Self-Diagnosed with Asperger Syndrome?

In the last few years, many adults with social communication issues have read about Asperger syndrome, taken a few online tests, and self-diagnosed themselves with the disorder.  In fact, I got a note from just such an adult today:

I'm 50 and suspected I had aspergers all my life cause I dont relate good with people [sic] and I have a lot of the symptoms but when i wanted to get tested for it, the psychiatrist talked to me for about 5 minutes and told me i didnt have it, and never tested me for it, but if i take an online test i pass it every time, any suggestions?

While taking tests online may not be a valid substitute for a full evaluation, the truth is that there are few professionals out there with significant experience in diagnosing adults with Asperger syndrome.  And while not every adult who believes he or she has Asperger syndrome is correct, it's likely that many are.  John Michael Carley, Director of GRASP.org (a support organization for adults with Asperger syndrome) takes it a step farther, saying "if you think you have Asperger syndrome, you probably do."

For adults with symptoms of (or similar to) Asperger syndrome, finding a diagnosis and a group of like-minded individuals can be enormously liberating.  By the same token, however, self-diagnosis can severely skew statistics - and can make the disorder appear to be less significant than it is.  What's perhaps worse, the term "Asperger syndrome" is starting to diverge from a diagnostic category, and to become more of a statement of personality and style.

Asperger syndrome, in fact, is not the "Geek Syndrome" (as described in a famous article in Wired Magazine).  All people with AS are NOT brilliant, technologically savvy, creative and intriguingly eccentric.   Some people with AS have a hard time with numbers, enjoy reading fiction, and engage comfortably with a wide range of people.  Some, on the other hand, are living with serious and debilitating symptoms that make it difficult to find or hold down a job, or even engage in ordinary daily life.

Is self-diagnosis a good idea for individuals who can't find a satisfactory professional evaluation?  How should self-diagnoses be announced to families, friends or employers?  Is self-diagnosis a helpful or problematic approach to understanding social/communication difficulties in adults?

Share your thoughts!

Did you self-diagnose with Asperger syndrome?  Share Your Story Here!

More About Asperger Syndrome in Adults

Join the Autism at About.com Conversation in the Forum or on Facebook!

Self-Diagnosed with Asperger Syndrome? originally appeared on About.com Autism on Sunday, December 26th, 2010 at 11:10:16.

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T’was a Chiropractic Christmas

by Author Unknown

T’was the day before Christmas,
but there was no cheer.
No jingle bells jingled, no sound of reindeer.
The word had gone out that Santa was sick.
There would be no visit from jolly St. Nick.

The people were sad; no gaiety sounded.
For Christmas had come,
but Santa was grounded.
He drove down the road,
and what should he see?
But a sign for a doctor, who was a D.C.

Now Santa was not one to like a new tactic,
But all else had failed, so he tried Chiropractic.
He entered the office and saw at a glance,
in a place such as this, illness hasn’t a chance.

The office staff smiled, the music was sappy,
with all of the patients contented and happy.

In a very short time, to judge by the clock,
he was in the adjusting room, talking to Doc.

It must be the hurry, the tension and all,
I simply can’t seem to get on the ball.
Life used to be easy;
just kids, toys and whistles,
now I dodge smog, spaceships and missiles.

And Doc, take a look at the size of this pack!
Have you any idea what it does to my back?
Poor Santa was miserable and just barely able,
with the help of the Doctor, to get on the table.

The Doctor was gentle;
without a fuss or a tussle
he examined the vertebrae
and relaxed every muscle.
He spotted trouble and then with a click,
started aligning the spine of old St. Nick.

Santa felt aches and pains slipping away
and in no time at all he began to feel gay.
The air was a tingle with new fallen snow
and a healthy Kris Kringle was rarin’ to go.

As he went out the door, he threw them a kiss;
why, it had been centuries
since he felt good as this!
Then once more he shouldered
the bag full of toys,
his heart overflowing with true Christmas joys.

Thanks to Allen Hoaglund, D.C. for sharing this with us all

THE NIGHT BEFORE CHRISTMAS

by Clement Clarke Moore or Henry Livingston

‘Twas the night before Christmas, when all through the house
Not a creature was stirring, not even a mouse;

The stockings were hung by the chimney with care,
In hopes that St. Nicholas soon would be there;

The children were nestled all snug in their beds,
While visions of sugar-plums danced in their heads;

And mamma in her ‘kerchief, and I in my cap,
Had just settled down for a long winter’s nap,

When out on the lawn there arose such a clatter,
I sprang from the bed to see what was the matter.

Away to the window I flew like a flash,
Tore open the shutters and threw up the sash.

The moon on the breast of the new-fallen snow
Gave the lustre of mid-day to objects below,

When, what to my wondering eyes should appear,
But a miniature sleigh, and eight tiny reindeer,

With a little old driver, so lively and quick,
I knew in a moment it must be St. Nick.

More rapid than eagles his coursers they came,
And he whistled, and shouted, and called them by name;

“Now, Dasher! now, Dancer! now, Prancer and Vixen!
On, Comet! on Cupid! on, Donder and Blitzen!

To the top of the porch! to the top of the wall!
Now dash away! dash away! dash away all!”

As dry leaves that before the wild hurricane fly,
When they meet with an obstacle, mount to the sky,

So up to the house-top the coursers they flew,
With the sleigh full of toys, and St. Nicholas too.

And then, in a twinkling, I heard on the roof
The prancing and pawing of each little hoof.

As I drew in my head, and was turning around,
Down the chimney St. Nicholas came with a bound.

He was dressed all in fur, from his head to his foot,
And his clothes were all tarnished with ashes and soot;

A bundle of toys he had flung on his back,
And he looked like a peddler just opening his pack.

His eyes — how they twinkled! his dimples how merry!
His cheeks were like roses, his nose like a cherry!

His droll little mouth was drawn up like a bow,
And the beard of his chin was as white as the snow;

The stump of a pipe he held tight in his teeth,
And the smoke it encircled his head like a wreath;

He had a broad face and a little round belly,
That shook, when he laughed like a bowlful of jelly.

He was chubby and plump, a right jolly old elf,
And I laughed when I saw him, in spite of myself;

A wink of his eye and a twist of his head,
Soon gave me to know I had nothing to dread;

He spoke not a word, but went straight to his work,
And filled all the stockings; then turned with a jerk,

And laying his finger aside of his nose,
And giving a nod, up the chimney he rose;

He sprang to his sleigh, to his team gave a whistle,
And away they all flew like the down of a thistle.

But I heard him exclaim, ere he drove out of sight,
“Happy Christmas to all, and to all a good-night.”

Autism and Christmas: Please Share Your Thoughts!

I've worked hard to make Christmas work for my child with autism.  We rehearsed greeting family, saying thank you for gifts, smiling, hugging...  but I just KNOW my sister will raise her eyebrows across the room to her husband whenever Sam says or does anything strange...  and I KNOW my mother will want to have a "talk" with me in the kitchen about how things are going and whether Sam will ever be like other kids.   And while I don't think Sam's cousins will pick on him, it's likely they'll just ignore him, or tell him to go away.  Of course, things could be worse...  but I'm dreading Christmas with the extended family!

Are you anticipating a Christmas like this one - or living through one?  What do you do to make it work for you and your immediate family?


Autism and Christmas: Please Share Your Thoughts! originally appeared on About.com Autism on Friday, December 24th, 2010 at 08:55:59.

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Autism and Christmas: Please Share Your Thoughts!

I've worked hard to make Christmas work for my child with autism.  We rehearsed greeting family, saying thank you for gifts, smiling, hugging...  but I just KNOW my sister will raise her eyebrows across the room to her husband whenever Sam says or does anything strange...  and I KNOW my mother will want to have a "talk" with me in the kitchen about how things are going and whether Sam will ever be like other kids.   And while I don't think Sam's cousins will pick on him, it's likely they'll just ignore him, or tell him to go away.  Of course, things could be worse...  but I'm dreading Christmas with the extended family!

Are you anticipating a Christmas like this one - or living through one?  What do you do to make it work for you and your immediate family?


Autism and Christmas: Please Share Your Thoughts! originally appeared on About.com Autism on Friday, December 24th, 2010 at 08:55:59.

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Online ADHD Support Group

Sometimes this holiday time of year can get fairly hectic and overwhelming. If you are feeling that you'd like a little extra support or just need to share with others who understand ADHD, please feel free to connect in our ADD/ADHD Discussion Forum.

Our Forum is an online community where people can come together from all over to ask questions, interact, and seek support from others who understand what it is like to live with ADHD as a parent, spouse, partner, sibling, or individual with ADHD. It is also a place where you can share your thoughts and ideas about what works in your family or for you as an individual, providing support to others in the process. Our online community is a place of respect, caring, and education about ADHD.

Click on ADD/ADHD Discussion Forum to visit our community.

Photo © Michelangelo Gratton

Online ADHD Support Group originally appeared on About.com ADD / ADHD on Monday, December 20th, 2010 at 22:40:06.

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Online ADHD Support Group

Sometimes this holiday time of year can get fairly hectic and overwhelming. If you are feeling that you'd like a little extra support or just need to share with others who understand ADHD, please feel free to connect in our ADD/ADHD Discussion Forum.

Our Forum is an online community where people can come together from all over to ask questions, interact, and seek support from others who understand what it is like to live with ADHD as a parent, spouse, partner, sibling, or individual with ADHD. It is also a place where you can share your thoughts and ideas about what works in your family or for you as an individual, providing support to others in the process. Our online community is a place of respect, caring, and education about ADHD.

Click on ADD/ADHD Discussion Forum to visit our community.

Photo © Michelangelo Gratton

Online ADHD Support Group originally appeared on About.com ADD / ADHD on Monday, December 20th, 2010 at 22:40:06.

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Coping With Holiday Stress

What is it about the holiday season that can be so much fun, yet so disruptive at the same time? Holidays are filled with family, love, and celebration, but they can also create quite a bit of stress - particularly for kids and adults with ADHD.

Tips for Coping with Holiday Stress

Photo © Photos.com

Coping With Holiday Stress originally appeared on About.com ADD / ADHD on Monday, December 20th, 2010 at 22:37:25.

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Coping With Holiday Stress

What is it about the holiday season that can be so much fun, yet so disruptive at the same time? Holidays are filled with family, love, and celebration, but they can also create quite a bit of stress - particularly for kids and adults with ADHD.

Tips for Coping with Holiday Stress

Photo © Photos.com

Coping With Holiday Stress originally appeared on About.com ADD / ADHD on Monday, December 20th, 2010 at 22:37:25.

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Community Inclusion v Access: What Works?

I used to really question programs set up especially for kids with autism.  The "special" days (or nights) during which ONLY kids with autism and their families would come to the zoo, skate at the skating rink, or eat at the diner.

Yes, it's easy for everyone - and it's relatively inexpensive for all.  Families with kids on the autism spectrum can go out and have fun without the added burden of curious stares, judgemental peers or worried staff.  They might even meet a few people with similar circumstances.  Meanwhile the staff of the zoo, the skating rink, the diner, etc., need no special training; all they really need to do is ensure safety, answer questions, and avoid staring.

What's wrong with that kind of a program?

Honestly, there's nothing wrong at all - except that the program, while it provides access, is utterly non-inclusive.  In essence, the message is "sure, you're welcome to partake in our offerings - so long as you do so when no one else will be disturbed or confused by your child."  And while access is a terrific first step, it leaves the person with autism - as well as his or her family - in the margins of society.

Today, I understand that access, while it isn't inclusion, is much more than most families with autistic children hope for (and much more than most community organizations offer).  And I do understand that, for many people with autism, full inclusion may be impossible under certain circumstances.  If you don't have the ability to sit still for more than a minute or two, you can't realistically attend a concert or play with a typical audience.  If you don't have the ability to communicate non-verbally, it's tough to include you on a serious sports team.   And if you're terribly sensitive to sounds, smells and tastes, full inclusion at a gourmet restaurant may not be worth the effort.

Despite all the challenges, though, many children, teens and adults with autism ARE included in a wide variety of activities.  Talented educators and coaches figure out what it takes to make their offerings work for individual people on the spectrum - and they "just do it."

We've done a lot of searching, and hit a lot of brick walls, but we've found many such talented and/or dedicated individuals and opportunities.  We've found instrumental instructors willing to take a few extra minutes to come up with creative strategies for teaching our son to play clarinet.  We've found a tennis coach who really doesn't care whether kids in the "junior" tennis group have advanced conversational skills.  We've discovered museum exhibits, drama classes, swim instructors and art teachers who - intentionally or not - find a way to make a teen with autism welcome, supported and successful.

Have you taken advantage of accessible programs for people with autism - such as special nights at the museum, special showings of movies, special afternoons at the skating rink?  Have you gotten involved with inclusive programs that make your child (and you) a part of the general program?  Share your experiences, and tell us why it worked (or didn't work!).



Community Inclusion v Access: What Works? originally appeared on About.com Autism on Monday, December 20th, 2010 at 20:02:20.

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Community Inclusion v Access: What Works?

I used to really question programs set up especially for kids with autism.  The "special" days (or nights) during which ONLY kids with autism and their families would come to the zoo, skate at the skating rink, or eat at the diner.

Yes, it's easy for everyone - and it's relatively inexpensive for all.  Families with kids on the autism spectrum can go out and have fun without the added burden of curious stares, judgemental peers or worried staff.  They might even meet a few people with similar circumstances.  Meanwhile the staff of the zoo, the skating rink, the diner, etc., need no special training; all they really need to do is ensure safety, answer questions, and avoid staring.

What's wrong with that kind of a program?

Honestly, there's nothing wrong at all - except that the program, while it provides access, is utterly non-inclusive.  In essence, the message is "sure, you're welcome to partake in our offerings - so long as you do so when no one else will be disturbed or confused by your child."  And while access is a terrific first step, it leaves the person with autism - as well as his or her family - in the margins of society.

Today, I understand that access, while it isn't inclusion, is much more than most families with autistic children hope for (and much more than most community organizations offer).  And I do understand that, for many people with autism, full inclusion may be impossible under certain circumstances.  If you don't have the ability to sit still for more than a minute or two, you can't realistically attend a concert or play with a typical audience.  If you don't have the ability to communicate non-verbally, it's tough to include you on a serious sports team.   And if you're terribly sensitive to sounds, smells and tastes, full inclusion at a gourmet restaurant may not be worth the effort.

Despite all the challenges, though, many children, teens and adults with autism ARE included in a wide variety of activities.  Talented educators and coaches figure out what it takes to make their offerings work for individual people on the spectrum - and they "just do it."

We've done a lot of searching, and hit a lot of brick walls, but we've found many such talented and/or dedicated individuals and opportunities.  We've found instrumental instructors willing to take a few extra minutes to come up with creative strategies for teaching our son to play clarinet.  We've found a tennis coach who really doesn't care whether kids in the "junior" tennis group have advanced conversational skills.  We've discovered museum exhibits, drama classes, swim instructors and art teachers who - intentionally or not - find a way to make a teen with autism welcome, supported and successful.

Have you taken advantage of accessible programs for people with autism - such as special nights at the museum, special showings of movies, special afternoons at the skating rink?  Have you gotten involved with inclusive programs that make your child (and you) a part of the general program?  Share your experiences, and tell us why it worked (or didn't work!).



Community Inclusion v Access: What Works? originally appeared on About.com Autism on Monday, December 20th, 2010 at 20:02:20.

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MDs Admit Low Confidence In Diagnosing Musculoskeletal Complaints in Children

A recent study, published in the Journal of Pediatrics, details the results of sending questionnaires to a broad spectrum of British medical providers (practicing in Primary Care, Pediatrics, Emergency Care, and Orthopedics management). These doctors were asked to self-rate their confidence in pediatric musculoskeletal clinical assessment.

The depressing results are that 73% of these doctors graded themselves as having “low” to “no” confidence in their pediatric assessment skills. [1]

Considering that musculoskeletal complaints are the primary reason that parents bring their children to a medical provider [2], it’s no wonder that more and more parents now bring their children to the undisputed leader in NMS management…chiropractors. [3]

REFERENCES:

1. Doctors Likely to Encounter Children With Musculoskeletal Complaints Have Low Confidence in Their Clinical Skills
The Journal of Pediatrics 2009 (Feb); 154 (2): 267–271

2. The Safety and Effectiveness of Pediatric Chiropractic: A Survey of Chiropractors and Parents in a Practice-based Research Network
Explore (NY) 2009 (Sep–Oct); 5 (5): 290–295

3. End Medical Mis-Management of Musculoskeletal Complaints
A ChiroZINE Editorial

Trading Backpacks For Rolling Luggage Fails in German Primary School Study

It’s well understood that heavy backpacks are taking a heavy toll (excuse the pun!) on adolescent spines. [1] A recent standing magnetic resonance imaging study by the Department of Orthopaedic Surgery, University of California, at San Diego revealed that: “Increasing backpack loads significantly compressed lumbar disc heights measured in the midline sagittal plane” and that: “student subjects reported significant increases in back pain, associated with increasing backpack loads from 4, to 8, and finally to 12 kgs of carried weight”.

The most recent novel study was performed with German primary school children. [2] The researchers wanted to determine whether giving the children rolling luggage to carry their school books might reduce spinal stress. As it turns out, what might work well for Mom at the airport does not work so well for Junior, lugging his books across uneven sidewalks on the way to school. The authors had to conclude that: “This suggests that school children should use backpacks rather than trolleys when the weight is within recommended limits”.

REFERENCES:

1. The Backpacks and Children Page
www.chiro.org/LINKS/backpacks.shtml

2. Comparison of the Posture of School Children Carrying Backpacks Versus Pulling Them on Trolleys
Clinical Chiropractic 2010 (Dec); 13 (4): 253–260
www.chiro.org/LINKS/ABSTRACTS/Comparison_of_the_Posture.shtml

Chiropractic’s Next Battle: AMA Ownership of the CPT Codes

SOURCE: Dynamic Chiropractic ~ Dec 16, 2010

By Donald M. Petersen Jr., BS, HCD(hc), FICC(h), Publisher

As 2010 comes to a close, it is important to look ahead to see what we can do as a profession to brighten the future of chiropractic. Among the many bits of information that have come across my computer monitor of late is a very interesting article by John Weeks of The Integrator Blog, “an organizer-writer in the emerging fields of complementary, alternative and integrative medicine since 1983.” [1] The article points out that the American Medical Association (AMA) has owned the current procedural terminology (CPT) codes for more than 40 years.

The benefits of this ownership are probably much greater than you realize. Basically, they amount to the following:

  • Control:   By owning the CPT codes, the AMA effectively keeps a lid on what doctors of chiropractic (not to mention nurses, optometrists, acupuncturists, doctors of naturopathy, etc.) can be reimbursed for. None of the other health care professions is able to create new codes that are more reflective of what they do (and should be reimbursed for) without saying “AMA, may I?”

  • Influence:   By controlling the CPT codes, the AMA is able to influence health care policy decisions on a national level through its relationship with the U.S. Department of Health and Human Services, particularly with the Centers for Medicare & Medicaid Services. This ultimately translates into undue influence with third-party payers who are unlikely to jump over the CPT code barrier to explore more efficient care options from non-medical providers.

  • Money:   Weeks estimates that the AMA’s CPT-related income is approximately $71 million per year. Not a small chunk of change considering that their membership dues (from less than 20 percent of licensed MDs) is less than $44 million. Here is AMA’s income breakdown for 2009 [2] (unfortunately, the CPT-related income is not able to be broken out): membership dues $42.3 million; advertising $23.4 million; periodical subscription revenues $12.7 million; other publishing revenue $19.3 million; books, newsletters and online product sales $50.0 million; royalties and credentialing products $66.4 million; insurance commissions $34.0 million; investment income $9.6 million; grants and other income $10.6 million; and other $0.5 million.

The most important point to all this is what the AMA does with the $71 million of CPT-related income each year. The AMA typically spends between $15 million and $22 million in direct lobbying each year, something it refers to as “advocacy.” Much of that lobbying money is spent to keep chiropractic and other non-medical professions in their place. Add to that “marketing and communications” spending that runs between $13 million and $27 million each year, and almost $50 million is spent each year to advance the AMA agenda.

Other probable uses for the money include the Scope of Practice Partnership (SOPP) campaign that began in 2006 and continues today. [3] The Scope of Practice Partnership is designed to oppose any effort by any other health care profession to expand their scope into areas where the AMA doesn’t want them.

Interestingly enough, the genesis of Weeks’ article was a question from integrative nursing leader Mary Jo Kreitzer, RN, PhD, who founded and directs the Center for Spirituality and Healing at the University of Minnesota. What makes this interesting is that chiropractic is not the only profession looking at the unfair advantage the AMA has established with its continued ownership of the CPT codes. This battle could help us build some exciting alliances with a number of professions, particularly the nurses.

To close, I would like to offer the “recap” from Weeks’ article, as it does an excellent job of presenting the important points. In the article, he refers to the various health care professions as “guilds”:

  • “All guilds must use the CPT if they want to participate in 3rd party payment.

  • To do so, they must pay one guild, the AMA.

  • This guild is pitted against their efforts to expand their practice scopes.

  • In addition, this guild is apparently opposed to multidisciplinary recommendations from the brains of US medicine about the future of healthcare in the United States.

  • As is clear in the IOM report, many medical doctors are not aligned with the AMA position. In fact, the AMA that received these $71-million+ each year presently counts only 15%-20% of MDs as dues-paying members.”

As I look at our horizon, I can see no better opportunity for this profession to break the bonds of the AMA’s hold on the chiropractic profession (and all other health care professions) than through breaking their grasp on the CPT codes.

References

1.   Weeks J. “The AMA’s $70-Million Taxation Without Representation: Is It Time for a ‘CPT Party’ Royalty Revolt?
The Integrator Blog ~ Wed, Oct 20, 2010

2.   American Medical Association Annual Report, 2009

3.   “AMA Scope of Practice Partnership Tightens Its Grip
Dynamic Chiropractic, Jan. 15, 2007

Study’s Conclusion: Living Near a Freeway Associated With Autism

A group of highly-regarded researchers at UC Davis's CHARGE (Childhood Autism Risks from Genetics and the Environment) conducted a multi-year study to determine whether effects of air pollution are likely to have an impact on the incidence of autism.  Today, they have published findings that suggest an association between autism and proximity, during the third trimester of pregnancy, to freeways.  It's important to note that the study does NOT provide any insight into what specific pollutant, if any, could be responsible for a higher rate of autism.

Here is the abstract from the report:

Background: Little is known about environmental causes and contributing factors for autism. Basic science and epidemiological research suggest that oxidative stress and inflammation may play a role in disease development. Traffic-related air pollution, a common exposure with established effects on these pathways, contains substances found to have adverse prenatal effects.

Objectives: To examine the association between autism and residence proximity, during pregnancy and near the time of delivery, to freeways and major roadways as a surrogate for air pollution exposure.

Methods: Data were from 304 autism cases and 259 typically developing controls enrolled in the Childhood Autism Risks from Genetics and the Environment (CHARGE) Study. The mother's address recorded on the birth certificate and trimester specific addresses derived from a residential history obtained by questionnaire were geo-coded and measures of distance to freeways and major roads were calculated using ArcGIS software. Logistic regression models compared residential proximity to freeways and major roads for autism cases and typically developing controls.

Results: Adjusting for sociodemographic factors and maternal smoking, maternal residence at the time of delivery was more likely be near a freeway (≤309 meters) for cases, as compared to controls (odds ratio (OR), 1.86, 95% confidence interval (CI) 1.04-3.45). Autism was also associated with residential proximity to a freeway during the third trimester (OR, 2.22, CI, 1.16-4.42). After adjustment for socio-economic and demographic characteristics, these associations were unchanged. Living near other major roads at birth was not associated with autism.

Conclusions: Living near a freeway was associated with autism. Examination of associations with measured air pollutants is needed.

This study is by no means the first to associate autism with pollution or toxins.  Pesticides, pet shampoos and emissions from coal burning  plants have all come under scrutiny.  What makes this study particularly significance is the quality of the researchers, the size and scope of the study, and the fact that the numbers were adjusted for several possible confounding factors (socioeconomic and demographic status).  This might suggest that an earlier study which linked higher socio-economic levels to autism may relate more to location than to genetics - though of course the study did not look at this issue, and my thoughts about it are simply speculation.

More Articles on Causes of Autism


Study's Conclusion: Living Near a Freeway Associated With Autism originally appeared on About.com Autism on Friday, December 17th, 2010 at 07:08:11.

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