Join Us For Solve M.E. Advocacy Week!
We are so excited to announce that next year’s Solve M.E. 2023 Advocacy Week will
December 21, 2022
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
Advocacy Month is an opportunity to share the policy solutions vital to address the growing
Support Research, Support Patients A recent survey from our friends at Research!America found that over
By Emily Taylor, Vice President of Advocacy and Community Engagement, Solve M.E. This essay was
The National Institutes of Health (NIH) recently published a long-expected request for applications (RFA) for