CNN – Millions suffer from an invisible disease: My ME / CFS story
Author: Ryan Prior Every morning, I shave, brush my teeth, and swallow a dozen pills. I look in the mirror and thank God I can
Author: Ryan Prior Every morning, I shave, brush my teeth, and swallow a dozen pills. I look in the mirror and thank God I can
Author: Llewellyn King For 10 long years, I’ve been writing and broadcasting about Chronic Fatigue Syndrome, now called Myalgic Encephalomyelitis (ME). Like all chronic
Author: Anthea Rowan Twenty million people suffer from myalgic encephalomyelitis, yet there is still no test for it, nor any approved treatment. We talk to
[embedyt]https://www.youtube.com/watch?v=0oeJClgXM-s[/embedyt] Ben Howell, one of our most dedicated volunteers, recently took the time to record a video message to share with the OMF community. Ben
This excellent ME / CFS Alert video by Llewellyn King is an interview with Dr. David Systrom, a key member of our team at the newly OMF funded
by Cort Johnson The new Harvard research center will focus on a crucial part of ME / CFS – the muscles. In May the Open Medicine Foundation
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