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COMPARING THE MILLER METHOD WITH OTHER APPROACHES
How does the Miller Method differ from Greenspan's Floor Time Approach?

 
What do behavior therapists mean when - referring to the behavior of a child on the autism spectrum -- they say, 'If it walks like a duck and quacks like a duck, it's a duck!'?"

 
Why doesn't the Miller Method use "time out" to control children's disordered behavior?

 
Why does the Miller Method discourage the use of the term "Good job!" when a child does something desirable? What does it use in its place?

 
My autistic son is obsessed with balls.  When I take them away or hide them he cries inconsolably.  My behavioral consultant recommends that I get rid of the balls.  What would you suggest?

 
UNIQUE FEATURES OF THE MILLER METHOD
Where can I find the best, reasonably short but detailed explanation of the Miller Method?

 
Why does the Miller Method develop new rituals with children on the autism spectrum? Since these children already have plenty rituals, wouldn't giving them more rituals make them more autistic?

 
If I use sign language with my nonverbal child with autism will he become so dependent on it that he will never learn to use spoken language?

 
Why do you have children on the autism spectrum walk on an "Elevated Square" 2.5 feet above the ground?

 
THE MILLER METHOD WITH TANTRUMS
Major tantrum in department store. The tantrum in the department store yesterday occurred when 7-year old Benny—a child on the autism spectrum—let go of two balloons he was holding and they went 20 feet up to the roof. He wanted those balloons. There were many others to be had the same color so i got him two more, but of course this did not do. He kept yelling "need help" which is his favorite chunk phrase these days and freaked out, yelling and going after me as I tried to get him out of the store. It was bad, but I did everything I could think of. I stretched my arms up and said, "It's too high, can't get it, gave him two more. Any ideas, that could be helpful in this kind of situation?

 
My nonverbal 4-year old son (diagnosed PDD) always has a hardtime separating from me, his mom, to go on the bus for preschool.  Getting on that is is like torture for the poor little guy.  Any suggestions?

 
Shedding Light on the Subject!—My seven year old limited verbal child (on the autism spectrum) becomes distressed in movie theatres yet enjoys watching television at home. When taken to Sea World and Disney World he becomes very upset  when taken into a dark enclosure or tunnel and begins crying and stating No! Out! until he is taken back outside.  Why does he react like this?

 
My little girl with special needs (26 months) screams and tantrums when she has to leave the bathroom or kitchen to go to her room. What can I do to help her?

 
THE MILLER METHOD APPLIED TO PARTICULAR PROBLEMS
Is there some way you can teach an autistic child to hide while playing Hide and Seek? My child is fine with "finding," but seems to find it difficult to learn hiding. I suppose one of us will have to take him with us and hide to teach him to hide. Is there any other way?

 
How can you encourage a child to write and recognize her own name?

 
Why would our nonverbal autistic son be able to speak clearly in complete sentences when very unhappy but not at other times? For example, when he was led away from us to be evaluated by our child study team, the team clearly heard him say "I want Mommy" 2) When he fell and x-rays were necessary his father heard him clearly say "I want to go home". Can you shed any light on this rare speech?

 
Do you ever use swings in your method? Do you know of any research done on the effectiveness of swinging for autism?

 
GENERAL QUESTIONS
What is Cognitive and language development? What are the different ways in which this affects the children?

 
If a parent called me and stated that the doctor said that her child has "spectrum disorder," what is it?

 
There are no Miller Method programs where I live in British Columbia. Is there any way you can guide me in using your approach so that I can help my 5-year old autistic son?

 
How is language development affected by autism?

 
I read an article by Arnold and Eileen Eller-Miller that Temple Grandin referenced regarding the use of a visualized reading method. Is this method still in use? Is it suitable for reading instruction with a student with autism who has limited expressive but good receptive language?

 


COMPARING THE MILLER METHOD WITH OTHER APPROACHES


How does the Miller Method differ from Greenspan's Floor Time Approach?
While the two approaches are similar in their emphasis on transforming developmentally challenged children's repetitive and stereotypic actions into functional behavior whenenver possible, there are significant differences between the two approaches.

Greenspan's Floor Time approach is unstructured in that the therapist waits for the child's lead before attempting to build on it with "circles of communication." While also exploiting the child's leads, the Miller Method, in addition , introduces a specific program to directly address developmental lags. For example, if a child has never gone through the 9-11 month old stage of "experimentally" dropping things to learn how they fall, a Miller Method therapist may deliberately introduce a dropping system by showing the child how to drop things so that they land with a satisfying "clunk" in a pan and will then shift that pan so that the child learns to drop in different locations and with different people...The Miller Method also structures the children's behavior with the help of elevated structures such as the Elevated Square in a way that helps "scattered" children focus more effectively. For other differences see our book From Ritual to Repertoire or our chapter in the ICDL Guide to Clinical Practice edited by Greenspan and Weider and available next month (November, 2000).

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What do behavior therapists mean when - referring to the behavior of a child on the autism spectrum -- they say, 'If it walks like a duck and quacks like a duck, it's a duck!'?"
What they are saying, for example, is that if a child gives the outer appearance -- by correctly enunciating words -- of knowing what he or she is saying or reading, then, indeed, that child has this understanding -- We have a major problem with this formulation as applied to children on the autism spectrum -- or for that matter when applied to any child.

We have seen far too many children with autism utter spoken words perfectly or even seem to "read" complex sentences and yet totally lack understanding of what they are saying or reading, to accept the "duck" analogy. In other words, like the walking and quacking ducks that turn out to be decoys, these children may seem to be communicating or getting meaning from printed words, but really are not.

Being able to say the words correctly is one part of the job. But, only when the child truly understands everything that he or she says or reads -- and can demonstrate that understanding -- does the child have a foundation on which to advance cognitively and academically. Such progress is a major goal of the Miller Method.

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Why doesn't the Miller Method use "time out" to control children's disordered behavior?
We view "time out" as punishment for a child's unacceptable behavior as both inappropriate and ineffective with children on the autism spectrum.

First, there is no certainty that the child associates the time out with his or her previous unacceptable behavior. Second, given the fact that a major aspect of autism is the child's difficulty making human contact, it is difficult to see how placing a child in a time out room does anything but support the child's disposition toward autistic withdrawl.

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Why does the Miller Method discourage the use of the term "Good job!" when a child does something desirable? What does it use in its place?
We discourage the use of the term "Good job!" for several reasons: One, it's a pretty abstract term and even if it were understood by the nonverbal children who hear it, it's frequent repetition would soon turn it into meaningless jargon - as happens with any term that is frequently repeated. Instead of endlessly saying "Good job!" we find that narrating what the child is doing (like a sports announcer) is far more important for the child.

When one tells a child that he or she is climbing, jumping, peddling his or her bike, and so forth, those narrated words provide the child with a chance to relate the words he or she hears to what he or she is doing. This develops receptive language and can lead to the child learning to talk to himself or herself - a necessary prelude to being able to communicate with others.

Perhaps the only good thing about saying "Good job!" is the positive feeling conveyed by teacher or therapist through the voice. However, this same positive feeling can easily be conveyed while narrating with pleasure the behavior the child is performing.

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My autistic son is obsessed with balls.  When I take them away or hide them he cries inconsolably.  My behavioral consultant recommends that I get rid of the balls.   What would you suggest?
First, let me say that our philosophy is - whenever possible - not to take things away from the children but to try to build on what they have.  For your "ritual-captured" child, involvement with balls is an important system.  Repetitive play with them is at this time the very best that he can do with these intriguing objects.

So I would recommend trying the following:

Get all kinds of balls - big ones, little ones, red, green and yellow, soft, hard, heavy,  light - then set up different locations so the little balls go in one place, the big ones in another place.  Then -- before he gets bored with this sorting task -- start pelting him with the light (nerf) balls to start a ball interaction (like a snow ball fight). where you pelt him, he pelts you. Perhaps you get his father or another sibling to help him pelt you with the balls.  Periodically duck behind some furniture so he can't see you then suddenly reappear and pelt him again. If he ducks down wait until he pops up then get him again.  See if he will try to get you as you move from one hiding place to another..

After a time (when you judge he's had enough excitement) tell him its time to put the balls away.  Then, sing the "Clean up!" song as you point to the different balls all over the room and guide him toward dropping them in their proper location.  If, at that point, he wants to take a couple of balls with him as he prepares for bed, that's fine.  

I'm sure that as you follow this line of thinking you'll find other productive ways of turning his "obsession" into important interactive play that will prepare him for playing with other children. A.M.

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UNIQUE FEATURES OF THE MILLER METHOD


Where can I find the best, reasonably short but detailed explanation of the Miller Method?
Thank you for your interest in the Miller Method. There is now an excellent summary chapter on the Miller Method on the internet and available for download. Click on the icon below to download the PDF:



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Why does the Miller Method develop new rituals with children on the autism spectrum? Since these children already have plenty rituals, wouldn't giving them more rituals make them more autistic?
Good question. In answering it, let me first describe all the good things that introducing and working with rituals does for children with autism -- Suppose you have a tantrumming autistic child. Introducing a repetitive ritual of some kind -- having him or her go up and down stairs, cross back and forth over an elevated structure, repeatedly pour water or drop objects in a can, scribble back and forth, knock blocks off a stand, and so forth can often help calm the child and make it possible to bring him or her back into regular classroom or therapy activities in a relatively short period of time.

We are also able to vary the child's rituals (or systems as we call them) so that they become less and less like rituals and more like typical functioning. We expand them bit by bit, involve different people in them so they are no longer solitary and we can interrupt them in a way which induces the child to produce words, signs or actions indicating his or her need to maintain the ritual. So, far from adding to the child's autism, the systematic use of rituals (systems) turns out to be a powerful way of helping children on the spectrum begin to move beyond rituals to function more appropriately with people.

For further information on how the Miller Method works with rituals, read our book "From Ritual to Repertoire" published by John Wiley and Sons and available from www.cognitivedesigns.com

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If I use sign language with my nonverbal child with autism will he become so dependent on it that he will never learn to use spoken language?
A number of parents have expressed this concern about sign language. The plain answer is "No!". The use of sign language does not interfere with the development of spoken language. Quite the contrary, our research and that of others clearly demonstrates that children who previously could not follow spoken directions could do so after spoken words were paired with manual signs.

In other words, the meaning of the signs had transferred to the spoken words in a way that made heard spoken words meaningful. Also, for a certain number of children, the use of manual signs seems to "pull" spoken language. For these children - as for typical children - the manual signs are an important transition to functional spoken language.

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Why do you have children on the autism spectrum walk on an "Elevated Square" 2.5 feet above the ground?
We have been using elevation with children on the autism spectrum for over thirty years - ever since we discovered that children placed on elevated structures become more aware of themselves, produce better eye contact are more focused and able to communicate and to learn.

Further, we have found that a number of children who toe-walk on the ground walk completely flat-footed when elevated. We are gratified to find that there are now dozens of Centers using elevation around the country and in other countries.

Currently, a comprehensive controlled study contrasting the effect of functioning while elevated with comparable functioning on the ground is under way at the Language and Cognitive Development Center in Boston.

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THE MILLER METHOD WITH TANTRUMS


Major tantrum in department store. The tantrum in the department store yesterday occurred when 7-year old Benny—a child on the autism spectrum—let go of two balloons he was holding and they went 20 feet up to the roof. He wanted those balloons. There were many others to be had the same color so i got him two more, but of course this did not do. He kept yelling "need help" which is his favorite chunk phrase these days and freaked out, yelling and going after me as I tried to get him out of the store. It was bad, but I did everything I could think of. I stretched my arms up and said, "It's too high, can't get it, gave him two more. Any ideas, that could be helpful in this kind of situation?
Dr. Miller's response. The department store reaction sounded quite rough although I thought you handled it quite well. Getting the two balloons of the same color was absolutely correct. The only other thing that might have helped would have been attaching very long strings to the new balloons and letting the balloons sail away the way the first two did. Only this time, since there were strings attached to them, Ben could have the great joy of pulling the two new ones in. While doing that he would almost certainly forget about his loss of the first two balloons. Let me know how this suggestion plays out with him.
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My nonverbal 4-year old son (diagnosed PDD) always has a hardtime separating from me, his mom, to go on the bus for preschool.  Getting on that is is like torture for the poor little guy.  Any suggestions?
It may be that your son feels that when he leaves you to get on the bus he will never see you again.  In other words, that he has not yet gotten the notion that even though he leaves you he will eventually return to you.  For him, it is likely that when he is with you that the teacher at school doesn't exist and when he is in school that you don't exist.  If this is correct, then finding ways to help him connect his mom-at-home reality with the teacher-at-school reality, should ease the problem. 

One way to do this is to set up a picture sequence showing him going on the bus, going to school on the bus, getting off to go to school, being in preschool with his teacher, then leaving teacher and school to go on the bus, getting off the bus to be happily greeted by you. You should have one of these sequences and his teacher the other so you can work the going to school on the bus while the teacher can workgoing home to you on the bus.

Another thing that might help is giving him some item that he associates with you to take with him on the bus ( a kerchief, a pin, etc) .  At school the teacher can give him something from school to take home.  To further help him connect these two parts of his life it would help to have a large picture of his teacher at home (so you can call his attention to it)  and a large picture of you at school so that his teacher can refer to your picture (and your continued existence) even when you are not physically present.  A.M.

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Shedding Light on the Subject!—My seven year old limited verbal child (on the autism spectrum) becomes distressed in movie theatres yet enjoys watching television at home. When taken to Sea World and Disney World he becomes very upset  when taken into a dark enclosure or tunnel and begins crying and stating No! Out! until he is taken back outside.  Why does he react like this?
Many chlidren on the autism spectrum have a "fuzzy" sense of their own existence.  In the dark, enclosed settings you describe your son may become frightened because he loses visual contact with his own body (can't see his feet, etc.).  Such children (like many small, typical kids)  often need a night light at bedtime.  A small pen flashlight that your son can shine on himself could be very reassuring to him (but possibly annoying to others!) in dark places.
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My little girl with special needs (26 months) screams and tantrums when she has to leave the bathroom or kitchen to go to her room. What can I do to help her?
For your daughter the different spaces in your home are very disconnected from each other. That means leaving the familiar space of bathroom and kitchen must be for her like "walking off the end of the earth." You can do several things to help guide her to other spaces in your home: One effective strategy is to cut out foot prints the size of her feet and lay them out from where she is to where she needs to go. then have her simply walk on her footprints. You can also show her that she can venture from a familiar space for a few feet and then return to it. Then, keep expanding the distance until she has made contact with another familiar space. Once she develops an "inner plan" for the geography of your home, distress and tantrums at leaving one space for another should disappear.
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THE MILLER METHOD APPLIED TO PARTICULAR PROBLEMS


Is there some way you can teach an autistic child to hide while playing Hide and Seek? My child is fine with "finding," but seems to find it difficult to learn hiding. I suppose one of us will have to take him with us and hide to teach him to hide. Is there any other way ?
To teach your child to hide think of his hiding as an extension of the "peek-a-boo" game (which you tell me he already plays). First you put something over your face and he "discovers" you. Then he puts something over his face (hides) and then you "find" him. Then, extend the duration of his time behind the cover bit by bit before you "find" him. While he is behind the cover you can tell him how you are looking everywhere (but whre he is sitting) until you "find" him. Then, repeat the procedure with someone else putting him in more concealed hiding places. Then, let him hear about all the places where you are looking until you "find" him. After he is placed in and experiences a number of hiding places, he will have these hiding places from which to choose. I think he will get the idea from this. When he picks a new place to hide on his own you are really on your way. Have fun!
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How can you encourage a child to write and recognize her own name?
There are two ways in which you might be able to get your child to write and recognize her name. Each requires different capacities which your daughter may or may not have. One way depends on her knowledge of the sounds for each letter in her name. If she has that knowledge -- and has the motor ability to draw the letter forms -- she may with much repetition learn to write and recognize her name.

If she doesn't understand letter-sounds it is possible that she can be taught to write her name in a rote manner if she can repeatedly copy a model or trace a template of her name. Then, if you place a picture of her next to her tracing and keep telling her that both the picture and the written name refer to her, she may eventually relate the written form of her name to herself and recognize it. To further strengthen the relationship between her writing her name and herself, each time she writes her name, say it and help her pat her chest.

If she has trouble with the forming of the letters you might first try having her make the letters in a clay pan with a stylus. The resistance from the clay may make it easier for her to form the letters.

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Why would our nonverbal autistic son be able to speak clearly in complete sentences when very unhappy but not at other times? For example, when he was led away from us to be evaluated by our child study team, the team clearly heard him say "I want Mommy" 2) When he fell and x-rays were necessary his father heard him clearly say "I want to go home". Can you shed any light on this rare speech?
It must be very frustrating for you to know that your son has some speech capacity within him but that it only comes out under great stress...Yes, we have seen this kind of behavior before in children on the autism spectrum... Similar rare speech under emotional stress occurs among aphasic children and adults who have suffered neruolgical damage...

You might recall my comment during the videoconference to the effect that to communicate intentionally (and not just under emotional stress) the child must become consistently more aware of him or herself and the other person. When your child's usual way of being is interrupted (he is led away from his mom, he suffers a very painful injury) the emotional impact may help your chld become more aware of himself and others and may, therefore, allow him to express himself under these conditions while he cannot do so under ordinary circumstances.

This suggests that if we can help children like your son develop greater ongoing awareness of himself in relation to others then he might well reach a point where he can communicate without first having to be emotionally stressed.

The Miller Method includes a variety of strategies -- such as the Elevated Square, "rough and tumble" activity, narration of the child's behavior, setting-up"Can Do!" Picture Boards -- that are designed to help the special child build the better defined self-other relationships which favor spontaneous communication.

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Do you ever use swings in your method? Do you know of any research done on the effectiveness of swinging for autism?
Swings and swinging used in a certain way are definitely part of the Miller Method. When swings are used we recommend that the teacher, therapist or parent push the swing whilce standing in front of the child so that eye contact is maintained. Then, each time the child swings close the adult says, "I'm going to touch your nose, (hand, toe, face, etc.) while observing to see whether or not the child is beginning to anticipate the contact. In this way, swinging contributes to the child's body awareness and awareness of the other.

We also recommend pushing the swing in such a way that it makes different trajectories which provide the child with a varied body experience. Then, unexpectedly, we recommend interrupting the swinging (holding the swing) to determine if the child can in some way indicate a need for the swinging to continue.

Swinging the child in a blanket or parachute is also part of the "rough and tumble" activity (carefully adjusted to each child's sensitivities) we recommend prior to involving the child in more structured activity. Our clinical experience is that the experience of swinging helps "ground" the child but I am not aware of specific research related to the effect of swinging per se.

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GENERAL QUESTIONS


What is Cognitive and language development? What are the different ways in which this affects the children?
Thank you for your interest in the Miller Method. Most of the children we serve have problems being with people and with the ability to use language the way typical children do. Many -- but not all -- have trouble solving problems such as learning to use a chair to get something they want on a shelf out of reach. The term cognitive development refers to where a child is in his or her capacity to solve such problems and others more complicated. The work we do at the Language and Cognitive Development Center of Boston is designed to help children both learn to solve these and more complicated everyday problems and to learn to use language to understand others and to communicate what their needs are to them....At the earliest level, a child might simply pull someone by the hand to get what they want. With language and cognitive development they can communicate their wishes through manual signs and spoken words without hand-pulling.
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If a parent called me and stated that the doctor said that her child has "spectrum disorder," what is it?
If the doctor is referring to "autism spectrum disorder" he is referring to a developmental condition -- involving the central nervous system -- that affects about 1 in 1000 children (mostly boys). The condition shows itself with difficulties establishing human relationships, in delayed or disordered language, difficulty with transitions as well as "self stimulating" behaviors (flapping, twiddling of fingers, rocking, toe walking, etc.). The condition is treated most effectively when begun as early as possible. The Language and Cognitive Development Center of Boston -- using the Miller Method -- specializes in helping these children.
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There are no Miller Method programs where I live in British Columbia. Is there any way you can guide me in using your approach so that I can help my 5-year old autistic son?
Yes. We are currently working with a number of families who live far from our Center through one of the following modalities:

1. Videoconferencing... This allows senior staff at the Language and Cognitive Development Center (LCDC) in Boston to see, hear, answer questions and guide the work done with a special child hundreds or even thousands of miles away.

2. Phone consultation... This method supplemented by videotapes of work being done with a special child and sent to LCDC for review and recommendations is also effective.

3. Internet consultation... This newest method allows a regular exchange of questions and answers between parent and senior staff in a private Interactive Chat Room on the Center's website

If you are interested in any of these methods contact Drs. Arnold Miller or Paul Callahan at 1-800-218-5232.

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How is language development affected by autism?
Excellent question. Language development is affected by autism in several important ways: One, concerns the "word deafness" often found among children on the spectrum. This means that while there is nothing wrong with the children's hearing, they often have great difficulty deriving meaning from spoken words directed toward them. Another area in which communication is affected has to do with their uncertain differentiation of their own bodies from those of others. Without such body-other awareness they have difficulty spontaneously initiating communication. This poor self-other separation is also related to echolalia -- the tendency to repeat whatever is said to them as well as confusion between the use of the terms "I" and "you."

The Miller Method has developed interventions -- involving pairing spoken words with directed body action and gesture -- to cope with "word deafness." The Method also introduces strategies to enhance self-other awareness.

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I read an article by Arnold and Eileen Eller-Miller that Temple Grandin referenced regarding the use of a visualized reading method. Is this method still in use? Is it suitable for reading instruction with a student with autism who has limited expressive but good receptive language?
The Symbol Accentuation (SA) Reading Program which my wife and I developed is still very much in use. It is distributed by Cognitive Designs, Inc. (www.cognitivedesigns.com) and has been used effectively with special children and particularly with those children on the autism spectrum such as your student. In addition to developing reading and writing capacity the program has consistently helped such children with their expressive language.
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