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    Trial Report [Abstract] - Individualised aerobic and resistance exercise training improves exercise tolerance in individuals with [LC]: [PERCEIVE], 2025, Howden+

    Sure it's possible, but I do wander whether there is that much reason as we've seen to specifically argue for that because one already has postulated an underlying disease mechanism which undoubtedly will be complex so can swing in any direction by whatever is going on.
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    How do we stop charities and influencers spreading bio-babble about ME/CFS?'

    Is it now time for a new type of ME/CFS charity based on stuff like DecodeME? How do we know, when we don't even know whether we can convice some Bob?
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    How do we stop charities and influencers spreading bio-babble about ME/CFS?'

    I would not be suprised if this is a significant factor. For Long-Covid we saw that the organisation that followed the "most aggressive in words biobabble trend" was by far the most succesful in raising funding. Whilst some charities and researchers are struggling to get pennies together they...
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    Trial Report [Abstract] - Individualised aerobic and resistance exercise training improves exercise tolerance in individuals with [LC]: [PERCEIVE], 2025, Howden+

    I don't think one even has to go as far as argue that a possibility could exist where exercise worsens the underlying pathology, whatever that may be. There's no evidence that it has any worthwhile benefits and there's simply no point in making people feel horrible if those benefits don't even...
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    Daratumumab, isatuximab (CD38 drugs)

    I don't think so. There's a strong indication that he has no idea what he's doing or saying so I wouldn't put much value into his observations whether they are negative or positive. Besides that we have no idea what condition the patients he treats have, maybe they have the spike protein...
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    Post-Exertional Symptom Exacerbation after Sub-Maximal Exercise in Individuals with [ME/CFS] and Post-Acute Sequelae of COVID-19, 2025, Berardi et al

    Since they mention physical, cognitive, or emotional stressors as confounders for PESE they seem to be aware of some greater picture, despite their focus elsewhere. If someone believes that something is anways just people with maladaptive thoughts then they probably have no reason to think that...
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    Post-Exertional Symptom Exacerbation after Sub-Maximal Exercise in Individuals with [ME/CFS] and Post-Acute Sequelae of COVID-19, 2025, Berardi et al

    Overall the authors conclusion seems to be: Exercise should be recommended as treatment for ME/CFS as long as it doesn't trigger PEM. But the PACE trial showed that even if you recruit a group of people that don't necessarily have PEM you don't get any worthwhile treatment outcomes. Wasn't it...
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    Post-Exertional Symptom Exacerbation after Sub-Maximal Exercise in Individuals with [ME/CFS] and Post-Acute Sequelae of COVID-19, 2025, Berardi et al

    Given group differences in comorbidities do the authors clarify what they consider to be comorbid conditions? PEM and PESE are typically used as synonyms. I don't think one can critisise the authors for that. I think the actual question is whether these people experience the type of PEM...
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    Daratumumab, isatuximab (CD38 drugs)

    Do we know whether participants had close contact to each other? In times of social media things can sometimes be quite connected, I think @Utsikt mentioned that at least one of the people didn't know any of the other people, but who knows.
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    Norwegian Fluge & Mella daratumumab Haukeland trial 'ResetME' now accepting international donations

    Well done @Joan Crawford ! I hope you can now enjoy the warmth of being home with whatever beverage and food you enjoy most.
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    Should we initiate development of a new, short questionnaire to identify PEM (to aid diagnosis)?

    I can see that others have suggested that a better questionnaire for diagnosis will only have extremely limited use and that seems very reasonable to me. Especially when doctors obviously don’t care about questionnaires for things they don’t even believe in. Only a different kind of education...
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    Autonomic phenotyping, brain blood flow control, and cognitive-motor-integration in Long COVID and [ME/CFS]: A pilot study, 2025, Edgell et al

    A key result also seems to be no difference in POT(s) between patients and controls if the abstract is to be believed.
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    Traumatic brain injury - similarities with and differences to ME/CFS, including PEM

    Thanks. From that I read: Designing tracers that specifically pick up the proteins associated with CTE is difficult (or at least takes a very long time) and using other tracers makes the sort of "patchy but globally spread" proteins hard to distinguish from noise whilst the resolution from PET...
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    Traumatic brain injury - similarities with and differences to ME/CFS, including PEM

    @SNT Gatchaman sorry for this delayed and somewhat vague question: As I understand Chronic traumatic encephalopathy is both a progressive disease neurological disease and also one where post-mortem autopsies deliver conclusive results. It is linked to both p-tau aggregates as well as atrophy of...
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    The science of craniocervical instability and other spinal issues and their possible connection with ME/CFS - discussion thread

    I'm also not quite sure how this would be argued as positive evidence for anaesthesia when the exact same argument that is used as negative evidence elsewhere also applies. From what I've seen what people are saying is there have been only very few operations with subsequent remissions and...
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    Do you have small fiber neuropathy (SFN)?

    Because obviously intra-observer reproducability is not all that matters. Which is what is already well document and has been already been discussed (obviously the number gets bigger when multiple sites are biopsied since this already applies to perfectly healthy controls as shown across studies).
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    Do you have small fiber neuropathy (SFN)?

    Nobody ever said anybody had to repeat a biopsy. Please read what people write. Intra-observer reproducibility is studied. Results actually seem good but obviously that's not the point.
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    Do you have small fiber neuropathy (SFN)?

    I think in 5%-10% of those HCs have a positive IEFND. IEFND is well documented to deliver positive and negative results depending on the choice of sample, sample handling and who counts the fibers and on what day of the week. I suspect you need the kind of rigorous methodlogy we hardly ever get...
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    Is there a connection between ME/CFS and Sjogren's Syndrome? Discussion and a poll about testing

    It isn't because I was never talking about the OMF. You've been talking about other societies, neurologists and rheumatologists. That was the reference (with many of their recommendations not being fulfilled in the ME/CFS study you cited.)
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    Is there a connection between ME/CFS and Sjogren's Syndrome? Discussion and a poll about testing

    These are type of results why one needs high quality SFN research in ME/CFS not this low quality research. A high quality study would have the skin biopsy analysis blinded to the participant group, since counting intraepidermal fibers involves a large amount of subjective judgment. This is all...
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