Toxicity is defined in the Medical lexicon as “a condition that results from exposure to a toxin or to toxic amounts of a substance that does not cause adverse effects in smaller amounts.” Vaccine-induced toxicity, while similar in some respects to this model, requires a deeper understanding in terms of its overall effect on the human body.
Most practicing MD’s recognize Mercury & Aluminum to be severe neuro-toxins. Still, pediatricians & family doctors routinely recommend their patients (including babies, young children, pregnant women & the elderly) receive the full/partial schedule of standard immunization shots available.
How many of these doctors have examined the package inserts accompanying each vaccine? And if so how many have considered the synergy factor that occurs when combining multiple ingredients such as heavy metals, live viruses (or strands of DNA/RNA “heat treated virus”), mycoplasma, anti-biotics, formaldehyde, detergent, diploid cells, phenol dye & excipient buffers; their synergistic long-term impact on the body’s delicate network of immune, endocrine, nervous, circulatory, lymphatic & digestive system operations?
In a closed door meeting conducted by the CDC in 2000, doctors alluded to their concerns over heavy metal toxicity in vaccines; while acknowledging a glaring void in scientific research on this neglected aspect of synergy,
“Aluminum & mercury are often simultaneously administered to infants, both at the same site & at different sites. However, there is absolutely no data, including animal data, about the potential for SYNERGY, additively or antagonism, all of which can occur in binary metal mixtures that relate and allow us to draw any conclusions from the simultaneous exposure to these two salts in vaccines.” Dr. Johnson, P. 20
In the same breath Johnson also stressed the necessity of using aluminum as an adjuvant (immune stimulant) in vaccines,
“Aluminum salts are important in the formulating process of vaccines, both in antigen stabilization and absorption of endotoxin.” P. 19
“But from all of the other studies of toxic substances, the earlier you work with the central nervous system, the more likely you are to run into a sensitive period for one of these effects, so that moving from one month or one day of birth to six months of birth changes enormously the potential for toxicity. There are just a host of neurodevelopmental data that would suggest that we’ve got a serious problem. The earlier we go, the more serious the problem.” Dr. Weil, P. 24
“I got called out at eight o’clock for an emergency call and my daughter-in-law delivered a son by C-section. Our first male in the line of the next generation, and I do not want that grandson to get a Thimerosal containing vaccine until we know better what is going on. It will probably take a long time. In the meantime, and I know there are probably implications for this internationally, but in the meanwhile I think I want that grandson to only be given Thimerosal-free vaccines.” Dr. Johnson P. 200
These are glaring examples of medical hypocrisy in action – such rampant blind trust in long-held beliefs ingrained in medical students throughout their formal training; which thus extends in real practice to the clinics & hospitals we frequent as trusting patients.
Compare this to another professionally held viewpoint:
‘In 1927, Dr. Victor Vaughn, a toxicologist with the University of Michigan, testified before the Federal Trade Commission that “all salts of aluminum are poisonous when injected subcutaneously or intravenously”. According to the American Academy of Pediatrics, “Aluminum is now being implicated as interfering with a variety of cellular & metabolic processes in the nervous system and in other tissues. In 1997 The New England Journal of Medicine published data showing that premature babies injected with aluminum build up toxic levels in the blood, bones and brain, and that aluminum toxicity can lead to neurological damage, including mental handicaps at 18 months of age.” Neil Miller
This wide gulf in understanding can be explained. According to Dr. Russell Blaylock, world renowned former brain surgeon, the average doctor receives the equivalent of a weekend seminar, in their first year only, on the specific topic of the neurological side-effects & disorders associated with vaccine uptake; approximately seven hours of careful, focused study into the complex strata of auto-immune breakdown type complexities. Without this fundamental bedrock of knowledge a critical component is missing from any doctor’s arsenal, considering the widespread impact neurological side-effects to vaccines have had on the community at large.
‘No medical man during his student days is taught to think. He is expected to assimilate the thoughts of others and to bow to authority. Throughout the whole of his medical career he must accept the current medical fashions of the day or suffer the loss of prestige and place. No public appointments, no coveted preferments are open to the medical man who declines to parrot the popular shibboleths of his profession. His qualifications may be beyond reproach, he may in himself possess qualities that command respect, but unless prepared to think and act within the narrow circle of accepted dogmas, he must be prepared for a more or less isolated path.’ Dr. Walter Hadwen, M.D., UK
Precisely what is aluminum and why is it so deadly in terms of vaccines?
Aluminium: A silvery-white, ductile metallic element, the most abundant in the earth’s crust but found only in combination, chiefly in bauxite. Having good conductive and thermal properties, it is used to form many hard, light, corrosion-resistant alloys. Atomic number 13; atomic weight 26.98; melting point 660.2°C; boiling point 2,467°C; specific gravity 2.69; valence 3.
‘Aluminium is mined in huge scales as bauxite (typically Al2O3.2H2O). Bauxite contains Fe2O3, SiO2, and other impurities. In order to isolate pure aluminium, these impurities must be removed from the bauxite. This is done by the Bayer process. This involves treatment with sodium hydroxide (NaOH) solution, which results in a solution of sodium aluminate and sodium silicate. The iron remains behind as a solid. When CO2 is blown through the resulting solution, the sodium silicate stays in solution while the aluminium is precipitated out as aluminium hydroxide. The hydroxide can be filtered off, washed, and heated to form pure alumina, Al2O3. The next stage is formation of pure aluminium. This is obtained from the pure Al2O3 by an electrolytic method. Electrolysis is necessary as aluminium is so electropositive. It seems these days that electrolysis of the hot oxide in a carbon lined steel cell acting as the cathode with carbon anodes is most common.’
Aluminum is a highly conductive metal. Note the scientific description: “aluminium is so electropositive”. The human body is also charged with electromagnetic, bio-conductive energy. Essentially we are bio-electric beings. Certain storehouses are concentrated with higher degrees of “conductivity”; in particular the brain which consists primarily of neurons.
‘Under a microscope a neuron looks like an octopus with many tentacles. A neuron can transmit an electrical impulse to the next neuron. The network of electrical impulses enables us to receive information from the physical world and then send it to our brains, and vice versa. Without the neuron circuits our bodies would completely shut down, like turning off the power supply to a city. If it were possible to describe the nervous system as a circuit diagram, with each neuron represented by a single pinhead, such a circuit diagram would require an area of several square kilometres it would be several hundred times more complex than the entire global telephone network.’
Aluminum (Aluminum Hydroxide/Potassium Sulfate) use in vaccines traces back to the early 1920′s. Alum (Sodium Potassium Sulfate) had already been used in Industrial applications for generations, mainly as a fix-it in dyes. In new trials they discovered it would also generate a prolonged immune response when injected into the body as an adjuvant; whereupon aluminum was immediately introduced on the vaccine market. However no studies were done to ascertain its effects on the nervous system or behavior. The Regulatory Agencies quietly rubber stamped & fast tracked the product for approval, merely ‘grandfathering’ it into widespread use, without any precautionary clinical safety analysis. To this day, aside from Squaline (shark oil), aluminum remains the primary immune stimulating component in all ‘heat-treated virus’ type vaccines.
It is important to note Mercury use in vaccines was similarly rubber-stamped into service. ‘Invented in the 1920’s by Eli Lilly (Thimerosal is 49.6% ethlymercury by weight, a neurotoxin known to be more than a hundreds times more lethal to tissue than lead) safety testing consisted of a 1930 study of 22 patients dying from mengiococcal meningitis in an Indiana hospital. Patients were injected with the solutions and followed until their death, which was within days. Because the patients died of meningitis, they were declared to show no adverse reaction to thimerosal and the product was declared safe for use.’
Eli Lilly and Company: Thimerosal/Material Safety Data Sheet – ‘Thimerosal contains 49.6% w/w organically-bound mercury. Exposure Guidelines: Thimerosal – No known occupational exposure limits established. Early signs of mercury poisoning in adults are nervous system effects, including narrowing of the visual field and numbness in the extremities. Exposure to mercury in utero and in children may cause mild to severe mental retardation and mild to severe motor coordination impairment.’
‘A single thimerosal-containing vaccination produces acute ethylmercury blood levels of 10–30 nM (nanomolar concentration), and blood samples in 2-month-old infants, obtained 3–20 days after vaccination, contain 3.8–20.6 nM ethylmercury. Our studies therefore indicate the potential for thimerosal to cause adverse effects on MS (methionine synthase – determines the viability of cells) activity at concentrations well below the levels produced by individual thimerosal-containing vaccines.’ M Waly, H Olteanu, R Banerjee, S-W Choi, JB Mason, BS Parker, S Sukumar, S Shim, A Sharma, JM Benzecry, V-A Power-Charnitsky, RC Deth – See page 10
‘Autistic children have much lower Hg (Hemoglobin – Oxygen supplier/iron-containing oxygen-transport metalloprotein in the red blood cells) levels in their birth hair, yet numerous physicians have reported that autistic children carry a higher mercury body burden than control children. The obvious explanation is micro-mercuralism & genetic susceptibility to retention toxicity. There is an obvious gender difference. This is explained by testosterone (male sex hormone) effects on T-toxicity. Estrogen (female sex hormone) decreases Thimerosal toxicity (species defense mechanism equipped in female body) whereas Testosterone increases the toxicity. Gender effects are involved.’ Dr. Boyd E. Hayley
There is also a myth, perpetrated by the Vaccine Industry, suggesting the alternative use of a muted or heat-treated virus negates any direct infection of the immune system. ‘Attenuated or killed vaccines are not dead or neutral, since they must retain immunising power if they are to produce a reaction from the immune system. Their active principle is therefore to cause disease and insofar as the sought-after effect is to provoke the malady, vaccines represent a traumatizing jolt to the organism.’ Whether you’re receiving a live virus or so called “dead strands of RNA/DNA”, the adjuvant accelerates any lessening which may occur in tempering down the original virus. It is, in essence, super-charged, re-ivigorated by the metal salts or Squaline otherwise added to the concoction; generating a robust immune response.
Immune suppression has everything to do with point of entry into the body; in addition to the timing of exposure to these toxic elements. As mentioned in part one of this article, the vast majority of infections enter the body through the nasal passages (mucous membrane) & the Gastro-Intestinal Tract or the guts (gut flora). Accordingly 80% of the body’s immune system is stationed at these junctures – the first line of defence.
Vaccines are injected into deep muscle tissue, a route which literally bypasses one’s natural defences altogether. Inadvertently, heavy metals & live viruses that would otherwise be sequestered & chelated out of the body, will unnaturally accumulate in the bloodstream. The very young (babies and small children) are at a high risk because their brains are undergoing the most rapid development at the very time they receive the greatest number of vaccinations.
Early onset autism occurs anywhere from 12-18 months, potentially even earlier. It is significant that autism coincides precisely with most intense period of standard immunization. According to the CDC’S ‘Recommended Immunization Schedule for Persons Aged 0 Through 6 Years—United States • 2010′ by 15 months the average child has received 25 injections including: 3 doses of Hepatitis B, Rotavirus, HIB (Haemophilus Influenzae Type b), IPV (Inactivated Polio Vaccine) & Hepatitis A, 4 doses of DPT (Diphtheria, Pertussis, Tetanus) & PCV (Pneumococcal Conjugate Vaccine), 1 dose of Varicella & Meningococcal and 2 doses of MMR (Measles, Mumps, Rubella).
As Dr. Gary Tunsky illustrates, Aluminum is a coagulant which inherently binds to any toxin in its path. In fact its primarily industrial use is to bond debris in water treatment centers; whereupon it is then scraped out of the cylinders during the filtration process.
“Your blood has no method of excretion; Heavy metals & live viruses, formaldehyde are redistributed by the blood to areas of fatty tissue (highly conductive/electrical tissues) – found in the gray matter of the brain, the Myelin Sheath, neurons, the meninges/spine, cardiac cells, breasts & ovaries (in women), prostate (in men). Blood is made of water. When you stick aluminum in your blood, anything that’s toxic debris is going to bond to and coagulate and cause a congestive coccidiosis and this stuff gets caught in the tiny highways & byways. So you have the big gushing arteries & veins but they byfricate and branch into streams like a river; and they branch in again to the tiny arterial & capillary bits. That’s where the blockages are occurring, the brain, the spine, (the intestines/bowel) fingers & toes – which turn blue, choking of the micro-vessels from all the sludge that gets caught from all these repetitive hits/vaccinations, over & over. There are 60,000 miles of blood-vessels in one body. They run through every part of your muscle, your bone, your brain. Anywhere you stick an inter-muscular injection it goes into the blood. ” Dr. Gary Tunsky
Aluminum is a positively charged bio-conductive element, 64 times more positive than colloidal blood products (ie. anything suspended in your blood) are negative; with the properties of a coagulant. It literally draws in all other metals & toxins in its path. When injected into deep muscle tissue or subcutaneously, this neurotoxin gets redistributed via the bloodstream (consisting of 90% water) to areas of fatty tissue (highly electrical tissues – negatively charged) throughout the body, builds up over time in these delicate centers; primarily in the Brain, Spinal cord, Myelin sheath, Meninges, cardiac cells, breasts & ovaries (in women), prostate (in men), kidneys, liver, gut & bowels.
The viscosity of this toxic sludge resulting from vaccines which accumulates in the organs (ie. heart, liver, kidney, spleen), joints, meninges, intestines, along the neural pathways, veins & capillaries interlacing the entire body (resulting from “stagnant” blood), is comparable to the black paste-like build-up found over time in the lining of your drains – especially in terms of its impact on your vital health.
‘Approximately 25% of the total amount of the cholesterol present in humans is localized to this organ, most of it present in myelin. Almost all brain cholesterol is a product of local synthesis, with the blood-brain barrier efficiently protecting it from exchange with lipoprotein cholesterol in the circulation.
It has been estimated that up to 70% of the brain cholesterol is associated with myelin. Because up to half of the white matter may be composed of myelin, it is unsurprising that the brain is the most cholesterol-rich organ in the body. The concentration of cholesterol in the brain, and particularly in myelin, is consistent with an essential function related to its membrane properties.‘ Division of Clinical Chemistry, Huddinge University Hospital, Sweden
Within 72 hours of oxygen deprivation any cell can become cancerous. Cancer cells thrive in an oxygen-deprived environment. This will occur when bio-conductive aluminum (consisting of live virus, antibiotic, heavy metal, detergent coagulated sludge) clogs/singes the vast network of arterial veins & capillaries leading to the brain, inducing Ischemia.
‘Oxygen–glucose deprivation resulted in expression of apoptotic and necrotic cell death phenotypes, especially in neurons.’ ‘Following 72 hours incubation in the presence of 0.3% O2, cells were labeled with Annexin V/PI and the level of cell death was measured by flow cytometry. In 6 independent experiments, hypoxia increased levels of Annexin V-positive OC316 cells from 5.3 ± 1.0% to 19.2 ± 2.8%; …cell death under these conditions had predominant features of late apoptosis.’
Meanwhile bad food choices (casein, gluten, poly-saturated fats, iodized salts, sugars) produce a breeding ground in the body for long-term infections, thyroid disorder, disease & vaccine derived viruses. All viruses thrive in a non-alkaline, acidic environment. Overall the impact of of Ischemia & excessive alkalinity serve as a double-edged sword, critically damaging our vital health.
‘The human blood is a colloidal suspension. Proteins, Amino acids, heavy metals etc., are carried in suspension within the blood as a function of the net negative charge within the system. Drop the net negative charge, flow pressures in tiny end blood vessel “pipes” will start to sludge, agglomerate, and increase viscosity of blood in circumscribed microscopic vascular areas.
This “sludging” is activated when Aluminum (64 times more positive than colloidal blood products are negative) interacts with Hemoglobin in flow, in the negatively charged environment. This causes the negatively charged blood products to “attract” towards the larger, more massive positively charged Aluminum, causing clumping or “sludging”. This restricts blood flow, and it changes the Zeta Potential to change from -15mv (minus 15 milivolts) towards -10 mv (minus 10 milivolts), or possibly closer to zero. This is an increase in Zeta Potential, from a negatively charge towards neutral. (This is somewhat analogous to a change in state of water as it turns to ice – it’s a change in viscosity, affecting blood flow).
Agglomerates of sludged blood products cannot traverse microscopic blood vessels designed to carry oxygen transporting red blood cells, in single file. Capillary blood vessels oriented against gravity are uniquely susceptible. Forward blood flow momentum is a function of the negative charge and “spin” in fluid dynamics which keeps particles with mass separated from one another. For the brain, and body, this causes hypoxia (low oxygen), anoxia (no oxygen) and ischemia (impaired blood flow). This is bodily harm when vaccine induced.’ Dr. Andrew Moulden
‘It is well known and published in the scientific literature that combinations of two chemicals may be 10 times as toxic as either separately, or 3 chemicals 100 times as toxic…The levels of mercury Thimerosal in vaccines has been shown to be highly neurotoxic, but the effect was found to be much larger due to the synergistic effect with aluminum, which is also in most vaccines.
In an unpublished paper by Frank Hartman entitled, ‘Vaccination. Toxicity. Infection and Science’ Hartman proposed a plausible theory implicating aluminum toxicity as one of the prime agents in vaccines leading to intravascular coagulation. There are over 7000 references to the toxicity of aluminum, he noted. In regard to the procoagulant effects he quoted a simple experiment of making a mixture of flour and water (in which the flour readily goes into the solution). When one drop of an antiperspirant (contains aluminum) is added, the flour immediately clumps and settles to the bottom. Touching on areas of physics, Hartman went on to explain,
“All trace minerals, metals, inorganic materials, proteins and amino acids are held in suspension in liquids as microscopic and submicroscopic particles like dust particles in the air. The very small particles are called colloids. Colloids are held in suspension via a very slight electronegative charge on the surface of each particle. This charge is called a Zeta Potential. The ability of a liquid to carry material in suspension is a function of these minute electrical charges. As the electronegative charge increases, more material can be carried in suspension. As the charge decreases the particles move closer to each other and the liquid is unable to carry the same amount of materials. Calcium and heavy metals drop out first, adhering to the vessel wall or organ surface.
The quantity of positive and negative charges from chemical elements in suspension as colloids has a major effect on carrying capacity. Electropositive ions decrease carrying capacity while electronegative ions increase it. Elements with only one excess positive or one excess negative have little effect on suspensions. Elements with two positive or two negative ions (divalent) such as magnesium or beryllium (+2) have 3000 times more effect on coagulation or dispersion than elements with single ions. Elements with a valence of 3, such as aluminum (+3) and nitrogen and phosphorous (-3) have 6000 times more effect on carrying capacity due to the three extra positive charges. vaccines contain aluminum salts which greater exacerbate coagulation.‘ Excerpt from ‘Medical Veritas: The Journal of Medical Truth’ By Gary S. Goldman, Ph.D P. 133-134
Note: ‘Elements with a valence of 3, such as aluminum (+3), have 6000 times more effect on carrying capacity (sludging toxicity) due to the three extra positive charges.’
The United States Food & Drug Administration ‘Drug Labeling Regulations Guide’ states unequivocally,
“Aluminum may reach toxic levels with prolonged parenteral administration if kidney function is impaired. Premature neonates are particularly at risk because their kidneys are immature, and they require large amounts of calcium and phosphate solutions, which contain aluminum. Research indicates that patients with impaired kidney function, including premature neonates, who receive parenteral levels of aluminum at greater than 4 to 5 [micro]g/kg/day accumulate aluminum at levels associated with central nervous system and bone toxicity. Tissue loading may occur at even lower rates of administration.”
This means that for a 6 pound baby, 11-14 mcg would be toxic. The Hepatitis B vaccine given at birth contains 250 mcg of aluminum – 20 times higher than safety levels allow. Babies weigh about 12 pounds (5.5 kg) at 2 months of age when they receive 1225 mcg of aluminum from their vaccines – 50 times higher than safety levels.’
Currently children are getting 17 shots containing aluminum, a quadrupling of the amount given since the 1970’s. It is found in Hepatitis A, Hepatitis B, DTaP (diphtheria, tetanus, pertussis), Hib (Haemophilus influenzae type b), Pneumococcal & Gardasil (HPV) vaccines.
‘Since the 2002 gradual phase-out of the Thimerosal Mercury in vaccines, the use of aluminum has increased by 20%. Babies receive multiple doses of aluminum-containing shots. For example the Hepatitis B vaccine (Energix-B) is given at birth, 2 and 6 months of age. Each dose contains 250 micrograms (mcg) of aluminum. The DTaP shot (Infanrix) is given at 2, 4, 6, and 15 months. Each dose contains 625 mcg of aluminum. the Hib vaccine (Pedvax) is given at 2, 4, and 12 months. Each dose contains 125 mcg of aluminum. The Hepatitis A vaccine (Havrix) is given at 12 and 18 months. each dose contains 250 mcg of aluminum. Thus babies who follow the CDC immunization schedule are injected with nearly 5000 mcg (50 mg) of aluminum by 18 months of age.‘
Based on Dr. David Ayoub’s findings children, on average, receive 2-400 micrograms per vaccine, over a milligram of Aluminum; a concentration & dosage that is 10 – 20 times more toxic than Mercury. Multiple vaccines are far worse, over a 1000 micrograms on average for a triple set shot. Compounding the problem even more aluminum gets in during the manufacturing process. An indicator that the tools and/or machinery used are not properly monitored for safety.
Dr. Mehl Madrona stresses the considerable dangers inherent to all adjuvants – “The vaccine-adjuvant complex can interfere with the development and integration of the immune, nervous, endocrine, and other body systems leading to profound neurological damage. Even today, adjuvants and adjuvant formulations which combine both immunoenhancing capacity and low toxicity are lacking.”
There is scant scientific literature covering the link between vaccine induced Aluminum toxicity in the brain & Alzheimer’s Disease. However scientists, generally, do concur that vulnerability to aluminum toxicity naturally increases with age as the body’s defences weaken; a common denominator amongst those coping with the disorder. ‘In both human Alzheimer’s disease and aluminum encephalopathy of animals, changes are observed in neurofibrillary structures. We have found that brains from Alzheimer patients contain approximately 1.4 times the aluminum level found in a control series.’
‘Changes of some elements in rat’s tissues except nerve centre with both ovariectomy and chronic aluminum toxication and the effects of estrogen supplement: “The content of Al (Aluminium) in kidney increased. Chronic aluminum toxication make Si (Silicon) transfer to heart of ovariectomized rats, and facilitate Zn (Zinc) in heart transfer to other tissues.”‘
Dr. Russell Blaylock goes even further, suggesting that vaccine derived viruses linger in the organs for decades to a lifetime. After 50 years of prolonged subcutaneous exposure to aluminum the gradual slide toward auto-immune failure, including a host of disorders such as Alzheimer’s, seems inevitable.
“Heavy metals & viruses in vaccines cause abnormal development in brain, long-term changes that put a child at high risk of neuro-degenerative diseases ie. Parkinson’s & Alzheimer’s for the rest of their life; also they become hyper-sensitive to environmental toxins (Pesticides, Herbicides). Live viruses in vaccines are incorporated into your genetic material & passed on to your children.”
‘One such study, in which autopsied elderly were examined for the presence of the measles virus, found that 20% of the brains had live measles viruses and 45% of other organs were infected. These viruses were highly mutated, meaning that they could be just as potent as other measles viruses, but could be even more virulent. Worse, is that in most cases they cause a smoldering destruction of tissues without the obvious symptoms of infection, which has been shown in a number of studies.’ Dr. Blaylock
A mutagenic Measles virus strain commonly infects the bowels of children with Autism. Merck package insert: Measles, Mumps, Rubella vaccine – ‘M-M-R II has not been evaluated for carcinogenic or mutagenic potential, or potential to impair fertility.’
Vaccine derived toxicity triggers intense cytokine reactions in children with Autism – Neuroglial activation and neuroinflammation in the brain of patients with autism: ‘Active neuroinflammatory process in the cerebral cortex, white matter & cerebellum of autistic patients, marked activation of microglia & astroglia. Cytokine profiling indicated that macrophage chemoattractant protein (MCP)-1 & tumor growth factor-beta1, derived from neuroglia, were most prevalent cytokines in brain tissues.’
‘Aluminum is one of the most abundant elements in the environment. Some human exposure is unavoidable — daily intake is largely oral and averages 30-50 mg ( 1 ). Of this, no more than about 7 mg is expected to come from water, based on the maximum reported concentration of aluminum in drinking water ( 2 ) and the average consumption of 2 l water/day. Inhalation exposure is generally negligible, though it can be significant in some occupational settings, as described below. The contrast between widespread occurrence and relatively low intake underscores the importance of speciation in determining the bioavailability of aluminum, as this metal is of limited solubility in its environmentally occurring forms. Despite generally low exposures, the toxicity of aluminum, particularly to the nervous system, is of concern. Much research on aluminum in recent years has focused on its role in the etiology of Alzheimer’s disease (AD), but epidemiologic studies attempting to link aluminum with AD in drinking water have been inconclusive and contradictory.
Aluminum in pharmaceuticals has been reviewed by Yokel ( 22 ). Some over-the-counter pharmaceuticals such as antacids and buffered aspirin contain sufficient aluminum to increase the daily dose significantly. Many antacids consist of a mixture of Al(OH) 3 and other hydroxides, such as magnesium. Maalox Extra Strength tablets, for instance, contain 400 mg Al(OH) 3 and 400 mg Mg(OH) 2 . The recommended dose for relief from gastric discomfort is up to eight tablets per day; that is, 3.2 g Al(OH) 3 , or 1.1 g aluminum, which is a 30-fold increase over the average exposure from food and drinking water alone. Patients with renal insufficiency often take large quantities of aluminum-containing antacids to bind excess phosphate. The resulting AlPO 4 is insoluble, making the phosphate more easily excretable via the feces. Other potentially significant exposures, though likely to be short term, can occur through use of intravenous solutions: 10% calcium gluconate and 3 M potassium phosphate were found to contain 5.1 mg aluminum/g and 17 mg/g, respectively. Diphtheria-pertussis-tetanus vaccine, administered widely in the United States to children and adults, contains an aluminum adjuvant ( 18 ).
Note: “the toxicity of aluminum, particularly to the nervous system, is of concern”.
Neuro-scientist Dr. Christopher Shaw has conducted rigorous independent studies to ascertain the connection between between aluminum in vaccines and the prevalence of dead motor neurons in mice; with indications of massive cell disruption. He has conclusive evidence verifying his theory.
‘In the first study, mice were subjected at regular intervals to specific behavioral tests of motor and cognitive function, including wire mesh hang (2×/week), open field (1×/week), and water maze (1×/week) over a 6 months post injection period (see ). The order in which the animals were tested was randomized for each trial. In the second study, we conducted a more detailed behavioural examination based on the automated EthoVision system (Noldus Information Technology, Seattle, WA) employing a video camera and tracking software (Noldus EthoVision® 3.1). Individual movements of the mice were tracked for 5 min in an open field at weekly intervals. The software allowed for quantitative measurements of a variety of motor functions, including distance moved, percentage of time moving, velocity, and a variety of others. These latter experiments continued for 28 weeks following the last injections.
Only mice injected with aluminum hydroxide showed significantly increased Morin labeling of cells in lumbar spinal cord compared to the other groups (Fig. 2A–E). Similarly, only aluminum-injected mice showed the presence of abnormal tau protein in motor neurons in lumbar cord (Fig. 3). Other regions of the cord were not tested in the current studies for either Morin or tau protein.The multiple aluminum hydroxide injections of experiment 2 showed profound effects on motor and other behaviours as shown in Figs. 4 and 5. Multiple aluminum injections produced significant behavioural outcomes including changes in locomotive behaviour, (Fig. 4) and induced memory deficits on water maze tasks (Fig. 5). Other behavioural measures including muscle strength and endurance as measured by the wire hang and motor coordination and balance as measured by rotarod were not significantly affected.
We speculate that the observed neurotoxic effects of aluminum hydroxide in the present study arise by both ‘direct’ and ‘indirect’ pathways, some of which are cited above. Direct toxicity refers to the physical presence (or close proximity) of aluminum and its potential for initiating cell death pathways.
Accumulation of aluminum into the cytoplasm via cellular uptake mechanisms or diffusion could cause alterations in glutaminase and glutamine synthetase and easily alter the availability of the neurotransmitter glutamate . Aluminum acting to induce abnormal tau protein accumulation could also increase neurofibrillary tangles and impair cellular transport mechanisms . Outside the cell, aluminum could affect neurons by altering synapses. For example, aluminum has been shown to decrease the thickness of post-synaptic density, increase the width of the synaptic cleft, and increase the number of flat synapses . Aluminum could also block voltage-activated calcium channels , augment the activity of acetylcholinesterase , or interfere with synaptic transmission by merely accumulating in the synaptic cleft . Aluminum can also induce apoptosis in astrocytes . Since astrocytes are essential for maintaining neuronal health, any loss of astrocyte function could prove toxic to neurons. Indirect toxicity of aluminum could occur in various ways, including by activating various cytokines , releasing glutamate in an excitotoxic cascade, or by modifying various enzymatic pathways . In addition to the above actions specifically on neural cells, aluminum might act indirectly by stimulating abnormal, generalized immune responses. This is, in fact, what adjuvants are placed in vaccines to do in the first place. Adjuvant neurotoxicity could thus be the result of an imbalanced immune response. Rook and Zumla  hypothesized that multiple vaccinations, stress, and the method of vaccination could lead to a shift in immune response [56,57]. Aluminum hydroxide has previously been shown to stimulate a Th2-cytokine response [9, 58].’
Smoking gun Study liking Macrophalgic Myofascitis to Aluminum adjuvant toxicity from vaccines: “This is the first report linking the latter with either of these two conditions and the possibility is considered that the coincident aluminium overload contributed significantly to the severity of these conditions in this individual. This case has highlighted potential dangers associated with aluminium-containing adjuvants and we have elucidated a possible mechanism whereby vaccination involving aluminium-containing adjuvants could trigger the cascade of immunological events which are associated with autoimmune conditions including chronic fatigue syndrome and macrophagic myofasciitis.”
NOTE: “…aluminium-containing adjuvants could trigger the cascade of immunological events which are associated with autoimmune conditions including chronic fatigue syndrome and macrophagic myofasciitis.”
Aluminum, combined with other ingredients commonly added to vaccines, will trigger more rapid & profound cell toxicity. Mercury, another devastating neurotoxin & one of the few liquid elements, actually binds with hemoglobin, which is responsible for oxygen transport to the tissues. In addition it “inhibits the regulation of brain glutamate levels, triggers excitotoxicity, increases brain free radicals and lipid peroxidation products, inhibits critical brain enzymes, inhibits antioxidant enzymes and impairs DNA repair ability”.
Dr. Boyd E. Hayley performed a synergy experiment using aluminum hydroxide, mercury & neomycin (antibiotic associated with Kidney Failure, hazardous to a fetus):
A set of 100 healthy cells were exposed to Aluminum. All the cells died at a certain rate. Another batch of healthy cells were then exposed to Thimerosal Mercury. All the cells died at a comparable rate. A third test of this kind was conducted using Neomycin. All the cells died at a similar rate. Then Haley exposed a healthy set of cells to Aluminum & Thimerosal together. The cells died at twice the previous rate. Finally he combined Aluminum, Thimerosal & Neomycin under the same conditions.
Note: The results indicated a 75% acceleration in cell deaths when all 3 ingredients were combined.
Thimerosal Mercury in vaccines permanently damages tissue sensitivity - ‘Neonatal administration of a vaccine preservative, thimerosal, produces lasting impairment of nociception (awareness of tissue injury) and apparent activation of opioid system in rats. Present findings show that THIM (Thimerosal) administration to suckling or adult rats impairs sensitivity to pain, apparently due to activation the endogenous opioid system.’
Aluminum + Thimerosal = twice the toxic overload – ‘Mercury readily combines with aluminium to form a mercury-aluminium amalgam when the two pure metals come into contact. A small amount of mercury can “eat through” a large amount of aluminium over time, by progressively forming amalgam and relinquishing the aluminium as oxide.‘
Whereas Aluminum is the more dominant metal as a coagulant & in terms of its net charge on the body, Mercury is clearly the more corrosive element.
“A small dose of mercury that kills 1 in 100 rats and a dose of aluminum that will kill 1 in 100 rats, when combined have a striking effect: all the rats die. Doses of mercury that have a 1 percent mortality will have a 100 percent mortality rate if some aluminum is there.” Donald Miller, M.D. Professor of Surgery, University of Washington
Formaldehyde, yet another common additive in vaccines ( used as “a preservative & disinfectant”, linked to cancer & chronic bronchitis) can cause proteins to irreversibly bind to DNA.
3 separate ingredients, each with the properties of a binding agent or coagulant.
a) Aluminum is a coagulant which inherently binds to any toxin
b) Ethyl Mercury (Thimerosal) binds with hemoglobin
c) Formaldehyde causes proteins to irreversibly bind to DNA
How is it possible scientists have overlooked these obvious hazards to neurological & physiological functioning? The overwhelming body of evidence suggests a much darker agenda afoot behind the veil of public policy-making.
Remember, aluminum saturates/coagulates with any toxin in its path, upon entry to the bloodstream via deep muscle tissue. Ethyl Mercury traps hemoglobin, which triggers Ischemia, (a singeing of the neural pathways from toxic overload which prevents vital oxygen from reaching the brain, literally inhibiting normal development; a form of suffocation); while Formaldehyde, a known carcinogen, causes proteins to irreversibly bind to DNA. In essence live/attenuated viruses and other powerful toxins literally piggy back in to these centers without any resistance (disabling most kidney & liver functionality along the way) via the “bully” catalyst, aluminum, coupled with the back door point of entry into the body – past the primary line of natural defences.
Given the vulnerability of babies & young children, with an under-developed blood barrier on the brain & Myelin Sheath (to which aluminum binds due to its composition of electrical tissues), the paths leading to autism, schizophrenia, chronic allergies & a myriad of other disorders & viral infections become increasingly apparent.
Neomycin & Polymixin B are antibiotics associated with Kidney failure; both hazardous to a fetus. They carry serious side effects, predominantly kidney failure. Neomycin is in the FDA pregnancy category D. This means that it is known to be harmful to an unborn baby. In the “first tier” of candidates to receive this unregistered, unapproved vaccine, pregnant women are on top of the list. Once again a case of gross negligence, endorsing the use of a toxic product in influenza vaccines recommended for Pregnant women, in light of this stern FDA warning,
Additionally, Polysorbate 80 or ‘Tween 80‘ is a type of detergent stabilizer commonly found in vaccines; which is linked to infertility & severe allergic reactions (ie. Anaphylaxis). ‘Neonatal female rats were injected with Tween 80 after birth. Treatment accelerated maturation, prolonged the oestrus cycle & induced persistent vaginal oestrus. Ovaries were without corpora lutea & had degenerative follicies.‘
Based on this verifiable clinical data no such toxin should ever, under any circumstances, be injected into a pregnant woman. Despite such conclusive evidence of its implications on female fertility, Polysorbate 80 is, in fact, added to many current vaccines including: HPV (Gardasil/Cervavix), DTaP (Infanrix, Tripedia), DTaP-IPV (Kinrix), DTaP/Hib (TriHIBit), DTaP-HepB-IPV (Pediarix), DtaP-IPV/Hib (Pentacel), Hep A (Havrix). 2009′s H1N1 ‘Swine Flu’ vaccine (produced by GlaxoSmithKline (Pandemrix/Arepanrix), Novartis (Focetria) & Baxter Pharmaceuticals (Celvapan), widely promoted as a mandatory safety precaution for ALL pregnant women, contained this ingredient; yet another glaring red flag to be considered.
“Polysorbate 80 was identified as the causative agent for the anaphylactoid reaction of nonimmunologic origin in the patient. Polysorbate 80 is a ubiquitously used solubilizing agent that can cause severe nonimmunologic anaphylactoid reactions.” Department of Dermatology, University of Aachen, Aachen, Germany
Specific role of polysorbate 80 coating on the targeting of nanoparticles to the brain (causes a blood/brain barrier breach) “Partial coverage was enough for Tween-80 coating to play a specific role in brain targeting of nanoparticles; concerned with the interaction between T-80 coating and brain micro-vessel endothelial cells. Therefore, the specific role of T-80 coating on nanoparticles in brain targeting was confirmed.” Department of Material Science and Engineering, Huazhong University of Science and Technology, China Study, 2003
To reiterate: 2 separate ingredients, either which contribute to an increased likelihood of infertility.
a) Neomycin/Polymixin B - antibiotics associated with Kidney failure; both hazardous to a fetus. “There is evidence to indicate that exposure to Neomycin during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects.’
b) Polysorbate 80/Tween 80 – detergent stabilizer commonly found in vaccines; which is linked to infertility & severe allergic reactions (ie. Anaphylaxis). “Delayed effects of neonatal exposure to Tween 80 on female reproductive organs in rats.”
The mother’s placenta, & breast milk (Colostrum) are inextricably linked, providing a baby’s primary initial source of nourishment through the long journey of formation in utero; while supplying the basic building blocks of life necessary to guarantee a safe transition into early childhood development. It seems almost inconceivable given the scientific literature in circulation, but somehow the CDC, WHO & local health authorities in countries around the world have begun vehemently recommending all pregnant women & babies as young as 6 months receive the seasonal flu vaccine during first trimester. It is common knowledge in medical circles that Thimerosal crosses not only the blood barrier into the brain, but also gets absorbed into the placenta when introduced to the bloodstream. Their justification borders on attempted infanticide.
Long-term implications of mercury exposure at this stage include Down’s Syndrome, early onset Autism, Lupus, Schizophrenia & a host of other chronic disorders & allergies (ie. Hyperbetacarotenemia, a form of intestinal disfunction linked to Measles marked by excessive beta-carotene in the blood & Vitamin A depletion).
‘The Advisory Committee on Immunization Practices (ACIP) recommends that pregnant and postpartum women receive the seasonal influenza vaccine this year, even if they received 2009 H1N1 or seasonal influenza vaccine last year. Influenza vaccine can be given to pregnant women in any trimester. Postpartum women, even if they are breastfeeding, can receive either type of vaccine. Administer annually to children aged 6 months through 18 years.’ CDC
It should come as no surprise that many pregnant women reported miscarriages during 2009′s H1N1 vaccination campaign. Of those who received the shot upwards of 3,600 cases of miscarriages and stillbirths have been reported, based on current estimates. Bare in mind that figure represents only approximately 10% of the overall numbers. Meaning only 10% of cases are ever reported officially. That translates to upwards of 30,000 possible vaccine induced miscarriages having actually occurred in the US alone.
‘A shocking report from the National Coalition of Organized Women (NCOW) presented data from two different sources demonstrating that the 2009/10 H1N1 vaccines contributed to an estimated 1,588 miscarriages and stillbirths – as high as 3,587 cases. Studies conducted by the CDC have been shown to miss from 10% to 90% of the actual cases because of under-reporting.’
‘Studies of the organs and tissues of the first generation progeny revealed mercury in the stomach and intestine at birth and in the first week of life, apparently on account of the entry of mercury through the placental barrier and by way of their mother’s milk. Subsequently, it was noted that the first-generation progeny of mothers that had been previously exposed to the ethyl mercury compound had significantly reduced fertility in comparison to controls. The second generation progeny had low viability, lagged in their weight growth, and were retarded with respect to ossification in several cases. Finally, it was then observed when mating the second generation progeny that there was a significant decrease in fertility in comparison to the control group.’
Note: Soy formula (typically GMO) is never a viable alternative to colostrum; as it is found to be ‘nutritionally inadequate and contain Manganese (Mn) at levels which may present an increased risk of adverse neurological effects if used as a sole source of nutrition‘.
Methylation assists in a critical stage of early development involving the viability of cells. ‘an on/off switch that allows the body to learn how to respond to environmental change. It represents the only cellular pathway that effects both adaptability and structural integrity of the body. Like the simple water molecule, methyl groups are necessary for life. This pathway is directly related to most major chronic conditions.’ Heavy metal toxicity breaks down this vital operation; yet another primary culprit in the eventuality of autism.
‘Methylation events play a critical role in the ability of growth factors to promote normal development. Neurodevelopmental toxins, such as ethanol and heavy metals, interrupt growth factor signaling, raising the possibility that they might exert adverse effects on methylation. We found that insulin-like growth factor-1 (IGF-1)- and dopamine-stimulated methionine synthase (MS) activity and folate-dependent methylation of phospholipids in SH-SY5Y human neuroblastoma cells, via a PI3-kinase- and MAP-kinase-dependent mechanism. The stimulation of this pathway increased DNA methylation, while its inhibition increased methylation-sensitive gene expression. The ethylmercury-containing preservative thimerosal inhibited both IGF-1- and dopamine-stimulated methylation with an IC50 of 1 nM and eliminated MS activity. Our findings outline a novel growth factor signaling pathway that regulates MS activity and thereby modulates methylation reactions, including DNA methylation. The potent inhibition of this pathway by ethanol, lead, mercury, aluminum and thimerosal suggests that it may be an important target of neurodevelopmental toxins.’ Molecular Psychiatry (2004)
Vaccines, by their very nature, play off each other – a synergistic 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.
Prevnor, for example, a childhood vaccine designed to “prevent” invasive pneumococcal disease (administered in 3 doses to 7-11 year olds not only doesn’t work, but also opens the reactive door to other crossover infections & diseases from vaccines given simultaneously during this age phase. Resulting cross reactions include Polio, Whooping cough, Diphtheria, Measles, Meningitis, Pneumonia, Chicken Pox & all varieties of chronic allergies ie. ear infections etc.
‘The vaccine schedule for infants(‘Prevnor’) is three doses at least one month apart, followed by a fourth dose at 12 to 15 months. It can be given at the same time as other vaccines but in a different site. For children 7 to 11 months of age, 3 doses are recommended, with the first 2 at least 1 month apart, followed by a third dose after the one-year birthday. For children 12 to 23 months of age, 2 doses are required at least 2 months apart, and 1 dose is required for children from 2 to 5 years of age.’
‘The efficacy of Prevnar appears to be very limited – 7% fewer new earaches, and 0.1% fewer instances of invasive pneumococcal disease (compared to an experimental vaccine used as a control). Prevnar Interferes With Other Childhood Vaccines The studies done on Prevnar suggest that it may interfere with the efficacy of two other vaccines (pertussis and IPV ‘Inactivated Polio Vaccine’) and could interfere with two more vaccines (MMR and Varicella).
According to the American Academy of Pediatrics: “Available data suggest that PCV7 (i.e. Prevnar) may prove to be among the most reactogenic (e.g., local reactions and incidence of fever) vaccine of those currently used, including the DTaP and Haemophilus conjugate vaccines.”36′
‘The pneumococcus bacteria cause infections that lead to the following diseases – meningitis, bacteraemia, pneumonia and otitis media.’
Government data admits to a probable causal link between vaccines & the presence of Measles in the bowels of young children (related to Inflammatory Bowel Disease); while promoting a deliberate cover-up of these inherent risks to the general public,
‘That Crohn’s disease and other chronic inflammatory illnesses of the intestine might be caused by a virus such as measles is an interesting hypothesis. Until the present time, microbiologic and epidemiologic arguments either for or against this hypothesis have not been very convincing. It is not very likely that other epidemiologic studies will provide conclusive evidence. In fact, it would be difficult to find a population that includes both individuals who have been exposed to the virus or to the vaccine and individuals who have not been exposed. However, new microbiologic studies might prove conclusive.
First, it would be necessary to demonstrate that the measles virus is indeed present in the lesions, that it is active, and that it contributes to inflammatory responses. Also, it would be necessary to prove that the pathogenic reaction can be induced by the wild virus and by the attenuated viruses present in vaccines. Strains and attenuation procedures vary from one manufacturer to another, and it is far from certain that all strains have the same ability to persist in tissues and to subsequently produce chronic inflammations. As was stated above, measles vaccine does not seem to be associated with SSPE, although the wild virus may be isolated (with difficulty) in patients with SSPE. The measles virus was isolated neither in patients with Crohn’s disease or other chronic inflammatory diseases (Paget’s disease, active chronic hepatitis, multiple sclerosis) in which a role for it has been claimed on morphologic, histologic or serologic grounds.
Current scientific data do not permit a causal link to be drawn between the measles virus and chronic inflammatory bowel diseases. While awaiting production and publication of other research, it would not be appropriate to alarm recipients of the vaccine by notifying them of this hypothetical risk, thus jeopardizing an immunization program of proven benefit.’
Scandalous cover-up: “…it would not be appropriate to alarm recipients of the vaccine by notifying them of this hypothetical risk, thus jeopardizing an immunization program of proven (cost) benefit.”
“We know in the world of infectious disease, that when women develop certain infections during mid term & later term of pregnancy (second & third trimester) they have a higher instance of having a child born with & developing autism or later in life, schizophrenia. that’s been known & shown in animal & in human studies. If you vaccinate pregnant women you’re significantly elevating their immune reaction. and the studies, as I began to look at this phenomenon, first they thought the mother was infecting the baby while the baby was in the uterus. Then they found out actually the virus never gets through the placenta so the baby’s not effected at all. It’s the immune reaction in the mother and these immune cytokines, these immune chemicals, that pass through the placenta into the baby that’s causing the baby’s brain to develop abnormally. So any immune stimulation of the mother can produce abnormalities in the baby with no virus whatsoever. And that’s what they proved experimentally. You could just stimulate the immunity with no infectious agent and still get high autism & schizophrenia.
If you run the risk of getting the flu during this season your risk is about 300′s of 1/1000th of 1% for a pregnant woman. In other words you have a 99.97 – 99.99% chance that you’re not going to end up in the hospital sick from the flu. And that’s by their own statistics. If you get the vaccine, and they give it to all pregnant women, then that means 100% of women have had a powerful immune stimulation during this critical period of brain formation of their baby. So that puts every woman at risk of having a baby born with high risk of autism or schizophrenia. And we’re talking about, according to the data we have, an increased risk of about 7 fold to as much as 14 fold (incidence of autism & schizophrenia in babies), a tremendous increase, depending on how much you stimulate the immune system. Other studies have shown it increases the baby’s risk of being susceptible to seizures early in life or even later in life, neuro-developmental problems, behavioral problems, all these subtle things.” Dr. Russell Blaylock
“The mechanism by which the immune system is corrupted can best be realized when you understand that the two poles of the immune system (the cellular and humoral mechanisms) have a reciprocal relationship. Thus, when one is stimulated, the other is inhibited. Since vaccines activate the B cells to secrete antibody, the T cells are subsequently suppressed. This suppression of the cell-mediated response is a key factor in the development of cancer and life threatening infections. In fact, the “prevention” of a disease via vaccination is, in reality, an inability to expel organisms due to the suppression of the cell-mediated response. Thus, rather than preventing disease, the disease is actually prevented from ever being resolved. The organisms continue circulating through the body, adapting to the hostile environment by transforming into other organisms depending on acidity, toxicity and other changes to the internal terrain of the body. Thus, treatment of infection with antibiotics as well as “prevention” of disease with vaccines are both just corrupted attempts at cutting off the branches of dis-ease, when the root of the cause is a toxic internal environment combined with nutritional deficiency.” Dr. Rebecca Carley, M.D.
What sort of a legacy are we leaving behind for our children, when the very health they depend on is compromised, if not crippled, by vaccines? The wisdom of our ancestors can be reawakened and passed on to our progeny. Before the Industrial Revolution the primary threat to one’s existence was always poor hygiene, poor sanitation, poor nutrition. We have now entered a darker phase in human evolution, in many ways a regression back to the Middle Ages in terms of the treatment of the masses by the few. The Medical Establishment clearly values profit-making over enhancing the quality & longevity of life. Our Governments have seen fit to broker secret, binding deals with the World Health Organization & Vaccine Manufacturers, to the detriment of our safety & inherent, natural-born rights. We are seemingly headed toward a nightmare scenario, soon to be stripped of our fundamental privilege to choose, to determine for ourselves & our families what goes into our bodies. The only hope is to make it our primary goal to secure forever our sacred rights to self-determination of the body. This will depend on us taking a stand against whichever form of tyranny that threaten these fundamental freedoms.
There will indeed come a day when vaccination, vivisection, & irradiation will have gone the way of the dinosaur, replaced by non-invasive, genuinely holistic techniques; when Allopathic-type medicine, along with all the ancient tools of its trade, will crumble in the wake of an evolution of consciousness & common sense; when Cancer, Autism, Aids & other encompassing afflictions will have become but a reference footnote in history. Godspeed & good riddance, as they say.
VRM LAUNCHES WORLDWIDE AUTISM STUDY:
The purpose of this worldwide study is to determine the incidence/rate of autism amongst those unvaccinated children & adults surveyed. We are also concurrently tracking the incidence/rate of autism amongst those vaccinated children & adults surveyed; cross-referencing dietary factors, pre-existing medical conditions/allergies, family health/vaccine history (multiple generations), breast/bottle feeding,
We hope to gain new insights into the causality & manifestations of autism with an exhaustive, scientific approach. Just to clarify this study is open to EVERYONE. The absence of autism in your family/household or the fact you haven’t vaccinated your children does not preclude you from taking part in the study. The control parameters are wide open this time. All the data we receive will be pertinent in determining the paths that lead to autism. VRM will be continuing to collect your invaluable data for as long as possible. That being said we still encourage everyone to enroll in the study while it’s openly available. Direct link to study: http://study.vaccineresistancemovement.org/
VRM: The Autism Report http://vaccineresistancemovement.org/?p=10185
VRM Worldwide Autism Study http://vaccineresistancemovement.org/?page_id=5463
VRM: The Problem With Vaccines Part 1
VRM: Vaccine Clinic – A Concise Compendium To The Problem With Vaccines
VRM: The Problem With Vaccines Part 3 – Synthetic Genomics & The Death Of Natural Immunity
VRM: A Concise Compendium To The Problem With Vaccines Part 3 – Synthetic Genomics & The Death Of Natural Immunity
VRM: The Problem With Vaccines Part 4 – Primary Aspects of Vaccine Toxicity Affecting Body
VRM: The Problem With Vaccines Part 5A – Detoxification & Restoration of the Body
VRM: The Problem With Vaccines Part 5B – Detoxification & Restoration of the Body
VRM: PCV Vaccine Exposed – Breeding Ground For Staphylococcus Aureus
VRM: The Rise of Mutagenic Viruses http://vaccineresistancemovement.org/?p=13124
VRM: Pandemic Preparedness & The Dark Agenda Ahead http://vaccineresistancemovement.org/?p=9460
VRM: Mandatory Vaccinations – How They Will Be Implemented http://vaccineresistancemovement.org/?p=11806
VRM: The Confidential Case-files of GlaxoSmithKline – Cover-up, Deferral & Denial of Responsibility for Vaccine-related Premature Deaths http://vaccineresistancemovement.org/?p=12242
VRM: Primary Reasons Not To Get The Flu Shot http://vaccineresistancemovement.org/?p=12642
VRM: The Flu Report
VRM: Vaccine Ingredients
VRM: Family Charts Gradual Decline Of Daughter
VRM: Pregnancy Tips
VRM: The Vanishing Sperm Count
VRM Live – 01/28/11: Vaccine Resistance Movement founder Joel Lord discusses Synthetic Genomics, cloned cell vaccine technology & the death of natural immunity, gutter journalism & Dr. Wakefield’s imminent vindication with ‘Truth to Power’ host Paul Mabelis.
VRM Live - 11/04/10: Vaccine Resistance Movement founder Joel Lord lays out the whole vaccine process with Paul Mabelis; including heavy metal toxicity, synergy, pregnancy issues & the basic principles of natural health at risk.
VRM Live - 09/24/10: Vaccine Resistance Movement Founder Joel Lord & activist/radio host Jesse Calhoun lay it all out tonite. Topics include the VRM Worldwide Autism Study, Scientific/Medical dictatorship, Natural Rights & Vaccine Industry fraud exposed. Special thanks to host Paul Mabelis.
If you appreciate the efforts to bring this information forward do consider making a donation. Any amount, no matter how small will help enable me to carry on this invaluable research. See Paypal link on the VRM website (click on ‘Donate’ tab in upper right corner). Thank you all.