Factors determining the extent of vaccine derived neurological damage:
1. POINT OF ENTRY
Vaccines are injected into deep muscle tissue/subcutaneously, either route which literally bypasses one’s natural defences altogether. Thus the body is left vulnerable to multiple live viruses, heavy metals, antibiotics, detergent & other additives found in the shots. The vast majority of infections enter the body through the nasal passages & the Gastro-Intestinal Tract or the guts. that’s where 80% of the body’s immune system is situated – at these junctures; so that’s your first line of defense. These ingredients get a backdoor entry into the most vulnerable areas of the body, in particular to the Brain & Spinal Cord. They also target vital organs such as the Kidney & Liver; which also inhibits the body from fighting back & building up any kind of healthy immune response. Your Kidneys are designed to flush toxins out of your blood, while the Liver sequesters & chelates heavy metals & other debris from your system.
Your last guard is essentially neutralized over time by this vast accumulation of toxicity.
2. TIMING OF INJECTIONS
Timing is CRITICAL. A baby has no blood barrier in the brain – so that vital, unfinished area is still completely raw. The Myelin Sheath, a casing or insulator which protects the baby’s basic cells, is also under-developed. Early onset autism, which occurs anywhere from 12-18 months, coincides precisely with most intense period of standard immunization. By 15 months the average child in most developed countries, has received a minimum of 25 injections. This results in severe heavy metal toxicity interfering with the earliest stage of development, during the first 6 months after birth.
CDC quotes from 2000 secret meeting: “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
“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. Johnston
Common deficiencies amongst children with Autism frequently include:
a. Vitamin A
b. Vitamin B6/B12
b. Vitamin C
c. Vitamin D3
d. Vitamin E
g. Mitochondria (related)
These are the body’s primary antioxidants (excluding Mitochondria), essential to regulating Free Radicals (unpaired Electrons) throughout the body, staving off Cancer, Diabetes, Autism, Schizophrenia & the rapid macro-degeneration of cells.
a. Hyperbetacarotenemia, a form of intestinal disfunction linked to Measles (from the MMR shot) is marked by excessive beta-carotene in the blood & Vitamin A depletion. Studies conducted in 1958 and 1961 confirmed that the wild measles virus has a severe short-term effect on immunity and the child’s nutritional status, especially vitamin A which is obliterated by the intervention of such a virus. Vitamin A plays a central role in the development & differentiation of white blood cells, such as lymphocytes, which are essential to the immune response. Vitamins C & E are dependent on Vitamin A. Therefore the bedrock of your immunity is compromised.
b. Starved of Vitamin D3: As a result the Lymphocytes in their lungs can’t process Vitamin C & E, which leads to Respiratory disfunction & increased vulnerability to ALL infections. Vitamin D is required to increase the circulation of calcium and phosphorous, two minerals necessary for healthy bones. The kidneys produce Vitamin D3 & the liver plays a vital role in the functioning of D3 throughout the body. When these organs are compromised , it will throw your entire metabolism off.
c. Many autistic children have a deficiency of Vitamin B6/B12, which is vital for the proper functioning of the brain and nervous system.
d. Estrogen protects the female brain from being damaged by heavy metal toxicity (including low Vitamin D). Testosterone, the male sex hormone increases heavy metal toxicity; explaining why Autism is statistically occurring 4-1 in boys over girls. “Autism is caused from a quantitative variation in one of the enzymes that metabolize Vitamin D.” Dr. John Cannell
e. Vitamin C is required for the synthesis of collagen, the inter-cellular “cement” substance which gives structure to muscles, vascular tissues, bones, tendons and ligaments. Vitamin C is also able to regenerate Vitamin E but not when the Vitamin D3 levels drop off.
f. Vitamin E is an antioxidant which intercepts free radicals and therefore prevents lipid destruction chain reactions. It maintains the integrity of cell membranes. After reactions with free radicals the antioxidant function of vitamin E is lost. Vitamin C is able to regenerate Vitamin E levels but not when the Vitamin D3 levels drop off.
g. Heavy metals rapidly deplete Selenium in the body. Selenium is necessary for Glutathione production (the body’s primary antioxidant). This causes a chain reaction which triggers liver damage, diabetes, cancer & in the long term, heart failure.
h. The Thyroid gland is key to overall health which produces T3 & T4 hormones (Iodine Atoms). Iodine helps regulate metabolism in the body. Thyroid synthesizes vital T3 (rare) from T4 (plentiful). Body needs 150 mg per day – 80% comes from T4 conversion to T3 in the Liver. Vaccine derived heavy metal toxicity neutralizes this function.
i. Damage to the Methylation process – 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.
j. Anti-mitochondrial antibodies are elevated; which suffocates Eukaryotic cells (complex structures enclosed within membranes). Mitochondria are the battery pack of your cells. “Mitochondria play an important role in controlling the life and death of a cell. Consequently, mitochondrial dysfunction leads to a range of human diseases such as ischemia-reperfusion injury, sepsis, and diabetes.” Most Eukaryotic cells contain other membrane-bound organelles such as mitochondria, chloroplasts & Golgi body. “Primordial eukaryotic cells lacked ability to use oxygen” – excerpt/Autistic case file.
These primary antioxidants are all interdependent, without which your fundamental metabolism is seriously compromised; a hallmark of Autism and a wake up call to those of us more fortunate:
Vitamin A plays a central role in the development & differentiation of white blood cells, such as lymphocytes, which are essential to the immune response.
Group B vitamins can act individually or in combination with the cellular enzymes to form vitamin B co-enzymes. These vitamin B co-enzymes are crucial to the metabolic pathways that generate the energy from carbohydrates, fat and protein, needed by every cell in the body. Vitamin B6 (pyridoxine) is required for the synthesis of the neurotransmitters serotonin & norepinephrine and for myelin formation. ‘In some experiments on chick growth with wholly vegetable diets supplemented with pure vitamin B12, a relationship became evident between the growth-stimulating effect of this vitamin and the content of calcium, iron and vitamin D of the diet.’ Vitamin D insufficiency has now reached epidemic proportions, firmly linked to increased body fat and decreased muscle strength.
Vitamin C is required for the synthesis of collagen, the inter-cellular “cement” substance which gives structure to muscles, vascular tissues, bones, tendons and ligaments. Vitamin C is also able to regenerate Vitamin E but not when the Vitamin D3 levels drop off. Vitamins C & E are dependent on Vitamin A. Therefore the bedrock of your immunity is compromised.
Vitamin D is required to increase the circulation of calcium and phosphorous, two minerals necessary for healthy bones. The kidneys produce Vitamin D3 & the liver plays a vital role in the functioning of D3 throughout the body. When these organs are compromised , it will throw your entire metabolism off. The Lymphocytes in your lungs depend on Vitamin D3 (steroid hormone derived from sunlight); without which they can’t process Vitamin C & E.
Vitamin E is an antioxidant which intercepts free radicals and therefore prevents lipid destruction chain reactions. It maintains the integrity of cell membranes. After reactions with free radicals the antioxidant function of Vitamin E is lost.
Selenium is necessary for Glutathione production (the body’s primary antioxidant). This causes a chain reaction which triggers liver damage, diabetes, cancer & in the long term, heart failure. Heavy metals rapidly deplete Selenium in the body.
Mitochondria is the battery pack of your cells which determines the body’s inherent ability to function efficiently; without which none of these connections are possible. Anti-mitochondrial antibodies are elevated in children with Autism; a process which suffocates Eukaryotic cells (complex structures enclosed within membranes). Vaccine derived heavy metal-antibiotic-detergent-virus sludge targets the body’s Mitochondria, while neutralizing major anti-oxidants throughout, causing Ischemia.
So you’re seeing a chain reaction affecting 7 major antioxidants in the body, all essential to regulating your overall metabolism, Liver, Kidney, Thyroid, Methylation, including Mitochondrial function, generally neutralized in these children with Autism; and all the evidence points to heavy metal toxicity derived from standard Immunization Vaccines (25 injections by 15 months).
Note: All vaccinated children, regardless, are susceptible to this depletion to lesser or greater extent.
Unlocking the keys to natural immunity requires a holistic approach to the complex functioning of the body. Every major organ & gland 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 & compromised immunity. Case in point, the Liver converts Vitamin D3 (cholecalciferol) into Calcidiol (25-hydroxycholecalciferol – aids in prevention of chronic Liver disease, Thyroid disorders, Diabetes, Cancer), from which the kidneys generate Calcitriol (active form of Vitamin D designed to increase calcium levels in the body in order to treat skeletal and tissue-related calcium deficiencies caused by kidney or thyroid disorders).
‘The liver and kidney have important enzymes that change vitamin D from the sun or food to the biologically active form of vitamin D. People with chronic kidney and liver disease are at increased risk of low vitamin D because they lack these enzymes.’
‘Calcitriol (1,25-dihydroxyvitamin D or 1,25(OH)2D3): Calcitriol is made from calcidiol, in the kidneys as well as in other organs, and is the most potent steroid hormone in the human body. Referred to as “activated vitamin D,” calcitriol is said by the experts to “unlock” a cell’s DNA library. Acting through the vitamin D receptors (VDR), calcitriol controls the expression of genes, activating about two-thirds of the ones it controls, suppressing the rest.’ Vitamin D Council
‘Once out of the lysosome (the cells’ garbage disposal system – degrades the products of ingestion & worn out organelles such as mitochondria, handles the products of receptor-mediated endocytosis such as the receptor, ligand and associated membrane) , calcidiol binds to intracellular vitamin D binding protein (IDBP) which facilitates the localization of vitamin D metabolites in the cell.’
‘The liver plays a unique role in controlling carbohydrate metabolism by maintaining glucose concentrations in a normal range over both short and long periods of times. In type 2 diabetes, alterations in hepatic glucose metabolism are observed, i.e. increased postabsorptive glucose production and impaired suppression of glucose production together with diminished glucose uptake following carbohydrate ingestion. The simultaneous overproduction of glucose and fatty acids in liver further stimulates the secretion of insulin by the pancreatic cells, and elicits further peripheral insulin resistance thereby establishing a vicious circle.’ C Postic, R Dentin, J Girard
’Low vitamin D levels and bone disease are well-recognized complications of “cholestatic” liver disease, which decreases the production or flow of bile. More recently, studies have confirmed low vitamin D levels in noncholestatic liver disease.‘ Satheesh Nair, MD, FACP
‘VDBP (vitamin D-binding protein/Gc-globulin) is converted to macrophage-activating factor by the action of either b-galactosidase from B lymphocytes or sialidase from T lymphocytes on carbohydrate side chains of the protein…VDBP-binding sites are upregulated on activated neutrophils (’plays an important role in the inflammatory response to Gram-negative bacterial infections‘), suggesting that changes in its circulating concentration might occur in inflammatory conditions. Consistent with this, in vitro work has shown that GC transcription is enhanced by proinflammatory cytokines (those which make disease worse).’ British Medical Journal
‘Recent Kidney Disease Outcomes Quality Initiative guidelines have raised concerns of 25-hydroxyvitamin D, or calcidiol, insufficiency and deficiency in patients with chronic kidney disease (CKD) not yet on dialysis therapy…a high prevalence of calcidiol deficiency and insufficiency in patients with moderate and severe CKD not on dialysis therapy regardless of geographic location.‘ Department of Medicine, Indiana University School of Medicine, Indianapolis, IN
The Lymphocytes in 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.
‘Vitamin D’s metabolic product, 1,25-dihydroxyvitamin D (calcitriol), is actually a secosteroid hormone that is the key which unlocks binding sites on the human genome. The human genome contains more than 2,700 binding sites for calcitriol; those binding sites are near genes involved in virtually every known major disease of humans’.…’The liver converts vitamin D3 (cholecalciferol) to calcidiol…those with CLD ( chronic liver disease) have reduced vitamin D blood levels because the liver’s ability to convert vitamin D3 (cholecalciferol) to circulating vitamin D (calcidiol) is reduced…risk of bone diseases such as osteoporosis which often accompanies chronic liver disease because of the liver’s reduced function.‘
3. SYNERGISTIC TOXICITY OF HEAVY METALS
The human body is bio-electric, a huge bio-conductive circuit board that runs throughout the entire body enabling all your systems to function & co-ordinate. You have 60,000 miles of blood vessels coursing throughout the body, a vast array of highways & byways & tributaries that are all inter-connected. The neurons in your brain rely on these ions to generate messages. from your brain 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 is managed via this delicate bio-conductive process. Enter Aluminum.
Aluminum is a positively charged bio-conductive element with the properties of a coagulant. It literally draws in all other metals & toxins in its path. Once injected subcutaneously into deep muscle tissue, 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, cardiac cells, breasts & ovaries in women, prostate in men, kidneys, liver & bowels.
Aluminum is the catalyst or “neighborhood bully” which coalesses all toxic debris in its path, forming a composite of sludge. Sludging loosely refers to the clumping together of all these elements bound to the coagulant Aluminum; which in turn embeds itself in the lining of your vital organs, eventually clogging the Capillaries & Arterials – the neural highways leading to the brain. These live/attenuated viruses, Thimerosal and other powerful toxins (ie. antibiotics, detergents, formaldehyde, phenol) literally piggy back in to these centers without any resistance via this bio-conductivity process coupled with the back door point of entry into the body – past the line of natural defenses. Aluminum acts as a shuttle bus which reroutes its passengers circuitously into the very epicenter of the body.
Note: Aluminum has a higher net charge than that of Thimerosal (Ethyl Mercury). Mercury is a highly corrosive element, second only to Plutonium in terms of its overall toxicity. When combined with Aluminum, Mercury forms an amalgam around this sister metal, eating through it over time. The Amalgam effect is similar to combining a powder & paste, producing a resilient binding agent.
Storehouses of bio-conductive fatty tissue (electrically charged tissue):
b. Spinal Cord/Meninges
c. Myelin Sheath
d. Breasts & Ovaries (in Women)
e. Prostate (in Men)
f. Cardiac Cells
h. Capillaries & Arterials
Currently children are getting 17 shots containing aluminum, a quadrupling of the amount given since the 1970’s. Babies weigh about 12 pounds (5.5 kg) at 2 months of age when they receive 1225 micrograms of aluminum from vaccines – 50 times higher than safety levels. Babies who follow the CDC Immunization Schedule get nearly 5000 micrograms (50 mg) of Aluminum by 18 months of age.
Note: Parkinson’s & Multiple Sclerosis are also linked to the synergistic properties of heavy metal toxicity; especially in terms of it’s effect on the Meninges/Spinal Cord, Myelin Sheath & Brain.
Major studies identifying the synergistic heavy metal toxicity factor:
a. Dr. Boyd Hayley performed a synergy experiment using Aluminum Hydroxide, Thimerosal 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. The results indicated a 75% acceleration in cell deaths when all 3 ingredients were combined.
b. “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
Aluminum + Mercury = twice the toxicity. Aluminum + Mercury + Neomycin = 3 X toxicity.
Note: 3 separate ingredients are found in multiple vaccines – each with the properties of a binding agent or coagulant.
a) Aluminum is a bio-conductive coagulant which inherently binds to any toxin
b) Ethel Mercury/Thimerosal binds with the hemoglobin (Oxygen supplier) in your red blood cells
c) Formaldehyde causes proteins to irreversibly bind to DNA
4. THE DOUBLE-EDGED SWORD – CANCER & VIRAL INFECTIONS
a. Within 72 hours of oxygen deprivation any cell will 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 the vast network of arterial veins & capillaries, inducing Ischemia.
b. Vaccine toxicity deteriorates the Glutathione levels in the body, which triggers this cascade toward Hyperthyroidism. that leads to an escalation of Free Radicals in the body – which opens to the door to heightening of acidic levels in the body. Ideally we’re supposed to be 2/3rds Alkaline – Organic Apple Cider Vinegar helps maintain optimal Alkalinity. Viruses thrive in an Alkaline deprived environment; exactly those conditions brought on by vaccine induced heavy metal toxicity. This is also triggered by bad dietary choices for these children (casein, gluten, sugars, iodized salts, polysaturated fats).
5. PREGNANCY RISKS ASSOCIATED WITH VACCINES
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; in particular during the first 6 months after birth. Essentially, mother & child share the same immunity for a minimum of 15 months; during all 3 trimesters in utero, including the entire phase whilst breast-feeding the baby after birth. 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.
While the Placenta is designed to protect the baby from outside infections, mother & baby share the SAME IMMUNITY during in utero phase. “If you vaccinate pregnant women you’re significantly elevating their immune reaction. 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 an increased risk of about 7 fold to as much as 14 fold (incidence of autism & schizophrenia in babies, and susceptible to seizures early in life or even later in life = meaning a lifetime susceptibility to chronic viral infections)…Live viruses in vaccines are incorporated into your genetic material & passed on to your children.” Dr. Russell Blaylock
Pregnant women are at a heightened risk of adverse reactions to vaccines. Thimerosal Mercury is added to the H1N1 series ostensibly to sterilize the giant multi-dose vats containing the serum. Mercury is such a fine neuro-toxin it gets absorbed into the Placenta thereby exposing the fetus, regardless of which trimester, to the potential of serious trauma & long-term side effects including asthma, allergies, chronic fatigue, autism, schizophrenia, and unfortunately in some cases, even death. ‘Flu shots are a safe way to protect the mother and her unborn child from serious illness and complications of flu. The flu shot has been given to millions of pregnant women over many years. Flu shots have not been shown to cause harm to pregnant women or their babies. It is very important for pregnant women to get the flu shot. Having a fever caused by flu infection or other infections early in pregnancy can lead to birth defects in an unborn child. Pregnant women who get a fever should treat their fever with Tylenol® (or store brand equivalent) and contact their doctor as soon as possible.’ CDC
Children have been betrayed by those “health officials” sworn (ostensibly) to protect them; who outlined a gradual phase-down plan, leading to an eventual outlawing of Thimerosal in vaccines. Mainstream Media sold the public with celebratory banner headlines. Case closed. Regrettably, behind the scenes, evidence of a “shell game” type double cross in the offing; with virtually no change in global policy on use of Thimerosal, ‘They actually did just a show removal, taking Thimerosal out of only 3.48 percent of those vaccines – and all of that was in the US, attempting to mollify, and mislead, American parents of damaged children. About 104 million childhood vaccines are administered, worldwide, each year, and only about 4 million have a preservative other than Thimerosal.’
“Injecting mercury into pregnant women and children is absurd. Examine studies which suggest otherwise, and you will find the funding for the study came from those who directly or indirectly profit from, or fear liability from, the use of mercury-containing vaccines.” Lisa K. Sykes, President of CoMeD (not-for-profit corporation that is actively engaged in legal, educational and scientific efforts to stop all use of mercury in medicine, and to ban the use of all mercury-containing medicines.
‘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.’
Placenta & Colostrum in breast milk are both vulnerable to mercury contamination from vaccines. ‘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.’ Dep’t of Health & Human Services
Hepatitis B Shot (3 doses, first given at 1 hrs old): The Hepatitis B vaccine given at birth contains 250 micrograms of aluminum. For a 6 pound baby, 11-14 mcg would be toxic. – 20 times higher than safety levels allow. Each dose also contains 50 mcgs of Thimerosal – by EPA standards a safe level for a 550 pound adult. It also contains Formaldehyde which causes Proteins to irreversibly bind to your DNA.
3,600 cases of miscarriages and stillbirths have been officially reported from 2009. 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.
Note: It is dangerous & unwise to rely on soy formula to nourish your baby through the first year after birth. Not only are you exposing your baby to genetically modified Soy product & Bisphenal A Plastic contamination (which releases a hormone similar too Estrogen leading to eventual Breast Cancer & premature sexual development); the crucial resources to be found in Colostrum are also missing.
In addition 2 separate ingredients found in some of the early vaccines are associated with infertility.
a. Neomycin / Polymixin – 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.”
VRM: The Autism Report http://vaccineresistancemovement.org/?p=10185
VRM Worldwide Autism Study
VRM: The Problem With Vaccines Part 1
VRM: The Problem With Vaccines Part 2 – Synergistic Effect of Heavy Metal Toxicity On The Body
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
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: Safe Alternatives to Vaccines
VRM: Family Charts Gradual Decline Of Daughter
VRM: Health Matters Part 1
VRM: Health Matters Part 2
VRM: Alternative Cancer Cures That Work
VRM: Pregnancy Tips
VRM: The Vanishing Sperm Count
VRM: Dr. Andrew Wakefield Being Crucified By Big Pharma
VRM: Dr. Wakefield’s Imminent Vindication – Turning Of The Tide
VRM: Media Spin & Swine Flu Hysteria
VRM: H1N1 Vaccine Surplus From 2009 Reveals Growing Distrust of Gov’t & WHO – Cost To Taxpayers Exceeds 2.5 Billion
VRM: Flu Death Statistics – WHO & The Big Lie
VRM: Canada’s 2010-11 Flu Vaccine A Deadly Concoction
VRM: United States 2010-11 Flu Vaccine Afluria – Buyer Beware
VRM: Australian Vaccine Scandal
VRM: Polio – United Nations & The Great Cull
VRM : Vaccine Industry Deception, Propaganda & Media Collusion
VRM: Birth of Medical & Scientific Dictatorship – Future Scenarios
VRM: H1N1 Bio-weaponry Incorporated
VRM : Aids & The WHO Connection – Criminal Intent
VRM: Morgellons Syndrome & Chemtrails
VRM : Council On Foreign Relations 10/16/09- Major Influence on Government Vaccine Policy
VRM: Closed Door CDC Meeting Reveals Industry Cover-up Of Heavy Metal Toxicity In Vaccines
VRM: The Rockefeller Foundation Drafts A Post-Pandemic Scenario
VRM : World Health Organization & Vaccine Manufacturers Implicated In Massive H1N1 Financial Scam Involving Kickbacks & Cover-ups
VRM : Former Pharmaceutical Representative Gwen Olsen Exposes Systemic Industry Fraud
VRM: Britain’s National Health Service – Criminal Syndicate Swindling Billions While Rapidly Destroying Health Care System
VRM: UK Institutes Brand of Medical Martial Law With ‘Super-Vaccination’ Day
VRM : The Awakening Has Begun
VRM: Medical Martial Law In The US – Sleeping Giant Of Tyranny
VRM : Multi-Virus Vaccine Quinvaxem Proving Deadly
VRM: New Generation Cancer Vaccine Will Cause Infertility
VRM: CDC-Gate Exposes A Trail of Fraud Behind Autism Studies
VRM : Squaline – The Military Agenda Comes Home
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.
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