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CPFF Documentary – Breathless for Change
Many of us take breathing for granted. Although it may seem like an effortless act, for people with a rare disease like pulmonary fibrosis (PF), breathing can be a painful […]
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A conversation about pulmonary fibrosis featuring Angie Ortlieb
Angie Ortlieb’s dad Bruce was diagnosed with pulmonary fibrosis (PF) in 2011. Like many, they had never heard about this disease before. Bruce was a hard worker and a proud […]
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Patricia Meadows’ Pulmonary Fibrosis Journey
Patricia Meadows from Calgary, Alberta, lives with idiopathic pulmonary fibrosis (PF) with an underlying undetermined auto-immune disease. Prior to her diagnosis, Patricia was an active adventurer. She loved to hike […]
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Climbing Mount Kilimanjaro in Memory of his Father
I started a fundraiser in the memory of my father Clare ‘Charlie’ Taylor who lived with pulmonary fibrosis for the last decade of his life. Watching my dad get on […]
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George Kaminsky was a great support to others facing PF
The Board of CPFF is saddened to share the news that former Board member George Kaminsky passed away on December 11, 2022. He served on the Board for several years […]
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Being a PF caregiver has its challenges and rewards
Asked what advice she’d give to other caregivers living with people with pulmonary fibrosis (PF), Beth Garbutt, 61, has a few tips: “Join a support group. Learn more. Ask questions. […]
