People disabled by ME and Long Covid across the UK send out an SOS. It’s time to send out our SOS signal, if we want to have funded research. May 12th, is Myalgic Encephalomyelitis Awareness Day. On this day, the #MillionsMissing of people with myalgic encephalomyelitis (ME) gather to demand an increase in research and
On May 12th, #MEAction and the #MillionsMissing are sending out an SOS to Congress to Save our Support Systems. Save our Science. Save Our Society. HERE’S WHY: Healthcare, research funding and accessibility were already incredibly fragile for people with myalgic encephalomyelitis (ME), Long Covid and the disability communities. Now, we are seeing constant threats to
#MEAction is excited to announce we are partnering with the Writers Guild Initiative (WGI) again to offer creative writing workshops for people with ME and Long COVID**. WGI has graciously donated their time to offer these writer workshops through personal mentorship with the writers of the #MEAction community! The workshops consist of three sessions during
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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