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  • National Patient Support Group – August 6

    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 – August 12

    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 […]
  • Avonmore Berry Farm – Run the Farm (for PF)

    Avonmore Berry Farm 16365 4 Rd, Avonmore, Ontario, Canada
    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 […]
  • National Support Group – August 20

    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 […]
  • Walk for PF – Winnipeg

    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 […]
  • Caregiver Support Group – August 26

    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. […]
  • 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 […]
  • 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 are walking. Registration is FREE 10:00 am CST | Check-in & children’s activities 10:45 am CST | Welcome message & opening stretch 11:00 pm CST […]
  • 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 for PF for this annual in-person walk for PF on September 14, 2024, from 10:30 am to 2 pm MDT. IN-PERSON WALK (10:30 am to […]
  • 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 motto “Never Surrender” be it negotiating the challenges of pulmonary fibrosis or just handling the challenges daily life brings to you.  Rather than give in […]
  • 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. “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 […]
  • 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 first and third Tuesdays of the month at 3 PM ET.  The topic for this session will be “Nutrition, Exercise, Pulmonary Rehabilitation & Introduction of […]
  • 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. The topic for this session will be “Nutrition, Exercise, Pulmonary Rehabilitation & Introduction of Book for Review”. You need to register in advance for this […]
  • 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, 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 […]
  • 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. 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 […]
  • 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. The topic for this session will be “Book for Review & Discussion”. You need to register in advance for this meeting in order to be […]
  • 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, 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 […]
  • 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 first and third Tuesdays of the month at 3 PM ET.  The topic for this session will be “Book for Review & Discussion”. You need […]
  • 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. 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 […]
  • 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 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 – 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. 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 […]
  • 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, 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 […]
  • 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 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 […]
  • 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. 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 […]
  • 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 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 […]
  • 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.