The Cystic Fibrosis Awareness Foundation is a non-profit 501(c) (3) dedicated to raising money to help fund research for treatments and cure. The foundation has recently increased its outreach in order to help families that are impacted by the disease.
Our daughter Caitlin born in 1995 and has graduated from college. She was diagnosed with Cystic Fibrosis at 3 months old. Caitlin also has a brother, Tim who is 20 years and does not have CF. CF is a battle and is filled with ups and downs. Caitlin is an active young adult and is doing well.
Cystic Fibrosis is a rare chronic inherited life-threatening disorder that affects the lungs and digestive system. There is no cure. To learn more about the disease check out the Cystic Fibrosis Foundation
Non-profit Foundation for Cystic fibrosis