VRM: Weaponized Polio & The African Green Monkey Conundrum

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20th September 2012 – By Joel Lord

According to a ground-breaking, controversial report, released in 1961 in the wake of the Salk & Sabin Polio vaccine debacle, Medical researchers identified that ‘all primary monkey kidney may contain one or more latent viruses whose characteristic cytopathology becomes evident when such tissue is cultured in uitro (in a Petri dish).‘…

‘It is now becoming apparent that all primary monkey kidney (source of ALL Polio vaccine strains & Oral drop versions) may contain one or more latent viruses (source of Endogenous retroviruses – remnants of ancestral exogenous retroviral infections fixed in the germline DNA) whose characteristic cytopathology (cell degeneration/disease) becomes evident when such tissue is cultured in uitro (chemically synthesized in a laboratory rather than within a living organism or natural setting).‘ L. Hayflick & P. S. Moorhead, Wistar Institute of Anatomy & Biology, Philadelphia, Pa., U.S.A., May 15, 1961

– meaning that not only was the DISEASED African Green Monkey (initially Rhesus Monkey derived) kidney tissue culture (in which the original Poliomavirus strains 1, 2 & 3 were nurtured) at fault, but also those kidneys subsequently extracted from HEALTHY African Green Monkeys; essential in the development & manufacturing of ALL Polio vaccines/drops circulated worldwide since 1962, integrated into the Standard Immunization regime here in the West and circulated throughout the Third World via United Nations’ directed Mass Vaccination Programs.

Note: ‘Serious objections, however, may be raised even to the use of this tissue. It is well known that primary monkey kidney has a very high content of latent simian viruses. Indeed, at least 18 such viruses have now been isolated from primary monkey kidney. One of these latent viruses (B virus) is even known to have caused fatalities in man.‘ – Reference Page 617

The obvious culprit here, the elephant in the room, which most so called “expert” observers have seemingly overlooked (more likely ignored)? Latent inter-generational Simian Virus (SV40) cross-contamination, from infected monkeys, now embedded in the African Green Monkey & Rhesus COLONIES (through monkey to monkey viral shedding), lingering in the DNA gene pool well after 1962/63; compounded by the ongoing laboratory synthesis of the primary Salk Vaccine version (SV40 contaminated) Rhesus seed strain.

Patent on African green monkey kidney cell lines useful for maintaining viruses and for preparation of viral vaccines: ‘The invention relates to a novel African Green Monkey Kidney (AGMK) cell subtrate that supports the efficient replication of human and animal rotaviruses, astroviruses, enteroviruses including the Sabin live attenuated poliovirus vaccine strains, hepatitis A virus and respiratory viruses such as respiratory syncytial virus, parainfluenza viruses, and influenza A and B viruses.’

‘Xenotropic murine leukemia (cancer) virus-related virus (XMRV) is a recently discovered human (endogenous, cloned) retrovirus that has been found in both chronic fatigue syndrome (Fibromyalgia) & prostate cancer patients. Although these findings need further confirmation, there is a potential safety concern regarding XMRV in cell substrates used in vaccines and in transmission by blood transfusion and blood products.’ FDA

‘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

‘On March 25, 1961, the federal regulations that controlled the production of oral poliovirus vaccine were amended. These new regulations did not require the vaccine manufacturers to discard their SV40-contaminated poliovirus seeds which were the source for all subsequent polio vaccines. Instead, the rules required that “each seed virus used in manufacture shall be demonstrated to be free of extraneous microbial agents.” The new regulations also required that each pair of monkey kidneys removed from a monkey for vaccine production “shall be examined microscopically for evidence of cell degeneration.” Furthermore, fluid from the monkey kidney cells had to be combined with other tissue cultures in order to detect if there was any contaminating virus. The regulations required that “the cultures shall be observed for at least 14 days.”‘ Michael E. Horwin M.A, J.D.

‘Although manufacturers switched from rhesus monkeys to SV40-free green African monkeys to grow the bulk vaccine in 1961, they have continued to use potentially contaminated polio seed strains originally grown on the rhesus monkey (kidney)tissue to start the bulk vaccine process. Manufacturers check the purity of their vaccine with a series of 14-day tests to detect whether any SV40 slipped through. But when Carbone (SV40 virus researcher Dr. Michele Carbone) replicated the tests, he found that the second, slower growing ‘archetypal’ strain took 19 days to emerge. Carbone noted in a published report that it is possible that this second strain of SV40 had been evading manufacturers’ screening procedures for years — and continued to infect vaccine recipients after 1962.

By the end of 1996, dozens of scientists reported finding SV40 in a variety of bone cancers and a wide range of brain cancers, which had risen 30 percent over the previous 20 years. Then, Italian researchers reported finding SV40 in 45 percent of the seminal fluid samples and 23 percent of the blood samples they had taken from healthy donors. This meant that SV40 was probably spreading through sexual activity, transmitted from mother to child, raising the possibility that the virus may now be incorporated into our genetic makeup. Another possibility is that, undetected by vaccine manufacturers, the virus continues to contaminate current stocks of polio vaccine.” William Carlsen, SFGate Chronicle, 07/15’2001

‘Michele Carbone of Loyola University Medical Center in Chicago has announced results that suggest the Soviet polio vaccine was contaminated after 1963, possibly until the early 1980s. “Is there infectious virus? The short answer is, yes,”. The vaccine was almost certainly used throughout the Soviet bloc and probably exported to China, Japan and several countries in Africa. That means hundreds of millions could have been exposed to SV40 after 1963… He has confirmed the presence of SV40 in the Soviet vaccine samples using three separate tests. In two of the samples, he also showed that the SV40 remained infectious.‘

This indicates that either Simian variant (substrate) of African Green Monkey & Rhesus Monkey type kidney tissue culture, whether diseased (transformed/malignant) or determined as healthy (benign), when combined with the Poliomavirus strains in a vaccine and injected subcutaneously or intramuscularly into the blood stream, produces the conditions for a breeding ground of degeneration in the human body, rapidly/gradually manifesting as hybrid forms of cancer, particularly brain, bone and lung-related tumors, childhood Leukemia…”directly responsible for the major increase in leukemia in this country.”, including a range of Coxsackie-type viruses such as Post-Polio Syndrome, Chronic Fatigue Syndrome or Myalgic Encephalomyelitis & Aseptic Meningitis.

“Many here voice a silent view that the Salk and Sabin vaccine (source of original Polio vaccine launched in 1954), being made of monkey tissue (grown in diseased African Green Monkey & Rhesus Monkey kidney tissue culture)…has been directly responsible for the major increase in leukemia (hybrid cancer) in this country (US).” Frederick Klenner M.D.

‘More than 98 million Americans received one or more doses of polio vaccine from 1955 to 1963 when a proportion of vaccine was contaminated with SV40; it has been estimated that 10–30 million Americans could have received an SV40 contaminated dose of vaccine.’ CDC’s now infamous statement, which was promptly removed from their official website, then promptly removed from Google’s cached page records

‘Simian virus 40 (SV40) sequences have recently been identified in a variety of human neoplasms, including mesothelioma, osteosarcoma, and brain tumors, but significant discrepancies exist regarding the frequency at which this occurs. The SV40 genome is 70% homologous to JC and BK, two related polyomaviruses that are highly prevalent in humans and which may cause in immune-compromised patients progressive multifocal leukoencephalopathy (PML) and cystitis, respectively.‘ Identification in human brain tumors of DNA sequences specific for SV40 large T antigen, Brain Pathology/1999 Jan;9(1):33-42.

The WHO and all their Corporate Mainstream Media minions pushing Vaccine propaganda on the public, have, in fact, betrayed our communities, betrayed the Third World, and literally re-invigorated Polio, having spawned a new, virulent hybrid of Polio, known as ‘Non-Polio Acute Flaccid Paralysis (NPAFP), throughout the Third World via cross-infection & viral shedding, stemming from the original SV40 tainted Salk Polio (Rhesus monkey colony derived) vaccine formula & subsequent African Green Monkey Kidney source utilized in the follow-up Sabin formula (including the sugar cube version), further contaminated with the primary Simian Virus/SV40 seed strain; reconstituted via chemical synthesis to produce the current model, now being forced on children throughout the Third World (otherwise symptom-free from Polio), a live monovalent Oral Polio Type 1 Vaccine (mOPV Type 1), which contains suspension of live attenuated poliomyelitis type 1 virus (Sabin strain) prepared in Monkey Kidney cells – which is now being forced on millions of children, otherwise symptom-free from Polio. ‘Government of India and its 2.3 million vaccinators visited over 200 million households to ensure that the nearly 170 million children (under five years in age) were repeatedly immunised with oral polio vaccine (OPV)‘‘

‘After the global eradication of wild polioviruses, the risk of paralytic poliomyelitis from polioviruses will still exist and require active management. Possible reintroductions of poliovirus that can spread rapidly in unprotected populations present challenges to policymakers. For example, at least one outbreak will likely occur due to circulation of a neurovirulent vaccine-derived poliovirus after discontinuation of oral poliovirus vaccine and also could possibly result from the escape of poliovirus from a laboratory or vaccine production facility or from an intentional act.

In addition, continued vaccination with oral poliovirus vaccines would result in the continued occurrence of vaccine-associated paralytic poliomyelitis. The likelihood and impacts of reintroductions in the form of poliomyelitis outbreaks depend on the policy decisions and on the size and characteristics of the vulnerable population, which change over time. A plan for managing these risks must begin with an attempt to characterize and quantify them as a function of time.’ Risks of paralytic disease due to wild or vaccine-derived poliovirus after eradication – Radboud J Duintjer Tebbens, Mark A Pallansch, Olen M Kew, Victor M Cáceres, Hamid Jafari, Stephen L Cochi, Roland W Sutter, R Bruce Aylward, Kimberly M Thompson (Kids Risk Project), Harvard School of Public Health, Boston, MA, USA. 2006

During 2011, incidence of Non-Polio Acute Flaccid Paralysis (clinically indistinguishable from polio paralysis but twice as deadly…incidence of NPAFP was directly proportional to doses of oral polio received) in India, alone, skyrocketed to 60,754 cases; coinciding with the culmination of the most intense, widespread phase ever conducted in India’s Oral Polio Vaccination “reaching every child” campaign. While meanwhile the WHO have conveniently removed India from the list of Polio endemic countries; because they’re not looking for a Polio hybrid in the first place.

The World Health Organization (WHO) have deliberately focused merely on identifying cases of the standard Wild Polio Virus/WPV strain (Types 1, 2 & 3) – itself the by-product of diseased African Green Monkey Kidney/Rhesus (Simian Virus 40/SV40) inter-generational cross-contamination from the original Salk Polio Vaccine (1955); while failing to acknowledge that, in fact, their recommended live monovalent Oral Polio Type 1 Vaccine (mOPV Type 1), which contains suspension of live attenuated poliomyelitis type 1 virus (Sabin strain) prepared in Monkey Kidney cells, has spawned a new, virulent hybrid of Polio, known as ‘Non-Polio Acute Flaccid Paralysis (NPAFP), throughout the Third World; including cross border transference of Non-Polio Acute Flaccid Paralysis type Polio through inevitable post-immunization community wide viral shedding.

‘Polio refers to all polio cases (indigenous or imported), including polio cases caused by vaccine derived polio viruses (VDPV); it does not include cases of vaccine-associated paralytic polio (VAPP) and cases of non polio acute flaccid paralysis [AFP]).‘ WHO

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