Now we realise
what a failure, on so many levels, the MMR vaccine really is. But
what about its supposed safety?Given there has
NEVER been a genuine placebo safety trial or study performed on the MMR vaccine, it’s merely an untested human experiment. And our children are their guinea pigs.
According to the
Vaccine Adverse Event Reporting System database, in the U.S. alone and as of 2/5/19, the count of adverse events from the MMR vaccine alone was: 93,929 adverse events, 1,810 disabilities, 6,902 hospitalizations, and 463 deaths.
This is from just one vaccine in just one country!
How come we never hear about these from the mainstream media?
Keep in mind U.S. health authorities estimate that only about 1 percent of injuries from vaccines are even reported. This is despite paying out more than $4 billion via the taxpayer funded vaccine court for deaths and injuries caused by vaccines (a court established in 1986 to protect the vaccine industry from bankruptcy due to mounting vaccine court cases). And this is typical of the
blatant and entrenched scientific fraud that pharma gets away with on their protected and untested vaccine products – and which co-opted medical regulators grant approval!"As the Merck MMR whistle blower case proceeds toward a resolution that increasingly appears to spell doom for Merck’s scandal ridden MMRII blockbuster, HHS officials are scrambling to get Glaxo’s version of the MMR teed up to fill the coming vacuum.
Recap: Two senior Merck scientists, Stephen Krahling and Joan Wlochowski, filed their Federal whistleblower lawsuit in 2010 claiming Merck fraudulently added rabbit antibodies to human blood samples to gull FDA officials into believing the vaccine 95% effective and thereby win an MMR monopoly. When the scientists threatened to expose the fraud, Merck officials offered bribes, threatened them with prison and then destroyed the laboratory evidence in garbage bags.
Merck’s defective MMRII is currently causing dangerous Mumps epidemics in fully vaccinated adults across the globe. At FDA’s behest (GSK) recently published the results of US clinical trials for the hasty licensing of Glaxo’s (MMR) vaccine Priorix® (Klein et al. 2019).
Knowing that no MMR can survive safety testing against an inert placebo, FDA allowed GSK to test Priorix against Merck’s MMR II. The results were so horrifying for both vaccine formulations that Glaxo and FDA decided against publishing them in the main paper burying them instead in a supplemental table within an addendum.
The shocking results; Nearly 50% of vaccine recipients experienced adverse events within 42 days of vaccination and over 10% of these required emergency room visits. Roughly 2% of these adverse events were “serious” and 3.5% of vaccine recipients were diagnosed with a “new onset chronic disease” within 6 months of vaccination. These documented safety results are astronomically higher than the vaccine industry talking points which claim vaccine adverse events are “one-in-a-million”. They are much more in line with the results of the DHHS’s Lazarus study where 1 in 38 vaccine recipients showed an adverse reaction." – Robert F. Kennedy, Jr.
..HHS’s own documentation show, there is not a single vaccine brand routinely injected into American children between day one and 6 months of life that was licensed based on a clinical trial which included a placebo-control group..Tragically for Australian children, the same level of pharma-funded scientific fraud, endemic misinformation and regulatory agency co-option exists here in Australia too.
