Funds support those suffering from pulmonary fibrosis
“It is so heartwarming to see all the walks across the country this year. When my late husband Robert Davidson started CPFF in 2009, his dream was to fundraise for research and support others who suffered from pulmonary fibrosis (PF). He would be so proud to see how much the foundation has grown and what has been achieved in 15 years,” said Heather Davidson.
When Robert was diagnosed, there were no PF support groups in Canada; today, there are 25. Furthermore, two medications are now available to help slow the progression of PF, with three more in clinical trials that hold the potential to be life-changing.
For more information about pulmonary fibrosis—a devastating lung disease that irreversibly damages lung tissue and leaves patients dependent on oxygen—or to make a donation, visit www.cpff.ca.
Photo: CPFF Executive Director Sharon Lee (2nd from right) was joined by local dignitaries at this year’s event.

