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The immortal life of henrietta lacks thesis
The immortal life of henrietta lacks thesis
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The Immortal Life of Henrietta Lacks, written by Rebecca Skloot, was published in 2010. The book is non-fiction and discusses the life of Henrietta Lacks, a woman who developed cervical cancer and passed away in 1951. Although Henrietta passed, her cancer cells remained immortal, were saved by researchers and doctors, and used for numerous studies, medicines, and cancer research. Although the subject of the book is very scientific in nature, Skloot uses very accessible language so that many people can comprehend the issues the book discusses. Skloot retrieved information for the book by spending time with Henrietta’s family, most notably Henrietta’s daughter Deborah who provided Skloot with information in her journal. Skloot also accessed photos and documents to aid in writing her first book on the life of Henrietta Lacks.
Henrietta Lacks was an African American woman from Baltimore, Maryland who was a part of the lower class and therefore was not accepted by many hospitals to treat her cervical cancer. Fortunately, Johns Hopkins offered Lacks free treatment through their public ward, even though this treatment at times may not have been the most meticulous. In January of 1951, doctors discovered the large tumor in Henrietta’s cervix. This was shortly after her daughter, Deborah, was born in 1950. Deborah never truly knew who her mother was as Henrietta passed away in October of 1951. Because the treatments and services offered by the Hopkins doctors were free for Henrietta and other patients, it was expected that their bodies and cases could be used for research and this was their payment.
With this expectation, Henrietta’s cancer cells were contracted and given to Dr. George Gey. Because of the cell’s ability to reproduce very...
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...ncer, disease, sickness, etc.). Without consent, a doctor or hospital should not be able to keep a portion of patient cells to use for their benefit, whether it is to grow them for research, or sell them off to other companies and research institutions. Being able to read one’s genome in today’s world would give doctors access to a patient’s entire genetic code. This is something a patient should have control over as their blood and their DNA is their property. Hopefully, because Skloot has raised awareness about the case of Henrietta Lacks, laws will not only be created, but strictly enforced to protect patients from having their genetic information available to the public and the medical world. This legislation requires extreme specificity and preciseness but is necessary. Only if a patient has provided consent should their bodies be used for medical research.
ILofHL Pages 56-86 Summary 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 abundantly controversial debates.
The Immortal Life of Henrietta Lacks by: Rebecca Skloot has a lot of themes, but one that is most relevant in my opinion is the racial politics of medicine. Throughout the chapters, there were examples of how Henrietta, being African American, prevented her from receiving the same treatment as the white woman sitting right next to her in the waiting room. The story begins with Henrietta going to Johns Hopkins Hospital and asking a physician to check a “knot on her womb.” Skloot describes that Henrietta had been having pain around that area for about a year, and talked about it with her family, but did not do anything until the pains got intolerable. The doctor near her house had checked if she had syphilis, but it came back negative, and he recommended her to go to John Hopkins, a known university hospital that was the only hospital in the area that would treat African American patients during the era of Jim Crow. It was a long commute, but they had no choice. Patient records detail some of her prior history and provide readers with background knowledge: Henrietta was one of ten siblings, having six or seven years of schooling, five children of her own, and a past of declining medical treatments. The odd thing was that she did not follow up on upcoming clinic visits. The tests discovered a purple lump on the cervix about the size of a nickel. Dr. Howard Jones took a sample around the tissue and sent it to the laboratory.
Henrietta Lacks, birthed Loretta Pleasant, was born on August 1, 1920 to poor African- American parents. Although she was native of Roanoke, Virginia, Henrietta spent the majority of her childhood in Clover, Virginia on the tobacco field with her grandfather and a host of cousins. As a result of the excessive “quality” time with her cousins Henrietta became attached to one in particular, David “Day” Lacks. He later fathered her first child. At the age of fourteen Henrietta conceived her first child, Lawrence Lacks. Unlike White mothers who birthed their children in hospitals; Henrietta birthed her child in her grandfather’s home-house, a four room cabin previously used as slave quarters. While White patients were certain to receive the upmost patient ca...
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...
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.
Henrietta Lacks was born on August 18, 1920 in Roanoke, Virginia. She stayed with her grandfather who also took care of her other cousins, one in particular whose name is David (Day) Lacks. As Henrietta grew up, she lived with both her Grandpa Tommy and Day and worked on his farm. Considering how Henrietta and Day were together from their childhood, it was no surprise that they started having kids and soon enough got married. As the years continued, Henrietta noticed that she kept feeling like there was a lump in her womb/cervix and discovered that there was a lump in her cervix. Soon enough, Henrietta went to Johns Hopkins Medical Center to get this check and learned that she had cervical cancer. But here is where the problem arises, Henrietta gave full consent for her cancer treatment at Hopkins, but she never gave consent for the extraction and use of her cells. During her first treatment TeLinde, the doctor treating Henrietta, removed 2 sample tissues: one from her tumor and one from healthy cervical tissue, and then proceeded to treat Henrietta, all the while no one knowing that Hopkins had obtained tissue samples from Henrietta without her consent. These samples were later handed to ...
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
Your life, like many other has probably at some point been touched by Henrietta lacks and most likely you didn’t even know it.
The novel The Immortal Life of Henrietta Lacks, by author Rebecca Skloot is about a black woman whose cells were used by doctors to study medicine without her knowledge or her permission. Rebecca Skloot first heard of Henrietta Lacks when she was 16-years-old in her college biology class. Her professor, Donald Defler, mentioned Henrietta briefly during his lesson about cells. Defler talked about how Henrietta’s cells helped scientists learn all they know about cell and cell culture today, and allowed them to develop disease-fighting drugs to combat herpes, leukemias, influenza, hemophilia and Parkinson’s disease. Although Defler did acknowledge the fact that it was Henrietta’s cells who helped change the future of medicine, all Defler added was that she was a black woman. Skloot was unsatisfied with this information and she wanted to know more about Henrietta Lacks, such as “Where was she from?... Did she know how important her cells were? Did she have any children?” (Skloot 4). The problem was, though, that no one cared to find out anything about the person whose cells were famous all over the world. Most people, in fact, did not even realize that her name was Henrietta Lacks, and not Helen Lane. All people knew about this woman was that her cancerous cells were referred to as HeLa cells. Thus, Skloot’s purpose was to inform people around the world about the life of the woman whose
The more we know about genetics and the building blocks of life the closer we get to being capable of cloning a human. The study of chromosomes and DNA strains has been going on for years. In 1990, the Unites States Government founded the Human Genome Project (HGP). This program was to research and study the estimated 80,000 human genes and determine the sequences of 3 billion DNA molecules. Knowing and being able to examine each sequence could change how humans respond to diseases, viruses, and toxins common to everyday life. With the technology of today the HGP expects to have a blueprint of all human DNA sequences by the spring of 2000. This accomplishment, even though not cloning, presents other new issues for individuals and society. For this reason the Ethical, Legal, and Social Implications (ELSI) was brought in to identify and address these issues. They operate to secure the individuals rights to those who contribute DNA samples for studies. The ELSI, being the biggest bioethics program, has to decide on important factors when an individual’s personal DNA is calculated. Such factors would include; who would have access to the information, who controls and protects the information and when to use it? Along with these concerns, the ESLI tries to prepare for the estimated impacts that genetic advances could be responsible for in the near future. The availability of such information is becoming to broad and one needs to be concerned where society is going with it.
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
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 Human Genome Project is the largest scientific endeavor undertaken since the Manhattan Project, and, as with the Manhattan Project, the completion of the Human Genome Project has brought to surface many moral and ethical issues concerning the use of the knowledge gained from the project. Although genetic tests for certain diseases have been available for 15 years (Ridley, 1999), the completion of the Human Genome Project will certainly lead to an exponential increase in the number of genetic tests available. Therefore, before genetic testing becomes a routine part of a visit to a doctor's office, the two main questions at the heart of the controversy surrounding genetic testing must be addressed: When should genetic testing be used? And who should have access to the results of genetic tests? As I intend to show, genetic tests should only be used for treatable diseases, and individuals should have the freedom to decide who has access to their test results.
In the Immortal Life of Henrietta Lacks, many characters must adjust to the face of adversity to better their
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.