Pep Talk for Kids with Cystic Fibrosis

In this The Frey Life video, here’s Mary talking about her cystic fibrosis experience directly to kids going through the same.

“If you’re a kid with cystic fibrosis or are a parent of a CF kid, Mary wants to encourage you to keep doing your best to care for your body!”

To learn more about cystic fibrosis, click here: http://bit.ly/1QltnFs

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Cystic Fibrosis News Today 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 other 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.

3 comments

  1. Amanda Denahan says:

    My nine year old daughter, Sage, would like to answer Mary’s questions…Her favorite color is teal. My parents remind me to take my medicine still, except for enzymes. At school, I keep my enzymes in my lunchbox. Yes, I have a vest, but mine is blue, green, yellow and pink, with flowers on it – it’s called “flower power!” Thank you very much for the pep talk! 🙂

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