Tuesday, February 23, 2010
Monday, February 22, 2010
"Normal" is as normal does... right?
As we try to settle back in to our life,
everything feels so similar, almost comfortable...
but somehow surprisingly different...
I guess we are still trying to find a new "normal"...
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But this is about as 'normal' as it gets around here!
STRAPPED tightly into their highchairs,
side-by-side,
giggling at my silly lunch-making antics...
like Peanut Butter & Jelly Peek-a-Boo.
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.These two little stinkers are like two peas in a pod!
B follows his big bro around all day, just starstruck.
Mimicking every motion and gesture. Repeating the inflection of every phrase.
Eager to be on to the newest mischevious adventure.
D eats it up.
Loves to be the center of attention. Loves to be adored.
Such a pair.
Oh, what would I do without the TWO of them!
Saturday, February 20, 2010
B Strong... B Fit... Be One... B THERE!
As we acclimate back into "real life"
and marvel in the joy of just being HOME together,
our wonderful, a-MAZ-ing and completely over-achieving sister, Mindy,
is putting this great event together in our behalf.
{Sigh}
The blessings just seem to have no end.
We are absolutely thankful.
(Thanks, Mind!)
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We are also grateful
that this will provide us with a much-needed opportunity
to thank so many of you for your love and support,
and allow us to throw you a bit of a Thank-You Party!
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So whether you run, or not... please
Come celebrate the gift of life with us
in honor of Bronson's second chance!
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There will be a 5K and a Children's 1 Mile Fun Run.
Both starting at 9 am
Food, Games, Prizes, Raffles, Bounce Houses!
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Register online @:
https://www.active.com/event_detail.cfm?event_id=1839825
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We look forward to seeing you there!
Tuesday, February 16, 2010
Today I am grateful...
For the little pile of fishy cracker crumbs I get to vacuum from beneath the kitchen High Chair...
For the big, slobbery kisses smeared at the bottom of my full-length Bathroom mirror...
For two stinky little bums to change, and a diaper genie I get to empty...
For onesies to bleach... and wash... and fold... and put away for another day's use...
For bottles and sippy cups to empty from the Dishwasher...
For the pudgey, pounding little Fred-Flinstone-feet that toddle to answer our doorbell...
For the kisses blown abundantly to strangers, and to friends alike...
I am thankful for the never-ending chaos...
Grateful for the grimey little smudges on my Television screen...
Delighted to re-roll the potty-paper from half way across the room... yet again....
Appreciative of the wild, little maniacs I am able to chase and tickle to hysteria...
Oh, those contagious little giggles...

How I adore them.
How undeserving, and yet how exultant I am to collect them.
How welcome are those eager little arms, wrapping around their Mommy.
Oh, how very fortunate am I...
Sunday, February 14, 2010
Happy Valentine's Day, Sweets...





Bronson's Miracle
We thank you forever for your prayers and your faith on behalf of our little family. We can not thank you enough for helping us to call down the healing powers of heaven to fix our broken little boy. We know that Bronson lives today because it is Heavenly Father's will that he be allowed to stand as a testimony of His miraculous power . We hope to make the most of this second chance. There are truly no words that can express gratitude of this magnitude. Just joy... Pure joy!
Love- The Staker Family
Friday, February 12, 2010
Undisputed Champion of the World...
Coming home...
Thursday, February 11, 2010
If you'd like to see our sweet boy on TV,
Big Steps Forward...
As if we haven't had enough miracles...
This morning we've made another few big steps toward coming home!
B is walking!
He is playing fetch with his new favorite ball!
(Thanks, Auntie Krista!)
And he is off all oxygen and support and is on only minimal monitoring.
No one can believe it!
It is all smiles here!
Wednesday, February 10, 2010
Poor Little Bobble-head...
Tuesday, February 9, 2010
A few small steps... giant leaps!
"Do As I'm Doing" happy time...
Sweetest smile in the world...back again...
Sorry this is sideways... I am too tired to try to figure out how to rotate it.
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Just tip your head sideways and enjoy! ;)
Words can not express...

Remember that hunch?
HE SMILES AT ME WHEN I TICKLE AND PLAY WITH HIM!
Let us never be afraid to share our testimonies boldly.
Monday, February 8, 2010
Bronson's True Colors...






Wiggle worm...

As soon as it was over, he began to seem tachypneic ( pronounced tah-kip-nic).
That's a big fancy way to say he was breathing really fast and hard,
with a heart rate to match.
He seemed to be pulling in so hard for air. Like breathing through a straw.
Retractions heavy. Head bobbing. Looking exhausted.
They bagged and suctioned him.
I hate that.
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A little after 4, I noticed his tummy looked a little too rounded.
It was unmistakably distended.
I pointed it out to Molly, the Nurse, today.
She agreed.
She called in Cory, the Nurse Practitioner,
and together they decided another NG (Nasal Gastric) Tube was the best course of action.
Using a large syringe, she pulled out over 180 cc of trapped air
and about 50 more cc of stomach fluid. Poor kid.
Once out, it seemed to relieve the pressure and his tummy softened and looked normal again.
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A little after 6, he had his 8th poopy diaper of the day.
As I changed it and weighed it for the nurse, I noticed that his poor bum is looking quite red.
Not just a normal red, but bumpy and fierce.
I knew right away it was yeast from the antibiotics.
Molly called Cory again, and they both concurred.
They wrote up an order for Nyastatin ointment.
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Around 8, they started him on his final SBT for the day.
He was resting so soundly, I wondered if it was really worth bothering him.
The RT assured me that it was worth the exercise
if we want to strengthen his little lungs enough to have a chance at extubation tomorrow.
Alright, already...
Close to my heart...


Saturday, February 6, 2010
Baby Steps...
The big thing to report today is the continuation of his arm movements.
Up and all around and even above his head.
He was awake for much of the day, but still had that blank empty stare that we hate.
{Sigh...}
They did remove his femoral central IV line.
There's our one line out for the day.
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A week ago... right now...
.Waxing and waning...
The one he only twitched just a little bit yesterday.
The one they said might be partially paralyzed due to neurological damage.
The one that was unresponsive during the Neuro-Assessment just earlier this morning.
They say these types of brain injuries can evolve.

he batted my hand away. Cognitively. Several times.
Just like he does at home when he's bugged with my ceaseless primping and polishing.
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I ran out and grabbed the Nurse Practitioner, Kristen.
Dr. Bennett ran in as well.
It was smiles all around the room.
I hate to say I told you so...
But ...then maybe I don't! ;)
Friday, February 5, 2010
Chasing out fear, choosing faith...
{Insert HUGE sigh of relief...}
No visible sign of damage to the brain.
That does not insure that the functionality of all his faculties is intact,
but at least it is not a negative.
At least it is not more BAD news.
Today has been our scariest yet.
And also our most sacred.
What a juxtaposition of emotion...
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I went to bed at about 4:30 Friday morning.
Baby B was resting quietly.
I kissed him goodnight and said a prayer with him at his bedside.
He opened his eyes and our hearts connected.
Spirit to spirit.
For just a brief moment
Good Night, my sweet boy, I said.
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I went to my sleep cell a few hallways away.
Thank you, Savannah, for the electric blanket.
I was warm and slept soundly until about 8:15.
I woke and packed up my bag, pulling it back down the hallway,
greeting the familiar faces along the trek.
Another day here at the PICU.
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As I walked into B's room and met the new Day Nurse, Rowdy,
I was immediately alarmed.
In the bed where I'd left my little boy to heal and rest
lay a glassy-eyed guy with a blank, empty stare.
My stomach dropped...
"So how are we this morning?", I asked cautiously.
Rowdy filled me in on the morning's Neuro Exam.
He'd come on shift to meet Bronson for the first time and had been advised of his exciting progress.
But he'd found him a little sluggish.
Wide awake, but not really alert.
Staring blankly without focusing. Looking right through everyone.
Unresponsive to stimuli.
What had changed in those 3 hours and 45 minutes?
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The Nurse Practitioner was called.
Then the Attending Physician.
Then the Neuro-Trauma Specialist.
We hypothesized about the possible changes and his sudden decline.
No one had any answers.
No, I had seen my boy.
We had seen our boy. We were sure of it.
Others were sure of it.

We may have to wait for an MRI until Monday.
How could we wait until Monday?
No, they could squeeze us in.
We waited the long, drugerous hours until 3:00 pm.
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Our Stake President stopped in to see how we were doing.
He found us worried. Well, terrified. Faltering in our faith. Sick.
Matt gathered himself and they offered Bronson a Priesthood Blessing.
He turned his little body and mind back over to the God who had helped us to create him.
Asking for the faith to discover Heavenly Father's will and the strength to follow it.
To align ours with His.
President Francom counseled and advised. Hugged and encouraged.
They took Bronson down for the MRI.
Matt and I held each other in that empty little hospital room and fell apart in each others' arms. Sobbing and clinging to one another, praying.
Pleading for our son with every ounce of strength we could muster.
Sealing our hearts together.
Like never before.
I can not share the words we spoke with one another.
They are the most precious we have ever shared together.
But as I spoke, I realized that faith can not grow where fear is allowed to dwell.
There is not room in my heart for both.
And so I made a choice.
I must choose faith. Choose to believe. Despite the odds.
No matter how vulnerable and unguarded I let myself become, I will not, I can not fear.
I swallowed hard. Past the unbearable burn in my throat.
And even they admit to seeing miracles every day.
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I know Heavenly Father lives.
I know He loves Bronson and has a plan for his life.
If it is God's will for him to remain with us, he will.
Simple as that.
And with the whole world praying, what have I to fear?
The Lord is bound to answer the prayers of the righteous when they are asked in faith.
And this is the righteous desire of our hearts...
We plea that He will spare our son. Heal his body. Protect his mind.
So that he may live out the rest of this mortal life as a testimony of God's miraculous power.
I can not consider the other option.
There is no other option.
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But I am stronger than I thought I was.
I can do hard things.
Our family can do hard things.
We will accept the will of our loving Father in Heaven because it has never lead us astray.
Why would it now?
We will trust. We will be believing.
We will continue loving and being loved.
And we will press on faithfully, because we are faithful.
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This I know...
Bronson's spirit is untouched. It lies within a broken body I do not know how to fix.
But he is ours. Forever. Come what may.
I am blessed to be his Mommy. Matt to be his Daddy.
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The name Bronson means "Strong one".
The name Micheal means "One who is like God".
It is no coincidence that we chose these names for him.
What a powerful force he is...
Our strong, sweet, wonderful, beautiful boy.
By small and simple things, great things are brought to pass.
And great things have already come to pass.
People who do not pray, are praying.
People who do not believe, are finding hope.
People are reevaluating their faith and priorities.
I am reevaluating my faith and my priorities.
And THAT is the miracle.
He is uniting people across the globe.
Literally.
Teaching the power of prayer. Individually. And how collectively, it multiplies exponentially.
Allowing us an opportunity to practice our faith. And allow it to grow.
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I do not know why our family was chosen to pass through this challenge.
But I do know that God is mindful of each and every one of us.
All of the time.
He reaches out with tender arms of mercy.
Extending his grace until we are filled. Until we are enough.
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