Dravet Syndrome UK

Dravet Syndrome UK was created in 2008 by a group of parents who came together looking for support, resources and information relating to a rare, little known neurological condition called Dravet Syndrome. Today, our database has grown to over 500 families across the UK. We are an independent charity and the only UK organisation dedicated to improving the lives of those affected by Dravet Syndrome. Dravet Syndrome is a complex and devastating condition. Living with a child or adult who has Dravet Syndrome can be a very difficult and potentially isolating experience for families. From a medical perspective, there is an urgent need for more research into the causes and complexities of the condition, in order to identify more effective approaches to diagnosis and treatment. Our mission is to bring hope to families living with Dravet Syndrome through support, education and medical research. To fund medical research into Dravet Syndrome. To raise awareness within the medical community. To support families affected by Dravet Syndrome.

Funding medical research. providing medical equipment. Organising medical/family conferences. Organising and providing family holiday grants. Distribution of information.