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

Discussion in 'Psychosomatic research - ME/CFS and Long Covid' started by Tom Kindlon, Nov 7, 2020.

  1. Tom Kindlon

    Tom Kindlon Senior Member (Voting Rights)

    From: Dr. Marc-Alexander Fluks

    B.Sc. Thesis Kate Donnelly

    Source: University of Tasmania Date: December 2019, online September 2020 URL:
    cfsandmore, Ravn, Hutan and 10 others like this.
  2. Trish

    Trish Moderator Staff Member

    Isn't this just confirming that the ones with the worst core symptoms on one questionnaire had the worst function and QOL on another questionnaire?

    As an undergraduate study this seems fair enough - learning to collect and analyse data and discuss it. The conclusions seem sensible.
    cfsandmore, Ravn, Hutan and 10 others like this.
  3. Ravn

    Ravn Senior Member (Voting Rights)

    Aotearoa New Zealand
    Not exactly news to any of us here but if all nurses had this level of understanding of ME we'd all be a lot better of.

    Nurses have been at the center of some of my best and my worst healthcare encounters, the latter being the more common occurrence.

    I hope this thesis won't just gather dust somewhere but help improve nursing practice.
    cfsandmore, Dolphin, JemPD and 4 others like this.

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