Founded in 2009, the Canadian Pulmonary Fibrosis Foundation is Canada’s ONLY national organization dedicated to increasing awareness, hope, and funds for people living with pulmonary fibrosis.

Our vision is a world free of pulmonary fibrosis.

Our mission is to improve the lives of Canadians living with pulmonary fibrosis by providing compassionate support, leading advocacy, raising awareness, funding research, and inspiring hope.

Our key objectives in the battle against pulmonary fibrosis are to raise public awareness about this fatal disease, offer support to those affected by pulmonary fibrosis and represent Canadians affected by PF to government, healthcare professionals, the media and the public – to be “the patient voice” for PF.

The CPFF works closely with the medical community and with support from Canadians we hope to achieve our vision, mission and objectives.