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IF YOU
NEVER START
By Ellen Notbohm
As published in Autism Asperger’s Digest,
November-December 2005
“If you
never start, you’ll never have to worry about stopping.”
That’s my parents, talking to the teenage me about smoking.
“If you
never start, you’ll never have to worry about stopping.”
That’s my kids’ first pediatrician, talking to me about
spanking. “Once you start, where do you stop?” he adds
ominously.
“If you
never start, you’ll never have to worry about stopping.”
That’s me, endlessly explaining to people why I never go to
Starbucks.
You can
see that this adage is at work in my life. But it’s not
always a conscious choice. Sometimes it is intuitive. It is
the reason we never had Nintendo, Gameboy, Play Station or
any other video game system in our home. There was no actual
list in my head of reasons why we shouldn’t let our boys
indulge in this very common contemporary pastime. I just let
inertia do its job – we didn’t have one and if we never got
one we could just bypass all the fights about which games
were OK, how much time they could spend on it, was it
interfering with homework, and of course the expense of the
never-ending demand for new games and upgraded equipment. To
be honest, raising two boys with non-standard needs
constantly taxed my stamina to the outer limits and “one
less thing on the plate” was frequently an appealing
option.
Some
years later our original pediatrician had retired and we
were getting to know a new doctor. He really got my
attention with his reaction to an offhand comment I made
about not having any video games in the house.
“That is
probably the single most important parenting decision you
ever made for these kids.”
Wow. I
didn’t know him well enough then to know if hyperbole was
his style or if this statement was sincere in its incredible
weightiness. The most important parenting decision I ever
made? More important than moving to a new home to get them
into better schools? More important than not allowing
smoking in our home? Double wow. At the time, I ended up
merely accepting it as a nice compliment. But over the years
my mind would wander back to it: “....most important
parenting decision you ever made for these kids.”
Seven
years down the line, it finally occurred to me to ask him
what exactly he meant, especially the qualifier, “for
these kids.” Did he in fact even remember saying it to
me?
I
can well believe I said that, came the answer. And I would
stand by it. And here is why:
Video games – all video games, not just the violent ones -
magnify the issues of autism and ADHD.
In that
one sentence, he made me see video games in all their
unvarnished glory: immersive, addictive, over-stimulating,
socially isolating, sedentary, non- productive, unrealistic
language vacuums that frequently reinforce and reward
socially unacceptable behavior.
Those are
all ugly, compelling arguments against video games, but the
bottom line is much more subtle, even insidious, and it is
this: No parent or teacher, says my doctor, can compete
with the sheer pace of a video game. Real life simply does
not and cannot move that quickly, reward that quickly,
wipe-out-and-start-over that quickly. The artificial
expectation it sets up for the child is insurmountable. It’s
never enough. By contrast, life in “real time,” at the speed
of real life, is boring. The child, already over-stimulated,
seeks even more stimulation. The child who is already hyper
becomes yet more hyper.
If your
child has autism, it’s rather breathtaking to confront just
how thoroughly and actively video games work against the
very challenges we are trying to surmount. Let’s go through
the list.
LIMITED, UNBALANCED SENSORY INVOLVEMENT
Video games overstimulate the visual and auditory senses,
while offering no involvement or development of the other
five senses. The drum-like repetitive action and artificial
sound encourages perseveration.
Have you
heard the argument justifying video games as being good for
hand-eye coordination? There are about a jillion activities
that do so much more constructively: drawing, puzzles,
blocks, Legos, dressing dolls, digging dirt, Nerf sports,
kitchen pursuits. These activities can be just as engrossing
as video games. When my kids were little, they would beg to
play “water cups.” They entertained themselves for as much
as three hours at a time with a trickle of water from the
sink or outdoor hose. They would pour back and forth between
all sorts of containers, mix it with whatever was close by
(dirt, paper napkins, leaves), sing, add shaving cream or
food coloring, get their clothes and hair wet to see how it
felt. Visiting cousins and friends were just as intrigued,
although one was incredulous: “My mother would never let me
do this - I’d get dirty!” I put her in a swimsuit, assured
her that she would leave as clean as she came – it would be
our “dirt-y” little secret. Once she got started, I
literally could not tear her away, even when Dad showed up.
INACTIVITY
“Get up offa that thing!” shouts James Brown’s 30-year-old
song. You can’t turn your head and sneeze anymore without
confronting alarming information about obesity and other
organic diseases that are escalating sharply in today’s
children who aren’t active enough. But there’s more: a
growing body of evidence that suggests cognitive learning is
directly related to physical activity. Schools that
incorporate physical activity programs see positive effects
that include increased concentration, improved math, reading
and writing scores and fewer disruptive behaviors. In my own
life, I was astonished to see Bryce make marked leaps in
reading, math and general cognition immediately after
learning to swim, and later, to ride a bike. I am 200%
convinced of this link, but I also know that finding
physical outlets that our ASD kids can wholeheartedly enjoy
can take more searching, planning and facilitating that it
does for NT kids. Actually, that’s another whole column in a
future issue. For now, start thinking about non-team sports
and non-competitive active pursuits, and be sure to read
Sarah Spella’s Ask the Experts column, about adapted
physical education, in this issue.
OBSCURES THE LINE BETWEEN FANTASY AND REALITY
Distinguishing between fantasy and reality requires the
ability to engage in perspective-taking, something children
with autism are notoriously lacking. For many of our kids,
that inability has ominous implications as applied to
Ninja-chopping, motorcycle-crashing, machine gun-blasting
video games – or any other “harmless” fantasy portrayal. Do
you dare imagine what Wyle E. Coyote REALLY looked after he
went over that cliff with a cache of dynamite?
Last year
Bryce’s class had an assignment wherein each student wrote
and presented a short speech “in character” as a famous
ancient Greek. Bryce chose Alexander the Great (“the only
name on the list I could pronounce,” he said, only
half-joking.). His classmate Michael (also on the spectrum)
chose Zeus. When I commented that Zeus was a mythical person
as opposed to Alexander who was quite real, Bryce’s startled
reaction was: “What? Does Michael know this?” I met up with
Michael’s mother at school shortly thereafter and relayed
the question to her. Her reaction: eyes rolling a bit sadly
as she replied, “Does Michael ever know the difference
between fantasy and real?”
It’s
something to consider if your child suffers from nightmares
– and can’t quite tell you why. Temple Grandin has stated
frequently that she avoids movies with graphic depictions of
violence because, as a visual thinker, the images sear
permanently into her brain and she cannot get rid of them.
REWARDS UNACCEPTABLE, ILLEGAL BEHAVIOR
Nor is it realistic to expect the child with autism to
understand that the violent or destructive action in a video
game is “for entertainment purposes only.” This is the part
I find most scary. Games whose object is to blow up, blow
away or lop body parts off of opponents reward successful
violent behavior. The child receives instant positive
reinforcement for killing and maiming. Worse, as opposed to
TV, he is participating in the violent activity
rather than merely watching it. Worst case scenario: these
are behaviors that, if emulated, can later land him in jail.
The nuances of law enforcement are going to be enough of a
challenge for him without the added handicap of pondering
helplessly why it was OK in his favorite game but not OK on
the actual corner of 5th and Elm.
SOCIAL
SKILLS VOID
Think of all the elements that go into healthy social
development. Ask yourself if video games fulfill any of
these for your child: engaging in positive interpersonal
interactions, building a sense of worth and self-definition,
expressing himself through creative thinking and activities,
being a meaningful participant in a group. Are video games
helping him learn to impose the self-discipline needed to
structure his time, set reasonable limits, prioritize tasks?
Are they helping him learn to distinguish and choose
gracefully between wanna-do’s and hafta-do’s? Or between
privileges and rights?
LANGUAGE-DEVELOPMENT BLACK HOLE
Language development is among the most urgent of issues for
many, many children with autism, and in this regard, there
are few worse friends than the video game. Played in
isolation, there is no useful language happening at all.
Even in parallel play with a friend or sibling, attention is
fixated on the screen and whatever minimal verbal exchange
that takes place generally relates only to what is happening
on the screen.
A ROLE
IN REGRESSION?
Does your child demonstrate social or cognitive regression
following summers and extended school breaks? If he’s
whiling that time away in front of a screen, it might be
useful to question the role of video games. All skill
development, whether it’s reading, making conversation,
taking turns at games, hitting a tennis ball, baking
brownies or tracking down the evil Super Mario double, takes
practice. Extended time off from school shouldn’t be
time to abandon social and cognitive learning. Do the math:
a child who is in school 6.5 hours a day, 175 days a year is
spending only 22% of his 16 waking hours/365 days in that
school. The other 78% of his time, the instruction is up to
you.
A child’s
job is to explore the world. For our kids with autism, that
exploration may be a little more tenuous, a little more
treacherous. But explore they must and that means touching,
talking, tasting and trekking, discovering. For all
time before the 20th century, this happened
without the aid of a video screen. Long before my doctor had
anything to say about it, the great writer Johann Wolfgang
von Goethe did: “Talent develops in solitude, character in
the full current of human life.”
© 2006
Ellen Notbohm
Ellen Notbohm is author of Ten
Things Every Child with Autism Wishes You Knew, a
ForeWord 2005 Book of the Year Honorable Mention winner and
recipient of iParenting’s 2005 Media Award, and Ten
Things Your Student with Autism Wishes You Knew, a 2006
iParenting Media Award recipient. She is co-author of
1001 Great Ideas for Teaching and Raising Children with
Autism Spectrum Disorders, winner of Learning
Magazine’s 2006 Teacher’s Choice Award, and a columnist for
Autism Asperger’s Digest and Children’s Voice. For article
reprint permission, to learn more or to contact Ellen,
please visit
www.ellennotbohm.com |
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TEN
THINGS EVERY CHILD WITH AUTISM
WISHES YOU KNEW
by Ellen Notbohm
Some days it
seems the only predictable thing about it is the
unpredictability. The only consistent attribute – the
inconsistency. There is little argument on any level but
that autism is baffling, even to those who spend their lives
around it. The child who lives with autism may look “normal”
but his behavior can be perplexing and downright difficult.
Autism was
once thought an “incurable” disorder, but that notion is
crumbling in the face knowledge and understanding that is
increasing even as you read this. Every day, individuals
with autism are showing us that they can overcome,
compensate for and otherwise manage many of autism’s most
challenging characteristics. Equipping those around our
children with simple understanding of autism’s most basic
elements has a tremendous impact on their ability to journey
towards productive, independent adulthood.
Autism is an
extremely complex disorder but for purposes of this one
article, we can distill its myriad characteristics into four
fundamental areas: sensory processing challenges,
speech/language delays and impairments, the elusive social
interaction skills and whole child/self-esteem issues. And
though these four elements may be common to many children,
keep front-of-mind the fact that autism is a spectrum
disorder: no two (or ten or twenty) children with autism
will be completely alike. Every child will be at a different
point on the spectrum. And, just as importantly – every
parent, teacher and caregiver will be at a different point
on the spectrum. Child or adult, each will have a unique set
of needs.
Here are ten
things every child with autism wishes you knew:
1. I am first and foremost a child. I have autism. I am not
primarily “autistic.” My autism is only one aspect of my
total character. It does not define me as a person. Are you
a person with thoughts, feelings and many talents, or are
you just fat (overweight), myopic (wear glasses) or klutzy
(uncoordinated, not good at sports)? Those may be things
that I see first when I meet you, but they are not
necessarily what you are all about.
As an adult, you have some control over
how you define yourself. If you want to single out a single
characteristic, you can make that known. As a child, I am
still unfolding. Neither you nor I yet know what I may be
capable of. Defining me by one characteristic runs the
danger of setting up an expectation that may be too low. And
if I get a sense that you don’t think I “can do it,” my
natural response will be: Why try?
2. My sensory perceptions are disordered.
Sensory integration may be the most difficult aspect of
autism to understand, but it is arguably the most critical.
It his means that the ordinary sights, sounds, smells,
tastes and touches of everyday that you may not even notice
can be downright painful for me. The very environment in
which I have to live often seems hostile. I may appear
withdrawn or belligerent to you but I am really just trying
to defend myself. Here is why a “simple” trip to the grocery
store may be hell for me:
My hearing may be hyper-acute. Dozens of people are talking
at once. The loudspeaker booms today’s special. Musak whines
from the sound system. Cash registers beep and cough, a
coffee grinder is chugging. The meat cutter screeches,
babies wail, carts creak, the fluorescent lighting hums. My
brain can’t filter all the input and I’m in overload!
My sense of smell may be highly sensitive. The fish at the
meat counter isn’t quite fresh, the guy standing next to us
hasn’t showered today, the deli is handing out sausage
samples, the baby in line ahead of us has a poopy diaper,
they’re mopping up pickles on aisle 3 with ammonia….I can’t
sort it all out. I am dangerously nauseated.
Because I am visually oriented (see more on this below),
this may be my first sense to become overstimulated. The
fluorescent light is not only too bright, it buzzes and
hums. The room seems to pulsate and it hurts my eyes. The
pulsating light bounces off everything and distorts what I
am seeing – the space seems to be constantly changing.
There’s glare from windows, too many items for me to be able
to focus (I may compensate with "tunnel vision"), moving
fans on the ceiling, so many bodies in constant motion. All
this affects my vestibular and proprioceptive senses, and
now I can’t even tell where my body is in space.
3. Please remember to distinguish between won’t (I
choose not to) and can’t (I am not able to). Receptive and expressive language and
vocabulary can be major challenges for me. It isn’t that I
don’t listen to instructions. It’s that I can’t understand
you. When you call to me from across the room, this is what
I hear:
“*&^%$#@,
Billy. #$%^*&^%$&*………”
Instead, come speak directly to me in plain words: “Please
put your book in your desk, Billy. It’s time to go to
lunch.” This tells me what you want me to do and what is
going to happen next. Now it is much easier for me to
comply.
4. I am a concrete thinker. This means I interpret language
very literally. It’s very confusing for me when you
say, “Hold your horses, cowboy!” when what you really mean
is “Please stop running.” Don’t tell me something is a
“piece of cake” when there is no dessert in sight and what
you really mean is “this will be easy for you to do.” When
you say “It’s pouring cats and dogs,” I see pets coming out
of a pitcher. Please just tell me “It’s raining very hard.”
Idioms, puns, nuances, double entendres, inference,
metaphors, allusions and sarcasm are lost on me.
5. Please be patient with my limited vocabulary.
It’s hard for me to tell you what I need when I don’t know
the words to describe my feelings. I may be hungry,
frustrated, frightened or confused but right now those words
are beyond my ability to express. Be alert for body
language, withdrawal, agitation or other signs that
something is wrong.
Or, there’s a flip side to this: I may sound like a “little
professor” or movie star, rattling off words or whole
scripts well beyond my developmental age. These are messages
I have memorized from the world around me to compensate for
my language deficits because I know I am expected to respond
when spoken to. They may come from books, TV, the speech of
other people. It is called “echolalia.” I don’t necessarily
understand the context or the terminology I’m using. I just
know that it gets me off the hook for coming up with a
reply.
6. Because
language is so difficult for me, I am very visually
oriented. Please show me how to do something rather than
just telling me. And please be prepared to show me many
times. Lots of consistent repetition helps me learn.
A visual schedule is extremely helpful as I move through my
day. Like your day-timer, it relieves me of the stress of
having to remember what comes next, makes for smooth
transition between activities, helps me manage my time and
meet your expectations. Here’s a great website for learning
more about visual schedules:
www.cesa7.k12.wi.us/sped/autism/structure/str11.htm.
I won’t lose the need for a visual schedule as I get older,
but my “level of representation” may change. Before I can
read, I need a visual schedule with photographs or simple
drawings. As I get older, a combination of words and
pictures may work, and later still, just words.
7. Please focus and build on what I can do rather than what
I can’t do. Like any other human, I can’t learn in an
environment where I’m constantly made to feel that I’m not
good enough and that I need “fixing.” Trying anything new
when I am almost sure to be met with criticism, however
“constructive,” becomes something to be avoided. Look for
my strengths and you will find them. There is more than one
“right” way to do most things.
8. Please help me with social interactions.
It may look like I don’t want to play with the other kids on
the playground, but sometimes it’s just that I simply do not
know how to start a conversation or enter a play situation.
If you can encourage other children to invite me to join
them at kickball or shooting baskets, it may be that I’m
delighted to be included.
I do best in structured play activities that have a clear
beginning and end. I don’t know how to “read” facial
expressions, body language or the emotions of others, so I
appreciate ongoing coaching in proper social responses. For
example, if I laugh when Emily falls off the slide, it’s not
that I think it’s funny. It’s that I don’t know the proper
response. Teach me to say “Are you OK?”
9. Try to identify what triggers my meltdowns.
Meltdowns, blow-ups, tantrums or whatever you want to call
them are even more horrid for me than they are for you. They
occur because one or more of my senses has gone into
overload. If you can figure out why my meltdowns occur, they
can be prevented. Keep a log noting times, settings, people,
activities. A pattern may emerge.
Try to remember that all behavior is a form of
communication. It tells you, when my words cannot, how I
perceive something that is happening in my environment.
Parents, keep in mind as well: persistent behavior may have
an underlying medical cause. Food allergies and
sensitivities, sleep disorders and gastrointestinal problems
can all have profound effects on behavior.
10. If you are a family member, please love me
unconditionally.
Banish thoughts like, “If he would just……” and “Why can’t
she…..” You did not fulfill every last expectation your
parents had for you and you wouldn’t like being constantly
reminded of it. I did not choose to have autism. But
remember that it is happening to me, not you. Without your
support, my chances of successful, self-reliant adulthood
are slim. With your support and guidance, the possibilities
are broader than you might think. I promise you – I am worth
it.
And finally, three words: Patience. Patience. Patience.
Work to view my autism as a different ability rather than a
disability. Look past what you may see as limitations and
see the gifts autism has given me. It may be true that I’m
not good at eye contact or conversation, but have you
noticed that I don’t lie, cheat at games, tattle on my
classmates or pass judgment on other people? Also true that
I probably won’t be the next Michael Jordan. But with my
attention to fine detail and capacity for extraordinary
focus, I might be the next Einstein. Or Mozart. Or Van
Gogh.
They had autism too.
The answer to Alzheimer’s, the enigma of extraterrestrial
life -- what future achievements from today’s children with
autism, children like me, lie ahead?
All that I might become won’t happen
without you as my foundation. Think through some of those
societal ‘rules’ and if they don’t make sense for me, let
them go. Be my advocate, be my friend, and we’ll see just
how far I can go.
© 2005 Ellen Notbohm
Ellen Notbohm is author of Ten
Things Every Child with Autism Wishes You Knew, a
ForeWord 2005 Book of the Year Honorable Mention winner and
recipient of iParenting’s 2005 Media Award, and Ten
Things Your Student with Autism Wishes You Knew, a 2006
iParenting Media Award recipient. She is co-author of
1001 Great Ideas for Teaching and Raising Children with
Autism Spectrum Disorders, winner of Learning
Magazine’s 2006 Teacher’s Choice Award, and a columnist for
Autism Asperger’s Digest and Children’s Voice. For article
reprint permission, to learn more or to contact Ellen,
please visit
www.ellennotbohm.com |
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About
Edward C. Fenske,
M.A.T. Ed.S |
Preparing a Child with Autism for the
Arrival of a New Sibling
Edward C. Fenske, M.A.T., Ed.S.
All family members must make adjustments
when a newborn child arrives in their home. Standard
routines for meals and bedtime may be disrupted and
older children may experience difficulty in coping with
less parental attention. Children with autism are often
extremely resistant to changes in their routines and may
present other unique challenges to parents when the baby
arrives. A proactive approach is best. Many problems can
be anticipated and minimized through early preparation. |
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An
amazing array of new furniture and equipment appears in the
home when a new baby arrives. Some children with autism may
find these new objects to be of interest. Because parents
will have much more time to teach new skills before the baby
is born, it is advisable to furnish the baby’s room and
purchase equipment early. Parents should set clear and
consistent limits about which items their child with autism
can touch and under what circumstances. We have encouraged
parents to purchase a life-like doll and rehearse new
routines such as feeding, changing, and bathing the baby. A
child with autism can have a role in some of these
activities. For example, he could assist mom or dad by
following directions such as: “Bring me a clean diaper,”
“Put this bottle in the sink,” or “Hang up this towel
please.” Initially parents may have to prompt their child to
follow these new directions. Parents should have their child
practice these directions frequently and gradually fade
prompts as she becomes more proficient. As prompts are being
faded, reward your child when he makes the correct response
with minimal prompting. Eventually reserve rewards for
unprompted responses. Strategies for fading prompts can be
found in MacDuff, Krantz, and McClannahan (2001). Daily
practices will help your child master these directions
before the baby arrives, when parents have less time for
teaching, prompting, and rewarding.
Some
children with autism become upset when they hear loud
noises. Therefore it is important to teach a child with
autism strategies for coping with the inevitable episodes of
crying that will occur when the baby arrives. We have
tape-recorded crying sounds to use when teaching children
appropriate ways to respond. One technique is to teach the
child with autism to go to another room, put on headphones
and listen to music whenever the baby cries. The parent
positions the tape player close to the life-like doll,
presses the play button, and immediately prompts the child
to obtain the headphones, put them on, and start the music.
Rewards (e.g., bite-sized snacks and praise) are delivered
during teaching to shape unprompted responses and
appropriate behavior. Rewards should not be delivered if the
child with autism becomes upset because you will be
rewarding him for crying. At first it may be necessary to
play the tape at a very low volume or for a very brief
period of time in order to increase the likelihood of
success (i.e., the child does not become upset when he hears
crying sounds). Gradually increase the volume and duration
of the recording. Frequent rehearsals promote faster skill
acquisition and also help desensitize the child to the sound
of crying.
The
demands of caring for a newborn child mean less direct
parental supervision for a child with autism, and without
supervision she may display high rates of stereotypic
behavior. While parents may be able to enlist the support of
family members or hire a child-care provider, constant
one-to-one supervision promotes prompt dependence (e.g., he
doesn’t play with his toys unless an adult gives him a
direction). Children who have learned to independently
initiate play and leisure activities are not only better
prepared to adjust to the addition of a new sibling, but are
developing skills that increase their social competency and
promote positive treatment outcomes. Photographic and
written activity schedules have been found to be effective
in promoting independent performances and appropriate
engagement (MacDuff, Krantz, and McClannahan, 1993). When
teaching children to follow an activity schedule, adults
employ and systematically fade manual prompts. After all
prompts have been faded, photographs or words cue the child
to initiate the specified activities. Schedules include not
only isolate activities, but also cue children to initiate
social interaction (McClannahan and Krantz, 1999). A child
who becomes a good schedule follower selects and completes a
variety of independent and interactive activities. For
example, he might first complete a PLAYFUL PATTERNS® design
and then ask a parent to play ZINGO!® (Discovery Toys,
2006).
The
addition of a newborn brings many changes to family
routines. However early planning and preparation enable
parents to take a proactive approach and teach skills that
help their child with autism make a successful adjustment.
References
MacDuff,
G.S., Krantz, P.J., & McClannahan, L.E. (2001). Prompts and
prompt-fading strategies for people with autism. In C.
Maurice, G. Green, & R.M. Foxx (Eds.), Making a Difference :
Behavioral intervention for autism (pp. 37-50), Austin, TX:
Pro-ed.
MacDuff,
G.S., Krantz, P.J., & McClannahan, L.E. (1993). Teaching
children with autism to use photographic activity schedules:
Maintenance and generalization of complex response chains.
Journal of Applied Behavior Analysis, 26, 89-95.
McClannahan, L.E., & Krantz, P.J. (1999). Activity Schedules
for children with autism: Teaching independent behavior.
Bethesda, MD: Woodbine House. |
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Dealing with the Diagnosis of Autism
by Debbie Lignell, MA, LMFT
The hopes and dreams we
have for our children and ourselves as parents often
begin long before we learn we are going to be parents.
For some it begins in early childhood rocking and loving
that first baby doll. For others, it happens as they
become older siblings and learn to care for their
younger counterparts. Still for others, it happens when
they are touched by a moment observed between a parent
and child. Whenever it happens, it is important to
realize how powerful those dreams and fantasies are and
how much they impact our lives, especially when our
reality and the dreams we’ve carried do not match.
As a parent, it is
devastating to learn that your child is not developing
typically. It can be plainly obvious something is wrong
or it can be more subtle and a parent has a strong “gut”
feeling that something isn’t right. Receiving a
diagnosis of autism or Autistic Spectrum Disorder is
often the jolt that begins a process similar to grief
and loss for parents, which they must learn to address
so they can find a path to new versions of their hopes
and dreams.
The parents and
families I have worked with have taught me much about
this process. While their children continue to live and
learn to function to the best of their abilities,
parents may still face the loss of their dreams of how
being a parent would be and what their child may be able
to accomplish. Parents must grieve that loss to be able
to move forward and be truly present with their
child. Often parents need support to through these
steps. Being familiar with the grief cycle can help all
of us empathize and understand where a parent may be
coming from on any particular day and give them the help
they need.
These stages of the
grief cycle can happen in any order and can overlap or
repeat, just like when we deal with other types of
emotions. The following describe what a parent who is
adjusting to a child with disabilities often experiences
(D.Cansler, G. Martin, & M. Valand. Working with
Families. 1975).
Denial:
A parent may experience shock, not fully understanding
what this means for them or their child. They may flatly
disregard the diagnosis entirely searching for many more
opinions and they may act as if nothing is wrong at all.
They may have a sense of this is all just “un-real.”
Intellectual
Awareness: At this stage, a
parent may feel anger, guilt, depression, overwhelming
grief and sorrow, disappointment, bitterness, shame or
blame others. It is this stage that is most often
“re-visited.”
Intellectual
and Emotional Adjustment (Acceptance):
Here a parent begins to organize time and energy
constructively and begins to learn and create new goals
and realistic expectations for their child. They begin
to learn to advocate for their child and their family
and cooperates with those working with their child in
the best treatment plan possible.
Receiving a diagnosis
of autism impacts a family immediately and brings many
stresses. Parents must readjust their expectations of
their child, manage financial issues, deal with how the
news affects their relationships, cope with how siblings
may be feeling and deal with a variety of healthcare
professionals and systems. Parents have difficulties
even dealing with the everyday aspects of life that we
all take for granted, such as taking their child out to
the store and how to answer questions when they arise.
Many factors influence how a family will go through this
period of adjustment. Some of these being the severity
of the autism, the support system the family has within
the family and the support systems that exist beyond the
family.
No two people handle
life's struggles in exactly the same way, and when
working with parents who are affected by autism, it can
sometimes be confusing and takes patience and skill to
figure out how to help. You may work with them one day
talking openly and frankly about what their child is
able to do and how you might adapt a toy or game to work
for them. The next time you see them, they may
be discouraged, expressing that their child will never
be able to use that toy or game effectively. On the flip
side, they may present it as if no modifications are
necessary for their child to use a toy or game.
Regardless of the frustrations they face, parents of a
child with autism know that it is important to celebrate
each success and that day to day progress can be made
with the help of intervention programs, love, attention,
and of course fantastic toys to make learning fun and to
keep their child focused on building skills.
We can continue to
support parents by gently reminding them of constructive
points from previous conversations, offer them support
and understanding of the process they are going through,
and sometimes we can be the “holders” of hope. We can
hope for more of an understanding of autism. We can hope
for a cure. We can hope for a better tomorrow. We can
hope for more good moments than hard ones, and in that
hope lies possibility.
Because there is such a
wide variance of abilities within the diagnosis of
autism, especially when you include the many disorders
on the autistic spectrum, no two cases will ever be the
same. Many children with autism build skills in some,
possibly ALL areas of development and that allows them
to function for short and even long periods alongside
their peers. Helping parents achieve a balance of
realistic expectations, and holding onto hope is
challenging, but it is a big part in creating a
positive environment that will benefit their child.
One parent I had the
honor of working with has allowed me to share her story
because it summarizes this perfectly. She said that she
and her husband would often let their young son sleep
with them because when he was asleep, and they were next
to him sharing that close moment, they could see his
potential without barriers. They could give themselves
that time to bathe in the hope that something in his
future would allow him to come out of the inner world he
was trapped in. She shared that for her, the daytime
hours didn’t allow the luxury of what “might” be because
they were so filled with the demands of what “is,” but
the nighttime was different. She added, in sleep, there
is no difference between a child with autism and child
who doesn’t have it. |
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About
Edward C. Fenske, M.A.T. Ed.S |
Helping Your Child with Autism Acquire and Use
Language
Skills
Impairment in the development of language and communication
skills is a defining characteristic of autism spectrum
disorder (Diagnostic and Statistical Manual of Mental
Disorders American Psychiatric Association, 2000) and
parents are very concerned about their child’s
acquisition of language skills. The very title of the
book Let Me Hear Your Voice (Maurice, 1993)
expresses one parent’s anguish over her child’s
inability to talk. The first scientifically validated
procedure for teaching language skills to children with
autism occurred in a structured therapeutic setting
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(Lovaas,
1977). However more recent research has identified
teaching strategies that are employed in natural
settings and therefore easily used by parents during
typical daily activities.
Incidental teaching, developed by Hart and Risley (1968),
is a procedure that helps children learn to initiate
requests for items of interest. Research on the use of
incidental teaching for language instruction of children
with autism demonstrates that this procedure promotes
generalization and spontaneous use of new skills
(McGee, Krantz, & McClannahan, 1985).
Detailed descriptions of the use of incidental teaching are
available in other sources (Hart & Risley, 1982; Fenske,
Krantz, & McClannahan, 2001). This article will provide
the reader with an overview of incidental teaching and a
few examples of ways to use this procedure for language
instruction. The components of incidental teaching are:
(a) obtaining materials of interest to the child and
arranging them in ways that promote child initiations,
(b) waiting for the child to initiate for an item of
interest, (c) requesting or modeling a request with more
elaborate language, and (d) providing the child with the
item of interest.
Parents can increase their child’s interest in materials by
selecting or purchasing favorite snacks, toys, or
activities and placing them where they are visible but
not accessible by the child. For example, place the
Marbleworks®
Deluxe Set on a high shelf that is beyond your child’s
reach.
The next step is often the hardest. You have to wait for
your child to make an initiation. Don’t ask, “Do you
want Marbleworks?” Asking questions or giving directions
will not help your child learn to spontaneously make
requests. The way in which your child initiates will
depend upon his current skills. Non-verbal children may
initiate by reaching. Children with more verbal skills
might request an item with a word or phrase (e.g.,
“Marbles” or “Play marbles”). You can encourage
initiations by glancing at or manipulating the toy, but
afterwards wait until your child initiates for it.
Your child indicates his interest in an object by making a
non-verbal or verbal initiation, and now you have an
opportunity to teach him to use language or to use more
language. Consider your child’s current language skills
when requesting elaborated language. If the initiation
was non-verbal, request a sound (e.g., Say, “/m/”). If
he initiated with a single word, ask him to say a phrase
(e.g., Say “play marbles” or “marbles please”). Some
children may already have functional language skills in
their repertoires, although they seldom use these
skills. In this case, you may be able to request
elaborated language by simply asking, “What do you
want?”
After he provides the target language response, give him
the item of interest. In incidental teaching the reward
is the object for which the child initiated. This
procedure teaches children the function of
language. They learn that language is important because
it affects people and events in their daily life. If you
are thirsty and say “juice” you probably will get
something to drink. One word of caution, if your child
initiates by having a tantrum, do not give him the item
of interest. He may learn to communicate by displaying
problem behavior. |
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References
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