Sunday, February 22, 2009

Home!!

Trey, Ali, and Cannon are home! Actually, they have been there for a couple of weeks, but have been having problems with the computer/internet. Everyone is doing great! Cannon had a couple of follow-up appointments this past Friday and all was well. Ali will post as soon as she can...get ready for LOTS of pictures of sweet baby Cannon!

Vesti

Tuesday, February 3, 2009

Almost there!!

Surgery went great yesterday...we now have a new shunt and they did his circumcision while he was under anesthesia. The night recovering was a little rough. Cannon had another breathing spell, actually two, where he quit breathing momentarily. I don't know why he does this, neither does anyone else. My suspicion is that his throat was irritated from being intubated. He did this before when he came back from surgery for his central line. Last night he did not want me to put him down, wouldn't lay in his bed. So we slept in the chair all night on my chest. It was a long night for Mommy,but we made it through. Today has been about resting and recovering. He has slept a lot, but has began eating better and better each feeding time. We are counting down the hours. He was supposed to get 48 hours of antibiotics after surgery before we can go home. Our afternoon antibiotic tomorrow will be 48 hours. So...we are very close to home!!!! We didn't see Dr. Roberts today so hopefully we will see him early in the morning and he will give us the all clear.
Thanks again for all your continued thoughts and prayers. They have carried us through this stressful and tiresome time. We love you all, and look forward to getting to see everyone once we get out of the hospital and settle into everyday life.
Love,
Trey, Ali, & Cannon

Sunday, February 1, 2009

Preparing for surgery # 5

We are scheduled for surgery at 7:30 in the morning. I have a feeling it will be a long night. Cannon will not have to stop eating until 3 am so that will help, but they will have to do neuro checks about every hour to make sure there are no complications from clamping off his external shunt. (meaning...his shunt is draining the spinal fluid on the outside of his body, into a bag. At midnight they will clamp that off. I'm not 100% sure why, but I'm thinking you would want some fluid in the ventricles of the brain when you go in to put the new shunt. This could possibly cause problems if too much fluid accumulates.) We are praying for no problems. So we will get a new shunt in the morning and come back without a bag, one less tube!! One step closer to home. The only thing left will be his central line, and he only gets hooked up to that every eight hours for about an hour. That will make us feel much more normal. Then we only have to have 48 hours more of antibiotics before we go home. YEA!!! I will do my best to update tomorrow with news on how surgery goes.

Now for some pictures...

These are more of our one month pictures.









After about the second one he just wasn't having it anymore...




We had to have a snack between shots...




Then he pooped in his outfit so he got a wardrobe change.




Pictures from today. Just chillin'




Grandaddy bought me a Tow Mater and he was getting ready to pull me out by my central line. :)




I am ready for the super bowl with my football clothes.

Daddy, Mater, Mommy, and Cannon


I just think this is so sweet!

Saturday, January 31, 2009

What A Month

It's been a long first month, but someone's happy tonight! While daddy is still out sick, we had a little birthday fun tonight (and yes, there were cupcakes). I caught this one while Ali talked to the nurse during a break in our "photo shoot." There are plenty more where this comes from...Ali will post later!



Happy "one month" Birthday angel baby! We love you!

Vesti

Thursday, January 29, 2009

Todays Photo shoot!

Here's what me and Mommy did today while Daddy was a out sick!





All this posing makes me tired!




Mom, I said I was tired.


What can I do to make her stop?
Maybe if I don't look at her...
Nope...didn't work...
Even when I'm sleeping
So Dr. Roberts came in today and said we are having surgery on Monday to replace my shunt. Another day in the OR...hopefully the last for a very very long time, I am tired of that place. Then I'll get a couple more days of antibiotics before I get to go home. I'm almost there!!! YEA!!! I can't wait, I was just starting get used to being at home in my own bed. And I miss my big, four-legged brother Hank. I can't wait to see him.
I am looking forward to a weekend full of visitors, my Grandaddy & Granmomma and Pawpaw & Grammie are coming. What fun that will be!! Well, that's all for today. Mommy says to tell everyone thank you for all your prayers, and for loving me so much!!
Love you all too,
Cannon
One last sweet picture before we go to bed.

Wednesday, January 28, 2009

Just Hanging Out!

Here's us just hanging out! We are just waiting, day by day getting antibiotics. I'm not sure how many more days we get. But we will just hang out here until we know Cannon's infection is completely gone. So far all of his cultures have come back negative. So we are looking good!
Sunday
Cannon got to finally meet his friend Drew and his mommy, Kim.




I finally caught a smile, of course he was sleeping. But it's SOO cute!
Thanks again to everyone for all your thoughts and prayers! We love you all!
Trey, Ali, & Cannon

Friday, January 23, 2009

Praise God!!



Praise God!!

Everyday is better than the one before. Thank you so much for all your thoughts, prayers, and concerns. I appologize to anyone who has texted and I haven't returned them. My head isn't as clear as I'd like, and I'm napping as often as possible. Vesti and I have sent Trey to their house so that he can get a good nights sleep and Vesti is staying with Cannon and I tonight.

So I'll back up a little and give a few more details, I'm thankful for all of Vesti's updates. I am trying to keep everyone informed, especially for prayer requests.
So Sunday night Cannon as more fussy than usual and I couldn't find a reason. After noticing that his head looked different, I felt his soft spot and it was bulging. I asked my mom for reassurance and she agreed. Trey called the neurosurgeon, Dr. Honeycutt was on call. (He is the surgeon we originally met before Cannon was born, and he was out of town when it was time for surgery...so we got Dr. Roberts) Dr. Honeycutt told us to come to the ER at Cook, so we quickly loaded up and headed this way. Thank you Sarah for helping us get together quickly and on the road. We got here about midnight and into a room around 5am. After a maybe a couple hours of interupted sleep, we were up and preparing for surgery. Mandy, the neuro nurse practitioner came in and took a sample of spinal fluid from the valve of Cannon's shunt. They were thinking infection as opposed to blockage because of it being so soon. As Vesti said, early results showed increased cell counts, pointing towards infection. We later found out it is a staph infection. That afternoon (Monday) Cannon went in for surgery #3. And how cool is it that before surgery Dr. Honeycutt asked if he could pray with us, he put his hand on Cannon's head and prayed over him and for all of us. It was AWESOME!!! They made a small incision on his right chest, and pulled out all of the shunt tubing leading to his belly. It is now draining externally, into a bag. They surgery went well, it only took about 15 minutes. They plan was to let the fluid drain on the outside while we treat infection. While in surgery they collected more fluid and sent it and the tip of the tubing for culture (this is how they check for growth, or infection). Cannon did pretty well waking up from surgery and did well recovering.



This is after Mondays surgery. The white circle on his chest is where his shunt is now coming out and is draining to the bag to the right of him.

Tuesday morning Mandy came back in and said that they wanted to put in a central IV line to give the antibiotics. For Cannon's sake this is best, however where was this thought Monday when we were already under anesthesia and on a breathing tube!! So another hard day! Surgery #4 wasn't as easy. It went well, but Cannon had a hard time recoverying from it. He didn't want to wake up, and his little throat was tired and irritated from having a tube put down 2 days in a row. He seemed to be struggling some with his breathing. He had Aunt Vesti and I very worried. And the pedi "on-call" took his getting up here and when he made his appearance said, "I think he is just cold, sometimes babies do that when they are cold". Of course by the time he got here Cannon was doing better. Not before frightening us though. It was a restless night. He wasn't eating, wouldn't nurse, and I was heartbroken.
Wednesay morning came and Mandy came to see Cannon. (I think it was Tueday an infectious disease doctor consulted and he swabbed Cannon's back for culture, he is also the doctor who gives the final word on what we do with antibiotics.) So looking at his back, Mandy says "when was the last time he ate?". My heart sank into my stomach and I wanted to get sick. NOT ANOTHER DAY OF SURGERY AND ALL THE YUCKY STUFF THAT GOES WITH IT!! I was upset! She said that she could see Dr. Roberts and Honeycutt going one of 2 ways. 1) watch it a couple days and see how it does 2) go back to surgery clean out the incision site and close it back up.

Cannon's incision has slowly opened up more and more. Starting with the carseat ride up here, then in the OR Tuesday they had put gauze over it and when it came off it pulled off the scab. Now it's wide open. But when Dr. Honeycutt came in he said it looked good and later Dr. Roberts came in and said the same thing. Dr. Mazade, ID (infectious disease) said the culture came back with infection, but it was a bacteria that is normal for an area so close to stool. And they aren't worried about it. After discussing it they didn't think we needed another antibiotic. So we are good to just watch his back, they felt like the tissue is healing and that it looks good! And today was a day of REST. Cannon slept a lot, as did Mommy and Daddy.

Thursday was another good day. We rested and tried to "relearn" to eat. And I got to nurse him, and he did well. (Restore my broken heart. Only a mom can understand the rejection you feel when they are not interested, esp. when they have been doing so well with it.) We are doing well with our antibiotic therapy, and Cannon is becoming more and more like himself. What a blessing! It's great to see him this way again.
Today was another GREAT day. He's eating very well. Can you believe that while Mommy was napping Aunt Vesti got Cannon to eat 4 1/2 ounces of my milk. He ate the first 2 1/2 in 11 minutes, then she gave a while to "feel" full, then he ate the next 2 ounces. WOW, Mommy is impressed!!! What a BIG boy!!

We also found out today that there has been no more growth on any of the cultures other than the original one that came from the valve. So Cannon's spinal fluid has so far shown no infection. I'm still a little confused how that works, but I'll take it.


Tonight the nurse came in and said that we get to unhook from IV fluids. One less tube!! Yea!




Can you believe he already picks up his head! 3 weeks old!