{"id":13124,"date":"2014-01-01T13:47:54","date_gmt":"2014-01-01T21:47:54","guid":{"rendered":"http:\/\/vaccineresistancemovement.org\/?p=13124"},"modified":"2016-04-10T08:12:18","modified_gmt":"2016-04-10T16:12:18","slug":"vrm-the-rise-of-mutagenic-viruses","status":"publish","type":"post","link":"https:\/\/vaccineresistancemovement.org\/?p=13124","title":{"rendered":"VRM: The Rise of Mutagenic Viruses"},"content":{"rendered":"

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\"MMR-Vaccination\"<\/a><\/div>\n
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According to the vanguard\u00a0of the Vaccine Industry,<\/strong>\u00a0‘<\/span>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<\/span><\/a>\u00a0(where-in the viral component is purportedly “killed”\u00a0via chemical\/<\/strong>heat-treatment or exposure to gamma-rays)<\/strong>, 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. <\/strong><\/span><\/div>\n
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Firstly, attenuated phenotypes have been produced by either randomly introducing and testing mutations in the viral genomes or by serial passage of the viruses under suboptimal conditions, such as non-natural host cells or low temperatures. These methods often rely on chance and cannot be universally applied to a wide variety of virus types. <\/span><\/a><\/strong><\/div>\n
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Additionally, the extent of viral attenuation, an important consideration for the development of an efficient vaccine, cannot be further manipulated by this method because the molecular mechanism of the attenuation is usually not known. Secondly, 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<\/span><\/strong><\/a>.’ <\/span><\/strong><\/div>\n
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Note: ‘<\/span>Scientists produce inactivated vaccines (ie. Polio Vaccine\/IPV) by killing the disease-causing microbe with chemicals, heat, or radiation. Such vaccines are <\/span><\/a>(ostensibly) <\/span><\/strong>more stable and safer than live vaccines: The dead microbes can\u2019t mutate back to their disease-causing state. Inactivated vaccines usually don\u2019t require refrigeration, and they can be easily stored and transported in a freeze-dried form, which makes them accessible to people in developing countries.<\/span><\/a>‘<\/span><\/strong><\/div>\n
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\"Measles<\/a>A Virus is defined as a microorganism, consisting of strands of RNA\/DNA <\/span><\/strong>‘smaller than a bacterium that cannot grow or reproduce apart from a living cell. A virus invades living cells and uses their chemical machinery to keep itself alive and to replicate itself. It may reproduce with fidelity or with errors (mutations); this ability to mutate is responsible for the ability of some viruses to change slightly in each infected person, making treatment difficult.<\/span><\/strong><\/a>‘ <\/span><\/strong><\/div>\n
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Notably, all viruses are distinguished by\u00a0their\u00a0inability to reproduce on their own. ‘<\/span><\/strong>They infect the cells of living organisms from plants to people, hijacking the host’s cellular machinery to reproduce itself.<\/span><\/strong><\/a>‘<\/div>\n
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In terms of current viral vaccine production, most live viruses undergo a process of\u00a0modification (attenuation) in a laboratory (in vitro), a procedure designed “ostensibly” to weaken (alter the composition of)\u00a0the 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. <\/span><\/strong><\/div>\n
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The viral isolate is\u00a0harvested in select animal cell substrates, via a form of reverse engineering. Typical ‘<\/span><\/strong>non-natural animal hosts<\/span><\/strong><\/a>‘\u00a0include chick embryos, quail eggs, dog spleens (ie. Cocker Spaniel), diseased & dissected monkey kidneys (spawned Simian Virus 40\/SV40),\u00a0insect viral vectors. <\/span><\/strong><\/div>\n
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The preparation is then\u00a0loaded into\u00a0vials, alongside a myriad of toxic<\/span><\/strong> excipients<\/span><\/strong><\/a>,\u00a0where-upon the “serum” is injected either subcutaneously or intramuscularly into the vaccinee, enters\u00a0the blood stream directly (bypassing the body’s primary line of defence –\u00a0nasal passages\/mucosal membrane\u00a0& gastro-intestinal tract), thereby “theoretically” harnessing\u00a0one’s inherent (natural) defence mechanisms without purposely or inadvertently spreading the actual disease\/infection itself – which <\/strong>rapidly unleashes sufficient antibodies to combat the infection, in order to generate a robust immune response &\u00a0thus immunize the host against the potential viral threat.<\/strong><\/span><\/p>\n

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This process, in fact, the entire methodology behind vaccination as a means of supporting\u00a0 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. <\/span><\/strong><\/div>\n
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\"syringe3\"<\/a><\/div>\n

‘No virus that causes disease in humans has ever been known to mutate to change its mode of transmission.<\/a>‘ Mainstream Media misinformation<\/strong><\/p>\n

In truth, no virus is fully modified or attenuated or killed\u00a0during the vaccine manufacturing process. All vaccines, by their very nature, play off each other, generate a \u201csynergistic\u201d 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”\u00a0strain of the\u00a0primary pathogen. <\/span><\/strong><\/p>\n

Essentially,\u00a0ALL Viral vaccines become “weaponized” through the various stages of Vaccine development;\u00a0further metastasizing in the vaccine host<\/a>:\u00a0\u2018Mutations that can occur when the vaccine virus replicates in the body may result in more a virulent strain.<\/a>‘<\/strong><\/p>\n

In practical terms, a synergy factor inevitably occurs when multiple ingredients such as heavy metals, live (attenuated\/modified) viruses\/or strands of DNA-RNA \u201cheat treated virus\u201d, 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\u00a0– <\/strong>worsened by combinations with post-vaccination Prescription drugs; frequently seen as the tipping point which triggers\/hastens\u00a0an escalation of\u00a0adverse neurological symptoms, a cascading degeneration (reduced Mitochondrial & Metabolic capacity) leading to varying degrees of auto-immune (multi-systemic) failure\u00a0in the body. <\/strong><\/span><\/p>\n

Through the annals of history, outbreaks of disease, plague & life-threatening epidemics were primarily the result of over-crowding,\u00a0marked by\u00a0insufficient hygiene, sanitation & nutrition. In this day & age, given proper access to clean drinking water, modern\u00a0sanitation methods\u00a0& a\u00a0steady 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. \u00a0\u00a0<\/span><\/strong><\/div>\n
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The Vaccine Industry\u00a0is literally at war with natural immunity, having\u00a0unleashed a plethora of rogue (hybrid\/rarified) early childhood cancers, virulent “chimera”\u00a0(weaponized\/mutageni<\/span>c) viruses, antibiotic resistant bacterium\u00a0(ie. Methicillin-resistant Staphylococcus aureus\/MRSA)\u00a0&\u00a0insidious fungal pathogens\u00a0(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.\u00a0prolonged food\/environmental allergies) & debilitating behavioral difficulties.\u00a0<\/span><\/strong><\/div>\n
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The current generation have become unwitting hosts to a form of viral, bacterial & fungal roulette,\u00a0 an ideal breeding ground for the proliferation of lifelong (inter-generational) viral, bacterial\u00a0& fungal (gut related) infections. <\/span><\/strong><\/div>\n
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The overwhelming body of scientific\u00a0evidence points to one\u00a0critical determining factor in the rise of mutagenic viruses & systemic erosion of natural immunity: multi-generational\u00a0community-w<\/span><\/strong>ide exposure to the Standard Immunization regime, in particular, those viral vaccines fixed on the schedule which combine multiple live attenuated viruses.\u00a0\u00a0\u00a0\u00a0<\/span><\/strong><\/div>\n
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\"Viral<\/a><\/div>\n
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‘<\/span><\/strong>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.<\/span><\/strong><\/a>‘ GIT Laboratory Journal<\/span><\/strong><\/p>\n

‘<\/span><\/b>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<\/span><\/b><\/span><\/a>.<\/a>‘ US National Institute of Allergy and Infectious Diseases <\/span><\/b><\/span><\/p>\n

‘<\/span><\/strong>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\u2019s ability to replicate at all is limited; however, it is taken into consideration when developing an attenuated vaccine. <\/span><\/strong><\/a><\/p>\n

It is worth noting that mutations are<\/em> 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).<\/strong><\/a>‘ College of Physicians, Philadelphia\u00a0<\/strong><\/span><\/p>\n

\u201c<\/span><\/strong>One vaccine decreases cell-mediated immunity by 50%, two vaccines by 70%\u2026all 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.<\/span><\/strong><\/a>\u201d\u00a0World-renowned Immunologist Dr. H.H. Fudenberg\u00a0<\/span><\/strong><\/p>\n

\"SWINE_468x286\"<\/a><\/p>\n<\/div>\n

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\u2018Adventitious agents (mutable viruses\/cross-contamination) could theoretically enter a viral vaccine through any of these ingredients (cell substrates, vaccine seed, tissue culture reagents, stabilizers).<\/a>\u2019 FDA\u00a0 <\/strong><\/p>\n

\u2018Many novel vaccines are produced in animal cell substrates, and emerging infectious diseases may theoretically be transmitted from animals to humans through these vaccines.<\/a>\u2019 FDA<\/strong><\/p>\n

\u2018Vaccines are increasingly becoming ineffective and causing \u201cimmune dysfunction. Additionally, \u201cvaccine antigen responses\u201d 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.<\/a>\u2019 Dr. Gary Null & Richard Gale\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 <\/strong><\/p>\n

\u2018There is concern that genetic technologies will be used to modify these already pathogenic agents and create \u201csuper-pathogens\u201d. 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.<\/a>\u2019 Impact of Synthetic Genomics on the Threat of Bioterrorism with Viral Agents, Marc S. Collett\/ViroDefense Inc.\u00a0 <\/strong><\/p>\n<\/div>\n

\"Animal<\/a>\u2018Many live attenuated vaccines for animals (including humans) are manufactured by using cell lines from animals, which are known to produce infectious \u2018<\/span><\/strong>endogenous retroviruses<\/span><\/strong><\/a>\u2018 (Remnants of ancestral exogenous retroviral infections fixed in the germline DNA); <\/span>however, the risks of infection by ERVs from xenospecies through vaccination have been ignored.<\/span><\/a>\u2019 Laboratory of Signal Transduction, Department of Cell Biology, Institute for Virus Research, Kyoto University<\/span><\/strong><\/div>\n

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‘<\/span><\/strong>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<\/span><\/strong><\/a>.’ Impact of Synthetic Genomics on the Threat of Bioterrorism with Viral Agents, Marc S. Collett\/ViroDefense Inc.<\/a><\/span><\/strong><\/p>\n

\"us-measles\"<\/a><\/p>\n

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 \u201cimmunized\u201d with the MMR series increases their risk of susceptibility to measles and transference of measles to other children in their proximity. <\/span><\/strong>As Dr Tetyana Obukhanych Ph.D, one of the world\u2019s leading Immunologists (guest speaker at our recent <\/span><\/strong>VRM Vaccine Summit<\/span><\/strong><\/a>) 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. <\/span><\/strong><\/div>\n

\"MMR<\/a>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\u2019s germ line DNA \u2013 manifesting in a more virulent strain of measles, known as \u2018Atypical Measles<\/a>‘) generated by the shot, passed on to the new generation.<\/span><\/strong><\/p>\n

The current generation have literally become unwitting hosts to a form of viral & bacterial roulette, <\/span><\/strong>an ideal breeding ground for the proliferation\/weaponizing of viral & bacterial infections<\/span><\/strong><\/a>.<\/span><\/strong><\/div>\n
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\u201cI am very concerned that \u201cimmunologic memory\u201d of adjuvant-containing vaccines is actually the basis of sensitization rather than the basis of immunity. Furthermore, I am very concerned that \u201csuccessful\u201d 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.<\/span><\/strong><\/p>\n

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\u2019s immunity. By doing so, vaccination campaigns wipe out population\u2019s 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.<\/span><\/strong><\/p>\n

All of this is a direct outcome of the \u201cdesired\u201d vaccination effects, the impact of which hasn\u2019t been carefully thought through in advance of introducing mass vaccination. We thought that vaccines work just like natural immunity. Well, apparently they don\u2019t and we are now reaping the consequences of that.<\/span><\/strong><\/p>\n

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. <\/span><\/strong><\/p>\n

I think this is happening because vaccination does not engage the genuine mechanism of immunity. Vaccination typically engages the immune response\u2014that is, everything that immunologists would theoretically \u201cwant\u201d 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.\u201d<\/span><\/strong> Dr Tetyana Obukhanych Ph.D<\/span><\/strong><\/a><\/p>\n

\u2018<\/span><\/strong>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.<\/span><\/strong><\/a><\/p>\n

The apparent paradox is that as measles immunization rates rise to high levels in a population, measles becomes a disease of immunized persons. Because of the failure rate of the vaccine and the unique transmissibility of the measles virus, the currently available measles vaccine, used in a single-dose strategy, is unlikely to completely eliminate measles. The long-term success of a two-dose strategy to eliminate measles remains to be determined.<\/span><\/strong><\/a>\u2018 Poland GA, Jacobson RM., Department of Internal Medicine, Mayo Vaccine Research Group, Mayo Clinic and Foundation, Rochester, MN.\/1994<\/span><\/strong><\/p>\n

\u2018<\/span><\/strong>As one of many examples involving all infectious diseases of childhood against which vaccines have been developed, ever since any measles vaccines have been introduced and used in mass proportions, reports of outbreaks and epidemics of measles in even 100% vaccinated populations started filling pages in medical journals. It is less well known to the general public that vaccinated children started developing an especially vicious form of measles, due to the altered host immune response caused by the deleterious effect of the measles vaccines. It resisted all orthodox treatment and carried a high mortality rate. It has become known as atypical measles (AMS).<\/span><\/strong><\/a><\/p>\n

In the meantime, outbreaks of measles in vaccinated children have continued and intensified to this day. Contemporary observations of the ineffectiveness of vaccination indicate to me that the incidence of measles has increased and has not continued decreasing as it did for some 100 years before any type of measles vaccination was introduced.<\/span><\/strong><\/a>‘ Dr Viera Scheibner (PhD), International Medical Counsel on Vaccination<\/span><\/strong><\/p>\n

\u2018<\/span><\/strong>We developed case criteria on the basis of serology and rash distribution and morphology. In typical measles a maculopapular rash occurs first at the hairline, progresses caudally, is concentrated on the face and trunk, and is often accompanied by Koplik\u2019s spots. In AMS the rash is morphologically a mixture of maculopapular, petechial, vesicular, and urticarial components. It usually begins and is concentrated primarily on the extremities, progresses cephalad, and is not accompanied by Koplik\u2019s spots. Cases were classified as AMS if patients had 1) a rash with the distribution and morphology characteristic of AMS, and 2) a fourfold or greater rise in titer of complement-fixing measles antibody or a convalescent titer of 256.<\/span><\/strong><\/a>\u2018 Dr. E M Nichols M.D.<\/span><\/strong><\/p>\n

Note: \u2018<\/strong>Measles-mumps-rubella (MMR) vaccines containing the Urabe strain of mumps were withdrawn in the United Kingdom in 1992 following demonstration of an increased risk of aseptic meningitis 15\u201335 days after vaccination.<\/span><\/strong><\/a>\u2026<\/strong>A total of 894 children (in the UK) were admitted to a hospital in the second year of life with febrile convulsion, or convulsion not otherwise specified, between January 1998 and June 2002 and had a linked MMR vaccination record. These children had a total of 988 convulsion episodes (819 had one episode, 60 had two, 12 had three, two had four, and one had five).<\/span><\/strong><\/a>\u2018 American Journal of Epidemiology\u00a0\u00a0\u00a0\u00a0 <\/strong><\/p>\n

The MMR Vaccine has co-infected an entire generation of children with a more virulent strain of Measles, now referred to as Atypical measles (AMS). The Medical Industry has reluctantly confirmed this vaccine-derived mutation circulating throughout the environment:<\/strong><\/p>\n

‘Atypical measles occurred (occurs) in children who received formalin-inactivated (killed) measles vaccine that was in use in the United States from 1963 to 1968. These children developed high fever, a rash that was most prominent on the extremities and often included petechiae, and a high rate of pneumonitis. Recent studies in monkeys indicate that this illness was caused by antigen-antibody immune complexes resulting from incomplete maturation of the antibody response to the vaccine.<\/a>‘ The Journal of Infectious Diseases <\/strong><\/p>\n

\u2018Atypical measles can occur in people who were immunized with a killed virus vaccine that was used from 1963-1967 and then exposed to the original virus. It can also occur in people who were immunized with the current vaccine but, for some reason, failed to develop immunity, and in people who are immunosuppressed.<\/a>‘<\/strong><\/p>\n

Note: \u2018The symptoms of atypical measles are different and more severe than the symptoms of typical measles.<\/a>‘<\/strong><\/p>\n

Symptoms of Vaccine-derived hybrid strain of Measles (Atypical Measles\/AMS):<\/strong><\/p>\n

1. Maculopapular ‘characterised by flat spots (macules) and tiny bumps (papules) on the surface of a tissue\u2014usually understood to mean the skin or an organ (e.g., the liver or spleen).’\u00a0\u00a0 <\/strong><\/p>\n

2. Petechial ‘pertaining to tiny red or purple spots caused by an extravasation of blood into the skin.’ <\/strong><\/p>\n

3. Vesicular ‘composed of or relating to small, saclike bodies.’ <\/strong><\/p>\n

4. Urticarial ‘hives; a vascular reaction of the upper dermis marked by transient appearance of slightly elevated patches (wheals) which are redder or paler than the surrounding skin and often attended by severe itching.’<\/strong><\/p>\n

‘<\/span><\/strong>Some vaccines, including the MMR, smallpox, and chickenpox vaccines, contain live viruses. By giving three and sometimes four live viruses together, the risk of developing a lifetime viral infection (a persistent viral infection) increases tremendously. This is especially so with the MMR vaccine, which contains two live viruses known to suppress the immune system for months.<\/span><\/strong><\/a>‘ Dr. Russell L. Blaylock M.D.\u00a0 <\/span><\/strong><\/p>\n

‘An outbreak of measles occurred in a high school with a documented vaccination level of 98 per cent. Nineteen (70 per cent) of the cases were students who had histories of measles vaccination at 12 months of age or older and are therefore considered vaccine failures…Vaccine failures among apparently adequately vaccinated individuals were sources of infection for at least 48 per cent of the cases in the outbreak.<\/a>‘ Measles outbreak in a vaccinated school population: epidemiology, chains of transmission and the role of vaccine failures –\u00a0American Journal of Public Health 05\/1987<\/strong><\/p>\n

Note: ‘Vaccine failures among apparently adequately vaccinated individuals were sources of infection for at least 48 per cent of the cases in the outbreak.’<\/strong><\/p>\n

‘Vaccination coverage for the total population was 99.0%. Incomplete vaccination coverage is not a valid explanation for the Quebec City measles outbreak.<\/a>‘ Major measles epidemic in the region of Quebec (1989) despite a 99% vaccine coverage – Boulianne N1, De Serres G, Duval B, Joly JR, Meyer F, D\u00e9ry P, Alary M, Le H\u00e9naff D, Th\u00e9riault N.\/PubMed 1991<\/strong><\/p>\n

‘The largest measles epidemic in North America in the last decade, occurred in 2011 in Quebec, Canada, where rates of 1- and 2-dose vaccine coverage among children 3 years of age were 95%-97% and 90%, respectively, with 3%-5% unvaccinated.<\/a>‘ Largest measles epidemic in North America in a decade–Quebec, Canada, 2011: contribution of susceptibility, serendipity, and superspreading events: De Serres G1, Markowski F, Toth E, Landry M, Auger D, Mercier M, B\u00e9langer P, Turmel B, Arruda H, Boulianne N, Ward BJ, Skowronski DM.\/PubMed <\/strong><\/p>\n

\"MMR<\/a>Dr. Andrew Wakefield\u2019s 1998 Study<\/span><\/a> demonstrated ‘anti-myelin antibodies (demyelination)\u00a0and digestive tract pathologies<\/a>‘ in children with autism after being given the Urabe strain triple live virus MMR vaccine. All 12 children in the Study had intestinal abnormalities (known as Inflammatory Bowel Disease), with chronic inflammation in the colon in 11 of the children. <\/span><\/strong><\/p>\n

Noted behavioral disorders included autism in 9, disintegrative psychosis in 1, and possible post-viral or vaccinal encephalitis (acute brain inflammation) in 2.<\/span><\/strong><\/p>\n

Since that release there have been countless other studies verifying exactly the same pattern \u2013 including the presence of measles lingering in the bowels of young children who have gotten of the Measles-Mumps-Rubella shot (MMR).<\/span><\/strong><\/p>\n

The Urabe strain MMR vaccine purchased by GlaxoSmitheKline for distribution in the UK, a triple live virus version, was directly responsible for an sudden spike in childhood Meningitis in the UK. It had been banned from use in Canada & was warned against further use in Britain by Canadian specialists. This was all suppressed by GSK & The British Gov\u2019t. They are solely to blame for this crisis.<\/span><\/strong><\/p>\n

‘<\/span><\/strong>‘The (UK) Government waited another two years before it decided to stop using Urabe MMR in 1992, after the manufacturers told officials that they would stop making it. It was replaced with MMR II, which has a different mumps component. <\/span><\/strong><\/a><\/p>\n

Prof Kent Woods, chief executive officer of the Medicines and Healthcare products Regulatory Agency, confirmed that the UK authorities had been aware of “sporadic cases” in Canada. However, the risk of meningoencephalitis from Urabe MMR was lower than the risk of the same condition resulting from “wild-type mumps virus”, he said.<\/span><\/strong><\/a><\/p>\n

Urabe MMR was withdrawn “following reports of generally mild transient meningitis caused by the mumps vaccine virus in some children who recently received the Urabe mumps vaccine containing products.<\/span><\/strong><\/a>‘ The Telegraph\/2007<\/span><\/strong><\/p>\n

\u2018<\/span><\/strong>The Urabe AM9 vaccine was developed in Japan and was originally attenuated by six passages of a wild isolate in chicken amniotic cavity, after which the virus underwent two plaque purifications in quail fibroblasts.<\/span><\/strong><\/a><\/p>\n

Specifically, the Urabe AM9 component of trivalent measles, mumps and rubella vaccines was associated with meningitis (inflammation of the meninges, the thin, membranous covering of the brain and the spinal cord)and parotitis (inflammation and infection of the salivary glands).<\/span><\/strong><\/a><\/p>\n

We also demonstrated that these same sequence differences, specifically a subset of mutations in the viral polymerase, control the ability of Gw7 and 1004-10\/2 to replicate in human cell lines<\/span><\/strong><\/a>.\u2019 Identification of Genetic Mutations Associated With Attenuation and Changes in Tropism of Urabe Mumps Virus\/Dion Shah, Silvia Vidal, Malen A. Link, Steven A. Rubin, and Kathryn E. Wright\u00a0\u00a0<\/span><\/strong><\/div>\n
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\"gsk-london\"<\/a><\/div>\n

\u201cI advocated very strongly for the use of the single vaccines, single Measles, Mumps, Rubella, which were available at the time in the UK. The vaccination uptake did not fall. MMR went down but there was a reciprocal increase in the use of single vaccines. Measles did not come back. Then, 6 months after I made that recommendation, the Gov\u2019t in the UK unilaterally withdrew importation license for the single vaccines; thereby depriving parents of an opportunity to vaccinate their children. THEN, vaccination rates went down, THEN measles came back. The British Gov\u2019t is solely responsible for that happening.<\/span><\/strong><\/p>\n

I have also found that regressive behavioral disorder (RBD) in children is associated with measles, mumps and rubella (MMR) vaccination. These children all have gastrointestinal symptoms including abdominal pain, diarrhea, and in some cases food intolerance. It is significant that this syndrome only appeared with the introduction of the polyvalent MMR vaccine in 1988 rather than with the monovalent measles vaccine introduced in 1968. This indicates that MMR is responsible for this condition rather than just the measles virus and that accordingly a transfer factor specific for the components other than the measles virus in MMR may be required.\u201d <\/span><\/strong>Dr. Andrew Wakefield <\/span><\/strong><\/a><\/p>\n

A\u00a0mutagenic Measles viral strain (<\/span>atypical measles<\/span><\/a><\/span>) commonly infects the bowels\/intestines of children with Autism, manifesting\u00a0as Inflammatory Bowel Disease – Intermediate\/Advanced Crohns & Colitis. Merck\u2019s official package insert for the Measles, Mumps, Rubella vaccine explains why: \u2018<\/span><\/strong>M-M-R II has not been evaluated for carcinogenic or mutagenic potential, or potential to impair fertility.<\/span><\/strong><\/a>\u2019<\/span><\/strong><\/p>\n

Measles, Mumps, Rubella Vaccine (series) \u2013 1st round given at 12-15 months old: \u2018<\/span><\/strong>The evidence convincingly supports a causal relationship between MMR vaccine and measles inclusion body enchephalitis (inflammation of the Brain & Meninges\/Meningoencephalitis manifesting as \u2018diffuse and\/or focal neuropsychological dysfunction<\/span><\/strong><\/a>\u2018<\/span><\/strong> \u2013 reaction to synergistic heavy metal-excipient accumulation of \u2019sludge\u2019 toxicity) in individuals with demonstrated immune deficiencies.\u2019 P.110 Institute of Medicine Report on Adverse Effects of Vaccines\/2011<\/span><\/strong><\/a><\/p>\n

Official Package Insert: \u2018<\/span><\/strong>M-M-R II is a sterile lyophilized preparation of (1) ATTENUVAX* (Measles Virus Vaccine Live), a more attenuated line of measles virus, derived from Enders\u2019 attenuated Edmonston strain and propagated in chick embryo cell culture; (2) MUMPSVAX* (Mumps Virus Vaccine Live), the Jeryl Lynn** (B level) strain of mumps virus propagated in chick embryo cell culture; and (3) MERUVAX* II (Rubella Virus Vaccine Live), the Wistar RA 27\/3 strain of live attenuated rubella virus propagated in WI-38 human diploid lung fibroblasts<\/span><\/strong><\/a>.\u2019<\/span><\/strong><\/p>\n

\"Giant<\/a>\u2018<\/span><\/strong>Measles\u00a0vaccine can cause problems (e.g. fatal giant cell pneumonia) in those\u00a0 with severely compromised cell-mediated immunity.<\/span><\/strong><\/a>\u00a0If a patient has an impaired cell-mediated immune response, there is\u00a0 continued growth of the virus in the lungs leading to giant cell\u00a0 pneumonia (such patients may not have a rash). This is rare, but often\u00a0 fatal.’ Dr. Margaret Hunt, University of South Carolina School of Medicine<\/span><\/strong><\/p>\n

‘<\/span><\/strong>The\u00a0development of giant cells has been illustrated in tissue cultures\u00a0 infected with adenoviruses and measles viruses, and in ferrets infected\u00a0 with distemper viruses.<\/span><\/strong><\/a>\u2018 Giant Cell Pneumonia: Clinicopathologic and\u00a0 Experimental Studies, J. M. Adams,, D. T. Imagawa,, Miye Yoshimori, R.\u00a0 W. Huntington<\/strong>\u00a0<\/span><\/p>\n

\"Measles_virus\"<\/a>‘One study, in which autopsied elderly were examined for the presence of the measles virus, found that<\/span><\/strong> 20% of the brains had live measles viruses and 45% of other organs were infected<\/span><\/strong><\/a>. These viruses were highly mutated, meaning that they could be just as potent as other measles viruses, but could be even more virulent. Worse, is that in most cases they cause a smoldering destruction of tissues without the obvious symptoms of infection, which has been shown in a number of studies.\u2019 Dr. Russell L. Blaylock M.D.<\/span><\/strong><\/p>\n<\/div>\n

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Government data admits to a probable causal link between vaccines & the (inexplicable) presence of <\/span><\/strong>Measles in the bowels<\/span><\/strong><\/a> of young children; while promoting a deliberate cover-up of these inherent risks to the general public,<\/span><\/strong><\/p>\n

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\u2018<\/span><\/strong>That Crohn\u2019s disease and other chronic inflammatory illnesses of the intestine might be caused by a virus such as measles is an interesting hypothesis.<\/span><\/strong><\/a> Until the present time, microbiologic and epidemiologic arguments either for or against this hypothesis have not been very convincing. It is not very likely that other epidemiologic studies will provide conclusive evidence. In fact, it would be difficult to find a population that includes both individuals who have been exposed to the virus or to the vaccine and individuals who have not been exposed. However, new microbiologic studies might prove conclusive.<\/span><\/strong><\/p>\n

First, it would be necessary to demonstrate that the measles virus is indeed present in the lesions, that it is active, and that it contributes to inflammatory responses. <\/span><\/strong>Also, it would be necessary to prove that the pathogenic reaction can be induced by the wild virus and by the attenuated viruses present in vaccines. Strains and attenuation procedures vary from one manufacturer to another, and it is far from certain that all strains have the same ability to persist in tissues and to subsequently produce chronic inflammations.<\/span><\/strong><\/a><\/p>\n

As was stated above, measles vaccine does not seem to be associated with SSPE (subacute sclerosing panencephalitis<\/a>), although the wild virus may be isolated (with difficulty) in patients with SSPE. The measles virus was isolated neither in patients with Crohn\u2019s disease or other chronic inflammatory diseases (Paget\u2019s disease, active chronic hepatitis, multiple sclerosis) in which a role for it has been claimed on morphologic, histologic or serologic grounds.<\/span><\/strong><\/p>\n

Current scientific data do not permit a causal link to be drawn between the measles virus and chronic inflammatory bowel diseases. 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.\u2019 Identification of Genetic Mutations Associated With Attenuation and Changes in Tropism of Urabe Mumps Virus, Journal of Medical Virology 81:130\u2013138\/2009\u00a0<\/span><\/strong><\/p>\n

Note:\u00a0 ‘\u2026it 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.’ <\/span><\/strong><\/div>\n<\/div>\n
\"Polio<\/a><\/div>\n<\/div>\n<\/div>\n
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Vaccinated individuals are highly susceptible to viral shedding for weeks, months, and often years following the inoculation procedure. Here is a recent Peer-reviewed analysis of an individual who received a dose of the Oral Polio Vaccine (OPV) in 1986, and has subsequently been virally shedding a mutated, more virulent (weaponized) strain of Polio for 28 years. <\/strong><\/p>\n

‘The latest isolate available was from 4th March 2015 showing a 17.7% VP1 sequence drift from Sabin 2 poliovirus. Phylogenetic analyses in the capsid region confirmed that the iVDPV strains were genetically related, sequentially evolved from Sabin 2 and distinct from other type 2 VDPVs and wild polioviruses\u00a0\u00a0<\/a><\/strong><\/p>\n

The date of the initiating OPV dose was estimated to be 11th March 1986 [HPD95 = 6th July 1983-11th January 1989], relatively close to 4th August 1986, the date of the patient\u2019s last known OPV vaccination. It is therefore most likely that this individual has been excreting (virally shedding a mutagenic\/chemically synthesized strain of) poliovirus for around 28 years.<\/strong><\/a><\/p>\n

Our results highlight the need for improving the standardisation of sIPV products in terms of measuring vaccine potency and defining the protective human dose.<\/a>‘ Twenty-Eight Years of Poliovirus Replication in an Immunodeficient Individual: Impact on the Global Polio Eradication Initiative – <\/strong>Dr.s Glynis Dunn, Dimitra Klapsa, Thomas Wilton, Lindsay Stone, Philip D. Minor, Javier Martin, National Institute for Biological Standards and Contol, Hertfordshire, Public Library of Science Pathogens\/August 27, 2015<\/strong><\/p>\n<\/div>\n

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\u00a0<\/span><\/div>\n
‘<\/span>Attenuated live vaccines also carry a potential risk of contamination with adventitious viruses introduced during the attenuation process, from the cell lines used, and\/or from the animal sera or other biologics often used in cell cultures. Very early Theiler’s yellow fever attenuated virus was once \u201cstabilized\u201d with human plasma thought to contain hepatitis B virus, resulting in many cases of hepatitis. Some early Sabin poliovirus vaccines were contaminated with the simian virus 40 (SV40) polyomavirus from the monkey cells used to amplify polioviruses.<\/span><\/a><\/strong><\/div>\n
\u00a0<\/span><\/div>\n
Metagenomics and a panmicrobial microarray were used to examine eight live-attenuated viral vaccines. Viral nucleic acids in trivalent oral poliovirus (OPV), rubella, measles, yellow fever, varicella-zoster, multivalent measles\/mumps\/rubella, and two rotavirus live vaccines were partially purified, randomly amplified, and pyrosequenced. Over half a million sequence reads were generated covering from 20 to 99% of the attenuated viral genomes at depths reaching up to 8,000 reads per nucleotides. <\/span><\/a><\/span><\/strong><\/div>\n
\u00a0<\/span><\/a><\/div>\n
Mutations and minority variants, relative to vaccine strains, not known to affect attenuation were detected in OPV, mumps virus, and varicella-zoster virus. The anticipated detection of endogenous retroviral sequences from the producer avian and primate cells was confirmed. Avian leukosis virus (ALV), previously shown to be noninfectious for humans, was present as RNA in viral particles, while simian retrovirus (SRV) was present as genetically defective DNA<\/span>.<\/span><\/a>\u2019<\/span> Journal of Virology, June 2010 vol. 84 no. 12 <\/span><\/strong><\/div>\n
\u00a0<\/span><\/div>\n
Note:\u00a0The\u00a0impact\/presence\u00a0of\u00a0‘<\/span>adventitious\u00a0agents<\/a><\/span><\/span>‘\u00a0&\u00a0‘genetically defective DNA<\/span><\/a>‘\u00a0renders\u00a0a baby\/infant\u00a0highly susceptible to (otherwise avoidable) hybrid forms of early childhood cancer, including that of emerging infectious diseases<\/a>. \u00a0<\/span><\/strong><\/div>\n
\u00a0<\/span><\/strong><\/div>\n
‘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). <\/span><\/strong>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<\/span><\/strong>\u2026the degree of attenuation of laboratory-passaged viruses may or may not be known. There can in some cases be uncertainty regarding the biological attributes of a synthetic replica of a gene bank virus sequence.<\/span><\/a>‘ Impact of Synthetic Genomics on the Threat of Bioterrorism with Viral Agents <\/strong><\/span><\/div>\n
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\"Designer<\/a><\/div>\n
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Note: Vaccine Manufacturers routinely & deliberately bury\/gloss over\u00a0negative Clinical Trial data, in their endless pursuit of higher profits,\u00a0reinforced\u00a0by Government Health Departments & Mainstream Media outlets. Given such clear discrepancies & wanton disregard for honest\/accurate reporting, without any genuine accountability, the ultimate burden of responsibility shifts to\u00a0families, through education & avoidance of\u00a0these hidden\u00a0landmines. Knowledge\u00a0equates\u00a0freedom. <\/span><\/strong><\/strong><\/p>\n

<\/div>\n<\/div>\n
‘<\/span>Extensive evidence of reporting bias of safety outcomes from trials of live attenuated influenza vaccines (LAIVs) impeded meaningful analysis. One specific brand of monovalent pandemic vaccine is associated with cataplexy and narcolepsy in children and there is sparse evidence of serious harms (such as febrile convulsions) in specific situations.<\/span><\/a><\/span>\u2019 <\/span>Jefferson T, Rivetti A, Di Pietrantonj C, Demicheli V, Ferroni E, published in Cochrane Library\/<\/span><\/strong><\/strong><\/strong>2012<\/span><\/strong><\/strong><\/div>\n
\"LEIDEN<\/a><\/div>\n

In many ways the greatest threat posed by\u00a0modern Vaccine Technology is the advent of cloning, in & of itself; the hubris of replicating\/mass-producing, from scratch, signature protein epitopes (ie. to construct an ‘<\/span><\/strong>innovative synthetic influenza vaccine<\/span><\/strong><\/a>‘). As always, nature will inevitably prove itself resilient to change, and will respond to man\u2019s attempts at reshuffling the deck by (forcibly) re-assorting the species.\u00a0<\/strong><\/span><\/p>\n

We have opened another Pandora\u2019s Box here, and with it, the clear probability\u00a0of “unforeseen” genetic mutations, for generations to come\u00a0\u2013 given the inexactitude and reckless disregard for the long-term consequences of this brand of (Frankenstein) science; a dangerous game of genetic roulette<\/span><\/a>, in\u00a0which our communities at large\u00a0have become unwitting volunteers in the greatest experiment since the advent of the Industrial Age. <\/strong><\/span><\/p>\n

The common trend? The rise of mutagenic viral transference & hybrid forms of Cancer impacting on\u00a0successive generations. <\/strong><\/span><\/p>\n

‘Advances in synthetic biology are allowing researchers to overcome these barriers in live attenuated vaccine development. It is now possible to order large segments of synthetic DNA, assemble them into entire genomes of infectious agents, and boot them to life – as was first published by Eckard Wimmer and colleagues with poliovirus in 2002, and has recently been applied to Mycoplasmamycoides in Craig Venter’s lab. The ability to create viable viruses by chemical synthesis based solely on sequence design allows us to rapidly modify large segments of the viral genome without altering the amino acid sequence, leading to controlled and deliberate attenuation of the virus.<\/a>‘\u00a0GIT Laboratory Journal<\/strong><\/div>\n
<\/div>\n
\"Transhumanism\"<\/a><\/div>\n
<\/div>\n
The only realistic solution to this manufactured crisis is a community-wide reinvesting in holistic thinking & the legitimate science of the body. The Vaccine Industry relies solely on so-called \u201cEmpirical\u201d (Absolute) Science to justify implementing herd immunity-type policies. However, the whole foundation on which symptom-based Allopathic Medicine is built runs counter to the holistic principles of the human body.<\/strong><\/a><\/div>\n
<\/div>\n
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\"Immune-Function\"We have been socially engineered by a blind-sighted Technocracy, deceived into believing all the lies put forth by Western Allopathic Medicine, the whole mistaken ideology & foundation surrounding Immunization as a practice; an antithetical approach which runs counter to nature, that of COMBATING or shielding yourself off from the environment by artificially shocking or jump-starting the body into recognizing external \u201cthreats\u201d, rather than holistically EMBRACING all that we come in contact with, thereby re-enforcing, through HARMONY, the inherent properties of natural immunity.<\/a><\/strong><\/p>\n

Viruses thrive in a non-alkaline, heavily acidic environment. The human body needs to maintain a pH (parts Hydrogen) ratio of between 6.8 and 7.1 (Alkalinity) to that of Acidity (between 2.9 and 3.2\/10), in order to sustain a healthy internal balance. Apple Cider Vinegar (strictly organic) provides the body with an ideal quotient. It is recommended you take a swig of ACV (diluted) 2-3 days per week (routine may vary according to your constitution), at the start of each day. Sodium Bi-carbonate\/Organic baking soda (teaspoon diluted in water) should also be taken at the end of each day (alternately added to your bath). This gives your body a powerful \u201cdouble punch\u201d impact\/velocity against the onset of infections & long-term cancer.<\/strong><\/a><\/p>\n

Cancer cells thrive in an oxygen-deprived environment. Within 72 hours of oxygen deprivation any cell will become cancerous. This will occur when vaccine derived bio-conductive aluminum (consisting of live virus, antibiotic, heavy metal, detergent coagulated sludge) clogs the vast network of arterial veins & capillaries, inducing Ischemia.<\/strong><\/a><\/p>\n

Consider these options. The road back to optimal health is ultimately in your hands. Our children are counting on us to steer the course toward a brighter & healthier future. It is up to you.<\/strong><\/a><\/p>\n<\/div>\n<\/div>\n<\/div>\n

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\"VRM5\"<\/a><\/div>\n
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\u2018<\/span>If vaccinated children and adults are capable of spreading disease, shall we hold them and their parents legally liable for outbreaks? Shall we mandate \u2018unvaccination\u2019 as a requirement for public school? Since we can\u2019t \u2018unvaccinate,\u2019 shall vaccinated children be kicked out of public school?<\/span><\/a>\u2018 Toni Bark M.D.\u00a0<\/span><\/strong><\/strong><\/strong><\/div>\n
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\"vaccine_resistance_movement\"<\/a>The Vaccine Resistance Movement is currently launching its first ever educational DVD, the \u2018Silent No More Project<\/a>\u2018: where-in parents of vaccine-injured children reveal intimate details of the impact vaccines had on their child\u2019s primary early development. This ground-breaking event marked the first big push forward following the recent, highly controversial \u2018VRM Vaccine Summit\u2019. <\/strong><\/div>\n
<\/div>\n
\"Silent<\/a><\/div>\n
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VRM: The Autism Report http:\/\/vaccineresistancemovement.org\/?p=10185<\/a><\/strong><\/p>\n

VRM: Worldwide Autism Study Direct link to study: http:\/\/study.vaccineresistancemovement.org\/<\/a><\/strong><\/p>\n

VRM: The Problem With Vaccines Part 1 http:\/\/vaccineresistancemovement.org\/?p=488<\/a><\/strong><\/p>\n

VRM: Vaccine Clinic \u2013 A Concise Compendium To The Problem With Vaccines<\/strong> http:\/\/vaccineresistancemovement.org\/?p=6278<\/a><\/strong><\/p>\n

VRM: The Problem With Vaccines Part 2 \u2013 Synergistic Effect of Heavy Metal Toxicity On The Body http:\/\/vaccineresistancemovement.org\/?p=6097<\/a><\/strong><\/p>\n

VRM: The Problem With Vaccines Part 3 \u2013 Synthetic Genomics & The Death Of Natural Immunity http:\/\/vaccineresistancemovement.org\/?p=6880<\/a><\/strong><\/p>\n

VRM: A Concise Compendium To The Problem With Vaccines Part 3 \u2013 Synthetic Genomics & The Death Of Natural Immunity http:\/\/vaccineresistancemovement.org\/?p=7283<\/a><\/strong><\/p>\n

VRM: The Problem With Vaccines Part 4 \u2013 Primary Aspects of Vaccine Toxicity Affecting Body http:\/\/vaccineresistancemovement.org\/?p=8787<\/a><\/strong><\/p>\n

VRM: The Problem With Vaccines Part 5A \u2013 Detoxification & Restoration of the Body http:\/\/vaccineresistancemovement.org\/?p=8836<\/a><\/strong><\/p>\n

VRM: The Problem With Vaccines Part 5B \u2013 Detoxification & Restoration of the Body http:\/\/vaccineresistancemovement.org\/?p=8847<\/a><\/strong><\/p>\n

VRM: PCV Vaccine Exposed \u2013 Breeding Ground For Staphylococcus Aureus http:\/\/vaccineresistancemovement.org\/?p=9431<\/a><\/strong><\/p>\n

VRM: Pandemic Preparedness & The Dark Agenda Ahead http:\/\/vaccineresistancemovement.org\/?p=9460<\/a><\/strong><\/p>\n

VRM: Mandatory Vaccinatio\u200bns \u2013 How They Will Be Implemente\u200bd http:\/\/vaccineresistancemovement.org\/?p=11806<\/a><\/strong><\/p>\n

VRM: The Confidenti\u200bal Case-files of GlaxoSmith\u200bKline \u2013 Cover-up, Deferral & Denial of Responsibi\u200blity for Vaccine-re\u200blated Premature Deaths http:\/\/vaccineresistancemovement.org\/?p=12242<\/a><\/strong><\/p>\n

VRM: Polio \u2013 United Nations & The Great Cull http:\/\/vaccineresistancemovement.org\/?p=4916<\/a><\/strong><\/p>\n

VRM: The Re-emergence of Polio in The Third World (compliments of the World Health Organization & Bill Gates) http:\/\/vaccineresistancemovement.org\/?p=10091<\/a><\/strong><\/p>\n

VRM: Weaponized Polio & The African Green Monkey Conundrum <\/strong> http:\/\/vaccineresistancemovement.org\/?p=10727<\/a><\/strong><\/p>\n

VRM: Primary Reasons Not To Get The Flu Shot http:\/\/vaccineresistancemovement.org\/?p=12642<\/a><\/strong><\/p>\n

VRM: The Flu Report http:\/\/vaccineresistancemovement.org\/?p=9226<\/a><\/strong><\/p>\n

VRM: Vaccine Ingredients http:\/\/vaccineresistancemovement.org\/?p=979<\/a><\/strong><\/p>\n

VRM: Safe Alternatives to Vaccines<\/strong> http:\/\/vaccineresistancemovement.org\/?p=662%EF%BB%BF<\/a><\/strong><\/p>\n

VRM: Family Charts Gradual Decline Of Daughter http:\/\/vaccineresistancemovement.org\/?p=3156<\/a><\/strong><\/p>\n

VRM: Health Matters Part 1 http:\/\/vaccineresistancemovement.org\/?p=6719<\/a><\/strong><\/p>\n

VRM: Health Matters Part 2<\/strong> http:\/\/vaccineresistancemovement.org\/?p=6746%EF%BB%BF<\/a><\/strong><\/p>\n

VRM: Alternative Cancer Cures That Work http:\/\/vaccineresistancemovement.org\/?p=3729<\/a><\/strong><\/p>\n

VRM: Pregnancy Tips<\/strong> http:\/\/vaccineresistancemovement.org\/?p=3270<\/a> <\/strong><\/p>\n

VRM: H1N1 Shot Reactions \u2013 Miscarriages http:\/\/vaccineresistancemovement.org\/?p=943<\/a><\/strong><\/p>\n

VRM: The Vanishing Sperm Count http:\/\/vaccineresistancemovement.org\/?p=4639<\/a><\/strong><\/p>\n

VRM: H1N1 Vaccine Surplus From 2009 Reveals Growing Distrust of Gov\u2019t & WHO http:\/\/vaccineresistancemovement.org\/?p=4969<\/a><\/strong><\/p>\n

VRM: Flu Death Statistics \u2013 WHO & The Big Lie http:\/\/vaccineresistancemovement.org\/?p=784<\/a><\/strong><\/p>\n

VRM: Vaccine Industry Deception, Propaganda & Media Collusion<\/strong> http:\/\/vaccineresistancemovement.org\/?p=197<\/a><\/strong><\/p>\n

VRM: Birth of Medical & Scientific Dictatorship \u2013 Future Scenarios http:\/\/vaccineresistancemovement.org\/?p=997<\/a><\/strong><\/p>\n

VRM: H1N1 Bio-weaponry Incorporated http:\/\/vaccineresistancemovement.org\/?p=884<\/a><\/strong><\/p>\n

VRM: Aids & The WHO Connection \u2013 Criminal Intent<\/strong> http:\/\/vaccineresistancemovement.org\/?p=1749<\/a><\/strong><\/p>\n

VRM: Morgellons Syndrome & Chemtrails http:\/\/vaccineresistancemovement.org\/?p=839<\/a><\/strong><\/p>\n

VRM: Council On Foreign Relations 10\/16\/09- Major Influence on Government Vaccine Policy<\/strong> http:\/\/vaccineresistancemovement.org\/?p=1880<\/a><\/strong><\/p>\n

VRM: Closed Door CDC Meeting Reveals Industry Cover-up Of Heavy Metal Toxicity In Vaccines http:\/\/vaccineresistancemovement.org\/?p=5935<\/a><\/strong><\/p>\n

VRM: The Rockefeller Foundation Drafts A Post-Pandemic Scenario http:\/\/vaccineresistancemovement.org\/?p=5102<\/a><\/strong><\/p>\n

VRM: World Health Organization & Vaccine Manufacturers\u00a0\u00a0\u00a0 Implicated In Massive H1N1 Financial Scam Involving Kickbacks &\u00a0\u00a0\u00a0 Cover-ups<\/strong> http:\/\/vaccineresistancemovement.org\/?p=4610<\/a><\/strong><\/p>\n

VRM Live \u2013 01\/28\/11: Vaccine Resistance Movement founder Joel\u00a0\u00a0\u00a0 Lord\u00a0 discusses Synthetic Genomics, cloned cell vaccine technology\u00a0\u00a0\u00a0 & the\u00a0 death of natural immunity, gutter journalism & Dr.\u00a0\u00a0\u00a0 Wakefield\u2019s\u00a0 imminent vindication with \u2018Truth to Power\u2019 host Paul\u00a0\u00a0\u00a0 Mabelis. http:\/\/www.blogtalkradio.com\/empradio\/2011\/01\/28\/truth-to-power-thursday<\/a><\/strong><\/p>\n

VRM Live <\/strong>– 11\/04\/10<\/strong>: <\/strong>Vaccine\u00a0\u00a0\u00a0\u00a0 Resistance Movement founder Joel Lord lays out the whole vaccine\u00a0\u00a0\u00a0 process\u00a0 with Paul Mabelis; including heavy metal toxicity, synergy,\u00a0\u00a0\u00a0\u00a0 pregnancy issues & the basic principles of natural health at risk. http:\/\/www.blogtalkradio.com\/show.aspx?userurl=empradio&year=2010&month=11&day=05&url=truth-to-power-thursday<\/a><\/strong><\/p>\n

VRM Live <\/strong>– 09\/24\/10<\/strong>:\u00a0\u00a0\u00a0 Vaccine\u00a0 Resistance Movement Founder Joel Lord & activist\/radio\u00a0\u00a0\u00a0 host Jesse\u00a0 Calhoun lay it all out tonite. Topics include the VRM\u00a0\u00a0\u00a0 Worldwide Autism Study, <\/strong>Scientific\/Medical\u00a0 dictatorship, Natural Rights & Vaccine Industry fraud exposed. Special thanks to host Paul Mabelis. http:\/\/www.blogtalkradio.com\/empradio\/2010\/09\/24\/truth-to-power-thursday<\/a><\/strong><\/p>\n

If you appreciate the efforts to bring this information\u00a0\u00a0 forward\u00a0 do consider making a donation. Any amount, no matter how small\u00a0\u00a0 will\u00a0 help enable me to carry on this invaluable research. See Paypal\u00a0\u00a0 link\u00a0 on the VRM website <\/strong>(click on \u2018Donate\u2019 tab in upper right corner)<\/strong><\/strong><\/strong><\/strong><\/strong>. Thank you all.<\/strong><\/p>\n

\"logo.VRM_Ver.2.1\"<\/a><\/p>\n<\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"

  According to the vanguard\u00a0of the Vaccine Industry,\u00a0‘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\u00a0(where-in the viral component is purportedly “killed”\u00a0via chemical\/heat-treatment or exposure to gamma-rays), live attenuated vaccines have the benefit of a more efficient […]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[226],"tags":[],"class_list":["post-13124","post","type-post","status-publish","format-standard","hentry","category-vrm-the-rise-of-mutagenic-viruses"],"_links":{"self":[{"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=\/wp\/v2\/posts\/13124","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=13124"}],"version-history":[{"count":84,"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=\/wp\/v2\/posts\/13124\/revisions"}],"predecessor-version":[{"id":14820,"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=\/wp\/v2\/posts\/13124\/revisions\/14820"}],"wp:attachment":[{"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=13124"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=13124"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=13124"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}