Virtual Wescoe Walk for Pulmonary Fibrosis XV

October 30, 2020 @ 12:00AM — November 1, 2020 @ 11:30PM Eastern Time (US & Canada)

The Wescoe Walk for Pulmonary Fibrosis XV will be held VIRTUALLY throughout the weekend of Friday, October 30-Sunday, November 1. We will be having a virtual raffle, too, as we continue to support our businesses!

Virtual Wescoe Walk for Pulmonary Fibrosis XV image

WALK and BREATHE for the Pulmonary Fibrosis community!

There are currently no tickets available for this event, but you can still make a donation.

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In 2020, The Wescoe Walk for Pulmonary Fibrosis XV we will be celebrating 15 years of raising awareness and educating the community about Idiopathic Pulmonary Fibrosis (IPF). Wescoe Foundation for Pulmonary Fibrosis was created in memory of my Dad, Ron Wescoe. He would be incredibly humbled to know that he has made such a positive influence in the pulmonary fibrosis community.

Throughout the years, we have crossed state lines, created 17 pulmonary fibrosis support groups, a lung transplant mentorship program, carepartners support, education program, awareness efforts throughout the Commonwealth of Pennsylvania. As you know, we can only provide these important and very needed programs because of your support!

This year, we are proudly launching Pennsylvania IPF Patient and Caregiver Support Network.Our support network will expand throughout Pennsylvania to support the pulmonary fibrosis community. We are so excited for this addition to our programs! Stay tuned for a new website and literature as we forge on for patients and families living with IPF.

The Wescoe Walk for Pulmonary Fibrosis XV will be held VIRTUALLY throughout the weekend of Friday, October 30-Sunday, November 1. We will be having a virtual raffle, too, as we continue to support our businesses!

JOIN US! FREE registration is online at www.active.com: Virtual Wescoe Walk for Pulmonary Fibrosis XV from Friday, October 30-Sunday, November 1! Visit our website at www.wescoefoundationforpulmonaryfibrosis to learn more about our growing programs and services!

Help us, help others living with pulmonary fibrosis. We, together, can make a difference!

Warmest regards,

Jennifer Wescoe Singley, M.Ed.,NCC

Executive Director

Wescoe Foundation for Pulmonary Fibrosis