At the ME Association, we believe that research holds the key to transforming the lives of people with ME/CFS and Long Covid. Since establishing the Ramsay Research Fund in 1989/1990, we've been committed to funding high quality biomedical research into ME/CFS. So far, we’ve invested £2.6 million into research — with another £2 million planned over the next three years. None of this would be possible without your continued support. Thank you for helping us make a difference! Find out more: https
At the ME Association, we believe that research holds the key to tran…
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About the MEA - The ME Association
About the MEA - The ME Association
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2.1K views · 63 reactions | Sajid Javid Secretary of State for Health & Social Care - ME/CFS Research Meeting The Department of Health and Social Care - DHSC has Tweeted a video about the Health Secretary, Sajid Javid 's Roundtable Meeting on the 9th of June 2022. TWEET: https://twitter.com/DHSCgovuk/status/1537759460818505728 See the MEA blog about this meeting here: https://meassociation.org.uk/sjgu #pwME #MECFS #MyalgicE #DHSC #GOVUK #ukgovernment | ME Association | Facebook
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Tomas et al. (2019) Assessing cellular energy dysfunction in ME/CFS using a commercially available laboratory test. Biomarker research is important because biomarkers—measurable biological indicators of disease—may help diagnose ME/CFS. This is one of several studies that needs replication before any firm conclusions can be made as to its accuracy and to ensure it is specific to ME/CFS. Read more about the study, funded by the ME Association's Ramsay Research Fund, here: https://www.nature.com/a
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4.5K views · 74 reactions | This month, the ME Association announced...
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ME/CFS is a life altering disease. Your support will fund crucial research into the energy crash in ME/CFS, and give hope to the hundreds-of-thousands with this devastating illness in the UK. Donate now, and have your amount doubled! https://meassociation.org.uk/BigGive2025 #MECFS #MyalgicEncephalomyelitis #LongCovid #BigGive2025 #ChristmasChallenge #WhenRestIsntEnough #DoubleYourDonation | ME Association
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ME/CFS is a life altering disease. Your support will fund crucial rese…
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216K views · 4.2K reactions | Dr Nighat Arif says on X (formerly Twitter): “ME is a debilitating disease. I know my patients struggle in getting support because the research and evidence base data is scanty - but I hope using the NICE -Myalgic encephalomyelitis (or encephalopathy)/chronic fatigue syndrome: diagnosis and management - helps provide guidance of what you are entitled to on the #NHS “ ⤵️nice.org.uk/guidance/ # #MEAwareness2025 | ME Association | Facebook
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Research and Training Opportunities
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