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quality of life

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  1. SNT Gatchaman
    Thread

    Preprint Post-Vaccination Syndrome: A Descriptive Analysis of Reported Symptoms & Patient Experiences After Covid-19 Immunization, 2023, Krumholz, Iwasaki +

    Post-Vaccination Syndrome: A Descriptive Analysis of Reported Symptoms and Patient Experiences After Covid-19 Immunization Harlan M Krumholz;...
    Thread by: SNT Gatchaman, Nov 11, 2023, 11 replies, in forum: Long Covid research
  2. Wyva
    Thread

    Psychometric validation of the French Multidimensional Chronic Asthenia Scale (MCAS) in a sample of 621 pts with chronic fatigue, 2023, Banovic et al

    Psychometric validation of the French Multidimensional Chronic Asthenia Scale (MCAS) in a sample of 621 patients with chronic fatigue Abstract...
    Thread by: Wyva, Oct 11, 2023, 0 replies, in forum: Psychosomatic research - ME/CFS and Long Covid
  3. Midnattsol
    Thread

    Anticipated stigma and quality of life among people living with chronic illnesses, 2011, Earnshaw et al

    Objectives: We examined the process by which anticipated stigma relates to quality of life among people living with chronic illnesses. We...
    Thread by: Midnattsol, Jul 27, 2023, 1 replies, in forum: Other health news and research
  4. Andy
    Thread

    Poor health-related quality of life in [POTS] in comparison with a sex- and age-matched normative population, 2023, Seeley et al

    Full title: Poor health-related quality of life in postural orthostatic tachycardia syndrome in comparison with a sex- and age-matched normative...
    Thread by: Andy, Jun 21, 2023, 0 replies, in forum: 'Conditions related to ME/CFS' news and research
  5. SNT Gatchaman
    Thread

    Impact of fatigue as the primary determinant of functional limitations among patients with post-COVD-19 syndrome, 2023, Walker et al

    Impact of fatigue as the primary determinant of functional limitations among patients with post-COVID-19 syndrome: a cross-sectional observational...
    Thread by: SNT Gatchaman, Jun 8, 2023, 7 replies, in forum: Long Covid research
  6. SNT Gatchaman
    Thread

    Patient Perspectives on the Meaning and Impact of Fatigue in Hemodialysis: A Systematic Review and Thematic Analysis of Qualitative Studies, 2019

    Patient Perspectives on the Meaning and Impact of Fatigue in Hemodialysis: A Systematic Review and Thematic Analysis of Qualitative Studies...
    Thread by: SNT Gatchaman, Mar 6, 2023, 6 replies, in forum: 'Conditions related to ME/CFS' news and research
  7. Wyva
    Thread

    The chronification of post-COVID condition associated with neurocognitive symptoms, functional impairment and (...), 2022, Nehme et al

    Full title: The chronification of post-COVID condition associated with neurocognitive symptoms, functional impairment and increased healthcare...
    Thread by: Wyva, Aug 27, 2022, 11 replies, in forum: Long Covid research
  8. Kalliope
    Thread

    BMJ: Impact of ME/CFS on the quality of life of people with ME/CFS and their partners and family members.... Vyas, Muirhead et al, 2022

    Full title: Impact of myalgic encephalomyelitis/chronic fatigue syndrome /ME/CFS) on the quality of life of people with ME/CFS and their partners...
    Thread by: Kalliope, May 3, 2022, 7 replies, in forum: ME/CFS research
  9. Sly Saint
    Thread

    The Quality of Life Scale (QOLS): Reliability, Validity, and Utilization, 2003, Burkhardt and Anderson

    Abstract The Quality of Life Scale (QOLS), created originally by American psychologist John Flanagan in the 1970's, has been adapted for use in...
    Thread by: Sly Saint, Sep 28, 2021, 0 replies, in forum: Research methodology news and research
  10. 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: Psychosomatic research - ME/CFS and Long Covid
  11. 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: Long Covid news
  12. 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: Psychosomatic research - ME/CFS and Long Covid
  13. 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: Other psychosomatic news and research
  14. 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: Other psychosomatic news and research
  15. 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: Psychosomatic research - ME/CFS and Long Covid
  16. 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: Other health news and research
  17. 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: Other psychosomatic news and research
  18. 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: Other psychosomatic news and research
  19. 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: Psychosomatic research - ME/CFS and Long Covid
  20. 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: Psychosomatic research - ME/CFS and Long Covid
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