Tuesday, November 8, 2016

The Road To Acceptance

My boy having fun trick-or-treating in his own way on Halloween.      
            Recently my family and I participated in a local walk to support our friends who have a boy with Down Syndrome.  We went to breakfast before the walk at a restaurant where we go pretty much every Sunday.  Our whole family wore matching shirts that had the child’s picture on the front with the phrase “J- Rocks”.  At first I couldn’t figure out why everyone was looking at me, but then I realized what I was wearing.  It made me understand how it must feel to be stared at every day, simply for having a physical difference.  My son’s disability isn’t as immediately obvious as our friend “J-”, but Ben’s hand flaps, his noise canceling headsets, and his aversion to eye contact show the telltale signs of his autism and sensory processing differences.  Over the years I’ve become immune to the looks and the glances from strangers, some of them curious and others a bit more judgmental.  It’s been a long time sense Ben has had a public meltdown, so it’s been awhile since I really stopped to think about how society views disability and how much my own views on the subject have changed.

My road to accepting Ben’s disability (and disability in general) hasn’t always been easy.  Ben was diagnosed with Autism Spectrum Disorder and Sensory Processing Disorder almost four years ago.  It has taken nearly all of that time for me to feel at ease talking about my child’s learning differences with others and to truly see them as just that- differences.  I no longer feel the sting in the back of my throat when I say the word autism.  It has taken years of research and study for me to come to the conclusion that, while my child’s disability brings very real challenges, it also provides him with very real strengths that come with having a differently wired mind.  

I have written on the topic of acceptance before.  You can read about my feelings on the topic here and here.  My definition of acceptance has evolved over the years as I have learned and grown.  To me, acceptance doesn’t mean that we have to like the hard parts of the disability.  It doesn’t mean that we have to stop trying to make life better for our child.  However, we must remember that we are trying to make life better- for our child.  This is very different than trying to make life easier for us, or life more socially comfortable for us.  To me, acceptance means that we love our child without wanting to try to change him simply for the sake of making him more palatable to society. 

            The line between denial and acceptance can be blurry.   Over the years, I have met many parents who are living in the stage of denial.  They want to pretend that nothing is different about their child because they view normalcy as the goal.   The view their child through the lens of the hopes and dreams that they have held since their child has born- the vision of the child they expected to have rather than the child in front of them.  They have been influenced by society’s insidious message that those with disabilities are objects to be pitied, or individuals who have a lower self-worth than others.  While they may acknowledge their child’s disability, they see their child as a project to be fixed.  When their child does something that is outside the realm of “normal”, they feel embarrassment or shame and actively try to suppress these things.  I don't judge those who are in the denial stage.  I was there once too.

            It may appear to the casual observer that those who accept their child’s differences no longer care about their child’s needs, but this simply isn’t true.  Once you reach acceptance, you are aware that your child is different, but these differences no longer matter to you in the way that they once did.  You no longer seek to change your child with the intent of making them seem “less different”.  This doesn’t mean that you don’t help your child overcome the limiting parts of his or her disability.  It’s just that normalcy is no longer the goal.   You want your child to live a happy and fulfilled life, but you realize that the very definition of happiness and fulfillment can look very different than you once imagined. 

When you reach this stage of acceptance, you realize that your entire view of success, happiness, and possibility have completely shifted from what you once knew and understood.  You now see a much more expansive realm of possibility.  And then one day you wake up and realize that it is you who has changed as much (if not more) than your child.   That’s the moment when you know, that no matter how hard things get, it really and truly will be okay in the end.  

Welcome to the Sensory Blog Hop — a monthly gathering of posts from sensory bloggers hosted by The Sensory Spectrum and The Jenny Evolution. Click on the links below to read stories from other bloggers about what it’s like to have Sensory Processing Disorder and to raise a sensory kiddo!

1 comment:

  1. Oh - BEAUTIFUL.
    I think this may be my favorite ever of your posts (and, oddly, we wrote about somewhat similar stuff this month?!).
    There have been times when I too was in both positions - on the one hand where you are trying to do everything - all the treatments, all the worrying, advocacy, etc - and on the other where there's more acceptance of things as they are. Every once in awhile we get to feel in balance...
    Thanks and love,
    Full Spectrum Mama


Please add a comment here.