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    Does the pathology of ME/CFS include brain damage?

    Certainly. Logic. Judgement. Recall. There are others. My IQ tests would challenge that: They've dropped by almost 20 pts since I first started getting sick a quarter century ago. I frequently don't understand instructions. Each time I've traveled to the NIH to participate in a study, I've had...
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    Does the pathology of ME/CFS include brain damage?

    A bruise is damage and it isn't typically permanent. Sure, but cognitive impairment is downstream to brain damage. Besides, both brain damage and cognitive impairment are reflective of a range, a spectrum. Some of us suffer them to a greater degree than others within our own ME/CFS community -...
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    Does the pathology of ME/CFS include brain damage?

    I am unclear that there is a more accurate word than "damage". Most alternatives that I can think of (e.g. impairment, dysfunction, impediment, etc.), can connote external influences. "Damage" is specific to the victim. Moreover it spares the patient community from unfortunate and minimizing...
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    Does the pathology of ME/CFS include brain damage?

    If I had my way, SPECT scans would be SOP in ME/CFS cases. As it is, it is virtually impossible to get one anymore.
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    Does the pathology of ME/CFS include brain damage?

    But most people wouldn't be thinking of signaling or biochemical or viral persistence or immune abnormality issues. Wouldn't any of these constitute "damage"? Damage is just harm of some sort; it can be reversible or not.
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    Does the pathology of ME/CFS include brain damage?

    I would suggest that something like this or aberrant signaling would qualify as damage. It implies a change in a patient's normal brain make-up/functioning characterized by negative consequences. An additional question might be what is causing it.
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    Does the pathology of ME/CFS include brain damage?

    White matter lesions (perhaps due to hypoperfusion/hypoxia?) come to mind. And these have been known to resolve in some cases which could explain the uncommon incidences of recovery. ETA: I think things like this can boil down to can you have brain damage without apparent structural damage, and...
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    Viral infections and the risk of neurodegenerative diseases: a comprehensive meta-analysis and systematic review, 2025, Liu et al

    I wonder what the difference is between neurodegenerative diseases and neuropsychiatric ones (not including things like brain cancer.) Would ME/CFS potentially qualify as neurodegenerative? I realize there's little data in that regard, And It would have to be a very very slow progression... I...
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    Alpha-gal syndrome: Meat allergy linked to tick bites

    The generally accepted view is that climate change is behind the spread of the Lone Star tick - not to mention the AGS and and at least five other TBDs that can accompany it. There is evidence that nature may have been nudged just a little. Reportedly, in the late '60's, tens of thousands of...
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    Alpha-gal syndrome: Meat allergy linked to tick bites

    Lone Star ticks are bad-ass. They don't merely wait to clasp onto animals wandering by. They hunt. ETA: They aren't native to New Jersey.
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    How do we stop charities and influencers spreading bio-babble about ME/CFS?'

    I'm in no mood for silliness, and I'm not inclined to play games. If I recall correctly, some part of the brain's immune system has been engaged so long or so intensely that it no longer functions correctly. I cannot remember why this results in symptoms, but there are similar theories in...
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    How do we stop charities and influencers spreading bio-babble about ME/CFS?'

    Sorry, it was poorly expressed as I'm struggling. So? I think so. Maybe you should check the internet. I can appreciate how a patient's perspective may seem abstract, but trust me when I say for any of us who have been embroiled in this debacle for more than a few years, we usually can...
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    How do we stop charities and influencers spreading bio-babble about ME/CFS?'

    Generally speaking, it is my experience that although medics are well-educated, they are close-minded. They are governed by their own cultural biases just as everyone else is, but because of the arrogance that seems to be part of their ticket, and because of their direct and immediate impact on...
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    How do we stop charities and influencers spreading bio-babble about ME/CFS?'

    How do you imagine doctors get most of their information these days? ETA: In the realm of contested diseases, patients frequently know more than doctors as it pertains to their disease. The internet is in large part responsible.
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    How do we stop charities and influencers spreading bio-babble about ME/CFS?'

    Which of these is a contested disease? Which have active campaigns against them to deny they actually exist?
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    How do we stop charities and influencers spreading bio-babble about ME/CFS?'

    In many cases it is not. 1) I tend to agree that it is not neuroinflammatory but remain open to it being so. 2) It is not what has traditionally been labeled as a psychiatric disease. There are some boundaries that we should not cede, concessions we should not embrace. These are not academic...
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    How do we stop charities and influencers spreading bio-babble about ME/CFS?'

    No one associated with ME/CFS should. It could be catastrophic at the patient level. We should stick to neurological if only because of the ramifications of bowing to embedded medical biases. Protocol has its utility but it also can be counterproductive and even harmful. The patients should...
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    How do we stop charities and influencers spreading bio-babble about ME/CFS?'

    Most of us agree that there are many, many mistakes across ME/CFS, promulgated by advocates and enemies alike. Some are cringeworthy. Some are dangerous. I still would caution about tearing things down without first having something to replace them besides theory and stats and definitions and...
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    Preprint Virus Genome Sequences in the Blood of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Patients, 2025, Davis et al

    Nods. This was my thinking as well. If there is immunosuppression going on, what is making people feel sick? There seems to be a tie in to activation of latent viruses like herpes strains. But wouldn't there be evidence of those reactivations? It's a bit too convoluted for me, but there...
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    Preprint Virus Genome Sequences in the Blood of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Patients, 2025, Davis et al

    What if there is very little - next to none - replication going on? Just bleb aggregates that accrue over time in biofilms in the brain? Viral RNA released into the blood does seem like a compelling rebut, but in the absence of replication?. I am fascinated by a theory of immune tolerance...
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