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.” Read…
Orphan Diseases: Idiopathic Pulmonary Fibrosis
Recent research suggested that the hormone leptin is a potentially promising plasma biomarker of acute exacerbation (AE) and predictor of survival in patients with idiopathic pulmonary fibrosis (IPF). This is the first report associating leptin levels with IPF or AE-IPF, and could hold great potential to improve disease monitoring. The study…
Multidisciplinary Approach to PF Treatment
Pulmonary fibrosis is a lung disease that causes scarring in the tissue of the lungs. It leads to shortness of breath, a persistent dry cough, weight loss, fatigue, and clubbing of the fingers and toes. Read about how you can teach your lungs to improve your breathing. In this…
Top 5 Pulmonary Fibrosis Questions for Your Doctor
If you’ve recently been diagnosed with pulmonary fibrosis, there are probably loads of questions running through your mind.  Here are some of the most important questions you should ask your doctor according to the American Lung Association. 1. “What is pulmonary fibrosis?” Pulmonary fibrosis (PF) literally means scarring of the lungs.
Patients with idiopathic pulmonary fibrosis (IPF) who demonstrate adequate lung volume still have the same rate of lung volume decline as patients with initially lower volumes, and benefit equally from treatment with Ofev (nintedanib), researchers reported. The study, “Nintedanib in patients with idiopathic pulmonary fibrosis and preserved…
What is Lung Auscultation?
Idiopathic Pulmonary fibrosis (IPF) is a difficult disease to diagnose because many of its symptoms are similar to other lung diseases. There is no one single test for the condition. Instead, a series of tests are carried out to diagnose the condition. One test is auscultation.
Allakos recently presented preclinical data demonstrating the potential of its Siglec-8 antibodies in inhibiting components involved in fibrosis in rodent models of lung and skin fibrosis. Â The company believes these antibodies could potentially benefit a wide spectrum of patients with conditions where fibrosis is a major contributor to the…
Essential Oils: Pulmonary Fibrosis
What is Aromatherapy? Have you heard about essential oils? They aren’t anything new. “Essential oil” is basically a different name for an old standby, aromatherapy. There’s plenty of research behind this aromatic trend that shows it can help to alleviate many health conditions. We’ve uncovered some ways essential oils can help you deal…
Personalized Care for Idiopathic Pulmonary Fibrosis
In this PeerView Press video, pulmonologist Dr. David J. Lederer discusses idiopathic pulmonary fibrosis (IPF), with a focus on personalized care through communications and innovative strategies. He is joined by primary care physician Dr. Steven J. Antonini and pulmonary fibrosis patient Robert Brynteson. Read about six lesser-known symptoms…
Building on previous research, scientists at Brown University report that a trio of proteins work together to promote a variety of lung diseases, including idiopathic pulmonary fibrosis (IPF). The findings, published by investigators led by Jack Elias in the journal Nature Communications, appeared in the article “IL-13Rα2 Uses TMEM219 In…
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