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.
Claim status:
Claimed
Last reviewed:
28/10/2022
Services
We offer individually tailored whole-person care. As well as listening and caring for the needs of the whole person, we offer encouragement and support to families and the immediate community of carers. We...
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 priorities a...
Our free, independent one-to-one advocacy service supports adults living with a confirmed diagnosis of M.E. We provide issues-based independent advocacy support for adults with a diagnosis of M.E./CFS on a...
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...
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...
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...
Contact information
You can use the information below to get in touch with Action for M.E.