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Groupe de soutien national virtuel en français
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…
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Groupe de soutien national virtuel en français
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…
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Lighting of Prairie Winds Monument
On the evening of September 16, make sure to witness the Prairie Winds Monument of Saskatoon lit up in red and blue to recognize Global Pulmonary Fibrosis Awareness Month.
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Winnipeg Pulmonary Fibrosis Patient Education Forum (9am-2:30pm CT)
Join the annual Pulmonary Fibrosis Education Forum hosted by Manitoba Lung Association. This live event is open to patients and family affected by pulmonary fibrosis.
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Lighting of Montreal Olympic Park
On the evening of September 28, make sure to witness the Olympic Park of Montreal lit up in red and blue to highlight Global Pulmonary Fibrosis Awareness Month.
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Lighting of Edmonton High Level Bridge
On the evening of September 4, make sure to witness the High Level Bridge of Edmonton lit up in red and blue to recognize Global Pulmonary Fibrosis Awareness Month. The bridge will be lit up from 10 minutes before sunset until midnight.
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Khan Family Walk for PF – Montreal
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…
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Robert Davidson Walk for PF – Markham
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…
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Avonmore Berry Farm – Run the Farm (for PF)
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…
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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 someone in your life that you’d like to pay tribute to and can’t make an in-person event, this is the walk for you! FREE t-shirts…
