Senate Bill SB277, California’s draconian forced vaccination policy for school children in the public school system, will never see the light of day, if teachers and school administrators go on strike to oppose it. We, the people, (not our Government legislators), ‘have the real power.

If it comes to it, California should consider forming a sector of public schools across the State exclusively tailored for vaccine-free children. There are, conservatively, tens of thousands of eligible children ready to fill these seats. 

This could be a turning point for our communities. I guarantee you, the positive ripple effects will quickly resonate throughout the Untied States, and elsewhere. Such is how we start bushfires of freedom in the hearts of our communities around the world.

The conflict looming in California, over the draconian, unlawful Bill, SB277, currently being instated, will have such serious consequences for families, we may be headed toward an open revolt, perhaps something akin to civil war.

Three crucial aspects to consider in respect to local communities affected:

1) Every parent or guardian is bound to protect their child’s inalienable right to self-determination of the body, what goes in it, and if so, administered by whom. The Government has no authority, whatsoever, to regulate, monitor or deny these primary parental rights.

2) It is unconstitutional to deny any child, born in the USA, their inherent right to free & open access to public education. This law therefore infringes on two crucial areas of basic freedom.

3) There will be hundreds of thousands of (unvaccinated) children displaced by this Bill. Their parents will be forced to homeschool their child/children; despite the fact that many of these families are two-income-type households.

California’s new forced vaccination Bill SB277, for children, represents the most draconian, fascist, unlawful health-directive ever to be forced upon the population in the history of the United States.

The whole premise behind personal exemptions was always a ruse.

The freedom to choose what goes into your, body, or into your child’s bloodstream, is non-negotiable. The Government has inverted and overturned this basic principle, and has, thus, bound freedom itself, to a contract. 

Exemptions from Government imposed health mandates were ultimately designed to fail, by entrapping those members of the community who sign onto them, binding them to an arbitrary (constantly changing) list of choices (demands) that supercede said basic freedoms, and thereupon deny an individual their inalienable, God/life given rights to self-determination of the body.

 Regardless of which way the pendulum swings, California is headed towards an imminent, all-out open revolt, nothing short of a groundswell civil war with the Government. Vaccine Resistance Movement



Ebola Liberia

Such an accumulation of overlapping & contradictory scientific evidence begs the question – has the Medical community misdiagnosed Ebola?

Are we actually dealing with a virus here, or a bacterial strain, or in fact, a composite form of virus/bacteria hybrid?

Excerpts from VRM: Ebola Report

Why has the Ebola virus suddenly erupted in a region of Africa known as the “Meningitis Belt” (comprising all four countries affected – Guinea, Liberia, Nigeria & Sierra Leone)?

Because the WHO & CDC are deliberately trying to cover up their bloody tracks.

The recent Ebola outbreak in Africa coincides with a massive Meningitis Vaccine campaign targeting “150 million Africans”, many throughout Guinea & Nigeria.

The cost-effective vaccine, MenAfriVac®, (less than US$0.50 per dose) was “kept outside the cold chain for up to four days at up to 40°C”.

Neighboring Liberia & Sierra Leone, both primary epicenters, were recently subject to the “largest ever Yellow Fever Immunization Program” conducted in that region – an estimated 12 million locals impacted (infected) by the compound shot.

Vaccine Resistance Movement is investigating the link between these extremely toxic experimental vaccines and the sudden surge in cases of Ebola.

Yellow Fever vaccine

Symptoms of ‘Acute fulminating Meningococcal Septicemia’, a virulent form of bacterial meningitis (marked by extreme vomiting, hemorrhaging – excessive bleeding around the eyes & mouth, severe blackish bruising on the arms & legs), leading to Septic shock and potentially even death, closely resemble those seen in Ebola victims.

This supposed outbreak of Ebola bares all the hallmarks of a rarified, virulent strain of bacterial Meningitis, ‘Acute fulminating Meningococcal Septicemia’, also known as ‘Waterhouse-Friderichsen Syndrome’.

Is this yet another case of a dangerous, untested vaccine triggering a tsunami of viral & bacterial mutations – in impoverished regions?

Waterhouse-Friderichsen Syndrome: ‘The prodromal symptoms were similar to those encountered in any respiratory infection, consisting of headache, chilly sensations, muscular pains and malaise. The onset of the bacteremia was sudden and dramatic. The most striking features were the profound shock and the petechial eruption, which in the course of a few hours became purpuric…This condition gradually progressed until numerous coarse, bubbling rales could be heard over both lung fields. With the appearance of frank pulmonary edema terminally, the patient lapsed into coma and died shortly thereafter.

Meningococcal Septicemia (Septic shock): ‘The hallmarks of severe sepsis and septic shock are changes that occur at the microvascular and cellular level with diffuse activation of inflammatory and coagulation cascades, vasodilation and vascular maldistribution, capillary endothelial leakage, and dysfunctional utilization of oxygen and nutrients at the cellular level. The challenge for clinicians is to recognize that this process is under way when it may not be clearly manifested in the vital signs or clinical examination.‘ Andre Kalil, MD, MPH  Professor of Medicine, Department of Medicine, Section of Infectious Diseases; Director, Transplant ID Program, University of Nebraska Medical Center
Note: ‘DIC (Disseminated intravascular coagulation), is most commonly observed in severe sepsis and septic shock. Indeed, the development and severity of DIC correlate with mortality in severe sepsis. Although bacteremia, including both gram-positive and gram-negative organisms, is most commonly associated with DIC, other organisms (eg, viruses, fungi, and parasites) may also cause DIC.

DIC exists in both acute and chronic forms. Acute DIC develops when sudden exposure of blood to procoagulants (eg, tissue factor [TF], or tissue thromboplastin) generates intravascular coagulation. Compensatory hemostatic mechanisms are quickly overwhelmed, and, as a consequence, a severe consumptive coagulopathy leading to hemorrhage develops. Abnormalities of blood coagulation parameters are readily identified, and organ failure frequently results.‘ Marcel M Levi, MD  Dean, Academic Medical Center, University of Amsterdam, The Netherlands

There is no evidence that MenAfriVac can cause meningococcal meningitis. Clinical alertness to the possibility of co-incidental meningitis should be maintained.‘ MenAfriVac® (Package insert)

Ebola virus

Ebola Virus: ‘Generally, the abrupt onset of Ebola haemorrhagic fever follows an incubation period of 2–21 days (mean 4–10) and is characterised by fever, chills, malaise, and myalgia. The subsequent signs and symptoms indicate multisystem involvement and include systemic (prostration), gastrointestinal (anorexia, nausea, vomiting, abdominal pain, diarrhoea), respiratory (chest pain, shortness of breath, cough, nasal discharge), vascular (conjunctival injection, postural hypotension, oedema), and neurological (headache, confusion, coma) manifestations.

Haemorrhagic manifestations arise during the peak of the illness and include petechiae, ecchymoses, uncontrolled oozing from venepuncture sites, mucosal haemorrhages, and post-mortem evidence of visceral haemorrhagic effusions. A macropapular rash associated with varying severity of erythema and desquamate can often be noted by day 5–7 of the illness; this symptom is a valuable differential diagnostic feature and is usually followed by desquamation in survivors. Abdominal pain is sometimes associated with hyperamylasaemia and true pancreatitis. In later stages, shock, convulsions, severe metabolic disturbances, and, in more than half the cases, diffuse coagulopathy supervene.‘ Heinz Feldmann, MD and Thomas W Geisbert, PhD, The Lancet

Ebola Liberia1

The epidemiology of Yellow Fever also bares striking resemblance to Ebola, given the distinct characteristics & potential virulence common to each virus:

1. an incubation period lasting upwards of 1 week (‘Physical symptoms usually appear 3–6 days after’)

2. an array of flu-like symptoms during the initial stages, including (‘fever, muscle pain, particularly backache, headache, shivering, loss of appetite, and nausea or vomiting’)

3. leading to varying degrees of internal “blackish” bruising & widespread hemorrhaging (‘gastrointestinal bleeding, haematuria, skin petechiae, ecchymoses,’)

4. followed by rapid systemic deterioration, marked by Kidney failure, often leading to death (‘About 20%–50% of patients with hepato-renal failure die, usually 7–10 days after the onset of disease’)

Typically, the disease onset is abrupt, with fever, muscle pain, particularly backache, headache, shivering, loss of appetite, and nausea or vomiting. Congestion of the conjunctivae and face are common, as well as relative bradycardia in the presence of fever. The patient is usually viraemic during this period, which lasts for approximately 3–6 days.

In approximately 15% of infected persons, the illness recurs in more severe form after a brief remission of 2–24 hours. Symptoms include fever, nausea, vomiting, epigastric pain, jaundice, renal insufficiency, and cardiovascular instability. A bleeding diathesis can occur causing gastrointestinal bleeding, haematuria, skin petechiae, ecchymoses, epistaxis, and bleeding from the gums and needle-puncture sites.

Physical findings include scleral and dermal jaundice, haemorrhages at different sites and epigastric tenderness without hepatic enlargement. The haemorrhagic manifestations are caused by reduced synthesis of clotting factors as well as by a consumptive coagulopathy.

About 20%–50% of patients with hepato-renal failure die, usually 7–10 days after the onset of disease. Patients surviving YF may experience prolonged weakness and fatigue, but healing of the liver and kidney injuries is usually complete.‘ Vaccines and vaccination against yellow fever/WHO Position Paper – June 2011

Yellow Fever vaccine1

Yellow fever vaccine-associated viscerotropic disease (YEL-AVD) is a rare and serious adverse event associated with administration of the yellow fever vaccine. YEL-AVD is an illness similar to wild-type yellow fever, in which the vaccine virus proliferates in multiple organs, causing multiple organ dysfunction syndrome or multiorgan failure and death in at least 60% of cases. Initial symptoms of YEL-AVD are nonspecific and can include the following: fever, malaise, headache, myalgia, vomiting, and diarrhea. More severe cases can progress to hepatic, renal, or respiratory insufficiency or failure; hypotension; thrombocytopenia; and coagulopathy (inability to regulate clotting causing massive hemorrhaging).‘ CDC – History, Epidemiology, and Vaccination Information

Yellow fever vaccine-associated viscerotropic disease (YEL-AVD) is clinically indistinguishable from wild-type yellow fever illness. Most YEL-AVD reports describe patients with fever and multiple organ system failure, and often death (17 deaths/29 cases worldwide).‘ The American Journal of Tropical Medicine and Hygiene

The present YF vaccines are based on a wild-type YF virus isolated in Ghana in 1927. Numerous mutations in the viral structural and non-structural genes have led to the attenuated variant 17D. This attenuated vaccine virus exists in 2 sub-strains (17D-204 and 17DD) which share 99.9% sequence homology. Nucleotide sequencing has shown differences between these vaccine strains and the wild-type Asibi strain, affecting 20 amino acids. Virus with the resulting phenotype is non-transmissible by mosquitoes. Both sub-strains are used in vaccines prepared by culturing the virus in embryonated eggs. The vaccine contains sorbitol and/or gelatine as a stabilizer and is lyophilized. No preservative is added.‘ WHO Position Paper on Yellow Fever Vaccine


Even the CDC Director admits they are baffled by the unprecedented concentration of cases outside the typical range,

For more than four decades, Ebola virus had only been diagnosed in Central or Eastern Africa. Then late this past March, the first cases of Ebola began appearing in a surprising part of the continent. The outbreak in Guinea was the first sign that the virus had made the jump across the continent. Ebola then spread quickly to Sierra Leone and Liberia, and then to Nigeria.‘ Tom Frieden, MD, MPH, Director, US Centers for Disease Control and Prevention, Atlanta, Georgia

Irrespective of whether we are confronting a vaccine-derived hybrid (mutagenic) strain of bacterial Meningitis here, a vaccine-derived hybrid strain of Yellow Fever, or, in fact,  a laboratory-derived hybrid strain of the Ebola Virus (essentially a composite of the laboratory produced Aids Virus) the so-called vanguard of Health “Authority”, chiefly the CDC & WHO, are purposefully focusing on a Vaccine & Drug response to this current health crisis, while ignoring the fact that the Ebola Virus can only thrive in a body starved of Selenium – thereby depriving our communities of critical information in a time of national emergency.

SeleniumThe Ebola Virus can ONLY thrive in a body starved of Selenium. In fact ALL Ebola Virus victims, those who typically succumb to Hemorrhagic fever, viral replication (infected blood) and excessive hemorrhaging of the blood leading to death, concurrently suffer from acute malnutrition, marked by extreme Selenium deficiency in the body.

Selenium is an essential anti-oxidant, the primary stop-gap which enables the human body to adapt to (overcome) any viral infections circulating in the environment, and prevents the typical Ebola-type symptoms (chiefly excessive hemorrhaging) from taking hold and ultimately killing the host (vaccinee).

Natural sources rich in Selenium include Brazil nuts, Sunflower seeds & Food Grade Diatomaceo​us Earth (“fossilized shell flour”).

Meningitis Vaccine campaign Africa 1

Ebola is classified as a “hemorrhagic fever” virus, and produces the characteristic hemorrhaging due to the formation of blood clots (“disseminated intravascular coagulation”), leading to the obstruction and rupture of small blood capillaries.

It is very well documented that Se (Selenium) plays a significant role in the regulation of blood clotting via its effects on the thromboxane/prostacyclin ratio.

Se (Selenium) has an anti-clotting effect, whereas Se (Selenium) deficiency has a pro-clotting or thrombotic effect. Se (Selenium) deficiency has been associated with thrombosis and even hemorrhaging, which has been documented in a number of animals with severe Se (Selenium) deficiency (often artificially induced), but is almost never seen in humans, probably because such an extreme Se (Selenium) deficiency is rarely attained due to the diversity of human diet.

Our analysis suggests that severe Ebola infections could produce an artificial and extreme Se (Selenium) depletion, resulting in extensive cellular damage due to lipid peroxidation, combined with enhanced thrombosis. This could also contribute to the associated immune deficiency that has been observed in Ebola infections.

If viruses like HIV-1 (Aids), coxsackievirus B3 (linked to Meningitis) and Ebola do encode selenoproteins, why does all the evidence suggest that dietary Se (Selenium) inhibits viral replication, whereas Se (Selenium) deficiency triggers replication?‘ Journal of Orthomolecular Medicine, 1995

Note: ‘…extensive cellular damage due to lipid peroxidation, combined with enhanced thrombosis (excessive blood-clotting – the result of vaccine-derived auto-immune failure in the body).

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

Meningitis Vaccine campaign Africa

History is repeating itself…again.

Once again, just like in 2009, the WHO are purposefully inflating the numbers of victims here, to ensure the maximum fear factor is felt throughout our communities. Until those clinics & hospitals impacted by this crisis release the actual (post mortem) laboratory results, any statistics being foisted on us represent nothing more than speculation at best.

These (Ebola) numbers are subject to change due to on-­going reclassification, retrospective investigation and availability of laboratory results…Work is also ongoing to resolve discrepancies between different sources of data, which may leas to a revision of the numbers of cases and deaths in the future.‘ WHO disclaimer

During the 2009 (CDC bio-laboratory produced) Pandemic. the WHO routinely exaggerated the overall death toll (attributable to H1N1); by including any/all cases associated with Flu-like symptoms – regardless of the fact that the VAST majority of victims inevitably died as a result of compromised immunity and/or pre-existing medical conditions. H1N1 was merely a blip on the radar, by all accounts a comparably mild seasonal flu.

It’s vitally important to analyze the current Ebola scare objectively. Throughout the recent manufactured “Swine Flu” Pandemic of 2009, communities around the world were manipulated constantly by Mainstream Media outlets (in lock-step with the WHO & spineless Government health departments), via an ongoing barrage of misinformation, negative hype & fear-mongering propaganda.

By the time all the dust settled it was unanimously determined by most experts in the scientific arena, “H1N1 has ultimately turned out to be, from a pandemic perspective, a dud.

Fast-forward to 2014 … “As the (Ebola) epidemic gets more and more formidable and in some cases out of control it is quite conceivable, if not likely, that we may need to deploy the vaccine to the entire country to be able to shut the epidemic down. That is clearly a possibility.” U.S. National Institute for Allergy and Infectious Diseases (October 06, 2014)

Don’t allow yourself to be drawn into the propaganda. Within a year, this will, once again, be proven to have originated in a CDC Level 4 laboratory.

* Excerpts from VRM: Ebola Report

Lest we forget?



MMR shot propaganda campaignWhy are clusters of measles outbreaks on the rise? It has nothing to do with the increasing trend toward lower rates of vaccine uptake throughout our communities; the inference that avoiding getting your child “immunized” with the MMR series increases their risk of susceptibility to measles and transference of measles to other children in their proximity.

As Dr Tetyana Obukhanych Ph.D, one of the world’s leading Immunologists (guest speaker at our recent VRM Vaccine Summit) points out, vaccines have stripped mothers, and by extension, their baby, of the capacity for life-long immuno-protection, given the absence of NATURAL childhood exposure to measles in the environment.

Parents who received the first wave of measles shots in 1963 (and all those since) were subsequently stripped of their capacity to transfer natural immuno-protection to their baby, via the Placenta & Colostrum, due to the cross-contamination factor (hybrid measles virus now embedded in the mother/father’s germ line DNA – manifesting in a more virulent strain of measles, known as ‘Atypical Measles’ or AMS) generated by the shot, passed on to the new generation.

The current generation have literally become unwitting hosts to a form of viral & bacterial roulette, an ideal breeding ground for the proliferation/weaponizing of viral & bacterial infections.

Measles virus, TEM

“I am very concerned that “immunologic memory” of adjuvant-containing vaccines is actually the basis of sensitization rather than the basis of immunity. Furthermore, I am very concerned that “successful” prevention of childhood diseases by means of short-term protective effects of live attenuated viral vaccines during childhood has led to the loss of maternal ability to transfer immuno-protection to their young, thereby leaving infants vulnerable to those diseases, should the exposure occur.

I am also very concerned that vaccination campaigns work by disrupting disease transmission, which reduces the chances of exposure, rather than by establishing a population’s immunity. By doing so, vaccination campaigns wipe out population’s immunity to childhood diseases rather than help to maintain it. If in prior decades there was naturally established herd immunity to childhood diseases among the adult population, then I am afraid that vaccination campaigns have ensured that it is long gone.

All of this is a direct outcome of the “desired” vaccination effects, the impact of which hasn’t been carefully thought through in advance of introducing mass vaccination. We thought that vaccines work just like natural immunity. Well, apparently they don’t and we are now reaping the consequences of that.

We would expect that vaccinated individuals would not be involved (or very minimally involved) in any outbreak of an infectious disease for which they have been vaccinated. Yet, when outbreaks are analyzed, it becomes apparent that most often this is not the case. Vaccinated individuals are indeed very frequently involved and constitute a high proportion of disease cases. I think this is happening because vaccination does not engage the genuine mechanism of immunity. Vaccination typically engages the immune response—that is, everything that immunologists would theoretically “want” to see being engaged in the immune system. But apparently this is not enough to confer robust protection that matches natural immunity. Our knowledge of the immune system is far from being complete.” Dr Tetyana Obukhanych Ph.D


We found 18 reports of measles outbreaks in very highly immunized school populations where 71% to 99.8% of students were immunized against measles. Despite these high rates of immunization, 30% to 100% (mean, 77%) of all measles cases in these outbreaks occurred in previously immunized students. In our hypothetical school model, after more than 95% of schoolchildren are immunized against measles, the majority of measles cases occur in appropriately immunized children.

 The apparent paradox is that as measles immunization rates rise to high levels in a population, measles becomes a disease of immunized persons. Because of the failure rate of the vaccine and the unique transmissibility of the measles virus, the currently available measles vaccine, used in a single-dose strategy, is unlikely to completely eliminate measles. The long-term success of a two-dose strategy to eliminate measles remains to be determined.‘ Poland GA, Jacobson RM., Department of Internal Medicine, Mayo Vaccine Research Group, Mayo Clinic and Foundation, Rochester, MN./1994

As one of many examples involving all infectious diseases of childhood against which vaccines have been developed, ever since any measles vaccines have been introduced and used in mass proportions, reports of outbreaks and epidemics of measles in even 100% vaccinated populations started filling pages in medical journals. It is less well known to the general public that vaccinated children started developing an especially vicious form of measles, due to the altered host immune response caused by the deleterious effect of the measles vaccines. It resisted all orthodox treatment and carried a high mortality rate. It has become known as atypical measles (AMS).

In the meantime, outbreaks of measles in vaccinated children have continued and intensified to this day. Contemporary observations of the ineffectiveness of vaccination indicate to me that the incidence of measles has increased and has not continued decreasing as it did for some 100 years before any type of measles vaccination was introduced.‘ Dr Viera Scheibner (PhD), International Medical Counsel on Vaccination

We developed case criteria on the basis of serology and rash distribution and morphology. In typical measles a maculopapular rash occurs first at the hairline, progresses caudally, is concentrated on the face and trunk, and is often accompanied by Koplik’s spots. In AMS the rash Is morphologically a mixture of maculopapular, petechial, vesicular, and urticarial components. It usually begins and is concentrated primarily on the extremities, progresses cephalad, and is not accompanied by Koplik’s spots. Cases were classified as AMS if patients had 1) a rash with the distribution and morphology characteristic of AMS, and 2) a fourfold or greater rise in titer of complement-fixing measles antibody or a convalescent titer of 256.‘ E M Nichols MD


Some vaccines, including the MMR, smallpox, and chickenpox vaccines, contain live viruses. By giving three and sometimes four live viruses together, the risk of developing a lifetime viral infection (a persistent viral infection) increases tremendously. This is especially so with the MMR vaccine, which contains two live viruses known to suppress the immune system for months.‘ Dr. Russell L. Blaylock M.D.

Measles, Mumps, Rubella Vaccine (series) – 1st round given at 12-15 months old: ‘The evidence convincingly supports a causal relationship between MMR vaccine and measles inclusion body enchephalitis (inflammation of the Brain & Meninges/Meningoencephalitis manifesting as ‘diffuse and/or focal neuropsychological dysfunction – reaction to synergistic heavy metal-excipient accumulation of ’sludge’ toxicity) in individuals with demonstrated immune deficiencies.’ P.110 Institute of Medicine Report on Adverse Effects of Vaccines/2011

A mutagenic Measles virus strain commonly infects the bowels/intestines of children with Autism. Merck’s official package insert for the Measles, Mumps, Rubella vaccine explains why: ‘M-M-R II has not been evaluated for carcinogenic or mutagenic potential, or potential to impair fertility.

Measles vaccine can cause problems (e.g. fatal giant cell pneumonia) in those with severely compromised cell-mediated immunity.‘…”I have also found that regressive behavioral disorder (RBD) in children is associated with measles, mumps and rubella (MMR) vaccination. These children all have gastrointestinal symptoms including abdominal pain, diarrhea, and in some cases food intolerance. It is significant that this syndrome only appeared with the introduction of the polyvalent MMR vaccine in 1988 rather than with the monovalent measles vaccine introduced in 1968. This indicates that MMR is responsible for this condition rather than just the measles virus and that accordingly a transfer factor specific for the components other than the measles virus in MMR may be required.”  Dr. Andrew Wakefield   

‘One 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 L. Blaylock

Official Package Insert: 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.’

Note: Dr. Andrew Wakefield’s 1998 Study demonstrated “anti-myelin antibodies and digestive tract pathologies in children with autism after being given the Urabi strain triple live virus MMR vaccine. All 12 children in the Study had intestinal abnormalities (known as Inflammatory Bowel Disease), with chronic inflammation in the colon in 11 of the children. Noted behavioral disorders included autism in 9, disintegrative psychosis in 1, and possible post-viral or vaccinal encephalitis (acute brain inflammation) in 2.

Since that release there have been countless other studies verifying exactly the same pattern – including the presence of measles lingering in the bowels of young children who have gotten of the Measles-Mumps-Rubella shot (MMR).

The Urabi strain MMR vaccine purchased by GlaxoSmitheKline for distribution in the UK, a triple live virus version, was directly responsible for an sudden spike in childhood Meningitis in the UK. It had been banned from use in Canada & was warned against further use in Britain by Canadian specialists. This was all suppressed by GSK & The British Gov’t. They are solely to blame for this crisis.

The Urabe AM9 vaccine was developed in Japan and was originally attenuated by six passages of a wild isolate in chicken amniotic cavity, after which the virus underwent two plaque purifications in quail fibroblasts.

Specifically, the Urabe AM9 component of trivalent measles, mumps and rubella vaccines was associated with meningitis (inflammation of the meninges, the thin, membranous covering of the brain and the spinal cord)and parotitis (inflammation and infection of the salivary glands).

We also demonstrated that these same sequence differences, specifically a subset of mutations in the viral polymerase, control the ability of Gw7 and 1004-10/2 to replicate in human cell lines.’ Identification of Genetic Mutations Associated With Attenuation and Changes in Tropism of Urabe Mumps Virus/Dion Shah, Silvia Vidal, Malen A. Link, Steven A. Rubin, and Kathryn E. Wright

According to the records of the Metropolitan Life Insurance Company, from 1911 to 1935 the 4 leading causes of death from infectious diseases in the USA were diphtheria, scarlet fever, whooping cough (pertussis) and measles. However, by 1945 the combined death rates from these causes had declined by 95%, BEFORE THE IMPLEMENTATION OF MASS IMMUNIZATION PROGRAMS. By far the greatest factors in this decline were sanitation through public health measures, improved nutrition, and better housing with less crowded conditions.

There is a school of thought that the so-called minor childhood illnesses of former times, including measles, mumps, chicken pox, and rubella, which entered the body through the mucous membranes, served a necessary and positive purpose in challenging and strengthening the immune system of these membranes. Vaccines in contrast are injected directly into the body, consequently bypassing the mucous membranes, leaving the mucosal immunity relatively weak and stunted.

In both The New England Journal and the journal Thorax, articles have appeared stating that a healthy immune system has a “bias” towards the cellular immune system, whereas people with allergies, asthma, and diseases of an autoimmune origin have a humoral-dominant (vaccine derived antibody-mediated) system. It has also been shown that, once one of these subsets become dominant, it is difficult to shift the system to the other subset.‘ Dr. Harold E. Buttram, MD

Government data admits to a probable causal link between vaccines & the presence of Measles in the bowels of young children (related to Inflammatory Bowel Disease); while promoting a deliberate cover-up of these inherent risks to the general public,

‘That Crohn’s disease and other chronic inflammatory illnesses of the intestine might be caused by a virus such as measles is an interesting hypothesis. Until the present time, microbiologic and epidemiologic arguments either for or against this hypothesis have not been very convincing. It is not very likely that other epidemiologic studies will provide conclusive evidence. In fact, it would be difficult to find a population that includes both individuals who have been exposed to the virus or to the vaccine and individuals who have not been exposed. However, new microbiologic studies might prove conclusive.

First, it would be necessary to demonstrate that the measles virus is indeed present in the lesions, that it is active, and that it contributes to inflammatory responses. Also, it would be necessary to prove that the pathogenic reaction can be induced by the wild virus and by the attenuated viruses present in vaccines. Strains and attenuation procedures vary from one manufacturer to another, and it is far from certain that all strains have the same ability to persist in tissues and to subsequently produce chronic inflammations. As was stated above, measles vaccine does not seem to be associated with SSPE, although the wild virus may be isolated (with difficulty) in patients with SSPE. The measles virus was isolated neither in patients with Crohn’s disease or other chronic inflammatory diseases (Paget’s disease, active chronic hepatitis, multiple sclerosis) in which a role for it has been claimed on morphologic, histologic or serologic grounds.

Current scientific data do not permit a causal link to be drawn between the measles virus and chronic inflammatory bowel diseases. While awaiting production and publication of other research, it would not be appropriate to alarm recipients of the vaccine by notifying them of this hypothetical risk, thus jeopardizing an immunization program of proven benefit.’ Public Health Agency of Canada

Scandalous cover-up:  “…it would not be appropriate to alarm recipients of the vaccine by notifying them of this hypothetical risk, thus jeopardizing an immunization program of proven (cost) benefit.

Despite the advantages of live, attenuated vaccines, there are some downsides. It is the nature of living things to change, or mutate, and the organisms used in live, attenuated vaccines are no different. The remote possibility exists that an attenuated microbe in the vaccine could revert to a virulent form and cause disease.‘ US National Institute of Allergy and Infectious Diseases

 Note: ‘The remote possibility exists that an attenuated microbe in the vaccine could revert to a virulent form and cause disease.

One vaccine decreases cell-mediated immunity by 50%, two vaccines by 70%…all triple vaccines (MMR, DTaP) markedly impair cell-mediated immunity, which predisposes to recurrent viral infections, especially otitis media, as well as yeast and fungi infections.”  World-renowned Immunologist Dr. H.H. Fudenberg

If vaccinated children and adults are capable of spreading disease, shall we hold them and their parents legally liable for outbreaks? Shall we mandate ‘unvaccination’ as a requirement for public school? Since we can’t ‘unvaccinate,’ shall vaccinated children be kicked out of public school?‘ Toni Bark, M.D.

Excerpts from  VRM: MEASLES REPORT

See VRM: The Rise of Mutagenic Viruses

See VRM: The Autism Report

Vaccine Resistance Movement


Cancer research fraud1

Every Vaccine in circulation is required to undergo Clinical Trials before being granted sale onto the market. The Vaccine Industry uses a statistical measure called “relative risk” (rather than “absolute risk”) to deliberately bury/obfuscate any direct causal link between the vaccine itself and subsequent neurological & neurodevelopmental damage incurred.

This enables them to minimize or eliminate altogether, the extent of negative trial data potentially hindering the glowing track-record of the product. Therefore, any/all cases of Sudden Infant Death, Encephalitis, Anaphylaxis, Seizures, etc. etc. etc….detected in the hours/days post inoculation, are never recorded in the final analysis (equation), cancelled out by the total number of percentages. It’s nothing but a shell game.

An important feature of relative risk is that it tells you nothing about the actual risk. This can be very important for evaluating how significant a relative increase might be.‘ George Mason University

…even when an investigator has had substantial input into trial design and data interpretation, the results of the finished trial may be buried rather than published if they are unfavourable to the sponsor’s product.


THE DARK HISTORY OF THE HEPATITIS B VACCINE – 3 doses given, 1st round administered at 12 hours old (after birth):

hep-b-vaccineResearch scientists have now identified a direct causal link between subcutaneous &/or intramuscular injection of the Hepatitis B Vaccine and resulting Mitochondrial dysfunction (hallmark symptom of Autism); including premature apoptosis or “programmed” type cell death. Hep B vaccine factors into eventuality of Early Onset Autism, since it represents the earliest premature breach of a baby’s delicate, under-developed “electrical grid system” (Myelin sheath, Meninges & Blood Brain Barrier).

WILLOWBROOK STATE SCHOOL FOR MENTALLY CHALLENGED (Staten Island, NY )/196O’s – Mentally challenged students (inmates) were forcibly injected with cancerous Hepatitis B shots. Thousands infected, hundreds died.

WillowbrookDr. Saul Krugman of New York University conducted studies of hepatitis during the 1950s and 1960s on the severely mentally retarded. He systematically infected newly arrived children between the ages of three and eleven with strains of the virus obtained from the feces of Willowbrook hepatitis patients.

This was done to study the natural history, effects, and progression of the disease. Franz Inglefinger, who later became the editor of the New England Journal of Medicine said, “By being allowed to participate in a carefully supervised study and by receiving the most expert attention available for a disease of basically unknown nature, the patients themselves benefited.

How much better to have a patient with hepatitis accidentally or deliberately acquired under the guidance of a Krugman, than under the care of a rights-minded zealot.”‘ Excerpt from Carol Rutz’s Lecture at Indiana University, November 2003

Dr. Krugman, the author of well over 200 scientific papers, received many honors in this country and abroad, including a medical research award for public service in 1983 from the Albert and Mary Lasker Foundation. Its citation said that Dr. Krugman had provided “critically important studies of hepatitis, rubella and measles.” It singled out his pivotal role in creating a vaccine against the hepatitis B virus.‘ New York Times

Exposure of Hepa1-6 cells to a low dose of adjuvanted hepatitis B vaccine leads to loss of mitochondrial integrity, apoptosis induction, and cell death…‘In vivo apoptotic effect of hepatitis B vaccine was observed in mouse liver.‘…’Boys vaccinated as neonates had threefold greater odds for autism diagnosis compared to boys never vaccinated or vaccinated after the first month of life. Non-Hispanic white boys were 64% less likely to have autism diagnosis relative to nonwhite boys. Findings suggest that U.S. male neonates vaccinated with the hepatitis B vaccine prior to 1999 (from vaccination record) had a threefold higher risk for parental report of autism diagnosis compared to boys not vaccinated as neonates during that same time period.

Official Package Insert: ‘10 µg/mL  Each 1 mL dose of sterile suspension contains hepatitis B surface antigen 10 µg adsorbed onto approximately 0.5 mg of amorphous aluminum hydroxyphosphate. Formaldehyde-treated. Thimerosal (mercury derivative) 1:20,000 (50 µg/mL) has been added only to the preservative-containing formulations. 3-dose vials of 3 mL‘…’A portion of the hepatitis B virus gene, coding for HBsAg, is cloned (synthetic genomics) into yeast, and the vaccine for hepatitis B is produced from cultures of this recombinant yeast strain.

Think about it. Vaccine Resistance Movement  


H1N1 hype

The Flu Vaccine deception ranks as one of the great cover-ups & swindles of the last century perpetrated against the general population. Not only has the public been systematically lied to by their elected Gov’t for generations (in league with the World Health Organization & a Vaccine Industry Medical Mafia feeding trough), but the entire bedrock of our natural immunity has been put at risk through the collision of forces being pitted against us around the world.

The business of the Vaccine Industry represents a multi-billion dollar enterprise, and countries around the world (194 signatory nations under the banner of a World Health Organization treaty) are literally “bound” to this bottomless swindle – our communities the intended “target market” fodder. ‘The International Health Regulations (IHR) is an international legal agreement that is binding on 194 States Parties across the globe, including all of the Member States of WHO.

Once again this year, Government “Health Officials” & Mainstream Media outlets are in unison, using the same desperate tactics they employed during 2009, the marketing ploy of “artificial scarcity”, withholding vaccine supplies long enough to create the PERCEPTION of a shortage, while reinforcing the myth of herd immunity compliance locally; banner headlines of crowds “flocking” to emptied-out clinics, panic everywhere, all in a desperate attempt to frighten the public into getting the Flu shot.

Just remember,  65-70% of our community are REFUSING to get the Flu shot every year. Statistically, 70% of Canadians are REFUSING to get the Flu shot every year…only 30% of Canadians in compliance (based on Statistics Canada: Annual rates): 25-28% of males get the flu shot, while 30-33% of females get the flu shot.

The current US influenza vaccination rate (for all adults 18 years and older) ranges from ’28.0% to 36.2%.

Herd Immunity
The Flu itself cannot kill you; rather the result of acute bacterial pneumonia triggered BY Flu-like symptoms. Most victims of the Flu are those 65 years and older. In almost every instance a compromised immune system and/or a pre-existing medical condition is the key determinant factor in those unfortunate victims (at whichever age) who die from the Flu.
H1N1 hype 2014

1. Flu deaths are attributed primarily to bacterial pneumonia triggered by the flu symptoms. The flu itself cannot kill you

2. Most victims of the flu are those 65 years and older

3. In almost every instance a compromised immune system is a key factor in those victims who succumb to the flu

4. Most children who succumb to seasonal Flu, either via death or serious long-term illness (in particular those tracked since 2009), are subsequently found to have been 8 times more predisposed to a Methicillin-resistant Staphylococcus Aureus (MRSA) bacterial co-infection occurring in the lungs.

It is also significant that routine prescription anti-bacterials/virals (chiefly Vancomycin Hydrochloride Capsules & Oseltamivir/Tamiflu), widely distributed globally to ostensibly combat flu-like symptoms, have in fact been the tipping point which has worsened such conditions, hastening Kidney failure, Myocarditis (inflammation of the Heart Muscle) & numerous instances of sudden death.

Think about it. Vaccine Resistance Movement

See VRM: Primary Reasons Not To Get The Flu Shot


Foreign DNA

A growing number of children with Autism are now potentially cross-infected with SV40 (diseased African Green Monkey kidney derived Polio virus) type hybrid strains of Poliomavirus (67% infection with Simian Virus); based on a recent Controlled Study which found poliomavirus infection in postmortem brains of sufferers of Autism – inevitably the result of inter-generational cross-contamination from Salk & Sabin Polio inoculations, sugar cube/oral drops versions & the subsequent Inactivated Polio Vaccine now on the schedule; fixed in the germline DNA of babies/children.

BKV (BK Virus- human polyomavirus that causes widespread infection in childhood and remains latent in the host), JCV (JC Virus -type of human polyomavirus or papovavirus), and SV40 (Simian Virus 40) combined are significantly more frequent among autistic patients compared to controls (67% versus 23%, respectively; P <.05).

In recent years more than 60 scientific studies have found SV40 in rare human brain, bone and lung-related cancers, the same kinds of tumors the virus caused in laboratory animals. Some scientists believe SV40 may play a role in causing those cancers. One of the biggest mysteries however, is why SV40 has been found in tumors removed from people who never received the contaminated Salk vaccine.

Mutations and minority variants, relative to vaccine strains, not known to affect attenuation were detected in OPV, mumps virus, and varicella-zoster virus. The anticipated detection of endogenous retroviral sequences from the producer avian and primate cells was confirmed. Avian leukosis virus (ALV), previously shown to be noninfectious for humans, was present as RNA in viral particles, while simian retrovirus (SRV) was present as genetically defective DNA.’ Journal of Virology, June 2010 vol. 84 no. 12

Note: ‘simian retrovirus (SRV) was present as genetically defective DNA.’

Inactivated Polio Vaccine – Official Package Insert: ‘Each dose (0.5 mL) of trivalent vaccine is formulated to contain 40 D antigen units of Type 1, 8 D antigen units of Type 2, and 32 D antigen units of Type 3 poliovirus. For each lot of IPOL vaccine, D-antigen content is determined in vitro using the D-antigen ELISA assay and immunogenicity is determined by in vivo testing in animals. IPOL vaccine is produced from vaccine concentrates diluted with M-199 medium. Also present are 0.5% of 2-phenoxyethanol and a maximum of 0.02% of formaldehyde per dose as preservatives. Neomycin, streptomycin and polymyxin B are used in vaccine production, and although purification procedures eliminate measurable amounts, less than 5 ng neomycin, 200 ng streptomycin and 25 ng polymyxin B per dose may still be present. The residual calf serum protein is less than 1 ppm in the final vaccine.

See: VRM: The Autism Report

Silent No More Project - DVD cover page

Please consider supporting the ongoing efforts of VRM in awakening our communities to Vaccine Industry malfeasance & the paradigm shift toward self-sufficiency & holistic health.

The Vaccine Resistance Movement is finally in a position to reach families throughout the community with this powerful message of self-sufficiency & key steps to take in the paradigm shift toward self-determination of the body…

This important gathering marked the first big push forward following our recent VRM Vaccine Summit. The VRM Silent No More Project brings together some of the same parents of vaccine-injured children in a more intimate setting. Vaccine Researcher Joel Lord also conducts an extensive presentation on the Autism epidemic, synergistic toxicity, demyelination & blood-brain barrier threshold in babies, with a detailed Powerpoint presentation. 2 disks and over 4 hours of ground-breaking footage.

Anyone in the community able to donate $25 or more to VRM will be honoured with a personal, signed copy of the upcoming ‘VRM: Silent No More Project’ DVD – while supplies last. Ongoing availability of this release to a wider community is contingent on us reaching a minimal goal of financing. So I am reaching out to you now.

For those able to donate $50 or more, I will send you a signed copy of the bound booklet version The VRM Autism Report or The Problem With Vaccines Part 4 – Primary Aspects of Vaccine Toxicity Affecting The Body, both of which have been expanded for this special edition (while supplies last); in addition to a signed copy of the VRM Silent No More Project DVD.

For donations of $100 or more  I will send you a signed copy of the bound booklet version The VRM Autism Report  plus The Problem With Vaccines Part 4 – Primary Aspects of Vaccine Toxicity Affecting The Body, both of which have been expanded for this special edition (while supplies last); in addition to a set of signed copies of the VRM Silent No More Project DVD.

Please see the orange tab Paypal link on the VRM website (click on ‘Donate Online’). Thank you all. Joel Lord, founder of The Vaccine Resistance Movement



A great inspiration of mine has just passed away. Dr. Andrew Moulden, an extraordinary font of knowledge who challenged the entire basis of vaccination using the science of the body, a true pioneer in the field of vaccine research, who broke through all the Industry lies & rhetoric by identifying the root cause in ALL cases of vaccination-induced neurological & neurodevelopmental trauma…Ischemia.

If it weren’t for Dr. Andrew Moulden’s extraordinary research, I would never have found my way to the heart of the matter as a vaccine researcher.

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

Through my extensive research and my work throughout the years, I have discovered that vaccinations are causing impaired blood flow (ischemia) to brain and body from clinically silent to death. These are strokes – across the board for all of us. I have reason to believe that all are being affected and all vaccinations ARE causing the overwhelming rise in autism, specific learning disabilities, attention deficit disorders, sudden infant death, gulf war syndrome, dementia, seizure disorders, some cancers it would appear, and much much more.

The brain and nervous system is wired in a very specific format. Functions are localized to specific areas. Having studied brain and behavior, neurosciences, clinical neuropsychology, child neurodevelopment, functional brain imaging, clinical neurology, clinical neuropsychiatry, clinical medicine, immunology, hematology, tests and measurement, and understanding the tools and assumptions and techniques of mainstream medicine, I fell in the unique position of having being able to see clinical medicine problems, from a multitude of simultaneous areas of expertise and scientific knowledge. Relative to the human brain, I understood “rules and laws” of brain function relative to brain damage and the mechanisms of medical physiology that can uniquely cause unique patterns of brain damage in ways that my clinical skills could detect, that mainstream neuroimaging cannot. The initial “aha” moment was in 2001.

I was seeing, autistic patients, coming out of medical school – they had a trans-cortical motor aphasia, isolation of speech syndrome, and very specific cranial nerve palsies that could ONLY be accounted for by ischemic stroke. Remarkably, my studies of schizophrenia, dementia, and research exposure to neuroimaging modalities and brain and behavioral assessments before medical school contributed to my ability to “see” what has been in front of our eyes all along – ischemic strokes and brain damages – from vaccinations. The problem has been we neither knew how to measure, when to measure or what to measure, let alone what the limitations were, of the tools we have been using to measure brain integrity, in health, disease and disorder. It has taken the past several years to decipher how ischemic brain damages were happening in the autism we were seeing and the many other neurodevelopmental disorders. I now believe I have the answers for this, or so it appears and some solutions.

Wild polio caused the exact same brain damages as ALL other vaccines are. Indeed, Guillian Barre syndrome and a host of other neurological disorders is being caused by a common mechanism of injury – albeit from different triggers for different individuals. This is ischemia – from impaired blood flow in microcirculation units. We simply did not appreciate what was right before our eyes. My first cases included several Autistic and Schizophrenic patients. They were showing the exact same acute onset palsies – paralysis. These brain damages were subtle – but measurable multiple, and were present in the pre-vaccine era for wild viruses like polio and infantile paralysis. Once I was armed with the knowledge and skills of a medical doctor, a clinical neuropsychologist, a child neurodevelopmentalist, with research experience in neuroimaging, tests and measurement, scientific method design and analysis, functional localization of brain and behavioral disorders, and a broad base across several other scientific disciplines, I was able to see “the whole forest” despite the trees. Quite literally, I believe I have found and discovered a common mechanism towards acquired human disease and disorder – all of it. It is truly humbling.‘ Dr. Andrew Moulden

The viscosity of this toxic sludge resulting from vaccines which accumulates in the organs (ie. heart, liver, kidney, spleen), 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 can 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/singes the vast network of arterial veins & capillaries leading to the brain, inducing Ischemia.

Here’s one of those rare moments captured when a brilliant mind, unfettered by mainstream academic dogma,  soars on the wings of truth.

‘During times of universal deceit, telling the truth becomes a revolutionary act.’ George Orwell 

Andrew, may you rest in peace.

Vaccine Resistance Movement  



The only purpose for modern hospitals should be that of promoting the betterment of life (including that of life-saving triage surgery).

Instead, most current hospitals are designed primarily to further the massive profits of Institutionalized long-term “chronic” care & Western Allopathic ‘”symptom-based” Medicine.

When was the last time a major hospital explained to a family the benefits of using apple cider vinegar & baking soda, or handed out samples of curcumin, apple, apricot & pumpkin seeds, or Burdock Root, or nascent iodine…or invested in Hyperbaric Oxygen chambers instead of more CT Scanning machines & chemotherapy wards…

Use of CT Scans for Cancer Diagnosis/Treatment: ‘Computed tomography (CT) is a diagnostic procedure that uses special x-ray equipment to obtain cross-sectional pictures of the body. In cancer, CT is used to detect a tumor, provide information about the extent of the disease, help plan treatment, and determine whether the cancer is responding to treatment. A CT scan uses slightly more radiation than a chest x-ray, but the benefits generally outweigh the risks.’ National Cancer Institute

‘Hospitals Performed Needless Double CT Scans, Records Show: In 2008, about 75,000 patients received double scans, one using iodine contrast to check blood flow, and one that did not. “If you do both, you bill for both,” Dr. Pentecost said. A single CT scan of the chest is equal to about 350 standard chest X-rays, so two scans are twice that amount.’ New York Times

Note discrepancy: ‘A CT scan uses slightly more radiation than a chest x-ray (NCI) VS. ‘A single CT scan of the chest is equal to about 350 standard chest X-rays (NYT)

Hyperbaric Oxygen Therapy (HBOT) rapidly eradicates cancer cell growth & quickly restores cell vitality to effected areas in the body without the toxic side-effects associated with Conventional Western Allopathic methods (ie. Chemotherapy); however it is not being applied readily or effectively where it is needed most. ‘Some, but not very many, hospitals have a hyperbaric chamber. Smaller units may be available in outpatient center.‘ This despite the fact that it can be made cost effective for patients, with promising results currently demonstrated in Britain.

HBO treatment for radiation injuries works by increasing the oxygen supply to damaged tissue. This encourages new blood vessels to grow and the tissues to heal. Research has shown that HBO therapy may help reduce cancer growth result in an increase in the body’s own stem cells, which are blood cells at the earliest stage of development in the bone marrow – because HBO therapy can increase stem cells it may have a role in stem cell transplantation, which is a treatment sometimes used in haematological cancers.

Hyperbaric oxygen — 100 percent oxygen at two to three times the atmospheric pressure at sea level — can result in arterial oxygen tension in excess of 2000 mm Hg1 and oxygen tension in tissue of almost 400 mm Hg.2,3 Such doses of oxygen have a number of beneficial biochemical, cellular, and physiologic effects.’ New England Journal of Medicine

‘We just finished HBOT with our son…had improvements in fine and gross motor skills as well as RECEPTIVE language. We did an hour a day from May 2011 until this month.’ VRM member, parent of child coping with Autism



Vaccine surplus

On average, 70% of Canadians are REFUSING to get the Flu shot every year…only 30% of Canadians in compliance (based on Statistics Canada: Annual rates) 25-28% of males get the flu shot, while 30-33% of females get the flu shot. Bravo!
Typically, 50-70% of nurses & doctors (front-line workers) refuse the flu shot. In Canada, this trend was noted long before 2009. ‘Only 43 per cent of acute care staff and 68 per cent of residential care staff on average had the flu shot from 2005 to 2009, according to Vancouver Coastal Health.‘ The remainder, approximately 20.4 million doses ($150,000,000+) were incinerated, a total of $200,000,000+ worth of unused H1N1 vaccine (50% of total investment).
Canada ordered 50.4 million doses of H1N1 vaccine during the Pandemic in 2009, costing the taxpayers $400,000,000+. According to Health Canada, 45% of Canadians received the shot (on average). 5 million doses were donated to the WHO (to be sent to Africa, Asia & Eastern Europe). Another 5 million doses were “loaned out” to Mexico. The Canadian federal gov’t has since announced a new 10-year pandemic flu vaccine contract with GlaxoSmithKline, valued at more than $425-million (in addition to a 3 yr $33-million contract to Sanofi Pasteur Ltd & a $50-million contact to Novartis, a total investment of $500 million+). The contract is intended to ensure a secure supply of vaccine for Canadians in the event of “a future influenza pandemic”.

Canada needs a national vaccination registry so no child misses out on being immunized. A registry would help the government track how many people across the country have been vaccinated. There’s also a need for a co-ordinated national campaign to counter anti-vaccine voices.‘ Canadian Public Health Association

In the US, on average, only 35% of children are receiving the flu shot every year, 25-30% of adults, 63% of seniors over 65 – an indication of growing distrust in immunization policy as a means of strengthening immunity.  ‘If the trend continues this season, overall coverage will still remain substantially below the Healthy People 2020 influenza vaccination targets.‘ CDC   

Vaccine Resistance Movement

See VRM: 5 Reasons Not To Get The Flu Shot

See VRM: Pandemic Preparedness & The Dark Agenda Ahead


pineal_glandMelatonin & The Pineal Gland: 

The Pineal Gland, considered the master gland, which oversees the entire process of metabolic function in the body, ‘five times superior to glutathione in scavenging free hydroxyl radicals‘ (referred to as the ‘third eye’ in ancient cultures), traditionally grew to the size of a quarter in the human body, before the introduction of sodium fluoride into the water supply & widespread use in toothpaste products – when natural immunity could thrive unhindered by such toxic detritus.

Today, the average size of the Pineal Gland in most consumers in the west has diminished to that of a withered dime.

In mammals, the pineal gland is located above the thalamus of the brain between the cerebral cortices. In the 1990s, Jennifer Luke of the UK discovered that the pineal gland is a major site of fluoride accumulation within the body – with higher concentrations of fluoride than either teeth or bone. Luke’s studies indicate that the accumulation of fluoride in the pineal gland can reduce the gland’s synthesis of melatonin, a hormone that helps regulate the onset of puberty. Fluoride-treated animals were found to have reduced levels of circulating melatonin and an earlier onset puberty than untreated animals. Luke concluded:

“The safety of the use of fluorides ultimately rests on the assumption that the developing enamel organ is most sensitive to the toxic effects of fluoride. The results from this study suggest that the pinealocytes may be as susceptible to fluoride as the developing enamel organ”

The pineal gland is innervated by sympathetic axons and by axons coming directly from the brain. Besides sympathetic innervation, the pineal gland receives axons directly from the brain that enter through the stalk. The function of these fibers relative to the physiology of the pineal is unknown.‘ Vollrath L. Functional anatomy of the human pineal gland

pineal gland1Ancient manuscripts call the different glands in the body seals, and by a seal, we mean something which opens and closes. Ancient medical literature states that the glands actually operate according to frequency, a term which is becoming very popular these days in nuclear and quantum physics. The frequency of the glands was known thousands of years ago, but we have forgotten much of this information. In ancient terms, the pineal gland was called the sixth seal or sixth gland of the body.

We have recently discovered that it stimulates two major hormones called serotonin and melatonin.

The pineal gland controls the five other glands below it which are the thyroid which produces thyroxine to energize our cells, the thymus which protects you against infections and cancer, the pancreas which is involved with blood sugar and secreting the hormone insulin, the adrenal gland which responds every time you are under stress; and the first gland is the male and female sex organs and their hormones. Therefore restoring the sixth gland, the pineal gland, will have an impact on all those other glands and their functions in the body. When the pineal gland is at its peak performance, it turns a golden colour and emits a black juice as well as a golden oil. That black juice would be the melanin colour of the organs and every other area of the body which has a pigment.‘ Dr. Mona Harrison

thyroid1The Thyroid Gland is critical in the body. The extent of its ability to function normally determines your degree of overall heath. It is a bell weather indicator. A compromised immune system is much  more vulnerable to infection & seasonal influenza. Vaccines target/undermine the Immune system by introducing live viruses & toxic heavy metals to an already overloaded network; systematically stripping the body of its capacity to harness vital trace minerals (chiefly Selenium, Zinc, Magnesium) & antioxidants (chiefly Vitamins A, B6/B12, C, D3, E + Glutathione).

The synergy of immunological, neurological &  physiological well being hangs in the balance. Thus the delicacy of our glands must be protected. Otherwise a domino effect of sickness & long term deterioration of health are inevitable.

It is known that melatonin scavenges oxygen and nitrogen-based reactants generated in mitochondria. This limits the loss of the intramitochondrial glutathione and lowers mitochondrial protein damage.‘ León J, Acuña-Castroviejo D, Escames G, Tan DX, Reiter RJ., Department of Cellular and Structural Biology, University of Texas Health Science Center, San Antonio, TX

Because melatonin can cross the blood–brain barrier easily, there is much interest in the therapeutic use of this agent in oxidative brain injury. It has been shown previously in our laboratory that melatonin is able to bind to iron. In the present study the level of lipid peroxidation in the melatonin and Fe2+-treated rats was reduced by ± 50%. Thus, the injection of melatonin significantly inhibited lipid damage in the hippocampus induced by the neurotoxin.‘ Journal of Neurochemistry

A study conducted by Pal and Chatterjee suggested that melatonin supplementation in arsenic-treated rats reduces free radical-mediated cytotoxicity and thereby helps in the restoration of normal cellular antioxidant status. The antioxidant effect of melatonin has been claimed as a protective factor towards carcinogenesis, neurodegeneration and aging. A study by Kim et al suggested that immunotoxicity induced by lead was significantly restored or prevented by melatonin (MLT). Splenic T and B cells were significantly increased by MLT treatment when compared with the treatment of Pb alone. The natural killer cell, phagocytic activity and the number of peripheral leukocytes were significantly enhanced in Pb plus MLT-treated mice when compared with the treatment of Pb alone.

The antioxidative effect of melatonin has also been reported by its ability to protect haematopoietic cells from the damaging effects of exposure to lead. The protective effect of melatonin against lead-induced toxicity is attributed mainly to its lipophilic and hydrophilic nature as well as to localize mainly in a superficial position in the lipid bilayer near the polar heads of membrane phospholipids. Since membrane functions and structure are influenced by proteins in membranes, and lead is known to damage thiol proteins, it is possible that the protective action of melatonin to membrane damage induced by lead may be related partially to the ability of the indole group present in melatonin to prevent protein damage. It has also been reported that melatonin stimulates superoxide dismutase mRNA levels in several tissues.‘ Flora, S.J.S.; Mittal, Megha; Mehta, Ashish, Indian Journal of Medical Research

Note: Any product that replicates a naturally occurring substance in the body, such as Melatonin supplement, should be used sparingly, as it can undermine the effectiveness of the Thyroid Grand, by unleashing an over-abundance of free-radicals, triggering hyper/hypothyroidism. Just be prudent, and monitor your health effects on a day-to-day basis, or that of your child, while on these products.  Holistic health requires constant attention to the delicate balance of myriad inter-dependent systems at work; otherwise you’ll often cause a chain reaction elsewhere, by overloading or over-stimulating one component of the body.

Vaccine Resistance Movement



The cream of the crop in the Medical community are immediately sought after in Medical School by Vaccine Manufacturing giants long before they graduate, with the eventual promise of scientific research grants, lucrative payoffs & promotions for product endorsements at medical seminars, through the commissioning of fraudulent clinical trials, including the luxury of all expenses paid weekend getaways, and other incentives once they graduate to top positions in major hospitals & clinics (such as unlimited access to free samples & donated medical equipment).

In return, these obliging doctors must tow the line and push these Vaccines on our communities, without reservation. For some, whose values were compromised early enough, the original meaning of the Hippocratic Oath, “Thou Shalt Do No Harm” has long since lost to the lustre, the lure and the prestige afforded by the almighty dollar.

Regrettably, most Pediatricians are completely in dark on these crucial aspects of vaccine-derived synergistic heavy metal/excipient derived toxicity associated with early childhood immunization, the acute vulnerability of a baby’s brain & central nervous system properties (Myelin Sheath, Blood-brain barrier, Meninges). Almost all mainstream Pediatricians are loathe to promote the benefits of holistic health, as it contravenes the bottom line business practice of peddling prescription drugs & vaccines on the community at large. Self-reliance & optimal natural immunity is not in their best interest.

Their education is specifically limited & tailored to the scope of that which supports the advancing of the Industry food-chain of profits, under the banner of “herd immunity”. The human cost is typically overlooked and under-reported. This wide gulf in understanding can be explained.

According to Dr. Russell Blaylock, world renowned former brain surgeon, the average doctor receives the equivalent of a weekend seminar, in their first year only, on the specific topic of the neurological side-effects & disorders associated with vaccine uptake; approximately seven hours of careful, focused study into the complex strata of auto-immune breakdown type complexities. Without this fundamental bedrock of knowledge a critical component is missing from any doctor’s arsenal, considering the widespread impact neurological side-effects to vaccines have had on the community at large.

‘No medical man during his student days is taught to think. He is expected to assimilate the thoughts of others and to bow to authority. Throughout the whole of his medical career he must accept the current medical fashions of the day or suffer the loss of prestige and place. No public appointments, no coveted preferments are open to the medical man who declines to parrot the popular shibboleths of his profession. His qualifications may be beyond reproach, he may in himself possess qualities that command respect, but unless prepared to think and act within the narrow circle of accepted dogmas, he must be prepared for a more or less isolated path.’ Dr. Walter Hadwen, M.D., UK

Vaccine Resistance Movement


VRM Breaking News – Buried history finally uncovered. The founder of Merck & Co., manufacturer of the HPV Vaccine ‘Gardasil’, was also former chairman of the Biological Warfare Committee of the US Army Chemical War Service during WW2

George W. Merck-1894-1957

George W. Merck, grandson of Heinrich Emanuel Merck (founder of the German-based drug-manufacturing firm ‘E. Merck AG’), took over the US branch of the pharmaceutical firm, known as ‘Merck & Co.’, in 1925. According to officially “withdrawn” documents (see Keesing’s Contemporary Archives, London, February 2-9, 1946), George W. Merck was appointed ‘Official chairman of the Biological Warfare Committee of the US Army Chemical Warfare Service’, during WW2. In 1942 he was authorized, by President Roosevelt, to study & manufacture biological weaponry for the US Military.

Fort Detrick, Maryland‘The idea of biological weaponry was controversial, since little was known about the predictability or effectiveness of biological weapons in wartime. President Roosevelt approved the plan in 1942, and the War Reserve Service, headed by George W. Merck, was established and attached to the Federal Security Agency, a New Deal agency of the Department of Agriculture. The War Reserve Service started out in mid 1942 with a budget of $200,000. Secret work began under Merck’s direction at 28 American universities, including Harvard, Stanford, and other top schools. This agency received consultative advice from national scientific committees and organizations, including the National Academy of Sciences and the National Research Council.

Chemical Warfare ServiceThe War Reserve Service also empowered the U.S. Army’s Chemical Warfare Service to greatly expand its efforts in regard to biological weapons. The army’s efforts were better funded than those of the War Reserve Service: in 1942 and 1943, the Chemical Warfare Service received millions of dollars to build research facilities. Several locations were selected for the army’s biological research, with the main headquarters at Camp Detrick, Frederick, Maryland, a small National Guard airfield (designated Fort Detrick in 1956).

The army also made plans to build a manufacturing plant near Terre Haute, Indiana, and built a 2,000-acre field test site on Horn Island in Pascagoula, Mississippi. It is ironic that much of the United States’s biological warfare effort during World War II was in response to a perceived threat from Germany, when in fact the Japanese were much more actively building their biological warfare capability.’ THE U.S. BIOLOGICAL WARFARE AND BIOLOGICAL DEFENSE PROGRAMS/DAVID R. FRANZ, D.V.M., PH.D.; CHERYL D. PARROTT; & ERNEST T. TAKAFUJI, M.D., M.P.H.

See VRM: Gardasil/Cervarix – A Legacy Of Shame

See VRM: Gardasil/Cervarix Part 2 – Demyelination, Multiple Sclerosis & the Copaxone Connection


Police State

The modern healthcare system, like any powerful corporation, is designed to favor those who acquiesce with their rules & regulations; likewise to weed out & alienate those who do not fall into line with the rest of the “herd”. The entire cesspool of Western Allopathic Medicine, fueled by a medical mafia monopoly, dominates our lives through an endless barrage of mainstream media propaganda, a giant social engineering model, run by select commitees of overpaid Technocratic Elites – void of any decent moral code of ethics, adherence to the Hippocratic oath or underlying sense of altruism toward humanity. How do we avoid their calibrated landmines, and retain what little we can of self reliance and self-sustaining capacity for natural immunity in these tyrannical times? We must reluctantly go along with their manufactured guidelines, in order to stand clear from the rest of the herd.

It is important to understand that ANY/ALL exemptions pertaining to standard immunization vaccines (medical, religious or moral/personal belief type) are fundamentally illegal, because they tranpose an inherent human RIGHT into a PRIVILEGE, on the presumption that you acknowledge and thus sacrifice your natural born “freedom of choice” to an external authority. This is the basis of the looming collectivist (authoritarian) model being rolled out worldwide – the complete isolation of non-conformists and critical thinking individuals. Just remember, it is all color of law, technically a form of entrapment. Eventually they will tighten the noose, and cut everyone off from independent options altogether. In order to attain an education, in order to maintain a job, in order to enter a hospital or clinic, in order to go shopping, in order to travel, in order to live amongst others (including your family) within any community, ultimately in order to function on any practical level within society, you will be FORCED to get your shots.

Mandatory vaccinations are being phased in incrementally, by stealth, through this co-ordinated, systemic process of passive aquiescence. Once the “cashless grid” police state infrastructure is firmly in place, worldwide, EVERY citizen (excluding those Elites who manage the populace from on high), will be forced to submit to all standard immunization protocols by LAW (including Government/CDC issued “pandemic shots” inevitably designed to sterilize the host) on penalty of forfeiture/suspension of their vital carbon credit allotment. So it is now emcumbant upon you as an individual to decide the course of your future. Are you going to serve the corporation…and join the herd, or stand by your family? Think about it. VRM

Those doctors who endorse the continued use of Thimerosal in vaccines, including the authors of the recent American Academy of Pediatrics article here-in (Walter A. Orenstein, MD, Jerome A. Paulson, MD, FAAP, Michael T. Brady, MD, FAAP, Louis Z. Cooper, MD, Katherine Seib, MSPH), should have their licences revoked immediately. But it’s also time for conscientious parents to consider walking away, once & for all, from the ENTIRE institution of Western Allopathic Medicine; all the trappings of this Medical Mafia monopoly. You have the evidence in hand.  
‘Vaccines remain one of the most effective ways to prevent infectious disease and deaths globally. Universal childhood immunization provides herd immunity against many infectious agents and is a policy that has achieved dramatic reductions in common childhood illnesses. Overwhelmingly, the evidence collected over the past 15 years has failed to yield any evidence of significant harm, including serious neurodevelopmental disorders, from use of thimerosal in vaccines. Dozens of studies from countries around the world have supported the safety of thimerosal-containing vaccines. The preponderance of available evidence has failed to demonstrate serious harm associated with thimerosal in vaccines. As such, we extend our strongest support to the recent Strategic Advisory Group of Experts recommendations to retain the use of thimerosal in the global vaccine supply.’ American Academy of Pediatrics, 12/17/2012

Eli Lilly and Company: Thimerosal/Material Safety Data Sheet – ‘Thimerosal contains 49.6% w/w organically-bound mercury. Exposure Guidelines: Thimerosal – No known occupational exposure limits established. Early signs of mercury poisoning in adults are nervous system effects, including narrowing of the visual field and numbness in the extremities. Exposure to mercury in utero and in children may cause mild to severe mental retardation and mild to severe motor coordination impairment.’

A single thimerosal-containing vaccination produces acute ethylmercury blood levels of 10–30 nM (nanomolar concentration), and blood samples in 2-month-old infants, obtained 3–20 days after vaccination, contain 3.8–20.6 nM ethylmercury. Our studies therefore indicate the potential for thimerosal to cause adverse effects on MS (methionine synthase – determines the viability of cells) activity at concentrations well below the levels produced by individual thimerosal-containing  vaccines.’ M Waly, H Olteanu, R Banerjee, S-W Choi, JB Mason, BS Parker,  S Sukumar, S Shim, A Sharma, JM Benzecry, V-A Power-Charnitsky, RC Deth – See page 10


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.

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

Aluminum + Thimerosal = twice the toxic overload – ‘Mercury readily combines with aluminium to form a mercury-aluminium amalgam when the two pure metals come into contact. A small amount of mercury can “eat through” a large amount of aluminium over time, by progressively forming amalgam and relinquishing the aluminium as oxide.’ Whereas Aluminum is the more dominant metal as a coagulant & in terms of its net charge on the body, Mercury is clearly the more corrosive element.

A small dose of mercury that kills 1 in 100 rats and a dose of aluminum that will kill 1 in 100 rats, when combined have a striking effect: all the rats die. Doses of mercury that have a 1 percent mortality will have a 100 percent mortality rate if some aluminum is there.” Donald Miller, M.D. Professor of Surgery, University of Washington

See VRM: The Problem With Vaccines Part 2 – Synergistic Effect of Heavy Metal Toxicity On The Body


Christmas message from the Vaccine Resistance Movement


Based on all my research into the mainstream Medical Mafia, I have come away with one prevailing conclusion: The whole foundation on which symptom-based Allopathic Medicine is built runs counter to the holistic principles of the human body, a medieval construct which has been undermining natural immunity since its inception in the early 19th Century; unleashing a cat’s cradle of hybrid cancers on our communities at large. Our children have also become breeding grounds for laboratory produced pathogens, bacterium & rogue, weaponized viruses.

The advent of “Herd Immunity” has done more to damage “natural” immunity than any plague or war experienced through the history of civilization. The entire methodology behind vaccines, including the manufacturing process itself, is rife with problems. We have become nothing more than statistics on a graph, vessels in a multi-billion dollar Industry out of control; one beholden to its own relentless greed. We were never meant to die so young nor suffer the litany of infections, disorders & diseases now plaguing our lives.

The Medical Establishment clearly values profit-making over enhancing the quality & longevity of life. Our Governments have seen fit to broker secret, binding deals with the UN/WHO & Vaccine Manufacturers, to the detriment of our safety & inherent, natural-born rights. We are seemingly headed toward a nightmare scenario, soon to be stripped of our fundamental privilege to choose, to determine for ourselves & our families what goes into our bodies. The only hope is to make it our primary goal to secure forever our sacred rights to self-determination of the body. This will depend on us taking a stand against whichever form of tyranny that threatens these fundamental, natural born, freedoms.  

The transition to self-sufficiency, in terms of restoring optimal natural health in the body, requires a genuine paradigm shift in consciousness AWAY from dependency on outside forces, by reclaiming the inherent instinct for survival and unregulated communal living; where-in we can relearn the wisdom & knowledge of natural cures (via tinctures, broths, ointments, spices, essential oils, phytonutrient & antioxidant derived holistic remedies) which our ancestors coveted and passed on from generation to generation within the community.

The path to self-determination of the body MUST be taken alone. In order to discover your own inherent strength of will, the ability to see past all the lies & propaganda that have been foisted upon you and those around you (by those chosen Elites in positions of high power who seek to control you) for generations, you must walk that solo path up the proverbial mountain, to gradually unfurl the damage done to your capacity for natural immunity and genuine unregulated free-will. Only by facing your fears and self-doubt ALONE can you attain that strength within your heart to stand free from tyranny. This is key to self-empowerment. Those who have sought to keep you in bondage since civilization has existed, know this to be true. And they fear your strength, as they turn away from their own capacity for humanity.

I am now convinced that there is but one path out of the mess created by Western Allopathic Medicine and all its hazards & mistakes: Just walk away. What I am advocating is making a clean break, by completely divorcing yourself from all their rhetoric, all the toxic products that are peddled in the name of mainstream medicine, and returning to that sacred path on which our ancestors still stand. Their knowledge is your strength. You certainly won’t regret it. Merry Christmas, one & all, from the Vaccine Resistance Movement




I find it ironic that my work on vaccines receives the most criticism & scepticism from those mainstream medical professionals (fresh out of Medical school) working on the front lines. The vast majority of parents I encounter, however, particularly those with children suffering from neurological & neurodevelopmental difficulties, are able to grasp the evidence I lay out before them without prejudice; avoiding the trap common amongst those trained in the halls of Western Allopathic Medicine, that of consciously obstructing one’s capacity for critical thinking, when the truth flies in the face of everything you were taught to believe, everything you have invested in.

Typically, graduate level Medical students are the most arrogant in their newfound position & overall understanding of natural health, likewise the most vocal toward those who oppose their ingrained viewpoints; where-as veteran mainstream doctors on the front lines tend to withdraw from all such discussions, avoiding unnecessary controversy, choosing instead to rely on Medical seminar data & the omnipotent Big Pharma supply line to justify their actions visa vi promoting vaccine uptake. VRM


Generation RX

In the aftermath of the devastating tragedy in Newtown, Connecticut, this is clearly a time for heart-felt grieving and close family reflection. However, it is still CRITICALLY important to note that the shooter, Adam Lanza, was diagnozed with Asperger Syndrome, a higher functioning form of Autism, which manifests in delayed social & motor skills, plus extreme sensitivity to sensory stimuli (a commonality of symptoms with those children coping with severe forms of Autism ie. identical dietary deficiencies).

The Mayo Clinic routinely recommends the use of anti-depressants & anti-psychotic drugs (Selective Serotonin Re-uptake Inhibitors) for Autism related “symptom management”. It will undoubtedly surface in the coming days & weeks, that Adam Lanza had been prescribed “Antipsychotic medication” such as thioridazine (Mellaril), haloperidol (Haldol), chlorpromazine (Thorazine), clozapine (Clozaril), sertindole (Serlect), olanzapine (Zyprexa), or risperidone (Risperdal), and/or in combination with anti-depressants (Paxil, Prozac, Luvox, Seroxat, Celexa, Lexapro, Cipralex, Zoloft, Lustral, Dilantin, Coumadin) – all of which are ADMITTED to cause psychotic breaks and suicidal-type tendancies in those suggestible/susceptible to inwardly-outwardly destructive thought patterns, particularly in children/teens already close to the edge.

This demonstrates a fundamental lack of understanding of synergistic toxicity, and a clear disconnect between University & Hospital backed Scientific Research divisions and those Medical practitioners working on the front lines – since it has been proven that ALL anti-psychotic drugs have a devastating impact on the Autistic condition, when administered to children to with advanced/severe Autism – linked to a cascading neuro-developmental syndrome known as Tardive Dyskinesia…’characterized by repetitive, involuntary, purposeless movements. Features of the disorder may include grimacing, tongue protrusion, lip smacking, puckering & pursing, rapid eye blinking. Rapid movements of the arms, legs, trunk may also occur.’

In this case, Adam Lanza felt increasingly isolated within his community, despite his mother’s apparent devotion to him, had withdrawn from those capable of addresing his needs on all fronts, and either could not reach out for or refused support, hindered by his Asperger’s condition – which was undoubtedly exaserbated by years of exposure to prescription anti-depressants & anti-psychotic drugs – fed into by a video-game culture which promotes irrational violence and self-loathing. My point is, this individual was not a monster by nature. And the fact that he had access to guns is not the root of the problem. My heart weeps for all these beautiful children and adults whose lives have been cut short so violently. Perhaps now we can dig deeper, to ensure our children aren’t led down the same distorted path, that ultimately love and family will endure and ENSURE that such attrocious acts never see the light of day again. VRM

See GENERATION RX by Kevin Miller – exposes the scam behind Prescription Drugs, the deliberate chemical lobotomizing of an entire generation for profits & societal degeneration


There are some issues which supercede job security. This is one of them. It’s time for Health Care Workers everywhere to stand up for their basic rights to self-determination of the body, with a blanket refusal of all draconian workplace vaccine mandates. If that means losing your current job in the bargain, then it is a short term sacrifice worth making. There will always be viable employment opportunities available throughout the alternate sector of clinics, hospitals & private practices.

Once you give in to increasingly stringent authoritarian measures, you risk not only your immediate & longterm health, but, in doing so, will thus have abdicated your inherent freedom to choose as an individual, and sacrificed your professional integrity to a misguided & scientifically invalid policy directive. A growing number of families throughout our community have reached the same conclusion: The Flu Vaccine is a complete, abject fraud & failure. Stand firm in your belief, as many others have. You are all truly an inspiration to your colleagues!

Cincinnati ‘Health system TriHealth’, a centralized health care system controller which operates Good Samaritan & Bethesda North hospitals, Hospice of Cincinnati, Queen City Physicians & Group Health Associates doctors groups, is set to fire 150 front line Health Care Worker “employees” on Wednesday, November 29th. All received termination notices the day before Thanksgiving, for failing to comply with a mandatory Flu shot regulation.

Note: ‘They have until December 3rd to acquiesce or face “termination”.

‘Health system TriHealth had a message for 150 employees Wednesday: We really mean it this time. The 150 workers who didn’t get the required flu shots by the Nov. 16 deadline received termination notices the day before Thanksgiving. To keep their jobs, they need a flu shot by Dec. 3 (2012). “The flu vaccine still is the best way to protect our employees and our patients against the flu,” spokesman Joe Kelley said.

TriHealth required all 10,800 employees to get flu shots. This is the third year it’s issued terminations for failure to get vaccinations. It has offered the shots for free since Oct. 1 and will continue to offer them through Dec. 3. Several of the region’s biggest health systems also require flu shots. Insurers and employers often recommend them to fight off the flu, but health systems are increasingly adamant in an effort to protect patients. Some have gone even further. Cincinnati Children’s Hospital Medical Center in previous years has restricted access to patient rooms for everyone except families during flu season.’

Eight Indiana front-line nurses, most of them veterans with decades of experience, have been fired outright for refusing to take the Flu shot. Religious exemption waivers were overlooked.

‘An Indiana hospital has fired eight employees, many of them veteran nurses, because they refused to take the flu vaccine. IU Health Goshen is just the latest hospital to force its employees to receive the jab and fire or discipline the ones who object. At least four of the nurses who was terminated tried to appeal the vaccine on religious grounds with the help of a lawyer. The hospital rejected their arguments and fired them anyway.

‘I feel like in my personal faith walk, I have felt instructed not to get a flu vaccination, but it’s also the whole matter of the right to choose what I put in my body and what I feel God wants me to put in versus someone mandating what I put in,’ Joyce Gingerich told the Truth. Ms Gingerich, an oncology nurse who worked at the hospital in Goshen for 25 years, said she didn’t want to leave her patients or her job – but she said she couldn’t compromise her religious beliefs. Sue Schrock, a hospice nurse, said she has not had a flu vaccine for 30 years as a result of a choice she made because of her Christian faith. She said compromising that position was unthinkable.’


The Tamiflu Deception

Roche Pharmaceuticals, manufacturer of Tamiflu (oseltamivir phosphate) – marketed as ‘a prescription drug…an oral antiviral treatment (not a vaccine!) for influenza, belong(ing) to a class of medicines called neuraminidase inhibitors (NAI) ostensibly designed to be active against all clinically relevant influenza virus strains…proven to be effective in the treatment and for the prevention of influenza in adults and in children 1 year and older’, are currently facing intense scrutiny in Medical circles, for deliberately withholding primary Clinical Trial data on Tamiflu. Under pressure from a UK Government led commission investigating the safety & efficacy of neuraminidase inhibitors, the British Medical Journal (BMJ), backed by the Cochrane Collaboration (a non-profit international organization comprised of the world’s leading Medical researchers & practitioners) have jointly accused Roche of deliberately withholding the majority of “full study reports” pertaining to the anti-viral drug Tamiflu, including suppressing potentially damning evidence of adverse side effects.

‘8 of the 10 RCT’s (randomized controlled trials), on which effectivcness claims (of Tamiflu) were based, were never published, and the only 2 that had been published were funded by Roche and authored by Roche employees and Roche-paid external experts…The Cochrane reviewers now know that there are at least 123 trials of Tamilfu and that the majority (60%) of patient data from Roche Phase 3 completed treatment trials remains unpublished. There are concerns on a number of fronts: the likely overstating of effectiveness and the apparent under-reporting of potentially serious adverse effects.

Tamiflu has been a great commercial success for Roche. Billions of pounds of public money have been spent on it, and yet the evidence on its effectiveness and safety remains hidden from appropriate nad necessary independent scrutiny. I am appealing to you as an internationally respected scientist and clinician and a leader of clinical research in the UK to bring your influence to bear on your colleagues on Roche’s board. As company directors, responsibility for Roche’s behavior rests with you, both as individuals and colllectively. In refusing to release these data of enormous public interest, you put Roche outside the circle of responsible pharmaceutical companies.’ Fiona Godlee, Editor-in chief of the British Medical Journal (BMJ), October 2012

Peter Gøtzsche, head of the Nordic Cochrane Centre in Copenhagen, has called for a unilateral boycott on all Roche produced products until they comply with a formal full disclosure policy on Tamiflu. “Roche has withheld data that purports to show that Tamiflu has dramatic effects. We all wonder why it is so difficult to get these data from Roche and why Roche has not published them if it is really true that they show these effects. European governments should sue Roche, which might have the effect that the hidden trial results come out in the open. Furthermore, I suggest we boycott Roche’s products until they publish missing Tamiflu data.

DESCRIPTION: TAMIFLU (oseltamivir phosphate) is available as capsules containing 30 mg, 45 mg, or 75 mg oseltamivir for oral use, in the form of oseltamivir phosphate, and as a powder for oral suspension, which when constituted with water as directed contains 12 mg/mL oseltamivir base. In addition to the active ingredient, each capsule contains pregelatinized starch, talc, povidone K 30, croscarmellose sodium, and sodium stearyl fumarate. The 30 mg capsule shell contains gelatin, titanium dioxide, yellow iron oxide, and red iron oxide. The 45 mg capsule shell contains gelatin, titanium dioxide, and black iron oxide. The 75 mg capsule shell contains gelatin, titanium dioxide, yellow iron oxide, black iron oxide, and red iron oxide. Each capsule is printed with blue ink, which includes FD&C Blue No. 2 as the colorant. In addition to the active ingredient, the powder for oral suspension contains sorbitol, monosodium citrate, xanthan gum, titanium dioxide, tutti-frutti flavoring, sodium benzoate, and saccharin sodium.

Oseltamivir phosphate is a white crystalline solid with the chemical name (3R,4R,5S)-4-acetylamino- 5-amino-3(1-ethylpropoxy)-1-cyclohexene-1-carboxylic acid, ethyl ester, phosphate (1:1). The chemical formula is C16H28N2O4 (free base).

In clinical studies in the treatment of naturally acquired infection with influenza virus, 1.3% (4/301) of posttreatment isolates in adult patients and adolescents, and 8.6% (9/105) in pediatric patients aged 1 to 12 years showed emergence of influenza variants with decreased neuraminidase susceptibility in cell culture to oseltamivir carboxylate. Substitutions in influenza A neuraminidase resulting in decreased susceptibility were H274Y in neuraminidase N1 and E119V and R292K in neuraminidase N2.

In clinical studies of postexposure and seasonal prophylaxis, determination of resistance by population nucleotide sequence analysis was limited by the low overall incidence rate of influenza infection and prophylactic effect of TAMIFLU.

Note: ‘Insufficient information is available to fully characterize the risk of emergence of TAMIFLU resistance in clinical use.’

Disclaimer: ‘People with the flu, particularly children and adolescents, may be at an increased risk of seizures, confusion, or abnormal behavior early during their illness. These events may occur shortly after beginning TAMIFLU or may occur when flu is not treated. These events are uncommon but may result in accidental injury to the patient. Therefore, patients should be observed for signs of unusual behavior and a healthcare professional should be contacted immediately if the patient shows any signs of unusual behavior.

It is important that you begin your treatment with TAMIFLU as soon as possible from the first appearance of your flu symptoms or soon after you are exposed to the flu. If you feel worse or develop new symptoms during treatment with TAMIFLU, or if your flu symptoms do not start to get better, you should contact your healthcare professional.

If you have the flu: Take TAMIFLU twice a day for 5 days, once in the morning and once in the evening. You should complete the entire treatment of 10 doses (capsules or suspension), even if you feel better.’

‘Observed During Clinical Practice: The following adverse reactions have been identified during postmarketing use of TAMIFLU. Because these reactions are reported voluntarily from a population of uncertain size, it is not possible to reliably estimate their frequency or establish a causal relationship to TAMIFLU exposure.
Body as a Whole: Swelling of the face or tongue, allergy, anaphylactic/anaphylactoid reactions
Dermatologic: Dermatitis, rash, eczema, urticaria, erythema multiforme, Stevens-Johnson Syndrome, toxic epidermal necrolysis (see PRECAUTIONS)
Digestive: Hepatitis, liver function tests abnormal
Cardiac: Arrhythmia
Gastrointestinal disorders: Gastrointestinal bleeding, hemorrhagic colitis
Neurologic: Seizure
Metabolic: Aggravation of diabetes
Psychiatric: Delirium, including symptoms such as altered level of consciousness, confusion, abnormal behavior, delusions, hallucinations, agitation, anxiety, nightmares’

In a 2-week study in unweaned rats, administration of a single dose of 1000 mg/kg oseltamivir phosphate to 7-day-old rats resulted in deaths associated with unusually high exposure to the prodrug. However, at 2000 mg/kg, there were no deaths or other significant effects in 14-day-old unweaned rats. Further follow-up investigations of the unexpected deaths of 7-day-old rats at 1000 mg/kg revealed that the concentrations of the prodrug in the brains were approximately 1500-fold those of the brains of adult rats administered the same oral dose of 1000 mg/kg, and those of the active metabolite were approximately 3-fold higher. Plasma levels of the prodrug were 10-fold higher in 7-day-old rats as compared with adult rats. These observations suggest that the levels of oseltamivir in the brains of rats decrease with increasing age and most likely reflect the maturation stage of the blood-brain barrier. No adverse effects occurred at 500 mg/kg/day administered to 7- to 21-day-old rats. At this dosage, the exposure to prodrug was approximately 800-fold the exposure expected in a 1-year-old child.

The concurrent use of TAMIFLU with live attenuated influenza vaccine (LAIV) intranasal has not been evaluated. However, because of the potential for interference between these products, LAIV should not be administered within 2 weeks before or 48 hours after administration of TAMIFLU, unless medically indicated. The concern about possible interference arises from the potential for antiviral drugs to inhibit replication of live vaccine virus. Trivalent inactivated influenza vaccine can be administered at any time relative to use of TAMIFLU.

Note: ‘No influenza vaccine interaction study has been conducted.’ Roche Pharmaceuticals
There is compelling evidence that the routine administering of post Influenza vaccination Prescription Drugs (Vancomycin & Oseltamivir aka Tamiflu) not only hastened the critical conditions of those who sought hospital care, but may, in fact, have triggered the premature deaths of most, if not all children who succumbed to 2009’s laboratory produced “novel” strain of H1N1 (2 parts Swine Flu, 1 part Human Flu, 1 part Avian Flu).

‘While most of the children critically ill with H1N1 had one or more chronic health conditions that increased their risk, such as asthma, neurologic disorders or compromised immune systems, 251 children (30 percent) were previously healthy. Among these otherwise healthy children, the only risk factor that was identified for death from influenza was a presumed diagnosis of MRSA co-infection in the lung – which increased the risk for mortality 8-fold (P<0.0001). 88 percent of the children admitted to the ICU received Tamiflu (oseltamivir) during their stay, but only 6 percent had received it prior to hospital    admission…The study also found that most of the MRSA co-infected children who died had received vancomycin promptly at or before ICU admission.’ Children’s Hospital, Boston

Note: ‘88 percent of the children admitted to the ICU received Tamiflu (oseltamivir) during their stay…’

Tamiflu under examination – Side Effects: ‘Allergic reactions sometimes leading to shock, Asthma, Bronchitis, Chest   infection, Conjunctivitis, Dermatitis, Diarrhoea, Difficulty sleeping,   Dizziness, Ear infection, Ear problems, Erythema multiforme, Headache, Hepatitis, Indigestion, Liver problems, Lymphadenopathy, Nausea, Nose   bleed, Rash or rashes, Runny nose, Sinusitis, Stevens Johnson syndrome,   Urticaria, Vomiting.

A teenage girl left disabled by the swine flu treatment Tamiflu did not   even have the virus, it was revealed today. Samantha Millard, 19,  became  critically ill after suffering a severe allergic reaction to the   tablets, which she took on the advice of the controversial NHS  helpline. Within 72 hours of taking three pills, doctors put her on  life support.

Note: ‘..became critically ill after suffering a severe allergic reaction to the tablets (Tamiflu)…Within 72 hours of taking three pills, doctors put her on life support.’

‘The detection of an increased number of A(H1N1) viruses with resistance to oseltamivir (Tamiflu)  was initially reported to WHO by Norway on 25 January 2008. The  viruses carried a specific neuraminidase (NA) mutation (H274Y) that confers high-level resistance to oseltamivir in N1-containing influenza viruses. Prior to the recent report from Norway, such resistance was rarely observed in community isolates of influenza A or B. During the previous northern hemisphere winter season (2006/2007), surveillance through the Global Influenza Surveillance Network (GISN) laboratories found no oseltamivir-resistant H1N1 viruses among isolates from Japan  or Europe, and less than 1% prevalence among H1N1 isolates from the United States of America.

The mutation in N1 neuraminidase of human influenza virus which confers high-level resistant to oseltamivir is a single amino acid substitution of the relevant histidine (H) to   tyrosine (Y) at position 275. Most of the early work on structure and   inhibitor design is based on two other subtypes (N2 and N9) and the   corresponding amino acid in these subtypes is at position 274. Consequently, some scientists use ‘N2 numbering’ (H274Y) and some use the actual ‘N1 numbering’ (H275Y).’ WHO

Note: ‘…detection of an increased number of A(H1N1) viruses with resistance to oseltamivir (Tamiflu)…high-level resistance to oseltamivir in N1-containing influenza viruses

Preliminary data from the early 2008-2009 influenza season indicates that oseltamivir (Tamiflu) resistance among A(H1N1) viruses continues at high levels. As of February 19, 2009, resistance to oseltamivir had been identified among 264 of 268 (98.5 percent) U.S. influenza A(H1N1) viruses tested. “The emergence of oseltamivir resistance has highlighted the need for the development of new antiviral drugs and rapid diagnostic tests that determine viral subtype or resistance, as well as improved representativeness and timeliness of national influenza surveillance for antiviral resistance.”‘ Journal of The American Medical Association (Jama)/2009

Note: ‘As of February 19, 2009, resistance to oseltamivir (Tamiflu) had been identified among 264 of 268 (98.5 percent) U.S. influenza A(H1N1) viruses tested.’

Scientists on the Tamiflu (manufactured by Roche) double dipping payroll include:

1. Dr.René Snacken/Belgian Ministry of Public Health, WHO Division of Viral Diseases (1998), Co-author of ‘Influenza Pandemic Plan: The Role of WHO and Guidelines for National and Regional Planning’ (1999), also funded researcher for Roche (Tamiflu).

2. Dr Daniel Lavanchy/Co-author of ‘Influenza Pandemic Plan: The Role of WHO and Guidelines for National and Regional Planning’ (1999),  appeared at a Roche sponsored symposium in 1998 while employed at WHO Division of Viral Diseases.

3. Professor Karl Nicholson/Leicester University, UK, Member of The European Scientific Working Group on Influenza (ESWI) which collaborated with WHO on ‘Influenza Pandemic Plan: The Role of WHO and Guidelines for National and Regional Planning’, also conducted a randomised controlled trial on oseltamivir (Tamiflu) supported by Roche.

4. Professor Abe Osterhaus/Erasmus University, Netherlands, Member of The European Scientific Working Group on Influenza (ESWI) which collaborated with WHO on ‘Influenza Pandemic Plan: The Role of WHO and Guidelines for National and Regional Planning’, also conducted a randomised controlled trial on oseltamivir (Tamiflu) supported by Roche.

Vancomycin under examination: ‘Treatment failures of vancomycin in patients with MRSA infections have been reported despite in vitro susceptibility. These failures have led to the utilization of vancomycin doses higher than those approved by the FDA. Higher doses are being administered to achieve goal vancomycin trough concentrations of 10-20 μg/mL recommended by several Infectious Diseases Society of America (IDSA) endorsed clinical practice guidelines. Recent studies suggest that increased rates of nephrotoxicity are associated with aggressive vancomycin dosing. These increased rates are confounded by concomitant nephrotoxins, renal insufficiency, and/or changing hemodynamics.’

Note: ‘Three published studies have suggested that there is a significant association between increased vancomycin through concentrations and nephrotoxicity (the quality of being destructive to kidney cells).’

There’s more risk for MRSA (methicillin-resistant Staphylococcus aureus) to become invasive in the presence of flu or other viruses.‘ How is that possible, a convergence of bacterial & viral infections, when it is common knowledge in medical circles that Influenza manifests independently as ‘an acute viral infection caused by an influenza virus‘, contrary to a ‘pathogenic infectious bacteria‘ capable of reproducing quickly & spreading infectious diseases in the body? The truth is the body is being systematically targeted & broken down from all sides, creating a perfect storm of toxicity which has derailed the inherent functionality of our natural immunity generation to generation; thereby opening the door to widespread ill health. Western medicine, however they spin its so called “progress”, continually offers the antithesis of a natural solution.

‘There have been many new developments in vaccine technology. Moreover, work on viral neuraminidase has led to the licensing of potent selective antiviral drugs, and economic decision modelling provides further justification for annual vaccination and a framework for the use of neuraminidase inhibitors. Progress has also been made on developing near-patient testing for influenza that may assist individual diagnosis or the recognition of widespread virus circulation, and so optimise clinical management. Despite these advances, the occurrence of avian H5N1, H9N2, and H7N7 influenza in human beings and the rapid global spread of severe acute respiratory syndrome are reminders of our vulnerability to an emerging pandemic.

The contrast between recent cases of H5N1 infection, associated with high mortality, and the typically mild, self-limiting nature of human infections with avian H7N7 and H9N2 influenza shows the gaps in our understanding of molecular correlates of pathogenicity and underlines the need for continuing international research into pandemic influenza. Improvements in animal and human surveillance, new approaches to vaccination, and increasing use of vaccines and antiviral drugs to combat annual influenza outbreaks are essential to reduce the global toll of pandemic and interpandemic influenza.’ Infectious Diseases Unit, Leicester Royal Infirmary, Leicester, UK

The routine administering of post Influenza vaccination Prescription Drugs  (Vancomycin & Oseltamivir aka Tamiflu) led to serious adverse interactions which not only hastened the critical conditions of those  who sought hospital care, but may, in fact, have triggered the premature deaths of most, if not all children who succumbed to 2009’s laboratory  produced “novel” strain of H1N1 (2 parts Swine Flu, 1 part Human Flu, 1  part Avian Flu).

The truth is the body is being systematically targeted & broken down from all sides, creating a perfect storm of toxicity  which has derailed the inherent functionality of our natural immunity generation to generation; thereby opening the door to widespread ill  health. Western medicine, however they spin its so called “progress”, continually offers the antithesis of a natural solution.

It is no longer a coincidence to suggest a correlation between “natural vs. manufactured (prescription)” anti-biotic/anti-viral   breakdown in the body and “natural vs manufactured (prescription)” anti-biotic/anti-viral resistance overload proliferating in the environment. Approximately ‘2 out of every 100 people carry a strain of staph that is resistant to these antibiotics‘. We have reached the saturation point as a species; with the continued oversight of Western Allopathic Medicine, focusing solely on treating (and thereby exacerbating) symptoms rather than seeking out & remedying (embracing) the underlying cause.

See VRM: The Flu Report

See: VRM: PCV Vaccine Exposed – Breeding Ground For Staphylococcus Aureus


BC Nurses’ Union & British Medical Doctor unite in opposition to Government Health directive demanding mandatory Flu shot for front line Health care workers – issue a “formal grievance” in opposition to the “coersive” & “tyrannical” tactics, citing lack of credible scientific evidence

‘Another round of fighting has erupted between British Columbia’s nurses and its health officer after a U.K.-based, non-profit scientific group publicly questioned the evidence used to justify a mandatory flu-shot policy for provincial health-care workers. Citing a letter in a Vancouver newspaper written by a doctor associated with group known as the Cochrane Collaboration, the BC Nurses’ Union announced Wednesday it has launched a formal grievance over the policy, while also demanding its immediate withdrawal.

But Dr. Perry Kendall, B.C.’s health officer, said he thinks members of the public will be left scratching their heads over the science and called the nurses’ action “undermining.” This past August, Kendall announced the policy that requires health-care workers to get a flu shot or wear masks during the flu season. Union officials say those who are vaccinated are expected to wear a distinctive badge indicating they’ve had the shot.


“We’re going to base our practice on the best science,” said Debra McPherson, president of the nurses’ union. “Getting an immunization, getting a foreign body shot into your body, should be a matter of choice. Certainly for health-care workers where the science is not compelling, it should continue to be their choice and they shouldn’t be coerced or punished for choosing, based on their reading of the science, to not get it.”

In the letter published in The Vancouver Sun, Dr. Tom Jefferson of the Cochrane Collaboration said Kendall misquoted a 2010 review conducted by his organization, when the health officer justified the vaccination of employees as a way to protect patients from the flu and pneumonia. Jefferson said the Cochrane Collaboration drew no such conclusion. “In other words, we report that no effect of the influenza vaccines was detectable on influenza and its complications such as death,” he wrote. He ended the letter with some strong words. “It is not my place to judge the policies underway in British Columbia, but coercion and forcing public ridicule on human beings (for example by forcing them to wear distinctive badges or clothing) is usually the practice of tyrants,” wrote Jefferson.

The union seized on the opinion and said in a release it “shredded” the rationale behind the policy. McPherson said in a followup interview that her union has now corresponded with the CEO of Health Employers Association of BC and demanded it step back from the policy. “If the science isn’t there, how can the employer bring into place a coercive and punitive policy which has people wearing badges indicating whether or not they’ve been vaccinated for the flu,” she said.

But Kendall pointed to several medical journals that he said promote similar policies. “The Lancet, the British Medical Journal, the Canadian Medical Association Journal, the Society for Healthcare Epidemiology in the United States, they’ve all called for mandatory immunization of health-care workers.”  He said even though the vaccination isn’t as effective as medical officials originally thought, it’s still about 60 per cent effective, which considerably reduces the chances somebody will pick up the virus and pass it on to patients. When asked how many patients die each year because they pick up viruses like the flu, Kendall said he didn’t know because the information is not routinely collected. He even acknowledged the public could be confused by the fight between the nurses and province. “If I was a member of the public, I’d be scratching my head because it certainly seems very undermining,” he said.’


Note: “We’re going to base our practice on the best science. Getting an immunization, getting a foreign body shot into your body, should be a matter of choice. Certainly for health-care workers where the science is not compelling, it should continue to be their choice and they shouldn’t be coerced or punished for choosing, based on their reading of the science, to not get it. If the science isn’t there, how can the employer bring into place a coercive and punitive policy which has people wearing badges indicating whether or not they’ve been vaccinated for the flu?” Debra McPherson, president of the BC Nurses’ union

Note: “We report that no effect of the influenza vaccines was detectable on influenza and its complications such as death. It is not my place to judge the policies underway in British Columbia, but coercion and forcing public ridicule on human beings (for example by forcing them to wear distinctive badges or clothing) is usually the practice of tyrants.” Dr. Tom Jefferson of the Cochrane Collaboration

UPDATE: A stay of execution, or more precisely, a major victory is unfolding, as health-care workers in British Columbia, Canada, have been “temporarily” granted the right to refuse workplace sanctioned mandatory vaccinations. The momentum generated by this local resistance to tyranny will inspire other nurses & doctors around the world facing similar demands to defend their inherent right to self-determination of the body. VRM
‘The B.C. government has temporarily backed away from a controversial plan to force thousands of provincial health workers to get a flu shot before they can work with patients. Instead of forcing workers to wear a mask or have the mandatory flu vaccination, the B.C. Health Ministry said it will work towards compliance from workers in the first year of the program. In a letter dated Nov. 30 to B.C.’s health authority chief executive officers, deputy health minister Graham Whitmarsh said components of the influenza control policy would not be enforced for the first year. The policy remains in effect, but no disciplinary measures will be taken, a ministry official explained. “I would like to afford health care workers the additional opportunity to voice their opinions on how best to achieve our shared objective,” his letter said.

The government launched the mandatory program to protect patients because it said a voluntary plan wasn’t working. Fewer than 50 per cent of workers were being vaccinated against the flu in some health settings.

The B.C. Nurses Union said it also welcomes the decision by government. “Given the clearly conflicting evidence about the effectiveness of the (flu) shot, we were very much opposed to policies aimed at forcing workers to get it,” Debra McPherson, union president, said in a statement. She said her union is more than willing to work with employers and the Health Ministry over the issue. “It has always been about education, not punishment.”‘

Vaccines for preventing influenza in healthy adults: ‘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.This review includes 15 out of 36 trials funded by industry (four had no funding declaration). An earlier systematic review of 274 influenza vaccine studies published up to 2007 found industry funded studies were published in more prestigious journals and cited more than other studies independently from methodological quality and size. Studies funded from public sources were significantly less likely to report conclusions favorable to the vaccines. The review showed that reliable evidence on influenza vaccines is thin but there is evidence of widespread manipulation of conclusions and spurious notoriety of the studies. The content and conclusions of this review should be interpreted in light of this finding.  

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.  

Authors of this review assessed all trials that compared vaccinated people with unvaccinated people. The combined results of these trials showed that under ideal conditions (vaccine completely matching circulating viral configuration) 33 healthy adults need to be vaccinated to avoid one set of influenza symptoms. In average conditions (partially matching vaccine) 100 people need to be vaccinated to avoid one set of influenza symptoms. Vaccine use did not affect the number of people hospitalised or working days lost but caused one case of Guillian-Barré syndrome (a major neurological condition leading to paralysis) for every one million vaccinations. Fifteen of the 36 trials were funded by vaccine companies and four had no funding declaration. Our results may be an optimistic estimate because company-sponsored influenza vaccines trials tend to produce results favorable to their products and some of the evidence comes from trials carried out in ideal viral circulation and matching conditions and because the harms evidence base is limited..’ Jefferson T, Rivetti A, Di Pietrantonj C, Demicheli V, Ferroni E, published in CochraneLibrary/2012  

Note: ‘There is no evidence that they (Influenza vaccines) affect complications, such as pneumonia, or transmission.’  

Note: ‘…reliable evidence on influenza vaccines is thin but there is evidence of widespread manipulation of conclusions and spurious notoriety of the studies…company-sponsored influenza vaccines trials tend to produce results favorable to their products.’  

Note: ‘At best, vaccines might be effective against only influenza A and B, which represent about 10% of all circulating viruses.’  

Vaccines for preventing influenza in healthy children (Review); ‘Inactivated vaccines in children aged two years or younger are not significantly more efficacious than placebo. Twenty-eight children over the age of six need to be vaccinated to prevent one case of influenza (infection and symptoms). Eight need to be vaccinated to prevent one case of influenza-like-illness (ILI). We could find no evidence of effect on secondary cases, lower respiratory tract disease, drug prescriptions, otitis media and its consequences and socioeconomic impact. We found weak single-study evidence of effect on school absenteeism by children and caring parents fromwork. Variability in study design and presentation of data was such that ameta-analysis of safety outcome data was not feasible. Extensive evidence of reporting bias of safety outcomes from trials of live attenuated influenza vaccines (LAIVs) impeded meaningful analysis. One specific brand of monovalent pandemic vaccine is associated with cataplexy and narcolepsy in children and there is sparse evidence of serious harms (such as febrile convulsions) in specific situations.’ Jefferson T, Rivetti A, Di Pietrantonj C, Demicheli V, Ferroni E, published in Cochrane Library/2012

Note: ”Inactivated vaccines in children aged two years or younger are not significantly more efficacious than placebo.’  

Note: ‘Extensive evidence of reporting bias of safety outcomes from trials of live attenuated influenza vaccines.’  

Note: ‘ pandemic vaccine is associated with cataplexy and narcolepsy in children.’

The Flu Vaccine deception ranks as one of the great cover-ups & swindles  of the last century perpetrated against the general population. Not only has the public been systematically lied to by their elected Gov’t for generations (in league with the World Health Organization & a Vaccine Industry Medical Mafia feeding trough), but the entire bedrock of our natural immunity has been put at risk through the collision of forces being pitted against us around the world.

The pattern emerging is clear, in terms of a criteria for determining the severity of seasonal Influenza – The majority of Flu deaths are attributed primarily to Bacterial Pneumonia triggered by the Flu symptoms. The Flu itself cannot kill you. Most victims of the Flu are those 65 years and older. In almost every instance a compromised immune system and/or a pre-existing medical condition is the key determinant factor in those unfortunate victims (at whichever age) who die from the Flu.

Further, most children who succumb to seasonal Flu, either via death or serious long-term illness (in particular those tracked since 2009), are subsequently found to have been 8 times more predisposed to a Methicillin-resistant Staphylococcus Aureus (MRSA) bacterial co-infection occurring in the lungs. It is also significant that routine prescription anti-bacterials/virals (chiefly Vancomycin Hydrochloride Capsules & Oseltamivir/Tamiflu), widely distributed globally to ostensibly combat flu-like symptoms, have in fact been the tipping point which has worsened such conditions, hastening Kidney failure, Myocarditis (inflammation of the Heart Muscle) & numerous instances of sudden death.

These are all critical factors, of which most families are currently unaware – due to a relentless Mainstream Media blackout on the truth & a vociferous Vaccine Lobby campaign meant to steer the “herd” into submission; while rapidly building up an Elitist Empire bent on eliminating the last vestiges of natural immunity which we still possess. The Flu Report aims to expose this global covenant of lies, while equipping you with the means of rebuilding your natural immunity, ultimately toward navigating your way out of this labyrinth once and for all.

See VRM: The Flu Report


Manufacturing giant ‘Novartis Vaccines’ is currently embroiled in a huge scandal involving Vaccine product contamination & formal misrepresentation of data – facing a widescale unilateral ban on all 2012/13 Novartis produced Influenza vaccines, after the discovery of “clumps” of “aggregate proteins” in numerous batches. The growing list of countries affected by the ban includes Switzerland, Italy, France, Germany, Austria & Canada

According to a Novartis spokesman, “The aggregate proteins are predominantly influenza virus-derived (mainly hemagglutinin), all normal and necessary components of influenza vaccines. Aggregation of these proteins is not unusual in vaccines manufacturing.”. ‘Protein aggregation can occur at all steps in the manufacturing process (cell culture, purification and formulation), storage, distribution and handling of products. It results from various kinds of stress such as agitation and exposure to extremes of pH, temperature, ionic strength, or various interfaces (e.g., air–liquid interface). High protein concentrations (as in the case of some monoclonal antibody formulations) can further increase likelihood of aggregation.’

‘Aggregation is a general term that encompasses several types of interactions or characteristics. Aggregates of proteins may arise from several mechanisms and may be classified in numerous ways, including soluble/insoluble, covalent/noncovalent, reversible/irreversible, and native/denatured. For protein therapeutics, the presence of aggregates of any type is typically considered to be undesirable because of the concern that the aggregates may lead to an immunogenic reaction (small aggregates) or may cause adverse events on administration (particulates).’

What Novartis has chosen not to reveal, and, in fact, gone to great lengths to conceal, is the patented formula they are utilizing for extraction, prolongation & PROLIFERATION of viral haemagglutinin (the protein on the outside of flu viruses that locks onto cells in the human respiratory tract to start the process of infection). Essentially, they have found a cost-effective means by which to rapidly replicate (through chemical synthesis of Influenza Virus proteins via Insect baculovirus protein carriers) & mass-produce Influenza Virus strains for use in assembly line production. ‘The antigens will typically be prepared from influenza virions (preferably grown in cell culture) but, in some embodiments, the antigens can be expressed in a recombinant host (e.g. in an insect cell line using a baculovirus vector). Chemical means for inactivating a virus include treatment with an effective amount of one or more of the following agents: detergents, formaldehyde, β-propiolactone, methylene blue, psoralen, carboxyfullerene (C60), binary ethylamine, acetyl ethyleneimine, or combinations thereof. Non-chemical methods of viral inactivation are known in the art, such as for example UV light or gamma irradiation.’ Novartis Vaccines & Diagnostics 
The “clumps” which have been discovered floating around in the Influenza Vaccine Vial serum are a composite of insect variety Baculovirus protein vectors & seasonal Influenza virus-derived protein vectors, laced with detergents, formaldehyde, β-propiolactone, methylene blue, psoralen, carboxyfullerene (C60), binary ethylamine, acetyl ethyleneimine and/or treated with UV light or gamma irradiation.
The Vaccine Resistance Movement recognizes the urgency of this matter, and will therefore be sending this unprecedented data, which exposes the methodology of systemic corruption rampant throughout the Vaccine Industry, to Government Health Departments around the world; in a concerted effort to warn the public, halt this wreckless method of production, begin immediate litigation proceedings against Novartis & further educate mainstream Medical practitioners on the front lines.
Novartis Package Insert – ‘AGRIPPAL S1 is an influenza vaccine. One dose (0.5 ml) contains: Active ingredients: Influenza virus surface antigens (haemagglutinin and neuraminidase), propagated in fertilized hen’s eggs from healthy chicken flocks, of the following strains:
1.A/California/07/2009 (H1N1) -like strain (A/California/07/2009, NYMC X-181) 15 micrograms HA*
2. A/Perth/16/2009 (H3N2) -like strain (A/Victoria/210/2009, NYMC X-187) 15 micrograms HA*
3. B/Brisbane/60/2008 – like strain (B/Brisbane/60/2008) 15 micrograms HA.
Excipients: sodium chloride; potassium chloride; potassium, dihydrogen phosphate; disodium phosphate dihydrate; magnesium chloride; calcium chloride and water for injection. The vaccine may contain residues of the following substances, e.g. eggs, chicken proteins, kanamycin and neomycin sulphate, formaldehyde, cetyltrimethylammonium bromide (CTAB) and polysorbate 80.’
Patent on use of Hemagglutinin protein vectors –  ‘Influenza Vaccines Containing Hemagglutinin and Matrix Proteins: The invention does not use a whole virion (WV) antigen i.e. it does not encompass vaccines that use a live virus or a whole inactivated virion. Instead, the antigens of the invention are non-WV antigens, such as split virions, or purified surface antigens. Compositions of the invention comprise at least two influenza virus antigens: haemagglutinin and matrix. They may also include other influenza virus antigen(s), such as neuraminidase. The antigens will typically be prepared from influenza virions (preferably grown in cell culture) but, in some embodiments, the antigens can be expressed in a recombinant host (e.g. in an insect cell line using a baculovirus vector) and used in purified form [3,4]. In general, however, antigens will be from virions. In preparing non-WV antigens from virions, virions may be inactivated.
‘Canada is following the lead of several European countries and suspending distribution of flu vaccine made by the pharmaceutical firm Novartis. The decision relates to the discovery by the company of tiny clumps of virus particles in some batches of flu vaccines made at the Novartis production facility in Italy. Novartis has agreed to suspend distribution of its vaccines – sold in Canada as Fluad and Agriflu – while the department investigates the situation. The department is also telling doctors and others who administer flu shots in Canada to hold off using the Novartis product for the time being. “We think it’s prudent, given the response of certain European countries to … request of Novartis – and they will be complying – to stop distributing and then to recommend to practitioners to refrain from using the (Novartis) vaccine just until this review is completed,” Dr. Paul Gully, senior medical advisory for Health Canada, said Friday.