NIH, please create a new RFA for ME/CFS

September 2, 2015

Author:

#MEAction

A group of scientists from around the country have quite recently pointed out the obvious: that ME/CFS is massively underfunded. Tell the NIH to get with the program and
1. stop refusing grants to qualified researchers
2. stop lying about refusing grants to qualified researchers
3. give ME/CFS a rightful home in the neurological disease department

Categories: Actions, Petitions, United States

Latest News

#MEAction Georgia: Voice of the Patient in Coordination with CDC & Emory School on Nursing

January 8, 2025 No Comments

Back in September, #MEAction Georgia State Chapter partnered with the Centers for Disease Control and Prevention (CDC) and Emory School of Nursing to host, Voice of the Patient: A Panel Discussion with #MEAction Georgia. This event was a continuation of #MEAction Georgia’s #MillionsMissing 2024: #TeachMETreatME programming. Erin Lee and Liz Burlingame of the #MEAction Georgia

Home Test To Treat – Findings Summary

January 7, 2025 No Comments

#MEAction and Body Politic collaborated last spring, with a new national telehealth program, Home Test to Treat. We are now able to share initial findings from the program! Here are some highlights: 80K + enrolled in the program across the country! 40K + test distributed 6K + individuals treated for COVID-19 or flu 5.6K+ organizations

Exploring the Galaxies: Day In the Life of Our Community Engagement & Social Media Manager

December 18, 2024 No Comments

Our End of Year Fundraiser: Our Community Is Out of This World is going strong! We have crossed over the 50% threshold and are working our way towards $200,000! As we shared yesterday, we have been busy fighting for you in 2024 and we do not plan on stopping in the New Year! To ensure