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The Immortal Life Of Henrietta Lacks By Rebecca Skloot

1514 Words7 Pages

Throughout the Rebecca Skloot’s book, The Immortal Life of Henrietta Lacks, she described her investigation into the life of Henrietta Lacks, her immortal cell line, the ethical violations surrounding her case, as well as the major contributions to modern medicine and research her case provided. During the time of Henrietta’s treatment, both medical and research ethics were quite different; many values such as autonomy, justice, and beneficence were not as enforced, and were applied differently throughout different institutions and individuals of different demographics. Though investigating her case and other important cases surrounding the use of HeLa cells, Skloot acknowledges the unethical circumstances which filled Henrietta’s case and …show more content…

Although I do feel that I am in some way biased from learning and practicing modern ethical principles, I can see the endless ways those surrounding her case took advantage of, violated, and disturbed the lives of both Henrietta and her family. However, for that time those ethical practices were normal for them; they thought were not explicitly hurting Henrietta by using her cells, and they were trying to use their research for good, unlike some research done by the Nazis for …show more content…

A point in the book that really made me recognize this was when Gey’s assistant was performing the sample collecting during Henrietta’s autopsy and she noticed Henrietta’s toenails and became ill remembering that she was a real human who meant something to many people: a wife, mother, sister, and friend. Another interesting observation from the piece is that many of the people working with and benefiting from Henrietta’s cells, did not even know the source of the cells: HeLa aka Henrietta Lacks. At some point in our lives most of us have benefited on some way from research only made possible by her cells, and I personally think that it is a shame that Henrietta’s case is not taught during primary education as I feel it is a crucial part of modern healthcare and history. It is crucial for patients to know their rights and know that they are protected in receiving care, therefore it is important that individuals have a common knowledge of

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Henrietta Lacks was a poor black tobacco farmer,born in Roanoke, Virginia on August 1 ,1920.Henrietta’s mother died when Henrietta was very young, her dad did not wanted to take care of her and her siblings, so they were sent with different relatives. She grew up with her grandfather. Henrietta died at age of 31 years old of cervical cancer, on October 4, 1951. At the age of twenty-nine she felt a “knot” inside of her. In the year of 1950, she had a full-fledged tumor just three months  after she had felt the knot.

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During the 1950’s African American’s had a difficult time living in a world where they were seen to be lesser of a human being than what they were. They were treated differently in normal everyday lives as well as in the medical world. Henrietta Lacks was a woman who was greatly affected by this divide between whites and African-Americans. Because of the color of her skin, I believe she was not treated to the best of the doctor’s ability, and instead just used for indirect experimentation. In Rebecca Skloot’s novel, The Immortal Life of Henrietta Lacks, she gives examples of how African-Americans were treated differently, a few of those include; the conditions of John Hopkins, the African-American medical experiments, and Hector Henry.

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The Immortal Life of Henrietta Lacks overviews the story of a young black woman who dies a painful death duo to an aggressive invasive type of cervical cancer, something doctors were currently studying and developing way to combat it. Rebecca Skloot, the author, takes us to journey to see through the eyes of the Lacks family. Many would call what was done to them unfair, but as Skloot lets us know, this was common practice (and still is in many cases) during that time. The important thing was that the ignorance of who was responsible for the cells that we call “immortal,” the cells that have given us a “Rosetta stone” for medical research, is now diminish, this was especially important to the Lacks. The book focuses mainly on the story of Henrietta’s

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Her cell line is most commonly known as HeLa: He from the first two letters of Henrietta and La from the first two letters of Lacks. Despite this seeming positive outcome, Henrietta, specifically her family were not informed until 20 years after Henrietta's fatal cancer experience. Raising the inquiries: Was this ethical? Should the Lacks family be compensated for their mistreatment? Was the unconsented research on Henrietta lacks lawful?

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The Immortal Life of Henrietta Lacks is a novel by Rebecca Skloot detailing the life of Henrietta Lacks and her family. In her 2010 narrative, Skloot explores the scientific discoveries made through the use of the so-called HeLa cells obtained from Henrietta in her final years, as well as the results of malpractice within segregated hospitals and the effects on the Lacks family. The importance of these topics was only amplified with each new advancement and each new onus transferred to the Lacks family. Consequently, strong held beliefs by both the scientific community and Henrietta’s ancestors clashed. The story of Henrietta Lacks began on a plantation in Virginia in 1920, but the most impactful years of her life came at the end of her time.

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Jade Sherwin May 14th, 2018 Essay test Rebecca Skloot’s book “The immortal Life of Henrietta Lacks” tells the story of Henrietta Lacks a young mother, a descendant of slaves, whose suffering changed the course of medical research and made life healthier for the rest of us. Henrietta was diagnosed with cancer in numerous ways the Lacks family’s right to privacy was violated. The Lacks family’s right to privacy was violated by people exposing the Lacks’s information “Newspapers and magazines “published articles about Henrietta , one of the pivotal figures in the crusade against cancer.”

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Henrietta Lacks’s daughter Deborah once stated “If our mother cells done so much for medicine, how come her family can’t afford to see no doctors?” (Skloot 9). The lack of ethics also points to another theme of Henrietta’s story, discoveries are more than the discovery itself, there are always people behind them. Deborah’s words also emphasize the human side

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Robertson Davies, a Canadian novelist, once wrote, “The eye sees only what the mind is prepared to comprehend.” We have the power to decipher between the images before us and convince ourselves that what we are seeing is truly what we make it out to be. In Rebecca Skloot’s novel, The Immortal Life of Henrietta Lacks, Skloot tells the story of a woman named Henrietta Lacks with immortal cells. Henrietta’s cells were used for science and stirred up turbulent debates between scientists, doctors, politicians, civilians, and others. The ethical backing to the research and testing done with HeLa cells, the abbreviation for Henrietta’s immortal cells, was, and in some ways still is, the main topic concerning Henrietta’s cells.

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Herded onto slave ships, forced into labor, and treated lower than animals, 12.5 million Africans were brought to the New World between 1525 and 1866 and became the foundation of the United States, a country now based on liberty and justice for all. Just because America is a beacon of hope and a symbol of equality in the 21st century, its roots in slavery are not morally justified by its current state. Similarly, Henrietta Lacks’ violation of autonomy at Johns Hopkins may have been accepted back then, but it does not make violating her autonomy any more morally correct. Despite the monumental advances in science that stemmed from Henrietta Lacks’ cancer cells, the violation of Henrietta’s autonomy and the hardships she and her family faced

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I read The Immortal Life of Henrietta Lacks by Rebecca Skloot for the first time in high school for a summer reading assignment I was rushing to complete the last week of summer break. Four years later, I chose to read this book again because I now have an interest in biochemistry, in particular a goal to study antiviral agents in the hopes of a Hepatitis B cure. This time around, I understood the significance this book had because it revealed details of the racist treatment of African Americas that are intertwined with the hidden truths and hypocritical acts of the medical system that unfortunately still exist. On October 4, 1951 Henrietta Lacks died from cervical cancer at the young age of 31.

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Despite the wrongdoings Henrietta Lacks was put through her cells did a lot to help advance science. Her cells helped develop different types of vaccines, which such as her daughter faced. A lot of good and bad came out of Henrietta’s

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The Immortal Life of Henrietta Lacks tells the story of Henrietta, an African-American woman whose cells were used to create the first immortal human cell line. Told through the eyes of her daughter, Deborah Lacks, aided by journalist Rebecca Skloot. Deborah wanted to learn about her mother, and to understand how the unauthorized harvesting of Lacks cancerous cells in 1951 led to unprecedented medical breakthroughs, changing countless lives and the face of medicine forever. It is a story of medical arrogance and triumph, race, poverty and deep friendship between the unlikeliest people. There had been many books published about Henrietta’s cells, but nothing about Henrietta’s personality, experiences, feeling, life style etc.

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Her doctor collected cancerous cells and healthy cells from her cervix and gave them to the cancer researcher, George Otto Gey, who was trying to keep cells alive for more than a couple days. Henrietta endured intense radium treatments, but she still died at the age of 31, leaving her husband and five children behind. An amazing discovery was made Henrietta’s cell were immortal. Racism is prevalent in this book through the limited availability of healthcare, unethical behaviors of the doctors, and how racism affected her family. During this time, there was an extensive lack of medical care for colored people.

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The origination of HeLa cells, used in biomedical research for a potential cure for cancer, had made many ground breaking discoveries in science; all thanks to one woman, Mrs. Henrietta Lacks. The history of Mrs. Lacks’s contribution to these studies raised many ethical issues concerning healthcare practice. In the short film, The Way of All Flesh, we learn how these cells were revealed by direct violation of ethical principles. During the 1950s, matters regarding informed consent practices were in their beginning stages of implementation.

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Bushra Pirzada Professor Swann Engh-302 October 4th 2015 Rhetorical Analysis: The Immortal Life of Henrietta Lacks The Immortal Life of Henrietta Lacks written by Rebecca Skloot tells the story of a woman named Henrietta Lacks who has her cervical cancer. It further goes to tell the audience how Henrietta altered medicine unknowingly. Henrietta Lacks was initially diagnosed with cervical cancer in 1951; however, the doctors at John Hopkins took sample tissues from her cervix without her permission. The sample tissues taken from Henrietta’s cervix were used to conduct scientific research as well as to develop vaccines in the suture.

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