Regular Use of Saline May Reduce Symptoms, Boost Energy in POTS (and ME/CFS?)
Chronic fatigue syndrome (ME/CFS) and postural orthostatic tachycardia syndrome (POTS) patients have used saline for years to feel better and recover from relapses. That’s really no surprise. The documented low blood volume in both groups suggests that saline would be...
A Biomarker for Chronic Fatigue Syndrome (ME/CFS)? Immunosignature Provides Another Possibility
A Different Look at the Immune System The ultimate goal of this work is the development of a non-subjective clinical tool for diagnosing patients with ME. Lombardi et. al. Last month Health Rising looked at a potential ion channel biomarker coming out of the NCNED in...
Ron Davis’s Strategic Approach To Understanding Chronic Fatigue Syndrome (ME/CFS)
The Open Medicine Foundation released two videos of Ron Davis talking about their work over the past couple of weeks. I got a chance to talk to Davis twice since then and to flesh out a bit more what he’s doing right now. As most people probably know, the Davis...
The Fibromyalgia Doctor’s Poll: What Kinds of Doctors Are Best?
Health Rising continues its series of blogs on basic aspects of fibromyalgia with a look at which kinds of doctors help and don’t help. From general practitioners to physiatrists (pain specialists) people with FM see a wide variety of practitioners who range...
Major Breakthrough in Chronic Fatigue Syndrome (ME/CFS)? Aussies Believe Biomarker Found
Hot Story The media reports have been sizzling! Griffith University, the home of the NCNED group in Australia that produced the study, called it “groundbreaking”. IFL Science lead off with a piece called “People With Chronic Fatigue Have A Defective...StudyME
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