Its hard to believe Austin is going to be 3 already in a couple weeks. He is at that age where we have so much fun being with him. When we are chasing him around a park its easy to forget that he has Cystic Fibrosis. He is as active and rambunctious as any kid his age. It is only thru the work of the Cystic Fibrosis Foundation that have allowed children like Austin to live normal lives. While they have made tremendous strides in treating the symptoms, there is still no cure. That is why we are committed to helping find a cure for cystic fibrosis and why we are raising funds to support the Cystic Fibrosis Foundation. Contributions to our personal fundraising page go to the Annual Fund which provide important, unrestricted resources that help develop new treatments and pursue every opportunity for promising research that can lead to a cure. Please consider making a gift today. Your support will help make a difference for all those with CF and their families. Thank you!