November 13, 2015
Action for M.E. supports people affected by M.E. to live life to their full potential. We do this by providing a wide range of information and resources, and increasing awareness and understanding of the illness and its impact.
But of course it’s also vital for people with M.E. to have their own voices heard, in order to represent their needs for care and support. We’ve created a self-advocacy resource, Nothing about M.E. with me, to help you do just that.
This was launched at out AGM and conference yesterday, and addresses the needs of people with M.E. in England, as rights and entitlements can differ in the devolved nations. We will be building on this to ensure that we include information and signposting relevant to Scotland, Wales and Northern Ireland.