All 2019 Proceeds to Benefit Clayton Epps

August 10th, 2019
Memorial Park
300 S. Main St.
Payson, Utah 84651

5k & 1 mile: 8:30am

Breakfast: 8:30am-10:00am

Activities for the whole family: 8:30am-12:30pm

Taco Truck: 11:00am-12:30pm 

Register Today

Team Carter 5k & 1mile family fun walk

Bikes, scooters and strollers welcome for the kids!

Pancake breakfast to follow

Medals for the first 50 kids



2019 proceeds will benefit Clayton Epps

Meet Clayton!

 

 Clayton is 2 years old and is often called by his family “Baby Cinco” because he’s the youngest of 5 children. He lives in Payson, Utah with his parents Jim and Bethany, his brothers Braddock (12) and Dawson (8), and his sisters Emmalee (11) and Annabelle (4). He also has the blessing of having his “Nanna” (aka grandma) live with him. She could easily be considered Clayton’s hero because she is ALWAYS there for him. Clayton is extremely lovable and is adored by those who know him. He loves Winnie the Pooh and has recently become fascinated with all things spiders and Spiderman. You can often find him dancing to a good beat or wrestling on the floor with his big brothers. He loves books, cars, and playing outside in the sandbox. 

In April of 2019, Clayton was diagnosed with Optic Nerve Glioma, a large grape-sized malignant tumor growing on the optic nerve of his right eye. He began chemotherapy treatments a week after diagnosis and will continue them for at least the next year, depending on the tumor’s aggression.  Because of the chemo therapy, Clayton’s immune system is compromised, which means he has to be very careful with germs. Despite having to be hospitalized for infection previously, Clayton’s disposition has been one of constant happiness! He teaches his family every single day to have faith and find joy amidst the misfortunes that have taken place. Though he’s just a little guy, he has been resilient in the fight to push forward! We have also witnessed “mountains move” for Clayton because of the faith and loving outreach from others, which is why we set up a Facebook page for him called “Moving Mountains for Clayton”. Clayton’s diagnosis, although heartbreaking, has helped bring our family closer together and has reminded us of what really matters. We are grateful for our tender-hearted, bright-eyed little boy and the blessing that he is to us in our home and in the community. 

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