IPF, or idiopathic pulmonary fibrosis, is a serious and progressive lung disease. It is a chronic and irreversible condition in which the lung tissue becomes thickened, stiff, and scarred over time, which can make it difficult for the lungs to function properly.
IPF is a life-threatening condition with a poor prognosis. The average life expectancy after diagnosis is typically between three to five years, although some people may live longer. There is no cure for IPF, and treatment options are limited, so it’s important to seek medical attention as soon as possible if you suspect you may have this condition.
