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Current clinical practice focuses predominantly on the patient's medical needs. However, emerging evidence suggests that psychosocial factors significantly influence decisions regarding health care choices, palliative care and attitudes about living and dying with ALS. The analysis of gaps in this area of care indicates that there is a lack of focus, and in some cases, a lack of awareness regarding the importance of addressing psychosocial concerns in patients with ALS. Many physicians feel uncomfortable in approaching patients to offer psychosocial support, and others do not know what type of psychosocial care is needed.
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Promoting Excellence in End-of-Life Care is a national program of The Robert Wood Johnson Foundation dedicated to long-term changes in health care institutions to substantially improve care for dying people and their families. Visit PromotingExcellence.org for more resources.