Feeling like no one understands is one of the most common challenges people face on the journey with epilepsy. Social isolation takes a real toll on emotional and physical well-being. That’s why so much of our work is dedicated to creating spaces where people feel seen, understood, supported, and less alone.
Whether you’re living with epilepsy, caring for someone who is, or navigating a new diagnosis, finding others who get it can make a world of difference. Through connect groups, community events, and youth programs, the Epilepsy Foundation of Minnesota brings people together to share stories, build confidence, and create lasting bonds.
There’s strength in support — and power in community.
Explore the ways you can connect below.
Find strength in shared stories and experiences. Connect virtually with others who truly understand life with epilepsy. Learn more →
Make friends, have fun, and show up just as you are. Casual, inclusive gatherings for all ages — from game nights to bowling and beyond. All events across the state are open to everyone. Learn more →
Confidence, connection, and fun — all in one place. Our camps offer safe, empowering experiences for youth with epilepsy to grow, play, and belong. Learn more →
Celebrate every milestone, together. Build lasting friendships. Shining Stars connects youth and families, recognizing youth on their journey with epilepsy and cultivating space for opportunities that foster pride and community. Learn more →


MN Epilepsy Group is having a party July 23, 2026 from 5p-7p for you and your friends to come and explore everything EEG! Come experience the different parts to an EEG: Foam In, Foam Out: First, make your hands sparkly clean with lots of foamy bubbles- just like our EEG
Join us on July 23rd for a picnic gathering for individuals, families, and friends impacted by epilepsy. The Epilepsy Foundation of Minnesota will provide the main course and bottled water. Feel free to bring a store bought food item to share. You are also welcome to bring a lawn game
Adults living with epilepsy come together to meet others, share the triumphs and challenges of living with seizures and connect with those who understand the epilepsy journey. For more information, please contact Lisa Peterson at Lisa.peterson@efmn.org or 218-624-1330.
Connect Groups gave Ary and Lynn an introduction to EFMN services, as it does for many families, but the first event they attended was the Rise Above Seizures Walk in 2011. Ary’s since become involved in a variety of youth events and joined the Shining Stars program.
Ary's Story