I'm walking for the Pulmonary Fibrosis
Foundation
I have Idopathic Pulmonary Fibrosis (IPF). I am fortunate that this disease has little impact on my life, at the moment. The same cannot be said for others with Pulmonary Fibrosis. The PFF provides support, education, advocacy, and more for those afflicted, their families, and care givers.
Last year I walked and with your help raised $2,445.43 to benefit the Pulmonary Fibrosis Foundation's work. This year my goal has doubled to $5,000.
This year I have created a team, "Team Walking Scotts" who will be partcipating in the National Walk Day on Saturday September 26th. If you would like to join our team either follow this link here.
The PFF Walks are being held nationwide to raise funds and build awareness as we walk together toward a cure!
More than 250,000 Americans are living with pulmonary fibrosis (PF) alone, and funds raised by the PFF Walk help accelerate research, empower our community, and transform care so that everyone with PF and interstitial lung disease (ILD) can live a better life.
And you can help!
Your gift will power progress in the search for a cure and make a meaningful impact in the lives of patients and their families. To get started, click on the "Donate Now" or the "Register For This Event" button on the right-hand side.
Visit PFFWalk.org to learn more about the PFF Walk. To learn more about the impact of your support, please visit pulmonaryfibrosis.org.
Thank you!