What If I Go To Sleep And Don’t Wake Up?

Chase settled a little further into his pillow as I tucked the sheets up under his chin, just the way he liked it. He had been laughing a second earlier and it suddenly changed to a whimper. “I’m scared . . .”

I tousled the fuzzy hair on his smooth head, “It’s going to be okay, sweet boy.”

He twisted slightly in the sheets as if trying to physically escape a thought. “But Mom, what if I go to sleep and I don’t wake up?”

I hugged him close and promised him that wouldn’t happen – not because I knew it to be true, but because I desperately prayed it so. How the old soul questions from a young body twist at my heart and mind.

It takes four people to hold and distract Chase while the needle is placed in his arm.
It takes four people to hold and distract Chase while the needle is placed in his arm.

Twelve too short hours later, after fourteen hours of fasting and four attempts to place an IV in his under-hydrated veins, he fought the medication as it sought to take hold, pulling his head off the hospital bed to draw breath against the impending sleep even to the point that he nearly choked. His eyes closed and he fought them open once again. His voice was a hushed whisper as if even opening his lips to form words took too much energy. “Mom, I’m going to miss you. Will you come back to me?” The fear in his eyes was still visible in the blank glaze of the pre-anesthesia prescriptions.  And then his chest heaved in a gigantic sigh, and he surrendered.  And I stood in the bay next to Bob, watching nurses and doctors prepare to load his small body into the colossal machine until the automated entrance door closed, separating all of us once again.

We don't like needles . . .
We don’t like needles . . .

Yet another MRI . . .

Today marked Chase’s first MRI in four months and the first one since his diagnosis that I haven’t posted about before it occurred. It was traumatic as it always is and for a moment after the holidays and the busyness and burnout, I lost the ability and desire to put it into words. At some point, it feels like we run out of new ways to say “this is hard” and “please pray”. Every time he passes out and we’re left standing in a room, every last time we say goodbye, it tears at my heart and the weeping soul cry of it all is that we weren’t meant for these kind of things.

It’s hard now, and it’ll probably be equally difficult when we do it all again in three or four months or possibly sooner with an impending eye surgery. And wow, is my weakness and lack of faith on the surface in these moments when I stand separated from Chase and consider doing it all again. We never, ever outgrow the need for moment by moment grace, no matter the circumstance.

Sleeping off the medicines post-scan. He's awake, but was too tired to respond to anything - even a picture.
Sleeping off the medicines post-scan. He’s awake, but was too tired to respond to anything – even a picture.

Oh, but I’m so thankful to be able to bring you the hard and the good all in one, for within a few hours of the nearly two hour scan and recovery, we met with Chase’s neurosurgeon and learned that preliminary results showed negligible growth in the tumor site. Of course, we wait on the final consensus of the other teams and tumor board, but we are so blessed to share that at this point, Chase is stable

Moment by moment.

Weeping may tarry for the night, but joy comes with the morning. Psalm 30:5b

Post-procedure had Teddy Grahams - the best way to break a fast, of course :)
Post-procedure had Teddy Grahams – the best way to break a fast, of course 🙂

Speaking The Struggle

Good morning! I’m over on the St. Baldrick’s Foundation blog this morning, talking about Chase’s amazing meeting with Rep. Peter Roskam earlier this fall.  Join me to read what the US Congress heard about Chase!

Here, I’ll get you started… click on the link below for the full post:

“Over the years, there have been long days and trying times that I want to get up and shout, “This is so hard!” Times when I want to pull out the soapbox for what affects my family, and talk about the lack of funding for childhood cancer research.

Most days, I don’t shout our struggle because we all have something to shout. We all struggle.

Which makes it all the more precious when someone else steps in to shout it for you.

One September morning, I sat in a school gym. The whole family sat in metal folding chairs forming a small arc against the front wall, while hundreds of children and teachers sat on the floor facing us.

The principal stood to welcome everyone in her beautiful red shoes. As she spoke, there was a murmur of activity in the hall outside the gym, and the crowd gathered at the doorway parted for a single, quiet man…”

http://www.stbaldricks.org/blog/post/illinois-representative-peter-roskam-recognizes-ambassador-chase

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Chase’s Story [VIDEO]

Have you ever seen this video of Chase?

If not, I highly recommend it.  And even if so, feel free to watch it again…  We have been so blessed to partner with the St. Baldrick’s Foundation this year and are continually thankful for the platform they give us to share Chase’s story with so many.

-MbM-

[Our deepest gratitude to the incomparable Matthew Lackey for his mad, crazy video skills.  Also, a huge thank you to both Jane Hoppen and Kristen Thies for all they did to put together the finished product and the time spent filming it.]

Three Years And A Letter

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This is my command—be strong and courageous! Do not be afraid or discouraged. For the Lord your God is with you wherever you go. Joshua 1:9

Friday, July 31, 2015

My Chasey-Bear,

How very far you’ve come!  When they first put a name to the giant ball inside your head, the nightmare of it spreading through your skull and down your back, I read that “long term survival” was 3-5 years, and now, here you are: at the three year mark.

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I know you don’t like me to even speak about the hospital on the majority of days and it’s okay, we can mostly play on your terms, but today is different.  This day in your short history, you were on nobody’s terms and only God himself knew what came next as we learned the unfolding: that you would carry a terminal illness with you the rest of your breath here on earth.

I still remember how small you looked in that first ER bed, how confused your eyes were, and how rosy your cheeks got from all the steroids they pumped in as they tried to save you from yourself before the damage became too great.  

I remember holding the oxygen mask to your face and thinking it couldn’t really be happening, and if we were in a movie, that would have been the moment for slow motion and an audible heart beat.  Because sometimes life feels like it’s slowly tearing apart.

We’ve given you over to Jesus more times than I can count and held you close even more time than that.  Yet here you are, still on your journey, standing smack in the middle of your life road, laughing at anything barreling down on you – and how we love you for your fierce, “you-and-what-army” self.

I know these days turned into years have not been easy for you – and I know “not been easy” is a gross understatement.

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None of us know how much further this road continues, but I know if it’s with you – as I’ve known from the first time you kicked inside of me – it will never be dull.  And so we’ll just keep at it as we have tried to all along… in His grace, moment by moment.

All our love, my darling survivor,

Daddy and Mama

Your grace abounds in deepest waters. Your sovereign hand will be my guide.
Where feet may fail and fear surrounds me, You’ve never failed and You won’t start now. So I will call upon Your name and keep my eyes above the waves when oceans rise. My soul will rest in Your embrace, for I am Yours and You are mine.  ~Oceans, Hillsong United

The Two Doors

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“The prognosis for AT/RT has been very poor, although there are some indications that an IRSIII-based therapy can produce long-term survival (60 to 72 months). Two-year survival is less than 20%, average survival postoperatively is 11 months, and doctors often recommend palliative care, especially with younger children because of the poor outcomes.” -Wikipedia on Atypical Teratoid Rhabdoid Tumor

Tomorrow, February 6th, is Chase’s first truly post-treatment MRI.  The first real chemo-is-all-out-of-your-system, three-months-without-a-single-drug-to-guard-against-relapse, have-your-sleep-patterns-changed, why-did-you-forget-that-word, you-fell-twice-yesterday… MRI.

Tomorrow, there will be two doors.  Behind Door #1 is the clear scan and the sigh of relief and the three month wait until next time.  Behind Door #2 is relapse and all the possibilities that it brings.  Writing that thought down leaves me sick to my stomach, but the truth is, we’ve known about Door #2 since the early days of August 2012.  So, even if it comes to that horror, there will likely be few surprises.

People say in mistaken comfort “Yes, but what are the chances…?”  For a parent of a child that only ever had a hairs-breadth percentage of getting cancer and this cancer and surviving this cancer, the chances hold no comfort at all.

The only comfort is in knowing that I am invited to bring my worry to God, and then not worry about it anymore, because He will guard my heart and my mind.  The only comfort is knowing that all of our days were counted and known before we ever breathed, that we were fearfully and wonderfully created, and our very souls cry out with that thought.  The only comfort is knowing that all our pain and suffering is but an earth-moment, and then we’ll stand in the presence of our Savior, understanding the promises and knowing no more pain or sorrow or tears–only closeness to Him forever.

I know those truths.  I believe those truths.  But as I stand in front of these two doors, my heart is still heavy… what now?

BE STILL…  WAIT…  BE SILENT.

“The Lord will fight for you, and you have only to be silent.” Exodus 14:14

Silence?  My make-it-better, make-it-stop, never-give-in heart wants no part of that.  Silence is accepting defeat.  Silence is acquiescing… isn’t it?  Being silent is one of the hardest things for me to do, yet I’m called to do it in this moment.  And as I obey, not speaking becomes speaking.  The quiet becomes loud.  We will watch and see what unfolds as we remember how far we’ve come, and know beyond a shadow of doubt that the same grace that covered all waits always, ahead of us, behind any door.

The doors are in place as they always have been and will be… The right thoughts are known and remembered time and again… and now?

We wait for what He will show us in His time.

We are silent…   Moment by moment.