‘Minor illnesses such as upper respiratory infection with or without low-grade fever are not contraindications for use of ActHIB vaccine. As reported with Haemophilus b polysaccharide vaccines, cases of H influenzae type b disease may occur subsequent to vaccination and prior to the onset of protective effects of the vaccine.’
http://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/ApprovedProducts/ucm109841.pdf

‘Although Hib vaccines may not directly cause Hib disease, individuals exposed to Hib disease could more easily develop serious Hib illness soon after Hib vaccination. In 1987 the US introduced a more effective Hib vaccine, diphtheria conjugated vaccine (PRP-D), which was suitable for 18 month and older children. It was this vaccine that Australia licensed in 1992, also for 18 month and older children. Did this vaccine also carry an increased risk of early-onset Hib disease? The possible increased risk of Hib disease soon after Hib vaccination prompted immunological studies into several Hib vaccines. Animals more easily developed meningitis soon after Hib vaccination. 18 month old children with natural Hib antibody experienced a fall in antibody two days after vaccination before protection developed. The studies indicated that PRP-D was the most potent vaccine, but this vaccine produced most early-onset meningitis and most bacteraemia and the biggest fall in natural antibody at day two. The most effective vaccine appeared to involve the greatest risk.

The concentration of serum Hib antibody needed for protection is believed to be at least 0.15 but possibly 1.0 micro-grams per millilitre. In 18 month old children PRP-D vaccination caused natural Hib antibody to fall typically from 0.18 to 0.04 micrograms per millilitre at day two before rising to 7.20 micrograms permillilitre at day seven.’
http://www.whale.to/vaccines/hib1.html

On December 13, 2007, certain lots of Haemophilus influenzae type b (Hib) vaccine marketed as PedvaxHIB (monovalent Hib vaccine) and Comvax (Hib-HepB vaccine), and manufactured by Merck & Co., Inc., were recalled voluntarily, and the company temporarily suspended production of these vaccines. “This child eventually died from contracting Meningitis.”
http://www.cdc.gov/mmwr/preview/mmwrhtml/mm5824a5.htm?s_cid=mm5824a15e

3. Meningitis type C Vaccine

Meningitec manufactured by Wyeth – Meningococcal Group C Conjugate Vaccine. Active ingredients: Each vial contains 10 micrograms meningococcal Group C oligosaccharide conjugated to 15 micrograms of diphtheria CRM197 protein. Other ingredients: Aluminium phosphate, Sodium chloride, Water for injections.
Serious Effects: If any of the following happen, tell your doctor or pharmacist immediately or go to Accident and Emergency at your nearest hospital: Sudden signs of allergy such as rash, itching or hives on the skin, swelling of the face, lips, tongue or other parts of the body, red or purple flat pinhead spots or bruising appear under the skin, shortness of breath, wheezing or trouble breathing, chest pain, temporarily stopping breathing, a seizure (fit) or convulsion, which may be accompanied by a very high temperature, feeling weak or paralysed, or generally feeling sore or tender, dark coloured urine or pale stools, relapse of a kidney condition called nephrotic syndrome. These are very serious side effects that may need urgent medical attention.
http://www.novaccine.com/pdffiles/Meningitec_package_insert.pdf

NOTE: Hazards include meningococcal Group C oligosaccharide (strands of attenuated DNA/RNA derived from a live virus), Aluminium phosphate (highly conductive heavy metal adjuvant or booster linked to Ischemia & a host of neuro-degenerative disorders including Alzheimer’s Disease).

‘A series of government documents obtained by The Observer, a British newspaper, has revealed that more than 16,000 adverse reactions possibly linked to two vaccines have been reported in the past 10 months, including 12 deaths that occurred in people after being vaccinated. The vaccines in question, Meningitec and Meninjugate, are designed to offer protection from meningitis C, which strikes approximately 1,500 people in the United Kingdom every year.’
http://www.vaccineinfo.net/immunization/vaccine/meningococcal/under_scrutiny.shtml

‘Four of the medical experts advising the Government on whether the new meningitis C vaccine is safe have links to one or more of the drug companies that produce it, The Observer has discovered. The Department of Health last night confirmed that Professor Janet Darbyshire, a member of the Government’s Committee on Safety of Medicines, had received support for academic research from US firms Wyeth and Chiron, who produce the two main meningitis products being used on children in Britain: Meningitec and Meninjugate. Darbyshire is professor of epidemiology at London University and director of the Medical Research Council. ‘
http://www.guardian.co.uk/uk/2000/sep/03/tracymcveigh.martinbright

“Epidemics of aseptic meningitis due to enteroviruses following national immunization days in Bahrain” (Annals of Tropical Paediatrics, vol. 18, no. 2, June 1998, pp. 101-9): Two successive epidemics of aseptic meningitis due to enteroviruses were observed after national immunization days against polio, comprising 286 and 169 cases, respectively, from July 1995-September 1996. Another report, “Update of enterovirus infection in infants and children” states, in a section titled “Viral meningitis,” that natural polioviruses were an important cause of viral meningitis before vaccination (cases were called “nonparalytic poliomyelitis”). Now, “rare” cases of viral meningitis are attributed to the attenuated polioviruses in vaccines, in both vaccine recipients and their contacts.’
http://www.whale.to/a/meningitis.html

Meninjugate, the other Meningitis C vaccine now under scrutiny, was originally manufactured by Chiron, a subsidiary of Novartis Pharmaceuticals. According to independent investigative reporter Liam Scheff of The Observer, this major vaccine distributor forcibly injected black, Hispanic and poor children with experimental vaccines known to cause genetic mutation, organ failure, bone marrow death, bodily deformations, brain damage and fatal skin disorders in New York’s Washington Heights’ Incarnation Children’s Center, a former convent house during 2004 & previously.

Novartis announces agreement to acquire remaining stake in Chiron/October, 2005
http://dominoext.novartis.com/NC/NCPRRE01.nsf/44aff02a639be034c1256b4b007b5f4d/3a67fd6e65259747c12570ab0045894e/$FILE/Chiron-%20EN%20-%2031.10_FINAL.pdf

Chiron Involved in Inhuman Experiments – ‘In New York’s Washington Heights is a 4-story brick building called Incarnation Children’s Center (ICC). This former convent houses a revolving stable of children who’ve been removed from their own homes by the Agency for Child Services. These children are black, Hispanic and poor. Many of their mothers had a history of drug abuse and have died. Once taken into ICC, the children become subjects of drug trials sponsored by NIAID (National Institute of Allergies and Infectious Disease, a division of the NIH), NICHD (the National Institute of Child Health and Human Development) in conjunction with some of the world’s largest pharmaceutical companies – GlaxoSmithKline, Pfizer, Genentech, Chiron/Biocine and others.

The drugs being given to the children are toxic – they’re known to cause genetic mutation, organ failure, bone marrow death, bodily deformations, brain damage and fatal skin disorders. If the children refuse the drugs, they’re held down and have them force fed. If the children continue to resist, they’re taken to Columbia Presbyterian hospital where a surgeon puts a plastic tube through their abdominal wall into their stomachs. From then on, the drugs are injected directly into their intestines.’      Liam Scheff, The Observer, 2004-10-12
http://www.whale.to/a/ch2.html

NOTE: Investigative journalism of Scheff’s caliber rarely surfaces in the mainstream press. The incarceration & exploitation of helpless children, by a powerful vaccine manufacturer, for purposes of illegal product testing must not go unpunished. Novartis cannot shield these crimes committed in the light of day. It is always the disenfranchised, the institutionalized, prisoners of the State, mentally challenged individuals cast into the waste bin by society, children set adrift into the clutches of Child Protection Services, who inadvertently wind up the victims of these callous acts. We must rise up unanimously and be their voice; for they have been silenced against their will.

4, 5 & 6. Measles, Mumps, Rubella Vaccine

M-M-R II is a sterile lyophilized preparation of (1) ATTENUVAX* (Measles Virus Vaccine Live), a more attenuated line of measles virus, derived from Enders’ attenuated Edmonston strain and propagated in chick embryo cell culture; (2) MUMPSVAX* (Mumps Virus Vaccine Live), the Jeryl Lynn** (B level) strain of mumps virus propagated in chick embryo cell culture; and (3) MERUVAX* II (Rubella Virus Vaccine Live), the Wistar RA 27/3 strain of live attenuated rubella virus propagated in WI-38 human diploid lung fibroblasts.1,2
The growth medium for measles and mumps is Medium 199 (a buffered salt solution containing vitamins and amino acids and supplemented with fetal bovine serum) containing SPGA (sucrose, phosphate, glutamate, and recombinant human albumin) as stabilizer and neomycin. The growth medium for rubella is Minimum Essential Medium (MEM) [a buffered salt solution containing vitamins and amino acids and supplemented with fetal bovine serum] containing recombinant human albumin and neomycin. Sorbitol and hydrolyzed gelatin stabilizer are added to the individual virus harvests.
The cells, virus pools, and fetal bovine serum are all screened for the absence of adventitious agents.
The reconstituted vaccine is for subcutaneous administration. Each 0.5 mL dose contains not less than 1,000 TCID50 (tissue culture infectious doses) of measles virus; 12,500 TCID50 of mumps virus; and 1,000 TCID50 of rubella virus. Each dose of the vaccine is calculated to contain sorbitol (14.5 mg), sodium phosphate, sucrose (1.9 mg), sodium chloride, hydrolyzed gelatin (14.5 mg), recombinant human albumin (≤0.3 mg), fetal bovine serum (<1 ppm), other buffer and media ingredients and approximately 25 mcg of neomycin.
http://www.merck.com/product/usa/pi_circulars/m/mmr_ii/mmr_ii_pi.pdf

NOTE: Hazards include ATTENUVAX* Measles, MUMPSVAX* Mumps & MERUVAX* II Rubella (multiple live viruses), fetal bovine serum (Human aborted fetal diploid cells), Neomycin (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).

Dr. Andrew Wakefield’s early study indicating Inflammatory Bowel Disease in children with Autism & the MMR shot l’Ileal-lymphoid-nodular hyperplasia, non-specific colitis, and pervasive developmental disorder in children’
http://www.generationrescue.org/pdf/wakefield2.pdf

‘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

Risk of aseptic meningitis after measles, mumps,and rubella vaccine in UK children: ‘The study confirmed that the true risk was substantially higher than suggested by case reports from paediatricians, probably about 1 in 11 000 doses. However, the possibility that the aseptic meningitis induced by vaccination was largely asymptomatic and a chance laboratory finding in children investigated for other clinical conditions, particularly febrile convulsions, could not be excluded. Comparison of national reports of virus-positive mumps meningitis cases before and after the introduction of this vaccine indicated that the risk from wild mumps was about 4-fold higher than from vaccine. Altogether, 28 vaccine-associated cases were identified, all in recipients of vaccines containing the Urabe mumps strain. The absence of cases in recipients of vaccine containing the Jeryl Lynn strain, despite its 14% market share, suggested a higher risk from Urabe vaccine.’
http://www.thelancet.com/journals/lancet/article/PII0140-6736%2893%2991069-X/abstract

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

“Mumps meningitis following measles, mumps, and rubella immunisation [letter]” (The Lancet, vol. 2, July 8, 1989, p. 98; comments in vol. 2, August 12, 1989, pp. 394-5; vol. 2, September 16, 1989, p. 677): in the primary letter, mumps meningitis was reported in a three-year-old girl twenty-one days after measles, mumps, and rubella (MMR) immunization. The child exhibited lethargy, vomiting, headache, dry cough, fever, irritability, and meningeal irritation. There was no known exposure to the measles, mumps or rubella natural infections. No bacterial or other infections were found. In the August 12 issue of Lancet, a West German physician reported, also in a letter, a two-year-old boy with mumps meningitis twenty-one days following a different manufacturer’s MMR vaccine. There was no exposure to natural mumps virus. The author of August 12 concludes, “The incubation time for mumps is about 21 days. In some patients, time-lag between immunisation and manifestation of meningitis was very close to 3 weeks, without known previous mumps contacts. These facts strongly suggest that some patients may have had vaccine mumps meningitis, and not wild mumps infection.” In the September 16 issue of Lancet, two British physicians report two 16-month-old boys with mumps meningitis admitted to the hospital 18 and 19 days following MMR immunization. Mumps virus was isolated from cerebrospinal fluid of both boys. One boy did not exhibit a rise in mumps antibodies in spite of vaccination and post-vaccinal meningitis. [Other vaccinal mumps meningitis citations: “Mumps meningitis, possibly vaccine related.”
http://www.whale.to/a/meningitis.html

Database of 557 official reports of adverse side effects to vaccinations received in 2010 (including H1N1, MMR, DPT, Hepatitis A/B, HPV, Polio, Haemophilus B, TBE, Meningococcal & Rotavirus shots)
http://www.impfschaden.info/en/vaccine-damage-reports-2010.html

New independent research presented at the 2010 Pediatric Academic Societies Annual Meeting in Vancouver, Canada confirms unequivocally the findings of Dr Andrew Wakefield’s 1998 Lancet paper of an association between autism and serious gastrointestinal disease in children. The new study was conducted by the Autism Speaks Autism Treatment Network and covered data from 15 treatment and research centers in the United States and Canada.  Of 1185 children aged 2 to18 years with an autistic condition 45% were reported to have GI symptoms. Abdominal pain was most common (59%) followed by constipation (51%), diarrhea (43%), other (40%), nausea (31%) and bloating (26%). Reports of GI symptoms increased with age.  Sleep problems occurred in 70% of children with than those without GI symptoms (30%).  The problems affected all children regardless of gender, ethnic background or intelligence.
http://childhealthsafety.wordpress.com/2010/05/06/wakefield%E2%80%99s-lancet%C2%A0paper%C2%A0vindicated/

Another UK based study also legitimized Wakefield’s research linking Autism & Inflammatory Bowel Disease; identifying a characteristic chemical signature/marker (metabolic abnormalities) in their urine. “The signature that comes up is related to gut bacteria,” Dr. Nicholson, Imperial College
http://www.newscientist.com/article/dn19011-gut-bacteria-may-contribute-to-autism.html?DCMP=OTC-rss&nsref=online-news

‘Kaye (BMJ lead investigator in the case against Wakefield) and colleagues’ analysis of the GPRD, a database that currently holds records on 3 million patients from general practices throughout the United Kingdom, revealed that the number of children receiving the triple inoculation held high and steady, with coverage at over 95% in successive birth cohorts. Rates of autism diagnosis, however, increased nearly 4-fold over time among 2- to 5-year-old boys born in 1988-1993.

The investigators write, “If the MMR vaccine were a major cause of the increasing incidence of autism, then the risk of autism in successive birth cohorts would be expected to stop rising within a few years of the vaccine being in full use.” Since the numbers of children found to have autism continued to increase regardless of how many received immunizations, Kaye and colleagues conclude that there is little evidence to indicate an association between vaccine and diagnosis. They speculate that the marked growth in reported incidence may come as a result of changes in diagnostic criteria, increased awareness of the condition among parents and general practitioners, or environmental factors not yet identified.’ http://www.medscape.com/viewarticle/411252

Aluminum toxicity & synergy effect (vaccine derived) as it relates to the body –

Aluminium: A silvery-white, ductile metallic element, the most abundant in the earth’s crust but found only in combination, chiefly in bauxite. Having good conductive and thermal properties, it is used to form many hard, light, corrosion-resistant alloys. Atomic number 13; atomic weight 26.98; melting point 660.2°C; boiling point 2,467°C; specific gravity 2.69; valence 3.

‘In 1927, Dr. Victor Vaughn, a toxicologist with the University of Michigan, testified before the Federal Trade Commission that “all salts of aluminum are poisonous when injected subcutaneously or intravenously”. According to the American Academy of Pediatrics, “Aluminum is now being implicated as interfering with a variety of cellular & metabolic processes in the nervous system and in other tissues. In 1997 The New England Journal of Medicine published data showing that premature babies injected with aluminum build up toxic levels in the blood, bones and brain, and that aluminum toxicity can lead to neurological damage, including mental handicaps at 18 months of age.” Neil Miller

Aluminum is a highly conductive “electropositive” metal. The human body is also charged with electromagnetic, bio-conductive energy. Essentially we are bio-electric beings. Certain storehouses are concentrated with higher degrees of “conductivity”; in particular the brain which consists primarily of neurons.

As Dr. Gary Tunsky illustrates, Aluminum is a coagulant which inherently binds to any toxin in its path. In fact its primarily industrial use is to bond debris in water treatment centers; whereupon it is then scraped out of the cylinders during the filtration process.

“Your blood has no method of excretion; Heavy metals & live viruses, formaldehyde are redistributed by the blood to areas of fatty tissue (highly conductive/electrical tissues) – found in the gray matter of the brain, the mylene sheathe, 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

The viscosity of this toxic sludge resulting from vaccines which accumulates in the organs (ie. heart, liver, kidney), joints, meninges, intestines, along the neural pathways, veins & capillaries interlacing the entire body (resulting from “stagnant” blood), is comparable to the black paste-like build-up found over time in the lining of your drains – especially in terms of its impact on your vital health.

Within 72 hours of oxygen deprivation any cell will become cancerous. Cancer cells thrive in an oxygen-deprived environment. This will occur when bio-conductive aluminum (consisting of live virus, antibiotic, heavy metal, detergent coagulated sludge) clogs the vast network of arterial veins & capillaries, inducing Ischemia.

‘Oxygen–glucose deprivation resulted in expression of apoptotic and necrotic cell death phenotypes, especially in neurons.’ ‘Following 72 hours incubation in the presence of 0.3% O2, cells were labeled with Annexin V/PI and the level of cell death was measured by flow cytometry. In 6 independent experiments, hypoxia increased levels of Annexin V-positive OC316 cells from 5.3 ± 1.0% to 19.2 ± 2.8% cell death under these conditions had predominant features of late apoptosis.’ Meanwhile bad food choices (casein, gluten, poly-saturated fats, iodized salts, sugars) produce a breeding ground in the body for long-term infections, thyroid disorder, disease & vaccine derived viruses. All viruses thrive in a non-alkaline, acidic environment. Overall the impact of of Ischemia & excessive alkalinity serve as a double-edged sword, critically damaging our vital health.

‘The human blood is a colloidal suspension. Proteins, Amino acids, heavy metals etc., are carried in suspension within the blood as a function of the net negative charge within the system. Drop the net negative charge, flow pressures in tiny end blood vessel “pipes” will start to sludge, agglomerate, and increase viscosity of blood in circumscribed microscopic vascular areas.

This “sludging” is activated when Aluminum (64 times more positive than colloidal blood products are negative) interacts with Hemoglobin in flow, in the negatively charged environment. This causes the negatively charged blood products to “attract” towards the larger, more massive positively charged Aluminum, causing clumping or “sludging”. This restricts blood flow, and it changes the Zeta Potential to change from -15mv (minus 15 milivolts) towards -10 mv (minus 10 milivolts), or possibly closer to zero. This is an increase in Zeta Potential, from a negatively charge towards neutral. (This is somewhat analogous to a change in state of water as it turns to ice – it’s a change in viscosity, affecting blood flow).

Agglomerates of sludged blood products cannot traverse microscopic blood vessels designed to carry oxygen transporting red blood cells, in single file. Capillary blood vessels oriented against gravity are uniquely susceptible. Forward blood flow momentum is a function of the negative charge and “spin” in fluid dynamics which keeps particles with mass separated from one another. For the brain, and body, this causes hypoxia (low oxygen), anoxia (no oxygen) and ischemia (impaired blood flow). This is bodily harm when vaccine induced.’ Dr. Andrew Moulden

The US Food & Drug Administration ‘Drug Labeling Regulations Guide’ states unequivocally,

“Aluminum may reach toxic levels with prolonged parenteral administration if kidney function is impaired. Premature neonates are particularly at risk because their kidneys are immature, and they require large amounts of calcium and phosphate solutions, which contain aluminum. Research indicates that patients with impaired kidney function, including premature neonates, who receive parenteral levels of aluminum at greater than 4 to 5 [micro]g/kg/day accumulate aluminum at levels associated with central nervous system and bone toxicity. Tissue loading may occur at even lower rates of administration.” FDA

This means that for a 6 pound baby, 11-14 mcg would be toxic. The Hepatitis B vaccine given at birth contains 250 mcg of aluminum – 20 times higher than safety levels allow. Babies weigh about 12 pounds (5.5 kg) at 2 months of age when they receive 1225 mcg of aluminum from their vaccines – 50 times higher than safety levels.’ Currently children are getting 17 shots containing aluminum, a quadrupling of the amount given since the 1970’s. It is found in Hepatitis A, Hepatitis B, DTaP (diphtheria, tetanus, pertussis), MMR, Hib, Pneumococcal & Gardasil (HPV) vaccines.

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. ‘

Aluminum, combined with other ingredients commonly added to vaccines, will trigger more rapid & profound cell toxicity. Mercury, another devastating neurotoxin & one of the few liquid elements, actually binds with hemoglobin, which is responsible for oxygen transport to the tissues. In addition it “inhibits the regulation of brain glutamate levels, triggers excitotoxicity, increases brain free radicals and lipid peroxidation products, inhibits critical brain enzymes, inhibits antioxidant enzymes and impairs DNA repair ability”. Dr. Boyd Hayley performed a synergy experiment using aluminum hydroxide, mercury & neomycin (antibiotic associated with Kidney Failure, hazardous to a fetus). The results indicated a 75% acceleration in cell deaths when all 3 ingredients were combined.

Additionally, Polysorbate 80 or ‘Tween 80‘ is a type of detergent stabilizer commonly found in vaccines; which is linked to infertility & severe allergic reactions (ie. Anaphylaxis). ‘Neonatal female rats were injected with Tween 80 after birth. Treatment accelerated maturation, prolonged the oestrus cycle & induced persistent vaginal oestrus. Ovaries were without corpora lutea & had degenerative follicies.‘ Based on this verifiable clinical data no such toxin should ever, under any circumstances, be injected into a pregnant woman. Despite such conclusive evidence of its implications on female fertility,

Polysorbate 80 is, in fact, added to many current vaccines including: HPV (Gardasil/Cervavix), DTaP (Infanrix, Tripedia), DTaP-IPV (Kinrix), DTaP/Hib (TriHIBit), DTaP-HepB-IPV (Pediarix), DtaP-IPV/Hib (Pentacel), Hep A (Havrix). 2009’s H1N1 ‘Swine Flu’ vaccine (produced by GlaxoSmithKline (Pandemrix/Arepanrix), Novartis (Focetria) & Baxter Pharmaceuticals (Celvapan), widely promoted as a mandatory safety precaution for ALL pregnant women, contained this ingredient; yet another glaring red flag to be considered.

“Polysorbate 80 was identified as the causative agent for the anaphylactoid reaction of nonimmunologic origin in the patient. Polysorbate 80 is a ubiquitously used solubilizing agent that can cause severe nonimmunologic anaphylactoid reactions.” Department of Dermatology, University of Aachen, Aachen, Germany

Specific role of polysorbate 80 coating on the targeting of nanoparticles to the brain (causes a blood/brain barrier breach) “Partial coverage was enough for Tween-80 coating to play a specific role in brain targeting of nanoparticles; concerned with the interaction between T-80 coating and brain micro-vessel endothelial cells. Therefore, the specific role of T-80 coating on nanoparticles in brain targeting was confirmed.” Department of Material Science and Engineering, Huazhong University of Science and Technology, China Study, 2003

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. 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.’ Food & Drug Administration

‘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
http://www.vacinfo.org/Aluminum%20in%20Vaccines,%20Free%20ebook.pdf

‘Aluminum hydroxide injections lead to motor deficits and motor neuron degeneration’
http://www.bauernverstand.ch/images/bt_chris_shaw2009_englisch.pdf

A role for the body burden of aluminium in vaccine-associated macrophagic myofasciitis and chronic fatigue syndrome
http://www.theoneclickgroup.co.uk/documents/vaccines/Vaccine%20Aluminium%20In%20CFS.pdf

Vaccine derived toxicity triggers intense cytokine reactions in children with Autism  – Neuroglial activation and neuroinflammation in the brain of patients with autism: ‘Active neuroinflammatory process in the cerebral cortex, white matter & cerebellum of autistic patients, marked activation of microglia & astroglia. Cytokine profiling indicated that macrophage chemoattractant protein (MCP)-1 & tumor growth factor-beta1, derived from neuroglia, were most prevalent cytokines in brain tissues.’
http://www.ncbi.nlm.nih.gov/pubmed/15546155

“It seems clear that any latent infection, particularly when accompanied by transient bacteraemia or viraemia, may be wakened into activity by the disturbing effect on the tissue resistance of various factors, among which vaccines and certain medicaments are prominent. Ideally, vaccination against any disease should be preceded by a survey of the patient’s medical history and a simple physical examination to detect signs of any obvious infection. Mass vaccination, in which this is impossible, is bound to be a hazardous procedure and is bound to be followed by undesirable consequences of one sort or another.” Sir Graham Wilson renowned medical bacteriologist & author of “The Hazards of Immunisation”, 1967

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http://vaccineresistancemovement.org/?page_id=5463

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VRM : Former Pharmaceutical Representative Gwen Olsen Exposes Systemic Industry Fraud
http://vaccineresistancemovement.org/?p=5920

VRM: Britain’s National Health Service – Criminal Syndicate Swindling Billions While Rapidly Destroying Health Care System
http://vaccineresistancemovement.org/?p=4986

VRM: UK Institutes Brand of Medical Martial Law With ‘Super-Vaccination’ Day
http://vaccineresistancemovement.org/?p=4986

VRM : The Awakening Has Begun
http://vaccineresistancemovement.org/?p=6469

VRM: Medical Martial Law In The US – Sleeping Giant Of Tyranny
http://vaccineresistancemovement.org/?p=5865

VRM : Multi-Virus Vaccine Quinvaxem Proving Deadly
http://vaccineresistancemovement.org/?p=5219

VRM: New Generation Cancer Vaccine Will Cause Infertility
http://vaccineresistancemovement.org/?p=5311

VRM: CDC-Gate Exposes A Trail of Fraud Behind Autism Studies
http://vaccineresistancemovement.org/?p=5743

VRM : Squaline – The Military Agenda Comes Home
http://vaccineresistancemovement.org/?p=1797

VRM Live – 01/28/11: Vaccine Resistance Movement founder Joel Lord discusses Synthetic Genomics, cloned cell vaccine technology & the death of natural immunity, gutter journalism & Dr. Wakefield’s imminent vindication with ‘Truth to Power’ host Paul Mabelis.
http://www.blogtalkradio.com/empradio/2011/01/28/truth-to-power-thursday

VRM Live – 11/04/10: Vaccine Resistance Movement founder Joel Lord lays out the whole vaccine process with Paul Mabelis; including heavy metal toxicity, synergy, pregnancy issues & the basic principles of natural health at risk.
http://www.blogtalkradio.com/show.aspx?userurl=empradio&year=2010&month=11&day=05&url=truth-to-power-thursday

VRM Live – 09/24/10: Vaccine Resistance Movement Founder Joel Lord & activist/radio host Jesse Calhoun lay it all out tonite. Topics include the VRM Worldwide Autism Study, Scientific/Medical dictatorship, Natural Rights & Vaccine Industry fraud exposed. Special thanks to host Paul Mabelis.
http://www.blogtalkradio.com/empradio/2010/09/24/truth-to-power-thursday

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