‘Poliomyelitis (polio) is a highly infectious disease caused by a virus. It invades the nervous system, and can cause total paralysis in a matter of hours. It can strike at any age, but affects mainly children under three (over 50 percent of all cases). The virus enters the body through the mouth and multiplies in the intestine. Initial symptoms are fever, fatigue, headache, vomiting, stiffness in the neck and pain in the limbs. One in 200 infections leads to irreversible paralysis (usually in the legs). Among those paralyzed, 5 to 10 percent die when their breathing muscles become immobilized.
Although polio paralysis is the most visible sign of polio infection, fewer than 1 percent of polio infections ever result in paralysis. Poliovirus can spread widely before cases of paralysis are seen. As most people infected with poliovirus have no signs of illness, they are never aware they have been infected. After initial infection with poliovirus, the virus is shed intermittently in the feces (excrement) for several weeks. During that time, polio can spread rapidly through the community.
In the remaining polio endemic countries, poliovirus is spread from person to person through fecal-oral contact. Where hygiene and sanitation are poor, young children are especially at risk. Young children who are not yet toilet-trained are a ready source of transmission, regardless of their environment. Polio can be spread when food or drink is contaminated by feces. There is also evidence that flies can passively transfer poliovirus from feces to food.
Once established in the intestines, poliovirus can enter the blood stream and invade the central nervous system, spreading along nerve fibers. As it multiplies, the virus destroys nerve cells (motor neurons), which activate muscles. These nerve cells cannot be regenerated and the affected muscles no longer function. The muscles of the legs are affected more often than the arm muscles. The limb becomes floppy and lifeless a condition known as acute flaccid paralysis (AFP). More extensive paralysis, involving the trunk and muscles of the thorax and abdomen, can result in quadriplegia. In the most severe cases (bulbar polio), poliovirus attacks the motor neurons of the brain stem, reducing breathing capacity and causing difficulty in swallowing and speaking. Without respiratory support, bulbar polio can result in death.
non-polio acute flaccid paralysis
During 2011, incidence of Non-Polio Acute Flaccid Paralysis (clinically indistinguishable from polio paralysis but twice as deadlyincidence of NPAFP was directly proportional to doses of oral polio received) in India, alone, sky-rocketed 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” campaignWhile 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 (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. The same cross-contamination, hybrid Polio strain will concurrently be passed on, generation to generation, throughout impoverished areas, embedded in the baby’s genetic DNA material, via the mother’s placenta & colostrum.
Why is this issue so important? Because 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. They have now adopted a “case closed” approach to Polio in India & elsewhere, despite the exponential surge in numbers occurring throughout the Third World.
But instead of providing high quality, safe & efficacious Malaria treatment, community access to clean water, holistic dietary improvements ie. growing local natural food sources, and the independent means to sustain that infrastructure, The World Health Organization, CDC, NIH, all Government run Health Departments & those wealthy Philanthropists who have jumped on the bus & wrapped themselves around the same flag, are all fervently pushing the Polio Mass Vaccination Program on the Third World as some great savior and answer to our prayers.
‘About 1.2 billion people still have no access to safe drinking water, and 2.4 billion do not have adequate sanitation services. Some 2 million children die every year from water-related diseases.Money spent on vaccines when clean water and other diseases mostly ignored (45% of UNESCO funds is spent on vaccines)…
The experience in the early 1960s with SV40 contamination of poliovirus and adenovirus vaccines and the continuing questions regarding whether SV40 could be responsible for some human neoplasms underscore the importance of keeping viral vaccines free of adventitious agents. This is particularly important when there is a theoretical potential for contamination of a vaccine with viruses that might be associated with neoplasia. Because some mammalian tumors and some cells transformed by viruses contain infectious virus, cells transformed by an unknown mechanism have a theoretical risk of containing a transforming virus.’ FDA Report
Many here voice a silent view that the Salk and Sabin vaccine, being made of monkey tissue…has been directly responsible for the major increase in leukemia in this country.” Frederick Klenner M.D.

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 Salk Polio vaccine formula; contaminated with diseased African Green Monkey Kidney virus (Simian Virus/SV40), the follow-up Sabin formula (including the sugar cube version); and subsequently on 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 – which is now being forced on hundreds of thousands of children, otherwise symptom-free from Polio.
So what is the REAL smoking gun behind the so-called decline in numbers of Polio Paralysis/Infantile Paralysis in the Third World, officially attributed to the Globalist financed Polio Mass Vaccination (aka Eugenics) Programs?
Polio HAS come back with a vengeance, due to the WHO’s relentless quest to seed every child in the Third World (the majority of whom were otherwise symptom-free from Polio) with live attenuated poliomyelitis type 1 virus laced with Monkey Kidney cells (OPV drops); and the ensuing cross-infection & viral shedding which follows.
Since the Global Polio Eradication Initiative (GPEI) was launched in 1988 (spearheaded by national governments, the World Health Organization/WHO, Rotary International, the US Centers for Disease Control and Prevention/CDC & UNICEF, supported by key partners including the Bill & Melinda Gates Foundation), India has seen an exponential surge, year to year, in cases of Acute Flaccid Paralysis (AFP), in direct proportion to the increasing intensity of Polio immuniozation being conducted on the ground throughout India’s many provinces.
‘The number of polio cases worldwide dropped to its lowest recorded point last year, but the campaign to eradicate the virus could be undermined by regional conflict and a funding shortfall, the World Health Organization has warned. Only 537 cases of polio, an infectious disease that mainly affects children under 5, were reported in 2001, down 82 percent from a year earlier, when the number was 2,979, the United Nations agency said. It also reported that the number of countries reporting continued polio transmission was cut in half, to 10. The health organization began its campaign against polio in 1988, when it still cut a swath through more than 125 countries, paralyzing children at the rate of 1,000 every day. The group says it aims to eliminate polio by the end of this year and certify the world polio-free at the close of 2005.
The data on acute flaccid paralysis (AFP) cases from Uttar Pradesh (UP) presented are for the year 2005. Through the Right to Information (RTI) Act, we have been able to obtain data collected by the National Polio Surveillance Project (NPSP) for 2006. At 47 wk ending in 2006, of a total of 10,879 cases of AFP, only 2,043 were followed up. Of these, 989 (48.4%) had residual paralysis, which would qualify them to be diagnosed clinically as polio cases, and 244 (11.9%) deaths. If these rates are extrapolated to the total number of reported AFP cases, the total cases with residual paralysis work out to be 5,265 and the number of deaths to be 1,294. These numbers are higher than that presented by Puliyel et al indicating an escalation of the problem from 2005 to 2006. From the rates of death and residual paralysis in the nonpolio AFP cases calculated from data at 47 wk, 2006, it appears that children who were identified as AFP cases and classified as non-polio AFP by NPSP, are more than twice at risk of dying than the wild polio virus (WPV) (or vaccine virus cases) and the difference is statistically significant (P<0.001).‘ C. Sathyamala, Council for Social Development, New Delhi, India, 05/2007
‘Experts call WHO & Bill Gates Foundation’s role in India’s polio eradication campaign unethical: Medical experts in paediatrics in the country have lambasted the World Health Organisation (WHO) and the Bill Gates Foundation for trumpeting India’s polio eradication campaign which they knew 10 years back that it was never going to succeed. ‘India was taken off the list of polio-endemic countries by the WHO on January 12, 2012 but the polio eradication campaign will have to be continued in some format for ever. The long promised monetary benefits from ceasing to vaccinate against poliovirus will never be achieved’, the well known paediatricians said.
“It was unethical for WHO and Bill Gates to flog this programme when they knew 10 years back that it was never to succeed. Getting poor countries to expend their scarce resources on an impossible dream over the last 10 years was unethical,” said Dr Neetu Vashisht and Dr Jacob Puliyel of the Department of Paediatrics at St Stephens Hospital in Delhi in their report in the April issue of ‘Indian Journal of Medical Ethics’. In the remaining polio endemic countries, poliovirus is spread from person to person through fecal-oral contact. Where hygiene and sanitation are poor, young children are especially at risk. Young children who are not yet toilet-trained are a ready source of transmission, regardless of their environment. Polio can be spread when food or drink is contaminated by feces. There is also evidence that flies can passively transfer poliovirus from feces to food.’ Ramesh Shankar, Mumbai, India
Experts fear the disease could “come back with a vengeance”. The World Health Organization says polio is “at a tipping point”. There have been large outbreaks of the virus in Africa, Tajikistan and China has had its first cases for more than a decade. “Over the last 24 months on three continents – in Europe, in Africa and in Asia – we have seen horrific explosive outbreaks of the disease that affected adults, and in some cases 50% of them died. What it reminded people is that, if eradication fails, we are going to see an huge and vicious upsurge of this disease with consequences that it is very difficult even to foresee right now.” Bruce Aylward, head of the WHO’s polio eradication campaign. He said the initiative was “now on an emergency footing” which would result in a “big shift” in the way the virus is tackled. The strategy has been summarised as the “relentless pursuit of the unvaccinated child”.’
Monovalent Type 1 Poliomyelitis Vaccine, Live (Oral)/mOPV Type 1DESCRIPTION (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.
Monovalent Oral Polio Type 1 Vaccine (mOPV Type 1)/mOPV Type 1: DESCRIPTION (Substrate – Vero 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 Vero 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.
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.
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
The original Salk & Sabin Polio vaccine spawned a host of hitherto rare/unseen/unknown malignant forms of Cancer & crippling/debilitating neuro-devlopmental/neurological Syndromes & Disorders (which has provided a bonanza of surplus wealth to the Western Medical Establishment) including: 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.
We can now add Non-Polio Acute Flaccid Paralysis to that list. Thanks, in full, to the World Health Organization & Bill Gates.
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VRM Worldwide Autism Study
Direct link to study: http://study.vaccineresistancemovement.org/
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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 - 11/04/10Vaccine 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.
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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
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