Welcome to AYME
The Association of Young People with ME (AYME) is a UK charity that provides support for children and young people aged up to 26 who have ME/CFS. AYME is also here to help and support parents, carers and professionals in health, education and social care.
This site shares some of the wide range of information and experience we have available, including features on health, education and real life accounts from young people with ME/CFS.
FOR HELP & INFORMATION CALL 0330 2211223
If you are a registered member, but have forgotten your username please email email@example.com with your full name and they will be able to help you.
Not an AYME member yet, or need to re-register?
Join FREE today
M.E. Awareness Week 2015 Find out what's going on this year and get involved!
AYME's Chief Executive, Mary-Jane, meets Prime Minister David Cameron! Read about Mary-Jane's impromptu meeting with the UK leader.
Take part in the Great North Run for AYME! The next GNR is in September this year. Email firstname.lastname@example.org to sign up!
Get involved this ME Awareness Week with a #nowyouseeME selfie!
New ME/CFS research announced To find out more and to read Dr. Esther Crawley's comments, take a look at AYME's article.
AYME's book, Forget ME Not, now available to purchase Click on the link to find out more about the collection and to buy it for only £6.99!
Join our campaign for the run-up to the next General Election NOW!
Members, parents and carers - please write to your MPs using the template letters (downloadable below), and help AYME to get your voices heard on behalf of all of the children and the young people in this country affected by ME/CFS.
The forthcoming election in May 2015 is an opportunity for us all to shout about the lack of services and understanding of the condition throughout the UK.
New! AYME Supporters: for friends and professionals and all those who wish to support AYME in the work we do and receive news, research and fundraising updates.
Re-launched! Parents and Carers (previously LINK): AYME understands that being a family member of a young person with ME/CFS comes with its own set of challenges. That's why we set up the Parents and Carers group, to equip you with the support and information you need, every step of the way.
To find out more and join here
AYME is collecting members' stories, and the ones we've received so far are truly inspiring. We hope that they bring hope to young people, and to their families and supporters. You can share your own story by emailing email@example.com to ask for a template.
Read the stories we have collected so far here.