Primary Aspects of Vaccine Toxicity Affecting the Body

Primary Aspects of Vaccine Toxicity Affecting the Body

By Joel Lord

Vaccines, by their composite nature, inherently damage & disrupt the body’s delicate neurological network; hindering the complex functioning of the brain in maintaining all systems of operation (circulatory, digestive, endocrine, immune, lymphatic, muscular, nervous, reproductive, respiratory, skeletal, and urinary). In practical terms, a synergy factor inevitably occurs when multiple ingredients such as heavy metals, live viruses/or strands of DNA-RNA “heat treated virus”, antibiotics, formaldehyde, detergent, diploid cells (aborted fetal tissue), mycoplasma, phenol dye & excipient buffers are combined together in a vial mixture.

Once these toxins are injected into deep muscle tissue or subcutaneously (either route which literally bypasses one’s natural barriers altogether), a cascading degeneration known as Ischemia, a singing of the neural pathways from toxic overload which prevents vital oxygen from reaching the brain, literally inhibiting normal development, often occurs; resulting in a series of what are termed “microvascular strokes”, ‘as large white blood cells rush to attack the foreign particles injected into our bloodstream…surround tiny capillaries where the foreign particles land, clog and collapse the capillaries.’

The viscosity of this buildup of “sludge” clogs/singes the vast network of arterial veins & capillaries leading to the brain while accumulating in the organs (ie. heart, liver, kidney), joints, meninges – 3 layers of protective tissue called the dura, arachnoid, & pia mater that surround the neuraxis (axial unpaired part of the central nervous system), intestines (gut area), along the neural pathways interlacing the entire body (resulting from “stagnant” blood). Anaphylaxis, a system-wide allergic & functional breakdown, described as ‘a severe, whole-body allergic reaction to a chemical that has become an allergen‘, and Encephalitis, inflammation of the brain & meninges (Meningoencephalitis) manifesting as ‘diffuse and/or focal neuropsychological dysfunction‘, inevitably follow.

The Myelin Sheath is a critical (electrical) insulator of the brain cells, ‘the protective sheath around axons (A long fiber of a nerve cell/neuron that acts somewhat like a fiber-optic cable carrying outgoing/efferent messages) in the nervous system…often referred to as ‘white matter’, containing a variety of fatty substances (lipids), and at least ten distinct chemicals‘; ‘formed by concentric layers of Schwann’s cell (peripheral) or oligodendrocyte (CNS) membranes  – which serves to speed up neural conduction.'‘Myelination is an essential part of human brain development. Nerves can only conduct pulses of energy efficiently if covered by myelin. Like insulation on an electric wire, the fatty coating of myelin keeps the pulses confined and maintains the integrity of the electrical signal so that it has a high signal-to-noise ratio. When the insulation on a wire is damaged or destroyed, the flow of electrical current may be interrupted and a short-circuit occurs. Oligodendrocyte cells give white matter its color by manufacturing myelin.

If myelin falls into disrepair, nerve axons cease to function, even though they themselves aren’t damaged. Protecting oligodendrocytes after brain or spinal cord injury might keep nerve cells intact. At birth, relatively few pathways have myelin insulation. Myelination in the human brain continues from before birth until at least 20 years of age. Up until the age of 10 or so, vast areas of the cortex are not yet myelinated.’

‘The way myelination takes place is through glial cells wrapping around the axons in a spiral fashion. The axons are originally embedded in these glial cells, and the cell’s membranes extend to wrap the axon tightly and repeatedly. ‘Glia’ comes from Greek, meaning ‘glue,’ hinting at the way the cell’s membrane sticks to the axon, and how the different layers of the extended membrane stick to each other. There are different glial cells that form myelin: in the central nervous system, these cells are referred to as oligodendrocytes, and in the peripheral nervous system they are Schwann cells. While in the peripheral nervous system the glial cell wraps around a single axon to insulate it, in the central nervous system a glial cell may wrap around several axons at once.’

Glycoproteins are involved in Myelin sheath formation, maintenance and degeneration: ‘Because glycoproteins are prominent components of plasma membranes, it is not surprising that they have important roles in the formation, maintenance and degeneration of myelin sheaths. The emphasis in this review is on four integral membrane glycoproteins. Two of them, protein zero (P0) and peripheral myelin protein-22 (PMP-22), are components of compact PNS myelin. The other two are preferentially localized in membranes of sheaths that are distinct from compact myelin. One is the myelin-associated glycoprotein, which is localized at the inside of sheaths where it functions in glia-axon interactions in both the PNS and CNS. The other is the myelin-oligodendrocyte glycoprotein, which is preferentially localized on the outside of CNS myelin sheaths and appears to be an important target antigen in autoimmune demyelinating diseases such as multiple sclerosis.’
http://www.ncbi.nlm.nih.gov/pubmed/12530518

“Almost any vaccination can lead to noninfectious inflammatory reaction involving the nervous system. The common denominator consists of vasculopathy that is often associated with demyelination.” Charles Posner, Harvard Medical School Department of Neurology, 1947

Two primary factors here, in determining the extent of vaccine derived neurological & corresponding neuro-developmental damage (including the host of typical auto-immune failure responses) which are often overlooked in Medical circles? Timing & synergy.

Timing is CRITICAL. A baby has no blood barrier (physiological mechanism that alters the permeability of brain capillaries so that some substances, such as certain drugs, are prevented from entering brain tissue, while other substances are allowed to enter freely) on the brain – so that vital, unfinished area is still completely raw. 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.

A baby’s  blood-brain barrier takes no less than 7 months to establish its primary protective shielding: ‘It has been established that by week 28 of the intrauterine development the process of the structural and functional establishment of the BBB (blood-brain barrier) had been over as evidenced by the lack of specific alpha-1-globulin in umbilical blood of the neonates of the given gestation age.’ Volodin NN, Chekhonin VP, Tabolin VA, Rogatkin SO, Kashparov IA.
http://www.ncbi.nlm.nih.gov/pubmed/2471140

The synergy of vaccine derived heavy metal-virus-mycoplasma-excipie​nt toxicity “sludge” targets 3 primary core “electrical grid” stations encasing the nerve center/brain – kin to throwing water over a main keyboard operating system. In the event the blood barrier, Myelin sheath & meninges are breached, particularly at such an early stage in early childhood development, neuro-developmental disorders will inevitably follow. It seems a master Electrician knows more about overall functionality of the human body than your average pediatrician.

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, 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.

This “sludging” is activated when Aluminum 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).

“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

Two excerpts from closed door meeting conducted by the CDC in 2000: “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

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.

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.

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. Dr. Christopher Shaw, Canada’s leading Neuro-Scientist released a stunning Peer Review Study in 2009 linking Aluminum in Vaccines with motor neuron degeneration found in victims of  Amyotrophic Sateral Sclerosis (ALS) & in those of Gulf War Syndrome. It followed another similar groundbreaking study begun in 2007.

‘Only mice injected with aluminum hydroxide showed significantly increased Morin labeling of cells in lumbar spinal cord compared to the other groups. Similarly, only aluminum-injected mice showed the presence of abnormal tau protein in motor neurons in lumbar cord. The multiple aluminum hydroxide injections of experiment 2 showed profound effects on motor and other behaviours. Multiple aluminum injections produced significant behavioural outcomes including changes in locomotive behaviour, and induced memory deficits on water maze tasks…We speculate that the observed neurotoxic effects of aluminum hydroxide in the present study arise by both ‘direct’ and ‘indirect’ pathways. Direct toxicity refers to the physical presence (or close proximity) of aluminum and its potential for initiating cell death pathways.’ Dr. Christopher Shaw

‘Research indicates that patients with impaired kidney function, including premature neonates, who receive injections of Aluminum greater than 4 to 5 micrograms (mcg) per kilogram of body weight per day, accumulate aluminum at levels associated with central nervous system and bone toxicity.’ Food & Drug Administration Report – 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. ‘The results for aluminum were almost identical to ethyl mercury (Thimerosal) because the amount of aluminum in vaccines goes almost exactly with the mercury.’ Dr. Tom Verstraeten/Epidemiologist

‘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.’ Study liking Macrophalgic Myofascitis to Aluminum adjuvant toxicity from vaccines

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 + 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

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% ethyl mercury 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: Original & current patent holders on 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.’

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.

‘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.’ Mercury-Autism Study 2008

‘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 & brain-stem. 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 also reveal 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.’

“The search for the association between mercury and cardiovascular disease reveals 358 scientific papers exemplifying the relationship; between mercury & cancer we find 643 scientific papers. The association of mercury with neuro-degenerative diseases is the most significant, with the references numbering 1,445. It has been shown that mercury rapidly depletes the immune system. Mercury has also been shown to induce auto-immune diseases. Anything that depletes and disturbs the immune system will increase one’s chances of contracting cancer. Mercury binds with hemoglobin, which is responsible for oxygen transport to the tissues. This results in less oxygen reaching the tissues when the body is polluted with mercury. We don’t have to look far in understanding how a heavy metal like mercury can eventually lead one to cancer’s door.” Dr. Rashid Buttar/Center for Advanced Medicine & Clinical Research
http://winningcancer.com/index.php/2010/03/heavy-metals-mercury-and-cancer/#arrive

‘Cadmium & mercury deplete selenium in the body (essential for their removal). Selenium atoms combine with cadmium & mercury atoms and escort them out of the body via the bile system. When selenium is depleted by cadmium and/or mercury, there is less selenium to form the deiodinase enzymes that convert T4 to T3, resulting in low T3 and hypothyroidism. Also there is less selenium to form glutathione peroxidase, one of the body’s prime antioxidants.’

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.’

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.’

“One nanomolar level (of Thimerosal) in the baby will prevent the macrophages from going through phagocytosis (vaccines using Thimerosal as a preservative contain a 125,000 nanomolar level of mercury). In other words, they will lose their ability to eat viruses and bacteria that are in the blood that shouldn’t be there, and so Thimerosal suppresses the immune system. This is well known and has been well described in the literature for a long time; that mercury is an immune system suppressor and you see that these autistic children have a truckload of immune problems. So you would prevent that from occurring. That is documented research and I don’t know how the government can even ignore it, or the agencies of the government can ignore it.” Dr. Boyd Hayley

‘Mercury is known to be neurotoxic and has effects on the immune system as well. Mast cells are involved in allergic reactions, and also in inflammation, and innate and acquired immunity. Autistic individuals have a 10-fold greater number of hyperactive mast cells inmost tissues. Mercury stimulates vascular endothelial growth factor and interleukin (IL)-6 release from mast cells. These mediators could disrupt the blood–brain barrier and cause brain inflammation.’ Kempuraj et al., 2010

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). Laboratory studies have found a correlation between Polysorbate 80 & ‘delayed” or stunted reproductive capacity. ‘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

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,’

Formaldehyde: Common additive in vaccines (used as “a preservative & disinfectant”, linked to cancer & chronic bronchitis) ‘can cause proteins to irreversibly bind to DNA.‘

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.’

Phenol: 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.’

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 and central nervous system effects. The toxicity of phosphates is because of their ability to sequester calcium.’

Note: Sodium Phosphate Dibasic Heptahydrate (also known as Disodium Hydrogen Phosphate) – Chemical composition includes Fluoride/50 mg/kg, Arsenic/50 mg/kg, Lead/10 ppm.‘

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. ‘It has been shown to weaken the blood-brain-barrier (BBB) and subsequently activate seizures.  It 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.‘

Sodium Borate: Ostensibly added as a “PH stabilizer” in vaccines (also known as borax). 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 stated of sodium borate (in 2005) that it is “known to be a dangerous poison, it is no longer commonly used in medical preparations.” Yet the FDA in 2006 approved the Merck vaccine ‘Gardasil’ with this “dangerous poison” to be “commonly used” in these vaccinations.

L-Histidine: 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.’…‘important for the maintenance of the myelin sheaths which protect the nerve cells.’

Note: 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 inevitably occurs 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.

Aside from all the heavy metal variants (used as adjuvants/sterilants) detergents, antibiotics, buffers, mycoplasma residue & excipients (inactive carrier/binder/filler/coating for active ingredients) commonly associated with vaccine production, the addition of live virus(es) or heat treated/modified strands of DNA/RNA (mistakenly referred to as a “killed virus”) poses serious, long-term health risks to the body. Dr. Russell Blaylock has confirmed, “Some vaccines, including the MMR, smallpox, and chickenpox vaccines, contain live viruses. By giving three and sometimes four live viruses together, the risk of developing a lifetime viral infection (a persistent viral infection) increases tremendously. This is especially so with the MMR vaccine, which contains two live viruses known to suppress the immune system for months.”

“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. Many rare forms of cancer are now very common ie Pancreatic cancer. Lymphoma is now the number one malignancy in 30 year olds and rising. Asthma has seen a ten fold increase over last 2 decades. Type 1 Diabetes has also been linked to auto-immune disorder caused by vaccines.”

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. Russell 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.’
http://www.merck.com/product/usa/pi_circulars/m/mmr_ii/mmr_ii_pi.pdf

Graphic video – live virus shedding from MMR shot given to her child spreads to mother triggering Acute Disseminated Encephalomyelitis (ADEM) & eventual Multiple Sclerosis (MS).
http://www.youtube.com/watch?v=PIXluhu4AoU

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)

Osteoporosis, Fibromyalgia (Chronic Fatigue syndrome), Macrophagic Myofasciitis, Tourette’s Syndrome, Bells Palsy, Rhematoid Arthritis, Multiple Sclerosis (MS), Acute Disseminated Encephalomyelitis (ADEM) , Lupus, Parkinson’s, ALS (Amyotrophic Lateral Sclerosis), Stevens-Johnson Syndrome, Alzheimer’s & Autism Spectrum Disorder, all manifestations of the same vaccine derived heavy metal-virus-mycoplasma-excipie​nt “sludge” breaching the body’s delicate “electrical grid” nerve center (Blood-Brain Barrier, Myelin Sheath & Meninges); literally “short-circuiting” the operation of the nervous system – ‘scarring of the myelin in the brain and spinal cord, causing varying degrees of neurological impairment…‘ ‘Physically, the brain and the spinal cord are involved. Specifically, degeneration of myelin, a material which is composed mainly of fats and serves as an insulation for the nerves, much like the covering of an electric wire, degenerates. This fatty insulation allows a nerve to transmit its impulses with lightning-like speed, enabling people to move almost without thinking. The loss of this myelin insulation causes what is, in effect, a short-circuiting so that a person loses the ability to make smooth, rapid, and coordinated movements.‘ There is a scientifically verifiable link between vaccine derived sludge-toxicity related damage to these vital areas in addition to post-vaccination ‘prescribed’ drug adverse reactions & the onset of many crippling neuro-degenerative disorders.

 

Those of us fortunate enough to have our health intact must learn from children coping with Autism. The myriad symptoms of Autism Spectrum Disorder point to a cascading breakdown in overall functionality (physiological, neurological, immunological, behavioral), the end-result of this critical premature BREACH of the “electrical grid” nerve center triggering a domino effect of systems failure throughout the body. Ultimately the gut becomes a repository for ‘pathogenic flora’, the red flag indicator associated with Inflammatory Bowel Disease, common in all Autism cases.

Symptoms of Autism Spectrum Disorder include (excerpt from VRM Worldwide Autism Study):
1. chronic rash,
2. chronic eczema,
3. Gastroenteritis,
4, floppy limbs,
5. cracking of joints,
6. chronic constipation,
7. chronic diarrhea,
8. Inflammatory Bowel Disease (Crones, Colitis),
9. Sub-Clinical Epileptic Seizures,
10. Grand Mal Epileptic Seizures,
11. Macrophagic myofascilitis,
12. Chronic Fatigue Syndrome/Fybromyalgia,
13. chronic Insomnia,
14. rolling on the back,
15. refusal to lay on stomach,
16. fanning or shaking of hands,
17. fixation on ceiling fans,
18. fixation on repetitive motions,
19. spinning in circles repeatedly,
20. tearing up paper repeatedly,
21. long stretches of silence/withdrawal,
22. complete absence of speech/verbal communication,
23. acute difficulty relating to people/objects/events,
24. indications of mental developmental delays,
25. indications of physical developmental delays,
26. serious mental & physical developmental delays,
27. prolonged difficulty using/understanding language,
28. acute sensitivity to sound/light/surroundings,
29. unusual/obsessive play with toys & other objects,
30. difficulty with changes in routine or familiar surroundings,
31. circumscribed interests are more prominent (ie. cars, trains, door knobs, hinges, meteorology, astronomy or history),
32. Attention Deficit Disorder (symptoms include inattentiveness, hyperactivity, impulsiveness, easily distracted, fidgeting, excessively talkative, physically reckless, delayed social & motor skills, plus extreme sensitivity to sensory stimuli),
33. Attention Deficit Hyperactivity Disorder (symptoms include impulsiveness, hyperactivity, inattention, fidgeting, excessive talkativeness, impatience, physically reckless, delayed social &
motor skills, plus extreme sensitivity to sensory stimuli),
34. Hypotonia (decreased muscle tone: the amount of resistance to movement in a muscle),
35. Echolalaia/Echophrasia (immediate & involuntary repetition of words/phrases spoken by others),
36. Echopraxia (the automatic repetition of movements made by another person), 37. Epstein Bar Virus (symptoms include fever, sore throat, swollen lymph glands, swollen spleen or liver),
38. Bacterial Meningitis (inflammation of thin tissue that surrounds brain & spinal cord – meninges),
39. Childhood Disintegrative Disorder (symptoms include sudden loss of motor/social/language skills, bowel & bladder control at age 2),
40. Encephalitis (symptoms include dizziness, confusion, vomiting, high fever, weakness or paralysis, impaired speech & hearing, delirium, excessive drowsiness, brain inflammation, coma),
41. Febrile Convulsions (symptoms include loss of consciousness, stiffening of body, legs/arms, jerking of head, legs & arms, skin turning pale or blue),
42. Rett’s Syndrome (symptoms include slowing of development, loss of purposeful use of the hands, distinctive hand movements, slowed brain & head growth, problems with walking, seizures & intellectual disability),
43. Mitochondrial Disorder (symptoms include muscular weakness/Hypotonia, developmental delays, epilepsy, vision & heart problems),
44. Multiple Chemical Sensitivity (acute sensitivity to commonly used chemicals products including perfumes, air fresheners & laundry softeners. The symptoms, which are chronic include fatigue and
respiratory, digestive, cardiovascular, dermatological & neurological problems)

Note: Children coping with Autism are also often prone to inward/outward directed violence; including administering self inflicted wounds, distending/biting their own tongue repeatedly, punching & breaking things, sudden jerking of the Back, lashing out at others uncontrollably. ‘They are often (if not always ) in severe pain throughout their body. Perpetual headaches, stomach aches, their skin hurts from clothing, psoriasis eczema, arthritis, bone spurs, and so on. None of which they understand. Most of which they can not explain. It is a daily, ongoing physical pain. Therefore some injure themselves in order to feel the kind of pain that they know and can understand vs the constant pain that they can not understand. This accounts for much of the headbanging, cutting themselves until they bleed and when the cut is nearly healed, they cut themselves again. Interestingly anorexics also tend to cut themselves to get out of emotional pain. ASD kids scratch their skin til they bleed, but the bleeding from scratching may feel better than the overwhelming itchiness.’ Shelley Tzorfas

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.’

The vanguard in the field of vaccine research claim “Cell-based vaccine production dramatically reduces the possibility for contamination”. No matter which route you take in terms of the application of 21st century vaccine production technology (cloning), all roads will inevitably lead to cancer. The CDC & NIAID openly admit to a “theoretical” risk of viral cross contamination, the presence of ‘endogenous retroviruses‘ (remnants of ancestral exogenous retroviral infections fixed in the germline DNA), ‘adventitious agents‘ (mutagenic viral strains) & ‘oncogenic agents’ (neoplasms or cancer), when harnessing (multiple) viruses in combination with heavy metals, tissue culture reagents, & stabilizer cocktails for vaccines. Let us review some of the noteworthy findings of National Health Regulators & Medical Practitioners/Researchers thus far: 1. ‘Because the influenza virus genome is segmented, coinfection of a single host cell with two or more different influenza viruses can result in a reassortment (or shuffle) of their genetic material.’

2. ‘Because neoplastic (cancerous) cells survive indefinitely, it is easier to qualify and bank cells that have passed all tests, especially as compared with primary cells (which are derived repeatedly from live tissue and must be re-qualified with each use).’ NOTE: Optaflu, early cell based Novartis prototype vaccine, was produced using a cell line called Madin-Darby (MDCK), cells extracted from the kidneys of a female cocker spaniel.

3. ‘Adventitious agents (mutable viruses/cross-contamination) could theoretically enter a viral vaccine through any of these ingredients ( cell substrates, vaccine seed, tissue culture reagents, stabilizers).’

4. ‘Many novel vaccines are produced in animal cell substrates, and emerging infectious diseases may theoretically be transmitted from animals to humans through these vaccines.’

5. ‘It is unclear whether neoplastic cells have a greater or lower adventitious agent risk than other types of cells. Because they can be grown for long periods in tissue culture, there may be greater opportunities for any adventitious agents to be detected.’

6. ‘If their growth in tissue culture is not well controlled, there may exist additional opportunities for contamination of cells with a longer lifespan. In cases of neoplastic cells for which the transforming event is unknown, there is also a theoretical possibility that transformation occurred as a result of a previous viral infection.’

7. ‘Because some mammalian tumors and some cells transformed by viruses contain infectious virus, cells transformed by an unknown mechanism have a theoretical risk of containing a transforming virus.’

8. ‘Over 200 viruses cause influenza and influenza-like illness which produce the same symptoms (fever, headache, aches and pains, cough and runny noses). At best, vaccines might be effective against only influenza A and B, which represent about 10% of all circulating viruses.’

9. ‘A “perplexing” Canadian study linking H1N1 to seasonal flu shots is throwing national influenza plans into disarray and testing public faith in gov’t agencies responsible for protecting the nation’s health. Study confounds infectious-disease experts in suggesting that people vaccinated against seasonal flu are twice as likely to catch swine flu.’

10. ‘There is concern that genetic technologies will be used to modify these already pathogenic agents and create “super-pathogens”. DNA shuffling (accelerated or directed molecular evolution) or combining genetic elements of distinct pathogenic viruses to create chimeric viruses, could be applied to bio-weapons enhancement.’

11. ‘Xenotropic murine leukemia (cancer) virus-related virus (XMRV) is a recently discovered human (endogenous, cloned) retrovirus that has been found in both chronic fatigue syndrome (Fibromyalgia) & prostate cancer patients. Although these findings need further confirmation, there is a potential safety concern regarding XMRV in cell substrates used in vaccines and in transmission by blood transfusion and blood products.’ FDA

Note: Consumption of genetically altered/modified organisms (GMO) is associated with infertility, excessive cancer cell growth, organ lesions, altered liver & pancreas cells, changes to enzyme levels, Immune system failure and anti-biotic resistance in animals.

“If I am able to help only one cancer sufferer to escape the excruciating and inescapable pain of death caused through treatment by ‘orthodox  methods,’ I  have  done something worthwhile.” Maurice Natenberg, author of ‘The Cancer Blackout‘

‎“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

‘No hospital admissions for gastric cancer or peptic ulcer were recorded prior to 1800 (based on inpatient records of the last two centuries from four hospitals in Scotland and three US hospitals). Hospital admissions for gastric cancer increased in an exponential fashion throughout the 19th and the beginning of the 20th century…occurrence of gastric cancer, gastric ulcer and duodenal ulcer markedly increased during the 19th century.’ A. Sonnenberg

“The war against cancer will continue to fail. Avoidable cancers will continue to become commoner and commoner and the establishment will continue to ensure that only the toxic (but highly profitable) alleged treatments of cancer which are authorized by the pharmaceutical industry will be authorized by governments. The cancer industry will not find the all powerful magic bullet cure for which it has been searching now for decades. It will fail because it is wedded to an interventionist paradigm which depends upon treating the body as a battlefield and the disease as an enemy.” Dr. Vernon Coleman

Genetics play a significant (but not central) role in determining the early onset Autism & other conditions so prevalent today. Our parents & their parents before them suffered chronic long term exposure to heavy metals & live viruses via similar mass vaccination programs given in their era. The Salk/Sabin Polio shot passed on inter-generational viruses & cancers: “Post-Polio Syndrome”, “Chronic Fatigue Syndrome”, “Myalgic Encephalomyelitis” & “Cerebral Palsy” (known as “Aseptic/Viral Meningitis”). This generational aspect of mineral depletion, which is passed on via the placenta & colostrum, strips a baby of its most vital guard during the earliest, critical stages of development. As children we inherit a varyingly compromised system based on this legacy. It’s Russian Roulette. Your immune system enters this world with a certain vulnerability.

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. The tipping point comes sooner for some than others. Further what is categorized as SIDS or Sudden Infant Death Syndrome has nothing to do with bad parenting ie. shaking your baby too aggressively. The child is in agony due to massive brain swelling. Parents who have been maligned unfairly should take courage from this knowledge.

Case in point, the HPV vaccines, Gardasil & Cervarix, contribute to “immune-mediated reactions to the nervous system” resulting in “Motor Neuron Disease” throughout the brain; and for those young teens whose threshold cannot withstand the toxic assault, due to a prolonged, compromised immune system (coupled with pre-existing medical conditions) stemming from the long-term accumulation of vaccine/anti-biotic/bad food choices inflicted erosion/saturation of the brain & gut, the eventuality of “multifocal or atypical demyelinating syndromes” (ie. Mutliple Sclerosis). Gardasil, a composite of 4 viral strains of HPV, has been linked to infertility, and a heightened risk of acquiring (an otherwise avoidable) cervical intraepithelial neoplasia grade 2, grade 3, and adenocarcinoma, and a 45% increased risk of precancerous lesions.

The Hepatitis B vaccine, typically administered to newborns in the first 12-15 hours after birth, is similarly associated with an increased risk of Multiple Sclerosis, according to a Harvard University Study ‘These findings are consistent with the hypothesis that immunization with the recombinant hepatitis B vaccine is associated with an increased risk of MS, and challenge the idea that the relation between hepatitis B vaccination and risk of MS is well understood.’.It has also been blamed for triggering Systemic Lupus Erythematosus (SLE) – which notably resulted in the eventual death of an infant, Tambra Harris, in 2009; on who’s behalf her family filed & won ‘compensation for all damages’ to the sum of $ 475,000.

The Salk & Sabin prototype of the Polio Vaccine (released in 1954), originally laced with diseased African Green Monkey Kidney Virus (SV40), has contributed to several decades of viral shedding throughout those isolated Third World communities unfortunately targeted for UN directed mass vaccination coverage – anywhere around the world, in fact, where-in the Polio vaccine program was initiated (North & South America & throughout Europe etc). ‘In recent years more than 60 scientific studies have found SV40 in rare human brain, bone and lung-related cancers, the same kinds of tumors the virus caused in laboratory animals‘. The Polio vaccine “inadvertently” spawned a host of rare or hitherto unknown forms of cancer including: Mesothelioma (fatal tumor of the membrane surrounding the lungs), Brain cancers (Primarily Ependymomas & Choroid Plexus Tumors, but also Astrocytomas, Glioblastomas, Medulloblastoma, Meningiomas), Bone cancers (Primarily Osteosarcomas, but also Chondrosarcoma & Giant Cell Tumors), Post-Polio Syndrome, Chronic Fatigue Syndrome, Myalgic Encephalomyelitis, Aseptic Meningitis & Non-Hodgkin Lymphoma. ‘Polyomavirus T antigen sequences, all of which were SV40-specific, were detected in 64 (42%) of 154 non-Hodgkin lymphomas. SV40 sequences were found most frequently in diffuse large B-cell and follicular-type lymphomas. These results add lymphomas to the types of human cancers associated with SV40.’

The trivalent influenza vaccine contains 3 sets of either ‘killed’ or ‘heat-treated DNA/RNA strands, ostensibly a safe variant blueprint of the live virus itself. Adjuvants are designed to jump-start or supercharge the immune system – to induce a robust immune response; thus immunizing the body against the likelihood of succumbing to the flu while avoiding the direct spread of infection. In truth no virus is fully killed during the vaccine manufacturing process. Typically the vaccinee is left more susceptible to catching the seasonal flu (twice a likely to catch swine flu). Depending on the degree of compromised immune system &/or pre-existing medical condition involved, a vaccine induced Cytokine Storm can rapidly trigger complete auto-immune failure throughout the individual’s body.

‘A cytokine storm is the systemic expression of a healthy and vigorous immune system resulting in the release of more than 150 inflammatory mediators (cytokines, oxygen free radicals, and coagulation factors). Both pro-inflammatory cytokines (such as Tumor Necrosis Factor-alpha, InterLeukin-1 & InterLeukin-6) and anti-inflammatory cytokines (such as interleukin 10, and interleukin 1 receptor antagonist) are elevated in the serum, and the fierce and often lethal interplay of these cytokines is referred to as a “Cytokine Storm”.

The primary contributors to the cytokine storm are TNF-a (Tumor Necrosis Factor-alpha) and IL-6 (Interleukin-6). The cytokine storm is an inappropriate (exaggerated) immune response that is caused by rapidly proliferating and highly activated T-cells or natural killer (NK) cells. These cells are themselves activated by infected macrophages. The cytokine storm must be treated and suppressed or lethality can result.’
http://www.cytokinestorm.com/

Manifestations of a vaccine triggered Cytokine Storm can range from high fever & extreme vomiting to Bronchitis, Hemorrhagic fever (drowning of lungs with fluid), Anaphylaxis (severe allergic reaction), Guillain–Barré syndrome (form of paralysis), Encephalitis (brain inflammation), Acute Respiratory Distress Syndrome, Sepsis (overwhelming immune response/inflammation/organ failure linked to bacterial infection), Bacterial Pneumonia, Febrile Convulsions, Sub-Clinical Epileptic Seizures, Grand Mal Epileptic Seizures, Narcolepsy, organ failure, blindness, coma & death. ‘A family is in mourning (Australia/2010) after their toddler unexpectedly died less than 12 hours after receiving a seasonal flu vaccination…National health authorities have ordered doctors to stop giving seasonal influenza vaccinations to children under five after dozens of serious reactions, including convulsions.’

Prevnor, 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. “Available data suggest that PCV7 (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.”.

There is yet another unseen danger, altogether ignored in mainstream medical circles, the buried track-record of post-vaccine adverse drug reactions. Over-the-counter painkillers typically exacerbate Vaccine injuries. Tylenol ‘uses up glutathione (GSH) stores and metabolites of acetaminophen accumulates causing direct damage to liver cells‘, weakening the gut & crucial mitochondrial integrity; while anti-inflammatory drugs (aspirin & ibuprofen) associated with ‘stomach aches, indigestion & ulcers which can eventually lead to GI bleeding or may even perforate, spilling the contents of the stomach or small intestine into the sterile abdominal cavity‘.

Prescription drugs are particularly carcinogenic on the body, in terms of their synergistic effect, when combined with vaccine related toxic debris. Gardasil, for instance, is known to trigger “multifocal or atypical demyelinating syndromes” (aka Multiple Sclerosis). The Medical Industry promptly recommends MS treatment therapy (Copaxone) for those who develop MS-like symptoms after receiving the Gardasil regime. Contrary to all the Industry fanfare praising the drug, it turns out Copaxone adverse effects ranging from Respiratory Arrest, Tremors, Cardiovascular Disorder, Suicidal Ideation, Shock, Cardiac Disorder Thrombosis, Renal Disorder & Multiple Sclerosis (58 Cases of Multiple Sclerosis Relapse) to numerous incidents of deaths were deliberately buried from Press Publications; while references to negative test results in mice from early Clinical Trials were also conveniently omitted.

‘Israeli generics giant Teva Pharmaceutical Industries is suffering a couple of Copaxone-related headaches. First, Israel’s health ministry appointed a special committee to probe a trial of the MS drug. Allegedly, Teva tested Copaxone on ALS patients–despite the fact that previous trials on mice had failed. Teva maintains that testing Copaxone in human ALS patients was perfectly safe despite the deaths seen in mice taking the drug, because Copaxone had already made it through plenty of human trials for its approval as an MS drug. But an internal investigation by the health ministry’s comptroller found that the company didn’t submit all the necessary info before trial approval. So the special committee will take a look at the evidence to see whether the ministry and/or the company did anything wrong.’

Another horror, anti-psychotic drugs, typically prescribed to children with “severe” Autism, trigger what is termed ‘Tardive dyskinesia‘ – characterized by ‘repetitive, involuntary, purposeless movements. Features of the disorder may include grimacing, tongue protrusion, lip smacking, puckering & pursing, rapid eye blinking. Rapid movements of the arms, legs, trunk may also occur.’ This is kin to throwing petrol on a wild-fire. The similarities between these drug “side-effects” and behavioral aspects of classic Autism long documented in the field, beg serious questions to be answered. Are children being pushed over the edge, their conditions made worse (or brought on) by drugs inadvertently designed to inflame the symptoms? In fact the Mayo Clinic openly endorses the use of drug therapy for treatment of Autism symptoms, ‘No medication can improve the core signs of autism, but certain medications can help control symptoms. Antidepressants may be prescribed for anxiety, for example, and antipsychotic drugs are sometimes used to treat severe behavioral problems.’

A family in the UK recently lost their baby boy, “22 months at death”, following post vaccination adverse drug interactions. Up until that point their baby had received the full slate of injections typical for his age group. At 6 months he began to experience ongoing convulsions/seizures. His neurologist then chose to prescribe him a set of experimental drugs (none of which are officially licensed for use in infants): ‘Sodium Valproate’ or ‘Valproic Acid’ (anti-convulsant, anti-psychotic – anti-seizure medication), ‘Keppra’ or ‘Levetiracetam’ (anti-epileptic drug) & ‘Clobazam’ (benzodiazepine type anti-convulsant) – ostensibly to quell his seizures. Initially he was put on a combination of Sodium Valproate & Keppra. A decision was then made to switch Keppra for Clobazam, as, per the neurologist in charge, “It was clearly making him worse.” There was speculation of possible Dravet’s Syndrome (severe myoclonic epilepsy in infancy). At no time during this phase were the parents ever consulted or briefed on the authorization of these drug combinations given to their child.

There is ample scientific literature pointing to an escalation of symptoms once specific drugs are combined. The father subsequently learned, “Clobazam makes the Sodium valproate over react by something like 70%”. Further, ‘When clobazam is added to a therapy regimen that includes valproic acid, the patient should be closely followed for possible adverse drug reactions caused by elevated valproic acid serum concentrations, and monitoring of valproate serum levels should be considered‘…’Valproic acid may cause serious or life threatening damage to the liver…greatest in children who are younger than 2 years of age and in people who are taking more than one medication to prevent seizures…any condition that affects the ability to think, learn, and understand.’

The parents, now estranged, marked the date of what would have been their child’s 2nd birthday in solemn remembrance of their son; born August 4, 2009, died June 21, 2011. The father duly noted “Each time he was given shots he seemed to have seizures…overdose symptoms were heart block, coma, death.” Max, may you rest in peace.

Note: One way fair justice will be served in this instance is directly through the courts. Whether this child died prematurely due to gross incompetence or well-meaning ignorance, a financial settlement will be reached at some point. However one glaring factor remains that we must consider – a family put their trust in an Industry sworn to protect the innocent. And yet they were not briefed on the synergistic nature of anti-seizure medications when combined. Nor were they prepared for the seizures which suddenly gripped their child at 6 months, the result of vaccine induced Encephalitis; inflammation of the brain & meninges (Meningoencephalitis) manifesting as ‘diffuse and/or focal neuropsychological dysfunction‘.

Whose responsibility was this? Certainly most parents aren’t versed in the hard science & reasoning behind vaccine methodology. Who can blame them, given these hurried modern times? But if that is the case, then isn’t it the obligation of doctors making these pivotal life-changing decisions to have all the facts straight beforehand? This child is unfortunately gone. But the message still resonates and his legacy will hopefully serve as a burning light of truth for parents throughout our communities, that it is now time to step back and rethink the entire concept of “herd immunity”.

How is it that so many parents traditionally adhere to standard vaccine protocols for their children, given the shoddy track record of virtually every vaccine program ever instituted in the field? The old adage “Out of sight, out of mind” has a dual meaning in these tyrannical times, “Out of mind, out of sight.” Most can’t PERCEIVE anything out of the ordinary, primarily because their “programing” has been designed through mass societal ’social engineering”, to look past the obvious; trusting implicitly, these high priests of modern medicine, draped in white frocks, delegated to maintain (contain) “the herd”. This is our greatest obstacle – ingrained societal blindness to Gov’t directed tyranny. In the case of National Health directives visa vi vaccine uptake, the evidence overwhelmingly supports caution at the very least; given the litany of conflicts of interest stacking the deck throughout the World Health Organization, CDC, FDA. Vaccine Lobby, Mainstream Media outlets, & Local/Federal Gov’t administered Health Dep’ts.

 

The public has a right to know all the pros & cons of subscribing to the Vaccine Industry. After all we are the target market. It is particularly incumbent upon us as parents to know all the risks involved before exposing our children to potential harm. And yet, given our sheer strength of numbers & moral responsibility of purpose, the vast majority, historically, will defer that power to Gov’t institutions & fraudulent UN mandates without conducting any formal research on the subject; overlooking their natural born, inherent rights to self-determination of the body.

That is why we MUST be the generation which turns the tide. Our children are counting on us to steer the course toward a brighter & healthier future. It is up to you.

Article continued via VRM: The Problem With Vaccines Part 5A – Detoxification & Restoration of Body

See: VRM: The Problem With Vaccines

See: VRM: The Problem With Vaccines Part 2 – Synergistic Effect of Heavy Metal Toxicity On The Body

See: VRM: The Problem With Vaccines Part 3 – Synthetic Genomics & The Death Of Natural Immunity

See: VRM: Vaccine Clinic – Concise Compendium To The Problem With Vaccines

See: VRM: Worldwide Autism Study

See: VRM: “One For All” Universal Flu Vaccine – 21st Century Genetic Roulette Part 1

See: VRM: “One For All” Universal Flu Vaccine – 21st Century Genetic Roulette Part 2

See: VRM: Gardasil/Cervarix – A Legacy Of Shame

See: VRM: Gardasil/Cervarix Part 2 – Demyelination, Multiple Sclerosis & the Copaxone Connection

See: VRM: Dr. Andrew Wakefield Being Crucified By Big Pharma

See: VRM: Dr. Wakefield’s Imminent Vindication – Turning Of The Tide

See: VRM: Family Charts The Gradual Decline Of Daughter Attributed To Vaccine Trauma

See: VRM: Australian Vaccine Scandal

The Vaccine Resistance Movement has always been a non-profit organization; therefore your financial support is integral to us reaching our many ambitious goals. If you appreciate the efforts to bring this information forward do consider making a donation. Any amount, no matter how modest, will help us raise the stakes to better counter an increasingly dictatorial pro-vaccine lobby & corrupt Gov’t bureaucracy bent on eliminating the link between vaccines & Autism. Your support will help us expand our horizons, enabling us to reach a much broader community around the world, with many projects currently on the go (aside from helping us cover the basic costs involved in maintaining day-to-day operations, rally costs, speaking engagements etc); while making it possible for us to bring our VRM Worldwide Autism Study to the world stage. Please see Paypal link on the VRM website. thx.

 From http://vaccineresistancemovement.org/?p=8787

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