
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.
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.
At 5:00 pm Eastern time yesterday, we found out that the Minnesota house would be voting on a bill that would remove funding to all Long COVID grants, including #MEAction’s grant, which allows us to provide direct support to people with ME and Long COVID. This is yet another SOS moment for people in our
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:
1 thought on “Urgent Action Needed: Demand NIH Fund the ME/CFS Research Roadmap!”
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!
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