The individual chosen for the paper is Mrs. James, Mr. James's husband (not his real name). Mr. James is a 70-year-old gentile man that had been diagnosed with pancreatic cancer at a terminal stage. Mr. James does not wish to be admitted to a hospital or a nursing home, which is why Mrs. James had agreed to look after him at their home. This condition had been discussed with the General Practitioner, the district nursing team, and the palliative care team, who agreed to Mr. James' conditions and chose to support his wife. She took on the role as Mr. James' informal caregiver voluntarily as she values the time that she has left with her husband. However, there were instances when Mr. James was feeling severely ill and his wife was uncertain as to what needs to be done to attend to her husband. She immediately contacted the GP, the district nursing team, and the palliative care team for support. In spite of the fact that Mrs. James cherished the moments that she was able to care for her husband, there were times that she felt powerless and helpless. Her husband's condition caused her emotional and psychological stress. After several days of caring for her husband, she started to question whether she made the correct decision. The team opted to advise Mrs. James to undergo a two-day intensive palliative care course at the Dorothy House as a means for her to overcome her distress. She felt that she must be able to have a strong grip and command of her emotions so as not to show any signs of insecurity, fear, and anger. Seeing his wife strong made a big difference in Mr. James passing. He died a peaceful death at his home. After Mr. James death, the palliative care team went to Mrs. James to reassure her and offer her support. The main issues of the care plan constitute of the following: pressure area care; pain; challenges in looking after home; comfort; wifes/ family's stress; promise to keep, access or the availability of palliative care team as and when needed; psychological support; and management of medication. The article that the researcher has chosen is entitled "A Desire to Be Seen - Family Caregivers’ Experiences of Their Caring Role in Palliative Home Care" by Linderholm and Friedrichsen. ...
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The purpose of this research is to investigate the following: prevention as the basis for effective home care; management and home based care for Alzheimer patients; Alzheimer caregiver and home based care; skilled home care agencies; supporting and caring for the care givers. The new methods of diagnosing Alzheimer have made it possible for early diagnosis.
The word count is: Signature: Student’s name: Elmira Mah Date: 15/5/2013 Acknowledgements I will like to acknowledge the support and encouragement given to me from a number of people throughout this dissertation process. I will first of all start by thanking God for giving me the strength and good health to sail through this dissertation process.
A Desire to Be Seen. Family Caregivers’ Experiences of Their Caring Role in Palliative Home Care: A Critical Appraisal Introduction The individual chosen for the paper is Mrs. James, Mr. James's husband (not his real name). Mr. James is a 70 year old gentile man that had been diagnosed with pancreatic cancer at a terminal stage.
This type of research is ongoing. White, et al (2004) describes that impact of unrelieved patients on nurses is quite depressive. So support mechanism is very much important. So to deal with such challenges adequate training and education, peer supports are required.
However, several environmental factors play a role in this individual’s emotional status and attitude towards life. In addition, the hospital staff involved in the provision of care are also key in ensuring that the individual has a better quality of life in his last years (Aziz et al., 2012).
Moreover, the catheter and the colostomy bag are a burden to handle, and he is further unable to move freely. Having fulfilled his family obligations, he feels that he has no reason to live and ask his family to support his decision to have his life
ng care as well as treatments for patients having limited life span or a chronic disease, which has a chance of reoccurring or has a chance to be a cause of a prolonged suffering for the patient in order to relieve sufferings (ICSI, 2013).
The case is referred to an adult aged
Projects in this reference namely Palliative Care by Department of Health are such programs. Trainings and literature providing best practices are arranged for professionals to implement their rationale.
The writer informs that palliative care is an approach that improves the quality of life both for the patient and the family facing a problem associated with a life-threatening illness. In understanding the palliative care, this paper presents a case of Mr. Martin Cavanagh, who was diagnosed with a COPD and was undergoing an end of life care management.
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