The scientific community and the media are guilty of viewing Henrietta and her family as abstractions; they did not give the Lacks family a fair trial, they’ve yet to give her family any form of compensation for the success of her cell line, and operated on Henrietta like a science fair project. In the non-fiction narrative The Immortal Life of Henrietta Lacks, written by Rebecca Skloot, it states, “The fact that no one had sued over the growth or ownership of the HeLa cell line, he said, illustrated that patients didn’t mind when doctors took their cells and turned them into commercial products.” (204) This is unfair to the Lacks family because the fraud lawyer, Keenan Kester Cofield, deceived them. Although he is a con artist, he has a wide spectrum of knowledge about law than the Lackses really have about anything; they’ve had little to no education, and they barely knew anything about the HeLa cell line. The media made it seem as if the Lackses …show more content…
I thought, Oh jeez, she’s a real person. I started imagining her sitting in her bathroom painting those toenails, and it hit me for the first time . . . those cells we’d been working on came from a live woman. I’d never thought of it that way.” (91) They finally began to realize that Henrietta was not a toy; she was a real human being with a life, a family, and thoughts of her own. The fact that she was an under class, black woman in the 1950s made her less of a human. So doctors didn’t treat her fairly like they would someone with a lighter shade of skin. These three ideas relate to each other because it shows how people didn’t bother to get to know Henrietta or the Lacks family until real profit was involved; and the only real time they’d attempt to “contact” the family was to ask for the permission to have Henrietta’s medical records, or it’s bothersome reporters constantly asking them questions that they wouldn’t know the answer
On the topic of respect, there was also a lack of respect related to her family. The Lacks family were not all on board for the usage of HeLa cells. Infact, not until about 20 years later did the scientist have the audacity to mention it to them. When Henrietta’s children were informed that her mother's cells are still living today, they were very rudely informed. The scientists wanted more information about Henrietta, so they went to her children to collect more blood samples.
The Immortal Life of Henrietta Lacks is a strong illustration of the interplay between race and medicine. After reading this book, I thought that I probably owe Henrietta Lacks for my some of the medications or treatments I have received in my life. It is unfortunate that Henrietta and her family were treated
Lance Langel 11/18/14 P.8 Bibliography Fahy, D., & Nisbet, M. C. (2013). Bioethics in popular sciance: evaluating the medica impact of The Immortal Life of Henrietta Lacks in the biobank debate .Retrievedfrombiomedcentralhttp://www.biomedcentral.com/1472- 6939/14/1 Due to biobanks, there has been many bioethical concerns regarding, disclosure, ownership, privacy, control, and consent. As an opportunity to engage an audience about these ethical issues, bioethicists have used Rebecca Skloot's book "The Immortal Life of Henrietta Lacks" (Fahy & Nisbet, 2013). To engage the audience, researchers conducted an analysis of relevant articles and transcripts produced by organizations and publications in the U.S. and in other countries (Fahy & Nisbet,
Ultimately, I contend that all multitude of instances that the Lacks family was taken advantage of set the foundation for Deborah to trust Skloot. Unlike the other news reporters, authors, or doctors that approach the Lacks family, Skloot made an effort to connect with the family by spending time with Deborah’s cousin cliff, and walking Henrietta’s tobacco fields. Moreover, Skloot was one of the first writers that aimed to focus more on the Life of Henrietta, instead of HeLa cells. When Deborah first accepts Skloot, Skloot realizes that the media completely perplexed the Lacks family. Despite everything that had occurred, the Lacks family still did not have a defined understanding on what HeLa cells actually were and what they were used for.
After all it was back in time where the colored weren’t treated equally, so they never had a chance of getting any money from the HeLa cells. Some members of the Lacks family, who had made peace with Hopkins after learning in the 1970s that it had taken Henrietta’s cells, now planned to sue the Hospital for taking the cells without permission. They accepted it and now they had to live with it, with knowing that their mother's cells were being sold to people around the
Deborah states, "Truth be told, I can 't get mad at science because it help people live, and I 'd be a mess without it. I 'm a walking drugstore! I can 't say nuthin bad about science, but I won 't lie, I would like some health insurance so I don 't got to pay all that money every month for drugs my mother cells probably helped make". This explains how Deborah has to spend all her money on not even all her medication because she can 't even afford health insurance that will cover her medicine. African Americans who were
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.
On January 29, 1951, an African American woman named Henrietta Lacks was diagnosed with Stage 1, Epidermoid carcinoma of the cervix, after her visit to John Hopkins Hospital. Henrietta began radium treatments which was proven to kill cancer cells and a safer option than surgery, according to her physician Howard Jones. Jones increased Henrietta’s dose of radiation in hopes to decrease the size of the tumors however the treatments were proven ineffective and her skin was burned blacker while the pain grew unbearable until she passed away on October 4, 1951. She left behind her husband David “Day” and five children: Lawrence, Elsie, David Jr, Deborah, and Zakariyya (Joe). This paper will focus on how Henrietta Lack’s and her family’s experience
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.
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.
And once hospitalized, they got fewer pain medications, and had higher mortality rates” (Skloot 64). Because of racism and discrimination, Henrietta may have likely received improper care for her cervical cancer and an abuse of her cells by big pharmaceutical companies. Skloot not only addresses the pain of Henrietta’s family in the unjust use of HeLa cells, but also of one of Gey’s lab assistants, Mary Kubieck. Mary is confronted with the humanity of HeLa cells during an autopsy when she see’s Henrietta’s red painted toenails, “I started imaging her sitting in her bathroom painting those toenails, and it hit me for the first time that those cells we’d been working with all
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.
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.
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
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