Campaign for Equal ME/CFS Funding at the NIH! by Bob and Courtney Miller | May 4, 2015 | HomepageA call for equal funding for chronic fatigue syndrome at the NIH
Hearing Requested for Denial of Treatment For ME/CFS by Bob and Courtney Miller | Mar 4, 2015 | Advocacy, Homepagetreatment for me/cfs, advocacy, me, cfs, SEID, congress hearing,
Madame Secretary Meet the ME/CFS Community: The $50 Million Dollar Research Funding Campaign Pt. II by Bob and Courtney Miller | May 12, 2014 | Advocacy, HomepageAsk Shirley Mathew Burwell to fulfill President Obama's promise to make ME/CFS a priority at the NIH
ME/CFS Patients Call To Action: Advocates Call for FDA to Hold ‘Real’ FDA Stakeholder’s Meeting by Bob and Courtney Miller | Jun 24, 2013 | Advocacy, FDAME/CFS Advocates call on FDA to produce FDA Stakeholders Meeting that this time produces a clear regulatory pathway for drug development.
Oh No! ME/CFS Community MIA Thus Far on Historic Opportunity: FDA Drug Development Workshop Needs Your Comments! by Bob and Courtney Miller | Apr 1, 2013 | Advocacy, FDAThe opportunity for the chronic fatigue syndrome to submit comments regarding drug effectiveness to the FDA Stakeholder Meeting is fast closing.