Better futures for young lives with epilepsy and associated conditions

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Meet the people you help

Don't take our word for it, hear from the people we have helped thanks to you.


Richard's mother Vic, tells us about her son's epilepsy and how they found support through Young Epilepsy

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"Young Epilepsy's helpline was our lifeline." Lisa explains how our national helpline has supported her from the point of her son's diagnosis through to his transitioning to university.

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Siobhon, mother to brave 22-month-old Arla who lives with Dravet Syndrom, uses our App to track seizures and appointments.

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youngepilepsy RT @ChairEpilepsy: Olivia’s story featured on @youngepilepsy’s #ThisIsEpilepsy appeal is compelling, yet, her story isn’t an isolated case.…
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youngepilepsy @SallieannGould Thanks Sallieann. It's not our survey but we'll certainly pass on your feedback.
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In the UK, 70% of the population with epilepsy could be seizure free with the right treatment.

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Cyber EssentialsFundraising RegulatorYoung Epilepsy is the operating name of The National Centre for Young People with Epilepsy (NCYPE).
Registered Charity number 311877 (England and Wales)

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