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  1. ME/CFS Science Blog

    2025: The 2019/24 Cochrane Larun review Exercise Therapy for CFS - including IAG, campaign, petition, comments and articles

    Thanks! I've forgotten we had access to his response. Re-reading this a couple of years later, it seems his reply was quite unhelpful. His advice to dichotomise a continuous measure and then rating the certainty of a non-zero effect seems to go against basic statistical principles. Zero is not...
  2. ME/CFS Science Blog

    2025: The 2019/24 Cochrane Larun review Exercise Therapy for CFS - including IAG, campaign, petition, comments and articles

    Yes I think the authors of the individual trials being included is a recognition for their data being used. The fact that Galsziou was senior author is more surprising. I hope he wasn't involved in the decisions about the update and its cancellation because as senior author he clearly was an...
  3. ME/CFS Science Blog

    Preprint Post-SARS-CoV-2 Onset ME/CFS Symptoms in Two Cohort Studies of COVID-19 Recovery 2024 Jamal et al

    They simply measured ME/CFS-like symptoms" Yes agree, and it should have been done in the two studies you are reporting on!
  4. ME/CFS Science Blog

    Do diagnostic criteria for ME matter to patient experience with services and interventions?, 2023, Kielland et al

    His main arguments seem to be that recruitment was biased towards ME Association members or people affiliated with it and that it did not include patients who have recovered. But even if this was only a subgroup who had bad experiences with current services, it would be cause of concern (e.g...
  5. ME/CFS Science Blog

    Mind and Body in the Guardian again

    Got the same impression when looking into psychosomatic theory for other diseases. It was usually presented as a progressive view and contrasted with genetic determinism. People like Kubler-Ross and Bettelheim believed that patients with schizophrenia/autism had no biological abnormalities...
  6. ME/CFS Science Blog

    If ME/CFS research got £1 billion, what would stop it being wasted?

    Yes but even in this area it does not look impressive. The RECOVER study on ME/CFS post-covid did not include medical examinations so it was worse than the EBV studies we have.
  7. ME/CFS Science Blog

    If ME/CFS research got £1 billion, what would stop it being wasted?

    Isn't that what happened in the US with the Long Covid money?
  8. ME/CFS Science Blog

    2025: The 2019/24 Cochrane Larun review Exercise Therapy for CFS - including IAG, campaign, petition, comments and articles

    Quote from the retraction watch article: Back in 2019, we made an overview of guidelines and policies that referred to the GET review here: https://www.s4me.info/threads/the-influence-of-the-cochrane-review-on-get.11768/
  9. ME/CFS Science Blog

    Cochrane Review: 'Exercise therapy for chronic fatigue syndrome', Larun et al. - New version October 2019 and new date December 2024

    Where did this funding come from? Was it a government grant that they lost or simply overall budget cuts?
  10. ME/CFS Science Blog

    2025: The 2019/24 Cochrane Larun review Exercise Therapy for CFS - including IAG, campaign, petition, comments and articles

    Yes GRADE recommends downgrading for imprecision if the CI crosses the threshold of interest. Which is the case here.
  11. ME/CFS Science Blog

    2025: The 2019/24 Cochrane Larun review Exercise Therapy for CFS - including IAG, campaign, petition, comments and articles

    I noticed that Lillebeth Larun has now responded to a comment: https://www.cochranelibrary.com/cdsr/doi/10.1002/14651858.CD003200.pub9/detailed-comment/en?messageId=446137675
  12. ME/CFS Science Blog

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

    Thanks for all the comments and suggestions. We have just posted the following poll on social media based on 3 options that we like the best thus far. Which name should we choose for our account and blog? 1) ME/CFS Science 2) ME/CFS In Depth 3) Science unravelled 4) None of the above (keep...
  13. ME/CFS Science Blog

    Misdiagnosis of an underlying medical condition as Conversion Disorder/Functional Neurological Disorder (CD/FND), 2020, van der Feltz-Cornelis et al

    https://eprints.whiterose.ac.uk/164981/1/20200428ConversiondisordermisdagnosisGHPaccepted_combined_1_.pdf
  14. ME/CFS Science Blog

    Deep Sequencing of BCR Heavy Chain Repertoires in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome, 2025, Ryback et al

    Thanks. The data is in .raw filetype and have some trouble converting it to something like CSV or Excel. Anyone who has more experience in this?
  15. ME/CFS Science Blog

    Deep Sequencing of BCR Heavy Chain Repertoires in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome, 2025, Ryback et al

    This study is listed on MapME/CFS but it doesn't include the raw data from what I can see, only summary statistics of their analyses and modelling.
  16. ME/CFS Science Blog

    Deep Sequencing of BCR Heavy Chain Repertoires in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome, 2025, Ryback et al

    Just posting the main results here: The Japanese used next-generation sequencing (NGS) and got the following results: They also found that it was related to an infectious-onset and shorter illness duration (perhaps that explains why Ryback only seem to find it in the mild/moderate but not...
  17. ME/CFS Science Blog

    Deep Sequencing of BCR Heavy Chain Repertoires in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome, 2025, Ryback et al

    Any ideas at what this may point to? If it is not specific antigen driven expansion, what else might be causing this? And why would B-cell abnormalities make sense, as Nath said, if it is likely not related to a specific antigen drive?
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