Phoenix Rising tells QMUL: release the PACE trial data
Mark Berry, Acting CEO of Phoenix Rising, presents the Board of Directors’ open letter to Queen Mary University of London (QMUL) urging them to release the PACE trial data, and hopes that other non-UK organisations will join British charities in the same request...
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Maes and Morris: Diagnosis of Myalgic Encephalomyelitis: where are we now?

Discussion in 'General ME/CFS News' started by Firestormm, Mar 1, 2013.

  1. Firestormm

    Firestormm Guest

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    Cornwall England
    Not sure if this qualifies as research, so have popped it here in the News. I'm not paying for access although others might like to I suppose.
     
    SOC and Valentijn like this.
  2. barbc56

    barbc56 Senior Member

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    It's an editorial and not research. No new information.

    I have never heard of this "journal" before but will look for some information.

    Barb

    ETA LOL!! It says editorial right at the top of Firestorm's article. Facepalm!!
     
  3. Nielk

    Nielk

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  4. JT1024

    JT1024 Senior Member

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    Massachusetts
    The good news is that one of the authors has ME and he has direct contact with many top ME/CFS researchers and physicians.

    He is a former member of this forum. At this time, his focus is solely on research and writing so he no longer participates in most forums.
     
  5. Lynne B

    Lynne B Senior Member

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    sydney, australia
    Nielk, thanks for the link. I've just trawled through the entire article. I understand its general thrust, rather than the detail, but I must say I'm impressed by the work and care involved in writing this article. I don't care where I belong, either in the neuro-immune ME or CFS category, but I'm really keen to be classified by the objective criteria the authors have developed. Maybe then, research can go into finding effective treatments.
     

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