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+.
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.
On June 25-27, 2021, we will combine our camps into Camp Never Give Up! and provide virtual and in-person programming for youth with epilepsy ages 8-17. Virtual programming will be held on June 25 & 27, and we will offer a safe, socially distanced in-person experience on June 26 in Evergreen, Colorado Springs and Ft. Collins.
Camp Never Give Up!
June 25-27, 2021
Online and at a park near you
Thank you to our 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 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 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.
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