There’s still no cure for cystic fibrosis, and far too many people with CF die far too young. As the mom of two boys living with CF, this reality hits home every single day. That’s why I’m walking this year—to help change that.
 

Cystic fibrosis is a genetic, life-shortening disease that affects the lungs, pancreas, and other vital organs. It makes breathing a constant struggle and fighting off life-threatening infections even harder. For my boys, it means daily treatments, medications, and potential hospital visits—just to stay healthy enough to keep living.
 

But despite the challenges, the research and advancements brought about by the Cystic Fibrosis Foundation have made a world of difference in their lives. They’ve given my boys a chance to dream, to grow, and to live a life that, not long ago, wouldn’t have seemed possible.
 

CF is different for every person who has it. Each journey is unique, and while we’ve made incredible progress, the road ahead is still long. Too many people with CF are still fighting to survive, and too many families are losing loved ones far too soon. That’s why we need a cure—a cure that will give every person with CF a real chance at a long, healthy life.
 

Will you help us make that happen?

By donating to my fundraising goal, you’re not just supporting my family—you’re helping fund the research and science that will bring us closer to a cure for everyone living with cystic fibrosis. Together, we can change the future.
 

Thank you from the bottom of my heart. 💙