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Welcome! Welcome!

So, what’s my blog about? A little bit of this, a little bit of that, tons about Jackson and a sprinkle of Spina Bifida awareness. Why? Because that’s our life and we want to share it with you. Hope you enjoy!

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  • He's Here!!!
    So, on Monday Jackson was super active, like rolling, flipping, kicking all day.  It was the weirdest thing.  He had never been that active....

Here's What's Happening in Jackson's World: TLSO and HKAFOs



So, Jax has had his new TLSO and HKAFOs for a couple of months now.  He was fitted for them in November and we picked them up the week before Christmas.  I figured I'd take a moment to reminisce and share how both the fitting and delivery went and also fill you all in on the adjustment appointment and provide an update on how things have been going with them both.  

I've done snippets of info and pictures here and there on Facebook, but wanted to do a comprehensive post for my sanity (and memory!).  Because if I don't chronicle it somewhere, I'm never going to remember.  :)  C'mon, you all know what I'm talking about.  I can barely remember my grocery list.  :P

Our appointment for the fitting lasted a couple of hours.  The Orthotist started with the HKAFOs.  He measured Jax's legs and then did casting on both legs.  Jax was okay with it right up until the 2nd leg and then he'd had about enough.  I, of course, was tons of help - not!  Hey, someone has to take pictures.  Nana helped keep Jax occupied and we found that Jax was a huge fan of the Orthotist's tape measure.  


"And just what do you think you're gonna do with that, mister?"

Getting the first leg casted

Thank goodness for tape measures!

"Cheese!"

The TLSO fitting was a whole other story.  By then, we'd been there in the exam room for at least an hour.  It was getting warm, it was near nap time, food time, get-the-heck-outta-Dodge time.  I thought the new TLSO would be similar to the old one.  The last time, it was made by just using measurements.  This time, though, it was made via a cast.  That's right, people, we had to cast his whole upper torso.  I laugh now, because it took four people to cast one little toddler, but man were we all essential.  Because Jax is unable to stand, one person had to hold him up in a standing position, while another held him up by his torso, while another person held his hands to makes sure he didn't touch the sticky mess and then the Orthotist actually did the casting.  Not a whole lot of pics taken at that point because I was in the trenches doing the work.  


Casting for the TLSO.  Not fun!

It took about a month for the HKAFOs and the TLSO to come in.  We went to pick them up a few days before Christmas.  Talk about an awesome Christmas present, right?  That appointment was a lengthy one as well.  Mostly because Jax needed to try them both on and then then the Orthotist needed to make adjustments.  That, and we needed time for photo ops of the momentous occasion.  It's not every day that your kiddo can stand on his own.  ;)


Happy Jax with his football

Jax and Daddy

Very first time in his HKAFOs!!

Big, Tall Boy!  <3

Getting bored waiting for adjustments (and hungry too - had to resort to eating Jax's cheerios!)

Thank goodness for free wi-fi this time around!

Just chillin' in his new TLSO

Lightning McQueen and Mater were also very helpful in keeping Jax occupied

Watching Doc McStuffins

Peek A Boo!

Little Rock Star
"Look Mom!  I'm standing AND I got Papa's pens!"

It's been a few months since we've picked them up and so far, so good.  We went back a month later for a follow-up with Dr. Sanders and he wanted some adjustments made to the TLSO because it wasn't providing enough correction for the scoliosis.  We also had the orthotist add a strap to the HKAFOs at the foot so Jackson's feet wouldn't pop up like they usually do.  

In the waiting room at Dr. Sanders' office

Our big boy didn't cry during his x-ray.  That's a first for him.  So proud!

Unfortunately his curve is getting worse.  The pic on the left is with the new TLSO (before adjustments were made).  The pic on the right is from November with the old TLSO.  Jax will continue to wear the TLSO and we'll follow up in May to see how he's doing.

Killing time by playing his Bubble Guppies game on his LeapPad

"I can play with the drawers while watching myself in the mirror?  Awesome!!"

The TLSO took a little getting used to but Jackson doesn't mind this one at all especially compared to the first one he had.  Because this one was custom-made via casting, it fits a lot better and isn't as bulky.  He's able to sit up on his own with this one and provides for more flexibility.  He's wearing this one a lot more than the first one.  I'd say we're at about 3/4 of the 23/7 rule which I think is a vast improvement.  There are some days where he takes more breaks and doesn't wear it as much while other days he'll have it on the whole day with only a couple small breaks.  I still haven't mastered the art of diaper-changing while he's got the brace on, but I'm getting there.  ;)

The HKAFOs are going well too.  Right now the focus is on getting him to be more confident while standing in them.  At some point in the future, we'll work towards actually getting him to walk with them, but that's still a ways away.  He wears these a couple times a day for an hour or so each time.  

Bowling while standing in his HKAFOs
Practicing standing while using a walker


Peace out.






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Halloween!!!



It didn't take that long to come up with an idea for Halloween this year.  I had actually thought of it last year, but wasn't exactly sure how to pull it off using Jackson's stroller.  This year though Jackson has a wheelchair, so it was much easier to adapt that.  

Enter, CoolestHomemadeCostumes.com!  They had a great article on how they adapted a wheelchair for a biker costume.  That's right, a biker!  I mean, c'mon, it's only natural that Jax would be a biker at some point for Halloween.  He's already got the gear, he just needed the wheels.  



I showed Jason the website and let him do most of the work.  I'm pretty sure he didn't mind as he got to play with his welder.  ;)  One of our friends graciously donated some bicycles that their kids no longer used.  Jason cut the front off of one of them, rewelded some supports and made a plate at the bottom to fasten it to the foot pedal on Jackson's wheelchair.  I think Jason and his buddy Jason (I know, there are a ton of Jasons in our lives!  lol) had a great time working on this!








We had quite a few Halloween events to attend this year and each time the costume changed just a little bit.  In the end, we ended up adding Jason's tool pouch to the front of it, along with a skull headlight (skull was purchased at Jo Ann Fabrics, Jason painted it and then we put an LED light inside), a bike mirror, and a horn.

We had a lot of fun at each of the functions we attended.  We participated in the Al Sigl Community WalkAbout at EastView Mall which benefited the Al Sigl Center.  The money we raised specifically went towards the Rochester Rehabilitation program.  One of Rochester Rehab's programs is SportsNet, which sponsors the Rochester Rookies.  We decided at the last minute to enter the costume contest and Jackson ended up winning Cutest Male.  He came home with a pretty fun gift basket.  We also met some pretty awesome people - Ms. Wheelchair New York and Dino from Fickle 93.3!  Jackson loved Jessica - he thought her tiara was pretty!



Jackson's prize for winning Cutest Male

Jax with Ms. Wheelchair New York <3

We also went trick or treating at Wegmans with a good friend of ours as well as at my work.  My place of employment is the best place to go trick or treating!  You make out very well there - the cube farm is full of places to stop and get candy.  Plus, they do crafts and have cider and donuts!  It's totally worth the drive up there.  We, er Jackson I mean, really enjoyed all that candy!


Trick or Treating at Wegmans

Trick or Treating at Mommy's Work

And to end our Halloween festivities, we went trick or treating on Halloween in Canandaigua.  







We are already in the planning stages of next year's Halloween costume.  We've got a few ideas floating around.  What do you think Jax should be?



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Pumpkins, Horses and Bowling....Oh My!


Pumpkins, horses and bowling....that pretty much sums up our October.  With the exception of Halloween, of course!

I already posted about our annual trip to the Pumpkin Patch, but that wasn't the end of our pumpkin fun.  



We got an opportunity to visit one of our friends and get some up-close-and-personal time with her horses and visit her cute little produce stand.  Jackson has seen horses before but this time was able to walk right up to them and pet them.  He was a little skiddish at first, but very excited to be around them.  He had fun watching us feed them apples.  We sat him up on one, but he wasn't too fond of that.








I've been thinking about horse therapy and did look into it a little bit.  I contacted a local rehab facility and found out that there wait list is rather large.  I def. think though it's something we may consider when he gets a little older.  It will be great for his core strength!

We also went to the GRSBA bowling party in October.  Jax LOVES to bowl.  However, he HATES to take turns!  LOL.  We had a great time hanging out with our GRSBA family and bowling.  Someone from YNN actually came by to cover the event - and Jax made it on the news!  





Wanted nothing to do with getting an face/hand painting done.  But he did go up and visit with them (all on his own).


Here's a video of the story YNN reported about the bowling event:


There was also a Harvest Party at Jax's preschool.  We went and visited some classrooms, did some craft projects and went down to the gross motor room for some music time.  I was a little worried that Jackson would have some sensitivity to the music, but he really enjoyed it.  He even participated up front during one of the songs.  He had a great time and was upset when it was time to leave each activity.  








All in all, October was a busy, fun month.  We did a lot of fun, family things mixed in a couple of doctor's appointments and birthdays and ended it all on a great note with Halloween.  This year Jax went as a biker!  More on that later......


  
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Another Smith Family Blog


I started this blog as a way to keep family and friends, near and far, up-to-speed on what was going on with Jackson. Jackson was born with Spina Bifida and Hydrocephalus. When he was born, he had to have surgery to close the lesion on his back and then had a follow-up a month later for his shunt placement. My goal was to make sure everyone got an updateon how things were going and what better way to mass-update then the good ole interweb ;) And since everyone isn't on FB (WHAT!?!), I figured that a blog would be the next best thing.


Since then, the blog has morphed into a plethora of stuff ranging from date nights, favorite recipes (okay, haven't posted any recipes yet, but they are in the works), our dog, our house, my awesome hubby, projects from Pinterest that I actually complete, SB awareness and what's going on in Jackson's world. I'll be honest, it's 73% about Jackson and raising a child with SB, at least according to my last calculation. Oh, and pictures. Lots of pictures.


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About Me

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Robin
Gorham, New York, United States
I’m a notorious procrastinator, a Martha Stewart wanna-be (minus the orange jump suit), and I have a high attention to detail, although some people might just consider me a control freak, perfectionist pain-in-the-arse! Oh yeah, and I’m a tad sarcastic. I've been married to my best friend for 5 years and we have one amazing little toddler, Jax. Our other "baby" is a 4 year old Great Dane who thinks he's a lap-dog. All in all, I love my life!
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