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The immortal life of henrietta lacks summary
Discovery and experimentation with hela cells
The immortal life of henrietta lacks summary
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Did you ever wonder what are when HELA cells came to exist ?In the book the immortal life of Henrietta Lacks by Rebecca Skloot, The author answers all your questestion that you could ever have about HELA cells. In this book be theme would be injustice because the doctors took the cells form her Henrietta without her knowing because she was poor and didn’t have the money. HELA cells first came to be when Henrietta Lacks was telling a couple of her friends that she felt like she had a knot in her stomach. Five months later she had a child, but the pain in her stomach still continued, so she finally went to doctor Jones to look inside her to see if there was anything wrong. When the doctor was done with his inspection he told her that she
All I can say is amazing information of your glorious and late Henrietta Lacks. This incedible women bettered our society in ways no common human could understand at the time because of how complex this matter was and still very much indeed is. I know there is much contraversy with the matter of how scientists achived immortal cells from your late relative, and I do strongly agree with the fact that it was wrong for these researches to take advantage of this incredible women, but I know it is not for me to say nonethless it must be said that even though it was wrong to take Lacks’ cells when she was dying sometimes one must suffer to bring joy to the entire world.
An abstraction can be defined as something that only exists as an idea. People are considered abstractions when they are dehumanized, forgotten about, or segregated and discriminated against. The scientific community and the media treated Henrietta Lacks and her family as abstractions in several ways including; forgetting the person behind HeLa cells, giving sub-par health care compared to Caucasians, and not giving reparations to the Lacks family. On the other hand, Rebecca Skloot offers a different perspective that is shown throughout the book. Rebecca Skloot’s book The Immortal Life of Henrietta Lacks describes the trials and tribulations the Lacks family has gone through because of HeLa cells and shows how seeing a person as an abstraction is a dangerous thing.
In order to fully understand the significance of the life of Henrietta Lacks, one must first understand the nature of the historical moment in which she lived, and died. Henrietta Lacks was a poor, African American woman born in 1920; Henrietta lived in Clover, Virginia, on a tobacco farm maintained by many generations of relatives. This historical moment can best be understood when evaluated using a structural analysis; a structural analysis is an examination of multiple components which form an organization; structural analyses often focus on the goals and purpose of the organization in question. Henrietta and her family were greatly affected by structural violence, a type of systematic violence exerted via legislation and discrimination. Often following systematic violence is a separate type of violence, known as symbolic violence; this occurs when structural violence is viewed as normal based on media representation or popular
The Immortal life of Henrietta Lacks is a book about the women behind the scientific revolution of using actual cancer cells to perform cancer research. Henrietta Lacks was an African American woman who was barely educated and worked as a tobacco farmer. At the age of thirty she was diagnosed with cervical cancer. In Lacks’ time being uneducated, African American, and a woman was not a great mix. They were often undermined and taken advantage of. When Lacks started to become very ill she went to the nearest hospital that would accept black patients. There the doctor, George Gey, misdiagnosed her illness and took a tissue sample without her consent. After suffering through her illness and trying to keep up with her five children Henrietta died
Although she was taken from the world too soon, Henrietta Lacks was a warm hearted woman, and though unbeknownst to her, she would pave the way for the medical field and greatly expand our understanding of one of the nation’s greatest killers; cancer. In 1951 people did not talk about cancer lightly; cancer was a very touchy subject, especially for those who knew they couldn’t receive treatment once they had been diagnosed. When Lacks went to the hospital because of a “knot on her womb” she never thought that it would grow into a full fledge tumor that would end up taking her life. Henrietta lived a simple yet happy life which consisted of working on the farm, loving her husband, and raising children, and she was not going to ruin the lifestyle she knew so well by telling her family that she had cancer; it was just unheard of.
Most people live in capitalist societies where money matters a lot. Essentially, ownership is also of significance since it decides to whom the money goes. In present days, human tissues matter in the scientific field. Rebecca Skloot, author of The Immortal Life of Henrietta Lacks, shows how Henrietta Lacks’s cells have been used well, and at the same time, how they have been a hot potato in science because of the problem of the ownership. This engages readers to try to answer the question, “Should legal ownership have to be given to people?” For that answer, yes. People should be given the rights to ownership over their tissues for patients to decide if they are willing to donate their tissues or not. Reasons will be explained as follows.
In The Immortal Life of Henrietta Lacks, author Rebecca Skloot tells the true story of the woman who the famous HeLa cells originated from, and her children's lives thereafter. Skloot begins the book with a section called "A Few Words About This Book", in which a particular quote mentioned captured my attention. When Skloot began writing Henrietta's story, one of Henrietta's relatives told Skloot, "If you pretty up how people spoke and change the things they said, that's dishonest. It’s taking away their lives, their experiences, and their selves" (Skloot). After reading that quote, an array of questions entered my mind, the most important being, "Do all nonfiction authors take that idea into consideration?" Nonfiction is a very delicate and
HeLa cells were one of the greatest medical inventions that came about for the scientific field and yet the woman behind this medical feat is not fully remembered and honored. Her cells and tissue were taken away from her without consent and more than that, she was exploited for being black and not questioning what the doctor was doing. Her family suffered through countless years of agonizing pain in which they were misinformed about where and what her cells were being used for. Yes, HeLa cells changed the way we view medicine today, but only at the cost of creating one of the greatest controversies of owning ones body.
In “The Immortal Life of Henrietta Lacks,” Rebecca Skloot describes the life of an African American woman named Henrietta Lacks whose “immortal” cells changed both the field of science and her family’s lives forever. When Henrietta Lacks passed away due to cervical cancer at the young age of 31, her family accepted the fact that she was gone forever. However, little did they know that during her treatments, George Gey, a doctor at Johns Hopkins Hospital, took a sample of Henrietta’s cells and named them HeLa in hopes of finding one that multiplied infinitely. Suddenly, worldwide factories began to grow HeLa and began selling them to scientists for testing. During this process, Henrietta’s husband and 5 children had absolutely no idea that Henrietta’s cells were still alive because few knew the actual name of the patient who HeLa came from. Eventually, they found out and were furious at Johns Hopkins and refused to speak to anyone who wanted information on Henrietta. Throughout the book, Rebecca Skloot struggles
Henrietta Lacks was an african american women born on August 1, 1920, “into a family of impoverished tobacco farmers in Roanoke, Virginia” (Spigner 1).On January 29, 1951 Henrietta went to Johns Hopkins. John Hopkins was the only hospital in the area that treated black patients at that time. Henrietta went in because she felt a "knot" in her womb.She had previously told her cousins about the "knot" and they presumed that she may have been pregnant. They were correct, henrietta was indeed pregnant and she gave birth to her daughter Deborah. But after giving birth to her daughter Deborah, Lacks had a severe hemorrhage. A hemorrhage is heavy bleeding from a tissue rupture. Her primary care doctor only tested her for syphilis, which came back
The Belmont Report identifies three core principles that are to be respected when using human subjects for research. The three ethical principles are: respect for persons, beneficence and justice. In the case of Henrietta Lacks each of these fundamental components are violated. The consent that Henrietta provided was not sufficient for the procedures that were conducted.
Prior to the successful cultivation of HeLa cells, failure was met with every attempt to grow cells in culture. This roadblock became the focused work of Dr. George Gey of Johns Hopkins University. Johns Hopkins served most of the impoverished black community seeking care in the immediate Maryland area. This provided a goldmine for medical research that was justified by its “generosity” and Samaritan charter. Henrietta Lacks decision to seek care for her cervical cancer unknowingly designated her as arguably the single greatest contribution to science and medicine. After the realization that human cells had finally been successfully harvested and reproduced, Dr. Gey immediately distributed the cells and his methodology to anyone who asked. As the explosion of research on HeLa cells swept across the scientific community many of Dr. Gey's colleagues urged him to publish or patent cells to take credit for his for work but his dedication to the work rather than the credit prevented him from doing much publishing if any at all. The implica...
While doctors and scientists were making millions of dollars through HeLa research, Henrietta’s family was living in poverty. Lawrence Lacks, Henrietta’s firstborn child, says, “Hopkins say they gave them cells away, but they made millions! It’s not fair! She’s the most important person in the world and her family living in poverty. If our mother so important to science, why can’t we get health insurance?” (pg.168). Someone who disagrees with this standpoint may argue that scientists had been trying for years to develop the perfect culture medium and had a much more hands on experience with the cells (pg.35), therefore, they should be receiving the earnings from any outcomes the HeLa cells may produce. While the scientists were in fact the brains behind the scientific advances, the family should be acknowledged on behalf of Henrietta Lacks. These successes in science would not have been possible without the origin of the cells: Henrietta Lacks. For some of the family, the primary focus was not even the profit. “Since they gone ahead and taken her cells and they been so important for science, Deborah thought, least they can do is give her credit for it.” (pg. 197). Here, Deborah Lacks, Henrietta’s fourth born child, makes it clear that her primary concern is getting her mother the recognition that she deserves for her
In the novel The Immoral Life of Henrietta Lacks by Rebecca Skloot, the author tells the miraculous story of one woman’s amazing contribution to science. Henrietta Lacks unknowingly provides scientists with a biopsy capable of reproducing cells at a tremendusly fast pace. The story of Henrietta Lacks demonstrates how an individual’s rights can be effortlessly breached when it involves medical science and research. Although her cells have contributed to science in many miraculous ways, there is little known about the woman whose body they derived from. Skloot is a very gifted author whose essential writing technique divides the story into three parts so that she, Henrietta
Often in the darkest time it is good to seek relief in the good of every situation. With the death of a Mother, Daughter, and contributing member in society, it may be hard to try and find any positivity to draw from. With the unfortunate and untimely death of Henrietta, came the opportunity of life to millions of others in society then, now, and for many years to come. The goal of medical research is to put society as a whole in a better place than it was at the day before. The use of HeLa cells in every developed country on the globe has made this objective much more achievable. The Lacks family led the way for the consent form being required for patients undergoing a medical procedure Although, there was no direct benefit to the family, raising many ethical considerations that must be