Let's assume that the EU decides to make €2 million available for ME/CFS research and projects. What would be the best way to spend this money?
News about Evelien's testimony to Parliament has already been posted on the thread about the EU Petition but I thought the testimony deserved its...
So the big European MS meeting just finished a couple of days ago. The scientific program book is 131 pages long for a three day meeting!!...
A friend on mine (Evelien) has succeeded in getting a petition on ME accepted by the EU Parliament [link below*]. The petition highlights the...
[MEDIA]
The Brain, Mind and Pain (BMP) initiative has today launched its updated Book of Evidence for the 2019-2024 EU mandate. This Book of Evidence...
Note from Moderators: IiME created the EMEA, and also the EMECC (Clinicians Council) and the EMERG (Research Group). The EMEA is a member of EFNA...
Hi I've managed to get three (written) European Parliamentary questions asked on ME/CFS: Alex Mayer (S&D) Reference :E-006901/2017 Rory Palmer...
A European Research Agenda for Somatic Symptom Disorders, Bodily Distress Disorders, and Functional Disorders: Results of an...
What's the one research problem you'd like European countries to fix and why? This could be solving a problem for society or improving the way...
The European Union is planning to spend €100 billion (US$120 billion) on its next major research-funding programme, for 2021 to 2027 — a...
The European ME Alliance has been a member organisation of the European Federation of Neurological Associations since 2015...
"Currently, 11 percent of EUR’s professors are female. Women are still underrepresented in the top echelons of science. As a result, they miss...
[ATTACH] 9 November 2017 "Subject: Funding of research on ME/CFS Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) affects more than...
I realise that this is the community lounge and it may be hard to drag people away from Betty's bar but I have a very short memory span and...
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