DSF Legislative Advocacy
DSF is actively tracking legislative developments to anticipate any potential impacts on our patient community and to keep our stakeholders well-informed. We need your help to advocate for critical issues and policies that directly impact the Dravet syndrome patient community and others affected by rare diseases. By lending your voice, you can help drive meaningful change, influence decision-makers, and improve the lives of those living with these conditions.
Click on an image below to explore specific legislative updates and, when available, opportunities to take action. Your engagement—whether through contacting legislators, spreading awareness, or participating in advocacy events—can make a real difference. Together, we can push for policies that enhance research, improve access to treatments, and support families navigating the challenges of rare diseases like Dravet syndrome. Our recent blog post details other ways you can receive accurate, nonpartisan information on topics that may directly affect you and your family.
Stay informed, take action, and be a part of the movement for change! #AdvocateforDravet
Want to know more? Just click an image to explore each policy.
Upcoming Advocacy Opportunities
Prior Advocacy Opportunities
The Epilepsy Foundation has created a toolkit with advocacy options tailored to how much time you can commit. Click on an image below to learn more!
If you are not sure where to begin and want to learn more about how to advocate for our community, check out the webinar below.
Our Partners in Advocacy

Our Legislative Advocacy Program is supported by unrestricted grants from:
