Featured
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.
Featured
A parent shares a heartfelt and honest look at life after getting a tough diagnosis for a child. It talks about the initial shock and the journey to finding a new normal. It highlights the importance of building a supportive community, adjusting to new routines, and trusting medical professionals. Discover the emotional ups and downs of getting unsolicited advice and comparisons from others.
6 Members of Young Epilepsy's Youth Voice Network attended the very first Youth Summit of the International Epilepsy Congress, hosted by the International Bureau of Epilepsy.
Read about our first ever CarFest, the UK's largest family fundraising festival in support of children's charities.
What happens when you transition from paediatric to adult epilepsy care?
When it comes to transitioning from paediatric care to adult care, what do you need to know, and what should you ask?
Meet inspiring Young Reps who raise epilepsy awareness, support peers, and share their experiences as part of the #EpilepsyTogether community.
Explore the #EpilepsyTogether initiative, empowering young people with epilepsy through support, community, and shared experiences
Fasting during Ramadan can be a challenging and sometimes fearful time for those with epilepsy, or other medical conditions. Miriam gives her advice on taking part safely, IF you feel you want to.
Roald Dahl nurses Liz and Bex discuss helping young epilepsy patients transition from pediatric to adult healthcare with guidance and personalized support.
