Born in 1920 Henrietta Lacks, has helped advance the world of medicine in ways that she wouldn't think were possible. In her book The Immortal Life of Henrietta Lacks, Rebecca Skloot takes us on a powerful journey about an African American women whose cells--were taken without her consent in 1951. This book tackles many issues that existed during this time, for example, racism and many ethical issues. The experiment conducted by the surgeon J. Marion Sims addresses many of the same matters that are presented in the novel written by Skloot. Both of these medical experiments performed on African American women advanced the world of medicine, but they were also seen as unethical and morally incorrect by their peers. Henrietta’s immortal life was
Rebecca Skloot, however, used a different perspective in her portrayal of Lacks. This is evident in the way in which she conducted her research and the way she wrote the book. Skloot’s book, The immortal life of Henrietta Lacks, included both the “scientific element concerns the origin and the subsequent uses of the HeLa cell line of cultured cancer cells” (Harper, 2011, p. 463) and the social and
In the novel, the immortal life of Henrietta Lacks by Rebecca Skloot. Henrietta was a young black woman of 5 children whose cancerous cells were taken out without her knowledge. Those cells later became one of the most important tools in medicine. The case of John Moore vs. Regents of the University of California has similar ethical issues as present in the novel.
If I could meet anyone and have a 30-minute conversation with them, it would be Henrietta Lacks. Henrietta Lacks is known in science because of her immortal cancer cells. Her cells, HeLa cells, were used by scientists to discover and research experiments that would be unethical on humans. Her cells played a big part in science because they helped scientists make breakthroughs in science including understanding AIDS. The important thing about Henrietta Lacks' story is the fact that her cells were taken without her permission. It was not until decades after her death in 1951 that her family became aware of HeLa cells. During the time of Henrietta's cancer treatments at Johns Hopkins Hospital, it was not seen as unethical to take DNA samples from
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
In the Immortal Life of Henrietta Lacks, Rebecca Skloot presents multiple situations that involves Henrietta Lacks and other minorities. More importantly, Skloot talks about Henrietta’s poor treatment. The author provides the similarities between Henrietta Lacks, John Moore, and Mohan Chakraborthy’s treatment. She constantly defends minorities throughout the text because they received an awful treatment. In fact, the doctors were careless with their minority patients.
Published in 2010, The Immortal Life of Henrietta Lacks by Rebecca Skloot, is a non-fiction novel that has received notable awards. An engaging biography enfolds centered around the theme that a poverty-stricken, under-educated, black woman is extremely vulnerable to the predatory actions stemming from the sexism, classism, and racism that thrives in America. Although this book was introduced to me through the course curriculum, I found reading this book to be enlightening and more inspirational due to it deriving from real events. The Immortal Life of Henrietta Lacks centers around how the science community needs to acknowledge and right this injustice that they have profited so much from.
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.
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 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
Medical science has come a long way in the last 65 years. There have been many significant medical advances, including the development of the polio vaccine, the perfection of cell culturing techniques, the advent of medical commercialization, and progress towards understanding cancer and HIV. All of this -- and much, much more -- was made possible by one woman: Henrietta Lacks. She was an African American woman born in 1920, and by the time she died of cancer in 1951, she had made no direct contributions to the world of medicine. In fact, the thing that has since brought Henrietta’s name into the medical world was the very thing that ended up killing her. All of this was made possible by what doctors discovered inside of her tumor.
The thought of being an immortal may be something that mankind can never understand or figure out, after all science can only go so far. No human has ever been an immortal, as for a human’s cells that is a different story.
The social contract of nursing is important because it reflects the nursing's code of ethics, which is to provide care to all who are in need, regardless of their cultural, social, or economic standing. The social contract exists because we rely on a guideline to continue to provide ethical care that is within our scope of practice. Unfortunately, in Rebecca Skloot’s (2010) book, “The Immortal Life of Henrietta Lacks” there were many ethical violations throughout the whole process about the Henrietta Lacks’ cells (HeLa). The author reveals the story about the life of Henrietta Lacks, an African American woman who was diagnosed with a fast-growing cervical cancer at a young age. The cells retrieved from her cervical tumor became the first immortal cell that could survive in the lab and replicate continuously without dying. Without the consent of Henrietta Lacks and her family, these cells later became key components to the development of many groundbreaking inventions such as the polio vaccine and in vitro fertilization. Therefore, the purpose of this paper is to examine the social covenant of nursing in relation to the ethical issues behind the use of the HeLa cells without the patient’s and her family’s consent.
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
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.
Ethics, in our society, are the moral principles that govern our behavior, dictating what is right from wrong. The specifics of ethics changes as values in our society change and evolve. This occurs in Rebecca Skloots book, The Immortal Life of Henrietta Lacks. One major reoccurring theme in the book is the lack of informed consent and autonomy. Fortunately, now there are safeguards which protect human rights in regard to health care and research. The Commission for the Protection of Human Subjects of Biomedical and Behavioral Research, now part of the Department of Health and Human Services, created The Belmont Report, which is one such safeguard establishing principles for all human research (USDHHS, 1979). This paper will discuss the ethical issue of informed consent within The Immortal Life of Henrietta Lacks, the disregard to parts of the Belmont Report, as well as compare the role of the nurse in charge of Henrietta’s care versus the standards of care set for modern nurses.