Death of a lifestyle: the effects of social support and healthcare support on the quality of life of persons with fibromyalgia and/or chronic fatigue syndrome

Orthop Nurs. 2004 Nov-Dec;23(6):364-74. doi: 10.1097/00006416-200411000-00005.

Abstract

Purpose: The purpose of this study was to investigate how social support and healthcare support affect the quality of life of persons with fibromyalgia and chronic fatigue syndrome.

Method: A constant comparison method was used for the qualitative portion of the research and descriptive correlational methods were used for the quantitative portion.

Conclusion: This mixed design research study suggested that social support, unlike healthcare support, is related to Quality of Life (QOL). It was also evident that subjects suffering from CFS and/or FMS do not experience high levels of social support.

MeSH terms

  • Activities of Daily Living
  • Adaptation, Psychological
  • Adult
  • Attitude to Health*
  • Cost of Illness
  • Employment / psychology
  • Family / psychology
  • Fatigue Syndrome, Chronic / prevention & control
  • Fatigue Syndrome, Chronic / psychology*
  • Female
  • Fibromyalgia / prevention & control
  • Fibromyalgia / psychology*
  • Friends / psychology
  • Humans
  • Life Change Events
  • Life Style
  • Male
  • Middle Aged
  • Needs Assessment
  • North America
  • Nursing Methodology Research
  • Patient Education as Topic
  • Qualitative Research
  • Quality of Health Care / standards*
  • Quality of Life*
  • Social Support*
  • Surveys and Questionnaires