This would explain the malabsorption issues I had for so many years at the start of M.E. Everything was low, proteins , omega 3, iron et...
Highlights Increased intestinal epithelium PAR2 expression and gut permeability during EAE Decreased trypsin activity and intact gut permeability...
Highlights This is the first study providing longitudinal data regarding the effect of orthostatic hypotension (OH) on small vessel disease (SVD)...
[MEDIA] https://www.omf.ngo/treatment-trials/
[MEDIA]
“It was commonly assumed that the observed alterations in the mitochondrial (energy) metabolism were a consequence of T-cell exhaustion,” said...
A team led by researchers at the Institute for Systems Immunology at JMU of Würzburg has demonstrated it is now certain that the mitochondria...
From the group: *Medical disclaimer: The facilitators of the Mindbuddy groups are not medically trained, and information from this course should...
T cells have an essential role in adaptive immunity against pathogens and cancer, but failure of thymic tolerance mechanisms can instead lead to...
I would put leaky gut in the same category as adrenal insufficiency diagnosed by chiropractors and naturopaths. I would describe them as fad...
I benefitted from taking CoQ10 years ago because my blood levels were low. Might be indirectly related to M.E. and oxidative stress(which was...
Abstract The association between the stiffening of barosensitive regions of central arteries and the derangements in baroreflex functions remains...
I think that LC on the other hand might be a persistent viral infection based on brain tissue samples obtained from deceased pts.
Jarod Younger (brain 'on fire' guy) did a small study in 2014 and found that LDN helps with pain syndromes.
Unfortunately LDN made my sleep worse in the same way Elavil(amitriptyline) did 20 yrs ago. I discontinued after 2 weeks. I don't have...
[MEDIA] The U.S. #Census is considering survey changes that would reduce #disability prevalence estimates from 14% to just 8%. Such changes are...
My M.E doctor advised me 31 years ago to do nothing, and when I started feeling better again to continue doing nothing. I guess this is still...
I got it from Bateman Horn Center: [MEDIA]
"The disabling weakness and exhaustion a person with ME/CFS experiences is so profound that "fatigue" is ...probably an insult." -Jane Cuozzo
Separate names with a comma.
