News & Updates

Dravet Syndrome Foundation is a non-profit organization dedicated to aggressively raising research funds for Dravet syndrome, a rare and catastrophic form of epilepsy beginning in childhood, and related conditions. By offering research grants for syndrome-specific research with a novel approach, DSF can move researchers and the medical community forward to find better treatments and a cure while assisting afflicted individuals and their families.

the foundation

Upcoming Events


junDravet Syndrome Awareness MonthMonth Long Event (june)(GMT-04:00) View in my time

junFight for a Cure Fundraising EventMonth Long Event (june)(GMT-04:00) View in my timeEvent Type :Virtual Fundraising Event

15junAll DayDravet Remembrance Day(All Day: tuesday)(GMT-04:00) View in my time

23junAll DayInternational Dravet Syndrome Awareness Day(All Day: wednesday)(GMT-04:00) View in my time

24junAll Day26DSF 2021 Virtual Conference(All Day)(GMT-04:00) View in my timeEvent Type :Educational Event

30jun11:00 am12:00 pmEducational Session: Caring for a Loved One with DEE and Dravet Syndrome: Harnessing the Power of Knowledge to Enhance Diagnosis, Reduce Seizures, and Improve Overall Quality of Life for All11:00 am - 12:00 pm(GMT-04:00) View in my timeEvent Type :Educational Event


24jul7:00 pm8:00 pmParty in your PJs for Dravet7:00 pm - 8:00 pm(GMT-04:00) View in my timeEvent Type :Fundraising Event,Virtual Fundraising Event

What is Dravet Syndrome?
Click here to learn more about Dravet syndrome and childhood Epilepsy
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Dravet Syndrome Stories

Meet our superheroes who fight every day against Dravet!

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Find out why Dravet Syndrome Research is our hope for a cure
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Get Involved

Find out how to help us in the fight to cure Dravet syndrome

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