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Pulmonary Fibrosis Foundation Expands Clinical Trial Resources for Patients

The Pulmonary Fibrosis Foundation (PFF) has developed new materials and tools for people living with pulmonary fibrosis (PF) to learn about and enroll in clinical research studies.
17-May-2022 9:05 AM EDT Add to Favorites

Pulmonary Fibrosis Foundation Research Explores Quality and Access to Patient Care

The Pulmonary Fibrosis Foundation announced research results from four studies examining access to care and outcomes for patients living with pulmonary fibrosis and interstitial lung disease.
16-May-2022 9:00 AM EDT Add to Favorites

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Broadway Belts for PFF! Raises Record $475,000

Benefit for Pulmonary Fibrosis Foundation Features Broadway’s Hottest Stars and Supports Thousands with Life-Threating Lung Disease
5-May-2022 1:55 PM EDT Add to Favorites

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Pulmonary Fibrosis Foundation Educates Patients on Supportive Care and Treatments for International Quality of Life Month

The PFF embraces International Quality of Life Month as an opportunity to shine a spotlight on emerging treatments and supportive resources that can improve quality of life for patients affected by pulmonary fibrosis – a debilitating, often...
24-Jan-2022 5:05 PM EST Add to Favorites

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PFF Summit 2021 Achieves Record Attendance, Expands New Therapies, Research, and Clinical Trials

Physicians and researchers presented the latest scientific developments into pulmonary fibrosis and interstitial lung disease at its biennial PFF Summit in November. Registration is still open at PFFSummit.org to view all sessions on-demand through...
7-Dec-2021 11:30 AM EST Add to Favorites

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Pulmonary Fibrosis Foundation Position Statement Recommends Addressing Palliative Care Early in Patient Journey

New Pulmonary Fibrosis Foundation (PFF) position statement advises that pulmonologists who treat patients with pulmonary fibrosis (PF) explore palliative care resources available in their communities to facilitate early referral and better quality...
26-Oct-2021 10:20 AM EDT Add to Favorites

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Pulmonary Fibrosis Foundation To Launch National Walk Day

The nationwide pulmonary fibrosis (PF) community will take a collective step forward to advance research, advocacy, and awareness in the Pulmonary Fibrosis Foundation's (PFF) National Walk Day on Saturday, Sept. 25, during Pulmonary Fibrosis...
1-Sep-2021 1:30 PM EDT Add to Favorites

Focus on “Growing Stronger” for Pulmonary Fibrosis Awareness Month in September

September is Pulmonary Fibrosis Awareness Month, presented by the Pulmonary Fibrosis Foundation (PFF) as a way to drive awareness of pulmonary fibrosis (PF), a debilitating, incurable lung disease. Learn more about the numerous endeavors intended to...
19-Aug-2021 4:35 PM EDT Add to Favorites

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The mission of the Pulmonary Fibrosis Foundation is to accelerate the development of new treatments and ultimately a cure for pulmonary fibrosis. Until this goal is achieved, the PFF is committed to advancing improved care of patients with PF and providing unequaled support and education resources for patients, caregivers, family members, and health care providers. The PFF has a four-star rating from Charity Navigator and is an accredited charity by the Better Business Bureau (BBB) Wise Giving Alliance. The Foundation has met all of the requirements of the National Health Council Standards of Excellence Certification Program® and has earned the Guidestar Platinum Seal of Transparency. For more information, visit pulmonaryfibrosis.org or call 844.TalkPFF (844.825.5733) or 312.587.9272 from outside the U.S.



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