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 Goals of International Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) Awareness Day Thanks to the combined efforts of Solve M.E. and the Massachusetts ME/CFS & FM Association, […]

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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 Earlier this week, longtime ME/CFS champion Representative Jaime Raskin of Maryland’s 8th Congressional district introduced landmark legislation for ME/CFS research. This landmark legislation authorizes $60 million […]

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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 ME/CFS research funding in the next COVID-19 package. Our champion, Senator Ed Markey, is leading our initiative to include ME/CFS research funding in future COVID-19 […]

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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 Services (HHS) in support of people with ME/CFS. The bicameral letter was sponsored by Senator Ed Markey (MA) in the Senate and Congresswoman Anna Eshoo […]

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