Sunday, April 21, 2013

Update: "Vaccines Not Associated With Autism"

Update on 4/21/13:

There is a very interesting discussion in the comments section of the Left Brain Right Brain, LBRB website, linked below, in a topic  where Matt Carey went through the historical element of this Vaccine Controversy along with the expression of disgust that exists among some people, associated with Andrew Wakefield and the recent outbreak of Measles in Europe.

There is good information in that discussion for anyone who may be considering Temple Grandin's recent recommendation on her website, in consideration of a delay in MMR vaccination to age 5, if there are familial vulnerabilities that Grandin identifies on her website, in what looks like a quote from her upcoming book, "The Autistic Brain". 

I support what I see as reasonable aspects of her concerns, in the comments section of the discussion linked below; however, in the discussion, I provide the evidence that I am able to locate and link, which still leans heavily toward the benefit of vaccines over the cost of potential rare side effects, even if some of the general vulnerabilities of neurology and health that Grandin identifies, exists per family history. 

My personal opinion that continues as it has been the same in the past, is that only a physician is qualified to determine what type of Health Vulnerability in each unique case is worthy of consideration on a decision whether or not to vaccinate. 

Where there is no health vulnerability assessed by a physician, all the available evidence that exists shows that the benefits of vaccination greatly outweigh the potential costs in risk of side effects that have been studied, identified, and assigned statistical risk in percentage, updated in 2012, as detailed in the discussion, linked below from the LBRB website.

I appreciate Matt Carey, allowing me to participate in the discussion, as a relative Layman on these issues, whereas some of the other individuals discussing the issue appear to have been focused on it for years. 

I do not share the same level of emotional investment that some of the other people in the comments express; however, on the other hand, I am not versed in the level of detail some others have by memory, so it is a research project for me in real time, where I stumble on some of the "vaccine related jargon" that I correct in my comments in the discussion.

In addition, Temple Grandin's website is linked below for those who wish to review the comment that I referenced from her, on that website.

www.templegrandin.com




http://leftbrainrightbrain.co.uk/2013/04/17/andrew-wakefield-dont-try-to-blame-me-for-the-results-of-what-i-said-and-did/

Original Blog Post from "Vaccines Not Associated With Autism" on 3/30/13:


 

The headline provided by the CDC, in the linked article below, specific to the described study states: "Vaccines not associated with Autism".

Regressive Autism is the only significant subgroup of autism that is the topic of parental observation of concern with vaccines, in the broad autism spectrum and the much broader autism phenotype.

http://www.cdc.gov/vaccinesafety/Concerns/Autism/antigens.html 


This study did not prove there was no association of vaccines with Autism. Specific to the vaccine concern and regressive autism, what it did provide evidence for, as quoted from the article, was this:

"Children with ASD with regression (the loss of developmental skills during the second year of life) did not receive an increased number of vaccine antigens when compared to children without ASD with regression."

This was only an analysis of regressive Autism as defined in the loss of developmental skills during the second year of life, which may have a number of different underlying contributing factors depending on the type of regression.

The regression was not defined specific to loss of language skills, so it is difficult to assess the specific characteristics and severity of the regression, in the sample of 49 children studied. A similar limitation was addressed by Matt Carey, in 2009, in the LBRB blog linked below when an association of Mitochondrial disease, fever, and Regressive Autism was suggested in research. In that study, greater detail was provided in how Regressive Autism was defined than the CDC topic study.
 

http://leftbrainrightbrain.co.uk/2009/09/24/fever-plus-mitochondrial-disease-could-be-risk-factors-for-autistic-regression/
 

Regressive Autism includes a spectrum of specific symptoms and differing severity levels that were defined in the study. There are a number of potential contributing factors for regression.

For one, Hyperlexia is associated with regression in language, and that general condition is estimated in about 5 to 10% of cases of Autism. Another potential contributing factor of risk for regressive Autism is abnormal brain growth associated specific to males with Autistic Disorder.

It is not clear what the direct causal factors are in any of these conditions but there is growing evidence for identified associations that may play a role as contributing factors of risk. What is known about vaccines and identified in the link below, by the CDC, is that there is a risk of fever severe enough to cause seizures in about one out of every 3000 that are vaccinated.

http://www.cdc.gov/vaccines/pubs/vis/downloads/vis-mmr.pdf


There is recent research, as linked below, that seizures, language and motor development in Autism are potentially associated and linked in genetic mutations in duplications of chromosome 15q11-q13, in 1 to 3% of spectrum disorders.

http://www.sciencedaily.com/releases/2013/03/130326101532.htm

One can consider that Autistic Disorder, alone, is currently defined very loosely at this point in time, where 2027 potential combinations of behavioral impairments and/or developmental delays technically could result in a diagnosis where 2 people could be assessed with Autistic Disorder without any intersection of behavioral impairments.

http://crackingtheenigma.blogspot.com/2011/02/exactly-how-many-ways-are-there-to-get.html

It is beyond reason to suggest that one underlying factor could be responsible for Autistic Disorder, considering the complexity of how it is currently defined as a disorder. PDDNOS is currently defined loosely enough by DSMIV standards that a diagnostic tool used to assess PDDNOS in recent research conducted by Catherine Lord and associates, as described in the analysis in the link below, provides a suggestion of a potential misdiagnosis in up to 90% of those assessed in a "non-autistic" group of individuals studied.


http://crackingtheenigma.blogspot.com/2012/10/more-dsm-5-confusion.html


At this point in time, the DSMIV guidelines describe an Autism Spectrum of Disorders that could be associated with almost any factor, including being alive, at least per the diagnostic tool used in Lord's study. It has never been too early to suggest that Vaccines are not the definitive Cause of Autism.

However, it is much too early for the CDC to suggest that there is no association, from this very limited study and the research that has been done to this point. For whatever reason, as provided in research by the CDC, in one out of 3000 people vaccines trigger a side effect of high fevers and seizures. At this point, they do not have clear evidence for why it happens, but it happens.

This is a common issue in many side effects of pharmaceutical intervention. I suspect that if identical research was done in an attempt to disprove that seizures are associated with exposures to greater numbers of antigens from vaccines, that the results would be the same. However, if so, it would be incorrect to suggest that seizures are not associated with Vaccines. They happen. They just don't fully understand why.

It is rare that this happens, but it is also not well understood at all what the actual percentage of children with regressive autism that get severely ill after vaccines are. There is no way to objectively assess that other than a parental survey. However, in rare cases, some children do fall severely ill, and behavioral symptoms of Autism do become more noticeable leading to diagnosis. It happens. They just don't fully understand why.

The underlying factors of seizures cannot always be assessed in an individual. However, the symptoms can be measured by behavior or EEG, when there are no structural anomalies in neurology that can be assessed. There are no clues but behavior in many individuals currently assessed with behavioral impairments associated with ASD's.

At least up until this point, much of the problem in assessing what the causal/contributing factors are is poor diagnostic guidelines that have been used to define what Autism even is, as a neurodevelopmental behaviorally assessed condition.

With DSM5 standards and ICD11beta revision to date, Autism becomes a core behavioral impairment in reciprocal social communication. There is currently no one defined impairment that can be measured by either neurological or behavioral assessment that is core to all Autism Spectrum Disorders, in either DSMIV or ICD10 guidelines, so there can be no potential of one core definitive causal factor. Not even five. Not even 10.

As long as there is the potential of a contributing factor of seizures and potential brain damage, no matter what the underlying factor of the seizures may be, there is the potential of some association. However, at least at this point, per the research that exists, it does not appear to be a potential contributing factor in more than 1 to 3% of the spectrum.

That may not sound like many people but it could comprise 20 to 60K individuals currently estimated as diagnosed, under the loose criteria that exist now. The topic study does not come close to disproving that potential rare association, however small it may be, as a contributing factor.

As a comparative gravity of issue, there were about 7 people that participated in a flash blog that got the attention of a large charitable organization recently, per concern over how the organization describes people on the spectrum in a video about AAC. However, this article, in that same charitable entity's delivery of the research, as communicated here, received much greater amounts of outrage from parents that witnessed their children falling ill after vaccination with observation of greater behavioral impairments after that point. It happens. They don't clearly understand why.

Nevertheless, it understandably, still, is an issue of concern among those that witness this serious issue in their children, in rare cases when it happens. There might not be so much fear of government conspiracies, if the CDC could just state at this point they don't know why this happens as a potential side effect in rare cases after vaccinations. It is reported. It happens.
 

It is much more common than death following a vaccination but potentially less common than one out of 3000 severe fevers and seizures as a side effect of a vaccination. Additional effort at research addressing potential root associations such as genetic mutation, fever, seizures, mitochondrial disease and Autism could still provide additional answers.

However, at this point, a general assessment in a statement of no association by the CDC is not much more believable than a statement of definitive causation. At least, for the limited number of individuals that has witnessed increased observable impairments associated with Autism, happening in their children after vaccination.

It makes it sound like there are many people complaining about it if one limits their world to online resources, but the potential contributing audience, online, is one of global nature and millions of people. It is a similar issue as a couple of hundred people online taking offense at a compassionate portrayal in a video about AAC.

In the real world, it is not on the radar for most people. There are more people listening to the anti-vaccine rhetoric of Alex Jones in the US, than has been attributed to people like Jenny McCarthy. However, in the US, the CDC is doing a great job of promoting what is the overall benefit of vaccines as a lifesaving effort, as the US retains levels close to the highest it has had in the past in "Herd Immunity" in the population at about 95%.

Religious waivers are still the greatest area of refusal to vaccinate other than medical reasons. This is one area, overall, in the US, per society adherence to the medical model of disability, in advantage in keeping the population healthy. The US was hardly phased by the Wakefield Vaccine/Autism research, whereas in Europe there was a substantial causal effect associated lowering the assessed vaccination rates below "herd immunity" in 80-percentile territory.


For anyone that made it this far, in this compiling of data, in two of my blog posts here is an additional avenue of potential interest. :)


The Autism Research Scientist that writes in the Blog linked below provides a virtual "Goldmine" of resources addressing the Co-morbid conditions associated with what is currently described and defined as the Autism Spectrum under DSMIV guidelines.

In regard to GI issues and Autism, and all the research that is coming out now, that is farther removed from the "vaccine controversies", this Autism Research Scientist's post linked here and the comments on it, provide an excellent overview of the state of science on this issue of GI difficulties and Autism, leaving the "vaccine controversies" in the dust, so to speak.

All of the blogs he lists on his blogroll are worth taking a look at when one who is interested in this kind of science, has the time.

http://questioning-answers.blogspot.co.uk/2013/03/gastrointestinal-mucosal-molecular-profile-autism.html



Autism, the Internet and "Ideological First Identity", a Collection of Thoughts:

http://katiemiaaghogday.blogspot.com/2013/05/autism-internet-and-ideological-first.html







"AutisticS Peeks!"


It's Good

to Hear

ya
:)!
*


(:@@
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!*




AS
P:

Autistic Spectrum
Perception

and

Perspective


Thursday, April 18, 2013

Continuing Challenges in Online Autistic Communication


Helping Others Understand Me Better:

                                                  


If I had all the answers, I would not pursue brain storming sessions with others.

I found the low prevalence of ASD, in door-to-door Scans in Amish Counties, intriguing since about a half a year ago, when I read the study. I do not claim to come close to know all the reasons and I do not experience Autism the way many others do as currently assessed by DSMIV criteria.


The person that got me thinking about this before I found the study was a Motorcycle Biker and Deep Thinker that often visits this site. He Brain storms better than any person I have come across in writing. His user name is [name redacted].

I suspect there are many more on this site. That hypothesis has already been confirmed, at least for me.

Yes, you are correct, this issue is much more complicated than social roles and social stimulus; however, that was a point I felt I could start on that everyone could agree on. Other than that, I am not sure how many more words or how many more ways I can find to confirm that yes I do realize I am not a good social communicator nor am I usually artful in the use of "colloquial terms".

"What you See is What you Get", and in my case it is "more or less" an "advanced form of Echolalia", mixed with "Google" and "a sprinkle" of "Human Algorithm" that comes from every source imaginable, at least for me.

Some of those "colloquial terms", are mine alone, which "in effect" makes them "oxymorons".

In conclusion, it is hard to make a "Human Algorithm" angry.

However, they can learn to say thank you and apologize.

It seems through your written communication I am making you angry from my communication style.

I apologize for that offense not intended. To be as honest as a "human algorithm" can, at least in my case, I have no idea why you continue to seem to be angry from my form of communication here.

Thank you, in advance, for understanding that, if you can.
 




Coming To Understand Others Better:
                                                
                    


 

You are very welcome [name redacted].

I exercised the privilege you have allowed me to like things on your page. In addition, as sometimes happens with RRBI's, once I got started I could not stop. By the time, I got to January, 19th, the "Facebook Algorithm Social Police" told me, "enough you cannot do that anymore".

I do not get very many likes on my pages, and I recognized, oh gosh, this probably is piling up in your notifications 'cause I liked at least 200 items if not 500.

In my journey of "Facebook liking" things on your page in the last three months, and then viewing everything on your page back to when you started I came to some "a-ha moments".

One was an apology I recognized I do you owe you for not thanking you enough and complimented you enough on all the positive things you do on your page.

I suppose part of that was my personal page was completely private and I did not realize that the owner of the page was actually notified of likes.

I think I "Facebook liked" at least 90% of what I saw on your page. I feel bad about that because I didn't know how to put it into words to tell you in the comments, before, and I guess that is the whole purpose behind "likes", in the first place, for people just to show appreciation and thanks, in reciprocal social communication.

I did not understand that until a person asked to be my friend on Facebook.

Additionally, for what ever reason, 99% of the things I remember I disagreed with are gone. What is left is this amazing expression in "Art of Acceptance" of people on the spectrum. It is like the book you illustrated, but it is illustrated with real lives and real stories from people across the spectrum.

There is only one word I can adequately use to describe the feeling it gives me to take the journey from now until the start of your page.





Joy.


I am sorry I was such "a pain in your ***".  In addition, yes I do literally recognize now how much of  "a pain in the ***" I was. Particularly, considering I never let you know how much I liked the positive things on your page.

I want to tell you thank for what you do. However, I also what to sincerely tell you thank you for banning me when you did, because it inspired some spark of creativity in me that I did not have before. I now have a voice of my own, that I never had before. I literally owe that to you.

I understand Facebook better now, and a few people are actually interacting with me. However, it wasn't just the banning, and was the least of what inspired me. It was all those emotional pictures and expressions of humanity on your page that helped me get in touch with something inside me that I had difficulty finding.

It is no wonder you have over 25K likes on your page.

Your friend,
Katie.
                                                    



Two examples of challenging topics in Online Autism Communities in building bridges of communication between people off and on the spectrum linked here in these two discussions:


https://www.facebook.com/thinkingpersonsguidetoautism/posts/530675340307131


https://www.facebook.com/thinkingpersonsguidetoautism/posts/573252269359780


A link to a recent discussion among people on and off the spectrum, ending on 5/15/13, which was particularly challenging in "Reciprocal Social Communication"; the core defined challenge of being on the Spectrum:


https://www.facebook.com/thinkingpersonsguidetoautism/posts/536514663056532




I finally found someone Online who has Actual Effective Answers to improve Online and Offline Reciprocal Social Communication Among People On and Off the Spectrum.

He is also a Champion in providing Actual Effective Answers to Improve Positive Awareness and Acceptance for ALL people on and off the Spectrum.

Bill from the "Autism Discussion" Facebook Page!

He is one of the most "non-biased" people I have come across, On or Off the spectrum, as a 100% Autism Advocate and REAL Ally of Everyone.

Here is the link to his Facebook Page:

https://www.facebook.com/autismdiscussionpage


And here is a link to the Discussion I started on the Wrong Planet website, where I used the metaphor of  "Wired Differently Whisperer", to direct attention to the helpful resources on his Facebook Page. :)

http://www.wrongplanet.net/postt231214.html


Autism, the Internet and "Ideological First Identity", a Collection of Thoughts:

http://katiemiaaghogday.blogspot.com/2013/05/autism-internet-and-ideological-first.html







"AutisticS Peeks!"


It's Good

to Hear

ya
:)!
*


(:@@
@:)
!*



AS
P:

Autistic Spectrum
Perception

and

Perspective


Saturday, April 13, 2013

The "Broader Amish Autism Phenotype" vs. "The Autistic Matrix"



There is a 1 in 271 prevalence of Autism Spectrum Disorders reported in two Amish Counties in a door-to-door screen, from preliminary results of a study in 2011, as opposed to the 1 in 50 prevalence in the rest of the US, from a phone survey of parents for children actually diagnosed, a recent study supported by the CDC.


https://imfar.confex.com/imfar/2010/webprogram/Paper7336.html

http://www.cdc.gov/nchs/data/nhsr/nhsr065.pdf

Autism is diagnosed as not only symptoms characteristic of the condition, but also as one that impairs one in a major area of life functioning. Acceptance is an ongoing issue in daily life that changes by the moment depending on who one is dealing with.

One cannot demand acceptance from one that chooses not to provide it, except when there are carrots and sticks that others yield to in response. People often act as if they accept their supervisors or other authority figures, but it does not mean they feel that way inside.

I suspect that people on the spectrum are more likely accepted by others, in Amish Counties and contribute greatly to society, as there is often enough to do to keep everyone busy for basic survival. Along with enough social roles to fill in a close knit society.

People in Amish Counties often do not do well in the larger world when they leave there to join the rest of the world.

It is more likely the social stress of the larger world, which makes characteristics on a much broader autism phenotype, 30 to 45 million people just in the US, observed in every country and small culture in the world, a diagnosis in some cultures verses a continued broader autism phenotype in others.

It is also potentially part of the reason that some folks, who are being diagnosed at 40 now, would likely be diagnosed at 20 now if born 20 years later because the social demands of this fast paced chaotic culture, now exceed capacity for fuller social adaptation.

People do not usually get a diagnosis, unless they are having substantial problems adapting. They often remain on that broader autism phenotype.

The DSM5 now defines Autism as symptoms of a broader autism phenotype that occur in early childhood but may not fully manifest as symptoms of an actual diagnosed condition until social demands exceed social adaptation.

Every child, later diagnosed with Autism, starts on a broader autism phenotype first.

There can be many associated factors that lead to the actual diagnosis, including superficial issues such as how the condition may be defined, how it is subjectively assessed, and awareness and accessibility of health care leading to a diagnosing professional.

I do not think it is practical to use the term Autism for online communities. I like the phrase "neurodiversity communities" as a place where every person who feels "neurodiverse" can feel free to interact with others with an almost unlimited number of neurological differences.

That is already the effective reality anyway, as many people have not made it to the point, where they feel the need or have access to healthcare to move from broader autism phenotype to actual diagnosis.

That is as long as everyone is welcome, as is the case most often on some websites, like the Wrong Planet website, where people do not find themselves in the same larger world trap of unspoken political/social ideologies they are not accepted for unless they comply and conform.

I think in Amish counties, overall, it is an issue of effective opportunity for and resulting social adaptation, which is often associated with acceptance from others.

I think that overall that is what all social animals look for in life.  I do not generally observe people on the spectrum as anti-social animals.

I think it is possible to legislate greater opportunities for social adaptation through employment and laws like the ADA. However, acceptance more often depends on social adaptation, which does not necessarily mean being a "social butterfly", as much as finding an environmental niche in a role to play as some type of contributing player.

People are having a harder time adapting, so overall society is not working, as it should, at least for those who are having trouble adapting.

Things are getting better for those most severely impacted by co-morbid medical conditions, but that is only a piece of the overall adaptation pie that exists from birth to death. The other pieces do seem to be harder to find for some now than they used to be.

The result of that is the expansion of people identifying with Autism as a source of online acceptance. That expansion currently, is not effectively inclusive enough for everyone looking for that acceptance on a much broader autism phenotype or what others refer to as "neurodiversity".

This is a potential source of conflict that exists between some parents of children on the spectrum and other people identifying on a spectrum. They are most often on the same team of a broader autism phenotype, and at times cannot clearly see that commonality, in each other.

Additionally, they are most often looking for the same thing for themselves, support and acceptance. That will probably eventually change for the better online, as the basic opportunity for social adaptation and acceptance in the "real world" does not appear to be moving in a positive direction.

The Sequester is near evidence of that future. So is increasing avenues of online participation among those identifying with Autism as not just a diagnosis, but also a way of life.

I think it is unfortunate the potential reasons why the prevalence rate of Autism is much lower in Amish counties cannot be fuller explored by research, because, at least in part, it has become politically incorrect to do so, over the unwarranted vaccine concerns.

I think this type of research could go a long way in helping people on the spectrum. I provided that comment in the last congressional oversight hearing, as a written one, but the results of that hearing in the continued focus on unwarranted mercury fears, continues to drown some of the valid concerns and efforts that could potentially help people now.

I believe that offline connections, which do not currently do well past support groups in large cities, are the first step to a larger "real life" community of people on the spectrum. However, I think that part of the reason that the offline connections do not happen, is because the opportunity for online ones continue to expand dramatically.

In addition, this certainly is not an issue specific to people on the spectrum.

Most ironically, it could be part of the overall issue of what leads to a diagnosis in the real world for some, moving from that broader autism phenotype to a diagnosed spectrum.

It is in some ways potentially a "catch 22" situation.

I had offline connections with people on that broader autism phenotype through most of the course of my life through school and work.

There were no labels then, however as I look back those people were always there. Those same opportunities I had in my historical field of work I could depend on with job security no longer exist.

For many reasons, my field of work was a magnet for people on that broader autism phenotype that one could observe nationwide. Effectively, my workplace was a "Neurodiversity Community".

One of my co-workers did the "flapping stim", where my "stim" was a religious routine of vigorous exercise.

I never made the connection in his "flapping" and my exercise routine until it was pointed out as a “stim” that some people on the spectrum share.

There is no description of "flapping" in any diagnostic manual. The only place one can usually find a description is in online autism communities. Alternatively, as was in my case, a real life observation in my "Neurodiversity Workplace".

I never came across anyone "flapping", in school that I can remember.

The people have not changed that much but the opportunity for "Stims" has. The idea of sitting still was horrifying to me in the workplace, behind a desk job, as I was hyperactive, now identified as ADHD.

I might have eventually "flapped" too, as when I was finally trapped behind a computer; I had to do push-ups to release frustration and tension, and eventually succumbed to problems with hypersensitivity to light and sound.

In trying to explain that to an elder co-worker, also obviously on a broader Autism phenotype, her response was stress does weird "s**t" to you.

There is now research that shows dysfunction of the stress response and adrenaline associated neuro-hormones, is associated with sensory integration problems.

I think this is part of the issue for people who are young that are under a level of chronic stress that I cannot imagine in a rural town, with a short walk to a small school, without even stimulation from a TV set.

For all practical intents and purposes, I grew up in something similar to an Amish County, and my ancestors more so.

That is how culture used to be for thousands of years.

People were closer to the earth in hunting and gathering, and/or agriculture. The old order of "Agri" Culture is in many ways like Amish Culture.

Some of the answers seem blatantly obvious to me because I have experienced so many different perspectives in just one life.

People now are often born in to an environment of one full serving of cultural complexity on one plate. The yearning for a place where people can successfully adapt is at the crux of many of the problems of modern civilization, I think, and again this is certainly not an issue specific to Autism.

"Tom Sawyer" by Rush:




http://www.youtube.com/watch?v=ANiaZvdGO8U                                              
                                                    


However, I do think that some people on the spectrum are among the effective "Canaries in the Coal Mine", per inherent propensity toward these greater difficulties in this type of new required social/environmental adaptation.


"Canary in a Coal Mine" by The Police:


                                                                          
http://www.youtube.com/watch?v=HnwFKwdvX78                                                    

 

With that perspective taken, the discussion from the "Wrong Planet" website related to this issue linked below is in some ways a cautionary tale for the rest of society. Some people in that discussion may be among those singing the song of the "Canary in the Coal mine".

In this event, not a noxious gas or vaccines are the offender.

It is a way of life, at least in part, that people are attempting to escape that they are "virtually" trapped in, per "Catch 22", in what is becoming an effective life that is "Matrix", in nature, for some.

 http://www.wrongplanet.net/postt224454.html


              
                     Stimulus, Chaos, and Search for Social Roles:




http://www.youtube.com/watch?v=CH1XGdu-hzQ


Balance, Structure, and Clearly Identified Social Roles:



http://www.youtube.com/watch?v=LX153eYcVrY

 
Forecast for the Future?


http://www.youtube.com/watch?v=nIZ04AGTjHc
 

Continued Discussion and Informal Poll from the Wrong Planet website linked here:


http://www.wrongplanet.net/postt228582.html



Autism, the Internet and "Ideological First Identity", a Collection of Thoughts:

http://katiemiaaghogday.blogspot.com/2013/05/autism-internet-and-ideological-first.html






"AutisticS Peeks!"


It's Good

to Hear

ya
:)!
*


(:@@
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!*




AS
P:

Autistic Spectrum
Perception

and

Perspective



Thursday, April 11, 2013

The Bing Algorithm Continues to Misbehave


Autistic Algorithm Saga Part 2:

[name redacted], to put that issue in perspective, there were seven exact phrase search results on the "Autistic People should be killed" exact keyword phrase search, before the attention given it by the online "Autism Community", in a Google Search. That is documented.

Now there are 21,900 actual Google Search Results directly as a result of people online in the Autism Community actually talking about the exact phrase, in a rhetorical instead of ill intentioned way.

There are 7,200 actual Google Search Results for the exact phrase search "Autistic People Should Be Loved", largely as a result of Landon Bryce creating a Facebook Page with that exact page title. (Cool page by the way; one of my few favorite likes I recommend on my Facebook pages).

People on the spectrum have effectively been talking about the first negative phrase in rhetorical content in Google Search Results at a rate three times higher, than the much more positive phrase.

The Microsoft Corporation owns Bing as a Search Engine. That corporation does not answer to Google's Auto Complete search specific policy.

Bing gets thirty percent of overall search engine traffic, and all of Facebook Search Engine Traffic that caters to over a billion people in the world.

It is not likely the Microsoft Corporation is ever going to yield to this kind of demand, because they cannot equally or possibly meet the potential demands of all their other Customers.

Those business efforts go well beyond the search engine part of the business where similar concerns could exist for the thousands of other disability/disorder/condition/difference "hate speech" results in a auto-complete search generated by an algorithm working on variables that also include actual "exact phrase" search results that never existed before.

Now, instead of seeing a auto-complete search generated by an Algorithm looking for random keywords in search results, people can actually go to over 20K search results on the internet to actually read about it instead of just seeing a random auto complete result that goes nowhere, of significant interest, in only seven "exact phrase" search results.



"I Robot" by the Alan Parsons Project:

 


http://www.youtube.com/watch?v=X0eKemjFz44


This is one of those things in life that cannot likely be improved on further that may be worth ignoring in the future; effectively going away for most people forever when they forget about it, focused on other pressing issues in life. Back to a time and place similar that existed before anyone randomly came across and noticed the phrase in the first place, in a auto complete search result.

However, I expect to continue to hear about the issue for sometime to come, which personally I have no problem over, because it has become another one of many special interests for me, in a world of Algorithm driven information.

The Facebook Algorithm notifies me when I'm exhibiting autistic-like behaviors, but it doesn't do any good for me to get "Mad at Math". :)

Hopefully, my comment here is a little more lighthearted than my last several comments/posts. :)




Autism, the Internet and "Ideological First Identity", a Collection of Thoughts:

http://katiemiaaghogday.blogspot.com/2013/05/autism-internet-and-ideological-first.html







"AutisticS Peeks!"


It's Good

to Hear

ya
:)!
*


(:@@
@:)
!*




AS
P:

Autistic Spectrum
Perception

and

Perspective


Autism and Unwarranted Fear Based on Label Alone


I commented on an article shared on the Facebook Version of this blog, regarding the continued myth about Society in General, typing in Hate Speech in Google Searches associated with the disability first identifying language in use of the terms "Autistics" and "Autistic People".  It is repeated here for those that do not interact with Facebook. People on the Spectrum have enough to deal with in real life, without a myth generated that society is busy away typing in identify first disability language in Google searches, to hate people on the spectrum.

Society overall, does not use the phrases "Autistic People" or "Autistics Should". Society uses the phrase "People with Autism", as it is politically incorrect to use disability first language.

That is certainly not an advertisement from me suggesting that people in described online "Autism Communities", should not use disability first language if that is their own personal preference.

However, people first disability language is the reality for most of the rest of Society. What is moreover evident, is that people first disability language for "People with Autism Should", brings up no "hate speech" and never has.

This is not the same though for "People who are fat should". They are the ones that are hated much more over those words in a actual Google Auto Complete search result, with no defined label of disorder or disability.

Most often a difference that can be visually seen in the mind's eye is what usually leads to actual hate speech results in a Google Auto Complete search that actually leads to real world results on the Internet.

Autism does not have a visual image of significance for hate to be based on label alone, overall in society.

For the most part the only actual "killing" and "die" search results from Google are people in the described online "Autism Communities" speaking about rhetorical issues of concern regarding killing and dying, not actual people in society discussing these issues with ill intent over disability first language, per Autistic People or Autistics.

It can be an odd, anxious, or expressionless face that brings forth the real hatred from people's hearts, instead of a disability first label of identity on a spectrum. That is not a myth. This is seen in cruel reality in a historical picture of a person's face in the link below, well before there was any hint of offense to come in the future.

This is what some people on the spectrum actually experience in life, that requires no label what so ever. Regardless of what this young man's diagnosed condition might have been, it is a similar anxious expressionless face seen in many young androgynous males who actually have a label on a spectrum.

It is a reality check that the Google Algorithm and the Autistic Label is the last thing some people on the spectrum have to fear. This online "Autism Community" generated algorithm myth is not helping that reality that some young men on the spectrum live with every day.

It is hard to read the over 500 comments, in this link, and it is not suggested for those that are easily triggered by this reality, but it can bring another perspective to this issue.

The second link, from the Wrong Planet website, is refreshing at a look of the power of the minds of people on the spectrum using logic instead of fear to debunk a myth over a Google Auto Complete Search Algorithm that has no soul to determine intent or rhetorical content of internet chatter over disability first labels used in personal preference for identity.

There is nothing to fear of substance from this Algorithm Myth.

However, it does not appear that even people on the spectrum can make the unwarranted fear go away.

http://usnews.nbcnews.com/_news/2013/04/02/17572857-new-photo-of-newtown-shooter-adam-lanza-released-with-college-records?pc=25&sp=0#discussion_nav

http://www.wrongplanet.net/postt225076.html



"Don't Let it Show" by the Alan Parson's Project:




http://www.youtube.com/watch?v=0mY-zdEJkNU


 

Autism, the Internet and "Ideological First Identity", a Collection of Thoughts:

http://katiemiaaghogday.blogspot.com/2013/05/autism-internet-and-ideological-first.html







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Wednesday, April 10, 2013

The Major Factor Underlying the Increase in Rampage Killings


When the Sandy Hook Incident was in the heat of the moment, I attempted to provide information that would describe the complexity of the issue, on the Wrong Planet website, to avert the attention from the one factor that was in focus in the Autism Community.  I provided an informal Poll to analyze many factors potentially associated with the increase of rampage killings in the last 30 years. 

It was an extremely interesting discussion, with a meeting of the minds on the spectrum that is linked at the bottom of this blog entry.  My description of the issue is provided here:

http://www.motherjones.com/politics/2012/07/mass-shootings-map?page=2

From the timeline provided in the link above, it appears that mass murders/spree killings (FBI definition of 4 or more killed other than the shooter) have increased dramatically in the last three decades from 12 to 21 to 29.

What is also interesting is that in the first decade there were only 2 shooters under the age of 30 and 22 in the last 2 decades.

What is perhaps the most alarming trend is that there have been 22 incidents in the last 5 years, almost twice as many in the entire first decade, and one more than the second decade.

All of these rampage killings were accomplished with guns, the majority of which were identified purchased legally. Most of the individuals were identified as having some type of mental disturbance.

http://news.nationalpost.com/2012/12/20/by-2015-firearm-fatalities-will-likely-exceed-traffic-fatalities-in-the-united-states/

While overall violent crime and murder statistics continue to decrease in the US since the early 90's, the low for gun fatalities per homicides, suicides, and accidents was identified in the year 2000, and has been reported slowly increasing in the decade between 2000 and 2010.

Interestingly, there is one survey that suggests the percentage of guns in households has actually decreased since 2004, suggesting there are 70M guns in homes. However, another survey suggests 300M, per registered and unregistered guns.

The overall factors of mental illness/disturbance, legally purchased guns, the use of guns in every crime, and male participation at 98%, are factors that have stayed relatively the same over the three decades in these studied mass murders/spree killings. 


What has changed dramatically is the demographic of the age of males involved and the frequency of the incidences.

What was once a crime almost entirely limited to middle aged males, is now a crime that is approaching 44 percent in the last two decades for males under the age of 30, and 38 percent for males under the age of 26.

In the first decade there were 16 percent under the age of 30, and 0 percent under the age of 26.

If one takes the increase of that under 30, male demographic out of the equation in the last 2 decades, there is not a substantial increase of mass murders/killing sprees, overall, in the last two decades until the last 5 years.

A common psychological element that can be identified across decades in the timeline provided, regardless of identified mental illness/disturbance, age, or target selected to kill, has also stayed relatively the same over three decades of reported rampage killings: a loss or absence of a viable social role for the individuals involved and the killing and violence is directed at some demographic in society.

It appears what was once a type of violent crime almost limited to middle aged disenfranchised males is now becoming more of an issue for younger disenfranchised males.

Violent Video Games have become increasingly popular, available, accessible, and realistic per the virtual experience since the early 90's. Many of which are associated with using guns and other weapons to kill enemies.
 

Never the less, whether as a result of stricter enforcement of laws associated with drug crime or other factors; murders, violent crime, and crime in general, are reported by the United States Department of Justice, to have overall steadily dropped during that same time period.

Even Serial Killings are reported to have dropped by 300 percent in the 2000's decade, back to the levels seen before a 300 percent increase started in the 1970's.

Rampage killings are a glaring exception to these trends, in the US.

It is worth noting that in many of the violent video games the goal is to kill as many enemies as possible with the most powerful weapons available. Other than military actions under the social norm, the only potential of this outside of the social norm, in real life, is rampage killings.

Even if the killer's medical records are released, and Asperger's becomes officially documented in the legal record, he will be the first of 62 individuals officially diagnosed with Asperger's involved in a rampage killing as defined in the timeline, in the last 3 decades in the US, making up 1.6 percent of that assessed demographic.

That is a potential demographic subgroup as rare as the one female identified as participating in a rampage killing over 3 decades. Neither of which could statistically be identified as even a significant factor associated with rampage killings.

http://en.wikipedia.org/wiki/Federal_Assault_Weapons_Ban

In one final and potentially salient note in the future for those that do or don't want to see some of the "assault weapons banned" for sale, the 10 year Federal Assault Weapons Ban expired in 2004 after there was a dramatic increase in the late 90's in Rampage Killings that did decrease substantially in the early 2000's.

The recent use of legally obtained weapons in rampage killings that were under that previous ban that expired in 2004, can certainly not be left out as a significant factor in the total equation of the dramatic increase in rampage killings and number of deaths in those killings over the last five years.

This correlation and the emotional gravity of the Sandyhook rampage killing may eventually be enough to support a new ban for some of those weapons that were banned for sale before.

 

Link to the Wrong Planet Poll, and discussion on this issue:

http://www.wrongplanet.net/postt218916.html


Autism, the Internet and "Ideological First Identity", a Collection of Thoughts:

http://katiemiaaghogday.blogspot.com/2013/05/autism-internet-and-ideological-first.html






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Prevalence of Personality Disorders Co-Morbid with the Autism Spectrum


Personality disorders are linked strongly with Asperger's syndrome in the study linked below, but Anti-Social Personality Disorder, ASPD was not identified at all in the sample of individuals studied with Asperger's Syndrome.  ASPD was only identified in 4 individuals diagnosed with PDDNOS.

The highest association among all groups studied was Obsessive Personality disorder among those diagnosed with Asperger's syndrome at 40%, with the second highest identified as Avoidant Personality disorder among those with Asperger's syndrome at 29%.

All other personality disorders were measured in the 20% range and below in all ASD's studied.

Out of 62 individuals studied with Asperger's syndrome 68% had one personality disorder and 40% had two personality disorders co-morbid with Asperger's syndrome. 40% were reported obsessive, 29% avoidant, 21% schizoid, 19% paranoid, and 16% schizotypal, among others identified in the second link below that provides a table to illustrate the results.

Out of 50 individuals studied with PDD NOS, 60% had one personality disorder and 32% had two personality disorders co-morbid with PDDNOS, with a breakdown of the personality disorders illustrated in the table.

Out of 5 individuals studied with Autistic Disorder 20% had one personality disorder, 0% had two personality disorders; one individual was identified with obsessive personality disorder with no other personality disorders identified in this very small sample of individuals with autistic disorder.

The study is worth checking out as it has some other interesting information.

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2705351/

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2705351/table/T4/

I created a poll on the Wrong Planet website linked below, to see what the opinions of people on the spectrum were associated with this issue.  It was a very interesting discussion.

http://www.wrongplanet.net/postt218441.html


Autism, the Internet and "Ideological First Identity", a Collection of Thoughts:

http://katiemiaaghogday.blogspot.com/2013/05/autism-internet-and-ideological-first.html







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ToM Theory of Mind/"Mind Blindness" and Autism


ToM Theory of Mind/”Mind Blindness” is much more complex than reading non-verbal expression, however it is described as a spectrum of abilities/challenges, where the described difficulties can be much different in individuals across the Autism Spectrum.

The described abilities/challenges are also associated with ADHD and Schizophrenia.

Interestingly, perhaps ironically, a developmental milestone missed - the common tendency for small children to "lie" to avoid punishment, is a sign there could be a "difficulty".

It is also associated with blunt descriptive assessments of other people that do not assess potential "feelings". I will never forget an Asperger’s support group meeting where a "little professor" asked the female speaker right in the middle of his monologue, "lady why are you wearing so much make up". His assessment was correct. :)  But....

I still have to catch myself from doing things like that, that are not as obviously offensive. :)

Also interesting, in the ability to sense the pain of others, studies show that people diagnosed with Asperger's syndrome are more sensitive to a personal distress of seeing others in physical and/or emotional pain, as a type of emotional contagion. This is described as a heightened instinctual ability though, rather than what is described as ToM/Mind Blindness or what some describe as Cognitive Empathy.


Excellent descriptions by Wiki linked below.

Theory of Mind:

http://en.wikipedia.org/wiki/Theory_of_mind


Cognitive vs. Affective Empathy:

http://en.wikipedia.org/wiki/Empathy#Cognitive_versus_affective_empathy

Personal Distress:

 
http://en.wikipedia.org/wiki/Personal_distress


Autism, the Internet and "Ideological First Identity", a Collection of Thoughts:

http://katiemiaaghogday.blogspot.com/2013/05/autism-internet-and-ideological-first.html






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Sunday, April 07, 2013

Parents and "Privilege" on the Autism Spectrum


Part of the reason, I would not disrespect a person identifying as a parent of another individual on the spectrum, is that I have been in all three places.

I still love and respect my parents, even though one of them was emotionally distant and close to that imaginary border of a broader autism phenotype.
 

As far as I can see, if I did not, I would be guilty of lacking empathy for those very much like me. However, my moral code belongs to me, and only me. 

There is an element of “overall parent hating” that also includes all of what is described as "neurotypical", and "Parent run" Autism Advocacy Organizations. I have observed some participating in this element of effort that I personally do not agree with.

However, it is clear to me, in the personal stories I have heard, particularly in the female dominated and described "neurodiversity community" that the parent-child relationship was not the same unconditional love I received from at least one of my parents, for some other people.

I also find myself attempting to share empathy for that perspective that I cannot possibly fully share.

I can remember one autism online community that has a history of being militant against "parents of people on the spectrum", and there was one individual that tried to get a message across to others, in his signature line that stated - "life looks different past forty, my parents are dead".

That puts the issue in a perspective of a general level of respect for parents, for the love and compassion that often comes with raising a child on the spectrum that not everyone can fully relate to.
 

However, some people on the spectrum find themselves fully depending on their parents through a substantial course of their lifetime, and fully appreciating that. I am among those individuals that share that ideology, even though I found a way to support myself.

I have my parents to thank for that.  
                  
 


                                                         

                                                      



I also see my distinct privilege on the spectrum in finding a way to support myself. I fell into an employment niche that worked for me, was able to find a spouse that complemented my various challenges in making me stronger, buy a house, and the things that many people only dream of in life, on or off the spectrum.

I lived at home until I was 28 and lived with my sister until 29. If it were not for that support, I would have been dead and/or institutionalized many years before that.

My mother raised us alone and lived a struggle from one paycheck to the next. However, one thing we never lost for many years was hope.

I fully recognize my privilege in many areas of life. I did not fully appreciate the efforts of my mother until I had a child of my own who was challenged more than I was in my life. I could not fully imagine it until then. However, if I did not have a child, I am not sure I ever would have.
 

I have no problem admitting there is a level of selfishness that can come with Autism, but it took me decades in fully realizing that, to admit it. I had little to no clue what selfish even meant.
 

It was hard for me to separate the rest of the world from me, but I was born that way, what can I say. That is what the word Autistic has meant for over a century, well before there was a diagnosis for the condition.

I see myself in that younger person in some avenues of online autistic communication. It is part of why I provide much different perspectives, in hopes that some others might not have to wait for decades for that kind of awareness that is not an inherent one for some.

However, the one thing I have experienced that I cannot do without is hope for a next moment. Something I currently have, at least for this moment, that I feel privilege for more than anything else in life. 


 

Autism, the Internet and "Ideological First Identity", a Collection of Thoughts:

http://katiemiaaghogday.blogspot.com/2013/05/autism-internet-and-ideological-first.html






"AutisticS Peeks!"


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AS
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Autistic Spectrum
Perception

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Perspective