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Jada ..

Our blog will update on Cystic Fibrosis...how it affects our family personally. Sometimes it is honest to the point of harshness. We live with CF everyday. Our 5 year old daughter, Zoe, has CF. Thank you for reading.....
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Long time since we updated!

Hello Family and Friends! We hope this finds you all doing well in 2015! So far, this has been a wonderful year for our family! Zoe has been...

Zoe is our HERO!!!

Zoe was admitted Wednesday after fighting a cough for a couple of months. She went in for her clinic sick follow up after being seen just 2 weeks...

Positive thoughts and prayers needed!

One of these days I'll be able to write good news in this blog! I'm positive it will happen! Zoe was re-admitted back into Wolfson...

Hospital again..... :-(

After 4 xrays over the last month....persistent coughing while Zoe is sleeping...she's sooooo tired. She went to her CF Dr on Friday. They...

June 2013

The CFF Great Strides walk was a success! There were many supporters for our little Zoe. Bonefish Grill brought their Zoe for Life...

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