The goal of this program is to vastly expand awareness of PF by holding awareness events and fundraisers across the nation so that we generate, via a grass-roots effort, a much broader national understanding of the implications of PF for everyone, and the impact the disease has on families. Funds raised by this program will go towards serving PF patients, advocating for patient and PF community needs, and funding of research. To join or learn more, click here for more info:
A place to pay tribute to your loved one while raising awareness for the fight against pulmonary fibrosis. Click here for more info
ATS Patient Information Series —Idiopathic Pulmonary Fibrosis
The ATS Patient Information Series is a public service of the American Thoracic Society and its journal the AJRCCM (www.atsjournals.org).
The information appearing in this series is for educational purposes only and should not be used as a substitute for the medical advice of
one’s personal health care provider.
To access this document Click Here
ATS Breathing in America Book
The Breathing in America: Diseases, Progress, and Hope compilation briefly describes respiratory diseases and the progress that is being made in the quest to find their cures.
To access the chapter on interstitial lung disease Click here
ATS Statements, Guidelines and Reports are printed in the American Journal of Respiratory and Critical Care Medicine. These documents are also available in PDF format. You may download one copy of any ATS document; there is no charge for this service. Click here for the 2011 joint IPF statement.