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Henrietta Lacks Discussion Questions

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Participation Portfolio 1 Asst 3: Henrietta Lacks Discussion Questions Please answers each of the following questions, and be prepared to discuss in class 1. Please outline the history of Henrietta Lacks 's tissue cells. Who did what with the cells, when, where and for what purpose? Who benefited, scientifically, medically, and monetarily? 30year old Henrietta Lacks underwent radiation treatment for cervical cancer at the Johns Hopkins Hospital in Baltimore In 1951. During her treatment, George Gey the surgeon who performed the procedure removed pieces of her cervix without her knowledge and sent them to a lab. Her cells were used to develop the polio vaccine, used in the first space missions to see what would happen to human cells in zero gravity. Henrietta’s cells were the first human cells ever cloned, some of the first genes ever mapped. They have been used to create some of our most important cancer …show more content…

What are the specific issues raised in the book—legally and ethically? Think about the 1980s John Moore case: the appeal court decision and its reversal by the California Supreme Court. Issues that raised in the book are race issues, the legality of taking adventage of patients who’s family aren’t able to fight for the rights and benefit of their cells. According to California supreme court, Under the duty to obtain informed consent, “a doctor must disclose his intent in using a patient for research and economic gain.” 6. Should patient consent be required to store and distribute their tissue for research? Should doctors disclose their financial interests? Would this make any difference in achieving fairness? Or is this not a matter of fairness or an ethical issue to begin with? I do think that patients consent should be required, because I think everyone have the right to decide whether or not they want a part of their body used for research. And I think people should be compensated for their contribution to science and the public

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Henrietta Lacks was a thirty-one year old African American who had five kids and married her cousin David Lacks. Henrietta was diagnosed with cervical cancer, the doctors never informed Mrs. Lacks that her cells were to be tested on. The Lacks family was certainly not advised that Henrietta 's cells were growing at an incredible rate. Because of this, the cancer cells were shipped and bought across the world. The last 8 months of Henrietta’s death became a piece of history nobody would ever want to forget.

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Henrietta Lacks Honor Essay “The reason Henrietta's cells were so precious was because they allowed scientists to perform experiments that would have been impossible with a living human. They cut HeLa cells apart and exposed them to endless toxins, radiation, and infection. They bombarded them with drugs, hoping to find one that would kill malignant cells without destroying normal ones.” (58)”Throughout the book “The Immortal Life of Henrietta Lacks” there are many examples of how the HeLa cell of Henrietta Lacks provided cellular information and examples that helped mold many cellular discoveries and experiments.

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After leaving the hospital, she went back to life as usual.” (Skloot 42) The issue of racial inequality in the medical field is further demonstrated by Henrietta’s cells being used to create a multi-billion dollar industry while her family never received any compensation. Even though HeLa cells were used in multiple scientific advancements, such as creating the polio vaccine, Henrietta’s family was still left in

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502 Words | 3 Pages

The event that gave the Lacks knowledge of Henrietta’s cells was when “Gardenia’s brother-in-law, [said] Hopkins had part of Henrietta alive and scientists

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“In 1999, president Clinton’s National Bioethics Advisory Commission (NBAC) issued a report saying that federal oversight of tissue research is “inadequate” and “ambiguous”. It recommended specific changes that would ensure patients’ rights to control how their tissues were being used.” (page 327). Unfortunately, the changes were never made and scientists still have the ability to conduct research on one’s tissues without consent. The reason for why the changes were nullified remain unknown even to Wayne Grody an individual “who was in thick of the debate in the nineties, (for) why the congressional recommendations and NBAC report seemed to have vanished.”.

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1039 Words | 5 Pages

Lacks’ cells were special, in that they would never die and always reproduce, creating medical miracles! Rebecca Skloot’s The Immortal Life of Henrietta Lacks provides many facts about her cells

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823 Words | 4 Pages

From then on, she began seeing a doctor in John Hopkins hospital for check-ups and treatments for cervical cancer. During one of her treatments, a doctor took a sample of her “knot” and passed it on to another doctor in the building to test it. This doctor was named George Gey, and he was trying to make the first immortal human cell line. However, every time he tried, it just did not seem to work. When Gey’s assistants began to grow Henrietta 's cells, they expected them to just die.

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Through her cells we see the impact it created in medical research and understand ethical issues that arose from this experience. I, as many others in the world, strive for an answer on how to stop cancer from occurring and curing it once and for all. 1951 in Baltimore, Henrietta Lacks was a beautiful 30-year-old mother of five children who went to the gynecologist because of spotting between monthly cycles. On examination a lesion was found on her cervix that was biopsied for pathology and found to be epidermoid carcinoma of the cervix, Stage I cancer. This was an interesting case because when Henrietta’s cancer cells were tested they weren’t like other cancer cells; they were aggressive and grew very rapidly.

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239 Words | 1 Pages

Henrietta Lacks was a black tobacco farmer from the south who, in 1950, at the age of 30, she was diagnosed with aggressive cervical cancer. Lacks went to John’s Hopkins medical center for treatment for her cancer. In April of 1951, she underwent surgery to remove the larger tumor on her cervix. Henrietta Lacks, died three days following the surgery. Even though Henrietta Lacks died, her cells from the tumor have lived on and have made a major impact on the biomedical community.

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1020 Words | 5 Pages

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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743 Words | 3 Pages

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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462 Words | 2 Pages

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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512 Words | 3 Pages

Jasmine Poole The Immortal Life of Henrietta Lacks by Rebecca Skloot is about a women who has cervical cancer that went to the doctor to get better. But instead of just getting better, the doctors took a sample of the cancer cells. The doctor used her cells to help other people with the same cancer get better. In this case, Henrietta and her family didn’t know that her cells were being sold all around the world to reporters/doctors.

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860 Words | 4 Pages

She would go to Johns Hopkins for treatment of her cancer to make her more comfortable. At this time, Doctors and Lab Scientists from Johns Hopkins were looking to create cells that can reproduce outside of the body. They would take cell samples from their patients to test them and create a human cell living outside of the body. When Henrietta Lacks died in October of 1951, a lab attendant discovered that, “A swab of Lacks’ cancer cells reproduced at an extremely fast rate…most cancerous cells died within a few days, Lacks’ cells doubled every 24 hours” says the National Women’s Hall of Fame. Henrietta’s cells were determined immortal and were named HeLa cells to represent Henrietta Lacks.

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608 Words | 3 Pages

Yes people should have ownership and control over where and how their tissue is being used. It is my body and if you are going to take something from me, I want to know what you are going to use it for. If it is research, I want to know what type and if it is for potential medical discoveries, I want to be compensated for my “donation”. It is not just knowing that my tissues could be used for medical research. It is having a say as to where my tissue is being studied.

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