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The March 1991 memo, obtained by The Times, said that 6-month-old children who received their shots on schedule would get a mercury dose up to 87 times higher than guidelines for the maximum daily consumption of mercury from fish.
"When viewed in this way, the mercury load appears rather large," said the memo from Dr. Maurice R. Hilleman, an internationally renowned vaccinologist. It was written to the president of Merck's vaccine division.
Originally posted by xelamental
HCG (human chorionic gonadotropin) is the hormone tested for when checking to see if a woman is pregnant. Administration of hCG to a woman causes her body to mimic the symptoms of pregnancy. So what would you expect to happen if you inject hCG into a woman as part of a vaccine containing substances causing an immune response and inflammation of the injection site?
Interesting - I see your point.
The combination causes the body to develop an immune reaction to its own hCG, resulting in impaired fertility. It works even better if you combine it with a toxoid such as diphtheria or tetanus.
I never knew this.
This is why the inclusion of squalene, (sometimes listed as MF-59 or ASO3,) in vaccines is such a serious matter. Squalene administered this way has been shown to cause Gulf War Syndrome.
Glycine is a naturally occurring chemical in the human body.
Injecting an adjuvanted vaccine containing a naturally occurring body chemical can cause a long-term immune reaction against that chemical.
It would be surprising if injection of glycine did not have a deleterious effect in some patients.
This is the first plausible mechanism I have heard.
But - surely, it would be simple to scientifically test to see if a vaccine caused immune responses like this. Have the tests been run? Any research you can point me to? Great post.
CAN VACCINE ADJUVANTS CAUSE ALLERGIES AND ANAPHYLAXIS?
Requests for information on the types of adjuvants used in human vaccines have not been answered to date. We did find that adjuvants are used to create allergic animals for scientific study and also that peanut oil has been used as an adjuvant. Peanut is by far the most common food to cause anaphylaxis in young children. Is peanut oil, or a similar protein or portion of a protein used in human vaccines as an adjuvant or "protein coat" in the Hib vaccine?? Aluminum has also been used as an adjuvant and is known to cause allergies according to the studies below. Could the adjuvants used in vaccines over the last 15 years be creating anaphylactic and allergic children?
. . . Murine model of atopic dermatitis associated with food hypersensitivity states,"Female C3H/HeJ mice were sensitized orally to cow's milk or peanut with a cholera toxin adjuvant and then subjected to low-grade allergen exposure.....An eczematous eruption developed in approximately one third of mice after low-grade exposure to milk or peanut proteins......This eczematous eruption resembles AD (atopic dermatitis) in human subjects and should provide a useful model for studying immunopathogenic mechanisms of food hypersensitivity in AD."
Mechanism of vaccine induced diabetes and autoimmunity
Recently several investigators working on vaccines to control fertility used the diphtheria and tetanus toxoids to break immunological tolerance to HCG, human chorionic gonadotropin, in humans when the hormone is associated with the vaccine.
Animal studies of this phenomenon show the induction of autoimmunity is not limited to the use of Freund's complete adjuvant since the administration of the swine flu vaccine in combination with an neural extract has lead to the development of autoimmune neuritis and the administration of the pertussis vaccine with thyroid extract has lead to the development of autoimmune thyroiditis in rodents.
Is Effective Immunity Necessarily Coupled with Autoimmuninity?
. . . . studies (in cancer treatment) have shown that, when CTLA-4 blockade is combined with xenogeneic DNA vaccines or granulocyte-macrophage colony-stimulating hormone–secreting irradiated whole-cell vaccines, increased rejection of established B16 tumors occurs and is associated with hypopigmentation. (turning white a la Michael Jackson)
Adjuvant/Rheumatoid Arthritis in Mice
Adjuvant arthritis is a disease in mice that's much like rheumatoid arthritis in humans. In mice, the disease is induced by injection of vaccine adjuvants. They're then studied for research on human rheumatoid arthritis because it appears to be virtually the same disorder.
Adjuvant/rheumatoid arthritis in mice is induced by injection with Complete Freund's Adjuvant, which contains a substance that is normally found throughout the human body—collagen. This particular adjuvant is not legal for use on humans in the United States. Of course, neither is squalene, as it's never been approved by the Food and Drug Administration (FDA), though it's used in several swine flu vaccines currently being administered.
What Drives Adjuvant Use in Vaccinations
Very few live virus vaccines are used today. The most significant reason is the potential of mutation into more virulent diseases. This is not a science fiction fantasy, but has happened recently in Africa. In an attempt to save money, Nigerian children have been given live polio vaccines. The result is a new, highly contagious, and virulent form of polio.
Therefore, killed and recombinant viruses are used, often not including whole viruses, but only proteins. As a result, these vaccinations are far less effective, often to the point of uselessness. In an attempt to increase the likelihood of the vaccination working, adjuvants are added. They can increase the body's immunological response. They can also increase the response to other materials injected with the vaccine, including the adjuvants themselves.
It's clear that any claims of safety based on an adjuvant's being a substance that's natural to the body is, at best, mistaken. It is precisely this that makes them dangerous.
Vaccine Court: Hepatitis B Shot Caused MS
. . . the Court noted in the ruling. “But if any of the vaccine antigens shares a homology with the recipient’s antigens, the host’s immune response will attack both the vaccine antigens and the host’s antigens, resulting in an autoimmune response. This concept is also known as molecular mimicry and is well-established in immunology.”
Hepatitis A vaccine associated with autoimmune hepatitis
The recrudescence of this case following vaccination with inactivated Hepatitis A virus adds to the evidence that Hepatitis A virus may trigger autoimmunity against the liver. It should not be interpreted as a side effect based on the vaccine’s track record of safety, but reveals potential connections between two apparently disparate liver pathologies.
Meningococcal molecular mimicry and the search for an ideal vaccine.
The carbohydrates expressed on the surface of meningococcal strains of groups B and C mimic those commonly found on human cells and thus are not functionally antigenic in infancy. In order to develop an effective vaccine, it will be necessary to find ways of circumventing this molecular mimicry.
Acquired autoimmunity after viral vaccination is caused by molecular mimicry and antigen complimentarity in the presence of an immunologic adjuvant and specific HLA patterns
Acquired autoimmunity syndromes occur after viral vaccinations. Molecular mimicry is involved in these phenomena as is the necessity for the presence of two chemically complimentary antigens and an immunologic adjuvant. The HLA pattern of the host is also an important factor.
The example used to explain these phenomena is demyelinating disease that follows hepatitis B vaccination. The somatic antigen of the hepatitis B virus in the vaccine has chemical complimentarity with the Epstein-Barr virus antigen in the vaccine recipient. The Epstein-Barr virus shows molecular mimicry with human myelin. The immunologic adjuvant is either present in the vaccine or muramyl peptides in the individual who is vaccinated.
Why more than one type of autoimmune disease occurs is explained by the fact that specific autoimmune T-cells have been shown to develop clones that attack multiple human tissues.
Immune System Sees Squalene as an Enemy to Attack
One of the great distinguishing characteristics of the immune system is something akin to a highly sensitive innate intelligence that has evolved over eons to be able to respond very precisely to what it deems to be a threat to the body. Because the body contains many types of oily molecules and lipids, it may be that when an oil is injected, the immune system responds to it not only specifically, but with heightened intensity because the oil adjuvant resembles so closely the natural oils found in the body. A “cross reaction” then happens, sending the immune system into chaos destroying any oils found anywhere in the body that resemble the adjuvant oil. Demyelinating diseases like multiple sclerosis are an example of this destructive autoimmune process.
. . . . . “When UCLA Medical School’s Michael Whitehouse and Frances Beck injected squalene combined with other materials into rats and guinea pigs back in the 1970’s, few oils were more effective at causing the animal versions of arthritis and multiple sclerosis”, writes Matsumoto. In 1999, Dr. Johnny Lorentzen, an immunologist at Sweden’s Karolinska Institute proved that on injection, “otherwise benign molecules like squalene can stimulate a self-destructive immune response”, even though they occur naturally in the body. Other research institutes have also shown that the immune system makes antibodies to squalene, but only after it is injected.
. . . . . This phenomenon is also known as ‘molecular mimicry’, where the immune system forms antibodies against one of its own structures and will continue to attack the ‘self’ molecule in the body that resembles the one in the germ, or as is the case with squalene, an identical substance that is naturally present in the body. Once this self-destructive process begins, it never stops as the body continues to make the molecule the immune system is now trained to attack.
. . . . . Matsumoto reports that Soviet bioweaponeers used the principal of molecular mimicry in the 1980’s to engineer a ‘designer disease’ that would attack myelin. By splicing a fragment of myelin basic protein into legionella bacterium, they created what amounted to a living “nano-bomb”, which they injected into guinea pigs. What they found was that the immune system quickly cleared the legionella bacterium, but the myelin molecule, smuggled in by this microbial “Trojan horse” initiated a second wave of disease which caused experimental allergic encephalomyelitis, the animal version of MS. The Soviets recognized this creation for what it was – a biological time bomb!
Contraceptive vaccine assessment based on a murine ZP3 mini-autoantigen
A summary is presented of published and some unpublished observations from studies on the immunological response of mice to a 13-mer peptide of the murine ovarian zona pellucida glycoprotein ZP3. The findings have the following implications for the design of immunocontraceptive vaccines. To be reversible, a ZP3 vaccine must not contain pathogenic T cell epitopes of ZP3, but contraception without autoimmune oophoritis may be feasible. The immune response to the ZP3 mini-autoantigen is highly variable among inbred mouse strains, suggesting that a single oophoritogenic peptide would not achieve irreversible contraception in an outbred population. The discovery of antigen mimicry at the level of T cell peptide has thrown doubt on the validity of current strategy in detecting relevant self-antigens that might cross react with vaccine immunogens and on the feasibility of fully predicting the cross-reactive autoimmunogenic potential of a peptide or polypeptide vaccine antigen. Autoantibodies directed against epitopes outside the ZP3 mini-autoantigen, produced by immunization with the pure T cell epitope, react with high affinity, with native zona pellucida, and may be useful in identifying B cell epitopes in ZP3.
Originally posted by k3456789
reply to post by paxnatus
mercury and squaline in vacciness are the problem so is the lying gov and cdc
Originally posted by OhZone
Originally posted by k3456789
reply to post by paxnatus
mercury and squaline in vacciness are the problem so is the lying gov and cdc
Before pronouncing that Mercury & Squaline are the problem, don't you think it would be wise to look at other connections; such as those I posted above, as well as those I posted on other pages here?
For some reason it seems that no one is interested in considering the role of DIET in these conditons. Ignoring it won't make it go away.
Autism, causes something called "leaky gut syndrome". This means the body lacks the enzymes to breakdown certain amino acids, I think there are 22 different aminos that fall into this category.
Instead of being broken down and absorbed by the digestive system that go straight into the blood stream, producing a toxic effect. One I have seen in action is the protein binding agent called caesin. Caesin is the end product of milk.
Once caesin enters the blood stream it becomes a morphine or opoid derivative. If an autistic child ingest a caesin product there are immediate erractic behavioral changes. Once the product is in the system "the crave begins" If the child does not get more, then you see withdrawal like behavior.
Originally posted by orwellianunenlightenment
. . . Our society has been increasingly viewing emotion as both feminine and valid, and logic as irrelevant (Don't anybody, including our very selves, dare point out the consequences of this game of choice we all play, and there are consequences. Such is irrefutable.). As such, many, particularly males, will develop autism, as they have not yet developed the will to not respond to these damaging, half-sided views masquerading as the end-all-be-all. They are cursed by the words of society. Sure, there are almost certainly chemical conditions which make autism more likely, but the environment in which they develop seals the deal. . . . .
Originally posted by Kailassa
Originally posted by orwellianunenlightenment
. . . Our society has been increasingly viewing emotion as both feminine and valid, and logic as irrelevant (Don't anybody, including our very selves, dare point out the consequences of this game of choice we all play, and there are consequences. Such is irrefutable.). As such, many, particularly males, will develop autism, as they have not yet developed the will to not respond to these damaging, half-sided views masquerading as the end-all-be-all. They are cursed by the words of society. Sure, there are almost certainly chemical conditions which make autism more likely, but the environment in which they develop seals the deal. . . . .
All you're doing is showing you understand nothing about autism.
It has nothing to do with not embracing "all three sides of the coin" ...
When my autistic child was first gently wrapped in a blanket he screamed in terror, and he screamed even harder when he was cuddled. Right from the start he refused to make eye-contact. He couldn't be carried out of the room he'd been born in without a panic attack for the first few months.
So was he "cursed by the words of society" while still in the womb, or is 5 minutes in this world's atmosphere enough to do it?
And how do you explain the fact that the more exposure he's had to this world the more "normal" he's become? Shouldn't he be becoming more and more autistic as the terrible pressures of modern society exert their inevitable consequences?
Beware of too much philosophising based on too little fact.
It's inclined to leave a fellow with a swollen cranium and a sticky keyboard.