“There 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.” J. Anthony Morris, Former Chief  Vaccine Control Officer, FDA

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.

‘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.’ The Cochrane Review 

‘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’ found on safety of inactivated vaccines in young children.’ The Cochrane Review 

‘A “perplexing” Canadian study linking H1N1 to seasonal flu shots is throwing national influenza plans into disarray and testing public faith in gov’t agencies responsible for protecting the nation’s health. Study confounds infectious-disease experts in suggesting that people vaccinated against seasonal flu are twice as likely to catch swine flu. “It has confused things very badly,” said Dr. Ethan Rubinstein, head of adult infectious diseases at the University of Manitoba. “And 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.”’
http://www.theglobeandmail.com/news/technology/science/study-prompts-provinces-to-rethink-flu-plan/article1303330/

‘Association between the 2008–09 Seasonal Influenza Vaccine and Pandemic H1N1 Illness during Spring–Summer 2009: Four Observational Studies from Canada: ‘Estimates 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 2008–09 TIV (trivalent inactivated influenza vaccine aka regular flu shot) was associated with increased risk of medically attended pH1N1 illness during spring–summer 2009′
http://www.plosmedicine.org/article/info%3Adoi%2F10.1371%2Fjournal.pmed.1000258

“Because the influenza virus genome is segmented, coinfection of a single host cell with two or more different influenza viruses can result in a reassortment (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.” Dr. Antony Fauci, director of the National Institute of Allergy & Infectious Diseases (co-patent holder of “IImmunologic enhancement with intermittent interleukin-2 therapy” described as being central to gene therapies and the future of “geneto-pharmaceuticals”)

Universal Flu Vaccine will unleash a new cats cradle of mutagenic viruses; which in turn will spawn a new wave of counter shots. – ‘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.”‘
http://theweek.com/article/index/211910/a-flu-vaccine-that-lasts-forever

“Injecting mercury into pregnant women and children is absurd. Examine studies which suggest otherwise, and you will find the funding for the study came from those who directly or indirectly profit from, or fear liability from, the use of mercury-containing vaccines.”
http://mercury-freedrugs.org/docs/100915_CoMeD_PR_OnOIG_HHS_fnldb.pdf

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’s 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. Time for the Australian community to rise up against this tyranny with a massive Class Action law suit.

‘Included 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 “first tier” 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 “reasonably expected to be a human carcinogen” (International Agency for Research on Cancer – IARC, 1999). Βeta-Propiolactone is a disinfectant. Panvax is formulated using chick embryos (Ovalbumin). People who suffer allergy to eggs or anaphylactic reactions may experience problems.’
http://contribute.abc.net.au/_Panvax/blog/718273/32422.html

‘The 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.’
http://www.newsinferno.com/archives/19877

Panvax: Package insert –
http://secure.healthlinks.net.au/content/csl/pi.cfm?product=csppanva11209
http://preventdisease.com/news/pdf/CSL_PANVAX_H1N1_SEPT2009.pdf

Early vaccine trauma report from Australia (high temperatures & febrile convulsions) – 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.”If it’s longer than 12 hours ago then there is no risk. But if it’s 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.”
http://www.abc.net.au/news/stories/2010/04/22/2880521.htm?site=news

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.

• The attack often begins with the child losing consciousness, and shortly afterwards the body, legs and arms go stiff.
• The head is thrown backwards and the legs and arms begins to jerk.
• The skin goes pale and may even turn blue briefly.
• The attack ends after a few minutes and the shaking stops. The child goes limp, and then normal colour and consciousness slowly return.
• Some children regain consciousness faster than others.

Australian vaccine scandal worsening – 250 reports of adverse reactions – a figure experts and parents fear is being severely underestimated. It has became a hot topic in online parenting forums such as ‘Essential Baby’, where hundreds of mothers and fathers have expressed their fears and detailed nightmare stories of their children’s reactions.

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. “I grabbed him out of the bath and then he started shaking uncontrollably. He couldn’t stand or hold anything, he was shaking that much. “He curled his arms over his chest, kept gagging and letting out squeals. I had no idea what the hell was going on.”
http://www.abc.net.au/news/stories/2010/04/29/2885884.htm?site=news

The United States flu vaccine for 2010-2011/Afluria® 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)

Afluria (produced by Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.): Package Insert – 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.

Administration of CSL’s 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-Barré 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.
http://www.merck.com/product/usa/pi_circulars/a/afluria/afluria_pi.pdf

Afluria® – Package Insert
http://preventdisease.com/news/pdf/CSL_2009_LatestAfluriaPackageInsert_ucm112730.pdf

Canadian health practitioners should soon expect a flood of adverse reactions to this year’s flu shot ‘Fluviral’. Not only does this GSK produced vaccine contain twice the Industry standard for Thimerosal considered to be at an “acceptable” 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’s susceptibility to catching Swine Flu, the odds are we will soon see a cavalcade of vaccine induced trauma, especially in infants & pregnant women.

The main target group for this shot encompasses 6 months through ≥65 years of age. Anyone to speak of with 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.

‘Fluviral’ (Manufactured for Canada): Analysis of ingredients –

Multiple viruses (heat-treated/total of 45 micrograms) including 2009’s H1N1 sub-units –
15 μg HA – A/California/7/2009 (H1N1)-like strain (A/California/7/2009 NYMC X-179A),
15 μg HA – A/Perth/16/2009 (H3N2)-like strain (A/Victoria/210/2009 NYMC X-187),
15 μg HA – B/Brisbane/60/2008-like strain (B/Brisbane/60/2008).

Thimerosal (100μg/mL) –  50 micrograms of Thimerosal mercury per shot (0.5 microgram/ 0.5 mL dose  x 100μg/mL). Based on EPA standards this constitutes a safe level for a 1100 pound adult.

Formaldehyde – used as “a preservative & disinfectant”, binds to the proteins in your DNA, known to cause cancer, chronic bronchitis, eye irritation when exposed to the body’s immune system.

Potassium Chloride – Used as part of a phosphate buffered saline in the shot. The majority of the potassium chloride produced is used for making fertilizer, since the growth of many plants is limited by their potassium intake. As a chemical feedstock it is used for the manufacture of potassium hydroxide and potassium metal; and as a flux for the gas welding of aluminium. Hyperkalemia. May induce Cardiac arrest (especially in renal impairment or if administered too rapidly). May cause pain and thrombophlebitis if administered in high concentration into small veins in patients with cardiac disease, renal impairment, or acidosis:  monitoring of acid-base balance, potassium levels, and ECG is recommended. Potassium chloride is also used as the third of a three-drug combination in lethal injection. Additionally, KCl (AN aqueous solution form of Potassium Chloride) is used, albeit rarely, in fetal intracardiac injections in second- and third-trimester induced abortions.

Sodium Phosphate Dibasic Heptahydrate & Potassium Phosphate Monobasic: Both excipients (pharmacologically inactive substances, carriers for the active ingredients of a medication)) used as part of a phosphate buffered saline in the shot. May sequester calcium and cause calcium phosphate deposits in kidneys. Chronic ingestion or inhalation may induce systemic phosphorous poisoning. Liver damage, kidney damage, jaw/tooth abnormalities, blood disorders & cardiovascular effects can result. Phosphates are slowly and incompletely absorbed when ingested, and seldom result in systemic effects. Such effects, however, have occurred. Symptoms may include vomiting, lethargy, diarrhea, blood chemistry effects, heart disturbances, nausea, vomiting, stomach/abdominal pain or bloating, dizziness, or headache and central nervous system effects. The toxicity of phosphates is because of their ability to sequester calcium.

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

Sodium Deoxycholate: A detergent added to new generation of ‘Split Vaccines’ to modify the whole virus which causes cell death and symptoms such as burning, redness, and swelling. It has been shown to weaken the blood-brain-barrier (BBB) and subsequently activate seizures.  It demonstrates synergistic toxicity — notably with Amphotericin B, the antifungal listed above. Recommended for stripping endotoxin (Lipopolysaccharide or LPS) from immobilized Polymyxin B columns; for use with the the Thermo Scientific Detoxi-Gel Endotoxin Removing Gel. The effectiveness of a detergent in any application is dependent on the detergents concentration. Too much or too little detergent can often have a deleterious effect.

Fluviral® (2010-2011) Package Insert
http://www.gsk.ca/english/docs-pdf/Fluviral_2010.pdf

UK Gov’t reluctantly bans 2010-11 Flu vaccine for ‘under-fives’: ‘Ministers and senior Government advisers last night ruled that the immunisation programme for those aged six months to five years – which was quietly cancelled earlier this year – would not have significant ‘gain’. The decision came after the Government’s 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.
http://www.dailymail.co.uk/health/article-1342933/Flu-jab-given-fives.html#ixzz1BLr14j19

Britain had already suspended ‘Fluvax/Afluria’ after the deluge of adverse reports from Australia:
‘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. ‘
http://www.telegraph.co.uk/health/healthnews/7918351/Flu-jab-linked-to-fits-in-under-fives-officials.html

In a closed door meeting conducted by the CDC in 2000, 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,

“Aluminum & mercury are often simultaneously administered to infants, both at the same site & at different sites. However, there is absolutely no data, including animal data, about the potential for SYNERGY, additively or antagonism, all of which can occur in binary metal mixtures that relate and allow us to draw any conclusions from the simultaneous exposure to these two salts in vaccines.” Dr. Johnston

In the same breath Johnson also stressed the necessity of using aluminum as an adjuvant (immune stimulant) in vaccines,

“Aluminum salts are important in the formulatin

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.

‘Under a microscope a neuron looks like an octopus with many tentacles. 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.’

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 Myelin Sheath, neurons, the meninges/spine, cardiac cells, breasts & ovaries (in women), prostate (in men). Blood is made of water. When you stick aluminum in your blood, anything that’s toxic debris is going to bond to and coagulate and cause a congestive coccidiosis and this stuff gets caught in the tiny highways & byways. So you have the big gushing arteries & veins but they byfricate and branch into streams like a river; and they branch in again to the tiny arterial & capillary bits. That’s where the blockages are occurring, the brain, the spine, (the intestines/bowel) fingers & toes – which turn blue, choking of the micro-vessels from all the sludge that gets caught from all these repetitive hits/vaccinations, over & over. There are 60,000 miles of blood-vessels in one body.They run through every part of your muscle, your bone, your brain. Anywhere you stick an inter-muscular injection it goes into the blood. ” Dr. Gary Tunsky

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.

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.

Acute exposure to heavy metals can lead to a host of auto-immune disorders: Downs Syndrome, Autism, Schizophrenia, ALS, Lupus, Parkinson’s & Alzheimer’s Disease, cognitive disfunction.

‘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 Report

‘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

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

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

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

‘The flu virus causes immune cells to produce cytokine molecules that increase inflammation. Normally this is controlled, but in extreme cases, a “cytokine storm” occurs. This can cause tissue and organ damage, and even death. When you’re fighting the flu, you feel bad not because of the virus but rather because of the “cytokine storm.” 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’ve had them in the past, to take nutrients that will strengthen your immune system and reduce inflammatory cytokine activity.’ Dr. Russell Blaylock
http://w3.newsmax.com/blaylock/62b.cfm

Manifestations of a vaccine triggered Cytokine Storm can range from high fever & extreme vomiting to Bronchitis, Hemorrhagic fever (drowning of lungs with fluid), Anaphylaxis (severe allergic reaction), Guillain–Barré syndrome (form of paralysis), Encephalitis (brain inflammation), acute respiratory distress syndrome, Sepsis, Bacterial Pneumonia, febrile convulsions, Sub-Clinical Epileptic Seizures, Grand Mal Epileptic Seizures, Narcolepsy, organ failure, blindness, coma & death.

NOTE: an overabundance of T-Cells, Microphages & oxygen free radicals flood the body – attacking the lungs, kidneys, liver, brain, impeding Endocrine, Lymphatic, Immune & Nervous system function.

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.”
http://www.nejm.org/doi/full/10.1056/NEJMp1012333

‘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
http://www.cdc.gov/vaccines/recs/schedules/downloads/child/2010/10_0-6yrs-schedule-pr.pdf

GlaxoSmithKline quietly re-introduces Thimerosal into UK Flu Vaccine ‘Pandemrix’: ‘Up to a million under-fives have been inoculated against the flu virus with a controversial vaccine containing poisonous mercury. Pandemrix has been given to almost a quarter of all healthy babies and young children as well as thousands of older children with health problems. Inquiries by the Sunday Express reveal it contains a preservative made with a form of mercury that was phased out of childhood vaccines in 2004 after fears about its safety.’
http://www.express.co.uk/posts/view/222000/Child-flu-vaccine-contains-mercuryChild-flu-vaccine-contains-mercury#ixzz1BJQXjZbL

“Thimerosal plays an important role in preventing bacterial contamination. Regulators across the world have concluded there is no evidence the level of thimerosal in vaccines poses a health risk.” GlaxoSmithKline

“Extensive studies have failed to find any evidence that these low levels of Thimerosal carry any risk of neurotoxicity.” UK Medicines & Healthcare Products Regulatory Agency

It should come as no surprise that the flagship model, the first major Cloned cell-based vaccine ever for mass production, will be introduced in the Fall of 2011 in the United States with the annual Flu shot; touted as a ‘Recombinant Trivalent Hemagglutinin Protein-based Influenza Vaccine‘.

Novartis Vaccines & Diagnostics has been awarded a $487 million contract by the US Dep’t of Health & Human Services, a joint venture totaling nearly $1 billion US in investment, to produce ‘50 million doses of seasonal trivalent flu vaccine, and up to 150m doses of monovalent vaccine‘ in preparation for a potential Pandemic.

World Health Organization chief addresses growing problem of vaccine ‘mistrust’ among population: “In some cases, persuading the public to seek vaccination has become even more problematic than during the pandemic…the problem of public mistrust extends well beyond influenza vaccines.  We may need to accept the fact that public perceptions about vaccine safety can be permanently changed by unfounded fears, to an extent that no amount of evidence can change the public’s mind. This is a worrisome new trend that needs to be addressed.” Margaret Chan/Director-General, WHO
http://www.who.int/dg/speeches/2011/eb_20110117/en/index.html

UK Gov’t using threat of artificial scarcity & “healthy” segment of population to encourage greater vaccine uptake: ‘The “worried well” should be banned from paying for the flu jab privately at pharmacies, according to a leading doctor, as chemists begin to run out of the vaccine.

Healthy people buying the flu jab have compounded shortages in the NHS and left those at greatest risk struggling to get the vaccine, claimed Dr Clare Gerada, the chairman of the Royal College of GPs. Pharmacies and GPs are reporting that they have run out as thousands seek protection from the worst winter flu outbreak in a decade.’

The Placenta, & breast milk (Colostrum) are inextricably linked, providing a baby’s primary initial source of nourishment through the long journey of formation in utero; while supplying the basic building blocks of life necessary to guarantee a safe transition into early childhood development. Mother & baby share the same Immune system while the baby is ‘in Utero’. It seems almost inconceivable given the scientific literature in circulation, but somehow the CDC, WHO & local health authorities in countries around the world have begun recommending all pregnant women & babies as young as 6 months receive Influenza vaccine during first trimester.

‘The Flu Shot is Safe for Pregnant Women – Flu shots are a safe way to protect the mother and her unborn child from serious illness and complications of flu. The flu shot has been given to millions of pregnant women over many years. Flu shots have not been shown to cause harm to pregnant women or their babies. It is very important for pregnant women to get the flu shot.’ CDC
http://www.cdc.gov/flu/protect/vaccine/pregnant.htm

‘A shocking report from the National Coalition of Organized Women (NCOW) presented data from two different sources demonstrating that the 2009/10 H1N1 vaccines contributed to an estimated 1,588 miscarriages and stillbirths – as high as 3,587 cases. Studies conducted by the CDC have been shown to miss from 10% to 90% of the actual cases because of under-reporting.’

‘Studies of the organs and tissues of the first generation progeny revealed mercury in the stomach and intestine at birth and in the first week of life, apparently on account of the entry of mercury through the placental barrier and by way of their mother’s milk. Subsequently, it was noted that the first-generation progeny of mothers that had been previously exposed to the ethyl mercury compound had significantly reduced fertility in comparison to controls. The second generation progeny had low viability, lagged in their weight growth, and were retarded with respect to ossification in several cases. Finally, it was then observed when mating the second generation progeny that there was a significant decrease in fertility in comparison to the control group.’

‘70% of pregnant women in UK refusing Influenza shot: ‘Almost three-quarters of Britain’s pregnant women have still not received the flu jab this winter, according to Andrew Lansley, the health secretary. In a letter to his Labour shadow, John Healey, Lansley said that although the number of expectant mothers who have received the seasonal flu injection had almost doubled this year, more than 70% remain unvaccinated.’
http://www.guardian.co.uk/society/2011/jan/15/pregnant-women-flu-jab-lansley

‘The government has been forced to release stocks of last winter’s swine flu vaccine to bolster this year’s supplies of the seasonal flu jab. While ministers have insisted there should be enough across England, they have acknowledged a “mismatch”, with some regions having too much vaccine and others suffering a shortage.
http://www.guardian.co.uk/society/2011/jan/20/flu-related-deaths-uk

‎‘Influenza A H1N1 (2009) ‘swine’ flu and Influenza B remain the predominant strains circulating although sporadic cases of H3N2 have also been seen. In the past week, the HPA has been notified of a further 11 people who have died with confirmed flu, bringing the total number since the flu season began in October this year to 50. 45 of these people died with the H1N1 (2009) strain and five with Influenza B.’

Note: ‘Study confounds infectious-disease experts in suggesting that people vaccinated against seasonal flu are twice as likely to catch swine flu.’

Concern over mounting “general scepticism” amongst population: “There is undoubtedly pandemic fatigue reflecting the massively overhyped preparation last year. The fact that such efforts went into entirely valueless treatments last year (Tamiflu) has only compounded the general scepticism.”
http://www.guardian.co.uk/society/2011/jan/10/pregnant-women-flu-jabs-midwives

On October 16th, 2009 the Council on Foreign Relations, a powerful Globalist think tank met in New York to discuss policy advisement measures on the Government’s H1N1 program. The minutes of the symposium reveal various techniques employed behind the scenes to influence the ‘herd’; including using artificial scarcity to increase demand, blatant fear mongering & counter measures to quell the “anti-vaccine movement”. The program was clearly in disarray.

“I think what would work better would be to say that there was a shortage and people tend to buy more of something that’s in demand (laughter). We saw that— there was one season where, really, people lined up all night to get a flu shot (more laughter).” Lone Simonsen, Research Director at the Dep’t of Global Health, George Washington University

“I think we’re all aware the anti vaccine movement is having a field-day on the internet and on media outlets like Fox News (chuckle heard) causing reductions in vaccine uptake and it appears to be a pretty unholy alliance of the ultra right & ultra left working together in a sort of Hitler-Stalin pact (hysterical laughter). I’m not sure we’re countering these people very well. And you have to take these people on in a different style than scientists are used to. We have to develop better sound bytes. You have to develop better discussion. You can’t really debate these people but you have to develop better counter methods.”

Dr Gerada said that allowing those who could afford it to buy the jab had upset the “delicate balance” of availability and contributed to shortages, leading to general concern about who should and should not have the vaccine.
http://www.telegraph.co.uk/health/flu/8250231/Worried-well-should-be-banned-from-having-flu-jab-says-leading-GP.html

“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

The vanguard in the field of vaccine research claim “Cell-based vaccine production dramatically reduces the possibility for contamination”. No matter which route you take in terms of the application of 21st century vaccine production technology (cloning), all roads will inevitably lead to cancer. The CDC & NIAID openly admit to a “theoretical” risk of viral cross contamination, the presence of ‘endogenous retroviruses‘ (remnants of ancestral exogenous retroviral infections fixed in the germline DNA), ‘adventitious agents‘ (mutagenic viral strains) & ‘oncogenic agents’ (neoplasms or cancer), when harnessing (multiple) viruses in combination with heavy metals, tissue culture reagents, & stabilizer cocktails for vaccines.

Let us review some of the noteworthy findings of National Health Regulators & Medical Practitioners/Researchers thus far:

1. ‘Because the influenza virus genome is segmented, coinfection of a single host cell with two or more different influenza viruses can result in a reassortment (or shuffle) of their genetic material.’

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

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

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

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

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

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

8. ‘The human body retains a genetic memory of the foreign substances (endogenous retroviruses – remnants of ancestral exogenous retroviral infections fixed in the germline DNA) to which it has been exposed, including viral and bacterial vaccines…There appears to be a limit on how much foreign material to which the human body can be exposed before some level of genetic damage occurs and a chronic disease initiates.‘ Testimony of Dr. Howard B. Urnovitz, August 3, 1999, Committee on Government Reform and Oversight/House of Representatives

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

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

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

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

Note: Over 200 influenza viruses are circulating each year. Nature is highly unpredictable; it cannot be isolated in this respect. During the winter months the T Lymphocytes in your lungs (white blood cells vital to natural immunity) are starved of Vitamin D3 (steroid hormone derived from sunlight); thus have difficulty processing Vitamins C & E. A Universal Flu Vaccine, in addition to disengaging the T Lymphocytes in your lungs, will unleash a new cats cradle of mutagenic viruses; which in turn will spawn another wave of counter shots. Excipients such as Thimerosal, toxic detergents & antibiotics, further undermine the body’s ability to fight off infection by neutralizing Thyroid function (a process vital to regulating your overall metabolism – limits over-abundance of free radicals with anti-oxidants).

As a safe alternative to the flu shot, take Liquid Vitamin D3 (5-10,000 IU/per day); in addition to Wild Salmon/Krill Oil (source of Vitamin D3 & Omega 3 fatty acids), organic oranges (or high quality Vitamin C supplement), Kale & Cilantro (chelates heavy metal toxicity – loaded with anti-oxidants), organic Apple Cider Vinegar (one shot semi-daily – helps maintain the proper alkaline over acidic levels in the body) plus a teaspoon of Sodium Bicarbonate (organic Baking Soda – cancer fighter), taken semi-regularly. This regime should be balanced with a healthy reduction/elimination of the following: gluten, casein, sugars, iodized salts, poly-saturated fats, all genetically modified food/produce/liquids.

See VRM: 5 Reasons Not To Get The Flu Shot http://vaccineresistancemovement.org/?p=12642

See VRM: The Flu Report http://vaccineresistancemovement.org/?p=9226

Related articles:

See VRM: The Autism Report

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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