On July 13, 2015 our family was blessed with a beautiful boy – 10 fingers, 10 toes. Three days later as Caleb was preparing to leave the hospital and move home to join his big sister, he was admitted to the NICU. The routine infant screening results told a story that rocked our world and changed our lives forever. Caleb was diagnosed with a rare genetic disorder called Di George Syndrome. The diso
rder presented countless issues that our family needed to understand and learn how to deal with but the most monumental challenge was that Caleb would need a G-tube for survival. That became a full time job – hooking up and disconnecting the tube every hour, 24 hours a day, 7 days a week. It was exhausting for us as caretakers, but it took a toll on Caleb as we had to undress him every time, interrupting his much-needed sleep. We desperately sought out a solution that would allow for minimal disruption during the G-tube changing routine. It’s been said you should never wake a sleeping baby, and while that might only partially be true, there must be a rule somewhere that says you shouldn’t wake them every hour. Caleb’s health and growth depended on our finding a way to access the port without un******ng him. Caleb is not unique in his G-tube needs. Thousands of children worldwide have similar disorders, leaving caretakers with the same challenges ours has faced. We are pleased to launch C.C. Moo LLC, a stylish and discrete adaptive clothing line. Moo LLC is focused on providing ease and convenience to all families who desire a unique way to minimize the hassle of accessing tubes for feedings or treatments. “Stylish and discrete adaptive clothing, changing the quality of children’s lives one ZIP & SNAP at a time”
