Cystic Fibrosis Foundation

The Cystic Fibrosis Foundation is a non-profit organization dedicated to accelerating the development of new therapies and ultimately finding a cure for cystic fibrosis. It operates by funding innovative research, driving drug discovery, and establishing comprehensive standards of care for patients nationwide. Through strategic investments and partnerships, the Foundation aims to transform the lives of individuals affected by this genetic disease.

The organization was established in 1955 by a determined group of parents seeking to save the lives of their children who were suffering from cystic fibrosis. Their collective insight highlighted the critical need for dedicated resources and a coordinated effort to combat the then-poorly understood and devastating illness, leading to the formation of a unified entity focused solely on this cause. This foundational resolve propelled the initial drive for medical progress.

The Foundation serves all individuals living with cystic fibrosis, providing resources and supporting advancements that enhance their health and longevity. Its long-term vision centers on curing the disease while ensuring that every person with CF has the opportunity to lead a full and productive life. The Foundation continues to push the boundaries of medical science, striving for a future free from cystic fibrosis.