Blogs
Here you will find tips, opinions, and info on different topics
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.
Follow Rachel’s journey from epilepsy diagnosis to finding support and understanding, sharing her insights and resilience along the way.
Follow Daisie's rare epilepsy journey & how her family copes. Learn about STXBP1 gene, challenges, and Purple Day's impact. Join us in supporting kids like Daisie!
From the heartache of 20 seizures a day to the triumph of taking those first steps. Bodhi's journey is a reminder that with support, anything is possible..
Livvy was diagnosed with Autism just after her 18th birthday. In her blog she discusses how she always 'felt different' and calls for greater understanding towards autism.
Explore a personal journey with ketogenic diet therapy for epilepsy, highlighting the challenges, adjustments, and positive impacts on health.
Read Emma's story of being diagnosed with epilepsy, her emotional journey, and the support she found along the way to manage her condition.
A personal story by Alice, telling 5 things she wishes she had known when she was diagnosed with epilepsy.
Learn about the impact of medication toxicity in epilepsy, including signs, symptoms, and ways to manage treatment safely.