January 30, 2014
Note: I asked Howie if I could share this story (and parts two and three) here. I told him that I had a blog and that I liked to write about things that happen in our lives on it. His response? “Sure. You can share this with the blogosphere.” Well, okay then.
Second note: While this is part one, the story actually comes after parts two and three chronologically. But I felt like I had to share this one first. I hope it makes sense in the long run.
I was finishing up at work tonight while Howie was playing on the iPad. He was with me tonight as he is most nights that I’m at the sensory gym.
I closed up the computer and it made that whirring noise that laptops make as they wind down to hibernate.
“What’s that noise?” Howie asked. “The one that sounds like…” and he mimicked the noise perfectly.
“Ah,” I said. “That’s the computer shutting down. You made that sound exactly right.”
I paused for a moment.
“You’ve always been good at that,” I told him. “It’s all part of that amazing brain of yours.”
“It’s in my soul.” he said.
“What? What do you mean?”
“My gift. It’s in my soul. It will always be a part of me.”
I stared at him from across the room. He never looked up from his iPad the whole time. But his words moved me to my core.
This incredible child of mine. He knows what he has is special. Different not less.
“You’ve had that gift since you were born you know,” I said. “Like that song ‘Born This Way.”
He gave a little chuckle. “Oh yeah. It is like the song.”
And while maneuvering around his Minecraft world he quietly sang “You’re on the right track baby you were born this way.”
I walked over to him and gently kissed him on the cheek.
“I love you sweetie. And that amazing brain of yours.”
“Wanna see my minecart move on the tracks?”
Yes. Yes I do.
“There’s nothin’ wrong with lovin’ who you are
She said, ’cause He made you perfect, babe
So hold your head up,
girl and you’ll go far
Listen to me when I say
I’m beautiful in my way
‘Cause God makes no mistakes
I’m on the right track, baby
I was born this way” – Born This Way by Lady Gaga
Parts Two and Three (which are really parts one and two) about how Howie learned about autism are coming soon…
January 28, 2014
A few weeks ago, we got our notice for our annual IEP meeting for Howie.
And just like every other notice we’ve received for the past five years, this one included a one page purple sheet addressed to us as parents:
Please take a few moments to respond to the following questions. Please return this completed sheet in the enclosed envelope. Your comments will help the whole team develop an appropriate education program for your child.
1. What concerns do you, the parent (and student fourteen years of age or older) want to see addressed in the student’s educational program?
2. What are the student’s educational strengths, areas of interest, significant personal attributes, and personal accomplishments?
3. What is your vision for your child? What would you like your child to be able to do within the next 1-3 years? Beginning at age 14, think about your child’s preferences and interest. Also think about desired outcomes in adult living, post secondary and working environments.
I’ve always taken these very seriously. I return them every year with long detailed responses to each question, usually going on to the backside of the paper. I felt like if they were asking, I was going to answer.
I sat with the sheet in front of me for a while. I thought about how this whole year we’ve been working with Howie to help him identify his sensory needs and coping skills to help him stay in the classroom when he can, but also know when he can’t be there. And to know that that’s okay. We’ve talked about him being his best advocate and using his words to explain what he’s thinking and feeling in the moment. And working with his team to respect that and to really listen to what he’s saying.
For the first question…well I decided the best person to ask was Howie himself. Waiting until he was fourteen didn’t make any sense. So I asked him to tell me what was hard for him. We talked about the times when he gets stressed and what calms him down. I translated it into five issues we’d like addressed in this year’s program:
1) anxiety and stress in academics addressed through accommodations (specifically during time tests, reading out loud to peers, patience with learning new topics)
2) access to new sensory tools and accommodations for individual/group work (scribe, extended time, ability to type answers)
3) work on social/emotional regulation within the classroom space
4) development of self-advocacy skills
5) implementation of programs to work on rules/consequences and taking responsibility for his action.
My answer to the second question remained pretty consistent from the past five years. I wrote that he’s very bright – strong in science and math concepts and loves social studies and history. He loves to read on his own terms and enjoys project time and projects with some structure but without too many constraints. He likes to feel like he’s the teacher and loves feeling popular in his class.
It was the vision question that made me stop for a very long time.
My vision statement for the past four years was this: We want Howie to show what he could do academically without his behaviors getting in the way.
I read that now and I cringe. I don’t even want to write that here. But truth is that in the beginning I didn’t know what I know now. I desperately wanted his teachers and the staff to see the bright incredible boy that I saw. My concerns – my fears – were that they would never see that he had this incredible brain, a wicked sense of humor, and they would never know that he could read and write and draw just like every other kid in the class. I thought that his “behaviors” would keep him out of the classroom and away from the things that he excelled at.
I didn’t know what the behaviors meant. That they weren’t something to extinguish. That we couldn’t “compliance training” them away.
Now I know.
I know that behavior is communication. I know that stimming is not only okay, but necessary. I know the importance of learning how sensory and calming strategies work in different situations. I know to look at my kid as my kid – not a series of antecedents, triggers, and behavior plans. I know now to respect what he’s doing and listen to what he’s saying because by doing that – that’s how he achieves success. Academically, socially and emotionally.
He has that success now with his current teacher and aides. Educators who look at him as an individual and work with his strengths to overcome his challenges.
It was time to put all that into writing.
What is my vision for my child?
We would like Howie to be happy and enjoy school and learning in a classroom environment that meets and supports his needs. This means helping him become a better self-advocate while creating a program that fits his individual strengths and challenges, with accommodations and supports necessary for academic, social and emotional success.
On Monday, we will sit down with his whole team and write an IEP that does just this. As we write objectives for pragmatics, sensorimotor breaks, and social/emotional growth, the major thread through it all will be to help him find ways to feel good and comfortable in his own skin, to feel respected for his differences, to advocate for himself and to – plain and simple – be happy.
That’s how he’ll show them what he can do.
By being himself.
“See my reflection change
Nothing ever stays the same
But you know the names The Game
We don’t know what it means
Nothing’s ever what it seems
I see the line in the sand
Time to find out, who I am
Looking back to see where I stand
Evolution, Evolution” – Evolution by Motorhead
January 14, 2014
I went into our local Paper Store to pick up a gift for a friend.
And it was like the universe was trying to tell me something after my last post:
It will be going up on the wall in Howie’s bedroom. As a reminder for us both.
“I love you You love me
We’re a happy family
With a great big hug and a kiss from me to you.
Won’t you say you love me too” – I Love You from Barney
January 10, 2014
This is a hard one to write.
A few days ago, my friend Jess met me at the sensory gym with her daughter Brooke. It was the last day of our very long holiday break. The exact purpose for the gym unfolded before our eyes as Howie and Brooke played together in the gym space while Jess and I talked.
After about 20 minutes of playing and running around, Howie came over to me and climbed into my lap. Jess took out her phone and snapped a few photos. She sent them to me later that afternoon:
(photo credit: Jess)
I spent the rest of that night thinking about those photos.
True confession time?
When I saw that last picture, my stomach hurt. My heart hurt.
I could only see the sensory seeking in this picture.
His hand in my hair. Crawling all over me.
The constant requests for squishes. Asking to “tunnel” : when he puts his hands on my neck and asks me to press down on his hands with the side of my head. Begging for “snuggles” that aren’t really hugs. The “mom will sit on my feet” demands.
I saw a dysregulated kid who had been out of school and out of a routine for too long.
I sent Tim this text with the last photo: “Jess captured how I spent all of vacation.”
“Yup.” was the reply back.
The following morning, I changed my personal Facebook profile picture to that last photo.
The comments I got from friends and family ranged from “Love is…” to “That is just precious!” to “So sweet!”
And the one that made me cry: “That’s true love. You being a non-hugger and all – this is ALL love. Beautiful!”
Guilt came flooding in.
Everyone else saw love. Affection. Connection.
The emotions I didn’t see.
I get so wrapped up in everything SPD/autism and looking for the meaning and cause of every single action and reaction…
I sometimes miss the beauty and the “normalcy” of these moments.
Of so. many. moments.
Taking him out to shovel the snow is “heavy work”, not just an outside fun activity together.
Swinging high on the swings has a purpose, not play.
A hug isn’t a hug. It’s a need for deep pressure.
Truth is, I’m the only one he will hug and snuggle with like this. He refuses all personal touch from his dad and older brother and relatives. He will squish under blankets and pillows, but skin to skin touch is reserved for me. Has been since he was born.
Because I know too much, I saw it as a sensory issue for him.
But to everyone else, it’s a loving bond between mother and son.
After reading those comments, I clicked on the photo on my phone and looked at it again.
I took a step out of my “autism mom” role and became “Mom”.
because I needed to look at it again…
In those photos there is the smile. The calm. The love.
I can see that’s what Howie sees when he looks at me.
This is our connection. Our affection.
His safe place. Where he feels the most at peace.
I see it all.
And I feel at peace now too.
“love I get so lost, sometimes
days pass and this emptiness fills my heart
when I want to run away
I drive off in my car
but whichever way I go
I come back to the place you are
all my instincts, they return
and the grand facade, so soon will burn
without a noise, without my pride
I reach out from the inside
in your eyes
the light the heat
in your eyes
I am complete
in your eyes” – In Your Eyes by Peter Gabriel