• Patient Education Guide

    People living with pulmonary fibrosis (PF) and their family members often find it difficult to get clear, and consistent information about this disease. The purpose of this guide is to […]

  • CPFF Patient Charter

    The CPFF Patient Charter is a document which sets out a number of patient rights in an effortto create a national standard of care. The Charter makes recommendations to provincialgovernments, […]

  • CPFF Breathless for Change Reports

    CPFF asked the PF community to complete a survey about their experiences living with pulmonary fibrosis, its impact on their lives, and what they needed for the future. Many people […]

  • CPFF Oxygen Access in Canada Reports

    Access to Oxygen in Canada Reports / Rapports de la FCFP sur l’accès à l’oxygénothérapie au Canada Supplemental Oxygen in Interstitial Lung Disease: An Art in Need of Science Oxygen […]

  • CPFF Impact Report Highlights

    CPFF works tirelessly to support patients and caregivers, educate the public and medical community, fund research, and advocate for equitable treatment access. We are grateful for the continued support of […]

  • Burden of IPF in Canada Report

    The Burden of IPF in Canada Report reveals major gaps and disparities in care for Canadians living with idiopathic pulmonary fibrosis (IPF). Developed in collaboration with CPFF and Hoffmann-La Roche […]