fend for themselves, despite being relatives to one of the most important individuals’ in cell-line history. Now, knowing the full potential of these cells, the question arises of why the Lacks family was not told of the cells by the scientists themselves. Many possibilities arise, but the main one is that the existence of the cells would have gone against the wishes of the family. The sample of the tumor was taken before Henrietta died, but permission to perform tests was only requested after her death. Additionally, the permission was initially not granted by Day, her husband, to perform any additional test on her body. He reluctantly gave in, but he was under the assumption the tests were being performed to prevent a similar disease in …show more content…
From helping create vaccines to the diagnosis of genetic disease, the cells were very useful in medical research. The existence of the cells was concealed from her family, both to allow the research to go uninterrupted and because the identity of the person behind the cells remained a public mystery. Even after the truth came out, the family did not receive any special medical care or assistance, despite being related to Henrietta, who made many of the medications and medical procedures possible through her cells. This may have been an effort to observe any possible effects that a genetic HeLa presence would have on an individual, at the risk of the well-being of the individual. Stemming from this controversy, debate regarding the moral obligation that individuals have to provide their cells for research has begun. The Lacks family would probably disagree with this argument, since their experience with a cell “abduction” has led to neglect, withholding of information, and a dehumanization resulting from lack of credit and recognition given to Henrietta Lacks. Despite all of the grievances and injustices, the Lacks cannot deny the scientific uses and progress enabled by the cells; one can only wonder what would have become of medical research if the HeLa line had not been
What could not have possibly been imagined was how this could ultimately affect the family of Henrietta Lacks. HeLa cells were unlike any other cells. They grew in mass quantities, and continued to multiply and grow in culture whereas other human cells stopped. This eventually lead to interest in the Lacks family and their genetics. Some family members were afraid for their medical health and what would happen to their genetic material if they went to the doctor.
She had so many blood transfusions that the doctors had to cut her off. Henrietta could not fight off the cancer forever and eventually passed away, and after her death nobody told her children as diseases like this were not spoken openly within families, so the children did not know about the mysterious disappearance of there mother for
Just about everyone was profiting from HeLa cells except her own family. Throughout the book we can follow the interesting stories of Henrietta’s children and the scientist who worked with HeLa cells. Many ethical questions were raised and we can engage in the argument that the author poses. Is consent from patients’ necessary to proceed with testing on patients who are unaware of the procedures being done on them?
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
The media and scientific community are guilty of viewing Henrietta Lacks and her family as abstractions. Nonetheless, the central argument of the book is that the scientific community has an ethical obligation to respect the dignity, autonomy, and person-hood of all subjects and individuals with whom it comes into contact. Accordingly, individuals cannot be made into subjects of scientific inquiry without their consent. And, when objects of scientific study (including, for example, the physical material scientists use within a laboratory setting) are sourced from individual people, those individuals deserve to be made aware of such sourcing, and when possible they ought to be appropriately compensated. Therefore, you can see how the scientific
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.
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.
In 1951, at the age of 31 Henrietta Lacks was diagnosed with cervical cancer. Henrietta was under treatment at Johns Hopkins University in Baltimore, where cells from her malignant tumor were removed. Neither Henrietta nor any of her family members knew about the tissue sample and nor did the Hopkins ever informed them of the situation. Unfortunately after Henrietta’s radiation treatment, her condition continued to worsen and soon she lost her battle to cancer on octomber 4th 1951. Henriettas cells left the Hopkins what they discovered to be known to be the first immortal human cell line.
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?
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.
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 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.
Scientists and doctors made great discoveries with the HeLa cells of Henrietta Lacks. The family of Henrietta Lacks had to live with the aftermath of decisions made by doctors and
Family, for most people, is defined as a sort of safe haven for people to go to. For others, families may be fragmented, split, or may have wrong ideals as a whole. Broken families, while they may have a long lasting effect on the spouses, can also have a detrimental, long-lasting effect on the children of these marriages which can lead to certain mental illnesses. For example, in the story of the Immortal Life of Henrietta Lacks, Deborah faces the emotional effects of her mother’s death. Other stories such as “A Rose for Emily”, show how Emily 's fathers parenting techniques and a lack of a mother figure burdened her future.