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social support

  1. 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, 6 replies, in forum: PsychoSocial ME/CFS Research
  2. 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: PsychoSocial ME/CFS Research
  3. 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
  4. 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: PsychoSocial ME/CFS Research
  5. 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: PsychoSocial ME/CFS Research
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