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Karen Lynn Vidra, The Texas Tornado

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     Kody has an invisible disability that doesn't usually manifest itself; yet it's caused him to have no friends because of the stigma it carries. This is his story.

Image (C) 2009, Karla Dorman.

Kody Wilbright-Abramson is my name; I am sixteen years old and look like your average teenaged boy:  tall, rather stocky in build, with long ash-blonde hair that's longer in front than in back, blue-green eyes, a long Roman nose, and a thin-lipped mouth, as well as a chiseled face.  I am quite good looking as far as appearances go; then why in the hell don't I have any friends?

Oh, I know why.  It's because of my stupid disability.  I have what is known as an "invisible" disability:  you can't see it; yet it's there, stalking me like a lion, and most people don't even know I have a problem unless I decide to throw a seizure, which is how my disability manifests itself.

I have epilepsy.  When I was like six years old, I fell out of a tree while playing and landed on my head; ever since, I have seizures.  I take meds to control them, but once in a while, a seizure likes to sneak out and catch me off guard.  I have had 'em in school, at church, at home, even out in public; I usually end up doing it in front of people, and then they move away from me like I'm carrying the bubonic plague or something.

I have anywhere from two to six seizures a year, sometimes more, especially if I am stressing out about something.  Some people say I am a panic attack waiting to happen or call me a walking panic attack.  Maybe I do panic or worry too much; not good for the seizures, but at times, I can't help it, especially when it comes to mega tests at school or worrying about if I will ever land a girlfriend or get a job.

Most people don't want to hire me because "I'm too much of a risk; I could pose a danger to myself and others".  So I have been living on my disability check for over 11 years now; I get paid every month from the government; most of it goes towards my college, which I still plan on attending when I graduate in a few years from high school.  I keep very little for myself.

It's a pain, but it's better than nothing.  At least I get some money (and that's not counting the money I get for my birthday, special holiday traditions -- I'm Jewish --, or mega holidays like Easter, Thanksgiving, or Chanukah/Christmas).

I live with my family in Orange Park, California.  I have a mom, a dad, and two brothers, both younger; their names are Isaac and Ipswich, and they are both pains in my ass.  They drive me crazy because they can do things I can't -- like play sports, for instance, or go on the big rides at Disneyland; me I can't because I could fall out if I go into seizure-mode or have even more problems than I do now.  It's a giant pain!!

I mainly spend my days reading, playing on the computer, playing video games, playing hacky sack, playing basketball (one-on-one, of course), watching television, going to school or temple (natch), and writing stories/poems.  I am your basic loner.

I don't find that surprising:  nobody wants to be seen with the likes of me:  a tall, gangly Jewish kid who has seizures.  They've seen me throw seizures, and it's not a pretty sight, from what I hear.  I guess they think what I have is catching, so they don't want to even bother trying to get to know me or become my friend.

This is when I hate being disabled even though I look perfectly fine on the outside; on the inside, however, my brain's a mess, especially when it throws extra electrical activity that causes me to seizure out.  I have seen movies of people having seizures on television, and it's gross!  I guess I look like that:  like a dog that's been hit by a car.  It's nasty!!

I wish I didn't have epilepsy, although it's a lot better than it used to be.  I used to throw seizures every week; now I'm lucky if I have two to six a year.  Progress, yes, but still could use room for improvement; I'd rather not have 'em at all!!

I can't drive a car, get a job, or go on the big rides at Disneyland; if I didn't have epilepsy, I could do all three --  and a whole lot more.  My disability's hampered me in more ways than I would have liked it to.  I am limited in my activities, and it's wrecked my social status.

Well, I have managed to bum myself out even more, so I am going to drown my sorrows over a bowl of cereal and a can of Yahoo; maybe something exciting will happen to me today.  God, I hope so; this being by my lone self is the schitz!!

Take care and talk to ya later!  Bye!

Your friend in California, Kody.  :( 

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Reviewed by Georg Mateos 3/7/2010
More you write, more you make the world aware of children's plight, which they aren't about taking two aspirins and calling next morning.

Georg

Reviewed by Michelle Kidwell Power In The Pen 3/6/2010
Sorry he has to deal with the monster of Epilepsy I know many that have it, that can do many things, they just have to do so carefully so there could be hope for Kody, and I love the name by the way, it reminds me of Mimmi's Son, although his name is spelled with a C
In Christs Love
Michelle~
Reviewed by Mark Lichterman 3/6/2010
Sounds like one hell'of good kid. So sorry, though, that he has this ongoing problem. As usual, Karen, you give us an insite to those you write of that gives us the feeling of knowing him/her.
Your friend in Southern California, Mark
Reviewed by Karla Dorman, The StormSpinner 3/6/2010
Sadness in these lines of wanting to fit in, to be 'normal,' instead worrying if 'it' will come today ... well done, Karen.

(((HUGS))) and love, Karla.

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