Pulmonary Fibrosis Foundation

September is Pulmonary Fibrosis Awareness Month, and for more than 25 years, the Pulmonary Fibrosis Foundation has been accelerating research, empowering our community, and transforming care for those living with PF. A diagnosis of Pulmonary Fibrosis can leave some people feeling lost and confused. But the Foundation is here to help. With us this morning to talk more about the Pulmonary Fibrosis Foundation and the work they are doing for people living with PF is Seth Klein, the Chief Development Officer of the organization.

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