Salty, Sweet and Just Right

This post goes out to Becky at Blessings Thru Raindrops. Her post about putting good stuff into the world that is filled with, well, put nicely, not a lot of good stuff, sounded like something I wanted to do too.

So here it is…

Charlotte’s response to the theme “A gift salty, sweet, just right.”

I grew up in Fort Lauderdale, Florida in a beautiful neighborhood called the Las Olas Isles. Our house was less than a mile from A1A and the Atlantic Ocean. It was a wonderful place to live and even as a child I was aware of just how special it was.

Sunshine.

Warm weather.

And a boat at my backyard dock.

I mean really, what’s not to love? Continue reading

The Outing Of Aspergers

As I look at this photo taken 21 years ago, I not only see a young me, and an even younger Ted, I wonder what was on my mind as I stood smiling at my camera wielding husband and holding our infant son.

Looking back at that wrinkle free face, I imagine I was enraptured by the newness of everything in my life. Married just two years, living in our first house, 1,300 miles from where I grew up and just eight, very sleep deprived weeks into my role of a lifetime.

And I imagine also it was the beauty of the falling leaves that got me to coax Neal into this photo shoot. Autumn was still so unique to me back then, having grown up in South Florida where the only thing I saw fall from trees were coconuts.

What also entered my mind as I gazed at this photo was how several autumns after it was taken life found us in a very different place, a place I could never have imagined that October day in 1991. In addition to two moves, my husband’s Ph.D. and a brand-new little sister for Teddy, in the autumn of 1995 we welcomed into our expanding family an unplanned addition named Aspergers Syndrome. Continue reading

Seven Years Later A Hurt Can Still Draw Blood

There is nothing to writing. All you do is sit down at the typewriter and bleed. Ernest Hemingway

Above: Hemingway’s writing studio in Key West, FL. Christmas morning, 2005

The first presidential debate was this week and it reminded me of what I dislike about politics, and more specifically, human interaction.

What’s coming is a hard sentence for me to write, it’s creating tension in me, speaking my thoughts, especially when they aren’t overwhelming positive. But since the purpose of writing is to explore our feelings, our humanity, here it goes…

I think we are all hypocrites.

I know I am.

And I wonder if we accepted we are all hypocrites would we get on better? Continue reading

Weekly Photo Challenge: Mine

Long gone is his red shirt with the stitches that spelled “Pooh”.

Instead he wears a thin coat of loved off fur.

His right ear had to be thoroughly cleaned during our first, and only, deep-sea fishing trip. I was five and the seas were high. It didn’t go well for either Pooh or I.

On his left leg are the results of surgery done by my eight year old hands.

When I was 12 he went on our round-trip Ft. Lauderdale, Florida to San Francisco, California family vacation. I left him in a hotel in Jackson Hole, Wyoming and we were 40 miles down the road before his absence was discovered. My sweet parents, without complaint, turned around and drove back where we found Poor held hostage by the hotel’s maid. She was going to bring him home for her child. Dad paid her ransom to get him back.

He has gone to college, survived my kids, and now rests in my bedroom’s window seat.

We have been together since I was five months old, given to me my first Christmas, 1965. It isn’t my wish to be buried, but if I were to be, my faithful Pooh would lie beside me.

When I think of what is mine – I think of my Winnie the Pooh.

Interested in being part of Weekly Photo Challenge? Click here.

The Circle Of Autism, The Circle Of Life

It has been a while since my last installment of Educating Teddy. It is my plan, or at least my hope, that upon the conclusion of retelling the story of my son’s childhood I will then begin the story of where Ted is now.

At first I thought it was for you, the reader, that I told the backstory. I thought I could share with you the lessons learned during his educational experience, and then examine the impact of his early years on where he is today.

But I have come to realize it is with selfish motivations that I take this approach, for it is me who has been helped in a way I had not foreseen. By reflecting on and writing our story, I have done the learning, and you, dear reader, have become not so much the recipient of my lessons, but a companion on this journey of discovery.

By opening up parts of me that have been sealed off for almost two decades, I break the isolation I once knew and embrace the community I now know.

Joining the blogging community is like being lifted off a deserted island and being placed into civilization.

And when I think of the isolation I have been released from, I think of a woman I had lunch with in 2005. My daughter Meg’s then art teacher was friends with Helen, a mother of an autistic son, and she wanted us to meet. Helen was 81 and her son Henry was 56. Helen had spent her entire mothering life in isolation.

For several hours I sat with and listened to this delightful woman tell me stories of what it was like raising a child with autism in the 1950′s. She did not have the option of sending Henry to school. Rather, her option, if you would even call it that, was to institutionalize him.

So she kept Henry at home and educated him herself. And he was still at home. Her husband had passed away almost a decade earlier and it was Henry and her.

There was no regret, no bitterness when she spoke and when the conversation turned from her son to mine she had only what I would call a voice marked with the flavor of curiosity. A natural curiosity about the opportunities being born four decades after Henry brought Ted.

“What has school been like for Ted?”

“What does he like to study?”

“What kind of work does he want to do?”

“Will he live independently?”

These were some of the questions she asked.

These were the questions she never got to ask for Henry.

I don’t know why life happens as it does. Why Henry, born in 1949 and severely challenged by autism had so few opportunities. Was it being born deep in Dixie during a time when prejudice dominated? If our community was reluctant to educate its black citizens I cannot imagine they embraced those with disabilities.

What I do know is the American with Disabilities Act and IDEA came too late to educate Henry, but it was there for Ted, and maybe for your child. And even when times were difficult for us, when we were stonewalled and told “we don’t do that” I knew we had a law to back us up. So when I finally found my voice, when I was finally strong enough to adamantly push back, I knew I could.

I knew my voice had to be heard as Helen’s never could.

When the day comes I can write to you, my community, about Ted making it out of our home and into his own, I will do so with Helen and Henry on my mind. For it is my desire to seek and celebrate independence not just for our child, but for everyone.

I end with a quote from Ted, written in his self-titled Freedom Manifesto…

Those who would defend their own freedom but fail to stand up for that of others fail to see that only in a society where all individual freedom is valued above all else are they free at all.