Category Archives: MERCURY/Thimerosal

Aussie PhD candidate’s Authoritative Thesis on the Risks of Vaccination

Welcome

Biography

A CRITICAL ANALYSIS OF THE AUSTRALIAN GOVERNMENT’S RATIONALE FOR IT’S VACCINE POLICY

Judy Wilyman, University of Wollongong

Mass vaccination campaigns were adopted after this time as the central management strategy for preventing infectious diseases, with many new vaccines being recommended in the National Immunization Program (Australia, for example). The implementation of mass vaccination programs occurred simultaneously with the development of partnerships between academic institutions and industry. All member countries of the World Health Organization (WHO), adopt the recommendations made by the Global Alliance for Vaccines and Immunization (GAVI). This is a partnership with the WHO and UNICEF that includes the World Bank, the International Monetary Fund, the International Federation of Pharmaceutical Manufacturers and Associations (IFPMA), the Bill and Melinda Gates Foundation (BMGF),the Rockefeller Foundation, the United Nations Development Fund (UNDF) and other private research institutions.

Introduction (Excerpt)

It is important that independent research is carried out to assess whether all thevaccines being recommended today are safe, effective and necessary for the protection of thecommunity. It is also important to have comprehensive evidence that it is safe to combine multiple vaccines in the developing bodies of infants. The framework for undone science is used to analyse the Australian government’s claim that the benefits of vaccines far outweigh the risks. Whilst the government claims serious adverse events to vaccines are rare this is not supported by adequate scientific evidence due to the shortcomings in clinical trials and long-term surveillance of health outcomes of recipients. A close examination of the ‘Swine Flu’ 2009 vaccine and the vaccine for human papillomavirus (HPV), intended to prevent cervical cancer, shows shortcomings in the evidence base and rationale for the vaccines.

This investigation demonstrates that not all vaccines have been demonstrated to be safe, effective or necessary. It also concludes that the government’s claim that the benefits of vaccines far outweigh the risks cannot be sustained due to the gaps in the scientific knowledge resulting from unfunded research and the inadequate monitoring of adverse events after vaccination.

READ DISSERTATION….

UPDATE: ORCHESTRATED ATTACKS ON JUDY AND THE UNIVERSITY

Excerpts: The outrage over Judy becoming Dr Wilyman can best be understood by studying the operations of the group now calling itself Stop the Australian (Anti)Vaccination Network or SAVN. Since 2009, SAVN has been attempting to censor and discredit any public criticism of vaccination, using misrepresentation, ridicule, complaints and harassment, as I have documented in a series of articles. (Brian Martin)

Study: Conflicts of Interest re: Mercury & Autism Epidemic

no-safevax

Systematic Assessment of Research on Autism Spectrum Disorder and Mercury Reveals Conflicts of Interest and the Need for Transparency in Autism Research.  Read study/Download PDF

  • Janet K. Kern 
  • , David A. Geier
  • , Richard C. Deth
  • , Lisa K. Sykes
  • , Brian S. Hooker
  • , James M. Love
  • , Geir Bjørklund
  • , Carmen G. Chaigneau
  • , Boyd E. Haley

Chronic Mercury Exposure (Dental, Vaccines, Environment) UP 900%

Detectable Mercury in the blood from chronic exposure

Dan Laks, lead author of the study “Assessment of chronic mercury exposure within the U.S. population, National Health and Nutrition Examination Survey, 1999–2006)” analyzed data from the CDC’s National Health Nutrition Examination Survey (NHANES) and found that in the 1999-2000 NHANES survey, mercury was detected in the blood of 2 percent of women aged 18 to 49, that level rose to 30 percent of women by 2005-2006.

Assessment of chronic mercury exposure within the U.S. population, National Health and Nutrition Examination Survey, 1999–2006

Major Study: Adjuvants in Vaccines causing Autoimmune Inflammatory Syndrome (ASIA)

Adjuvant Review Synopsis:

Adjuvants are compounds incorporated into vaccines to enhance
immunogenicity.
• Several of thesemolecules have been approved, including aluminium
salts, oil-in-water emulsions (MF59, AS03 and AF03), virosomes and
AS04.
• Adjuvants have recently been implicated in the new syndrome named
“ASIA—Autoimmune/inflammatory Syndrome Induced by Adjuvants”.
• The pathogenesis of the ASIA syndrome is founded on the hypothesis
that an exposure to an adjuvant may trigger the development of an
autoimmune disease.
• Several different adjuvants exist and each one has specific characteristics
and a different mechanism of action that could affect both the
immune response and the risk of adverse events.
• All available adjuvants, despite their different mechanisms of action,
have been implicated to the ASIA syndrome.
• Our analysis highlights our current understanding of the mechanisms
of action of available adjuvants and the mechanisms by which these
components may determinate autoimmunity.  Adjuvant Review study…

 

VLA Comment: What about the adjuvants in Monsanto’s Round Up, companion to GMO seeds?

herbicide_formulation

Roundup more damaging than glyphosate

There is already evidence that glyphosate is an endocrine disrupting chemical (see later), but the extent of the problem is far greater than it appears. Different glyphosate formulations vary in toxicity, mainly because some of them contain adjuvants that are either toxic by themselves, or else exert synergistic effects with glyphosate. It has long been known that Monsanto’s formulation Roundup, the most widely used glyphosate herbicide, is far more damaging than glyphosate itself (reviewed in [5] Ban GMOs Now, ISIS special report)

…and colleagues at University of Caen in France clearly demonstrated that POEA (polyethoxylated tallowamine, a major adjuvant surfactant in Roundup) alone was by far the most cytotoxic for several human cell types, at concentrations a hundredth to ten-thousandth that of glyphosate itself and other formulations without POEA [6]. Another study from the same laboratory also showed that Roundup exposure damages testosterone producing Leydig cells from mature rat testis at concentrations a tenth of agricultural use and beginning 1 hour after exposure [7]. Within 24-48 h, the same formulation was toxic to other cells inducing cell death, in contrast to glyphosate alone, which is only toxic to Sertoli cells (feeder cells for germ cells). At 48 h, Roundup induces apoptosis (programmed cell death involving DNA fragmentation) in germ cells and in Sertoli/germ cells co-culture. At the very low, non-toxic concentration of 1 ppm, both Roundup and glyphosate decreased testosterone level by 35 %. These experiments expose a major inadequacy in the regulatory regime, which still regards POEA in Roundup as an inert adjuvant for which no risk assessment is required.http://www.i-sis.org.uk/Glyphosate_Roundup_and_Human_Male_Infertility.php

Journal of Toxicology: Thimerosal Induced Mitochondrial Dystfunction AUTISM

mitochondria_labeled Read Abstract & Study

Increased Susceptibility to Thimerosal-Induced Mitochondrial Dysfunction in a Subset of Autism Lymphoblastoid Cell Lines

(Mitochondria Protected by Pre-treatment with the Glutathione Precursor, N-Acetyl Cysteine)

Journal of Toxicology
Volume 2015 (2015), Article ID 573701, 13 pages
http://dx.doi.org/10.1155/2015/573701