Monday, August 27, 2007

The first part of our journey



On your mark, get set, GO. . . read about my exciting, thrilling, action packed, and most of all mudane life. Well up until recently it was mudane. On July 6th I had my first child, Blake Matthew Hill. He was 17 in long and weighed in at a whopping 6 Ibs. I gave birth at 8:55 pm by the next morning he was at kosairs. The doctors found he had an interupted aortic arch(his arch wasn't connected to allow blood to pump to his lower half) and a moderate sized VSD(a hole in between his ventricles, the lower two chambers of the heart). They scheduled surgery for Tuesday, July 10th. They had to open my baby's chest up and he had to be put on the bypass machine. I had never been so scared. I remember thinking I just half to stay calm and think positive. I believe my husband and I did the best we could. Blake made it through the surgery he had to have his chest stay open for five days because he was to swollen for them to close. Those five days where the worst, especailly the first three. His blood pressure wouldn't stay up and his heart rate was to high. The doctors said he was just going along a little slower than they had expected. Finally on the 14th he started to turn around they were able to close his chest on the 15th. He was unintibated on the 20th and he was allowed to return to the NICU Monday the 23rd! Well he was doing pretty well up until last Friday, August 17th. He just wouldn't eat. He had to have his feeding tube put back in and that's when I found out about that his kidney's weren't doing well. Then Sunday my husband learned that he would have to have another surgery to fix stenosis(narrowing) in his arch. He is having his cath done tomorrow, they had to wait for his kidney fuction to improve. Since finding all this out, Blake's had alright days and so-so days some days he's seems so exhausted he had to have a blood transfusion last Friday his hemoglobin wasn't high enough. Here's to hoping everything goes great tomorrow. He's also been diagnosised with Williams syndrome. But I'll have to leave that for another post. Here's to hoping everything goes great tomorrow and if anyone reads this before than maybe you can say a littel prayer for my sweet boy.

10 comments:

Lisa said...

Whitney What a great picture!!! I am so glad you got your blog up now it well be much easier to keep tabs on you and little Blake...You are in my thoughts and prayers all the time...

Laura said...

Hi Whitney,
Happy to see your blog. I will keep Blake and your family in my prayers.

Noel said...

Whitney,
It is nice to get to meet you. I am another mom whose kid has heart/kidney problems with WS. Abi is 4.6 yr old though. I can only imagine what you are going through. My heart is with you and we are praying hard here too!!

Noel

Nancy said...

Nice to meet you, Whitney. Our son was about that size (5 lbs 14 oz) when he was born and has WS. He will be 3 soon, and he has the greatest sense of humor and, although my heart aches for him sometimes, he makes me smile A LOT.

I hope the cath goes well. We'll keep your family in our thoughts and prayers.

Heather said...

Hi whitney, I've been hearing about you and have been thinking about Blake. My thoughts and prayers are with you and your family... Hang in there, Heather

Heather said...

Oh yeah, When is your birthday? I'm a Libra too :) Sep. 30th ~Heather

Teresa and Shawn said...

Hi Whitney - Welcome to our blogging community! We have been praying for you and little Blake. My daughter Clare (2.5 years old) has WS and she has the heart issues as well. She has her sixth cath in a couple weeks. We will be thinking of Blake and keeping him in our prayers during his cath.
Teresa

camille said...

Hi Whitney, my husband and I have Connor, 2, who has WS. He is starting to chatter a lot now (basically in the background we have a constant "dadadadadadada" or "unda unda unda").

We will be praying for you guys tomorrow. I hope everything goes as smoothly as possible.

Kerry said...

What a cutie your little Blake is! Welcome to the blogging world, Whitney! My son Brady has WS and will be 2 in October. The support you will find online is amazing - always turn to it if you need anything. Good luck on Friday, we'll be thinking of you both :)

Julie said...

Hi Whitney,

Nice to meet you. Blake is such a cutie. My son Noah is 19 months old and has WS. He had surgery last July to repair the narrowing in his Aorta. Your family is in my prayers.