PFF Help Center
For those living with pulmonary fibrosis, obtaining the most accurate and current information can be a challenging and frustrating task. Let us help you find your answers.
The PFF Community Registry: Open for enrollment!
The Pulmonary Fibrosis Foundation is leading the fight by funding promising research and we need your help.
One of our key research programs is the PFF Community Registry. We invite eligible participants to join by completing a series of simple surveys. Your survey responses will be used by researchers to better understand how PF and ILD progress over time, respond to treatments, and how the diseases affect individuals. The more individuals who join and provide responses, the closer we come to a cure.
Eligible participants include:
- Patients living with PF and ILD
- Lung transplant recipients who have had PF or ILD
- Caregivers and biological family members of patients with PF or ILD, including those who have passed away
Enrolling in the PFF Community Registry is entirely online. All you need is internet access. Learn more about this groundbreaking program by visiting the PFF Community Registry homepage.
Have you already enrolled? If so, you can log in to access your account.
Be part of
something special
Find an event and connect with others in the PF community.
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May142024
Northeast Ohio PF Support Group Meeting
This support group is open to all people impacted by pulmonary fibrosis, both patients and caregivers. We welcome those with PF related to any cause and in any stage of disease. Anyone affected by PF may join this group, no matter where they live or where they receive their PF care.
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May152024
Christianacare ILD Support Group
Join the Christianacare ILD Support Group monthly virtual meeting.
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May162024
PFF Voices
This a virtual support group meeting for patients, caregivers, and loved ones of pulmonary fibrosis patients. Healthcare professionals who work with patients are welcome to join as well.
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Clinical Trials
Pulmonary fibrosis patients may find several advantages to joining a clinical trial. Participants may obtain access to a potential new PF medication and receive valuable education about improving their health.
Get involved with the PFF Walk
Join us this year as we walk together toward a cure in Pittsburgh, the NYC Metro area, the San Francisco Bay Area, Chicago, Washington D.C., Dallas, and virtually on National Walk Day!
The Latest News for the PF Community
Explore press releases and articles of interest to PF patients, caregivers and medical professionals.
Read more news →-
April 02, 2024
Broadway Belts for PFF! 2024 Raises Record $516,000 for Pulmonary Fibrosis Foundation
Read Full Article Broadway Belts for PFF! 2024 Raises Record $516,000 for Pulmonary Fibrosis Foundation -
January 22, 2024
Pulmonary Fibrosis Foundation Unveils Groundbreaking Research by PFF Scholars
Read Full Article Pulmonary Fibrosis Foundation Unveils Groundbreaking Research by PFF Scholars -
January 17, 2024
Broadway Stars Take Center Stage in 14th Anniversary Benefit for Pulmonary Fibrosis
Read Full Article Broadway Stars Take Center Stage in 14th Anniversary Benefit for Pulmonary Fibrosis
Educational Materials
Find reliable information and trusted resources that can help you learn about pulmonary fibrosis and live better with PF.
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About the PFF
Read our brochure for a snapshot overview of the Pulmonary Fibrosis Foundation. -
Pulmonary Fibrosis Information Guide
Our comprehensive guide provides reliable information about pulmonary fibrosis, the diagnostic process, treatment options, and more. -
Oxygen Basics Booklet
This booklet provides an in-depth overview of the the basics of supplemental oxygen, including equipment, getting started, Medicare information, and traveling.