Poland GA, Jacobson RM.
Author information
Department of Internal Medicine, Mayo Vaccine Research Group, Mayo Clinic and Foundation, Rochester, MN.
Abstract
BACKGROUND:
Measles is the most transmissible disease known to man. During the 1980s, the number of measles cases in the United States rose dramatically. Surprisingly, 20% to 40% of these cases occurred in persons who had been appropriately immunized against measles. In response, the United States adopted a two-dose universal measles immunization program. We critically examine the effect of vaccine failure in measles occurring in immunized persons.
METHODS:
We performed a computerized bibliographic literature search (National Library of Medicine) for all English-language articles dealing with measles outbreaks. We limited our search to reports of US and Canadian school-based outbreaks of measles, and we spoke with experts to get estimates of vaccine failure rates. In addition, we devised a hypothetical model of a school where measles immunization rates could be varied, vaccine failure rates could be calculated, and the percentage of measles cases occurring in immunized students could be determined.
RESULTS:
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.
CONCLUSIONS:
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.
An investigation into an outbreak in a high school in a town that was heavily hit by the virus found that about half of the cases were in teens who had received the recommended two doses of vaccine in childhood — in other words, teens whom authorities would have expected to have been protected from the measles virus.
It’s generally assumed that the measles vaccine, when given in a two-dose schedule in early childhood, should protect against measles infection about 99 per cent of the time. So the discovery that 52 of the 98 teens who caught measles were fully vaccinated came as a shock to the researchers who conducted the investigation.
“That’s the real question. How could that have happened?” said Dr. Gaston De Serres, an infectious diseases expert with Quebec’s public health agency and one of the authors of the study.
In an interview before the start of the conference, De Serres would not name the highly affected town or the high school in it.
But he suggested the discovery that as many of the cases were fully vaccinated as unvaccinated raises a serious question about whether the timing of the delivery of the first dose of measles vaccine is undermining the efficacy of the prevention program.
The vaccine can’t be given earlier, because of a phenomenon that helps babies survive infancy. Children are born without a fully developed immune system — it starts to build as babies become exposed to a variety of disease threats over their first few years.
In pregnancy and after birth, through breastfeeding, babies acquire antibodies from their mothers that tide them over until they can make their own. But that means if they are given the measles vaccine — which is made from weakened live viruses — too early, their mothers’ antibodies will kill the vaccine viruses, preventing protection from being induced.
US National Library of Medicine
National Institutes of Health – 2006
Abstract
Here we describe symptomatic transmission of the Leningrad-3 mumps vaccine virus from healthy vaccinees to previously vaccinated contacts. Throat swab and serum samples were taken from six symptomatic mumps cases and from 13 family contacts. Assessment of serum IgG and IgM anti-mumps virus antibodies and IgG avidity testing was performed using commercial test kits. Sera neutralizing antibodies were measured by plaque reduction neutralization assay using the L-3 vaccine mumps virus as the target. All six of the symptomatic mumps cases and three contact subjects tested positive for mumps by RT-PCR. The genomic sequences tested (F, SH and HN genes) of all nine of these samples were identical to the L-3 mumps vaccine strain. All 13 contacts were asymptomatic; however clear serological evidence of mumps infection was found in some of them. The likely epidemiological source of the transmitted L-3 mumps virus was children who were recently vaccinated at the schools attended by the six symptomatic mumps patients described here. The L-3 mumps vaccine virus can be shed and transmitted horizontally, even to subjects previously vaccinated with the same virus.
US National Library of Medicine
National Institutes of Health – 2014
Zhifang Wang,1 Rui Yan,1 Hanqing He,1 Qian Li,1 Guohua Chen,2 Shengxu Yang,3 and Enfu Chen1,*
Martyn Kirk, Editor
1 – Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou, Zhejiang Province, P. R. China
2 – Cixi City Center for Disease Control and Prevention, Cixi, Ningbo, P. R. China
3 – Sanmen County Center for Disease Control and Prevention, Sanmen, Taizhou, P. R. China
Abstract
Background
The reported coverage of the measles–rubella (MR) or measles–mumps–rubella (MMR) vaccine is greater than 99.0% in Zhejiang province. However, the incidence of measles, mumps, and rubella remains high. In this study, we assessed MMR seropositivity and disease distribution by age on the basis of the current vaccination program, wherein the first dose of MR is administered at 8 months and the second dose of MMR is administered at 18–24 months.
Methods
Cross-sectional serological surveys of MMR antibodies were conducted by collecting epidemiological data in Zhejiang province, China in 2011. In total, 1015 participants were randomly selected from two surveillance sites. Serum MMR-specific immunoglobulin G levels were tested by enzyme-linked immunosorbent assay. The geometric mean titers and seroprevalence with 95% confidence intervals (CIs) were calculated by age and gender. Proportions of different dose of vaccine by age by vaccine were also identified. Statistically significant differences between categories were assessed by the Chi-square test.
Results
Over 95% seroprevalence rates of measles were seen in all age groups except <7 months infants. Children aged 5–9 years were shown lower seropositivity rates of mumps while elder adolescences and young adults were presented lower rubella seroprevalence. Especially, rubella seropositivity was significantly lower in female adults than in male. Nine measles cases were unvaccinated or unknown vaccination history. Among them, 66.67% (6/9) patients were aged 20–29 years while 33.33% (3/9) were infants aged 8–12 months. In addition, 57.75% (648/1122) patients with mumps were children aged 5–9 years, and 50.54% (94/186) rubella cases were aged 15–39 years.
Conclusions
A timely two-dose MMR vaccination schedule is recommended, with the first dose at 8 months and the second dose at 18–24 months. An MR vaccination speed-up campaign may be necessary for elder adolescents and young adults, particularly young females.
I am injured by the flu shot
MMR vaccine injured me
My family is injured by vaccines
Hep B vaccine and Vit K made my baby sick
I Wish We Would Have KNOWN! William and Rachael tell their story of their two boys who have suffered from vaccine injury in Ireland.
Interview recorded on May 5th, 2017 in The United Kingdom
I have finally woken up to the truth about vaccines
1 Corinthians 15 Authorized (King James) Version (AKJV)
1 Moreover, brethren, I declare unto you the gospel which I preached unto you, which also ye have received, and wherein ye stand;
2 by which also ye are saved, if ye keep in memory what I preached unto you, unless ye have believed in vain.
3 For I delivered unto you first of all that which I also received, how that Christ died for our sins according to the scriptures;
4 and that he was buried, and that he rose again the third day according to the scriptures:
Hebrews 6 Authorized (King James) Version (AKJV)
1 Therefore leaving the principles of the doctrine of Christ, let us go on unto perfection; not laying again the foundation of repentance from dead works, and of faith toward God,
2 of the doctrine of baptisms, and of laying on of hands, and of resurrection of the dead, and of eternal judgment.
3 And this will we do, if God permit.
4 For it is impossible for those who were once enlightened, and have tasted of the heavenly gift, and were made partakers of the Holy Ghost,
5 and have tasted the good word of God, and the powers of the world to come,
6 if they shall fall away, to renew them again unto repentance; seeing they crucify to themselves the Son of God afresh, and put him to an open shame.
7 For the earth which drinketh in the rain that cometh oft upon it, and bringeth forth herbs meet for them by whom it is dressed, receiveth blessing from God:
8 but that which beareth thorns and briers is rejected, and is nigh unto cursing; whose end is to be burned.
Tomljenovic L, Shaw CA.
Author information
Neural Dynamics Research Group, Department of Ophthalmology and Visual Sciences, University of British Columbia, Vancouver, BC, V5Z 1L8, Canada. lucijat77@gmail.com
Abstract
Aluminum is an experimentally demonstrated neurotoxin and the most commonly used vaccine adjuvant. Despite almost 90 years of widespread use of aluminum adjuvants, medical science’s understanding about their mechanisms of action is still remarkably poor. There is also a concerning scarcity of data on toxicology and pharmacokinetics of these compounds. In spite of this, the notion that aluminum in vaccines is safe appears to be widely accepted. Experimental research, however, clearly shows that aluminum adjuvants have a potential to induce serious immunological disorders in humans. In particular, aluminum in adjuvant form carries a risk for autoimmunity, long-term brain inflammation and associated neurological complications and may thus have profound and widespread adverse health consequences. In our opinion, the possibility that vaccine benefits may have been overrated and the risk of potential adverse effects underestimated, has not been rigorously evaluated in the medical and scientific community. We hope that the present paper will provide a framework for a much needed and long overdue assessment of this highly contentious medical issue.
A study published in the Journal Cell Biology and Toxicology by Kinki University in Osaka, Japan determined that in combination with the brain pathology observed in patients diagnosed with autism, the present study helps to support the possible biological plausibility for how low-dose exposure to mercury from thimerosal-containing vaccines may be associated with autism.
US National Library of Medicine
National Institutes of Health – Apr 2010
Minami T, Miyata E, Sakamoto Y, Yamazaki H, Ichida S.
Author information
Department of Life Sciences, Kinki University, Higashi-osaka, Osaka, Japan. minamita@life.kindai.ac.jp
Abstract
Thimerosal, an ethyl mercury compound, is used worldwide as a vaccine preservative. We previously observed that the mercury concentration in mouse brains did not increase with the clinical dose of thimerosal injection, but the concentration increased in the brain after the injection of thimerosal with lipopolysaccharide, even if a low dose of thimerosal was administered. Thimerosal may penetrate the brain, but is undetectable when a clinical dose of thimerosal is injected; therefore, the induction of metallothionein (MT) messenger RNA (mRNA) and protein was observed in the cerebellum and cerebrum of mice after thimerosal injection, as MT is an inducible protein. MT-1 mRNA was expressed at 6 and 9 h in both the cerebrum and cerebellum, but MT-1 mRNA expression in the cerebellum was three times higher than that in the cerebrum after the injection of 12 microg/kg thimerosal. MT-2 mRNA was not expressed until 24 h in both organs. MT-3 mRNA was expressed in the cerebellum from 6 to 15 h after the injection, but not in the cerebrum until 24 h. MT-1 and MT-3 mRNAs were expressed in the cerebellum in a dose-dependent manner. Furthermore, MT-1 protein was detected from 6 to 72 h in the cerebellum after 12 microg/kg of thimerosal was injected and peaked at 10 h. MT-2 was detected in the cerebellum only at 10 h. In the cerebrum, little MT-1 protein was detected at 10 and 24 h, and there were no peaks of MT-2 protein in the cerebrum. In conclusion, MT-1 and MT-3 mRNAs but not MT-2 mRNA are easily expressed in the cerebellum rather than in the cerebrum by the injection of low-dose thimerosal. It is thought that the cerebellum is a sensitive organ against thimerosal. As a result of the present findings, in combination with the brain pathology observed in patients diagnosed with autism, the present study helps to support the possible biological plausibility for how low-dose exposure to mercury from thimerosal-containing vaccines may be associated with autism.
A study published in the Journal Neurochemical Research determined that since excessive accumulation of extracellular glutamate is linked with excitotoxicity, data implies that neonatal exposure to thimerosal-containing vaccines might induce excitotoxic brain injuries, leading to neurodevelopmental disorders.
US National Library of Medicine
National Institutes of Health – Feb 2012
Author information
Michalina Duszczyk-Budhathoki – 1
Mieszko Olczak – 1,3
Malgorzata Lehner – 2
and
Maria Dorota Majewskacorresponding author – 1,4
1 – Marie Curie Chairs Program at the Department of Pharmacology and Physiology of the Nervous System, Institute of Psychiatry and Neurology, 02-957 Warsaw, Poland
2 – Department of Neurochemistry, Institute of Psychiatry and Neurology, 02-957 Warsaw, Poland
3 – Department of Forensic Medicine, Medical University of Warsaw, Oczki 1 str., 02-007 Warsaw, Poland
4 – Department of Biology and Environmental Science, University of Cardinal Stefan Wyszynski, Wóycickiego Str. 1/3, 01-815 Warsaw, Poland Maria Dorota Majewska, Phone: +48-22-45-82-624, Fax: +48-22-45-82-842, Email: moc.liamg@akswejamdm
Abstract
Thimerosal, a mercury-containing vaccine preservative, is a suspected factor in the etiology of neurodevelopmental disorders. We previously showed that its administration to infant rats causes behavioral, neurochemical and neuropathological abnormalities similar to those present in autism. Here we examined, using microdialysis, the effect of thimerosal on extracellular levels of neuroactive amino acids in the rat prefrontal cortex (PFC). Thimerosal administration (4 injections, i.m., 240 μg Hg/kg on postnatal days 7, 9, 11, 15) induced lasting changes in amino acid overflow: an increase of glutamate and aspartate accompanied by a decrease of glycine and alanine; measured 10–14 weeks after the injections. Four injections of thimerosal at a dose of 12.5 μg Hg/kg did not alter glutamate and aspartate concentrations at microdialysis time (but based on thimerosal pharmacokinetics, could have been effective soon after its injection). Application of thimerosal to the PFC in perfusion fluid evoked a rapid increase of glutamate overflow. Coadministration of the neurosteroid, dehydroepiandrosterone sulfate (DHEAS; 80 mg/kg; i.p.) prevented the thimerosal effect on glutamate and aspartate; the steroid alone had no influence on these amino acids. Coapplication of DHEAS with thimerosal in perfusion fluid also blocked the acute action of thimerosal on glutamate. In contrast, DHEAS alone reduced overflow of glycine and alanine, somewhat potentiating the thimerosal effect on these amino acids. Since excessive accumulation of extracellular glutamate is linked with excitotoxicity, our data imply that neonatal exposure to thimerosal-containing vaccines might induce excitotoxic brain injuries, leading to neurodevelopmental disorders. DHEAS may partially protect against mercurials-induced neurotoxicity.
VAXXED TV – Vaccines gave my son seizures
I am vaccine injured and so is my son
My baby is healthy and happy all the time
I’m a dad fighting the system
4 month vaccine injured my baby
James Neuenschwander M.D
He had a lump on his leg for a year A mother shares her observations of her son’s reactions to the vaccines given to him.
Interview recorded on May 5th, 2017 in The United Kingdom
1 Corinthians 15 Authorized (King James) Version (AKJV)
1 Moreover, brethren, I declare unto you the gospel which I preached unto you, which also ye have received, and wherein ye stand;
2 by which also ye are saved, if ye keep in memory what I preached unto you, unless ye have believed in vain.
3 For I delivered unto you first of all that which I also received, how that Christ died for our sins according to the scriptures;
4 and that he was buried, and that he rose again the third day according to the scriptures:
Hebrews 6 Authorized (King James) Version (AKJV)
1 Therefore leaving the principles of the doctrine of Christ, let us go on unto perfection; not laying again the foundation of repentance from dead works, and of faith toward God,
2 of the doctrine of baptisms, and of laying on of hands, and of resurrection of the dead, and of eternal judgment.
3 And this will we do, if God permit.
4 For it is impossible for those who were once enlightened, and have tasted of the heavenly gift, and were made partakers of the Holy Ghost,
5 and have tasted the good word of God, and the powers of the world to come,
6 if they shall fall away, to renew them again unto repentance; seeing they crucify to themselves the Son of God afresh, and put him to an open shame.
7 For the earth which drinketh in the rain that cometh oft upon it, and bringeth forth herbs meet for them by whom it is dressed, receiveth blessing from God:
8 but that which beareth thorns and briers is rejected, and is nigh unto cursing; whose end is to be burned.
A study published in the Journal of Toxicology and Environmental Health determined that mercury exposure can induce immune, sensory, neurological, motor and behavioural dysfunctions similar to traits defining or associated with ASDs. Based upon differential diagnoses, 8 of 9 patients examined were exposed to significant mercury from Thimerosal-containing vaccine preparations during their fetal/infant developmental periods. These previously normal developing children suffered mercury encephalopathies that manifested with clinical symptoms consistent with regressive ASDs. Evidence for mercury intoxication should be considered in the differential diagnosis as contributing to some regressive ASDs.
US National Library of Medicine
National Institutes of Health – May 2007
Geier DA, Geier MR.
Author information
Institute of Chronic Illnesses, Inc., Silver Spring, Maryland, USA.
Abstract
Impairments in social relatedness and communication, repetitive behaviors, and stereotypic abnormal movement patterns characterize autism spectrum disorders (ASDs). It is clear that while genetic factors are important to the pathogenesis of ASDs, mercury exposure can induce immune, sensory, neurological, motor, and behavioral dysfunctions similar to traits defining or associated with ASDs. The Institutional Review Board of the Institute for Chronic Illnesses (Office for Human Research Protections, U.S. Department of Health and Human Services, IRB number IRB00005375) approved the present study. A case series of nine patients who presented to the Genetic Centers of America for a genetic/developmental evaluation are discussed. Eight of nine patients (one patient was found to have an ASD due to Rett’s syndrome) (a) had regressive ASDs; (b) had elevated levels of androgens; (c) excreted significant amounts of mercury post chelation challenge; (d) had biochemical evidence of decreased function in their glutathione pathways; (e) had no known significant mercury exposure except from Thimerosal-containing vaccines/Rho(D)-immune globulin preparations; and (f) had alternate causes for their regressive ASDs ruled out. There was a significant dose-response relationship between the severity of the regressive ASDs observed and the total mercury dose children received from Thimerosal-containing vaccines/Rho (D)-immune globulin preparations. Based upon differential diagnoses, 8 of 9 patients examined were exposed to significant mercury from Thimerosal-containing biologic/vaccine preparations during their fetal/infant developmental periods, and subsequently, between 12 and 24 mo of age, these previously normally developing children suffered mercury toxic encephalopathies that manifested with clinical symptoms consistent with regressive ASDs. Evidence for mercury intoxication should be considered in the differential diagnosis as contributing to some regressive ASDs.
A study conducted by the Department of Obstetrics and Gynaecology at University of Pittsburgh’s School of Medicine showed that Macaques are commonly used in pre-clinical vaccine safety testing. Collective Evolution does not support animals testing, we feel there is a large amount of evidence and research that already indicated the links to vaccines in which some animals have been used to illustrate. The objective of this study was to compare early infant cognition and behaviour with amygdala size and opioid binding in rhesus macaques receiving the recommended childhood vaccines. The animal model, which examines for the first time, behavioural, functional and neuromorphometric consequences of the childhood vaccine regimen, mimics certain neurological abnormalities of autism. These findings raise important safety issues while providing a potential model for examining aspects of causation and disease pathogenesis in acquired disorders of behaviour and development.
Author information
Laura Hewitson – 1,2,*, Brian J. Lopresti – 3, Carol Stott – 4, N. Scott Mason – 3 and Jaime Tomko – 1
1 Department of Obstetrics and Gynecology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA;
2 Thoughtful House Center for Children, Austin, TX, USA;
3 Department of Radiology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA;
4 Independent Chartered Scientist, Cambridge, UK;
Abstract
This longitudinal, case-control pilot study examined amygdala growth in rhesus macaque infants receiving the complete US childhood vaccine schedule (1994-1999). Longitudinal structural and functional neuroimaging was undertaken to examine central effects of the vaccine regimen on the developing brain. Vaccine-exposed and saline-injected control infants underwent MRI and PET imaging at approximately 4 and 6 months of age, representing two specific timeframes within the vaccination schedule. Volumetric analyses showed that exposed animals did not undergo the maturational changes over time in amygdala volume that was observed in unexposed animals. After controlling for left amygdala volume, the binding of the opioid antagonist [11C]diprenorphine (DPN) in exposed animals remained relatively constant over time, compared with unexposed animals, in which a significant decrease in [11C]DPN binding occurred. These results suggest that maturational changes in amygdala volume and the binding capacity of [11C]DPN in the amygdala was significantly altered in infant macaques receiving the vaccine schedule. The macaque infant is a relevant animal model in which to investigate specific environmental exposures and structural/functional neuroimaging during neurodevelopment.
A study conducted by The George Washington University School of Public Health from the Department of Epidemiology and Biostatistics determined that significantly increased rate ratios were observed for autism and autism spectrum disorders as a result of exposure to mercury from Thimerosal-containing vaccines.
US National Library of Medicine
National Institutes of Health – Aug 2008
Young HA, Geier DA, Geier MR.
Author information
The George Washington University School of Public Health and Health Services, Department of Epidemiology and Biostatistics, United States.
Abstract
The study evaluated possible associations between neurodevelopmental disorders (NDs) and exposure to mercury (Hg) from Thimerosal-containing vaccines (TCVs) by examining the automated Vaccine Safety Datalink (VSD). A total of 278,624 subjects were identified in birth cohorts from 1990-1996 that had received their first oral polio vaccination by 3 months of age in the VSD. The birth cohort prevalence rate of medically diagnosed International Classification of Disease, 9th revision (ICD-9) specific NDs and control outcomes were calculated. Exposures to Hg from TCVs were calculated by birth cohort for specific exposure windows from birth-7 months and birth-13 months of age. Poisson regression analysis was used to model the association between the prevalence of outcomes and Hg doses from TCVs. Consistent significantly increased rate ratios were observed for autism, autism spectrum disorders, tics, attention deficit disorder, and emotional disturbances with Hg exposure from TCVs. By contrast, none of the control outcomes had significantly increased rate ratios with Hg exposure from TCVs. Routine childhood vaccination should be continued to help reduce the morbidity and mortality associated with infectious diseases, but efforts should be undertaken to remove Hg from vaccines. Additional studies should be conducted to further evaluate the relationship between Hg exposure and NDs.
VAXXED TV – My Vaxxed child versus my unvaccinated child
1 Corinthians 15 Authorized (King James) Version (AKJV)
1 Moreover, brethren, I declare unto you the gospel which I preached unto you, which also ye have received, and wherein ye stand;
2 by which also ye are saved, if ye keep in memory what I preached unto you, unless ye have believed in vain.
3 For I delivered unto you first of all that which I also received, how that Christ died for our sins according to the scriptures;
4 and that he was buried, and that he rose again the third day according to the scriptures:
Hebrews 6 Authorized (King James) Version (AKJV)
1 Therefore leaving the principles of the doctrine of Christ, let us go on unto perfection; not laying again the foundation of repentance from dead works, and of faith toward God,
2 of the doctrine of baptisms, and of laying on of hands, and of resurrection of the dead, and of eternal judgment.
3 And this will we do, if God permit.
4 For it is impossible for those who were once enlightened, and have tasted of the heavenly gift, and were made partakers of the Holy Ghost,
5 and have tasted the good word of God, and the powers of the world to come,
6 if they shall fall away, to renew them again unto repentance; seeing they crucify to themselves the Son of God afresh, and put him to an open shame.
7 For the earth which drinketh in the rain that cometh oft upon it, and bringeth forth herbs meet for them by whom it is dressed, receiveth blessing from God:
8 but that which beareth thorns and briers is rejected, and is nigh unto cursing; whose end is to be burned.
Désirée Röver – Vaccines, Part 1
By OLE DAMMEGARD June 10, 2017
Ole Dammegård interviews Medical Research Journalist Désirée Röver from the Netherlands, about vaccines and the dangers involved. What started her painful journey of discovery into this dark world was the death of her 2 year old son, due to a vaccination.
Brittney Kara encourages parents to do their research before allowing toxic vaccines to be injected into their children. Start your research by watching Vaccines Revealed featuring 24 vaccine experts by clicking here http://bit.ly/2o0b5Cp and go to http://www.stopmandatoryvaccination.com/personal-choice/ to read Brittney’s vaccine free overview.
Medical Doctor who Escaped Vietnam as a Child in the 1970s Explains Why He no Longer Vaccinates
The VAXXED film crew recently interviewed Dr. Anthony Phan in California. Dr. Phan escaped from Vietnam in the 1970s when he was 8 years old. He was separated from his parents and escaped on a fishing boat along with his 2 year old brother.
Making it to the U.S. as a child refugee, Dr. Phan testifies that God led him through college and medical school, and he went on to become a medical doctor at Johns Hopkins.
Dr. Phan talks about how his mentor at Johns Hopkins taught him about the importance of the Hippocratic Oath to “do no harm.”
Do no harm means your oath is to the patient. Not to the CDC, not to the government, not to the FDA, your oath is to the patient.
His mentor also reportedly stated to him:
One day Tony, in your career (this was in 1993), when you see these threesome (CDC, FDA, and the government) in bed together, be very careful. When you see pharmaceutical companies being in bed with the government, and being controlled by the health industry, you need to make a decision about where you want to take your medical career.
Either #1 you retire and get out, because it is back to being controlled again, back to where I escaped (from Vietnam) in 1975.
Dr. Phan explains that his experience with vaccines began in 2000 when he did his fellowship in Integrated Medicine. He was taught to question the practices of “conventional” medicine that are wrong.
THOUSANDS protest in numerous cities across Italy in what is now an INTERNATIONAL️ uprising and Revolution for Choice!
What haven’t you been told? Find out now for free: tiny.cc/FreeVaccinationEducation
Networking, exemption information and doctor resources: tinyurl.com/RevolutionForVaccineChoice
Follow us: facebook.com/RevolutionForChoice #RevolutionForChoice #InformedConsent #EducateBeforeYouVaccinate #VAXXED #Italy #VaccineInjury #NonCompliance #RiseUP
Learn OUR NAMES!!! Our international battle for medical choice and parental choice is only getting started! Join our movement of people who have done their research! . . . Click here to obtain the information you need to make the most informed choices for your yourself and your family >>> tinyurl.com/9Episodes
✴️ Translation courtesy of Teresa Iodice ️
✴️ Networking, exemption information and doctor resources: tinyurl.com/RevolutionForVaccineChoice
✴️ Follow us: facebook.com/RevolutionForChoice
✴️ Read all vaccine inserts: tinyurl.com/ReadTheVaccineInsert #RevolutionForChoice #InformedConsent #EducateBeforeYouVaccinate #VAXXED #SB277 #RiseUp #Italy #Rome #Naples
Dirty Vaccines: New Study Reveals Prevalence of Contaminants
Posted by Celeste McGovern on Jan 30, 2017 5:31:20 PM
Every Human Vaccine Tested Was Contaminated by Unsafe Levels of Metals and Debris Linked to Cancer and Autoimmune Disease, New Study Reports
Researchers examining 44 samples of 30 different vaccines found dangerous contaminants, including red blood cells in one vaccine and metal toxicants in every single sample tested – except in one animal vaccine.
Using extremely sensitive new technologies not used in vaccine manufacturing, Italian scientists reported they were “baffled” by their discoveries which included single particles and aggregates of organic debris including red cells of human or possibly animal origin and metals including lead, tungsten, gold, and chromium, that have been linked to autoimmune disease and leukemia.
In the study, published this week in the International Journal of Vaccines and Vaccination, the researchers led by Antonietta Gatti, of the National Council of Research of Italy and the Scientific Director of Nanodiagnostics, say their results “show the presence of micro- and nano-sized particulate matter composed of inorganic elements in vaccine samples” not declared in the products’ ingredients lists.
Lead particles were found in the cervical cancer vaccines, Gardasil and Cervarix, for example, and in the seasonal flu vaccine Aggripal manufactured by Novartis as well as in the Meningetec vaccine meant to protect against meningitis C.
Samples of an infant vaccine called Infarix Hexa (against diphtheria, tetanus, pertussis, hepatitis B, poliomyelitis and haemophilus influenzae type B) manufactured by GlaxoSmithKline was found to contain stainless steel, tungsten and a gold-zinc aggregate.
Other metal contaminants included platinum, silver, bismuth, iron, and chromium. Chromium (alone or in alloy with iron and nickel) was identified in 25 of the human vaccines from Italy and France that were tested.
GSK’s Fluarix vaccine for children three years and older contained 11 metals and aggregates of metals. Similar aggregates to those identified in the vaccines have been shown to be prevalent in cases of leukemia, the researchers noted.
1. I understand that the pharmaceutical company who made this vaccine has NO liability if it injures or kills my child.
2. If my child is killed or hurt by a vaccine, the public will pay through increased taxes for any damage the vaccine does and in Canada it’s very little payment for a dead or injured child.
3. I understand that these vaccines contains neurotoxins such as aluminum and mercury that far exceed “safe levels” deemed by the EPA.
4. I understand that these vaccines contain carcinogenic ingredients PROVEN to cause CANCER.
5. I understand that some vaccines are made from aborted fetal cell lines, of both humans and animals and their DNA is INJECTED into you and your child along with everything else (including an adjuvant that tells your immune system to attack EVERYTHING in the vaccine, INCLUDING HUMAN CELLS.)
6. I understand that getting this vaccine does not ensure that I will be protected from the disease. Many OUTBREAKS include a Population of 100% vaccinated individuals.
Patients with an Allergy to Eggs Are at Risk of Anaphylaxis from MMR Vaccine
Posted on: Wednesday, February 1st 2017 at 10:30 am
Written By: Christina England, BA Hons
According to the National Institute of Allergy and Infectious Diseases Patients with an Allergy to Eggs Are at Risk of Anaphylaxis if Vaccinated with the MMR!
It is estimated that up to 15 million US citizens are currently suffering from food allergies. In 2013, a paper published on the CDC website stated that between 1997 and 2011, the prevalence of food and skin allergies increased in children under age of 18. This is extremely worrying, as according to the Food Allergy Research & Education website, a food allergy sends someone to the emergency department every three minutes, which, according to them, amounts to approximately 200,000 visits to the ER every year.
The NIAID Recommend the MMR to Children with Egg Allergies
In 2010, the National Institute of Allergy and Infectious Diseases (NIAID) published a paper titled Guidelines for the Diagnosis and Management of Food Allergy in the United States. The paper described how the NIAID had joined forces with 30 professional organizations, federal agencies and patient advocacy groups to set guidelines for the management and safety of patients suffering from food allergies.
One of the sections highlighted was a section titled Vaccinations in Patients with Egg Allergies.’ The authors wrote:
“In Summary: Patients who have generated IgE antibodies to an allergen are at risk for anaphylaxis with systemic exposure to that allergen. Thus, patients who have IgE-mediated egg allergy are at risk for anaphylaxis if injected with vaccines containing egg 17 protein.” (own emphasis)
They continued:
“More detailed information about specific egg-containing vaccines (measles, mumps, and rubella [MMR], MMR with varicella [MMRV], influenza, yellow fever, and rabies) is provided in … the Guidelines.
The EP recognizes that changes in these recommendations may occur in the future as there is an increased understanding of the risk factors for allergic reactions and as vaccine manufacturing processes improve and decrease the final egg protein content of vaccines. For the most current recommendations, health care professionals should refer to the Web sites of the American Academy of Pediatrics (AAP) and Advisory Committee for Immunization Practices (ACIP): http://aapredbook.aappublications.org/ http://www.cdc.gov/vaccines/recs/acip/
However, despite stating that patients who have an allergy to eggs are at risk of anaphylaxis if they receive a vaccine containing the egg 17 protein, it appears that they are recommending the vaccine anyway.
I say this, because in section 5.1.11.1 they stated:
“Measles, Mumps, Rubella, and Varicella Vaccine
Guideline 31: The EP recognizes the varying consensus recommendations of the different organizations on this particular vaccine and recommends that children with egg allergy, even those with a history of severe reactions, receive vaccines for MMR and MMRV. The safety of this practice has been recognized by ACIP and AAP and is noted in the approved product prescribing information for these vaccines.” (own emphasis)
What I found interesting was the fact that the NIAID did not apply the same guidelines to any of the other vaccinations listed.
In fact, their recommendations for the flu vaccine clearly stated:
“In Summary: The EP concludes that insufficient evidence exists to recommend administering influenza vaccine, either inactivated or live-attenuated, to patients with a history of severe reactions to egg proteins. Severe reactions include a history of hives, angioedema, allergic asthma, or systemic anaphylaxis to egg proteins (or chicken proteins). Less severe or local manifestations of allergy to egg or feathers are not contraindications. However, the EP notes that egg allergy is relatively common among the very patients who would highly benefit from influenza vaccination. Such patients include children and young adults (from 6 months to 18 years old for seasonal influenza, and from 6 months to 24 years old for H1N1 influenza) and all patients with asthma. It should be noted that live-attenuated vaccine is not licensed for use in patients with asthma.” (own emphasis)
They continued:
“Although ACIP and AAP, and also the vaccine manufacturers, do not recommend influenza vaccination in patients who are allergic to egg, several publications have described different approaches to giving the influenza vaccine to patients with severe allergic reactions to egg. These approaches, which depend on the ovalbumin content and the results of SPTs or intradermal tests with the vaccine, include a single dose of vaccine, two doses of vaccine, or multiple doses. However, the evidence supporting these approaches is limited by the small numbers of patients included in each study. Moreover, data indicate that, although the vaccines are relatively safe, there remains some, albeit low, risk of systemic reactions. Also, negative SPT results do not accurately predict safety of vaccination, in that 5 percent of patients with negative SPTs had systemic reactions to vaccination.” (own emphasis)
With these recommendations in mind, we need to ask ourselves how many of our doctors are fully aware of any of these guidelines? If they are aware of this information, why are so many doctors not adhering to them?
13 Year-Old Boy Permanently Disabled from Chicken Pox Vaccine Wins His Case in Vaccine Court
A young man was recently awarded compensation in the United States Court of Federal Claims Vaccine Court, for injuries he sustained after being administered the hepatitis A and varicella vaccinations in 2009. After five long years of litigation, Health and Human Services (HHS), the Respondent in all vaccine injury cases, conceded that the varicella vaccination did in fact cause RD’s vaccine injury, transverse myelitis, which has left him a tetraplegic.
In November 2014, HHS conceded that the vaccination caused RD’s injuries. Even with this concession, his case continued for another year in the damages phase, during which time the parties continued to negotiate the amount of damages that RD would receive for his injuries. Although he was compensated for his suffering and injuries, the monetary award will never compensate for the lifelong effects this young man is suffering from his vaccine injury.
Five Long Years
RD was only 13 when his life changed forever. At a routine well-child visit in 2009, the doctor informed RD’s parents that he was due to receive the hepatitis A and varicella vaccinations. His parents complied with the doctor’s order and RD received the vaccinations.
RD’s mother explained that, at that time in RD’s state, only one dose of varicella vaccine was required and RD had already received one dose of that vaccine. This second dose that was administered to RD at this well visit was determined to be the cause of RD’s horrific injuries, and it was not even required for him, which his family didn’t realize until it was too late.
About 14 days later, RD began to experience excruciating pain shooting through his body along with tingling, numbness and paralysis of his limbs. After extensive testing and many invasive procedures, RD was diagnosed with transverse myelitis.
RD’s parents filed a case in Vaccine Court, which took over five years to settle. RD and his family faced arduous heartbreak along the way. In the ruling, a representative from the United States Department of Justice agreed that “a preponderance of the evidence establishes that petitioner’s transverse myelitis was caused-in-fact by the administration of his August 12, 2009 varicella vaccine.” [1]
RD’s lawyer, Patricia Finn, stated that:
“The injuries that RD suffered from this vaccine are severe and lifelong. Even though he has received a significant award as far as the awards in the Vaccine Court go, no amount of money will ever compensate him for what he has lost.
But RD is an amazing young man who has not let this injury stop him in any way. He has graduated high school with his class, attends a Tier 1 college, and has great aspirations that I know he will achieve despite the challenges he faces because of his injuries.”
RD’s Immune System Attacked His Spine
Autism vs. Childhood Diseases: Breaking Down The Walls Of Pro-Vaccine Ignorance
By Tami Canal On June 19, 2017
I can’t tell you how absolutely fed up I am with tragically misinformed people who proclaim that they would prefer to have an autistic child versus one with a case of the measles, mumps, chicken pox, etc.
A comment like that demonstrates immense ignorance in regards to the LIFETIME of issues that autism presents–things like social dysfunction, the inability to speak, aggression, self-destructive behavior, and a staggeringly diminished life expectancy. If you are one of the people who have ever believed measles or other infectious diseases to be worse than autism, this is for you.
Let’s take a look and examine these so-called “deadly” childhood diseases.
1. Chicken Pox (Varicella) = itchy rash with small fluid-filled blisters; 5-7 days of feeling tired and sluggish; mild fever; decreased appetite. Resolves itself.
2. Diptheria = low fever, sore throat, croup-like cough; many infections are asymptomatic or mild. Treat with antitoxin and antibiotics. Garlic juice and table salt are natural remedies to successfully treat diphtheria, as well.
3. Haemophilus influenzae Type B (Hib) = flu symptoms, stiff neck, lethargy. Treat with antibiotics for 10 days.
4. Hepatitis A = transmitted by eating food or drinking water contaminated with feces; children usually have no symptoms; when symptoms occur, they include flu-like symptoms, nausea, jaundice. Resolves itself.
5. Hepatitis B = transmitted through blood, semen, vaginal fluids; flu-like symptoms, dark urine, vomiting, jaundice; most people do not show symptoms. Acute Hep B resolves itself.
6. Human Papilloma Virus (HPV) = transmitted sexually; usually resolves itself with no symptoms; takes years to develop into cancer; regular pap screens prevent cancer; vaccine discontinued in Japan due to adverse reactions.
7. Influenza (flu) = high fever, cold symptoms, vomiting; lasts 7-10 days; Resolves itself. (Flu vaccine contains mercury [thimerosal]).
8. Measles = fever, cold symptoms, rash; 7-10 days; Resolves itself. Infection can be avoided with proper nutrition, primarily adequate levels of Vitamin A and C.
9. Meningitis = flu symptoms, stiff neck; usually caused by bacteria or virus; viral usually causes no symptoms and resolves itself; bacterial is spread through saliva (kissing, coughing); Most people who ‘carry’ the bacteria never become sick; bacterial meningitis is treated with antibiotics.
10. Mumps = fever, swelling of salivary glands; many people show no symptoms; Resolves itself within a few weeks. (There are many effective natural home remedies for mumps which are safe and provide relief from pain without any harmful side effects.)
11. Pertussis (whooping cough) = dry cough, watery eyes, slight fever, lethargy; treated with high doses of vitamin C; garlic, almond oil, honey, and onion are also effective, natural remedies to treat pertussis.
12. Pneumococcal Pneumonia = flu-like symptoms, fatigue, chills, stiff neck; Treated with antibiotics.
13. Poliomyelitis = 72% of infections cause no symptoms; 25% flu-like symptoms that last 2-5 days; 0.5% leads to more severe symptoms such as paralytic polio; only people with the paralytic infection are considered to have the disease. It is noteworthy to mention that a congressional hearing in the 1950s shed light that polio was actually the result of DDT poisoning and that the federal government and the chemical industry fabricated polio to conceal the true cause of paralysis-inducing epidemic sweeping the country. (Read more about polio here.)
14. Rotavirus = infection in the intestinal tract that causes vomiting, diarrhea, and dehydration; Children, even those that are vaccinated for rotavirus, may develop the disease more than once. A diet high in potassium, such as BRAT, will help bind the bowels and can greatly alleviate the symptoms of Rotavirus. Other natural remedies can be found here.
15. Rubella (German measles) = flu-like symptoms, swollen lymph nodes, joint pain, fatigue, rash; 1-3 days; 25 to 50% of people infected with rubella will not experience any symptoms. Resolves itself. Turmeric, licorice, and citrus are highly effective home remedies.
16. Tetanus = sudden, painful contractions of muscle groups; caused by Clostridium tetani transmitted through broken skin; Prevention is to allow wound to bleed freely. Tetanus bacteria is anaerobic – meaning oxygen will kill it.
Dr. Andrew Moulden: Every Vaccine Produces Microvascular Damage
by John P. Thomas
Health Impact News
Dr. Andrew Moulden recognized that every dose of vaccine given to a person produced microvascular damage whether or not the person was aware of the damage or had debilitating symptoms at the time the vaccines were given. He courageously stepped out of the conventional box of medical diagnosis and treatment, and gave us a new way to look at modern neurodevelopmental illnesses and syndromes.
This series of articles is intended to preserve the work of Dr. Moulden, who unexpectedly died in November of 2013. I want to acknowledge the contribution of this forward-thinking pioneer who worked to explain the truth about vaccine damage. This is article two in a series of four articles about Dr. Moulden’s life work.
As a physician and PhD researcher, he raised strong public objection to vaccine use, because he could literally see evidence of vaccine damage in the expressions of the human face. Each dose of a vaccine causes tiny strokes in the brain and in other organs of the body, which bring about a wide range of unexpected health conditions.
Dr. Moulden saw that the rapid rise in modern neurodevelopmental diseases such as autism, Alzheimer’s, and numerous other syndromes were actually caused by the same process. He saw the current epidemic of these modern diseases as having a single origin. The notion of single diseases with single causes had to be put aside, because that model could not adequately explain what we are facing in the world today.
How Vaccines and Toxins Producing a Syndrome of Closely Related Illnesses
Dr. Moulden understood that vaccines and toxins (in the air, in our water, in our homes, and in our food) were producing a syndrome of closely related illnesses. He said that it was time to begin thinking in terms of multiple causes for a syndrome that had multiple sets of symptoms.
Multiple factors can work together to trigger a single type of reaction in the body, which can then produce various sets of symptoms. Even though there were different sets of symptoms and different disease names given to each one, they were actually all part of a spectrum of diseases that he called Moulden Anoxia Spectrum Syndromes.
Learning disabilities, autism, Alzheimer’s, irritable bowel disease, Crohn’s disease, colitis, food allergies, shaken baby syndrome, sudden infant death, idiopathic seizure disorders, Gulf War syndrome, Gardasil adverse reactions, schizophrenia, Tourette’s syndrome, chronic fatigue syndrome, fibromyalgia, expressive aphasia, impaired speech skills, attention deficit disorders, silent ischemic strokes, blood clots, idiopathic thrombocytopenia purpura, Parkinson’s disease, and other modern neurodevelopmental disorders are closely related in many ways, and are part of a larger syndrome.
Study – Oxidative Stress and NAD+ in Ischemic Brain Injury: Current Advances and Future Perspectives
Abstract
Numerous studies have indicated oxidative stress as a key pathological factor in ischemic brain injury. One of the key links between oxidative stress and cell death is excessive activation of poly(ADP-ribose) polymerase-1 (PARP-1), which plays an important role in the ischemic brain damage in male animals. Multiple studies have also suggested that NAD+ depletion mediates PARP-1 cytotoxicity, and NAD+ administration can decrease ischemic brain injury.
A number of recent studies have provided novel information regarding the mechanisms underlying the roles of oxidative stress and NAD+-dependent enzymes in ischemic brain injury. Of particular interest, there have been exciting progresses regarding the mechanisms underlying the roles of NADPH oxidase and PARP-1 in cerebral ischemia. For examples, it has been suggested that androgen signaling and binding of PARP-1 onto estrogen receptors could account for the intriguing findings that PARP-1 plays remarkably differential roles in the ischemic brain damage of male and female animals; and some studies have suggested casein kinase 2, copper-zinc superoxide dismutase, and estrogen signaling can modulate the expression and activity of NADPH oxidase.
This review summarizes these important current advances, and proposes future perspectives for the studies on the roles of oxidative stress and NAD+ in cerebral ischemia. It is increasingly likely that future studies on NAD- and NADP-dependent enzymes, such as NADPH oxidase, PARP-1, and sirtuins, would expose novel mechanisms underlying the roles of oxidative stress in cerebral ischemia, and suggest new therapeutic strategies for treating the debilitating disease.
Natural News – Gardasil, considered the most dangerous vaccine on the market, may soon be pushed for infants
Wednesday, November 23, 2016 by: Vicki Batts
(NaturalNews) Gardasil has been the subject of controversy for many years now. In fact, it has even been regarded as one of the most dangerous vaccines on the market today. Perhaps what is most alarming about this treacherous vaccine, however, is the fact that its manufacturer, Merck & Co, now wants to begin marketing their product to infants – and trials on babies have already begun. Merck recently launched a Gardasil vaccine trial on children at least one year old, and it’s set to conclude in early 2017.
You read that right. A pharmaceutical giant is testing a vaccine for an STD on babies. It doesn’t really get more corrupt and outrageous than that, now does it?
Gardasil was developed for the STD known as HPV, and was approved by the FDA in 2006. The disease did not become of concern until the 1980s, when research first suggested that there may be a link between HPV and cervical cancer. However, whether this link actually exists has been a major point of contention. There are several hypotheses that explain why HPV may not actually cause cancer, but one particularly interesting theory was expressed by McCormack et al in their paper published by the journal Molecular Cytogenetics in 2015. The research team also raised several significant questions about the prevailing theory on the connection between HPV and cervical cancer. For example, HPV is present in 70 to 80 percent of the American adult population, so why does cervical cancer only effect one out of ever 10,000 women?
According to their paper, neither HPV nor genetic predisposition is required for the onset of cervical cancer. In fact, all of the cervical cancer cells analyzed during the course of their study contained new abnormal karyotypes. The genetic makeup of these new abnormal karyotypes suggested that the cervical cancers originated within the karyotypes, and not from a virus. A karyotype is the size, number and shape of chromosomes within an organism. Their theory, called the Karyotypic Speciation Theory, essentially suggests that “carcinomas are generated de novo from cellular chromosomes, genes and proteins, which are not immunogenic in the host of origin (just like all other cancers).” As SaneVax.org explains, in this theory, hypothetical cancer cells that are generated by viral proteins (such as HPV) would be eliminated by antiviral immunity.
VACCINURILE ȘI AUTOIMUNITATEA – un tratat de imunologie aplicată echilibrat; rezultatul zecilor de ani de experiență în vaccinologie și autoimunitate și a studierii unei cazuistici și literaturi de specialitate extrem de vaste, are 37 de capitole și exprimă un adevăr dramatic: o parte dintre oamenii sănătoși (despre care nu știm dacă s-ar fi îmbolnăvit vreodată) fac boli autoimune după și prin administrarea unui vaccin: lupus, vasculite, artrită reumatoidă, boli de țesut conjunctiv nediferențiate, purpură trombocitopenică, boală celiacă ETC.
« Autorii cărții sunt medici specializați în imunologie fundamentală și clinică. Este vorba de o lucrare curajoasă în condițiile vremurilor noastre deoarece trezește un spirit de prudență – altfel destul de amorțit sau bine manipulat – spirit prevazător imperios necesar de vreme ce unele guverne vor să decreteze obligativitatea vaccinării, adică să-și agreseze poporul lor cu o lege totalitară. », Dr. Pavel Chirilă, Prefață la ediția 2016.
Vaccine injury testimony – vit K injured my child #vaxxed #PrayBig #RFKcommission
Why did the media stop talking about Hannah Poling? Easy: her case of vaccines causing autism was unassailable. Her dad was a neurologist. They’d won big in vaccine court. Even the head of CDC, Julie Gerberding, had to concede that autism happened in rare cases. Then what happened? The Polings, and Hannah’s story, simply disappeared from the media. It was too devastating a blow, so just pretend it never happened. Thank God for YouTube!! (Also, remember: Mary Holland and others found 83 cases in Vaccine Court exactly like Hannah Poling–it’s not as rare as Dr. Gupta makes it out to be see link in the first comment below.)
Vaccine news – Forrest Maready makes a cool thing #vaxxed #PrayBig #RFKcommission
Vaccine news – super healthy unvaccinated children #vaxxed #PrayBig #RFKcommission #unvaxxed
Vaccine injury testimony – #Vaxxed #Twins #VaxxedTwins #Texas
Sunny Irby Polito’s twins, Luke and Campbell, both regressed after receiving MMR and several other vaccinations concurrently at their 12-month “well baby” visit.
“They just blew up in a GI sort of way…12-15 diapers a day for each of them”
#MMR #VaccineInjuryInterviews #CatchupCocktail
#VaxxedNation #VaxxedNationTour #VaxWithMe
#LossOfSpeech #LossOfEyeContact #FineAndGrossMotorSkills #CNSdamage
Editor: Robin Aris
Mum hits out after daughter is given HPV vaccine at school without her consent
By TracyWalker | Posted: February 03, 2017
A concerned mum says she is “upset” that her daughter was given a cervical cancer vaccine at school without parental consent.
Laverne Crosebourne has hit out after her 13-year-old daughter Shian Nichols was given the HPV (Human papilloma virus) jab at Top Valley Academy.
Laverne, of Basford, said she had not wanted her daughter to have the injection, as she has read about possible risks.
But she said her daughter came home from school on Tuesday and said she had been given the vaccination.
the news network 