The ME Association is not primarily a charity for children with M.E. but we are involved in helping to improve the current situation and we work with others to do so.
Below are key documents that attempt to explain what should be done for children and young people with M.E. They might be useful as background and to help when in discussions with healthcare professionals, schools, and social care providers.
Please note these are downloads. You can read them on-screen and save to your computer, phone or other device and can attach them to any email you might need to send. But you will need access to a printer if you wish them printed.