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April 2024
Our April Newsletter is out! Get the latest updates on new Robert Davidson fellows, insights on liquid oxygen, and an opportunity to celebrate the caregivers that support each and every PF patient.
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March 2024
CPFF March Newsletter is here! Meet new CPFF staff, learn about chronic cough research, Rare Disease Campaign activities, advocacy initiatives, and more.
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February 2024
The Canadian Pulmonary Fibrosis Foundation (CPFF) is pleased to announce the appointment of Todd Georgieff as Chair of its Board of Directors during the CPFF Annual General Meeting held on January 26, 2024 in Toronto, Ontario.
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December 2023
A message from our outgoing Board Chair It was six years ago in December 2017, that I met with Robert and Heather Davidson, Barb Barr and George Kaminsky, to talk […]
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November 2023
You did it! We all did it. We surpassed our Pulmonary Fibrosis Awareness Month goal of $100,000 by $500. “Congratulations to us all,” says Sharon Lee, CPFF Executive Director. “With […]
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October 2023
Breathing has to be a fundamental human right and equal for all Canadians For people living with PF and their families, receiving oxygen therapy is often critical in functioning day […]
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September 2023
Embrace hope this September There are so many ways to “Embrace Hope” during Pulmonary Fibrosis Awareness Month, from taking the Pucker Up Challenge to participating in a community or virtual […]
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August 2023
CPFF Robert Davidson Fellowships fill a gap in ILD care A recent graduate of CPFF’s Robert Davidson Fellowship, Amanda Grant-Orser, told the CPFF Board during a presentation in June, that […]
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June 2023
A unique case sparks a passion for ILD research and patient care “My interest in ILD began during my respirology elective, when I cared for a 30-year-old man with PPFE […]
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May 2023
CPFF research investment surpasses $2 million With the awarding of the 2023-2024 CPFF Robert Davidson Fellowships, the foundation’s investment in research totals $2.16 million, more than doubling during the last […]