Harold Wimmer President and CEO at American Lung Association | Official website
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Patient Daily | Sep 2, 2025

American Lung Association launches free support program for people living with pulmonary fibrosis

The American Lung Association has introduced a new educational program designed to support people living with pulmonary fibrosis (PF) and their families. The announcement comes as part of Pulmonary Fibrosis Awareness Month in September.

Pulmonary fibrosis is a type of interstitial lung disease that leads to scarring in the lungs, making breathing more difficult over time. There are over 200 types of PF, with causes ranging from genetics and medications to autoimmune conditions and environmental exposures. Idiopathic pulmonary fibrosis, the most common form, does not have a known cause. While there is no cure for PF, available treatments can slow its progression and help manage symptoms.

“Pulmonary fibrosis is a life-altering diagnosis that affects not only breathing, but every aspect of a person’s life, so managing this disease can be overwhelming,” said Harold Wimmer, President and CEO of the American Lung Association. “Through our new ‘Learning to Live with PF’ program, we aim to provide individuals with the tools they need to better understand their disease, work with their healthcare providers, and access the latest treatment options. Education and support are key to living well with pulmonary fibrosis, and we are proud to expand on these critical resources through this campaign.”

The new initiative is supported by the Feldman Family Foundation and offers free personalized support for those affected by PF.

“When our dad, Irv Feldman, was diagnosed with pulmonary fibrosis in 2006, there were few resources available to guide us through the challenges ahead. After his passing in 2013, it became our family’s mission to ensure that others facing this disease would not have to navigate it alone. Today, in partnership with the American Lung Association and in honor of Irv, the Feldman Family Foundation is honored to support the Lung Health Navigator program, a meaningful resource for patients, families, and caregivers affected by pulmonary fibrosis,” said Mitchell Feldman, President of the Feldman Family Foundation.

People living with PF or caring for someone who has it can enroll in the free program at Lung.org/navigator or by calling 866-252-2959. More information about pulmonary fibrosis is available at Lung.org/PF.

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