We support people living or caring for someone with Myalgic Encephalomyelitis (M.E., sometimes called chronic fatigue syndrome or M.E.CFS) of any age, anywhere in the UK.We offer a range of free services by email and phone, including our Information and Support Service; a Listen to M.E. helpline for anyone who just needs to talk; independent Advocacy services fr adults and for children and young people with M.E.; Family Support for parents and loved ones of children with M.E.; and online peer-support including online forums for adults and young people with M.E. We also offer individually tailored whole-person care from our Healthcare Services team. 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.
People with M.E. of any age, anywhere in the UK, and their families. We also offer information and resources for professionals.
Oes - Free membership for children and young people (Under-18s) Parents can join as supporting members of Action for M.E. for £21 a year, this will give them access to the members-only parents forum, our member’s magazine InterAction, info on education, health, fundraising news and much more!
Yes, anyone can contact us directly
42 Temple StreetKeynshamBristolBS31 1EH
https://www.actionforme.org.uk/children-and-young-people/introduction