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Virtual Event
Walk Your Way for Pulmonary Fibrosis Can’t make it to an in-person walk? No problem! Join the CPFF Virtual Walk, Roll, Run and show your support—your way, in your own community, and with the people who matter most to you. Whether you’re walking solo, with family, or alongside a few close friends, every step helps raise […]
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Hello Nova Scotia PF community! We are excited to announce the second annual CPFF Hope Breathes Here Walk for pulmonary fibrosis in Yarmouth at 10:00AM ADT. You are invited to join the Campbells and many other PF supporters for a walk through Frost Park and along the historical waterfront. We’ll be walking rain or shine […]
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The Fab-5 invites you to join them as they walk for Helene and to raise awareness for pulmonary fibrosis. After our walk we will raise a toast to Helene at Michaelbrook Golf Course.
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Join us on September 13, 2025, for a meaningful day in the heart of the capital. Led by the Ottawa Patient Support Group, you are invited to join us in walking to honour loved ones, connect with others who understand, and raise awareness for pulmonary fibrosis in your own community. Let’s build community and take hopeful […]
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Members of the Ottawa CPFF Support Group welcome you to join in on a charity Pickleball Round Robin game, blending fun, fitness, and fundraising for a great cause. Ottawa pickleballers aim to raise awareness and support for the Canadian Pulmonary Fibrosis Foundation (CPFF), while building community and connection among those affected by the disease. With friendly competition […]
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The Clarke family invites you to gather with your community to walk for PF or cheer on those who are walking and enjoy a bbq afterwards.
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Join us for the 4th annual Robert Davidson Walk for PF, hosted by Heather Davidson. Bring the whole crew for a day of bonding, activities, and midday munchies at the local pub following our walk. Let’s unite, raise awareness, and make a difference for people living with pulmonary fibrosis. Join us on our walk, or […]
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The Niagara Falls will be lit up Red, Blue at 10:00pm for 15 minutes on September 20th to build awareness for pulmonary fibrosis
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CPFF is sponsoring the annual Patient Forum in Winnipeg hosted by Manitoba Lung Association. Attend virtually or in person to hear from healthcare experts and connect with others affected by pulmonary fibrosis.
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Support the Montreal Walk for PF The Khan family invites you to a community walk through the scenic trails of Angrignon Park, in Montreal, Quebec. — Encouragez la march pour la FP à Montréal La famille Khan vous invite à une marche communautaire à travers les sentiers pittoresques du Parc Angrignon, à Montréal, Québec. Enfilez vos […]
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The Canadian Pulmonary Fibrosis Foundation, the Robinson family, and fellow Islanders are proud to host the first CPFF Walk for Pulmonary Fibrosis on October 4, 2025 at 10:00 AM ADT, on the beautiful shores of PEI. Bring your friends, bring your family, and bring your big Island heart. Together, we’ll make every step count.
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