What’s so special about MSD?

Photo-0043I often mention MSD, either in person or online. It’s MSD this, MSD that. When the old school building was torn down because a new school building had opened, I expressed sadness about the loss of the old school building. When a friend from MSD lost her son in early June, I fell to pieces over it. Jimmy Glover died at the end of July, and though I hadn’t talked to him in twenty years, I felt moved to post something about him on Facebook. Most recently, I stated that I want to see my friends from MSD before the year is over.

MSD–or Michigan School for the Deaf, if you got enough wind in your lungs to say the whole thing every time–is the primary school for the deaf in Michigan. There are other schools where the deaf are taught, but from what I gather, they are regular public schools where the majority of students are hearing.

I’m trying to write something meaningful here, something that will properly convey why MSD is special, but I fear I’m not a good enough writer to do MSD the justice it deserves. But I’ll give it my best shot.

Every former MSDer I know still looks on MSD with fondness. The place was more than just a school for most of us. It was a home. We lived five days a week there and went home for the weekends.  Some of the students had attended the school, living in the dorm, since they started kindergarten. Others joined the school in later elementary grades, or junior high and high school. Many were transferred from Dearborn and Detroit schools where there were programs for deaf and hard of hearing students.

But wherever they came from and whenever they enrolled at MSD, most of them already knew each other. They had attended camps for the deaf and other deaf events since early childhood. American Sign Language was their first language. Most of them could talk using their voices if they had to, but many preferred not to. Some were completely deaf. Some were deaf, but did have a little bit of hearing. And some were hard of hearing, like me. But whatever category you put them in, MSD was like a comfort zone for them, a place for them to be with others who were like them.

At MSD, no one had to explain that they couldn’t hear you. Everyone got it. So, that was one frustration we didn’t have to deal with. Several teachers and staff were also deaf, and those who weren’t deaf were understanding of the students’ needs.

I don’t want to turn this into a rant about my experiences at the Lapeer public schools I’d attended, so I’m going to try to be brief about it. I mean, it wasn’t always bad. There were some good times. There were students who I got along with and there were teachers who were patient and understanding. But on the flip side, there were many very stressful and humiliating situations.

It wasn’t so bad in elementary school, but it really took a nosedive in junior high and it only got worse when I started high school. I wouldn’t say it was all because I couldn’t hear very well. My twin brother is also hard of hearing and he did all right in the public schools. But me, I was depressed all the time. I was terrified in school. When I got home after school, I’d go straight up to my room and spend the whole day watching TV or reading. I did not have a social life.

My freshman year ended. I had my summer vacation and shortly before school started back up, the depression and fear returned. I did not want to go back. I think it was my mom who suggested I enroll in MSD instead. But wherever the idea came from, once it was in my head, I was all for it.

I had been to MSD several times before, to see Betty Brown, have my hearing tested and get new hearing aids set up, but I had never thought I’d actually be a student there before my sophomore year. But once the idea was in my head, I was hellbent on making it happen. I felt that MSD was the change I needed.

It took some time, though. We had to go through a few different meetings with the Lapeer Board of Education. School had already started, but I wasn’t attending yet. Some of the people at the meetings did not think MSD was the right place for me. But finally, about a month after school had already started, I was cleared to go.

I didn’t know sign language when I first started at MSD, but there was Tina Takacs, Margaret Barker and sometimes Marilyn Belsky who put in the effort to teach me, and there were students who showed me signs. I learned sign language and improved, but I was always pretty much in the beginner’s stage.

I’d be lying if I said MSD was a hundred-percent positive experience for me. Sure, there were plenty of negative experiences. I was still a shy, awkward guy who didn’t talk much. I still had nervous issues and I’d get depressed at times, and I didn’t quite know how to fit in. I still had many of the same issues I’d had at the Lapeer public schools. However, at MSD, there were far more positive experiences than negative experiences. I was actually happy there and living in the dorm allowed me to have a social life.

As I learned more about deaf culture, I began to see myself in a more positive light. I learned that being deaf or hard of hearing does not mean one is impaired. I learned that deaf people do not see themselves that way and I wanted to think the way they do.

Going to MSD is one of the best things I’ve ever done. It really turned my life around. I’m still in touch with friends from there. I wish I could see them in person on a regular basis, but they all live in different parts of the state and it’s hard for me to get around and see them. But we keep in touch on Facebook.

For Joshua’s Mom

One of my best friends had the funeral for her son today. I’ve had it on my mind all day. I love you, Brooke. I know it’s going to be hard for you and your family, but I hope everything works out somehow.

And I wrote this song:

The moment I heard the news,
My heart broke and tears flowed.
I couldn’t understand how this happened.
Something isn’t right in the world.

I asked God, “What is it with you?”
“Why would you do this?”

I guess He has His reasons.
He’s always got some plan.
Though it makes no sense to us,
We’ll all figure it out some day.

I know it feels unfair.
I remember how excited you were
And we were all suggesting names.
Then came the day your son was born.

There was no doubt that he was special
Everyone could see that he had spirit.
The way he was always smiling,
We knew he was happy and loved.

I wish there was more I could do.
I know you have a hard road ahead.
There’s a lot to tunnel through,
But light can be found at the end.

Zero-turn Mowing and Ribeye Steak

My dad talked me into mowing his lawn today, with his zero-turn lawnmower, which I have never operated before. Zero-turn lawnmowers do not have steering wheels. Instead there are two bars in front of you. You push the left bar to turn right and you push the right bar to turn left. Heh! How does anyone keep an arrangement like that straight? On top of that, they are freaking fast lawnmowers. I almost ran into a tree and the natural gas tank, and I quickly decided I wasn’t going to mow within fifteen feet of the pond.

Afterward, we went to Apollo Family Restaurant (Davison, MI) where we both had ribeye steak.

Yesterday

The White Sox beat the hell out of the Tigers yesterday and then the Red Wings got their asses kicked. But it was a good day. Spent the day at Mom and Dad’s. My brother brought over his girlfriend and we spent a lot of time up in the bar singing karaoke. For the first time, I actually worked up the nerve to sing karaoke. I sang Bon Jovi’s Blaze of Glory and Breaking Benjamin’s Blow Me Away. Well, sort of. I know both songs very well, but a lot of lines slipped my mind while trying to sing yesterday. I probably sounded like I had a dried up frog in my mouth too. But it was fun.

Disturbance

Normally I don’t complain when Jehovah’s Witnesses turn up at my door, but this morning I really wasn’t in the mood to be disturbed. When Luci started barking, my first response was to tell her to be quiet. But when she wouldn’t stop, I got up to see what the deal was. “Oh, God,” I said when I saw the white SUV and two women dressed generations out-of-date. Of course I opened the door and said “Thanks.” when I was handed the little brochure, but as soon as I closed the door I tore that brochure up and dropped it in the garbage.

Thank you very much for breaking my concentration, ladies. And no, I’m not going to join your Kingdom Hall.

But they are not the reason I didn’t get 2,000 words today.

2015 Is Here

We’re here. This is the year Marty McFly went to in Back to the Future Part II. We still don’t have flying automobiles, hoverboards, automatic dog walkers, “Power laces, all right!” shoes, or those really cool Pepsi cans. But we do have a lot of neat stuff, so science fiction is happening in some ways.

Looking back on 2014…. Well, to be honest, I don’t really want to look back. I want to look forward. Now that we’re here, I want to look at 2015. I want things to happen in 2015, things that I can look forward to. Sure, I’ll still reflect on things from the past, whether good or bad, but right now I’m not in the mood.

But I will say this about 2014, it was a decent year, with the usual ups and downs, some of it heartbreaking and some of it not bad at all. I did manage to make another short story sale. It’s been quite a while since I last made a sale and it’s good to be back in the game. I also finished that novel I had been working on for too long and I’m already 20,000 words and 98 pages into my next novel. So, I would say 2014 was a year I accomplished a few things.

I plan to step up my game in 2015. I want this to be a more productive year than last year was. I also hope to make a few more short story sales and land an agent for my novels. I want this to be a good year.

2015, we made it.

My World

On Facebook, a friend shared this link: I’m Deaf and I’m Totally Cool With It, Thanks.

What I meant to be a short comment turned into the lengthy article below.

———-

I’m hard-of-hearing, quite far from being deaf as I can hear pretty much everything, a floorboard squeaking, the hum of the furnace, birds outside my window, though I don’t think I hear it all as clearly as a person with good hearing would. If someone speaks to me, I will hear their voice, but I can’t make out what they said about eighty percent of the time, unless they’re willing to repeat themselves, often three or four times before I understand them.

I don’t wear hearing aids. I’ve never been able to adjust to hearing aids. All hearing aids have ever done for me is amplify sounds to the point that they are annoying, and any speech I heard was vastly distorted and even harder to understand. A few years ago, I decided to give hearing aids another try. I had hoped that the newer technology would make a difference. But it didn’t. People told me I just needed to get used to them, but I gave them a chance. I wore the hearing aids every day for a couple of months, and then I was putting them in less and less. I don’t want to be trying to get used to hearing aids for months. I had to keep taking them out just so I could understand what people were saying.

It wasn’t so long ago when I thought I would go for cochlear implants. But then I changed my mind. First, because (as I understand it) the process of having cochlear implants put in would involve cutting the nerves that go from my brain to my ears.  My ears would become useless things sticking out from the sides of my head. I would never again receive sounds through my ears. All hearing would completely depend on a mechanical device that would be inserted in my head. I also began to suspect that cochlear implants really aren’t that much different from hearing aids, that like hearing aids they amplify sounds and distort speech. Some people might be able to get used to that, but I never could.  I’d go crazy if I had to be stuck in that world for the rest of my life. If I decide to turn the cochlear implants off, I would be stone deaf.

Because I’m hard-of-hearing, I’m used to the world of sound. I’m comfortable here. I don’t want to lose the hearing I have. This is why I wear ear protection when shooting guns or running chainsaws. I don’t ever want to be where I can no longer hear the sounds I enjoy, but I understand why people who are deaf to the degree that they can hear almost nothing or nothing at all would prefer to stay that way. Most of those who are deaf that I know personally do have a degree of hearing, but I imagine that what they hear is very densely muffled, to the point that they barely acknowledge it. Sounds don’t matter to the deaf the way sounds matter to the hearing . That’s their world, they’re comfortable there. If the deaf were somehow made hearing, the world of sound would likely be strange to them and they might be unable to adjust to all the noise.

Sometimes I feel like I’m stuck in the middle, between the hearing world and the deaf world, and can’t really fit into either world.  I wish I could understand the hearing people in my life better. I think it’s just as frustrating for them as it is for me when we communicate in person. Some people think I can read lips, but no, I cannot. If I made out anything you said, it’s because I heard you.

I would also like to be able to hang out with my friends who are deaf without feeling like a burden for them. I’m way out of practice with ASL. I don’t know anyone in Lapeer who uses ASL, so I haven’t had anyone to sign with since my last year at MSD.  I got a video phone last year so a friend and I could sign with each other and get my skills up to where I can at least hold a conversation in ASL with another person. But we haven’t been able to use the VP that much and I still have a lot of work to do.

The Return of Anxiety

It was about a week ago when I had a total meltdown. I had been feeling great for quite a while, confident and secure. I wasn’t worrying about much. I was having fun, goofing off and enjoying myself. And then the meltdown happened. One minute I was fine, the next minute I was completely aware of how stupid and annoying I am. A wave of depression washed over me and I felt like I owed everyone an apology. An apology for what? I don’t know. I guess for existing within their range of awareness.

This happens once in a while. I usually choose to get drunk when it happens. Yes, yes, I drink, well, often. But usually I drink because I enjoy it and not as a means of comfort. When I’m in a total slump, I drink because it gives me some measure of peace. It numbs my senses to whatever is bothering me. By the time the alcohol wears off, the worst of whatever it was that had me so down will be behind me. At least that’s how it usually works out.

But even though the worst is behind me, there’s a sort of recovery stage that follows. I have to rebuild my confidence. It’s a slippery slope. I gain some ground and I lose some ground, and eventually I make to the top of the mountain again. Eventually I will be able to stop second guessing myself and everything will be dandy.

This anxiety, or whatever you call it, might well be over nothing. Right now, though, I’m not so sure that it is. But whether it’s over nothing or not, I’ll make it to the top of the mountain, eventually.

My Childhood Home

This is the house I lived in when I was kid, all done up in Sims 3. I lived there from the time I was a toddler until I was thirteen. It’s the setting of the Where I Want to Be song that I posted some weeks ago. Not everything measures up quite right, but it’s close enough. The outside siding had been yellow instead of white, but the Sims didn’t have a yellow siding that looked right. The furniture is placed as I remember it best, though I might be wrong about some thing.

house1

The front.

house2

The back. The deck and patio were not there in the beginning. I remember helping my dad build the deck. I’m guessing I was around five. The patio came soon after the deck, My brother, my sister and I had our handprints in the corner that is not touching the deck or the house.

house3

I chose brightly colored furniture just so it would show up better, but much of our furniture was dark colored. The walled-in spaces between the rooms were closets. And that door by the refrigerator, that was where the basement stairs were, but the Sims were being a pain in the ass about fitting the stairs in there, so I left them out.

house6

The basement. The wall in the middle wasn’t always there. My dad built that when I was about eight or nine so he could have a band room separated from the rest of the basement. The room behind the stairs, that was where the washer and dryer were. There was also an old junked up motorcycle leftover from my dad’s teen years, and an old coat hanging on the wall, dirty, dusty, and infested with spiders. The space behind the stairs was more or less a place to store junk.

 house4

We built the garage when I was around eight. I remember helping my dad with this too. The space between the garage and the house was a room where my mom had her hair salon. I wanted to include that room, but the Sims wouldn’t let me make a wall from a ground level building to a building on a foundation, so that’s another thing I was forced to leave out. So, my mom had a hair salon and my dad did a lot of auto body repairs in the garage.

house5

When I was around ten, we added onto the house. We moved the deck back, built a family room with a fireplace and a bar. We also built a larger bedroom for my parents. My brother moved into their old bedroom and I had a room to myself.

The house was on an acre of property. There was a hill in the backyard. The bottom of the hill was where we rode our motorcycles. The woods were behind the property. There were many other houses in the neighborhood like ours.

~

It’s been a long road.
So many days have gone by.
There are times I will always remember,
And I still have the old pictures.
I’m sitting here thinking
How I’d like to be there again.

When I was a kid we had a house
At the end of Big Buck Lane.
The world wasn’t much more
Than our neighborhood,
But that was all we needed.
In the spring and summertime
We’d ride our bikes where we wanted,
As long as we stayed within our limits.
It was just three short streets,
But I had felt free.

I want to be there again.

Sometimes we’d sit on the grass
By the basement window
And listen to mom and dad’s
Band practice after sunset.
And I remember playing basketball
On the patio beside the deck.
We had no hoop to shoot for,
But still we managed to score.
Life wasn’t always easy,
But I had felt at peace.

I want to be there again.

It was a time when I was pure at heart
And life was new and full of adventure.
The trails in the woods were haunted war paths
And the sandpit had buried treasure.

Our weapons were cap guns
And plastic bows and arrows.
Sometimes swords and knives
Were the juicer choice.
Before Nintendo came into our home
And motorcycles were what we rode,
Before we got into bigger things,
That’s where I want to be.

I want to be there again.

Where I Want to Be

It’s been a long road.
So many days have gone by.
There are times I will always remember,
And I still have the old pictures.
I’m sitting here thinking
How I’d like to be there again.

When I was a kid we had a house
At the end of Big Buck Lane.
The world wasn’t much more
Than our neighborhood,
But that was all we needed.
In the spring and summertime
We’d ride our bikes where we wanted,
As long as we stayed within our limits.
It was just three short streets,
But I had felt free.

I want to be there again.

Sometimes we’d sit on the grass
By the basement window
And listen to mom and dad’s
Band practice after sunset.
And I remember playing basketball
On the patio beside the deck.
We had no hoop to shoot for,
But still we managed to score.
Life wasn’t always easy,
But I had felt at peace.

I want to be there again.

It was a time when I was pure at heart
And life was new and full of adventure.
The trails in the woods were haunted war paths
And the sandpit had buried treasure.

Our weapons were cap guns
And plastic bows and arrows.
Sometimes swords and knives
Were the juicer choice.
Before Nintendo came into our home
And motorcycles were what we rode,
Before we got into bigger things,
That’s where I want to be.

I want to be there again.