Impacts of online support groups on quality of life, and perceived anxiety and depression in those with ME/CFS: a survey

ABSTRACT Background Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a debilitating condition that can negatively affect physical and mental health [1,2]. People with ME/CFS report lower perceived levels of social support, which further exacerbate challenges with mental health and has been linked to a higher prevalence of depression and anxiety in this population [3]. There are many mental health benefits associated with participation in in-person support groups; however, it is unknown if these benefits translate to online support groups [5]. Purpose To examine the perceived impacts of participation in online support groups on depression, anxiety and quality of life among people with ME/CFS. Results Responses (n = 76) to an online survey indicated positive and negative experiences with participation in online support groups. Positive experiences included a sense of belonging, validation, supportive friendships and feelings of positively impacting others. Negative experiences included jealousy, decreased hope and optimism and disagreement regarding treatment strategies. Conclusion Participation in online support groups was believed to decrease perceived feelings of depression and increase the quality of life in those with ME/CFS. No significant impacts on anxiety were found. Overall, participants reported engagement in online support groups to be a positive experience.

• Publication year

  2021

• Venue

  Fatigue: Biomedicine, Health & Behavior

• Publication date

  2021-04-03

• Fields of study

  Not labeled

• Identifiers
  DOI 10.1080/21641846.2021.1950406
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar

• No claims are published for this paper.

• No concepts are published for this paper.

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