Yes people should have ownership and control over where and how their tissue is being used. It is my body and if you are going to take something from me, I want to know what you are going to use it for. If it is research, I want to know what type and if it is for potential medical discoveries, I want to be compensated for my “donation”. It is not just knowing that my tissues could be used for medical research. It is having a say as to where my tissue is being studied. I have personal beliefs and I don’t want my beliefs compromised just because of research. In The Immortal Life of Henrietta Lacks, it states, “it is important for donors to be able to control who has access to their tissues, because they worry that information gathered from tissue samples might be used against …show more content…
Currently there are no laws on whether or not people should be given legal ownership of, and/or control over, their tissues. What is up for discussion is consent and money related to tissue research. For some knowing how their tissues are being used is more important than the money. Consent allows the patient to decide who and where the tissues are being given to and how they are being studied. Some people have religious beliefs, which may prevent some medical institutions from using them. Others want to know that the tissue taken from them is helping others and feel that they should be compensated for the “trouble” of having the tissue removed. Tissue research is commercialized and because of that, doctors should be required to tell patients that their tissue may provide a profit. “Estimates say one human body can
Patients have no rights to samples taken from them as they become biological waste. Yet it is not necessary for doctors to obtain consent to store the same tissues that are supposed to be biological waste and use the samples for research. The lines in bioethics are blurred and there should be stricter guidelines on how research should be conducted and exactly who should benefit from. I believe the tissue donor should receive some sort of compensation because it not for said cells, the research would not exist. As with HeLa cells, without Henrietta Lacks, there would be no HeLa cells nor any
The only problem is the patient never knew that he was going to take the cells and sell them to make profit. Since the doctor took it without him knowing it and since the patient never got any money from the cells it has caused huge debate on whether or not the cells are still property of the person after they leave your body. The court in this case ruled that the patient gets control over his cells and tissues whether they can use them or not (Skloot, 2010). Then the doctor appealed saying this that when they leave your body and are in the hands of the doctor then they own the right of your cells (ANNAS, 1990). This leads to me say that I feel that the cells are each patient’s property unless them give them to some else with consent.
Brian Lykins died soon after the surgery. Brian was not the only person who received tissue from donor 58600; others also got sick or died. Some concerns related are that there is no way to regulate human remains without someone trying to make a profit. It started off as a way to advance science and help society but the greed of money took over. So because there is no regulations or policies people will do what they must to make a profit.
Should the doctors be able to have done this without her consent? Rebecca Skloot wrote the book The Immortal Life of Henrietta Lacks to talk about this in more depth. These doctors took her cells, and used them for research and
The court said doctors said researchers should disclose financial interests in patient tissues”(Skloot 205).
Patient care is based around the individual- their best interest, treatment, and health concerns. Research is based around furthering knowledge within the medical world, by testing on people, and improving lives for future patients. In Henrietta’s case, she went to John Hopkins with the plan of being treated as a patient only, and was used for research, without education or consent. Making only a small effort to relieve her pain through radiation treatment, the physicians removed cells from Henrietta’s cervix to use in later studies. There is another line blurred, as Spigner, a University of Washington professor makes a point, stating, “The life and death of Henrietta Lacks is a cautionary tale that reflects the inherent contradiction between the stated purpose of medical research to provide benefit to humankind and the reality of blatant profiteering in the name of the advancement of science” (12).
Later, when Henrietta’s genome was published, it sparked up more drama, because this too was unethical. “That is private family information,” said Jeri Lacks-Whye, Lacks’s granddaughter. “It shouldn’t have been published without our consent” (The NY Times). I believe that the continued use of the HeLa cells would have been ethical if the scientists were given permission. “It was a big moment, a hopeful moment, sitting down with the family and bringing so many years of research without consent to an end” (NBC News).
The story of Henrietta Lacks is one of great ethical weight. I believe that no one sought out the consent or permission of the use of Henrietta Lack’s cells from herself and her family because of the breakthrough that they would make in the medical field. I believe the researchers and doctors felt that by obtaining these live cells, they could be helping millions and did not really think to the extent of asking for permission. They most likely had a vision for the use of these cells and asking for the permission from the patient themselves or even their families wasn't a thought that came to mind. Furthermore, during the time period in which the medical field was in at the time of the obtaining of Henrietta’s cells, there were no laws or set
Finally, who should decide how much something like tissues is worth? Questions like these could take time to answer, time that scientific advancement doesn’t
They took them and didn’t ask.” This quote ties together much of the story behind the ethical issues surrounding these cells and the importance of informed consent, a privilege we now take for granted
From the Henrietta situation it seems that more change gave been implemented to fix this major issue. But with every situation, there are loopholes that are evident in these consents. Hoeyer and Hogle state “Absence of proper consent is currently being construed as an ‘intolerable.’ Policies enforcing the consent requirement assume that there is a universal subject, that all subjects weigh information and make “informed” choices similarly, and that they “voluntarily” participate with similar expectations” (352). The question of ethics that is raised is what rights do individuals have over their own blood, tissue and cells when it is being used in research.
Should patient consent be required to store and distribute their tissue for research? Should doctors disclose their financial interests? Would this make any difference in achieving fairness? Or is this not a matter of fairness or an ethical issue to begin with?
Who is anyone to take the right of life from someone, just because you are being selfish and have no beneficial use for your organs, when someone is dying because they need an organ of yours? I have to agree, that if organ donations did become legal, it would change the underlying meaning of organ donations, it wouldn’t be because you truly want to help people. But even if you don’t have a choice, you would still be saving someone’s life, which is heroic. We should have compassion for people, because we never know if that could be us one
However, donation involves asking ethical questions because the treatment affects not only the people in need of transplants but also the individuals who donate. The main reason why people may consider donating organs is because of the very great benefit that this can bring to others. On the other hand, some find the idea of organ donation too invasive. Those people believe that it is wrong to take organs from people. The decision to or not to donate is a moral decision.
Ronald Faison Eng-106 February 20, 2018 Professor MaryBeth Nipp Definition Argument Essay The selling of human organs under U.S law is illegal for many reasons. By having bids on life or death situations can have a negative effect on people with low to no income waiting for an organ. The only lawful procedure for someone to receive an organ transplant as of now is to be placed on a waiting list. Human organs that are sold is considered human trafficking because it is the process of selling or transferring human tissue by force (National Institute of Justice, 2007).