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, or if you have questions, please contact Lisa Peterson at lisa.peterson@efmn.org or 218-624-1330. To
Join with others in your district to learn how legislative candidates stand on policies that impact Minnesotans with brain injury and other disabilities. All sessions take place from 6:30 to 7:30 p.m. via Zoom. Please use this link to register for the Town Hall Forum in your Minnesota Senate District.
Parents 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 Angela Bowles Edwards at abedwards@efmn.org or 651.368.6209. In order to ensure we can provide the best experience possible,
Join with others in your district to learn how legislative candidates stand on policies that impact Minnesotans with brain injury and other disabilities. All sessions take place from 5 to 6 p.m. via Zoom. Please use this link to register for the Town Hall Forum in your Minnesota Senate District.
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
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 Angela
Join us for a live, acoustic afternoon show with contemporary Christian music singer/songwriter Jason Gray. Doors open at 2:30. There will be no donation requests made during the concert. Buy tickets. DIY fundraiser hosted by Carrie Buck and Chuck Semrow.
La epilepsia puede ser una condición aislante sin el apoyo de otros, pero creemos que nadie deberÃa tener que enfrentar la epilepsia solo. Esta reunión virtual es una oportunidad para conectarse con otras personas hispanohablantes, compartir experiencias y dar/recibir apoyo. Están bienvenidos personas con epilepsia, cuidadores, padres, o otros seres
Join us for a non-partisan Rev UP MN Virtual Candidate Forum for Senate District 56 featuring candidates for the Minnesota Senate and House Districts 56A & 56B. Register here. Don't know what district you are in? Find out here.
Sudden Unexpected Death in Epilepsy (SUDEP) is a difficult topic to discuss, both for those living with epilepsy and the doctors who treat them. In this webinar, Alison Kukla and Cate Brocker from the Epilepsy Foundation of America will cover what is currently known about SUDEP, how to approach this