When our children were given the diagnosis of cystic fibrosis, all we had was devastating statistics and hope. We always have hope! Our hope has given way to confidence and our confidence to the expectation that one day a cure will be found. It’s not if but when. 

 

Following the final Breath of Hope in 2024, my family and I committed to a year of national CF Foundation events. We want to take time to listen and learn in the CF community about the great needs that remain today.

 

Together, let’s write the last chapter of CF.