Case studies with autopsies are not unknown, but yep, autopsies need to become a priority since the brain seems to be a logical hide and seek repository of pick-your-pathogen.
Well, there are plenty of diseases where the patient is severely disabled to the point of being bedridden with often no trace of the pathogen in blood or serum or CSF. I can think of at least four from the tick-borne disease category that qualify.
Moreover there is evidence in some circles of a...
Oh FFS, it's an absurdly inadequate and minimizing and condescending metaphor - one that should never, ever be used by so-called professionals as a lead for a serious study of decline in discrete cognitive domains. This is shameful.
ETA: I know YOU'RE not saying that @MSEsperanza . :)
"Since persistent medically unexplained somatic symptoms and somatoform disorders bring about high costs for health care systems and are among the leading causes of disability (8), it is highly relevant to investigate psychological factors that characterize and influence these symptoms and...
Post-Covid. Have they demonstrated that persistently? That the virus is gone from every possible repository in a person?
If they admit Covid can exist in priviledged sites, then it leaves the entire profession exposed to similar conclusions about other pathogens. There are too many horses in...
Plus, you're from the US, as am I, not European. Personally I'd reply with something quintessentially American, like a Bugs Bunny balloon cartoon with the caption "What a maroon!", but I realize that we need to be professional and adult. I suppose.
Oh, FFS. Groundhog Day. Again.
This medicine reduced to a closed loop, never really moving forward, just thinking it does as it feels its way around its circular path....Patients want to scream at the screen and clue in the stars as to what's happening.
I'd be curious to see a focus group comprised of patients from these GP's. I'd anonymize the GP's names and locations etc, but let the patients read the transcripts. Let the patients read how the doctors had to grapple with the concept that MUS patients might have strengths. Then I'd ask the...
That it takes a focus group to trigger an epiphany of sorts in a small group of GP's that patients are people, too, is terrifying. And infuriating. And cartoonish.
But not surprising - at least not to any of their MUS patients, I'd wager.
"A conscious effort is needed to discover patients' strengths."
Is it weird that that is exactly what I feel when evaluating most of the GP's I've come across since getting sick?
Pretty good piece. Wish they had written something like "post-acute infection(?) syndrome".
Also, this I found meaningless:
"The third challenge is that no evidence-based treatment options exist at present for long COVID, resulting in the use of a symptom management approach, which mainly...
Lyme Brain Scan Study (mentions CFS)
Some Johns Hopkins neuroimaging findings. Meh.
https://www.newswise.com/articles/neuroimaging-study-reveals-functional-and-structural-brain-abnormalities-in-people-with-post-treatment-lyme-disease?ta=home
Might be something there. Too small, too limited...
I'm sorry. :( We need people to protest horrific conditions created and maintained by others. I guess maybe it can be said "within the confines of the law." Matters of sustained oppression are difficult to resolve. I hesitate to judge the actions of one of our own unless that action was...
Sorry. I try not to post as much because I have trouble anticipating how people interpret what I write.
Antebellum. I'm afraid it's a US thing. Think "Gone With The Wind". A sort of built in cultural bias that helped sustain slavery in the US decades after it was abolished in the UK and many...
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