Click here to learn more about World Vaccine Congress West Coast, 27-30 Nov 2023.
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At Solve M.E., our advocacy team is dedicated to opening new government funding avenues for
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
What a way to close out 2022! We are so grateful for your generosity throughout
We are so excited to announce that next year’s Solve M.E. 2023 Advocacy Week will
Solve M.E. VP of Advocacy Emily Taylor at #MillionsMissing in Washington, D.C. Solve M.E. Vice
In April, President Biden issued a Presidential Memorandum directing the Secretary of Health and Human
House Holds Hearing on “Understanding and Addressing Long Covid” This week, the Select Subcommittee on
Each year during Advocacy Month, we host our hallmark EmPOWER M.E. roundtable, during which patient
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,
Advocacy Month 2022 focuses on connecting people with ME/CFS, Long Covid, and other related illnesses—brings
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