
Just released! FY23 Peer Reviewed Medical Research Program (PRMRP) Funding Opportunities for ME/CFS
At Solve M.E., our advocacy team is dedicated to opening new government funding avenues for
At Solve M.E., our advocacy team is dedicated to opening new government funding avenues for
We’re joining our peer organizations at the World ME Alliance again for World ME Day
Solve M.E. and The Biotechnology Innovation Organization (BIO) will co-host a three-hour virtual event “Long
We joined 20 other members of the World ME Alliance in writing to the World
Dear advocates, allies, and friends: I’d like to take one last look back at 2022
“Mild Covid-19 disease does not lead to serious or chronic long term morbidity in the
What a way to close out 2022! We are so grateful for your generosity throughout
It’s hard to believe that we’re well into the third year of the COVID-19 pandemic,
Are you or a loved one bedbound or homebound as a result of severe or
We are so excited to announce that next year’s Solve M.E. 2023 Advocacy Week will
We’re thrilled to announce that the Chan Zuckerberg Initiative (CZI) has awarded Solve M.E. a
This week, the Milken Institute hosted their annual Future of Health Summit. Solve CEO &
350 N Glendale Ave.
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SolveCFS@SolveCFS.org
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