Monday, November 2, 2009

Good report!!

I don't have a whole lot of time, but I just wanted to post about Caden's most recent trip to the cardiologist. At the beginning of each visit, she sits there with her hand on his heart. I'm not sure what she's feeling for, but she pushes down on his chest and then gets the stethoscope. She goes back forth between the hand and the stethoscope a few times, and then she looks in his ears and his mouth. She did comment on the great shape his teeth are in! :D Thanks to all that brushing. He brushes before nap time and again before bed. :)

When we got into the Echo room, he was a little leery. He had a small melt down in the first exam room, when he realized that he was at the Dr. :( He HATES going to the Dr. I can't say I blame him.

They did the EKG, and everything looked fine, the Dr. came in and started the echo, and Caden did great! :) He always does, but this time, he just watched the videos and every once in a while, he'd look at the Echo screen to see what she was doing. He was even holding her hand for a minute. Awwwwww lol

We (I mostly) always freak out when "it's taking too long". I realize that she's just being thorough, and who wouldn't want that?! It's so hard not to work yourself up though.

Turns out his numbers were slightly better than last time (AGAIN)! He just keeps getting better and better! His pressures are still very low through the conduit, and he seems to be handling his meds very well. She did say that the numbers may be better than last time because he may have been crying during the last echo. I don't remember him doing much crying that time, but it's still nice that his numbers continue to improve! :)

Because Caden is getting older, and he is not having huge growth spurts anymore, she decided that it would be okay for him to start going YEARLY!!! I about fainted. I have been waiting for the yearly visits for a long time now, and I still can't believe he's made it! :)

I really didn't care much for this particular Dr in the beginning, but the more we see her, the more friendly she becomes and the more we both begin to actually like her. She was the one that found the defect in the first place... well she performed his first echo anyway. I guess that makes me a little partial to her.

We are still on the same meds with the same doses. Have been on those doses for about a year and a half now. She said that by not upping the doses we are, in effect, weaning him off of them. Don't know how much longer he'll have to take them, she seemed a little hesitant to give a time frame.

All is well in Konecny land! :)

Cameron is doing well also. He's 10 months in less than a week! WOW that goes so fast. He is a super crawler! He'll get from one end of the house to the other in seconds! :) He's standing up on his own and starting to eat different kinds of foods. He'll be walking by Christmas, probably even Thanksgiving! :D I'll try to post pictures soon.

3 comments:

leasoup said...

This is great news for your little men!! Kiss their faces for me ;)

Eva's Mom said...

You made it! You made it! You made it! Yearly visits! YAY! That means...oh, that just means so many very very very very good things. I'm so happy for you!

Tanto said...

Your story is inspiring to all of us parents who have children with Truncus and more, keep up the great work Mom. My Isabel will be 9 Dec. 15th, and after 3 open hearts, and numerous other dealings, she is a totally normal little girl. We just had our checkup too at CHLA, and all was good. Take care. Morris Family