Young Mom Needs Double Lung Transplant -- Grace White

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A young mom with a rare disease is fighting for her life. Tonight, she's at University Hospital on the waiting list for a double lung transplant. Her family is sharing her story, hoping to save her life and many others. "She is a beautiful woman. The most beautiful woman I know," said Alissa ...

Somebody That I Used To Know by Goyte-Cover by Abby Rose & Mason

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Abby Rose & Mason are performing at a Cystic Fibrosis Fundraiser at Indigo Bookstore. Abby Rose, Charlie & Mason raised a total of $805 that evening to help find a cure for this disease. Abby & Charlie's cousins have Cystic Fibrosis and we hope to find a cure one day soon! Thx for watching and for ...

Patron handles disease, volleyball with care

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(Boston Globe) Chelmsford boys volleyball player Zach Patron manages his cystic fibrosis while leading his team. (Video by Liz Torres, Globe Correspondent)

The Real Deal ( Cystic Fibrosis Documentary 22)

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Hot Dog Safari

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The Phantom Gourmet Hot Dog Safari is an entire day of food and fun for the whole family. The best part? It's all to benefit the Joey Fund and Cystic Fibrosis.

DJ Spoony

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The Nicky's Whisper Challenge Trophy 2012 This is a an annual match played in memory of Nicky West, who had Cystic Fibrosis and was a remarkable woman and tireless ambassador for the Cystic Fibrosis Trust. Her repeated determination and spirit were an inspiration to us all.

Dalton Grant

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The Nicky's Whisper Challenge Trophy 2012 This is a an annual match played in memory of Nicky West, who had Cystic Fibrosis and was a remarkable woman and tireless ambassador for the Cystic Fibrosis Trust. Her repeated determination and spirit were an inspiration to us all.

Chris Wolstenholme

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The Nicky's Whisper Challenge Trophy 2012 This is a an annual match played in memory of Nicky West, who had Cystic Fibrosis and was a remarkable woman and tireless ambassador for the Cystic Fibrosis Trust. Her repeated determination and spirit were an inspiration to us all.

Inspirational 7yo living with cystic fibrosis

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A brave seven-year-old Cranbourne girl is providing an inspiration for the three thousand other Australians living with cystic fibrosis.

Nevermind - Day 5 & 6 VLOG [23.5.2012] & [24.5.2012]

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Haha how can i say 'i don't know what to talk about'???i was going on for ages? O_o anyway... p;~ Please Read ~ Right. It was kind of awkward recording in the hospital so i apologize for that and kind of talking about random stuff hehe. I'm going to explain on here, if i can, a bit more simply. So, ...