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 …show more content…
The power that a person holds to owning one 's own body seems like common sense then and now. There were no laws specifically regarding one’s body, but soon there were ethical scenarios by famous philosophers would. For example, the case of the spare parts surgeon or involuntary organ donor by Phillipa Foot. Phillipa Foot introduced this in the 1960s, about a decade after Lacks’s death. Here is a basic summary of the scenario and the connection it has with the Henrietta Lacks’s case. The scenario starts with five patients needing organ transplants. One day, a healthy individual walks into the doctor’s office for a routine check-up, and during his check-up, everything comes out just fine. The doctor notices that he would be a perfect match for the five individuals needing organs. The doctor has the decision of harvesting the organs to save the lives of five people at the expanse of one. Should the doctor do this? No, would be the correct answer for the following reasons; one, the person may not be an organ donor and two, the doctor would be knowingly killing someone which that in itself is an unethical thing to do. This scenario can partially relate to Lacks’s case because the doctors took her cells without her consent, but by doing so, they helped save many other people’s lives. As Guido Calabresi from Yale Law School states in his article, “Do We Own Our Bodies?”:
Similarly, taking body parts from groups that traditionally have
In 1951, a poor black woman named Henrietta Lacks, made one of the greatest medical contributions ever. Her cells, which were taken from her cervical-cancer biopsy, became the first immortal human cell line. The cells are able to reproduce infinitely in a lab. Although other immortal lines have since been developed, Lacks's "HeLa" cells are the standard in labs around the world today. Together they outweigh 100 Empire State Buildings and could circle the equator three times. Science Reporter, Rebecca Skloot's wrote the book, The Immortal Life of Henrietta Lacks, which tells the story behind the woman who transformed modern medicine. Here are just a few contribution Henrietta Lacks’s cells had made for science.
Although some may argue that the doctor’s actions were unethical, there were no laws in place; hence, the doctors did not really commit a crime. On top of that, Gey was not the only doctor or researcher of that time who took cells without consent. If this is the case, should not the other uninformed patients, whose tissues or cells were removed but did not contribute to science as much as Henrietta’s did be compensated as well? Only because Henrietta Lacks’s cells resulted in a paramount discovery, many advocate for the need to repay monetarily. Additionally, the ruling that when tissues are removed from one’s body--with or without consent--any ownership of the organs disappears further highlights the lack of need to compensate financially. This controversial ruling allows a larger supply of cells to work
Her family would later find out Henrietta was misdiagnosed. Henrietta went to John Hopkins for treatment due to it being the only hospital in her area who would treat African Americans. Many doctors during this time would use the public for research without the patient’s consent, and this happened to Henrietta. Without Henrietta’s permissions, a doctor treating Henrietta’s tumor proceeded to take tissue from her cancer tumors and her healthy cervical tissue. Her tissue ended up in Gey’s lab which were named HeLa. Two days later Henrietta’s cells began growing, and soon after Gey began giving samples of HeLa to his closest colleagues (Skloot 41). Henrietta never knew of her cells growing in the lab. Unfortunately, Henrietta’s cancer began to spread throughout her body. Treatment was not working for Henrietta, and she passed away October 4th, 1951 (Skloot 86). No one knew who Henrietta was for a long time, and she lost a lot of time of receiving credit for her cells. Henrietta’s cells ended up being sold for a profit by a manufacturer. Her family did not receive anything from Henrietta’s cells being used. Henrietta’s cells helped changed the medical world. Her cells were used for creating a polio vaccine and IVF. They also helped understand HPV, HIV, and AIDs. Henrietta’s cells have done a lot for cancer research. However, Henrietta’s family suffered deeply after her death, and
Henrietta Lacks died never knowing the impact her life would have on the world of medicine. A poor, black woman living in Baltimore, Maryland in the 1950s, Henrietta was diagnosed with cervical cancer and died only nine short months after her diagnosis at the age of thirty-one. The mother of five children, Henrietta most likely died thinking her family would be her legacy. Little did she know her doctor at John Hopkins hospital, George Gey, had taken some of her cells before she died. With Henrietta’s cells, Dr. Gey was finally able to achieve a goal he had been working toward for decades – creating the first line of immortal cells (Freeman). These cells have been used for countless scientific research and have solidified Henrietta Lacks’ place
In 1951, Henrietta Lacks was diagnosed with cervical cancer at John Hopkins Hospital. Henrietta complained of a knot in her womb that caused her pain so she decided to visit the hospital in search of diagnosis. After being diagnosed with cervical cancer, the doctor recommended a biopsy be done on her cancerous tissue. Without any consent, Henrietta’s doctors took tissue samples from her cervix and attempted to grow them and keep them alive. These cells were known as HeLa cells, they began to grow at an unbelievable rate; The HeLa cell became vital for the development of vaccines and other scientific research. However because of Henrietta’s race and economic standpoint, Henrietta Lacks and the rest of the Lacks family was exploited by doctors. The exploitation of the family allowed the doctors and researchers to benefit scientifically and monetarily.
Henrietta Lacks died never knowing the amazing impact that she would have on the growth of humanity. Not only did she not know of the tissue samples that were taken from her, but her family was also unaware of the sampled cells. This came as a surprise to them, and they were understandably angry after hearing how corporations profited from cells taken from their now deceased mother, adding insult to injury. Their discontent with the use of their mother's cells was one of the first of its kind, a new ethical dilemma for a new scientific age. Although I think that the way that the scientists used the HeLa cells was warranted, The Immortal Life of Henrietta Lacks documents how far ethics in medicine has come
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 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
The Immortal Life of Henrietta Lacks is a novel written by Rabecca Skloot that outlines the life and story of a woman named Henrietta Lacks and her families struggle to discover the truth. Henrietta Lacks was and African American women who was diagnosed with cervical cancer at the age of thirty. A doctor at John Hopkins Hospital examined Henrietta and a biopsy of the cancerous tissue was retrieved. Henrietta received treatment for her cancer, but the cancer was too aggressive and she soon passed away at age of thirty-one, but her cells continue to live today. Henrietta Lack’s cells were unlike any other humans cells ever examined. The cells were able to grow, multiply, and divide outside of the human body in a lab (Skloot 2010). This was a major scientific discovery. Henrietta’s cells, more commonly known to the public as HeLa, aided in the creation of several scientific discoveries and are still used today. It is because of HeLa we have the polio vaccine, a better understanding of cancer, and cells in general. The cells have even been sent into space and have been exposed to nuclear testing and to toxins (BigPicture). Although Henrietta Lacks’s cells have done a lot good, many ethical issues surround her case such as privacy issues, monetary compensation, exploitation, and cell contamination to name a few. Perhaps the most important and controversial ethical issue in Hennrietta’s case resides around consent, or the lack there of.
In the novel, The Immortal Life of Henrietta Lacks, by Rebecca Skloot, scientists steal cancerous cells from a middle aged black woman named Henrietta Lacks without her consent. She soon passed away and her cells were then put in culture and, unlike any other cells previously, succeeded in growing and reproducing outside of the body. This new breakthrough led to a scientific revolution that changed the world as we know it. The cells, called HeLa, were mass produced in factories and distributed all around the world. They allowed scientists to conduct studies and experiments that were impossible before; consequently, numerous new discoveries and cures were made and polio was eradicated. However, Henrietta’s family had no idea what her cells did
“The Immortal life of Henrietta Lacks” written by Rebecca Skloot exposes the truth about a colored woman, Henrietta Lacks, who died from cancer leaving five children and a husband behind. Before her death doctors took her cells,without her or her family consent, to do there own research and experiments. They discovered that her cells were immortal, they became the first immortal cells known as the HeLa cells..After the discoverment the Lacks family were never told that Henrietta Lacks cells were used, bought and sold. Through the HeLa cells the scientist had made money while Henrietta kids were mistreated and were in poor situations.It wasnt till 25 years later that the Lacks family found out about the HeLa cells doing miracles. Rebecca Skloot though “The immortal Life of Henrietta Lacks” was able to explain the unethical situations that the Lacks family faced after Henrietta’s death.
Throughout the book The Immortal Life of Henrietta Lacks, many social justice issues were presented. One of them was racial discrimination, specifically in the medical world. Race was perceived in an extremely different way than it is now; it is clearly evident how it impacted the medical care that Henrietta Lacks received and what happened with the family as her cells were spread and studied. Today the situation would be handled differently. There are not segregated hospitals with people saying that since a person does not have enough money to pay for a hospital visit, taking tissues and cells from the body is okay. Racial discrimination in the medical world has changed a great deal since the time that the HeLa cells were first taken.
The cells were kept alive long enough to allow the researchers to go in depth with studies and examinations. The ethical issue was, like stated before, that the Lacks family did not give physicians permission to take samples of her cells. But during that time permission was not required and that is why they were able to take the samples. In the court case of California v. Regents of UC in 1990 it was ruled that a person’s discarded tissue was not their property and could be used. The ethical concerns are still around today because recently researchers published their results and this affected the family. Things like lack of respect for the Lacks, just and even race and social class come into the conversation because of the use of her tissue without her 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
“The Immortal Life of Henrietta Lacks” is the story of Hela cells and the women and family behind them. HeLa cells are the cells that have helped scientists all around the world discover cures and vaccines that have saved thousands of lives. But before they did all those things, they were inside a woman, named Henrietta Lacks, and were taken from her without her knowledge. Her family would not know about her cells until years after her death and millions of dollars in revenue gained from the HeLa cells. At the time doctors did what was considered common practice but did they cross a line? Or were the amazing scientific achievements enough to excuse the violation of personal privacy? Despite good intentions doctors should never have taken Henrietta’s cells without her consent, and furthermore her family deserves compensation for the work those cells have helped accomplish, and the sometimes horrible circumstances they have had to deal with because of the cells.