Solve Brings Army of Advocates to Capitol Hill, Presses Congress to Support the Care for Long Covid Act
Advocacy Week 2023 unites Long Covid, ME/CFS communities in an effort to educate congressional representatives, marking the first in-person gathering for the event since 2019. LOS ANGELES, CA – Today […]
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 […]
Your Advocacy In Action Part 1: ME/CFS Senate Resolution Introduced
Your ME/CFS Advocacy Week actions continue to make a difference! Senator Ed Markey, a longtime champion for people with ME/CFS and people with disabilities, introduced S. Res 633, Supporting the […]
Together, We’re Sponsoring an Historic ME/CFS Legislation!
Four Years of Advocacy has paid off! We’re Proud to have Authored and Initiated the First Ever Legislation for ME/CFS Research Funding, H.R. 7057, The Understanding COVID-19 Subsets and ME/CFS Act […]
Senate Advocacy Action: $60m for ME/CFS Research
Tell Your Senator to SUPPORT INCREASED FUNDING FOR POST-VIRAL-DISEASE RESEARCH INTO ME/CFS! Thanks to your hard work during ME/CFS Advocacy Week, the U.S. Senate is currently circulating our request to include […]
42 Members of Congress Deliver for ME/CFS
Thanks to another strong turnout from the ME/CFS advocacy community, 14 Senators and 28 Congressional Representatives joined together to sign this bipartisan letter to the U.S. Department of Health and Human […]
