Â
Cystic Fibrosis (CF) is an inherited chronic disease that affects the lungs and digestive system of about 30,000 children and adults in the United States (70,000 worldwide). Â A defective gene and its protein product cause the body to produce unusually thick, sticky mucus that clogs the lungs and leads to life-threatening lung infections and obstructs the pancreas and stops natural enzymes from helping the body break down and absorb food.
Â
In the 1950s, few children with cystic fibrosis lived to attend elementary school. Â Today, advances in research and medical treatments have further enhanced and extended life for children and adults with CF. Â Many people with the disease can now expect to live into their 40s and beyond.
Â
Since 1955, the Cystic Fibrosis Foundation has been the driving force behind the pursuit of a cure for CF.  Thanks to the dedication and financial backing of our supporters – patients, families and friends, clinicians, researchers, volunteers, individual donors, corporations and staff, we are making a difference.