“Another way is via genetic engineering. Here the germ is inserted into plasmid that has been manipulated by scientists.
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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.”―James Morcan. “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.”―James Morcan. “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 done96.”―James Morcan. “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 1981141.
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.”―James Morcan. “A study we came across revealed that p80 is very efficient at removing mercury from contaminated water245. 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.”―James Morcan. “My contribution is that if the pharmaceutical companies with the help of our federal government, legislative and judicial branches has “locked up”, 'bound', placed under martial law, our rights and freedoms to not be experimented on, to suffer treatment of unsafe medical practices and then also limit the freedom for independent thinkers and scientific research into examining the events around health disease, vaccines and medicine, then how are we going to become unbound, freed from the medically tyrant?
Is it already too late?”―Patricia Jordan. Clarke's research into the problems of childhood vaccines, came across the evidence that all vaccines given over a short period of time to an immature immune system deplete the thymus gland, (the primary gland of the immune reactions) of irreplaceable immature immune cells. Each of these cells could have multiplied and developed into an army of valuable cells to combat infection and growth of abnormal cells. When these cells are used up permanent immunity may not appear. Work at the Arthur Research Foundation in Tucson, Arizona estimates that up to 60% of our immune system may be exhausted by multiple mass vaccinations. With naturally acquired immunity, only 10% of immune cells are lost.
This constitutes a grave concern for vaccinations ruining the immune system”―Patricia Jordan. “We know now that vaccine administration with adjuvant ruins the host’s viral defense program and at the same time mutate the genes, specifically the P53 oncogene that is responsible for tumor suppression, the adjuvant and the viral proteins together result in the annihilation of the very defense system the host was given to fight off both infection and cancer. Vaccines cause infection and vaccines cause cancer. Read all about it in the p53 tumor suppressor gene by Author David Ollie Published on Nov 4, 2004.”―Patricia Jordan. “In veterinary medicine we have long known the post vaccination sequele that results in seizures, epilepsy other demyelization diseases.
We have as a profession acted 'dumb' in recognizing the training difficulties, regression from socialization, increase in aggressiveness, development of phobias, attention deficit disorders, increased anxiety, irritability and a whole host of behavioral disorders that parallel what they have found in children and adult humans following vaccine administration. As a veterinary homeopath I have many, many cases where the vaccine has brought these events on distemper and rabies more frequently but any of the vaccines seem capable.”―Patricia Jordan. “Ever wonder why so many children suffer peanut allergies today?
What do you think happens when you inject peanut oil into the mammalian immune system and the body responds by turning on the peanut oil as if on terrorists? There is woeful reason why cutting edge doctors were advocating glutathione injections and lecithin supplementation for their patients. Cholesterol and phosphatidyl choline (lecithin) are used to make gobs to stick subunit particles on in the chase for another vaccine; did they make a 'better or safer' vaccine? Problem is that these components are part of the body's matrix, specifically part of nerves, and therefore we are at risk of attack by our own immune system thanks to the researchers developing these weapons of mass destruction, weapons that will turn our own immune systems against ourselves.”―Patricia Jordan. “Vaccinated animals are not only getting cancer at the injection site, they are getting cancer at every level of the immune system including lymphoma and leukemia. Canine retrovirus associated with lymphomas is identified.
Thanks to the work ofDr. Larry Glickman at Perdue and the Haywood Study we see that only vaccinated animals are developing auto antibodies, from Dr. Jean Dodd's work we see the connection to thyroid disease from vaccines, from aggression and seizures and lowered fertility and immunosuppression, we now see the T cell suppression that results after vaccination generating a rise in the cases of fungal, Demodex, coccidia, parasites and other diseases that rely on the cell mediated immunity to fend off the problems like Lyme's disease and other diseases with intracellular pathogens.”―Patricia Jordan.