Category Archives: Visual Supports

Creating Visuals Instantly for Unpredictable Activities

As an adult with autism, knowing what will happen during each day is important to me. For children, who have much less life experience, it is often a deal breaker in terms of them being able to participate in life around them. Using visual schedules supports this need both at school and on ordinary days at home, but what about those times when life gets hectic or when spontaneity is in order?

Why Visuals Work
Having an autism neurology means that neither internal regulation (physical, sensory, emotions) nor external regulation (making sense of the world around us) just happens! We must bring deliberate and ongoing attention to these areas. Using a visual schedule and other visual supports are powerful in establishing a working external organization (Endow, 2011, pg. 65).

Supporting Your Child With Visuals
There are many ways you can support your child when you do not have his visual schedule with you or when you do not have the right picture to use on the visual schedule. Remember, it is not about the visual – it is about supporting your child. When one of those needs is to have the world outside his skin organized visually this can be accomplished in a variety of ways.

Creating Visuals Instantly
Here are some ideas:

1. Sticky Note Schedules: It is easy to have a pad of sticky notes in various places (purse, pocket, car, your child’s back pack, beach bag, etc.). Use sticky notes when you are not sure yourself just what will happen until it happens. For example, you are taking your kids to the beach. You do not know exactly what will happen in which order because it depends upon the circumstances you will encounter. Using sticky notes, you can print “driving to the beach” (or draw a car) on one note and “beach entrance” (or draw the entrance sign) on another sticky note. You have just created a First/Then schedule (Endow, 2011, pg. 71). Once you know what will happen next you can make the next sticky note piece of your schedule. Perhaps it will be “put the blanket down,” or if you do not need to be that detailed to support your child, “play in the water.”

2. Sticky Note Choices: It is also easy to use your sticky notes to give visual choices. If your child cannot figure out what to do once you have the blanket down you might use sticky notes to give the choice of swimming (draw waves) or playing in the sand (draw sand pail).

3. Check Off Task List: Sometimes you will have several things that need to be accomplished and you either don’t know the order you will do the tasks or if you will get them all done. You can make a list using paper and pencil, the Notes feature on your child’s iPad (or some similar device) or a small dry erase board. A check off or cross off schedule works great for outings where you know the components, but not the order (Endow, 2011, pg. 72). For example, at his brother’s baseball game your son will do several things before it is time to go home such as:

      • watch the game
      • play on the swing
      • purchase a treat from the concession stand
      • sit on the lawn chair
      • lay on the blanket
      • use the backpack toys
      • play iPod games
      • drink from the water bottle

A cross off schedule allows your child to see and to check off the accomplished items when he asks, “Is it time to go home yet?” It also gives him a visual idea of what else there is he might do during the ball game. When it is nearing time to leave you can tell your child to choose one more cross off activity and then it will be time to leave.

4. That’s-a-Surprise Cards: One child I worked with, Tamika, became quite disregulated and prone to meltdowns when too many events hit her as a surprise. Sometimes I could accurately guess a “surprise” registration such as a novel event. Other times I would not guess, such as when a truck passed as we were waiting to cross the street and Tamika was expecting only cars.

It isn’t the event that is important, it is the registration of the event as a surprise by the child’s nervous system. I knew that Tamika’s neurology could handle 3-4 of these “surprises,” but beyond that we were pushing our luck to have her remain calm without giving her nervous system some down time to reorganize.

Since Tamika was able to show whenever something hit her as a surprise I gave her three That’s-a-Surprise cards (recipe cards with an exclamation mark on them). She handed over one card each time she experienced a surprise. Once she had given me all three cards we would take a break from activity so Tamika could regulate, after which she got the three surprise cards back and the process started over.

5. When Nothing Else is Available, Use Fingers to Track Process: One time I arrived at a consultation to discover I was to accompany a student to the apple orchard. Jorge had never been to the apple orchard, nobody had prepped him, it wasn’t on his schedule and the van was leaving shortly! Upon arrival at the apple orchard I asked what the kids do there and then used my fingers as visuals going through the process saying the words to go with each with each finger like this:

      • “First (holding pointer finger), we will go for a walk.”
      • “Then (holding middle finger), we will pick our apples, putting them in the apple bag.”
      • “Next (holding ring finger), we will pay for the apples in our apple bag.”
      • “Then (holding pinky finger), we will carry our apples to the van.”
      • “At the end of the school day (holding thumb) we will each take our apples home.

I went over my five-finger visual system several times. Each time through Jorge made a verbal approximation of one additional item. Only after he understood all five items did he smile. Off we went! At each juncture I used my five-finger visual to highlight for Jorge just where we were in the apple orchard process.

Summary

If your child needs or benefits from the use of visuals know you can support him during the unpredictable nature of spontaneity even if you don’t know yourself what will happen ahead of time. While it is great to have computer-made visual schedules such as Boardmaker, know that sticky notes and recipe cards can come in quite handy. And when all else fails, you can fall back on your built in visual system of five fingers on each hand! Providing the visual support your child needs will go a long way to ensure both of you have more positive experiences while out and about in your community.

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BOOKS  BY JUDY ENDOW

Endow, J. (2019).  Autistically Thriving: Reading Comprehension, Conversational Engagement, and Living a Self-Determined Life Based on Autistic Neurology. Lancaster, PA: Judy Endow.

Endow, J. (2012). Learning the Hidden Curriculum: The Odyssey of One Autistic Adult. Shawnee Mission, KS: AAPC Publishing.

Endow, J. (2006).  Making Lemonade: Hints for Autism’s Helpers. Cambridge, WI: CBR Press.

Endow, J. (2013).  Painted Words: Aspects of Autism Translated. Cambridge, WI: CBR Press.

Endow, J. (2009).  Paper Words: Discovering and Living With My Autism. Shawnee Mission, KS: AAPC Publishing.

Endow, J. (2009).  Outsmarting Explosive Behavior: A Visual System of Support and Intervention for Individuals With Autism Spectrum Disorders. Shawnee Mission, KS: AAPC Publishing.

Endow, J. (2010).  Practical Solutions for Stabilizing Students With Classic Autism to Be Ready to Learn: Getting to Go. Shawnee Mission, KS: AAPC Publishing.

Myles, B. S., Endow, J., & Mayfield, M. (2013).  The Hidden Curriculum of Getting and Keeping a Job: Navigating the Social Landscape of Employment. Shawnee Mission, KS: AAPC Publishing.

Originally written for and published by Ollibean on August 11, 2014

More Than An Autism Diagnosis

I am an adult with autism. My thinking is visual rather than word-based. Autism gifts me with a literal and concrete way of thinking. My thoughts are all in full moving color. You can read about this and about my life in my book called Paper Words, Discovering and Living With My Autism. (Endow, 2009a)

“Always, I have a front row seat to watch the show! Each color, with its infinite variety of hues and brightness, has its own movement patterns and sound combinations. Even though spoken words are the medium most often used by people to communicate with me, I am wired to connect to these words through the sound and movement of colors. This is the way I think. It moves quite fast, but even so, tends to be slower than the speed of conversation. This can cause me to look less intelligent. People say I have processing delays. Painting allows me to show my thoughts without the burden of constant translation.” (Endow, 2013)

So, why am I telling you this?

I recently sent an email to friends telling them of my art expression through acrylic painting and inviting them to take a look at the Art Store page on my website with the paintings that show my autistic style of thinking. (www.judyendow.com)

After viewing the paintings along with the above quoted words that go with the paintings, a friend responded saying that I seemed to have connected with a part of myself that has very few adjectives in common with the stereotypical view of autism.

This got me thinking. Stereotypical views of autism are based on the neuro majority assignment of “truth” as they look at us.

All human beings, regardless of neurology, look out at the world through eyeglasses imposed upon them by their own neurology. Then, they assign meaning to the behavior of others according to the meaning that behavior would have were they engaged in it.

Most times this automatic guess is correct, but sometimes – like when neuro majorities are looking at autistics – the guess can be wrong. Over time, this repeated wrong guessing takes on a life of pseudo truth and becomes a stereotypical view. Thus, today we have a stereotypical view of autism that is quite narrow and limited and very much lacking in empathy, generated by those who live in their own world (that is not our world)…

Oh my goodness! Isn’t that precisely how neuro majorities describe us! Might it mean that we both – neuro majority and autistic – are making assumptions about the other according to our own yardstick measure that we unwittingly assume, without giving thought, is baseline “normal?”

The autism diagnostic criteria are a report on deviation from the typical neurology. As such it shows a picture of what autistics ARE NOT and highlights what we CANNOT DO as compared to the majority “normal.” It says nothing at all about who we ARE or what we CAN DO. Indeed, our abilities and skills most often remain untapped because the neuro majority does not possess them so have no way to understand or support that development in us. For example, if my way of thinking in the movement and sound of color had been supported as a youngster I likely would have been able to produce paintings long before my late 50’s.

Even so, the negative, deficit-based language of diagnostic criteria is not good or bad, right or wrong. In fact, it is necessary if we want to utilize health insurance to pay for treatment and support of autistic individuals. They must “have” something and that something must be something “wrong” in order for the health care reimbursement system to work.

The problem comes when we take the deficit-based language out of the diagnostic realm and start using it to define the humanity of individuals with autism. It imposes limits on the way people think about us and in turn on the opportunities they extend to us.

So my friend was almost exactly right when saying that, through my painting, I seemed to have connected to a part of myself that has very few adjectives in common with the stereotypical view of autism. I say, “almost exactly right” because I have not connected with this part of myself. This IS “myself” – always has been. The real of me – the essence of who I am as a human being – has very few adjectives in common with the stereotypical view of autism!

When talking about autistics – individuals who have been diagnosed with autism – it is important to realize your words have power, often opening or closing doors. What you say and how you say it really does matter. (Endow, 2009b) Please do not use the deficit-based diagnostic criteria of autism to describe my humanity – or the humanity of any autistic.

In this age of the stereotypical view of autistic people, mainly due to the autism awareness campaigns, here are some ideas to help any neuromajority person who may be interested to see beyond an autism diagnosis in an autistic person:

  • When interacting with an autistic think of that person rather than what you happen to know about autism. What you know about autism may or may not apply to a person with whom you are interacting. And even if it does apply, it will not do much for you in terms of getting to know that person.
  • Think of the person you are interacting with rather than the language pigeonholes you have heard applied to autism such as low-functioning and high-functioning. Nobody actually has a precise definition of those words. After all, how would you respond if someone asked you, “Are you high-functioning or low-functioning?”
  • Realize that autistics are measured against the majority “normal” in order to get a diagnosis and, if young enough, early intervention. This measure is one of “less than” as a diagnostic necessity, but please remember we are not “less than” human beings. We have a diagnosis – not a flawed humanity. We have different operating systems. This means we may struggle with many of your ways and have to overcome many obstacles to fit into your world, but we are not less than – just different.
  • Get to know us for what we can do rather than for the diagnostic criteria attached to our label. This may be hard because the majority of social conversation and news media reporting is laden with definitions of autism, which of necessity are deficit-based. This is what people have come to know about autism. It has become our “public image” so to speak. But at the end of the day don’t we all like to be known for our strengths – for what we can do rather than for our struggles? Don’t we all want to be seen in our best light as good human beings in this world?

White Thought Wave on GreenPainting is White Thought Wave on Green by Judy Endow

Note: Greeting cards along with prints in three sizes
available for purchase at the
Art Store on www.judyendow.com

BOOKS  BY JUDY ENDOW

Endow, J. (2019).  Autistically Thriving: Reading Comprehension, Conversational Engagement, and Living a Self-Determined Life Based on Autistic Neurology. Lancaster, PA: Judy Endow.

Endow, J. (2012). Learning the Hidden Curriculum: The Odyssey of One Autistic Adult. Shawnee Mission, KS: AAPC Publishing.

Endow, J. (2006).  Making Lemonade: Hints for Autism’s Helpers. Cambridge, WI: CBR Press.

Endow, J. (2013).  Painted Words: Aspects of Autism Translated. Cambridge, WI: CBR Press.

Endow, J. (2009).  Paper Words: Discovering and Living With My Autism. Shawnee Mission, KS: AAPC Publishing.

Endow, J. (2009).  Outsmarting Explosive Behavior: A Visual System of Support and Intervention for Individuals With Autism Spectrum Disorders. Shawnee Mission, KS: AAPC Publishing.

Endow, J. (2010).  Practical Solutions for Stabilizing Students With Classic Autism to Be Ready to Learn: Getting to Go. Shawnee Mission, KS: AAPC Publishing.

Myles, B. S., Endow, J., & Mayfield, M. (2013).  The Hidden Curriculum of Getting and Keeping a Job: Navigating the Social Landscape of Employment. Shawnee Mission, KS: AAPC Publishing.

Originally written for and published by Ollibean on April 16, 2014

Excerpt From Paper Words: Discovering and Living with My Autism

I remember with fondness my institutional social worker and some of my favorite aides who began group therapy sessions with a handful of girls on my ward.  The topic was often the same – FEELINGS.

I understood feelings intellectually, knowing their labels and their definitions.  I also began to realize that the way I perceived the world – through the movements and sounds of colors –

though real      as real

could be

to me

was not

a reality           shared

by others

and thus …

I came to understand that if I wanted one day to be discharged from this institution, it behooved me to NOT share my color realities with others.  So, I didn’t.

Instead, I focused on learning all I could about feelings so that I might figure out how to match this information to my perceived experiences with my beloved colors.  And yes, colors were my “beloved” because through the movements and sounds of colors I was able to make my way in the world outside of my skin.  Because of my perceptions of the ways of the colors all around me and the colors generated from the interactions between people, I began to pay more attention – and thus came to a better and better understanding of the world-people world all around me.  Thus, as a teen I was able to begin to very literally sort out and apply the feeling labels I carried around in my pocket to the colors of my then-current life experiences.

Today I write this because I want people to understand that actual barometer development happened in a very literal and concrete way for me.  I also would like it if people could start to imagine a world perceived by the movement and sounds of colors rather than a world whose meaning is primarily obtained by the sound of words being articulated.

And while you are imagining, please entertain the notion that a person who has an internally wired neurology to enable this, though a bit different from most, may not be any less intelligent, or indeed any less of a human being, than the typically wired folks, who are clearly in “The Majority” in the world-people world.

It may not be any better or any worse …

It is just different.

(But, for real, does “different” and “minority” need to be equated with “less than”?)

And still, at this point in the story, I had not yet become acquainted with autism.  Indeed, my “communicative” brand of autism had not yet become widely known in the world outside my skin.

But just because others didn’t yet know about IT

and therefore I could not be told about IT

or have any way to become acquainted with IT,

I nevertheless kept right on discovering this IT

that would one day come to be called my AUTISM

So,       once again,

come               along
with me

on my              journey
of discovery…

of my own       private
world               that resides

in that               inside space
of the place                 on

the side of
my skin            that’s located on

the inside
side of             me

this      private world
of mine

that would
one day

come to           be called

            my autism …

 Excerpt from Paper Words: Discovering and Living with My Autism, pp. 43-44

Note: All my thoughts are in pictures. Words are a translation of the pictures I use when thinking. The spaces between letters and words represent how long it takes for the pictures to fluidly move in such a manner as to connect smoothly with the next thought.

Paper-Words

BOOKS  BY JUDY ENDOW

Endow, J. (2019).  Autistically Thriving: Reading Comprehension, Conversational Engagement, and Living a Self-Determined Life Based on Autistic Neurology. Lancaster, PA: Judy Endow.

Endow, J. (2012). Learning the Hidden Curriculum: The Odyssey of One Autistic Adult. Shawnee Mission, KS: AAPC Publishing.

Endow, J. (2006).  Making Lemonade: Hints for Autism’s Helpers. Cambridge, WI: CBR Press.

Endow, J. (2013).  Painted Words: Aspects of Autism Translated. Cambridge, WI: CBR Press.

Endow, J. (2009).  Paper Words: Discovering and Living With My Autism. Shawnee Mission, KS: AAPC Publishing.

Endow, J. (2009).  Outsmarting Explosive Behavior: A Visual System of Support and Intervention for Individuals With Autism Spectrum Disorders. Shawnee Mission, KS: AAPC Publishing.

Endow, J. (2010).  Practical Solutions for Stabilizing Students With Classic Autism to Be Ready to Learn: Getting to Go. Shawnee Mission, KS: AAPC Publishing.

Myles, B. S., Endow, J., & Mayfield, M. (2013).  The Hidden Curriculum of Getting and Keeping a Job: Navigating the Social Landscape of Employment. Shawnee Mission, KS: AAPC Publishing.