks' family for decades. This is not a case of a black person getting money for nothing, or a tragic yet inspiring story that needs to invoke affirmative action anger. Redress the wrong done to Mrs. Lacks in the 1950s by making her story more than well known, and compensate the family for this egregious case of malpractice. In the meanwhile, let's celebrate this woman, who, while not being able to choose to be a great part of history and saving millions of lives, nevertheless has been and should be respected in a way denied her sixty years ago.

    Posted by N. Orton on February 1,2010 | 11:08 PM

    what a story! Amazing!

    Posted by shekhar on February 1,2010 | 11:09 PM

    This was an interesting article. It clearly points out to important details to me. One thing is that some people comment about it being about money and that is all the family care about. Honestly the scienctist were dishonest, by stealing a tissue sample, one because they looked at her as just a poor uneducated black woman, who wouldnt know what was going on. Which was wrong. The sample helped create a vaccine and so on, but these men knew it would generate millions of dollars, and they were greedy making these discoveries and not being thankful to this family and compensating them, considering that they new times were hard for the family, and there loss of a wife and mother. i do not blame the family for being upset. In the same aspect im sure the family is thankful what there mom contributed to many and millions of people. The writer states its not about racism, but i ask the writer how could this not be about racism and greed? My blessing and prayers go out to her family and hope that they are acknowledge and thanked they way they should of been in the first place.

    Posted by christy on February 1,2010 | 11:09 PM

    Today I thought I'd learn something about Black History. Didn't know what or when but I am glad it was this along with the celebration of the F.W. Woolworth ceremony. Thank you!!!

    Posted by Vincent on February 1,2010 | 11:09 PM

    wow!..this is a breath-taking story i ever read in a lifetime..knowing that many lives being saved by this "hela cells" which came from human cells is a great story..thank you for the wonderful story ms. rebecca skloot for being a good researcher and a writer..i must say thank you also to ms, henrietta lacks for saving lots of lives..mabuhay!..on behalf of the filipino people, i must say "THANK YOU HENRIETTA"

    Posted by Lucia Aguelo Sedon on February 1,2010 | 11:09 PM

    Please don't publish my full name. You can use Carl or C. Purv, or some short version like that.

    This is really an interesting story and particularly to me, since I'm 77 and my body will be donated for study to the local med school. I wanted to be an organ donor, but now understand that donor organs are not accepted from donors my age. That's O.K., too, but now I'm more iterested in the benefits my cells, tissues, etc. may offer to make life easier for someone in the future and possibly aid in developing new medicines or treatments that can help others. Thank God for what has been learned from Henrietta.

    Posted by Carlton Purvis on February 1,2010 | 11:10 PM

    great story,unforgetable

    Posted by leorama on February 1,2010 | 11:10 PM

    very interesting

    Posted by Xavier Rainwater on February 1,2010 | 11:11 PM

    While I am thankful that Henrietta cells were available towards new discoveries, I am sadden and dissapointed of the way it was made available. Because of this, I believe that the family should be compensated greatly! Interesting article, but even the writer of this book is making money off of Henrietta story and not the family, again.

    Posted by Sabrina on February 1,2010 | 11:11 PM

    I've been working on HeLa cells for over two year now and those are a HECK of a culture!

    Posted by Jargin on February 1,2010 | 11:11 PM

    I'm taking Microbiology, Genetics, and biotech class. I was just reading about this in the book. When I went to Yahoo, a link to this article was part of the headline. I click on and just decided to email this link so I can print it out to show to my professor tomorrow. This article looks so freakin cool.

    Posted by Michael on February 1,2010 | 11:12 PM

    I love the story. I think that scientists still have a lot to find out about the existence of human being. This may be a great way to start.

    Posted by Vani Bogin on February 1,2010 | 11:12 PM

    As much as we all thrive on scientific research done everyday in laboratories to help human race survive, it is sad how ignorance can lead to greater difficulties for families involved in such research.

    Posted by kc on February 1,2010 | 11:12 PM

    Incredible story ! Life - cells.

    I think it is Terrible thou that her family did not Know, scientist were experimenting with her mother cells,after all these years.
    And made $$$$ off Henrietta Lacks Body.

    Posted by Teri on February 1,2010 | 11:12 PM

    excellent just excellent, i want the book asap. i hope the family got something from this

    Posted by jeff ayema on February 1,2010 | 11:12 PM

    PAY THE FAMILY! PERIOD!

    Posted by Abel Rodriguez on February 1,2010 | 11:13 PM

    Nice. Somebody needs to pay the family.

    Posted by Southern girl on February 1,2010 | 11:13 PM

    awesome story...

    Posted by khaulah on February 1,2010 | 11:13 PM

    I have recently wondered if cancer might be spread through the air. I know a pulmonologist who died from Lung Cancer and never smoked. Another pumonologist died from Stomach Cancer. I wonder if during their surgeries, cancer cells were inhaled and maybe that's how they acquired cancer. Now, I am even more curious since Henrietta's cells were found in dust particles! At any rate, I am an African American woman and I am very proud that Henrietta contributed to science in this way. My only hope is that the family will be compensated and that now it is mandatory that patients give consent prior to be enrolled in a scientific test!

    Posted by Kim Poellnitz on February 1,2010 | 11:13 PM

    nice story, but nobody owes the mother or descendants any money. you dont have a property interest in "cells" collected like a cancer tumor. Once you willingly "give up" excised tissue, you no longer have ANY property rights to the tissure.
    google search greenberg vs miami childrens hospital.
    also look at moore vs regents of university of california.
    these are landmark cases that pretty much decided these issues.

    its a nice story, because a black person is involved, and people always like to say the white man put down the black man...but it isnt the case.

    its can get more complicated when the tissue is from two people (an embrio), but for the case at stake...they are not owed any money.

    Posted by mike on February 1,2010 | 11:13 PM

    WOW!!!! I LEARNED SOMETHING NEW TODAY. VERY INTERESTING...I NEVER EVEN HEARD OF HER. BUT I'M GLAD HER CELLS ARE AROUND TO HELP US TODAY, AS WELL AS IN THE FUTURE. :)

    Posted by MRS. JONES on February 1,2010 | 11:13 PM

    Great story! But how about the fact that the cells were taken without permission and used successfully in scientific research? Shouldn't they compensate the family? I shudder to think that this may just have been one of those conspiracy things that America is fostering on its own people to rob them of their rights. And those attempts at bullying third world countries to give up their intellectual property rights in the name of scientific research? If you take something, you give something back. I hope the family has been rightly compensated and formally acknowledged to have helped the scientific community and the world.

    Posted by Pablo Mercado on February 1,2010 | 11:13 PM

    Yes,

    This story is just another example of using people of color as uncompensated and unethical guinea pigs. If all the secrets of medical research were exposed it would cause a catastrophe. Those doctors, as well as the author is completely soul-less. End of story.

    Posted by Marcia Bell on February 1,2010 | 11:14 PM

    what an amazing story...
    I just hope that Henrietta Lacks' family would get something... for them to live comfortably...

    Posted by k12b26 on February 1,2010 | 11:14 PM

    This is such an incredible story. Immortal cells! Who knew?! Its so sad that her family couldn't understand the importance of their Mom's contribution. The actions of the scientists toward the family disturbs me.

    Posted by C. Rob on February 1,2010 | 11:14 PM

    I enjoyed this article a great deal. I believe the author did a great job, thank you. Likewise, as I am sure you know, Ms. Henrietta Lacks like so many other Afro & white-American people of the day were subjected to horrible medical experiments. Please note, medical experiments in Mississippi, Alabama, University of Rochester (Rochester, NY)....

    Posted by Cletus Whirl on February 1,2010 | 11:14 PM

    To all of those people wondering if the family is entitled to anything such as restitution or a frivolous lawsuit - I only have this to say: You are probably alive today thanks to what that scientist did. And that should be payment enough. Give them a plaque and maybe a dinner and call it a day. Give me a break. What kind of society would we be if the only reason anybody did anything was to garner profit??? Shame shame shame... think before you speak.

    Posted by Jennifer Mavens on February 1,2010 | 11:15 PM

    Sure...it definetly makes me interested in the book...but it more makes me want to quite going to the doctor!!

    Posted by Kim on February 1,2010 | 11:15 PM

    what a gift this woman has given to mankind! thank you henrietta! you would think that some compensation, a royalty for use, could be given to her family. any compensation for colaborating on the book?

    Posted by deb on February 1,2010 | 11:15 PM

    i have never an article in full on yahoo or anywhere else online, but once i started this i just couldn't stop... Bravo Sarah... I f you were a writer i will not stop reading your books, this piece is very interesting... btw, i have never ever left comments either on any article online. Good job!

    Posted by DADA on February 1,2010 | 11:15 PM

    WOW!!! What a GREAT article-just in time for Black History Month!!! I agree that this article/also the book should be required reading for students,regardless of their ethnic background-to prove to the "non-believers" that the Black Race has contributed in many ways to the makings of mankind world-wide,some without recognition!!! I plan to buy this book,and as someone previously mentioned"perhaps Oprah will give it HONORABLE MENTION on her TV Show" Also,I pray the family of Henrietta hasbeen/is being compensated financially for their mother's great contribution to our world. I and ALL of my family salute you Henrietta even though your idenity about your cells, because you were a Black Woman,were hidden from the world-UNTIL NOW!!! BRAVO!!!

    Posted by Ellen Burks on February 1,2010 | 11:15 PM

    CONDUCTED RESEARCH CALLED [ TOXICITY STUDIES OF EPOXY RESINS ], I USED HE LA CELLS, WAS TOLD THEY CAME FROM A PATIENT WHO DIED OF CANCER. WHAT A STORY, BRINGS BACK MEMORIES OF THIS STUDY.

    Posted by Dr, PETER KAPSIMALIS on February 1,2010 | 11:15 PM

    I am a cancer doctor and researcher. I was blessed to work with HeLa cells in the lab in undergraduate and graduate school. This woman contributed so much to the understanding of science with a few of her cells.

    Posted by Kathy on February 1,2010 | 11:15 PM

    Well...I believe back in the days there was not a big issue taking a sample of her tissue without her peermission. She had cervial cancer and she would die anyways. Comon guys, if you have cancer in the 50's, you would most likely die.
    I agree that she made an invaluable contribution to the science, but her family making law suit and claiming $$$ is ridiculous.The 50's, 60's, 90's and so on are very different period...so get over it!!!!!

    Posted by James on February 1,2010 | 11:16 PM

    this is a well written book,when is it coming out and what is the title.its a book worth reading.and behold science is beautiful and GOD is awesome.

    Posted by sholakunmi on February 1,2010 | 11:16 PM

    The number of people asking about compensation to the family is dismaying. With all due respect, why should the family receive money for something they had nothing to do with? Whether the doctor should have received Ms. Lacks' or the family's permission to take a tissue sample has to do with laws AT THAt TIME and nothing to do with paying money to family members NOW. While I don't understand many readers' entitlement attidue, I found the article very interesting! Thank you.

    Posted by Rebecca on February 1,2010 | 11:16 PM

    First of all I want to thank Henrietta and God Bless the family. I found this to be a very interesting article. I don't think that race played a factor in this. I think there are alot of similar situations involving white people. We just don't know if any of the cells taken contributed as widely as the HeLa cells. For instance I am white and I had a brother born stillborn in the late 50s and when my mom wanted to see him they wouldnt let her. They told her that he was dead and they needed his body for science. They told her she didnt have a choice and that all stillborns were to be kept by the hospital. They took advantage of a young mother and bullied her into leaving him with them. They only let her see him for a few seconds. She was very young and she herself only had a 6th grade education. Now my family grew up poor and we had to make our own way just like any other honest person. It was an unthinkable situation just like Henriettas.

    Henrietta earned her recognition there is no doubt but I dont feel like the family should have free health insurance no more than the rest of us poor folk.
    You have to work for what you get and you get what you work for. You take any hardworking woman or man from the 50s (black or white) and they were proud and would not accept handouts for something they didnt earn.
    If a doctor takes cancer cells out of me I definately dont want them back.....

    Posted by Arial on February 1,2010 | 11:16 PM

    i don't read much but this story caught my eye so i began to read.this story truly is remarkable i can say looking forward to the book

    Posted by henry on February 1,2010 | 11:17 PM

    Compensate the famiy. It is the right thing to do. They should not be made to unwittingly pay a cost (not just once but twice) with no renumeration. It is beautiful though what has been accomplished due to Henrietta Lacks' contribution.

    Posted by Lone Wolf on February 1,2010 | 11:17 PM

    Amazing story... it's too bad that some people can not see the big picture but only dollar signs and playing the race card.

    Posted by ZeeBop on February 1,2010 | 11:17 PM

    Im not sure if my post posted soooo......

    Hela cells are "immortal" because they are cancer cells. All cancer cells have lost the gene that tells them to stop dividing so they will continue to divide forever if the condition is right. That is why cancer cells create tumors because they continuously divide.

    Posted by Monique S on February 1,2010 | 11:17 PM

    Amazing story. Her family should be proud. Can't wait to read the book. Where can I find it? I hope her family received some monetary compensation.

    Posted by Patsy Y. Sawyer on February 1,2010 | 11:18 PM

    i actually read about this 20 or 25 years ago in an article in Reader's Digest while waiting in a dentist's office. i remember feeling a sense of outrage that the family never received any compensation for the use of the HeLa strain cells. if it truly benfited society to the extent the author implies, they are certainly the LAST family in america that should be living in poverty.

    i won't call this a race issue, it's a class issue. property rights are supposed to be so highly regarded in this country, but this case proves that only corporations have those rights assured to them under the rule of law. effectively, in the eyes of the government, individual citizens are not even granted the right of ownership of their own bodies.

    this is a miscarriage of justice that must be redressed.

    Posted by Erik Leifsen on February 1,2010 | 11:18 PM

    Not to offend anyone, but I don't see that Henrietta Lack did very much here. I mean, if we're looking for heroes, let's look for people who actively did something, knowingly, consciously. Yes there's obviously some power and race dynamics at play here. No doubt about that. But until the samples were "taken" and tested, there was essentially NO value to them. I don't know enough about HeLa cells to know if they were absolutely unique (in which case many different cell lines must have been tested and rejectecd, and in a way ALL those other lines should ALSO be "compensated," as being part of the overall scientific endeavor) or if they just happened to be in the right place at the right time. It seems to me that the ones who did the real work and who should be celebrated are those evil "white scientists" who while ONLY interested in reaping huge profits somehow managed to stumble on some actual cures for some actual diseases.

    From what I've read here it doesn't seem like there should be any compensation. It's sadly ironic that some of Lack's heirs are living without health coverage, when her cell lines have done so much to advance modern medicine. But I think it's sad that MANY of us are living without health coverage. The answer to the perhaps unethical "taking" of Henrietta's cells should not be to shower riches on ONE family (when their role in the whole affair was essentially accidental). A better legacy would be to see that we are all connected and that we ALL deserve health coverage as a basic human right, not just this single family.

    Finally, the idea that the author of this book owes a penny in "royalties" to anybody is LOOPY. Nobody had to talk to her if they didn't want to. Reporters have the right to research a story and publish their findings. Those who so blithely opine that the author should compensate Lack's heirs should really consider the chilling effect such a policy would have on the practice of journalism.

    Posted by Garret on February 1,2010 | 11:18 PM

    With regard to the family sharing in the millions made with research, remember it was not the cells themselves that made so much money, but the research and experiments, including cloning, which also has a very high investment cost. My daughter has a very rare syndrome and has several times freely signed consent forms for research to be done with her tissues with no compensation attached. Because Mrs. Lacks' story is so interesting i would think proceeds from the sale of her story would be the place to start for compensating her husband, if still alive, or if not, then the children, provided they contributed to the telling and research for the story.
    I appreciate the author's desire to not villianize scientific research.

    Posted by Gay Hayes on February 1,2010 | 11:18 PM

    this is a good scientific adventure,but taking some thing from someone without permission is a criminal act,secondly,i know someone somewhere is making billion of dollar from that black woman cell whose family members are suffering without saying thank you or even compensation package to the family.

    Posted by cy on February 1,2010 | 11:18 PM

    I remember writing about Mrs. Lacks back in the early 1990s, when I was working for _Destiny_ magazine. I recognized her picture -- it's the same one we used.

    Funny how it takes people so long to catch up!

    Posted by BVL on February 1,2010 | 11:18 PM

    wow i'm 13 an i found that interesting. i have got to tell my science teacher.on the other hand that is toooo freakish. that is totally a book i would want to read i've got to find that book right now.TELL ME WHERE IT IS...TELL ME TELL ME TELL ME!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!

    Posted by requsha dailey on February 1,2010 | 11:18 PM

    Why are her cells immortal? I don't see this in a financial way. I think the family is (should be) more interested in the why's and how's. Personally, I would feel a great sense of pride.

    Posted by Stephanie Casey on February 1,2010 | 11:18 PM

    I think it is amazing to see the Henrietta is a black woman. I know in my Biology class there is no mention of her being a black lady in the book. She even looks like she could possibly be white in the book. I would love to buy this book. Can someone tell me where to buy it? For the two comments stated that Ms. Lack is a "vampire," I think you should keep your comments to yourself. The comments are not funny and no one is laughing with you (just your stupidity). I hope the family were compensated.

    Posted by ROSE on February 1,2010 | 11:19 PM

    Henrietta Lacks spirit might be wearing that GREAT smiles now...

    Anyway, the family must be proud of her...and definitely, they are entitled for a monetary compensation for this...or whatever help they may require...

    I can't wait to buy this book...hope it will be available all over the world...

    Posted by gay marie jumuad on February 1,2010 | 11:19 PM

    great work!

    Posted by megs on February 1,2010 | 11:19 PM

    I appolagize, but this may sound a little morbid...but the first thing that crossed my mind as i read this story was what shape would her body be in if it were exumed. The fact that the "few" cells they kept NEVER died, leads me to believe that the other cells in her body would possibly be the same....is she eternally perfectly preserved? Like everyone else posting comments here, i believe that her family is entitled to benefit from any money made from thier mothers "contribution" to all man kind, and not to be left out in the cold by the medical conglomerants benefiting financially from the discoveries made from "her" cells!!!!

    Posted by Lisa on February 1,2010 | 11:19 PM

    i really liked this article, it was interesting but it really made me mad when reading some of the comments doing the whole "if she was white they would have said something sooner" or something in that nature. Its sad some people cant find something out even through science that help people and turn it into something racist, thats why this world is the way it is today.

    Posted by amber frye on February 1,2010 | 11:20 PM

    Some people must ALWAYS find some racial undertone to everything. This is a fascinating story, why ruin it with race baiting?

    Posted by Frank Carter on February 1,2010 | 11:20 PM

    i actually used hela cells today.

    Posted by zach on February 1,2010 | 11:20 PM

    This is a valuable article historically, especially given that most people do know the origin of the HeLa cells. In a sense these cells have an almost mythical status in biology.

    However the author and the writer should have done a better job of doing their legal and medical research.

    HeLa cells are "immortal" because they are cancer cells. Cancer cells do not undergo apoptosis, "programmed cell death," and will continuously divide on and on if given the right environment. Most normal cells eventually destroy themselves if they are too old or damaged. But in cancer cells this continuous division leads to a large number of complications which kills the individual.

    The sad fact is that back in the day most people died of ovarian cancer, as there was generally no effective treatment for it.

    Additionally, although it is sad that this woman was not told that cells were going to be taken from her and used in research, is it an unfortunate fact that this was an extremely common practice back in the day. Up until the 1990s, doctors and scientists regularly took tissue samples from patients without their knowledge. In fact, this was the issue of a lawsuit in the groundbreaking case of Moore v. Regents of California. In that case the courts ruled that a patient has NO PROPERTY RIGHTS over a cell line that was derived from their discarded tissue. Moore had sought treatment for his leukemia, and without his knowledge his discarded cancerous cells were used to create a cell line, which was commercialized and created millions of dollars worth of projects and products.

    Whatever you think of the decision in Moore v. Regents of California, what happened to Henrietta Lack also happened to many, many people.

    Posted by NathanB on February 1,2010 | 11:21 PM

    Wow! this article was amazing, it makes you want to buy the book! Its cool to know where everything began.

    Posted by Lissette on February 1,2010 | 11:21 PM

    WOW.... This was Very INTERESTING..... What is the name of the book? And where can I get a COPY.

    Posted by Erica on February 1,2010 | 11:22 PM

    As many before me have stated , fascinating, do hope the family get compensated to a degree, got to get the book.

    Posted by ArtLabo on February 1,2010 | 11:23 PM

    Great Article! This is really a very interesting story. I would love to know more & buy this book.I agree that the family deserves to get a share of amount.

    Posted by Joneth on February 1,2010 | 11:23 PM

    This story is so amazing to me. Did the family ever get any compensation? Are they still using the cells today? How do we know that the doctors didnt kill their mother just to get these cells? I would love to read the book.

    Posted by Janice Erby on February 1,2010 | 11:23 PM

    Wow, that article is very interesting. But i also wonder did the fam recive compensation? I mean somebody in that fam might also have immortal cells and that would be kool.

    Posted by rose on February 1,2010 | 11:23 PM

    A tumor was taken out of a women who died, and was used for science when this was an early area of medical work, and somehow she is more special than the rest of the people who the same thing has happened to?

    Her color doesn't matter (to those who you who feel compelled to bring it up), the level of ignorance of her family has nothing to do with it either. This story brings tears to the eyes of readers who live in a fish bowl. The rest of the world sees events in a larger context, simply as one of millions of events with science.

    Posted by Samuel on February 1,2010 | 11:23 PM

    This is a book I would really enjoy reading. I am going to try and find it.It's an amazing story.

    Posted by Linda S on February 1,2010 | 11:24 PM

    I don't know what the fuss is regarding compensation. I mean we are all just animals that are the product of evolution right? It's no different than working with cells from a lab rat is it? Neat story

    Posted by Heaterman on February 1,2010 | 11:24 PM

    Its seems like the family would have be compensated for the sale and passing around her cells, after all her husband offspring were still alive with these findings. But with this culture has historically treated people- they'll probably never see a penny. Interesting though.

    Posted by frit on February 1,2010 | 11:24 PM

    it is very interesthing story ...this story is good for the movie, many people can learn about this ..not only educated people also to the people that no read no right...also if this family of henrietta will be agree that hier mother story can be out as movie ..then they can have money for this so thier mother can help them even her mother is already deid...it is big help specially to henrietta family and also to the native people..you know what you can help alot of people if you going out this and make this as movie...you can get money for henrietta family as help for them ,not only money also knowledge..not only for educated people also to the small people...

    thats only my suggestion...but this story is really amazing...

    Posted by Baby Rose T. Allison on February 1,2010 | 11:25 PM

    OK, the study involving human cells is good for the humanity in the future. But, a lot of people (scientests) made a lot of money on the sale of HeLa cells. Why not compensate the children of Henrieta? They have lived in a poverty for so long. Make sure that the children gets some money, is human enough.

    Posted by Rafael Temana on February 1,2010 | 11:25 PM

    nice :)

    Posted by Ivee on February 1,2010 | 11:25 PM

    I love this story! I can wait to buy the book, I must send a copy to my doughter. WOW AMAZING !!!!!

    Posted by Fortino Gutierrez on February 1,2010 | 11:27 PM

    I, too, will purchase the book. As was and still is, people of color-particularly black people are being exploited in the name of and most science related studies without their knowledge. The sad thing is, it is government sponsored. Granted, we need research science to find cures, but don't come as a thief in the night and then try and dismiss what you were really after. There will never be full equality in our society, so, stop picking on the un-educated or the under-educated. That fosters distrust amoung that population.

    Posted by Emma on February 1,2010 | 11:27 PM

    This is an intriguing article, although I would believe that if we took the cells we would find that they arent truly immortal but just able to live longer, like a bacteria can out live a human and move on except these are cells. This is a very fascinating article/

    Posted by kelvin on February 1,2010 | 11:28 PM

    Very intersting story. Great the way one's human part can help solve mysteries in our medical world to help millions. Me think, it's a good thing. But the bad thing about this story is how Henrieta's living family was not interested about human genes until the money factor came to focus.LOL..Ahhh humans. Always thinking for themselfs and not others.

    Posted by Larry on February 1,2010 | 11:28 PM

    The book, The Immortal Life of Henrietta Lacks by Rebecca Skloot, is available on Amazon for $14.04. It also can be bought at Barnes & Noble.

    Posted by Will on February 1,2010 | 11:28 PM

    How is this information substantiated? In the book, are there pictures or images of original documents?

    Posted by Pat on February 1,2010 | 11:28 PM

    Her story should be tought in every school...

    Posted by Hakim on February 1,2010 | 11:28 PM

    Awesome story, but in answer to some comments, cells and race doesn't matter when it comes to science. When you have cancer in modern day they ask you if they can sample it for science and no you don't get paid you do it for posterity in hopes it will help someone in the future (at least that is what I hope for my cancer cells). God bless her children growing up without a mother and poor.

    Posted by sheila68 on February 1,2010 | 11:28 PM

    I am so excited to learn more about this biologically! Thanks!

    Posted by Makeda Young on February 1,2010 | 11:28 PM

    Hello!!!!!!!!!!!!!!!!!!!!!!!!!!!!

    How many more were there like H.L. Only GOD knows and we should know also. I will Get The Book!!! WE all should.

    GOD BLESS HER AND HER FAMILY....

    Posted by Terry White, Palmdale, California on February 1,2010 | 11:29 PM

    To the author: I really think this article is great. Thank you for actually taking the time and persisting to this extent. This is definetly another part of our Black History. I have to admit that the more I learn of our Black history and the way we were taken advantage of, it makes me proud of our accomplishments today "(OBAMA)" but it also makes me sad, mad and amazed on much is hidden in our past. I cant wait to read the book. The entire family should be compensated, its the least they can do.....

    Posted by Keila on February 1,2010 | 11:29 PM

    Hmmm okay so like is it just a myth for a human to be immortal or can scientist actually figure out a way using Henriettas cells?????

    Posted by Michael on February 1,2010 | 11:29 PM

    Ughh What happened? This is such a clincher!! I have to get it from the library (sorry poor grad student)to find out what happened. It is surely a great journalism piece. Along the way the Smithsonian just got a new subscriber :)

    TG
    Bronx, NY

    Posted by TG on February 1,2010 | 11:30 PM

    This article definately makes me want to buy the book. I have MS and firmly believe that the cure for any one of the catastrophic diseases (cancer, MS, lukemia, HIV, etc) will have a domino effect...find a cure for one, the cure for the others will fall into place.

    What a wonderful legacy for Henretta Lack! But I agree with the majority of responders and believe her offspring should have been and should be receiving compensation for her unauthorized donation to science. "HeLa cells were the first human biological materials ever bought and sold, which help launch a multi-billion-dollar industry."

    She paid with her life and her heirs should be allowed to live in some sort of comfort .... what would, say, even 1 or 2% of a multi billion dollar industry mean to her family's quality of life? What has her donation made to the quality of your life or someone you love or know? Smithsonian...are you doing anything to help this family?????

    Posted by Santina Ryan on February 1,2010 | 11:30 PM

    this sounds interesting i wounder who else is like that i think it would be kewl

    Posted by dustin little on February 1,2010 | 11:30 PM

    Facinating!!

    Posted by Debbie Sullivan on February 1,2010 | 11:30 PM

    It's not everyday u get a story like this so i'm raelly fascinated by HeLa's story and even the writer who was that determined to reveal this very inportant story that has been kept quiet for so long. BigUps...

    Posted by Daniel Olise on February 1,2010 | 11:30 PM

    makes me want to cry!

    Posted by dave young on February 1,2010 | 11:30 PM

    a very interesting piece!....i want to read further story about this henrietta....

    Posted by analou dumanig on February 1,2010 | 11:32 PM

    ...After all the scientific breakthroughs her cells have brought to humankind I think it would be nice to offer a moment of silence for Mrs. Henrietta Lacks...

    Posted by Veronica on February 1,2010 | 11:32 PM

    This story is very educational. It touches on what can be done in terms of research and science. It also touches on the ethics of the medical field. I think the family is owed money. They werent given the chance to choose. It helped the technology of medical research. Yet there was no recognition to the source. I will read the book.

    Posted by kristy on February 1,2010 | 11:32 PM

    so amazing of the true storey of the immortal cells of Henrietta Lacks and how it has scientifical study help the whole world how ever takeing ms Henrietta Lacks cells with out permission1 and 2 with out notifying her family after & 3 the most outrage selling the cells of billions of money with compensation to the family is outrageous greed and selfish and wrong regardles how you sugarcoat the fact of the matter very disgrace. my heart goes out to the family.

    Posted by james on February 1,2010 | 11:32 PM

    excellent account of medical history. i worked on research projects using HeLa cells on three occasions, once to find a vaccine for influenza A2.
    at the time, removing a small sample of excised tissue was considered no more immoral than, say, saving fingernail clippings or a tress of hair.what is amazing is that undifferentiated tissue, which is what a cancer is, should live this long in the very same form, with the same qualities and stability. the expectation is that the tissue would just die, but it didn't and hasn't and evidently won't.

    some may now see it as immoral, unethical, racist, financially unjust. i cannot judge these things. i am just grateful to mrs. lacks for having lived, albeit far too briefly.

    Posted by carole jordan on February 1,2010 | 11:33 PM

    Wow, what a facinating story! I will definitely buy the book so that I can learn "the rest of the story." Thank you for having the insight and the tenacity to persue this story. And , a huge "thank you" to Henrietta for her valuable contribution to mankind.

    Posted by sunny m on February 1,2010 | 11:34 PM

    look for what reason is race even in this. does anyone know how many women were treated for this same thing in 1951. and whether they were black or white does that matter? or for that mater if sampels were taken from the other women ? and not told about it. did the doctor actually right down in a journel that she was not asked first is there proof,im saying that she did not give her permission? lets get over this whole race issue and celebrate a woman who possibly new they were going to take the sample and as an outcome saved many lives

    Posted by brad on February 1,2010 | 11:34 PM

    Why should Henrietta's family be compensated? They did nothing to earn the money. Nor were they injured in any way. If a group of scientists took my snot and experimented on it for 50 years, I would not expect my descendants to receive compensation.

    Posted by Big Joe on February 1,2010 | 11:34 PM

    This is extraordinary!!! A must buy book for everyone!

    Posted by Robert H. Perez on February 1,2010 | 11:34 PM

    Interesting !!!!

    Posted by tuk srisada on February 1,2010 | 11:34 PM

    PRAISE BE TO ALMIGHTY GOD !!! AFTER ALL THESE YEARS WE HAVE FOUND OUT THAR A BLACK MAN'S CELL IS SAVING THE WORLD!
    MANY WHITES WOULD HAVE PREFERED TO DIE OF POLIO THAN HAVING A BLACK MAN'S CELL INJESCTED INTO THEM LETS SEE IF THE WHITES WILL STOP RECEIVING C=VACCINATION NOW.
    GLORY BE TO JAH.

    Posted by Pius Bito on February 1,2010 | 11:35 PM

    If you just take your "Kids Flintstones Vitamins," you will live forever...I had no idea those vitamins were so powerful, amazing :)

    Posted by Nathaniel on February 1,2010 | 11:35 PM

    I read here that her cervical cancer were from HIV cells floating on dust cells, that she was allowed to die because she was black and not white,that she suffered indignity because of being black and other inane statements that just obscure the writer's, who was even attacked as keeping money and not sharing with Ms. Lack's family, message.
    Cervical cancer is a killer now and was fifty years ago, the researchers at Johns Hopkins, if they were racists, would not use a black woman's cells for ANYTHING.
    Did any of you non thinkers ever think that maybe she was the only young woman with cervical cancer at the hospital and they needed cancer cells. If you READ the article, the researcher hid her identity not because of her color, but because of the press trying to find her family and cell research is anonymous....Go read Popular Mechanics if you can't digest something from Smithsonian without giving it a racial slant.

    Posted by Ed Kosinski on February 1,2010 | 11:35 PM

    From the photo, she was very beautiful. They make a handsome couple. I wonder if she ever knew they had taken and used her tissue for their experiments. Although millions were made off her cells and they knew who she was, why wasn't this money shared with the family? Obviously greed was involved as much as the urge to cure.

    Posted by Ladyredwing on February 1,2010 | 11:35 PM

    This was a great article you learn something new everyday, that lady is an angel. I would love to buy the book to see if the family was given what is there and if the daughter found out all the information she wanted to know about her mom because that crazy plz let me know where can i get this book!!!!!!!!!!!!!!!ASAP thanj you

    Posted by jokesta on February 1,2010 | 11:35 PM

    wowwwwww......this is incredible,are u saying she is super hero?God bless her...

    Posted by samuel on February 1,2010 | 11:36 PM

    I AGREE THE FAMILY SHOULD HAVE BEEN GIVEN SOMETHING FROM THE BEGINNING.I ALSO BELIEVE IF IT WERE A WHITE WOMAN THINGS WOULD BE DIFFERENT.KARMA IS ALIVE AND GOD KNOWS EVERYTHING. IT MAKES ME SAD TO SEE THIS PEOPLE WITH OUT HEALTH CARE, YET THERE BODY WAS USED TO HELP THE HEALTH OF OTHERS. HOW ABOUT GIVING PROPER HEALTH CARE EVEN TODAY TO SAVE LIVES INSTEAD. EVERYTHING DEPENDS ON WHO YOU ARE BUT MANY DENIE THIS. I ALSO DO BELIEVE THE CHILDREN AND GRAND CHILDREN OF THIS WOMAN WILL GROW AND NEVER SUFFER BECAUSE GOD FIXES EVERYTHING. NO I AM NOT BLACK BUT LATINA .

    Posted by lilly santiago on February 1,2010 | 11:36 PM

    After reading this article I sit here in wonderment and the only thought on my mine is that this woman is a descendant Jesus Christ!

    Posted by Anthony W. Logan on February 1,2010 | 11:36 PM

    I'm amazed at how many people saw this as a racial thing. I'm caucasian & recently had a hysterectomy. If scientists could have used my cells in some way that would help others & save lives, I would be thrilled; & I wouldn't want a dime in payment! Helping humanity is something we should all want to do without asking what's in it for me. Thank you, Henrietta.

    Posted by Susan S on February 1,2010 | 11:36 PM

    This book sounds facinating as I am in college to become a Medical Lab Scientist. I am just beginning to understand the use of cells in the lab. Things from how much medicine/antibiotics to use for a patient, to breaththroughs in medicine and cancer victoms, healing our elderly,our children.Etc. There are many scientists out there whose only desires are to study, research, and discover cures for the sake of human life and to give us a better standard of life from their discoveries...Education and hard work should pay off as it has been earned through 8 years or more of hard work,study, and sacrifice! Yes, there are companies/people out there to make money and exploit, it is to be expected. That is why it is important to educate yourselves.Research and know what you are learning about. We now have laws for patient privacy. They didnt back then. You should not apply our rules from our time to things that were done in the past. We as a people, as a human race should learn from our history from our mistakes and wrongdoings and improve with that knowledge!
    And I believe people that think those dr's were only thinking, "oooh lets take her cells to make millions" is a very close minded and ignorant asumption to make. A discovery was made that had never been made before!!!! What a gift from God! Shame on those people that can only see greed, rascimn and malisous intentions! Why can people not see beyond color I wonder? No one looks at discoveries or contributions of a non-black person and says, "oh he or she discovered this and they were Asian or white!" There is still injustice to not only blacks but to children especially, and women. I do believe the initial family should be reimbursed for the discovery though. And a college fund set up for any family members would be a wonderful token of gratitude and rememberence of the research done in Henrietta's name.

    Posted by Heather G. on February 1,2010 | 11:37 PM

    If only Henrietta could have known how important she would be to all human-kind. I find this as fascinating as everyone else and I too will be reading the book. I just have to know more. Now I want to exactly who this woman was and about all of the testing and results. I want to know more about her family as well.

    Posted by Dean Kesler on February 1,2010 | 11:37 PM

    The book is set for released 2/2/10 on Amazon.com. They are taking preorders now. I have just added it to my "wish list". The whole story sounds fascinating!

    Posted by D Walker on February 1,2010 | 11:37 PM

    HeLa's family should be awarded a nobel prize, in honor of her.. great story..

    Posted by Brian on February 1,2010 | 11:37 PM

    Disturbing... a vaccine created from undying tumor cells and in cloning? Couldn't even imagine this up in my nightmares. Science has become so horrible. I just hope nature cleanses us from this world before we become abominations.

    Posted by Nick C on February 1,2010 | 11:37 PM

    This is a excellent piece of reporting. The story is fascinating and leaves a great deal of room for thought. I cannot imagine the emotional ups and downs the family must have experienced. Thank you so much for bringing the truth to the surface. I would love to read the book in its entirety.

    Posted by jeannie ramirez on February 1,2010 | 11:37 PM

    GOOD JOB I WILL BUY THIS BOOK WHEN CAN I GET THE BOOK? YOU SHOULD SEND ONE TO OBAMA. KEEP UP THE GOOD WORK.

    Posted by kev. j s on February 1,2010 | 11:38 PM

    I too have immortal cells.

    Posted by Connor on February 1,2010 | 11:38 PM

    Should make this into a movie. Convey message of Our Humanity & Our Need to save someone's life.

    Posted by Shokelui on February 1,2010 | 11:38 PM

    ohhh.. nice very interesting...I would like to buy the books also :-)

    Posted by Michelle Marzo on February 1,2010 | 11:38 PM

    All things are not as simple as they seem.

    Posted by Kay on February 1,2010 | 11:38 PM

    im 12 and this was very interisting and hard to believe

    Posted by tanya chapman on February 1,2010 | 11:38 PM

    Very Intriqing article. I will be watching for the book. Well written as well, I usually end up getting bored and quiting before the conclusion but you did a good job keeping my interest. Thanks.

    Posted by KD DOWELL on February 1,2010 | 11:38 PM

    Fascinating! And so timely for Black History Month. So many more untold stories like this should be revealed. I'm a visual person as well as a former TV news reporter. This would be a great segment on 60 Minutes and 20/20.

    Posted by Felicia Griffin on February 1,2010 | 11:39 PM

    AMAZING to know this because I previously held a bottle of HeLa cell line without any idea where it came from!

    Posted by kitty on February 1,2010 | 11:39 PM

    it is a cell that is alive.. are we looking at us reach atlist 102 years old.. or just something to think and to write on this article? war is still an issue? pls no war included on this story ok!!! ONE CELL ONE HEART ONE HOME ONE EARTH.. GO HENRIETA.. thank you for the story..

    Posted by bongking on February 1,2010 | 11:40 PM

    Amazing...I wanna buy that book!

    Posted by Myla Quinto on February 1,2010 | 11:41 PM

    Amazing story where they able to map the cells and did the family get compensation. What a good story for Black History month.

    Posted by Ed Robinson on February 1,2010 | 11:41 PM

    If this is true.. it's incredibly amazing!

    Posted by Let on February 1,2010 | 11:42 PM

    The entire story is fascinating. What is, also, interesting are the number of people whose only concern is whether the family got paid or not.

    I won't rest until I read this book. What a journey!

    Posted by Davida L. Day on February 1,2010 | 11:42 PM

    Yes we shiould have cells testing, it may help us fine a cure for all illness, in our life time.
    I think th govenorment should set a side money to help with the cells testing.

    Posted by jacqueline on February 1,2010 | 11:43 PM

    Careful write up!, ‘It consumed their lives in that way’ means no compensation nor acknowledgement that Henrietta was used as a Guinea Pig..No one will ever get compensation for in directory contribution or else medical/scientific litigation will never stop.

    Posted by Ikechukwu on February 1,2010 | 11:43 PM

    It is so interesting... I really enjoy it!!

    Posted by Nina on February 1,2010 | 11:43 PM

    The story of Mrs. Lack was eloquently and poignantly told in Mrs. Henrietta Washington's (should be) seminal book, Medical Apartheid, published in 2006. There is a long history of the use of African-Americans as medical guinea pigs, regardless of the spin given to Mrs. Lacks' "contribution".

    If you want to read about Mrs. Lacks, who at some point resided in Turner Station in Baltimore, Maryland, in a larger context, read Ms. Washington's book. There are several articles about her that predate the 1990's. "The cells that would not die", The Baltimore Sun, March 1981. "The immortal cells of Henrietta Lacks", Reader's Digest, September 1986. Another article, "Her cells made her immortal", The Baltimore Sun, March 1997, and a more recent article (not cited) written perhaps in 2005, also express the sentiments of her family.

    Posted by Jan on February 1,2010 | 11:44 PM

    Scientists are human too,they must realise the importance of other human being's body parts.cells utilised illegally just for the sake of money...This is all signs of Almighty God for the humans to know and understand who is their creater.
    On one scientific invention,scientists are appreciated so much and gets recognition all over the world.What about God who created you from a single pair..Have you ever given a thought about it...What you are doing is right or wrong?
    Have anybody ever thought what would have happened to Henrietta after her death..

    Posted by Roz on February 1,2010 | 11:44 PM

    How does one know she really had cancer got to read this book.

    Posted by Shay on February 1,2010 | 11:44 PM

    This is both interesting and bittersweet. Especially during Black History Month. I just wrote about Black inventors for my website. Many could not get patents until after the Civil War. One inventor sold his invention - just to buy his freedom. This makes me think about how race does matter, education does matter, and humanity matters. Also reminds me of the Tuskegee study, and how poor, illiterate blacks were given syphillus, unknowingly. The price we pay for healing - our bodies and our nation is big. And bittersweet.

    Posted by CJazz on February 1,2010 | 11:44 PM

    Thank you Henrietta.

    Posted by Phil on February 1,2010 | 11:44 PM

    The origin of stem cell research!!! How amazing!! Can't wait to read the book..

    Posted by Tami on February 1,2010 | 11:45 PM

    Almost all cancer cells are immortal (relative to the rest)... it is true that scientists don't know why, but that doesn't mean that her cells are anything remarkably different than the rest of ours.

    Posted by Jeff on February 1,2010 | 11:45 PM

    Incredible... the sons are after the money.... instead of getting an education and working hard... gotta get their piece of the pie....

    pathetic

    Posted by fred on February 1,2010 | 11:46 PM

    WOW!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!

    Posted by maurice thrower on February 1,2010 | 11:46 PM

    real super hero lives among us.....like me,can anyone ever believe someone can fly?believe or not...thank u hela....

    Posted by samuel on February 1,2010 | 11:46 PM

    I have mixed feelings about this story. Ethnic issues asside, it bothers me that a persons tissue samaples can be sent somewhere and manipulated, without the permision of that person. OK maybe in the time frame it happened, science was that new, that no one knew any diff., still bothers me that a part of me can be used for scientific study because I don't totally agree with all areas of thier sientific study, so I should be consulted first.

    Posted by PJ on February 1,2010 | 11:46 PM

    This is an amazing story. I thought this only happen in movies. I'd just like to be clarified, does this mean that the cell of Henrietta Lack is immortal?If so, how come that Lack still died?Is there any possibility in this world that a human being can really be immortal? This is so intriguing.. I want to have a copy of the book.

    Posted by Mhy on February 1,2010 | 11:47 PM

    how do we they didnt start spreading more cancer that way

    Posted by jimmy on February 1,2010 | 11:47 PM

    I am eleven years old and even I think this writting is interesting!!! But it's a little scary.

    Posted by Megan on February 1,2010 | 11:48 PM

    Very interesting would like to know more about it.

    Posted by Abreu on February 1,2010 | 11:48 PM

    this story is amazing,

    Posted by katherine dela cruz on February 1,2010 | 11:49 PM

    Race matters, being that it was 1951 when this all took place. So if you are not black and saying that you should just think about how whites did evil things to the black race back then. Not all, but alot. Yes the family should get money that is rightfully theirs. It does not matter if they did not care about the cells or if they did not want to participate in donating their own. They had the right to be given the money along time ago. Yes black history should be taught in schools because black history is not taught enough in certain areas of our country.

    Posted by J on February 1,2010 | 11:49 PM

    It's very hard for me to believe but if it is true,ok it's amazing. But only God can understand it fully.

    Posted by jim on February 1,2010 | 11:49 PM

    It's very interesting.

    Posted by S.S. on February 1,2010 | 11:49 PM

    Great journalism! Credit to the biology teacher as well,I hope his or her name is or will be mentioned somewhere! As for the Lacks, I believe a NOBEL prize award in the area of "Sustainable Development "is befitting as a great source to improving our humanity.

    Posted by Tebogo Motswai on February 1,2010 | 11:50 PM

    This story is remarkable,Thanks Henrietta Lacks and its family.Afoundation need to be made on behalf of(HELLA CELLS) for as longas itlive or use for menkind.I'W be looking for the Book!!
    Thanks(Rebecca Skloot) for the remarkable story. From FJ.

    Posted by Fermin Jeff on February 1,2010 | 11:50 PM

    Nice article. BTW, is it just me or does anyone else think that Henrietta resemble ABC's Robin Roberts?

    Posted by Judi Pennella on February 1,2010 | 11:50 PM

    This is an amazing story. I am so glad I ran across this. I plan to buy the book tomorrow on my lunch break. The O Magazine ran part of the story in the February issue. I was able to read 5000 words of the book online. Now I can't wait to read the entire book. I am so glad Ms. Skloot researched this story and wrote this book. She should win some sort of an award for this. Excellent!

    Posted by Paulene on February 1,2010 | 11:51 PM

    I think this woman's family of relatives should be presented with some tpe of posthumous award in her honor.

    Posted by bert trandel on February 1,2010 | 11:51 PM

    I would like to donate some sperm cells. My genes are off the chart!

    Posted by kev on February 1,2010 | 11:51 PM

    "Valtava" Great
    Good to know about Hela cell in first begin step in biological, some people never die in our mind and thoughts is this is the most likely person Hela to landmark for new students. Just i can say to be happy to hela family members that they had got legend lady.

    Posted by Tameem Saudagar on February 1,2010 | 11:51 PM

    Wow, great ready...love the story behind the cell. Who knew!

    Posted by huggins on February 1,2010 | 11:51 PM

    What a wonderful piece, and BRAVO! For the quality in which it is written and published on this very first day of Black History Month, 2010. I am on a fixed income so I could not spend a lot on presents for Christmas, 2009, but I bought what I felt was one special affordable present to give to my daughter and her husband who are expecting their first child in June this year. I gave them one of those ole large, Family Bibles like the ones we use to record special dates in back in the day. They were very happy to get the bible. Little did I know that they were thinking like me. They gifted me with a membership to Ancestry.com. I have been diligently seeking information for them and recording it. After saying all that, I mostly want to also say that we should share as much of our history with our children and other family members. It has really been hard to trace back especially since my parents, aunts, uncles, sisters and brothers have all pasted on. Only one left out of 8 and me. Also, I told my daughter and son in law that I am Willing my body to Medical Science, at Mayo Clinic in Rochester, Minnesota. This decision was made after my study about Plastination and organ donations. I cannot think of a better way to leave a legacy.
    Save a life, please consider being an organ doner.

    Posted by Jeanette Hill-Resnick on February 1,2010 | 11:51 PM

    amazing...sounds unusual and interesting.A must read book.

    Posted by shals on February 1,2010 | 11:51 PM

    yes facinating sure. Should she be paid for her cells that is just silly. I don't know how they become immortal. You don't take a dump and say those are my cells in there somewhere and I should be paid for it if there is any gold cells in there. Cancer seems to be stronger than anyone and usually is cause of some dealths. So we are cells but people are a combination of cells. Not what they capture or how their body responds to them. I guess that might be some DNA or some environmental external or as we are all connected biochemically. Can't ignore the fact there are many microscopic things living around us and some of those things are so strong they could kill you. I don't know what to make of it. Great to see much progress was made and discovered but doesn't sound like there is a reason for these cells living. The heck with the story about a woman who got sick. How about the science behind it. That is the interesting part. The woman who had this makeup or disease is not that interesting. To find out someone is sick is not no happy ending. People kind of benefiting from it is kind of a happy ending. To take cells happens all the time in samples (biopseys?). You would like to know if someone is using them for something but they are not really exactly yours. Life is only temporary until something fails and you can no longer live or disease takes over. You need all systems as functioning not just one cell or one type of cell.

    Posted by George washington on February 1,2010 | 11:51 PM

    This was a very interesting article. I would be very interested to read the book too.

    Posted by Elizabeth Delzer on February 1,2010 | 11:51 PM

    Why do these storys happen to come out on black history month

    Posted by jimmy on February 1,2010 | 11:52 PM

    That Henrietta's family doesn't have health care when their Mother is source of Medicine is terrible. I imagine if they had been given any money at all, it would have been in this report. To the author, excellent writing. Thank you for your persistence.

    Posted by Karen Martino on February 1,2010 | 11:52 PM

    I would like to start by saying this is a very fascinating,and very interesting article! but why is it so fascinating that it came from a black woman,DNA is DNA.Let's look at the time frame this all took place over 50 years ago! things were different the FDA didn't have the rules and regulations that they have today. I really feel the doctor or doctors, hearts were in the right place trying to find cures for these horrible diseases.Henrietta Lacks cells where truly one of a kind that helped millions of people of all race. I can almost bet her family would not have allowed her cells to be donated to science.All though i admit there was some sneakyness involved,look at all the good that has come out of this poor woman's tragady!the help in developing polio,vitro fertilization.and many more.There are people today that donate tissue,organs,cells,eyes just so people can live.Deborahs brothers weren't the least bit interested in there mothers death until they heard they could profit!!!Shame on them they should be proud there mother made history and brought comfort to so many people.As far as them making millions, it takes millions to find cures!!

    Posted by Jamie Champ on February 1,2010 | 11:52 PM

    This is really Amazing but we have to remeber that; God has a reason for everything. Scientist must agree, confess and believe that God created everything including themselves and give them courage and use their brain to help others from their discoveries. The scientist must think of how the Family of Henrietta is gaining profit from their mother's, and Grand Ma's Cell donation.

    Posted by Lucky on February 1,2010 | 11:52 PM

    To Nancy Salisbury: You posted a comment today about your grandfather and your relation to the family of Daniel Boone, but you did not leave a contact, or at least none was posted. I wanted to let you know that you might find information at the Kentucky Gateway Museum Center in Maysville, Kentucky. I'm not sure what they'll be able to help you with, but it's worth a shot. There is history here in Maysville regarding Daniel Boone, and even an old cemetery behind the museum center that I believe has some of his family (maybe a brother?) buried there. Also, check museum and library resources in Lexington, Kentucky for Henry Clay. There is a "Henry Clay House", if your grandfather was any relation (given his name), as he was a prominent part of Lexington's and Kentucky's history. I hope this helps you out! Please don't hesitate to contact me if you would like to speak about it. 606-564-6815 -Matt

    Posted by Matt Bays on February 1,2010 | 11:52 PM

    When you think of how many lives have been saved and the impact these cells have made ,and are still making, it is sad that Mrs. Lacks children, some who were too young when their mother died to have known her, are without health care, and have no inheritance. Her DNA although extremely useful was stolen. It seems they are still looking to the family for more exploits. They should be compensated.

    Posted by Feisfocused on February 1,2010 | 11:52 PM

    Again, compensation. Again, "her contribution". The value of the cell line came from the development of those cells. By themselves, cells have no value beyond dust mite food! And those cells at the time were no more than waste. This is like saying the guy who threw away the orange that penicillium mold was discovered growing on deserves billions of dollars because of penicillin! How utterly absurb!

    As to her "contribution", she made none. Contribute is an act. She did nothing. She did not answer an ad somewhere and selfless go down to the hospital and agree to go through an invasive process to cull those cells. She contributed zero.

    Posted by Michael Honohan on February 1,2010 | 11:53 PM

    This must be a real good story, like 50 years in the making? I hope someday this can make its way to a film. I like the way the article was narrated, the build-up of emotions is great. Made me more interested and mystified with this subject.

    Posted by ben on February 1,2010 | 11:53 PM

    I think this is an amazing story.......however the scientist were wrong how they went about getting her cell dishonestly.
    But regardless all I see any more is all about money money money and that is all people really think about... this woman is a part of History she and many others have suffered and went through many things and I am sure if she thought her cells would help cure disease she would be very happy.

    Posted by Debra on February 1,2010 | 11:53 PM

    Such an amazing article!!!

    Posted by irene tey on February 1,2010 | 11:53 PM

    I hope that the family get some copinsation from this. Why wern't they told sooner about it?. 1951 until now, amazing and unbelievable that it was kept away from them for so long.

    Posted by terry on February 1,2010 | 11:54 PM

    But why should a doctor took a sample from a partient without any notification? and why despite the abundant wealth generated through the research the woman and her family were allow to die miserably in poverty? This to me is a disrespect to human life and abuse to mankind in general.

    Posted by mohammed yusuf on February 1,2010 | 11:54 PM

    A well written article and intices one to learn more! The author's care and concern shown in her approaches to the Lacks family is remarkable in this age of sensationalistic journalism. Ms. Skloot's did exercise great tact and sensitivity and shows great skill in telling the history that needs to be well known beyond the average scientist.

    Fitting to be in time for black history month. I hope this inspiring story encourages many young people to enter into the sciences rather than become lawyers! JUST THINK of the good that could been done with more brain power devoted to helping all of humankind with scientific break-throughs.

    While the 1950s had some or a lot of different business and ethics practices, it simply was a different era in respecting anyone's body (whether white,red, yellow or brown) for scientific use. THIS WAS OVER 60 YEARS AGO!!! Maybe not an excuse, but that was the sad case back then.

    So fast forward to this millenium...we Americans have evolved and been graced by HeLa's cells and those results. We should all be so very pround of Henrietta's contributions. In fact, anyone can contribute and be the one person that makes a difference. DARE TO BE AN ORGAN DONOR. I am.

    I also always knowingly and with informed consent donate my tissues/cells to research after any surgeries/procedures. In short, I can't use them any longer personally, so I always hope science can do something beneficial for at least one other human. Why not help someone else out? I'd be honored if I was able to help out just one person and make a positive difference.

    Posted by Jane Allerton on February 1,2010 | 11:54 PM

    WOW!!!!This is so so amazing to hear.I am so proud to be African American, this book such be in school all over the world this is very educational it make me read more about History of black cell.the scientist who did this know Mrs Henrietta Lacks and know she was BLACK WOMAN ,and they know of her family and did not help them so!so!so in human thank you for my black History, the truth is coming out and WHAT NEXT? are WHO NEXT?**GOD DON"T MAKE ANY MISTAKE************
    ********BLESS YOU MRS. Henrietta Lacks and your family********

    Posted by Gloria Mccarey-Tate on February 1,2010 | 11:54 PM

    WOW!! This was an amazing piece of writing. It could have been something out of a sci-fi magazine or movie on TV back in the 1950's. What scientific breakthroughs were going on way back then and it wasn't even known to the majority of the public, what a shame. I was one of the recipientes of the first polio vaccine back in the '50's and to think all these years I had no idea that it was due to a black woman's cells, how interesting considering I was born and raised in the south with segregation all around me until I was an adult. I wonder if folks would have known how that vaccine was made, from a black woman's cells, if there would have been any backlash over giving that polio vaccine??? Maybe that is one reason scientist didn't let the public know, just food for thought!! Reading this makes me want to buy the book and find out more about the family.

    Posted by Cindy on February 1,2010 | 11:54 PM

    I don't see a problem with cell lines so long as permission is asked. I'd also most certainly not want to see patents for genes coming out of donated material. Want a big $$$ patent pay the patient royalties. Better outlaw patents on genetic material, we didn't create these genes, we discovered them. Astronomers don't get to patent stars, nor geologist rocks, why does big pharma get to patent genes?

    Posted by Larry on February 1,2010 | 11:54 PM

    is this true? it's like a story froman anime or something

    Posted by sielre on February 1,2010 | 11:55 PM

    Wow, that story is truly touching and the fact that it's from a black women, ties together perfectly for Black History Month.

    great job!

    Posted by rose on February 1,2010 | 11:55 PM

    Very intriguing.

    Posted by Arman Muleem on February 1,2010 | 11:55 PM

    I saw this on the 60 minutes. This is an amazing story, but at the same time the scientist was wrong for not asking her could he take her cell and do research with it. The family needs something out of this.

    Posted by Traci R. on February 1,2010 | 11:55 PM

    This is a wonderful story. Somewhere, somehow God's creation has left a footprint for medical research. Compansating the Family would be a wise thing to do. Also, Henrietta's family should first give thanks to the almighty and most powerful God, then to the research community for the great work they have done.

    Posted by Elaine on February 1,2010 | 11:55 PM

    WoW! this is a amazing story I worked with the HELA Cells myself at a university I attended last fall Nad I never knew that she was a black woman nor did I know that her family was suffering in various ways because of this issue about her cells. I am definately going to but this book!

    Posted by Ebonique M on February 1,2010 | 11:55 PM

    I'm reading this book. It is so well written and researched. I'm appalled at how this poor women went through and how she was treated.

    Posted by Carol Gerwitz on February 1,2010 | 11:55 PM

    Wow that is amazing! It truly is awesome some of the things that scientists can do. I think that H. Lacks's family should be proud of their mother! I'm sure that she helped save alot of lives. I do agree that they should have some compensation because good grief they've made alot of money off of it. They could spare at least enough to get the family out of poverty. Instead of compensation, they could just call it a donation.

    Posted by Tia on February 1,2010 | 11:55 PM

    This immediately caught my attention because HeLa cells were discussed in my molecular cell biology class last week. the instructor showd a picture of HeLa but I couldn't tell that she was black. Interesting. I might buy this book. Good article.

    Posted by zach on February 1,2010 | 11:55 PM

    This is a fascinating piece that will help shield light on some scientific mysteries that ordinary people out of the scientific domain cannot understand in medicine. thanks for sharing this brillant isuues. I can't wait to read the whole story.

    Posted by David on February 1,2010 | 11:56 PM

    MY, MY, MY, WHAT DO WE HAVE HERE? WE FINALLY HAVE THE TRUTH ABOUT WHAT REALLY HAPPENED IN 1951. THIS GOES BACK EVEN FURTHER THAN THAT IF BLACK PEOPLE TAKE THE TIME TO LEARN THIER HISTORY THEY WILL SEE THAT THE AFRICAN RACE IS THE MOST DOMINANT OF THE RACES AND TRULY EQUIPPED TO HAVE CELLS THAT CAN LIVE AND PRODUCE IN THIS MANNER. GO BACK EVEN FURTHER TO THE CAUCAUS MOUNTAINS AND LEARN WHY INDIVIDUALS HAD TO MIGRATE THERE? BECAUSE THEY COULDN'T MAKE IT IN EGYPT. A LITTLE FOOD FOR THOUGHT. GO RESEARCH GO FIGURE!!!!!!

    Posted by ALICIA BLAKELY on February 1,2010 | 11:56 PM

    I find it sad that many of the comments lead back to race and money.
    It never fails to make me shake my head in wonder when people who want "equality" immediately point out the word "black" and the different races involved in any article such as this. Why is it a big deal whether she is African American or white? Focusing on that stereotype (she was black, so they used her) simply prolongs any sort of separation there might be between races. For a country that wants no division, we seem very determined to create one.

    Money-wise, it doesn't seem as though the family should get any compensation. It sounds just like a bunch of greedy people trying to milk the system because they realized all of the sudden that it might be possible for them to do so. Anyone else who contributed to science didn't receive any sort of "compensation" for their heirs, they did it to advance human society. This case might be a little different because it was taken without the woman knowing, but either way, the cells didn't belong to the kids, they belonged to Henrietta Lacks. There's no claim to money from the children. I will add that I do think it is despicable that the medical field profited monetarily from their usage as well.

    Posted by Meaghan on February 1,2010 | 11:57 PM

    Amazing and very interesting.... her immediate family should be conpensated

    Posted by M. J. Cabansag on February 1,2010 | 11:57 PM

    For those who have made comments that this family should not seek compensation from whoever was resposible for stealing this woman's cell are full of it. What that doctor did by taking this woman's cells was wrong and as I was reading this article I was shocked to find out that the family had not pressed charges or sued yet. It was wrong for that doctor to do that and I think the family should be compensated in some kind of way. I know why her cells were taken and nothing was done about it, but that's to be discussed in another forum.

    Posted by uknowme on February 1,2010 | 11:58 PM

    Amazing! I will definitely buy the book. I thank my daughter for sending me the article!

    Posted by GAlbert on February 1,2010 | 11:58 PM

    To all of you read the book "Medical Apartheid - The Dark History of Medical Experimentation on Black Americans from Colonial Times to the Present" by Harriet A. Washington. Civil Rights Leader Fannie Lou Hamer was subjected to a "Mississippi appendectomy" - a nonconsensual sterilization-to which she ascribed her political awakening. Black people have never had any rights even over their own bodies. So, a White doctor would have every right to take whatever he needed and didn't have to ask.

    Posted by ava on February 1,2010 | 11:58 PM

    Interesting story. I had never heard of cells living a long time like this. And to think of the huge health benefits that arise from long lasting cells stuns me. Think of the millions or even billions of lives these and other cells will save.

    Kandi made me laugh with her post. Good humor. But I doubt anyone will get anything monetary out of these cells other than medical research. And I don't think they should receive anything.

    The Dr that took them did so in the tiny hope of furthering his fellow scientists along the way. He probably thought nothing of it in that day and age. And he surely never even imagined the great boost in cures from this one small piece of tumor. Cells were taken from hundreds of thousands of unknowing people back then. Just because Mrs Lacks cells proved very helpful does not mean big "money". The HUGE honor of her name on these cells is enough.

    It's a good thing cells are anonymous now. "Give me money, I deserve money, Are you going to pay me money, You owe me money, I'll sue you for more money, I get a percentage of fill-in-the-blank." How ugly money hungry. Gag!! Medical research would practically come to a standstill and fewer cures would be found.

    Posted by Thinking on it on February 1,2010 | 11:58 PM

    Yes good story, well written until the end. I still wanna know what happend to all that money after the ending of that movie with the crazed killer being the star???

    Posted by Dee Perre on February 1,2010 | 11:59 PM

    I read about this in Oprah's magazine, and I was appalled. The fact that she was not told what was being done with her cells and that people have profitted while her family continues to live in poverty is why people of color have a valid reason to mistrust doctors. Her family should receive a large portion of any money that has been earned and an apology.

    Posted by Lisa on February 1,2010 | 11:59 PM

    wow really interesting. I may just go and get the book. I find this very very interesting

    Posted by Heather on February 1,2010 | 11:59 PM

    I took a genetics class in college 15 years ago that revolved around growing these cells all quarter. All we were told was that they were cervical cells originating from a woman in the 50's. Their growth started out normally and they became increasingly multinucleated as time progressed. I've never been able to forget it. For something so personal from this family to be shared with the world for the sake of science is commendable, but for it to be taken from them without their knowledge and just compensation or even an apology is just deplorable.

    Posted by RB on February 1,2010 | 11:59 PM

    I disagree with the person(s) that stated if Henrietta was a white woman-she would have been known about years ago. Many donors for research purposes or otherwise often are anonymous, or unnamed due to age old laws reguarding Doctor/patient priveledge (confidentiality), known today as hippa laws. I am amazed by this story for that reason, you never hear about the people that helped us get where we are today in medical advances-simply from being a donor. Truly amazing! Thank You Henrietta:)

    Posted by Michelle b on February 1,2010 | 11:59 PM

    wow! its interesting to know.

    Posted by Engr. Ataul on February 1,2010 | 11:59 PM

    A wonderful and very timely revelation. I am very excited to find out if there are other individuals who are gifted with "immortal cells".

    Posted by Orlando Racelis on February 1,2010 | 11:59 PM

    Fascinating! And I do totally agree with the suggestion that her Family should be given some sort of financial compensation. They are truly in need of financial assistance and she was not asked for her permission to use her cells in this way. She may or may not have agreed. That is why, her family and generations should be compensated for this , long term.

    Posted by dawkhinmaytun on February 1,2010 | 12:00 AM

    YES. An amazing story. And I will buy the book. And I do hope that Ms.Lacks family receives royalities from the book sales. BUT here's my question: So many of the comments are about RACE? Why? Why can't we just get past the part of race and simply recognize we're all human beings. The color of our skins are surely noticeable and I wouldn't want a world where everyone was the same....but could someone please explain to me why EVERYTHING seems to revolve around RACE.

    Posted by Eva P on February 1,2010 | 12:00 AM

    It's great that Henrietta Lack's cells have resulted in so many wonderful discoveries. But, lots of people, most of them white males, have made billions of dollars and built successful careers off of her body. The family should be duly compensated. Its immoral and should be illegal that the cells were taken and used without Mrs. Lack's permission. The insult is doubled that her family was never told. I wonder how many people would be willing to let bygones be bygones without compensation if it were their mother, grandmother or sister. Unfortunately, this is another example of abuse of a poor, uneducated person by rich, powerful institutions.

    Posted by Shirley D on February 1,2010 | 12:00 AM

    How about the family? They must be compensated for the sale of their mothers "immortal cell". interesting!

    Posted by Julius Francis on February 1,2010 | 12:00 AM

    I grow up not too far Clover Va Those White Doctors in that area just used uneducated Black people. I thought they just took our land and houses if we couldn't pay them but Wow our DNA too.

    Posted by Belinda on February 1,2010 | 12:00 AM

    As the cells were originally taken from the tumor why would anyone become angry at the researcher for taking them, the tumor would have just gone into medical waste and incinerated. Unfortunately thats the problem with society here in the USA, it's all about the money. Why cannot they just be pleased that their heritage has contributed to medical advances. I'd be proud of that.

    Great research for a book , I found it an interesting article.

    Posted by tb on February 1,2010 | 12:00 AM

    very interesting,it makes you think,does anyone know the name of the book?

    Posted by LAURA on February 1,2010 | 12:00 AM

    A great story! Can't wait to read the book. Ethics should have dictated if this family should have been advised of the great contibution their mother had made; so many lives saved. I am sure Polio was not the only disease that was controlled by immunization. Even that knowledge would have made a difference to her children, who had to grow up without a mother. God Bless You Henrietta Lacks!

    Posted by Kate on February 1,2010 | 12:01 AM

    I think that this was and is a great story. The fact that this is a true story makes it real. I think the family should be compensated in some way from this MOTHER'S LIVING CELLS. I WANT TO READ THE BOOK. I WANT TO THANK MRS lACK AND HER FAILY FOR THE SACRAFICE MADE. I REMEMBER THE SPRING DAY THAT I TOOK THE POLIO SHOT IN 1957 AND REMEMBER THAT ALL OF MY CLASSMATES REMEMBER VERY WELL TOO. WE WERE ALL GLAD TO BE PROTECTED AGAINST THE DREADED POLIO. STILL ARE.
    You know,someone mentioned the idea of exhuming Henrietta's body to see if it has continued in tact. This is not a morbid idea. The idea here is that It brings a hint of Hope. It is a small peek at God. This is a sacred act. Any such act should be treated in a sacred and respectful way. This is Not for money or greed's sake. Not at all. But with full permission and only with full permission of the surviving near real blood relatives consent. And if it be nay, then, as Jesus said, "...let your answer be either yea, yea or nay, nay. For whatsoever cometh to more than this, is evil." Matt. 5:37. But only the family should say.

    Thank you again Mrs Henrietta Lack

    Posted by DAVID GUY on February 1,2010 | 12:01 AM

    There are four important facts that matter in this story. 1. There was no law dictating how these things should be dealt with at the time. In fact, there were likely hundreds or thousands of people at the time whos tissues were used in some way that was not related to their treatment or diagnosis. 2. Today, it happens every day. People sign consent forms for surgery and that gives the hospital rights to do with their "samples" as they see fit and as is approved by an internal review board irrespective of the person, their race, ethnic background socioeconomic status etc., 3. Henrietta probably helped more people and saved more lives than any other african american on the planet. 4. Whether you are a conspiracy theorist or not, there are laws that I personally have had to deal with that strictly prohibit the profit from the sale of human tissue. If we were talking about some third world country here it would be a different story. As a person who is deeply involved in the medico-scientific arena, I think Henrietta Deserves more than a couple million dollars to her heirs. I think SHE deserves a national holiday. Anyone who DOESN'T have Polio, cervical cancer, or who has survived ANY kind of cancer as a result of modern medicine's intervention, should lead that charge.

    Posted by Science boy on February 1,2010 | 12:01 AM

    May be Mrs. Henrietta mind her cells remaining alive to better mankind,and also,her offspring

    Posted by wattwheel on February 1,2010 | 12:01 AM

    I don't buy the racism thing. There were probably plenty of "white folk" that ended up being guinea pigs in the 50's and even today. Come on ladies, of all races! What did that black or white or Asian or "Native American" doctor do with your cells the last time you got a PAP Smear? Did he/she promise to not keep any cells for himself/herself?

    It has nothing to do with race! And, why should anyone be compensated for something that was done to their ancestors.

    No handouts. Do the right thing!

    Posted by ken on February 1,2010 | 12:01 AM

    Did the author offer any monies made from the sale of this book to the families involved?

    Posted by Susan Jackson on February 1,2010 | 12:02 AM

    This is what an actual journalistic piece is. Refreshing to read about Henrietta instead of Brangelina.

    Posted by Nicole on February 1,2010 | 12:02 AM

    Interesting!!! I never waste money to buy any book other than what Uni need me to buy but I ll definitely buy this one.

    Posted by Rachel .W on February 1,2010 | 12:02 AM

    That was interesting! Though not conclusive of what ever happened to Henrietta's children particularly their cause to have their "share" of the benefits, money, etc out of their mother's so called helpful and instrumental "immortal cells".

    Posted by Jose Aboniawan on February 1,2010 | 12:02 AM

    Amazing, Imagine all the young people who could be educated and follow up, but the costs are prohibitive to so many of our young people who would love the opportunity, with abilities to make new discoveries and work miracles for mankind.God Bless America, the new day will come.

    Posted by stephanie on February 1,2010 | 12:03 AM

    Interesting story. I can understand the family feeling 'cheated' but they really weren't. She died of cancer. Period. The cells are only part of her remains, not the entire woman. They couldn't live with her cells, talk to them, love them and interact with them. No they weren't cheated but the world did learn from their mother. Too bad they don't understand that.

    Posted by Joyce on February 1,2010 | 12:03 AM

    I really enjoyed this story. Despite some people's criticism of its contents, it does bring certain questions to the table that others may not have considered, even me! To the person who was concerned with the financial motive of some relatives, consider that they are (presumably) as well educated as yourself. People are quite alike in most cultures and a venue for 'getting rich' or even merely getting ahead is not exclusive to any country, based on my observations. I don't necessarily agree with that route, but can at least empathize on their plight. I thought the author made a good summary statement of her outlook on the picture and I thank her for sharing this interesting story. DS

    Posted by David 'Stawasz on February 1,2010 | 12:03 AM

    Once again, this shows that African-Americans and Africans are the center piece to the human race, along with discoveries in Africa, that further prove these facts. Our ancestors come from some of the oldest civilizations known to man, that still exist to this day (Sudan, Somalia,etc.), which further proves our durability and strenght given to us by the ALMIGHTY!!!!! The TRUTH shall set you free. And, it is these truths, that not only we know, but the rest of the world knows, that are continually proven everyday. Eventhough, like the young lady said, the real story is much more subtle and complicated than that, my friends.

    Posted by James Nelson on February 1,2010 | 12:03 AM

    Good stuff! This proves that people really did at one time live to be 100's and even 1,000's of years old according to the bible. Perhaps we are finally catching up to science as it use to be, or is it that there really is nothing new under the son? Thanks to her cells we are able to treat terminal illnesses better than without? If we defeat terminal illnesses, we can conquer death. Aergo, death is an illness that needs to be sqaushed!

    Posted by Tim Jackson on February 1,2010 | 12:04 AM

    I too am very intrigued to read this story.... But I must say the yahoo headline of this woman being a poor tobacco farmer is not accurate! She is in a fur and her Husband is in a suit.... I'm sorry poor people did not wear those types of clothes or have there pictures taken in portriat forms back then. Don't get me wrong, this family were hard working farmers, but they worked just as hard as the rest of us.

    Posted by Mrsbigslow on February 1,2010 | 12:04 AM

    Wait a minute, what you think the medical information disclosure procedure is about?

    Beyond authorizing the medical personels to proceed with the information on one's behalf, such a leverage does not prevent them from doing evil to us... Medical practice is not only a scientific practice, it entails some morality, a lot of ethics unfortunately most scientists are not equipped with...

    Unchecked things of this nature undermine the trust that should engulf us when entering a medical facility... as a patient, do not put yourself in a position of weakness enough not to exercise your right to know about information pertaining to your health status and anything taken off You as part of the medical procedure... Ask and follow up on such lab works... have witnesses about what is being done under you...

    You may not know the practices but malpractices and associated evil conducts are foreseeable... Use your wits!!!

    I do believe that anything taken out of context for the purpose of material exploitation will never end up accordingly with one's evil plans... nature has a Unique way of claiming back what belongs to IT... timelessly so far!

    Demba.

    Posted by DEMBA on February 1,2010 | 12:04 AM

    impressive! life indeed is eternal.

    Posted by Chi Icalla on February 1,2010 | 12:04 AM

    It is a very nice and interesting story. I will share this to my friends..thank u!!!

    Posted by maverick licerio on February 1,2010 | 12:05 AM

    Money!Money! - All the work starts with help to mankind, then once it clicks - people start thinking ways to profit themselves - the last path is write a book and make some noise and say its for the people to know - In the end its money. Mankind @ its lowest.

    Posted by varun on February 1,2010 | 12:05 AM

    Black Don't Crack

    That's funny because I was thinking that before i even opened the link.

    Posted by Cam on February 1,2010 | 12:05 AM

    Wow, What a story! I wanted more!

    Posted by newsie2000 on February 1,2010 | 12:06 AM

    What do you consider as being alive? Are trees alive? Cells could live just like a tree. The soul, now that's where your alive is, and it has gone on.

    Posted by Lisa on February 1,2010 | 12:06 AM

    That is absolutely the most fascinating article I have read in years. It's like the cross-over point between science fiction and reality. And I love the way you left the readers wanting more . Great reporting. I plan on buying the book.

    Posted by mark on February 1,2010 | 12:06 AM

    Her cells are immortal in that they do not experience telomere degradation. Telomeres are the coatings on the ends of strands of chromosomal DNA that tells the cell where to start and stop in the replication process... rather like the aglets (little plastic bits) on the ends of shoelaces. As time goes by, telomeres normally break down and the cell no longer replicates itself normally, bits from one chromosome may drift over to another or break off all together, resulting in a daughter cell with errors in its code. When enough cells in an organism are no longer fucntional, the organism dies because its systems wear down and no longer function properly and dead cells are not repalced with new healthy cells... this normally happens after a set number of replications known as the Hayflick limit.

    Her cells do not express a Hayflick limit. This is why they're so perfect for research, they reproduce exact copies of themselves so long as they are given adequate nutrients to reproduce. One cell divides into two perfect copies, two into four, four into eight.... and so on, all exactly like their parent cell. Since they're all identical, they're perfect for double-blind testing because there is no genetic variable in the samples.

    Research is going on into how to replicate this effect, the lack of telomere degradation and suppression of the Hayflick limit. It opens up the potential for incredible advances in regenerative medicine.

    Posted by Maltheos on February 1,2010 | 12:06 AM

    It's a very interesting story. However, in regards to the compensation issue, are there any logical or rational people left in this world? The money seems to be the common theme of 90% of the comments here. Do you think she was the only person to involuntarily contribute to science? Because her cells contained scientific value her family (50 years later) should receive a cut? Who exactly should be told to pay out this sum of money to the deserving great grandkids? I am not knowledgable enough, nor did I live through the time of the Vietnam war, so who am I to say whether it was just or unjust. But I do know that men were drafted, forced to fight and die for the country and received little more than a thank you. Their lives were taken. Henrietta's skin cells were taken. Let's start to embrace common sense again in this country.

    Posted by Tony on February 1,2010 | 12:06 AM

    What more can I say...they'e said it all. Very enteresting.

    Posted by Tara on February 1,2010 | 12:06 AM

    God's miraculous wonders. Please compensate the family.

    Posted by sally leonado on February 1,2010 | 12:07 AM

    This is an interesting article. Worth the read.

    Posted by Pinay on February 1,2010 | 12:07 AM

    This is a very nice article and I am interested about reading more. As far as the family being compensated I believe that they should be, if people are making money on her cells and she is not alive to recieve any money or benfits from it they should. Just because they are poor and black does not mean they are not entitled to any money. If it was Paris Hilton or one of the rich white people who get or have gotten money through their parents it would be ok. But sense they are black it is wrong I dont think so. We are entitled to things to. And as for her cells helping people and you who are commenting they should be proud of that and keep it moving you try being poor while people are making money off your family and see if you are ok with it. This has been going on forever the indians got their money were is our 40 acres and a mule. We supposed to lay down and just take it. They should try to sue, start with who took and sold the cells in the first place.

    Posted by Queen on February 1,2010 | 12:07 AM

    will the compensate the family? can they do anything about this injustice? totally not fair.

    Posted by queen b on February 1,2010 | 12:07 AM

    very interesting--I do wonder if the family got a share of any profits that have accrued over the years. They (one Dr.) took tissue from HeLa's cancerous tumor, without the know- ledge of any of her family members. Before I go on, did ssomeone mention in the article--and I missed it--that she had given her body, after her death, to medical science? If shedid not do that, OOPS!! I'm causasian and NOT racist and her family deserves compensation. Right is right! She not go into whatever hospital registered as a guinae pig! I agree that medical science needed the tissue, but for goodness sake--go about getting it legally!

    Posted by sandy on February 1,2010 | 12:07 AM

    This is one of the best article I've read, and gives me a lot more perspective looking up the world, want to read the book... I think the family should really receive something, just something...

    Posted by Subaru Obishi on February 1,2010 | 12:08 AM

    Yes! this is a good take on this whole cell mess, scientist playing god and what not, we are so mean to each other, because we think we are doing the right thing(for those in power) for the whole but sometimes we forget to listen to each other and communication is key... I cried reading this article and I'm definitely getting the book, and HeLa's family has a right to be upset.

    Posted by Skybaby420 on February 1,2010 | 12:08 AM

    mysterious yet interesting.. where can i get the book?

    Posted by Jin on February 1,2010 | 12:08 AM

    A great research job.hopefully the family did at some point get compensated.

    Posted by lfrank on February 1,2010 | 12:09 AM

    Great History...I want to know if the family was fairly compensated .....

    Posted by Raj Patel on February 1,2010 | 12:09 AM

    Thank you for a well prepared article. I studied about HeLa cells and Henrietta Lacks in Biology Classes at Jacksonville State University, AL. I was fascinated then and am still fascinated now after reading your article. Good Job!

    Posted by L Murray on February 1,2010 | 12:09 AM

    I can't believe that, in this day and age, they are still selling black people.

    Posted by floob loop on February 1,2010 | 12:09 AM

    I take it that this is not fiction. In that case, it's just a matter of time that scientists will be able to extend the life and health of humans for well over 100 years. Having said that, Helas's relatives need to seek compasation.The pharmaceutical industry owes them billions of dollars.

    Posted by John P on February 1,2010 | 12:09 AM

    Other than this book, has the family received any recognition? I read a newspaper article which stated that the descendents couldn't afford medical care. You'd think that after all this, their care would all be gratuitous. After all, there may be something else in their cells/genes/DNA that might be valuable. Of course, if their is, it has probably already been harvested w/o their knowledge.

    Posted by jujubird on February 1,2010 | 12:09 AM

    I will like to buy this book. e-mail me,so i could buy this book. very interesting.

    Posted by Miguel R on February 1,2010 | 12:09 AM

    I keep seeing - what amount of the proceeds of the book is going to the family? I don't know - did they write the thing?
    I am a writer and if I tell a non-fiction story and I do the research - a person of interest in the story has a decision whether to answer questions or not. They do not automatically have a right to royalties from my efforts.
    If I write a non-fiction book on a mass murderer, should I send him a check in prison? If I write a non-fiction book on an event, do I need to track down everyone that was involved and give them some money?
    In this case, there was discarded tissue and it was used to make some wonderful breakthroughs in medicine. The dumb guy who originally cut the tumor probably did not make a billion dollars - cumulitively there was a great amount of money made with these cells - and a great amount of that was poured back into research to do more good (and make more money, after all we are a capitalist society) But to think that since they did not inform her (HeLa) that it was taken - and at that time there was no way anyone could have told how much money would be involved - she would surely have signed a release has she been asked. What seems wrong was that they didn't ask, but I don't think it had to do with her color - any uneducated southerner - white ofr black would have likely been treated the same. So to make this a race thing or to make this an evil big business thing is wrong. I hate to say it, but if the family wants to make money - write your own book and get it published. Then I would hope all of the righteous indignants here would run out and buy that book. But why do any of that when you can get a hungry ambulance chaser and sue.

    Posted by r scott park on February 1,2010 | 12:09 AM

    it's nice

    Posted by jhayde on February 1,2010 | 12:09 AM

    After reading the article and then the comments, I have a better understanding of what people are most interested in: MONEY AND COMPENSATION.

    It has come to a point in our society that many perceive it is right to seek out compensation for any matter, thus twisting the form of what is real for their own pocket's sake.

    Fact: HeLa cells have saved many people around the globe
    Fact: HeLa cells are scientifically valuable and crucial in finding more methods of helping the human race
    Fact: Henrietta Lack's cells are not the wonderful and precious person Henrietta, they are just cells

    Let's look at the big picture, the many people who have been saved through HeLa cells, and quit focusing on what we can take and claim as a monetary equvalent to Henrietta Lacks.

    Posted by cat on February 1,2010 | 12:10 AM

    There was no compensation because under the law her tissue/cells were considered discard with the hospital or doctors having ownership of the discarded cells--Its case law so the family will never be compensated for their mother's tumor cells- The sons only became interested when they thought they could get compensated for doing nothing. It was the scientist that turn the cells into something of value instead of just throwing the tumor in the garbage--

    I am sure the mother would be happy knowing the cancer that caused her death has saved other lives and has also help cure other health issues for so many people.

    Posted by Michael on February 1,2010 | 12:10 AM

    i remember my father telling me about 1967 (when i was a cub scout)that scientists had cancer cells from a woman and the cells never died even though she had. i am amazed to have my memory jogged by this story 43 years later.

    Posted by bob on February 1,2010 | 12:10 AM

    VERY INTERESTED. BUT IT DIDN'T MATTER WHAT COLOR SHE WAS. HER FAMILY SHOULD HAVE BEEN REWARDED FOR HELPING SCIENTIST INCREASING THEIR KNOWLEDGE. WITHOUT HER CELL, THEY WOULD PROBABLY BE STILL SEARCHING FOR A CURE. BUT, IF IT WAS THEIR CELL IF WOULD HAVE BEEN A PROBLEM.

    Posted by LOIS SIMS on February 1,2010 | 12:11 AM

    Blind people! you still looking at material thing, didn't your preacher tell you that you're immortal?

    Posted by Bwenge on February 1,2010 | 12:11 AM

    creapy enteresting! like to read the book.

    Posted by Jake on February 1,2010 | 12:11 AM

    Great piece nicely done. But as far as the family they should only be compensated for what they themselves donated such as their own cells because they were aware that they were doing it for science and were asked to help with this so they should only be paid for what cells they donated of their own as far as their mother well in those days they really didn't give those choices as to whether you want to donate to science. My uncle was never asked if he wanted to be part of a study group of what radiation does to you during ww1 and he ended up dying from cancer go figure and we never screamed hey u need to compensate!! that stuff was just done back then doesn't mean everything was right but that is they way it was done.

    Posted by Anisha on February 1,2010 | 12:12 AM

    nice book where can i find one of this?

    Posted by dan on February 1,2010 | 12:12 AM

    the story was truthful,intersting and factual. I hope field of medicine understand and relate to it. The amazing contribution of a poor farmer now leads to discovery of very relevant information today. The realization of these medical discoveries came from a simple person whom they got interest with.

    Posted by jay dulnuan on February 1,2010 | 12:12 AM

    Its just research about someone slightly different. What is the big deal???

    Posted by aziz on February 1,2010 | 12:12 AM

    Fantastic TRUE story. How many others like her have contributed to study of genetics etc.? These are our real
    Heroes .... I will buy this book in a NY second good luck
    to the family with getting their "JUST " rewards ....

    Posted by S.C. Tice on February 1,2010 | 12:13 AM

    God's miracle. Please compensate the family

    Posted by sally on February 1,2010 | 12:13 AM

    If any individual is getting paid for their tissue "donations" then every individual (or their estate) who ever donated tissue should get paid. Since Henrietta's tissue has given such unprecedented value, the "HeLa" family should be compensated at a premium, and as soon as possible.

    But I don't think this was racial. I think doctors in the '50s were just generally disrespectful or ignorant of their patients' bodily boundaries and property rights.

    Posted by Mel on February 1,2010 | 12:13 AM

    THIS IS AMAZING,,,A GREAT STORY THAT I EVER READ ABOUT SCIENCES..

    Posted by ASYIQAH QISTINA on February 1,2010 | 12:13 AM

    I'm sorry, but what happened to ms. lack and her family? did she survive much longer? I would'nt think so in those days. The interesting story is of that poor family, not imortality. The world cannot sustain the commercialized or black market extension of the average life span. I can see the curing of cancer and AIDS but this type of biological technology is best left alone beyond that.

    Posted by mike bateman on February 1,2010 | 12:13 AM

    Abolish money, all governments, stock market, banking system, corporations, religion, military, and etc. All of these are enslavement. I am depress.

    Posted by hoai kieng on February 1,2010 | 12:13 AM

    i want this book, where can i find a copy, too much to tell too many to argue, maybe everything good has no end.

    Posted by hildah on February 1,2010 | 12:14 AM

    Thank You for writing this piece. I too had some of the same questions. This is very interesting and I am going to share this story with others.

    Posted by Steph on February 1,2010 | 12:14 AM

    I can't wait to read the book!. I had heard of HeLa cells but didn't realize that they originated from one person. I got chills just reading the article. How exciting it must have been to gather all the material to actually write the book. I am glad Mrs. Lack's family agreed.

    Posted by debcranford on February 1,2010 | 12:14 AM

    Being a student of biology I understand that cells are the foundation for the study of such a science. Regarding on person's comment that we are all just 'animals and the product of evolution', while that may be true, human beings are a different type of animal who make decisions for themselves. As in this day in age consent from the donor must be given before specimens are taken from corpses or live people. Regardless of race consent should have been given before a decision was made on the patient's behalf. The up side of the situation is that the culturization of HeLa cells have led to many great discoveries that has had benefits to the entire planet(human pop). Seeking moneys from a discovery that has shown a benefit to the entire planet is a bit unreasonable and I feel that the Lack family should be very greatful that their mother involuntary donation has saved the lives of countless people around the globe including their own.

    Posted by Harv on February 1,2010 | 12:15 AM

    So if her cells were immortal, then how did cancer kill the cells that caused her death?

    Posted by LaLa on February 1,2010 | 12:16 AM

    :D GREAT THE FAMILY IS SMART THEY SHALL GET EVERY DIME YOU WHITE PEOPLE STOLE FROM THEM AND THEY MOTHER GOD BLESS THAT FAMILY.TRYING TO GET FAME AND MONEY FROM HER DOUGTHER BY STALKING AND TRAPPING HER SMH YOU ARE A SICK PERSON!!!!!!

    Deborah’s brothers, though, didn’t think much about the :cells until they found out there was money involved. HeLa cells were the first human biological materials ever bought and sold, which helped launch a multi-billion-dollar industry. When Deborah’s brothers found out that people were selling vials of their mother’s cells, and that the family didn’t get any of the resulting money, they got very angry. Henrietta’s family has lived in poverty most of their lives, and many of them can’t afford health insurance. One of her sons was homeless and living on the streets of Baltimore. So the family launched a campaign to get some of what they felt they were owed financially. It consumed their lives in that way.

    Posted by jesus lady o88p88 on February 1,2010 | 12:16 AM

    If the scientists did not use Henerrita cells for generate income by selling them to other researchers, then, there wouldn't request for proper compasation. But, since the scientist sold Ms Henerita's cells, her family deserves a share of the income generated from the sale of those cell lines, my advise is to them is to hire a business legal counselor to help them properly recover what would have been their share

    Posted by David Wasanyi on February 1,2010 | 12:16 AM

    me and my husband read this story together and thought it was very interesting and like so many others would like to know if the family ever received any monatary gain from this it seems to me if they are poor and can not even afford to see a doctor when they are sick that someone with some power would do something to help this family.

    Posted by bonnieandfreddy on February 1,2010 | 12:16 AM

    So...are some of the book's proceeds going to Henrietta's family?

    Posted by alissa on February 1,2010 | 12:16 AM

    Sadly most peoples comments highlight the notion that "People are for sale". Why would they compensate a family thats mother/wife's blood was sold to spread the HIV virus to so many innocent people disguised as vaccines and medicines? Why would someone WANT to take money that has done so much wrong and should be a crime agaisnt humanity! WAKE UP PEOPLE! This is a classic scientific research gone wrong and taken over by big business gurus trying to make a few bucks over the years. Scientists are not the probelm here, don't get me wrong. This is just what happens when bad people take advantage of our life saving systems like science and use it to depopulate the earth. Ok.. ok.. I have room for positive perspective. This article was written well. =) But don't be fooled, it lacks some important real facts of the matter.

    Posted by TeaCaptain on February 1,2010 | 12:16 AM

    This is a very amazing story, and if this was done without any family member consent and knowledge, they should be compensate for all those years.But it will never happen.

    Posted by JR Rosell on February 1,2010 | 12:16 AM

    Fascinating.............

    Posted by Rhey on February 1,2010 | 12:17 AM

    It makes me wonder if there were any other cells taken from other people, and just how many times were cells taken from other people? And since when and how long? Curious.

    Posted by Maggie on February 1,2010 | 12:17 AM

    Sigh--it seems like America will never a color-blind society, as witnessed by the nationalistic expressions of some authors' comments, authors who turn a science story into a black nationalism forum. To set the record straight, all Henrietta did was get cancer and have her cells collected by scientists. How does this count as an achievement to black history? What were the races of the scientists who actually developed the vaccines and made other discoveries resulting from the cells? What is more important, the idle lump of coal or the person who discovers a use for the coal? Of course they are both important, but the derivation of benefits of an otherwise useless object deserves more applause than the otherwise useless object itself. My point is not to put down Henrietta or black people, but rather protest the racializing of everything in our society. For those whose comments didn't mention anything about race (which were the majority)--I applaud you as a beacon of progress. To the few who did the opposite, I write my comment.

    Posted by Chris belanger on February 1,2010 | 12:17 AM

    I am sure that any lawsuit initiated by the family would not only be a loss on the families side but just a waiste of much needed money. I am sure that because the cells have been purchased (and probably copywrighted) the law will side with science. But I am also sure that Scientific researchers will provide outstanding medical coverage for the descendants of Henrietta if those descendants allow them to take small tissue samples for further testing. I saw that one person asked if the family could initiate a lawsuit against the original scientist and the answer would be no. Because the scientist is most likely dead. And in our society the sins of the father do not transfer to the son. It would also be hard to make a case against the eploing company of that scientist because the leaders of that company (who made the decisions at that time) would also be dead. It would be the same as initiating a criminal case of mass murder in the first degree against the Vatican and Mecca for their involvement in the crusades for Jerusalem. Leaders change and once they have chaged leadership cannot be held responsible for the crimes of past leaders. Just to give a little legal insight. But it is possible that a court would side with the family on ownership of the cells because the family would own the body after death, and those cells were part of her body.

    Posted by delta_steve on February 1,2010 | 12:17 AM

    Great job, Henrietta Lacks should be IMORTALIZED

    Posted by Etim ESu on February 1,2010 | 12:18 AM

    Not everything in life results in a win win situation. Just knowing that a piece of her has helped so many is payment in full...

    Posted by Wes on February 1,2010 | 12:18 AM

    This story is really great and amazing...though she's died already but her cell lives as long as human race exist.

    Posted by Dzaehnie on February 1,2010 | 12:18 AM

    How exactly are her cells immortal, i'd love to know how thats possible and find out all the details, is it in the book?

    Posted by seren on February 1,2010 | 12:18 AM

    Tuskegee experiment all over again the man infecting our people once again !!!

    Posted by slim on February 1,2010 | 12:18 AM

    Now they just take the cells from unborn babies instead.

    I suppose their families don't mind that their unborn children and grandchildren are being killed to be used this way - as long as it helps someone, right?

    God bless America; we really need it.

    Posted by Meg M on February 1,2010 | 12:18 AM

    This was an interesting article. Research for cures and finding the right way to handle any serious illness is important. Unfortunately, many poor, especially blacks who used as ginney pigs by laboratories. During these early years in search for a cures. There were horror stories that were hidden from the public about the things done to blacks that lived in the area of Johns Hopkins hospital in Baltimore. People were reported missing. Nothing ususally was done, because the families were poor and lacked the financial needs to obtain any type of search or the backing for support for a search. These are some examples. A woman was not given any anesthia while undergoing surgery. She went into shock. A man was getting a tooth pulled and given no pain medicine or anesthia. A lot of times the disease was not treated and the patients suffered because the medical team was seeing how long a patient could survive w/o treatment. I used to wonder why older black people did not like going to the doctors, esp.the hospital, and that was because they either witnessed or knew someone who suffered becauese of some of the horrible situations that most black and poor persons had gone through during those early to mid 20th century years. Thank God it is not as much. Most third world countries face these types of conditions now.

    Posted by Karen on February 1,2010 | 12:19 AM

    It's sad that quite a few people commenting here have the same level of understanding as Henrietta's husband.

    Posted by caftor on February 1,2010 | 12:19 AM

    An article about how it was discovered that HeLa cancer cells had traveled airborne and invaded other cancer cell cultures was printed many years ago.

    Posted by John Ferguson on February 1,2010 | 12:19 AM

    To surreptitously obtain any part of this woman's body and use it for gain in any respect no matter how noble is diobolical. Then, to add insult to injury,the family shares no part in the financial prosperity others have so gldadly enjoyed for years. It is a sad day when every man can do that which is right in his own eyes.

    Posted by Mike S on February 1,2010 | 12:20 AM

    What say we revisit the Betty and Barney Hill event. Their DNA's should be of extreme interest.

    Posted by J. Rain on February 1,2010 | 12:21 AM

    Wow!!!!!This is something else!

    Posted by Sydney on February 1,2010 | 12:21 AM

    People are divided on the issue of monutary payment to the family. According to the article,Henrietta's cells were taken without her permission. No matter how you look at it this simple act was morally wrong. The issue of money is mute. The scientist whom took the cells benefited, the pharmacutical companies have benefited from it. Is it wrong for the husband who lost his wife, the children who lost their mother or the daugther Deborah who never got to know her mother to be denied to benefit from it. They have the right to know that part of their loved one involuntarily saved millions of lives from a polio epidemic,advanced gene mapping and vitro fertilization. I lost my mother three years ago. I had the benefit of getting to know her, what made her smile. The sons I feel should be angry. Her family should be paid for the mental anguish suffered at the hands of early 1950's toleration of exploiting a persons medical condition for profit. The sons learned about there mother only after finding out there late mother's cells were being sold and that the scientist were looking to get new samples from them to see if they have the same gene. When my mother died it broke my heart. If, I found out that my mother's cells were illegally taken and being used I would be looking to sue someone for violating my mother's person. Henrietta was a human being first. Just because she was African American does not give society the right to take advantage. I would only by the book if I new that profits from the book were going to establish a fund for the Lack family. Maybe even a scholarship established in her name. Being an African American female, I find it fasinating that people want to dismiss the family receiving monuetary payments because they feel here is another Black person wanting restitution for wrong done against them. This was someones mother, not a test subject. Morally wrong is just wrong. I would argue the same way if is was someone of another culture or nationality.

    Posted by Sylvia on February 1,2010 | 12:21 AM

    Great story, I think this story should be told everywhere. I also hope the family was compensated. Thanks for sharing!

    Posted by Heather on February 1,2010 | 12:22 AM

    As sad as the fact she could not be saved from metastatic cervical cancer fifty years ago, this cancer is still uniformly lethal if not resectable.

    Her Hopkins doctor hopefully took the best care of her with the available technology, and hopefully showed empathy and compassion, if only to keep her comfortable. If so, the family owes him gratitude, since he is likely dead, why/how should he pay them any compensation.

    I pray that the young ladies in Baltimore read this book and avail themselves to something Ms. Lacks did not have: PAP smears, HPV vaccines, and HPV testing. These screening interventions can nearly prevent death from cervical cancer.

    Hopefully they will appreciate 50 years of progress that science has provided to help them.

    In Baltimore, many mothers of teenaged girls refuse for them to be vaccinated due to ignorance.

    Posted by KG on February 1,2010 | 12:22 AM

    Wow! what a story. I am not one to be very intrested in science unless it has to do with hi tech gadgets and stuff but this story blew me away. I clicked on it by accident but i could not stop reading once i started. Great job author, i am looking foward to reading the book.

    Posted by malang Jay Saidy on February 1,2010 | 12:22 AM

    A movie about it would be nice for her recognition!

    Posted by Pala papapa I m lovin it ! on February 1,2010 | 12:22 AM

    Sounds like a good read.How many cures made by this find?

    Posted by Stephen on February 1,2010 | 12:22 AM

    Oh thats our lesson in my immunology and serology class.... wow so amazing it was published.... i really didn't know that hela stands for henrietta lacks ... i thought that was just a name given by the scientist taken from whatever they think could be a good name for the cells .... sounds refreshing in my head for some lessons i forgot .... thanks for the info .... its so nice reading it ...since i have some background about this topic ....
    And the family should be compensated because the cells of their mother made a difference in the field of science ....it gives contributions, it made wonders,cure some disease and made vaccine out of her cells .... thanks to her cells, it benefits alot of people ....

    Posted by jen on February 1,2010 | 12:23 AM

    Honestly i thinkthe family should be compensated being that the tissue was taken without permission.Additionally,the scientist had no right making money off the cells without the families permission.

    Posted by Silver on February 1,2010 | 12:23 AM

    Some 46 years ago I lost a child to what was a deadly disease. There was a crucial question that they had not been able to find the answer. I signed for them to do an autopsy. Six months there was a small article in the newspaper that said they had the answer and were working on a solution with the information. That disease is almost always curable now. I am very pleased that my child may have been the one with the answer. That something good should come from such sorrow is a consolation. We are all on this earth for a reason. The drs owe me nothing. That children are living today that would not have survived this illness is the greatest gift in the world. Bugg

    Posted by Iris Stone on February 1,2010 | 12:24 AM

    What a wonderful thing that mankind's understanding and the capability of medicine could be advanced to such a degree by the remarkable cells of the culture taken from Henrietta Lacks. What a pity that some would want to turn this wonder into a racial and compensation issue. And what a waste of a journalist's life to "become obsessed" with exploiting the woman and stirring up her descendants into this controversy. Henrietta Lacks and her family were fully compensated by the fact that she received a doctor's best care and efforts to save her life. She didn't walk into a clinic and offer to donate something. She came in seeking medical help, and she got it. Now to her descendants: take responsibility for your life and work your own way through. No one owes you a living.

    Posted by foghorn on February 1,2010 | 12:24 AM

    I am literally a scientific moron.....but I can't stop thinking that maybe her cells have survived for so long because of the cancer, because of how ruthless cancer is, how strong it is! Maybe this story is yet another reason why the ultimate cure for cancer must be found!! None the less an amazing story......here's to hoping the book will shed some light for me and proof me wrong!!

    Posted by Cherie on February 1,2010 | 12:24 AM

    Just remember folks, everytime someone goes to a doctor's office or into the hospital, all kinds of forms are shoved in your face to sign. NOW you know why. (and they won't treat you unless you do sign those forms, remember that too)

    You also rarely have the time to read these forms in order to find out exactly what they really want. So, when the medical profession tries to place the responsiblilty on the patient about their own care, just remember exactly HOW much you are being charged for the office visit, surgical fee, hospital stay, medication, xrays, tests, etc. A lot of people have been bankrupted by the medical profession, while they take advantage of you. Now, they want to put your personal information online. You sign over your rights to them.

    Posted by Georganne on February 1,2010 | 12:24 AM

    Makes me think; Consider, if HeLa cells, piggybacking on dust particles, being used for numerous medical and scientific purposes, with the ability to "infect" cell cultures... are our own healthy cells safe? What if through all of our advances in medicine, we've only been provoking the pitbull? What if it's only carelessness that's been causing the steady increase in cancer rates? What if the ghost of Henrietta Lacks is slowly killing the world? What if the apocolypse is already upon us?!

    *sees dust particle in the air and runs out of the house screaming*

    I have to say, I'm not sure about the family being compensated. Do they deserve money for being related to Henrietta?

    Posted by Eugenia on February 1,2010 | 12:24 AM

    It's funny to me that so many people (black, white, latino, etc.) are asking if this woman's family ever got any money...lol...i love you america!!!!

    Posted by Dee Pee on February 1,2010 | 12:25 AM

    It is very interesting story, but what the law says about the right of a person whose cells have been taken for scientific research? I think it is high time now the law should be enacted to protect not only the Henrietta family but also all other people who will be involved in such incidences.

    Posted by Helen Benjamin on February 1,2010 | 12:26 AM

    I'm curious as to what prompted the scientist at Hopkins to use Henrieta's cell in specific. Why hers?

    Posted by Berti on February 1,2010 | 12:26 AM

    WOW

    Posted by Henry on February 1,2010 | 12:26 AM

    Very interesting story. Where is the book???

    Posted by Karani on February 1,2010 | 12:26 AM

    so she should be given credit.. not just the doctors.

    Posted by ryche on February 1,2010 | 12:26 AM

    I enjoyed the article and will purchase the book for further information. I wanted to make a comment about the 100s of posts I have seen. Thanks be to God that her cells were taken. Many of us would have died in infancy without her. I understand some peoples bitterness toward the "white man" that took the cells and in turn helped to make all of those life saving discoveries. Truth be told, Black History Month is a wonderful opportunity for students to learn, unfortunately what is taught, Slavery, is not the whole story. Which in turn makes others angry that the black man has been kept down. I have seen how the black man or woman can be very successful by working. There are those that feel they are "owed" by the white people for the rest of the black persons existence. Give it up and remember we all have the same insides and need to be thankful for the discoveries that this beautiful woman has helped to make. She deserves a larger place in history, not tons of compensation to every black person in existence. Beautiful story, beautiful woman, I wish her family in future generations only the very best. She is looking down on humanity and smiling for sure.

    Posted by Kim on February 1,2010 | 12:27 AM

    @Colleen

    Some people may think that the cells aren't immortal. True they are not literally immortal but they are biologically immortal. The difference is is that they can die if they are purposely killed. Either by chemicals or lack of sustinence. Normal cells will die after so many reproductions. They are limited by many factors. One being that every time they reproduce, the telomeres get shorter, and eventually are gone. Then the cell stops dividing. It's called apoptosis. But it is common with cancer cells to never stop dividing. If noncancerous cells were to reproduce like this then a human could potentially live forever, save they weren't murdered or in a car accident or the like. A good example to look at are the giant sequoia trees. If it wasn't for the fact that they fall over from getting so big or forrest fires, scientist believe they would never die. There is no sign of aging.

    Posted by Brad on February 1,2010 | 12:27 AM

    What is the exact name of the book and author?

    Posted by Shannon on February 1,2010 | 12:27 AM

    I would rather say this is something relates to KARMA, though the blacks do not really believe in Buddhism

    Posted by John on February 1,2010 | 12:28 AM

    but the real question is, when scientists find out HOW this cell is immortal, will that lead to living human bodies to be immortal?

    Posted by dan on February 1,2010 | 12:28 AM

    Why is everyone so worried about if they ever got the compensation? When you have blood taken do you ask for compensation for anything that might be discovered other than the reason the blood was taken? When you get your hair cut, do you ask for compensation just in case it makes its way to a wig maker? How about this, do you ask for compensation for the trash you throw away? That gets turned into methane gas later sold to power homes, parks, golf courses. Also, say that they knew right away and wanted compensation, however were unable to get any. So because compensation could not be given, they did not allow it. Then were would we be today? As soon as I started to read this I was waiting for the part when the family would want money. Everyone is always worried about money and never about the greater good or the advancement of the human race and peace on earth.

    Posted by Kevin on February 1,2010 | 12:28 AM

    I was very intereste in reading this article and surprise it took to now for someone to let us know that a woman of color has contribute to the science world...great peace i would love to read more..

    Posted by monique on February 1,2010 | 12:29 AM

    Nothing 'subtle' or 'complicated'...a doctor used a patient's body without her consent. The Nuremburg trials denounced experimentation on people without their informed consent. But we have learned nothing from the old saying that the ends does not justify the means. Shame on the author for presenting the woman's life as oh well, we'll all benefit from the affront on her personhood and dignity.

    Posted by Deborah on February 1,2010 | 12:29 AM

    Having a blood platelet dysfunction makes me LOVE this story. Thanks to this woman and the Scientist there is a chance that stem cells could cure me and my family and millions of others of so many things. I say Thank You to Her

    Posted by Cynthia on February 1,2010 | 12:29 AM

    I never read anything in my computer. I mean not like this. For some reason, when i see the pic. I start reading it. Yes... I would love to have the book myself. Where can i find it?

    Posted by Rose on February 1,2010 | 12:29 AM

    This also happen with our family. We were involved in research and did not get compensated.

    Posted by ow al on February 1,2010 | 12:30 AM

    Very well written, and a great view of what is sometimes forgotten about science. I have hope that the family received even just a 1/100th of a percent of the money made would make them rich beyond their dreams. And I hope that Deborah got some of her information about her mother; I know the scientist can't but if the family is discussing her, hopefully she got to learn some about her Mom.

    Posted by Ben on February 1,2010 | 12:30 AM

    As usual the poverty of the poor does not count! Including the writer of this book, owes Henrietta Lacks' and her decedents. Maybe with that money one of her decedents may be the doctor to cure cancer. Not to sound racist but I get the impression only certain people can contribute and the rest are worthless! Sounds like a Frankenstein movie using the victim as an excuse to benefit over and over again. Can't kill nothing and nothing won't die. But the poor is always used and not permitted to profit or win at any cost! Reward the family, pay them royalties, and be done with it. If a certain plant producers can raise hell about their genetically alter pollen getting in to the next door neighbor plants by accident, and want to charge them, then why can't these nice folks take advantage of the unknown ways of science. All well, capitalism for the poor and socialism for the rich, as they share the booty. PS Doctor and Weathermen are a few of the only professions that can be wrong and still get payed! I still respect both profession only if human sensibilities are respected.

    Posted by Supertech20020 on February 1,2010 | 12:31 AM

    the scientists owe the family. they must help the family considering that the family lives in poverty. moreover, the book must be nice.

    Posted by lawrence on February 1,2010 | 12:31 AM

    Not to be cynical, but I guess that Rebecca Skloot will not profit from the book at all ? How endearing of her to champion the cause of this less than well known African American woman who has successfully contributed to vital research and discoveries for all humans. Imagine that! No don’t think I would want to read the book. The article says it all. Also, we are not all “dumb” as some suppose. And yes, even when politicians and others “talk down to us” , the majority of the American public regardless of heritage know when we are being demeaned. No matter how eloquently put or defended . Lastly, an injustice is just that, not just.

    Posted by Woodsey on February 1,2010 | 12:32 AM

    What an amazing story! I can't wait to read the book. It's really interesting how her cells can remain alive after she has passed on. Someone should really make it a movie.

    Posted by Betty Shepherd on February 1,2010 | 12:32 AM

    As a Republican I have to say I give credit to Obama for a new era of "near" multi-racial unity and that's about it. But while most of us see this, we forget the disgusting era of racism that we inherited. This is an infringement of the most basic private property rights... your own body. Not just that but the fact that no royalities have been given to any of the family members. It's so ironic and sad how her cells have saved thousands of lives and yet most of her family lack health insurance. I am truly disgusted how surreptitious money mongering executives and racist scientists knew the world wouldn't care about "colored" woman. I'm sure this woman didn't know her cells would be used for revenues of multi-national pharmaceutical companies and profits for their CEOs because if she did I'm sure she would have wanted her family to at least get a small percentage of what they the scientists and companies legitimately do not have full rights to.

    Posted by Lance on February 1,2010 | 12:33 AM

    she doesn't look poor in that photo!!! is that a fur that she has draped around her? I'm glad that the story is being told because no one really thinks of black people when it comes to any kind of notoriaty at all.

    thanks for telling the story

    Posted by duck on February 1,2010 | 12:33 AM

    I also want to buy the book. I am in the Philippines. I hope it gets here soon. It should be fun reading.

    Posted by Robert R. Navera on February 1,2010 | 12:33 AM

    Face it, Henrietta was probably just happy to be rid of the tumorous cells, and wouldn't have cared less if they were used. Anyone who has something like that is likely willing to contribute those unwanted cells to help keep their children or grandchildren from getting the same disease. It's sad that part of her family was homeless, and it would have been nice if the profiting research companies were to help. However, if you gave away brush and branches that you wanted out of your yard would you really expect to be compensated if someone carved it into a masterpiece? Another question I have is this: If a white person had the polio vaccine, does that mean that they are now just a little bit black? Just some food for thought in our foolishly color conscious country...

    Posted by mic on February 1,2010 | 12:33 AM

    instead of saying black woman from virginia the writer could have said an African American woman from virginia!

    Posted by andrian on February 1,2010 | 12:33 AM

    great achievement for human race..the family shuod be given share for the billios of income..in reality greediness is a component of a success,...but at the end,..only god can decide for all of us..

    Posted by ryan on February 1,2010 | 12:34 AM

    So worried about suing and money, her cells have saved billions of our lives and still does every day! Who cares if she was black, stupid to even mention it.

    Posted by Lils on February 1,2010 | 12:34 AM

    Nice piece.It got me glued to my seat.A very revealing story.God bless her.

    Posted by Davis on February 1,2010 | 12:35 AM

    I would like to know how a lady with these kind of cells died...

    Posted by veronica on February 1,2010 | 12:35 AM

    Good story after atlantis!

    Posted by lubis grafura on February 1,2010 | 12:35 AM

    Very nice piece. And yes it was devious and malicious to use her cells without letting her know or informing her family,,, only to come back to them when they were desperate and wanted to clear out "contamination!"

    Posted by Joanne on February 1,2010 | 12:37 AM

    I understand you want to sell your book! But, I wish you would have answered all the questions instead of leaving us hanging! I'll NEVER read a little book much less a big book. It's a great story & enjoyed it.

    Posted by Suzie on February 1,2010 | 12:37 AM

    I really don't understand the "racist" tone and attititude. I am a black woman and am American. I didn't grow up in Africa even though my ancestry dates back there. I am successful because I have worked hard to be successful. I think this is awesome research that has been done but I don't know why "we", blacks, have to resort to being so proud and yet so angry over something like this. Sure, maybe there should be some restitution, but please stop looking for a hand out. You make all of us look bad. At the end of the day, I am proud of what I have accomplished on my own merit and not what someone "owes me" or gives me; I earn it. Thank you Henrietta Lacks for your contribution to "mankind" (and woman) of all color, race and creed. You are certainly a hero to many who couldn't afford to pay you what your worth for the invaulable, life saving treatments you have given them.

    Posted by Kayla on February 1,2010 | 12:37 AM

    I hate how her children (excepting the daughter) didn't care about the enormous benefits their mother's cells had contributed, until they found out they could got rich off it. Such a disgusting, hard, self-centered culture we live in. Personally, I'm grateful to Henrietta for what she did (albeit unknowingly). God bless her.

    Posted by Jackie on February 1,2010 | 12:37 AM

    its great book... i can't wait to reaad that book.

    Posted by Bernard DJ on February 1,2010 | 12:38 AM

    I am tired of black people being treated with no respect. Everything is not always about money. This women should of had the right to say that it is alright to take her cells, dying or not. alright it's great that the cells opened a Science door. Henrietta should be in the history books, and be given credit for what she contributed.

    Posted by Deborah A. Hubbard on February 1,2010 | 12:38 AM

    I really enjoyed reading this article. I am amazed at what those doctors and scientist were able to do with the cells of Henrietta Lacks. It really made me appreciate the Creator even more. The fact that those cells survived so long just reinforced in me that we were made to live forever!

    Posted by Margie on February 1,2010 | 12:38 AM

    1. Doctor's took something without consent.
    2. Is her family being compensated/receiving royalties for this?? I do hope so, for this discovery has changed the condition of Man and has spared the loss of millions.

    Posted by Frances E. Mulero, Killeen, TX on February 1,2010 | 12:38 AM

    Offhand, this sounds like a load of nonsense, i.e. a long story about nothing. The cells must have been subcultured (a normal thing). It can't be the original cells that are still alive.

    Posted by Miles on February 1,2010 | 12:38 AM

    It is still hard to believe that those who make money off of others still don't want to share the profits for as long as they possibly can, if ever! To the family: Don't let the past consume you, rather let it push you foward into the future of understanding and the forgiveness through Jesus Christ. My prayers are with you all! P.S. Great story, obviously this took you some time to collaborate all this information.

    Posted by Burnise Perry Jr. on February 1,2010 | 12:39 AM

    This is a book worth reading, l think l will put alot of effort in finding the book. Great story!!!

    Posted by Valentine T Chibwe on February 1,2010 | 12:39 AM

    What's sad is that this is not a part of our American history that's taught in schools. She was a black women that continue to make a huge contribution to medical history. Many seem to be concerned if her family was compensated? I feel the bigger question is "when will this be put into our history books?" It's sad that history about Aferican American's contributions to our society and our America is only shared during the moonth of Feb

    Posted by Gwen Guy on February 1,2010 | 12:40 AM

    The scientists research is the begining.Waiting the final fruitful output for human being.I disagree personalizing the issue with the sampled woman.I appriciate the 1st (Dr) person who purposly took sample to reache this current amazing result.

    Andinet Zeleke
    Addis Ababa
    Ethiopia

    Posted by Andinet Zeleke on February 1,2010 | 12:40 AM

    This is an amazing article,I guess the book wuold be really interesting, most people would think of this as a sci-fi (science-fiction) story.

    Posted by dorothy nguyen on February 1,2010 | 12:40 AM

    it is so amazing i just read another book where i found out about this story, i was wondering where i can learn more, and here it is. i am running to buy the book.

    Posted by iwonayoga on February 1,2010 | 12:40 AM

    Unfortunately, all too often people become heroes after they die. Sometimes they remain silent heroes. Luckily, her family was made aware while they were still alive. Maybe, they can be at peace with that eventually. By the way, I enjoyed the article; It was refreshing.

    Posted by Adrienne Davis on February 1,2010 | 12:41 AM

    Awesome story.....I too have heard of HeLa cells but did not realize the possiblities....I too believe the family should be compensated, especially if the lab that provides the HeLa cells to others is making a profit.

    Posted by LeAnn on February 1,2010 | 12:41 AM

    yep its great story.....wish thy culd 've told the woman she deservd to knw...thank u!!!

    Posted by Phatsimo on February 1,2010 | 12:41 AM

    This woman as miraculous as she may be... still needs to be protected and respected not as a scientific experiment... more as the human being that GOD created. Her family has rights in her behalf. Monintary? So be it. She needs to have her say... and that would be through her family!! They need to be compensated for all the good their MOM did without permission. Everyone knows that you (scientists) proceeded with your own needs and did not consider hers. I appreciate all that was learned for mankind.... Now compensate HER (her family)for what you used and learned.

    Fair Is Fair.....
    Be Honest and Do the RIGHT THING....
    The Family needs to be Compensated!!!!

    Always True diannagacik@bex.net
    DiAnna

    Posted by DiAnna on February 1,2010 | 12:42 AM

    What is wrong with you people. Is the only thing u can think about is to sue. Get a life. This woman was wronged and thats too bad but in my mind she is a hero

    Posted by wane on February 1,2010 | 12:42 AM

    I hope everyone gets what they deserve. In the realm of humanity this will benefit all of us for generations to come. I hope everyone can see this, and not make it anything more than the miracle it is. Thanks for turning me on to this RQ. Love ya, rich

    Posted by rich jonson on February 1,2010 | 12:42 AM

    Considering what was written, more than likely biologists today have already cloned these cells. Also, this is all that we will ever know. If something to this extent was released, this would cause drug affiliated companies who survive off of many defects or ill people to close as a result of people being cured. Today, one can believe that there are many cures. However, kept away in secrecy. If a drug that can cure people be released, this economy would suffer even further than it has. Therefore, this amazing story and discovery will die in vein along with Henrietta Lacks.

    Posted by Andrew on February 1,2010 | 12:42 AM

    Wow! That book gave me a curiosity feeling of some sort. I'm buying that book.

    Posted by christian loyd on February 1,2010 | 12:42 AM

    I wonder where her ancestors came from. Do her offspring share this trait? There is so much to be learned here. This is so important today with all our medical and scientific advances. What could a new sample unlock? Seems to me that this woman deserves a greater place in history. I hope she gets it.

    Posted by Michael on February 1,2010 | 12:43 AM

    " Everything is all possible to GOD ALMIGHTY WHO MADE HEAVEN AND EARTH. THEREFORE, THIS IS GOD'S WAY. Thank you Lord for this master peace of yours as an instrument, (HeLa's body) Im pretty sure she's in Heaven now. Who knows, that cells might save my brother before, that he almost get a folio problems. I really don't know, but, I beleive in God's Miracles. Thank you for sharing this...if i see the book, definitely i would buy the book, hope i can afford. God Bless You Henrietta!

    Posted by ave on February 1,2010 | 12:43 AM

    Very interesting, I enjoyed you being involved in this. The family needed to know about their loved one. This is amazing story, I just love this kind of stuff. I would like to read the book. Well hope Henerita family gets some kind of resolvement and her daughter can learn more about her mother. Thank you for your efforts and sharing this with everyone, that's wonderful. But I do believe she should have known about what they did at the time. That would have been only right, no matter what race or sex you are everything the doctors do should be explained exactly how and what has been done to you. God Bless her family!

    Posted by Michelle McLean on February 1,2010 | 12:43 AM

    interesting...

    Posted by zarah on February 1,2010 | 12:43 AM

    Knowing what is known now about the link between cervical cancer and the human papailloma virus.......did this virus cause her cervical cancer?

    Posted by cherie on February 1,2010 | 12:43 AM

    On the issue of compensation, in today's world, asking a patient for a sample of cells for 'research purposes' involves a full disclosure statement informing the patient that these cells of the tumor they are donating will be immortalized and sold for research purposes. There is no compensation.

    This policy developed over time due to situations like these. The scientist who did this was not malicious in his actions - he was driven by seeing a new type of tumor (perhaps one that was aggressive in growth) that could lead to a stable cell culture line for research .. not monetary greed. The money made from the sale of cell lines isn't great. There is a lot of money used to feed the growth, storage, and testing of the lines to ensure they are clean and non-contaminated with growth from other cell lines, which is extremely important when you do research.

    Posted by Kristen on February 1,2010 | 12:44 AM

    Awesome. This has opened my mind more and I wonder how many more in vitro fertilizations were administered without family permission...??? Science and doctors are to blame or praise whichever the situatin outcome. But remember something created the cell first. Thank you very much. Life goes on. Praise God.

    Posted by Donna Skalnik on February 1,2010 | 12:44 AM

    This was a very interesting read...I liked it and it taught me something I never knew. Heck, if my cells will help save lives or invent medicines to help people than I'll vonteer some cells. At least maybe someone will remember me for something I did positive and good in life. And back then it could've been whire scientist using a black lady to expeiriment but maybe she got the last laugh by becoming such a huge diffence to all mankind. :)
    PS....Now I have heard and know what Hela cells are and where they came from. Thanks for the lesson:)
    Anthony

    Posted by Anthony on February 1,2010 | 12:44 AM

    Where did anyone get the idea this book is about race? If that's what you get out of this, you need to work on your reading comprehension skills. Until we absolutely refuse to notice (or at least mention) a person's race, sex, age, whatever, we are ALL doing our part to keep discrimination alive and well in the good old U S of A.

    Posted by Trinity on February 1,2010 | 12:45 AM

    Well, when the descendants of the tribe that sold Manhattan Island for a handful of beads get compensated...yeah, then we can deal with this issue with no problems. Seriously, if you're going to force "race" into this literally awesome story, why not go all the way back?

    Posted by Dawn on February 1,2010 | 12:45 AM

    This story is very educative to us the young people, it gives us a pratical understanding of science and what comflicts those vested with the responsibility of carrying out researches can cause if they are no guiding policies in the way they operate on human science. i would be glad to purchase the book in which books store in southern African countries like Zambia can the book be found. And to the writer, i say congrates for the passion that you never lost from the age of 16 years u where still focused on the goal u wanted to achieve personally you are an inspiration to me God bless you.

    Posted by Faith Simukoko on February 1,2010 | 12:45 AM

    weird stuff.. but temptation is there to find and buy this book..

    Posted by jesa on February 1,2010 | 12:46 AM

    simply amazing....

    Posted by me on February 1,2010 | 12:46 AM

    This is absolutely ridiculous. The doctor took her cells without her knowing! Major injustice. Black people probably have immortal cells different from other races. The family has received nothing for this injustice. Shame on anyone involved in this and made money off of it!

    Posted by Evergreen on February 1,2010 | 12:46 AM

    thank you for the interesting article. I hope the family will receive some money for the contribution H.L has made to science and mankind!

    Posted by milonga on February 1,2010 | 12:46 AM

    Facinating story. The implication is that the individual has legal rights to their own cells and any benefits derived from those cells.

    Those interested in the legal and ethical aspects of this concept should take a look into the Human Genome Project and the subject of Patenting DNA Sequences.

    The question at the heart of this controversy is "should a group be able to patent a DNA squence?" (the NIH began applying for patents in 1991). All medical benefits, commercialization of biomedical research, and genetic therapies derived from these sequences could then be held by limited groups of people. Basically you could have a cure for a genetic disorder with only a single company having the legal right to produce the cure.

    Posted by Rkeith on February 1,2010 | 12:46 AM

    I hardly think a cancer diseased ovary would need permission from its previous owner, so that science can progress on said cells from diseased ovary.

    I would be delighted if my Mom or Sister or Relative had living cells to celebrate Medical research, etc.

    I would not want, nor would I expect payment. Medical Research is VERY expensive and I would want to know any funds were spent on RESEARCH. WHAT A LIVING TRIBUTE TO THIS WONDERFUL LADY AND HER LIFE.

    Posted by Meghan on February 1,2010 | 12:46 AM

    This is a very interesting story... however the family NEEDS to be compensated!
    While this occurred several years ago, without Henrietta's knowledge...that would be a multi-million dollar lawsuit these days. The HeLA cells have done amazing things for the progression of science. But "science" is a MAJOR money maker. Yes good for humanity... but let us not be naive... several white men profited from this women's cells....for decades!

    We know that race is in fact not biological, but socially constructed.

    Posted by spinsterlarue on February 1,2010 | 12:47 AM

    Great revelation, I hope that this book will get to African Schools. Please let me know how to get this book or ccan I download it via the internet? The family should be rewarded. Once again, Great Reveelation.

    Posted by Uchenna on February 1,2010 | 12:47 AM

    Very interesting article. My Genomics teacher told my class about it today. To the one poster, it's true that everything that lives dies, but these are CANCER cells. Cancer is uncontrolled proliferation of cells due to certain mutations. As long as they have a source of nutrients, they will theoretically divide FOREVER. I'm not saying that the family should make money for everytime her cells were/are used, but they deserve something since the sample was taken without consent. These will probably be the cells used when a cure for cancer is finally found. I love science! :)

    Posted by Alexa on February 1,2010 | 12:47 AM

    Amazing story! Has my curiosity peaked, and I will be getting the book, even though I am not one to read often. This will be my first book purchased that is not school required.

    Posted by Krazyivan on February 1,2010 | 12:47 AM

    Isn't this just one of countless examples of how bigtimers steal from little people and kept it secret so that they can keep on doing it over and over again?

    It took more than 10 years for millions of ordinary people in the world to find out the hard way how Wall Street bigtimers took people's life savings for a song by cooking up all kinds of legitimate ponzi scheme wrapped up in fancy names such as "trust funds" and et al. The Biotech bigtimers are even more savy with the secrets of Hela cells because it took more than 50 years for anyone including surviving members of the unsuspecting donor to find out the truth.

    Welcome to the hard reality of business as usual.

    Posted by Ben Hu on February 1,2010 | 12:48 AM

    Amazing story. SOMEBODY has made money from this woman's cells. And somebody, including this journalist, will CONTINUE to make money. I hope the family gets all they can get. It's not 'just cells'. That's part of a human being.

    Posted by ohsnap on February 1,2010 | 12:48 AM

    My cells are for sale ! Need to provide me family a home before phasing out.

    Posted by khalil jamaluddin on February 1,2010 | 12:48 AM

    nice work

    Posted by preet on February 1,2010 | 12:48 AM

    wonderful story..this is yet another example of how Black people(and I am proud to say my people)have contributed so much to the world and in this case the lady never even got a chance to benefit from her contribution...(she didn't even know she was contributing) Kind if sad, isn't it?..I truly hope her family will some how be able to understand how important this is..GOD BLESS THEM

    Posted by jeri jackson on February 1,2010 | 12:48 AM

    Aa hah! Some good points for citation.

    Posted by Azaza Inal on February 1,2010 | 12:48 AM

    nice piece!!a very interesting topic..got pity to the family but was awed by their strength and courage to fight for what is theirs...tissue culture is a very important topic and issue of today!

    Posted by Juliene Dinopol on February 1,2010 | 12:48 AM

    i don't care for the way this article was finished. just dues are just dues. racial or not the big story is not the science however interesting and essential for what we've accomplished today. How dare you sell a part of someone duplicate and culture it without permission [microscopic or not]. the author just seems to be so thrilled with innovation. intriguing yet im turned off by final line of this article. grrrrr

    Posted by monica collins on February 1,2010 | 12:49 AM

    nothing much different from the story of erythromycin. where the "real" man-behind-the-curtain was put out of the limelight, uncredited and penniless.

    Posted by johnmar on February 1,2010 | 12:49 AM

    HeLa cells are amazing!! What is equally amazing is how much these cells have contributed to the advancement of science. Cloning, Polio vaccine, its astonishing how efficient these human cells are. It only reflects God's perfect creation. Gods ability surpasses all of sciences greatest efforts.

    Posted by Jonathan on February 1,2010 | 12:49 AM

    I, too, love this story. My mother died when she was twenty-six years old with cancer. I, myself was five years old. How I wish I could have known my mother. How many other human beings, have these "Immortal cells?." I will certainly find this book, soon.

    Posted by Lillie on February 1,2010 | 12:49 AM

    Wow!!! This is a great story. I would love to read the book with my family.

    Posted by Yvette on February 1,2010 | 12:50 AM

    Those are cancer cell they saved. Thats why they are still living ???

    Posted by Joyce on February 1,2010 | 12:50 AM

    Interesting article for me it enforced my thinking about the big differences in the way of thinking between both sexes, the daughter search for more information about her mothers while the sons' argument is to gain money! Husnia from Yemen

    Posted by Husnia Al-Kadri on February 1,2010 | 12:50 AM

    Normally diseased organs are incinerated or tossed away.
    What a great tribute to this young lady .... hopefully a cure was found for the cancer in her ovarian cells. Great story.

    THE MAKINGS OF A WONDERFUL MOVIE.

    Posted by Chuck on February 1,2010 | 12:50 AM

    In response to TM: The article is interesting but it makes me ask, are most people's cells so-called "immortal" and her cells were only available to science because they were taken without consent? ...or was it because it the cells were cancerous?

    Cell lines can be very difficult to grow. As we know now, different additives, food, antibiotics, and such can be added to the liquid the cells are grown in to help with it. As such, many different types of cells can be grown.

    The benefit of having a 'cancerous' cell line is twofold: (1) the cells grow faster, meaning you can do more research in less time (some cells will double in amount each day, others take much longer ... and you will need a certain quantity of cells to produce an appropriate response.) (2) if you are looking into drug research on a certain tumor, say for ovarian cancer, you will want to find a cell type that can potentially relate what you see in the 'plate' to what can occur in a human body.

    Posted by Kristen on February 1,2010 | 12:50 AM

    well scientists are also great creation of God. No matter how great are their works there is always an ULTIMATE SOURCE of all these. God creative work is on the process.

    Posted by lei on February 1,2010 | 12:50 AM

    This will be a very good book to read, I enjoy reading about peoples lives, how we become individual's of life. Thank you for focusing on what makes us people and not forgetting the people like Henrietta and her family.

    I can only hope to impact peoples lives like she is doing.

    Lisa

    Posted by Lisa Wilson on February 1,2010 | 12:50 AM

    Let's keep it real. Greedy white men have brought this country to it's knees. But some of you don't want to see that poor black family receive a penny for the unauthorized use of their mother's body. The world is again asking, are most americans depraved hypocrites. Thanks for a real history lesson for a change.

    Posted by Zeke Wms. on February 1,2010 | 12:50 AM

    nice work

    Posted by preet on February 1,2010 | 12:50 AM

    would love to get this book, I can see how much we can learn from it. not a science person, but the story behind makes it more attractive.. where do we get it?

    Posted by Raquel on February 1,2010 | 12:51 AM

    REALLLYY GOOD STORY ABOUT HER AND THE CELL,BUT THE DOCTERS SHOULD TELL THE FAMILY WHAT THEY REALLY WANT THE CELL FROM THE FAMILY.REALLY REALLY GOOD

    Posted by Floyd hashaway on February 1,2010 | 12:51 AM

    interesting article that proves what the bible says that humans were created to live forever but men has dominated men to his injury.Nice piece but, is it me or is everyone ignoring the fact that these ppl stole an unknowing womans body part without her concernt and are now trying to benefit? i wonder whose going to pay for that i bet they all think its of no imprtance anymore THE DOCTOR DID STEAL there is no other way to explain his behaviour...he shouldnt be awarded anythig for this find

    Posted by cocco on February 1,2010 | 12:51 AM

    How could this not be racist? Think of the syphilis testing on African American men...this is a common occurrence...It is apparent that her family should have notified of such discovery...her life was just important as anyone else. If her cells were that remarkable, then credit should be, and should have been rewarded where due. Thanks for submitting this story!

    Posted by TainoMari on February 1,2010 | 12:51 AM

    Well very interesting indeed! The Scientist didn't need to get permission to get the small tissue from Henriata anyway. Think of her refusing to give out that tissue, would have meant the strides that have been made in medical science could not have been realised instead. Yes it had to be from a black person after all many medical researches are conducted on what is perceived as less human by the white race for their benefits. God is great because the wisdom of a human being is foolishness. We thank God that the storry has been told about this heroin lady.

    Posted by Richard on February 1,2010 | 12:52 AM

    This is a very interesting investagative story. It is also a classic example of how the medical industry enriches some at the expense of uninformed, not necessarily poor and black, althtough Henrietta was both, citizens. Researchers steal your cells and probably mine, patent the lines and compensate no one but themselves. What do you think happens to all that unused medical waste from our medical tests???

    Posted by Lawrence Radford on February 1,2010 | 12:53 AM

    Can she be brought back to life some way(jurasic park)

    Posted by constance on February 1,2010 | 12:53 AM

    While reading the article,i just couldn't figure out if the story's ending is positive and can contribute goodness to humanity and glory to our Creator. The story is interesting because of the word "immortality" of a cells that has a cancerous disease. And as a Christian, everything that's going on in science world is still related God's Creation and Masterpiece. I can only conclude that it takes immortality to know the purpose of everything we discover.

    Posted by glen on February 1,2010 | 12:53 AM

    Regardless of the outcome, Henrietta was robbed of her cells without her or her family's consent. I highly doubt that they only became interested when they thought of the monetary aspect. It's obvious that Henrietta's husband was taken advantage of since it was made clear that he lacked understanding of the situation and only had a 3rd grad education. I see nothing wrong with the family wanting compensation-they deserve it.

    Posted by Kay on February 1,2010 | 12:54 AM

    A nice story. So many incredible things are discovered accidentally. I see so many thing here:brilliant minds, ethical problem, life desparity...

    Posted by wosene on February 1,2010 | 12:54 AM

    This is a very interesting aspect in science. Awesome. This is really for the good of mankind. But I am just afraid one day somebody makes a clone of Henrietta. What happens next? I am scared.

    Posted by EXAMINERAUTHOR on February 1,2010 | 12:54 AM

    from what I gather I am inclined to believe that since the culture was used without consent that they hid the fact../.they should receive a strong compensation...especially since it has helped many fortune 500 companies this America and it helped many American's especially from being infected with polio... don't forget how many people died or were paralyzed from that disease alone !!!

    Posted by Paul DeBarge on February 1,2010 | 12:55 AM

    Very good read. I definitely agree that the family should have been asked about donation before the cells were taken, but I disagree that the family is entitled to money. I agree with Jeanettes comment about the use of cancerous cells in vaccines. Who is to say that these cells wont produce cancerous cells in whatever research they are used in. I also think its naive to think that doctors and hospitals always inform a patient as to what is done with what they remove from your body.

    Posted by pam on February 1,2010 | 12:55 AM

    This is astounding. Why is this not common knowledge among even low-level science students? "HeLa" should be a household term!

    Posted by Kevin Davis on February 1,2010 | 12:55 AM

    Realy amazing story thanks to the writer

    Posted by A I Mursal on February 1,2010 | 12:55 AM

    What a shame the brothers had No interest in thier mother till they found out there was money involved. All of you who wrote in,JUST INTERESTED IN THE LOOT SHOULD BE ASSHAMED. When I here things like that I am truly asshamed to say YOU are from the same country as me. This poor young woman who died so young, probably saved you from POLIO & maybe other diseases and ALL you are interseted in is what you can hold in your hand. How terribly selfish. Don't you realize that's why this country is in such a mess? So many PEOPLE SITTING AROUND w/THEIR HANDS OUT, INSTEAD OF THEIR HEARTS WANTING TO HELP SOMEONE?

    Posted by Cathie on February 1,2010 | 12:56 AM

    Extremely interesting. Maybe now we can hope to have some great discovery to stop all the useless deaths from cancer. To my knowledge,there hasn't been any great outstanding finds to stop this deadly disease.
    INSULIN was discovered years ago, plus a cure for polio, and numerous other diseases cured. Very little money was available and they didn't have very many instruments for their usage, Now they have every type of machine, laboratories and thousands of scientists, working around the clock. Billions and billions of dollars, are spent on research, but still nothing. There must be some way of stopping this disease, but I am afraid, we are not being told the truth, as to how to stop this disgusting, deadly disease. Where is all the money going for all the extensive research??? THINK ABOUT ALL THE FUND RAISING that happens.
    WHERE IS THE MONEY REALLY GOING??

    Posted by Sylvie Brouillard on February 1,2010 | 12:56 AM

    I find it very interesting hardly anyone touched on the most important word in this wonderful piece, that is the word IMMORTAL. This is HUGE people, and please don't think for one moment the government or the elitist few haven't already known this information, it makes perfect sense they knew this information all along why else would there be so much focus on killing people of color..(racism) (slavery)......HMMMMM? It could very well be that this woman's genetic lineage is an open door to an end to disease, and possibly life extension for the human race. The government knows way more then what we've been told, and soon, this will be one of many 'FINDINGS" to help prepare humanity as a whole for the spiritual revolution that is and will be taking place on a massive level. ....they know that the gig is up that way too many people know what's really going on, so their disclosing information in dribs and drabs..... My eyes and heart are wide open. Real Eyes Realize Real Lies. Thanks for a great story! Namaste, Elaina

    Posted by Elaina Ewing on February 1,2010 | 12:57 AM

    A good one for history in the black month.

    Posted by Akinbo A. A. Cornerstone on February 1,2010 | 12:57 AM

    Where can I donate my own cells?
    It does seem that in it's way it IS immortality. Though the whole body may pass, those cells ARE immortal and can be a hope for the future!

    Posted by DLNELMS on February 1,2010 | 12:57 AM

    Without a doubt this is just another piece of American History untold because it does elavate the African American to a form of revelance. Thank you for telling the story. If it were not for researchers like yourself and Carter G Woodson, the African American history would stay hidden in Labs.

    Posted by Laura C Turner on February 1,2010 | 12:58 AM

    interesting story, is the book available in South Africa too, coz its a "must read!!!"...please let me know..

    Posted by Sihle M. on February 1,2010 | 12:58 AM

    I suppose the family would be entitled to some compensation, however, Lets deduct from that all the hours of research, flight costs, transfer costs, Medical costs involved with this research. Why is everyone so worried about money ?? For the Love of God ! If this Womans cells can save lives, isnt that compensation enuff ?

    Posted by Ozzy on February 1,2010 | 12:58 AM

    Fascinating! I'm amazed at all the responses here. Would like to read it as well. I have had african american kids as well as those born here of african immigrants in my piano studio for over 7 years. They have always been very respectful and hard working. They come from real nice families as well. As a young person in the military, I met all kinds of people and found many african americans to be quite the same. It's a SHAME that we are so color blind that we cannot see the good in those around us. It is my hope that more people will open their eyes to those around us everyday and pay attention to what is really important...a person's CHARACTER not their skin color!

    Posted by Cindy on February 1,2010 | 12:58 AM

    well, the medical world has employed gene patenting (which has been around for many years). donors are out of the money line. that's how it goes.

    Posted by johnmar on February 1,2010 | 12:58 AM

    Wow... amazing... immortal cells... this article was truely interesting... sounds like something out of a sci-fi movie.

    Posted by kayla on February 1,2010 | 12:58 AM

    Where can i buy a copy of this book here in the philippines?

    Posted by may on February 1,2010 | 12:59 AM

    This was such an amazing and touching story or rather factlines. They bring out HELa's cell so perfectly that u feel you understand every detail of science much as some of us are arts people. But really her family sh'd have been compensated on behalf of Henrietta Lack since her cells were taken without her knowledge and approval which was so cruel and mean of them really (those so scientists). But all in all her story is inspiring to the soul to know that HeLa cells are immortal.

    Was just wondering if this book is already down here in Uganda coz i would love to buy and read every bit of it.

    Posted by Susan Karungi Loise on February 1,2010 | 12:59 AM

    I'm curious as to why the doctor who extracted her tissue sample in the first place even decided to do it. Did he notice something different about her right away? Does this trait exist in other african americans?

    Posted by Selvokaz on February 1,2010 | 12:59 AM

    this story tell us that science is sometimes Good and sometimes bad but why science did not noticed? that the human biology is not really good? how come that they became Evil and involving many lives that innocent stop searching for pleasure!

    Posted by michael on February 1,2010 | 01:00 AM

    very interesting...well written.

    Posted by dipti on February 1,2010 | 01:00 AM

    were her kids ever tested? do they have the same cells? Did anyone ever consider that she may be a decendant of some sort of religious icon?

    Posted by z on February 1,2010 | 01:00 AM

    One of the things that people seem to be overlooking in this amazing story is that, given the geographic location, education, race, and socioeconomic status of the family, it is HIGHLY likely that they were/are extremely religious and would have thought the research to be immoral, ESPECIALLY in the 1950s. Also taking into account the family's mental/emotional state upon learning that their wife/mother had cancer, if they or Mrs. Lacks HAD been asked permission to use the cells, the answer likely would have been "No," and none of the advances we have made as a result of her cell line would exist. Keeping this in mind, some compensation is only just.

    Further, race was not likely the impetus for the doctor's and scientists' behaviors. But anyone who thinks that race wasn't at all a factor in this scenario (again, especially given the year and geographic location) is either extremely naive or willfully ignorant.

    Thanks for this incredible history lesson. Stories like these help to reframe the conversation surrounding scientific ethics and remind us that there is a history (or in this case, herstory) behind every advance that we make in our quest to improve the human condition.

    Posted by AC on February 1,2010 | 01:00 AM

    it goes to show you what are medical and pharma industry really thinks of us all. the yanomami are still fighting for their blood back that was taken from them. stealing is stealing. science is good so long as respect for the living subject be it a person, an animal or a cell comes first.

    Posted by sararagga on February 1,2010 | 01:00 AM

    wow!!
    thats an amazing piece of work..when i was studying tissue culture i was also intrigued by the HeLa cells..researched some but couldn't find one.
    u have done an excellent job..your book is a must read..congrts

    Posted by manu on February 1,2010 | 01:01 AM

    Everyone here would want to be compensated if this were their Mother. Not because of greed, but because it is fair. All of you who are trying to be noble and righteous should think twice before judging the sons for wanting what is rightfully theirs whether they worked hard for it or not,surely the wealth that most rich people enjoy was not won by the hard works of their own hands. As to the people who say that it was not their's to profit from and that they are greedy for money that other's worked hard for. Henrietta's cells were a gift from the creator and belonged to Henrietta and now via inheritance belong to her family. It is the same as you who are casting the stones are planning to leave your children your inheritance for which they did not work for...what's the difference? Henrietta had no idea they would be selling them and if she had known that there would be profit made, I am sure that sharing them with her family would have been part of the deal AND if she had neglected to make those arrangements,you who judge her family would have called her ignorant. And last,if there should be no compensation to the family because they should just be proud that it has helped many people, then shouldn't those who sold her cells have given of themselves just as freely and proudly? Someone will be getting paid for as long as Henrietta's cells live...over and over again, how noble is that? Money is the source neccessary to purchase what is needed for survival therefore it helps the human race just as the cells. Those cells represent fame and wealth for a lot of Scientist who do what they do with them and they should not be getting rich off what belongs to other people, thatwould be classified as Greed! WE ARE ALL THE SAME AND NO MATTER HOW HARD WE TRY TO PROVE ONE MORE WORTHY THAN THE OTHER, IT WILL NEVER BE...WE ARE ALL WORTHY OF THE TRUTH!

    Posted by T. Howard on February 1,2010 | 01:01 AM

    To the comments by Colleen regarding the cells not being immortal and that "everything that lives dies"; the phrase "immortalized" is specific to cell culture and more so to cancer or carcinoma-hybrid cells. As Henrieta suffered from cervical cancer, these cells grow as any cancerous cells would; They continue to proliferate without ever stopping. So long as these cells are passaged (harvested from culture flasks and re-seeded) or cryogenically frozen for storage (i.e. on liquid nitrogen)they will continue to grow on passage-after-passage; generation-after-generation.

    Posted by Matt H on February 1,2010 | 01:01 AM

    this study will surely contribute a lot in science and medicine. i hope the authority will protect and will use it for the development of our planet.

    Posted by thackhoy on February 1,2010 | 01:02 AM

    As usual the black men (her sons)have to be displayed as the evil ones, out for only money. Well I will speak out and say it's usually the other way around and this you can tell is by some chicks writting about a chick."well the daughter is trying to find history and the sons, they're just after money.) Please stop being bigots at least for the poor mothers sake. If you can't say something good about aome one then take the rest and shove it up your but author.
    And of course god bless the true america.

    Posted by on February 1,2010 | 01:02 AM

    Wow this is very interesting! Great job of tracing the real donor.

    Posted by Lyticia Vivianne on February 1,2010 | 01:02 AM

    wow, that was so fascinating and very intriguing!..it makes me want to purchase the book... :)
    i just love it...

    Posted by Ma. Antonette Grace T.Vista on February 1,2010 | 01:02 AM

    There is clear evidence that the family has to be compensated asap. If it was a white person's cells, no one would have thought twice about getting back to the POOR BLACK FAMILY a life to remember their loved one with, rather than reducing the relatives to samples of a laboratory.

    Posted by Kubukwena on February 1,2010 | 01:02 AM

    Yes, the family should get some compensation.

    Very interesting story.

    As someone who has been through ivf a few times and have children from it, it's interesting to wonder about cellular memory, cellular knowledge, even if diseased.

    Posted by Privacy on February 1,2010 | 01:03 AM

    is the girl who have the immortal cells still alive? will she never die? hmmpppp. i feel so curious. everything that has a life will soon be die.

    Posted by Mark David on February 1,2010 | 01:03 AM

    WHOA! THATS THE WONDER OF SCIENCE,AMAZING PIECE OF SCIENTIFIC FACT, DEAR LORD, JUSTIFY THESE WORK.

    Posted by JERRY E A on February 1,2010 | 01:03 AM

    did the family ever get any compensation, from the research, from this book??...and to Heaterman posted Feb 1 no we are all NOT just animals...

    Posted by no1uknow on February 1,2010 | 01:04 AM

    I think it is agreat development for science

    Posted by sharipur on February 1,2010 | 01:04 AM

    This is crazy.. I want to read this book..

    Posted by Johnson on February 1,2010 | 01:04 AM

    What an insult to not just Black persons, but to women!!

    The author has watered down what Mrs Lacks went through, and what her children must go through now.

    This is cut from the same cloth as what was done to the 399 Black men aka 'The Tuskegee Syphillis Experiments'.

    Hopefully Mrs Lacks' family will be able to get at least a monetary settlement.

    Since these cultures/tests were done after World War II, does this not fly in the face of the laws set down during the Nuremburg trials? I wonder if our champion journalist Ms. Skloot makes mention of this in her book/research?

    Posted by monkmalone@lycos.com on February 1,2010 | 01:04 AM

    God Bless you Rebecca and the family of Mrs.Lacks,your determination to find the truth is awesome!!!!I hope the family will benefit from this some way.

    Posted by Henry on February 1,2010 | 01:05 AM

    I see there must be a reason for everything we do.. amazing.....interesting to know deep inside ..cells that continously alive... no compensation...??????????

    Posted by frenze on February 1,2010 | 01:05 AM

    Those scientists are greedy and heartless. How can they enjoy that money alone while the family was in poverty.

    Posted by Moses on February 1,2010 | 01:05 AM

    Yeah, I got to know some new knowledge. As a Agriculture student I knew that we do plant tissue culture, bu I didn't worry much about animal cell cultures. Now I am curious about this subject.

    PLEASE, can anyone tell me are HELA cells the only kind of animal cells using in tissue(or cell) culture. Still didn't is possible to produce any kind of living cell culture by any other human ???

    I think as humans ALL OF US MUST show our greatest gratitude to Henrietta Lacks, as she has done a huge service even without knowing, for the good health of man kind

    Posted by Niranjan on February 1,2010 | 01:06 AM

    Great story! Hopefully the extended family can find solace in the fact that this normal every day lady who's life was tragically cut short has, and continues to do great things for the human race. Her legacy lives on. What a gift to all!
    Thank you

    Posted by Mark on February 1,2010 | 01:06 AM

    I am not surprised. I wonder who will ever admit that AIDS is a laboratory mistake that occurred when pharmaceutical companies used monkey plasma (which was later called "contaminated" plasma) replaced human plasma to manufactured polio vaccines. Of course Africa was "vaccinated" extensively with this in the 50's, which seems to correlate with the epidemic present today. Can you imagine the liability involved? Did manufacturing co disclose that monkey plasma had replaced human plasma in their vaccinations? Were their any concerns? Were they over looked? The need/desire to cure and the need/desire to secure equity is deep. I think the story is beautiful. Thanks Mrs. Lacks!

    Posted by ck on February 1,2010 | 01:07 AM

    Great "True Story", but remember the medical field is also about business; this was no mistake; those Scientist knew what they were doing. "Good Science"; I don't think so.

    Posted by Gary Faison` on February 1,2010 | 01:07 AM

    This is a facinating story. Only in America would the racial card be played. You can't apply current political standards in retrospect. In 1950 the whole question of ethical tissue sample removal had not even been raised. Doctors were taking samples from anyone and everyone, depending on their area of interest and work. The patient never missed the tissue. In the normal course of time, that tissue would have been died and been renewed within the persons body if they were alive and if deceased, it would have simple died. It would not even have occured to the doctor to ask permission to take a tissue sample. He wouldn't have asked had she been white, male or any other.

    This issue is detracting from the real story. How this woman's tissue has made our lives better. The tremendous impact the work done with her tissue has had on medicine. The marvel of how her minor contribution of a few tissue samples continues to enlighten and enrich our understanding of the complex and wonderful human body.

    Thank you Henrietta Lacks.

    Posted by karen on February 1,2010 | 01:07 AM

    I am moved to tears by this story. I cannot wait to read this book. What an amazing story!

    Posted by Kimberly on February 1,2010 | 01:07 AM

    What an awesome discovery of the contribution (although unwittlingly) by a BLACK WOMAN...

    Thank you for being so persistent in your research and in writing this story....

    Another star that help me shine with pride. More confirmation of being a part of a special people..

    Dolores

    Posted by Dolores Moore on February 1,2010 | 01:07 AM

    I was amazed to see all of the comments.. and that so many people were touched in some way by the story. What an enchanting story.. Also, this is such a hot biomedical ethics issue that will stir a lot of passion. I noticed that people are using today's thoughts and standards to respond so a situation that happened when laws, science, and knowledge were so different. That is very difficult to reconcile in my (our) minds. Seems there is unfairness in many ways; yet so much good came of the research. I will stay enchanted and look forward to the book and I agree, a movie could be next...

    Posted by Moxie on February 1,2010 | 01:08 AM

    Ok, so the doctors stole the cells, thats unethical. On top of that how much money has been made off of this woman?

    What if someone stole your cells and cloned pieces of you?

    Posted by Cell Thieves on February 1,2010 | 01:08 AM

    Cells are taken every day and sent to a lab so that there can be a cure found for what ails us. In turn we are healed and then maybe someone else can live because of us. Is this our way of life now, give us money, or is it give us life. But then again, some of us want compensation for living not realizing that God gave his Son Jesus Christ freely so that we may life. Just who do we owe?

    Posted by Robert e. Niblett, MOTAUSA on February 1,2010 | 01:08 AM

    So this would mean sometime in the future we will be able to live longer than the oldest person on earth. If a cell can live that long then a human can too. If they can find out how to do it that is. Crazy. Clones and then living forever. We are not GODS...

    Posted by shay on February 1,2010 | 01:09 AM

    People! These cells are the descendents of cancer cells that were taken from her tumour. They are "immortal" in the sense that they can divide indefinitely in a culture as long as conditions for cellular life are met. The individual cells aren't immortal; the author ought to have clarified that bit in the article.

    Posted by moonchild on February 1,2010 | 01:09 AM

    Great article! I love history and especially African American history. My interest has been peaked and I will buy this book. Thank you for sharing.
    dyah

    Posted by Dianna S. Johnson on February 1,2010 | 01:09 AM

    It is a hard job but it is fantastic that took almost a year even to convince Henrietta’s daughter, Deborah, to talk to you

    Posted by fawzi on February 1,2010 | 01:10 AM

    I took the time to read this artical and all the comments that followed. It still amazes me and makes me ashamed that there are those still out there that feel the need to make this a race issue. The world is not perfect and we still have a long ways to go. But with this kind of attitude we are not moving forward. This is a great and exciting step for all. And to make this into something other than recongnizing and remembering Hennrieta for her contribution and what she has done for all of us is just shamefull. We owe this women so much! Please don't belittle this womens accoplishments by turning this into something ugly. It's easy to find the bad in something but this is not what this is about! Let's all be glad that this is coming out to be recognized and how we can honor Hennrieta for her special contributions that she has made for all of us. A name to be sure that will go in history books to liveforever like her cells.

    Posted by Curtis Jones on February 1,2010 | 01:10 AM

    u cant tell me that if someone had take ur mother cell and made a billion dollars off them u wouldnt want to be pay u sitting that lie ,and criticise the family u must be white because when it come down to compensating black people for they trouble u people cannot stand it im not racist or anything ,but its make me sick to hear someone like u talk about welfair and the people on it.eveing if we had good job u would have something to say.

    Posted by willie a on February 1,2010 | 01:11 AM

    THE FAMILY SHOULD GET MILLIONIONS AND MILLIONS OF MONEY.
    ITS HUMAN RIGHTS VIOLATION TO TAKE SOMETHING FROM HUMAN BODY WITHOUT CONSENT!!!! FAMILY SHOULD BE COMPENSATED BY THE STATE!!!!!!

    Posted by AJ on February 1,2010 | 01:11 AM

    woow!what an interesting article.Good job.I can't wait 2 have the book.The family of this"great hero" need to be celebrated.

    Posted by dupsy on February 1,2010 | 01:11 AM

    This is one of the GODs miracle.

    Posted by Monet DT on February 1,2010 | 01:12 AM

    I am amazed at the people who are saying that the family should have been compensated and are making this about race. No one at the time knew that these cells were special. Had they asked Henrietta they maybe would have paid her a few dollars at the time and that would have been it. The money that is made off these cells now is from the work of scientists who are growing the cells. The fact that this woman's cells have had such a great affect on science should thrill her family, not make them greedy. I think this is an interesting story but I can't see why her family should be compensated for some microscopic cells taken from their mother. Be glad that your mother's life had true meaning and quit trying to sully it with money grubbing. Many "poor" people find a way out of poverty through hard work and education - maybe this family should have tried that before moaning about a few cells that someone else did a lot of work with.

    Posted by Jennifer on February 1,2010 | 01:12 AM

    I agree that the family of Henrietta should benefits from the profits made from the cells.. . .very interesting discovery. . .

    Posted by Lucy Sarmiento on February 1,2010 | 01:12 AM

    Cool Story,I like it

    Posted by neesha on February 1,2010 | 01:13 AM

    This was a great story. I mean I kind of feel bad for the family in a sense because they could have used some of that money. I am amazed though, the nature of science and how it can truly impact life. Reading this let's me know that we are all human and in that we could all have some kind of impact on each other. Such a great story to start off February. Thanks!!!!!

    Posted by Rita on February 1,2010 | 01:13 AM

    At the time the cells were taken there were no laws about informing patients. And they are not the original cells. The production of those cells was paid for by the scientists, not her family. If you buy a horse from someone, are it's foals yours or the original owners?

    Posted by Me on February 1,2010 | 01:14 AM

    wow, I have heard about the Hela cell line, But i did not know it had a very interesting story behind it.

    Posted by Kele on February 1,2010 | 01:14 AM

    Scient is objective not subjective the problems begings when we mixt them,but if every body do what is RIGHT the problem wouldn't exist;however we have to realize that this is the nature of our human being.CONGRATULATIONS to have the courage to publicate this story HURRAAAA for the TRUTH & SCIENT :sooner or later the truth will prevail.Please let me know how can I get this book.

    Posted by Francisco Granados on February 1,2010 | 01:14 AM

    I unlike most look passed the color issue that I see many have turned your story into. I think you have an amazing way to catch the reader, leaving the reader wanting more. I like the part about hoew you said her daughter never met her mother, but I must contridict that because she has met her mother in a way that most never get to experience. She may never have seen her face, but has seen the effects of her life and the gift of life her cells have given to many people. Thank you for giving me the chance to learn about another amazing person in history. And to te rest of the commenters on here who cares if she was black, white, yellow, or polka dot she was an angel who gave the gift of life to many.

    Posted by jtscorpio26 on February 1,2010 | 01:14 AM

    this story is like the story from filipino teleserye,toni gonzaga is the artist......i think they got the story of that women...

    Posted by grace magno on February 1,2010 | 01:15 AM

    I find seveal points to be the essence of the article.
    1. Defintely don't see the racial point of the donation as an issue. Seems to be one for those that don't grasp the true impact of her contribution. Don't understand the importance of the race card being played other than for entiltlemnet issues.
    2. Most scientific discoveries are serendipidous. They didn't know what the outcome woud be, they could only speculate that this could have some scientific benefit because of her medial history, and their speculation proved to be correct.
    3. HIPPA laws as we know them today were non-existent then.I don't see premeditated greed in here as much as others claim. I see forethought on the part of the researchers.
    4. If the family is compensated, the funds like a scholarship should have guidlines as to how they are used.
    5. What about the Jews in WWII- there were innumberable medical experiments taking place, and much was gained on many levels.
    6. what about persons who donate their bodies to science. Are their families compensated for any future findings that may benefit mankind?
    7. Truly, through accident or serendipity, this lady ended up having some genetic outcomes that benefited mankind. I think that in our current age, if we need to include compensation in the research paradigm, it should be spelled out ahead of time. One idea or finding will usually stimulate the mind or research protocals for others, which can lead to greater benefits that were not originally targeted. If a person agrees to participate in a research study, and need compensation, spell it out in the beginning, and let the outcome find its own reward. I think most people can find value in altruism. That human element exists in all of us regardless of our educational level. It just isn't always expressed.

    Posted by Lori Salinas on February 1,2010 | 01:15 AM

    This is a good story to start the day. Hela cells helps as a lot but also because of the genius scientist, but giving a little to the family of Hela is much better. This cell is important so better think for the family for further help in the near future.

    Posted by LadyM on February 1,2010 | 01:15 AM

    Well you have to understand that man was originally created to live forever... and sense we know that genes are passed down through generations, it stands to reason that some of thous original cells would be passed down as well. Believe what you want but the facts are facts.

    Posted by Wamara J on February 1,2010 | 01:15 AM

    WoW!! Wonderful!! Proof...that when God created humans..it was meant to be forever, because our cells DON'T DIE.
    one more vindication for true Christianity. Thanks a mill...

    Posted by juliana80808 on February 1,2010 | 01:15 AM

    Truly a very inspiring story which really moves me.. it is as if she becomes an immortal contribution to scientific breakthroughs. i hope her essence would be given credit by even giving her family a decent way of living as a form of gratitude to that contribution.

    Posted by Arnold Alderite on February 1,2010 | 01:16 AM

    "The people behind those samples often have their own thoughts and feelings about what should happen to their tissues, but they’re usually left out of the equation." This is not true anymore. At least, it is against federal law to do that.

    "They knew that they could get away from "stealing her cells" because she was black. Back in the 1950s something like this was just swept under the rug; no one would have ever believe that a black woman cells could have a major impact in medicine several years later. The scientists should have at least consulted with the family, informing them that we took some of your family's cells."???

    Back then, it was typical to take samples to try and grow anything. It didn't matter who it was from. And yes, there has been experimentation on prisoners, soldiers, and orphans in the past. If you want to read what the rules and regulations say now - see the Office of Human Research Protections in the Dept of Health and Human Services. www.hhs.gov/ohrp/. It will describe all of the legislation that is now in effect as well as document the history leading up to the development of these protections.

    It indeed is unethical in this day and age to take anything from a person (volunteer, patient, subject) without their consent - even their answers to questions for research purposes. That is what institutional review boards are for. This is nothing new - sounds like the author isn't really familiar with some of what she is writing about. Or at least, the article suggests this is some plot scientists and researchers have to steal peoples body parts for the sake of science. It is not true.

    Posted by kristin on February 1,2010 | 01:16 AM

    The cancer's cells usually are growing and never dying, that know the doctors.

    Posted by gabriela on February 1,2010 | 01:16 AM

    I just checked on amazon.com and it said that "The Immortal Life of Henrietta Lacks" will be available in KINDLE edition tomorrow, February 2, 2010. How about the hardcopy (paperback/hardback cover)?

    The article written here made the book sound very interesting. It sounds like one of those books you read, and all of a sudden makes you think about Humanity (human-nature: selfishness, care for mankind, greed, success, triumph, etc.). I am so looking forward in reading this book... I'm hoping the book actually lives up my great expectations... =)

    Posted by Mary on February 1,2010 | 01:17 AM

    Thank you so much Sarah, for opening up my eyes to such a provactive story. This is truly an exceptional biography that seems to be long overdue in informing today's society of the intruencies of medicine from back when.

    I look forward to the reading of "The Immortal Life of Henrietta Lack", and I will definitely have my eyes open for this one!

    Best Regards,

    Posted by Chloe Collins on February 1,2010 | 01:17 AM

    This is an mazing story. Is the book available in Kenya? It is a must read piece. Congratulations to the writer.

    Alloys Omolo
    Food for the Hungry Association, Pemba Mozambique

    Posted by Omolo Alloys on February 1,2010 | 01:17 AM

    Wow! This definately caught my interest. I'm putting this in my list of books to buy.

    Posted by jahjah on February 1,2010 | 01:17 AM

    I have donated my body to science eventhough my cremation is pre- paid. whatever can be given or done to help the living after we are gone should be payment enough. Too many people die and waste so much that can continue living in the living. Such greed. Wish there were a law that d required the recycling of us all. Just knowing that we are contributing to humanity would probably propel our spirit to a good place.

    Posted by Anelsie on February 1,2010 | 01:17 AM

    I found the excerpt to be very interesting and informative. I would be interested in reading the book, if only to validate my theory about the side effects of racism and poverty. The author defends the scientist who took the cells of a poor Black Female without her knowledge as not being racist. Maybe he was or maybe he wasn't, but his actions were; only minorities and the disadvantage are exploited without consent and: the outcome was: a family left in poverty without recourse, while the scientist his colleagues and the university he worked for become wealthy off the live cells of their dead wife and mother. It seems to me if the author was sensitive to the needs of the family instead of the needs of the scientific community, he would have realized something was not right when they continued to change the name of the mother to keep people from learning who she was. But of course that is okay because the Family was Black and poor and would not know what to do with the money if they received any. Only writers and scientist should have money and fame because they know what to do with it. Shame on you and the scientific community who took and is still taking advantage of this Lady and her Family without giving them the notoriety and the wealth that should have come with it. Don't you think that she wanted her Family to live a prosperous life, children growing up in a nice home having the opportunity to go to college and live a successfull life or did you think she was not human enough to have aspirations for her family.

    Lee Jenkins

    Posted by Lee Walter Jenkins on February 1,2010 | 01:17 AM

    Money. Money. Money. Unfortunately, that is all some people care about and do evil things. My mom and dad wrote their will, so that their remains would be donated to science. Years later we found out that evil people had sold their body parts on the black market for profit and not for research as intended. We even got money in the collective law suit settlement which we donated to the poor. I am now afraid to donate my body to science, as I had intended before this horrible thing. It's sad that we think all scientists and doctors are good. They are human too and sometimes do bad things.

    Posted by Michelle on February 1,2010 | 01:17 AM

    EXCELLENT ARTICLE! THIS TYPE OF INFORMATION SHOULD TRULY HELP MOTIVATE MANY INDIVIDUALS TO HAVING FAITH IN DISCOVERING THE SECRETS OF GENITICS AND HOPE FOR THE FUTURE!

    Posted by Robert Filz on February 1,2010 | 01:17 AM

    Great story and it definitely has something to do with money HL's family should get some compesantion, if the medical fraternity made money from it why not the family, thumbs up for HL.I would buy the book

    Posted by Deliwe on February 1,2010 | 01:18 AM

    What a an amazing story and i was so fervent when i read it and i am still waiting to read the rest of the book.is it aready on sale or not yet? tanx for this amazing true story.

    Posted by temesgen on February 1,2010 | 01:18 AM

    Black is not only beautiful, it is also amazing!!

    Posted by edvi on February 1,2010 | 01:18 AM

    MMMMM... yeah this is ineed insteresting in the fact that I did like hearing what all was done with her cells, I also wonder about compensation for family. But the writing of this article was HORRIBLE!!!! First, everyone knows deseased cancer cells are longer living and have different properties from normal cells they are not immortal. Secondly, if the immortal was refering to their use, ok, but it also sounds like this author is trying to say "she was there for the polo vaccine, she was there for the space experiments, she was there for cloning", she wasn't!!!! This woman had nothing to do with any of those things which other people spent their entire lives, working to do and create. It was her cells thats all. None of her, she provided no imput or work into any of those acheivements.

    Posted by Sally on February 1,2010 | 01:18 AM

    very interesting article. I feel pity for her family. The government should help them.

    Posted by lenie creus on February 1,2010 | 01:19 AM

    After reading the comments, I've been amazed how this issued has mutated into money and race. Yes, perhaps there have been miraculous breakthroughs with this HeLa's cells but how many scientists do you know who are actually rich? Very few. And how many people want to cash in on their dead mamas? Very few?

    Get it straight. That was then; this is now. Did Henrietta ever pay for her treatment at John Hopkins? Is everybody really sure it was white-as-snow, male researches who so "misrespectfully" took her cells? Scientists just look at the data and the research. Is there any chance these money-grubbing heirs could just be proud of their mom? Probably not if their $$$ involved. Seems like a case of 'I'm going to cash in."
    S

    Posted by cd on February 1,2010 | 01:19 AM

    Very enlightening! If there is money being made in this thing then some should go to that poor family. Have a heart and pay up greedy. Someone help them get a good lawyer!

    Posted by clara on February 1,2010 | 01:19 AM

    I was just wondering if the piece of tissue from her tumor was used would that mean that they were using cancerous cells in all their experiments? Or was it just healthy tissue from her body that was used? Any way this was very interesting.

    Posted by Lori on February 1,2010 | 01:19 AM

    wow! the story is indeed fascinating! i love reading about science and the mysteries it tells. I hope to have acopy of this book, is this available in the Philippines?

    Posted by Caroleen ileto on February 1,2010 | 01:19 AM

    Wow amazing history!

    Posted by tmatan on February 1,2010 | 01:19 AM

    From what I've read about Henrietta is she was a generous woman. Her cancer was biopsied and used for later study---as has happened with many other patients who have had abnormal growths, no matter what their race. She was given what was felt the most up to date medical attention at the time...but lets face it, in 1950, cancer was still just about a death sentence. If it couldn't all be removed with surgery, the patient didn't stand a chance. She was not used or misused...she died of cancer and the doctors studied the cells...as they did with many other patients' cells. Hers just happened to have the potential to replicate and survive. I doubt the researchers even knew she was black or even cared. They were simply cells to be studied and their hard work resulted in the medical advances that came of it. Please understand---when the cells were sampled, it was not with the idea that money was going to be made. No one had any inkling that would ever, ever happen.
    To the person who asked how Henrietta died--her body was riddled with cancer, with tumors growing everywhere. The cancer destroyed her kidneys and she technically died of uremic poisoning, as a result of the effects of the cancer.
    It was very awful and tragic--but some good came of it.

    And no, the husband does not deserve any compensation. When you read the book, you'll find he was not a "stellar" guy.

    Posted by Les on February 1,2010 | 01:20 AM

    Why the concern about monitary compensation for the family? They didn't own the tissue. It wasn't willed to them. Diseased tissue, is removed from thousands of people every day, and nobody cares, what happens to it. Some is used for medical reasons and some is thrown out. Its not STOLEN.

    Posted by Shar'le on February 1,2010 | 01:20 AM

    To some of those who say that Henrietta Lack had not done anything significant in her life to deserve compensation, I'd say that you are being at the very least disengenious and at most grievously disrespectful of her special rarity. The way that some of you verbally minimized her unwitting contribution to our quality of life hints at disdain or even hate. Why are some of you trying to reduce her to the value of a lab rat? How would you characterize all of the blue-blooded royalty in europe and for that matter, the obscenely rich children of old american dynasties? As far as I'm concerned, they have not contributed anything unique to our society's enrichment, yet they are not villified as having no intrinsic value. Simply being born into power and money makes you valuable, I guess.
    Suppose what would happen if a Vanderbilt or a Rockerfeller was born with such unique cells. Bet your bottom dollar, they and the entire family would be richly compensated and none of you villifiers would object. Their lawyers would make sure that billions of dollars would change hands for the use of those cells!!! We should be thanking Henrietta Lack for the possibility that her cells provided the means for our continued existance. No doctor, researcher or scientist up to that point in time or since that moment was able to keep any other line of cells dividing indefinitely. No one has ever been able to repeat that feat with any other human being. Henrietta never did anything significant in her life? Without this particular woman, the scientists and researchers would have absolutely nothing to help them make the myriad of discoveries, medical breakthroughs, vaccines and cures. Without Henrietta, some of you might not even be alive. Can you, in your strangely myopic way, realize how many people's lives she has saved or enriched?

    Posted by Marge on February 1,2010 | 01:20 AM

    Scientist playing god how about that. I am interested on reading more about this family and the book. More interested in the family than the cells. If she had cervical cancer back then how come we still don't have a cure for it. Isn't cervical cancer hpv now!

    Posted by Theresa Brooks on February 1,2010 | 01:21 AM

    Henrietta Lacks should be suitably rewarded by scientific community with a memorable prize if not Nobel posthmously.

    Posted by Prof. A.P. Garg on February 1,2010 | 01:22 AM

    So what about the money???? The study of Ms. Lacks' cells has furthered scientific and medical knowledge by leaps and bounds....wouldn't have happened if that doctor hadn't taken a piece of the tumor and given it to a scientist.

    And yes, I'm definitely buying the book. I'm interested in Henrietta Lacks' story not just from a medical standpoint but from a sociological one as well.

    Posted by Susie on February 1,2010 | 01:22 AM

    My bad, amazon.com also offers a hardcover version of the book.. It's worth $14.04 as of February 1, 2010 10:22 PM.

    Posted by Mary on February 1,2010 | 01:22 AM

    I think the family must be compensated somehow financially. That would be the right thing to do.

    Posted by Miket on February 1,2010 | 01:23 AM

    Very interesting,I am sorry I can not find this book in Romania.Congratulations to Rebecca Skloot. Even now,the human body is still a mystery!

    Posted by Gigi M. on February 1,2010 | 01:23 AM

    What is a shame is how many comments I've read from people thinking that this family should get money from... whom? Should we all give a $1 if we got a polio vaccine? Get real, people. Henrietta's doctor had no idea that his colleague's experiment would lead where it did -- NO ONE could have known that her cells would be able to replicated for decades, nor what experiments would be run with them, nor what the outcomes of those experiments would bring to humanity. It is these researchers, their companies, and the many hours of work done by scientists who rightfully made and deserve to have made the money. Neither Henrietta nor her husband would have understood what "permission" they were giving had they been asked if her cells could be examined. If the experiment had discovered a cure for cervical cancer that saved Henrietta's life, would they have been asking HOW that happened? No, they'd have assumed it was God's will. Well, in the same way it was God's will that her cells were used to help humanity. Her sons and daughter have no claim to make in this scenario. No intentional injustice was done to H. L. or her family. Why is everyone always so quick to want to sue someone? As if every cog in a wheel of discovery should be PAID for it's part! The only people who should be paid are the ones who spent hours in the lab doing experiment after experiment until something useful FINALLY happened... and the companies that then took that discovery to the masses in the form of polio vaccines and other miracle drugs.

    Posted by Not Entitled on February 1,2010 | 01:23 AM

    Great story. And, by the way, what a gorgeous woman Henrietta Lacks was. Perhaps beauty is immortal.

    Posted by ParkRow Pioneer on February 1,2010 | 01:23 AM

    There's a lot of discussion here based on incorrect information. First, an "immortal" cell is not a cell that lives forever, it means that the cell can keep making exact copies of itself if it is in the right environment, such as in a cell culture. This is why cancer is so devastating because it just keeps on reproducing and doesn't stop until the environment is destroyed which is sadly the human body.

    Second, while it is clearly wrong that the scientists did not get informed consent from the patient, it was not due to racial issues. In the 1950's informed consent laws simply did not exist - anyone could have been subject to having their tissue sampled irregardless of their ethnicity or economic status. Someone stated that because this women was black, you are only hearing about this now. Have you ever heard of Frances Mallon? She was a woman from which breast cancer cells were taken to create another immortal cell line for science and research. She's white and hardly as well known as Henrietta Lacks.

    Third, it is not unethical for the family not to have been compensated. No part of your body, with the exception of blood, semen, egg, and hair, can be paid for otherwise you would create a business of selling body parts. Think about it... it would be even more unethical to be compensated for your tissue because it would create a market that would prey upon the very people that you want to protect: the poor. What kind of society would we be in if a person could sell his arm just to pay his bills?

    Finally, while companies have benefited from the use of the cells to create new and more effective drugs for cancer treatment, the cells themselves were never patented and so anyone is free to use them which means that no one has ever made a profit on the selling of these cells.

    I know the media needs to make articles interesting to sell them but this kind of journalism just inflames people without giving the full story.

    Posted by ConcernedScientist on February 1,2010 | 01:24 AM

    Loved this story. I will have to get the book. I think this would make a great Movie! Also, I think her family should receive money from the sale of the book or movie. She was a beautiful lady. Live on cells of Henrietta!

    Posted by Stacey Blackwell on February 1,2010 | 01:24 AM

    AWSOME!

    Posted by Crystal on February 1,2010 | 01:24 AM

    Taking cells from a tumor without someones "permission"? She gave them "permission" by having them treat her in the first place. Doctors always take samples as a means to treat the patient and to do research for future patients. How many other cells were taken without "permission" from others? likely thousands. Would she have said No if he asked her? I say no!

    Posted by Thomas on February 1,2010 | 01:24 AM

    This is interesting! Though there maybe some human rights violation that happened earlier when Hela cell was taken, it has tremendously helped humans stay alive. But then again, the family deserves to be well compensated... after all it's their mother's.

    Posted by sponge on February 1,2010 | 01:25 AM

    The story didn't fully answer the hanging question of whether it was morally right for Henrietta not to have received recognition or monetary compensation. Maybe the book answers the question in more detail. In fairness to the initial scientists, when Henrietta's cells were taken, I'm sure they weren't readily sold on the black market. The cells were dissected/grown/re-manufactured at great costs and work with more failures chalked up than successes. In the case of HeLa cells, the scientists found a viable cell sample. The question arises whether grown cells are in the same category of cloned cells. When do people lose legal ownership of their biological material? Are current cells significantly different from first generation HeLa cells? Are aborted fetuses considered living tissues or human beings used for stem cell research? As the author states, medical research depend heavily on tissue culture; society in general benefits from the scientific research, even HeLa's descendants.

    Posted by bobe on February 1,2010 | 01:25 AM

    aren't all cancer cell lines "immortal"? I mean, take cells from cervical cancer, prostate cancer, skin cancer...they are all considered immortal, right? And we can preserve them indefinitely. Why is this a story??

    Posted by John on February 1,2010 | 01:26 AM

    The family doesn't deserve a payout just because they are dirt poor. It was the scientist that used a biopsied piece of tissue that made it have any value past a piece of trash.
    The lottery mentality of our society is sickening. All about money for nothing.

    I wonder how much the original doctors were compensated by the family for the medical services for Henrietta? I bet the family didn't pay zip! Opportunists...

    Posted by greg on February 1,2010 | 01:26 AM

    good!

    Posted by GEROME UY on February 1,2010 | 01:26 AM

    I remembered the story about some cells that found their way into places that they were not suppose to be and that it actually was causing problems for the scientist doing research on cells not pertaining to this woman. I hope they are not using her cells to make any thing that is to go into humans because they are cancer cells. Some cancers are caused by viruses Cervical especially. Maybe the Author of this book would be willing to share a portion of the proceeds to this womans poor family. Making sure that money goes to teaching them all to read.

    Posted by Roxanne on February 1,2010 | 01:26 AM

    this is really amazing how science has been able to freeze tissue cells in an effort to find a cure,for some of these sickness that has occur through the ages.no her family shouldn't be entitle to anything,if it hadn't been for indepth studies and someone trying to find out the real story behind henrietta lack they still wouldn't have known.money can sure change people.they should be glad that whether it seems like it.that was her contribution to society.thank you so much.Mrs.Henrietta Lack

    Posted by virginia robertson on February 1,2010 | 01:26 AM

    Are you going to compensate the family with the earnings of your book? I think it will be fair and good public relations.

    Posted by X1MXM on February 1,2010 | 01:26 AM

    Well, thats great.
    This is typical of biological work.
    Keep on doing experiments using human tissues.However, be very careful because cloning may result into individuals who may have totaly different thoughts from yours and mine, and may end up destroying all of us.Thats vampire like phenomena.Need to do with caution.

    Posted by marto on February 1,2010 | 01:27 AM

    How many of MY cells were used for scientific research and will *I* be compensated? If you compensate one family, you have to compensate them all and not only is that NOT responsible, but it's also not feasible. The identity of the cells wasn't meant to be discovered; thus, their using only the first two letters of her names to identify the cells. As nice as it sounds, it's just not possible to pay the family for her contribution to society. The most they SHOULD hope for, and possibly pursue in her interest, is a medical affirmation in the way of a plague. Or maybe even have a hospital or a research center or something being named after her to immortalize her. You can't pay money for something so monumental! If so, then where do you stop?

    Posted by Chris F. on February 1,2010 | 01:28 AM

    what could we do to help this family get paid????? Great article and I will definitly by the book because your interest in the story really makes the book worth buying. Please share the proceeds with the daughter at least.

    Posted by yvonne on February 1,2010 | 01:28 AM

    Great story ever. I'm a pre-medicine student and is so curious about learning the story. Might as well read the book! Cheers!

    Posted by Charm on February 1,2010 | 01:28 AM

    Just confirming what the rest of the world already knows. Science is pinioned by a chain of reasoning and that is how it should be, but women hold the secret of life without any training at all!

    Posted by on February 1,2010 | 01:28 AM

    Could someone tell me why her cells are immortal?

    Posted by fatih on February 1,2010 | 01:30 AM

    Very interesting!!.. but how about the family??.
    very freakish! yet interesting.. :D

    Posted by Bao-et on February 1,2010 | 01:30 AM

    ..is this for real?!..i was amaze that i didn't hear it until this moment!?..i'm excited on the book..

    Posted by Rhea on February 1,2010 | 01:30 AM

    Never too late to learn.Iam a BIOLOGY MAJOR FROM THE LATE 50s-EARLY 60s ATTENDING AN HBCU.THIS COULD HAVE BEEN A GREAT INSPIRATION FOR ME.WAS ALSO A POOR TOBACCO FARMER.

    Posted by dr.f.baker on February 1,2010 | 01:30 AM

    awesome stoery.i am not much into science,but this is very intereting.i would buy the book.

    Posted by karen on February 1,2010 | 01:30 AM

    So the cells of a woman with cancer were used for vaccins and many other things used to inject in the human body. Am I the only one wondering whether this is why cancer has gotten to epidemic proportions in the western world?

    Posted by consciousscience on February 1,2010 | 01:31 AM

    if the parent have that kind of gene..would it be possible that their children could have it too...would they ???i mean are they..???

    Posted by Dee Jay on February 1,2010 | 01:31 AM

    immortal cells its interesting ........ i want know if there is any research going on about this immortal cells......and is there any journal about these cells.....

    Posted by abhijit on February 1,2010 | 01:31 AM

    Thanks Hela,all children in protection against polio owes it all to you.May your soul rest in peace for a big reward awaits you in heaven.To the scientist behind all these,big ups!The only place you went wrong,not not letting Hela's family members on this one..........but do I say?

    Posted by Jack Teddy on February 1,2010 | 01:32 AM

    It is a true evidence Indeed, and it is a wake up call to those who don't believe The life after death. The mystery of the creation and the beleive of the creator of the universe from Cell to human life. waaw we'll hear more from that perspective theory.

    Posted by Abdi on February 1,2010 | 01:32 AM

    This is very interesting book...

    For century and years, human beings are being used in the lbaoratory without their knowledge. I just hope a proper compensation will be given to her family...

    GREAT WORK Rebecca...

    Posted by Maya on February 1,2010 | 01:32 AM

    This is another story about using someone as an experiment . I know that during the 30's , 40's and 50's they used many black people in different experiment like labortory mice to test many different dieases and at what stages bad or good as the susscum to death and if they lived how there lived there lives if the made it to live longer lives.This is very sad and her family should be compisaded for all the good that has come out of this after they grew up without there mother.This is no surprise that this was done without her knowlage becouse they probally made millions sending her cells all over the place. This is clearly a breach between Dr. and pataint and also her constitusional rights. I hope the family and her children sue the snot out of them. God Bless her husband and children and the rest of her desendence.

    Posted by Betty Unnasch on February 1,2010 | 01:32 AM

    This is a wonderful story that shows the impact of an individual and also a black people and their impact on inventions throughout the years, most of which were erased or not mentioned. This is a wonderful story for black history month and a wonderful mysterious scientific adventure for future medical students and class room students whose minds can be probed to investigate why this great woman who have contributed decades of advances to medicine cells did not die.

    Posted by Marvin on February 1,2010 | 01:32 AM

    i am a medical technologist and for the 4 years of being in the school, we just have talked about HeLa cells. and it's my first time to know where the HeLa cells came from and what it really means... it's an amazing article and i hope you can post more articles bout it... GREAT JOB!

    Posted by digna bernardino on February 1,2010 | 01:33 AM

    its simple amazing and mind boggling story.i appreciate the research work that has been done and salute the gorgeous lady who saved many lives

    Posted by zafar iqbal sandhu on February 1,2010 | 01:33 AM

    wow! this story is unbelievable..i've never imagined about a person having immortal cells in his body..i'd like to have a copy of this book..really interesting..

    Posted by jade on February 1,2010 | 01:34 AM

    I was facinated by this story. I feel that if they were my families cells used to "breakthrough" and aid those that are suffering then by all means, do it. I excpect nothing monitarily and hope to save anothers life as payment enough. What our society has become is scarry, you have to be so ridiculously diverse that we can't even find suttle ways to say, do or excpress anything anymore. Just find a cure and those who feel they have something comming to them,earn what you can and be happy with yourself and your achivements alone. Please stand on your own two feet and help the world. Don't excpect the world to help you all the time. I am happy for Mrs. Lacks contribution as I am sure all she would want is to make a difference to save others.
    Thank you,
    PD

    Posted by PD on February 1,2010 | 01:35 AM

    WHAT AN AMAZING STORY, BUT I FEEL THAT WITH THIS TAKING PLACE IN 1951 THIS DOCTOR WAS HARVESTING THESE CELLS FOR THE FUTURE HEALTH GAINS OF HIS WHITE RACE HE DIDN'T CONSULT WITH HER HUSBAND AND LET HIM KNOW BECAUSE HIS RUSH WAS NOT TO PROLONG HER LIFE OR HER CHILDREN LIFE ,BUT GOD GETS THE GLORY BECAUSE IT HEPLED ALL PEOPLE AND ITS STILL HEPLING IN RESEARCH ,THIS WAS BAD MEDICAL ETHIC BLANE AND SIMPLE AND WITHOUT THE HELA COMPONENT TO THESE VARIOUS RESEACHES THEY WOULD NOT HAVE BEEN SO SUCCESSFUL SO "COMPENSATE THIS FAMILY THEY COULD HAVE RECIEVED AND EDUCATION AND HAD A BETTER LIFE IF THE RIGHT THING WAS DONE FROM THE START ,ONCE AGAIN IT PROVE THOSE ANCESTORS OF OUR BLACK PEOPLE WERE A STRONG PEOPLE WHOSE BODIES LEARN TO HEAL THY SELF AND STAY STRONG

    Posted by elaine on February 1,2010 | 01:35 AM

    It merits to ponder.

    Posted by m. forouzanfar on February 1,2010 | 01:36 AM

    Did anyone else notice that the writing style is kind of juvenile. Sort of like the level of a piece written for the National Inquirer. You know written by a kind of "hack"?

    The story is interesting though - just would have been better in someone else's hands.

    Posted by Dave T on February 1,2010 | 01:36 AM

    Loved the article. However, there was an underlying tone that disturbed me a bit but I couldn't put my finger on it untill I read a post by "Smith Feb.1,2010/ 12:40 p.m." That is what bothered me, the "label" As you penning this very interesting story, I really am surprised you didn't choose a less demeaning description of Mrs. Lack.

    Posted by Gary C. on February 1,2010 | 01:36 AM

    I like the story but hard to believe. Anyway the contribution is enormous to our scientific world. Thanks to Henrietta Lacks let the Almighty bless her.

    Posted by Abebaw G on February 1,2010 | 01:36 AM

    if her cells used to cure people then she is a hero.

    Posted by Edward Mendoza on February 1,2010 | 01:36 AM

    Wow this story realy moved me , an im going to buy the book.

    Posted by Kamal Johnson on February 1,2010 | 01:36 AM

    Truly an excellent article and I will read the book. For the last 30 years, I have known about HeLa cells and their use in science. I am glad now to know more of the story about the donor's life. Does anyone know how to petition the Nobel Committee so that Henrietta Lacks should receive a Post-humous Nobel Peace or Science award? Contact me if you do.

    Posted by Carrie A. Chism Delaney RN BSN on February 1,2010 | 01:37 AM

    yes! its very interesting! as a read it and put my self on one of the characters my feelings is "angry"! i hate those scientists that thinks only their selves. even though she is immortal or have that cancer still she's a human that needs love and live peacefully in this world, they shouldn't treat her like that!if i were one of her daughters i will take the scientists to jail, for what they do to my mother.! they should pay a debt to the prison!!!!!!!!!!

    to the scientists:

    think of every move you make, it doesn't mean that you can do whatever you want to do in the field of science because you are a scientists. thinks what is the come up and think what somebody thinks of it and anyone feel about it.! think of many times before you do such things.!!!

    Posted by conny on February 1,2010 | 01:37 AM

    it was a great story, a true to life story that what a human can do. in fact this is reality, people with power and brains takes advantage to all un-educated and poor people, they just treat them as not a human being, they dont care anything. all they care about is they're fame, in this book i know many who can read this will absolutely learn that "PEOPLE ARE NOT A GENEA PIG".

    Posted by khriztope on February 1,2010 | 01:37 AM

    I do think the scientist should have asked Henrietta to take her cells, but at the same time she must have been undergoing some kind of procedure that involved removing a sample of the cells. I dont think he bumped into her at the super market and started scratching away at her. At the same time people donate or sell there cells to research all the time and if your cells go up to space or are used in creating a vaccine that ends up selling over $10 billion of vaccinations, I dont feel like anyone owes you a percentage of that. That money should go to further research or to assist in creating and distributing that vaccination so it can benefit everyone. Everyone has cells, its coincidental if yours are used.

    Posted by Nene on February 1,2010 | 01:37 AM

    She's a beautiful lady. I don't understand why her cells were used for so many purposes vs. using fresh cells from different people. Unfortunately, it sounds like some of her ancestors are not the sharpest tools in the shed. I wouldn't be surprised if those children who were uninterested in their mother, until money was involved, wouldn't just squander away whatever they are paid. I'd like to see the daughter get some money because she actually cared about her mother.

    Posted by Lindy on February 1,2010 | 01:38 AM

    very interesting story, i will buy the book, but a sad state, that almost everyone with a coment wants to know if they got money! isn't there anything more important than receving money for something? i would hope so.

    Posted by Harold on February 1,2010 | 01:38 AM

    I feel God used those scientist to discover Hela, and as Jesus played his part on earth, so Henrietha is still playing her's. May God bless her

    Posted by Obende Uje Lloyd on February 1,2010 | 01:39 AM

    I am truly touched by this story! Henrietta should be in science books and children and adults should know her name! She has a place in history and her and her family deserve to be recongonized for the things they were able to achieve by using Henrietta's cells. Its sad to say being an African American woman this is the first I have ever heard of Henrietta and her contribution to histroy but I know it will not be the last! Please continue to educate people.

    Posted by Sasha on February 1,2010 | 01:41 AM

    I am sure that this happens all the time. It has helped research but the family that is only in it for the money doesn't deserve any. The husband and daughter should recieve some but probably never will.

    Posted by Bambi on February 1,2010 | 01:41 AM

    oh my GOD

    Posted by iman khatami on February 1,2010 | 01:41 AM

    It's a wonderful research. I really want to have a copy of the book. Is the book out in the market? May I know the title of the book?

    Posted by jox on February 1,2010 | 01:42 AM

    Your story is not only educational but very up lifting.I am very pleased that research has come so far. Our whole future depends upon this kind of scientific research.

    Posted by Abida Sultana on February 1,2010 | 01:42 AM

    The family should be compensated and a good reason for health care for all. You use a black woman to heal a sickness at the time was killing off white people left and right and yes keep it from the family. When you find the vaccine that can help half of todays sick people in 3rd world countries most of them people of color. But yes lets play like race doesn't play apart in this... All for science.... cheerios jack.

    But everything can be come a racists story right... all about what side of the fence you are standing on.

    Posted by KJ on February 1,2010 | 01:42 AM

    Facinating and very enlightening story. It's unfortunate and very unfair that the courts have deemed that removed/discorded cells are not the individual's property, but the cells become the property of whoever removed it to use and sell to others for research. I wonder, who payed who for that court decision/finding. Does this also include sperm cells, eggs cells, and, heaven forbid, embryonic cells, removed for testing? (My, this could be another book) Please note, that prior to any operation one must sign a document acknowledging and giving authorization for testing and distruction of such tissue, in doing so you release rights to it. This is unclear to most people and usually is not a subject of concern prior to surgery, but after this book I am sure people will be more inclined to think about it more and maybe, even as a whole, think about addressing this legally in the future.

    Posted by J. Lawson on February 1,2010 | 01:43 AM

    will it cause any damage to a donor if samples were taken from his/her body? granted the scientists took her cells without her and her family's knowledge but wouldnt it be nice to know you somehow contributed in a way to science, developing vaccines for other possibly incurable diseases that will kill a whole lot others. why not go for tissue culture? why should human cells not be used for this and what are the alternatives?

    Posted by Nikki on February 1,2010 | 01:43 AM

    Truly an excellent article and I will read the book. For the last 30 years, I have known about HeLa cells and their use in science. I am glad now to know more of the story about the donor's life. Does anyone know how to petition the Nobel Committee so that Henrietta Lacks should receive a Post-humous Nobel Peace or Science award? Contact me if you do.

    Posted by Carrie A. Chism Delaney RN BSN on February 1,2010 | 01:43 AM

    Compelling and fascinating....I would personally like to learn more about the family through books, articles. The benefits from this are phenomenal to say the least. It was an African American that helped to discover or solely discovered a way to technologically communicate; what we now know as the world wide web (sorry Al Gore!). We cannot change history but we can change the way w are going forward now. Remember the atrocities suffered by so many and look at them in shame (this includes slavery, denial of respect due to skin color by ALL races) and turn what information is now at hand and utilize it to change the present into a POSITIVE tomorrow. Who cares what color this woman was/is, if reparations will follow, etc. Thank God the rest of the world can thank the daughter that her mother made such a huge contribution to medical science!

    Posted by Kim on February 1,2010 | 01:44 AM

    "A doctor at Johns Hopkins took a piece of her tumor without telling her and sent it down the hall to scientists there who had been trying to grow tissues in culture for decades without success."

    Key words: without telling her. Do you think that this would have been attempted on a white female during the time period? That seems like a loaded question to ask, but the answer is an obvious "NO!" Which brings me to my next point. Any time doctors or medical professionals take samples or do/test something on people's bodies without telling that person and getting consent, is WRONG. And to those of you who live in a "happy place" where you remain "colorblind" and say that "it's not about color it's about research," I would urge you to do some "research" of your own and look up sterilization practices on slave women, and on all sorts of brown and red women (and men) in US history or maybe the Tuskegee Syphilis study.

    Then, re-evaluate your "colorblind" argument, and come to terms with the nasty truth. Which is something that, apparently, this writer has not done... although she claims to have graduated with an upper level degree. To OVERLOOK the fact that this woman, a black woman (a POOR black woman)'s cells were taken shortly before her death and without her consent, within the context of black and brown BODIES being used as EXPERIMENTS and research without consent, definitely deserves FURTHER examination and at least recognition. Otherwise, to me, her book is worthless and does Henrietta and her family an INJUSTICE.

    If this woman were a woman who was tested on during the Holocaust, would everyone's reactions be the same? Would her being dead make it "okay" that she had samples taken without her consent, and turned into records and scientific knowledge? Please, don't lose sight of the ethics. If we lose sight of ethics, we have begun to lose sight of what it is to be human. Hopefully this author will come out of colorblind fluffyland soon.

    Posted by What?????? on February 1,2010 | 01:44 AM

    science has once again given us hope for a cure to some of these ailments.thanks Mrs.Henrietta Lack

    Posted by virginia robertson on February 1,2010 | 01:44 AM

    i find this article very interesting! AWESOME!

    Posted by jedi on February 1,2010 | 01:44 AM

    Quiet fascinating … please keep us posted! Excellent work Rebecca Skloot

    Posted by on February 1,2010 | 01:44 AM

    That is fascinating. I worked with HeLa in grad school in the 70s and I would always wondered about her.

    How do I find the book? I love to read good human interest storing and this has a scientific twist. Great.

    Posted by Monica Dawson on February 1,2010 | 01:44 AM

    This was a wonderful article! Henrietta Lack's story should be written in every history book. Everyone that figured Henrietta's family shouldn't receive some compensation, or are 'greedy', are people that most likely have enough money to live on. Try living in true poverty a couple years, then re-think your statements.

    Posted by mary kopas on February 1,2010 | 01:44 AM

    She was a mulato" woman. No black, sorry.

    Posted by claudia S on February 1,2010 | 01:45 AM

    Unbelievable, cells that never died; interesting piece. Im currently attending a community college and im sure that my proffesor will be intrigued at our next discussion.

    Posted by ptst on February 1,2010 | 01:45 AM

    Wow, what an amazing article. I Do not believe what the Doctors did was malicious. Was it unethical, definitely. Does he owe the the family an apology, of course. But let's face it, back in the 1950's almost anything could be done to a person of color without recourse.

    Posted by Marsha on February 1,2010 | 01:45 AM

    In the 70's I had hepatitus. I was in the hospital and they believed I would not live. The lab milked my veins for the virus 2- 3 times a day to make vaccines. They did not tell me what they were doing , I found out later. They cashed in on me, and I never got a penny. I am happy for those who received the benefits, but this was an exploitive kind of theft by todays standards of biology and patented genes etc. The experiments with steroid drugs made it possible for me to live although I spent an entire year bedridden.

    Posted by JRS on February 1,2010 | 01:45 AM

    this is scary to me the way the cells r still living and they don't now but I think they should of given the money to the family and ppl that work in the lab will kill things and ppl to get an answer I guess not sure but I'm scary

    Posted by Wan on February 1,2010 | 01:46 AM

    that was an interesting article... the moment i saw the topic, it caught my attention. hope to know about "HeLa" cells and the family behind it. pls update us of any new info.

    congrats to cristie jee tumulak for having passed her nursing board exam... ;)

    Posted by cj tumulak-manubag on February 1,2010 | 01:46 AM

    Why is everybody so concerned about the family being "compensated" for a sample of cancerous tissue?! I have had so many biopsies taken, little cancerous pieces of my flesh that I assume are thrown in medical waste dumps somewhere. But if someone found something useful to do with these nasty bits, something that could help others, I would be happy. And I can't imagine my sisters drumming up plans to get $$ for diseased little pieces of me.

    Posted by Teresa Bergen on February 1,2010 | 01:46 AM

    Two words for the article/book: "Master-Piece"!

    Posted by hanif tuwa on February 1,2010 | 01:46 AM

    This was an amazing story. I was hooked to it when i first saw the post. This is just incredible. I love to learn new things and this is just another fact that i did not know. I have something new to tell my kids if they ever ask me about cell research.

    Posted by Arturo Deleon Jr on February 1,2010 | 01:46 AM

    God bless America, another kick for another black family, and I bet the author will flourish and not the family who she hounded for information. $'s for the medical field and the author, America's is wonderful. Another one of their well kept secrets, but they got greedy and wanted to examine the rest of family to see what else they could they could use to help promote the medical field and keep it out of the reach of the poor. Discover great things from the poor and they can't afford to buy it.

    Posted by debs on February 1,2010 | 01:47 AM

    wow! that's nice and also made science and technology more innovative!! yet, it's kinda creepy.. LOL XP

    Posted by sheila on February 1,2010 | 01:47 AM

    As a physician and scientist and mostly a Father and human being, I am APALLED at the total lack of knowledge of the general public and the SUSPICION in which the medical community is viewed. Cancer IS NOT CONTAGIOUS, this contaminated OTHER CELL CULTURES, IT CANNOT CONTAMINATE PEOPLE!
    When this cell sample was taken NO ONE had even an INKLING that it had any scientific value, LET ALONE monetary value.
    There was no devious intent.
    A researcher simply wanted to know more about cancer and HER TISSUE SAMPLES WERE READILY AVAILABLE from her treatment. She was NOT SUBJECTED to anything other than the regular treatment of her cancer.
    It was an amazing and glorious chain of circumstances that her cancer contained a mutation as part of becoming a cancer that made it immortal (that is what cancer is! a loss of the cell cycle's control!) What an amazing thing that this woman touched the modern world in this way! I lost my father to a heart attack when I was 16, and I would take great solace if he had lived on in this way some how! Like being an organ donor to the ENTIRE WORLD!
    But she was neither wronged nor harmed in this story INTHE CONTEXT OF THE ERA IN WHICH SHE LIVED.
    This is not about race, or blood lines. It's about a victory for the human race and for a strong woman who died too young.
    This could not happen without her permission today.
    If it was not HER cell line it would have been someone else's. But WHEN?
    Her accidental contribution to medicine is ENORMOUS.
    I have personally held these cell culture lines in my hand, and not given much thought to the amazing story behind it.
    Compensation? Hardly.

    Posted by Geoffrey D Snyder on February 1,2010 | 01:47 AM

    I belive the family should be compeseted..And its an amazing story.

    Posted by philip on February 1,2010 | 01:47 AM

    We must never forget that we humans alone have the power to unlock this"Pandora's Box" that God gave us! Yet we must always be aware that our intellectual strivings must be combined with human foresight, ethics, and morality! All things that God Blessed Us With, yet we tend to devalue them, claiming them to ourselves, as being of our own genius. WRONG!

    Posted by James Ghrist on February 1,2010 | 01:47 AM

    WOW...i was really shocked to hear this in a way but i could not stop reading this article. I'm not a fan of reading but i even read the comments that people have posted. it was wrong for them not to let the family know of the HeLa cells but it had to be done. the scientists were wrong for that but they had good in mind. they have helped just as much as henrietta. i've enjoyed hearing about this story so much that i would like the book. i'd even enjoy watching the movie if they ever made one of it. thanks henrietta and may you be with good.

    Posted by arnulfo villarreal on February 1,2010 | 01:47 AM

    Great article, thanxx, What an amazing event!! , need to know more.

    Posted by Marian on February 1,2010 | 01:48 AM

    AMAZING! Im reading this ASAP! I hope the family gets what they rightfully deserve.

    Posted by tracy on February 1,2010 | 01:48 AM

    I believe that this is part of the prophetic events in the bible that man will live 1000 years once the Christ reigns. Amazing!

    Posted by Dr. Ivler on February 1,2010 | 01:48 AM

    Have you ever thought of this story being a movie it is actually very interesting for a person that does not like Science or to read i really enjoyed the article! Great Job!

    Posted by Carmen Martinez on February 1,2010 | 01:49 AM

    will it do the donor any bad to have his/her cells studied especially since for research purposes? granted her cells were taken without her and her family's knowledge but imagine how much lives could be saved because of that contribution. why not go for tissue culture? is it not good to use human cells for this? since we have millions other cells in our own bodies and have the capacity to regenerate, are there any alternatives besides human cells, animals perhaps...very interesting topic

    Posted by Nikki on February 1,2010 | 01:49 AM

    All i have to say is we are living proof that any thing is possible. Cant wait to buy the book and find out more about the her cells,this story is so interesting.

    Posted by BeBe on February 1,2010 | 01:49 AM

    thats an amazing story.

    Posted by Hans on February 1,2010 | 01:49 AM

    Wow this has really caught my interest i want to go buy the book tommorow! Great article!

    Posted by Jessica on February 1,2010 | 01:50 AM

    Wow, what a nice story. This is the ever life story that moves.. And the man that figure this out is really brave.. Keep it up, as i have learned allot from this book.. It is very good to be wise, even in the Old Testament, when Jesus was born, it was only the Wise once that went to see him... You really did it with wisdom and its all sounds interesting.. Lol.

    Posted by Jenny on February 1,2010 | 01:50 AM

    what a great contribution for science!!!but all people do u know who's d greatest scholar that actually found this 'piece' a very long time ago???find it out urself...

    Posted by haikal on February 1,2010 | 01:51 AM

    What a history, great writing and interesting story. This is the type of story we want to read. Thank you.

    Posted by Tupou Layton on February 1,2010 | 01:51 AM

    Thats a miracle story from among human compilation of science oriented causes..she must be of pure genes and heart that is why she was blessed..

    Posted by Harry Borrega on February 1,2010 | 01:52 AM

    What an interesting story, much to learn off.

    Posted by ingridbieker on February 1,2010 | 01:53 AM

    why am i not surprised about the findings of this woman. what is sad is white sceintst had been experimenting on african americans for years before civil rights from what my older relatives said . what about the men who had VD and they wanted to see how blacks react to it compared to whites and if yall do not know back in the 40's and 50's in some cities they promised free health care assistance and would sterilize black children.

    Posted by momo on February 1,2010 | 01:53 AM

    Quiet fascinating ... please keep us posted! Excellent work Rebecca Skloot.

    Posted by Mart on February 1,2010 | 01:53 AM

    thanks for the article! im a big fan of science and space but i was never taught or discovered this. im very intrigued. might look into the book.

    Posted by Professor_Goat on February 1,2010 | 01:54 AM

    What an amazing story by a very talented author, very impressive piece, I will definitely be buying the book.

    Posted by Carri on February 1,2010 | 01:55 AM

    And what work,time,energy ect. have the family put forth for this "compensation"? Why and How in the world did this become an issue of "monies"? This is a wonderful story about an amazing woman. Period! Not a racial issue, Not a money issue, just an awesome piece of History!

    Posted by Angel on February 1,2010 | 01:55 AM

    really outstending writing. the story is gripping. i as well would love to read more. as far as the family getting compensated, they should if other people are making money off of their moms cells so should they. science has come a long way now and i bet anyone if asked to donate cells for the good of meicine and research in this day and age would jump at the chance. back then most didnt know what science was doing or trying. but we have alot to thank for what has been done then and now.

    Posted by jesse on February 1,2010 | 01:56 AM

    Hope a trial Lawyer will find this article. John Hopkins should be sued and charges filed against them.

    Posted by L. Jones on February 1,2010 | 01:56 AM

    What this article fails to highlight is that cancerous cells are in fact immortal. There was nothing unusual about Mrs. Lacks cells...the article infers otherwise. Anyone with a fundamental understanding of biology would know that cancer cells continue to replicate.

    Cells afflicted with cancer (as was the case with Mrs. Lacks cells) are "immortal" due to their endless ability to replicate. Normal cells stop replicating and die after a certain number of replications. This is why most people if they live long enough succumb to cancer. Their normal cells have ceased replicating (died off) or mutated into oncogenes (cancer cells).

    Just trying to keep real here. Yes, it's an interesting story, but lets not get carried away with vampiric immortal cells. If George Hamilton succumbed to Melanoma (a likely candidate), his cells would also be pulling a Dracula (immortality) 50 years from now!

    Posted by Dracula on February 1,2010 | 01:56 AM

    I was just 17 but I got so interested about H.Lacks story. You're indeed a great writer. I love biology so much now and even when I was in high school. I am very eager to share something new in the class every discussion we make. I guess this one would be another scoop for me. It's a great piece and story.

    Posted by mapple on February 1,2010 | 01:57 AM

    This article is much misleading. The truth is all CANCER CELLS are immortal when maintained in a proper laboratory environment. If you are thinking of buying the book, please know this upfront.

    Now lets see how long it takes science to figure out how to trick the non cancerous cells to replicate endlessly. Right now there is a limit of about 70 replications for each cell.

    Posted by The Truth on February 1,2010 | 01:57 AM

    this is a very touching story in the field of science and medicine......at the same time a moving case about racism. let us learn a lesson here and let us take a moral stand over this issue.

    Posted by jocelyn macaspac on February 1,2010 | 01:58 AM

    Amazing story.Hit the stores we need this book

    Posted by Eric Mutua on February 1,2010 | 01:58 AM

    she died of cancer? HOw many people injected with her cells died of cancer also? Scientist didn't mention the side effects on the sampling of Hela. Stranger thing is that the cancer rate increased over the years, after all the injecting...creepy!

    Posted by Food for Thought on February 1,2010 | 01:58 AM

    great story!!! i want to know if the family received money? also, it wasnt fair that the scientist didnt say anything . that is the way they are going to be treated.

    Posted by esthela on February 1,2010 | 01:58 AM

    All the doctor had to do was go to Henrietta Lacks and tell her they would be examining the tissue they took from her and the research would be used to help others. See how simple that was? You know that she would have readily agreed and not even thought of compensation. It did not occur to us in those days to expect compensation for taking out a cancerous cell mass, unlike today when people want to be compensated for stubbing their toes when entering an elevator. Still, it would be nice if some lab or hospital were named after her. She did an immense thing for humankind and did not even have the pleasure of knowing she was doing it. That is sad. Through her we all have been blessed.

    Posted by Lynda on February 1,2010 | 01:58 AM

    in the end...we can say...THANK YOU GOD FOR YOUR MARVELOUS WORKS...she was an instrument..an angel sent to reveal your message!nothing encompasses when HE created MAN!

    Posted by Eppie on February 1,2010 | 01:59 AM

    I was born in '51 and I know that my mother didn't have the money to have a coat with a fur collar and my father didn't have the money to own his own suit & tie like the one in the picture of Henrietta & her husband. I guess that we was poor too and didn't know that folks owed my family for somethings that happened to my Irish great-grandparents when they were forced to come to America from Ireland - they didn't get compensated for it. They worked so very hard to become "Americans" who have an Irish background.

    Posted by Anne on February 1,2010 | 01:59 AM

    This article is much misleading. The truth is all CANCER CELLS are immortal when maintained in a proper laboratory environment. If you are thinking of buying the book, please know this upfront.

    Now lets see how long it takes science to figure out how to trick the non cancerous cells to replicate endlessly. Right now there is a limit of about 70 replications for each cell.

    Posted by The Truth on February 1,2010 | 01:59 AM

    Well, as for my brother, sister and me, we are alive today because of new experimental treatment during our childhood.
    Thanks Henrietta,

    Posted by R. Crooks on February 1,2010 | 01:59 AM

    im from clover and id heard of the HeLa cells but i didnt know it was from henrietta's. i know some of her family members. this was a great piece and its a story that should be told. thank you.

    Posted by cleanuphittr on February 1,2010 | 01:59 AM

    One of the BEST articles I have ever read!

    Posted by R on February 1,2010 | 02:00 AM

    Prior to 1962 the medical field took whatever they wanted for experiments. Unbeknown to every race, creed and color! That is why we have had consent forms since 1961 for everything when treated at a hospital or doctors office. That also includes them not responsible if you die! Her heirs deserve a substantial settlement for this harvesting of lab creations for monetary gain, and it doesn't matter what color she was!

    Posted by Kim on February 1,2010 | 02:00 AM

    Great subject....getting close to god's invention of human beings!

    Posted by Thiru on February 1,2010 | 02:00 AM

    This is very important in the name of immortality.

    Posted by mehmet on February 1,2010 | 02:01 AM

    It just goes back to that old saying,what ever is done in the dark will come to the light.

    Posted by Dorothy on February 1,2010 | 02:01 AM

    Has there been any other donors with immortal cells since HeLa? Somewhere? I find this fascinating, and would like to hear more stories dealing with biology and science.

    Posted by gleekgirl on February 1,2010 | 02:02 AM

    GOD is so wise that he created human being with immortal cells. Its up to scientists to develop it since GOD gave talent to few individuals to cure patients with dreaded disease.

    Posted by Rigor Ocampo on February 1,2010 | 02:02 AM

    SPEECHLESS, Now that's a story. Well it was GOD's will that the scientist would steal this GOD's gift to earth lady's cells to help the human race out with our health.

    Posted by brand on February 1,2010 | 02:03 AM

    Great work Zielinski!! Congratulations for sure!! I will have tu hunt for this book and buy it!! The word of God assures us of prosperity! Indeed Sarah let this family get involved, I know that the amount of money lingering in the pockets of those scientists can get a descendant abilities of becoming a renown great scientist in this world!!

    Every one concerned lets join hands!!

    Posted by Linnah on February 1,2010 | 02:03 AM

    Sounds like the path to immortality for researchers.
    I hope her children will be cared for via a 'monetary trust' since the world has used and still needs the use of her immortal cells. They have a right to her legacy as an inheritence, which the world has been utilizing as a means to save others.

    Posted by L Ably on February 1,2010 | 02:03 AM

    This is very interesting, like everybody else I feel the family of this woman should be compensated and also that doctors and scientist alike should seek the consent of the persons or people involved before proceeding in other to enhance Human dignity. However the most important lesson of all is that under perfect conditions Humans can "Live for Ever" since we are made up of billions of cells.

    Good Job on the article.

    Thanks.

    Ola.

    Posted by ola on February 1,2010 | 02:04 AM

    I believe that the fact that so much benefit has derived from the cellular line developed and propgated by scientists brings up a very significant issue. Who really has the rights to her cellular line? I am sure vast profit has been generated from a sample she was never made aware of, how many other people have bits of themselves traded n a marketplace that the "donor" is never made aware of? Doesn't her family and heirs own the rights in part at least to the benefits generated from her serepticious removal of her cells, no matter how benevolent the intent. How many of us have our cellular selves generating a profit for some pharmaceutical company without recognition or compensation for the informed or uninformed "donor" or more appropriately vitim of theft. I feel this woman's heirs deserve to be greatly compensasted, as should the many other "donors" who remain unknown and unnamed!!!

    Posted by Gerald Gilliam on February 1,2010 | 02:04 AM

    I don't think that the medical industry should be able to own biological property for the purpose of making obscene profits that bankrupt the patients. Making billions of dollars way beyond the cost of research, developement, employee compensation, resource procurement, corporate risk and shareholder contribution is what I mean. I know that it can cost a lot of money to develop a product. There should be compensation. At the same time, don't treat a human being as if we somehow don't deserve compensation when you want to make money off of that person.
    People are not lab rats or some weed in a field to be used with no second thought. This capitalistic system has set the rules when they expanded ownership of intellectual property to that of biological tissue. Why is this poor family being castigated as greedy for wanting compensation after their mother's valuable contribution to humanity? They should have at least some right to biological ownership. When the medical industry can make trillions from a person's cells, that person and their immediate family should be richly compensated. We are not lab rats and should not be treated as such.
    If something unique about your body could be used to cure many diseases and you stipulate that no medical industry could monetarily profit by bankrupting patients, what do you think would happen? I wonder if that doctor ever tried to cure Henrietta Lacks, or did he just send her home like those so used in the Tuskeege "experiment". Lab rats indeed.

    Posted by Marge on February 1,2010 | 02:05 AM

    Fascinating HeLa cells. WOWWWWWWWW. Thats incredible to learn.

    Posted by Susan Karungi Loise on February 1,2010 | 02:05 AM

    I disagree with the gentleman who wrote that Henrietta's family must have a "welfare mentality" because they want some kind of compensation for her stolen cancer cells. Many people receive financial compensation for their participation in medical research studies. I am a scleroderma (an autoimmune disorder) patient. In the 1990's, I participated in a patient study. The researcher took a tissue sample from my arm, and closed the wound with a few stitches. Yes, I received a small amount of money for my participation. However, I would have participated for free, and I consider the scar a "badge of honor". I look at it with pride, because I was helping other patients like myself.

    I don't know if Henrietta's family would be eligible for compensation, but merely asking for it does not mean they have a "welfare mentality". At least nowadays, compensating people for their participation in research is commonplace.

    Posted by Tomisa Starr on February 1,2010 | 02:06 AM

    I believe the heirs of Henrietta are entitled to the profits derived from the use and sale of the Hela cells. The cells, being a necessary part of her body, are personal properties of Ms. Lack. They were extracted from her without her knowledge and consent which made the extraction and possession by third parties of the said cells illegal. The immortalized Hela cells are deemed stolen goods and those who use, sell and profit from them are deemed to be accessories to the crime of robbery. As such, all money derived from the illegal sale and use of the hela cells, specially now that the incident has become of public knowledge, must, and should belong to Ms. Lack's heirs. They deserve every cent of it. I advise her heirs to secure the services of a good lawyer to protect their interests.

    Posted by Godfrey on February 1,2010 | 02:06 AM

    Does Oprah know yet?

    Posted by Mom on February 1,2010 | 02:06 AM

    everyone who has had any cancer screening or blood draw should look into this case as it was stated in the article that her cells were taken and used for research without her knowledge. Cancer screening and blood draws benefit patients but who knows if they really discard after what they do what they say they're gonna do.

    Posted by Jayne on February 1,2010 | 02:06 AM

    interesting..

    Posted by cherry on February 1,2010 | 02:06 AM

    I find it to be hugely ironic though. . . . .Every level of capitalistic institution of the medical industry was able to make trillions of dollars from the uniqueness of this woman's very birth. On the other hand, her family is so poor that they can't pay for any of the cures that were discovered from Henrietta Lack's cells if they needed the care. To those who wish to diminish Henrietta Lack to something less than human, she has probably saved lives that you cherish, simply by being born. So far, no one else on this huge planet can make that claim. . . . . .. . .

    Posted by Marge on February 1,2010 | 02:07 AM

    This is mind blowing!

    Posted by Laketia on February 1,2010 | 02:08 AM

    first of all i would like to thank all the survivors of henrietta's family members. she is like an elephant, because after the death also we use some parts of the elephant know. she is like a match stick or candle because they end their lives after giving lights to us.

    Posted by sm.balasubramanian on February 1,2010 | 02:08 AM

    amazing story, the family of Henrietta should be compensated, i agree with one of the comments, taking someones cell without her knowledge is like robbing someones property and i think its a criminal act, a robbery in broad daylight..other people earned a lot of money over someones cells is I think, unfair..

    Posted by John A. on February 1,2010 | 02:09 AM

    Why so many comments about compensation to the family? If I were told that my cells could save the lives of millions if not billions of people and change the course of medicine as we know it; all from a discarded cancerous tissue sample, would that not be payment enough? And if the doctor were truly a racist, he would have never contemplated trying to replicate a black woman's cells as the key to unlocking this miracle. This is such a great story and it is saddening that race and monetary value has to be associated with it.

    Posted by Heather on February 1,2010 | 02:09 AM

    Glory be to God. The bodies of prophets do not decompose. Nor do the bodies of righteous people who believe in God. This is according to a saying of Prophet Muhammad, peace be upon him -- God's Final Prophet to All of Humanity.

    In Illinois, there is a lady from the 1930s whose body is not decomposing and she is on display in a small museum in a small town. I forgot the name. You find examples of this all over the world.

    Posted by alexander on February 1,2010 | 02:10 AM

    I can't imagine her type of cells being unique. Instead, I can imagine them being extremely rare.My forfetched conclusion would be that at some point in history all human beings entire bodies were immortal. The highly abused soil of today is far too weak to produce extra-super-duper fruits and vegetables capable of enabling human beings to become immortal, as it once did. The few immortal cells remaining upon this planets, like Harriet's, are ancient survivors. They are the most valuable endangered specie of them all.

    Posted by samuel mims on February 1,2010 | 02:10 AM

    I see a lot on here about compensation, and cries of theft. And I'd like to say, wow, really? Sure, now that they know about what her cells are, and what they've done, compensation would be good, but at the time, how could the doctor have known about the worth they would have in the future? And theft? That's incredible that you're indignant about the doctor "stealing" those cells. Personally, I don't mind contributing to the human race as a whole, though I doubt that I have anything special that would be as useful as the HeLa cells, and if I found out that my doctors took something from me that didn't hurt me in any way, and it helped develop new medicines to save lives, I'd probably kiss them.

    Posted by Ipo on February 1,2010 | 02:10 AM

    Amazing article! I've worked with HeLa cells in my research, so I knew a little about where they came from, and of course what HeLa cells are. It was amazing to learn a little more history of Henrietta Lack. Thank you! I look forward to reading Ms. Skloot's book!

    Posted by Don on February 1,2010 | 02:11 AM

    It is really sad the way this story plays out. I am glad for the advancement of modern medicine, but the way credit was given to Mrs. Lack was a little disrespectful in my eye. Mabye I am wrong, but I am tired of reading about the lack of education, and how poor black people were durig the times of slavery. Was it really necessary to exploit the family? If you dont know what I mean, I am talking about how the brother was homeless, and how no one cared until money waws involved. Myself, like many Americans know that the family of Mrs. Lack will not be compensated for her cells, but atleast let the world know of the great discovery of living cells without the discrace. Thats like me saying Elvis Presley died a great man, but before he died, man he was FAT and STINK. Its just wrong no matter how you look at it. If you have a comment to direct to me, hit me up at aguas26@yahoo.com

    Posted by J Wat on February 1,2010 | 02:11 AM

    How quickly this fascinating HUMAN story became one of race and exploitation. Sharpton, Jackson and all the other racist ambulance chasers are a little late in jumping on this bandwagon. Give it up and be proud that your relative was a silent, unsung medical hero. There are countless people from all races and walks of life out there who don't expect "compensation" for what they wittingly or unwittingly have contributed to society. I'd say the real shame in this story is on those seeking a free financial joy ride from something they never had a thing to do with. My great grandfather died in the Ellis Island infirmary from neglect, yet our family who did live and work like slaves in the sweat shops of NYC never sued the federal government for compensation, in spite of the impact it had on our family. Financial joy-riders tarnish Mrs. Lack's memory. This is a story about honoring a medical heroine, not financial gain.

    Posted by D.C. Tuncay on February 1,2010 | 02:12 AM

    I'm a biotech student and I've worked with HeLa cells before. I've tried asking my lecturer what HeLa stands for but he couldn't give a straight answer. This is a great explanation! ^^

    Posted by Sofie on February 1,2010 | 02:13 AM

    The priviledged sector of any society will never realize the long term effects of discrimination the less valued class endures. This story is a great historical fact that once again shines light on the contributions of Blacks to our society. Yes, times were different and things were done differently, but the fact remains that Blacks were treated with less than their value as a people. It's typical for someone to say that the family does not deserve any form of finacial compensation, but to what end has this woman's DNA changed the face of medical discovery? Who is to say that the use of her DNA is not on the same par as any major medical dicosvery of this century? While it is true that the discoveries in this case were stumbled upon by White doctors, it is no less deserving a contribution as the recognition so many other less significant things receive. Why is it so hard to give credit where credit is due? A black woman's cells have helped to save thousand, maybe millions of lives of all colors. I think with all the money made in the medical field, this family should be shown some compensation for their mother's contribution. It's like using/stealing the best part of someone else's Doctorial thesis to get your PHD and not listing them in your bibliography. WRONG, simply.

    Illya A. Sowell (Black American)

    Posted by Illya A. Sowell on February 1,2010 | 02:13 AM

    Just came across this article. It makes extraordinary reading. Yes,there was bound to be the inevitable cry of exploitation and racial shenanigans, however, without exploratory endeavours of our erstwhile scientists,white or black; the advances witnessed today would have been non-existent. Kudos to the author of this revelatory book. It will make a difference. The family invloved are entitled to rewards...good karma must follow.

    Posted by Obi on February 1,2010 | 02:13 AM

    I think this is a great contribution to science. Enough of the welfare addicts more worried if they can sit back and get a check off somebody than being happy or proud that a great contribution to science has been made that is benefiting millions, and probably themselves more than money could do. How selfish. Shame on you guys looking for a quick buck.

    Posted by Dan Wiedell on February 1,2010 | 02:13 AM

    the family will probably get compensated by the book sales.

    Posted by stephanie on February 1,2010 | 02:14 AM

    this article makes me want to buy this book and as a young reader I hope the HeLa cells may contribute to good use and that the company may help Lank's family out of poverty or at least pay them(cash) for the use of H.Lank's cells.I hope Henrietta is with God now watching over Deborah and her brothers. :P

    Posted by Josh on February 1,2010 | 02:14 AM

    Amazing! Great writer who leaves the most intriguing part for us to purchase the book. How can I get the book in Kenya?

    Posted by Mu on February 1,2010 | 02:14 AM

    Great read and great information!

    Posted by CK on February 1,2010 | 02:15 AM

    All cancer cells are "immortal". There is nothing new in this article except an attempt to grandise a simple procedure(by today's standards) into something greater than it is.

    Posted by Rodney Harris on February 1,2010 | 02:15 AM

    One should not take it as easy. It is a crime committed by a white scientist using some one's body parts ( whether it is black or white ). Any how, if the actual lady could not benefited at least her kids should be.

    Posted by Kaifi MM on February 1,2010 | 02:16 AM

    I too found this article to be most educational, amazing, and fasinating. The thought of cells continuing to live this long past the individuals death is truly a miracle, one that only God could have blessed. The scientist in this article obviously saw something in this womans tissue sample that they found interesting, because I know that she was not the first woman to come to them with cervical cancer. There had to be something special that they witnessed for them to go to those underhanded measures to steal a sample without her permission. The article stated that her husband only had a 3rd grade education and did not understand what had happened to his wife, which tells us that this family was and continues to be taken advantage of. This womans cells were essential in deveoping the "Polio Vaccine" and "Gene Mapping" "Vito Fertilization" and even sent up into space to see what they're reaction to "Zero Gravity" would be and we don't even know how many million of dollars in grants have been given out just from the many developements that have already come from these immortal cells. I believe that her name was not changed or kept a secret to protect the family, but to protect the scientist who stole the cells in the first place from the family eventuallly wanting their share in the monatary windfall.

    Posted by mssweetella on February 1,2010 | 02:16 AM

    I was also thinking about that doctor at John Hopkin's that removed the first tissue, was he treating Mrs. Lack? How did a black woman during that time period get "treated" at such a prestigious white hospital? Could it be that since they had been trying to grow cells in a culture for years and failed, they "used her body to grow cancer cells" also without her knowledge. Possibly they used her and other poor, uneducated blacks in the place of cultures. Maybe she never had cancer prior to the cells being injected into her to use for experiment. What happened to her after the tissue extraction, did they treat her for the cancer? That was not mentioned, however since she died at 30, we can assume she wasn't treated. This type of known history is the reason so many black people are suspicious of being involved in research projects or checking donor on drivers license.

    Posted by J. Lawson on February 1,2010 | 02:16 AM

    very nice..i will find that book and buy it

    Posted by escarlet on February 1,2010 | 02:16 AM

    a very interesting story and as a white person it has no bearing on color that the story made me want to go buy the book and get more information concerning the family and circumstances involved with tissue taken without the persons knowledge of the use of their own cells.

    Posted by dave nelson on February 1,2010 | 02:17 AM

    Omg ! sounds very interesting , i would love to read the book. This is an encouragement,to study more in the field of science .

    Posted by aisha on February 1,2010 | 02:18 AM

    I just hope things are discovered in uour lifetime so that we can become immortal and escape the lonely planet of death!

    Posted by Imrez Chowdhury on February 1,2010 | 02:18 AM

    A wonderful true story.

    Posted by Rahul Kaushik on February 1,2010 | 02:19 AM

    How did they use cancer cells to make a polio vaccine?
    How do they kill the cancer cells before the vaccine is given to Babies? What? I know research is expensive, I understand that, How can this be safe?

    Posted by Kat on February 1,2010 | 02:19 AM

    Aren't cancer cells meant to divide rapidly? I guess that's what kept them alive. A slamming article.

    Posted by Layla Saad on February 1,2010 | 02:20 AM

    A nice one there. Maybe this story will bring her family to the limelight and they can be compensated.

    Posted by Lenny on February 1,2010 | 02:20 AM

    The story and the scientific evidence is just confirming that Human soul is really immortal.

    Henrietta lives on somewhere in eternity. Where would you spend your? In heaven? or ...

    Posted by Akindele on February 1,2010 | 02:20 AM

    now u have just made me interested in cells very amazing story but what does it all mean can we clone people can we make people live forever i mean sometimes people need to get educated on this stuff

    Posted by curtiss on February 1,2010 | 02:20 AM

    wow, i thought HeLa cell was an abbreviation for a certain scientist... as a biologist, i never knew that HeLa cells came from a cancer patient

    Posted by antolyn exconde jr. on February 1,2010 | 02:20 AM

    I'm interested in this story.where can I get the book?in Malaysia?MPH?

    Posted by emmanuel on February 1,2010 | 02:20 AM

    Whew! watta intersting info! :)

    Posted by khye vista on February 1,2010 | 02:21 AM

    Talk about "tell me a story"! HeLa, la, la, la! What an umbrella she has created.

    Posted by Kawaiopua on February 1,2010 | 02:21 AM

    It is good to ask the right question after the dust has settled? Of the many questions that come to my mind, one that I feel requires further reflection is:

    What made Henrietta's cell immortal?

    There are many other reflective questions but these could be raised at a later date.

    Posted by Jagjit Singh on February 1,2010 | 02:21 AM

    I find it interesting that donner cells are now taken anonymously. The fact that ones DNA may contain a cure and one may never be compensated for that is only the tip of the iceberg. If noone knows whose cells are presenting a unique health or life threatning strain noone will know how to contact the subject to help them and their family. In medical journals patient images are included more often than not. Do they supply concent to this? What are patient rights if they would rather their images are not presented in case study?

    Posted by Star Z on February 1,2010 | 02:22 AM

    It's amazing how many people are interested in reading a book about a supposed "immortal cell". How can anyone be certain that the cells are going to live forever? After all, it's been less then 60 years since the cells were harvested. There are individuals all around the earth who live beyond the century mark. Immortal implies forever. Have you ever pondered "forever" ? Is living a thousand years forever ? or perhaps a million or even a billion years ? What percentage of forever would even a thousand trillion years be ? 50%?, 25?%, 1%? That huge number with enough zeros behind it to atretch to the most distant galaxy wouldn't even be negligable compared to forever. It's an infinate number and our finate minds cannot comprehend infinate. Again I say it's amazing that so many people want to read about the "immortal cell" when there is a book that comes with a 100% guarantee for everlasting life. Yes, living forever without any of the physical, mental or emotional problems we as humans struggle with in our everyday lives. Yet very few people want to read it and get the true sense of it that they might gain this everlasting life free of all the sorrow, pain and hardships that we all as human beings suffer through. Oh yes, I know many of you know all about it, many of you even call yourselves believers and even followers of the instructions contained within the pages of that book. But if that were the case then one of it's main characters would not have been able to say that "few find it". Even though it's the most published book in the history of our planet and it's printed in just about every language on this planet, it's true sense remains hidden or "veiled" to the people of the world. Although EVERY WORD that it's author has had written down for a witness to us has come true, we as humans still don't get the true sense of it's message.

    Posted by Zeny on February 1,2010 | 02:22 AM

    something special behind medicine and scince...
    The Hela cells important to human being like scientists..
    But..we should think about Henrietta Lacks' family..
    they deserve get money...

    Posted by mimosapudica on February 1,2010 | 02:23 AM

    This is so very interesting.I'm amazed at the fact that the writer has actually done a lot of research work which has eventually helped Henrietta's family demand compensation...which they otherwise would not have even known, they deserved. Well done Ms.Skloot !!

    Posted by Zainab on February 1,2010 | 02:24 AM

    I think it is great but but there is still an issue of consent. At any time that tissue/cells/whatever is taken from an idividuals body there should be consent before it is used for anything else. What if there is a religious issue or a spiritual issue or any personal issue at all? If her cells are still alive can she really move on to the next realm if there is one?? Cells are the basis of our lives. Once again a person , whose identity was thought to not matter, was used in the name of science without their consent. It is not right. For every person who does not want to be used in this way there are many more individuals who would want to be used.

    Posted by ruth on February 1,2010 | 02:24 AM

    its amazing .......nice story

    Posted by atar hijazi on February 1,2010 | 02:24 AM

    The h's family deserve a pay for this,did they get compensated?

    i like the story.

    Posted by Betty on February 1,2010 | 02:26 AM

    WOW!!!!!
    WHAT A GREAT STORY, I AM NOW INTERESTED IN HUMANS LIFE, AND I MORE NOW THINKING IF HOW LIFE WAS IF OUR CELLS ARE ALIVE IN MANY YEARS.

    Posted by melros on February 1,2010 | 02:26 AM

    MY THOUGHTS: BEAUTIFUL, SAD AND AMAZING, ALL IN THE SAME SENTENCE.

    Posted by KALKISWAHR on February 1,2010 | 02:26 AM

    I'm a medical genetics MSc student, but i did know nothing about the origin of HeLa cells before reading this piece. it is great that now we can thank Henrietta Lack's soul heartily. I hope that enough attention and regard would be sent to any one being helpful to the stream of science.

    Posted by D K on February 1,2010 | 02:27 AM

    I need to buy this book.. its breathtaking...

    Posted by celine on February 1,2010 | 02:27 AM

    Henrietta's cells were 'Immortal' because they were taken from her tumor. That's what makes cancer what it is. Cancerous cells begin to grow uncontrollably and if unchecked, they invade the organs of the body and become more numerous than normal human cells. Scientists, however, have learned to do research using these "bad" cells to help make more "good" cells that are needed. This research has had it's successes and failures, but that's what research is all about!

    I think one of the most amazing parts of this story is the identity of the woman & how it was kept underwraps for so long!

    Posted by Astride on February 1,2010 | 02:27 AM

    I think it is great but but there is still an issue of consent. At any time that tissue/cells/whatever is taken from an idividuals body there should be consent before it is used for anything else. What if there is a religious issue or a spiritual issue or any personal issue at all? If her cells are still alive can she really move on to the next realm if there is one?? Cells are the basis of our lives. Once again a person , whose identity was thought to not matter, was used in the name of science without their consent. It is not right. For every person who does not want to be used in this way there are many more individuals who would want to be used.

    Posted by ruth on February 1,2010 | 02:28 AM

    very interesting story. i am getting the book so i could find out more. if helacells helped with the polio vaccine then it has helped me.great article.

    Posted by andrea on February 1,2010 | 02:29 AM

    we are all a mutation of something. maybe something good or something bad/ (depending on your thaughts) all aside what she is doning after she is gone is a good thing. if she were still alive would she tell them to stop? dont take this wrong but she is gone.. her cells do not make her here. one cell or a millon+ does not make us who we are. some of us are good some of us are bad. DNA from one cell can make identical but not infanet identical. identical twins will not always eat or think like the other. to answer one question to the daughter not from one cell you cannot tell what her favoret color was. but i can tell you that her cells have made a huge inmpact on the world. i belive she was a good person and would help anyone she could. but at the same time i also belive the family should also be compansated for HER!!!!!!!!!!!!! no good dead goes undone!!!!!!!!! midical world make it right, you get paid (dont you), and you paid for the cells (company) didnt they? what has she or her family gotten??????? her sole and body may be gone, but she still helps you.. now its your (company and Dr's) turn to help her help her family. dont you think that is fare????????????

    Posted by bill norby on February 1,2010 | 02:30 AM

    hey it's nonsense find some thing more there r so many things r hidden so dont wana share ????

    Posted by mohsin ali on February 1,2010 | 02:30 AM

    woman's immortal cells changed medicine.

    Posted by kourosh on February 1,2010 | 02:31 AM

    It seems that, besides the renowned scientists that push science forward, there are many unknown others, who contribute to its progress. Long live the cells!

    Posted by Serbi on February 1,2010 | 02:31 AM

    After being exploited by scientist in the past... Now, I'm afraid, HeLa family is being exploited by the writer...

    In the past, HeLa died in poverty, meanwhile the scientists and corporates made a lot of fortunes and lived wealthy...
    Today, HeLa family lives in poverty, meanwhile the book writer booked a lot of money from royalty...

    Posted by Truelooser on February 1,2010 | 02:32 AM

    very interesting story that i read in my whole life that after 59 yrs. cells still alive...it's amazing....

    Posted by filoteo arnell on February 1,2010 | 02:33 AM

    Its one of the strangest thing i have heard ever, but now it makes me more keen n intrested in Tissue Culture...Hmmmmm i think i need to do a bit of a research as well on this n learn more about tissue culture...

    Posted by Afsa Ashraf on February 1,2010 | 02:34 AM

    Politically correct linguistic gymnastics:
    She was not a "poor farmer." If she herself was the farmer (not her father or husband) then that would have meant she was well off enough to hire men to work her farm in which case she was not "poor." She does look rather prosperous in the picture, but I think you meant to say a "poor farmer's wife." She was married by 30, at last give her that dignity instead of your anachronistic nonsense.

    Posted by Dr. Kenneth C. Dawkins on February 1,2010 | 02:34 AM

    I truly believe this Woman should recieve the title of "SAINT". Through her Cells so much has been done and so much continues to be done.
    I hope someone who works in that area will see this and bring it to the decision makers on who gets into Sainthood?

    Posted by Terri J on February 1,2010 | 02:34 AM

    It's amazing...it's like having a neverending life.

    Posted by Kinga on February 1,2010 | 02:35 AM

    hmmm.. wow..the cell actually grown or expand.. whatever, and is never out of stock???? i just don't get..anyway, she is an angel..

    Posted by vivien on February 1,2010 | 02:35 AM

    Thanks for the good article, and for all who gave their thoughts, training and foresight to use cells that Henreitta had removed from her body, and to her for what she has given to science - she was under medical care to rid heself of cancer. I hope that her family will find peace in this history of their relative, and if there is money made because of her donation I hope the family can share,I also hope that it will pay for some of the research has been done and continues. If any piece of my ailling body can be useful to the medical profession in some way that helps others = GOOD!

    Posted by Madoline McNamara on February 1,2010 | 02:35 AM

    wow! i cant wait for the movie version

    Posted by james kariuki on February 1,2010 | 02:36 AM

    Very intresting peice.
    My only problem is that the researchers could of atleast give some credit to the Lacks family--to me it looks like the young lady's cells forever changed cell reaserch and made one particular company BILLIONS almost overnight...

    Posted by Evant on February 1,2010 | 02:37 AM

    Thank you for the info///

    of course a Black womans cells could never die...well you know were she came from and were the first people came from.. So Thanks for Black History Month. or people would never know any thing about Black people/

    Posted by Monistar on February 1,2010 | 02:37 AM

    very interesting indeed!!! i would love to have a copy of this book.

    Posted by LormaFLor on February 1,2010 | 02:37 AM

    I SALUTE "Hela". This is a story of a guardian Angle who has lived on n lives on to save the world/humanity from self distraction n peace. I suggest that we set a day to honor this Great woman. On Mothers day Perhaps !!!! .TO the family, Please patner with a movie company for a seasoned classicc....

    Posted by Kimeta on February 1,2010 | 02:37 AM

    Very interesting. I would love to read he book. Big Ups to HeLa for contributing so much into the world of research and development. Her family should be proud and compensated.

    Posted by Olivia Skweit on February 1,2010 | 02:38 AM

    I thank Henrietta for the living cells as she has bruoght cures for everyone that have lived after her death and in her resting place she stills helps the living through her living cells.
    To the family i salute you and your mother.To the doctors who took the Cells without consent i feel there is a lot more to tell than what they took from her.There is a lot more that they gave her that maybe should not have been issued to her with their trials.
    I believe there is a case for them to get something back from this as they have been poor from beginning as from the time their mother was a tobbacco farmer and upto now.Maybe the reason why the cells have not died is because she will only rest after the family is well compensated.

    Posted by Lloyd Murape on February 1,2010 | 02:38 AM

    those scientists should be taken to court,this is a really sad story,but however interesting.people exploiting their neighbours,the family of H.Lack should be settled(all entitlements right from 1951).I see it as the greatest act of wickedness,this is even worst than slave trade,if you ask me,using the families ignorance against them and shying away from settling them.wickedness!!!!!!

    Posted by ivon on February 1,2010 | 02:38 AM

    it'a a fascinating and a very sad story of a woman...it all happens because of some racists in the world....

    Posted by rain on February 1,2010 | 02:38 AM

    history is made i am happy and proud to be a black african.
    had like to read the book and how much was given to the family

    Posted by adebayo elizabeth south africa on February 1,2010 | 02:40 AM

    Doctors save lots of lives; at the same time Doctors do some unethical acts. Twenty years ago my mother went for her check up, the Doctor said that her heart had to be removed or she will die in less than a year. My mother was smart enough to feel that her heart was working perfectly well. She never went back to see the Doctor. She is now 84 years old. Doctors are saying today that my mother has a baby's heart. They just can't believe an old woman has such a healthy heart at that age. I am not surprise about the story at all, my family has been there.

    Posted by Robert M. St Fleur on February 1,2010 | 02:41 AM

    This is a wonderfully written article. I definitely want to know more! As for the compensation...I don't believe these cells can really be considered as 'taken' without her permission. If she went in to the hospital for diagnosis and treatment, she 'consented' to anything done as part of her diagnosis and treatment, such as removal of all or part of the tumor. If the scientists kept a little of it for research, I doubt that was 'stealing' the poor black woman's cells. Now, that the book is out, she will be immortalized for her contributions. I wish my mother, who also died of cervical cancer had had this opportunity. She would have been so happy to have helped.

    Posted by Christine on February 1,2010 | 02:44 AM

    It is finally being shown that black people "are not" the physical weaklings that medical science likes to publish and protrait them to be. This woman cells and she had cancer, shows that all these negative reports we have been bombarded with in this country, forever that black people : have more heart attacks, have higher blood pressure, more diabetes, more strokes, are fatter, are more prone to aids, the list goes on and on than whites is nothing but fabrication. I've always believe that was the case and this woman cells are telling the world the truth. If she having had cancer and her cells are benefitting research today, there are properties in her cells that scientific research has shown, is beneficial in a major way or they would not be using them for all of these years. Thats the thing about this story, we better not lose sight of. Its like the tobacco companies know there are ingredients in cigarettes that keep people smoking, you see what I am saying. I applaud the author, for bringing this story to the forefront. Just think, at one time, all black people were good for, was picking cotton, working in the fields, remedial jobs. Now, the cells - dna, are helping people to live longer, who would have thought?

    Posted by Eric Wallace on February 1,2010 | 02:44 AM

    White or black, rich or poor.........I could care less. If the doctor initially would have asked her she undoubtedly would have said yes. If he would have offered her a paltry sum of money she would have taken it. The fact is the doctor got lucky and her cells lived when others did not. Who cares about the rest. Its just another thing for people to act self righteous and indignent over race issues. Much ado about issues all ready being beaten to death every day. Instead celebrate the medical advancements. I am sure she is not the only one in the world with these cells. Puh lease.

    Posted by Happy on February 1,2010 | 02:45 AM

    Very interesting and fascinating. This is truly stands out as one of the great and unsung contributions of a black person to mankind.

    Posted by Gideon Genesis Nyirongo on February 1,2010 | 02:46 AM

    This is really amazing.I love to know how come they live all these years!are there any other cells lived that long? could that mean there would be an immortal man on earth one day?

    Posted by Riyadh on February 1,2010 | 02:47 AM

    I am very glad that the author pursued the story and brought it to light. Everything in America is about economic status and race! If the scientist didn't think that there was any wrong doing, why keep the the HeLa's identity a secret? Why didn't the scientist obtain permission to disseminate Ms. Lack's cancerous cells? Would the doctor's have obtained permission if she had been rich and white? Why didn't the doctors, scientist, or corporations compensate the family? It also appears that there is no thought and no consciousness about all the money that corporations and scientists have made; and no formal credit with all of the medical breakthroughs that have happened as a result of Ms. Lack's cells. I hope that the scientific community will write Ms. Henrietta Lacks in the history, biology,business,law and medical books, and obtain for her the highest award that a citizen can receive in the service of one's country (posthumously). She should have a foundation established in her name by the Corporations who made so much money. Her husband, her children and grandchildren should get a formal apology from the scientific community; and some compensation,an educational trust fund, and lifetime health care for all of her generations to come as well as an opportunity to share in the author's proceeds.

    Posted by Janice on February 1,2010 | 02:47 AM

    Many of things happened in 1851 and prior years befor that. During reserch of my family and its medical history i remember reading a story about my great uncle and how he joined the circus at age 11 and wondered why should a child of that age need to do this but as i research forther i realized that we as the people had no rights over our own, and if we did we were not to know about it. and now in modern culture we think we know a lot but is still keep in the dark the less we know the better for those who governers over us for personal gain. at this point in our live's knowing is power.

    Posted by Nardal Stroud on February 1,2010 | 02:48 AM

    wow wow wow... a narrative story fill with facts, not too sure and lots of money issues...

    Posted by david on February 1,2010 | 02:48 AM

    Bravo!!!

    Posted by Paulene Ann Salada on February 1,2010 | 02:50 AM

    I thought this was a wonderful story and a clever piece to bring out for Black History Month, not something I have any particular interest in. I felt a little disheartened when I read about money coming in to it. Why weren't the family just grateful that she had lived on and helped so many after her death? But, and here is where the author is very good at her job, then I read on to hear about their impoverished lives. It seem unfair that they should be leading lives like that after all she has unwittingly done. However, I don't believe the scientists owe the family billions of dollars. It would be nice to see the family be able to afford to live comfortably, in homes and to have health insurance etc though. It is something to think about.

    What an amazing woman. I'm sure she would be most proud of what her cells have done for humankind.

    I thought the author wrote the piece beautifully.

    Posted by MC on February 1,2010 | 02:51 AM

    GOOD JOB, DIGG ON THERE IS NOTHING DONE IN THE DARK THAT WONT COME TO THE LIGHT.

    Posted by ANGELITA WS on February 1,2010 | 02:51 AM

    Why is any of this not surprising? Has anyone heard of the Tuskegee Syphillis trials of the 1930s? It's part of a historical trend of scientists and doctors knowingly using the community to advance scientific knowledge. And yes, while it's great that we can all contribute something and make great strides in understanding complicated diseases- to anybody who says it's not about race- wake up and smell the coffee. Blacks historically (from the times of slavery) have often been targeted unbeknownst to them- yet without any of the glory or compensation specifically because they were easy targets, often under-educated who wouldn't complain or present any obstacles in the reasearch or gain directly from the spoils of the findings. Henrietta L. and her family being a case in point. It's an insiduous form of racism that is pervasive. But- vive la scientific research and advancement and congrats to Henrietta Lacks for her contribution!

    Posted by vanessa on February 1,2010 | 02:52 AM

    Wow... All these views... Hmmmm..

    Some black dude thinking, great injustice was done because she was black
    Some white dude thinking, I better adopt a black child so I can undo some injustice
    Some black researcher dude thinking, I better not slip my tongue
    Some white "not so smart" dude thinking, Geez... my folks did all this research to help all humanity
    Some yellow, brown and not so-white dudes thinking, where do I fit in all this mess..
    Some non-American dude thinking, heck with these Americans, they rob every one...

    Not all republicans are rich and not all democrats are poor...

    Research does not happen just in USA. It happens everywhere and cells of every race are used in research and people from all races do research..

    Each and everyone of us benefit from this research.. You don't have to be white to benefit from all the research that goes on in this world or for that matter in USA..

    Some of us (Black, white, yellow, brown and not-so-white) give our samples for research and advancement of humanity knowingly and some of do it unknowingly...

    Some of us give blood, organs, money, caring and love and some of us have a need to take the help some times...

    It is just like most of us (White, Black, not-so-white, brown and yellow) that voted for a Black President and are proud of making the history in our life time..

    I am just thankful that one of my fellow Americans gave her cells and another did that research

    I, for one, am in debt to both for their contributions to humanity..

    God bless them.. God bless America.. God bless our President.. and God bless you.. Yah.. YOU!!

    Posted by Illias on February 1,2010 | 02:56 AM

    Ethical considerations evolve over time. As a Stage IV appendix/colon cancer survivor, I feel that my survival and recovery were due in large part to my participation in a clinical trial. One of the conditions for participation was to release all right to any biological samples taken during the course of my treatment. The accumulation and comparison of DNA profiles to treatments/results may very well lead to improved prospects for future cancer patients. I was impressed by the time and effort taken by my oncologist to discuss how my participation in the trial might help future patients. At no time, did my oncologist offer a promise of a cure due to my involvement in the clinical trial. At the start of my treatment, I was told that the best I could hope for was to have to disease become chronic rather than acute with continuous chemo (FOLFOX + Avastin) or other standard chemo for the rest of my life (a cycle 8 treatments followed by a chemo vacation over and over). He also mentioned that the very small tumors that remained after 5 hours of cancer surgery would be with me for life. My oncologist was somewhat dumbfounded that after 7 treatments, I had a no detect CT scan which was followed up by a PET scan and two subsequent CT scans that were also no detect. I was asked and did extend the number of chemo treatments to 12. To make a long story short, I was taken off the clinical trial on treatment number 12 because I “did not have cancer.” I am taking Avastin as a precautionary measure. He was rather surprized

    Posted by Charles Carrell on February 1,2010 | 02:57 AM

    Reparation for the Lacks family? Not in the least. Compensate them for the use of the family name (why did the scientific community use HeLa for short? except to keep valuable info. for themselves. They didn't want to credit the Lacks' family. Forget about the issue of a doctor legally accessing tissue that was to be checked in pathology. There was no trouble accessing tumorous cells after Henrietta's day. Not just any cells would do. As for the "greediness" of the family: someone looked them up for their DNA in hopes of understanding the cells' contamination issue. They needed more from that family.

    Posted by PaquiN on February 1,2010 | 02:57 AM

    Good story,nice,very interesting. I think the family should be compensated.

    Posted by Hannah on February 1,2010 | 02:58 AM

    Why is any of this not surprising? Has anyone heard of the Tuskegee Syphillis trials of the 1930s? It's part of a historical trend of scientists knowingly using the community to advance scientific knowledge. And yes, while it's great that we can all contribute something and make great strides in understanding complicated diseases- to anybody who says it's not about race- wake up and smell the coffee. Poor blacks historically have often been targeted unbeknownst to them- yet without any of the glory or compensation specifically because they were easy targets, often under-educated who wouldn't complain or present any obstacles in the reasearch or gain directly from the spoils of the findings. Henrietta L. and her family being a point in case. It's an insiduous form of racism and very pervasive. But- vive la scientific research and advancement and congrats to Henrietta Lacks!

    Posted by vanessa on February 1,2010 | 02:59 AM

    cells are naturally build to last its in the bible. however scientist could not explain why

    we die when our cells replacing each day to new ones. some will find it corny when the bible

    says the sin we inherit from Adam our generation dies. That does make a bad story. True its not a story. Thats what the Bible says. The original purpose of God is to create a Man and Woman to enjoy life forever and procreate. Did we ever ask ourselves why we only live in a limited time of 70 to 80 years? When God really instill in our minds that we are longing for infinite life? God made us to satisfy for a living but why are we suffering this things? We die easily as if life is temporary where in we view the imortality as an extreme? Or we could just say like this things imortality rather we say everlasting life as really natural cycle of life the first time God made Man? The Bible tells the truth. But many critisize and dont accept the truth. the funny thing is they cannot answer the question why we die. Just email me if you want the basis from the txt quoted from the Bible.

    Posted by jojo on February 2,2010 | 03:00 AM

    Very well researched and written piece indeed.I just wonder how much more Black contributions to world history and science the rascist scientific community has hidden. May i share this immortal thought ,"Truth crushed to Earth shall raise again from The ROOT for the Eternal years of God are hers,but error wounded, writhes in pain and dies among its worshippers."

    Posted by NAMAKANDO NALIKANDO SINYAMA on February 2,2010 | 03:01 AM

    It's about time.. History has serve it's purpose once again. The wait was long but Mrs. Lack's Family can be proud of their mother one more time and remember that it is never to later. It is your time now.. She has sent you a beauty gift. Her life is with you one more time. Be very careful with it. Enjoy it and remember Your mother's life has given many, many people a new life.
    Take care.

    Posted by Blair on February 2,2010 | 03:01 AM

    The outraged comments, ie. what they did to her, her family, what they stole, they got away with it because she was black, they should pay, etc. are too much.

    Yes, by todays standards the lab scientists would not take a sample from one lab to another without approvals. But keep this story in the context of the time (in the 50's they didn't know much about cancer) and place (a scientific lab). And in perspective, it was a tiny cutting of a tissue removed for testing her health and it was then going in the trash.

    They took it becasue they were searching for cells which would continue to replicate. They'd probably done this many times with samples from many other, black or white, patients. It didn't matter to the scientist if she was white or black.

    I'm grateful for the scientists for doing their jobs. She was coincidental. I'm grateful they found her cells, but she's neither a hero or a victum. She deserves recognition as a footnote in history, but not compensation. Her family has a right to be proud of her and their family genes. But we don't owe them any money.

    Posted by Bill on February 2,2010 | 03:02 AM

    Incredible story. Imagine your cells living on for generations. Amazing.

    Posted by Jon on February 2,2010 | 03:04 AM

    HEROINE! THE GODDESS OF THE CELLS! :D

    Posted by MARISSA LARIOS BALDOVI on February 2,2010 | 03:05 AM

    Great article! Looking forward to put this in big screen. This would be an interesting movie.

    Posted by Jennifer on February 2,2010 | 03:06 AM

    It's a very interesting story, but the real question is whether the author will do anything for the family or will they behave like the medical industry that took advantage of them. As the author has stated vials of this woman's blood and genetic information have not only been used for positive purposes but have been sold worldwide. When do we loose the rights over our own blood? She was a poor woman and her husband only has a third grade education, can you imagine life growing up for her kids without their mother? I am appealing to the author to do the same as the author of the soloist, and to at least set up a trust fund where a portion of the money made for telling someone else's story goes to the person the story is about or in this case the decendants.

    Posted by intre on February 2,2010 | 03:07 AM

    Should scientists be allowed to use any part of a human being without explicit prior consent?

    The ethical question of human rights to our own body and its parts (including genetic information) is very important. The comments on this story illustrate how people fall on either side of the fence.

    It doesn't matter that Henrietta might have taken ten dollars for her cells, or that she would have given them without a second thought. The point is ... she was never asked. She was treated like a "thing". And that was wrong.

    Posted by Mary on February 2,2010 | 03:08 AM

    It would have been so nice if what went on with the hela's family with their campaign were written. It's an amazing story.

    Posted by pol on February 2,2010 | 03:08 AM

    I am a cancer survivor...If the cells they took from my tumor are used to help someone else, great...As for the family being compensated, well how about giving them a job in one of those companies and some education to further their careers...Both of my parents died from cancer...What they did with their cells I have no idea, but if they are using it for research more power to them...To say they let her die because she was black is horrible...Look back at survival rates back then...We don't know what stage her cancer was...Bless her for her contributions and all though it was done without her knowledge, bless the doctor and the researchers too...Lets hope that this will be an eye opener and that all will realize the lives that were saved because of this...Also that the medical profession do things correctly so that controversies like this will never occur again...As for the family, maybe they could write a book about their memories and the daughter could share what she wished she could have had with her mother and what she would like to tell her...Also they could do talks on shows and share what their lives have been like...Maybe it would be a great eye opener for all humans to hear...

    Posted by Carmen on February 2,2010 | 03:12 AM

    This is a big step in science.The family should be compesated.A further study on her offsprings may be interesting if allowed.

    Posted by Muhang'u, Kenya on February 2,2010 | 03:16 AM

    I challenge the showbiz industry in a particular to the biggest hollywood movie makers, to please make this story in a real things that all nation can seen in a big screen so that we can all observe how the scientist can do to our lives. This is the amazing story i've ever read in my whole life.Jun - Phillippines

    Posted by Jun on February 2,2010 | 03:20 AM

    She was absolutely beautiful!

    Posted by Janienne on February 2,2010 | 03:21 AM

    This'a great story.Helps strengthen my belief in God the almighty.From dust he made Adam,and from Adams'ribs he created Eve and for those who don't believe in Life after Death,this is a small proof .You need not look any further.Now instead of us criticising and talking about compensations,why dont we open up a fund where all of us in America and indeed the whole World,could show our gratitude by contributing,each one of us,just a dollar to the family .ln my opinion this could be our way of saying thankyou to the late"Henrietta."We are Millions in America alone,and Billions in the world.Surely a dollar is not so much especially now that we know the truth about the HELA cells.Almost all of us have be immunised against "POLIO",had it not been for her--l hate to imagine this--we would have all,probably,been useless to each other and nobody could have been there to comment and/or criticise.

    Posted by OPIO OGUTA on February 2,2010 | 03:24 AM

    Interesting. Would love to read the book.

    Posted by Oma Erhariefe on February 2,2010 | 03:30 AM

    There can only be one remind of that movie.serious this is a great story If one the physician or scientist didn't take the cell then this wouldn't be a story something are meant to be and this was one of them.its like the saying if you wait long enough it will come out in the end.some of these people in this story when I hear there name it bring chill all over me,reason my decease mother carry the name Henrietta and I got a sister name Deborah and the funniest thing I live in West Virginia I don't know if that was just common names in the fifty's and I'm from and Africa America decent.I would like to know Henrietta maiden name.I think this story will get greater view then amagine.it should be all about the story and only in heaven you should get the real pay check.

    Posted by Joe D on February 2,2010 | 03:31 AM

    Adam Curtis of the BBC made a documentary in 1997 about Henrietta Lacks'cells and how they have transformed modern medicine. The documentary is called "The Way of All Flesh", and you can watch it on google video here

    Posted by laddermanjack on February 2,2010 | 03:34 AM

    Thank you for this very informative story for Black History Month. In response to the silly comments about "vampires", it's important to clarify that the cell line continues to divide (generation after generation), but the individual cells do not live forever. Regarding compensation, I don't know if the University/researchers "voluntarily" compensated the Lack family, but several court cases have determined that patients have no legal rights to the removed tissues/cells/fluids and have no claims to any subsequent commercial products. However, there are rare cases where advocacy groups have acted on behalf of patients to specifically negotiate compensation in exchange for their biological tissues/samples. So, it is not impossible to conceive of a way to get compensation directly or indirectly. BTW, if you ever participate in a clinical study, make sure you read the Informed Consent closely, because the use of your biological substances for subsequent research activities should be acknowledged.

    Posted by Gene Mason on February 2,2010 | 03:38 AM

    Thank you for enlightening us, we now have yet another UNSUNG HERO to honor. And really nice narration !! Keep writing.

    Posted by Das on February 2,2010 | 03:40 AM

    How do we know that the harvesting of her tumor cells was done without her consent? If only the doctor and the patient were in the room, she may well have given oral permission for the donation. Lots of people are willing to donate parts to science, even their entire bodies, without compensation, of course. Why is everyone so worried about the family being "compensated"?

    Posted by nbmd on February 2,2010 | 03:56 AM

    Amazing story, there's no such thing as "immortality" its only the invention oh human kind......it shows only " money is root of all evil".

    Posted by Marc on February 2,2010 | 04:03 AM

    Never knew about HeLa cells, just like I am sure the majority of everybody out there. The worls owes this woman a lot. I agree with Kelly, a movie should be made about this. Hope it is about the contribution of this lady and not simply about racism and money.

    Posted by Sarah on February 2,2010 | 04:07 AM

    Immortal Cells do not mean the cells they have today are the actual cells they took out of Henrietta. The cells they took from her keep dividing into new cells forever in a dish, that is what is meant by 'immortal.' So the cells they have to today are descendents from the ones taken from Henrietta. When scientists try to grow most normal human tissue in a dish, those cells will only grow and divide into new cells for only a few days to couple weeks before they are no good anymore...just thought I'd clarify that seeing some folks comments...

    Posted by CrumB on February 2,2010 | 04:07 AM

    That's great story!!!!!!!!

    Posted by Sarita on February 2,2010 | 04:22 AM

    this is an amazing story, what is great about it she save lives. henrietta larks, she gave life to mankind, at a time when science, was just discovering cures on a small scale.the polio vaccine they found, when science diden't know how to cures cancer,and gene expression was never throught of until then.cellometer vision, cell analyzing.optimizing your cell isolation,increase cells yield and viability,now there are over 1,000.000 ready to use cells.in 1951, the family was taken advantage of, by a misfortune of henrietta she had cancer,and if she had not,there would not has been no cure for polio vaccine the scientists treated her without concent,diden't give back to her family knowely they were poor.what ever measures her family took, they earn evey right ,because the HeLa cell came from their mother, and as a wife. it's call giving back. when something so very very great was so achieve from it.one hand ,washer the other. if that had been an invitro. the serigate mother carring the child, after the full nine month,of the delivery, the serigate mother would be paid in full check, $26,000.00 dollars. and half at the signing of the contract. and some want the child, after they carry it, for nine month, now! you have to go to court. why do you thank the serigate mother wants to keep the child?because she see a financally stable life.

    Posted by mary ragland on February 2,2010 | 04:22 AM

    her cells dont live forever...its just that these cancer cells have ability to produce the same cells by mitosis permanently, so the younger cells replace the older ones. normal cells have limited mitosis, their chromosomes get shorter each mitosis.once the chromosomes reach critical lenght, the cells can nomore divine.

    Posted by Luckatom on February 2,2010 | 04:38 AM

    People who jump on the "Racial" or "compensation" bandwagon are showing either their age or ignorance. At that time it probably was not unusual to send tumor tissue to "the lab" for analysis (even without getting consent) ..... it's called Pathology. Also, how do you know he didn't tell her ... if only in passing. It was not revealed if he "took" the cells via cervical scrapings, excisional biopsy, or if she had a hysterectomy. How did he know that the cells would be "immortal"? Maybe he didn't. He deserves much credit for doing what he did. People want to benefit from stem cell therapy .... should every egg and sperm cell donor be compensated millions if their cells happen to be the ones that turn out to be valuable. You speak of the cancerous cell as if they are "good", or if she wanted to keep them. I'll bet she, and her husband just wanted the cancer gone. While in a perfect world, the family would get noted or helped by the monies, the one who "deserved" to be "compensated" or "paid" had already died.

    Posted by isaaa S on February 2,2010 | 04:45 AM

    This is a great story.This should be in BLACK HISTORY MONTH,story about Henrietta Lacks, a poor black tobacco farmer whose cells was stolen from her cancerous body without permission. Scientists been trying to grow tissues in culture for decades. Her cells, amazing never died. It is sad, that scientists made billions from her cells. The family or offspring should get compensated. Thanks to the person who bought this story out. There are other stories that haven't came forth yet! Where are the Lacks family today? Is Rebecca Skloot giving the profit to the family? Do the right thing and you will be bless. Other was bless from Henrietta Lacks cell without her knowledge, her cells was stolen. I'm looking forward of buying this book.

    Posted by Rochelle on February 2,2010 | 05:40 AM

    really interesting and new for me.....i think the book needs to be read ....

    Posted by ashish on February 2,2010 | 05:49 AM

    Before the beginning of time, God had a plan for Henrietta Lack's life. He knew in 1951 that he would exhilarate her life's accomplishments through the heart of a sixteen year old girl, Rebecca Skloot. God saw the injustice and said, "I will correct the truth." The Bible says, if we hide our sin, God will shout it from the roof top. If we are robbed, God will recompense. It is no accident that this story was revealed during Black History Month, it was all in God's own timing. Glory to God who sees all, who knows all and who will correct all.

    Posted by Charon on February 2,2010 | 06:06 AM

    trying to make money from things like these have tended to raise moral and ethical questions........i suggest we keeping researching,but tread carefully....

    Posted by omoloye a.k on February 2,2010 | 06:11 AM

    I've noticed in the comments section, several writers are concerned that human cells can float on dust particles. Well, I got news for them: something like 80% of the dust in your house, floating or not, actually comes from human skin cells!

    Posted by Debbie2008 on February 2,2010 | 06:42 AM

    ugh, why would someone want to be immortal it disgusts me

    Posted by mailinh on February 2,2010 | 07:00 AM

    HELAVA article, amazingly research done on the writers part. As a Biology student myself my hats off to her for staying the course,this never would have come to light. A MUST READ BOOK,great work thanks. The cells were frozen.

    Posted by H. lee Remus Jr. on February 2,2010 | 07:19 AM

    This story is remarkable. It is unbelieveable that Henrietta's cells live on from decade to decades. I find this to be very interesting and yet very fabulous. Especially since she is a African american. I know that her cells will definitely be used for research to find the cure to cancer and many other viruses and so on. I am also glad that the daughter of Henrietta wanted to know more about her mother as well. It is nice to know that Henrietta's family will be known in history. It is also nice to know that this situation itself has tremendously made history.

    Posted by Raeshawn on February 2,2010 | 07:36 AM

    this is incredible news is it possible to have those cells put in to you so you could live forever and is she still moving

    Posted by mariama fofana on February 2,2010 | 07:48 AM

    Wow!...this article is very amazing!...

    Posted by Tongs on February 2,2010 | 07:49 AM

    "Is this for real and if it is, why haven't we heard of it before? Are you saying that the cells never DIED or that they were KEPT alive by the scientist?Or is this just to promote the BOOK?? Because it seems to be working. I don't have aproblem with that, just wanted to know...Is this serendity or....?"

    Scientists work with "immortalized" cell lines all the time. They have either been transformed in a petri dish so that they continue dividing without petering out, or they have already transformed in someones body i.e. cancer - and they have the ability to keep dividing - AS LONG AS THEY ARE GIVEN THE NUTRIENTS TO LIVE. They can easily be killed as any other cell type, with bleach for example. They will not start to go crazy and invade other people and cause cancer in them. Sorry this story has ended up scaring people. It is irresponsible.

    Posted by kristin on February 2,2010 | 08:02 AM

    "This was a great article. It is sad however, to know that any of us could have the same thing happen to ourselves or our families. We are not subjects to be used as doctors see fit. We are people and we must fight daily for our rigts and freedoms."

    Again, it is very irresponsible of this article to suggest that the rights of human beings are not being taken into account - laws have been put in place as science has advanced and there are now entire divisions of the government that are in place to protect patients rights as well as any person involved in any kind of research. Nothing is taken these days without a consent form. If you don't sign a consent form, they cannot (or should not) use your cells for research. Typically cells/tissues are donated for research with no compensation. However, there certainly are companies that pay for donated tissues, especially normal tissues. Depending on the tissue, it could be from $50 to several hundred dollars. Donors are not given a cut of any profits a company sees as the result of the research, which of course would be decades later usually anyway and involve multiple cell lines. Some companies process tissues and sell to investigators - both normal and cancer tissues.

    Several years ago, the government actually shut down all clinical trials at major universities because the human subjects protections were not being followed properly. Since then, things have really improved.

    Gosh, maybe I should write a book - but it wouldn't be so exciting to read about this! It is more exciting to incite conspiracy theories!

    Posted by Kristin Goltry on February 2,2010 | 08:17 AM

    I think the writer had every intention of magnifying the race implications here. "Poor black tobacco farmer"? I look at the picture of her and her husband and I see a very handsome couple of some success, she is wearing a nice fur lined jacket, and he is wearing a nicely cut suit and tie. They just don't look like poor farmers, black or white. I think it is wonderful this lady made such a significant contribution but am puzzled by the exploitation inference. If I had been in the same situation, and actually already have been, I would have gladly offered myself to the advancement of medicine. I'm sure this lady would have too. This whole thing is coloring the story in a bad light, even reading many reader comments, it is obvious that some people are turned off by the way it was presented.

    Posted by Donny Griffin on February 2,2010 | 08:25 AM

    While the family should be given something and that millions have been made by others the reaction of the family when it came to the money does seem greedy. I did not get that impression regarding the daughter. She should be give a proper place in history-it is well deserved. How many of the family have passed from cancer and how many are still alive?

    Posted by maggie triner on February 2,2010 | 08:27 AM

    Interesting is not the word nor the description. HaLa was the topic of conversation several years ago when several scientist were trying to prove the origin of HIV and the AIDs virus. I am interested in the book to see what value is placed on the deceptive work that the European world has and continues to prey upon what is called modern science. Henrietta Lacks story was plastered on the internet many years ago; then all of a sudden, the articles and stories disappeared. I hope this is not an attempt to whitewash the real story of what happened. This is a continuation of the Tuskegee Experiments all over again. By now non-whites should know what European scientist actual interest are.

    Posted by W. C. Johnson on February 2,2010 | 08:37 AM

    I would like to respond to William Thomas' post criticizing the author, Rebecca Skloot. He impugns her character by calling her "self-serving" and referring to her "artificial magnanimity" in writing the book. Mr. Thomas, do you know the internal motivations of Ms. Skloot? Can you read her heart and thoughts? Apparently you have appointed yourself as judge. Instead of assuming that her motivations are as stated in the article (namely, interest in a fascinating subject), you assume that she merely has monetary profit in mind. Did you do the research and write the book? Are you jealous of her royalties? She earned them. Or maybe (and more probably) you are guilty of reverse racism - that is, assuming that someone of a different race could never have the noble motives that you yourself have. Of course white people are always looking for ways to take advantage of blacks. Do you recognize reverse racism here? "First take the log out of your own eye, and then you will see clearly to remove the speck from someone else's."

    Posted by Sharon on February 2,2010 | 08:50 AM

    Outstanding! This should be in history and science books for the next generations. Great story, I'll email this to my kids. Thanks for the article.

    Posted by Trivian Lewis-Racy on February 2,2010 | 09:03 AM

    As an African-American woman, I tend to rather agree with commenter Marion Brown. Every day this nation and its media trots out Wurlitzer-volume propaganda that I and other black women are "worthless" compared to all other women, who are promoted in this order: white women highest, Asian women next, Hispanic women third, and everyone else after, with black women not even on the list, or at the bottom.

    Once again nature reminds the world black females are not worthless subhumans. This reminds me of the fairly recent scientific discovery that an ample backside may just keep women alive longer.

    I suppose like first our skin color (tans), our hair structure (perms), our backsides (first the 19th century bustle to copy then then 20th and 21st century media denigration campaigns to devalue them), and our lips (collagen implants), our cell structure will be next on the replication/denigration list, eh? Keep vying, folks.

    Posted by Karen on February 2,2010 | 09:09 AM

    Amazing to see all the different veiws!

    Posted by dman on February 2,2010 | 09:22 AM

    Nice Story,
    If I had the money, I would probably buy the book myself! It is great that the author empathized that "good" came out of the taking of Henrietta's tumor cells, despite that fact that the original doctor took them without her knowledge.

    However, with a the family being left in the dark about this for SO long. And with drug manufacturers & the medical community in general making literally Billions upon Billions of dollars on the discoveries they've made USING Henrietta's cells. I think some LONG overdue "Royalties" if you will are due this family. It is such a shame they have lived in poverty for so long while the rest of the world profited from their moms contribution to science.

    Many many people would of died with out the discoveries made with Henrietta's cells. So we are ALL indebted to this woman. It is such a crime that this family was left to live in such squaller while all the rest of the medical world profited by the discoveries made from this woman's body. A note to the family though, I would say don't take just one lump sum.

    Have the courts set up a "Royalty" percentage on all products made from your mothers cells. That way this will be a legacy that will be passed down through your family for generations, & should only get bigger & bigger over time as new technologies are discovered to be valuable from the use of her cells.
    God Bless you Henrietta!.

    Posted by Stu Hannah on February 2,2010 | 09:22 AM

    The Book is called "THE IMMORTAL LIFE OF HENRIETTA LACKS" by Rebecca Skloot. You can buy it at Barnes & Noble.

    Posted by Amy on February 2,2010 | 09:44 AM

    Quite uncanny indeed. Henrietta resembles me and I wouldn't be surprised if women of color were science subjects without them knowing because that's how scientists are. Their nature of inquisitiveness and fascination into the human world, especially when it comes to DNA, cells, reproduction. My mother died of Cancer (will be 15 years this April) and I had heard stories of how she had to be injected prior to her getting pregnant with me, so I would not be at all surprised if she had been injected with HeLa cells. Now that would be worth looking into, not only how the HeLa cells aided medicine with its discovery of cures, but how many were injected into women of color as a way of exploring and GENE MAPPING. I am going to investigate this if it takes me the rest of my mortal life.

    Posted by Coretta J Pruitt on February 2,2010 | 09:45 AM

    Very interesting story! Amazing...

    Posted by Emmett on February 2,2010 | 09:52 AM

    My grandmother had a breast removed, my mother had a breast removed and gall bladder surgery and my father had a cist removed from his neck, among other surgeries over the course of their lives. I'm almost certain, there were tests done on that tissue. Who should I sue, in order to receive the most "compensation"? Show me the money!!!

    Posted by Michael L Lewis on February 2,2010 | 09:54 AM

    Whether it's a right ot wrong situation,they all have to answer to God. Maybe they'll search their hearts and do the right thing. You thing?

    Posted by Jody on February 2,2010 | 10:08 AM

    Pretty sad how a great story about scientific research is twisted into some kind story of racial plunder.

    These were cancerous cells removed from her cervix in the '50s. After generations of scientists made use of the specimens, discoveries were made and treatments developed.

    And now, the greivance-minded boneheads translate this into cells stolen by whitey and just-deserved gains kept from the family. Pretty sad how every analysis must devolve to this kind of racist greivance-mongering.

    Why should her family receive anything other than recognition? She didn't invent those cells - it's not like she was a recording artist and her performance is being republished without royalties being paid to her estate. No, in this case the doctors and scientists salvaged a very bad situation (this woman's cervical cancer) into something that would eventually, after a lot of hard work by a lot of people, into something good.

    It's not like her relatives were being denied use of a bunch of cancerous cervical cells - they either went into a petrie dish or into the incinerator. The hard work of others was what made something good out of the bad situation.

    Posted by JSinAZ on February 2,2010 | 10:32 AM

    Nice article, I am very interested in reading the book for myself. However, the simple brushing aside of the idea that racism is not subtle and complicated misses the true depth of its influence.

    Posted by Steven Speight on February 2,2010 | 10:53 AM

    Great Story!!! I purchased the book yesterday. I want to know was the family compensated and when will the family appear of OPRAH!!!!

    Posted by Anita Shari Peterson on February 2,2010 | 10:54 AM

    What exactly should her family be compensated for? Did they do something to deserve compensation? Was this woman mistreated somehow? A tissue sample was taken. True she didn't give her consent, but she wasn't harmed at all! Where was the injury? Tissue samples are taken everyday, and no one questions where they are sent or how they will be used or disposed of after testing. This was not unusual or harmful to anyone. Rather than celebrating the fact that the samples were used to help all of us the family is bitter that they didn't get paid for something they had nothing to do with? I'm confused.

    Posted by Chuck on February 2,2010 | 11:01 AM

    Fascinating story. I expect to see it on PBS some day, on a program like Nova, P.O.V., or maybe even Frontline.

    Posted by Junkster on February 2,2010 | 11:12 AM

    Wow! Very Interesting I want to read the book. I do feel that the family living should be compensated for all the good that has come from the use of HeLa cells.

    Posted by TB on February 2,2010 | 11:29 AM

    Ms. Lacks was not uncompensated. She was treated at one of the best medical facilities in the world for free

    Posted by Michael on February 2,2010 | 11:46 AM

    There is a difference between doing the "right thing/saving lives" and illegally removing a human beings intellectual or physical property. Science has often crossed that line and been rewarded for it in the past by Government. Is it right? Is it okay for Doctors to remove an individuals cells without that donors "consent"? The Tuskegee syphilis study/Public Health Service syphilis study conducted between 1932 and 1972 in Tuskegee, Alabama, by the U.S. Public Health Service. Investigators recruited 399 impoverished African-American sharecroppers with syphilis for research of the untreated disease, in hopes of justifying treatment programs. The researchers/scientists intentionally misinformed all 399 patients about penicillin after it became available in 1940. Many individuals died, infected others and had children with health problems due to this unethical decision. A response from Doctor John Heller of the Public Health Service laboratory was that "The men's status did not warrant ethical debate. They were subjects, not patients; clinical material, not sick people." "The revelation of the Jewish Holocaust and related Nazi medical abuses brought about changes in international law. Western allies formulated the Nuremberg Code to protect the rights of research subjects. No one appeared to have reevaluated the protocols of the Tuskegee Study according to the new standards."

    Posted by william cordova on February 2,2010 | 11:46 AM

    Edward Drinker Cope (July 28, 1840 – April 12, 1897) was an American paleontologist and comparative anatomist, as well as a noted herpetologist and ichthyologist. "Cope identified four groups that displayed characteristics evidencing lower evolutionary status: the non-white races, all women, southern European whites (Jewish people and Italians included), and the lower classes within the superior races (Cope was particularly contemptuous of "the lower classes of the Irish"). The adults of inferior groups were considered throwbacks who remained in an arrested evolutionary stage, more like the children of superior white males." 1972-1976 US Government sponsored and directed The Indian Health Service in many Native American "reservations." Illegally sterilizing over 3,400 Native women without their knowledge or consent. Dr. Connie Uri, a Choctaw Indian Physician found out about the abuse and helped cease these operations. "In 1870, Dr. Sanford B. Hunt claimed that the average African American brain weighs five ounces less than the average white individual's brain, and the average mulatto's brain is smaller than the brain of an average African American. From this, Hunt concluded intermarriage between the races would produce inferior offspring. His studies played a role in justifying the need for segregated school systems. " The US Peace Corps assisted in sterilizing young Bolivian women in the late 1960s. The US Government played a key role in sterilizing women in Puerto Rico starting in 1937. Science, medicine can often bring out great changes but it can also be abused and used to condemn and misrepresent Race, Class and Ethnicity.

    Posted by william cordova on February 2,2010 | 11:47 AM

    Nice!how can we protect that kind of taking cells from somebody saying "Medical exam"?Did her family got what the deserve in all sapects??

    Posted by Abdi on February 2,2010 | 11:57 AM

    this is horrible!

    Posted by sand on February 2,2010 | 11:57 AM

    Very interesting story for the benefit of society but there should be more to it like the Lacks’ family being compensated. Nothing was said if they were. Therefore this is plain thieving from the start (stealing the tissue sample). The right thing now to do now is to compensate this poor family. It seems that they were being exploited because they are not educated and they are people of African American descent. Rebecca Skloot will be getting rich now by selling the book but she did her part. But it’s the reality of those poor people’s lives. I hope some smart lawyer delves into this story and see to it that the right thing is done for this unfortunate family. I am not black but I am a person of equality.

    Posted by Audrey on February 2,2010 | 12:04 PM

    Its a real great finding. I too used to teach about HeLa cell line in tissue culture, but could not find much details about it....Thanks to Rebecca Skloot for revealing it out.

    Posted by Dipti Chourasia on February 2,2010 | 12:20 PM

    Who paid the bill at the hospital. What documents did she sign? She was given the best treatment NO MONEY could buy. During the majority of cancer treatments, specimens are taken FOR THE BENIFIT OF THE PATIENT. If they are used elswhere in the support of humanity and medicine where's the beef. It's always about money and lawyers!!

    Posted by WALT on February 2,2010 | 12:29 PM

    As a member of the Lacks family, I read the article with more interest than most people. I have heard her story both at home and at school my entire life. She was poor, her family not well educated. But that was then. The story does say that the cells taken and made immortal were done so without her permission. Why are we not outraged by this the way we are by the Tuskeegee Experiments? I understand the medical marvel these cells offered, but stealing is stealing - regardless of the victim’s socioeconomic background. These infamous cells launched a multi-Billion dollar industry, with little if any money or credit to the unknowing inventor. If one of the Reese Farms relatives (Another poor, but white family from the same area in Virginia) were the victim, this would be a totally different book. That said I'd like to mention that my cousins look sharp in the photo. Dirt poor, but they were able to afford nice clothes, grooming and a professional photographer. Certainly they were not rich - especially by our standards today. But for the 1951 prejudice American South, they were holding their own.

    Posted by C. Brown, MD on February 2,2010 | 12:31 PM

    Ironically,"Blacks" have contributed/scarificed so much to make USA the "Land of the Free and Brave" yet on the other hand, Blacks are not free to enjoy THEIR FREE country. Blacks are still judged by the color of their skin and not the contribution they have made ..... from the "Farms to the Institutions." Thank you Henrietta continue to soar with the Eagles and your name (Family Name) will be etched in Black History. Retribution in the form of $$$$$'s is good but a Medical Research Institution embracing, the "Immortal HeLa" with High School students,pre-med and first year Medical Students be required to study/research HeLa Cells and its impact on the various Medical Break through in the Medical field.

    Posted by Eastlyn on February 2,2010 | 01:04 PM

    Fascinating stuff! Must read book and sounds like a great storyline for a movie. I will reserve judgement about any illegalities and/or unethical conduct by the doctor who originally took custody of Ms Lacks cells after I read the book. I think Ms Lacks' heirs would do well to consult a reputable lawyer to protect their interests here. Some good lawyers might represent them for free, given that any potential litigation would be high profile and get national,possibly global,media coverage.

    Posted by Danny L Edwards on February 2,2010 | 01:09 PM

    This story is for the benefit of all human been, and it's a story of one of us, as humanity; let’s go ahead and find something to help humanity to fight against Cancer and other evil diseases...

    Posted by Remy OLEMBO on February 2,2010 | 01:13 PM

    Simply wonderful

    Posted by Smith on February 2,2010 | 01:37 PM

    Makes me want to read more. Now I'm hooked.

    Posted by Melissa Davis on February 2,2010 | 01:38 PM

    This was a great read and will definitely be picking this book up. I have worked with HeLa cells for a long time now and only heard half-truths and rumors about the origin of the cell line. In fact I have some growing right now! It will be great to finally read about the history of probably one of THE most widely used cell lines. Some clarity for those that don't understand what immortality is. In cells, as they get older/divide their telomeres (chromosome protection) become shorter and DNA damage accumulates. When this happens the cell has mechanisms to tell itself to die (apoptosis). In cancer cells and transformed cells these mechanisms don't work properly or are lacking. This makes it so that the cell cannot tell itself to die and becoming essentially immortal. Don't get single cell immortality and multi-cell (humans) organism immorality confused!

    Posted by Kelley Geuscaulk on February 2,2010 | 01:47 PM

    Excellent article...I do think the family should be compensated, though. Those cells have become invaluable. The amount of good that has come from them is priceless. The fact that the doctor took the sample "without telling her" is deceitful and blatant wrongdoing. There should be consequences. I'm sure the doctor is deceased now, so payment to her decendents is the only right thing to do.

    Posted by Donna on February 2,2010 | 02:01 PM

    This article and the profound impact it implies made me want to buy the book (which I have ordered from Amazon). I have never heard of such cells and I have taken a few biology classes too!

    Thanks to Rebecca Skloot & Smithsonian.com for maikng this story available.

    Posted by Mike on February 2,2010 | 02:11 PM

    The cells were propagated by George Otto Gey without Lacks' knowledge or permission (neither she nor her family gave permission)and later commercialized, although never patented in their original form. Then, as now, there was no requirement to inform a patient, or their relatives, about such matters because discarded material, or material obtained during surgery, diagnosis or therapy, was the property of the physician and/or medical institution. This issue and Mrs. Lacks' situation was brought up in the Supreme Court of California case of Moore v. Regents of the University of California. The court ruled that a person's discarded tissue and cells are not their property and can be commercialized.

    Posted by C Wood on February 2,2010 | 02:12 PM

    I'm glad in many ways for the experience of this All reaching me here, and the awareness of how I/Us/All Humans are benifitting in one way or another, from one another... whether we realize it or not. To me it isn't just "that" or "this" which does/doesnt matter. Its "what" its all about that moves me: WE :)What WE ALL gain to learn in understanding Life as a whole, by expanding our minds/stretching our capacity to accept potential, to see outside our particular "box of sets," setting aside our "due" prIde(s), WE do open our hearts: for the simple purpose of knowing HOW to CARE, i.e. be aware of/in/to/from/for & towards the Life/cause & purpose... called Life Itself. 2 "juice" the TRUTH/"re~feelize" our Reason Being. 2 set free Life. Releasing from ourselves resentment cuz it bonds us against Life. Isn't Life really to PAY attention 2 Life? To me, that means responding 2 Life with Life, taking responsibility for~giving~that~which~gives~Life... Whether it be a chance, a hand, a consideration, a sense of security, hope(for human scientists of all varieties/for human humans of similarly authentic human stuff & cause for living as You & I,) w/overlapping layers of similarity occurring naturally w/ diversity: physically, conversationally, spiritually, within varying studies, families of family, macro an microcosmically. I Believe that Love packed into the stream of Life, wherever it comes from, however it comes, can be recognized, acknowledged, realized & expressed; creating WHAT consitutes The True Immortal Life that in some way, shape, or form, tangible and/or intangible, cellularlly, emotionally, scientificlly, elementally, Personally, Divinely, & other~WISE, IS Spiritual Evolution. I am just thankfull for it All, and that I Live in a time, place & state of being in which I have the opportunity to experience the contrast within this One thing and be able to choose to offer/express & share Peace, bottom line:) luv~N~light(Good Vibes+Wide Palate=Productive World)

    Posted by NuNu C. on February 2,2010 | 02:38 PM

    I understand that everyone would like Henrietta's family to be compensated. But, by whom? It's not like Big Greedy Medical Company is smoking a cigar, sitting on piles of cash, and handing out vials of HeLa cells in exchange for big checks. The original people that did the cell culture from Henrietta's tumor probably didn't get anything, either. Most of the research that is done on HeLa cells is performed by hospitals and academic labs. These are funded by research grants, most of which comes from taxpayer money.
    A "billion dollar industry" refers to the sum total of the research grants, most of which pay scientists (who don't make much, believe me). The cells themselves are largely obtained for free, passed from one lab to another.
    So, who will be writing these fat checks to Henrietta's family? Sorry for the bad news, but it just doesn't work that way.

    Posted by Schistosomiasis on February 2,2010 | 02:38 PM

    Amazing how when something like this is reported all the LOW LIFES instantly start yelling " lets SUE someone "

    If you go to a barber and have your hair cut, and a strand of hair falls behind a counter, can you SUE the barber for keeping some of your "cells" ?

    Blood cell samples, tissue samples, etc are taken all the time and when you go to a doctor or hospital, these 'tests' are done routinely. I have never heard of ANYONE wanting these 'samples' back.

    Posted by Ted Wilson on February 2,2010 | 02:59 PM

    I'm definately going to pick up this book. I always knew that deep down in my sole that Black people made greater contributions to society than those barely mentioned. The fact that scientist tried to cover it up confirms that there is a God and He declares that what's done in the dark, God will bring to light. Also the fact that the Lack family lived in poverty while people got rich from using Hanriaetta's cells is absolutely implausible.

    Posted by Adrienne L. Miller on February 2,2010 | 03:07 PM

    You can't ignore the racist aspect of this story. Billions were made and are still being made. Her family should have been (and should now be) compensated.

    Posted by Eliza Reed on February 2,2010 | 03:14 PM

    For those that are interested, No the Lacks family never received one red cent nor any recognition. I would have been happy if they would have put a trust fund up for any Lacks descendants to go to college. And for the person who said we are not entitled because people who donate their bodies to science don't expect compensation well there is a difference when one donates and when it is taken without permission. They have taken it upon themselves to not only steal but sell it around the world, so why shouldn't we make money too.....it's our genes!!

    Posted by LaDonna Lacks Johnson on February 2,2010 | 03:29 PM

    I am 46 years old and have never been so interested in science in all my life. Captivating story.My daughter who's a biology Major Tells my why she was captive by this story too. Paula

    Posted by paula stevens on February 2,2010 | 03:55 PM

    This article is so timely, given the work I'm doing in community-based participatory public health research. It literally puts a human face on the importance of being transparent and ensuring maxiumu safety and human regard for all involved in bio-medical and social research.

    Posted by Randy C. Rogers on February 2,2010 | 04:07 PM

    I was very move by the story. This would be worth getting the book to finish. As far as the family wanting compensation NO! This lady was admitted to a hospital and in doing so, she unknowingly gave doctor permission to try to help her find a cure. In the effort of trying, cells had to be removed and tested. So in respect to the family, their mother had given her permission to take her cells. After there removal, there the property of the lab. I think their mother would have been proud of her donation to the world. If anything help her husband gain an understanding of what happened, and how she benifited the world. The part of the family that thinks they should receive money,is just out for themselves and money hungry. Compensation should go to the donor if any, just as being done, by allowing her memory, name, or donation be told to the world. In this way she'll live forever.

    Posted by HC on February 2,2010 | 04:27 PM

    ‎[3] I believe the Tuskegee Experiment led to the discovery of the truth about Henrietta ‎Lacks in social literature and investigative reporting. In 1990's, President Clinton ‎acknowledged the racism involved in experiment and, I believe, gave some monetary ‎settlement to the surviving children of those who perished. In comparison, we have very ‎detailed literature on "medical experiments" on Jews in Nazi death camps (less on similar ‎German practices in Southwest Africa). We have no qualms calling Nazi actions of the ‎‎1940’s racist. White scientists harvesting cells and conducting death experiments on ‎blacks are "subtle and complicated." Not only is the Lack’s story an example of medical ‎racism, the author now intends to profits from their tragedy to sell books. I agree its a ‎story that must be told, but SHAME ON MS. ZIELINSKI’s insensitivity to the clearly ‎broader, racist implications within U.S. medical history. ‎

    Posted by B Brown on February 2,2010 | 04:41 PM

    ‎[2] I understand the danger of "litigating the past," but it necessary in this case to ‎underscore in no uncertain terms THE RACISM OF THE 1950'S FACILITATED THE ‎ACTIONS OF WHITE PHYSICIANS TO HARVEST MS. LACK CELLS. If readers ‎are not convinced of this, I would implore you to study literature on The Tuskegee ‎Syphilis Experiments. The revelation of a nearly thirty-year experiment in which white ‎scientists lied to poor Black Americans in the south in order to inject them with active ‎syphilis strand, study the rate of deterioration of their vital function, while refusing them ‎well-known penicillin until they died, was acknowledged in some press reports in 1970s. ‎

    Posted by B Brown on February 2,2010 | 04:41 PM

    ‎[1] Ms. Zielinski is clearly deceptive when she states near the very end of the article that ‎the Henrietta Lack Lack story "has often been held up as an example of a racist white ‎scientist doing something malicious to a black woman. But that's not accurate." I read ‎about Henrietta Lacks years ago, as a student at well-known historically black college in ‎the 1990's. A limited history of Henrietta Lack’s has been likely been floating in social ‎literature since probably the 1970's. Most of the literature I read on Henrietta was ‎considered "afrocentric" and probably dismissed in the “culture wars” during my college ‎years. ‎

    Posted by B Brown on February 2,2010 | 04:42 PM

    Why is that this did not make it to national/International news. We have rights to intellectual property but not to cells? Entire world has benefitted but nothing to her family?

    Posted by Wickrema Singhe on February 2,2010 | 04:45 PM

    Wow, very interesting indeed. I have never heard of such a thing and i am very intrigued on such a great find. what shocks me the most though was that these samples were taken over 60 years ago. i was just wandering if that was the only specimen found. If not how could we incorprot this to make humans immortal. Very very interesting indeed though.

    Posted by Tanner Stufflet on February 2,2010 | 05:08 PM

    Interesting. So, was any link to cancer picked up in Henretta lacks kids???

    Posted by Bishop on February 2,2010 | 05:52 PM

    Quite an interesting story

    Posted by ray on February 2,2010 | 06:08 PM

    Totally amazing! this makes me so interested since i'm interested in going into the bio-med feild. AH! totally awesome! I'd love for this lady to speakkk at my school or something!

    Posted by Tropicana on February 2,2010 | 07:33 PM

    THIS WAS A REALLY GREAT ARTICLE! I'm normally not so in to science, but this makes me want to learn more!!! Barnes & Noble, here I come!

    Posted by olivz on February 2,2010 | 07:38 PM

    henrietta was an amazing african american woman who was never known .most black people dont get credit for what the did instead caucasains do

    Posted by celeste on February 2,2010 | 07:39 PM

    Wow! That is really sweet! i hope i get an A+ on my0 report of this article!

    Posted by misshomework on February 2,2010 | 07:40 PM

    this is a beautiful story for black history, lack to learn more.

    Posted by beatrice alexander on February 2,2010 | 08:47 PM

    The Family never got any money from this. When I came across this story, I e-mailed my cousin, her husband is a close relative of Helen Lacks. Her contribution to the world is just amazing. It's just sad that this was done without her and her family's knowledge, or consent. I realize it was in the name of science, but there is a limit to when it is in the name of science and when it becomes a personal violation. To harvest someone's cells without consent and use it to make a profit is a totally unethical. The family should be compensated for the contribution Mrs. Lacks made to the world. When we look at the larger picture, Mrs. Lacks' contribution has saved thousands and thousands of lives around the world, and continues to do so. It would be fitting that her family get some type of compensation and She be given global recognition for her life saving contribution.

    Posted by Gloria on February 2,2010 | 10:17 PM

    wow, this is so fascinating

    Posted by david on February 2,2010 | 10:32 PM

    While many people or corporations may have made money on these cells after the fact, and I do believe the family should receive some compensation, no one who freely donates tissues or organs is ever compensated.So if HeLa had agreed to donate the family would not have been compensated. Since the cells were harvested illegally, the family surely deserves compensation from the Doctor and whatever entity he worked for. After that however, no one is really legally liable for using her cells.

    Posted by Bustakap on February 2,2010 | 10:50 PM

    Interesting article. I do not understand why everyone thinks this family deserves money. Enlighten me.

    Posted by Eugene on February 2,2010 | 11:39 PM

    I can appreciate the book. It is indeed an expose'. However, given the history of this country as it relates to stealing, inflicting genocide, and other devious acts, how does the purchase of the book help the family? This is not an attempt to discredit the author;however, how many more Black people have to be exploited? Her family should receive at least one billion dollars. After all look at how many unknown physicians have cashed in on this.

    Posted by Ralph Moon on February 2,2010 | 11:43 PM

    This story is fascinating in that it speaks to the beauty and simplicity of life. It is unnerving in that it harkens to a "Tuskegee Syphilis" experiment in the north east. To make an assumption that this was not done with any racial implications is unknown. However I would presume that race did play a role in the decision to not inform the family and the patient of this "miraculous and immortal" cell when one found that there was an opportunity for profit. There is a bit of unethical actions lurking here. I do hope that the family receives adequate compensation.

    Posted by Audra M. Akins on February 2,2010 | 12:09 AM

    what is more fascinating is the fact that Hela cell has helped advance human knowledge.

    Posted by Zak Kam on February 2,2010 | 01:41 AM

    The Immortal Life of Henrietta Lacks

    Posted by Raphael Bailey on February 2,2010 | 02:14 AM

    She was not "a poor black tobbaco farmer"; she was a poor black tobacco farmer's wife. PC nonsense.

    Posted by Richard Hawkins on February 3,2010 | 03:02 AM

    I do not think the family deserves compensation simply because a lot of money was made from this, or because they were poor. Those aren't good reasons. It would be NICE if they could be GIVEN some of the money, but they didn't do anything to earn it. The scientists and researchers did all the work. Also, the cells could have been taken from anyone, but they happened to come from this particular donor. People please remember this was done in the 50's before there were any laws or even ideas about privacy like we have today. What the doctor did was standard practice and was not "immoral" in that era. It's wonderful that the cells were able to help the field of tissue culture, but I wish the identity of the origin of the cells was not used to create a racial and financial battle.

    Posted by michele on February 3,2010 | 07:17 AM

    So MANY comments both positive and negative. I am the grandson of the scientist that RECEIVED the tissue from Henrietta, George Gey. My grandparents were pioneers in cancer reasearch. The fact that they were able to grow the cells and that so many advancements to cancer research were done as a result of HeLa is the focus. Remember when this ocurred it was a long time ago. Some of you paint this as researchers making big bucks. That was not it at all. My grandfather carried the cells all over the world in tubes, in a modified fly fishing case (he loved fishing) next to his body in his upper suit pocket to keep them warm. He GAVE the cells to any research lab interested in cancer research. There were no patents, no copyrights. Just amazing doctors helping each other in cancer research. It was never about money. Read the book, it's accurate and has much more information.

    Posted by David Greene on February 3,2010 | 07:32 AM

    For those of you who think Henrietta Lack's family should not be compensated because the HeLa cells were used for the good of science, then perhaps the scientists should stop selling the vials of the HeLa cells for $25 since it's "for the good of science". Fair enough?

    Posted by Victoria on February 3,2010 | 08:20 AM

    wow rich people took advantage of poor people... how shocking!
    Bet that has not happend to anyone else.(SATIRE)

    As for vaccinations and cancer treatments helping man kind, depends on which side receives the checks!

    1. Cancer is now the leading cause of death in the US
    2. Heart disease
    3. DOCTORS & Hospitals rank third
    Keep your 'magic medicine'!!!

    Posted by unsheepled on February 3,2010 | 09:22 AM

    I will be reading the story of Henrietta. I am a Research Scientist and as a Microbiology and Molecular Biology Grad student my research revolved around the use of "HeLa" cells. Please know that we were taught and well aware of the background/derivation of these cells to which we owe so much advancement in the field of Biomedicine.

    Posted by Gentry on February 3,2010 | 09:46 AM

    As a scientist who has worked with HeLa cells for years I find a lot of this article to be pure fluff and at times rather inaccurate. HeLa cells don't "float" on dust particles. Never. Mixing up and mislabeling vials of cells was the cause of the confusion about certain lines.

    Secondly, it cost money to grow cells and $25 a vial is probably less than the dollars spent to make the stock. No one is getting rich from selling HeLa cells for god sake.

    Third, in 1950 tissue sample were taken from anyone, black or white, because the idea of informed consent hadn't evolved. It is unfortunate but no one who donates cells today will profit financially if their cells become the next HeLa line. And there are hundreds of immortalized human cell lines today.

    Finally, I was saddened to read the level of scientific ignorance that dozens of these comments reveal. Everyone in our society to has a responsibility to get a handle on these issues so we can pass reasonable laws/regulations and not be driven into a panic by demagoguery.

    Posted by George L on February 3,2010 | 11:08 AM

    Wait a minute, what you think the medical information disclosure procedure is about?

    Beyond authorizing the medical personels to proceed with the information on one's behalf, such a leverage does not prevent them from doing evil to us... Medical practice is not only a scientific practice, it entails some morality, a lot of ethics unfortunately most scientists are not equipped with...

    Unchecked things of this nature undermine the trust that should engulf us when entering a medical facility... as a patient, do not put yourself in a position of weakness enough not to exercise your right to know about information pertaining to your health status and anything taken off You as part of the medical procedure... Ask and follow up on such lab works... have witnesses about what is being done under you...

    You may not know the practices but malpractices and associated evil conducts are foreseeable... Use your wits!!!

    I do believe that anything taken out of context for the purpose of material exploitation will never end up accordingly with one's evil plans... nature has a Unique way of claiming back what belongs to IT... timelessly so far!

    Demba.

    Posted by DEMBA on February 3,2010 | 11:58 AM

    There's so much ignorance here, it makes my head hurt. First of all, research scientists don't sell anything, they just do research. Typically they share resources like cells with each other for free- we get aliquots of cell lines from other labs all the time, for example. The companies that sell them are the ones that culture or "make" the cells. Second, doctors clearly had permission to remove the tumor, as that was part of her treatment. It's not like they strapped her down and stole her cervix. And third, once something is removed from your body and declared medical waste, like a tumor or a cyst or an infected appendix, it no longer belongs to you. It's like how police can go through your trash because you relinquish possession of things when you throw them out. Demanding compensation because your grandmother's discarded tumor ended up being useful to a researcher is ridiculous- she didn't own it, even if she did, those cells weren't worth anything to the family, and would never have been anything to anybody if it weren't for the work of scientists.

    Posted by Allie on February 3,2010 | 02:07 PM

    it is a very interesting story and I would like to know about her life. when did she die? did she die from the cervical cancer? the fifties was a very different time and era and things like this happened all the time. it didn't matter what color people were, it happened in the name of science. young people don't remember the times but it was a very different world. I have heard alot of stories that happened in the 40's & 50's and some people were hurt by these experiments, more then people will ever know. she was not hurt by this. whether they should get money from this is for the courts to decide. still would like to know of her life as the person she was. there weren't a lot of cures then for cervical cancer and sad that it took her life.

    Posted by bj on February 3,2010 | 02:55 PM

    "This really shows "IGNORANCE". This person doesn't realize that the cell was "taken" from her body without her knowledge or consent. It NOT the same as you throw it in the "trash". I guess i could go further and say the the word"trash" is aimed at the "poor black" woman. This book will make some money and the hospital has already made and will continue to make money on this. The natural thing to do is apologize , compensate, and thank the family for the contributions made from the cells of Ms.Lack. Also, the family may have the same cells in their bodies, and if they agree to be tested to find more cells like Ms.Lack and help with the betterment of mankind.

    Posted by Dayne in Japan on February 1,2010 | 08:11 PM"

    Of course they were taken with her body with her knowledge, how exactly do you think they got them? The cells were part of a tumor, removed during a biopsy. Same thing that's done today when you have a tumor. And after they're analyzed, they are thrown in the trash, because they are *medical waste*. The only thing she didn't have knowledge of was what happened to the cells after they were removed, when they were no longer her property.

    And if anyone else in her family has "these same cells" in their bodies, it means they have a very aggressive form of cancer. So yeah, not likely.

    Posted by Alan on February 3,2010 | 03:37 PM

    It is my understanding that when a surgery or biopsy is done the tissue or body parts removed become the property of the hospital or facility where the procedure was done. I believe that it has been like this "forever". I remember hearing a discussion about this on the radio maybe twenty years ago where people called in and put forth their views on this issue, which can be very controversial. I once signed pre-surgery paperwork, and there was a section which stated that any removed tissue becomes the property of the hospital. If the tissue is in fact the property of the hospital, then they can do whatever they want with it. If people feel that this is not right and that "donors" should be compensated, it would probably take the enactment of new laws to accomplish this. I don't know how I feel about this particular family not being compensated, because I think this has happened thousands of times to other families and they just did not realize it. How do you judge who to compensate and to what degree? Is tissue that does not turn out to be helpful to research become less valuable for that reason, or is all such tissue equally valuable because it all came from a human being?

    Posted by Patti Higgins on February 3,2010 | 04:28 PM

    Wow! This is an amazing story! Thanks for sharing it!
    Jaycee

    Posted by Jassonn Williams on February 3,2010 | 04:37 PM

    The story of Mrs. Lacks was eloquently and poignantly told in Mrs. Harriet Washington's (should be) seminal book, Medical Apartheid, published in 2006. There is a long history of the use of African-Anericans as medical guinea pigs, regardless of the spin given to Mrs. Lacks' "contribution". If you want to read about Mrs. Lacks (who at some point resided in Turner Station in Baltimore, Maryland) in a larger context, read Ms. Washington's book. There are several articles about her that predate the 1990's: "The cells that would not die", The Baltimore Sun, March 1981." The immortal cells of Henrietta Lacks", Reader's Digest, September 1986. Another article, "Her cells made her immortal", The Baltimore Sun, March 1997, and a more recent article(not cited)written in 2005, also express the sentiments of her family.
    The story of Mrs. Lacks had been told before Ms. Skloot's decision to write it in such a way that opened the family to criticism about greed. If doctors can have hospitals and wards named after them, if they can prosper from their innovations, why complain about compensation for Mrs. Lacks' family? And, for the people who are fond of accusing African-Americans of using the race card; remember, it was the card that they were dealt.

    Posted by J Edwards on February 3,2010 | 05:05 PM

    The family did get paid, with the polio vaccine ! Asking for money is goofy , just greedy. "lived in povety" .. who's fault is that?

    Posted by bob march on February 3,2010 | 06:05 PM

    This is very interesting; however it is very disturbing. It should be about human preservation and healing and the power of human life, but all I can see through this is this family being used and a legacy abused. How can you not see the color issue when you view the back story!?! Come on... You have poor uneducated black folk tissue being utilized and making money saving lives of the rich and the "white." This is disturbing and exciting all at the same time.

    Read people! There is more to this story!

    Posted by Janna Wright on February 3,2010 | 08:07 PM

    too bad this article is plagued with the writers own commentary, because her story is sad

    Posted by Matvei Alexander Rutzen on February 3,2010 | 12:44 AM

    Very interesting topic. I will be buying the book.

    Posted by Tracy Lee on February 4,2010 | 06:46 AM

    First: Immortal cells are not always cancerous; at the time, there was no way to generate an immortal cell line, so the HeLa cells were a huge step forward.

    Now we can generally create immortal yet non-cancerous cell lines by creating hybridomas, among other methods.

    Second: Cancer is not contagious. If these HeLa cells become airborne, they'll die eventually or be destroyed by your immune system (either active or innate). The larger issue is that they'll grow in just about any laboratory tissue conditions, so if you work with HeLa cells, you must be extremely careful not to cross-contaminate your other cell lines.

    Third: While it is unfortunate that the Lacks family suffered this injustice, in the grand scheme of things it is relatively minor, especially considering that what the doctor in question did was (in the standards of the day) neither morally or legally questionable. The removal of the tumor would have occurred regardless of whether or not it was shared, so this action incurred no pain, hardship or expense on Henrietta -- therefore, the idea that her family should be somehow compensated is laughable. It should be enough to know that her contribution has indeed furthered biological sciences and medicine by an untold amount.

    Posted by B Unger on February 4,2010 | 01:41 PM

    What an amazing article. I have ordered the book and can't wait to read it. What an outstanding book selection for Black History Month.
    As an African American who had an interest in science in school, but didn't pursue it in college I wish I had been introduced to Henrietta Lacks and her hardy cells.A Black woman with miraculous cells-WoW! I now know I want to know more about cell cultures.

    Posted by Crystal Pickett on February 4,2010 | 02:47 PM

    It is wonderful how the FATHER above takes care of us. Because poilio could've killed most of us and some of us wouldn't be born. GLORY to GOD. Those scientist did exactly what they were suppose to do. Out of every mess there is a miracle from above.

    Posted by Sergio on February 4,2010 | 02:53 PM

    Interesting article but limited journalism. Ms. Lacks was not a Virginia tobacco farmer - she lived with her husband in Baltimore area to which they'd migrated eight years from Virginia years before for work opportnities eight years before her interaction with Johns Jopkins that gave origin to HeLa cells. They lived in the Turner Station, an African american enclave in the city, that's noww a section of Dundalk a middle class area now ironically 90% white.

    Posted by Jorge on February 4,2010 | 03:21 PM

    This is totally incredible!

    Posted by Jay on February 4,2010 | 05:45 PM

    very interesting. but how can her cells be immortal? One part of the cell thory clearly states that all cells come from cells that have alredy been born. in other words all cells die but new cells are born. plus if she had immortal cells she would have to be immortal.

    Posted by Natalie on February 4,2010 | 06:26 PM

    I was fascinated when I came upon a brief mention of this story online and related it to a few coworkers that night. Almost immediately, one of my friends said, "We have a story kinda like that in my family, too; it was written up in Jet magazine back in the 70's!" Well, I told more, she told more, and somewhere along the way, we found we were talking about the same woman! Henrietta Lacks was my friend's aunt! And, no, the family was never compensated, but I imagine that's fairly standard as far as medical research goes.
    Amazon is going to get a HUGE order for the book from my workplace!

    Posted by B Baker on February 4,2010 | 06:36 PM

    I am absolutely fascinated by this story. I will buy the book. Have family members in the medical field and they will appreciate knowing about Mrs.Henrietta..
    Yes, a movie should be made about her life.
    Lets encourage such a project. Yes, I would like to know if her family received any compensation... Really amazing!!

    Posted by America Bible on February 4,2010 | 07:38 PM

    I REALLY don't get it, what did her cells do to help us?

    Posted by Sara F. on February 5,2010 | 10:38 AM

    If researchers and big Pharma agreed to treat people at a reasonable cost and with greater philanthropy the Lacks family might not be so focused on compensation. Instead the multi-billion dollar industry has not reached out or shown any compassion in providing care after profiting off this unfortunate womans tissue. Informed consent only and always!

    Posted by Wendell on February 5,2010 | 06:03 PM

    I just know that I am blessed to have had the chance to read about this story. I cant wait to get the book and learn more about Mrs. Lacks life. Also I understand about the *ownership* of the tissue BUT.. I also think that by this story coming into the light by a BOOK that the family should be given at least something. As for the person(s) saying who's fault is it that they lived in poverty... MAYBE before saying that they should have taken the silver spoon out of thier mouth and walked a mile in her or her family's shoes ( if they could aford them that is )And last of all we should all be gratefull that we have had a polio shot and quit pointing the finger at Black-White-Red-Yellow or Green.

    Posted by Anne on February 5,2010 | 01:07 AM

    My daughter passed away at the age of 37 after suffering all her liefe from a rare heart condition which the doctors had told us she would not survive for more than a few months. Many different medical students and quite a few doctors got a peek at her over the years and probably learned a lot from her. After she passed away I offered to the medical institution where she had received most of her care the opportunity for an autopsy which was gratefully accepted. Did they keep any of her tissues? I don't know and I don't care. If they did then I hope they learned something from that too. My daughter would have wished that. Did I ever consider wanting to be compensated for that? Did my daughter ever think she should be compensated for being a study subject, a "guinea pig" as she put it so inelegantly? For a few years she refused to be a study subject as she had gotten tired of repeating herself to ever new people. But after a while she decided that to deprive scientists of her rather unique condition and the knowledge that could be derived from it was selfish and did not help anyone, least of all herself. It was one of the visiting physicians who suggested that she might have an additional rare condition and although the other doctors considered the possibility to be very remote it turned out to be true.
    My daughter thought that as she could not hold a job or otherwise be what is called a "contributing member of society", if science could learn something from her, if only one other person could be helped from whatever the doctors could learn from her, then her life was worth something. The Lack family should consider that.

    Posted by Irene Weygold on February 6,2010 | 03:03 AM

    Very interesting and informative. Much as I'm thinking of just the wrong way the testing etc was done, I'm staying positive and thanking Mrs. Lacks and her descendants/relatives for that contribution to medicine.

    Posted by teresa james on February 6,2010 | 04:32 PM

    This is a great story. God has made all of us to contribute something to the world and make it better place to live whether, it's designing a car or being a craftsman of furniture, scientist/ biologist, teacher. Sometimes we are not compensated for our contibutions but GOD has the final say in everything. Thank you . May God bless you and guide you with the information to put into this book.

    Posted by Henrietta Hall on February 6,2010 | 09:54 PM

    I can imagine this book becoming a movie, starring Lynn Whitfield or a younger actress look-a-like. We need more information from HL's relatives who grew up knowing her before her passing. Perhaps through this form of media her family can be compensated.

    Posted by Jacqueline A. G. on February 7,2010 | 03:08 PM

    I believe that when God created man in the begining He Created us to live forever. But sin brought death to the body(flesh) that was never part of God's original purpose.

    Posted by Deryl Gamble on February 7,2010 | 06:35 PM

    This is a great story. Henrietta Lacks was a poor tobacco farmer, whom cells was stolen from her cancerous body. This is on time for Black History Month. Amazing, her cells never died, and billions of dollars was made from her cells. Henrietta family should get compensated. Where is the family? Is rebecca skloot giving back to the family, for the information they gave her on Henrietta and about her family. Where is her daugther(Deborah) and her sons? Alot left out. I want to buy the book, but don't want to be mislead.

    Posted by rochelle on February 8,2010 | 08:53 AM

    Wow. Great Article. Very Intresting. Decided to use it as the basis for my midterm paper.

    Posted by devon on February 8,2010 | 05:30 PM

    Thank you, we need stories like this, a human contribution. What a blessing to have had a human named Henrietta Lacks.

    Posted by te sim on February 9,2010 | 08:22 AM

    very interesting. you know, i knew that about cell research, but not about this person in particular. thank you for sharing.

    Posted by Valeri on February 9,2010 | 10:04 AM

    very interesting i'm going to buy this book fo sho

    Posted by pooh43 on February 9,2010 | 03:08 PM

    I bought and read the book. What a fabulous story. I have to say that I do think it was terribly wrong for the Lacks family not to compensated in some way. I hope your book may bring them some of the recognition they deserve. It seems to me that the only thing that hasn't been done to this family is for the major labs to sue the Lacks family for the wild-overgrowth of HeLa cells in their labs. But I'm sure that it is just a matter of time. Hyperbolic perhaps, but with the number of wrongs done to this family, I wouldn't be surprised. Thank you for shedding light on an amazing story and making us all aware that any one of us could find ourselves used in such a way.

    Posted by tara on February 9,2010 | 10:14 PM

    Some of these comments are ridiculous!!! Why should her family receive money? If it was a wealthy white person, no one would say they deserve to be compensated for helping others. I am a biologist and scientist work off grants from institutions and the government. And for the person who said everything living must die so the cells only outlived her; the cells do die, but tumor cells are able to reproduce themselves. The cells are dying but new ones are constantly arising. As long as the cells are kept on the right agar, the cells will live on. In current cells, HeLa cells are not all the same as many have undergone mutations. So HeLa cells found in one lab may differ in the genetics from HeLa cells found in another lab unless they both had been frozen without cell division occurring to allow for mutations.

    Posted by Dr. D on February 9,2010 | 12:21 AM

    In response to the comment from diana c. posted Feb. 1,2010.

    The photo of a well dressed Henrietta Lacks is of a happy healthy woman. Regardless of her econmic status, based on what she's waring in the photo. I respectfully wanted to mention what seemed the most obvious answer as to where the family's finances may have gone.

    Let us not forget, that Henrietta was being treated for cervical cancer at Johns Hopkins, when she died less than a year later. I'm sure treatment for cancer was as expensive in the 50's as it is today. I wouldn't be surprised if the family were left financially ruined after she passed away because it's still happening today.

    The advances in modern medicine made because of Henrietta Lacks leaves me speechless, but also concerned. That in our ambition to achieve these great medical break throughs we fail to treat people like human beings.

    Posted by RT on February 9,2010 | 01:57 AM

    Read this article last week and had to order the book that same night from Amazon. Got it Tuesday and it is EXCELLENT! I've got a couple books going right now, but it will definitely be done by Friday.

    Posted by TankzMom on February 10,2010 | 12:12 PM

    As a black woman I am extremely grateful for having learned this story. I believe this story should be brought to the attention of the masses so that people of all races are aware of the great contribution and legacy Mrs. Lacks has brought tothe world.

    Posted by faith cunningham on February 10,2010 | 01:17 PM

    I am extremely proud of the contribution Mrs. leaks has made to the world even if it was made without her permission. She has truly had the last laugh on the world of medicine that truly did not see her as a human being. A contribution that has help people of all race's, creeds and colors.

    Posted by faith cunningham on February 10,2010 | 01:28 PM

    This was a very nice and well constructed piece. Nice job!

    Posted by Robert on February 10,2010 | 07:03 PM

    If you enjoyed the article, then read the book. I bought it yesterday and I am more than half way through it! In the 24 hours since hearing about the story on NPR and starting to read it, I have recommended it to at least three people.

    Posted by Caneriver on February 10,2010 | 07:30 PM

    I bought the book three days ago and am nearly done! It's fabulous!! Everyone who reads this story and is intrigued with the family and story, please note that Rebecca has set up a foundation to provide money for the education of Henrietta's family: henriettalacksfoundation.org (what an appropriate name!) Please contribute.

    Posted by Barbara Pokela on February 11,2010 | 11:23 AM

    This is a fascinating story about life and what God blesses mankind to discover. Unfortunately it sometimes boils down to a racial issue because people make it so. The bible tells us that God made everything and everyone so what we gain is from Him. Lives have been saved or prolonged and the research continues based on what this woman gave by an unknown donation. That the fact that it has been revealed should allow the family at least some compensation even if it is just her name being revealed and getting credit in the annals of Black History. Also to the idiot, who used the term "jungle bunny" I hope and pray that you or your family never have the need to benefit from the "HeLa" cells, and if you do, you need to fall down on your knees and thank God and Henrietta Lacks, a Black Woman for being a part of saving the live or lives of that person.

    Posted by Directornmmbc on February 11,2010 | 11:50 AM

    what happened to the cells in space?

    Posted by funnybunny on February 11,2010 | 10:02 PM

    Scientists wanted to study cancer cells, but they died too quickly. In Henrietta Lack's case, the cells not only lived, they thrived and replicated faster than any the scientists had ever seen. They were able to share the cells over and over again in many countries, and because they continue to replicate, the ones in existence now are more or less clones of the originals. As for the person who feels her family should not benefit, why not? The entire world is benefitting from it; and if you want to make believe some big pharma hasn't profited because of it, then you live in an alternate reality. They should be compensated, and compensated well; their relative, whether unwittingly or not, did and continues to provide valuable information toward various cancer research projects.

    Posted by deprogrammed on February 12,2010 | 05:21 PM

    this lady was a life saver. she should never be forgotten.

    Posted by tony g on February 12,2010 | 10:03 PM

    The real irony is that since some in the family can't afford health care, they can't benefit from the scientific advances that came from their mother's cells.

    Posted by Larry on February 14,2010 | 03:39 AM

    Two very sad take home messages. A 30-year-old gets cervical cancer and dies young. The tissues was taken without her permission. Now that the story is known some compensation should be made for the latter. If this was all happening today someone would be making $.

    Posted by Pat on February 15,2010 | 09:55 AM

    This sounds like a fascinating book. Ethical treatment of research subjects is a hot topic for anyone involved in research. I plan to read it.

    Mrs. Lacks was not a victim of racial discrimination, but of the "doctor knows best" mentality common sixty years ago. Many patients at that clinic had cells taken to that lab; Mrs. Lacks' cells just happened to be unusual. That said, there is a shameful history of discrimination and abuse in research. Tuskeegee is one example. Nazi torture in the name of science prompted a sweeping international change in standards for research in human beings.

    Most researchers truly do want to do the right thing. The problem sometimes lies in the shifting nature of what we see as "right."

    Posted by Sue T. on February 15,2010 | 10:17 AM

    That so sad

    Posted by Bob on February 15,2010 | 09:59 PM

    The story of Henrietta Lacks is one of an American science establishment which failed to live up to the Nuremberg Code we so famously set up for the rest of the world (and the Helsinki Declarations which built upon it). Henrietta Lacks and her family should have been granted informed consent to the research which proceeded on her cervical cancer tumor cells.

    However, shelves in tumor registries all over the world groan with similar samples from millions of cancer patients (including mine - I have a rare sort of cancer which grows on nerve tissue). Neither I nor any of these other cancer patients were given an opportunity to control the disposition of our excised tumors. I feel badly that the Lacks family has this sense of having been treated badly but they have not been singled out (apart from their relative's undeniable heritage in those unperishable cells).

    Posted by loupgarous on February 16,2010 | 07:09 PM

    I stopped reading the comments because this went from being about Henrietta's cells to a black and white issue. It seems to me that her name wasn't revealed due to the lack of permission to take her cells and greed over the money being made from her cells. White people are the only ones ever pointed out to be racist. And pardon my childish statement, but it takes one to know one. A non-racist doesn't see the racism. There was something truly special about Henrietta and I see her as a remarkable woman that unfortunately without her permission, touched many lives. I see her much more than just a black woman.

    Posted by Melinda on February 16,2010 | 01:37 AM

    Her family had every right to money made from the sale of their family member's cells.

    Posted by Nora C on February 17,2010 | 04:53 PM

    Immortality.
    Ethics.
    Humanity and its inherent drama.

    This story touches on all these themes and if you are looking for a good read, this should top your list.

    You'll be thinking about it, and talking about it, as I have been, for months to come.

    Posted by Michael Spurlock on February 19,2010 | 03:33 PM

    The only way I see it going down is to file a suit for emotional distress. Finding out something of this magnitude about your own Mother would be life-changing and could be very upsetting/confusing especially for someone religious who believes their Mother is 'living on'. For that alone, some compensation should be given but who determines the amount? It's like trying to figure out what to pay Native Americans for money lost for their lands held in Trust. It's impossible, but something is better than nothing. What would make me more upset is that my Mother changed the world and yet her name was never spoken. That's the true crime. Give the woman her due

    Posted by Lily on February 19,2010 | 12:22 AM

    This is a very sad story, for racism still remains center front in our society today. Had Mrs. Lack's pigmentation been of the dominant race, there would be no discussion because she and her family would have received recognition and monetary compensation they so rightly deserved.

    John Hopkins is known for exploiting African Americans. He La cells put John Hopkins on the map to academic excellency,ranking them number one in research and technology. I am sure that He la cells generated billions of dollars over the decades. And now Ms. Skloot will also receive millions for the sell of her book. Although Ms. Skloot has set up a foundation for the Lacks family (so she says), she [Skloot] will remain in control of that Foundation. If she really wanted to help the Lacks, she would have used some of the proceeds from the sell of her book to help the Lacks family. What is 5 cents per book? Like John Hopkins is Ms. Skloot exploiting the Lacks family?

    Posted by MESSA on February 20,2010 | 11:34 PM

    I feel very bad for her family cause they should get a piece fo the cake, anyway it`s a wild world and only the strongest survive.My admiration goes out to the writer for unfolding such a treasure, well done.......

    Posted by gala on February 22,2010 | 06:40 AM

    Excellent Story! What a beautiful woman! Her name should live on forever; even though she did not give permission. Her Family should receive some type of award. Thank You Henrietta! for the life you have given to so so many.

    Posted by Little Bit on February 22,2010 | 08:59 AM

    I am appalled and saddened at the 'reverse racism' in these comments. No one owes her or her family anything. All tissue removed today is required to be sent off to labs for testing and they can do whatever they want with it. At that time, no permission would have been necessary. I am so tired of people wanting to go back in time and apply today's standards to yesterday's actions. This family was in no way harmed by this scientific research. Third graders today have a better grasp than most of the commenters here that the cells used (sold) today are not the same, identical cells taken from this woman. The article clearly states they have been grown, cloned, etc., in labs for decades of scientists to continue more and better research against diseases. The 'profit' made by selling these generated cells helps fund the cost of more and different research, including production of more cells to use in experiments. Scientists and research companies are not zillionaires. If the commenters here bothered to know their history, they would know there are thousands of stories like this, where people contributed to science with out compensation or necessarily knowledge of their individual input. It is certainly not a color issue anymore than it is a gender issue.

    Posted by Ginger on February 24,2010 | 09:44 AM

    I'm wondering about the impact this story will have on African Americans who already feel disenfranchised from the American health care system. This issue speaks to the basis of why many Blacks do not have trust for their health care providers, the government, and/or White America in general. It's paternalistic to think that she didn't deserve to be informed that her tissues were being sequestered and it's downright racist to have profited so greatly from her tissue without having at least given her family an opportunity to recognize the contributions her unfortunate physiology made to science. It might have been nice for the family to know that they, too were at risk for having these abnormal cells and dying prematurely from cancer. First, "do no harm," right? Had it not been for the modern researchers interest in her family's DNA (probably for further exploitation purposes), they may have NEVER known about their grand/mother's contributions. This story makes me shudder to think of all that we don't know that's happening behind the scenes in research.

    Posted by Candace on February 25,2010 | 02:50 PM

    that is so cool!!!!

    Posted by Lesley on February 26,2010 | 03:36 PM

    I'm wondering...did the family receive compensation of any kind?

    Interesting story.

    I was a nurse & obviously interested in cell research.

    So many unanswered questions remain yet.
    Poppie

    Posted by Poppie on February 27,2010 | 05:40 AM

    That was a great article I loved it I think that this kind of science is amazing!!!!!!!!!!!!!!!! <3

    Posted by Nina Lewis on February 28,2010 | 10:05 AM

    "Can the family of H. Lacks file a lawsuit against the scientist? -Posted by C. Frazier"

    Who is 'the scientist'? The medical doctor who did everything in his power to save Henrietta Lacks's life? The many doctors whose research was used by Mrs. Lacks doctors to try to save her life?

    Or maybe they should sue every medical doctor who may be alive today because of Henrietta Lacks's contribution to medical science.

    Should they sue everyone alive today who did not die from polio because of Henrietta Lacks's contribution to medical science?

    Posted by Beyondken on March 3,2010 | 10:23 AM

    For everyone saying why is this about money and it should not be. Can I take something from you without asking just because it is interesting?

    Posted by Karen on March 3,2010 | 02:22 PM

    Wow unbelievable!!! We as a people have contributed more to this society and the world than folks will ever know like the holy scriptures spoke about in Deut Chp 28. I hope the family was compensated for this to the nth degree and should continue to receive lifetime royalty checks for Henrietta's cells that the medical community will continuing using for the sake of medical achievements now and in the future as a result of taking Mrs. Henrietta Lacks cells without her consent.

    Posted by Sande on March 3,2010 | 05:48 PM

    I am reading the book now and suggest everyone who has preconcieved notions about this being Johns Hopkins preying on African Americans, or anyone else for that matter, read it as well. It is definetly a hard to put down read, so having said that I think I'll get back to it.

    Posted by Anne Wilson on March 4,2010 | 03:58 PM

    This is clearly a case of common sense. Mrs. Lacks cells were taken from her while she was in the hospital without her consent. Right? Because of what the doctor or doctors did has aided the medical in curing and helping others with diseases than Mrs. Lacks survivors should be compensated and it should be done with all deliberate speed.

    Posted by linda tart on March 7,2010 | 10:35 PM

    I've worked with HeLa cells and cells from others that died of the diseases that produced the unique cells. Hers must have been a horrific cancer to produce cells that are nearly unkillable.
    I, and other scientists, marvel at the gift of these cells. We remember the people who gave up these cells even when we know little about them.
    Most people who give up cells are not compensated. I don't know if this right or not. How can we calculate knowledge? At least the cells help us find treatments that can help others in the future.

    Posted by Edobrinen on March 8,2010 | 07:00 PM

    I heard the Author talk a bout her book in NBR radio. And to all those people who are asking if her family got any compensation...The answer is NO...They didn't get a penny..Not only that but they don't even have health insurance.

    Posted by Sammy Adam on March 8,2010 | 12:29 AM

    Like so many others, I cannot understand why so many people believe the family deserves any compensation. The cells were given for study, and out of that many amazing things happened. The study of medicine was advanced and probably many people benefited. And just because they don't have health insurance doesn't mean the family wasn't treated.
    I don't see any correlation between Henrietta's cells and any issues with her family.
    The comments almost ruin the beauty of the message

    Posted by John on March 15,2010 | 02:59 PM

    It takes a vast amount of work and resources to grow, store, maintain, ship these cells. And, if you read the book, you will learn that the scientists who originally harvested and grew Henrietta's cells in their lab, did so with little support other than their own ingenuity. Sure, they have been bought and sold many times by many labs and companies at a profit for others. But the real value lies in what they offer scientists, many of whom don't really make that much money considering the value to society that their work generates. I for one will be donating my entire body to science when I die. I don't expect my family to be compensated. If someone down the line figures out a way to use my cells to 1. do good for all mankind, and 2. make a bit of profit, so be it!

    Posted by Amy on March 17,2010 | 04:52 PM

    In regards to the comment left on 3/15/10 by John. Ms Lacks cells were not 'given' by her, they were taken unbeknown to Ms Lacks or her family. - And everyone seems to forget. The 50's as well as before the 50's Blacks, in this country, by law, or lack of- had no civil rights..doh! (is pre MLK). So civil rights - personal rights, compensations, was unheard of especially in the South.(And for sometime after as well). FYI... During those times, and I'm not sure of when this changed over, but for persons doing at kind of work,it was called 'Share cropping'. And when parts of the family had to travel to where the work was, Migrant workers'. That term I believe still is used.

    Posted by A Dorin on March 17,2010 | 05:37 PM

    Posted March 17, 2010 from A Dorin

    Thank you for correcting the comment left 3/15/2010 by someone who read the story and still decided to use the word given or donated. The facts are this was an unauthorized taken from Mrs.Lacks, so for anyone that truly believe in their hearts that the family shouldn't profit from progress and success of Mrs.Lacks Cells(DNA).

    Well would you denied the family the recognition they so truly deserve also?. I speak for myself and many the family should profit from the cells some how. Someone wrote we don't understand that it took time and money to do this and that but reality is they what ever they put into it they double, triple, quadruplet that profit so they can't complain.

    What we are saying it has changed the medical world, and the family deserves to profit and be recognized from the great contribution from there mother.

    Posted by Deborah on March 19,2010 | 05:19 PM

    This piece is very interesting. I felt good knowing that yet another african american contributed to the future of the United States' future. Although it wasn't in a very good way, I still liked the fact that my ancestors contributed to a better life for everyone. It's sad that the family only wanted to participate when money was involved but I'm glad they eventually came around.

    Posted by Montrice White on March 22,2010 | 12:24 AM

    This lady's preserved cells have contributed to the onging knowledge search for the betterment of all human beings. How fortunate that testing and research have moved forward, although her family wasn't in the loop. Would that every family had the opportunity to be useful for the human family.

    Posted by Nancy Miller on March 24,2010 | 06:09 PM

    I have read the many posts here, to include but not limited to the many books on Henrietta Lacks. This NEW book is nothng but a shame to the real truth. There is nothing new in this book, at all. I personally knew Deborah, and was a researcher who interviewed many of the doctors that this author never knew or interviewed. The point, there is too much of the Henrietta Lacks story and medical history or mystery, that when the next publication comes out, there should be no shock, that serious crimes had been committed. No one is going to jail now, but, the real story shall be told, and you current view of Johns Hopkins shall or may not be different. One can assure you that, what comes next shall have the world on the edge. BELIEVE IT!

    Posted by Dr. Keith on March 27,2010 | 12:58 AM

    I just finished reading the book and strongly recommend it.

    Posted by Giuliano on March 28,2010 | 02:12 PM

    Crazy stuff there

    Posted by on March 28,2010 | 08:26 PM

    I just finished the book. It read more like fiction than non-fiction. I'm a 47 year old man and I was blubbering like a baby as I finished the book. I recommend it highly.

    Posted by Frank on March 30,2010 | 12:14 PM

    The Family of the late Henrietta Lacks should be compensated. The Supreme Court needs to see to this.

    Posted by Sharon on April 7,2010 | 10:00 AM

    Just found out today. Read the original story posted by Janet Singleton. Just wonderful. As a cultural anthropologist,I would have to agree that the political climate allowed this to happen,there is a thin line between the "racial" implications and the general government use of their 'subjects' for unauthorized experimentation.

    We do not ascribe to the common thought of race as a separate distinct and discreet genetic corpus. We do not share with the world that we currently only recognize one race. Human. You may read The American Anthropological Association's Statement on Race.Please.

    We are aware of the social constructs for political purposes. There are errors in thought and perception on some of the responses but that is to be expected.

    The writer, if she continued her studies in genetics would have discovered that the issue of "race" impacts only insofar as the perception. While it is not "real" it is a reality.

    From a humanistic perspective her cells have helped many. Please keep in mind that no society,group or clan has ever been exempt at one time or another from man's cruelty to man.

    I taught at The Borough of Manhattan Community College,2001-2003.

    Posted by Prof. Rosell Fernandez on April 17,2010 | 03:49 AM

    hi.... I m a research scholar and working with HeLa cells. Its really great to read something like this,because most of the times we keep on proceeding with the things without knowing the actual fact..thanx a lot to throw light on our knowledge. now i can tell my students the Fact of Non dieing cells.....

    Posted by Pooja Singh on May 2,2010 | 06:20 AM

    Her family should at least get some stock in the Big Pharm companies.

    Posted by Popo on May 5,2010 | 06:05 AM

    This was an interesting read. It is funny how one does not hear about such things unless one really digs into it. It is good that they were able to create vaccines etc, but lets be honest what these doctors did was only a little better than what happened at Tuskegee. These researchers should not be pated on the back for what they did it was completely unethical and immoral...But it was a means to an end! Her family should without a doubt reep some of the benifits of what was done.

    Posted by Marshall on May 7,2010 | 01:02 PM

    This story is both sad and intriguing.Someone needs to contact Oprah Winfrey to turn this true story into a movie.Henrietta Lacks family needs to be compensated for what has happened to their mother.Her cells were remarkable in that the cells helped save millions of people.And now it is her families turn and time.This is indeed a remarkable story.It keeps you wondering about what will happen next.I would love to read the book.I need to buy it soon.Thank you Rebecca Skloot.If it were not for your curious nature as a 16yr old.I never would have learned about Hela.Congratulations on a book well done.Please continue to write more true stories.I loved the story.Please write more.Maybe they will be compensated.Maybe not.But thanks for sharing this story. :) :)

    Posted by Teresa Winslow on May 10,2010 | 04:01 PM

    for anyone who doesn't believe this is true, George Gey was my great grandfather, my dad worked in the Johns Hopkins labs with him when he was a teenager. I think that this research is world changing, and I am doing a project on him in my AP European History class. I hope that a lot of people spread the book around because it is valid information and it's beneficial to know and be aware of this amazing discovery that has allowed for so much more research to be done, as well as the polio vaccine to be created. Thanks for reading and educating yourself :)

    Posted by Virginia Greene on May 11,2010 | 01:41 PM

    I read this book twice. I love it and I agree the lack's family should be compensated! From reading about the conditions they live in today, it is a shame that they were not taken care of after one of their own helped the world out in such a tremendous way. Thank you lack's family!!!

    Posted by Michele on May 13,2010 | 01:32 PM

    This is a very interesting article and I too will love to read this book. It is educational in that it shows the unknowing contribution of a Black woman to science and the study of cells and how to eliminiate disease. I wish her cancer had been studied at the time and maybe her own cells could have been used to save or sustain her life a little longer. I was born the next year, 1952, and I know no one knew how to treat cancer; just to let a person suffer and die. Thanks for revealing another part of Black history and the contribution that we have made and still make to science. I am going to be nosy and see what other contributions, I already know the majority of them, our cells have impacted on the scientific world.

    Posted by Gwen Freeman on May 14,2010 | 08:50 AM

    A very interesting story, Thank you <3

    Posted by Nene on May 14,2010 | 10:44 AM

    It is my belief that HeLa cells are the very reason that cancers have increased worldwide over the last half century. These cells are not "human" but a hybrid with 58 chromosomes instead of 46. They are as much viral (HPV) material as human. The ability of these cells to propagate themselves is astounding and they have already been intentionally incorporated in so many medical treatments and infiltrated so many cell cultures around the world that we are all potential hosts. DNA tests should be done on ALL cancers today to determine the level of HeLa DNA in cancers around the globe.
    The results will shock many people.
    Hentrietta is more akin to Typhoid Mary than a saviour.

    Posted by mick on May 18,2010 | 04:27 AM

    Some of the replies here are astounding. Please do some reading on the science behind cell research before jumping to ill-informed conclusions and making ignorant statements.

    A few comments...

    You leave your cells, and therefore your DNA, everywhere you go. Every time you touch something, sneeze, breathe; every time anything you've touched touches something else is a potential for contamination with your cells. If you've ever had a cut or abrasion, you've left white blood cells and epithelials on the thing that broke your skin, anything on which your blood fell, on the bandages that you used, down the drain you used to wash up. I say this to point out that there is no practical point to being paranoid about your DNA.

    Incidentally, you share the vast majority of your DNA with other humans (not to mention all the sequences shared with OTHER SPECIES), so most of your DNA is NOT uniquely "yours" anyway!

    Secondly, you do not "get" to profit from your cells. It is illegal in many places to sell human tissue. The value is placed on the results of research; the work, knowledge, expertise, interpretation put into generating those results. In and of itself, a human cell is financially worthless. While it is a sad irony that Henrietta Lacks' family is living in poverty, their situation is not any different from the millions of other people on this planet who do the same. They themselves contributed absolutely nothing to the research done, or the results or advances obtained from that research. Whatever outrage one might feel at their unfortunate circumstances, the idea that they "deserve" anything from the work that others have done is ludicrous.

    Were abuses committed by medical professionals and scientists in the past? You bet. At least, by today's standards. But what was "done" to Henrietta Lacks is not even remotely close to "abuse" even by today's standards.

    Posted by Jeb on May 24,2010 | 10:14 AM

    the issue of compensation has to two with a few things:

    1 - the cells were taken WITHOUT consent

    2 - the efforts thereafter to HIDE HER IDENTITY (if what they were doing was totally ethical, why not credit her properly and tell everyone what HeLa truly stood for instead of creating FAKE NAMES?)

    3 - in the era which this occurred, unfortunately it was common for African Americans to have things stolen from them without their consent and not receive any kind of credit or compensation

    4 - separating the identity of HeLa from her cells did a disservice to the scientific community because i'm sure at first there were many researchers that didn't have a full understanding of what made the cells so special - especially if using them became so commonplace

    5 - as was stated above, to produce cells at that rate, there had to have been one powerhouse of a cancer that she had and to use it for research is one thing but what about if/when those cells are used in other people or other living creatures? do they not have the ability over time to adversely affect the dna of others over time? i'm not talking in the short term. i'm aware in the short term they have helped to understand many diseases but it's still something that should be addressed.

    Posted by nat on May 25,2010 | 07:40 PM

    I have just finished reading this book. So very well written. I am so pleased to see a book like this emerge from a writer who cared about her subject matter. Congratulations.

    Posted by carol lorac and bruce abbott on May 30,2010 | 08:45 PM

    Did they find the reason why the cells could multiply indefinitely??Is anyone looking??

    Posted by John on May 31,2010 | 05:59 PM

    Fascinating book and well written. I truly believe that if Henrietta Lacks lived long enough to understand the effect she had on the medical world, she would take pride in the thought that her illness was going to result in medical advances that would help all of humanity. It was obvious that her personality was one of compassion and kindness. It is interesting to reflect upon any serious illness you or your family has been affected by and “google” that illness alongside HeLa and see how Henrietta’s cells benefited all of us. As an individual who has tested positive for a mutation to my BRCA 1 gene and a breast cancer survivor, I thank Henrietta Lacks for her contribution to the scientific community. As an individual who was invited to take part in the planning of a website about the Human Genome Project at NIH to be used by the public, I think Henrietta’s contribution to science is something we should all be incredibly thankful for.

    Posted by Susan Davis on June 4,2010 | 09:35 AM

    This truely makes one consider donating their body to science upon death.

    Posted by abayna4 on June 8,2010 | 03:30 PM

    Excellent!!! I will definitely share this story with my students and my children. I will get two copies of the book and donate one to my school's library and keep the other in my personal library. Thank you for your persevernce and committment. Excellent job! Blessings to the family of the late "GREAT Henrietta." :)

    Posted by JCoats on July 3,2010 | 06:53 PM

    I just finished reading this book - well written and quite a testimonial to Henrietta and her family. I am a supporter of research but have never really stopped to think about the emotional impact it has on the doner and their family members. How do we determine the rights of a cell? I believe informed consent is crucial - allow researchers to do what they need to do while ensuring that the doner/family wishes are followed.
    Thank you Henrietta for your unknowing contribution to science and health research - what an impact you have made -
    I am humbled by that! Not sure that any one else in the near future will impact mankind in the way you have.

    Posted by Laura Habel on July 7,2010 | 11:15 AM

    The cells were taken without her consent or knowledge. She could barely read and certainly couldn't understand cell culture. John Hopkins took advantage of her because she was poor, uneducated and a Black woman. Poor Blacks are always taken advantage of, that's why Black people distrust doctors and law enforcement...it's a healthy fear, for sure. Henrietta's family deserve compensation for their mothers, multi-million dollar cell contribution to science and medicine. That's just common sense. Of course, it's racist what John Hopkins and their doctors/scientists were doing to poor Blacks. How is it that this woman's cells made such a MAJOR impact on science and medicine and her immediate family at least has no health insurance. Come on now, it's the right thing to do to insure her family is taken care of. If the doctors, scientists, researchers profited from Henrietta Lacks' cells why shouldn't her family be compensated as well? And now this book has been written and the author will profit. I'm not saying she shouldn't get paid for her book, it's an awesomely informative story and I'm grateful she was compelled to tell it the way it actually happened, but everybody profits except the poor family. Some of you want to look at the family as if they're wrong for wanting to be compensated after all these others have made mega millions of their mother's cell culture. It was an enormous contribution to science and medicine, many people profited, they didn't share their findings for nothing. It's about advancing science and medicine AND getting paid, don't get it twisted!

    Posted by Reign on July 13,2010 | 08:18 AM

    This was a fascinating book about a courageous woman. I did a school research paper on Henrietta and the disgrace of medical aparteid.

    Posted by Andrea Keyes on July 17,2010 | 04:52 PM

    Just amazing! Will the family ever reap any benefits?

    Posted by Renalda Whitaker on August 26,2010 | 01:56 PM

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