2011年11月30日 星期三

Looking For Sensory Integration For Autism


For many children with autism sensory integration is an important tool. Parents can use sensory integration to enhance some of the skills they want their children to use. We will explore how a parent can locate professionals who are skilled in sensory integration.

Usually an Occupational Therapist (OT) is the person to look for when you are interested in sensory integration for your child with autism. One of the first places to look for someone knowledge about it would be the school system.

Of course you can get services through the school system. I am always looking for inexpensive ways to get the services that children with autism need.

One of the less known ideas is that many school system Occupational Therapists also have a private practice. You may be able to get more hands on this type of therapy in this manner.

Another way to find an Occupational Therapist that can do sensory integration is to look for Hippo therapy or Horse Riding Therapy. This type of therapy is widely considered sensory integration and even children with autism seem to love it. Something about the rhythm of the horse seems to calm our children down.

Do not be scared that your child might be afraid of the horse as the Occupational Therapists have specific training to do this kind of therapy. In my experience the OT was able to go very slowly if needed and still provide activities that helped my child

When looking for sensory integration you can also ask other parents. You may also want to spend time with the OT. Many of the activities an OT uses can be replicated when you are trying to get your child to focus. Of course you want to be taught by the OT exactly what they are doing and why to get the most benefit.




Would you like more free information? Please register here: http://autismonabudget.blogspot.com/2009/12/free-information.html

Mylinda Elliott is the parent of five children. The third of the five has Autism which was diagnosed early on. The fourth of the five children has Aspergers. She is a self taught expert on Autism Spectrum Disorders. Mylinda Elliott has also worked professionally in the disability world for the past fifteen years. She is considered the "Go To" woman for advice or resources on disabilities.





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Autism, Sensory Integration, and Everyone


Sensory integration, explained in a very simple way, is how we understand the events and people in our lives. The way you or I might perceive other people or events can be quite different than the way a child with Autism feels them. Basically our minds and our bodies take in the information we get from our senses. Everything we see, hear, smell, and taste goes through a process. Part of the process is a designation of what order or importance all of these thing are to a person,

We are receiving and feeling all of this information at once. Our brain is the system that takes all of this information and changes it into an order. In a child with Autism this process is quite different. This happens for many different reasons. One of these reasons can be a child with Autism may be hyperactive. The hyperactivity makes it hard for them to slow down and order the information they are receiving.

Another reason may be that the child with Autism is hypo-sensitive. This means the information they are getting is not being ordered because they are not excited enough or curious enough to do it. To further complicate matters the child may be receiving too much information at one time. When this happens the child can become overwhelmed. They could shut down or becoming defensive or aggressive.

No matter how you cut it this sensory integration is an all day everyday event. Sensory integration has many layers to it. No matter how it is perceived it will continue to happen, to everyone. Although shutting down, becoming defensive, and becoming aggressive seem to be strange ways to deal with the issue, it really is not. A typical person deals with sensory integration by walking away, getting angry, and verbally defending themselves.

Typical people are just better at the techniques they employ to walk away, get angry, etc. A child with autism may or may not be able to use the same techniques if they are properly taught how. Proper training is critical to the child who is aggressive or runs.




Would you like more free information? Please register here: http://autismonabudget.blogspot.com/2009/12/free-information.html. Mylinda Elliott is the parent of five children. The third of the five has Autism which was diagnosed early on. The fourth of the five children has Aspergers. She is a self taught expert on Autism Spectrum Disorders. Mylinda Elliott has also worked professionally in the disability world for the past fifteen years. She is considered the "Go To" woman for advice or resources on disabilities.





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2011年11月29日 星期二

Sensory Integration Therapy


Over the years, many studies have demonstrated a link between sensory integration therapy and improving the quality of life for autistic people.

Sensory integration therapy is a valuable tool to teach autistic children how to interact with their environment. One of the main difficulties autistic children face is how they perceive the environment. Oftentimes, their sensory impulses are contradictory to what is expected by society.

Autistic children often have severe difficulty managing their sensory perceptions and a host of seemingly self-destructive behaviors or actions that are perceived to be senseless is the result. Autistic people sometimes cannot perceive their own physicality and must resort to these behaviors to "feel" something. For instance, some autistic children may bang their head against a wall or spin around in circles. Others have been known to self harm or crash into objects. These behaviors are the direct result of sensory integration impairment.

The process of sensory integration therapy seeks to mitigate these behaviors by teaching how to incorporate information gathered through the senses: smell, taste, touch, hearing, and vision, and combine these stimuli with what is already know to produce proper responses.

As with levels of severity of autism, there are also different levels in which autistic children experience sensory integration dysfunction (SID). These levels range from mild to severe and can either manifest in a lack of sensitivity to the environment or a constant state of over-sensitivity.

Sensory integration therapy seeks to teach the nervous system how to process stimuli in a normalized fashion. A. Jean Ayers, Ph.D., was the first to research the process known as sensory integration therapy. She built the foundation of the therapy that has been instrumental in helping autistic children all over the world. Using a variety of sensory and motor exercises for the central nervous system it is actually possible to teach the brain how to accomplish this.

Typically, an occupational therapist or physical therapist is the professional that practices sensory integration therapy. Using various techniques it is possible to improve concentration, listening skills, physical balance, motor functioning, and impulse control in autistic children.

While it is not successful in 100% of cases, sensory integration therapy has been shown to be a valuable tool for helping those with autism cope with their environment and lead a better, more adjusted life. Each autistic child has different symptoms and it is necessary to devise a plan for each individual when initiating sensory integration therapy.

If you wish to find a sensory integration specialist for your child, there are a number of ways you can go about it.

First, you can ask the guidance department at your local public or private school. If you know someone else who has an autistic child in sensory integration therapy, it is always recommended to get a word of mouth referral.

In addition, there is contact information for leading organizations that deal with sensory integration therapy and autism.

Sensory Integration International, located at 1602 Cabrillo Avenue, Torrance, CA 90501, is an excellent place to begin. Their phone number is (310) 533-8338. If you are looking for an actual practitioner, try the American Occupational Therapy Association, located at 4720 Montgomery Lane, P.O. Box 31220, Bethesda, MD, 20824. You can contact them by phone at this number: (301) 652-2682.

It is important to keep a positive frame of mind when dealing with autism. There is constant research and valuable studies that are shedding light onto this disorder and finding new and innovative ways to treat it.

Sensory integration therapy should not be used as a standalone treatment. Diet, nutrition, and fun methods of learning can all help autistic children interact with the social world in a more productive fashion.




Sign up for Rachel Evans' free Autism Newsletter - dedicated to uncovering autism facts and discover more about the various autism treatments available, all of which are covered in Rachel's comprehensive E-book available at http://www.essential-guide-to-autism.com





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Autism Sensory Integration - How Do Sensory Diets Fit In?


One of the best solutions to some of the problems children with Autism experience is sensory integration techniques. Some children with Autism are so uncomfortable that occasional techniques are of little use.

Many people think that the children are really in pain. I do not know about you but if I am in pain it is almost impossible for me to learn anything.

One of the solutions is what is called a sensory diet. Basically a sensory diet is a plan to do a set variety of techniques. They are also done on a schedule.

A good sensory diet needs to be developed with the help of an occupational therapist or physical therapist. The therapist needs to be one with experience working with sensory diets and children with Autism.

There is no one set of techniques that will make up all people's diet. Just the same way typical children respond to many different techniques, the child with Autism will.

Some people will need pressure point therapy. Some will need massage. Others might need scented markers. Children with Autism might get brushed or any combination of these techniques and others.

The occupational therapist or physical therapist will set up the variety of techniques and the timing. They will also train the family on the different techniques so they can be done the same way across settings and people. Having someone with specific training is important to finding a system that will help.

A parent's challenge will be to get all the people involved in their child's life to do the sensory diet. In addition we will still want to use various techniques when dealing with a meltdown or behavior issues.




Would you like more free information? Please register here: http://autismonabudget.blogspot.com/2009/12/free-information.html

Mylinda Elliott is the parent of five children. The third of the five has Autism which was diagnosed early on. The fourth of the five children has Aspergers. She is a self taught expert on Autism Spectrum Disorders. Mylinda Elliott has also worked professionally in the disability world for the past fifteen years. She is considered the "Go To" woman for advice or resources on disabilities.





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2011年11月28日 星期一

Advice For Parents of Children With Sensory Integration Disorder


Some children can overreact when exposed to too much environmental stimuli. This disorder involving the senses is called sensory integration disorder. If your child has difficulty in high stimulation situations and has a high level of anxiety or stress he may be suffering from this disorder. Sensory integration disorder can effect your child's learning development and behavior. It also causes difficulties with processing information from the five classic senses, the sense of movement , and/or the positional sense (proprioception).

This condition is usually diagnosed by an occupational therapist. There is no known cure but many treatments are available. One common sensitivity is to the sense of touch. If your child shows signs of sensitivity to his sense of touch here are some things you can do to make life a little easier for both of you.

1. Choose the fabric for your child's clothing carefully.

Children with SID will find fabrics like wool too scratchy and irritating. Purchase 100% cotton fabrics instead.

2. Be careful when choosing the style of your child's clothing.

Remove any irritating tags on the collar and look for loose fitting clothes.

3. Choose grooming products wisely.

Don't purchase soaps or shampoos with extra additives or dyes. These may be irritating and harsh to your child.

Disorders that may be related to SID

Autism spectrum disorders

Attention-Deficit/Hyperactivity Disorder (ADHD)

Temper Tantrums

Don't worry this disorder is more common than you might think. It's okay. With the right treatment and attention your child will be able to manage herself with this disorder and life can be more peaceful at home.




Ms. Talbert is a mother of three and editor of Healthy Moms - Parenting, Pregnancy, Health and Women's Issues.

She lives in Sacramento, CA with her family.





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ADHD Natural Treatment - Sensory Integration


Did you know that hyperactivity, inattention, and impulsivity are not the only problems experienced by children with ADHD? These three symptoms are just the tip of the iceberg of a whole series of brain and bodily dysfunctions. Many children with ADHD also experience problems with sensory integration - the manner by which our brain sorts out the information received from the five senses. We understand the five senses as separate entities that give different kinds of information, but they actually work together to give us a comprehensive picture of the world we move in, the events happening around us, and our position in relation to our environment.

Children with ADHD often have problems with sensory integration, meaning that their brains confuse one kind of sensation for another, preventing the children from understand what is happening in their environment. When this happens, they seek out more of the sensation to try to understand it, or avoid the confusing sensation out of fear. If you look at the symptoms of sensory integration dysfunction, you'll notice that they are similar to those of ADHD:

Over-sensitivity to sensory stimuli like sight, sound, touch, or movement. When these children encounter unfamiliar sensations, they are either easily distracted (to explore the sensation further) or behave aggressively (out of fear or confusion).
Tendency to under-react to stimuli. Instead of avoiding unfamiliar stimuli, they seek out intense sensory experiences like spinning in circles or crashing into people. Children with this symptom are usually thought to be hyperactive.
Unusually low or high activity levels. They are either constantly on the go or easily tired.
Problems with motor coordination. They may have poor motor coordination and encounter difficulty learning tasks that require balance or other coordination skills.
Difficulty with daily tasks. Despite having average or above average intelligence, they may experience problems accomplishing mundane activities like tying shoelaces.

If your child experiences any of these problems along with the core symptoms of ADHD, he or she may benefit from sensory integration therapy. This natural, non-invasive treatment aims to correct abnormalities with sensory information processing so the child can perform daily tasks or encounter new stimuli without difficulty. During sensory integration therapy, a child will be placed in what looks like a normal playroom. With the help of a licensed therapist, the child will perform certain activities that combine sensory input and motion, like swinging in a hammock, balancing on a beam, or doing crafts that involve glue, sand, and other textures. The sensory integration sessions are based on these four principles:

a) Just Right Challenge - The child should be able to accomplish the tasks presented as play.

b) Adaptive Response - Using certain strategies, the child should learn to change his or her behavior in response to challenges.

c) Active Engagement - The child should show active participation and enthusiasm when performing the tasks.

d) Child Direction - The tasks and activities during the sessions should follow the child's preferences.

Consult a qualified occupational therapist for a thorough evaluation and ask their advice to see if sensory integration therapy is the right treatment for your child.




Dr. Yannick Pauli is an expert on natural approaches to ADHD and the author of the popular self-help home-program The Unritalin Solution. He is Director of the Centre Neurofit in Lausanne, Switzerland and has a passion taking care of children with ADHD. Click on the link for more great information about adhd natural treatments.





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2011年11月27日 星期日

Bean Bag Chairs for Autism Sensory Integration Therapy


Beanbag chairs have been a casual alternative for comfortable, stylish seating since the 1960s. They come in different sizes and colors, and sometimes different shapes, too, so that they mold themselves to whatever shape you sit in for maximum comfort. For many years, furniture manufacturers made bean bag chairs with small polystyrene beads, but because they posed a choking hazard for young children, manufacturers now make bean bag chairs with shredded polyurethane, the same material that lines car cushions. As a result, bean bag chairs are more comfortable than ever, and with a growing array of fabrics and materials for colors, they've experienced something of a resurgence as a viable choice for informal interior decor. However, bag chairs aren't just stylish and comfortable. Many therapists use them in different ways to help people on the autism spectrum cope with sensory processing issues.

Many individuals affected by autism have neurological issues that affect their ability to process and organize sensory information. They may experience delays in acknowledging what they see, hear or feel, or they may feel sensory input more or less intensely than neurotypical people. This can be very unsettling, and may trigger upset, restlessness and even anxiety in an autistic person. Bean bags are a safe, gentle way to help a person with autism organize their sensory input and have a greater awareness of their bodies in their immediate surroundings. Many physical therapists use beanbag chairs as part of a comprehensive treatment plan for sensory integration issues in autistic kids.

As seating, beanbag chairs provide immediate sensory feedback to the child about every subtle shift in his movements. The child can feel the countless small pieces of shredded polyurethane adjusting beneath the chair's cover. This can also help a child learn more about his body's responses and how to better monitor what feels comfortable to him and what doesn't. Learning to pay attention to his body's sensory cues is an important part of helping a child cope with sensory processing issues. Children can easily take bean bag chairs with them in a therapy session, if a session of therapeutic services require the child to move from room to room.

Many kids on the autism spectrum who also struggle with sensory processing difficulties benefit from deep sensory pressure massage and feeling weighted objects around their torsos. Bean bag chairs are an inexpensive option for providing this purpose. Placing a child on a beanbag, and then placing a second bean bag over the child's torso is a safe method to provide some weighted pressure evenly distributed across the torso. Many autistic kids find this extremely relaxing and comforting.

Bean bag chairs are a safe, gentle option for physical therapy that must involve gentle weight-lifting to improve coordination and muscle tone, both common problems for young children on the spectrum. Children can lift the chairs easily with little coordination necessary, and a dropped bean bag chair, unlike a traditional weight set, won't cause any injury or damage.




With the many features and benefits of bean chairs, buying one which provides the comfort and affordability necessary to meet your needs is crucial. Comfy Sacks has bean bags in a wide variety of sizes and colors. Instead of being filled with beans, they are filled with a proprietary blend of shredded polyurethane foam. This guarantees that it will be soft, and durable for years to come.





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Parenting a Child with Sensory Integration Disorder


After suffering another incredibly stressful morning trying to get my 5 ½ year old son dressed, I've come to the conclusion that there must be other families who go through the same frustration every morning. Most just wouldn't believe that we have it different than anyone else who has young kids. When I'm talking to someone about Jeremy, my stress shows but the explanation is too long so I don't usually elaborate. Their usual answer is "sounds like a typical 5 year old". I guess I've grown used to that. What is harder is to hear from other people who are trying to be helpful that we have a "discipline problem." They offer their typical advice of how to reign a child in and get them to behave.

The fact of the matter is, is that he is NOT a typical 5 year old! Oh, Jeremy loves to play instead of work, throw rocks and finds an empty box utterly fascinating, but the day to day events of our lives, the usually mundane things, are stressful and incredibly different.

This morning was supposed to be a lot of fun. We all woke up early to take a trip to Miami to see my husband's family. It's a 3 day weekend so we wanted to get an early start on Saturday morning so we could enjoy the afternoon in Miami. My husband got up and made coffee, I wrapped about 6 gifts that we're bringing and Jeremy started pulling out clothes and toys he wanted to bring.

I encouraged him to bring the clothes and toys into his room but instead more and more toys got dragged into our living room. When it was time to sit down and eat his breakfast, his favorite of 'waffles and cream', the battle started. Normally, a good tactic is to put a clock in front of him so he can see how much time he has. Today we didn't do that because we were not thinking about the exact moment we had to leave like we do every day for school. That was a BAD CHOICE on my part. I should have showed him the exact time he needed to have eaten and gotten dressed by. Then we should have marched out the door. Unfortunately, we had to pack our suitcases and pack the car.

When Jeremy got to the table ate a few strawberries and milk and got up. My insistence of him sitting and eating finally got ugly after about 15 minutes. While I was running around trying to get everyone ready to go out of town; I continued to put him back in his seat and demand that he eat. I sat with him for about 5 minutes and he didn't eat. I told him he could get a star for his chart if he ate, and got dressed. He started whining and crying so I took a star away from his chart that we've created. On one trip to the bedroom he started playing with a tractor. When I found him again ( I was now taking a shower) he wanted to bring the tractor to the table. I told him NO and to get back to eat. He was screaming and crying because now he wanted the tractor and then he said that "you are the only mommy in the world who is mean to me every day". That is when I told him that if he said that one more time he would get his mouth washed out with soap. (This works wonders for those awful things that kids tend to say sometimes but If I could live without ever doing anything drastic like this, I would!!!)

That stopped the complaining about how "mean" I am but the whining continued. I had to finish feeding him myself in between his tears. He finally finished eating after about 45 minutes. I had turned off the TV by this time of course. I've learned that having the TV on or light music can easily overwhelm Jeremy.

Next, getting him dressed was no easy feat. The first shirt I put on didn't feel comfortable. This was a brand new pre washed long sleeve t-shirt from Osh Kosh. It's darling, but unfortunately, new clothes rarely stay on my son. He prefers old and soft. Many of his very favorite clothes and shoes have spots and tears, but they are the only ones that I can get him to stay in. This morning was no different. I put on Gap underwear, Osh Kosh Jeans and the Osh Kosh t-shirt. After he was completely dressed, he started screaming and wailing about the shirt being too small and the pants being too big. So, off the clothes came! And it wasn't just a calm, "mommy I'm taking off these clothes", it was a screaming crying whining fit accompanied by throwing his clothes across the room which landed on my husband's face as he was walking across the room. At least today he didn't RUN when it was time to get him dressed. That is the typical scenario. He races across the room when it's time to take off his pajamas or time to get changed any time. I can't figure out why! I don't know if that is his body having an automatic reaction to change, or if it's a behavior issue. But it's something that we want to work on in occupational therapy.

Because I already know the drill, that nothing I can say or do will make him keep clothes on when he doesn't want to wear something, I went to the drawer and brought out the old favorites. The yellow long sleeve t-shirt with the #63 and the army looking pants that are soft and comfy. If you see Jeremy out of his school uniform, this is more than likely the outfit he'll be in.

I think of all of the hundreds of dollars that I've wasted by buying clothes that don't quite feel right. I think of the dozens of pairs of shoes that he has kicked and screamed about. I have thrown out piles of socks that just didn't have the seam in the right place. Getting Jeremy dressed to go anywhere, is a struggle nearly every single day.

Recently, the school had a second hand sale on uniforms. I felt like I struck gold by finding the oldest shirts in the school. To me, that means, the SOFTEST and that is perfect for my kid! He is 5 years old, and he wants to wear size 12 shirts. They are big and don't cling to him. Also, discovering the GAP undershirts has been a miracle in our lives. My friend Diane has a red head boy (I believe red heads are more sensitive) and they recommended the GAP undershirts.

I remember trying to get Jeremy dressed at age 2 was no different than now. He went to the Montessori school and because it was pre-school, they weren't particular on the time we arrived. Many, many mornings Jeremy would fight and scream when I had to get him dressed. He would have been perfectly happy staying at home watching TV all day. He would be completely happy just doing that every day of his life. But, fortunately for him, he has two incredibly active parents who rarely ever sit around and watch TV. We have our traditional "Friday night movie night" but we don't watch TV much during the week.

Jeremy does get to go to After Care at school if he's had good behavior the day before. There, they run around the fields, play ball, climb on the jungle gym, have snacks and play with their friends. He loves it! I find that it's the best place for him since he races the kids and exerts more energy there than anywhere else. The hardest part is when it's time to go. What else? He runs away! My mom has found it completely embarrassing because he doesn't pay attention when it's time to come. He just continues playing and then runs to the other side of the field where he can't even hear us yell for him.

By reading books like "The Out of Sync Child" and talking with other mom's I've found a few things that work in this situation. First of all, when you get there, allow the child 5 minutes or 10 minutes to play. Tell him/her that he has 5 minutes and then it's time to go. For Jeremy, he then gets time to transition to the next activity. And the expectation is set. Our new rule is that he is able to achieve a star for his chart at this point. If he comes immediately after the 5 minutes is up, he can get a star for that which when added up every day can determine whether or not he gets to go to after care the next day. He needs to get 5 stars a day - for getting out of bed quickly, for eating and taking his plate to the sink, for making his bed, for getting dressed (almost) by himself, brushing his teeth and hair, etc. He has the chance to earn 3 stars in the morning. Several of the above list is combined into one section for instance: putting dishes in sink and making bed = one star.

The chart system is working for us pretty well. He gets stars taken away for negative attitudes or whining. One day he ripped all of the bad and the good extra stars down. He didn't realize he also ripped the good ones down. Jeremy can earn EXTRA stars for having excellent behavior like the day he had such a great attitude one morning. I was so pleased and so proud of him that he got to go to After Care that day even though he didn't have enough stars the day before. The extra stars can accumulate to 20 and then he gets to go to Toys R Us to buy a toy. So far, he has only a couple of extra stars for good behavior.. and believe me.. I'm looking!

It's hard for Jeremy's self esteem to have these problems. He's gotten in trouble nearly every single day at school. He's come home many times saying, "I'm a bad kid, I'm a bad kid", which really rips out my heart! The system of putting their "apple or acorn" in the yellow, or red basket brings a reputation of "bad behavior". Jeremy has also had his apple on the teachers' desk many times. If he gets bad behavior like this, they take him out of recess. They'll take him out for 5-10 minutes or even the whole time! When I learned this, I freaked out! Jeremy NEEDS activity in order for his brain to FUNCTION correctly. By taking him out of free time outside, they're just hurting the situation. I caused a stink about that at the school and I think they've made some adjustments. The school counselor is now involved and helping to guide the teachers in working with Jeremy. It's truly been a collaborative effort.

Jeremy has also been slow to finish his work. We had him professionally evaluated and it was also discovered that he has auditory processing disorder. This doesn't allow him to process more than one thing at a time. He can hear well, but he can't focus on more than one thing at a time. It doesn't allow him to hear people calling his name if he is immersed in another activity. Next summer, he'll be doing a 10 day intensive program for auditory processing which includes 2 hours in the morning and 3 hours in the afternoon. He'll be listening to headphones which somehow reprogram his brain to hear more than one thing at a time. I am really looking forward to this time to see if we can correct some of the behavior that he has.

We've found a few things that can work for Jeremy in regards to his behavior at school. First of all, Jeremy is OFF of all sugar. He used to have waffles with syrup every morning and all of the sugar gave him too much energy and he was bouncing off the walls! We finally realized that sugar has adverse effects so he now gets little if any sugar in the morning. We even prefer milk over orange juice since fruit has sugar in it.

Next, Jeremy has to take time to exercise in the morning. We put a mini trampoline in our living room and he bounces a few hundred times in the morning before school. If we have time, my husband will take him out to ride his bike before school or run around the field and play Frisbee. On mornings that he doesn't get to exercise, he seems to be more talkative and figity at school.

I've had to explained to Jeremy that sugar is "poison" to his brain. It makes him react in such a negative way where he throws fits and disobeys. I seem to automatically know when he's had sugar! When he acts like this and I know he's not overtired, I automatically ask if he's had sugar!? Usually, the answer is yes and so then I require him to start bouncing on the trampoline to get the energy out.

Jeremy might also have ADHD, which is a possibility since he was a preemie and upwards of 40% of preemies have ADHD. I went to one doctor and within about 1 minute he was telling me that Jeremy had ADHD and would require medicine! That appalled my husband and I was quite put off myself. Even if Jeremy does have ADHD, we're not going to put him on medication without trying to find every other way to manage it first. Besides occupational therapy, we've heard of other therapies that families have used and have had great success. Besides monitoring diet, they've used biofeedback and also some sort of testing of the electrodes in the body to eliminate toxins. I may have those details wrong, but we haven't gone down that road yet. Right now, Jeremy is in Tae Kwan Do 2 times a week. There, they teach self discipline, self esteem, leadership and focus. These are all qualities that I want for Jeremy.

If anyone could have told us where we'd end up even 6 months after we started down this path, I wouldn't have been able to handle it all at once. When we first discovered it, people came out of the woodwork to tell us their discoveries and what they went through. A friend from high school confided in me about her family situation and how they dealt with it. It was hard on her husband to imagine that their kid, coming from two "over achiever " parents, would have developmental problems. I could relate to that of course, but when she started telling me that her child couldn't stand loud noises and would cover his ears and cry and scream, I couldn't relate to THAT. She also told me that it'd be best for Jeremy to repeat kindergarten and at the time, it was a thought that I couldn't bear. We've since determined that Jeremy will repeat kindergarten next year. Coming to that conclusion took a lot of time and was a result of visiting numerous pre schools, talking with our own principal, vice principal, other parents, his teacher and the counselor. It was our principal who encouraged us not to do anything rash. I trusted her and I kept him in school and made the decision early on to repeat next year.

Other parents of kids of SID children had other stories. One parent's child had low motor skills and didn't want to swing or play with other kids. That was completely OPPOSITE of Jeremy. I did meet one mom at a workshop for parents with kids of SID who is very similar to Jeremy. He's a "crasher" and needs just as much physical stimulation as Jeremy. We laugh over the fact that we TELL our kids to jump on the couch... instead of getting off of them. So, little by little, with more reading and more talking, I found we all had one thing in common: MAJOR FRUSTRATION!

My friend from high school also had some of the same issues I was facing at home. My husband, who is a complete overachiever, couldn't deal with the fact that it was recommended that Jeremy go on medication. He absolutely REFUSED to even consider the possibility and so this would create lots of tension. My resolve was to find a solution, whatever that was. I was dealing with the teachers and with Jeremy every day, not just in the morning or at bed time. When I took Jeremy to school, the stress stopped for my husband, but not for me or his teachers. After speaking with numerous wives, I've discovered that the husbands don't believe it, or WANT to believe it. It appears that because men feel that they must be strong in every situation and must handle many obstacles in life, and that having a son that is facing problems is just too much to bear. Most of the dads of the boys with SID are in denial at first. The wives tend to have to deal with finding out what the issues are all by themselves by researching, talking and finding solutions. Many of the husbands fight the wives to the end until the wife finally convinces her mate to "just speak with an expert". In one case I know, the father uses the excuse, "he's just like I was" so he assumes it is okay. Meanwhile, everyone including his wife is going crazy having to deal with his child. My friend is of the mindset that if there IS help available, then she's going to get it! In reality, many of these men are right, because the kid IS just like them... and if there would have been help for their own mothers way back when, then the moms more than likely would have taken it instead of suffering through it and of course it would have made everything easier on the child. They could have learned tactics that would have helped them manage their actions, their bodies and their behavior.

My husband finally came around when he was able to speak with the Occupational Therapist where we got Jeremy evaluated. They promised to do whatever possible to work with Jeremy to correct many of these issues. The whole topic of using medication to help Jeremy hasn't come around for a while, but I know that my husband will be open to it if we have to do it. He's had to deal with Jeremy while I've been out of town and it nearly put him over the edge.

We're really just starting on this journey to getting the help we need. I've discovered many successes through trial and error. I've found that having a chart that rewards Jeremy for his chores and responsibilities for the day motivates him better than punishment. Tae Kwan Do has been fantastic to improve his self esteem. Talking with the teacher on an almost daily basis alerting her with new research I've found or discoveries that have happened has really helped. Daily massages on his feet, legs, back and hands are helping the stimulation of his skin so he doesn't freak out quite as bad when putting on socks and shoes. Teaching him to breathe himself through frustrations is an ongoing process and educating him about what to feed his body to it works correctly has helped me just as much!

Had I known what it would take to parent a child with Sensory Integration Disorder, then I would have said that I didn't have what it took. And I probably would have been right. My stress level has been through the roof ever since I had Jeremy but in reality finding out that he had something that was actually diagnosed gave me the power back! I knew that if I educated myself, our situation would improve and indeed it has.

I'm now able to understand that I need to implement complete structure in order for him to function at his best. That structure does include plenty of free or down time, but when it's time to do something or go some where, I put on my "drill sergeant" hat to get him to perform. It goes against my nature to be that firm, but I've learned that in order for our family to function, then I have to do what I have to do.

Please feel free to share your stories with me or to reach out for support. Perhaps if several of us can reach out to others to help, then others will be able to educate their spouses, their teachers and their friends.




Mary Gardner is an executive communications consultant and lifestyle coach. She is the mommy of Jeremy, a precious and active 5 year old boy who has Sensory Integration issues. Mary can be reached at mary@marygardner.com





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2011年11月26日 星期六

SID - Sensory Integration Disorder and Neurofeedback


Sensory Integration Disorder (SID) was discovered by Jean Ayres, Ph.D. about 40 years ago. Symptoms of SID in children are often misinterpreted as psychological problems or just plain bad behavior.

Higher cognitive functions including things such as learning and behavior depend upon having normal sensory integration.

As a psychologist, I am sad to say that when I was in graduate school, (1982 - 1987) that this disorder wasn't talked about much. At this time I am often involved with families who have a child with Sensory Integration Disorder.

Imagine, if you will, that for each of your 5 senses, there is a wire of a different color that leads the information form that particular sense, into your brain. For example, for the information that comes in from your eyes, or your visual senses, you might imagine a red wire; and blue one for hearing (auditory), etc.

Now, assuming that your brain was able to notice what color of "wire" the information was coming from, and knew that the red "wire" was information from your eyes, and blue was from your ears, it would be a fairly straightforward process for keeping things figured out. Someone with SID, however, doesn't experience it quite like this.

When someone is dealing with SID, their brain is getting mixed signals. At times, the red "wire "might be visual information; at other times, it might be the blue "wire" that is shuttling the visual data. Then, there may be times when the red "wire" is carrying both visual and auditory information. Can you see how this might be very confusing for the brain to interpret?

This sounds like a rather complex challenge, does it not? One could argue that it is, I suppose, but I've never been one for building a "case" for difficulty. Instead, I prefer to gather evidence for possibility.

In short, when neurofeedback is helpful for those with SID, it's as though neurofeedback is able to teach the brain to start recognizing the "wires" accurately and stop acting "color blind" when it comes to incoming sensory information. And, why shouldn't everyone's brain learn to clearly interpret sensory information?




Want to know more about the amazing world of Neurofeedback? Click on this link to go to http://www.NeurofeedbackBook.com Dr. Clare Albright is a psychologist and the author of a 168 page book, "Neurofeedback: Transforming Your Life with Brain Biofeedback" and can be reached at (949) 454-0996 http://www.NeurofeedbackBook.com. The pdf version of the book can be downloaded for only $7.99!





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Alternative For ADHD - Discover the Truth About Sensory Integration Therapy and ADHD


Probably the most famous treatment for persons with ADHD is pharmacotherapy. Why is that, you may ask. Well, that is because when children, let us say your child is diagnosed with a condition, the first professional that you may think can help you are doctors. Yes, that is correct; they can help you. However, you should know that the help they can provide you is limited. They may know a lot about ADHD but the treatment approach that they are trained to perform is limited into prescription of medicines. However, they know the right persons who can attend more to your child's problem that is why there are things like referrals.

Now, let us first have an overview of ADHD. It is a neurobiologic disorder that has three hallmark features; that is inattention, impulsivity and hyperactivity. Now, here comes the tricky part. Most of you may think that these symptoms are purely behavioral, but you are wrong. There is actually what professionals call the sensory integration dysfunction. Now, what exactly is sensory integration? It is the ability to process, organize and synthesize sensory information that a person may receive from the body and/or the environment. Most of the time, it is the children with Autism that usually have sensory integration dysfunctions. However, there have been cases of children with ADHD who also have Sensory integration (SI) problems. These SI problems may manifest either the child will withdraw or seek a particular sensation. In your child with ADHD, his or her hyperactivity may actually be a sign that your child is seeking a particular sensation. Therefore, treatment approaches like behavior therapy would not work in your child, thus the Sensory Integration Therapy. This is an alternative for ADHD treatment which makes use of sensations and will manage your child's behavior through giving your child the amount of sensation that your child is seeking. After this has been achieved, there will be an immediate and significant change in the behavior of the child. Your child may be more attentive in the tasks assigned to him or her. Although there are studies proving its effectiveness, for some, these studies are still insufficient. Therefore, there still are debates regarding this intervention approach. However, these are still used in clinics but those who perform it do it carefully.

This information only means that there are still a lot to learn about ADHD and that the problems that your child may have may not be what you expect. So if your child is not responding to a treatment approach, this may mean that this is not your child needs, and so you may study more about the condition and ask question to expand your knowledge.




Puneet writes a blog about ADHD and helps ADHD sufferers to find new treatments in naturopathy and alternative medicine. If you are looking for a well-researched herbal remedy for ADHD, you may read more





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2011年11月25日 星期五

Understanding the Links Between ADD/ADHD and Sensory Integration Disorder


Many frustrated parents are unaware of the similarities and the links between ADD/ADHD and Sensory Integration Disorder. In fact, many people have not yet heard of it. Sensory Integration Disorder is basically a condition whereby the brain is unable to fully utilize the information gathered through the senses in an effective, organized way.

Children with sensory integration disorder (SI) may have difficulty finding the right balance to react to information received. Sufferers tend to react in extremes to things such as touch, smells, sounds and tastes that other people take in their stride as part of their daily life.

A child with this condition will display extreme and anti-social behavior as the senses are experienced. The behavior could involve extreme emotional outbursts, crying, tantrums and more. Parents' first instinct is to assume that the child is trying to get attention through this behavior when in fact it is sensory integration disorder.

Kids with ADD/ADHD and SI disorder will display a number of other symptoms. Kids with hearing sensitivities will hear noises that other people do not hear, such as people chewing or breathing or other background noises.

Children with touch sensitivities will be indifferent to temperatures or pain. They will refuse to wear clothes made of certain fabrics or wear long sleeves even in summer to avoid skin showing. They may also avoid physical contact with other people. They are also likely to avoid grooming and any activities that involve touching their faces, hair or teeth. Kids with ADD/ADHD and SI may have very low or very high activity levels, spin things around and taking things apart.

The brain is unable to process and interpret information that is entering properly, which causes them to be unable to form a proper impression from the combined information of all the senses. Parents are likely to view the child's reaction as misbehavior, but the child suffering from ADD/ADHD and sensory integration disorder is probably very fearful and confused.




Lizette has extensive experience in creating home education tools and resources that are available freely from http://www.twinstaracademy.com/

She also has a lot of experience in dealing with an ADHD child, thanks to her 9-year old daughter. However, she has found benefit from Minerals for ADHD





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Autism Sensory Integration - Where Do Parents Start?


Unfortunately in this day and age there are still people who do not see Sensory Integration as a treatment therapy for children with Autism. Unfortunately many people do not see it as a therapy in its own right.

It is a therapy so intense that is can be puzzling and daunting to people. It is also a therapy so simple with gains that are so important and significant. Whether working with a child who is over sensitive or under sensitive there is help to be had.

The first thing for a parent to think about when considering Sensory Integration is being able to suspend their thoughts and feelings. They have to be able to do that to acquire the empathy of thought and feeling needed to figure out what to do to help their child.

If a child is screaming because they are over sensitive to their environment they will not be able to learn. If a child is so under stimulated that they can not work up the energy to engage they will not be able to learn.

Parents can help a child with Autism that has these characteristics. There are several areas associated with Sensory Integration. These areas are oral, tactile, aural, visual, and proprioceptive. Another way to say this is mouthing, touching, hearing, seeing, and being able to tell where your body is in relation to people and things.

Early consistent speech therapy is critical to a child with Autism. Some children with and without Autism may not need speech therapy or as much speech therapy if they get it early. The same theory works with Sensory Integration.

Early consistent Sensory Integration in all areas may help a child to the extent is may not be needed or needed to that level later. It is not voodoo or magic. It is a consistent application of techniques that work.




Would you like more free information? Please register here: http://autismonabudget.blogspot.com/2009/12/free-information.html

Mylinda Elliott is the parent of five children. The third of the five has Autism which was diagnosed early on. The fourth of the five children has Aspergers. She is a self taught expert on Autism Spectrum Disorders. Mylinda Elliott has also worked professionally in the disability world for the past fifteen years. She is considered the "Go To" woman for advice or resources on disabilities.





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Sensory Integration Dysfunction - What Is It, Diagnosis, And Treatment


Is your child with autism over responsive to sensation which shows by withdrawing from touch, or getting upset by loud noises? Or is your child under responsive to sensations which shows by hyperactivity, unawareness of touch or pain, and likes loud sounds? Your child may have sensory integration dysfunction, which could be affecting their education and life. This article will discuss what sensory integration disorder is, and also about diagnosis.

Sensory integration refers to our ability to take in information through our senses (touch, movement, smell, taste, vision, and hearing), interpret that information, and respond to it. Sensory Integration Dysfunction (SID) is the inability of the brain, to correctly process information brought in by the senses. People with SID may misinterpret everyday sensory information such as touch, sound and movement.

Below are a few symptoms of SID:

1. Loves to spin, swing, jump-this may calm them down,

2.Complains that some clothing feels scratchy, or doesn't like tags,

3. Picky eaters-doesn't like how some foods feel in their mouth,

4.Over sensitive to smells or sounds-may sniff people or food-will frequently cover ears to sounds,

5. May have high pain tolerance,

6. Can be impulsive or distractible.

The Star Center puts out a checklist for Sensory Integration Dysfunction. The Star Center calls it Sensory Processing Disorder (SPD). Below are a few items on the checklist:

1. Difficulty eating,

2.Resists cuddling or holding,

3.Easily startled,

4.Over sensitive to stimulation,

5.Difficulty learning new motor tasks,

6.Constant movement,

7.Overreacts to touch noise or smell,

8.Appears clumsy and stumbles a lot, and

9.Avoids visually stimulating environments.

SID could be affecting your child in many different ways. There are two separate types of SID: Sensory Avoiding and Sensory Seeking. Children with sensory avoiding do not like to be touched or cuddled, they are fearful of fast movement, are cautious and unwilling to take risks or try new things, are very pick eaters and do not like to be in loud or busy environments. Children with sensory seeking can have hyperactivity, unawareness of touch or pain, take part in unsafe activities, enjoy sounds that are too loud.

Children with Sensory Integration Dysfunction may also have motor skill problems. These children may have: 1.Poor fine motor skills, 2.Poor gross motor skills, 3.Difficulty imitating movements, 4.Trouble with balance, and 5.A preference for seating activities, such as video games.

To determine if your child has SID, they should be evaluation by a SIPT qualified occupational therapist (OT). Many school districts hire occupational therapists, but may not be SIPT qualified, and therefore not qualified to test in this area. You may need to advocate for your child to have them tested by a SIPT qualified OT.

Treatment for SID is occupational therapy, by a qualified therapist. Check with your school district to see if there OT has experience with Sensory Integration Disorder. If they do not, consider getting an Independent Educational Evaluation (IEE) with a SIPT qualified OT. Make sure that the evaluator makes specific recommendations on amount of therapy needed, goals and objectives.

By understanding what Sensory Integration Dysfunction is, how it is diagnosed and treated you may help your child. SID can negatively affect your child's life, but with proper treatment you child can reach their potential.




JoAnn Collins is the mother of two adults with disabilities, and has helped families navigate the special eduation system, as an advocate, for over 15 years. She is a presenter and author of the book "Disability Deception; Lies Disability Educators Tell and How Parents Can Beat Them at Their Own Game." The book has a lot of resources and information to help parents fight for an appropriate education for their child. For a free E newsletter entitled "The Special Education Spotlight" send an E mail to: JoAnn@disabilitydeception.com For more information on the book, testimonials about the book, and a link to more articles go to: http://www.disabilitydeception.com





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2011年11月24日 星期四

Autism Sensory Integration - Large Tools


There are a lot of different tools that parents can use for sensory integration for a child with Autism. Sensory Integration is one of the answers to calming our children during times of stress. It does not matter where the stress comes from the techniques know about sensory integration seem to help. Sometimes parents will not even know the reasons for a melt down.

There are several large tools parents can look at using with their child with Autism. Some of those tools are perfect for parents looking for 'Autism on a Budget' techniques, especially when some of those techniques are free ones. As always you have to try different ones out to see if they work.

One of the easy large tools is the local play ground. Many children with Autism respond to swings. The back and forth motion seems to be calming to them. Even twisting the swing around and around and letting it go back is soothing to some children with disabilities.

Some parents will find putting a swing in their yard will help so that they have quick access. Do you remember the old tire swings that used to be in backyards? This could be perfect for a child with Autism to hold on to and use, as well as easy on your budget.

Yes of course you could buy more expensive swing sets or even the more expensive 'specialty' swings that are sold for occupational therapy. I am sure there will and are other things that you will need to buy or pay for that may or may not be as easily handled.

Another large tool parents may want to add to their tool chest, if you will, is a ball pool. Many fast food playgrounds have ball pools or ball pits. They have the hollow balls in some type of container, which the child can get their whole body into.

The balls are three to five inches in diameter and very light weight. Something about the feel of all the balls touching them is soothing. As well as children just like to throw them around.

Many parents of children with Autism have purchased a children's plastic pool and filled it with the hollow balls. They keep this in the house for their child. Children do need supervision when playing with the ball pool. Even though it is a bit of a mess having balls all over their room or the play area, DO NOT use any type of covering. Young children in particular have been hurt when a covering has been used to control the mess.




Would you like more free information? Please register here: http://autismonabudget.blogspot.com/2009/12/free-information.html

Mylinda Elliott is the parent of five children. The third of the five has Autism which was diagnosed early on. The fourth of the five children has Aspergers. She is a self taught expert on Autism Spectrum Disorders. Mylinda Elliott has also worked professionally in the disability world for the past fifteen years. She is considered the "Go To" woman for advice or resources on disabilities.





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A Personal Overview of Sensory Integration Dysfunction


My young son, Joseph, was born in September 2006. I was delighted to know he'd be joining our family, but we needed to have an emergency C-section. I had been pushing for two hours and he was starting to show signs of distress. He was born at 2:11 am, nice and pink with a "Harry Potter" scar on his forehead that went away after a few days. Unfortunately, what might have occurred during his birth was some neurological damage which left him with Sensory Integration Dysfunction.

I didn't notice something was wrong until Joe was about eighteen months. He met all his physical milestones - in fact, he made them earlier than my first son. At eighteen months though, Joe wasn't talking. He didn't seem to know "Mommy" or "Daddy." He threw toys for no reason, as if he needed to throw them. He also covered his ears with his hands often, which we didn't understand. He hardly got sick or had ear infections. We knew he wasn't autistic, but we also knew something wasn't quite right. Our pediatrician recommended us to our Regional Center, in charge of Early Childhood Intervention. (Every state should have an Early Childhood Intervention Program.) Joseph was evaluated with severe cognitive and speech delays. He was twenty-months-old at the time of the evaluation, but presented with the cognitive skills of an eight-month-old. My husband and I were stunned. Joe began receiving child development, speech, and occupational therapies. At twenty-seven months, he began group therapy.

After six months, Joe had closed some rather daunting developmental gaps. A re-evaluation at twenty-nine months showed him at twenty-two months cognitively. Still, we had no idea what was the cause. Joe's occupational therapist review had the clues we needed to determine what he had - Sensory Integration Dysfunction.

Known as SID or DSI, (so as not to confuse it with Sudden Infant Death Syndrome SIDS) Sensory Integration Dysfunction is where the brain perceives sensory input normally, but misinterprets the information. This misinterpretation leaves the child in a hypo or hyper-active state. Hypoactive is an under stimulation to sensory input and hyperactive is an over stimulation to sensory input. In Joe's case, he's more hypo than hyper-active.

There are multiple causes for DSI, and in fact, it often presents with autism, but it can also present by itself. In my son's case, it was presenting with cognitive and speech delays.

Joe's occupational therapist report documented several sensory seeking behaviors. (As opposed to sensory avoiding/hyper-active behaviors.) He loved to jump, spin, and swing over the norm that children with no sensory issues do. He had a high tolerance for pain and had a high activity level. Joe is also easily distracted by other things. I did a Google search on sensory seeking behaviors and it led me right to Sensory Integration Dysfunction.

To my surprise, I discovered there are seven senses - yes, seven! Hearing, sight, smell, taste, touch, we all know, but there is also the vestibular sense and proprioception sense. The vestibular sense refers to the sense of balance and gravity. Without that sense, we'd be clumsy or awkward in our movements. Proprioception refers to the impacting/compacting of joints. Signs that your child might be sensory seeking in these areas are running, jumping, spinning more than normal (vestibular) and throwing toys just for the sensation of the impacting/compacting of the joints. (proprioception) This was Joe to a "tee."

Other signs of DSI include covering one's hands over their ears, (something Joe used to do a lot, but now rarely does. It was his one sign of sensory avoiding, hyper-active behavior) unusually high or low activity, and very picky eating. (In Joe's case, he needs crunchy, chewy foods to help provide the stimulation he needs to get the proprioception sensation of the jaw's joints impacting and compacting.) More signs involve tip-toe walking (because their feet are highly sensitive to touch), hand flapping (for the proprioception effect) speech delays, cognitive delays, poor balance, unusually high or low tolerance for pain, acting impulsively, and an unusually high or low activity level. There are many other symptoms which you can research online. There's also a wealth of information on the Internet regarding DSI and there are several well written books on the subject alone.

An occupational therapist is essential in helping the family with a DSI child. They can help identify DSI behaviors and establish a "sensory diet" for a family to use when their child shows signs of sensory seeking or avoiding behaviors. In fact, A. Jean Ayers, an occupational therapist, was the one to identify the dysfunction.

DSI is a dysfunction, not a disease. It can't be cured, but managed. Though early childhood services, my son is thriving and we're managing his DSI now. It's still an adventure for us, but recognizing DSI symptoms early will help your child get the services he or she needs.




Steph B likes to read many books and a variety of different genres. Steph B is an author at Writing.com which is a site for Creative Writing.





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2011年11月23日 星期三

Help Kids With Sensory Integration Disorder Tolerate Transitions and Change


To kids with sensory integration and sensory processing issues, the world is filled with abrupt and unpleasant transitions. What seems to us to be an easy shift in activities may be, to them, like slamming on the brakes and or making a sharp turn that causes them to feel disoriented. To transition a child, first, get her attention. Call her name and tell her that she is going to switch activities soon, and give her a time frame for completing the switch. For an older child, you might say "In fifteen minutes you need to do your homework..." and set a kitchen timer. For a younger child, you might say "when you've gone down the slide three more times, we're leaving the park" and encourage her to count each of those last trips down the slide. Keep your voice inviting and warm but firm when you give warnings about transitions.

Remind the child of the positive aspects of the new activity he will be switching too. Even if it is not his favorite task you can remind him of the upside. If he has a dentist appointment, remind him that the dentist has that box of terrific toys to choose from when the appointment is over. If he doesn't like to leave the park, tell him he can choose the music for the car when you drive home.

To help him switch gears when time is up, the sensory child may well need some sort of calming or focusing activity. Climbing some stairs, marching, stretching, having a nonsugary snack, doing jumping jacks, or engaging in a fun little shuffle race (shuffling provides a lot of good, strong input to the legs) may be what he needs to regroup and ready himself for the next activity on the agenda.

If the child resists a transition and protests, think of it as an old car making creaky noises as it starts up in cold weather. Don't give the resistance too much attention, but do give her some time to adjust to the transition. Ask yourself, does this have to happen instantly or can you take a few more minutes? Plan for extra transition time, because the more patient you are, the easier it will be to diffuse her anxiety about the switch. As you observe her carefully, you'll see which transitions are the most difficult for her and be better able to prepare her. Use calendars and clocks, even with young children, to give them a sense of what's coming up.

Remind her what she needs to do to prepare for the activity ("You'll have to dress warmly to go on the walk"). Don't assume she will account for the preparation time, such as gathering the materials to do her homework, or the clean up time, such as putting away her toys. Leave plenty of time for her to accomplish these activities and praise her for doing the prep work or cleanup, offering a sense of how long the activity took: "Good for you! You got all your dolls and their clothes put away in just three minutes!" "I know it took ten minutes to find your shoes, coat, hat and gloves and put them on. That was frustrating for you, wasn't it? Let's talk about how to make it easier to find them all so it's not so much work to go outside to the park." Be light and positive as you discuss how long tasks take and what is involved and you can help your child understand the beginning, middle, and end of a task and predict how long each step will take.

Talk to your child about possible accommodations for her concerns and her sensory issues as she switches from one activity to another: "No, we can't make the walk only 5 minutes long, but you can keep your hands in your pockets instead of wearing mittens. You can rub your head before you put your hat on so the tightness doesn't bother you so much. No, you can't get candy at the corner store we'll be passing."

The more prepared she is for any transition, the less anxiety-provoking the transitions involved will be. And whenever you can, cut yourself some slack as you work to help your child transition. It's challenging to do, but in time, your child will learn to better tolerate the unpredictability in his day.

copyright (c) 2010 Nancy Peske




Nancy Peske is the mother of a child with sensory issues and coauthor of the book Raising a Sensory Smart Child: The Definitive Handbook for Helping Your Child with Sensory Processing Issues and sends out a weekly newsletter of practical tips for parents and professionals who work with children who have sensory processing issues, available at http://www.sensorysmartnews.com You can learn more about practical ways to help children with sensory integration issues at http://www.sensorysmartparent.com





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Sensory Integration Deficiency Disorder - More Than Just a Myth


Sensory Integration Deficiency Syndrome, Sensory Integration Disability Disorder, Sensory Issues...Yeah, there are many names for this disorder, and it seems like they're all long and difficult to pronounce. If you've been diagnosed as having this disorder chances are you were diagnosed by an occupational therapist. Hit it on the head, huh? Well, here's why...

An occupational therapist named Anna Jean Ayres was the first one to popularize the idea of a disorder that interferes with the normal brain function of sensory integration. She was by no means the first one to research it, but she was one of the first to publish her findings.

That was in 1989. Today there is still a lot about Sensory Integration Disorder Syndrome that still isn't known. Sorry to change names again, but there a lot of names to choose from.

Most doctors that have actually heard of this disorder don't really know much about it though. Many who do believe it is nothing more than the side-effects of people with autism, attention deficit disorder, hyperactivity disorder, and several other developmental or neurological disorders. It's hard for someone with sensory issues to be taken seriously.

Occupational therapists may be the ones who will be most likely to believe you have the disorder, but don't fool yourself into thinking that's a cure. Many therapists claim to have a cure VIA exposure therapy, but usually when a patient would get better it was usually due to them outgrowing the syndrome on their own.

There's the good news. Many children who have sensory issues eventually outgrow them on their own. This is not every case, but most people who have this disorder and nothing else will outgrow their symptoms.

The major signs that a child may have sensory issues include: sensitivity to touch, smell, hearing, sight, or texture of their food (touch is the one you especially want to watch out for). Sensitivity to getting their hair cut. This one's not always prevalent, but prolonged cases usually involve the child walking on their toes.

Even if you never outgrow the disorder there are many ways to manage it. Walking becomes easier for toe walkers if they lose a little weight. Explaining the condition can also be helpful in dealing with the day to day rigors of basic human contact. If someone touches you in a way you don't like, simply explain it in a calm, mature fashion.

These tips may sound corny or even too simple to be true, but knowledge is a powerful tool, and if you know what's going on then you have power.

Good luck.








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