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Palliative Care: The Importance Of Palliative Care

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Recommended: Role of palliative care in dying patient

No one wants to think about palliative care, wills or living wills because we have a fear of death. A will can be one of the most important documents you ever write. If you do not have one you will not be able to select what family members you want to leave your property to. A living will, unlike a will, has no power over death and is created to express ones wishes for therapeutic treatment amid sickness. Palliative care is different from hospice because it does not only serve the dying but focuses on improving life and providing comfort for those with serious and life-threating illnesses (Kam). There can be serious consequences of dying without a will or not being able to let family know what type of medical care you wish receive if …show more content…

A will is a declaration of how a person wants their property to be distributed upon their death (Cheeseman) and can be changed throughout your life. It gives you the opportunity to provide guardians for your minor children as well as burial preferences. Without a will, someone must be appointed to act as an administrator over your estate. According to some state statues your property can be distributed to relatives and if there are no living relatives, the property escheats to the state (Cheeseman). At the end of the day if you die before you are able to write a will, you will not be able to exclude or include any beneficiaries and the fate of your family receiving your assets may be decided by the …show more content…

A living will, also known as advance directives, states which life-saving measures the signor does and does not want; can specify that he or she wants such treatment to stop if doctors determine that there is no hope of recovery (Cheeseman). Without a living will in place your family members and doctors have to play the guessing game when it comes to the type of treatment one wish to have if they are seriously ill and becomes unable to communicate or make those types of decisions for themselves. Although a living will lets healthcare professionals and family members know who should be informed or involved in treatment decisions (Haas), they may not benefit from new medical treatment if they are

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Answer: if someone passes away and they do not have a will, their estate will enter intestate procedures. Each state has different procedures for handling assets these assets, but the fundamentals are technically the same. Within most states a percentage of the assets (ranging from half to two thirds) will go to the deceased children, with the remaining going to the spouse. If one of the parties mentioned above are non-applicable, the assets would shift fully to the applicable party. Complication may arise is there are no children or spouse alive.

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but a Hospice practitioner may not be available for a face-to-face. The thought is that with all of the documentation and need for an encounter, it will cut down on fraudulent long term

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Oftentimes, grief can be a challenging thing to overcome as a healthcare provider. It not only stymies people from making sound decisions, but it can end up with blame focused in areas where it should not be. This is with particular regard to patient families. In the case of this 72-year-old patient, there are a number of issues in this situation that are both unethical and downright illegal, including the fact that the patient’s living will is not currently being respected. Legal/Ethical issue 1: The legality of the living will parameters Both the legal and ethical issues of this situation have the do with the legality of the living will.

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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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The living will protects a person’s predetermined choices relating to how their physician carries out their health care or end-of-life care in the event that they become unconscious or mentally incapable. Write your living

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This would include having a good family network and that funeral arrangements are in place. An end of life care plan would have to be set in place and a will would have to be made with the individual input and best interest in place if lacking capacity at the time of writing one. We need to ensure that we keep regular contact with GP’s

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It is nearly impossible for the patient to rely on another person to make the best decision that they would have made for themselves, particularly when it involves personal interests such as profiting from a will. If there is something to gain, the family members’ motives seem questionable. If the patient falls ill, then there lies a possibility that their heirs will hope for the patient’s death so that they could receive their inheritance. The inability to confirm whether the family actually has the patient’s best interest in mind supports the argument that any form of euthanasia is unethical. Moreover, health care costs for terminally ill patients, including nursing homes, prescription drugs, and home health care deserves consideration.

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It aims to provide comprehensive and compassionate care for individuals with terminal illnesses, focusing on pain management, symptom control, and emotional support for both patients and their families. To qualify for the benefit, individuals must have a life expectancy of six months or less if the illness progresses as expected and must choose to forgo curative treatment (Rubin, 2015). In the situation involving Barbara Smith, the policy applied initially when her prognosis of coronary artery disease (CAD) indicated a life expectancy of six months or less. As per the policy's requirements, Barbara was referred to hospice care.

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When a terminally ill patient undergoes long and grueling unsuccessful treatments, the patient may lose a sense of hope for living and accept their death. Then they may go on to wanting control over their death and leading a patient to pursue PAS. Terminally ill patients are usually weak, tired, and uncomfortable. These are some of the main factors that qualify a patient for PAS because they interfere and prevent the patient from having a good quality of life. In addition, a patient may request PAS to lessen the financial burden of unnecessary medical procedures.

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As people mature,they often experience stages of development which may not reflect reality. Teenagers often view the world through their preconceived ideas or through what they want events or others to be, and inaccurate represents may control thoughts and actions. The protagonists Pip in Charles Dickens’s Great Expectations and Henry in Stephen Crane’s The Red Badge of Courage struggle to separate what is from what they desire to have occur. Although both young men come from near poverty, imagine their illustrious futures, and must face shocking disappointments, they differ in how they manage their growth processes. Pip’s parents died when he was young and he ended up living with his sister and her husband Joe, a blacksmith.

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What is Hospice? What do we as people think of when we mention the word, Hospice? “Bereavement” in other words that is not always a true statement. I now been with Hospice going on three years; June 17 2016. I have taken care of most of the patients I have had since day one as yes’ there are long term patients not short term.

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Imagine getting diagnosed with a terminal illness and being told your last months would be spent in extreme pain. Every day somebody is diagnosed with a terminal illness and is given months to live and most of those months are spent in extreme pain that is controlled by multiple medications. Hospice care is available to help their pain in the end, but they usually cannot speak for themselves at that point. Physician-assisted suicide would allow them to choose when, where, and how they die, and their death would be quick and painless. Not only does this help the patient, but it also helps the family cope with the loss.

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Death is a natural process that will be experienced by everyone at some point, desirably at the end of a long, well lived life. The reality is that no one knows when that time will come or how it will happen. Unfortunately, for the terminally ill, death is in the near future and it is a sobering reality. Therefore, when that time comes, people need to know that they will have options, and the assurance that death does not have to be an agonizing end. They can choose to endure the annihilating pain that comes with the disease and allow it to take its natural course or choose to put an end to it, surrounded by those who love them.

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Hospice and palliative care can be easily intertwined; they are both concerned with promoting comfort and relieving patient pain. Hospice and palliative care, however, are different in some aspects. Patients who receive hospice care are nearing the end of their lives and there is no effort to cure their disease; the goal is to provide pain relief, a sense of belonging from family and friends if desired, support through the dying stages, and to assure that the person is able to die with dignity. Palliative care is also focused on reducing discomfort; however, the patient receiving care can be at any stage in their disease. Additionally, palliative care can also be administered during a time when a patient is receiving treatment to cure their illness.

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1566 Words | 7 Pages

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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