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 Watch Charlotte, whose son Trey has CF, talk about her dream for the future. 
 Watch Charlotte, whose son
 Trey has cystic fibrosis, talk
 about her dream for the future.
 

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My Dream

Video Series

Advances being made in CF research have the potential to make dreams come true for people with CF that were impossible just decades ago. The CF Foundation asked some of the many extraordinary people affected by this disease to share their dreams for the future. Caution: Contains sensitive and emotional dialogue from parents who have lost their children to CF.

Note: to embed these videos on your own personal website or blog, please visit the CF Foundation's YouTube Channel at www.youtube.com/CysticFibrosisUSA and click on the "My Dream" playlist.

 

 
 
 
 
 
 
 
 
 
 

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Updated 02/14/12

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The Cystic Fibrosis Foundation is an accredited charity of the Better Business Bureau.