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.


Monday to Friday, 10am - 2pm

If you are a registered member, but have forgotten your username please email onlineservices@ayme.org.uk 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

Already a Parent & Carer Affiliate (Link Member)?
Need to renew for 2015? R
enew here






     AYME is a registered charity 1082059, company registration 03981646.






AYME in the Sunday Express: 'ME parents' fury at child abuse claims'

NEW Scotland Leaflet 

NEW GP Leaflet 

NEW Education Fact Sheet 

Nearly 95% of children and young people with M.E./CFS have had their illness disbelieved 
Read AYME's official press release for ME Awareness Week 2015.

Take part in the Great North Run for AYME! 
The next GNR is in September this year. Email events@ayme.org.uk to sign up!

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!

Write to your MP

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.

Find out more about our General Election Campaign

Letter to MPs from Members

Letter to MPs from parents/carers


New! AYME Supporters: for friends and professionals and all those who wish to support us in the work we do; and receive news, research and fundraising updates.

Re-launched! Parents and Carers (previously LINK): Being a family member of a young person with ME/CFS comes with its own set of challenges, which is 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


Please do share your stories and experiences with us. Those we've received so far are truly inspiring, and can bring hope to young people, and their families and supporters. Email pr@ayme.org.uk and ask for a template.

Read the stories we have collected so far here.