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Galway Premiere of the award winning medical documentary film 'Unrest' (97 mins) about Myalgic Encephalomyelitis (M.E). " The screening of Unrest will be preceded by a brief introduction and followed by a 15-minute Q&A session, where M.E patients will reflect on their experiences of being...

20/08/2017 "The Medical Research Council invites proposals under its cross-board highlight notice in the area of Chronic Fatigue Syndrome and Myalgic Encephalomyelitis. Proposals should address the mechanisms underlying chronic changes related to CFS and ME in one or more of the theme areas...

" Join the Institute for Neuro-Immune Medicine as we host, Unrest, the Sundance award-winning documentary about ME/CFS, the most common disease you've never seen. Jennifer Brea is about to marry the love of her life when she’s struck down by a fever that leaves her bedridden. When doctors tell...

9 November 2017 "Subject: Funding of research on ME/CFS Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) affects more than one million people within the EU. This illness is characterised by persistent and excessive fatigue, post-exertional malaise, flu-like symptoms and cognitive...

I still :inlove: Oystein Fluge

ah yes, it's all making more sense now

I think those can be read in quite different ways. I think from his perspective he is trying to show (a bit like Wessely et al) that these patients have been 'long neglected/not taken seriously' but in fact are all suffering from BDS and respond to his treatments. eta: if you watch Unrest, the...

David Tuller represents a lot of ME sufferers, its not only a few 'militants' who came up with the $60,000+ for him to continue his investigations. He is acting on our behalf and therefore according to the law: Action against discrimination You can do something voluntarily to help people with a...