We envision a world where no one journeys through epilepsy alone. You can join us. Of the 55,000+ Minnesotans living with epilepsy, only two-thirds have control of their seizures. Access to quality care, food and housing security, and a supportive community are critical to living a safe, connected, and empowered
The Epilepsy Foundation of Minnesota is hosting the Torchbearer Honors on November 18, 2021, to recognize individuals across the state who have made a tremendous difference for the epilepsy community. We will be honoring individuals who have been nominated by their peers and have made an impact in our community.
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, contact Martin Hernandez
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, contact Lisa Peterson at lisa.peterson@efmn.org or 218-624-1330. In order to ensure we can provide the best experience possible, we need
This space is for teens with epilepsy to meet others who understand the journey they’re on. Join us to hang out, make new friends, and talk about growing up and living with epilepsy. For more information, contact Angela Bowles Edwards at abedwards@efmn.org or 651-368-6209. In order to ensure we can
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, contact Amy Haugen
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, contact Martin Hernandez at mhernandez@efmn.org or 507-287-2103. In order to ensure we can provide the best experience possible, we need
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 Angela Bowles Edwards at abedwards@efmn.org or 651-368-6209.
This space is for teens with epilepsy to meet others who understand the journey they’re on. Join us to hang out, make new friends, and talk about growing up and living with epilepsy. For more information, contact us at rsvp@efmn.org. In order to ensure we can provide the best experience
A space for people impacted by a rare epilepsy or complex diagnosis to meet others and talk about life updates, challenges, and successes with others who understand the rare epilepsy/complex diagnosis journey. This includes parents and caregivers to children with rare epilepsy, as well as adults. This is a group