About Us

Our son Carson was diagnosed with Cystic Fibrosis at only 11 days old.  Not knowing anything about the disease, we have since learned Cystic Fibrosis (CF) is a chronic, genetic disorder which has devastating effects on the lungs and digestive system.  About 30k Americans have CF and about 10 million are symptomless carriers (many like us who didn't even realize it).

While this is a very serious disease, we feel with continued awareness, education and research, a cure will be found for Carson and all others affected.  Carson's Crew was established by our family and friends to help in our mission of raising funds for the Cystic Fibrosis Foundation (CFF).  With no federal support, the foundation is the primary vehicle for funding CF research.  Currently, over 30 promising drugs are in the treatment pipeline (including a few which are aiming to address the root cause of the disease).

Thanks for taking the time to read about us and for your support!

Shaun, Alison & Carson