We imagine a world without pulmonary fibrosis.

The Pulmonary Fibrosis Foundation is focused on our mission to act as the trusted resource for all who are affected by this disease. Our signature programs include:
PFF Care Center Network
PFF Patient Registry
PFF Patient Communication Center
PFF Ambassador Program
An international network of support groups and online communities
The PFF Summit
Comprehensive disease education materials

Our expert Medical Advisory Board and the biennial PFF Summit allow us to maintain an ongoing dialogue with physicians, researchers, industry representatives, and the patient community. This creates a collaborative environment that will help us achieve many of our goals.

Our peer-reviewed research program supports projects that improve understanding of pulmonary fibrosis and will lead to successful therapies. We have developed significant relationships with industry partners and upheld our position as the honest broker to inform those affected by pulmonary fibrosis of important scientific breakthroughs.

Health Care

Non Profit

Research

Pulmonary Fibrosis Foundation

Pulmonary Fibrosis Foundation's headquarters in Chicago, IL, United States

Dr. Franck Rahaghi

William Schmidt

Jessica Shore

Seth Klein

Jennifer L. Mefford

Kate Gates

Wayne P.

Development and Fundraising

Leadership Team

Volunteer and Advocacy Programs

Pulmonary Fibrosis Foundation

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Development and Fundraising

Leadership Team

Volunteer and Advocacy Programs

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