The 13th Invest in ME Research International ME Conference, one of the premiere scientific conferences for myalgic encephalomyelitis (ME) /...
" [IMG] SolveCFS Published on Dec 12, 2018 At a recent SMCI gathering in Redwood City, Dr. Jose Montoya, a clinician who has fought for people...
Contents: SMCI This Quarter: A Summary of Our Work in Research, Advocacy and Beyond Updates from Ramsay Researchers Class of 2016 SMCI’s Research...
Congress to HHS: What's replacing CFSAC? ME/CFS must be represented! On September 6, the Secretary of Health and Human Services disbanded the...
In 2010, Solve ME/CFS Initiative (SMCI) launched the SolveCFS Biobank to connect researchers with control samples and data from both patients and...
The NIH (National Institutes of Health) recently formed The ME/CFS Working Group of the NINDS (National Institute of Neurological Disorders and...
Hi all. I have the chance for an interview with Dr. Sadie Whittaker at some point, so I wondered if you had any questions that you'd like asked?...
The first half of 2018 has yielded over 100 publications specifically addressing various aspects of ME/CFS. Reports encompass familiar domains...
Contents: Page 2 - SMCI This Quarter: A Summary of Our Work Page 5 - SMCI Welcomes Two New Members to Its Board of Directors Page 6 - What’s in a...
Solve ME/CFS Initiative’s 2nd Annual Discovery Forum, held on October 14th in Washington DC, brings together leaders from across industry,...
In this episode of “Fighting for M.E. with Carol Head,” Carol talks about ongoing work in SMCI’s research program and our efforts to storm Capitol...
This recording is the full presentation of Dr. Rick Williams, Principal Investigator for Medical & Public Health Research at RTI International...
The Solve ME/CFS Initiative (SMCI) National ME/CFS Patient Registry, developed in partnership with the Genetic Alliance and Platform for Engaging...
[MEDIA]
Tell Congress To Give ME/CFS Research a Fighting Chance! Did you know that Congress oversees a $11.9 billion medical research budget independent...
For those who aren't on the email list, the Solve ME/CFS Initiative group has updated their website. Here's the announcement from their mailing...
Blog from the Jackson Lab, an interview with Zaher Nahle of Solve ME/CFS Initiative. For our next spotlight series, I took advantage of a recent...
[IMG] Go direct to the newsletter, http://go.solvecfs.org/webmail/192652/56034262/84e1d7841020482702d2f139eb54c656adcc7b303ed3a93305e4ab13b6313018...
Solve ME/CFS Initiative’s 2nd Annual Discovery Forum, held on October 14th [2017] in Washington DC, brings together leaders from across industry,...
The Solve ME/CFS Initiative (SMCI) is in the final stages of constructing a new state-of-the-art patient registry platform. Last year, we took...
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