Monday, September 26, 2011

No smooth sailing.

We're counting down the days... only 8 more!

Unfortunately, it hasn't been smooth sailing.

Josiah has had pain again the last 2 weeks.
It's not all day, but he does have it almost everyday, and has been waking up again at night;
he's been requesting ibuprofen a few times a day.

We're weary.

But thankful.

Pre Op on Thursday!



















Thursday, September 15, 2011

19 DAYS LEFT!

Our surgery date has been set: October 4th the TSF comes off!

Omygosh I can't wait. I may be more excited than Josiah.

It's been a LONG 3 1/2 months... (86days down + 19 more to go= 105 days with the TSF on).

We're ready for the cast.

Thursday, September 8, 2011

Day 79 (11 weeks, 2 days post op)

We're here waiting for our appointment with Dr. Nelson.
I took these pictures of him with my lap top (I'm getting smarter about what to bring with me to pass the time!)



Look how far to the left it's turned out!
Those are some gnarly pins in his shin... yikes!
Kinda gunky & gross... but that's normal.
The top of his skin is SOOO dry. It feels like an elephant foot... but he REFUSES to let me put lotion on it. It's quite the battle when I force it... He's also never had his toe nails trimmed in 79 days!!!!

His knees look dirty & they probably are... but more than that they're super rough from crawling & "walking" on them.
It NEVER fails, though, that when I am prepared with snacks & ways to pass the time, we get seen quickly. Our appt. was at 3:30. It's now 4:20, and we've already had xrays & are currently in the back-room waiting for Dr. Nelson. Those days I leave the house in a rush & forget everything, we are here 3+ hours.

We're hoping that Dr. Nelson says everything looks good and that we can now start the 30 day count down to getting the frame off. (We are soooooo ready for that!)

I'll update once we get home :)



*******UPDATE ON THE UPDATE**************
Dr. Nelson said Josiah's foot looks great and that we can start the count down to removal!
Woooohoooooo!!!!
The TSF will be coming off the 1st week of October. We should be getting a call to schedule the surgery in a few days.
Praise the Lord! No more turns; the correction has been completed.
Next up... a "walking" cast for 6 weeks to 2 months.

TSF at the beach!



Last week, thanks to the help of my mom, we made it to the beach for the 1st time this summer... TSF and all :)

I carried Josiah from the car to the shore. Thankfully, it wasn't a super long walk, and the sand was not very deep. Seeing as how he's almost 60lbs, I know I won't be able to do this much longer! (My back is definitely stronger than day 1, that's for sure!)


Jo had a good ol' time "swimming"






NOT easy to get set up, but once we were out there, it was good.... also not easy to pack up 3 kids, carry them all the car, de-sand them, strap 'em in and then pack up/de-sand all the "stuff" .... but my mom definitely made it possible, if for nothing else than to keep me from getting arrested by leaving the kids unattended! (but of course, she did much more than that).

So glad that we got at least ONE beach trip this summer!

Monday, August 22, 2011

Day 63- Disappointed & Confused.



We saw Dr. Nelson yesterday (praise God he made it back safely from Haiti and was able to do a lot of admirable work there. He said he operated on at least 20 clubfeet cases! God bless him!)
That's the good news.
Now for the bad news (well, it's not bad, really... just disappointing).
(Before I get to that, I'd just like it noted that we left our house at 3pm and got home at 7:30!
I love Dr. Nelson, but I hate going to see him. Our appointment was at 3:40, and we did not see him until 6:30. It definitely provides an opportunity to practice patience and to model a good attitude to Josiah. Not easy! That said, I feel bad for Dr. Nelson though, too, because HE was there that late! I don't know anyone who works harder than that man).

Anyway, we had gone to the appointment with the mindset that we were done with the turns/correcting and that we would now begin our 30 days of "rest" (with the fixator on) and then the 3rd week of Sept we'd have the fixator replaced with a cast.
After Dr. Nelson looked at Jo's foot & xrays, he said that we needed to do 15 more days of turning to bring the foot up 15 degrees.
I had a suspicion that the foot was not flexed up enough, and I even emailed Dr. Nelson asking him about it last week ... I asked how much Josiah's foot should be flexed because right now it is pretty flat. I was right. Dr. Nelson said foot is currently in "neutral."



If you compare this picture to previous ones, you'll see that the bottom halo is now pretty level, whereas before, the front was angled down. It needs to come up.

(In this last picture, you can see the difference in the shape of his feet, how much "over" the left one is currently stretched, and his (in)ability to put them "flat" on the floor).


Our first prescription of turns (to bring the foot over) was 40 days. We assumed the 2nd prescription of turns (to bring the foot up) would also be 40 days. We were pleasantly surprised last month to see that the 2nd prescription was only 25. Turns out it will now be 40 after all!
I wonder if it should have been 40 all along? Dr. Nelson was leaving for Haiti when he gave us the last one. Maybe it was an oversight? I don't know. I guess it doesn't matter. The only change would have been our perception of "the end." Now instead of being in a cast by the last week of Sept, it will be the middle of October.

It's not the end of the world; just disappointing.

It's like when your 9 months preggo & the doctor pushes your due date back 2 weeks... or when you're running with the finish line in sight, then suddenly it is pushed back another 2 miles.

I think I am more disappointed then Josiah.
I am weary of the TSF and the limitations it puts on our family.
Yes, things could be worse, and I am thankful that this is all we have to deal with...
but I'm still weary of it.

Another thing that kind of bothered me yesterday was a comment Dr. Nelson said referring to the right foot. I was asking him about Josiah's other foot and how soon we'd do anything to it (if we do anything at all). He said it was up to us-- that he could put a TSF on the right when he took it off the left-- but that he'd ideally like for us to wait and see what we think of the left's results--- to see if we think it was worth it.
Worth it?
Doesn't he think it's worth it?

I mentioned that I was already thinking it not wise to do anything immediately to the right for the sake of the left's complete recovery. How could he learn to walk/run and gain flexibility on the left again if the right was now immobile?
He agreed that he'd like to see him running around on the left before doing anything to the right. I asked about Treyton (another patient who is done with his TSF & cast) and about his mobility. The last time I talked to his mom, Treyton's foot was very stiff.
When I brought that up, Dr. Nelson explained that Josiah would always have limited mobility in his feet. This "correction" does not improve mobility (nothing can).
I don't know why I hadn't heard this before.
If not to increase the function of the feet, why did we do this?
Just for appearance? So that the foot is "straight"?

He explained that a normal foot's talus (ankle) is rounded and fits nicely in tibia (leg bone). Clubfeet kids have a flat talus, so the ability to flex the foot up will always be limited. (Something I had never been told before. I'm learning more about clubfeet now than ever. I wish I would have learned these things when Josiah was a baby). I found a couple great sites to help me understand:

Clubfoot Parent's Guide
  • Offers a easy to follow explanation of what a clubfoot is, what bones are effected, and what a normal course of correction looks like.
Anatomy of a normal foot/leg
  • This one helps me understand the anatomy of the foot and the vocab necessary to follow what the doctor says! It offers a 360 degree diagram of the foot and when you hover over different bones, it gives the name.


The 1st site helped me understand that the goal of clubfoot correction is to help the child be able to put his foot flat on the ground. As a baby, it was obvious that something needed to be done or he would not be able to walk on his feet.
Before this surgery, Josiah could walk, but he was not able not put his foot completely flat on the ground. He would put his weight on the outside of the foot instead of squarely on the heel & ball of the foot. You can tell by just looking at the correction we've achieved so far that his foot is much flatter than curved like before. Whether that will change his gait, I guess we will have to see.

The goals of his first operation were clear.
I guess I'm confused as to what the goal of this surgery is besides "straightening" the foot. I thought it would improve his foot's function and now I'm not sure.
I will email Dr. Nelson with these questions.

Friday, August 12, 2011

52 days in...

The 3 strut changes went off without a hitch.
Josiah hardly looked up from his Leapster.
(Thank the Lord!)
He has had NO pain, even after turnings.
He's getting around by crawling & walking on his knees.
He's been swimming and playing a lot on the floor.
Things are SO.MUCH.BETTER.

We only have 2 weeks left of "correction" and 30 days of stasis.

We can see the light!

Wednesday, August 3, 2011

Day 43: Things are going well.



8/3/11 Foot is straight & flat. Looking good.

The skin is shiny & red like that, I think, because of the stretching.
It has been that way almost since the beginning.

Nice stretch over to the left is completed.
Now we've begun dorsal flexion (bringing toes up towards sky).




Josiah has recovered well from the operation he had last week.
He has not needed over-the-counter meds at all since last Friday which is better than he was doing BEFORE the operation. Maybe it feels better now that it's more secure?
At any rate, things are back to normal here and we're hoping that the next 22 days of correction are uneventful.
I'm a tad worried about next Tuesday when we go in to have 3 of the 6 struts changed out.
The first time we had them switched, Josiah screamed in the guy's face for 20 minutes at the top of his lungs. It should not hurt at all. They put stabilizing struts in before removing any so that there is no movement of the halos. Josiah just freaks out at the potential pain and he doesn't like anyone handling his frame or even anything brushing up against his skin.
Dr. Nelson will still be in Haiti, so a colleague will be checking Jo out and the tech will do the strut change as usual.

I've been going a little stir crazy during the week, especially because my husband is away on business. It just makes the days feel long. We all look forward to daddy coming home each day, so it's hard when he doesn't.

My sister came over today and we went to the HOA pool next door to my house. It was so nice and Josiah loves to be in the water. It is definitely a challenge with 3 non-swimmers, but with my sister's & nephew's help, we made it work and everyone had a good time.