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!

Information About Tyson's Next Surgery

Hi there! Today we received a phone call from a member of Tyson's surgical team informing us of his next surgery. Tyson's surgeon Dr. VanArsdale and his cardiologist Dr. McCrindle, as well as their team of experts, have decided that Tyson will need his next surgery within the next six weeks. The date that they have scheduled Tyson in is Thursday, April 9, 2009 (the day before Good Friday.)

For the Glenn surgery, the surgeon will connect the Superior Vena Cava (SVC) directly to the pulmonary artery. The "blue" blood then goes directly into the lungs instead of through the heart. The BT shunt that was placed between the pulmonary artery and the aorta in the Norwood operation (on Dec. 4/08) will also be removed. This also means that we no longer have to inject our son's legs with needles twice a day, since the danger of blood clots is minimized and he won't need the blood thinners. When we asked Dr. McCrindle if he would need the needles after the surgery he said, "Probably not." Here's hoping that things go as planned and we can do away with those needles and see Tyson's legs without bruises for once (well, at least until he becomes a toddler and gets his own self-inflicted bruises!)

Lately Brian and I have googled the names of Tyson's surgeries (Norwood, Glenn and Fontan)and his various heart defects and we have come across some blogs from others who have children with similar heart surgeries. We are amazed at God's goodness and grace to us and to Tyson since he doesn't seem to be hitting as many speed bumps as some of the others in his shoes. Others in his situation have spent prolonged periods of time in the hospital, or have had additional surgeries due to complications (like gall bladders removed or eye surgeries), or have had to stay on the feeding tube for over a year after surgery, have difficulty gaining weight....the list goes on.
So far Tyson is gaining well (he's over 13 lbs now), he sleeps well (from about 9pm-4:30am), and he behaves like any of our other babies. He doesn't seem to be behind developmentally (although this may change after the next surgery since he won't enjoy spending time on his tummy anymore for a while, which may impede his ability to crawl.) He is almost four months old and he smiles, coos, laughs, responds by kicking legs and flapping arms when we look at him or talk to him, he enjoys time in the excersaucer and jolly jumper....so far so good! (We tend to compare him to his cousin Mikayla from Jason and Melanie, who is four weeks younger than Tyson - see pic to the left.)
Needless to say, we are thankful that we didn't view these web pages before Tyson's first surgery because I'm sure we would have been very scared! We are grateful for Tyson's progress in every area of his life and often we look back at past blog entries and think to ourselves, "Wow, he really has come a long way!" All evidence of God's goodness and reason to give thanks!


That's all for now!
Brian and Mel:)

Pre-Glenn Heart Catheterization - Monday, March 2, 2009

Tyson had his heart catheterization today at Sick Kids. Things went so well that we did not have to spend the night afterall and we were able to go home at 2 pm already! Basically the heart catheterization involved sending a catheter through his groin to his heart, injecting a dye, and measuring his heart's pressures, blood flow, etc. It's a standard pre-Glenn operation procedure. (his next operation is called a Glenn operation.)

My Mom, Tyson and I left Orangeville this morning at 4:45 am, arrived at Sick Kids by 6:15 am....checked in by 6:30 pm. Tyson was first admitted to a room on 4D, the same room where he stayed in December. The nurse came in to do a set of vitals, then the fellow cardiologist checked him over. At 8 am they took him from my arms and began the procedure. He was starving by the time they took him, since he wasn't allowed to eat past 4 am. Luckily they gave him gas to make him sleepy before inserting the IV line for the anaesthetic, because I don't think he would have laid very still for them while they attempted to put in an IV line! (He was MAD by the time they took him from me. And I wasn't allowed to stay while they anaesthetized him, but in hindsight I don't think I would have been able to handle seeing that.)

The doctor came in to our room at 9:25 am saying that the procedure was done and that they were in the process of trying to wake him up. At 10 am we were allowed to see him, at which time he nursed well and then went back to sleep. He was pretty puffy from the procedure. His sats (O2 levels) were a little lower than normal but after giving him some oxygen for a few hours, he seemed to bounce back just fine. Tyson stayed in recovery for a few hours and then he was discharged at 2 pm. We haven't received any results yet but if there was something concerning, a cardiologist would have informed us and we wouldn't be home right now!

We see Dr. McCrindle again on March 18 so if we don't hear anything from him in the meantime, everything is probably fine. We shall wait and see what he has to say and maybe from there we can find out an approximate surgery date, or month even?

That's the update for now. We are very thankful that we didn't have to stay the night and that Tyson bounced back quickly! Again, we see the grace and mercy of God!

Brian and Mel:)