‘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.
The poliovirus can also infect persons who have been vaccinated and can be carried by them. Such individuals will not develop polio (absolute lie), but can carry the virus in their intestines and can pass it to others in conditions of sub-standard hygiene. The disease may infect thousands of people, depending on the level of sanitation, before the first case of polio paralysis emerges. Individuals can carry the virus in their intestines just long enough to transmit to others.‘ Excerpt from World (Un)Health Organization (WHO) Polio “Eradication” Program” – Last Child Teaching Guide”
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, sky-rocketed to 60,478 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 (Simian Virus 40/SV40) inter-generational cross-contamination from the original Sabin Polio Vaccine (1961) compounded by the ongoing laboratory synthesis of the primary Salk Vaccine version (SV40 contaminated) Rhesus seed strain; 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 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.
‘Data from India on polio control over 10 years, available from the National Polio Surveillance Project, has now been compiled and made available online for it to be scrutinised by epidemiologists and statisticians. This shows that the non-polio AFP rate increases in proportion to the number of polio vaccine doses received in each area. Nationally, the non-polio AFP rate is now 12 times higher than expected. In the states of Uttar Pradesh (UP) and Bihar, which have pulse polio rounds nearly every month, the non-polio AFP rate is 25- and 35-fold higher than the international norms.
The relationship of the non-polio AFP rate is curvilinear with a more steep increase beyond six doses of OPV in one year. The non-polio AFP rate during the year best correlates to the cumulative doses received in the previous three years. Association (R2) of the non-polio AFP rate with OPV doses received in 2009 was 41.9%. Adding up doses received from 2007 increased the association (R2 = 55.6% p < 0.001). Population density did not show any association with the non-polio AFP rate, although others have suggested that it is related to polio AFP.‘ Dr. Neetu Vashisht and Dr. Jacob Puliyel, Department of Paediatrics, St Stephens Hospital, Delhi
‘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 faeces (excrement) for several weeks. During that time, polio can spread rapidly through the community.’ WHO Polio “Eradication” Program” – Last Child Teaching Guide”
‘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.‘ Arthur Schoenstadt, MD
‘It is worth noting that mutations are somewhat common with the oral polio vaccine (OPV), a live vaccine that is ingested instead of injected. The vaccine virus can mutate into a virulent form and result in rare cases of paralytic polio. For this reason, OPV is no longer used in the United States, and has been replaced on the Recommended Childhood Immunization Schedule by the inactivated polio vaccine (IPV).‘ College of Physicians, Philadelphia
‘At this juncture, the continued use of trivalent Oral Polio Vaccine (tOPV) in the polio eradication program poses the risk of paralysis from type 2 circulating Vaccine Derived Polio Virus (cVDPV). The Sabin type 2 in the tOPV has been responsible for > 90% of alcVDPV cases and about 40%cases of VAPP globally during the last few years. All countries will continue to face the risk of type 2 cVDPV as long as tOPV is being used in the program.‘ National Polio Surveillance Project/WHO, July 2013
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.
The WHO have made a terrible mistake & miscalculation here, conducting a “shell-game” of lies & misinformation, and they’ll clearly stop at nothing to erase their bloodied tracks. Too much money has been invested, too many international reputations are at stake, the nexus of a massive Private-Public enterprise implicating the majority of nations from around the world, hundreds of powerful Corporations, a host of prominent Philanthropists, including the influential Vaccine lobby & major Vaccine Manufacturers (reaping enormous profits via this venture); promoted fervently by the Corporate sell-out Mainstream Media machine. All sides are complicit in this crime against humanity.
This is also the heart of the 21st Century Eugenics Movement in action. The lives of millions of poor, voiceless children are being sacrificed, crushed & silenced under the wheels of forced evolutionary change, to accommodate a Globalist Medical Dictatorship hellbent on re-engineering & culling the human species. Natural health be damned; as real statistics are routinely being covered up and/or disguised by those Institutions the public has come to rely on (WHO, CDC, NIH), drowned out by Mainstream Media promulgated lies & propaganda driving this Technocratic Elitist agenda forward.
The Global Initiative to inoculate every child with the Oral live Polio drops, currently being subjected upon the poorest regions throughout the Third World, has been a complete abject disaster (as with all Mass Vaccination Initiatives ever conducted); having literally reawakened this sleeping giant, in the form of a new laboratory synthesized hybrid of Polio virus, currently manifesting as Non-Polio Acute Flaccid Paralysis. Expect more viral mutations to follow.
The truth is, Malaria, NOT Polio, has always represented the single greatest threat to survival in the poorest regions throughout the Third World – and the locals everywhere know it. ‘A third of malaria drugs used around the world to keep the spread of the disease at bay are counterfeit‘…“In Africa polio does not kill anybody and they say it’s very rare to catch. It’s really very rare to get paralytic polio. They say it’s in very rare circumstances, so what is it that is killing people in Africa? Malaria. Every five seconds a child is dying of malaria in Africa. Now to get the dose of life-saving anti-malaria is about $5 but there is no government to give anti-malaria.‘
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.
‘The charade about polio eradication and the great savings it will bring has persisted to date. It is a paradox, that while the director general of WHO, Margret Chan, and Bill Gates are trying to muster support for polio eradication it has been known to the scientific community, for over 10 years, that eradication of polio is impossible. This is because in 2002 scientists had synthesised a chemical called poliovirus in a test-tube with the empirical formula.
It has been demonstrated that by positioning the atoms in sequence, a particle can emerge with all the properties required for its proliferation and survival in nature. Wimmer writes that the test-tube synthesis of poliovirus has wiped out any possibility of eradicating poliovirus in the future. Poliovirus cannot be declared extinct because the sequence of its genome is known and modern biotechnology allows it to be resurrected at any time in vitro.’ Dr. Neetu Vashisht and Dr. Jacob Puliyel, Department of Paediatrics, St Stephens Hospital, Delhi
‘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 forcing of them to take a vaccine (Polio) against a disease they know to be harmless and which they know how to cure in its harmful state was seen as government hell bent on killing its own population for the benefit of commanding white world…The army and the police move house to house looking for children to vaccinate. At the same time, things that kill children like malaria, cholera, issues of stunted growth, sanitation, are completely untackled.“‘ Kihura Nkuba, Uganda
The live Oral drops version of the Polio Vaccine (OPV) has been banned in the United States. However, it is still being force-administered to impoverished communities under the thumb of the United Nations.
‘One concern that must be considered is the potential for the vaccine virus to revert to a form capable of causing disease. Mutations that can occur when the vaccine virus replicates in the body may result in more a virulent strain. This is very unlikely, as the vaccine virus’s ability to replicate at all is limited; however, it is taken into consideration when developing an attenuated vaccine.
It is worth noting that mutations are somewhat common with the oral polio vaccine (OPV), a live vaccine that is ingested instead of injected. The vaccine virus can mutate into a virulent form and result in rare cases of paralytic polio. For this reason, OPV is no longer used in the United States, and has been replaced on the Recommended Childhood Immunization Schedule by the inactivated polio vaccine (IPV).‘ College of Physicians, Philadelphia
‘Why must OPV vaccination be stopped? Vaccine-associated paralytic poliomyelitis was recognized shortly after the introduction of OPV, with cases occurring in both vaccines and their contacts. The time is coming when the only cause of polio is likely to be the vaccine used to prevent it. Ample molecular data are now available to demonstrate that vaccine viruses can revert to full neurovirulence.‘ Journal of Infectious Diseases
‘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
“Within a few years of the polio vaccine we started seeing some strange phenomena like the year before the first 300,000 doses were given in the United States childhood leukaemia had never struck in children under the age of two. One year after the first onslaught they had the first cases of children under the age of two that died of leukaemia…Dr Herbert Radnor observed that in a small area of this little town, in an area where no cases of leukaemia had been expected or at the most one in 4 years according to previous statistics, they suddenly had a rash like an epidemic within a few blocks.” Dr Eva Snead, author of ‘Some Call it Aids – I Call it Murder’
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). ‘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
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?
‘… failure to thoroughly investigate the increase in the incidence of non-polio acute flaccid paralysis (NPAFP) in areas where many doses of vaccine were used. NPAFP is clinically indistinguishable from polio paralysis but twice as deadly.’
‘…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.‘
‘Some mutations in polio viruses may be responsible for development of resistance to antibodies generated by OPV (Oral Polio Vaccine) and a reason for the recent steep rise in polio incidence since 2006. Because of these two factors, OPV cannot eradicate polio from India.’
‘Experts fear the disease could “come back with a vengeance”…polio is “at a tipping point”…initiative “now on an emergency footing”…strategy has been summarised as the “relentless pursuit of the unvaccinated child”.‘
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 immunization being conducted on the ground throughout India’s many provinces.
Year & corresponding AFP Cases reported (India): 2001 – 7470, 2002 – 9705, 2003 – 8508, 2004 – 13269, 2005 – 27049, 2006 – 32194, 2007 – 41524, 2008 – 45585, 2009 – 50405, 2010 – 55785, 2011 – 60754, 2012 – 60,792, 2013 – 54,639
Thus far this year (2014) incidence of Acute Flaccid Paralysis (AFP- ‘clinically indistinguishable from polio paralysis but twice as deadly’) in India is still spiking exponentially in direct proportion to the widespread Polio Mass Innoculation Program, currently at 34,025 cases – a conservative estimate. Meanwhile the WHO continues to maintain a case closed position on Polio in India, while systematically “discarding” the unprecedented surge in cases of Non-Polio Acute Flaccid Paralysis, in order to cover up their manifold criminal negligence.
Note: ‘All cases of AFP including Guillain-Barré syndrome, in children less than 15 years of age, or a patient of any age diagnosed as polio by a medical doctor must be regarded as possible polio cases until proven otherwise.‘…’Overall, the number of cases of polio in the (South-East Asia Region) Region has declined by more than 94%, from a reported 25 253 cases (Types 1, 2 and 3 *Wild Polio virus/WPV) in 1988 to 134 laboratory confirmed cases (Types 1 and 3 *Wild Polio virus/WPV) in only one country, India, in 2004. As of March 2006, India detected only 66 polio cases in 2005 compared to 134 in 2004.‘ WHO
‘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.
Two recent outbreaks in other countries were traced to India, where in the northern area as many as 75 percent of Muslim children under 2 have yet to receive polio vaccine, Dr. Aylward said. Although the polio extermination campaign reached 575 million children in 94 countries last year, Dr. Aylward said, there are geographic and worrisome demographic pockets of unvaccinated children like those in northern India. He also cited other geographic ”holes,” one around the Somali capital, Mogadishu, and another in eastern Angola, where conflicts had prevented comprehensive inoculation programs.’ New York Times, 2002
‘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
‘In 2007 number of (Polio/OPV) vaccination rounds were increased to one round every month, but in 2007 number of polio cases increased further. In 2005 there were 66 polio cases whereas in 2006 and 2007 number of polio cases increased to 676 and 863, respectively. Some mutations in polio viruses may be responsible for development of resistance to antibodies generated by OPV and a reason for the recent steep rise in polio incidence since 2006. Because of these two factors, OPV cannot eradicate polio from India.’ Maharaja Agrasen Hospital, Paediatrics, Vidhyadhar Nagar, Jaipur, India
‘India’s polio surveillance shows that the country is polio-free. But it also indicates that the country now has the world’s highest rate of non-polio AFP cases. According to data published in WHO’s Weekly Epidemiological Record, India’s annualised non-polio AFP rate for 2011 stood at 15.06 per one lakh children below 15 years of age, compared to a global rate that year of 5.48.
Moreover, most of the country’s non-polio AFP cases occur in just two States — Bihar and Uttar Pradesh. They accounted for about 61 per cent of the 53,000-odd non-polio AFP cases identified in the country in 2012, according to data from WHO’s National Polio Surveillance Project. As a result, the two States have far higher annualised non-polio AFP rates than other States — around 34 for Bihar and about 23 for Uttar Pradesh. The rate for the country as a whole is slightly over 12.
Children in Bihar and U.P. have received more doses of oral polio vaccine than elsewhere in the country. The oral vaccine, it was found, became less efficacious in the face of gut infections and diarrhoea that were widely prevalent in those States.
In their paper, Dr. Vashisht and Dr. Puliyel analysed the non-polio AFP rates across all States over 10 years up to 2010, and found that the rate “increased in proportion to the number of polio vaccine doses received in each area.” In 2012, the number of doses of oral vaccine given to children in Bihar and U.P. had come down and, for the first time, there was a decrease in the non-polio AFP cases in those States, Dr. Puliyel told this correspondent.‘ The Hindu/January 2013
‘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”.’
Eugenics Operation Tax shelter in action – ‘The single greatest threat to polio eradication is a funding gap, which Rotary is helping to address. Confident in Rotary’s commitment to the effort, the Bill & Melinda Gates Foundation awarded Rotary two grants totaling $355 million. Rotary’s US $200 Million Challenge, which runs through 30 June 2012, had raised $184 million as of 30 June 2011.’
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.
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.
‘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
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.’
‘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.
‘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
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.
We can now add Non-Polio Acute Flaccid Paralysis to that list. Thanks, in full, to the World Health Organization & Bill Gates.
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
VRM: Vaccine Clinic – A Concise Compendium To The Problem With Vaccines
VRM: The Problem With Vaccines Part 2 – Synergistic Effect of Heavy Metal Toxicity On The Body
VRM: The Problem With Vaccines Part 3 – Synthetic Genomics & The Death Of Natural Immunity
VRM: A Concise Compendium To The Problem With Vaccines Part 3 – Synthetic Genomics & The Death Of Natural Immunity
VRM: The Problem With Vaccines Part 4 – Primary Aspects of Vaccine Toxicity Affecting Body
VRM: The Problem With Vaccines Part 5A – Detoxification & Restoration of the Body
VRM: The Problem With Vaccines Part 5B – Detoxification & Restoration of the Body
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
VRM: Safe Alternatives to Vaccines
VRM: Family Charts Gradual Decline Of Daughter
VRM: Health Matters Part 1
VRM: Health Matters Part 2
VRM: Alternative Cancer Cures That Work
VRM: Pregnancy Tips
VRM: H1N1 Shot Reactions – Miscarriages
VRM: The Vanishing Sperm Count
VRM: H1N1 Vaccine Surplus From 2009 Reveals Growing Distrust of Gov’t & WHO
VRM: Flu Death Statistics – WHO & The Big Lie
VRM: Vaccine Industry Deception, Propaganda & Media Collusion
VRM: Birth of Medical & Scientific Dictatorship – Future Scenarios
VRM: H1N1 Bio-weaponry Incorporated
VRM: Aids & The WHO Connection – Criminal Intent
VRM: Morgellons Syndrome & Chemtrails
VRM: Council On Foreign Relations 10/16/09- Major Influence on Government Vaccine Policy
VRM: Closed Door CDC Meeting Reveals Industry Cover-up Of Heavy Metal Toxicity In Vaccines
VRM: The Rockefeller Foundation Drafts A Post-Pandemic Scenario
VRM: World Health Organization & Vaccine Manufacturers Implicated In Massive H1N1 Financial Scam Involving Kickbacks & Cover-ups
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.
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.
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.
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