• September 2022

    It’s Pulmonary Fibrosis Awareness Month! While events and activities are well underway, it’s not too late to get involved in Pulmonary Fibrosis Awareness Month. Register for our national “virtual” walk, and add your kilometres to the national total. We’re aiming for a walk across the country – a total of 6,818 kilometres. A few community walks and events have taken place already, but there are still some outstanding. Check them out and consider taking part.

    September 2022
  • August 2022

    Set up your own event, or support someone else’s, during Pulmonary Fibrosis Awareness Month in September. Whatever the challenge, Canadian Pulmonary Fibrosis (CPFF) supporters have always risen to the occasion to raise awareness, hope and funds for people living with pulmonary fibrosis. This is especially true during Pulmonary Fibrosis Awareness Month in September. This year a couple of folks held advance events during the summer. John Dennis helped us kick off early awareness efforts in June with his “I ride for you and me,” campaign, riding his electric bike along PEI’s The Island Trail. To date, John’s campaign has raised more than $25,000 and garnered plenty of local media attention and social media followers.

    August 2022
  • June 2022

    CPFF’s 2022 patient and caregiver survey is open for your responses until this Friday, June 10. Don’t miss this opportunity to share your experiences of living with pulmonary fibrosis so that we can create future plans that will help us to serve you better than ever. It takes about 15 minutes to complete the survey.

    June 2022
  • May 2022

    CPFF announces 2022-2023 Robert Davidson Fellowships Advancing research and developing more respiratory specialists to improve care, as well as expand access to care, for people living with pulmonary fibrosis (PF) […]

  • April 2022

    Help us get nintedanib for all who need it We are very pleased to share the news that Alberta became the first province on April 1, 2022, to list on […]

  • March 2022

    Celebrating rare individuals We are all unique individuals tied together by our dedication to a better life for people living with pulmonary fibrosis (PF). We each deal with the challenges […]

  • February 2022

    Let’s breathe hope into 2022 A message from Sharon Lee, Executive Director, CPFF For our first issue of Hope Breathes Here in 2022, I am pleased to share with you […]

  • December 2021

    Hope breathes here A message from CPFF Board Chair Kirk Morrison This has been another very challenging year as we dealt with the continued anxiety and restrictions of the pandemic, […]

  • November 2021

    Upcoming webinar explains new x-ray technology that may detect PF earlier We know that one of the biggest challenges of pulmonary fibrosis is obtaining a timely diagnosis. Most patients wait […]

  • October 2021

    Thank you one and all! Despite the continuing restraints of a second year of the pandemic, this year’s virtual Pulmonary Fibrosis Awareness Month campaign in September raised more than $43,000 […]