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AS Symptoms (Full Official Criteria), test and some associated conditions info. Dyspraxia, bipolar + PDF Print E-mail
Written by AsPlanet.info - UPDATED July 2010   
Jul 11, 2007 at 04:20 AM
Aspergers Syndrome History and Symptoms 
"I offload to stop overload and as I have found understanding self fully takes time
and is a process. So finding out about things, for some of us I feel we should of been
told so long ago, at first a shock and then realization we are not who we thought as told!"
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We all should remember that everyone is born a unique individual and that those of us on the autism spectrum are as diverse and different as those that are not, there is no one list. Professionals often give us labels to try and understand, put us into tick boxes we may not quite fit into. So I feel it should be more about understanding, allowing and accepting self. The diagnostic criteria is a generalized "norm" and in fact we are all different, with different life experiences and that impacts on how we react to our own traits and who we are and whatever labels we are given "autistic, bipolar" they are simply words, as there is a real individual behind each diagnosis, we are all human..

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I also feel for far too long those not on the autism spectrum have often excluded us and written about us and they try and put us into boxes many of us will never fit into, we will never be a lists of differences, it’s a whole way of being. And of course we are as varied as those not on the spectrum, imagine trying to sum up non spectrum individuals with a simply list of criteria But hopefully some of the information below, will help you understand that little bit more, as a label does not define someone, but can help explain and help others understand, but often the start of a long process.(Alyson Bradley - May 2010)

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 Aspergers Officially Placed Inside Autism Spectrum

http://www.npr.org/templates/story/story.php?storyId=123527833

 

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Aspie Adult checklist (Alyson Bradley /  www.asplanet.info – Sept. 2008 / updated May 2009):

1. Over think, analyze things,2. Prefer own company, 3. Obsessional interest, 4. Like routine, 5. Like rituals, 6. Collections, 7. Sensory problems, 8. Over focus on details, 9. Perfectionist, 10. Think outside the box!, 11. Cannot understand jokes, 12. Weird laugh and/or make odd noises,13. Nervous fidget, Stim, 14. Upset by crowds, shy, 15. Face doesn't show emotion, 16. Very honest, can seem naïve, 17. Quirky, different somehow , 18. Cannot understand point of small talk, 19. Cannot understand society unwritten rules, 20. Bullied at school, work etc., 21. Lack of friends, socializing, 22. Friends much older or younger, 23. Mumbles, speaks to self, 24. Inappropriate emotions, response,  25. Connect well with animals, 26. Computer (Mr Spock) like logic, 27. Unexplained memory lapses, 28. Irregular sleeping patterns, 29. Hopeless or expert with maps, 30. Awkward, clumsy, bad body posture....

If most applies, do the AQ and AspieTests below:

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The AQ Test is not a means for making a diagnosis, however, and many who score above 32 and even meet the diagnostic criteria for mild autism or Aspergers report no difficulty functioning in their everyday lives. Asperger AQ Test http://aq.server8.org/

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and The Aspie Test: http://www.rdos.net/eng/Aspie-quiz.php
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Simon Baron-Cohen has argued that AS and high-functioning autism are different cognitive styles, not disabilities, and that a diagnosis of AS/HFA should not be received as a family tragedy, but as interesting information, such as learning that a child is left-handed. According to Baron-Cohen, "people with AS/HFA might not necessarily be disabled in an environment in which an exact mind, attracted to detecting small details, is an advantage. ttp://www.ncbi.nlm.nih.gov/pubmed/11014749
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"Tony Attwood argues, "the unusual profile of abilities that we define as Aspergers syndrome has probably been an important and valuable characteristic of our species throughout evolution." T. Attwood (2006). The Complete Guide to Aspergers Syndrome.
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Emerging%20Hills 
EMERGING 

A Bradley

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"It's not an easy journey at first to realize you are different
from the self you were stereo typed to be, but let me reassure
you that if you have Aspergers then you need to learn to
accept understand and allow your differences and be,
because only then will your unique brilliant shine trough..
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What is autism? - British Medical journal Group 
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  Is the autism spectrum too broad?

http://regulus2.azstarnet.com/blogs/puzzlepieces/16838/?

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 The Bipolar Timewarp - Do people cycle in
and out of time. "This is so like my own moods!"
http://www.youtube.com/watch?v=BM1CSqzQPq4
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- AsPlanet Forum discussions -
Coping with Depression. Advice & Support 

http://asplanet.info/forum/index.php?topic=1230.0

Co Morbid / Associated Learning Dificulties

http://asplanet.info/forum/index.php?board=10.0

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"Each one of us born a unique individual, each one of us has

our own unique story, each one of us has a reason and a right

to be who they were born as. So I wonder at times why so

many spend hours trying to label, trying to get to conform,

trying to fit into their stereo type world, maybe it's as simply

as stepping outside our own safe zones from time to time!"

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Sensory wise - overload, shutdown, meltdown, withdraw

 

 Many of us get a little lost for a while - Moods, bipolar etc...

http://asplanet.info/index.php?option=com_content&task=view&id=135&Itemid=181

 

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Report of the DSM-V Neuro-developmental Disorders work group - April.09

http://www.psych.org/MainMenu/Research/DSMIV/DSMV/DSMRevisionActivities/DSM-V

-Work-Group-Reports/Neurodevelopmental-Disorders-Work-Group-Report.aspx

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Well done team NZ ASD Guideline web site up and running : http://www.asdguideline.com/home?user_type=recognisers
 

This website contains guidance on recognition and referral of autism spectrum disorder (ASD) for people working in health, disability, education and community settings. ASD resources are drawn from the 'New Zealand Autism Spectrum Disorder Guideline' (April 2010)

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The DSM-IV criteria is continually being updated, changed

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The most recent complete release of the DSM, the DSM-IV, occurred in 1994. At this point, the category of pervasive developmental disorders and several subtypes were added. In addition to autistic disorder, a diagnosis could be made under the categories of Asperger’s Disorder, Rett’s Disorder, Childhood Disintegrative Disorder, and Pervasive Developmental Disorder Not Otherwise Specified (PDD-NOS).

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Besides the inclusion of four new subtypes, drastic changes were made to the criteria that needed to be met in order to receive a diagnosis of autistic disorder. The current release of the DSM has a list of 16 different symptoms used to describe autistic disorder and a patient only needs to exhibit six of the 16 to receive the diagnosis. This is in stark contrast to the language used in the 1980 release of the DSM-III.

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The DSM-V is currently in the works and there are large groups of individuals working on changing the language used to describe the various pervasive developmental disorders. Autism has evolved through the four releases of the DSM and it is only natural to expect that it will be refined even further in the DSM-V.

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DSM-IV (1994) and DSM-IVR (2000)

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Onset during infancy or early childhood 

Specify if childhood onset (after 36 months of age)

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299.00 Autistic Disorder

  1. (1)A total of six (or more) items from (1), (2), and (3), with at least two from 1, and one each from 2 and 3: 
  2. 1.  Qualitative impairment in social interaction, as manifested by at least two of the following:
  3. Marked impairment in the use of multiple nonverbal behaviors such as eye-to-eye gaze, facial expression, body postures, and gestures to regulate social interaction.
  4. Failure to develop peer relationships appropriate to developmental level.
  5. A lack of spontaneous seeking to share enjoyment, interests, or achievements with other people (e.g., by a lack of showing, bringing, or pointing out objects of interest).
  6. Lack of social or emotional reciprocity.
  7. 2.  Qualitative impairments in communication as manifested by at least one of the following:
  8. Delay in, or total lack of, the development of spoken language (not accompanied by an attempt to compensate through alternative modes of communication such as gesture or mime).
  9. In individuals with adequate speech, marked impairment in the ability to initiate or sustain a conversation with others.
  10. Stereotyped and repetitive use of language or idiosyncratic language.
  11. Lack of varied spontaneous make-believe play or social imitative play appropriate to developmental level
  12. 3.  Restricted, repetitive, and stereotyped patterns of behavior, interests, and activities, as manifested by at least of one of the following:
  13. Encompassing preoccupation with one or more stereotyped and restricted patterns of interest that is abnormal either in intensity or focus.
  14. Apparently inflexible adherence to specific, nonfunctional routines or rituals.
  15. Stereotyped and repetitive motor mannerisms (e.g. hand or finger flapping or twisting, or complex whole body movements.
  16. Persistent preoccupation with parts of objects.
  17. (2)  Delays or abnormal functioning in at least one of the following areas, with onset prior to age 3 years: 1 social interaction,() language as used in social communication, or 3 symbolic or imaginative play.
  18. (3)  The disturbance is not better accounted for by Rett's disorder or childhood disintegrative disorder.
©2007 Roy Richard Grinker

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See Diagnostic Criteria for Autistic Disorder through the years,
for more indepth info - Unstrange Minds:  http://www.unstrange.com/dsm1.html
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NEUROLOGICALLY COMPLEX - Aspergers Dyspraxia, Dyslexia, ADHD, Bipolar etc...

Join us on AsPlanet forum where many similar discussions :

http://asplanet.info/forum/index.php?topic=1465.msg15891#msg15891

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Autism's False Prophets

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What is Asperger syndrome? Asperger syndrome is a form of autism, a

condition that affects the way person communicates and relates to others.

People with Asperger syndrome may find difficulty in social relationships and

in communicating, and limitations in social imagination and creative play.

The National Autistic Society - Mental health and Asperger syndrome:
http://www.nas.org.uk/nas/jsp/polopoly.jsp?d=128&a=3346

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"Do people flap on the autism spectrum I was asked, my answer in varied ways, usually

a stress release... and yes some of us with aspergers do also. Just like anyone as we grow

up, we learn to adapt/ change and so often if we do as a child it's less obvious as an adult,

or we just do not do in front of others....But flapping can just be shaking hands with

excitement "overloading", the description below is as good as any: Stimming is a jargon

term for a particular form of stereotype, a repetitive body movement (often done unconsciously)

that self-stimulates one or more senses in a regulated manner. It is shorthand for self-

stimulation, and a stereotypy is referred to as stimming under the hypothesis that it has a

function related to sensory input. [1] Stereotypy is one of the symptoms listed by the

DSM IVfor autism http://en.wikipedia.org/wiki/Stimming

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Dyspraxia
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I have heard it said that maybe everyone with asd has a little dyspraxia, or is it all those with dyspraxia have Aspergers - just some think I heard, so please do not quote me on this, but many neurological differences seem to overlap and interact, the "fruit salad mix" as Donna Williams calls it, it seems the problem is often working out what we do and do not have, getting a correct diagnosis for all our differences often chaotic and disjointed, dyspraxia really simply another piece of the puzzel for me!
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DRIVING as people keep asking me about this, decided to add para.
"I have so many stories on this, the first time I attempted to drive a car,  I drove the wrong direction - over the pavement, I tended to drive to where ever I was distracted, looked and usually all over the place, as it is extremely hard for me focus my thoughts on a task when my mind over active and often full of other exciting thoughts!"
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While many do drive and very well it depends on many things. Myself even though passed my first test, as tend to be able to do anything I put my mind to, but as with most things learned in my own way, do things in my own way and so fitting in on the road never quite worked for various reasons, lack of support at the time, funds to have enough lessons, lack of confidence, never needed to as grew up in London, too much inter action with others, too many detractions for me..and when I was learning no one understood my differences, including, me at the time...
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But with the right support I feel I would be driving now and wished still at times I followed through and could, in theory I have a license, but would need a lot more lessons before driving again. It may take a little longer to get there, but truly worth it, age or our differences should not hold us back, its often lack of support or understanding from others that stops many, frustrating not being able to do like others and often not being heard! 

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Having dyspraxia and other neurological complexities for me means "To be able to steer a car, concentrate, and judge distance, use both hands and feet together and remember how to carry out a sequence of tasks all at the same time is very daunting...." See Dyspraxia Foundation - Driving: http://www.dyspraxiafoundation.org.uk/services/ad_driving.php

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But I guess I have quite a few associated conditions dyslexia just another one from my list... so it really also depends on your associated, co morbid conditions. I do feel the younger we learn the easier, it may take longer but we are very capable. There are some people who now specialize in dyspraxia, neurological different drivers, generally slowly worldwide becoming more recognized... in the UK the dyspraxia foundation will be able to advise. 

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It is advised that all asd people should also have special eye sight tests or at least advise the optometrist your on the autism spectrum and let them know you want to drive as they can pass you. I had many sight problems and my sight was not good enough to drive anyway for part of my life, but even without sight problems many of us on the autism spectrum have peripheral vision problems, I tend to sense more than see in these areas and that can be a real problem for me driving... 

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LEARNING IN A AUTOMATIC CAR helps a lot, and is often

advised,  less distractions, the gears was/is what I found

so hard, too much for me to concentrate on all at once.  

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DRIVING and DYSLEXIA / DYSPRAXIA and more come chat on

AsPlanet Forum :: http://asplanet.info/forum/index.php?topic=5.0

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I do wonder if partly my problem is that cars do not fascinate

me, well not an obsessive interest, to me just plain cold mental a

functional use to get from A to B no wonder find hard to focus,

when so many other real wonders surrounding us in the world, I

would rather look than drive and so guess this quote kind of sums

things up for me:  "I know a lot about cars. I can look at a car's

headlights and tell you exactly which way it's coming." - Mitch Hedberg

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Aspergers diagnosed/undiagnosed! later in life etc...

 http://asplanet.info/forum/index.php?topic=32.0

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 Basic History and Symptoms 
(Full ASD Official Criteria see below)
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The Cause of Aspergers Syndrome is unknown; there may be a genetic component to this syndrome. Aspergers syndrome, also known as Aspergers disorder or AS, is a pervasive developmental disorder (a spectrum of behavioral disorders including autism) Aspergers syndrome is characterized by an inability to understand how to interact socially and a pattern of repetitive behaviors and/or restricted interests. Unlike persons with autism, those with Aspergers syndrome do not show a marked delay in language development or cognitive development.

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Aspergers Syndrome, was first identified as a unique medical condition in 1944. Prior to this time, the disorder was probably misdiagnosed as another behavior disorder or simply not diagnosed at all.

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An Austrian pediatrician name Hans Aspergers named the disease after noting its presence in four of his male children patients. He called it, at the time, "autistic psychopath." He noted that his young patients seemed intelligent and had regular speech development, but simply could not communicate because they could not understand non-verbal cues. Unfortunately, no more research was done on this condition, as Aspergers did not place a high importance on it.

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It was not until 1981, almost 40 years late, when English doctor Lorna Wing, continued the study of AS. She was the first to call it Aspergers Syndrome, and her studies are famous in the AS world even today. Even with the research Wing was doing in the medical community, the stir she was causing about this condition did not convince the World Health Organization to recognize the condition until 1992.

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It was included as a disorder in the organization's tenth edition of their diagnostic manual as well as in the International Classification of Diseases of that year. However, it wasn't until two years later, in 1994, that AS was a separate disorder according to the Diagnostic and Statistical Manual of Mental Disorders.

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Aspergers syndrome is commonly recognized in children after the age of 3 years and is more frequently diagnosed in boys. Children with Aspergers Syndrome are typically educated in the mainstream but usually require special education services. These children often have difficulty making friends, and are often bullied or teased by their peers.

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An individual's symptoms can range from mild to severe. May have all or only some of the described characteristics, and they may exhibit more problems in unstructured social settings or new situations that involve social problem-solving skills. Individuals with Aspergers syndrome have serious impairments in their social and communication skills, including poor nonverbal communication. However, many individuals have good cognitive and verbal skills, and typically have normal to superior intelligence. Many have excellent rote memory and become intensely interested in one or two subjects.

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Lorna Wing Quote:
"What we want to know is what makes this person tick in the way they are ticking? It's fascinating disentangling; its a piece of detective work, how this person has reached this point.
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It seems to us from our experience that it is far more important than deciding whether or not someone fits the classic criteria. We have come across a lot of people who don't fit any of the classic criteria, but deep down they actually have poor development of their social understanding and their capacity for planning. These two things (they may not have anything else) in life are going to be hellishly difficult for them, and they're going to get into all kinds of silly situations and terrible trouble, even legal trouble as a result. This to us is what matters."

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I come from one of those families who "have poor development of their social understanding and their capacity for planning." We also have members who could have/had a diagnosis of Asperger's. But because most of us have fairly normal communication, the overt difficulty is mostly hidden - until we become overwhelmed by trying to figure out how to relate to others, or make decisions, or deal with inevitable emotional stress. There is enough anxiety, depression, and suicide in my family, as a result of having a lack of social and emotional understanding, that I can attest the not-fitting-the-diagnostic-criteria end of the spectrum has it's share of human tragedy and need for understanding, too. "

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Lora Wing full interview by Autism Connect:

http://www.autismconnect.org/core_files/interviews/transcripts/lorna_wing.htm

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Desolate%20copy

DESOLATE
So powerful and strong, drawing you

into its own enchanting world - A Bradley

 

 

Social problems: Although children may express an interest in friendships, they have difficulty in making friends and may be rejected by peers; often these children are loving and affectionate with their immediate family. Socially inappropriate behavior, lack of understanding social cues, difficulty judging personal space, difficulty understanding others’ feelings and rigid social behavior due to an inability to spontaneously adapt to variations in social situations.

 

Abnormal communication patterns: Awkward or inappropriate body language, including limited use of gestures and absent or inappropriate facial expressions. Unusual, formal style of speaking, difficulty understanding non literal and implied communication. Impairments in the modulation of volume, intonation, inflection, rate, and rhythm of speech, speech may be tangential and circumstantial, often with irrelevant comments. Conversation style characterized by marked wordiness. Difficulty with “give and take” of conversation and lack of sensitivity about interrupting others.

 

Activities: Intense interest in a particular, often very restricted, subject that dominates the individual’s attention. Inflexible adherence to routines; has repetitive routines or rituals, and apprehensive about change, may have difficulty transitioning from one activity to another.

 

Sensory sensitivity: Sensitivity to sound, touch, taste, light, sight, smell, pain, and/or temperature and, sensitivity to the texture of foods.

 

Motor skill delays: History of delayed development of motor skills. Visible clumsiness and poor coordination and deficits in visual-motor and visual-perceptual skills, including problems with balance, manual dexterity, handwriting, rapid movements, rhythm, and imitation of movements.

 

 

 

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A Bradley

 

 

 

 

Official Criteria for Asperger Syndrome

 

The official diagnostic criteria for Asperger Syndrome are found in the Diagnostic and Statistical Manual of Mental Disorders, Text Revised DSM-IVTR (2000) published by the American Psychiatric Association. The DSM-IVTR is the major diagnostic classification reference for psychologists and medical professionals. Prior to its first inclusion in the 1994 version, Asperger Syndrome was not included in the DSM. Readers can find the original descriptive language under classification 299.80, Pervasive Developmental Disorders.

The summary listed below was taken from Pediatric Neurology (http://www.pediatricneurology.com/autism.htm#Asperger’s Syndrome). It reads in a rather stilted way, but that is a common complaint about the entire DSM-IV.

(A) Qualitative impairment in social interaction, as manifested by at least two of the following:
1. marked impairment in the use of multiple nonverbal behaviors such as eye-to-eye gaze, facial expression, body postures, and gestures to regulate social interaction
2. failure to develop peer relationships appropriate to developmental level
3. a lack of spontaneous seeking to share enjoyment, interests, or achievements with other people (e.g., by a lack of showing, bringing, or pointing out objects of interest to other people)
4. lack of social or emotional reciprocity.

(B) Restricted repetitive and stereotyped patterns of behavior, interests, and activities, as manifested by at least one of the following:
1. encompassing preoccupation with one or more stereotyped and restricted patterns of interest that is abnormal either in intensity or focus
2. apparently inflexible adherences to specific, non-functional routines or rituals
3. stereotyped and repetitive motor mannerisms (e.g., hand or finger flapping or twisting, or complex whole-body movements)
4. persistent preoccupation with parts of objects

(C) The disturbance causes clinically significant impairment in social, occupational, or other important areas of functioning.

(D) There is no clinically significant general delay in language (e.g., single words used by age 2 years, communicative phrases used by age 3 years)

(E) There is no clinically significant delay in cognitive development or in the development of age-appropriate self-help skills, adaptive behavior (other than in social interaction), and curiosity about the environment in childhood.

Basic Characteristics
The characterization of Asperger Syndrome above provides the reader with an "official view" of AS characteristics. However, among many clinicians who have seen vast numbers of autistic individuals since 1994, there is strong disagreement about the accuracy of the DSM-IV criteria. The 1994 criteria were developed after study of a relatively small number of persons. Since then, much more has been discovered about AS. Experienced child and adult diagnosticians have discovered that the official criteria are factually wrong on several critical areas; they also fail to account for many individuals seen in clinical and natural settings who exhibit classical autistic symptoms but develop speech late and demonstrate substantial deficient cognitive functioning and faulty perceptual awareness of others at an early age. There is strong pressure now being exerted on the editorial board of the DSM-V -- scheduled for publication in late 2005 or early 2006 -- to revise the criteria to better suit what sensitive diagnosticians have found to be true with thousands of late-diagnosed children and adults.

Since 1994, ethically responsible diagnosticians have adopted the view that autism is a spectrum disorder. Individuals diagnosed with Autistic Spectrum Disorder (ASD) occupy positions from one extreme end of autistic functioning continuum to the other.

To reflect current professionals' thinking about ASD's, the following section is a more accurate depiction of AS. Symptoms of AS include: impaired ability to utilize social cues such as body language, understand irony, or other “subtexts” of communication; restricted eye contact and odd, failed efforts at socialization; a marked and limited range of encyclopedic interests; perseverative, odd behaviors; didactic speech, verbosity, substantial problems with prosody, with voice tone regulation (monotone, droning voice); “concrete” thought accompanied with black and white dichotomous thinking; hyper and hyposensitivity to sensory stimuli; and unusual body awareness and movement.

For ease of discussion and reading, the term "he" is used in this article to refer generically to both AS males and females. In the writing below, where there is differentiation in responses or characteristics between the sexes, it will be noted separately.

Uta Frith, the English clinician who first translated Hans Asperger's 1944 German language paper into English in 1991, suggests that there are five main characteristics that identify AS:

(1) impaired social relationships
(2) impaired communication
(3) impaired make-believe play
(4) a peculiar pattern of intellectual abilities, and
(5) the repetitive phenomena of rituals

By analyzing each of these characteristics the reader can better understand how AS is identified. In the material below, a variety of symptoms associated with AS are discussed. Not every characteristic manifests the same way in each individual. What makes AS a syndrome as opposed to a singular description of a specific disabling condition is that its symptoms appear with high frequency within the same individual, in "clusters" as opposed to individually identifiable features, and with great consistency at any given stage of the individual's development. For this reason, it is classified in the DSM-IV as a pervasive developmental disorder.

When first being diagnosed, whether as children or adults, clinicians familiar with differential diagnosis best assess individuals. Individuals diagnosed with AS often have other mental or physical health conditions, which combined with autistic traits, limit their ability to function. Individuals diagnosed as being "on" the autistic spectrum -- a continuum that ranges all the way from extremely low functioning individuals to those whose intellect is high -- are identified as autistic precisely because they are unable to function at critical levels of child or adult cognitive, social and communicative activity.

Impaired Social Relationships
As an AS child approaches school and has opportunity to be with his non-autistic peers, his social and communication challenges become noticeable. Invariably the AS child remains off by himself rather than being actively engaged with other children. Even when with a group of children, AS children operate on what appears to be a parallel track. At this stage of social development, observers note that the AS child is a “loner. Found in their remarks may be terms phrases describing the child as "in a world of his own”.

AS children may desperately want to have friends, but without formal and patient training they are unaware of how to initiate contact with others in order to move on to forming the friendship bond appropriate for "normal" persons their same age. When asked about their friends at each developmental stage where friendship is described by "normal" children in increasingly sophisticated terms, AS children describe friendship in ways quite differently than their peers. While many AS adolescents state they have a number of friends, upon closer examination their "friends" are more accurately described as acquaintances, or even individuals they see casually or once. By the time AS children reach adulthood, they have learned to be either direct in their statement that they have few or no friends, or be evasive and circumspect with their answers. Without careful prodding and determining what the AS adult "means" when describing their friendships, many diagnosticians miss critical information that would otherwise inform them that the AS adult's notion of friendship is both developmentally delayed and distorted from the ordinary meaning of the term "friend".

Without deliberate, patient instruction about the meaning of relationships, friendship, and sexual bonding, many individuals with AS remain adrift on a sea of confusion with unanswered questions about "why" they continue to have difficulty forming such relationships. Even as an adult, without proper training the AS individual may easily make "first base" acquaintanceships, but lack the expertise to change those relationships into adult friendship, a social date, or a successful spousal relationship.

Most AS individuals report being victims of childhood bullying, victimization, abuse, and teasing that they continue to fear in adulthood. Individuals not accurately diagnosed as autistic in childhood and adulthood are often abused and misunderstood within their own families, the one "last, safe refuge" of children and adults. As a result of their negative social conditioning, AS children and adults avoid strangers out of fear that earlier patterns of abuse will continue. Given ideal child-rearing conditions, even if they weren't actively abused, AS children and adults still feel misunderstood, and they often are. Out of fear of making mistakes, of being misunderstood, AS adults carry socially avoidant and distancing behavior into their hesitancy to initiate social communication and activities throughout their lives.

AS individuals appear naive and gullible to others. Studies of bullying and child abuse at the hands of non-family members show that individuals who are isolated or alone are perfect victims. They are targets for such behavior because they stand out from their contemporaries as odd, not being able to understand simple social cues and unwritten rules of social communication and the hidden or "other" meaning of words, phrases, or the facial and body gestures of others. Many AS individuals do not understand the significance of variations in vocal pitch, pauses, and expectations by others that they "keep up their end of the conversation". In addition they suffer the consequences of remaining on the outside or at the edge of social conversation and the social behavior of their non-autistic peers.

Anger, Frustration, and Dealing with Difficult Emotions
There are two common responses to thoughts and feelings of being misunderstood. One response is aggression; the other is passivity. While both responses may be present to some degree in the same AS individual, professional literature identifies at least these two phenotypes: dominant, aggressive, and controlling; passive, submissive yet controlling in more subtle ways. Throughout their lives, individuals maintain the same type of response to stress and frustration.

With both types of responses, there are common clinical conditions that accompany the AS diagnosis: depression and anxiety.

Aggression and "Behavior Problems"
In their effort to be accepted by people they do not understand, AS individuals may mimic the behavior and language of groups they hope will accept them. This tactic rarely works. They fail to understand the subtle aspects of language and non-verbal communication between members of these groups. If such groups engage in anti-social behavior, they often leave the AS individual "holding the bag". While their savvy acquaintances escape notice through denial or "acting normal", AS individuals temporarily abandoned by their cohort become "discipline" and "behavioral problems" for educators and other care providers.

Without painstaking training and repetitive opportunity to practice newly learned communication and social skills, AS persons will not, on their own, develop an intuitive understanding of social etiquette. Some AS individuals may become overbearing, domineering, bullying and controlling as a means of remaining in charge of their environment. This is far more common with boys than with girls, however cruelty and aggressiveness in AS women has been recently studied and found to be even more severe than that of their aggressive male counterparts (Aston, 2003). The domineering AS adult may demonstrate no sympathy for others, and show no remorse for any pain or suffering they inflict. This person does not understand that others have different expectations or “rules” of their own. Anger, frustration, and rage that an AS individual experiences may lead him to overstep the lines of decency, and move into outright psychological abuse, violence, and illegal activity. It is essential to the child's well being as an adult to work early and intensively to thwart this side of AS before it becomes ingrained into his personality.

Because of the rigid logic and limited cognitive flexibility of autistic persons with uncorrected behavior and attitudes, once an AS child becomes an adult, it is very difficult to "turn the behavior or attitude around". This feature of rigidity, of "hard wiring of responses" is as true for persons who are passive as those who are aggressive in their response to being misunderstood. Most AS adults who have chronic negative attitudinal or behavioral responses do not benefit from standard counseling or behavioral therapy. Only in the last several years have techniques been developed -- modifications of cognitive-behavioral therapy -- which have proven effective.

However, it is important to remember that such therapy works if and only if the AS individual accepts his Asperger Syndrome diagnosis, takes active steps to understand his own particular "flavor" of the condition and is willing to change and improve his conduct through a very painstaking and slow process inherent in such work. Even if the individual expresses a desire to change, the psychological cost may simply be too great. They and others in their lives may conclude that it is easier for others to make adjustments to their new understanding of the AS individual than to expect the AS individual to change, even though, logically, such change on their part makes perfect sense.

Most medical insurance programs will not cover the cost of such work, even if available through a small handful of trained professionals. At this time, school and public mental health programs offer no such counseling capacity.

Passivity, Non-Responsiveness and Anger
The second response to being misunderstood is social avoidance and passivity. This, too, is a life-long response.

AS children and adults can become submissive and cautious in their actions. They may show considerable empathy for others, and repeatedly apologize for their actions. In most cases, however, they continue to repeat the same conduct or behavior because they know of no other alternative, all the while knowing that at its conclusion they will engage in an inevitable round of apologies. With their aggressive counterparts, they develop a hypersensitive sense of justice and fairness. As with their their aggressive AS counterparts, they are unsure how to respond to others in order to develop friendships and normal social relationships. Their response is anger turned inward. Professionals reporting on these children find levels of self-injurious behavior that are above average. Self-injurious behavior and serious thoughts and attempts at suicide often result in these children being prescribed heavy dosages of anti-depressive and mood-regulating medications. A small but significant minority of children are "frequent flyers" in psychiatric emergency facilities, and some have long histories of hospitalization and institutionalization.

Quiet AS adults describe being overcome with rage—they feel as if something is taking over their body—they cannot control it. In deeply private moments when they are sure they aren't observed, they may let their rage go, screaming, destroying objects (often the same type of object time after time) until the rage subsides. Like their aggressive counterparts, they feel that once dissipated, they can "go on." In their case, this may be possible because no one has witnessed their volcanic explosion. Instead of stifling their emotions, these adults may express a desire to be happier by learning how to safely express their feelings in socially acceptable ways.

In the case of their "aggressive" counterparts, there is a similar feeling that once they are finished with their tantrum, nothing further should be made of their behavior. Such expectations are totally out of sync with others' expectations about how the individual should make amends for a recent explosive outburst. Even though their outbursts and controlling nature are right at the surface, individuals prone to explosive rage rarely acknowledge their feeling state. It is equally difficult for them to perceive the effect of their conduct on others.

Both aggressive and passive AS individuals tend to blame others for things leading up to their own explosions. While in the midst of a stressful event, they do not accurately perceive their contribution to an escalating situation. With aggressive individuals disinterested in changing their responses to frustration and anger, there may be little choice for others involved with them other than to physically leave the scene or the relationship. Passive individuals may be similarly inclined to feel that they can't change, but there is a greater likelihood that because much of their response to anger and frustration has been "private" others in their lives are willing to tolerate their passivity and non-responsiveness and accept the notion that they are unlikely to change. Such individuals may rely on others to perform many executive functions for them, such as time management, financial management, or short-term and long-term activities that require complex planning. Passive AS adults can be charming and attractive, especially to others who consider themselves helpers. Once married or after settling into a relationship, the AS adult's dependence becomes obvious, often earlier to others than their own partners. With an understanding of AS by their partners and others, people who consider themselves helpers or rescuers can make more informed decisions about whether they wish to maintain such a relationships. Often, they do.

Navigating the Social Mine Field
Individuals with AS cannot quickly study situations to decide on a socially appropriate course of action. Instead of having learned communication and social skills by intuition -- the process used by non-autistic children and adults -- they rely on a different process. In their writings and self-descriptions, many AS individuals describe how they make social decisions. They draw upon an experience-based knowledge base. Adults describe this knowledge base as working exactly like a computerized data bank. Asperger Syndrome individuals use this vast storehouse of knowledge to compare their perception of a current situation with ones experienced in the past.

Users of computerized data banks understand the concept of "Garbage In/Garbage Out." Asperger Syndrome individuals are notoriously inefficient organizers of information. Asked about a present situation, their perception of a given situation and its important noteworthy issues is highly idiosyncratic. Invariably, it is" I-centered". Their associations between past perceptions and their categories of response "folders" are likely to be wrong at the time they were first formed, and even more out of sync with a current event they find themselves in. Through life-long experience, they know this to be the case. Given time and enough "similar events", they eventually identify situationally appropriate responses, but the mental energy and processing time expended in finding the right words or the right behavior is enormous. When they are in a secure or stable adult relationship, their more functional partner often acts as a social go-between or interpreter of the social world for the AS partner. AS adults' dependence on their higher functioning partner is often characterized by their partner as "childlike" or even "like having another child in the household".

In all instances where AS individuals find themselves in different or unstructured social settings, they must take extra time to cognitively process their experience before responding. Others do not realize that this “processing time" is needed by the AS person to make sense of "new data". They tend to become aggravated at the slow or delayed pace of the AS person's reactions.

Exasperation and irritation of others "waiting" for a response, or realizing that the time it takes for an autistic person to respond at all is too long often leads to social rejection. Without being able to precisely name the cause -- but knowing that something "just isn't right" with the AS individual -- others respond as they often do when they don't understand strangers who act differently than themselves. Social rejection and other adverse reactions by others is a frequent cause for school drop out in AS child and adult students, termination of employment, or frequent physical changes in the AS individual's living arrangements. Indecision stemming from a real fear of making a mistake often leaves an AS person "spinning his wheels and getting nowhere". Equally distressing to others experiencing an AS person's inefficient problem solving is the AS person's repeated reliance on solutions or techniques they may once have found helpful but that don't work well any more.

In the case of children and adolescents, early and consistent formal training through role playing, guided instruction in social skills through the use of other socially savvy children and adults, Social Stories?, and the sensitive use of modified cognitive behavioral techniques can make a difference in an AS person’s understanding of how to form and sustain lasting relationships. (Attwood 2003)

For all such formal instruction, the AS individual must have safe opportunities to practice newly learned skills with another person in a supportive and respectful one-to-one setting. From that level, they can move into supportive small group settings, testing and generalizing social and thinking skills "scripts" into structured educational, social, community and work environments. (Winner, 2001; Gutstein 2002) As they experience success, many AS individuals can generalize those skills with strangers in the world at large. With rare exceptions, public school systems are unprepared for the cost and time involved in this type of social skills coaching. Because of the intensity of intervention required to work permanent results, parents of AS children spend thousands of dollars for private social skills training for their children.

For AS adults, almost nothing is known about effective treatment to obtain a similar "turnaround". For one thing, money and research time is not focused on adults; it is focused exclusively on children. Second, even for techniques that show promise with adults, formally conducted sessions by speech/language pathologists and specially trained psychologists have seen only mixed results. Third, in all cases with adults remedial work is extremely expensive and time-consuming and not covered by insurance or health care programs. For the present, AS adults' participation in support groups skillfully facilitated by other AS adults with AS appears to be one effective way that AS adults can learn to become comfortable with themselves, and, as they report, increasingly comfortable with others not on the autistic spectrum.

Impaired Communication

Impaired Theory of Mind combined with Processing Delays
From research in the early 1980's has come the term "mind blindness" and "failure of Theory of Mind" describing autistic individuals' difficulty in perceiving and understanding the intentions of others. AS is characterized by rigidity of thought, black and white thinking, and impulsive behavior (or its opposite - indecision). AS individuals tend to take everything literally, understanding everything said to them just the way they hear it spoken. Their hearing is "often wrong". When put the test, many AS children and adults demonstrate little true understanding of language pragmatics or how given words or a phrases' use changes depending upon an ever-shifting context. They do not intuitively understand hidden ideas, idioms, and double meanings. When informed about these social language short cuts, some AS individuals become sullen, angry, or withdrawn when in the presence of people using these conventions of speech. Others become "students of the hidden language", going to great lengths to catalogue this information in their data banks.

Even if an AS person masters the words, he will have difficulty understanding the meaning of non-verbal methods of communication (posture, gestures, nods, winks, or minute but detectable changes in facial expressions). Even if an AS individual gets the meaning right, additional problems with language pragmatics (proper use; proper context) and delays in processing auditory information means that he experiences difficulties keeping up with rapid receptive speech (spoken and nonverbal). The result is that the AS individual often feels left behind in ordinary conversation.

Savvy AS adults can develop sophisticated language and behavioral responses to new situations (Shore, 2003). Their mastery of listening and "sounding as if" skills is akin to mimicry. Even so, they operate within a very tight envelope. When pressed, many bright AS adults cannot further demonstrate an understanding of complex concepts or complex behaviors that have additional meanings. Many AS individuals who depend upon their verbal fluency know how to "fake it" or "pass as normal". (Willey, 1999) This coping behavior may get them by for a while. However, their oddness and slow processing eventually becomes known to others who interact with them frequently. Depending on the social context, others can adjust to their communication impediments because of the value of their contribution to a given enterprise or project.

Unusual Speech
Many AS children and adults develop a style of expression characterized by long, fact-filled monologues. They show an apparent disinterest about engaging other children or adults in a reciprocal exchange of conversation. They talk "to" individuals rather than "with" them. Some AS adults describe this speech process as a "data dump". They report that once started with a monologue, they find it difficult to stop. Much to the irritation of their age mates as well as adults, they also find comfort in repeating the same routine ad nauseum.

Asperger Syndrome children characteristically develop an erudite mastery of a special topic that may be of initial interest to their age mates, but just as likely not. AS individuals have a poor understanding of the visual and gestural non-verbal signs of listener boredom. Wrapped up in their monologue, when told to cut their presentation short, they may not hear an adult or another child asking them to stop or switch topics. Unless they've been repeatedly coached and have good self-monitoring skills, AS individuals don't understand polite but indirect hints to stop. Vague or non-concrete hints don't work either. Children are often direct and brutal when they correct one another. They leave or shun their motor-mouthed age mates.

Adults offer acceptance not available from their age peers. AS children seek out adults who indulge them out of true curiosity and amazement at their knowledge. Adults are socialized to be polite and subtle when dealing with people who run on. With their patience taxed to the breaking point, adult listeners often become exhausted, exasperated and bored. They can extricate themselves from uncomfortable situations because, as adults they have more power to control time and place.

Listeners wonder why AS individuals continually return the conversation to their favorite interest no matter how far the conversation has progressed into new topics. Sometimes this is because the AS person has mastered a script to tell a long story. He will turn to exactly the same choice of words and order of events as the last time the story was told. Some AS individuals react to interruptions to their monologues by starting them over again. Until they feel completed with their presentation, it is often impossible to have them move on in a conversation without their appearing irritated or even rude. The same need to start all over again when interrupted in a task impacts AS children and adults alike.

Oddly constricted special interests of AS individuals may be very difficult for listeners to deal with. As an example, a child that knows the manufacturing process of every toilet in Central Oregon may at first be interesting, but will bore others after an hour or two if they are even still listening and have not walked away.

Some AS individuals maintain the same interest in a given topic throughout their lives, while others move from one intense interest to another, often returning to earlier ones at later times in their lives. (Shore, 2003). If their special interest fits into the fold of general adult interests such as sports, entertainment or electronics, it is easier for them to make connections with like-minded individuals. AS individuals frequently put much effort into finding "targets" for their monologues by hanging around locations where such interests are common. While their knowledge still remains erudite, AS individuals can form intense, interest-based relationships with other adults. Adults who succeed in forming these relationships can gradually "catch the cues" of others. True adult friendship can arise from such relationships, but with a difference: the enjoyment an AS adult expresses when describing these relationships is often described in intellectual terms rather than emotional ones. Regardless of the terms they use, these relationships do have a substantial emotional component to them.

Expressive Speech Issues

Individuals with AS are often unaware of how their words and non-verbal signals "sound" to others. They may speak with loud, authoritative, monotone voices, droning on and on. Others, especially AS women, retain a small-person, child-like prosody and pitch to their voices, causing listeners to strain to hear them. Other AS individuals have normal adult speech, but they may be exceedingly quiet, limiting their contributions in conversations to a few words. They may go for hours at a stretch without saying anything. The AS person is quite unaware of the unintentional messages their style of speech sends to listeners. Many AS individuals do not know how to send the small postural, gestural, or vocal signals indicating they are still tracking what others are saying. When asked, AS individuals will say that they see no need to do that. They expect their mere presence to be enough of a signal to others that they are listening. They are unskilled in the art of repairing communication that has run off track or has "misfired". Based on voice tone, volume and postures that send a different message, listeners may conclude that the person is disinterested, angry, or hasn't heard them.

Employment problems of adults are often traceable to their poor social and communication skills. They may have some awareness that others are confused by or displeased with them, but don't have the social skills or conversational tools to find out why and correct their conduct. When asked about repeated instances involving the same faux pas, they cannot "connect the dots" or divine patterns in their own social conduct or speech responsible for their dilemma. By the time they realize they are making mistakes -- often in the midst of a string of behavioral and language-choice errors -- it is often too late for them to repair a deteriorated relationship. If the AS adult is lucky to have other adults available to help them unravel a confusing situation, the individual may learn how to sense danger signals and self-monitor his conduct before things reach a point of no return. Many AS adults reporting success and a tolerable level of social comfort later on in life can identify others in their lives who have acted as personal coaches or patient adult-skills instructors.

Stilted Speech
Highly verbal AS individuals tend to use more advanced vocabulary and grammar when simple words and simple syntax are called for. Their speech sounds stilted and "professorish". If they are fluent writers, they tend to write in an overly complex way. How much they say and write is related to their personal interest in a topic. An AS individual has difficulty tailoring his response to the situation, which includes differentiating the information needs of listeners. He is just as likely to go on and on with a classmate as he is with the teacher or professor.

Saying too Little
If the AS person is not interested in a topic, his answer is likely to be short. To illustrate, correct but short answers to essay questions are a constant problem for AS school children. The student may have mastered the subject matter, but doesn't "see any need" to expostulate on it. AS adults are likely to treat conversations in which they have no personal interest in the same way. They may abruptly walk away or turn their back, leaving others confused or insulted.

Humor
AS individuals do have a sense of humor, but it can be creative and idiosyncratic. If an AS person is very verbal, his humor often involves making complex puns. This reflects his advanced, dictionary-like vocabulary. Some AS individuals haul out entire memorized scripts from comedy shows and put on the whole show, whether or not their audience is interested or amused. They also enjoy humor if a story includes a familiar topic or punch line.

AS individuals do not like practical jokes. Even if the joke is harmless, their response to them is way out of scale. They are likely to harbor resentment for having been "victimized" for a long time.

If a joke made by others involves something unfamiliar, an AS individual may be totally lost. (The response is a blank stare reminiscent of Data in Star Trek.) It may take the person a while to process everything. Their reaction and laughter may be delayed or subdued. In other instances, once having been given explicit information and clarifying the meaning, they may join in the laughter.

Proving One's Point and Getting Things Right
AS individuals have problems identifying their emotions and the emotions of others, problems that can lead to outbursts of frustration, anger and rage. To convince others of their point of view, some individuals become argumentative, righteous and persistent beyond reason. Passive AS individuals might go silent or withdraw from the same stressful conditions. AS individuals are unable to learn social manners simply by watching others unaided. Behaviors and ways of doing things that come automatically to others must be taught step by step. Once the individual learns the basic steps, the other component to manners mastery is role-playing the behavior. Only through role-play may an AS individual learn to distinguish proper responses from socially inappropriate ones. For example, patient instruction can teach a 12-year-old answering the family phone with "Hello" rather than a gruff "Who's talking?"

 

Impaired Make-Believe Play

Parallel Play
Under unstructured conditions, AS children are often observed engaged in their own, separate play activity despite the presence of other children. This is because AS children do not understand the imaginary play of other youngsters their same age. They are unable to understand the projected emotions of others or imagine that others have emotions different than their own. For many AS children, their version of play hinges on the safety of scripts and dialogue memorized from movies, videos or favorite stories told to them.

Repetitive and/or Age-inappropriate Play Activities
If they favor play figures or dolls, AS children may act out these scripts in creative ways. Creativity with roles and ability to fashion complete and novel fantasy parts is more common in girls' play than in the play of boys. Boys are more apt to engage in endless repetition of the same memorized scripts or act out roles in more violent ways than girls. AS girls may desperately hue to the social scripts they see being acted out by their peers, or reject the expected social roles of girls by engaging in tomboy behavior or other kinds of activities not favored by their age-mates.

As they get older, many boys remain infatuated with role-playing fantasy games, a special interest that often follows them into young adulthood. Video games and role-play games involving cards and complicated scripts engage the attention of many young AS adults to the extent that moving into more adult game and leisure activities becomes a problem for them. Young AS adults with such interests often seek one another out, continuing a pattern of "group parallel play" difficult for non-autistic young adults to relate to. Friendships can develop from mutual involvement in such young adult "play groups", but just as likely, connections remain instrumental and focused on mutual enjoyment of a limited and predictable range of activities. AS individuals are at a loss when their companions lose interest in these activities and drift away. They do not know how to expand a friendship or allow it to move through stages where other's different interests provide the basis the basis for continued involvement.

Some young AS adults continue their play activities with child-age play objects, such as small stuffed toys or action figures. While such objects offer them comfort, the later on in life they continue to choose such play objects, the more difficult it is for others to make contact with them and pull them out of their I-centered world into the social life of non-autistic adults.

For AS boys, finding acceptance with their own age-mates is a great challenge. As mentioned above, they will seek out adults, engaging them intellectually as a result of their specialized knowledge, and less often just for unstructured social interaction. In response to their not understanding the play of their peers, they may prefer the company of younger children. This way, they can demonstrate an advanced mastery and take charge of the play experience of their playmates. The danger to this type of age mismatch for boys comes when they reach puberty and are seen playing with much younger children. Although the boys' experience is commonly devoid of sexual overtones, adults in charge act unfavorably to such arrangements. When their parents or caregivers remove these younger playmates, older AS children may not understand the reason. This is because they find it difficult to understand the intentions of others, or that others have different concerns than they do.

Because of differences in socialization, AS girls are less prone to seek out differently aged playmates. Age and developmental hierarchies are more rigidly enforced between girls than boys. (Attwood, 1999; Thompson, O'Neil and Cohen, 2001). AS girls are likely to suffer more from depression as they are rejected by their age-mates, and are far more likely to internalize their anger than boys, whose aggressive responses to rejection at almost any stage of childhood is more accepted. Out of desperation to be accepted by both sexes, later adolescent and young adult AS women stand a higher risk than AS males of becoming promiscuous and engaging in risky social behavior.

Memory
AS individuals are known for their remarkable memories. There is a social disadvantage to having a capacious but unselective memory. In many settings, they use their recall of facts to "win" arguments. Details long forgotten by others have a disturbing way of resurfacing especially when an AS individual acts to "remind" others of facts which, though correct, are irrelevant or don't fit a current context. Arguments often arise when the AS person demands that a present situation match their recall of a similar event or experience from the past.

AS children and adults are great historians, especially about events that they participated in. (if you want to review what happened last Tuesday at noon, and who said what, ask your AS child or AS partner.) Their desire for sameness and adverse reactions to any current variation on an historical theme are responsible for their abrupt reactions to change.

There is another unpleasant social consequence to having total recall. AS individuals may uncritically divulge things to others that were told to them in confidence. They feel compelled to share all, thus breaking confidences and hurting feelings. They are unaware of the intention of the person who confided the information. They may disclose secrets out of anxiety to say something during a lull in conversation. Individuals who have been betrayed by this conduct may avoid additional contact with the AS individual. They are so often taken aback by the disclosure that they can't convert the situation into a “teachable moment” for the AS individual.

Peculiar Patterns of Intellectual Abilities

As seen above, AS individuals have strong but relatively constricted interests. They may develop them as children and persevere in their pursuit of knowledge in the same topic throughout their lives. Other individuals develop strong but successive interests, moving from one intense perseveration to the next. Many AS children and adults, regardless of whether they are introverts or extroverts, become known by others as "little professors". Many AS adults actually do become teachers or professors due to their considerable knowledge on one subject. Universities and research institutes are perfect homes for persons with exquisite and arcane knowledge. Even if the AS person does not master many of the social conventions of professional, academic life, disciplines such as linguistics, mathematics, esoteric areas of science, accounting, and information technology all tend to attract individuals of both sexes who were earlier known as geeks, but now have perfectly acceptable titles and tenure.

Repetitive Phenomena of Rituals
Unanticipated change is the major stressor for AS individuals, but even when change is scheduled and known well in advance, AS individuals still experience inordinate amounts of anxiety about it. For autistic individuals, repetitive rituals and behaviors are means to gain a personal sense of self-control in constantly changing, unpredictable environments.

Individuals later diagnosed with Asperger Syndrome are sometimes earlier diagnosed with Tourette's Syndrome (TS) and Obsessive Compulsive Disorder (OCD). Some TS diagnoses are written very tentatively, as though the diagnostician made the best guess but still wasn't sure. Autistic childhood vocalizations (echolalia) are often accompanied by repetitive motions (echopraxia). Both behaviors occur as the autistic child experiences stress (from any source, internal or external). Some children diagnosed with TS make regular return trips to specialists who continue to confirm the diagnosis far longer than were the child to be seen by a new diagnostician at the same time. What many TS specialists "confirm" are successive, repetitive autistic ritualistic behaviors. As those behaviors lessen in intensity and frequency as the child matures, the child is pronounced "cured" by the specialist but rarely does the patient lose the diagnostic label. General medicine providers seeing the adult continue to refer to the childhood diagnosis and continue prescribing medication for their patient's "non-condition" without conducting any evaluation of the effectiveness or of their prescriptions. By history, they are prompted to look for TS, which they don't find. If they don't look for autism, they don't find ASD either.

OCD may be present in childhood and adulthood, and is a closer behavioral description of the social distress many autistic individuals experience from their ritualistic behaviors. While both childhood diagnoses may be correct, the function that ritual and repetitive behavior and vocalizations serve for the autistic individual is quite different than either purpose or function in TS and OCD.

Comforting Issues

As higher functioning autistic individuals mature, their expressive vocabularies can expand as they move through a succession of echolalic and echopraxic activities more closely approximating "appropriate" behaviors much less disturbing and distracting to others. Under conditions of stress, their need to engage in these activates -- which they find calming and "centering" -- does not disappear. As they move into adulthood and gain greater understanding of the concept of social appropriateness, they find places and times to let themselves go without upsetting others. However, for AS adults experiencing extreme stress, their behavioral response may regress to forms of reaction that typified much cruder childhood behavior.

Most adults with AS find working with people to be a very stressful experience, mainly because people are not predictable. Many AS individuals engage in repetitive activities or prefer mindless work tasks. Fondness for doing things in a rote, mechanical manner has a calming effect allowing the AS employee the time and an officially defined job task guaranteeing them a means of dealing with confusion they experience in otherwise challenging environments. These repetitive tasks are also readily given away to them by other workers. AS individuals can master such activities and perform them with accuracy, speed and ease. Following routines by the book, they may perform far better than their non-autistic workmates.

The intensity of the AS individual's adverse response to change is directly related to his desire for routine, sameness and to be in control. In all cases where AS individuals become upset with change, it is because they haven't developed an efficient mechanism to exert socially appropriate control over themselves or the situation.

Many AS individuals develop patterns and routines that must be followed. Predictable bedtime rituals are common with children, but just as common, though less noticed in adults. Dependence upon a set, ritualistic routine is commonly found with eating habits, self-care, and approaches to common personal, household or work tasks. This routine is not negotiable—it must be followed—and if interrupted, it has often been noted that an AS individual must start the full routine over, from the very beginning. They are not able to restart in the middle of the routine, and they are not able to accomplish the task without following that routine. If the AS individual is in an adult relationship or in a family setting, their rituals often have the effect of "terrorizing" other members of the family into submission to their routine. (McCabe, 2003; Stanford 2003)

Socially challenged AS adults may act impulsively, changing jobs and locations with the hope that the next change will "fix things". The fix doesn't happen. Given their dependence upon routine but their poor self-understanding of how badly they respond to change, in their new settings they re-create their favored routines in desperate efforts to surround themselves with conditions they can predict and control. Through successive moves, they rely on persons important to them to remain unperturbed by uprootings and upheaval caused by moving. They are often oblivious to the pain and discomfort their impulsive moves have on family members whose other relationships are constantly under threat with the prospect of yet another move in the future.

Other AS individuals, desperate to stave off the effects of change over which they have no control, hang on to a situation or a relationship for dear life, long after the life has been squeezed out of the arrangement due to their reliance on their helper-type partner coming to their rescue.

Providers working with AS adolescents or adults must be sensitive to the social context in which the AS individual operates. They must understand that if the individual is a "loner", unemployed or frequently unemployed, disconnected from effective support services or not in a relationship, their client's awareness of the world is vastly different than AS individuals who have made significant social connections. Loners' social-problem-solving skills are likely to be rudimentary and very inefficient. Because of their disconnectedness, results of their poor decision-making are confined to a small circle.

If the AS adult has made significant progress in the social world of adults, the perspective of any helping professional must widen to include everyone touched by the individual. Adult problems are far more complex than the problems encountered by children. The consequences of making a bad decision can be far-reaching, affecting the lives of many persons in the AS adult's life. When AS individuals marry and have children, consequences of indecisiveness and/or impulsiveness in inefficient adult decision-making and poor parenting affects the whole family. As a result of repeated experiences of poor problem-solving by the AS parent in an intact marriage, the higher functioning partner may "close" the family to the outside community, averting future embarrassment and shame caused by the past conduct of the on-spectrum partner. When families become closed, either as a result of an autistic adult or an autistic child's behavior, the closed character of the family presents special challenges to community service providers.

An Interesting Exception
All individuals diagnosed with AS demonstrate unusual responses to change. Without being prepared for anticipate change, AS individuals have difficulty responding to new problems. However, if their "data bank" is large enough, they may be the cool one in situations where everyone else is in a panic. This is because they've learned the drill to handle such emergencies. The one thing they know how to do is take control. This fact may account for the successful law enforcement, corrections, military, and first-responder careers of a few people with Asperger Syndrome. Others defer to such persons. Rules governing their roles call for them to be in charge.

http://www.pediatricneurology.com/autism.htm#Asperger’s Syndrome)

 

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Comment by GUEST on 2008-10-01 19:05:49
I don't know where to start. I pushed my wife to participate with the family rather than spend all her time reading romance books and playing on line game called world of warcraft. After 14 years of marriage she said i did not make her happy and she divorced me and started a relationship (in character) with her on line boyfriend. It has been two years. She has seen him physically twice and they played wow together. She doesn't call our children. We have been divorced for 1.5 years. The therapist first mentioned as. My ex's one brother was severely autistic, her other brother is homeless and plays dungeons and dragons rather than work. Her father who is 62 bikes 3,000 miles a year and junk picks bikes and puts them all over his yard. When I first met her, her family would communicate by putting notes by the table where they sat. He father didn't say he loved her until I brought it up when she was 33 years old. He mother has schizophrenia severe and is in a group home. I am an extreme extrovert and very empathetic. I knew something was up but couldn't figure it out. I still miss her. My kids are super happy she is gone. They do not want me to even attempt to reconcile. I could go on about our 14 year marriage. During our drive to Florida on our honeymoon she read romance books and was annoyed when I'd point out interesting things by the road. It all makes sense now. But now we have no family. I thought she was just overly shy. She refuses to get diagnosed officially and now wants to become a nurse even though the college told her it would not be a good fit. She was fire from Target because she refused to talk to customers. My heart aches and I think about how she is doing. I fear for her. But this week she moved back in with her parents (dad and step mom). I pray she has a good life. I blame myself for the divorce... had I known maybe I could have adapted to her? woulda coulda shoulda... I want to turn around my bad experience into a good one and help AS people. 
 
AsPlanet reply: 
Thank you so much for that, it saddens me that so many of us become alienated from society in general... as we often feel the need to alienate ourselves as a safeguard, please do not blame yourself... you were not to know. But maybe now you can start to help, be a support to her and maybe help her children be apart of her life again. That may not be easy, as we hate change and often if forced into situations will withdraw more into our own.  
 
But you also have to remember its her decision to be diagnosed, not yours, and if you approach her she may be quite defensive at first, also I do not of course know your whole situation. But personally if someone had told me, I may of dismissed them, but I know I would of wanted to know more in my own time and way, and would of been very grateful eventually. You could mention, but would not force the issue, that has to be her choice and decision.  
 
But growing up myself with a mother who could never be there for me, I know how hard and sad it can be to be disconnect from your own children. Somehow, I have survived and only just realized many of my problems in life, my own differences were not because of my own mother, everyone else, but because of my own differences and being at odds with a world, that often does not understand, get or allow for differently minded people such as myself.  
 
I only discovered aspergers and me just over 1 year ago, that's not easy in itself.. it feels a little like my whole life has been wrong up until now, not only has it caused me great pain not knowing, I have unintentionally hurt others. I  
know only too well what a hostile world it can seem to some of us that through no thought of our own, can be judge and misunderstood so wrongly. 
 
But having people such as your self, who have lived with a person, who is unable to connect with, unable to understand, on your terms and realize this is a real problem, as you know yourself you can not change the person, within families we all have to learn to change adapt and make allowances for differences, it can work, its beginning to work better than ever with mine... but takes time..  
 
so thank you for taking the time to tell us your prospective, it does help to be reminded that we impact on others... as for me at first I was angry with the whole world, but now I have to face up to how I have hurt others, as well as trying to fit some where.

Comment by GUEST on 2009-01-09 05:56:40
I am a 17 year old high school student who was diagnosed with Aspergers syndrome 2 years ago. Despite being a normal adolescent and having normal friends through middle school, I later began to develop anxiety problems due to a series of traumatic events that occurred while I was in junior high. I had always been a little shy in the past, but my social anxiety seemed to elevate drastically and I began to have difficulty with verbal/non-verbal expression and maintaining eye contact with people I spoke to. Social gestures I used to be able to do unconsciously I now have trouble with. I've become introverted and distant with everyone around me. I no longer have an interest in pursuing social relationships for fear of rejection. As I walk past people, my body movements become stiff and awkward due to the anxiety of being perceived as strange or disabled. I now have an immense fear of public humiliation and tend to do all that I can to avoid all social contact. At first, I embraced the diagnosis because it seemed to be the only explanation to my problems, but recently I've begun to examine my symptoms and they match the criteria for Selective Mutism exactly. I don't exhibit any of the repetitive behaviors that other individuals with ASD have. I am enrolled in a specialized school now but I feel maladjusted and desocialized. While normal people my age are maturing and pursuing happy lives, I cease to progress. I've become extremely depressed and have had thoughts of suicide. Have I been misdiagnosed? What should I do? 
 
REPLY: 
Your really need to speak to a professional, I would first speak with your own doctor tell them how you are feeling and what you have wrote here.... its not easy to get diagnosed let alone be misdiagnosed but it can happen. 
 
It's not easy dealing with being diagnosed with Aspergers as a young adult, as 
peers may no longer be willing to tolerate someone who seems different. A misunderstood difference at this age often leads to Moodiness, depression and anxiety, impacted by hormonal inbalances, and feeling like the outsider, the age when you disparately want to fit in. 
 
Not having anyone to share your deepest, darkest secrets with, or feeling not able to because of the lack of understand or reaction if mention on the autism spectrum, never easy because of lack of good knowledge and understanding of being different and the stigma often so wrongly attached... once diagnosed it takes time to accept, really understand and allow and with that comes confidence of self... 
 
To me selective mutism comes under the bigger autism umbralla, a neurological difference. Its not about the label its about understanding self and accepting our differences as part of who we are, if your not happy with your diagnosis see someone, as obviously in your mind there is something wrong, or something that has not been explained to you in full and/or if depressed sounds like you need more support, but being on the autism spectrum is quite complex and no two people are the same, there is no one stereo type image as many think. 
 
The Asperger AQ Test http://aq.server8.org/ is a good general test and indicator, but my advise is see a professional, as better to have confirmed and learn to deal with either way, things always seems a lot worse unless fully explained, I can not do this as do not know your case history or much about you, I am just telling my story in the hope it reaches out and helps others have a better understanding, but whatever the outcome your not on your own, my older son was diagnosed less than a year ago, now 15 he is fine and most of the time no one would know, he just is himself and his quirky differences are what makes him the unique individual he is. 
 
If your feeling down its hard to have confidence in self, who ever you are and what ever difference you may or may not have, remember no 2 people are the same on this planet would be boring if we all were and each and everyone of us is born with unique traits some more different or as I like to say more interesting than others, take care and get help/support not easy dealing with in thoughts... 
 
__________________________________________________ 
Comment by GUEST on 2009-01-07 15:01:42 
How often is Selective Mutism misdiagnosed as an ASD?  
 
REPLY:  
Interesting question, may be better to ask on forum as get more response... not some think I have really thought about, just sharing my asperger journey, I am not a professional myself, but feel Autism / Selective Mutism misdiagnosed - I guess it happens... errors are often made in the professional world like every where else. No one has all the answers to autism or all the links connections yet and to me autism is the heart, the core of who we are and many of us have varied additional co-morbid, associated conditions. Selective mutism is an anxiety disorder and nearly every person I know on the autism spectrum suffers from anxiety at some stage! Many of the traits of selective mutism are also so similar to autism that I can not help but wonder just another name under the bigger autism umbrella....  
Professions have a tendency to label every part of difference they do not understand and/or to be able to treat.... over the years feel far more labels acquired than really needed.Labels change with progress...  
 
"The way I see it: Apart from being on the autism spectrum I have many co morbid / associated conditions… in fact a whole list, not sure anyone has it right, including myself. Often our labels can get over complicated... and near impossible to know which bit is which, with many overlaps, but any label does not change who we are. I have my own simplified version - The center as I see it, is us - the Autism heart, differently minded part... which to an extent feel many NTs just do not quite get or understand. So often the most important thing the centre, gets neglected, so it’s no wonder we are often a little off balance.  
Surrounding the center are a web with many chaotic paths, often disjointed and ineffective, as these neuro associated conditions, co morbid mental disorders (or misunderstood difference), environmental factors are all blamed and continue to circle around the most important part of us. I feel its time other started with the centre - the Autism Heart, forget the labels. Because if our hearts were balanced and allowed, as I see it. A lot of these existing links in the web, may start to fade... I feel many of the labels are often caused by others misinterpretation, dealing with small aspects of the whole person, often neglecting or not understanding our centers from when we are born." [Alyson Bradley - August 2008]"  
 
I have quoted this para as describes really well selectively mute and autism, plus see link interesting read with many autism comparable's:  
"Although children on the autism spectrum may also be selectively mute, they display other behaviors--hand flapping, repetitive behaviors, social isolation even among family members (not always answering to name, for example), sensory integration difficulties, poor eye contact--that set them apart from a child with selective mutism. If a child is simply not speaking in social situations, this is likely not an autism spectrum disorder, but may be selective mutism. Children with selective mutism are not necessarily autistic, but children with autism, which has a large anxiety component, frequently display symptoms of selective mutism. It is critical to have a child with these symptoms evaluated by a developmental pediatrician."  
http://en.wikipedia.org/wiki/Selective_mutism

Comment by GUEST on 2009-01-15 16:09:22
What age do people with Aspergers/HFA start driving (if they ever drive)?  
 
REPLY: 
Interesting question, while many do drive and very well it depends on many things. Myself even though passed my first test, as tend to be able to do anything I put my mind to, but as with most things learned in my own way, do things in my own way and so fitting in on the road never quite worked for various reasons, lack of support at times, funds to have enough lessons,lack of confidence, never needed to as grew up in London, too much inter action with others, too many detractions for me..and when I was learning no one understood my differences, including ,me at the time... but with the right support I feel I would be driving now and wished still at times I followed through and could, in theory I have a license, but would need a lot more lessons before driving again. It may take a little longer to get there, but truly worth it, age or our differences should not hold us back, its often lack of support or understanding from others that does...  
 
I also have dyspraxia and find "To be able to steer a car, concentrate, judge distance, use both hands and feet together and remember how to carry out a sequence of tasks all at the same time is very daunting...." 
See Dyspraxia Foundation - Driving: http://www.dyspraxiafoundation.org.uk/services/ad_driving.php 
 
But I guess I have quite a few associated conditions dyslexia just another one from my list... so it really also depends on your associated, co morbid conditions as each and everyone of us are individuals, but if I could now if had a very patent instructor and the money... 
 
Luckly there is someone who now specializes, realizing there is a need in chch, south island where I am and world wide becoming more recognized... if the UK the dyspraxia foundation will be able to advise...  
 
It is advised that all asd people should also have special eye sight tests or at least advise your the optometrist your on the spectrum and for learning to drive there are some specialist. I had many sight problems and my sight was not good enough to drive anyway for part of my life, but even without sight problems many of us on the autism spectrum have peripheral vision problems, I tend to sense more than see in these areas and that can be a real problem for me driving... 
 
Also LEARNING IN A AUTOMATIC CAR helps a lot, and is often advised, less distractions, the gears is what I found hard, to much for me to concentrate on.....  
 
But with the right support, there is no reason why you should not drive if you really want too, as many do and I feel the younger the better to start, quicker responses etc..... good luck 
 
More on this on AsPlanet forum - DRIVING and DYSPRAXIA and Dyslexia!:http://asplanet.info/forum/index.php?topic=5.0

Comment by GUEST on 2008-02-15 06:09:46
Thank you very much for posting this great resource. 
Rosie

Comment by GUEST on 2008-02-21 21:51:05
Thanks for this detailed and concise source of information, I've found it to be very helpful in gaining a better understanding of this subject. 
Elaine

Comment by GUEST on 2008-03-01 18:48:10
Thank you so much for helping me and thousands of others to understand their condition. 
Gwenda

Comment by GUEST on 2008-03-17 22:09:12
What a wonderful source of information! Thankyou 
Heather 
 
Thank you. So helpful. Evangeline

Comment by Guest on 2008-03-20 04:32:17
I'm currently in the process of getting a diagnosis, I am seeing a psychologist who specializes in aspergers, and it really helped me understand some of the symptoms. It explained a lot of my childhood. I found the DSM-IV criteria did fit me, but found that the long explanation of the 5 characteristics of autism fit me like a glove.  
All that to say, thank you for the website, it was very helpful.

Comment by GUEST on 2008-06-01 04:33:49
I think my husband has AS. I don't know how to handle it. All this information is very useful. Thank you. 
 
Reply: 
If your husband does have it, it can be hard living with someone who does not understand there differences, but the decision as an adult has to be his... unfortunatelly quite often people do not want to know, as see it as some sort of fault within themselves, which of course is wrong - its just a difference. 
 
I would suggest reading as much as you can yourself and truly understanding this will help you understand any differences, then if you feel really sure speak to your husband about it, if you can.  
 
Maybe start with the AQ test top of this section, he may not react at first, may not want to know, but if he is on the autism spectrum may want to do in his own time and deal with himself, can be a bit of a shock at first, so try not to force the issue, as no one can change over night whatever the reason for there differences. There is no easy answer or fix, but knowledge can make a huge difference.

Comment by GUEST on 2008-05-20 18:46:58
Finally, a detailed description of AS that fits me like a glove. I have no 'official' diagnosis yet, and have struggled to understand the language of the DSM etc, yet if I had any doubts at all that I have AS, you have just removed them. Thank you. 
One final thought - that both the aggressive and the passive, self-harming types of AS are 'natural' responses to a world that doesn't accept or understand them.  
 
Reply: 
I agree with you 100% that"both the aggressive and the passive, self-harming types of AS are 'natural' responses to a world" unfortunatelly I feel many of us have been damaged by society, wronly diagnosed and misunderstood for years... 
Alyson

Comment by GUEST on 2009-02-23 02:25:53
You are so right in that Alyson, I know I've had copious negative reactions simply to being me, and all the research and reading I've done suggests it's all too common. Why are people so determined to make us like them?!? Aren't we allowed to be different?

Comment by Guest on 2009-02-25 06:37:00
Your site is great, it has certainly help put things in perspective for me.  
 
I found the bit on driving really interesting, I also rarely drive, but know I can. Just have always found extremely stressful but never understood why and only really drove auto, so what you say makes a lot of sense. 
 
Thank you

Comment by GUEST on 2009-02-13 17:23:43
My father told me I was born with autism, a disease for which the prognosis is never very good, but my mother told me that when I was a few months old, my father flung me across the room like a rag doll and I landed on my head and that she had to cover for him for fear he'd lose his job. I've also read that trauma like that in the first year of life usually screws a person up for life. 
 
REPLY: 
First "my father flung me across the room like a rag doll" that is horrendous, I really dislike bullies at times, but often sad individuals themselves who need help. Many of us on the autism spectrum have suffered, lack confidence and often because we are bullied by ignorant people who often feel they are inadequate because they can not deal with us.  
 
Every aspect of life affects us in one way or another, we are who we are for many reasons, autism is not a disease - neurologically we are wired differently, differently able, but those of us on the autism spectrum are as diverse and different as those that are not, with often many associated, co-morbid conditions, varied circumstances..... but the one thing I feel we all have is an autism core, I call it our Autism HEART often our biggest problem in life is others not understanding us.  
 
Parents who have children on the autism spectrum often try and find reason, label blame somewhere, fix (I hate that word) their child, instead of trying to understand, accept and allow these children to be the differently able individuals they were born as. Sometimes I feel parents worry so much about what everyone else thinks, they forget about whats right in front of them, they forget the fun and joy every child can bring to this world...

Comment by GUEST on 2009-02-13 06:15:22
What would your life be like now if you hadn't been diagnosed with HFA/Aspergers? 
 
REPLY: 
First I have been diagnosed with Aspergers Not HFA, because of my many associated and neurological differences I have as many weaknesses as strengths and see my self as differently able and to me its not about being diagnosed or the label so much as being able to understand self and coming to understand my symptoms,differences.  
 
Good question, first I guess I would have been still looking for answers... there has always been some think missing, wrong somehow. There are so many things that would be hard to put as just a reply as a comment and if you read some of the articles like "making sense" in my profile your start to get some idea. Not an easy answer and no quick easy reply, our lives can all be what ifs, I am glad this part of my life is not... in fact writing a book about my journey finding self etc.. at present, but its more complex than just being diagnosed or not, my life journey will always continue and its hard to say what may of been. 
 
I guess I would not be thinking about asd now, the injustice of growing up and being made to act and be like what never quite worked or fitted.... before I had as I see it no real,true identity, real sense of self... I made excuses for things that never made sense, I lack reason some how, not being like others with no answers often made me feel inadequate.. so since discovering my biggest discovery Aspergers I have been on a roller coaster of a journey discovering other associated conditions, neurological differences and its taken a while, but I now feel confidence to start to be the person that has been lost for so long, many of my unanswered questions in regards to how and why I do things have now been answered, who I am and that dark confused secret no more, not even sure how to explain that, its like thinking your depressed but knowing your not, like when you sense some think is wrong but have no idea what it is, but its always their! 
 
So I guess if I hadn't discovered Aspergers I would be continuing my life on an almost self distract button, no real sense of being or purpose. One of the most amazing things on my journey has been for the first time in my life I have found so many others like myself, who understand and I can relate to and no longer need to feel sub human.  
 
To not know to me would be like being imprisoned for the rest of my life, I feel free... so if did not discover asd it would of been like with every step forward, the invisible cage would continue to hold me back... I guess its the difference from just existing or really existing. Young children may know no difference when very young but hurting them is wrong, has long term effects, the same I feel is to not diagnosing asd adults or anyone on the autism spectrum, the longer asd individuals continue to be in the dark about real self the more damage and harm long term I feel is inevitable.  
 
I am not an expert and do not pretend to be, I can only tell my story and that is one of many... life is a choice for all of us, asd was one of my better choices, discoveries in life. All I know I do not cry for no reason any more, there is no longer a deep sadden that just didn't make sense, I no longer need to pretend I just am... 
 
But as for all of us what would any of our lives be like if we did not search, did not seek to find answers...  
 
Truly being diagnosed with AS it was a HUGE relief, everything starting making made sense! And not only did it make sense, I was able to start dealing with things I never understood, or realized about myself before...

Comment by GUEST on 2009-02-09 14:18:09
Can Autism be caused by distant parenting? 
 
REPLY:NO 
Autism has no class or race barriers, the individuals are as varied as the parents and for those of us on the autism spectrum each one of us is as different as the next, just like those of you not on the autism spectrum. 
 
To me autism is a way of being, its not caused I was just born neurologically differently minded /able. Autism isn't caused it just is, as a parent often we should not see misunderstood difference as thought. All children who ever they are need to be allowed, accepted and understood at least by their parents, with autism there is lack of real awareness, and it can be hard for parents to know which way to turn. I am a mother of an aspie child, have Aspergers myself and its taken me almost half a life time to find true self, of course we change, adapt as we grow, what ever our circumstances. 
 
I may never of known about ASD until in my forties but I never lost my autism core...The way I see it apart from being on the autism spectrum I have many co morbid / associated conditions... in fact a whole list, not sure anyone has it right, including me. Often our labels can get over complicated and near impossible to know which bit is which, with many overlaps, but any label does not change who we are. I have my own simplified version - The center as I see it, is us - THE AUTISM HEART which is the differently minded part, which to an extent feels to me many NTs (the average person) just does not quite get or understand. So I feel often the most important part of us the center, gets neglected, so it's no wonder we are often a little off balance. 

Surrounding the center are a web with many chaotic paths, often disjointed and ineffective, as these neurological associated conditions, co morbid mental disorders (or misunderstood difference), environmental factors are all blamed and continue to circle around the most important part of us. I feel its time others started with our core, the center - autism heart, forget the labels. Because if our hearts were balanced fulfilled and allowed growing up, as I see it. I feel a lot of the existing links in the web, may start to fade. I feel many of our labels are often caused by others misinterpretation, dealing with small aspects of the whole person, often neglecting or not understanding our centers from when we are born. 
 
Those of us on the autism spectrum have some wonderful unique often under resourced talents, our quirky differences often keeping us on the edge of society. But some of the most brilliant minds have and continue to be on the autism spectrum, I feel its about time everyone embraced these unique talents and give us at least a chance, I will always have my autism heart how ever much others try and change or make me fit, a square will never fit a circle, so I cannot help but wonder why so many try instead on seeing what's right in front of them. If you really want to understand get down on your child's level and see thought their eyes, listen to those of us that have lived with being on the autism spectrum and continue too.... 
 
I believe autism is genetic, Rett Syndrome is and thats 100% genetic and is also a type of autism! 
There is no real fact for autism just like the universe... 

Comment by GUEST on 2009-01-31 05:44:40
Is there a link between schizophrenia and autism? 
 
REPLY: 
A good question who knows, I am not an expert in this field, so I can only give you my thoughts and experience as a person with asd. In the past people with asd were diagnosed with other things such as schizophrenia. i.e.Autistic psychopathy [Hans Asperger's term for Asperger's syndrome] 
Schizoid disorder of childhood [another term for Asperger's syndrome]! 
 
There are similarities and I know traits for both are in my extended family and other families I know. There are many articles on this and one of the recent ones is: Disorders like autism and schizophrenia - link!  
http://www.nytimes.com/2008/11/11/health/research/11brain.html?_r=1&em&oref=slogin  
 
I have only read up on, not researched fully myself. But I do know people with Aspergers Syndrome share many co-morbid conditions, core anxieties but present a wide spectrum of strikingly different character traits and coping devices. There exists considerable overlap with other conditions such as Attention Deficit (Hyperactivity) Disorder, Borderline Personality, Schizoid Personality Disorder and psychopathy. 
 
It has been said recently that "Schizophrenia and autism probably share a common origin, hypothesises Dutch researcher Annemie Ploeger following an extensive literature study. The developmental psychologist demonstrated that both disorders have similar physical abnormalities which are formed during the first month of pregnancy." 
 
Is there a link I tend to think there is, well a genetic component, but then like autism there are no real facts yet!

Comment by GUEST on 2008-10-28 14:13:59
I found Alyson's story through a research project. This has led me to find this valuable resource. So in depth, so honest and I really want to thank Alyson for sharing her thoughts and helping me to understand a little better about stuff going on in people's lives around me. 
Deborah Crewe

Comment by Guest on 2009-03-26 08:39:27
Your site is amazing not only up to date, but great supporting information, it has been more helpful than any book or article I have read so far, your deserve to be recognized for your amazing efforts to helping others understand ASD...

Comment by GUEST on 2009-07-01 18:57:38
My Son is Autistic he has had Sensory Integration; he Talks and has other abilities but can not write or type. How can help him? 
 
MY REPLY:First it depends on so many variables, First is there a reason he can not write etc.... what age!!! you should speak with his school if at school, and depends on totally where you are, what country your in to what support you may get for his associated learning difficulties, via special needs or relevant group, really depends on problem, more detail needed... 
 
Occupational Therapists of course can help with hand writing and if simply finds hard make fun, big bold and encourage, encourage, encourage...practice the key... 
 
As for sensory a huge one for individuals on the autism spectrum, something many of us have had to learn to deal with daily, basically its having to live in a society where we sense and feel differently from none autistic individuals and at times we have to deal with sensory overload, which can lean to anxiety exposure... for more on this see: Emotional Chaos, sensory issues overloaded, shutdown... http://asplanet.info/index.php?option=com_content&task=view&id=66&Itemid=110  
 
For more in dept discussion please join AsPlanet forum, members only but free and lots of advice already on associated conditions, but not only will I be able to give you more in dept advice, you could give us a lot more detail without anyone being able to view and others there to also advise... this section is really just for comments... but happy to answer the odd question here. 
 
Regards Alyson

Comment by GUEST on 2009-07-10 17:48:50
For some time now I've wondered if I may have AS. I worked as a psychiatric nurse for 10 years. During that time I met a lot of Aspies with whom I could identify strongly. I did some further reading and research (yep almost obsessively so), and the more I read, the more symptoms and behaviors seemed to fit.  
 
Just now I read the Aspie Adult Checklist at the top of this page, and it brought tears to my eyes. 20 out of the 30 things mentioned there match. 
 
I was diagnosed with clinical depression many years ago, and experience much anxiety and OCD behaviours. Now I am wondering if all three are actually manifestations of AS. I have my very first ever appointment with a psychiatrist next week, for a medication review to manage my current symptoms, but I think I might hit him up with this query about AS. I just hope he won't laugh me out of the office when I turn up there with my scraps of paper where I've noted my symptoms down. Now, I am off to explore this site! 
 
MY COMMENT: 
Never easy self discovering, like many of us a shock at first, but often also a relief as our life unfolds and starts to make sense.... 
 
Discovering if your on the autism spectrum, if you have AS can take a while and I often feel people are there own best judges, but it can take a while... to be honest the biggest misconceptions of people being on the autism spectrum is that we are all the same, we are not... in fact can be very diverse and different. 
 
It's not a matter of a simply check list, I wasn't diagnosed with any think until in my late 40s, and I have many co morbid, associated conditions. Autism is the center, the differently minded part, as for diagnosis.. I feel its best before thinking about being diagnosed, write down as much information as you can will really help, back to when you were a child. As we get older we learn to change and adapt, does not mean we do not still have those differences, do what your doing now research and read as much as you can and then decide, if you feel you are I always say its best to know for sure before being diagnosed, as its not about the label, its about true identity. 
 
Some things you can do, list, criteria ands test: 
AS Symtoms (Full Official Criteria) and take the AQ Test: 
http://asplanet.info/index.php?option=com_content&task=view&id=29&Itemid=63 
 
Some threads on asplanet forum which may help you start your own:ADULT Characteristics ASD 
http://asplanet.info/forum/index.php?top... 
My list of Characteristics of Children to Adolescences AS symptoms, as also always good to jot down symptoms as a children, we may change and adapt, bt the traits stay... 
http://asplanet.info/forum/index.php?top... 
 
The forum is free, memebers only just so that more private, but va great place to find more information and offload all your searching questions.... good luck with your search and please feel free to email me anytime. Alyson questionsI

Comment by Guest on 2009-07-15 07:54:12
Keep it rolling in to all you mums. Remember the truth about Aspergers I am blocked from talking about it but thats ok. Remember ASD is an intellectual state of mind.Intellectual potential for all who have Autism, its only a social disability. At the age of 8 it Dawned on me that I could think about subjects in a different way to others, that's not just a basic reality. But thinking out side it, to me Autism is natural and is a typical progression for the well being of earth (Fact) 
 
Master of intelligence just read about me David rs Greer I live in Nelson New Zealand and am 33 and wonder why my comments had been removed for talking about the (MMR) from sights! 
 
I do have a question why are people trying to stop it ."Most autistics, in fact, do not want to be cured because they've already accepted autism as part of their personality, Identity and lifestyle," he wrote. "You may not understand why anyone would want to be diagnosed with a psychiatric condition but even homsexuality was listed in the DSM (Diagnostic and Statistical Manual of Mental Disorders) as being a disorder at one point in time." 
 
Funny that I did not think Aspergers was a psychiatric disorder or is it. 
I David rs Greer still ask that! 
 
Its other people who shy away from helping because they call it a intellectual disability.I have been turned down for mental help for bullying and how to deal with it in Nelson. Sad ? 
 
and yes I have Aspergers syndrome and wrote this my self..Hear is my word for to day please have a coffee intellectually therapeutic. 
 
 
MY REPLY 
Hi David, yes I am a mother and I do run the site and support forum along with the help of my son, but also share stories and views from a wide range of spectrum and others individuals, to celebrate, share and support, a sort of coming together... 
 
I am not sure why you have been blocked from many sites, but in this world if we do not communicate, conform to the majorities standards we often we not quite fit, for that your not alone. But guess as with all networks there has to be rules or would be Internet chaos, I have many riles on my support forum, but that is to protect my members from spam and wrongful use.  
 
I agree we have many strengths and with that often weaknesses also, while Aspergers is NOT a psychiatric condition, often many on the spectrum have co-morbid conditions and some have psychiatric conditions, but so do many people not on the autism spectrum. 
 
As for my views on MMR simply fact while it saves lives I agree with, yes there will always be the odd child that reacts and who knows the answers so quest a choice. More on my views as not really a yes or no answers. As for cure while I agree to a point with you, and happy with my differences I understand how ignorance or having a child who has brain damage wanting them cured, but the brain damage or often other reasons are not the autism as such! for more of my views on both see link in sub menu under AS Symptoms "Vaccines / cure!"  
 
If your post are being removed maybe the way you are wording things could be offensive to others. Or could simply be hard to read, I correct for you sometimes and know how hard to put muddle thoughts down myself as I am dyslexic and often have to check my own post a few times so that other will be able to make sense of. 
 
Sorry to hear you have been turned down for "I have been turned down for mental help for bullying in Nelson" not sure the reasons, but maybe if feel you are not getting the support you need speak with your doctor, they should be able to help, make suggestions. 
 
and I agree a coffee always good :) take care Alyson

Comment by GUEST on 2009-09-10 03:54:03
dear alyson: i am a young teenage girl with aspergers ,and I found that a lot of the things you said above resonate with me right now i feel as though i might cry 'cause everything is true.i also didn't know that there were so many famous people who had it,esp. movie geinus speilberg.sometimes i feel like a circus freak for having this condition. i am very worried about being accepted by others in my class.please help---------gaby 
 
My Reply: 
Hi Gaby the answer truly is being able to understanding self fully, accepting and allowing as its truly not about any label, there is no one way and it simple means with understanding we can allow, brillinat for confidence and self esteme, at first can be a bit of shock, growing up without being fully embraced or understiood. 
 
Myself I will never fit into any set of tick boxes as they are only generalizations, as each and everyone of us on or off the vast autism spectrum are so varied and different, we are all born as unique individuals and in fact autism comes under the bigger neurological differences and about 40% of all children have some kind of neurology difference, be it dyslexia, dyspraxia, adhd myself I have all of them as well as other differences and Aspergers. Most individuals on the spectrum fit in just fine, some of us a lot more complex with a lot more differences and its not so much the autistic part that many of us need the most help with, but often its the many co-morbids / associated conditions which anyone can have that affect us most... 
 
and to remember we are not disabled, no one is as such, but societies attitude often disabled us! thats why many like myself speak out, because so much more awareness and understanding needed in the world in general... come and join us sometime on AsPlanet Forum www.asplanet.info/forum/as you find your not alone, many understand and always someone who can answer all those questions, that often many none spectrum individuals find hard to. 
 
One of the best things about being diagnosed for me is that I found world wide a brilliant, intelligent extended family, who really understand and care :) as for crying I think we all did at first, it helps, but what has helped us all the most is having like minded individuals to understand and share with... take care Alyson

Comment by GUEST on 2010-02-21 06:00:37
A friend has suggested my 43 yr old partner of 10 years may have aspergers. After reading about it I think so too.  
 
I just wonder whether getting diagnosed would leave him or our relationship in a better place if there is no treatment. What would the benefits of knowing be? 
 
Also, how can I introduce the idea to him in an appropriate way so that he can check it out without feeling insulted by me. 
 
 
AsPlanet REPLY: 
Not easy because it really has to be his decision and choice, so maybe mention a quiz you have found in passing maybe the AQ test and do for fun, or simply email him it and leave it up to him, but I would not push the matter, he may not want to know, many do not.! 
 
Myself discovering Aspergers and all my neurological differences gave me my life back in away, so I see as a positive and think logical to strive for people to know themselves better,not just for diagnosis of "differences", but also personality, getting to understand and know our strengths and weakness fully and I do feel it’s important to validate us as individual’s. 
 
Another reason accurate diagnosis is generally a good thing, in case he doesn't have Autism, but something else, it affects what you can do to help yourself, although there is a big overlap between AS and several other conditions / intellectual learning differences etc...  
 
It is helpful for family and friends if they are interested about finding out things for themselves. Also generally as we get older we can get more set in our ways and feel it’s vital our differences are recognized so that others can fully understand us, how we impact on others another important factor, because without knowing, we do not know.  
 
Down side it costs, and not enough good professionals to diagnose. Also many doctors do not diagnose adults in some places, the consequence of this many searching start to question self, others do not accept and they stay in no man’s land, leaving them uncertain of self.  
For me being diagnosed even so late in life was the best thing I ever done, just made so many things make sense. But at the end of the day I feel it really has to be an individual choice to be diagnosed or not. 
 
But maybe for now keep reading and researching and be very sure first before saying, then maybe leave some information around, so can be found if he wishes to... If he decides to be diagnosed he will need to his doctor who will refer and/or advise, or can go direct to a clinic physiologist himself. But maybe you could talk to your doctor about and see what the doctor says, as what they may suggest and do different depending where you are in the world. 
 
I hope this helps a little, as a lot to take in at first, but do not rush into as he will need time, even if you mention in passing to think about, as it can be a life changing process. Personally what helped me the most and continues to is speaking with like minded individuals, some are diagnosed, some choose not to be, as mnay adults later in life decide, but understanding if he is can only help.. 


Last Updated ( Jul 09, 2010 at 07:37 AM )