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their daughter’s skull did not fuse completely and therefore had left an opening in her lip and possibly another in the roof of her mouth. Missy still gets choked up thinking about that day, “It was not easy for me to comprehend how dicult Mia’s life was going to be and I needed my own time to process the news and deal with it in my own way.” But the Lord giveth and the Lord taketh away and what Missy and Jase Robertson did not realize at the time, was that the Lord was giving them a daughter who would help take fear away from other children. It was truly a blessing that Mia was diagnosed before being born because it gave Jase and Missy an adequate amount of time to prepare their family and nd the best physicians to help Mia soon after she arrived. “The sooner a child with cleft lip or cleft palete is treated, the better,” Missy explains, “and we were sitting in Dallas at the International Craniofacial Institute when Mia was only seventeen days old.” She was tted with an appliance that created a fake roof in her mouth so that she would be able to eat well and gain as much weight as possible in preparation for her rst surgery. At three months, Mia’s team of doctors performed corrective surgery on her cleft lip. “We were in no way prepared for what was coming post-surgery.” Missy is not referring to taking care of Mia or her recovery, but how dierent the baby girl she and Jase had fallen in love with looked with the stitches and swelling after coming out of surgery. “I wondered if we’d made the right choice and I was really emotionally upset, afraid that this had been the wrong decision because it was supposed to make her better.” It didn’t take long for Missy to realize that their decision was indeed made in the best interest of their daughter, as the swelling went down and Mia recovered quickly and made great strides in preparation for her next surgery that would take place in four short months. “I want to help other parents be more prepared for what they will see post-surgery. I understand now that the swelling and stitches and pain are temporary, but I wasn’t ready that day and it was so scary.” This is one of the many reasons that Missy and Jase are working diligently to raise awareness about conditions like Mia’s; they don’t want other parents to go through any more trauma than necessary by questioning their decisions because they aren’t ready for the difference in their baby after the surgery. As a mother, I can’t begin to imagine walking a mile in their shoes or
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