We help people with ME/CFS to understand and survive their illness
Story
I was diagnosed with m.e/ cf three years ago. And I know that more research and development is needed. To help find a cure for this terrible debilitating illness.
The more money raised, the less likely it will be, that people will have to fight to get acknowledged that they are actually ill.
The ME Association campaigns hard to get ME recognised as a severe neurological illness. Our helpline provides essential information and support to adults and children who have ME/CFS, and to their families and carers. We also fund biomedical research into the physical nature and causes of ME/CFS.