Aug 8th – Honoring the Struggle of the Severely Ill People with ME/CFS
‘An M.E. patient feels effectively the same every day as an AIDS patient feels two weeks before death.’ Mark Loveless, Infectious Disease Specialist. Today, August 8th is Severely Ill ME Day, a day created by the 25% ME Group to acknowledge, honor and...ACT NOW: Just Say NO to Funding Cuts for ME/CFS Research
Patients protest Congressional subcommittee that attempts to cut the budget for ME/CFS in half
Chronic Fatigue Syndrome Found Worse Than Diabetes, Multiple Sclerosis, Cancer, etc.
Let’s put aside questions of whether a disease is going to kill you or not and concentrate on what happens if it doesn’t kill you. Let’s say God said you had to have a chronic illness but he/she would allow you to choose which one to have. On what...
How Fibromyalgia Got to Be the Worst Funded Disease at the NIH
By some stats fibromyalgia may be the worst funded disease in the NIH. How did that happen?
The NIH’s Blindspot: The Real Reason ME/CFS and FM Funding Stinks – Conclusion
Why is the NIH funding for chronic fatigue and fibromyalgia so low. A look at the bottom forty at the NIH reveals a broad pattern of neglect.StudyME
Enroll in the OMF’s StudyME project and help bring about a cure for ME/CFS, fibromyalgia, POTS and long COVID.
