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Topic : 01/17 Extreme Disorders

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Created on : Friday, January 13, 2006, 02:18:32 pm
Author : DrPhilBoard1

Does your child rage, scream and kick doors? Is his or her behavior the typical brattiness of a spoiled child, or involuntary behavior beyond the child's control? Dr. Phil sheds light on a pair of widely misunderstood extreme neurological disorders. First, he looks at Asperger's syndrome, a high-functioning form of autism which can cause a person to lack control over his or her emotions, including anger. Rich and Karen's 15-year-old son, Alex, was diagnosed with Asperger's at age 6. His sudden fits of rage and erratic behavior have put a strain on his whole family. Should his parents be afraid of Alex, or is there something they can do to bring his behavior under control? Plus, Craig, 37, can't control his physical tics, nor can he keep from constantly uttering obscenities, literally hundreds of times a day. Craig suffers from Tourette syndrome, an affliction that's gotten so bad, he won't go into grocery stores, movie theatres or any public place for fear he'll be kicked out. What will the disorder mean for his plans to start a family? Talk about the show here.

 

Find out what happened on the show.

 

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January 18, 2006, 3:40 pm PST

Great advice..

Quote From: cathy05

I too have a son with Asperger's.  I don't think we were watching the same show.  Dr. Phil mentioned many times that Alex was an extreme case.  My husband and I watched and saw a lot of our son in Alex.  Asperger's is a disorder with extremes, whether it be anxiety, anger, OCD, negativity, and paranoia, just to name a few.   After reading your message, I am saddened.  AS is a disorder.  That is made clear when you look at all of the social and abstract struggles that my son goes through on a daily basis.  He is a wonderful, caring, brilliant soul that can look and act just like Alex when he is anxious about the situation around him.  You yourself mentioned that you were bullied and ate many lunches in the bathroom.  Was that normal?  Of course not.  Your disorder prevented you from socializing "normally" with the world around you and if you had been given social therapy, maybe you wouldn't be so angry today.   

  

My son is getting help (therapy and medication).  The right medication does not change the child's personality.  It helps him to focus and survive in a world that is not forgiving of differences.  It may not be right, but that's what it is.  We can do nothing about the world but we can help our son assimilate into our society so that he may one day showcase the many talents that we see everyday!!!    

  

Children with AS are a gift from God, and with the right help, they can one day shine. 

  

  

Cathy C.  

      I have a 12 year old son, now in middle school. He was diagnosed with Asperger's/ ADHD at 3, and ODD;OCD at 4 years of age.  He is on med and they help  alot.  Both at school and at home. I am raising him as a single parent.  His father walked out of his life when he was 4 years old. And just months after our divorce was finalized.  He was upset because I couldn't make our son do things the way he always wanted. He always said, he was to babied and spoiled. And that as a child he took advantage of situations.  For whatever reason he's isn't very understanding about anything our son is going through!!   I bless my close family's understanding everyday. Even my ex's parents and the rest of his family understand . But, they too find it difficult.. at times  Because we don't fully understand this form of high functioning autism. We have been dealing with issues that arise from this form of autism for so long ..it's become a everyday way of life...since he was born!( He spent the last month in my womb running inside me...and caused small pull away tear's in the placenta.)  I was lucky I was able to spend a lot of time with him as a toddler.  I was never able to place him in a preschool environment because of his hyperactivity, and sensory unpredictability that caused him aggression and panic attacks.   He started K 1  at 5 1/2  he did 3 months.  And was graduated to 1st grade.  He is in a special day class because the classes are small and the curricular activities are done at a slower pace. So doing better in school.. for him is something he now looks forward too.  But,  it just seems to be getting worse every day at home. I feel the helplessness at time because I just don't know how to handle all situations.  I have decide that his being on the med's is a good thing.  It helps him tremendously with focus and with with social activities.  All working  hard to provide him a prosperous future.  I want for him is to have a "normal" life!  If time comes and his need change ..then we'll re evaluate.  But, if it works don't mess with it. But, I believe his biggest problem ..is structure..and that for a 12 year old s all in timing..  It's a fight at times, for me to help my son,  I just wish he had more rights. We live in a society that is backward in many ways.  I get upset when I hear them talking about cutting services and programs for special needs. But, our government programs take better care prison rights, etc and the like.  It cost taxpayers a lot of money to pay for so called lifer's.  Money that could be spent helping people really in need.    I am alway open to advice..so feel free to share : )        Betsy  
 
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January 18, 2006, 3:46 pm PST

Thank you for sharing!

Quote From: infodragon

I am 28 years old and discovered that I have Aspergers only 18 months ago.  I'd like to encourage all parents out there with a testimonial.  Find something for your Aspie children!  Something that they can focus into, that they will be able to channel that energy, which manifests as rage many times.  It isn't a cure all but it can help tremendously.  

  

Being born in 1977, and Aspergers not on the books until 1994, I was a Junior in high school, there were no standard diagnostic criteria, I was into the real-world long before anything really was publicized.  I am of above average intelligence but have never had my IQ tested.  I did terrible in school because I was bored out of my mind.  I tied for highest ACT scores in my graduating class.  I went to a private school that was more challenging than most public schools, I was still bored.   

  

By the time I was 12 I had an incredibly advanced knowledge of Dinosaurs and Astronomy, being my 2 favorite subjects.  My dad had an 8" diameter telescope and subscribed to some Astronomy magazines.   I began to learn about the mathematics of orbits, how comets interacted with planets, and how the gas giants were formed in our solar system.  I knew how fast light traveled, and had a very good grasp of Einsteins theory of relativity.  I did everything I could to learn more about Astronomy.  Dinosaurs were 2nd.  Then when I was 13 for Christmas my parents purchased a PC for the family.  That was "all she wrote."  I latched on to that PC more than anything I had in my life.   I devoted every last second to learning how to exploit the technology in any way.  I worked so hard I gained the attention of a local company that needed some basic programming done.  So I got my first job the week of my 16th birthday.  I far exceeded their expectations and began to work on their higher level software development.  They were developing one of the first digital cameras and I began to implement advanced image processing.  Work became my school and school was my prison.  I was tortured by the unspoken language of social interaction.  I did not get it and I was called a geek/nerd/dork/moron/idiot/...  Every minute of school was a minute of torture, weather it was because I was teased or because I was in a foreign land and could barely speak the language. 

  

When I got to the University, for computer science, I was quickly disillusioned because the first 4 years, I was going to be learning everything I had learned while working.  I had achieved what was required for a bachelors degree, from the technology perspective.  I helped seniors work on their senior projects... 

  

I do not say this to brag, unknowingly my parents introduced that "thing" that I could pour everything of my self into.  My rage drastically decreased.  I would think about programming or whatever on the computer when things became to overwhelming.  I did play games, but I worked more than I played.  Games can be a good distraction but if they are played too much then they can exasperate the problem.  Luckily I learned this and cut back on the games I was playing.  The intensity of the work I was doing soon attracted the attention of the dot boom.  I got a tremendous contract working for a large firm doing software development for more than what my dad was making, at the time I was 19.  I was thrown to the wolves.  Socially I did not fit in, though there were a few like me, and I was accepted for what I was and allowed to work.  I put my nose to the grind stone like I never believed I could.  My social graces were totally lacking and so I could not climb the corporate ladder.  So I began to work on them.  I began to watch what other people did and learned social interaction like I would have learned how to do math.  

  

  

Over the next 6 years I worked on developing my social skills.  Even today I "recite" the liturgy of social interaction when I come in contact with people.  I met my wife 2 years into this, we got married one year to the day later.  She has been a huge asset in helping me develop my social graces.  Of everything that I am she is totally opposite and we celebrate that together!  She was with me when we discovered why I was so "different" and logical.  Anyway, while I was working I noticed a few things that I could do better than anybody else so I started my own company.  That was 8 years ago and for the past 2 years we have been totally self sufficient working for my business.  The stresses are tremendous, of dealing with the people.  Everything else is very easy. 

  

Currently I have a patent pending on what seems to be a very exciting technology.  I have gained the attention of a few multi-billion dollar tech companies that are interested in purchasing the technology.  This is where I stand.  I have a wonderful wife that I've been married to for over 6 years, we have our first child on the way.   I cannot wait to be a father!  I may be selling my business in the realization of "The American Dream."  I have Aspergers. 

Thank you for taking the time to share and encourage families who feel overwhelmed and fear for the future of their Aspie child.

Truly a story of the hope and the "American Dream" .... You have overcome so many incredible challengenes, I salute your determination and logic.

Congratulations - what a wonderful father you will make!

 
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January 18, 2006, 3:47 pm PST

Trying Risperdal for AS son

Quote From: lainek

I have a 10 year old somewhere on the autistic spectrum.  I say somewhere because no professional since his age 2 has been willing to commit to a diagnosis.  He has always gotten services through school under an autism label although placement has always been a problem because he fits in neither the regular classroom nor the self-contained classroom.  What has ended up happening is that each year we get a different mix of how services are delivered to him. .. basically, he's "classless" and "peerless" at school.  Anyways, the specific reason I'm writing is because Risperdal has saved our lives in terms of his uncontrollable behavior and sleep problems.  With the Risperdal we've felt safer and he feels more in control.
I was reading the boards when I came across your message.  My son has been switched to Risperdal approx. 1 month ago.  My son has an EA and her son is on the same medication so she suggested I look into it.  They didn't really have a lot of information about children only adults.  I spoke with our Pediatrician and he said yes we will try it for a month.  He also suggested we take our son out of school a week before Christmas Break and let this medication work in a safe environment just in case of any side effects.  We began with 1 pill for 10 days then 2 pills a day.  The dosage is .25mg. but I find that his sleeping is still a great problem.  I have used Clonidine for sleeping in past but I was told this medication will help him sleep.  Well good thing he wasn't going to school because he was staying up until 11 and 12:00  at night.  And of course I can't go to sleep until I know he is sleeping so both of us where very tired.  Even in the morning he was up at 6 or 6:30 and of course so was I.  I checked with the Doctor and he said put him back on the Clonidine until I see him again.  We are scheduled for the 23rd of this month.  I'm still using the Clonidine for sleep because he needs sleep very much.  Now he is having stomach aches and headaches about going to school.  I don't believe it's the medication so I have arranged a meeting with both his teacher and his EA.  We have to get to the bottom of things before they turn out bad.  He believes that his teacher is yelling at him and he is afraid of her.  He says his friends aren't his friends anymore.  Sometimes I feel like I don't know what to do.  I know his fears are not unfounded but sometimes you have to dig deep to find the real reason.  I'm sorry I got off track with other issues.  I would like to hear more about any child out their on Risperdal.  Since we are so new to the medication I would like to hear from other parents using this medication.  And I know there are some people would don't believe in medication I have tried without and I was not helping my son at all.  He even asked me himself that he needed something to focus with.  As a parent this breaks your heart hearing your child asking for help.  Please don't feel guilty if that works for you who is anyone to decide.  If you would like to email me I would love to hear from you.  You can email me at lisa_phillips@sympatico.ca .  Just being in touch with someone going through the same thing just makes you feel better. 
 
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January 18, 2006, 3:49 pm PST

MAYBE I CAN GET SOME HELP FOR MY SON

I SAW THE SHOW ON THE 17TH AND I WAS RELEIVED TO HEAR THAT I AM NOT ALONE IN SEARCH FOR ANSWERS FOR MY SONS "TIC". 

WILLIAM (WE CALL HIM BILLY) IS AN ACTIVE 15 YEAR OLD IN HIGH SCHOOL WITH VERY GOOD GRADES. HE'S ACTIVE IN BASKETBALL, AND THAT IS HIS  PASSION.  ALTHOUGH, BECAUSE OF THESE TICS (HIS BLINKING EXCESSIVELY AND THROAT NOISES) HE DROPPED OUT, THE NIGHT OF TRYOUTS.  HE WON'T EVEN GO OUT WITH FRIENDS MUCH ANYMORE BECAUSE OF THIS. 

WE'VE BEEN TO THE NEUROLOGIST AND HE SAID HE THOUGHT MEDICATION WOULDN'T HELP BECAUSE IT WOULD TAKE HIS LUSTER FOR HIS GUITAR PLAYING AWAY. THAT'S ALL HE HAD TO SAY, BECAUSE WHEN BILLY PLAYS THE GUITAR IT RELAXES HIM.  HE HATES THAT HE HAS NO CONTROL OVER IT. HE'S RECENTLY MISSED SEVERAL DAYS OF SCHOOL BECAUSE OF THE INCREASED INTENSITY.  THE DR WOULDN'T GIVE HIM AN EXCUSE FOR SCHOOL, BECAUSE HE SAID TICS AREN'T SOMETHING TO MISS SCHOOL FROM. (EASY TO SAY, BUT TELL THAT TO A 15 YEAR OLD, WHOSE SOCIAL LIFE MEANS ALOT IN HIGH SCHOOL) 

I'M WONDERING WHAT TYPE OF MEDICATION HE'D BE ON AND WHAT THE SIDE EFFECTS WOULD BE.  HE DOESN'T YELL OUT OR SEEM TO HAVE TOURETTES, BUT HE TRIES TO SUPPRESS HIS EYES FROM BLINKING AND HE SAYS THAT'S WHY HE MAKES THROAT NOISES. 

MY HUSBAND AND I HAVE TRIED TO MAKE THINGS VERY CALM AND UNSTRESSFUL..BUT WE DO HAVE A 10 YEAR OLD THAT OFTEN WANTS TO SEE HIS "BIG" BROTHER IN HIS ROOM WHEN HE'S TRYING TO CONCENTRATE ON HOMEWORK OR PLAYI8NG HIS QUITAR. SO I KNOW THAT GETS HIM WORKED UP. WE TRY NOT TO FOCUS ON HIS PHYSICAL TICS, BUT LATELY HE PUTS HIS HEAD DOWN ALOT.  HE'S CARING, SINCERE AND HAS ALOT TO GIVE TO OUR SOCIETY I JUST WANT HIM TO LIVE A NORMAL LIFE. 

SLEEP SOMETIMES HELPS, BUT HE ALREADY GETS 9 HOURS , MORE ON WEEK-ENDS, AND THIS IS JUST GETTING WORSE. 

DOES ANYONE HAVE THIS PROBLEM AND CAN I GET SOME FEEDBACK? 

THANKS SO MUCH,  

A VERY WORRIED MOTHER 

 
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January 18, 2006, 4:04 pm PST

Billy

Quote From: kplewis

I SAW THE SHOW ON THE 17TH AND I WAS RELEIVED TO HEAR THAT I AM NOT ALONE IN SEARCH FOR ANSWERS FOR MY SONS "TIC". 

WILLIAM (WE CALL HIM BILLY) IS AN ACTIVE 15 YEAR OLD IN HIGH SCHOOL WITH VERY GOOD GRADES. HE'S ACTIVE IN BASKETBALL, AND THAT IS HIS  PASSION.  ALTHOUGH, BECAUSE OF THESE TICS (HIS BLINKING EXCESSIVELY AND THROAT NOISES) HE DROPPED OUT, THE NIGHT OF TRYOUTS.  HE WON'T EVEN GO OUT WITH FRIENDS MUCH ANYMORE BECAUSE OF THIS. 

WE'VE BEEN TO THE NEUROLOGIST AND HE SAID HE THOUGHT MEDICATION WOULDN'T HELP BECAUSE IT WOULD TAKE HIS LUSTER FOR HIS GUITAR PLAYING AWAY. THAT'S ALL HE HAD TO SAY, BECAUSE WHEN BILLY PLAYS THE GUITAR IT RELAXES HIM.  HE HATES THAT HE HAS NO CONTROL OVER IT. HE'S RECENTLY MISSED SEVERAL DAYS OF SCHOOL BECAUSE OF THE INCREASED INTENSITY.  THE DR WOULDN'T GIVE HIM AN EXCUSE FOR SCHOOL, BECAUSE HE SAID TICS AREN'T SOMETHING TO MISS SCHOOL FROM. (EASY TO SAY, BUT TELL THAT TO A 15 YEAR OLD, WHOSE SOCIAL LIFE MEANS ALOT IN HIGH SCHOOL) 

I'M WONDERING WHAT TYPE OF MEDICATION HE'D BE ON AND WHAT THE SIDE EFFECTS WOULD BE.  HE DOESN'T YELL OUT OR SEEM TO HAVE TOURETTES, BUT HE TRIES TO SUPPRESS HIS EYES FROM BLINKING AND HE SAYS THAT'S WHY HE MAKES THROAT NOISES. 

MY HUSBAND AND I HAVE TRIED TO MAKE THINGS VERY CALM AND UNSTRESSFUL..BUT WE DO HAVE A 10 YEAR OLD THAT OFTEN WANTS TO SEE HIS "BIG" BROTHER IN HIS ROOM WHEN HE'S TRYING TO CONCENTRATE ON HOMEWORK OR PLAYI8NG HIS QUITAR. SO I KNOW THAT GETS HIM WORKED UP. WE TRY NOT TO FOCUS ON HIS PHYSICAL TICS, BUT LATELY HE PUTS HIS HEAD DOWN ALOT.  HE'S CARING, SINCERE AND HAS ALOT TO GIVE TO OUR SOCIETY I JUST WANT HIM TO LIVE A NORMAL LIFE. 

SLEEP SOMETIMES HELPS, BUT HE ALREADY GETS 9 HOURS , MORE ON WEEK-ENDS, AND THIS IS JUST GETTING WORSE. 

DOES ANYONE HAVE THIS PROBLEM AND CAN I GET SOME FEEDBACK? 

THANKS SO MUCH,  

A VERY WORRIED MOTHER 

Maybe there are other meds that would be more appropriate for Billy's tics.   Get a second opinion.  Try going to a neurology department in a teaching hospital and get an evaluations, not just a neurologist in an office somewhere.   Maybe even one with a Developmental Pediatric department.  You will get more opinions because generally they use a "team" to diagnose.   Does he have an AS diagnosis?  Tics can come from a lot of things other than Tourettes - although you say he doesn't "seem" to have it - do you know for sure?  And the side effects would be different for the different meds, you would have to look those up once you have meds suggested to you.

There are also homeopathic therapies that can work, as well as diet.  Look online for "tics" and "Tourettes" with "holistic" or "homeopathic" and see what you find -
 

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January 18, 2006, 4:05 pm PST

meds don't work

Quote From: bunkie1326

I was reading the boards when I came across your message.  My son has been switched to Risperdal approx. 1 month ago.  My son has an EA and her son is on the same medication so she suggested I look into it.  They didn't really have a lot of information about children only adults.  I spoke with our Pediatrician and he said yes we will try it for a month.  He also suggested we take our son out of school a week before Christmas Break and let this medication work in a safe environment just in case of any side effects.  We began with 1 pill for 10 days then 2 pills a day.  The dosage is .25mg. but I find that his sleeping is still a great problem.  I have used Clonidine for sleeping in past but I was told this medication will help him sleep.  Well good thing he wasn't going to school because he was staying up until 11 and 12:00  at night.  And of course I can't go to sleep until I know he is sleeping so both of us where very tired.  Even in the morning he was up at 6 or 6:30 and of course so was I.  I checked with the Doctor and he said put him back on the Clonidine until I see him again.  We are scheduled for the 23rd of this month.  I'm still using the Clonidine for sleep because he needs sleep very much.  Now he is having stomach aches and headaches about going to school.  I don't believe it's the medication so I have arranged a meeting with both his teacher and his EA.  We have to get to the bottom of things before they turn out bad.  He believes that his teacher is yelling at him and he is afraid of her.  He says his friends aren't his friends anymore.  Sometimes I feel like I don't know what to do.  I know his fears are not unfounded but sometimes you have to dig deep to find the real reason.  I'm sorry I got off track with other issues.  I would like to hear more about any child out their on Risperdal.  Since we are so new to the medication I would like to hear from other parents using this medication.  And I know there are some people would don't believe in medication I have tried without and I was not helping my son at all.  He even asked me himself that he needed something to focus with.  As a parent this breaks your heart hearing your child asking for help.  Please don't feel guilty if that works for you who is anyone to decide.  If you would like to email me I would love to hear from you.  You can email me at lisa_phillips@sympatico.ca .  Just being in touch with someone going through the same thing just makes you feel better. 
my son has been on several different medications, including resperdol and clonidine.  They did not work.  Some may work, some won't.  But, don't depend on the false hope that there is a magic pill that help - most of it is behavior modification.  I urge everyone to find social skills training groups for children with AS.  Look on the websites for your county autism society.  They are out there, but you have to ask around.
 
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January 18, 2006, 4:06 pm PST

Asperger's, the good, the great and the wonderful

My 24 year old son was diagnosed with Asperger's when he was 20.  He was thrilled when he found out because it finally answered why he was different.  Throughout school he was provided with special ed due to learning disabilities and some of the other "symptoms."  He was treated for Aspergers without knowing it was Asperger's.  The treatment was the same.  Of all the many wonderful solutions to my son's problems, the one that made the most difference was enrolling him in a non-violent form of Martial Arts, which he practiced from age 9 to 21.  It taught him a great deal about self control and self esteem and discipline.   The early journey was not an easy one, but as we look back, we embrace and honor it.  We have sought resources through support groups; we have as a family learned to embrace the uniqueness that it has made our son.  And because of the genetic link to this, my son has formed a bond with family members  that might not have happened otherwise as he has opened doors to them as well.  There are plenty of resources out there on the web, many of them great.  Keep looking.  Keep positive.  My son is not living the life I initially dreamed for him.  But he's living his own, contented, and occasionally surprising us all when he ventures outside the box that could have kept him isolated.  I wish that everyone could have the wonderful sense of self that he has developed. 

 
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January 18, 2006, 4:06 pm PST

Great!

Quote From: paxmir

I don't know if we can post websites..i see so many doing so. 

Famous geniuses with Asperger's... 

http://www.geocities.com/WestHollywood/Stonewall/4502/famousac.html 

  

For a humourous fake diagnosis of socalled normal people Neurotypical shows the humour and wit of people with Asperger's. 

http://www.isnt.autistics.org/ 

  

  

What Is NT?

Neurotypical syndrome is a neurobiological disorder characterized by preoccupation with social concerns, delusions of superiority, and obsession with conformity. 

Neurotypical individuals often assume that their experience of the world is either the only one, or the only correct one. NTs find it difficult to be alone. NTs are often intolerant of seemingly minor differences in others. When in groups NTs are socially and behaviorally rigid, and frequently insist upon the performance of dysfunctional, destructive, and even impossible rituals as a way of maintaining group identity. NTs find it difficult to communicate directly, and have a much higher incidence of lying as compared to persons on the autistic spectrum. 

NT is believed to be genetic in origin. Autopsies have shown the brain of the neurotypical is typically smaller than that of an autistic individual and may have overdeveloped areas related to social behavior. 

  • The Diagnostic and Statistical Manual of Normal Disorders: 666.00 Neurotypic Disorder

Tragically, as many as 9625 out of every 10,000 individuals may be neurotypical. 

 
ROFL!!! That is priceless!!!
 
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January 18, 2006, 4:11 pm PST

Get a Second Opinion

Quote From: mikazuki

What's worse is you know something is wrong with your child so you take him from doctor to doctor and no one knows what’s wrong with your child. Teachers, doctors and speech pathologists know something is wrong but exactly what they have no idea.

My eldest son is four and will be five in May. He does not talk clearly and only in recent months has there been any improvement in his speech. He's not retarded or autistic, so the doctors and teachers say, but he has some kind of brain damage that has left him anything but a normal four-year-old boy. He's supposed to go to kindergarten this fall but I have heavy reservations about sending him since he cannot communicate with people. If you ask him his name instead of saying it, he will respond, "Eoohh".

He has had his hearing tested when he was younger and he's been tested for autism but the tests showed his hearing was fine and that he is not autistic. But what is he? What's wrong with him? Will he be subjected to special education for the rest of his time in school? And what do I do when he's older?

And what's even more worse, not having health insurance or more money to find a specialist that can determine what's wrong with your child. Heaven help those getting assistance from the state because more often then not you won't find help from a specialist because they are not taking new patients.
My son did these things.   "Eoohh" was really familiar in our house.  And he has AS.   What testing did your son have?   Is he in early intervention?  If he isn't, he should be!  You can call your county MHMR or ARC - even if he is not retarded, they can tell you where to call - and find out what agency you need to contact to get him started.  He needs to go to early intervention - they may want to delay kindergarten a year, or have another option for him until he's ready.

Get a second opinion.  Go to a Children's Hospital, and get a full evaluation on him, via a Developmental Pediatric department.  If you don't have insurance, some states do have Medicaid and other insurance for children and you should call the Department of Welfare, or whoever handles the insurance for your state.   Don't go for the "specialist" - go directly to the Children's Hospital.  They HAVE to take "new patients."

You want to have him get an ADOS and CARS test (also ADI if he hasn't had it).   That will tell you if he is on the autistic spectrum or not.  If you don't get the proper testing, you won't get the proper services. 
 
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January 18, 2006, 4:23 pm PST

AS Partners

Hi, 

I'm so grateful to the Dr. Phil show  for introducing Asperger's Syndrome.  It is a difficult topic to cover in such a short amount of time, but they were able to tell one family's story and open some minds to how difficult it is to live with this disorder. My husband has AS and I work with AS kids and their families.  Although the DSM-IV clearly delineates AS from Autism, individuals on the spectrum have some very unique needs. 

  

I hope Dr. Phil has considered doing a show on adults with AS.  It would be a great  follow-up to this last one.  Imagine being married to one of these guys.  Although the rage issue is somewhat atypical for AS, with or without the anger problems, it is a formidable task trying to make life... pleasant. 

  

For further study on how the spouses feel, click on
 
http://forums.delphiforums.com/ASPartners 


It is a great resource in discovering how neurotypical people feel when married to these folks. 


Thanks so much for reading, 

Nancy T 

 
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