Posts Filed Under SPD

Letters to Kindergarten: Who are You?

November 13, 2012 by in Anxiety, Avoiders, School, SPD with 3 Comments

When I let myself think about starting kindergarten, I am terrified. It overwhelms me to think of all the hurdles he will encounter. If it were any other child, one of my students instead of my own son, I would have a list of solutions to possible problems already. But, lately, I just can’t get past the fear.

In a effort to make this logical rather than emotional, I decided try a strategy that I use when making goals and plans for my students…think about things from their perspective. What are they thinking? How would they react and why?

So, I started thinking about what would say, if he had the chance, to kindergarten. And, this series was born. This is the first of many letters I will write to kindergarten, from O’s perspective. To ask questions. To discover solutions. …continue reading

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Thinking differently

November 12, 2012 by in Autism, School, SPD with 3 Comments

November 6, 2012…later in the day…Why it matters part II…

As soon as I picked Ewan and his brother, Vaughn, up from school today, they honed in on my ‘I voted’ sticker, and excitedly asked, “Did you vote today mom?”

I replied, “Of course, I voted!  It’s my duty.”  The historian in me giggled with delight as I explained all about voting to the boys.

Ewan seemed very excited about this, and asked, “So, can kids vote?  I want to vote.”

I shook my head, “No, kids can’t vote.  You have to be 18 years of age to vote.”

Ewan frowned, “Why?  That’s not fair!”

I patted his shoulder quickly before he squirmed away, and said, “Well, voting is a serious responsibility and you have to be able to handle that responsibility before you vote.  And that means you have to be a little older.”  When Ewan continued to frown at me and mumble something about unfairness in the American political landscape, I said, “You know, I wanted to talk to you about rights today anyway.  So even though you don’t have the right to vote just yet, you do have another right.”

Excited, he asked, “What right?”

I smiled, thinking maybe I’d found a segway into my next topic, “Well, it’s called the right of inclusion.”

He groaned, “Inclusion?  That’s not fun.”

I laughed, “Well, maybe, maybe not, but it’s still a right.  And it’s something you should know more about.” …continue reading


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Living in “Interesting” Times

November 11, 2012 in Autism, Behavior, Marriage, Parenting, SPD with 7 Comments

My husband is a Naval Officer. We’ve been married for 17 years and have three children together. Our two boys, ages 5 and 4, are on the autism spectrum. As such, they have a boat

The Elf on the Shelf

November 10, 2012 in Autism, Holiday, SPD with 4 Comments

This time last year, I was contemplating “adopting” an Elf.  You know, an “Elf on the Shelf”. Basically, you “adopt” an Elf, name it (because naming the elf gives him his magic), and place it in

Numb: A Follow Up

November 9, 2012 in Autism, Parenting, Psychologist, SPD with 4 Comments

I lasted posted about feeling numb the day my son received his diagnosis. When I wrote that, it was the morning following his diagnosis and I was at work. My son was sleeping when I

Things Not to Say to a Parent of a Child with Special Needs

November 8, 2012 in Autism, Humor, Language, Parenting, Social, SPD with 10 Comments

I know most people mean well. People do not know what to say, or they feel compelled to try and make you feel better. Some are genuinely trying to be positive and others, well they

One Pool, Two Pool, Old Pool, New Pool

November 6, 2012 in Autism, Avoiders, SPD, Therapy with 4 Comments

When my son was diagnosed, I never suspected that my child still had motor delays.  Sure, he did everything late; he rolled over at 8 months, crawled at 11 months, walked at 16 months, and

Desperately Seeking Suggestions

November 5, 2012 in Advice, Anxiety, SPD with 7 Comments

I am new to blogging. The series of pieces I wrote on here are my first and only experience dipping my toe in the blogging pool. I know we share our experiences and offer support,

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