As of January 1st, 2011, all children in the UK, upon reaching the age of 1, will be subject to a one stop, 6 vaccine assault. In what is being labeled ‘Super-vaccination’ day, babies will now get a series of 3 injections in one visit, a combination of the Measles, Mumps, Rubella triple live virus shot, the Meningitis C & Haemophilus influenzae type b (Hib) vaccines; in addition to the Pneumococcal Conjugate Vaccine (PCV); a series normally administered gradually over a 4 week period.
While the immediate Gov’t position offers parents an opt out clause, the trend toward combination ’super-vaccines’ is particularly worrisome; indicative of a medical system in serious damage control. This program constitutes, in essence, a nationwide clinical trial on the population; the most drastic mass vaccination experiment in history, targeting babies at a critical stage of early development.
“Toddlers are to be inoculated against six diseases at once in a bid to boost vaccination rates, the Government revealed yesterday. The chief medical officer has told GPs to give the vaccines – including the MMR jab – during a single surgery visit once a baby has passed his or her first birthday. The ‘super-vaccination’ day will involve three injections to protect against measles, mumps, rubella, two forms of meningitis & bacteria that can cause pneumonia.
A spokesman (for The Department of Health) said: ‘Independent scientific research has shown that this is completely safe and effective.”
British national health “authorities”, consisting of an adjunct ‘joint committee on vaccination and immunisation’, have given the radical program a green light based on so called ‘detailed interviews with a small number of mothers and fathers’; seemingly based on the criteria of their unspecified support alone – a flimsy justification without any substantial universal-type survey of the country’s families affected. This runs counter to a growing level of awareness in the world community of the imminent dangers posed by injecting various multiple live (or otherwise attenuated) viruses, heavy metals & other toxic excipients simultaneously into the human body at such a vulnerable stage of an infant’s development.
The British government has unanimously declared that the change would be ‘acceptable to parents’. This declaration flies in the face of ample, documented medical research indicating serious toxicity problems, physiological trauma & neuro-developmental disorders commonly associated with vaccine uptake; including mounting evidence of family victories in vaccine courts around the world.
The public response to this sweeping change in immunization protocol hinges on a thorough, unbiased dissemination of the risks associated when introducing 6 viruses simultaneously into body via a subcutaneous route. Increasingly, the gap between those educated on vaccine toxicity & the majority susceptible to Media-Government-Industry promulgated persuasion is narrowing. It is common knowledge in medical circles that 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 situated at these junctures; the natural first line of defence. Vaccines are injected into deep muscle tissue, a route which literally bypasses one’s natural barriers altogether. Thus the body is left vulnerable to live viruses & heavy metals. Vaccine distributors would rather you ignore these fundamental issues, to blindly trust in their corporate financed, “expert” panels of knowledge, backed by exclusive insider research, to swallow the litany of Media fed propaganda, and obediently join the queues with the rest of the flock at your local vaccine clinic, to roll up your sleeve. However, a grassroots vaccine resistance movement has arisen in the eleventh hour to awaken the masses to this imminent crisis.
According to Gwen Olsen, a 20 year veteran Pharmaceutical Representative turned whistle-blower, “The Pharmaceutical Industry is in the business of disease maintenance & symptom management. They are not in the business to cure Cancer, to cure Alzheimer’s, to cure heart disease, because if they were they would be in the business of putting themselves out of business; and that in fact doesn’t make sense. The Pharmaceutical Industry makes 5-6 times the amount of money of any of the other Fortune 500 companies in the United States of America. They are not going to easily or readily give up that income. You’re never going to have anyone come to you and tell you that the drugs are always tried against a placebo (sugar pill) in clinical trials. In fact many drugs are found not to be more efficacious than the sugar pill.”
The New England Journal of Medicine, a preeminent Medical Industry source for research, has just laid out a sociological blueprint strategy paper for determining the degrees of persuasion needed to ensure widespread compliance of the ‘herd’. Clearly the impact of the anti-vaccine movement spreading knowledge, coupled with a growing distrust of government & Big Pharma, has vaccine manufacturers & health departments everywhere scrambling.
‘Despite the importance of public acceptance, the science that would clarify the best ways of informing and motivating the public is severely underdeveloped. How can indifferent or negative attitudes toward vaccination be changed? A quick look at publicly funded research on the topic of influenza and influenza vaccination, made possible by the Research Portfolio Online Reporting Tool from the National Institutes of Health, indicates that over the past decade more than 95% of funding has been devoted to biomedical topics rather than to social and behavioral science. Clearly, cutting-edge laboratory science to enhance the safety and effectiveness of vaccines is vital to public health. But it is equally important to understand the forces that shape public views about the risks and benefits of vaccination. Without this knowledge, it will be impossible to translate biomedical advances into effective action.’
‘Increasing the public’s acceptance of vaccination may be more difficult than addressing the technical and scientific challenges involved. Survey data collected by RAND and others indicate that even at the outset of the pandemic, when fear of H1N1 influenza was widespread, less than half of all adults were willing to get vaccinated against it.’ NEJM
Babies as young as 6 months old are now routinely being inoculated for influenza at 6 months; a drastic intervention in early development; by the Medical purveyors’ own admittance, one intended to boost general rates for vaccine uptake. The strategy seems to be in provoking a wider swath of vaccine uptake, thus inevitably opening the floodgates to a greater exposure of the herd.
“We hope that the new recommendations promulgated by the Advisory Committee on Immunization Practices (ACIP) will help. Rather than focus on “high-risk groups,” as has been done in the past, the ACIP now recommends annual influenza vaccination for everyone 6 months of age or older.”
‘Influenza vaccine (seasonal). (Minimum age: 6 months for trivalent inactivated influenza vaccine [TIV]; 2 years for live, attenuated influenza vaccine [LAIV]) • Administer annually to children aged 6 months through 18 years.’ CDC Standard Immunization Schedule age 0-6 yrs
“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, CDC closed door meeting, 2000
Mainstream media routinely colludes with the Vaccine Industry, in terms of ferreting out negative press while cherry picking often rigged studies & data sponsored by vaccine manufacturers, designed to push their product on the public. They also play a key role in swaying the population through the use of fear mongering of headlines & the spreading of disinformation and/or exaggerated hype termed ’spin’. The dust is still settling from 2009’s alarmist Pandemic, an episode in history which marked a new low in gutter journalism.
Government also frequently manipulates media headlines behind the scenes, as revealed in this interview with Kathleen Sebelius, US secretary of the Department of Health and Human Services,
“There are groups out there that insist that vaccines are responsible for a variety of problems despite all scientific evidence to the contrary. We have reached out to media outlets to try to get them to not give the views of these people equal weight in their reporting to what science has shown and continues to show about the safety of vaccines.”
India recently experimented with a Pentavalent or 5 in 1 vaccine, combining Hepatitis B, Haemophilus influenza type B (Hib), Diphtheria, Pertussis & Tetanus (DPT), literally a tsunami of live viruses & heavy metals. the results were disastrous. 4 children from Lucknow, capital of northern Uttar Prudesh State, died “within minutes” from what was initially reported as the Measles and/or Bacillus Calmette-Guérin (Tuberculosis) vaccine. It now appears they may have been unwitting guinea pigs for a test model ’super vaccine’, a new Pentavalent vaccine combining Hepatitis B, Haemophilus influenza type B (Hib), Diphtheria, Pertussis & Tetanus (DPT). Literally a tsunami of live viruses & heavy metals.
“A campaign against the Haemophilus influenzae type b (Hib) vaccine in India launched by some medical professionals has delayed a government plan to introduce the vaccine through its free national immunisation programme for children.”
In Denver, Colorado, a similar test was conducted earlier this year. Unsuspecting children were administered a Quadrivalent vaccine, 4 shots injected simultaneously by nurses on call. Their immediate side effects are not currently known; but clearly there will be serious, long-term health implications for these tragic victims of the system.
Britain is entering hitherto unknown country with what is termed a Hexavalent vaccine, a 6 in 1 juggernaut. The consequences for babies who receive this toxic blast will undoubtedly be so severe, the press so damning, it may take years for the National Health Service (NHS) to dig out from under the weight of the inevitable series of vaccine court lawsuits which will be brought against them.
Precisely which vaccines are being included in this medley? What have we learned about the ingredients & the synergistic effects of heavy metal toxicity on the body?
1. Pneumococcal Conjugate Vaccine (PCV)
Prevenar 13® manufactured by Wyeth. Active ingredients – Each 0.5 mL dose contains: 2.2 μg of pneumococcal purified capsular polysaccharides for serotypes 1, 3, 4, 5, 6A, 7F, 9V, 14, 18C, 19A, 19F and 23F, 4.4 μg of pneumococcal purified capsular polysaccharides for serotype 6B. Each serotype is individually conjugated to non-toxic diphtheria CRM197 protein and adsorbed on aluminium phosphate (0.565 mg). Excipients: Succinic acid, polysorbate 80, aluminium phosphate, sodium chloride in water for injections.
NOTE: Hazards include pneumococcal purified capsular polysaccharides for serotypes (strands of attenuated DNA/RNA derived from multiple live viruses), polysorbate 80 (toxic detergent linked to infertility & severe allergic reactions (ie. Anaphylaxis) & aluminium phosphate (highly conductive heavy metal adjuvant or booster linked to Ischemia & a host of neuro-degenerative disorders including Alzheimer’s Disease)
‘The efficacy of Prevnar appears to be very limited – 7% fewer new earaches, and 0.1% fewer instances of invasive pneumococcal disease The studies done on Prevnar suggest that it may interfere with the efficacy of two other vaccines (pertussis and IPV) and could interfere with two more vaccines (MMR and Varicella).
The studies of efficacy of other vaccines in combination with Prevnar used numbers of children (n = 214, 47, 156, 0) that are statistically questionable in respect to the seven million children targeted to receive Prevnar. Prevnar is directed for administration to immune-suppressed children, a practice that apparently has not been studied for either safety or efficacy,’
“The alleged benefits for this new vaccine are greatly exaggerated and the risks are significant. The bacteria pneumococcus, with more than 90 serotypes, is a common pathogen. Though pneumococcus causes various diseases the carriage rate and serotype distribution rates in different groups are not know. Also, it is not known how pneumococcus transmutes itself into a pathogen. The role of pneumococcus in the microbiological balance is not known. It does contribute to 3,000 cases a year of meningitis, 50,000 a year of bacteremia, 500,000 cases of pneumonia, and seven million cases of otitis media or ear infections. With all of these unknowns, the vaccination of newborns with seven pneumococcal serotypes and possible eradication of those serotypes, is an uninformed experiment at best,” Dr. Erdem Cantekin, Ph.D., Professor of Otolaryngology, University of Pittsburgh.
2. Haemophilus influenzae type b Vaccine (Hib)
ActHIB® Haemophilus b Conjugate Vaccine manufactured by Sanofi Pasteur: The vaccine consists of the Haemophilus b capsular polysaccharide (polyribosyl-ribitol-phosphate, PRP), a high molecular weight polymer prepared from the Haemophilus influenzae type b (HiB) strain 1482 grown in a semi-synthetic medium, covalently bound to tetanus toxoid. (1) The lyophilized ActHIB vaccine powder and saline diluent contain no preservative.The tetanus toxoid is prepared by extraction, ammonium sulfate purification, and formalin inactivation of the toxin from cultures of Clostridium tetani (Harvard strain) grown in a modified Mueller and Miller medium. (2) Further manufacturing process steps reduce residual formaldehyde to levels below 0.5 micrograms (mcg) per dose by calculation. The toxoid is filter sterilized prior to the conjugation process. Potency of ActHIB vaccine is specified on each lot by limits on the content of PRP polysaccharide and protein in each dose and the proportion of polysaccharide and protein in the vaccine which is characterized as high molecular weight conjugate.
NOTE: Hazards include Haemophilus b capsular polysaccharide (strands of attenuated DNA/RNA derived from a live virus), Formalin or Formaldehyde, used as “a preservative & disinfectant” which causes proteins to irreversibly bind to your DNA, and is known to cause cancer, chronic bronchitis, eye irritation when exposed to the body’s immune system.
‘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.’
‘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.’
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.”
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.
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.’
‘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. ‘
“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.’
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
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
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. ‘Since the 2002 gradual phase-out of the Thimerosal Mercury in vaccines, the use of aluminum has increased by 20%. Babies receive multiple doses of aluminum-containing shots. For example the Hepatitis B vaccine (Energix-B) is given at birth, 2 and 6 months of age. Each dose contains 250 micrograms (mcg) of aluminum. The DTaP shot (Infanrix) is given at 2, 4, 6, and 15 months. Each dose contains 625 mcg of aluminum. the Hib vaccine (Pedvax) is given at 2, 4, and 12 months. Each dose contains 125 mcg of aluminum. The Hepatitis A vaccine (Havrix) is given at 12 and 18 months. each dose contains 250 mcg of aluminum. Thus babies who follow the CDC immunization schedule are injected with nearly 5000 mcg (50 mg) of aluminum by 18 months of age.‘ 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. Neomycin/Polymixin (antibiotic excipient in vaccines) & Polysorbate 80/Tween 80 (detergent excipient) 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. 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. 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 VRM: The Problem With Vaccines Part 2 – Synergistic Effect of Heavy Metal Toxicity On The Body http://vaccineresistancemovement.org/?p=6097 “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