Vaccine News – VAXXED TV – No more vaccinations for my family & Study – Aluminum in the central nervous system (CNS): toxicity in humans and animals, vaccine adjuvants, and autoimmunity

International journal of science – 05.Sep.2013

Study – Topoisomerases facilitate transcription of long genes linked to autism

Abstract
Topoisomerases are expressed throughout the developing and adult brain and are mutated in some individuals with autism spectrum disorder (ASD). However, how topoisomerases are mechanistically connected to ASD is unknown. Here we find that topotecan, a topoisomerase 1 (TOP1) inhibitor, dose-dependently reduces the expression of extremely long genes in mouse and human neurons, including nearly all genes that are longer than 200 kilobases. Expression of long genes is also reduced after knockdown of Top1 or Top2b in neurons, highlighting that both enzymes are required for full expression of long genes. By mapping RNA polymerase II density genome-wide in neurons, we found that this length-dependent effect on gene expression was due to impaired transcription elongation. Interestingly, many high-confidence ASD candidate genes are exceptionally long and were reduced in expression after TOP1 inhibition. Our findings suggest that chemicals and genetic mutations that impair topoisomerases could commonly contribute to ASD and other neurodevelopmental disorders.

Immunologic research – Jul.2013

Study – Aluminum in the central nervous system (CNS): toxicity in humans and animals, vaccine adjuvants, and autoimmunity

Authors and affiliations
C. A. Shaw – 1,2,3
L. Tomljenovic – 1
1.Neural Dynamics Research Group, Department of Ophthalmology and Visual SciencesUniversity of British Columbia (UBC)VancouverCanada
2.Program in Experimental MedicineUniversity of British Columbia (UBC)VancouverCanada
3.Program in NeuroscienceUniversity of British Columbia (UBC)VancouverCanada

Abstract
We have examined the neurotoxicity of aluminum in humans and animals under various conditions, following different routes of administration, and provide an overview of the various associated disease states. The literature demonstrates clearly negative impacts of aluminum on the nervous system across the age span. In adults, aluminum exposure can lead to apparently age-related neurological deficits resembling Alzheimer’s and has been linked to this disease and to the Guamanian variant, ALS–PDC. Similar outcomes have been found in animal models. In addition, injection of aluminum adjuvants in an attempt to model Gulf War syndrome and associated neurological deficits leads to an ALS phenotype in young male mice. In young children, a highly significant correlation exists between the number of pediatric aluminum-adjuvanted vaccines administered and the rate of autism spectrum disorders. Many of the features of aluminum-induced neurotoxicity may arise, in part, from autoimmune reactions, as part of the ASIA syndrome.

US National Library of Medicine
National Institutes of Health – Jun 2014

Study – Transcriptomic analyses of neurotoxic effects in mouse brain after intermittent neonatal administration of thimerosal.

Li X, Qu F, Xie W, Wang F, Liu H, Song S, Chen T, Zhang Y, Zhu S, Wang Y, Guo C, Tang TS.
Author information
State Key Laboratory of Biomembrane and Membrane Biotechnology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.

Abstract
Thimerosal is a vaccine antimicrobial preservative which has long been suspected an iatrogenic factor possibly contributing to neurodevelopmental disorders including autism. The association between infant vaccine thimerosal exposure and autism remains an open question. Although thimerosal has been removed from mandatory childhood vaccines in the United States, thimerosal-preserved vaccines are still widely used outside of the United States especially in developing countries. Notably, thimerosal-containing vaccines are being given to the newborns within the first 12-24 h after birth in some countries. To examine the possible neurotoxic effects of early neonatal exposure to a higher level of thimerosal, FVB mice were subcutaneously injected with thimerosal-mercury at a dose which is 20× higher than that used for regular Chinese infant immunization during the first 4 months of life. Thimerosal-treated mice exhibited neural development delay, social interaction deficiency, and inclination of depression. Apparent neuropathological changes were also observed in adult mice neonatally treated with thimerosal. High-throughput RNA sequencing of autistic-behaved mice brains revealed the alternation of a number of canonical pathways involving neuronal development, neuronal synaptic function, and the dysregulation of endocrine system. Intriguingly, the elevation of anterior pituitary secreting hormones occurred exclusively in male but not in female thimerosal-treated mice, demonstrating for the first time the gender bias of thimerosal-mercury toxicity with regard to endocrine system. Our results indicate that higher dose of neonatal thimerosal-mercury (20× higher than that used in human) is capable of inducing long-lasting substantial dysregulation of neurodevelopment, synaptic function, and endocrine system, which could be the causal involvements of autistic-like behavior in mice.

VAXXED TV – Your Findings Are Only As Good As Your Data

Dental health connection

Government failure

MMR devastated my son

I refuse to vaccinate anyone

Vaxxed versus unvaxxed in my home

No more vaccinations for my family

Vaccines gave my son autism

Following Wayne!

DAD WANTED ME TO BE SURE

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ONE FOR ISRAEL Ministry – Jewish Johnathan Ben-David forgave his killer and you would not believe why!!!

How to accept Jesus Christ as your personal Saviour

Testimony by Phil Robertson from Duck Dynasty

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.

Isaiah 53 – Old testament Prophecy about Jesus

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.

 

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Vaccine News – VAXXED TV – Vaccines injured my son & Study – Thiol-modulated mechanisms of the cytotoxicity of thimerosal and inhibition of DNA topoisomerase II alpha

US National Library of Medicine
National Institutes of Health – Feb 2012

Study – Mechanisms of aluminum adjuvant toxicity and autoimmunity in pediatric populations.

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.

The spectrum of ASIA: ‘Autoimmune (Auto-inflammatory) Syndrome induced by Adjuvants’

Sage journals – 1 Feb 2012

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

Study – Etiology of autism spectrum disorders: Genes, environment, or both?

C Shaw, S Sheth, D Li, L Tomljenovic

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

Study – Thiol-modulated mechanisms of the cytotoxicity of thimerosal and inhibition of DNA topoisomerase II alpha.

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

Vaxxed versus unvaxxed

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ONE FOR ISRAEL Ministry – Jewish Johnathan Ben-David forgave his killer and you would not believe why!!!

How to accept Jesus Christ as your personal Saviour

Testimony by Phil Robertson from Duck Dynasty

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.

Isaiah 53 – Old testament Prophecy about Jesus

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.

 

Vaccine News – Study – Administration of Thimerosal to Infant Rats Increases Overflow of Glutamate and Aspartate in the Prefrontal Cortex: Protective Role of Dehydroepiandrosterone Sulfate & VAXXED TV – My son has autism from the MMR

US National Library of Medicine
National Institutes of Health – 2011

Study – Aluminum vaccine adjuvants: are they safe?

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

Study – Induction of metallothionein in mouse cerebellum and cerebrum with low-dose thimerosal injection.

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

Study – Administration of Thimerosal to Infant Rats Increases Overflow of Glutamate and Aspartate in the Prefrontal Cortex: Protective Role of Dehydroepiandrosterone Sulfate

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

Vit K gave my son eczema

My son has autism from the MMR

Vaccine injury testimony

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How to accept Jesus Christ as your personal Saviour

Testimony by Phil Robertson from Duck Dynasty

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.

 

Vaccine News – Pig Virus DNA Found in Rotavirus Vaccine & Study – Hepatitis B vaccination of male neonates and autism diagnosis, NHIS 1997-2002

Pig Virus DNA Found in Rotavirus Vaccine

By Daniel J. DeNoon

March 22, 2010 — GlaxoSmithKline’s Rotarix rotavirus vaccine contains DNA from an apparently harmless pig virus, the company and the FDA today announced.
The FDA estimates that 1 million U.S. kids have received the Rotarix vaccine.
The contamination was discovered by researchers developing a new technique for detecting viral material. GlaxoSmithKline confirmed that the pig virus, porcine circovirus type 1 or PCV-1, has been in the vaccine since it was developed.
This means that pig virus DNA was in the vaccine throughout clinical trials. No safety issues emerged from these international studies with 90,000 participants or, GlaxoSmithKline says, in post-marketing surveillance covering more than 69 million doses of the vaccine.
Nevertheless, as a precaution the FDA is asking doctors to stop using the two-dose Rotarix vaccine, which it approved in 2008.
“The message is clearly not a message of safety but of caution going forward,” FDA Commissioner Margaret Hamburg, MD, said at a news conference. “We believe the vaccine is both safe and effective and we strongly encourage vaccination against rotavirus. But we want to more deeply understand the finding of this unexpected material in the product, and that is why we are putting a clinical pause on its use.”

A study published in the Journal Annals of Epidemiology has shown that giving the Hepatitis B vaccine to newborn baby boys could triple the risk of developing an autism spectrum disorder compared to boys who were not vaccinated as neonates. The research was conducted at Stony Brook University Medical Centre, NY.

Study – Hepatitis B vaccination of male neonates and autism diagnosis, NHIS 1997-2002

US National Library of Medicine
National Institutes of Health – 2010

Gallagher CM, Goodman MS.
Author information
PhD Program in Population Health and Clinical Outcomes Research, Stony Brook University Medical Center, State University of New York at Stony Brook, Stony Brook, New York, USA. cmgallagher@notes.cc.sunysb.edu

Abstract
Universal hepatitis B vaccination was recommended for U.S. newborns in 1991; however, safety findings are mixed. The association between hepatitis B vaccination of male neonates and parental report of autism diagnosis was determined. This cross-sectional study used weighted probability samples obtained from National Health Interview Survey 1997-2002 data sets. Vaccination status was determined from the vaccination record. Logistic regression was used to estimate the odds for autism diagnosis associated with neonatal hepatitis B vaccination among boys age 3-17 years, born before 1999, adjusted for race, maternal education, and two-parent household. Boys vaccinated as neonates had threefold greater odds for autism diagnosis compared to boys never vaccinated or vaccinated after the first month of life. Non-Hispanic white boys were 64% less likely to have autism diagnosis relative to nonwhite boys. Findings suggest that U.S. male neonates vaccinated with the hepatitis B vaccine prior to 1999 (from vaccination record) had a threefold higher risk for parental report of autism diagnosis compared to boys not vaccinated as neonates during that same time period. Nonwhite boys bore a greater risk.

A study published in the Journal of Inorganic Biochemistry by researchers at the Neural Dynamics Group, Department of Ophthalmology and Visual Sciences at the University of British Columbia determined that Aluminum, a highly neurotoxic metal and the most commonly used vaccine adjuvant may be a significant contributing factor to the rising prevalence of ASD in the Western World. They showed that the correlation between ASD prevalence and the Aluminum adjuvant exposure appears to be the highest at 3-4 months of age. The studies also show that children from countries with the highest ASD appear to have a much higher exposure to Aluminum from vaccines. The study points out that several prominent milestones of brain development coincide with major vaccination periods for infants. These include the onset of synaptogenesis (birth), maximal growth velocity of the hippocampus and the onset of amygdala maturation. Furthermore, major developmental transition in many bio-behavioural symptoms such as sleep, temperature regulation, respiration and brain wave patterns, all of which are regulated by the neuroendocrine network. Many of these aspects of brain function are known to be impaired in autism, such as sleeping and brain wave patterns.

Study – Do aluminum vaccine adjuvants contribute to the rising prevalence of autism?

Journal of Inorganic Biochemistry – 14 Aug 2011

Lucija Tomljenovic a,
Christopher A. Shaw a,b
a Neural Dynamics Research Group, Department of Ophthalmology and Visual Sciences, University of British Columbia, 828 W. 10th Ave, Vancouver, BC, Canada V5Z 1L8
b Departments of Ophthalmology and Visual Sciences and Experimental Medicine and the Graduate Program in Neuroscience, University of British Columbia, Vancouver, British Columbia, 828 W. 10th Ave, Vancouver, BC, Canada V5Z 1L8

Abstract:
Autism spectrum disorders (ASD) are serious multisystem developmental disorders and an urgent global public health concern. Dysfunctional immunity and impaired brain function are core deficits in ASD. Aluminum (Al), the most commonly used vaccine adjuvant, is a demonstrated neurotoxin and a strong immune stimulator. Hence, adjuvant Al has the potential to induce neuroimmune disorders. When assessing adjuvant toxicity in children, two key points ought to be considered:
(i) children should not be viewed as “small adults” as their unique physiology makes them much more vulnerable to toxic insults;
and
(ii) if exposure to Al from only few vaccines can lead to cognitive impairment and autoimmunity in adults, is it unreasonable to question whether the current pediatric schedules, often containing 18 Al adjuvanted vaccines, are safe for children? By applying Hill’s criteria for establishing causality between exposure and outcome we investigated whether exposure to Al from vaccines could be contributing to the rise in ASD prevalence in the Western world.
Our results show that:
(i) children from countries with the highest ASD prevalence appear to have the highest exposure to Al from vaccines;
(ii) the increase in exposure to Al adjuvants significantly correlates with the increase in ASD prevalence in the United States observed over the last two decades (Pearson r=0.92, pb0.0001);
and (iii) a significant correlation exists between the amounts of Al administered to preschool children and the current prevalence of ASD in seven Western countries, particularly at 3–4 months of age (Pearson r=0.89–0.94, p=0.0018–0.0248). The application of the Hill’s criteria to these data indicates that the correlation between Al in vaccines and ASD may be causal. Because children represent a fraction of the population most at risk for complications following exposure to Al, a more rigorous evaluation of Al adjuvant safety seems warranted

According to the FDA, vaccines represent a special category of drugs as they are generally given to healthy individuals. Further according to the FDA, “this places significant emphasis on their vaccine safety”. While the FDA does set an upper limit for Aluminum in vaccines at no more that 850/mg/dose, it is important to note that this amount was selected empirically from data showing that Aluminum in such amounts enhanced the antigenicity of the vaccine, rather than from existing safety. Given that the scientific evidence appears to indicate that vaccine safety is not as firmly established as often believed, it would seem ill advised to exclude paediatric vaccinations as a possible cause of adverse long-term neurodevelopment outcomes , including those associated with autism.

VAXXED TV – My brother has autism from vaccines

I’m a pharmacist and I will never vaccinate again

Vaccines caused my daughters autism and epilepsy

My 3 children are unvaccinated

I’m a nurse and I didn’t know

Type 1 diabetes, autoimmunity and vaccines

The one and only Ginger Taylor

Vaccines gave my children autism, tics, allergies and eczema

Vaccines cause ADHD, allergies and anxiety

Vaccines gave my son autism

****************************************************

How to accept Jesus Christ as your personal Saviour

Testimony by Phil Robertson from Duck Dynasty

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.

 

Vaccine News – Study – Association of spontaneous abortion with receipt of inactivated influenza vaccine containing H1N1pdm09 in 2010-11 and 2011-12

Study – Human papilloma virus vaccine and primary ovarian failure: another facet of the autoimmune/inflammatory syndrome induced by adjuvants.

US National Library of Medicine
National Institutes of Health – Oct 2013

Colafrancesco S – 1, Perricone C, Tomljenovic L, Shoenfeld Y.
Author information
1 Zabludowicz Center for Autoimmune Diseases Sheba Medical Center, Tel-Hashomer, Israel; Rheumatology Unit, Department of Internal Medicine and Medical Specialities, Sapienza University of Rome, Rome, Italy.

Abstract
PROBLEM:
Post-vaccination autoimmune phenomena are a major facet of the autoimmune/inflammatory syndrome induced by adjuvants (ASIA) and different vaccines, including HPV, have been identified as possible causes.
METHOD OF STUDY:
The medical history of three young women who presented with secondary amenorrhea following HPV vaccination was collected. Data regarding type of vaccine, number of vaccination, personal, clinical and serological features, as well as response to treatments were analyzed.
RESULTS:
All three patients developed secondary amenorrhea following HPV vaccinations, which did not resolve upon treatment with hormone replacement therapies. In all three cases sexual development was normal and genetic screen revealed no pertinent abnormalities (i.e., Turner’s syndrome, Fragile X test were all negative). Serological evaluations showed low levels of estradiol and increased FSH and LH and in two cases, specific auto-antibodies were detected (antiovarian and anti thyroid), suggesting that the HPV vaccine triggered an autoimmune response. Pelvic ultrasound did not reveal any abnormalities in any of the three cases. All three patients experienced a range of common non-specific post-vaccine symptoms including nausea, headache, sleep disturbances, arthralgia and a range of cognitive and psychiatric disturbances. According to these clinical features, a diagnosis of primary ovarian failure (POF) was determined which also fulfilled the required criteria for the ASIA syndrome.
CONCLUSION:
We documented here the evidence of the potential of the HPV vaccine to trigger a life-disabling autoimmune condition. The increasing number of similar reports of post HPV vaccine-linked autoimmunity and the uncertainty of long-term clinical benefits of HPV vaccination are a matter of public health that warrants further rigorous inquiry.

Study – Association of spontaneous abortion with receipt of inactivated influenza vaccine containing H1N1pdm09 in 2010-11 and 2011-12.

US National Library of Medicine
National Institutes of Health – Sep 2017

Donahue JG – 1, Kieke BA – 2, King JP – 3, DeStefano F – 4, Mascola MA – 5, Irving SA – 6, Cheetham TC – 7, Glanz JM – 8, Jackson LA – 9, Klein NP – 10, Naleway AL – 11, Weintraub E – 12, Belongia EA – 13.
Author information
1 Marshfield Clinic Research Institute, 1000 N. Oak Ave, Marshfield, WI 54449, United States. Electronic address: donahue.james@mcrf.mfldclin.edu.
2 Marshfield Clinic Research Institute, 1000 N. Oak Ave, Marshfield, WI 54449, United States. Electronic address: kieke.burney@mcrf.mfldclin.edu.
3 Marshfield Clinic Research Institute, 1000 N. Oak Ave, Marshfield, WI 54449, United States. Electronic address: king.jennifer@mcrf.mfldclin.edu.
4 Centers for Disease Control and Prevention, Immunization Safety Office, 1600 Clifton Road NE, MS-D26 Atlanta, GA 30333, United States. Electronic address: fxd1@cdc.gov.
5 Marshfield Clinic, Department of Obstetrics and Gynecology, 1000 N. Oak Ave, Marshfield, WI 54449, United States. Electronic address: mascola.maria@marshfieldclinic.org.
6 Kaiser Permanente Northwest, 3800 N. Interstate Ave, Portland, OR 97227, United States. Electronic address: stephanie.a.irving@kpchr.org.
7 Kaiser Permanente Southern California, 100 S. Los Robles Ave., 2nd Floor, Pasadena, CA 91101, United States. Electronic address: craig.t.cheetham@kp.org.
8 Kaiser Permanente Colorado, 10065 E. Harvard, Suite 300, Denver, CO 80231, United States. Electronic address: jason.m.glanz@kp.org.
9 Group Health Research Institute, 1730 Minor Avenue, Suite 1600, Seattle, WA 98101, United States. Electronic address: jackson.l@ghc.org.
10 Kaiser Permanente Northern California, 1 Kaiser Plaza, 16th Floor, Oakland, CA 94612, United States. Electronic address: Nicola.Klein@kp.org.
11 Kaiser Permanente Northwest, 3800 N. Interstate Ave, Portland, OR 97227, United States. Electronic address: Allison.Naleway@kpchr.org.
12 Centers for Disease Control and Prevention, Immunization Safety Office, 1600 Clifton Road NE, MS-D26 Atlanta, GA 30333, United States. Electronic address: eiw8@cdc.gov.
13 Marshfield Clinic Research Institute, 1000 N. Oak Ave, Marshfield, WI 54449, United States. Electronic address: belongia.edward@marshfieldclinic.org.

Abstract

INTRODUCTION:
Inactivated influenza vaccine is recommended in any stage of pregnancy, but evidence of safety in early pregnancy is limited, including for vaccines containing A/H1N1pdm2009 (pH1N1) antigen. We sought to determine if receipt of vaccine containing pH1N1 was associated with spontaneous abortion (SAB).
METHODS:
We conducted a case-control study over two influenza seasons (2010-11, 2011-12) in the Vaccine Safety Datalink. Cases had SAB and controls had live births or stillbirths and were matched on site, date of last menstrual period, and age. Of 919 potential cases identified using diagnosis codes, 485 were eligible and confirmed by medical record review. Exposure was defined as vaccination with inactivated influenza vaccine before the SAB date; the primary exposure window was the 1-28days before the SAB.
RESULTS:
The overall adjusted odds ratio (aOR) was 2.0 (95% CI, 1.1-3.6) for vaccine receipt in the 28-day exposure window; there was no association in other exposure windows. In season-specific analyses, the aOR in the 1-28days was 3.7 (95% CI 1.4-9.4) in 2010-11 and 1.4 (95% CI 0.6-3.3) in 2011-12. The association was modified by influenza vaccination in the prior season (post hoc analysis). Among women who received pH1N1-containing vaccine in the previous influenza season, the aOR in the 1-28days was 7.7 (95% CI 2.2-27.3); the aOR was 1.3 (95% CI 0.7-2.7) among women not vaccinated in the previous season. This effect modification was observed in each season.
CONCLUSION:
SAB was associated with influenza vaccination in the preceding 28days. The association was significant only among women vaccinated in the previous influenza season with pH1N1-containing vaccine. This study does not and cannot establish a causal relationship between repeated influenza vaccination and SAB, but further research is warranted.

VAXXED TV – My son seized on the table after vaccines #vaxxed #DidYouKnow #Praybig

My 2 month old son died following vaccinations #vaxxed #DidYouKnow #Praybig

Mandates would have killed my son #vaxxed #DidYouKnow #Praybig

One of my children is vaccinated and one is not #vaxxed #DidYouKnow #Praybig

Vaccinated without my consent #vaxxed #DidYouKnow #Praybig

Vaccines injured my family #vaxxed #DidYouKnow #Praybig

Flu shot injured me #vaxxed #DidYouKnow #Praybig

My son has autism from vaccines #vaxxed #DidYouKnow #Praybig

Vaccines destroyed my family #vaxxed #DidYouKnow #praybig

The medical profession killed my son #vaxxed #DidYouKnow #Praybig

 

How to accept Jesus Christ as your personal Saviour

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.

 

Vaccine News – VAXXED TV – I’ve waited 30 years to tell my story

Vaccines are NOT the cause of SIDS…except when the federal government says they are and compensates parents accordingly (this is a ruling from last month, July 2017):

“After carefully analyzing and weighing all of the evidence and testimony presented in this case in accordance with the applicable legal standards, the undersigned finds that petitioners have met their legal burden. Petitioners have put forth preponderant evidence that the vaccines J.B. received on September 2, 2011 actually caused or substantially contributed to his death from Sudden Infant Death Syndrome. Furthermore, respondent has failed to put forth preponderant evidence that J.B.’s death was in fact caused by factors unrelated to the vaccines. Accordingly, petitioners are entitled to compensation.”
https://ecf.cofc.uscourts.gov/cgi-bin/show_public_doc?2013vv0611-73-0
In the United States Court of Federal Claims
OFFICE OF SPECIAL MASTERS
Filed: July 10, 2017
Entitlement Decision; Diphtheria Tetanus-acellular Pertussis (DTaP) Vaccine; Inactivated Polio Vaccine AND HUMAN SERVICES,(IPV); Haemophilus Influenzae(HiB)Vaccine; Pneumococcal Conjugate(PCV) Vaccine; Rotavirus Vaccine;Sudden Infant Death Syndrome (SIDS).

RULING ON ENTITLEMENT
On August 27, 2013, Chase Boatmon and Maurina Cupid (“petitioners”), as the representatives of the estate of their deceased minor child, J.B.,filed a petition under the National Vaccine Injury Compensation Program (“Vaccine Act” or the “Program”),342 U.S.C. § 300aa-10 et. seq. (2012). Petitioners allege that as a result of receiving vaccinations for
Diphtheria-Tetanus-acellular Pertussis (“DTaP”), inactivated polio (“IPV”), haemophilus influenzae(“HiB”), Pneumococcal Conjugate (“PCV”), and Rotavirus vaccinations on September 2, 2011, J.B. passed away from Sudden Infant Death Syndrome (“SIDS”) on September 3, 2011.
See Petition (ECF No. 1);Amended Petition(ECF No. 15).After carefully analyzing and weighing all of the evidence and testimony presented in this case in accordance with the applicable legal standards, the undersigned finds that petitioners have met their legal burden.

Petitioners have put forth preponderant evidence that the vaccines J.B. received on September 2, 2011 actually caused or substantially contributed to his deathfrom Sudden Infant Death Syndrome. Furthermore, respondent has failed to put forth preponderant evidence that J.B.’s death was in fact caused by factors unrelated to the vaccines. Accordingly, petitioners are entitled to compensation.

Study – Human papilloma virus vaccine and primary ovarian failure: another facet of the autoimmune/inflammatory syndrome induced by adjuvants.
RESULTS: All three patients developed secondary amenorrhea following HPV vaccinations, which did not resolve upon treatment with hormone replacement therapies. In all three cases sexual development was normal and genetic screen revealed no pertinent abnormalities (i.e., Turner’s syndrome, Fragile X test were all negative). Serological evaluations showed low levels of estradiol and increased FSH and LH and in two cases, specific auto-antibodies were detected (antiovarian and anti thyroid), suggesting that the HPV vaccine triggered an autoimmune response. Pelvic ultrasound did not reveal any abnormalities in any of the three cases. All three patients experienced a range of common non-specific post-vaccine symptoms including nausea, headache, sleep disturbances, arthralgia and a range of cognitive and psychiatric disturbances. According to these clinical features, a diagnosis of primary ovarian failure (POF) was determined which also fulfilled the required criteria for the ASIA syndrome.
CONCLUSION: We documented here the evidence of the potential of the HPV vaccine to trigger a life-disabling autoimmune condition. The increasing number of similar reports of post HPV vaccine-linked autoimmunity and the uncertainty of long-term clinical benefits of HPV vaccination are a matter of public health that warrants further rigorous inquiry.

#VaXism NEWS A REAL journalist, Liz Gunn, interviews Dr Suzanne Humphries

VAXXED TV – 4 month vaccinations killed my baby

VAXXED TV – Dr Jeremy Kobler

VAXXED TV – Gardasil HPV vaccine killed my daughter

 

VAXXED TV – Multiple injuries in my family

VAXXED TV – I’ve waited 30 years to tell my story

VAXXED TV – What My Parents Went Through Is Heartbreaking

VAXXED TV – Entire Family Injured

VAXXED TV – Interview in a hospital with Sarah Cox

VAXXED TV – Feilding, New Zealand VAXXED vs. UNVAXXED

VAXXED TV – Palmerston North – Vaxxed versus unvaccinated

HighWire with Del Bigtree Live Stream

Master Manipulator: The Explosive True Story of Fraud, Embezzlement, and Government Betrayal at the CDC

Story at-a-glance
Book by investigative journalist reveals how the U.S. Centers for Disease Control and Prevention (CDC) has engaged in massive fraud, misinformation and manipulation of vaccine information
A Danish scientist hired by the CDC to investigate the vaccine-autism link was charged with 22 counts of fraud and theft, yet the U.S. has not bothered to extradite him from Denmark, where he can be easily found
Most doctors will tell you the science is settled; there’s no link between vaccines and autism. In reality, the CDC is well aware there’s a link. Suppression of such data is why so few doctors understand the problem

VaxXed Arizona – Weston and Emily Wyatt Vaccine Injury
Weston and Emily are vaccine injured. Weston received 20+ vaccines in 4 months before he was 6 months old. He is now 19 and functions at the level of a 3 year old. Emily is 17 and functions at the level of an 8 year old. Both will require a lifetime of care and support.
Investigate before you vaccinate!

AutismOne Media – Dr Arthur Krigsman -Autism Associated Enterocolitis. Does my child have it? What Can I Do About It?
Dr. Arthur Krigsman presents an up-to-the minute report on what has been learned about determining a child’s gastrointestinal health status via innovative and objective laboratory testing, with corresponding information about helpful steps to take should test results evidence pathology and/or dysfunction.

AutismOne Media – Autism Associated Enterocolitis 2016 – Arthur Krigsman, MD
Gastrointestinal symptoms are exceedingly common in children with autism and are known to be associated with the severity of ASD behaviors. Parents and caregivers often underestimate or fail to recognize GI symptoms because of the focus on behaviors, cognition, and speech. However, recognition, evaluation, and treatment of GI symptoms, particularly autism-associated enterocolitis, often improves not only the child’s GI symptoms, but also cognition and behavior as well. This lecture uses photographs and videos of affected children (facial features removed) to demonstrate GI symptoms in this poorly communicative patient group as well as demonstrating actual images of ASD-associated GI inflammatory pathology obtained at endoscopy and biopsy. The unique features of ASD-associated enterocolitis that together comprise a new disease entity will be presented. Proposed therapeutic interventions will be discussed.

HPV Gardasil vaccine injured my daughter #vaxxed #Praybig

EVZ – SFÂŞIAT DE DURERE pentru că sistemul sanitar din ROMÂNIA i-a UCIS copilul, un TATĂ face o RADIOGRAFIE LUCIDĂ a GENOCIDULUI împotriva românilor. “Indivizi cu MENTALITATE de ASASINI conduc sistemul sanitar”
Înainte de a fi deranjați de această temă am însă o rugăminte către dvs : întrebați-i pe acești experți cine și unde verifică in această țară compoziția și siguranța (contaminat versus necontaminat) vaccinurilor importate integral și injectate în organismul copiilor noștri.
Iar dacă experții vă vor comunica că această verificare se face de către Agenția Națională a Medicamentului și a Dispozitivelor Medicale (ANMDM), atunci să stiți că sunteți mințiti în mod grotesc.
Sunteți mințiți la fel de grotesc cum am fost mințiți (de către un fost consilier al unui fost ministru al Sănătății) toți cei care am participat recent la o conferință organizată de către Ministerul Sănătății pe tema vaccinării.
Acest fost consilier (care ne-a mințit fără nici o reținere afirmând că în România ANMDM verifică ”lot cu lot” vaccinurile injectate copiilor noștri) continuă să ceară în mod public instaurarea unei dictaturi medicale și vaccinarea cu forța a copiilor chiar dacă nimeni nu verifică aceste vaccinuri în România (tot așa cum nimeni nu a verificat in această țară dezinfectanții utilizați in spitale) și nici nu garantează nimeni (nici măcar companiile farmaceutice care le produc) pentru siguranța lor.
Conform unui răspuns oficial oferit la o solicitare a APC România, ANMDM a confirmat că ei nu testează și nu verifică vaccinurile importate și ulterior injectate în organismul copiilor noștri.
Eu nu vă spun să nu vă vaccinati copiii sau sa-i vaccinati, eu vă rog doar să nu uitați niciodată că această decizie este și trebuie să ramână a fiecărui părinte, fără să existe nici un fel de presiuni sau amenințări halucinante precum amenințarea cu interzicerea accesului la educație pentru un copil nevaccinat, decăderea din drepturile părintești pentru cei care nu mai au în mod argumentat încredere în siguranța actualelor vaccinuri și răpirea copiilor lor din mijlocul familiei (preluarea copiilor de către așa zisa Protecție a Copilului), urmată de trimiterea lor într-un orfelinat sau darea lor în adopție în urma unei posibile hotarâri judecătorești în acest sens

 

Vaccine News – Vaccine Mechanisms in Autism

 

Truth from “a real doctor” about vaccines, both medically and the business of running a medical clinic without accepting the bribes for vaccinating children.

Six doctors who have administered vaccines in their practice are all asked the same question. When you were in medical school, how much education regarding vaccines was provided before you were permitted to administer them?
Interviews, camera and editing by Joshua Coleman.

Our 8 Unvaccinated children are super healthy #vaxxed #prayBig #PeoplesStudy #truth #science

Newborn baby dies after receiving eight vaccinations on schedule; pathologists confirm vaccines responsible for death
A mother from Michigan has gone through an emotional journey in finding exactly what caused her son to mysteriously die.
What she uncovered is another case added to the excessive vaccination-induced early death.
Elijah Daniel French was born on May 4, 2007, and had mysteriously died a couple days after receiving 8 routine vaccinations, as recommended by the Centers for Disease Control and Prevention (CDC) for childhood vaccination. This was determined by child death investigator and many pathologists to have been a result from vaccination.
According to VacTruth.com: Baby Elijah was happy, healthy, and smiling until he underwent routine vaccinations. His health began to worsen, and ended up developing a high fever and breathing problems.
In the family account, it was noted that Danny had been vaccinated for seven other conditions at 5 1/2 months old, including hepatitis B, DTaP, Hib, pneumococcal and polio vaccines. To make things worse, a few months later he was brought over to the doctor’s office where he was administered a second round of the same vaccines. This caused him to develop asthma and exacerbated his problems even more.
Daniel’s mother didn’t know what else to do, other than see a doctor for her Childs condition. So, she brought Daniel back to the doctor’s office where ehe was given a third round of vaccines at 14 months old. He was administered 8 vaccines in 4 injections: Varicella, Hib, DTaP and MMR (measles, mumps, and rubella). This is when Daniel’s started to dramatically worsen.
“That night, Danny was still eating and drinking but was cranky and slept more than usual,” his mother reported.
“By the next day, he was extremely fatigued, irritable and had a loss of appetite. He did not have a fever at this time. He was red and warm where they injected him. These symptoms only worsened.”
“By the third day, Danny was unable to stay awake for longer than thirty minutes, he had zero food intake, his fluid intake diminished and he cried excessively. Seventy-one hours after his doctor visit, Danny developed a fever from the vaccines and was given Children’s Tylenol. His doctor was called but there was no answer from him because it was the July 4th holiday, the office was closed.”
Three independent pathologists confirm that young Danny’s death was caused by vaccines

Infant Accidentally Vaccinated with Gardasil – Mother Blamed for Vaccine Injuries and Baby Medically Kidnapped
June 29, 2017
by Health Impact News/MedicalKidnap.com Staff
Doctors call it a “medication administration error.” During a routine check-up at her pediatrician’s office, 4-month old Aniya was accidentally given the Gardasil 9 vaccine, and she hasn’t been the same since.
Anita Vasquez of Victoria, Texas, herself a nurse, says that “doctors are in denial” that any of the medical issues that began after her daughter received the shot are related to the vaccine.
Aniya was a happy and healthy breastfed baby before her 4-month doctor visit. Her only illness was an ear infection which had been cleared up with antibiotics shortly before that fateful day of December 29, 2016. Since then, she has suffered numerous health issues and several hospitalizations.
Rather than acknowledge the possibility that the Gardasil 9 vaccine contributed to the decline in Aniya’s health, doctors and Child Protective Services have reportedly blamed the mother. Her desperate search for answers has led instead to her being accused of Munchausen by Proxy, or “medical child abuse,” and her baby has been seized by the Texas Department of Family and Protective Services (DFPS).
Anita told Health Impact News that her concerns about the vaccine have been dismissed and ignored by virtually everyone involved in her daughter’s care. DFPS refers to her “unfounded concerns” about the Gardasil 9 vaccine. She believes that they are trying to cover up the dangers of the vaccine.
This is any mother’s worst nightmare, and no one deserves this.
Distracted Doctor Administers Wrong Vaccine – Infant Received 8 Vaccines at Same Visit
The Vasquez family nightmare began when Anita took her 13 year old son and her 4 month old baby girl to a routine check-up.
Anita is a registered nurse by trade, and she didn’t question the recommended vaccinations. Her son was to receive the Gardasil 9 vaccine, and her daughter was to receive 2 shots and an oral vaccine. The nurse drew up and labeled the vaccines and placed the syringes in a single envelope.
Anita says that Dr. Veronica Guel-Valdivia came into the room talking on her cell phone. When the doctor finished her phone conversation, she asked Anita to put baby Aniya on the table.

Polio Paralyzes 17 Children in Syria, W.H.O. Says
Unlike Syria’s first polio outbreak in 2013, caused by a wild strain that paralyzed 36 children before it was brought under control, the new outbreak derived from the polio vaccine itself, Mr. Jasarevic said.
The vaccine, a weakened form of the polio virus that triggers the immune system’s response, is secreted in the waste of vaccinated children, and over time can mutate into an infectious strain that may afflict the unvaccinated. The risks are especially high in areas where not all children have received the vaccine and where the mutated virus can spread from contaminated sewage or water.
“These vaccine-derived outbreaks really are a marker of poor vaccination and poor sanitation in the community,” said Dr. Homer Venters, director of programs at Physicians for Human Rights, an international aid group based in New York that supports humanitarian work in war zones, including Syria and Yemen.

After receiving a flu shot, this beautiful young girl suffered vaccine-induced paralysis, also known as Transverse Myeltis, one of many labels given to our modern-day “Polio”, which was never eradicated by vaccines and in fact, is many times directly caused by them.
What else aren’t you being told? Find out here, while this groundbreaking, 9-part docu-series is still free>>> tinyurl.com/9Episodes
Guillain-Barré Syndrome is another label given to this paralysis, very often caused by vaccines.
More info here: vactruth.com/2012/04/25/change-names-of-diseases
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Flu Vaccine Efficacy Slips From Prior Estimate, CDC Says
Robert Lowes
June 23, 2017
The influenza vaccine for the 2016-2017 season was 42% effective in preventing an infection from any A or B virus in people of all ages, down from a preliminary estimate of 48% in February, the Centers for Disease Control and Prevention (CDC) announced earlier this week.
The CDC frames the effectiveness rating in terms of reducing a vaccinated person’s risk of getting sick and having to visit a clinician on an outpatient basis because of the flu.
The vaccine worked the best among children aged 6 months to 8 years, at 61%, and the least among individuals aged 18 to 49 years, at 19%. For people aged 65 years or older — a demographic group that’s especially vulnerable to the flu — effectiveness stood at 25%.
The CDC reported the efficacy rates at a meeting of its Advisory Committee on Immunization Practices (ACIP) in Atlanta, Georgia, on June 21 and 22.
Vaccine effectiveness varied considerably by influenza virus type. It was at its lowest in all age groups — 34% — for the A/H3N2 virus that dominated this season. Performance picked up for the A/H1N1 pandemic virus (54%), the B/Yamagata virus (55%), and the B/Victoria virus (60%), according to epidemiologist Jill Ferdinands, PhD, in the CDC’s Influenza Division.
The CDC adjusts its efficacy estimates for such factors as age, sex, and underlying medical conditions.
The 42% overall effectiveness of the latest influenza vaccine is somewhat lower than the 47% for the 2015-2016 vaccine, but a big improvement over the 23% for the 2014-2015 edition. Vaccine performance suffers when the viruses they’re designed to thwart undergo genetic drift after the vaccine is formulated. However, the CDC reported that most of the flu viruses in circulation in 2016-2017 were similar to those in the latest vaccine, which came in trivalent and quadrivalent formulas.

The prenatal flu vaccine and ASD: Good research, bad conclusions.
Brian S. Hooker, Ph.D.
June 23, 2017
Very early this year, a research group from the insurance giant Kaiser Permanente published a paper concluding no evidence of harm in administering prenatal influenza vaccines. The study authors asserted that there was no relationship between those who received the flu shot during pregnancy and later autism spectrum disorder (ASD) diagnosis in the child. However, that proclamation was not consistent with the study’s results. Specifically, women who received the vaccine during their first trimester of pregnancy showed a 20% greater risk of having the child later develop ASD. This was based on a sampling of 13,477 women who received the maternal flu shot in the first trimester, resulting in 260 ASD cases, versus 151,698 “control” women who received no flu shot during pregnancy, resulting in 2,338 ASD cases. This result was statistically significant with a p value of 0.01, which in this case means that the possibility that this is a “chance” finding and not a “true” association was just 1%. In other words, the chances of this being a “true” association are 99%.
In statistics, the gold standard “cut-off” to determine statistical significance is actually a higher p value of 0.05, meaning that the possibility of a chance association is less than 5%. Thus, the first trimester flu shot – ASD relationship should have been deemed statistically significant, with p=0.01, and accordingly a policy change should have been made to suspend use of that vaccine, at least in the first trimester of pregnancy.
However, the study authors instead reached into their statistical “bag of tricks” and trotted out what is termed the “Bonferroni” adjustment. This adjustment is applied in statistics only under very specific instances, when multiple, unrelated statistical evaluations are made using a single data sampling. In this adjustment, simply, the p value is adjusted by multiplying its original value with the number of “independent” evaluations completed in the study of that single data set (Bland et al. 1995 BMJ 310:170). In the case of Zerbo et al. 2017, there were 8 evaluations completed (4 evaluations regarding the flu shot and 4 evaluations regarding women who actually contracted the flu during pregnancy) and thus the original p value of 0.01 was adjusted to 0.08, above the “cut off” value used for deeming “statistical significance.” The Zerbo et al. authors rounded the result up to p=0.1, further moving the result away from the “magic” 0.05 cut-off level, causing the significant result to disappear.
There’s a huge problem here, however, which I pointed out in my letter to the editor of the journal (Hooker 2017 JAMA Pediatrics 171:600) published in their June 2, 2017 edition. The Bonferroni adjustment, among other corrections for multiple, independent comparisons, should not be applied to statistics when there is any interdependence within the different evaluations completed within the data sample. In this case, 4 of the evaluations completed dealt specifically with the timing of the maternal flu shot (first, second and third trimesters, as well as overall risk at any point in pregnancy) and subsequent ASD incidence. So, not only were these four trials all focused on an ASD outcome, but they all dealt with different phases of pregnancy, which were then summed to develop an “overall” risk at any phase of pregnancy. By definition, these trials were anything but statistically independent. An example of an independent evalution would be polling different groups of college students for their tastes in music, food, art, and perhaps health care practices, where none of the preferences could be empirically tied to the next.

Study – Association Between Influenza Infection and Vaccination During Pregnancy and Risk of Autism Spectrum Disorder
January 2, 2017

 

Spokane WA parents report on their vaccinated and Unvaccinated children #vaxxed #peoplesStudy #praybig #truth #science

Don’t Vaccinate to Protect My Cancer Kid
Posted on February 10, 2015
I read with great interest the recent ‘measles epidemic’ articles that addressed the vaccine debate from the point of view of a cancer parent. My interest is the result of being a cancer parent myself – my little girl has been battling leukemia on and off for the past 10 years. I read these articles, and I became angry. Very, very angry. Once again, the government and drug companies are exploiting the plight of children stricken by cancer to achieve a profit-driven end without actually helping them. In fact, this profitable end could cause great harm, even increasing the rates of pediatric leukemia, if their obvious goal of a federally mandated vaccination protocol is achieved. I am a seasoned Momcologist, a term the research-driven cancer parents call themselves. We are the cancer equivalent of Thinking Moms, critical thinkers. I have done extensive reading on the etiology of leukemia, its connection to autoimmune disease, and how vaccines and natural disease may influence these sorts of childhood illnesses. Come connect the dots with me.
Clearly, I empathize with the raw fear the parents in these articles have that their immunocompromised children may contract an illness that could be devastating. I have walked for years in their shoes. I get it. However, the parents in these articles are either grossly misinformed, or their comments have been edited with bias. Let’s get some facts straight about cancer treatment and infection. One of the first things we were warned about after my daughter’s diagnosis was live-virus vaccination. No one in the family was to receive a live-virus vaccine while my daughter was on treatment because these viruses can and do shed (1, 2, 3, 4), some for as much as four weeks (5), potentially infecting the immunocompromised patient with disastrous results. That includes the measles vaccine (MMR II and ProQuad), the intranasal flu vaccine, and the chicken pox shot. In fact, my other children were able to get medical waivers not to receive vaccines because of my daughter’s illness. I know my child is much more likely to encounter a peer at school who has been recently vaccinated with a live-virus vaccine than she is to encounter natural disease from an unvaccinated child.

Mutant Strains Of Polio Vaccine Now Cause More Paralysis Than Wild Polio
June 28, 20173:22 PM ET
For the first time, the number of children paralyzed by mutant strains of the polio vaccine are greater than the number of children paralyzed by polio itself.
So far in 2017, there have been only six cases of “wild” polio reported anywhere in the world. By “wild,” public health officials mean the disease caused by polio virus found naturally in the environment.
By contrast, there have been 21 cases of vaccine-derived polio this year. These cases look remarkably similar to regular polio. But laboratory tests show they’re caused by remnants of the oral polio vaccine that have gotten loose in the environment, mutated and regained their ability to paralyze unvaccinated children
“It’s actually an interesting conundrum. The very tool you are using for [polio] eradication is causing the problem,” says Raul Andino, a professor of microbiology at the University of California at San Francisco.
The oral polio vaccine used throughout most of the developing world contains a form of the virus that has been weakened in the laboratory. But it’s still a live virus. (This is a different vaccine than the injectable one used in the U.S. and most developed countries. The injectable vaccine is far more expensive and does not contain live forms of the virus.)
Andino studies how viruses mutate. In a study published in March, he and his colleagues found that the laboratory-weakened virus used in the oral polio vaccine can very rapidly regain its strength if it starts spreading on its own. After a child is vaccinated with live polio virus, the virus replicates inside the child’s intestine and eventually is excreted. In places with poor sanitation, fecal matter can enter the drinking water supply and the virus is able to start spreading from person to person.
“We discovered there’s only a few [mutations] that have to happen and they happen rather quickly in the first month or two post-vaccination,” Andino says. “As the virus starts circulating in the community, it acquires further mutations that make it basically indistinguishable from the wild-type virus. It’s polio in terms of virulence and in terms of how the virus spreads.”

New Polio Virus Evolution Insights Could Lead to Improved Vaccine
Blocking ‘Gateway Mutations’ Could Prevent Vaccine from Re-Evolving Virulence
By Nicholas Weiler on March 27, 2017
A relentless vaccination campaign has succeeded in eradicating the polio virus from most of the world, reducing the burden of the disease by 99 percent since the year 2000 and preventing more than 13 million children from contracting the disease, according to World Health Organization estimates. However, in regions where vaccination has remained incomplete, on rare occasions the weakened virus used in the vaccine has evolved the ability to escape the vaccinated person and spread to other, unprotected individuals.
Now a new study led by researchers at UC San Francisco and Tel-Aviv University in Israel has revealed that in every vaccine-derived polio outbreak, the polio virus used the same three evolutionary steps to evolve from harmless vaccine into a regional menace. In the new study – published online March 23, 2017, in Cell – the researchers mapped out these key steps, identifying so-called “gatekeeper mutations” that must occur before the vaccine can evolve and regain full virulence. They have used this knowledge to develop a new polio vaccine that should be unable to escape and cause outbreaks, which they hope to put into clinical trials soon.
“If one could get everyone fully vaccinated, this would prevent the virus from being able to spread and evolve, but particularly in areas of the world that are riddled with conflict and poverty, it is very hard to get full coverage,” said Raul Andino, PhD, a professor of microbiology and immunology at UCSF and senior author of the new study. “Thus, it has been critical to understand how the virus manages to evolve virulence, and come up with strategies to stop it.”

Official Push to Hide Drug & Vaccine Side Effects; Reduce Informed Consent
Posted on: Monday, June 26th 2017 at 3:45 pm
Written By: Jefferey Jaxen
In a disturbing turn of events, Big Pharma pushes to hijack informed consent by removing side effects from direct-to-consumer pharmaceutical advertising.
Direct-to-consumer pharmaceutical advertising (DTCPA) has exploded during the past several decades and is now the most prominent type of health communication the public encounters. DTCPA has been legal in the US since 1985, but exponentially expanded in 1997 when the Food and Drug Administration (FDA) changed a rule that once forced drug companies to offer a detailed list of side-effects in their long format commercials. The impact was immediate. Spending by drug companies on TV ads hit $664 million within a year. By 2005, the industry was spending more than $3 billion annually on televised direct-to-consumer (DTC) ads. 2008 saw Big Pharma post just under $5 billion. Spending on DTCPA rose 9% to $5.6 billion in 2016 and expected to rise further in 2017. To date, the US and New Zealand are the only two countries that allow DTCPA.
In what appears to be a coordinated effort both the FDA and the UK’s Academy of Medical Sciences (AMS) have each announced their intentions to hide or eliminate side effects from DTCPA and patient information leaflets (PIL). Lending credence to larger picture unfolding, both the FDA and the AMS announced their intentions to toy with further concealing drug and vaccine side effects on the same day [June 19].
Hijacking Informed Consent
The FDA announced it will begin a study titled Experimental Study of Risk Information Amount and Location in Direct-to-Consumer Print Ads. To fulfill the regulatory requirements for fair balance and the brief summary (the part of the ad which lists side effects, contraindications and effectiveness) drug companies must included risk information about their product in DTC print ads both in the main part of the ad where the product claims appear, and in a separate brief summary page. The FDA’s rationale for its new study claims that listing the unfavorable risks and side effects of a drug may be ‘overwarning’ consumers in addition to potentially leading to habituation. The agency’s Office of Prescription Drug Promotion is planning to test what happens when the side effects are reduced or eliminated from DTC television ads.
The AMS is a self-proclaimed “independent body in the UK representing the diversity of medical science” who, according to their website, is funded by GlaxoSmithKline, Amgen, Merck Sharp and Dohme, and Roche. Their recent project was “…to examine how the generation, trustworthiness and communication of scientific evidence can be enhanced [key term] to strengthen its role in decisions by patients, carers, healthcare professionals and others about the benefits and harms of medicines.” In other words since the UK can’t market drugs and vaccines directly to the consumers the AMS has set out to see how eliminating informed consent by hiding product side effects from patients will boost pharmaceutical product uptake. Their report starts out with perhaps the most important statistic to date showing widespread rejection of Big Pharma and its influence on the medical community:
“Only about a third (37%) of the public trust evidence from medical research, compared to approximately two-thirds (65%) who trust the experiences of their friends and family, according to a report launched today.”
In a rational health world focused on true healing, such dismal percentages would be evidence to rework a broken medical system, remove Big Pharma conflicts of interest in research and medical practice and begin to listen to patients. Instead, the AMS report goes on to call for “improvements” to the PIL and “a bigger role” for UK’s National Health Service to be a “source of trusted information online”. The report calls for the European Commission and the European Medicines Agency (EMA) to work with pharmaceutical companies to “reform” PIL’s.
Currently the EMA has two open complaints against it by the Nordic Cochrane Centre over maladministration, conflict of interest, secrecy and unprofessionalism concerning the handling of HPV vaccine safety data, research and whistleblowers. What kind of improvements in the PIL are being suggested? The AMS is calling for a more “balanced view” because there is too much focus on the potential side effects of drugs and vaccines on the PIL’s and not enough on their benefits. The rationale for reworking the PIL is not rooted in reality. The broken peer-reviewed process and pharmaceutical industry influence on medical research has continually omitted both greater incidences and number side effects along with exaggeration of benefits.

The Toxicity of Aluminum Adjuvants There are NO clinically approved vaccine aluminium adjuvants
Professor Christopher Exley, world’s leading expert on aluminium.
“There are NO clinically approved vaccine aluminium adjuvants !!!”
The Toxicity of Aluminum Adjuvants

Documentary – The Age of Aluminium (Die Akte Aluminium)
The Age of Aluminium: Die Akte Aluminium. A film and documentary created by Bert Ehgartner (Full English version).

Top Doctors Reveal Vaccines Turn Our Immune System Against Us
Dec 1, 2016
The research is hard to ignore, vaccines can trigger autoimmunity with a laundry list of diseases to follow. With harmful and toxic metals as some vaccine ingredients, who is susceptible and which individuals are more at risk?
No one would accuse Yehuda Shoenfeld of being a quack. The Israeli clinician has spent more than three decades studying the human immune system and is at the pinnacle of his profession. You might say he is more foundation than fringe in his specialty; he wrote the textbooks. The Mosaic of Autoimmunity, Autoantibodies, Diagnostic Criteria in Autoimmune Diseases, Infection and Autoimmunity, Cancer and Autoimmunity – the list is 25 titles long and some of them are cornerstones of clinical practice. Hardly surprising that Shoenfeld has been called the “Godfather of Autoimmunology” – the study of the immune system turned on itself in a wide array of diseases from type 1 diabetes to ulcerative colitis and multiple sclerosis.
But something strange is happening in the world of immunology lately and a small evidence of it is that the Godfather of Autoimmunology is pointing to vaccines – specifically, some of their ingredients including the toxic metal aluminum – as a significant contributor to the growing global epidemic of autoimmune diseases. The bigger evidence is a huge body of research that’s poured in in the past 15 years, and particularly in the past five years. Take for example, a recent article published in the journal Pharmacological Research in which Shoenfeld and colleagues issue unprecedented guidelines naming four categories of people who are most at risk for vaccine-induced autoimmunity.
“On one hand,” vaccines prevent infections which can trigger autoimmunity, say the paper’s authors, Alessandra Soriano, of the Department of Clinical Medicine and Rheumatology at the Campus Bio-Medico University in Rome, Gideon Nesher, of the Hebrew University Medical School in Jerusalem and Shoenfeld, founder and head of the Zabludowicz Center of Autoimmune Diseases in the Sheba Medical Center at Tel Hashomer. He is also editor of three medical journals and author of more than 1,500 research papers across the spectrum of medical journalism and founder of the International Congress on Autoimmunology. “On the other hand, many reports that describe post-vaccination autoimmunity strongly suggest that vaccines can indeed trigger autoimmunity. Defined autoimmune diseases that may occur following vaccinations include arthritis, lupus (systemic lupus erythematosus, SLE) diabetes mellitus, thrombocytopenia, vasculitis, dermatomyosiositis, Guillain-Barre syndrome and demyelinating disorders. Almost all types of vaccines have been reported to be associated with the onset of ASIA.”
ASIA – or Autoimmune/inflammatory Syndrome Induced by Adjuvants (also known as Shoenfeld’s syndrome) — first appeared in the Journal of Autoimmunology four years ago. It is an umbrella term for a collection of similar symptoms, including Chronic Fatigue Syndrome, that result after
exposure to an adjuvant – an environmental agent including common vaccine ingredients that stimulate the immune system. Since then an enormous body of research, using ASIA as a paradigm, has begun to unravel the mystery of how environmental toxins, particularly the metal aluminum used in vaccines, can trigger an immune system chain reaction in susceptible individuals and may lead to overt autoimmune disease.

Study – ‘ASIA’ – autoimmune/inflammatory syndrome induced by adjuvants.
Abstract
The role of various environmental factors in the pathogenesis of immune mediated diseases is well established. Of which, factors entailing an immune adjuvant activity such as infectious agents, silicone, aluminium salts and others were associated with defined and non-defined immune mediated diseases both in animal models and in humans. In recent years, four conditions: siliconosis, the Gulf war syndrome (GWS), the macrophagic myofasciitis syndrome (MMF) and post-vaccination phenomena were linked with previous exposure to an adjuvant. Furthermore, these four diseases share a similar complex of signs and symptoms which further support a common denominator.Thus, we review herein the current data regarding the role of adjuvants in the pathogenesis of immune mediated diseases as well as the amassed data regarding each of these four conditions. Relating to the current knowledge we would like to suggest to include these comparable conditions under a common syndrome entitled ASIA, “Autoimmune (Auto-inflammatory) Syndrome Induced by Adjuvants”.

200 Evidence-Based Reasons NOT To Vaccinate – FREE Research PDF Download!
Posted on: Sunday, February 22nd 2015 at 1:45 pm
Written By: GreenMedInfo Research Group
This article is copyrighted by GreenMedInfo LLC, 2017
The media, your pediatrician, politicians and health authorities like the CDC and FDA claim that vaccines are safe and effective. So why do hundreds of peer-reviewed studies indicate the opposite is true? Read, download, and share this document widely to provide the necessary evidence-based counterbalance to the pro-vaccination propaganda that has globally infected popular consciousness and discussion like an intractable disease.
It is abundantly clear that if the present-day vaccine climate, namely, that everyone must comply with the CDC’s one-size-fits-all vaccination schedule or be labeled a health risk to society at large, is to succumb to open and balanced discussion, it is the peer-reviewed biomedical evidence itself that is going to pave the way towards making rational debate on the subject happen.
With this aim in mind, GreenMedInfo.com has painstakingly collected over 300 pages of study abstracts culled directly from the National Library of Medicine’s pubmed.gov bibliographic database on the wide-ranging adverse health effects linked to vaccines in the today’s schedule (over 200 distinct adverse effects, including death), as well as numerous studies related to vaccine contamination, and vaccine failure in highly vaccine compliant populations.
This is the literature that the media, politicians and governmental health organizations like the CDC, pretend with abject dishonesty does not exist – as if vaccine injury did not happen, despite the over 3 billion dollars our government has paid out to vaccine injured through the National Vaccine Injury Compensation Fund since it was inaugurated in 1986.
We have written extensively about this research previously, highlighting different studies, focusing on translating their implications to the lay persons (view our vaccine article section here), but we believe that collecting and condensing solely the primary literature itself makes a much more powerful statement.
This document is being made free to download to the world at large in order to encourage the lay public, health professionals, activists, and elected officials alike to read, acknowledge and share the voluminous literature with their family, friends, colleagues and related stakeholders. You will find this research undermines the national and global agenda to continue to expand the vaccine schedule (on behalf of a vaccine industry that is indemnified against lawsuit for defective or harmful products), with increasing legislative pressure to remove exemptions and mandate them against the evidence of harm and at best equivocal effectiveness as a preventive health measure.
If the vaccination arm of modern medicine today is to continue to promote itself as a science- and evidence-based practice, it must acknowledge and incorporate the implications of the research we are releasing here, or lose any pretense at credibility. Failing to do so will reveal that the widespread push to remove your choice in the matter is agenda and not evidence driven, and due to the fact that vaccines all carry the risk of irreversible harm and even death (any vaccine insert proves this), it clearly violates the Nuremberg code of medical ethics to promote them as a priori safe and effectiveness.
http://www.greenmedinfo.com/anti-therapeutic-action/vaccination-all
http://cdn.greenmedinfo.com/sites/default/files/gmipub_58635_anti_therapeutic_action_vaccination_all.pdf

Vaccine Mechanisms in Autism
Disclaimer: The Content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this Website. All research is referenced at the end of this article.
This article will explain how specific vaccine adjuvants, in combination with the herbicide glyphosate, keep the brain in a permanent inflammatory state leading to the symptoms as seen in autism. It will point out key adjuvants believed to be involved with the development of autism. Lastly, it will briefly touch upon the key part in the brain involved and touches upon novel therapeutic possibilities.