The Immortal Life of Henrietta Lacks

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Rebecca Skloot: The Immortal Life of Henrietta Lacks (EBook, 2010, Crown Publishing Group)

Electronic resource

English language

Published Nov. 8, 2010 by Crown Publishing Group.

ISBN:
978-0-307-58938-5
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OCLC Number:
630604088

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3 stars (4 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 …

18 editions

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

2 stars

Of course it's heartbreaking that Henrietta Lacks's descendants must do without medical insurance while Henrietta's cells provide financial benefits to pharmaceutical companies. Rebecca Skloot concludes the book with a really good (if scholarly) analysis of the issues regarding tissue "donation" and medical research.

The story of the Lacks family was compelling; the historical record of the scientists and medical personnel was rather dry. In the end, I felt like there were too many competing storylines in this book to really make me feel involved with all of them.

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

2 stars

Of course it's heartbreaking that Henrietta Lacks's descendants must do without medical insurance while Henrietta's cells provide financial benefits to pharmaceutical companies. Rebecca Skloot concludes the book with a really good (if scholarly) analysis of the issues regarding tissue "donation" and medical research.

The story of the Lacks family was compelling; the historical record of the scientists and medical personnel was rather dry. In the end, I felt like there were too many competing storylines in this book to really make me feel involved with all of them.