When I was pregnant, we learned that our son, Atlas, would be born with cystic fibrosis. It was devastating news—especially after believing we might never have a child at all. In that moment, everything felt uncertain and overwhelming.

We were told by genetic counselors that we had the option to “start over.” But for us, that was never a choice. Atlas was already our son, and we were determined to learn everything we could and do everything in our power to give him the best life possible.

We are incredibly grateful for our clinic, who supported us even before Atlas was born. They gave us not only information, but something we desperately needed—hope.

Since then, Atlas has faced his share of ups and downs with his health. But through it all, he remains unbelievably strong, full of joy, and resilient in ways that inspire us every single day. He is truly our hero.

Cystic fibrosis is a genetic, life-shortening disease that affects the lungs, pancreas, and other vital organs. It makes it difficult to breathe and to fight off serious infections, often leading to long-term lung damage and respiratory failure. While treatments have improved, there is still no cure—and too many lives are cut far too short.

Every person with CF has a different journey, but they all share one thing: the need for better treatments and, ultimately, a cure.

That’s why we’re walking—to be part of the change.

Will you join us?

By donating to our fundraiser, you are helping support critical research and advancements in care. You are helping bring hope to families like ours. And most importantly, you are helping move us closer to a cure for everyone living with cystic fibrosis.

Thank you for supporting Atlas and for being part of this fight with us.