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Kelli
On Blogger since: July 2010
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IntroductionHey everyone! My name is Kelli, and I am Kannon's mom. Thank you for taking the time to visit and feel free to leave comments or prayers for our sweet baby boy. As for his story, it began when we had our follow up appointment after my first ultrasound. We were told then that there was a chance he had echogenic fetal bowel (which they later ruled out). From that point they decided I was "high risk" and had me visit a specialist every month. After months of hearing Dr's tell me what they thought, FINALLY Kannon had arrived! He was born on April 1, 2010. Little did the Dr's know, that the joke was on them. He was perfect--in every way that I had imagined he would be. After he was born, he made the NICU his home for the next 11 days. During that time Dr's had several tests ran (ultrasounds, MRI’s, Genetics). Finally, the Dr's came back with results. He has partial agenesis of the corpus callosum (p-ACC). After finding this out they began genetic testing, and found he had an extra chromosome. After undergoing a more in depth test called FISH, we were told Kannon has Tetrasomy i(5p) Mosaicism. There are only 3 other clinical reports in the world, and Kannon is number 4.
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