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 
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1 thought on “Watch the Stanford Research Update on T-cells”
This is exciting research! Looking forward to more updates. Proof of autoimmunity would definitely spark interest in developing tests and treatment. I don’t mean to sound petty, but I do wish someone could suggest to Dr. Davis that using the term “chronic fatigue” in place of “Chronic Fatigue Syndrome” or “ME/CFS” is misleading to those outside of the ME/CFS research, patient, and advocate community.
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