#MEAction recognizes and celebrates Pride Month! As a community that welcomes and encompasses all, this Pride Month, we asked members of our LGBTQIA+ community to share what Pride means to them and what they have learned from this movement that they bring with them to the ME movement. Here are a few responses: Kristina Osobka-Stier
#MEAction has been hard at work continuing to advocate to the Department of Health and Human Services (HHS) on behalf of people with ME and Long COVID since our last update in May. HHS has been directed by the White House to play a leading role in coordinating the response to Long COVID and associated
#MEAction is once again excited to announce our Severe ME Artists Project 2022 that will feature work from those within the severe ME community and will be in recognition of Severe ME Day on August 8th! This project will be an opportunity for those with severe ME to showcase their art work (whether it be
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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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