Tag Archives: nonverbal communication

The One Where I Talk About Why Talking is Hard

February 6, 2014 musingsofanaspie 221 Comments

Today, I’m interrupting the sensory processing series to do something a little different. Okay, a lot different. I had originally planned to make a video blog about sensory diet to run today. What happened instead was a video about why talking is hard.

About 45 minutes into a very frustrating attempt at speaking on video, I gave up. I was ready to walk away from the process when The Scientist asked me to describe what I was feeling. Mostly I was feeling frustrated and angry with myself, but I eventually got past that and managed to talk a little about why I have so much difficulty speaking in this type of situation.

The short answer: The thinking and speaking parts of my brain seem to compete for resources, making it harder for me to organize my thoughts when I speak versus when I write. When I see how much I repeat myself in this video, I cringe, because if I were writing these thoughts out, I would use 1/3 as many words and probably be able to convey twice as much content.

If nothing else, I think you might find the contrast between my written communication and spoken communication interesting. Continue reading The One Where I Talk About Why Talking is Hard →

Communication

Silence III: Intention

November 8, 2013 musingsofanaspie 36 Comments

The Scientist and I have done another experiment. A twenty-four hour vow of silence. We began at noon on a Tuesday and finished at noon on Wednesday. The agreement was no spoken communication, but we would text if something urgent arose.

The first couple of hours were odd. I’ve never been intentionally silent simply to see what would happen. I’m comfortable with silence, but I felt like I was having to internalize a new rule, which made me a little tense. Also, there was the factor of the unknown. What would happen? Would we be able to sustain 24 hours of not talking?

After the first few hours, I felt myself start to settle internally. I love the sense of quiet that comes over me when I don’t have to speak or process spoken language for an extended period of time. It allows my internal processes to run uninterrupted. On a practical level, I’m more focused. Emotionally, I feel peaceful.

As the day wore on, I realized a few things:

A lot of what we say in the course of a day isn’t especially necessary. We speak as a touchstone or on impulse or without even thinking.
Without spoken communication, you have to pay a lot closer attention to the person you’re with. I thought it would be the opposite, that we’d feel disconnected. It turns out that not being able to shout from one room to the next about something forces you to be more intentional and aware.
I’m much more naturally inclined to silence than The Scientist is. That’s not surprising.
Being silent created a feeling of being present, focused and energized. I felt more mindful of my actions during the day.
Not being able to communicate complex ideas would get frustrating if I did this for more than a day. We managed to communicate simple things with gestures: time to walk the dog, meet you on the couch in five minutes to watch TV. Beyond that, I had little idea what The Scientist was thinking, which was strange and a bit disorienting.

We managed to make it the full twenty-four hours. Sort of. The Scientist had to take a work-related phone call and he volunteered to go pick up a package at our apartment building’s office. I slipped once and exclaimed “oh” when a man appeared out of the dark beside us as we were walking the dog at night.

All of those felt like reasonable exceptions to the experiment. We never did have to text each other about anything.

I now understand why monasteries that limit or prohibit talking have strict routines. We relied a lot on routine to navigate the day without speech. We always walk the dog after dinner. We always go to the gym on Wednesday morning. If not for those routines, it would have been harder to get on the same page about all the simple activities that fill up our days.

A caveat if you’re thinking about trying this at home: twenty-four hours of silence can drive you deeply inside yourself. The Scientist and I both agreed that we liked this part of the experience a lot. However, two days later I found myself experiencing some intense feelings that had surfaced as a result. If you decide to take your own 24-hour vow of silence, it’s a good idea to be sure you have a support network in place, in the event that you find yourself having a similar experience.

Like our other experiments, this one has taken on a permanent nature. We’ve decided that from now on, Mondays will be silent. I’m looking forward to seeing what the long-term effects of having one nonspeaking day a week will be. And, of course, I’ll be back to share the details.

Communication

Silence II: Variation

November 6, 2013 musingsofanaspie 41 Comments

I have more than one kind of silence. There is the very bad kind, the crushing kind. That one I could do without.

There is also the heavy silence. I can force the words to come out, but each one is an effort, like lobbing boulders out of a pit. They land in the dirt around me, scattered, muffled, obscured by clouds of dust. Lobbing boulders is hard work.

There is the accidental silence. The words fly away, leaving gestures, grunts, nothing at all. “Didn’t you see my eyes get wide?” I ask The Scientist when he wonders why I didn’t warn him about the wall he was about to back into.

There is the silence of too much. Too much input. Too much to process. Too many people, things, noises, questions, answers, objects, movement. I feel myself fading into the scenery, disappearing. I become silence itself. Continue reading Silence II: Variation →

Communication

Silence I: Frustration

November 4, 2013 musingsofanaspie 87 Comments

The first in a 3-part series on silence.

My silence is frustrating. For me. For others.

I don’t mean the silence between the words, the comfortable kind, the long drive in the car, relaxed lunch in the park, playing video games for hours side-by-side on the couch, reading together kind of silence.

Frustrating silence is the kind that arises in place of words, filling up all the space where the words should be. It starts with a heaviness in my chest, like my breastbone has become a plate of armor thick enough to stop a lance or a bullet or a barrage of charged emotions.

The weight holds the words down, tethered tight, floating out of reach. I can see them, hear them. Inside me, there is a cacophony of noise as the words rattle and clash, struggling to escape. It feels as if I’m shouting and yet there is no sound, except within me.

Then one breaks free. Two. Five. A phrase or a sentence. Small and inadequate to the task, they float up, fill with breath, are shaped by tongue and lips. Often the ones that escape are the most practiced. Scripts. Platitudes. The reliable “I don’t know.” Continue reading Silence I: Frustration →

Communication

Saying No

July 11, 2013 musingsofanaspie 68 Comments

Saying “no” is hard. Often when I say no, I feel like I’m disappointing the other person, like I’ve somehow failed.

This probably sounds funny coming from someone who not too long ago wrote about her “no reflex” but there are two categories of no for me. There’s the reactive no–the one that just pops out because I can’t deal with change or spontaneity. I might feel momentarily bad but don’t get all twisted up inside over it.

The other no–the one that hides and cowers and wakes up the butterflies in my stomach with its nervous pacing–is the no that makes me feel like I’m failing. The hard no is often a result of tension between what the other person wants and what I can feel like I can reasonably do. It’s often tied in with adult social obligations, the sort encountered by parents, spouses, adult children, employees: the neighborhood book club, the PTA committee, the office holiday party, the class research project.

When people ask others to join, volunteer, lead or otherwise participate in something, they do it with such a hopeful, expectant tone of voice. The implication is “how can you refuse this excellent thing that we’re all counting on you to be a part of?” And so often, that excellent thing just feels like a burden to me.

Saying no, however, is going to lead people to make assumptions. I’m not pulling my weight. I’m standoffish. We’re not as close as they assumed. I think I’m better than other people. I just don’t care.

All of the other moms are on a committee. All of the other parents have coached a season of rec sports. All of the other wives will be there. All of the other cousins are going to the wedding. All of the other students in the department are attending graduation. All of the other neighbors are baking for the fundraiser.

Of course not literally all of the other ______ are doing anything, but that’s what the person asking will imply. Everyone else is doing it, what aren’t you? Or worse, not enough people are doing it, I’m counting on you to help me out.

This is peer pressure at its most insidious. The hints that doing this thing makes you normal or a better person or not a bad person are powerful, especially when you’ve been raised and socialized to feel like fitting in and being normal are a primary goal.

And here is where we come to the crux of the issue. Autistic children are often grow up with a strong desire to fit in, to be liked, to be normal and/or to not get into trouble. We aren’t necessarily taught that we have the right to decline activities that uncomfortable or that we can sometimes put our needs first.

Learning to Say No

No comes from different places for different people. Strong boundaries. Good social skills. Explicit instruction in saying no as a child. Good self-esteem. A general orneriness.

If no doesn’t come naturally or has been socialized out of us, we can still learn to say no. This is where scripts come in handy. Not only do scripts give us the words that we might find unnatural, they prevent us from accidentally saying yes when we mean no.

Social communication is fraught with code words and unspoken communication. If your no is too soft, it can be misconstrued as a yes. For example, if you mean “no” don’t say “I don’t think so” or “I shouldn’t.” This can be interpreted by the other person as an open invitation to persuasion, negotiation or further discussion. You may find yourself feeling bullied into a “yes” when you already thought you’d said no.

If you mean no, unless you clearly and unambiguously say “no” the other person may think you’re being polite or coy.

But how to do that?

Saying No 101

I’ve always secretly wished there were social skills classes for adults. Then, recently, I realized there is something very similar: etiquette. On a whim, I’d checked Emily Post’s aptly titled Etiquette out of the library. And guess what? It’s loaded with not just advice but scripts. Lots and lots of them.

Emily Post and the people who now edit her books have spent a great deal of time figuring out the polite thing to say in just about every imaginable situation. Did you know that saying no can be as simple as:

“Would you like to come with us to lunch?”

“No, but thank you for inviting me.”

That’s right, you can simply say “No, but thank you for [asking, inviting, including, thinking of] me.” No further explanation necessary! This was a revelation to me because I always thought I needed to provide an excuse when declining an invitation.

You can, of course provide an (honest) excuse if you have one:

“No, I have plans for this weekend, but maybe next time.”

“No, I can’t make it this time. Work/school is too hectic.”

When providing an excuse, be careful not to put off for the future something you have no intention of ever doing. Saying, “Work is really busy right now” opens the door to getting the same request next week. If the request is something you don’t want to do, remove the invitation for a repeat inquiry by saying, “My schedule is full right now. If that changes, I’ll let you know.

And for those of us with food sensitivities and allergies, here are a couple of simple, polite phrases for declining food offered by a host(ess):

For foods you don’t like, a simple “no, thank you” is fine.

For allergies, intolerances or diet restrictions, you can say, “________ is off limits for me, but everything else is wonderful.“

Polite. Straightforward. Inoffensive to your host’s cooking. Again, no need to offer a lengthy explanation or get into why you couldn’t possibly put a single piece of creamed spinach in your mouth without dying of sensory overload.

Beware of Traps

Not everyone knows how to politely take no for answer. People often try to guilt or bully others into saying yes, even after they’ve said no. Don’t fall for mind games:

Just because someone compliments you, you don’t have to say yes to the request that follows. For example, Mary says, “You’re the best web designer/babysitter/cake baker in the world. I know this is last minute, but could you [do some task that you don’t have time or energy for]?” Instead of feeling flattered/guilted into saying yes, you can say, “Thank you, but I don’t have time right now.” Politely acknowledge the compliment, then follow with a firm unapologetic no.
Peer pressure doesn’t end in high school. If someone prefaces a request with “Everyone is . . .” or “You’ve got to . . . ” beware. Don’t cave in to the bullying–instead politely decline with a simple, “I can’t right now.” Repeat as necessary.
Don’t allow others to trick you into doing something by making you feel sorry for them. A simple “I’m sorry you’re feeling overwhelmed, but I have my own deadlines to meet” is sufficient for turning down an unreasonable or inappropriate request.

Even well meaning people sometimes have trouble taking no for an answer, as Mados vividly illustrated in her recent post “Parties & Irrelevant Pity“. Saying no can be a complex social exchange and one that requires a lot of practice to do well. Scripts like the ones Emily Post suggests are a good starting place, especially for those of us who struggle with how to phrase things as well as how to maintain boundaries.

Communication

(Not) a Little Slow

May 29, 2013 musingsofanaspie 116 Comments

There is a moment I dread in conversations with strangers: the moment when that stranger–that person I’ve been talking to for a minute or two or five–decides I’m “a little slow.”

It doesn’t happen with every stranger, but it happens often enough that I can pinpoint the moment a conversation turns. To start, we’re both on our best interacting-with-a-stranger behavior, a bit wary, a bit too friendly, whatever. Then I slip. I miss some key bit of information, ask the other person to repeat something one too many times, stutter, backtrack, repeat myself, interrupt again, lose the thread of the conversation, take a joke literally, perseverate. There are a lot of ways it could play out.

The response–the one that makes my skin heat up and my heart race and the blood in my ears pound–is subtle but sudden.

A note of condescension slips into the other person’s voice. I may suck at reading body language, but I’m pretty good at gauging voice tone. Maybe they start speaking more slowly or repeating themselves. They downgrade their vocabulary to smaller words. They repeatedly ask questions like, “are you following me?” and “does that make sense?” They get pedantic, having decided I require some sort of instruction.

In short, they’ve decided I’m a little slow on the uptake.

At the first sign of this shift, I get a sick feeling in the pit of my stomach. I’ve been categorized by this person who knows next to nothing about me and is forming an opinion based on my spotty verbal skills, tallying them up with my inconsistent eye contact and my incongruent body language and all the other ways my body says “not like you.”

Am I Slow?

Literally speaking, I guess I am. My verbal processing–both receptive and expressive–is impaired to the point that I often need more time than the average person to understand or respond to someone.

I have all sorts of communication glitches. I struggle with verbal instructions. If there’s background noise or other distractions, my auditory processing lags to the point that it can take a few seconds to process speech from noise into words. My verbal responses default to scripts–sometimes not even the right scripts–or become minimal when the conversation takes an unexpected turn, moves too fast or is too unstructured.

There is a significant disconnect between my verbal skills and my intelligence or literacy or whatever you want to call it.

In short, I look better on paper. If I was a shelter pup, there would be a note in my file that said, “Does not show well.”

Generally, this isn’t a problem for me. I’ve engineered my work life so that I first “meet” people via email or some other text-based correspondence. By the time we talk on the phone or meet in person, the other person has (hopefully) formed an opinion of me that will withstand some verbal glitching.

I’ve gravitated toward text-based medium in general, spending my days working primarily with the written word. Still, I have to do things like go to the doctor, contact the super in my building for repairs, and navigate the university records office to correct my transcript–all situations in which I’ve encountered the dreaded conversation shift. Situations in which I went from feeling like I was on equal footing with another adult to feeling patronized, belittled or ignored.

And here’s the thing: I am an adult. Whether I speak eloquently and fluently or not, I’m still an adult. My ability to communicate verbally has no impact on my ability to understand the way a ground fault interrupter works or what the risk factors for breast cancer are or how to read my college transcript. I don’t need to have these things explained to me like I’m a child.

What do I need, you might be thinking? My wishlist:

Treat me like a competent adult.
Be patient. I might need a little extra time to compose my answer or to process what you’ve said.
If I ask for clarification, try explaining in a different way. If I didn’t understand the way you explained the first time, an exact repetition probably won’t help.
Assume that if I don’t understand something, I’ll say so.
Don’t rely on my body language or other typical cues for feedback about whether I understand what you’re saying. Unless you’re also autistic or know me very well, you probably can’t read my body language any better than I can read yours.
Give me time to write down key information if I need to.
Don’t oversimplify your language or speak unusually slowly or loudly.
If you’re giving me verbal instructions, break them down into specific steps and explain one step at a time.
If I keep repeating a question or statement, I need a stronger acknowledgement that you’ve heard and understood me.
Treat me like a competent adult.

Some of the stuff on that list comes under the heading of accommodations. These are things I have to ask for because they are outside the norm and others may not know that I find them helpful.

But some of it–like #1 and #7–those should be the bare minimum we can expect when interacting with other adults, regardless of how typically or atypically we present.

Communication

Is there a Link Between ASD Motor Skill Deficits and Social Communication Difficulties?

March 21, 2013 musingsofanaspie 63 Comments

I started this post thinking it would be about dyspraxia and Asperger’s. Dyspraxia, difficulty with fine and gross motor coordination, is often diagnosed alongside ASD. Adult symptoms of dyspraxia overlap with adult ASD traits to the point that even the experts have trouble separating the two. In fact, autistic individuals are sometimes misdiagnosed as dyspraxic.

If the experts are confused, I’m certainly not going to untangle the topic in a single blog post, so I decided to set that idea aside and write about general movement difficulties. Aspies are a notoriously clumsy lot. I’m forever tripping over stuff, bumping into stuff, dropping stuff, breaking stuff.

Seriously, if you like your stuff, keep me away from it.

I’ve broken an entire kitchen’s worth of glassware in my lifetime. In the first month of owning a new blender, I broke the glass pitcher not once, but twice. You’d think I would have learned the first time not to put it down so forcefully on the counter. After the second one shattered, I downgraded to a plastic pitcher because a blender is not worth that kind of trauma.

Gross and Fine Motor Impairment is Nearly Universal in ASD

The theories about why aspies are so uncoordinated are many: motor planning deficit, motor development delay, motor timing impairment, problems with initiation or inhibition, imitation and praxis impairments, deficient postural control, under reliance on feedforward control. There are also a handful of other conditions that muddy the waters further: apraxia, ataxia, hypotonia, dysgraphia, dyscalculia, dyskinesia . . .

You see where this is going, right? It would be easy to write a book on the subject and still not cover everything. Just defining all of those things would require a whole series of blog posts.

There are a few things that most of the experts agree on:

Some level of gross and fine motor impairment is nearly universal in people on the spectrum.
Motor impairments may improve somewhat with age, but generally persist into adulthood.
With more study, motor development delays could be a reliable indicator of the presence of ASD in very young children.
It is unclear whether dyspraxia is a separate diagnosis or the features of dyspraxia overlap with features of ASD.
The cause of motor development delay in autism is unknown.

It’s interesting that once again we have something (like insomnia) that occurs in the majority of autistic people but is not part of the diagnostic criteria. Autistic children routinely receive occupational therapy to improve their fine motor coordination, balance and posture; motor impairment is nearly universal. So why isn’t fine/gross motor skill impairment officially one of the diagnostic criteria?

What if Motor Impairments are Connected to More Than Clumsiness?

Some of the research I read about motor skill impairment in ASD is more radical than what you’ll find in the popular literature. Consider these two possibilities:

1. Delayed or nonexistent speech may be the result of a movement disorder. Rather than assuming that nonspeaking autistic individuals don’t have the cognitive development necessary for communication, some researchers believe that there is a physical impediment to performing the necessary movements with the mouth to produce speech.

This isn’t a blanket explanation for all situations in which autistic people are nonspeaking, but it does offer an alternative way of thinking about the relationship between speech and communication. Once we separate the two, thinking of speech in the physical rather than purely cognitive realm, we’re less likely to assume that because a person doesn’t communicate via speech they are incapable of communication.

It also presents another way of looking at the phenomenon of “selective mutism” (temporary loss of speech). Often a temporary loss of speech in autistic individuals is related to a period of high stress. When I’m very stressed, my speech suffers and I can become temporarily mute or significantly impaired.

I also know that during periods of intense stress, I’m more likely to trip and fall while running or to drop things. There is a definite deterioration in my motor coordination under stress. It’s not hard to imagine this extending to the motor aspects of speech.

2. Social communication issues may arise from early difficulties with motor skills. Before children speak, they rely on nonverbal communication for play. If autistic youngsters aren’t modeling the expected nonverbal cues due to motor impairments, they will also fail to receive appropriate nonverbal responses from their peers.

This failure to communicate physically may mean that autistic children have fewer and poorer quality nonverbal interactions with peers and therefore struggle to learn social communication at the most basic levels. As they grow older and nonverbal communication grows more complex, they fall further and further behind.

Facial expressions, hand gestures, posture and body positioning–all physical movements–are the primary tools of nonverbal interaction. If autistic individuals have difficulties with initiating, performing, mirroring, inhibiting or planning physical movement, it stands to reason that this would include difficulties with the physical movements inherent in nonverbal communication.

Social Communication Difficulties in a New Light

It’s interesting to think about social communication and speech difficulties as rooted in impaired motor skills. What if we struggle with speech and nonverbal social communication for the same reason that we struggle with catching a ball or learning to ride a bike?

Is it possible that a group of seemingly disconnected autistic traits have a common root in our motor skills impairment?

Communication

Writing is Communication Too

October 26, 2012 musingsofanaspie 27 Comments

If you get a group of writers together, on the internet or in a workshop, someone will eventually ask the ultimate navel-gazing question: why do we write?

My stock answer–the one that’s easiest to explain and makes me look least weird–is that I write because I enjoy it. There’s nothing like the rush of chasing an idea, my fingers flying across the keyboard, barely able to keep pace with my thoughts. There’s no other activity I can get so completely lost in.

That answer saves me from having to reveal this: I write to set the words in my head free.

My brain latches onto interesting ideas in a way that makes it hard to stop thinking about them. Once something grabs my attention, my mind will turn it around and around, shaping and growing it like a vase on a potter’s wheel. Writing the idea down stops the rapid spinning of the wheel and leaves me with the equivalent of a finished vase I can share with other people instead of a hard lump of clay sitting in my brain.

Shaping an idea in my head feels like this:

Ultimately, I write because I need to. I communicate better through written words than spoken words. When I write, I can take as much time as I like to shape my thoughts into a coherent whole. I can get feedback from others to check for clarity. I can let an idea breathe and grow over days or weeks.

The process is something like this: Write. Revise. Reconsider. Delete. Edit. Clarify. Rethink. Shape. Walk away. Come back. Write more. Think more. Print it. Read it. Share it. Revise, revise, revise. Done. Mmm, maybe just change that word. Or this one. Okay, really done. Yeah? Yeah.

Doing this in a spoken conversation is impossible. There’s no delete button for spoken words. Revising, in the form of explanations and clarifications, is rarely successful. Once you say something, it’s out there in a way that is, ironically, indelible.

Communication Deficit or Communication Difference

So do I have a communication deficit? (one of the core diagnostic criteria for Asperger’s)

That may depend on how we define communication. You could argue that writing is a one-way process. I carefully shape my idea and put it out there, feeling quite content with how it looks and feels, and then I go on my merry way, chasing another bright shiny idea.

It’s all very neat and tidy. It’s also very autistic. What could be more characteristic of an aspie than a one-way information dump followed by a determined retreat back inside my head to ponder the mysteries of the universe, or at least the mystery of why someone keeps leaving sandwiches on the sidewalk of one particular street where I walk my dog?

But, short of a mind meld, writing is my best shot at sharing what I want to say. I could talk all day and not get across half of what I can communicate in writing. Since I’ve started blogging, I’ve shared things with my family–in writing–that we’ve never talked about. Big important things and little niggling things, all of them left unspoken, sometimes for many years.

The result has been anything but one-way. Sharing my thoughts in writing creates an opening for others to start conversations, to ask questions, to offer insights and to share their own thoughts. This is communication–deep, fulfilling, nontraditional communication–in a way that I’ve rarely experienced.

It feels so good to share something with my husband and see a light of understanding in his eyes. It’s done wonders for our relationship to revisit past hurts and misunderstandings in a fresh light. There’s a new level of understanding opening up and I think it’s because I’m finally able to communicate, really communicate, how I experience and process the world around me.

I’ve also discovered that writing is a way to communicate with myself. The process of exploring Asperger’s is helping me integrate disparate parts of myself into a whole. It’s creating a map of my inner landscape in a way that is profoundly healing and empowering.

Perhaps this is what I meant when I said I write because I need to. Writing connects me to those around me, and it connects me to myself.

Once a Writer, Always a Writer

This is one the first things I ever wrote, when I was seven. I remember hearing my mother telling parts of this election day story to someone and deciding that I wanted to make it into a book. I still have it, in all its stained, stapled glory, and thought it would be fun to share.