The Underfinanced ME/CFS Research Field Pt I: The Facts… Plus “What Can We Do? “
(Thanks to Anne for providing this eye-opening guest blog on the funding situation facing Chronic Fatigue Syndrome (ME/CFS). Anne has pledged to donate her share of any blog donations to ME/CFS research. Part II of Anne’s series on ME/CFS funding will appear...URGENT: ME/CFS Patient ‘A C T I O N’ for Patients, Family and Friends To Support Ampligen Approval at the FDA
Organizers: Robert Miller Patient/Advocate, Cort Johnson (Health Rising) , Billie Moore (Patient Advocate) and Team Contact: 511bobmiller42@gmail.com On December 20th, ME/CFS patients rose to the Challenge and Sent in 750 personal testimonies to the FDA Advisory...StudyME
Enroll in the OMF’s StudyME project and help bring about a cure for ME/CFS, fibromyalgia, POTS and long COVID.
