Hela Cells are cancerous cells that came from Henrietta Lacks tumors. Over the past 50+ years the Lacks family’s rights have been violated. The Nuremberg Code states that the voluntary consent of the human subject is absolutely essential. Without voluntary consent now is illegal but then, it was not. Not only the Lacks family was taken advantage of, but other groups of people have been taken advantage of as well. The right to having privacy has changed with new laws such as HIPAA and a few other laws within the last 60 years.
When Henrietta was taken to the John Hopkins center for a check up, they diagnosed her with cervical cancer. When Henrietta was on the examination table getting ready to go under and into surgery, not a soul told her that
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Nothing else. Them doctors never said nuthin about keepin her alive in no tubes or growin no cells. All they told me was they wanted to do a topsy see if they could help my children. And I've always just knowed this much: they is the doctor, and you got to go by what they say. I don't know as much as they do. And them doctors said if I gave them my old lady, they could use her to study that cancer and maybe help my children, my grandchildren” (Skloot 164-165). However Day did not know that they were doing this and the scientists did not care. An autopsy does not involve taking small bits from each of her organs and trying to grow her cells for personal use. Wilbur cut samples from her “bladder, bowel, uterus, kidney, vagina, ovary, appendix, liver, heart, and lungs” (Skloot 90). Gey grew Henrietta’s cells and called them HeLa cells; the immortal cells of the 50s. When a fellow researcher asked for some of the cells, Gey did not refuse to hand them over. Even though Day told Gey not to take samples they did not listen and “sold them for $25 a bottle” (Skloot 5). He did not want the Lackses family to find out what he and researchers all over the world had done, “they would’ve learned that Henrietta’s cells were still alive, that they’d been taken, bought, sold, and used in research without Hennie’s …show more content…
Prisoners were tested on, “prisoners nationwide were being used for research of all kinds - from testing chemical warfare agents to determining how x-raying testicles affected sperm count” (Skloot 129). Some of the prisoners volunteered to be used as a test subject while many others did not. Southam injected cancerous cells into more than 600 people, mostly cancer patients to begin with, and proceeding with healthy patients to see if it would make a difference; “Since people with cancer seemed to reject the cells more slowly than the healthy people did, he thought that by timing the reaction rate, he might be able to find undiagnosed cases of cancer” (Skloot 130). However, the healthy patients were not aware of what Southam was injecting into their bodies, if the patients were to ask about what he was doing to them, he would say that he was testing them for cancer but in all reality he was injecting cancer into their bodies. The patients that were test subjects were of a variety of diseases and disorders, “one person had advanced Parkinson’s and couldn’t talk, others only spoke yiddish, one had ‘multiple sclerosis’ and ‘depressive psychosis’. Regardless, Hyman wrote, ‘I was informed that consent was not necessary… that it was unlikely that Jewish patients would agree to live cancer cell injections” (Skloot 133). This would not be the only time that Jews were
The Immortal Life of Henrietta Lacks is a novel written by Rebecca Skloot, a science reporter, depicting the lives of Henrietta Lacks’s family and their connection between them and Henrietta’s famous cancer cells “HeLa Cells”. Henrietta Lacks was diagnosed with cervical cancer in 1951 and was treated with radium and radiation therapy. During her treatment process, the tumor and other cancerous tissue that was removed from her body was sent George Gey's lab at Hopkins to be grown in test tubes all without Lacks’s consent or knowledge. The cells were successfully able to divide and give the scientific community a good supply of human cancer cells to experiment on. The Lacks’s family was never informed about the cells even when there were amazing
Dr. George Otto Gey Rebecca Skloot writes in The Life of Henrietta Lacks, part two “Death” how she was able to contact the family and describes the medical research on HeLa cells. Rebecca Skloot has a hard time getting a hold of the family since trust is a big issue. To illustrate, since Henrietta Lacks cell are legendary in the medical and science community the Lacks family been bombarded with people trying to get information about Henrietta. Because of this, Rebecca, had to first gain the trust of the family before she will be able to talk to the family. Scientist and doctor used Henrietta’s cells on animals and people to study the effects of the cancer cells and gain new knowledge.
The Lacks Family E HeLa cells were discovered over sixty years ago. HeLa cells have become the foundation to many modern vaccines and have been used in scientific research since its discovery. If one were to step into a cell culture lab anywhere in the world and open its freezers, there would be millions of HeLa cells in small vials behind its doors. As much of a remarkable discovery as they may be, many fail to recognize their origin. HeLa cells were not a creation made by man in a lab, but a discovery found inside a woman.
People did not know the truth about HeLa because Hopkins hospital hid the fact that they took living samples of Henrietta’s cells without consent. “-Add quote-“they did it to continue and advance in their research. From HeLa the scientific world was booming with questions. “–Add quote-“they asked questions such as where was HeLa from and who’s the patient was with the cells. Not to mention Hopkins did not release Henrietta name because they did not want people to find out who she really was.
Hela cells. Not necessarily the cells themselves has changed anything, but the person they were taken from; Henrietta Lacks, an African-American woman whom was born August 1, 1920. Before passing on October 4, 1951, Henrietta approached Johns Hopkins Hospital in Baltimore, trying to find out what was bringing her awful abnormal pains and abdominal bleeding: soon after she was diagnosed with Cervical Cancer and treated with radium and x-ray therapy. During one particular visit tissue samples were taken from Henrietta while being ‘treated’ for her cancer and studied. Rebecca Skloot wrote, The Immortal Life of Henrietta Lacks, bringing to light the ‘complex social issues’ and ‘ethical dilemmas’ that entwined with HeLa cells and medical research.
According to Rebecca Skloot, an award winning writer most famous for her novel on Henrietta Lacks “the immortal life of Henrietta lacks”, Henrietta received “top of the line’ treatment. Although given standard treatment by no means was it enjoyable, Henrietta went through many days of terrible pain, due to the severity and nature of the procedure they performed on her, her cervix were filled with in order to try and shrink the size of the tumor. Evidently this procedure
They didn’t grow the HeLa cells for a good cause. I think that it was good that journalists wanted to find out the real woman behind HeLa cells and wanting to contacting the family. The public and Henrietta’s family should have the right to know that Henrietta is the woman whose cells have changed the world. When Henrietta had passed away, her children were sent away to live with Ethel and Galen. Joe received such great abuse from Ethel.
Maybe figure out how to duplicate the cells and use it for other drugs that can help people heal better. All through this research and testing Henrietta was left in the dark she didn’t even know that the doctors removed a piece of her cervix for research purposes. She didn’t even receive credit for her cells until much much later. No one knew about the HeLa cells except for the doctors because they were trying to keep it a secret so their project wouldn’t get shutdown by not informing the patient that they’re using their cells. Some would say that the doctors did the right thing and kept the identity of the cells disclosed because later on it led to saving so many lives.
These cells later made their way across the country and in the laboratory of Dr. George Otto Gey, who realized that there was something unusual about the cells, after conducting more tests he started to wonder why the cells weren't dying. Normal cells usually die in 2-3 days but these cells were more durable Gey multiplied the cells creating a cell line that would later travel across
I believe that the family members should have a say whether or not they have ownership of the cells. Henrietta Lacks’ consent was taken away from her, and so the next best case is to allow the family members to decide whether or not they give consent to the HeLa cells. Similar to the rule-utilitarian, if we were to disregard this case of informed consent, then what’s not to say we can violate someone else’s informed consent for another justifiable reason? This would lead to a slippery slope that could increase the lack of informed consents for patients. However, I, at the same time, understand that this is a very unique case and the cells are doing much more good than harm.
They fought and did not always get along, but one thing is for certain, family came first to them. Their importance of family shined through when Henrietta was first diagnosed with Cervical cancer. Although they were mostly uneducated, they asked questions and took the time to try to understand the disease Henrietta was diagnosed with. They were there for one another during the most difficult time of their lives. When a family member becomes ill, the rest of the family becomes your rock and shoulder to lean on.
George Gey felt that her cells were immune to these deadly diseases and this caused them to reproduce instead of dying off. Henrietta struggled most of her life with these diseases primarily because they were not vaccines at this time. In the article “ The Immortal Life of Henrietta Lacks” Ahmad explains “ HeLa cells were vital for developing the pool vaccine and uncovering secrets of cancer.” If it were not for her cells, then we would not have nearly as many vaccines as we do
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?
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.