Showing posts with label neck fusion. Show all posts
Showing posts with label neck fusion. Show all posts

Wednesday, December 4, 2013

An update on John...

I'm sorry!  I know this post is HOPELESSLY overdue!  I should have written last week. The only excuse I have is that I have literally been racing from task to task for 8 days straight hardly getting a chance to take a breath.  (What else is new, right?)



John's surgery went SO well. There had been fears that since the MRI they were going off of was quite old, that when they got in there they would need to fuse more vertebrae then anticipated. However, when Dr. Ahuja came out to update me after surgery, he said that it looked better than expected when they opened John up, and the surgery went extremely well. WE SERVE A GREAT GOD!

This was literally the best hospital stay we have had in the past 4 years (which is saying something because John has been hospitalized 6 time since 2009!) Every single nurse, CNA, receptionist, doctor, therapist, security guard we encountered was AWESOME!  They were kind, friendly, helpful. Seriously if you need to go to the hospital, Kenosha Medical Center is the place to go! We were only in the hospital for 28 hours from check-in to discharge.  WE SERVE A GREAT GOD!

John is adhering STRICTLY to all the restrictions the Dr. gave:  no driving, lifting only 8 to 10 pounds, wear the neck brace CONSTANTLY.  For those of you who know him, I'm sure this comes as quite a surprise. John Joseph Kastner following the rules?!?!?!?  Really???  All I can say is:  WE SERVE A GREAT GOD!

Recovery is going EXCEPTIONALLY well! Every day, John gets a little stronger and his pain diminishes a little more. Just 8 days after surgery, and he is already taking less pain medication then he has taken in years!  We were able to attend my family's Thanksgiving celebration just 2 days after surgery, AND we made it to church this past Sunday! We are VERY optimistic about the success of this procedure, and we KNOW it is because:  WE SERVE A GREAT GOD!


For you are great and do marvelous deeds; you alone are God.
Psalm 86:10

Please continue in prayer for us.
*We are praying about John's 12/19 post-op appointment. At that appointment, we NEED the x-ray to reveal bone growth so that the Dr. will clear John to return to work.
*Also pray for me.  This Momma is WIPED OUT!  Monday I dove HEAD FIRST back into my regular schedule:  worked 5 hours, homeschooled, coached cheer, cared for a recovering hubby, an old lady, and a newborn. I am SO far beyond exhausted at this point and IT IS ONLY MONDAY! But don't worry.  I haven't forgotten

WE SERVE A GREAT GOD!

Sunday, November 24, 2013

The things that I know...

My heart is full yet somehow the road by which these feelings typically travel out of my heart is blocked..... clogged.
I'm searching for just the right analogy to explain the raw and unadultered fear,  chaos and tension that is bubbling just under the surface of this calm exterior I'm trying to put forth.
Have you ever read the B book? It's an easy reader we have in our library. Pages and pages of B things are introduced. All balancing precariously on a bear on a ball until at last the tiniest bird lands atop the pile, and CRASH the whole thing comes tumbling down. Maybe that's the word picture I'm searching for.
I'm in the midst of a CRAZY full weekend which ends a VERY busy week. I hosted a brunch this morning,  coached a game after that and rushed to teach Christmas choreography after that all while developing a nasty cold. Tomorrow will bring the teaching of more choreography, prepping for the week and a cabke guy appointment.  Then Monday a FULL day of work,  capped off by cheer practice.   I am holding this all together.... placing my ducks in a row... yet still there is this eerie feeling that one tiny little bird atop my pile and CRASH it will ALL come tumbling down.
So what's a girl to do?  In times of uncertainty...  Facing another grueling mountain... Not feeling up to the climb... well I guess I will just focus on the things that I KNOW:
*my God is in control.... time and time again He has proven this. .. I don't expect this time to be any different.
* my husband is a STRONG and capable man who already triumphed over brain surgery
*my children are deeply rooted and will likely be the ones carrying me through on their rock-solid faith
*my family will rally behind me no matter what comes my way
*God's people will be faithful in prayer and in deed
And most importantly....  the thing I know best without a shadow of a doubt:
*He WILL be glorified through the circumstances of this coming week
Please continue to keep John in your prayers.  We are praying and BELIEVING for a SUCCESSFUL surgery,  a MIRACULOUS recovery,  and many MANY chances to proclaim His goodness,  power and mercy.  Thank you for praying with us.

Thursday, October 3, 2013

Roughing up my heart....

Ugh... I don't even KNOW what to title this post.... *sigh* I guess I'll just figure that out at the end. Here we go:

John is scheduled to have neck fusion surgery the third week of December. For those of you who are thinking, what? who? how? why?  here are the details... the rest of you can skip to the bottom if you want.  Just scroll down until you see the bolded words Well so here we are....

If you've been with us for the duration, then you know that 4 years ago John had to have brain surgery to relieve the symptoms of a chiari malformation. Because of that initial surgery, disk degeneration (which he has always had) is worsening and manifesting in some icky symptoms (he is on week 3 of a CONSTANT headache right now.... he is losing strength and size in his left arm... he has pain radiating from his neck all the way down his arm...) Today they told us that left untreated it could eventually result in him losing all function in his left arm.  [Okay that's pretty scary.]

I believe it was back in July of 2012 that we first started hearing about this idea of neck fusion, and then again this past summer it came up. As this appointment to discuss it again approached we started hearing rumors (which are still as of now unconfirmed) that the lovely Affordable Care Act is going to DECIMATE our current AMAZING insurance benefits and knock us down to what all the rest of you have been dealing with for insurance [not being rude, just saying that we have had FABULOUS health insurance every since John changed jobs.... if the rumors prove to be true that will be a thing of the past come January 2014]....  Sooooo these rumors got us thinking that we might need to just DO THIS before we cannot afford to do it because of our "Affordable Care".... When they told us that part about the possibility of it progressing to the point where he would not even have any use of that arm, we were kinda like, "Okay let's get this puppy on the books!"

Again for those of you who want the details.... the gory details.... keep reading... the squeamish... well you've been warned.

So we have been told that this surgery will be MUCH less invasive, painful, difficult than the last one... [although I have to tell you that back in 2009 I DISTINCTLY remember Dr. Ahuja saying, "This is the best brain surgery to have. If you have to have brain surgery, THIS is the one you want to have because it is the easiest one."  WHATEVER!] apparently because they will go in through the front of his neck, moving his muscles to the side instead of cutting through muscle (like they did in the back of his neck) it should result in a much easier recovery. They will be fusing his C4 through C6 vertebrae together in order to give his nerves room to "live" in there and immediately relieving his pain, weakness in his arm and stopping any further degeneration.  Here's the visual they gave us of what they'll be doing.... that black thing is a titanium doo-hickey (yes that IS I think the technical term... at least as I heard it)... underneath the doo-hickey will be some plastic thingys that replace his degenerated discs.


Well so here we are.... walking down roads... living out scenes... asking for prayers... explaining medical terms we have become too familiar with.... all like we've done in the past....  In the short span of just 8 hours since I found out, I have been through the following phases:

Phase 1: I can do all things through Christ Who strengthens me....

The first introduction of this concept of a second surgery actually happening, left me almost cocky and too assured.... "We can do this!  It's easier than the first time. So much is different. We are different.  This is going to be a walk in the park!"  It was in this phase we told the kids, and they pretty much seemed to take it in stride just like I was.

Phase 2: I can do all things through Christ Who strengthens me....

After we told the kids, John and I laid down to try to get a little rest. I fell SOUNDLY asleep, slept too long and arose late for cheer practice and a bit discombobulated. At this point the realization that we were indeed going to do this AGAIN was hitting me and I was left feeling a bit dazed and confused by the punch that realization walloped. I raced off to practice, forgetting Regan's shoes, forgetting a cup of the coffee I asked Noah to brew for me, and forgetting about a certain female situation which I will provide no more details of in case my brother is reading this blog for he will SHOUT, "FOUL!!! TOO MUCH INFORMATION!!!" (In fact he is probably already shouting that.) I drove to practice kinda forgetting where I was and where I was going for a little bit. I felt as foggy and hazy as the weather around me.

Phase 3:  I can do ALL things through Christ Who strengthens me.

I entered phase 3 as I pulled in the driveway after practice. I sat in the car for several minutes sobbing. "God I know I can do this with you. God don't leave my side for a second these next few months. God I NEED you!" screaming from my soul! My weeping left me in a place of quiet resolution. I can do this again. I can get through ANOTHER surgery. I can watch the man I love endure EXCRUCIATING pain. I can watch my dear babies trying to be strong with terror in their eyes. I can DO this.  And that's when God gave me my analogy.

When the surgical assistant was explaining the surgery to us, he said that at the end of the surgery they will "rough up" the bone (vertebrae) around the fusion site. He said they do this to signal the body, something is hurt here we need to fix it.  Then new bone will grow to "accept" the titanium doo-hickey and strengthen up that area.

God is roughing up my heart right now.  He is signaling my spirit that something is hurt and needs to be fixed. Over the next few days, His Holy Spirit will rush in and build "new bone" on my heart to accept this new situation and incorporate it into my reality and make me STRONGER.

As is typical when I come to you through the words of this blog... we NEED your prayers... for the big... for the little... for the seemingly inconsequential...

John is a little nervous/weirded out by this whole thing. I know he DESPERATELY wants his pain to come to an end but the fear that this won't do it or could even make it worse is assaulting him a little.

Noah seems okay right now, but he is the one ALWAYS hardest hit by John's health issues. #1 because John is TRULY his best friend and #2 because he tries to "step up and be the man" when John is down for the count and that is a tough thing for a 9 then and now almost 14 year old to do.

Details... our dr. is doing surgeries at a different hospital now we don't know if it is covered by our insurance.... we are hoping that the vacation time John has available will be enough to cover his recovery time... this will be happening RIGHT in the middle of cheer season, Christmas, etc... not the best timing in some ways but great timing in other ways.

I will try hard to keep you in the loop, but I expect that you will likely only hear from me when I'm begging for prayer or processing the tangle of emotions I am going through.

Thank you friends for your prayers and for always caring enough to walk with us through the dark times.

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