Childhood, Adolescence and Risk

But knowing about risks, discussing them with others (clinicians, family, teachers etc), and taking steps to reduce them, can help you navigate living with epilepsy.

Having a long-term condition like epilepsy doesn’t mean you can’t take part in everyday activities, but it does mean you might need to take some extra steps to make sure you keep as safe as possible.

Take a look at our Epilepsy Risks leaflet for key things you need to know:

PDF iconEpilepsy & Risk – Parent’s & Carer’s Guide

Moving from Paediatric to Adult services?

Developing independence as you get older is important, and living with epilepsy can make it harder to feel like others in your social group. Moving from paediatric (children’s) to adult epilepsy services happens at the same time as many other changes linked to being a young adult.

It is important to know how to balance gaining independence with managing risk, so you can make informed choices to help you stay safer:

Childhood Epilepsy and SUDEP

Each year approximately 1 in 1000 people with epilepsy will die suddenly with no obvious cause of death found. This is called Sudden Unexpected Death in Epilepsy (SUDEP). The risk of this happening to children with epilepsy is lower than adults, approximately 1 in every 4,5000 children with epilepsy die each year. This risk increases if they have a more complex, rare form of epilepsy for example, Dravet Syndrome.

This is something you should be aware of and discuss with your clinician who can discuss your child’s individual level of risk (which varies between people with epilepsy).

This leaflet gives a summary of key information:

PDF iconSUDEP – Parent’s & Carer’s Guide

Further information on SUDEP can also be found here

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