We went to see Dr. Carey, the geneticist at Primary Children's Medical Center, this month. We weren't really sure what to expect at this appointment and were back and forth about going. We decided to go and came up with a list of questions about DiGeorge Syndrome. When we got there, they took a picture of Cole and a family picture. They did a physical evaluation and talked to us for about an hour. We didn't really learn anything new but we are hoping that they will be able to help us get Cole into speech therapy. He talks fairly well, but sometimes when he is really excited he is pretty hard to understand. The school district says he doesn't qualify for therapy and our insurance won't cover it because it is considered a developmental delay. We are going back down to SLC the first week of September to do a speech evaluation with a therapist who has seen a lot of DiGeorge kids. Dr. Carey will also put in his report that he would strongly recommend that Cole gets therapy through the school due to the majority of DiGeorge kids having speech issues. I hope that this will help us get somewhere. Dr. Carey also wants to have Cole's kidneys checked to make sure everything is going well with them. I guess that's something common in DiGeorge, too.
| Connor really liked that he could turn the water on with his feet but got frustrated because he wasn't tall enough to watch the water at the same time. |
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