98% AMERICANS DEFICIENT Read This and absorb it: 98% OF AMERICAN DIETS POTASSIUM-DEFICIENT | NUTRITIONFACTS.ORG Less than 2% of Americans achieve even the recommended minimum adequate int...
https://www.healthrising.org/forums/threads/potassium-deficiency-worse-than-i-was-believing.6868/
I am new here have CFS for 14 years. Just bought a Bemer Pro. Has anyone tried this type of therapy?
https://www.healthrising.org/forums/threads/bemer-therapy.3120/
Histamine H2's effect on the production of stomach acid is well known among doctors, while histamine H2's negative effect on the heart is less known. Blocking Histamine H2 with H2 receptor antag...
https://www.healthrising.org/forums/threads/histamine-h2-a-danger-to-the-heart.6871/
Proton Pump Inhibitors (PPIs) have today become one of the world's most common medications and are frequently used, among other things for chronic acid reflux (GERD). Long-term use of these drugs...
I’m not sure this is the right place to post this, but I just went to Florida to Nancy Klimas’s clinic and wanted to give you a report. I saw a different doctor, but the whole place was amazi...
https://www.healthrising.org/forums/threads/institute-for-neuro-immune-medicine.6861/
Has anyone else seen this documentary called, "What about M.E. ? Looking for comments on this documentary.
https://www.healthrising.org/forums/threads/documentary-what-about-me.6869/
If I eat foods high in amines, I get spells where my b/p jumps really high. Because of this, a couple of times this past year I've had testing for a pheo(negative). What I did find was my norepin...
https://www.healthrising.org/forums/threads/has-anyone-ever-had-their-catecholamines-tested.6866/
THE DATA ON COVID VACCINES IN CHRONIC ILLNESS PATIENTS Slides: odysee.com
Annie 1m Hi I recently started taking Rapamycin as it is now one of the drugs about to be researched by SIMMARON RESEARCH as treatment for M.E. There has been quite a lot of anecdotal evide...
https://www.healthrising.org/forums/threads/rapamycin-and-keto-diet.6865/
I’m looking for a short (no more than 20 minutes) exercise program, preferably a video, that would be safe for ME/CFS. Can anyone recommend a program, maybe Pilates, yoga, or tai chi? I walk a ...
https://www.healthrising.org/forums/threads/safe-exercise-for-me-cfs.6863/