In my twenty-seven years I feel like I have overcome quite a
bit. I was diagnosed with a learning disability when I was twelve. I was
diagnosed as meeting the clinical definition of depression when I was fifteen.
Over the years this has been expanded to include an anxiety disorder and a
‘chemical imbalance’. At seventeen I was diagnosed with osteoarthritis in my
right knee – more commonly occurring in individuals three or four times my age.
However, none of those experiences prepared me for a meeting I was to have
regarding my daughter on an otherwise uneventful Thursday morning.
I sat in this small room with two doctors as they went
through their various assessments of her behaviour and why they felt her worthy
of the official diagnosis of “Autism Spectrum Disorder (ASD) – high
functioning”; also known as, Asperger Syndrome. As a parent, there was nothing
that could have prepared me for sitting in this room while doctors told me that
my perfect little girl may not be perfect. My heart sank, and frankly, I just
had an overwhelming sense of fear. That is a word that has taken many aback,
but let me explain.
When I heard those words about my child for the first time
all I could see was those people that would treat her differently because they
couldn’t see past that word: “AUTISM”. Would she ever be able to fall in love?
Would she get married? Would she have children?
These are all things I want for her. It breaks my heart to
think these life landmarks may be more difficult for her to come by.
After nearly two month to consider her future and talk to
others; most importantly my wife, with children or family somewhere on the
spectrum I have come to some realizations. The first and most important being
that she is still the same girl she always has been. She is a lovable, playful,
outgoing child who just wants to dance and sing. She is also going to be helped
by this official diagnosis. The Toronto District School Board will now be
legally obligated to meet her additional needs, where they were initially
sitting on their hands during her first year. And, of course, that is just the
beginning.
Meeting my daughter’s needs will be a much more involved
process than meeting my own was. My learning disability required a little bit
extra time on tests and gave me the opportunity of a credited study hall. Both
my wife (who is luckily acting as my rock during this trying time) and I will
be advocating for our daughter in some capacity for our entire lives. But
frankly; there is no other person in this world I would rather advocate for.
For other parents in a similar situation reading this,
please share your stories with me at glassjx@gmail.com.
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