The Immortal Life of Henrietta Lacks is about the life of the woman whose cells changed the medical field and about the impact those cells have on her family. Henrietta was a black woman who grew up in Clover, Virginia in a family of poor, tobacco farmers. Her mother died when she was young and her father left shortly after, leaving her to be raised by her grandfather, who was also raising her cousin, Day. She later married Day and they moved to Turner Station, outside of Baltimore, Maryland because Day was able to get a decent paying job. Henrietta and Day had five children: Lawrence, Elsie, Sonny, Deborah, and Zakariyya. Elsie suffered from “idiocy”, which was most likely epilepsy and was committed to an asylum. When Henrietta was 31, she …show more content…
I love how she was able to gain the family’s trust and permission to tell the story. She treated the family with respect and was very open with the information she found. Many of the Lacks family members did not receive much formal education, so Skloot took time to explain the basic biology of what cells are and how Henrietta’s cells changed medicine. When Deborah or other family members incorrectly said information about HeLa cells, Skloot was quick to correct them. I do not think there was another method for Skloot to do her …show more content…
Not long after Henrietta’s round of radiation, she complained to her doctors, “that she thought the cancer was spreading, that she could feel in moving through her” and the doctors ignored her complaints (63). They told her nothing was wrong and sent her on her way. According to Skloot, that was common practice, especially during the segregation era. Patients did not question doctors because it was assumed doctors knew better and “black people didn’t question white people’s professional judgement” (63). It wasn’t until Henrietta’s forth visit in just a few weeks that they listened to her and took an X-ray of her abdomen that they found a large, inoperable
Shortly after this happened Henrietta died from the cervical cancer on October 4, 1951. It wasn’t until two decades later that Henriettas name was released to the press, and it wasn’t until even later in the 1990’s when Rebecca Skloot heard of HeLa cells and was interested why there was so little information about her. Skloot then comes into contact with Henriettas family and most importantly forms a bond with Deborah, Henrietta’s oldest daughter. This bond with Deborah was crucial to find out information of Henrietta. While researching the bond grows and Skloot realizes that Deborah just wants to learn as much as possible about her mother like she wants too (Skloot Deborah really just wants her mother’s story to be told and people to realize that there is a person behind all the
Her cell line is most commonly known as HeLa: He from the first two letters of Henrietta and La from the first two letters of Lacks. Despite this seeming positive outcome, Henrietta, specifically her family were not informed until 20 years after Henrietta's fatal cancer experience. Raising the inquiries: Was this ethical? Should the Lacks family be compensated for their mistreatment? Was the unconsented research on Henrietta lacks lawful?
Rebecca skloot, author of The Immortal Life of Henrietta Lacks, spent almost a decade gathering research in order to display Henrietta Lacks’s true story in writing. Skloot first found out about Henrietta Lack’s in her science college course at the age of sixteen. After hearing a brief description of Henrietta, with very little information, Skloot had some questions for her professor. When Skloot’s professor did not have any answers for her regarding Henrietta, she decided to take it upon herself to find out everything she could about Henrietta and her family. Skloot dedicated her life to researching Henrietta and the Lack’s family when there was no information about them.
On the topic of respect, there was also a lack of respect related to her family. The Lacks family were not all on board for the usage of HeLa cells. Infact, not until about 20 years later did the scientist have the audacity to mention it to them. When Henrietta’s children were informed that her mother's cells are still living today, they were very rudely informed. The scientists wanted more information about Henrietta, so they went to her children to collect more blood samples.
In the chapter we learned that Henrietta only had a sixth-grade education, then she started birthing her children. Most of her early life she spent time on a farm and rarely went to the doctor. After Dr. Howard Jones tested Henrietta he found a “tumor the
A main goal and component of this biography is to humanize Henrietta. Skloot aims to inform the reader about the woman behind the science; she is not Helen Lane or HeLa, but a woman who had a life and a family. Actions of the scientific community severely affected not only her, but the next generation of the Lacks family. Skloot goes on to describe her family background as well as giving an in-depth description of Henrietta herself. An element that Skloot especially emphasizes was how much Henrietta cared about her appearance: Henrietta spent hours taking care of those nails, touching up the chips and brushing on new coats of polish.
Limitations At its Finest The ability of having capacity plays an important role, especially in the medical industry, to determine if you are able to make decisions in every aspect of your life knowing that there will be consequences. A few years ago there was an African American woman whose cells were being taken and used for medical research without her consent. Rebecca Skloot who wrote, “The Immortal Life of Henrietta Lacks” in 2010, talked about this issue in the novel. The issues being told in this novel still today are being debated.
Henrietta knew it was hard to take care of a new baby and a daughter that had a baby brain. She accepted the fact that Elsie had to go to the Negro Insane for her own good. Good thing Henrietta did, as things got harder and harder for her after leaving Elsie. Last but not least the Lacks family accepted that they were never going to get money from Henrietta's cells.
She had five children when she fell ill and was devastated to learn her radium treatments left her unable to have more. She was protective of her family’s feelings, by keeping her cancer a secret from them so as not to worry them. Her family described her as an outgoing and beautiful woman of God. Henrietta and I have very little in common. I’ve never experienced prejudice because of my skin color or lived in a
Abstraction throughout history “We must not see any person as an abstraction. Instead, we must see in every person a universe with its own secrets, with its own treasures, with its own sources of anguish, and with some measures of triumph.” The Immortal Life of Henrietta Lacks explores the meaning of being an abstraction or a general idea.
Henrietta even admitted, “she, like most black patients, only went to Hopkins when she thought she had no choice,” (Skloot: 16). Henrietta felt forced to go to this certain hospital, where she was met with doctors who had no intention of explaining to her what exactly was happening to her body. Not only was she disrespected because of her financial state, her family was too. Even though their mother is the reason for the world’s largest medical revolution, strangers were given the profits that came off of Henrietta’s cells. Yet Henrietta’s children suffered so significantly, they could not even afford health insurance; for the family of the woman who created a whole new look on the medical field to
Henrietta Lacks was a black tobacco farmer from the south who, in 1950, at the age of 30, she was diagnosed with aggressive cervical cancer. Lacks went to John’s Hopkins medical center for treatment for her cancer. In April of 1951, she underwent surgery to remove the larger tumor on her cervix. Henrietta Lacks, died three days following the surgery. Even though Henrietta Lacks died, her cells from the tumor have lived on and have made a major impact on the biomedical community.
Bushra Pirzada Professor Swann Engh-302 October 4th 2015 Rhetorical Analysis: The Immortal Life of Henrietta Lacks The Immortal Life of Henrietta Lacks written by Rebecca Skloot tells the story of a woman named Henrietta Lacks who has her cervical cancer. It further goes to tell the audience how Henrietta altered medicine unknowingly. Henrietta Lacks was initially diagnosed with cervical cancer in 1951; however, the doctors at John Hopkins took sample tissues from her cervix without her permission. The sample tissues taken from Henrietta’s cervix were used to conduct scientific research as well as to develop vaccines in the suture.
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.
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.