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    Patients with severe ME/CFS need hope and expert multidisciplinary care, 2025, Miller et al

    Still too many of those horses answering: "Not my cup of tea". Confirming prejudice happens fast, changing minds takes much longer.
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    Post-COVID-Syndrome Patients Might Overestimate Own Cognitive Impairment, 2025, Wöhrstein et al.

    So do I. A few years back I did a memory test 2 -back, 3-back. Not once on location, but 3 weeks long at home. On bad moments reaction time went up 50%, misstakes doubled. That's how ME/CFS patients should be tested. Only once is a lottery.
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    Patients with severe ME/CFS need hope and expert multidisciplinary care, 2025, Miller et al

    I wonder if the witers of this piece, names not important and staff and readers of BMJ know how to use YouTube. They might want to see "Doctors with ME", by Anil van der Zee. An ass. psychiatrist and a psychiatrist pointing out that CBT is not to be used for psysical illness. And at the end of...
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    Patients with severe ME/CFS need hope and expert multidisciplinary care, 2025, Miller et al

    @dave30th called Paul Garner the O'Sullivan "poster-patient". I call him the "imposter-patient".
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    Preprint Dissecting the genetic complexity of myalgic encephalomyelitis/chronic fatigue syndrome via deep learning-powered genome analysis, 2025, Zhang+

    NASA research seems to conclude that astronauts have recurrring virus activation after 10-14 days after they arrive at ISS? Not even a microbe needed? They travel airtight and arrive airtight. No new microbe that can cause their own latent virus to come up again? A very delayed PEM? Exercise...
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    Australia: National Health and Medical Research Council (NHMRC): Development of ME/CFS guidelines

    Don't Australian doctors have to take an oath not to harm patients? When GET can cause tremendous harm, why is there still a discussion about it?
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    Collection of evidence for the efficacy of CBT/GET

    The new documentary "Doctors with ME" by Anil van der Zee, might be helpful too. Marc Vink, GP, who also published about GET, becoming very severe because of GET. You can find it at the end of the documentary. And a psychiatrist an ass. psychiatrist explaining why CBT is not supposed to be...
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    Cognitive impairment and associated neurobehavioral dysfunction in post-COVID syndrome, 2025, Schmidt et al

    Maybe they caught cognitive PEM on fMRI camera without knowing?
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    Familial coaggregation and shared familiality of functional and internalizing disorders in the Lifelines cohort, 2025, Bos et al

    Unreasonably high? I would go even further than that. I live in the Lifelines area. GP's and specialists don't "do" ME/CFS, not even the specialist chronic fatigue. The physical exam I got there was specialist and assistant taking one side each. Heart lungs and lymph. Rush job. It took me longer...
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    "Doctors as Patients" documentary Anil van der Zee

    @Grigor after having watched the whole documentary; it's way better than Hollywood productions. It's real. I'm grateful for all of you. Your documentary should become obligatory to watch for everyone working in healthcare. I meet doctors that did not have ME. They still psychologize ME/CFS...
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    "Doctors as Patients" documentary Anil van der Zee

    Thanks ever so much for this excellent documentary, @Grigor, and thanks to all that worked with you. And how sad that even medically trained people don't recognise an ME/CFS patient when one is looking straight back at them in their own mirror. Go conquer the world! Educate all ...
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    Brain Retraining treatment for ME/CFS and Long COVID - discussion thread

    The problem starts with the medics just ruling out a few bad thing, but not testing anything related to ME/CFS, concluding nothing wrong, concluding it must be psychological. Psychologists concluding now the patients are ours. That's 3 times concluding without evidence and messing up our lives...
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    Can small fiber neuropathy present like ME/CFS?

    The problem I'm left with is an unclear diagnose. Clinical picture of, but no confirmation by EMG. I was offered Gabapentin and when I turned that down, the neurologist looked at me as if had refused the lottery price. ME was in the referral letter(against my explicit wish) I mentioned brainfog...
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    Itaconate modulates immune responses via inhibition of peroxiredoxin 5, 2025, Tomas Paulenda et al

    Thank you for your dedicated, hard work and participation in the discussion on s4me!! A fool can ask more than 10 wise people can answer. I don't mind being that fool. Due to 34 years of ME/CFS out of 68, I have no reputation to protect. I was never tested on itaconate, but I had a 24-hour...
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    Can small fiber neuropathy present like ME/CFS?

    Thank you for your answer. When I'm really heated up before an EMG, does that mean in my simple words, that the nerves are wide open, to let the current run through easier? That must be vasodilation, right? I suspect vasoconstriction, OI, probably low bood volume, are causing SFN, made worse by...
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    Can small fiber neuropathy present like ME/CFS?

    I think a survey might be a good idea. Because SFN is not at all understood, bad things can happen. Last week I had an EMG for possible polyneuropathy, although I asked my GP and the neurologist to test for SFN. I didn't have enough knowlegde to object to an EMG. I was glad to get a test...
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    How does cognitive behaviour therapy reduce fatigue in patients with chronic fatigue syndrome? The role of physical activity, 2010, Wiborg, Knoop +

    Maybe this ship didn't even leave port. The captain and his senior crew were just making waves themselves, by feasting, lots of booze, that made them feel seasick. The fist that went overboard were the clients, they were not needed anymore. Just bossing them around had made the hotshots feel...
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