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What Are The Ethical Issues In The Immortal Life Of Henrietta Lacks

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The novel The Immortal Life of Henrietta Lacks is based on a poor black woman named Henrietta Lacks who had cervical cancer in 1951. Although such a wide range of cancers all across the United States were present during her time, she, in fact, her cells, were selected and collected without consent or knowledge to develop a so called “immortal cell.” This “immortal cell” has been sold in the billions, in which the Lacks family has received absolutely nothing in return for. They were unknown and unheard of. However, the research and understanding of her cells in order to develop vaccines, immunity, cloning, etc. is the base of some parts of modern biology and medical research today. But, this of course came with major ethical issues which was exceptionally well written and explained. Alongside the …show more content…

Cite literature or research that is in conflict with the author's position Summarize and cite it here.
"The Immortal Consenting of Henrietta Lacks." It Is NOT Junk. Web. 18 Aug. 2015.

On the citing listed above, Rebecca Skloot herself discusses her book with the devil’s advocate.

5. How did your reading and research on this idea change your understanding of this topic?

It helped me develop thought provoking details about the history of biology, and other problems within the world that may have been “resolved” using unethical resources.
4. Do ethical issues, in such an extent to Henrietta Lack’s situation, still occur today? 1. Why is this question important to you?
Curiosity and also to find out whether or not this “corruption” is still present in the medical field, and if so, to a lessened or greater extent?

2. What are the implications of the question? To develop a comparing point of view to Henrietta Lacks.

3. Search for literature or research that will help you answer this question. Summarize and cite it here. Explain

Lo, Bernard, and Lindsay Parham. "Ethical Issues in Stem Cell Research." Endocrine Reviews. The Endocrine Society. Web. 18 Aug.

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Not only would her cells be important, but also, these cancer cells would cause her family to go through many challenges. Though Henrietta’s might have not been and important person while being alive. She & her family live through her reproducing cancer cells that continue to create advancements in the medical field. Mrs. Lacks “showed up at Hopkins complaining

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Would people in 1951 feel any different if they knew black people could produce lifesaving cures with technology? Henrietta Lacks was a black woman that got cervical cancer and went to Hopkins hospital because it was the closest segregated hospital around. While Henrietta was as Hopkins, they were doing tests and during that process, Dr. Gey took Henrietta’s cells without her consent. Henrietta was diagnosed with Cervical cancer doctors took samples without her consent. She had five kids and died at Hopkins hospital on October 4, 1951 being only 31 years old.

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Rebecca uncovers that when Henrietta received treatment for cancer, a sample tissue was cut from the tumor growing in her cervix without Henerietta’s knowledge. Dr. TeLinde, the leading doctor in the study of cervical cancer, took tissue samples from women in public wards without their consent. This was common practice back in that time, and TeLinde figured that it was a fair exchange since the people in the public ward of Hopkins Hospital were receiving treatment without payment. Skloot lets us know that TeLinde was in the middle of proving that invasive tumors developed from noninvasive tumors. His research would be further helped by Gey and Margaret, who worked for over 30 years in producing an immortal lineage of human cells outside of the body.

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When doing research like the author of this book did, it is easy to get caught up in all of the information and forget it is from 70 years ago. What Henrietta’s doctors did to her is unthinkable now, but it didn’t happen in 2023, it happened in 1951, and back then the laws and acceptable practices were different. That does not excuse behavior, but it is still important to keep in mind. V. Further reading/ Additional Information 1.

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The themes in the novel tell a complete story of life, science, and the science of life. “It was very dehumanizing to be thought of as Mo, to be thought of as Mo in the medical records: ‘Saw Mo today.’ ” (Skloot 201). This animal like referral to patients then demonstrates just how far medical ethics has come. It also proves that these dehumanizing tactics are a major theme in the story.

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In the 1950s the first ‘immortal’ human cells were grown from a cancerous tissue sample taken from Henrietta Lacks, a poor black woman, without her knowledge or consent. She had died shortly after, at the unfortunately early age of 31, of a severe case of cervical cancer. Henrietta had a list of ailments that included neurosyphilis, gonorrhea, and HPV the leading cause of her cervical cancer and, ultimately, her death. The hospital that had diagnosed her cancer, Johns Hopkins, had supposedly been one of the best hospitals in the country, but it participated in discriminatory and amoral research practices when treating African Americans. Not only taking taking Henrietta’s cells without her consent, but injecting them and other cancer cells into patients without their knowledge.

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During my University 111 class, I was given the opportunity to read the Immortal Life of Henrietta Lacks. This read was connected to the most important medical breakthrough of the 20th century that changed the face of scientific research. This was the discovery of the numerous uses of cancerous cervical cells from a colored woman named Henrietta Lacks, to science she was HeLa. Her cells aided in the understanding of the development of AIDS/HIV treatment, the development of the polio vaccine, understanding the nutritional needs of cells, and stronger requirements of patient consent laws. To better understand the reading, the class was assigned a project that would allow us to make societal connections.

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Skloot brings attention to the lack of informed consent and the exploitation of marginalized populations in medical research. The story of Henrietta Lacks and her HeLa cells illustrates the ways in which individuals can be reduced to mere resources for scientific progress, without proper acknowledgement or compensation for their contributions. Skloot's book also highlights the importance of acknowledging the humanity and dignity of individuals who have been used for medical research. This is particularly relevant when dealing with marginalized communities, who have historically been exploited and mistreated in medical research. By bringing these issues to light, Skloot raises important questions about the responsibility of the medical community to prioritize the well-being and dignity of all individuals.

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Henrietta was a victim of the unethical methods that took place at John Hopkins hospital. She was violated when they decided to take her cells without her permission, and she was never told that they had taken her cells before she passed away. After, Henrietta passed away her family suffered greatly. Her husband, Day, did not take care of the children well. Henrietta was the only one in the family who visited Elsie, who was at Crownsville State Hospital, which was an hour and a half south of Baltimore (Skloot 45).

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Lacks, was a woman who had her life taken by cancer. However doctors and scientists began to notice that her cells continuously produce (to this day in fact). Henrietta’s family was not informed about her “immortal cells” until 20 years after her death. To all readers disappointment, her family didn’t even get a portion, or even a small percent of the money earned from using her cell line to make various medical advances. These include the polio vaccine, the cancer drug tamoxifen, chemotherapy, gene mapping, in vitro fertilization, and treatments for influenza, leukemia, and Parkinson’s disease (from article).

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In today’s world people are endowed to full rights when it comes to their medical wellbeing. When seeking medical care from physicians and professionals we expect a full explanation of our health and possible treatment plans. It is even law that we provide informed consent before proceeding with care. “The Immortal Life of Henrietta Lacks” by Rebecca Skloot is a thought provoking novel that takes a close and personal look at the story of Henrietta Lacks and her family. She is an African American woman whose cells were used for the advancement of medicine, all without her knowing.

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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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Racism in The Immortal Life of Henrietta Lacks Imagine your mother, sister, wife, or cousin was diagnosed with cervical cancer and you believed the doctors were doing everything in their power to help her. Only later you discovered her cells were used for research without consent and she was not properly informed of the risks of her treatment due to her race. This story happened and is told by Rebecca Skloot in The Immortal Life of Henrietta Lacks. Skloot use of narrative and her writing style enhances the understanding of the story. Henrietta Lacks was a young black woman who was diagnosed with cervical cancer at John Hopkins Hospital.

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The final violation of ethical principles, in the story of Henrietta Lacks, was the violation of justice. Without the contribution of Henrietta’s cells, many discoveries and vaccines, such as the vaccine that conquered Polio, would not have made their pivotal breakthroughs in biomedical research. Her direct and unknowingly, supportive contribution helped save many people’s lives all over the world. Unfortunately, her named did not receive the recognition it deserved, and her family never received any compensation for profits made from direct use of her

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