Who Is Henrietta Lack?

Elie Wiesel once stated: “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 measure of triumph.” This means that every aspect of a person is important because they all have a story to tell which is unique. They all are much more than the stories told about them. Everyone has faced challenges in their life whether it be emotionally or physically, but have also have had achievements. In the book The Immortal Life of Henrietta Lacks by Rebecca Skloot, both the scientific community and the media are guilty of having viewed Henrietta and her family as abstractions. She was an African American women from whom a scientists took cancerous cells found in the tumor located in her cervix. The cells were named HeLa and were grown to an inconceivable number and became

The main ethical issues in this case is that researches at Johns Hopkins Hospital used Henrietta’s cell in multiple researches and send her cells to other researchers around the world without her family’s consent. Moreover, the Lackes themselves were used in medical research without informed consent, and Henrietta’s medical records were release to journalists without her family knowing.

Racism is immortal just like Henrietta’s cells it will always be around. People would do anything to be the first to discover something. At the end of the day it’s all about the money. The Mississippi appendectomies and the Tuskegee experiments were similar in the way that the government forced treatment upon minorities without consent. Henrietta’s case was different than Mississippi and Tuskegee because the doctor in Johns Hopkins didn’t experiment on her actual body but on her cells without consent. Henrietta’s case the Tuskegee experiments and the Mississippi Appendectomies are all different cases in different locations but serve the same purpose which is to take advantage of poor and uneducated minorities to

The effect the discovery and creation of the HeLa cells made on the science community and Henrietta’s family had a domino effect. Both had different opinions and beliefs on the matter; this led to some difficult questions asked of the family and of the medical community. Due to the new and advanced methods of experimentation, the HeLa cells made to to the field of science, the scientific community and the media failed to remember that Henrietta and her family were not abstractions but actual people. Rebecca Skloot, however, took into account the Lack’s family, she inquired both the history of the HeLa cells as well as the Lacks family, treating them as actual people with inalienable rights.

In the year 1951, an African American woman known as Henrietta Lacks died of cervical cancer. Unknowingly, her cancerous cells would later be discovered as the first immortal human cells. These cells were then referred to as HeLa by Doctor Gey, who was a tissue expert at the Hopkins Hospital. Her cells were discovered as the first human cells without her ever knowing they had been removed from her body and cultured. Rebecca Skloot, a journalist, and author of The Immortal Life of Henrietta Lacks embarked on a journey to discover more about Henrietta Lacks’s struggle, pain, and efforts to get treatment. Henrietta nor her family members were ever told of the cultured cells, but would later find out and be very upset. They would be shocked

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

Elie Wiesel has stated “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 measure of triumph” (as cited in Skloot, 2010, p. 1). This paper will examine the many ways in which Henrietta Lacks, a relatively poor African woman whose cells were extracted from her without any consent, was viewed primarily as an abstraction rather than a person by the scientific community and the media; and the consequences that ensued as a result.

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.

The book “The Immortal Life of Henrietta Lacks” brings up a problem in society that was a serious obstacle in the field of medicine in the 1950’s. This problem is that the individual rights of a human versus the general need of humanity. The general need of humanity is much more important than the rights of a human.

Henrietta Lacks: an unknown name up until recent years. A name that had been known to the world only as HeLa; The first two letters of a name that belonged to a poor African American tobacco farmer that unknowingly changed science and life as we know it today. Her life has finally been portrayed in a very intimate story that not only does her life some justice but also transcendentally brings to mind the philosophical issues concerning medical ethics both of the past, present, and the future. In a world of constantly evolving medical advancement, science is a pivotal force that propels ideas forward. Although most will agree that the knowledge and cures found are a positive aspect, there is also a necessary evil that is involved, including

Henrietta Lacks was a “mother of five who died of cervical cancer at only thirty-one years of age” (Gabbay). When she passed away the doctors at John Hopkins asked her husband,

After her death in 1951, for six decades, Henrietta Lacks did not exist in the eyes of the society, but her cells did. How? Well, the answer is quite simple. HeLa Cells are the first immortal human cells. These cells never die and multiply every twenty-four hours. After spending 10 years to perfect her first book, author of The Immortal Life of Henrietta Lacks, Rebecca Skloot essentially captured the life, the death, and aftermath of Henrietta Lacks’ life. With controversial issues regarding science, ethics, race, and class Skloot takes us on an extraordinary journey. From the “colored” ward of Johns Hopkins Hospital in the 1950s to stark white laboratories with freezers full of HeLa cells, from Henrietta’s small, dying hometown of Clover,

The Immortal Life of Henrietta Lacks is a true story of a poor, Southern African-American tobacco farmer who died in 1951 at the very young age of 31 years old from cervical cancer. Little did she know that cells harvested from her tumor, which were obtained without her consent have lived on and on and became one of the most important tools in medicine today. Despite Henrietta’s story being full of legal and ethical issues, the story was one filled with success and anguish. Success for science as her cells served as advancement in medical research and development; yet was sorrowful for Henrietta and her family. This story occurred during a time of segregation in the United States, when Henrietta Lacks believed she

Henrietta Lacks was a poor, black woman who died of cervical cancer in the fifties. Her cells were taken from her during surgery, without her knowledge. However, back then there were no laws about informed consent and the mindset was entirely different. Researchers knew little about cells and how they function. Her immortal cells allowed researchers to have an ample amount of resources to be able to study cells and later on develop vaccines and treatments for many diseases. Even though her cells were cancerous, they still shared many basic characteristics of a normal cell, which allowed researchers to learn a lot about a cell’s basic function. Her story explains how medical research has developed and how health care has progressed over the past sixty years.

In a HIPAA-conscious society today, some of the most obvious and concerning examples of the objectification of Henrietta and her family are the inconceivable breaches of privacy. Deborah Lacks, Henrietta’s youngest daughter, originally chose to not request access to her mother’s medical records because “she was afraid of what she might find and how it might affect her” (Skloot 209). In 1985, however, Science 85 reporter Michael Gold published a book about Henrietta’s “Immortal Legacy” including extensive verbatim quotes from Henrietta’s medical records, including details about her previous medical history, diagnosis, pain, decline and death, and even autopsy (210). Skloot recounts Gold’s offenses, “No one in Henrietta’s family had ever seen those