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James and his Bard Button

After more than 21/2 years, James underwent another procedure to replace his G-tube with a Bard button. No more long tube! (Big sigh of relief). 

Contents of a Bard kit 
Prepped for the procedure
Monitor for vital signs
The Bard looks like a flat thingy on top of his tummy with a kind of flip-to-open cover. It has connecting tubes that we use for feeding.

Hello, Bard!
Still groggy from the anesthesia

Can we go home now?


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About This Blog

Hi everyone! This site is created to chronicle the life of Gideon James Floresca , born a preemie on September 18, 1997. He has been diagnosed with global psychomotor delay and has the spastic quadriplegic type of cerebral palsy .  Look how small James was when he was born!  He has been "eating" via a feeding tube since he was five due to failure to thrive. From an NGT (naso-gastric tube) that we used for more than 3 years, he underwent surgery in 2005 so a gastrostomy tube can be placed directly in his tummy. In March 2008, we were able to afford a Bard button which made feeding him so much easier. He's currently 100% tube-fed with complete food formula. James at 4 months old It is our hope that his story will serve to inspire and encourage even families with "normal" children. Join us in our continuous journey of hope :)