Everyday Living With Idiopathic Pulmonary Fibrosis

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by Wendy Henderson |

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In this video from the Canadian Pulmonary Fibrosis Foundation shared in September 2014, we meet some patients and family members who are living with idiopathic pulmonary fibrosis. They talk about how the disease has impacted their lives, the symptoms they are dealing with and the choices they have had to face regarding lung transplants.

Discover 10 facts about lung transplants that you may not know. 

Idiopathic pulmonary fibrosis has no known cause and although it usually affects older people, it can affect children and young adults. Living with any chronic disease poses many challenges and frustrations along the way, and IPF is no exception. Our columnist, Charlene Marshall, talks about some of the things she finds most difficult about having IPF and how she is trying to adjust to her new life with the disease.

Find out more about  Hélène, a young woman who is waiting for a lung transplant to treat her IPF.

Pulmonary Fibrosis News is strictly a news and information website about the disease. It does not provide medical advice, diagnosis or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or another qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website.

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