We’re empowering Minnesotans impacted by epilepsy through support, education, connection, and advocacy so no one faces epilepsy alone.
Donate your gently used clothing to support epilepsy programs across Minnesota. Our curbside pick-up service is free, easy, and impactful, turning your donations into vital support for our local programs.
Schedule a pickup →
Specialized Outreach Managers are here to provide free, personalized support—whether you have a quick question or need ongoing help.
Explore our support options →
There are many ways to make a difference—whether you give monthly, support an event, make a one-time gift, or a leadership gift. However you choose to give, you’re helping drive innovation, expand critical programs, and transform what’s possible for the epilepsy community in Minnesota.
Make a gift →



Explore real stories, breakthroughs, and hope for the epilepsy community.
In May 2026, the Epilepsy Foundation of Minnesota (EFMN) welcomed 50 individuals and families impacted by epilepsy to Thumper Pond Indoor Waterpark in Ottertail for a day filled with splashing, laughter, connection, and community.
In May 2026, EFMN hosted its inaugural EpiForum, bringing together clinicians, researchers, healthcare leaders, and industry partners for an evening focused on Emerging Technologies in Epilepsy Care.
Anyone impacted by epilepsy is welcome to join Babs for coffee and conversation at her monthly opportunity to connect. If you enjoy a creative activity such as writing or crafting, you’re welcome to bring your project with. RSVPs are encouraged but not required. Please contact Babs Larson to RSVP or
Join EFMN in Duluth at the Lester Park Pavilion for a potluck picnic on Thursday, June 18th for a gathering of community members impacted by epilepsy. The Epilepsy Foundation of Minnesota will provide the main course and bottled water. You’re welcome to bring a store bought food item to share.
Meet other parents, grandparents, and caregivers who live day-to-day caring for a child with seizures and/or epilepsy. This is an opportunity to meet others, offer peer-to-peer support, share resources and experiences, and talk honestly about the triumphs and challenges of a child’s epilepsy journey. For more information, please contact Lisa