Get Connected

Belonging isn’t a luxury — it’s a core part of well-being.

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.

Connect Groups

Find strength in shared stories and experiences. Connect virtually with others who truly understand life with epilepsy. Learn more  

Social Events

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  

Camp Programs

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  

Shining Stars

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  

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16

Apr

Parent/Caregiver Connect

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 Erik

21

Apr

Spanish Connect Group

La epilepsia puede ser una condición aislante sin el apoyo de otros, pero creemos que nadie debería tener que enfrentar la epilepsia solo. Esta reunión virtual es una oportunidad para conectarse con otras personas hispanohablantes, compartir experiencias y dar/recibir apoyo. Son bienvenidos personas con epilepsia, cuidadores, padres, u otros seres

22

Apr

2026 Day at the Capitol

This annual afternoon of advocacy will bring together individuals with epilepsy, caregivers, loved ones, and supporters of the epilepsy community for meaningful engagement at the Capitol. Participants will gather to connect with Minnesota legislators, share personal stories, and advocate for policies that support the wellbeing of Minnesotans impacted by epilepsy.

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Thriving with Epilepsy

Meet Ary Rodeghiero

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
Mom holding hands with 10 year old daughter at theme park

Register by April 25 to Save on EFMN Summer Camps!

 Camp Oz, Day Camp, and Family Camp offer safe, fun summer experiences for youth with epilepsy (ages 5–17) and their siblings.