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    Who are currently the best ME/CFS researchers?

    Plenty of precedents over the last half century, many of which are contemporaries of ME/CFS. Politics. Political fingerprints once again, but somehow inadmissible.
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    Hypothesis ME/CFS as a sickness behaviour-like response to HSV-1 infection within the brain: A hypothesis, 2025, Campbell

    You won't see it much, but there's a theory of immune tolerance that might.
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    Brain Endothelial- and Epithelial-Specific Interferon Receptor Chain 1 Drives Virus-Induced Sickness Behavior and Cognitive Impairment, 2016, Blank +

    We cannot query the mice about their motivation. Fortunately, that limitation does not apply to humans. So I'd discard the entire sickness behavior model when humans are involved. Too much erudite/academic speculation regardless. We don't do shit because we feel crappy; it's a much more...
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    What can the science on the impact of acute infections on cognition tell us about ME/CFS?

    Sure. albeit I wouldn't subscribe to the sickness behaviour thing. It's a non-human model. But back to your initial observation, why wouldn't a chronic infection resemble what you position as an acute? Acute is merely less than 30 days, more or less. As a general rule of thumb. We could all...
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    Low sensitivity of abbreviated tilt table testing for diagnosing postural tachycardia syndrome in adults with ME/CFS, 2018, van Campen, Rowe & Visser

    I'm confused. OI is about sensations. POTS is definitional according to BP and HR - this omitting any nonsense from entities with a horse in the race. What falls beneath either banner is political. Is POTS real? Is an unmarried widower a bachelor? I don't need to parse down further. I've...
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    Who are currently the best ME/CFS researchers?

    I hope we don't forget the clutch of clinicians/researchers that helped keep our heads above water these last 40 years. Many of these have turned their attention to Long Covid.
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    A brief, comprehensive measure of post-exertional malaise, 2025, Jason and Chee

    Without fever, at least for most pwME. How do you convey that? Hangover-like? It makes me wonder about immune tolerance, which we lightly touched upon when it was the subject of the Nobel prize earlier. That's an entirely distinct rabbit hole.
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    Does Disbelief of Contested Illnesses Like ME Push Patients Toward Quacks?

    Yes. Maybe even more, though: Patients know most doctors are wrong. It's not even intuitive; it's basic experience speaking to the clinicians' ignorance.
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    A brief, comprehensive measure of post-exertional malaise, 2025, Jason and Chee

    I think it's a fair comparison for many pwME, period. I fear it only addresses the degree. Some pwME have cognitive disability 24/7. It takes on a darker and more grim hue in PEM. True, it's merely less common and more difficult.
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    A brief, comprehensive measure of post-exertional malaise, 2025, Jason and Chee

    I think most look at PEM as ME/CFS underscored. It's ME/CFS on steroids. The relation reduces to degrees. It may be more appropriate to come at it as an overarching reaction that, although it involves usual ME/CFS symptoms, transcends all the "normal" sequelae in terms of time-to-onset...
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    Understanding concussion in myalgic encephalomyelitis/chronic fatigue syndrome: Findings from the 2023 National Health Interview study 2025 Sirotiak+

    I am not sure this study tells us much of anything that isn't fairly obvious: ME/CFS patients with balance issues are at greater risk of falling than healthy controls. That some of those falls may result in concussions is no more relevant than some may not, or some may result in a bruise to...
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    POTS - definition, diagnosis and symptoms

    A few years back I was in a well regarded ME/CFS study that required a four-day stay in-hospital. Among tests that included constant blood work and a lumbar puncture and a couple MRIs, every few hours I was asked to stand for ten minutes while they checked my HR and BP. They must have checked...
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    Keystone symposium Long COVID and Other Post-Acute Infection Syndromes August 10-13 2025

    If true, medicine can probably trash about 99% of all the Lyme tests performed over the last 40 or so years.
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    Development and validation of blood-based diagnostic biomarkers for [ME/CFS] using EpiSwitch®… 2025, Hunter et al. (Oxford Biodynamics)

    I appreciate the point you are trying to make, but I'm not sure how it applies in the real world. Even though the KCNJ2 gene mutation and its relation to ATS were discovered back around 2000, and even though ATS is indeed a channelopathy, it is nevertheless still referred to as a syndrome, and...
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    Development and validation of blood-based diagnostic biomarkers for [ME/CFS] using EpiSwitch®… 2025, Hunter et al. (Oxford Biodynamics)

    Andersen-Tawil Syndrome, a channelopathy, is confirmed by testing for the KCNJ2 genetic marker. ATS has several clinical features that are fairly hard to miss, but they are missed regularly by competent physicians, and at the expense of the patient. Why? Probabilities. Clinicians are taught...
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    Guardian piece on"Lyme"

    Yes, yes, yes and yes. So, all of the above. Nod. But what I was trying to convey is not to place too much value in whatever they might think - they are far too wrong far too often at the expense of people like us.
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    Guardian piece on"Lyme"

    Me too. Many clinicians believe that a positive Lyme test from ANY lab is meaningless after an accepted treatment. Ok, but I wouldn't be so concerned about what any doctor deems credible when you've ME/CFS anyway - or Lyme potentially - because most don't bother with learning anything more...
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    Guardian piece on"Lyme"

    Again, who decides what qualifies as good practice when Gold Standards are pretty much absent in Lymeworld? It's been my experience that good vs bad practice is largely a political distinction. Diagnostics remain a coin flip, treatment success seem still dependent on timing, and even with...
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