Showing posts with label ableism. Show all posts
Showing posts with label ableism. Show all posts

Sunday, February 23, 2020

Reflection: Neurodivergent Teacher Trauma

I know I’m a good teacher. I know I don’t have to control everything. Yet, I always feel a need to prove myself. I see every disagreement as a challenge to my knowledge and skill. (And that fear, which is what it is, is exacerbated when I know I have current research on my side.) I know full well that, to my frustration, I do not have the social skill to make people see my way of interpreting the evidence. Trauma and fear means I often give in to avoid the situation when the other person presents a reasoned argument. For years, I have marveled at the people who are able to say exactly the same thing I just said and get people to agree with them. It’s a skill I don’t have. Body language? Tone of voice? Social rapport building? Probably a combination. Whatever it is; I don’t know how to do it. That’s a problem when you have a social communication disability and you’re being evaluated on your ability to coordinate a cohesive team unit. The problem is even worse when not everyone is coming from the same background/approach. (And the problem is only exacerbated by the experience of administrators who invalidated my voice in the process, or who flat out told me they didn’t believe I could do it. I haven’t learned better strategies, only more fear.)

I feel safest in a very silo-ed approach. I feel most comfortable if there is allowance for disagreement in approach among team members, but we all can do what we believe is best. I believe students benefit from multiple approaches, and that’s part of it. The other part is that because I don’t feel threatened, I’m able to work more cooperatively/productively with everyone on the team. But that model is not acceptable in modern special education. Consistency is the name of the game. We all must be on the same page, defined as taking the same approach to everything: lock stock and barrel. That makes me very uncomfortable. I’m neurodivergent; I simply don’t think the same way as everyone else. 

I tried working in an ultra-“consistency-is-everything” environment back at the beginning of my career. That experience marks clearly the start my education-system related trauma. Back then I totally drank the kool-aid. I believed in the system completely. Unfortunately, that school quickly and explicitly showed me that my brain didn’t respond to stimulus the same way. Purely by virtue of being neurodivergent, I was physically unable to live up to their standard of consistency. That experience has colored my feelings and approach to the whole concept ever since. (I’m not sure I was explicitly aware of it until I just typed that sentence. I knew the trauma was effecting me emotionally, but I’m not sure I understood how it was effecting my work until now.)


I’ve known for several years know that my trauma and my neurodivergence were causing most of my stress at work. I knew I was part of the problem (everyone has a role in a social interaction problem.) I knew my trauma stemmed from the reactions I’ve received over the years to my neurodivergence, but I always focused on the ableism in special education as the root cause. Special Education is incredibly ableist, but in reality I’m quite good at navigating that aspect of my chosen field. This trauma is pedagological. That’s why I have never been able to figure out how I could be successfully accommodated. I still don’t have an answer for how that can work in the future, but now at least I’ve started asking the right question.

Sunday, December 1, 2019

A Part Time AAC Using Teacher in an AAC Classroom

I’ve been using AAC a lot at home recently. It feels really good. It feels comfortable in a way that mouth words don’t. Mouth words are stressful even in non-stressful situations. They tend to tumble out of me unbidden and uncontrolled. Ensuring that the correct words come out in the correct order with the correct tone at the correct time.... I can usually manage most of that, but rarely all of it, and it’s a lot of work. And don’t ask me what I said. I rarely have a clue.

Still, although I often text across the classroom or across the building for communication access, I’ve never seen AAC as a viable communication tool in the classroom. What’s frustrating is that it’s not for any practical reason.

It’s feeling like I owe people explanations I don’t want to give for why I’m doing things differently than I used to. I don’t owe anybody any explanation I don’t want to give. “I can communicate clearer this way” is enough. I say that. I’m not sure I believe it.

It’s feeling like I’m sending mixed messages or like I’m not providing a good model for my students and staff of the expectations for language modeling or AAC device use because even when I’m using AAC, I tend to mix it with mouth words. I’m a part time AAC user and that’s hard to explain. (It’s also different from my students who are primary AAC users or my students who use AAC for communication repair.) I understand the difference. I’m still afraid others won’t.

I know the answer, like all the accessibility tools I’ve tried incorporating into my classroom routines this year, is “try it and see how it works for you.” I don’t know why this one feels so different from using mobility aids. Maybe it’s because we teach students to use AAC and we don’t teach students to use canes? Really, that should be all the more reason to do it.

Maybe I’ll try on Monday. Assuming we don’t get snowed out.


Monday, July 15, 2019

Queer Eye: A Problematic Relationship With Disability from the Start

There’s a new episode in the upcoming season of Queer Eye that’s getting, well deserved, derision from the disability community for the title “Disabled But Not Really.” The primary frustration I’ve heard is that Queer Eye has steadfastly ignored the Disability community for so many seasons and episodes, and then chose this, extremely problematic, individual to highlight as their one “disabled makeover.”

My argument is simple. Queer Eye hasn’t been ignoring the disability community. They’ve had a problematic relationship with disability throughout the run of the show. 

Many of the individuals they have made over have explicitly said during the episode that they currently have or previously had a diagnosis of depression. Depression is a real mental illness. It is a disability. But the way Queer Eye treats it, giving them a fresh start is the cure. (It’s not.) There’s a reason that the dramatic “after the makeover” parties that end the episode are videos of the day after the intervention, and not a week or month or year later. That kind of intervention is exciting and fresh, but doesn’t have long term effects. I’d love to see them do a “Queer Eye: One Year Later” special and prove me wrong, but without follow-up intervention, the research is on my side.

The other problem the show has with it’s approach to disability is Karamo and his entire approach to the makeover project. He’s a charismatic guy and it’s easy to see why people connect with him. But his fundamental problem is he’s a one trick pony. To look at him, it’s obvious he takes fitness seriously. So it’s no surprise that he uses physical activity to “get people out of their comfort zone” in almost every episode. I recognize that we need that “made for TV emotional moment” for viewership. But the show misses the opportunity, every single time, to acknowledge that the “aha” moment is just the beginning of a much longer process, and that process won’t happen automatically. Every time, the show misses a real opportunity to reduce stigma and provide awareness about mental health resources that could provide long term benefits not just for the individual on the episode but for all people living with mental illness.


Queer Eye has made a start in trying to be more inclusive. They have simply fallen prey to what most of media falls prey to. Lack of representation or consultation within the production team. They don’t know what they don’t know. Much like Karamo only really knows how to get people out of their comfort zone and get that emotional moment using physical tools to get that “aha” moment, the show only knows how to portray a snapshot/momentary intervention. I encourage the show to reach out and partner with groups like NAMI to provide resources and connections that have the power to truly change people’s lives. Queer Eye has the voice. They say their goal is to promote inclusion and acceptance. My hope is that they learn from the feedback they have gotten from the disability community, step up, and use that voice to promote the resources that will create inclusion and acceptance for ALL.

Sunday, June 2, 2019

Sexuality in the Special Education Classroom

CN: “sex ed” 

There is no room for sexuality in the special education classroom. It’s a difficult and controversial topic in general education that gets largely ignored in special education. Students with disabilities are either viewed as non-sexual (eternal children) or hyper-sexual (sexual deviants). Those who fall into the first category don’t get sex ed at all. The second group do get sex ed, but it’s “sex ed for special education.” Sex Ed for Special Education covers: public and private - what you can do where, circles of friendship - appropriate behaviors around people you know more/less well (aka not everyone is your best friend), and hygiene.

If you’re wondering where the actual “sex ed” is in that curriculum, that’s pretty much my point. Hygiene is as close as they come to “why my body is changing” and I’ve seen some pretty fascinating misconceptions about how the adult body works from my adult students as a result. But I only knew about it because I was supporting them in the residence in the evening when they were confused and overwhelmed and unable to express it. Most teachers don’t get that opportunity to interact with their students in that setting and most residential staff don’t have the time or training to provide the feedback to the educational staff. (And that’s assuming either side is willing to listen or do anything about it.)

Somebody did ask, at a recent conference I attended on teaching sexuality to students with significant needs, about teaching about sexuality, safe sex, or dating. The presenter dismissed this as a non-issue for this population, stating “if a student expressed an interest in any of these areas we would address it on a 1:1 basis, but it hasn’t come up.” Of course it hasn’t come up. Most of our students don’t know how to ask. It certainly isn’t default vocabulary in anyone’s communication device. Typical students have extreme difficulty talking about it and finding someone who they trust enough to talk to. We are expecting students for whom basic communication can still be a challenge, and who may only have a few people in their lives with whom fluent communication is even possible, to initiate these conversations?


But that won’t change. Because that’s not the point of Sex Ed for Special Education. The goal, like the goal of most special education curriculum, is to get those uncomfortable box 2 students back into box 1 where they make their typical educators feel more comfortable. Without changing that paradigm, sexuality will never be allowed to exist in the special education classroom.

Wednesday, April 3, 2019

Teaching While Autistic

To the outside world, I’ve had an incredibly successful 10 year career as a special education teacher. (You could argue 20 year career, if you count the time I spent working in residential services before getting my teaching certificate.) But under the surface lies a deeper struggle. A struggle not just with trying to reconcile my professional identity as a special education teacher with my personal identity as an autistic person, but to try to figure out how to survive as an autistic person in the incredibly ableist educational environment.

Part of my problem was, because I wasn’t diagnosed until I was 30, I had no experience requesting accommodations. And since most people still think “wheelchair” or maybe “blind person” when they hear “accommodations” my supervisors had no idea what to do either. (Even at schools for students with autism! Especially at schools for students with autism!)

And so my journey progressed from “how are you going to help yourself” to “We’ll help you” without any clear understanding on anybody’s part (mine included) as to what that “help” was going to look like, or exactly what I needed “help” with.

Should we be surprised that those positions didn’t work out?

So before I try again, it’s obvious there’s something I need to make clear to myself and to my prospective employers. I need to know, in concrete definable terms, exactly what I need from them in order to be successful in the position they are hiring me for. And if we cannot define clear, concrete supports that will make the position successful, either because what I would need to be successful is too abstract or because we are unclear on what would be required, then the position is not a good match for me and I shouldn’t apply.


I’m tired of hiding and trying to pretend there isn’t an issue here. I’m tired of supports that are really just attempts to recognize and fix things after the fact. I love what I do, and I’m not going to give up on my career. But it’s time to find a place where I can do it without pretending to be someone I’m not.

Friday, February 22, 2019

Coping Strategies

One of my personal projects recently has developing a system to track and analyze my energy regulation. I’ve been trying to figure out if I can predict and even out the highs and lows I’ve been having lately with more better self accommodation. The jury’s out on whether I’ve made any significant breakthrough (and that’s a different post) but as always it brought me back to the question of instruction.

I wrote about my emotion-based instructional curriculum a couple of years ago and what I’ve been doing hasn’t changed significantly in the intervening time. But thinking about it from this perspective, there’s an obvious piece missing. There’s an obvious ableism embedded in that curriculum that I didn’t even notice. Nothing there teaches students to recognize the coping strategies *that they are already using.* Nothing there teaches them to understand how they might need to modify their current coping strategies to function more effectively in a neurotypical society. (Which, like it or not, is the one we live in.) It assumed that the student didn’t have any coping strategy (not very likely for my older teen students!) and tried to teach them the ones that neurotypicals thought were a good idea. Yet we know that the  best teaching is building on skills *that are already there* not trying to build new skills without a foundation.


It seems so obvious when I say it like that, doesn’t it? Time to put it into practice!

Sunday, November 4, 2018

When We Were Alone: Teaching our (Current) History with Residential Schools

The picture book study for this year’s Global Read Aloud was a pair of indigenous authors and illustrators. The use of language in the books was rich, and gave us ample opportunities to make connections to our own use of multiple communication strategies, as all of my students this year are multimodal AAC communicators. The themes fit beautifully into our social-emotional instruction, as we have been focusing on working together and what it means to be a community.

Then we reached the last book in the book study, “When We Were Alone” by Richard Anderson, illustrated by Julie Flett. The book makes great use of repetitive language that helps make the complex topic of indigenous residential schools more cognitively accessible. I have a student in my classroom who was previously placed at a residential school “far away from home” (as the story says) and who has a trauma history from that placement. I was initially a little apprehensive about reading this story with him. Would he understand it? Would he make the connection? From the first read-through, this student, who usually has difficulty sitting for lessons, sat with rapt attention for this story. His eyes were glued to every page as I read. It was clear the story had his interest. 

I did not draw, or ask him to draw, explicit connections to his own residential school experience. What we did was make explicit comparisons between the meaning behind the rules in the story “to make everyone the same” and the rules in our classroom “to be safe” “to get our work done” and “so everyone can participate.” My students’ active participation in these activities reinforced our classroom values more than any explicit teaching could have done.


I will say it explicitly here: My student’s former placement was a residential ABA program. While the stories are different, at far too many programs the strategies and intentions are the same as the story we read. ABA-based strategies, applied to appropriate skills, are not, by themselves, the problem. It’s the values and intentions that drive them that are deeply problematic and lead to student trauma. For teachers looking to broach this controversial topic with their class, this book may be a great place to start.

Tuesday, July 3, 2018

The Mask in My Teacher Toolkit

I try very hard to create a classroom that is welcoming of students natural ways of moving, of interacting with the world, and of expressing themselves. In the adult autistic community, we talk a lot about masking, and the effects of it on self-esteem. And then I watch my neurotypical colleagues, completely unaware of what they’re doing, expect those masking behaviors. And I watch myself use them all the time as well. And in makes me wonder, am I doing a disservice to my students by not teaching those skills?

Masking is a skill. The more skills you have, the more opportunities are available to you. But what if our students grew up knowing, not just that masking exists, but that it is a choice? The social skills curriculums currently out there teach “this is what you have to do” but how different would the educational experience of the next generation of autistic children be if we taught it as “this is what the NT population does/expects.” What if our behavior expectations where “here is how to do it/fake it” and “here are reasons/times when you might want to.” 


I know full well that my ability to pass, and thus have control over disclosure, has given me opportunities I might not otherwise have gotten. (There’s a reason this blog is anonymous.) My students may never pass for NT due to other disabilities, but don’t I owe it to them to give them the skills to try if they want to? When I have struggled with social interactions, I’ve gotten instruction (I, personally, found Michelle Garcia Winner’s Social Thinking at Work and Ian Ford’s Field Guide to Earthings particularly useful.) Why shouldn’t they benefit from the same opportunities? As a special educator, isn’t that my job? To make the general education curriculum accessible to my students?

Sunday, April 1, 2018

Emotions in the Autism Classroom

I teach a social skills curriculum with a focus on recognizing and labeling emotions in self and others. We do a lot of work in that class around matching emotions to their associated behaviors, both the classic NT expressions, and students personal expressions of those emotions. 

A number of years ago, I was teaching in a very bad situation involving bulling and emotional abuse. I was too naive and oblivious at the time to be aware of much of what was happening until the situation got really bad, which is a familiar refrain for anyone who is or loves someone with significant social communication challenges. I thought I was handling it. I thought I had someone in my classroom I could trust. I was very wrong on both counts.

The instructional data from the class I was teaching at the time was very clear: the students could match feelings to behaviors given pictures, but when using video, or during role-play, they were unable to even identify how someone was feeling. Even when the actions were labeled for them (the same actions as the pictures they had memorized) they were unable to connect it to the feelings.

Yet, toward the end of my experience there, when things got really bad, my students made it very clear that they were very aware (more aware than I, myself, was) of the emotional situation in the room. One student, every time both staff were in the room, came up to me asking “Sad? Cry?” Long before I knew what was going on, another student, who had no history of aggression, began attacking the staff member who was the primary source of the abuse.


The instructional data is clear, these students did not understand emotions and their connections to behavior. But the evidence of what they did proves the data to be wrong, or at least incomplete. They couldn’t show their understanding in an academic or assessment context, but they did one better. They demonstrated them in real-world context with the people that mattered to them and had influence over their lives. Isn’t that the whole point of teaching the academic skills in the first place?

Friday, March 30, 2018

Gender in the Autism Classroom

I teach middle school, so it’s probably unsurprising that I have had many students over the years who “like young pretty girls” and show it through their behavior. While I’m no longer a young teacher, and I’ve never dressed particularly effeminate, I’ve always looked younger than I am. And none of those students have ever had those issues with me. In general, I’ve always been able to work with the students who have sexual issues around females. Partly, this is because the behavior just doesn’t bother me, but partly its because they don’t generally exhibit those behaviors toward me. For whatever reason, I don’t trigger “pretty girl” to them.

You see, I present as female. A short, rather busty, female at that. I use she/her pronouns because they match my physical presentation and are really the only ones that make sense to me. But I’m agender. The whole concept of gender and gender distinctions really makes no sense to me. And, it seems, my students can tell.

One of my students this year is constantly labeling people (especially girls.) And for the first part of the year he kept asking me “girl?” (He wasn’t doing this to any of his other teachers.) And I kept saying “yes” because well, it seemed the simplest answer. But he kept asking. Finally, I changed my answer to “sometimes, on alternate Tuesdays when there is a blue moon.” And he hasn’t asked me since. He knew. I think all my kids have known. It’s why I’ve always been their exception to the gender rules around their sexual behavior. Because, somehow, they can tell my gender doesn’t follow those rules.


It’s just another of those things parents/teachers/professionals tend to assume our students “aren’t aware of.” My experience says they’re usually more aware than anyone else around.

Saturday, February 17, 2018

(Neuro)Divergent: The Classroom

It’s funny, I used to be called “the mean teacher” because I would insist on students doing everything they could independently, no matter how long it took, and not letting others “save” them. Because I insisted on teaching grade-level content to all my students, no matter their academic skill access level.

Now, I’ve changed schools. To the school that was closest aligned to my values that I could find in the state. And all of the sudden, I’ve developed a reputation as that teacher that is too permissive. You know the one, the one that lets her kids get away with everything and doesn’t actually teach? Yeah, that’s how I’m being perceived.

So what happened?

I could point to any number of things. I do have a really hard class this year. Certainly harder than I’ve had in a while. Groups don’t look very group-ish most of the time. And certainly, I’ve had more lessons fail than I had gotten used to. That’s only a problem when I’m okay with it and don’t learn from it. (And it’s the cause of my discomfort, not the school community perception.)

No, this reputation came about because I have found the hard edge of their tolerance for neurodiverisity. I knew it had to be there: schools are staffed by neurotypicals and even the respectful ones are limited by their perceptions of the world if they’re not listening to the voices of the neurodivergent community. And I noticed that from day one when I started at this school. It was far more respectful and understanding of the neurodivergent community than any place I had been before. But it was still an “us” and a “them” and the voices of the neurodivergent community were conspicuously missing from the conversation. (I left feedback saying as much on my evaluation. I doubt it made a difference.)

That’s what the perceived “permissiveness” is: I’m being too neurodiversity friendly. And, as often happens, it’s being perceived through neurotypical eyes as letting them get away with too much: because it makes them uncomfortable, because if they were me they would not let him do it. And so the “he needs to learn he can’t do that out in a job setting” argument gets invoked.

I literally got told that I’m really good at keeping kids calm and preventing them from getting upset so they can learn. And that that is a bad thing. Because they need to learn to handle being more uncomfortable. (Them being comfortable is making the staff around them uncomfortable.) We need to sacrifice their learning so they can accept more “appropriate boundaries.”

And to some degree, of course, they’re right. Because outside my neurodivergent-friendly classroom, the cold neurotypical world won’t accept them for who they are. And they will be forced to accept arbitrary social rules in the name of “appropriate boundaries” in order to be successful. And we all want them to be successful.

So, where do we go from here?

  • We use a more typical token or points system on are goal-directed-learning project. (Honestly, that was probably the next step in understanding how to reach our goal anyway. We needed to make it more concrete.)*

  • We set up clearer physical boundaries in the classroom. (I’ve already bought painters tape. Wish I could remember the name of the teacher I met on Twitter who gave me the idea a couple years ago! Thank you, Awesome Autism Teacher Who’s Name I Forget!)

  • I have some social skills curriculum to write. And some social stories. They need to come from me because they need to come from a neurodivergent perspective. (Unless someone else out there has already written one? I don’t need to reinvent the wheel!)

I’ve got my work cut out for me changing the perception of myself at my students at my new school. But I think it’s worth it. Because this school really does have the right idea and the right values. It’s why I chose to work there. 

Even when we have neurodiversity acceptance in our society I don’t think we’ll ever have neurodivergent-friendly classrooms the way we have neurotypical-friendly classrooms now. And that is what I was trying to create. And honestly, if I believe in inclusion, which I say I do, that shouldn’t be what I want. Our goal should be a neurodiveristy-friendly room. One that works for all of us, neurotypical and neurodivergent. They are right, I went too far to one side. It’s time to re-build the classroom that works for all of us, because that’s the classroom that is really going to prepare students for “the working world” after graduation.


*I know the research on reinforcers. I’ve read Punished by Rewards. I’ve read Mindset. But I work in a PBIS school that wants to increase its use of PBIS. That means using rewards. I have some ideas about how to make this work following the TTOG principles. I’d been trying it before everything fell apart in the last month or two and having some really awesome successes, even in the DTT context, that I hope to get to write up at some point.

Sunday, December 3, 2017

The Gift of Flexibility

The rules that make up our social structure can seem arbitrary when participation is not intuitive: Go here now but not later. Touch this but not that. Put this here but not there. When you look for an underlying logic in order to understand them, as many autistic children and adults do, it appears they change on a whim. “Go with the flow” requires recognizing and understanding, or at least being able to follow, the “flow” of society, which is based on social norms - the very skill that eludes so many people on the spectrum. It’s really no wonder so many cling to routine, structure, and sameness and get upset when it is violated. From that perspective, it’s actually surprising more folks on the spectrum don’t spend more time in “fight or flight” mode. It is a constant battle to figure out how to live in a world that often doesn't make very much sense.

Engaging with the norms and expectations of the school and classroom environment is particularly challenging for several of my students. In particular, they do not recognize the logic behind sitting and completing an academic task, moving to another area, and repeating the demand. Both sitting and moving are non-intuitive demands. Both have, historically, had intensive intervention aimed at compliance with these demands. 

They often demonstrate their lack of understanding by removing themselves from the demand to engage in preferred activities which are both highly interesting to the student and engage the teacher in an interaction, thereby drawing both of them away from the interaction they do not understand the logic behind. What concerned me was students who were getting bigger and older (I teach middle school) and more aggressive. And we were the cause. (Of the aggression, teenage boys are going to grow like weeds whether we want them to or not.)

I met with the team and we got programs put in place to get everyone’s hands off the students unless there was a real immediate safety risk (e.g. about to be hit by a car!)

We got lots of alternative seating in place. More than enough for every student in the room. Ball chairs. Bouncy chairs. Rocking chairs. We stopped telling students to sit and started asking them where they wanted to sit.

We got some pretty ridiculous answers at first. On the table? On the heater? On the floor?

We said okay. We did our academic work there.

Sometimes students didn’t want to sit. They stood or leaned.

We said okay. We did our academic work there too.

It wasn’t perfect. Kids were still on the move a lot. Transitions were not flawless. But what changed almost immediately? The day we made this change, the aggression that was starting to become a problem disappeared overnight. We’re getting just as much work done as we did when we were following the compliance-based program with one difference: everyone, kids and staff, are happier. We’ve been at this for a couple of weeks now and an unexpected thing has happened: the kids are starting to sit. They are sitting in chairs and without being asked. The logic is simple really:


Stop fighting the kids and they’ll stop fighting you. It’s the gift of flexibility.

Sunday, November 12, 2017

Starting to Explore Together

It’s way too easy to fall into a rut of un-reflective discrete trial training (DTT) use. The data is hard to argue with: students work their way methodically to mastery of each item, and when you’re talking about basic identification skills they do master item after item. For many students, they fall into the same rut. It’s comfortably predictable: “I point to this, I get what I want.” Is it any wonder that so many students (and their teachers) have trouble “going beyond” DTT practices? It’s a monster of their own creation.

And so, the question remains: how can we give students that predictable instructional environment without feeding that monster? How can we encourage them to grow as learners while supporting their need for security and sameness in a world that, often, doesn’t make any sense to them? 

The first answer is easy: let students stim. That’s a no-brainer. But the second isn’t that far behind: Build on the objects and properties that interest the student. Our students tend to notice and focus on properties no one else is paying attention to. It’s one of their strengths and it’s one of the reasons neurotypical teachers find them hard to reach. They’re busy focusing on how the object tastes or if it flies when the teacher wants them to count! Let students get to know all the properties of the objects you’re working on. (Yes, explore the textures, tastes, how far they fly, if they bounce, etc.) It might take longer to learn to count, but if you step into the learning, use your language learning strategies (e.g. aided language modeling), the student will actually come out ahead on the other side. More importantly, they will come out with their sense of self intact and validated. They will be ready to take on bigger and more complex learning challenges because they have the foundational skills and because they have the belief in themselves as learners. Even the best intended teacher-driven task memorization cannot accomplish that.

Saturday, September 9, 2017

What Is Behavior?

The operational definition for an educational context that I’ve always heard for “behavior” is: something you can observe the student doing.
When I googled the definition I got “The way in which one acts or conducts oneself, especially toward others” or “The way in which an animal or person acts in response to a particular situation or stimulus.”

Almost anything a student does is observable. It is the social context, as put forth in the first definition, that determines whether it is a behavior (conducting oneself in relation toward others.) 

To put that in a behavior tracking context: We can observe anyone breathing, but for most students there is no reason to track that as a behavior. For a student who is severely respiratory compromised, for whom continued ability to maintain consciousness (and therefore maintain any relationship with others) is a concern, it is a very appropriate behavior to track.

The problem comes, I think, not when we try to define the behavior (defining observable behavior is a skill, but is one that can be mastered with practice.) Where we struggle is in defining the social context. When the norm is typically developing age-peers, almost everything a student with high support needs does will be considered a behavior, because the things they do successfully and independently often look very different from their peers: indistinguishability does not allow for the beauty of neurodiversity. However, when the norm is peers with high support needs, we are often setting ourselves on a slippery slope of low expectations: “this is the best they can hope for so we just have to accept it.”

The justification I so often see for tracking indistinguishability behaviors (stimming, eye contact, etc) is that that kind of behavior will not be accepted “in the real world.” There are certainly neurodiverse individuals out there spending a lot of energy practicing indistinguishability behaviors in order to be successful “in the real world” right now. What would it take so they, and our students, didn’t have to?


In the classroom, we have near-complete control over the social context. And the social context that students learn in school is the one they will bring with them into the adult community and workplace. If we build a classroom community that values neurodiversity over indistinguishability, that is the social context that students will learn. It has worked for successful businesses like Google and Apple. It will work in our classrooms too. And it just might change the world for the better.

Monday, May 25, 2015

Presume Competence

Since I work with students best described as "consistently inconsistent" I frequently find myself going around and around with well meaning colleagues on the idea that students need to "prove" that they know A or B (usually vocabulary.) (As if any typically developing child is required to "prove" their knowledge of every vocabulary word they can utter.) We usually get stuck because most of my students will not consent to participate in assessment-style activities. They will produce inconsistent or meaningless responses because they simply cannot be motivated to identify a "fork" from a field of 4 pictures. And so, the skeptics tell me I cannot "assume they have the skills:" I have to teach them.

By presuming competence, I refuse to do either. My teaching does not assume that my student can identify a picture of a fork (or numbers, or whatever other vocabulary is in question.) Nor do I spend my time direct teaching basic pre-school vocabulary. I can teach the 8th grade math curriculum (geometry and equations) without knowing for certain if my student knows number symbols. Will I teach number symbols in the process? Absolutely. I can teach mid-grade literature without knowing if my students can identify so-called "functional" vocabulary or know what a "wh" question is. Will they learn that in the process? Probably. They'll also read some really good literature that is appropriate to their age. (Please don't get me started on "wh" questions - I have found that when most people say a student doesn't know "wh" questions they really mean the student doesn't have a certain level of general knowledge, which is generally to be expected of students with complex disabilities and fundamentally Not. The. Same. Thing. One is skill, the other is content. Can you guess which one I care about more?)

My students, like all other students, will use vocabulary to answer questions and create assignments. That will tell me what they know. I don't need them to identify pictures on an assessment they don't care about. I need them to use them in a meaningful context. My students, for whom formal language continues to be a weakness, will demonstrate comprehension of concepts in a myriad of non-linguistic ways, and I will accept those as equally valid measures of their comprehension. Because I understand that, especially for students just learning formal and symbolic language, the symbolic representation and the concept are not the same thing.

That is what Presuming Competence means to me. It means not letting the fact that I cannot prove whether or not a student knows a concept or has a skill through formal assessment hold me back from teaching them higher level materials. Simply put, it means believing that all students can learn and teaching them.

Friday, May 1, 2015

Prove it: A Post for BADD 2015

This is my post for Blogging Against Disabilism Day 2015. Read more posts here.

A kindergarden student, learning to read, gets periodic assessment of their reading, and based on those assessments, moves up or down in their reading instructional level.

Yet, when my nonverbal 13-year-old student, who is also learning to read, takes the same assessment and I say I am going to move her up in reading instructional level as a result, I am met with the following response:
1. assumption that I read the passage to her.
and/or
2. push-back that I must do many more assessments before I can say for certain that she can read at that level.

When I use the formal assessment tools built into our phonics program for assessing symbol/sound awareness with one of my students and comment to one of my colleagues that my student (a non-speaking 14-year old who communicates with a low-tech eye gaze board) seems to know his consonants and be ready to move on to learning CVC words, I get the following response:
1. questioning whether I am going to assess all the letters or “just the ones on this page?"
2. commenting that “well those are the hard ones” despite the fact that I clearly stated that the section needed to be gone back to, not because the student had struggled but because the student had fatigued in using his eye gaze system and needed a break.

Why? Because they are non-speaking and the concept that a non-speaking person who is not yet using formal communication could read is completely alien, even to my fellow professionals working in the field of severe special education.

If they had been a verbal, typically developing, kindergarden students, no one would have questioned the validity of the assessment results. Yet this happens all the time when instructing students with limited formal communication skills in the general curriculum.

Yet there is a hypocrisy here. Because there is one assessment that they only had to take once. It’s the most flawed assessment they ever took, not least because it was a language based assessment given to someone with no formal language. I’m referring of course to the IQ test. The test that showed all the things they couldn’t do. The test that provided the justification for an assessment and therapeutic based education instead of a standards-based  education. No one seems to have any problem taking the results of that single assessment at face value.

That is the heart of ableism. We are only comfortable with accepting with assessments of individuals with disabilities that show us how they are disabled; the ones that show us what they can’t do. (If that reading assessment had shown she couldn’t read it, I doubt anyone would have asked me to do more assessments to make sure I wasn’t wrong.) Show an assessment that challenges those assumptions, an assessment that shows how they are skilled, and people will refuse to believe it without additional irrefutable proof.