Our 6 month old daughter Sophia has CF,and so does our good friend Steve who also attends Lake Forest. Did you know there are quite a few families at Lake Forest that are also suffering from CF. CF is fairly rare. There are only 35,000 infants,children and adults that have CF in the US today. With funding the foundation has found new medication that has given most people with CF a median life expectancy of 37 years old. If you would like to help those with CF live a longer life and help the foundation find the CURE you can help by making a donation. If you would like to make a donation on behalf of Steve and Sophia you can make one online at http://cff.org click on find a walker enter my name Heather Freeman state NC then click on make a donation. Or you can mail a donation to
Cystic Fibrosis Foundation
Carolinas Chapter- Charlotte Office
7506 E. Independence Blvd Ste 120
Charlotte, NC 28226
Team Sophia's Strides
All the people with CF and their families really appreciate you helping fund the foundation to help FIND THE CURE FOR CF!!!!
God Bless,
The Freeman Family
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I'm so glad you posted this! Any of us with special needs in our families/lives need to speak up and raise awareness as much as possible. Thank you for sharing this with us!
MIchelle McConnell
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