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Dravet Syndrome

Dravet Syndrome Awareness

Understanding Dravet Syndrome is essential to Paige's Promise mission. Knowledge creates compassion, and compassion builds community.

What is Dravet Syndrome?

Dravet Syndrome is a rare and severe form of epilepsy that typically begins in the first year of life, often with seizures triggered by fever. It is frequently associated with developmental delays, sleep difficulties, and other challenges that can affect a person throughout life.

Most cases are caused by a change in the SCN1A gene, though other genetic causes exist. Dravet Syndrome does not go away with age, and there is currently no cure. Care focuses on reducing seizure frequency, supporting development, and improving quality of life.

Resources and Research

Resources and Research

These organizations offer reliable information about Dravet Syndrome, current research, and support for families.

Family Support

Caring for a child or adult with Dravet Syndrome often involves a team of specialists, including neurologists, therapists, and educators, working alongside family and caregivers.

Connecting with other families, advocacy organizations, and support networks can provide practical help and a sense of community for those affected.

A note on medical information

Medical disclaimer

This page provides general information about Dravet Syndrome and is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider for medical questions or concerns.