Idiopathic pulmonary fibrosis (IPF) is a rare and chronic lung disease that causes scarring of the lung tissue which leads to difficulties in breathing and a persistent dry cough. Because it only affects only up to 43 people in every 100,000, it is designated as an “orphan disease.”
The definition of “orphan disease” is explained in this Boehringer Ingelheim Idiopathic Pulmonary Fibrosis video. IPF prevalence is thought to be much higher than the registered 3 million patients worldwide because it is often misdiagnosed.
Pulmonary Fibrosis News is strictly a news and information website about the disease. It does not provide medical advice, diagnosis or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or another qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website.
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