Today is National Caregiver Day Every person’s journey with PF is different, and so are the experiences of their family caregivers. Below are the stories of four caregivers, looking after […]

Developing clarity in CT scan analysis for better PF diagnosis We last spoke to Dr. Daniel Marinescu in June of 2021, when he was just completing the first year of […]

People with rare diseases deserve equal access to health care More than 30,000 Canadians are living with pulmonary fibrosis (PF), yet it is considered a rare disease in Canada. February […]

CPFFs 2022 Pulmonary Fibrosis Awareness Month campaign wrapped up at the end of September. And once again, our joint efforts have achieved great results. You’ll want to watch our wrap-up video today with detailed results and plenty of participant photos.

CPFFs 2022 Pulmonary Fibrosis Awareness Month campaign wrapped up at the end of September. And once again, our joint efforts have achieved great results. You’ll want to watch our wrap-up video today with detailed results and plenty of participant photos.

It’s Pulmonary Fibrosis Awareness Month! While events and activities are well underway, it’s not too late to get involved in Pulmonary Fibrosis Awareness Month. Register for our national “virtual” walk, and add your kilometres to the national total. We’re aiming for a walk across the country – a total of 6,818 kilometres. A few community…

Set up your own event, or support someone else’s, during Pulmonary Fibrosis Awareness Month in September. Whatever the challenge, Canadian Pulmonary Fibrosis (CPFF) supporters have always risen to the occasion to raise awareness, hope and funds for people living with pulmonary fibrosis. This is especially true during Pulmonary Fibrosis Awareness Month in September. This year a…