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More Federal Commitment to ME/CFS & Long Covid Research
House Appropriations Committee Includes Specific ME/CFS & Long Covid Funding Callouts This week, the House
House Appropriations Committee Includes Specific ME/CFS & Long Covid Funding Callouts This week, the House
At Solve M.E., our advocacy team is dedicated to opening new funding avenues for ME/CFS,
Our team at Solve M.E. is excited to announce that Ilise Friedman recently joined us
Since 2015, the 1-2.5 million Americans with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) have been effectively
The second episode of our three-part video series, Long Haul Voices, is available to view
Today, AIM ImmunoTech, an immuno-pharma company focused on the research and development of therapeutics to
https://www.youtube.com/watch?v=W_UFlzaNU6g&list=PLbO5abv0daLXDapXhiaVgeDJaIU66DRDA&index=1 New and timely series will amplify the experiences of individuals with Long Covid and
Advocacy Month 2022 focuses on connecting people with ME/CFS, Long Covid, and other related illnesses—brings
This week, New York Times writer Peter Coy’s piece, “Pushing ‘Long Covid’ Sufferers Too Hard
Long Haul Voices: Living with Long Covid and ME/CFS Solve M.E. is excited to announce the
Support Research, Support Patients A recent survey from our friends at Research!America found that over
The need for official data from the Centers for Disease Control (CDC) is crucial to
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