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  • 5th July 2010 - By Joel Lord

    52592956CH008_Nigeria_BattlAccording to the World Health Organization vaccines aren’t to blame for the spread of Polio in Nigeria; but rather low vaccine uptake amongst the poorest communities. This despite the fact that, by their own admission, children receiving LIVE POLIO VIRUS DROPS will continue shedding the virus amongst their family & neighbors for weeks to come. 

    “At the main hospital in Mbarara during that month of 1977 more than 600 children died following polio vaccination.” United Nations

    The madness of “herd immunity”, the assumption that by vaccinating (infecting) everyone the herd will somehow maintain overall protection against life threatening diseases & viruses. This inverted logic serves only one agenda, that of a sustained Eugenics directive throughout the Third World. Since the introduction of this program Polio numbers have exploded in these isolated communities. The locals know full well it is Malaria (coupled with crippling poverty, a lack of proper sanitation & nutrition), NOT Polio which presents a genuine threat to their communities.

    The only solution – a radical upgrade of sanitation, hygiene & nutritional standards throughout these communities; not more mass vaccinations programs which spread otherwise dormant diseases to poor remote regions. You’ll never see the UN funding that type of a project in any Third World Nation. It would actually save lives & put them on a road to real long-term independence. Eugenics is always couched in “humanitarian” forms of deception.



    Mesothelioma (fatal tumor of the membrane surrounding the lungs), Brain cancers (Primarily Ependymomas & Choroid Plexus Tumors, but also Astrocytomas, Glioblastomas, Medulloblastoma, Meningiomas), Bone cancers (Primarily Osteosarcomas, but also Chondrosarcoma & Giant Cell Tumors), Post-Polio Syndrome, Chronic Fatigue Syndrome, Myalgic Encephalomyelitis, Aseptic Meningitis & Non-Hodgkin Lymphoma

    “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. When somebody gets malaria, if they have no money they even die. So the question I was asking and many people were asking was ‘If you really want to help children, why begin with a disease that they don’t have?”

    Mainstream Media selling UN Propaganda in support of Polio program:

    ‘A mutated virus from the oral vaccine used to prevent the spread of polio in Nigeria has paralyzed at least 124 children in the West African country this year. The new figure is double the 62 vaccine-derived cases reported in the country last year, and marks the continuation of the longest vaccine-derived polio outbreak ever seen, beginning in 2006, according to Oliver Rosenbauer, spokesman for World Health Organization’s Polio Eradication Initiative.

    The oral vaccine contains weakened live polio virus to build immunity in the patient, but can spread from a vaccinated person to the unvaccinated public and grow more virulent. If it is not contained and is allowed to mutate for months, it can grow strong enough to cause paralysis.

    “Where you get vaccine-derived cases is in communities where the routine vaccination is very low,” said Robert Scott, chair of the International PolioPlus Committee of the Rotary Foundation. Rotary International, the WHO, and the Centers for Disease Control and Prevention are part of a consortium of groups that support Nigeria’s immunization drive.

    “In this particular case in Nigeria, they stopped vaccinating for almost a year, so large areas were unvaccinated,” Scott said.

    Nigeria halted its polio vaccination program for more than a year in 2003 because of rumors the vaccine was a conspiracy against Muslims and that it caused infertility. With the encouragement of international health organizations, the country has worked to improve its coverage and implementation of polio vaccinations in recent years, but many remain unvaccinated.’

    WHO/CDC/UNICEF Initiative reveals their own hypocrisy & root cause of recent Polio outbreak: ‘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.

    “I was told by this preacher that when the government introduced the National Immunization Days in 1997, most of the children after vaccination started dying. The preacher told me that they had so much death that his cassock, that he wears to go and conduct the burial ceremony, got old. He said “I buried the children and my cassock got old.” In the same room there was one mother who had four children, and she hid one and took three other children for vaccination, and three children died and that one survived. Now when I went to do my presentation and I asked most of the people who were there – about two, three thousand people – each person had the same story.

    At the main hospital in Mbarara during that month of 1977 more than 600 children had died following polio vaccination. 600 children! So even some of the timid medical practitioners who were initially afraid to come out, started coming out giving information and saying ‘Oh, we knew this oral polio vaccine was trouble because as soon as the child receives it, they get a temper- ature and their health goes downhill and there is nothing that you could do.’ “—-Kihura Nkuba (Nov 2002)

    Money spent on vaccines when clean water and other diseases mostly ignored (45% of UNESCO funds is spent on vaccines):
    NB: 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. (Ref)

    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. When somebody gets malaria, if they have no money they even die. So the question I was asking and many people were asking was ‘If you really want to help children, why begin with a disease that they don’t have? (applause) Why not look for something that is killing them and save them from what is killing them ?’ And then (inaudible) ‘you know what, I like you very much. I save your children from this killer disease. Now there are no other diseases apart from this rare polio, so let’s go and fight that as well.’ But you don’t begin with the rarest disease and spend all the government’s meagre resources fighting polio, which is not a threat to most people, and then ignore something that is killing them in large numbers like malaria, like AIDS, like cholera, issues to do with sanitation, stunted growth – all the main things that matter to people the government was not fighting. Ugandan Kids Die By 1,000s —A Transcript of a talk given by Kihura Nkuba (Nov 2002) [emphasis added]

    “The forcing of them to take a vaccine 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. Uganda spent nine million of its meager resources marketing this European product (the money spent would have build 120,000 protected water springs giving 30% of the country access to clean water, it would have built ten ultra modern research centers looking at, for example, pests that are threatening the banana crop, but government chose European impose priorities.” “–Kihura Nkuba 2003

    “350 million Africans get malaria each year but do not appear to have the right to anti-malarial treatment. 2 million get TB annually yet AIDS spending is 90 times higher than TB spending and there is little left over for treating pneumonias, cancers, parasitics, bacterials or diabetes. What scientific or political justification could there be for this?”
    BMJ Rapid Response, 21 December 2003— Dr. John P. Heptonstall, MD, D.Ac., Director, Morley Acupuncture Clinic and Complementary Therapy Centre, Leeds, UK

    “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 (Nov 2002)

    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

    Polio Resurgence in Nigeria Traced to Mutating Vaccine

    Post Polio Syndrome

    UPDATE: The UN (Unicef) are continuing their misguided Polio program by reaching out to war ravaged communities in Iraq.

    polio3“The Salk vaccine failed completely. And the Sabin vaccine was a disaster. It caused many cases of polio and showed no relationship to the disease except for an increase in polio during the early ’60s, caused by the vaccine itself. And now we have the sensational findings from the Annals of the New York Academy of Sciences, which strongly indicate that polio did not go away at all, but now manifests itself as chronic fatigue syndrome.

    When the Coxsackie viruses were first isolated from CFS patients, it wasn’t realized that we were simply dealing with a new form of polio. This new polio was caused by the replacement of the polio viruses with their brothers, the Coxsackie viruses. As the researchers didn’t get the connection at first, these new polio cases were labled “post-polio syndrome,” “chronic fatigue syndrome,” and “myalgic encephalomyelitis.”” William Douglass MD

    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., F.C.C.P.

    ‘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

    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’

    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

    ‘Myalgic Encephalomyelitis (abbreviated ME) is a chronic, inflammatory, primarily neurological disease that is multisystemic, affecting the central nervous system (CNS), immune system and cardiovascular system, the endocrinological system and musculoskeletal system. ME can cause a wide variety of symptoms, including changes in sensory tolerance, visual problems, exertional muscle weakness, difficulties with coordination and speech, severe fatigability, cognitive impairment, problems with balance, subnormal or poor body temperature control (due to circulation issues) and severe pain. ME will cause a degree of impaired mobility and disability in all cases. The degree of impairment and complexity depends on the degree of diffuse brain injury and end organ involvement.

    Myalgic Encephalomyelitis affects the brain and spinal cord which control the body, allow thought and sensory processing, causing dysautonomia, impaired thinking and loss of internal homeostasis, the process whereby the body maintains a consistent internal environment in response to external stressors. Cellular metabolism and communication is disrupted, causing inefficiency in all biological processes. This includes the cellular mitochondria which process fuel to make energy, resulting in a deficiency of adenosine-triphosphate ATP with a chronic, severe, measurable loss of sustainable strength on exertion. A hallmark of ME is intolerance to previously trivial effort and deterioration through persistent or repeated exertion (often resulting in relapse).’

    New Controlled Study finds polyomavirus infection in postmortem brains of sufferers of Autism (inter-generational cross infection from Salk & Sabin Polio inoculations) – 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

    ‘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 Clinic Lerner College of Medicine;year=2008;volume=7;issue=1;spage=3;epage=3;aulast=Weiner


    ‘For four decades (currently five), government officials have insisted that there is no evidence the simian virus called SV40 is harmful to humans. But in recent years, dozens of scientific studies have found the virus in a steadily increasing number of rare brain, bone and lung-related tumors – the same malignant cancer SV40 causes in lab animals. Even more troubling, the virus has been detected in tumors removed from people never inoculated with the contaminated vaccine, leading some to worry that those infected by the vaccine might be spreading SV40.

    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.

    Researchers have several theories for how the virus could have spread from those infected through the Salk vaccine: in transmission from mother to fetus or through breast milk; through sexual activity or a flu-like virus.

    But the Lederle documents, which were obtained by Philadelphia attorney Stanley Kops in litigation not related to SV40, raise the possibility the virus might have been transmitted by contaminated oral vaccine, licensed for production in 1962.

    — A confidential memo in 1979 from a Lederle official stating: “It should be noted that Lederle did not test the original Sabin seeds for extraneous agents or neurovirulence since Dr. Sabin assured us that this had been done.”

    — Another memo stating that Lederle did not test the seed “since only 50 (milliliters) or less of each seed were provided by Dr. Sabin.”

    The two memos added that testing was unnecessary because later vaccine samples submitted for license were free of SV40.

    Kops also said that he had taken testimony in 1998 from a top Lederle official who said the company did not have the test results from many of the vaccine lots.

    “The vaccine manufacturers and the government need to disclose what really happened,” said Kops. “Without the facts, (scientists) will continue to look in the wrong places to explain how people were infected with SV40 after 1961.” Lederle did not respond to requests for comment.

    Last year (2000), a lawsuit was filed in Los Angeles against Lederle by the parents of 2 1/2-year-old Alexander Horwin who died of a brain tumor that later tested positive for SV40. The suit claims that the tumor was caused by SV40 and that he became infected through a 1997 oral polio vaccine.

    Kops and attorney Donald MacLachlin represent a New Jersey family that is considering a suit against vaccine manufacturers.

    In 1970, surgeons removed a large brain tumor from 2-year-old Mark Moreno. He since has undergone five more surgeries and now wears a protective helmet over the large opening in his cranium where bone grafts never took. Moreno, now 33, lives with his mother and requires daily assistance.

    Recent tests show Moreno’s tumor was riddled with SV40, according to the lawyers.

    Eileen Moreno, Mark’s mother, believes her son’s brain tumor was caused by SV40 and that he was infected through the oral polio vaccine in 1968.

    Last year (2000), two investigators from the U.S. Food and Drug Administration used genetic testing to examine 30 samples of bulk oral polio vaccine used in the United States going back to 1972. They reported finding no SV40. But the government has not used the genetic tests to determine whether vaccine made prior to 1972 was contaminated.

    Dr. William Egan, deputy director of the FDA’s vaccine research branch, said testing went back only to 1972 because those samples were the only ones available to them. “There was nothing sinister,” he said. MacLachlin said he finds it “incredible” that the government hasn’t comprehensively investigated the possibility of SV40 contamination of the oral vaccine. ‘

    ‘The virus has been detected in rare cancers, including:

    * Mesothelioma, a fatal tumor of the membrane surrounding the lungs. Few cases were reported prior to 1950, but the incidence has grown in the United States to 2,000 to 4,000 cases …a year, with greater incidence in Europe.
    * Brain cancers: Primarily ependymomas and choroid plexus tumors, but also astrocytomas, glioblastomas, medulloblastoma, and meningiomas. Fewer than 1, 000 cases of these cancers are reported in the United States each year.
    * Bone cancers: Primarily osteosarcomas, but also chondrosarcoma and giant cell tumors. These also make up fewer than 1,000 cases annually.’

    ‘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,” Carbone told the Vaccine Cell Substrate Conference 2004 in Rockville, Maryland, last week.

    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. The consequences of exposure to the virus (which is not related to HIV in any way) are unclear. There is evidence is that some of the people given contaminated vaccines were infected by SV40, and that such infections might lead to the development of certain rare types of cancer many years down the line. But the link with cancer has neither been proved, nor shown to be false.

    “There are two scenarios,” says Philip Minor of the National Institute for Biological Standards and Control in the UK. “One is that it doesn’t matter. The other is that it does.” Minor found three samples of the Soviet oral polio vaccine from the late 1960s in the NIBSC’s freezers, the only samples known to survive from this time. In 1999, he found they tested positive for SV40, whereas British samples from this period did not. “But we did not draw any broad conclusions,” Minor says.

    Now Carbone has carried out further tests. 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. In the third sample, there was no infectious poliovirus either, an indication that the sample of the live vaccine may have degraded.’


    ‘Health-care workers in Somalia today began a 3-day, United Nations-backed campaign to vaccinate more than 1.8 million young children against polio (2 nasal spray doses), 4 years after the Horn of Africa country was declared to be “polio-free”.’ “If we are to ensure that no new cases of polio emerge in Somalia, vaccination teams must be able to access every community, every household & every child aged under five.” Unicef Representative Rozanne Chorlton


    ‘Indian officials are firmly denying any causal link between the sudden death of an infant mere hours after receiving a 5th round dose of Polio Inoculation, part of an additional 2 round dosage of oral drops (Birth, 6 wks, 10 wks, 14 wks, 9-12 months, 18 moths, 2 yrs), despite conclusive evidence of viral shedding & paralytic poliomyelitis associated with the live virus Polio vaccine.  ‘The final postmortem report of a two-year-old boy who died hours after receiving oral polio vaccine has categorically established that the cause of death was not the vaccine.’

    Globalist funded Eugenics operation in Third World regions under fire as viral shedding from WHO conducted Polio mass vaccination program triggers an exponential spike in cases of paralysis (wild Polio strain variant) throughout India’s most heavily vaccinated communities – at least 47,500 cases of NPAFP (non Polio acute flaccid paralysis):

    ‘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’.

    January 12, 2012, marked a significant milestone for India as it was the first anniversary of the last reported wild polio case from India.

    The two doctors noted that it was long known to the scientific community that eradication of polio was impossible because scientists had synthesized poliovirus in a test-tube as early as in 2002. “The sequence of its genome is known and modern biotechnology allows it to be resurrected at any time in the lab,” they said and added, “Man can thus never let down his guard against poliovirus.”

    Dr Vashisht and Dr Puliyel said that another major ethical issue raised by the campaign is the 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.

    The authors noted that while India was polio-free in 2011, in the same year, there were 47500 cases of NPAFP. While data from India’s National Polio Surveillance Project showed NPAFP rate increased in proportion to the number of polio vaccine doses received, independent studies showed that children identified with NPAFP “were at more than twice the risk of dying than those with wild polio infection.”

    According to their report, nationally, the NPAFP rate is now twelve times higher than expected. In the states of Uttar Pradesh and Bihar — which have pulse polio rounds nearly every month–the NPAFP rate is 25 and 35 fold higher than the international norms.’

    Note: ‘… 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.’

    ‘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.’

    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.

    “Continuous maintenance of desired cold temperature during all the post manufacturing stages is known as cold chain. Oral polio vaccine (OPV) must be packed with dry ice (solid carbondioxide) during transportation and must be delivered at the point of use within three days. Even under freezing temperature conditions, the oral polio vaccine remains fluid as long as the temperature is above -140 C, due to the presence of sorbitol in the vaccine. The life period of OPV is one year after manufacture.

    While executing a pulse polio programme on a mass scale, some of the above mentioned vital cold chain precautions may not be strictly practiced. The reasons may be several such as ignorance, negligence, irresponsible or careless attitude, overload of work, tired and exhausted staff, routinisation of the process of programme implementation and lack of adequate supervisory control. If the sense of responsibility and accountability has not be inculcated, the desired goal of effective immunisation of every child will remain only a dream.

    Most of the lay people and dignitaries associated with the inauguration of the pulse polio programmes with fanfare in front of TV cameras are completely unaware of the technicalities involved in protecting the vaccine for guaranteed effectiveness. Even the two drops which are administered may not fall correctly in the mouth for proper swallowing by the child. Therefore, one major threat lurking constantly is the possible outbreak of polio infection, should the cold chain fail to work.

    It must be mentioned that some researchers have expressed doubts about the safety of oral polio vaccine. European countries such as Netherlands, Finland and Denmark so also USA have been advocating the use of intramuscular injectable polio vaccine, which contains killed virus. As long as the immunisation with live oral polio vaccine continues in our country, the risk of associated paralytic poliomyelitis will continue to threaten.” Dr WV Lawate, India.

    “Therefore, one major threat lurking constantly is the possible outbreak of polio infection…the risk of associated paralytic poliomyelitis will continue to threaten.” Dr. Salk

    “There must be some thing wrong with the polio drops if even after so many doses my child has contracted polio. The government should test medicines before they are used. Pata nahin bachchoo ko kya pila rahin hain!” (Don’t know what they are making my child drink), she adds.

    “Head of the pediatrics department of Delhi- based St Stephen’s Hospital, Jacob Puliyel, took up the matter with Lancet. In his strong-worded letter to Lancet’s editor, he wrote: “We are shocked and dismayed that Lancet should have published the paper on the protective efficacy of monovalent oral Type I poliovirus…having overlooked the serious ethical issues involved.” He went on to write, “What was introduced, according to this article, was a new vaccine that was five times more potent than previous vaccines, presumably also with the increased likelihood of adverse effects. No informed consent was taken, nor was the public told that the vaccine was experimental. Efforts were made to give the impression that the monovalent vaccine was not new.” – Tehelka (New Delhi, India),UNTESTED VACCINE SURFACES IN POLIO OUTBREAK, July 28, 2007

    “Using the unscientific rationale that “more is better” and with a callous disregard for human life and human rights, WHO officials replaced the tri-valent oral polio vaccine with an untested high potency monovalent Type 1 oral poliovirus vaccine without telling the public what it was doing. Now there is more Type 1 (and Type 2) polio in India plus an unexplained higher incidence of non- polio Acute Flaccid Paralysis following widespread use of the experimental polio vaccine.” Barbara Loe Fischer

    ‘A new weapon will now lead the country’s fight against polio. On Sunday, the government will launch a first-of-its-kind bivalent oral polio vaccine (BOPV), a single drop to protect against two deadly strains of polio presently existing in the country — P1 and P3.’ January 10, 2010′

    ‘Immunisation Schedule of Indian Medical Association re. OPV vaccinations:
    OPV – 7 doses (Birth, 6 wks, 10 wks, 14 wks, 9-12 months, 18 moths, 4-5 yrs).’

    ‘Polio eradication programme was launched in India in 1995, and polio eradication was expected to occur by 2000. Remarkable decline in polio incidence occurred, but, polio was not eradicated. Majority of polio cases are occurring in two states viz., Uttar Pradesh and Bihar. It is also being observed that majority of polio cases had received many doses of polio vaccine. In 2005 monovalent OPV1 (mOPV1) and monovalent OPV3 (mOPV3) were also introduced in Uttar Pradesh and Bihar, but, number of polio cases increased 10-fold in 2006. In 2007 number of 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 genetic factors in children from Uttar Pradesh and Bihar appear to be responsible for poor antibody generation by OPV. 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.’

    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?

    non-polio acute flaccid paralysis… 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.’

    non-polio acute flaccid paralysis 1Some 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.

    India has not reported any polio case since 13 January 2011 and has been removed from the list of endemic countries.‘ vs ‘60,754 total AFP (Non-Polio Acute Flaccid Paralysis) cases in 2011 (India).

    Note: ‘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”.

    Note: ‘ …incidence of NPAFP (Non-Polio Acute Flaccid Paralysis) was directly proportional to doses of oral polio received

    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 Second & Third World …while India was polio-free in 2011, in the same year, there were 47500 cases of NPAFP.‘; 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.
    Polio - triumphWhy 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 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 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.

    During 2011, incidence of Non-Polio Acute Flaccid Paralysis (‘clinically indistinguishable from polio paralysis but twice as deadly‘) 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” 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.

    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 correlation to the increased intensity of Polio immuniozation 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.

    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.‘ WHO

    WHO2Overall, 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.‘ World (Un)Health Organization

    ‘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.

    ‘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”.’

    ‘Every child during the first year of life should receive at least three routine doses of Oral Polio Vaccine (OVP). However, OPV is not 100 per cent effective. Even children who have received all routine doses and pulse polio doses can get the disease. The only way to completely eliminate the risk of getting children paralysed by polio is to completely interrupt the circulation of wild poliovirus by administration of OPV to all under-five children over a few days and repeat it a few times each year.’

    ‘The initial sites of polio virus replication are in monocytes and macrophages in the tonsils and the gut-associated lymphoid tissues (GALT), and subsequently in the gut epithelium and other lymphoid tissues. Neurons only become infected in 1–2% of individuals. The virus can infect these cell types because they express the polio virus receptor on their surface membranes. Most infected individuals develop no symptoms at all, but those who do generally experience a mild flu-like illness characteristic of an immune response against a viral infection, sometimes with gut associated symptoms such as nausea and vomiting. If the virus spreads to the central nervous system (CNS), there may be transient stiffness in the muscles.Infection of motor neurons in the spinal cord or brain stem can lead to cell death and acute flaccid paralysis (AFP) usually in the lower limbs, and less often to asphyxiation through paralysis of the respiratory muscles.’!via/oucontent/course/844/polio_case_study.pdf

    ‘bOPV >20% less immunogenic as mOPV1 for type 1; and as immunogenic as tOPV for type 3 or lower.’

    ‘Responses being explored include enhanced inactivated poliovirus vaccine (elPV) as a supplement to Oral Polio Vaccine(tOPV, mOPVI & mOPV3) and development of a bivalent OPV (bOPV) containing both type 1and type 3 virus  Panacea Biotec Ltd.’

    ‘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.

    ‘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).’

    ‘Salk cultured live Polio virus in diseased African Green Monkey kidneys (SV40 Patent). It was supposedly attenuated with formaldehyde & the heat treatment process to render the virus safe from harm. History has proven their method was far from foolproof as the virus component was not sufficiently “killed off”. Based on my understanding the problem was never fixed.

    ‘Some 50 to 65 monkeys will be used in a single morning. Under an anesthetic a surgeon removes the kidneys, after which the monkey is killed by an overdose of ether. Then the kidneys are cut into tiny pieces and placed in glass bottles with a special nutrient solution (No 199) devised by Dr. Salk. These bottles are then rocked in a mechanical machine for six days in an incubator to stimulate the growth of the kidney cells.

    At this stage fluid containing live polio virus is introduced and the bottles again rocked. After about four days the virus has multiplied a thousandfold in the kidney cells and is now chilled in 21 gallon bottles ready for transportation from Toronto to Eli Lilly & Co, and Parke, Davis & Co. There the brew is filtered free from the kidney cells (which might cause nephritis if injected into a human being) and diluted with formaldehyde to kill the virus.

    As we have already seen, there are three main strains of polio virus, against all of which there is need for protection. Consequently three tankfuls each containing one type of virus, cultivated and killed in the above manner, are mixed together. After neutralising the formaldehyde with sodium bisulphite there begins a month-long process of testing to see if the vaccine is safe for injection into human beings. This necessitates inoculations into live monkeys, rabbits, guinea-pigs and mice. These tests are carried out simultaneously, on each batch issued, by Dr. Salk’s laboratories and by the National Institute of Health at Bethesda, Maryland. Having passed the final tests the vaccine is distributed in little glass bottles for inoculation into children.

    The majority of the cases followed inoculation with the Cutter brand of the Salk vaccine, but the subsequent reports of laboratory tests were at first conflicting: The Minister of Health declared, in answer to a question in the House of Commons (June 17. 1955). that “No explanation for the Cutter vaccine incident has yet been found, but it is possible that certain batches contained live virus.” The Lancet (June 11, 1955. p. 1207) stated in a leading article that “the most likely explanation is that some of the vaccine contained live poliomyelitis virus which had not been completely inactivated by the formaldehyde treatment.” At any rate, in contrast to one report speaking of failure to isolate the virus from the Cutter vaccine- a purely negative laboratory result- –a more convincing report by Dr. Louis P. Gebhardt. Professor of bacteriology and Director of poliomyelitis Research Laboratory in the University of Utah, asserted that he had found live virus in samples of Cutter vaccine. This was confirmed by Dr. Scheele in a statement on television.

    The report issued by the United States Public health Service (Lancet, June I8, 1955) contains the definite statement, amidst much that is rather wordy, vague and technical, that during manufacture the formalin used for inactivation often failed to reach minute particles of live virus. This, together with several other circumstances connected with the development of the disease among the inoculated children, led them to conclude that the Cutter vaccine may have contained live virus. There can be little doubt that in fact it did.

    It was also revealed in this report that several of the six manufacturers licensed to make the Salk vaccine had the daunting experience of finding active virus-—in one instance in four out of six batches tested– –in the vaccine, when it should have been safe and ready for use.

    In the course of the investigations into the manufacture of the Cutter vaccine, it transpired that instead of tests being made upon every batch of vaccine before its issue, only “spot ” checks had been made. This would appear, face on the face of it, to be a most culpable omission amid one deserving the severest censure. At all events the experts of the United States Public Health Service, who carried out the inquiry into the manufacture, testing. and distribution of the cutter vaccine after this most humiliating fiasco that brought suffering and anxiety in millions of American homes insisted upon the application of most stringent safety measures before any more of this vaccine, and indeed of any of the various firms’ vaccines, could be issued for general use. Time (June 6, 1955) pungently commented: “The more the authorities congratulated themselves on the new tests, the more (by implication at least) did they condemn the old.”

    It is by no means reassuring to learn that Dr. Scheele, the American Surgeon General is reported in the New York Times (June 8. 1955) as telling the American Medical Association, at a meeting at Atlantic City, that the Salk vaccine is difficult to make and that no batch can ever be proved safe before it is given to children.

    The explanation of this somewhat startling pronouncement is to be found in a statement made by the city health commissioner of Milwaukee. Wisconsin, in May 1955, when referring to the safety tests made on monkeys. He said: ” Monkey tissues are not necessarily comparable to human tissues in this respect. This is exemplified by the fact that the amount of inactivated virus necessary to produce a good polio anti-body response in humans is far less than that needed in monkeys.” In other words the monkey is not so sensitive in the presence of virus as is the human being.

    Dr. Scheele also announced (Lancet. June 4, 1955) and the reader must do his best to reconcile the two statements–the safety of all Salk vaccines produced by the other American firms, and it was expected that the mass immunisation of children would begin again shortly. It had been the intention of the Government to inoculate 57 million people before August 1955.’

    ‘2002 Clinical Study verifies SV40/Cancer link – Association between simian virus 40 and non-Hodgkin lymphoma (Department of Medicine, Baylor College of Medicine, Houston, TX)

    FINDINGS: ‘Polyomavirus T antigen sequences, all of which were SV40-specific, were detected in 64 (42%) of 154 non-Hodgkin lymphomas, none of 186 non-malignant lymphoid samples, and none of 54 control cancers. This difference was similar for HIV-1-infected patients and HIV-1-uninfected patients alike. Few tumours were positive for both SV40 and Epstein-Barr virus. Human herpesvirus type 8 was not detected. SV40 sequences were found most frequently in diffuse large B-cell and follicular-type lymphomas.’

    INTERPRETATION: ‘SV40 is significantly associated with some types of non-Hodgkin lymphoma. These results add lymphomas to the types of human cancers associated with SV40.’

    Polio was on the decline well before the vaccine program was introduced. That quickly changed however with a rapid spike in numbers in 1954.

    ‘1954 Polio rate caused by the vaccine accelerates ten-fold in Massachusetts.

    1954 Eli Lilly company begins renovation of a five-story building in Indianapolis in July 1954 for the production of Salk vaccine. It is in full production by October of 1954. Wyeth, Parke-Davis and others follow suit.

    According to the ACS, they are predicting 6.4 million deaths from cancer, compared with 128,000 in 1933 – an increase of 6.2 million cases in 22 years. Vaccination, pesticide use and chemical pollution are the main factors that have increased since 1933.

    1955 Despite the skyrocketing cases of vaccine-induced polio, the AMA, NFIP and USPHS claim a reduction of 40-50%.

    1955 Idaho brings its Salk vaccination program to a halt on July 1, 1955. Utah does the same on July 12, 1955.

    1955 Vermont reports a 266% increase in polio since vaccinations began in 1954.

    1955 Rhode Island reports 454% increase in polio since vaccinations in 1954.

    1955 Massachusetts reports 642% increase in polio since vaccinations began in 1954 with vaccination of 130,000 children. In response, the National Foundation for Infantile Paralysis states that the increase in cases was due to the fact that “no children were vaccinated there.” Massachusetts bans the sale of Salk vaccine.”

    1955 Dr. Graham W. Wilson, director of Britains Public Health Laboratory Service, who knew about the NIH Salk vaccine trials, says “I do not see how any vaccine prepared by Salk’s method can be guaranteed safe.”

    1955 US Surgeon General Scheele admits in a closed session of the AMA that “Salk polio vaccine is hard to make and no batch can be proven safe before given to children”. Despite this fact, the public is told that the vaccine is safe. The government announces that it has the intention to vaccinate 57 million people before August 1955.’

    In 1977, Dr Jonas Salk who developed the first polio vaccine, testified along with other scientists, that mass inoculation against polio was the cause of most polio cases throughout the USA since 1961. (Science 4/4/77 “Abstracts” – Control of influenza and poliomyelitis with killed virus vaccines.) “Live virus vaccines against influenza and paralytic polio, for example, may in each instance cause the disease it is intended to prevent… Therefore, one major threat lurking constantly is the possible outbreak of polio infection…the risk of associated paralytic poliomyelitis will continue to threaten.” Dr. Salk” Dr. Jonas Salk testimony

    “Millions of people have been inoculated with anti-polio vaccine contaminated with tumoral SV40 virus (present in the green monkey cells ground to produce the vaccine). It is possible that it will take 20 or more years before the eventual harmful effects of the vaccine will manifest itself. ” Prof. Clausen, Director of the Institute of Preventative Medicine at the University of Odense, Denmark, 1/1/1973

    The United Nations, which overseas the World Health Organization (WHO), has been implicated in the promotion of live viruses & eugenics-type sterilization programs throughout the past, based on verifiable data.

    National Security Council Document 20506: Implications of Worldwide Population Growth for U.S. Security and Overseas Interests –

    ‘This 1974 memorandum drafted by Henry Kissinger led directly to the unleashing of experimental vaccines on the unsuspecting public. It sighted countries as targets for “initial population reduction experimentation to be implemented around the year 2000″. They identified India, Bangladesh, Pakistan, Nigeria, Mexico, Indonesia, Brazil, Philippines, Thailand, Egypt, Turkey, Ethiopia & Columbia for study. 3 million Filipinos ages 12-48 were given a test vaccine that ruined their health. North American Black & Native American Women were each given the same vaccine resulting in sterility rates of 25% & 35% respectively. The directive came from the WHO and was directly tied to Kissinger’s report.’

    It followed a 1972 report (Bulletin #47) issued by the World Health Organization which referred to an immune virus requested which would selectively destroy the Human T Cell System, to be distributed in conjunction with a Nationwide vaccination program “to observe the results”.

    Memoranda 47 – Virus-associated immunopathology: animal models and implications for human disease (Part 1)

    Memoranda 47 – Virus-associated immunopathology: animal models and implications for human disease (Part 2)

    This coincided precisely with the extensive Small Pox vaccination program in central Africa – shortly preceding the outbreak of Aids in Africa, America & elsewhere. The determining factor most common in Aids victims is the breakdown of the T Cell System in the body. Another coincidence.

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

    See VRM: Weaponized Polio & The African Green Monkey Conundrum

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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.

    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.

    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.


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