What is Dravet Syndrome?

Dravet syndrome, also known as Severe Myoclonic Epilepsy of Infancy (SMEI), is a rare form of intractable epilepsy that begins in infancy and proceeds with accumulating morbidity that significantly impacts individuals throughout their lifetime. It has an estimated incidence rate of 1:15,700. [1]

Community. Research. Progress.

Raising Hope & Changing Lives through Research

The mission of Dravet Syndrome Foundation (DSF) is to aggressively raise funds for Dravet syndrome and related epilepsies; to support and fund research; increase awareness; and to provide support to affected individuals and families.

We know that the fight against Dravet syndrome will never be successful without teamwork. None of us can do this alone and to achieve great things we must work together.

Thanks to the collective efforts of our community, DSF has achieved numerous milestones to celebrate. Become a part of #TeamDSF by donating, launching a personal fundraising campaign, or exploring other ways to give.

DSF Recent News & Information

Keep up to date on current information that is important to you in our weekly Decoding Dravet Blog posts and through our email updates.  

How Community Support Drives Progress in Dravet Syndrome

Discover how community support has driven progress in Dravet syndrome research, family programs, and hope for a cure through DSF’s grassroots efforts.
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How Research Changed the Way Dravet Syndrome Is Treated — and What Comes Next

Since DSF was founded in 2009, research has helped move the field toward more informed, Dravet-specific care.. Learn how community-powered progress has shaped today’s treatment ...
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Purple Drives Progress

This June, purple is more than a color. It’s a movement. It’s hope in action. It’s families, advocates, friends, and supporters coming together to move ...
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Upcoming Events

Want to get involved? Join an Event? Host an Event? There are so many ways you can support DSF! View all of our upcoming events here

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