Imagine losing two hours of your day—every day. This is what Cystic Fibrosis does to a child that wants to play and be normal.

Jaxson does thirty minutes of vest therapy every morning and every night. Then he does nebulizer treatments afterwards for Pulmozyme and saline. He also must take enzymes before every meal. Cystic Fibrosis is such a huge part of his daily life.

At three-years-old, Jaxson is already immunocompromised with lung issues and pancreatic insufficiency due to this incurable disease. His resilience to fight this disease daily makes us fighters too! We cycle for Jaxson and everyone living with Cystic Fibrosis to find a cure!

We invite everyone that loves—or likes—to cycle and support a life saving cause. Had Jaxson been born ten years ago, his life expectancy would have been greatly reduced. Thanks to medications like Trikafta (approved for two-year-olds when Jaxson was one) and Orkambi (approved for one-year-olds when Jaxson was born), his life expectancy no longer has a number! This is greatly due to the fundraising efforts of the Cystic Fibrosis Foundation. 

Please join us on this amazing ride for all the CF fighters like Jaxson, an amazing foundation, and an even better cause for all the future generations. Please don’t hesitate to reach out to me with any questions.

Let’s ride together to cure CF!!!!!!