Wednesday, November 9, 2022

At the Mercy of the Court

 

I was trying get out of paying a parking ticket. So I went to the city facility where hearings about parking tickets are held.

First I had to pass through a metal detector. Except wheelchairs are too wide to fit through those things and even if they could all the metal makes the alarms go berserk. So the security guy waved me around to his side and passed over me with his wand, like he was setting some sort of spell on me or trying to rid me of evil spirits.

Then I entered a small courtroom. The only person in there was a man sitting behind a large desk on high. His vantage point was such that he could look down upon anyone else in the room, like a  priest presiding over a Mass. So I figured this guy must be the judge, even though he wasn’t wearing a robe or a powdered wig or anything like that. He wasn’t even wearing a tie.

I sat before the judge and he told me to raise my right hand. I told him I was physically unable to do that. He smiled a warm, awkward smile of dispensation and moved on to the next step in the proceedings.

I wondered if this might be one of those times when my  crippledness works in my favor. Because I ‘ve noticed that playing up the cripple angle seems to be a popular strategy for celebrity defendants. When Bill Cosby got in trouble with the law, he tapped around the courthouse with a white cane and made it real clear how blind he was. Harvey Weinstein walked with a walker.  And former Speaker of the House Dennis Hastert showed up in a wheelchair.

Maybe these guys were all playing the cripple card and throwing themselves at the mercy of the court. I don’t know. But it must not have worked very well because they all got convicted.

The judge dismissed my parking ticket so maybe my crippledness worked for me. Or maybe I just presented a good case. I don't know and I didn’t ask. I just thanked him and got the hell out of there.

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Sunday, October 30, 2022

A Dog Freaked Out

 

I was taking a leisurely afternoon stroll around a campground. Coming toward me was a man walking a dog.

 When the dog saw me he freaked out. He was immediately on high alert. His ears went up like antenna. He stiffened and then did an agitated dance. And then he hid behind the legs of his human walker

The human laughed uneasily and apologized to me on behalf of the dog.

“That’s all right,” I said. “He’s afraid of the wheelchair. I’ve seen it before.”

I’ve also gotten the opposite reaction from dogs. I once came across a woman walking a big dog and when the dog saw me he started panting heavily and dancing for joy. The dog seemed bent on jumping on my lap and smothering me with sloppy kisses. The dog stood up on his hind legs as the woman pulled back hard on his leash to keep him away from me.

“I’m sorry,” the woman said to me. “His favorite person is in a wheelchair.”

That’s what I love about dogs. They’re honest. They don’t bull shit around about how they feel.

Anyway, the man walking his dog around the campground gestured toward my wheelchair and said, “It's just that he’s never seen one of those before. He’ll get used to it.”

The man and his dog proceeded on past me. The dog looked at me suspiciously the whole time.

That encounter made me feel hopeful and optimistic. It made me feel grateful for my crippled ancestors who came before me. Because that dog freaked out like a lot of humans freak out when they encounter a cripple, only the humans aren’t honest enough to admit it.  Instead of doing agitated dances, humans react in more subtle ways, like not making eye contact or building things with steps on the front entrance so cripples can’t get in.

 But life has generally gotten better. Navigating through each day is smoother for me than it was for the generation of cripples that came before me and the generation that came before them. And that’s because more and more of those cripples didn’t stay home and hide.  They went out and about and eventually humans didn’t freak out as much. They got used to us.

And I  have faith that things will go even smoother in the future for the criplets of today because I’m out and about.

I really enjoyed my afternoon stroll.


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Monday, October 17, 2022

Cripples in Heat

 

I never received sex education in school. I’m sure there are two main reasons why.

The first reason was probably because that was during the 1960s and early 1970s, when sex education wasn’t a regular feature of school curricula. But the biggest reason was probably because the schools I went to prior to college were for cripples only and whereas the idea of talking about sexuality in school was controversial enough at the time, the idea of uttering a word about sex in a school full of cripples would’ve been considered downright perverted. Hell, it was the kind of thing that might even get you arrested.

Because for some reason, some people seem to think that cripples aren’t interested in sex and it’s best to keep it that way. Maybe they think that cripples spend all of our time suffering and suffering takes up all of our limited time and energy so we don’t get around to worrying about things like getting laid. I think it comes from the perspective that sees cripples as childlike, no mater how old we are. And so exposing cripples to sex in any way is like exposing children to sex. It practically makes you a pedophile.

One thing I know about people who believe stuff like that is that they must not know any cripples very well. Cripples are probably the horniest people I know.  It seems like cripples are always in heat. You know what I mean if you’ve ever been to a large gathering of cripples, like a conference or a convention or a protest action or something, and witnessed everyone buzzing around trying to get laid.

But even though the education system didn’t tell us criplets anything about how sex works, we figured it out anyway, like all kids do. I don’t recall how I figured it out. I think that I just kept my ears open and one day it all clicked. They say that if a kid has questions about sex, they’re supposed to ask their parents about it. But those were the last people I thought about asking because I assumed they didn’t know a damn thing about such stuff. And when I did figure out how it all worked, my parents were the last people I wanted tell because I thought I knew some deep, dark secret they did know and if I tried to explain it to them they’d be all grossed out. But when  I figured out that part, too, I was the one who was grossed out.


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Friday, October 7, 2022

The Inspiring Story of Bucket Foot Bob

 

I went to a support group meeting for cripples. A new guy limped in. He clanged when he walked because his right foot was stuck in a bucket.

Even all us cripples couldn’t help but stare at him and some even snickered. But the new guy just kept walking straight on in and sat in a chair. He propped his right foot up on a stool in front of him.

The facilitator of our group said, “I’d like everyone to welcome our visitor, Bucket Foot Bob.”

Bucket Foot Bob jumped right in and said, “Actually, my name is Maurice. But you can call me Bucket Foot Bob if you want to. Why not? Everybody else does. I used to hate that name but now I’m trying to learn to embrace it.”

Bucket Foot Bob continued. “Because as you can see, my foot is stuck in a bucket. I don’t know how it happened. One night I got blackout drunk and when I woke up in the morning, there it was. And having my foot stuck in a bucket has cost me dearly in life. I have been the victim of much discrimination. I lost my job. My boss told me that my clanging around the office was too distracting for my coworkers. My wife left me. She said I wasn’t the same man she married anymore, what with my foot stuck in a bucket and all. My landlord evicted me because the people in the apartment below mine complained that I made too much noise when I  walked.”

As I listened to Bucket Foot Bob’s sad story, I felt real sorry for him, but I wondered why he didn’t just have the bucket removed.

And then Bucket Foot Bob said, “You’re probably wondering why I don’t just have the bucket removed. Well, don’t you think I’ve tried that? I mean, my foot is really jammed in there good. I’ve tried everything to get it out. I’ve tried crow bars. I’ve tried lard. But my foot won’t budge.

“My only option is to have it surgically removed. But that operation costs $10,000. I have health insurance, but it doesn’t cover bucket removal. Maybe someday we’ll have socialized medicine in this country and I’ll be able to have my bucket removed, no cost and no questions asked. But until then, I’m stuck, no pun intended.”

Bucket Foot Bob said, “So that’s why I’m here. I’m looking for a community of like-minded people who will welcome me as one of their own. I used to be embarrassed by my bucket but now I’m rather proud of it. It’s part of who I am. It doesn’t dehumanize me. It humanizes me. It makes a statement that says, ‘Yes, I’m a slapstick klutz. But isn’t everyone?’ And so, my brothers and sisters, I hope you will accept me into your tribe.”

The facilitator said, “I move that we accept Bucket Foot Bob into our group! All in favor say aye!

Aye!

The vote was unanimous!


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Thursday, September 29, 2022

Smart Ass Cripple's Disease

 

I need to hurry up and  become super famous. I’m talking about that rare Lou Gehrig level of fame.

It’s a daunting task but I think I can do it. I’m certainly motivated enough to try. Because there’s one  glaringly unachieved goal remaining on my bucket list. I want to be famous enough to have a disease named after me.

And I want to do it the hard way, like Lou Gehrig did. I feel like any old punk can take the shortcut by discovering a disease and then having it named after them, like Alzheimer or Parkinson. That seems like cheating.

But when a disease is named after you just because you have it, now that’s famous! But it has to be a certain kind of famous. Look at Michael J. Fox, for instance. He has Parkinson’s, but they still call it Parkinson’s. I’ve never heard about any groundswell to rename it Michael J. Fox’s disease. I guess he's not famous in the right way.

And what about Stephen Hawking ? He’s just as famous as Lou Gehrig, but nobody calls what made him crippled Stephen Hawking’s Disease. Maybe it’s a matter of first come first serve and  Lou Gehrig beat him to it. Or maybe you have to have the kind of fame that is free from all taint of infamy. Some people might consider Stephen Hawking to be a bit bawdy. Maybe someday something will happen  to sully Lou Gehrig’s good name. Like maybe it’ll come out that his hobby was kicking puppies. Then maybe he’ll be stripped of his disease and the title will be awarded to Stephen Hawking.

But I’m at the stage of life where a man thinks a lot about his legacy, and I really want mine to include having that which has made me crippled renamed Smart Ass Cripple’s Disease. I believe I’m crippled because of something called Spinal Muscular Atrophy aka SMA. I’ve never been officially diagnosed because it really doesn’t matter to me.  Knowing what makes me crippled doesn’t make me any less crippled.

So I’m halfway toward achieving my goal. I already have a disease. Now I just have to figure out how to get famous enough to have SMA renamed Smart Ass Cripple’s Disease. But that probably won’t ever happen. I’m too bawdy.

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Wednesday, September 21, 2022

Polio Fucking Awareness Month

 This month is Polio Fucking Awareness Month, as declared by me. I just think that considering how things have been going lately, we could all use a lot more fucking awareness about polio.

I mean, back about 60 years ago, I attended a public elementary school for cripples that was very exclusive. By that I mean that the kids who were students there were all very excluded from our neighborhood public schools.

We called some of our fellow students polios because that’s why they were crippled. They caught the polio virus.

The polios were all older than me because a few years earlier a polio vaccine was developed so no one caught polio anymore. And getting vaccinated was easy as hell. When I got mine, I just ate a sugar cube with a red spot on it. It was ridiculous. I couldn’t believe that’s all I had to do to keep from ever catching fucking polio.

I guess people don’t eat sugar cubes anymore, judging by the stuff I’ve been reading lately. I guess if you want to get vaccinated against fucking polio, you have to get a shot in the arm. But so fucking what? That sure beats the hell out of catching fucking polio.

But now I see where fucking polio is making a comeback. People in New York are catching fucking polio.

I can’t believe it! And it’s still the case that if you don’t ever want to get fucking polio, all you have to do is take the goddam vaccine!

I don’t know what the hell is going on. I hope this isn’t yet another example of the kind of shit that happens when there are a lot of douche bags running around who think not being vaccinated against anything makes them hip and cool, when all it does is put them in the asshole vanguard. And they think it’s their inalienable Constitutional right to cough in everyone else’s face like Typhoid Fucking Mary, free from government interference. I swear if anything is going to wipe out the whole human race it’ll be goddam libertarianism!

Maybe these morons will help polio make such a roaring comeback that a new strain will develop that will smash through the vaccination wall and send us all back to square fucking one. Then they’ll be real proud of themselves!

Okay but to be fair (which I really hate to do), the stuff I’ve been reading lately also says that some people don’t know whether or not they’re vaccinated against polio.

Fair enough. If you don’t remember eating a sugar cube or getting a shot in the arm, then go find out if you’ve ever received the polio vaccine. If you haven’t, then get it. Jesus Christ, I can’t believe this is even up for debate!

I hope I’ve raised a little fucking awareness about fucking polio. Thank you for your time.

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Monday, September 12, 2022

A New Labor Day Tradition

 

 I had a mighty fine Labor Day. Rahnee and I took the dogs to the park and we also took along some snacks. The weather was overcast and a bit cool but still mostly summery.

And another mighty fine thing happened that day. I’ve developed a new Labor Day tradition. I try to make it a point every Labor Day weekend to ask someone under age 30 if they’ve ever heard of the Jerry Lewis Telethon.

I’m fortunate that most of the people I’ve hired to come into my home and get me out of bed and such are under age 30. So, I’m surrounded by people from that demographic more than most old farts like me.

And I’m delighted to report that lately they’ve all said that they’ve never heard of either Jerry Lewis or the telethon.

And I feel great satisfaction when I hear that because there was a time not long ago when the Jerry Lewis Telethon was synonymous with Labor Day weekend. 

(Warning: I’m about to briefly explain who Jerry Lewis and the telethon were. If you don’t know who they were it’s better that you never do. So, skip down a few paragraphs.) Jerry Lewis was a comedian from the 1940s whose signature schtick was doing an impression of the lamest stereotype of a spaz.

Somewhere along the line, Lewis got the idea that he wanted his legacy to be as a great humanitarian who raised millions of dollars for the Muscular Dystrophy Association. Thus, he engaged in shameless pandering by hosting a 21-hour show every Labor Day weekend called the Jerry Lewis Telethon. In between cheesy, Vegasy acts, Lewis would plead for viewers to please call the number on the screen and pledge a donation to the MDA.

You’d think that would make people with muscular dystrophy, like me, very happy. But a lot of us were pissed off by it all. There were tons of reasons why the telethon reeked but suffice it to say that a big reason was that Lewis’ depiction of life as a cripple was as insultingly shallow as his spaz schtick. The telethon took the laziest approach of trying to make its audience believe that the typical cripple is as sad but extraordinarily brave perpetual child who hates being crippled and wants nothing else in life except to be cured. And we all worship Lewis and the MDA because they are our hope for being cured. But they can’t do it without the generous donations of people like you.

The telethon referred to people with muscular dystrophy as Jerry’s Kids. So, some of us formed a group called Jerry’s Orphans and on Labor Day weekends we protested around the country against the telethon. We got a lot of media attention and Lewis reacted with bitter hostility. I’m proud to say that MDA threatened to sue me if I didn’t shut up. I didn’t and they didn’t.

The Jerry Lewis Telethon is so long gone that younger generations don’t even know it ever existed. So, I guess Jerry’s Orphans won.

As we sat in the park with the dogs eating snacks, I said to Rahnee, “This sure beats protesting.”

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