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Living with Idiopathic Pulmonary Fibrosis – Meet Zelick
After complaining of a persistent cough during a regular check-up, 66-year old Zelick was diagnosed with idiopathic pulmonary fibrosis (IPF). Watch his story.
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Provincial Resources
Pulmonary Fibrosis Provincial Resource Guides Find pulmonary fibrosis resources within your province in these handy guide books including support for palliative care, home oxygen programs, MAiD, lung transplants, psychologists, personal […]
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CPFF Reports
Breathless for Change Report 2022 / À bout de souffle pour du changement 2022 Breathless for Change Report Highlights 2022 / À bout de souffle pour du changement faits saillants 2022 Breathless for Change […]
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CPFF Volunteer Resources
Volunteer Resources
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Covid-19
Information about COVID-19 and various international, national, provincial and local statistics and policies are changing constantly. The following are some trustworthy resources for COVID-19 information and updates. For more local […]
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CPFF Support Group Resources
Idiopathic pulmonary fibrosis (IPF) support and education groups play an important role in helping individuals living with IPF, their families and friends better understand the disease and their options to […]
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Managing PF
Having pulmonary fibrosis can be an emotional rollercoaster. Friends and family are likely unfamiliar with the disease. It may be difficult to discuss your situation with others. As everyday activities […]
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Manitoba Palliative Care
Learn about palliative care for people living with pulmonary fibrosis in Manitoba.
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Living and Dying Well in Alberta
Learn about palliative care for people living with pulmonary fibrosis in Alberta.
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Palliative Care in Canada
Laurel Gillespie, CEO of the Canadian Hospice Palliative Care Association (CHPCA) discusses palliative care in Canada.
