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A conversation about PF with Chris Sadleir
On July 23, 2016, Chris Sadleir’s father Rob who was living with pulmonary fibrosis (PF) had a double lung transplant. Thanks to this procedure, he is still with us today […]
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Stan Hendriksen’s Journey with PF
Stan was diagnosed with Pulmonary Fibrosis (PF) in 2016, during a month-long hospitalisation for what was initially believed to be pneumonia. This was a huge shock to Stan, who had […]
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The Clarke Family’s Journey with PF
Pulmonary fibrosis (PF) has played a devastating role in the lives of the Clarke family. Many members of the family have been diagnosed with PF, several of whom have unfortunately […]
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A conversation about PF with Heather and Mark Davidson
CPFF founder Robert left a monumental legacy of awareness, information, and hope for the pulmonary fibrosis (PF) community in Canada and around the world. He established the Canadian Pulmonary Fibrosis […]
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Talking about PF and Oxygen Featuring Todd Georgieff
Breathing is a fundamental human right. Home oxygen therapy is crucial for people living with pulmonary fibrosis (PF), yet many are challenged to get oxygen therapy when needed. In this […]
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Donald Pamenter’s Pulmonary Fibrosis Journey
Nadine Fenton’s father Donald lived a very active and social life, and enjoyed playing tennis, golf, and cards with his friends before being diagnosed with Pulmonary Fibrosis (PF). PF is […]
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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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Cantalope Puckers Up for PF
Cantelope, the mascot for the Trading Post in Ladysmith, British Columbia, supports the CPFF’s work in promoting awareness of pulmonary fibrosis (PF), a debilitating and life-threatening disease. For people with […]
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Caregiving for a husband with slow progressing PF
Carolyn Morton, 74, has seen her husband Dale, 76, cope quite well during his 11-year journey with IPF that, fortunately for them both, has progressed very slowly. She sees her […]