Cystic Fibrosis (CF) treatment focuses on managing symptoms and improving quality of life. Common approaches include airway clearance techniques, which help remove mucus from the lungs, and medications like bronchodilators to open airways. Patients may also take pancreatic enzymes to aid digestion, as CF can affect the pancreas. In addition to medications, regular exercise and a high-calorie diet are recommended to maintain overall health. Newer therapies, such as CFTR modulators, target the underlying genetic defect in CF, offering hope for improved lung function and reduced symptoms. Regular check-ups with a pulmonologist are essential for ongoing care.