At just seven weeks old, Cooper was diagnosed with Cystic Fibrosis (CF), a genetic disorder that turned our world upside down. We'd never heard of it before, but quickly learned CF is a life-shortening disease that severely damages the lungs, pancreas, and other vital organs. Cooper's journey began at the CF Clinic at Children's Health in Dallas, where we learned his inability to absorb nutrients, placing him in the less than 1st percentile for weight, was due to CF. The nightly cough that worried us was caused by mucus buildup in his lungs, a constant struggle for those with CF, making breathing a constant challenge and leaving them vulnerable to life-threatening infections.

Today, Cooper is thriving. He's reached the 40th percentile for weight, thanks to enzyme supplements along with twice-daily breathing treatments to clear his lungs. He's a joyful toddler, fascinated by the world around him, and loves Bluey, books, and playing with his older sister. While he's made remarkable progress, the fight against CF is far from over. We're joining the Great Strides event this year to help support their mission to fund research, treatments, and ultimately, a cure for cystic fibrosis once and for all. Any and all contributions are greatly appreciated!