Cystic Fibrosis Research

Cystic Fibrosis (CF) is a genetic disease that primarily affects the lungs and digestive system, causing thick mucus buildup that leads to breathing difficulties and complications. Research on CF focuses on understanding its genetic causes, improving treatments, and finding potential cures. This includes developing therapies that target the faulty gene responsible for CF, such as gene therapy and medications that help the body process mucus more effectively. Advances in research are improving the quality of life for those with CF and increasing life expectancy, making it a significant area of interest in medical science.