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 reviewed:
05/10/2023
Claim status:
This is a Claimed organisation
Services
This is a Claimed service
We are here for parents or family members of a child or young person with the symptoms of M.E., CFS or post-viral fatigue syndrome; they don't need to have a confirmed diagnosis. We can:
1. share key...
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 friendly Information & Support service can support anyone affected by M.E. of any age by phone and/or email.
We can help break issues down so they feel less overwhelming, and explore prioriti...
This is a Claimed service
Online peer support forum which is open to anyone aged 18 or over affected by M.E. It offers friendship and fun.
We hope you enjoy using the forum and find it helpful.
Our online forums ask you t...
This is a Claimed service
Peer support for young people under the age of 18 who have M.E. Become a member of the fun and friendly forum. Volunteer peer monitors keep this a friendly and safe space.
If you’re under 16, you’ll ...
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.