HAPPY HALLOWEEN!!!!

For us it has been a really good Halloween. Here is Luke Skywalker and Princess Leah. They both just love thier costumes this year. They have been to a few different parties so they have definitely gotten a lot of use out of them.

And to join the crew, the NICU has costumes to dress the babies in and fittingly they had a little Yoda costume. So here is our little Yoda doing very well today.

I really appreciate Brent doing the blog yesterday. I had to go back and spell check it and I'm not so fond of some of the pictures he used, but for his first time ever blogging he did good. Although I don't know how he made everything a link?????? I love you Brent, thanks.

Like I said earlier today has been a good day. When we got here this morning we had good news. They took one more xray and the air in his chest is slowly decreasing so Cody's body is taking care of it by himself. So unless there is another turn for the worse, the doctor is not going to worry about it anymore. Also the pressure of oxygen Cody is on is decreasing as well, so he is doing more of the breathing himself.

This morning the nurse also decided we could try breastfeeding. The biggest worry is him asperating the milk into his lungs. We got to nurse really well this afternoon and did again this evening. It is such great progress for him. Hopefully in a few days no more feeding tube.

We are so gratefull for everyones thoughts and prayers. We have received so much help this last week it is unbelievable. Thanks again. Until tomorrow. bye

The last 30 hours have been some of the hardest. It started when we got a phone call from Cody's doctor on the way back to the hospital. when he found out we were on our way he waited untill we got back to talk to us rather than over the phone. you can know that that is never a good sign.Cody had lost his IV. Normally this is not such a big deal except that he has been stuck


4-5 times in each hand and food and every spot had failed. There was nowhere else to go. With no where else to go it was time to consider a more agressive approach to be able to get some nutrition in him. Cody's doctor wanted to use a type of IV that would follow his vein all the way to the heart. This line would be one of the last chances they would have to be able to get Cody the nutrition and medications that he needs. A wonderful team worked on Cody for a few hours trying to get in the needed lines but it was useless because either the vein did not have a direct coarse to the heart or it would not be strong enough and the vein would fail. Finally one of the nurses got another IV in his scalp and they were able to resume the nutrition and medications after several hours without anything at all.

In the efforts to establish the iv there were a few X-rays taken his doctor found Pneumothorax (An air pocket outside the lungs. Some where along the way Cody had blown a lung and was leaking air into his chest, and his lungs were beginning to collapse. The big blue nose that he wore (the c-pap) was to help create pressure in the lungs to keep them from collapsing in when he exhaled but now it was posing a danger by adding to the pneumothorax. Now what do you do... If you leave him on the c-pap it could push more and more air into the space between the lung and the ribs and if you take him off then his lungs could stick together from the inside and not expand to allow air in. The decision was made to take him off and put him on low flow oxygen. (seen in the picture above) To our relief Cody's ability to breath did not get worse so we watched him through the night. If he got any worse he would have to take a ride on life-flight to another hospital where the really sick children go.



Needless to say it was another sleepless night in the NICU. Cody did really well. The Doctor had started to feed some of the breast milk that we had been stockpiling through the tube into his stomach. At about 3 am after his feeding he woke up for a few minutes. It was good to see his eyes and hear him breath so well. He was stable enough that we came home for a few hours rest.



We went back about 9am when they let us back into the NICU. They had taken another X-ray and the air pocket in his chest was smaller. The low flow Oxygen pressure had been reduced a lot and Cody was doing very well. After lunch Mommy got to hold him again. It was a welcome moment of hope. Cody and Mommy as you can see were verry happy to be together again.





It's a good sign to see your child awake and responsive after what he has been through. Seeing him so happy and comfortable after such a hard day and night was a big relief to us. this next picture was when he was on the C-PAP. It's quite a difference with the picutre above from today.



for family home evening we carved our pumpkins with the kids.... they had a grand oll' time.





I guess this one ate just a little too much halloween candy.....


This is a good image to remember from today



Happy Baby!! Thank you for all your prayers. We know that the Lords hand is in all of this and that he will work all things for the good of his children if they will be humble and turn to him. Remember it's not about how the trial ends, we know that the day will come that we will see an end to all of our trials, So it is not about the way the trial ends. the scriptures teach us that what matters is the enduring trials well. So remember no matter how this trial ends, (and we know that it will), I pray that we may be found worthy having endured in faith trusting in God, Who's watchful care we are in.

Well this has been a really crazy week. Thursday we noticed Dallan's loose tooth really needed to come out. The new one was already behind it. So we gave him an apple and had him start biting. It took most of the night to convince him that if he gave dad one shot he could get it out really quick. He finally agreed and here is his tooth and the hole it left behind. He is way excited to show everyone at school and now he knows the Tooth Fairy is real!!!!



Friday October 24, 2008 We welcomed Cody Allen Palmer to our family. The doctor started me because last week the Ultra Sounds estimated Cody to weigh 8 lbs 6 ozs and we were afraid there would be problems if we waited too much longer.

We checked into the hospital at 7:30 am and he came shooting out at 3:40pm. The labor was pretty uneventful. We just waited around and once he decided to come he pretty much just fell out. So it was easy that way.

Cody was 7LBS 12 OZS and 20 inches long.

So he surprised us all by not being as big as we expected.

When we were being moved to our room the nurse noticed that Cody was grunting a lot and said we needed to check that out. Well, Brent went with Cody and they were gone for a long time. Cody's doctor came in and said there was a problem with his lungs so he was sent to the NICU. The ICU for babies.

Unfortunately that is were he still is. He has pneumonia for sure but there is some other problems they are trying to figure out. As of this morning they will probably be doing a spinal tap to check for viruses.

It has been hard not having him with us and Dallan and Allie are wanting to see him so badly but have to wait. They are not allowed in the NICU. So we will try and keep everyone up to date. It has been hard to call and talk to people. (especailly for me. I'm a hormonal mess) But please keep us in your prayers. Here are some pictures for everyone to meet Cody.

This is one of my favorite pictures. Right after he was born. He had his eyes wide open and they are big and bright like Dallan's. Brent was trying to get a picture or them but the flash made him close his eyes everytime.

Cody and Mom cuddling to get warm.

Here are some pictures from the NICU. His feet are very long. He wouldn't keep his foot tucked in and had it propped out. I am guessing this is the foot I felt trying to escape the last few months. He is definately a kicker. The second picture is him hooked up on the CPAP. It helps keeps his lungs inflated. I think it looks miserable. Poor boy. He is a fighter. He gets so mad at the nurses when they have to change his diaper or run tests. He has already pulled out one IV. Hopefully he will leave his new one in. It doesn't help to have to be poked so many times.

We will try and keep this updated for everyone. Love ya!!