Rare Diseases Affect 1 in 12 or Nearly 3 Million Canadians*
Although it should be an effortless act, breathing, for people with a rare lung disease like pulmonary fibrosis, can be a painful, challenging experience. Diagnosis is lagging and access to treatment varies across Canada in part due to lack of awareness and understanding of this disease.
Join us in raising awareness and funds to help advocate for more equitable access to diagnosis, treatment, support, and opportunity for people living with pulmonary fibrosis.
Despite challenges, patients show amazing resilience and courage. Watch patients tell their stories and learn more about pulmonary fibrosis in this Breathless for Change Documentary presented by CPFF.
Pay Tribute to a Rare Individual
Make a donation to send a tribute or memorial card
SHARE A STORY ABOUT A RARE INDIVIDUAL
The CPFF community has experienced the incredible strength of people living with pulmonary fibrosis. These rare individuals showcase hope despite the energy it takes to live life with this devastating disease.
If you know or knew someone living with PF we want to pay tribute to them. Share a photo and few sentences.