A New Non-Profit for ME & CFS Comes Online
The American ME and CFS Society is live, and we need your participation!
The American ME and CFS Society is live, and we need your participation!
Dr. Faith Newton, Deleware State University, has created several resources to help children with ME/CFS improve their educational outcomes including the newest piece, a sample physician’s letter.
#OMFScienceWednesday showcases Dr. Jonas Bergquist.
What is Personalized Health? – How researchers are using personalized health to understand ME/CFS
Tuesday 24th Oct., 2017 will long be remembered as a significant day for anyone involved in ME politics.
The Solve ME/CFS Initiative (SMCI) announced the recipients of the 2017 Ramsay Award Program on Tuesday. The Ramsay Award Program, now in its second year, is a competitive grant that funds ME/CFS researchers at every stage of their careers. The five winning proposals receive one year of funding to research a diverse range of topics including immunology, bioenergetics, metabolomics, microbiome and neuroendocrine biology. The awardees hail from six different countries across the globe.
Learn about science that OMF is supporting. Follow OMF on Facebook and Twitter.
The Solve ME/CFS Initiative (SMCI) held its second annual Discovery Forum Saturday October 14. The forum dubbed “a new era in ME/CFS research” brought together leaders from academia, government agencies, private clinics, biotech and research institutions to discuss developments in the field of ME/CFS research.
Keep up-to-date on this issue by following the Twitter accounts @mecvsnieuws and @ME_gids More than 10,400 signatures for the Dutch petition ‘ME is not MU(P)S’ (Medically Unexplained (Physical) Symptoms) was presented to Prof. van Gool, president of the Dutch Health Council three weeks ago on September 18th. The petition aims to hold the Dutch Health Council
OMF expands international outreach. Corrected link to the translation page.