Cystic Fibrosis is a genetic disorder that primarily affects the lungs and digestive system. It is caused by mutations in the CFTR gene, leading to the production of thick, sticky mucus that can clog airways and trap bacteria, resulting in frequent lung infections. Individuals with Cystic Fibrosis may experience symptoms such as persistent cough, difficulty breathing, and poor growth. While there is no cure, treatments are available to manage symptoms and improve quality of life, including medications, physical therapy, and nutritional support.