Resources on Idiopathic Pulmonary Fibrosis


We have included a sampling of resources that provide general and disease specific information about Idiopathic Pulmonary Fibrosis (IPF). 

Pulmonary Fibrosis Foundation

The Pulmonary Fibrosis Foundation mobilizes people and resources to provide access to high quality care and leads research for a cure so people with pulmonary fibrosis will live longer, healthier lives.

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NORD: Idiopathic Pulmonary Fibrosis

The National Organization for Rare Diseases provides disease information for patients and families on IPF.

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The Lung Association: Idiopathic Pulmonary Fibrosis

The Lung Association is the leading organization in Canada working to promote lung health and prevent and manage lung disease.

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American Thoracic Society: Idiopathic Fibrosis

ATS works to improve health worldwide by advancing research, clinical care, and public health in respiratory disease, critical illness and sleep disorders.

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Action for Pulmonary Fibrosis

A key aim of Action for Pulmonary Fibrosis has been to increase the number of IPF support groups and make to make them accessible to as many patients as possible.

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Duke Division of Pulmonary, Allergy and Critical Care Medicine

The Duke Division of Pulmonary, Allergy and Critical Care Medicine is committed conducting research to better understand, diagnose and treat pulmonary disease.

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