It has been quite a while since I last updated here.I believe the last update was in September. Since then, we found, bought and moved into our new house! We found a 3 bedroom 2 bath house that was perfect for our family! When we first saw the house it was naked. Litterally! It was in the middle of a complete renovation! There was no paint, no flooring, no cabinets and no windows! I'm going ot try a new way of sharing photos with you. Here are pictures of our naked house and pictures of it finished.
Nathan is growing like a weed. He is scooting along now and saying mamma and dadda. He is the happiest little boy ever! He had an appointment with his pediatrician for his routine 9 month appointment. He weighed in at 19 pounds and 27 inches long! She asked me if there was anything I was concerned about or had any questions. I asked her again about the ridge that he has down the middle of his skull still. At a previous appointment we had discussed this and the pediatrician decided we would "watch it" and that he would "grow out of it". She looked at his head, felt his ridge and asked me if his head looked funny to me. I told her it wasn't round and that his temple are sunken in. That's when everything changed. She decided she wanted to get a CT scan done on his head and see what she could see and the nurse would call me to let me know when the appointment at the hospital was. I left that appointment more confused and worried than ever. It was just me and the kids and I drove home as quickly as possible becasue I knew I had to do some research. The kids went off to nap time and I went off to my computer. After hours of reading I found out what should have been diagnosed 9 months ago.Our appointment was set for Tuesday, December 1st. While the week slowly passed, we celebrated Thanksgiving twice and had a blast but the whole time all I could think about was what might be and the CT scan ahead. The night before we had to fast Nathan since he was being sedated. I wasn't sure how well he would do with not eating. I woke him up at 3:45am for his last bottle until noon the next day. Finally Tuesday arrived. My aunt came over to watch Brian since children under 18 who aren't patients aren't allowed at the Children's Hospital becasue of H1N1. We got there at 9:30. We were taken back to the CT area so that they could sedate Nathan. The scan they were doing is a 3D reconstructive scan. It requires them to be completly still. They tried 3 times to get the IV in him and kept missing.
I called the pediatricians office that afternoon and was told they would call me first thing in the morning. Around 9:15 the phone rang! Of course it rang about 4 times before that and every time I nearly jumped out of my skin every time. But THE call came. The pediatrician called and said that Nathan had Craniosynostosis. It is just what I thought he had. What is that you might be wondering.
What is Craniosynostosis? In an infant, the skull is not a solid piece of bone, but several boney plates separated by fibrous sutures. These sutures allow room for growth as an infant develops, and will eventually fuse to form a solid skull. Craniosynostosis is a condition in which one or more of these sutures fuse prematurely, causing restricted skull and brain growth. The result is an abnormally shaped head, or in severe cases, increased pressure on the brain. It is often sporadic with unknown cause, but can sometimes be linked a genetic syndrome. A physician’s examination as well as X-rays and/or a CT scan are required in order to properly diagnose craniosynostosis.
Oh and while all of this has happened, this weekend Dean has been sick, Brian got strep throat, and Nathan popped a 102 fever.Everyone is well now except Dean. I'll write more tomorrow. BYE!