Registration in now open for Solve M.E.’s 2025 Advocacy Week June 23-27!
With a new Congress and administration, we have a unique opportunity to introduce ME/CFS and associated conditions to new decision-makers and build relationships that will shape the future of research, healthcare, and support for our community. By working together, we can create champions in Washington who will help drive meaningful change.
Join us for Advocacy Week and help make sure every Member of Congress learns about these conditions and understands the urgent issues affecting millions of Americans.
This year’s Advocacy Week is 100% virtual, which means you can participate from home and make your voice heard! You’ll speak directly with policymakers (virtually) and help them understand ME/CFS and associated conditions.
No experience? No problem! Solve M.E. will schedule your meetings and provide all the training and materials you need.
Advocacy works best when people share their experiences. At the beginning of a new administration, it’s crucial to get our issues on the radar of our representatives. Investing in building these relationships now will ensure that we have champions to fight for us when we need them the most.
Visit MEForward.org to learn more about Advocacy Week 2025.
The stronger our voices, the greater our impact. Let’s make sure every leader in Washington understands the urgent need for research and care.
Registration closes on May 12. Sign up today and help us make a difference!
