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The Epilepsy Foundation of Minnesota periodically features a “Thriving with Epilepsy” story about everyday heroes living with epilepsy in our community.
Seizures can strike at any moment. Imagine living your everyday life seizure-free, and then one day you are faced with a life-altering diagnosis. After receiving news that their daughter Jacqui was diagnosed with epilepsy at age 14, the Mattison family learned to cope with her seizures and find support through EFMN.Read More
Misty and JP Rennquist’s daughter, Julia, was diagnosed with epilepsy three years ago. Although fully aware of her seizures, Julia is a rambunctious, funny and very sweet five-year-old. The Rennquist family found support through EFMN early on and celebrates Julia’s epilepsy journey every year at the Rise Above Seizures Walk.Read More
Steve has given generously to EFMN to ensure that kids with epilepsy experience the fun and friendships of a week at Camp Oz. Although Camp Oz was not available when Steve was diagnosed with epilepsy as a child, he now visits every year to experience the contagious joy of the campers.Read More
This month, we would like to introduce you to one of our families from North Dakota. Meet Griffin Walker, a 14-year-old teenager living with epilepsy. He is a two-year veteran of EFMN’s Camp Oz program, a Shining Star member and strives to be his best while rising above seizures every day. Hear from his mother, Roxann, as she shares her son’s journey and the positive impact EFMN has made on Griffin’s life.Read More
We are pleased to introduce you to Hafsa Yusuf, a Winona State University freshman, an Elam Baer & Janis Clay Scholarship recipient, and Day Camp volunteer.Read More
Meet Taylor Johnson: a recent Hamline University graduate, a former participant in EFMN’s Shining Star program, a dedicated epilepsy advocate, and one of Epilepsy Foundation of Minnesota’s newest board members.Read More