VRM: Weaponized Polio & The African Green Monkey Conundrum

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.

 

‘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.

 

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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