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

    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

    Hey Singh, Go to Amazon.com and order the book,' The Immortal Life of Henrietta Lacks by Rebecca Skloot'. I hope this helps.

    Posted by Bruce on February 1,2010 | 03:46 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

    Fantastic story!! Fantastic article I've never really wanted to buy a book that had to do with science and cells before but can not WAIT to find out where I can get this book!!!! Fascinating!!!!!

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

    Amazing what those in power are able to do to the minority with impunity. I'm glad Ms. Larks is finally getting some recognition for her world changing contributions. I also hope Johns Hopkins finds a way to begin to repay her family for this tremendous contribution.

    Posted by L. Senior on February 1,2010 | 04:00 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

    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