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sian newborns and less in other ethnic groups.
At this stage in Charlee's disease, due to the large amount of mucus her body creates her pancreas is no longer functioning. She now has to, and will always have to take enzymes prior to every meal she eats to do the work of the pancreas- aid in digestion. She also will have to undergo chest physical therapy multiple times a day for the rest of her life. This consists of percussion on her chest, side and back to loosen and break up mucus that damages and causes lung failure.
Charlee makes dealing with this disease as easy as possible. She is a beautiful, loving, happy baby. If she is not sleeping she is always happy and smiling, and making others do the same. You would never know looking at her of her diagnosis. Thanks to all of the support, fundraisers, donations and her amazing doctor team at children's hospital...we have HOPE. Thank you!
My Wish - Ms. Charlee Cook
The Adult Prom Flash Mob
Newscast of Adult Prom
Visit Claire's Place Foundation for the inspiration behind the flash mob!
Help us reach our goal of $20,000 in the fight against Cystic Fibrosis!