Thanks to my friend,
Nate, who posted this on his blog- I thought i'd continue to spread the word about a new documentary film coming out about Cystic Fibrosis. It's about a girl named Eva, telling her story about living with Cystic Fibrosis

and the process of a lung transplant. The film hasn't been released yet, but I posted the link for the trailer below. Can't wait to see it, I am a fan of people's stories being told! Let's get the word out about CF and this awesome story.
~Em
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