Reviews tagging 'Physical abuse'

The Immortal Life of Henrietta Lacks by Rebecca Skloot

45 reviews

creationwing's review against another edition

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challenging emotional informative reflective medium-paced

4.25

I wasn't a huge fan of the attempts at Chinese and Austrian accents by the audiobook reader. It felt off in a book with themes so closely tied to facing racism. It didn't help that they weren't very well done, either.

There were moments when the book seemed a little too voyeuristic for my taste; I'm not sure that all the details included were necessary for me to learn about this historic figure, her family's struggles, and have understanding of the suffering and unjustice.

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udari's review against another edition

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challenging emotional informative reflective sad medium-paced

5.0


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elizabethgreads's review

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hopeful informative reflective medium-paced

4.0

I enjoyed the way this book was told.  It flips back and forth between the science, history, and ethics of tissue and cell culture and the Life of Henrietta Lacks and her family. This is an incredibility important story that I think everyone should read.  The author does a great job of describing scientific terms in such away that the reader can understand without having much knowledge on the subject. I enjoyed the exploration of the topics of informed consent, medical privacy, research ethics, and commercialization of human cell products.

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julia_ham23's review against another edition

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challenging emotional informative reflective sad medium-paced

4.0


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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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coreyarch9's review against another edition

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challenging emotional informative reflective medium-paced

4.0

"'[It] hit me for the first time that those cells we’d been working with all this time and sending all over the world, they came from a live woman.'"

I recently reread The Immortal Life of Henrietta Lacks since it's my book club's pick for this month.

My life has changed a lot since I first read the book a few years ago and, as such, a few things hit differently this time around. For one, Henrietta was 31 when she died. Now in my thirties, myself, this detail stood out so much more. Additionally, I've since benefitted greatly from the lifesaving diagnostic testing that her cells specifically helped develop. Throughout the book, I couldn't help but reflect on some of my own health challenges from the past year, which at times were triggering.

Just as during my previous read, I often went straight to Wikipedia to learn more. Specifically, as I was looking up historical information on John Hopkins, I got the clearest sense of deja vu, a confirmation that similar details and curiosities stood out to me both times.

I'm am looking forward to my book club's discussion later this month. If you've read this book, then you understand the hodgepodge of thoughts and reactions that I'm currently experiencing.

•••
My original review:
This book had been on my list since I first heard about it on NPR and WOW DID I LEARN A LOT. I found myself scouring through Wikipedia pages more than a few times over the course of reading. My only criticism is that sometimes the author gets caught up in describing her process for investigating Henrietta Lacks and forgets to progress the story. This book is for anybody who enjoys ethical debates, cares about social issues, and enjoys medical dramas/family dramas/ literally any type of drama.

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mandi4886's review

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emotional informative reflective sad tense medium-paced

5.0


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booksjessreads's review against another edition

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5.0

What. A. Book. This is genuinely one of my favourite books ever.  This book tells the life story of Henrietta Lacks (aka HeLa) who's 'Immortal cancer cells' were used to test treatments for polio, helped discover HIV, and helped us find out that transplanted organs are rejected in a new body by the immune system and not because of different DNA. Her cells still live today.

Henrietta Lacks was a 31-year-old black woman with 5 children when she died from cervical cancer. Howard Jones, her doctor, took a sample of her cancer without her knowledge or consent and shipped it off to a lab where it kept growing and growing. Researchers took advantage of this, but kept Henrietta's family in the dark about medical research taking place because of her.

Rebecca Skloot tells this story so amazingly. Half of the book is Skloot telling us how she acquired the information about Henrietta, and the other half is telling us about Henrietta's life, all combined to make the book. Skloot does the story justice, showing the hardship the family faced in light of all the secrets kept from them. She talks about the ethics of taking cells without consent, the crippling racism the family faced in 1950s America, and centre's the voices of the family and Henrietta, rather than imposing her own narrative throughout the story.

A side note that half of the proceeds of the book go to Henrietta's family. The family didn't receive a single penny of the medical research or sales of Henrietta's cells, so if you ever get a chance to read the book, I encourage you to buy it (if you didn't need encouraging enough!)

Honestly such an incredible read and certainly one of my absolute favourites this year! 

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foreverinastory's review against another edition

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emotional informative sad

5.0

Everyone should read this book, but especially the scientific field.

CWs: Abandonment, ableism, addiction, blood, cancer, child abuse, chronic illness, death, death of parent, drug abuse/use, emotional abuse, fatphobia, forced institutionalization, grief, incest, infidelity, medical content, medical trauma, mental illness (PTSD), physical abuse, pedophilia, pregnancy, racial slurs, racism, rape, sexual assault, sexual content, sexual harassment, terminal illness, vomit. 

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angelaf's review

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challenging informative sad slow-paced

2.0

The story of Henrietta Lacks and HeLa cells is a very important story to tell due to its historical significance and the ethical issues it raises. However, I often felt bogged down in all the details and felt like I would have been more engaged with the book if it was 75-100 pages shorter. Also, I felt somewhat icky while reading about the Lacks family since the narrative felt rather invasive at times. I think the story could have been told without exposing the family so much. In some ways, the book feels like more white people profiting from and exploiting the Lacks family. Read if you enjoy: medical history, narrative nonfiction, untold history

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