Great job @forestglip.:thumbup:
"Keeping things as simple as possible", I second that wholeheartedly.
Genetics is complicated enough even when presented as simple as possible.
:hug::hug::hug: for all the spoons you've put into this.
FND patients are educated on ingnoring symptoms,
But when the patients have done the ingnoring on their own we can always blame @dave30th ?
Neuro exams? no 1 stuck a needle in my upperleg and the leg was air-cycling on it's own. Normal? He could not help me.
No 2 was blinded by ME/CFS in the...
"struggle, unpleasant" You don't have a clue what that means in braingfog.
No it ain't broken, I think. But to call it unpleasant, to me feels like you're behaving like an elephant bull in musk inside a china cupboard.
I really so think you don't want to hurt anyone, but sometimes.....
Brainfog...
Thanks @duncan for explaining so clearly. I'm one of them too.
No major intellectual impairment, maybe, but your remark hurts @Jonathan Edwards .
Impaired most definitively. Feeling stupid; too often.
I wasn't tested as often as you were, duncan. Only once with 2-back, 3-back over a period of...
Dr. Systrom is sending frozen biopsy samples to Amsterdam (Rob Wüst), he said in an interview. They already know about capillaries.
I have diabetes and probably SFN. The neurologist I saw, left me with 3 options. Polyneuropathy or SFN or long nerve. I picked SFN.
Maybe I can find a pathologist...
Recumbent rowing? No muscle damage as seen by Wüst and co? Picking and choosing?
Cardiologists starting late in research, maybe they need some catching up first.
As a psychiatrist you've had medical training. Jack Hollis is a PsychD, does that mean he can skip everything biomedical about ME/CFS and just promote embracing symptoms and (gradual) symptom flooding as therapy without any knowledge and accountability that goes with it?
Maybe in how many years?
It would also block monoclonal antibody treatment JE wrote about.
I was once offered a DNA-test because there was a suspicion of a monoclonal T-cell population, the lab did not have enough blood tot test right away. Blood draws are often problematic. I asked my GP if the...
Why would patients need education on fatigue, they are the experts with lived experience.
Pure hybris from professionals. We don't know anything, but we can educate others with ........????????
Listening to the patients would be a good place to start.
I don't understand the anxiety gene being such a big thing. So what!!
Let all the other genes do the talking. BPS is worried, why should we. I stopped taking that crowd serious anyway.
The only thing they've ever done is claiming ME/CFS is psychological because the doctor's tests didn't show...
The frustrated ones, just acting out. Probably no knowledge about ME/CFS whatsoever. Just about the patients characters, they are all the same, females.
I was trained in iatrogenic damage by peads. It took 8 years to find meniscus and ligament were goners. Another 6 years to "find" a...
A mishap could happen? That's what Charles Shephard called it.
Patients could die from bloodletting when they already might have a lowered blood volume.
When patients don't want CBT or GET, BPS needs to convince doctors to "find" the patients for them.
A quarter of the patients "must" be MUS. (???)
What to do with them, we'll find out later. (Huh)
Is it my suspicious mind or could BPS be trying to flood the zone towards AI?
Does not matter how bad the articles are as long as they are talked about?
He can't spare a thought for the patients.
He would be so ashamed that the only right thing to do was to return the GBE.
"Sir Simon Wessely cured from his false beliefs"
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