I sit, motionless, still reeling from the words I had just
heard. The words ache in my ears. The tears don’t come just yet, but they are
beginning to burn fiercely as they well up. Then, like a flood gate they flow,
almost unending for days on end…
The words, you ask? Confirmation. Science in its boldest
form. Trisomy 21. Three copies of the 21st chromosome. DOWN
SYNDROME. There they were again…this time in print, so I could torture myself by
reading them over and over and over.
I had been holding on to hope for nearly two weeks. This hope,
resembling a strong woven rope, was holding me up, helping me through each day.
Hope that our new little baby didn’t have to live under the label that doctors
and nurses casually slapped on him when he was born. The karyotype blood test
had been performed on Reece in the hospital when he was only two days old, but the
results typically took two weeks to come in. Two weeks to stare at him and
convince myself that everyone was wrong. Believing that his almond eyes were
just a unique feature, and the palmar creases in his hands were passed along
from a family member, after all, my grandmother has the same creases and she doesn’t
have Down syndrome.
Our appointment with the pediatrician was on a Monday, a
sweltering, August Monday. It was my actual due date for Reece, but the little
man decided to surprise us two weeks early. This was the day we were going to
get the karyotype blood test results. I dragged that hope into the exam room,
feeling the rough fibers of that rope between my fingers, it was holding me up
just as it had over the last fourteen days. Waiting for the doctor to join us
in the room was beyond nerve wracking and all I could do was pace the floor,
five steps this way and five steps back. We waited, knowing on the other side
of that door were results that would determine the course of this little boy’s
life, our life. Jeff held Reece as I paced and for what seemed like forever, and
we waited.
The door swung open and in walked the doctor holding a crisp
white piece of paper. I took a seat in the lone chair in the room and braced
myself for the news. Without as much as a hello, the doctor said, “Well, we got
the results…and he does have it.” My hope began to unravel faster than I could
hold the rope together until it swiftly dwindled into the smallest of threads,
eventually snapping from the pressure of the blow.
An avalanche of sorrow fell on my shoulders and with that I
began to cry. Seeing my tears, “Oh, I thought you knew?” the doctor callously questioned.
I couldn’t even believe that there could be anything but encouragement coming
from her mouth at a fragile time like this, and I wanted to scream at her “NO!
I didn’t know. I didn’t know he had Down syndrome for sure, but now I guess I
do…don’t I?” But instead, I maintained my composure and asked for some time
alone. The remainder of the appointment is a blur to me, but the reality of
Reece’s diagnosis was painfully clear.
A quiet knock, as not to wake the sleeping baby, who was now
just a few weeks old. In walked a representative from a local Down syndrome
organization, who called to request a visit with us shortly after we received
our heartbreaking news. It took everything within me to accept her invitation
as I was walking through a very dark place and struggling with acceptance. She
was a kind-hearted soul who had a child with Down syndrome of her own. Finally,
someone who really understood what we were going through. She gave us a new
parent welcome basket filled with information and gifts, which I’m embarrassed to
admit, sat in a corner for months before it was even touched. But it wasn’t the
gifts she gave us that stuck with me, it was what she said that turned out to
be the most precious gift of all.
“What you’re feeling isn’t good, isn’t bad, it just…is. And
if I had a magic wand to wave this all away, I wouldn’t even do it, because you
have to experience this heartache, this pain, this sadness to get to a place of
true acceptance.”
There it was. Something I didn’t want to hear at the time,
but now look back and know it was exactly what I needed. It went far beyond the
“I’m sorry” that most people whispered with best intentions when we told them
our news. In my heart, I knew we were not alone. How many parents had already
navigated this path we were beginning to tread?
And now, 19 months into this journey…I can honestly say, if I
had a magic wand to wave it all away, I wouldn’t even do it, because I did need
to experience that heartache, that pain, and that sadness to get to the place
of true acceptance that I find myself in now.
First off, you're a great writer! Second, this was a great post. Having lost a baby I felt much of what you wrote. I know the circumstances are completely different but we both needed to grieve for what was lost for us the life of our son and for you a "normal" life for your son. The woman was giving you permission to grieve and rightly so what a wonderful woman. Seth and I have said before that we'd never wish what we went though on anyone and even now 7 years later we miss him but we wouldn't change what happened because it has made us the parents, spouses, the people that we are today. Very well said! We love you guys and are so excited to see all that God has for your family and for Reece!
ReplyDeleteI love your writing Alissa. It speaks so loud! And I love that you are sharing your life. It's amazing.
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