Receiving a diagnosis of Dravet Syndrome can be a frightening experience. Its important to remember you are not alone - other families are going through similar experiences. We have gathered together a number of written stories and videos from our Dravet Syndrome UK community. Always remember that, even though their symptoms and experiences may be similar, every child or adult living with Dravet Syndrome is different and can present differently.
If you’re interested in sharing your own Dravet Journey, click here to find out more.
Hannah had her first seizure at 3 months old. Now a young adult, her Mum Kelly, shares more about the challenges they've faced and the transition from children's to adult services.
Tate had his first seizure at just 7 weeks old. His parents, Paul and Jade, share their story.
Calla-Rose had her first seizure at 8 weeks old. Mum, Nicki, tells their story and Dad, Lee, encourages others to reach out for support.
Charlotte is 25 years old and lives with her mum, Julie. She was diagnosed with Dravet Syndrome at 10 years old.
Penny lives with her parents, Carrie and Adam, sister Ruby and brother Teddy. She had her first seizure, which lasted for 13 minutes, at 6 months old.
Emily had her first seizure at 4 months old. Her parents Catherine and Gareth, share more about 'coming to terms' with the diagnosis of Dravet Syndrome.
Finn had his first seizure at 16 weeks old. Mum, Helen, tells their story.
Paige had her first seizure at nine months old. It lasted for 4 and a half hours. Mum, Gemma and Dad, Martin share their story.
Frankie had his first seizure at 6 weeks old, lasting over an hour. Mum, Stacey, shares their story.
