Poliomyelitis

Vaccine News – Study – Varicella Zoster Virus DNA at Inoculation Sites and in Saliva After Zostavax Immunization & VAXXED TV – IT’S NOT JUST THE MMR

Scientists Prove Those Vaccinated for Shingles Can Infect Others with Chicken Pox

US National Library of Medicine
National Institutes of Health – Jun 2011

Study – Varicella Zoster Virus DNA at Inoculation Sites and in Saliva After Zostavax Immunization

Duane L. Pierson,1 Satish K. Mehta,2 Don Gilden,corresponding author4,5 Randall J. Cohrs,4 Maria A. Nagel,4 D. Scott Schmid,6 and Stephen K. Tyring3
1 Space Life Sciences, NASA, Lyndon B. Johnson Space Center
2 Enterprise Advisory Services, Inc
3 University of Texas Health Science Center, Houston, Texas
4 Department of Neurology
5 Microbiology, University of Colorado School of Medicine, Aurora
6 National VZV Laboratory, Centers for Disease Control and Prevention, Atlanta, Georgia

Correspondence: Don Gilden, MD, Department of Neurology, University of Colorado School of Medicine, 12700 E 19th Ave, Box B182, Aurora, CO 80045 (ude.revnedcu@nedlig.nod).

Abstract

Analysis of 36 individuals over age 60 years who were immunized with Zostavax revealed varicella zoster virus (VZV) DNA in swabs of skin inoculation sites obtained immediately after immunization in 18 (50%) of 36 subjects (copy number per nanogram of total DNA, 28 to 2.1 × 106) and in saliva collected over 28 days in 21 (58%) of 36 subjects (copy number, 20 to 248). Genotypic analysis of DNA extracted from 9 random saliva samples identified vaccine virus in all instances. In some immunized individuals over age 60, vaccine virus DNA is shed in saliva up to 4 weeks.
Varicella zoster virus (VZV) is a neurotropic alphaherpesvirus. Primary infection usually causes varicella (chicken pox) in children. Airborne VZV enters the nasopharynx and replicates in tonsillar T cells followed by viremia and skin lesions [1, 2]. After primary infection, VZV becomes latent in neurons of cranial nerve ganglia, dorsal root ganglia, and autonomic ganglia along the entire neuraxis. Decades later, VZV reactivates in elderly and immunocompromised individuals to produce zoster (shingles), a syndrome characterized by pain and a vesicular rash on an erythematous base in 1–3 dermatomes. Zoster is common, with ∼1,000,000 cases annually in the United States. Importantly, zoster is often followed by chronic pain (postherpetic neuralgia [PHN]) as well as by meningoencephalitis, cerebellitis, cranial nerve palsies, vasculopathy, myelopathy, and multiple inflammatory diseases of the eye [3].
To prevent zoster and its attendant neurological complications, Zostavax vaccine (Merck) was approved by the Food and Drug Administration for use in individuals at least 60 years of age. Over a 3-year period, Zostavax effectively reduced the risk of zoster by 51% and PHN by 66% in nearly 20,000 healthy adults age 60 years or older [4]. Zostavax contains live attenuated VZV, and the package insert warns newly vaccinated individuals to avoid contact for an unspecified time with newborn infants, immunosuppressed individuals, and pregnant women who have not had chicken pox or have not been immunized for chicken pox. Because VZV DNA is present in saliva of zoster patients for at least 2 weeks [5] and VZV in saliva can also be infectious [6], we examined the inoculation site and saliva of Zostavax-vaccinated subjects for the presence of VZV DNA for 4 weeks after immunization.

US National Library of Medicine
National Institutes of Health – Aug 1977

Study – Chronic progressive poliomyelitis secondary to vaccination of an immunodeficient child.

Davis LE, Bodian D, Price D, Butler IJ, Vickers JH.

Abstract
We investigated an immunodeficient child in whom chronic progressive poliomyelitis developed after she had received live oral poliovirus vaccine. Poliovirus, Type II, was isolated from throat and stool during life and from several sites within the brain at autopsy. The brain isolate was classified as vaccine-like on the basis of temperature sensitivity and antigenic markers. However, in the monkey neurovirulence test, the brain isolate produced moderately severe lesions throughout the spinal cord and brainstem and appeared nonvaccine-like. Thus, the brain isolate demonstrated a dissociation between the antigenic and neurovirulence markers. Our observations suggest that, under unusual circumstances, such as immunodeficiency, attenuated poliovirus can produce a chronic progressive neurologic disease. This case also emphasizes the need to diagnose immunodeficiency as early as possible, so that live-virus vaccines will not be administered.

Parents in Melbourne

IT’S NOT JUST THE MMR

Gardasil killed my 16 year old daughter

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Brian Hooker on Hit 105 Brisbane radio

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Highwire with Del Bigtree from Australia

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

How to accept Jesus Christ as your personal Saviour

Testimony by Phil Robertson from Duck Dynasty

1 Corinthians 15 Authorized (King James) Version (AKJV)
1 Moreover, brethren, I declare unto you the gospel which I preached unto you, which also ye have received, and wherein ye stand;
2 by which also ye are saved, if ye keep in memory what I preached unto you, unless ye have believed in vain.
3 For I delivered unto you first of all that which I also received, how that Christ died for our sins according to the scriptures;
4 and that he was buried, and that he rose again the third day according to the scriptures:

Hebrews 6 Authorized (King James) Version (AKJV)
1 Therefore leaving the principles of the doctrine of Christ, let us go on unto perfection; not laying again the foundation of repentance from dead works, and of faith toward God,
2 of the doctrine of baptisms, and of laying on of hands, and of resurrection of the dead, and of eternal judgment.
3 And this will we do, if God permit.
4 For it is impossible for those who were once enlightened, and have tasted of the heavenly gift, and were made partakers of the Holy Ghost,
5 and have tasted the good word of God, and the powers of the world to come,
6 if they shall fall away, to renew them again unto repentance; seeing they crucify to themselves the Son of God afresh, and put him to an open shame.
7 For the earth which drinketh in the rain that cometh oft upon it, and bringeth forth herbs meet for them by whom it is dressed, receiveth blessing from God:
8 but that which beareth thorns and briers is rejected, and is nigh unto cursing; whose end is to be burned.

Isaiah 53 – Old testament Prophecy about Jesus

1 Who hath believed our report? and to whom is the arm of the Lord revealed?
2 For he shall grow up before him as a tender plant,and as a root out of a dry ground:he hath no form nor comeliness;and when we shall see him,there is no beauty that we should desire him.
3 He is despised and rejected of men;a man of sorrows, and acquainted with grief:and we hid as it were our faces from him;he was despised, and we esteemed him not.
4 Surely he hath borne our griefs,and carried our sorrows:yet we did esteem him stricken,smitten of God, and afflicted.
5 But he was wounded for our transgressions,he was bruised for our iniquities:the chastisement of our peace was upon him;and with his stripes we are healed.
6 All we like sheep have gone astray;we have turned every one to his own way;and the Lord hath laid on him the iniquity of us all.
7 He was oppressed, and he was afflicted,yet he opened not his mouth:he is brought as a lamb to the slaughter,and as a sheep before her shearers is dumb,so he openeth not his mouth.
8 He was taken from prison and from judgment:and who shall declare his generation? for he was cut off out of the land of the living:for the transgression of my people was he stricken.
9 And he made his grave with the wicked,and with the rich in his death;because he had done no violence,neither was any deceit in his mouth.
10 Yet it pleased the Lord to bruise him;he hath put him to grief:when thou shalt make his soul an offering for sin,he shall see his seed, he shall prolong his days,and the pleasure of the Lord shall prosper in his hand.
11 He shall see of the travail of his soul, and shall be satisfied:by his knowledge shall my righteous servant justify many;for he shall bear their iniquities.
12 Therefore will I divide him a portion with the great,and he shall divide the spoil with the strong;because he hath poured out his soul unto death:and he was numbered with the transgressors;and he bare the sin of many,and made intercession for the transgressors.

The Only Sin That Leads To Hell – Kenneth E Hagin

Vaccine News – VAXXED TV – Stories in northern Auckland & Study – Characterisation of poxviruses from sporadic human infections

Europe’s journal on infectious disease surveillance, epidemiology, prevention and control – 2013

Study – Case of vaccine-associated measles five weeks post-immunisation, British Columbia, Canada, October 2013

M Murti – 1, M Krajden – 2, M Petric – 2, J Hiebert – 3, F Hemming – 1, B Hefford – 4, M Bigham – 1, P Van Buynder – 1

Author Affiliations:
1 Fraser Health Authority, Surrey, British Columbia, Canada
2 Public Health Microbiology and Reference Laboratory British Columbia Centre for Disease Control, Vancouver, British Columbia, Canada
3 National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada
4 1-1400 George St., White Rock, British Columbia, Canada

Case report
We describe a case of vaccine-associated measles in a two-year-old patient from British Columbia, Canada, in October 2013, who received her first dose of measles-containing vaccine 37 days prior to onset of prodromal symptoms. Identification of this delayed vaccine-associated case occurred in the context of an outbreak investigation of a measles cluster.
In this report we describe a case of measles-mumps-rubella (MMR) vaccine-associated measles illness that was positive by both PCR and IgM, five weeks after administration of the MMR vaccine. Based on our literature review, we believe this is the first such case report which has implications for both public health follow-up of measles cases and vaccine safety surveillance.
Between 29 August and 2 September 2013, three unlinked persons from across the Fraser Valley, British Columbia, Canada, presented with rash illness consistent with clinical measles [1]. Based on the outbreak investigation by the local health authority, none of the three cases had an identified exposure to a measles case or travel history outside of Canada during the incubation period, and a source case was never identified. All three cases had the same measles genotype B3 sequence type (MVs/British Columbia.CAN/34.13, MeaNS id 39928, GenBank accession numbers KF704002 and KF704001). Measles genotype B3 is endemic in the World Health Organization’s African and Eastern Mediterranean regions [2]. Two additional cases of measles due to secondary transmission from one of the above cases were identified in British Columbia in the third week of September.

US National Library of Medicine
National Institutes of Health – 1987

Study – Characterisation of poxviruses from sporadic human infections.

Authors
Carra L – 1, Dumbell KR.
Author information
Department of Medical Microbiology, University of Cape Town.

Abstract
An orthopoxvirus was isolated from the vesicular rash of a man in Natal who died in coma and who had not been vaccinated. Analysis of the viral DNA showed that it was a vaccinia virus, more closely related to the virus of South African smallpox vaccine than to other vaccinia viruses. DNA analysis also showed that an orthopoxvirus isolated from a sporadic case of severe pustular rash in Nigeria was a vaccinia virus closely related to the smallpox vaccine virus used there. Minor biological differences between the viruses isolated and the corresponding vaccine strains suggested that some natural transmission of the virus had occurred, but the results of DNA analysis implied that they originated from the use of smallpox vaccine. No similar cases have been detected since smallpox vaccination was discontinued.

US National Library of Medicine
National Institutes of Health – 1989

Study – Acute maternal anterior poliomyelitis in a non-endemic zone

Derenne F – 1, Vanderheyden JE, Bain H, Jocquet P, Jacquy J, Yane F, Druyts-Voets E, Lamy ME, Vanhaeverbeek M.
Author information
Service de Médecine Interne, C.H.U. André Vésale, U.L.B., Montigny-le-Tilleul.

Abstract
The authors report the case of a 26 year old woman with acute anterior poliomyelitis contracted during the vaccination of her baby. Despite having been herself vaccinated in infancy she was not protected against the poliovirus. The clinical interest of this uncommon case is a severe paralytic state with definitive paraplegia. The authors suggest serologic testing of patients born before 1967 especially if they are at risk of encountering the virus.

My own VAXXED/UNVAXXED study

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Interview in a hospital with Sarah Cox

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Meeting Andre and Kazia

Vaccinated vs unvaccinated in Northern Auckland

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Stories in northern Auckland

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

How to accept Jesus Christ as your personal Saviour

Testimony by Phil Robertson from Duck Dynasty

Isaiah 53 – Old testament Prophecy about Jesus

The Only Sin That Leads To Hell – Kenneth E Hagin

Vaccine News – Study – Non-linear dose-response of aluminium hydroxide adjuvant particles: Selective low dose neurotoxicity & VAXXED TV – What My Parents Went Through Is Heartbreaking

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.

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

How to accept Jesus Christ as your personal Saviour

Testimony by Phil Robertson from Duck Dynasty

Isaiah 53 – Old testament Prophecy about Jesus

The Only Sin That Leads To Hell – Kenneth E Hagin

The Cutter Incident: How America’s First Polio Vaccine Led to a Growing Vaccine Crisis

The Cutter Incident: How America’s First Polio Vaccine Led to a Growing Vaccine Crisis
In April 1955 more than 200 000 children in five Western and mid-Western USA states received a polio vaccine in which the process of inactivating the live virus proved to be defective. Within days there were reports of paralysis and within a month the first mass vaccination programme against polio had to be abandoned. Subsequent investigations revealed that the vaccine, manufactured by the California-based family firm of Cutter Laboratories, had caused 40 000 cases of polio, leaving 200 children with varying degrees of paralysis and killing 10.

The sordid history of Poliomyelitis vaccination
By Dr Viera Scheibner (PhD)
International Medical Council on Vaccination
certain facts in the history of polio vaccination:
1. There has been more than one type of polio vaccine through its history, due to the fact that earlier versions were found to be ineffective and harmful.
2. The occurrence of polio was trending downward prior to the introduction of polio vaccines.
3. The reported effectiveness accredited to polio vaccines can actually be easily accounted for by data manipulation and not actual decreases of occurrence. (See also Dr. Suzanne Humphries’ excellent treatment of this subject here: Did Vaccines Really Eradicate Polio?)
4. The history of the polio vaccine is a history of contamination of the vaccines responsible for the injury and deaths of countless people.
Update: The New York Times just published a story recently about new strains of the polio vaccine being developed. Here is what they wrote concerning the current strain of the polio vaccine:
The Sabin vaccine has drawbacks, however: it contains a still-live virus that was mutated long ago so that it is usually too weak to produce disease. In rare cases, it can mutate back into a dangerous form that paralyzes or kills. And the vaccine is risky in children with immune-system problems. For those reasons, the World Health Organization plans to eventually phase it out.

Did Vaccines Really Eradicate Polio?
by Suzanne Humphries, MD
“The tendency of a mass vaccination program is to herd people. People are not cattle or sheep. They should not be herded. A mass vaccination program carries a built-in temptation to oversimplify the problem; to exaggerate the benefits; to minimize or completely ignore the hazards; to discourage or silence scholarly, thoughtful and cautious opposition; to create an urgency where none exists; to whip up an enthusiasm among citizens that can carry with it the seeds of impatience, if not intolerance; to extend the concept of the police power of the state in quarantine far beyond its proper limitation; to assume simplicity when there is actually great complexity; to continue to support a vaccine long after it has been discredited;… to ridicule honest and informed consent.[1]”
Now it is admitted in the medical literature that other viruses can cause polio, yet few people on the street have any idea.
Prior to 1954, the following undoubtedly hid behind the name “poliomyelitis”: Transverse Myelitis, viral or “aseptic” meningitis, Guillain-Barre Syndrome (GBS)- (what Franklin Delano Roosevelt had)[4], Chinese Paralytic syndrome, Chronic Fatigue Syndrome, epidemic cholera, cholera morbus, spinal meningitis, spinal apoplexy, inhibitory palsy, intermittent fever, famine fever, worm fever, bilious remittent fever, ergotism, post-polio syndrome, acute flaccid paralysis(AFP).
Included under the umbrella term “Acute Flaccid Paralysis” are Poliomyelitis, Transverse Myelitis, Guillain-Barré syndrome, enteroviral encephalopathy, traumatic neuritis, Reye’s syndrome etc.
Before you believe that polio has been eradicated, have a look at this graph of AFP and Polio.
Does the public have any idea that there are hundreds of cases of something that would once have been called polio, and some of those children will be dependent on a modern version of the iron lung? No. Parents today think that the Salk vaccine eliminated any need for ventilators, because the pictures of all these children on iron lungs are no longer paraded in front of people in order to create fear. Besides which, today’s “iron lungs” don’t look like a prototype submarine. They are barely recognizable as today’s “ventilators.”
The polio vaccine had the fastest licensing in FDA history. It was approved for commercial production after only a two-hour deliberation amongst the Licensing Committee, in a pressured environment. These scientists witnessed a vaccine that was escorted to market, before academic and community doctors had a chance to read any published reports on the safety studies, and before the results of the big polio vaccine trial made it into any medical journal. If these scientists had had more say, it is likely that the “Cutter” disaster and the “Wyeth problem,” both events that led to crippling or death of vaccine recipients just weeks following the hurried vaccine licensing – could have been averted.
“Previously it [the vaccine] had been distributed as an experimental product, not a licensed product…the committee was asked to come to a decision very quickly…there was discussion of the report that Dr Francis had given, but we were not in a position to discuss it very intensively because we had not seen the report prior to this morning and the report was distributed to us after the presentation…we were pressured in the sense that we were told that speed was essential, and when we came up toward the 5:00 time, some of us felt we would like to discuss this matter more. We were told that to discuss the matter further it would have to go into the following week, and we would have to go to Washington or Bethesda and most of the members were unwilling to do so. We were in effect pressured into an earlier decision than we ordinarily would have made. …It was part of the pressure of events, put it that way.[5]”
And that is only the beginning of the polio story, the likes of which currently serve as the foundation of modern belief in vaccination, even by those who may have doubts regarding current vaccine policy.

The Current Vaccine Reality: Disinformed Consent

We are living in the age of disinformed consent. Parents assume their doctors and their public health authorities are providing them with all relevant vaccine information, and nothing could be further from the truth.

Obviously, if vaccines can kill and cause serious and debilitating lifelong damage – which they can, and do – the vaccine administrator must provide that information to the client, in unambiguous fashion, regardless of the estimated size of the risk. It’s an ethical mandate that must be fulfilled, but it never is. There is a fundamental reason: medical schools don’t teach the history and nature of vaccine damage and death; nor do nursing and pharmacy schools. Yet doctors, nurses, and, these days, pharmacists, are the very ones who administer vaccines, and upon whom we rely for full information. Somewhere there is made a conscious decision to exclude the reality of serious vaccine damage from the curricula.

Most of the many doctors who have witnessed vaccine damage – thankfully, not all – lack the professional integrity to follow up with curiosity, let alone research. This is the most troubling of the array of vaccine contradictions; trained to observe, they nevertheless appear blind to even the possibility of causal relation.

There is a reason the CDC didn’t announce to the American public in 1999 the direct correlation between the amount of mercury in vaccines and the incidence of speech and learning disorders and autism it found in its own in-house study: a conscious, intolerable decision. [1]

There’s a reason Dr. Viera Scheibner’s cotwatch studies, which decades ago found a compelling link between vaccinations given to infants and the incidence of cot death – SIDS – is never mentioned by public health officials: a conscious decision. [2]

There is a reason the CDC never mentions that it was the radical changes they made to the definition and diagnosis of polio, right after the vaccine was introduced, that eliminated most cases of the disease, not the vaccine: a conscious decision to manipulate the public in their vaccine decisions. Nor do they mention that once the vaccine was licensed, the CDC pulled all remaining diagnoses close to the vest, disallowing for automatic inclusion in annual polio statistics cases reported by private medical practices or local public health departments, and declaring that only they, the CDC, after ostensible thorough review and lab analysis, could officially validate a case. [3]

There is a reason that, concomitant with the diagnostic and labeling changes made, a radical change was made as well to the definition of a polio epidemic, from 20 cases in 100,000 to 35, potentially cutting almost in half the likelihood that any subsequent outbreaks would be so labeled – a change that seems totally haphazard, except for the effect of painting polio as somehow and suddenly less severe, or less contagious, or more contained: a conscious decision, to boost the illusion of vaccine effectiveness. [3]

There’s a reason the mainstream media in general will give no meaningful column space to truthful information about vaccine pitfalls and dangers: the conscious decision of the publishers.

The Current Vaccine Reality: Disinformed Consent (naturalblaze.com)
The Current Vaccine Reality: Disinformed Consent (oneworldchronicle.com)
How the Current Medical System Misinforms You About Vaccines (vactruth.com)
Current Vaccine Reality: Disinformed Consent (intellihub.com)
Bill Gates’ Polio Vaccine Program Eradicates Children, Not Polio (pakalertpress.com)
Bill Gates’ Polio Vaccine Program Eradicates Children, Not Polio (naturalblaze.com)
The Current Vaccine Reality: Disinformed Consent (activistpost.com)
The current vaccine reality: Disinformed consent (sott.net)
The Current Vaccine Reality: Disinformed Consent (forum.prisonplanet.com)

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Poliomyelitis

Vaccine News – Study – Varicella Zoster Virus DNA at Inoculation Sites and in Saliva After Zostavax Immunization & VAXXED TV – IT’S NOT JUST THE MMR

Vaccine News – VAXXED TV – Stories in northern Auckland & Study – Characterisation of poxviruses from sporadic human infections

Vaccine News – Study – Non-linear dose-response of aluminium hydroxide adjuvant particles: Selective low dose neurotoxicity & VAXXED TV – What My Parents Went Through Is Heartbreaking

The Cutter Incident: How America’s First Polio Vaccine Led to a Growing Vaccine Crisis

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