Pre-Fontan Cath

We arrived in Houston late Tuesday night. Stockton was finally able to come down here and get this done. We arrived at TCH at 7am. Stockton was not able to eat after midnight. We were fortunate that we had an early cath time. We met with our anesthesiologist, David Vener, he prepped us for what he would expect and told us that he thought everything would run really smoothly. After that we met with our cardiology doctor, Aimee Liou. She would be the one performing the cath. She told us that she also expected things to run smoothly and explained to us that she would get a good look at Stockton's heart and she could see if there were any collateral veins. (If your heart isn't getting sufficient circulation or adequate oxygen it can begin to create little veins that help circulate the blood flood to certain areas. However, in a lot of cases these vessels can be a problem.) If Stockton has any of these then she will evaluate closing them off or not. A few moments later they gave Stockton some medicine to help relax him. He was acting really silly. We sent Stockton back about 9am. Seth and I were exhausted so we went down to floor 17 and laid on the chairs. We both fell asleep and before we knew it our pager was going off. The procedure was about 3 hours. We spoke with Dr. Liou and everything looks good. She told us that his body didn't create any collaterals. She did say that his pulmonary artery looked a little stenotic but that our surgeon, Dr. McKenzie would be the one to evaluate that. We had to stay by Stockton's bed for 6 hours. He was really sleepy but he was doing really well. When Stockton goes through these things he acts so big. He tried to drink but began throwing up. He threw up about 3 times before we ordered some Zofran. He improved greatly. He was so hungry. We left TCH about 5pm and we had so much relief.

The next day we met with Dr. McKenzie. He was very polite like he always is and was very engaged in our conversation. He said that he doesn't think he is going to touch Stockton's pulmonary artery. He also said that Stockton is getting really big and is a perfect candidate for the Fontan. We love Dr. McKenzie. He has been there since the beginning and we are clued to him. Dr. McKenzie has battle leukemia 2 or 3 times. We are grateful that he keeps coming back to work and we are so grateful for his knowledge. We owe Stockton to him. We left the appointment after having an hour long conversation. We are scheduled on August 7th, 2015 for the Fontan.

Grain of salt

My last post a few weeks ago was about our rescheduled cath. Well, we had to reschedule again! We canceled Stockton's cath because he had caught a cough which followed with some nasal drainage. We felt much better about canceling this time. (Gut instinct, I guess) So now here we are awaiting our new cath date, June 24th. As I write this I am concerned that he may have a UTI and just barely he complained about his ear hurting. Go figure. I am just going to take him to see his doctor tomorrow to make sure that he has no bugs. This poor kid is "healthy" most of the time. I have come to terms with being disappointed but yet I need to take it with a grain of salt.

Love them!

People often wonder what a day with Stockton is like. For some reason they think that because he has a heart condition that we don't do "normal" things. That is totally wrong. We get a lot of looks when we go to the public pool or to a water park because of his scars. I buy him a swim shirt but sometimes it makes him too cold. We are very fortunate with Stockton's case. He survived through the pregnancy, he survived through his first and second open heart surgery and he has surpassed the expectations that I had for him. Stockton lives a normal life and a lot of other children aren't as fortunate. I can't tell you how grateful I am that Stockton is somewhat healthy. He can communicate, like any other kid his age, he can feed himself, he plays with friends, he can can walk, he can swim, he can attend preschool, he can dress himself, he is a potty champ and many other things. We may have to be careful about how long he runs but we are so grateful for all of these other things that we weren't sure about 4 years ago. There are things that are different about him of course, he takes medication every day (only Aspirin, a miracle in itself), he takes naps mid day, he can't run as long, he gets hot & cold very easily, he has scars on his body and he goes to the doctor, a lot! We are grateful to have him in our lives.

When you meet Stockton, when you see the joy in his eyes, when you feel his strength and when you see his determination it truly is amazing. Stockton is going to do something great with his life, I can feel it. (He has already done so much already!) Tylee and Merrick are amazing, little human beings and they bring such joy into our lives. We have so much to be grateful for and I have a hard time dwelling on what we don't. It hurts me to see Stockton struggle and there is a lot of guilt. This will never go away, I've tried. We continue to learn from all of our children but we have so much to be grateful for. Our children are thriving, they fill our home with joy, they make me a better person, they are alive and I am blessed beyond words.

Merrick has the best smile.

Swimming in Arizona

Introduced the kids to DuckTales.

Summer Ice Cream

"Mom, I'm not tired. I don't want to take a nap." -Stockton