Sometimes, as Benjamin's mother, I feel as competent as the
mother of a kid on the spectrum can be: I can predict what situations
and variables of a situation will overstimulate him and cause a
meltdown. I can zero in on those issues, prevent and manage what I can,
be prepared with mints and fidget toys and chewy tubes, explain in advance to Ben what might
happen and how he should respond, place events and activities on our
picture schedule and visual calendar. And it works out. Ben handles
the event successfully, he does not have a meltdown, and we are able to
accomplish the task in public at hand. I breathe a big sigh of relief
and can practically feel my Super Mom cape draped around my shoulders as
it unfurls in the wind.
Its not easy to pull off such a feat
A large portion of my daily life revolves around making preparations to ensure Ben
sleeps, eats, has sufficient down time, has been prepared for situations
and how he should respond, and is as prepared and able to deal with the
world outside of our home as possible. I live and breathe Asperger's
syndrome; at least, it feels that way sometimes. I make the preparations
and do the thinking ahead and the worrying, and I brace myself for
dealing with the fallout in case I am wrong
Because, believe me, sometimes I am wrong. Sometimes I am dead wrong.
Sometimes, I find myself in the middle of Target while my child bites the handle bar of the shopping cart and screams bloody murder because there is not a single male cashier at that store. And then I find myself peeling my screaming, flailing 49 pound child out of that shopping cart and stuffing him into my car and into his car seat restraints while 6 people stand around and stare at me. All while I sweat and get a shooting pain beside my eye. Not one of my finer moments, and ironically, it happened about 45 minutes after an appointment with a child psychiatrist who told me I am doing all the right things except putting him a a weighted compression vest in public situations that might cause distress. I just ordered one, by the way.
Sure,
sometimes, Ben does better than I expected. And I rejoice on the rare
occasions when this occurs. Unfortunately, and more frequently, sometimes I miss
something. I forget something or make the mistake that Ben has moved
past an issue when he hasn't. Sometimes, no matter how hard I try, I
just can't control everything that needs to be controlled. Sometimes,
despite having a large variety of snacks, that kid won't eat anything when he needs to.
Or he won't sleep. Or a place is louder than I thought or a place is
busy when I intentionally went at a time I thought it would not be. Or there are no male cashiers or waiters. Or
something doesn't go as planned And sometimes, just like any other kid,
he is just irritable or in an uncooperative mood in general, which
causes his symptoms to flare even if everything else does happen to go as planned.
And
then there is the meltdown. There is shrieking, hitting of himself,
clawing of his arms or face, kicking, biting, swiping at me or innocent
bystanders (nothing makes me want to melt into the ground with shame
more than when Ben swipes at someone else), throwing or shoving things
off of surfaces. Etcetera. Yes, really, etcetera is necessary here. He is
inconsolable and it is almost impossible to get him to hear me explain
something to him while he is melting. He might melt because he is
overwhelmed or physically in pain, because noises are too loud or people
are too close or he doesn't understand a situation, or there is just a
misunderstanding in general that sends his little stressed-out self over
the edge. Etcetera. But I can't explain those misunderstandings or
even remove him from the offensive stimuli because of that meltdown. It stops us in our tracks and freezes us in a hellish moment that I desperately want to break free of but can't.
So
it's not pretty. It frequently involves me grabbing both hands to
prevent swiping, or carrying him (while I still physically can) to
prevent kicking, and maneuvering my shrieking, flailing, 49 pound six-year-old outside or to a restroom or to the car. While everyone stares
at me, whispers about me, and/or offers unsolicited advice about
parenting and laughs about my horrific failures as a mother.
By
the way, perfect strangers who laugh at me and my child or talk about
us hatefully, just because Ben is screaming in my ear, it does not mean I
can't hear you. And sometimes, secretly, I wish he would kick you. In
the face. Or that I could. ***
Just blogging honestly, people.
This is when I feel
that Super Mom cape being ripped off my shoulders. This is when I feel
like a complete and utter failure as a mom and as a person in general.
And after I get Ben calmed down and back in the car, this is when I put
my head on my steering wheel and sob. Or climb into bed and struggle
to get myself back out of it. And I always feel guilty that Ben had a
meltdown and screamed or swiped at people, that I felt angry at him for
melting despite all my efforts to avoid it, and even that I deep down
secretly wished he had kicked the woman who called him a spoiled little
jerk in the face. It's not Ben's fault he has this syndrome. And I
suppose it's not that woman's fault she's ignorant and narrow. I was too
before I became a 7th grade teacher and had Ben, though I never would
have called anyone's kid a name or laughed at them.
I know it's not my fault. I
know I'm a good mom. I know I'm doing the best I can. I don't need that
kind of reassurance. That's not the problem. The problem is that THIS IS MY LIFE, and sometimes it makes me feel as helpless as Ben's Asperger's
makes him feel. Sometimes, it just doesn't matter how hard I try or how much I know.
Sometimes, I feel an overwhelming urge to avoid going out in public or
taking Ben to new places out of fear of a meltdown. Sometimes, the fear of them is crippling. And sometimes, I just have to vent. I don't need reassurance, just a little grace and understanding from time to time. Sometimes, I handle it gracefully and shrug it off, and that is always my goal, but sometimes I'm that woman crying on her steering wheel or peeling her kid out of the shopping cart and shoving him in the car.
I
love my son. He's sweet, smart, funny, helpful, and precious, and I wouldn't
switch kids with anyone. I'm thankful I have him and I can't imagine not
having him in my life as my child. I love my son.
Asperger's, on the other hand, SUCKS.
***There
are countless people who have not done such things. Many people,
strangers and otherwise, have helped me. Thank you to my family and
friends who help me maneuver Ben or simply understand what's up, and
thank you to the strangers who have retrieved my paper towels and
returned them to my cart or slipped my phone or car keys back into my
purse, thoughtfully, silently, and often without the appropriate
thanks.
You are an amazing mother with patience and knowledge I can't even comprehend! I stand in AWE of you! Please God, help me to be the kind of person to help when I see a meltdown and be supportive. Hang in there, dear Danica!!! YOU are the chosen one and God has GREAT plans for you AND BEN!! Love you!
ReplyDeleteHugs and Prayers. I am the mother of a 12 year old son with aspbergers. When my son was 6 or 7 we had so many of the same struggles. Everyone always told me it will get better as he gets older. I thought then they were crazy and that though we muddled through I would never survive. It does get better. They do find better coping mechanisms. I think 6-9 was the hardest stretch for us but there is light in that tunnel. Being a fantastic mother sometimes just takes empathy and a whole lot of love.
ReplyDeleteThank you both!
ReplyDelete