How Does Henrietta Laks Dehumanize

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.

Although she was taken from the world too soon, Henrietta Lacks was a warm hearted woman, and though unbeknownst to her, she would pave the way for the medical field and greatly expand our understanding of one of the nation’s

Have you ever been bullied or even discriminated against? Imagine that feeling of embarrassment, shame, and self-consciousness. Although I never have experienced the type of discrimination that Henrietta did, I still understand how it feels whenever you feel cheated because of another's actions and the pain that comes with self-doubt as a affect from the society. Seeing how I am affected by discrimination, it is easy to see that the theme of discrimination in "The Immortal Life of Henrietta Lacks" is relevant in today's world.

Henrietta Lacks died in 1951 of cervical cancer, leaving behind a husband, five children and some cells taken from her without her permission. These cells continue to revolutionize the scientific field today and have played an integral role in some of the most important advances in medicine: cloning, chemotherapy, gene mapping, the polio vaccine and in vitro fertilization. The Immortal Life of Henrietta Lacks answers a lot of questions regarding the Lacks family, but also poses a number of questions regarding ethics, consent and how far society is willing to go to make medical advances.

The scientific community’s careless mistreatment of the Lacks family began with dehumanizing Henrietta’s cells in the very first lab. Generalizing people can especially be easy when one is working with their cells in a lab. The many scientists working on Henrietta’s cells must have found it easy to separate the cells from the person and reduce them to tools to aid them in the task at hand. This view may be harmless when it comes to the individual scientist, and the individual cell, but this view extended to the entire Lacks family and caused them much harm. “Meanwhile, Victor McKusick and Susan Hsu had just published the results of their research in

Henrietta Lacks, a woman whose cells have made millions of dollars, but most people don’t know her name, or her story. “She’s usually identified as Helen Lane, but often she has no name at all. She’s simply called HeLa, the code name given to the world’s first immortal human cells – her cells cut from her cervix just months before she died. Her real name is Henrietta Lacks,” (Skloot 1). Through the last few months of her life, she had major struggles with hospitals and scientists. Henrietta was in serious pain throughout the last few months, and the doctor treated her as a specimen. “Henrietta is still a miserable specimen,” (Skloot 66). Another major flaw in Henrietta story is the fact that her family was barely told of her condition of cervical

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.

The non-fiction book The Immortal Life of Henrietta Lacks, written by Rebecca Skloot, details the happenings and life of Henrietta Lacks, an African American woman and tobacco farmer who became a medical miracle in the 1950’s. The book is written in an attempt to chronicle both the experiences and tribulations of Henrietta Lacks and her family, as well as the events that led to, and resulted from, research done on Henrietta Lacks’ cells. Henrietta was a very average African American woman in this period; she had only a seventh-grade level education, and followed traditional racial and gender roles by spending her time has a mother and caretaker, as well as working on farms throughout her life until the involvement of the US in World War II brought her and her husband, “Day” Lacks, comparatively better work opportunities in industrial steel mills. However, after her death in 1951 Henrietta became much more than average to doctors at John Hopkins when the discovered that cells extracted from her cancerous tissue continued to live and grow much longer than any other tissue samples. Further investigation and isolation of these thriving cells led to the creation of the first ever immortal human cell line in medical history. The incredible progress in medicine made possible by Henrietta Lack’s tissue cells were not without downfalls, though. The treatments and experiences received by Henrietta and the effects it had on her and her family demonstrate both racial and gender

While performing the treatment Dr. Lawrence Wharton Jr. collected Henrietta’s normal and cancerous cell and sent them to George Gey, who was the researcher collecting any type of cells that the hospital would provide for his research, this was all done without Henrietta’s knowledge. In the 1950’s segregating still existed, and “Many scientist believed that since patients were treated for free in the public wards, it was fair to use them as research subjects as a form of payment.” (Pg. 30) Henrietta had a painful death in 1951, due to all the tumors that had spread throughout her body, leaving her 5 children without a

The treatment of African Americans in The Immortal Life of Henrietta Lacks demonstrates the lack of ethics in the United States health care system during the 1950s and 1960s. Under the impression that medical doctors at Johns Hopkins Hospital were solely injecting radium treatment for cervical cancer, Henrietta Lacks laid on the surgical bed. During this procedure Dr. Lawrence Wharton Jr. shaved two pieces of tissue from her vagina, one from a healthy cervical tissue and one from the cancerous tumor, without Henrietta’s prior knowledge. After recovering from her surgery Henrietta exited the door marked, “Blacks Only,” the door that signified the separation between White and African-American patients. Had Henrietta been White, would the

Rebecca Skloot’s bestseller, The Immortal Life of Henrietta Lacks, begins with a quote from World War II concentration camp survivor Elie Wiesel, “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 source of anguish” (Wiesel qtd. in Skloot n. pag.). This quote serves as a preview of the book and its underlying moral purposes, as Henrietta Lacks and her family are continually treated as objects without rights to their privacy and without regards to their worth or feelings. The dehumanization of the Lacks family by the media and scientific community not only resulted in consequences for the family, but influenced society, as well.

Henrietta Lacks is woman, whose cells have been used for 63 years after her death in 1951, and will continue to be used as long as they are continue to grow. Henrietta Lacks was an African American woman who was born in the south, who married her cousin and moved up north. After giving birth to her last child, she finds that she has cancer. The doctors took a sample of her cancer cells without her permission, and now have millions of dollars but the family is still hasn’t received the money they are rightfully entitled to. Many of healthcare and entitlements that are around today, are due to the ill treatment of Henrietta and her family. Still to this day, there is very little known about Henrietta Lacks, even with the book out, and she has

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,

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

People felt oblivion when they had no clue as to what happened without their knowledge or consent. Scientists left Henrietta clueless as they took her cells from the tumor: “I’ve spent years staring at that photo, wondering what kind of life she led, what happened to her children, and what she’d think about cells from her cervix living on forever” (Skloot 1). Skloot created a feeling of sympathy by describing the mystery of Henrietta. The use of “what happened” and “what she’d think” created sympathy for Henrietta because no one knew exactly what happened to her. People deserved to have credit given where they should, and leaving them in oblivion felt unethical. The importance of Henrietta’s cells in science should result in her receiving