Build a team, raise funds and lead the way towards a world without pulmonary fibrosis with us on Saturday, September 9th in Chicago, IL or virtually.
Patients, families, caregivers, and friends are invited to join for a one- or three-mile walk on the city’s magnificent lakefront in the historic Lincoln Park neighborhood. The PFF walk offers an unprecedented opportunity to unite the community and provide a platform to share your story with others who have been affected by pulmonary fibrosis.
Ways to Participate
Walk with us in Chicago
Start a team: Recruit your friends, family, colleagues and neighbors to walk with you in Lincoln Park! Click the “create a team” button on the top left corner of the page.
Join a team: If you were recruited by someone to walk, click the “join a team” button, search for the team name and proceed with your registration. Don’t know the team name? You can view teams on the right hand side of the screen in the gray box labeled “fundraiser.”
Register individually: Individual registrations are also available for the walk. Click the “participate as an individual” button and proceed with setting up your page. You can create a team later by emailing Amy or make friends with other families who are affected by pulmonary fibrosis on the day of the event.
Can’t make it to Lincoln Park – no problem! Join forces with other patients, families and friends of the pulmonary fibrosis community and register for our virtual walk. You can create a team, join a team, or start an individual page as outlined in the instructions above. You can even log your miles in a park near your house on a day that’s convenient for you!
Join the committee
If you’d like to get more involved in the planning, fundraising, recruitment, and sponsorship behind the PFF Walk, please contact Amy by email, email@example.com, or phone, 312.878.2351, to learn more about roles on the committee.
Sponsor the PFF Walk
Sponsorship opportunities are available for this event. For more information, please contact Amy by email, firstname.lastname@example.org, or phone, 312.878.2351.
The Pulmonary Fibrosis Foundation (PFF) mobilizes people and resources to provide access to high quality care and leads research for a cure so people with pulmonary fibrosis will live longer, healthier lives. We are focused on our mission to act as the trusted resource for all who are affected by this disease. Your support funds crucial research, increase awareness, and sustain vital programs that help people with PF and their families live better lives.
Our signature programs include:
The Pulmonary Fibrosis Foundation rates among top charities in the U.S. The PFF has a four-star rating from Charity Navigator, and for the second consecutive year, the PFF meets all 20 of the Better Business Bureau's accreditation standards. For more information, please visit our website.
Offline Check or Cash Donations
Checks or cash collected offline can be sent to our office via the address below. Please also include the offline donation tracker (for multiple gifts) or the mail-in donation form (for one or two gifts).
Pulmonary Fibrosis Foundation
230 E Ohio St., Suite 500
Chicago, IL 60611
Identify potential donors with our sphere of influence tool
Raise $500 (or more!) in eight easy steps with helpful fundraising tips
Track offline donations with this simple donation tool
Interact with Us on Social Media
Share the PFF Walk with your network through our Facebook event!
Questions? Contact Us!