Spending any
length of time at the hospital is draining. Here’s the thing, though—most of
the time, it’s not especially emotional. Moments come, of course, where you
feel a swirling dizziness as your life changes before your very eyes. But, most
of the time, we tap our fingers and thumb through books we aren’t reading and
joke with our nurses and wait.
And it’s the waiting that drains.
And it’s the waiting that drains.
It’s the waiting that pulls out the obsessive in me-- and I madly scour old college textbooks and online medical journals and Google for information that might predict the future like a crystal ball.
For six weeks,
I had August 14 circled on our family calendar. (Full disclosure: I’ve had the
calendar turned to August since July 25.) For six weeks, I waited to see what
the doctor would say when he looked down her airway, and I hoped that her
airway might be clear so he could take out her trach.
Of everything, the
trach is the thing that has drastically changed our lives. Suffice it to say—
the words sacrifice and patience have new depth for Lee and me. The biggest
problem with her airway seems to have resolved, but we weren’t sure if there
was anything else that might make it hard for her to breathe without the trach.
Waiting for the nurse to take vitals |
Once we knew
decannulation was a real possibility, we waited expectantly, anxiously,
cautiously. (Full disclosure: I waited anxiously; Lee waited cautiously. He is
made of sterner stuff than I.)
So, we went in Thursday morning and waited to hand our baby to the doctors who would put her under anesthesia and look in her trachea. We waited again, and finally heard that the subglottic region of her trachea looked great and they could put in a smaller trach with the hope of capping it and seeing how well she could breathe around it. I thought, “Hooray! The biggest hurdle to her decannulation is cleared. She should pass the rest of her time here easily and come home without the trach!”
So, we went in Thursday morning and waited to hand our baby to the doctors who would put her under anesthesia and look in her trachea. We waited again, and finally heard that the subglottic region of her trachea looked great and they could put in a smaller trach with the hope of capping it and seeing how well she could breathe around it. I thought, “Hooray! The biggest hurdle to her decannulation is cleared. She should pass the rest of her time here easily and come home without the trach!”
So, we waited for the
doctor to come in and cap the trach. She didn’t tolerate that very well because
even the smallest trach takes up a large percentage of her airway. So, the
doctor decided he would come the next day and try to take out the trach
altogether and see what she could do.
Lee spent the night
in an extraordinarily uncomfortable chair, and Friday morning the doctor came
in again. He tried pulling out the trach, but Kate simply is not ready to
breathe without it yet.
So, we came home
Friday with the trach still in place and instructions to wait until she gets
bigger. (And until RSV/ flu season is over—As Lee put it, decannulation is not
a winter sport.) So, we will try again in March.
In the meantime, we
got a pretty great consolation prize: a Passy-Muir valve! This is a speaking
valve that helps her not only make noise but also practice breathing around the
trach. Because it is a one-way valve, it is sometimes used as a half-way step
between depending on the trach and breathing independently.
The Passy Muir Valve |
And so-- for the first
time since she was 12 days old, we heard her.
With the help of her
Passy-Muir valve, Kate cried and cooed while Lee and I looked at the other in
happy shock. Because we spent six months learning her breathing patterns and
silent facial expressions, her little voice sounded strange and miraculous all
at once.
I often misunderstand
when God says wait. Usually, it feels more like no. And though wise,
well-meaning people tell me that God’s timing is perfect, sometimes it is hard
to believe them.
When I am just
sitting on time, it is hard to see how the wait is good. I am impatient.
Now, however, I have
a tangible reminder each time she makes noise that waiting is not always a
waste of time. It is in the waiting that I grip tightly onto prayer and learn
that my God is sovereign.
And my view of prayer
is shaped by my view of God—as I wait, His throne comes clearer into focus
because I have no choice but to trust.
I know that prayer is
no talisman; its answer no barometer of my “goodness.” I cannot barter with the
God of the Universe to ensure my version of a happy ending. As I deal in turn
with disappointment and delight, I can rest in the truth that whatever comes
will be for the greatest good.
I have seen God as
sovereign King, but He does not sit powerful and aloof. He is Father. The kind
that looks and listens. And even though I sometimes feel mad or ungrateful, I
know He will take me as I am and change me. So as I wait, I talk to Him.
I enter the throne
room with nothing to give.
My King—He says,
“Come anyway.”
He uses the words He
spoke long ago to the prophet Jeremiah: “I know the plans I have for you. Call
to me. Come and pray to me, and I will listen to you.”
And though I am no
prophet, I know that those words are for me. Glory becomes Grace as I come
before the One who needs nothing—and in the waiting I am refined.