Urgency: Ron Davis and His (Non-NIH Funded) ME/CFS Collaborative Research Center
This is one of a series of blogs that will look at what’s coming up in 2018 from ME/CFS research foundations. Urgency Those ten NIH research center proposals contained a hidden gift. Of the ten grant applications, seven failed, leaving at least 21 potential...
Twenty-Six Years of Hell: An ME/CFS/FM Recovery Story
Patient “X” was living high when he got ill. A course creator and director for an enterprise delivering transformational experiences, X thrived on his 100-hour work weeks. From the U.S. to lndia to Australia to Germany, he made his living making a difference with...
Simmaron Patient Day Part II: Maureen Hanson, Energy and Your Immune Cells
Maureen Hanson of Cornell just scored one of the three NIH funded ME/CFS research centers in the U.S. Before she got that, though, Hanson picked up an NIH grant that enabled her to dig deeper into the energy issues of ME/CFS patients immune cells than anyone has...
Small Nerves – Big, Big Problem? Drug Trial Points Finger at Autoimmunity in Fibromyalgia and ME/CFS
Difference-Maker Unlike FMS, SFPN has identifiable pathology, physiology, and causes, and thus is definitionally a disease. Oaklander et. Al. Dr. Anne Oaklander MD, PhD, is making a difference – maybe a very big difference in the lives of many. Making a...
Chronic Fatigue Syndrome (ME/CFS) Researcher and Patients Shine During NIH Call
It’s great the NIH is doing telebriefings a couple of times a year to inform the chronic fatigue syndrome (ME/CFS) community of their progress. The calls can be more or less interesting. This one was definitely on the more interesting side. NIH Intramural Study...StudyME
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