Cystic Fibrosis

Cystic Fibrosis (CF) is an inherited and potentially life-threatening condition which affects the lungs, digestive system and other organs in the body. It is caused by a genetic mutation in the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) protein. People with CF have an abnormally thick and sticky mucus which builds up and can cause severe respiratory and digestive problems. Without treatment, CF can lead to complications such as chronic lung infections, poor nutrition and, in some cases, death. CF is the most common genetic disorder in the world and affects an estimated 70,000 people. The good news is that there is hope for those affected by the condition. With early diagnosis and proper treatment, people with CF can live longer and healthier lives. In recent years, improved treatments and greater understanding of the condition have led to a dramatic increase in life expectancy for those living with CF. The future of CF treatment is focused on finding a cure for the condition, as well as treatments that can reduce symptoms and improve quality of life.