then they later say...
I am browsing the artcile and this paragraph jumps out. To me, this is a pretty confusing and muddled statement.
Trish, did you go to the sci-hub site and then enter the doi # into their search bar? That works for me...
bump! @Jenny TipsforME, @Trish. I was able to access this paper via sci-hub.la using its doi #... https://doi.org/10.1016/j.autneu.2018.02.003...
in my case (of n=1),The vasoconstriction (which I’m assuming is there because of The cold feet Symptom) occurs intermittently at all times. this...
Jonathan, here is a description from dysautonomia international of POTS symptoms. A lot of those symptoms reflect the symptoms of many ME/CFS...
I am fine with using the term "autonomic problems” instead of dysautonomia. my observations have been that ME/CFS Patients have a range of...
I have POTS "in the technical sense". As far as, “what symptoms does it cause that are problematic?” I personally can't say. some of the symtoms...
What an potentially useful thread! I have assumed that the term “orthostatic intolerance“ was commonly used because some ME/CFS patients fall a...
@Diwi9, thanks for posting that. she is such a clear and expressive communicator. I enjoyed hearing her speculations and descriptions of her...
@Cheshire, thanks for posting that interview. seems like for a really low cost, some interesting research could be initiated. I was struck...
here is a paper co-authored by Dr. Klimas on blodd volume, etc..... "Chronic fatigue syndrome: illness severity, sedentary lifestyle, blood...
@alicec, thanks for starting this thread. your writing is clear and concise. I have been experimenting with taking amino acids and lately...
There are a couple pretty informative videos by two different autonomic dysfunction clinicians on another thread....
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