CF Foundation | How does cystic fibrosis affect the lungs?
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YouTubeCystic Fibrosis Foundation
CF Foundation | How does cystic fibrosis affect the lungs?
Cystic fibrosis is a genetic disease that affects multiple organs including the lungs. Watch this video to learn how non-CF lungs work and how CF affects the lungs over time. Learn more: https://www.cff.org/basics-lung-care
285.7K viewsMay 19, 2017
Cystic Fibrosis Foundation Cystic Fibrosis Awareness
6.4K views · 126 reactions | What does the future of CFTR modulators...
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6.4K views · 126 reactions | What does the future of CFTR modulators...
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Every day, the cystic fibrosis community achieves new milestones—from climbing up a flight of stairs, to graduating high school, growing families, and so much more. This CF Awareness Month, let's celebrate each and every achievement together. | Cystic Fibrosis Foundation
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Every day, the cystic fibrosis community achieves new milestones—from climbing up a flight of stairs, to graduating high school, growing families, and so much more. This CF Awareness Month, let's celebrate each and every achievement together. | Cystic Fibrosis Foundation
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122K views · 1.4K reactions | George M. Solomon, M.D., assistant...
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In honor of CF Awareness Month, singer-songwriter and musician Richard Marx has launched a new social media campaign and hashtag, #TakeaBreathforCF. Watch his video to learn how you can help us raise awareness for people living with cystic fibrosis and visit www.CFF.org/breath. | Cystic Fibrosis Foundation
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In honor of CF Awareness Month, singer-songwriter and musician Richard Marx has launched a new social media campaign and hashtag, #TakeaBreathforCF. Watch his video to learn how you can help us raise awareness for people living with cystic fibrosis and visit www.CFF.org/breath. | Cystic Fibrosis Foundation
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Cystic fibrosis is a family affair. From the moment of diagnosis, day-to-day expectations can transform for those with CF and everyone close to them. Virtually connect with the CF community about these experiences and more at our first-ever CF FamilyCon on Sunday, June 3! Check out the agenda and register today: http://on.cff.org/familycon | Cystic Fibrosis Foundation
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Cystic fibrosis is a family affair. From the moment of diagnosis, day-to-day expectations can transform for those with CF and everyone close to them. Virtually connect with the CF community about these experiences and more at our first-ever CF FamilyCon on Sunday, June 3! Check out the agenda and register today: http://on.cff.org/familycon | Cystic Fibrosis Foundation
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How have people with cystic fibrosis who have COVID-19 been doing? Our president and CEO, Mike Boyle, MD, provides an update of what we have learned. Have a question about CF and COVID-19? In this series experts from the CF Foundation and the CF care community will answer the top questions we are receiving. Submit your questions in the comments below. For more on CF and COVID-19: http://on.cff.org/COVID-19 | Cystic Fibrosis Foundation
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How have people with cystic fibrosis who have COVID-19 been doing? Our president and CEO, Mike Boyle, MD, provides an update of what we have learned. Have a question about CF and COVID-19? In this series experts from the CF Foundation and the CF care community will answer the top questions we are receiving. Submit your questions in the comments below. For more on CF and COVID-19: http://on.cff.org/COVID-19 | Cystic Fibrosis Foundation
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