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Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS): Major Impact on Lives of Both Patients and Family Members, Brittain et al, 2021

Discussion in 'Psychosomatic research - ME/CFS and Long Covid' started by John Mac, Jan 7, 2021.

  1. John Mac

    John Mac Senior Member (Voting Rights)

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    https://www.mdpi.com/1010-660X/57/1/43/htm
     
    Last edited: Jan 7, 2021
  2. ME/CFS Skeptic

    ME/CFS Skeptic Senior Member (Voting Rights)

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    Belgium
    Quote from the paper:
    Here's a link to the Family Reported Outcome Measure (FROM‐16): https://www.cardiff.ac.uk/__data/as...d-Outcome-Measure-FROM-16-English-version.pdf
     
    Dolphin, DokaGirl, alktipping and 8 others like this.
  3. EducateME

    EducateME Established Member

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    Merged thread

    https://www.mdpi.com/1010-660X/57/1/43

    Lovely little study and a small scale model that helped us prepare for the international research on ME/CFS impact on family members QoL.

    I know there is much more to be done, having spent half of this week in bed I have to think - baby steps, slow and steady wins the race.
     
    Last edited by a moderator: Jan 7, 2021
  4. Peter Trewhitt

    Peter Trewhitt Senior Member (Voting Rights)

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    Simon M, DokaGirl, alktipping and 3 others like this.

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