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 […]
Toogood Pond Park
280 Main Street, Unionville, Ontario, Canada
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 […]
Tune into It’s a Beautiful World Program on Cottage Life and YES TV to catch CPFF Pucker Up Challenge TV commercials! Check Cottage Life Schedule in September: https://tv.cottagelife.com/schedule/ Pucker TV […]
Toogood Pond Park
280 Main Street, Unionville, Ontario, Canada
The Khan extended family is proud to host this year’s CPFF Montreal Walk/Run in honour of their father Jawaid Khan who passed away from pulmonary fibrosis. “It’s a struggle, to watch someone experience this devastating disease,” says one of his four daughters, Wendy Khan. “We want to honour our father, as well as all of […]
Gather virtually with other PF patients from across the country to share ideas, experiences, support one another. These facilitator-led patient support group meetings will happen on the first Tuesday of […]
Gather virtually with other PF caregivers from across the country to share ideas, experiences, support one another. These caregiver support group meetings will happen bi-weekly on Mondays at 7:00PM ET. You need to register in advance for this meeting in order to be able to attend. After registering, you will receive a confirmation email containing […]
Join us for our virtual National Support Group every third Tuesday of the month at 3 PM ET to connect and share with members of the PF community! Patients, caregivers, and medical professionals are all welcome. You need to register in advance for this meeting in order to be able to attend. After registering, you […]
Join us for this webinar as CPFF fellow and ILD respirologist, Dr. Daniel Marinescu, explains to us the relationship between pulmonary fibrosis and COVID.
Gather virtually with other PF patients from across the country to share ideas, experiences, support one another. These facilitator-led patient support group meetings will happen on the first Tuesday of every month at 3:00PM ET. The topic for this session will be “Symptom Management/Oxygen”. You need to register in advance for this meeting in order […]
Gather virtually with other PF caregivers from across the country to share ideas, experiences, support one another. These caregiver support group meetings will happen bi-weekly on Mondays at 7:00PM ET. The topic for this session will be “Symptom Management/Oxygen”. You need to register in advance for this meeting in order to be able to attend. […]
Rejoignez-nous pour notre groupe de soutien national virtuel en français à 19h HE pour vous connecter et partager avec les membres de la communauté de la fibrose pulmonaire! Les patients, les aidants et les professionnels de la santé sont tous les bienvenus. Enregistrez-vous aujourd’hui et recevez un courriel de la part de Zoom avec votre […]
Join us for our virtual National Support Group every third Tuesday of the month at 3 PM ET to connect and share with members of the PF community! Patients, caregivers, and medical professionals are all welcome. You need to register in advance for this meeting in order to be able to attend. After registering, you […]
Gather virtually with other PF caregivers from across the country to share ideas, experiences, support one another. These caregiver support group meetings will happen bi-weekly on Mondays at 7:00PM ET. You need to register in advance for this meeting in order to be able to attend. After registering, you will receive a confirmation email containing […]
Gather virtually with other PF patients from across the country to share ideas, experiences, support one another. These facilitator-led patient support group meetings will happen on the first Tuesday of every month at 3:00PM ET. You need to register in advance for this meeting in order to be able to attend. After registering, you will […]
Gather virtually with other PF caregivers from across the country to share ideas, experiences, support one another. These caregiver support group meetings will happen bi-weekly on Mondays at 7:00PM ET. You need to register in advance for this meeting in order to be able to attend. After registering, you will receive a confirmation email containing […]
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 […]
Join us for our virtual National Support Group every third Tuesday of the month at 3 PM ET to connect and share with members of the PF community! Patients, caregivers, and medical professionals are all welcome. You need to register in advance for this meeting in order to be able to attend. After registering, you […]
Assiniboine Park
55 Pavilion Crescent, Winnipeg, Manitoba, Canada
REGISTRATION The CPFF invites you to gather with your community on August 24, 2024 to walk for PF or cheer on those who are walking. Registration is FREE 10:00 am […]
Gather virtually with other PF caregivers from across the country to share ideas, experiences, support one another. These caregiver support group meetings will happen bi-weekly on Mondays at 7:00PM ET. You need to register in advance for this meeting in order to be able to attend. After registering, you will receive a confirmation email containing […]
Walk, Roll and Run Across Canada Join Canadians from coast to coast as we walk, roll, and run across the country for people affected by pulmonary fibrosis. If you have […]
Gather virtually with other PF patients from across the country to share ideas, experiences, support one another. These facilitator-led patient support group meetings will happen on the first Tuesday of every month at 3:00PM ET. You need to register in advance for this meeting in order to be able to attend. After registering, you will […]
Gather virtually with other PF caregivers from across the country to share ideas, experiences, support one another. These caregiver support group meetings will happen bi-weekly on Mondays at 7:00PM ET. You need to register in advance for this meeting in order to be able to attend. After registering, you will receive a confirmation email containing […]
Rejoignez-nous pour notre groupe de soutien national virtuel en français à 19h HE pour vous connecter et partager avec les membres de la communauté de la fibrose pulmonaire! Les patients, les aidants et les professionnels de la santé sont tous les bienvenus. Enregistrez-vous aujourd’hui et recevez un courriel de la part de Zoom avec votre […]
Week 1 Virtual Meetup – MEET & GREETMeet other virtual walkers and pay tribute to your loved or share a cherished memory. Click the “Register Now” button to register to […]
Gabriel Dumont Park
715 Saskatchewan Crescent W, Saskatoon, Saskatchewan, Canada
REGISTRATION (10 AM – 2 PM CST) The CPFF invites you to gather with your community on September 14, 2024 to walk for pulmonary fibrosis or cheer on those who […]
Edworthy Park
5050 Spruce Dr. SW, Calgary, Alberta, Canada
Abbie Clarke and her family have been deeply affected by pulmonary fibrosis (PF). She created a walk 8 years ago to raise awareness for the disease. Join the Clarke Walk […]
Gather virtually with other PF patients from across the country to share ideas, experiences, support one another. Caregivers welcome too! This facilitator-led virtual National Patient Support Group meets on the first and third Tuesdays of the month at 3 PM ET. You need to register in advance for this meeting in order to be able […]
Toogood Pond Park
218 Main Street, Unionville, Ontario, Canada
Heather is walking in memory of Robert Davidson, founder of CPFF and her husband and encourages participants to walk for their loved ones as well. She encourages everyone to follow Robert’s […]
Gather virtually with other PF caregivers from across the country to share ideas, experiences, support one another. These caregiver support group meetings will happen bi-weekly on Mondays at 7:00PM ET. You need to register in advance for this meeting in order to be able to attend. After registering, you will receive a confirmation email containing […]
Parc Angrignon
3500 Boul des Trinitaires, Montréal, QC, Canada
The Khan extended family is proud to host for a second consecutive year the CPFF Montreal Walk/Run in honour of their father Jawaid Khan who passed away from pulmonary fibrosis. “It’s a struggle, to watch someone experience this devastating disease,” says one of his four daughters, Wendy Khan. “We want to honour our father, as […]
Gather virtually with other PF patients from across the country to share ideas, experiences, support one another. Caregivers welcome too! This facilitator-led virtual National Patient Support Group meets on the first and third Tuesdays of the month at 3 PM ET. The topic for this session will be “Nutrition, Exercise, Pulmonary Rehabilitation & Introduction of […]
Gather virtually with other PF caregivers from across the country to share ideas, experiences, support one another. These caregiver support group meetings will happen bi-weekly on Mondays at 7:00PM ET. The topic for this session will be “Nutrition, Exercise, Pulmonary Rehabilitation & Introduction of Book for Review”. You need to register in advance for this […]
Rejoignez-nous pour notre groupe de soutien national virtuel en français à 19h HE pour vous connecter et partager avec les membres de la communauté de la fibrose pulmonaire! Les patients, les aidants et les professionnels de la santé sont tous les bienvenus. Enregistrez-vous aujourd’hui et recevez un courriel de la part de Zoom avec votre […]
Gather virtually with other PF patients from across the country to share ideas, experiences, support one another. Caregivers welcome too! This facilitator-led virtual National Patient Support Group meets on the first and third Tuesdays of the month at 3 PM ET. You need to register in advance for this meeting in order to be able […]
Gather virtually with other PF caregivers from across the country to share ideas, experiences, support one another. These caregiver support group meetings will happen bi-weekly on Mondays at 7:00PM ET. […]
Gather virtually with other PF caregivers from across the country to share ideas, experiences, support one another. These caregiver support group meetings will happen bi-weekly on Mondays at 7:00PM ET. The topic for this session will be “Book for Review & Discussion”. You need to register in advance for this meeting in order to be […]
Rejoignez-nous pour notre groupe de soutien national virtuel en français à 19h HE pour vous connecter et partager avec les membres de la communauté de la fibrose pulmonaire! Les patients, les aidants et les professionnels de la santé sont tous les bienvenus. Enregistrez-vous aujourd’hui et recevez un courriel de la part de Zoom avec votre […]
Gather virtually with other PF patients from across the country to share ideas, experiences, support one another. Caregivers welcome too! This facilitator-led virtual National Patient Support Group meets on the first and third Tuesdays of the month at 3 PM ET. The topic for this session will be “Book for Review & Discussion”. You need […]
Gather virtually with other PF caregivers from across the country to share ideas, experiences, support one another. These caregiver support group meetings will happen bi-weekly on Mondays at 7:00PM ET. You need to register in advance for this meeting in order to be able to attend. After registering, you will receive a confirmation email containing […]
Gather virtually with other PF patients from across the country to share ideas, experiences, support one another. Caregivers welcome too! This facilitator-led virtual National Patient Support Group meets on the first and third Tuesdays of the month at 3 PM ET. You need to register in advance for this meeting in order to be able […]
Gather virtually with other PF caregivers from across the country to share ideas, experiences, support one another. These caregiver support group meetings will happen bi-weekly on Mondays at 7:00PM ET. The topic for this session will be “Gratitude”. You need to register in advance for this meeting in order to be able to attend. After […]
Rejoignez-nous pour notre groupe de soutien national virtuel en français à 19h HE pour vous connecter et partager avec les membres de la communauté de la fibrose pulmonaire! Les patients, les aidants et les professionnels de la santé sont tous les bienvenus. Enregistrez-vous aujourd’hui et recevez un courriel de la part de Zoom avec votre […]
Gather virtually with other PF patients from across the country to share ideas, experiences, support one another. Caregivers welcome too! This facilitator-led virtual National Patient Support Group meets on the first and third Tuesdays of the month at 3 PM ET. The topic for this session will be “Gratitude”. You need to register in advance […]
Gather virtually with other PF caregivers from across the country to share ideas, experiences, support one another. These caregiver support group meetings will happen bi-weekly on Mondays at 7:00PM ET. You need to register in advance for this meeting in order to be able to attend. After registering, you will receive a confirmation email containing […]
Gather virtually with other PF patients from across the country to share ideas, experiences, support one another. Caregivers welcome too! This facilitator-led virtual National Patient Support Group meets on the first and third Tuesdays of the month at 3 PM ET. This session will be and open forum. You need to register in advance for […]
Rejoignez-nous pour notre groupe de soutien national virtuel en français à 19h HE pour vous connecter et partager avec les membres de la communauté de la fibrose pulmonaire!
Rejoignez-nous pour notre groupe de soutien national virtuel en français à 19h HE pour vous connecter et partager avec les membres de la communauté de la fibrose pulmonaire!
If you or someone you care about has been diagnosed with pulmonary fibrosis in the past 6 months , we invite you and your family and friends to attend this meet up.
Rejoignez-nous pour notre groupe de soutien national virtuel en français à 19h HE pour vous connecter et partager avec les membres de la communauté de la fibrose pulmonaire!
Rejoignez-nous pour notre groupe de soutien national virtuel en français à 19h HE pour vous connecter et partager avec les membres de la communauté de la fibrose pulmonaire!
Rejoignez-nous pour notre groupe de soutien national virtuel en français à 19h HE pour vous connecter et partager avec les membres de la communauté de la fibrose pulmonaire!
Rejoignez-nous pour notre groupe de soutien national virtuel en français à 19h HE pour vous connecter et partager avec les membres de la communauté de la fibrose pulmonaire!
Rejoignez-nous pour notre groupe de soutien national virtuel en français à 19h HE pour vous connecter et partager avec les membres de la communauté de la fibrose pulmonaire!
If you or someone you care about has been diagnosed with pulmonary fibrosis in the past 6 months , we invite you and your family and friends to attend this meet up. It can be overwhelming to receive a pulmonary fibrosis diagnosis, and until you become involved with the pulmonary fibrosis community or clinic, it […]
Rejoignez-nous pour notre groupe de soutien national virtuel en français à 19h HE pour vous connecter et partager avec les membres de la communauté de la fibrose pulmonaire!
Rejoignez-nous pour notre groupe de soutien national virtuel en français à 19h HE pour vous connecter et partager avec les membres de la communauté de la fibrose pulmonaire!
Rejoignez-nous pour notre groupe de soutien national virtuel en français à 19h HE pour vous connecter et partager avec les membres de la communauté de la fibrose pulmonaire!
If you or someone you care about has been diagnosed with pulmonary fibrosis in the past 6 months , we invite you and your family and friends to attend this meet up.
If you or someone you care about has been diagnosed with pulmonary fibrosis in the past 6 months , we invite you and your family and friends to attend this meet up.