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Join the Stanford Community Symposium via Livestream
The Open Medicine Foundation will host its Second Annual Community Symposium on the Molecular Basis of ME/CFS at Stanford University on ...
NIH Creates Council to Advance ME Research
The National Institutes of Health (NIH) has formed a new council focused on how best to advance research into myalgic ...
August 2018 — Research Roundup
August was a mixed month in the world of ME research, with some truly innovative studies coming out and a ...
Announcing Launch of the #MEAction Young Researcher Fellowship
#MEAction is thrilled to announce that we are supporting the work of two research assistants working on myalgic encephalomyelitis (ME) ...
Do You Have MCAS? Fill Out this Survey.
If you have been diagnosed with mast cell activation syndrome (MCAS), please take a minute to fill out this anonymous survey. The ...
The heart of ME? Lipkin’s Collaborative Probes the Impact of Exertion
Simon McGrath is the author of the ME/CFS Research Review blog.
The hallmark symptom of ME/CFS is post-exertional malaise (PEM), a ...
The Microbiome Hypothesis: Lipkin’s Collaborative, Part 1
Author of the ME/CFS Research Review blog, Simon McGrath, has written an article about Dr W. Ian Lipkin's theory that the body’s ...
July 2018 — Research Roundup
July was a big month for scientific research in ME! Many of the most well-known researchers and clinicians had papers ...
Learning about ME at the Dysautonomia Conference
#MEAction sent two representatives, Beth Mazur and Jaime Seltzer, to attend the 2018 Dysautonomia International Conference in Nashville last month ...
Ron Davis Receives $2.5 Million Grant from NIH
Dr Ron Davis and his team at the Stanford Genome Technology Center have received a large research grant from the ...