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Page 15 of 36
  1. ME/CFS Skeptic
    Post

    ..Oxidative Stress, Exercise, and Pain in Health and Disease: Potential Role of Autonomic Regulation and Epigenetic Mechanisms, 2020, Hendrix et al

    If I understand correctly the authors argue that "although the underlying mechanisms are poorly understood, there seems to be a relation between...
    Post by: ME/CFS Skeptic, Dec 1, 2020 in forum: ME/CFS research
  2. ME/CFS Skeptic
    Post

    ..Oxidative Stress, Exercise, and Pain in Health and Disease: Potential Role of Autonomic Regulation and Epigenetic Mechanisms, 2020, Hendrix et al

    Quote from the paper:
    Post by: ME/CFS Skeptic, Dec 1, 2020 in forum: ME/CFS research
  3. ME/CFS Skeptic
    Post

    Independent advisory group for the full update of the Cochrane review on exercise therapy and ME/CFS (2020), led by Hilda Bastian

    I seem to have missed this. Sounds like great news, thanks @Caroline Struthers
    Post by: ME/CFS Skeptic, Nov 28, 2020 in forum: 2021 Cochrane Exercise Therapy Review
  4. ME/CFS Skeptic
    Post

    DecodeME - UK ME/CFS DNA study underway

    Seein the same issue: [ATTACH] If you click on 'view profile' everything is fine again
    Post by: ME/CFS Skeptic, Nov 28, 2020 in forum: ME/CFS research news
  5. ME/CFS Skeptic
    Post

    ..Oxidative Stress, Exercise, and Pain in Health and Disease: Potential Role of Autonomic Regulation and Epigenetic Mechanisms, 2020, Hendrix et al

    But the journal and the article are registered on Pubmed, so people will find it if they search for topics or if they have an email notification...
    Post by: ME/CFS Skeptic, Nov 28, 2020 in forum: ME/CFS research
  6. ME/CFS Skeptic
    Post

    CBT combined with music therapy for chronic fatigue following Epstein-Barr virus infection in adolescents: a feasibility study, 2020, Wyller et al

    Just noticed that Retraction Watch has posted this on Twitter: [MEDIA]
    Post by: ME/CFS Skeptic, Nov 27, 2020 in forum: Psychosomatic research - ME/CFS and Long Covid
  7. ME/CFS Skeptic
    Post

    Bias caused by reliance on patient-reported outcome measures in non-blinded randomized trials: an in-depth look at exercise therapy for CFS, 2020,Tack

    I have posted the Author’s Original Manuscript (AOM) on Researchgate: (PDF) Bias caused by reliance on patient-reported outcome measures in...
    Post by: ME/CFS Skeptic, Nov 26, 2020 in forum: Psychosomatic research - ME/CFS and Long Covid
  8. ME/CFS Skeptic
    Post

    Bias caused by reliance on patient-reported outcome measures in non-blinded randomized trials: an in-depth look at exercise therapy for CFS, 2020,Tack

    Thanks for this helpful suggestion. I've been reading about this and it seems that I can post the Accepted Manuscript (AM) on my personal...
    Post by: ME/CFS Skeptic, Nov 26, 2020 in forum: Psychosomatic research - ME/CFS and Long Covid
  9. ME/CFS Skeptic
    Post

    Bias caused by reliance on patient-reported outcome measures in non-blinded randomized trials: an in-depth look at exercise therapy for CFS, 2020,Tack

    To be honest, most of the arguments in our paper are not new, but well known within the ME/CFS patient community. Most of those who have been...
    Post by: ME/CFS Skeptic, Nov 25, 2020 in forum: Psychosomatic research - ME/CFS and Long Covid
  10. ME/CFS Skeptic
    Post

    Bias caused by reliance on patient-reported outcome measures in non-blinded randomized trials: an in-depth look at exercise therapy for CFS, 2020,Tack

    It's not open-access. But the first 50 people who use the link I provided on Twitter should be able to access the full-version for free.
    Post by: ME/CFS Skeptic, Nov 25, 2020 in forum: Psychosomatic research - ME/CFS and Long Covid
  11. ME/CFS Skeptic
    Post

    Bias caused by reliance on patient-reported outcome measures in non-blinded randomized trials: an in-depth look at exercise therapy for CFS, 2020,Tack

    Thanks to Tom Kindlon, Simon McGrath, and Andrew Kewley for providing thoughtful comments to earlier drafts of the analysis. Also big thanks to...
    Post by: ME/CFS Skeptic, Nov 25, 2020 in forum: Psychosomatic research - ME/CFS and Long Covid
  12. ME/CFS Skeptic
    Post

    Bias caused by reliance on patient-reported outcome measures in non-blinded randomized trials: an in-depth look at exercise therapy for CFS, 2020,Tack

    Here's a Twitter summary: [MEDIA] 2) Our analysis focuses on a discrepancy between several randomized trial that report graded exercise therapy...
    Post by: ME/CFS Skeptic, Nov 25, 2020 in forum: Psychosomatic research - ME/CFS and Long Covid
  13. ME/CFS Skeptic
    Post

    Why is ME/CFS getting so little research funding?

    Thanks but our blog focuses on numbers from the US where the biomedical view has been more influential. Large agencies such as the NIH, CDC, FDA...
    Post by: ME/CFS Skeptic, Nov 24, 2020 in forum: General Advocacy Discussions
  14. ME/CFS Skeptic
    Post

    Why is ME/CFS getting so little research funding?

    Thanks @strategist Could you give some examples of this from influential or respected sources? I think the general BPS narrative has been a bit...
    Post by: ME/CFS Skeptic, Nov 24, 2020 in forum: General Advocacy Discussions
  15. ME/CFS Skeptic
    Post

    Why is ME/CFS getting so little research funding?

    Thanks. I merely wanted to argue that the view that ME/CFS can be cured with GET/CBT (and so no further research is needed) probably isn't...
    Post by: ME/CFS Skeptic, Nov 24, 2020 in forum: General Advocacy Discussions
  16. ME/CFS Skeptic
    Post

    Why is ME/CFS getting so little research funding?

    Thanks but I don't think it has ever been generally accepted that GET and CBT cure ME/CFS, despite the controversial PACE trial paper on recovery....
    Post by: ME/CFS Skeptic, Nov 24, 2020 in forum: General Advocacy Discussions
  17. ME/CFS Skeptic
    Post

    Why is ME/CFS getting so little research funding?

    That's also an explanation that comes up a lot. I realize that many ME/CFS do not receive social benefits even if they should be entitled to...
    Post by: ME/CFS Skeptic, Nov 24, 2020 in forum: General Advocacy Discussions
  18. ME/CFS Skeptic
    Post

    Why is ME/CFS getting so little research funding?

    Thanks for sharing your view. This may be one of the most important reasons but I do wonder: why has so little non-biomedical research taken...
    Post by: ME/CFS Skeptic, Nov 24, 2020 in forum: General Advocacy Discussions
  19. ME/CFS Skeptic
    Post

    Why is ME/CFS getting so little research funding?

    Thanks @Invisible Woman I do think that we should make a distinction different views on ME/CFS 1) There are those who have argued that ME/CFS...
    Post by: ME/CFS Skeptic, Nov 24, 2020 in forum: General Advocacy Discussions
  20. ME/CFS Skeptic
    Post

    Why is ME/CFS getting so little research funding?

    Yes, that's possible but the same has been said about depression, ADHD, autism and these receive much more funding (per disease burden) than ME/CFS.
    Post by: ME/CFS Skeptic, Nov 24, 2020 in forum: General Advocacy Discussions
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