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The Immortal Life of Henrietta Lacks de…
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The Immortal Life of Henrietta Lacks (edição: 2010)

de Rebecca Skloot

MembrosResenhasPopularidadeAvaliação médiaConversas / Menções
11,523688421 (4.15)2 / 830
Her name was Henrietta Lacks, but scientists know her as HeLa. She was a poor Southern tobacco farmer, yet her cells--taken without her knowledge--became one of the most important tools in medicine. The first "immortal" human cells grown in culture, they are still alive today, though she has been dead for more than sixty years. HeLa cells were vital for developing the polio vaccine; uncovered secrets of cancer and viruses; helped lead to in vitro fertilization, cloning, and gene mapping; and have been bought and sold by the billions. Yet Henrietta Lacks is buried in an unmarked grave. Her family did not learn of her "immortality" until more than twenty years after her death, when scientists began using her husband and children in research without informed consent. The story of the Lacks family is inextricably connected to the dark history of experimentation on African Americans, the birth of bioethics, and the legal battles over whether we control the stuff we are made of.… (mais)
Membro:materbach
Título:The Immortal Life of Henrietta Lacks
Autores:Rebecca Skloot
Informação:Crown (2010), Edition: First Edition, Hardcover, 384 pages
Coleções:Sua biblioteca
Avaliação:
Etiquetas:Nonfiction, science

Detalhes da Obra

The Immortal Life of Henrietta Lacks de Rebecca Skloot

Adicionado recentemente porandrisll, biblioteca privada, MamaJ2016, LuannNelson, harray, ejmw, carol.valentine, tmullis, andrew.johnson2
  1. 140
    The Spirit Catches You and You Fall Down de Anne Fadiman (kidzdoc)
  2. 50
    Medical Apartheid: The Dark History of Medical Experimentation on Black Americans from Colonial Times to the Present de Harriet A. Washington (lives4laughs, fannyprice)
  3. 50
    The Warmth of Other Suns: The Epic Story of America's Great Migration de Isabel Wilkerson (bunnygirl)
    bunnygirl: personal history and stories linked with the larger African American history. if you were wondering about Skloot's reference to the Lacks family being part of the Great Migration, this book explains exactly what it is and tells the stories of three families in a similar manner.… (mais)
  4. 73
    Stiff: The Curious Lives of Human Cadavers de Mary Roach (VenusofUrbino)
    VenusofUrbino: If you like well-researched and well-written non-fiction like "Immortal Life" then you will also appreciate Mary Roach.
  5. 40
    A Lesson Before Dying de Ernest J. Gaines (krazy4katz)
    krazy4katz: Reading "The Immortal Life of Henrietta Lacks," I was pained by the impoverished lives of people who still lived on plantations in the 1940s - lack of schooling, lack of health care, lack of any kind of decent housing etc. "A Lesson Before Dying" more directly addresses the life of people still living on plantations in the '40s. Even though I sort of knew this, it was an emotional shock to truly recognize that all the abuse and oppression did not end with the Civil War but was still there 80 years later.… (mais)
  6. 30
    Body Hunters: How the Drug Industry Tests Its Products On the World's Poorest Patients de Sonia Shah (legxleg)
  7. 41
    Better: A Surgeon's Notes on Performance de Atul Gawande (Othemts)
  8. 20
    The Plutonium Files: America's Secret Medical Experiments in the Cold War de Eileen Welsome (barbharris1)
  9. 20
    Rosalind Franklin: The Dark Lady of DNA de Brenda Maddox (beyondthefourthwall)
  10. 20
    The Mapmaker's Wife: A True Tale of Love, Murder, and Survival in the Amazon de Robert Whitaker (sboyte)
    sboyte: Fascinating stories of the people behind great scientific discoveries.
  11. 10
    The Great Influenza: The Story of the Deadliest Pandemic in History de John M. Barry (LKAYC)
  12. 10
    The Forever Fix: Gene Therapy and the Boy Who Saved It de Ricki Lewis (krazy4katz)
    krazy4katz: Both of these books capture and humanize the process of medical discovery and the experiences of the patients. Although the authors have somewhat different backgrounds — Rebecca Skloot is a journalist with an undergraduate degree in biology, whereas Rikki Lewis has a PhD in genetics — I think the discussion of the scientific issues and the ethical issues regarding informed consent would appeal to the same readers.… (mais)
  13. 10
    Truevine de Beth Macy (akblanchard)
    akblanchard: Unusual medical conditions and racism as experienced by African Americans in the Jim Crow South.
  14. 10
    The Mockingbird Next Door: Life with Harper Lee de Marja Mills (akblanchard)
    akblanchard: In both books, journalists get personally involved with their subjects.
  15. 21
    The Wandering Gene and the Indian Princess de Jeff Wheelwright (LeesyLou)
    LeesyLou: If you have an interest in the social and personal ethics and background of medical care, this adds to your understanding. Minority cultures and personal medical ethics are equally poorly understood by many practitioners.
  16. 10
    The Juggler's Children: A Journey into Family, Legend and the Genes that Bind Us de Carolyn Abraham (sboyte)
  17. 10
    Life Itself: Exploring the Realm of the Living Cell de Boyce Rensberger (BookshelfMonstrosity)
    BookshelfMonstrosity: Cell cultures are being used to study diseases as well as cure them. Learn about the cell cultures called 'HeLa' in The Immortal Life of Henrietta Lacks, and read about cell cultures' utility as a whole in Life Itself.
  18. 12
    The Adoration of Jenna Fox de Mary E. Pearson (macart3)
    macart3: Deals with bioethics and human experimentation without others' consent.
  19. 12
    Tissue and cell donation : an essential guide de Ruth M. Warwick (Limelite)
    Limelite: Scientific discussion of medical/ethical, and other considerations regarding patients' rights and the medical profession's responsibilities on the subject, as well as other pertinent procedures.
  20. 04
    The Dangerous Joy of Dr. Sex and Other True Stories de Pagan Kennedy (Othemts)

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Mostrando 1-5 de 686 (seguinte | mostrar todas)
EVERYBODY should read this. It is the story of medical history, a treatise on medical ethics, the story of a search for answers by a writer and the history of a family.

There are many answers here. And it is a great beginning to a necessary conversation. ( )
  KittyCunningham | Apr 26, 2021 |
A fascinating insight into both the life of Henrietta Lacks and her HeLa cells which have contributed so much to modern medicine. ( )
  Aetherson | Apr 26, 2021 |
I've decided not to torture myself any longer, so I'm not finishing this book. I feel deceived, I delved into The Night Circus fully prepared to be amazed. There just isn't enough action to push this story along. The idea is intriguing, with tons of potential, but it gets lost in the frantic setting changes and perpetual descriptions. Yawn. ( )
  mbellucci | Apr 10, 2021 |
Fascinating. ( )
  mbellucci | Apr 10, 2021 |
I'm of two minds about this book. On the one hand, I enjoyed the scientific side of the story: the horror that was scientific research in the 1950s and the decades before informed consent became common practice; the discussion about cells and the research that can be conducted with them; and the legal and ethical ramifications of scientific research. In our world of HIPAA and institutional review boards, the information given in this book was both mind-opening and mind-blowing.

I did not enjoy what I felt was emotional manipulation on the part of the author. Look at these people and their horrible lives! Feel sorry for how poorly treated they've been! Their mother's cells have been used for research for years, yet they have no health insurance!

To be clear, I'm NOT a cold-hearted person. I believe everyone should have healthcare, regardless of their ability to pay for it. But this book wasn't about the state of the American health care system, as such. Nor was it, I'm sure, meant to be commentary on class or race issues in America. Yet those things were brought into the book, and I felt that they detracted from the real story, which was these amazing cells that survive and proliferate. Of course, that story by itself would have yielded a much shorter book, and perhaps a story that's already been told.

I didn't get the sense, despite what the author may have wished, that Henrietta was treated that much differently than any other woman with "female troubles" would have been in 1951. Surely, the segregation of Blacks and the complete lack of privacy given them in the hospital was deplorable, but I don't know that she would have gotten a different medical treatment - radiation, etc. - had she been a white woman with the same disease. I think her complaints would have been written off by the male doctors no matter who she was.

In book group, I posed the question of whether Henrietta's children would have turned out much differently had she lived, and the consensus was that the youngest would have had a much different life, a more secure, less anger-filled existence. But I don't know if it would have changed the overall outlook for the family.

I also felt that the author put herself into the story way too much, insinuating herself with the family when they were resistant to it -- continually resistant to it. There was no reporterly detachment here.

The medical and scientific aspect of this book is fascinating for anyone who is interested in such things; the family stuff detracts from the rest.

I would like to thank my book group for helping me solidify my thoughts on this book. ( )
  ssperson | Apr 4, 2021 |
Mostrando 1-5 de 686 (seguinte | mostrar todas)
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.
 
I put down Rebecca Skloot’s first book, “The Immortal Life of Henrietta Lacks,” more than once. Ten times, probably. Once to poke the fire. Once to silence a pinging BlackBerry. And eight times to chase my wife and assorted visitors around the house, to tell them I was holding one of the most graceful and moving nonfiction books I’ve read in a very long time.
adicionado por jlelliott | editarThe New York Times, Dwight Garner (Feb 2, 2010)
 
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, all driven by a galvanizing inquiry into the sanctity of the body and the very nature of the life force.
adicionado por sduff222 | editarBooklist, Donna Seaman (Dec 1, 2009)
 
Henrietta Lacks died of cervical cancer in a “colored” hospital ward in Baltimore in 1951. She would have gone forever unnoticed by the outside world if not for the dime-sized slice of her tumor sent to a lab for research eight months earlier. ...
Skloot, a science writer, has been fascinated with Lacks since she first took a biology class at age 16. As she went on to earn a degree in the subject, she yearned to know more about the woman, anonymous for years, who was responsible for those ubiquitous cells....
 
Skloot tells a rich, resonant tale of modern science, the wonders it can perform and how easily it can exploit society's most vulnerable people.
adicionado por Shortride | editarPublishers Weekly
 

» Adicionar outros autores (9 possíveis)

Nome do autorFunçãoTipo de autorObra?Status
Rebecca Sklootautor principaltodas as ediçõescalculado
Campbell, CassandraNarradorautor principalalgumas ediçõesconfirmado
Turpin, BahniNarradorautor principalalgumas ediçõesconfirmado
Acedo, Sara R.Designer da capaautor secundárioalgumas ediçõesconfirmado
Grip, GöranTradutorautor secundárioalgumas ediçõesconfirmado
Townsend, MandaFotógrafoautor secundárioalgumas ediçõesconfirmado

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For my family:

My parents, Betsy and Floyd; their spouses, Terry and Beverly;
my brother and sister-in-law, Matt and Renee;
and my wonderful nephews, Nick and Justin.
They all did without me for far too long because of this book,
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On January 29, 1951, David Lacks sat behind the wheel of his old Buick, watching the rain fall.
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...But I always have thought it was strange, if our mother cells done so much for medicine, how come her family can't afford to see no doctors? Don't make no sense. People got rich off my mother without us even knowin about them takin her cells, now we don't get a dime. I used to get so mad about that to where it made me sick and I had to take pills. But I don't got it in me no more to fight. I just want to know who my mother was.
----Deborah Lacks
When I tell people the story of Henrietta Lacks and her cells, the first question is usually Wasn't it illegal for doctors to take Henrietta's cells without her knowledge? Don't doctors have to tell you when they use your cells in research? The answer is no--not in 1951, and not in 2009, when this book went to press.
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Her name was Henrietta Lacks, but scientists know her as HeLa. She was a poor Southern tobacco farmer, yet her cells--taken without her knowledge--became one of the most important tools in medicine. The first "immortal" human cells grown in culture, they are still alive today, though she has been dead for more than sixty years. HeLa cells were vital for developing the polio vaccine; uncovered secrets of cancer and viruses; helped lead to in vitro fertilization, cloning, and gene mapping; and have been bought and sold by the billions. Yet Henrietta Lacks is buried in an unmarked grave. Her family did not learn of her "immortality" until more than twenty years after her death, when scientists began using her husband and children in research without informed consent. The story of the Lacks family is inextricably connected to the dark history of experimentation on African Americans, the birth of bioethics, and the legal battles over whether we control the stuff we are made of.

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