Tuesday, October 22, 2013

The burden


The words slipped out of his mouth with seeming ease. They were spoken before I could stop them. “Of course, you love your son, but I can’t imagine the burden of living with him.”

He was attempting empathy. He was trying to understand my life. But he had it all wrong. Though I was surprised by his words, I didn’t respond. Perhaps because of my silence, he thought I hadn’t heard. He said again “I can’t imagine the burden you carry. All the work.”

He couldn’t imagine my life. I understood that. Fair enough. Perhaps I wouldn't understand his life either. It can be hard to understand a life you haven’t lived.

I watched him shake his head again saying once again, “all the work, the burden of it all” and then trailing off. In total he used the word “burden” four times, making it clear he saw the only sadness in my son’s existence. I smiled politely, responding, “I don’t see Sam that way.”

I thought about his words after he left. About how someone, without ever meeting Sam, could sum up his life into the single word: burden.

If I thought he would have understood, I might have partly agreed. Sam IS a lot of work. He had that right. I would have then suggested most everything worth doing requires effort. Most of life’s achievements, large or small require work.

I might have pointed out the difference between the words “work” and “burden.” I might have said I look at our life with a sense of satisfaction. That we are in a good place, that there is joy in our life, joy in our home.

I don’t think he would have understood.

There was a time when his viewpoint might have crushed me; when I would have felt compelled to argue Sam’s worth. A different viewpoint no longer defines us.

A single word does not define Sam.


Follow us on Facebook at https://www.facebook.com/BlendingWithAutism



Friday, October 11, 2013

Our lens



In the beginning I had a plan. I had certain dreams. Certain expectations. But life doesn’t always respect a plan. That is how it was with us. There was the “plan” and what actually came to pass.

Our early years became a blur when Sam showed signs of atypical development. I was hurled into survival mode while trying to make sense of it all. At the insistence of the specialists and the folks at Early Intervention, survival quickly morphed into “fix it” mode, effectively entering us into a war with destiny. Everyone was consumed with changing the path we’d been put on. They told me time was my enemy. I struggled to help Sam keep up as time spun relentlessly.

Each day was a roller coaster of highs and lows; a jumble of emotions, intricately tangled together, exceeding what seemed humanly possible. Emotions so big I thought they’d swallow us whole. I struggled; enamored with the child I had and saddened by everyone’s desire to change him. Unsure of what to do.

Sam, all the while, took most days in stride; forcing us to slow down, even stop to find joy in little things we might have otherwise missed. Within the sea of doctors and experts advising us of how to “fix” our child, Sam was the “voice” of reason, compelling us to find balance between the world we were told we wanted and the world we’d been handed. 

In a blink, eighteen years passed. And in spite of everyone’s best efforts, Sam’s path never changed. The only path that changed was mine.  

Raising Sam changed forever the lens I used to view life. He altered every perception, every understanding of what was important. He challenged every belief I held dear. He humbled me. He made it impossible to ever be the careless person I once was.

At first it was hard to let go society’s image of perfection. I didn’t know anything about raising a child with a disability. I was flying blind. Some days seemed endless. Progress was often slow. But somehow on the most difficult days I’d look into a pair of bright dark eyes and see a smile with the power to melt every frustration, to make everything inexplicably right. I knew the warmth of a hand that reached into my heart, compelling me to surrender.

Slowly over time I reconciled myself to the challenges; learned to see the perfection in what we had. And eventually there was peace. As we charted our own course I finally opened my eyes and saw before me the child I never expected, but knew beyond any doubt was exactly the child I’d waited my lifetime to find.

And it was good. 


Follow us on Facebook at https://www.facebook.com/BlendingWithAutism



Thursday, October 10, 2013

Seizures and dog biscuits


Sam had a seizure Sunday. He stood at the top of a flight of stairs and stumbled as the seizure began. Fortunately our quick-witted puppy, Mr. Dog, saw him standing precariously and sounded an alert with a loud bark. I was by Sam’s side within a second.

I held Sam safe until the seizure stopped and then carefully sat him down on the stairs, holding him until I was certain he was OK. Certain that he was stable. Mr. Dog stood at attention behind Sam, waiting I am guessing, for the very same assurance.

As the seizure waned, Sam looked at me blankly, unsure of what was going on. He announced his tongue hurt, shook off his confusion and went about the remainder of his day, seemingly unscathed. Crisis averted, Mr. Dog wandered off to resume his nap. Everyone was fine it seemed. Except me.

I couldn’t wipe the “what might have happened” image from my mind. I needed something to refocus. With that in mind, I called Sam to make dog biscuits for Mr. Dog as a reward him for watching Sam so carefully. I hoped the busy work would be distracting. Still, I couldn’t turn my mind off. I kept envisioning what might have happened.

As we worked, I looked over at Sam. He was by my side mixing ingredients, helping me roll the dough then methodically cutting the biscuits into bone shapes. He sang happily as he placed them neatly on the pan. I admired his serenity as he approached the task at hand.

That is how it is with Sam. He lives mostly in the immediate. What is past is past. The future is the future. His places his attention squarely on what surrounds him. He compelled me to join him in the present; drawing my attention to a happy moment I would have otherwise missed. He provided the grace note to get me through the difficult thoughts.

I looked around again. Calm permeated the room. Sam was safe. A phone call to the doctor would be made on Monday morning. The biscuits were in the oven. Mr. Dog was sniffing something good in the air. We were lucky today. Lucky indeed.     


Follow us on Facebook at https://www.facebook.com/BlendingWithAutism



Friday, October 4, 2013

Patience


Patience.
We start.
Methodical.
Consistent.
Patient.
Seemingly standing still.
Present the information.
Over and over.
Again and again.
Ask the question again.
And again.
Try, try again.
Not quite.
Why didn’t he understand?
He wasn’t ready.
Another day it will happen.
Maybe tomorrow.
Try again.
Today was the day.
He understood today.
It just finally clicked.
Why today?
He was ready.
He was finally just ready.
All the pieces came together.
The pieces fit like a puzzle
It clicked.
It snapped into place.
He got it.
Victory at last.
A small cheer.
We move forward.
We move on.
Another concept.
More to learn.
We begin again.
Patience. 


Follow us on Facebook at https://www.facebook.com/BlendingWithAutism