My CF Climb Story

We welcomed our beautiful daughter, Quinn, into the world 4 months ago. When she was just shy of 2 weeks, she was diagnosed with Cystic Fibrosis and our world changed forever.

It has been a very difficult road thus far, but we are blessed and grateful to have the best village of friends, family and the best CF team in the world.

We are participating in our first CF foundation fundraising event, The Climb, at Lincoln Financial Field on November 9, 2024.

Please consider donating to our team, not just for Quinn, but to help find the cure for everyone with Cystic Fibrosis.

Nearly 40,000 people in the United States have cystic fibrosis: a progressive, genetic disease that affects the lungs, pancreas, and other organs. They are moms, dads, sisters, brothers, daughters, sons, and friends who face the sobering prospect of a shortened lifespan. I climb for them.

Working alongside the CF community, the CF Foundation has fostered the development of more than a dozen CF treatments and helped add decades of life for people with CF. Yet, many people with CF do not benefit from existing therapies. Our vision is a cure for every person with cystic fibrosis – a life free from the burden of this disease – and we will not leave anyone behind.

Please support me!
By supporting my fundraising goal, you have an opportunity in your lifetime to be part of ending this disease. Please consider joining us and help make medical history.