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Showing posts sorted by relevance for query danny. Sort by date Show all posts

21 November, 2009

They hate you. Yes, you.

I always think about Danny, who was not really named Danny. It's too bad I can't use his real name because it's one of my favorite names. I'm sure he's forgotten me but I can remember his name, his face, his favorite subway train, and the words he made up.

He was a kid I met this summer at the school where I interned. I have written about him several times, sometimes at length. And although he was my favorite kid at the school, that isn't why Danny is always surfacing in my mind, tiny in his big t-shirts, flinging himself around and reciting things.

It's through Danny that I found out for sure, this stuff is about me.

Because the first thing people use on us is always, "It's not about you." When I was a kid, when I first started reading about autism rights, it was so instinctive: of course it's wrong to say "cure autism now." Of course it's wrong to say autism is a tragedy, a disease, it's wrong to give kids electric shocks, it's wrong to say you thought about killing your kid in a video about eliminating autistic people from the gene pool. Like Sinclair says it's wrong to mourn for a living person. All this stuff was plain and clear and bright, and I was autistic, and I was being attacked.

Right?

Well, not to anyone else.

Because, of course, if I told anyone I was autistic, they said I was lying, or I had a different kind of autism that made me smart and talented, so I wasn't like Those Kids, the kids who needed to be cured. And that I should think about their parents, about the money and time to care for a person like that, about the dreams that are shattered when your kid is really autistic, not smart autistic, the real kind. So in my late teens when I put myself through my paces, when I figured out my deficiencies and set myself to systematically eradicating them, one of the deficiencies I eradicated was my use of the word autistic. Because you shouldn't use words people don't understand. And you shouldn't use words that will make someone feel bad, someone who has a kid who's Really Bad, Really Disabled. Because you're not that.

And I met some autistic kids and they were not much like me, and I didn't know to apply what I knew about myself to them, because I couldn't see what they were feeling inside. But I liked them. Then I met some people with intellectual disabilities and I liked them too; after a brief nervousness because some of them looked so different from me, and made noises I didn't understand, it was easy to like them. They were people who liked things, some of them the same things I liked. I could see that they weren't on the surface very similar to me, but I liked being around them almost more because of that, because it made me feel happy and chastened to misjudge them again and again. To be proven wrong when I thought I could quantify them just because I knew more words.

So by this point, I was pretty much sold, even if I wasn't Really Autistic, on the idea that people with developmental disabilities matter. Because I was around them all the time and it was obvious they mattered. But still, I felt my position was that of an outsider, an ally. I had opinions but I didn't necessarily feel that I had much right to talk about them; I didn't feel I had as much right as the parents or teachers of people with developmental disabilities.

And then I interned at this school.

And I started out thinking: wow, ABA is so cool. I've heard negative things about it from other Not Really Autistic people, but who am I to talk about what these Really Autistic kids need? They can't even talk. They might bite themselves or something. What the hell do I know about that?

And then I met Danny and the other kids in his class. High-functioning kids. Verbal kids.

Tony, who had been nonverbal a few years before, was incredibly hardworking and sweet. When he went into the school director's office and turned out the lights as a joke, I laughed, but she said, "Tony. Look at my face. How do you think that made me feel?" She stood there looking grim until he apologized.

James was stressed out and upset; one of his teachers leaned towards him, staring fiercely into his eyes, talking with cold, strained-sounding words, the kind of voice I called "static" when I was a kid. James looked scaredly back at her, wriggling his hands around in his lap. "James," she said. "I know you're upset. But what you're doing with your hands looks silly." This boy, all the tension in him being channeled into something harmless, something she had to look under the table to see. His tension was silly. His discomfort was an inconvenience. He was eight or nine years old.

And Danny with his words. "Danny's an interesting kid," the school director told me. "He likes to be in charge." Danny and I were walking, holding hands, and when I responded with concern when he told me he was tired, another teacher told me, "He's playing you." It's true that Danny was a bossy little boy; when we played restaurant, he replied, "No, we're out of that" again and again until I ordered the food he wanted to pretend to make. And his love of subway trains spilled out everywhere. He was supposed to write a story about a sad princess, and he did, but half the story was about the princess's friends taking her on the subway to cheer her up. He was supposed to write a crossword puzzle and the clues were things like, "Transfer is available to _____ North." The school was full of subway maps, since many field trips involved subways, and Danny would sometimes just lean over a desk, pressing his face into the shapes and colors, whispering his favorite schedules to himself.

Danny just liked words. When he was using his special words, the weird words he scrounged for or made up himself, he would find himself jerkily hopping across the room, speaking in a squeaky voice, his small face tense with excitement. "Presentation" was a weird word for movie, "document" was a way to talk about the letter he had typed on the computer for his parents. "I went to the barber," he said when I commented on his newly short hair, and then, with a rush of joy, "but I like to call it the hair shop!"

I like words too. It was hard to watch Danny's teachers nudge him, sit down with him, say, "Danny, the word 'presentation' is a little weird; you need to say 'movie.'" It was hard to watch the way they looked at him, pointedly, until he stilled his hopping and lowered his voice to a more standard pitch. When Danny found out my middle name is Wood, he completely tripped out on it, hammering pretend nails into my stomach and giggling, "I'm gonna build something out of you!" "Danny," a teacher said, "don't be weird. You and Amanda were talking about names."

It was the word weird. Nothing foreign my whole life. Tracing words and shapes in the air, crossing myself, my mom asking me a lot of questions, "Have you been feeling the urge to do that lately? Why do you do that?" with so much static it was clear I'd better keep my hands as still as possible when she was around. Running jerkily up the stairs at school, I couldn't help myself until I was fifteen or sixteen, despite the older boys laughing to each other--"is she trying to race you?" Movement just consumed me that way. And being a thirteen-year-old who said "suppose" and "quite" when no other kids did. Just loving words too much, finding it hard to stay away from the strange ones. And getting too excited. Being weird is not that alien for me.

So my divisions broke down a little, because I was watching a kid just like me, and I was learning, in very specific, qualitative terms, what they thought of people like me. I was so nervous about keeping myself still and using the right words because I thought they wouldn't let me intern there if they knew I was actually like Danny, that I didn't think he was weird at all. All of Danny's teachers had been taught to grimace and say how annoying it was when he talked about trains. They watched The Office, but they never ever laughed when Danny told flat, self-referential jokes on purpose, twisting the ones he had been trained to say. I thought Danny was funny. Every time I talked to him I felt nervous about doing something that his teachers would think was wrong, and I also felt bad about perpetuating the attitude he was being taught, that none of the things he loved mattered.

So from specific to general, from Danny to James and Tony, to Max and John. John's teacher made him walk, in stiff, clean steps, and if he started doing anything that looked like skipping or jumping, she grabbed his arm, said "No," forced him again and again. Max liked to move his arm in circles while he was watching TV, so he was hauled off into an office, pushed down into a chair, had mouthwash forced into his mouth while he cried. They told me they were narrowing it down, he was moving less and less. Max and John didn't talk. James and Tony didn't talk as well as I do. But I move too much, and I move wrong, especially when I was a kid, and in that school I saw what they do to kids who move wrong.

I realized that, actually, a lot of it was about moving wrong. Or talking wrong, if you could talk. Or just taking too much initiative--wanting to make up songs, like Danny did, or playing a practical joke, like Tony did. That these kids looked and acted different and the school wanted to control them and make them as still and docile as they could possibly be. Watching them treat hopping, rocking, and neologisms like you'd treat a bomb on an airplane--it was like being at summer camp with a kid from the south, sitting in a car uncomfortably while he said he'd kill a gay person if they ever came near him. Wanting to say, no, it's not anything important; I'm like that, see? But I didn't talk in the car and I didn't talk in the school.

This is too long. It's hard to even explain it. I just have to say, for the millionth time, that this whole functioning level thing--yes, it matters in certain ways. I can buy and cook food for myself, while a severely autistic person probably can't. I can hide the way I move and talk better than other people can. But this doesn't really have much to do with politics, because when people claim that "cure autism now" and the disease and the Judge Rotenberg Center are not about me, well I beg to differ. The only reason they're not about me is that I'm old and verbal enough to not be vulnerable to that kind of abuse. They would be all too happy to practice it on me if they could. Autistic people do not get abused because they are low-functioning, they get abused because they do weird things.

So, the old-school ABA trials? With Lovaas?

This is a kid getting an electric shock:



This is why:



If you were in the wrong place at the wrong time, the wrong age, the wrong functioning level, this could be your life. This what people like them think about people like us.

21 December, 2009

OF COURSE I UNDERSTAND THE IMPORTANCE OF PASSING

Today my dad brought me to meet his friend who is on the board of a Down Syndrome organization and a music school for people with developmental disabilities (mostly Williams, I am sort of obsessed with Williams thanks to my crush on Jeremy Vest from How's Your News). It was really great to talk to her about disability stuff, and as with most things that are great there's not much to say about our conversation.

However, one thing kind of struck me (not really her fault, but it just struck me and made me think about a particular DD strawman). Basically I was talking about my experience at The School and how alienating it was for me as a person with ASD to see kids being corrected for stimming, talking weird, etc. I wasn't censoring myself because she mostly works with intellectual disability stuff, and that culture is much more comfortable with people looking and acting weird. (I think this is tied in with the whole privileging of ASD among developmental disabilities, and is an interesting example of how having higher status can make things worse for you in some regards; but I have a thousand words to say about that topic, so I'll save it for another post.) My frustrated spiel about The School kind of built and culminated in, "So, the thing is I'm interested in ABA, but if I'm applying to work at a school, how am I supposed to tell if they stop kids from flapping their hands or if they care about things that are actually important?"

My dad laughed. "Well, you certainly have an opinion," said my dad's friend.

She didn't seem offended or anything. But then she started telling me how they work on teaching the students at the music school to behave in a socially acceptable way. She said for example that when they have jam sessions at school, it's okay for the students to clap their hands and cheer for each other in the middle of performances; but when they go and play in other venues, they're not supposed to do that. The school tries to train DD people for careers in music and that kind of behavior will get in their way.

This seemed legit, but I didn't know how to process it as a response to what I had been saying about The School. Finally, I said, "Well, I feel like there's a difference between teaching someone to self-monitor, and just saying, 'You're not allowed to do this thing that you like to do,' because that just makes them dependent," and she said "exactly, self-monitoring is really important."

Right.

When I was at The School, I helped organize this directory of New York autism resources that they were hoping to give out to parents. When I printed out the final document (as Danny would say), I put an image on the title page, something I had found on Google which represents a computer term I don't understand:



When I look at this picture, it makes me incredibly emotional. It's so beautiful and that's just what I want for Danny and myself and other people with DDs. This picture makes me think of a time this summer when I got really lost in the subway system at night and I ended up having to ride all the way out to the Brooklyn Bridge and then come back. (I live in Connecticut so I was trying to get to Grand Central or 125th Street so I could go home). My phone was dead so I couldn't call my mom, and every stranger who attempted to give me advice made things worse, so I stopped asking and just gave up and decided to do things the longest way possible.

So I'm waiting for the train to take me back to Grand Central, and it's been a really hot day and I haven't had much water and in addition to screwing up my processing and getting me lost in the first place, this is causing me to have a headache. And I'm just standing on the platform at eleven or twelve. And I start moving my hand down by my side, back and forth, hard, really swinging it around. And the pain in my head goes away.

And I am thinking of Danny of course, because I saw him today; and I've been thinking how Danny will never get lost in the subway system because he knows it all. But also, as the pain stops, something I've only learned recently, that it really is okay to move my hands sometimes, and that it helps me a lot--I just think, shit, I hope that Danny figures out that it really is okay to move his hands, no matter what they tell him.

I don't have time to finish writing this and it's kind of fucking me up but basically the thing is, I'm a passing person with a DD so it just doesn't make sense to imagine that I don't understand the value of learning socially acceptable behavior and that I think it's a cool idea to encourage DD people to go around vocalizing and rocking back and forth in job interviews or at the movies. If/when I have a kid with a DD, I will of course advise my kid on what is prudent behavior.

But telling someone not do things that are good and/or fun for them, things they usually end up sometimes doing anyway, is just sort of ridiculous! And mean. And impractical. And if you have a school that is built on the principle that completely ordinary but odd-looking things are a Big Problem, then I have to imagine that you just don't think about developmental disabilities in a very practical way, and I have no idea what you would make of a person like me.

27 August, 2010

Run Forest Run: about movement and love

The summer after my freshman year of college I took all these pictures and posted them in the Asperger's LiveJournal community.

picture of me: a 19-year-old white girl with green hair and headphones on, flapping her hand and staring into space. The picture is blurry and the sun is shining on her hair, giving it a supernatural or angelic quality.

another picture of me flapping and looking serene. The hand is flapping so fast it's not visible.

flapping with headphones on and a serious expression

jumping into the air and flapping arms, again because of the light and blurriness it looks sort of angelic.

I took these pictures because I didn't know what I looked like when I was stimming and I assumed it probably looked scary. As soon as I started taking them, I realized it looked sort of cool, at least in pictures, so I took a lot more.

Before, I didn't have an image of what a person who stimmed could look like. I'm not saying I was raised to feel terrible about stimming because I wasn't really cracked down on by teachers and parents like some people are. But it was sort of similar to how I felt about being queer--I either heard vague negative stuff, or silence.* I saw people on the Internet saying it was okay but I had trouble applying that to my real life.

The next summer, I wrote this piece: Functional Stimming. It was mostly a reaction to anti-stimming attitudes at the school, but I tried to approach the issue of stimming in an objective and accessible way. I took pictures of myself stimming and described how I felt about stimming, and I talked about two people I knew who stimmed, and included pictures of them.

Towards the end, I said:

I don't feel great about the way I stim. I wish I could stim the way Clayton does; it seems so natural and unselfconscious, just an intense expression of his feelings. I feel like I have a stimming habit, like I binge on stimming. It feels like an explosion and I feel worn out afterwards.

I remember other kids making fun of me for shaking my knees back and forth in class and compulsively touching my nose while I was reading. I don't know if that's how my stimming got driven underground. I just very much wish that instead of being this giant, dramatic, embarrassing thing, stimming could just be part of my life...

I just went and walked in circles for a few minutes trying to get my thoughts together. That was really nice. That's the kind of stimming I would like to do--calm. Something that makes my thoughts make more sense instead of ratcheting them up to fever pitch.


That summer I also made some videos like this:



One night I got stuck in the city with a headache and some general spaced-out-ness and was really screwed in terms of finding a quick subway train back to Grand Central. Last summer was the first time I really started understanding subways at all, and I'm still not very good. So I ended up riding around a lot and it was really late at night and I remember being really proud because I knew I would eventually get home even though it was hard, but I also was feeling unpleasant in other ways because it was loud and hot and I had a headache. I was thinking about Danny because I was seeing him every day and he loved subways. Thinking about Danny always made me think about passing and stimming, so I started stimming while I was waiting for the subway and it made me feel better.

And I had a horrible year in general and I became much more conscious of times when I needed to flap my hand by my side or scrape my palms along the edges of tables or step my feet around in circles. It was weird because things were so awful and in many ways I felt scared because I was letting go of many standards for being normal that I'd previously held and I think I worried that if I wasn't holding myself in place, I would somehow wake up one morning and be nonverbal or something like that.

At the same time, when I went back and read Functional Stimming, it seemed that all the problems I'd had were a lot better. Stimming had become something wholly neutral or positive. It wasn't always this full-body thing that exploded out of me unconsciously when I was alone, and hyped me up more than I wanted. It was just a tool and a joy.

I'd also started to feel differently about the way I hold myself. I think it's called posturing because when I say I move stiffly I don't mean I am stiff, or something, but that I find it nice to stick out my arms and legs and hands.

picture of me: a 21-year-old white girl standing with legs very stiff and stuck together, arms very stiff and extended as far as possible down by sides, hands in fists, face stiff and clenched.

This is an overdramatic version of what I mean, because I'm doing it on purpose, but you get the idea. It especially affects the way I walk when I'm really at all excited or at all nervous. I just move my legs very stiffly, which probably is hard on my feet or something, but it feels really nice. If I try not to look different, it gets even worse because I'm nervous, and it ends up just being in the legs which are moving really mechanically. (One time Amanda Baggs wrote a post which in part was a description of how she notices ASD people based on how they walk. Some of this explains well what I'm trying to talk about.)

I guess this spring it occurred to me that I'm not the only person in the world to ever hold my hands differently and I started thinking about what I was afraid of looking like. There was obviously something I was freaking out about and trying to avoid but when I thought about it I realized it just looked like the way some people with ID and ASD walk and hold themselves all the time, and it also looked like some people with cerebral palsy. Once I started thinking of it that way, it didn't seem like a bad way to hold myself, because I associated it with other people and not just me being different by myself.

Now instead of trying to walk normally and then occasionally walking really stiffly, and also having these huge full-body stim explosions when I'm by myself, I just walk in a way that is more uneven and "posture"-y and I tend to kind of burst into a run more and sort of have stiff legs and move them around in a jumpy way. Not that I don't jump around on my own sometimes when I'm excited, but it doesn't feel like a huge problem that takes up a lot of energy, it just happens from time to time. And I don't feel bad about holding my hands in a stiff/curled-up way that feels good.

Of course I have criticisms of the camp where I worked this summer because you should always be aware of flaws, but it was in many ways very cool and very different from The School, because we weren't encouraged to think of ourselves as socially separate from and superior to the campers. Staff got involved in campers' interests and senses of humor; we weren't trying to get them to copy us. To the extent that we were trying to do stuff, we were trying to make sure they liked us and had a good time with us.

This was apparent before the campers even got there, just from the tone of our training. I was already feeling pretty happy and safe a few days into orientation, when we were going back to our cabins for a break. I felt excited and as often happens I ended up running for no discernible reason. Another counselor saw me and said, "Run Forrest run!"

I have had people make shitty comments about the way I run, and although this person was being friendly I can still imagine that I might have felt embarrassed and angry to have been "caught" doing something like that. But I guess since Forrest Gump is in fact disabled, even though she probably wasn't trying to make a comment about me looking disabled, I just processed it calmly in my head: "Forrest Gump is disabled and I'm disabled and I reminded someone of Forrest Gump. That makes sense." In the moment it made me feel good.

I also just remember dancing a lot (I had never danced before) and being excited and squealing and posturing and tripping over things because I was running around so much, the whole time I was at camp. It wasn't anything to be ashamed of because I was doing my job properly, and there were lots of awesome people around who also squealed and ran around a lot and flapped and made motorboat noises. There was a moment when I remember being really excited and happy in a really disabled-looking way in front of the whole camp, and I felt sort of transcendent and like I was going to cry. It was a weird sensory experience too, and just in a lot of ways one of the best moments of my life.

One time in seventh grade, I remember walking around with my shoes untied and not caring what other kids said until one girl said, "You look like a boy with your shoes untied." Then I immediately tied my shoes. Since then I've gone through periods of really really wanting to look like a boy, and even though I don't feel that way anymore I generally would find it cool to be told that something about my appearance looks like a boy. I tie my shoes now, because I would probably trip over myself when I start RFRing, but I'd like to think I own the possibility of looking like a boy. And I want to also own the possibility of looking disabled.

This is a pretty nice thing actually. I don't enjoy passing. Just kidding, I love passing. Just kidding, I hate passing. I mean I don't know. I am likely to think people who are visibly disabled have it worse, but I sometimes really wish I was visibly disabled and sometimes I feel like the fact that I'm not is what has caused basically all my anxiety/dissociation problems.

I have a lot of what I think are probably normal issues for women my age--basically, thinking that I'm horrible-looking and combing Facebook for pictures of myself and even if it's just a picture of my arm totally flipping out about how my arm looks horrible. Or maybe I have it on a level that isn't normal. I just look at pictures and think I'm smiling differently from everyone else in the picture. My face is bigger or smaller than theirs. I'm holding my legs differently. My hands look stiff. No one in the picture looks like they're my friends. I look like I'm just lurking in the background.

I just engaged in a bunch of this yesterday so I'm certainly not claiming that I feel great about myself now but I think that my feeling shitty about myself has been reduced to a more standard level. I also feel like I have something to move towards the way other people do when I think about how I'd like to look or how I'd like to be. Because I have images of people who look like me.

This is the reason I have trouble identifying as just Autistic instead of developmentally disabled, just because lots of the people who have led to me feeling okay, and feeling like a kind of person instead of just something unclassifiable, have been people with ID and other disabilities. I've talked about this a lot. But I just realized the other day that things are feeling so much better so I wanted to tell you some more.



*I'm sure my parents would take issue with this, especially in terms of queer stuff. I know that most people have it much worse but the thing is that most of the messages I got about queerness and DD were either mildly negative, acted like it didn't exist, or were very long-sufferingly tolerant (like my high school). Which isn't terrible but does make it hard for you to actually form into an adult because you feel uncomfortable/depressed about a lot of the things that you are.

11 February, 2010

heroes

1. Danny for not being modified.
2. Henry Darger.
3. Francisco Hernandez Jr. for not being made of stone.
4. Noah, a boy I went to camp with when we were 15 and 17, who would carefully and nervously look at everyone and apologize. Once, I saw him look around and find a box of Kleenex for a girl who was crying. I was proud like he'd scored a home run.
5. Shawna, a kid in Lorain County who I met when I was 19, but with any luck will be seeing again soon. Shawna has an aide who is always saying "I don't know what's wrong with Shawna today." But Shawna continues to come up to people and clamp her hands on their hands, and stare at their collars and shoes. She's a lover not a fighter, I mean love is her war.

16 July, 2011

I can't wait till I have a chance to synthesize my two email addresses so I don't have to go to as much effort to post here. I can never really dash off posts here, and just end up posting things on tumblr that are too long for tumblr and that I don't really edit the way I would if I was posting them here. Posting here has started to feel like a Big Deal where I have to write something well-organized.

This may be selfishness as a staff person, in fact it totally is, but I think the level of intense surveillance I'm required to keep up working at this camp is a little bit ridiculous. Someone I know recently got threatened with being fired because she forgot two of the campers she was supposed to bring to the pool--obviously forgetting to bring someone to an activity is bad, but I doubt she would have gotten in much trouble if she'd been with the campers and just lost track of time or forgot they were supposed to go somewhere. I think the really bad thing about what she did is supposed to be that she left them unsupervised, but they're two teenage girls with intellectual disabilities, not convicted felons. I'm sure their parents leave them home alone just as the parents of most teenagers do, but when they're here, suddenly we're supposed to be treating them like very young children.

And I mean very young--I volunteered in a mainstream first-grade class this spring, and I was surprised every time the teacher allowed a 6- or 7-year-old to go walk to the bathroom alone, because I'm so used to the idea that IF YOU'RE RESPONSIBLE FOR SOMEONE, YOU HAVE TO ESCORT THEM EVERYWHERE. Even adults with disabilities who live pretty independently and definitely walk to the bathroom by themselves when they're not at camp.

It kind of reminds me of the way Danny's teachers usually acted like there was something dangerous about special interests, but for his birthday they let him have a party totally focused on his special interest, and allowed him to talk to them about it. It was like they could hold two contradicting beliefs at once; there was a part of them that thought his special interests were cute and perfectly acceptable, but when they were doing their job, they thought the opposite. The rules about how to treat campers seem to contain a similar paradox, at least in their application. We know lots of them can do this stuff on their own. Most of us would say, if asked, that disabled people deserve to be treated "just like anyone else." But we don't treat them like anyone else at all, and if another counselor doesn't stand in the bathroom while their camper is taking a shower, we all cluck about it. We don't act like it's just a deviation from policy, but like it's actually dangerous.

I want to come back to camp next year because so many of the campers are really special to me and given location, taboo, and different writing/Internet abilities, we can't really be good friends outside of camp; but it's hard for me to imagine I will come back, because it's such a time-intensive job that I rarely get the chance to even read books or write posts or letters.

I keep daydreaming about trying to get a job at one of the two camps I enjoyed going to when I was a teenager. One of them is CTY, which is supposedly an academic camp for kids with high test scores, but is functionally a social space for kids who are different from their classmates. In my group of friends there, almost none of us had any friends at home. The other camp is a farm camp where the campers work on the farm and do group therapy together; when I went there, there were a fair amount of kids who had learning/developmental/psychiatric disabilities and had come to camp because someone decided it would be good for them, but there were also a lot of kids who had no disabilities and just enjoyed the environment. And, importantly I think, you didn't always know which was which. I've written some snarky things about this camp but I really admire what they do, ultimately.

I keep getting excited about the thought of applying to work at CTY or farm camp, not just because they're places I like, but because, oh my gosh, the freedom of being allowed to let campers go to the bathroom by themselves and only closely monitoring them if they actually need close monitoring and support! But then in the same breath I can't not just be staff, I can't help thinking how ridiculous it is that once you put people under a certain label all these new potential dangers emerge, like, THE DANGER OF WALKING BACK TO A CABIN ALONE, and, THE DANGER OF PUTTING YOUR HAND ON THE KNEE OF THE BOY YOU HAVE A CRUSH ON, that you must be protected from by your staff!

(On a totally different note, I've been meaning to link this since I read it, their parents are fantastic.)