In the Immortal Life of Henrietta Lacks by Rebecca Skloot, the author demonstrates the harsh realities that many African Americans faced in the medical and scientific field during the mid 20th century. The author shows the unjust practices of this time period through interviews with the Lacks family and medical professionals. These harsh realities are proven when Skloot talks to Henrietta’s family. Henrietta’s husband, Day, explains how they took samples from Henrietta’s body without consent when Skloot writes, “Day clenched his remaining three teeth. "I didn't sign no papers," he said.
In the book The Immortal Life of Henrietta Lacks Henrietta had a normal life before she found that she had cancer and everything change. Henrietta was born on August 1, 1920. When she was four years old her mom died and her father took the family back to his hometown of Clover. His father took them back to Clover so he could send his ten children to different relatives to live with them. Henrietta went to live with his grandfather and her cousin David or most people call him Day.
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.
022300 Courtney Davis Mrs. Allinder IB Literature 10 October 2016 Emotional Ties Created In The Reader Thesis: In the creative non-fiction book, The Immortal Life of Henrietta Lacks, Rebecca Skloot, creates emotional ties to the reader through the character, Deborah. Topic Sentence: Deborah was spoken about by Skloot before Deborah appeared as a live character with dialogue to form a founding idea about Deborah in the reader. Evidence: When Skloot had finally received Deborah’s number from Pattillo, Pattillo gave Skloot a list of what to do and what not to do when “dealing with” Deborah. He told her not to be aggressive or “clinical”, not to force Deborah to do anything, and definitely “don’t talk down” to her because “she hates that”.
What is the purpose of a legacy?In both stories, their legacy is changing the medical industry. Both authors carefully depicted the effect the stories will have on future generations. They expressed this by using writing styles such as, detail and imagery. “You’ve got bad blood” is a story that explains what the Tuskegee syphilis experiment was. Showing how the participants of the experiment were mistreated and lied to.
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.
Henrietta Lacks’s daughter Deborah once stated “If our mother cells done so much for medicine, how come her family can’t afford to see no doctors?” (Skloot 9). The lack of ethics also points to another theme of Henrietta’s story, discoveries are more than the discovery itself, there are always people behind them. Deborah’s words also emphasize the human side
Introduction The Immortal Life of Henrietta Lacks was an intriguing book. It not only discussed scientific thought but also other subjects as well. The book shows both the scientists point of view and the family’s point of view. In the scientists point of view the families and Henrietta’s consent was not needed.
In 1951 Henrietta omplained of a “knot in her uterus” and went to John Hopkins Hospital, a charity hospital for the poor and black, to get it checked out. Her doctor diagnosed the hard lump as cervical cancer and started radiation treatments immediately. Because of the cancer Henrietta couldn’t take care of Elsie, her oldest female child that epilepsy with her other four children. So Henrietta sent Elsie to the Crownsville State Hospital or, hospital for the negro insane until she died a little while after her mother at the age of 15. During one of her surgery’s, her doctor secretly took a slice of her tumor and gave it to Dr. George Gey, a scientist who was trying to find an “immortal cell”. Not only did Gey find what he was looking for, he found cells that grew at an abnormal rate.
Gey and Dr. TeLinde, doctors at Johns Hopkins, received a letter from Roland H. Berg, a press officer, explaining how he planned to write an article about the woman behind HeLa cells. Dr. Gey replied “I have discussed the matter with Dr. TeLinde, and he has agreed to allow this material to be presented in a popular magazine article. We must, however, withhold the name of the patient” (Skloot 106). Johns Hopkins doctors wanted to withhold Henrietta’s personal life and records, so they gave the public a fake name, Helen Lane. Doctors and other medical professionals didn’t see Henrietta as a person, instead, they saw her as a cell line and her contributions to medical advancements.
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.
Achieved Immortality A common human terror, is the fear of being forgotten. This explains the human fascination with achieving immortality, as seen in innumerable cultures throughout history. Although countless people desperately try to become immortal, only a few actually succeed, and often unintentionally, or not in the way he or she might have fancied. Such is the case of Henrietta and Deborah Lacks.
The Lacks ' Family Acknowledged But Not Compensated Henrietta Lacks was a black woman wronged of her rights and patient confidentiality in Johns Hopkins Hospital in 1951. She was a poor tobacco farmer, who after delivering her last child, Joseph, felt an unusual knot in her womb. When she thought the condition of her lump was more serious than she thought, she got it checked by Doctor Howard W. Jones at Johns Hopkins Hospital, "Jones found a lump exactly where she 'd said he would. He described it as an eroded, hard mass about the size of a nickel. If her cervix was a clock 's face, the lump was at four o 'clock," (Skloot 17).
Rebecca Skloot develops the idea that poverty comes with many difficult situations, in the book, "The Immortal Life of Henrietta Lacks". True, Henrietta and her family were poor, could barely afford their medical bills, and they didn 't get the extended care that they deserved. You will learn how being poor can change your life and what is done with it . In the book, Henrietta 's daughter, Deborah, has many medical problems and she has to spend all her money on not even all her medicine.
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.
