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justdrew wrote:debating a cause for a nebulous ill-defined "syndrome" supposedly occurring along a "spectrum" who's ends don't even look similar and that we have no idea what "it" even "is" is pointless and foolish. You all accept that there is a thing called "autism" that some (children) "have" - I'm saying this is a socially constructed non-disease. There is no disease model for the autism spectrum. At one end there are persons who clearly suffer from cognitive impairment and developmental delays who display a loose set of typical behaviors. These persons I feel would be fair to refer to as autistic, if we wanted to keep the term at all, which I think is counterproductive actually. The other end of the hypothesized "spectrum" is very loosely defined.
http://en.wikipedia.org/wiki/Autism_spectrum
the entirely hypothetical http://en.wikipedia.org/wiki/Asperger_syndrome
and these pro's are now working up whole new checklists to put people into diagnostic buckets with...
see for example... Pathological Demand Avoidance. Read those diagnostic criteria.
look here http://en.wikipedia.org/wiki/Classical_autism under "causes"... They are describing how complex the genetic basis must be. There is no genetic basis any more than there is a genetic basis for being a selfish un-curious conformist shithead. The complexity is so high, because they are looking at basic human mental variability. The DISEASE exists ONLY in the Parents and the Society that refuse to accept that not all people are the same. Accommodate the child's needs and there will be no problem in the long run. Insist that every square peg be hammered into the round holes and we've got a recipe for neuro-atypical holocaust.
Autism has been here all along.
Considered as an evolutionary condition with far-reaching social implications, its full presence and impact remain hidden in plain sight, unrecognized and uncredited.
Part neurological mystery, part social construct, and part secret society unbeknownst even to its own members, autism does not lend itself to explanation by those who hold it apart from society, from themselves, or from consciousness itself. Definitions are revised, overhauled, and abandoned all while efforts to explore and examine this condition on its own terms are only now gaining momentum.
Shift Journal aims to showcase and encourage such efforts. Entertaining the notion of autistic as a legitimate way to be in the world, from the crossroads of theory, society, and personal experience, Shift welcomes relevant contributions from all comers.
Mark Stairwalt
Editor and Publisher
Autism as Evolutionary Condition
January 21st, 2010
If the results from these three studies are combined, the overall proportion of left-handers is 13.3 per cent for autistic children and 8.3 per cent for matched controls, not a significant difference. However, if left- and mixed-handers are summed, then the frequency of non-right-handedness among autistic children is considerably higher than that found in age-matched normally developing children, although it is similar to that found in other children of the same intellectual ability (Bishop, D. V. M. (1990). Handedness and developmental disorder. London: Mac Keith Press. p. 111)
There is a close associated between handedness and maturational delay. There is a close association between autism and handedness. There is a close association between maturational delay and autism. There is a close association between a mother’s testosteone levels and her children’s handedness and autism.
Seems pretty clear that a mother’s testosterone levels are closely associated with maturation rate. There is a whole science devoted to maturation rates as those rates relate to evolution. That science is called heterochrony. Consider that autism is an evolutionary condition.
Thirteen Things
You'll Find Here
1. A feminine theory of evolution with estrogen controlling the timing of events.
2. A theory of autism that also explains the origin and evolution of normal human split consciousness (theory of mind).
3. Art and play are elevated to become central to evolution.
4. An integration of Darwin's 3 theories: natural selection, sexual selection & pangensis
5. Biological evolution and social change are joined and reframed as part of an identical process.
6. Teleology, a large scale social trend, is described as a social structure concept.
7. The environment and social structure are elevated to become central to evolution and social transformation.
8. Human migration patterns emerge as influential in cerebral development.
9. Mating two humans with only very distant ancestors (50,000 year gaps) can create autism and/or forms of hybrid vigor.
10. Evolution evolves. This site describes how the actual structures of evolution have transformed.
11. Female infanticide is redefined as a powerful stabilizing force in patrifocal social structure.
12. A century of dropping puberty onset is reducing cerebral synapses & diminishing spiritual experience.
13. Understanding autism we discover the etiologies of a number of currently mysterious diseases and conditions.
What this boils down to is this. The Orchestral Theory of Evolution is the study of the rates and timing of maturation with testosterone levels impacting rate and estrogen levels controlling timing, with those environmental or social structure adjustments that influence levels of testosterone and estrogen determining the speed, timing, features and direction of evolution
For years Andrew Wakefield has been vilified and persecuted for publishing an article in Lancet on February 28, 1998.
Since then, he has been accused of inventing a gastro-intestinal illness and endangering the world because he reported that some of the 12 parents in that UK study had stated that their children’s autistic and gastro-intestinal symptoms had started soon after they had received an MMR vaccination.
It is safe to propose that prior to 1998, parents (and pediatricians) in Utah, Minnesota. North Carolina and elsewhere in the United States had not heard of Dr. Wakefield and had no idea that autistic regression sometimes followed MMR vaccination.
I have been interested in VAERS, the Vaccine Adverse Event Reporting System since it was launched and have acquired some expertise in understanding and evaluating individual reports.
It was with some surprise that I recently discovered that there had been 15 reports filed with VAERS prior to December 31, 1997 by parents stating that their children had developed autistic symptoms after receiving MMR vaccines in the United States.
There seems to be general agreement about the following two statements:
1: A report to VAERS does not necessarily imply causation
2. Only a small percentage of vaccine adverse events are ever reported to VAERS
...
• From 1970 to 1993, forty eight (48) children met the inclusion criteria of an acute encephalopathy 2 to 15 days after receiving measles vaccine, alone or in combination (MR or MMR)
• Eight children died and “the remainder had mental regression and retardation, chronic seizures, motor and sensory deficits, and movement disorders” (permanent brain impairment)
• The patients ranged in age from 10 months to 49 months, with a median age of 15 months and a mean age of 17.5 months.
• The onset of neurologic signs or symptoms occurred with a nonrandom, statistically significant distribution on days 8 and 9 following vaccination.
The authors concluded that “This clustering suggests that a causal relationship between measles vaccine and encephalopathy may exist as a rare complication of measles immunization.”
~~~~~~~~
Conclusions
On February 28, 1998, thirteen years ago today, Dr. Andrew Wakefield and others published an article in Lancet.
Although Dr. Wakefield never once said that MMR vaccination caused autism, his life has been ruined and his license to practice medicine has been revoked because he dared suggest that research was needed to look at all the possible causes of autistic regression.
It is now clear that before they ever heard of Dr. Wakefield, some US parents had also suspected that their children’s autism and encephalopathy were at least chronologically related to their MMR vaccination.
Fourteen of those parents reported their children’s reactions to the Vaccine Adverse Event Reporting system between May 28, 1992 and October 4, 1997.
Others filed petitions with the National Vaccine Injury Compensation Program.
It is time to stop attacking the messenger.
It is also time to honestly investigate all the possible causes, without exception, of the terrible calamity that has decimated a generation.
F. Edward Yazbak MD
Falmouth, Massachusetts 02540
February 28, 2011
For years Andrew Wakefield has been vilified and persecuted for publishing an article in Lancet on February 28, 1998.
Since then, he has been accused of inventing a gastro-intestinal illness and endangering the world because he reported that some of the 12 parents in that UK study had stated that their children’s autistic and gastro-intestinal symptoms had started soon after they had received an MMR vaccination.
It is safe to propose that prior to 1998, parents (and pediatricians) in Utah, Minnesota. North Carolina and elsewhere in the United States had not heard of Dr. Wakefield and had no idea that autistic regression sometimes followed MMR vaccination.
I have been interested in VAERS, the Vaccine Adverse Event Reporting System since it was launched and have acquired some expertise in understanding and evaluating individual reports.
It was with some surprise that I recently discovered that there had been 15 reports filed with VAERS prior to December 31, 1997 by parents stating that their children had developed autistic symptoms after receiving MMR vaccines in the United States.
There seems to be general agreement about the following two statements:
1: A report to VAERS does not necessarily imply causation
2. Only a small percentage of vaccine adverse events are ever reported to VAERS
• From 1970 to 1993, forty eight (48) children met the inclusion criteria of an acute encephalopathy 2 to 15 days after receiving measles vaccine, alone or in combination (MR or MMR)
• Eight children died and “the remainder had mental regression and retardation, chronic seizures, motor and sensory deficits, and movement disorders” (permanent brain impairment)
• The patients ranged in age from 10 months to 49 months, with a median age of 15 months and a mean age of 17.5 months.
• The onset of neurologic signs or symptoms occurred with a nonrandom, statistically significant distribution on days 8 and 9 following vaccination.
The authors concluded that “This clustering suggests that a causal relationship between measles vaccine and encephalopathy may exist as a rare complication of measles immunization.”
It is also time to honestly investigate all the possible causes, without exception, of the terrible calamity that has decimated a generation.
Japan halts Pfizer, Sanofi vaccines after four die
Reuters
By James Topham James Topham – Mon Mar 7, 4:16 am ET
TOKYO (Reuters) – Japan's health ministry has halted the use of vaccines made by Pfizer Inc and Sanofi-Aventis SA to prevent meningitis and pneumonia following the deaths of four children.
The infants died shortly after receiving the vaccines and while it was unclear if there was link between the deaths and vaccines, use of Pfizer's Prevenar and Sanofi's ActHIB will be suspended while the deaths are investigated, the ministry said in a statement.
A ministry safety panel is scheduled to discuss findings in the investigations on Tuesday.
In February last year health authorities in the Netherlands said no relation was found between Prevenar and the deaths of three infants who had received the vaccine.
Three of the children that died in Japan were administered Prevenar together with ActHIB. In addition, three of the children also received a mixed vaccine against diphtheria, whooping cough and tetanus on the same day they received the other vaccines.
Three of the four children died a day after being immunized. The deaths happened between March 2 and March 4.
Representatives for Pfizer and Sanofi in Tokyo said the companies were cooperating with the investigation.
A spokesman for Sanofi said that the company has shipped more than 3 million doses of ActHIB in Japan since 2008 while a spokesman for Pfizer said the firm has distributed more than 2 million doses of Prevenar in Japan since last year.
justdrew wrote:debating a cause for a nebulous ill-defined "syndrome" supposedly occurring along a "spectrum" who's ends don't even look similar and that we have no idea what "it" even "is" is pointless and foolish. You all accept that there is a thing called "autism" that some (children) "have" - I'm saying this is a socially constructed non-disease. There is no disease model for the autism spectrum. At one end there are persons who clearly suffer from cognitive impairment and developmental delays who display a loose set of typical behaviors. These persons I feel would be fair to refer to as autistic, if we wanted to keep the term at all, which I think is counterproductive actually. The other end of the hypothesized "spectrum" is very loosely defined.
http://en.wikipedia.org/wiki/Autism_spectrum
the entirely hypothetical http://en.wikipedia.org/wiki/Asperger_syndrome
and these pro's are now working up whole new checklists to put people into diagnostic buckets with...
see for example... Pathological Demand Avoidance. Read those diagnostic criteria.
look here http://en.wikipedia.org/wiki/Classical_autism under "causes"... They are describing how complex the genetic basis must be. There is no genetic basis any more than there is a genetic basis for being a selfish un-curious conformist shithead. The complexity is so high, because they are looking at basic human mental variability. The DISEASE exists ONLY in the Parents and the Society that refuse to accept that not all people are the same. Accommodate the child's needs and there will be no problem in the long run. Insist that every square peg be hammered into the round holes and we've got a recipe for neuro-atypical holocaust.
justdrew wrote:look here http://en.wikipedia.org/wiki/Classical_autism under "causes"... They are describing how complex the genetic basis must be. There is no genetic basis any more than there is a genetic basis for being a selfish un-curious conformist shithead. The complexity is so high, because they are looking at basic human mental variability. The DISEASE exists ONLY in the Parents and the Society that refuse to accept that not all people are the same. Accommodate the child's needs and there will be no problem in the long run. Insist that every square peg be hammered into the round holes and we've got a recipe for neuro-atypical holocaust.
CDC To Study Vaccines and Autism
The Centers for Disease Control and Prevention wants to study autism as a possible clinical outcome of immunization, as part of its newly adopted 5-year research agenda for vaccine safety, the agency said on its website.
The CDC will also study mitochondrial dysfunction and the potential risk for post-vaccine "neurological deterioration," and convene an expert panel on the feasibility of studying health outcomes such as autism among vaccinated and unvaccinated children.
The CDC plan adopts recommendations approved by the National Vaccine Advisory Committee of the US Department of Health and Human Services. It also comes one month after the federal government's leading autism body, the Interagency Autism Coordinating Committee (IACC), signaled a shift in research priorities toward environmental triggers for autism, which the IACC said could include toxins, biological agents and "adverse events following immunization."
The Centers for Disease Control and Prevention's Immunization Safety Office Scientific Agenda indentified the need to research "Neurodevelopmental disorders, including autism spectrum disorder (ASD)" as a possible clinical outcome of vaccination.
The plan also seeks to deternine if the mercury-based preservative thimerosal is associated with increased risk for "clinically important tics or Tourette syndrome." The CDC cited one study (Thompson, NEJM, 2007), which "found that increasing exposure to mercury from birth to age 7 months was associated with motor and phonic tics in boys," and added that "an association between exposure to thimerosal and tics was found in two earlier studies (Andrews, Pediatrics, 2004; Verstraeten, Pediatrics, 2003)."
And, noting that the IACC federal autism panel "suggested several studies including vaccinated versus unvaccinated children to determine if there are differences in health outcomes," the CDC said it will convene an "external expert committee to offer guidance on the feasibility of conducting such studies and additional studies related to the immunization schedule, including studies that may indicate if multiple vaccinations increase risk for immune system disorders."
Meanwhile, the IACC has signaled a shift in research priorities into the causes of autism, moving away from genetic studies in favor of investigating the interaction between genes and environmental factors, which it said could include toxins, biological agents and vaccines.
The IACC, among other things, helps direct millions of federal dollars into autism research. Until now, the IACC's updated strategic plan noted, "the majority of this funding (was) directed toward the identification of genetic risk factors (with) less funding and attention toward environmental research."
A number of environmental factors are now being researched, the IACC said, adding that, "Recent studies suggest that factors such as parental age and exposure to infections, toxins, and other biological agents may confer environmental risk. These findings require further investigation."
As for vaccines, "Numerous epidemiological studies have found no relationship between ASD and vaccines containing the mercury based preservative thimerosal," the IACC noted. "These data, as well as subsequent research, indicate that the link between autism and vaccines is unsupported by the epidemiological research literature. However, the Institute of Medicine report acknowledged that the existing population-based studies were limited in their ability to detect small susceptible subpopulations that could be more genetically vulnerable to environmental exposures."
http://www.huffingtonpost.com/david-kir ... 37360.html
University of Pennsylvania's Dr. Brian Strom, who has served on Institute of Medicine panels advising the government on vaccine safety says the prevailing medical opinion is that vaccines are scientifically linked to encephalopathy (brain damage), but not scientifically linked to autism.
Dr. Strom said he was unaware that human DNA was contained in vaccines but told us, "It does not matter...Even if human DNA were then found in vaccines, it does not mean that they cause autism."
Why could human DNA potentially cause brain damage? The way Ratajczak explained it to me: "Because it's human DNA and recipients are humans, there's homologous recombinaltion tiniker. That DNA is incorporated into the host DNA. Now it's changed, altered self and body kills it. Where is this most expressed? The neurons of the brain. Now you have body killing the brain cells and it's an ongoing inflammation. It doesn't stop, it continues through the life of that individual."
...in all the major social sheparding arguments of today.
sorry to go off on a tangent sounder. yeah, the first response is to laugh...
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