Understanding Cystic Fibrosis and Local Support
Cystic Fibrosis (CF) is a genetic condition that causes persistent lung infections and breathing difficulties. The lungs contain large airways called bronchi and smaller ones called bronchioles. Normally, these airways are lined with thin mucus layers that trap dust and germs, while tiny hair-like cilia move the mucus out of the lungs.
For individuals with CF, the mucus becomes thick and sticky, making it difficult for cilia to clear germs. This buildup can lead to chronic coughing, frequent infections, and progressive lung damage. Although there is no cure, early intervention and access to specialized care can control infections and slow disease progression.
The Cystic Fibrosis Foundation Rocky Mountain Chapter serves as a vital resource for families navigating these challenges.