Thursday, January 29, 2009
I guess she's ready if she's negotiating...
Wednesday, January 28, 2009
Little humor for the morning...
Ok, Jenna has been following me around for 2 days begging me to let her open a can of Cream of Chicken Soup. She has no idea what it is, she just keeps getting the can off the shelf and really hoping it is something yummy. Well, I had finally had enough. I opened the can, and gave her a big spoonful....problem solved! Tuesday, January 27, 2009
What to do...what..to..do...


This was a butterfly made out of butterflies--pretty cool! You can see Gavin's scar pretty good too.
Kesley was very into posing for any picture...and I do mean POSING. I'm pretty sure she got this pose from some old pictures of me back in Aunt Lindas photo shooting days? Remember those! From the look of admiration on Jennas face, I think we will see this pose again very soon!

So that's where my camera went!

Friday, January 23, 2009
STARRING KESLEY!
Kesley has felt a little left out with all this attention being showered on Gavin. We thought she could use a little night out with dad and her own blog post. We didn't realize she was taking this so seriously, and really got a laugh when she showed up all primped and ready to go! I guess the Christmas make up isn't gone yet... Brent took one look at her and said they would most likely be heading to Payson for the evening! Gavin is home!
Wow! What a week. We got home yesterday afternoon and as soon as we walked through the door I just started bawling and couldn't stop! It seems the stress of the whole week all came tumbling out at once. The upside is I think I got it all out and this morning I feel great! 
I was happy he had this huge appetite because I knew he wouldn't be eating for a couple of days...that kid was a bottomless pit!

Poor G. He was EXHAUSTED from all the walking. It wasn't a ton of walking, but he is so breathless after just a block. I ended up carrying him towards the end. I just kept hoping this surgery would help him and that his life would change for ever!
Back at the hotel. Brent and G snuggling and watching T.V.....a favorite pass time of theirs. We sure lived every moment to the fullest that night. Funny how something like this just puts things into perspective and you become your best self. I wish I could be that kind of parent all the time....I think we all know that is IMPOSSIBLE! :) 
Gavin had such traumatic experience when they were trying to give him the anesthesia before his MRI two weeks ago. He wouldn't put the mask on and they ended up having to hold him down and hold the mask over his nose. It only took a couple of seconds, but they were a very scary couple of seconds that he did not forget. I was really worried about him having another bad experience this time around, but Liz had a great idea to wrap a present and tell him he could open it when he woke up. He would not let go of it the night before or the morning of. Great idea Liz!
The hospital also had a solution for this. They gave him this oral medication to relax him before they took him back to be put under. It worked REALLY fast and we had to lay him down in a wagon so he wouldn't fall over. I tried to read him a Winnie the Pooh book and knew he was going to do just fine when he started trying to "pluck" the cabbages out of Rabbits garden. Brent and I could not stop laughing!
The surgery went well and only took about 2 hours. Our Dr. came out to talk to us when it was done. He said that he has done a lot of these decompression surgeries and Gavin was "about as tight as they come" meaning things were really congested in there. He said G should see some real improvements in the next couple of weeks! Hooray! He said they would be moving him to recovery and we could go see him in about 1/2 hour when they had the breathing tube out and he was waking up and breathing on his own. Well....2 HOURS later they had still not called us back and we were beginning to loose it. Someone finally told us they were having trouble waking him up, but we could go back and see him one at a time. That was the hardest thing ever. He was moaning and his breathing sounded really raspy and slow. We tried everything to wake him up, but he was OUT! They said that because of his sleep apnea, he went into a deeper state of sleep and he was really sensitive to the anesthesia so that was also causing trouble....I don't know. Anyway, they couldn't keep his temperature or his oxygen levels up. After 5 hours in recovery the decision was finally made to send him to the NICU until he completely stabilized.
Here is G in the NICU. He finally woke up completely at about 8:00 that night--8 hours after coming out of surgery! Not a fun 8 hours for a parent!
He did really well after he finally woke up. By morning he was ready to be moved to a regular room and ready to open his present! He became known as "the kid with the car collection." Every nurse that came in had already heard about him and knew they would get the run down on all his cars! This hospital stay was more like Christmas than brain surgery! Here he is showing uncle "Joshy Boy" his cool new cars and then a picture with all his loot from all his visitors. Thank you EVERYONE for making things so fun for him!
So, this venture is officially over! He is doing great and even trying to hop on one leg---which we stopped quickly and he really paid a price for....probably won't be trying that again soon! He can't go to school for another week and is not too happy about that, but I think he is going to feel better and better everyday. Thank you all for all the prayers and well wishes.
Thursday, January 15, 2009
Gavin is headed for surgery!
We said OK to the surgery and then about DIED when he said, "I have a half a day open on Monday, will that work?" MONDAY! This is good because there is not a lot of time to worry, scary because it is only 3 days away! He will be up at Primarys for 3-4 days after the surgery and the recovery should be fairly quick after that--maybe a week or two until he is feeling great. One sad thing he said was, "This kid has probably never felt great. I think you will notice in a couple of weeks that he will be waking up and just be a whole new kid because he feels so good." I hope so!
We are very hopeful and feel at peace with this decision. Please keep him in your prayers. We Love you G-Man!
Thursday, January 8, 2009
Looking back and feeling bad...
I tell ya, this kid has ALWAYS been so uncoordinated. He has never been able to hold your hand and just walk without falling over. That has driven me crazy! He has never been able to run more than a couple of steps without falling over. I remember trying to make him run across a field and just touch the fence on the other side. Kesley was to the fence and back (at 2 years old) before G was half way there. He can't kick a ball, throw a ball, swing a bat or anything else without falling over! He can't do the monkey bars or climb a tree because he is just not strong enough (you've seen the size of his arms--skin over bone!). I have always just thought, "We'll steer him towards the arts...." This kid has gotten ART SUPPLIES for every birthday and Christmas in the place of sports equipment.
This diagnosis not only explains why he is so uncoordinated, but it also explains his excessive drooling, cough because of the extra drool, sleep apnea (which could also have been causing some things in and of itself), headaches that have been getting so much worse, arm and leg aches, shortness of breath, inability to breathe if he starts crying or gets too upset, THE LIST GOES ON AND ON! It makes me so sad!
The good news is, the surgery should cure him of a lot of his symptoms! It's not an easy--in and out--surgery. He will most likely be up at Primarys for a week after, but in time he should be great.
Wednesday, January 7, 2009
Gavin Update

Chiari malformations (CMs) are structural defects in the cerebellum, the part of the brain that controls balance. Normally the cerebellum and parts of the brainstem sit in an indented space at the lower rear of the skull, above the foramen magnum (a funnel-like opening to the spinal canal). When part of the cerebellum is located below the foramen magnum, it is called a Chiari malformation.
Friday, January 2, 2009
Christmas Eve and Christmas morning!

Hooray for my kids who slept until 7:00a.m.! The kids love to come out to see their present from Santa waiting for them. Santa's helpers must spend HOURS wrapping their presents! All the presents from mom and dad pale in comparison--next year mom is going to wrap as she buys so that her wrapping job isn't so....thrown together at 2:00a.m.!
Gavin loved his robot that Santa brought! He was extra happy when he took all his money from all the Grandparents combined and bought this extra cool remote control truck!
Kesley loved her new Pet Shop, but the real "hit" was the makeup she bought with her money from the Grandparents. Mom had no problem letting her GO CRAZY for a couple of days! My philosophy: The more you use the sooner it's gone! I brought up a big mirror for them to admire themselves in. Santa brought Jenna an entire trunk of new dress ups and they had a ball for hours! Notice Kesleys supermodel pose! She felt so beautiful--I let her wear this face to the extended family Christmas party and all the relatives got a good chuckle!


We had a wonderful Christmas!
Christmas Parties!





Family Christmas parties! We had some really great family parties where the kids enjoyed lots of cousins, an overwhelming amount of presents from the grandparents and were able to participate in 2 different Nativities in one night! Gavin was very disappointed he couldn't be the baby Jesus! Jenna and Kesley relished their roles as angels.

We are starting to get a little creative in finding parts in my side of the families Nativity. Jacob debuted as the star this year and Kevin was called, "the glitter boy!"
Quick updates for the scrapbook...
We made a stop to see his classroom on the way out of the school. Gavin has always talked about a little girl named, Shari. It's very cute and so innocent. I had to laugh when I saw the sentence he wrote for their sentence wall! He's said, in a very matter of fact tone, "I ALWAYS choose Shari to help when I'm the paper passer."
One of the better "play dates" we had this fall. Nothing can beat a fire, poking sticks and marshmallows! 

The first SNOW!! It seemed to take forever coming, but once it came....WOW!



See what I mean when I say "artsy!"
