Kid's Corner

There are nearly 8,000 kids in Colorado who have epilepsy. That means, if you have epilepsy, you are not alone. It’s not always easy to live with this condition, but connecting with other kids who know what you’re going through can help.

We offer a variety of programs to get involved with, including summer camp, youth council, Kids’ Crew, and a support group just for teens 13+. 

Summer Camp

Epilepsy Foundation of Colorado Summer Camps provide opportunities for children and teens whose lives are impacted by epilepsy to build confidence, make new friends, and have fun. Our summer camps fuel kids with the knowledge that they are not alone on their epilepsy journey. Connecting with other campers fosters resiliency, joy, and a sense of belonging. 

“I’m one of the pediatric epilepsy doctors at Children’s Hospital of Colorado and was asked to speak to the patients in an Ask the Doctor session at camp. It was a great experience answering the kids and teens questions which ranged from driving to whether they could skydive or scuba in the future. It was also wonderful meeting the kids in a non-threatening environment where they could truly feel free to ask their doctor a question on the meaning of epilepsy to them and not to their parents’ concerns. It brought me back to why I went into medicine in the first place; to make a lasting effect on a patient’s life and to provide education and comfort to others.”

– Susan Koh, MD, Associate Chief of Clinical Services, Child Neurology, Children’s Hospital 

Stay Tuned for 2022 Dates!

Contact Marcee at marcee@epilepsycolorado.org with questions.

Thank you to our 2021 Camp Sponsors!

Youth Leadership Opportunities

Youth living with epilepsy who become involved in leadership can give back to the epilepsy community while having many wonderful opportunities.  Kids who participate in our leadership programs develop important life skills, gain confidence, become a leader and engage with others who are living with epilepsy.

Youth Council

Youth Council is for teens/young adults ages 14-22 who have been diagnosed with epilepsy or are a sibling or a child of a parent who has been diagnosed with epilepsy. If you are compelled to make a difference and speak out about epilepsy, this could be the opportunity for you! 

Kids Crew

Kids Crew is for youth under 14 years old who are affected by epilepsy.  If you are a natural born leader and want to speak out about epilepsy, this may be the opportunity for you. 

Learn how to get involved.

Teens Speak Up!

Teens Speak Up! is one of our centerpiece advocacy initiatives. Every year, one accomplished teen and their parent or caregiver is selected to join over 150 other advocates from around the nation, including Epilepsy Foundation staff, parents, teens, doctors, and volunteers, in Washington DC to speak with Congress and share their stories of living with epilepsy.

Teens Speak Up! provides an opportunity for teens with epilepsy and their parents to visit the nation’s capital, receive advocacy training, meet with their legislators, and tell their personal stories. 

Teens are nominated by Foundation staff and selected by the National Epilepsy Foundation to participate in the program. After receiving training at TSU, each teen turns that training into action back here in Colorado through the Year of Service program.  If your teen is interested in learning more, please contact us!  Information about recent TSU events can be found here