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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.
Real Life Stories: Living as parents of a child with epilepsy. Lisa and John discuss their experience of being the parents of a child with epilepsy. Their son, Owen, now 21, was diagnosed at the age of 6. Read their story here.
St Piers School and College are proud to be working with AET to deliver the AET post 16 programme in West Sussex and Kent.
Young Epilepsy have recently been working alongside Emmerdale on Liv's epilepsy storyline, to raise awareness of how epilepsy affects young people.
The #FacingEpilepsy campaign
A big thank you to Total Merchandise for donating 110 hi-vis vests for our students at St Piers that took part in Road Safety Week on November 18th - November 24th.
Young Epilepsy welcomes decision on CBD treatment for children with epilepsy
At first a diagnosis of epilepsy can be scary and upsetting, especially for young people.
New Ofsted guidance highlights medical conditions as a safeguarding issue
The Tandridge Together Lottery is an exciting weekly lottery that raises money for Young Epilepsy and other good causes in the Tandridge district.
It's National Epilepsy Week!
