Blogs
Here you will find tips, opinions, and info on different topics
Discover real experiences of absence seizures from young people and families. Learn what they feel like and how to support someone through them.
Discover real experiences of myoclonic seizures from young people and families. Learn what they feel like and how to support someone through them.
Discover real experiences of tonic seizures from young people and families. Learn what they feel like and how to support someone through them.
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.
Rachel tells the story of how her son Charlie was diagnosed with Lennox-Gastaut Syndrome, and how her family is looking forward.
Discover real experiences of focal seizures from young people and families. Learn what they feel like and how to support someone through them.
Help us improve resources for newly diagnosed children and young people with epilepsy. Donate to our Christmas appeal today.
A parent shares a heartfelt and honest look at life after getting a tough diagnosis for a child and the initial shock and the journey to finding a new normal. The letter highlights the importance of building a supportive community, adjusting to new routines, and trusting medical professionals.
Discover Osiris' journey with epilepsy and learn how vital support, resources, and information can make a difference for newly diagnosed children.
Discover Lexi's epilepsy diagnosis journey, told by her mum Sarah, and how vital support from Young Epilepsy can make all the difference.