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Problems with euthanasia and assisted suicide
Euthanasia and physician assisted suicide
Essays on euthanasia and assisted suicide
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Choosing to sustain life artificially or to end life support is a topic that has faced, and still faces today, a lot of controversy. Many believe that life should be prolonged as there can be hope for individuals that are on life support, but other may disagree. The body is a complex system; much like a machine, there are many moving parts, signals being passed, responses being triggered, and when some of our “parts” stop functioning as they should we cease to be. The medical field can use life support systems to keep one’s essential organs running for various reasons such as assisting in the chance of survival or because it was what one’s family wanted. However, controversy arises when the patient being held alive can no longer have a say in the decisions being made and one can only speculate on what his or her wishes may be. …show more content…
A young girl undergoing a tonsillectomy at Children’s Hospital in Oakland, California, experienced blood loss and went into cardiac arrest. Jahi was originally declared brain-dead, and controversy arose, between the hospital and her family, whether to keep her alive on life support or to “pull the plug,” (Bender & Alund, 2016). Now in the case of Jahi, which is still ongoing today, it is said that she has shown signs of improvement (Shoichet, 2013). When diagnosed brain-dead, there usually is no hope for recovery, and in Jahi’s case, the state of California had printed a death certificate upon their determination of her status (Death Certificate, 2014). Jahi’s family believes there is still hope for their child and that she will wake up one day, and her signs of improvement may be proof to such hope. Keeping a patient alive on life support may be what the family wants, but also these instances can open opportunities for doctors to learn from these
In conclusion, we support the Court’s conclusion to uphold the doctor’s decision not to resuscitate Charlotte Wyatt on the grounds that she was no longer truly living and her prolonged existence and suffering did not outweigh the sum of the costs to both herself and everyone involved. Although ownership, or responsibility for a minor usually falls upon the parents or guardians, under these conditions they were unable to make an unbiased decision due to emotional investment.
Jahi McMath is a 13-year-old girl living in Oakland, CA who was declared brain dead by multiple neurologists more than three months ago. Jahi was declared brain-dead December 12th after barriers during surgery a few days earlier to remove her tonsils, adenoids, and uvula at Children's Hospital & Research Center Oakland. At least three neurologists confirmed that Jahi was unable to breathe on her own, had no blood flow to her brain, and had no sign of electrical activity in her brain. Moreover, a court order kept Jahi's body on a ventilator while independent experts could be brought in to confirm the results (Wells, 2014). Even so, the McMath family was able to secure the release of Jahi's body through the county coroner, who issued a death certificate, and have been keeping her on a ventilator at an undisclosed facility ever since. This all occurred after Children’s Hospital released Jahi due to her severe brain damage along with the probability of the hospital receiving profit from discharging Jahi before her or her family were ready for her to be released (Johnson and Rhodes, 2010, p. 61).
The decision to be able to prolong life has been one of the most controversial topic for years now. Many people believe that life support isn’t benefiting the person just only making the person live longer and others believe that it’s a chance the patients can come off life support breathing on their own which there has been many cases where patients have awakened from life support. In this exploratory essay I will talk about the 3 article that embodied their opinion about life support. In the first article Berger position on the issue is that he is against Dying patients being kept on life support because he believes once the person is critically ill which some call it brain dead there’s no coming back from
Increasingly, people know from their own experience some painful dilemmas involving elderly or handicapped individuals who are in pain. While the achievements of modern medicine have been used to prolong and enhance life for many, they have also helped create an often dreaded context for dying. Costly technology may keep persons alive, but frequently these persons are cut off from meaningful relationships with others and exist with little or no hope for recovery. Many fearfully imagine a situation at the end of their lives where they or their trusted ones will have no say in decisions about their treatment.
However, the framework in practice is very complex, and has various inconsistencies, such as the legality of refusing treatment, the sovereignty of a living will and the issue of prosecuting those who assist someone to end their lives. There is evidence that shows doctors using palliative sedation as a means to facilitate death in patients that are in extreme pain and the use of limiting or even stopping treatment at the patient’s request is not uncommon. The difficulties of putting the law into practice make it extremely difficult for courts, legislators and doctors to reach clear decisions on individual cases. Therefore, the inconsistencies in the legal framework need to be addressed, as with these present the argument against legalising the right to die is weakened. Legalising assisted dying would simplify the framework and ensure that set barriers and safeguards could be created in order to protect the patient and his/her
In an effort to provide the standard of care for such a patient the treating physicians placed Ms. Quinlan on mechanical ventilation preserving her basic life function. Ms. Quinlan’s condition persisted in a vegetative state for an extended period of time creating the ethical dilemma of quality of life, the right to choose, the right to privacy, and the end of life decision. The Quilan family believed they had their daughter’s best interests and her own personal wishes with regard to end of life treatment. The case became complicated with regard to Karen’s long-term care from the perspective of the attending physicians, the medical community, the legal community local/state/federal case law and the catholic hospital tenants. The attending physicians believed their obligation was to preserve life but feared legal action both criminal and malpractice if they instituted end of life procedures. There was prior case law to provide guidance for legal resolution of this case. The catholic hospital in New Jersey, St. Clare’s, and Vatican stated this was going down a slippery slope to legalization of euthanasia. The case continued for 11 years and 2 months with gaining national attention. The resolution was obtained following Karen’s father being granted guardianship and ultimately made decisions on Karen’s behalf regarding future medical
A divergent set of issues and opinions involving medical care for the very seriously ill patient have dogged the bioethics community for decades. While sophisticated medical technology has allowed people to live longer, it has also caused protracted death, most often to the severe detriment of individuals and their families. Ira Byock, director of palliative medicine at Dartmouth-Hitchcock Medical Center, believes too many Americans are “dying badly.” In discussing this issue, he stated, “Families cannot imagine there could be anything worse than their loved one dying, but in fact, there are things worse.” “It’s having someone you love…suffering, dying connected to machines” (CBS News, 2014). In the not distant past, the knowledge, skills, and technology were simply not available to cure, much less prolong the deaths of gravely ill people. In addition to the ethical and moral dilemmas this presents, the costs of intensive treatment often do not realize appreciable benefits. However, cost alone should not determine when care becomes “futile” as this veers medicine into an even more dangerous ethical quagmire. While preserving life with the best possible care is always good medicine, the suffering and protracted deaths caused from the continued use of futile measures benefits no one. For this reason, the determination of futility should be a joint decision between the physician, the patient, and his or her surrogate.
Terminally ill patients deserve the right to have a dignified death. These patients should not be forced to suffer and be in agony their lasting days. The terminally ill should have this choice, because it is the only way to end their excruciating pain. These patients don’t have
Once a person is brain dead they are said to be legally dead and the time and date of death is reflected on their death certificate. In South Africa it is not stated that doctors can withdraw life support once a patient is declared brain dead due to ethical debates (Fleischer, 2003). There have been some cases where people have been declared brain dead but then regain some brain activity (Greenberg, 2014). This h...
One of the many concerns is allowing incompetent individuals making this irreversible decision, which is why, “all have agreed that this end-of-life option should apply on to competent individual’s”(113). In addition, people opposed to this method argue that patients demanding this process are suffering from depression and not able to make decisions; yet, Rosenfled explains that practitioners most ensure that patients who consent to this medical intervention do it voluntarily, knowingly and
Let's begin our consideration with a nine-year-old named Ryan Atencio. He was taken off life-support systems, except for a feeding tube, after being in a vegetative state following a massive head injury in a December 10, 1988 car accident. "There was no brain function," said Dr. Eustaquio Abay at St. Francis Regional Medical Center in Witchita, Kansas. "Three or four times we'd seen the pulse go down to zero -- no circulation at all to the brain for 30 minutes on end." Yet, on January 19, 1989, Ryan squeezed his mother's hand, opened his eyes, and came back to life, so to speak (Boy).
According to a 2005 Pew Research Center Survey, American’s overwhelmingly support an individual’s right to decide whether he or she want to be kept alive through medical treatment. 84% of those polled said that they approved of laws which say medical treatment which is keeping a terminally ill patient alive can be stopped if that is what the patient desires. 70% said there are some circumstances when a patient should be allowed to die while 22% said medical personnel should do everything possible to wave the life of the patient. (Parker, 2009)
Imagine visiting your 85-year-old mother in the hospital after she has a debilitating stroke. You find out that, in order to survive, she requires a feeding tube and antibiotics to fight an infection. She once told you that no matter what happened, she wants to live. But the doctor refuses further life-sustaining treatment. When you ask why, you are told, in effect, "The time has come for your mother to die. All we will provide is comfort care."
Enabling patients with the option of medically assisted dying not only allows individuals to be entitled to a peaceful death, but it is also a desire to have suffering ended now rather than having patients living the few remaining days of more suffering and debility. Until doctors and the general public are educated, this will continue to be a controversial topic that questions values and ethics.
President's Commission for the Study of Ethical Problems in Medicine and Biomedical and Behavioral Research. Defining Death: A Report on the Medical, Legal and Ethical Issues in the Determination of Death. Washington, D.C.: U.S. Government Printing Office, 1981.