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 M.E./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 M.E./CFS.
FOR HELP & INFORMATION CALL 0330 2211223
If you are a registered member, but have forgotten your username please email firstname.lastname@example.org with your full name and they will be able to help you.
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|AYME is a registered charity 1082059, company registration 03981646.|
Privacy and Data Protection
AYME exists for its members, who are young people and children. To ensure the protection of these members, their families and/or carers, every effort is made to maintain the security/accuracy of any data held and to monitor the integrity of the advice and support given by AYME. AYME is registered under the Data Protection Act, no. Z9020055
Please be aware that cookies are in use on this website. Please disable these if you do not want them stored on your computer as they contain user information. Please refer to your ‘Help' menu or visit: www.allaboutcookies.org Note: this may affect your access to the members' area and message board.
Please contact the AYME office on 01908 379737 for a copy of the DP Policy Statement. More DP information on: www.ico.gov.uk/what_we_cover/data_protection.aspx
The 2015 UK CFS/ME Research Collaborative Conference for researchers and Associate members takes please on Tuesday 13 and Wednesday 14 October in Newcastle. For information about delegate attendance and registration: More info
AYME Spotlight Tour is Launched! Our charity is going on the road, and we can't wait to meet you! Have a read about AYME's plans to tour the UK, starting this year.
For friends and professionals and all those who wish to support us in the work we do; and receive news, research and fundraising updates.
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.
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 email@example.com and ask for a template.