PFF Walk 2025   ○   The Wild Bill's

Leilah Smith

Together toward a cure for pulmonary fibrosis

Your donation gets us one step closer to our goal

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My father, nicknamed Wild Bill, passed away on September 17th, 2022 from Idiopathic Pulmonary Fibrosis. It is a rare genetic disease and there is not yet a cure. In fact, they have not yet isolated the specific gene that activates the disease.

As research grant funding gets a dramatic cut in support from the government, it is more important than ever to help support these organizations who help find cures for such brutal diseases like these!!!

I am proud and excited to be fundraising for the Pulmonary Fibrosis Foundation (PFF) as we walk together toward a cure for pulmonary fibrosis (PF) at the PFF Walk 2025 in Chicago, Illinois in September. 

Please, join me in supporting this vital cause by donating to my fundraising efforts. I know my father would have appreciated it.

My father would have been 67 years old this year, so my goal is to raise $670. 

The PFF Walk supports the Foundation’s efforts to accelerate research, advance improved care for those living with the disease, and provide unequaled support and education resources for patients, caregivers, family members, and healthcare providers.

Your gift will power progress, and I appreciate your generosity in supporting a cause that is so very important to me!

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

I am grateful for your support as we walk together toward a cure.

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