Monday, July 22, 2013

weekly reflection # 7



Weekly reflection # 7
Historically, hospice care is based on a moral necessity, value of concern about human suffering and the ethical sense of responsibility to help relieve that suffering (Cowles, 2003).   The hospice care maximizes the quality of a patient’s last days and to provide his or her “safe passage”.  Family care is not substituted by hospice care but rather facilitated and supported based on the patient’s needs. 
Hospice care has a holistic perspective and a biopsychosocial perspective.  The holistic perspective gives the direct attention to the needs of the whole person which involves interaction with the spiritual person of the patient and his or her physical needs.  The biopsychosocial perspective involves biological, psychological, and social spheres of our lives interacting and affecting one another.  Fish (1994) and Germain (1984) mention that terminally ill patients often encounter a variety of physical associated discomforts, such as pain, dyspnea, weakness, eating and sleeping problems, digestion and excretion problems, sensory impairment, paralysis, skin problems, or swallowing difficulty.  My father-in-law who suffers from Parkinson’s disease and is in a bed-ridden stage has the symptoms mentioned above.  Since he is a terminally ill person, his family decided to bring him home last month.  Even though he seems more comfortable staying home rather than at hospital, he is having associated physical discomforts.  Because he weighs only 70 lbs, he is so bony and so weak.  Even though he feels pain all the time because of his muscle rigidity and pressure sores, he cannot complain about his pain because it takes a lot of his energy to speak, and as a result, he feels so sad and cries very often.  Social workers and nurses understand his pain and suffering, so they give him pain relief medication four times a day.  They look after him using holistic and biopsychosocial perspectives.
Reference
Cowles, L. A. F. (Ed.). (2003). Social work in the health field: A care perspective. (2nd ed.) Binghamton, NY: The Haworth Press.

Fish, N. M. (1994). Social work practice in hospice care. Social work practice in health care settings, 403-419.

Germain, C. B. (1984). Social work practice in health care: An ecological perspective. New York: The Free Press.

2 comments:

  1. I agree that hospice care is based on a moral necessity, value of concern about human suffering and the ethical sense of responsibility to help relieve that suffering. im really sorry about your father in law. It takes special caring people to take care of people in his condition. The social worker in hospice care service is responsible for making clients feel comfortable and painless.

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  2. Hospice does focus on a safe passage and a social worker helps to reach this status. I agree with your blog and it covered everything we discussed in chapter seven. It takes a certain and strong person to take care of patients in this profession; I know it would be hard for me to work with patients who are suffering a long with their families. Social workers are trained for these situations though and know the right ways to go about and help comfort the situation.

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