Friday, July 9, 2010

*there's a beautiful face!


Will's G tube surgery went "perfectly"! He now has a tube free face!


Napping in the holding area before surgery.
After getting the okay from the surgeon, we took out his NG tube for the last time! We made it ceremonial with pictures and celebrating. A nurse came to check on him and said, "Oh his tube is gone." I told her, "We took it out. It was a BIG deal."


 Daddy removed the tape so quickly he didn't even notice.


What is this thing you keep putting in my face Mommy? I'm going to grab it!
The familiar surgery waiting area. It's pretty empty on a Friday afternoon.

Relaxing afterwards in his room. He found something to grab yet again!


His new G tube is surrounded by tape and gauze right now so I'll post a picture of it once it's healed up. They are sending a nurse to our house tomorrow to help take off the bandages. I can't wait to ask questions about how to use the new tube. We have had a lot of messes during the learning process.

We always chuckle about him being marked as a "Fall Risk" since he can't even walk yet.

Here is a little reflection on how Will's time at the hospital has spanned all the seasons:

 Here was fall:
 
This is summer:

Here was winter:
This is summer:

I just noticed how big it looks from the outside:


The tall portion on the left is the doctor's tower where Will sees the cardiologist, GI doc, and the NICU follow-up clinic.

I was trying to kill time with all of these pictures. My excuse for not having any springtime pictures is because that was when he was there for heart surgery and there was no extra time to kill.
 
Back at home!
Beautiful face.

Wednesday, July 7, 2010

*there's a weekend or two of fun

Will's first trip to the lake was Easter weekend. 
Here are a few pictures. He seems so small!
Will's room
Katie sniffing out something to do on the screened porch.
Will and my parents' dog Sissy enjoying the view.
Easter outfit circa 1967

It was Uncle Eric's!
Fast forward to June 19th...Will and I enjoying a book in the glider.



Beautiful lake
Leaving our favorite swimming spot. We'll take Will next summer maybe.
Now for the 4th of July weekend...hanging out in the jumperoo.


He got to meet a lot of relatives for the first time!
Allie Kate showing Will her flag.

 First pics of the little cousins Addison, Will, & Allie Kate:
There was paparazzi everywhere.


If you are a relative that has more pictures from this weekend please send them to me!

Friday, July 2, 2010

*there's an 8 month old!

Happy 8 months of life Will!
Believe it or not, in Will's 8 months he still has not yet reached more days of being at home than in the hospital. In a couple of days we will have passed the 127 total days he spent there. That is more than half of his short little life. On Friday, July 9th Will will go back to the hospital briefly. He is having a G tube put in which requires a minor surgery. Our hope is that he is able to leave in the typical amount of time - 23 hrs. A G tube will let us feed him through a button on the side of his stomach and we can pull the NG tube out of his nose...hopefully forever! Wish him luck and send up lots of prayers please!

Here is the latest:
-Will has had several "play dates" with the kids of my friends. By play date I mean he either stares at them, plays with his toys as usual, cries, or sleeps. He does seem entertained by bigger kids.
-We made our first trip to the grocery store together this week. I was wearing him in a wrap thinking he would go to sleep. I didn't realize he would want to see everything in the store! He was craning his neck to take in all the sights. Also, we had several people stop us to tell me how cute he was. (of course!)
-Each week we have an early intervention teacher, a speech language pathologist, and a physical therapist come to the house to work with him. He's getting practice with a bottle and being more comfortable with us touching his mouth. He's rolling over from his tummy to both the left and right. He has no interest in rolling from his back to his tummy though.
Here he is in action:

Happy floor time on his quilt pallet.
 This is the only way to keep him on his tummy. He can't roll over with a Boppy pillow on both sides! Thanks for loaning it to us Jill!
 
 

We hope everyone has a happy Fourth of July weekend!

Sunday, June 27, 2010

*there's a long awaited visit!

Today was an extra big day in Will's life. The Nashville Chapter of the Baby Will Fan Club (also known as the Niarhos Family) convened for a meeting WITH HIM at HIS HOUSE! Finally!!

Ellen, Mary Fares, & George with Will

These guys were extra excited to meet Will. They have been following his blog and hearing updates on him from their mom since he was born. Despite living really close to the hospital where he spent so much time they haven't been able to visit. Since Will has primarily been an intensive care patient his visitors could only be adults. He was, however, able to get the pictures and cards and crafts they sent! Today he was finally able to receive them in person!

Cards and art from Mary Fares

We will be getting years of fun out of these extra precious finger puppets!

Adorable stuffed animal additions to Will's room:
Will truly enjoyed getting entertained by these three! I don't have any pictures of Ellen's jig dancing, but that proved to be a big hit with getting smiles out of Will.
I am the former babysitter of these kids since the oldest was about 3 and the youngest wasn't even born yet! She is now 10! (The same age as Katie.)

Each of them got a chance to help feed Will. From loading the feeding bag and pushing buttons on the pump...to helping check his NG tube placement with a stethoscope...everyone was a big help.

The gang plus mom Frances helping Will sit on the couch.
Notice how George has one hand behind him. Katie is now an extra big fan of him because he supplied some much needed petting. She even showed him the spot on the couch where she wanted him to sit to provide the best petting situation for herself.

It was an extra fun afternoon of gift getting, dog petting, jig dancing, snack eating, picture taking, reminiscing, and feeding pump teaching! As I write this Will is conked out...happily napping after all the fun!

If you noticed that the word "extra" was used a lot in this post, it is because it has been one of Ellen's favorite words (such as: "If you get the honey mustard with the chicken tenders at J. Alexander's it makes it EXTRA yummy"). When I'm around her I tend to use it extra often. 

Wednesday, June 23, 2010

*there's a feeding explanation

Here is an explanation about Will's feeding. I share this partly in case others want to understand but also because we're going to want to read this one day to see how far we've come.

To summarize: Will has oral aversion. This means he associates swallowing with negative stimuli. A severe oral aversion can sometimes mean that they won't allow anything to touch their face or enter their mouth and they could cry at the sight of food or a bottle. Will's is not that severe. He will take a pacifier when he is tired, he puts his hands and toys in his mouth, and he will also swallow some of his medicine. In the past if I let him get really, really hungry he would nurse and take small amounts. And when he has gone awhile without eating (after surgery for example) he will forget that it used to hurt when he ate from a bottle so he will eat a little. Until his reflux reminds him that it hurts to swallow. Also Will hasn't experienced hunger much and he doesn't realize that he needs to keep eating to fill his stomach. I don't think he understands hunger or that he has the power and responsibility to make it stop by eating. 

As much as we wish we could just pull his feeding tube out and let him try to figure out eating on his own, we have seen it won't work. We did some trials of things here at home and he just didn't eat enough. If we continued to do that for a day or two Will would become dehydrated. When one is dehydrated they are given an I.V. of fluids. Watching Will get an I.V. is very hard. [I think heart babies tend to have this problem. It's as if he feels the pain of the needle stick and clamps down (so to speak); his blood vessels tighten and the needle can't go in. That's my unscientific description, but I have seen nurses repeatedly try and inevitably I.V. specialists are called in to help. Once I saw the night shift give up on trying to get an I.V. in him so they let the day shift try. When those day shift nurses and specialist tried I heard them say "We'll just let the night shift try". In the meantime he has been poked over and over unsuccessfully and is miserable so I won't be responsible for him having to get an I.V. because I didn't feed him enough.]

 First attempt with cereal. 

It's also important to note that Will is at the bottom of the growth chart. This is expected since he weighed 2 lbs when he was born, but going long periods of time with small amounts of food just isn't a good idea. [The growth chart is the thing that tells you when your child is in the 50th percentile in height, the 75th percentile in head circumference, etc. When you do really poorly on the growth chart you are diagnosed with failure to thrive. Will doesn't have that and we plan to keep it that way.] A baby in Will's situation is at risk for falling off the growth chart altogether. Will isn't in danger of this happening, but his weight gain is only as good as it is because of the amount of calories we put in him every day. If we change that he won't do as well. I am certain that when Will is 2 his size will be at least average, but it just doesn't make sense to not do what we can to help him grow. Withholding food sounds like a good way to get him to eat by himself, but trust me when I say we have seen that it won't work. It would work for you and I, but not for a baby that doesn't understand hunger.

Will had several factors that made it likely that he would develop an oral aversion. 
1) Babies with congenital heart defects often have feeding problems.
2) Prolonged nasogastric feeding (his NG tube) - Will has been fed this way for about 6 months out of his 7 month life.
3) Repeated unpleasant mouth experiences - tape being torn off the skin on his cheeks (ouch!), being intubated with the ventilator tube, gloved fingers checking out his mouth, etc.
4) Reflux - I swallow, food goes in, because of reflux it comes back up my esophagus and burns...I may be little but I know how to make that stop...I just won't swallow again.
 More info on his feeding to come soon.
Note to self: 
don't try to feed the baby and take pictures at the same time
Dog update: As of two weeks ago Katie is now officially jealous of Will. She is demanding that we pet her constantly. She is shamelessly crawling into the laps of strangers requiring that they pet her. But conversely instead of ignoring him like she has all the time, she is actually showing some interest in him. She will snuggle up next to me while he is in my lap. I think when he kicks his foot and it brushes against the fur on her back she feels that suffices as him petting her.


Katie decided the Boppy pillow was the perfect napping spot!

Sunday, June 20, 2010

*there's the father of the year!


"It is not flesh and blood but the heart which makes us fathers." 
Friedrich von Schiller 

Will is such a lucky boy. He has a father with a huge heart. I sometimes look at Will and ask him, "How did we score such a good Daddy for you?"


Visiting Daddy at work on Friday before a weekend at the lake:


Enjoying himself on Kentucky Lake this weekend:
Chris has had a very busy and stressful start to fatherhood. Here's to easier and happier times ahead!