Welcome to the DSF Family Network!
The DSF Family Network is open to any parent/legal guardian or sibling and is interested in accessing our advocacy services and programs. Sign up below to be a part of this family community and to stay up to date on new advocacy resources, clinical trials, and educational and fundraising events.
Other community members who are interested in learning more about Dravet syndrome, supporting our community of families, and staying up to date on events and research are encouraged to sign up for our mailing list.
**Please note many of our programs are currently only available for families in the U.S. We invite you to check this list to see if there is a Dravet syndrome organization in your country who may offer additional resources.