When our son Hudson was just 9 days old, our world was turned upside down by Cystic Fibrosis diagnosis. That day, we committed ourselves to doing everything in our power to find a cure. Since then, our reality has shifted again: we have another child on the way with a confirmed CF diagnosis.
 

Cystic fibrosis is a genetic, life-shortening disease that attacks the lungs, pancreas, and other vital organs. It makes it difficult to breathe and fight off life-threatening infections. There is currently no cure, and too many people with CF die young. We are here to change that.
 

On August 23rd, I will be running the Wausau Marathon as part of the CF Breathe Team. I am running for Hudson, for our new baby, and for every individual fighting this disease. Every person with CF faces a unique and challenging journey, and while medical progress has been made, the road ahead is still far too long. We need a cure so that both of our children, and everyone in the CF community, can live a long, healthy life.
 

Will you help us end cystic fibrosis? By donating to our marathon goal or joining our fundraising team, The Roberts Salty Siblings, you are directly funding the research and science needed to find a cure. Thank you for your support.