Good grief (belatedy).
That sounds exactly like me and rather unlike what is reported for ME/CFS. I refer to them as 'stroke-like' episodes where amongst other things I have transient episodic ataxia.
I would have guessed the same and I do have some slight concerns about the reliability of self-assessment in a population wary about being associated with a 'neuropsychiatric' condition
Not addressing the underlying cause of course but by reducing inflammation associated with autoimmune diseases such as rheumatoid arthritis or lupus.
It's a little bit garbled but as far as I can tell baking soda appears to reduce inflammation by inducing the cholinergic anti-inflammatory...
Another interesting one :
Sleep Deprivation Distinctly Alters Glutamate Transporter 1 Apposition and Excitatory Transmission to Orexin and MCH Neurons
http://www.jneurosci.org/content/38/10/2505
Now I'm feeling a little sleep deprived myself so I can't quite work out whether GLT1 is solely...
I've posted this in the non-ME/CFS related section but that doesn't rule out the possibility of relevance.
Firstly a mouse model that implicates the glutamate transporter GLT-1 in the mediation of exercise induced fatigue (interesting that extracellular glutamate is increased but lactate is...
Simon Wessley once referred to PACE as "a thing of beauty" and that "HMS PACE did make it successfully across the Atlantic" (the latter being an interesting phrase in itself) ...
More from Eileen Marshall and Margaret Williams :
http://www.meactionuk.org.uk/Problems_and_Solutions.htm
No way of telling if the quotes are accurate.
The problem is that the effect on the GI tract in both cases is likely to affect the microbiome and while IBS is common in ME/CFS there doesn't appear to be any distinguishing underlying pathology of the GI tract.
If they could point to X disease where a reduction in microbiome diversity...
While it's welcome to see research that appears to chime with personal experience (when subject to a stressor my brain turns to mush) unfortunately the results are open to interpretation that might support the BPS model. No criticism of the researchers - it's just the way it is.
I could...
That's pretty much my experience as well and in comparison to the NHS there really is no comparison (obviously the NHS compares unfavourably and this was based on my experience 12 plus years ago - I'm sure it hasn't improved).
One thing I have noticed is that French doctor's aren't big on...
@Hip
This paper is pretty much as I remember it :
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3784364/
As I read that - if symptoms don't resolve within the expected week to 10 days then PCS is suspected if not diagnosed de facto. Anyway, it's an interesting 'syndrome' and one of the few...
I'm not sure this is the case. PCS not resolving after any physical brain damage is assumed to have healed brings out the usual 'psychological factors' explanations but PCS can persist for many more months or years and to assume a non-physiological reason is just lazy.
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