All,
Everything is going great with Pierce. He did well with the surgery and we were back at home the next day. He is doing fantastic and is moving his tongue around, swallowing with the Passy Muir Value on and also can hear something with the tubes in.
I just cannot post to this as regularly as I would like but I am going to try something new. If you noticed, I have now embedded my Twitter Feed on this page...its on the right.-------------->
Hopefully I can post quick tweets and pictures so that you all can get updates more regularly...that being said, you can tweet right back in the feed...feel free to post something to my feed.
Hope all is well with everyone. We are all great here!
Ben
Friday, February 20, 2015
Friday, January 9, 2015
Today is the day
Alright, so I suck. Sorry about that. I realize that a lot of you keep track of Pierce through this blag and although it was intended to be more regular, once we got out of the NICU, I just kind of let it go by the wayside. I feel as though I primarily update this when we are in the hospital, like we are today. I will attempt to be better about posting here more regularly.
Today we are in the hospital for surgery. Today is the day that he will get tubes in his ears to release the fluid, repair his cleft palate and reverse the tongue lip adhesion. This is a big day for Pierce and also for us. I think that this surgery is going to be great and is going to make a difference in his development. The doctors (aside from one) seem to be a bit more aprehensive; however, I dont really care. I think, these are important surgeries and cannot hurt.
Anyhow, Nicole and I have just finished breakfast after having waited for a couple of hours for him to get into the OR. I will update this after the surgery is finished and let you all know how everything went. I am imagining that it will go swimingly.
In the meantime, check out the photo of Pierce's spralled across Nicole upset and sleeping since we woke him up at 545 am. HA!
We will be in the PICU for a couple of days so I will blog while there. Stay tuned for some additional updates and pictures.
Go Pierce! 
Today we are in the hospital for surgery. Today is the day that he will get tubes in his ears to release the fluid, repair his cleft palate and reverse the tongue lip adhesion. This is a big day for Pierce and also for us. I think that this surgery is going to be great and is going to make a difference in his development. The doctors (aside from one) seem to be a bit more aprehensive; however, I dont really care. I think, these are important surgeries and cannot hurt.
Anyhow, Nicole and I have just finished breakfast after having waited for a couple of hours for him to get into the OR. I will update this after the surgery is finished and let you all know how everything went. I am imagining that it will go swimingly.
In the meantime, check out the photo of Pierce's spralled across Nicole upset and sleeping since we woke him up at 545 am. HA!
We will be in the PICU for a couple of days so I will blog while there. Stay tuned for some additional updates and pictures.
Go Pierce!
Tuesday, July 29, 2014
Heading back to work...
Family and friends,
It has been a solid six weeks since I have even thought about blogging. Sorry to all of you who look at this page regularly, hoping for an update. Even though I have been home I just haven't been into it and so I haven't blogged. I have just been spending time with Pierce, enjoying the last month and a half of my paternity leave and kicking back. Although, let me tell you...I am looking forward to going back to work. Crazy as it may seem, I think the adult interaction in a professional setting is what is really appealing to me. Even though I can get adult interaction with Pierce around it just isn't the same. That and taking care of a kid full time is job in and of itself. It is not property management, but different. It is fulfilling, but different. It is rewarding, but different. Okay...enough about me. I realize that you are on this blog to hear about Pierce so let me get to it.............drum roll please.........
Pierce is doing great!
The end. Take care. I will talk to you all in another six weeks or so.
Haha, just kidding.
Pierce really is doing great. He is growing and thriving. As of yesterday he is 16 lbs, 7 oz and is 25 inches long. He has not grown a cm in the last month and because of that his pediatrician cut back a bit on his food. This is good because since we have complete control over his caloric intake, we can be sure that he does not become a fatty (the pediatricians word, not mine - even though this sounds mean, it really isn't and Pierce's pediatrician is fantastic) and we can make sure that his food increases when he grows. He has greater head control and can almost hold it up on his own, albeit for short periods of time, but he is getting there. He plays with an old Fisher Price spinning pyramid, which he loves. The cause and effect really work for him. He also loves this ball that Nicole got for him. He will put his arm in it and bat all sorts of stuff in his crib. It is hilarious.
We also found out (through an MRI) that he is a good candidate for cochlear implants. The ENT doctor said that the anatomy is intact and that he is confident that Pierce will have usable hearing (not just ambient noise recognition) which is fantastic news. I was on the fence about having him go through another surgery if all that he would hear would be ambient noise. This info is great though. The plan is to have that surgery at one year of age. Now, before he can get one of them implanted at one year of age, he has to have tubes put in his ears to drain the fluid so that they can be all dried out an perfect before they stick a wire in through behind his ear and in his cochlea. We don't need any more infections after all.
When they go to place the tubes, the plan is to have his soft cleft palate repaired and remove the tongue-lip adhesion. This is all great news. Since he has the trach (which is a secure airway) we don't need his tongue adhered there any more. This way he will get additional movement from his tongue and hopefully this will help him swallow food. We have been trying food in his mouth and he has some swallows, but he aspirates a decent amount of the food and I am caught for the rest of the day suctioning out sweet potatoes or peaches or whatever out of his trach. It sucks. Hopefully this will help. You try it....take the tip of your tongue, press it against the inside of your bottom lip and then without removing it, attempt to swallow...not so easy is it? Imagine how it would be for an infant who is just learning how to swallow and has muscle weakness in his upper body.
And yes, he has seemed to have found his swallow...and his gag reflex. Both awesome! Yay Pierce!
So the biggest thing that we found out, happened after his first optometry appointment. Nicole always had a suspicion that he could not move his eyes side to side (they actually go in a big V pattern...crossed eyes when looking down and the opposite when looking up but normal when looking straight ahead). This was confirmed by the optometrist. This information gave us a new underlying diagnosis. Pierce has Moebius Syndrome. It is likely that he does not even have Pierre Robin Sequence as all of those symptoms are common in Moebius Syndrome.
To find out more about Moebius Syndrome, please visit http://www.moebiussyndrome.com. This is the website to the Moebius Syndrome Foundation website. They are the foremost experts on this syndrome. Or you can keep reading and I will give you a quick rundown.
Moebius Syndrome is a rare neurological disorder which effects the 6th and 7th cranial nerves primarily and sometimes others. The cause is unknown, be it environmental, genetic, random or a combination; however, researchers believe that it happens between 4-6 weeks gestation...long before a lot of people know that they are pregnant. In many people the 6th and 7th cranial nerves are paralyzed or completely missing. In Pierce's case they are missing. The most recent statistic is that Moebius effects 1 in 1,000,000 people. Often people can go their entire lives without ever meeting someone who has Moebius. The most obvious in folks with Moebius is that they cannot move their face. Their faces are basically frozen. Folks with Moebius can also not move their eyes laterally. Those are the two main parts of Moebius. Other symptoms may include:
Overall, this is positive news but upsetting at the same time. Even though it could be worse, it isn't and we are thankful that it is what it is.
Pierce was also recently accepted into the Kendall Demonstration School which is part of Gallaudet University. It is a school for the deaf and hard of hearing and he starts in September. It will be two days a week for about four hours a day. It will be awesome for him.
To end on a high note, my mom and grandma came out to visit. We had a GREAT time. Four generations in one household under one roof. It was fantastic. We talked and played with Pierce and had a grand old time.
That's all for right now. Now enjoy some pictures. :) 
It has been a solid six weeks since I have even thought about blogging. Sorry to all of you who look at this page regularly, hoping for an update. Even though I have been home I just haven't been into it and so I haven't blogged. I have just been spending time with Pierce, enjoying the last month and a half of my paternity leave and kicking back. Although, let me tell you...I am looking forward to going back to work. Crazy as it may seem, I think the adult interaction in a professional setting is what is really appealing to me. Even though I can get adult interaction with Pierce around it just isn't the same. That and taking care of a kid full time is job in and of itself. It is not property management, but different. It is fulfilling, but different. It is rewarding, but different. Okay...enough about me. I realize that you are on this blog to hear about Pierce so let me get to it.............drum roll please.........
Pierce is doing great!
The end. Take care. I will talk to you all in another six weeks or so.
Haha, just kidding.
Pierce really is doing great. He is growing and thriving. As of yesterday he is 16 lbs, 7 oz and is 25 inches long. He has not grown a cm in the last month and because of that his pediatrician cut back a bit on his food. This is good because since we have complete control over his caloric intake, we can be sure that he does not become a fatty (the pediatricians word, not mine - even though this sounds mean, it really isn't and Pierce's pediatrician is fantastic) and we can make sure that his food increases when he grows. He has greater head control and can almost hold it up on his own, albeit for short periods of time, but he is getting there. He plays with an old Fisher Price spinning pyramid, which he loves. The cause and effect really work for him. He also loves this ball that Nicole got for him. He will put his arm in it and bat all sorts of stuff in his crib. It is hilarious.
We also found out (through an MRI) that he is a good candidate for cochlear implants. The ENT doctor said that the anatomy is intact and that he is confident that Pierce will have usable hearing (not just ambient noise recognition) which is fantastic news. I was on the fence about having him go through another surgery if all that he would hear would be ambient noise. This info is great though. The plan is to have that surgery at one year of age. Now, before he can get one of them implanted at one year of age, he has to have tubes put in his ears to drain the fluid so that they can be all dried out an perfect before they stick a wire in through behind his ear and in his cochlea. We don't need any more infections after all.
When they go to place the tubes, the plan is to have his soft cleft palate repaired and remove the tongue-lip adhesion. This is all great news. Since he has the trach (which is a secure airway) we don't need his tongue adhered there any more. This way he will get additional movement from his tongue and hopefully this will help him swallow food. We have been trying food in his mouth and he has some swallows, but he aspirates a decent amount of the food and I am caught for the rest of the day suctioning out sweet potatoes or peaches or whatever out of his trach. It sucks. Hopefully this will help. You try it....take the tip of your tongue, press it against the inside of your bottom lip and then without removing it, attempt to swallow...not so easy is it? Imagine how it would be for an infant who is just learning how to swallow and has muscle weakness in his upper body.
And yes, he has seemed to have found his swallow...and his gag reflex. Both awesome! Yay Pierce!
So the biggest thing that we found out, happened after his first optometry appointment. Nicole always had a suspicion that he could not move his eyes side to side (they actually go in a big V pattern...crossed eyes when looking down and the opposite when looking up but normal when looking straight ahead). This was confirmed by the optometrist. This information gave us a new underlying diagnosis. Pierce has Moebius Syndrome. It is likely that he does not even have Pierre Robin Sequence as all of those symptoms are common in Moebius Syndrome.
To find out more about Moebius Syndrome, please visit http://www.moebiussyndrome.com. This is the website to the Moebius Syndrome Foundation website. They are the foremost experts on this syndrome. Or you can keep reading and I will give you a quick rundown.
Moebius Syndrome is a rare neurological disorder which effects the 6th and 7th cranial nerves primarily and sometimes others. The cause is unknown, be it environmental, genetic, random or a combination; however, researchers believe that it happens between 4-6 weeks gestation...long before a lot of people know that they are pregnant. In many people the 6th and 7th cranial nerves are paralyzed or completely missing. In Pierce's case they are missing. The most recent statistic is that Moebius effects 1 in 1,000,000 people. Often people can go their entire lives without ever meeting someone who has Moebius. The most obvious in folks with Moebius is that they cannot move their face. Their faces are basically frozen. Folks with Moebius can also not move their eyes laterally. Those are the two main parts of Moebius. Other symptoms may include:
- Lack of facial expression; inability to smile
- Feeding, swallowing and choking problems
- Keeping head back to swallow
- Eye sensitivity due to inability to squint
- Motor delays due to upper body weakness
- Absence of lateral eye movement
- Absence of blinking
- Strabismus (crossed eyes)
- Drooling
- High palate
- Short or deformed tongue
- Limited movement of tongue
- Submucous cleft palate
- Dental problems
- Hearing impairment
- Articulation / speech disorders
- Minor mid-line anomalies
- Club feet
- Hand/feet deformities
Overall, this is positive news but upsetting at the same time. Even though it could be worse, it isn't and we are thankful that it is what it is.
Pierce was also recently accepted into the Kendall Demonstration School which is part of Gallaudet University. It is a school for the deaf and hard of hearing and he starts in September. It will be two days a week for about four hours a day. It will be awesome for him.
To end on a high note, my mom and grandma came out to visit. We had a GREAT time. Four generations in one household under one roof. It was fantastic. We talked and played with Pierce and had a grand old time.
That's all for right now. Now enjoy some pictures. :)
Wednesday, June 18, 2014
Father's day? Birthday? Which is it?
This past Sunday the 15th was my first father's day. It was also my birthday so it was pretty special. Pierce and Nicole put together a great day. First there was a breakfast egg sandwich and presents. From there, we loaded up and took off to one of the local driving ranges which had miniature golf. We had a blast. It was hot, but not humid thank goodness. After that, we hit some balls in the batting cages. I tried curve and fast balls but didn't hit any. Sad really. But the slow pitch softball I was able to hit some of them. After that, it was off to Chinese food with some folks from the neighborhood. This Chinese food that was recommended to us was great....a little ghetto being attached to a Days Inn, but nonetheless great food. From there, back to the house where I invited some of the local neighborhood dads to the house for bourbon and cigars. Then to bed. What a great day. Check out some of the pictures.
Sunday, June 1, 2014
What a weekend
So, this weekend was one busy weekend. I decided that painting the fence would be a good idea now before it gets too hot. It had been beautiful and perfect painting weather, so I got one coat on the fence and it looks rather good, if I don't say so myself. Below is a before and after picture.
Nicole decided to break out the kid carrier. We found out a way to attach his pulse ox to the back of the carpet so that she could walk around and so while carrying him she watered the new trees that she planted last weekend. She planted a golden weeping willow and a Carolina silver bell tree. They are great additions to our yard! See below for Pierce hitching a ride on Nicole!
Sunday, May 18, 2014
Thursday, May 15, 2014
Where do fingers go? In a mouth of course!
Look! He is putting his fingers in his mouth. Nicole thinks that he might be teething. This is really the first time that I have seen him definitively put his fingers in his mouth and kept them there for any extended period of time. How cool!
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