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Pulmonary Fibrosis – From Invisible to Unmissable with Dr Giovanni Ferrara
Pulmonary fibrosis (PF) is often called an invisible disease, yet this progressive, incurable lung condition profoundly impacts patients and families and often goes undetected until it’s advanced. In this video, Dr. Giovanni Ferrara, a leading respirologist, shines a spotlight on pulmonary fibrosis and the urgent need for awareness, research, and early diagnosis. Learn: Pulmonary fibrosis…
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Lung Transplant in 2025: A Review for Patients with Pulmonary Fibrosis – Dr. Ciaran Scallan
In this informative video, Dr. Ciaran Scallan, respirologist and lung transplant specialist with the University of Toronto Lung Transplant Program, shares an in-depth look at the lung transplant journey for people living with pulmonary fibrosis (PF) — from referral and eligibility to life after transplant. He’s joined by Mark Ashcroft, a PF patient and double…
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Nerandomilast in IPF and PPF, a New Option On the Horizon – Dr. Shane Shapera
The content of this presentation reflects the views and opinions of the presenter alone and does not necessarily represent those of any organization. CPFF and the presenter have not received any funding or support from any company in the creation of this video. **Nerandomilast is an investigational product still under development and has not received…
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CPFF Bold Hope and Bright Impact
Inspired by our founder Robert Davidson, the Canadian Pulmonary Fibrosis Foundation (CPFF) is building brighter futures for over 30,000 Canadians living with pulmonary fibrosis.
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FCFP – Formidable espoir. Impact profond
Inspirée par son fondateur Robert Davidson, la Fondation canadienne de la fibrose pulmonaire (FCFP) œuvre à bâtir un avenir plus lumineux pour plus de 30 000 Canadiens vivant avec la fibrose pulmonaire.
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The Heart of Volunteering with the Canadian Pulmonary Fibrosis Foundation
In this uplifting video, Canadian Pulmonary Fibrosis Foundation (CPFF) volunteer Minh Nguyen shares why giving his time is so rewarding.
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My Hero
He loved me unconditionally. He was kind, supportive and everyone loved him. The hardest and most loyal worker. Always smiling and laughing.
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Bruce Lonergan stepped up to help others cope
Although Bruce Lonergan, 64, has lived with IPF for more than seven years now, he has been fortunate that his disease has progressed quite slowly. The side-effects from anti-fibrotic medications have had the greatest impact on his life, rather than symptoms of the disease itself. “When I listened to others during CPFF’s national support group…
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Debbie Homik finds purpose helping people living with pulmonary fibrosis
From early clinical trials of anti-fibrotic drugs to the Winnipeg Walk for PF, respiratory therapist and dedicated volunteer Debbie Homik is connected, in so many ways, to people living with pulmonary fibrosis (PF).
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CPFF Hope Breathes Here Walks for Pulmonary Fibrosis
Step into the heart of CPFF Hope Breathes Here Walks for Pulmonary Fibrosis. This video shows our incredible community coming together to support people affected by this challenging lung condition. Feel the energy, see the smiles, and see the hope and connection. We walk for breath, we walk for change, and we walk together so…
