Video Library

Patient & Caregiver Videos

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CPFF Documentary – Breathless for Change

Many of us take breathing for granted. Although it may seem like an effortless …
Roy Alderice’s Journey with Pulmonary Fibrosis

Roy Alderice’s Journey with Pulmonary Fibrosis

Jennifer and Bill Clements recount the journey of Jennifer’s late father, Roy Alderice, from …
Karen Wade’s Journey with Pulmonary Fibrosis

Karen Wade’s Journey with Pulmonary Fibrosis

Karen’s pulmonary fibrosis (PF) journey began with a recurring cough, and being an avid …
Woman standing in park with 2 grandchildren

Le parcours de Karen Wade avec la fibrose pulmonaire

Le parcours de Karen avec la fibrose pulmonaire (FP) a commencé par une toux …
The Phillips Family's Journey with Pulmonary Fibrosis

The Phillips Family’s Journey with Pulmonary Fibrosis

The Phillips family has been profoundly affected by pulmonary fibrosis (PF), a disease that …
Le parcours de la famille Phillips avec la fibrose pulmonaire

Le parcours de la famille Phillips avec la fibrose pulmonaire

La famille Phillips a été profondément affectée par la fibrose pulmonaire (FP), une maladie …
The Schuler Family's Journey with Pulmonary Fibrosis

The Schuler Family’s Journey with Pulmonary Fibrosis

Hans Schuler’s journey with pulmonary fibrosis (PF) began when a bout of winter pneumonia …
Le parcours de la famille Schuler avec la fibrose pulmonaire

Le parcours de la famille Schuler avec la fibrose pulmonaire

Le parcours de Hans Schuler avec la fibrose pulmonaire (FP) a commencé lorsqu’il a …
Two sisters in park looking at each other

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

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

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

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

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

Discussion sur la FP avec Chris Sadleir

Le 23 juillet 2016, Rob, le père de Chris Sadleir, qui vivait avec la …
Man with text: "BREATHLESS for CHANGE: LIVING WITH PULMONARY FIBROSIS featuring Stan Hendriksen"

Stan Hendriksen’s Journey with PF

Stan was diagnosed with Pulmonary Fibrosis (PF) in 2016, during a month-long hospitalisation for …
Man with text: "À BOUT DE SOUFFLE pour du CHANGEMENT: VIVRE AVEC LA FIBROSE PULMONAIRE avec Stan Hendriksen"

Le parcours de Stan Hendriksen avec la FP

Stan a reçu le diagnostic de fibrose pulmonaire (FP) en 2016, lors d’une hospitalisation …
Girl, boy, and woman with text: "BREATHLESS for CHANGE: A CONVERSATION ABOUT PULMONARY FIBROSIS featuring Jackie Clarke, Abbie Clarke, and Rayyan Aldosary"

The Clarke Family’s Journey with PF

Pulmonary fibrosis (PF) has played a devastating role in the lives of the Clarke …
Boy, girl, and woman with text: "À BOUT DE SOUFFLE pour du CHANGEMENT: UNE CONVERSATION SUR LA FIBROSE PULMONAIR avec Jackie Clarke, Abbie Clarke et Rayyan Aldosary"

Le parcours de la famille Clarke avec la FP

La fibrose pulmonaire (FP) a eu un effet dévastateur dans la vie de la …
Man and woman with text: "BREATHLESS for CHANGE: A CONVERSATION ABOUT PULMONARY FIBROSIS featuring Heather and Mark Davidson"

A conversation about PF with Heather and Mark Davidson

CPFF founder Robert left a monumental legacy of awareness, information, and hope for the …
Man and woman with text: "À BOUT DE SOUFFLE pour du CHANGEMENT: UNE CONVERSATION SUR LA FIBROSE PULMONAIR avec Heather et Mark Davidson"

Discussion sur la FP avec Heather et Mark Davidson

Comme fondateur de la FCFP, Robert a légué un héritage monumental grâce à ses …
Man among trees with text: "BREATHLESS for CHANGE: A CONVERSATION ABOUT PULMONARY FIBROSIS featuring Todd Georgieff"

Talking about PF and Oxygen Featuring Todd Georgieff

Breathing is a fundamental human right. Home oxygen therapy is crucial for people living …
Man among trees with text: "À BOUT DE SOUFFLE pour du CHANGEMENT: UNE CONVERSATION SUR LA FIBROSE PULMONAIR avec Todd Georgieff"

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 …
A man holding a cat with text: "BREATHLESS for CHANGE: A CONVERSATION ABOUT PULMONARY FIBROSIS a tribute to Donald Pamenter"

Donald Pamenter’s Pulmonary Fibrosis Journey

Nadine Fenton’s father Donald lived a very active and social life, and enjoyed playing …
Man holding cat with text: "À BOUT DE SOUFFLE pour du CHANGEMENT: UNE CONVERSATION SUR LA FIBROSE PULMONAIR en hommage à Donald Pamenter"

Le parcours de Donald Pamenter avec la fibrose pulmonaire

Donald, le père de Nadine Fenton, avait une vie très active et un grand …
Breathless for Change featuring Angie Ortlieb

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

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’ Pulmonary Fibrosis Journey

Patricia Meadows from Calgary, Alberta, lives with idiopathic pulmonary fibrosis (PF) with an underlying …
Patricia Meadows FR

Le parcours de Patricia Meadows avec la fibrose pulmonaire

Patricia Meadows de Calgary, en Alberta, vit avec une fibrose pulmonaire idiopathique (FPI) et …
Le parcours d’André Plouffe avec la fibrose pulmonaire

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

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 …
Breathless for Change Video featuring John Dennis

John Dennis’ Pulmonary Fibrosis Journey

“I’m relishing the fact that I can breathe,” declares John Dennis when he woke …
John Dennis

Le parcours de John Dennis avec la fibrose pulmonaire

« Je savoure le fait que je puisse respirer », déclare John Dennis lorsqu’il …
Jeannie Tom Breathless for change

Jeannie Tom’s Pulmonary Fibrosis Journey

Jeannie Tom of Toronto, Ontario, lives with pulmonary hypertension and pulmonary fibrosis (PF) secondary …
jeannie tom

Le parcours de Jeannie Tom avec la fibrose pulmonaire

Jeannie Tom de Toronto, en Ontario, vit avec une hypertension pulmonaire et une fibrose …
Man with oxygen and his dog

Rob Garbutt’s Pulmonary Fibrosis Journey

Rob Garbutt of Winnipeg, Manitoba, Canada lived with idiopathic pulmonary fibrosis (IPF) for a …
Rob Garbutt

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 Breathless for Change

Naomi Matsushita’s Pulmonary Fibrosis Journey

Naomi Matsushita of Toronto, Ontario, Canada, has interstitial pneumonia, one of the 200 types …
Naomi Matsushita

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

COVID-19 et fibrose pulmonaire : connaître les signes de la FP - Farrell Eckman

COVID-19 et fibrose pulmonaire : connaître les signes de la FP – Farrell Eckman

La vie de Farrell Eckman a été transformée à jamais lorsqu’elle a attrapé la …
COVID-19 & Pulmonary Fibrosis: Know the Signs of PF - Farrell Eckman

COVID-19 & Pulmonary Fibrosis: Know the Signs of PF – Farrell Eckman

Farrell Eckman’s life was forever changed when she caught COVID-19; the damage sustained to …
Pulmonary Fibrosis Symptoms: Listen for the Signs

Pulmonary Fibrosis Symptoms: Listen for the Signs

Pulmonary fibrosis (PF) is a rare disease, so it is not often top of …
Doctor listening with a stethoscope

Symptômes de la fibrose pulmonaire : écoutez les signes

La fibrose pulmonaire (FP) est une maladie rare; donc, on n’y pense pas immédiatement …
Lungs behind a title Tackle the Crackle

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

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 …
Whiteboard video blog post

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

Woman pointing to herself with copy that says shine your light

Shine your light on pulmonary fibrosis

Our communities across Canada are shining their light on #pulmonaryfibrosis and the people living …
Shine your light on pulmonary fibrosis

Shine your light on pulmonary fibrosis

The Canadian Pulmonary Fibrosis Foundation is uniting Canadians once again to shine a light …
Clarke Walk for Pulmonary Fibrosis - Calgary (Event Coverage by CityNews)

Clarke Walk for Pulmonary Fibrosis – Calgary (Event Coverage by CityNews)

Thousands of Canadians live with Pulmonary Fibrosis (PF). Danina Falkenberg from CityNews learns about …
Honourable Audrey Gordon speaks in front of a Manitoban tapestry

Greetings from Hon. Audrey Gordon – Manitoba Minister of Health

Honourable Audrey Gordon brings greetings on behalf of the province of Manitoba in recognition …
Saskatchewan Minister of Health Paul Merriman

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 …
Family gathering for PF month.

CPFF 2022 Pulmonary Fibrosis Month Highlight Reel

Watch the CPFF 2022 PF Month Highlight reel to see how PF Month was …
Manitoba Premier Heather Stefanson

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

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 …
Ontario Premier Doug Ford

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

Get Moving with the CPFF Pucker Up Challenge

Get Moving with the CPFF Pucker Up Challenge

Imagine walking a few blocks around your neighbourhood while pulling a loaded suitcase and …
Pucker Up Around the World for PF

Pucker Up Around the World for PF

People around the world are puckering up for pulmonary fibrosis. See what it feels …
Woman breathing through a straw

Take the CPFF Pucker Up Challenge!

This year the Canadian Pulmonary Fibrosis Foundation is challenging Canadians from coast to coast …
Woman breathing through a straw

Relevez le défi Qu’une paille pour respirer

Cette année, la Fondation canadienne de la fibrose pulmonaire met au défi les Canadiens …
Avonmore takes the Pucker Up Challenge

Avonmore takes the Pucker Up Challenge

Many thanks Avonmore, Ontario for Puckering Up for pulmonary fibrosis. Try the Pucker Up …
Calgary takes the Pucker Up Challenge

Calgary takes the Pucker Up Challenge

Thank you to Calgary, Alberta for taking the Pucker Up Challenge for pulmonary fibrosis …
Montréal takes the Pucker Up Challenge

Montréal takes the Pucker Up Challenge

Try the Pucker Up Challenge yourself to see how eye-opening it is. Let’s unite …
Markham takes the Pucker Up Challenge

Markham takes the Pucker Up Challenge

Thanks Markham, Ontario for puckering up for pulmonary fibrosis (PF). Try the Pucker Up …
Five people block their noses while breathing through straws.

Jamp Pharma Took the Pucker Up Challenge

Jamp Pharma took the CPFF Pucker Up Challenge to experience what it’s like to …
Portuguese text on a white background reading "help us raise awareness about idiopathic pulmonary fibrosis".

AFIPIA Brazil Takes the Pucker Up Challenge

APIFIA is encouraging Brazil to take the CPFF Pucker Up Challenge to help raise …
Spanish text on white background reading "Help us raise awareness about Idiopathic Pulmonary Fibrosis!".

AFIPIA Spain Takes the Pucker Up Challenge

APIFIA encourages Spain to help raise awareness and show support for those living with …
Two women holding straws and cell phones

Acepte el Desafío de fruncir los labios

La mayoría de nosotros damos por sentada la respiración. Pero, para las personas con …
Three happy men posing for photo

العنوان: شاركوا في تحدي ضم الشفاه للتنفس

شاق. وصف البعض الأمر بمحاولة المرء التنفس من خلال شفاطة بينما يكون مربوطًا بجهاز …
Two women blowing air through straws

Aceite o desafio para franzir os lábios

A maioria de nós considera a respiração algo natural. Mas, para pessoas com uma …
Woman breathing through a straw

タイトル: 口すぼめ呼吸チャレンジに挑戦

私たちの多くは呼吸を当たり前のように行っています。 しかし、肺線維症のような肺疾患をもつ患者さんにとって、呼吸は「重労働」なのです。 …
Lady breathing through straw

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。 …
Woman pointing to herself with copy that says shine your light

Shine your light on pulmonary fibrosis

Our communities across Canada are shining their light on #pulmonaryfibrosis and the people living …
Shine your light on pulmonary fibrosis

Shine your light on pulmonary fibrosis

The Canadian Pulmonary Fibrosis Foundation is uniting Canadians once again to shine a light …
Clarke Walk for Pulmonary Fibrosis - Calgary (Event Coverage by CityNews)

Clarke Walk for Pulmonary Fibrosis – Calgary (Event Coverage by CityNews)

Thousands of Canadians live with Pulmonary Fibrosis (PF). Danina Falkenberg from CityNews learns about …
Honourable Audrey Gordon speaks in front of a Manitoban tapestry

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

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

Boehringer Ingelheim Canada took the CPFF Pucker Up Challenge to experience how it feels …

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