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    Autism and ME/CFS

    That was my reaction too, as an autistic person and the parent of an autistic child.
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    CENSSAS: Exploring Associations Between CENtral Sensitivity Syndromes and the Autism Spectrum

    (Incidentally I first read the study title as "Inventing Associations Between Central Sensitivity Syndromes and the Autism Spectrum", which sounds about right.)
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    CENSSAS: Exploring Associations Between CENtral Sensitivity Syndromes and the Autism Spectrum

    Something that is frequently talked about by autistic people is 'sensory seeking', ie being undersensitive to stimuli (compared to other people), hence some physical repetitive behaviours or 'stimming' (repetitive movements or fiddling) to provide a consistency of sensory feedback. I've no idea...
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    Preprint A Digital Platform with Activity Tracking for Energy Management Support in Long COVID: A Randomised Controlled Trial, 2025, Hayes et al

    Couple of things from a quick skim of the PDF: That suggests their participants were on the milder end of LC, because those with more severe symptoms would have been more likely to already be on a GP or specialist care pathway and so ineligible for the study?
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    United Kingdom: Dr Suzanne O’Sullivan (BPS neurologist)

    In the rubber hand illusion, as in other illusions, the illusory sensation is almost immediately extinguished as the brain corrects its momentary error. The initial conditioning doesn't cause the participant to go on believing that the rubber hand is their own. You could just as well argue that...
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    Low-Dose Naltrexone restored TRPM3 ion channel function in Natural Killer cells from long COVID patients, 2025, Martini et al

    Higher doses have some nasty side effects, which would be problematic both in terms of wanting to avoid harming trial participants and also possibly creating confusion in the data.
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    BJGP - Could GP's understanding and management of Long Covid and ME be improved by conceptualising those conditions in terms of 'premature frailty'?

    GPs and other HCPs often seem to have enough trouble understanding the facts of what life is like for pwLC and ME, without becoming confused with yet another 'it's a bit like this except not really' condition.
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    Effect of Pain Reprocessing Therapy vs Placebo and Usual Care for Patients With Chronic Back Pain an RCT, 2021, Asher, Gordon et al

    and conversely, if you can grit your teeth and hide the fact you're in pain, that obviously means the pain isn't that bad. There's no "correct" way to give an external idea of your internal state that will stop someone else dismissing it if that's what they want to do.
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    Iron dysregulation and inflammatory stress erythropoiesis associates with long-term outcome of COVID-19, 2024, Hanson et al

    Bookmarking this answer for the next time I try and talk to my GP about why my ferritin is low but other rbc results are OK!
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    A Thought Experiment on Muscles

    There have been occasions when I've collapsed in those scenarios but it's been more due to dizziness and a sort of momentary loss of information processing from the world around me - I briefly become unsure of what I can see and hear, or which way is up. It feels like my legs stop working at...
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    World Conference on Research Integrity

    I hadn't heard of Patricia Murray before. https://www.liverpool.ac.uk/people/patricia-murray Interested to see that she began her career as a nurse. Perhaps this helped her to see medical claims in terms of their impact on patients rather than on the researchers' careers.
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    World Conference on Research Integrity

    Saw this in a Mastodon thread today about the World Conference on Research Integrity. https://mastodon.online/@tomstafford/114301415246307147
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    Caffeine against persistent fatigue in long-COVID: a randomized clinical trial, 2025, Cardoso

    Researchers missed a trick not including healthy controls. If caffeine also improves the walk distance, perceived fatigue and so on of control participants, then they've found a treatment that can support healthy people being rehabilitated from, um, healthiness.
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    Can a simple screening test distinguish between ME/CFS sufferers and patients with ME/CFS-like symptoms?, 2025, Habermann-Horstmeier (German)

    Did they check whether all the confirmed ME/CFS diagnosed patients passed this test?
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    Brain Retraining treatment for ME/CFS and Long COVID - discussion thread

    And followed up the subjects for a year, so we could see how many *actually* recovered enough to resume their old lives, and how many ran on fumes for a few months and then crashed.
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    ‘A gift and a curse’: the benefits and limitations of self-tracking Long COVID, 2025, Jayadeva & Lupton

    It's a shame things sometimes get sensationalised to make an eye-catching title. Plenty of people don't find tracking a gift or a curse, just something that helps a bit (or doesn't).
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    Long-term effects of SARS-CoV-2 infection on blood vessels and blood pressure – LOCHINVAR, 2025, Lip et al.

    Long-term effects of SARS-CoV-2 infection on blood vessels and blood pressure – LOCHINVAR Where did they get the H?
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    Identifying and renaming inaccurate, inappropriate or minimising words, phrases, etc. in ME/CFS

    I can say the first three or four syllables of 'Deteriorative' but my chances of getting anyone else to understand the whole word would be slim! What's a word meaning the same sort of thing but easier to pronounce?
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