Ten tiny toes...Ribbons and Bows...We marvel at the wonder
as our sweet Tessa grows!
Showing posts with label Impact of Others. Show all posts
Showing posts with label Impact of Others. Show all posts

Tuesday, December 13, 2016

A Picture Captures It All

If the Christmas season is heavy, emotional and overwhelming for you...for whatever reason...I would challenge you to consider this...

Imagine a moment...6 years old...looking up at Santa...unable to speak, unable to whisper in his ear or beg of him to tell you which list you are on, unable to hug his neck or sit proudly on his lap...and yet, you experience the magic of Christmas...

What if you are speechless, at the mercy of his embrace and comfort in the moment of splendor and awe. It's a magical encounter that you find inadequate ability to express the excitement to those around you.

But... as a child of God...the reason for Christmas is the birth of Jesus. It's HIS birthday...the day our Savior came for us. So for a moment, you marvel at the magic of Santa...but you find peace and overwhelming gratitude in the gift that was given and the ultimate sacrifice that was made...for us.

Santa is magical...we all want our 6 year old to experience that awe and wonder...but, Christmas is when Christ was born...a birthday that indicates salvation and freedom.

In this moment...Tessa saw the magic...she found out what list she was on and she spoke her wishes gazing into Santa's eyes. But more than that...she knows the true meaning of Christmas and it's a spiritual magic that can't be matched.


The preciously unpredictable pictures with Santa!!! 
Tessa told Santa with her eyes, she was very convincing 😍 ...
Weston wanted nothing to do with any of it 😒...
and Parker did his thing, holding everything together 😘



A couple of our own pics we got at the Hearts for Hearing Christmas party :)
Love my sweet crew



~Whitney

Wednesday, November 30, 2016

No Wrapping

Tuesday was an unexpected day.  The kind where I just sit back and marvel at how every detail plays such a valuable part in the beauty of God working in my life.

I was talking to my sister about it all and she gave me the perfect words...it was a gift that couldn't be wrapped.  Nothing anyone could give me...the kind of gift that only God can orchestrate.  The kind that changes you in ways you didn't think possible and to depths that are impossible to describe.

I'm still having a hard time processing and verbalizing it all.  I feel like it might only make sense to a few.  But I just know I have to write it down.  I can't let time pass without documenting it...this gift of perspective has the potential of being a profound marker in my life.

We had an appointment with the surgeon that will potentially be performing Tessa's surgery this summer on her hips.  Darin originally met with him back in August for what we thought was just to get updated hip x-rays.  There was lots of infomation relayed at that first appointment and it was important for us to go back together and do a repeat so we could process the information together.  That repeat appointment was Tuesday afternoon.  I was stressed.  I was feeling very uneducated because I didn't have the specific information to research the original recommendations for Tessa.  The only thing I really had time to look up was an alternative surgery approach that I was told about that's offered in Texas.

This is a big decision.  The last big decision we made for Tessa was to get her Cochlear Implants.  And honestly, it was not a hard decision for us.  We knew without a doubt we wanted to give Tessa the very best chance at hearing the world around her and give her the best opportunity for communication.  She was so young...just 1 year old when she got her right CI and 2 when she got her left.  The surgeries went very well and recovery was not bad at all.  This decision facing us now...a preventive surgery on her hips...feels like a very big decision.  A big surgery and a big 6 week recovery.  One day I may look back and realize it wasn't quite as big as it felt...but for now, it's huge.

I took all this stress in with me to the appointment on Tuesday.  I was so nervous.  I knew I was going to be that mom asking the millions of questions until the doctor is blue in the face.  But I knew I had to.  I also had everything ready to get his perspective on the alternative approach offered in TX.  This was my first time meeting this doctor and I knew I had the potential of really frustrating him with all my questions and especially by throwing out another doctor's name and approach (if it did frustrate him, I will never know it, he was very professional in addressing all my questions and concerns)...but I definitely went in there carrying that stress with me.  I definitely complicated the situation...stress, nerves, uneducated-protective-mama...the perfect combination to result in any number of unpredictable/unwanted outcomes ;)

I went in praying for clarity and understanding about the surgery...the specific surgery that was being recommended, so that we could make the best decision for our daughter.
I came out with clarity and understanding about our life with Tessa...a new perspective that I've never had.

In an effort to describe how it all came together, it may sound like I am being negative or judgmental about the surgeon, but I most definitely am not.  I truly believe every detail about that day was exactly as it was meant to be.  We have nothing but respect for the surgeon and couldn't be more grateful for the time he spent with us and the patience he had with me and all of my questions.

Throughout the appointment it felt like the doctor was answering my questions with a hint of annoyance on his face.  I actually expected that...I mean I did go into the appointment with somewhat of a goal to annoy, I mean, to educate myself ;)  In trying to describe it to Darin I said 'it was something about his facial expressions'...I have no idea if the doctor even realized he was making an expression, but it is something I picked up on and plays a huge part in changing my perspective.  If I could define the expression it would be - 'it's not that bad'.  Throughout all of our discussions about Tessa's CP, her high tone, her spasticity, her 4 1/2 non-ambulatory rating, etc. etc....time and time again, I would sense that annoyance on the doctor's face, as if to say 'it's not that bad'.  It was very clear that the doctor had experience with situations much more severe.  At one point I felt inclined to call him out on his annoyance (I didn't actually say that)...but I did say something like "you know, Tessa is all we know, to us, her CP is severe. I have friends that have kiddos with CP, but I'm not hands-on with any of them.  I don't have any comparison of what the day in and day out care is like for any other child with CP, I only know our experience with Tessa and it feels very severe."  I went on to describe specifics about the things that Tessa's body does, because of the CP, that can be so hard for us.  He validated everything I was saying and was very understanding, but still...the expression.

I know I'm exaggerating it all a bit in my head now that I'm on the other side of it, but I just sit and wonder what must have been going thru the doctor's head.  When you have a profession like he does and you see the extent to which kiddos can suffer from the effects of CP, there is no doubt in my mind it changes you.  He does what he does to help improve the quality of life for kiddos that have a rough road.  And he helped me realize that yes, Tessa has a rough road.  And of course, life with her and how CP effects her, is all we know.  But he knows more...he has seen more...he has offered medical intervention as a preventive measure and as a necessary measure...he has seen much rougher roads.

I am so thankful that God allowed me to sense annoyance from the doctor (whether it really existed or not).  It communicated a perspective that we are rarely offered in this life of ours...a perspective that 'it's not that bad'...there are rougher roads.  CP impacts every child differently.  It gets worse over time because there are huge downsides to growth.  Doctors don't have all the answers...so much is a mystery.  There is always hesitation to suggest what will or won't happen.  It's anyone's guess.  Darin and I definitely feel like the experts when it comes to Tessa and her care sometimes.  Maybe this was the perfect storm of having an experience with a brand new doctor and conversation with someone that has never been involved in Tessa's care.  Maybe this was the result of all of my ignorance and annoying questions.  Maybe I sensed annoyance in facial expressions that didn't even exist.  Maybe our limited interaction with other children with CP has created a sense of isolation in this specific realm of Tessa's diagnosis.  WHATEVER it was, whatever it is, I am so thankful to have walked away from something with more clarity and understanding than I could have ever asked for.  I'm so thankful that someone was placed in front of me with boldness in the fact that 'it's not that bad'.  I am so thankful that I went into the appointment the train wreck that I was...because I believe God orchestrated all of these pieces to change my perspective and impact me.

The details are a mess when I try and write them down...but they are put together so perfectly in my head.  Whenever I come back and read this I will know exactly what it meant.  In those moments when I sensed the doctor's indication of annoyance I will remember...'it's not that bad'.

Instead of adding more words to this mess, I will end with these.  I went home Tuesday after the appointment and I loved on Tessa in a whole new way.  This was me fully embracing a change in my perspective.  Tessa deserves my very best, but I am incapable of that for her all the time.  But on this night, I promised her I would try.  I would try harder than I have been trying.  I promised her that I will let God change me in the way He is trying to change me.  I thanked her for what she is teaching me...for her patience as we journey this rough road together.

She knows, I know, 'it's not that bad'.
I believe the best gifts in life, can't be wrapped.  I think we miss them sometimes, but I'm so glad I didn't miss this one.


  

















~Whitney

Wednesday, June 29, 2016

A Gift of Accessibility

This month will mark 10 years of life for us in the great state of Oklahoma!  Needless to say, A LOT has happened for me and Darin in the last 10 years...and recently we've had another big change ~ my in-laws have moved to Oklahoma!

For ten years we have lived here without any family nearby.  In the last six, there have definitely been times that we have felt that void in a very significant way.  In the last week...our trek to see family has involved a mere 10 minute drive on I-40...exit to exit.  It feels amazing and surreal...that seems to describe it best at this point :) 

There's one thing that has been incredibly significant during change in our lives...God always shows up...big-time.  When we are selfishly concerned with trying to adjust and all the tiny little details consume us...time and time again...He has reminded me what the change means for Him.

Today I am overwhelmed with gratitude.


The short back-story is that my in-laws are renting a home for now.  They sold their house very quickly in Kansas, but the timing of finding a new home to purchase didn't pan out quite right.  They have the sweetest connections here in Oklahoma and it has truly been amazing to see their community already rallying around them to help them make this big transition in their lives.  

The first group of pictures below are the ones we took of the rent house the night we went to look at it for my in-laws before they moved here.  Such a cute place...but for us and our need for accessibility...there were going to be some initial-visiting-challenges.

The incline to the front walkway is no joke and while we were able to open the car ramp at the steps...we have to lift Tessa in her wheelchair up the steps at the street and then again up the steps at the front of the house.  It isn't something we considered a huge deal and we knew we could get a ramp for the steps up to the house at some point...but without a ramp and any time you are trying to rig accessibility, you can't help but consider the safety risks for everyone involved.

The front of the house and the doozy steps! ;)

Since we first went to look at it, they have added a beautiful little deck at the back of the house, but these were pictures when they had just barely gotten started on that.


The driveway is under the carport, but since our van ramp opens up on the passenger side, we had to stay at the very end of the driveway in order to get Tessa out...again, not a big deal at all, just something we had to accommodate to


We have made several trips in the last week to visit and it has been enough to prove that a solution to the accessibilty/ramp situation was going to be important.  My father-in-law was already thinking ahead and said he had mentioned it to the landlord to make sure he would be okay with us trying to figure out a solution.  

Well, as of this morning...a solution was in full effect.

Today...
The two gentlemen that work for the landlord on his rent houses showed up bright and early to begin working on a solution...and not just that yall, but a permanent solution!

WHO - DOES - THAT ?!?!?!?!?! 

This is the plan...the path for a permanent ramp.

A ramp that will connect to a brand new concrete driveway where we can pull in our van.


I am absolutely humbled at the compassion, and kindness, and forethought, and sacrifice that people who have never even met Tessa are gifting our family...and they are gifting our family by gifting my in-laws...and this is a rent house folks.....a permanent solution in what could be a temporary situation.  
I am overjoyed and overwhelmed.

I told my father-in-law today ~ 
"It is so very humbling for people to be so willing to go to such great lengths...for someone they have never met!  I have been overwhelmed this morning just thinking about it all...just wondering if they will ever understand what it truly means to our family...for what it means we are able to get out and do...when there is accessibility.  Yes there are usually ways around something inaccessible..but unfortunately they cause levels of exhaustion and defeat at times for me and Darin.  It is such a gift when we can go about things with a level of ease."   


God has showed up big...and through all the adjustments and all the details, once again He has made His purpose very clear.  It is rarely about the specifics of our circumstances or the insignificant details of a change...it's about what God can and will do in and through the hearts of people who love Him.

~Whitney

p.s. We can't wait to see the finished product!!! :)

*Some updates added 7/20/2016*






Wednesday, March 30, 2016

New Drawing Tool!

The sweetest group of 2nd year PT students at OU took on a project to create a modified drawing tool for Tessa! They did an incredible job and delivered the final product to Tessa at Lokomat tonight!  Coloring and walking is some serious-multitasking-business and this girl was a serious champ!
Such a neat experience for all of us!






~Whitney


Monday, November 16, 2015

SJN - 3rd Month Memories!!!

10.20.2015
Playground Friendships!



10.27.2015 
Cowboy Rocker Day 
(Tessa is just in her uniform this day)

10.27.2015
Gearing up for pajama day tomorrow with some fun and adorable pigtails!!



10.28.2015
Pajama Day for Tessa and
Mix-Match Day for Parker
a.m. pic :)

10.28.2015 PJ Day at SJN!

10.29.2015
Tacky Tourist Day
a.m. pic ~ personally I think we nailed it!


 Tessa made a spider hat that day at school :)

SJN Tacky Tourist Day!

 11.9.2015
Having Fun Coloring!


11.10.2015
Painting!

11.10.2015
Sweet friends helping get Tessa down the stairs and back to class from recess :)



11.16.2015
"She had a very good day!"
I'd say so with that precious crooked grin on her face! :)

What another incredible month at SJN full of lots of fun, learning and new experiences!!


~Whitney

Saturday, September 26, 2015

DSACO Festival 2015!

It was a beautiful morning to walk with Hudson's Homies at the DSACO Festival 2015!!

We love the Franks Family: Jason, Eilene, Hudson and Bryson!!
It is always a special time to get together each year to love, support and celebrate one another :)







~Whitney