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...
Click to read, http://go.solvecfs.org/webmail/192652/53267832/5b9bbfcdab48d0d1ba6db90d1afacd9c5469133f4a3ad7914f41b9aa368f734e Their Facebook...
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