- Paperback: 400 pages
- Publisher: Broadway Books; Media Tie In edition (April 4, 2017)
- Language: English
- ISBN-10: 0804190100
- ISBN-13: 978-0804190107
- Product Dimensions: 5.2 x 0.9 x 8 inches
- Shipping Weight: 10.6 ounces (View shipping rates and policies)
- Average Customer Review: 5,836 customer reviews
- Amazon Best Sellers Rank: #51,016 in Books (See Top 100 in Books)
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The Immortal Life of Henrietta Lacks (Movie Tie-In Edition) Media Tie In Edition
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"One of the most graceful and moving nonfiction books I’ve read in a very long time…'The Immortal Life of Henrietta Lacks'…floods over you like a narrative dam break, as if someone had managed to distill and purify the more addictive qualities of 'Erin Brockovich,' 'Midnight in the Garden of Good and Evil' and 'The Andromeda Strain.'…it feels like the book Ms. Skloot was born to write. It signals the arrival of a raw but quite real talent.”—Dwight Garner, The New York Times
"Skloot's vivid account begins with the life of Henrietta Lacks, who comes fully alive on the page…'Immortal Life' reads like a novel."--Eric Roston, The Washington Post
“Gripping…by turns heartbreaking, funny and unsettling…raises troubling questions about the way Mrs. Lacks and her family were treated by researchers and about whether patients should control or have financial claims on tissue removed from their bodies.”—Denise Grady, New York Times
“The Immortal Life of Henrietta Lacks’’ is a fascinating read and a ringing success. It is a well-written, carefully-researched, complex saga of medical research, bioethics, and race in America. Above all it is a human story of redemption for a family, torn by loss, and for a writer with a vision that would not let go.”—Douglas Whynott, The Boston Globe
"Riveting...raises important questions about medical ethics...It's an amazing story...Deeply chilling... Whether those uncountable HeLa cells are a miracle or a violation, Skloot tells their fascinating story at last with skill, insight and compassion" —Colette Bancroft, St. Petersburg Times
“The history of HeLa is a rare and powerful combination of race, class, gender, medicine, bioethics, and intellectual property; far more rare is the writer than can so clearly fuse those disparate threads into a personal story so rich and compelling. Rebecca Skloot has crafted a unique piece of science journalism that is impossible to put down—or to forget.”—Seed magazine
“No one can say exactly where Henrietta Lacks is buried: during the many years Rebecca Skloot spent working on this book, even Lacks’s hometown of Clover, Virginia, disappeared. But that did not stop Skloot in her quest to exhume, and resurrect, the story of her heroine and her family. What this important, invigorating book lays bare is how easily science can do wrong, especially to the poor. The issues evoked here are giant: who owns our bodies, the use and misuse of medical authority, the unhealed wounds of slavery ... and Skloot, with clarity and compassion, helps us take the long view. This is exactly the sort of story that books were made to tell—thorough, detailed, quietly passionate, and full of revelation.”—TED CONOVER, author of Newjack and The Routes of Man
“It’s extremely rare when a reporter’s passion finds its match in a story. Rarer still when the people in that story courageously join that reporter in the search for what we most need to know about ourselves. When this occurs with a moral journalist who is also a true writer, a human being with a heart capable of holding all of life’s damage and joy, the stars have aligned. This is an extraordinary gift of a book, beautiful and devastating—a work of outstanding literary reportage. Read it! It’s the best you will find in many many years.”—ADRIAN NICOLE LEBLANC, author of Random Family
”The Immortal Life of Henrietta Lacks brings to mind the work of Philip K. Dick and Edgar Allan Poe. But this tale is true. Rebecca Skloot explores the racism and greed, the idealism and faith in science that helped to save thousands of lives but nearly destroyed a family. This is an extraordinary book, haunting and beautifully told.”—ERIC SCHLOSSER, author of Fast Food Nation
“Skloot’s book is wonderful -- deeply felt, gracefully written, sharply reported. It is a story about science but, much more, about life.”—SUSAN ORLEAN, author of The Orchid Thief
“This is a science biography like the world has never seen. What if one of the great American women of modern science and medicine--whose contribution underlay historic discoveries in genetics, the treatment and prevention of disease, reproduction, and the unraveling of the human genome--was a self-effacing African-American tobacco farmer from the Deep South? A devoted mother of five who was escorted briskly to the Jim Crow section of Johns Hopkins for her cancer treatments? What if the untold millions of scientists, doctors, and patients enriched and healed by her gift never, to this day, knew her name? What if her contribution was made without her knowledge or permission? Ladies and gentlemen, meet Henrietta Lacks. Chances are, at the level of your DNA, your inoculations, your physical health and microscopic well-being, you’ve already been introduced.”--MELISSA FAY GREENE, author of Praying for Sheetrock and There Is No Me Without You
“Heartbreaking and powerful, unsettling yet compelling, The Immortal Life of Henrietta Lacks is a richly textured story of the hidden costs of scientific progress. Deftly weaving together history, journalism and biography, Rebecca Skloot?s sensitive account tells of the enduring, deeply personal sacrifice of this African American woman and her family and, at long last, restores a human face to the cell line that propelled 20th century biomedicine. A stunning illustration of how race, gender and disease intersect to produce a unique form of social vulnerability, this is a poignant, necessary and brilliant book.”—ALONDRA NELSON, Columbia University; editor of Technicolor: Race, Technology and Everyday Life
“Rebecca Skloot has written a marvelous book so original that it defies easy description. She traces the surreal journey that a tiny patch of cells belonging to Henrietta Lacks’s body took to the forefront of science. At the same time, she tells the story of Lacks and her family—wrestling the storms of the late twentieth century in America—with rich detail, wit, and humanity. The more we read, the more we realize that these are not two separate stories, but one tapestry. It’s part The Wire, part The Lives of the Cell, and all fascinating.”—CARL ZIMMER, author of Microcosm
“If virtues could be cultured like cells, Rebecca Skloot’s would be a fine place to start¾a rare combination of compassion, courage, wisdom, and intelligence. This book is extraordinary. As a writer and a human being, Skloot stands way, way out there ahead of the pack.”—MARY ROACH, author of Stiff and Bonk
“The Immortal Life of Henrietta Lacks takes the reader on a remarkable journey—compassionate, troubling, funny, smart—and irresistible. Along the way, Rebecca Skloot will change the way you see medical science and lead you to wonder who we should value more—the researcher or the research subject? Ethically fascinating and completely engaging—I couldn’t recommend it more.”—DEBORAH BLUM, author of The Poisoner’s Handbook and The Monkey Wars and the Helen Firstbrook Franklin professor of journalism at the University of Wisconsin-Madison
“This remarkable story of how the cervical cells of the late Henrietta Lacks, a poor black woman, enabled subsequent discoveries from the polio vaccine to in vitro fertilization is extraordinary in itself; the added portrayal of Lacks's full life makes the story come alive with her humanity and the palpable relationship between race, science, and exploitation.—PAULA J. GIDDINGS, author of Ida, A Sword Among Lions; Elizabeth A. Woodson 1922 Professor, Afro-American Studies, Smith College
“Rebecca Skloot’s steadfast commitment to illuminating the life and contribution of Henrietta Lacks, one of the many vulnerable subjects used for scientific advancement, and the subsequent impact on her family is a testament to the power of solid investigative journalism. Her deeply compelling account of one family’s long and troubled relationship with America’s vast medical-industrial complex is sure to become a cherished classic.”—ALLEN M. HORNBLUM, author of Acres of Skin and Sentenced to Science
“Writing with a novelist’s artistry, a biologist’s expertise, and the zeal of an investigative reporter, Skloot tells a truly astonishing story of racism and poverty, science and conscience, spirituality and family driven by a galvanizing inquiry into the sanctity of the body and the very nature of the life force.”—BOOKLIST (starred review)
“Science journalist Skloot makes a remarkable debut with this multilayered story about ‘faith, science, journalism, and grace.’…Recalls Adrian Nicole LeBlanc’s Random Family…A rich, resonant tale of modern science, the wonders it can perform and how easily it can exploit society’s most vulnerable people.”—PUBLISHERS WEEKLY (starred review)
About the Author
Rebecca Skloot is an award-winning science writer whose work has appeared in The New York Times Magazine; O, The Oprah Magazine; Discover; and many others. She is coeditor of The Best American Science Writing 2011 and has worked as a correspondent for NPR’s Radiolab and PBS’s Nova ScienceNOW. She was named one of five surprising leaders of 2010 by the Washington Post. Skloot's debut book, The Immortal Life of Henrietta Lacks, took more than a decade to research and write, and instantly became a New York Times bestseller. It was chosen as a best book of 2010 by more than sixty media outlets, including Entertainment Weekly, People, and the New York Times. It is being translated into more than twenty-five languages, adapted into a young reader edition, and being made into an HBO film produced by Oprah Winfrey and Alan Ball. Skloot is the founder and president of The Henrietta Lacks Foundation. She has a B.S. in biological sciences and an MFA in creative nonfiction. She has taught creative writing and science journalism at the University of Memphis, the University of Pittsburgh, and New York University. She lives in Chicago. For more information, visit her website at RebeccaSkloot.com, where you’ll find links to follow her on Twitter and Facebook.
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It still amazes me that this is a woman's real life story, the story of her family, and how they have impacted science and anyone who works or benefits from the use of cellular research. That means just about every single person is connected to Henrietta in one way or another.
This was a great book that I'm so glad I read. I learned a lot and it kept me entertained and fascinated for days. It will really change your perspective and make you appreciate this woman's contribution to our scientific and health fields.
In “The Immortal Life of Henrietta Lacks,” Rebecca Skloot introduces us to the “real live woman,” the children who survived her, and the interplay of race, poverty, science and one of the most important medical discoveries of the last 100 years. Skloot narrates the science lucidly, tracks the racial politics of medicine thoughtfully and tells the Lacks family’s often painful history with grace. She also confronts the spookiness of the cells themselves, intrepidly crossing into the spiritual plane on which the family has come to understand their mother’s continued presence in the world. Science writing is often just about “the facts.” Skloot’s book, her first, is far deeper, braver and more wonderful.
This work has the most human of stories at its core, and never deviates from that important, and often heartbreaking, humanity. When science appears, it does so effortlessly, with explanations of cell anatomy or techniques like “fluorescence in situ hybridization” seamlessly worked into descriptions of the coloured wards of Johns Hopkins hospital to Lacks’s hometown of Clover, Virginia.
But The Immortal Life of Henrietta Lacks is not a comfortable read. I visibly winced at descriptions of Henrietta’s blackened, burned skin after multiple rounds of devastating radiation treatments. I put the book down with a heavy sigh after reading about the experiments that black Americans have been unwittingly subjected to over the years. I cried twice, at events that I can’t talk about without seriously spoiling the book. But it is uplifting too, particularly in a stand-out chapter where Henrietta’s children, Deborah and Zakariyya, visit a cancer researcher to see their mother’s cells under a microscope.
All of this is to be expected of a book that refuses to shy away from tackling important themes – the interplay between science and ethics, the question of who owns our bodies, and the history of racism in the US. And yet for all its grand scope, skilful writing and touching compassion, there is one simple element that makes As a final thought, I was struck by the parallels between Henrietta’s cells and her story. Henrietta’s entire family history was eventually condensed into a small sliver of cells that you could carry in a glass vial. They have achieved immortality, used by scientists throughout the world. Similarly, her entire life has been condensed into a moving tale and an exceptional book that you could read in a comfortable day. By right, it will achieve the same immortal status.
But it's more than that, it's the story of Henrietta's family finding out 20 years later that their mother's cells are alive, and helping medical science! They deal with anger, disbelief, and a feeling of betrayal, since others have made money from her Henrietta's cells and they, ironically, can't afford health insurance! Skloot does a wonderful job describing the ongoing difficulties meeting the family and gaining their trust, describing their emotions and reactions (including superstition) in a way that humanized them. Many books have been written about the HeLa (HEnrietta LAcks) cells and the their effect on medical science. This book tells you what kind of person she was, and how it affected her family. One of the best books I've read in a while.
The book is really several parallel stories tied closely together. First, there's Henrietta Lack's own story and those of the HeLa cell line developed from her biopsy tissues in 1951. Then there is the story of the Lacks family; impoverished, poorly educated, and ignorant of their mother's medical signifiance. Finally, there's the author's own story about her multi-year effort of research, interviews, and writing Henrietta Lacks' story. At times, the intertwined stories seemed to get in each others way. The disappointing thing to me, is that Henrietta's story itself, gets rather short shrift while the peripheral stories of Henrietta's children, grandchildren, etc.; as well as the author's story, take up the lion's share of the book.
These are fairly minor complaints, however. The book is unique, interesting, and most importantly, a joy to read and I recommend it.