Action for M.E.
Action for M.E. takes action to end the ignorance, injustice and neglect faced by people with M.E. We do this by meeting need now to improve the lives of people with M.E. while taking action to secure change for the future.
Alongside providing information, support and advice to people to help improve their health and well-being, Action for M.E. works with professionals to enhance the care and support that people with M.E. receive and funds pilot research projects to advance knowledge of the illness.
Last updated:
05/10/2023
Claim status:
This is a Claimed organisation
Services
This is a Claimed service
We offer free support to families of children and young people with M.E. They do not need a diagnosis to use this service.
This is a Claimed service
We offer individually tailored whole-person care. Action for M.E. is committed to patient-led care, supported by robust biomedical evidence.
This is a Claimed service
Our free, friendly Information & Support service supports people with M.E., their carers and professionals to address the challenges presented by the illness.
This is a Claimed service
Action for M.E.’s M.E. Friends Online forum is the place to come for peer support and friendship if you’re over 18 years old. It is free to access.
This is a Claimed service
Peer support for young people under the age of 19 who have M.E. Volunteer peer monitors keep this a friendly and safe space.
This is a Claimed service
Our Young People's Counselling Service is available for young people, aged 13-18, with either suspected or diagnosed M.E. or Chronic Fatigue Syndrome
Contact information
You can use the information below to get in touch with Action for M.E.