Blogs
Here you will find tips, opinions, and info on different topics
Discover real experiences of myoclonic seizures from young people and families. Learn what they feel like and how to support someone through them.
Read about what atonic seizures really feel like, with honest stories from young people, families, and the UK epilepsy community. Share your own experience!
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.
Discover Lexi's epilepsy diagnosis journey, told by her mum Sarah, and how vital support from Young Epilepsy can make all the difference.
Receiving a diagnosis of epilepsy can come as a shock, leaving families feeling frightened, lonely and overwhelmed. Children and young people need help and support understanding their new diagnosis and how it will impact their lives. Help provide the support children need when they need it most.
Discover Meadow's journey with epilepsy, from diagnosis to finding community support through Young Epilepsy. Help others facing epilepsy find hope and resources.