1. Guest, the 'News in Brief' for the week beginning 28th November 2022 is here.
    Dismiss Notice
  2. Welcome! To read the Core Purpose and Values of our forum, click here.
    Dismiss Notice

social support

  1. ola_cohn
    Thread

    The Impact of a Peer Social Support Network from the Perspective of Women with Fibromyalgia: A Qualitative Study, 2021, Reig-Garcia et al

    Abstract Background: Fibromyalgia is a chronic and complex disease whose management by patients requires a high level of commitment. Patient...
    Thread by: ola_cohn, Dec 14, 2021, 0 replies, in forum: 'Conditions related to ME/CFS' news and research
  2. Dolphin
    Thread

    A meta-ethnography of people with chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME) and their support needs, 2020, Pilkington et al

    https://www.sciencedirect.com/science/article/abs/pii/S0277953620305888 Some of these have been involved with annoying papers in the past Social...
    Thread by: Dolphin, Sep 21, 2020, 24 replies, in forum: Psychosomatic research - ME/CFS and Long Covid
  3. Andy
    Thread

    Fatigue-Related Cognitive-Behavioral Factors in Survivors of Childhood Cancer, 2020, Knoop et al

    Full title: Fatigue-Related Cognitive-Behavioral Factors in Survivors of Childhood Cancer: Comparison with Chronic Fatigue Syndrome and Survivors...
    Thread by: Andy, Aug 29, 2020, 3 replies, in forum: Psychosomatic research - ME/CFS and Long Covid
  4. rvallee
    Thread

    Social Services Can Threaten Families of Children with Chronic Fatigue

    Pretty good article from Vice about the reality of social services in the UK threatening sanctions against the parents of children with ME....
    Thread by: rvallee, May 2, 2019, 10 replies, in forum: General ME/CFS news
  5. Andy
    Thread

    Could disease labelling have positive effects? An experimental study exploring the effect of the CFS label on intended social support, 2018, Noble

    Abstract Objective: Chronic fatigue syndrome (CFS) patients report limited social support, which can affect symptom severity. Friends are a key...
    Thread by: Andy, Dec 8, 2018, 9 replies, in forum: Psychosomatic research - ME/CFS and Long Covid
  6. Indigophoton
    Thread

    Effects of unsupportive social interactions, stigma, and symptoms on patients with myalgic encephalomyelitis and cfs, McManimen et al, 2018

    From Leonard Jason's group, Abstract Prior research has found a heightened risk of suicide in patients with myalgic encephalomyelitis (ME) and...
    Thread by: Indigophoton, May 10, 2018, 36 replies, in forum: Psychosomatic research - ME/CFS and Long Covid
Showing results 1 to 6 of 6