News

Paul Fogelberg, longtime PF advocate and Director of Pulmonary Fibrosis Advocates, which is now working with the Pulmonary Fibrosis Foundation, and Sen. Amy Klobuchar, D-Minn., were honored at the Everylife Foundation for Rare Diseases Rare Voice Awards ceremony on November 5 in Washington D.C.

Howard Honors Memory Of His Father In NFL’s My Cause, My Cleats Campaign

Physicians and researchers presented the latest scientific research into the numerous types of pulmonary fibrosis (PF), giving hope to nearly 900 patients, caregivers, and industry professionals at the Pulmonary Fibrosis Foundation’s (PFF) biennial PFF Summit last week in Nashville, Tenn.

WASHINGTON, Nov. 14, 2017 /PRNewswire-USNewswire/ -- On behalf of millions of Americans with rare diseases, a coalition of 36 patient organizations united to oppose the Senate's proposed weakening of the Orphan Drug Tax Credit as part of the Tax Cuts and Jobs Act.

The United States Senate unanimously voted to declare September 2017 Pulmonary Fibrosis Awareness Month.

The Pulmonary Fibrosis Foundation (PFF), the nation’s leading pulmonary fibrosis (PF) advocacy organization, has announced its keynote speakers for the upcoming PFF Summit 2017. The biennial meeting will take place Nov. 9-11, at the Omni Nashville Hotel in Nashville, Tenn.