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  • CPFF Virtual Walk, Roll, Run

    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 […]
  • National Patient Support Group – September 3

    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 […]
  • Caregiver Support Group – September 9

    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 […]
  • Groupe de soutien en français – 9 septembre

    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 […]
  • Virtual Walk Meetup #1 – MEET & GREET

    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 the Week 1 Virtual Meet up. You will receive a confirmation email from Zoom with the link to join the event. FREE t-shirts will be […]
  • Walk for PF – Saskatoon

    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 […]
  • Clarke Walk for PF – Calgary

    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 […]
  • National Patient Support Group – September 17

    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 […]
  • Robert Davidson Walk for PF – Markham

    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 […]
  • Caregiver Support Group – September 23

    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 […]
  • Khan Family Walk for PF – Montreal

    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. […]
  • National Patient Support Group – October 1

    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 […]
  • Caregiver Support Group – October 7

    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. […]
  • Groupe de soutien en français – 7 octobre

    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, […]
  • National Patient Support Group – October 15

    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 […]
  • Caregiver Support Group – October 21

    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. […]
  • Caregiver Support Group – November 4

    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. […]
  • Groupe de soutien en français – 4 novembre

    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, […]
  • National Patient Support Group – November 5

    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 […]
  • Caregiver Support Group – November 18

    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. […]
  • National Patient Support Group – November 19

    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 […]
  • Caregiver Support Group – December 2

    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. […]
  • Groupe de soutien en français – 2 décembre

    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, […]
  • National Patient Support Group – December 3

    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 […]
  • Caregiver Support Group – December 16

    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. […]
  • National Patient Support Group – December 17

    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 […]
  • Newly Diagnosed Family Meetup

    Virtual Event
    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. 
  • Newly Diagnosed Family Meetup

    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 […]
  • Newly Diagnosed Family Meetup

    Virtual Event
    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. 
  • Newly Diagnosed Family Meetup

    Virtual Event
    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.