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The Process Of Dying Analysis

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Recommended: Medical ethics and euthanasia

The process of dying could vary from patient to patient. Personally, speaking when my father passed away I was stunned, I had never had someone close to me pass away. All three of my siblings handled it completely different. I can see how difficult it is for families and health care providers to determine someone’s end of life care. In “The Process of Dying” By Ben A. Rich further touches on different aspects of the process of dying ranging from legal medicine and biomedical ethics. When determining when someone has passed, many believe that there is no pulse there is no longer life, but there is a particular formulation of death along with procedures and policies. In the past decades with advancement in technology, palliative care
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An Integrative Review. JAN Journal of Advanced Nursing, 1744. Karlsson, M. B.-F. (2015). A Qualitative Metasynthesis From Nurses’ Perspective When Dealing With Ethical Dilemmas and Ethical Problems in End-of-Life Care. International Journal for Human Caring, 40-48.

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Generally speaking, humans cannot be entirely prepared for dying or the death of a close person in their life. Some people say that facing death gives a person both opportunity to grow mentally and the strength to carry on in life; however, it can be too much to handle alone. Help can be needed not only from relatives and peers, but also from the experts. Strong grieving is more than usual, but life must eventually carry on. Death can be both interesting and frightening at the same time because nobody knows what happens afterwards.

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The documentary, A Death of One’s Own, explores the end of life complexities that many terminal disease patients have to undergo in deciding on dying and dignity. It features three patients, their families, and caregivers debating the issue of physician-assisted suicide or pain relief than may speed up death. One character, Jim Witcher has ALS and knows the kind of death he is facing and wants to control its timing. Kitty Rayl is suffering from terminal cancer and wants to take advantage of her state’s Death with Dignity Act and take medication to terminate her life. Ricky Tackett, on the other hand, has liver failure and together with his family and caregiver agrees on terminal sedation to relieve his delirium and pain.

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Atul Gawande’s book, “Being Mortal: Medicine and What Matters in the End,” explores different themes such as, aging, death, and the mishandling of both aging and death by the medical profession’s. This book also addresses what it means to live well near the end of life. It is not just to survive, not just to be safe, not just to stay alive as long as the medical technology allows, but, according to the author it is about what living truly means to an individual. The author describes that the idea of “Being Mortal” developed as he watched his elderly father go through a steep decline in his health and the eventual death. He soon realized that during his medical education and training he was never taught how to help his patients with managing

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1 Outline the factors that can affect an individual’s views on death and dying •Social •Cultural •Religious •Spiritual 2 Outline the factors that can affect own views on death and dying •Emotional •Past experience •Psychological •Religious •Social •Spiritual 3 Outline how the factors relating to views on death and dying can impact on practice Current and previous professional roles and responsibilities and past; boundaries limited by legal and ethical issues; professional codes of practice - internal and national; impact of management and leadership; input from other team members and workers. 4 Define how attitudes of others may influence an individual’s choices around death and dying different models of nursing care; person-centred

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He emphasizes that it is important to focus on what we can still do, and to remain in control of our lives for as long as possible. Overall, Being Mortal is an eye-opening and thought-provoking book about the importance of end-of-life planning. It is a must-read for anyone who wants to be informed and empowered when it comes to their own care. The book provides helpful advice and guidance, as well as an understanding of the importance of having conversations about end-of-life care. By following Gawande’s advice, we can ensure that we are in control of our care and that our wishes are

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In Not Just a Death, a System Failure, author Barbara Morgan criticized the US health care system’s lack of palliative care, painful treatments, and unwillingness to face the end-of-life decision, which leads to many patients suffering the last part of their lives in discomfort. The author centers her argument on the anecdote about the dying of her late mother, who spent several months in the discomfort of intensive care until the time of her death. Moran’s point is one part valid since the treatments for serious diseases are dangerous, painful, and many times only focus on prolonging life rather than improving life. However, she neglected the fact that these treatments are optional, and patients are always open to spending the last part of their life away from the hospital. Treatments for serious diseases are known to have many side effects that deteriorate patents’ health.

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This is a part of the stage where finding recovery and answers challenge doctors and the loved ones that are suffering. In the Institute of Medicine’s critical report Dying in America, there is an idea that emphasizes the importance of making a decision for the patient that is on the stage of death. JoAnn Grif, writer of Dying in America, identifies that decisions for a patient should be made before as a living will from the patient’s own preference and decision. Letting the doctor know so it can improve communication and awareness for the individual that is on treatment, and this consent should ahead of time and planned out. Although, how soon should patients reveal a will to their doctor, some will ask.

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In “The Field of Life and Death”, Xiao Hong uses the characters’ suffering and symbolism to demonstrate the breaking of traditional male and female roles. As Howard Goldblatt mentions in the translator’s introduction, “the villages’ fatalistic attitudes and repeated mention of the four distresses (birth, old age, sickness, and death) are unquestionable” (xiii), Xiao Hong represents these distresses with the main female characters without reservation in the process of childbirth, aging, disease, and death. Through childbirth, men shrink from responsibility 1. Childbirth and responsibly 2. Old Age and 3.

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Current Issues Surrounding Death A hot topic in today’s media and in discussion is the idea of physician assisted suicide and end of life care. There are several legal, ethical, social, and political issues surrounding this idea, which makes it a controversial topic. This paper will discuss some of these issues and explore the idea of physician assisted suicide and end of life care in more detail. Physician assisted suicide is defined as, “suicide by a patient facilitated by means or information (as a drug prescription or indication of the lethal dosage) provided by a physician who is aware of how the patient intends to use such means or information (Merriam-Webster, 2015).

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“Death with dignity is a human right: to retain control until the very end and, if the quality of your life is too poor, to decide to end your suffering; the dignity comes from exercising the choice.” says Jason Barber, whose wife, Kathleen Barber, died in his arms. He had one question in mind when she died. What was he going to say if someone asked him how she died? Whether she went peacefully? He decided to tell people that his wife died in peace, without any pain or suffering.

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The possible legalization of euthanasia can cause a great disturbance in how people view life and death and the simplicity of how they would treat it. "There are many fairly severely handicapped people for whom a simple, affectionate life is possible." (Foot, p. 94) As demonstrated, the decision of terminating a person 's life is a very fragile and difficult one, emotionally and mentally. Nevertheless, it’s a choice we can make if it is passive euthanasia being expressed.

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The Death with Dignity Act has two arguments: those who believe we have the right to choose how and when we die, and those who believe we do not possess that right; that we should not interfere with the natural order of life. Every year, people across America are diagnosed with a terminal illness. For some people there is time: time to hope for a cure, time to fight the disease, time to pray for a miracle. For others however, there is very little or no time. For these patients, their death is rapidly approaching and for the vast majority of them, it will be a slow and agonizing experience.

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Introduction With reference to the question posed, it has been suggested that euthanasia may be defined as “the act of intentionally causing the painless death of a sick person”. In other words, it bears the meaning of a “painless, happy or good death” as derived from the ancient Greek language – “eu”, meaning good; and “thanatos”, meaning death. Due to the rapid advancements in medical treatments, patients are capable of being kept “alive” for indefinite periods of time. Hence, in order to distinguish the ancient concept of allowing a patient to die and neglecting them treatment, the medical community has encompassed the idea of drawing a line between active euthanasia and passive euthanasia .

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The theory fails to mention the young adult patient that is dying maybe from auto collision or other incidences that subjected them to the dying stage of their life who may not have thought of making an end of life decision. The situation that put care team in a dilemma and may delay care or prolong needed care than necessary. Ruland and Moore was derived from doctoral theory course in the accumulations of empirical knowledge, clinical practice knowledge and synthesized knowledge which did not address the lower level of educators that are still scared to talk to patients about living will or who is yet to understand how to help a patient in an acute situation with a living will. Miller, B. (2017) states that physicians and nurses report discomfort in discussing end of life care with the patient from other cultures. He further expresses that the contributing factor to their inability to talk about the end of life care is lack of knowledge among practicing nurses regarding their role in educating patients (Miller,

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