(Warning: This is a long post.)
For a long time, my blog was my baby. I was proud of what I had written and
the way it allowed others to connect to me. To have a peak into my crazy life without having to get
messy themselves. And then my life
changed in what feels like a single lunch date with a friend. After that, I began to travel a road
that I didn’t feel comfortable sharing far and wide. You see, I was fine at laughing at myself and laughing at my
kids’ antics. Sharing my own
insecurities and failures. All of
that was fair game as far as I was concerned. But real issues for my very real kids? I wasn't so sure the world wide web was the place to be airing that particular bag of laundry. But during a God-ordained lunch almost 3 years ago,
pieces started falling into place in the puzzle that was my son Jake’s
development…and everything changed.
It seems like it was right around the time that Jake was
born that autism became a major buzzword.
What is it? What causes it? Who has it? Celebrities began to write books about their own children’s
struggles. Fingers were pointed at
vaccinations and doctors. There
was lots of scrambling trying to figure out what was going on and what could be
done to fix it. I looked at my
gorgeous baby boy and prayed to God that he would be spared from this. I scrutinized his development, his
interactions. I talked to another
young mom, a former teacher, who had studied and dealt with autism. She assured me I had nothing to worry
about. My loveable son was in no
danger.
So, when Jake took longer to babble then most babies do, I
reminded myself that it wasn’t a contest.
When he finally started to babble at 9 months I breathed a sigh of
relief and chided myself for being so silly. And then other toddlers his age began to speak their first
words. I waited. And waited. And waited for Jake to also
begin using words. As his ear
infections raged on, I figured all that fluid must be preventing him from
hearing properly, thus stunting his speech growth. Finally, after many more months he could say a
word or two and I again reminded myself all kids develop at different
rates. After all, Jake was SO
physically capable. It wasn’t that
he couldn’t talk, it was that he had too much adventure in him to bother with
words.
I mentioned my concern, finally, to Jake’s pediatrician and she
referred us to audiology for a hearing test and to ENT to discuss tubes. After his tubes went in I thought,
“This is it! Finally!! We are going to have a new kid on our hands. One who talks in complete sentences and
expresses his desires and wants using his vocabulary!” Ah, but alas, it was not so. And a referral was made to
Tennessee Early Intervention Services.
People came to test him, he qualified for speech therapy and again I
felt that all was going to be right with the world. He just needed a bit of extra help. What else could I expect from a kid who
hadn’t heard properly for so much of his life.
Jake made great strides with speech therapy. It was exciting to see him put together
a three word phrase (More fish, please!) as his therapist played silly games
with him. When Jake aged out of
the program at 3 years old, my parents were so impressed with his progress they
(and my grandparents) paid to keep him in therapy. I kept waiting for it to all fall into place now that he could
speak. I thought play date offers
would start rolling in and Jake would be the big man on the preschool
campus. I waited. And waited.
Shortly after we moved here, I had my friend Lisa over for
lunch one day after our boys finished preschool. We sat and got to know one another and she shared that her son
was on the autistic spectrum. As
she began to share more, I felt like the room started to spin. Jake was one room over eating lunch
under the dining room table so that no one would look at him. I looked at Lisa and asked her, “How did
you know?” And then the tears started to fall.
That night, I called Ryan in Texas and told him we needed to
have Jake evaluated. That I
thought he may be autistic. Or
have Aspergers. Or PDD-NOS. Or SPD. Of ADHD. Or…..any of the other things I’d read
in a frenzy during that afternoon’s naptime. My husband was, as usual, calm and reassuring. But this time I knew that I needed to
keep some of my frenzy alive. I
needed to not be soothed into inertia but have just enough fear in me to keep
my feet to the fire.
Thus began a very long process of appointments and referrals
and appointments and phone calls and incorrect referrals and more phone calls
and tears and insurance issues and…I could go on but let’s be honest, you want
me to stop. Many months
later, we met with the developmental pediatrician to finally get our
answer. We had been back and
forth to Chapel Hill many times by this point. Had current and former teachers, as well as ourselves, answer pages of questions. Jake had been through evaluations and
the near constant scrutiny of his parents (ok, parent, it was mostly me!). And finally we were ready for an
answer. By this point I knew that
there would be an answer. I knew
it wouldn’t be a smile and, “There is nothing wrong with your fine son.” The more we delved into our concerns
and talked through them with the team of professionals, the more we could see
that many somethings were not right.
And so it was with a mixture of sadness and relief that the Dr. told us
that she was going to give Jake the diagnosis of having an Autism Spectrum Disorder.
It wasn’t an easy call for her, we came to find out. She had really struggled with whether
or not it would be more or less beneficial to Jake to stick him with this
label. On one hand, he would,
obviously, have a label (duh), but, on the other hand, this label would qualify
him for an IEP (Individualized Education Plan) from school and open up a whole
world of services to him. In
the end, she felt that the benefits outweighed the risks and we agreed with
her.
The Spectrum is really vast. Two kids can both be labeled as “on the spectrum” and yet
have almost no overlap in delays, issues, sensitivities, etc. Two years later, I can say that I’m
grateful she carefully weighed the decision and made the call to label.
There is really
no end to stories to share.
Some are for laughter, some are stories of answered prayers and others
are, in some way, a plea for more understanding and awareness for the children
who don’t fit the mold.
If you think you have room in your heart for a little more empathy and
understanding, then please keep going on this journey with me. I don’t have lots of (any!) answers but
I have lots of stories, hopes, fears, answered prayers, lessons learned, and
love for my dear boy.
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