Reviews tagging 'Ableism'

The Immortal Life of Henrietta Lacks by Rebecca Skloot

17 reviews

jodean's review against another edition

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dark emotional informative inspiring reflective sad slow-paced

4.5


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memento_vivere's review against another edition

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emotional informative reflective

4.75


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moniipeters's review against another edition

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adventurous challenging dark emotional hopeful informative inspiring reflective sad tense slow-paced

5.0


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zams's review

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challenging dark emotional informative inspiring reflective sad tense medium-paced

5.0

English: Definitly the best book I've read so far.
The telling of the stories as well as  the presentation of the researched data was incredible. As somebody who only learned English as a 2nd language I was a little nervous about the presence of authentic language, but it made the whole bok just a lot more real and therefor enjoyable.
An absolutely outstanding work by everybody that contributed. This is not just a book about science but also one that transfers heavy emotins right through the pages.

Deutsch:  Definitiv eines der besten Bücher die ich bisher gelesen habe.
Das Erzähle der Geschichten genauso wie die Präsentation der gesammelten Daten sind unvergleichlich.
Ich hatte zuerst etwas Respekt vor der Tatsache dass authentische Sprache in dem Buch verwendet wird, allerdings war das Verständnis absolut kein Problem, und gab der Geschichte das gewisse etwas, dass sie so persönlich macht. Ich weiß nicht wie diese Parts in der deutschen Übersetzung wirken.
Definitv eine herausragende Arbeit von allen, die daran mitgewirkt haben. 
Nicht nur ein Buch über Wissenschaft, sondern auch eines dass es schafft, heftige Emotionen durch die Seiten zum Leser zu transportieren.

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lunemaline's review against another edition

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emotional informative reflective slow-paced

5.0


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graceburke's review against another edition

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challenging emotional informative inspiring sad tense medium-paced

5.0

One of, if not the most impactful book I've ever read. Rebecca Skloot is a thoughtful and thorough writer as she tells the story of Henrietta, her family, and her cells. I knew very little of Henrietta and her story when I started. I'm not very knowledgable about science in general, let alone cell culture , but this book was extremely accessible. Moving between telling the past life of Henrietta, the present life of her children, specifically her daughter Deborah, and the immortal life of her cells, Skloot shares the horrors and racism of the world through medical practices and the treatment of the Lacks family. She forces you to think about the morality of different medical practices through an in depth exploration of the advancements of medicine on the backs of Black and Brown people. Where does the line between public responsibility and personal rights stand? Do the ends justify the means? Is fiscal compensation enough of a form of reparations? 
The story of Henrietta and her family is complex, Deborah would be one of the first people to admit such. It's hard and harrowing. The duality of distrust for the abuse their family endured and the recognition that it was Lacks' cells that allowed for the saving of millions of lives and counting globally is not lost on them. 
I gasped, cried, and laughed. Deborah and Skloot's relationship is something I will be thinking about for a long time. I'm so grateful the Lacks' story has finally been shared. 

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grboph's review against another edition

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challenging informative reflective medium-paced

5.0

I had to read part of this book as part of a project on bioethics for an anatomy and physiology class, but it was so interesting and well-written that I decided to read the entire thing. I'm very glad I did!! The story of Henrietta Lacks, her cells, and her family is a very fascinating one, and Skloot tells it very well. I really liked that she included herself as a secondary "character" in the book - this served to make the rest of the events of the story and the people she met seem more real because her interactions with them were documented. I learned so much from reading this book about cell biology, genetics, bioethics and its history, medical racism, and so many other things. It's very important this book exists, as it tells the story of a woman whose life affects everybody (due to how ubiquitous HeLa cells are) and how the way she was treated by Johns Hopkins doctors affected her and her family. It also raises a lot of very important points about informed consent and financial compensation, and how attitudes about these things have shifted over time. This was a very informative and well-crafted book, and I would recommend it to just about anyone, but especially anybody who is interested in medicine, biology, and bioethics.

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afion's review against another edition

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kennedybullen's review against another edition

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challenging dark emotional informative reflective sad fast-paced

5.0


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becca_w_'s review against another edition

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challenging emotional informative reflective sad slow-paced

3.75


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