{"id":13481,"date":"2014-04-07T05:36:34","date_gmt":"2014-04-07T13:36:34","guid":{"rendered":"http:\/\/vaccineresistancemovement.org\/?p=13481"},"modified":"2017-03-05T08:17:32","modified_gmt":"2017-03-05T16:17:32","slug":"vrm-the-measles-report","status":"publish","type":"post","link":"https:\/\/vaccineresistancemovement.org\/?p=13481","title":{"rendered":"VRM: Measles Report"},"content":{"rendered":"
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Do Vaccines actually confer immunity? Is Herd Immunity the stuff of science or myth? <\/span><\/strong>This Report explores the link between Vaccines, Herd Immunity & the current resurgence of Measles.\u00a0<\/span><\/strong><\/div>\n

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The\u00a0World Health Organization (WHO)\u00a0claims v<\/strong>accination programmes <\/strong>are m<\/strong>utually beneficial to all members within the community. B<\/strong>ased on <\/strong>th<\/strong>e her<\/strong>d immunity model, v<\/strong>accines n<\/strong>ot only<\/strong>\u00a0‘protect t<\/span><\/a><\/strong>he immunized, but can also reduce disease among unimmunized individuals in the community through \u201cindirect effects\u201d or \u201cherd protection\u201d…<\/span><\/a>‘<\/strong><\/p>\n

\u2018Herd protection\u201d of the unvaccinated occurs when a sufficient proportion of the group (95%) is immune. The coverage rate necessary to stop transmission depends on the basic reproduction number (R0), defined as the average number of transmissions expected from a single primary case introduced into a totally susceptible population. Diseases with high R0 (e.g. measles) require higher coverage to attain herd protection than a disease with a lower R0 (e.g. rubella, polio and Hib).<\/a>\u2019 Vaccination greatly reduces disease, disability, death and inequity worldwide\/WHO\u00a0\u00a0\u00a0 <\/strong><\/p>\n

By\u00a02020, the WHO a<\/strong>ims to achieve, globally,\u00a0‘at least 95% coverage with both the first and second routine doses of measles vaccine (or measles- rubella-containing vaccine as appropriate) in each district and nationally<\/span><\/a>.’<\/strong><\/p>\n

Notice that number, 95% vaccination rate, believed to be the tipping point which guarantees widespread \u2018herd immunity\u2019. Based on Vaccine methodology, the safety of the herd is predicated on the majority of the population, within the community (95%) getting vaccinated. Anything less, and the risk of viral transmission to the overall herd, by those still infected with Measles, theoretically, the unvaccinated population, remains high.<\/strong><\/p>\n

What exactly is Measles, and more importantly, why is it on the rise, once again in North America, spreading at such an alarming rate?<\/strong><\/p>\n

According to The Journal of Infectious Diseases<\/a>, Measles typically encompasses the following array of symptoms,<\/strong><\/p>\n

‘After an incubation period of 8\u201312 days, measles begins with increasing fever (to 39\u00b0C-40.5\u00b0C\/ or 104.9 degrees Fahrenheit) and cough, coryza, and conjunctivitis. Symptoms intensify over the 2\u20134 days before the onset of rash and peak on the first day of rash.<\/strong><\/p>\n

The rash is usually first noted on the face and neck, appearing as discrete erythematous patches 3\u20138 mm in diameter. The lesions increase in number for 2 or 3 days, especially on the trunk and the face, where they frequently become confluent. Discrete lesions are usually seen on the distal extremities, and with careful observation, small numbers of lesions can be found on the palms of 25%\u201350% of those infected. The rash lasts for 3\u20137 days and then fades in the same manner as it appeared, sometimes ending with a fine desquamation that may go unnoticed in children who are bathed daily.<\/strong><\/p>\n

An exaggerated desquamation is commonly seen in malnourished children. Fever usually persists for 2 or 3 days after the onset of the rash, and the cough may persist for as many as 10 days.<\/strong><\/p>\n

Measles virus infects multiple organ systems and targets epithelial, reticuloendothelial, and white blood cells, including monocytes, macrophages, and T lymphocytes.<\/strong><\/p>\n

Pathological studies of children dying during acute measles have found multinucleated giant cells typical of measles virus infection throughout the respiratory and gastrointestinal tracts and in most lymphoid tissues.<\/strong><\/p>\n

Measles virus infection leads to a decline in CD4 lymphocytes, starting before the onset of rash and lasting for up to 1 month, and resulting in suppression of delayed-type hypersensitivity as measured by anergy to skin test antigens, including tuberculosis antigen. Whether measles predisposes to reactivation of latent Mycobacterium tuberculosis infections has been a subject of debate.<\/strong><\/p>\n

Complications from measles have been reported in every organ system. Many of these complications are caused by disruption of epithelial surfaces and immunosuppression. Rates of complications from measles vary by age and underlying conditions.’<\/strong><\/p>\n

Measles related respiratory complications include:<\/strong><\/p>\n

1. Otitis media (middle ear inflammation\/bacterial infection).<\/strong><\/p>\n

2. Laryngotracheobronchitis (measles croup\/viral infection of the upper respiratory tract, causes varying degrees of airway obstruction).<\/strong><\/p>\n

3. ‘Giant cell’ Pneumonia (‘acute inflammation of the peri-bronchial lymphatics leading to a diffuse infiltration of the inter-alveolar connective tissue<\/span><\/a>‘) –\u00a0 associated with 80% of measles related fatalities. <\/strong><\/p>\n

Note: ‘Studies that included culture of blood, lung punctures, or tracheal aspirations revealed bacteria as the cause of 25%\u201335% of measles-associated pneumonia. S. pneumoniae, S. aureus, and H. influenzae were the most commonly isolated organ.<\/a>‘ <\/strong><\/p>\n

‘<\/strong>Pneumonia is the most common severe complication of measles and accounts for most measles-associated deaths. Laryngotracheobronchitis (is) the second most common cause of death in US children hospitalized with measles, after pneumonia<\/strong><\/span><\/a>….<\/strong>In recent years, pneumonia was present in 9% of children <5 years old with measles in the United States, in 0%\u20138% of cases during outbreaks, and in 49%\u201357% of adults<\/strong><\/span><\/a>.’ <\/strong><\/p>\n

‘<\/strong>The vast majority of serious complications associated with Measles (Death, Pneumonia, Encephalitis) are highest in children under 5.<\/strong><\/span><\/a>‘<\/strong><\/p>\n

‘<\/strong>Worldwide, there are estimated to be 20 million cases and 164,000 deaths each year. More than half of the deaths occur in India.<\/strong><\/span><\/a>‘ CDC<\/strong><\/p>\n

Note: \u2018Recent reports of increased S. aureus (Staphylococcus aureus \u2013 Hospital super bug)) colonization among children receiving pneumococcal vaccine implicate Streptococcus pneumoniae as an important competitor for the same niche.<\/a>‘\u2026‘a higher proportion of children with comorbidities had been previously vaccinated with >1 PCV7 (Pneumococcal Conjugate Vaccine) dose (22\/44 [50.0%] vs. 69\/204 [33.8%]).<\/a>\u2019<\/strong><\/p>\n

Whenever a child dies, in the days\/weeks\/months following vaccination, Medical authorities routinely obfuscate the evidence, shifting the blame AWAY from the Vaccine itself, to what is termed \u201ccomorbidities\u201d (pre-existing medical condition or complications inherent to that case-file \u2013 \u2018A concomitant but unrelated pathologic or disease process; usually used in epidemiology to indicate the coexistence of two or more disease processes.<\/a>\u2019).<\/strong><\/p>\n

The Vaccine Industry doesn\u2019t want you to know that vaccines cause the very signature disease\/disorder they claim to protect you against; albeit a more virulent \u201ctransforming\u201d strain of the primary pathogen.\u00a0 <\/strong><\/p>\n

SSPE (subacute sclerosing panencephalitis) is\u00a0‘a very rare, but fatal degenerative disease of the central nervous system that results from a measles virus infection acquired earlier in life. Analysis of data from an outbreak of measles in the United States during 1989-1991 suggests a rate of 4-11 cases of SSPE per 100,000 cases of measles. A risk factor for developing this disease is measles infection at an early age. Studies in the United Kingdom indicate that 18 out of every 100,000 people who get measles when they are less than a year old will develop SSPE. This is compared to 1.1 per 100,000 in those infected after 5 years of age. On average, the symptoms of SSPE begin 7 to 10 years after measles infection, but they can appear anytime from 1 month to 27 years after infection.<\/span><\/a>‘ CDC<\/strong><\/p>\n

Government Health Departments, backed by Mainstream Media outlets, are presently waging a witch-hunt against the unvaccinated, those among us who have taken an independent stance on vaccines, in a concerted effort to galvanize popular opinion, thereby boosting vaccination rates to meet their 95% mandate.\u00a0 <\/strong><\/p>\n

It is unscientific to single out a vaccine-free sector of the population as being responsible for spreading measles. The epicenters of Measles clusters typically intersect & overlap multiple local communities, ample opportunity for fully vaccinated individuals to intermingle with those unvaccinated individuals supposedly affected.\u00a0\u00a0 <\/strong><\/p>\n

Until the actual cases on the ground, are confirmed, meaning lab-verified, any such data (visa-vi daily bulletins) represents nothing more than a generalized estimate of actual numbers.<\/strong><\/p>\n

Yet again, the Media will undoubtedly be back-peddling 6 months from now, when the full extent of this outbreak, any such outbreak, is formally disclosed –\u00a0 as evidenced by the wave of retractions, following the debacle of the 2009 “Pandemic”. \u00a0 <\/strong><\/p>\n

Most so-called journalists are nothing more than propaganda peddlers & drug pushers for the Vaccine Industry, manipulating public opinion through fear-mongering headlines and deliberate misinformation.\u00a0<\/strong><\/p>\n

\u201c<\/strong><\/span>By the time all the dust has settled on H1N1, somewhere between 200 and 300 people will have died in this country. I\u2019m not letting the media off the hook totally, but I think the real villains of the piece here have been those public health officials who have consistently overplayed and overstated the importance of what is happening. By the time all is said and done, this is not a major public health event, but you\u2019d never know that from what some people are saying.<\/strong><\/span><\/a>\u201d Dr. Richard Schabas\/Chief Medical Officer of Health, Hastings & Prince Edward Counties, Ontario, Canada<\/strong><\/span><\/p>\n

‘The recent avalanche of belligerent media articles accompanied by the hostile tone of public commentaries implies that those who question vaccine theology are ignorant fanatics endangering the health and lives of children and the population as a whole. Acceptance of the vaccine agenda is so embedded in the public psyche that it has resulted in a mass paralysis of critical thinking skills absent any comprehension of the negative impact on health from artificial manipulation of the immune system.<\/span><\/a><\/strong><\/p>\n

The few reasoned voices who post comments are shouted down or are blocked from providing published evidence of vaccine risks, vaccine failures, outbreaks of disease in highly vaccinated populations, the vaccine injured, or the individual\u2019s right to vaccine choice. The atmosphere in mainstream media on this issue has disintegrated into an all out attack on anyone with an alternative view about vaccines.<\/span><\/a>‘ VRAN V-Bulletin<\/strong><\/p>\n

Even by Vaccine Industry standards, most mainstream doctors must acknowledge that vaccinated children are highly susceptible to viral shedding, for weeks, following vaccination; what the WHO refers to as direct\/indirect ‘person-to-person (horizontal) transmission’ <\/a>of a viral strain.\u00a0\u00a0 <\/strong><\/p>\n

This is particularly noteworthy in terms of the MMR Vaccine, which states, unequivocally, on the package insert, ‘M-M-R II has not been evaluated for carcinogenic or mutagenic potential, or potential to impair fertility.<\/a>\u2019<\/strong><\/p>\n

We have scientific verification of this trend on the ground.\u00a0Multiple recent peer-reviewed\u00a0sources have identified a distinct commonality associated with most Measles outbreaks,<\/strong><\/p>\n

\u2018The largest measles epidemic in North America in the last decade, occurred in 2011 in Quebec, Canada, where rates of 1- and 2-dose (MMR) vaccine coverage among children 3 years of age were 95%-97%, with 3%-5% unvaccinated.<\/a>‘ Largest measles epidemic in North America in a decade\u2013Quebec, Canada, 2011: contribution of susceptibility, serendipity, and superspreading events\/PubMed\u00a0\u00a0 <\/strong><\/p>\n

‘The index (initial) case had two doses of measles-containing vaccine. Of 88 contacts, four secondary cases were confirmed that had either two doses of measles-containing vaccine or a past positive measles IgG antibody.<\/a><\/strong><\/p>\n

All cases had laboratory confirmation of measles infection, clinical symptoms consistent with measles, and high avidity IgG antibody characteristic of a secondary immune response. Neutralizing antibody titers of secondary cases reached >80,000 mIU\/mL 3-4 days post-rash onset while that of the index was <500 mIU\/mL 9 days post-rash onset. No additional cases occurred among 231 contacts of secondary cases.<\/a><\/strong><\/p>\n

This is the first report of measles transmission from a twice vaccinated individual. The clinical presentation and laboratory data of the index were typical of measles in a na\u00efve individual…This outbreak underscores the need for thorough epidemiologic and laboratory investigation of suspected measles cases regardless of vaccination status.<\/a>‘ Oxford Journal of Clinical Infectious Diseases, 2011\u00a0 <\/strong><\/p>\n

Note: ‘The index (initial) case had two doses of measles-containing vaccine.<\/a>‘\u00a0 <\/strong><\/p>\n

\u2018<\/strong>An outbreak of measles occurred in a high school with a documented vaccination level of 98 per cent. Nineteen (70 per cent) of the cases were students who had histories of measles vaccination at 12 months of age or older and are therefore considered vaccine failures\u2026Vaccine failures among apparently adequately vaccinated individuals were sources of infection for at least 48 per cent of the cases in the outbreak.<\/strong><\/span><\/a>\u2018 Measles outbreak in a vaccinated school population: epidemiology, chains of transmission and the role of vaccine failures –\u00a0American Journal of Public Health 05\/1987<\/strong><\/p>\n

Note: \u2018Vaccine failures among apparently adequately vaccinated individuals were sources of infection for at least 48 per cent of the cases in the outbreak.\u2019<\/strong><\/p>\n

\u2018<\/strong>Vaccination coverage for the total population was 99.0%. Incomplete vaccination coverage is not a valid explanation for the Quebec City measles outbreak.<\/strong><\/span><\/a>\u2018 Major measles epidemic in the region of Quebec (1989) despite a 99% vaccine coverage \u2013 Boulianne N1, De Serres G, Duval B, Joly JR, Meyer F, D\u00e9ry P, Alary M, Le H\u00e9naff D, Th\u00e9riault N.\/PubMed 1991\u00a0\u00a0\u00a0\u00a0 <\/strong><\/p>\n

‘<\/strong>Numerous outbreaks of disease (Measles) in highly vaccinated populations occur when children in the first few days of illness attend sporting events as participants or spectators, especially indoor events such as basketball and wrestling tournaments. Outbreaks also occur when ill (vaccinated) children are brought to a doctor’s office or emergency room for evaluation for fever, irritability, or rash.<\/strong><\/span><\/a><\/p>\n

Measles has been hypothesized to cause or contribute to multiple sclerosis, but available evidence is weak and inconclusive. Measles or measles vaccines have been suggested to contribute to or induce autism, but available data favor rejection of these hypotheses. Studies from different laboratories have had conflicting evidence for persistence of measles virus nucleocapsid in affected tissue from patients with otosclerosis, Paget’s disease, and inflammatory bowel disease.<\/a>‘ The Journal of Infectious Diseases<\/strong><\/p>\n

Note: ‘<\/strong>95% of the approximately 75 million (US) children under age 18 have gotten two doses of MMR vaccine and there is also a high measles vaccination rate among young adults in their 20\u2019s and mid-30\u2019s because, since 1981, 95% of all children entering kindergarten have received at least one dose of MMR vaccine and three or more doses of diphtheria, tetanus, pertussis and polio containing vaccines.<\/strong><\/span><\/a>‘ National Vaccine Information Center\u00a0\u00a0 <\/strong><\/p>\n

‘The reported coverage of the measles\u2013rubella (MR) or measles\u2013mumps\u2013rubella (MMR) vaccine is greater than 99.0% in Zhejiang province. However, the incidence of measles, mumps, and rubella remains high.<\/a><\/strong><\/p>\n

Measles outbreaks continued in 2008, with 12782 cases reported, which translated to 252.61 per million of the population. From 2009 to 2011, the incidence of measles remained high at 3.14\u201317.2 per million of the population. Similarly, the incidence of mumps increased from 394.32 to 558.26 per million of the population in 2007 and 2008, respectively.<\/a><\/strong><\/p>\n

Finally, the reported cases of rubella increased from 3284 to 4284 in 2007 and 2011, respectively, representing a 30.45% increase or an increase from 65.94 to 78.71 per million of the population.<\/a>‘ Difficulties in Eliminating Measles and Controlling Rubella and Mumps: A Cross-Sectional Study of a First Measles and Rubella Vaccination and a Second Measles, Mumps, and Rubella Vaccination, PLoS One (peer-reviewed open access journal), 02\/20\/2014<\/strong><\/p>\n

‘We describe a case of vaccine-associated measles (Atypical Measles Syndrome) in a two-year-old patient from British Columbia, Canada, in October 2013, who received her first dose of measles-containing vaccine 37 days prior to onset of prodromal (earliest phase of a developing condition) symptoms. Identification of this delayed vaccine-associated case occurred in the context of an outbreak investigation of a measles cluster.<\/a>‘ Eurosurveillance, Volume 18, Issue 49, 05 December 2013\u00a0\u00a0 <\/strong><\/p>\n

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‘In 1985 and 1986, of 152 measles outbreaks in the United States, 101 (66.4 percent) occurred primarily among school-age persons. Many of the\u00a0 school-age measles cases occurred among persons who had previously received measles vaccine.<\/span><\/a>‘\u00a0Public Health Report |v.107(1); Jan-Feb 1992<\/strong><\/div>\n<\/div>\n
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Note: ‘A cohort study conducted at a junior high school showed that, compared with students vaccinated against measles at ages 15 months or older, those vaccinated at ages 12-14 months had a three-fold increased risk of measles.<\/span><\/a>‘<\/strong><\/div>\n
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Vaccine-derived viral shedding lasts anywhere from 2-5 weeks, conservatively, following any (live or attenuated) injection. <\/strong><\/div>\n<\/div>\n<\/div>\n<\/div>\n

‘Overall, measles virus RNA was detected in 10 of 12 children during the 2-week sampling period. In some cases, measles virus RNA was detected as early as 1 day or as late as 14 days after vaccination.<\/a><\/strong><\/p>\n

Measles virus RNA was also detected in the urine samples from all four of the young adults between 1 and 13 days after vaccination.<\/a>‘ Detection of Measles Virus RNA in Urine Specimens from Vaccine Recipients, Journal of Clinical Microbiology, Sept. 1995<\/strong><\/p>\n

Note: ‘<\/strong>Because our research protocol was limited to only 14 days of specimen collection, we were unable to determine the upper limit for the duration of viral RNA in urine.<\/strong><\/a>‘ (They stopped looking for signs of Vaccine-derived viral shedding at 14 days) <\/strong><\/p>\n

Measles, Mumps, Rubella Vaccine (series) \u2013 1st round given at 12-15 months old: \u2018<\/strong>The evidence convincingly supports a causal relationship between MMR vaccine and measles inclusion body encephalitis <\/a>(<\/span>inflammation of the Brain & Meninges\/Meningoencephalitis manifesting as \u2018<\/span>diffuse and\/or focal neuropsychological dysfunction<\/span><\/a><\/strong>‘<\/a> \u2013<\/a> reaction to synergistic heavy metal-excipient accumulation of \u2019sludge\u2019 toxicity) in individuals with demonstrated immune deficiencies.\u2019 P.110 Institute of Medicine Report on Adverse Effects of Vaccines\/2011<\/strong><\/span><\/p>\n

‘Measles inclusion body encephalitis’ is characterized by ‘persistent measles virus infection, causing inflammation in both the white and gray matter and characterized by the presence of nuclear inclusion bodies.<\/a>‘<\/strong><\/p>\n

‘We report a case of measles inclusion-body encephalitis (MIBE) occurring in an apparently healthy 21-month-old boy 8.5 months after measles-mumps-rubella vaccination. He had no prior evidence of immune deficiency and no history of measles exposure or clinical disease. During hospitalization, a primary immunodeficiency characterized by a profoundly depressed CD8 cell count and dysgammaglobulinemia was demonstrated.<\/a>‘<\/strong><\/p>\n

Note: ‘The presence of measles virus in the brain tissue was confirmed by reverse transcription polymerase chain reaction. The nucleotide sequence in the nucleoprotein and fusion gene regions was identical to that of the Moraten and Schwarz vaccine strains; the fusion gene differed from known genotype A wild-type viruses.<\/a>‘ Clinical Infectious Diseases 1999 Oct;29(4):855-61<\/strong><\/p>\n

Official Package Insert: \u2018<\/strong>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\u2019 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<\/strong><\/span><\/a>\u00a0(aborted fetal tissue).’ <\/strong><\/p>\n

The Measles, Mumps, Rubella Vaccine contains 3 live (attenuated or heat-treated\/modified) viruses propagated (grown) in chick embryos. This process alone is cause for alarm, given the CDC’s own internal data, which states that\u00a0‘egg propagation of viruses can lead to genetic changes that might have antigenic implications (mutagenic synergistic changes which can alter the virus, rendering it more virulent).<\/a>‘ <\/strong><\/p>\n

The Rubella component of the MMR vaccine is derived from aborted human fetal tissue: ‘live attenuated rubella virus propagated in WI-38 human diploid lung fibroblasts (aborted fetal tissue)…WI-38 came from lung cells from a female fetus of 3-months (terminated during the 1st Trimester\/United States 1961) gestation.<\/a>‘<\/strong><\/p>\n

The is the primary reason for the massive surge in cases of Autism.<\/strong><\/p>\n

The MMR vaccine factors into the eventuality of Early Onset Autism, since it represents the final blow at 12-15 months, the most intense period in standard immunization, beginning with the Hepatitis B shot at 12 hours old, followed in close succession by the DPT series, IPV, PCV and others; a massive premature breach of a child’s delicate, under-developed \u201celectrical grid system\u201d (Myelin sheath, Meninges & Blood Brain Barrier).<\/strong><\/p>\n

Note: The shot series also contains 25 mcg of Neomycin, a toxic antibiotic, used ostensibly to help prevent bacterial contamination during manufacturing process. Neomycin can cause ‘severe allergic reactions including hives, swelling at the back of the throat, and low blood pressure, and is associated with Kidney failure; also hazardous to a fetus.<\/a>‘<\/strong><\/p>\n

The human diploid cell (aborted fetal cell-line) component, WI-38, came from lung cells from a female fetus of 3-months (terminated during the 1st Trimester\/United States 1961) gestation: <\/strong><\/div>\n
\"mrc5<\/a>\u2018Minced preparations\u00a0were obtained by cutting the tissue in a Petri dish containing GM (growth medium) with paired scalpels or a scissors until the size of each piece approximated l-4 mm3. Fragmented preparations were obtained by tearing apart the tissue with two pairs of forceps in a Petri dish containing GM until the pieces could no longer conveniently be grasped\u00a0 and shredded.<\/a>‘<\/span><\/strong><\/div>\n
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\u2018The WI-38 and MRC-5 cell cultures have been used to prepare hundreds of millions of doses of (following) vaccines \u2013 rubella (third component of the MMR series, administered in 2 doses, first at 12 months old), hepatitis A (administered in 2 doses, first at 12 months old), varicella (chickenpox, administered in 2 doses, first at 12 months old) and rabies (administered selectively pending rabies-related emergency).<\/span><\/a>\u2018 National Network for Immunization Information<\/strong><\/div>\n
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\"human-diploid-cells\"<\/a><\/div>\n
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Human Diploid Cells (aborted fetal tissue) provide the \u201cCell culture\u201d in which vaccine formulas are often grown or nurtured. Current vaccines in circulation which contain aborted fetal tissue include:<\/strong><\/p>\n

1. Polio vaccine (inactivated\/IPV) & Oral Polio (live virus) drops<\/strong>
\n2. Measles, Mumps, Rubella vaccine\/MMR (Rubella component)<\/strong>
\n3. Diphtheria, Tetanus, Pertussis, Poliomyelitis vaccine (DTaP\/TdP)\u00a0<\/strong>
\n4. Varicella (Chickenpox) vaccine & Shingles (zoster) vaccine<\/strong>
\n5. Hepatitis A vaccine<\/strong>
\n6. Rabies vaccine<\/strong><\/p>\n

\u2018Some vaccines\u2014rubella, HepA, RAB-HDC, VAR, ZOS, and one form of IPV (the Poliovax contained in Pentacel)\u2014are grown in cultured human embryo fibroblast cell lines (WI-38 or MRC-5) because these are the only cells that replicate the viruses in high enough titer for mass production (the rubella vaccine strain itself was originally isolated from an aborted fetus with intrauterine infection).<\/span><\/a>\u2018 Monthly Prescribing Reference (MPR) \u2013 Medical Industry Reference Journal<\/strong><\/p>\n

\u2018Today, more than 23 vaccines are contaminated by the use of aborted fetal cells. There is no law that requires that consumers be informed that some vaccines are made using aborted fetal cells and contain residual aborted fetal DNA. While newer vaccines produced using aborted fetal cells do inform consumers, in their package inserts, that the vaccines contain contaminating DNA from the cell used to produce the vaccine, they do not identify the cells as being derived from electively aborted human fetuses.<\/span><\/a>\u2018 Dr. Theresa A. Deisher, Ph.D.<\/span><\/a><\/strong><\/p>\n

\u2018Not only damaged human cells, but also healthy human cells can take up foreign DNA spontaneously. Foreign human DNA taken up by human cells will be transported into nuclei and be integrated into host genome, which will cause phenotype change. Hence, residual human fetal DNA fragments in vaccine can be one of causes of autism spectrum disorder in children through vaccination.<\/span><\/a>\u2018 Spontaneous Integration of Human DNA Fragments into Host \u2013 Dr. Genome K. Koyama, Dr. Theresa. A. Deisher Ph.D. <\/strong><\/div>\n
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Study findings: \u2018<\/strong>In addition to the ingredients listed on the package insert for Meruvax II\u00ae (Rubella virus vaccine live), we detected significant levels of human ssDNA (142 \u00b1 8 ng\/vial) as well as dsDNA (35 \u00b1 10 ng\/vial) fragmented to -215 base pairs in length. The MMR II\u00ae package insert discloses the presence of human fetal residuals nor how much cell substrate dsDNA (double-stranded DNA) or ssDNA (single-stranded DNA) contaminates each dose.<\/span><\/a>\u2018\u00a0 Journal of Public Health\u00a0and Epidemiology, 09\/2014<\/strong><\/p>\n

Note: ng = nanogram (one billionth of a gram)\u00a0 <\/strong><\/p>\n

\u2018The children vaccinated with MMRII, Varicella and Hepatitis A vaccines varied from 19 to 35 months of age at the time of vaccination. Autistic disorder birth year change-points (sudden spike in cases) were identified as 1980.9, 1988.4 and 1996 for the US, 1987 for the UK, 1990.4 for Western Australia, and 1987.5 for Denmark.<\/span><\/a><\/strong><\/p>\n

Change points in these countries corresponded to introduction of or increased doses of human fetal cell line-manufactured vaccines\u2026Further, linear regression revealed that Varicella and Hepatitis A immunization coverage was significantly correlated to autistic disorder cases.\u2019<\/span><\/a><\/strong><\/p>\n

Note: \u2018Autistic disorder change points years are coincident with introduction of vaccines manufactured using human fetal cell lines, containing fetal and retroviral contaminants, into childhood vaccine regimens. Thus, rising autistic disorder prevalence is directly related to vaccines manufactured using human fetal cell lines.<\/span><\/a>\u2018<\/strong><\/p>\n<\/div>\n

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Note: The aforementioned Study verifies that human DNA, the genetic template (blueprint) a child enters the world equipped with, which determines their capacity to thrive, can, in fact, be damaged, lessened, rendered defective AFTER birth, post-vaccination; blowing the entire CDC argument implicating genetics as the primary cause for Autism, completely out of the proverbial water.<\/strong><\/div>\n
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The Measles, Mumps, Rubella (MMR) Vaccine has been praised for decades by proponents of the Vaccine Industry, by Mainstream Media, by the entire western Medical Establishment, for its supposed efficacy & safety, as a means of safeguarding our youngest and most vulnerable from the often debilitating & life-threatening ravages of early childhood viral infections. <\/strong><\/p>\n

“If you repeat a lie often enough, people will believe it, and you will even come to believe it yourself.” Paul Joseph Goebbels, Propaganda Minister in Nazi Germany<\/strong><\/p>\n

On August 27th, 2010, two whistle-blowers came forward with bombshell testimony<\/a>, implicating their employer, Vaccine manufacturing giant, Merck & Co., in a blatant cover-up of the preliminary trial testing behind the current MMR Vaccine.\u00a0\u00a0<\/strong><\/p>\n

Merck Virologists, Stephen A Krahling & Joan Wlochowski, both instrumental in the development of the M-M-R II Vaccine, were instructed by their employers (Merck), to \u201cIdentify a Mumps neutralization assay format that permits measurement of a >95% seroconversion rate (development of antibodies in response to immunization) in the M-M-R\u00ae II (Measles, Mumps, and Rubella Virus Vaccine Live).<\/strong><\/p>\n

\u2018Merck has used improper testing techniques and falsified test data to fabricate a vaccine efficacy rate of 95% or higher.<\/a>\u2019<\/strong><\/p>\n

\u2018Merck added Rabbit antibodies for the singular purpose of altering the outcome of the test by increasing the virus neutralization count (to meet their 95% standard).<\/a>\u2019<\/strong><\/p>\n<\/div>\n<\/div>\n

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\"wi38_HumanLungDiploidFibroblastCell\"<\/a><\/div>\n<\/div>\n

\u2018<\/strong>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.<\/strong><\/span><\/a>\u2019 Journal of Virology, June 2010 vol. 84 no. 12<\/strong><\/p>\n

Note: \u2018simian retrovirus (SRV) was present as genetically defective DNA.<\/a>‘<\/strong><\/p>\n

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 \u2013 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 germ line DNA of babies\/children.<\/strong><\/p>\n

\u2018BKV (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).<\/span><\/a>‘<\/strong><\/p>\n

‘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.<\/span><\/a>‘<\/strong><\/p>\n

Note: This is indicative of the overlapping problems (synergistic toxicity) associated with multiple vaccines in the Standard Immunization regime.<\/strong><\/p>\n

‘The incidence\/prevalence of data indicate the timing of introduction of vaccines & changes in the type & increasing number of vaccines given at one time implicate vaccines as a cause of autism. The MMR II vaccine is contaminated with human DNA from the cell line. This human DNA could be the cause of the spikes in incidence.<\/a>\u2019 Journal of Immunotoxicology, 2011; 8(1): see pages 68\u201379<\/strong><\/p>\n

“<\/strong>At its heart, the GMC (General Medical Council\/UK) hearing has been about the protection of MMR vaccination policy. The case has been driven by an agenda to crush dissent that in my opinion serves the government & pharmaceutical industry \u2013 not the welfare of children.<\/strong><\/span><\/a>” Dr. Andrew Wakefield <\/strong><\/p>\n

\u2018<\/strong>Measles\u00a0vaccine can cause problems (e.g. fatal giant cell pneumonia) in those\u00a0with severely compromised cell-mediated immunity.<\/span><\/strong><\/a>\u00a0If a patient has an impaired cell-mediated immune response, there is\u00a0continued growth of the virus in the lungs leading to giant cell\u00a0pneumonia (such patients may not have a rash). This is rare, but often\u00a0fatal.\u2019 Dr. Margaret Hunt, University of South Carolina School of Medicine<\/strong><\/p>\n

\u2018<\/strong>The\u00a0development of giant cells has been illustrated in tissue cultures\u00a0 infected with adenoviruses and measles viruses, and in ferrets infected\u00a0 with distemper viruses.<\/span><\/strong><\/a>\u2018 Giant Cell Pneumonia: Clinicopathologic and\u00a0 Experimental Studies, J. M. Adams,, D. T. Imagawa,, Miye Yoshimori, R.\u00a0 W. Huntington\u00a0<\/strong><\/p>\n

Note:\u00a0‘Pneumonia is the most common severe complication\u00a0of measles and accounts for most measles-associated deaths.<\/span><\/a>‘<\/strong><\/p>\n

The Physician’s Desk Reference from 2001 has implicated the MMR Vaccine in <\/strong>‘<\/strong><\/span>Severe Afflictions affecting nearly every body system — including blood, lymphatic, digestive, cardiovascular, immune, nervous, respiratory, and sensory disorders.<\/strong><\/span><\/a>‘<\/p>\n

‘Some parents choose not to vaccinate because they had a personal experience that convinced them vaccines are dangerous. Other people have read peer-reviewed studies showing vaccine safety deficits and decided that the risks are greater than the benefits.<\/a><\/strong><\/p>\n

For example, numerous studies have confirmed a link between vaccinations and cancer. Children who are permitted to contract measles naturally are significantly protected against various cancers later in life. In fact, the wild measles virus has oncolytic (anti-cancer) properties. Tumor remissions after measles infection are well documented in the medical literature.<\/a><\/strong><\/p>\n

Children who are required to be vaccinated against measles have had this anti-cancer protection stripped from them for life. They have been forced to trade a reduced risk of contracting measles for an increased risk of developing cancer later in childhood or as an adult.<\/a><\/strong><\/p>\n

I will list just a few of the studies confirming the scientific link between vaccines and cancer:<\/a><\/strong><\/p>\n

Albonico et al found that adults are significantly protected against non-breast cancers — genital, prostate, gastrointestinal, skin, lung, ear-nose-throat, and others — if they contracted measles (odds ratio, OR = 0.45), rubella (OR = 0.38) or chickenpox (OR = 0.62) earlier in life. [Med Hypotheses 1998; 51(4): 315-20].<\/a><\/strong><\/p>\n

Montella et al found that contracting measles in childhood reduces the risk of developing lymphatic cancer in adulthood [Leuk Res 2006; 30(8): 917-22].<\/a><\/strong><\/p>\n

Alexander et al found that infection with measles during childhood is significantly protective — it cuts the risk in half — against developing Hodgkin’s disease (OR = 0.53) [Br J Cancer 2000; 82(5): 1117-21].<\/a><\/strong><\/p>\n

Glaser et al also found that lymph cancer is significantly more likely in adults who were not infected with measles, mumps or rubella in childhood [In J Cancer 2005; 115(4): 599-605].<\/a><\/strong><\/p>\n

Gilham et al found that infants with the least exposure to common infections have the greatest risk of developing childhood leukemia [BMJ 2005; 330: 1294].<\/a><\/strong><\/p>\n

Urayama et al also found that early exposure to infections is protective against leukemia [Int J Cancer 2011; 128(7): 1632-43].<\/a><\/strong><\/p>\n

In the world of science, it is quite well known that having infections in early life protects against various cancers in later life. Later born children have less cancer than first born children because they are exposed to more infections in early life from their siblings. Children that go to daycare in early life are more protected against cancers for the same reason. Vaccinations denied babies opportunities to become naturally infected, and with this reduction in exposure to disease there was a trade-off — increased rates of cancer.<\/a><\/strong><\/p>\n

\u00a0People may legitimately argue over whether the reduction in disease in exchange for an increase in cancer is a good thing or a bad thing but the tradeoff is a real thing that must be considered when weighing the honest risk-to-benefit ratio of vaccinations. Parents are entitled to know this information in order to retain true informed consent, remain free to accept or reject vaccinations and have their human rights preserved.<\/a>‘ Neil Z. Miller, veteran medical research journalist and the author of the Vaccine Safety Manual for Concerned Families and Health Practitioners<\/strong><\/p>\n

\u2018According 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.<\/span><\/a><\/strong><\/p>\n

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.<\/span><\/a><\/strong><\/p>\n

In both The New England Journal and the journal Thorax, articles have appeared stating that a healthy immune system has a \u201cbias\u201d 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.<\/span><\/a>‘ Dr. Harold E. Buttram, MD<\/strong><\/p>\n

Exactly why 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 \u201cimmunized\u201d with the MMR series increases their risk of susceptibility to measles and transference of measles to other children in their proximity.<\/strong><\/p>\n

As Dr Tetyana Obukhanych Ph.D., a prominent Immunologist (guest speaker at our recent VRM Vaccine Summit<\/a>) 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.<\/strong><\/p>\n

Parents who received the first wave of (live) 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\u2019s germ line DNA \u2013 manifesting in a more virulent, persistent strain of measles, known as \u2018Atypical Measles<\/a>\u2018) generated by the shot, passed on to\u00a0each new generation.<\/strong><\/p>\n

‘The vulnerability of very young babies to measles today is the direct outcome of the prolonged mass vaccination campaign of the past, during which their mothers, themselves vaccinated in their childhood, were not able to experience measles naturally at a safe school age and establish the lifelong immunity that would also be transferred to their babies and protect them from measles for the first year of life.<\/a>‘ Immunologist Tetyana Obukhanych, PhD<\/strong><\/p>\n

The current generation have literally become unwitting hosts to a form of viral & bacterial roulette, an ideal breeding ground for the proliferation\/weaponizing of lifelong (inter-generational) viral, bacterial & fungal (gut related) infections.<\/a><\/strong><\/p>\n

\u201cI am very concerned that \u201cimmunologic memory\u201d of adjuvant-containing vaccines is actually the basis of sensitization rather than the basis of immunity. Furthermore, I am very concerned that \u201csuccessful\u201d 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.<\/strong><\/p>\n

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\u2019s immunity. By doing so, vaccination campaigns wipe out population\u2019s 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.<\/strong><\/p>\n

All of this is a direct outcome of the \u201cdesired\u201d vaccination effects, the impact of which hasn\u2019t been carefully thought through in advance of introducing mass vaccination. We thought that vaccines work just like natural immunity. Well, apparently they don\u2019t and we are now reaping the consequences of that.<\/strong><\/p>\n

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.<\/strong><\/p>\n

I think this is happening because vaccination does not engage the genuine mechanism of immunity. Vaccination typically engages the immune response\u2014that is, everything that immunologists would theoretically \u201cwant\u201d 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.\u201d Dr. Tetyana Obukhanych Ph.D<\/a><\/strong><\/p>\n

The overwhelming body of scientific evidence confirms these assertions: Vaccines\u00a0suppress your\u00a0Immunity. In fact, Herd Immunity, itself, is clearly a myth.<\/strong><\/p>\n

‘<\/strong>When infectious diseases of childhood are not mismanaged by the administration of antibiotics, or by suppressing fever, the diseases prime and mature the immune system and also represent developmental milestones. <\/strong><\/span><\/a><\/p>\n

Having measles not only results in l<\/strong><\/span><\/a>ife-long specific immunity to measles, but also in life-long non-specific immunity to degenerative diseases of bone and cartilage, sebaceous skin diseases, immunoreactive diseases and certain tumors.<\/strong><\/span><\/a>‘ Dr. Viera Scheibner (PhD)<\/strong><\/p>\n

\u2018<\/strong>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.<\/span><\/strong><\/a><\/p>\n

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.<\/span><\/strong><\/a>\u2018 Poland GA, Jacobson RM., Department of Internal Medicine, Mayo Vaccine Research Group, Mayo Clinic and Foundation, Rochester, MN.\/1994<\/strong><\/p>\n

\u2018As 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.<\/a><\/strong><\/p>\n

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).<\/a><\/strong><\/p>\n

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.<\/a>‘ Dr Viera Scheibner (PhD), International Medical Counsel on Vaccination<\/strong><\/p>\n

\u2018We 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\u2019s spots. In AMS the rash is morphologically a mixture of maculopapular, petechial, vesicular, and urticarial components.<\/a><\/strong><\/p>\n

It usually begins and is concentrated primarily on the extremities, progresses cephalad, and is not accompanied by Koplik\u2019s 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.<\/a>‘ Dr. E M Nichols M.D.<\/strong><\/p>\n

All those children who receive the MMR Vaccine remain highly susceptible to lifetime viral infections. They retain a more insidious form of the Measles virus than any naturally circulating wild Measles strain found in the environment.<\/strong><\/p>\n

Typically, they will later contract Measles, as teenagers or young adults, often triggered by a vaccinated individual virally shedding person-to-person; albeit a much more virulent strain than that which they would have easily overcome, previously, as a child.<\/strong><\/p>\n

‘The intracellular (Vaccine-derived) measles virus can then survive the acute infection and cause diseases manifesting in the adult age.<\/span><\/a>‘ Department of Epidemiology, State Serum Institute, Copenhagen, Denmark, (Lancet,\u00a001\/05\/1985)\u00a0\u00a0\u00a0\u00a0 <\/strong><\/div>\n
<\/div>\n

\"mmr203\"<\/a>The MMR Vaccine has co-infected an entire generation of children with a more virulent strain of Measles, now referred to as Atypical Measles Syndrome (AMS). <\/strong><\/p>\n

The Medical Industry has reluctantly confirmed this vaccine-derived mutation circulating throughout the environment:<\/strong><\/p>\n

\u2018<\/strong>Atypical measles occurred (occurs) in children who received formalin-inactivated (killed) measles vaccine that was in use in the United States from 1963 to 1968. These children developed high fever, a rash that was most prominent on the extremities and often included petechiae, and a high rate of pneumonitis. Recent studies in monkeys indicate that this illness was caused by antigen-antibody immune complexes resulting from incomplete maturation of the antibody response to the vaccine.<\/strong><\/span><\/a>\u2018 The Journal of Infectious Diseases <\/strong><\/p>\n

\u2018<\/strong>Atypical measles can occur in people who were immunized with a killed virus vaccine that was used from 1963-1967 and then exposed to the original virus. It can also occur in people who were immunized with the current vaccine but, for some reason, failed to develop immunity, and in people who are immunosuppressed.<\/strong><\/span><\/a>‘<\/p>\n

Note: \u2018<\/strong>The symptoms of atypical measles are different and more severe than the symptoms of typical measles<\/strong>.<\/span><\/a>‘<\/p>\n

Symptoms of Vaccine-derived hybrid strain of Measles (Atypical Measles\/AMS):<\/strong><\/p>\n

1. Maculopapular ‘characterised by flat spots (macules) and tiny bumps (papules) on the surface of a tissue\u2014usually understood to mean the skin or an organ (e.g., the liver or spleen).<\/a>\u2019\u00a0\u00a0 <\/strong><\/p>\n

2. Petechial \u2018pertaining to tiny red or purple spots caused by an extravasation of blood into the skin.<\/a>\u2019 <\/strong><\/p>\n

3. Vesicular \u2018composed of or relating to small, saclike bodies.<\/a>\u2019 <\/strong><\/p>\n

4. Urticarial \u2018hives; a vascular reaction of the upper dermis marked by transient appearance of slightly elevated patches (wheals) which are redder or paler than the surrounding skin and often attended by severe itching.<\/a>\u2019<\/strong><\/p>\n

\n
\u2018<\/b><\/span>An 18-month-old boy underwent measles-mumps-rubella (MMR) vaccination under the usual schedule for routine childhood immunization in Italy.<\/b><\/span><\/a><\/div>\n
<\/div>\n
Approximately 8 days later he developed an itchy skin eruption, EM-like, consisting of targetoid lesions with erythematous-oedematous expanding borders, studded with tiny vesicles and pustules on an erythematous base, starting at the trunk and then rapidly involving the whole integument, including the face (with the presence of marked facial oedema).<\/b><\/span><\/a><\/div>\n
<\/div>\n
The patient had received no medications before vaccination or before the onset of his cutaneous eruption. Thereafter, the skin lesions gradually became confluent and polycyclic and within a few days were covered with tiny scales. Excoriations were also observed. There was no evidence of mucosal involvement, fever or respiratory symptoms.<\/b><\/span><\/a>\u2019 Clinic of Dermatology and Pediatrics, Polytechnic University of the Marche, Ancona, Italy, February 1, 2006.<\/b><\/span><\/div>\n
<\/div>\n
Note: \u2018<\/b><\/span>The only relevant data from the medical history was the administration of the MMR vaccination<\/b><\/span><\/a>.’<\/b><\/span><\/div>\n<\/div>\n
\"Atypical<\/a><\/strong><\/div>\n

\u2018<\/strong>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.<\/strong><\/span><\/a>\u2018 Dr. Russell L. Blaylock M.D.<\/strong><\/p>\n

Is it any wonder, that a m<\/strong>utagenic Measles viral strain (atypical measles<\/span><\/a>) commonly infects the bowels\/intestines of children with Autism, manifesting\u00a0as Inflammatory Bowel Disease, ranging from <\/strong>Intermediate\/Advanced Crohns\u00a0to varying degrees of <\/strong>Colitis?<\/strong><\/p>\n

‘In the United States, 8% of all reported measles cases during 1987\u20132000 were complicated by diarrhea. Rates were higher in those <5 or >30 years old. Among hospitalized persons with measles in the United States, 30%\u201370% had diarrhea. Measles-associated diarrhea typically begins just before rash onset, suggesting that measles virus is responsible for most of the diarrhea episodes but that secondary bacterial or viral infections may contribute to the severity and duration of illness.<\/a>‘\u00a0 The Journal of Infectious Diseases<\/strong>\u00a0<\/strong><\/span><\/a><\/p>\n

“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.\u201d <\/strong>Dr. Andrew Wakefield<\/strong><\/a><\/p>\n

‘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.<\/a>\u2019 Dr. Russell L. Blaylock<\/strong><\/p>\n

Government data admits to a probable causal link between vaccines & the (inexplicable) presence of Measles in the bowels of young children<\/a>; while promoting a deliberate cover-up of these inherent risks to the general public,<\/strong><\/p>\n

\u2018That Crohn\u2019s 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.<\/a><\/strong><\/p>\n

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.<\/strong><\/a><\/p>\n

As was stated above, measles vaccine does not seem to be associated with SSPE (subacute sclerosing panencephalitis), although the wild virus may be isolated (with difficulty) in patients with SSPE. The measles virus was isolated neither in patients with Crohn\u2019s disease or other chronic inflammatory diseases (Paget\u2019s disease, active chronic hepatitis, multiple sclerosis) in which a role for it has been claimed on morphologic, histologic or serologic grounds.<\/strong><\/a><\/p>\n

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.<\/a>\u2019 Identification of Genetic Mutations Associated With Attenuation and Changes in Tropism of Urabe Mumps Virus, Journal of Medical Virology 81:130\u2013138\/2009<\/strong><\/p>\n

Note:\u00a0 \u2018\u2026it 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.<\/a>\u2019<\/strong><\/p>\n

Natural Immunity is designed to take on and withstand any incoming infections, either viral, bacterial or fungal pathogens, which threaten your survival. The body can only do this when it is naturally, gradually exposed to disease & infectious agents lurking in the environment.<\/strong><\/p>\n

The science of Vaccines is built on the model of COMBATING or shielding yourself off from the environment, by injecting toxins into deep muscle tissue or subcutaneously; artificially shocking & jump-starting the body into recognizing external \u201cthreats\u201d, rather than holistically EMBRACING all that we come in contact with, thereby re-enforcing, through HARMONY, the inherent properties of natural immunity.\u00a0<\/strong><\/p>\n

All vaccines, by their very nature, play off each other \u2013 a \u201csynergistic\u201d chain-reaction; triggering further infections & disorders. In many cases the very signature disease\/disorder they claim to protect you against is PRECISELY that which they inadvertently spread. \u00a0<\/strong><\/p>\n

Note: The declining health standards in our children is approaching epidemic proportions: ‘It\u2019s estimated that one in 10 Canadian children have severe allergies, asthma, diabetes, epilepsy and other conditions that can be life-threatening if emergencies are not treated properly and promptly.<\/a>‘ Canadian Government<\/strong><\/p>\n

What is the link between Thimerosal, Measles & Vitamin depletion affecting (infecting) our children today?\u00a0<\/strong><\/p>\n

Typically, those living in the West are annually starved of vital UVB Ultra-violet rays (which manifest as the steroid hormone Vitamin D3) throughout the entire duration of Winter & early Spring.<\/strong><\/p>\n

As a result, the Lymphocytes in their lungs cannot process Vitamin C & E, which leads to Respiratory dysfunction & increased vulnerability to ALL infections. Vitamin D is required to increase the circulation of calcium and phosphorous, two minerals necessary for healthy bones.<\/strong><\/p>\n

The kidneys produce Vitamin D3 & the liver plays a vital role in the functioning of D3 throughout the body. Vitamin C is required for the synthesis of collagen, the intercellular \u201ccement\u201d substance which gives structure to muscles, vascular tissues, bones, tendons and ligaments. Vitamin E is an antioxidant which intercepts free radicals and therefore prevents lipid destruction chain reactions. It maintains the integrity of cell membranes. \u00a0 After reactions with free radicals the antioxidant function of Vitamin E is lost. Vitamin C is able to regenerate Vitamin E levels but not when the Vitamin D3 levels drop off. As you can see, when any primary systems are compromised, a chain reaction occurs, throwing off your entire metabolism.<\/strong><\/p>\n

Vaccines & antibiotics drastically deplete the body of these, and other, vital nutrients, notably Vitamin A, which plays a dynamic role in the capacity of your lungs to adapt to viral infections circulating throughout the environment.<\/strong><\/p>\n

‘Administration of vitamin A helps the progression of certain components of the T- lymphocytes (A principal type of white blood cell that completes maturation in the thymus and that has various roles in the immune system, including the identification of specific foreign antigens in the body and the activation and deactivation of other immune cells).<\/a>‘<\/strong><\/p>\n

Thimerosal directly inhibits respiratory function in the body, by neutralizing the interdependent role of Macrophages (white blood cells: key players in the immune response to foreign invaders of the body, such as infectious microorganisms)\u00a0 & Lymphocytes (refined White blood cells: designed to facilitate antibody production) in the lungs; while generating an over-abundance of hyperactive Mast cells<\/a> – a red flag indicator of system-wide immune dysfunction, triggers release of free-radicals<\/a> (unpaired electrons \u2013 highly reactive), further metabolic breakdown (decreased capacity of Mitochondria & Methylation functionality \u2013 viability of cells) and ensuing chronic conditions (Cold, Flu, Strep Throat, Bronchitis, Asthma, Pneumonia).<\/strong><\/p>\n

Note: Mast cells are involved in allergic reactions (Anaphylaxis, a system-wide allergic & functional breakdown, described as \u2018a severe, whole-body allergic reaction to a chemical that has become an allergen<\/a>‘), and also in inflammation (Encephalitis, inflammation of the brain & meninges manifesting as \u2018diffuse and\/or focal neuropsychological dysfunction<\/a>‘), and innate & acquired immunity. <\/strong><\/p>\n

Autistic individuals have a 10-fold greater number of hyperactive mast cells in most tissues.<\/a><\/strong><\/p>\n

Thimerosal Mercury (average 25-75 \u00b5g\/micrograms) is added to all multi-dose vials of Influenza vaccine. There is no safe threshold for Thimerosal exposure in young children.<\/strong><\/p>\n

Thimerosal is now being pushed on pregnant women & babies as young as 6 months old.<\/strong><\/p>\n

‘Mercury is known to be neurotoxic, but its effects on the immune system are less well known. Mast cells are involved in allergic reactions, but also in innate and acquired immunity, as well as in inflammation. Many patients with Autism Spectrum Disorders (ASD) have “allergic” symptoms; moreover, the prevalence of ASD in patients with mastocytosis, characterized by numerous hyperactive mast cells in most tissues, is 10-fold higher than the general population suggesting mast cell involvement…Mercury stimulates vascular endothelial growth factor and interleukin (IL)-6 release from mast cells. These mediators could disrupt the blood\u2013brain barrier and cause brain inflammation.<\/a>\u2019 Kempuraj et al., 2010<\/strong><\/p>\n

Thimerosal literally strips the body of it’s inherent capacity to harness key players in this delicate balance. Without adequate levels of Vitamin A, the lungs become seriously compromised, and cannot fight off incoming viral infections. such as Measles.<\/strong><\/p>\n

Most mainstream doctors refuse to consider these vital aspects of our overall health.<\/strong><\/p>\n

Viral vaccines target\/co-infect the vaccinated recipient with a persistent viral infection that lingers in the organs for years to come, rendering that individual highly susceptible to lifetime viral infections<\/a>, notably Measles, leaving them pre-disposed to Pneumonia.<\/strong><\/p>\n

So are there any practical options? Absolutely. There is a safe, effective solution to overcoming Measles, and adapting to Measles symptoms in the eventuality we do contract the virus. Every child should be taking daily doses of Vitamin A, to boost their capacity for optimal natural immunity (Cod Liver Oil).<\/strong><\/p>\n

According to\u00a0 Dr. Joseph Pizzorno, one of the world’s leading authorities on science-based natural\/integrative medicine,<\/strong><\/p>\n

‘Research shows that now only are children with low Vitamin A levels more likely to get measles, they also get a worse case and suffer an increased rate of side effects and death. Supplementation with even modest amounts of this cheap nutrient results in a very significant improvement in immune function.<\/a>‘<\/strong><\/p>\n

This evidence is reinforced by the Journal of The American Medical Association,<\/strong><\/p>\n

‘Vitamin A supplementation) greatly reduces measles-specific mortality and has been shown to reduce overall mortality in children 6 months and older in the great majority of community studies.<\/a>‘<\/strong><\/p>\n

\u201c<\/strong>For over 100 years, there has been a strong association with vitamin A deficiency and adverse measles outcomes, especially in young children. Has the time come for the medical community to recognize that any child presenting with measles complications should be given vitamin A and evaluated for overall nutritional status? If not, what has history taught us?<\/strong><\/span><\/a>\u201d Adrianne Bendich, 1992<\/strong><\/p>\n

Note: Natural sources of Vitamin A \u2013 Wild Halibut, Cod, Krill & Salmon liver oil, Carrots, Spinach, Celery.<\/strong><\/p>\n

Concentrated doses of Ascorbic Acid (Vitamin C) cleanse all viral pathogens from the body, including strains of Polio, Measles, Chickenpox & Hepatitis.\u00a0\u00a0<\/strong><\/p>\n

‘In poliomyelitis, vitamin C (6,000 to 20,000 mg are administered in a twenty-four hour period intravenously, intramuscularly, and\/or orally – “at least 350 mg per kilogram of body weight.\u201d) performs three important functions:<\/a><\/strong><\/p>\n

1) It destroys the virus; <\/a><\/strong>
\n2) acting as the dehydrator and diuretic of first choice, it removes the edema fluid from the brain and the cord; <\/a><\/strong>
\n3) it preserves the lining of the central canal and maintains more regular spacing and less crowding of the ependymal cells (Altman). The pressure within the bony vault of the central nervous system resulting from the inflammatory process excited by the virus, acts as a haemostat to cut off the blood supply to the anterior horn cells. This compression of their vessels denies to the horn cells the essentials for function, for life even.<\/a>‘<\/strong><\/p>\n

Excerpt from ‘Massive Doses of Vitamin C and the Virus Diseases<\/a>‘ report by F. R. KLENNER, M.D., Reidsville, North Carolina\/April 1951<\/strong><\/p>\n

Note: “With 350 mg per kilogram of body weight every two hours, he could stop measles and dry up chicken pox.<\/a>\u201d Lendon H. Smith\/Clinical Guide to the Use of Vitamin C: The Clinical Experiences of Frederick R. Klenner, M.D<\/strong><\/p>\n

‘Klenner used vitamin C, often accompanied with high doses of other nutrients, to fight a striking variety of other illnesses (including) Rocky Mountain Spotted Fever, bladder infections, alcoholism, arthritis, leukemia, atherosclerosis, ruptured intervertebral discs, high cholesterol, corneal ulcer, diabetes, glaucoma, burns and secondary infections, heat stroke, radiation burns, heavy metal poisoning, chronic fatigue, and complications resulting from surgery. Additionally, Klenner also reported mega nutrient cures of tetanus, trichinosis, venomous bites from spiders or snakes, and, perhaps most controversially, multiple sclerosis.<\/a>‘ Andrew W. Saul, Journal of Orthomolecular Medicine<\/strong><\/p>\n

“Some physicians would stand by and see their patient die rather than use ascorbic acid because in their finite minds it exists only as a vitamin.<\/a>\u201d Frederick. R. Klenner, MD<\/strong><\/p>\n

“When I first came across Klenner\u2019s work on polio patients, I was absolutely amazed and even a bit overwhelmed at what I read. . .To know that polio had been easily cured and so many babies, children, and some adults still continued to die or survive to be permanently crippled by this virus was extremely difficult to accept.<\/a><\/strong><\/p>\n

Many viral infectious diseases have been cured and can continue to be cured by the proper administration of Vitamin C. Yes, the vaccinations for these treatable infectious diseases are completely unnecessary when one has\u00a0 the access to proper treatment with vitamin C.\u00a0And, yes, all the side\u00a0effects of vaccinations are also completely unnecessary since the vaccinations do not have to be given in the first place with the availability of properly dosed vitamin C.<\/a><\/strong><\/p>\n

Amazingly, vitamin C has actually already been documented in the medical literature to have readily and consistently cured both acute polio and acute hepatitis, two viral diseases still considered by modern medicine to be incurable.<\/a>” Dr. Thomas E. Levy, MD, JD<\/strong><\/p>\n

Isn’t it interesting that many of the natural remedies common to our predecessors have since been labelled as “Poisonous” by the gatekeepers of Mainstream Medicine. In the past, for centuries, families utilized Homeopathic (Holistic) remedies, whenever a child succumbed to the current strain of Measles.<\/strong><\/p>\n

Parents would typically administer a blend of plant sources, such as Aconite (Monkshood), White Bryony (also known as Wild Hops), Witch Hazel, Cod Liver Oil (loaded with essential Vitamin A) & Sulphur to their child, to help alleviate the symptoms, and ensure their child a speedy recovery.<\/strong><\/p>\n

Families understood intuitively that by exposing their child to Measles, the body would thus acquire life-long Immuno-protection to Measles in the environment. <\/strong><\/p>\n

Nature is not your adversary. Adaptation is the key. We are not at war with nature.<\/strong><\/p>\n

My point is, Health Authorities are doing a great disservice to families, by not providing this information in a fair and open discussion.<\/strong><\/p>\n

It seems to have been lost on Mainstream Media, but in fact, as early as 70 years ago and previously, Measles parties, like that of Chickenpox parties, were commonplace in most rural communities. Parents purposefully brought their children together, when one had contracted Measles or Chickenpox, such that their own child could be exposed to this wild strain, and thus acquire life-long immune-protection to the virus in the environment. Wisdom of the ages.<\/strong><\/p>\n

Those young parents who oppose vaccinations (ie. the MMR Vaccine) for their family, based primarily on Religious convictions, demonstrate a wisdom beyond their years, trusting in the body’s innate capacity to overcome (adapt to) viral infections, such as Measles, through natural exposure in the environment.<\/strong><\/p>\n

They also recognize that it is fundamentally unscientific, let alone unethical, to inject aborted fetal tissue, laced in the MMR Vaccine, into a child’s bloodstream. ‘Wistar RA 27\/3 strain of live attenuated rubella virus propagated in WI-38 human diploid lung fibroblasts (Aborted Fetal Tissue).<\/a>‘<\/strong><\/p>\n

Whether you profess science or faith as your reasoning behind that ultimate conclusion, the bottom line, those with Religious convictions, who choose to maintain a vaccine-free lifestyle, have seen the light.<\/strong><\/p>\n

Mainstream Media claim the anti-vaccine (pro-holistic health) movement is unscientific. They have vastly under-estimated the intelligence & inherent wisdom of this fast-growing community.<\/strong><\/p>\n

The holistic health movement is SO way ahead of the curve. We recognize that there is clear distinction between the verifiable science of the body, and the detritus of propaganda supporting vaccine theory.<\/strong><\/p>\n

There is no disputing the science of a newborn baby’s brain & central nervous system, the SCIENCE of the electro-chemical synergistic nature of vaccine-derived neurotoxins (Aluminum & Thimerosal) injected into the bloodstream; that, in point of scientific fact, all heavy metals are magnetically drawn to areas of fatty tissue, primarily the brain & central nervous system…where they systematically erode the primary core circuits necessary in supporting early childhood development.<\/strong><\/p>\n

This is where ALL vaccine related neurological damage begins.<\/strong><\/p>\n

Through the annals of history, outbreaks of disease, plague & life-threatening epidemics were primarily the result of over-crowding, marked by insufficient hygiene, sanitation & nutrition. In this day & age, given proper access to clean drinking water, modern sanitation methods & a steady organic diet, there is simply no excuse, here in the West, for the exponential surge in cases of early childhood diseases & disorders now gripping our communities.\u00a0\u00a0<\/strong><\/p>\n

The Vaccine Industry is literally at war with natural immunity, having unleashed a plethora of rogue (hybrid\/rarified) early childhood cancers, virulent \u201cchimera\u201d (weaponized\/mutagenic) viruses, antibiotic resistant bacterium (ie. Methicillin-resistant Staphylococcus aureus\/MRSA) & insidious fungal pathogens (ie. Gut Flora, Candida) upon our youngest & most vulnerable; including a cat\u2019s cradle of neurodevelopmental disorders such as of Autism, ADD, ADHD \u2013 marked by chronic illness & compromised immunity, a rash of auto-immune breakdown related issues (ie. prolonged food\/environmental allergies) & debilitating behavioral difficulties.<\/strong><\/p>\n

The overwhelming body of scientific evidence points to one critical determining factor in the rise of mutagenic viruses & systemic erosion of natural immunity: multi-generational community-wide exposure to the Standard Immunization regime, in particular, those viral vaccines fixed on the schedule which combine multiple live attenuated viruses – ie. the MMR Vaccine.\u00a0\u00a0<\/strong><\/p>\n

Pro-vaccine advocates routinely refuse to acknowledge the mountain of scientific evidence exposing vaccine risk & vaccine-derived injuries, equating these legitimate concerns with “fear-mongering” and “junk-science”. The irony is, they are now increasingly in the minority, and clench on to their mainstream-held indoctrinated beliefs with fear of those in the community who embrace holistic health; while trumpeting their blind trust in an antiquated Vaccine Industry bent on sustaining its own long-term profits.\u00a0 <\/strong><\/p>\n

It seems many of those criticizing self-sufficiency have more concern with praising and preserving the Vaccine Industry, than recognizing & celebrating the merits of the human body itself, the verifiable SCIENCE of holistic health & natural immunity.<\/strong><\/p>\n

The standard use, in the Medical Industry & Mainstream Media, of textbook terminology such as “vaccine-preventable illness or disease” represents a clear contradiction in terms. Vaccines do not, can not, never have & never will prevent illness or disease. Let me repeat that. Vaccines do not, can not, never have & never will prevent illness or disease. Why?<\/strong><\/p>\n

The science of vaccines is imminently flawed. Vaccines no NOT confer immunity. All vaccines straightjacket the immune system, by stripping the body of its ability to harness vital trace minerals & antioxidants; the essential arsenal that any child requires to successfully overcome the symptoms of any incoming infection such as Measles.\u00a0<\/strong><\/p>\n

And they claim we don’t know anything about science.<\/strong><\/p>\n

The Vaccine Industry is literally trying to erase and rewrite the history of our ancestors. <\/strong><\/p>\n

See – Vaccine Resistance Movement interview with CBC National News: <\/strong><\/p>\n

Vaccine Resistance Movement on Vaccine Toxicity & Measles Hype <\/span><\/strong><\/a><\/p>\n

\"Silent<\/a><\/p>\n<\/div>\n

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The Vaccine Resistance Movement is currently launching its first ever educational DVD, the \u2018Silent No More Project<\/a>\u2018: where-in parents of vaccine-injured children reveal intimate details of the impact vaccines had on their child\u2019s primary early development. This ground-breaking event marked the first big push forward following the recent, controversial \u2018VRM Vaccine Summit\u2019.<\/strong><\/p>\n

See: VRM: The Rise of Mutagenic Viruses<\/a><\/strong><\/p>\n

VRM: The Autism Report http:\/\/vaccineresistancemovement.org\/?p=10185<\/a><\/strong><\/p>\n

VRM: Worldwide Autism Study Direct link to study: http:\/\/study.vaccineresistancemovement.org\/<\/a><\/strong><\/p>\n

VRM: The Problem With Vaccines Part 1 http:\/\/vaccineresistancemovement.org\/?p=488<\/a><\/strong><\/p>\n

VRM: Vaccine Clinic \u2013 A Concise Compendium To The Problem With Vaccines<\/strong> http:\/\/vaccineresistancemovement.org\/?p=6278<\/a><\/strong><\/p>\n

VRM: The Problem With Vaccines Part 2 \u2013 Synergistic Effect of Heavy Metal Toxicity On The Body http:\/\/vaccineresistancemovement.org\/?p=6097<\/a><\/strong><\/p>\n

VRM: The Problem With Vaccines Part 3 \u2013 Synthetic Genomics & The Death Of Natural Immunity http:\/\/vaccineresistancemovement.org\/?p=6880<\/a><\/strong><\/p>\n

VRM: A Concise Compendium To The Problem With Vaccines Part 3 \u2013 Synthetic Genomics & The Death Of Natural Immunity http:\/\/vaccineresistancemovement.org\/?p=7283<\/a><\/strong><\/p>\n

VRM: The Problem With Vaccines Part 4 \u2013 Primary Aspects of Vaccine Toxicity Affecting Body http:\/\/vaccineresistancemovement.org\/?p=8787<\/a><\/strong><\/p>\n

VRM: The Problem With Vaccines Part 5A \u2013 Detoxification & Restoration of the Body http:\/\/vaccineresistancemovement.org\/?p=8836<\/a><\/strong><\/p>\n

VRM: The Problem With Vaccines Part 5B \u2013 Detoxification & Restoration of the Body http:\/\/vaccineresistancemovement.org\/?p=8847<\/a><\/strong><\/p>\n

VRM: PCV Vaccine Exposed \u2013 Breeding Ground For Staphylococcus Aureus http:\/\/vaccineresistancemovement.org\/?p=9431<\/a><\/strong><\/p>\n

VRM: Pandemic Preparedness & The Dark Agenda Ahead http:\/\/vaccineresistancemovement.org\/?p=9460<\/a><\/strong><\/p>\n

VRM: Polio \u2013 United Nations & The Great Cull http:\/\/vaccineresistancemovement.org\/?p=4916<\/a><\/strong><\/p>\n

VRM: The Re-emergence of Polio in The Third World (compliments of the World Health Organization & Bill Gates) http:\/\/vaccineresistancemovement.org\/?p=10091<\/a><\/strong><\/p>\n

VRM: Weaponized Polio & The African Green Monkey Conundrum <\/strong> http:\/\/vaccineresistancemovement.org\/?p=10727<\/a><\/strong><\/p>\n

VRM: Mandatory Vaccinatio\u200bns \u2013 How They Will Be Implemente\u200bd http:\/\/vaccineresistancemovement.org\/?p=11806<\/a><\/strong><\/p>\n

VRM: The Confidenti\u200bal Case-files of GlaxoSmith\u200bKline \u2013 Cover-up, Deferral & Denial of Responsibi\u200blity for Vaccine-re\u200blated Premature Deaths http:\/\/vaccineresistancemovement.org\/?p=12242<\/a><\/strong><\/p>\n

VRM: Primary Reasons Not To Get The Flu Shot http:\/\/vaccineresistancemovement.org\/?p=12642<\/a><\/strong><\/p>\n

VRM: The Flu Report http:\/\/vaccineresistancemovement.org\/?p=9226<\/a><\/strong><\/p>\n

VRM: Vaccine Ingredients http:\/\/vaccineresistancemovement.org\/?p=979<\/a><\/strong><\/p>\n

VRM: Safe Alternatives to Vaccines<\/strong> http:\/\/vaccineresistancemovement.org\/?p=662%EF%BB%BF<\/a><\/strong><\/p>\n

VRM: Family Charts Gradual Decline Of Daughter http:\/\/vaccineresistancemovement.org\/?p=3156<\/a><\/strong><\/p>\n

VRM: Health Matters Part 1 http:\/\/vaccineresistancemovement.org\/?p=6719<\/a><\/strong><\/p>\n

VRM: Health Matters Part 2<\/strong> http:\/\/vaccineresistancemovement.org\/?p=6746%EF%BB%BF<\/a><\/strong><\/p>\n

VRM: Alternative Cancer Cures That Work http:\/\/vaccineresistancemovement.org\/?p=3729<\/a><\/strong><\/p>\n

VRM: Pregnancy Tips<\/strong> http:\/\/vaccineresistancemovement.org\/?p=3270<\/a> <\/strong><\/p>\n

VRM: H1N1 Shot Reactions \u2013 Miscarriages http:\/\/vaccineresistancemovement.org\/?p=943<\/a><\/strong><\/p>\n

VRM: The Vanishing Sperm Count http:\/\/vaccineresistancemovement.org\/?p=4639<\/a><\/strong><\/p>\n

VRM: H1N1 Vaccine Surplus From 2009 Reveals Growing Distrust of Gov\u2019t & WHO http:\/\/vaccineresistancemovement.org\/?p=4969<\/a><\/strong><\/p>\n

VRM: Flu Death Statistics \u2013 WHO & The Big Lie http:\/\/vaccineresistancemovement.org\/?p=784<\/a><\/strong><\/p>\n

VRM: Vaccine Industry Deception, Propaganda & Media Collusion<\/strong> http:\/\/vaccineresistancemovement.org\/?p=197<\/a><\/strong><\/p>\n

VRM: Birth of Medical & Scientific Dictatorship \u2013 Future Scenarios http:\/\/vaccineresistancemovement.org\/?p=997<\/a><\/strong><\/p>\n

VRM: H1N1 Bio-weaponry Incorporated http:\/\/vaccineresistancemovement.org\/?p=884<\/a><\/strong><\/p>\n

VRM: Aids & The WHO Connection \u2013 Criminal Intent<\/strong> http:\/\/vaccineresistancemovement.org\/?p=1749<\/a><\/strong><\/p>\n

VRM: Morgellons Syndrome & Chemtrails http:\/\/vaccineresistancemovement.org\/?p=839<\/a><\/strong><\/p>\n

VRM: Council On Foreign Relations 10\/16\/09- Major Influence on Government Vaccine Policy<\/strong> http:\/\/vaccineresistancemovement.org\/?p=1880<\/a><\/strong><\/p>\n

VRM: Closed Door CDC Meeting Reveals Industry Cover-up Of Heavy Metal Toxicity In Vaccines http:\/\/vaccineresistancemovement.org\/?p=5935<\/a><\/strong><\/p>\n

VRM: The Rockefeller Foundation Drafts A Post-Pandemic Scenario http:\/\/vaccineresistancemovement.org\/?p=5102<\/a><\/strong><\/p>\n

VRM: World Health Organization & Vaccine Manufacturers\u00a0Implicated In Massive H1N1 Financial Scam Involving Kickbacks &\u00a0Cover-ups<\/strong> http:\/\/vaccineresistancemovement.org\/?p=4610<\/a><\/strong><\/p>\n

VRM Live \u2013 01\/28\/11: Vaccine Resistance Movement founder Joel\u00a0Lord\u00a0discusses Synthetic Genomics, cloned cell vaccine technology\u00a0& the\u00a0death of natural immunity, gutter journalism & Dr.\u00a0Wakefield\u2019s\u00a0imminent vindication with \u2018Truth to Power\u2019 host Paul Mabelis. http:\/\/www.blogtalkradio.com\/empradio\/2011\/01\/28\/truth-to-power-thursday<\/a><\/strong><\/p>\n

VRM Live <\/strong>– 11\/04\/10<\/strong>: <\/strong>Vaccine\u00a0Resistance Movement founder Joel Lord lays out the whole vaccine\u00a0process\u00a0with Paul Mabelis; including heavy metal toxicity, synergy, pregnancy issues & the basic principles of natural health at risk. http:\/\/www.blogtalkradio.com\/show.aspx?userurl=empradio&year=2010&month=11&day=05&url=truth-to-power-thursday<\/a><\/strong><\/p>\n

VRM Live <\/strong>– 09\/24\/10<\/strong>:\u00a0Vaccine\u00a0Resistance Movement Founder Joel Lord & activist\/radio host Jesse\u00a0Calhoun lay it all out tonite. Topics include the VRM\u00a0Worldwide Autism Study, <\/strong>Scientific\/Medical\u00a0dictatorship, Natural Rights & Vaccine Industry fraud exposed. Special thanks to host Paul Mabelis. http:\/\/www.blogtalkradio.com\/empradio\/2010\/09\/24\/truth-to-power-thursday<\/a><\/strong><\/p>\n

If you appreciate the efforts to bring this information\u00a0forward\u00a0 do consider making a donation. Any amount, no matter how small\u00a0\u00a0 will\u00a0 help enable me to carry on this invaluable research. See Paypal link\u00a0on the VRM website <\/strong>(click on \u2018Donate\u2019 tab in upper right corner)<\/strong><\/strong><\/strong><\/strong><\/strong>. Thank you all.<\/strong><\/p>\n

\"logo.VRM_Ver.2.1\"<\/a><\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"

Do Vaccines actually confer immunity? Is Herd Immunity the stuff of science or myth? This Report explores the link between Vaccines, Herd Immunity & the current resurgence of Measles.\u00a0   The\u00a0World Health Organization (WHO)\u00a0claims vaccination programmes are mutually beneficial to all members within the community. Based on the herd immunity model, vaccines not only\u00a0‘protect the […]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[227],"tags":[],"class_list":["post-13481","post","type-post","status-publish","format-standard","hentry","category-vrm-the-measles-report"],"_links":{"self":[{"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=\/wp\/v2\/posts\/13481","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=13481"}],"version-history":[{"count":141,"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=\/wp\/v2\/posts\/13481\/revisions"}],"predecessor-version":[{"id":15433,"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=\/wp\/v2\/posts\/13481\/revisions\/15433"}],"wp:attachment":[{"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=13481"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=13481"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/vaccineresistancemovement.org\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=13481"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}