research

  1. M

    MECFS Diagnosis Medical Questionnaire

    Mecfs352 is a ‘thinktank’ of tertiary students in Australia (see also @MECFS352 on Twitter) that is building a portfolio of evidence-based information on ME/CFS. We identified ME/CFS as a serious medical problem in which most patients remain undiagnosed. We are seeking feedback on a medical...
  2. Pyrrhus

    The PolyBio Research Initiative: New ME/CFS research from some of the brightest young minds!

    A brand-new research initiative from a coalition of some of the brightest young minds in ME/CFS research:
  3. Pyrrhus

    Science: Great research summaries available from ME associations!

    For anyone who loves to read through research papers, this is a reminder that there are some great resources available from different ME associations. I've listed some links below. Feel free to post more links! UK ME Association...
  4. F

    A Unifying Hypothesis of the Pathophysiology of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS),,,,,

    A Unifying Hypothesis of the Pathophysiology of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS): Recognitions from the finding of autoantibodies against ß2-adrenergic receptors Has anybody read this? I thought we tended more to low blood pressure than high (please correct me?). I...
  5. May12th

    #RUN4ME ON Sept 14, 2019 in Ontario Canada

    Please join us on Sept 14th for Action CIND’s first annual #Run4ME. The event is a chance to raise funds for Action CIND’s Myalgic Encephalomyelitis (ME) Research Fund. Come as a participant or a spectator to cheer on our runners and walkers on a 1K/5K walk/run at Woodland Trails Scout Camp, in...
  6. nyanko_the_sane

    Read Your Doctors Notes!

    https://www.nbcnews.com/health/health-news/why-it-s-important-patients-look-their-doctor-s-note-n1019111 Sometimes it is hard to tell if your doctor actually gets what you are telling them, or if they even believe you. Having received a few shocks and surprises after reading doctors notes, I...