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Our Guiding Philosophy:

Educate

Seizure trainings for your school, workplace, and community at no cost.

Connect

No one should face epilepsy alone; meet people who understand what you’re going through.

Empower

Take back control with access to the information and advice you need.

A woman in a maroon sweater leans an arm over her young son's wheelchair, listening intently to someone off camera.

Help When You Need It

No one should face epilepsy alone. Whether you’re newly diagnosed or have been living with epilepsy for years, we’re here to support you.

Upcoming Events

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03

Jun

Moms Supporting Moms of Adult Children with Epilepsy Peer Led Connect Group

Moms of adult children with epilepsy are invited to attend this support group where moms of adult children come together and share their journey and experiences. We support each by providing a safe space for everyone to express how they are feeling and share about the challenges and joys of

05

Jun

Duluth Potluck Picnic

Join EFMN in Duluth at the Lester Park Pavilion for a potluck picnic on Thursday, June 5 for a gathering of community members impacted by epilepsy. The Epilepsy Foundation of Minnesota will provide the main course and bottled water.  You’re welcome to bring a store bought food item to share.

05

Jun

Partners of Someone with Epilepsy Peer Led Connect Group

Join other partners for an hour to discuss the highs and lows of your journey and hear from other significant others about how we best care for ourselves while caring for our loved ones with epilepsy. For questions or to RSVP, contact James Schaefer at james.schaefer84@gmail.com or 612.280.9643 ,  JP Yorro at jpyorro@gmail.com or

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Dive in Deeper

We offer a wide variety of programs and services for youth and adults across our service region.

Thriving with Epilepsy

Statement from the Executive Director of the Epilepsy Foundation of Minnesota on HHS and CDC Reductions in Staff 

Dear community,  The Department of Health and Human Services (HHS) recently announced cuts that have eliminated the Centers for Disease Control’s (CDC) Epilepsy Program staff. This comes as part of a large-scale Reduction in Workforce, not only at the CDC, but also other HHS agencies like the National Institute of

Empowering Change: Kyah’s Journey with Epilepsy and the Power of Advocacy

As someone living with epilepsy, I know firsthand how challenging it can be to navigate not only the medical side of things, but also the social and financial barriers that come with it. But I also know how powerful advocacy can be—not just for yourself, but for an entire community.

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Ways You Can Help

Your gift helps us educate, connect, and empower those with epilepsy and their families.