Action for M.E.
Our vision is a world without Myalgic Encephalomyelitis (M.E.). Our mission is empowering people with M.E. to fulfil their potential and secure the care and support they need, while working towards a greater understanding of the illness and ultimately a cure. Alongside providing much-needed support services, we work closely with professionals and policy-makers to improve access to appropriate care and support services, and collaborate with scientists, patients and clinicians to drive forward biomedical research into M.E.
We are here for anyone living with or supporting someone with M.E. of any age, anywhere in the UK. You are not alone.
Contact us for free information, support and resources about any aspect of M.E., or to set up an appointment with our free Advocacy service for adults and young people; or our Family Support service for parents. You can also join one of our free online peer-support forums.
We also offer Healthcare Services for M.E. Our clinical includes a doctor, physiotherapists, counsellors and chaplains, offering individually tailored whole-person care. As a charity, we charge fees for our Healthcare Services only to cover our costs, and a bursary for up to 50% of fees may be available, depending on your circumstances.