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.
Find out how Faye found solace in swimming after her epilepsy diagnosis, and how she recommends exercise to anyone with epilepsy.
Learn how to maintain a healthy balance between exercise and managing epilepsy, with tips for safe physical activity and overall well-being
Read Olivia’s experience with the ketogenic diet for managing epilepsy, sharing how it helped her take control of her health.
Read Jasmine's personal story about overcoming anxiety, learning coping strategies, and finding balance in life while living with epilepsy
In her blog, Livvy talks about having seizures at night and what she does to try and make her life with epilepsy easier.
“Just man up and deal with it”, that's what they all say? Renell shares his experience of mental health and epilepsy.
Discover Jack's experience with night-time seizures, sharing his challenges and insights on managing this aspect of living with epilepsy.
Help make the night before Christmas magical for all children.
We’re asking young people to tell us how their experience of epilepsy care has changed as they’ve gotten older. The survey will help us understand what information or support young people might like to receive, as well as how healthcare for young people with epilepsy can be improved.
Zac had his first seizure, just aged 2. His parents describe their journey from then, until his diagnosis and beyond.
