Sunday, May 26, 2013

The good, the bad and the ugly....(Part 1)

Hi little man,

You probably noticed that mommy didn't write you a note last weekend.  I'm sorry for that buddy but things were a little crazy.  To be honest things were more than a little crazy they were pretty insane.  I'm going to try my best to recap the past two weeks without writing a novel but I make no promises.  A lot has happened since our last note some of it good, some bad and some down right ugly.

Let's start out with "the bad" which unfortunately progresses to "the ugly".  Your daddy's last note left off after your appointment on Monday the 13th.  Tuesday we didn't have to be at anywhere but you did have two in-home appointments that went off without a hitch.  Early Wednesday morning you, mommy and your nurse Zion headed to the hospital for an early appointment.  As soon we as we got checked in you started gagging and spitting up (which is very unusual for you).  For the next several hours your heart rate was elevated, you were breathing fast and you just weren't yourself.  To make matters worse this wasn't a typical appointment but a clinic in which we had to sit in a classroom with a bunch of other babies and their parents for a presentation then wait in the waiting room for our individual appointments with the nurse practitioner and finally meet with the equipment company.  The purpose of this appointment was to fit you for a helmet since your head is so flat in the back from having to lay still for so many months in the ICU.  Mommy and daddy aren't too excited about this one since you are such a little hot box all the time and you don't exactly like things on your head not to mention we are heading into the summer months.  We know that it's something that needs to happen sooner rather than later but we still aren't looking forward to it.    Let's hope you surprise us as you have with so many things and just see it as a really cool accessory.



Wednesday was exhausting but by bedtime you had settled down and were acting like yourself again. We all assumed it was just an off day and whatever was going on had worked itself out.  Mommy was certain that you would be just fine and we convinced daddy that he should still go on the trip he had planned to Texas.  You tried to sneak in daddy's suitcase so you could go visit your Gigi, Grand dad Rooster, Uncle Sebastian, Aunt Alexa and Pappaw.  I promised they will all come to visit you again soon and before you know it we will be making that trip to Texas with daddy.  Although we couldn't all go mommy was very happy that daddy had a chance to see his family and give them hugs from all of us.


Thursday morning you made it clear that whatever was bothering you wasn't gone yet.  After much debate mommy and Grandma went ahead and took you to your pulmonology appointment that afternoon hoping they may have some answers.  The nurse and doctor spent several hours with you but after careful examination and some cultures they didn't find anything to be the cause of your issues. You did have some drainage around your trach for which they gave mommy some drops to clear things up but in the end no bacteria grew on the cultures.  We kept the Tylenol pumping through you and once again you seemed to settle out as the evening progressed.  Mommy really felt like you were over the hump and Friday we would be back to business as usual.


Mommy was wrong.  Friday morning started pretty rocky and this is where we move into "the ugly."   Mommy had to call the pulmonologist to give her a report since you had gotten worse from your visit the day before.  She wasn't able to see you and said you probably needed to go to the ER based on how fast you were breathing, your increased heart rate, low grade temp, gagging and increased work of breathing.  The other option was to see your pediatrician immediately.  Once again Wendy came to the rescue.  She was able to fit you into her schedule and back downtown we headed for the forth day this week.  Between doctor Hall and Wendy they literally checked every inch of your little body.  They did urine cultures, checked the respiratory cultures from the day before, x-rayed your chest and belly yet didn't find anything significant.  Because they had ruled out all of the extremely serious concerns we were able to return back home and check in with them over the phone.

The next two days are a bit of a blur.  Daddy was out of town, we didn't have a nurse either night or one of the days, and you were sick.  Thank goodness for Grandma and Grandpa.  Without them staying up half the night, waking up at the crack of dawn, fetching this, suctioning that, rocking you just so and feeding mommy I'm not sure how we would have made it through.  Things all kind of came to a climax Sunday morning when for the first time mommy thought there was a chance we were going to have to call an ambulance.  Thankfully Dr. Hall and Wendy had sent us home with an inhaler in case of such situation.   We were able to get your breathing and heart rate under control and as Sunday progressed you improved by the hour.  You were still fussy and tired but by Sunday night  your breathing was close to normal again and your heart rate was down.  You even squeaked out a half smile late Sunday night when daddy got home from the airport.   It took another 2 days for you to regain your smiley playful personality but it was obvious you were on the mend.


So what was the cause of such a rough few days you ask?   Good question.  Mommy has a few theories.  One is that you got your first tooth!   That's right between Saturday and Sunday your first pearly white peaked through your pink little gums.  Mommy also realized that we had weaned another one of your medications the previous week so you were still getting the night dose but not the day time dose which may have explained why mornings were so rough.  Lastly you had a lot of extra secretions and there was this new gagging maneuver that you had learned.  The week before during your scope Dr. A had removed some scar tissue from above your trach.  Mommy believes that this now allows you to cough up a lot of the secretions that you previously couldn't move past your trach.  Because you aren't used to this you haven't quite figured out what to do with it and mommy believes it is making you gag.

Although I hate that you had to go through such a rough few days I am extremely proud that you were able to work through it and not end up in the hospital.  You made it through 4 doctors visits in 5 days while being sick as well as a weekend without nurses or your daddy.  Mommy is super proud of how tough you have become and how much you are able to tolerate.  You have always been a strong boy but your tolerance and ability to bounce back from things is growing each week.

We still have "the good" part of the story left but mommy can barely keep her eyes open so I will write you part two tomorrow.  Stay tuned.........

Mommy and daddy love you Connor!

-Mommy

Monday, May 13, 2013

Tic Tic Tic...

Hey Bubbs,

So here I sit, finally, writing you a note to tell you about yet another big week in your little life. As I sit here with my headphones in, attempting to concentrate with all my might, your wonderful mommy and grandparents are doing everything they can to keep you awake and entertained and awake for another hour so you will be ready for bed and actually go to sleep at a decent time. You have been playing around with your schedule a bit and we are trying to get that roller coaster under control but we just aren't there yet. So we do what we can, which normally means lots of noises and faces and flashing toys. I find myself thinking "what am I doing?" and "does this help or does he think we are insane?" I guess we won't know but for now it seems to do the trick.

Before I get into last week and all the excitement I better tell you real quick about your visit with your Pappaw. He came up here and spent several hours with you and your daddy and we all had a great time together. We played and cuddled and he and I even got to take you outside with no tubes attached! It was pretty awesome to see you playing with him. I know he has been dying to get to play with you and you seem so happy when you see him smiling at you and making funny faces. Your Pappaw sure does love you little man.

Let me try to recount the last week now. I'll start with Monday. You had another appointment, thankfully this one was up north at the Liberty campus so both mommy and daddy could go with you. I know I don't always get to go with you and mommy to see your doctors but we are doing our best to make your appointment times later in the day when we can. Some doctors are busier than others though, so its a toss up. The appointment Monday was with your ophthalmologist (he is one of the busy ones). He needed to check on your eyes and make sure they were still looking as good as they were when we left the hospital and as a bonus (sarcasm is thick here in case you can't tell) they decided to test the pressures in your eyes because of the supposed clot that you have in your head. Well the regular eye exam went off without a hitch, you passed with flying colors and the doctor said he wouldn't need to see you again for several months. Right before that the nurse kept poking your eyeballs with some blue tipped pen until you went into full out "lose my ****" mode. They didn't get to test both eyes but the doctor felt confident you were doing just fine and the "clot" wasn't causing any excess pressure. I guess it is always better to be safe than sorry but some days I think you would rather take the risk and I can't blame you.

After that mommy and I took you around in the car for a while and you seemed to enjoy that. You seem to enjoy being in your car seat, at least while its moving. That is a good thing too, because you got to spend a LOT of time in it on Tuesday. You see Tuesday you had an appointment with your ENT doctor, Dr. A, so that he could check up on your trach and your nose job. You were supposed to be in and out and home for the night but about twenty minutes after we brought you in we were told there would be a delay of at least ninety minutes. That turned into two hours. That turned into four hours. That turned into six hours. The nurse in the pre-surgery floor actually starting cleaning all the rooms and turning off the lights before we got the call to tell us you were next. At that point we also found out for the first time that you were going to need to stay the night after this procedure. Apparently there was a mix up in scheduling and they forgot to tell us that beforehand so your mommy and I were badly unprepared. We didn't have enough milk, we didn't have any clothes for us to sleep in, we had enough for a six hour stay at the hospital but not for the twenty-four we were now facing.

So off you went to the operating room and we sat down and tried to figure out what to do for the night. We didn't have much time to think though, Dr. A was finished with you in a short thirty minutes and called us back to discuss what he had seen. As it turns out you did great, as you always do, and he didn't have a lot to report so no news was good news. He did tell us he was very impressed with how you were doing and that he had to remove a little bit of excess skin from your trach (it was a little scar tissue building up) so you could breathe better on your windows off the vent. Your trachea looked great otherwise and your nose had stayed open even better than he had imagined it would. All in all he was thrilled with you.

The next bit of good news we got from Dr. A was that you were headed back to your friends in the CICU for your little overnight visit. That made your mommy and I feel SOOOOOO much better. I am sure that any unit would have taken good care of your but we know you hold a special place in the hearts of the people up there and they take care of you like family. As a matter of fact we hadn't been up on the sixth floor for twenty minutes when one of your favorite nurses burst in and gave mommy a hug. It was heart warming to see the love on the faces of the nurses and doctors and RT's who got to take care of you that night. Maybe it sounds a bit sappy but for almost six months of all of our lives those people were just as much family as our real family so to see them just warmed our hearts.

Since your visit was kind of a surprise no one knew what you were coming in for and of course everyone was worried to see your name on the nursing board. It was so much of a surprise in fact that the OR nurses called your buddy Dr. Cooper and said "we have Connor Logsdon down here, would he be able to stay there overnight?" and he responded with "Connor? We love Connor, bring him on up!". I think he was excited to see you. Then once the nurses realized you were just visiting on a routine trip to the hospital they were all back to "oohing" and "aahhhing" over you like they always did. You saw some of your favorite nurses in those twenty four hours and you seemed pretty happy about that.

So the next morning mommy got you all packed up and ready to go and you had to say your goodbyes. It was great to see your friends but as wonderful as those people are you belong back at home these days and it was time to get you back there. Over the next two days you got to see your speech and physical therapists. They couldn't get over how well you were doing and how much progress you were making with things like rolling around and holding your head up. The PT even told mommy that she was impressed with how hard a worker you are. Personally I think that has a lot to do with all the hard work mommy does with you during the days. It seems like every day she is telling me stories about some new wonderful thing you are doing. Pretty impressive.

Compared to the first half of the week the second half seemed like a breeze. You were pretty content and once we got you back to a normal sleep schedule after an apparent all night party in the CICU things were back to normal, whatever that means these days. We spent a nice relaxing weekend and celebrated your mommy's first Mother's Day. She didn't want anything except to sleep in a little and spend the day cuddling with you. Mommy watched movies and cuddled you on the couch while your daddy and grandpa tried to take care of everything. Grandma even got some time to herself and then we all had a great dinner together, including you right there with us.


Speaking of eating, you have been doing some good things with food lately. Now you didn't get to do the usual baby thing and eat from a bottle (meh, who needs a bottle anyway). Instead you jumped right to taking baby food from a spoon. You aren't exactly gorging yourself at this point but you are taking small spoonfuls and swallowing it. That may not sound like much but let me tell you it is a BIG deal. We were worried that would take you months or years to get to but you have yet again gone above and beyond and surprised us all. I hope you never stop doing that little man.

One last little note to sneak in before I wrap up this novel. Today you went with mommy to see your hematologist, the one who was convinced there was a clot in your head, and you walked away with good news. Not only do they believe that the "clot" is no longer an issue and you therefore don't have to get your Lovenox shots anymore but your blood counts were all stellar and you don't have to have your iron supplement anymore either. Combine that with the one less dose of Neurontin you are getting this week and you have knocked out a good chunk of your med sheet. Keep going buddy and before you know it we will be down to just a few meds here and there. I can't wait, and I know you can't either. Tic Tic Tic, three more things off the list and counting down.

So keep up the good work little man, keep being so strong and keep working hard. We are so proud of you.

Mommy and daddy love you Connor.

- Daddy



Monday, May 6, 2013

A day in the life of Connor

Hi Little Man,

(Now that's an outfit...OH.....IO!)
A lot of people have been asking mommy what a typical day is like for you at home so I thought I would start out by briefly running through one.  I also thought it might be nice to document what life is like right now and then compare it where we are in a few months.

-5:40am  Mommy gets up (Daddy is already long gone for work and the gym, that's beyond early).
-6:00am Your nurse Stacy leaves if it's Monday-Friday morning (if it's the weekend either mommy or daddy have probably camped out on the air mattress in your room).
-7:00am You get some medicine in your G tube and mommy mixes up some milkshakes for you (we fill these up every 4 hours around the clock).
-8:00am You get 4 medicines through your G tube and your eye ointment.  You typically wake up about now and need lots of suctioning for the next hour or two as you get things moving.  You like to play quietly by yourself when you first wake up which gives mommy a chance to drink her coffee and stock up on all the supplies we will need for the day.
-9:00am You get one G tube medicine, your injection (blood thinner), and then mommy cath's you.
-9:00-11:00am We play, do our stretches, work on your therapy exercises, clean your G tube site/dressing, take a sponge bath and get dressed for the day.  We also do one of your hour windows off you vent during this time and try to wear your hearing aide on days that mommy is able to keep it in your ear. 
-11:00am Grandma and Mommy do your trach care
-11:30am You take a nap (sometimes this is a real nap other times its a 20 minute power nap).  Grandma usually hangs out with you during this time and plays with you if you're awake so mommy can shower and eat something.
-12:00pm You get 3 more medicines in your G tube and eye ointment
-2:00pm We typically move from your room into the family room and before long daddy comes home.  You and daddy play together and do some work on sitting up, reaching and other important things.  Together we all play on the floor, sit on the couch, spend a little time in your swing or bouncy seat and do whatever we can to entertain you which more often than not results in us being entertained.  You usually do your second hour window off the vent sometime during the afternoon and on good days we try and give your hearing aide another go.
-4:00pm You get some medicine to help you go to the bathroom which results in you promptly blowing out your diaper plus you get some more eye ointment.  Most days you take a little power nap around this time.  By now Grandpa is home from work and dying to get some play time with you. 
- 6:00pm The Connor train moves it's way out to the kitchen where we set up camp for dinner.  You usually play quietly and watch us all eat dinner besides needing suctioning here and there.  After the grown ups finish eating mommy and daddy try and do your tastings as part of speech therapy.
-7:00pm  You get one G tube medicine and we head back to the family room after changing out your feeding bag for the day.
-8:00pm  You get 4 G tube medicines and your eye ointment.  During the next hour we take turns hanging out with you (trying to keep you awake and happy) while getting the night chores done such as changing out the suction equipment and cleaning it, changing out part of your ventilator, thawing out milk and making bottles for the night and cleaning up our mess from the day.
-9:00pm  Time for your injection again and cath'ing (usually daddy does this).  Then off to bed you go.  Sometimes you fall asleep instantly and other nights it takes you a while to drift off.  On those night we try and read a book and cuddle.  Although it may take a bit to get you to sleep you almost always sleep well through the night once you are asleep.
-10:00pm  Your nurse Stacy gets here so mommy and daddy fill her in on the day and then try to get some sleep ourselves.
-4:00am  You get 2 G tube medicines and more eye ointment.

Right now that's a typical day in the life of Connor assuming you don't have any doctor's appointments (you average 3 a week) or any therapy sessions (right now the therapists come to our house 2-3 times a week).  We are starting to learn how to juggle your schedule around appointments, naps, and the million other variables that change on a day to day basis.  Luckily Grandma and Grandpa have been an enormous help to mommy and daddy so with some team work we haven't missed a beat yet.  You also have a day nurse two days a week that is also a big help.  Her name is Zion and you seem to enjoy hanging out with her.  This week your full time day nurse starts so that will be a big help and adjustment for mommy and Grandma during the day.  It's kind of hard to keep up with all your daily care, the phone calls, appointment scheduling, insurance crap not to mention regular things like laundry when all mommy really wants to do is play with you.  We are already getting more efficient with everything so I know over time this will all be very routine for us.  Plus in time there will hopefully be less and less medicines, appointments, and procedures making the days easier and easier.


Speaking of appointments you got an A+ from both your pediatrician and cardiologist this week and you were a champ during both appointments (which is impressive considering one was at 6:45 am and you had to get stuck twice for blood work).  Your pediatrician, Dr. Fletcher was thrilled with how well you have adjusted to home life.  You have gained a little weight since you've been home, done great with your windows off the vent and all of your blood work is stable.  We sure feel lucky to have Dr. Fletcher and his whole team on your side.  They are amazing at keeping all your issues sorted out and coordinating the billion specialists involved in your care.   Your little heart got the stamp of approval from Dr. Hirsch at your cardiology appointment.  He repeated what an amazing little boy you are and he couldn't be happier with how your heart is working.  He said your repair is excellent (thanks to Dr. Morales) and although we have to keep an eye on one of your valves your heart is much lower on the list of priorities that need attention in the near future.  Awesome news !

(You played contently for over an hour on the doctor's table)
We did have one pretty rough day this week.  On Wednesday you weren't yourself at all.  You were spitting up, had a little fever, were very restless and your heart rate was much higher than usual.  Your nurse Zion was here during the day and she was pretty worried about you.  Mommy was hoping with all her might that you would settle out but as the day went on things seemed to get worse and worse.  Twice mommy actually packed the car thinking we would be heading down to the hospital but you pulled through and we were able to stay home.  Mommy is so thankful for one of the nurse practitioners that works with Dr. Fletcher.  Her name is Wendy and she called every two hours to check on you and give mommy orders for what to do to keep you home.  We still aren't sure if you had one of the many stomach bugs going around or if your yuckiness was a result of withdrawling from your clonidine patch.  So for now you have the patch back on but we'll get rid of it before long.  Although Wednesday was pretty rough by the crack of dawn Thursday you were back to your old self and flashing smiles at everyone in the cardiology office.






All in all mommy and daddy couldn't be happier to have another successful week under our belt.  Yet again you have impressed your family, friends, doctors, nurses and therapists.  Connor you are one remarkable little fellow.  I know there are so many more details of the week that I wasn't able to pack into this note but as you can see our days are a little busy and despite my best intentions I haven't had time to write you more often.  Time to get some rest and gear up for another busy week of appointments, therapy, visitors, and most importantly play time.

Mommy and daddy love you Connor.

-Mommy



Sunday, April 28, 2013

Big Things... (with pictures now)

(I hope you all complained to Apple about the new iPhone cord.... Here are plenty of pictures)

Hey Bubba,

So we have made it through another week and are settling in for the night to face the coming week. In the last seven days since our last note we have had a lot of stuff going on and have seen some pretty big things. It is kind of funny what is considered a big thing these days though. Big things don't necessarily have to be all that big relative to the rest of the world in order to have a BIG impact on you and your world.

Where shall we start? I guess we should probably start with easing the fears of your friends and fans who were left hanging off the cliff mommy signed off with last week. You pulled through your first cold (or at least we think it was your first cold) and are no worse off than when you got home. In fact, you may be better off because you know have a mommy and daddy who know that you can make it through a cold and a fever and barely blink an eye. We were worried for a few days and we discussed taking you to the hospital at least a dozen times in forty-eight hours, but the Tylenol worked and you showed us your strength yet again and we all made it through.

That was a week ago exactly. Since then you have been busy making progress in quite a few ways. Mommy mentioned last week that you have been doing a little moving and shaking and traveling around the house but this week you have been a traveling fool. You have been all over the house now, including the basement with daddy. You took another car ride and found yourself looking out the window at some of the neighborhoods of West Chester as your mommy and daddy tried to figure out where we will go when we are finally ready to move out of your Grandma and Grandpa's house. You really seemed to enjoy it for the first hour or so but after that I think you were ready for some home time and you let us know that.

You have also been working on your therapy a lot more, mostly thanks to your mommy and her skills. You have been sitting up more, you have been rolling over, you have been on your belly, you have been all over the place. Mommy is stretching you and pulling on you and even though you don't always like it the two of you seem to be making some big gains. I wish we could show all your fans a video of you rolling around on the floor because its pretty neat to see just how far you have come in the last week, and even more so in the last month or two. Before long you will be rolling around on your own, I just know it. And I can't forget you sitting up on your own, mommy propped you up in what her and your grandparents call a "pumpkin seat" (I have no idea what it is supposed to be called but I don't think its a pumpkin seat) and you were able to sit there all by yourself and play with your toys on your tray. It was pretty awesome.

What else? Well I have to mention something that I personally have been super excited about since the first time your mommy told me you were coming to see us. The only thing I was adamant about registering for when we went to our first baby store was a baby carrier that would allow me to strap you to my chest and walk around with you looking out at the world. Now after we started seeing some of the problems you were going to face and the tubes that were going to be required to fix those problems I was pretty worried we would never be able to use one of those carriers. But on Wednesday you will never guess what we did.... Oh yeah, we got you strapped to my chest, feeding bag and pump hooked on to my belt and we walked around the house. You loved it, I loved it, mommy loved it. I know that may not seem like a big deal to too many people but I can tell you it was a BIG DEAL to your daddy.

Another big deal that mommy touched on last week is your Ativan. It has been a week since your last dose and (please everyone reading this knock on wood with me here) you haven't seemed to notice at all that it is gone. Mommy and I were super nervous about that one but like you always do you surprised us and breezed through. Next we are hoping to get you off your clonodine patch and that will be the end of the sedative medication. Cross your fingers that your doctor will tell you this week that you can take off your last patch on Thursday.

Which brings me to the last thing of the day. Mommy and I are working to get things together so we can take you to your first doctor's appointment tomorrow. This will be your first of many follow ups as an out patient so both mommy and I want to make sure we are there and have everything ready. It may be nothing more than a doctor's appointment but for you, me, and mommy its a BIG THING. One more step, one more little thing that leads to big things. So here we go buddy, keep up the good work.

We are so proud of you every day Connor. Mommy and Daddy love you.

 - Daddy

Some extras....



Monday, April 22, 2013

Home sweet home. What's that?

Hi Little Man,

It's been a week, seven days since you left the hospital last Tuesday to come to a place that so many people have told you about....Home.  Home is a place that most people feel comfortable and know very well.  For you it's a bit of a different story.  The only home you have known for the first six and a half months of your life has been the hospital.  To top that off mommy and daddy don't exactly have an established home to bring you to because the the insanity of moving from Texas, your early arrival and then our unexpected hospital adventure.  Thankfully Grandma and grandpa have not only opened their home to us but rearranged the vast majority of their house and lives to make a wonderful place for us.  Mommy isn't going to lie she was a little nervous to spring you from the hospital but excited to start the next chapter of our lives.

We have heard stories of babies that have been in the hospital for a long time and not done so well with the transition home.  I imagine it has to be a lot of big changes for a little guy.  As with most big things you have been faced with you took it on like it was nothing.  You were calm and happy on your first car ride home.  When we walked into Grandma and Grandpa's house (which was beautifully decorated by mommy's friend Julie) you were nothing but smiles.  You behaved like a good little boy all afternoon playing with grandma and grandpa while mommy and daddy signed paperwork and got things organized.  Then as things started to settle down mommy sat down next to you and realized something didn't look right.  Your feeding tube was hanging down further than usual and so mommy lifted up your shirt to inspect things.  Unfortunately your feeding tube was almost all the way out.  

So within a matter of a few hours you were back in the car and heading toward Children's Hospital.  There's one thing that's for certain, you don't travel light.  Luckily your doctor called ahead and we didn't have to wait in the ER so we could head straight to radiology.  The next hour or so wasn't the most fun for any of us.  The doctors had a pretty hard time getting the tube back where they needed it and despite the fact that you hadn't had a nap all day you were amazingly good.  Mommy and daddy are so thankful that we have such a tough little boy.  Thankfully the tube was back in and we didn't have to spend the night in the hospital.  Back home we headed.  Let's not make these late night runs a habit.   We need that tube so you can get your milkshakes and medicine.

The rest of the week has been filled with settling into your new room, your new house, and your new routine.  You have adapted very well to your new surroundings.  We have played not only in your super cool room but in the family room and even ventured into the kitchen while we all eat dinner.  When you move from room to room it kind of looks like a parade traveling through the house.  It's not the easiest thing but mommy and daddy won't let that stop us.  I have a feeling that is how a lot of things in your life are going to be, not so easy but worth the work.  As far as a schedule we haven't exactly gotten that down to a science yet but who really cares.  The important thing is that you sleep pretty well at night and we have all day to get the rest of our work done.

You have had a few visitors already and made it home just in time to celebrate your girlfriend Auntie Beth's birthday.  Although she seemed to like her present I think she was much more excited about cuddling with you on the couch.  There is a new person that has started coming to visit you each night.  Her name is Stacey and she is your nurse.  You haven't seen all that much of her because you are usually asleep when she gets here and still sleeping when she leaves in the morning but mommy and daddy are extremely thankful that she is here.  Because we know that she is taking good care of you at night we have been able to get a little rest the past few nights which is much needed.  Please be nice to her buddy because we need her to stick around.

We do need to ask all of your fans to say an extra prayer or two for you in the coming days.  It appears that you are either teething or working on your first cold.  You have been a little fussy and super snotty with a few low grade temperatures over the past two days.  We've been in touch with your doctor and keeping a close eye on everything but our main goal is to get you through this without returning to the hospital.  I know a cold sounds like no big deal but as one of the ICU doctor's said a long time ago "Connor's first cold will be a big deal, a life event."  We are hoping to prove him wrong and breeze through this.  Right now it seems we're on the upswing so rest up little buddy so we can stay home and play some more.

Connor we love you so much and can't express how happy we are to have you home with us.

Love,
Mommy

P.S.  Yesterday was your last dose of Ativan.  Yes! Another medicine off the list.