Press Release from the European ME coalition (EMEC): 'Scientists call for more European research on ME/CFS' Brussels, 10 June 2020 More than one...
The advocacy group of Evelien Van Den Brink and Francis Martin (of which I’m part) now has an official name and website. Check it out here:...
"Hi everyone! Time for an update: We have super important news! The Committee on Petitions is preparing a resolution on ME! This is the...
How to sign the EU-petition on a request for funding for biomedical research on Myalgic Encephalomyelitis (No0204/2019) 1) Go to the EU website:...
07/01/2020 - Agenda item, Petitions Committee P-05-926 To Provide a Chronic Fatigue Department in Wales P-05-926 To Provide a Chronic Fatigue...
Petition to stop contracting out DWP health-related benefits assessments and make the system fairer:...
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...
A young woman with ME has started UK Parliamentary petition seeking training in relation to ME for teachers: Staff training and mandatory support...
A friend on mine (Evelien) has succeeded in getting a petition on ME accepted by the EU Parliament [link below*]. The petition highlights the...
Scottish Petitions Committee discussion on M.E./CFS [MEDIA]
Station: Manx Radio and Aiir Date: April 18, 2019 WebRadio:...
UK Gov petition (ie at 10,000 Govt will respond) In a speech on 5/3/19, Work & Pensions Secretary Amber Rudd announced plans to merge assessments...
I realise this may be controversial but it goes into it quite deeply, maybe too deeply. I believe that "Melvin Ramsay's Myalgic...
Been asked to share this Spanish petition on social media but wondered if any of our Spanish speaking members could offer an opinion on the...
Hi everyone, greetings from Germany the situation here in Germany is still pretty bad, even some MPs are now familiar or at least involved with...
A conversation in the 'News from New Zealand and the Pacific Islands' thread led to the idea that 'we'* work together on ensuring that people with...
Parliament of Australia from the Minister for Families and Social Services, Mr Fletcher Thursday, 4 April 2019 Page: 87 Myalgic...
Spotted this on social media. HMD has noted a “paucity of research” on ME/CFS and that “more research is essential”; only 1% of the needed funding...
https://www.bbc.co.uk/news/uk-england-derbyshire-46880547 A debate has been held in parliament about a chronic pain condition after a petition...
https://www.change.org/p/increase-research-funding-for-me-cfs/u/23686254?cs_tk=AUWl2Qz7NG-fLViGA1wAnBKDWTbxtNsAD1IAIo2cXA%3D%3D&utm_campaign=8ea457...
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