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Narrative

gottalovethepandas


When heading out Monday I nearly spilled into the street because of a crack in the sidewalk at an odd angle. I clutched the handlebars, straightened myself, braked, stopped in the hot sun for several minutes until the ground stopped shifting and my feet were actually where my eyes said they were. Then I let the iPod sing out Emmylou Harris and cheered up.

You'd think by now I'd be used to this, and to a certain extent I am, but you never really get used to knowing that someone else's failure to fix the sidewalks can end up stealing minutes from your day and making you sick.

********

Found a small two bedroom one bath house online in a nearby location that just might fit my budget. I went to go look, and stopped at the edge of the street, looking down in frustration, knowing that it didn't matter what the hell the house looked like or what condition it was in; I couldn't reach it or live in it because the street it is on has no sidewalks and has a speed limit of 35 miles per hour.

********

On good days I honestly completely forget I'm sick. I feel normal. The earth doesn't shift or spin; I can sit up and stand without a single twinge of dizziness, walk without needing a cane or a wall. I still carry the cane for emergency uses, but it's more swinging it around.

I love, love the bike trail nearby which takes me through a Victorian era town and various parks and great trees and some exciting hills (yes, I can make it to Clermont, although not to any useful place in Clermont, on the trike). So on good days I mount up and head west, iPod on, looking at trees, waving at everybody passing at me and coming in the opposite direction. When I'm really lucky I get to see zebras and ostriches. I meet and chat with people.

Good day: I headed out merrily enough, stopped for water at the Killarney station, decided I was still feeling great, headed out further. It hit without warning, on a flat part of the trail; I could feel a – wooziness isn't quite the right word, but we'll use it for now.

And I suddenly realized that I didn't know if I could get back.

I got off the trike; placed myself in a prone position on the edge of the path, listened to music, told people that stopped by that I just needed to rest for awhile.

*********

I stopped to chat a couple weeks back with a man in a power wheelchair who has been trying for years to get the city of Winter Garden to focus on sidewalks. The city finally did do several repairs on Dillard Street, although they've left the several places where sidewalk users have to cross slanted driveways; if you are in a wheelchair or a trike this means that you are moving at an angle, which makes you feel as if you are going to fall into the street, and certainly prevents you from stopping until you are on flat sidewalks again. We are hoping they hit Story Road next (which is a sidewalk nightmare). So, sidewalk repairs, yay. New sidewalks, not so much.

What would also really help is sidewalking/trailing State Road 50, which right now sits as a horrific barrier to us getting anywhere. What's especially frustrating is the number of businesses on State Road 50 that we could reach/help financially support if we could get to them, or if we could cross the street. Technically, for instance, two movie theaters are within range of my trike (and we think one of them is within range of his power wheelchair) if I could take the direct route of State Road 50, which I can't. (The indirect route isn't sidewalked, either.) There's a computer repair store less than four miles off, completely out of my reach. And so on.

(I got hit by a semi-truck when attempting to cross State Road 50, to give you an idea of the problem.)

************

On medium days I'm fully aware I'm not well. But sometimes I tempt fate anyway, like a couple of weeks ago, when I felt like crap, but needed milk and eggs and fruit. Well, I told myself, you're just feeling like crap, but you're not actually dizzy. So I got on my trike, which usually makes me feel better (I genuinely love this trike) and headed down, cheering up as I went. See, I told myself. No problem. You can do this.. Made it to Publix, got a shopping cart, walked around, lifted up my left arm to reach something and came crashing down. I felt the planet tilting wildly, fiercely, to the right and thought I was going to fall off it; I could barely see.

Also, pain. The fun of having a doctor tell me that maybe I should consider knee surgery given the multiple osteochondroma and my new tendency to fall every couple of weeks, or sometimes every couple of days, only given the risks of surgery for me right now maybe that isn't the best move, and the probable best move, along with lots of stretching exercises that I need to do on the floor because if I try to do them in other positions I will fall, is to spend yet more time in a wheelchair. Note the feeling fine above. The terror of trying to get myself and my trike home through the dizziness and pain. The difficulty of reaching for ice in the freezer, knowing that sometimes just raising my arms is what will bring on the dizziness.

**********

I so, so wish the world had more sidewalks. My life is planned around sidewalks.

**********

Days go by where I realize I am feeling better, that I'm doing ok, where I start feeling guilty for calling myself disabled at all – and then it hits again. Or I'll notice some minor thing – my feet or hands swelling up (this is inconsistent and seems unrelated to other symptoms).

What's sometimes frustrating is trying to convince people, on good days, that I really am fine and I can do whatever (well, maybe not rock climbing, but I can do anything else.)

Of course, equally frustrating is dealing with people who have only seen me on good days; I keep worrying that they think I'm faking it. Hmm.

**********

Sometimes I don't even do a good job of explaining why I'm upset. It bothered me, deeply, that I was recognized at the Winter Garden Music Fest because I was in a wheelchair, and because I was brought to the attention of the cops by the truck accident and the trike theft – both of which happened because of my illness.

**********

When the fatigue hits I can sit blankly at the computer and not remember the sentence I was typing. When the headaches follow, as they do, I can't look at the computer screen at all. I'm yelling at myself, a lot, for the lack of progress I'm making on writing (as opposed to publishing.)

*********

When I'm speeding down a hill on my trike - to the point where the motor shuts off in alarm - this is totally awesome. There's one particularly great hill that doesn't have a stop sign at the bottom where I can just stop pedalling, grasp my handlebars and go WHEEE! (Yes. I often say this out loud, because if you can't shout WHEE! when barrelling down a hill on a solid steel trike when can you? Plus, sometimes I lose my hat along the way.) I gotta tell you I'm kinda sorry for those of you in cars who don't get to race down hills like this.

*********

Lots of people keep telling me to dwell on the positive. Quite frankly both my mother and T are driving me up the wall with telling me how much better I'm doing, which is true on good days and not at all true on bad days. Doing less does seem to help with bad days – except for last Friday, which was a bad day even though I'd done nothing that day or the day before.

************

So, for those of you who want "narrative," who want to understand the disabled "story," I gotta ask you: is it so hard to understand that maybe, just maybe, this sort of thing isn't the sort of thing I want to dwell on in this blog? That maybe I want to spend my time here chattering about good and bad television and movies and two of the cutest cats in the world and what they are up to at the moment (sleeping; I was kinda hoping they'd provide a nice cute story to insert here but apparently it is Nap Time and I don't think we dare excuse this) and upcoming amused stories about the Wii? That what I want to remember, to focus on, is that my life is far, far more than sidewalks and falling? That I also have friends and politics and excellent food and trees and all kinds of places in Florida that still await exploration? That it includes the Epcot Food and Wine Festival and gaming and that I apparently will be playing in an Exalted game again (I know, South Florida people, I know, but that's another post.) That I can and do do other things? That like everyone I'm hoping George RR Martin manages to finish A Song of Ice and Fire? (No, that really didn't have anything to do with the rest of this post. I just thought it needed saying.)

Look, I'm not against disability advocacy. I sense I'll be doing more and more of it in upcoming years. But asking me – or, actually any disabled person, really – to spend my time telling you the narrative of the disabled experience is problematic at best. The thing is, no two disabled people will have the same experiences. Deaf people, for instance, have a completely different set of accessibility issues to worry about. The fact that I am not confined to a wheelchair – and can actually use the trike – also means that I can't really speak for all wheelchair users, either, many of whom have completely different needs than I do. I have a chronic illness, which has its own set of needs. (And if the POTS forum has taught me nothing else it's that even POTS people have different needs.) I'm certainly willing to increase awareness, to argue for increased accessibility, and to be a public advocate for the Wonder That is My Electric Trike. (I do love that trike. That's been one of the best things of the year.) I'm spending more time on disabled forums, increasing my own awareness of ableist language, of accessibility issues, of marginalization.

But that doesn't mean I feel like spending my time writing about the Shitty and Frankly Often Boring Parts of My Life, or constantly whining about accessibility issues. Nor, for that matter, do I feel like becoming a poster child for The Cheerful And Happy Disabled Person Who Faces Her Adversities With Humor and Grace And Inspires Us All, because, let's face it, as my close friends will immediately note, that's not even remotely close to the truth. I haven't always handled my illness well at all. (Except for the trike. I like the trike.) But despite bad moments here and there (August and September had several) I've so far managed not to fall into one of my major depressions in part because, well, this isn't my life. If this illness becomes my life…

Yeah. I'm not, honestly, sure I'm mentally able to handle that. Maybe other, more mentally stable people can. But I'm having enough issues just dealing with the "disabled" label and with the restrictions on my life as it is.

So if it's all the same to you, I'd rather focus on my non-restricted life and various fun things and the terror that is Hollywood entertainment, thanks muchly. And on occasion amusing people with snark about bad movies.

(Those reading this and thinking, with horror, oh, god, she's about to go on a major Dollhouse rant, isn't she? Well, I'm kinda done with ranting for the day, but, yes, that's coming.)

This rant brought to you by commenter Marc at Feministing, among many other comments throughout the net. Thanks, I think, to troubleinchina for the link.

Comments

( 42 comments — Leave a comment )
malterre
Oct. 7th, 2009 02:26 pm (UTC)
Well the limitations are part of your life, I certainly don't have an issue with you blogging about them and in fact, you may find it useful to document some of these happenings. I am sorry they happen, I am sorry it slows you down and makes simple things hard and I'm sorry FL thinks 'civil duty' is having brochures for Disney available.
And yay for someone calling out exclusionist language
mariness
Oct. 7th, 2009 02:56 pm (UTC)
I have a genuine, non snarky question here:

Why the assumption that the only place where I could document these happenings is on this blog?

While some people did call out exclusionist language the Feministing site was otherwise full of fail, to use the current internet term.
malterre
Oct. 7th, 2009 03:26 pm (UTC)
Why the assumption that the only place where I could document these happenings is on this blog?
I don't assume that your blog is the only place-but it is the only place we see it. It's where I document because I can access it from anywhere and reference it to others. You could keep a diary but that wouldn't ever necessarily be mentioned or seen.

Feministing site was otherwise full of fail,
Yeah. *sigh* I can't help but think of the phrase
"stop making our side look bad!"


mariness
Oct. 7th, 2009 08:39 pm (UTC)
I've been trying to figure out how to answer this without throwing my hands up in the air, but the thing is, this blog is not necessarily the best place to document these things. There's a paradox - it's both a public blog, but also, a public blog which will not be read by the entities that need to read it. I mean, just here - even though this post is about a specific internet issue, no one from Feministing, which sparked the original problem, has read it. (Ok, early days yet, but still.) At the same time, because this is a public blog, there's things it probably wouldn't be great to get into. Not to mention that while I don't think there's a problem with the occasional disability post, that isn't the point of this blog, in so far as this blog has a point at all.
cardinalximinez
Oct. 7th, 2009 03:21 pm (UTC)
My thinking is similar, that this is part of your life. But it isn't your whole life. Write about it as much or as little as you want to.

There are parts of my life I talk about on my blog more than others, just because some things inspire me to write more than others. And I rarely take requests.
technoshaman
Oct. 7th, 2009 02:41 pm (UTC)
Thanks for sharing. It always helps to understand how each one's individual condition is.

Raising your arms brings on t3h dizzy.... hmmmm.... there's gotta be something there.

Here's to figuring this out, someway, somehow. And between now and then having as much damn fun as you can.
mariness
Oct. 7th, 2009 02:57 pm (UTC)
My heart does not respond properly to raising my arms, leading to a drop in blood pressure and a rise in pulse rate, which makes me dizzy and fatigued and can lead to falling.

We know what this is.
technoshaman
Oct. 7th, 2009 03:56 pm (UTC)
Sorry, somehow I missed the "we finally figured it out" thingy... did I miss anything else?

But still. Have as much fun as you can. Life's too damn short to do otherwise, handicap or no.

And +1 on Shadefell's idea of ponying up to make things more accessible. Just enlightened self-interest, that.
mariness
Oct. 7th, 2009 08:40 pm (UTC)
Postural orthostatic tachycardia syndrome/orthostatic intolerance.
lyndarama
Oct. 7th, 2009 11:38 pm (UTC)
Yeah, see, using words I can't even say isn't going to make for very interesting reading now is it Mari? Stick to words I get, like ninjas and snark and epic fail and such. Thanks. Lol.
mariness
Oct. 8th, 2009 12:53 am (UTC)
Imagine what it's like trying to pronounce it :)
lyndarama
Oct. 8th, 2009 01:26 am (UTC)
Does it make you feel dizzy too?
shadefell
Oct. 7th, 2009 02:42 pm (UTC)
For what it's worth, I enjoy (is that the right word?) reading about your disability issues because they are a part of your life, and I enjoy reading what you write period, and I enjoy reading about your life.

I live in Chicago, which is a really big town, but a lot of it is inaccessible to friends of mine who are in wheelchairs or scooters, or who can't step very high to get over curbs. Hell, on a selfish note, a lot of it is inaccessible to an able bodied person pushing a stroller. It's a serious and ongoing problem that I don't see addressed enough, although I've blogged about it at least once.

Municipal accessibility, like libraries and education, are one of those things I would totally support with a tax increase.

I agree with you about GRRM and I would also like to hear about your Exalted game. I haven't been in one yet, but a friend of mine might be starting one up when we finish our ten year long Amber DRPG.
mariness
Oct. 7th, 2009 03:01 pm (UTC)
I'm not sure when the Exalted game is starting up - presumably in a couple more weeks - but I might well be blogging about it at that point.

I've noticed that even large cities tend to focus on the needs of drivers, not pedestrians or the disabled (who are not necessarily exclusive - lots of able bodied pedestrians and bikes would like curb cuts and sidewalks, and lots of disabled people are pedestrians). I haven't been to Chicago in years, so I don't know if that's true there, but it's certainly true for Miami, Boston, Orlando, and much of DC. (Parts of DC are very accessible and walkable but that's by no means true for the entire city.)
shadefell
Oct. 7th, 2009 03:04 pm (UTC)
Although we currently have a pro-bicycling mayor and an in-theory wonderful transit system (that REALLY needs funding, and needs to be updated for accessibility), it IS extremely car centric. However, MANY of the suburbs around here don't have sidewalks at all. Which is completely nonsensical to me.
mlevins
Oct. 7th, 2009 05:24 pm (UTC)
I am one of those able-bodied pedestrians and I can affirm that sidewalks and curb-cuts are appreciated. Areas on campus here are great, but a lot of town is not as "user friendly". Since I walk to the grocery I've had people ask me why I don't use a rolling cart instead of carrying things and it is because the overpass I cross (over I-75) doesn't have sidewalks and only an 18 inch "shoulder" which makes a cart impractical (and makes it impossible for anyone using a wheelchair/motorized scooter/whatever). Things that benefit those with disability/access issues benefit everyone by making a town more "civilized" and less mechanical
mariness
Oct. 7th, 2009 09:19 pm (UTC)
I have to admit that I always liked walking around on rough or rougher territory - the closest I got to seeing the need for curb-cuts was when I was dragging around wheeled suitcases and the like.

But I do note that a lot of people who appear perfectly able-bodied (although appearances can be very deceiving here, I know) are using the Orange County Bike Trail and loving it; creating that helped a lot of people other than me. And why? Because it's extremely accessible from different roads, sidewalks and parking lots; the drinking fountains are accessible; no bumps (unlike on sidewalks I don't worry about falling over), great signs telling you how far you've gone and so on. More of this would be great.
mlevins
Oct. 7th, 2009 09:29 pm (UTC)
Oh yes,definitely! We have the Slippery Elm Trail here and I generally walk it a few times during the summer (just 4.5 miles down to one of the small towns, but the trail-head is 3.5 miles from my apartment so the round-trip adds up). Most people I see are biking or roller-blading, but there are walkers like me, too. Linear parks are a great development and it is great to get out of town
marydell
Oct. 7th, 2009 03:34 pm (UTC)
I enjoy all of your writing, disability-related and otherwise :)

mariness
Oct. 7th, 2009 08:40 pm (UTC)
Thanks :)
hummingwolf
Oct. 7th, 2009 05:16 pm (UTC)
I am glad that I don't need a trike, but I kinda wish I had one anyway.

Good post. I'm only sorry you had reasons to write it.
mariness
Oct. 7th, 2009 09:37 pm (UTC)
I think everyone should get a trike. Even people that don't need one!!!

I get a lot of people asking me trike questions wherever I go just because of the awesomeness. And the ability to carry things in its basket.
call_me_robert
Oct. 7th, 2009 05:50 pm (UTC)
I learn, and I continue to learn, how exclusive the world can be, in general. Without dialogue with people like you, I would be less aware of how I contribute to that.

I've been working on public projects lately, federally funded jobs, and the focus on accessibility is definitely there. I've learned to look at a building from different levels, different points of view. Having a sister in law in a wheelchair that was too heavy to lift was very educational, as well. The tiniest of bumps become major obstacles when pushing a 300lb person in a wheelchair...especially a person who has fallen and is completely unable to even shield herself with her arms.

I remember my brother telling me about going for an MRI, and the tech not understanding him when he told him that if he removed his hearing aids, he would not be able to hear or understand the tech at all...because without his glasses, he can't even read lips. Never failed, they would put him in the machine, sans glasses and hearing aids, and then they would try talking to him. He made those into anecdotes, funny little asides to distract from the reality of his disease, but they were still very sobering.

As a society, we still fail to account for abilities that do not match our own.
mariness
Oct. 7th, 2009 09:13 pm (UTC)
I have to note that while the focus on accessibility is often there, it's often well meaning and not at all well thought out - problems with doors/sidewalk cuts and so on. I avoid a lot of this by using a cane, but I suspect as my use of the wheelchair increases, which it will be doing starting later this month, I'll become more aware of the problems.

But, note, I do avoid a lot of problems with the cane - which is problematic because I can actually do more if I'm using a wheelchair, and I don't fall in the wheelchair. At the same time, using the wheelchair at the Imax theatre, for instance, has its own set of major issues - the major downslope/upslope from the parking lot which is very difficult to get a wheelchair up and down (luckily I have strong friends), the bump at the top of the upslope, and the cute little pathways that are incredibly bumpy on a wheelchair and make me ill. On the other hand...it's a long walk for me with a cane. Just one small example.
jesse_the_k
Oct. 8th, 2009 08:06 pm (UTC)
….and then there's where do you sit? once you're inside. 90% of the movie theaters in our area have "stadium seating," on a slant. The ADA requires them to have accessible and dispersed seating, offering wheelchair users the same variety others have in choosing. In practice, the architects leave two seatless spots on the rug on the entry level. If I sit there, the screen is less than 10 feet away, and neither my vision nor my neck accommodates that intimate an experience.

YAY DVDs! Also, in extremis, canes. (UP was worth the walk.)
synecdochic
Oct. 7th, 2009 06:13 pm (UTC)
Came via a series of links from the Feministing fail roundups, and this:

Of course, equally frustrating is dealing with people who have only seen me on good days; I keep worrying that they think I'm faking it. Hmm.

-- could have come from my own keyboard.

Without meaning to dump my issues on you, I'll just say, yes, yes, yes; a thousand times yes. There are days when I can stride happy and confident and cheerful with my head high. There are days when I can't get out of bed without enough painkiller to hospitalize someone who wasn't as acclimated as I am, and even then, it's only into the wheelchair.

You are not alone in this.
jesse_the_k
Oct. 7th, 2009 07:21 pm (UTC)
+0.8 (it's a low energy day *grin*)

Yeah, the pressure to be SuperHappyCrip is like the pressure to be SuperMom: it salves the minds of those who don't live with the effort.

I've been using a powerchair for 15 years. I still have the "ZOMG faking it!" days. Also POTS—cool! didn't know there were other folks affected like me …. runs off to find POTS forum online.
mariness
Oct. 7th, 2009 08:51 pm (UTC)
:: blinks ::

Wait - you have POTS!?!?!?!

The forums are here: http://www.dinet.ipbhost.com/. I just lurk.
mariness
Oct. 7th, 2009 09:20 pm (UTC)
Oh, and fair warning, the POTS forum, like any internet site, can occasionally be irritating.
jesse_the_k
Oct. 8th, 2009 08:11 pm (UTC)
Thanks so much for that link.

My wellness-support structure dates back to Usenet, for heaven's sake, so I have a large salt container next to my keyboard. (Especially handy for this impairment. The best part after DX was "Eat pickles! Eat potato chips!") I'm only intermittently tachy, so I guess I could have "mixed POTS/NMH."
I'm stunned to realize that the epinephrine-anesthesia issues are not only known, but actually studied.

/no more medtalk
mariness
Oct. 8th, 2009 08:50 pm (UTC)
I have mixed orthostatic intolerance/POTS, depending upon what day it is and what doctor you're talking to, although I met and overmet the diagnostic criteria for POTS, complicated with vestibular migraine, and it's marvelous to meet someone else who knows what this means. (Quest Diagnostics today hadn't a clue.)

And yeah, no more medtalk :)
mariness
Oct. 7th, 2009 08:47 pm (UTC)
I hear you. On bad days I can't get out of bed either. And of course, nobody sees me on those bad days largely because I can't see them. Only some people have seen me when I'm really bad or during/post a fall - ironically, many of these people are strangers.

And my condition is incredibly up and down, even on an hourly basis. I was really lightheaded earlier today, but now I'm just fatigued.
hummingwolf
Oct. 7th, 2009 09:28 pm (UTC)
And of course, nobody sees me on those bad days largely because I can't see them.

And of course, this simple fact is one that people without chronic illness find difficult to understand. Even doctors who should know better often Just Don't Get It.
synecdochic
Oct. 8th, 2009 02:03 am (UTC)
Yeah, this sounds horribly familiar. I'm lucky that my friends have all seen what can happen on bad days and so totally get "bad day, gotta go" ... but man, there are others who sure as hell don't.

Adorable icon, btw :)
fbhjr
Oct. 7th, 2009 09:25 pm (UTC)
It is your blog. Write what you want to write about, or not what you don't.
I understand that folks might say "tell us about this" and you'll want to do so. You are a story teller after all...
But, you can say "I'm not going to tell you that one, but I will tell you this one."

What you're going through is going to be part of you no matter what. But, there is no reason for it to be all of you or even most of you.

One of my mother's friends had polio when in her early twenties and couldn't move from the neck down for the rest of her life. She required assistance breathing 24/7. She was still a fun interesting person. A couple of times of year she was able to make arrangements to go gambling with my mother. (Jai_lai) When I was old enough I got to tag along and it was a fun time.
Her paralysis was a major part of her life that took constant management. But, it was not her.

What you're going through isn't you.
mariness
Oct. 8th, 2009 12:53 am (UTC)
Thanks :)
lyndarama
Oct. 7th, 2009 11:42 pm (UTC)
I like reading your snark, and your happy, and your sad. But especially your snark. Go for your life.
mariness
Oct. 8th, 2009 12:54 am (UTC)
I tend to think of my life as all about the snark.
lyndarama
Oct. 8th, 2009 01:26 am (UTC)
As well it should be.
jesse_the_k
Oct. 8th, 2009 08:12 pm (UTC)
And we're the richer for it.

Does snark enrichen? It's more like ginger, which adds spice … enliven? enzip?
sasha_feather
Oct. 8th, 2009 11:11 pm (UTC)
Good post!
mariness
Oct. 9th, 2009 01:08 pm (UTC)
Thanks :)
( 42 comments — Leave a comment )

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