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 →


Join other parents/caregivers of a nonverbal child with epilepsy for a space to share your experiences and support and encourage one another. This group meets quarterly over Zoom, and it is led by EFMN volunteers Joel Virtue and Carissa Burns. To RSVP or ask questions, you can reach Joel by
Moms of adult children with epilepsy are invited to attend this support group where moms of adult children come together and share their journey and experiences. We support each by providing a safe space for everyone to express how they are feeling and share about the challenges and joys of
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, Chris Merrill
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