The Pulmonary Fibrosis Research Enhancement Act (PFREA) has been re-introduced in Congress! This landmark bill, reintroduced on February 13th, establishes a national patient registry, calls for a national oversight program and efforts to increase public awareness of PF! Please note: the bill number has changed from the previous Congress. The NEW bill number is H.R. 1079. Tell your friends and family to call, email or write their congressman. Visit the Coalition for Pulminary Fibrosis website for an easy webform that will send an email for you (for free of course). http://www.coalitionforpf.org/cpf_join.php