This year I’m fundraising for the Cystic Fibrosis Foundation in honor of my sweet son, Lane, who was diagnosed with cystic fibrosis in August. Lane may only be a baby, but he’s already shown us so much strength, joy, and resilience.

Cystic fibrosis is a rare genetic disease that affects the lungs, digestive system, and other parts of the body. Right now, there is no cure—but research and new treatments are giving kids like Lane the chance to live longer, healthier lives.

Our family is walking and fundraising to help make CF stand for Cure Found. Every dollar brings us closer to breakthroughs that will change Lane’s future and the future of everyone living with CF.

If you’re able, we’d be so grateful for your support—whether that’s through a donation, joining our team, or simply sharing our story. Together, we can give Lane and others with CF a brighter tomorrow. 💙