Wescoe Foundation for Pulmonary Fibrosis is a 501(c)3 non-profit organization that provides support, education, resources and advocacy for patients and their families living with Idiopathic Pulmonary Fibrosis (IPF) in order to sustain the highest possible quality of life.
Your kindness supports our pulmonary fibrosis support groups, caregiver support, education programs, lung transplant mentorship program, as well as valuable resources and advocacy for the pulmonary fibrosis community! We are deeply humbled and privileged to be a part of dedicated individuals living with pulmonary fibrosis and their loving families, healthcare professionals, and industry.
Our current and future success of providing our helpful and beneficial programs is achieved by the continued generosity of community supporters! In the coming year, Wescoe Foundation for Pulmonary Fibrosis will be growing and developing our programs throughout the Commonwealth of Pennsylvania, New Jersey and Delaware! We will keep you updated on the exciting progress!
Thank you for your confidence in the Wescoe Foundation for Pulmonary Fibrosis and joining us to make a positive impact in the pulmonary fibrosis community!
Jennifer H. Wescoe, M.Ed., NCC, Executive Director