For too long Myalgic Encephalomyelitis (ME) has been known as an ‘invisible illness’ with sufferers left with little support and no medical way forward. Across the globe there are millions who live with the condition, and with the knowledge that there is no cure. Those millions feel that they are completely absent from the active lives they could have been living. To raise awareness of the condition and the desperate need for a medical breakthrough local charity, Hope 4 ME and Fibro Northern Ireland, joined together with support groups across the world recently to lobby governments to better recognise the condition and its devastating impact.
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