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Physician Assisted Suicide: Palliative Care

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Physician Assisted Suicide: Palliative Care
Thesis: When it comes to the topic of physician-assisted suicide (PAS), some experts believe that an individual should have the option of ending their life in the event that they have been given six months to live with a terminal illness or when the quality of their life has been vastly changed. Where this argument usually ends, however, is on the question whether physician-assisted suicide is medically ethical, would be overly abused to the point where doctors might start killing patients without their consent. Whereas some experts are convinced that just improving palliative care would decrease the need for someone to want to end their life before it happened naturally.

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I. Introduction …show more content…

In his book Euthanasia and Physician-Assisted Suicide: Killing or Caring? Dr. Michael Manning M.D breaks euthanasia into further subsets: voluntary active euthanasia, involuntary active euthanasia, passive euthanasia and physician-assisted suicide. He states that the debate between euthanasia and physician assisted suicide can be defined as such: “Is it morally acceptable, and so ought it be legally permissible, for a physician to take the life of a competent, terminally ill patient who requests it, or for a physician to assist the competent, terminally ill patient in taking his or her own life” (4). The Oregon Legal Glossary website defines a terminal illness as “an incurable and irreversible disease that has been medically confirmed and will, within reasonable medical judgment, produce death within six months”. Some might wonder why an individual diagnosed with a terminal illness would want to hasten their time of death instead of using the time they have left to be with their family and do what they had always wanted to do. The answer to this can be traced to the ancient Greeks. Manning, notes that during classical Greek antiquity and before the Christian era of the Roman Empire, euthanasia did not mean what it means today. For the individuals of this era, euthanasia was “focused not on the act of hastening death itself, but rather on the manner of one’s …show more content…

One of the key aspects of palliative care and sometimes the key aspect in the physician-assisted suicide debate is physical independence and pain management. “Since interest in physician-assisted suicide and euthanasia resurfaced in the late 20th century, pain and physical disability have been perhaps the most frequently cited justifications for legalization of assisted suicide” (Rosenfeld 95). This concept actually leads into the discussion of quality of life. The Encyclopedia of Bioethics states that “quality of life is one of the most important but controversial issues in clinical ethics” (1388). It also cites that quality of life is used to guide medical decisions as to whether or not medical treatment should be withdrawn from a patient. Advances in medicine have made it possible for lives that would have been lost in years past can now be extended. The definition of quality of life lends itself to ambiguity and thus it takes on different meanings depending on the individual and their circumstances. If an individual was an avid cross-country runner and got diagnosis that they had a condition which would cause paralysis or if they were in an accident, would they be able to argue that their quality of life had been changed. They would go from being able to run long distances and taking care of their own needs

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