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  1. Simon M

    How do we stop charities and influencers spreading bio-babble about ME/CFS?'

    That's fantastic. Thanks to you and to them.
  2. Simon M

    How do we stop charities and influencers spreading bio-babble about ME/CFS?'

    Good to know ;-). I thought we also needed people studying the biological role of its protein product. It's great that a research team are focusing on a key finding from DecodeME. Do you know how the geneticists will be approaching this e.g. looking at gene expression or how its genetics varies...
  3. Simon M

    How do we stop charities and influencers spreading bio-babble about ME/CFS?'

    Sounds promising, and the lab she works in sounds ideal. I'm also intrigued she's cofounded by ME research UK and the MRC. Are these the geneticists?
  4. Simon M

    UK Action for ME Big Survey 2025 - closes 27/1/26 (UK residents only)

    Thanks to Katherine for including a few questions in the survey that Audrey Ryback proposed. These aim to replicate and better some findings on onset age, onset triggers and significance of having relatives with ME/CFS (see this post and earlier ones).
  5. Simon M

    MRC/NIHR DecodeME Showcase meeting online and in person Nov 6th

    That is extraordinarily generous of her, and not very accurate! I got the project started and had a lucky break. But it was when Audrey stepped in that things became seriously impressive.
  6. Simon M

    MRC/NIHR DecodeME Showcase meeting online and in person Nov 6th

    I'm glad you think that. I am biased, but I've been stunned by the findings. Most of it down to Audrey (unfortunately, my health is lousy , so I've been able to contribute less and less as time has gone on). I think it's probably too soon to discuss publicly, though I'm glad you've seen the...
  7. Simon M

    Should we initiate development of a new, short questionnaire to identify PEM (to aid diagnosis)?

    Indeed, but using that logic, and without making an exception of it, DecodeME is in the same category. I don't believe that's the case for the study or its cohort, because I think questionnaires can capture valuable information. I don't think these things are widely seen on the net, though...
  8. Simon M

    Should we initiate development of a new, short questionnaire to identify PEM (to aid diagnosis)?

    It's good to have so much debate about the idea of a PEM questionnaire. I just wish my health allowed my health to get involved, but I want to make one comment now (more in the next few days if I can manage it). I think it would help if we brought in data to support or challenge some of the...
  9. Simon M

    Should we initiate development of a new, short questionnaire to identify PEM (to aid diagnosis)?

    Yes, a decent de Unfortunately, the NIH group still endorsed the DPSQ as the way to assess PEM, even though it was clearly describing something for a different. S4ME made a sufficient the NIH arguing in vain that should start developing a better tool.
  10. Simon M

    Should we initiate development of a new, short questionnaire to identify PEM (to aid diagnosis)?

    Um, agree with all that. Yes, 10x higher in Cornwall than in the lowest areas. This study found that nearly half of GPs say they find ME/CFS hard to diagnose, and this questionnaire could help a lot with that. Sounds good. My health means I can't take things forward myself, though. I think...
  11. Simon M

    Should we initiate development of a new, short questionnaire to identify PEM (to aid diagnosis)?

    I should probably have posted this earlier as it's relevant to some of the comments made above. What other PEM questionnaires are there, and what questions do they use? We have the Jason and Chee 2025 paper, and it mentions several other scales. The NIH is developing one, and @Bivoxmentions...
  12. Simon M

    A brief, comprehensive measure of post-exertional malaise, 2025, Jason and Chee

    I;ve started a new thread focusing on a potential new questionnaire to identify PEM Should we initiate development of a new, short questionnaire to identify PEM (to aid diagnosis)? Thanks to everyone here who has contributed to the idea, including @Trish @Kitty @ME/CFS Science Blog @Bivox
  13. Simon M

    Should we initiate development of a new, short questionnaire to identify PEM (to aid diagnosis)?

    Relevant data so far on which other illness do or don’t have PEM We know next to nothing about the existence or extent of PEM in other illnesses, despite it often being described as unique to ME/CFS. The term was coined by medics for the 1994 CDC/Fukuda criteria because they knew of no term...
  14. Simon M

    Should we initiate development of a new, short questionnaire to identify PEM (to aid diagnosis)?

    I think it would help PwME if we had a short questionnaire that does a good job of identifying postexertional malaise (PEM), the cardinal symptom of this illness. It could be useful in two ways: 1. Doctors, especially those in primary care, could use it to help diagnose people who have ME/CFS...
  15. Simon M

    Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes, 2022, Karczewski et al

    Interesting. I haven't looked to see if any of the genes highlighted here match with DecodeME findings. I can't access the CFS page as it doesn't support mobile browsers. How many CFS cases of the reporting from UKB? There are several different UKB definitions available, I think amounting to...
  16. Simon M

    HLA and pathogens in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and other post-infection conditions, 2025, Georgopoulos et al

    Yes, and it's a nightmare to untangle. The DecodeME analysis restricted itself to people with the white European ancestry, which simplifies things – but not a lot. One reason why HLA analysis is so challenging – population stratification HLA varies enormously even in White Europeans...
  17. Simon M

    HLA and pathogens in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and other post-infection conditions, 2025, Georgopoulos et al

    My memory is terrible, but I I am not sure the Norwegian study had found HLA alleles that reached statistical significance (merely that they were promising). I wonder when the DecodeME HLA analysis will be done?
  18. Simon M

    Sex-related cardiometabolic differences in ME/CFS patients, 2025, Hofmann, Sepúlveda, Westermeier+

    I'm not sure the relatively small sample size can support such detailed conclusions. I believe there's a rule of thumb in statistical modelling that you need 10 times as many cases as parameters. I'm not sure how many "cases" we have in this experiment, given that it's looking at male versus...
  19. Simon M

    Tom Kindlon - ME/CFS Advocate

    Congratulations, @Tom Kindlon , on this award from Trinity and that standing innovation of large group of alumni, which made me tear up. If I may say so, you and Orla looked very dapper as well. This is richly deserved – you have achieved so much over the decades.
  20. Simon M

    World ME Alliance, was previously IAFME: International Alliance for ME

    Interesting. Sian Leary was doing this job, and I would have expected her to be very good.
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