About the PFF Walk
Together toward a cure for pulmonary fibrosis.
Thank you for joining us for another incredible PFF Walk season! Together, we have raised a record-breaking $1.1 million and counting to accelerate research, to advance improved care for those living with pulmonary fibrosis and idiopathic pulmonary fibrosis, and to provide unequaled support and education resources for patients and their families. Whether you live with PF, have received a lung transplant, or are a caregiver, family member, friend, or healthcare professional, we celebrate you and your work toward our collective goal: a cure for pulmonary fibrosis. Thank you for bringing us one step closer to a cure in 2024!
Thank you for joining us at the PFF Walk!
Pittsburgh | North Shore Riverfront Park | July 20, 2024
NYC Metro | Liberty State Park | August 3, 2024
Bay Area | Little Marine Green | September 7, 2024
Chicago | Diversey Harbor | September 14, 2024
National Walk Day | Virtual | September 28, 2024
Washington, D.C. | National Harbor | October 12, 2024
Dallas | The Sound at Cypress Waters | October 19, 2024
Registration is still open for National Walk Day and fundraising will continue through the end of the year. Join us in making an impact!
Your support brings us one step closer to a cure.
Get involved
Make a difference by donating to support the mission of the PFF!
You can make the PFF Walk possible! National, single-market, and exclusive opportunities are available. Contact us for more information.
Provide support for the PFF Walk by volunteering! Fill out our interest form to learn more about our day-of volunteer opportunities.
About the Pulmonary Fibrosis Foundation
At the Pulmonary Fibrosis Foundation, we are dedicated to making a difference in the lives of those affected by pulmonary fibrosis (PF), a form of interstitial lung disease (ILD). Pulmonary fibrosis is a process that causes lung scarring, in which fibrotic tissue blocks the movement of oxygen from inside the tiny air sacs in the lungs into the bloodstream. Low oxygen levels, and the stiff scar tissue itself, can cause people with pulmonary fibrosis to feel short of breath, particularly when walking and exercising. Over 250,000 Americans are living with PF today. Approximately 50,000 new cases are diagnosed each year and as many as 40,000 Americans die from idiopathic pulmonary fibrosis (IPF) each year.
As the largest organization committed to raising awareness and providing support, our mission 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 healthcare providers.