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.
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Specialized Outreach Managers are here to provide free, personalized support—whether you have a quick question or need ongoing help.
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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.
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Explore real stories, breakthroughs, and hope for the epilepsy community.
In April, the Epilepsy Foundation of Minnesota returned to the Minnesota State Capitol for our first in-person Day at the Capitol since 2019. Advocates from across the state joined EFMN staff and volunteers to share their experiences with legislators, helping deepen understanding of how epilepsy and seizures shape daily life for Minnesotans.
Explore highlights from the 2026 Epilepsy Leadership Conference, where EFMN joined national leaders to strengthen connections, share insights, and collaborate.
Adults impacted by epilepsy are welcome to attend this monthly peer-led in-person group to meet others who can relate to their experiences of managing epilepsy. The group will meet at an open table, and guests are welcome to order their own food/beverage. Find them on Facebook: https://www.facebook.com/groups/1575034473435235 Facilitator: Desiree Gregorich: pugtekk@gmail.com, 218-310-4885
“Anyone personally impacted by epilepsy or interested in learning more about epilepsy is welcome to join us for a monthly opportunity to connect with others who can relate to your experiences. The meetings start with a light dinner followed by a time of connecting while enjoying activties such as playing
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 Erik