Category Archives: Uncategorized

Why I’m unlikely to be very productive.

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(And why, if I am very productive, you might want to let me know to stop it. :-P )

I was in the hospital recently.

Photo on 2011-08-29 at 08.52

[Photo description: Me in a hospital gown in a hospital bed, with a hospital-green wall behind me, and a bunch of assorted cables and stuff behind me.]

Yet another intestinal blockage. Will not give excessive details on that area, since most people have no real desire to hear about crap and lack thereof. May also have had some kind of infection, as my white count was high.

The problem with communicating largely by typing (and using the Internet rather than the phone) is that Skype keeps logs of things you say when you’re delirious, and your friends can torture you with it later. Apparently, among other things, I start randomly advertising for Turpenoid (which I haven’t seen or used since I was about 8 years old). And that’s after I was well enough to start typing things to friends (I’ve got three days before that that have gone almost completely missing, no memory at all other than an all-too-vivid memory of an over-the-top medical procedure, and another of something that had to be a hallucination, and I sent no emails or Skype chats in that time).

Also — hospitals have to be one of the worst places to be delirious. There are too many weird sounds, sights, and smells that don’t exist practically anywhere else, and there’s an overall intensity to the place due to the amount of intense things that happen there. Once I do start remembering things, I start remembering these things:

Photo on 2011-08-29 at 14.46

[Photo shows a blue plastic robot-like thing with red numbers on the front, next to a table.]

Which I could swear are alive. And which make the most unearthly series of bleeping noises — and when you can hear them going off all over the ward, it’s just not a great way to get a grip on reality. (Even the nurses have problems hearing it over and over.)

For the most part, the care I got was excellent, which is good because I really wasn’t in much state to fight them. (Although in the one instance when they did something I didn’t approve of — a nasogastric tube — I was apparently very adamant that they stop it no later than NOW. Which doesn’t surprise me, I have such a strong objection to things going into various orifices that I can barely give myself treatment for yeast infections, and am shocked — but glad — that I didn’t just yank the tube out. It wasn’t necessary anyway, they managed to clear the blockage through much less invasive means that I won’t go into detail about. The tube is also the only clear memory I have of the first few days, so apparently it made a strong impression.)

So I pretty much couldn’t wait to get home, was even willing to put up with a drive home without a headrest:

Photo on 2011-08-29 at 17.30

[Photo description: Me in a wheelchair van, with my chin resting on my chest because I’d been sitting up too long waiting for discharge.]

When I got in the door, I heard something a lot like this (this was actually taken later, after going out for something and then coming back in again, so her reaction was much stronger than this initially):

Fey meowing when I got home. from Amanda Baggs on Vimeo.

[I don’t have the video captioned, but basically the only sound in the video is my cat making a rather intense and raspy meowing noise over and over, and me doing a mrrrrr? sound back sometimes. The video part is basically just me coming in a door and then it getting really dark.]

This, too, is not right after I got home, but is the first time I got on the bed:

Fey welcoming me home from the hospital from Amanda Baggs on Vimeo.

[The only real sound in the video is me yelling “EYYY!” when she bites me. The video itself involves Fey walking back and forth over my lap and rubbing my arms and face over and over. And then eventually biting, because she does the rub-purr-rub-purr-CHOMP maneuver when she’s glad I’m home but mad I left in the first place.]

She didn’t take her eyes off me for days:

Photo on 2011-08-30 at 12.25

[Photo description: Fey staring at me. There’s an air conditioner duct that she’s got her head poking over the top of, and her paws on either side of her face, Kilroy-style.]

So… basically, my bowels are doing much better. But I’m experiencing alarmingly similar symptoms to the ones I did last time I got out of the hospital for something like this. Which involve painful lymph glands, a mild sore throat, and total exhaustion. Which is why it’s taken me so long to write anything. And now I’m mostly writing it so that I have a way to explain the fact that I might not be up to a whole lot lately. Last time this happened, I paid no attention to what my body needed, proceeded to wear myself out several times over, and ended up with a health crash I’ve never fully gotten over since then (and which during the actual crash itself, involved the inability to turn over in bed without help). Needless to say, while I could survive such a thing again, I’m not anxious to try, so I’m obeying all my worried friends and resting.

Plus, this recent hospitalization brought home exactly how much my own carelessness about my health (I got into this by forgetting laxative several days in a row when I already knew I was dealing with a potential blockage) affects other people, not just me. So I’m not willing to continue to be as careless as I used to be. I had a lot of people worried, and one friend seriously freaking out the whole time, and for good reason — the last hospitalization for a blockage was bad, but this one was nearly twice as long, and the amount of time I couldn’t remember this time is equal to the amount of time of my entire hospital stay last time. So I’m trying to be a hell of a lot more careful, for other people’s sake as much as my own. It’s weird how it’s easier to do something for other people than for oneself.

So anyway, if I am not doing as much, that’s why. I feel pretty much like every particle in my body is individually trying to lie down and go to sleep (or to get me to do the same). And this time I’m going to listen, instead of trying to get involved in fifty projects at once, which (I’m told) is apparently my usual reaction to situations like this. And that goes for whether this is my body’s response to getting seriously ill, or whether it’s some bug I picked up in the hospital. (My best guess is it’s a reaction to something about the blockage, since it’s so identical to last time, but I’m being tested for everything under the sun just in case, since it’d be bad to miss an infection or something, and I already had four kinds of infections this summer. Yeah it’s been one of those few months.)

Oh and since most people have trouble not confusing illness with unhappiness, I’m actually fairly happy, I’m just physically exhausted. So don’t worry about me on that count.

This won’t go away just because you want it to.

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It’s kind of weird.

Throughout my adolescence, I heard a lot about trichotillomania (compulsive hair-pulling). In mental institutions staff tended liked to show off their knowledge of terminology by saying it in my presence a lot when I was yanking out hair. But I don’t have trichotillomania. It was more on the order of head-banging, a response to extreme emotional distress, not an irresistible compulsion.

I know this because I experience what’s called dermotillomania, which is just an unnecessarily long word for compulsive skin-picking. I’ve experienced it my whole life, people have made me feel about two inches tall for not being able to stop it, and I still can’t stop it 31 years on (or however long it’s been since I was old enough to do it). I almost don’t want to write this post because whenever someone actually notices what’s going on, they go to a lot of trouble to tell me how bad for me it is, or exactly how much I shouldn’t be doing it, as if I hadn’t noticed already. (It’s not always clear how much of that is actual concern for my well-being, how much is being grossed out by it, and how much is being embarrassed. It really depends on the person.)

I mostly stopped hair-pulling when my life stopped being unbearably stressful. Skin-picking is a totally different story. While it seems to increase during times of stress, it also happens at other times. I honestly suspect it’s a grooming instinct gone completely out of control — picking off bugs, except now “bugs” is anything that happens to stand out against my normal skin. Scabs, freckles, moles, pimples, whatever. Sometimes I even do it to totally normal skin.

This obviously can become a serious health problem. Besides the risk of infection, it takes things absolutely forever to heal (on top of the fact that I often have slow healing to begin with). And it’s not always just pulling off the top layer, I can dig entire crevasses in different parts of my body.

Weirdly enough, there’s a level on which it’s enjoyable. A friend reports the same thing about her parrot pulling feathers out — she’s always very interested in the feathers afterward and plays with them. The skin, scabs, whatever that I pull off create the same sort of interest for me. I stare at them, I line them up, I get especially happy about ones that are unusual sizes, colors, shapes, etc. and may keep them around for awhile. I rarely get grossed out by it, I just get very interested (interested may be a better word than happy, it’s like a form of out-of-control curiosity). The parrot also does a very similar motion to the way I run my fingers over the area of skin I’m going to pick, only she does it with her beak.

Sometimes I’m able to keep the results of this hidden, sometimes I’m not. Right now most of what I’m doing is in the parts of my ears that are either invisible to people or easily covered. (And it goes against a lot of my instincts to reveal any of that. I’ve spent way too long hiding it from people who would comment or get me in trouble or whatever. Mental institution staff welcomed the excuse to put me in restraints and get me out of the way. And weirdly, while they treated the hair-pulling as compulsive, they treated the skin-picking as akin to head-banging, or as a deliberate attempt to cause harm to my body. Two totally unrelated kinds of experiences and they got them exactly backwards. In a world where they can spin this sort of thing into “a danger to self or others” (the standards for involuntary commitment in many places) it’s dangerous to admit this kind of thing in public when you’re already prone to being locked up just because of the kind of person you are.) Keeping it hidden also helps keep other people from assuming any wound on your body is caused by this, which gets really irritating really fast, as does people insisting on sitting there watching me for it and then saying “You shouldn’t do that” every time they see it. None of these things are helpful in the least bit, they just cause unnecessary suffering.

What does stopping entail? Constant concentration. Because the moment that I let my guard down, my hand will wander off somewhere and pick something without my even being aware of it half the time. It also can make the problem come back even worse. I’m still recovering from ripping toenails out yet again after an attempt to stop. When you’re doing to yourself things that are normally described as a form of torture, you know something’s very wrong.

But “very wrong” doesn’t translate into an ability to stop this. I’ve tried just about everything possible and the moment I let up my concentration I’m back to doing it again. This isn’t the thing where “just put something else on your skin and pull it off instead” works easily. It requires so much concentration that ability to do other things can suffer in ways where it can be better for a person just to go back to doing it. It takes every bit of willpower I have (combined with increased picking in other places) not to do really serious damage by doing things like picking surgical wounds, and I only manage that by picking still other things, not by stopping altogether. And no, there’s no medication that has ever helped, even a little, and I’ve been on a lot of different medications (not explicitly for this, but if they worked they’d work regardless of why I took them).

By the way, I know there are people who consider this (and all sorts of other things) an “illness”, but I don’t. While it can always be useful for something normally considered a moral issue to be considered a medical issue instead, I don’t find it useful in my life to treat an overactive instinct as if it’s a cold or the ever-present diabetes comparison. Clearly it’s something wrong, but the only way medicalizing it would ever help me would be if it helped me pay for some way to stop doing it. And that still wouldn’t mean I wanted to medicalize it in the rest of my life. I don’t find it remotely useful to treat picking my skin more as “getting sick”, it’s just not a useful analogy for me (and in some situations I’ve found it worse than useless).

So why am I writing about this? Because it’s a large part of my life and one that very few people seem to understand to any great degree (and then their lack of understanding only makes things worse when they try to “help” me). And it’d be nice to not experience their fumbling attempts at “help”. Plus, as usual, I write a lot of things because other people’s writing has been useful to me in self-understanding and I’ve often wanted to give that back to other people when I can.

A pen, a window, a bedsheet, and a cat.

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Fey likes to hang out on the windowsill, behind a bedsheet, and cuddled up to the air conditioner duct. She was there today when I took out a pen and started swiping it along my side of the bedsheet. This is the result:

A pen, a window, a bedsheet, and a cat.

[Video shows Fey’s silhouette batting, grasping, and biting the pen through the sheet. All sounds are just the various scraping and other noises made by the activity, there’s no words.]

What a total non-apology.

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I’m not generally one to throw a blog post out there every time someone uses a disability slur. But the way this was handled is just pissing me off on multiple levels.

So a politician named Rahm Emanuel decided to insult a bunch of political activists by calling them “fucking retarded” when they didn’t agree with him on something.

Then when he realized this was going to get out, he called Tim Shriver (CEO of the Special Olympics) to apologize. This apology was apparently accepted. Newspapers are calling this an apology to the disability community.

Here’s where my brain’s starting to stall on me coming up with the language for it.

He didn’t apologize to the people the insult was aimed at.

Argh brain splitting up into pieces.

He apologized to Tim Shriver only because Tim Shriver has power and political clout and could have made his life difficult. Not for any other reason.

The slurs “retard” and “retarded” are used mostly on people with (all sorts of) developmental disabilities. If he were going to apologize to the people the terms are actually used on, he would have apologized to one or more of us, or all of us collectively.

Worse, Tim Shriver has no authority whatsoever to accept apologies on behalf of even one of us, let alone the whole of us collectively. He doesn’t even have a developmental disability, he just runs one of those primarily “of the nondisabled, for the disabled” sorts of organizations. While nobody can speak for all of us, if he’d really wanted to apologize to us, he could have started with apologizing to the heads of self-advocacy organizations. Even they couldn’t accept apologies on behalf of entire communities, but they’re closer to it than Tim Shriver is. (And why is it that when people think of DD people their minds always jump to Special Olympics?) And yet the newspapers seem to be totally buying it without even questioning. HELLO EVERYONE, WE’RE OUT HERE! REALLY!

This is just multiple layers of wrongness all piled up on top of each other. If I’ve missed one of the layers, it’s because this is really stretching my brain to write this and it hurts. Suffice to say, there haven’t been any genuine apologies going on here, to anybody. But if it’s wrong to use a slur and you genuinely want to apologize, then you have to apologize to the people the slur refers to (and directly to us, not to the most powerful person you can think of who “works with” us but isn’t one of us), as well as the people you used it on. No matter what you think of either group, if it’s wrong to use a slur then you can’t just throw a half-assed apology vaguely in the direction of someone sort-of-connected (but not actually a member) to one of the groups in question and just leave it at that.

Perfect description of shutdown

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I’m still sick. And pretty much the most intellectually strenuous thing I’ve been doing has been reading webcomics. I just happened upon this one. It’s technically about sleep deprivation. But there’s a particular stage of shutdown I get into where I’ve had conversations almost word for word like the conversation below, just not about coffee. (Clicking on the image brings you to the webcomic page it came from, on Questionable Content.)

Questionable Content strip #1477

[Image description: The comic title says “Number 1477: Read manual before operation.” Hannelore and Dora are two women standing in a coffee shop. Dora is behind the counter, Hannelore is in front of it, looking confused. Dora says, “Hey Hanners, what’s up?” Hannelore says, “What? Oh, I’m in the coffee shop now. Hi, Dora.” Dora says, “Are you okay?” Hannelore says “Oh, I’m fine, I’m fine! I hit that sweet spot at around 40 hours of bin’ awake where you feel GREAT! Can I have a cup of coffee?” Dora says “I’ll pour you some decaf. The last thing you need right now is a stimulant.” Dora holds out the coffee to Hannelore and says, “Here you go.” Hannelore takes the cup and stares at it. Hannelore says, “Um, what’s this?” Dora says, “It’s coffee. Like you asked for?” Hannelore says “How… how does it work?” while staring blankly and holding the coffee cup high at an angle where coffee begins to spill out of it. Dora, arms folded, says “You put it down on the counter, then go back to your apartment and go to sleep.” Hannelore says “Ohhhhh.“]

Thank goodness for that instinct.

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That instinct was back again this week. I’m pretty sure I’ve written of it before. Despite terrible conscious body awareness, this instinct has popped up to save me more than once. It tells me “There’s something wrong with your body. If you don’t find a way to detect and treat it, you could die or end up in the hospital.” It sounds ominous but it’s not a panicked “OMG I’m going to die AAAAAAACK!!!!”, it’s more like a calm but firm realization.

In the past, it has warned me of things like organ failure, untreated bronchiectasis (treated it’s only a little more dangerous than asthma, untreated it can kill you), and the beginnings of going septic. And this week it popped up two or three times (seemed like twice, but the first time it happened it seemed to be warning me about two separate things).

The first time it popped up recently, I was away at a recreational program. It told me to go home, not even to wait a day, just go home now. The warning seemed to be twofold: Something was going wrong with my lungs, and my body was so out of energy (from being pushed by others, but that’s another story) that I was experiencing symptoms I haven’t experienced since my last major health crash. Between the weakness and the coughing up disgusting colors of phlegm, this seemed pretty obvious, but the warning gave me the extra urgency not to wait overnight.

So I got some antibiotics ordered and went home. By the next day, my brain was actively checking out. By checking out I mean, being technically awake but not conscious of anything, or being aware only of these weird series of images that went by. It had a feel similar to past experiences of delirium, rather than shutdown or something, and during periods of better awareness I became very glad this was happening only in a familiar place among familiar people. And I was able to begin the resting that I badly needed in order to get through this in one piece.

I began to feel a little better the next day. But then, abruptly, things became far worse. I couldn’t get to the bathroom and back without falling or coming close. I sometimes felt like I was going to pass out. And I couldn’t get near food or water. I couldn’t put words to why, I would just try to drink and my head would turn away. And I felt generally cruddy and woozy. And most disturbingly, the instinct was back. It said “There’s something else wrong and this time it’s not your lungs or sinuses but I can’t tell you what it is.” Grrrrrrrr.

I told all this to someone who persuaded me to go to the ER. (Note: I nearly always have to be persuaded. A good friend describes my attitude to that place as “If Amanda got her leg lopped off, she’d be insisting she could bandage it herself rather than go there.” I’ve just got friends who refuse to give in if I say I don’t want to go there. And mostly I’m glad despite my loathing of the place.) The reasoning was that the lack of water alone would make it harder to cough things up, and bronchiectasis makes that hard enough already, and that could spiral downward fast. Plus it wouldn’t be good to pass out alone in my apartment.

Once I got there, the events unfolded in a very strange way. Normally they’ll give me IV fluids for practically no reason at all, but this time (when I was actively saying I was unable to drink) they insisted on testing my urine for dehydration. I was having too much trouble holding onto language to explain a lot of things so someone was with me explaining them. They kept demanding to know why I couldn’t drink, and the person kept telling them that autistic people can have so much trouble describing subjective experiences, that sometimes “I can’t do _____ and I don’t know why” is all you can get, and that you have to really dig and do a lot of tests if you want to find the reason, rather than acting like nothing is wrong because the person can’t name it. I was treated radically differently from my roommate, who was treated with the utmost respect. (This is common for DD people in general, including autistic people.) They even tried to get me to drink water, which is weird as usually when I’ve been given IV fluids I’ve been perfectly capable of drinking but they’d never given me water in a cup. And all I could do was wet my tongue a little and then my head turned away.

Nearly eight hours later, they came back with a way more respectful attitude to me. Why? The urine test just happened to pick up on the fact that I had a UTI. And they now thought that between a urinary tract infection, sinus infection, and lung infection, I might just have a reason to have no appetite. So they then proceeded to give me two bags of IV fluids and a prescription for yet more antibiotics before letting me go.

What scares me is what would have happened if they hadn’t detected the UTI. It’s not like they were even bothering to look for an infection. The information just popped up when they were testing for something else. And while I could tell the problem was somewhere in my torso, that’s a huge area of the body to look through for symptoms. Nothing pointed me in the direction that a UTI would have been in. And this physician’s assistant was not doing what you should do with a sick autistic person (check for all common things that could cause the symptoms). In fact, since my way of communicating my loss of appetite was so unusual, she wasn’t even treating it as a loss of appetite but rather a matter of willpower or not wanting to drink.

But somehow despite all that I’m on all the antibiotics I seem to need to be on, and seem to have found all the infections that were setting off my “get treated or you may not survive or at least may end up in the hospital” instincts. I’m just glad those instincts are there, or I would have delayed if not avoided altogether, getting everything diagnosed and treated. I certainly wouldn’t have known anything but the lung/sinus infections was causing all the new symptoms. It’s odd to have a body that won’t tell me basic information half the time, but will tell me “You’re in danger, get help NOW.” I wish that simply communicating this instinct to a doctor would result in getting tested for whatever things seemed likely. I think I could do that with my GP, but not with some of the random people you get in the ER. And trying to negotiate all this while disoriented and confused is just… gah, I’m glad it somehow worked out because I honestly don’t understand how, especially given I wasn’t “all there” during times I needed to be communicating clearly.

By this point I’m pretty wiped out and still having appetite problems, but I’m feeling a lot better. I don’t need my bipap while awake anymore, I can get around a little using my old crutches for stability, and my brain is no longer randomly checking out, nor do I feel like any moment my surroundings will burst into a Disney Acid Sequence (warning: the link is to TV Tropes and may suck you in and spit you out twelve hours later). And I’m hoping we caught everything the instinct was talking about.

Words that bite my brain

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I can’t stand these words.

Words that cause a range of cognitive pain for me.

At minimum, there’s a sense of them pulling me diagonally. I may understand the meaning, but they still strike me wrong. If I do understand them, they cost cognitive effort to figure out. Not the kind of effort that anyone should be expected to put into understanding things that are difficult for them. That kind of effort is effort I’ve already spent understanding regular words. This effort is beyond that and is destructive to my ability to do other things I have to do. Have to as in have to, not as in “feel like doing”.

Then the worst of these words. There is little to no understanding here. It feels like a miniature explosion in my head every time I read them. I can’t find another way to put it. And the pain they cause, although not physical, is quite intense and feels like a cognitive version of nerve pain. Anyone who’s had serious nerve pain will know how bad that is.

Most of the words are ones I rarely if ever use. But some of these are words I can bring myself to use, some of the time. Some are even words I’ve coined. That doesn’t seem to matter though, they still hurt my brain. So don’t assume that my using or even coining a word means it being easy for me or expecting everyone to like or use the word.

I will say that these are words commonly used in communities that call themselves “social justice” related. The reason I put “social justice” in quotes is that, as a word in the midrange of mental pain levels, I can’t quite bring myself to write it down as if I were using it. That would make it look like I know what it meant. (Not that that always stops me from using a word, but it often does.)

There’s a reason, though, that I’ve abandoned the idea of writing most of these words down in public, in this post.

Because when I’ve brought it up in the past, I’ve gotten a variety of pretty offensive responses.

People patronize me.

They treat me like not knowing these words is a sign of some kind of privilege.

They openly brag about their extensive knowledge of the subjects the words refer to.

They assume because I can’t handle or don’t understand or outright get pissed at the existence of a certain word, then I can’t possibly know anything about the subject the word is supposed to refer to.

They try to patiently teach me the meaning of the word, ignoring me whenever I try to explain that this doesn’t work with this kind of words.

They suggest that I don’t like the words because I don’t experience the kind of oppression that the words were built to describe.

They sigh and roll their eyes and get scornful. Because I’m obviously just some noob who wants everything explained to me (possibly because of an overdeveloped sense of entitlement).

Often their reaction is more than one of those things combined. “Well I for one totally know what the word means. I’m an expert in that area. I guess you are just too privileged to understand. But here, let me try to explain anyway. (As if I should have to.)”

I know it’s not about that, though, because often I know what the word is trying to refer to. I just can’t connect that meaning to the word without a lot of effort and pain. And the connection is never really complete.

Let me just say straight out that I would rather deal with one person who gets words “wrong” (and may even use lots of words deemed offensive due to not being able to keep track of that kind of thing) and may sound “clueless” to the social intricacies of communities or the meaning of words, but has good ethics and a grounded sense of reality; rather than a hundred people repeating all the right words with only a superficial take on the issues at hand and a tendency to want to blend in more than to solve real problems.

I only decided to write this post after seeing other people mentioning their own problems with this kind of language. Not identical problems, but clearly I’m not the only one who finds these words difficult. I’ve seen suggestions that these kind of words can shut people out of the discussion, even if that wasn’t the intent. I have to agree. I also saw someone who had an extreme emotional reaction to a similar set of words, and they wondered if their brain was responding to something real… like something about how people turn words into some kind of rigid ideology, and I have to wonder about that too.

[Note: I may be unable to quickly process comments starting very soon and then for a couple weeks minimum, so please don’t be alarmed if your comments don’t show for awhile.]

Wheelchair coverings

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It’s getting really hot out. And for a heat-sensitive person there’s very little worse than being in hot weather in an all-black wheelchair. So I decided to cover as many surfaces as possible on my new manual chair, with a very much non-black fabric. Here are the results:

My manual wheelchair from the front.

My manual wheelchair from the side.

[Photos show a manual wheelchair, first from the front view and then from a side view with the seat tilted back. The base of the wheelchair is purple. The seat, back, headrest, armrests, thigh guards, and leg rests are covered in a fabric that’s light blue with white clouds and white butterflies, and glitter.]

I ended up covering the cushion, the back rest, the headrest, the armrests, the thigh guards, and the leg rests with this fabric. I am completely unable to sew, so I did this all with scissors and an entire pack of safety pins. (Being careful when doing the cushion, that I poked the safety pins into the outer fabric cover, not into the gel.)

This is how I look right now:

Fey on my lap, with me looking exhausted.

[Image shows me and Fey. I’m flushed and generally inert-looking, and Fey is standing on my lap looking to the side.]

Because I’m completely exhausted to the point of nausea, which is never a good sign (although I wasn’t feeling great when I started). The bipap I’m using for central/obstructive sleep apnea has certainly increased my stamina, but not by this much. I’m now resting in order to get up the stamina to get in bed, which is another bad sign.

When widgetry and identity politics consign people to living hell.

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Here’s an article, I got the link from NOBODY PASSES, Darling.

The article itself is Rich Man’s War, Poor (Gay) Man’s Fight. An excerpt (a long one because my brain won’t let me figure out shorter ones):

The President of the United States, a former Constitutional law professor lately suffering amnesia about the presumption of innocence, declares publicly that “he broke the law.” The United Nations Special Rapporteur on Torture, Amnesty International, and the American Civil Liberties Union express grave concern about the conditions of his imprisonment, and the spokesman for the U.S. State Department is forced to resign after calling it “ridiculous and counterproductive and stupid.” A letter signed by 295 noted legal scholars charges that his imprisonment violates the Eighth Amendment prohibition of cruel and unusual punishment and the Fifth Amendment guarantee against punishment without trial, and that procedures used on Manning “calculated to disrupt profoundly the senses or the personality” amount to torture.

The National Gay and Lesbian Task Force, the Lambda Legal Defense and Education Fund, and the Human Rights Campaign, having invested millions lobbying for “gays in the military,” have no comment. Of course not. Bradley Manning is not that butch patriotic homosexual, so central to the gays-in-the-military campaign, who Defends Democracy and Fights Terrorism with a virility indistinguishable from that of his straight buddies. He is not that pillar of social and economic stability, only incidentally homosexual, who returns home from the front to a respectable profession and a faithful spouse and children.

No, Bradley Manning is a poor, physically slight computer geek with an Oklahoma accent. He is, let us use the word, and not in a negative way, a sissy. Having grown up in a dysfunctional family in a small town in the South, he is that lonely, maladjusted outsider many gay people have been, or are, or recognize, whether we wish to admit it or not. He broke the law, the President says. And he did so–the liberal press implies, trying terribly hard to temper severity with compassion–because he wasn’t man enough to deal with the pressure. He did so because he’s a sissy and he couldn’t put up with the manly rough-and-tumble that is so important to unit cohesion, like that time three of his buddies assaulted him and instead of taking it like a good soldier he peed in his pants. And then of course he was so embarrassed he threw a hissy fit and sent Wikileaks our nation’s most closely guarded secrets, like some petulant teenage girl who gets her revenge by spreading gossip. This is, of course, the classic argument about gays and national security–they’ll get beat up or blackmailed and reveal our secrets. And NGLTF, Lambda, and HRC, with their impeccably professional media and lobbying campaign, based on the best branding and polls and focus groups that money could buy, have effectively demolished that insidious stereotype.

They have demolished it by abandoning Bradley Manning.

It took a lot of cognitive effort to cut and paste those links, and then choose, cut, and paste the excerpt, not to mention find the words to put in the title and introduction. Yeah, it’s one of those nights. (So far. You never know when the weather in my brain will change without warning, but right now it’s lousy writing weather.) I had wanted to do a post with several links to different articles I’ve found recently, but I realized I’d be lucky if I got this one post written.

Oh and I didn’t write this post to start a debate over whether what’s happening to this guy is justified, so if you feel the need to justify it, do it on your own blog (or on the blog of someone who doesn’t mind hosting such a debate). I wrote it because these sorts of power dynamics among “activist communities” (and indeed the whole structure of such communities) ruin real people’s lives. And so does the use of widget-based morality — something I’ve planned to write more about why it works that way but haven’t had the opportunity. And of course the power dynamics and the widgets are entangled in ways that more than guarantee this level of sheer tangled bassackwardsness.

Spider Smiles

Standard

It’s always “fun” to wake up to this kind of spider-smile leaning over your bed:

A spidery-looking Other Mother leans over Coraline with a creepy smile.

[Image description: From “Coraline”, a stop-motion movie. The main character, a girl named Coraline, is standing there as her “Other Mother” (a spider-like monster pretending to look like her mother, but with buttons for eyes) leans over her with a creepy smile.]

…and then have to let the person, among other things, wash your private parts. And to know you pretty much have to let them, because you don’t want to get a reputation for rejecting people for no reason (or “not good enough” reason).

And no, it’s not a sexual kind of creepiness. It’s more like a weird power dynamic, where the person thinks everyone loves her and that she can do no wrong, while running roughshod over everyone, human or otherwise, even above their vocal objections to her invasiveness. You can explain it to her calmly, or shout “No! Stop! Stop NOW!” and all she’ll do is giggle and keep doing whatever she’s doing, whether it’s barging into your bathroom while you’re on the toilet, trying to touch a pet who doesn’t want to be touched, or otherwise violating people in various ways. After awhile the giggling and smiling gets more and more creepy, and happens with more frequency the more you try to assert yourself. I think the spider-like component — which another client of hers has described as an “I’m gonna eat you” smile — comes from the tendency of people like this to “feed on” imaginary gratitude and the like (see My Contaminated Smile for something similar).

This kind of behavior is especially damaging to anyone who (like me) is so used to these boundaries being crossed that I often don’t think to defend them. As Dave Hingsburger explained in a video I saw once, that leaves us open to serious forms of abuse because abusers look for people who don’t push back the minute we experience invasion. It also erodes the boundaries between your own home and institutions. It’s a lot more damaging — especially after each “little instance” begins to pile up into something enormous — than any one instance would look on the surface to most people.

And I suspect a lot of people think it doesn’t matter when done to people who aren’t going to experience a whole lot of bodily privacy anyway. Wrong. I used to think it didn’t matter so much because I was used to lacking privacy and was very late to develop body modesty anyway, until I heard that explanation about how being “used to it” primes us for later abuse. Ever since then I’ve tried to create privacy in various ways when possible, even though I’m not used to it and don’t automatically “feel” some of those first levels of invasion the same way other people do. (I’m trying to build up to where I do feel them, with some success so far.)

One time she explained to me she was incapable of abusing power, because she was a Christian. I would love it if the world really worked that way (for any religion or lack thereof). It would be a much better place. But meanwhile she goes merrily on her way, dispensing really disturbing (but not technically against any rules) experiences with a big creepy smile and a chirpy sing-song voice.