Blogs
Here you will find tips, opinions, and info on different topics
Discover real experiences of tonic seizures from young people and families. Learn what they feel like and how to support someone through them.
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 Meadow's journey with epilepsy, from diagnosis to finding community support through Young Epilepsy. Help others facing epilepsy find hope and resources.
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.
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.