Blogs
Here you will find tips, opinions, and info on different topics
Paige shares how dignity, understanding and quick, calm support during seizures helped her feel safe and included, and what every school needs to get right.
Having epilepsy since infancy, Emma is now seven years seizure-free and a dedicated advocate for young people who lack community.
Dian explains why Purple Day matters, sharing their experience of epilepsy at school and how speaking up builds awareness, kindness and confidence.
When her daughter Neli was diagnosed with epilepsy, Alwen turned hope into action—raising £1,200 through Young Epilepsy’s Walk 100 Miles Challenge. Join her journey
Sam found strength through marathon training after her daughter’s epilepsy diagnosis, raising £3,000 and hope with Young Epilepsy’s support.
Discover why Jack ran the London Marathon for his brother Sam, raising £750 for Young Epilepsy and showing love, support, and hope through every mile.
After her epilepsy diagnosis, Becca has used her lifelong passion for poetry and performance to develop tools for living with her condition. Read her story.
Laura's journey took her from a place of isolation living with seizures to becoming seizure-free and helping adults with learning difficulties.
From 30 seizures a day to living life fully – discover Liberty’s remarkable epilepsy journey and the breakthroughs that changed everything.
Miles is seizure-free and lives life to the full. Getting here, however, was an inspiring journey to overcome the pressures and triggers of alcohol and drugs.