The Immortal Life of Henrietta Lacks

paperback, 384 pages

Published Jan. 1, 2011 by Pan Publishing, PAN.

ISBN:
978-0-330-53344-7
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4 stars (14 reviews)

Her name was Henrietta Lacks, but scientists know her as HeLa. She was a poor black tobacco farmer whose cells—taken without her knowledge in 1951—became one of the most important tools in medicine, vital for developing the polio vaccine, cloning, gene mapping, in vitro fertilization, and more. Henrietta’s cells have been bought and sold by the billions, yet she remains virtually unknown, and her family can’t afford health insurance.

This New York Times bestseller takes readers on an extraordinary journey, from the “colored” ward of Johns Hopkins Hospital in the 1950s to stark white laboratories with freezers filled with HeLa cells, from Henrietta’s small, dying hometown of Clover, Virginia, to East Baltimore today, where her children and grandchildren live and struggle with the legacy of her cells. The Immortal Life of Henrietta Lacks tells a riveting story of the collision between ethics, race, and medicine; of scientific discovery and faith …

14 editions

More about the author and the process than the HeLa cells

2 stars

I picked up this book hoping it would tell me more about the HeLa cells and the background to them. It sort of does that, except it's really more a book about how the author gathered the information in the book - "I went here, met X, went somewhere else, met Y". As a result, it ends up feeling like the author has inserted herself into the story, and perhaps also got a bit too close to the participants.

For me, this is one of those books which isn't that fulfilling on its own, but a good jumping off point by following up the references etc.

Review of 'The Immortal life of Henrietta Lacks' on 'Goodreads'

4 stars

Anyone who is interested in medical history or medicine has probably heard of the immortal HeLa cells.

Now here is your chance to find out the real story behind the woman who “donated” her cells.

For those of you who know what happened, you know that Henrietta didn’t donate her cells. She wasn’t even asked. The cells were just taken because that’s what was done to poor black patients back in the segregated days.

While I knew the basic story (and her real name), I wasn’t as familiar with her as person, the exact circumstances of her disease and the cells named after her. This was the author’s obsession: to find out as much as she could about Henrietta and the circumstances of her cells.

While this was a very well written book, I didn’t enjoy it as much as other medical history books, but I would put it on …

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