Zachary's Tale - A Journey Into Sensory Disfunction

The time on the clock says 9:30; I look down atthe house. All those noises crowding into your
my sleeping little boy, whom I have just quietlymind would be making it nearly impossible for you
rocked to sleep. He is still latched on somewhat,to concentrate on the most simple of tasks, from
comfort nursing. As we rock I stare down at himplaying to learning. Being unable to communicate
and wonder what his future might hold.to let anyone know that any of them is even
Zachary is my 27-½ month old son, andbothering you.
has been diagnosed (I hate that word; to me itMaybe if you could crave putting everything into
some how implies that there's something wrongyour mouth, because you need that form of
that medicine could fix) with Sensory Integrationstimulation. If you really had NO way of
Dysfunction and delayed speech, as well as havingcommunicating except for grunting, or crying.
some feeding or eating issues. These diagnosesYou'd have no way to let the world around you
were made about 6 months ago with a team ofknow anything about what was going on in your
qualified therapists and specialists.head, your thoughts or feelings. No way to show
Life with and for Zachary is not at all like the life Ithat you're feeling totally lost.
had envisioned for him. Of course as a new mom,Maybe if you picked incessantly on yourself, your
you have all the hopes, expectations and desires"boo-boos," and fingers until they bleed, without
that every new mom has. Also, with having aneven feeling the pain of what you're doing. Or if
older child, my work in a preschool and being astrangers looked at you, rolling their eyes, or
nanny; I had an idea of what was to come. Ipointing there fingers at you, because you're
thought I knew to expect talking, walking, finegrunting instead of talking or you're hitting yourself
motor skills, eating on queue as well as otherinstead of playing.
things. It all seemed so laid out in some sort ofMaybe if you could not last at a single task longer
master plan, at least it did for all of the kids I hadthan two or three minutes, all the while hating
ever seen before.transitions and screaming, crying and throwing a
Around the time my son turned one I began tofit at every change that had to be made, no
really take notice of little differences in him,matter how small. If you got sick every time you
differences that most first time moms might notgot into the car because of the lack of control. If
have noticed until much later. One thing I noticedyou could climb to very high places and just jump
was his lack of wanting to eat baby foods (heoff, without the fear of being hurt. If going into a
was still nursing for most of his food, and evencrowed place literally freaked you out, for no
today nurses for a good portion of the food heother reason other than all the people. If the idea
takes in). His inability to fall asleep easily (it canof pouring water, or anything onto your head or
take him between 30 minutes to 2 hours to fallinto your face sent you spiraling into a tailspin of
asleep) and his lack of making little baby noisesscreaming and clawing for a breath, because you
(Zachary was never a "babbler" and at 27 monthsbelieved that you were being suffocated.
has JUST started to babble) struck me. Even hisMaybe, if you could live every day, feeling, just
ability to walk was off (he was always bumpinglike this, you could. But I don't, for one second,
into things). He was a SUPER active (almostthink so.
over-active) little boy who craved motion,To look at Zachary, you would think "no problem"
especially in climbing, still does.he's a normal little boy. However, that's not the
At this point, I decided to turn to several closecase, what I've described is just a small piece of
trusted friends, whom all suggested the book,what my little boy goes though EVERY minute of
"The Out of Sync Child". While reading this book,EVERY day. I don't think you could do it, nor do I
on almost on every page, on almost every area Ithink you would want to.
was shaking my head in agreement with justThe therapists he works with now are helping a
about everything that was being said! "YES" IHUGE amount. Zachary is now using some sign
thought, finally something that described "mylanguage to talk to us, is babbling, and is much
child," something that could give me ideas thatmore willing to try foods and other things that
enabled me to help him, and where I could go tomake him "ick-a-fied". It is, however, a very good
get help for him! I had finally found something thatthing that I got him into the program at his young
"made sense". Every aspect of Zachary's lifeage. Research shows that working with a young
seemed to some how make sense; even things Imind is much easier than working with an older
did not think were connected, I learned were!one. Young children are felt to have a "plastic"
Every area touched on within the book seemedbrain, meaning that it can still be rebuilt or
to directly (at least in some part) correlate withchanged. The older a child gets the harder it is to
what Zachary was doing and/or seemed to bechange the behaviors and structure.
feeling. How he was acting or reacting to theOne of the huge battles kids like Zachary face is
world and life around him finally started to makethat they appear so "normal", there are no "tell tail
sense to me!signs" that there is something "amiss" deep within
So, about half way though the book, I called mytheir little brains. So people look at them and think,
state program Early Intervention. We set up a"normal, no issues" then start to think there's
meeting for 5 months later; it seems nothing insomething emotionally wrong with them.
the "system" works fast. On the date of hisIn general terms, Sensory Integration Dysfunction
evaluation, he was formally given the diagnoses ofis basically the inability for the brain to process the
Sensory Integration Dysfunction, with a speechinformation that is brought in though your senses
delay.(whether those senses are internal or external).
For us Zachary's sensory and speech issuesThe dysfunction happens in the central nervous
follow us all day long, every day.system deep within the brain. So basically it's
So could you walk a mile in his shoes?when a "glitch" occurs, and the brain can not
Maybe you could.. That is, if you ever got youranalyze, organize, connect or integrate the
socks on "just right." You may need to havesensory messages it is being sent. Internal or near
them taken on and off five or six times to getsenses would be; vesicular sense (the inner ear)
the seams so they lay "just so" and the tightnesswhich processes information on movement,
around the leg to be "ok." Then you would needgravity and balance, the tactile sense (skin) which
to scream though putting on a fleece or cottonprocesses touch, as well as the proprioceptive
union suit, because you can not communicate tosense (muscles and joints) which process
anyone, what's wrong with this particular outfit.information about the body positions and body
Then, while it's being put on; you pull, yank, cryparts. The external or far senses would be smell,
and even scream (sometimes hitting, if it is extratouch, sight and sound.
painful) until the suit gets on perfectly so theThe end result being that the child (or adult)
seams are "ok" or the tags are not sticking you insuffering from Sensory Dysfunction can not
the back.correctly respond to sensory information, in turn
Maybe you could.. if your mommy would tell youmaking meaningful consistent behavior nearly
three or four times before you change activities,impossible for them. Where a "normal" child just
making sure you heard and understood. Repeatinghas it, the child with a sensory dysfunction has to
herself over and over, because the lights are inwork, and work HARD at achieving it. The child
your eyes, your sister is breathing and talking, orcan have an over sensitivity, under sensitivity or
the fan is on; making it nearly impossible for youboth (which is most often the case.)
to concentrate on what she's saying.Children like my son, who have sensory problems,
Maybe if you understood that the texture, smellare literally fighting an internal fight with
and taste of most foods, would be too much forthemselves every day, only processing half of
you. So much so that meal times will be nearlywhat the world around them has to offer.
impossible for you to cope with. But knowing thatMaybe, you think you have the abilities to walk
you're one of the "lucky ones", your mom is stillaround in my son's shoes..
comfortable with nursing you, so you at leastHowever, I don't think you could walk in those
have a good form of nourishment. Since youshoes..
would nurse anywhere from 4 to 10 times a day.Not because the shoes are too small but because..
Maybe if you heard EVERY little bump, burp, andYou're not special enough.
voice no matter where they came from within