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.’ National Institute of Neurological Disorders & Stroke

‘Ischemia is known to lead to hyperexcitability of neural tissue.’ Charles A. Lantz, Ph.D. on the impact of Ischemia & resulting vertebral subluxation (misalignment of spinal bones) on neural function

“Almost any vaccination can lead to noninfectious inflammatory reaction involving the nervous system. The common denominator consists of vasculopathy (disease of the blood vessels) that is often associated with demyelination (permeation of the critical “electrical” insulator of the brain cells).” Charles M. Poser, Harvard Medical School Department of Neurology, 1947

‘Approximately 25% of the total amount of the cholesterol present in humans is localized to this organ, most of it present in myelin. Almost all brain cholesterol is a product of local synthesis, with the blood-brain barrier efficiently protecting it from exchange with lipoprotein cholesterol in the circulation.

It has been estimated that up to 70% of the brain cholesterol is associated with myelin. Because up to half of the white matter may be composed of myelin, it is unsurprising that the brain is the most cholesterol-rich organ in the body. The concentration of cholesterol in the brain, and particularly in myelin, is consistent with an essential function related to its membrane properties.‘ Division of Clinical Chemistry, Huddinge University Hospital, Sweden

‘In a model of aluminum-mediated intoxication imposed to mice during pregnancy and early development, a 72% higher content of lipid peroxidation products was found in brain myelin.’ Department of Biological Chemistry, University of Buenos Aires, Argentina, 08/15/1997

Note: Lipid peroxidation is associated with cellular damage resulting from oxidative stress (or Ischemia), which inhibits the capacity of cellular antioxidants, vital to natural immunity, by the unleashing of free radicals. – Scientific verification of demyelination linked to mitochondrial breakdown, caused by the intervention of aluminum on early childhood development in the brain.

‘Aluminum is now being implicated as interfering with a variety of cellular and metabolic processes in the nervous system and in other tissues.‘ Aluminum Toxicity in Infants and Children (RE9607), Pediatrics Volume 97, Number 3 March, 1996, pp. 413-416

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.

‘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.

The Myelin Sheath is also significantly under-developed at birth. In fact, a baby undergoes continuous Myelin formation well after birth.

‘Myelination appeared to occur earliest in the posterior fossa, with the middle cerebellar peduncle identifiable at only 3 months. By the age of 1 year, all major white matter tracts including the corpus callosum, subcortical white matter, and the internal capsule were well defined. However, due to subtle changes in appearance, the refined configuration of the adult brain was not attained until early adolescence.‘ B A Holland, D K Haas, D Norman, M Brant-Zawadzki and T H Newton

Similarly, the Meninges layering is designed to insulate the brain & spinal cord from injury – notwithstanding the accumulative barrage of synergistic toxicity associated with early childhood vaccines. “Probably no field in embryology has been less explored than that relating to the meninges.” Lewis H. Weed

There is no safe threshold for vaccines whatsoever.

‘The organs of the central nervous system (brain and spinal cord) are covered by 3 connective tissue layers collectively called the meninges. Consisting of the pia mater (closest to the CNS structures), the arachnoid and the dura mater (farthest from the CNS), the meninges also support blood vessels and contain cerebrospinal fluid. These are the structures involved in meningitis, an inflammation of the meninges, which, if severe, may become encephalitis, an inflammation of the brain.’ Medline Plus

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.

The synergy of vaccine derived heavy metal-virus-mycoplasma-excipient 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-Brain barrier, Myelin sheath & Meninges are breached, particularly at such a critical 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), Hib, Pneumococcal & Gardasil (HPV) vaccines. Based on Dr. David Ayoub’s findings children, on average, receive 2-400 micrograms per vaccine, almost half 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

Dr. Boyd E. Hayley performed a synergy experiment using aluminum hydroxide, mercury & neomycin (antibiotic associated with Kidney Failure, hazardous to a fetus):

A set of 100 healthy cells were exposed to Aluminum. All the cells died at a certain rate. Another batch of healthy cells were then exposed to Thimerosal Mercury. All the cells died at a comparable rate.  A third test of this kind was conducted using Neomycin. All the cells died at a similar rate. Then Haley exposed a healthy set of cells to Aluminum & Thimerosal together. The cells died at twice the previous rate. Finally he combined Aluminum, Thimerosal & Neomycin under the same conditions.

Note: The results indicated a 75% acceleration in cell deaths when all 3 ingredients were combined.

Thimerosal Mercury in vaccines permanently damages tissue sensitivity –  ‘Neonatal administration of a vaccine preservative, thimerosal, produces lasting impairment of nociception (awareness of tissue injury) and apparent activation of opioid system in rats. Present findings show that THIM (Thimerosal) administration to suckling or adult rats impairs sensitivity to pain, apparently due to activation the endogenous opioid system.’

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-invigorated 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

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.’

Mother & child share the same immunity while the baby is ‘In Utero’ (all 3 trimesters) & for the entire duration of breast-feeding after birth. 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 goes without saying that pregnant women are at a heightened risk of adverse reactions to vaccines.

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 Institute of Chronic Illnesses, Inc., CoMeD, Inc., and The Genetic Centers of America, Silver Spring, Maryland, USA

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.

Pregnant patients whose provider recommended and offered influenza vaccination were almost 5 times more likely to be vaccinated for influenza than patients who reported that their provider did not make a recommendation or offer influenza vaccination…Please encourage your pregnant and postpartum patients to get vaccinated against Influenza.’  Heim LJ, Nichols KJ, Palfrey JS, et al; US Department of Health & Human Services. Dear Colleague letter on vaccination in pregnant and postpartum women., 09/15, 2010 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

Note: It is imperative that pregnant women avoid ALL Mainstream over-the-counter & Prescription painkillers, sedatives, antibiotics, anti-viral//bacterial-type medication, antihistamines, antiperspirants; including the entire regime of vaccines (particularly the Flu shot). Your baby must be your first priority.

Prenatal paracetamol (aka Tylenol) exposure and child neurodevelopment: ‘The sibling-control analysis revealed that children exposed to prenatal paracetamol for more than 28 days had poorer gross motor development, communication, externalizing behaviour, internalizing behaviour, and higher activity levels. Children exposed to long-term use of paracetamol during pregnancy had substantially adverse developmental outcomes at 3 years of age.‘ Brandlistuen RE, Ystrom E, Nulman I, Koren G, Nordeng H.

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 (added to the Gardasil series) 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.’

Graphic video – live virus shedding from MMR shot given to her child spreads to mother triggering Acute Disseminated Encephalomyelitis (ADEM) & eventual Multiple Sclerosis (MS).

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, RhematoidArthritis, 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-excipient “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.

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

See VRM: The Autism Report