Breaking News: The vanguard of current 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

It should come as no surprise that the flagship model, the first major Cloned cell-based vaccine ever for mass production, FLUVIRIN®, manufactured by Novartis Vaccines, was introduced in the Fall of 2011 in the United States with the annual Flu shot; touted as a ‘Recombinant Trivalent Hemagglutinin Protein-based Influenza Vaccine‘. ‘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).’

Note: Package Insert – ‘FLUVIRIN® 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.’

Novartis Vaccines & Diagnostics has been awarded a $487 million contract by the US Dep’t 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, to produce ‘50 million doses of seasonal trivalent flu vaccine, and up to 150m doses of monovalent vaccine‘ in preparation for a potential Pandemic.

‘If a flu pandemic strikes the United States, a Novartis  (NYSE: NVS )  plant in North Carolina now stands ready to respond with vaccine techniques that offer speed and scalability advantages over traditional 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 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

Barda is leveraging its options in this highly lucrative “marketplace“, by simultaneously finacing the competition. One such manufacturer entering the arena, Protein Sciences Corporation (PSC), with the help of a $147 million joint contribution (‘awarded a contract in June 2009 to support further development and scale-up of our flu vaccines, FluBlok and PanBlok’), have launched a major campain to unseat Novartis, with their very own misguided cloning-type patent for vaccine production, involing the replication of “transgenic insect cells” for use in vaccine production. ‘We have established a broad patent estate on influenza vaccines produced using recombinant technology in our expresSF+ cells.

ExpresSF+ Cells Patent ‘Baculovirus-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).’


Breaking News: Study Links Thimerosal Use in Vaccines with Premature Cell Death & Mitochondrial Disfunction 

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

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.’
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.’ CDC: Immunization Safety and Autism – Thimerosal and Autism Research chart
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.’
What are the primary culprits which render an infant completely vulnerable to neuro-developmental disorders such as Autism?

1. Chiefly a premature, multiple vaccine derived “breach” of the delicate, underdeveloped “electrical grid” nerve center, designed to insulate the human Brain & Central Nervous System (Myelin sheath, Blood-Brain barrier, Meninges); coupled with…

2. Severe dietary deficiencies (triggered by gluten, casein, iodized salts, sugars, trans fats), hastened by… 

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…

4. Mitochondrial disfunction (battery pack of cells), decreased Methylation capacity (the loss of cell viability/vitality), compounded by… 

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…

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 – it is a bell weather indicator.

   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-bacterium type “sludge”, 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… 

7. Subsequent underlying contamination of the “bedrock” gut (Yeast overgrowth, Gut Flora, Mycoplasma) which creates a perfect breeding ground for Leaky Gut Syndrome & ensuing Inflammatory Bowel Diseases (Celiac/Crohn’s Disease, Colitis); and further… 

8. Ensuing depletion of vital nutrients (trace minerals & anti-oxidants) from the body. Common deficiencies amongst children with  Autism frequently include: Vitamin A, B6/B12, C, D3, E, Glutathione, Selenium. These are the body’s 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.

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 “cholecalciferol” 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  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

Excerpt from VRM: The Autism Report


Breaking News: Childhood Influenza-Type Pneumonia Directly Linked to PCV Vaccine Bacterial Cross-infection  

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.

Note: ‘8 times more predisposed to a Methicillin-resistant Staphylococcus Aureus (MRSA) bacterial co-infection occurring in the lungs.’

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 – 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) –

…leaving 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

A recent study by the Centers for Disease Control and  Prevention (CDC) found that of the 36 children who died from H1N1 from  April to August (2009), six had no chronic health conditions. But all of them  had a co-occurring bacterial infection. The most common co-occurring  infection that causes flu-related deaths is staphylococcus aureus. A  third of the population carries it, most in their nose or on their skin.  The flu causes upper respiratory damage, which allows the staph to make  its way into the lungs.’ ‘Co-detection of Pandemic (H1N1) 2009 Virus and Other Respiratory Pathogens’, CDC

Note: ‘The most common viral pathogens in the pandemic (H1N1) 2009–negative  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)…The 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).’  Centres For Disease Control: Co-detection of Pandemic (H1N1) 2009 Virus and Other Respiratory Pathogens, December 2010

Clearly society has reached its saturation point with the widespread over-use of anti-biotics; which has given rise to the emergence of  ‘multidrugresistant staphylococci’, potentially the greatest of threats  to our natural immunity, in terms of its resilience in the environment & virulence in the human host. ‘Spontaneous chromosomal mutations have also played a role in the emergence of clinically important resistance‘…’It’s possible methicillin- resistant Staphylococcus aureiis will become untreatable.

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: 

Role of Staphylococcus aureus Catalase in Niche Competition against Streptococcus pneumoniae: ‘Nasal colonization by Staphylococcus aureus is a major predisposing factor for subsequent infection. Recent reports of increased S. aureus colonization among children receiving pneumococcal vaccine implicate Streptococcus pneumoniae as an important competitor for the same niche. Since S. pneumoniae uses H2O2 to kill competing bacteria, we hypothesized that oxidant defense could play a significant role in  promoting S. aureus colonization of the nasal mucosa. Using targeted mutagenesis, we showed that S. aureus expression of catalase contributes significantly to the survival of this pathogen in the presence of S. pneumoniae both in vitro and in a murine model of nasal cocolonization.

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

Note: ‘Recent reports of increased S. aureus colonization  among children receiving pneumococcal vaccine implicate Streptococcus pneumoniae as an important competitor for the same niche.’

‘Bacteria that cause childhood pneumonia and meningitis have  evolved to evade vaccines by swapping bits of their genome with other  bacteria, according to a new study. Vaccines that protect against these so-called pneumoccoccal infections are designed to recognise a material  on the outer surface of a bacterium’s cell called polysaccharide. Each of more than 90 kinds, or “serotypes”, of these bacteria have a different polysaccharide coating.

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

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

Note: ‘…the bacteria will continue to morph into new forms’.

This reformulating or “morphing” nature of the Staphylococcus   aureus-type pathogen is indicative of years spent being sliced and  re-spliced in top Level Bio-laboratories; while overcoming the body’s  natural  anti-biotic defenses through prolonged incubation in the host species –  increasingly compromised generation to generation by the over-use of  Prescription anti-biotics and vaccine derived heavy  metal/excipient/virus & bacterium “sludge” toxicity.
The  routine administering of post Influenza vaccination Prescription Drugs  (Vancomycin & Oseltamivir aka Tamiflu) led to serious adverse  interactions which not only hastened the critical conditions of those  who sought hospital care, but may, in fact, have triggered the premature deaths of most, if not all children who succumbed to 2009’s laboratory produced “novel” strain of H1N1 (2 parts Swine Flu, 1 part Human Flu, 1 part Avian Flu).

‘The detection of an increased number of A(H1N1) viruses with resistance to oseltamivir (Tamiflu)   was initially reported to WHO by Norway on 25 January 2008. The  viruses  carried a specific neuraminidase (NA) mutation (H274Y) that  confers  high-level resistance to oseltamivir in N1-containing influenza viruses. Prior to the recent report from Norway, such resistance was  rarely  observed in community isolates of influenza A or B. During the  previous  northern hemisphere winter season (2006/2007), surveillance through the Global Influenza Surveillance Network (GISN) laboratories found no oseltamivir-resistant H1N1 viruses among isolates from Japan or Europe, and less than 1% prevalence among H1N1 isolates from the United States of America.

The mutation in N1 neuraminidase of human influenza virus which confers high-level resistant to oseltamivir 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 corresponding amino acid in these subtypes is at position 274. Consequently, some scientists use ‘N2 numbering’ (H274Y) and some use the actual ‘N1 numbering’ (H275Y).’ WHO

The truth is the body is being systematically targeted  & broken down from all sides, creating a perfect storm of toxicity  which has derailed the inherent functionality of our natural immunity  generation to generation; thereby opening the door to widespread ill  health. Western medicine, however they spin its so called “progress”,  continually offers the antithesis of a natural solution.

It is no longer a coincidence to suggest a correlation between “natural vs. manufactured (prescription)” anti-biotic/anti-viral breakdown in the body and  “natural vs manufactured (prescription)” anti-biotic/anti-viral resistance overload proliferating in the environment. Approximately ‘2 out of every 100 people carry a strain of staph that is resistant to these antibiotics‘.   We have reached the saturation point as a species; with the continued   oversight of Western Allopathic Medicine, focusing solely on treating (and thereby exacerbating) symptoms rather than seeking out & remedying (embracing) the underlying cause.

‘Children with preexisting neurologic conditions and immune compromise were at increased risk of pH1N1-associated death after PICU admission. Secondary complications of pH1N1, including myocarditis (inflammation of the heart muscle), encephalitis (inflammation of the brain & meninges), and clinical diagnosis of early presumed MRSA (Methicillin-resistant   Staphylococcus Aureus) coinfection of the lung, were mortality risk   factors.’ Published in American Academy of Pediatrics, 09/31/11

There’s more risk for MRSA (methicillin-resistant Staphylococcus aureus) to become invasive in the presence of flu or other viruses. These deaths in co-infected children are a warning sign. This is especially alarming given the rising rates of MRSA infections being carried widely among children. It is not common in the U.S. to lose a previously healthy child to pneumonia. Unfortunately, these children had necrotizing pneumonia eating away at their tissue and killing off whole areas of the lung. They looked like immunocompromised patients in the way MRSA went through their body. It’s not that flu alone can’t kill – it can – but  in most cases children with flu alone survived…The more antibiotics we   take, the more we colonize ourselves with antibiotic-resistant organisms such as MRSA.” Adrienne G. Randolph, MD, Division of Critical Care Medicine at Children’s Hospital Boston

‘During the 2009 H1N1 influenza pandemic, many previously healthy children became critically ill, developing severe pneumonia and respiratory failure, sometimes fatal. The largest nationwide investigation to date of influenza in critically ill children, led by Children’s 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 healthy children. Moreover, almost all of these co-infected children were rapidly treated with vancomycin, considered to be appropriate treatment for MRSA. The fact that they died despite this treatment is especially alarming given the rising rates of MRSA carriage among children in the community.

While most of the children critically ill with H1N1 had one or more chronic health conditions that increased their risk, such as asthma, neurologic disorders or compromised immune systems, 251 children (30 percent) were previously healthy. Among these otherwise healthy children, the only risk factor that was identified for death from influenza was a presumed diagnosis of MRSA co-infection in the lung – which increased the risk for mortality 8-fold (P<0.0001). 88 percent of the children admitted to the ICU received Tamiflu (oseltamivir)    during their stay, but only 6 percent had received it prior to hospital admission…The study also found that most of the MRSA co-infected children who died had received vancomycin promptly at or before ICU admission.’ Children’s Hospital, Boston

Note: ‘88 percent of the children admitted to the ICU received Tamiflu (oseltamivir) during their stay…’

See VRM: The Flu Report

See VRM: PCV Vaccine Exposed – Breeding Ground For Staphylococcus Aureus


VRM Editorial: The Trans-humanist war against humanity

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’s retaliatory instinct. Natural immunity will have no place in this so called “brave new world”. The Trans-humanist Elites financing this dark revolution believe they will one day merge with the machine, in the wake of humanity’s orchestrated demise…a 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…and in the end Nature will once again prevail. VRM

One concern about nanotechnology’s 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.’ National Science Foundation: Societal Implications of Nanoscience and Nanotechnology

See VRM: The Rockefeller Foundation Drafts A Post-Pandemic Scenario

See VRM: Birth of Medical & Scientific Dictatorship – Future Scenarios

See VRM: Pandemic Preparedness & The Dark Agenda Ahead

See VRM: Morgellons Syndrome & Chemtrails


VRM Editorial: Architecture of The Human Body 

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.

The basement area of the house headquarters the central plumbing unit, including the primary “electrical grid” 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 “electrical grid” stations encasing the nerve center/brain of the human body (comprising the Blood-Brain barrier, Myelin sheath & Meninges).

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.

The interconnection (fluidity) of the “electrical grid” 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’s senses & warning signs – everything related to overall system co-ordination & metabolisim is managed via this delicate bio-conductive process.

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 – 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.

The synergy of vaccine derived heavy metal-virus-mycoplasma-excipient toxicity “sludge” targets the 3 primary core “electrical grid” stations encasing the nerve center/brain – 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 stage in early childhood development, neuro-developmental disorders such as Autism will inevitably follow in many instances.

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 “electrical grid” nerve center violated prematurely – all of which significantly inhibits the capacity of the body to carry out its normal systems of operation. The gut level “plumbing” crisis, a hallmark of Autism, is the end result of a “house” in crisis; ground zero for neurological & neuro-developmental disfunction.

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


VRM Editorial: Hospital Birthing vs. Home Birthing

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). 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.
‘Having worked in hospitals for over twenty years as RN, I can validate the “oversight” re. vaccine protocol.’ Viewpoint of a veteran Registered Nurse
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.
The 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 “programmed” 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’s delicate, under-developed “electrical grid system” (Myelin sheath, Meninges & Blood Brain Barrier).

 Official Package Insert: ‘10 µg/mL  Each 1 mL dose of sterile suspension contains hepatitis B surface antigen 10 µg adsorbed onto approximately 0.5 mg of amorphous aluminum hydroxyphosphate. Formaldehyde-treated. Thimerosal (mercury derivative) 1:20,000 (50 µg/mL) has been added only to the preservative-containing formulations. 3-dose vials of 3 mL‘…’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.

See: VRM: The Autism Report


Senior World Bank Globalist admits to Vaccination Campaign “targeted action”-type “Policy Levers” for ongoing Global Population Management (Bioethics aka Eugenics) Strategy
‘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’s 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 “policy levers” 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
Interview with John F. May concerning the demographic future of the planet (Sens Public), Center for Global Development, October 2, 2012
See VRM: The Problem With Vaccines Part 3 – Synthetic Genomics & The Death Of Natural Immunity

Recommended treatment for puncture wounds, cuts & lesions:

1. Apply Tea Tree Oil drops to exposed/infected area.

2. Apply Oil of Oregano drops to exposed/infected area.

3. Next, apply a generous mixture (balm) of Bee Propolis & Comfrey extract to exposed/infected (including burn related) area.  

4. Wrap in a non-toxic type gauze (for appropriate period – typically 2-3 days) to allow for natural, gradual healing process. 

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.

Repeat steps 1-4 if necessary, depending on the extent of the injury incurred. 

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 are indoctrinated with short-sighted Medical thinking and most often know nothing about the benefits of natural immunity.


VRM Editorial: On The Road To Natural Immunity

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.

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.

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’s 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 “experts”, are woefully mistaken. The ENTIRE Vaccine Industry is a fraud, period. All vaccines, by their very nature, play off each other – a “synergistic” 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.  

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 “threats”, rather than holistically EMBRACING all that we come in contact with, thereby re-enforcing, through HARMONY, the inherent properties of natural immunity. We’re 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 …and ultimately, a perfect environment for otherwise AVOIDABLE hybrid forms of cancer.

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’s 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?

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