Watch the progression of the sweetest grin ever! :)
Whoa! That was fun. :)
I got my eye on you.
So this is the face Jet makes when he is trying to run away from me. lol. He is so funny - it's like he truly thinks if I would just let him go he could take off! He snorts like a bull about to charge too. He makes himself quite the tough guy. Watch out!
A week ago David and I found out about a walk to raise awareness for Spina Bifida in our area! The 1.6mile "Walk n' Roll" as it was called was held yesterday Oct. 10th and it was great! We were so excited we made our own team (rather spur of the moment!) who joined us in our walk and helped us raise over 500$ for the SPAG! We are so blessed to have such great family and friends!
David made t-shirts at school that said J. Crew (for Jet's Crew). Cute huh? :)
Jet is read to go!
The orange shirts were made by the family who introduced Jet to Aubie. :) They said "Team Jet" and had a blue jet on them! Fabulous! And they made a little blue one for Jet too! Thanks Johnsons! We loved having everyone out there. What a good day.
So Mr. J LOVES his bath! LOVES IT! As night time falls and brings out his grumpy...he perks up when we put him in his bath. It's so cute!
He loves to splash.
And make funny faces.
Then look away from mommy like he's not doing anything.
And of course we love to suck the water out of the washcloth.
See that trademark pose again! lol
Now you may think I'm a strange mother, but Jet loves being in the sink. lol. It's true! I took his picture in it to prove it! I put him in it one day so I could run his tubby and he just sat wrapped up and quiet (at an otherwise fussy time). I was curious so the next time he was fussy before bath I did it again...not a peep. Then one evening he was cranky and not in the mood for ANYTHING. David wasn't home yet and I was trying to make dinner... so I put him in the downstairs bathroom sink near the kitchen. I know! I might be crazy but he can't get out and he's so happy there! He won't sit in his bouncy seat or swing or lay under his mobile for more than 5min at a time before he cries - but the sink...that's a whole different story. The sink is his happy place. haha. Well, I can count on 1 hand how many times he has really been in a sink...but I thought I'd capture it just to remember those funny times and my funny, funny baby.
Maybe if I open my EYES really wide it will enable me to open my MOUTH really wide! Now where have I seen this phenomena before?
This towel is almost as delicious as that washcloth!
Wow...my hand is so cool.
My nose itches.
Those lights are so pretty.
I wanna touch it.
I left to put my pj's on and the lights are still there!
Has anyone ever looked so stinkin' cute in a hospital gown?
Jet had a big week of doctor visits last week - first on Tuesday he his 4 month check up at the pediatrician - then on Wednesday we went to his PT at the hospital for a follow up - then on Thursday he his second visit to the Spina Bifida Clinic. WOW! Can you say little trooper? Going through all that back to back was no easy task - but Jet was a jewel as usual. :) He's so friendly and loves taking in everything that he only got fussy when he had to miss his regular naptime at the clinic - that visit began with a 7am wake up and wasn't over until 12:30pm. Jet would start to fall asleep on me only to be woke up by a new doctor coming in to meet him.
So here are his stats: 16.5 pounds (75th percentile) 25 inches (50th percentile) and his head was 44cm (90th percentile! lol.). He's growing right on track for the most part. Our only cause for concern was his head growth was very quick - it jumped from the 50th to the 90th in 2 months- a little too quickly according to the doctors. So we mentioned that to our neurosurgeon when we went to clinc. Our NEW neurosurgeon I must add - Dr. Hudgins is moving to Ohio and we will miss him so much. There is something kind of scary about switching doctors - especially when Dr. Hudgins gave us so much comfort and put us at ease during a very uneasy time. But our new doctor - Dr. Brahma - couldn't have been more friendly and seemed very capable - I felt a very good sense of security talking with him and feel confident that this should be an easy transition. :) Thank you God. All that to say - he ordered another head ultrasound on Jet (I was thankful for that action) and oddly and thankfully it seemed unchanged since August. He was very happy at how cognitively aware and alert Jet was so he wasn't too worried yet. I was very glad to here it looked okay still - but we still didn't have an answer for the quick head growth so we are scheduled for a CT scan in a few weeks.
Please, please pray that everything will be sorted out - our hope is that the fluid will go down or stay the same. If it has increased or the CT shows fluid putting pressure on his brain Jet will have to undergo shunt surgery. We are SO thankful that we have made it this far, but we still hope to never have to cross that bridge. Still, we have a Heavenly Father great support system for whatever comes our way, and in that I find peace.
In every other aspect Jet is a super star! The orthopedist and rehab doctors were very pleased (almost surprised) at how good his feet, hips and legs look and move so far. We once again heard the phrases "He looks great" and "He should walk without to much trouble" and are so happy! Go Buddy Go! What a blessed baby you are! :)
So what's the reason I'm wearing a dress again?
Are you sure I have to wear this?
You will be right here Mommy..right?
I'm going to see HOW many doctors?!
At least I have Aubie.
I was such a good boy - Mommy and Nina took me to Barnes and Noble for a story later on. Good stuff.
We've been having some incredible fall weather here in Kennesaw and we LOVE it!
The air is crisper, the sky is sunnier, the clothes are cozier and our little buddy is snugglier. :) On tuesday night we took Mr. J to his first football game! Nothing says Fall like high school football - and the weather was so nice! We bundled our boy up, drove down to David's school (where he teaches...not attends. :)) and stayed a whole 20 minutes before the blaring band, boisterous crowd and banging bleachers were too much for our little guy. lol. He was too overwhelmed poor thing. So we opted for a cozier, quieter evening at home. But not before we documented the occasion with some family pics.
Jet's Little Longhorn t-shirt showed his budding school spirit. :)
An average of 8 babies every day are born with Spina Bifida or a similar birth defect of the brain and spine. There are over 60 million women in the U.S. who could become pregnant and each one is at risk of having a baby born with Spina Bifida.
A friend of mine with a little girl born with SB posted this on her site. I had no idea that October was SB Awareness month but yay Jet! He has his own month! :) Here is what her post said and I thought it was a good summary for anyone who wants to know more about something that is so close to us:
"Spina bifida is a major birth defect of a baby's spine. It is one of the most common, permanently disabling birth defects in the United States. Spina bifida occurs within the first few weeks of pregnancy, often before a woman knows she is pregnant. It happens when the spine and back bones do not close all the way. When this happens, the spinal cord and back bones do not form as they should. A sac of fluid comes through an opening in the baby's back. Much of the time, part of the spinal cord is in this sac and it is damaged.
Most children born with spina bifida live full lives, though they often have lifelong disabilities and need many surgeries. Some of the problems that a person born with spina bifida might face include:
• Not being able to move lower parts of their body. (Some might need to use crutches, braces, or wheelchairs to get around.) • Loss of bowel and bladder control. (Some might wear protective clothing. Others learn new ways to empty their bladders and bowels.) • Fluid building up and putting pressure on the brain (hydrocephalus), which needs to be fixed with an operation. • Allergy to latex (a created material found in some rubber-type products such as balloons or hospital gloves).
All children born with spina bifida don't have the same needs. Some children have problems that are much more severe than others. Even so, with the right care, most of these children will grow up to lead full and productive lives.
Learn what spina bifida is, how it can be prevented, and where to find resources for those affected."
Our little boy born in May 2009 with Spina Bifida. Now he's our 3 year old miracle-baby turned "monkey-man" who keeps us smiling every day. We are so blessed. So thankful. So in love with our little miracle.
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