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
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At the ME Association, we believe that research holds the key to tran…
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This year, we are doing the BigGive to fund a new research study - but what is this study about? And how it may help the ME/CFS community? Watch our latest video to learn all about this worthwhile study, and how your donations next week will make a huge difference! Register for a reminder to donate here: https://meassociation.org.uk/big-give-2025/ #Donate #pwME #MECFS #MyalgicEncephalomyelitis #PEM #PostExertionalMalaise #MyalgicEncephalopathy #MECFSResearch | ME Association
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The amount of people that confuse chronic fatigue with chronic fatigue as a syndrome MECFS -it’s actually really frustrating and dangerous to us getting more support and research in place. People are belittling a multi system complex condition -there isn’t a cure and if there was you wouldn’t be charging people for it you’d be shouting it from the rooftops and to the World health organisation and the ME association. There’s also the problem of GP’s misdiagnosing and not having training in chroni
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ME/CFS is a life altering disease. Your support will fund crucial rese…
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