Closure Alert:
Hundreds of children and young people across Surrey and
Hampshire are set to lose specialist NHS CFS/ME services as the
Frimley-based CFS/ME specialist consultant and specialist nurse are not
replaced.
We urge all parents to raise this issue with their MP.
Click here for sample
letters.
BioMedical research into ME
Please sign a new government petition for more biomedical research into the causes of ME. You can sign the petition
here.
Study warns of higher ME/CFS rates among pupils
Far more children than previously thought miss schooling because of CFS/ME.
New research findings by Dr Esther Crawley, AYME's medical advisor, hit the
headlines.
To see AYME's CEO and young person, Rebecca Miller on BBC Breakfast go to:
BBC News
Do something amazing
AYME’s fundraising team can help you organise a successful fundraising event or a get sponsorship for doing something
remarkable or achieving a life-long challenge. See our new set of eye-catching fundraising event posters
click here.
Hello! Welcome to AYME,
AYME(pronounced ‘aim’) is the largest charity for children and young people with ME/CFS, with over ten years of knowledge and experience
about how this illness affects children and young people.
We know how important it is to have good, understanding friends, which is why AYME
offers lots of friendship-supporting services like an online community, pen pals, e-mates, buddies and local get-togethers, all run by other
young people with ME/CFS. They are all under 26 and have probably been through similar situations as you. Members get a bi-monthly magazine
packed with young people’s news and views. You can choose to get involved or just enjoy reading and listening to what others are getting up
to.
Join online here! It’s
absolutely FREE for anyone up to 26 in the UK and now our membership form is online you can join quickly and easily and get even faster
access to all of our services.
New to the site? If you're not quite sure where to start, we have a short guide to articles you might find useful to get you going!
Parents and carers can speak to our experienced and knowledgeable staff on the phone on 08451 23 23 89,
email us or join AYMElink, our parents and carers
support group.
Health, education and social care professionals are also welcome to contact us. We offer information and training sessions and are keen to
share our experience and knowledge about ME/CFS and children to increase recognition and understanding. Please call us on
08451 23 23 89, email us or join AYMElink
as a professional.
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