Jordan Peterson says he spoke to a senior government adviser who told him Canada’s COVID restriction policies are completely driven by opinion polls and not science.
“In relation to the COVID restrictions, I talked to a senior adviser to one of the provincial governments a couple of weeks ago,” said Peterson.
“He told me flat out that the COVID policy here is driven by nothing but opinion polls related to the popularity of the government,” he added.
“No science, no endgame in sight, no real plan, and so what that means is that the part of the population that is most afraid of COVID,” are driving the policy.
Peterson pointed to figures that prove people vastly exaggerate the risk of being hospitalized by COVID due to relentless government fearmongering campaigns.
ODD Reality – They Live | Based on a True Story
These days ‘They Live’ is looking more like Science than it is Fiction. When compared to the world elite or the Illuminati and their obsession with controlling the world and everybody in it, this movie seems like it’s based on a true story.
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.
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.
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