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  1. Simon M

    A comparison of genome-wide association analyses of persistent symptoms after Lyme disease, fibromyalgia, and ME/CFS, 2025, Hirsch et al

    Looks like they do have some interesting data for Persistent Lyme disease, but the samples are too small annd the ME cases are meaningless given those selection codes. Also, it is super easy to get false positives (or very low P values near significance) due to artefacts in the Data and even...
  2. Simon M

    Deep phenotyping of post-infectious myalgic encephalomyelitis/chronic fatigue syndrome, 2024, Walitt et al

    This isn't the main finding, but this MRI on a subset of effort preference participants while doing handgrip (I think) is very interesting and received v little attention. Though based on only 8 peeps, IIRC, so not much to hang our hat on.
  3. Simon M

    Preprint Digital health app data reveals an effect of ovarian hormones on long COVID and myalgic encephalomyelitis symptoms, 2025, Male+

    It would be interesting to know what impact the menstrual cycle has on symptoms in other illnesses.
  4. Simon M

    Donating and fundraising by people with ME/CFS - discussion thread

    I fully agree with that, largely because of the excellent analysis you’ve done show that other medical charities fund a big proportion of the research that happens, and I believe that helps open the coffers of the funding organisations. The gift aid (charities reclaiming tax already paid on...
  5. Simon M

    Incidence and Prevalence of Post-COVID-19 Myalgic Encephalomyelitis: A Report from the Observational RECOVER-Adult Study, 2024, Vernon +

    and this puts an enormous question mark over the study. The highest credible prevalence rates we have for ME/CFS, from the recent Samms/Ponting study, is 0.6%. Seems hard to believe they found the same rate of NEW cases a year in the non-Covid control group Something doesn’t add up. You would...
  6. Simon M

    Preprint Autoantibody-Driven Monocyte Dysfunction in Post-COVID Syndrome with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome, 2025, Hackel+

    A single cell RNA study from Andrew Grimson, Germain? (Maureen Hansen group) highlighted monocytes as one of the cell types difference between people with me and healthy controls. I’m not sure if monocyte differences were baseline or pre-/post Max exercise. Sorry, I’m in no state to find links...
  7. Simon M

    Relationship between major depressive disorder and [ME/CFS]: a two-sample mendelian randomization study analysis, 2025, Zhu et al

    Seriously impressive digging again on here. I’m afraid I can’t help, to pass on a couple of things Chris has mentioned to me in general. First, because UK buying bank data is so accessible, it’s used in a lot of GWAS Studies, and some of these are of questionable quality. Second, Mendelian...
  8. Simon M

    United Kingdom: ME Association governance issues

    personally, I think a charity the size of the ME Association should be working through its staff primarily, with trustees providing oversight. At the moment, the trustees appear to be micromanaging the charity and making all significant decisions. I’m sure that was necessary when the...
  9. Simon M

    United Kingdom: ME Association news

    I agree with what @Trish said about transparency, and I think we should wait to hear what they have achieved before passing judgement. I live in Wales where there is next to nothing in the way of services. ADDED that might Make things a lot easier for getting something appropriate set. From...
  10. Simon M

    Donating and fundraising by people with ME/CFS - discussion thread

    This is huge, though not anything we can expect to change in the short term given prevailing medical attitudes., likewise GP surgeries (unless there is a research breakthrough). My Dad had Parkinson's, and I think I was pointed towards Parkinson's UK multiple times by different parts of the NHS...
  11. Simon M

    Donating and fundraising by people with ME/CFS - discussion thread

    I'm not sure. How many people in the UK have been given a diagnosis? (150k?) The Samms/Ponting study last year using NHS hospital episode statistics for England stats found 100k PVFS cases. PVFS is the NHS diagnostic code most closely matching ME (there is another one for Long Covid). This...
  12. Simon M

    My experience with the vivosmart4

    I’d forgotten all about that, and I am proved useful. I’ve tried another number of devices and methods, and even the very expensive WHOOP device (which I had on a free trial) wasn’t very accurate on sleep stages. Certainly, it would sometimes tell me I was sound asleep when I was simply lying...
  13. Simon M

    Should we change our name: 'ME/CFS Skeptic'?

    Insights is an excellent word to have in the title. And implies something interesting, and distinct, in the way that simply “science“ does not. On reflection, giving that your blog will usually be promoted alongside a specific blog title, and you also have the strap line, you probably could...
  14. Simon M

    Should we change our name: 'ME/CFS Skeptic'?

    Yes! Or ME/CFS Science Searchlight I kept coming up with Spotlight yesterday. Which can mean scrutiny, but it can also mean limelight, which does not work.
  15. Simon M

    Should we change our name: 'ME/CFS Skeptic'?

    I think that captures the essence of the blog. It's the sense of someone looking with fresh eyes, combined with astonishing rigour. I would also use the word clarity to describe it: the authors' clarity of thought and the clarity that leaves in the reader's mind. "Oh, that's what going on...
  16. Simon M

    Should we change our name: 'ME/CFS Skeptic'?

    I like these. Examine can be ambiguous, implying in adjudication too much, but in the sense of a medical examination of a patient, that seems exactly right. A careful inspection of what is there, followed by drawing of conclusions based on what is found. adding these, which I think are similar
  17. Simon M

    Should we change our name: 'ME/CFS Skeptic'?

    It’s very accurate But even though It’s very much my thing, it sounds very dull, which isn’t ideal for a blog title
  18. Simon M

    Should we change our name: 'ME/CFS Skeptic'?

    I Understand why you think that, and I had the same thought when trying to come up with suggestions for you. But I encourage you to reconsider. What you do is unique, of exceptional quality and I think you can confidently claim to be doing something different (without worrying too much about...
  19. Simon M

    Should we change our name: 'ME/CFS Skeptic'?

    This seems a good simple suggestion that removes the ambiguity while keeping a short and snappy title. And I’ve Struggled to come up with anything better that removes the ambiguity and is also catchy. added: “ME/CFS research under the microscope” might be more accessible, but lacks bite.
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