Tools to Help Children with ME/CFS Succeed
New resources are available to help parents and educators provide accommodations and resources to help children succeed in school.
New resources are available to help parents and educators provide accommodations and resources to help children succeed in school.
On September 8th, Nevada’s full Congressional Delegation sent a letter to Director Collins of the National Institutes of Health urging him to “strengthen and accelerate” its work on ME/CFS.
On Sept. 7, the ME/CFS community breathed a sigh of relief as the Senate Appropriations Committee recommended restoring the $5.4 million Chronic Fatigue Syndrome program under the CDC.
A national, televised program on ME/CFS aired this month on the show, “The White House Chronicle,” with host Llewellyn King.
You can now read about the details in two published pieces.
New tour dates announced: September 16 in Minneapolis and November 4 in Boston. Join us!
August 12 was an amazing day at OMF’s Community Symposium on the Molecular Basis of ME/CFS at Stanford University.
Severe ME patients publish paper questioning central findings of Dutch CBT/GET trial
The Solve ME/CFS Initiative is disappointed to report that the projected estimates for FY 17 are being reported at lower numbers than expected.
EDITOR’S NOTE: This reporting is written by Jennie Spotila Next week, the NIH will convene a peer review panel to evaluate and score the applications submitted under the Data Center and Collaborative Research Center RFAs. NIH’s management of conflict of interest is key to understanding who is – and who is not – on the