Wringe A, Fine PE, Sutter RW, Kew OM.
Author information
Department of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, England. alison.wringe@lshtm.ac.uk
Abstract
BACKGROUND:
Eight outbreaks of paralytic polio attributable to circulating vaccine-derived poliovirus (cVDPV) have highlighted the risks associated with oral poliovirus vaccine (OPV) use in areas of low vaccination coverage and poor hygiene. As the Polio Eradication Initiative enters its final stages, it is important to consider the extent to which these viruses spread under different conditions, so that appropriate strategies can be devised to prevent or respond to future cVDPV outbreaks.
METHODS AND FINDINGS:
This paper examines epidemiological (temporal, geographic, age, vaccine history, social group, ascertainment), and virological (type, genetic diversity, virulence) parameters in order to infer the numbers of individuals likely to have been infected in each of these cVDPV outbreaks, and in association with single acute flaccid paralysis (AFP) cases attributable to VDPVs. Although only 114 virologically-confirmed paralytic cases were identified in the eight cVDPV outbreaks, it is likely that a minimum of hundreds of thousands, and more likely several million individuals were infected during these events, and that many thousands more have been infected by VDPV lineages within outbreaks which have escaped detection.
CONCLUSIONS:
Our estimates of the extent of cVDPV circulation suggest widespread transmission in some countries, as might be expected from endemic wild poliovirus transmission in these same settings. These methods for inferring extent of infection will be useful in the context of identifying future surveillance needs, planning for OPV cessation and preparing outbreak response plans.
US National Library of Medicine
National Institutes of Health – Mar 2017
Berchenko Y – 1, Manor Y – 2, Freedman LS – 3, Kaliner E – 4, Grotto I – 4,5, Mendelson E – 2,6, Huppert A – 3,6.
Author information
1 Department of Industrial Engineering and Management, Ben-Gurion University of the Negev, P. O. 653, Beer-Sheva 84105, Israel. byakir@gmail.com.
2 Central Virology Laboratory, Ministry of Health, Chaim Sheba Medical Center, Tel Hashomer 52621, Israel.
3 Biostatistics Unit, Gertner Institute for Epidemiology and Health Policy Research, Tel Hashomer 52621, Israel.
4 Public Health Services, Ministry of Health, Jerusalem 9101002, Israel.
5 Department of Public Health, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva 84105, Israel.
6 School of Public Health, Sackler Faculty of Medicine, Tel Aviv University, P. O. 39040, Tel Aviv 6997801, Israel.
Abstract
A major obstacle to eradicating polio is that poliovirus from endemic countries can be reintroduced to polio-free countries. Environmental surveillance (ES) can detect poliovirus from sewage or wastewaters samples, even in the absence of patients with paralysis. ES is underused, in part because its sensitivity is unknown. We used two unique data sets collected during a natural experiment provided by the 2013 polio outbreak in Israel: ES data from different locations and records of supplemental immunization with the live vaccine. Data from the intersecting population between the two data sets (covering more than 63,000 people) yielded a dose-dependent relationship between the number of poliovirus shedders and the amount of poliovirus in sewage. Using a mixed-effects linear regression analysis of these data, we developed several quantitative tools, such as (i) ascertainment of the number of infected individuals from ES data for application during future epidemics elsewhere, (ii) evaluation of the sensitivity of ES, and (iii) determination of the confidence level of the termination of poliovirus circulation after an outbreak. These results will be valuable in monitoring future outbreaks with ES, and this approach could be used to certify poliovirus elimination or to validate the need for more containment efforts.
US National Library of Medicine
National Institutes of Health – May 2012
Sasaki A, Haraguchi Y, Yoshida H.
Author information
Department of Evolutionary Studies of Biosystems, The Graduate University for Advanced Studies Hayama, Kanagawa, Japan.
Abstract
Live vaccination against polio has effectively prevented outbreaks in most developed countries for more than 40 years, and there remain only a few countries where outbreaks of poliomyelitis by the wild strain still threaten the community. It is expected that worldwide eradication will be eventually achieved through careful surveillance and a well-managed immunization program. The present paper argues, however, that based on a simple stochastic model the risk of outbreak by a vaccine-derived strain after the cessation of vaccination is quite high, even if many years have passed since the last confirmed case. As vaccinated hosts are natural reservoirs for virulent poliovirus, the source of the risk is the vaccination itself, employed to prevent the outbreaks. The crisis after stopping vaccination will emerge when the following two conditions are met: the susceptible host density exceeds the threshold for epidemics and the vaccinated host density remains large enough to ensure the occurrence of virulent mutants in the population. Our estimates for transmission, recovery, and mutation rates, show that the probability of an outbreak of vaccine-derived virulent viruses easily exceeds 90%. Moreover, if a small fraction of hosts have a longer infectious period, as observed in individuals with innate immunodeficiency, the risk of an outbreak rises significantly. Under such conditions, successful global eradication of polio is restricted to a certain range of parameters even if inactivated polio vaccine (IPV) is extensively used after the termination of live vaccination.
VAXXED TV – “Just a Vitamin” – Child with MTHFR Poisoned by Vitamin K Shot at Birth
Nicole was firm in her decision to delay all vaccines, but she was under the common misconception that the Vitamin K shot was, “just a vitamin”. She believes that her now 13 year-old son, Wyatt, was poisoned by the “Vitamin” K shot at birth. The shot now carries a black box warning.
INSULT TO INJURY! – Vaccination of Pre-Term Infants
Dr. Suzanne Humphries will show you medical evidence that sick babies are being made sicker in an uncontrolled experiment.
“It took me 7 years to teach him how to chew”
Nancy Kirkman’s son was severely injured by vaccines at 3 months of age. The family has been subjected to immense heartache and cruelty.
Worst Nightmare for Mother of 6 Unvaxxed Children
The mother of 6 unvaccinated children visits the emergency room with her eldest daughter. Her worst nightmare becomes reality when her child is vaccinated without her consent.
Daughter of a Pediatric Nurse, “I was first in line for my vaccines”
Summer is a holistic health practitioner. Her mother cried when she learned that Summer had stopped vaccinating.
Unvaxxed: Pre-Internet Vaccine Skepticism
Before the internet and smart phone technology gave us anytime anywhere access to medical literature, parent and expert testimony, and thousands of raw files and hours of recorded whistle blower audio, Sherrine Pigott began her vaccine research 32 years ago by reading Dr. Robert Mendelsohn’s book, “How to Raise a Healthy Child in Spite of Your Doctor: One of America’s Leading Pediatricians Puts Parents Back in Control of Their Children’s Health”.
Mother of Vaccine-Injured Son Pregnant with Her Second Child
I Feel Like My Daughter is Victimized Over and Over Again
UnVaxXed Stories: Nursing Student with Unvaccinated Infant
VaxXed Stories: Gardasil Damage and Realization of Previous Vaccine Injury
After her son’s adverse reaction to his vaccinations at 15 years old, which included Gardasil, Jamie started to piece together the negative changes in his health that had occurred with previous rounds of vaccinations. After the vaccinations at 15 years old he developed sensitivity to light, headaches and back pain. His demeanor changed losing ease of communication and critical thinking. He also developed seizures, which they thankfully have been able to control.
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:
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.
1 Who hath believed our report? and to whom is the arm of the Lord revealed?
2 For he shall grow up before him as a tender plant,and as a root out of a dry ground:he hath no form nor comeliness;and when we shall see him,there is no beauty that we should desire him.
3 He is despised and rejected of men;a man of sorrows, and acquainted with grief:and we hid as it were our faces from him;he was despised, and we esteemed him not.
4 Surely he hath borne our griefs,and carried our sorrows:yet we did esteem him stricken,smitten of God, and afflicted.
5 But he was wounded for our transgressions,he was bruised for our iniquities:the chastisement of our peace was upon him;and with his stripes we are healed.
6 All we like sheep have gone astray;we have turned every one to his own way;and the Lord hath laid on him the iniquity of us all.
7 He was oppressed, and he was afflicted,yet he opened not his mouth:he is brought as a lamb to the slaughter,and as a sheep before her shearers is dumb,so he openeth not his mouth.
8 He was taken from prison and from judgment:and who shall declare his generation? for he was cut off out of the land of the living:for the transgression of my people was he stricken.
9 And he made his grave with the wicked,and with the rich in his death;because he had done no violence,neither was any deceit in his mouth.
10 Yet it pleased the Lord to bruise him;he hath put him to grief:when thou shalt make his soul an offering for sin,he shall see his seed, he shall prolong his days,and the pleasure of the Lord shall prosper in his hand.
11 He shall see of the travail of his soul, and shall be satisfied:by his knowledge shall my righteous servant justify many;for he shall bear their iniquities.
12 Therefore will I divide him a portion with the great,and he shall divide the spoil with the strong;because he hath poured out his soul unto death:and he was numbered with the transgressors;and he bare the sin of many,and made intercession for the transgressors.
Tomljenovic L, Shaw CA.
Author information
Neural Dynamics Research Group, Department of Ophthalmology and Visual Sciences, University of British Columbia, Vancouver, BC, Canada. lucijat77@gmail.com
Abstract
Immune challenges during early development, including those vaccine-induced, can lead to permanent detrimental alterations of the brain and immune function. Experimental evidence also shows that simultaneous administration of as little as two to three immune adjuvants can overcome genetic resistance to autoimmunity. In some developed countries, by the time children are 4 to 6 years old, they will have received a total of 126 antigenic compounds along with high amounts of aluminum (Al) adjuvants through routine vaccinations. According to the US Food and Drug Administration, safety assessments for vaccines have often not included appropriate toxicity studies because vaccines have not been viewed as inherently toxic. Taken together, these observations raise plausible concerns about the overall safety of current childhood vaccination programs. When assessing adjuvant toxicity in children, several key points ought to be considered: (i) infants and children should not be viewed as “small adults” with regard to toxicological risk as their unique physiology makes them much more vulnerable to toxic insults; (ii) in adult humans Al vaccine adjuvants have been linked to a variety of serious autoimmune and inflammatory conditions (i.e., “ASIA”), yet children are regularly exposed to much higher amounts of Al from vaccines than adults; (iii) it is often assumed that peripheral immune responses do not affect brain function. However, it is now clearly established that there is a bidirectional neuro-immune cross-talk that plays crucial roles in immunoregulation as well as brain function. In turn, perturbations of the neuro-immune axis have been demonstrated in many autoimmune diseases encompassed in “ASIA” and are thought to be driven by a hyperactive immune response; and (iv) the same components of the neuro-immune axis that play key roles in brain development and immune function are heavily targeted by Al adjuvants. In summary, research evidence shows that increasing concerns about current vaccination practices may indeed be warranted. Because children may be most at risk of vaccine-induced complications, a rigorous evaluation of the vaccine-related adverse health impacts in the pediatric population is urgently needed.
N Agmon-Levin – 1, GRV Hughes – 2, Y Shoenfeld1 – 3
1 – The Zabludowicz Center for Autoimmune Diseases, Sheba Medical Center, Tel-Hashomer, Israel
2 – Head, Lupus Research Unit, The Rayne Institute, St. Thomas’ Hospital, London, UK
3 – Sackler Faculty of Medicine, Incumbent of the Laura Schwarz-KipChair for Research of Autoimmune Diseases, Tel-Aviv University, Israel
Corresponding Author: Yehuda Shoenfeld, MD, FRCP, Zabludowicz Center for Autoimmune Diseases, Chaim Sheba Medical Center, Tel-Hashomer 52621, Israel. Email: shoenfel@post.tau.ac.il
Another cornerstone of ASIA is the complex interaction between autoimmunity and adjuvanted vaccines. On the one hand vaccines are beneficial for the vast majority of subjects including those who suffer from autoimmune-rheumatic diseases as delineated in this issue by van Assen and Bijl.16 On the other hand in a small minority of individuals vaccine can trigger the appearance of autoantibodies as documented by Vista et al.17 and Perdan-Pirkmajer et al.18 Moreover, a link between immunization and defined autoimmune diseases has been reported elsewhere and herein.2 A plausible association between the flu vaccine and polymyalgia rheumatica is reported here by Soriano et al.19 from Italy, and Soldevilla et al.20 describe three patients diagnosed with SLE following immunization with the human papilloma vaccine from the Philippines. In addition, in a retrospective analysis Zafrir et al.21 details common denominators among 93 American patients diagnosed with immune-mediated conditions following inoculation with hepatitis B vaccine. In this cohort although different autoimmune diseases were diagnosed, many manifestation were common to all patients and 86% of them fulfilled the criteria for ASIA. Of note, these cohorts signify only one side of the ASIA spectrum as they cope with distinct immune-mediated diseases while ASIA also comprises enigmatic and non-defined medical conditions. Two such conditions, the macrophagic myofasciitic syndrome and the Gulf War syndrome, are thus reviewed in this special issue by Gherardi and Authier22 and Israeli.23
Authors affiliations
University of British Columbia, Vancouver, British Columbia, Canada
Abstract
Thus far, most of the research on both neurodevelopmental and neurodegenerative disorders has been focused on finding the presumed underlying genetic causes, while much less emphasis has been put on potential environmental factors. While some forms of autism are clearly genetic, the fact remains that heritability factors cannot adequately explain all reported cases nor their drastic increase over the last few decades. In particular, studies on twins have now shown that common environmental factors account for 55% of their risk for developing autism while genetic susceptibility explains only 37% of cases. Because the prenatal environment and early postnatal environment are shared between twins and because overt symptoms of autism emerge around the end of the first year of life, it is likely that at least some of the environmental factors contributing to the risk of autism exert their deleterious neurodevelopmental effect during this early period of life. Indeed, evidence has now emerged showing that autism may in part result from early-life immune insults induced by environmental xenobiotics. One of the most common xenobiotic with immuno-stimulating as well as neurotoxic properties to which infants under two years of age are routinely exposed worldwide is the aluminum (Al) vaccine adjuvant. In this review we discuss the mechanisms by which Al can induce adverse neurological and immunological effects and how these may provide important clues of Al’s putative role in autism. Because of the tight connection between the development of the immune and the central nervous system, the possibility that immune-overstimulation in early infancy via vaccinations may play a role in neurobehavioural disorders needs to be carefully considered.
Conclusion
There is now sufficient evidence from both human and animal studies showing that cumulative exposure to aluminium adjuvants is not as benign as previously assumed. Given that vaccines are the only medical intervention that we attempt to deliver to every living human on earth and that by far the largest target population for vaccination are healthy children, a better appreciation and understanding of vaccine adjuvant risks appears warranted.
US National Library of Medicine
National Institutes of Health – Feb 2008
Wu X1, Liang H, O’Hara KA, Yalowich JC, Hasinoff BB.
Author information
Faculty of Pharmacy, University of Manitoba, 50 Sifton Road, Winnipeg, Manitoba, R3T 2N2, Canada.
Abstract
Thimerosal is an organic mercury compound that is widely used as a preservative in vaccines and other solution formulations. The use of thimerosal has caused concern about its ability to cause neurological abnormalities due to mercury accumulation during a normal schedule of childhood vaccinations. While the chemistry and the biological effects of methylmercury have been well-studied, those of thimerosal have not. Thimerosal reacted rapidly with cysteine, GSH, human serum albumin, and single-stranded DNA to form ethylmercury adducts that were detectable by mass spectrometry. These results indicated that thimerosal would be quickly metabolized in vivo because of its reactions with protein and nonprotein thiols. Thimerosal also potently inhibited the decatenation activity of DNA topoisomerase II alpha, likely through reaction with critical free cysteine thiol groups. Thimerosal, however, did not act as a topoisomerase II poison and the lack of cross-resistance with a K562 cell line with a decreased level of topoisomerase II alpha (K/VP.5 cells) suggested that inhibition of topoisomerase II alpha was not a significant mechanism for the inhibition of cell growth. Depletion of intracellular GSH with buthionine sulfoximine treatment greatly increased the K562 cell growth inhibitory effects of thimerosal, which showed that intracellular glutathione had a major role in protecting cells from thimerosal. Pretreatment of thimerosal with glutathione did not, however, change its K562 cell growth inhibitory effects, a result consistent with the rapid exchange of the ethylmercury adduct among various thiol-containing cellular reactants. Thimerosal-induced single and double strand breaks in K562 cells were consistent with a rapid induction of apoptosis. In conclusion, these studies have elucidated some of the chemistry and biological activities of the interaction of thimerosal with topoisomerase II alpha and protein and nonprotein thiols and with DNA.
VAXXED TV – My daughter is unvaccinated and very healthy
Vaccines injured my son
Our doctor fired us
My grandson has autism from vaccines
My children are injured by vaccines
College vaccinations destroyed everything I was going to do
Just saying Hi!
Vaccines killed my grandson
Linda Tells about her children and difficulties dealing with medical professionals Linda speaks about her children’s reactions to vaccinations, the troubles with school officials and medical professionals.
Mother speaks about her daughter’s reaction to MR Mother speaks at great length about her daughter’s progress through life as she develops illnesses as a result of 2 vaccine shots given at school
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.
1 Who hath believed our report? and to whom is the arm of the Lord revealed?
2 For he shall grow up before him as a tender plant,and as a root out of a dry ground:he hath no form nor comeliness;and when we shall see him,there is no beauty that we should desire him.
3 He is despised and rejected of men;a man of sorrows, and acquainted with grief:and we hid as it were our faces from him;he was despised, and we esteemed him not.
4 Surely he hath borne our griefs,and carried our sorrows:yet we did esteem him stricken,smitten of God, and afflicted.
5 But he was wounded for our transgressions,he was bruised for our iniquities:the chastisement of our peace was upon him;and with his stripes we are healed.
6 All we like sheep have gone astray;we have turned every one to his own way;and the Lord hath laid on him the iniquity of us all.
7 He was oppressed, and he was afflicted,yet he opened not his mouth:he is brought as a lamb to the slaughter,and as a sheep before her shearers is dumb,so he openeth not his mouth.
8 He was taken from prison and from judgment:and who shall declare his generation? for he was cut off out of the land of the living:for the transgression of my people was he stricken.
9 And he made his grave with the wicked,and with the rich in his death;because he had done no violence,neither was any deceit in his mouth.
10 Yet it pleased the Lord to bruise him;he hath put him to grief:when thou shalt make his soul an offering for sin,he shall see his seed, he shall prolong his days,and the pleasure of the Lord shall prosper in his hand.
11 He shall see of the travail of his soul, and shall be satisfied:by his knowledge shall my righteous servant justify many;for he shall bear their iniquities.
12 Therefore will I divide him a portion with the great,and he shall divide the spoil with the strong;because he hath poured out his soul unto death:and he was numbered with the transgressors;and he bare the sin of many,and made intercession for the transgressors.
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.
Mainstream news reporting that #BigPharma is paying everyone off! Who would have guessed? ….and this is JUST the tip of the iceberg! BEGINNING TOMORROW – AUGUST 17th – The TRUTH About Vaccines goes LIVE! Sign up here right now and share this life-changing, 7-day event with those you LOVE – Launches this Thursday, August 17th >>>>> tinyurl.com/VaccinationEducation<<<<< #TheTruthAboutVaccines #TTAV #RevolutionForChoice #VAXXED #InformedConsent
#Vaxxed #VaxxedNurses #YouMakeMeBrave #MedicalProfessionals Ruth StLeger Hoffman has 40 years of pediatric nursing experience. Her perspective provides a unique and powerful view from the other end of the needle. As a career pediatric nurse, Ruth bravely confronts the harm inflicted by vaccines through the lens of a healthcare provider having personally administered hundreds of vaccines.
#VaxxedNation #VaxxedNationTour #VaxWithMe #Nurses #40Years #PediatricNurse
Editor: Robin Aris
OpEd: Vaccines And Censorship Alive And Well In Australia
by Tom Petrie, C.D.N.
Yup, censorship and extremely narrow-minded thinking is alive and well in Australia! Those old enough will remember Dr. Archie Kalakeranis who, in the late 1960’s and throughout the 1970’s, linked SIDS to extreme vitamin C deficiency, also known as scurvy. The grief he took for over 15 years is not unlike the grief that has fallen upon Dr. Andrew Wakefield today in Britain! If one were to read his 1998 Lancet paper carefully, they would note that he only suggested “further investigation of the M.M.R. is necessary” (w/regard to GI troubles in children). In other words, he wasn’t an “anti-vaxxer,” but just someone who was doing what any good clinician would (and should) do: Investigate and report on what they see, not just what they’re “suppose to see.”
Yet, if someone wants an honest investigation of vaccines and their link to this or that health challenge, they, (like some ardent vaccine advocates in Australia claim), suddenly become “anti-vaxxer’s!” This is really ridiculous and it’s like me becoming “anti-running,” because I might sprain my ankle while running or being anti-Frisbee, because it might hurt if it hits me!
As explained in Anne Dachel’s book, “The BIG Autism Cover-up,” the media has been covering up the environmental causes of this epidemic for decades now in the United States. This censorship also clearly exists in Australia as illustrated by sad efforts to censor the filming of VAXXED in various towns there.
Censorship can be active or passive. It is active as is happening now in Australia in efforts to STOP the showing of VAXXED, which has had record screenings in a number of locations. In other cases, the censorship is more passive (as proven by Dr. K’s experiences four decades earlier): A clear indication that vaccines can precipitate SIDS was simply ignored entirely by the medical profession and this censorship and cover-up has continued to this day, year 2017.
So ask yourself if you knew that SIDS is primarily “infantile scurvy” often precipitated by a mere vaccine &/or a “mild cold”?! So if public health officials can ignore that a “mere vitamin deficiency” can precipitate a death of an infant, is it NOT much of a stretch to say they could routinely ignore that vaccines can cause various health challenges in children? Not at all!
If you have children, you may want to read this…
The health and safety of our children are of utmost importance → http://bit.ly/2hEO60r
We should all be informed about both the benefits and the risks associated with vaccines — without pressure, propaganda, or agenda.
That’s why we have brought together more than 60 of the world’s foremost health experts to investigate both sides of this contentious debate to give you the science, the history, and the untold story… the REAL information you need to make an informed decision on how to best protect your child.
The Truth About Vaccines is a 7-episode documentary series that you can watch for FREE. Click here to watch the trailer → http://bit.ly/2hEO60r
15 Things You Don’t Know About Polio
1. A pesticide common in the 1800’s was called Paris Green. A green liquid because it was a combination of copper and arsenic or lead and arsenic. Some of the most toxic substances known to humankind. This super toxin was also used as a dye, in many items, including wall paper and paint. It was the sole focus of murder mystery novels at the time, as arsenic was known to be a very efficient way to stage a murder “for unknown reasons”, as arsenic kills but is hard to detect after the victim succumbs to the poison. http://bit.ly/2urZvqu and http://bit.ly/2wL5tPT
2. This pesticide worked by causing neurological damage in the bugs, causing organ failure.
3. Polio consists of symptoms synonymous with neurological damage, causing organ failure.
4. Heavy metal poisoning from lead, mercury and other similar heavy metals manifest lesions on neurological tissues, meaning the toxin destroys the nerve/communication pathways connecting the brain to the organs in the body. http://bit.ly/1OLcFgG
5. Polio victims present lesions on neurological tissue, that cause the organs to malfunction all around the body. (lungs, heart, nerves that control walking etc)
6. Polio outbreaks hit throughout the summer, only during pesticide spraying times. (not the sunless and damp winter/spring seasons regarding other disease outbreaks)
Vaccine damage is not rare…These catastrophic injuries and tragic deaths are not “anecdotal”…The science is not settled…and we’re not going away. Join us – Help us spread this crucial awareness – Share this life-changing, 7-day event with those you LOVE – Launches this Thursday, August 17th:
>>>>> tinyurl.com/TTAVisBack <<<<<
#TheTRUTHaboutVaccines #RevolutionForChoice #Vaxxed #HearThisWell #NotGoingAway
(News-clip from 2011)
Toddler who was given an adult flu shot is left severely brain damaged and unable to walk or talk
JANE HANSEN, The Sunday Telegraph
A TODDLER taken to the doctor for a child’s flu shot was left unable to walk or talk after being given a version of the drug banned for under fives.
Lachlan Neylan suffered severe brain damage, including seizures and swelling of the brain, known as encephalopathy, after a GP accidentally administered the CSL Fluvax shot in March last year.
His parents Stacey and Adrian Neylan said Lachlan’s temperature soared and he began having fits within seven hours of receiving the injection.
“He just collapsed and started to have seizures,” Mr Neylan said. “Doctors said they thought our son wouldn’t make it through the weekend. It was terrifying.”
Mr Neylan said before the injection their son had been a “walking, talking toddler”, but after the injection “he was back to being a three month old; he couldn’t sit, walk, or use his arms”.
While other flu vaccines are approved for children, Lachlan, was given the contraindicated Fluvax, which was banned for children under five in 2010 after mass injections triggered febrile convulsions in one in every 100 children; 10 times the expected rate.
The family said they were concerned doctors were still using Fluvax on children, despite the ban. A spokesperson for the Department of Health said there had been “43 confirmed notifications of CSL Fluvax being administered to children under five years of age in Australia” this year. The GP in question has admitted error and the government’s adverse events report also admits the error.
“This was a mistake, and the doctor has admitted it, but it is still happening and we don’t want anyone else to go through what we have been through,” Mr Neylan said.
Nicolai Levashov
About Spirit, Mind and many other things…
Here I would like to tell you about myself. In order to do this I give some official documents (I call them “Credentials”) and my autobiographic chronicle where I describe some events of my life and offer my interpretation of my views on life in general and some phenomena in particular.
11 year-old Bolivian girl in a coma with a diagnosis of Guillian Barre Symdrome. Mother says the symptoms began the same day as her injection of HPV vaccine. Doctors state that it’s a coincidence. Menor con Guillain Barre está en coma; malestar inició por dosis contra VPH dice la madre
14/05/2017-08:33
Menor con Guillain Barre está en coma
Afirman que malestar inició por dosis contra VPH
Una escolar de 11 años está internada en terapia intensiva en el hospital de niños Mario Ortiz. Según la madre, los médicos afirmaron que se trata de Guillain Barre, una enfermedad que afecta al sistema nervioso y que provoca parálisis. Aunque la mamá de la menor aseguró que los síntomas iniciaron el mismo día en que su hija fue vacunada contra el Virus del Papiloma Humano (VPH), que tiene como objetivo prevenir cáncer cérvico.
Desarrollo del caso. La madre de la menor, Rosy Mary García, explicó que sospecha que el estado de su hija es producto de la vacuna contra el VPH pues un día después de que se le aplicó la dosis, el 26 de abril, presentó malestares, primero náuseas y fiebre y luego de algunos días dolor en la garganta. Aseguró que la llevó a internar al hospital Francés, donde sospechaban de rabia, después de varios estudios no se confirmó. Agregó que este lunes la tuvieron que trasladar al hospital de niños, directamente a terapia intensiva. “Todo comenzó con la vacuna”, insistió la mamá a tiempo de indicar que tiene otra hija, pero como tiene solo 9 años, no le aplicaron la dosis.
Aseguró que las compañeras de su hija mayor, que estudian en la unidad educativa Amsterdam en la zona de Los Lotes, igual presentaron malestares, el mismo 26, aunque solo fue mareos y vómitos.
Congratulations Chelsea Clinton! Del crowned you the #Vaxhole of the week! Tune in every Thursday at 11 am pst for a new vaxhole. @HighWireTalk @DelBigtree #Vaccineswork?
Dr. Brennan. Theresa Deisher, molecular biologist – human dna in vaccines and autism. #VaXism NEWS
Snoop Dogg Exposes Vaccines
If You Vaccinate, Ask 8 Questions – http://ow.ly/4KyZ30eqxeG
Vaccines are pharmaceutical products that come with risks that can be greater for some people. No vaccine is safe for everyone.
If you choose to vaccinate, ask 8 questions before you do:
Number One: Am I sick right now? Getting vaccinated while sick could increase risks for a vaccine reaction or lower vaccine effectiveness.
Number Two: Have I had a bad reaction to a vaccination before? Getting re-vaccinated after a previous vaccine reaction could cause a more serious reaction, injury or death.
Number Three: Do I have a personal or family history of vaccine reactions, neurological disorders, severe allergies or immune system problems? Always review your personal and family medical history when evaluating vaccine benefits and risks.
Number Four: Do I know the disease and vaccine risks? Learn about disease and vaccine risks that could be greater for you or your child.
Number Five: Do I have full information about the vaccine’s side effects? Before you take a risk, find out what it is for each vaccine you or your child will receive.
Number Six: Do I know how to identify and report a vaccine reaction? Learn how to recognize vaccine reaction symptoms and where and how to report them.
Number Seven: Do I know I need to keep a written record, including the vaccine manufacturer’s name and lot number, for vaccinations? The National Childhood Vaccine Injury Act of 1986 requires all vaccine providers to record information about vaccines given to you or your child.
Number Eight: Do I know I have the right to make an informed choice? Informed consent to medical risk taking, including vaccine risk taking, is a human right.
Explore NVIC’s Ask 8 Information Kiosk for referenced information and a variety of materials designed to educate you about vaccines, diseases and how to make educated vaccine decisions. You can download posters and brochures to share with others or send an ecard to family and friends. You can also post or read personal vaccination experiences on this website. Click here to learn more and start your journey! http://ow.ly/4gee30eqxQh
Friends please watch and SHARE this short clip entitled “The Fateful Decision Of Vaccinations“, and then join us for 7-part “The Truth About Vaccines” docuseries starting August 17!
To make sure you secure your spot to watch for FREE, register here right now: http://bit.ly/TTAVTrailerttavfb
Joshua Coleman interviews Dr. Andrew Wakefield and asks what would happen if they withdrew the MMR vaccine now that the vaccine has made babies immunocompromised from measles. #WeAreJoshuaColeman #Vaxxed
YOUTUBE: https://youtu.be/bfkXHGkdHc4
Vaccination Policy and the U.K. Government: The Untold Truth
What do Munchausen Syndrome by Proxy, Gulf War Syndrome and shady vaccination policies have to do with the UK government? By using a wide selection of studies, papers and documents released under the Freedom of Information Act, we uncover how, by prioritizing vaccination policy over vaccine safety, the Joint Committee of Vaccination and Immunization (JCVI), the Department of Health (DH), the Committee on Safety of Medicines (CSM) and the Ministry of Defence may have damaged the health of millions of people worldwide.
Vaccine Revolt 1904 (Portuguese: Revolta da Vacina)
To eradicate smallpox, Cruz convinced the Congress to approve the Mandatory Vaccination Law (October 31, 1904), which permitted sanitary brigade workers, accompanied by police, to enter homes to apply the vaccine by force.
The population was confused and discontented. The city seemed in ruins, many people had lost their homes, while others had had their homes invaded by the health workers and police. Articles in the press criticized the action of the government and spoke of possible risks of the vaccine. Moreover, it was rumored that the vaccine would have to be applied to the “intimate parts” of the body (or at least that women would have to undress in order to be vaccinated), aggravating the anger of the population, and resulting in a popular rebellion.
The approval of the Vaccination Law was the proximate cause of the revolt: on November 5, the opposition created the Liga Contra a Vacina Obrigatória (League Against Mandatory Vaccination).
From November 10 through 16, the city became a battlefield. The excited population looted shops, overturned and burned trams, made barricades, pulled out tracks, broke poles, and attacked government forces with rocks, sticks, and debris. On November 14, the cadets of the Escola Militar da Praia Vermelha (military college) also mutinied against the government’s actions. In reaction, the government suspended mandatory vaccination and declared a state of siege. The rebellion was contained, leaving 30 dead and 110 wounded. Hundreds of imprisoned people were deported to the then frontier region of Acre.
This is just a tiny snapshot of the pain and suffering occurring WORLDWIDE right after the Gardasil injection. We do not need more “studies” and more mindless meetings to use our COMMON SENSE and see that this mass-poisoning of our children must be put to an end! Right now, there is a 9-part docu-series available to everyone who intends to protect their families from the heartless industry profiting from these tragedies >>> tinyurl.com/9Episodes
✴️ 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 #Gardasil #Cervarix #Seizures
100% Proof! Human DNA in Vaccines
Presentation recorded on February 16, 2017 in Sonora, California with Marcella Piper-Terry. #Vaxxed #PrayBig #RecombinantDNA #InsertionalMutagenesis #FetalCellLine #ProLife #Abortion #ChooseLife #RespectLife #MarchForLife #MRC5 #WI38 #RA273 #WALVAX2
Youtube Link: https://youtu.be/dlqFQLLOTEU
Editor: Robin Aris
Finding Hope after a Gardasil Disaster
September 19, 2013
By Tracie Toler Moorman, Overland Park, Kansas
Gardasil: An uphill battle for Maddie
Gardasil: Please research before you decide!
It is difficult to know where to begin when charting the 19-month journey my daughter and family have traveled since she was injured by the Gardasil vaccine in 2012. Maddie, my girl, as I like to call her, was a 15-year old happy, healthy, straight-A, honors/AP high school student. It was easy being her mother; it was a joy to be with her. She lit up the room when she entered. She was a beautiful writer and an amazing guitar player. That was my girl.
In December of 2011, she developed a hormone imbalance. It was rather bothersome but her pediatrician did not seem too concerned. In retrospect, I wonder if this hormone imbalance may have pre-selected her for injury from the vaccine. Perhaps it was genetics. I may never know. Her pediatrician suggested birth control pills to regulate the hormones and I took her to my gynecologist for a second opinion. My doctor concurred. Birth control pills were prescribed and while we were in the office, the gynecologist recommended the vaccine. Her pediatrician had also been recommending it. I trusted both doctors and believed them when they said that Gardasil was safe and the threat of cervical cancer was real.
As her mother, I wanted to protect her from any form of harm so I thought it made sense to begin the three-part vaccine. Maddie had always been tough when receiving vaccines but this one was very different. She described it as similar to being hit in the arm with a baseball bat swung by a professional ball player. It was excruciating pain.
Looking back, Maddie got sick after the first dose of the vaccine, but it was masked by symptoms we attributed to the birth control pills. After five days of headaches and nausea, I called the gynecologist and reported that she was not well. The doctor switched her from one birth control pill to another. The nausea subsided a bit but the headache lingered. She was still able to go about her normal routine most days.
UFC Veteran Speaks Out Against Vaccines After Tragic Death of Son
Posted on July 1, 2017
By Brandon Turbeville
“This is unacceptable, I will fight for my son, this happened to the wrong family.” – Nick Catone
Former UFC fighter, Nick Catone, is making waves on social media. But while many fighters are drawing attention to themselves for attacking their opponents, Catone is gathering attention for another reason: his vocal criticism of vaccination.
For him, the issue is very personal since on May 12, his otherwise healthy 20-month-old son passed away in the middle of the night. While the family was initially perplexed as to how a healthy little boy could just simply die without warning, consultations with numerous doctors and even an autopsy yielded no results. Instead, the cause of Nicholas’ death was listed as “natural.”
Shortly after, however, Catone began hearing stories from other parents regarding their child’s adverse reactions to vaccines, ranging from seizures to autism and death. Catone began doing his own research and is now convinced that it was the vaccine that killed his son.
Italian Government To Remove Unvaccinated Children From Parents
June 17, 2017 Baxter Dmitry
Major demonstrations have rocked Italy this past week as the government attempts to pass a new law that will triple the number of mandatory vaccinations for Italian children and threatens to remove unvaccinated children from their parents.
“Lorenzin cancel your law, we are not your herd,” tens of thousands of Italians chanted at a protest in Rome, holding banners decrying government overreach into their homes and the health of their children.
Under the draconian new law, Italian children who have not received the full schedule of 12 mandatory vaccinations will lose their right to attend school, the parents will be fined up to 7,500 euros ($8396), and in case the Italian government had not already made it clear they are completely in the pockets of Big Pharma, they also announced that unvaccinated children will be taken away by local child protective services.
But Italians of all stripes are rising up in defiance of the new law. Politicians, associations, doctors, lawyers, and parents came together for the first time on the streets of Rome to make their voices heard.
One protestor shared a heart-rending account of his difficulties raising a vaccine damaged child in Italy:
“I am here as a parent, as a parent of a child who, unfortunately, has been damaged by a hexavalent vaccine. I am a parent who has tried to follow the path of the law and I have found myself in front of shameful situations, when the state courts consider vaccine injured kids as, allow me to say, the town’s idiots, the losers.”
15,000 PEOPLE MARCH IN ROME AGAINST AN OPPRESSIVE NEW MANDATORY VACCINE LAW
from Francesca Alesse
Vaccines, Retroviruses, DNA, and the Discovery That Destroyed Judy Mikovits’ Career
December 1, 2015 by Allene Edwards
Last updated on: March 15, 2017
Judy Mikovits, PhD is a biochemist and molecular biologist with more than 33 years of experience. Internationally known, a veritable “rock star” of the scientific world, she served as the director of the lab of Antiviral Drug Mechanisms at the National Cancer Institute before directing the Cancer Biology program at EpiGenX Pharmaceuticals. She later developed the first neuroimmune institute. Her early work focused on cancer and HIV, her latest on Chronic Fatigue Syndrome and autism. She has published more than 50 peer-reviewed articles.
In 2011, she made the discovery that destroyed her career. She found that at least 30% of our vaccines are contaminated with gammaretroviruses. Not only is this contamination associated with autism and chronic fatigue syndrome, it is also associated with Parkinson’s, Lou Gehrig’s disease, and Alzheimer’s.
When she released this shocking information, she was warned by Dr. Andrew Wakefield that she would become a target, just as he had been. But she assured him that all of her work had been properly reviewed and, of course, she was safe.
She was wrong. She was threatened and told to destroy her data; she refused. She was fired, then arrested for supposedly stealing her data from her worksite. She had been facing charges and was bound by a gag order from the court for the last four years. Recently, charges were dropped and the gag order was lifted. Dr. Mikovits is now free to talk, and boy is she talking.
The retroviruses contaminating vaccines originate from mice used for research. Dr. Mikovits asks, “How many new retroviruses have we created through all the mouse research, the vaccine research, gene therapy research? More importantly, how many new diseases have we created?”
“When they destroyed all of our work, and discredited everything I or Frank Ruscetti had ever published, and arranged for the publication of my mug shot in Science, the NIH very deliberately sent the message to researchers everywhere about what would happen to any honest scientist who dared ask those important questions.”
New technology now exists to clean up retroviruses in vaccines and blood. Dr. Mikovits believes we will win this war, that we will eventually clean up vaccines, stop vaccinating infants, and stop injecting our children with multiple vaccines. But she also believes the government will continue to cover up their culpability in the current epidemic of autism and other diseases.
Mercury and Aluminum in Vaccines: a Primer on NVIC’s Vaccine Ingredients Calculator
Posted on January 30, 2012 by Marcella
by Marcella Piper-Terry, M.S.
This article will tell you how to recognize the symptoms of aluminum toxicity. Aluminum toxicity is something I am very concerned about. In 2004, a large portion of the mercury that was previously used in childhood vaccines was removed from those sold and administered in the United States.
Many people, including many physicians, believe and will tell you “There is no mercury in vaccines anymore. They took that out years ago!” This is not true. For a list of vaccines that still contain mercury above EPA safety levels click here. Seven vaccines are reported to still contain thimerosal, which is 49.5% mercury.
The statement that there is no thimerosal in vaccines anymore is usually made by those attempting to make the claim that there is no link between autism and vaccines. These folks will frequently say things like, “They removed mercury from the shots and the autism rate has continued to go up! That proves vaccines don’t cause autism!”
Ummm….. No. and No.
At almost the exact same time they took a large percentage of mercury out of what was then the childhood schedule, the CDC and ACIP made a new recommendation. The vaccine-pushers recommended every pregnant woman receive a flu shot during the second trimester. In addition, the recommendation was made that every child receive annual flu vaccines, beginning at six months of age.
Flu vaccines often contain high levels of thimerosal, which is 50% mercury. Those pregnant mothers and infants who are most likely to get the flu vaccines with mercury are those who are the least likely to have adequate health care. Physicians in private practices are more likely to use single-dose vials. It’s the multi-dose vials that contain the highest level of Thimerosal: 50 mcg. for the adult dose and 25 mcg. for the pediatric dose. That means when a pregnant woman gets a flu shot from her local health department, Walmart, CVS, University Health Center, etc… her tiny fetus is being injected with levels of toxic mercury that are hundreds of times above the “safe limit” (as defined by the EPA).
If the fetus survives and if he/she is vaccinated again at six months, 18 months and every year after that, and if those vaccines are administered from multi-dose vials, he or she is getting a whopping dose of mercury every year.
Study – Hepatic response to aluminum toxicity: dyslipidemia and liver diseases.
Abstract
Aluminum (Al) is a metal toxin that has been implicated in the etiology of a number of diseases including Alzheimer’s, Parkinson’s, dialysis encephalopathy, and osteomalacia. Al has been shown to exert its effects by disrupting lipid membrane fluidity, perturbing iron (Fe), magnesium, and calcium homeostasis, and causing oxidative stress. However, the exact molecular targets of aluminum’s toxicity have remained elusive. In the present review, we describe how the use of a systems biology approach in cultured hepatoblastoma cells (HepG2) allowed the identification of the molecular targets of Al toxicity. Mitochondrial metabolism is the main site of the toxicological action of Al. Fe-dependent and redox sensitive enzymes in the tricarboxylic acid (TCA) cycle and oxidative phosphorylation (OXPHOS) are dramatically decreased by Al exposure. In an effort to compensate for diminished mitochondrial function, Al-treated cells stabilize hypoxia inducible factor-1α (HIF-1α) to increase ATP production by glycolysis. Additionally, Al toxicity leads to an increase in intracellular lipid accumulation due to enhanced lipogenesis and a decrease in the β-oxidation of fatty acids. Central to these effects is the alteration of α-ketoglutarate (KG) homeostasis. In Al-exposed cells, KG is preferentially used to quench ROS leading to succinate accumulation and HIF-1α stabilization. Moreover, the channeling of KG to combat oxidative stress leads to a reduction of l-carnitine biosynthesis and a concomitant decrease in fatty acid oxidation. The fluidity and interaction of these metabolic modules and the implications of these findings in liver-related disorders are discussed herein.
Study – Mechanisms of aluminum adjuvant toxicity and autoimmunity in pediatric populations
L Tomljenovic, CA Shaw
First Published January 10, 2012
Abstract
Immune challenges during early development, including those vaccine-induced, can lead to permanent detrimental alterations of the brain and immune function. Experimental evidence also shows that simultaneous administration of as little as two to three immune adjuvants can overcome genetic resistance to autoimmunity. In some developed countries, by the time children are 4 to 6 years old, they will have received a total of 126 antigenic compounds along with high amounts of aluminum (Al) adjuvants through routine vaccinations. According to the US Food and Drug Administration, safety assessments for vaccines have often not included appropriate toxicity studies because vaccines have not been viewed as inherently toxic. Taken together, these observations raise plausible concerns about the overall safety of current childhood vaccination programs. When assessing adjuvant toxicity in children, several key points ought to be considered: (i) infants and children should not be viewed as “small adults” with regard to toxicological risk as their unique physiology makes them much more vulnerable to toxic insults; (ii) in adult humans Al vaccine adjuvants have been linked to a variety of serious autoimmune and inflammatory conditions (i.e., “ASIA”), yet children are regularly exposed to much higher amounts of Al from vaccines than adults; (iii) it is often assumed that peripheral immune responses do not affect brain function. However, it is now clearly established that there is a bidirectional neuro-immune cross-talk that plays crucial roles in immunoregulation as well as brain function. In turn, perturbations of the neuro-immune axis have been demonstrated in many autoimmune diseases encompassed in “ASIA” and are thought to be driven by a hyperactive immune response; and (iv) the same components of the neuro-immune axis that play key roles in brain development and immune function are heavily targeted by Al adjuvants. In summary, research evidence shows that increasing concerns about current vaccination practices may indeed be warranted. Because children may be most at risk of vaccine-induced complications, a rigorous evaluation of the vaccine-related adverse health impacts in the pediatric population is urgently needed.
Study – Aluminum Adjuvant in Vaccines Causes Risk to Children According to New Journal Report
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A new Canadian study of the mechanisms of aluminum adjuvant toxicity in pediatric patients confirms that immune challenges during early development, including those vaccine-induced, can lead to permanent detrimental alterations of the brain and immune system function. Lucija Tomljenovic, PhD and Christopher A. Shaw, PhD of the University of British Columbia’s evidence-based study was recently published in Lupus, the only fully peer reviewed international journal devoted exclusively to lupus (and related disease) research.
Summary
Immune challenges during early development, including those vaccine-induced, can lead to permanent detrimental alterations of the brain and immune system function. Experimental evidence also shows that simultaneous administration of as little as two to three immune adjuvants can overcome genetic resistance to autoimmunity. In some developed countries, by the time children are 4 to 6 years old, they will have received a total of 126 antigenic compounds along with high amounts of aluminum (Al) adjuvants through routine vaccinations. According to the US Food and Drug Administration, safety assessments for vaccines have often not included appropriate toxicity studies because vaccines have not been viewed as inherently toxic. Taken together, these observations raise plausible concerns about the overall safety of current childhood vaccination programs.
When assessing adjuvant toxicity in children, several key points ought to be considered:
1) During prenatal and early postnatal development the brain is extremely vulnerable to neurotoxic insults;
2) Aluminum is a neurotoxin and a strong immune stimulant. Hence, aluminum has all the necessary biochemical properties to induce neuro-immune diseases. Autism is one such disease. Namely, autism is characterized by dysfunctional immunity and abnormalities in brain function;
3) In adult humans aluminum vaccine adjuvants have been linked to a variety of serious autoimmune and inflammatory conditions, yet children are regularly exposed to much higher amounts of aluminium from vaccines than adults;
4) It is often incorrectly assumed that peripheral immune challenges (analogous to vaccinations) do not affect brain function. However, it is now clearly established that there is a cross-talk between the nervous and the immune system. It is also demonstrated that this cross-talk plays a crucial role in both immunoregulation as well as brain function. In turn, perturbations of the neuro-immune regulatory system have been demonstrated in many autoimmune diseases and are thought to be driven by a hyperactive immune response;
5) The same components of the neuro-immune regulatory system that have key roles in both brain development and immune function are heavily affected by aluminum adjuvants;
In summary, research evidence shows that increasing concerns about current vaccination practices may indeed be warranted. Because children may be most at risk of vaccine-induced complications, a rigorous evaluation of the vaccine-related adverse health impacts in the pediatric population is urgently needed.
Tetanus Vaccine Causes a New Disease Known as Antiphospholipid Syndrome
July 3, 2017
by Heidi Stevenson
Gaia-Health.com
The vaccine junta is not only unconcerned with vaccine-induced diseases, it’s massively gearing up this vaccine arms race against the human race. It’s known that tetanus vaccine causes a new disease, antiphospholipid syndrome. New adjuvants are composed of phospholipids, a potential disaster.
The tetanus vaccine causes a new disease known both as Hughes syndrome and antiphospholipid syndrome (APS). It’s an autoimmune condition that can attack any part of the body, though is best noted for heart attacks and killing fetuses. It’s likely that APS will become more common with the new generation of vaccine adjuvants now being produced.
The sufferers of (APS) are mostly women, and its diagnosis is often made as a result of multiple pregnancy losses. As is typical of new diseases, research is focused on finding a genetic cause, in spite of the fact that the connection with vaccines is well known and documented.
As the name implies, APS is a condition in which phospholipids, natural and necessary substances required by every part of the body, is seen as an infectious agent by the immune system. So, this substance that exists in every cell becomes subject to attack. Symptoms include:
Blindness
Cardiovascular:
Deep vein thrombosis (clots in veins)
Phlebitis
Thrombocytopenia (deficiency of blood platelets, causing bleeding & bruising)
Atherosclerosis
Pulmonary embolus (clots in the lungs)
Heart valve abnormatilies
Stroke
Headaches & migraines
Miscarriages
Neurological disorders:
Epilepsy
Chorea (sudden uncontrollable jittery movements)
Transverse myelitis (inflammation of the spinal cord)
Multiple sclerosis
Cognitive dysfunction
Skin disorders, including mottling, ulcers, and necrosis
APS can also be diagnosed—more accurately, misdiagnosed—as lupus erythematosus, which is another vaccine-induced condition.
APS and Vaccines
One study calls Hughes syndrome the “classical antiphospholipid syndrome”[1]. That study refers to similarities between plasma protein beta-2-glycoprotein-I (β2GPI), which is attacked in APS, and the tetanus vaccine. That is, the tetanus antigen has parts that are virtually identical to β2GPI, which is found virtually everywhere in the body.
Another study documents how APS can be induced in laboratory animals with tetanus vaccination[2]. Many large number of other studies document and investigate the connection between vaccines and antiphospholipid syndrome[3,4,5,6,7,8].
These studies leave little doubt that APS is caused by vaccines. That should come as little surprise, since it was first identified as a disease during the 1980s. If this disease existed prior to vaccines, it was so rare that it was unknown. Now, it can take its place among a growing list of vaccine-induced conditions, including rheumatoid arthritis, macrophagic myofasciitis, multiple sclerosis, autism, and siliconosis. The list keeps growing and many believe that all these conditions should be included under a single name, autoimmune/inflammatory syndrome induced by adjuvants, or ASIA.
Dara Berger, author of “How to Prevent Autism: Expert Advice from Medical Professionals,” DEMOLISHES pro-vax propaganda. You too can be JUST as informed and confident in your decisions ~ Learn everything you need to know, for FREE while this ground-breaking docu-series is still available! ➤➤➤ tinyurl.com/9Episodes
✴️ 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 #Measles #WarriorMom #VaccineInjury #Autism
The vitamin with a black box warning
Interview recorded on February 5, 2017 in Riverside, California.
Editing: Robin Aris
“Just a Vitamin” – Child with MTHFR Poisoned by Vitamin K Shot at Birth
Nicole was firm in her decision to delay all vaccines, but she was under the common misconception that the Vitamin K shot was, “just a vitamin”. She believes that her now 13 year-old son, Wyatt, was poisoned by the “Vitamin” K shot at birth. The shot now carries a black box warning.
Interview recorded on February 2, 2017 in San Diego, California #Vaxxed #VaxxedNation
Editor: Robin Aris
I said please give him everything
Interview recorded on February 5, 2017 in Riverside, California.
Editing: Robin Aris
VaxXed Stories: Lily in Florida
Lily was born with Moebius Syndrome, believed to have been caused by her mothers flu vaccine while pregnant. Lily suffered subsequent damage from her childhood vaccines as well.
Expert believes the lower teen birth rate may be due to infertility from Gardasil
By Erin Elizabeth – June 23, 2017
Based on birth certificate data, teen birthrates are dropping. In 2015, the teen birthrate hit a record low, dropping 8%. In 2014, the birthrate per 1000 teen girls (aged 15 to 19) fell to 22.3 births. Since 1991 there’s been a 64% decrease.
The CDC is touting (as you can imagine) the success of birth control. After all, they’ve spent decades as “pharma’s marketing voice.”1 But, what if something else more sinister is responsible for the lower birthrate?
According to Norma Erickson from SaneVax, the Gardasil vaccine being given to teens to “prevent” HPV might actually be causing infertility (among other things):
“I would suspect that quite a bit of it may be related to Gardasil, particularly since there have been campaigns targeting black, Hispanic and ‘at risk’ young women (those incarcerated) – coincidentally also those with the highest teen birth rates.
I have personally spoken with a 17 year old California boy who after the second injection is impotent. He said one of his friends has the same problem, but is too embarrassed to speak of it (even to his parents).
We are barely seeing the tip of the iceberg.” 2
Gardasil: Don’t let your child become “one less”
By Erin Elizabeth – March 7, 2015
Today we have an article written by Shannon Powers
SaneVax.org
I share our story hoping our experience will save another from becoming “one less” healthy child.
Our fifteen year old daughter, Leah is vaccine injured. It all began March 30th 2011. Leah was 11 years old, soon to be 12. We had been referred to an Adolescent doctor so Leah could be placed on oral contraceptives to help prevent cysts from forming on her ovaries.
A month prior, February 20, 2011 Leah had an Oophorectomy losing her left ovary. We were told since we had just gone through this scary ordeal, in order to keep her healthy we needed to vaccinate with the Gardasil vaccine.
Trusting in doctors and believing what they recommend is best, I never questioned their belief that this was a “must” for Leah’s health. After all, Leah had received all her recommended vaccines prior to Gardasil. What could we possibly have to worry about?
First, I have to tell you Leah has a very high tolerance for pain. The only way I knew I needed to take her to the hospital in February was because she was clammy and dry heaving. The surgeon who performed the Oophorectomy came and told us after, that she should have been in excruciating pain.
She laughed when telling Leah, “I tells my kids to quit complaining all the time, but YOU need to complain and let us know when something is wrong in your body. You know your body best and when something is off let mom and dad know!”
Recovery went smooth and we then were released and referred to the adolescent doctor for all of Leah’s follow-up care.
Holistic MD Exposes Gardasil Coverup: Deceptive Emails by Health Officials
By Erin Elizabeth – January 29, 2016
Holistic MD Exposes Gardasil Coverup
By: Brian Shilhavy
“I predict that Gardasil will become the greatest medical scandal of all times because at some point in time, the evidence will add up to prove that this vaccine, technical and scientific feat that it may be, has absolutely no effect on cervical cancer and that all the very many adverse effects which destroy lives and even kill, serve no other purpose than to generate profit for the manufacturers.”
This past week, Dr. Sin Hang Lee, M.D., F.R.C.P. (C), FCAP, director of the Milford Molecular Diagnostics Laboratory in Connecticut, proved Dr. Dalbergue’s prediction correct, when he published a letter sent to the U.S. CDC, the World Health Organization, the Ministry of Health in Japan, and others, documenting “scientific misconduct” among the world’s leading health organizations tasked with providing vaccine safety, by deliberately misleading Japanese health authorities on the safety of the HPV vaccine.
Japanese health authorities had halted their recommendation of the HPV vaccines in 2013 due to safety concerns. Japanese officials began a full investigation into the HPV vaccines at that time.
Dr. Sin Hang Lee has allegedly discovered that at a public hearing on HPV vaccine safety which was held in Tokyo, Japan on February 26, 2014, members of the Global Advisory Committee on Vaccine Safety (GACVS), the World Health Organization, the CDC and other scientific/health professionals:
deliberately set out to mislead Japanese authorities regarding the safety of the human papillomavirus (HPV) vaccines, Gardasil® and Cervarix®, which were being promoted at that time.
Dr. Lee discovered the alleged deception by obtaining a series of emails via a Freedom of Information request submitted in New Zealand.
According to Dr. Lee, these emails reveal:
that Dr. Robert Pless, the chairperson of the Global Advisory Committee on Vaccine Safety (GACVS), Dr. Nabae Koji of the Ministry of Health of Japan, Dr. Melinda Wharton of the CDC, Dr. Helen Petousis-Harris of Auckland University, New Zealand, and others (including WHO officials) may have been actively involved in a scheme to deliberately mislead the Japanese Expert Inquiry on human papillomavirus (HPV) vaccine safety before, during and after the February 26, 2014 public hearing in Tokyo. (Source.)
Healthy Boy Dies After Gardasil Injection
By Erin Elizabeth – July 7, 2016
Joel Gomez was just 14 years old. Medical records show he was a healthy boy who made all his check-ups at his pediatrician’s office.
He had no pre-existing health issues.
He had no cardiac abnormalities, psychological disorders, substance abuse, or any other issues.
But, he had a vaccine the day before he died.
From the article:
“An expert hired by the family of a boy who died after his second Gardasil injection has testified that Gardasil likely caused the boy’s death. The case – Gomez versus USDOH: Petition No. 15-0160V1 – was filed by a California law firm for petitioners Adan Gomez and Raquel Ayon, on behalf of their deceased son Joel Gomez. The petition states, in part:
“Joel Gomez received a Merck Gardasil vaccine on June 19, 2013 and again on August 19, 2013, and died in his sleep the following day on August 20, 2013. The death was caused in fact by receiving the Gardasil Vaccine.
Gardasil did cause or contributed to a myocardial infarction in the decedent, and that the second dose of Gardasil finally caused a fatal hypotension in this case on the day of vaccination. There was no other plausible cause for the death of Joel Gomez. . .”
Sadly, Joel was another casualty of the Gardasil vaccine.
Natural News – Top 9 vaccines you NEVER need and exactly why the CDC has to scare everybody into getting them
Monday, June 13, 2016 by: S. D. Wells
What the medical industrial complex doesn’t want anyone to know
The real reason many children and babies have weaker immune systems than adults is because they receive over 50 toxic vaccines before age 7, as recommended by the CDC and the state department – and enforced at gunpoint in certain states, like California.
Chicken pox is a common childhood disease caused by a virus that lasts two to four days, and then most children are immune to it for life. Measles is like a cold that can include a cough, fever and a blotchy rash that fades after a few days and peels. Mumps is an acute viral infection usually accompanied by a mild fever lasting a couple of days, with a sore throat and swollen glands. What the medical industrial complex doesn’t want anyone to know is that the normal human body that’s not beaten down and infected by vaccine toxins and food toxins beats these infections easily. Same goes for the Zika virus, which does not cause deformations in babies; that’s all a huge lie and scare tactic. The swine flu was a hoax, as was the vaccine, and those vaccine manufacturers have paid out millions in damages due directly to that toxic jab. Then there’s the MMR vaccine that causes autism, as confessed by the head CDC scientist, Dr. William Thompson.
The anthrax vaccine is highly experimental and dangerous, and the polio vaccine, given by injection or through oral or nasal application, actually spreads the disease, with those children themselves becoming carriers, infecting other children and family members. It’s criminal and the vaccine industry knows it, but the profits from selling the vaccine to all the paranoid parents and brainwashed, uneducated folks through fear-mongering far outweigh the damages paid out in settlements for health detriment. It’s a simple formula for evil capitalistic success: sell millions of toxic vaccines and create a slush fund from about 1 percent of those profits to shut parents up who try to sue the industry when their kids and babies become crippled and maimed.
The only thing parents should be scared of is the vaccine industry. Take measures to build immunity with organic food and holistic medicine, and don’t fall for all the propaganda and fear-mongering spread by the CDC in America. End of story.
the news network 