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Summary Of The Immortal Life Of Henrietta Lacks

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Nonfiction books can often expand ones knowledge, especially in the subject of science. In the book, The Immortal Life of Henrietta Lacks, writer of the book and journalist Rebecca Scloot finds herself looking at an image of an African American whom had a tumor growing in her body without knowledge of it. This woman in the photo, Henrietta Lacks, although her name was unknown by most scientist and teachers, helped change the face of medicine back then and even today. Henrietta Lacks started getting treatment for cervical cancer at Johns Hopkins Hospital at age 31. The physicians at the hospital cut a dime size piece of her tumor and sent it into the lab where George Gey then put it on clots of chicken blood to see if the cells would grow. …show more content…

Consent is important because what if Henrietta didn’t want her tumor to be used for research. What if she did want it to be taken out? The patient should know and agree to anything happening to his or her body. This is a controversial situation because her family has never received any compensation for this discovery or for any other uses of the HeLa cells. The family did not have any kind of insurance and had a slew of other health issues they need help with but got nothing. In an interview with Debra DeBruin, Ph.D., director of the University of Minnesota Center for Bioethics, journalist Erin McHenry questioned her about the ethical issues with the Lack’s HeLa cell case. The family never understand what all was going on. They were never told any information about what their family member was truly going through, they just knew about the cancer, completely uniformed about the HeLa cell discovery. The information on the cells was out of reach to the Lack family. It wasn’t until 2013 that the Lack’s family received some reimbursement for the Henrietta’s contribution to science when a European Molecular Biology Laboratory sequenced and published Henrietta’s genome without family …show more content…

They threw around fake names, such as Helen Larsen, to throw them off track. Her real name wasn’t told to the world until the 70s. While this can be seen as good because of patient confidentiality, they still shared all of her medical issues, which is now illegal without permission so lack of privacy was a big issue here as well once her true name really did get out. But like it was stated before, they didn’t ask her or her family for any permission of any kind to do anything. Of course some may say that these are racial issues and were not cared about by the doctors because Lack’s and her family were of the minority race, it could have easily been a mistake of

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In her work, Skloot reveals Henrietta Lacks to be an African-American woman whose cervical cells were biopsied without her consent. These cells, known as HeLa (a combination of Lacks first and last name), have since been shared among various scientists and researchers and been the framework for ground-breaking research. Unlike other works on Henrietta Lacks, Skloot set out to tell

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The Immortal Life of Henrietta Lacks overviews the story of a young black woman who dies a painful death duo to an aggressive invasive type of cervical cancer, something doctors were currently studying and developing way to combat it. Rebecca Skloot, the author, takes us to journey to see through the eyes of the Lacks family. Many would call what was done to them unfair, but as Skloot lets us know, this was common practice (and still is in many cases) during that time. The important thing was that the ignorance of who was responsible for the cells that we call “immortal,” the cells that have given us a “Rosetta stone” for medical research, is now diminish, this was especially important to the Lacks. The book focuses mainly on the story of Henrietta’s

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They were not educated so when the doctor would say something scientific they would trust every word while not even understanding what he was saying. This part of informed consent was stressed throughout the book because in today’s society most people have enough education to have a general idea what is going on when they are at the hospital about to have a procedure done, making it seem

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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?

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The Immortal Life of Henrietta Lacks is at once a biography, a work of science journalism, and a book about the interconnected topics of ethics, justice, and racism. Henrietta Lacks, an African-American woman who died from cervical cancer in 1951, was the source of the so-called HeLa cell line, which is “omnipresent” (Skloot, 2010, p. 24) in modern science. The HeLa cell line was derived from Henrietta Lacks’ cancerous tumor, which, against the wishes of Henrietta’s family was taken from her corpse and has been used for prolific and lucrative medical research for over seven decades (Skloot, 2010). Skloot (2010) described The Immortal Life of Henrietta Lacks as “a biography of both the cells and the woman they came from—someone’s daughter, wife, and mother” (pp. 25-26). While the HeLa cells are ubiquitous in research, the woman from whom they came is, at best, a footnote in biological or medical textbooks.

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The details in the author’s writing are a remark, who added: “They been doctoring me off and on ever since then.” This quote goes deeper into how these men were treated while under the researchers supervision. The people’s trust was betrayed by the people they thought would help their health. People knew that this would have

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The book The Immortal Life of Henrietta Lacks, written by Rebecca Skloot and examines the life of Henrietta Lacks and her peculiar situation with her mysterious cells. This paper will focus on chapter two in the novel and how it becomes the most important part of the book when it comes to understanding Henrietta’s life story. Chapter two is called “Clover (1920-1942)”, the chapter itself dissects the early life of Henrietta and the challenges she had growing up. In this chapter, it goes over the gender, economic, and racial obstacles that greatly impacted her. It is important to understand the socio-economic conditions that led Henrietta to be treated less than human.

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Language Arts Question 4 In the beginning of The Immortal Life of Henrietta Lacks, the author, Rebecca Skloot, stated her goal and reason of writing the book. Learning biology in college, her professor mentioned Henrietta and her cells very briefly. Fortunately, this was enough to catch Skloot’s curiosity. She desired to learn more about the woman responsible for so many scientific breakthroughs.

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In the reading of “The Immortal Life of Henrietta Lacks”, the author Rebecca Skloot makes it well known that Henrietta Lacks, while a patient at John Hopkins Hospital samples of her cells was taken from her without her or her family’s knowledge or consent. We are made aware of this on page 33 “though no one had told Henrietta that TeLinde was collecting samples or asked if she wanted to be a donor — Wharton picked up a sharp knife and shaved two dime sized pieces of tissue from Henrietta’s cervix”. As a health professional, you are violating that patients’ rights and in this case the Lacks right to privacy were violated. The way that the lacks family’s right to privacy was the fact that Henrietta’s cells often referred to as the HeLa cells

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The injustice of taking Henrietta’s cells and using them for research without her consent or of her family for that matter; until 20 years later is incomprehensible. Many believe that the history of medical ethics such as the Hippocratic Oath and complying the federal law in protecting human research and confidentiality wasn’t yet recognized. All the same, the Lacks’ family isn’t given credit or acknowledgement for what Henrietta, has contributed to science, known as the HeLa cell line. Henrietta’s

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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

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The Immortal Life of Henrietta Lacks tells the story of Henrietta, an African-American woman whose cells were used to create the first immortal human cell line. Told through the eyes of her daughter, Deborah Lacks, aided by journalist Rebecca Skloot. Deborah wanted to learn about her mother, and to understand how the unauthorized harvesting of Lacks cancerous cells in 1951 led to unprecedented medical breakthroughs, changing countless lives and the face of medicine forever. It is a story of medical arrogance and triumph, race, poverty and deep friendship between the unlikeliest people. There had been many books published about Henrietta’s cells, but nothing about Henrietta’s personality, experiences, feeling, life style etc.

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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.

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The first direct violation of ethical principles with Lacks was the breach of autonomy. During her treatment at Johns Hopkins hospital in 1951, she had been informed her diagnosis was indeed cancer. Her

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In the case of Henrietta Lacks and her family, the mistreatment of doctors and lack of informed consent defined nearly 60 years of the family’s history. Henrietta Lacks and her children had little to no information about serious medical procedures and the use of Henrietta’s cells in research. Henrietta’s cells launched a multibillion-dollar industry without her consent and doctors even took advantage of her children’s lack of education to continue their research without questions: “[Doctor] did not explain why he was having someone draw blood from Deborah… he wrote a phone number and told her to use it for making more appointments to give more blood” (188). Deborah did not have the knowledge to understand the demands or requests the doctors made of her, and the doctors did not inform her explicitly.

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