Shining Stars

Shining Star Logo

All children are special, but we believe that children with epilepsy are Shining Stars! 

This program connects youth and teens with epilepsy from across Minnesota and eastern North Dakota, and encourages them to reach for the stars. All youth ages 17 and under are invited to become a Shining Star and join us with their family for special events throughout the year.

A large group of children with epilepsy and their families, in front of a screen showing the Shining Stars logo.
Photo of two people sitting in stadium seats looking at the camera and smiling.

The Shining Stars program seeks to address the feelings of isolation and difference that can often accompany an epilepsy diagnosis, especially at a young age. We help children connect with others who are facing similar challenges and seek to empower them to embrace their differences and continually strive to meet their fullest potential.

We recognize that epilepsy affects the entire family. In addition to opportunities for children with epilepsy, the Shining Stars program offers parents a chance to connect with each other. We also publish a quarterly e-newsletter with information and resources specific to parents of children with epilepsy.

All new Shining Stars will receive:

  • Shining Star Medallion
  • Program Certificate
  • Special Event Invitations
Thriving with Epilepsy

Meet Thomas Putnam

Thomas and Anna Putnam share a bond unlike any other brother and sister. They may just be the only non-twin siblings to have an SCN8A epilepsy diagnosis in the world. This rare form of epilepsy is due to a sodium channel disorder and affects the 14-year-old Thomas and 11-year-old Anna in similar ways.

Thomas' Story
A young man with blond hair in a UofM sweater stands next to his mom, smiling. The family resemblance is apparent.

Shining Star Toolkit

Help your child be a Shining Star in their community! The Epilepsy Foundation’s free Shining Star Toolkit gives suggestions about how to raise awareness and education of epilepsy in the classroom and community. After they receive their kit, let us know how they educated others so we can recognize their hard work and send a special thank you gift!

Ways to create awareness in your local community include:

  • Create a PowerPoint presentation about your journey and share it with your class
  • Write an article about epilepsy and submit it to your local or school newspaper
  • Organize a local awareness event or fundraiser
  • Educate your friends, teachers, and neighbors using EFMN’s brochures & resources
  • Participate in the annual Rise Above Seizures Walk
  • Organize a clothing drive at your school or in your community (pick-ups available in our service area)
  • “Speak Up” and share your story in November (National Epilepsy Awareness Month)
  • Request a FREE seizure training; staff from EFMN can educate your teachers and fellow students
  • Request a classroom kit filled with information & activities for your classroom
A group of kids in brightly colored tshirts stand together hold up their index fingers to indicate "one."
An older child shows a craft to a group of younger children.

2019-2020 Winning Kid – Hannah Poshek

Hannah Poshek, 15, has never really known a life without seizures. Diagnosed with generalized epilepsy with absence seizures at 13 months old, she (and her parents) spent her early childhood dealing with unpredictable and hard to control seizures, sometimes over a hundred per day.

After a lot of time trying different medication combinations, her seizures became more controllable but she was still having breakthrough seizures. When she was 8, Hannah and her family met with an Epileptologist at the University of Minnesota Health MINCEP Epilepsy Care. They were able to make medication adjustments and diet alterations that have thankfully resulted in very limited seizure activity. Through this better seizure control, Hannah was able to become involved with more and more activities. And she keeps herself very, very busy.

Hannah loves to sing, dance, and perform at every opportunity, and is part of a local dance group. She is also a Special Olympics medalist with numerous awards in swimming and gymnastics, most recently winning three gold medals and one silver medal at the Special Olympics State Gymnastics meet in June 2019. She has been a member of the Alexandria Minnesota Wild Special Hockey team for the last eight years. Through her hockey participation, Hannah was featured in the MediKidz comic book “Playing Sports with Epilepsy” alongside Olympic hockey player, Chanda Gunn. In the summer of 2019, Hannah also had the honor of being named the Minnesota Special Hockey Athlete of the Year!

To add to the long list of accolades, we are excited to name Hannah as the 2019-2020 EFMN Winning Kid! The Winning Kid program recognizes a young person with epilepsy as a leader in the community and puts them in a position to support others.

As the Winning Kid, Hannah’s list of duties includes kicking-off the Twin Cities Metro Rise Above Seizures Walk, speaking at the Annual Shining Stars Celebration, throwing out the first pitch at a Minnesota Twins game, going on stage at the Rise Above Seizures Gala, and traveling to Washington D.C. to be in the Teens Speak Up! advocacy program and meet with her congressional representatives. The Winning Kid program empowers youth with epilepsy and gives them a platform to raise awareness and be an advocate for others.

Hannah has found a lot of great opportunities and connections through her involvement with EFMN youth programs like Shining Stars and Camp Oz, which she has attended for the last four years.

“The Shining Star events and Camp Oz have been such incredible experiences for her. She’s built some incredible relationships and has found her independence. She often has said at these, she’s just one of the kids,” says her parents Chris and Sheila. “Hannah is a true individual, and we feel that her individuality has allowed her to flourish and makes her an excellent spokeswoman for kids who battle epilepsy.”

As Hannah says herself, “Don’t let anyone or anything stop you from achieving your dreams and goals.”

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Teen Virtual Connect Group

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 or 651-368-6209. In order to ensure we can



Parent Virtual Connect 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, contact Amy Haugen



Adult Virtual Connect Group

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 or 507-287-2103. In order to ensure we can provide the best experience possible, we need

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Camps for youth with epilepsy

EFMN offers summer camp programs for youth of all abilities, with the security of trained medical staff.

Camp Programs