Idiopathic Pulmonary Fibrosis (ipf)
Idiopathic pulmonary fibrosis (IPF) is a rare and progressive lung disease characterized by scarring or thickening of the lungs. IPF makes it increasingly difficult for the person to breathe over time and is considered a terminal diagnosis. Symptoms of IPF include shortness of breath, coughing, fatigue, chest tightness, and inability to exercise. Unfortunately, there is no cure for IPF, but medications and treatments can help to slow the progression of the disease. Early diagnosis and treatment is crucial in managing IPF and improving its prognosis.
← International Journal of Thorax