BREAKING NEWS: Vaccine Resistance Movement has uncovered scientific proof that the PCV Vaccine, administered at 2, 4, 6 & 12 months of age, is directly responsible for the spread of Methicillin resistant Staphylococcus Aureus (anti-biotic resistant super bug now rampant in most hospitals)
The road-map leading to all neurological & neuro-developmental disorders traces back to the earliest vaccines administered to babies (HEP B, DTaP, PCV, RV, HIB, IPV, MMR). Timing is the key – a premature breach of the delicate, under-developed “electrical grid network” designed to protect the baby’s brain & nervous system (Myelin Sheath, Blood-Brain Barrier, Meninges). It’s not a stroke of genius to utilize basic detective work of this variety.
The proof is in the toxic overload, resulting in all the current manifestations we are witnessing throughout our communities. The WHO, CDC, NIH & all similar Government Health Departments & Institutions around the world, in collusion with major vaccine manufacturers, are implicated in this fraudulent cover-up of the truth. Please wake up, folks! The ENTIRE vaccine Industry is a fraud, period. Vaccine Resistance Movement
Case in point: The PCV Vaccine PREVNAR 13 (Pneumococcal 13-valent Conjugate Vaccine [Diphtheria CRM197 Protein]), part of the standard immunization program throughout the West, is typically administered to babies in 4 stages (2, 4, 6 & 12-15 months) and further given to adults 19-64 with varying chronic conditions (lung, heart, liver or kidney disease; asthma, diabetes, alcoholism/smokers, HIV/AIDS, cancer, damaged/absent spleen). According to the CDC it is ostensibly designed to project against “blood infections, pneumonia, and meningitis, mostly in young children…deafness and brain damage.”
All vaccinated children in the Western hemisphere are now carriers of what is known as MRSA (Methicillin-resistant Staphylococcus aureus/anti-biotic resistant super-bug), due to cross-infection primarily from the routine administering of the Pneumococcal (PCV) Vaccine – in combination with post vaccination anti-biotic & anti-viral drug treatment, an accumulative assault which strips a child of his/her natural anti-biotic resistance whilst infecting them with a host of bacterial serotypes (1, 3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F and 23F); leaving them totally vulnerable to Pneumonia, Myocarditis, Meningitis & even sudden death. The current generation have literally become unwitting hosts to a form of bacterial roulette, an ideal breeding ground for the proliferation & weaponizing of bacterial infections.
This vaccine is also linked to high-grade seizures & chronic infections (ie. ear), again triggered by the series, stemming from the barrage of vaccine derived heavy metals & excipients, resulting in Anaphylaxis, a system-wide allergic & functional breakdown, described as ‘a severe, whole-body allergic reaction to a chemical that has become an allergen‘, and Encephalitis, inflammation of the brain & meninges (Meningoencephalitis) manifesting as ‘diffuse and/or focal neuropsychological dysfunction‘.
‘”I had a baby that was perfectly healthy, happy, okay until she got a shot until she got her vaccine. Thirty, forty hours later, she’s in the hospital having seizures that they can’t stop. You’re not going to tell me it’s not related to the vaccine somehow. It’s hard, it’s very hard. I’m not angry, I’m mad. I guess I’m a little bitter about losing a child. I’m not a little… I’m a lot bitter.” Quote from Ray Graves, father of baby Hayley – who slipped in and out of a coma for 45 days after receiving Prevnar7 (Pneumococcal 7-valent Conjugate Vaccine/Diphtheria CRM197 Protein: Prevnar®), until she died in September, 2001. Tremors shook her little body almost the entire time.
According to Dr. Erdem Cantekin, a medical researcher, one of the leading US experts on earaches, not only are federal regulators issuing bad information, they are also not revealing some of Prevnar’s dangerous side effects. Cantekin says a study by the vaccine’s manufacturer shows seizures happened four times more often in infants given vaccines with Prevnar than children in a control group.
Role of Staphylococcus aureus Catalase in Niche Competition against Streptococcus pneumoniae: ‘Nasal colonization by Staphylococcus aureus is a major predisposing factor for subsequent infection. Recent reports of increased S. aureus colonization among children receiving pneumococcal vaccine implicate Streptococcus pneumoniae as an important competitor for the same niche. Since S. pneumoniae uses H2O2 to kill competing bacteria, we hypothesized that oxidant defense could play a significant role in promoting S. aureus colonization of the nasal mucosa. Using targeted mutagenesis, we showed that S. aureus expression of catalase contributes significantly to the survival of this pathogen in the presence of S. pneumoniae both in vitro and in a murine model of nasal cocolonization.
S. aureus encodes a number antioxidants, including, alkyl hydroperoxide reductase, and staphyloxanthin, which may supplement catalase in defense against H2O2-producing organisms, such as S. pneumoniae.‘ Bonggoo Park, Victor Nizet, and George Y. Liu
Note: ‘Recent reports of increased S. aureus colonization among children receiving pneumococcal vaccine implicate Streptococcus pneumoniae as an important competitor for the same niche.’
‘Bacteria that cause childhood pneumonia and meningitis have evolved to evade vaccines by swapping bits of their genome with other bacteria, according to a new study. Vaccines that protect against these so-called pneumoccoccal infections are designed to recognise a material on the outer surface of a bacterium’s cell called polysaccharide. Each of more than 90 kinds, or “serotypes”, of these bacteria have a different polysaccharide coating.
In 2000, a vaccine that targeted seven serotypes proved highly effective when introduced in the United States. The same formula – which also prevented transmission from children to adults – was adopted in Britain. Over time, however, the vaccine worked less well, so researchers led by Rory Bowden at the University of Oxford set out to discover why. Combining cutting-edge genetic analysis with epidemiology, which examines how disease spreads, they found that the deadly pathogens escaped detection by swapping genes with other, slightly different, bacteria. Remarkably, the exchanged genetic material came from precisely that part of the genome responsible for making the cell’s coating – the area targeted by the vaccine. The bacteria, in other words, had kept their virulence intact but changed their outward appearance.
The researchers identified several such “recombined” serotypes resistant to the vaccine, and one in particular that had spread across the US from east to west over several years. They also observed – for the first time outside a laboratory – that the bugs could swap several parts of their respective genomes at once.
“This is of particular concern, as recombination involving multiple fragments of DNA allows rapid and simultaneous exchange of key regions of the genome within the bug, potentially allowing it to quickly develop antibiotic resistance,” the researchers said.
In both the US and Britain, the original vaccine has been replaced with a new one that targets 13 rather than seven of the telltale serotypes. But the scientists caution that the bacteria will continue to morph into new forms.’ Note: ‘…the bacteria will continue to morph into new forms’.
http://www.scmp.com/portal/site/SCMP/menuitem.2af62ecb329d3d7733492d9253a0a0a0/?vgnextoid=6c533f85a3e25310VgnVCM100000360a0a0aRCRD&ss=asia%20world&s=news
‘Pneumococcal 7-valent Conjugate Vaccine (Diphtheria CRM197 Protein), Prevnar® (manufactured by Pfizer/Wyeth), is a sterile solution of saccharides of the capsular antigens of Streptococcus pneumoniae serotypes 4, 6B, 9V, 14, 18C, 19F, and 23F individually conjugated to diphtheria CRM197 protein. Each serotype is grown in soy peptone broth. The individual polysaccharides are purified through centrifugation, precipitation, ultrafiltration, and column chromatography. The polysaccharides are chemically activated to make saccharides which are directly conjugated to the protein carrier CRM197 to form the glycoconjugate. This is effected by reductive amination. CRM197 is a nontoxic variant of diphtheria toxin isolated from cultures of Corynebacterium diphtheriae strain C7 (β197) grown in a casamino acids and yeast extract-based medium. CRM197 is purified through ultrafiltration, ammonium sulfate precipitation, and ion-exchange chromatography. The individual glycoconjugates are purified by ultrafiltration and column chromatography and are analyzed for saccharide to protein ratios, molecular size, free saccharide & protein.’
http://labeling.pfizer.com/showlabeling.aspx?id=134
‘Prevnar 13 (manufactured by Pfizer/Wyeth) is indicated for active immunization for the prevention of invasive disease caused by Streptococcus pneumoniae serotypes 1, 3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F and 23F. Prevnar 13 is also indicated for the prevention of otitis media caused by Streptococcus pneumoniae serotypes 4, 6B, 9V, 14, 18C, 19F, and 23F. No otitis media efficacy data are available for serotypes 1, 3, 5, 6A, 7F, and 19A. Prevnar 13, Pneumococcal 13-valent Conjugate Vaccine (Diphtheria CRM197 Protein) is a sterile suspension of saccharides of the capsular antigens of Streptococcus pneumoniae serotypes 1, 3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F, and 23F, individually linked to non-toxic diphtheria CRM197 protein. Each serotype is grown in soy peptone broth. The individual polysaccharides are purified through centrifugation, precipitation, ultrafiltration, and column chromatography. The polysaccharides are chemically activated to make saccharides, which are directly conjugated by reductive amination to the protein carrier CRM197, to form the glycoconjugate. CRM197 is a nontoxic variant of diphtheria toxin isolated from cultures of Corynebacterium diphtheriae strain C7 (β197) grown in a casamino acids and yeast extractbased medium. CRM197 is purified through ultrafiltration, ammonium sulfate precipitation, and ion-exchange chromatography. The individual glycoconjugates are purified by ultrafiltration and column chromatography and analyzed for saccharide to protein ratios, molecular size, free saccharide, and free protein.’
http://labeling.pfizer.com/showlabeling.aspx?id=501
The Centers for Disease Control and Prevention (CDC) recommends the vaccine for:
Anyone 65 years of age and older & Adults 19-64 with any of the following conditions:
1. Chronic illnesses such as lung, heart, liver or kidney disease; asthma; diabetes or alcoholism
2. Conditions that weaken the immune system, such as HIV/AIDS, cancer, damaged/absent spleen
3. Cochlear implants or cerebro-spinal fluid (CSF) leaks
4. Adults 19-64 who smoke cigarettes
http://www.adultvaccination.org/doc/pneumo_patient_fact_sheet.pdf
Pneumococcal vaccine. (Minimum age: 6 weeks for pneumococcal conjugate
vaccine [PCV]; 2 years for pneumococcal polysaccharide vaccine [PPSV])
• PCV is recommended for all children aged younger than 5 years. Administer
1 dose of PCV to all healthy children aged 24 through 59 months who are
not completely vaccinated for their age.
• A PCV series begun with 7-valent PCV (PCV7) should be completed with
13-valent PCV (PCV13).
• A single supplemental dose of PCV13 is recommended for all children aged
14 through 59 months who have received an age-appropriate series of PCV7.
• A single supplemental dose of PCV13 is recommended for all children aged
60 through 71 months with underlying medical conditions who have received
an age-appropriate series of PCV7.
• The supplemental dose of PCV13 should be administered at least 8 weeks
after the previous dose of PCV7. See MMWR 2010:59(No. RR-11).
• Administer PPSV at least 8 weeks after last dose of PCV to children aged
2 years or older with certain underlying medical conditions, including a
cochlear implant.
http://www.cdc.gov/vaccines/recs/schedules/downloads/child/0-6yrs-schedule-pr.pdf
‘Children between the 2nd and 6th birthdays with medical conditions such as: – sickle cell disease, – a damaged spleen or no spleen, – cochlear implants, – diabetes, – HIV/AIDS or other diseases that affect the immune system (such as cancer, or liver disease), or -chronic heart or lung disease, or who take medications that affect the immune system, such as immunosuppressive drugs or steroids, should get 1 dose of PCV 13 doses of PCV7 or PCV13 before age 2 years), or 2 doses of PCV13 (if they have received 2 or fewer doses of PCV7 or PCV13). A dose of PCV13 may be administered to children and adolescents 6 through 18 yrs of age who have certain medical conditions, even if they have previously received PCV7/23.’
http://www.cdc.gov/vaccines/pubs/vis/downloads/vis-pcv.pdf
Based on data acquired from the ongoing Vaccine Adverse Events Reporting System (VAERS) Prevnar has been directly linked to ‘28,317 adverse reactions since it was approved in 2000, including 558 deaths, 555 life threatening conditions, 238 permanent disabilities, 2,584 hospitalisations, 101 prolonged hospitalisations, 8,166 emergency room cases and 16,155 “not serious”).
Long-term adverse reactions to PCV Vaccine include the following:
1. An increase in the incidence of pneumonia caused by bacteria NOT covered by these vaccines
2. An increase in middle-ear infections due to bacteria not linked to pneumonia
3. The emergence of “superbugs” (MRSA) that are resistant to vaccines.
http://www.flu-treatments.com/prevnar-vaccine.html
Dutch babies die after PCV vaccine: ‘The PCV vaccine, which is supposed to protect infants and young children against pneumonia, was recently linked to three unexplained infant deaths in the Netherlands. On 5 November 2009, the Dutch government announced that three babies died within two weeks – between one and 11 days – of receiving the vaccine. This is the Prevnar pneumonia conjugate vaccine or PCV, commonly called PCV vaccine, made by drug giant Pfizer.
The response of the Dutch government is hard to comprehend and to accept. Initial press reports sait it banned ONE BATCH of the vaccine but later reports clarified that Pfizer “quarantined” the batch, which contained about 110,000 doses. One would expect that when something as serious as this happens, the health authorities concerned would, at the very least, suspend its vaccination programme pending the results of further investigations. But no. The vaccination programme continued with other batches of the same PCV vaccine. Equally hard to accept is this statement from spokeswoman for the Dutch health institute RIVM: “On average about 5 to 10 deaths are reported annually after babies get vaccines. We now have three cases in a short period; that is unusual, and the reason for suspending the batch.”’
http://www.flu-treatments.com/pcv-vaccine.html
Resistant ‘Superbugs’ Create Need for Novel Antibiotics: New Pneumococcal Conjugate Vaccine – ‘There are now two types of pneumococcal vaccine: pneumococcal polysaccharide vaccine (PneumovaxAE, Pnu-ImmuneAE) and pneumococcal conjugate vaccine (PrevnarAE). Pneumococcal polysaccharide vaccine has been available since 1977 and has been recommended approximately every 5-10 years for older adults and certain at-risk populations. However, this vaccine has not been effective in children under 2 years of age. In February 2000, the FDA approved another form of this vaccine, the pneumococcal conjugate vaccine (PrevnarAE).
In the past, the pneumococcal polysaccharide vaccine was formulated based on certain epidemic serotypes of S. pneumoniae. With the emergence of resistant strains of the organism, a change in the vaccine has been necessary. The pneumococcal conjugate vaccine has been developed which can impart immunity against drug resistant strains of S. pneumoniae. Ex panded use of the newly formulated conjugate pneumococcal vaccine can provide protection against approximately 80% of resistant pneumococcal strains. This form of the vaccine is recommended for children under 2 years of age and other at-risk patient populations. Individuals with risk factors for pneumococcal infection can receive both forms of the vaccine (CDC, 2003).
Superbug resistance is escalating within the clinical setting and community at large. In novative antibiotic strategies are still lacking within the pharmaceutical industry to keep pace with the growing resistance, with a glaring absence of any novel class of antibacterial drug in the United States for decades. Most new antibiotics are chemical modifications of existing drugs and are quickly outsmarted by the bacteria in the environment. Clinicians are challenged by some strains of bacteria which are resistant to essentially all available antimicrobial agents. New antibiotics must be used with precision after the infectious organism is identified by culture and sensitivity testing. Using the exact antibiotic which specifically targets the identified organism is a key strategy to limit bacterial resistance.’
http://www.medscape.com/viewarticle/554935_6
Epidemiology and risk factors for Staphylococcus aureus colonization in children in the post-PCV7 era: ‘In Massachusetts, S. aureus and MRSA colonization remained stable from 2003-04 to 2006-07 among children <7 years despite widespread use of pneumococcal conjugate vaccine. S. aureus nasal colonization varies by age and is inversely correlated with recent antibiotic use.’
http://www.ncbi.nlm.nih.gov/pubmed/19594890
Impact of infant pneumococcal vaccination on invasive pneumococcal diseases in France, 2001-2006: ‘…while the incidence of pneumococcal meningitis and bacteraemia due to non-vaccine strains increased from 9.4 to 17.5 cases per 100,000 in this time period. The incidence in older children and adults did not decrease. Further expansion of PCV coverage is expected to increase the impact of the vaccination in both children and adults. However, the fact that cases caused by vaccine serotypes have been partially substituted by cases of non-vaccine serotypes is likely to reduce the overall benefit of PCV in France, should this early observation be confirmed in the future.
If, on the other hand, the partial substitution of the cases that are caused by vaccine serotypes with cases caused by non-vaccine serotypes, that was observed in our early analysis in young children, is confirmed in the coming years, this would lead to a reduction of the positive impact of PCV vaccination in France.’
http://www.eurosurveillance.org/ViewArticle.aspx?ArticleId=18962
Note: “There’s more risk for MRSA (methicillin-resistant Staphylococcus aureus) to become invasive in the presence of flu or other viruses. These deaths in co-infected children are a warning sign. This is especially alarming given the rising rates of MRSA infections being carried widely among children. It is not common in the U.S. to lose a previously healthy child to pneumonia. Unfortunately, these children had necrotizing pneumonia eating away at their tissue and killing off whole areas of the lung. They looked like immunocompromised patients in the way MRSA went through their body. It’s not that flu alone can’t kill – it can – but in most cases children with flu alone survived…The more antibiotics we take, the more we colonize ourselves with antibiotic-resistant organisms such as MRSA.” Adrienne G. Randolph, MD, Division of Critical Care Medicine at Children’s Hospital Boston
‘During the 2009 H1N1 influenza pandemic, many previously healthy children became critically ill, developing severe pneumonia and respiratory failure, sometimes fatal. The largest nationwide investigation to date of influenza in critically ill children, led by Children’s Hospital Boston, found one key risk factor: Simultaneous infection with methicillin-resistant Staphylococcus aureus (MRSA) increased the risk for flu-related mortality 8-fold among previously healthy children. Moreover, almost all of these co-infected children were rapidly treated with vancomycin, considered to be appropriate treatment for MRSA. The fact that they died despite this treatment is especially alarming given the rising rates of MRSA carriage among children in the community.
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
http://www.childrenshospital.org/newsroom/Site1339/mainpageS1339P791.html
Note: ‘88 percent of the children admitted to the ICU received Tamiflu (oseltamivir) during their stay…’
Eugenics mandate moving full steam ahead: ‘To appreciate how far we’ve come you need to remember where we started. Consider the situation with pneumococcal conjugate vaccines (PCV) in 2003. At that time, developing country access to these vaccines seemed almost unthinkable. The vaccine had only been routinely used in the U.S. for three years, and the manufacturer was struggling to supply American children who paid top dollar prices. Access to affordable supplies of this vaccine was out of the question. In addition, the World Health Organization (WHO) had not yet recommended the vaccine for use and most developing countries had little appreciation for the burden of pneumococcal disease in their countries. Finally, our track record in vaccine access was generally lame, with 15 years or more passing before poor countries accessed the same vaccines as richer ones.
To their credit, GAVI and its Board recognized the importance of pneumococcal vaccines and established GAVI’s PneumoADIP at the Johns Hopkins Bloomberg School of Public Health to accelerate their introduction in the world’s poorest countries. With four years of funding and a small, dedicated team, PneumoADIP aimed to establish, communicate and deliver the value of pneumococcal vaccination by providing the evidence that was needed to make this vaccine a priority.’
http://www.huffingtonpost.com/dr-orin-levine/access-to-the-power-of-va_b_1136823.html
See: VRM: The Flu Report
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BREAKING NEWS: Latest Vaccine Resistance Movement article has uncovered compelling evidence that 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)
‘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
http://www.ncbi.nlm.nih.gov/pubmed/14643124
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 society; with the continued oversight of Western Allopathic Medicine, focusing solely on treating (and thereby exacerbating) Flu symptoms rather than seeking out & remedying (embracing) the underlying cause.
‘Children with preexisting neurologic conditions and immune compromise were at increased risk of pH1N1-associated death after PICU admission. Secondary complications of pH1N1, including myocarditis (inflammation of the heart muscle), encephalitis (inflammation of the brain & meninges), and clinical diagnosis of early presumed MRSA (Methicillin-resistant Staphylococcus Aureus) coinfection of the lung, were mortality risk factors.’ Published in American Academy of Pediatrics, 09/31/11
http://pediatrics.aappublications.org/content/early/2011/11/04/peds.2011-0774.abstract?sid=2f7367a0-a5d8-4ae8-b2f1-b9e16e543085
“There’s more risk for MRSA (methicillin-resistant Staphylococcus aureus) to become invasive in the presence of flu or other viruses. These deaths in co-infected children are a warning sign. This is especially alarming given the rising rates of MRSA infections being carried widely among children. It is not common in the U.S. to lose a previously healthy child to pneumonia. Unfortunately, these children had necrotizing pneumonia eating away at their tissue and killing off whole areas of the lung. They looked like immunocompromised patients in the way MRSA went through their body. It’s not that flu alone can’t kill – it can – but in most cases children with flu alone survived…The more antibiotics we take, the more we colonize ourselves with antibiotic-resistant organisms such as MRSA.” Adrienne G. Randolph, MD, Division of Critical Care Medicine at Children’s Hospital Boston
‘During the 2009 H1N1 influenza pandemic, many previously healthy children became critically ill, developing severe pneumonia and respiratory failure, sometimes fatal. The largest nationwide investigation to date of influenza in critically ill children, led by Children’s Hospital Boston, found one key risk factor: Simultaneous infection with methicillin-resistant Staphylococcus aureus (MRSA) increased the risk for flu-related mortality 8-fold among previously healthy children. Moreover, almost all of these co-infected children were rapidly treated with vancomycin, considered to be appropriate treatment for MRSA. The fact that they died despite this treatment is especially alarming given the rising rates of MRSA carriage among children in the community.
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
http://www.childrenshospital.org/newsroom/Site1339/mainpageS1339P791.html
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.
‘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 viruses1 . 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
http://www.who.int/influenza/patient_care/antivirals/oseltamivir_summary/en/
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).’
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2813201/
‘In 3 studies controlling for disease severity in multivariate analyses, vancomycin resistance was not found to be an “independent” predictor of mortality [17–19]. In another study, when disease severity was not controlled for in the multivariate analysis, vancomycin resistance was an independent predictor of enterococci-associated mortality [5]. In a matched casecohort study [7] that used an alternative approach, 37% mortality was attributed to bacteremia due to vancomycin-resistant enterococci (’Hardy, facultative anaerobic organisms that can survive and grow in many environments…Enterococcus faecalis and Enterococcus faecium are the most prevalent species cultured from humans accounting for more than 90% of clinical isolates.‘).’
http://cid.oxfordjournals.org/content/30/3/466.full.pdf
‘Of the 768 patients colonized with VRE (vancomycin-resistant Enterococcus), 31 (4.0%) usually developed VRE BSI due to a related strain. Independent risk factors for BSI among colonized patients were admission from a long-term care facility, infection of an additional body site, and exposure to vancomycin. Independent risk factors for death were immunosuppression and VRE BSI.’
http://www.ncbi.nlm.nih.gov/pubmed/18419361
Relationship between Vancomycin MIC and Failure among Patients with Methicillin-Resistant Staphylococcus aureus Bacteremia Treated with Vancomycin: ‘The 66 patients with vancomycin MICs of ≥1.5 mg/liter had a 2.4-fold increase in failure compared to patients with MICs (Minimal Inhibitory Concentration – the lowest concentration that is able to inhibit growth of the bacteria) of ≤1.0 mg/liter (36.4% and 15.4%, respectively; P = 0.049). In the Poisson regression, a vancomycin MIC of ≥1.5 mg/liter was independently associated with failure (adjusted risk ratio, 2.6; 95% confidence interval, 1.3 to 5.4; P = 0.01). These data strongly suggest that patients with MRSA bloodstream infections with vancomycin MICs of ≥1.5 mg/liter respond poorly to vancomycin. Alternative anti-MRSA therapies should be considered for these patients.’
http://aac.asm.org/content/52/9/3315.abstract
Body of evidence compiled by VRM includes the following data –
Note: ‘…almost all of these co-infected children were rapidly treated with vancomycin, considered to be appropriate treatment for MRSA (methicillin-resistant Staphylococcus aureus).’
Note: ‘88 percent of the children admitted to the ICU received Tamiflu (oseltamivir) during their stay…’
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.’
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.’
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‘
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).’
Note: ‘Independent risk factors for BSI (blood stream infection) among colonized patients were admission from a long-term care facility, infection of an additional body site, and exposure to vancomycin. Independent risk factors for death were immunosuppression and VRE BSI.’
Note: ‘The 66 patients with vancomycin MICs of ≥1.5 mg/liter had a 2.4-fold increase in failure compared to patients with MICs (Minimal Inhibitory Concentration – the lowest concentration that is able to inhibit growth of the bacteria) of ≤1.0 mg/liter…a vancomycin MIC of ≥1.5 mg/liter was independently associated with failure.’
Note: ‘37% mortality was attributed to bacteremia due to vancomycin-resistant enterococci.’
See: VRM: The Flu Report
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BREAKING NEWS: Britain suddenly replaces the less virulent Cervarix (GSK) with the T-Rex of toxic vaccines currently on the global market, Gardasil (Merck). Guaranteed you can expect a huge surge in cases of otherwise avoidable infertility/sterility, advanced Cervical Cancer, Multiple Sclerosis-like symptoms, Guillaine-Barre Syndrome, Paralysis/Chronic Fatigue Syndrome, Muscle weakness, Dizzyness, Anaphylaxis (severe allergic reaction to toxic ingredients in vaccine involving synergistic response/Blood-Brain barrier breach), Myocarditis (inflammation of the Heart Muscle) & widespread premature deaths throughout the UK
Britain opts for the far deadlier brand of the HPV Vaccine: ‘David Salisbury, the government’s director of immunization, said experts had weighed up both the cost and clinical benefits before deciding to switch to Gardasil. “We have reflected the changes in scientific knowledge that has become available since last time. They are not huge changes — we still prioritize the prevention of cancer — but based on all these things the winner is Gardasil.” Note: “Significant new demand for HPV vaccines could soon open up in the poor nations, following a decision last week by the GAVI international immunizations group to fund their roll-out in developing countries, provided it can reach a deal on pricing with manufacturers.”
http://www.reuters.com/article/2011/11/24/us-merck-sanofi-britain-idUSTRE7AN1TA20111124?feedType=RSS&feedName=healthNews&rpc=22&sp=true
Gardasil ostensibly protects against 4 of the most prevalent genital HPV strains, types 6, 11, 16 & 18; said to account for 70% of cervical cancers & 90% of related genital warts. Given the limitations of Merck’s original clinical trial methods, the fact that malignant cervical cancer takes decades to develop and yet the longest clinical trial on Gardasil was only four years in duration; irrespective of the overwhelming evidence citing a 74% drop in cervical cancer mortality & incidence rates, in developed countries, due to a widespread emphasis on regular pap smears & safe sex and/or abstinence from unprotected sex, the bottom line indicates ‘Gardasil was never shown to prevent cervical cancer.’ Excerpt from VRM: Gardasil/Cervarix – A Legacy Of Shame
The HPV vaccines, Gardasil & Cervarix, contribute to “immune-mediated reactions to the nervous system” resulting in “Motor Neuron Disease” throughout the brain; and for those young teens whose threshold cannot withstand the toxic assault, due to a prolonged, compromised immune system (coupled with pre-existing medical conditions) stemming from the long-term accumulation of vaccine/anti-biotic/bad food choices inflicted erosion/saturation of the brain & gut, the eventuality of “multifocal or atypical demyelinating syndromes” (ie. Multiple Sclerosis). Excerpt from VRM: Gardasil/Cervarix Part 2 – Demyelination, Multiple Sclerosis & the Copaxone Connection
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BREAKING NEWS: VRM editorial comment
As of 2008 cases of Autism Spectrum Disorder were “officially” occurring at a rate of 1 in 67. As of 2009 cases of Autism Spectrum Disorder were “officially” occurring at a rate of 1 in 60. As of 2011 cases of Autism Spectrum Disorder are now “officially” occurring at a rate of 1 in 38 (which translates to 1 in 30 among boys – as they are 4 times more susceptible). Entire divisions of hospitals are devoted to researching the myriad sub-categories & branches of Autism which have metastasized throughout our communities at large.
‘The 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.’ If we don’t do something now, within one generation incidence of cancer & autism will be commonplace in most homes.
Additionally Cancer, once an exceedingly rare occurrence, has literally exploded in numbers. According to the World Health Organization ‘Cancer is a leading cause of death worldwide and accounted for 7.6 million deaths (around 13% of all deaths) in 2008. Deaths from cancer worldwide are projected to continue to rise to over 11 million in 2030.’ We are being domesticated as a society to accept the inevitability of cancer in our daily 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.
There will indeed come a day when vaccination, vivisection, & irradiation will have gone the way of the dinosaur, replaced by non-invasive, genuinely holistic techniques; when Allopathic-type medicine, along with all the ancient tools of its trade, will crumble in the wake of an evolution of consciousness & common sense; when Cancer, Autism, Aids & other encompassing afflictions will have become but a reference footnote in history. Godspeed & good riddance, as they say. May natural immunity be your guiding light through these uncertain times ahead. Words to live by.
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BREAKING NEWS: Recent Study confirms that over 33% of cases of Autism Spectrum Disorder go officially undiagnosed; while overall Autism rates have surged to as high as 1 in 38 (which translates to 1 in 30 among boys – as they are 4 times more susceptible)
‘A study in South Korea suggests about 1 in 38 children have traits of autism, higher than a previous U.S. estimate of 1 in 100. By casting a wider net and looking closely at mainstream children, the researchers expected to find a higher rate of autism characteristics. But they were surprised at how high the rate was. They don’t think South Korea has more children with autism than the United States, but instead that autism often goes undiagnosed in many nations.’
Note: ‘U.S. estimates are based on education and medical records, not the more time-consuming survey conducted in South Korea.’
‘Two-thirds of the children with autism traits in the study were in the mainstream school population, hadn’t been diagnosed before and weren’t getting any special services. Many of those undiagnosed children likely have mild social impairments, rather than more severe autism. “It doesn’t mean all of a sudden there are more new children with [autism spectrum disorders],” said co-author Dr. Young-Shin Kim of the Yale Child Study Center. “They have been there all along, but were not counted in previous prevalence studies.”
http://www.cbc.ca/news/health/story/2011/05/09/autism-prevalence.html?sms_ss=facebook&at_xt=4dc923a541a21846,0
‘Autism spectrum disorders (ASD) in South Korea affect an estimated 2.64% of the population of school-age children, equivalent to 1 in 38 children, according to the first comprehensive study of autism prevalence using a total population sample. The study — conducted by Young-Shin Kim, M.D., of the Yale Child Study Center and her colleagues in the U.S., Korea and Canada — identifies children not yet diagnosed and has the potential to increase autism spectrum disorder prevalence estimates worldwide. Published online today in the American Journal of Psychiatry, the study reports on about 55,000 children ages 7 to 12 years in a South Korean community, including those enrolled in special education services and a disability registry, as well as children enrolled in general education schools. All children were systematically assessed using multiple clinical evaluations. This method unmasked cases that could have gone unnoticed. More than two-thirds of the ASD cases in the study were found in the mainstream school population, unrecognized and untreated.
The research team, including cultural anthropologist Roy Richard Grinker of George Washington University, took steps to mitigate potential cultural biases that could impact diagnostic practices and prevalence estimates. They also considered that more Korean children with ASD may be found in mainstream educational settings based on the design of the highly structured Korean educational system, which often includes 12-hour-long school days. Therefore Korean children with ASD may function at various levels in the Korean general population while not receiving special education services.
“While this study does not suggest that Koreans have more autism than any other population in the world, it does suggest that autism may be more common than previously thought,” said Grinker.
http://news.yale.edu/2011/05/09/prevalence-autism-south-korea-estimated-1-38-children
Timing is CRITICAL. A baby has no blood barrier (physiological mechanism that alters the permeability of brain capillaries so that some substances, such as certain drugs, are prevented from entering brain tissue, while other substances are allowed to enter freely) on the brain – so that vital, unfinished area is still completely raw. The Myelin Sheath, a casing or insulator which protects the baby’s basic cells, is also under-developed. Early Onset Autism, which occurs anywhere from 12-18 months, coincides precisely with most intense period of standard immunization. By 15 months the average child in most developed countries, has received a minimum of 25 injections. This results in severe heavy metal toxicity interfering with the earliest stage of development, during the first 6 months after birth.
A baby’s blood-brain barrier takes no less than 7 months to establish its primary protective shielding: ‘It has been established that by week 28 of the intrauterine development the process of the structural and functional establishment of the BBB (blood-brain barrier) had been over as evidenced by the lack of specific alpha-1-globulin in umbilical blood of the neonates of the given gestation age.’ Volodin NN, Chekhonin VP, Tabolin VA, Rogatkin SO, Kashparov IA.
http://www.ncbi.nlm.nih.gov/pubmed/2471140
The synergy of vaccine derived heavy metal-virus-mycoplasma-excipient toxicity “sludge” targets 3 primary core “electrical grid” stations encasing the nerve center/brain – kin to throwing water over a main keyboard operating system.In the event the blood barrier, Myelin sheath & meninges are breached, particularly at such an early stage in early childhood development, neuro-developmental disorders will inevitably follow. It seems a master Electrician knows more about overall functionality of the human body than your average Pediatrician.
The human body is bio-electric, a huge bio-conductive circuit board that runs throughout the entire body enabling all your systems to function & co-ordinate. You have 60,000 miles of blood vessels coursing throughout the body, a vast array of highways & byways & tributaries that are all inter-connected. The neurons in your brain rely on these ions to generate messages. from your brain throughout the body & back; the regulating of organs, your bloodstream, Heart, Kidney, Liver function – chelating & sequestering, the operation of one’s senses & warning signs, everything related to overall system co-ordination is managed via this delicate bio-conductive process.
Early onset autism occurs anywhere from 12-18 months, potentially even earlier. It is significant that autism coincides precisely with most intense period of standard immunization. According to the CDC’S ‘Recommended Immunization Schedule for Persons Aged 0 Through 6 Years—United States • 2010’ by 15 months the average child has received 25 injections including: 3 doses of Hepatitis B, Rotavirus, HIB (Haemophilus Influenzae Type b), IPV (Inactivated Polio Vaccine) & Hepatitis A, 4 doses of DPT (Diphtheria, Pertussis, Tetanus) & PCV (Pneumococcal Conjugate Vaccine), 1 dose of Varicella & Meningococcal and 2 doses of MMR (Measles, Mumps, Rubella). We hope to clarify not only the immunization time-line factor in relation to the emergence of autism but also the nature of specific vaccines; as to their bearing on each select case of autism reported.
See: VRM: The Problem With Vaccines Part 4 – Primary Aspects of Vaccine Toxicity Affecting The Body
See: VRM Worldwide Autism Study http://study.vaccineresistancemovement.org/
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BREAKING NEWS: The dark eugenics underbelly of Global(ist) Alliance for Vaccines and Immunisations (GAVI) surfacing as country after country faces a widespread looming epidemic of hybrid Polio cases; all the result of a relentless Bill Gates funded multi-billion dollar drive (exceeding $4.3 billion in ‘private-public’ sourced pledges) to vaccinate (contaminate) millions of immune-suppressed children with the Polio virus (triple live virus oral drops) throughout the remote communities of the Third World
‘The government of Pakistan had declared, under its national emergency plan, earlier this year to eradicate polio before 2012. Unfortunately, however, the country seems set to miss this deadline as the number of polio cases in Pakistan soars to 132 so far with two months still to go before the year ends. Adding to the nation’s faltering struggle against this menace, a leaked report prepared by the Prime Minister’s Inspection Commission (PMIC) shockingly reveals that polio vaccines funded by a Swiss NGO are allegedly causing deaths and disabilities in children.
According to the investigative report, the NGO, Global Alliance for Vaccination and Immunisation (GAVI), has been found responsible for funding fatal polio vaccines in not only Pakistan but also India, Sri Lanka, Bhutan and Japan. In Bosnia and Herzegovina, the Association of Parents of Disabled Children has filed criminal charges after they found out that GAVI-funded vaccines cause death or disabilities in children.
This government report reveals information, which should be a source of tremendous concern for the government and parents alike. Far removed from the hope to eradicate polio within this year, the country now hosts more cases of polio than all other three countries, which are still afflicted by this menace – India, Afghanistan and Nigeria – combined. Following China’s confirmation that the disease had crossed Pakistani border into China, resulting in crippling four children, India jumped to pre-emptive safety precautions and announced setting up of screening booths at all entry points along the India-Pakistan border to administer polio drops to children five years or younger.
The draft National Emergency Action Plan, 2011 for polio eradication admitted that 10 to 20 percent of children are not given their third dose of polio vaccination. Added to this, the apocalyptic warnings by some in the clergy and the militants in the north related to “western conspiracies” to sterilise Muslim children through polio drops has also created a sense of paranoia among the traditionally conservative families.
In light of these staggering odds, the fact that a supposedly reputed NGO, which funds 7.8 percent of the five-year budget of Pakistan’s Expanded Programme on Immunisation (EPI), has been the source of potentially fatal and crippling vaccine should ring alarm bells in every corridor of power.
GAVI is supposedly an organisation of repute which boasts partners such as the Bill and Melinda Gates Children’s Vaccine Programme, Rockefeller Foundation, Unicef, WHO and the World Bank. This fact alone is enough to cause doubts over the integrity of other international organisations which associate with GAVI. The Prime Minister needs to take up this report with utmost urgency. He must direct the government to raise its voice at the UN level, and demand explanation why the UN agencies are partnering with an organisation which allegedly endangers the lives of millions of poor children. More importantly, the government needs to hold a proper investigation to find out how the agreement with GAVI was reached before verifying the quality of the vaccines, which according to the report, are also very expensive. The claims made in the report that these vaccines are not even tested in laboratory after procurement to ensure their quality, also need to be re-evaluated.
http://www.brecorder.com/editorials/single/600/0/1252972:deadly-polio-vaccines/?date=2011-11-20
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BREAKING NEWS: World Health Organization finally admits to a correlation between the recent spread of “vaccine-derived poliovirus (cVDPV)” in isolated regions around the world & the UN directed mass vaccination campaign, where-in triple live virus Polio drops are being administered to millions of children throughout these poor communities (estimated 2 billion); part of an ongoing, systemic Private-Public (Gov’t) financed Eugenics drive to sicken & thin out the Third World population
‘The World Health Organization (WHO) is contemplating discontinuing the use of an oral polio vaccine that’s been linked to ongoing outbreaks of the virus in the developing world. WHO is weighing the possibility of using a different formulation of the vaccine, but maintains that patchy implementation of immunization programs, not the vaccine itself, is to blame for the outbreaks.
Since 2000, some two billion children have received more than 10 billion doses of oral polio vaccine containing up to three live strains of the virus, says Oliver Rosenbauer, spokesperson for the WHO’s Global Polio Eradication Initiative. Nineteen outbreaks of circulating vaccine-derived poliovirus (cVDPV) have been documented in that same period, resulting in 536 cases in some 17 countries, the majority in Africa, Rosenbauer says. One outbreak in Nigeria has been ongoing since 2005, with 13 new cases reported so far this year
http://www.cmaj.ca/site/earlyreleases/11nov11_who-mulls-phase-out-of-vaccine-linked-to-polio-outbreaks.xhtml
BREAKING NEWS: Sudan should definitely expect a riptide of new cases of vaccine-derived hybrid Polio strains rippling throughout its many local communities, as the UN-directed Eugenics mandate rolls out, rapidly infecting over 3 million children with three strains of live Polio virus via the oral drops transmission. These children will now become carriers, viral shedding for weeks to others with compromised immune systems, including family, friends, neighbors. All will become vulnerable and many unfortunates will succumb. Thank you, oh great exalted United Nations! Job Well done. You have become enemy number one of natural health freedom & an anathema to natural immunity throughout the world
‘Up to 3.2 million South Sudanese children have received vaccinations against polio in a United Nations-backed campaign to ensure the new country remains free of the deadly disease, more than two years after the last case was reported. Over 20,000 people fanned out across the country’s 10 states over five days last week to reach all children under the age of five in the second round of a three-phase campaign that will conclude with further vaccinations next month.
The campaign, coordinated by South Sudan’s health ministry, is being backed by the UN Children’s Fund (UNICEF) and the UN World Health Organization (WHO). UNICEF bought the vaccines and WHO is assisting with monitoring and surveillance during the campaign. Each child received two drops of the polio vaccine and was then marked by ink on the small finger of the right hand to indicate they had been immunized. Vaccinators went from house to house and village to village to reach targeted children.’
http://www.scoop.co.nz/stories/WO1111/S00445/millions-of-south-sudanese-children-receive-polio-vaccine.htm
According to the World Health Organization vaccines aren’t to blame for the spread of Polio in Nigeria; but rather low vaccine uptake amongst the poorest communities. This despite the fact that, by their own admission, children receiving LIVE POLIO VIRUS DROPS will continue shedding the virus amongst their family & neighbors for weeks to come.
“At the main hospital in Mbarara during that month of 1977 more than 600 children died following polio vaccination.” United Nations
The madness of “herd immunity”, the assumption that by vaccinating (infecting) everyone the herd will somehow maintain overall protection against life threatening diseases & viruses. This inverted logic serves only one agenda, that of a sustained Eugenics directive throughout the Third World. Since the introduction of this program Polio numbers have exploded in these isolated communities. The locals know full well it is Malaria (coupled with crippling poverty, a lack of proper sanitation & nutrition), NOT Polio which presents a genuine threat to their communities.
The only solution – a radical upgrade of sanitation, hygiene & nutritional standards throughout these communities; not more mass vaccinations programs which spread otherwise dormant diseases to poor remote regions. You’ll never see the UN funding that type of a project in any Third World Nation. It would actually save lives & put them on a road to real long-term independence. Eugenics is always couched in “humanitarian” forms of deception.
“In Africa polio does not kill anybody and they say it’s very rare to catch. It’s really very rare to get paralytic polio. They say it’s in very rare circumstances, so what is it that is killing people in Africa? Malaria. Every five seconds a child is dying of malaria in Africa. Now to get the dose of life-saving anti-malaria is about $5 but there is no government to give anti-malaria. When somebody gets malaria, if they have no money they even die. So the question I was asking and many people were asking was ‘If you really want to help children, why begin with a disease that they don’t have?”
SALK/SABIN POLIO VACCINE SPAWNED A HOST OF NEW CANCERS & SYNDROMES INCLUDING:
Mesothelioma (fatal tumor of the membrane surrounding the lungs), Brain cancers (Primarily Ependymomas & Choroid Plexus Tumors, but also Astrocytomas, Glioblastomas, Medulloblastoma, Meningiomas), Bone cancers (Primarily Osteosarcomas, but also Chondrosarcoma & Giant Cell Tumors), Post-Polio Syndrome, Chronic Fatigue Syndrome, Myalgic Encephalomyelitis, Aseptic Meningitis & Non-Hodgkin Lymphoma
See: VRM: Polio – United Nations & The Great Cull
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BREAKING NEWS: Major new study confirms the efficacy of using readily available over-the-counter liquid form Vitamin D3 over that of the frequently administered Doctor recommended prescription Vitamin D2
‘Fifty randomised trials with 94,148 participants provided data for the mortality analyses. Most trials included elderly women (older than 70 years). Vitamin D was administered for a median of two years. More than one half of the trials had a low risk of bias. Overall, vitamin D decreased mortality (RR 0.97, 95% confidence interval (CI) 0.94 to 1.00, I(2) = 0%). When the different forms of vitamin D were assessed separately, only vitamin D(3) decreased mortality significantly (RR 0.94, 95% CI 0.91 to 0.98, I(2) = 0%; 74,789 participants, 32 trials) whereas vitamin D(2), alfacalcidol, or calcitriol did not.
Vitamin D in the form of vitamin D(3) seems to decrease mortality in predominantly elderly women who are mainly in institutions and dependent care. Vitamin D(2), alfacalcidol, and calcitriol had no statistically significant effect on mortality. Vitamin D(3) combined with calcium significantly increased nephrolithiasis (Kidney Stones). Both alfacalcidol and calcitriol significantly increased hypercalcaemia (condition in which the calcium level in your blood is above normal, resulting from an overactivity in one or more of your parathyroid glands, which regulate blood calcium levels).’ Department of Internal Medicine – Gastroenterology and Hepatology, Medical Faculty, University of Nis, Zorana Djindjica 81, Nis, Serbia
http://www.ncbi.nlm.nih.gov/pubmed/21735411
Note: There is a risk of acquiring Kidney Stones in the Ureter/Bladder when Vitamin D3 is used regularly in combination with Calcium (notably from Milk-derived Casein). The solution? Eliminate all pasteurized, homogenized & skim milk products from your diet. Switch to Kefir and make sure to eat plenty of organic Celery instead. Highly recommended.
We must look to children with Autism to determine the full extent of “vaccine toxicity” derived nutrient deficiencies incurred in the body. All vaccine damaged babies or infants, those fortunate enough to miss the onslaught of Early Onset Autism, still incur significant damage to these interdependent storehouses of vitamins/antioxidants & trace minerals (coupled with the body’s inability to break them down accordingly); the end result of which a cascading breakdown ensues at the cellular level – Mitochondrial & Methylation-related dysfunction, including a breach of “electrical grid” nerve center.
It is critical to begin replenishing the body of these vital vitamins/antioxidants (Vitamin’s A, B6/B12, C, D3, E, Glutathione) & trace minerals (Selenium, Magnesium) immediately. Ideally you want to seek out complementary, natural organic sources rich in these select elements. The body can better assimilate their properties (holistically) when these foods are consumed in their raw, uncooked form. Juicing is always optional, however there is always the potential for a system overload (which can hinder Thyroid function – the unleashing of an over-abundance of free radicals in the body); where-as the proportional levels are never exceeded in the raw, natural (organic) food format.
Natural organic fruit/vegetable/plant/oil//fish/meat “sea & soil based” sources rich in vitamins/antioxidants/minerals include:
Sources of Vitamin A – Wild Halibut, Cod, Krill & Salmon liver oil, Carrots, Spinach, Celery
Sources of Vitamin B6 – Wild Snapper & Salmon flesh, organic Bell Peppers, Spinach, Baked Potatoes, Green Peas, Celery, Yams, Broccoli, Asparagus, Turnip Greens, Lentils, Chickpeas, Kidney Beans, Wheat Germ, Sunflower Seeds, Cashews & Hazelnuts
Sources of Vitamin B12 – Sardines, Beef & Kidney Liver, Free-range Eggs
Sources of Vitamin C – Organic Goose/Straw/Blue/Black/Rasp/Goji/Noni/Elderberries, Guava, Lime, Orange, Cantaloupe, Tomato, Celery, Cabbage, Cauliflower, Amaranth, Potato, Radish
Sources of Vitamin D3 – Regular, measured exposure to natural ultra-violet sunlight, Coconut Oil (internal & external), Aloe Vera gel (external), Wild Halibut, Cod, Krill, Shark & Salmon Liver Oil (internal), light exposed Mushrooms (internal), Goose/Straw/Blue/Black/Rasp/Goji/Noni/Elderberries (internal)
Sources of Vitamin E – Organic Wheatgerm/Safflower/Sunflower/Olive oil, Spinach, Broccoli, Hazel/Pine/Peanuts, Almonds, Sardines, Herring
Sources of Glutathione – Curcumin/Tumeric spice, Asparagus, Milk Thistle, Undenatured/non-heat treated Whey Protein “We literally cannot survive without this antioxidant.” Earl Mindell, R.Ph., Ph.D.
Sources of Selenium – Brazil nuts (dried, unblanched), Sesame Seeds, Mollusks, Oyster, Lobster, Shrimp, Herring, Liver, Egg, Beef, Oats, Brown Rice, Garlic, Broccoli, Wheat Germ, Whole Grains, Mushrooms, Red Grapes
Sources of Magnesium – Pumpkin & Squash Seed kernels, Brazil Nuts, Almonds, Cashews, Peanuts, Buckwheat, Black/White Soy Beans, Brown Rice, Halibut, Probiotic Yogurt/Kefir, Celery
Note 1: Blueberries (flavonoids) help to stave off Parkinson’s disease (classic neuro-degenerative type disorder associated with vaccine derived synergistic heavy metal “sludge” toxicity breaching of the Blood-Brain area & demylenation/scarring of Myelin Sheath). “Our findings (Harvard School of Public Health) suggest that flavonoids, specifically a group called anthocyanins, may have neuroprotective effects. If confirmed, flavonoids may be a natural and healthy way to reduce your risk of developing Parkinson’s disease.“…’Flavonoids, namely curcumin, quercetin, ferulic acid and ellagic acid, particularly in a mixture, have been found to block the ability of the (vaccine) adjuvants to trigger a long-term immune reaction. If you take it an hour before the vaccination, it should help dampen the immune reactions.‘
Black rice is loaded with antioxidants, rivaling even blueberries – ‘Anthocyanin antioxidants have shown promise in fighting heart disease, cancer and other diseases. Several studies have shown they can reduce blood levels of low-density lipoprotein cholesterol, also known as LDL or bad cholesterol….”Just a spoonful of black rice bran contains more health-promoting anthocyanin antioxidants than are found in a spoonful of blueberries, but with less sugar and more fibre and vitamin E antioxidants.”‘
See: VRM: The Problem With Vaccines Part 5B – Detoxification & Restoration of the Body
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BREAKING NEWS: VRM editorial comment
The ENTIRE Vaccine Industry is a fraud, period. Shout it loud, shout it proud. I invite you to question your beliefs, challenge the status quo, and in doing so reclaim the essence of self-determination of the body. Your Government has been lying to you for generations. They have no intention of enabling you to discover your ultimate capacity for self sufficiency. That is why you must find your way out of the labyrinth they have spun for you, and turn your back on western Allopathic Medicine forever.
We were never meant to die so young, endure the struggle of myriad hybrid cancers, chronic infections, debilitating diseases, the overwhelming rate of Autism throughout our community (now 1 in 50 in girls, 1 in 38 in boys), & widespread prolonged compromised immunity. We have been lied to. It is time to admit it and take charge once and for all. VRM
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BREAKING NEWS: Our children are systematically being turned into anti-psychotic drug junkies, in many instances with their parents’ consent. The legacy of prescription drug abuse forced on our youngest & most vulnerable, carries with it many dire, long-term consequences including chronic Diabetes, Thyroid impairment, hypertension & high blood pressure linked to Cardiovascular disease, Sterility/Infertility, Cognitive disfunction and prolonged obesity. This destructive pattern has to stop
‘Second-generation anti-psychotics (SGA) are increasingly used to treat children and adolescents…no clinically significant superiority in efficacy has been demonstrated for any specific anti-psychotic, including both first- and second generation agents, in children and adolescents. Major differences exist, however, with respect to type and severity of adverse effects; therefore the choice of treatment is primarily guided by tolerability and safety considerations. Children appear to be at higher risk than adults for a number of adverse effects, such as extrapyramidal symptoms and metabolic and endocrine abnormalities.
Pharmacoepidemiological studies using databases from both the U.S.A and several European countries have documented that the use, although showing wide variability in absolute terms across countries (Zito et al., 2008), has at least doubled during the last ten years (Cooper et al., 2004, Olfson et al., 2006; Aparasu and Bhatara, 2007; Kalverdijk et al., 2008; Rani et al., 2008).
In parallel, it has become apparent that psychiatric disorders often have their onset in childhood, so that conditions such as depression, bipolar disorder, anxiety disorders, and obsessive–compulsive disorders, which were the almost exclusive domain of adult psychiatry, have been increasingly diagnosed and treated also in children and adolescents (Paus et al., 2008).
The data in children and adolescents are overall consistent with those in adults, where a wide heterogeneity in tolerability profile within both first- and second-generation anti-psychotics has been documented, with no evidence of specific efficacy of SGA on negative symptoms (Leucht et al., 2008). Moreover, also the SGA can, with a varying degrees, cause extrapyramidal adverse effects (Correll, 2008b), and metabolic adverse effects can emerge during treatment also with first-generation antipsychotics (Correll and Carlson, 2006; Correll, 2008a), thus blurring the separation between these two categories of anti-psychotics.
There are indications that children are more sensitive than adults to the metabolic adverse effects of SGA, as well as to the extrapyramidal effects of the first-generation anti-psychotics (Correll et al., 2006). Children tend to gain proportionately more weight and do so more rapidly during treatment than adults (Correll and Carlson, 2006). In a recent randomized trial comparing olanzapine versus quetiapine, in adolescent patients with a first psychotic episode, the increment in weight was 15.5 kg and 5.5 kg over 6 months respectively. These increments are rarely seen in adults
(Arango et al., 2009). Consistently across studies and like in adults, olanzapine seems to be especially prone to inducing metabolic adverse effects and related adverse health outcomes (Sikich et al., 2008; Fraguas et al., 2008; Castro-Fornieles et al., 2008). Based on currently available data, it appears that olanzapine cannot be considered a first-line anti-psychotic medication for the treatment of children and adolescents.
Because drug-induced metabolic changes can persist over time and may not be fully reversible upon drug discontinuation, the implications for distal health outcomes can be profound. Age-inappropriate weight gain and obesity increase the risk for a variety of negative outcomes, such as diabetes, hyperlipidemia, and hypertension, which are major risk factors for cardiovascular diseases and reduced quality of life and life expectancy (Correll and Carlson, 2006).
As treatment is administered at a time of rapid brain development, there is a need to evaluate the possible impact, either favorable or detrimental, of anti-psychotic medications on cognition and other aspects of brain maturation at various ages and duration of exposure. Only very limited data are currently available about cognitive functioning during anti-psychotic treatment in children (Aman et al., 2008). In addition to helping identify the effects of medications on physical, mental, and sexual development, it will also be necessary to determine if such effects are either partially or fully reversible, and under which circumstances. In this context, more animal studies are also needed to assess the effects of anti-psychotic exposure on neurotransmitter systems development (Moran-Gates et al., 2006).’ Elsevier Review
http://psicofarmacologia.info/curso/Vitiello.pdf
‘Once reserved for schizophrenia and mania in adults, one antipsychotic alone, risperidone, was recommended by Canadian office-based doctors for children 17 years old and younger 340,670 times in 2010 — a near-doubling since 2006 — according to data provided to Postmedia News from prescription-drug tracking firm IMS Brogan. Another antipsychotic — quetiapine — was recommended to Canadian children 160,700 times.
The increase in prescriptions for children as young as six is raising concerns the drugs are being overused. Some experts say too little is known about the effects on a child’s cognitive, social and physical development.
In 2005-09, anti-psychotic drug recommendations for children and youth in Canada increased 114%, says an article in this month’s issue of the journal Paediatrics & Child Health. The drugs — which have not been approved in Canada for children under 18 — are being used for attention-deficit/hyperactivity disorder, conduct disorders, irritability related to autism, mood disorders, physical or verbal aggression and other behavioural problems.’
http://news.nationalpost.com/2011/11/09/antipsychotic-drugs-for-children-may-be-overused/
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BREAKING NEWS: US Centers for Disease Control (CDC) caught in hot water again as Senior Health Scientist & Human Resources Specialist have been arraigned on charges of corrupting a minor & bestiality
Dr. Kim Lindsey, Deputy Director “second in command” for the Laboratory Science Policy & Practice Program Office at the Centers for Disease Control and Prevention (CDC) & former Senior Health Scientist in the Office of Public Health Preparedness & Response ‘has been arrested over allegations of bestiality and child molestation. DeKalb County police allegedly found photographs of Lindsey performing sex acts on two of her pets.
The Huffington Post notes that Lindsey’s live-in boyfriend, Thomas Westerman, was also charged with two counts of child molestation, but he was not charged with bestiality. The child molestation took place between January 2010 and August 2010. Lindsey and her boyfriend allegedly used the child during sex.
“The bestiality charge is a result of evidence recovered during the investigation. The investigation is still is active and we are not releasing further details.”’
http://www.inquisitr.com/149615/cdc-official-kimberly-lindsey-charged-with-bestiality-child-molestation/
‘In her 12 years at the CDC, Lindsey has received 12 awards for outstanding performance on projects and programs, according to her bio on Emory University’s Biological and Biomedical Sciences website. Lindsey earned her doctorate in immunology and molecular pathogenesis from the university in 1998, a year before she began work at the CDC…A LinkedIn Web page for a Thomas Westerman lists him as having been a watch officer at the CDC from November 2009 to November 2010 and a resource management specialist since August 2011…CDC spokesman Tom Skinner said the agency is aware of the case but cannot comment on personnel issues.’
http://www.cnn.com/2011/10/11/justice/georiga-cdc-arrest/index.html
‘Dr. Lindsey played an important role in the 2009 H1N1 swine flu pandemic campaign, which ended in tragedy for countless many—not from a killer flu (statistically, the 2009 H1N1 flu was MILDER than usual) but from the dangerous and expensive “remedy” to this oversold non-threat.’
http://articles.mercola.com/sites/articles/archive/2011/10/28/cdc-director-arrested-for-child-molestation–bestiality.aspx?e_cid=20111028_DNL_art_1
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BREAKING NEWS: Blatantly misleading Vaccine Industry propaganda now encourages pregnant women to get Influenza vaccine; endangering fetus while putting newborns at serious risk of immediate/long-term harm
‘Getting a seasonal flu vaccination while pregnant protects newborns from the flu for months after birth and won’t cause a miscarriage. So say studies scheduled to be presented Thursday at the annual meeting of the Infectious Diseases Society of America (IDSA), in Boston. “Pregnant women are understandably concerned about protecting their unborn babies, which makes it all the more important for them to understand that getting a flu shot during pregnancy is an important way to protect the baby, as well as themselves. These new data on the safety and effectiveness of these vaccines is reassuring, and the increasing number of pregnant women receiving the vaccine affirms that women are hearing the message about the vaccine’s benefits,” Dr. Kathleen Neuzil, a member of IDSA’s Pandemic Influenza Task Force and a clinical professor in the School of Medicine at the University of Washington, Seattle, said in a society news release.’
http://www.cbsatlanta.com/story/15739319/flu-shots-for-pregnant-women-also-protect-newborns
It should come as no surprise that many pregnant women reported miscarriages during 2009’s H1N1 vaccination campaign. Of those who received the shot upwards of 3,600 cases of miscarriages and stillbirths have been reported, based on current estimates. Bare in mind that figure represents only approximately 10% of the overall numbers. Meaning only 10% of cases are ever reported officially. That translates to upwards of 30,000 possible vaccine induced miscarriages having actually occurred in the US alone.
‘A shocking report from the National Coalition of Organized Women (NCOW) presented data from two different sources demonstrating that the 2009/10 H1N1 vaccines contributed to an estimated 1,588 miscarriages and stillbirths – as high as 3,587 cases. Studies conducted by the CDC have been shown to miss from 10% to 90% of the actual cases because of under-reporting.’
http://www.progressiveconvergence.com/Final%20Press%20Release%20CDC%20Allegedly%20falsified.pdf
The mother’s placenta, & breast milk (Colostrum) are inextricably linked, providing a baby’s primary initial source of nourishment through the long journey of formation in utero; while supplying the basic building blocks of life necessary to guarantee a safe transition into early childhood development. It seems almost inconceivable given the scientific literature in circulation, but somehow the CDC, WHO & local health authorities in countries around the world have begun vehemently recommending all pregnant women & babies as young as 6 months receive the seasonal flu vaccine during first trimester. It is common knowledge in medical circles that Thimerosal crosses not only the blood barrier into the brain, but also gets absorbed into the placenta when introduced to the bloodstream. Their justification borders on attempted infanticide.
‘Flu shots are a safe way to protect the mother and her unborn child from serious illness and complications of flu. The flu shot has been given to millions of pregnant women over many years. Flu shots have not been shown to cause harm to pregnant women or their babies. It is very important for pregnant women to get the flu shot. Having a fever caused by flu infection or other infections early in pregnancy can lead to birth defects in an unborn child. Pregnant women who get a fever should treat their fever with Tylenol® (or store brand equivalent) and contact their doctor as soon as possible.’ CDC
http://www.cdc.gov/flu/protect/vaccine/pregnant.htm
NOTICE TO ALL MOTHERS-TO-BE: YOU SHARE THE SAME IMMUNITY WITH YOUR BABY DURING ALL 3 TRIMESTERS OF YOUR PREGNANCY AND FOR THE ENTIRE PHASE IN WHICH YOU INTEND TO BREAST-FEED YOUR BABY AFTER THEIR BIRTH. ANY VACCINES OR DRUGS RECEIVED BY THE MOTHER DURING THIS DELICATE PERIOD WILL DIRECTLY INHIBIT THE EARLY DEVELOPMENT OF YOUR FETUS/BABY. PLEASE THINK TWICE BEFORE MAKING ANY SUCH DRASTIC DECISION.
IN POINT OF FACT WHAT YOUR BABY DOES NEED IS FOR YOU TO ENSURE YOUR OWN NATURAL IMMUNITY IS THRIVING, THAT YOUR VITAL TRACE MINERAL COUNT, PROTEIN LEVELS, THYROID FUNCTIONALITY, 72% ALKALINITY & BODILY SUPPLY OF PRIMARY ANTI-OXIDANTS/VITAMINS IS AT AN OPTIMAL LEVEL THROUGHOUT THIS CRUCIAL WINDOW OF TIME.
See: VRM: Pregnancy Tips
See: VRM: The Problem With Vaccines Part 4 – Primary Aspects of Vaccine Toxicity Affecting The Body
See: VRM: “One For All” Universal Flu Vaccine – 21st Century Genetic Roulette Part 1
See: VRM: Medical Industry Studies Prove Influenza Vaccine Is Both Dangerous & Ineffective
See: VRM: The Problem With Vaccines Part 5A – Detoxification & Restoration of the Body
See: VRM: The Problem With Vaccines Part 5B – Detoxification & Restoration of the Body
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BREAKING NEWS: Western Society is fast becoming a Prescription drug-addicted cesspool of zombies – compliments of relentless Big Pharma Lobby pressure on corrupt Gov’t & non-existent Health Protection standards. Children as young as 4 have also just been given the green light to receive Psycho-stimulant type drugs for ADD/ADHD. The dystopic nightmare of Brave New World is on our doorstep and not nearly enough of us care either which way to stop it. Please wake up folks! This is not a game.
‘More than one in 10 Americans over the age of 12 takes an antidepressant, a class of drugs that has become wildly popular in the past several decades, U.S. government researchers said Wednesday…Antidepressants were the third-most common drug used by Americans of all ages between 2005 and 2008 and they were the most common drug among people aged 18 to 44, according to an analysis by the U.S. Centers for Disease Control and Prevention’s National Center for Health Statistics.
The team analyzed data on more than 12,000 Americans who took part in the National Health and Nutrition Examination Surveys between 2005 and 2008. They found that antidepressant use in the United States jumped nearly 400 percent in the 2005-2008 survey period compared with the 1988-1994 period, with 11 percent of those over age 12 taking the drugs.’
http://www.reuters.com/article/2011/10/19/us-usa-antidepressants-idUSTRE79I7FI20111019
The zombification of our youngest generation is about to sky-rocket: ‘Children as young as four can be put on psychostimulant drugs for attention deficit disorder, according to new guidelines issued to doctors. The American Academy of Pediatrics released updated guidelines for treating attention-deficit/hyperactivity disorder at its annual conference on the weekend that expand the ages for the diagnosis and treatment of ADHD to preschoolers. “We have already experienced a vast expansion in the diagnosis and medication treatment of ADHD,” renowned U.S. psychiatrist Dr. Allen Frances said in an email. The new guidelines, he said, will encourage “a further feeding frenzy of aggressive marketing by drug companies.”
http://www.vancouversun.com/health/rules+drop+Ritalin+type+drugs/5560458/story.html#ixzz1b5jLYZmG
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BREAKING NEWS: Wild strain of Polio from mass vaccination campaign recently conducted in Pakistan now spreading into China via viral shedding (live virus oral drops method); part of a widespread United Nations managed Eugenics directive targeting the world’s poorest areas
‘A massive vaccination campaign is under way in China after an outbreak of polio, more than 10 years after the country was declared polio free…Children who have been given the vaccine are marked behind the ears with indelible ink to make sure there is no confusion…Vaccination is taking place in homes, kindergartens, schools, bus stations & airports, according to Global Polio Eradication Initiative, which is leading the worldwide effort to wipe out the disease.
Until a few weeks ago, polio was a disease of the past in China, as in most countries around the world. But the discovery of 10 cases of polio in the western province of Xinjiang, and one death, has lead to millions of children and young adults being vaccinated…Genetic studies show the virus came across the border from neighbouring Pakistan.’
http://www.bbc.co.uk/news/health-15095623
Pakistan Launches Massive Polio Vaccination Campaign (July 20, 2011): Health officials in Pakistan are in the middle of a three day nationwide polio eradication campaign throughout the country in an effort to administer anti-polio drops to children under the age of five...Officials have reported that special arrangements have been made to reach 32.7 million children in the country with 39 million doses of polio vaccine. They said that 94,000 special teams have been consulted for the purpose of going door-to-door to administer drops to the children, the Pakistan Observer reports.’
http://vaccinenewsdaily.com/news/254466-pakistan-launches-massive-polio-vaccination-campaign
New widespread Polio outbreak via viral shedding from nasal spray imminent in Somalia: ‘Health-care workers in Somalia today began a 3-day, United Nations-backed campaign to vaccinate more than 1.8 million young children against polio (2 nasal spray doses), 4 years after the Horn of Africa country was declared to be “polio-free”.’ “If we are to ensure that no new cases of polio emerge in Somalia, vaccination teams must be able to access every community, every household & every child aged under five.” Unicef Representative Rozanne Chorlton
http://allafrica.com/stories/201103210007.html
Experimental Type 1 Polio Vaccine live virus drops linked to new outbreak of polio in India: Indian officials are firmly denying any causal link between the sudden death of an infant mere hours after receiving a 5th round dose of Polio Inoculation, part of an additional 2 round dosage of oral drops (Birth, 6 wks, 10 wks, 14 wks, 9-12 months, 18 moths, 2 yrs), despite conclusive evidence of viral shedding & paralytic poliomyelitis associated with the live virus Polio vaccine. ‘The final postmortem report of a two-year-old boy who died hours after receiving oral polio vaccine has categorically established that the cause of death was not the vaccine.’
http://www.thehindu.com/news/states/tamil-nadu/article1700065.ece
‘In 2007 number of (Polio/OPV) vaccination rounds were increased to one round every month, but in 2007 number of polio cases increased further. In 2005 there were 66 polio cases whereas in 2006 and 2007 number of polio cases increased to 676 and 863, respectively. Some mutations in polio viruses may be responsible for development of resistance to antibodies generated by OPV and a reason for the recent steep rise in polio incidence since 2006. Because of these two factors, OPV cannot eradicate polio from India.’
http://www.ncbi.nlm.nih.gov/pubmed/18378367
The Salk & Sabin Polio vaccine spawned a host of hitherto rare/unknown cancers & syndromes including: Mesothelioma (fatal tumor of the membrane surrounding the lungs), Brain cancers (Primarily Ependymomas & Choroid Plexus Tumors, but also Astrocytomas, Glioblastomas, Medulloblastoma, Meningiomas), Bone cancers (Primarily Osteosarcomas, but also Chondrosarcoma & Giant Cell Tumors), Post-Polio Syndrome, Chronic Fatigue Syndrome, Myalgic Encephalomyelitis, Aseptic Meningitis & Non-Hodgkin Lymphoma
See: VRM: Polio – United Nations & The Great Cull
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