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VRM: The Rise of Mutagenic Viruses

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According to the vanguard of the Vaccine Industry, Vaccinations containing live attenuated viruses have provided relief from numerous fatal diseases in the past, and continue to protect countless people today. In contrast to inactivated vaccines (where-in the viral component is purportedly “killed” via chemical/heat-treatment or exposure to gamma-rays), live attenuated vaccines have the benefit of a more efficient cellular and humoral immune response with a low, sometimes single dose. Thus far, however, live attenuated vaccines have had two major pitfalls.
 
 
 
 
Notably, all viruses are distinguished by their inability to reproduce on their own. ‘They infect the cells of living organisms from plants to people, hijacking the host’s cellular machinery to reproduce itself.
 
In terms of current viral vaccine production, most live viruses undergo a process of modification (attenuation) in a laboratory (in vitro), a procedure designed “ostensibly” to weaken (alter the composition of) the live virus enough, thereby retaining a safe variant of the viral strain (genome), hence providing the human body a tactical blueprint or template of the contagion.
 
The viral isolate is harvested in select animal cell substrates, via a form of reverse engineering. Typical ‘non-natural animal hosts‘ include chick embryos, quail eggs, dog spleens (ie. Cocker Spaniel), diseased & dissected monkey kidneys (spawned Simian Virus 40/SV40), insect viral vectors.
 
The preparation is then loaded into vials, alongside a myriad of toxic excipients, where-upon the “serum” is injected either subcutaneously or intramuscularly into the vaccinee, enters the blood stream directly (bypassing the body’s primary line of defence – nasal passages/mucosal membrane & gastro-intestinal tract), thereby “theoretically” harnessing one’s inherent (natural) defence mechanisms without purposely or inadvertently spreading the actual disease/infection itself – which rapidly unleashes sufficient antibodies to combat the infection, in order to generate a robust immune response & thus immunize the host against the potential viral threat.

       
This process, in fact, the entire methodology behind vaccination as a means of supporting  the Immune system, represents a fundamental flaw in scientific reasoning; verified by the legacy of ineffectiveness, co-infection & cross-contamination associated with the majority of vaccine uptake.

No virus that causes disease in humans has ever been known to mutate to change its mode of transmission.‘ Mainstream Media misinformation

In truth, no virus is fully modified or attenuated or killed during the vaccine manufacturing process. All vaccines, by their very nature, play off each other, generate a “synergistic” chain-reaction triggering further (more insidious) infections & disorders. In many cases the very signature disease/disorder they claim to protect you against is PRECISELY that which they inadvertently spread; albeit a more virulent “transforming” strain of the primary pathogen.

Essentially, ALL Viral vaccines become “weaponized” through the various stages of Vaccine development; further metastasizing in the vaccine host: ‘Mutations that can occur when the vaccine virus replicates in the body may result in more a virulent strain.

In practical terms, a synergy factor inevitably occurs when multiple ingredients such as heavy metals, live (attenuated/modified) viruses/or strands of DNA-RNA “heat treated virus”, antibiotic(s), formaldehyde, detergent(s), diploid cells (aborted fetal tissue), mycoplasma, phenol dye & excipient buffers are combined together in a vial mixture, generating a bio-active (electrical) chemical reaction – worsened by combinations with post-vaccination Prescription drugs; frequently seen as the tipping point which triggers/hastens an escalation of adverse neurological symptoms, a cascading degeneration (reduced Mitochondrial & Metabolic capacity) leading to varying degrees of auto-immune (multi-systemic) failure in the body.

Through the annals of history, outbreaks of disease, plague & life-threatening epidemics were primarily the result of over-crowding, marked by insufficient hygiene, sanitation & nutrition. In this day & age, given proper access to clean drinking water, modern sanitation methods & a steady organic diet, there is simply no excuse, here in the West, for the exponential surge in cases of early childhood diseases & disorders now gripping our communities.   
 
The Vaccine Industry is literally at war with natural immunity, having unleashed a plethora of rogue (hybrid/rarified) early childhood cancers, virulent “chimera” (weaponized/mutagenic) viruses, antibiotic resistant bacterium (ie. Methicillin-resistant Staphylococcus aureus/MRSA) & insidious fungal pathogens (ie. Gut Flora, Candida) upon our youngest & most vulnerable; including a cat’s cradle of neurodevelopmental disorders such as of Autism, ADD, ADHD – marked by chronic illness & compromised immunity, a rash of auto-immune breakdown related issues (ie. prolonged food/environmental allergies) & debilitating behavioral difficulties. 
 
The current generation have become unwitting hosts to a form of viral, bacterial & fungal roulette,  an ideal breeding ground for the proliferation of lifelong (inter-generational) viral, bacterial & fungal (gut related) infections.
 
The overwhelming body of scientific evidence points to one critical determining factor in the rise of mutagenic viruses & systemic erosion of natural immunity: multi-generational community-wide exposure to the Standard Immunization regime, in particular, those viral vaccines fixed on the schedule which combine multiple live attenuated viruses.    

The viruses are generally attenuated on the basis of only a few mutations and have a considerable chance of reverting to wild-type thereby causing the very disease in vaccine recipients that they are aimed to prevent.‘ GIT Laboratory Journal

Despite the advantages of live, attenuated vaccines, there are some downsides. It is the nature of living things to change, or mutate, and the organisms used in live, attenuated vaccines are no different. The remote possibility exists that an attenuated microbe in the vaccine could revert to a virulent form and cause disease.’ US National Institute of Allergy and Infectious Diseases

One concern that must be considered is the potential for the vaccine virus to revert to a form capable of causing disease. Mutations that can occur when the vaccine virus replicates in the body may result in more a virulent strain. This is very unlikely, as the vaccine virus’s ability to replicate at all is limited; however, it is taken into consideration when developing an attenuated vaccine.

It is worth noting that mutations are somewhat common with the oral polio vaccine (OPV), a live vaccine that is ingested instead of injected. The vaccine virus can mutate into a virulent form and result in rare cases of paralytic polio. For this reason, OPV is no longer used in the United States, and has been replaced on the Recommended Childhood Immunization Schedule by the inactivated polio vaccine (IPV).‘ College of Physicians, Philadelphia 

One vaccine decreases cell-mediated immunity by 50%, two vaccines by 70%…all triple vaccines (MMR, DTaP) markedly impair cell-mediated immunity, which predisposes to recurrent viral infections, especially otitis media, as well as yeast and fungi infections.” World-renowned Immunologist Dr. H.H. Fudenberg 

Adventitious agents (mutable viruses/cross-contamination) could theoretically enter a viral vaccine through any of these ingredients (cell substrates, vaccine seed, tissue culture reagents, stabilizers).’ FDA 

Many novel vaccines are produced in animal cell substrates, and emerging infectious diseases may theoretically be transmitted from animals to humans through these vaccines.’ FDA

Vaccines are increasingly becoming ineffective and causing “immune dysfunction. Additionally, “vaccine antigen responses” may be reprogramming viruses (altering the DNA template of the virus – alterations in the ‘Nucleotide sequencing’ of the primary viral strain) while weakening the immune systems of the most vaccinated individuals.’ Dr. Gary Null & Richard Gale       

There is concern that genetic technologies will be used to modify these already pathogenic agents and create “super-pathogens”. DNA shuffling (accelerated or directed molecular evolution) or combining genetic elements of distinct pathogenic viruses to create chimeric viruses, could be applied to bio-weapons enhancement.’ Impact of Synthetic Genomics on the Threat of Bioterrorism with Viral Agents, Marc S. Collett/ViroDefense Inc. 

‘Many live attenuated vaccines for animals (including humans) are manufactured by using cell lines from animals, which are known to produce infectious ‘endogenous retroviruses‘ (Remnants of ancestral exogenous retroviral infections fixed in the germline DNA); however, the risks of infection by ERVs from xenospecies through vaccination have been ignored.’ Laboratory of Signal Transduction, Department of Cell Biology, Institute for Virus Research, Kyoto University

 

When passaged in the laboratory (in either cell culture or lab animals), primary isolates often become attenuated. The attenuation is the result of adaptive genetic changes that the virus acquires in order to survive in its new environment. These genetic changes can be subtle (single nucleotide changes) or dramatic (genome deletions or rearrangements). Generally, the longer a virus is propagated in cell culture, or through non-natural animal hosts, the greater the attenuation. In fact, this is the basic methodology for the development of many live attenuated virus vaccines.’ Impact of Synthetic Genomics on the Threat of Bioterrorism with Viral Agents, Marc S. Collett/ViroDefense Inc.

Why are clusters of measles outbreaks on the rise? It has nothing to do with the increasing trend toward lower rates of vaccine uptake throughout our communities; the inference that avoiding getting your child “immunized” with the MMR series increases their risk of susceptibility to measles and transference of measles to other children in their proximity. As Dr Tetyana Obukhanych Ph.D, one of the world’s leading Immunologists (guest speaker at our recent VRM Vaccine Summit) points out, vaccines have stripped mothers, and by extension, their baby, of the capacity for life-long immuno-protection, given the absence of NATURAL childhood exposure to measles in the environment.

Parents who received the first wave of (live) measles shots in 1963, and all those since, were subsequently stripped of their capacity to transfer natural immuno-protection to their baby, via the Placenta & Colostrum, due to the cross-contamination factor (hybrid measles virus now embedded in the mother/father’s germ line DNA – manifesting in a more virulent strain of measles, known as ‘Atypical Measles‘) generated by the shot, passed on to the new generation.

The current generation have literally become unwitting hosts to a form of viral & bacterial roulette, an ideal breeding ground for the proliferation/weaponizing of viral & bacterial infections.

“I am very concerned that “immunologic memory” of adjuvant-containing vaccines is actually the basis of sensitization rather than the basis of immunity. Furthermore, I am very concerned that “successful” prevention of childhood diseases by means of short-term protective effects of live attenuated viral vaccines during childhood has led to the loss of maternal ability to transfer immuno-protection to their young, thereby leaving infants vulnerable to those diseases, should the exposure occur.

I am also very concerned that vaccination campaigns work by disrupting disease transmission, which reduces the chances of exposure, rather than by establishing a population’s immunity. By doing so, vaccination campaigns wipe out population’s immunity to childhood diseases rather than help to maintain it. If in prior decades there was naturally established herd immunity to childhood diseases among the adult population, then I am afraid that vaccination campaigns have ensured that it is long gone.

All of this is a direct outcome of the “desired” vaccination effects, the impact of which hasn’t been carefully thought through in advance of introducing mass vaccination. We thought that vaccines work just like natural immunity. Well, apparently they don’t and we are now reaping the consequences of that.

We would expect that vaccinated individuals would not be involved (or very minimally involved) in any outbreak of an infectious disease for which they have been vaccinated. Yet, when outbreaks are analyzed, it becomes apparent that most often this is not the case. Vaccinated individuals are indeed very frequently involved and constitute a high proportion of disease cases.

I think this is happening because vaccination does not engage the genuine mechanism of immunity. Vaccination typically engages the immune response—that is, everything that immunologists would theoretically “want” to see being engaged in the immune system. But apparently this is not enough to confer robust protection that matches natural immunity. Our knowledge of the immune system is far from being complete.” Dr Tetyana Obukhanych Ph.D

We found 18 reports of measles outbreaks in very highly immunized school populations where 71% to 99.8% of students were immunized against measles. Despite these high rates of immunization, 30% to 100% (mean, 77%) of all measles cases in these outbreaks occurred in previously immunized students. In our hypothetical school model, after more than 95% of schoolchildren are immunized against measles, the majority of measles cases occur in appropriately immunized children.

While awaiting production and publication of other research, it would not be appropriate to alarm recipients of the vaccine by notifying them of this hypothetical risk, thus jeopardizing an immunization program of proven benefit.’ Identification of Genetic Mutations Associated With Attenuation and Changes in Tropism of Urabe Mumps Virus, Journal of Medical Virology 81:130–138/2009 

Note:  ‘…it would not be appropriate to alarm recipients of the vaccine by notifying them of this hypothetical risk, thus jeopardizing an immunization program of proven (cost) benefit.’
 
 
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