Cystic Fibrosis Foundation's Board Chair KC White Sheds Light on Disease and Progress in Care

The Cystic Fibrosis Foundation's Board Chair, KC White, recently participated in a media tour to shed light on the disease, her personal journey, and the Foundation's efforts to advance care and treatment options. CF is a rare, genetic disease impacting people of all races and ethnicities, with about 40,000 cases in the U.S. KC White, the first person with CF to serve as board chair, shared her inspiring story and discussed recent treatments known as modulators that have transformed the health of about 90% of the CF population. The Foundation is committed to finding a cure and providing long, fulfilling lives for all people with CF through funding research, advancing care, and supporting the CF community.