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.
Join other partners for an hour to discuss the highs and lows of your journey and hear from other significant others about how we best care for ourselves while caring for our loved ones with epilepsy. For questions or to RSVP, contact James Schaefer at james.schaefer84@gmail.com or 612.280.9643 or JP
Adults parenting while living with epilepsy are invited to come together to meet others, share the triumphs and challenges of living with seizures and connect with those who understand the epilepsy journey. Significant others and children of the adult with epilepsy are welcome to join the meeting with their person.
Join other parents/caregivers of a nonverbal child with epilepsy for a space to share your experiences and support and encourage one another. This meets quarterly over Zoom, and it is led by EFMN volunteer, Joel Virtue and Kim Olson. To RSVP or ask questions, you can reach Joel by email
We offer a wide variety of programs and services for youth and adults across our service region.
As someone living with epilepsy, I know firsthand how challenging it can be to navigate not only the medical side of things, but also the social and financial barriers that come with it. But I also know how powerful advocacy can be—not just for yourself, but for an entire community.
The Epilepsy Foundation of Minnesota (EFMN) has a long and rich history of advocacy. From our early efforts to raise awareness to our impactful policy successes—reducing license suspension time after a seizure, enacting Step Therapy Reform, passing Seizure Smart Schools legislation, and most recently, securing coverage for Seizure Detection Devices
Your gift helps us educate, connect, and empower those with epilepsy and their families.