Aware of Autism

I skipped the traditional posting on Intergalactic Autism Awareness Day, not because I was taking a bold stand or that I was expecting my abstinence to create even the smallest of ripples across the cosmos. Like so much of my life, it was much simpler than that. I just didn’t know what to say. I still don’t. I’ve never known what to say. I just frequently don’t know how to untangle the joy, anger, guilt, sorrow, pride, love, defeat, success and confusion in order to share my thoughts in a manner that makes sense to anyone other than my wife (who after 20 years has perfected – and mostly accepted – the ability to interpret the various grunts and harumphs relative to the elevation of my eyebrows and make sense of what is going on inside my head).

I saw a tweet come across my Twitter feed that summed up my thoughts exactly. “Having a really hard time writing Autism Awareness Month post today. Feeling crapy (sic) & negative & not wanting to reflect that, but its what is.” Amen, sister.

My daughter is “on the spectrum.” We’ve known there were issues (over and above those which we knew of at birth), and we actually nailed the diagnosis by ourselves several years ago. My wife is an information data-mining machine. She had taken comments from various OT’s and PT’s regarding our daughter, and through exhaustive searches and countless conversations with other parents within the disability community, come to the conclusion that maybe we were looking at something on the autism spectrum, possibly Asperger’s Syndrome. We soon had a printout of characteristics and behaviors associated with Asperger’s from Johns Hopkins. Most of the descriptions fit our daughter to a “T”.

It is just over the past couple of years that we had the “experts” diagnose her. The first was an expensive neuro-specialist that handed us the exact same printout (from Johns Hopkins), saying, “Based on what you are telling me, I would suggest she may have Asperger’s.” Thanks, pal.

Most recently, the UCLA Center for Autism Research and Therapy conducted an evaluation over several hours, and confirmed the diagnosis.

I would rather write about anything other than autism “awareness” today.

Like maybe this year’s Redsox opening the season 0-6. Sure, they’re finding new and inventive ways to give games away, but hey, there are still 156 more regular season games to go, and obviously they’re just getting warmed up to lay waste to the other teams in the American League East. I love baseball because there is always tomorrow.

Like maybe the weather. It was sunny and mid-80’s in our burg-by-the-sea today. A perfect day to slip down the street to the beach and stretch out in the sand, with the methodic pounding of the surf as a soundtrack to pelicans diving for their dinner and porpoises occasionally breaking the surface for a breath of air on their journey to wherever it is that they go.

Or maybe even about our big black dog. The Newfoundland is bitter because I made her stay out on the shaded patio all afternoon. You can just see in her eyes that she’d unleash a “thank-god-mom-is-home-from-the-beach-to-let-me-in-the-house-to-sprawl-across-the-floor-in-my-favorite-napping-place” barrage if only she could speak “human.”

Any trivial subject would suffice. Any subject. But not autism “awareness”.

I’m keenly aware of it. So is my wife. It has been blasting through our lives for the past 11 years.

I’m aware of it and I feel differently about it at different times of the day. I feel every emotion known to mankind about autism on nearly every single day of every single week.

I’m certainly still in the grief cycle, still angry for how it manifests in my beautiful, wonderful daughter. There are other issues she faces, but autism is the driver of the train. I despise the trantrums, the raging that has torn at our family fiber over the years. Clinging to each other by our fingernails as OT’s and PT’s suggested remediation techniques, always followed by my daughter dissolving into yet another meltdown after returning home.

I’m pretty sure the people around us are “aware” that our family is different. We’re the ones with the kiddo with no impulse control, the one that addresses all beings as equal (regardless of age, stature or relation). The small child with the gargantuan vocabulary and encyclopedic interest in Meerkats (or Star Wars, or whatever the object of interest is this particular year).

People are aware we don’t go many places as a family because the sensory stimulation of a trip to the grocery store sets in motion the internal chaos within our daughter that more often than not ends in a screaming, wailing eruption. Church? The same.

Yet I love the times of sanity, when she lets us in. The smiles, the times she will slip her hand into mine as we walk down the street. Watching her play with her brother in the back yard, helping him any way that she can. I love the bedtime routine. Tucking her in every night. Watching her expertly comb a beach, in search of shells, crabs, and any other creature inhabiting the surf zone, tidepools or sand. She loves to do so many things.

Mostly, she’s my daughter, a beautiful little girl, who happens to have the label of autism. I love her. As I learn to support her as best I can. To help her through each day. To help us through each day.

And through it all, I need to be more aware of my daughter’s needs, hopes and dreams. I’d like our families and friends to be more aware that we’re doing the best we can to support and nurture our family, and frequently there isn’t much left in the tank to devote to friendships and extended family. I’d like healthcare professionals to be aware that we need concrete tactics explained in simple english to help my daughter. I’d like the regional center to be aware that supports and services are desperately needed for kids with Asperger’s. I’d like the regional center case worker to be aware that we need her to do her job, because even though we look like we have it together, I want to be sure we’re exploring all the options.

And most of all? I want our daughter to be aware that we love her. Because we do.

Explore posts in the same categories: Asperger's Syndrome, Autism

Tags: , , ,

You can comment below, or link to this permanent URL from your own site.

Leave a Reply

Fill in your details below or click an icon to log in: Logo

You are commenting using your account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s

%d bloggers like this: