How to Build the ME/CFS Field: The NIH Wants Your Input
The NANDS Council Working Group for ME/CFS Research is a NINDS (National Institute of Neurological Disorders and Stroke) effort designed to get NINDS off its butt (so to speak) and accelerate the research done on ME/CFS. It will ask NANDS – the group which...
Could Craniocervical Instability Be Causing ME/CFS, Fibromyalgia & POTS? Pt I – The Spinal Series
I never would have guessed this was the solution to my ME/CFS. Jeff, on Phoenix Rising Jeff had a typical ME/CFS onset: he was a young, healthy and active individual before being felled by a viral infection and a high temperature. The infection left him with...
“Now is the Time”: Massive Online and Local Events Promise to Push ME/CFS Forward
ME/CFS advocacy is growing and growing. We have two groups, ME Action (join it here) and the Solve ME/CFS Initiative working pretty much in lockstep to move forward on ME/CFS. Central to both groups’ efforts are a Senate Resolution sponsored by Senator Markey...
Unrest Flies High, Dr. Oz Talks ME/CFS and Ms Magazine Delivers
More Than Just a Film “riveting……equal parts medical mystery, science lesson, political advocacy primer and even a love story.” San Francisco Chronicle From the beginning Jen Brea’s vision has been a very large one of which Unrest was...Lives Interrupted Latest Story
Bob Graybosch
Lahaina, United States
Former occupation: Resort General Manager
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StudyME
Enroll in the OMF’s StudyME project and help bring about a cure for ME/CFS, fibromyalgia, POTS and long COVID.
