VRM: Weaponized Polio & The African Green Monkey Conundrum

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VRM: Weaponized Polio & The African Green Monkey Conundrum

VRM: Weaponized Polio & The African Green Monkey Conundrum

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

Note: The same cross-contamination, hybrid (laboratory produced, synthetic) Polio strain now manifesting throughout the Third World as Non-Polio Acute Flaccid Paralysis, will concurrently be passed on, generation to generation, throughout impoverished areas, embedded in the baby’s genetic DNA material, via the Placenta & Colostrum; a predictable pattern which also holds true throughout the West, given the widespread exposure to tainted Polio Vaccine vials leading up to and afer 1962/63. An Industry cover-up of this magnitude requires blanket denial from not only the WHO, CDC & NIH, but also the cooperation of all Mainstream Media channels and nationally directed Health Departments, in order to sweep the entire mess under the carpet, thereby avoiding a runaway scandal which could ultimately bring down the entire apparatus.

As pointed out in VRM: The Re-emergence of Polio in The Third World (compliments of the World Health Organization & Bill Gates), Polio has become the Vaccine Industry’s flagship model of so called progress, and an argument perpetually used in favor of imposing vaccine uptake on the general population. The Western Medical Establishment & those who still trust in that system for answers, always look to their having “conquered” Polio as a benchmark justifying Herd Immunity type Immunization, in terms of succeeding where nature, left to its own devices, would have inevitably failed us.

Another troubling aspect to this vicious cycle which most Western observers sitting comfortably away from this mess don’t seem to grasp at the heart of it all – the inevitable snow-ball effect of Viral shedding & cross border (particularly international) movement to & from these epicenters, which is going to ensure that weaponized Polio once again “washes up on our shores”. However this time it’s impact will be far greater, due to decades of laboratory synthesis of the wild Polio strain. It’s going to be 1950 all over again.

‘An extremely rare, polio-like disease has appeared in more than a dozen California children within the past year, and each of them suffered paralysis to one or more arms or legs, Stanford University researchers say. But public health officials haven’t identified any common causes connecting the cases.

The illness is still being investigated and appears to be very unusual, but Dr. Keith Van Haren at Lucile Packard Children’s Hospital at Stanford University warned Monday that any child showing a sudden onset of weakness in their limbs or symptoms of paralysis should be immediately seen by a doctor. “The disease resembles but is not the same as polio,” he said. “But this is serious. Most of the children we’ve seen so far have not recovered use of their arm or their leg.”‘ California/Feb 24, 2014

‘In the cases, he said, children experience a “sudden onset of flaccid weakness that can occur over the course of hours,” affecting one or more limbs. All five children had been vaccinated against the poliovirus. Treatment did not seem to help the children regain their motor function.

Samples from two of those children tested positive for enterovirus 68, a rare virus that has been linked to severe respiratory illness in the past. Samples from the other three children were not collected or tested soon enough to yield conclusive results, said Dr. Emmanuelle Waubant, a neurologist at the University of California, San Francisco. “About 20 cases have been identified in the U.S. so far, all in California, and all occurring in the past 18 months. The prognosis that we’ve seen so far is not good,”. Most of the children have not recovered use of the most severely affected limb, although some recovery has been seen in less-affected limbs. The condition is associated with “severe weakness,”. “It’s not just dropping a toy; it’s more like not being able to move your arm at all.”

More common — and more concerning to health officials — is enterovirus 71, which was discovered by the same California lab in 1969. Enterovirus 71 is usually associated with severe neurological issues, including aseptic meningitis, polio-like paralysis and encephalitis. Waubant is not sure if the samples from this latest group of patients were tested for enterovirus 71.‘

Note: ‘All five children had been vaccinated against the poliovirus.‘

‘Global eradication of poliomyelitis may soon be achieved (by covering up the fact that Polio has been replaced by a more virulent strain known as Non-Polio Acute Flaccid Paralysis), but circulating polioviruses (via UN Mass Vaccination eugenics programs) could reemerge (by design) years after eradication (lies) by reversion of live attenuated oral vaccine virus to a virulent form (chemically synthesized, laboratory produced, weaponized version), laboratory stock mishandling (deliberate), or (UN/CDC sponsored) bioterrorism. If (when) a poliomyelitis outbreak occurs in the United States, access to a vaccine stockpile to interrupt (proliferate) viral spread will be necessary (to seed a whole new generation with Polio).’ Pamela C. Jenkins, MD, PhD, John F. Modlin, MD, American Academy of Pediatrics

Note: ‘If a poliomyelitis outbreak occurs in the United States, access to a vaccine stockpile to interrupt viral spread will be necessary.’

‘The last imported case caused by wild poliovirus into the United States was reported in 1993. The remaining 154 cases were vaccine-associated paralytic polio (VAPP) caused by live oral poliovirus vaccine (OPV).’

‘In 1999, to eliminate the risk for vaccine-associated paralytic poliomyelitis (VAPP), exclusive use of inactivated poliovirus vaccine (IPV) was recommended for routine vaccination in the United States. However, because of superior ability to induce intestinal immunity and to prevent spread among close contacts, OPV remains the vaccine of choice for areas where wild poliovirus is still present. Until worldwide eradication of poliovirus is accomplished, continued vaccination of the U.S. population against poliovirus will be necessary.’ Advisory Committee on Immunization Practices (ACIP)

‘Researchers have demonstrated that a polio virus can be reduced to a chemical, and assembled by following its written genetic code. (Viruses are not live organisms, they are sequences of genes that must rely upon entry into a host cell nucleus to utilize the cell’s genetic mechanisms for reproduction). When a synthetically-created polio virus was introduced into the spinal cords of mice it created the same paralysis seen in polio.‘ Bill Sardi

Chemical Synthesis of Poliovirus cDNA: Generation of Infectious Virus in the Absence of Natural Template – ‘Full-length poliovirus complementary DNA (cDNA) was synthesized by assembling oligonucleotides of plus and minus strand polarity. The synthetic poliovirus cDNA was transcribed by RNA polymerase into viral RNA, which translated and replicated in a cell-free extract, resulting in the de novo synthesis of infectious poliovirus. Experiments in tissue culture using neutralizing antibodies and CD155 receptor–specific antibodies and neurovirulence tests inCD155 transgenic mice confirmed that the synthetic virus had biochemical and pathogenic characteristics of poliovirus. Our results show that it is possible to synthesize an infectious agent by in vitro chemical-biochemical means solely by following instructions from a written sequence.’ Jeronimo Cello, Aniko V. Paul, Eckard Wimmer/August 2002

‘A vaccine-derived poliovirus is a strain of poliovirus, initially contained in the live oral polio vaccine, that has changed over time; it behaves more like a wild or naturally occurring virus. This means that it can be more easily spread to others who are unvaccinated against polio and who come in contact with the stool or oral secretions, such as saliva, of an infected person. These viruses may cause illness, including paralytic poliomyelitis.‘

‘Viral Nucleic Acids in Live-Attenuated Vaccines: Detection of Minority Variants and an Adventitious Virus – 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. 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.’ Journal of Virology, June 2010 vol. 84 no. 12

“The sequence of its genome is known and modern biotechnology allows it to be resurrected at any time in the lab. Man can thus never let down his guard against poliovirus.” Dr.s Vashisht & Puliyel of the Department of Paediatrics at St Stephens Hospital in Delhi, India

‘The anticipated detection of endogenous retroviral sequences (hybrid cancer causing ‘remnants of ancestral exogenous retroviral infections fixed in the germ-line DNA to which it has been exposed, including viral and bacterial vaccines‘) from the producer primate cells was confirmed… simian retrovirus (SRV) was present as genetically defective DNA.’

Note: ‘Mutations and minority variants, relative to vaccine strains, not known (deliberately ignored) to affect attenuation were detected in OPV (Trivalent Oral Poliovirus Vaccine).’

‘Trivalent oral polio vaccine faces ban – Experts say chances of vaccine derived polio virus infection (VDPV) are higher with the use of TOPV (that targets all three strains of polio virus – P1, P2 and P3) against the bivalent vaccine (that targets only P1 and P3).‘ Times of India, New Delhi, 01/20/2012

Monovalent Type 1 Poliomyelitis Vaccine, Live (Oral)/mOPV Type 1: DESCRIPTION (Substrate – Monkey Kidney Cells) The live monovalent Oral Polio Type 1 Vaccine (mOPV Type 1) contains suspension of live attenuated poliomyelitis type 1 virus (Sabin strain) prepared in Monkey Kidney cells. Each dose contains not less than 106.0CCID50 virus concentration of type 1. MgCI21M is used as a stabilizer and phenol red as an indicator. During formulation of mOPV Type 1 trace amounts of antibiotics: Kanamycin & Neomycin Sulphate are added. Manufactured by Panacea Biotec.

Note: ‘Monovalent oral polio vaccines are recommended for use in supplementary immunization campaigns in areas where only wild poliovirus type 1 or type 3 alone is circulating. It is not recommended as a substitute for OPV in routine immunization programmes. Two doses of mOPV administered within two weeks forms the basis of the new Short Interval Additional Dose (SIAD) approach, which is intended to rapidly boost population immunity in Asia.’ Global Polio Eradication Initiative

The endless domino-effect of cross-border NPAFP viral shedding has already begun manifesting: ‘…while India chalked up a year of being polio free, four other countries, Angola, Chad, the Democratic Republic of Congo and Sudan, have had year-long outbreaks. Another 13 countries have had recent infections – eight in Africa, along with Nepal, Kazakhstan, Tajikistan, Turkmenistan and Russia.’

The original Salk & Sabin Polio vaccine spawned a host of hitherto rare/unseen/unknown malignant forms of Cancer & crippling/debilitating neuro-developmental/neurological Syndromes & Disorders, which has provided a bonanza of surplus wealth to the Western Medical Establishment.

The short-list includes: Mesothelioma (fatal tumor of the membrane surrounding the lungs), Brain Cancers ( Ependymomas & Choroid Plexus Tumors, Astrocytomas, Glioblastomas, Medulloblastoma, Meningiomas), Bone Cancers (Osteosarcomas, Chondrosarcoma & Giant Cell Tumors), Post-Polio Syndrome, Myalgic Encephalomyelitis, Aseptic Meningitis, Non-Hodgkin Lymphoma & Chronic Fatigue Syndrome.

Note: These Cancer Epidemics were never seen before or very rarely before 50-60 years ago.

Thanks to Bill Gates and the World Health Organization’s relentless assault on Third World Nations, force-vaccinating countless local communities with an oral (live) Polio vaccine that has been officially banned in the United States and elsewhere, we can now add Non-Polio Acute Flaccid Paralysis to that list.

However the African Green Monkey Conundrum is unfortunately not isolated to the Polio Inoculations, in terms of identifying all Vaccine derived sources of cross-contamination seeping into the human population & gene pool.

Human Diploid Cells (aborted fetal tissue) provide the “Cell culture” in which vaccine formulas are often grown/nurtured; including the Inactivated Polio Vaccine/IPV, Oral live virus Polio Drops, Hepatitis A vaccine, Measles, Mumps, Rubella vaccine/MMR – Rubella component, Varicella (Chickenpox) vaccine, Rabies vaccine.

All Standard immunization vaccines in circulation requiring Human Diploid Cells (HDC), including those discontinued vaccines which utilized HDC since its inception in 1961, have derived the cell strain culture itself from one exclusive, carefully guarded “batch” or stockpile; comprising the fetal remains (lung tissue) of a female fetus of 3-months gestation (acquired in 1961/US), and those of a terminated 14-week-old male fetus (acquired in 1966/UK).

Human Fetal Links with Some Vaccines; ‘Human diploid cells are batches of human cells that are grown in a laboratory. Unlike cancer cells, they have the same number of chromosomes as normal human cells. Certain diploid cell strains are valuable in vaccine manufacture because these cells can be used for a very long period of time in the laboratory and are a reliable means by which many viruses that infect humans can be successfully and easily grown. Vaccines prepared in human diploid cells have proven to be very safe over the past several decades.

Two different strains of human diploid cell cultures made from fetuses have been used extensively for vaccine production for decades. One was developed in the United States in 1961 (called WI-38) and the other in the United Kingdom in 1966 (called MRC-5). WI-38 came from lung cells from a female fetus of 3-months gestation and MRC-5 was developed from lung cells from a 14-week-old male fetus. Both fetuses were intentionally aborted, but neither was aborted for the purpose of obtaining diploid cells.123. The fetal tissues that eventually became WI-38 and the MRC-5 cell cultures were removed from fetuses that were dead. The cellular biologists who made the cell cultures did not induce the abortions.

These two cell strains have been growing under laboratory conditions for more than 35 years. The cells are merely the biological system in which the viruses are grown. These cell strains do not and cannot form a complete organism and do not constitute a potential human being. The cells reproduce themselves, so there is no need to abort additional fetuses to sustain the culture supply. Viruses are collected from the diploid cell cultures and then processed further to produce the vaccine itself.’ National Network For Immunization Information

WI-38 came from lung cells from a female fetus of 3-months (terminated during the 1st Trimester) gestation: ‘Minced preparations were obtained by cutting the tissue in a Petri dish containing GM (growth medium) with paired scalpels or a scissors until the size of each piece approximated l-4 mm3. Fragmented preparations were obtained by tearing apart the tissue with two pairs of forceps in a Petri dish containing GM until the pieces could no longer conveniently be grasped and shredded. The entire contents of the dish were emptied into one or more Pyrex Blake bottles (surface area 100 cmZ), depending on the size of the original starting tissue. The fragmented lungs, for example, from a three-month-old human fetus were usually placed in four Blake bottles. Treatment of tissue with trypsin was done, in general, according to the method of Fernandes.’

‘The WI-38 and MRC-5 cell cultures have been used to prepare hundreds of millions of doses of (following) vaccines – rubella (third component of the MMR series, administered in 2 doses, first at 12 months old), hepatitis A (administered in 2 doses, first at 12 months old), varicella (chickenpox, administered in 2 doses, first at 12 months old) and rabies (administered selectively pending rabies-related emergency).‘ National Network for Immunization Information

When a human life is cut short in utero, then reduced to “minced (meat) preparations of tissue in a Petri dish”…”torn apart with two pairs of forceps until the pieces could no longer conveniently be grasped and shredded”, labelled as “cell strains (which) do not and cannot form a complete organism and do not constitute a potential human being”, all in the name of scientific progress, you know something is definitely wrong with the ethical parameters supporting Modern Medical research. Mother & baby-to-be share the same Immune System, during all three trimesters, while the Fetus is ‘in Utero’, via the Placenta.

Note: Given a mother (or father) already has a compromised Immune System and/or pre-existing Medical conditions, any such infection/disorder/disease will often factor into the equation; in terms of co-infecting/altering the DNA genetic blueprint of the offspring/progeny.

The introduction of Human Diploid Cells for use in Vaccine Technology followed closely on the heels of the disastrous Salk & Sabin Polio inoculation campaign; both in the United States (1954-55) and subsequently in Britain (1957). ‘The introduction of polio immunisation was accompanied by mass campaigns targeted at all individuals aged less than 40 years.‘

– a time-frame where-in either set of PARENTS from which the Human Diploid Cells specimens were acquired could obviously have been previously vaccinated with the Salk live Poliomavirus vaccine.

Therefore, the specimens which comprise the exclusive Human Diploid Cell culture stockpile may very well have “inadvertently” been co-infected with Simian Virus SV40 (diseased Rhesus & African Green Monkey tissue culture – strain utilized to nurture Poliomyelitis, hidden in the germ line DNA of either Fetus – the result of direct SV40 contamination from the Salk Vaccine (live Poliomavirus) co-infecting the DNA of either set of parents responsible for the baby’s genetic material now in widespread use; subsequently passed on from mother to Fetus via the Placenta.

An entire generation has since been inoculated with vaccines containing the original Human Diploid Cell culture set. If, indeed, there was any SV40 cross-contamination embedded in the lung tissue culture extracted from either Fetus, the primary HDC source in circulation, it is logical to determine that SV40 cross-contamination has also made its way into those who were subsequently vaccinated (intramuscularly, subcutaneously or via oral drops) with the same Human Diploid Cell culture source.

This would certainly explain the recent Controlled Study where-in Simian Virus co-infection was identified in 67% of post-mortem brains of sufferers of Autism.

New Controlled Study finds poliomavirus infection in post-mortem brains of sufferers of Autism – 67% infection with Simian Virus (SV40): ‘Vertical viral transmission represents a nongenetic mechanism of disease compatible with high parent-to-offspring transmission and with low rates of disease-specific genetic abnormalities. Vertically transmitted viruses should be found more frequently in the affected tissues of autistic individuals compared to controls. Our initial step was thus to assess by nested polymerase chain reaction (PCR) and DNA sequence analysis the presence of cytomegalovirus (CMV), Epstein-Barr virus (EBV), herpes simplex virus type 1 (HSV1), herpes simplex virus type 2 (HSV2), human herpes virus 6 (HHV6), BK virus (BKV), JC virus (JCV), and simian virus 40 (SV40) in genomic DNA extracted from postmortem temporocortical tissue (Brodmann areas 41/42) belonging to 15 autistic patients and 13 controls. BKV, JCV, and SV40 combined are significantly more frequent among autistic patients compared to controls (67% versus 23%, respectively; P <.05). The majority of positives yielded archetypal sequences, whereas six patients and two controls unveiled single–base pair changes in two or more sequenced clones.’ Laboratory of Molecular Psychiatry, Psychiatric Genetics/Neurogenetics, University Campus Bio-Medico, Rome, Italy

How did Simian Virus get there, you might ask? – inevitably the result of vertical transmission, viral shedding & inter-generational cross-contamination from Salk & Sabin Polio inoculations, sugar cube/oral drops versions & the subsequent Inactivated Polio Vaccine (or IPV) now on the schedule; fixed in the germ-line DNA of newborns.

‘In recent years more than 60 scientific studies have found SV40 in rare human brain, bone and lung-related cancers, the same kinds of tumors the virus caused in laboratory animals. Some scientists believe SV40 may play a role in causing those cancers. One of the biggest mysteries, however, is why SV40 has been found in tumors removed from people who never received the contaminated Salk vaccine.‘

There are several possible explanations for this disturbing anomaly:

1. Direct SV40 cross-contamination from the Salk Vaccine (live Poliomavirus) co-infecting the DNA of either set of parents responsible for the baby’s genetic material now in use; passed on from mother to child via the Placenta & Colostrum (Endogenous retrovirus).

2. Direct SV40 cross-contamination of the child’s DNA (germ-line mutations) from the Salk Vaccine (live Poliomavirus), embedded in the Brain white-matter.

3. Indirect SV40 contamination from another vaccine (ie. Inactivated Polio – African Green Monkey Monkey Kidney “benign” version, Oral Polio drops – African Green Monkey Monkey Kidney “benign” version), co-infecting the DNA of either set of parents responsible for the baby’s genetic material now in use; passed on from mother to child via the Placenta & Colostrum (Endogenous retrovirus).

4. Indirect SV40 contamination from a vaccine derived from contaminated Human Diploid Cell culture (ie. Inactivated Polio, Oral Polio Drops, Hepatitis A, Measles, MMR – Rubella component) co-infecting the DNA of either set of parents responsible for the baby’s genetic material now in use; passed on from mother to child via the Placenta & Colostrum (Endogenous retrovirus).

5. Indirect SV40 contamination from a vaccine derived from contaminated Human Diploid Cell culture (ie. Inactivated Polio, Oral Polio Drops, Hepatitis A, Measles, MMR – Rubella component) co-infecting the child.

6. Indirect SV40 contamination from another Polio type vaccine (ie. Inactivated Polio – African Green Monkey Monkey Kidney “benign” version, Oral Polio drops – African Green Monkey Monkey Kidney “benign” version) co-infecting the child.

‘SV40 is a poliomavirus with double-stranded circular DNA…Important roles of the early proteins in TSG, oncogene and growth factor regulation…SV40Tag can bind to and inhibit p53 and pRb TSGs, and SV40tag has been shown to inhibit PP2A, which may lead to the activation of Wnt and ERK signaling pathways. SV40 infection may also increase autocrine and paracrine signaling through a variety of growth factor pathways and induce the expression of telomerase. SV40 infection may increase the transcription and activation of Notch–1, which may have an important role in mesothelial cell transformation and proliferation…in vivo evidence from mesothelioma samples. 10 out of 11 tumors with detectable SV40Tag expression also stained positively for activated Akt (protein kinase that plays a key role in multiple cellular processes such as glucose metabolism, cell proliferation, apoptosis, transcription and cell migration).

From 1955 to 1963, the polio vaccine supplied to the United States, Canada, Europe, Asia and Africa was contaminated with SV40. Furthermore, the possibility of horizontal transmission may have enlarged this exposure. Many studies have found evidence of SV40 infection. A meta-analysis conducted by Vilchez reviewed molecular, pathological, and clinical data from 1,793 cancer patients. He concluded that there is significant data to support a role for SV40 infection in human brain cancers, bone cancers, malignant mesothelioma, and non-Hodgkin’s lymphoma.’ Cleveland College of Medicine

The multi-billion dollar Vaccine Industry has routinely been utilizing Human Diploid Cells gathered from sections of a mere two individual Fetuses. But these select babies-to-be didn’t come out of thin air…they’re not Adam & Eve either. Their individual DNA genetic blueprints, the unique germ line DNA of either Fetus was determined by each set of parents, whose own individual DNA genetic blueprint, each unique set of germ-line DNA was previously determined by their own set of parents, etc etc etc. This has everything to do with history. Endogenous retroviruses – remnants of ancestral exogenous retroviral infections fixed in the germline DNA. And remember, they were both conceived during one of the darkest chapters in Modern Medical history – that of the disastrous, misguided Salk & Sabin Polio Vaccine campaign.

Based on the current evidence, including that established in VRM: PCV Vaccine Exposed – Breeding Ground For Staphylococcus Aureus, where-in, ‘All vaccinated children in the Western hemisphere are now carriers of what is known as MRSA (Methicillin-resistant Staphylococcus  aureus/antibiotic resistant “Superbug”), due to cross-infection primarily from the routine administering of the Pneumococcal (PCV) Vaccine – in combination with post vaccination antibiotic & antiviral drug treatment, an accumulative assault which strips a child of his/her natural anti-biotic resistance whilst infecting them with a host of bacterial serotypes (1, 3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F, 23F)’, it now becomes clear that each successive generation of vaccinated children have become the unwitting hosts to a deadly form of genetic roulette, an ideal breeding ground for the proliferation and weaponizing of viral & bacterial infections; their capacity for natural immunity threatened immeasurably by a “synergistic” convergence of these harmful, chemically synthesized toxins.

The hubris of the Medical Industry, an ever growing, centralized Technocracy of compartmentalized, overpaid bureaucrats & blindsighted “elites” capable of justifying injecting “genetically defective DNA” into the bloodstream of babies & young children, puposefully exposing them to cancer-causing “endogenous retroviral sequences from primate cells“, defies all reason, and runs counter to every so-called standard of “Do no harm” type medicine once held sacred by those doctors working on the front lines, in whom our communities have placed their sacred trust for generations.

There is simply no middle ground, no compromise position in determining the merits of Vaccine safety & efficacy, the whole basis for & methodology behind Immunization as a means of overcoming viral & bacterial type infections and theoretically safeguarding the body’s immunological capacity. Either you are FOR Immunization or firmly AGAINST it. Those parents who subscribe to the belief that they are somehow erring on the side of cautionary wisdom by allowing their child/children to be vaccinated gradually or partially, according to the current Standard Immunization Schedule established by the CDC & local Government appointed Health “experts”, are woefully mistaken. The ENTIRE Vaccine Industry is a fraud, period. All vaccines, by their very nature, play off each other – a “synergistic” chain-reaction; triggering further infections & disorders. In many cases the very signature disease/disorder they claim to protect you against is PRECISELY that which they inadvertently spread.

Concentrated doses of Ascorbic Acid (Vitamin C) cleanse all viral pathogens from the body, including strains of Polio, Measles, Chickenpox & Hepatitis.

‘In poliomyelitis, vitamin C (6,000 to 20,000 mg are administered in a twenty-four hour period intravenously, intramuscularly, and/or orally – “at least 350 mg per kilogram of body weight.”) performs three important functions:

1) It destroys the virus;
2) acting as the dehydrator and diuretic of first choice, it removes the edema fluid from the brain and the cord;
3) it preserves the lining of the central canal and maintains more regular spacing and less crowding of the ependymal cells (Altman). The pressure within the bony vault of the central nervous system resulting from the inflammatory process excited by the virus, acts as a haemostat to cut off the blood supply to the anterior horn cells. This compression of their vessels denies to the horn cells the essentials for function, for life even.‘

Excerpt from ‘Massive Doses of Vitamin C and the Virus Diseases‘ report by F. R. KLENNER, M.D., Reidsville, North Carolina/April 1951

Note: “With 350 mg per kilogram of body weight every two hours, he could stop measles and dry up chicken pox.” Lendon H. Smith/Clinical Guide to the Use of Vitamin C: The Clinical Experiences of Frederick R. Klenner, M.D

‘Klenner used vitamin C, often accompanied with high doses of other nutrients, to fight a striking variety of other illnesses (including) Rocky Mountain Spotted Fever, bladder infections, alcoholism, arthritis, leukemia, atherosclerosis, ruptured intervertebral discs, high cholesterol, corneal ulcer, diabetes, glaucoma, burns and secondary infections, heat stroke, radiation burns, heavy metal poisoning, chronic fatigue, and complications resulting from surgery. Additionally, Klenner also reported mega nutrient cures of tetanus, trichinosis, venomous bites from spiders or snakes, and, perhaps most controversially, multiple sclerosis.‘ Andrew W. Saul, Journal of Orthomolecular Medicine

“Some physicians would stand by and see their patient die rather than use ascorbic acid because in their finite minds it exists only as a vitamin.” Frederick. R. Klenner, MD

“When I first came across Klenner’s work on polio patients, I was absolutely amazed and even a bit overwhelmed at what I read. . .To know that polio had been easily cured and so many babies, children, and some adults still continued to die or survive to be permanently crippled by this virus was extremely difficult to accept.

Many viral infectious diseases have been cured and can continue to be cured by the proper administration of Vitamin C. Yes, the vaccinations for these treatable infectious diseases are completely unnecessary when one has the access to proper treatment with vitamin C. And, yes, all the side effects of vaccinations are also completely unnecessary since the vaccinations do not have to be given in the first place with the availability of properly dosed vitamin C.

Amazingly, vitamin C has actually already been documented in the medical literature to have readily and consistently cured both acute polio and acute hepatitis, two viral diseases still considered by modern medicine to be incurable.” Dr. Thomas E. Levy, MD, JD

My point is, Health Authorities are doing a great disservice to families, by not providing this information in a fair and open discussion.

Natural Immunity is designed to take on and withstand any incoming infections which threaten your survival. The body can only do this when it is naturally, gradually exposed to disease & infectious agents lurking in the environment. 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 injecting toxins into deep muscle tissue/subcutaneously, artificially shocking or jump-starting the body into recognizing external “threats”, rather than holistically EMBRACING all that we come in contact with, thereby re-enforcing, through HARMONY, the inherent properties of natural immunity. We’re not meant to be hermetically sealed organisms, but that is ultimately where the Medical Establishment intends you to be. And if you take their instructions to heart, then your body will inevitably become a breeding ground for long-term infections, degeneration & disease, neurological disruption …and ultimately, a perfect environment for otherwise AVOIDABLE hybrid forms of cancer.

Our ancestors were altogether tougher than we are today, having had no choice but to embrace the wisdom of natural health in order to survive. They were deeply connected with their environment and wisely passed on their knowledge of dietary & herbal remedies (balms, tinctures, broths, etc) from generation to generation; the single greatest threat – a lack of proper sanitation, hygiene & nutrition. In point of fact, despite claims of “progress” during the birth of the Industrial Age, settlers & homesteaders were routinely driven off the land which sustained them and herded into conditions of urban squalor. Gradually, somewhere along the road, we abdicated our role as leaders within the community, delegated private or elected committees & councils to determine the course of health freedom.

I challenge you to break the shackles of addiction which have prevented many of us from fully embracing our inherent natural immunity, to return to that path on which our ancestors still stand, and rediscover an independent strength of will forever coursing through your veins. Once you set foot on that road, you may never lay claim to false promises or misguided Institutions of so-called Medicine ever again. Godspeed & good riddance, as they say. May natural immunity be your guiding light through these uncertain times ahead. Words to live by. Amen. VRM

See: VRM: Polio – United Nations & The Great Cull

See: VRM: The Re-emergence of Polio in The Third World (compliments of the World Health Organization & Bill Gates)

Related articles:

VRM: The Autism Report http://vaccineresistancemovement.org/?p=10185

VRM Worldwide Autism Study Direct link to study: http://study.vaccineresistancemovement.org/

VRM: The Problem With Vaccines Part 1 http://vaccineresistancemovement.org/?p=488

VRM: Vaccine Clinic – A Concise Compendium To The Problem With Vaccines http://vaccineresistancemovement.org/?p=6278

VRM: The Problem With Vaccines Part 2 – Synergistic Effect of Heavy Metal Toxicity On The Body http://vaccineresistancemovement.org/?p=6097

VRM: The Problem With Vaccines Part 3 – Synthetic Genomics & The Death Of Natural Immunity http://vaccineresistancemovement.org/?p=6880

VRM: A Concise Compendium To The Problem With Vaccines Part 3 – Synthetic Genomics & The Death Of Natural Immunity http://vaccineresistancemovement.org/?p=7283

VRM: The Problem With Vaccines Part 4 – Primary Aspects of Vaccine Toxicity Affecting Body http://vaccineresistancemovement.org/?p=8787

VRM: The Problem With Vaccines Part 5A – Detoxification & Restoration of the Body http://vaccineresistancemovement.org/?p=8836

VRM: The Problem With Vaccines Part 5B – Detoxification & Restoration of the Body http://vaccineresistancemovement.org/?p=8847

VRM: PCV Vaccine Exposed – Breeding Ground For Staphylococcus Aureus http://vaccineresistancemovement.org/?p=9431

VRM: The Rise of Mutagenic Viruses http://vaccineresistancemovement.org/?p=13124

VRM: Pandemic Preparedness & The Dark Agenda Ahead http://vaccineresistancemovement.org/?p=9460

VRM: Mandatory Vaccinations – How They Will Be Implemented http://vaccineresistancemovement.org/?p=11806

VRM: The Flu Report http://vaccineresistancemovement.org/?p=9226

VRM: 5 Reasons Not To Get The Flu Shot http://vaccineresistancemovement.org/?p=12642

VRM: Vaccine Ingredients http://vaccineresistancemovement.org/?p=979

VRM: Safe Alternatives to Vaccines http://vaccineresistancemovement.org/?p=662%EF%BB%BF

VRM: Family Charts Gradual Decline Of Daughter http://vaccineresistancemovement.org/?p=3156

VRM: Health Matters Part 1 http://vaccineresistancemovement.org/?p=6719

VRM: Health Matters Part 2 http://vaccineresistancemovement.org/?p=6746%EF%BB%BF

VRM: Alternative Cancer Cures That Work http://vaccineresistancemovement.org/?p=3729

VRM: Pregnancy Tips http://vaccineresistancemovement.org/?p=3270

VRM: H1N1 Shot Reactions – Miscarriages http://vaccineresistancemovement.org/?p=943

VRM: The Vanishing Sperm Count http://vaccineresistancemovement.org/?p=4639

VRM: H1N1 Vaccine Surplus From 2009 Reveals Growing Distrust of Gov’t & WHO http://vaccineresistancemovement.org/?p=4969

VRM: Flu Death Statistics – WHO & The Big Lie http://vaccineresistancemovement.org/?p=784

VRM: Vaccine Industry Deception, Propaganda & Media Collusion http://vaccineresistancemovement.org/?p=197

VRM: Birth of Medical & Scientific Dictatorship – Future Scenarios http://vaccineresistancemovement.org/?p=997

VRM: H1N1 Bio-weaponry Incorporated http://vaccineresistancemovement.org/?p=884

VRM: Aids & The WHO Connection – Criminal Intent http://vaccineresistancemovement.org/?p=1749

VRM: Morgellons Syndrome & Chemtrails http://vaccineresistancemovement.org/?p=839

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

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

VRM: The Rockefeller Foundation Drafts A Post-Pandemic Scenario http://vaccineresistancemovement.org/?p=5102

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

VRM Live – 01/28/11: Vaccine Resistance Movement founder Joel Lord discusses Synthetic Genomics, cloned cell vaccine technology & the death of natural immunity, gutter journalism & Dr. Wakefield’s imminent vindication with ‘Truth to Power’ host Paul Mabelis. http://www.blogtalkradio.com/empradio/2011/01/28/truth-to-power-thursday

VRM Live – 11/04/10: Vaccine Resistance Movement founder Joel Lord lays out the whole vaccine process with Paul Mabelis; including heavy metal toxicity, synergy, 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

VRM Live – 09/24/10: Vaccine Resistance Movement Founder Joel Lord & activist/radio host Jesse Calhoun lay it all out tonite. Topics include the VRM Worldwide Autism Study, Scientific/Medical 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

If you appreciate the efforts to bring this information forward do consider making a donation. Any amount, no matter how small will help enable me to carry on this invaluable research. See Paypal link on the VRM website (click on ‘Donate’ tab in upper right corner). Thank you all.
18 Responses to “VRM: Weaponized Polio & The African Green Monkey Conundrum”
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- HomoeopathyInfo » The entire vaccine program is based on a massive Fraud. on April 18, 2013
  
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VRM: Weaponized Polio & The African Green Monkey Conundrum

18 Responses to “VRM: Weaponized Polio & The African Green Monkey Conundrum”

VRM: Alternative Cancer Cures That Work & Your Government Still Can’t Ban them From Use! « Vaccine Resistance Movement on March 3, 2017

VRM: SB277 Road To Tyranny « Vaccine Resistance Movement on August 15, 2016

VRM: Mycoplasma – Rogue Pathogen in Vaccines « Vaccine Resistance Movement on April 26, 2016

VRM: Gardasil/Cervarix – A Legacy Of Shame « Vaccine Resistance Movement on February 10, 2016

VRM: Genetic Engineering & The Next Pandemic « Vaccine Resistance Movement on February 2, 2016

VRM: Measles Report « Vaccine Resistance Movement on November 4, 2015

VRM: The Autism Report Part 2 – Missing Link « Vaccine Resistance Movement on October 4, 2015

VRM: The Rise of Mutagenic Viruses « Vaccine Resistance Movement on September 14, 2015

VRM: Vaccine Ingredients « Vaccine Resistance Movement on October 23, 2013

VRM: Gardasil/Cervarix Part 2 – Demyelination, Multiple Sclerosis & the Copaxone Connection « Vaccine Resistance Movement on October 9, 2013

VRM: Aids & The WHO Connection – Criminal Intent « Vaccine Resistance Movement on October 8, 2013

VRM: First Strike – The Dark Side of The Vitamin K Shot « Vaccine Resistance Movement on October 5, 2013

VRM: The Re-emergence of Polio in The Third World (compliments of the World Health Organization & Bill Gates) « Vaccine Resistance Movement on September 29, 2013

HomoeopathyInfo » The entire vaccine program is based on a massive Fraud. on April 18, 2013

VRM: Vaccine Exemptions – Protecting Human Rights & Voluntary Consent « Vaccine Resistance Movement on November 1, 2012

Cancer – more info on alternative remedies « BIO-SIL SOUTH AFRICA Blog on October 6, 2012

VRM: Weaponized Polio & The African Green Monkey Conundrum | Health News Site on September 21, 2012

VRM: Weaponized Polio & The African Green Monkey Conundrum on September 21, 2012

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