Blogs and Stories

A young man smiles as he tends his garden.

Epilepsy is part of my story – but it doesn’t define me

4th April 2026

Adam’s journey with epilepsy shows resilience and hope—overcoming setbacks through creativity, nature, and support networks to inspire new beginnings.

I’ve found purpose through my pain

17th March 2026

Emma-Louise turned trauma from epilepsy, bullying and loss into hope—writing a book to support others and raise awareness through Jo’s story.

A young woman sits on the step of a doorway, surrounded by baskets of pink flowers.

I want to be the advocate I never had

17th February 2026

Having epilepsy since infancy, Emma is now seven years seizure-free and a dedicated advocate for young people who lack community.

A mother and daughter smile in a selfie.

Why I ran the Manchester Marathon for Young Epilepsy

20th January 2026

Sam found strength through marathon training after her daughter’s epilepsy diagnosis, raising £3,000 and hope with Young Epilepsy’s support.

Laura, a young woman, smiles in a wedding dress from a vehicle.

I’m seizure-free and helping others

16th December 2025

Laura's journey took her from a place of isolation living with seizures to becoming seizure-free and helping adults with learning difficulties.

A woman and two boys smile widely in Christmas jumpers.

I had epilepsy - now I’m raising two sons with it

2nd October 2025

Discover the story of Jo, Rafferty, and Fin, a mother and two sons who have had an epilepsy diagnosis, and be inspired by their journey this Christmas.

A young woman holding pride flags smiles next to a dog on a sunny day.

Charlotte’s Update: Results Day Rejection to Dream Career

27th August 2025

Charlotte's epilepsy diagnosis at 18 compromised her A-levels, but perseverance and openness to support led her from rejection on results day to her dream job.

I am Jasmine

18th July 2024

Meet Jasmine, one of the heroes of our #UnderstandMyEpilepsy Campaign. Jasmine is 18 and experiences prolonged tonic clonic seizures. ForJasmine, this has meant that her teachers and students at school don't understand her epilepsy and the challenges that she faces.