HealthRising: Recovery Potentially Possible: Naviaux Talks on Chronic Fatigue Syndrome (ME / CFS)
The day after my brother’s wedding I shot down to San Diego to meet Rachel Riggs and a doctor with ME / CFS. Rachel, who has turned
TRIPLE YOUR IMPACT during Triple Giving November | All Donations to OMF are TRIPLED through December 3
The day after my brother’s wedding I shot down to San Diego to meet Rachel Riggs and a doctor with ME / CFS. Rachel, who has turned
When I first became sick, I thought I had Mono, I was so sick & so tired. I finally went to the Dr. after a
Vicky Whittemore, NIH, is the Director of the Trans ME / CFS Working Group and our champion in NIH. Slides from her presentation at the IACFSME meeting in Ft. Lauderdale,
Every time I hear a story, I am moved to tears by the resilience and hope that I find in those suffering this illness. In
With your unwavering support, OMF has become the leader in ME / CFS research. OMF is excited to announce some of our accomplishments since our founding in
As Thanksgiving approaches, I’m reflecting on what I’m most thankful for. 10 years ago I was abruptly introduced to the ME / CFS community by the sudden
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