Video Library
Patient & Caregiver Videos
CPFF Documentary – Breathless for Change
Many of us take breathing for granted. Although it may seem like an effortless …
The Khan Family’s Journey with Pulmonary Fibrosis
Wendy and Tina Khan’s father Jawaid was diagnosed with pulmonary fibrosis (PF), a fatal …
Le parcours de la famille Khan avec la FP
Jawaid, le père de Wendy et Tina Khan, a reçu un diagnostic de fibrose …
Finding Hope & Healing as a PF Caregiver – Sandi Bjorgum
Sandi Bjorgum was overcome with grief and shock when her father was first diagnosed …
Grieving What Was & Finding Acceptance for What Is – Heidi Schollengberg
Heidi Schollengberg is a pastor’s wife, a mother, grandmother, an oncology nurse, still working, …
A conversation about PF with Chris Sadleir
On July 23, 2016, Chris Sadleir’s father Rob who was living with pulmonary fibrosis …
Discussion sur la FP avec Chris Sadleir
Le 23 juillet 2016, Rob, le père de Chris Sadleir, qui vivait avec la …
Stan Hendriksen’s Journey with PF
Stan was diagnosed with Pulmonary Fibrosis (PF) in 2016, during a month-long hospitalisation for …
Le parcours de Stan Hendriksen avec la FP
Stan a reçu le diagnostic de fibrose pulmonaire (FP) en 2016, lors d’une hospitalisation …
The Clarke Family’s Journey with PF
Pulmonary fibrosis (PF) has played a devastating role in the lives of the Clarke …
Le parcours de la famille Clarke avec la FP
La fibrose pulmonaire (FP) a eu un effet dévastateur dans la vie de la …
A conversation about PF with Heather and Mark Davidson
CPFF founder Robert left a monumental legacy of awareness, information, and hope for the …
Discussion sur la FP avec Heather et Mark Davidson
Comme fondateur de la FCFP, Robert a légué un héritage monumental grâce à ses …
Talking about PF and Oxygen Featuring Todd Georgieff
Breathing is a fundamental human right. Home oxygen therapy is crucial for people living …
Discussion sur la FP et l’oxygène avec Todd Georgieff
Respirer est un droit humain fondamental. L’oxygénothérapie à domicile est essentielle pour les gens …
Donald Pamenter’s Pulmonary Fibrosis Journey
Nadine Fenton’s father Donald lived a very active and social life, and enjoyed playing …
Le parcours de Donald Pamenter avec la fibrose pulmonaire
Donald, le père de Nadine Fenton, avait une vie très active et un grand …
A conversation about pulmonary fibrosis featuring Angie Ortlieb
Angie Ortlieb’s dad Bruce was diagnosed with pulmonary fibrosis (PF) in 2011. Like many, …
Une conversation sur la fibrose pulmonaire avec Angie Ortlieb
En 2011, Bruce, le père d’Angie, a reçu un diagnostic de fibrose pulmonaire (FP) …
Patricia Meadows’ Pulmonary Fibrosis Journey
Patricia Meadows from Calgary, Alberta, lives with idiopathic pulmonary fibrosis (PF) with an underlying …
Le parcours de Patricia Meadows avec la fibrose pulmonaire
Patricia Meadows de Calgary, en Alberta, vit avec une fibrose pulmonaire idiopathique (FPI) et …
André Plouffe’s Pulmonary Fibrosis Journey
***UPDATE DEC 5, 2022: It is with great sadness that we announce the passing …
Le parcours d’André Plouffe avec la fibrose pulmonaire
André Plouffe de Sainte-Sophie, dans les Laurentides, au Québec vit avec un syndrome Mounier-Kuhn …
John Dennis’ Pulmonary Fibrosis Journey
“I’m relishing the fact that I can breathe,” declares John Dennis when he woke …
Le parcours de John Dennis avec la fibrose pulmonaire
« Je savoure le fait que je puisse respirer », déclare John Dennis lorsqu’il …
Jeannie Tom’s Pulmonary Fibrosis Journey
Jeannie Tom of Toronto, Ontario, lives with pulmonary hypertension and pulmonary fibrosis (PF) secondary …
Le parcours de Jeannie Tom avec la fibrose pulmonaire
Jeannie Tom de Toronto, en Ontario, vit avec une hypertension pulmonaire et une fibrose …
Rob Garbutt’s Pulmonary Fibrosis Journey
Rob Garbutt of Winnipeg, Manitoba, Canada lived with idiopathic pulmonary fibrosis (IPF) for a …
Le parcours de Rob Garbutt avec la fibrose pulmonaire
Rob Garbutt de Winnipeg, au Manitoba, au Canada vit avec la fibrose pulmonaire idiopathique …
Naomi Matsushita’s Pulmonary Fibrosis Journey
Naomi Matsushita of Toronto, Ontario, Canada, has interstitial pneumonia, one of the 200 types …
Le parcours de Naomi Matsushita avec la fibrose pulmonaire
Naomi Matsushita de Toronto, Ontario, Canada, souffre d’une pneumonie interstitielle, l’un des 200 types …
Educational Videos
Tackle the Crackle – Know the Signs of Pulmonary Fibrosis
Tackle the Crackle! Know the signs of pulmonary fibrosis. Early pulmonary fibrosis detection is …
So You’ve Been Diagnosed with Pulmonary Fibrosis…What’s Next? – Dr. Charlene Fell
If you or someone you care about is living with pulmonary fibrosis this is …
J’ai reçu un diagnostic de fibrose pulmonaire… que faire maintenant? – avec Dr Ilan Azuelos
Si une personne chère ou vous-même vivez avec la fibrose pulmonaire, regardez attentivement cette …
Community Events
Clarke Walk for Pulmonary Fibrosis – Calgary (Event Coverage by CityNews)
Thousands of Canadians live with Pulmonary Fibrosis (PF). Danina Falkenberg from CityNews learns about …
Greetings from Hon. Audrey Gordon – Manitoba Minister of Health
Honourable Audrey Gordon brings greetings on behalf of the province of Manitoba in recognition …
PF Month Greetings from Hon. Paul Merriman, Saskatchewan Minister of Health
Saskatchewan Minister of Health, Hon. Paul Merriman sends his greetings for Pulmonary Fibrosis month …
CPFF 2022 Pulmonary Fibrosis Month Highlight Reel
Watch the CPFF 2022 PF Month Highlight reel to see how PF Month was …
Pulmonary Fibrosis Month Greetings from Manitoba Premier Heather Stefanson
Heather Stefanson, Premier of Manitoba stands with CPFF as we work to support people …
Greetings from Hon. Tom Osborne – Minister of Health for Newfoundland and Labrador
Honorable Tom Osborne, Minister of Health and Community Services for Newfoundland and Labrador, acknowledges …
Greetings from Ontario Premier Doug Ford for PF Month
Ontario Premier Doug Ford sends his greetings to Canadians for 2022 global pulmonary fibrosis …
Pucker Up Challenge
Pucker Up Around the World for PF
People around the world are puckering up for pulmonary fibrosis. See what it feels …
Take the CPFF Pucker Up Challenge!
This year the Canadian Pulmonary Fibrosis Foundation is challenging Canadians from coast to coast …
Relevez le défi Qu’une paille pour respirer
Cette année, la Fondation canadienne de la fibrose pulmonaire met au défi les Canadiens …
Jamp Pharma Took the Pucker Up Challenge
Jamp Pharma took the CPFF Pucker Up Challenge to experience what it’s like to …
AFIPIA Brazil Takes the Pucker Up Challenge
APIFIA is encouraging Brazil to take the CPFF Pucker Up Challenge to help raise …
AFIPIA Spain Takes the Pucker Up Challenge
APIFIA encourages Spain to help raise awareness and show support for those living with …
Acepte el Desafío de fruncir los labios
La mayoría de nosotros damos por sentada la respiración. Pero, para las personas con …
العنوان: شاركوا في تحدي ضم الشفاه للتنفس
شاق. وصف البعض الأمر بمحاولة المرء التنفس من خلال شفاطة بينما يكون مربوطًا بجهاز …
Aceite o desafio para franzir os lábios
A maioria de nós considera a respiração algo natural. Mas, para pessoas com uma …
接受“抿嘴呼吸Pucker Up”挑战
我们大多数人都认为呼吸是理所当然的。 但是，对于患有肺纤维化等肺部疾病的人来说，呼吸是一项艰巨的任务。 有人描述全天候被拴在氧气机上的感受，就像试图通过吸管呼吸。 …
Clarke Walk for Pulmonary Fibrosis – Calgary (Event Coverage by CityNews)
Thousands of Canadians live with Pulmonary Fibrosis (PF). Danina Falkenberg from CityNews learns about …
Greetings from Hon. Audrey Gordon – Manitoba Minister of Health
Honourable Audrey Gordon brings greetings on behalf of the province of Manitoba in recognition …
Boehringer Ingelheim Global takes the CPFF Pucker Up Challenge
Have you ever wondered what it’s like to have chronically short breath? For those …
Boehringer Ingelheim Canada took the CPFF Pucker Up Challenge
Boehringer Ingelheim Canada took the CPFF Pucker Up Challenge to experience how it feels …
