TYSON MATTHEW KOTTELENBERG

This blog is about our 14 year old son Tyson. Tyson was born with serious complex congenital heart defects, (Hypoplastic Right Ventricle, Tricuspid Atresia, Coarctation of Aorta, Transposed Great Arteries, with VSD and ASD.) In short, the right side of his heart is completely under-developed (he has half a heart,) his main arteries are mixed up, and his aorta is narrow. He has undergone 3 open-heart surgeries and 5 heart catheterization procedures to try to 'repair' his heart. Tyson also has severe narrowing in his pulmonary veins which are causing higher venous pressures. He's still doing AMAZINGLY well all things considered. We entrust our dear son into the hands of God, knowing that in all things God works for the good of those who love Him!

HAPPY FIRST BIRTHDAY TY!


On Saturday, November 21, 2009, Tyson celebrated his first birthday with family and friends. We hosted a come-and-go birthday party in the basement of the church. Here are some highlights.

Oh, and by the way, Tyson is crawling! Yay! He started on Wednesday just before his birthday, and he is now off to the races! You should have seen how fast he could crawl when he was going for the hockey sticks! I have finally admitted that the love for hockey is not a learned thing, but it really is born in them. I think it comes with the last name "Kottelenberg." *sigh* I guess there's just nothing I can do about it. I might as well just give up. LOL




















DIG IN!
Tyson sure got spoiled!
Playing with his gifts at home.

Wednesday, November 11, 2009

Tyson had his routine clinic appointment at Sick Kids today. He didn't need an echocardiogram this time but just an ecg. (Echocardiogram is an ultrasound of the heart - a test that uses sound waves to create a moving picture of the heart. An ecg records electrical activity of the heart on a graph.) Tyson had nothing invasive done today or anything involving sedatvies today, thankfully!

Dr. McCrindle reported that the results of his ecg are unchanged from his last ecg in August. No change is good, it means his heart is still functioning how they expect it to after a Glen surgery. His Fontan surgery is likely to be between 18 months and 30 months of age....but this estimate changes every time we see the cardiologist so we aren't counting on anything concrete.

Tyson also saw the audiologist today to follow-up on his hearing. We are happy to report that there is nothing wrong with his hearing!! We weren't surprised at this result because we haven't really been worried about his ability to hear, and he can already speak some words.

He now weighs over 23 pounds (bigger than my other kids at this age!) and he is eating and sleeping well. He is going to be one year old next Saturday and is still not crawling, but he is soooo close! He is able to pull to a stand with great effort and is starting to cruise around furniture. Once he starts crawling we're sure he will be motoring around like everyone else his age.

Some of you have asked if his heart will be "fixed" after his third surgery. Tyson's heart will never function normally. The surgeons have just "replumbed" it the best that they can. It is completely under-developed on the right side and the surgeries have made it so that the left side now does all the work, without any help from the right side. His heart will never function like a normal heart and will always need close monitoring to make sure it is still functioning well.

For Tyson's upcoming birthday, we will be hosting a come-and-go birthday party in the church basement on Saturday, November 21, 2009 from 10am-12pm.
Please join us there for some coffee, cake and refreshments.
Brian and Mel:)