we are your community
Every 18 minutes…
someone new is diagnosed with epilepsy.
Even before diagnosis is confirmed life changes.
Adapting to this new reality is tricky but with the right support many people can still live full lives.
Supporting the community
There are many ways to get support in the epilepsy community.
Epilepsy Action’s trained advisors can talk you through our services or provide the answers and resources you need.
Speak to our experts today
Show your support for the epilepsy community!
Stories from our community
Miles, marathons and moving stories: The extraordinary dads making a difference this Father’s Day
Emily Stanley | This Father’s Day, four dads share what it’s like seeing their children live with epilepsy and the things they’re doing to make…
Missing memories: Epilepsy Action shares National Epilepsy Week awareness campaign
Lisa Greer | This National Epilepsy Week, Epilepsy Action is highlighting an issue many people with epilepsy experience: losing precious memories of once-in-a-lifetime moments.
Who is 2026 Miss GB Surrey contestant Emma Dearling?
Emily Stanley | With Epilepsy Action supporter Emma Dearling beginning a new venture as a contestant on Miss GB Surrey, we share six amazing facts…
Living with epilepsy
Having epilepsy can have an impact on many parts of your life.
We have advice and information on everything from driving to planning a family.
Get involved!
You can make a difference for people with epilepsy.
Whether you want to donate, fundraise with us or volunteer your time, here are ways you can support our work.