Pulmonary Fibrosis (PF)
Pulmonary fibrosis is a condition in which the lungs develop an excess of connective tissue (or fibrosis), known as “scarring” of the lung. As a result, the lungs become thick and stiff over time, and breathing becomes difficult. Other symptoms may include chronic cough, fatigue, chest discomfort, and loss of weight and appetite.
Pulmonary fibrosis is usually, though not always, the resulting effect of other diseases or conditions. Potential causes range from rheumatoid arthritis to inhalation of harmful substances such as asbestos and cigarettes.
Roberta Latten – Patient Testimonial from Caring Voice Coalition on Vimeo.
- Shortness of breath
- Chronic dry and hacking cough
- Fatigue and weakness
- Chest discomfort
- Loss of appetite and rapid weightloss
Imaging tests such as chest x-ray and computerized tomography (CT) scans are able to determine if one has pulmonary fibrosis. Consult your doctor if you are experiencing symptoms.
No drugs are currently FDA-approved for the treatment of IPF.
