Today was Cody's endo visit...our last one was in September. He had been doing really good and for a while I just thought this would be a routine visit. For the most part, it was but I had a couple issues to discuss with the doctor. Cody gets to the point and it's 8 o'clock and the kid needs to sleep. Which is fine but he seriously lately has been loosing his mind if he can't get to sleep. So I thought it was odd and night time has become a real chore with him. Crying, upset, can't sleep - I had no idea what to think or what was going on. A friend told me that his thyroid could be off. So today I told Dr. Wu about all the recent over tiredness and explained that not much has changed. If anything, his daily activity has gotten lighter with school being out. You can be more relaxed at home. Dr. Wu said that would explain his blood work. His TSH level is high. Last September it was 2.54 and today it was 5.5. He said that we need to increase his daily dose of medicine but because the range is high at 5.0 and Cody is just over that he is only increasing us a ½ a pill every other day. So every other day he will take 1 and ½ pills and 1 pill on the other day. Probably going to get confusing. He said that before the dose increase he was looking to take us off the med to see if his body had re-adjusted but because of the dose increase we are looking at another 1 to 2 years and then who knows. If we have to increase again then we are probably looking at something more long term. He wants to re-test the blood in 4 weeks and then he’ll let me know. He said he doesn’t need to see me unless those numbers come back really high or higher than we are at today. Right now we go back in Feb.
He said he is growing fine though. He weighed 60lbs and is in the 50th percentile for weight and height. So thankfully this thyroid issue is not affecting his growth. Which is good.
I explained it to Cody – I forget how big of a kid he really is when he has to be. I told him he has to have his blood taken again and he was OK with it. He had a good experience the other day when Brett took him. Matter of fact he just keeps reminding me that I promised him silly bands and haven’t gotten them yet. Although, he said he would take any “toy”, like a Bakugan! :) I just told him he was so tired and the pills help him not be as tired. And his body needs more of the pills so he won't be so tired. He said “I understand mom, I still love being me”. Yah, I could of cried!
So I knew something was up with my Cody. He has never had such a hard time falling asleep before. He’s been pretty attached at my hip lately too. And I have no idea why I let others make me feel like I don't know what I'm talking about or doing with him. I DO know him, I know him like the back of my hand. I've got this! We are a great team and even though Brett is there and has been very involved and great with Cody - Brett has always said he trust me 100% when it comes to things with Cody. So darn it, no more of that. If I feel like something is wrong - it is going to take a Doctor or more to prove to me that I am wrong!
Thursday, July 8, 2010
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