VRM: The Rise of Mutagenic Viruses
‘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.
‘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 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
‘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.
‘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.
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.
“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
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
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