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
The Year Ahead
January 23, 2025
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As we embark on the new year, we are excited to share updates about #MEAction’s advocacy projects and community programs with you! While we focus on advancing support, research, and treatments for people with ME, we’re also closely monitoring changes to public health systems under the incoming administration, and will pivot as needed to fight
