The Epilepsy Foundation of Minnesota Blog

We woke up this morning at Camp Oz still riding high on the joyful feelings from the impromptu dance party in the A-Field last night after Predator vs Prey. There was music. There was a 25 person long Can-Can line. There were multiple cha-cha lines. There was singing. There were

Campers were in their groove today as they got an extra hour of sleep to prepare for a full day of wild activities!   The dining hall was wafting wonderful smells this morning as campers entered the dining hall ready to wolf down some waffles with maple syrup and lil’ smokies! 

The second full day of camp is in the books and who could have thought that temperatures in the high 80’s would feel so pleasant and comfortable! Breakfast was moved back an hour later to allow for more sleep and recharging for the day ahead and our campers took full

The first full day of Camp was hot, hot, hot but that didn’t stop our campers from diving head first into some great activities. Each cabin group was scheduled for two main activities in the morning and then two again in the afternoon with plenty of cabin bonding time spread

Today marked the first day of in person Camp Oz in over 2 years and it is off to a great start! It was a hot one today, but over 60 campers and their families checked in today to have a week full of adventure and fun! Campers met their cabinmates

What have we learned about COVID and epilepsy and its effects on seizures among adults and children? An update with two years of information.

“I was so excited to be at Camp Oz because it was the first time I had ever stayed away from my parents. I wanted to go to Camp Oz because I wanted to make new friends and I love to be independent,” says Shreya.

The Epilepsy Foundation of Minnesota’s (EFMN) promise is that nobody journeys through epilepsy alone. Marcia Kautz’s journey shows just how important this statement is. Marcia and her husband Dean have been journeying together since her first seizure in 1988, and the partnerships they’ve built along the way have been life-changing.

The Necastro family’s epilepsy journey began in 2019 when Noah was eight years old. They immediately learned of our programs and events from their neurologist, and it quickly became a journey filled with support and education. The support came from joining family programs like the annual Walk, Parent Connect Groups,

What have we learned about COVID and epilepsy and its effects on seizures among adults and children? An update with two years of information.