Idiopathic Pulmonary Fibrosis (IPF)

Idiopathic Pulmonary Fibrosis (IPF) is a chronic lung disease where the tissue around the air sacs (alveoli) becomes thickened and scarred over time without a known cause. This scarring makes it harder for oxygen to pass into the bloodstream, leading to breathlessness, especially during activity. The condition typically progresses gradually and can lead to severe breathing difficulties. While the exact cause is unknown, factors like genetics and environmental exposures may contribute. Currently, there’s no cure, but treatments aim to slow disease progression and improve quality of life.