This year I am joining Team PFF. I am proud to help lead the way toward a world without pulmonary fibrosis (PF). Please join me as I raise funds and awareness to benefit the Pulmonary Fibrosis Foundation (PFF).

In the Fall of 2024, I was diagnosed with Interstitial Lung Disease (ILD); since then, I have been on a journey of discovery, learning more about both myself and this disease. My condition in particular is complex: it involves ILD with autoimmune tendencies, pulmonary fibrosis*, and esophageal scleroderma. I am grateful to be under the care of an amazing team of forward thinking doctors, each with a specialty pertaining to an aspect of my multifaceted condition. 

Equally amazing is the support structure I have in place to accompany me through this illness, beginning with my two daughters, Elizabeth and Cecilia. The strength, courage, fortitude, and faith with which they have shouldered my diagnosis and care is remarkable! Their unwavering encouragement and resilience have bolstered me. My immeasurable gratitude to all my friends and family who have also walked step-in-step thus far: I love you all!

Now, I come to you, my extended friends and family, and ask you to join me in my fight to improve the quality of life for myself and all those who experience this devastating disease. Research is still rather limited, and to expand the scope, I graciously ask you to consider making a kind and thoughtful donation, so that the years of expectancy double and triple over the coming decade(s). I, for one, plan on being here to see the fruits of your generosity!

Your support—whether it be monetary and/or by sharing this fundraiser with others—is tremendously appreciated. May God bless you! 

* Pulmonary fibrosis is a condition that causes lung tissue to become thickened, stiff, and scarred. The lungs eventually lose their ability to transfer oxygen into the bloodstream, making everyday activities such as breathing and walking extremely difficult. It is a progressive disease, with no known cure, which means it tends to worsen over time. Every individual diagnosed with pulmonary fibrosis has a unique experience with the disease, and there is no “standard” or expected clinical course. Over 250,000 Americans are living with PF today. Approximately 50,000 new cases are diagnosed each year.

But we can't do this without you! Only with your support can we keep the PFF's mission active. Please click the "Donate" button to make your gift today. Thank you again for your generous support!

For more information on how your support will make a difference in the lives of PF patients and their families, please visit www.pulmonaryfibrosis.org.