Cystic fibrosis is a hereditary condition that causes damage to the digestive system, lungs and other parts of the human body. It commonly affects the cell that produces sweat, digestive juices, and mucus. Though currently, it has no cure, the conditions can be controlled to prevent complication and improved the patient quality of life. Specialists in cystic fibrosis will prepare a comprehensive treatment plan for the patient. Medications commonly used include antibiotics, the medications that make mucus thinner, ivacaftor, bronchodilators, and steroids. The patient is also taught maneuvers on how to deal with the condition.