mcgrath

  1. MSEsperanza

    The biological challenge of myalgic encephalomyelitis/chronic fatigue syndrome: a solvable problem (2016), Edwards, JC et al

    Edwards JC, McGrath S, Baldwin A, Livingstone M, Kewley A. The biological challenge of myalgic encephalomyelitis/chronic fatigue syndrome: a solvable problem. Fatigue. 2016;4(2):63-69. doi:10.1080/21641846.2016.1160598 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867862/ Abstract Myalgic...
    • MSEsperanza
    • Thread
    • 2016 biomedical research etiology hypothesis jonathan edwards mcgrath me/cfs paper
    • Replies: 30
    • Forum: ME/CFS research
  2. Simon M

    Understanding long covid: a shortcut to solving ME/CFS? Simon McGrath

    New blog Understanding long covid: a shortcut to solving ME/CFS? Simon McGrath Understanding long covid: a shortcut to solving ME/CFS? September 17, 2020 Simon McGrath Comments 0 Comment Large numbers of people, around one in 10, don’t make a normal recovery from coronavirus but continue...
  3. John Mac

    Genetic Risk Factors of ME/CFS: A Critical Review. Joshua J Dibble, Simon J McGrath, Chris P Ponting. 2020

    https://academic.oup.com/hmg/article/doi/10.1093/hmg/ddaa169/5879704
    • John Mac
    • Thread
    • 2020 dibble genetics gwas mcgrath me/cfs paper ponting review
    • Replies: 11
    • Forum: ME/CFS research
  4. T

    PACE trial claims of recovery are not justified by the data: a rejoinder to Sharpe, Chalder, Johnson, Goldsmith and White (2017), 2017, Wilshire et al

    https://www.tandfonline.com/doi/abs/10.1080/21641846.2017.1299358 Free full text: https://www.researchgate.net/publication/315482747_PACE_trial_claims_of_recovery_are_not_justified_by_the_data_A_Rejoinder_to_Sharpe_Chalder_Johnson_Goldsmith_and_White_2017
  5. Simon M

    Leonard Jason research finds that many young people have ME/CFS (Simon M blog)

    Leonard Jason research finds that many young people have ME/CFS A new study finds that 0.75%, or 1 in 130 young people, have ME.CFS. That's a lot of people living with the illness. Only 5% of those diagnosed with the illness already had a diagnosis. Prevalence increased rapidly as children...
  6. Simon M

    There’s a yawning gap in ME/CFS research funding. Take action. (Simon McGrath blog, May 8)

    One for ME Awareness week There’s a yawning gap in ME/CFS research funding. Take action. When I got ME more than 20 years ago, I thought that science would soon provide the answers to my illness. Instead, I saw little good research going on, and there’s been a spectacular lack of progress...
  7. Sasha

    Simon McGrath launches ME/CFS Research Review science blog

    Glad to see our @Simon M launching his new blog! :thumbup: If I want to know what to make of the latest big science claim in ME/CFS research, I always look to Simon and, incredibly for a non-bioscientist such as myself, can understand what he says because he writes so clearly. I also like that...
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