{"id":14588,"date":"2016-02-02T18:35:44","date_gmt":"2016-02-03T02:35:44","guid":{"rendered":"http:\/\/vaccineresistancemovement.org\/?p=14588"},"modified":"2016-08-08T18:20:22","modified_gmt":"2016-08-09T02:20:22","slug":"vrm-genetic-engineering-the-next-pandemic","status":"publish","type":"post","link":"https:\/\/vaccineresistancemovement.org\/?p=14588","title":{"rendered":"VRM: Genetic Engineering & The Next Pandemic"},"content":{"rendered":"
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“For decades, the disease transmitted by the Aedes genus of mosquito slumbered, affecting mainly monkeys. In humans, Zika occasionally caused a mild disease of low concern…The situation today is dramatically\u00a0different. Last year, the virus was detected in the Americas, where it is now spreading explosively. As of today, cases have been reported in 23 countries and territories in the region. The level of alarm is extremely high.<\/a>” <\/span><\/strong>World Health Organization Director-General Dr. Margaret Chan\u00a0<\/span><\/strong><\/div>\n
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Once again, the mainstream media vultures are purposefully exploiting the latest (potentially global) health crisis threatening our communities, with the stampeding Zika Virus, ramping up their rhetoric and fear-mongering headlines. <\/span><\/strong><\/div>\n
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The\u00a0origins, and the nature of this outbreak, an unprecedented spike in cases of microcephaly associated with symptoms of the strain, occurring mainly\u00a0in concentrated areas, seemingly without any environmental or biological catalyst, have left\u00a0the entire medical community scratching their heads.\u00a0<\/span><\/strong><\/div>\n
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So what is actually behind this multi-faceted mystery? The answers are to be found on the ground, in the heart of these impacted communities. You can be certain your Government Health Department has a vested interest in withholding the truth from ever\u00a0reaching the light of day. <\/span><\/strong><\/div>\n
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Given the implications, and the financial fallout, not to mention the impact on countless families a cover-up of this magnitude is having, and will have, for generations, who can blame them? We’re now entering uncharted territory. <\/span><\/strong><\/div>\n
\u00a0\"Zika<\/a><\/div>\n
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The Zika Virus (an RNA virus containing 10,794 nucleotides encoding 3,419 amino acids<\/a>) has long been considered a relatively innocuous, albeit contagious, localized pathogen, typically producing Flu-like symptoms in the host, on average subsiding within one to two weeks; certainly nothing on the scale comparatively, to that of the Dengue or Yellow Fever Virus variety, let alone Ebola<\/a> \u2013 each of which are associated with varying degrees of internal \u201cblackish\u201d bruising & widespread hemorrhaging (\u2018gastrointestinal bleeding, haematuria, skin petechiae, ecchymoses<\/a>\u2019) followed by rapid systemic deterioration, marked by Kidney failure, often leading to death.<\/strong><\/p>\n

\u2018Zika virus is an emerging mosquito-borne (Fla)virus that was first identified in Uganda in 1947 in rhesus monkeys through a monitoring network of sylvatic yellow fever. It was subsequently identified in humans in 1952 in Uganda and the United Republic of Tanzania. Outbreaks of Zika virus disease have been recorded in Africa, the Americas, Asia and the Pacific.<\/a>‘\u00a0<\/strong><\/p>\n

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‘Most reports describe a self-limiting febrile illness that could easily be mistaken for another arboviral infection, such as dengue or chikungunya fever.<\/a>` National Institutes of Health<\/strong><\/p>\n<\/div>\n

Symptomatology commonly associated with Zika Virus includes the following: <\/span><\/strong><\/div>\n
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\u2022<\/span>The incubation period ranges between approximately\u00a03 to 12 days after the bite of an infected mosquito.<\/span><\/a><\/strong><\/div>\n

\n\u2022Most of the infections remain asymptomatic (between 60 to 80%).<\/span><\/a>\u00a0<\/strong><\/div>\n

\n\u2022Disease symptoms are usually mild and the disease is usually characterised by a short-lasting self-limiting febrile illness of 4\u20137 days duration without severe complications, with no associated fatalities and a low hospitalisation rate.<\/span><\/a><\/strong><\/div>\n

\n\u2022The main symptoms are macular or papular rash, fever, arthralgia, non-purulent conjunctivitis\/conjunctival hyperaemia, myalgia and headache. The maculo-papular rash often starts on the face and then spreads throughout the body. Less frequently, retro-orbital pain and gastro-intestinal signs are present.<\/span><\/a><\/strong><\/div>\n
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However, until now, the epidemiology of Zika <\/strong><\/span>has demonstrated no consistent connection, whatsoever, to birth defects in humans.\u00a0Clearly,\u00a0some vital component must have\u00a0changed in the composition (nucleotide sequencing) of the virus, to render it more virulent; a sudden, dramatic shift in its response\/adaptability mechanism to the environment (or a marked deterioration in our capacity to respond\/adapt to\u00a0it), \u00a0by which to explain this\u00a0disturbing\u00a0anomaly. Notwithstanding those options, a rogue element would have to have been introduced in order to disturb the balance. <\/strong><\/span><\/div>\n
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The majority, if not all emerging viruses in the spectrum, have undergone so many changes, through decades of unmonitored l<\/strong>aboratory experimentation, re-engineering, chemical synthesis and genetic replication<\/strong><\/a> via vaccine programs (ie.<\/strong> Polio<\/strong><\/a>, <\/strong>MMR<\/strong><\/a>), <\/strong>they no longer resemble anything close to the naturally occurring, \u201cwild strains\u201d previously found in the environment.\u00a0 <\/strong><\/span><\/div>\n
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Science has proven that vaccines inhibit the immune response<\/a>, particularly in babies and young children<\/strong>, bypass\/breach their under-developed, naturally aligned defences <\/a>(80% of which are situated in the Mucosal membrane and the gastro-intestinal tract\/gut), attacking the newly formed primary core circuits – comprising the Blood-Brain barrier, Myelin sheath & Meninges<\/a>. The methodology, justifying vaccine uptake, is fundamentally flawed. <\/strong><\/span><\/div>\n
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\u201c<\/span><\/strong>But from all of the other studies of toxic substances, the earlier you work with the central nervous system, the more likely you are to run into a sensitive period for one of these effects, so that moving from one month or one day of birth to six months of birth changes enormously the potential for toxicity. There are just a host of neurodevelopmental data that would suggest that we\u2019ve got a serious problem. The earlier we go, the more serious the problem.<\/span><\/strong><\/a>\u201d Dr. Bill Weil\/Pediatrician, Academy of Pediatricians Committee on Environmental Health, CDC Simpsonwood Transcripts, 2000<\/span><\/strong><\/div>\n
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\"First<\/a><\/div>\n

How does this specific vulnerability to vaccines correlate with pregnant women?<\/strong><\/p>\n

Mother & child share the same immunity<\/a>\u00a0while the baby is \u2018In Utero\u2019 (all 3 trimesters);\u00a0including the entire duration of breast-feeding after birth. The Placenta and breast milk (Colostrum) are inextricably linked, providing a baby\u2019s primary initial source of nourishment through the long journey of formation in utero – while supplying the basic building blocks of life necessary to guarantee a safe transition into early childhood development.<\/strong><\/p>\n

Via this intrinsic lifeline, the fetus is also rendered highly susceptible to what\u00a0are termed\u00a0\u2018endogenous retroviruses’<\/a> (remnants of ancestral exogenous retroviral infections fixed in the germ-line DNA), passed on inter-generationally \u2013 primarily the result of previous exposure (grand-parent to parent to offspring) to the Polio, Tdap & MMR vaccines, from the mid 1950\u2019s through the late 1960\u2019s. The infant inherits any repository of cross-contaminated residue found in these shots, left embedded in the organs, bound to genetic material.<\/strong><\/p>\n

It goes without saying that pregnant women are at a heightened risk of adverse reactions to vaccines.<\/strong><\/p>\n

\u2018To address this serious situation (Microcephaly linked to Zika Virus), in late 2014, the Ministry of Health announced the introduction of the Tdap vaccine (comprising Diphtheria, Tetanus & Pertussis toxoids) for all pregnant women in Brazil.<\/a>‘<\/strong><\/p>\n

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Granted, any widespread immunization campaign targeting pregnant women which correlates with the epicenter of a sudden surge (mainly throughout sectors of north-eastern Brazil) is highly suspicious, given the verifiable track-record of serious adverse (auto-immune) reactions, neurological trauma and neuro-developmental difficulties, occurring in babies and young children following vaccination with Tdap<\/a>.<\/strong><\/p>\n

Surprisingly, in this instance, the timeline simply doesn\u2019t match up. Here is why.<\/strong><\/p>\n

First of all, the Tdap vaccine was not strictly enforced as a preventative measure for pregnant women, the key word being \u201crecommended<\/a>\u201d. Hence, the statistical\u00a0 numbers of those vaccinated women in this community cannot be fully verified.<\/strong><\/p>\n

More importantly, microcephaly has a unique signature which rules out any damage done beyond the second trimester.\u00a0<\/strong><\/p>\n

\u2018Microcephaly is a rare neurological condition in which an infant\u2019s head is significantly smaller than the heads of other children of the same age and sex. Sometimes detected at birth, microcephaly usually is the result of the brain developing abnormally in the womb or not growing as it should after birth.<\/a><\/strong><\/p>\n

Microcephaly can be caused by a variety of genetic and environmental factors. Children with microcephaly often have developmental issues. Generally there\u2019s no treatment for microcephaly, but early intervention with supportive therapies, such as speech and occupational therapies, may help enhance your child\u2019s development and improve quality of life.<\/a>‘ Mayo Clinic\u00a0<\/strong><\/p>\n

The brain and skull cavity develop throughout the first and second trimester. By 24 weeks gestation (in utero), the overall structure, mass & density of both areas has been firmly established.<\/strong><\/p>\n

‘The frontal bone, located superiorly and anteriorly on the skull, is the first of the cranial bones to begin ossification. The process begins to develop from two centers and is visible microscopically by alizarin-stain as early as 6-7 weeks gestation and radiographically by the 13th week.<\/a><\/strong><\/p>\n<\/div>\n

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There are two parietal bones located on each side of the brain, posteriorly to the frontal bone. The fetal parietals form from two centers of ossification that can be microscopically identified with alizarin-stain by 7-8 weeks gestation. Ossification of the two centers fuse quickly, forming an hour-glass shape in the early stages and rapidly develop into an ellipsoid recognizable by radiographic measures at around 20 weeks gestation. Although ossification and development begins at an early stage, the parietals are not identifiable by angles and borders until around the 24th week.<\/a>\u2019 Georgia State University, Department of Anthropology <\/strong><\/p>\n

\u2018<\/strong>The fifth week of pregnancy, or the third week after conception, marks the beginning of the embryonic period. This is when the baby\u2019s brain, spinal cord, heart and other organs begin to form.<\/strong><\/a><\/p>\n

Seven weeks into your pregnancy, or five weeks after conception, your baby\u2019s brain and face are rapidly developing.<\/a><\/strong><\/p>\n

By the 10th week of pregnancy, or eight weeks after conception, your baby\u2019s head has become more round.<\/a>\u2019 Mayo Clinic<\/strong><\/p>\n

\u2018The brain cells begin to divide at the tip of the embryo and form a tube. This neural tube then expands slowly to form the brain and the spinal cord. At first, the brain cells start to multiply quickly but the pace slows down during the second trimester.<\/a>‘ <\/strong><\/p>\n

Beyond that crucial second trimester window, any damage incurred there-after, ie. during the third trimester (from 27-38 weeks) will inevitably hinder early childhood development, but it cannot alter the basic physiology (proportions) of the brain & skull.<\/strong><\/p>\n

‘The most critical period for malformations and disruptions is the third to eighth week of gestation, during which the brain and most organs take form.<\/a>‘ Dimitri P. Agamanolis M.D.<\/strong><\/p>\n

\u2018<\/strong>It has been reported that in severe microcephaly the intracranial contents may not be visible sonographically, but this occurs only when the head is extremely small\u2026The available experience suggests that even expert ultrasound in pregnancies at risk will fail to diagnose fetal microcephaly in many cases. As most microcephalic infants have different types of cerebral maldevelopment, attention should be focused not only on the cranial measurements but on the cerebral anatomy as well.<\/strong><\/a>\u2018 Visual Encyclopedia of Ultrasound in Obstetrics and Gynecology<\/strong><\/p>\n

The Tdap vaccine is being administered to pregnant women during the third trimester only<\/a>. Therefore, based on these discrepancies,\u00a0 it must be ruled out of our investigation.<\/strong><\/p>\n

‘To maximize the maternal antibody response and passive antibody transfer to the infant, optimal timing for Tdap administration is between 27 and 36 weeks gestation (third trimester).<\/strong><\/a><\/strong>‘ Centers for Disease Control (CDC)\u00a0 <\/strong><\/p>\n

\u2018In order to optimize antibody transfer and protection at birth, taking into account the results from antibody kinetics studies performed in healthy adults, the recommendation is to vaccinate women between 28 and 38 weeks of gestation.<\/a>\u2019<\/strong><\/p>\n

\u2018Maternal immunization during the third trimester, immunization of other infant contacts, and reimmunization during subsequent pregnancies may be necessary.<\/a>‘ Infectious Disease Society of America, 02\/2013<\/strong><\/p>\n

Another red flag indicator of overlapping contradictions, those pregnant women who have given birth to babies with microcephaly, including their male counterpart in many instances, have traces of Zika virus showing up in their blood (male & female), semen (male) and breast milk (female).<\/strong><\/p>\n

\u2018Virus in blood, semen, milk in Brazil. 3 Dec 2015. FIOCRUZ detected presence of Zika virus in blood, semen and breast milk as announced by The Vice Director of Clinical Services of the National Institute of Infectious Diseases, Jose Serbino Neto.<\/a>‘ International Society for Infectious Diseases<\/strong><\/p>\n<\/div>\n<\/div>\n<\/div>\n

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This shifts the spotlight away from conventional vaccines, in identifying the key determining factor, toward another, more insidious source.<\/strong><\/p>\n

The only other rational, scientific-based explanation implicates mosquitos infected with the Zika Virus. And that is precisely where the primary evidence is pointing.<\/strong><\/p>\n<\/div>\n

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\"Aedes<\/a><\/div>\n
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\u2018The yellow fever mosquito, Aedes aegypti is a mosquito that can spread the dengue fever, chikungunya, Zika virus and yellow fever viruses, and other diseases. The mosquito is a small, dark mosquito of approximately 4 to 7 millimeters with typical white markings on the legs and a marking of the form of a lyre on the thorax. Females are larger than males, and can be distinguished by small palps tipped with silver or white scales.<\/a><\/strong><\/p>\n

In Zika virus infected mosquitos, the virus is present in the salivary glands of the mosquito. When a female Aedes aegypti bites a human for food, she injects saliva into the wound where the anti-coagulants contained in her saliva facilitate feeding. Since the virus can be passed from adult to egg, the virus is guaranteed to survive until the next summer and heavy rains.<\/a>‘ <\/strong><\/p>\n

The male variety of the Aedes aegypti mosquito, importantly, does not transmit disease directly to humans. His role is exclusively to mate with the female mosquito, impregnating as many as five\u00a0at a time<\/a> during his short lifespan, until he dies; typically after seven to eight\u00a0days<\/a>.<\/strong><\/p>\n

The female\u00a0(ectoparasite<\/a>), physically larger in size, is designed solely to reproduce, and, in order to ensure the survival of her eggs, upwards of \u00a0one to two hundred\u00a0per batch,<\/a> must acquire foreign blood, extracted from a mammalian (human) host, with which to see them through to \u201cmaturity\u201d.<\/strong><\/p>\n

\u2018The reason that (female) mosquitoes need to feed on our blood (containing proteins) is to reproduce. So the way that they find us is through olfaction (sense of odor\/smell). When mosquitos find us (via the carbon dioxide plume we emit) and bite us, or blood-feed from us, that is when they transmit infectious disease agents. So if we can prevent mosquitos from finding us, then we can prevent transmission of the diseases.<\/a>‘ National Institute for Allergy & Infectious Diseases<\/strong><\/p>\n

What is the vital connection between the Zika Virus contagion, the Aedes aegypti Mosquito, and ensuing cases of Microcephaly? Until now, the answers have been shrouded in conjecture, false leads and unsubstantiated data.<\/strong><\/p>\n

Back in 2011, when I completed \u2018VRM: The Problem With Vaccines Part 3 \u2013 Synthetic Genomics & The Death Of Natural Immunity’<\/span><\/a>, synthetic biology was still in its infancy.<\/strong><\/p>\n

The writing was on the wall, even then, sounding the alarm, as to the imminent risks posed by tampering with nature\u2019s delicate infrastructure, the imposition of transgenic organisms on a naturally evolving wild species.<\/strong><\/p>\n

Cutting edge, fly-by-night corporations are positioned to capitalize on a “wild west” of radical technological experimentation. Much like the corrupt vaccine industry, these white-collar criminal enterprises are also exempt from liability, or accountability.<\/strong><\/p>\n

We are told they are rendering a great service to society, the absence of which, our communities would be left at the mercy of nature`s cruel hand. But who is actually gambling with our lives here? Nature is not your adversary.<\/strong><\/p>\n<\/div>\n<\/div>\n<\/div>\n

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\u2018<\/span>Proponents of synthetic biology cite its potential to reduce our reliance on fossil fuels and transform medical care and human health, among other possible benefits. Critics express concerns about \u201cplaying God,\u201d threatening biodiversity and the organization and natural history of species, demeaning and disrespecting the meaning of life, and threatening longstanding concepts of nature. <\/span><\/a><\/strong><\/p>\n

First, sheer prudence suggests that we as a society must respect the intricacies of the natural world. Biological systems have developed over billions of years, and their interactions with the environment are astoundingly complex. We are far from being proficient speakers of the language of life, and our capacity to control synthetic organisms that we design and release into the world is promising but unproven.<\/span><\/a><\/strong><\/p>\n

Second, understanding our own limitations is an essential prelude to minimizing the risks that will accompany ongoing breakthroughs in synthetic biology and related fields. Like other new technologies, synthetic biology poses uncertain risks. Rapidity of change, both in the field of biology and in the public\u2019s understanding of it, as well as accelerating information exchange and technological competence heighten these concerns. Today, predicting cell function from gene sequence alone is very difficult and often impossible.<\/strong><\/span><\/a><\/p>\n

Among living beings, humans are in a unique position to be responsible stewards of nature, the\u00a0 earth\u2019s bounty, and the world\u2019s safety. Human society and governments have a duty to proceed prudently in promoting science and technologies, many of which can improve human welfare but also can harm the environment, create security risks, or otherwise lead to adverse consequences for vulnerable populations or future generations.<\/strong><\/span><\/a><\/p>\n

Benefits and risks extend to humans, nonhuman species, and the environment, each with unique needs and vulnerabilities. Emerging technologies present particularly profound challenges for responsible stewardship because our understanding of these potential benefits and risks is largely incomplete, preliminary, and uncertain. The prospect of intentional misuse by malicious actors further complicates efforts to respond adequately to the spectrum of benefits and risks.’<\/strong><\/a> <\/span>The Ethics of Synthetic Biology and Emerging Technologies\/Presidential Commission for the Study of Bioethical Issues, Washington, D.C., 2010<\/strong><\/p>\n

Note: ‘<\/strong>…our capacity to control synthetic organisms that we design and release into the world is promising but unproven.<\/a>‘<\/strong><\/span><\/p>\n

\u2018Some have advocated a total precautionary principle for genetic engineering, which means that no technology with any known risk should be attempted…Since no human action can be guaranteed to have zero risk, in practice, these principles are used to assess the relative safety of technology and are central to any public health program<\/span><\/a>.<\/span><\/a>‘ Discussion on the proposed hypothetical risks in relation to open field release of a self-limiting transgenic Aedes aegypti mosquito strains to combat dengue, Molecular Biotechnology, 05\/05\/2010<\/strong><\/p>\n

Fast forward to 2016. Brazil is currently ground zero for the most ambitious, cross-species genetic engineering experiment ever conducted on a human demographic.<\/strong><\/p>\n

Financed primarily with the support of a ‘$19.7 million grant from the Bill & Melinda Gates Foundation<\/span><\/a>‘ <\/span>Oxitec, a subsidiary of Intrexon Corporation,\u00a0a leader in synthetic biology<\/span><\/a><\/u>, quietly began testing a genetically engineered (GE) prototype mosquito, under the radar, as early as 2009.<\/strong><\/p>\n

\u2018Oxitec and its collaborators have performed open field release tests of Oxitec\u2019s Aedes aegypti (under permit from the regulators) in several countries (including the Cayman Islands, Malaysia and Brazil) from 2009.<\/span><\/strong><\/a>‘<\/p>\n

‘<\/span>Oxitec\u2019s mosquito, locally known as \u2018Friendly Aedes aegypti\u2019, is a revolutionary and environmentally sustainable tool that has already shown suppression of infestations of the wild Aedes aegypti mosquito, a goal which we\u2019ve been trying to achieve for many years in Brazil but haven\u2019t been able to. This solution is even more important today because beyond the dengue epidemic, we now have the Zika virus and chikungunya in Brazil,\u201d, <\/strong><\/a><\/span>\u00a0said Professor Wagner Pereira from Veiga de Almeida University.<\/a>‘<\/strong><\/p>\n<\/div>\n

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According to Oxitec’s strategy, the male Aedes aegypti mosquito, recognized as the courier\u00a0to the female, has been singled out, alterations made to its cellular structure, in an attempt to\u00a0disrupt\u00a0the lifecycle of the genus, to render the female sterile, and theoretically, to terminate any potential offspring which, according to company manuals, will ostensibly ‘<\/span>die before becoming functional adults.<\/span><\/a>‘<\/span><\/strong><\/div>\n
\"Mosquito-rearing\"<\/a><\/div>\n
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\u2018OX513A is a bisex RIDL (Release of Insects carrying a Dominant Lethal gene) strain. Males are released to mate with wild females. The progeny of such matings die as late larvae or pupae. Continual releases of sufficient numbers of RIDL males will reduce the target population to below the level needed to transmit disease. The late lethality means that RIDL larvae compete with wild-type larvae for resources, adding to the overall effectiveness of control.<\/a><\/strong><\/p>\n

Before release, male and female pupae are separated mechanically, exploiting the fact that they are naturally significantly different in size. The strain contains the DsRed marker which is clearly visible in larvae, a useful tool for quality control in production and effective monitoring in the field. OX513A is available in Asian and Latin American genetic backgrounds.\u2018<\/a><\/strong><\/p>\n

Despite bold predictions of success, and a relentless campaign endorsing the GE mosquito from Government Health departments, backed by mainstream media outlets,\u00a0 it was clear from the start that safety protocols had been bypassed altogether, legitimate field trial data white-washed and exaggerated, in an attempt to fast-track their technology into commercial production<\/a>.<\/strong><\/p>\n

\u2018However, no models of disease transmission appear to have been published by Oxitec or cited in the Risk Assessment. This is problematic because several authors have warned that a reduction in human immunity combined with residual disease transmission (from A. aegypti or A. albopictus) could result in a \u201crebound\u201d effect, in which the amount of serious disease increases, despite a reduction in the numbers of Aedes aegypti mosquitoes.<\/a>\u2018 GeneWatch UK<\/strong><\/p>\n

\u2018The National Technical Commission for Biosecurity (CTNBio), the collegiate body responsible for approval and regulation of transgenic organisms in Brazil, today approved the commercial release of the genetically modified (GM) mosquito, OX513A, developed by Oxitec.<\/a>‘<\/strong><\/p>\n

Take note of the date, May 15, 2014, which marked the start of a widespread release of transgenic mosquitoes into the environment.<\/strong><\/p>\n

Officially, <\/strong>field trials involving GE Mosquitos began in June of 2013, in the State of Bahia<\/strong><\/a>, Brazil; where two <\/strong>Microcephaly-related deaths<\/strong><\/a>\u00a0were later reported (December 2015).\u00a0 <\/strong><\/p>\n

\u2018The CTNBio (Brazil\u2019s National Technical Commission for Biosecurity) set a dangerous precedent by approving the commercial release of the (GE) mosquitoes before full epidemiological studies had been completed.<\/a>\u2019 Leonardo Melgarejo, Brazilian Ministry of Agrarian Development, and economist Antonio Inacio Andrioli, Regional Northwest University of Rio Grande do Sul in Brazil<\/strong><\/p>\n

\u201cIt is extraordinary that experiments with Oxitec\u2019s GM mosquitoes continue and commercial releases have even been approved without any monitoring of the effect on dengue.<\/a>\u201d Dr Helen Wallace, Director of GeneWatch UK<\/strong><\/p>\n

The first cluster of confirmed cases of Zika Virus in the epicenter region of Northeastern Brazil (Rio Grande do Norte) occurred in the early Spring of 2015.<\/strong><\/p>\n

‘First report of autochthonous transmission of Zika virus in Brazil: In the early (March) 2015, several cases of patients presenting symptoms of mild fever, rash, conjunctivitis and arthralgia were reported in the northeastern Brazil (21 acute-phase serum specimens from those patients exhibiting the “dengue-like syndrome).<\/a>‘<\/strong><\/p>\n

The index (first recorded) case in Brazil involving Zika Virus concomitantly with Microcephaly surfaced in November of 2015, in the State of Paraiba, which borders that of Rio Grande do Norte.\u00a0\u00a0\u00a0 <\/strong><\/p>\n

\u2018On 17 November, the Ministry of Health of Brazil reported the confirmation by RT-PCR, at the Flavivirus Laboratory at the Oswaldo Cruz Institute, of the presence of ZIKV RNA in amniotic fluid samples collected from two pregnant women with foetal microcephaly from the state of Para\u00edba.<\/a><\/strong><\/p>\n

Both pregnant women presented compatible symptoms of ZIKV infection during their pregnancy.<\/a><\/strong><\/p>\n

Based on the temporal correlation of these cases with the Zika epidemic, the health authorities of French Polynesia hypothesise that ZIKV infection may be associated with these abnormalities if mothers are infected during the first or second trimester of pregnancy.<\/a>‘ European Centre for Disease Prevention and Control, 11\/24\/2015<\/strong><\/p>\n

Logically, the mothers-to-be, in this instance, would have had to conceive by March of 2015, to given birth to their babies in November of the same year \u2013 ample opportunity for early (first trimester) exposure to the GE mosquito.<\/strong><\/p>\n

Note: \u201825 million transgenic insects were released between April and November<\/a>‘ of 2015. <\/strong><\/p>\n

Why was Oxitec so determined to avoid formal scrutiny? What were they hiding? <\/strong><\/p>\n

It turns out the formula behind the GE Mosquito, OX513A<\/span><\/a>, requires the use of an antibiotic, tetracycline hydrochloride (Sigma\u00ae): ‘Add a stock solution of tetracycline (3 mg\/ml in water – microgram per milliliter (\u00b5g\/ml)) to the trays at a 1:100 dilution to obtain the required final concentration of 30 \u00b5g\/ml.<\/span><\/a>‘<\/strong><\/p>\n

\u2018For rearing of the RIDL strain, 30 mg\/litre of tetracycline hydrochloride (Sigma\u00ae) was added to the rearing water, and to the 10% sugar water and blood offered to adults. Insectaries were maintained at 26\u00b0C (\u00b11\u00b0C) and 60% (\u00b110%) relative humidity with 12-hour light\/dark cycle.<\/a>\u2018 Oxitec Ltd.\u00a0 <\/strong><\/p>\n

‘Oxitec’s OX513A GM (genetically modified) mosquitoes have been engineered to be able to survive to adulthood only in the presence of tetracycline. The GM mosquitoes are bred to adulthood in the lab in the presence of the antibiotic…then released into the environment. The GM males are supposed to mate with wild females and their offspring are then supposed to die in the absence of tetracycline, mostly at the larval stage.<\/a><\/strong><\/p>\n

Oxitec’s “conditional lethality” trait is created by genetically engineering the mosquitos to express a protein called tTA (tetracycline-controlled transactivator). High level expression of tTA is toxic to the mosquitos and kills them at the larval stage, although the mechanism for this is not fully understood.<\/a>‘ Scientist Helen Wallace, Director of GeneWatch UK, excerpt from – Genetically Modified Mosquitoes: Ongoing Concerns<\/strong><\/p>\n

The goal is to outnumber & outsmart the natural selection process in the\u00a0Aedes aegypti Mosquito population, whereby the laboratory altered male will successfully mate with the wild female, and pass on the sterilizing tetracycline agent; to neutralize, ie. ensure the termination, of any offfspring (eggs). <\/strong><\/p>\n

“At the end of the day, It’s a numbers game. The more mosquitoes are out there, the more we release. We just need to outnumber the (wild) males….Each one of the (GE) males we release, die<\/a>.” Oxitec CEO Hadyn Parry<\/strong><\/p>\n

The antibiotic is expected to sustain the GE male mosquito just long enough to procreate. He then embeds the\u00a0antibiotic protein tTA\u00a0into the wild female, and apparently dies off thereafter. Any offspring, deprived of\u00a0Tetracycline at birth, will not survive past the larval stage of development – an altogether expensive & reckless theory, which has been vigorously challenged by numerous genetic engineering watchdog groups for its questionable scientific merits. <\/strong><\/p>\n

‘Oxitec has made misleading statements repeatedly in the media that its GM mosquitoes are sterile.<\/a>‘ GeneWatch UK Briefing, December 2010<\/strong><\/p>\n

‘This male is created by injecting very small amounts of synthetic DNA into thousands of mosquito eggs until finally one of the eggs accepts the DNA into its genome, creating two genes. One is a lethal gene, synthesized from E. coli and the herpes simplex virus. It’s lethal because it creates a protein called tTAV which interferes with a cell’s activity, killing the infected mosquito before it can reach adulthood…he’s also fed an antidote, tetracycline, as he’s being raised.<\/a>‘<\/strong><\/div>\n
\"Larvae<\/a><\/div>\n
Tetracycline is utilized in combination with E. coli bacteria laced with herpes simplex virus, ostensibly to ensure the male mosquito larvae reach the adult reproductive stage of development, before dying off. This strategy of interrupting the natural life-cycle via a witch’s brew of known toxins, will ultimately prove counter-intuitive to the natural laws of science, and devasting in its prolonged impact on the environment\u00a0\u00a0<\/strong><\/div>\n
<\/div>\n
“Every single one of these mosquitoes is going to die as larvae unless you go out of your way to save it. So you use tetracycline in the water to rescue that generation. Then that generation will grow to adults, they’ll lay more eggs, and the larvae would die, except you’ll feed them with some antidote, in which case they live again. So this is a fail-safe system for every generation.<\/a> ” Oxitec CEO Hadyn Parry <\/strong><\/div>\n
\"Tetracycline<\/a><\/div>\n

On its face, 30 \u00b5g\/ml (micrograms per millilitre) of tetracycline may not raise concern. After all, the product has been widely used on the market for decades, administered to treat acne and other bacterial infections; including applications in industrial agriculture<\/span><\/a>.<\/strong><\/p>\n

\u2018Tetracycline, is used to treat bacterial infections, including pneumonia and other respiratory tract infections; acne; infections of skin, genital and urinary systems; and the infection that causes stomach ulcers (Helicobacter pylori). It also may be used as an alternative to other medications for the treatment of Lyme disease and for the treatment and prevention of anthrax (after inhalational exposure). Tetracycline is in a class of medications called tetracycline antibiotics. It works by preventing the growth and spread of bacteria.<\/a>‘ Medlineplus<\/strong><\/p>\n

This prescription antibiotic is strictly meant to be taken orally, ‘comes as a capsule and suspension (liquid) to take by mouth’<\/span><\/a>, and is only ever injected for Veterinary purposes<\/span><\/a> (mainly cattle & horses). <\/strong><\/p>\n

\"Tetracycline<\/a><\/p>\n

A pregnant woman is highly vulnerable to drugs & antibiotics, particularly throughout the first trimester. Any minimal exposure is enough to seriously damage the fetus.<\/strong><\/p>\n<\/div>\n<\/div>\n<\/div>\n

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\u2018Tetracyclines have been shown to cross the placenta and may affect fetal bone formation<\/span><\/a>‘<\/strong><\/p>\n

\u2018Tetracycline has been assigned to pregnancy category D by the FDA. Animal studies have revealed evidence of embryotoxicity<\/span><\/a> (a substance that crosses the placental barrier; Injury to the embryo, which may result in death, growth retardation, or abnormal development of a part that may affect either its structure or function<\/span><\/a>)\u00a0\u00a0and teratogenicity\u00a0<\/strong><\/span><\/a>(developmental malformations<\/a><\/span>) <\/span><\/strong>ie<\/span><\/a>. birth defects, including toxic effects on skeletal formation<\/span><\/a><\/strong>.’ <\/span><\/strong><\/p>\n

‘There are no controlled data in human pregnancy, however, congenital defects and maternal hepatotoxicity have been reported. The use of tetracycline during pregnancy is generally not recommended, especially during the last half of pregnancy.<\/a><\/span><\/span>‘<\/strong><\/p>\n

Growth retardation, abnormal development, congenital defects, developmental malformations, toxic effects on skeletal formation, evidence of embryotoxicity: these are all textbook definitions of Microcephaly. <\/strong>Without a doubt, we have found our culprit. The clinical evidence is overwhelming. <\/strong><\/p>\n<\/div>\n

\n

Precisely how is tetracycline getting into the bloodstream of pregnant women?<\/strong><\/p>\n

Female mosquitoes are essentially the equivalent of flying vaccinators. The transgenic male, saturated in tetracycline solution, goes on to impregnate the wild female, cross-contaminating her system with the antibiotic, where-upon she transfers the toxic serum into the blood-stream of the awaiting human host; in this case, pregnant women.<\/strong><\/p>\n

Millions of voracious transgenic mosquitos are on the loose, jeopardizing the safety of\u00a0any pregnant woman, from exposure to multiple numbers of (cross-contaminated) female mosquito bites.<\/strong><\/p>\n

\u2018At the same time, many concerns have arisen about the risks of synthetic biology\u2026the release into the environment of novel, genetically modified organisms, either accidentally or deliberately (e.g., for bioremediation), potentially resulting in harmful consequences for ecological systems and\/or human health.<\/a>\u2019 ActionBioScience<\/strong><\/p>\n

\u2018Oxitec has played a key role in developing risk assessment processes for its own products and has omitted or downplayed some serious potential adverse effects of its technology in these risk assessment processes.<\/a>‘ GeneWatch UK\u00a0<\/strong><\/p>\n

It doesn\u2019t require a PhD in mathematics to recognize an imminent threat posed by this situation, if left unchecked \u2013 the accumulative effect, on fetal development, from prolonged tetracycline build-up in the bloodstream. For thousands of families, the real damage has already been done, and cannot be reversed.<\/strong><\/p>\n

Disturbingly, the synergistic effect of this unnatural collision of nature & technology has the potential to heighten the blood-seeking behavior of the female, including her ability to readily transmit the Zika Virus: \u2018Potential hazard SI No. (5): Wild females become aggressive after mating with GE sterile males. Increased biting activities (bloodmeal feasting on humans) and increased disease transmission (Zika Virus).<\/a>‘ <\/strong><\/p>\n

The long-term implications, in terms of the environmental impact, of introducing a laboratory-produced hybrid form of mosquito into an already fragile ecosystem, are unknown.<\/strong><\/p>\n

The long-term implications, in terms of the human cost, from a novel epidemic of this kind, impacting and altering our communities, are being completely ignored by health \u201cauthorities\u201d.\u00a0<\/strong><\/p>\n

The immediate consequences have been nothing short of disastrous.<\/strong><\/p>\n<\/div>\n

\n
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\"ZIka<\/a><\/div>\n
\n

Figures being reported are fluctuating daily, not surprisingly, given the general state of panic surrounding a crisis of this magnitude.\u00a0The Zika Virus scare\u00a0could turn out to be another overblown Pandemic<\/strong><\/a>, as we\u00a0endured\u00a0back in\u00a02009. It could also be far more serious than we recognize at this stage.\u00a0Caution and preparedness\u00a0for any contingency are\u00a0absolutely necessary.\u00a0<\/strong><\/strong><\/span><\/span><\/p>\n

‘Researchers have been looking at 4,180 suspected cases of microcephaly reported since October. On Wednesday (January 27, 2016), officials said they had done more intense analysis on more than 700 of those cases, confirming 270 cases and ruling out 462 others.<\/a>‘<\/strong><\/p>\n

One of the main reasons why statistical estimates on the number of cases of microcephaly have dropped, the criterion has recently been redefined. Many of those babies previously registered as having Microcephaly, showing a lesser reduction (circumference) in cranial size, have since been discounted.\u00a0\u00a0\u00a0\u00a0\u00a0 <\/strong>
\n\u00a0<\/strong>
\n‘As of 4 Dec 2015, the Brazil Ministry of Health has changed the criterion of microcephaly from 33 cm head circumference to 32 cm. This is expected to reduce the microcephaly case numbers considerably.<\/a>‘<\/strong><\/p>\n

‘The Oswaldo Cruz Hospital in Recife has become ground zero for fears over the Zika outbreak. On average the hospital now sees about 10 babies with microcephaly a day.<\/a>‘ 02\/01\/2016<\/strong><\/p>\n

Update: ‘Possible cases of microcephaly in Brazil have increased by six per cent in the last 10 days to 5,079 cases. Among them, 462 cases have been confirmed, 765 ruled out and the remaining 3,852 are still under investigation, the Ministry of Health said in a press release.<\/a>‘ 02\/13\/2016<\/strong><\/p>\n

‘I am now declaring that the recent cluster of microcephaly cases and other neurological disorders reported in Brazil, following a similar cluster in French Polynesia in 2014, constitutes a Public Health Emergency of International Concern.<\/a>‘ WHO Director-General summarizes the outcome of the Emergency Committee on Zika, 02\/01\/2016<\/strong><\/p>\n

The FDA has just approved the use of Genetically modified mosquitoes to combat Zika Virus spread in Florida. This will generate a plethora of irreversible consequences, with the introduction (conservatively) of tens of thousands of genetically engineered mosquitos into North America’s delicate ecosystem. <\/strong><\/div>\n
<\/div>\n
‘Oxitec Ltd. intends to ship eggs from the OX513A line of Ae. aegypti mosquitoes for a study in Key Haven, Monroe County, Florida. In conjunction with the FKMCD, Oxitec proposes to conduct an open field release trial for the OX513A Ae. aegypti male mosquitoes to determine whether such releases can reduce the population of local Ae. aegypti. Data collected during this study may be used in support of the New Animal Drug Application for this product.<\/a>‘ FDA Environmental Assessment for Investigational Use of Aedes aegypti OX513A\/August 05, 2016<\/strong><\/div>\n

\"Pyriproxyfen\"<\/a><\/p>\n

A team of doctors from the Faculty of Medicine, University of Buenos Aires,\u00a0 Argentina, have challenged the GE mosquito-Zika Virus-Microcephaly connection. They allege the use of a chemical larvicide, Pyroproxyfen, in high-density areas, is singularly to blame for the spike in cases of microcephaly.<\/strong><\/p>\n

‘Pyroproxyfen is applied directly by the Brazilian Ministry of Health on drinking-water reservoirs used by the people of Pernambuco, where the proliferation of the Aedes mosquito is very high (a situation similar to the Pacific Islands).This poison, recommended by the WHO, is a growth inhibitor of mosquito larvae, which alters the development process larva-pupa-adult, thus generating malformations in developing mosquitoes and causing their death or incapacity. It is analogous to the insect juvenile hormone or juvenoids, which has the effect of inhibiting the development of adult insect characteristics (for example wings, mature external genitalia) and the reproductive development, maintaining an “immature” aspect (nymph or larvae), which means that it acts by endocrine disruption and that is teratogenic.<\/a>‘<\/strong><\/p>\n

Note: ‘Malformations detected in thousands of children from pregnant women living in areas where the Brazilian state added pyriproxyfen to drinking water is not a coincidence, even though the Ministry of Health places a direct blame on Zika virus for this damage.<\/a>‘<\/strong><\/p>\n

Field trials<\/a> involving the larvicide, pyriproxyfen, currently being used to combat the Aedes aegypti mosquito population in Brazil, were conducted extensively during 2005-2006, in several concentrated regions (Malaysia. Peru & Cambodia<\/a>). <\/strong><\/p>\n

‘Trials were conducted in Malaysia against Ae. aegypti using 60 litre earthenware storage jars. To simulate actual usage 20% of the water was replaced every 2 weeks. Two dose rates of pyriproxyfen 0.5G were used – 0.01 mg\/l (0.01 ppm) and 0.02 mg\/l (0.02 ppm). Inhibition of emergence of adult mosquitoes was measured. Good control was achieved for 4 months at both dose rates. Additional tests with Aedes albopictus showed similar levels of efficacy.(Vythilingam et. al, 2005).\u00a0<\/a><\/strong><\/p>\n

A trial was conducted in Iquitos, Peru where 16 water tanks which actively supported breeding Ae. aegypti were selected. They were treated with doses of 50, 67 and 83 ppb pyriproxyfen. Samples of the water were taken back to the laboratory each month for 5 months where batches of 25 laboratory-reared fourth instar Ae. aegypti were added. Results demonstrate continued efficacy of pyriproxyfen over the 5 month trial period (Sichuincha et al.,2005).<\/a><\/strong><\/p>\n

Concrete domestic water storage jars are a common larval habitat for Ae. aegypti in Cambodia. Those used in these trials had a capacity of 200 litres.These jars were treated with pyriproxyfen 0.5 granules. Efficacy was good for up to 6 months with the higher dose rates inhibiting emergence of adult mosquitoes by >87% . At a dosage of 27 ppb pyriproxyfen, monthly removal and replacement of two thirds of the water did not reduce efficacy.’ (Chang Moh Seng et al., 2006).<\/a>‘\u00a0\u00a0<\/strong><\/p>\n

A\u00a0variation of\u00a0same product has been used for decades in California and elsewhere, as an environmental insecticide,\u00a0to mitigate loss in crop production.<\/strong><\/p>\n

‘Pyriproxyfen is a juvenile hormone mimicking insecticide, used for control of flies, beetles, midges and mosquitoes in public health applications. It is also used in agriculture in some countries, e.g. the USA.<\/a>‘ WHO<\/strong><\/p>\n

‘Currently, pyriproxyfen is used in California to control pests in apples, citrus, cotton, nuts, pears, and stone and pome fruits. In bait form, it is effective against the protein-feeding native southern fire ant (Solenopsis xyloni). An extensive resistance-management program has been developed for cotton that limits the number of applications of pyriproxyfen to one per growing season to reduce the rate of resistance development.<\/a>‘<\/strong><\/p>\n

If pyriproxyfen was responsible for the sudden unprecedented surge in cases of microcephaly on the ground in Brazil, then why did we not see similar outbreaks or clusters previously in Malaysia. Peru & Cambodia, let alone California?<\/strong><\/p>\n

There is already verifiable evidence linking the use of the antibiotic, tetracycline, as a sterilizing agent on Genetically Engineered mosquitos, with congenital malformations (teratogenicity).<\/strong><\/p>\n

There is no association between the application of pyriproxyfen in reservoirs, and the presence of the Zika Virus infection in the blood, semen & breast milk<\/a> of many of those couples whose child was born with microcephaly.<\/strong><\/p>\n

Clearly, pyriproxyfen is a toxic\u00a0substance that has irrevocably harmed the environment. However, speculation linking pyriproxyfen with Microcephaly is nothing short of speculative at this stage, because a connection cannot be verified without proper laboratory analysis – requiring blood samples taken from those women living in concentrated\u00a0areas affected; whose child was born with birth defects.<\/strong><\/p>\n

There is a plausible argument for cross-contamination of the reservoirs, supplying impoverished communities in north-eastern Brazil, compounded by the Aedes aegypti mosquito. Could pregnant women absorb enough pyriproxyfen to seriously damage the fetus? Without further testing and medical verification of concomitant factors, on a case-by-case basis, any such hypothesis must remain inconclusive.\u00a0This reinforces and confirms tetracycline as the main causal agent. <\/strong><\/p>\n

\"Brazil<\/a><\/p>\n

\n
\n
\n
\n

The genie is out of the bottle. Genetic engineering has unfortunately arrived, and begun to challenge nature in ways that no scientific analysis can determine. One thing is for certain, nature has proven, throughout history, a capacity to rebound against man\u2019s interventions. Rest assured, nature will respond to man\u2019s attempts at reshuffling the deck by literally re-assorting humankind.<\/strong><\/p>\n

We are witnessing the early stages of a nightmare scenario, unfolding before our eyes. This is a live field trial being conducted in real time, on an unsuspecting population. The problem now is, you can\u2019t turn back the clock.<\/strong><\/p>\n

\n

Millions of genetically engineered mosquitoes have already been released into the local environment, rendering any nation vulnerable to similar outbreaks on their own soil.<\/strong><\/p>\n

The survivability or adaptability of the GE mosquito, how its biochemistry reacts with other species, or replicates and spreads circulating viruses & bacterium, will ultimately depend on a myriad of unpredictable factors.<\/strong><\/p>\n

\"A<\/a>

A researcher at Rockefeller University feeds her stock of yellow fever mosquitoes.<\/p><\/div>\n

The stakes are high in Brazil, given the limitations posed by economic disparity in isolated rural communities, the fall-out from decades of Industrial waste, polluting of the soil & water-ways, coupled with insufficient hygiene, sanitation standards & nutrition brought on by poverty \u2013 a resulting dependency on and vulnerability toward government & World Health Organization sanctioned Health directives.<\/strong><\/p>\n

This is irrefutably a major crime against humanity. And yet, corporate malfeasance of this magnitude is commonplace in the Medical Industry, similar in scale to the watershed Thalidomide scandal<\/a> of the 1960\u2019s, yet far more concerning from a human perspective, given the potential for mutagenic shifts in viruses & bacterium exposed to transgenic technology, toward a far more virulent \u201cweaponized\u201d type of strain.<\/strong><\/p>\n<\/div>\n<\/div>\n

\n
\n
\n

Eventually, corporations such as Oxitec are held accountable for their gross misconduct, as countless families, impacted by these reckless, profit-making schemes, band together as one, organize class action lawsuits, and speak out in public. <\/strong>Financial liability simply doesn\u2019t constitute justice served, given the suffering incurred within these families. <\/strong><\/p>\n

Beyond the devastating daily reality posed by Microcephaly, as innocent children are being stripped of a normal life at birth, there is a hidden legacy of social stigma and inward shame many parents will have to endure in silence.<\/strong><\/p>\n

Families are fed up. Something has to be done now to stop this cycle of abuse. It is our responsibility as concerned citizens, proactive parents and critically- thinking individuals, to become educated on these clear and present dangers to our health, to encourage safe, viable alternatives to western Allopathic methods & Medical Industry propaganda, and to resist government wrong-doings without fear of retribution.<\/strong><\/p>\n

After all, elected representatives green-lighted nothing short of a Frankenstein experiment on their own people, without any oversight or precautionary measures; and have thus, inadvertently placed the health & safety of the entire global community at risk.\u00a0<\/strong><\/p>\n

Given enough resources, this misguided Industry will eventually have the ability, and the authority, to re-engineer our entire species, in fact, any species, at will. The whole issue of genetic engineering, the immersion of transgenic organisms into the environment, needs to be front & center on the political radar. We don\u2019t have a generation to observe the results. It\u2019s time to take a stand now, to do your share, while we still can, and make an impact on humanity\u2019s course of action.<\/strong><\/p>\n

Ask yourself, where has our systemic, blind faith in outside forces gotten us thus far? The question is, what are you prepared to do about it? Fortunately, the solution is within your reach. Knowledge is much stronger than tyranny. And in the end, the truth is stronger than lies. Our children deserve the right to a brighter future, and we must, accordingly, lead by example. <\/strong><\/p>\n<\/div>\n

See: VRM: Ebola Report<\/a><\/strong><\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n

\n

See: VRM: Measles Report <\/a><\/strong><\/p>\n

See: VRM: Vaccines Do Contain Aborted Human Fetal Tissue<\/a><\/strong><\/p>\n

See: VRM: The Rise of Mutagenic Viruses<\/a><\/strong><\/p>\n

VRM: The Autism Report http:\/\/vaccineresistancemovement.org\/?p=10185<\/a><\/strong><\/p>\n

VRM: Worldwide Autism Study Direct link to study: http:\/\/study.vaccineresistancemovement.org\/<\/a><\/strong><\/p>\n

VRM: The Problem With Vaccines Part 1 http:\/\/vaccineresistancemovement.org\/?p=488<\/a><\/strong><\/p>\n

VRM: Vaccine Clinic \u2013 A Concise Compendium To The Problem With Vaccines<\/strong>http:\/\/vaccineresistancemovement.org\/?p=6278<\/a><\/strong><\/p>\n

VRM: The Problem With Vaccines Part 2 \u2013 Synergistic Effect of Heavy Metal Toxicity On The Body http:\/\/vaccineresistancemovement.org\/?p=6097<\/a><\/strong><\/p>\n

VRM: The Problem With Vaccines Part 3 \u2013 Synthetic Genomics & The Death Of Natural Immunity http:\/\/vaccineresistancemovement.org\/?p=6880<\/a><\/strong><\/p>\n

VRM: A Concise Compendium To The Problem With Vaccines Part 3 \u2013 Synthetic Genomics & The Death Of Natural Immunity http:\/\/vaccineresistancemovement.org\/?p=7283<\/a><\/strong><\/p>\n

VRM: The Problem With Vaccines Part 4 \u2013 Primary Aspects of Vaccine Toxicity Affecting Body http:\/\/vaccineresistancemovement.org\/?p=8787<\/a><\/strong><\/p>\n

VRM: The Problem With Vaccines Part 5A \u2013 Detoxification & Restoration of the Body http:\/\/vaccineresistancemovement.org\/?p=8836<\/a><\/strong><\/p>\n

VRM: The Problem With Vaccines Part 5B \u2013 Detoxification & Restoration of the Body http:\/\/vaccineresistancemovement.org\/?p=8847<\/a><\/strong><\/p>\n

VRM: PCV Vaccine Exposed \u2013 Breeding Ground For Staphylococcus Aureus http:\/\/vaccineresistancemovement.org\/?p=9431<\/a><\/strong><\/p>\n

VRM: Pandemic Preparedness & The Dark Agenda Ahead http:\/\/vaccineresistancemovement.org\/?p=9460<\/a><\/strong><\/p>\n

VRM: Polio \u2013 United Nations & The Great Cull http:\/\/vaccineresistancemovement.org\/?p=4916<\/a><\/strong><\/p>\n

VRM: The Re-emergence of Polio in The Third World (compliments of the World Health Organization & Bill Gates) http:\/\/vaccineresistancemovement.org\/?p=10091<\/a><\/strong><\/p>\n

VRM: Weaponized Polio & The African Green Monkey Conundrum <\/strong>http:\/\/vaccineresistancemovement.org\/?p=10727<\/a><\/strong><\/p>\n

VRM: Mandatory Vaccinations \u2013 How They Will Be Implemented http:\/\/vaccineresistancemovement.org\/?p=11806<\/a><\/strong><\/p>\n

VRM: The Confidential Case-files of GlaxoSmithKline \u2013 Cover-up, Deferral & Denial of Responsibility for Vaccine-related Premature Deaths http:\/\/vaccineresistancemovement.org\/?p=12242<\/a><\/strong><\/p>\n

VRM: Primary Reasons Not To Get The Flu Shot http:\/\/vaccineresistancemovement.org\/?p=12642<\/a><\/strong><\/p>\n

VRM: The Flu Report http:\/\/vaccineresistancemovement.org\/?p=9226<\/a><\/strong><\/p>\n

VRM: Vaccine Ingredients http:\/\/vaccineresistancemovement.org\/?p=979<\/a><\/strong><\/p>\n

VRM: Safe Alternatives to Vaccines<\/strong>http:\/\/vaccineresistancemovement.org\/?p=662%EF%BB%BF<\/a><\/strong><\/p>\n

VRM: Family Charts Gradual Decline Of Daughter http:\/\/vaccineresistancemovement.org\/?p=3156<\/a><\/strong><\/p>\n

VRM: Health Matters Part 1 http:\/\/vaccineresistancemovement.org\/?p=6719<\/a><\/strong><\/p>\n

VRM: Health Matters Part 2<\/strong>http:\/\/vaccineresistancemovement.org\/?p=6746%EF%BB%BF<\/a><\/strong><\/p>\n

VRM: Alternative Cancer Cures That Work http:\/\/vaccineresistancemovement.org\/?p=3729<\/a><\/strong><\/p>\n

VRM: Pregnancy Tips<\/strong>http:\/\/vaccineresistancemovement.org\/?p=3270<\/a> <\/strong><\/p>\n

VRM: H1N1 Shot Reactions \u2013 Miscarriages http:\/\/vaccineresistancemovement.org\/?p=943<\/a><\/strong><\/p>\n

VRM: The Vanishing Sperm Count http:\/\/vaccineresistancemovement.org\/?p=4639<\/a><\/strong><\/p>\n

VRM: H1N1 Vaccine Surplus From 2009 Reveals Growing Distrust of Gov\u2019t & WHO http:\/\/vaccineresistancemovement.org\/?p=4969<\/a><\/strong><\/p>\n

VRM: Flu Death Statistics \u2013 WHO & The Big Lie http:\/\/vaccineresistancemovement.org\/?p=784<\/a><\/strong><\/p>\n

VRM: Vaccine Industry Deception, Propaganda & Media Collusion<\/strong>http:\/\/vaccineresistancemovement.org\/?p=197<\/a><\/strong><\/p>\n

VRM: Birth of Medical & Scientific Dictatorship \u2013 Future Scenarios http:\/\/vaccineresistancemovement.org\/?p=997<\/a><\/strong><\/p>\n

VRM: H1N1 Bio-weaponry Incorporated http:\/\/vaccineresistancemovement.org\/?p=884<\/a><\/strong><\/p>\n

VRM: Aids & The WHO Connection \u2013 Criminal Intent<\/strong>http:\/\/vaccineresistancemovement.org\/?p=1749<\/a><\/strong><\/p>\n

VRM: Morgellons Syndrome & Chemtrails http:\/\/vaccineresistancemovement.org\/?p=839<\/a><\/strong><\/p>\n

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

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

VRM: The Rockefeller Foundation Drafts A Post-Pandemic Scenario http:\/\/vaccineresistancemovement.org\/?p=5102<\/a><\/strong><\/p>\n

VRM: World Health Organization & Vaccine Manufacturers\u00a0Implicated In Massive H1N1 Financial Scam Involving Kickbacks &\u00a0Cover-ups<\/strong>http:\/\/vaccineresistancemovement.org\/?p=4610<\/a><\/strong><\/p>\n

VRM Live \u2013 01\/28\/11: Vaccine Resistance Movement founder Joel\u00a0Lord\u00a0discusses Synthetic Genomics, cloned cell vaccine technology\u00a0& the\u00a0death of natural immunity, gutter journalism & Dr.\u00a0Wakefield\u2019s\u00a0imminent vindication with \u2018Truth to Power\u2019 host Paul Mabelis. http:\/\/www.blogtalkradio.com\/empradio\/2011\/01\/28\/truth-to-power-thursday<\/a><\/strong><\/p>\n

VRM Live <\/strong>\u2013 11\/04\/10<\/strong>: <\/strong>Vaccine\u00a0Resistance Movement founder Joel Lord lays out the whole vaccine\u00a0process\u00a0with Paul Mabelis; including heavy metal toxicity, synergy, pregnancy issues & the basic principles of natural health at risk. http:\/\/www.blogtalkradio.com\/show.aspx?userurl=empradio&year=2010&month=11&day=05&url=truth-to-power-thursday<\/a><\/strong><\/p>\n

VRM Live <\/strong>\u2013 09\/24\/10<\/strong>:\u00a0Vaccine\u00a0Resistance Movement Founder Joel Lord & activist\/radio host Jesse\u00a0Calhoun lay it all out tonite. Topics include the VRM\u00a0Worldwide Autism Study, <\/strong>Scientific\/Medical\u00a0dictatorship, Natural Rights & Vaccine Industry fraud exposed. Special thanks to host Paul Mabelis. http:\/\/www.blogtalkradio.com\/empradio\/2010\/09\/24\/truth-to-power-thursday<\/a><\/strong><\/p>\n

If you appreciate the efforts to bring this information\u00a0forward\u00a0 do consider making a donation. Any amount, no matter how small\u00a0\u00a0 will\u00a0 help enable me to carry on this invaluable research. See Paypal link\u00a0on the VRM website <\/strong>(click on \u2018Donate\u2019 tab in upper right corner)<\/strong><\/strong><\/strong><\/strong><\/strong>. Thank you all. <\/strong><\/p>\n

\"logo.VRM_Ver.2.1\"<\/a><\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"

“For decades, the disease transmitted by the Aedes genus of mosquito slumbered, affecting mainly monkeys. In humans, Zika occasionally caused a mild disease of low concern…The situation today is dramatically\u00a0different. Last year, the virus was detected in the Americas, where it is now spreading explosively. As of today, cases have been reported in 23 countries […]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[231],"tags":[],"class_list":["post-14588","post","type-post","status-publish","format-standard","hentry","category-vrm-genetic-engineering-the-next-pandemic"],"_links":{"self":[{"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=\/wp\/v2\/posts\/14588","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=14588"}],"version-history":[{"count":152,"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=\/wp\/v2\/posts\/14588\/revisions"}],"predecessor-version":[{"id":15105,"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=\/wp\/v2\/posts\/14588\/revisions\/15105"}],"wp:attachment":[{"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=14588"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=14588"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=14588"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}