Hello
For anyone on here who has a child with M.E./CFS, we would just like to let you know that the revised and updated version of our booklet, Your child and M.E., is now available.
Covering topics including symptoms, treatment, education, family matters and benefits, the booklet was developed with the Association of Young People with M.E. plus parents and healthcare professionals, to provide information and share ways of coping.
You can read it and/or download it free from our publications section or order a paper copy by phone.
We have a Support Line for anyone affected by M.E., including carers and family members, who need someone to talk to. Call Mon to Fri 11am to 3pm on 0845 123 2314 or email [email protected].
And we?ve just launched our carers forum, specifically for those caring for someone with M.E. Take a look at here.
Hope this is helpful
Best wishes from the Action for M.E. team