![\"FluVaccine](\"http:\/\/vaccineresistancemovement.org\/wp-content\/uploads\/2011\/01\/FluVaccine-Clinics1.jpg\" "\\"FluVaccine")
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\u201cThere is no evidence that any vaccine thus far developed is effective in preventing or mitigating any attack of influenza. The producers of these vaccines know that they are worthless, but they go on selling them, anyway.\u201d J. Anthony Morris, Former Chief\u00a0 Vaccine Control Officer, FDA<\/strong><\/p>\n The Influenza virus itself is constantly mutating from year to year. While mainstream doctors are traditionally divided, several prominent Studies have come forward in recent years challenging the Status Quo on the efficacy of the sacrosanct Flu shot & awakened an increasingly distrustful public to the ineffectiveness and inherent danger of vaccines.<\/strong><\/p>\n ‘Over 200 viruses cause influenza and influenza-like illness which produce the same symptoms (fever, headache, aches and pains, cough and runny noses). Without laboratory tests, doctors cannot tell the two illnesses apart. Both last for days and rarely lead to death or serious illness. At best, vaccines might be effective against only influenza A and B, which represent about 10% of all circulating viruses. Each year, the World Health Organization recommends which viral strains should be included in vaccinations for the forthcoming season. Influenza vaccines have a modest effect in reducing influenza symptoms and working days lost. There is no evidence that they affect complications, such as pneumonia, or transmission<\/a>.’ The Cochrane Review<\/strong>\u00a0<\/strong><\/p>\n ‘Children and the elderly are the two age groups that appear to have the most complications following an influenza infection. In children under the age of two, the efficacy of inactivated vaccine was similar to placebo. Very little info\u2019 found on safety of inactivated vaccines in young children.’<\/a> The Cochrane Review\u00a0<\/strong><\/p>\n \u2018A \u201cperplexing\u201d Canadian study linking H1N1 to seasonal flu shots is throwing national influenza plans into disarray and testing public faith in gov\u2019t agencies responsible for protecting the nation\u2019s health. Study confounds infectious-disease experts in suggesting that people vaccinated against seasonal flu are twice as likely to catch swine flu. \u201cIt has confused things very badly,\u201d said Dr. Ethan Rubinstein, head of adult infectious diseases at the University of Manitoba. \u201cAnd it has certainly cost us credibility from the public because of conflicting recommendations. Until last week, there had always been much encouragement to get the seasonal flu vaccine.\u201d\u2019 \u2018Association between the 2008\u201309 Seasonal Influenza Vaccine and Pandemic H1N1 Illness during Spring\u2013Summer 2009: Four Observational Studies from Canada: \u2018Estimates from the sentinel and three other observational studies, involving a total of 1,226 laboratory-confirmed pH1N1 cases and 1,505 controls, indicated that prior receipt of 2008\u201309 TIV (trivalent inactivated influenza vaccine aka regular flu shot) was associated with increased risk of medically attended pH1N1 illness during spring\u2013summer 2009\u2032<\/strong> \u201cBecause the influenza virus genome is segmented, coinfection of a single host cell with two or more different influenza viruses can result in a reassortment (shuffling) of their genetic material. The antigenic shift can lead to a pandemic if the resulting progeny virus contains an HA protein to which humans have no preexisting immunity, if it has an efficient replication-competent set of internal genes, and if it can readily spread from human to human.\u201d <\/strong> Dr. Antony Fauci<\/a>, director of the National Institute of Allergy & Infectious Diseases (co-patent holder of \u201cIImmunologic enhancement with intermittent interleukin-2 therapy<\/a>\u201d described as being central to gene therapies and the future of \u201cgeneto-pharmaceuticals\u201d)<\/strong><\/p>\n Universal Flu Vaccine will unleash a new cats cradle of mutagenic viruses; which in turn will spawn a new wave of counter shots.<\/strong> – ‘Researchers at Oxford University have “successfully” tested a universal flu vaccine, an approach that could be used to combat all strains of the flu with a single shot. The team gave the vaccine to 11 healthy volunteers, then infected them with H3N2 influenza A, a flu strain that was identified in Wisconsin in 2005. “We did get an indication that the vaccine was protecting people.”‘ Cells for which specific knowledge of the transforming event exists (and can be shown not to be a virus that persists in the cells) may be more easily characterized than cells for which there is no specific knowledge of the transforming event (which could theoretically have been due to an infection with a known or an unknown virus).<\/strong><\/p>\n In addition to assessing the possibility of contamination of cell substrates with infectious virus, it is important to consider other agents such as the agent of TSE (Transmissible Spongiform Encephalopathy). There are several mechanisms by which vaccine cell substrates, including neoplastic cells, could theoretically become infected with a TSE agent.\u2019 US Food & Drug Administration 1 Flu deaths are attributed primarily to bacterial pneumonia triggered by the flu symptoms. The flu itself cannot kill you.<\/strong><\/p>\n 2 Most victims of the flu are those 65 years and older.<\/strong><\/p>\n 3 In almost every instance a compromised immune system is a key factor in those victims who succumb to the flu.<\/strong><\/p>\n It is significant that mass vaccinations for children under 5 only began in 2003. That year saw a 10 fold increase in flu deaths among children 1-4 years of age. (Age Group category \u2013 Page 14) – See Trend Report on Pneumonia and Influenza<\/a><\/strong>\u00a0<\/strong><\/p>\n \u201cEthyl Mercury: Organic mercury attached to short carbon chain, converts to inorganic mercury quicker than Methyl Mercury \u2013 in about 7 days. Once entered into the brain it becomes trapped. The timing makes the poison.\u00a0 Thimerosal in vaccines: 0.01% = 50,000 micrograms\/litre (50% mercury content, 250 times higher than the EPA safe limit). Amount of <\/strong>Hazardous waste<\/strong> <\/strong>in vaccines: 25,000 times higher than EPA safe limit <\/strong>(<\/strong>200 parts per billion = hazardous waste. Drinking water: 2.5 billion parts per billion = toxic waste)<\/strong>.\u201d Dr. David Ayoub<\/a><\/strong><\/p>\n Studies have shown that mercury is taken up in the periphery by all nerve endings and rapidly transported inside the axon of the nerves (axonal transport) to the spinal cord & brainstem.<\/a> 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.<\/strong><\/p>\n 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\u2019s blood<\/a>. <\/strong><\/p>\n \u201cThe 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 neurodegenerative diseases is the most significant, with the references numbering 1,445. <\/strong><\/p>\n 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\u2019s 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\u2019t have to look far in understanding how a heavy metal like mercury can eventually lead one to cancer\u2019s door.\u201d Dr. Rashid Buttar\/Center for Advanced Medicine & Clinical Research \u201cInjecting 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.\u201d \u2018Included in the ingredients are two antibiotics, Neomycin and Polymyxin B Sulphate. Both are noted for serious side effects, predominantly kidney failure. It is warned both these antibiotics not be used by pregnant women. Neomycin is in the FDA pregnancy category D. This means that it is known to be harmful to an unborn baby. In the \u201cfirst tier\u201d of candidates to receive this unregistered, unapproved vaccine, pregnant women are on top of the list. Beta-Propiolactone is another listed ingredient. Ranked as one of the most hazardous compounds (worst 10%) to humans and \u201creasonably expected to be a human carcinogen\u201d (International Agency for Research on Cancer \u2013 IARC, 1999). \u0392eta-Propiolactone is a disinfectant. Panvax is formulated using chick embryos (Ovalbumin). People who suffer allergy to eggs or anaphylactic reactions may experience problems.\u2019 \u2018The Australian is reporting that clinical tests were never carried out on this particular vaccine, which was a first-time combination of seasonal flu with Panvax, a vaccine against the H1N1 strain. Australia was the first country to use this type of vaccine, the report said. Panvax was tested on 400 children before its release last year, but the combined shot was not subjected to any clinical trials.\u2019 Panvax: Package insert – Early vaccine trauma report from Australia (high temperatures & febrile convulsions<\/a>) \u2013 The Australian Health Minister, Kim Hames, says 45 children have been taken to hospital suffering high temperatures and febrile convulsions after receiving the vaccination. Dr Hames says the program will be suspended until the department finishes its investigation. He says parents who have had their children vaccinated should take precautions.\u201dIf it\u2019s longer than 12 hours ago then there is no risk. But if it\u2019s in the last 12 hours they should make sure that they give their child paracetamol and then take every effort to make sure that the temperature of their child is settled.\u201d Febrile convulsions occur in young children when there is a rapid increase in their body temperature. It affects up to 1 in 20 children between the ages of one and four but can affect children between six months and about five years old.<\/strong><\/p>\n Australian vaccine scandal worsening \u2013 250 reports of adverse reactions \u2013 a figure experts and parents fear is being severely underestimated. It has became a hot topic in online parenting forums such as \u2018Essential Baby\u2019, where hundreds of mothers and fathers have expressed their fears and detailed nightmare stories of their children\u2019s reactions.<\/strong><\/p>\n Perth mother Marrisa Moir reports her two-year-old son began gagging and squealing in the bath about four hours after having the flu vaccine on April 9. \u201cI grabbed him out of the bath and then he started shaking uncontrollably. He couldn\u2019t stand or hold anything, he was shaking that much. \u201cHe curled his arms over his chest, kept gagging and letting out squeals. I had no idea what the hell was going on.\u201d Afluria (produced by Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.): Package Insert \u2013 5 mL multi-dose vial. Thimerosal, a mercury derivative, is added as a preservative; each 0.5 mL dose contains 24.5 mcg of mercury; contraindicated in individuals with known hypersensitivity to eggs, neomycin, or polymyxin.<\/strong><\/p>\n Administration of CSL\u2019s 2010 Southern Hemisphere influenza vaccine has been associated with increased post-marketing reports of fever and febrile seizures in children predominantly below the age of 5 years as compared to previous years. If Guillain-Barr\u00e9 Syndrome (GBS) has occurred within 6 weeks of previous influenza vaccination, the decision to give AFLURIA should be based on careful consideration of the potential benefits and risks. Immunocompromised persons may have a diminished immune response to Afluria. Afluria\u00ae \u2013 Package Insert The main target group for this shot encompasses 6 months through <\/strong> \u2265<\/strong>65 years of age. <\/strong>Anyone to speak of with <\/strong>Diabetes, Heart & Pulmonary disfunction, Cancer, Asthma, Anemia, virtually anyone with pre-existing medical conditions or compromised immune systems & health care workers, all being pressured to take this shot. Health Canada has clearly abandoned its role. <\/strong><\/p>\n ‘Fluviral’ (Manufactured for Canada): Analysis of ingredients –<\/strong><\/p>\n Multiple viruses (heat-treated\/total of 45 micrograms) including 2009\u2019s H1N1 sub-units – Thimerosal (100\u03bcg\/mL) –\u00a0 50 micrograms of Thimerosal mercury per shot (0.5 microgram\/ 0.5 mL dose\u00a0 x 100\u03bcg\/mL). Based on EPA standards this constitutes a safe level for a 1100 pound adult.<\/strong><\/p>\n Formaldehyde \u2013 used as \u201ca preservative & disinfectant\u201d, binds to the proteins in your DNA, known to cause cancer, chronic bronchitis, eye irritation when exposed to the body\u2019s immune system.<\/strong><\/p>\n Potassium Chloride \u2013 Used as part of a phosphate buffered saline in the shot. The majority of the potassium chloride produced is used for making fertilizer<\/a>, 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 <\/a>(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:\u00a0 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.<\/strong><\/p>\n 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.<\/a> 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 <\/a>and central nervous system effects.<\/a> The toxicity of phosphates is because of their ability to sequester calcium.<\/strong><\/p>\n Note: sodium Phosphate Dibasic Heptahydrate (also know as Disodium Hydrogen Phosphate<\/a>) \u2013 Chemical composition includes Fluoride\/50 mg\/kg, Arsenic\/50 mg\/kg, Lead\/10 ppm<\/a><\/strong><\/p>\n Sodium Deoxycholate: A detergent added to new generation of \u2018Split Vaccines\u2019 to modify the whole virus which causes cell death and symptoms such as burning, redness, and swelling. <\/a>It has been shown to weaken the blood-brain-barrier (BBB) and subsequently activate seizures.\u00a0 It demonstrates synergistic toxicity \u2014 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.<\/a><\/strong><\/p>\n Fluviral\u00ae (2010-2011) Package Insert UK Gov’t reluctantly bans 2010-11 Flu vaccine for \u2018under-fives\u2019: <\/strong>‘Ministers and senior Government advisers last night ruled that the immunisation programme for those aged six months to five years \u2013 which was quietly cancelled earlier this year \u2013 would not have significant \u2018gain\u2019. The decision came after the Government\u2019s interim chief medical officer, Professor Dame Sally Davies, held crisis talks with advisers from the Joint Committee on Vaccination and Immunisation over whether the jab should be offered to under-fives. Britain had already suspended ‘Fluvax\/Afluria’ after the deluge of adverse reports from Australia: <\/strong> In a closed door meeting conducted by the CDC in 2000<\/a>, doctors alluded to their concerns over heavy metal toxicity in vaccines; while acknowledging a glaring void in scientific research on this neglected aspect of synergy,<\/strong><\/p>\n In the same breath Johnson also stressed the necessity of using aluminum as an adjuvant (immune stimulant) in vaccines,<\/strong><\/p>\n \u201cAluminum salts are important in the formulatin<\/strong><\/p>\n In 1927, Dr. Victor Vaughn, a toxicologist with the University of Michigan, testified before the Federal Trade Commission that \u201call salts of aluminum are poisonous when injected subcutaneously or intravenously\u201d. According to the American Academy of Pediatrics, \u201cAluminum 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.\u201d Neil Miller <\/a><\/strong><\/p>\n Aluminum is a highly conductive ‘<\/strong>electropositive’ <\/strong>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 \u201cconductivity\u201d; in particular the brain which consists primarily of neurons.<\/strong><\/p>\n \u2018Under a microscope a neuron looks like an octopus with many tentacles<\/a>. A neuron can transmit an electrical impulse to the next neuron. The network of electrical impulses enables us to receive information from the physical world and then send it to our brains, and vice versa. Without the neuron circuits our bodies would completely shut down, like turning off the power supply to a city. If it were possible to describe the nervous system as a circuit diagram, with each neuron represented by a single pinhead, such a circuit diagram would require an area of several square kilometres it would be several hundred times more complex than the entire global telephone network.\u2019<\/strong><\/p>\n As Dr. Gary Tunsky<\/a> 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.<\/strong><\/p>\n \u201cYour 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) \u2013 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\u2019s 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\u2019s where the blockages are occurring, the brain, the spine, (the intestines\/bowel) fingers & toes \u2013 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. \u201d Dr. Gary Tunsky<\/strong><\/p>\n 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 \u201cstagnant\u201d blood), is comparable to the black paste-like build-up found over time in the lining of your drains \u2013 especially in terms of its impact on your vital health. <\/strong><\/p>\n Currently children are getting 17 shots containing aluminum, a quadrupling of the amount given since the 1970\u2019s. It is found in Hepatitis A, Hepatitis B, DTaP (diphtheria, tetanus, pertussis), MMR, Hib, Pneumococcal & Gardasil (HPV) vaccines.<\/strong><\/p>\n Based on Dr. David Ayoub\u2019s findings<\/a> children, on average, receive 2-400 micrograms per vaccine, over a milligram of Aluminum; a concentration & dosage that is 10 \u2013 20 times more toxic than Mercury. Multiple vaccines are far worse, over a 1000 micrograms on average for a triple set shot. <\/strong><\/p>\n 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. <\/span><\/strong><\/p>\n Acute exposure to heavy metals can lead to a host of auto-immune disorders: <\/strong>Downs Syndrome, Autism, Schizophrenia, ALS, Lupus, Parkinson\u2019s & Alzheimer\u2019s Disease, cognitive disfunction<\/a>.<\/strong><\/p>\n \u2018Research 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 \u2013 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 \u2013 50 times higher than safety levels.\u2019 Food & Drug Administration Report<\/strong><\/p>\n \u2018The results for aluminum were almost identical to ethyl mercury (Thimerosal) because the amount of aluminum in vaccines goes almost exactly with the mercury.\u2019 Dr. Tom Verstraeten\/Epidemiologist The trivalent influenza vaccine contains 3 sets of either \u2018killed\u2019 or \u2018heat-treated DNA\/RNA strands, ostensibly a safe variant blueprint of the live virus itself. Adjuvants are designed to jump-start or supercharge the immune system \u2013 to induce a robust immune response; thus immunizing the body against the likelihood of succumbing to the flu while avoiding the direct spread of infection. In truth no virus is fully killed during the vaccine manufacturing process. Typically the vaccinee is left more susceptible to catching the seasonal flu (twice a likely to catch swine flu<\/a>). Depending on the degree of compromised immune system &\/or pre-existing medical condition involved, a vaccine induced Cytokine Storm can rapidly trigger complete auto-immune failure throughout the individual\u2019s body. <\/strong><\/p>\n The primary contributors to the cytokine storm are TNF-a (Tumor Necrosis Factor-alpha) and IL-6 (Interleukin-6). The cytokine storm is an inappropriate (exaggerated) immune response that is caused by rapidly proliferating and highly activated T-cells or natural killer (NK) cells. These cells are themselves activated by infected macrophages. The cytokine storm must be treated and suppressed or lethality can result.\u2019 \u2018The flu virus causes immune cells to produce cytokine molecules that increase inflammation. Normally this is controlled, but in extreme cases, a \u201ccytokine storm\u201d occurs. This can cause tissue and organ damage, and even death. When you\u2019re fighting the flu, you feel bad not because of the virus but rather because of the \u201ccytokine storm.\u201d But get this: All vaccines trigger their own cytokine storms. And researchers now know that increased inflammation is at the heart of most illness and disease. Which means the vaccines themselves are hazardous to your health. The solution is to avoid flu shots, and if you\u2019ve had them in the past, to take nutrients that will strengthen your immune system and reduce inflammatory cytokine activity.\u2019 Dr. Russell Blaylock NOTE: an overabundance of T-Cells, Microphages & oxygen free radicals flood the body \u2013 attacking the lungs, kidneys, liver, brain, impeding Endocrine, Lymphatic, Immune & Nervous system function. <\/strong><\/p>\n 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\u2019 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. <\/strong> <\/strong><\/p>\n \u201cWe hope that the new recommendations promulgated by the Advisory Committee on Immunization Practices (ACIP) will help. Rather than focus on \u201chigh-risk groups,\u201d as has been done in the past, the ACIP now recommends annual influenza vaccination for everyone 6 months of age or older.\u201d \u2018Influenza vaccine (seasonal). (Minimum age: 6 months for trivalent inactivated influenza vaccine [TIV]; 2 years for live, attenuated influenza vaccine [LAIV]) \u2022 Administer annually to children aged 6 months through 18 years.\u2019 CDC Standard Immunization Schedule age 0-6 yrs
\nhttp:\/\/www.theglobeandmail.com\/news\/technology\/science\/study-prompts-provinces-to-rethink-flu-plan\/article1303330\/<\/a><\/strong> <\/strong><\/p>\n
\nhttp:\/\/www.plosmedicine.org\/article\/info%3Adoi%2F10.1371%2Fjournal.pmed.1000258<\/a><\/strong><\/p>\n
\nhttp:\/\/theweek.com\/article\/index\/211910\/a-flu-vaccine-that-lasts-forever<\/a><\/strong><\/p>\n![\"influenza_virus_600\"](\"http:\/\/vaccineresistancemovement.org\/wp-content\/uploads\/2011\/01\/influenza_virus_6001.jpg\" "\\"influenza_virus_600\\"")
\u2018Production of viral vaccines generally involves inoculation of a cell substrate with a vaccine seed and purification of bulk product from these cells after a sufficient time for replication of the virus or production of vaccine proteins. Other raw materials (e.g., tissue culture reagents, stabilizers) may be added to the product at various stages of production. Thus, adventitious agents could theoretically enter a viral vaccine through any of these ingredients. <\/a><\/strong><\/div>\nClose control of the vaccine manufacturing environment (by producing vaccines in sophisticated modern facilities), appropriate testing of the raw materials, and testing of both the bulk and final products can help ensure that adventitious agents have not entered the vaccine. Most vaccines are subjected to inactivation or purification steps that can reduce likelihood of contamination with adventitious agents <\/strong>(<\/span><\/span><\/span><\/span><\/span><\/span>mutability factor\/cross-contamination)<\/span><\/span><\/span><\/span><\/span><\/span><\/strong><\/a>.<\/a>\u2019 US Centers for Disease Control<\/strong><\/div>\n<\/div>\n![\"\"](\"http:\/\/vaccineresistancemovement.org\/wp-content\/uploads\/2011\/01\/cdc-logo-world_medium.jpg\" "\\"cdc-logo-world_medium\\""){kind=logo}
<\/a><\/div>\n\u201cMany novel vaccines are produced in animal cell substrates, and emerging infectious diseases may theoretically be transmitted from animals to humans through these vaccines. The challenge of identifying potential adventitious agents in vaccines closely parallels the challenge of identifying the agents causing particular emerging infectious diseases.\u2019 CDC<\/strong><\/span><\/div>\n
\n<\/strong><\/span><\/div>\n![\"cv12\"](\"http:\/\/vaccineresistancemovement.org\/wp-content\/uploads\/2011\/01\/cv123.jpg\" "\\"cv12\\"")
\u2018The experience in the early 1960s with SV40 contamination of poliovirus and adenovirus vaccines and the continuing questions regarding whether SV40 could be responsible for some human neoplasms (types of cancer) underscore the importance of keeping viral vaccines free of adventitious agents. This is particularly important when there is a theoretical potential for contamination of a vaccine with viruses that might be associated with neoplasia (cancer).<\/strong> <\/strong> <\/strong><\/div>\nIt is unclear whether neoplastic cells have a greater or lower adventitious agent risk than other types of cells. Because they can be grown for long periods in tissue culture, there may be greater opportunities for any adventitious agents to be detected. Because neoplastic cells survive indefinitely, it is easier to qualify and bank cells that have passed all tests, especially as compared with primary cells (which are derived repeatedly from live tissue and must be re-qualified with each use). Moreover, many neoplastic cells can be grown in serum-free medium, potentially reducing the likelihood of contamination with bovine adventitious agents. <\/strong><\/div>\n\n![\"neoplastic](\"http:\/\/vaccineresistancemovement.org\/wp-content\/uploads\/2011\/01\/neoplastic-cells.jpg\" "\\"neoplastic")
However, if their growth in tissue culture is not well controlled, there may exist additional opportunities for contamination of cells with a longer lifespan. In cases of neoplastic cells for which the transforming event is unknown, there is also a theoretical possibility that transformation occurred as a result of a previous viral infection. Because some mammalian tumors and some cells transformed by viruses contain infectious virus, cells transformed by an unknown mechanism have a theoretical risk of containing transforming virus. <\/strong><\/p>\n
\nhttp:\/\/www.fda.gov\/ohrms\/dockets\/ac\/01\/briefing\/3750b1_01.htm<\/a><\/strong><\/p>\n
\nhttp:\/\/winningcancer.com\/index.php\/2010\/03\/heavy-metals-mercury-and-cancer\/#arrive<\/a><\/strong><\/p>\n<\/div>\n
\nhttp:\/\/mercury-freedrugs.org\/docs\/100915_CoMeD_PR_OnOIG_HHS_fnldb.pdf<\/a><\/strong><\/p>\n![\"Panvax\"](\"http:\/\/vaccineresistancemovement.org\/wp-content\/uploads\/2011\/01\/Panvax.jpg\" "\\"Panvax\\"")
Most multi-dose vaccines currently average 25 micrograms of Thimerosal Mercury. Based on EPA standards this is considered a safe level of exposure for a 2500 pound adult. Australia\u2019s 2010-11 Flu vaccine Panvax contains 50 micrograms of Thimerosal; technically a safe level of exposure for a 1100 pound adult. Unless you were born a Mack Truck this is tantamount to attempted murder. <\/strong>Time for the Australian community to rise up against this tyranny with a massive Class Action law suit.<\/strong><\/p>\n
\nhttp:\/\/contribute.abc.net.au\/_Panvax\/blog\/718273\/32422.html<\/a><\/strong><\/p>\n
\nhttp:\/\/www.newsinferno.com\/archives\/19877<\/a><\/strong><\/p>\n
\nhttp:\/\/secure.healthlinks.net.au\/content\/csl\/pi.cfm?product=csppanva11209<\/a>
\nhttp:\/\/preventdisease.com\/news\/pdf\/CSL_PANVAX_H1N1_SEPT2009.pdf<\/a><\/strong><\/p>\n
\nhttp:\/\/www.abc.net.au\/news\/stories\/2010\/04\/22\/2880521.htm?site=news<\/a><\/strong><\/p>\n\n
\nhttp:\/\/www.abc.net.au\/news\/stories\/2010\/04\/29\/2885884.htm?site=news<\/a><\/strong><\/p>\n![\"Afluria\"](\"http:\/\/vaccineresistancemovement.org\/wp-content\/uploads\/2011\/01\/Afluria.jpg\" "\\"Afluria\\"")
The United States flu vaccine for 2010-2011\/Afluria\u00ae was manufactured by CSL Laboratories in partnership with Merck Pharmaceuticals. Ingredients: 24.5 mcg of thimerosal mercury (safe level for a 2450 pound adult), Neomycin & Polymyxin (antibiotics associated with Kidney Failure, hazardous to fetus), 3 strains of flu virus including A\/Brisbane\/59\/2007 (H1N1 subunits)<\/strong><\/p>\n
\nhttp:\/\/www.merck.com\/product\/usa\/pi_circulars\/a\/afluria\/afluria_pi.pdf<\/a><\/strong><\/p>\n
\nhttp:\/\/preventdisease.com\/news\/pdf\/CSL_2009_LatestAfluriaPackageInsert_ucm112730.pdf<\/a><\/strong><\/p>\n![\"Fluviral\"](\"http:\/\/vaccineresistancemovement.org\/wp-content\/uploads\/2011\/01\/Fluviral.jpg\" "\\"Fluviral\\"")
Canadian health practitioners should soon expect a flood of adverse reactions to this year\u2019s flu shot \u2018Fluviral\u2019. Not only does this GSK produced vaccine contain twice the Industry standard for Thimerosal considered to be at an \u201cacceptable\u201d level, formaldehyde, multiple toxic buffers & detergent; but with addition of H1N1 sub-units, and based on the 2009 BCCDC report implicating the flu shot itself in doubling one\u2019s susceptibility to catching Swine Flu<\/a>, the odds are we will soon see a cavalcade of vaccine induced trauma, especially in infants & pregnant women. <\/strong><\/p>\n
\n15 \u03bcg HA \u2013 A\/California\/7\/2009 (H1N1)-like strain (A\/California\/7\/2009 NYMC X-179A),
\n15 \u03bcg HA \u2013 A\/Perth\/16\/2009 (H3N2)-like strain (A\/Victoria\/210\/2009 NYMC X-187),
\n15 \u03bcg HA \u2013 B\/Brisbane\/60\/2008-like strain (B\/Brisbane\/60\/2008).<\/strong><\/p>\n
\nhttp:\/\/www.gsk.ca\/english\/docs-pdf\/Fluviral_2010.pdf<\/a><\/strong><\/p>\n
\nhttp:\/\/www.dailymail.co.uk\/health\/article-1342933\/Flu-jab-given-fives.html#ixzz1BLr14j19<\/a><\/strong><\/p>\n
\n‘Doctors should stock alternative vaccines for under fives who are due to have the seasonal flu vaccine this winter, a letter from the head of immunisation at the Department of Health has said. The action is being taken as rate of convulsions caused by high fever among children in Australia given the jab was ten times higher than normal. Up to one in 100 children given the jab, made in Australia by CSL and marketed in the UK by Pfizer, suffered febrile convulsions in the following hours and days. ‘
\nhttp:\/\/www.telegraph.co.uk\/health\/healthnews\/7918351\/Flu-jab-linked-to-fits-in-under-fives-officials.html<\/a><\/strong><\/p>\n![\"toxic\"](\"http:\/\/vaccineresistancemovement.org\/wp-content\/uploads\/2011\/01\/toxic.jpg\" "\\"toxic\\"")
\u201cAluminum & 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.\u201d Dr. Johnston
\n<\/strong><\/p>\n
\nhttp:\/\/www.vacinfo.org\/Aluminum%20in%20Vaccines,%20Free%20ebook.pdf<\/a><\/strong><\/p>\n![\"necrotizing_bronchiolitis_1\"](\"http:\/\/vaccineresistancemovement.org\/wp-content\/uploads\/2011\/01\/necrotizing_bronchiolitis_1.jpg\" "\\"necrotizing_bronchiolitis_1\\"")
\u2018A cytokine storm is the systemic expression of a healthy and vigorous immune system resulting in the release of more than 150 inflammatory mediators (cytokines, oxygen free radicals, and coagulation factors). Both pro-inflammatory cytokines (such as Tumor Necrosis Factor-alpha, InterLeukin-1 & InterLeukin-6) and anti-inflammatory cytokines (such as interleukin 10, and interleukin 1 receptor antagonist) are elevated in the serum, and the fierce and often lethal interplay of these cytokines is referred to as a \u201cCytokine Storm\u201d. <\/strong><\/p>\n
\nhttp:\/\/www.cytokinestorm.com\/<\/a><\/strong><\/p>\n
\nhttp:\/\/w3.newsmax.com\/blaylock\/62b.cfm<\/a><\/strong><\/p>\n![\"Viral](\"http:\/\/vaccineresistancemovement.org\/wp-content\/uploads\/2011\/01\/Viral-pneumonia1.jpg\" "\\"Viral")
Manifestations of a vaccine triggered Cytokine Storm can range from high fever & extreme vomiting to Bronchitis, Hemorrhagic fever (drowning of lungs with fluid), Anaphylaxis (severe allergic reaction), Guillain\u2013Barr\u00e9 syndrome (form of paralysis), Encephalitis (brain inflammation), acute respiratory distress syndrome, Sepsis, Bacterial Pneumonia, febrile convulsions, Sub-Clinical Epileptic Seizures, Grand Mal Epileptic Seizures, Narcolepsy, organ failure, blindness, coma & death.<\/strong><\/p>\n
\nhttp:\/\/www.nejm.org\/doi\/full\/10.1056\/NEJMp1012333<\/a><\/strong> <\/strong><\/p>\n