CPN | Dravet Syndrome

Dravet Syndrome

Dravet Syndrome is a rare genetic dysfunction of the brain and presents as intractable epilepsy. Dravet is a lifelong condition that begins in infancy, typically in the first year. Children with Dravet may develop a number of seizure types and developmental delays that severely impede their quality of life.

For more information, visit Dravet Syndrome Foundation.

CPN’s NeuroJourney tool will help orient and support you as you navigate the ever-evolving needs of your child and the complex decisions that lie ahead.