The Immortal Life of Henrietta Lacks

Very informative and very easy to read.

Unfortunately many Native Americans endured worse experiments on their bodies and no one writes about them. Hopefully Henriett's children will win their law suit against all the labs that have made billions off her cells since 1953 and still are.

There's a lot to experience in this book. Infuriating abuse of patients, children trying to make sense of the loss of their mother, and the amazing way tissue samples can be used to advance medical science. We all stand to gain from tissue collection but what are we willing to give up? Where do we draw the line on privacy and human rights? Who is making money from the sale of your child's tonsillectomy? Was that recent blood test really necessary? What about that DNA test you took to "discover" your ancestry?

Sensitive look into the negative effects of the medical community taking advantage of a poor, uneducated, ill woman. Interesting and easy to understand explanations of cells and cell lines.

This is one of the most even handed reveiws of this topic I've read. Ms. Skloot's style is in the best narrative tradition. I literally hated to put the book down. It provides good insights into the poor relations that the biomedical industry has particularly with the African-American community and the tragedy that a loose attitude toward patient confidentiality and wishes can have. Yet her book is very even handed in discussing the damage that would occur if subject rights were asserted to the maximum. I take from this that it is high time that the research community address this in a proactive manner and develop a binding policy and statutory framework that makes clear the ground rules. I thank her for sharing such a powerful and touching story with all of us. Dr. Timothy Drevyanko, MD, MS

Equal parts history, psychological drama, expose and character study, Rebecca Skloot's gripping debut is a deeply affecting tour de force that effortlessly bridges the gap between science and the mainstream. Her subject is the multilayered drama behind one of the most important--and in many ways, problematic--advances of modern medicine. Captivated by the story of Henrietta Lacks, a poor African-American woman whose cervical cancer cells (dubbed HeLa) were the first immortalized cells grown in culture and became ubiquitous in laboratories around the world, Skloot set out to learn more about the person whose unwitting "donation" of the cells transformed biomedical research in the last century. Her research ultimately spanned a decade and found her navigating (and to some extent, mediating) more than 50 years of rage over the white scientific establishment's cavalier mistreatment and exploitation of the poor, especially African Americans. Skloot deftly weaves together an account of Lacks's short life (she died at age 31) and torturous death from an extremely aggressive form of cancer; the parallel narrative concerning her cells; and the sometimes harrowing, sometimes amusing chronicle of Skloots's own interactions with Lacks's surviving (and initially hostile and uncooperative) family members. Moving comfortably back and forth in time, the richly textured story that emerges brings into stark relief the human cost of scientific progress and leaves the reader grappling with many unanswered questions about the ethics of the scientific endeavor, past and present. While the goals of biomedical research may be noble, how they are achieved is not always honorable, particularly where commercialization of new technologies is at stake. Skloot offers a clear-eyed perspective, highlighting the brutal irony of a family whose matriarch was a pivotal figure in everything from the development of Jonas Salk's polio vaccine to AIDS research to cancer drugs, yet cannot afford the very medical care their mother's cells helped facilitate, with predictable consequences. The LA Times book review section named Skloot one of its four "Faces to Watch in 2010," an honor that, based on "The Immortal Life of Henrietta Lacks" is well-deserved. Five stars--it was hard to put down this compelling, admirable and eminently readable book.

As I recall this book was categorized as CANCER, I believe it might be more aptly described as science based non-fiction. In the last two decades I've seen occasional news items alluding to human cells taken from a black woman in the 1950's that have been replicated millions of times. The cells are referred to as HeLa and on the face of it I wouldn't have thought there was much of a story behind the extraction of these cells and their use by the biomed industry. However, this book dispells that rather naive assumption completely and puts a name and a face, a family, and a story behind the contents of many petri dishes and slides. THE IMMORTAL LIFE OF HENRIETTA LACKS explains how the cells were obtained, replicated, distributed, and used without informed consent of the owner and family by John Hopkins and how they benefitted mankind w/o compensation to the family. Author Skloot tells the story of a family victimized by socioeconomic conditions and racism that can't get fundamental things like health coverage while these cells make a lot of money for the health establishment. It is a disturbing read that will stay with the reader long after the book is finished. It may also make the reader take a long hard look at the need for standardized health care in our society among many other things. The one thing that I found fascinating about this book is how Skloot managed to take a generally dry topic that might have been addressed in a scientific textbook and humanized it on a very personal level by developing a close relationship with Henrietta's family. The input received from the family took this book to a higher level and made it a very personsl story. From my perspective, it was very hard not to get involved with the Lacks family and not feel their sense of betrayal and loss.