Henrietta Lacks Book Report

Throughout the book The Immortal Life of Henrietta Lacks, many social justice issues were presented. One of them was racial discrimination, specifically in the medical world. Race was perceived in an extremely different way than it is now; it is clearly evident how it impacted the medical care that Henrietta Lacks received and what happened with the family as her cells were spread and studied. Today the situation would be handled differently. There are not segregated hospitals with people saying that since a person does not have enough money to pay for a hospital visit, taking tissues and cells from the body is okay. Racial discrimination in the medical world has changed a great deal since the time that the HeLa cells were first taken.

Can you imagine going to the doctor and doing whatever that doctor told you was the best for you without asking questions? Well that is what patients did in the 1950s, especially African Americans, who were still being victims of racial prejudice and segregation. In this book, the author, Rebecca Skloot tells us about Henrietta Lacks, a 31 year old African American woman who was diagnosed with cervical cancer, and trusted her doctors, who took a sample of her cells without her knowledge. These cells would help in scientific discoveries that helped millions of people. Henrietta died of cancer and her family is devastated when they find out that the cells had been taken without permission, and that they were being sold for profit.

The non-fiction book The Immortal Life of Henrietta Lacks, written by Rebecca Skloot, details the happenings and life of Henrietta Lacks, an African American woman and tobacco farmer who became a medical miracle in the 1950’s. The book is written in an attempt to chronicle both the experiences and tribulations of Henrietta Lacks and her family, as well as the events that led to, and resulted from, research done on Henrietta Lacks’ cells. Henrietta was a very average African American woman in this period; she had only a seventh-grade level education, and followed traditional racial and gender roles by spending her time has a mother and caretaker, as well as working on farms throughout her life until the involvement of the US in World War II brought her and her husband, “Day” Lacks, comparatively better work opportunities in industrial steel mills. However, after her death in 1951 Henrietta became much more than average to doctors at John Hopkins when the discovered that cells extracted from her cancerous tissue continued to live and grow much longer than any other tissue samples. Further investigation and isolation of these thriving cells led to the creation of the first ever immortal human cell line in medical history. The incredible progress in medicine made possible by Henrietta Lack’s tissue cells were not without downfalls, though. The treatments and experiences received by Henrietta and the effects it had on her and her family demonstrate both racial and gender

The Immortal Life of Henrietta Lacks is a true story of a poor, Southern African-American tobacco farmer who died in 1951 at the very young age of 31 years old from cervical cancer. Little did she know that cells harvested from her tumor, which were obtained without her consent have lived on and on and became one of the most important tools in medicine today. Despite Henrietta’s story being full of legal and ethical issues, the story was one filled with success and anguish. Success for science as her cells served as advancement in medical research and development; yet was sorrowful for Henrietta and her family. This story occurred during a time of segregation in the United States, when Henrietta Lacks believed she

In her book, The Immortal Life of Henrietta Lacks, Rebecca Skloot discusses how one woman’s unfortunate diagnosis of cancer resulted in the discovery of the first immortal human cell line, HeLa. The establishment of the HeLa cell line has proven to be one of the most influential breakthroughs in the biomedical sciences because these cells have played a major role in some of the largest breakthroughs in since they were first cultured in the 1950s. In addition to an examination of the science behind HeLa cells, Skloot also provides a look at the lives of Henrietta Lacks’s descendants. One characteristic that all members of the family share is a dedication to religion and spirituality. This juxtaposition between science and religion presents the body and its constituent cells in a unique way. It provides multiple dimensions to how people can view bodies. Specifically, Skloot’s depiction of HeLa cells presents the body and its individual cellular components as entities that exist as both scientific and spiritual beings simultaneously.

Bobette met a research scientist who said he had been working with cells from a woman named Henrietta Lacks, Bobette’s reaction can be seen here, “But Bobette kept shaking her head saying, ‘how come nobody told her family part of her was still alive?’ ‘I wish I knew’ he said. Like most researchers, he’d never thought about whether the woman behind the HeLa cells had given them voluntarily’” (Skloot 180). The research scientist she talked to, along with countless other scientists, had never thought about the woman behind the cells and this is part of the reason nobody ever told the family about the cells. Bobette finally found out about the HeLa cells after twenty-five years of no information and a revolution in medicine caused by her late mother-in-law. But it did not get better for the Lacks family after discovering Henrietta’s cell line. Every time one of the Lackses asked questions about Henrietta’s cells, the professionals would never take time to answer their questions, to help them understand what had happened at Johns Hopkins with the cells, or to explain to the Lackses what Henrietta’s cells accomplished. The doctors did not care about the patients and their families, but more about what was in it for them. The doctors did not look at the situation ethically by not telling the family about the cells. They also violated privacy values, which are now rights. They

Henrietta Lacks case was different than Mississippi and Tuskegee in some ways. In Henrietta’s case the doctors took her cells from her cervix but like in the Mississippi and Tuskegee cases they took them without Henrietta’s permission and launched a multimillion-dollar medical industry after she died. The purpose of taking Henrietta’s cells was to just run a couple tests until they died but they ended up living and growing. Instead of telling Henrietta and her family what they have been doing the doctors kept the discovery to themselves. When the discovery of the immortal cells because known every doctor got their hands on them and started running experiments on them, sending the cells to space, running test on the cells to find a cure to aids and cervical cancer etc…

Henrietta Lacks is woman, whose cells have been used for 63 years after her death in 1951, and will continue to be used as long as they are continue to grow. Henrietta Lacks was an African American woman who was born in the south, who married her cousin and moved up north. After giving birth to her last child, she finds that she has cancer. The doctors took a sample of her cancer cells without her permission, and now have millions of dollars but the family is still hasn’t received the money they are rightfully entitled to. Many of healthcare and entitlements that are around today, are due to the ill treatment of Henrietta and her family. Still to this day, there is very little known about Henrietta Lacks, even with the book out, and she has

The Immortal Life of Henrietta Flacks tells the journey of scientific advancement in both a legal advancement capacity as well as an ethical advancement capacity. As if what I could only imagine being and African American woman in the 1950’s in Baltimore City isn’t hard and complicated enough; being and African American woman and seeking medical treatment without knowledge of the sickness without a voice or understanding of the gravity of the situation must be an excruciating experience and was for Henrietta Lacks and her family.

The “The immortal life of Henrietta lacks” is a biography of all the events that happened surround the discovery, experimentation, and aftermath of the HeLa cells. This book goes in depth not only about the cells but the lacks family. In 1951 after her daughter Deborah was born Henrietta she talk to her cousins and some friends and described the feeling of “a knot” inside of her. Months after

After her death in 1951, for six decades, Henrietta Lacks did not exist in the eyes of the society, but her cells did. How? Well, the answer is quite simple. HeLa Cells are the first immortal human cells. These cells never die and multiply every twenty-four hours. After spending 10 years to perfect her first book, author of The Immortal Life of Henrietta Lacks, Rebecca Skloot essentially captured the life, the death, and aftermath of Henrietta Lacks’ life. With controversial issues regarding science, ethics, race, and class Skloot takes us on an extraordinary journey. From the “colored” ward of Johns Hopkins Hospital in the 1950s to stark white laboratories with freezers full of HeLa cells, from Henrietta’s small, dying hometown of Clover,

“Skloot traces the changing ethics and law around tissue collections, and the inadvertently careless journalists and researchers who violated the family’s privacy by publishing everything from Henrietta’s medical records to the family’s genetic information.” (Margonelli). Skloot thoroughly explains how these laws effected the Lacks family and how their case led to medical ethics and law changes. The authors main purpose for including this was to share the Lacks’ story and their experience with immoral medical ethics. Another main point explained throughout the book is medical science. With the discovery of HeLa cells science began to have a rapid rate of new discoveries and cures to other diseases. “The reason Henrietta’s cells were so precious was because they allowed scientists to perform experiments that would have been impossible to perform with a living human. They cut HeLa cells apart and exposed them to endless toxins, radiation, and infection.” (Skloot 58). Skloot explains that without Henrietta’s cells science would not have evolved to what it has become

Henrietta Lacks: an unknown name up until recent years. A name that had been known to the world only as HeLa; The first two letters of a name that belonged to a poor African American tobacco farmer that unknowingly changed science and life as we know it today. Her life has finally been portrayed in a very intimate story that not only does her life some justice but also transcendentally brings to mind the philosophical issues concerning medical ethics both of the past, present, and the future. In a world of constantly evolving medical advancement, science is a pivotal force that propels ideas forward. Although most will agree that the knowledge and cures found are a positive aspect, there is also a necessary evil that is involved, including

Rebecca talks about whether or not people should have the rights to their own tissues. She points out two issues, consent and money. In the past there was no informed consent, so the doctors and researchers felt free to use tissues in whatever way they wished, with little concern for patients' rights. Nowadays there is a different system, and it's required by the law to ask for a patient's informed consent.mThe money issue is a question of whether doctors should be required to tell patients if their cells or tissues are going to be used for commercial research, and what rights those donors should have. Later on, “scientists sequenced Henrietta Lacks's genome and made it public, without asking the family's permission” which was just another way in which the family was violated and looked over (Silver). Apparently Henrietta didn't get her rights, and neither did her children. Any way we look at it, if the family had received any benefits from the cells, it

The effect the discovery and creation of the HeLa cells made on the science community and Henrietta’s family had a domino effect. Both had different opinions and beliefs on the matter; this led to some difficult questions asked of the family and of the medical community. Due to the new and advanced methods of experimentation, the HeLa cells made to to the field of science, the scientific community and the media failed to remember that Henrietta and her family were not abstractions but actual people. Rebecca Skloot, however, took into account the Lack’s family, she inquired both the history of the HeLa cells as well as the Lacks family, treating them as actual people with inalienable rights.