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“The concern scientists had regarding passenger viruses was not unfounded. You may recall the disastrous SV40 monkey virus which contaminated the polio vaccines. There are scientists who claim this virus is the cause of multiple human cancers. On CDC’s website a page on vaccine safety, which was suddenly removed (archived copies exist), states that: “SV40 virus has been found in certain types of cancer in humans, but it has not been determined that SV40 causes these cancers.”

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“Perhaps there is something within the genetic make-up of specific individuals which predisposes them to accumulate and retain aluminium in their brain, as is similarly suggested for individuals with familial Alzheimer’s disease. The new evidence strongly suggests that aluminium is entering the brain in ASD via pro-inflammatory cells which have become loaded up with aluminium in the blood and/or lymph, much as has been demonstrated for monocytes at injection sites for vaccines including aluminium adjuvants. Perhaps we now have the putative link between vaccination and ASD, the link being the inclusion of an aluminium adjuvant in the vaccine.”

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“In vaccine trials the placebo for the control group is often an aluminum-containing vaccine. That fact alone could account for why so many mainstream-approved research studies have inconclusive and perhaps even contradictory outcomes.”

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“Another way is via genetic engineering. Here the germ is inserted into plasmid that has been manipulated by scientists. This type of plasmid is circular segments of DNA extracted from bacteria to serve as a vector. Scientists can add multiple genes and whatever genes they want into this plasmid. In case of vaccines, this includes a genetic piece of the vaccine germ and normally a gene for antibiotic resistance. This means that when the toxic gene is cultured inside the yeast, it has been designed with a new genetic code that makes it resistant to the antibiotic it’s coded for. The gene-plasmid combo is inserted into a yeast cell to be replicated. When the yeast replicates, the DNA from the plasmid is reproduced as a part of the yeast DNA. Once enough cells have been replicated, the genetic material in the new and improved yeast cell is extracted and put into the vaccine. Examples of this vaccine are the acellular pertussis and hepatitis B vaccines. One thing that doesn’t seem to concern scientists is the fact that the manmade genetic combination becomes the vaccine component. This mixture of intended and unintended genetic information may cause our immune system to overreact. This can be especially complicated for a child with compromised immune system. Another concern is that this new genetic code can become integrated with our own genetic material. Yeast, for instance, is very much like human DNA. It shares about one third of our proteins.”

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“Experimental research, however, clearly shows that aluminum adjuvants have a potential to induce serious immunological disorders in humans. In particular, aluminum in adjuvant form carries a risk for autoimmunity, long-term brain inflammation and associated neurological complications […].”[109]”

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“To cover as many of these (childhood vaccines) as possible, we have decided to use the vaccines on the US childhood schedule of the Center for Disease Control and Prevention (CDC). This schedule, as far as we can tell, includes more vaccines than any other country in the world.”

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“We have phosphate on our DNA. Aluminum attaches itself to it and messes up our genetic coding process. While the aluminum is inside a cell, some of its particles attach to adenosine triphosphate (ATP). The ATP is in charge of our cell’s energy production. So, in this manner the aluminum can affect our energy level. We have enzymes (proteins) within our cells that depend on attaching themselves to calcium (Ca) or magnesium (Mg) to function properly. Once our enzymes have attached to the Ca and Mg, they can carry on with their functions. Because the aluminum has such a strong positive charge, it’s able to break the bond between our enzymes and Ca or Mg. These enzymes are now no longer attached to Ca or Mg. They have become neutralized and are unable to carry out their responsibilities. We need these enzymes for efficient metabolism, but now the aluminum is attached to the enzymes instead. The protein molecules all look a little different because their shape reflects what they are designed to do. Aluminum disturbs their individual tasks and clumps them together so they are now misshapen and no longer functioning. Aluminum also messes with the cell surface, the membrane, the outer layer of the cell. With a dysfunctional cell membrane, everything inside the cell becomes compromised and it is no longer able to properly communicate with the environment surrounding the cell about what needs to be done[96].”

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“It’s very important the person being vaccinated has healthy kidneys as they are a vital part of eliminating aluminum (Al) from the blood. We wonder if many doctors test infants and children for healthy kidneys before vaccinating them. A good test for this would be to check the Glomerular Filtration Rate (GFR)[105]. This tells us how well the kidneys (glomerulus) are filtering the blood. To know how much aluminum the kidneys can handle, we must know their GFR.”

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“They also observed that the amygdala in the vaccinated monkeys didn’t mature with time as it was supposed to. The amygdala, incidentally, plays an important role in social interactions. Maybe it’s not so surprising they also observed that in the vaccinated monkeys the opioid antagonist diprenorphine (DPN) levels never lowered throughout the study. In the placebo group, the DPN levels decreased noticeably. One function of DPN is to block social interaction. What this means is the research showed that the social behavior of those monkeys that received the actual vaccines, where the DPN levels did not decrease, turned anti-social. We found there was at least one more study undertaken to verify the association between DPN and social behavior. Performed in 1981[141]. The authors of that study believe the release of opioids in the brain encourages social interactions. So, when the body fails to decrease the amount of the antagonist DPN, it not only blocks the opioids that encourage social interactions, but it blocks the desire to socially interact.”

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“A study we came across revealed that p80 is very efficient at removing mercury from contaminated water[245]. This sounds good right? Read on… If p80 is attracting mercury, we can only assume it is likely some of the mercury is being escorted to the brain. So, if we receive traces of mercury in the vaccines or are exposed to mercury from other sources, and receive a p80 containing vaccine, then a mercury-free vaccine could still potentially cause mercury accumulation in the brain.”

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