PFF Walk - Washington, D.C.
Thank you for your support of the PFF Walk - Washington, D.C.!
Fundraising pages will remain active until the end of the year. Post-Walk is a great time to update your page with photos from the Walk and thank your donors!
PFF Walk Incentive Program
Fundraising pages will remain active through the end of the year and prizes can be redeemed through December 31, 2024! To check your fundraising totals and see what you qualify for, please log in to your fundraising dashboard!
Eligible fundraisers will receive a redemption email with instructions on how to claim their prize. If you have questions or need more information, please send us an email at PFFWalk@pulmonaryfibrosis.org.
Please note: Thank you gifts are determined by individual fundraising totals. All PFF Walk participants who register and raise funds are eligible to redeem a gift from their highest level achieved (or under). Team fundraising totals and non-registered donors do not qualify for this program. The PFF reserves the right to substitute a gift of equal or greater value or to change the gifts at any time.
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Highlights from the PFF Walk - Washington, D.C.
View the full gallery of images on our official Flickr account.
Fundraising resources
Use these resources to help get your fundraising campaign started and make it a success!
Walker Guide
Our step-by-step guide to a positive Walk experience!
Team Leader Guide
Check out this guide for easy steps on building a team for the PFF Walk!
Mission Video
Watch and share this video to strengthen your fundraising efforts!
Thank you to our sponsors!
National Gold
National Silver
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National Bronze
Care Center Network Partner
Washington, D.C. Bronze
Additional ways to get involved
Become an advocate
Want to raise your voices for issues that directly affect the pulmonary fibrosis community, like oxygen access or research funding? Take action and join the PFF Advocates today!
Join the PFF Community Registry
You can contribute to tangible, positive change and improvements in research, advocacy, education, and practice to help us find a cure. Learn more and sign up today!
Attend Broadway Belts for PFF!
Returning for one night only, Broadway Belts for PFF! Join us on
March 10 live at Sony Hall in New York City or tune in virtually for this once-in-a-lifetime performance.
Share your story
We know that everyone who participates in the PFF Walk has a story to tell and we'd love to hear yours! You may even be featured on the PFF social media channels.
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.
Questions?
For more information, please contact PFFWalk@pulmonaryfibrosis.org or give us a call at 855.WalkPFF (855.925.5733).