First in a series. Shortly after I learned I had idiopathic pulmonary fibrosis (IPF) in January 2017, I came to rely on the Pulmonary Fibrosis Foundation (PFF) as a reliable source of information. That relationship continues today, more than four years after my bilateral lung transplant in 2021. I recently interviewed Scott Staszak, the PFF’s […] The post Talking with the Pulmonary Fibrosis Foundation CEO, part 1 appeared first on Pulmonary Fibrosis News.
