PFF in the News

Pulmonary Fibrosis Foundation Launches Research Fund to Cure Pulmonary Fibrosis
10/17/2011

New Awards Totaling $200,000 to be Offered in 2012;
Deadline for Letters of Intent is November 17, 2011

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Pulmonary Fibrosis Foundation to Fund Further Therapeutic Evaluation Studies for Compugen-Discovered Drug Candidate
10/12/2011

Potential use of CGEN-25009 for treatment of idiopathic pulmonary fibrosis previously demonstrated in animal disease model

Studies to be undertaken at the University of Pittsburgh School of Medicine and the Dorothy P. and Richard P. Simmons Center for Interstitial Lung Disease

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Pulmonary Fibrosis Foundation Announces American Thoracic Society Endorsement of Inaugural Scientific Conference and Co-Chairs for Anniversary Dinner
9/23/2011

Pulmonary Fibrosis Foundation On Course to Achieve Major 2011 Initiatives

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Late Patient’s Husband, Fellow Advocates Ask Congress for Help for Lethal Lung Disease
9/20/2011

Ninth Annual National Pulmonary Fibrosis Awareness Week Sept. 18-24

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Bi-Partisan Congressional Coalition Reaches Across the Aisle to Introduce the Pulmonary Fibrosis Research Enhancement Act in the U.S. Congress
7/12/2011

Landmark Legislation Will Coordinate and Expand National Research on Pulmonary Fibrosis

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Jersey Mike’s Subs in Chicagoland Area Host Fundraiser June 6 To Benefit the Pulmonary Fibrosis Foundation
5/31/2011

20 Stores Donate 20% of Proceeds to Raise Funds and Awareness

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Pulmonary Fibrosis Foundation is an Official Charity for the Manchester Marathon!
9/15/2010

The Pulmomary Fibrosis Foundation is an Official Charity of the Manchester City Marathon in Manchester, NH being held on Sunday, November 7, 2010. This marks the 4th Annual running of the Manchester City Marathon. The MCM is a challenging Boston Qualifier that takes runners on a scenic trip through the historic mill district of the Granite State's largest city. Runners in the full and half marathon will enjoy an exhilarating climb to one of the city's highest points for fabulous views of the Queen City, surrounding areas, and beautiful fall foliage.

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IPF Patient Bob O'Rourke is featured on NPR's "All Things Considered"
8/25/2010

Breathing New Life Into Lung Disease Awareness
by Joe Palca

To listen to the interview click this link: http://www.npr.org/templates/story/story.php?storyId=129376945#

Robert O'Rourke has idiopathic pulmonary fibrosis, and he wants the world to know about it.

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Pulmonary Fibrosis Foundation Supports Goals of 2010 National Pulmonary Fibrosis Awareness Week
8/19/2010

PFF Call on Patients, Families, and Supporters to Contact Congress and Urge Support for S. 3703 and H.R. 1079

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Pulmonary Fibrosis Foundation Proudly Endorses the Introduction of the Pulmonary Fibrosis Research Enhancement Act in the United States Senate
8/4/2010

CHICAGO, Aug. 4 /PRNewswire-USNewswire/ -- The Pulmonary Fibrosis Foundation (PFF) today announced that the Pulmonary Fibrosis Research Enhancement Act (PFREA) was introduced in the United States Senate.

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