They do make a lot of money for their makers though...
By Dr. Mercola
In the wake of Robert F. Kennedy Jr. telling reporters that President Trump asked him to chair a commission on vaccine safety and scientific integrity, the media is angling to shame and ridicule vaccine safety and informed consent proponents, be they physicians, scientists or parents with the ability to read and think for themselves.
Although Kennedy's appointment has not been confirmed yet by the Trump administration, The Atlantic has gone so far as to suggest that a "shadow network of anti-vax doctors" is being emboldened by questions and concerns the new president has voiced about vaccine safety.1
Like Kennedy and many other critics of vaccine science and policy, President Trump has been outspoken about his suspicions that vaccines and vaccine policies may not be nearly as safe as they're portrayed, and that the science is far from settled.
Meanwhile, Kennedy recently co-wrote an article in which he released documents revealing that officials at the Food and Drug Administration (FDA) and Centers for Disease Control and Prevention (CDC) "knew that infant vaccines were exposing American children to mercury far in excess of all federal safety guidelines since 1999."2
Recent reports also reveal that medical treatment guidelines are frequently influenced by drug industry ties,3 and scientific "citation cartels" are gaming the system by repeatedly citing each other's work,4 thereby making their studies appear more noteworthy and establishing what amounts to a false base of research that becomes difficult to overturn by independent researchers.
In all, there can be little doubt that the drug industry is getting anxious and this is why the heat is being turned up against anyone daring to question the status quo on vaccines.
Clearly, having an open discussion about vaccine safety means opening the door to doubt, and this is something the drug industry simply cannot afford. Meanwhile, avoiding the discussion is something parents, and the health care system as a whole, can no longer afford.
Documents Reveal Government Betrayal
In his article, Kennedy claims that documentation8 obtained via FOIA proves the FDA and CDC knew childhood vaccines were overexposing children to mercury, which is a well-known potent neurotoxin.
Part of the FDA Modernization Act, passed by Congress in 1997, required the FDA to compile a list of pharmaceutical products that contain mercury.
More than 30 FDA licensed inactivated vaccines containing the mercury-based preservative, thimerosal, ended up on this list and included DPT/DTaP, HIB and hepatitis vaccines routinely given to babies between day of birth and 18 months old.
The FDA was also charged with conducting a quantitative and qualitative analysis of the mercury compounds on the list. This responsibility fell on the FDA's Center for Biologics Evaluation and Research (CBER).
Prior to this, no one had ever added up the cumulative mercury exposure resulting from thimerosal-containing infant vaccines. According to Kennedy:9
By Dr. Mercola
In the wake of Robert F. Kennedy Jr. telling reporters that President Trump asked him to chair a commission on vaccine safety and scientific integrity, the media is angling to shame and ridicule vaccine safety and informed consent proponents, be they physicians, scientists or parents with the ability to read and think for themselves.
Although Kennedy's appointment has not been confirmed yet by the Trump administration, The Atlantic has gone so far as to suggest that a "shadow network of anti-vax doctors" is being emboldened by questions and concerns the new president has voiced about vaccine safety.1
Like Kennedy and many other critics of vaccine science and policy, President Trump has been outspoken about his suspicions that vaccines and vaccine policies may not be nearly as safe as they're portrayed, and that the science is far from settled.
Meanwhile, Kennedy recently co-wrote an article in which he released documents revealing that officials at the Food and Drug Administration (FDA) and Centers for Disease Control and Prevention (CDC) "knew that infant vaccines were exposing American children to mercury far in excess of all federal safety guidelines since 1999."2
Recent reports also reveal that medical treatment guidelines are frequently influenced by drug industry ties,3 and scientific "citation cartels" are gaming the system by repeatedly citing each other's work,4 thereby making their studies appear more noteworthy and establishing what amounts to a false base of research that becomes difficult to overturn by independent researchers.
In all, there can be little doubt that the drug industry is getting anxious and this is why the heat is being turned up against anyone daring to question the status quo on vaccines.
Clearly, having an open discussion about vaccine safety means opening the door to doubt, and this is something the drug industry simply cannot afford. Meanwhile, avoiding the discussion is something parents, and the health care system as a whole, can no longer afford.
Documents Reveal Government Betrayal
In his article, Kennedy claims that documentation8 obtained via FOIA proves the FDA and CDC knew childhood vaccines were overexposing children to mercury, which is a well-known potent neurotoxin.
Part of the FDA Modernization Act, passed by Congress in 1997, required the FDA to compile a list of pharmaceutical products that contain mercury.
More than 30 FDA licensed inactivated vaccines containing the mercury-based preservative, thimerosal, ended up on this list and included DPT/DTaP, HIB and hepatitis vaccines routinely given to babies between day of birth and 18 months old.
The FDA was also charged with conducting a quantitative and qualitative analysis of the mercury compounds on the list. This responsibility fell on the FDA's Center for Biologics Evaluation and Research (CBER).
Prior to this, no one had ever added up the cumulative mercury exposure resulting from thimerosal-containing infant vaccines. According to Kennedy:9
"When the agency finally performed that basic calculation, the regulators realized that a [6]-month-old infant who received thimerosal-preserved vaccines following the recommended CDC vaccine schedule would have received a jaw dropping 187.5 micrograms of mercury.
Instead of immediately ordering the removal of thimerosal, FDA officials circled the wagons treating the public health emergency as a public relations problem. Peter Patriarca, then director of the FDA Division of Viral Products, warned his fellow bureaucrats that hasty removal of thimerosal from vaccines would:
'… raise questions about FDA being 'asleep at the switch' for decades by allowing a potentially hazardous compound to remain in many childhood vaccines, and not forcing manufacturers to exclude it from new products.
It will also raise questions about various advisory bodies regarding aggressive recommendations for use. We must keep in mind that the dose of ethylmercury was not generated by "rocket science."
Conversion of the percentage thimerosal to actual micrograms of mercury involves ninth grade algebra. What took the FDA so long to do the calculations? Why didn't CDC and the advisory bodies do these calculations when they rapidly expanded the childhood immunization schedule?'
Toxicology Models Confirm Mercury Overexposure
Dr. Barry Rumack was one of the consultants hired by the FDA to delve deeper into the cumulative mercury exposure problem from vaccines given to babies in the first few years of life. In 1999, Rumack presented a model of the mercury blood-and-body burden associated with childhood vaccines, showing that:
The agency that is supposed to protect the public from unsafe pharmaceutical products concealed these alarming findings about "bolus" (large amount) mercury exposures to infants receiving multiple thimerosal-containing vaccines simultaneously by using a statistical trick in which they simply averaged the mercury exposure over a period of six months.
In reality, the bolus mercury exposures via multiple vaccines given on a single day occurred at four specific times during the first year of a child's life: at birth, and at 2, 4 and 6 months of age. By averaging the exposures over the full six months, the spikes in mercury on the four days of vaccination disappeared. According to Kennedy:
Using this statistical trickery, mercury levels from childhood vaccinations ended up being lower than FDA and ATSDR guidelines, leading the Public Health Service and the American Academy of Pediatrics to report that:
Remarkably, even with this statistical trick, "The levels were still above EPA guidelines which were the most stringent of the three,"
Kennedy writes,10 adding that "Numerous toxicologists have reported that the FDA's calculation, averaging these high bolus dose exposures, was not appropriate." Moreover, it appears the FDA may have misguided the pediatrician, Dr. Leslie Ball, assigned to oversee the public reporting of the ATSDR results.
According to Kennedy, Ball was unfamiliar with toxicology and, when confronted about the statistical manipulation, she replied that she was basically just following orders, saying, "That is what I was told to do." Email correspondence from 1999 shows that even Ball herself questioned the rationale behind averaging the exposures. In a July, 1999 email to Norman Baylor, Ph.D., director of the Office of Vaccines Research Review, marked "confidential," Ball asked:11
Kennedy has also reported that the CDC owns more than 20 different vaccine patents and sells $4.1 billion in vaccines each year, noting that those patents create a significant undisclosed conflict of interest when it comes to the agency's involvement in vaccine safety.12
Mark Blaxill, who specializes in intellectual property law, in 2010 wrote about the fact that the U.S. Department of Health and Human Services (DHHS), through the National Institutes of Health (NIH), holds patent rights to the HPV vaccines Gardasil and Cervarix, and receives a percentage of the profits from the administration of these vaccines on a global scale.13"
Toxicology Models Confirm Mercury Overexposure
Dr. Barry Rumack was one of the consultants hired by the FDA to delve deeper into the cumulative mercury exposure problem from vaccines given to babies in the first few years of life. In 1999, Rumack presented a model of the mercury blood-and-body burden associated with childhood vaccines, showing that:
"… [T]himerosal-containing vaccines was dosing American children with mercury levels far exceeding all three federal safety guidelines established by the U.S. Environmental Protection Agency (EPA), FDA and Agency for Toxic Substances and Disease Registry (ATSDR)," Kennedy writes.
"There was no point in time from birth to approximately 16-18 months of age that infants were below the EPA guidelines for allowable mercury exposure. In fact, according to the models, blood-and-body burden levels of mercury peaked at [6] months of age at a shockingly high level of 120ng/liter. To put this in perspective, the CDC classifies mercury poisoning as blood levels of mercury greater than 10 ng/L."
With the certain knowledge that infants were being exposed to unacceptably high mercury burdens through vaccines, what the FDA did next is unforgivable.
The agency that is supposed to protect the public from unsafe pharmaceutical products concealed these alarming findings about "bolus" (large amount) mercury exposures to infants receiving multiple thimerosal-containing vaccines simultaneously by using a statistical trick in which they simply averaged the mercury exposure over a period of six months.
In reality, the bolus mercury exposures via multiple vaccines given on a single day occurred at four specific times during the first year of a child's life: at birth, and at 2, 4 and 6 months of age. By averaging the exposures over the full six months, the spikes in mercury on the four days of vaccination disappeared. According to Kennedy:
"An analogy would be to compare taking two Tylenol tablets a day for a month to taking 60 Tylenol tablets in one day; the first exposure is acceptable, while the other is lethal."
Even With Deception, Mercury Burden Exceeded EPA Guidelines
Using this statistical trickery, mercury levels from childhood vaccinations ended up being lower than FDA and ATSDR guidelines, leading the Public Health Service and the American Academy of Pediatrics to report that:
"There is a significant safety margin incorporated into all the acceptable mercury exposure limits. Furthermore, there are no data or evidence of any harm caused by the level of exposure that some children may have encountered in following the existing immunization schedule. Infants and children who have received thimerosal-containing vaccines do not need to be tested for mercury exposure."
It would seem the last sentence was added as a protective buffer to prevent people from actually conducting further testing of actual mercury levels in children following repeated injections with mercury-containing vaccines in the first few years of life.
Remarkably, even with this statistical trick, "The levels were still above EPA guidelines which were the most stringent of the three,"
Kennedy writes,10 adding that "Numerous toxicologists have reported that the FDA's calculation, averaging these high bolus dose exposures, was not appropriate." Moreover, it appears the FDA may have misguided the pediatrician, Dr. Leslie Ball, assigned to oversee the public reporting of the ATSDR results.
According to Kennedy, Ball was unfamiliar with toxicology and, when confronted about the statistical manipulation, she replied that she was basically just following orders, saying, "That is what I was told to do." Email correspondence from 1999 shows that even Ball herself questioned the rationale behind averaging the exposures. In a July, 1999 email to Norman Baylor, Ph.D., director of the Office of Vaccines Research Review, marked "confidential," Ball asked:11
"Has the application of these calculations as exposure guidelines received the sign off by toxicologists? In prior discussions, the toxicologists seemed reluctant to state any Hg (mercury) level was 'safe.'"
CDC Vaccine Patents Create Serious Conflicts of Interest
Kennedy has also reported that the CDC owns more than 20 different vaccine patents and sells $4.1 billion in vaccines each year, noting that those patents create a significant undisclosed conflict of interest when it comes to the agency's involvement in vaccine safety.12
Mark Blaxill, who specializes in intellectual property law, in 2010 wrote about the fact that the U.S. Department of Health and Human Services (DHHS), through the National Institutes of Health (NIH), holds patent rights to the HPV vaccines Gardasil and Cervarix, and receives a percentage of the profits from the administration of these vaccines on a global scale.13"
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