French scientists sound the alarm about aluminum in vaccines — crickets from media and health authorities
PARIS, France — Roman K. Gherardi and his colleagues from the Université Paris Est Créteil (“UPEC”)in France issued a worldwide warning in late 2016 about the aluminum adjuvant used in childhood vaccines. Their paper, published in the highly-respected journal Toxicology, is deeply distrubing for any parent contemplating vaccinating their child according to the present schedule recommended by the American Centers for Disease Control (“CDC”). And, it’s highly likely that this is the first time you’ve ever heard about it.It’s safe to say that this study’s conclusions have revolutionized our understanding of aluminum adjuvant, the kind used in most children’s vaccines.The French study authors were very concerned about the widespread use of aluminum adjuvant: “Concerns about its [aluminum adjuvant’s] safety emerged following recognition of its unexpectedly long-lasting biopersistence within immune cells in some individuals, and reports of chronic fatigue syndrome, cognitive dysfunction, myalgia, dysautonomia and autoimmune/inflammatory features temporally linked to multiple Al-containing vaccine administrations.”
Journal of Toxicology – 28 November 2016
Study – Non-linear dose-response of aluminium hydroxide adjuvant particles: Selective low dose neurotoxicity
Guillemette Crépeaux a , b , * , 2 , Housam Eidi a , c , Marie-Odile David c , Yasmine Baba-Amer a , Eleni Tzavara d , Bruno Giros d , François-Jérôme Authier a , Christopher Exley e , Christopher A. Shaw f , Josette Cadusseau a , g , 1 ,Romain K. Gherardi a,1
a Inserm U955 E10, Université Paris Est Créteil (UPEC), Créteil, France
b Ecole Nationale Vétérinaire d’Alfort,Maisons-Alfort,France
c Inserm U1204, Université Evry Val d’ Essonne (UEVE),Evry,France
d Inserm U1130, CNRS UMR 8246, UPMC UM CR18,Paris, France
e Birchall Centre, Keele University,Staffordshire,UK
f Department of Ophthalmology, University of British Columbia,Vancouver,BC,Canada
g Faculté des Sciences&TechnologiesUPEC,Créteil,France
Abstarct
Aluminium (Al) oxyhydroxide (Alhydrogel 1), the main adjuvant licensed for human and animal vaccines, consists of primary nanoparticles that spontaneously agglomerate. Concerns about its safety emerged following recognition of its unexpectedly long-lasting biopersistence within immune cells in some individuals, and reports of chronic fatigue syndrome, cognitive dysfunction, myalgia, dysautonomia and autoimmune/inflammatory features temporally linked to multiple Al-containing vaccine administrations. Mouse experiments have documented its capture and slow transportation by monocyte-lineage cells from the injected muscle to lymphoid organs and eventually the brain. The present study aimed at evaluating mouse brain function and Al concentration 180 days after injection of various doses of Alhydrogel 1 (200, 400 and 800 mg Al/kg of body weight) in the tibialis anterior muscle in adult female CD1 mice. Cognitive and motor performances were assessed by 8 validated tests, microglial activation by Iba-1 immunohistochemistry, and Al level by graphite furnace atomic absorption spectroscopy. An unusual neuro-toxicological pattern limited to a low dose of Alhydrogel 1 was observed. Neurobehavioural changes, including decreased activity levels and altered anxiety-like behaviour, were observed compared to controls in animals exposed to 200 mg Al/kg but not at 400 and 800 mg Al/kg. Consistently, microglial number appeared increased in the ventral forebrain of the 200 mg Al/kg group. Cerebral Al levels were selectively increased in animals exposed to the lowest dose, while muscle granulomas had almost completely disappeared at 6 months in these animals. We conclude that Alhydrogel 1 injected at low dose in mouse muscle may selectively induce long-term Al cerebral accumulation and neurotoxic effects. To explain this unexpected result, an avenue that could be explored in the future relates to the adjuvant size since the injected suspensions corresponding to the lowest dose, but not to the highest doses, exclusively contained small agglomerates in the bacteria-size range known to favour capture and, presumably, transportation by monocyte-lineage cells. In any event, the view that Alhydrogel 1 neurotoxicity obeys “ the dose makes the poison ” rule of classical chemical toxicity appears overly simplistic.
Study – Spontaneous Integration of Human DNA Fragments into Host GenomeK. Koyama, T. A. DeisherSound Choice Pharmaceutical Institute, Seattle, WA
Introduction A trio of recent publications in the journal NEURON reports the presence of hundreds of diverse de novo gene mutations indicating that autism spectrum disorder (ASD) may be a disease of genomic instability, with a significant environmental component. Altered double strand break formation and repair pathways (DSB) may be a commonality among the diverse genetic mutations that have been documented in ASD. US birth year change points in AD are apparent in 1980, 1988 and 1996, coinciding with the switch to or introduction of childhood vaccines contaminated with human endogenous retrovirus K (HERVK) and human fetal DNA fragments (6). We hypothesize that the HERVK and human fetal DNA contaminants could contribute to the genomic instability of ASD as demonstrated by de novo mutations. Cell free DNA can be taken up by healthy cells via receptor mediated uptake or may spontaneously penetrate cell membranes that have altered permeability, for instance, during inflammatory reactions. Nuclear uptake of cell free DNA fragments is thought to provide a source for maintenance of DNA integrity during rescue of collapsed replication forks or base lesion repair. Spontaneous extracellular DNA uptake has also been exploited for gene therapy as well as for cellular gene correction (2,4,5,7,8, and 9). While free DNA uptake has been used advantageously, the process has also been associated with generation of mutations and chromosomal aberrations (3). Vaccines manufactured using human fetal cells contain residual DNA fragments (50-500 bp) (Table I). It is possible that these contaminating fragments could be incorporated into a child’s genome and disrupt normal gene function, leading to autistic phenotypes. In this study we demonstrate foreign DNA uptake in human cells and genomic integration by incubating the cells with Cy3-labeled human Cot1 (placental) DNA fragments which represents contaminating residual human fetal DNA in vaccines
Conclusion
Not only damaged human cells, but also healthy human cells can take up foreign DNA spontaneously. Foreign human DNA taken up by human cells will be transported into nuclei and be integrated into host genome, which will cause phenotype change. Hence, residual human fetal DNA fragments in vaccine can be one of causes of autism spectrum disorder in children through vaccination. Vaccine must be safe without any human DNA contaminations or reactivated viruses, and must be produced in ethically approved manufacturing processes
Study – Abortive and subclinical poliomyelitis in a family during the 1992 epidemic in The Netherlands
AuthorsKroon FP1, Weiland HT, van Loon AM, van Furth R.
Author informationDepartment of Infectious Diseases, University Hospital Leiden, The Netherlands.
AbstractWe describe a case of abortive poliomyelitis due to poliovirus type 3 (PV3) in an unvaccinated woman and a subclinical poliovirus infection in her family during an epidemic in the Netherlands. The woman excreted the epidemic strain (PV3) for 7 weeks. Her two children received oral attenuated poliovirus vaccine and were subsequently found to excrete PV1 and PV2 vaccine strains in addition to the epidemic PV3 strain. Her husband, who had neutralizing antibodies to all three poliovirus types because of previous vaccination, initially excreted no virus; subsequently, however, the vaccine strain PV1 and the epidemic strain PV3 could be cultured from his feces. These observations demonstrate the ease with which poliovirus circulates among family members, including those with neutralizing antibodies.
1 Corinthians 15 Authorized (King James) Version (AKJV)
1 Moreover, brethren, I declare unto you the gospel which I preached unto you, which also ye have received, and wherein ye stand;
2 by which also ye are saved, if ye keep in memory what I preached unto you, unless ye have believed in vain.
3 For I delivered unto you first of all that which I also received, how that Christ died for our sins according to the scriptures;
4 and that he was buried, and that he rose again the third day according to the scriptures:
Hebrews 6 Authorized (King James) Version (AKJV)
1 Therefore leaving the principles of the doctrine of Christ, let us go on unto perfection; not laying again the foundation of repentance from dead works, and of faith toward God,
2 of the doctrine of baptisms, and of laying on of hands, and of resurrection of the dead, and of eternal judgment.
3 And this will we do, if God permit.
4 For it is impossible for those who were once enlightened, and have tasted of the heavenly gift, and were made partakers of the Holy Ghost,
5 and have tasted the good word of God, and the powers of the world to come,
6 if they shall fall away, to renew them again unto repentance; seeing they crucify to themselves the Son of God afresh, and put him to an open shame.
7 For the earth which drinketh in the rain that cometh oft upon it, and bringeth forth herbs meet for them by whom it is dressed, receiveth blessing from God:
8 but that which beareth thorns and briers is rejected, and is nigh unto cursing; whose end is to be burned.
1 Who hath believed our report? and to whom is the arm of the Lord revealed?
2 For he shall grow up before him as a tender plant,and as a root out of a dry ground:he hath no form nor comeliness;and when we shall see him,there is no beauty that we should desire him.
3 He is despised and rejected of men;a man of sorrows, and acquainted with grief:and we hid as it were our faces from him;he was despised, and we esteemed him not.
4 Surely he hath borne our griefs,and carried our sorrows:yet we did esteem him stricken,smitten of God, and afflicted.
5 But he was wounded for our transgressions,he was bruised for our iniquities:the chastisement of our peace was upon him;and with his stripes we are healed.
6 All we like sheep have gone astray;we have turned every one to his own way;and the Lord hath laid on him the iniquity of us all.
7 He was oppressed, and he was afflicted,yet he opened not his mouth:he is brought as a lamb to the slaughter,and as a sheep before her shearers is dumb,so he openeth not his mouth.
8 He was taken from prison and from judgment:and who shall declare his generation? for he was cut off out of the land of the living:for the transgression of my people was he stricken.
9 And he made his grave with the wicked,and with the rich in his death;because he had done no violence,neither was any deceit in his mouth.
10 Yet it pleased the Lord to bruise him;he hath put him to grief:when thou shalt make his soul an offering for sin,he shall see his seed, he shall prolong his days,and the pleasure of the Lord shall prosper in his hand.
11 He shall see of the travail of his soul, and shall be satisfied:by his knowledge shall my righteous servant justify many;for he shall bear their iniquities.
12 Therefore will I divide him a portion with the great,and he shall divide the spoil with the strong;because he hath poured out his soul unto death:and he was numbered with the transgressors;and he bare the sin of many,and made intercession for the transgressors.
a The Birchall Centre, Lennard-Jones Laboratories, Keele University, Staffordshire, ST5 5BG, United Kingdom
b Life Sciences, Keele University, Staffordshire, ST5 5BG, United Kingdom
c Department of Clinical Neuropathology, Kings College Hospital, London, SE5 9RS, United Kingdom
Abstract
Autism spectrum disorder is a neurodevelopmental disorder of unknown aetiology. It is suggested to involve both genetic susceptibility and environmental factors including in the latter environmental toxins. Human exposure to the environmental toxin aluminium has been linked, if tentatively, to autism spectrum disorder. Herein we have used transversely heated graphite furnace atomic absorption spectrometry to measure, for the first time, the aluminium content of brain tissue from donors with a diagnosis of autism. We have also used an aluminium-selective fluor to identify aluminium in brain tissue using fluorescence microscopy. The aluminium content of brain tissue in autism was consistently high. The mean (standard deviation) aluminium content across all 5 individuals for each lobe were 3.82(5.42), 2.30(2.00), 2.79(4.05) and 3.82(5.17) μg/g dry wt. for the occipital, frontal, temporal and parietal lobes respectively. These are some of the highest values for aluminium in human brain tissue yet recorded and one has to question why, for example, the aluminium content of the occipital lobe of a 15 year old boy would be 8.74 (11.59) μg/g dry wt.? Aluminium-selective fluorescence microscopy was used to identify aluminium in brain tissue in 10 donors. While aluminium was imaged associated with neurones it appeared to be present intracellularly in microglia-like cells and other inflammatory non-neuronal cells in the meninges, vasculature, grey and white matter. The pre-eminence of intracellular aluminium associated with non-neuronal cells was a standout observation in autism brain tissue and may offer clues as to both the origin of the brain aluminium as well as a putative role in autism spectrum disorder.
US National Library of Medicine
National Institutes of Health – Oct 2012
Goldman GS, Miller NZ.
Author information
Computer Scientist, Pearblossom, CA 93553, USA. gsgoldman@roadrunner.com
Abstract
In this study, the Vaccine Adverse Event Reporting System (VAERS) database, 1990-2010, was investigated; cases that specified either hospitalization or death were identified among 38,801 reports of infants. Based on the types of vaccines reported, the actual number of vaccine doses administered, from 1 to 8, was summed for each case. Linear regression analysis of hospitalization rates as a function of (a) the number of reported vaccine doses and (b) patient age yielded a linear relationship with r(2) = 0.91 and r(2) = 0.95, respectively. The hospitalization rate increased linearly from 11.0% (107 of 969) for 2 doses to 23.5% (661 of 2817) for 8 doses and decreased linearly from 20.1% (154 of 765) for children aged <0.1 year to 10.7% (86 of 801) for children aged 0.9 year. The rate ratio (RR) of the mortality rate for 5-8 vaccine doses to 1-4 vaccine doses is 1.5 (95% confidence interval (CI), 1.4-1.7), indicating a statistically significant increase from 3.6% (95% CI, 3.2-3.9%) deaths associated with 1-4 vaccine doses to 5.5% (95% CI, 5.2-5.7%) associated with 5-8 vaccine doses. The male-to-female mortality RR was 1.4 (95% CI, 1.3-1.5). Our findings show a positive correlation between the number of vaccine doses administered and the percentage of hospitalizations and deaths. Since vaccines are given to millions of infants annually, it is imperative that health authorities have scientific data from synergistic toxicity studies on all combinations of vaccines that infants might receive. Finding ways to increase vaccine safety should be the highest priority.
The Association of American Physicians and Surgeons notes that, because of public concerns that mercury (as thimerosal) in childhood vaccines might be contributing to soaring rates of autism, this component was mostly phased out as a “precaution.” Autism rates continued to rise, prompting authorities to assert that autism is not linked to mercury in vaccines and that vaccination policies are safe and appropriate, writes Neil Z. Miller in the winter issue of the Journal of American Physicians and Surgeons.
ABSTRACT
Aluminum is a neurotoxin, yet infants and young children are repeatedly injected with aluminum adjuvants from multiple vaccines during critical periods of brain development. Numerous studies provide credible evidence that aluminum adversely affects important biological functions and may contribute to neurodegenerative and autoimmune disorders. It is impossible to predetermine which vaccinated babies will succumb to aluminum poisoning. Aluminum-free health options are needed.
PDF: http://www.jpands.org/vol21no4/miller.pdf
Study Shows Evidence of Inflammatory Cells Loaded with Aluminum Crossing the Blood-Brain Barrier and Meningeal Membranes
(November 27, 2017) Staffordshire, UK — A new study published in the Journal of Trace Elements in Medicine and Biology provides the strongest indication yet that aluminum is an etiological agent in autism spectrum disorder (ASD), according to researchers at Keele University in England.
The study used transversely heated graphite furnace atomic absorption spectrometry to measure, for the first time, the aluminum content of brain tissue from five donors who had died with diagnoses of ASD. The results showed the donors to have had some of the highest values of aluminum yet measured in human brain tissue.
The mean (standard deviation) aluminum content across all five individuals for each lobe were 3.82(5.42), 2.30(2.00), 2.79(4.05) and 3.82(5.17) mg/g dry wt. for the occipital, frontal, temporal and parietal lobes respectively. Previous measurements of 60 brains from humans not diagnosed with ASD showed an average content of 1 mg/g dry wt. of brain tissue.
“One has to wonder why aluminum in the occipital lobe of a 15-year-old boy with autism would be a value that is at least 10 times higher than what might be considered acceptable for an elderly adult?” said Christopher Exley PhD, Professor in Bioinorganic Chemistry and author of the study. Another ground-breaking study by Exley and his team, published earlier in the year, identified similarly high levels of aluminum in the brains of individuals who died of familial Alzheimer’s disease.
When it comes to the most widely used adjuvant ingredient found within vaccines, aluminum, many questions have yet to be answered, particularly when it comes to where the aluminum goes after injection, an issue known as biopersistence.
One reason this question arises is because a causative role has been established in what’s known as macrophagic myofasciitis (MMF) lesion in patients who have myalgic encephalomyelitis, or brain inflammation. Myalgia, arthralgia, chronic fatigue, cognitive dysfunction, dysautonomia, and autoimmunity have been temporally linked to aluminium adjuvant-containing vaccine administration (Gherardi and Authier, 2003; Authier et al., 2003; Exley et al., 2009; Rosenblum et al., 2011; Santiago et al., 2014; Brinth et al., 2015; Palmieri et al., 2016).
“Evidence that aluminum-coated particles phagocytozed in the injected muscle and its draining lymph nodes can disseminate within phagocytes throughout the body and slowly accumulate in the brain further suggested that alum safety should be evaluated in the long term.”
US National Library of Medicine
National Institutes of Health – Jun 2015
Eidi H – 1,2, David MO – 3, Crépeaux G – 4, Henry L – 5, Joshi V – 6, Berger MH – 7, Sennour M – 8, Cadusseau J – 9,10, Gherardi RK – 11, Curmi PA – 12.
Author information
1 Institut National de la Santé et de la Recherche Médicale (INSERM) – UMR 1204, Université Evry-Val d’Essonne, Laboratoire Structure-Activité des Biomolécules Normales et Pathologiques, Evry, France. housam.eidi@gmail.com.
2 Inserm – U955, Université Paris Est, Faculté de Médecine, Créteil, France. housam.eidi@gmail.com.
3 Institut National de la Santé et de la Recherche Médicale (INSERM) – UMR 1204, Université Evry-Val d’Essonne, Laboratoire Structure-Activité des Biomolécules Normales et Pathologiques, Evry, France. MO.David@iut.univ-evry.fr.
4 Inserm – U955, Université Paris Est, Faculté de Médecine, Créteil, France. guillemette.crepeaux@gmail.com.
5 Institut National de la Santé et de la Recherche Médicale (INSERM) – UMR 1204, Université Evry-Val d’Essonne, Laboratoire Structure-Activité des Biomolécules Normales et Pathologiques, Evry, France. laetitia.henry@wanadoo.fr.
6 Institut National de la Santé et de la Recherche Médicale (INSERM) – UMR 1204, Université Evry-Val d’Essonne, Laboratoire Structure-Activité des Biomolécules Normales et Pathologiques, Evry, France. vandana.joshi@univ-evry.fr.
7 Laboratoire Pierre-Marie Fourt, Centre des Matériaux de l’Ecole des Mines de Paris and CNRS UMR 7633, Evry, France. marie-helene.berger@mines-paristech.fr.
8 Laboratoire Pierre-Marie Fourt, Centre des Matériaux de l’Ecole des Mines de Paris and CNRS UMR 7633, Evry, France. mohamed.sennour@ensmp.fr.
9 Inserm – U955, Université Paris Est, Faculté de Médecine, Créteil, France. josette.cadusseau@inserm.fr.
10 Faculté des Sciences et Technologie UPEC, Créteil, France. josette.cadusseau@inserm.fr.
11 Inserm – U955, Université Paris Est, Faculté de Médecine, Créteil, France. romain.gherardi@hmn.aphp.fr.
12 Institut National de la Santé et de la Recherche Médicale (INSERM) – UMR 1204, Université Evry-Val d’Essonne, Laboratoire Structure-Activité des Biomolécules Normales et Pathologiques, Evry, France. pcurmi@univ-evry.fr.
Abstract
BACKGROUND:
Aluminum oxyhydroxide (alum) is a crystalline compound widely used as an immunologic adjuvant of vaccines. Concerns linked to alum particles have emerged following recognition of their causative role in the so-called macrophagic myofasciitis (MMF) lesion in patients with myalgic encephalomyelitis, revealing an unexpectedly long-lasting biopersistence of alum within immune cells and a fundamental misconception of its biodisposition. Evidence that aluminum-coated particles phagocytozed in the injected muscle and its draining lymph nodes can disseminate within phagocytes throughout the body and slowly accumulate in the brain further suggested that alum safety should be evaluated in the long term. However, lack of specific staining makes difficult the assessment of low quantities of bona fide alum adjuvant particles in tissues.
METHODS:
We explored the feasibility of using fluorescent functionalized nanodiamonds (mfNDs) as a permanent label of alum (Alhydrogel(®)). mfNDs have a specific and perfectly photostable fluorescence based on the presence within the diamond lattice of nitrogen-vacancy centers (NV centers). As the NV center does not bleach, it allows the microspectrometric detection of mfNDs at very low levels and in the long-term. We thus developed fluorescent nanodiamonds functionalized by hyperbranched polyglycerol (mfNDs) allowing good coupling and stability of alum:mfNDs (AluDia) complexes. Specificities of AluDia complexes were comparable to the whole reference vaccine (anti-hepatitis B vaccine) in terms of particle size and zeta potential.
RESULTS:
In vivo, AluDia injection was followed by prompt phagocytosis and AluDia particles remained easily detectable by the specific signal of the fND particles in the injected muscle, draining lymph nodes, spleen, liver and brain. In vitro, mfNDs had low toxicity on THP-1 cells and AluDia showed cell toxicity similar to alum alone. Expectedly, AluDia elicited autophagy, and allowed highly specific detection of small amounts of alum in autophagosomes.
CONCLUSIONS:
The fluorescent nanodiamond technology is able to overcome the limitations of previously used organic fluorophores, thus appearing as a choice methodology for studying distribution, persistence and long-term neurotoxicity of alum adjuvants and beyond of other types of nanoparticles.
1 Corinthians 15 Authorized (King James) Version (AKJV)
1 Moreover, brethren, I declare unto you the gospel which I preached unto you, which also ye have received, and wherein ye stand;
2 by which also ye are saved, if ye keep in memory what I preached unto you, unless ye have believed in vain.
3 For I delivered unto you first of all that which I also received, how that Christ died for our sins according to the scriptures;
4 and that he was buried, and that he rose again the third day according to the scriptures:
Hebrews 6 Authorized (King James) Version (AKJV)
1 Therefore leaving the principles of the doctrine of Christ, let us go on unto perfection; not laying again the foundation of repentance from dead works, and of faith toward God,
2 of the doctrine of baptisms, and of laying on of hands, and of resurrection of the dead, and of eternal judgment.
3 And this will we do, if God permit.
4 For it is impossible for those who were once enlightened, and have tasted of the heavenly gift, and were made partakers of the Holy Ghost,
5 and have tasted the good word of God, and the powers of the world to come,
6 if they shall fall away, to renew them again unto repentance; seeing they crucify to themselves the Son of God afresh, and put him to an open shame.
7 For the earth which drinketh in the rain that cometh oft upon it, and bringeth forth herbs meet for them by whom it is dressed, receiveth blessing from God:
8 but that which beareth thorns and briers is rejected, and is nigh unto cursing; whose end is to be burned.
1 Who hath believed our report? and to whom is the arm of the Lord revealed?
2 For he shall grow up before him as a tender plant,and as a root out of a dry ground:he hath no form nor comeliness;and when we shall see him,there is no beauty that we should desire him.
3 He is despised and rejected of men;a man of sorrows, and acquainted with grief:and we hid as it were our faces from him;he was despised, and we esteemed him not.
4 Surely he hath borne our griefs,and carried our sorrows:yet we did esteem him stricken,smitten of God, and afflicted.
5 But he was wounded for our transgressions,he was bruised for our iniquities:the chastisement of our peace was upon him;and with his stripes we are healed.
6 All we like sheep have gone astray;we have turned every one to his own way;and the Lord hath laid on him the iniquity of us all.
7 He was oppressed, and he was afflicted,yet he opened not his mouth:he is brought as a lamb to the slaughter,and as a sheep before her shearers is dumb,so he openeth not his mouth.
8 He was taken from prison and from judgment:and who shall declare his generation? for he was cut off out of the land of the living:for the transgression of my people was he stricken.
9 And he made his grave with the wicked,and with the rich in his death;because he had done no violence,neither was any deceit in his mouth.
10 Yet it pleased the Lord to bruise him;he hath put him to grief:when thou shalt make his soul an offering for sin,he shall see his seed, he shall prolong his days,and the pleasure of the Lord shall prosper in his hand.
11 He shall see of the travail of his soul, and shall be satisfied:by his knowledge shall my righteous servant justify many;for he shall bear their iniquities.
12 Therefore will I divide him a portion with the great,and he shall divide the spoil with the strong;because he hath poured out his soul unto death:and he was numbered with the transgressors;and he bare the sin of many,and made intercession for the transgressors.
To my friends in Australia: the vaccine war deepens
The string of abuses laid on citizens of Australia by their government grows almost week by week.
Now, parental rights to raise children, without interference from the State, is under a new form of attack. This must be resisted.
Schools are bringing doctors on board, as a permanent feature. Young children will be subjected to medical diagnoses and treatment, without consent or approval from parents, even if those parents actively object. The State is stealing the role of guardian.
The Herald Sun reports. Read carefully:
“DOCTORS will have the power to treat students as young as 12 in schools even if parents refuse their consent.”
“GPs will consult at 100 Victoria high schools for up to one day a week as part of a $43.8 million program.”
“Guidelines released on Thursday show that even if a parent ‘expressly states’ that a doctor should not [examine] their child, the GP can if they deem the teen mature enough.”
“’Any student who wants to see the GP will be permitted to make an appointment,’ the policy said.”
“The GP will decide if the young person is mature enough to provide consent to any medical treatment for the prevailing issue.”
A young child “giving consent?” This is supposed to be “informed consent” when facing off with an adult doctor?
The handwriting is on the wall. Multiple vaccines will be given, to “bring children up to State standards.” This whole operation is, in fact, a front for forced vaccination. That’s the goal.
Vaccines for preventing influenza in healthy children
Authors’ conclusions
Influenza vaccines are efficacious in preventing cases of influenza in children older than two years of age, but little evidence is available for children younger than two years of age. There was a difference between vaccine efficacy and effectiveness, partly due to differing datasets, settings and viral circulation patterns. No safety comparisons could be carried out, emphasising the need for standardisation of methods and presentation of vaccine safety data in future studies. In specific cases, influenza vaccines were associated with serious harms such as narcolepsy and febrile convulsions. It was surprising to find only one study of inactivated vaccine in children under two years, given current recommendations to vaccinate healthy children from six months of age in the USA, Canada, parts of Europe and Australia. If immunisation in children is to be recommended as a public health policy, large-scale studies assessing important outcomes, and directly comparing vaccine types are urgently required. The degree of scrutiny needed to identify all global cases of potential harms is beyond the resources of this review.
This review includes trials funded by industry. An earlier systematic review of 274 influenza vaccine studies published up to 2007 found industry-funded studies were published in more prestigious journals and cited more than other studies independently from methodological quality and size. Studies funded from public sources were significantly less likely to report conclusions favourable to the vaccines. The review showed that reliable evidence on influenza vaccines is thin but there is evidence of widespread manipulation of conclusions and spurious notoriety of the studies. The content and conclusions of this review should be interpreted in the light of this finding.
Through my extensive research and my work throughout the years, I have discovered that vaccinations are causing impaired blood flow (ischemia) to brain and body from clinically silent to death. These are strokes – across the board for all of us. I have reason to believe that all are being affected and all vaccinations ARE causing the overwhelming rise in autism, specific learning disabilities, attention deficit disorders, sudden infant death, gulf war syndrome, dementia, seizure disorders, some cancers it would appear, and much much more.
American Schools Faltering Under the Weight of Mental Health Issues in Kids
By Anne Dachel
While so many parents have been diligently trying to get the message across to the world that injecting known toxins into babies and pregnant women is destroying children everywhere, the perpetrators of this crime against humanity have come up with their own version of reality.
The latest really big lie about the damage done to our kids
For the last several months I’ve been compiling stories about the disaster zones our schools are becoming. Out-of-control behavior now routinely seen in students is being dealt with desperate measures. Physical restraints and seclusion rooms are part of the typical school environment. “Behavior coaches” and off-duty police are regular members of the staff in elementary schools. “Sensory rooms” where students can calm down are an accepted part of schools. Special ed is not just about learning disabilities but also about “mental health problems.” Schools are linking up with local mental health agencies to try and address student behavior. Sped students are being excluded from schools across Britain and Ireland in soaring numbers, even down to pre-school aged children, because of behavior.
The evidence that something is horribly wrong with today’s children is worldwide and it’s growing. U.S. Health officials have been silent on these issues, but I see a change happening. Actually, it’s been several years in the making, but it’s just now in the news everywhere in our country.
WHY ARE OUR KIDS SO DYSFUNCTIONAL? SIMPLE: They’ve experienced CHILDHOOD TRAUMA at the hands of their parents.
Aluminium dans les vaccins : le rapport qui dérange
Florence Méréo – 21 septembre 2017
Dans un rapport jamais rendu public depuis mars, des scientifiques pointent les risques induits par la présence d’aluminium dans les vaccins.
On y lit des échanges cordiaux mais surtout un débat âpre et passionné. Ces documents que nous nous sommes procurés, c’est l’avis du conseil scientifique de l’ANSM, le gendarme du médicament, et l’ensemble des discussions que les spécialistes ont mené sur l’étude de l’équipe du professeur Gherardi, chef du service neuromusculaire à l’hôpital Henri Mondor de Créteil, évaluant la neurotoxicité de l’aluminium présent dans les vaccins.
Hepatitis B Vaccine Discontinued After Three Newborn Babies Die
Families of three babies who died shortly after receiving their routine hepatitis B vaccine are mourning the loss of their children. The babies, vaccinated in Vietnam under the country’s National Expanded Program on Immunization, died on July 20 in the central province of Quang Tri, according to the report. [1]
The Vietnamese Health Department has since opted to discontinue the use of two vaccine lots in the entire country to protect other babies from a similar, tragic fate. According to officials, the vaccines were not expired and were properly stored. They were administered by a nurse with over twenty years of experience. [2]
On July 21, the nation’s health minister, Nguyen Thi Kim Tien, sent her condolences to the families of the deceased infants, ordering vaccine experts to investigate the tragedy. Preliminary investigations have identified anaphylactic shock as the cause of death. The chairperson of the vaccine program has asked parents to “keep calm” and continue vaccinating their children.
Health representatives have conducted damage control with home visits to the grieving parents, paying each family $377 and offering free medical care to the mothers at the hospital where their babies received the deadly vaccinations.
Vaccini e le linee cellulari di feti abortiti. Attacco alla genetica umana?
Facebook.com – luglio 2017 Marcello Pamio – Vaccini e salute
Sugli effetti collaterali dei «farmaci pediatrici» chiamati vaccini non ci sono dubbi se non nei cervelli di quelle persone profondamente analfabete e ignoranti che si informano tramite la televisione e i giornali, e da parte di quel mondo scientifico e corrotto collegato a doppia mandata con le lobbies della chimica e farmaceutica.
Moltissimi autori, ricercatori e medici onesti intellettualmente descrivono che la causa degli effetti avversi starebbe non tanto nella parte antigenica (virale o batterica che sia), quanto negli adiuvanti e conservanti usati dalle industrie: sostanze neurotossiche (sali di alluminio e mercurio, ecc.), cancerogene (formaldeide, ecc.), antibiotici, ecc.
Tutto estremamente corretto. Ma forse c’è dell’altro…
I vaccini contengono sostanze molto meno note – perché coperte dall’inviolabile segreto industriale – che si nascondono dietro sigle e/o acronimi e che potrebbero giocare invece un ruolo prioritario nell’eziologia di gravissime e incurabili patologie, per non parlare dell’inquietante modifica della genetica umana…
Le sostanze in questione sono: MRC-5, WI-38 e Vero.
Ecco le informazioni riportate dai bugiardini delle rispettive società produttrici.
VACCINO INFANRIX HEXA
Nel vaccino esavalente prodotto dalla Glaxo contro difterite, tetano, epatite-B, poliomielite, pertosse e haemophilus influenzae tipo B:
«prodotto da cellule di lievito (S. cerevisiae) tramite tecnologia del DNA ricombinante»;
«propagato in cellule VERO».
VACCINO M-M-R VAXPRO
Nel vaccino trivalente prodotto dalla Sanofi Pasteur contro morbillo, parotite, rosolia:
«prodotto su cellule embrionali di pollo»;
«prodotto su fibroblasti di polmone diploidi umani WI-38».
VACCINO PRIORIX
Nel vaccino quadrivalente prodotto dalla Glaxo contro morbillo, parotite, rosolia, varicella:
«coltivato in colture di cellule embrionali di pollo»;
«coltivato in cellule diploidi umani MRC-5».
VACCINO PROQUAD
Nel vaccino quadrivalente della Sanofi Pasteur contro morbillo, parotite, rosolia, varicella:
«prodotto su cellule embrionali di pollo»;
«prodotto su fibroblasti di polmone diploidi umani WI-38»;
«prodotto su cellule diploidi umani MRC-5».
VACCINO PENTAVAC
Nel vaccino pentavalente prodotto dalla Sanofi Pasteur contro difterite, tetano, pertosse, polio, haemophilus influenzae tipo B:
«adsorbito su alluminio idrossido»;
«prodotto su cellule VERO».
Per far crescere i ceppi virali usati poi nei vaccini, le corporation necessitano di un terreno di coltura rappresentato da cellule umane o animali o entrambe assieme (pollo e uomo).
Vediamo adesso nel dettaglio cosa rappresentano e soprattutto cosa nascondono le sigle:
VERO, WI-38, MRC-5.
10 Reasons Why Flu Shots Are More Dangerous Than a Flu!
Before we get into the very sensitive topic presented here, let us be very clear that we’re not against vaccination. We practice critical thought and this isn’t a black or white issue. There are times when vaccination it’s absolutely necessary. This my friends isn’t one of those times.
What we are against is blind acceptance of using a compound that isn’t proven safe when there are MANY natural alternatives to boost your immune system. We are talking about the flu here not small pox.
Make no mistake, when it comes to the flu, it’s a money driven game!
The verdict is out on flu shots. Many medical experts now agree it is more important to protect yourself and your family from the flu vaccine than the flu itself. Let’s take a look at the reasons behind this verdict
Please Create the RFK Independent Vaccine Safety Commission
In January, you approached Robert Kennedy Jr. to head up an independent commission investigating vaccine safety. We respectfully request that you follow through on this sensible plan and create a truly independent commission with no ties to the CDC or pharmaceutical industry to take another look at vaccine safety.
The rates of developmental disabilities in the United States are skyrocketing – 1 in 6 children, 1 in 4 boys. 1 in 20 boys will receive an autism diagnosis, up from 1 in 10,000 in the 1970s. Clearly something is wrong and the smoking gun points to vaccines. If you want to Make America Great Again you have to Make America’s Children Great – and this requires ending the life-long harm caused by an excessive and unsafe vaccine schedule. We currently have the sickest generation of American children in the history of this country and amongst the highest rates of Sudden Infant Death Syndrome in the industrialized world.
An interview with Robert Kennedy Jr. on vaccines
By Helen Branswell
In the early days of 2017, proponents of vaccination were deeply concerned. Donald Trump, who has long espoused a debunked link between vaccines and autism, was set to enter the White House. He met with environmental activist Robert Kennedy Jr., who has for years argued that vaccines can cause a range of developmental and other health conditions. Kennedy emerged to report he’d been asked to chair a commission into vaccine safety.
But seven months later, no such commission has been appointed and the crisis-mired White House has declined to say whether the plan has been shelved.
STAT contacted Kennedy to see where plans stood. He would only speak on condition that STAT publish the interview in a Q&A format. He argued that his assertions — which are disputed as a misreading of the scientific literature by many mainstream scientists — have been misquoted and misrepresented in the media.
Here is STAT’s conversation with Kennedy. It has been lightly edited, for length and readability.
The question I want to ask you relates to the vaccine safety commission that you had announced in January that you were going to head, after you met with then President-elect Trump. It’s been a number of months now, and there hasn’t been any further public announcement. And so we’ve been wondering: Where does this stand?
I’ve had no discussions specifically about the vaccine safety commission, probably since February. I’ve spoken to the White House about other issues of vaccine safety and had a number of follow-up meetings.
Study – The putative role of environmental aluminium in the development of chronic neuropathology in adults and children. How strong is the evidence and what could be the mechanisms involved?
Abstract
The conceptualisation of autistic spectrum disorder and Alzheimer’s disease has undergone something of a paradigm shift in recent years and rather than being viewed as single illnesses with a unitary pathogenesis and pathophysiology they are increasingly considered to be heterogeneous syndromes with a complex multifactorial aetiopathogenesis, involving a highly complex and diverse combination of genetic, epigenetic and environmental factors. One such environmental factor implicated as a potential cause in both syndromes is aluminium, as an element or as part of a salt, received, for example, in oral form or as an adjuvant. Such administration has the potential to induce pathology via several routes such as provoking dysfunction and/or activation of glial cells which play an indispensable role in the regulation of central nervous system homeostasis and neurodevelopment. Other routes include the generation of oxidative stress, depletion of reduced glutathione, direct and indirect reductions in mitochondrial performance and integrity, and increasing the production of proinflammatory cytokines in both the brain and peripherally. The mechanisms whereby environmental aluminium could contribute to the development of the highly specific pattern of neuropathology seen in Alzheimer’s disease are described. Also detailed are several mechanisms whereby significant quantities of aluminium introduced via immunisation could produce chronic neuropathology in genetically susceptible children. Accordingly, it is recommended that the use of aluminium salts in immunisations should be discontinued and that adults should take steps to minimise their exposure to environmental aluminium.
Australia Bans Truth-Telling Mother From Country For Three Years…And It Backfired
The date was August 8th and the Vaxxed team had just wrapped up a two-week tour of Australia, where the communities of parents received their info with great interest. It was time for the team, consisting of a medical doctor, a scientist, a videographer, and a mother of a vaccine-injured son to pass through Australia’s Department of Immigration within the airport on the way to their flight to New Zealand. Three passed through unhassled, one didn’t. Vaxxed team member Polly Tommey describes what happened to her:
“I get taken to one side and that’s when two immigration police take me into a room and tell me that I’ve been detained and ask for my phone…and then they told me that I was in violation of my Visa and they took my phone and went right through everything in my phone. They typed in ‘Australia’ they went through every contact and every email that there had been with myself and the team. They took my phone away and photographed everything.”
In an instant Tommey was a persecuted individual who moments later would find out she was officially banned from Australia for three years. Next, it came time for airport security immigration officers to address one of the reasons Tommey was being harassed:
“Then they asked me about Vaxxed. Did I have a copy of it? Endless questions about Vaxxed being a very dangerous film with lies…I’m a mother recording stories from parents. And parents come to me to tell their stories. I didn’t seek them out, they come to me. And that is more of a threat than anything else?”
How did we get to the point where a mother can be banned from a western country for simply offering a voice to families?
The Wild Doc – What Officials Can Do To End Unnecessary Drug Overdoses/ Vaccine Awareness Month Brings New Confirmation That Vaccines Are Causing SIDS.
Relevant to the back-end profits (and back-end injuries) industry is generating from the autism epidemic. Abilify is in the class of second generation antipsychotics frequently pushed on individuals with autism by mainstream doctors as part of the $5 billion (and rising) “autism drug” market.
Dr.Russell Blaylock Exposes The Gardasil, HPV Vaccine Fraud
A shocking interview by Mike Adams (The health ranger) with Dr. Russell Blaylock who exposes to total criminal fraud of HPV vaccines and the vaccine industry.
Hear Why He Calls The HPV Vaccine a Crime Against Kids!
The HPV vaccine continues to be a hotly debated issue. Robert Scott Bell, popular radio host and homeopathic practitioner, discusses the theory behind the HPV vaccine and whether or not he thinks it’s safe. http://www.ihealthtube.com
The Health Ranger – Gardasil HPV Vaccine Hoax Exposed
This video exposes the truth about Gardasil and HPV vaccinations: They don’t work and may actually be dangerous to women. The FDA knew HPV did not cause cervical cancer in 2003.
HPV Gardasil Vaccine Proves Lethal – 236 Girls have now Died
236 Girls have now died in America – http://sanevax.org/
Irish Times 8.1.2012-Schoolgirl vaccine uptake of 82% beats target figures http://j.mp/zuYds8
236 girls have now died in America and the rest of the World, But the Irish Times keeps this quite, Irish Dr Kevin Kelleher, assistant national director of health protection at the HSE, welcomed the high uptake on Gardisil Vaccinations, he fails to give the facts also, says its excellent!
The 82 per cent uptake was “excellent” and was equal to or greater than those achieved in the first year of programmes in other countries such as the United Kingdom and Australia. He said the figures were great credit to the vaccination teams.
MMR gave our boy organ failure and then loss of legs #vaxxed #truth #science #Praybig
Why My Wife and I Decided Not To Vaccinate Our Daughter
Author: Jason Christoff
When my wife was pregnant we knew the vaccine issue was coming our way and we put it off as long as possible. As the day fast approached, I started to investigate and compile some information for my wife because she trusted that I would make sure she understood what the main issues were regarding vaccination. We had heard vaccinations were potentially dangerous but we didn’t know if that applied to all children or just some. We weren’t aware if vaccination was beneficial for some babies and maybe not for others. We were new to being parents and we didn’t want to make any mistakes. We certainly didn’t want our baby getting sick if we could do something about it proactively. We wanted our baby to have the most comfortable journey through life possible and if that meant giving our new born vaccines, so she could avoid disease now and in the future, then that’s what we were going to do. After researching for a couple of days, we were more than shocked at what we were uncovering.
Study – Neurological and autoimmune disorders after vaccination against pandemic influenza A (H1N1) with a monovalent adjuvanted vaccine: population based cohort study in Stockholm, Sweden.
RESULTS:
Excess risks among vaccinated compared with unvaccinated people were of low magnitude for Bell’s palsy (hazard ratio 1.25, 95% confidence interval 1.06 to 1.48) and paraesthesia (1.11, 1.00 to 1.23) after adjustment for age, sex, socioeconomic status, and healthcare utilisation. Risks for Guillain-Barré syndrome, multiple sclerosis, type 1 diabetes, and rheumatoid arthritis remained unchanged. The risks of paraesthesia and inflammatory bowel disease among those vaccinated in the early phase (within 45 days from 1 October 2009) of the vaccination campaign were significantly increased; the risk being increased within the first six weeks after vaccination. Those vaccinated in the early phase were at a slightly reduced risk of death than those who were unvaccinated (0.94, 0.91 to 0.98), whereas those vaccinated in the late phase had an overall reduced mortality (0.68, 0.64 to 0.71). These associations could be real or explained, partly or entirely, by residual confounding.
CONCLUSIONS:
Results for the safety of Pandemrix over 8-10 months of follow-up were reassuring -notably, no change in the risk for Guillain-Barré syndrome, multiple sclerosis, type 1 diabetes, or rheumatoid arthritis. Relative risks were significantly increased for Bell’s palsy, paraesthesia, and inflammatory bowel disease after vaccination, predominantly in the early phase of the vaccination campaign. Small numbers of children and adolescents with narcolepsy precluded any meaningful conclusions.
Injecting Aluminum Official Trailer
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In the early 90s, a mysterious muscular disease with symptoms that included severe muscle and joint pain began to surface among multiple patients in France. In 1993, a team of doctors in Paris discovered that these patients had developed a new disease called Macrophagic Myofascitis, or MMF, which occurs when the aluminum hydroxide adjuvant from a vaccine remains embedded in the muscle tissue and causes an immune reaction. Featuring interviews with patients, doctors, scientists, and influential politicians, Injecting Aluminum calls in to question the public health policies around aluminum in vaccines and examines aluminum’s devastating effects on the human body.
IMPFEN MUSS FREIWILLIG BLEIBEN!
In vielen Ländern Europas dürfen Eltern schon jetzt nicht mehr frei entscheiden, ob, wann und wogegen ihre Kinder geimpft werden. Auch in Deutschland werden die Daumenschrauben angezogen, aktuell wird diskutiert, man solle Eltern, die ihre Kinder nicht impfen, das Kindergeld entziehen!
Da Impfungen schwere Nebenwirkungen haben können, darf kein Staat und keine Institution Eltern vorschreiben dürfen, welche Pharma-Produkte ihren Kindern einverleibt werden!
Um den drohenden Impf-Zwang zu verhindern, rufen wir zur Teilnahme auf und bitten um Unterstützung:
Demonstration am 16.9.2017 in Berlin
FÜR EINE FREIE ZUKUNFT GESUNDER MENSCHEN!
Vaccination must be voluntary!
In many countries of Europe, parents are no longer allowed to decide whether, when and what their children are vaccinated. In Germany, too, the squeeze are being drawn up, and it is currently being discussed that parents who do not vaccinate their children should withdraw child benefit.
Since vaccination can have serious side effects, no state and no institution must be allowed to require parents to have the pharmaceutical products incorporated into their children.
In order to prevent the threat of vaccination, we call to participate and ask for support:
Demonstration on 16.9.2017 in Berlin
For a free future of healthy people!
Movie Vaxxed gets up QUEENSLAND Health Minister’s nose
By Brent Melville
QUEENSLAND Health Minister Cameron Dick was either seriously misinformed, ignorant, or flat out lying when, in response to the touring movie Vaxxed: From Coverup to Catastrophe, he said “there is no shred of credible scientific evidence to support claims that vaccinations are dangerous” (Gold Coast Bulletin, 15/7/17).
The same with Victorian Health Minister Jill Hennessy who stated on Seven News in February last year: “There are no risks in vaccinating your children – the science is really clear”.
Dr Hooker, who joined the Vaxxed tour, says there are in fact more than 100 studies on PubMed on autism, neurological developmental disorders (NDDs) and vaccination. But here’s a few specific studies our blind, deaf and dumb health ministers and their advisers refuse to look at.
1. Neurological and autoimmune disorders after vaccination against pandemic influenza A (H1N1) with a monovalent adjuvanted vaccine: population based cohort study in Stockholm, Sweden. https://www.ncbi.nlm.nih.gov/pubmed/21994316 Conclusion in part: “… Relative risks were significantly increased for Bell’s palsy, paraesthesia, and inflammatory bowel disease after vaccination, predominantly in the early phase of the vaccination campaign…”.
2. Autoimmune disorders (AIDs) after immunisation with Influenza A/H1N1 vaccines with and without adjuvant: EudraVigilance data and literature review. https://www.ncbi.nlm.nih.gov/pubmed/23022149 From abstract: “Of the 50,221 adverse reactions received in EudraVigilance for A/H1N1 vaccines (adjuvanted: 46,173, non-adjuvanted: 4048), 314 were AID (adjuvanted: 276, non-adjuvanted: 38). GBS was the AID with the highest number of reports (125, adjuvanted: 109, non-adjuvanted: 16).
3. Serious adverse events rarely reported after trivalent inactivated influenza vaccine (TIV) in children 6-23 months of age. https://www.ncbi.nlm.nih.gov/pubmed/19450636 From results: “During 1991-2001, VAERS received 128,717 reports…A total of 14.2% of all reports described serious adverse events, which by regulatory definition include death, life-threatening illness, hospitalization or prolongation of hospitalization, or permanent disability.”
4. “Adverse events following Haemophilus influenzae type b vaccines in the Vaccine Adverse Event Reporting System, 1990-2013.” https://www.ncbi.nlm.nih.gov/pubmed/25598306 Study results found: “VAERS received 29,747 reports after Hib vaccines; 5179 (17%) were serious, including 896 reports of deaths. Median age was 6 months (range 0-1022 months). Sudden infant death syndrome was the stated cause of death in 384 (51%) of 749 death reports with autopsy/death certificate records. The most common non-death serious AE categories were neurologic (80; 37%), other noninfectious (46; 22%) (comprising mainly constitutional signs and symptoms); and gastrointestinal (39; 18%) conditions.”
Study: Vaccine Induced Inflammation Cause of Obesity Epidemic – Not Diet
Childhood obesity is now a reason why the state could take away children from their parents. The rationale is that if a child is obese, it is the parents’ fault, because they failed to feed them properly. It is assumed that all childhood obesity is a result of diet.
However, most of us have probably seen first-hand just how different children are when it comes to food and putting on weight. Some children can eat junk food most of the time and never add weight, while some children can eat a healthy, organic diet and still add pounds.
Dr. J. Bart Classen has published a study claiming that the evidence for the overwhelming problem of childhood obesity is not diet, but “vaccine induced inflammation.”
Vaccines, not Diet, are Causing Epidemic of Obesity and Type 2 Diabetes According to New Paper from Classen Immunotherapies
MANCHESTER, Md., June 26, 2017 /PRNewswire/ — A newly published paper in June’s Journal of Endocrinology, Diabetes & Obesity, 5(3): 1107, by immunologist J. Bart Classen, MD of Classen Immunotherapies provides further proof of the dangers of vaccines. The paper reviews the growing evidence that many cases of obesity, type 2 diabetes and metabolic syndrome are inflammatory conditions and that vaccine induced inflammation is the cause of the epidemic of these diseases. Upon receiving a vaccine some individuals’ immune system becomes hyper active leading to autoimmune destruction of insulin secreting cells and the development of type 1 diabetes. Many other individuals produce increased cortisol and other immune suppressing molecules, to suppress the vaccine induced inflammation. This increased production leads to type 2 diabetes, obesity and metabolic syndrome. The new paper reviews evidence supporting vaccines, not diet, as a cause of the epidemics of obesity, type 2 diabetes and metabolic syndrome.
Study – Cause of the Obesity, Type 2 Diabetes and Metabolic Syndrome Epidemics, Vaccine Induced Immune Overload versus Nutrition Overload
Abstract
There is an epidemic of obesity, type 2 diabetes, metabolic syndrome and associated conditions. Patients with these conditions often have markers of
increased inflammation. Many researchers have published that nutrition overload caused the epidemic of obesity and the associated inflammation which
leads to type 2 diabetes and metabolic syndrome. A contrasting view has provided extensive evidence that vaccine induced immune overload has caused an
epidemic of inflammation and this inflammation caused epidemics of obesity, type 2 diabetes and metabolic syndrome. The data reviewed in these manuscripts
provides proof that immune overload, not nutrition overload has been the major contributing factor for the epidemics and inflammation associated with the
epidemics. Several lines of evidence are reviewed including evidence that inflammation precedes obesity in many patients, the lack of inflammation in many
obese patients, an epidemic of inflammation in thin patients, and an epidemic of obesity in children under 6 months of age. The failure to control the obesity
epidemic is blamed on the focus on nutrition and ignoring the root cause, vaccine induced immune overload. Once a patient has developed metabolic syndrome
with type 2 diabetes providers are too frequently subjecting their patients to further immune overload by administering yearly influenza vaccines and many
other vaccines. This action makes metabolic syndrome more difficult to reverse. The plan to reduce obesity must be focused on preventing immune overload
and not blaming patients for their diet. The epidemic of obesity can be reversed through discontinuation of vaccine practices that result in immune overload.
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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✴️ Read all vaccine inserts: tinyurl.com/ReadTheVaccineInsert #RevolutionForChoice #InformedConsent #EducateBeforeYouVaccinate #VAXXED #Polio #TransverseMyelitis #VaccineInjury
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.
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.
the news network 