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CPFF Documentary – Breathless for Change
This documentary explores the courage and resilience of people living with PF and uncovers the barriers to accessing equitable healthcare for treatment and disease management.
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CPFF Documentary – Breathless for Change
Many of us take breathing for granted. Although it may seem like an effortless act, for people with a rare disease like pulmonary fibrosis (PF), breathing can be a painful […]
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A unique case sparks a passion for ILD research and patient care
“My interest in ILD began during my respirology elective, when I cared for a 30-year-old man with PPFE (Pleuro Parenchymal Fibro Elastosis, a rare ILD).” This is how Dr. Bohyung […]
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Shortness of Breath
Living a healthy life changed totally in one day. On Tuesday, July 12, 2022, I was repairing a tile floor in our back balcony. Suddenly, I was out of breath […]
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A conversation about pulmonary fibrosis featuring Angie Ortlieb
Angie Ortlieb’s dad Bruce was diagnosed with pulmonary fibrosis (PF) in 2011. Like many, they had never heard about this disease before. Bruce was a hard worker and a proud […]
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Acepte el Desafío de fruncir los labios
La mayoría de nosotros damos por sentada la respiración. Pero, para las personas con una enfermedad pulmonar como la fibrosis pulmonar, respirar es un TRABAJO DIFÍCIL. Algunos lo han descrito […]
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العنوان: شاركوا في تحدي ضم الشفاه للتنفس
شاق. وصف البعض الأمر بمحاولة المرء التنفس من خلال شفاطة بينما يكون مربوطًا بجهاز أكسجين على مدار الساعة طوال أيام
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Aceite o desafio para franzir os lábios
A maioria de nós considera a respiração algo natural. Mas, para pessoas com uma doença pulmonar como a fibrose pulmonar, respirar é um TRABALHO DIFÍCIL. Alguns descreveram isso como uma […]
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Alberta 2023 Election Advocacy Toolkit
The Alberta general election will be held on May 29, 2023. The campaign period commenced on May 1, 2023 and will last 28 days. This election provides an opportunity for […]
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Une conversation sur la fibrose pulmonaire avec Angie Ortlieb
En 2011, Bruce, le père d’Angie, a reçu un diagnostic de fibrose pulmonaire (FP). Comme pour bien d’autres personnes, sa famille et lui n’avaient jamais entendu parler de cette maladie […]
