Vaccine News – 13 Year-Old Boy Permanently Disabled from Chicken Pox Vaccine Wins His Case in Vaccine Court – Eyes wide open yet?

The Amazing Dr. Franz from Orlando.
#gooddoctor #pediatrician #vaxxed #praybig #VaxxedDoctors

#VaxXed #PanRan2 #HepB #PanRan Again
Vaxxed team at Pan’s hep B meeting Aug. 9 at the capitol
https://www.periscope.tv/AutismMedia/1mnGekQVrpZxX?
https://www.youtube.com/watch?v=o6SFxxap6qc

A legal process has been initiated for a 5 year moratorium on childhood vaccines until tests can be conducted. This is not merely an internet petition, or a White House petition (although one has been started) but the beginning of a basis to take legal action — and we have a sympathetic ear in President Trump.
Full video to share with those not on Facebook – youtube.com/watch?v=rjGKqPoaS_w
#VaccineMoratorium #RevolutionForChoice #InformedConsent #Vaxxed #HearThisWell
Vaxxed – A Revolution For Choice

How will it end? What pivotal event will historians point to and say that was the day the madness ended? I think I know.
This is a studio version of a talk I gave at the CDCTruth event in Atlanta on October 15, 2016.
Shares work better than likes!

237 deaths by Pentavalent vaccine and still counting
By JACOB PULIYEL | NEW DELHI | 13 November, 2016
Under Right to Information we know that up to August 2016 there have been 237 deaths reported to the government here within 72 hours of vaccination with Pentavalent. We examined deaths in states which were giving DPT and Pentavalent vaccine concurrently.
There were three deaths following the use of Pentavalent vaccine in Sri Lanka. The Government of Sri Lanka suspended the use of the vaccine. WHO experts investigated the deaths. They found there was a clear temporal association of the deaths to the vaccine (WHO terminology, meaning the deaths followed soon after vaccination) and there was no alternate explanation for the deaths. According to the standard protocol in investigation of vaccine deaths these deaths would have to be declared as “probably” caused by Pentavalent vaccine. The experts balked at the prospect of giving such a report. No country would use this vaccine after that. Instead they wrote in their report that they were deleting “probable” and “possible” from the standard classification. The report maintained that although it was probably related to vaccine, they were reporting it as “unlikely” to be related to vaccination.
The full report was not published online, only the conclusion was made public.
The full report was presented to the Delhi High Court in a vaccine case. Once this devious methodology employed by the WHO experts was known, it was exposed by the British Medical Journal.
Following the exposé, the WHO set up a 40-member committee called the CIOMS/WHO committee. 19 of the 40 were representatives of vaccine manufacturers with conflicts of interest. They developed a new algorithm for investigating adverse events after immunization, which decreed that any reaction seen first in Phase 4 trial must be ignored.
When a drug is developed it is tested in a randomised controlled trial called the Phase 3 trial. The numbers tested are limited to a few thousand. If there is no adverse reaction the drug is licensed for Phase 4 trials with it given to a larger number. Reactions that happen less than 1 in 10,000 are noticed for the first time in Phase 4 trials. If the same reaction happens repeatedly it is considered as a “signal” that the reaction is caused by the drug and studies in the community in the form of case-control investigations are done to establish if the reactions happen in the community setting.

But here are the important questions regarding HPV:
If two doses are just as effective as three, why recommend three doses in the first place, especially for a vaccine that costs $120 per dose (the highest of the childhood vaccine schedule)? And would they have discovered this error if they had completed the full four years of safety/efficacy research instead of fast-tracking the vaccine? The new schedule recommends 6 to 12 months between the two doses. Are they increasing the time between doses to reduce the number of severe neurological reactions? Couldn’t they have discovered that if they had stuck to the four-year safety study? And more concerning, could this also be true for other vaccines?
Asking questions about whether or not vaccines are truly “safe and effective” doesn’t make you anti-vaccine. You have the right to know.
In an unprecedented move last November, the CDC announced they were reducing the number of doses of recommended HPV vaccine from 3 doses to 2 AND warning doctors to wait longer before giving the second dose. The 3-dose series has been the existing recommendation for nearly a decade, and on the current CDC schedule, which advises 70 doses of vaccines for all children, the HPV vaccine is recommended for all boys and girls 11 to 18 years old.
They say the reduced recommendation is to gain better compliance, but the reality is the CDC may have been overdosing American teens by putting the first two doses too close together, triggering severe neurological and autoimmune reactions. Research has shown that most severe side effects occurred after that second dose (given only 1 month after the first). And now the CDC has found that three doses, which they had been advising for 10 years, has no better efficacy – only more side effects. Isn’t this information something that should have been discovered during initial safety testing? And is there a chance there are unnecessary doses of other vaccines on the CDC schedule that may be causing more harm with no actual benefit?

Eyes wide open yet?
This is a 3 yr. Old little boy who is having a severe reaction to the chicken pox vaccine..
He was diagnosed yesterday and the Dr. states in his discharge papers that it was caused by the vaccine. This is his 2nd reaction to a vaccine. The symptom is the blisters that you see, and are very painful and itchy. He is attending an independent private school and apparently this is required..
Do we not see something severely wrong here??

CANCER IN KIDS?!!
Cancer is now the 2nd leading cause of DEATH in children.
Remember when it used to mostly affect older people. What’s going on here?
Could it be that most VACCINES contain a toxic additive called Formaldehyde that is KNOWN to cause cancer in humans when you inhale it?
Pharmaceutical companies would like you to think that when you inject it, it magically becomes “safe”. It is not safe in any amount and when injected, it’s far more potent than when inhaled. Pharma thinks we are stupid enough to believe in magic…but you are not falling for that lie, right?!!
NOT A COINCIDENCE!
#LearnTheRIsk #cancer #askWHY

Vaccine injury

13 Year-Old Boy Permanently Disabled from Chicken Pox Vaccine Wins His Case in Vaccine Court
A young man was recently awarded compensation in the United States Court of Federal Claims Vaccine Court, for injuries he sustained after being administered the hepatitis A and varicella vaccinations in 2009. After five long years of litigation, Health and Human Services (HHS), the Respondent in all vaccine injury cases, conceded that the varicella vaccination did in fact cause RD’s vaccine injury, transverse myelitis, which has left him a tetraplegic.
In November 2014, HHS conceded that the vaccination caused RD’s injuries. Even with this concession, his case continued for another year in the damages phase, during which time the parties continued to negotiate the amount of damages that RD would receive for his injuries. Although he was compensated for his suffering and injuries, the monetary award will never compensate for the lifelong effects this young man is suffering from his vaccine injury.
Five Long Years
RD was only 13 when his life changed forever. At a routine well-child visit in 2009, the doctor informed RD’s parents that he was due to receive the hepatitis A and varicella vaccinations. His parents complied with the doctor’s order and RD received the vaccinations.
RD’s mother explained that, at that time in RD’s state, only one dose of varicella vaccine was required and RD had already received one dose of that vaccine. This second dose that was administered to RD at this well visit was determined to be the cause of RD’s horrific injuries, and it was not even required for him, which his family didn’t realize until it was too late.
About 14 days later, RD began to experience excruciating pain shooting through his body along with tingling, numbness and paralysis of his limbs. After extensive testing and many invasive procedures, RD was diagnosed with transverse myelitis.

Breaking: interview with Vaxxed producer who was banned from Australia
Producer of film Vaxxed banned from Australia
by Jon Rappoport
August 9, 2017
Polly Tommey, producer of the famous documentary, Vaxxed (trailer), has been banned from Australia. If that sounds quite insane—it is.
Vaxxed has been screening across the world. It is an explosive revelation about egregious fraud at the US Centers for Disease Control (CDC).
The film focuses on the 2014 public confession of a long-time researcher at the CDC, William Thompson. Thompson admits that he and his colleagues committed a crime, by manipulating data to give the MMR vaccine a free pass, “proving” it had no connection to autism—when in fact, as Thompson states, the vaccine does raise the risk of autism in children.
Here are a few statements from the The Sydney Morning Herald’s report, headlined: “Anti-vaccination advocate ‘banned from Australia’ after documentary tour.”
“The producer Polly Tommey behind a controversial anti-vaccination film which has been touring Australia has been banned from returning to the country for three years, she claims.”
“Ms Tommey spearheaded a sold-out national roadshow of the documentary Vaxxed: From Cover-up to Catastrophe organised by the Australian Vaccinations-Skeptics Network.”
“In a video, posted to Youtube on Tuesday, Ms Tommey claimed authorities seized her phone and copied her emails as she left Australian soil to continue the New Zealand leg of the film tour.”

 

Advertisements

The researchers note that their cross-reactivity findings in mice are consistent with work conducted by Kanduc in humans, who identified considerable amino acid sequence similarity between the Gardasil vaccine antigen and a number of human proteins

Study:

The researchers note that their cross-reactivity findings in mice are consistent with work conducted by Kanduc in humans, who identified considerable amino acid sequence similarity between the Gardasil vaccine antigen and a number of human proteins. According to Kanduc, “the number of viral matches and their locations make the occurrence of side autoimmune cross-reactions in the human host following HPV16-based vaccination almost unavoidable.”
The mouse study findings also corroborate and amplify a prior case study report by Tomljenovic and Shaw describing immunohistochemical analysis of brain tissue specimens from two young women who died after receiving the Gardasil vaccine. Immunohistochemistry is a method for demonstrating the presence and location of antigens in tissue using antibodies that recognize the target antigen. In both cases, the standard autopsies had previously failed to ascertain an exact cause of death. Case 1 experienced progressively worsening neurological symptoms following her first Gardasil injection and died in her sleep six months after her third Gardasil booster. She showed no notable neuroinflammatory changes upon autopsy using an unspecified histological protocol. Case 2 developed a variety of symptoms after her first injection and died two weeks after the second booster. The autopsy report for Case 2 found cerebral changes consistent with encephalopathy and indicative of a “focally disrupted blood-brain barrier.”
The World Health Organization’s Global Advisory Committee on Vaccine Safety (GACVS) critiqued the Tomljenovic and Shaw case study but did so on the basis of several extremely careless and factually incorrect statements, as rebutted by leading scientist Sin Hang Lee of Milford Molecular Diagnostics. One of the objections of the GACVS was that there was “no evidence of inflammation on autopsy”—despite the fact that the autopsy for Case 2 found evidence of encephalopathy. In addition, Tomljenovic and Shaw point out that their fine-tuned analyses of brain tissue from the two deceased young women, unlike the autopsies, used microglia- and astroglia-specific markers that were able to identify “exceptionally intense micro- and astrogliosis in all brain tissue sections examined” from both cases. Microgliosis represents “an intense reaction… to pathogenic insults” and astrogliosis similarly occurs when the “astrocytic defense mechanisms [are] overwhelmed in pathological conditions.” This type of glial activation can produce “irreversible neurodestructive and pro-inflammatory processes in the brain,” according to Tomljenovic and Shaw.
With its triple findings from behavioral tests and serum and brain tissue analyses, the mouse study validates the case study report, which concludes that Gardasil (and Cervarix) are “inherently unsafe” for at least some individuals. Although it is clear that much more needs to be done to tease out the specific mechanisms whereby HPV (and other) vaccines and aluminum adjuvants can trigger autoimmune disease, the combined results of the carefully conducted mouse and human Gardasil studies cannot be easily dismissed. Together, the two studies’ results indicate that there is good reason to be cautious about aluminum-containing HPV vaccines—particularly now that the reformulated Gardasil-9 vaccine contains more than twice the amount of aluminum as its quadrivalent predecessor. The next time vaccine experts loudly proclaim that vaccine safety is unassailable, consider whether the researchers exhibited any genuine curiosity about adverse events to begin with. It’s not possible to find what you don’t look for.