Seizure trainings for your school, workplace, and community at no cost.
No one should face epilepsy alone; meet people who understand what you’re going through.
Take back control with access to the information and advice you need.
No one should face epilepsy alone. Whether you’re newly diagnosed or have been living with epilepsy for years, we’re here to support you.
A place for people to share their experiences, their encouragement and support for one another and to network together. Supporting each other goes beyond just sending an encouraging message, which we do rely on through difficult stages in our journey and we allow this space for each other to steam
Stop by the Brainerd Caribou @ 425 8th Ave NE to connect with Lisa Peterson and others impacted by epilepsy.
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
We offer a wide variety of programs and services for youth and adults across our service region.
BLOOMINGTON, MN — July 15, 2024 The Epilepsy Foundation of Minnesota (EFMN) is thrilled to announce Jenna Carter as its new Executive Director. Carter’s dynamic leadership marks a new chapter for EFMN, which celebrates its 70th anniversary this year. With a renewed focus on equity and a commitment to its
The Epilepsy Foundation of Minnesota (EFMN) is excited to introduce the newest Outreach Manager, Nohely Arteaga! Nohely is a certified Community Health Worker, Certified Health Unit Coordinator and pursuing a Bachelor’s in Public Health at St. Katherine’s University. As Outreach Manager for Latino Communities, Nohely will be the primary contact
Your gift helps us educate, connect, and empower those with epilepsy and their families.