PFF Walk 2024

My son Liam and I, pictured above with my daughter Lauren, will again be walking and fundraising for the Pulmonary Fibrosis Foundation in Chicago on September 14th. With a late start and 28 days to go, we hope to exceed our modest goal toward treatment and a cure for pulmonary fibrosis and idiopathic pulmonary fibrosis.

Join us in supporting this vital cause by donating to our fundraising campaign! With well over 100,000 people in the US living with idiopathic pulmonary fibrosis (IPF), the outcomes are tragically comparable to breast cancer with much less visibility.

The PFF Walk supports efforts to accelerate research to advance improved care for those living with the disease and to provide exceptional support and education resources for patients, caregivers, and family members. Your gift will enable progress and make a valuable contribution toward our vision of a world without pulmonary fibrosis. I appreciate your generosity for the loved ones and families as I enter my 5^th year following diagnosis.

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

We are grateful for your support as we walk together for a cure.

Thankfully, Liam & Bill

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One Week to the Walk!

With 9 days to go before the September 14 Chicago Walk, the patrons at Shiro in Novi organized a donation nearing my current midpoint goal. These friendly traveling merchants had just found success in the local area Renaissance Festival.

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Anonymous September 2024 $500.00
Gary Blalock September 2024 $44.00
Hector and Pamela Garcia September 2024
Brianne Pyrc September 2024 $25.69
JJ Drabicki September 2024 $51.37

Anonymous September 2024 $500.00
Robert Fetherston September 2024 $250.00
Kuhn Inc September 2024 $100.00
Greg Chaplin September 2024 $100.00
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