Liver Functions and Solid Foods!

Hey there again! Trent is off work today and Cannon is asleep in his arms, so this is my chance to write a quick blog!
Well, Cannon has been out of the hospital (his 2^nd stay) for almost 2 months now. He’s been home and doing great. He is continuing to look better as far as his liver function levels go. He doesn’t look near as jaundice as he did. He had a Dr. appt. with his G.I. Dr at ACH on Sept. 22. They all thought he looked GREAT! His lab work also showed that his liver is doing great! As I had suspected, but didn’t want to get too excited over in case it wasn’t doing as well as I had thought! His direct Bilirubin had come down to almost normal. It is .6 (normal being from 0-.4) This was a big change from his last appt. His total Bilirubin is 1.0 and is in the normal range! His liver is functioning well and repairing itself! God is answering prayers!
At his last G.I. Dr. appt. we learned that they wanted him to keep his g tube until the spring. We were hoping they would let him get it out, but they want him to have it during the winter just in case he gets sick and doesn’t want to eat so he can still get his nourishment. As bummed as we were that he couldn’t get it out, we definitely agree with the Dr's. And feel this is a wise thing to do. He is after all high risk for illness. Please pray that this will be an easy winter for him and that he won’t get sick!
He is continuing to gain weight wonderfully! His dietitian has finally decided to let us let Cannon sleep as long as he wants in the night. Well, as long as he does not want to sleep like 10 or 12 hours without eating. As of now he’s doing about a 7 hour stretch at night without eating. So we are getting a little bit more rest. However, I am still up and down with him all night long even though he’s not actually up to take a bottle. He has to burp often due to his reflux and T.E. Fistula, so I am now sleeping in his room with him. So when I hear him squirming around in his bed I have to get up to burp him to keep him from refluxing milk up through his nose. So I have a lot of long nights of getting up and down to burp him. The nice thing right now is he doesn’t really wake up so he goes right back to sleep when I lay him down! (Knock on wood that is how it will continue to go until his reflux gets better!)
We were promised by his dietitian and G.I. Dr. that when his direct Bilirubin was at 2.0 or below he’d get to go on a different formula. One that tastes BETTER! FINALLY! Poor child has been drinking some yucky stuff mixed with his milk since his last hospital stay to help him put on weight. So we were excited to try out his new formula yesterday! He LOVES it. We went from fighting on some of his bottles with him spitting part of it out to he isn’t hardly dribbling a bit of it out of the side of his mouth! Ha-ha! I hated having to give him that other stuff, but I had to get some weight on that kid! Anyways, he’s not looking back! Ha-ha! The unfortunate thing is we had just gotten 6 or 7 cans of his old formula! I don’t think he will finish those off at this point! If anybody knows anyone whose child is on Pregestimil please let me know.
As of yesterday Cannon started on solid foods! This is a major milestone for him because the Dr's. Keep telling us that as he is able to take more solid foods his reflux will get better! He let us know VERY quickly that he HATES plain rice cereal! So I mixed some pears with it and he LOVED it! He also loves plain pears! It’s really funny to see him try to take food off a spoon. He’s a little used to a spoon because that’s how I give him his prevacid, but the new texture is confusing him a little bit. But he’s acting very excited about these new foods he’s getting to try! I am so excited to see him enjoying them and am praying that as he gets more his reflux truly will get better!
He is quickly outgrowing his newborn clothes and some of his 0-3 month clothes he has been able to wear! I know, I know…We have a 6 month old that is still wearing newborn clothes?!?! But hey, he’s come a long way. First he started out not even getting to wear clothes. Then he made it to preemie and stayed in that size for a while! Now he’s stayed in newborn size for a while too! But now that he’s gaining weight better it seems I looked at a few of those 0-3 month outfits and thought “oh those would be huge on him!” Now I’ve looked up and had to dress him in all of them this week because they are getting tight on him and he hadn’t even worn them yet! Ha-ha!
Cannon is finally letting us put him down some! In my last blog I wrote that he wanted to be held all the time. While he still prefers to be held, he is letting us put him in his swing and bouncy seat a little more. He does not really want to take naps anywhere except on someone! Which is fine by me because most of those naps are taken on me, and we all know I need a nap too! Like I said before, I’m up and down all night. And yes, that is making me SUPER exhausted! So I do not mind the extra nap I get when Cannon needs to snuggle up on me in the recliner!


Just loved how his eyes looked here.



Supporting those Hogs!



Talking to my toy!




This look makes me think that I'm going to have my hands really full!




So my dad decided to buy a convertible while Cannon was still in the NICU...This was Cannon's first time to go riding with his Grandaddy!




Rockin' my sunglasses!




Love this picture!  He's so cute!




This picture just made me smile.  His faces crack me up!




Talking to my mom and dad while strolling around the block!

 Love,
Christian, Trent, and Cannon

HOME!!!!!!!!!!!!

Ok, it’s been a little while. Once again! OF COURSE! And I can’t say it will get any better because when I’m home alone all day with this little boy of ours it’s hard to get anything done, let alone sit down at the computer to write a blog!
So, as it already says WE ARE ALL HOME TOGETHER AS A FAMILY! FINALLY!!!!!!! When I wrote the last blog I mentioned that we were hoping Cannon would get out of the hospital within the next couple of weeks. Well, it happened. We finally got to bring our special guy home on June 24, 2011. What a special day. We’ve had some pretty crazy times! Cannon had a rough time of it for a couple of weeks when we got home. I’m not going to go into detail because it was so scary and upsetting and I just don’t feel like recounting it all! I want to forget it. Honestly, I was looking for the returns department at the hospital so they could fix him again and then send him home. But when the times were going smoothly it was great. It was so wonderful to finally have this child home.
So fast forward 3 weeks. We returned to ACH to do Cannon’s follow up appointments. I had been in close contact with one of the dr’s nurses and I had told her a few days before our appt. that I thought Cannon’s jaundice had worsened. Well, I was correct. We left the first appt. with the neonatologist who had said he didn’t like how jaundice Cannon looked and headed to the appt. with the surgeon to hopefully get his g tube out. Well, the dr. had called the surgeon and said he needed Cannon admitted to the hospital to start running tests because in the time it took them to run his lab and us get to the surgeons office they had found out through the lab work that his jaundice level had in fact worsened. And quite a bit! So back into the hospital we go (for what ended up being a 12 day stay!). Of course, he could not return to the NICU where he had 5 primary nurses. Ugh. I was NOT happy about this even though I knew it before we got there. I did not like the new floor we were on, although I eventually adjusted. They ran several tests and scans and finally decided to do a liver biopsy. It was incredibly scary going through all of this and seeing the “laundry list” of issues that can go on with the liver and wondering which one of all these things could be going on with Cannon. We finally have all the results back from the liver biopsy and everything is normal. They determined what he had is TPN cholestasis. This is due to him being on TPN and lipids for such a long time and at such high doses before he was able to have his repair. We knew from the beginning he would have some liver damage from this, but unfortunately it was necessary for him to grow to have his surgery. So they have him on meds for that and it is very slowly getting better. We are praying that over the next few months everything will normalize on his lab work.
Also while he was in the hospital he was dealing with not gaining weight. While we were home the first time home health was coming over to weigh him each week. On their scale he was showing a good weight gain. So you can imagine our shock when we got to the dr. at ACH to find out that he had only put on ONE OUNCE in the little over 3 weeks that we had be home!!! Trent and I were so upset. I asked the dr’s. if this was something I had done to him because I had been feeding him the amount they told me to feed him and increased the amount each week like they had told me. I felt like a horrible mother! They reassured me that it wasn’t my fault, but of course as any mom would I still felt like it was something I had done. So now the dr’s. and dietitian have him on some formula mixed with milk that is for babies with fat malabsorption problems. He is gaining weight wonderfully now! This weight gain issue could be secondary to the liver issues he’s having. So we are praying that as his liver gets better his weight gain will get better too. Right now they still have us waking him in the middle of the night to feed him. He is on a 2.5-3 hour feeding schedule during the day and eats every 4 hours at night. This kid wants to sleep through the night, but he has to be able to take more volume during the day and keep up his weight before the dr’s will let him start sleeping through the night without feeding. We are all exhausted from this night schedule! Haha! But it will get better with time and we want to do what is best for Cannon! So please continue to pray for God’s healing hand to be on Cannon and make him better.
On a lighter note, it has been so fun to watch Cannon as he has become much more alert. He has the biggest and brightest smile. He “talks” to us all the time! His little faces are so funny to watch. He is SO SPOILED ROTTEN! He wants to be held ALL the time! I rarely get much done. (Like this blog that I started WEEKS ago!) But that’s all ok because we love being entertained by this kiddo! He’s the most adorable thing Trent and I have ever seen! Now with all that said, I must admit I’m going a little stir crazy in this house! Since Cannon isn’t supposed to really be exposed to people and all we stay in as much as possible. I think it’s kind of wearing on all of us. And we are supposed to not have him around people as much as possible and this will last all the way through the “sick season” which will be around March! UGH! We just can’t risk him getting sick, but it is going to be a LONG winter staying at the house! So also pray I don’t go completely off my rocker! Haha!
So like I said it’s taken me weeks to write this blog. I’m not deleting everything I’ve already written, but Cannon did have his checkup with his G.I. dr. and with the neonatologist that saw him in the NICU. Both check ups went well. The appt. with the G.I. dr. revealed that his jaundice level is going down! This was fantastic news. The liver is trying to repair itself and is doing well at that. At his next appt. in a month we will discuss introducing solid foods to his diet. Also, as his jaundice level continues to go down he may get to come off his formula he’s on now with all the extra stuff to help him absorb fat and onto a regular formula along with milk. At the neonatology dr. appt. he said that Cannon is doing great for his “adjusted” age and physically and mentally developing wonderfully! He is strong physically and strong willed. He had all the right responses to the dr. and he said that his voice is strong and doesn’t sound raspy or anything from his repair. This is all wonderful news!
Thank you all so much for all the prayers for Cannon. Maybe it won’t take me so long to do a blog next time. No pictures this time. I have a ton, but haven’t uploaded them and before it takes me another 3 weeks to post this blog I’m just going to post it and do pictures later! Haha!
Love,
Christian, Trent, and Cannon

The ups and downs of learning the bottle and hopes of going home!



"See me in my scooter outfit?  And yes I can hold my paci!"

Yes, I like this picture of Cannon and Trent, but I also want to point out the picture hanging on his bed.  That is from big cousin Sydney and it says "Kennon is the best baby boy I ever saw in my hole intir life!"  So she spelled his name wrong (her mom will correct her one day, but we both decided we didn't have to heart to tell her now and she was pretty close since she guessed on her own how to spell it!)  And yes, I will show her little brother Carson this picture one day!  haha!  Too sweet!  Thank you Sydney for Cannon's picture...He has enjoyed it being in his crib!

He can hold the paci in his mouth, and looks like can knock it out of there on his own too!

Sound asleep on his daddy's chest!

Me and Cannon in the nicu!  I am so tired of having to scrub in and put on a gown to see my child!  Another thing to look forward to when we get to go home!

Poor guys!  Trent was going on about 28-29 hours of no sleep at the point I think!

This is the first outfit we bought for Cannon when we found out he was a boy!  I just thought I wanted a girl....Was I wrong or what!  I can't imagine my life without this little guy!  He's amazing!

Well, that's all I have for now!

Love,

Christian

Figuring out the bottle has been a little bit of a challenge for Cannon. We knew it would be, but were still hopeful that he'd just take right to it. Now it seems by my last post that I've told a little bit of a story because I said he was doing great with the bottle. That's true and untrue so let me explain. It is true that he was doing great with his bottle at the time I wrote that blog. He was getting very small amounts and he had just started on the bottle and had only had surgery 7 days before his first bottle. So yes, considering all of that we thought he was doing great! However, a few days into it he just was not really wanting to take the bottle, he was gagging on the milk, and would freak out everytime milk went into his mouth. His latch onto the bottle was great and he could suck on the bottle (because remember...he was great with his paci!) but when the milk would come out he would get this shocked look and start gagging and spit it all out. Poor little thing! So we finally had occupational therapy come in to work with him and see if they could figure out what was going on. Their idea was to lay him on his side! Call me dumb, but I never thought that laying a baby on his side to let him eat would make the milk flow slow down to where it wouldn't choke him! No wonder he was gagging....It was too fast! So we did that for a little while and he ate better, but still not the best. The drs. had us try a thickener to see if he needed a little more substance to make it go down easier and stay down since he has reflux, but he HATED that. He immediately spit up the little bit he took! After that incident on the next bottle it was like the light bulb came on! He was able to sit back up to eat and he suddenly had the suck, swallow, breathe of bottle feeding down! This "new great trick" of his started on Thursday. He has been doing amazing since then! I didn't want to get too excited over his first few successful bottles because I kept thinking he'd revert back or that it was just a fluke. But here we are on Sunday night and he's doing wonderful. Thursday was the first time he took his bottle great and then he started showing all the signs of really wanting to eat. He'd wake up crying and looking for his bottle. He'd latch on perfectly and a few times he's sucked down the whole bottle while I've been blabbing to his nurse before I even had the chance to stop him mid way through to burp him! It's been so exciting to see all these wonderful changes over the last few days! He went from not eating at all, to eating but fighting it and not really sure about it, to wanting to eat and getting upset that his bottle is done with and having to settle for his paci! Unfortunately for Trent the light bulb came on for Cannon right after Trent left to go back home for work this week! He has only been hearing how wonderful Cannon is doing! Cannon and I are ready for him to be back up this Thursday so Cannon can show his daddy how awesome he is at this feeding thing! He's still only taking 4-5 bottles a day. But before that we had to back him down from 3-4 bottles a day to only 2-3 a day. I was so disappointed because it was a step back, but it quickly turned around! He's also only taking about 27 mLs at a time and still getting feeds through his g tube! His regular dr. will be back from vacation tomorrow so I am very excited to see what he will have in mind to do next with Cannon as far as feeds go. They have been "scrunching" his g tube feeds this week to where he's getting it over a faster time period. It's hard to explain the scrunching thing, so I'm not even going to attempt b/c I don't want to run the risk of sounding like an idiot! haha! Anyways, maybe just maybe Dr. A. will decide to let Cannon try to take all bottles sometime this week and see if we can get him off these g tube feedings before we go home! Last week we just knew for sure he'd go home still taking feeds through his g tube and quite possibly having to do it with a pump! But he had this turn around so we have hopes of going home on all bottles! Come on Cannon show us how strong and amazing you are once again!!!!
NOW we are finally able to start talking about going home! Of course we haven't discussed it with Dr. A. yet because when he left for vacation Cannon wasn't doing so great on his bottles as he is now! But when he returns tomorrow he will see a totally different little boy! Now we are really believing we will get to take him home in the next couple of weeks! I am interested to see if Dr. A. will talk about going home when he gets back! HURRY UP MONDAY!! haha! Trent and I are already having that bittersweet feeling of what going home means. We are more than excited to bring our sweet baby home and start showing him off (a little at a time!)....but we are going to miss the little ACH family we have acquired! We love all of his primary nurses like family (and we look at them like family now b/c we spend so much time with them that they probably get sick of us!), and his drs.! It will be hard to say bye to the nurses especially! Photos of them to come......
Maybe just maybe my next post will be written from our home! We will see!

Cannon’s surgery, swallow study, and more!

Well, I’ve been giving tidbits of information on Cannon on Facebook about his surgery and swallow study and all, but I thought I’d give a little bit more detail here. So here we go!
Cannon’s Surgery:
Friday May 20, 2011 Cannon had surgery to repair his esophagus. The first part of his surgery was to disconnect the lower half of his esophagus from his trachea. We knew going into surgery that this was the very least they would be doing on this day. That part was a success! The next part was to put the upper and lower part of the esophagus together. All the weeks from birth leading up to surgery the doctors were not able to tell us whether or not this part of surgery would be able to be done. Cannon was born with quite a gap and they were not sure if they would have enough to bridge that gap. After a very long two and a half to three hour wait in the waiting room one of the surgeons finally came out to talk to us. He said that they had PLENTY of esophagus to work with and they were VERY pleased with how well the surgery went and how Cannon handled it. This is EXACTLY what we had been praying for all these weeks. We kept waiting on the doctor to say “but…..” And to our surprise we did not end up having to hear that! They said it could not have gone better!
He spent Friday and Saturday on the vent and by Sunday he had only a nasal cannula on low settings. On Monday he started getting 1 mL an hour of milk dripped through his gastric tube. On Wednesday his milk was upped and he started getting 2 mLs an hour through his gastric tube. Thursday he turned 8 weeks old, went off the nasal cannula, and started getting 3 mLs an hour of milk! By Friday he was getting 4 mLs an hour!
Cannon’s Swallow Study:
Exactly one week later on Friday May 27, 2011 Cannon had his swallow study. He needed this to make sure that before they started him on a bottle that he had no leaks at the surgery site. Trent and I got to watch on the screen as he swallowed the yucky barium! He took that stuff like a champ and went to town on that nasty stuff! It was really neat to watch it on the screen. He had NO leaks! Of course we already had a feeling of this since when they did his surgery it ended up not being as tight of a stretch to make the connection as originally thought. About 2 hours later he was able to get his chest tube out and start taking a bottle by mouth! The moment of truth…..
Cannon’s First Bottle:
He did great! Ok, so his first bottle was only a tiny 5 mL bottle, but hey…he’s got to start somewhere right?! It was a tiny little drop of milk, but he seemed to enjoy it! Hopefully he will get it all figured out soon. He’s not used to swallowing things all the way down just yet since he didn’t have to do that for the first 7 weeks of life, but he will get the hang of it. He’s doing very well. Friday was his first bottle (the tiny little 5 mL bottle) and by Saturday they increased the bottles to 7 mLs. And today he was having 10 mL bottles! He’s on cycles of feedings so he is still getting fed through his gastric tube along with the bottles. So today he went from having 3 bottles a day plus the g tube feeds to 4 bottles a day and g tube feeds. So far he is doing great with this. We just pray that as the volume of these feeds goes up he will continue to do great. And we also pray that he does not have horrible reflux. The doctors are optimistic and have been telling us the last few days that if everything goes well as they increase his calorie intake that he MIGHT get to go home in the next couple of weeks. Keep in mind that is BEST case scenario! It at least gives us something to hope for, but I also don’t want to get my hopes up either so I keep telling myself it could be way longer! Either way Trent and I want what is best for Cannon! So we are not pushing the doctors to send him home.
Trent and I greatly appreciate every single prayer that each person has sent up. We could not have gotten through all of this without God and prayers. He has definitely stood by our side and taken care and watched over Cannon through all of this. We hope to get home soon so we can slowly start introducing our son to the rest of our family and to our friends.

FINALLY 3 days before his surgery one of the drs. let us put a onesie on him.  So this is his first outfit!

Not sure if you can see the drip drop of milk in this bottle, but it is his first bottle of 5 mLs of milk!

My 2 favorite guys!

He's got a decent little cry and it will get stronger as time goes on!

The first time Trent got to feed Cannon!



Much love~
Christian

A day of good news....

Let me begin by saying that Cannon has been doing so well.  He's been steadily gaining weight and getting closer to having his surgery.  Today, he finally reached a milestone that I have been waiting for....waiting 17 days for!  lol.  I am proud to say that he weighs 4 pounds!  April 18, 2011 he weighed in at 3 pounds and 17 days later he weighed in at 4 pounds!  Yes, I know I just repeated it, but that's because I am so very proud of this!  Go Cannon!  Also, I am extremely happy to say that all the chromosomes tests the drs. sent off on Cannon have come back completely normal! 
We have been patiently waiting for Cannon to grow so he can have surgery.  In my last post I told what kind of problem Cannon has and that he'd be having surgery to correct the problem.  Here is a little more in depth description of the problem.  He has what the drs. refer to as a "pouch" that started out at a depth of 6.5 cm down the back of his throat and it is now at around 9 cm.  The bottom part of the esophagus comes up from the stomach and connects to his trachea instead of to the upper part of the esophagus or what is now referred to as that pouch.  So the surgery will remove the lower part of the esophagus from the trachea and hopefully connect it to the upper part of the esophagus.  I say hopefully because the drs. say best case scenario is that they can make the connection.  Worst case scenario is they cannot make the connection. Please pray that they can make this connection!  I don't even want to get into what will go on in Cannon's future if they are not able to do it now (he would be fine and eventually have the connection made, but it'd be in probably a year and with some issues to deal with between now and then).  We will cross that bridge IF we get to it and at that point in time is when I will explain it in further detail.  I am hoping and praying I don't even have to go there though!  Our whole family's prayer is that they can make all the right connections during this surgery!  However, even if they can do it all Cannon has a long road ahead of him.  Babies with what Cannon has have a lot of reflux issues and introducing feeding doesn't always go very well, and add the fact that he is premature...He's just got a long hard road to go down.  But he's a fighter and I have faith he's going to do just fine.
Speaking of surgery......Cannon's surgeons came by today to make rounds and they are putting him tentatively on the schedule for May 20 to have surgery.  This date could change as they said "tentatively" but it gives us a better idea of a time frame we are looking at.  Please pray that Cannon will be big enough and strong enough, and that he will handle the surgery well.  Also, pray that the drs. can bridge his little gap and make the ends of the esophagus meet.  Please pray that God will guide every dr. and nurse during and after his surgery and that Cannon will bounce back quickly and show us that awesome personality he's developing!!
Now for a few fun things....Cannon is looking like his daddy more and more everyday in my opinion (and our family, and our friends, and every nurse and dr. that has seen him!!! haha)  However, I think he's starting to act a tiny bit like me...He's wanting more attention and love everyday!  Today I stood by his "box" (as I like to call it...it's really an isolette or incubator..haha) for almost 2 hours and he'd have me hold his paci for 5 or 10 minutes while he looked around and then he'd fall asleep and spit out the paci and a few minutes later just as I thought it was safe for me to sit down he'd start crying again...Then we'd repeat!!  I loved it though.  Actually made me feel a little bit needed!  It's amazing how much of a sucker I've become for that little boy!  Anyways, he's filling out and growing and that's exactly what he needs to be doing!  Trent and I could not be more proud of him and we cannot wait to get him home and show him off!  I do believe he's going to be SPOILED ROTTEN by all that know him!

Right after he was born

The first time I held him

One of mine and Trent's favorite pictures of Cannon



The first time Trent held him

Another one of our favorite pictures of him

I got my first mohawk when I was just shy of being a month old!

Cannon's "fresh hatched baby chick" look...This is what happens to his hair after it gets washed and nobody smooths it back down!!

This is what he looks like without all the tape and mouth tube in the way!  I can't wait to see him like this all the time!

Ok, well this is all that I have time for tonight!  I could keep adding pictures but I have to call it quits!  Thank you everyone that has been praying for our sweet little boy and please keep the prayers coming his way!

Love,

Christian (and Trent and Cannon too I suppose.)

Along with being a premie.....

I will apologize that it's been a bit since I updated the blog.  But what am I saying...I've only done one blog!  It's been a wild and crazy ride and I've actually been really thinking about how to do this post.  Hopefully I will explain things to where everyone will understand and maybe I will get it all in the correct order.

Our precious son, Cannon, arrived March 31, 2011 via emergency c-section.  Early the day before as I was having my weekly montioring session the drs. were concerned about some heart rate decels that were showing up.  They ordered another session on the monitors and he had one decel that called for me to be rushed down to the labor and delivery floor for 24 hours monitoring.  Less than 48 hours later due to many decels the drs. called it and said I was having a c-section immediately!  I had all of about 20 seconds to take this in as they were wheeling me down to the O.R.  Trent was almost home and was going to work that night.  My dad was still at the hospital and he made all the calls to get family there a.s.a.p.

So I wake up in the recovery room to a dr. telling me that not only was Cannon a premie (which we of course knew from the get go) he also had esophageal atresia and tracheo esophageal fistula.  I was scared to death.  Basically, this means Cannon's esophagus does not connect to his stomach where it should.  Also it means his esophagus is connected to his trachea.  So, how does he eat?  How does he breathe?  What happens next?

He had surgery the day after he was born to put a gastric tube in.  This tube is in his stomach and it sucks out any fluid that gets in his stomach.  He also has a tube in his mouth that sucks out any saliva so that he will not choke.  He cannot have any milk or formula or anything.  He has a picc line that allows them to pump him up with lipids so he can gain weight.  He was born around 1 kilo (or about 2 lbs. 8ish oz.).  He will have another surgery (hopefully in a few months) for them to detach the esophagus from the trachea and connect it to the stomach where it belongs.  They origionally told us they wanted him to grow to be between 1.5-2 kilos (or up to about 4ish lbs) before they do this surgery.  However, today a surgeon came in to speak to me and she said that if he is doing well when he hits 1.5 kilos they want to keep him growing to 2 kilos.  Then if he's doing well at 2 kilos they will try to get him to 3 kilos (about 6ish lbs) before they do the surgery.  She said the bigger he is for the surgery the easier it will be on him and on them.  

It has really been a roller coaster ride of emotions and exhaustion. This is the basic gist of what is going on with Cannon and as we learn more I will update.  Please be patient and send prayers and love for our son, the little fighter!

Also I will post pictures towards the end of the week when Trent makes it back to Little Rock with my laptop.

Love,

Christian and Trent

Starting this blog.....Please be patient!!

OK, here I go!  Be patient as I am still trying to figure out how in the world to set up this blog!  I get frustrated easily sometimes when it comes to technology and well since I'm supposed to be as relaxed as possible right now it may take me a while to get it looking decent!  Bear with me!
I've been meaning to start a blog to be able to remember my pregnancy, but I never got around to it until now.  Now I have plenty of time on my hands to write and think about my pregnancy and what's going to turn out to be a shorter pregnancy than expected.
I have had a wonderful and very smooth pregnancy since day one.  Trent and I found out back in December that we would be welcoming a little boy.  He will be named Cannon and we could not be happier!  We cannot wait to welcome him, which will now be sooner than expected.  Like I said everything had been smooth sailing from day one until last Wednesday in the early morning hours.  At 1:45 a.m. Wednesday March, 23, 2011 I woke up with a rude awakening.....my water had broken!  I was what I thought was 31 weeks pregnant and it caught Trent and I off guard completely!  We immediately went to the Labor and Delivery floor in our local hospital and they called my Dr. in to come make sure things were OK.  They weren't.  I was prepared to be transferred to UAMS and told by a nurse I would be having my baby in 48 hours.  That scared us to death, but we remained as calm as possible!  I was transferred to UAMS and Trent and my dad followed and my mom met us here as soon as I arrived and Trent's parents arrived as soon as they could.  Exhausted and a little scared we met with about 10 doctors in the first hour or two we were here.  They told us several things.  Bad news was yes my water had in fact broken.  Good news was I was not contracting or going into active labor!  They moved my due date back from May 26 to June 5 due to an early ultrasound dating.  So that put me at 29 weeks and a few days (still not clear on how many days due to my exhaustion and being confused and just plain chaos going on!!  lol.. So you do the math!)  Anyways, they told us that I would be here in the hospital until I had this baby.  They are hoping to keep him growing and developing until I am 34 weeks.  At that point they will induce labor because the risks of infections and a couple other things increase and it's better to go ahead and have him instead of trying to go to term.  With that said, they will keep him growing until 34 weeks unless I go into labor on my own, show signs of infection, or signs of fetal distress.  They plan to take him April 24, 2011.  They are taking wonderful care of me and monitoring baby Cannon closely.
I am officially starting the hospital bed rest countdown..........27 days until we meet Cannon...we hope he cooperates and wants to keep cooking that long!  He does have a strong mind of his own so just be praying that he will do what we all are hoping for and stay where he's supposed until he's 34 weeks!
Thank you for all the thoughts, prayers, calls, and texts!  And for your patience as I work on this website to make it look better!
Christian