Where Empowered Journeys Begin

The Epilepsy Foundation is a national nonprofit dedicated to improving the lives of people affected by epilepsy. For more than 50 years, the Foundation has promoted epilepsy awareness, funded research, advocated for laws, and helped to improve access to care for the epilepsy community. We are the first stop for many people who receive an epilepsy diagnosis or have a question along the way. Through education, advocacy, research, and connection, the Foundation is where empowered journeys begin.  

Where You Belong

The Epilepsy Foundation is here to guide people through managing their health and well-being, at any stage in their epilepsy journey. A trusted resource for education and support, we help individuals and families navigate the complexities of epilepsy and make informed decisions. Our Editorial Board of renowned medical experts ensures content is relevant and accurate, ultimately helping people understand epilepsy and manage their seizures.  

Stronger Together

Community is at the core of our work to create an environment where people can find support, connect with others, and share experiences. Our network of local partners offer support and resources and amplify the voices of people in their communities. The epilepsy community comes together at in-person and virtual events through:

• Social media
• Personal stories
• Volunteer opportunities
• Support groups

We find strength in numbers to navigate the epilepsy journey for individuals and families, parents and caregivers, and friends and allies, so no one faces epilepsy alone.

Insight to Impact

The Foundation is dedicated to sharing the latest developments in epilepsy research and education. We support research initiatives that lead to better treatments and care, and offer training and educational programs, including seizure first aid. Innovative programs help improve communication between people with epilepsy, their families, advocates, researchers, and investors. Sharing knowledge empowers everyone, across communities and demographics, toward better health equity. Our newest program empowER&D, “Empowering Epilepsy Research & Development,” reimagines epilepsy research and development through strategic collaborations and patient-centered innovation.  

Agents of Change

We empower individuals with epilepsy to become their own advocates, champion better epilepsy care, and combat stigma. Our priorities include ensuring access to quality healthcare, protecting the rights of people with disabilities, and promoting education about epilepsy. Epilepsy advocates help raise awareness and educate decision makers to move the Foundation’s priorities forward. Whether you’re living with epilepsy or supporting a loved one, your voice and experience have the power to shape a future where no one faces epilepsy alone.