Interstitial Pulmonary Fibrosis

Interstitial pulmonary fibrosis (IPF) is a serious lung disease that causes scarring (fibrosis) of lung tissue, making it harder for the lungs to function properly. This thickening and stiffening of lung tissue can lead to difficulty in breathing and reduced oxygen intake. Symptoms often include a persistent dry cough and shortness of breath, especially during exertion. The exact cause of IPF is often unknown, but it can be associated with environmental factors, smoking, and certain medical conditions. While there is no cure, treatments can help manage symptoms and improve quality of life.