Paul Offit – 10,000 Vaccines In One Day…Vaccine MAD Man



“The Great Vaccine Milenko” –  Paul Offit

I just love Paul Offit. Don’t you? [Sarcasm] Here in this below article there is a video he has done, attempting to explain away any concern as to the thimerosal issue and in regard to the recent American Academy of Pediatrics push to keep thimerosal in all the vaccines used in such as other countries that are underdeveloped. So, to keep getting vaccines available across the globe, there is no other way, we must keep poisoning the infants, children, and adults, with mercury to do that and to provide those vaccines? I can understand that possibly single dose vials may be in reality a bit impractical and or more expensive, but really if that is all we can produce that is safe, then the vaccine makers can just go with less for profits. Poisoning the world with mercury containing vaccines has been going on for far to many years and decades already. In the year 2013, they still have no better option? Or is it just about making the least expensive vaccine in those countries, and profits? There has to be a better option, if they were seriously and actively looking. However, until the CDC the WHO and as well the AAP get on board and admit to the serious dangers of thimerosal nothing can nor likely will happen to change this.

So, in this Offit video right here, what are we actually witnessing? WE are witnessing Mr Offit again being a huge part of the problem by ignoring existing science, and again making denial of any problem with thimerosal. What we need is for him to get honest, for this to actually change. He needs to get it in his head that what he is actually doing is not only wrong, but it is as well a criminal act. To as continue to mislead the public, and all existing believed authorities, and the government/s as well, is additionally another criminal act.

So, they are telling us that they can find no other chemical (a neurotoxic heavy metal), on the planet earth to take the place of thimerosal/ mercury, and no substance to perform the same function in a vaccine??? And we are to actually believe that?

At the end of that article page however even though Offit claims that there are seven studies he is referencing, only this study is referenced to, and is NOT a physiological or epidemiological science study, it is only a their own opinion piece. Just look at what this QUACK gets away with. We all know as well that any of the CDC funded epidemiological studies they reference, were entire corrupt with predetermined outcomes and obvious study design flaws. The several analysis available on those studies, show that how and why that is only and the obvious actually thinking conclusion.


Orenstein WA, Paulson JA, Brady MT, Cooper LZ, Seib K. Global vaccination recommendations and thimerosal. Pediatrics. 2012;131:149-151.

Let’s look at what the reality of some of the real existing science shows us, and a lot of this is also published right in Pubmed, so they obviously can not claim that they are only some obscure studies that do not deserve consideration and further follow up studies. That’s right, studies that were needed already decades ago, funded by the CDC, with as well the participation of unbiased oversight.

Medscape Infectious Diseases > Offit on Vaccines

Thimerosal in Vaccines: What Are the Facts?

Note worthy is as well that at the end of that article page, even though Offit claims that there are seven studies that he is referencing from; only one one, this study below is referenced to. It is as well NOT a physiological or epidemiological science study, it is only a their own opinion piece. Just look at what this QUACK gets away with. We all know as well (should), that any of the CDC funded epidemiological studies they reference, were entirely corrupt with predetermined outcomes and obvious study design flaws. The several analysis available on those studies, show that how and why that is only and the obvious actually thinking conclusion.

Offit’s article listed – References, (one single reference)

Orenstein WA, Paulson JA, Brady MT, Cooper LZ, Seib K. Global vaccination recommendations and thimerosal. Pediatrics. 2012;131:149-151.

This below study, (Mr Offit); shows that even though ethyl mercury may be detoxed more quickly as far as the amount leaving the body; the study shows that both ethyl mercury and methyl mercury are still a significant concern as to potential toxicity. As well just because ethyl mercury left the body quicker, that would not tell you what level of mercury was left in the tissues, organs, and the brain. Such statements would as well clearly not take in account the children and adults who produce less that adequate levels of glutathione necessary to detox that ethyl mercury.

Arch Toxicol. 1985 Sep;57(4):260-7.

The comparative toxicology of ethyl- and methylmercury.

Magos L, Brown AW, Sparrow S, Bailey E, Snowden RT, Skipp WR.


Neurotoxicity and renotoxicity were compared in rats given by gastric gavage five daily doses of 8.0 mg Hg/kg methyl- or ethylmercuric chloride or 9.6 mg Hg/kg ethylmercuric chloride. Three or 10 days after the last treatment day rats treated with either 8.0 or 9.6 mg Hg/kg ethylmercury had higher total or organic mercury concentrations in blood and lower concentrations in kidneys and brain than methylmercury-treated rats. In each of these tissues the inorganic mercury concentration was higher after ethyl- than after methylmercury. Weight loss relative to the expected body weight and renal damage was higher in ethylmercury-treated rats than in rats given equimolar doses of methylmercury. These effects became more severe when the dose of ethylmercury was increased by 20%. Thus in renotoxicity the renal concentration of inorganic mercury seems to be more important than the concentration of organic or total mercury. In methylmercury-treated rats damage and inorganic mercury deposits were restricted to the P2 region of the proximal tubules, while in ethylmercury-treated rats the distribution of mercury and damage was more widespread. There was little difference in the neurotoxicities of methylmercury and ethylmercury when effects on the dorsal root ganglia or coordination disorders were compared. Based on both criteria, an equimolar dose of ethylmercury was less neurotoxic than methylmercury, but a 20% increase in the dose of ethylmercury was enough to raise the sum of coordination disorder scores slightly and ganglion damage significantly above those in methylmercury-treated rats.

A case series of children with apparent mercury toxic encephalopathies manifesting with clinical symptoms of regressive autistic disorders.


J Toxicol Environ Health A. 2007 May 15;70(10):837-51.

A case series of children with apparent mercury toxic encephalopathies manifesting with clinical symptoms of regressive autistic disorders.

Geier DA, Geier MR.

Source:Institute of Chronic Illnesses, Inc., Silver Spring, Maryland, USA.


Impairments in social relatedness and communication, repetitive behaviors, and stereotypic abnormal movement patterns characterize autism spectrum disorders (ASDs). It is clear that while genetic factors are important to the pathogenesis of ASDs, mercury exposure can induce immune, sensory, neurological, motor, and behavioral dysfunctions similar to traits defining or associated with ASDs. The Institutional Review Board of the Institute for Chronic Illnesses (Office for Human Research Protections, U.S. Department of Health and Human Services, IRB number IRB00005375) approved the present study. A case series of nine patients who presented to the Genetic Centers of America for a genetic/developmental evaluation are discussed. Eight of nine patients (one patient was found to have an ASD due to Rett’s syndrome) (a) had regressive ASDs; (b) had elevated levels of androgens; (c) excreted significant amounts of mercury post chelation challenge; (d) had biochemical evidence of decreased function in their glutathione pathways; (e) had no known significant mercury exposure except from Thimerosal-containing vaccines/Rho(D)-immune globulin preparations; and (f) had alternate causes for their regressive ASDs ruled out. There was a significant dose-response relationship between the severity of the regressive ASDs observed and the total mercury dose children received from Thimerosal-containing vaccines/Rho (D)-immune globulin preparations. Based upon differential diagnoses, 8 of 9 patients examined were exposed to significant mercury from Thimerosal-containing biologic/vaccine preparations during their fetal/infant developmental periods, and subsequently, between 12 and 24 mo of age, these previously normally developing children suffered mercury toxic encephalopathies that manifested with clinical symptoms consistent with regressive ASDs. Evidence for mercury intoxication should be considered in the differential diagnosis as contributing to some regressive ASDs.

Pubmed index of more related studies
Evidence of Parallels Between Mercury Intoxication and the Brain Pathology in Autism

The Severity of Autism Is Associated with Toxic Metal Body Burden and Red Blood Cell Glutathione Levels


This study investigated the relationship of children’s autism symptoms with their toxic metal body burden and red blood cell (RBC) glutathione levels. In children ages 3–8 years, the severity of autism was assessed using four tools: ADOS, PDD-BI, ATEC, and SAS. Toxic metal body burden was assessed by measuring urinary excretion of toxic metals, both before and after oral dimercaptosuccinic acid (DMSA). Multiple positive correlations were found between the severity of autism and the urinary excretion of toxic metals. Variations in the severity of autism measurements could be explained, in part, by regression analyses of urinary excretion of toxic metals before and after DMSA and the level of RBC glutathione (adjusted in all cases). This study demonstrates a significant positive association between the severity of autism and the relative body burden of toxic metals.

Oxidative Stress Causes Renal Dopamine D1 Receptor Dysfunction and Hypertension via Mechanisms That Involve Nuclear Factor-?B and Protein Kinase C

Low natural killer cell cytotoxic activity in autism: The role of glutathione, IL-2 and IL-15

Oxidative stress in autism

NYS Institute for Basic Research in Developmental Disabilities

Excerpt: Several studies have suggested alterations in the activities of antioxidant enzymes such as superoxide dismutase, glutathione peroxidase, and catalase in autism. Additionally, altered glutathione levels and homocysteine/methionine metabolism, increased inflammation, excitotoxicity, as well as mitochondrial and immune dysfunction have been suggested in autism

Cellular and mitochondrial glutathione redox imbalance in lymphoblastoid cells derived from children with autism

Excerpt: These results suggest that the autism LCLs exhibit a reduced glutathione reserve capacity in both cytosol and mitochondria that may compromise antioxidant defense and detoxification capacity under prooxidant conditions.

Neurotoxicology. 2005 Jan;26(1):1-8.

Thimerosal neurotoxicity is associated with glutathione depletion: protection with glutathione precursors.

Neurosurgeon issues public challenge to vaccine zealots: Inject yourselves with all shots you say children should get!


Dr. Russell Blaylock is a board certified neurosurgeon, author and lecturer. He attended the Louisiana State University School of Medicine in New Orleans and completed his general surgical internship and neurosurgical residency at the Medical University of South Carolina in Charleston, South Carolina. During his residency training he worked with the eminent neurosurgeon, Dr. Ludwig Kempe. Together they developed the transcallosal removal of intraventricular tumors, a technique still used today. For the past 25 years he has practiced neurosurgery in addition to having a nutritional practice. He recently retired from his neurosurgical duties to devote his full attention to nutritional studies and neuroscience research.

Published Papers – Dr. Russell Blaylock

Vaccines Contaminated with Mycoplasma’s – by Garth Nicolson microbiologist

Dr. Sherri Tenpenny: What’s Coming Through That Needle

What Is Coming Through That Needle? The Problem of Pathogenic Vaccine Contamination

Benjamin McRearden

Vaccines And Immune Suppression

December 31, 2012

SaneVax: Newly Developed Same-Nested PCR Method May Help Answer Questions Regarding HPV Vaccine Safety

TROY, Mont.–(BUSINESS WIRE)–SaneVax Inc. announces the development of a new PCR methodology described in “Detection of human papillomavirus L1 gene DNA fragments in post-mortem blood and spleen after Gardasil vaccination – A case report,” authored by Dr. Sin Hang Lee of Milford Hospital, Connecticut. This method may provide a way for concerned scientists to determine whether or not HPV vaccines are linked to serious adverse events and death. The study undertaken to develop this method was commissioned and sponsored by SaneVax Inc. for a future payment not to exceed one US dollar, as disclosed in the article.

Read more:

And it is NOT just about the thimerosal (mercury) issue

Aluminum information, toxicity, safety, danger, benefit and risk

From: History of crime against the Food Laws (1929) by Dr. Riley, the prime mover behind the original Pure Food Law and Director of the FDA. He resigned in disgust in 1912 over exceptions granted to the law and lack of enforcement.

Aluminum has been exempted from testing for safety by the FDA under a convoluted logic wherein it is classified as GRAS. (Generally Regarded As Safe.) It has never been tested by the FDA on its safety and there are NO restrictions whatever on the amount or use of aluminum. Diseases Associated with Aluminium Intoxication. H. Tomlinson, M.B., Ch.B., MRCS., LRCP. Since that time thousands of studies have been published indicating aluminum is involved in neurological dysfunction, immunocompetence, as well as a host of other morbidities. I cannot begin to reference them all. Sepsis: a cause of aluminum release from tissue stores associated with acute neurological dysfunction and mortality. Davenport A. – Williams P.S. – Roberts N.B. – Bone J.M. From: Clin Nephrol (1988 Jul) 30(1):48-51. We report six cases of patients with renal failure and exposure to aluminum who developed septicemia. In all cases the serum aluminum increased markedly. This may have contributed to the neurological dysfunction seen in five, and the deaths of four of the patients. We suggest that the rise in serum aluminum was due to the release of tissue-bound aluminum, resulting in an increase in free, diffusable aluminum and that this jeopardized both neurological function and immunocompetence.

Understanding Colloidal Suspensions – Help from Frank Hartman & Thomas Riddick (What does injecting aluminum do to the blood, aluminum is a coagulant, and blood is a fluid)

Vaccine Caused Ischemia/Hypoxia, (the as a fact, now silenced information)


Understanding Colloidal Suspensions – Help from Frank Hartman & Thomas Riddick

Aluminum toxicity is a widespread problem in all forms of life, including humans, animals, fish, plants and trees, and causes widespread degradation of the environment and health. Over 7000 reference articles on aluminum toxicity exist in various data bases; ( as of 1996 ) all recognizing the toxicity but concluding the mechanism of action is unknown. — [ Search results – ]

Aluminum information, toxicity, safety, danger, benefit and risk


Here is of course what the Offit video was based on and what it actually regarded.

Pediatricians: Keep Thimerosal in Vaccines

TRUST …THEM, The American Academy of Pediatrics??? They know whats best, right? They have all the science, right? And do you actually believe that? What a bunch of criminal, sick, and irresponsible, to much to lose, bullshit.


The American Academy of Pediatrics has endorsed the World Health Organization’s stance that thimerosal — a mercury-based preservative — should be left in vaccines and should not be subject to a ban contained in a draft treaty from the United Nations Environment Program (UNEP).

In a brief statement published online in Pediatrics, the academy supported the recommendations drafted by the WHO’s Strategic Advisory Group of Experts (SAGE) on immunization at an April meeting. An AAP spokesperson said that the endorsement was adopted unanimously by the academy’s infectious diseases committee.

The Pediatrics Infectious Diseases Society and the International Pediatric Association have also thrown their support behind the guidance.

Protect Your Children – The AAP and WHO Want to Keep Poisonous Mercury in Vaccines

Petitioning Rep. Darrell Issa

American Academy of Pediatrics (AAP): The AAP must reverse support for unrestricted use of mercury in vaccines.


Federal Response to the Increase in Autisn 1 in 99 (hearings in which the CDC was questioned about the situation. Their responses are of course entirely pathetic)


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