Thank you message for ME/CFS Advocacy Week 2026 participants highlighting community impact at state and federal levels.

Thank you to everyone who took action during #MECFSAdvocacyWeek 2026.

You helped make sure our community is heard at the state and federal levels this year. More to come.

ME/CFS Advocacy Week 2026 Day 4: Sign letters to State Medical Boards and Chief Medical Officers, share widely, optional Zoom at 3 pm ET. Text-based graphic with cream background and red and blue writing. Text: Day 4 Sign your name to letters to State Medical Boards and Chief Medical officers.* Share with your networks! Optional Zoom call at 3 om ET. *Medical providers add your name to our clinician letter!

Today for #MECFSAdvocacyWeek: add your name to letters to State Medical Boards & Chief Medical Officers.

Community sign-on: tinyurl.com/StateMedicalBoardForm

Clinicians: tinyurl.com/ClinicianSignOnForm

Share our posts: tinyurl.com/MECFSThursdaySocials

Optional Zoom at 3 pm ET.

Solve M.E.
#pwME

Call to action for ME/CFS Advocacy Week 2026 urging people to add their name to letters for State Medical Boards and Chief Medical Officers.

Today for #MECFSAdvocacyWeek: add your name to our letters to State Medical Boards and Chief Medical Officers.

Community sign-on: tinyurl.com/StateMedicalBoardForm
Clinicians: tinyurl.com/ClinicianSignOnForm
Share our posts: tinyurl.com/MECFSThursdaySocials

ME/CFS Advocacy Week 2026 Day 3 focuses on contacting legislators to support research funding and sharing posts to amplify voices in Congress. Text based graphic on cream background with blue and red accents. Full text: Two quick actions today. No Zoom call! Contact your Senators and Representatives and ask them to support ME/CFS research funding Share our posts to help grow the number of voices Congress hears

Today for #MECFSAdvocacyWeek: make your voice heard at the federal level. This is our most time sensitive action!

1. Contact your reps: solvecfs.quorum.us/campaign/157943

2. Share our posts. Ask others to join in! tinyurl.com/MECFSFederalAdvocacyDay

#MECFS #pwME #MEAwarenessHour
Solve M.E.

Graphic stating ME/CFS has no FDA-approved treatments, urging support for medical research funding through advocacy letters.

Today for #MECFSAdvocacyWeek: make your voice heard at the federal level.

Contact your reps: solvecfs.quorum.us/campaign/157943
Share our posts: tinyurl.com/MECFSFederalAdvocacyDay

#MECFS #pwME #MEAwarenessHour

Instructional graphic urging participation in ME/CFS Advocacy Week 2026 by writing a letter to support standardized medical education.

Today's action for #MECFSAdvocacyWeek: write to your state's Patient Safety Agency.

Pre-written template ready. Takes ~20 minutes.

https://canva.link/mecfsquickstartguide