Elena Russo talks with Bill Schmidt, President and CEO for the Pulmonary Fibrosis Foundation. The Pulmonary Fibrosis Foundation (PFF) mobilizes people and resources to provide access to high-quality care and leads research for a cure so people with pulmonary fibrosis (PF) will live longer healthier lives. The PFF is the nation's leading educational and advocacy organization for all who are affected by pulmonary fibrosis, a life-threatening disease resulting in progressive scarring in the lungs. The Pulmonary Fibrosis Foundation serves patients, caregivers, loved ones and the medical community. For more information on PFF, visit their website.