Interstitial Lung Disease (ILD) & Idiopathic Pulmonary Fibrosis (IPF)

Leading the way in Interstitial Lung Disease care.

Interstitial Lung Disease (ILD) is a large group of lung disorders associated with inflammation and scarring of lung tissue. It is comprised of over 100 disorders that include Idiopathic Pulmonary Fibrosis (IPF), Hypersensitivity Pneumonitis, Sarcoidosis, Connective Tissue or Auto Immune related ILD, and many others. The inflammation and scarring of the lungs caused by this group of diseases makes it harder for your lungs to take in oxygen, often leading to shortness of breath and a persistent dry cough. The diseases can be difficult to diagnose and vary from patient to patient. That is why the Interstitial Lung Disease Clinic at MUSC has the most current diagnostic and therapeutic modalities available. Our team takes a multidisciplinary approach to create a care plan that is personalized for you.

Idiopathic Pulmonary Fibrosis is a type of chronic ILD that causes progressive scarring of the lungs, leading to worsening shortness of breath and decreased lung function over time. IPF is more common in men, but it can affect anyone. With expert care and the latest therapies, we help patients with IPF and other forms of ILD breathe easier and live better.