ME/CFS Advocate Begins Hunger Strike For Ampligen Approval
Bob Miller has been to the Vice President’s office, he’s had one and one meetings with the Director of the NIH, he’s canvassed politicians on the Hill – he’s thrown everything he can into the fight to get this disorder recognition –...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...Lives Interrupted Latest Story
Megan
Randolph, United States
Former occupation: Day care worker
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