Urgent Action Needed: Demand NIH Fund the ME/CFS Research Roadmap!

Facebook
Twitter
WhatsApp
Email

1 thought on “Urgent Action Needed: Demand NIH Fund the ME/CFS Research Roadmap!”

  1. Millions of us are suffering, some for decades, and the rolls of victims of this horrible illness are increasing rapidly since the advent of COVID19. Many of us have lost our livelihoods, financial security, relationships and autonomy. Because this illness primarily affects females, lack of funding exacerbates gender inequality in numerous realms. It ensures that many physicians do not take out illness and co-morbidities seriously. Do the right thing!

Comments are closed.

Latest News

Research Roadmap Petition

We reached 7,000 signatures on our last letter. This time, our goal is 10,000. Please sign the letter today and share it with your friends and family.

Read More »
Red rectangle with the 2025 #millionsmissing logo, then the words Share this SOS Image on your socials. the meaction logo at the bottom right corner.

Share This SOS Image On Your Socials

Please help us spread the word! Share and interact with #MEAction’s social media (we are @meactnet) and share this amazing artwork (above ⬆️ ) and a message about #MillionsMissing with your own networks. Desktop: Download by right clicking on the image or clicking on the download icon in the bottom right corner of the image. Mobile:

Read More »