Quality of life in chronic fatigue syndrome

Robert Schweitzer, Brian Kelly, Amanda Foran, Deborah Terry and John Whiting

Social Science & Medicine, 1995, vol. 41, issue 10, 1367-1372

Abstract: Whilst the debilitating fatigue experienced in patients suffering from Chronic Fatigue Syndrome (CFS) results in a subjective marked impairment in functioning, little research has investigated the impact of this disorder on quality of life. Forty-seven subjects with a confirmed diagnosis of CFS and 30 healthy controls were compared using the Sickness Impact Profile (SIP). A subgroup of subjects were interviewed regarding the impact CFS has had on their social and family relationships, work and recreational activities. Results from both the SIP and the interview revealed that CFS subjects had significantly impaired quality of life, especially in areas of social functioning. These findings highlight the importance of addressing the social isolation and loss of role functioning experienced by CFS sufferers.

Keywords: chronic; fatigue; syndrome; well-being; myalgic; encephalomyelitis; ME (search for similar items in EconPapers)
Date: 1995
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