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.…
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.…
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…
Even though she was not informed about the samples that were taken from her as well as her family didnt know. Its because of those samples that scienetist were able to use them to test againnst other peoples samples to find cures for deadly diseases. Eventually Henrietta’s family was informed about what was going on because they were called for samples of their blood and other mateirlas. At that point they found out about HeLla and how it works and how it was named and started becacuse of henrietta even thoun they didn ask for her consent form her or her family. But they were honored by the National foundation for Cancer Research and the Smithsonian Institution. There was a book written about Henrietta by Rebecca Skloot called “The Immortal Life of Henrietta Lacks”. There was also talk about a film based on Ms. Skloot book that was going to be developed. Henrietta’s sons and granddaughter were allowed to work on it and be co-executive producer on. There were so many ways they wanted to remeber her as well as honor her. In 2010 she was given a head stone for her unmark grave as another way to appreciate her and all that she has done form a Dr. Roland at…
The story begins by vivid background info on how Henrietta came to realize that she was ill. It is evident that she is suffering from cervical tumor- a condition that is making her feel uncomfortable throughout her life. The effective foreshadowing allows us to forecast what is likely to happen. As the story progresses, we are able to understand what Henrietta really needs. From her childhood background we are able to know what she did for a job, her best friends and her family history. It is obvious that she led a good, respectable life. Chapter three is more related to the first chapter since it presents outcomes of events that transpired during Henrietta diagnosis. The chapter…
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…
When Skloot includes segments of her personal experiences, she allows the reader to see the journey of gathering information. Having to rely on what little documentation was available to her, Skloot relied on relatives to provide the life story of Henrietta Lacks. {1} Information was gathered by “conduct[ing] multiple interviews with multiple sources to ensure accuracy” (Skloot XIV). Without including the personal experience, the reader could never see how Skloot interacted with her interviewees and the Lacks family. How countless descendants denied Skloot of an interview, or how people who knew Henrietta didn’t dare speak her story without the permission of the family. One of these encounters occurred with Courtney Speed, after Skloot found her way to Turner’s Station. {3}{5} When Skloot mentioned she was trying to get into contact them, Courtney dejectedly responded, “‘I can’t tell you anything until you got the support of the [Lacks] family. I can’t risk that’” (Skloot 73). Courtney continues, ‘“I’ll tell you everything I know…just as soon as you talk to the family and they say it’s okay. I don’t want any more problems’” (Skloot 74). With the overwhelming lack of interviewees willing to share Henrietta’s story, collecting research was no easy task for Skloot.…
Hopkins, its doctors, and researchers never thought about whether or not her cells were taken with consent or contacting her family. “ Years later, when I asked McKusick if anyone had tried to get informed consent from the Lacks family, he said, “I suspect there was no effort to explain anything in great detail.” But someone should have explained everything to them and made them aware of what was going on. Even after Henrietta’s cells were taken without consent the Lacks family deserved to know was happening with Henrietta’s cells. Susan Hsu who worked with McKusick later stated that she felt very bad because at the time no one thought that the Lacks family would not understand.…
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…
Medical researchers use laboratory-grown human cells to learn the intricacies of how cells work and test theories about the causes and treatment of diseases. The cell lines they need are “immortal”—they can grow indefinitely, be frozen for decades, divided into different batches and shared among scientists. In 1951, a scientist at Johns Hopkins Hospital in Baltimore, Maryland, created the first immortal human cell line with a tissue sample taken from a young black woman with cervical cancer. Those cells, called HeLa cells, quickly became invaluable to medical research-though their donor remained a mystery for decades. In her new book, The Immortal Life of Henrietta Lacks, journalist Rebecca Skloot tracks down the story of the source of the amazing HeLa cells, Henrietta Lacks, and documents the cell line's impact on both modern medicine and the Lacks family.…
I am Catholic so I believe in a just and fair world. In this story, it sounds far from just that. In this story, racism is still a big thing around the time this story takes place. Henrietta is a poor black woman who is treated unfairly in the Hopkins hospital due to that fact she is black. She could have possibly been saved and probably would have if she was white. Her cells were stolen and the Lacks family did not even know about until HeLa cells were on the front pages on the newspapers. I personally think that by the end of the story, the Lacks family should have been paid at least, at least a fourth of all the money that was made from Henrietta’s cells. My faith would be strongly against how this family had been treated throughout the story before any type of recognitions were given to Henrietta and not just here cells which were called HeLa cells so almost no one knew her name, even students learning about the cells in school.…
While the doctors at Hopkins were examining Henrietta, there was a chance they might have missed something that could have helped her with her condition and as a result, her tumor she noticed grew bigger. “Either her doctors had missed it during her last exam which had seemed impossible or it had grown at a terrifying rate” (Skloot 17). At the time, it could be a possibility that they ignored some of the signs that Henrietta mentioned about her condition. Due to the fact, Henrietta is an African American during the 1950s; it is hard to see if the doctors paid close attention to her symptoms due to her…
George Gey is introduced into The Immortal life of Henrietta Lacks as the head of tissue-culture research at John Hopkins hospital. He was about 52 years old when he discovered the immortality of Henrietta’s cells, and this was most likely the peak of his life, thanks to this brilliant discovery. However, he came from an interesting background. Gey was born in 1889 and grew up with his parents in Pittsburgh. He was always adventurous and liked to make do with what he had. He was always looking for new discoveries and this is what led him to find that Henrietta’s cells were, in fact, immortal.…