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Book review: ‘The Immortal Life of Henrietta Lacks’ (by Rebecca Skloot)
A. Duckers
I6056150
AR&V II
Maastricht University
28-05-2014
Introduction
‘The Immortal Life of Henrietta Lacks’ is an interesting book for a broad audience. It combines scientific history with the beautiful and tragic story of Henrietta Lacks and her family. Because of its wide range, it would be best to publish this review in a magazine or newspaper that is read by a broad, higher educated audience, since they would be most interested in the story of Henrietta. Dutch examples of magazines in which a book review like this one could be published are Elsevier or Quest. International examples would be the New York Times or the Sunday Times.
Core argument
‘The immortal life of Henrietta Lacks’ is about a black woman who died in 1951. Her cancerous cervix cells, taken without her knowledge by a doctor at John Hopkins Hospital, were the first ‘immortal cells’, meaning they could be cultured in a lab. Her cell line, named HeLa (after Henrietta Lacks), then became one of the most important tools in medicine. However, this book not only focusses on the scientific story of HeLa cells, but also on the story of the woman behind the cells. It consists of three storylines, which will all be described below.
Henrietta Lacks
Henrietta was born into a poor, black family. Her father was a tobacco famer and Henrietta never really knew her mother, since she was four years old when her mother died. After her mother’s death, Henrietta spent her childhood living with her grandfather in Clover, Virginia, in what they called the ‘home-house’. When Henrietta was fourteen, her first son Lawrence was born. Four years later, his sister Elsie followed. Elsie was ‘s...
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...uremberg Code was set up in 1947 and provided researchers with ten points to make sure their experiments were ethically accepted. However, the Nuremberg Code was a guideline and it was not legally binding. Later it became obligated for researchers to have a consent form signed, but doctors are still allowed to take tissue samples, for example during a surgery, without the patient specifically consenting them to do so.
Conclusion
Before reading this book, I had never heard of Henrietta Lacks or HeLa. I found her story very interesting. Personally, I was unaware that discrimination was still such a big issue in the 1950s and that informed consent did not yet exist in this time period. The book is very well written and also understandable for people who don’t have a background in science. The story of Henrietta is fascinating and I would recommend anyone to read it.
The book The Immortal Life of Henrietta Lacks by Rebecca Skloot is the result of years of research done by Skloot on an African American woman with cervical cancer named Henrietta Lacks. Cells from Lacks’ tumor are taken and experimented on without her knowledge. These cells, known as HeLa cells, are the first immortal human cells ever grown. The topic of HeLa cells is at the center of abundant controversial debates. Despite the fact that her cells are regarded as, “one of the most important advancements in the last hundred years” (4), little is actually known about the woman behind the cells. Skloot sets out on a mission to change this fact and share the story of the woman from whom the cells originate and her family as they deal with the effects these cells have on them.
In The Immortal Life of Henrietta Lacks, Rebecca Skloot mainly focuses on three areas, the life of Henrietta Lacks and her family, ethics in the medical and research fields, and scientific advances due to HeLa cells. Skloot integrates examples of ethical controversies regarding the HeLa cells and related topics, and sociological benefits
In the book, The Immortal Life of Henrietta Lacks, by Rebecca Skloot, the author highlights the scientific advances of HeLa cells, as well as the personal setbacks of Henrietta Lacks’ family. HeLa is a commonly used cell line in laboratories worldwide and is so often referred to as “the cell line that changed modern science”. This line of immortal cells has helped advance science in ways beyond compare. HeLa has allowed cell testing, cell cloning, and the discovery of various vaccines, including the HPV vaccine. While HeLa has done wonders in the medical field, it has caused unrepairable damage among the Lacks family.
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.
Henrietta’s cells were being inaugurated with space travel, infused into rat cells, and even being used to make infertile hens fertile again. However, these are only a few of the many accomplishments that Henrietta’s immortal cells made possible: “The National Cancer Institute was using various cells, including HeLa, to screen more than thirty thousand chemicals and plant extracts, which would yield several of today’s most widely used and effective chemotherapy drugs, including Vincristine and Taxol,”(pg.139). This example of logos from the text again shows just how important these Henrietta’s cells were to the future developments in
This section is used to demonstrate to the reader the enormous effects of her death to both her family and science. Immediately following Henrietta's death, Dr. Gey is anxious to take as many samples from her body as possible. However, he must first obtain permission from her husband for an autopsy. Henrietta's husband, Day, is tricked into giving permission. He is told the autopsy will provide test results that may help his children in the future. During the autopsy, Gey's assistant Mary Kubicek takes notice to Henrietta's painted toenails and realizes that HeLa cells belong to an actual person. She says, "they came from a live woman" (Skloot 91). A few days after the autopsy, Henrietta's body is sent from Baltimore to Clover. Henrietta is buried a few days later in an unmarked grave alongside her mother in Lacks Town. Her death is swift and little mourning is conducted by the family. By placing this section second, the reader gains insight into Henrietta's family. Her children are treated poorly and her husband is absent most of the time following her death. This section is important in understanding and gaining insight into the people closest to
The Immortal Life of Henrietta Lacks tells the story of Henrietta Lacks. In the early 1951 Henrietta discovered a hard lump on the left of the entrance of her cervix, after having unexpected vaginal bleeding. She visited the Johns Hopkins hospital in East Baltimore, which was the only hospital in their area where black patients were treated. The gynecologist, Howard Jones, indeed discovers a tumor on her cervix, which he takes a biopsy off to sent it to the lab for diagnosis. In February 1951 Henrietta was called by Dr. Jones to tell about the biopsy results: “Epidermoid carcinoma of the cervix, Stage I”, in other words, she was diagnosed with cervical cancer. Before her first radium treatment, surgeon dr. Wharton removed a sample of her cervix tumor and a sample of her healthy cervix tissue and gave this tissue to dr. George Gey, who had been trying to grow cells in his lab for years. In the meantime that Henrietta was recovering from her first treatment with radium, her cells were growing in George Gey’s lab. This all happened without the permission and the informing of Henrietta Lacks. The cells started growing in a unbelievable fast way, they doubled every 24 hours, Henrietta’s cells didn’t seem to stop growing. Henrietta’s cancer cell grew twenty times as fast as her normal healthy cells, which eventually also died a couple of days after they started growing. The first immortal human cells were grown, which was a big breakthrough in science. The HeLa cells were spread throughout the scientific world. They were used for major breakthroughs in science, for example the developing of the polio vaccine. The HeLa-cells caused a revolution in the scientific world, while Henrietta Lacks, who died Octob...
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
Rebecca Skloot’s novel, The Immortal Life of Henrietta Lacks, depicts the violation of medical ethics from the patient and researcher perspectives specifically when race, poverty, and lack of medical education are factors. The novel takes place in the southern United States in 1951. Henrietta Lacks is born in a poor rural town, Clover, but eventually moves to urban Turner Station. She was diagnosed and treated for cervical cancer at Johns Hopkins hospital where cells was unknowingly taken from her and used for scientific research. Rebecca Skloot describes this when she writes, “But first—though no one had told Henrietta that TeLinde was collecting sample or asked she wanted to be a donor—Wharton picked up a sharp knife and shaved two dime-sized pieces of tissue from Henrietta's cervix: one from her tumor, and one from the healthy cervical tissue nearby. Then he placed the samples in a glass dish” (33). The simple act of taking cells, which the physicians did not even think twice about, caused decades
The book The Immortal Life of Henrietta Lacks by Rebecca Skloot, was a nonfiction story about the life of Henrietta Lacks, who died of cervical cancer in 1951. Henrietta did not know that her doctor took a sample of her cancer cells a few months before she died. “Henrietta cells that called HeLa were the first immortal human cells ever grown in a laboratory” (Skloot 22). In fact, the cells from her cervix are the most important advances in medical research. Rebecca was interested to write this story because she was anxious with the story of HeLa cells. When she was in biology class, her professor named Donald Defler gave a lecture about cells. Defler tells the story about Henrietta Lacks and HeLa cells. However, the professor ended his lecture when he said that Henrietta Lacks was a black woman. In this book, Rebecca wants to tell the truth about the story of Henrietta Lacks during her medical process and the rights for Henrietta’s family after she died.
Imagine having a part of your body taken from you without your permission, and then having those cells that are a part of your body grow and are being processed in labs around the world and then ultimately being used for the highest of research. That is what happens to Henrietta Lacks. In the book, The Immoral Life of Henrietta Lacks, we see Henrietta Lacks and her families story unravel, the numerous hardships that they faced, and the shocking revelation that their relative cells were being used for research without her consent and theirs.
As Rebecca Scoot transport her readers in her narrative of accounts of the Immortal life of Henrietta Lacks, she delicately uncovers injustice not within one family but within a system. As she focuses in giving a voice to the Lacks, she also highlights the strength and leadership of the family matriarch of Henrietta Lacks and her cell know as HELA. Envisioning Mrs. Lacks and her family trajectory it exposes discrimination and bias on a much large scale than poorly uneducated oppress Negro or African American during 1950’s. The life of Henrietta and her family’s situation had moderate similarities of another book, The Isis Paper. The Isis Papers the keys to the Colors, by Dr. Frances Cress Welsing’s, (March 18, 1935- January 2, 2016.) In
In her autobiography, “The Life of an Ordinary Woman, Anne Ellis describes just that; the life of an ordinary woman. Ellis reveals much about her early—ordinary if you will—life during the nineteenth-century. She describes what daily life was like, living a pioneer-like lifestyle. Her memoir is ‘Ordinary’ as it is full of many occurrences that the average woman experiences. Such as taking care of her children, cleaning, cooking the—world’s greatest—meals. It also contains many themes such as dysfunctional families, insensitive men, and negligent parents that are seen in modern life. The life of Anne Ellis is relatable. Her life is relatable to modern day life, however, very different.
In December 1946, the War Crimes Tribunal at Nuremberg indicted 20 Nazi physicians and 3 administrators for their willing participation in carrying out the harmful research on unwilling human subjects. Thus, Nuremberg code was the first international code for the ethics to be followed during human subject research. It was permissible medical experiments implemented in August 1947. The code also provides few directives for clinical trials (3). Syphilis study at Tuskegee in 1974 was the most influential event that led to the HHS Policy for Protecti...