I’m going to a community college in a city nearby, since I kinda… flunked out of the school I was in before. On the plus side, I REALLY like the classes I’ve been taking (3D modeling) and I think I may go for some sort of animation degree.

I’ve always wondered, though, if I should get accommodations. I mean, I am autistic, after all, and I do struggle in school to some extent or another, purely because I can’t fucking manage my time. But… What can the school do about that? I don’t even know what resources are available to me because I was denied any support when I was in the public school system (partly because the school system sucks, and partly because my mom’s reaction was basically “oh, well!”)

I know I could get a note taker. I’m sure I can prove that I have dysgraphia and that I never learned to take notes. But, here’s the thing. The reason I was able to manage in school before was… basically the reason my mom never really tried to get me help. Which is, the doctor said I was so smart that I’d make up for it. Which I have. I never developed the ability to take notes even when I had something to type with because, except in math class, I never really *needed* notes. The notes I take make absolutely no sense when I re-read them later because I almost always just remember shit. So I’m not sure I really need a note taker, and that would be embarrassing anyway.

But here’s the thing. Yes, I’ve made it this far using my intelligence to make up for my disabilities.

So how far could I go with proper supports?

But, what ARE proper supports? When I was younger, my mom would constantly ask me that question. “What can I do to help you do better in school?” But I never had the answer. How could I? If I knew how to do better, I would be doing better! Sure, it’s important to include your kid in discussions about their education, but it is in NO way the kid’s responsibility to know exactly what they need. The educational discussion should not start and end with staring at your kid, expecting her pull some magical solution out of her ass right then and there, and then saying “fine, but I can’t help you if you won’t help me!”

Blaming a kid for their disabilities is NOT an educational tool.

But it’s all I’ve ever really known.

So… What IS?


Wow, I haven’t updated this in like… 8 forevers.

Hm. Hi, if anyone’s reading this.

Uh, general update… No longer a teenager! Haha! I’m 21 now. Hooray for booze!

I’m almost thinking of starting a new blog… Revamping this one seems like….. Work. I dunno. The thing is, I like the URL, but some of the stuff this blog is about is kinda… Stuff I don’t really want to blog about anymore? I dunno. Words.

If anyone actually pays attention to the subtitle, you may notice that I removed the “transabled” part, and I’d just like to make it clear that it’s not because I’m no longer transabled. Because I am. But I’ve also realized that it doesn’t affect my life as much as it affects the lives of a lot of other transabled people, and I just sort of… Don’t want to talk about that, I guess. At least, not right now.

Also, I’ve realized that advertising being transabled seems to be a really good way to attract trolls, and I already do that enough on my tumblr and I’m trying to get away from doing it there, too. I’m debating about deleting the post(s) of mine that ended up on r/ tumblr in action (the spaces are there because I’m paranoid) because on one hand, I don’t want people laughing at me, but on the other, I don’t really want to bend to the whims of assholes on the internet and they haven’t really done anything lately. It’s really a delicate balance. I guess I’m boring (and that’s a very good thing!)

People-first Language and how its proponents silence those who are supposed to be “first”

I keep reading about people-first language (or whatever it is called) and… apparently I have an opinion about it, and whoa, I have a blog, so I guess I’ll talk about it or something.

For those of you who aren’t familiar with the concept, people-first language is an attempt to enforce “rules” about how to speak to/about a disabled person. For example, instead of saying “an autistic teenager”, one might say “a teenager with autism”. Instead of “a paraplegic” or “a paralyzed person”, one might say “a person with paraplegia/paralysis”. The idea is to put the person first (hence the name), implying that the person is more important than the disability, and that a person is not defined by their disability.

Now, I understand the idea. It’s a nice idea. But… Isn’t it more important to do that with actions, not words? Speaking in a certain way and trying to force others to do the same isn’t going to miraculously fix society. Somehow, I suspect that all this accomplishes is pissing people off. It sure has pissed me off.

Let me make one thing very clear before continuing. I have autism. Asperger’s syndrome, to be exact. Pretty soon it will all be the same thing though, so… I am high-functioning autistic (whatever that means). Most people don’t even notice it. They notice that I’m different, and often seem put off by my non-standard body language, but my behaviour doesn’t just scream “AUTISM” to most people. I usually don’t get stared at (as far as I know), I don’t generally have meltdowns in public, or make strange sounds (at least audibly). So I suppose that I just want to point out that I do NOT speak for the Autism community as a whole. I want to avoid flames down the road, if anyone reads this and pulls out the whole “well my brother has low-functioning autism and…” No. These are MY opinions, based on MY experience of the world as a person with the disabilities I happen to have.

I recently commented on a YouTube video titled “10 Things Every Child With Autism Wishes You Knew”. I’m sure you can find it yourself, if you like. The video, using amazing comic sans+MS paint+bad photography skills listed… 10 things every child with autism wishes you knew. Except, from the perspective of a mother of a likely LFA child. Not the perspective of an actual autistic person. How could they know what every child with autism wants? Does she know every child with autism? Is she omniscient? I’m not entirely sure. Anyway, the first “point” the video makes is as follows:

1. I am a child with autism.

I am not “autistic.” (picture of baby)

My autism is one aspect of my total character.

It does not define me as a person.

(next slide, black against dark blue, smeary with artifacts, nearly unreadable)

Are you a person with thoughts, feelings, and many talents,

or are you just fat (overweight), myopic (wear glasses), or klutzy (uncoordinated, not good at sports)?

Last I checked, a “child with autism” is an “autistic child”. They literally have the same definition. I refer to myself as autistic and see nothing wrong with it. Who is this woman to tell me that I don’t get to do that? I posted on the video, making the point that the video does not speak for all autistic people as it claims to, and that I do not agree with the content of the video and why. These are responses I received.

First, there was this gem…

the “child” should come before the “autism”…it is a point about indentity, and the importance of being seen as a person first, and, if necessary, identified as having a certain condition second…it may seem like a fine point to the average person, but to a person with autism, I am sure it is very important…that is my interpretation anyway…

I not-so-politely (I was irritated) informed the person that I was pretty sure that my opinion as an autistic person was more valid than their NT idea of what they are “sure” autistic people think. I was then informed of this:

….Sorry I was wrong…you are an asshole with autism….

And in one fell swoop, my opinion became invalid. It didn’t matter what I thought about people-first language and how it impacts people with autism, because I am an asshole. Assholes never have valid opinions.

Then, in response to a mother discussing the fact that her autistic son refers to himself as autistic:

Your son is male just as you are female. He is not just autistic. I agree with the video he is a male that has autism. What the video is saying is this – “Everyone is more than just one description, so your son is a male who is a wonderful person with autism. I have a 7-year-old grandson on the spectrum and he is so much more than one word. I hope you understand what I am trying to say. God Bless!

I’ll admit, this one brought about a rant with cussing. I told this ignorant woman that this guy can, in fact, call himself whatever he fucking wants and it’s really not her place to tell him he can’t. I ended the rant with instructions to get the fuck over herself. This was her response.

You are a very angry hurting person for sure. I never said my opinion was more valid. I was simply trying to explain what the video was saying about a person with autism. I am praying for you.

EXCUSE ME? Because I disagree with you, I am “angry” and “hurting”? That’s ANOTHER excuse not to listen to my opinions! “Oh, she’s angry and hurting, it can’t have anything to do with the way I treat autistic people though! She’s just lashing out because other people don’t understand autism. How sad. I’d better continue to ‘educate’ people about what people with autism want. I’m such a great neurotypical for standing up for these people who have no voice!” Meanwhile, I’m screaming “NO! I’m trying to tell you what I want, why won’t you listen!”

Don’t people realize what they’re doing? They pretend to care about what autistic people think, but then when an actual autistic person tries to participate, they are labelled “asshole”, “angry”, “hurting”, “selfish”, “hates parents”, and other hurtful things, so they don’t have to listen to our ideas and opinions.

It just makes me SICK.

(I should point out that the parts I wrote, that aren’t italicized as quotes, are based on a combinations of a lot of attitudes I have encountered, while the parts that ARE indented as quotes are copied and pasted from the comments page. Just to avoid any misunderstandings.)

I suppose what I’m trying to say is… I do not have anything against the concept of person-first language and I understand what its proponents are trying to do. What I have a problem with is how they try to force it on EVERYONE, saying “this is what autistic people want” because I am autistic, and I honestly don’t want that. I honestly couldn’t care less about that, there are much bigger issues to be addressed. Even if I am the only autistic person who does not care about people-first language (which I know I’m not) the generalization of “this is what all autistic people want” is inaccurate. Just like any other broad generalization like that. I suppose it’s like being a white person, standing up and saying “all people of African descent with dark skin want to be called (black/african american/whatever term)!” Because, no. For one, my fictional person is not black. How do they know what all black people want, if they have never been black? I’m not black and I don’t claim to know what all black people want. In fact, someone may take issue with my calling people ‘black’. And that’s fine. I’m not going to pretend to know what the best term is. Two, regardless of what term the person uses, I can virtually guarantee that if I looked hard enough, I could find a black person who doesn’t care if they are called that or not. Because black people are STILL INDIVIDUAL PEOPLE, not some sort of “hive mind” with all the same opinions. Saying anything about “all black people” or “all autistic people” or any other generalization is going to be untrue about SOMEONE.

Unfortunately, within the autism community, the people making the generalizations are often the people in power. If an autistic person speaks up, and voices their disagreement, they are immediately classified as “not really autistic”, “bitter”, “parent-hater”, or many other things to silence their opinion.

Ok, I give up on that for now

Yeah, I know, I said I would have a super-fancy-tastic post up here, but… I lied. I’ve been too busy to actually organize my thoughts. Maybe I’ll write it later, just not right now.

I am gonna try to update more though, because I really want to have a good blog! =P

Not much has happened since I last updated. Well a lot has happened, not much has really changed. Except that I have a math test to study for. I guess I better get on that…

Bye for now!

Update of randomness

I’ve been busy lately, but I’m in the process of writing a much more awesome post… but until then you’ll just have to make do with this random update. I’m trying to get caught up in school at the moment (stupid mono) and being yelled at by my mom at every opportunity. For example: I left my bedroom door open yesterday when she was screaming at me to hurry up and get out the door (we were going to the dentist to talk about my wisdom teeth, which were supposedly impacted and never going to come in, but then they… did… without causing ANY problems. GOOD JOB DENTIST. anyway..) and so while we were there, the dog went into my room and ripped up a kleenex all over the floor, which I got to clean up. Then later, she got sick and threw up. Then, my mom asked me over and over if there was anything the dog might have gotten into while she was in my room, and pretty much accused me of being on drugs about ten times in the process. I think her basis for this is my insistence on taking my Adderall when I need to actually get things done, rather than just relying on the fact that she “believes in me”.

But, that is somewhat the basis of my next, more awesome post, so I won’t go too much into that.


Mono and Christmas (general update)

I had about half a post written about how I had mono and was really tired, but I was too tired to finish it. Now I’m feeling a lot better and decided to just rewrite it.

Apparently around Thanksgiving, I caught mono. I don’t know how or where I caught it, but I did.

When I was at the doctor’s though, we discussed other things like me seeing a shrink in the future, and I mentioned that I thought I had Asperger’s. She laughed, explained that she had 2 autistic children at home, and told me she was going to ask me if anyone had ever mentioned that before. Having an actual medical professional agree with me on that was really awesome…

In other news, I got some awesome stuff for Christmas! 1 Settlers of Catan extension, 2 Settlers of Catan expansions, some slippers, a robe, some money, a silly card game, an awesome dragon incense burner, knitting lessons, and some other stuff. W00t!

I’m a thief!

This is stolen from a post on WrongPlanet… I just liked it a lot. The writer is Christian, though, so the ending is kind of… Wut… But the rest is good. For those of you not familiar with WrongPlanet, it’s about living with autism. Basically, it tries to make parallels between some fictional mind-readers and neurotypicals, and an explorer and an aspie.

A man was exploring an uncharted region of the world and encountered an isolated community of people who could read each others minds. They had the capability of opening up their thoughts for transmission to each other, and likewise they could close their thoughts at will but doing this was considered very rude among them. This mind reading was accepted as normal among the community, and they had developed their own social rules for its use. Fascinated, the man decided to take up camp among the apparently friendly and accepting community of mind readers for a time to get to know them better.

When the explorer met these people, of course he could not read their minds, and they could not read his. They viewed this as a deliberate act of the explorer closing of his own mind to them. They thought, what a peculiar fellow. He should be willing to open up his mind like the rest of us do. They brought this to his attention as an admonishment, and when the explorer explained that he was unable to read their minds, they did not quite believe him because after all, everybody can read minds. They said he was being stubborn and self centered closing his mind off like that. They let him know how rude he was behaving, and that he needed to be more considerate of others. The man was confused with the strange social dynamics of the community. More than half of their interpersonal communication was done through mind reading. Everyone knew what each other was thinking, and seemed to respond easily to one another. But when the explorer tried to interact with them, he was given responses of frustration because he did not pick up on what the other people were thinking. This offended the mind readers, and they started to rebuke the man for he was being rude and inconsiderate toward others, not even taking their clearly projected thoughts into account like any truly caring person would.

Constant accusations of only “living in his own world” became frustrating and nobody understood or even believed that he was simply unable to read their minds. The explorer felt frustrated and alone. He did not wish to offend others, but it seemed to happen so often he decided that it was easier to spend time alone where he would not be viewed as rude and inconsiderate. The man spent many hours alone in his hut crying and praying to the Lord to give him the gift of reading minds so he would be accepted by the others. In his heart, he felt the Lord saying, “My grace is sufficient for you. Remember, the world did not accept Me either.” This helped some, but he never was able to form close relationships with the mind readers.


I… I’m going to have a stepdad and a stepbrother. It’s official.

I’m not sure what to think of that… I mean, I knew it was coming, but just not so… right now! So! That’s… Uh… Wow.

I finally got SecondLife working, by the way. I got a wheelchair for my avatar! I really hope I can find people there who don’t hate me for who I am… Sometimes they’re hard to come by, you know. One time, I told someone on IRC what was bothering me and why “finding Jesus” or whatever he was saying wouldn’t help, and he called me creepy… That make me really sad.

I wish I could just be myself, without being afraid. But there are so many hateful people in the world who wouldn’t understand that I didn’t choose this. Sometimes I wish I wasn’t transabled, but often I realize that if I wasn’t transabled, I don’t think I’d really be me.

I’m stating the semi-obvious now… I’d better go to bed before I start stating the very very obvious — oh look, the walls are beige. There’s a dent in the wall. (Oh no, I’m already too late!)

Maybe I’ll think of a real post tomorrow, at a decent time so I’m not completely exhausted…

Analysis of my current mood

I’ve been ordered to try again on the whole “writing” thing. So, here goes.

I have a paper to write. It is very late, but the teacher says she will accept it. My mom is bugging me to write it, making me less likely to actually do so. I really WANT to write it, but the more my mom nags me the less inspiration I have.  But if I tell her that, she’ll yell at me. So I’m stuck.

Thanksgiving was… Okay. I saw a lot of my cousins, but it wasn’t as fun as past years. My cousin who I shall refer to as Ginger (due to her hair colour) used to be the reason I loved Thanksgiving. It was the only time of year I got to see her. She’s 2 or 3 years younger than I am, putting us close in emotional age (I have been pretty consistently 2 years behind in most things, from my own observations) and so we got along great. We used to play with little Rudolph the Red-Nosed Reindeer toys, and watch movies, and every year we made a turkey out of vegetables with help from our other cousins, and we would play on the computer. We had a Millsbury account we shared (we were really cool) and when we were REALLY young (before either of us was anywhere close to puberty) we’d take a bath together. Well, over the past few years we started growing apart. When I hit puberty I didn’t change much. We were still friends. When SHE hit puberty, she changed COMPLETELY. She’s a cheerleader and wears tight trendy clothes and acts like an idiot because she thinks it’s “cute”. She has completely rejected me and my nerdy ways. We didn’t say a word to each other this year (although I tried, I asked if she wanted to play a game and she didn’t even respond). So, that was depressing.

Something that has changed recently is now my mom brings her boyfriend to Thanksgiving. He sometimes brings his son. I think I need to come up with a nickname for the son besides Stepbrother, but that will have to do for now. So, I hung out a lot with Stepbrother this year, and we played Settlers of Catan and he played his guitar. He’s cool. But I’m getting tired of spending time with people. I need time alone to recharge if I am to be at all social or productive. I was not given a single opportunity to do so all day, then my mom couldn’t understand why I was so antisocial and unproductive.

Another thing is that my back hurt a lot today. I need to stretch out to make my back comfortable, and I try to when I need it. But today when I was sitting in a comfy chair, I put my feet on the footstool so I could stretch and immediately mom’s boyfriend decided he needed the footstool and moved my feet so he could sit on it. I couldn’t lie on the floor because I’d be in the way. So I just dealt with it.

Now I am at mom’s boyfriend’s house, 3 hours from home. He lives 3 hours from my grandparents’ house. I don’t want to be here. I want to go home.

I feel like I’m going to cry.


I have been informed that I have to write something.

I don’t want to write.

I want to play SecondLife.

But I can’t, because they won’t let me onto the adult grid! I’m stuck in the teen grid, which is BORING.


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