Tag Archives: Andrew Wakefield
“I apologize again for the price you paid for my dishonesty…”–CDC Whistleblower Dr. William Thompson to Dr. Andrew Wakefield.
Wakefield- “Is the Press Release real”?
Wakefield: “Thank You. It was the right and honorable thing to do”.
Thompson: “I agree. I apologize for the price you paid for my dishonesty”.
Wakefield: “I forgive you completely and without any bitterness”.
Thompson: I know you mean it and I am grateful to know you more personally.
The last desperate effort when the CDC whistle blower story broke last week was for the vaccine establishment and media to drive a wedge between Dr. Thompson and Dr. Andrew Wakefield, whose “fraud” (according to British journalist Brian Deer) has been made to carry the sins of the entire vaccine industry for many years. Dr. Wakefield shared two text messages with The Truth Barrier that he and his wife received from Dr. Thompson.
The first one was to Dr. Wakefield’s wife, Carmel, and it read: “I do believe your husbands career was unjustly damaged and this study would have supported his scientific opinion. Hopefully I can help repair it”.—Text exchange between Dr. Andrew Wakefield and Dr. William Thompson, Aug 27, 2014
Polly Tommey, Director of Autism Media Channel, told The Truth Barrier there are more whistle blowers trying to find the courage, and or, the legal protection, to speak.
“There are more whistleblowers coming out,” she said. “We know who they are and we’ve spoken to them. They’re petrified. These sources make Thompson pale in comparison, some of them. They know the MMR is a massive problem, data has been corrupted, they’ve been told to hide things…”
Comment: One guy spoke about Gardisil. He said, ‘You can forget about MMR—Gardisil is one of the biggest crimes ever. 144 girls or something have died already. Thompson is only the beginning. “
CDC Admits 98 Million Americans Received Polio Vaccine In An 8-Year Span When It Was Contaminated With Cancer Virus
July 17, 2013 by DAVE MIHALOVIC
SV40 is an abbreviation for Simian vacuolating virus 40 or Simian virus 40, a polyomavirus that is found in both monkeys and humans. Like other polyomaviruses, SV40 is a DNA virus that has been found to cause tumors and cancer.
SV40 is believed to suppress the transcriptional properties of the tumor-suppressing genes in humans through the SV40 Large T-antigen and SV40 Small T-antigen. Mutated genes may contribute to uncontrolled cellular proliferation, leading to cancer.
Michele Carbone, Assistant Professor of Pathology at Loyola University in Chicago, has recently isolated fragments of the SV-40 virus in human bone cancers and in a lethal form of lung cancer called mesothelioma. He found SV-40 in 33% of the osteosarcoma bone cancers studied, in 40% of other bone cancers, and in 60% of the mesotheliomas lung cancers, writes Geraldo Fuentes.
Dr. Michele Carbone openly acknowledged HIV/AIDS was spread by the hepatitis B vaccine produced by Merck & Co. during the early 1970s. It was the first time since the initial transmissions took place in 1972-74, that a leading expert in the field of vaccine manufacturing and testing has openly admitted the Merck & Co. liability for AIDS.
The matter-of-fact disclosure came during discussions of polio vaccines contaminated with SV40 virus which caused cancer in nearly every species infected by injection. Many authorities now admit much, possibly most, of the world’s cancers came from the Salk and Sabin polio vaccines, and hepatitis B vaccines, produced in monkeys and chimps.
It is said mesothelioma is a result of asbestos exposure, but research reveals that 50% of the current mesotheliomas being treated no longer occurs due to asbestos but rather the SV-40 virus contained in the polio vaccination. In addition, according to researchers from the Institute of Histology and General Embryology of the University of Ferrara, SV-40 has turned up in a variety other tumors. By the end of 1996, dozens of scientists reported finding SV40 in a variety of bone cancers and a wide range of brain cancers, which had risen 30 percent over the previous 20 years.
The SV-40 virus is now being detected in tumors removed from people never inoculated with the contaminated vaccine, leading some to conclude that those infected by the vaccine might be spreading SV40.
Soon after its discovery, SV40 was identified in the oral form of the polio vaccine produced between 1955 and 1961 produced by American Home Products (dba Lederle).
Both the oral, live virus and injectable inactive virus were affected. It was found later that the technique used to inactivate the polio virus in the injectable vaccine, by means of formaldehyde, did not reliably kill SV40.
Just two years ago, the U.S. government finally added formaldehyde to a list of known carcinogens and and admitted that the chemical styrene might cause cancer. Yet, the substance is still found in almost every vaccine.
According to the Australian National Research Council, fewer than 20% but perhaps more than 10% of the general population may be susceptible to formaldehyde and may react acutely at any exposure level. More hazardous than most chemicals in 5 out of 12 ranking systems, on at least 8 federal regulatory lists, it is ranked as one of the most hazardous compounds (worst 10%) to ecosystems and human health (Environmental Defense Fund).
In the body, formaldehyde can cause proteins to irreversibly bind to DNA. Laboratory animals exposed to doses of inhaled formaldehyde over their lifetimes have developed more cancers of the nose and throat than are usual.
Facts Listed on The CDC Website about SV40
- SV40 is a virus found in some species of monkey.
- SV40 was discovered in 1960. Soon afterward, the virus was found in polio vaccine.
- SV40 virus has been found in certain types of cancer in humans.
- In the 1950s, rhesus monkey kidney cells, which contain SV40 if the animal is infected, were used in preparing polio vaccines.
- Not all doses of IPV were contaminated. It has been estimated that 10-30 million people actually received a vaccine that contained SV40.
- Some evidence suggests that receipt of SV40-contaminated polio vaccine may increase risk of cancer.
A Greater Perspective on Aerial Spraying and SV40
The Defense Sciences Office of the Pathogen Countermeasures Program, in September 23, 1998 funded the University of Michigan’s principal investigator, Dr. James Baker, Jr. Dr. Baker, Director of Michigan Nanotechnology Institute for Medicine and Biological Sciences under several DARPA grants. Dr. Baker developed and focused on preventing pathogens from entering the human body, which is a major goal in the development of counter measures to Biological Warfare. This research project sought to develop a composite material that will serve as a pathogen avoidance barrier and post-exposure therapeutic agent to be applied in a topical manner to the skin and mucous membranes. The composite is modeled after the immune system in that it involves redundant, non-specific and specific forms of pathogen defense and inactivation. This composite material is now utilized in many nasal vaccines and vector control through the use of hydro-gel, nanosilicon gels and actuator materials in vaccines.
Through Dr. Baker’s research at the University of Michigan; he developed dendritic polymers and their application to medical and biological science. He co-developed a new vector system for gene transfer using synthetic polymers. These studies have produced striking results and have the potential to change the basis of gene transfer therapy. Dendrimers are nanometer-sized water soluble polymers that can conjugate to peptides or arbohydrates to act as decoy molecules to inhibit the binding of toxins and viruses to cells. They can act also as complex and stabilize genetic material for prolonged periods of time, as in a “time released or delayed gene transfer”. Through Dr. Baker’s ground breaking research many pharmaceutical and biological pesticide manufacturers can use these principles in DNA vaccines specific applications that incorporate the Simian Monkey Virus SV40.
WEST NILE VIRUS SPRAYING
In 2006 Michael Greenwood wrote an article for the Yale School of Public Health entitled, “Aerial Spraying Effectively Reduces Incidence of West Nile Virus (WNV) in Humans.” The article stated that the incidence of human West Nile virus cases can be significantly reduced through large scale aerial spraying that targets adult mosquitoes, according to research by the Yale School of Public Health and the California Department of Public Health.
Under the mandate for aerial spraying for specific vectors that pose a threat to human health, aerial vaccines known as DNA Vaccine Enhancements and Recombinant Vaccine against WNV may be tested or used to “protect” the people from vector infection exposures. DNA vaccine enhancements specifically use Epstein-Barr viral capside’s with multi human complement class II activators to neutralize antibodies. The recombinant vaccines against WNV use Rabbit Beta-globulin or the poly (A) signal of the SV40 virus. In early studies of DNA vaccines it was found that the negative result studies would go into the category of future developmental research projects in gene therapy. During the studies of poly (A) signaling of the SV40 for WNV vaccines, it was observed that WNV will lie dormant in individuals who were exposed to chicken pox, thus upon exposure to WNV aerial vaccines the potential for the release of chicken pox virus would cause a greater risk to having adult onset Shingles.
CALIFORNIA AERIAL SPRAYING for WNV and SV40
In February 2009 to present date, aerial spraying for the WNV occurred in major cities within the State of California. During spraying of Anaheim, CA a Caucasian female (age 50) was exposed to heavy spraying, while doing her daily exercise of walking several miles. Heavy helicopter activity occurred for several days in this area. After spraying, she experienced light headedness, nausea, muscle aches and increased low back pain. She was evaluated for toxicological mechanisms that were associated with pesticide exposure due to aerial spraying utilizing advanced biological monitoring testing. The test results which included protein band testing utilizing Protein Coupled Response (PCR) methods were positive for KD-45. KD-45 is the protein band for SV-40 Simian Green Monkey virus. Additional tests were performed for Epstein-Barr virus capside and Cytomeglia virus which are used in bioengineering for gene delivery systems through viral protein envelope and adenoviral protein envelope technology. The individual was positive for both; indicating a highly probable exposure to a DNA vaccination delivery system through nasal inhalation.
The question of the century is how many other viruses and toxins are within current day vaccines that we’ll only find out about in a few decades?
Full statement by MMR scare doctor Andrew Wakefield: ‘The Government has tried to cover up putting price before children’s health’
This is the full statement from Andrew Wakefield, the discredited doctor whose Lancet article sparked the MMR scare 15 years ago, on the outbreak of measles in Wales.
In the wake of further media distortion, misrepresentation, and ignorance in relation to the measles outbreak in Wales, it is important to clarify some key facts.In 1998, following an analysis of all published pre-licensing studies of MMR vaccine safety I recommended the use of single measles vaccine in preference to MMR. This remains my position.
At that time, in contrast with the false assertions of many commentators, including Richard Horton, Editor of The Lancet, and vaccine millionaire Paul Offit, the single vaccines were licensed in the UK and freely available to the British public.
While MMR vaccination uptake fell from February 1998, there was a reciprocal increase in the uptake of the single vaccines – a fact that is never acknowledged in the press. Vaccination clinics administered many thousands of doses of measles vaccine and children were “protected”.
Six months later, in September 1998, the British government withdrew the importation licence for the single vaccines, effectively blocking this option for parents.
Measles cases in the UK rose when the government withdrew the importation licence for the single measles vaccine leaving concerned parents with no choice. When I demanded to know why, if the government’s principal concern was to protect children from measles, it would prevent parents with genuine safety concerns over MMR from protecting their children, Elizabeth Miller of the Health Protection Agency responded, “…if we allowed parents the choice of single measles vaccines it would destroy our MMR programme.” The government’s concern appeared to be to protect the MMR programme over and above the protection of children.
Despite the claim of David Salisbury, head of the UK’s Immunisation Division, that MMR has, “an exemplary safety record”, two of the three brands introduced in 1988 had to be withdrawn for safety reasons – they caused meningitis.
Government officials had approved these dangerous vaccines – Pluserix and Immravax – giving them the great majority of the UK market despite knowing that they were high risk and despite having been warned explicitly of their dangers. These government officials put price before children’s health and have been seeking to cover up this shameful fact ever since.
The US government has paid out millions of dollars to children whose autism followed vaccine-induced brain damage. A recent government concession in the US Vaccine Court confirms that the parents’ claims were valid all along. In a recently published December 13, 2012 vaccine court ruling, hundreds of thousands of dollars were awarded to Ryan Mojabi, whose parents described how “MMR vaccinations”, caused a “severe and debilitating injury to his brain, diagnosed as Autism Spectrum Disorder [‘ASD’]”.
Later the same month, the government suffered a second major defeat when young Emily Moller from Houston won compensation following vaccine-related brain injury that, once again, involved MMR and resulted in autism.
The cases follows similar successful petitions in the Italian and US courts (including Hannah Poling, Bailey Banks, Misty Hyatt, Kienan Freeman, Valentio Bocca, and Julia Grimes) in which the governments conceded or the court ruled that vaccines had caused brain injury. In turn, this injury led to an ASD diagnosis. MMR vaccine was the common denominator in these cases.
The more light that shone on this subject by way of informed, balanced debate, the better. I am offering to debate any serious challenger on MMR vaccine safety and the role of MMR in autism, live, in public, and televised
Post Vaccination – Vaccine Targeted Strain – Viral and Bacterial Pathogen – Shedding
So how much of this said claim is truth and real, and/or not real? Do we know? A search for the evidence.
First of all, let me ask this. Why is it, that when the conclusions of actually peer reviewed studies are not in your favor as to the intended agenda bias, that even endless peer reviewed studies are not enough to get pro-vaccine people to take a look at and even read a single one of those studies; yet when there are limited to little to no existing peer reviewed studies, that they are jumping all over with demands to produce a peer reviewed study, to make such as any certain such as a vax-truth opposing persons point of contention, that has expressed?
In regard to vaccines lets go to the issue of vaccine shedding, and ask the question as to can and do any of the current vaccines shed the pathogen in a way that could make a non vaccinated person susceptible to acquiring the illness from a vaccinated person. There are in Pubmed several but limited studies that address the shedding issue as to in regard to the various vaccines. Just use the search terms vaccine shedding Pubmed, and will you several but as said limited numbers references in the google listing, and then you can go to pubmed itself, which is somewhat as well limited for available references as to claiming one way or the other. As for the measles vaccine, one Pubmed reference stated that it the vaccine could shed for up to three days. Certainly long enough to infect another individual.
So, actually and possibly no one really nor likely knows for sure what the complete truth is on this issue. It would seem to be common sense that the vaccine makers surely do not and would not want to know if their vaccine causes shedding or not; nor to find out. So then who would actually fund theses said studies. I think with what I read and reviewed in regard to vaccine shedding, just getting into even the beginning phase of the studies, tells me that vaccines do have a potential to shed irregardless of being bacterial or viral; which very well could be an obvious risk to the unvaccinated. I mean good grief, the existing studies clearly point to the push to vaccinate everyone due to the risk of shedding possibility. What more evidence would you need of the risk of the vaccinated, to the unvaccinated? And yet the pro-vaccine side wants to claim to just the opposite; and that it is only the vaccinated that are at risk from the unvaccinated??? You know accused again of reducing the vaccine derived herd immunity; even though the schools most often even today have no more than a 5% or less rate of existing school exemptions? We as well by the way are not are NOT just talking about the oral polio vaccine, here. They clearly know that the oral polio vaccine sheds and can as well cause numerous cases of AFP in the underdeveloped and unsanitary for conditions countries, that the oral polio vaccine is still used to day. They know of the identified mutations in the polio vaccine virus that the the said oral vaccine has very likely as well caused. if they have an alternative explanation, I have yet to hear and or read about it.
So, let me ask you, have vaccines eradicated so called illness and disease, or have they just prolonged the exit, while creating only lower levels of chronic disease, and disease conditions? How about other unrelated chronic illness and autoimmune disease, unrelated to the vaccine targeted pathogen? How about the pubmed listed as well references to the harm of aluminum adjuvants, causing overactivation of the brains microglia and resulting low levels of chronic brain inflammation resulting for repeat multiple vaccines, in some individuals; maybe more individuals and children that we have ever realized? How about the aluminum adjuvant connection to ASD? The studies, and new studies have shown that same brain inflammation to now be found in more and more children and individuals with ASD. And they want to tell us that vaccines have never been scientifically linked in any study, to ASD? Really? How about the MMR vaccine, in which there are actually some similar physiological pathways found in relation to ASD, and also which are in common with heavy metal toxicity, if not overload, in regard to both thimerosal, and aluminum adjuvants. I don’t know about you and what you think, but I think it is not looking good for the claim as to the issue of vaccines doing more good than harm. When will the CD stop living in the dark ages, and dragging their feet as to doing the proper studies? Yet they waste millions chasing the genetic link to ASD, and refuse all other types and forms of real research?
I did pick one specific peer reviewed reference in regard shedding, that I thought was interesting, and a bit troublesome regarding risk. In regard to the shedding of course all they can come up with is to come up with that every last person existing must be vaccinated to protect them against the shedding.
Pertussis infection in fully vaccinated children in day-care centers, Israel.
We tested 46 fully vaccinated children in two day-care centers in Israel who were exposed to a fatal case of pertussis infection. Only two of five children who tested positive for Bordetella pertussis met the World Health Organization’s case definition for pertussis. Vaccinated children may be asymptomatic reservoirs for infection.
Pertussis Vaccine Failure is not Just Modern but Historical: Vaccine has Never Been Effective
Researchers find first US evidence of vaccine-resistant pertussis
And they tell us the vaccines do not shed? How would this be possible if the vaccines do not shed anything contagious? And they want us to believe that the un-vaccinated are a risk to the vaccinated. Vaccine derived herd relatively and comparatively short term immunity, has never had any actual science behind it; and as to natural long term and/or life time immunity, where as that concept actually makes does sense. So what is the REAL reason they say they need vaccine derived herd immunity? Is it possible that it is more likely due to the issue of vaccine shedding? Now we are getting to some actual understanding of what possibly really goes on.
17 Examples of Admitted Vaccine Failure
Nine cases of eczema vaccinatum are presented, including two fatalities. Seven were caused by contact of a child with eczema with a recently vaccinated sibling.
Suddenly appearing umbilicated vesicles superimposed upon atopic eczema are almost diagnostic of eczema vaccinatum or eczema herpeticum. These do not occur with mere secondary bacterial infection.
Hyperimmune vaccinal gamma-globulin is now available for specific therapy.
Eczema vaccinatum is frequently iatrogenic and uniformly preventable.
The following steps are recommended for prophylaxis: 1) No child with atopic eczema or other skin disorder should be vaccinated. 2) No child should be vaccinated if any member of his family has eczema or other skin disorder. 3) Parents of children with eczema should be notified at the onset of the disease of the danger from vaccination contact. 4) If a sibling of a child with atopic eczema is vaccinated, he must be completely separated from that child for at least 21 days. 5) Forms used by state and local health departments for parents’ consent to vaccination should include an appropriate warning of the contraindications. 6) Eczema vaccinatum should be a reportable disease. 7) Patients recently vaccinated must be excluded from pediatric wards containing patients with atopic eczema, other diseases of the skin, burns or healing surgical incisions. 8) Vaccination may be recommended at 2 months of age, especially for babies from strongly allergic families.
Acellular pertussis vaccination enhances B. parapertussis colonization
An acellular whooping cough vaccine actually enhances the colonization of Bordetella parapertussis in mice; pointing towards a rise in B. parapertussis incidence resulting from acellular vaccination, which may have contributed to the observed increase in whooping cough over the last decade.
And rarely are they testing for it nor even knowing understanding what pertussis pathogen strains are there. B parapertussis antigen is not in the current vaccine. And the fear mongering and the recommended boosters continue.
They can admit to the pertussis vaccine failure in Pakistan, but the CDC can not and refuses to admit to that here happening in the US.
Public Health. 2012 Jun;126(6):518-22. doi: 10.1016/j.puhe.2012.02.001. Epub 2012 Mar 23.
Pertussis resurgence among vaccinated children in Khairpur, Sindh, Pakistan.
Mughal A, Kazi YF, Bukhari HA, Ali M.
Source:Diagnostic and Research Centre, Department of Microbiology, Shah Abdul Latif University, Khairpur, Sindh, Pakistan.
To investigate the aetiology of persistent cough among vaccinated children as suspected cases of pertussis in Khairpur District, Sindh, Pakistan. Pertussis or whooping cough, caused by Bordetella pertussis, is re-appearing in many countries despite vaccination coverage. In Khairpur, persistent cough and symptoms similar to pertussis among vaccinated children are common but the aetiology has not been investigated previously.
B. pertussis was isolated from cough samples of suspected pertussis patients (n = 700) using the cough plate method with charcoal agar.
Isolation and confirmation of the clinical isolates of B. pertussis was performed by culture on Bordet-Gengou medium, biochemical tests and polymerase chain reaction.
In total, 22 strains of B. pertussis were isolated from clinical cough samples.
To the authors’ knowledge, this is the first report of the presence of pertussis in vaccinated children in Khairpur. There is a need for continuous monitoring of pertussis after immunization programmes in order to assess the efficacy of pertussis vaccination.
And what has the CDC done about it all? They have only continued with their fear mongering and falsely blaming the un-vaccinated. Cocoon tyle vaccinating whole families, and still the outbreaks occur.
The False Theory of Vaccine Derived – Herd Immunity
Whooping Cough Epidemic Caused by Virulent New Pertussis Strain—And It’s the Result of Vaccine
Bordetella pertussis Strains with Increased Toxin Production Associated with Pertussis Resurgence (PDF)
We present evidence that in the Netherlands the dramatic increase in pertussis is temporally associated with the emergence of Bordetella pertussis strains carrying a novel allele for the pertussis toxin promoter, which confers
increased pertussis toxin (Ptx) production. Epidemiologic data suggest that these strains are more virulent in humans. We discuss changes in the ecology of B. pertussis that may have driven this adaptation. Our results underline the importance of Ptx in transmission, suggest that vaccination may select for increased virulence, and indicate ways to control
J Hyg (Lond). 1976 August; 77(1): 85–91.
Prevalent serotypes of Bordetella pertussis in non-vaccinated communities.
In many countries, the prevalent serotypes of Bordetella pertussis have changed from a mixture of types 1,2,3 and 1,2 (organisms possessing antigen 2) to a predominance of type 1,3. The timing of the change in different countries is shown to be related to the introduction of mass-vaccination with material rich in antigens 1 and 2 but weak in, or devoid of, antigen 3. In several parts of the world, there have been outbreaks of type 1,3 infection in fully vaccinated children. Non-vaccinated communities in various parts of the world still show the pattern of serotypes which existed elsewhere before mass-vaccination. In order to avoid the disappointments experienced in the past, it is essential that pertussis vaccine for use in previously non-vaccinated communities, like that for any other country, should be rich in each of the three antigens.
Small Mutations in Bordetella pertussis Are Associated with Selective Sweeps
Our results suggest that the B. pertussis gene repertoire is already well adapted to its current niche and required only fine tuning to persist in the face of vaccination. Further, this work shows that small mutations, even single SNPs, can drive large changes in the populations of bacterial pathogens within a time span of six to 19 years.
You can not patent vitamin C, as you can an expensive drug or vaccine. Modern medicine is NOT about the actual health of your child, unless it can be done with chemical pharma.
Special Report: The Vitamin C Treatment of Whooping Cough (Pertussis)
Here is what they already knew years ago in the treatment of pertussis.
Can Med Assoc J. 1937 August; 37(2): 134–136.
Ascorbic Acid (Vitamin C) Treatment of Whooping Cough *
The short series of cases presented is too small to draw any statistical conclusions, but one fact stands out. Ascorbic acid has a definite efTect in shortening the period of paroxysms from a matter of weeks to a matter of days. We have not checked by cough plates or otherwise in this preliminary work to see whether the infectivity subsides simultaneously with the spasmodic symptoms, but are continuing with a larger series of cases in which these and other tests will be employed.
The dosages used have been empirical, with a tendency to use larger doses early in the disease as our experience of its effects progressed. The acid is available at reasonable prices, and the danger of overdosage seems negligible. Animals have received 2,000 times their estimated requirements without any deleterious effects. Any excess is excreted by the kidneys.
1. A method has been described for the treatment of whooping cough by ascorbic acid
2. Ascorbic acid definitely shortens the paroxysmal stage of the disease, particularly if
Pertussis is a bacteria, but either way it is beneficial.
Vitamin C As An Antiviral: It’s All About Dose
Vitamin C for Whooping Cough. Updated Edition. Suzanne Humphries, MD
Why is nobody studying vitamin C in whooping cough? – Conventional medicine’s hypocrisy. by Suzanne Humphries, MD
LIPOSOMAL ENCAPSULATED VITAMIN C
History Repeats Itself: Lessons Vaccinators Refuse to Learn, by Jennifer Craig, PhD
Another below is another example of a failed effort with polio vaccine. It does little good to claim to have eliminated a certain number of previously present cases of polio, while at the same time causing massive cases of polio vaccine derived paralysis. 47,500 new cases. Yet they claim this is NECESSARY, to eradicate polio. They refuse to admit any failure, it seems to me?
Indian J Med Ethics. 2012 Apr-Jun;9(2):114-7.
Polio programme: let us declare victory and move on.
Vashisht N, Puliyel J.
Source:Department of Paediatrics, St Stephens Hospital, Delhi 110054, India.
It was hoped that following polio eradication, immunisation could be stopped. However the synthesis of polio virus in 2002, made eradication impossible. It is argued that getting poor countries to expend their scarce resources on an impossible dream over the last 10 years was unethical. Furthermore, while India has been polio-free for a year, there has been a huge increase in non-polio acute flaccid paralysis (NPAFP). In 2011, there were an extra 47,500 new cases of NPAFP. Clinically indistinguishable from polio paralysis but twice as deadly, the incidence of NPAFP was directly proportional to doses of oral polio received. Though this data was collected within the polio surveillance system, it was not investigated. The principle of primum-non-nocere was violated. The authors suggest that the huge bill of US$ 8 billion spent on the programme, is a small sum to pay if the world learns to be wary of such vertical programmes in the future.
VIDS – Vaccine Induced Diseases
51 035 cases of AFP appear in this document (p 578) for India in 2011, and the in 2011. The figure of 86 638 cases of AFP was listed as globally.
VRM: The Re-emergence of Polio in The Third World (compliments of the World Health Organization & Bill Gates)
VRM: Weaponized Polio & The African Green Monkey Conundrum
Why I choose not to Vaccinate my child
by: Amy Goalen Whittam
What Is Coming Through That Needle? The Problem of Pathogenic Vaccine Contamination
Mutant Polio Virus Spreads in Nigeria
Experts have long believed epidemics unleashed by a vaccine’s mutated virus wouldn’t last since the vaccine only contains a weakened virus strain – but that assumption is coming under pressure. Some experts now say that once viruses from vaccines start circulating they can become just as dangerous as wild viruses.
“The only difference is that this virus was originally in a vaccine vial,” said Olen Kew, a virologist at the U.S. Centers for Disease Control and Prevention.
The oral polio vaccine used in Nigeria and elsewhere contains a mild version of the live virus. Children who have been vaccinated pass the virus into the water supply through urine or feces. Other children who then play in or drink that water pick up the vaccine’s virus, which gives them some protection against polio.
But in rare instances, as the virus passes through unimmunized children, it can mutate into a strain dangerous enough to ignite new outbreaks, particularly if immunization rates in the rest of the population are low.
Kew said genetic analysis proves mutated viruses from the vaccine have caused at least seven separate outbreaks in Nigeria.
Though Nigeria’s coverage rates have improved, up to 15 percent of children in the north still haven’t been vaccinated against polio. To eradicate the disease, officials need to reach about 95 percent of the population.
Nigeria’s vaccine-linked outbreak underlines the need to stop using the oral polio vaccine as soon as possible, since it can create the very epidemics it was designed to stop, experts say. WHO is researching other vaccines that might work better, but none is on the horizon.
Until a better vaccine is ready, WHO and U.S. CDC officials say the oral vaccine is the best available tool to eradicate polio and that when inoculation rates are nearly 100 percent it works fine.
“Nigeria is almost a case study in what happens when you don’t follow the recommendations,” Kew said.
Mutated Polio From Vaccine Is Spreading in Africa
A mutation from a live polio vaccine is stalking Nigeria. In a strange twist of logic, experts are claiming that it mutated as it passed through non-immunized children.
The claim is that children given the live attenuated oral vaccine are properly immunized, but the live virus passes through them and enters local water supplies through their urine or feces. Then, children who have not been immunized pick up the supposedly safe virus by drinking or playing in the water. The weakened virus mutates in them, becoming a new virulent strain.
Why the virus would choose to mutate in non-vaccinated, rather than vaccinated, children is unexplained. Even odder is why the weakened virus would pass through the vaccinated children. If the purpose of a live attenuated vaccination is to force the body to develop antibodies to the virus, then why would live viruses be excreted? Shouldn’t they be killed by the newly-developed antibodies?
Are we being lied to?
This sounds much like the argument that blames nonvaccinated people for disease in those who’ve submitted to innoculations. If the vaccines are effective, then why would the vaccinated be at risk from the unvaccinated?
Are we being lied to?
Nigeria Sees Polio Outbreak from Mutated Vaccine Virus
Polio in Nigeria Traced to Mutating Vaccine
Mutated virus confirms polio vaccine fears. New Delhi
Vaccine. 1994 May;12(6):503-7.
Point mutations involved in the attenuation/neurovirulence alternation in type 1 and 2 oral polio vaccine strains detected by site-specific polymerase chain reaction.
We screened for this mutation in five type 1 and nine type 2 polio vaccine-derived strains isolated from vaccine-associated paralytic poliomyelitis (VAPP) cases and in 16 such strains isolated from healthy vaccinees. All 14 strains isolated from VAPP presented the reversion. Of the eight pairs of type 1 isolates from healthy vaccinees, four presented the reversion 3 days after vaccine administration and all but one at 7 days postvaccination. These results support the involvement of the 5′ non-coding specific nucleotide sites in the reversion to neurovirulence of attenuated polio vaccine strains upon multiplication in the human gut
Look at the unbelievable statements in the next set of information. So ask, WHY are they using a live and shedding viral vaccine, in these contaminated areas, at all?
Oral Polio Vaccine Circulation and Mutation after Mexican National Immunization Weeks
Conclusion: OPV, primarily serotype 2, was detected in sewage as late as 7 months after an NIW in a Mexican community primarily vaccinated with IPV, but was not detected at 8 months, suggesting that OPV circulation may have ceased. VAPP mutants were predominantly detected. This data suggests that in communities with high vaccination rates, one or two years of IPV administration after OPV cessation could be sufficient to prevent outbreaks of paralytic poliomyelitis from vaccine-derived strains.
Polio vaccine suspected as cause of fatal mutant form of encephalitis
The polio vaccine isn’t protecting children – and, worse, it appears to be causing a new and sometimes fatal form of the disease.
Concerns about the vaccine have arisen following a high number of deaths and hospital admissions from encephalitis and polio in the Uttar Pradesh region of India – where there has been an intensive vaccination programme.
Around 400 children have died, and a further 2,300 admitted to hospital, following an outbreak of a new form of viral encephalitis, and doctors admit they do not know its cause.
Unvaccinated Blamed for Mutated Polio, (AGAIN ALWAYS FALSELY THE UNVACCINATED ARE BLAMED FOR ANYTHING THAT HAPPENS)
Mutant polio vaccine regains virulence
But the latest study raises the frightening possibility that the vaccine strain can also regain the ability to spread between people more easily than thought. “It demonstrates clearly that the vaccine virus can spread from person to person,” says Olen Kew from the Centers for Disease Control and Prevention in Atlanta, Georgia.
The outbreak was exacerbated by the fact that Haiti had relaxed its polio vaccination program more than five years earlier. “It’s a warning that you need to have good coverage to prevent vaccines from running away like this,” Kew says.
The study also shows how difficult it will be eliminate polio entirely. For this to be achieved, natural polio would first have to be wiped out through stringent use of the oral polio vaccine. Then all countries could simultaneously stop vaccinating or switch to a different vaccine – injectable, dead polio virus.
This method does not confer as much immunity as the oral vaccine, but it cannot revert to a disease-causing form. This vaccine is already used in the US and much of Europe.
This again points to the claim that they think they need to get 100% vaccine coverage in ever country with existing polio, and only then it may be possible to stop polio, but yet they know they will have the mutations still going on and the result of that is in their minds quite obviously only necessary collateral damage, so to speak. So, as long as they can keep blaming it all on the unvaccinated, which is not exactly proven; it is an assumption. And as long as they keep playing Russian Roulette with the vaccine virus; in the hopes that it does not continue to mutate to a point of becoming a super virus world wide. But in the end, the with the known odds that have been and in the resulting outcomes; clearly it all shows this plan to be not only failing and dangerous; but even currently, is likely causing more harm than good; and will continue to.
J Clin Microbiol. 1995 Sep;33(9):2485-8.
Detection of measles virus RNA in urine specimens from vaccine recipients.
Rota PA, Khan AS, Durigon E, Yuran T, Villamarzo YS, Bellini WJ.
Source: Division of Viral and Rickettsial Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia 30333, USA.
Analysis of urine specimens by using reverse transcriptase-PCR was evaluated as a rapid assay to identify individuals infected with measles virus. For the study, daily urine samples were obtained from either 15-month-old children or young adults following measles immunization. Overall, measles virus RNA was detected in 10 of 12 children during the 2-week sampling period. In some cases, measles virus RNA was detected as early as 1 day or as late as 14 days after vaccination. Measles virus RNA was also detected in the urine samples from all four of the young adults between 1 and 13 days after vaccination. This assay will enable continued studies of the shedding and transmission of measles virus and, it is hoped, will provide a rapid means to identify measles infection, especially in mild or asymptomatic cases.
You see in the next below link that it ALL depends on who has done the study, as for if they find the evidence of shedding due to a/or the vaccine. Here we have the Journal of Infectious diseases that is closely aligned with pharma and Offit’s CHOP. And they of course find predicable no shedding. Can you imagine the upset if they had, and presented to the CDC with that? Clearly, is not happening.
J Infect Dis. 2004 May 1;189 Suppl 1:S165-70.
Lack of evidence of measles virus shedding in people with inapparent measles virus infections.
And here, and again pharma connected
So, the pro vaccine side again claims to what? Well if there are no studies to prove that the vaccines cause shedding, then it simply doesn’t happen. Just like in regard to the vaccine aluminum adjuvants; if no studies have ever been done, then we can proclaim that there is no scientific proof of the harm, thus there is no said harm being done.
J Clin Microbiol. 2008 Mar;46(3):1101-3. Epub 2008 Jan 9.
Detection of RNA of mumps virus during an outbreak in a population with a high level of measles, mumps, and rubella vaccine coverage.
Bitsko RH, Cortese MM, Dayan GH, Rota PA, Lowe L, Iversen SC, Bellini WJ.
Source:Epidemic Intelligence Service, Office of Workforce and Career Development, Centers for Disease Control and Prevention, Atlanta, GA 30333, USA.
The duration of mumps virus RNA detection was studied during a mumps outbreak in a highly vaccinated university population. Seven of the eight reverse transcription-PCR-positive specimens were collected during the first 3 days of parotitis, suggesting that viral shedding is minimal after the first 3 days of symptoms.
However, in three days, you could infect 100’s of people.
General Index: But as you can see, very few actual studies on vaccine shedding have been done.
Secondary Transmission: The short and sweet about live virus vaccine shedding.(A short list of the evidence of shedding in regard to each specific vaccine).
Measles Vaccine Found in Throat of Vaccinated Child
Pediatr Dermatol. 2005 Mar-Apr;22(2):130-2.
Vaccine-associated “wild-type” measles.
Acta Paediatr Jpn. 1995 Jun;37(3):374-6.
Measles encephalomyelitis in a patient with a history of vaccination.
Clin Infect Dis. 1999 Oct;29(4):855-61.
Measles inclusion-body encephalitis caused by the vaccine strain of measles virus.
Pediatr Neurol. 1999 May;20(5):399-402.
Acute disseminated encephalomyelitis with probable measles vaccine failure.
I would take my chances with natural infection and recovery, any day; over that of the use of a vaccine, or in this and the most common case, the MMR vaccine..
January 24th, 2013 | Updated 01/24/2013 at 1:28 pm
Just two days after it was reported that GlaxoSmithKline’s Pandemrix H1N1 swine flu vaccine has actually caused a whopping 800 cases of narcolepsy in children according to Reuters, a major publicity stunt for the efficacy of the flu shot as presented by CNN has crashed and burned. After receiving his very first flu shot live on air from vaccine advocate Dr. Oz in attempt to showcase the ‘safety and effectiveness of the shot’, Piers Morgan has now developed flu-like symptoms that even he and his guest have attributed to the reception of the shot.
In the January 23 interview with country music celebrity Dwight Yoakam, Piers and Dwight discuss the connection between the recent shot and his new sickness. In the interview, which can be seen below, Piers asks “…As you can tell, things are deteriorating. Is there any advice you can give me?”
Yoakam replies with a simple “Don’t ever take a flu shot again,” sparking further discussion surrounding the public injection that ultimately turned into a PR nightmare for Big Pharma. In a surprising reply, Piers says ““We’re both doing the math, so I mean, we both saw him put that thing in my arm and within 10 days I’m struck down.” It was Piers’ first flu shot in his life, according to his own testimony.
You can watch this segment below:
As pointed out by Adan Salazar, the sickness is also highly ironic as Piers actually questioned Dr. Oz about the so-called ‘myths’ surrounding the shot before it was administered. One such ‘myth’ was whether or not the shot could actually lead to the flu. In dialogue with Dr. Oz, Piers nervously asked:
“So the myth about these, and I’m told it’s a myth, is that you can actually get flu or flu-like symptoms simply by having the shot. Is that true?”
Dr. Oz, of course, regurgitated information provided by the CDC in stating that such an event is impossible due to the fact that the flu shot contains the dead flu virus. Dr. Oz also fails to mention that even the FDA’s own website admits that vaccines contain toxic additives like:
Antibiotics: Linked to the development of mental illness, obesity, and serious gut imbalance due to the depletion of beneficial bacteria in the gut, superbug-spawning antibiotics are used in vaccinations as an ‘additive’ as admitted by the FDA.
Formaldehyde: This of course is the known carcinogen used in the preservation of corpses by funeral homes and elsewhere. Even Cancer.gov admits that formaldehyde is a serious cancer-causing chemical, stating “Formaldehyde has been classified as a known human carcinogen (cancer-causing substance) by the International Agency for Research on Cancer…” So why is this cancer-causing substance being used an additive for vaccinations?
Aluminum: Popularly associated with Alzheimer’s disease and a bunch of other brain disorders, aluminum is used as a vaccine additive to ‘stimulate a response’ from the body.
Thimerosal: One of the most widely known additives, thimerosal is a mercury-containing substance that is unsafe at any dose. Your doctor is likely entirely misinformed on this additive, stating there is no mercury-containing thimerosal in a vaccine when even the FDA and CDC plainly state this. As stated by Dr. David Wallinga from the Institute for Agriculture and Trade Policy, mercury is ‘toxic in all its forms.”
Instead of giving Piers a vaccination full of these toxic additives, Dr. Oz could have simply recommended that Piers begin supplementing with high quality, inexpensive vitamin D3 — or simply take a walk around outside in a warmer climate. Even in considerably low doses, vitamin D3 has been found to flash the risk of flu development by nearly half – a much great success rate than the flu shot.
The federal Vaccine Injury Compensation Program, better known as “vaccine court,” has just awarded millions of dollars to two children with autism for “pain and suffering” and lifelong care of their injuries, which together could cost tens of millions of dollars
The government did not admit that vaccines caused autism, at least in one of the children. Both cases were “unpublished,” meaning information is limited, and access to medical records and other exhibits is blocked. Much of the information presented here comes from documents found at the vaccine court website.
Some observers will say the vaccine-induced encephalopathy (brain disease) documented in both children is unrelated to their autism spectrum disorder (ASD). Others will say there is plenty of evidence to suggest otherwise.
What’s more, these cases fit the pattern of other petitions, (i.e., Poling and Banks) in which the court ruled (or the government conceded) that vaccines had caused encephalopathy, which in turn produced permanent injury, including symptoms of autism and ultimately an ASD diagnosis.
And most of these children now have taxpayer dollars earmarked for applied behavioral analysis (ABA), an effective therapy specifically designed to treat ASD.
Meanwhile, parents, grandparents, friends and neighbors of both children testified they were developmentally normal, if not advanced for their age when they developed seizures, spiking fevers and other adverse reactions to their vaccines. According to these eyewitnesses, the children never fully recovered, and instead began losing vocabulary, eye contact and interest in others around them, all classic symptoms of regressive autism.
In the first case, involving a 10-year-old boy from Northern California named Ryan Mojabi, the parents allege that “all the vaccinations” received from 2003-2005, and “more specifically, measles-mumps-rubella (MMR) vaccinations,” caused a “severe and debilitating injury to his brain, described as Autism Spectrum Disorder (‘ASD’).”
The parents, who did not want to be interviewed, specifically asserted that Ryan “suffered a Vaccine Table Injury, namely, an encephalopathy” as a result of his MMR vaccination on December 19, 2003.” (“Table injuries” are known, compensable adverse reactions to immunizations.)
Alternatively, they claim that “as a cumulative result of his receipt of each and every vaccination between March 25, 2003 and February 22, 2005, Ryan has suffered . . . neuroimmunologically mediated dysfunctions in the form of asthma and ASD.”
In vaccine court, the U.S. Department of Health and Human Services acts as the defendant and Justice Department attorneys act as counsel.
In 2009, Ryan’s case was transferred to vaccine court’s Autism Omnibus Proceedings, according to the docket. A year-and-a-half later, the government conceded that MMR vaccine had indeed caused Ryan’s encephalopathy.
HHS agreed that “Ryan suffered a Table injury under the Vaccine Act — namely, an encephalitis within five to fifteen days following receipt,” of MMR, records show. “This case is appropriate for compensation.”
Whether HHS agreed with Ryan’s parents that his vaccine-induced brain disease led to ASD is unknown. The concession document is under seal.
In December 2003, when Ryan was nearly two, he received his first MMR and hepatitis B vaccines before his family left for an extended trip overseas. That day, his mother testified, Ryan began shaking with uncontrollable tremors and “was really uncomfortable, he didn’t feel well at all.”
The nurse at Ryan’s pediatrician said the symptoms were “pretty normal after the vaccination,” and advised Tylenol. The next day, Ryan began crying, “but it’s not a normal crying,” his mother testified. “He didn’t go to sleep, he was without energy.”
The family considered postponing their holiday, but that wasn’t feasible. The doctor’s office said it was fine to travel. Prior to leaving, Ryan’s mother said, the boy had difficulty breathing and “was without energy and sleepy.” He could no longer hold his head up, something “he could do prior to the vaccinations.” At the airport, Ryan began “screaming,” she recalled. “He was just opening and closing his eyes so hard, he was pulling my hair.”
After his shots, she added, Ryan “stopped saying those words that he had, even mommy and daddy, that he had repeated a hundred times before.”
In early January, while still abroad, Ryan was rushed to the hospital with vomiting, high fever and red spots covering his body “from head to toe in a measles-like rash,” the attending physician said. Ryan was diagnosed with “febrile convulsion, probably related to MMR.”
The next day, another doctor diagnosed him with “high fever, skin rash, tremors, and lethargy,” which were “most likely due to an adverse reaction to multiple vaccines he received earlier.”
Two days later, Ryan returned to the hospital with a persistent fever of 104 or more.
Ryan’s parents testified that, upon returning home, they expressed worry to their pediatrician about behavioral problems, non-responsiveness and language loss, which later produced an ASD diagnosis.
At trial, however, the government argued powerfully that written medical records, and the recollections of Ryan’s doctor, were inconsistent with his parents’ testimony. If Ryan had truly suffered an MMR encephalopathy, for example, his family would never have taken him overseas. And his parents’ complaints of ASD symptoms were raised a full year after returning from abroad, they alleged. It looked like the family had a weak case.
But then something changed.
In October, 2010, Ryan’s attorney filed four new exhibits (under seal) and proposed amending the court’s “findings of fact.” In January and May of 2011, several more exhibits were filed, along with a motion to further supplement the findings of fact.
A month later HHS conceded the case, which moved into the damages phase.
Award details were announced a few days ago: A lump sum of $969,474.91, to cover “lost future earnings ($648,132.74), pain and suffering ($202,040.17), and life care expenses for Year One ($119,302.00),” plus $20,000 for past expenses.
Another undisclosed sum, several millions more, will be invested in annuities to cover yearly costs for life, which could total $10 million or more, not accounting for inflation. Nearly $80,000 was earmarked for ABA in the first two years.
The second case involves a girl named Emily, whose mother, Jillian Moller, filed back in 2003 and has been fighting in vaccine court since. The docket, crammed with 188 items, documents Moller’s extended but victorious struggle to win compensation for Emily, who has seizure disorder and PDD-NOS, a form of ASD.
Moller alleged that Emily was severely injured by a reaction to the DTaP vaccine at 15 months (when MMR, HiB and Prevnar were also given). “She had a vaccine reaction and she just spiraled out of control,” Moller said in an interview.
Emily’s fever spiked to 105.7 and she began screaming. She stared blankly and developed seizures. Before long she began “shaking episodes” at night and “repetitive behaviors, including arm flapping and spinning,” court documents show. Like Ryan, she developed a measles-type rash.
Things went from bad to worse. Emily’s medical record is filled with damage and suffering. One neurologist, for example, noted that Emily “had staring spells and an abnormal EEG.” Another diagnosed “encephalopathy characterized by speech delay and probable global developmental delay that occurred in the setting of temporal association with immunizations as an acute encephalopathy.”
Moller filed for an encephalopathy Table injury in 2003, unaware her daughter would be diagnosed with ASD.
Two hearings were held in 2005. “I was badgered and harassed for four hours on the stand,” she said. “They said Emily couldn’t have been that sick, or else I would’ve taken her to the ER. But I took her to my doctor and he said not to bring her to the hospital!”
Government lawyers insisted that Emily had suffered neither a vaccine injury nor encephalopathy. But every alternative cause they suggested “made no sense, because she showed no signs of those things before that vaccination,” Moller said.
The case dragged on for years, with motions and counter-motions, status reports and expert medical reports. In 2007, Moller filed for summary judgment. That also took years, as more medical records were submitted to bolster Emily’s case.
After the ASD diagnosis, the judge reportedly became convinced that Emily would prevail. “My attorney said she was angry, she felt forced into a corner with no choice but to find for us,” Moller said. “She said, ‘Emily has autism, and I don’t want to give other families who filed autism claims any hope.'”
The government agreed to settle. Last spring the case went into mediation and, on December 3 HHS made its proffer, which was entered into the record on the 28th. Emily was awarded a lump sum of $1,030,314.22 “for lost future earnings ($739,989.57), pain and suffering ($170,499.77) and life care expenses for Year One ($119,874.88) plus $190,165.40 for past expenses.” Some of that money will go to ABA therapy.
Based on the first year payout, another estimated $9 million will buy annuities for annual expenses through life, which after inflation has the potential to pay over $50 million dollars.
HHS did not admit that vaccination caused encephalopathy or autism, but merely decided not to dedicate more resources to defending the case.
“I don’t understand why they fought so hard,” Moller said. “We had the evidence: the EEG, the MRI, everything was consistent with encephalopathy, post-vaccination. How can government attorneys claim what our doctors said happened, didn’t happen?”
Perhaps the feds were loath to concede yet another vaccine case involving autism. Four cases in the Autism Omnibus Proceedings were recently compensated. Three of those cases are marked with asterisks, indicating the government did not conclude that autism can be caused by vaccines. But the fourth autism case that was paid out in 2013 (Ryan’s case? We don’t know) has no such caveat.
As for Emily, she is “not too good,” Moller said. “Her emotional state is fragile, at best. She has seizure problems and autoimmune issues… And it’s a constant fight when you have a vaccine-injured child. It’s not just the disability, it’s the ignorance. The hatred from the medical community towards families like ours is intense.”
Meanwhile, as HHS says it “has never concluded in any case that autism was caused by vaccination,” it is still underwriting autism treatments such as ABA for children in its vaccine-injury program.
Measles vaccine introduction
Measles vaccination in the US and many other countries started in the early 1960s, at the time when measles was naturally abating and was heading for the 18 year low. That’s why the vaccine seemingly lowered the incidence; however, this was only coincidental with the natural dynamics of measles.
Image from healthsentinel.com – Click image to enlarge.
As one of many examples involving all infectious diseases of childhood against which vaccines have been developed, ever since any measles vaccines have been introduced and used in mass proportions, reports of outbreaks and epidemics of measles in even 100% vaccinated populations started filling pages in medical journals.
Reports of serious reactions including deaths also appeared with increasing frequency. They are the subject of a separate essay.
Atypical measles – a new phenomenon only in the vaccinated
It is less well known to the general public that vaccinated children started developing an especially vicious form of measles, due to the altered host immune response caused by the deleterious effect of the measles vaccines. It resisted all orthodox treatment and carried a high mortality rate.
It has become known as atypical measles. (AMS)
Rauh and Schmidt (1965) described nine cases of AMS which occurred in 1963 during a measles epidemic in Cincinnati. The authors followed 386 children who had received three doses of killed measles virus vaccine in 1961. Of these 386 children, 125 had been exposed to measles and 54 developed it [i.e. measles].
The new, atypical measles, occurring in the vaccinated was characterised by high fever, unusual rash and pneumonia, often with history of vaccination with killed measles vaccine.
Rauh and Schmidt (1965) concluded that, “It is obvious that three injections of killed vaccine had not protected a large percentage of children against measles when exposed within a period of two-and-a-half years after immunization”.
Fulginiti (1967) also described the occurrence of atypical measles in ten children who had received inactivated (killed) measles virus vaccine five to six years previously.
Nichols (1979) wrote that atypical measles is generally thought to be a hypersensitivity response to natural measles infection in individuals who have previously received killed measles vaccine, although several investigators have reported AMS-like illness in children who had been vaccinated only with live measles vaccine.
He wrote that during a measles epidemic in 1974-1975 in Northern California, a number of physicians reported laboratory-confirmed measles in patients who had signs and symptoms, compatible with AMS…”We developed case criteria on the basis of serology and rash distribution and morphology. In typical measles a maculopapular rash occurs first at the hairline, progresses caudally, is concentrated on the face and trunk, and is often accompanied by Koplik’s spots. In AMS the rash Is morphologically a mixture of maculopapular, petechial, vesicular, and urticarial components. It usually begins and is concentrated primarily on the extremities, progresses cephalad, and is not accompanied by Koplik’s spots. Cases were classified as AMS if patients had 1) a rash with the distribution and morphology characteristic of AMS, and 2) a fourfold or greater rise in titer of complement-fixing measles antibody or a convalescent titer of 256”.
Continuing measles outbreaks signal increasing incidence comparable with the prevaccine era.
In the meantime, outbreaks of measles in vaccinated children have continued and intensified to this day. Contemporary observations of the ineffectiveness of vaccination indicate to me that the incidence of measles has increased and has not continued decreasing as it did for some 100 years before any type of measles vaccination was introduced.
Conrad et al. (1971) published about the dynamics of measles in the US in the last four years and conceded that measles was on the increase and that “eradication, if possible, now seems far in the future”.
Barratta et al. (1970) investigated an outbreak in Florida from December 1968 to February 1969 and found little difference in the incidence of measles in vaccinated and unvaccinated children.
Right through the 1980s, measles outbreaks in fully vaccinated children have continued all over the US and all other countries with high vaccination rates all over the world.
Robertson et al. (1992) wrote that in 1985 and 1986. 152 measles outbreaks in US school-age children occurred among persons who had previously received measles vaccine. “Every 2-3 years, there is an upsurge of measles irrespective of vaccination compliance”.
To cap it all: the largely unvaccinated Amish (they claim religious exemption) had not reported a single case of measles between 1970 and December 1987, for 18 years (Sutter et al. 1991). It is quite likely that a similar situation would have applied to outside communities without any vaccination and that measles vaccination had actually kept measles alive and kicking. According to Hedrich (1933), there is a variety of dynamics of measles occurrence, from 2-3 years to up to 18 years, as later also witnessed by the unvaccinated Amish.
Unfounded optimism for measles eradication in the US by 1 October 1982
Despite the obvious lack of success with measles vaccination, in October 1978, the Secretary of the Department of Health, Joseph A Califano Jr. announced, “We are launching an effort that seeks to free the United States from measles by 1 October 1982″.
Predictably, this unrealistic plan fell flatly on its face: after 1982 the US was hit repeatedly by major and even more sustained epidemics of measles, mostly in fully vaccinated populations. First, the blame was laid upon the “ineffective, formalin-inactivated (‘killed’) measles vaccine, administered to hundreds of thousands of children from 1963 to 1967″. However, outbreaks and epidemics of measles continued occurring even when this first vaccine was replaced with two doses of ‘live’ measles virus vaccines and the age of administration was changed.
These warnings have not been heeded. As the Swiss doctors wrote (Albonico et al. 1990), “we have lost the common sense and wisdom that used to prevail in the approach to childhood diseases. Too often, instead of reinforcing the organism’s defences, fever and symptoms are relentlessly suppressed. This is not always without consequences”.
Destruction of transplacentally-transmitted immunity by vaccination
Many researchers warned straight after the introduction of measles vaccine in the US that the generations of children born to mothers who were vaccinated in childhood will be born with poor or no transplacentally-transmitted immunity and will contract measles and other diseases too early in life.
Lennon and Black (1986) demonstrated that “haemaglutinin-inhibiting and neutralizing antibody titers are lower in women young enough to have been immunized by vaccination than older women”. The same applied to whooping cough. It explains why so many babies before vaccination age develop these diseases, and most particularly the much publicised whooping cough.
About the author
Dr Viera Scheibner is Principal Research Scientist (Retired) with a doctorate in Natural Sciences from Comenius University in Bratislava. After an eminent scientific career in micropalaeontology during which she published 3 books and some 90 scientific papers in refereed scientific journals in Australia and overseas, she studied babies’ breathing patterns with the Cotwatch breathing monitor developed by her late husband Leif Karlsson in the mid 1980s. Babies had alarms after vaccination, indicating stress. This introduced her to the subject of vaccination. She then started systematically studying orthodox medical papers dealing with vaccination issues. To this day she has collected and studied more than 100000 pages of medical papers.
Despite such extensive research of orthodox medical papers published on vaccines over the past 100 years, she established that there is no scientific evidence that these injections of highly noxious substances prevent diseases, quite to the contrary, that they increase susceptibility to the diseases which the vaccines are supposed to prevent and also to a host of related and unrelated viral and bacterial infections. Vaccines are involved in a great number of modern ills of childhood such as immunoreactive diseases (asthma, allergies), autoimmune diseases (diabetes, multiple sclerosis, lupus erythematosis), cancers, leukaemia, degenerative diseases of bone and cartilage, behavioural and learning problems, to mention just the most important conditions.
Her research into vaccination has culminated so far in two books and a number of shorter and longer individual papers published in a variety of scientific and medical publications. She has also conducted frequent international lecture tours to present the results of her research to parents, health and medical professionals and anyone else who is interested. She has also provided a great number of expert witness reports for court cases relating to deaths and injuries caused by vaccines, such as so-called “shaken baby” syndrome.
Vaccinated Children Have More Than Twice the Diseases and Disorders Than Unvaccinated Children
This survey was A German study released in September 2011 of about 8000 UNVACCINATED children, newborn to 19 years, show vaccinated children have more than twice the diseases and disorders than unvaccinated children.
The results are presented in the bar chart below; the complete data and study results are here. The data is compared to the national German KIGGS health study of the children in the general population. Most of the respondents to the survey were from the U.S. (Click on the chart to see it better)
Results: of 1004 unvaccinated children, had
Asthma, 0% (8-12% in the normal population)
A-topic dermatitis 1.2% (10-20% in the normal population)
Allergies 3% (25% in the normal population)
ADHD 0.79% (5-10%) in children
Longterm Study in Guinea-Bissau (1 Kristensen I, Aaby P, Jensen H.:“Routine vaccinations and child survival: follow up study in Guinea-Bissau, West Africa”, BMJ 2000; 321: 1435–41)
The children of 15,000 mothers were observed from 1990 to 1996 for 5 years.
Result: the death rate in vaccinated children against diphtheria, tetanus and whooping cough is twice as high as the unvaccinated children (10.5% versus 4.7%).
New Zealand Survey (1992) (http://www.ias.org.nz)
The study involved 254 children. In which 133 children were vaccinated and 121 remained unvaccinated.
|Asthma||20 (15%)||4 (3%)|
|Eczema or allergic rashes||43 (32%)||16 (13%)|
|Chronic otitis||26 (20%)||8 (7%)|
|Recurrent tonsillitis||11 (8%)||3 (2%)|
|Shortness of breath and sudden infant death syndrome||9 (7%)||2 (2%)|
|Hyperactivity||10 (8%)||1 (1%)|
Download and read the IAS1992study now.