If you are a child or young person with M.E., this section of the website is just for you and your family. We want to make sure you have the information you need about M.E. so that you can make decisions about living with M.E. in the way that works best for you.
If you have a question about symptoms, seeing a doctor, going to school, or any other aspect of living with M.E. that isn't answered on these pages, you can ask one of our Information and Support Officers.
In April 2017, we will launch two new forums for Action for M.E. Members - one for under 18s, and one for parents/carers of children and young people with M.E. Watch this space!
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