Solve’s Advocacy Paves Way for ME/CFS Research in $500M Women’s Health Funding
Solve is dedicated to opening new funding avenues for research and care for those with ME/CFS, Long Covid, and infection-associated chronic conditions and illnesses (IACCIs). Each year, we specifically advocate […]
Solve Advocacy Efforts Yield Another Victory!
Solve Advocacy Efforts Yield Another Victory! CDMRP Program at Department of Defense Announces $13.1M Grant for Long Covid Research Solve is dedicated to opening new funding avenues for ME/CFS, Long Covid, […]
The Summer 2022 Edition of The Chronicle is Available Online Now!
The electronic version of our flagship research and advocacy journal, The Chronicle, has arrived! It includes a celebration of our Long Haul Voices: Living with Long Covid and ME/CFS video […]
CDMRP Program at Department of Defense Announces $1.6M Grant for ME/CFS Research
At Solve M.E., our advocacy team is dedicated to opening new funding avenues for ME/CFS, Long Covid, and post-infection disease research and care. We’re excited to share that our efforts […]
CDMRP for ME/CFS: Navigating the Grant Application Process
Solve M.E. hosted special guest, Cecilia Dupecher, PhD Program Manager for PRMRP at the Congressionally Directed Medical Research Programs (CDMRP) for an informational webinar designed to better inform and prepare […]
CDMRP for ME/CFS: Navigating the Grant Application Process
The FY22 Defense Appropriation provides funding to support therapeutic research related to medical threats, and treatments for Service Members in current and future battlefield settings. The managing agent for the […]
President Biden Signs FY22 Budget: Wins for ME/CFS and Long Covid
Support Research, Support Patients A recent survey from our friends at Research!America found that over 80% of Americans believe our government should fund “basic scientific research that advances the frontiers […]
Honoring People with ME/CFS for Invisible Disabilities Week
As we strive to make myalgic encephalomyelitis, otherwise known as chronic fatigue syndrome, or ME/CFS, more diagnosable and treatable, we are always aware that many people suffer with this disease […]
Advocacy Success! Florida Members of Congress Take Action for ME/CFS
Florida Members of Congress Take Action for ME/CFS Solve M.E. teamed up with local Florida advocates to launch a lightning advocacy action with huge success this week. Congressmen Gus Bilirakis […]
Big News in ME/CFS Research Funding
CDMRP Funding Announcement Comes Just 24 Days After Congress Opens Potential $350 Million to ME/CFS Researchers ME/CFS researchers can compete for 5 new funding streams and over 100 awards, up […]
Victory! Six Major Federal Wins for ME/CFS
Dear Friends, Throughout 2019, I reported on our advocacy gains for ME/CFS. Thank you for standing with me and our advocacy partners during a particularly turbulent year while we fought […]
