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quality of life

  1. Milo
    Thread

    Proposed model of integrated care to improve health outcomes for individuals with multimorbidities (2012) Sampalli et al.

    Please discuss. This is a model of care for ME and FM program in Nova Scotia. Proposed model of integrated care to improve health outcomes for...
    Thread by: Milo, Sep 23, 2021, 4 replies, in forum: PsychoSocial ME/CFS Research
  2. Wyva
    Thread

    The Conversation: Why governments will have to consider the costs of long COVID when easing pandemic restrictions

    Author: Richard Meade Research Fellow in Economics, and in Social Sciences & Public Policy, Auckland University of Technology He also used to...
    Thread by: Wyva, Jul 27, 2021, 1 replies, in forum: Epidemics (including Covid-19)
  3. Andy
    Thread

    Impacts of online support groups on quality of life, and perceived anxiety and depression in those with ME/CFS: a survey, 2021, Morehouse et al

    ABSTRACT Background Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a debilitating condition that can negatively affect physical...
    Thread by: Andy, Jul 11, 2021, 1 replies, in forum: PsychoSocial ME/CFS Research
  4. cassava7
    Thread

    Quality of life in functional movement disorders is as altered as in organic movement disorders, Gendre et al., 2018

    Journal of Psychosomatic Research Volume 116, January 2019, Pages 10-16 Thierry Gendre, Guilhem Carle, Francine Mesratid, Cécile Hubsch, Thomas...
    Thread by: cassava7, Jul 1, 2021, 6 replies, in forum: Health News and Research unrelated to ME/CFS
  5. rvallee
    Thread

    Pain is not the major determinant of quality of life in fibromyalgia: results from a retrospective “real world” data analysis of [FM] patients, 2021

    Objective To identify correlates of quality of life (QoL) measured with the Quality of Life Scale (QOLS) in participants of a multidisciplinary...
    Thread by: rvallee, Apr 13, 2021, 5 replies, in forum: Fibromyalgia and Connective Tissue Disorders
  6. Tom Kindlon
    Thread

    Symptoms, function and quality of life in myalgic encephalomyelitis/CFS: an Australian based, cross-sectional study, 2019, Donnelly

    From: Dr. Marc-Alexander Fluks B.Sc. Thesis Kate Donnelly Source: University of Tasmania Date: December 2019, online September 2020 URL:...
    Thread by: Tom Kindlon, Nov 7, 2020, 2 replies, in forum: PsychoSocial ME/CFS Research
  7. Andy
    Thread

    The Role of Iron Metabolism in Fatigue, Depression, and Quality of Life in Multiple Sclerosis Patients, 2020, Knyszyńska et al

    Note: The term "chronic fatigue syndrome" is used often in this paper. As far as I can see the authors actually mean "chronic fatigue", which is...
    Thread by: Andy, Sep 24, 2020, 6 replies, in forum: Health News and Research unrelated to ME/CFS
  8. Sly Saint
    Thread

    Effectiveness of Psychological Interventions to Improve Quality of Life in People With Long-Term Conditions: Rapid Systematic Review of RCTs - 2018

    Effectiveness of Psychological Interventions to Improve Quality of Life in People With Long-Term Conditions: Rapid Systematic Review of Randomised...
    Thread by: Sly Saint, Jul 6, 2020, 3 replies, in forum: Health News and Research unrelated to ME/CFS
  9. Andy
    Thread

    Explaining the long-term impact of chronic Q fever and Q fever fatigue syndrome on psychosocial functioning, 2019, Hautvast et al

    'Psych researchers in "chronic illness doesn't make for happier patients" shock'! Highlights QFS and chronic Q fever patients experience long...
    Thread by: Andy, Apr 27, 2019, 7 replies, in forum: Health News and Research unrelated to ME/CFS
  10. Andy
    Thread

    Pain is associated with reduced quality of life and functional status in patients with ME/CFS, 2018, Strand et al

    Abstract Background and aims Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is challenging to live with, often accompanied by...
    Thread by: Andy, Oct 21, 2018, 3 replies, in forum: PsychoSocial ME/CFS Research
  11. Indigophoton
    Thread

    Suicidal ideation in non-depressed individuals: The effects of a chronic, misunderstood illness, Devendorf et al, 2018

    Abstract Chronic illness is a risk factor for suicide but is often explained with depression. Research has shown an increased suicide rate in...
    Thread by: Indigophoton, Jul 11, 2018, 31 replies, in forum: PsychoSocial ME/CFS Research
  12. Andy
    Thread

    The role of spousal relationships in fibromyalgia patients’ quality of life, 2018, Huang et al

    Abstract Fibromyalgia (FM) is a chronic pain syndrome that includes debilitating symptoms such as widespread pain and tenderness, fatigue, and...
    Thread by: Andy, Feb 24, 2018, 2 replies, in forum: Fibromyalgia and Connective Tissue Disorders
  13. Cheshire
    Thread

    Patients' surveys

    Severely affected ME (Myalgic Encephalomyelitis) analysis report on questionnaire 25% ME Group (UK) 2004 Link to survey ME 2008: What progress...
    Thread by: Cheshire, Nov 12, 2017, 0 replies, in forum: Science Library (Read only)
Showing results 1 to 13 of 13