From Hell To Veins

May 5, 2012

More Damage Control For Pro Vaccine. Vaccine Test Monkeys Develop Autism.

Editor’s Note:
Well, one thing’s for sure, this latest vaccine bombshell should keep big pharma’s skeptic lackeys employed ‘doctoring up’ more disinfo to keep you from seeing what’s behind the medical mafia curtain.
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Cover Up Continues: Monkeys Injected With Vaccines Develop Autism
http://blog.alexanderhiggins.com/2012/05/05/cover-continues-monkeys-injected-vaccines-develop-autism-129611/

Scientists find monkeys develop autism-like reactions injected with vaccines given to children including Measles-Mumps-Rubella (MMR) and several Thimerosal mercury-containing vaccines.

Scientists are making incredible break-troughs in some fields of research. Take for example the field of nano-technology in which scientists have been able to use just two molecules to create the world’s smallest radio radio station which communicates using just photons. Or the field of neuroscience in which scientists have been able to connect microchips to the brains of rats that allow them to upload and download memories and even transfer learned behaviors from one rat to another. Or even microscopic nano-rockets that travel through the blood stream inside of the human body.

As amazing as these technologies are it is striking that other fields of research have been frozen in time. It is perplexing, to say the least, that 43% of the US population will develop cancer and 22% percent will die of cancer while scientists and government agencies downplay the risks of radiation in everything from milk to drinking water.

Just as amazing is the surge of autism in the United States, with the latest CDC data (from 2008!) showing that 1 in 88 children now suffer from autism while studies emerge linking high fructose corn syrup in processed industrial foods as well as mercury in vaccines and dental fillings to the disease

While the rate of autism continues to skyrocket studies and scientific information continue to be dismissed as conspiratorial fear-mongering as federal regulators are at a loss for providing explanations for the skyrocketing outbreak.

Instead they refuse to ban the use of BPA in our foods or even to refuse to allow the public to know they are eating GMO foods that has been genetically modified to produce toxic pesticides that are killing humans and bees.

Now the latest scientific research out of the University of Pittsburg shows once again that monkeys develop autism symptoms when given vaccines that the government forces children to take, such as Measles-Mumps-Rubella (MMR) and several very common Thimerosal mercury-containing vaccines which include flu shots,

Vac Truth reports:

Monkeys Get Autism-like Reactions to MMR & Other Vaccines In University of Pittsburgh Vaccine Study

A University of Pittsburgh study showed vaccines altered the behavior in monkeys.

Someone did perform safety studies the U.S. Centers for Disease Control and Prevention (CDC) and the U.S. Food and Drug Administration (FDA) should have mandated be performed and vetted BEFORE numerous vaccines were released into the public sector for mass vaccinations.

Lead investigator Laura Hewitson, PhD, probably dropped a bombshell when she and her colleagues completed a macaque monkey (primates) study of the very same vaccines given to children during 1994-1999, i.e., the Measles-Mumps-Rubella (MMR) vaccine and several Thimerosal mercury-containing vaccines injected into children during that time frame when the autism spectrum disorder skyrocketed.

The results of that pilot study were published as a Research Paper in Acta Neurobiological Experimentals in 2010 and titled “Influence of pediatric vaccines on amydgala growth and opioid ligand binding in rhesus macaque infants: A pilot study.” [1] Even though there was alleged controversy revolving around Hewitson’s monkey studies, e.g., charges of conflicts of interest since she filed a claim with the vaccine court on behalf of her child, [2] the information generated needs to be revisited and duplicate studies need to be undertaken. Why haven’t they? Is there too much influence from vaccine makers not to do them? Parents need to make demands on the U.S. Congress to require such safety studies on monkeys be duplicated immediately, plus suspend all mandates on vaccinations until the study results are in. Did Dr Hewitson become another professional persona non-grata because she may have been on the right track?

Congress needs to consider seriously the Hewitson, et al. report that stated:

“Vaccine-exposed and saline-injected control infants [monkeys] underwent MRI and PET imaging at approximately 4 and 6 months of age, representing two specific timeframes within the vaccination schedule. …

“These results suggest that maturational changes in amygdala volume and the binding capacity of [11C]DPN in the amygdala was significantly altered in infant macaques receiving the vaccine schedule.” [1]

That alone should be the explicit reason for duplicating the monkey study with independent non-pharmaceutical industry conflict of interest scientists.

In this author’s opinion, no one has bigger conflicts of interest in study outcomes than the pharmaceutical makers who routinely perform them. Those are the very studies that should be subject to the same criticism as Dr Hewitson’s. Why aren’t they? Good question?

For those keeping track data, ASD went from 1 in 5,000 in the 1990s to the recently acknowledged [March 2012] figures of 1 in 88 along with 1 in 6 children in the USA having developmental disabilities. These stats were generated for data in the years 2006 to 2008. [3] There’s a 4 to 6 year lag time. Could ASD be 1 in 50 by now at the rate it is escalating?, especially since there’s a heavier push on mandates for vaccinations.

According to the Hewitson, et al. research study, biological changes and altered behaviors did occur in vaccinated monkeys, which resembled and were similar to those observed in ASD diagnosed children. However, there were no such symptoms showing or present in unvaccinated monkeys. Don’t you just gotta love those little monkeys! Guess what else the ASD monkeys came up with, and Dr Wakefield is gonna like this one: Gastrointestinal problems manifested in vaccinated macaques such as “many significant differences in the GI tissue gene expression profiles between vaccinated and unvaccinated animals.” [3] It’s been a deeply debated topic within medicine that vaccinated children who contract ASD also have GI tract issues. Personally, I gotta wonder how the British Medical Journal is going to deal with encrusted dried egg on its face when duplicate studies confirm the Hewitson monkey results. Perhaps the infamous BMJ retraction of the Wakefield article and Doctor’s professional evisceration, commonly referred to as the “Wakefield Syndrome,” euphemistically speaking is medicine protecting its vested interests.

Those little monkeys, however, came up with some other significant information that led former National Institutes of Health director Dr Bernadine Healy to voice some bon mots like:

“I think public health officials have been too quick to dismiss the hypothesis as ‘irrational,’ without sufficient studies of causation…without studying the population that got sick.”

“I have not seen major studies that focus on 300 kids who got autistic symptoms within a period of a few weeks of the vaccines.” [4]

Perhaps the most on-point quote regarding the monkey study came from Scott Bono, the National Autism Association chairman, i.e., something those who are accused of being against vaccinations have been questioning and demanding:

“To date, the CDC has conducted no safety testing on the possible harmful effects of simultaneously administering multiple vaccines to infants, and has steadfastly refused to state a preference for mercury-free vaccines to be given to children and pregnant women. It’s time for HHS and Congress to step in and take vaccine safety away from the CDC.” [4]

This author’s retort to Mr. Bono’s remark is that vaccine safety should be taken away from the Food and Drug Administration too! I’d like to remind readers that Congress is more at fault than anyone in this vaccine debacle. Congress has oversight and it has dropped the ball big time, probably due to all the lobbyists from Big Pharma who prowl the halls of Congress with deep pockets and nice expensive luncheon dates.

One of the issues I feel Congress has been remiss about is that it has not demanded safety studies and interaction of multiple vaccines studies BEFORE being placed into the marketplace. According to common and accepted knowledge, no such safety research or studies have been done on the current childhood vaccination regimen, except until the Hewitson ‘monkey business’ that was funded by independent, private money, for which everyone, I think, should be eternally grateful. However, the study had to be shot down since it was not favorable to vaccine makers. Why isn’t someone else duplicating the monkey studies? Are they afraid of becoming another victim of science? Why, when isn’t that what medical science should be all about: investigating problems and theories, publishing results, and interacting with other sciences, NOT excommunication as if they were breaking some religious dogma. Or, do they, in some vested interests minds?
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For sake of the future of our nation and our children it is time for the public to stand up against this tyranny and demand that proper research be conducted outside of the influence of corporations, special interest groups, and lobbyists before this epidemic destroy the entire population.

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July 26, 2010

The Autism Epidemic. Conflicts, Collusion And Much Sourced Documentation.

The following was emailed to me by ‘Vaccine Liberation’.

I just want to say mercury poison is NOT the only thing that can give rise to autistic (and other) symptoms.
Aluminum. formaldehyde, fluoride can even wreck more havoc on the nervous system, brain and organs.

Also, it has been proven and WELL KNOWN in the field of toxicology that mercury poisoning can occur on the ‘NANO-particulate’ level.

If I have NOT hyperlinked ANY of the links OR you find ANY that do not work please comment so. I’ll do what I can to correct the problem.
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Autism Epidemic, First Do No Harm, Conflicts and Collusion, and the Precautionary Principle

Philip Rudnick 6 July 2010

I. The Autism Epidemic

Autism was completely unknown in the United States before 1943. The incidence of autism
in the 1960’s was 1/10,000.
Treffet, Darold
Epidemiology of infantile autism
Archives of general psychiatry1970, (5) 431-38

An autism surge began in the period 1980-1988.
HYPERLINK “http://www.ourstolenfuture.org/NewScience/behavior/2002/2002-10byrd.htmhttp://www.ourstolenfuture.org/NewScience/behavior/2002/2002-10byrd.htm

McDonald ME, Paul JF.
Environ Sci Technol. 2010 Mar 15;44(6):2112-8.
National Health and Environmental Effects Research Laboratory, U.S. Environmental Protection Agency, MD-B343-06, Research Triangle Park, North Carolina 27711.

Twenty-two years later (2010) there are 730,000 youths diagnosed with autism.
Time Magazine, March 8, 2010, p.44.
From another source:
Based on statistics provided by the Autism Society of America, it is estimated that approximately 1 million youth in this country have autism, which does not include Pervasive Developmental Disorders (PDD), Asperger’s and other spectrum disorders. A new case of autism is diagnosed nearly every 20 minutes or approximately 24,000 new cases per year.
HYPERLINK “http://www.symptoms-of-autism.com/autism/temple-grandin-focus-on-autism-and-aspergers-syndrome.html” http://www.symptoms-of-autism.com/autism/temple-grandin-focus-on-autism-and-aspergers-syndrome.html

The current autism incidence is 1/91, a 110-fold increase since the 1/10,000 figure of the 1960’s.
HYPERLINK “http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-1522v1http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-1522v1

Based on statistics from the U.S. Department of Education and other governmental agencies, autism is growing at a rate of 10-17 percent per year. At this rate, the Autism Society estimates that the prevalence of autism could reach 4 million Americans in the next decade.
HYPERLINK “http://www.autism-society.org/site/PageServer?pagename=about_whatis” http://www.autism-society.org/site/PageServer?pagename=about_whatis

The autism epidemic is not an impossible 110-fold “genetic-increase” epidemic,
nor a 110-fold “better-or-shifting-diagnosis increase” epidemic.

HYPERLINK “http://www.environmentalhealthnews.org/ehs/news/autism-and-environmenthttp://www.environmentalhealthnews.org/ehs/news/autism-and-environment

“Recent increases in chronic diseases like diabetes, childhood asthma, obesity or autism cannot be due to major shifts in the human gene pool as those changes take much more time to occur. They must be due to changes in the environment, including diet and physical activity, which may produce disease in genetically predisposed persons.”
Francis S. Collins, M.D., Ph.D., Evidence to US House of Representatives Committee May 2006

Thomas Insel’s admission about autism at MIT, 2 Dec 2009
“I don’t know of any data quite like this over a 20 year period which shows this striking increase.” Insel said we don’t know what’s driving this. We know it’s not because of people who were labeled something else. He said it’s not diagnostic substitution.
HYPERLINK “http://mitworld.mit.edu/video/756″ http://mitworld.mit.edu/video/756
HYPERLINK “http://www.ageofautism.com/2010/06/iacc-head-dr-tom-insel-talks-about-autism-at-mitdec-2009.html” http://www.ageofautism.com/2010/06/iacc-head-dr-tom-insel-talks-about-autism-at-mitdec-2009.html

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II. First Do No Harm – Ignoring the Evidence of Harm of Thimerosal in Vaccines

In 1929, K.C. Smithburn, a Eli-Lilly-sponsored physician, intravenously injected thimerosal
into 22 patients terminally ill with Meningococcal Meningitis. No rashes or site reactions were observed. All the patients died shortly afterwards. In January 1931, the American Journal of Hygiene published a paper submitted by H.M. Powell and W.A. Jamieson citing the Smithburn study.
Powell HM, Jamieson WA. Merthiolate as a Germicide. Am J Hyg 1931;13:296-310.
They claimed that this study showed that injected thimerosal was safe. This study was the basis of the FDA’s approval of thimerosal in vaccines. The FDA today still refers to the 1931 Powell and Jameison study on its Web site as indication of the “safety and effectiveness” of thimerosal as a preservative.
HYPERLINK “http://www.fda.gov/cber/vaccine/thimerosal.htm#tochttp://www.fda.gov/cber/vaccine/thimerosal.htm#toc
“7 of 22 subjects were observed for only one day, the specific clinical assessments were not described, and no laboratory studies were reported.”

From 1931 until 1991, thimerosal was legally added to all pediatric vaccines as a preservative.
These vaccines continued to be used until their stocks were exhausted. Thimerosal continues
to be added to injectable flu vaccines recommended by the CDC and AAP for administration to
children and pregnant women on a routine yearly basis.

1. All forms of mercury are extremely neurotoxic, particularly organomercuric compounds,
and particularly when injected.

2. As with all toxic compounds, the toxicity of mercury is inversely related to body weight,
and is therefore particularly acute for fetuses, infants and children.

3. The toxicity of mercury is also particularly acute for fetuses, infants and children
as they do not yet have fully developed nervous systems.
HYPERLINK “http://articles.mercola.com/sites/articles/pages/the-danger-of-excessive-vaccination-during-brain-development.aspxhttp://articles.mercola.com/sites/articles/pages/the-danger-of-excessive-vaccination-during-brain-development.aspx (172 references)

4. NO preservative, including thimerosal, is necessary in single-dose vials.

The principle of “First Do No Harm” dictates that if two necessary medical courses of action of comparable efficacy exist, you must choose the one that is less harmful or less potentially harmful. For flu vaccines administered to children and pregnant women, one would think that this would simply mandate the use of single-dose, thimerosal-free vials exclusively for this population. The Vaccine Establishment, however, has rejected this proposal on the non-medical grounds of being too inconvenient and too expensive, and on the medical grounds that they know with absolute certainty that thimerosal in vaccines administered to all children and all pregnant women/fetuses cannot possibly cause any harm.
“Is it safe for children to receive an influenza vaccine that contains thimerosal? Yes… Is it safe for pregnant women to receive an influenza vaccine that contains thimerosal? Yes…”
HYPERLINK “http://www.cdc.gov/FLU/ABOUT/QA/thimerosal.htmhttp://www.cdc.gov/FLU/ABOUT/QA/thimerosal.htm
Their proof – conflicted and compromised studies, such as the CDC-funded Thorsen/SSI, Simpson/CDC, Danish vaccine studies:
HYPERLINK “http://www.ageofautism.com/2010/03/first-fraud-dr-poul-thorsen-and-the-original-danish-study.html” http://www.ageofautism.com/2010/03/first-fraud-dr-poul-thorsen-and-the-original-danish-study.html
and the CDC-funded Italian vaccine study:
HYPERLINK “http://childhealthsafety.wordpress.com/2009/01/28/cdc-fraud-tax-dollars-and-italian-vaccine-mercury-study/http://childhealthsafety.wordpress.com/2009/01/28/cdc-fraud-tax-dollars-and-italian-vaccine-mercury-study/

HYPERLINK “http://www.lakelandtimes.com/main.asp?SectionID=10&SubSectionID=10&ArticleID=11369http://www.lakelandtimes.com/main.asp?SectionID=10&SubSectionID=10&ArticleID=11369

Thimerosal is good for you – Garbage In – Garbage Out
HYPERLINK “http://www.ageofautism.com/2010/03/autism-vaccines-thimerosal-further-study-needed.htmlhttp://www.ageofautism.com/2010/03/autism-vaccines-thimerosal-further-study-needed.html

At the same time, the Vaccine Establishment denigrates and dismisses, without exception,
the voluminous evidence of harm from injected mercury.
HYPERLINK “http://www.icmr.nic.in/ijmr/2008/october/1004.pdfhttp://www.icmr.nic.in/ijmr/2008/october/1004.pdf
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III. Conflicts of Interest and Collusion of the Vaccine Establishment

Vaccine Establishment Conflicts of Interest – Some Examples:

CDC places conflicted scientists on the Advisory Committee on Immunization Practices (ACIP)
Vaccine Recommendations by Conflicted CDC Committee Members:
HYPERLINK “http://www.laleva.org/eng/2004/03/vaccinations_risks_and_myth_upi_investigates_the_vaccine_conflict_and_cdc_corruption.htmlhttp://www.laleva.org/eng/2004/03/vaccinations_risks_and_myth_upi_investigates_the_vaccine_conflict_and_cdc_corruption.html

HYPERLINK “http://www.ageofautism.com/2009/08/when-vaccine-development-is-family-business-thomas-insels-conflicted-role-on-vaccines-and-autism.htmlhttp://www.ageofautism.com/2009/08/when-vaccine-development-is-family-business-thomas-insels-conflicted-role-on-vaccines-and-autism.html

HYPERLINK “http://www.gaia-health.com/articles101/000137-merck-hires-gerberding-cdc.shtml http://www.gaia-health.com/articles101/000137-merck-hires-gerberding-cdc.shtml

HHS-Gardasil
HYPERLINK “http://www.ageofautism.com/2010/05/a-license-to-kill-part-3-after-gardasils-launch-more-victims-more-bad-safety-analysis-and-a-revolvin.htmlhttp://www.ageofautism.com/2010/05/a-license-to-kill-part-3-after-gardasils-launch-more-victims-more-bad-safety-analysis-and-a-revolvin.html

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Vaccine Establishment Collusion – Some Examples:

Simpsonwood Conference and the Problem of a Thimerosal-Autism Link

By 1999, the CDC knew from its own evidence that there was a thimerosal link to autism. That’s when CDC researcher Tom Verstraeten found it. Here’s how he reported it in a Dec. 17, 1999, email to his colleagues, Robert Davis and Frank Destefano. The subject line was, “It just won’t go away…”
HYPERLINK “http://www.lakelandtimes.com/main.asp?SectionID=9&SubSectionID=9&ArticleID=11294http://www.lakelandtimes.com/main.asp?SectionID=9&SubSectionID=9&ArticleID=11294

The CDC then convened officials of the CDC, FDA, AAP, IOM, BigPharma, and BigPharm-affiliated academics to attend a secret (until FOIA-exposed) 7 June 2000 CDC Simpsonwood Conference. They agree to hide from the public the incriminating findings of the CDC Vaccine Safety Datalink and the proceedings of the conference (Robert Chen, CDC: “embargoed information”. Roger Bernier, CDC: “We have been able to manage to keep it out of, let’s say, less responsible hands”) They also agree “further work” be done on the database until no thimerosal-autism link is found.

Those aware of this collusion include the then-CDC-head Gerberding, now President of Merck Vaccines, and the then-CBER-head Jesse Goodman, now FDA “Chief Scientist”.

CDC Simpsonwood Conference Proceedings obtained through the FOIA:
HYPERLINK “http://www.safeminds.org/government-affairs/foia/Simpsonwood_Transcript.pdfhttp://www.safeminds.org/government-affairs/foia/Simpsonwood_Transcript.pdf

After the conference, the CDC withheld Dr. Verstraeten’s findings, although they had been slated for immediate publication. The CDC also told other scientists that Verstraeten’s original data had been ‘lost’ and could not be replicated. To thwart the Freedom of Information Act,
the CDC handed its database of vaccine records over to a private company, declaring it off-limits to researchers.
HYPERLINK “http://en.wikipedia.org/wiki/2000_Simpsonwood_CDC_conferencehttp://en.wikipedia.org/wiki/2000_Simpsonwood_CDC_conference

Letter of Congressman Dave Weldon, M.D., to Gerberding
HYPERLINK “http://www.autismhelpforyou.com/EXPERT%20PAPER%20-%20Weldon%20To%20CDC%20-%20Internet%20File.pdfhttp://www.autismhelpforyou.com/EXPERT%20PAPER%20-%20Weldon%20To%20CDC%20-%20Internet%20File.pdf

In 2003, a private contractor would testify before congress that, in the interest of “patient confidentiality”, he was ordered by the CDC to destroy the original data sets used in the 1999 version of the study that found a thimerosal-autism link. This Vaccine Safety Datalink is eventually moved to an offshore private company and can no longer be accessed
by an FOIA request.
HYPERLINK “http://adventuresinautism.blogspot.com/2005/08/beginning-at-beginning.htmlhttp://adventuresinautism.blogspot.com/2005/08/beginning-at-beginning.html

HYPERLINK “http://www.salon.com/news/feature/2005/06/16/thimerosal/print.htmlhttp://www.salon.com/news/feature/2005/06/16/thimerosal/print.html

IOM Immunization Safety Review Committee

“In 2001 the Institute of Medicine is commissioned by the CDC to undertake a comprehensive review of all research into the thimerosal/autism connection. At their first meeting, Dr [Kathleen] Stratton, head of the commission, when discussing what the process and product of the working group would be states that, “We said this before you got here, and I think we said this yesterday, the point of no return, the line we will not cross in public policy is to pull the vaccine, change the schedule. We could say it is time to revisit this, but we would never recommend that level. Even recommending research is recommendations for policy. We wouldn’t say compensate, we wouldn’t say pull the vaccine, we wouldn’t say stop the program”. When the transcript of the meeting is made public through an FOIA request, many interpret this to mean that no matter what they find, they will not publicly say that there is any link between the thimerosal and autism. Dr. Harvey Fineberg, head of the IOM, states that this is an incorrect interpretation of the comments, but will not offer any alternate interpretation of what else they could mean.”

“The CDC “wants us to declare, well, that these things are pretty safe,” Dr. Marie McCormick, who chaired the IOM Immunization Safety Review Committee, told her fellow researchers when they first met in January 2001. “We are not ever going to come down that [autism] is a true side effect” of thimerosal exposure. According to transcripts of the meeting, the committee’s chief staffer, Kathleen Stratton, predicted that the IOM would conclude that the evidence was “inadequate to accept or reject a causal relation” between thimerosal and autism. That, she added, was the result “Walt wants” – a reference to Dr. Walter Orenstein, director of the National Immunization Program for the CDC.”

In May 2004, the IOM Immunization Safety Review Committee recommends that no further research into the possibility of a thimerosal-autism link be supported, and it then disbands.
HYPERLINK “http://adventuresinautism.blogspot.com/2005/08/beginning-at-beginning.htmlhttp://adventuresinautism.blogspot.com/2005/08/beginning-at-beginning.html
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IV. The Precautionary Principle and the Childhood Immunization Schedule

A. Current CDC Childhood Immunization Schedule

In the 1930’s, the average child received 3 vaccines
HYPERLINK “http://adventuresinautism.blogspot.com/2005/08/beginning-at-beginning.htmlhttp://adventuresinautism.blogspot.com/2005/08/beginning-at-beginning.html

By 2009, the CDC Childhood Immunization Schedule has grown to 37 antigens by the age of 18 months, and 49 by the age of 4 years, starting with an inoculation on the day of birth against Hepatitis B, a sexually-transmitted disease (because teen-agers are too hard to reach, and infants are a captive audience – Sam Katz, conflicted CDC Advisory Committee Chairman, 1991) HYPERLINK “http://www.cdc.gov/mmwr/preview/mmwrhtml/mm5751a5.htm?s_cid=mm5751a5_ehttp://www.cdc.gov/mmwr/preview/mmwrhtml/mm5751a5.htm?s_cid=mm5751a5_e

Virtually every vaccine on this schedule was approved and recommended for inclusion by the members of a heavily-conflicted CDC Advisory Committee on Immunization Practices (ACIP).

A partial list of the untested individual and combined risks from this schedule:

The constantly growing number of childhood vaccine doses, now 49, by the age of four, including 13 antigens at one time at 15 months.

The neurotoxic aluminum adjuvant in a steadily increasing number of vaccines (now 17) and in increasing amounts
By 1983, children were already receiving 5 doses of injected aluminum by 2 years. By 2009, the number has reached 18 doses by 18 months.
The FDA limits IV solutions to 25 mcg (or .025 mg) because aluminum was causing neurological delays in premature babies and dementia in kidney dialysis patients. The toxic dose of aluminum for infants is 10 – 20 mcg. The Hepatitis B Vaccine given to newborns contains 250 mcg. Also, depending on the brand of vaccines given, at a typical 2-month-old checkup a child receives anywhere from 295mcg – 1225mcg, and these vaccines are repeated at 4 and 6 months.
Vaccine Book by Robert Sears, M.D.
HYPERLINK “http://www.thinktwice.com/aluminum.pdfhttp://www.thinktwice.com/aluminum.pdf

Other neurotoxic pediatric vaccine additives, such as formaldehyde and glutamate
Aluminum, formaldehyde, glutamic acid-monosodium salt are all classified as neurotoxins:
HYPERLINK “<a href="http://www.neuroassist.com/Neurotoxins.htm&quot; http://www.neuroassist.com/Neurotoxins.htm”&gt;http://www.neuroassist.com/Neurotoxins.htm” http://www.neuroassist.com/Neurotoxins.htm
HYPERLINK “http://en.wikipedia.org/wiki/List_of_vaccine_ingredientshttp://en.wikipedia.org/wiki/List_of_vaccine_ingredients

Starting in 1990, a permanent increase in the potency of the MMR vaccine
HYPERLINK “http://chanceforchange.wordpress.com/2009/01/15/why-we-fear-the-mmr-vaccine/http://chanceforchange.wordpress.com/2009/01/15/why-we-fear-the-mmr-vaccine/

Starting in 1994, a second dose of the MMR vaccine

Viral contaminants, such as PCV-1 and PCV-2 in the RotaTeq vaccine
HYPERLINK “http://www.nvic.org/NVIC-Vaccine-News/May-2010/VACCINE-CONTAMINATION–A-THREAT-TO-HUMAN-HEALTH.aspx http://www.nvic.org/NVIC-Vaccine-News/May-2010/VACCINE-CONTAMINATION–A-THREAT-TO-HUMAN-HEALTH.aspx

The ongoing exposure of children and fetuses to thimerosal through the CDC-AAP-recommendation of annual thimerosal-preserved flu shots for children and pregnant women
HYPERLINK “http://www.opednews.com/articles/opedne_evelyn_p_050902_fda_knew_dangers_of_.htm” http://www.opednews.com/articles/opedne_evelyn_p_050902_fda_knew_dangers_of_.htm

The untested combined impact of all these risks

B. “Benefit vs. Risk Assessment” of the Childhood Immunization Schedule

The claim by the Vaccine Establishment that its “benefit-vs-risk assessment” of the Childhood Immunization Schedule is overwhelmingly favorable and therefore fully justifies its unquestioning and enthusiastic use is inherently baseless. A truly legitimate benefit-vs-risk assessment of any protocol requires one to first have a reasonably full knowledge of the nature and magnitude of all of its risk(s), including its combined risks. Even if each vaccine, separately, in the Childhood Immunization Schedule were to be accorded a favorable benefit-vs-risk assessment, there is no legitimate way to extrapolate from this that the same must hold true for an entire inoculation protocol. THE ENTIRE CHILDHOOD IMMUNIZATION SCHEDULE HAS NEVER BEEN TESTED FOR SAFETY, so the Vaccine Establishment is ignorant of the impact of the combined risks of this complex protocol. The reassuring “benefit-vs-risk assessment” of this vaccination protocol trumpeted by the Vaccine Establishment to the public is a medical fraud.

With the development of growing parental alarm and opposition, the Vaccine Establishment,
in another propaganda ploy – “for the greater good” – now rationalize the medical necessity of court and legislative mandates to enforce their practice of medicine on U.S. children, thereby trashing U.S. parents’ freedom of choice over the health of their children.
HYPERLINK “http://www.vaccinationnews.com/Scandals/Jun_17_10/Scandal96.htmhttp://www.vaccinationnews.com/Scandals/Jun_17_10/Scandal96.htm

In dealing with dissenters, the Vaccination Establishment and its supporters label vaccination safety critics, distraught parents, and dissident scientists and physicians, all of whom urge greater caution, as anti-vaccination, anti-child-health, ignoramuses and quacks (and similar epithets).

C. Precautionary Principle and Testing the Safety of the Childhood Immunization Schedule

The Precautionary Principle dictates that, except in an emergency situation or when no other course of action is possible, any proposed medical course of action of potential harm must first be tested for safety. Complying with this principle is imperative when the subjects involved are infants and children and when the nature of the risk includes the possibility of their permanent neurological damage. The entire Childhood Immunization Schedule has never been tested for safety using as controls never-inoculated children. CDC officials, Insel’s stacked IACC Committee and the NVAC
Committee have over the years stonewalled such a proposal – whether a retrospective one, with absolutely no “unacceptable health risk”, or a prospective one, for which control groups already exist.
HYPERLINK “http://www.infowars.com/articles/science/autism_none_for_unvaccinated_amish.htmhttp://www.infowars.com/articles/science/autism_none_for_unvaccinated_amish.htm
HYPERLINK “http://iacc.hhs.gov/events/2009/full-committee-mtg-minutes-july15.shtml” http://iacc.hhs.gov/events/2009/full-committee-mtg-minutes-july15.shtml

The outcome of such a study is potentially so catastrophic to the Vaccine Establishment’s repeated assurances that, under all conditions, “there is absolutely no vaccination-autism link”
that they have done everything in their power to keep such a study from being carried out.
So far, they have fully succeeded. Instead, they have proceeded headlong in the exercise of their power and vaccination zeal to fully implement the Childhood Immunization Schedule, trashing the application of the Precautionary Principle for the testing of its safety. FOR OVER THREE DECADES, THEY HAVE HAD IT COMPLETELY THEIR WAY.

HYPERLINK “http://www.generationrescue.org/pdf/special_report_autism2.pdfhttp://www.generationrescue.org/pdf/special_report_autism2.pdf

—————————————————————————————————————-
Like the rest of the medical profession, the Vaccine Establishment, too, has an ethical and professional responsibility and obligation to uphold “First Do No Harm” and the Precautionary Principle. Had they upheld these principles, the Vaccine Establishment could have conducted
the efficacious vaccination of children in as responsible a manner as possible.

The Vaccine Establishment – conflicted and colluding trashers of “First Do No Harm” and
the Precautionary Principle. Their legacy – the unprecedented Autism Epidemic.
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May 2, 2010

Cause Of Autism Found!

UPDATED

Can you say chemical / heavy metal poisoning?
Do these kids even have autism or do we have an epidemic of chemical / heavy metal poisoning? One of the ‘symptoms’ of chemical / heavy metal poisoning is…. DRUM ROLL PLEASE … AUTISM!!!

For whatever the reason, you still have people out there in the world who must live under a rock because they babble the total ‘lame stream corporate media’ lie that mercury (Hg) has been eliminated from vaccines since the early 2000’s. THIS IS A OUTRIGHT FALSEHOOD! Please ask for the flu shot inserts and READ FOR YOURSELF. Mercury is in flu shots, MANY TIMES HIGHER then what was ever put into the MMR vaccine. There are also trace amounts of Hg in other vaccines.
However, Aluminum is a heavy metal that is just as toxic to the body as mercury, and it’s in all the vaccines.
READ THE LABELS PEOPLE!
—————————————————

No matter what ‘MedSpeak’ (works just like Lawyer speak) the Medical Industrial Complex uses to convince us all they haven’t a clue as to how on earth we got ALL these autistic kids and, NOW, adults all around us. Allow me to put 1 +1 together for them. Without all the ‘medspeak’ circular arguments, JUST SCIENTIFIC FACTS. Why do these kids with sever autism rock back and forth? Read through all, find out the answer and a whole lot more. This information IS sourced below HOWEVER, the EPA ALSO backs up these sources as well.

1 Structural and Functional Abnormalities associated with various heavy metal toxins:

Speech and Language Deficits:

Speech disorders
Aluminum, Mercury

Loss of speech, developmental problems with language
Mercury

Speech comprehension deficits
Mercury

Dysarthria; articulation problems; slurred speech, unintelligible speech
Mercury

Cognitive Impairments:

Attentional problems (ADHD), lacks eye contact, impaired visual fixation
Lead, Mercury

Mental retardation, borderline intelligence
Arsenic, Lead, Mercury

Poor concentration, attention deficits (ADHD), response inhibition
Aluminum, Lead

Poor memory (short term, verbal, and auditory)
Aluminum, Lead

Difficulties understanding abstract ideas; difficulty carrying out complex commands
X Metals

Dementia; pre-senile and senile dementia
Aluminum

Stupor
Aluminum, Arsenic

Sensory Abnormalities:
Hearing loss, difficulty hearing
Arsenic, Lead, Mercury

Blurred vision; sensitivity to light
Arsenic, Mercury

Motor Disorders:
Choreiform movements, myoclonal jerks, unusual postures
Copper, Mercury

Difficulty walking, swallowing, talking
Copper, Mercury

Flapping, circling, rocking, toe walking
Mercury

Problems with intentional movements or imitation
Mercury

Abnormal gait/posture; incoordination, loss of balance; problems sitting, lying, crawling, and walking
Mercury

Decreased locomotor activity
Aluminum, Arsenic

Convulsions; seizure
Aluminum , Arsenic, Copper, Lead, Mercury, Thallium

Physiological Impairment
Brain and Central Nervous System:

Neurofibrillary tangles
Aluminum

Neuritis, retrobulbar neuritis; neuropathy
Aluminum, Arsenic, Thallium

Encephalopathy
Aluminum, Arsenic, Lead, Thallium

Accumulates in CNS structures
Aluminum, Mercury

Autonomic disturbances
Copper, Lead, Mercury, Thallium

Peripheral Nervous System:

Peripheral neuropathy
Arsenic, Mercury

Other Physical Disturbances:
Rashes, contact dermatitis, eczema, itchy/irritating skin
Aluminum, Arsenic, Copper, Mercury

Source

Fluoride Poisoning (Yes, Fluoride is in some vaccines)
ADHD/Learning Disorders (4,7)

Allergies (2)

Alzheimer’s Disease (5,6,46)

Anaphylactic Shock (life-threatening, allergic reactions) (2)

Asthenia (Weakness) (18)

Asthma (the loss of full control of bodily movements.) (2)

Autism (169) Gee, you think?

Behavioural Problems (3)

Cachexia (wasting away)(2)

Crying easily for no apparent reason (18)

Demyelinizing Disease (Where the myelin sheath of neurons is damaged) (2, 35)

Depression (8)

Epilepsy (2)

Eosinophilia (blood disorder also associated with some types of leukemia) (15)

Eye, ear and nose disorders (8)

Fibromyalgia (2)

Fibrosis (3)

Hyperparathyroidism (2)

Incoherence (8)

Inner Ear Disorders (2,5)

Lack of Co-ordination (2)

Loss of Appetite (2)

Loss of IQ (25)

Low Birth Weight (5)

Lupus (3)

Magnesium Deficiency (2

Memory Loss (13)

Mental Confusion (20)

Schizophrenia (18)

Seizures (13)

Sensitive to light (1,17)

1) Meiers P – “Zur Toxizität von Fluorverbindungen, mit besonderer
Berücksichtigung der Onkogenese”, Verlag für Medizin Dr. Ewald Fischer, Heidelberg (1984)

2) Waldbott GL, Burgstahler AW, McKinney HL – “Fluoridation:The Great Dilemma” Coronado Press (1978)

3) Yiamouyiannis J – “Fluoride – The Aging Factor”, 3rd. Edition, Health Action Press, 6439 Taggart Road, Delaware, Ohio (1993)

4) Mullenix PJ, Denbesten PK, Schunior A, Kernan WJ – “Neurotoxicity of Sodium Fluoride In Rats” Neurotoxicology and Teratology, 17(2):169-177(1995)

5) Judd, G – “Good Teeth Birth To Death”, Research Publications, Glendale Arizona (1997), EPA Research #2 (1994)

6) Varner JA, Jensen KF, Horvath W, Isaacson RL – “Chronic administration of aluminum- fluoride or sodium-fluoride to rats in drinking water: alterations in neuronal and cerebrovascular integrity” Brain Research 784 284-298 (1998)

7) Zhao LB, Liang GH, Zhang DN, Wu XR – “Effect of high fluoride water supply on children’s intelligence” Fluoride 29 190-192 (1996)

8) Grimbergen GW -“A Double Blind Test for Determination of Intolerance to Fluoridated Water (Preliminary Report)” Fluoride 7:146-152 (1974)

13)Roholm, K.; Fluorine Intoxication – “A Clinical Hygiene Study, With A Review Of the Literature And Some Experimental Investigations” H.K. Lewis & Co., London (1937)

15)Hillman, D; Bolenbaugh, D.L;Convey E.M. -“Hypothyroidism and anemia related to fluoride in dairy cattle” J Dairy Sci 62(3):416-23 (1979)

17)Visnerevski, V – Gig Tr Prof Zabol 13:60 (1969)

18)Spira, L:”The Drama of Fluorine – Arch Enemy of Mankind” Milwaukee Press (1953) (Compilation of published articles)

20)Smith, MC- J Dent Res 14:139 (1934)

25)Li, X.S., Zhi, J.L., and Gao, R.O. “- Effect of fluoride exposure on intelligence in children” Fluoride 28 (1995)

35)Franke, J;Rath, F;Runge, H;Fengler, F;Auermann, E;Lenart G. – “Industrial Fluorosis” Fluoride 8:61-85 (1975)

46)May, W – “Behandlung der Hypothyreosen einschließlich des schweren genuinen Morbus Basedow mit Fluor” Klin Wochenschr 16:562-564 (1937)

169) Cathy Rookard, Director, ACIDD Association for Children and Infants with Digestive Disorders.

Formaldehyde (YES! Also in vaccines)

Chronic formaldehyde exposure at very low doses has been shown to cause immune system and nervous system changes and damage as well as headaches, general poor health, irreversible genetic damage, and a number of other serious health problems (Fujimaki 1992, He 1998, John 1994, Liu 1993, Main 1983, Molhave 1986, National Research Council 1981, Shaham 1996, Srivastava 1992, Vojdani 1992, Wantke 1996)

+1 Autism Symptoms: A complex ‘neurobiological disorder’.

Significant problems developing nonverbal communication skills, such as eye-to-eye gazing, facial expressions, and body posture.

Delay in, or lack of, learning to talk.

depression,

anxiety,

epilepsy

attention deficit hyperactivity disorder (ADHD).

unusual sensory perceptions. (For example, they may describe a light touch as painful and deep pressure as providing a calming feeling.)

Sleep problems (occur in about 40% to 70% of people with autism.)

Source

=2 CAUSE!

Mercury, Aluminum, Fluoride and Formaldehyde are ALL neurological toxins’ to humans and give rise to the very symptoms autistic individuals have. THERE IS NO DEBATING THE NEUROLOGICAL DAMAGE FROM THESE NEURO-TOXINS!!! ONLY when they are in vaccines do these neuro-toxins REINVENT themselves by the vaccine pushers as “HARMLESS”! AND, THEY ARE ALL IN VACCINES!!!!

When will a majority of people finally stand up and say enough is enough?. Kids are NOT inhaling, absorbing through their skin, or ingesting these neuro-toxins but, GETTING THEM INJECTED RIGHT INTO THEIR VEINS!!! All these neuro-toxins are bad enough by themselves but, combined and mixed together with viruses?!! Is it any wonder these kids (now adults) are literally losing or HAVE lost their minds, and or, central nervous system. Do we really need to shovel truckloads of money off some where looking for answers while scratching our heads wondering how this has ALL OF THE SUDDEN HAPPENED?

Why don’t we as a people do this. Stop these vaccines and see what happens when we are NOT injecting this poison into babies and children? I’d take my chances with measles before being lobotomized by toxic vaccine sludge any day!

I remember growing up with family and their friends who all worked with asbestos and that it effected different people differently. Some displayed severe symptoms of poisoning while others didn’t seem effected at all. I bring this up because the vaccine cult tries to imply a slick but, yet bogus and VERY DECEPTIVE claim that, if the neuro-toxic metals and chemicals used in vaccines caused the very neuro-degenerative effects to the human body THEY ARE KNOWN TO CAUSE, ‘ALL’ children would show the same side effects. Unfortunately for the vaccine cult, it does NOT work that way in the ‘real world’.

An independent film crew did a in-depth special on the first sea voyage to attempt to cross the Arctic Circle by ship. This documentary contains EXTREMELY IMPORTANT INFORMATION in understanding autism as a side effect of neuro-toxic poisoning. In the documentary it was WELL RECORDED AND DOCUMENTED that the neuro-degenerative poisoning of the crew did NOT occur in a EQUAL AND EVEN ‘ONE SIZE FITS ALL’ distribution. As a matter of fact, the scientists were ALL in agreement that when the first crew members became ill and died, had the expedition been halted at that time or just before. Some of the crew who ingested the same amount of lead toxicity WOULD HAVE SHOWN NO SIDE EFFECTS WHAT-SO-EVER while other members would have shown ‘A SPECTRUM’ of poisoning. From the dead at one end to, no apparent effect what-so-ever at the other end of the spectrum. This is exactly what you see in the case of autism. However, the crew of the ship at least didn’t have the lead injected into their veins. They simply ingested trace amounts, for their tin food cans and water storage were sealed with lead.

This is the very reason why the vaccine ‘schedule’ issue is a null and void useless issue until the toxins are removed from the vaccines. However, even with the metal and chemical toxins removed you still have the issue of stealth, lab and cancer viruses to have to deal with.

Below is a link where Dr. Blaylock debunks the crazy UNSCIENTIFIC claim of “acceptable exposure” to neuro-toxins.
ACCEPTABLE EXPOSURE MYTH / DISINFO

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