{"id":10934,"date":"2012-09-24T20:25:07","date_gmt":"2012-09-25T04:25:07","guid":{"rendered":"http:\/\/vaccineresistancemovement.org\/?page_id=10934"},"modified":"2014-04-19T12:29:26","modified_gmt":"2014-04-19T20:29:26","slug":"vrm-wire14","status":"publish","type":"page","link":"https:\/\/vaccineresistancemovement.org\/?page_id=10934","title":{"rendered":"VRM Wire14"},"content":{"rendered":"

Breaking News:<\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong>\u00a0The vanguard of\u00a0current Influenza Vaccine formulations are utilizing cloned (chemically synthesized & replicated in a laboratory) insect-virus vectors in which to harness the Influenza viruses for mass production. No matter which route you take in terms of the application of 21st century vaccine production technology (cloning), all roads will inevitably lead to otherwise avoidable forms of hybrid cancer<\/span><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/span><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/span><\/strong><\/strong><\/p>\n

\"\"<\/a><\/span><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/span><\/strong><\/strong><\/p>\n

It should come as no surprise that the flagship model, the first major Cloned cell-based vaccine ever for mass production, FLUVIRIN\u00ae, manufactured by Novartis Vaccines, was introduced in the Fall of 2011 in the United States with the annual Flu shot; touted as a \u2018Recombinant Trivalent Hemagglutinin Protein-based Influenza Vaccine<\/a>‘. ‘As soon as the influenza vaccine strains are selected, the genes encoding the HA proteins are cloned into baculovirus vectors. Insect cells infected with these vectors express HA (Hemagglutinin) proteins, which are then further purified and formulated into a trivalent vaccine (assortment of 3 viruses).\u2019<\/strong><\/div>\n

Note: Package Insert – ‘FLUVIRIN\u00ae has been standardized according to USPHS requirements for the 2012-2013 influenza season and is formulated to contain 45 mcg hemagglutinin (HA) per 0.5-mL dose in the recommended ratio of 15 mcg HA of each of the following 3 viruses: A\/Christchurch\/16\/2010, NIB-74 (H1N1) (an A\/California\/7\/2009-like virus); A\/Victoria\/361\/2011, IVR-165 (H3N2); and B\/ Hubei-Wujiagang\/158\/2009, NYMC BX-39 (a B\/Wisconsin\/1\/2010-like virus). The 5-mL multidose vial formulation contains thimerosal, a mercury derivative, added as a preservative. Each 0.5-mL dose from the multidose vial contains 25 mcg mercury.’<\/a><\/strong><\/p>\n

Novartis Vaccines & Diagnostics has been awarded a $487 million contract by the US Dep\u2019t of Health & Human Services, with federal funds coming from the Biomedical Advanced Research and Development Authority (BARDA), a joint venture totalling nearly $1 billion US in investment<\/a>, to produce \u201850 million doses of seasonal trivalent flu vaccine, and up to 150m doses of monovalent vaccine<\/a>‘ in preparation for a potential Pandemic.<\/strong><\/p>\n

‘If a flu pandemic strikes the United States, a Novartis\u00a0 (NYSE: NVS<\/a> )\u00a0 plant in North Carolina now stands ready to respond with vaccine techniques that offer speed and scalability advantages over traditional<\/a> vaccine-making methods. Novartis’ vaccine facility in Holly Springs, North Carolina today became the first cell culture vaccine facility authorized by the U.S. Food and Drug Administration<\/a> for emergency use during a pandemic. The plant will develop vaccines from cultured animal cells, in contrast to the traditional method of making flu vaccines from chicken eggs. The Novartis site is designed to provide 150 million adjuvanted doses of pandemic influenza vaccine within six months of declaration of an influenza pandemic. In the event of an influenza pandemic, the new Novartis facility could produce up to 25 percent of the vaccine needed in the United States.’ 12\/13\/11<\/strong><\/p>\n

Barda is leveraging its options in this highly lucrative \u201cmarketplace<\/a>\u201c, by simultaneously finacing the competition. One such manufacturer entering the arena, Protein Sciences Corporation (PSC), with the help of a $147 million joint contribution (\u2018awarded a contract in June 2009 to support further development and scale-up of our flu vaccines, FluBlok and PanBlok\u2019<\/a>), have launched a major campain to unseat Novartis, with their very own misguided cloning-type patent for vaccine production, involing the replication of \u201ctransgenic insect cells\u201d for use in vaccine production. \u2018We have established a broad patent estate on influenza vaccines produced using recombinant technology in our expresSF+ cells.<\/a>‘<\/strong><\/div>\n
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\"\"<\/a>ExpresSF+ Cells Patent \u2018Baculovirus-based vectors have been generated (or can be generated without undue experimentation) that allow the cloning of large numbers of inserts, at any of a variety of cloning sites in the viral vector. Thus, more than one heterologous polypeptide may be introduced together into a transgenic insect cell or insect of the invention. The viral vector can be introduced into an insect cell or insect by conventional methods, such as by in vitro inoculation (insect cells) or oral ingestion (insect larvae).\u2019<\/a><\/strong><\/p>\n

1. ‘As soon as the influenza vaccine strains are selected, the genes encoding the HA proteins are cloned into baculovirus vectors. Insect cells infected with these vectors express HA (Hemagglutinin) proteins, which are then further purified and formulated into a trivalent vaccine (assortment of 3 viruses).\u2019<\/a> New England Journal of Medicine – relating to the Novartis Vaccine formula<\/strong><\/div>\n
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2. \u2018Baculovirus-based vectors have been generated (or can be generated without undue experimentation) that allow the cloning of large numbers of inserts<\/a>‘ Protein Sciences Corporation<\/strong><\/div>\n

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Excerpt from VRM: The Problem With Vaccines Part 3 \u2013 Synthetic Genomics & The Death Of Natural Immunity<\/a><\/strong><\/div>\n

\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014<\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/span><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/span><\/strong><\/strong><\/p>\n

Breaking News: Study Links Thimerosal Use in Vaccines with Premature Cell Death & Mitochondrial Disfunction\u00a0 <\/span><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/span><\/strong><\/strong><\/p>\n

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Thimerosal-Derived Ethylmercury Is a Mitochondrial Toxin in Human Astrocytes – Possible Role of Fenton Chemistry in the Oxidation and Breakage of mtDNA: ‘Thimerosal generates ethylmercury in aqueous solution and is widely used as preservative. We have investigated the toxicology of Thimerosal in normal human astrocytes, paying particular attention to mitochondrial function and the generation of specific oxidants. We find that ethylmercury not only inhibits mitochondrial respiration leading to a drop in the steady state membrane potential, but also concurrent with these phenomena increases the formation of superoxide, hydrogen peroxide, and Fenton\/Haber-Weiss generated hydroxyl radical. These oxidants increase the levels of cellular aldehyde\/ketones. Additionally, we find a five-fold increase in the levels of oxidant damaged mitochondrial DNA bases and increases in the levels of mtDNA nicks and blunt-ended breaks. Highly damaged mitochondria are characterized by having very low membrane potentials, increased superoxide\/hydrogen peroxide production, and extensively damaged mtDNA and proteins. These mitochondria appear to have undergone a permeability transition, an observation supported by the five-fold increase in Caspase-3 activity observed after Thimerosal treatment…We believe that this finding is important, particularly since the number of diseases in which mitochondrial dysfunction has been implicated are rapidly increasing.’ Martyn A. Sharpe, Andrew D. Livingston, and David S. Baskin, Department of Neurosurgery, The Methodist Hospital, Houston, Texas, USA – Journal of Toxicology, 06\/28\/2012<\/strong> http:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC3395253\/<\/a><\/strong><\/p>\n

Note: ‘at one hour of incubation (exposure to Thimerosal) we are not observing full blown apoptosis, which is characterized by nuclear DNA fragmentation, and are indeed observing the early phases of cell death…The damaged DNA is cytosolic (totality of the intracellular substance exclusive of mitochondria), not nuclear (membrane-bound organelle in eukaryotic cells), suggesting mitochondrial DNA (battery pack of your cells) damage.’<\/strong><\/div>\n
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\"\"<\/a>Meanwhile the CDC continues to trumpet the widespread use of Thimerosal in vaccines as safe, despite the growing mountain of scientific evidence to the contrary. ‘This strong study adds to the body of scientific evidence that thimerosal in vaccines is not harmful to children.’<\/a> CDC: Immunization Safety and Autism \u2013 Thimerosal and Autism Research chart <\/strong><\/div>\n
\u00a0<\/strong><\/div>\n
Thimerosal Mercury is added to vaccines austensibly to sterilize the giant multi-dose vats containing the serum. Even Vaccine & Pharmaceutical manufacturing giant Eli Lilly, who own the patent to Thimerosal for use as a preservative, have stated unequivocally, on their official Material Safety Data Sheet: ‘Exposure to mercury in utero and in children may cause mild to severe mental retardation and mild to severe motor coordination impairment<\/a>.\u2019<\/strong><\/div>\n
\u00a0<\/strong><\/div>\n
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What are the primary culprits which render an infant completely vulnerable to neuro-developmental disorders such as Autism?<\/strong><\/div>\n
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1. Chiefly a premature, multiple vaccine derived \u201cbreach\u201d of the delicate, underdeveloped \u201celectrical grid\u201d nerve center, designed to insulate the human Brain & Central Nervous System (Myelin sheath, Blood-Brain barrier, Meninges); coupled with\u2026<\/strong><\/p>\n

2. Severe dietary deficiencies (triggered by gluten, casein, iodized salts, sugars, trans fats), hastened by\u2026\u00a0<\/strong><\/p>\n

3. Pre-existing medical conditions and\/or compromised immunity (inherited vaccine derived mutagenic viral\/bacterial infections embedded in the DNA, passed on from mother to child via the placenta & colostrum) which leads to\u2026<\/strong><\/p>\n

4. Mitochondrial disfunction (battery pack of cells), decreased Methylation capacity (the loss of cell viability\/vitality), compounded by\u2026\u00a0<\/strong><\/p>\n

5. Glandular breakdown (The Thyroid produces T3 & T4 hormones\/Iodine Atoms. Iodine helps regulate metabolism in the body. A compromised immune system is much more vulnerable to infection & seasonal influenza. Vaccines undermine the immune system by introducing live viruses & toxic heavy metals to an already overloaded network. The synergy of immunological, neurological & physiological well being hangs in the balance. Thus the delicacy of our glands must be protected. Otherwise a domino effect of sickness & long term deterioration of health are inevitable. For children coping with Autism the impact of Thyroid deficiency is even that much greater), in addition to\u2026<\/strong><\/p>\n

Note: Every major organ & gland (comprising the Thyroid, Thymus, Pituitary, Pineal, Adrenal, Pancreas, Ovaries, Testis) are entirely interdependent, a magnificently delicate apparatus of interconnections, without any one of which, the entire system of operations will inevitably fail, leading to a chain-reaction of adverse metabolic breakdown, deterioration in effectiveness of your natural health & compromised immunity. The Thyroid Gland, in particular, serves a tremendous purpose in the body. It is key to overall health; considered a master gland which indirectly regulates your metabolism. The extent of its ability to function normally determines the viability of your heath \u2013 it is a bell weather indicator.<\/strong><\/p>\n

\u00a0\u00a0 6. An inability to sequester or chelate heavy metals from the body, particularly Thimerosal Mercury & Aluminum, due to an overwhelming early intervention of multiple toxic ingredients (primarily vaccine derived heavy metal-excipient-virus-<\/strong>bacterium type \u201csludge\u201d, Prescription drugs & antibiotics) which assault the baby\/young child at a critical stage in early development (as early as 12 hours old ie. Hepatitis B shot), exposing the child to\u2026\u00a0 <\/strong><\/p>\n

7. Subsequent underlying contamination of the \u201cbedrock\u201d gut (Yeast overgrowth, Gut Flora, Mycoplasma) which creates a perfect breeding ground for Leaky Gut Syndrome & ensuing Inflammatory Bowel Diseases (Celiac\/Crohn\u2019s Disease, Colitis); and further\u2026\u00a0<\/strong><\/p>\n

8. Ensuing depletion of vital nutrients (trace minerals & anti-oxidants) from the body. Common deficiencies amongst children with\u00a0 Autism frequently include: Vitamin A, B6\/B12, C, D3, E, Glutathione, Selenium. These are the body\u2019s primary antioxidants & trace minerals, essential to regulating Free Radicals (unpaired Electrons) throughout the body, staving off Cancer, Diabetes, Autism, Schizophrenia & the rapid macro-degeneration of cells.<\/strong><\/p>\n

Note: The Liver and Kidneys have important enzymes that change (synthesize) Vitamin D from the sun or food to the biologically active form of Vitamin D. In turn, the Lymphocytes (which service your lungs) also depend on Vitamin D3 (steroid hormone known as \u201ccholecalciferol\u201d derived primarily from direct exposure to sunlight & via fatty fish, egg yolks, and dairy products) in order to process Vitamins C & E, while regulating proinflammatory cytokines (those which make disease worse); thus staving off infections, ie. colds, influenza, asthma, bronchitis, pneumonia. In the case of children coping with\u00a0 Autism the mechanisms which normally enable the body to regulate all systems of functioning, to fight incoming infections, or process nutrients effectively, are severely compromised prematurely, which results in the rapid depletion of vital antioxidants & trace minerals, meant to service a child throughout the critical, early stages of development. VRM<\/strong><\/p>\n

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

\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014\u2014<\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/span><\/strong><\/strong><\/p>\n

Breaking News: Childhood Influenza-Type Pneumonia Directly Linked to PCV Vaccine Bacterial Cross-infection \u00a0<\/span><\/strong><\/strong><\/p>\n

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Children who succumb to seasonal Flu, either via death or serious long-term illness (in particular those tracked since 2009), are subsequently found to have been 8 times more predisposed to a Methicillin-resistant Staphylococcus Aureus (MRSA) bacterial co-infection occurring in the lungs. It is also significant that routine prescription anti-bacterials\/virals (chiefly Vancomycin Hydrochloride Capsules & Oseltamivir\/Tamiflu), widely distributed globally to ostensibly combat flu-like symptoms, have in fact been the tipping point which has worsened such conditions, hastening Kidney failure, Myocarditis (inflammation of the Heart Muscle) & numerous instances of sudden death. <\/strong><\/p>\n

Note: ‘8 times more predisposed to a Methicillin-resistant Staphylococcus Aureus (MRSA) bacterial co-infection occurring in the lungs.’ <\/strong><\/p>\n

All vaccinated children in the Western hemisphere are now carriers of what is known as MRSA (Methicillin-resistant Staphylococcus aureus\/anti-biotic resistant super-bug), due to cross-infection primarily from the routine administering of the Pneumococcal (PCV) Vaccine \u2013 in combination with post vaccination anti-biotic & anti-viral drug treatment, an accumulative assault which strips a child of his\/her natural anti-biotic resistance whilst infecting them with a host of bacterial serotypes (1, 3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F, 23F) \u2013 <\/strong><\/p>\n

\u2026leaving them totally vulnerable to Middle ear infections, high-grade seizures, Pneumonia, Myocarditis (inflammation of the heart muscle), Endocarditis (inflammation of the inner lining of the heart valves), Osteomyelitis (acute or chronic inflammatory process of the bone), Toxic Shock Syndrome (TSS), Bacteremia (presence of viable bacteria in the circulating blood) & Septicemia (blood poisoning), Meningitis (inflammation of the membranes\/meninges surrounding the brain & spinal cord, usually due to the spread of an infection), and even sudden death. The current generation have literally become unwitting hosts to a form of bacterial roulette, an ideal breeding ground for the proliferation & weaponizing of bacterial infections. VRM<\/strong><\/p>\n

\u2018Since\u00a0 2000, several reports have documented the presence of MRSA infections\u00a0 in previously unaffected outpatient populations\u2026a dramatic shift in\u00a0 the microbial flora of soft tissue infections has occurred recently in\u00a0 the United States. Popovich et al. in 2008 reported data from 2000-2006\u00a0 in Chicago\u2019s Stroger Hospital\/Rush University Medical Center that showed\u00a0 a stable rate of hospital acquired strains of MRSA infections, but a\u00a0 rapidly increasing rate of community acquired strains of MRSA seen in\u00a0 the hospital from 24% between January 2000 and June 2003 to 49% between\u00a0 July 2003 and December 2006.<\/a>‘\u00a0<\/strong>Prevalence of Methicillin Resistant Staphylococcus Aureus in Upper Extremity oft Tissue Infections at Jackson Memorial Hospital, Miami-Dade County, Florida, 2009<\/strong><\/div>\n
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Note: This increase coincides precisely with the release of the first Pneumococcal (PCV)\u00a0 Vaccine on the market \u2013 \u2018PCV7,\u00a0 containing the 7 most common pneumococcal serotypes causing invasive\u00a0 infections in children in North America was licensed in the US and\u00a0 recommended for routine use in infants in 2000<\/a>.\u2019<\/strong><\/div>\n
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\u2018A recent study by the Centers for Disease Control and\u00a0 Prevention (CDC) found that of the 36 children who died from H1N1 from\u00a0 April to August (2009), six had no chronic health conditions. But all of them\u00a0 had a co-occurring bacterial infection. The most common co-occurring\u00a0 infection that causes flu-related deaths is staphylococcus aureus<\/a>. A\u00a0 third of the population carries it, most in their nose or on their skin.\u00a0 The flu causes upper respiratory damage, which allows the staph to make\u00a0 its way into the lungs.\u2019 ‘Co-detection of Pandemic (H1N1) 2009 Virus and Other Respiratory Pathogens’, CDC<\/strong><\/div>\n<\/div>\n

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Note: \u2018The most common viral pathogens in the pandemic (H1N1) 2009\u2013negative\u00a0 samples were from the family Picornaviridae: coxsackie\/echovirus (due to cross-contamination from the Inactivated Polio Vaccine\/IPV), and rhinovirus (due to cross-contamination from the Hepatitis B Vaccine & H1N1\/Seasonal strain type Influenzae Vaccine)\u2026The most commonly co-detected pathogens were S. aureus (due to cross-contamination from the Pneumococcal Vaccine\/PCV), S. pneumoniae (due to cross-contamination from the Pneumococcal Vaccine\/PCV & the H1N1\/Seasonal strain type Influenzae Vaccine), and H. influenzae (due to cross-contamination from the Haemophilus influenzae type B Vaccine\/HIB).<\/a>\u2019\u00a0 Centres For Disease Control: Co-detection of Pandemic (H1N1) 2009 Virus and Other Respiratory Pathogens, December 2010<\/strong><\/p>\n

Clearly society has reached its saturation point with the widespread over-use\u00a0of anti-biotics; which has given rise to the emergence of\u00a0 \u2018multidrugresistant staphylococci\u2019, potentially the greatest of threats\u00a0 to our natural immunity, in terms of its resilience in the environment\u00a0& virulence in the human host. \u2018Spontaneous chromosomal mutations have also played a role in the emergence of clinically important resistance<\/a>\u2018\u2026\u2019It\u2019s possible methicillin- resistant Staphylococcus aureiis will become untreatable.<\/a>\u2018<\/strong><\/p>\n

The Vaccine Resistance Movement has recently uncovered scientific proof implicating the PCV vaccine with Staphylococcus aureus and Streptococcus pneumoniae infection in babies\/young children having received the shot:\u00a0<\/strong><\/p>\n

Role of Staphylococcus aureus Catalase in Niche Competition against Streptococcus pneumoniae: \u2018Nasal\u00a0colonization by Staphylococcus aureus is a major predisposing factor\u00a0for subsequent infection. Recent reports of increased S. aureus\u00a0colonization among children receiving pneumococcal vaccine implicate\u00a0Streptococcus pneumoniae as an important competitor for the same niche.\u00a0Since S. pneumoniae uses H2O2 to kill competing bacteria, we\u00a0hypothesized that oxidant defense could play a significant role in\u00a0 promoting S. aureus colonization of the nasal mucosa. Using targeted\u00a0mutagenesis, we showed that S. aureus expression of catalase contributes\u00a0significantly to the survival of this pathogen in the presence of S. pneumoniae both in vitro and in a murine model of nasal cocolonization.<\/a><\/strong><\/p>\n

Multiple\u00a0studies have shown that colonization of the upper airway with S.\u00a0pneumoniae is negatively correlated with S. aureus colonization, and\u00a0 introduction of the S. pneumoniae vaccine has increased the rate of S.\u00a0aureus nasal colonization. By eradicating carriage of S. pneumoniae\u00a0vaccine strains, immunization removes an important niche competitor that\u00a0 utilizes H2O2 to restrict colonization by other bacteria. In this\u00a0study, we showed that the S. aureus catalase is a major factor in S.\u00a0aureus defense against S. pneumoniae killing due to neutralization of secreted H2O2. H2O2 is used as an antimicrobial factor by many other\u00a0microbes, including Streptococcus sanguinis in the oral cavity and\u00a0 lactobacilli in the vagina, two sites frequently cocolonized by S.\u00a0aureus. Thus, it could be speculated that in S. aureus catalase is an\u00a0important tool for securing a niche on multiple mucosal surfaces in the\u00a0human host. The presence of catalase may also explain the preferential\u00a0 survival of WT S. aureus compared to the \u0394KatA mutant in the cotton rat\u00a0 model of nasal colonization previously reported by Cosgrove and\u00a0coworkers. S.\u00a0aureus encodes a number antioxidants, including, alkyl hydroperoxide\u00a0reductase, and staphyloxanthin, which may supplement catalase in defense\u00a0against H2O2-producing organisms, such as S. pneumoniae.<\/a>‘ Bonggoo Park, Victor Nizet, and George Y. Liu, Journal of Bacteriology, January 2008<\/strong><\/p>\n

Note: \u2018Recent reports of increased S. aureus colonization\u00a0 among children receiving pneumococcal vaccine implicate Streptococcus\u00a0pneumoniae as an important competitor for the same niche.\u2019<\/strong><\/p>\n

\u2018Bacteria that cause childhood pneumonia and meningitis have\u00a0 evolved to evade vaccines by swapping bits of their genome with other\u00a0 bacteria, according to a new study. Vaccines that protect against these\u00a0so-called pneumoccoccal infections are designed to recognise a material\u00a0 on the outer surface of a bacterium\u2019s cell called polysaccharide. Each\u00a0of more than 90 kinds, or \u201cserotypes\u201d, of these bacteria have a different polysaccharide coating.<\/strong><\/p>\n

In 2000, a vaccine that targeted seven serotypes proved\u00a0 highly effective when introduced in the United States. The same formula \u2013\u00a0 which also prevented transmission from children to adults \u2013 was adopted\u00a0 in Britain. Over time, however, the vaccine worked less well, so\u00a0researchers led by Rory Bowden at the University of Oxford set out to\u00a0discover why. Combining cutting-edge genetic analysis with epidemiology, which examines how disease spreads, they found that the deadly\u00a0pathogens escaped detection by swapping genes with other, slightly\u00a0 different, bacteria. Remarkably, the exchanged genetic material came\u00a0 from precisely that part of the genome responsible for making the cell\u2019s\u00a0 coating \u2013 the area targeted by the vaccine. The bacteria, in other\u00a0words, had kept their virulence intact but changed their outward\u00a0 appearance.<\/strong><\/p>\n

The researchers identified several such \u201crecombined\u201d\u00a0 serotypes resistant to the vaccine, and one in particular that had\u00a0 spread across the US from east to west over several years. They also\u00a0 observed \u2013 for the first time outside a laboratory \u2013 that the bugs could\u00a0 swap several parts of their respective genomes at once. \u201cThis\u00a0 is of particular concern, as recombination involving\u00a0 multiple fragments of DNA allows rapid and simultaneous exchange of key\u00a0 regions of the genome within the bug, potentially allowing it to quickly\u00a0 develop antibiotic resistance,\u201d the researchers said. In both the US\u00a0 and Britain, the original vaccine has been replaced with a new one that\u00a0 targets 13 rather than seven of the telltale serotypes. But the\u00a0 scientists caution that the bacteria will continue to morph into new\u00a0 forms.<\/a>\u2019<\/strong><\/p>\n

Note: \u2018\u2026the bacteria will continue to\u00a0morph into new forms\u2019.<\/strong><\/p>\n

This reformulating or \u201cmorphing\u201d nature of the Staphylococcus\u00a0\u00a0 aureus-type pathogen is indicative of years spent being sliced and\u00a0 re-spliced in top Level Bio-laboratories; while overcoming the body\u2019s\u00a0 natural\u00a0 anti-biotic defenses through prolonged incubation in the host species \u2013\u00a0 increasingly compromised generation to generation by the over-use of\u00a0 Prescription anti-biotics and vaccine derived heavy\u00a0 metal\/excipient\/virus & bacterium \u201csludge\u201d toxicity.<\/strong><\/div>\n
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The\u00a0 routine administering of post Influenza vaccination Prescription Drugs\u00a0 (Vancomycin & Oseltamivir aka Tamiflu) led to serious adverse\u00a0 interactions which not only hastened the critical conditions of those\u00a0 who sought hospital care, but may, in fact, have triggered the premature\u00a0deaths of most, if not all children who succumbed to 2009\u2019s laboratory\u00a0produced \u201cnovel\u201d strain of H1N1 (2 parts Swine Flu, 1 part Human Flu, 1\u00a0part Avian Flu).<\/strong><\/div>\n
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\u2018The detection of an increased number of A(H1N1) viruses with resistance to oseltamivir (Tamiflu<\/a>)\u00a0\u00a0 was initially reported to WHO by Norway on 25 January 2008. The\u00a0 viruses\u00a0 carried a specific neuraminidase (NA) mutation (H274Y) that\u00a0 confers\u00a0 high-level resistance to oseltamivir in N1-containing influenza\u00a0viruses. Prior to the recent report from Norway, such resistance was\u00a0 rarely\u00a0 observed in community isolates of influenza A or B. During the\u00a0 previous\u00a0 northern hemisphere winter season (2006\/2007), surveillance\u00a0through the\u00a0Global Influenza Surveillance Network (GISN) laboratories found no\u00a0oseltamivir-resistant H1N1 viruses among isolates from Japan\u00a0or Europe, and less than 1% prevalence among H1N1 isolates from the\u00a0United States\u00a0of America.<\/strong><\/p>\n

The mutation in N1 neuraminidase of human influenza virus which confers high-level resistant to oseltamivir<\/a> is a single amino acid substitution of the relevant histidine (H) to tyrosine (Y) at position 275. Most of the early work on structure and inhibitor design is based on two other subtypes (N2 and N9) and the\u00a0corresponding amino acid in these subtypes is at position 274.\u00a0Consequently, some scientists use \u2018N2 numbering\u2019 (H274Y) and some use the actual \u2018N1 numbering\u2019 (H275Y).\u2019 WHO http:\/\/www.who.int\/influenza\/patient_care\/antivirals\/oseltamivir_summary\/en\/<\/a><\/strong><\/p>\n<\/div>\n

The truth is the body is being systematically targeted\u00a0 & broken down from all sides, creating a perfect storm of toxicity\u00a0 which has derailed the inherent functionality of our natural immunity\u00a0 generation to generation; thereby opening the door to widespread ill\u00a0 health. Western medicine, however they spin its so called \u201cprogress\u201d,\u00a0 continually offers the antithesis of a natural solution.<\/strong><\/p>\n

It is no longer a coincidence to suggest a correlation\u00a0between \u201cnatural vs. manufactured (prescription)\u201d anti-biotic\/anti-viral breakdown in the body and\u00a0 \u201cnatural vs manufactured (prescription)\u201d anti-biotic\/anti-viral resistance overload proliferating in the environment. Approximately \u20182 out of every 100 people carry a strain of staph that is resistant to these antibiotics<\/a>\u2018.\u00a0\u00a0 We have reached the saturation point as a species; with the continued\u00a0\u00a0 oversight of Western Allopathic Medicine, focusing solely on treating\u00a0(and thereby exacerbating) symptoms rather than seeking out &\u00a0remedying (embracing) the underlying cause.<\/strong><\/p>\n

\u2018Children with preexisting neurologic conditions and immune\u00a0compromise were at increased risk of pH1N1-associated death after PICU\u00a0admission. Secondary complications of pH1N1, including myocarditis\u00a0(inflammation of the heart muscle), encephalitis (inflammation of the brain & meninges),\u00a0and clinical diagnosis of early presumed MRSA (Methicillin-resistant\u00a0\u00a0 Staphylococcus Aureus) coinfection of the lung, were mortality risk\u00a0\u00a0 factors.\u2019 Published in American Academy of Pediatrics, 09\/31\/11 http:\/\/pediatrics.aappublications.org\/content\/early\/2011\/11\/04\/peds.2011-0774.abstract?sid=2f7367a0-a5d8-4ae8-b2f1-b9e16e543085<\/a><\/strong><\/p>\n

\u201cThere\u2019s\u00a0more risk for MRSA (methicillin-resistant Staphylococcus aureus) to\u00a0become invasive in the presence of flu or other viruses. These deaths in\u00a0co-infected children are a warning sign. This is especially alarming\u00a0given the rising rates of MRSA infections being carried widely among children. It is not common in the U.S. to lose a previously healthy\u00a0child to pneumonia. Unfortunately, these children had necrotizing\u00a0pneumonia eating away at their tissue and killing off whole areas of the\u00a0lung. They looked like immunocompromised patients in the way MRSA went through their body. It\u2019s not that flu alone can\u2019t kill \u2013 it can \u2013 but\u00a0 in\u00a0most cases children with flu alone survived\u2026The more antibiotics we\u00a0\u00a0 take, the more we colonize ourselves with antibiotic-resistant\u00a0organisms\u00a0such as MRSA<\/a>.\u201d Adrienne G. Randolph, MD, Division of Critical Care Medicine at Children\u2019s Hospital Boston<\/strong><\/p>\n

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\u2018During the 2009 H1N1 influenza pandemic, many previously\u00a0healthy children became critically ill, developing severe pneumonia and\u00a0respiratory failure, sometimes fatal. The largest nationwide investigation to date of influenza in critically ill children, led by\u00a0Children\u2019s Hospital Boston, found one key risk factor: Simultaneous infection with methicillin-resistant Staphylococcus aureus (MRSA) increased the risk for flu-related mortality 8-fold among previously\u00a0healthy children. Moreover, almost all of these co-infected children\u00a0were rapidly treated with vancomycin, considered to be appropriate\u00a0treatment for MRSA. The fact that they died despite this treatment is\u00a0especially alarming given the rising rates of MRSA carriage among\u00a0children in the community.<\/strong><\/p>\n

While most of the children critically ill with H1N1 had one\u00a0or more chronic health conditions that increased their risk, such as asthma, neurologic disorders or compromised immune systems, 251 children\u00a0(30 percent) were previously healthy. Among these otherwise healthy\u00a0children, the only risk factor that was identified for death from influenza was a presumed diagnosis of MRSA co-infection in the lung \u2013 which increased the risk for mortality 8-fold (P<0.0001). 88 percent\u00a0of the children admitted to the ICU received Tamiflu (oseltamivir)\u00a0\u00a0\u00a0 during their stay, but only 6 percent had received it prior to hospital\u00a0admission\u2026The study also found that most of the MRSA co-infected children who died had received vancomycin promptly at or before ICU\u00a0admission.\u2019 Children\u2019s Hospital, Boston http:\/\/www.childrenshospital.org\/newsroom\/Site1339\/mainpageS1339P791.html<\/a><\/strong><\/p>\n

Note: \u201888 percent of the children admitted to the ICU received Tamiflu (oseltamivir) during their stay…’<\/strong><\/p>\n

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

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

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VRM Editorial:<\/strong><\/strong> The Trans-humanist war against humanity <\/span><\/strong><\/p>\n

\"\"<\/a>Nanotechnology represents the cornerstone of 21st Century advanced scientific research, but once again indicates a hubris & fundamental disregard for nature; and a gross miscalculation of nature\u2019s retaliatory instinct. Natural immunity will have no place in this so called \u201cbrave new world\u201d. The Trans-humanist Elites financing this dark revolution believe they will one day merge with the machine, in the wake of humanity\u2019s orchestrated demise\u2026a fate they have crafted for generations from behind closed doors, with nothing but malace in their withered hearts. Love & life will ultimately endure, and our hopes for a bright future will never be blown asunder by these misguided control freaks\u2026and in the end Nature will once again prevail. VRM <\/strong><\/div>\n
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\u2018One concern about nanotechnology\u2019s unintended consequences raises the question of the uncontrolled development of self-replicating nanoscale machines. A number of very serious technical challenges would have to be overcome before it would be possible to create nanoscale machines that could reproduce themselves in the natural environment. Some of these challenges appear to be insurmountable with respect to chemistry and physical principles, and it may be technically impossible to create self-reproducing mechanical nanoscale robots of the sort that some visionaries have imagined.<\/a>\u2019 National Science Foundation: Societal Implications of Nanoscience and Nanotechnology<\/strong><\/p>\n

See VRM: The Rockefeller Foundation Drafts A Post-Pandemic Scenario<\/a> <\/strong><\/p>\n

See VRM: Birth of Medical & Scientific Dictatorship \u2013 Future Scenarios<\/a> <\/strong><\/p>\n

See VRM: Pandemic Preparedness & The Dark Agenda Ahead<\/a> <\/strong><\/p>\n

See VRM: Morgellons Syndrome & Chemtrails<\/a> <\/strong><\/p>\n<\/div>\n

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VRM Editorial: Architecture of The<\/strong> Human Body\u00a0 <\/strong><\/span><\/strong><\/p>\n

\"\"<\/a>The human body is conceived much like the structure of a modern house. The foundation ideally consists of a solid framework of evenly distributed beams & supports built upon a reinforced bedrock – analogous to a healthy newborn baby. <\/strong><\/p>\n

The basement area of the house headquarters the central plumbing unit, including the primary \u201celectrical grid\u201d nerve center, a delicate, bio-conductive (bio-electric) circuit board that runs throughout the entire house, which enables all vital systems there-in to function & co-ordinate, maintains power, lighting, temperature balance; servicing all the rooms & corridors throughout the upper floors via an elaborate piping & drainage system interlacing the overall design – analogous to the 3 primary core \u201celectrical grid\u201d stations encasing the nerve center\/brain of the human body (comprising the Blood-Brain barrier, Myelin sheath & Meninges). <\/strong><\/p>\n

You also have a complex array of wires & cables coursing throughout the house, central exchanges, fuses, outlets & layers of inter-connections – analogous to the 60,000 miles of blood vessels coursing throughout your body, a vast array of highways & byways & tributaries that are all inter-connected. <\/strong><\/p>\n

The interconnection (fluidity) of the \u201celectrical grid\u201d nerve center” and the corresponding wires & cables coursing throughout the house is analogous to the highly sensitive electro-chemical network (apparatus) of neurons & ions coursing throughout your brain, enabling messages to circulate from your brain cells throughout the body & back; the regulating of organs, your bloodstream, Heart, Kidney, Liver function (chelating & sequestering), the operation of one\u2019s senses & warning signs – everything related to overall system co-ordination & metabolisim is managed via this delicate bio-conductive process.<\/strong><\/p>\n

Picture a bowl of water filled to the brim, situated just above the main circuit board. This is analogous to a baby’s brain during the critical stages of early development. A newborn baby has no Blood-Brain barrier (physiological mechanism that alters the permeability of brain capillaries so that some substances, such as certain drugs, are prevented from entering brain tissue, while other substances are allowed to enter freely) on the brain \u2013 so that vital, unfinished area is still completely raw & vulnerable. The Blood-Brain barrier takes no less than 7 months to establish its primary protective shielding. Any type of immune-stimulation or disruption, such as Vaccine-derived excitotoxicity (destruction of entire synapses & connector neurons in the brain from excess Glutamate transmition), causes the water to spill over its edges, thereby damaging the overall functionality of the primary circuit board. <\/strong><\/p>\n

The synergy of vaccine derived heavy metal-virus-mycoplasma-excipient toxicity \u201csludge\u201d targets the 3 primary core \u201celectrical grid\u201d stations encasing the nerve center\/brain \u2013 kin to throwing water over a main keyboard operating system. In the event the Blood-Brain barrier, Myelin sheath & Meninges are breached, particularly at such a premature\u00a0stage in early childhood development, neuro-developmental disorders such as Autism will inevitably follow in many instances. <\/strong><\/p>\n

The rooms which encompass the house are fully dependent on the guts of the operation to co-ordinate each aspect simultaneously & thus ensure a healthy environment in which to function. Children with Autism Spectrum Disorder have had the rug pulled out from under them at a critical stage of early development, depleted of their vital mineral & antioxidant base, stripped of Mitochondrial & Thyroid efficiency\/functionality, their delicate \u201celectrical grid\u201d nerve center violated prematurely \u2013 all of which significantly inhibits the capacity of the body to carry out its normal systems of operation. The gut level \u201cplumbing\u201d crisis, a hallmark of Autism, is the end result of a \u201chouse\u201d in crisis; ground zero for neurological & neuro-developmental disfunction.<\/strong><\/p>\n

Detoxification & restoration of the body can only be accomplished by focusing on the overall design. Depending on the extent of vaccine injury effecting your specific constitution, it can be measured, in terms of degrees, somewhere on the scale leading to Autism. Those of us fortunate enough to have avoided reaching this extreme must take stock & learn from these individuals. The often debilitating conditions they endure on a daily basis MUST serve as a bell-weather warning, a road-map to navigating our way out of the cavernous lair of ill-health. After all, many children in these tough circumstances are succeeding in reversing the symptoms of Autism & repairing their window to natural health through the intervention of a strict dietary protocol. VRM<\/strong><\/p>\n

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VRM Editorial<\/strong>: <\/span>Hospital Birthing vs. Home Birthing<\/span> <\/strong><\/p>\n

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My chief concern with choosing a hospital birth – even if you fill out the proper vaccine waiver forms that your hospital provides you (and they’ll give one to you reluctantly after attempting to dissuade you), you still might have to contend with mistakes made by the local nursing staff on hand that day. During that chaotic period of several hours, when you’re both exhausted (especially the mother obviously), in which they wisk your baby away for a health check, weighing, acquiring an official blood sample (which you might consider refusing, given the fact that it’s sent to a Federal blood data bank as an identity marker), all the standard post-delivery procedures, the nurses MAY inadvertently overlook the fact that you signed that waiver, and give your baby the dangerous Hepatitis B shot regardless (including the excessive and unnecessary Vitamin K shot by the way, given during the post-delivery phase<\/a>). At that point the die is cast and there’s unfortunately no reversing the decision made. But a home birth ensures you true peace of mind, that you have the full autonomy to make all these critical decisions in the heat of the moment (as is proper), and therefore guarantee that any such procedural mistakes, as often occur on busy hospital wards, will be avoided. <\/strong><\/strong><\/div>\n
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‘Having worked in hospitals for over twenty years as RN, I can validate the “oversight” re. vaccine protocol.’\u00a0Viewpoint\u00a0of a veteran Registered Nurse <\/strong><\/div>\n
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This is an important step in ultimately reclaiming self-determination of the body, and you shouldn’t feel the slightest bit insecure about this type of pivotal decision. Just be sure to plan well ahead and have all the appropriate support (personel & equipment) on hand to ensure your home birth is a glorious experience for the baby & you. Talk to other mothers who’ve been through it. They’ll echo the same sentiment in most if not all cases. It’s a natural, toxin-free, comparatively STRESS FREE introduction into the world for your baby AND a life-changing experience for you. It’ll also bring your entire family closer together, a celebration to be cherished for years to come. <\/strong><\/div>\n<\/div>\n
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\"\"<\/a>T<\/strong>he Hepatitis B Vaccine is administered to newborn babies within the first 12 hours after birth (3 eventual doses). Not only is the shot completely unneccesary, but it is also directly linked to resulting Mitochondrial disfunction (a hallmark symptom of Autism); including premature apoptosis or \u201cprogrammed\u201d type cell death. The Hepatitis B vaccine factors into the eventuality of Early Onset Autism, since it represents the earliest premature breach of a baby\u2019s delicate, under-developed \u201celectrical grid system\u201d (Myelin sheath, Meninges & Blood Brain Barrier). <\/strong><\/div>\n
\nNote: \u2018Exposure of Hepa1-6 cells to a low dose of adjuvanted hepatitis B vaccine leads to loss of mitochondrial integrity, apoptosis induction, and cell death\u2026In vivo apoptotic effect of hepatitis B vaccine was observed in mouse liver.\u2018<\/a> <\/strong><\/div>\n
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\u00a0<\/strong>Official Package Insert: \u201810 \u00b5g\/mL\u00a0 Each 1 mL dose of sterile suspension contains hepatitis B surface antigen 10 \u00b5g adsorbed onto approximately 0.5 mg of amorphous aluminum hydroxyphosphate. Formaldehyde-treated. Thimerosal (mercury derivative) 1:20,000 (50 \u00b5g\/mL) has been added only to the preservative-containing formulations. 3-dose vials of 3 mL<\/a><\/strong>\u2018\u2026\u2019<\/strong>A portion of the hepatitis B virus gene, coding for HBsAg, is cloned (synthetic genomics) into yeast, and the vaccine for hepatitis B is produced from cultures of this recombinant yeast strain.<\/a>\u2018<\/strong><\/p>\n

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

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Senior World Bank Globalist admits to Vaccination Campaign “targeted action”-type “Policy Levers” for ongoing Global Population Management (Bioethics aka Eugenics) Strategy<\/span><\/strong><\/div>\n
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‘A population policy is a set of interventions implemented by government officials to better manage demographic variables and to try to attune population changes (number, structure by age and breakdown) to the country\u2019s development aspirations. Population policies attempt to modify the various components of population growth. This may concern mortality or fertility, when it is felt to be too high or too low. This may also involve regulating international migratory flows or fostering internal migration currents, as was the case in Indonesia with the transmigration policy (population relocations on the archipelago). Finally, we may think of policies to support urbanization and to try to manage slums. More recently, the developed countries have also focused on their aging population problem. The means used to implement population policies are \u201cpolicy levers\u201d or targeted actions such as vaccination campaigns or family planning to change certain key variables.’ John May PhD. Lead Population Researcher for Africa & Senior Population Specialist, Africa Region, World Bank<\/strong><\/div>\n
\"\"<\/a>Interview with John F. May concerning the demographic future of the planet (Sens Public), Center for Global Development, October 2, 2012 http:\/\/www.cgdev.org\/content\/article\/detail\/1426540\/<\/a>rticle\/detail\/1426540\/<\/a><\/strong><\/div>\n
John May http:\/\/www.zoominfo.com\/people\/May_John_161088918.aspx<\/a><\/strong><\/div>\n
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See VRM: The Problem With Vaccines Part 3 \u2013 Synthetic Genomics & The Death Of Natural Immunity<\/strong><\/div>\n
http:\/\/vaccineresistancemovement.org\/?p=6880<\/a><\/strong><\/div>\n
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Recommended treatment for puncture wounds, cuts &\u00a0lesions:<\/span> <\/strong><\/p>\n

1. Apply Tea Tree Oil drops to exposed\/infected area. <\/strong><\/p>\n

2. Apply Oil of Oregano drops to exposed\/infected area. <\/strong><\/p>\n

3. Next, apply a generous mixture (balm) of Bee Propolis & Comfrey extract to exposed\/infected (including burn related) area.\u00a0\u00a0<\/strong><\/p>\n

4. Wrap in a non-toxic type gauze (for appropriate period – typically 2-3 days) to allow for natural, gradual healing process.\u00a0<\/strong><\/p>\n

5. Remove gauze and apply Organic Coconut Oil (virgin) to the entire area of the abrasion (puncture wound, cut\/lesion), until the newly formed skin is fully healed.<\/strong><\/p>\n

Repeat steps 1-4 if necessary, depending on the extent of the injury incurred.\u00a0<\/strong><\/p>\n

Note: Avoid getting a Tetanus shot, even though your doctor, hospital or clinic staff will vehemently recommend it, and inevitably ridicule or intimidate you into complying with the standard protocol. The vast majority of mainstream doctors\u00a0are indoctrinated with short-sighted Medical thinking and most often know nothing about the benefits of natural immunity.<\/strong><\/p>\n

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VRM Editorial: On The Road To Natural Immunity<\/span><\/strong><\/p>\n<\/div>\n<\/div>\n

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Research conducted by the Vaccine Resistance Movement is routinely ignored by Mainstream Corporate & Medical Mafia financed Media outlets. There’s a significant reason for that. This revelatory information could unseat & derail the entire Western Medical Establishment machine, thereby threatening the iron grip they have on our communities around the world; a multi-billion dollar empire fueled by dependency on Government lies & Western Allopathic Medical “know-how” in determining our overall health.<\/strong><\/p>\n

It’s up to you now to get the word out, and to begin that journey back onto the road toward natural immunity & ultimately…reclaiming your inherent right to self-determination of the body.<\/strong><\/p>\n

There is simply no middle ground, no compromise position in determining the merits of Vaccine safety & efficacy, the whole basis for & methodology behind Immunization as a means of overcoming viral & bacterial type infections and theoretically safeguarding the body\u2019s immunological capacity. Either you are FOR Immunization or firmly AGAINST it. Those parents who subscribe to the belief that they are somehow erring on the side of cautionary wisdom by allowing their child\/children to be vaccinated gradually or partially, according to the current Standard Immunization Schedule established by the CDC & local Government appointed Health \u201cexperts\u201d, are woefully mistaken. The ENTIRE Vaccine Industry is a fraud, period. All vaccines, by their very nature, play off each other \u2013 a \u201csynergistic\u201d chain-reaction; triggering further infections & disorders. In many cases the very signature disease\/disorder they claim to protect you against is PRECISELY that which they inadvertently spread. \u00a0 <\/strong><\/p>\n

Natural Immunity is designed to take on and withstand any incoming infections which threaten your survival. The body can only do this when it is naturally, gradually exposed to disease & infectious agents lurking in the environment. We have been societally engineered by a blind-sighted Technocracy, deceived into believing all the lies put forth by Western Allopathic Medicine, the whole mistaken ideology & foundation surrounding Immunization as a practice; an antithetical approach which runs counter to nature, that of COMBATING or shielding yourself off from the environment by injecting toxins into deep muscle tissue\/subcutaneously, artificially shocking or jump-starting the body into recognizing external \u201cthreats\u201d, rather than holistically EMBRACING all that we come in contact with, thereby re-enforcing, through HARMONY, the inherent properties of natural immunity. We\u2019re not meant to be hermetically sealed organisms, but that is ultimately where the Medical Establishment intends you to be. And if you take their instructions to heart, then your body will inevitably become a breeding ground for long-term infections, degeneration & disease, neurological disruption \u2026and ultimately, a perfect environment for otherwise AVOIDABLE hybrid forms of cancer.<\/strong><\/p>\n

Do you really want this to be your fate? Do you really think you have exhausted your capacity to make a difference, to put a stop to these ongoing crimes against humanity? Have you really made an effort to discard your manufactured reality, that which the systems of power have forced into your consciousness through generations of social engineering, a controlled mainstream media & education system funnel of lies, distractions and cover-ups designed to isolate you from the truth, that true freedom is within our reach? Do you care at all about preserving what\u2019s left of your natural immunity, your capacity to embrace self-determination of the body? Do you even know what it is any more? Are we really a community of sheeple, with our minds & our eyes & our hearts closed to Globalist imposed tyranny, resigned to this unfathomable fate, having turned against all the principles of independence which our ancestors fought so hard to nurture & protect, unable or unwilling to take charge of the wheel?<\/strong><\/p>\n

When will it end? When will we begin to recognize that we have all been lied to by our governments about virtually everything that matters? Perhaps when it is too late, when we will have no choice but to capitulate to these control freaks, as we walk solemnely into that bleak future scenario with our spirits broken? Our ancestors are waiting & watching for us to rise up and RECLAIM that which is inherent to life, a genuine freedom which they once coveted by hook or crook, in far more desperate circumstances. It is up to you, as it has always been. VRM<\/strong><\/p>\n

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\u00a0 <\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/strong><\/p>\n","protected":false},"excerpt":{"rendered":"

Breaking News:\u00a0The vanguard of\u00a0current Influenza Vaccine formulations are utilizing cloned (chemically synthesized & replicated in a laboratory) insect-virus vectors in which to harness the Influenza viruses for mass production. No matter which route you take in terms of the application of 21st century vaccine production technology (cloning), all roads will inevitably lead to otherwise avoidable […]<\/p>\n","protected":false},"author":2,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"open","ping_status":"open","template":"","meta":{"footnotes":""},"class_list":["post-10934","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=\/wp\/v2\/pages\/10934","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=\/wp\/v2\/types\/page"}],"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=10934"}],"version-history":[{"count":120,"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=\/wp\/v2\/pages\/10934\/revisions"}],"predecessor-version":[{"id":13604,"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=\/wp\/v2\/pages\/10934\/revisions\/13604"}],"wp:attachment":[{"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=10934"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}