List of Vaccine Fillers: Officially administered by design with vaccines provided to the public; in addition to the viral & bacterial RNA or DNA (combinations of excipients vary depending on specific vaccine series) –
Recycled animal tissues: variants of pig blood, horse blood, rabbit brain, dog kidney, a continuous line of monkey kidney cells, washed sheep red blood cells, chick embryo, chicken egg, duck egg, calf (bovine) serum beta-propiolactone, fetal bovine serum, Porcine (pig) pancreatic hydrolysate of casein, Vero cells
Human diploid cells/Residual MRC5 proteins (originating from human aborted fetal tissue)
Monosodium glutamate (MSG)
Phenol red indicator
VRM analysis of vaccine fillers:
ALUMINUM (two variants) – directly linked to Alzheimer’s Disease and suspected in Macrophagic Myofasciitis & Chronic Fatigue Syndrome. 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), MMR, Hib, Pneumococcal & Gardasil (HPV) vaccines. 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.
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), MMR, Hib, 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.‘
AMMONIUM SULFATE – an inorganic chemical compound used a fertilizer and “protein purifier”; known to cause kidney & liver damage, gastrointestinal disfunctions
AMPHOTERICIN B – an “antifungal disinfectant”, damages the urinary tract, bowels, heart functions
BETA-PROPIOPACTONE – ranked as one of the most hazardous compounds (worst 10%) to humans and “reasonably expected to be a human carcinogen” (International Agency for Research on Cancer – IARC, 1999).
EGG PROTEINS – includes Avian Viruses.
FORMALDEHYDE – used as “a preservative & disinfectant”, can cause proteins to irreversibly bind to DNA, known to cause cancer, chronic bronchitis, eye irritation when exposed to the body’s immune system.
L-HISTIDINE (0.78 mg of L-histidine) – L-Histidine is a diet related ‘essential amino acid‘, also responsible for forming metal bearing enzymes (ie.metallothionein), a precursor to the allergy symptom producing hormone histamine; a synthetic form of which is added exclusively to Gardasil. ‘L-histidine supplements carry warnings that such supplements should be avoided by children, pregnant women, and nursing mothers.‘. Chemical composition: Chloride – 16.66-17.08%, Ammonium – ≤0.02% Heavy Metals (as Pb) – ≤10ppm Arsenic – ≤1ppm.
‘L-histidine can pass through the placental wall to the fetus. This could be the direct cause to the spontaneous miscarriage and birth defects in some of the babies. MSDS (material safety data sheet) Section 11: Toxicological Information, Special Remarks on Chronic Effects on Humans: ‘Passes through the placental barrier in humans.’
‘In the histamine-treated sample, thrombin (blood clotting) production increased more than 5-fold from the baseline value after 30 min. After the initial time point, significantly more thrombin was formed in the histamine-activated samples.’
‘L-histidine is important for the maintenance of the myelin sheaths which protect the nerve cells. It is also needed for the production of both red and white blood cells. L-Histidine also protects the body from radiation damage, helps to lower blood pressure, and aids in removing heavy metals from the system. Histamine, an important immune system chemical, is derived from histidine.’
Whenever a vital, naturally occurring substance such as L-histidine is injected into the body subcutaneously (alongside heavy metals, live/attenuated viruses, detergents & antibiotic excipients etc) the end result, a counter effect inevitablyoccurs where-in the immune system cannot differentiate between the naturally occurring amino acid in the body from that present in the vaccine; registering all these intruders as a common enemy of toxic debris. The immune system instinctively kicks into overdrive, alerting any available antibodies throughout the body to identify & eliminate deposits of L-histidine it encounters in its path.
The end result, in each case, we’re seeing the antithesis of nature’s course develop, as the body, stripped of one or more primary components, is now, in essence, at war with itself. What follows is cascade of unfortunate auto-immune reactions; neurological & neuro-developmental breakdown.
MSG (Monosodium Glutamate) – Now known to cause cancer in humans, also linked to obesity
NEOMYCIN & POLYMYXIN – 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.
PHENOL – a highly toxic disinfectant dye, attributed to liver, kidney, heart & respiratory damage. ‘Phenol is so deadly that is was used by the Nazis as a means of extermination during the World War II. Phenol injections were given to thousands of people in concentration camps – especially at Auschwitz-Birkenau – to kill those who were mentally ill, had incurable tuberculosis and were permanently incapable of work.’
PHENOXYETHANOL (ANTIFREEZE) – proven to have extreme neurotoxic side effects.
POLYSORBATE 80 (also referred to as 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 follicles.
‘Neonatal female rats were injected ip (0.1 ml/rat) with Tween 80 in 1, 5 or 10% aqueous solution on days 4-7 after birth. Treatment with Tween 80 accelerated maturation, prolonged the oestrus cycle, and induced persistent vaginal oestrus. The relative weight of the uterus and ovaries was decreased relative to the untreated controls. Squamous cell metaplasia of the epithelial lining of the uterus and cytological changes in the uterus were indicative of chronic oestrogenic stimulation. Ovaries were without corpora lutea, and had degenerative follicles.
“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
POTASSIUM CHLORIDE – Used as part of a phosphate buffered saline in the shot. The majority of the potassium chloride produced is used for making fertilizer, since the growth of many plants is limited by their potassium intake. As a chemical feedstock it is used for the manufacture of potassium hydroxide and potassium metal; and as a flux for the gas welding of aluminium. Hyperkalemia. May induce Cardiac arrest (especially in renal impairment or if administered too rapidly). May cause pain and thrombophlebitis if administered in high concentration into small veins in patients with cardiac disease, renal impairment, or acidosis: monitoring of acid-base balance, potassium levels, and ECG is recommended. Potassium chloride is also used as the third of a three-drug combination in lethal injection. Additionally, KCl (AN aqueous solution form of Potassium Chloride) is used, albeit rarely, in fetal intracardiac injections in second- and third-trimester induced abortions.
SODIUM PHOSPHATE DIBASIC HEPTAHYDRATE & POTASSIUM PHOSPHATE MONOBASIC: Both excipients (pharmacologically inactive substances, carriers for the active ingredients of a medication) used as part of a phosphate buffered saline in the shot. May sequester calcium and cause calcium phosphate deposits in kidneys. Chronic ingestion or inhalation may induce systemic phosphorous poisoning. Liver damage, kidney damage, jaw/tooth abnormalities, blood disorders & cardiovascular effects can result. Phosphates are slowly and incompletely absorbed when ingested, and seldom result in systemic effects. Such effects, however, have occurred. Symptoms may include vomiting, lethargy, diarrhea, blood chemistry effects, heart disturbances, nausea, vomiting, stomach/abdominal pain or bloating, dizziness, or headache andcentral nervous system effects. The toxicity of phosphates is because of their ability to sequester calcium.
SODIUM DEOXYCHOLATE – A detergent added to new generation of ‘Split Vaccines’ to modify the whole virus which causes cell death and symptoms such as burning, redness, and swelling. ‘Vanderbilt University School of Medicine researchers showed that the pharmacokinetics and toxicity of sodium deoxycholate produced an inflammatory response that persisted 10 days. Deoxcyholate also induces DNA damage and apoptosis in human colon. Because secondary bile acids are thought to be genotoxic, exposing colon epithelial cells to secondary bile acids may induce DNA damage that might lead to apoptosis.‘ It has been shown to weaken the blood-brain-barrier (BBB) and subsequently activate seizures. It also demonstrates synergistic toxicity — notably with Amphotericin B, the antifungal listed above. Recommended for stripping endotoxin (Lipopolysaccharide or LPS) from immobilized Polymyxin B columns; for use with the the Thermo Scientific Detoxi-Gel Endotoxin Removing Gel. ‘The effectiveness of a detergent in any application is dependent on the detergents concentration. Too much or too little detergent can often have a deleterious effect.‘
RE-CYCLED ANIMAL TISSUE (multiple) – the building blocks of Mad Cow Disease
RESIN AND GELATIN – known to cause allergic reaction
SODIUM BORATE (35 mcg of sodium borate) – Sodium borate, also known as borax, is ostensibly added as a “PH stabilizer” in vaccines. It is also a recognized toxic substance used in roach, rodent, and insect killers, antiseptics, some paints and enamels.
‘The National Library of Medicine (NLM) of the National Institutes of Health notes of sodium borate that it “is now known to be a dangerous poison, it is no longer commonly used in medical preparations.” That was published in 2005. Yet the FDA in 2006 approved the Merck vaccine with this “dangerous poison” to be “commonly used” in these vaccinations. The symptoms of sodium borate poisoning according to the NLM citation include many of the side effects being reported after less than six months of the vaccine usage. These include convulsions, collapse, and seizures that include twitching of facial muscles, arms, hands, legs, and feet.’
TRITON X100 – detergent, added to new generation of ‘Split Vaccines’ to modify the whole virus
THIMEROSAL (MERCURY) – a neurotoxin linked to psychological, neurological & immunological problems. Nervous system damage, kidney disease, birth defects, dental problems, mood swings, mental changes, hallucinations, memory loss, nerve damage and inability to concentrate can occur. Symptoms also include tremors, loss of dermal sensitivity, slurred speech and, in rare cases, even death and paralysis. This additive alone was the catalyst for another recent Class Action Lawsuit organized by mothers of children born with Autism & the many related behavioral disorders associated with it. Autism is now occurring at levels never seen before in history, 1 in 67. The average used to be 1 in 20,000. Thimerosal Mercury is added to vaccines ostensibly to sterilize the giant multi-dose vats containing the serum.
MERCURY-AUTISM STUDY 2008: Emerging evidence supports the theory that some autism spectrum disorders (ASDs) may result from a combination of genetic/biochemical susceptibility, specifically a reduced ability to excrete mercury (Hg), and exposure to Hg at critical developmental periods. Elemental/inorganic Hg is released into the air/water where it becomes methylated and accumulates in animal tissues. The overwhelming preponderance of the evidence favours acceptance that Hg exposure is capable of causing some ASDs.
Studies have shown that mercury is taken up in the periphery by all nerve endings and rapidly transported inside the axon of the nerves (axonal transport) to the spinal cord & brainstem. Unless actively removed, mercury has an extremely long half-life of somewhere between 15 and 30 years in the central nervous system. Hair analysis showed mercury levels to be 20,000 higher in those with cardiac abnormalities.
Studies have shown that the level of mercury in the umbilical cord blood of newborns is 1.7 times higher than the mercury level in their mother’s blood. Eating fish just two or more times a week has been found to raise mercury levels seven times beyond those in women who had not eaten any fish for a month, according to the CDC. While Thimerosal Mercury contained in vaccines gets absorbed into the Placenta interfering with early development.
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 & the Gastro-Intestinal Tract or the guts. 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).
The viscosity of this toxic sludge resulting from vaccines which accumulates in the organs (ie. heart, liver, kidney), 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.
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.’
“Cancer was practically unknown until compulsory vaccination with cowpox vaccine began to be introduced. I have had to deal with at least two hundred cases of cancer, and I never saw a case of cancer in an unvaccinated person.”Dr. W.B. Clark of Indiana/1936
‘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
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
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.’
Vaccine related injuries: Short list of Auto-Immune Diseases
1) Chronic Fatigue Immune Disfunction
4) Multiple Sclerosis
5) Arterial Sclerosis (Lou Gehrig’s Disease)
6) Rhematoid Arthritis
7) Adult & Juvenal Type 1 Diabetes
8) Crohn’s Disease
9) Guillaine-Barre Syndrome
10) Bells Palsy
11) Stevens-Johnson Syndrome
Vaccine related injuries: Childhood afflictions include –
1) Chronic Draining Ear Infections
2) 600% increase In Autism
6) Chronic Allergies
Vaccine related injuries: Cancers include –
4) Aids Complex
5) Gulf War Syndrome
Note: These Cancer Epidemics were never seen before or very rarely before 50-60 years ago