The Immortal Life of Henrietta Lacks

The Immortal Life of Henrietta Lacks

Audiobook CD - 2010
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Documents the story of how scientists took cells from an unsuspecting descendant of freed slaves and created a human cell line that has been kept alive indefinitely, enabling discoveries in such areas as cancer research, in vitro fertilization, and gene mapping.
Publisher: New York : Random House Audio, p2010
ISBN: 9780451486318
Branch Call Number: 616.0277
Description: 10 sound discs (12 1/2 hr.) : digital ; 4 3/4 in
Additional Contributors: Campbell, Cassandra


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IndyPL_SteveB Nov 30, 2018

An excellent audio book of this fascinating true story.

In 1951, Henrietta Lacks, a poor African American mother from Virginia, died of cervical cancer. An unremarkable occurrence, perhaps, except that before her death, doctors took samples of her tumor and made them the first successful culture of human cells, a line of cells now known as HeLa. Her cells have continued to reproduce ever since, in the number of uncounted billions, in research labs all over the world. The research done on these cells have saved millions of lives – yet her family did not find out about these cells for 20 years and never received a dollar of compensation.

In a remarkably moving account, the author contrasts the amazing success of the HeLa cells with the decades-long agony of the Lacks family. The author forces us to ask uncomfortable questions about the nature of medical research and who owns our cells and DNA. But she also explores the very human story of an impoverished, uneducated family thrust into the limelight, not knowing whom to trust. The author became an unofficial member of the Lacks family in the years she spent developing this story. Winner of several awards as best science or medical book of the year and an amazing combination of science and personal history.

Oct 27, 2017

You may have heard of HeLa cells, cells that have been tested & researched leading to about every medical advancement achieved since 1951! Those cells were part of a living, breathing lady named Henrietta Lacks (“He - Henrietta , “La” - Lacks). Upon hearing Lacks’ name in her college science class, she wanted more details of the person that “donated” the cells that have revolutionized genetic science as we know it. Nobody really knew much about her. This led her on a quest to get to know Henrietta & give her the credit & honor she is due. She is joined in her quest by Henrietta’s only surviving daughter, Deborah “Dale”. Together they uncover the truth behind Deborah’s mother’s & sister Elsie’s life & death. This journey opened up questions & turmoil that Deborah didn’t have before this point. Ultimately Deborah, her brothers, & Henrietta’s extended family found peace in knowing the truth & bringing honor to their mother’s contribution to the world of science.

I had heard of HeLa cells before discovering this book, but I too had never thought about the life behind these cells. The background behind Henrietta’s illness, her “donation” of cells, & the following genetic & medical discoveries was absolutely fascinating! I liked how the author told the personal & scientific stories simultaneously by switching back & forth to create a greater understanding & personal attachment to both. I loved the bond that Skloot (author) & Deborah built from the the first phone call to Deborah’s final breath. No person is beyond warmth, caring, & friendship.

Age recommendation: 14 & up (some profanity, lots of scientific research, proper medical terminology for reproductive organs)

On a scale of 1-10 stars, I give it 8.

JCLJoyceM Mar 20, 2017

You have to admire the author’s pursuit of this story in spite of the many times that Henrietta’s family waffled in their cooperation. Given the family’s treatment by hospitals, it is entirely understandable that they would hesitate. They became aware of the extraordinary ways the cells were being used for medical research, but could barely afford to see a doctor themselves.
I listened to the audio version. If I’d had the print version, I probably would have skipped some of the chapters related to the science details.

Andover1 Sep 10, 2015

Wanted to listend to this book, DID NOT enjoy the experience. This is a great book, read it instead!

bbonier Jan 19, 2013

Henrietta Lacks was a poor black woman who died of cervical cancer at the age of 30, leaving behind 5 small children. She was treated at Johns Hopkins Hospital in Baltimore and her doctor took samples of her cervical cells, both normal and cancerous, to use for his tissue research. All the other cells that he had tried to keep alive died. But Henrietta's continued to reproduce at an alarming rate. Thus was born the HeLa cell. The doctor distributed the cells for research to other scientists and the cells became an important tool in developing the polio vaccine. They were also used in uncovering secrets of cancer, viruses and the atom bomb's effects, leading to important medical advances that have saved many lives. All the while the Lacks family was kept in the dark and did not receive any compensation. Very well read by Cassandra Campbell with Bahni Turpin.

Aug 26, 2012

The Immortal Life of Henrietta Lacks raises all sorts of ticklish issues, and is an important read for anyone who wants to understand the possible ramifications, both positive and negative, of ever-advancing technology in the research and medical communities. Some have criticized the author's approach, suggesting there's just too much of Skloot herself in the book. I felt that at times while reading the book, but overall believe that Skloot's interaction with the Lacks family and the personal relationship she established with them did more to enhance than to harm the telling of this story. Apart from her relationship with the Lackses, I doubt Skloot would have been able to bring the person of Henrietta to life as she did. I wish there were clear answers to the issues raised by The Immortal Life of Henrietta Lacks, but at least Skloot has gotten the questions on the table.

Aug 19, 2012

This is a work of non-fiction but told as a narrative. It is formatted so you get a mixture of anecdotal story and documentary facts; all interwoven to create a compelling read. The subject matter is primarily about the lack of formal consent needed by doctors to harvest anyone’s cells or tissues during common medical examinations and the total absence of regulation by researchers /scientists to use this biological material in an endless variety of tests, trials, and purposes. The narrative is about the huge impact this has on a poor black family, when the truth surfaces about a deceased family member whose super viable cells have been harvested and used extensively for many years in innumerable ways, from testing how human cells react to nuclear radiation to sending them into space, to playing an important part in finding vaccines and cancer treatments.
This book raises quite a few controversial questions like should people be told if their cells are being harvested? Should patients have the right to determine how and to what purpose their cells are being used and should they be able to share in the profits of big pharmaceutical companies seeing as they were a major contributor to their discoveries? Would doing so impede the progress of science? This was an eye-opener for me and a thoroughly enlightening experience. If this sounds like a real x- file episode, it is because it is one. This is a subject everyone needs to be aware of.

Jan 07, 2011

Boy, did Skloot get the story of a lifetime here. I think others might have written it better, but kudos to her for pursuing it. It's absolutely mindblowing that a huge portion (majority?) of medical research has been performed on the cell tissue of one woman, a young black mother who died at 31--and that her children never knew that modern medicine was built upon their mother's back.


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Oct 27, 2017

jandt_mcmurray thinks this title is suitable for 14 years and over


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