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Patient Families – Help Shape the Future of DSF!
At DSF, our mission is to aggressively raise funds for Dravet syndrome and related epilepsies; to support and fund research; increase awareness; and to provide ...
Caregiver Connect – DSF’s Newest Resource
As a caregiver for a child or adult with Dravet syndrome, it is normal to have feelings of anger, depression, and resentment. The emotional role ...
Thank you to our Departing Board President and Welcome to our New Board Member
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; ...
Mark Your Calendar for our 2024 Conference!
We are pleased to announce that the 2024 DSF Biennial Family & Professional Conference will be held next year in Minneapolis, Minnesota, on June 20-22. ...
Get Involved in Advocacy for Dravet Syndrome
Last month, I had the opportunity to attend Rare Disease Week on Capitol Hill with the EveryLife Foundation for Rare Diseases. This event was a ...
COVID-19 Vaccination and Dravet Syndrome
In 2020 the COVID-19 pandemic completely disrupted the lives and health of the United States and the world. The development of vaccinations against COVID-19 were ...
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