At this point in time, 1951, cell cultures were unable to sustain life when taken to the lab. George Gey's goals was to be the first scientist to be able to grow live human cells outside of the human body which up until HeLa, was never done before. Also, in this time era, racism was still a big issue that limited the hospitals Henrietta was able to go to. Who knows what would've happened if she didn't go to John Hopkins Hospital and they didn't take her cells. From Henrietta's biopsy she was diagnosed with cervical cancer. With that I learned that there were two different types of cervical carcinomas; invasive and non-invasive. Henrietta had non-invasive which they also called carcinoma in situ because the cancer was in its original place. This type had been possible to diagnose for only 10 years. Before Henrietta's diagnosis he had began a study to prove carcinoma in situ was just as dangerous as invasive carcinoma. When Henrietta's cells were taken to the lab, Mary Kubicek didn't thing anything of it because all previous cells had died over and over again. However, soon after the cells were growing with " mythological …show more content…
I was kind of surprised with the reaction she got from Pattillo with him being super hesitant and not really wanting anything to do with the production of the book. However, Deborah was different and gave a lot of random information that Skloot could piece together later on. With the second phone call she was informed that Deborah was instructed not to provide any more information that could help Skloot. I then realized that the Lack's family sat in the cold with the HeLa cells and never got any recognition. Another thing, with Hela being very important in the science industry many people had already tried to get in contact with the family but, with the wrong intentions. Skloot's intentions were pure however, there was no way they coulee known
While performing the treatment Dr. Lawrence Wharton Jr. collected Henrietta’s normal and cancerous cell and sent them to George Gey, who was the researcher collecting any type of cells that the hospital would provide for his research, this was all done without Henrietta’s knowledge. In the 1950’s segregating still existed, and “Many scientist believed that since patients were treated for free in the public wards, it was fair to use them as research subjects as a form of payment.” (Pg. 30) Henrietta had a painful death in 1951, due to all the tumors that had spread throughout her body, leaving her 5 children without a
Henrietta Lacks died never knowing the impact her life would have on the world of medicine. A poor, black woman living in Baltimore, Maryland in the 1950s, Henrietta was diagnosed with cervical cancer and died only nine short months after her diagnosis at the age of thirty-one. The mother of five children, Henrietta most likely died thinking her family would be her legacy. Little did she know her doctor at John Hopkins hospital, George Gey, had taken some of her cells before she died. With Henrietta’s cells, Dr. Gey was finally able to achieve a goal he had been working toward for decades – creating the first line of immortal cells (Freeman). These cells have been used for countless scientific research and have solidified Henrietta Lacks’ place
I think this book adds a lot of value to ethical, biological and scientific education. The book gives you a very good view on how the HeLa-cells were grown, but also especially on the human behind these cells, Henrietta Lacks. Not only is the story of the discovery of HeLa relevant for (scientific) biological education, but also for scientific research education in general. The book adds value to scientific education, in a way that the story of HeLa makes you realize what the importance of research ethics is and how complicated and unfair issues about human tissue used in research are. You secretly hear the voice of Rebecca Skloot through her writing, telling the world to threat the “donors” with dignity and justice by making decent agreements and laws about human tissue used in research. She shows her readers how big the
Skloot does not dismiss Gey and the lab workers as malicious villains, but rather recognizes the complexity of the story and every person involved and aims to tell their perspectives as well. Skloot fairly characterizes everyone involved, basing most of her information on their backgrounds and opinions on interviews with them. However, the majority of the book focuses on Henrietta and Deborah Lack's perspectives, so it would be difficult not to side in their favor. Henrietta and Deborah's perspectives adds an additional emotional layer to the book, making readers even more engaged and invested in the book. The emotional aspects, however, do not take away from the intellectual debate or the facts of the
Doctor George Gey, the Doctor who presided in the surgical efforts preforming the medical treatments during Henrietta’s medical observation appointments. Henrietta Lacks family should be compensated for their family members major driving initiatives derived from researching how to cure cancer because of Henrietta cell cultures. Did Henrietta realize the potency in her body to be a medical breakthrough healing social cancer endeavors more than successfully aiding Henrietta’s survival. Better than most, yet infected as she was, health activist Mary Lasker pushed an advantage for American growth to find a cure to cancer once and for all, in 1971 Mary Lasker
It clearly obvious that to George Guy- the man who discovered HeLa cells- Henrietta was the same black women she was before she died and after she died. During this period of time, there were no set laws regarding that a patient must give permission or be notified if they cells were extracted from them. Even so, being African American and a woman during this extremely racist time period there was guarantee that she would even be told or lied to, similar to the 600 African Americans who were involved in the Tuskegee syphilis experimentation who were actually lied to.
Gey found that Henrietta cells were different than the usual cells. It was never happening before when Gey found a cell that grows with mythological intensity in the lab. Usually, every cell will die or survive for a while in the lab. “However, the Henrietta’s cancer cells seemed unstoppable as long as they had food and warmth” (Skloot 65). This was the first immortal human cells that they called HeLa. This name came from the first two letters of the name Henrietta Lacks.
Finding discoveries that would greatly benefit medicine have always been difficult to achieve in cancer research. Though, everything changed on February 1, 1951, when Howard Jones discovered that Henrietta Lacks had cervical cancer. When George Gey heard of this, he took samples from Henrietta Lacks’ tumor, and found something that changed for future medical research. George Gey had noticed that Henrietta Lacks’ cancer cells was the first human cell line that could be consistently passaged. The cells were later called HeLa cells, which were named after Henrietta Lacks. Even though scientists greatly benefited from it, Henrietta Lacks, nor her family profited from it.
If Ms Skloot had not been a part of the story, the book would not have been as interesting. Ms. Skloot's inclusion to the life of the Lacks family allowed the viewers to be in her shoes. The readers were able to see through the eyes of the author, as she goes on the quest to earn the trust from the Lacks and later on show the world that Hela wasn’t just a world changing cell but a person with a family and a life. The faith healing scene in page 289 would also have felt different because Skloot's existence in the scene gave it a feeling of bond that she had made with Deborah and Gary. Some other scene that made a difference because of her presence is in chapter 6. She was so eager to connect with the Lacks family. Skloot constantly calls
This research paper is based on the findings from the book “The Immortal Life of Henrietta Lacks”. What you will read and come to know is nonfiction. I wish I could put the pictures of what I have seen and read together here for you to perhaps get a better understanding. A story based on not Henrietta’s life being that of immortality, but rather cancer cells removed from her body without her knowledge. These were the first cancer cells to reproduce outside of her body. You will come to know about Henrietta, her cancer, her cells, and her immortal life. Perhaps we can all learn to appreciate life in greater means of appreciation after reading and knowing the life and immortal afterlife of Henrietta Lacks. You will learn about a woman, who like us, had a family, and ended up not being able to truly live life to its fullest. Making us all realize just how cancer is and the amazing research that came from being able to reproduce her cells. Not just for cancer but for various other illnesses that plague so many of us. My hope is that you take away from this a better understanding of a time we do not know, for the ups and downs of science and the possibility of immortal life.
I researched George Smith Patton Jr. He was a general during World War two and mainly served in Europe. He was born on November 11, 1885 in San Gabriel California. His father George Smith Patton Sr. also had experience in the war area, he fought for the confederate army during the Civil War. After he survived the civil war he was married to Ruth Wilson. George don't have many siblings, he only had a younger sister named Anne who they called “Nita”.
Written in the early 1950’s ‘The Crucible’ by Arthur Miller is a homage to Salem 1692, where numerous villagers were accused and hanged for witchcraft. The play explores key thematic concerns of morality, religion and life. The related text ‘Homecoming’ written by Bruce Dawe in 1968 is an anti-war poem protesting Australia's involvement in the Vietnam War during the 1960s. It explores the brutal and futile nature of war, death and a collective stance against authority. Through the use of numerous literary and dramatic devices both composer’s highlight the relationship between individuals and politics and the impact of one’s choices to stress to audiences the necessity of understanding the composers point of view so one can effectively determine the nature and abuse of power.
The Immortal Life of Henrietta Lacks is a true story of a poor, Southern African-American tobacco farmer who died in 1951 at the very young age of 31 years old from cervical cancer. Little did she know that cells harvested from her tumor, which were obtained without her consent have lived on and on and became one of the most important tools in medicine today. Despite Henrietta’s story being full of legal and ethical issues, the story was one filled with success and anguish. Success for science as her cells served as advancement in medical research and development; yet was sorrowful for Henrietta and her family. This story occurred during a time of segregation in the United States, when Henrietta Lacks believed she
Henrietta Lacks is not a common household name, yet in the scientific and medical world it has become one of the most important and talked names of the century. Up until the time that this book was written, very few people knew of Henrietta Lacks and how her cells contributed to modern science, but Rebecca Skloot aimed to change this. Eventually Skloot was able to reach Henrietta’s remaining family and through them she was able to tell the story of not only the importance of the HeLa cells but also Henrietta’s life.
The effect the discovery and creation of the HeLa cells made on the science community and Henrietta’s family had a domino effect. Both had different opinions and beliefs on the matter; this led to some difficult questions asked of the family and of the medical community. Due to the new and advanced methods of experimentation, the HeLa cells made to to the field of science, the scientific community and the media failed to remember that Henrietta and her family were not abstractions but actual people. Rebecca Skloot, however, took into account the Lack’s family, she inquired both the history of the HeLa cells as well as the Lacks family, treating them as actual people with inalienable rights.