Tom Hunter is the Chief Executive Officer at Toronto Seniors Housing Corporation, as well as a CPFF Director since 2019. Normally, each athlete has many events lined up for the summer. This year, the team is excited to collaborate with CPFF for one of the largest events of the summer — the Toronto Triathlon Festival […]
The CPFF Warriors of Hope are composed of 10 members from the Queen’s University triathlon team, which is a student-led varsity club associated with the university in Kingston, ON. The team trains and competes in triathlons throughout the winter semester. Normally, each athlete has many events lined up for the summer. This year, the team […]
The CPFF Warriors of Hope are composed of 10 members from the Queen’s University triathlon team, which is a student-led varsity club associated with the university in Kingston, ON. The team trains and competes in triathlons throughout the winter semester. Normally, each athlete has many events lined up for the summer. This year, the team […]
The Phillips family have been deeply affected by pulmonary fibrosis (PF), with the passing of David Andrew Phillips on June 4, 2021, aged 56 years old. David was the owner of the Avonmore Berry Farm, in Avonmore, Ontario. In his memory, his family created a 5km walk/run through the fields of the farm to raise awareness […]
Help Us Walk, Roll and Run Across Canada (6,818 kms) Join Canadians from coast to coast in the CPFF Virtual Walk, Roll, Run as we make our way across the country. Our goal is to collectively walk across Canada by the end of September 2023. That’s 6,818 kilometers! HOW TO PARTICIPATE Help CPFF raise awareness, […]
Abbie Clarke and her family have been deeply affected by pulmonary fibrosis (PF). She created a walk 7 years ago to raise awareness for the disease. Join the Clarke Walk for PF for this annual in-person walk for PF on September 10th from 10 am to 2 pm MDT. IN-PERSON WALK (10 am to 2 […]
CPFF founder Robert left a monumental legacy of awareness, information, and hope for the pulmonary fibrosis community in Canada and around the world. He established the Canadian Pulmonary Fibrosis Foundation in 2009, less than two years after his own idiopathic pulmonary fibrosis diagnosis and a few months before receiving a double-lung transplant. Robert rallied people […]