What Is IPF (Interstitial Pulmonary Fibrosis)?
IPF, or Interstitial Pulmonary Fibrosis, is a chronic lung condition in which the delicate tissues between the air sacs of the lungs become inflamed and scarred. Over time, this scarring (fibrosis) makes the lungs stiff and less able to expand and contract, reducing the amount of oxygen that can move from the lungs into the bloodstream. People with IPF often experience a persistent, dry cough and increasing shortness of breath, especially during physical activity.
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