Deborah also learns of her moms cells being called HeLa cells. Soon the family gets calls from the lab asking for their blood for an issue they were having with the spread of the HeLa cells. The Lacks family had no knowledge of what the cells where though or where they came from. The researchers also kept it that way cause they knew the huge amounts of profit they were making from it all. This was all bad because the way the family saw it they believed Henrietta was still alive and was being tested on in many labs and also because they have been living in poverty when what they don't know is they could be rich! Skloot the author of the book gets untangled in the story as she helps Deborah uncover the truth of her her mom and sister Elsie. They find out sad news of Elsie actually dying alone and was abused in the hospital she was in. Skloot also ends up answering the questions over their mother and how she contributed to medical research to change the…
Part two of The Immortal Life of Henrietta Lacks discusses the fate of Henrietta’s cells after she passes away. George Gey, the doctor that originally received Henrietta’s cells without her permission, asks her husband if he can perform an autopsy on Henrietta so that he can gain more knowledge on her cells. He wanted as many of her organs as possible to see if they would grow like the HeLa cells. Day refused at first because he planned on having a funeral, but Dr. Gey insisted that he perform the autopsy and promised to make her body suitable for a funeral.…
Henrietta Lacks was a beautiful, strong, independent, black woman who died of cervical cancer in 1951. She was a poor Southern tobacco farmer who worked the same land as her ancestors. She was known to be a very kind, loving, and helpful young woman. Her children, husband and cousins loved her. Everyone knew Henrietta was a very cheerful person and was always willing to help others. It all changed when she started feeling sick. She described her pain as “A knot”, she said. “It hurt something awful- when that man want to get with me, Sweet Jesus aren’t them but some pains” (The Immortal Life of Henrietta Lacks, 2010:24). On January 29, 1951, Henrietta was first taken to Johns Hopkins Hospital because of the knot she had. Johns Hopkins was her only choice fro a hospital since it was the only one near them that treated black patients. That day, Henrietta learned she had a malignant epidermis carcinoma of the cervix. But her cancer was different. Little did she know that her cancer cells would be saving lives of many others in the following years.…
I agree that patients should have rights but personally I think that scientific advancement should be prioritized. Without the HeLa and Mo cells, cures would have taken longer to develop. Though it was wrong to keep it in secrecy, if Gey and his team had not taken the cells from Henrietta the world could be very different today. If they had informed Henrietta, she could have denied them taking her cells. In addition, Chakrabarty makes an argument for his patent about an engineered bacteria, where he states “patenting cell lines didn’t require informing or getting permission from the ‘cell donors’” on page 201. Finally, Christoph’s idea of cell ownership compared to oil strengthens the science/doctor’s side.…
The Henrietta Lacks case brings up a lot of different issues, most of which have to do with ethical dilemmas. First off, Henrietta is an African American woman who came from a poor part of Virginia and was poorly educated and, unfortunately, so was most of her family. Where she grew up was mostly full of members of her family and ended up marrying her cousin, Day, now that is a heavily frowned upon in mainstream society but where she grew up it was normal. She and Day eventually moved to Baltimore, Maryland with their children. Baltimore, at the time, was heavily segregated and racism ran rampant. When she went in to John Hopkins medical center for her first treatment of her misdiagnosed cancer her doctor, without her knowledge, cut a small sliver of her tumor off and gave it to George Gey. Gey then took that sample and produced the first continuously reproducing human cell culture and culture medium to keep them going. After she had died, Gey sent an assistant to get another sliver from her corpse which ultimately failed to produce the same results, but after she had passed Day had only given permission for an autopsy. Eventually,…
This is the reason why Henrietta’s cells were immortal and kept growing. A documentary on HeLa cells and Henrietta’s contribution finally gave credit to the Lacks family. The family is still upset because they can’t even afford healthcare but their mothers cells are used everywhere. As Skloot was writing the book many people tried to prevent the family from even talking to her. Eventually Skloot gains Deborah’s trust. The stress of all that has happened in Deborah’s life causes her to become sick and she eventually has a stroke. Although The HeLa cells have led to many great contributions in the studies of viruses the book leaves the reader wondering how the family of Henrietta could have been treated so poorly considering Henrietta’s huge contribution. Henrietta’s case has also had monumental effects on laws about how patients are treated, because of Henrietta patients must give their consent rather than be tested on without their knowledge. Henrietta has had a huge role in science and for this along with her cells her contributions will live on…
Henrietta Lacks had a large, religious family who lived their entire life in poverty. She and her husband, Day, grew up together on a tobacco farm, and received little education as children. Day was a handworker and provided for the family as best he could; however, he was unfaithful to his wife on multiple occasions. Throughout their marriage, Day had affairs where he would pick up sexually transmitted infections and spread them to Henrietta. They began having children when Henrietta was only 14 years old, and they had a total of five children together. Henrietta loved her children and would have done anything for them. Their oldest daughter, Elise, had epilepsy and was nonverbal. When Elise became too much for Henrietta to handle on her own, the doctors convinced her to send Elise to Crownsville State Hospital, which was for the insane. “A bit of Henrietta died the day they sent Elise away, that losing her was worse than anything else that happened to her” (Skloot 45).…
Henrietta Lacks was born on August 1, 1920, in Roanoke, Virginia. Lacks died of cervical cancer on October 4, 1951, at age 31. Cells taken from her body without her knowledge were used to form the HeLa cell line. Lacks's case has sparked legal and ethical debates over the rights of an individual to his or her genetic material and tissue.…
Henrietta Lacks was born in 1920 in Virginia. She was a young mother of five children, three boys and two girls. After giving birth to her fourth child- Deborah- she found out that she had a “knot in her womb” and went to Johns Hopkins hospital for treatment. Back then in the 1950s, Johns Hopkins hospital was one of a few hospitals in the country because they accepted to treat black patients and the poor without payments. However, they still separated between blacks and whites. Henrietta had to go to the colored wards and enter a colored-only exam room. Her blood was labeled as colored before they stored it. In the end, when she died, her body was stored in a colored freezer. Doctor Howard Jones was…
The Immortal Life of Henrietta Lacks was about an African-American woman named Henrietta Lacks. Her cancer cells were harvested and used to create an immortal cell line for scientific experimentation. Henrietta Lacks was 30 years old at the time she went into Johns Hopkins Hospital in Baltimore in 1951. She sought help…
Problems with ethics and research have long been disputed because of the many consequences that the research could yield. For instance, the medical research in Henrietta's case has helped millions of people through the development of vaccinations and cures, however, there is an ethical dilemma. Obtaining samples from living patients without consent is unethical, yet, there is more debate when the patient is no longer alive. Perhaps the only way to alleviate problems that are similar to Henrietta’s case would be to make up for the lack of consent through compensation from the HeLa cells’ profits. Ultimately, the…
Instead it was decided that these cells would continue to be secret and the family would remain in the dark while medicine and science evolved. This is yet another prime example where informed consent is avoided and there is nothing done to correct or compensate for these tissues samples that were wrongly taken. We do have to keep in mind that up to this point the family was in the complete dark and ultimately being taken advantage of. The Lacks were a low class, poor family, there were also African-American and had very little knowledge about ethics or even consent. These researches never planned to tell the Lack family about He-La cells and I believe that they used race to their advantage.…
The author creates interest by saying how she first found out about Henrietta and she wanted to find out more information about her. My reaction on Deborah is that the way she acting is alright because she deserves to know everything that has happened to her mother. The term “Jim Crow era” is talking about the time period where the only major hospital also treated black patients. My impression on Henrietta is very surprising because of how many siblings she has, the age she got pregnant, and the other experiences she has gone through in so far. I believe that TeLinde’s research was important by him trying to find out what she had and not really justified because she didn’t know her cells were going to be given to someone else as well. Dr. Gey…
Throughout the book Rebecca Skloot shifts back and forth from Henrietta’s history to scientific research to her personal experience. In chapter ten, she gives readers a clear view of what she was seeing when she visited Clover. She describes how “dead” it appears and how things in the town are “suffering.” When she makes her way to Lackstown, she meets one of Henrietta’s Cousins named Cootie. She gets into his background, and the theme of pain and suffering is present again. Cootie says “she been gone so long, even her memory pretty much dead now. Everything about Henrietta dead except them cells.” It shows about the Lacks family that even though they face death and hardships on every side, they don’t give up. Henrietta still took care of everyone, and Cootie still built his house. When Cootie was talking, he had the radio on and a preacher was talking in the background. Cootie was saying that Henrietta’s cells were voodoo; they were either man-made or spirit-made. He talked about spirits that he’s seen and how they have protected him. Then, he relates it all back to the cells, saying that something was over them, because they weren’t any regular cells.…
The first part of Skloot’s book depicting Henrietta’s life was extremely interesting and intriguing. I was impressed by the work that Skloot went through in simply researching and learning more about Lack’s history. The amount of people talked to, documents studied, and research performed by her was amazing. The first person accounts of Lack’s life made her story really come alive. I was deeply impacted by the quality person Henrietta was. Despite poverty, racism, and illness, she had an upbeat attitude and positive outlook on life. Her circumstances would have made it easy and excusable for her to complain, but she stayed strong and determined for her family. I can’t imagine how hard it was for her to say good-bye to her children, especially her daughter Elsie. It also struck me how genuinely friendly and caring she seemed with everyone she came in contact with. Her house always had an open door and warm meal on the table. It’s not often that you meet a person with that large of a heart.…