By actively engaging the PF community, the Pulmonary Fibrosis Foundation has developed essential programs available to those living and working with 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 community 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
- 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.
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