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 →
Adults 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. This group gathers in the meeting room at FM Area Foundation. If you have questions, please contact Outreach Manager Lisa
A space for young adults with epilepsy to meet others and talk about life updates, challenges, and successes with others who understand the epilepsy journey. This is a young adult-led group looking to create peer-to-peer support and connection. For more information, please contact Lisa Peterson at Lisa.peterson@efmn.org or 218-624-1330.
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, contact James Schaefer at james.schaefer84@gmail.com or 612.280.9643, JP Yorro at jpyorro@gmail.com or
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 StoryJoin us for the United in Epilepsy Regional Walks!