How would you feel if your mother’s cells changed the world of science forever? The book “The Immortal Life of Henrietta Lacks”by Rebecca Skloot is a book filled with the discoveries of medical mysteries all throughout the 1900’s.The book is about a woman named Henrietta Lacks who died due to Cervical cancer being improperly treated. Along her cancer journey, her cells were taken from her without her consent. Later, scientists came to the realization that her cells didn’t die like the average person’s did, little did they know they were dealing with something that would change the medical field forever. I will be talking about the ethics covered in the book, laws against the consent of conducting research, and the science behind it all. First, …show more content…
“They recruited hundreds of African American men with syphilis, then watched them die slow, painful, preventable deaths, even after they realized penicillin could cure them” (Skloot 50). The quote connects to my claim by talking about how when scientists were experimenting on men with syphilis to find a cure (their goal) that they continued to wait and watched them die, already knowing what could cure them, which is an example of wrong and incomplete conduct. “He repeated this process with about a dozen other cancer patients. He told them he was testing their immune systems; he said nothing about injecting them with someone else's malignant cells” (Skloot 127-128). This passage is talking about how scientists took innocent people and used them as their experiment testers without their knowledge as well as lying to them about what they were actually doing. Being in charge of medical procedures that are being done on hundreds of people is an important role to be, that being said, you should take care of your patients and give them the best possible treatments they can be provided …show more content…
“Toward the end of her treatments, Henrietta asked her doctor when she’d be better so she could have another child. Until that moment Henrietta didn't know that the treatments had left her infertile” (Skloot 47). This passage connects to my claim by showing how Henrietta's doctors didn’t tell her a crucial effect, that the tests being done would limit her ability to have children which was a very important factor to Henrietta. “The plan was that Mandel would have doctors on his staff inject 22 CDH patients with cancer cells for Southam. But when he instructed the staff to give the injections without telling the patients the contained cancer cells 3 young Jewish doctors refused, saying they wouldn’t conduct research on patients without their consent” (Skloot 130). The evidence proves that my claim is accurate by showing how some of the doctors refused to conduct research on their patients without their knowledge of what was really going to be being done to them as well as the possible outcome of the injection. In conclusion, performing research with questionable conduct being involved, on patients who are unaware or unable to question the procedure should be banned from the medical and scientific
John Moore was diagnosed with hairy-cell leukemia, a deadly cancer that filled his spleen with malignant cells. Moore had surgery to remove his spleen, and signed a consent form allowing his doctor, David Golde, to dispose of any severed tissue. Moore still kept in contact with Dr. Golde to get treatment, but without his awareness, Golde began collecting tissues and blood cells so he could market them to other doctors. Looking back at the book, “The Immortal Life of Henrietta Lacks”, it says, “They [Moore’s cells] also carried a rare virus called HTLV, a distant cousin of the HIV virus, which researchers helped to use create a vaccine that could stop the AIDS epidemic. ”(Skloot 202)
According to Rebecca Skloot, an award winning writer most famous for her novel on Henrietta Lacks “the immortal life of Henrietta lacks”, Henrietta received “top of the line’ treatment. Although given standard treatment by no means was it enjoyable, Henrietta went through many days of terrible pain, due to the severity and nature of the procedure they performed on her, her cervix were filled with in order to try and shrink the size of the tumor. Evidently this procedure
The scientific community and the media are guilty of viewing Henrietta and her family as abstractions; they did not give the Lacks family a fair trial, they’ve yet to give her family any form of compensation for the success of her cell line, and operated on Henrietta like a science fair project. In the non-fiction narrative The Immortal Life of Henrietta Lacks, written by Rebecca Skloot, it states, “The fact that no one had sued over the growth or ownership of the HeLa cell line, he said, illustrated that patients didn’t mind when doctors took their cells and turned them into commercial products.” (204) This is unfair to the Lacks family because the fraud lawyer, Keenan Kester Cofield, deceived them. Although he is a con artist, he has a wide spectrum of knowledge about law than the Lackses really have about anything; they’ve had little to no education, and they barely knew anything about the HeLa cell line.
Henrietta was just a woman seeking help to find out what she thought was a “knot” on her cervix. Going to Johns Hopkins Hospital in Baltimore Henrietta had
First of all, Henrietta was never told that many scientists were undergoing experiments on her because of her unusual cells, this was kept a secret to prevent her from ever refusing the experiments. While going through a cancer procedure a doctor Telinde who was working on her never mentioned anything about getting samples, “no one had told Henrietta that Telinde was
The Immortal Life of Henrietta Lacks is a scientific biography written by Rebecca Skloot. I usually do not find myself reading this specific type of genre, but I found myself to really enjoy this book. When I first looked at the cover, I was not expecting to learn about a woman that has changed medical research forever. The famous picture of Henrietta with her hands on her hips made her look like an average woman that may have lived to be an old age. The first chapter confirmed that my assumption was incorrect and that this book consisted of the journey of an important woman that has allowed the medical field to achieve its accomplishments.
Though these tests may be considered unethical, it is close minded thinking. Tests have to be conducted on people to provide correct information to help individuals everywhere. Whether it be injecting a child with pus, exposing the human body to different conditions, or making vaccines to incurable diseases, it has aided individuals for a better future. These tests have provided pills, shots, and a better understanding of the human body. Human experimentation has widely impacted the lives of those who are living to this
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.
Ever since a sample of Henrietta Lacks’ tissue was taken from her, without permission, the world of medicine has evolved, and multiple discoveries have been made. From the polio vaccine to figuring out how many chromosomes each human holds, HeLa cells have had some involvement. But all of this research came from a result of a violation to the medical code of ethics. The question of whether or not all research and findings that were a result of a violation of the medical code of ethics should be destroyed, has become very difficult to answer as we make more and more advances in the medical field. Personally, I believe that the way Henrietta’s cells were collected was a violation, however destroying all of the findings from it would be more detrimental to society than beneficial.
Introduction The Immortal Life of Henrietta Lacks was an intriguing book. It not only discussed scientific thought but also other subjects as well. The book shows both the scientists point of view and the family’s point of view. In the scientists point of view the families and Henrietta’s consent was not needed.
Multiple times throughout the book it was mentioned that Henrietta’s biopsy took place 60 years ago and a lot of changes have been made to science and ethics. This book did a good job bringing up ethics in science and scientific achievements that have been made over the years, but in some ways it was sensationalized to get the family the recognition they feel they deserved. As a poor, black family, the Lacks’ were discriminated against. Even the medical treatments they received were often not the best treatments offered and they were often experimented on. Having the fear of being mistreated and used for experimentation made the Lacks’ even more upset about Henrietta’s death.
It is ethical for doctors and other medical professionals to perform experimental surgery. It is ethical because if people never try something, you'll never find out if it works. In the text it states,
The origination of HeLa cells, used in biomedical research for a potential cure for cancer, had made many ground breaking discoveries in science; all thanks to one woman, Mrs. Henrietta Lacks. The history of Mrs. Lacks’s contribution to these studies raised many ethical issues concerning healthcare practice. In the short film, The Way of All Flesh, we learn how these cells were revealed by direct violation of ethical principles. During the 1950s, matters regarding informed consent practices were in their beginning stages of implementation.
While what they did was not necessarily ethical, they could have been thinking it was for the better in scientific breakthroughs. With the experiment conducted on a human being rather than a lab rat, the doctors could have gathered more information to help the cause. This is minor 'could have' however, there is no guaranteeing they got the information they were searching for. "It is impossible to know all the facts about a situation" says author of Five Steps to Better Ethical Decision making, Arthur Dobrin. The doctors gathered all the information they could at the time, thus supporting the fact they may have thought ethically.
An essential part of modern society relied on trust, especially the trust of doctors and scientists. People had the right to make an informed decision about their bodies and body parts. People had a right to their body parts, both attached and cell samples collected by doctors. The actions that the medical professions made will continue to affect future generations in both positive and negative ways. In the contemporary biographical novel, the Immortal Life of Henrietta Lacks, Rebecca Skloot used logical opinions to argue about the importance of consent to reveal the lack of morality from those in the medical field which continues to persist today.