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

comic book background with yellow and blue colors with dots. In the center is a starburst with the words 2024 advocacy highlights. the middle is surrounded with exclamation marks.

Why You Should Gift to #MEAction this Season

December 12, 2024 No Comments

As #MEAction prepares for the year ahead, I’m thrilled to share with you a few highlights from the incredible advocacy projects our staff has undertaken this past year. As you prepare for the holidays, I humbly ask that you consider making a gift to #MEAction today to keep our work going strong! Donate We Organized

Support Keeping Telehealth – Take Action Today!

December 11, 2024 3 Comments

Expanded telehealth coverage for Medicare is set to expire at the end of this year, December 31st! Learn More #MEAction knows losing expanded telehealth will be a problem for many in our community and the wider disability community. While this action focuses on keeping the expanded Medicare coverage for telemedicine, we know that what Medicare

#MEAction Scotland volunteers in Scottish Parliament

December 6, 2024 No Comments

Volunteers from #MEAction Scotland and Long Covid Scotland talked to over 60 MSPs (Members of the Scottish Parliament) at an Information Stall in the Scottish Parliament from 5th-7th November. Ben Macpherson MSP for Edinburgh Northern and Leith sponsored the stall on behalf of #MEAction Scotland as we aimed to make MSPs aware of the desperate