IPF patient community launches video plea to provinces
IPF Patient Video
Support Ontarians living with IPF - click here to find out how you can help!
IPF Patient Watch List
Because breathing should never be hard work
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Be informed - it could save your life, or the life of a loved one
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Working together for Canadians with pulmonary fibrosis
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Welcome to the home of the Canadian Pulmonary Fibrosis Foundation, a registered Foundation established to provide hope and support for those affected by pulmonary fibrosis.



Visit the Advocacy section of our website to access Provincial Advocacy Packages, and to email your Premier & Health Minister about access to Esbriet.

Find out how YOU can get involved!

Click here

NEW! Click here for the Ontario IPF Patient Watch List
NEW! Click here to download Ontario petition template

What’s Happening

Ontario MPP Statements & Petitions

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Breathing Should Never Be Hard Work

Learn about Robert Davidson’s journey with IPF in his book, “Breathing Should Never Be Hard Work.” A portion of royalties from the sale of books to fund IPF research.

Click here

Heather’s Story

heatherOne day in October 2007, my husband called to tell me the results of tests he had undergone to try and pinpoint the cause of his breathlessness.

He blithely stated: It’s pulmonary fibrosis” obviously knowing nothing about this disease.

I was devastated. I had lost my friend and co-worker Janice to this very disease two years earlier. She had progressed very fast in a few months through the disease, not even getting the chance to be assessed for a lung transplant.

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New! Visit our Patient Education & Support Group Toolkit

Access Toolkit

guide-180This guide provides Robert Davidson’s advice on how patients should manage and advocate for their proper care. It will also answer many of the questions that patients and their caregivers may have, and set them in the right direction to get the answers to other questions.

Download Guide