Pulmonary Fibrosis Community Steps Toward a Cure with PFF Walk 2025
In celebration of the PFF's 25th anniversary, this year's Walk includes a special community tent featuring opportunities to connect with others impacted by PF, access educational resources, and pick up exclusive PFF Walk-themed swag – stickers, beads, pins and more. Walk events will take place at the following locations and virtually –
June 21 ,Pittsburgh ,North Shore Riverfront Park August 2 , NYC Metro,Liberty State Park Sept. 6 ,Bay Area ,Little Marina Green Sept. 20 ,Chicago ,Montrose Harbor Sept. 27 , National Walk Day, VirtualSept. 27 ,Washington D.C ., National HarborOct. 18 ,Dallas , The Sound at Cypress Waters
"While PF is a debilitating lung disease, our community is driving significant progress toward a brighter future through research and education," said
The PFF Walk unites people living with PF, caregivers and family members, lung transplant recipients, and all community members. Each Walk features one- and two-mile course options. The events also include activities and entertainment, including music, food and family fun.
In addition to the walks in six cities, National Walk Day on
Registration for the PFF Walk is free. Walkers who raise
About the Pulmonary Fibrosis Foundation
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)
Contact:
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SOURCE The Pulmonary Fibrosis Foundation
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