The beginning of this book was interesting and kept me listening. I learned some interesting information about cell research. But sadly by the time I began listening to Part 2, my interest was waning. The trials and tribulations of the Lacks children (mainly as adults) took over the story and became tedious. I think Skloot became too involved with the family, thus losing her objectivity and was unable to write an unbiased story. I finished the book but was disappointed with the final 1/4 of the book.
The narrators did a fine job and their delivery helped me make it to the end of the book.
I am an avid eclectic reader.
This is a well-written non-fiction book, that provides back ground information about unfair treatment of minorities by medical research. Cassandra Campbell and Bahni Turpin did great job with the narration of the book. The story of Henrietta Lacks and her family is interesting and the discovery and care of the Hi La cells. One major item about the family is the lack of education played a major role in their understanding and ability to control the situation. The book accomplishes its goal of promoting proper documentation of biological tissue research. It raises the question of ownership of our own tissues and whether or not we have proprietary rights to our bodies in situ or in vitro. This question needs to be answered NOW not in the future. The other teaching of the book was how important education is to each individual. This is an absolute must read book for everyone on this planet.
I LOVE BOOKS! I have a service business (large salon). 'What are you reading' is heard all day everyday.
Exceptionally well wrought!! A history, biology and genealogical story cleverly wrapped in well narrated format. I truly enjoyed this listen and appreciated the author's painstaking patience with the Lacks family and the in-depth explanation of the HELA cell's science. It's hard to imagine a biology lesson being presented in any better arrangement. Thanks and BRAVO Rebecca!
This is a necessary book - aside from informing us about what seems today like the the dark ages of cancer research and the reported unfair treatment of minorities by the medical community in the era of Henrietta Lacks, it's time we all became more enlightened as to the fate of our body products once we part with them in a doctor's office, lab or hospital. This book raises important issues as to the space required for storage of all discarded tissue, which is unlike printed material that can be converted to digital format.
As an historical novel there are bound to be characters that are not "likable" nor relatable in the usual fictional sense. This family was troubled in many ways, in addition to the implied racial implications, the possible malpractice issues regarding the HeLa cells, and losing any financial stake in the success of the HeLa cell line. The family came to Baltimore to be part of the then growing steel industry. They were originally from a bare bones town in Virginia, having farmed their own tobacco crops after indirectly inheriting the property after being emancipated from slave status. There were some hard workers amongst the marginal characters, but basically this was a hard-strapping family who had to make do in order to survive. And several of them fell by the wayside to crime and mental dysfunction.
The book is well-written, even with the frequent disjunctions in time periods. It can be difficult to follow the genealogy and plethora of major and minor characters, and the myriad mentions of various studies. But all that is mere technicality.
The book accomplishes its goal of promoting proper documentation of, and credit for - financial or otherwise - biological tissues that are saved and used for research. It raise the question of ownership of our own tissues, and whether or not we have proprietary rights to our own bodies, in situ or in vitro.
Audible Member Since 2003
Rebecca Skloot spent ten years of her life researching and writing this book. At the time she had no way of knowing just what she was getting herself into.
The HeLa cell line is one of the most important and studied subjects in the world of medicine and biology, but practically nothing was known about the person from which these cells were named, Henrietta Lacks. In fact, for years even the name Henrietta Lacks was intentionally obscured by the fictitious names of Helen Lane or Helen Larson.
Skloot was a young student at the time she became interested in the mostly anonymous Henrietta Lacks, who died at the age of 31 from a terribly aggressive form of cervical cancer. Her cells were extracted, without permission or informed consent, becoming for all purposes the first line of "immortal" human cells living outside of the host body. The author decided to attempt to put a human face on the donor of the cells which played a vital part in such scientific advances as in the cure for polio, aids research, genetic discoveries, cancer cures, drug developments, to name just a few. However, learning the true story of the Lacks family two generations after the death of Henrietta turned out to be quite the daunting venture as Skloot tenaciously uncovers layers of family suffering, mistrust, ignorance and exploitation.
The Immortal Life of Henrietta Lacks is a real-life story of family and all that goes along with it, good and bad. It is in-part a tale of mystery that walks into real human drama, tackling many difficult issues of racism, bio-ethics, privacy and profiteering.
This book is perfectly narrated and is one of the best audio books I have encountered in quite some time. Do not miss this one!
A Heartbreaking story that details the illogical justification used by scientists and the market establishment they created to reason away that an individual's biological material is not their own or something they can uniquely own and patent or trademark but instead can only be patented and trademarked by a scientist or corporation (manufactured individual). This woman from America's racial and economic underclass's unique and special biological cells pioneered science and are now sold as the property of a corporation. She died in poverty and her progenitors and spouse struggled and suffered greatly as the medical and science establishment exploited their ignorance while making huge advancements and wealth with the immortal cells of this poor woman without even giving proper public credit or respect.
Gen-Xer, software engineer, and lifelong avid reader. Soft spots for sci-fi, fantasy, and history, but I'll read anything good.
The Immortal Life of Henrietta Lacks, like many compelling works of nonfiction, was written to tell one story, but, in its creation, uncovered several others. On the surface, Rebecca Skloot's book is about a line of cells, extracted from a single cancer patient in the 1950s, that went on to be the most widely studied human cell line in the world. On another level, it's about an evolving debate over the medical ethics of cell and DNA ownership. How much say should patients have in the use of their own genetic material? How does society balance the needs of medical research against concerns for privacy and individual autonomy?
On still another level, The Immortal Life of Henrietta Lacks is about race relations in America, about uneven levels of white privilege and black privilege when it comes to access to information and advocacy. It's a story about casual exploitation by a scientific establishment that was trained to compartmentalize and not think of its work in personal terms. Finally, it's a story of a family struggling to find emotional and spiritual closure after the years following the death of their mother, who continues in a strange and somewhat mystifying afterlife.
If the book had simply been about science and ethical questions pertaining to the cells of Henrietta Lacks, I might not have found it more than mildly interesting, but the human element gives the story many more dimensions. I think Skloot did an excellent and honest job of conveying how one poor, black family from the rural South perceives science and medicine. Of course, they understand and care about the basic things that most Americans do, but their views are colored by a history and identity that, I, a well-educated, middle-class white northerner, simply haven't lived in. It was a fascinating and ultimately hopeful exploration beyond stereotypes and into how human beings really relate to questions that can never be entirely viewed in clinical, medical terms. You get to know Henrietta's extended family, and to view her life and unintended contribution to science as they do.
Overall, the book felt like an extended episode of This American Life, in that it didn’t explore (or resolve) any issue in great depth, but was engagingly put together and taught me a little about a lot of different subjects. Since it’s not a long read, I’d say it’s well-deserving of its awards and your time.
This book is interesting, well written, and important. I learned so much about the science of cells, as well as the human side of this kind of research.
I hear voices. But maybe that's because there's always an Audible book in my ear.
This meticulously researched and written book is at the top of the heap. The writing, through spare, is perfect for the subject. The narration is spot-on. Where some non-fiction can lag, the author did an incredible job of actually bringing the story along. No matter what you think about medical research or bio-ethics, this book will make you rethink your stand. If you don't care about those issues, reading about Henrietta Lacks alone is worth the time. Simply brilliant in every possible way.