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    Developing a blood cell-based diagnostic test for ME/CFS using peripheral blood mononuclear cells, 2023, Xu, Morten et al

    Well, sure, and isn't that the point? To assist clinical judgment? As for predictive value, I'm sorry, but reliably predicting what is going to happen isn't necessarily part of the deal., e.g. many pathogen-based diseases, particularly in acute cases, but more contentiously in late or post...
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    Long read sequencing characterises a novel structural variant, revealing underactive AKR1C1 with overactive AKR1C2 .. severe fatigue, 2023, Oakley et

    Perhaps I'm misreading this, or it can be chalked up to awkward wording, but I am unaware that anyone has irrefutably demonstrated yet that ME/CFS has a clear heritable component.
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    Developing a blood cell-based diagnostic test for ME/CFS using peripheral blood mononuclear cells, 2023, Xu, Morten et al

    Reality? The reality is our's is a contested disease, and we need a diagnostic that cannot be contested. Moreover, we're not alone in that regard. That is not required of many diagnostics. It seems to me that really should fall under disease characteristics.
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    Developing a blood cell-based diagnostic test for ME/CFS using peripheral blood mononuclear cells, 2023, Xu, Morten et al

    I wouldn't even presume to ask for so much. Just a simple gold standard positive or negative for something definitive. That's my porridge. Something that cannot be disputed or dismissed or even minimized.
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    Developing a blood cell-based diagnostic test for ME/CFS using peripheral blood mononuclear cells, 2023, Xu, Morten et al

    We do, yes. But I doubt things will be so fortunate as that. Nice to consider, though. I would, in particular family, family first and foremost, but yes, all those rat schmucks who mischaracterized and lied about us at our lives' expense. Give me an unequivocal yes/no diagnostic. I've already...
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    UK rare disease research landscape mapped for first time

    It's seldom good to be part of a minority. :(
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    Developing a blood cell-based diagnostic test for ME/CFS using peripheral blood mononuclear cells, 2023, Xu, Morten et al

    I can think of a half dozen or more diseases - off the top of my head - where I could not care less about learning more about the disease process, politically. All I would want is a reliable yes/no diagnostic, at least in the near term. It might not move science forward, but it immediately...
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    Opinion Chronic fatigue syndromes: real illnesses that people can recover from, 2023, The Oslo Chronic Fatigue Consortium

    The plural use of syndrome is weird. Seems like an anemic attempt to disappear CFS as a discreet entity. Or maybe just a silly gesture to provoke people like us? It strikes me as a peculiar brand of juvenile.
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    Opinion Chronic fatigue syndromes: real illnesses that people can recover from, 2023, The Oslo Chronic Fatigue Consortium

    Chronic Fatigue SyndromeS? By adding that extra "s" they really devalue ME/CFS, don't they?
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    Review Epstein-Barr virus-acquired immunodeficiency in myalgic encephalomyelitis-Is it present in long COVID?, 2023, Ruiz-Pablos et al

    There are other scenarios, I fear, not the least of which is the infection - whatever it may be - persists by virtue of its own voracity and immune evasion capacity.
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    Thesis Distress and coping in ME/CFS: Understanding the role of perfectionism and self-compassion, 2022, Houston

    Sometimes I feel sorry for these kids. They seem to be trying so hard. I think she used the word "self-compassion" somehow 17 times in just the title and 4 paragraphs above. That should count for something.
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    Review Posttreatment Lyme disease syndrome and myalgic encephalomyelitis/chronic fatigue syndrome: A systematic review & comparison of pathogenesis 2023 Bai

    " Due to these factors, patients who satisfy the criteria for PTLDS may have had negative experiences in the healthcare field and experienced discrepancies between symptom onset and diagnosis. This may affect data in patients who may exaggerate symptoms to obtain care " Exaggerate symptoms...
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    Review Posttreatment Lyme disease syndrome and myalgic encephalomyelitis/chronic fatigue syndrome: A systematic review & comparison of pathogenesis 2023 Bai

    This appears to have been authored by two individuals from a psychiatry department at a university in New Jersey. Writing about disease pathogenesis. Good grief.
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    UK Covid data

    To one degree or another, whether you're pro-vaccine or against, most feel swindled and lied to. Seems every other person is pissed. Science was supposed to be society's Great Arbiter, stoic and disinterested and fair, with medicine its compassionate side. Who with any long term illness...
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    Two coronaviruses isolated from central nervous system tissue of two multiple sclerosis patients

    I have a low regard for what they can infer from serum and CSF to begin with. Out of context, this can mean a few different things. I suppose it hinges - in part - on what they mean by "neutralized".
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    Two coronaviruses isolated from central nervous system tissue of two multiple sclerosis patients

    Add Covid to the growing list of pathogenic candidates behind MS. It's such a rare thing to see someone actually testing tissue, and brain tissue at that(!), for any neurological disease.
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    Professor Akiko Iwasaki and the Yale School of Medicine research on Long Covid and post infection syndromes

    And profitable. Wouldn't want to ignore the Bayh-Doyle Act. Remember when academic research had the feel of being above smear, above the mercenary? Some people feel that may have changed a little back in 1980 with Bayh-Doyle.
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    Professor Akiko Iwasaki and the Yale School of Medicine research on Long Covid and post infection syndromes

    Part of me is appreciative of the implication in "post-acute", although it's effectively muted by "syndrome". I'm curious, too, what sort of internal political dynamics might appear considering Yale's history in at least one area they'd be looking at. I hope they give Iwasaki free rein.
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