“…only 1 in 10,000 HPV-infected women develop cervical cancer.” --https://healthimpactnews.com/2015/study-hpv-infections-not-necessary-for-development-of-cervical-cancer-are-hpv-vaccines-worthless/

 

“I predict that Gardasil will become the greatest medical scandal of all times because at some point in time, the evidence will add up to prove that this vaccine…has absolutely no effect on cervical cancer and that all the very many adverse effects which destroy lives and even kill, serve no other purpose than to generate profit for the manufacturers.” -- Dr. Bernard Dalbergue, a former pharmaceutical industry physician with Gardasil manufacturer Merck

 

“No vaccine manufacturer shall be liable…for damages arising from a vaccine-related injury or death.”– President Ronald Reagan, as he signed The National Childhood Vaccine Injury Act (NCVIA) of 1986,absolving drug companies from all medico-legal liability when vaccines kill or disable children

 

“The 271 vaccines in development span a wide array of diseases, and employ exciting new scientific strategies and technologies. These potential vaccines – all in human clinical trials or under review by the Food and Drug Administration (FDA) – include 137 for infectious diseases, 99 for cancer, 15 for allergies and 10 for neurological disorders.” --“Statement from the Pharmaceutical Research and Manufacturers of America (PhRMA) - the pharmaceutical industry’s trade association and lobbying group.(http://phrma.org/press-release-medicines-in-development-vaccines#sthash.rI4cQ6Tg.dpuf)

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The #1 talking point of Big Pharma, Big Vaccine, the CDC, the AMA and the American Academy of Pediatrics when they try to justify the use of the neurotoxin aluminum (and the neurotoxin mercury) in their vaccines is this one: “humans shouldn’t be afraid of the small amount of either aluminum or mercury that is or has been in many human and animal vaccines.”

 

They say, truthfully, that aluminum is the third most common element in the earth’s crust, behind oxygen and silicone.  Oxygen makes up about 47% of the earth's mass. Silicon is second at 28%, followed by aluminum at 8%. They also say that aluminum may be just as harmless as oxygen and silicone and that humans are also exposed to aluminum in oral antacids and underarm anti-perspirants and that those products haven’t yet been “conclusively” proven to have caused “statistically-significant” health problems. They fail, of course, to mention that the “studies” that prove aluminum’s safety (and efficacy) were designed, performed and paid-for by the very industries that benefit from the unregulated, unexamined and widespread use of injectable aluminum in America’s over-vaccination schedules.

 

It is important to note that the reason that aluminum has been used in vaccines for the last 80+ years is because it has been found to be an “adjuvant” (defined as “a substance that enhances the body's immune response to an antigen.” An “antigen” is “a toxin or other foreign substance that induces an immune response in the body”. Interestingly, nobody really understands exactly how aluminum performs as an adjuvant, and there is a desperate search for other adjuvants because the vaccine industry understands just how toxic it is.

 

Adjuvants, when incubated with certain viral particles in the lab, usually enables the stimulation of antibodies and thus usually produce temporary, artificial, serological immunity against the intended virus, viral particle, bacterial particle or toxoid molecule.

 

This plausible vaccinology theory ignores the fact that intramuscularly-injected aluminum can also very easily cause an over-stimulation of antibodies to some of the normal body tissues of the vaccinee, which is known as a “vaccine-induced autoimmune disorder”. How that can happen is dealt with later in this article.

 

<<<The Differences Between Oral and Injectable Aluminum>>>

 

It is important to understand that there are important differences between orally-ingested aluminum (in some antacids) and intramuscularly-injected aluminum (which is commonly used in many vaccines).

 

Orally-ingested aluminum isoorly absorbed through the intestinal mucosa into the blood stream. Only a tiny fraction of the total dose (0.3%) is absorbed, meaning that 99.7% of the ingested aluminum is NOT absorbed and thus passes out of the body through the stool.

 

There are questions as to how toxic swallowed aluminum is to the bowel mucosa or intestinal bacteria or how damaging to the body’s cells is the 0.3% that gets into the bloodstream. It depends on the total body burden of other poisonous metals like lead, mercury, iron, cadmium and manganese and the presence of other toxins like fluoride, psychiatric drugs, vaccines, food additives, etc.).

 

Another important factor is the health and maturity of the blood-brain barrier (or the placental barrier in the case of women who are unfortunate enough to have been given vaccinations during their pregnancies, thus exposing their fetuses to potentially brain-damaging substances). The blood-brain barrier is discussed a bit further on.

 

Most of the aluminum that actually gets into the blood stream is eventually excreted through the kidneys, although some of it can be absorbed by any organ in the body. 

 

However, aluminum (as is Eli Lilly’s vaccine preservative thimerosal [which is 50% mercury] is known to be highly toxic to every organ system and its mitochondria, especially kidneys, thyroid, liver, bone and brain.  Thimerosal, it must be acknowledged, was once widely used in infant vaccines, until the American Academy of Pediatrics pleaded to the vaccine manufacturers to take it out of the baby shots because of the high probability of its being the cause of the sudden and dramatic rise in the incidence of autism over the past generation.

 

(Recall that any toxin that gets into the bloodstream can potentially adversely affect every other organ in the body.) The degree of damage inflicted depends partly on the nutritional health of the individual, the amount of anti-oxidants in the diet, the detoxifying systems in the liver – and, as mentioned above, the blood-brain barrier.

 

<<<The Blood-Brain Barrier>>>

 

The normal brain is fortunately relatively safe from many of the blood-borne toxins that animals can be exposed to - because of the blood-brain barrier (BBB). The BBB is a system of unique brain capillaries, whose endothelial cells have unusually “tight junctions” between each cell. Those endothelial cells are supposed to keep large molecules and infectious agents out of the cerebrospinal fluid (CSF), the fluid that bathes the brain and spinal cord and therefore away from the very vulnerable central nervous system (CNS).

 

The BBB is a very effective defender of the brain, unless it is immature (is as the case for all small infants) or unless it is aged or diseased (which is the norm for the elderly, the acute or chronically ill, the highly medicated, the highly vaccinated and for those who are exposed to toxic substances that are known to harm the BBB). Toxins known to harm the BBB include solvents, herbicides, pesticides, viruses, bacteria, street drugs, many pharmaceutical drugs, toxic foods, toxic water, toxic metals (including the aluminum and mercury in vaccines), electromagnetic radiation, etc.

 

As is touched on above, the aluminum in vaccines is designed to hyper-stimulate antibody production against various infectious antigens. The vaccine antigens that will be marketed to the public are first manufactured or grown in chicken or duck eggs, chicken kidney cells, mouse brain cells, African green monkey kidney cells or human fetal cells in the laboratories of Big Pharma’s vaccine manufacturers like Merck, GlaxoSmithKline (GSK), Sanofi-Pasteur and MedImmune.  Then aluminum nanoparticles are adsorbed onto those antigens in vats. Then a variety of other substances are added, including preservatives (such as mercury, antibiotics, formaldehyde, phenol, phenoxyethanol), then placed into multiple-dose vials and sent to clinics.

 

When the aluminum-containing inoculum is eventually injected into the muscle tissue of patients, the body’s immune system is supposed to produce antibodies (immunoglobulins) against the antigen onto which the aluminum nanoparticles were adsorbed. The intensity of antibody production varies tremendously, from zero effect to hyperimmune responses.

 

Whether the injection accidentally went into the subcutaneous fat, directly into a blood vessel or into scar tissue would account for some of the variance in effectiveness and duration of the antibody response.

 

What is for certain is that any antibody response is only temporary. Some of the adverse effects, like the high incidence of fainting and the POTS syndrome (especially following the Gardisil vaccinations), might be because the vaccine was injected into a small blood vessel and thus directly into the bloodstream instead of the muscle.

 

What is also a certainty is that vaccinations have zero (or even negative) effects on cellular immunity, the equally important second half of the body’s immune system. The two halves of that system – the cellular and the serologic – are both involved in natural childhood infections, and that reality accounts for the fact that natural infections result in life-time immunity (whereas vaccinations require periodic boosters, which do nothing for enhancing cellular immunity).

 

But serious unintended consequences from vaccines can occur, for the injected material will – to the vaccinee’s mononuclear cells (macrophages) - be regarded as a foreign body. The  main purpose of macrophage’s is to swallow and neutralize foreign bodies that penetrate the body’s protective skin or mucosal surfaces, thus ameliorating the toxic effects of germs, slivers, cat bite saliva, injected vaccine ingredients, etc.

 

<<<How Can Aluminum-Adjuvanted Vaccines Cause Neurotoxic Disorders Like Autism or Dementia?>>>

 

I describe below two of the serious un-anticipated and unwanted outcomes that can happen when aluminum-coated antigens are injected into an animal’s muscle tissue:

 

1) After the body’s macrophages ingest the aluminum-coated vaccine material, they will migrate into the lymphatic system (including regional lymph nodes), and then they will go into the bloodstream, which eventually goes to many other distant organs, including the liver, spleen, bone, brain.

 

Macrophages are capable of slithering through the “tight junctions” that are located between the BBB’s endothelial cells. When the BBB is healthy it will keep out toxic substances such as large proteins, viruses, bacteria, large molecule drugs, toxic metals and other toxic substances such as dissolved aluminum ions.

 

However, if the BBB is immature or diseased, some of those toxic substances are at risk of getting into the cerebrospinal fluid. So, whereas dissolved aluminum in the blood usually can’t get into the brain by itself, when it is inside a macrophage it can enter into the protected space of the brain and thus potentially poison brain cells (neurons, nutrient glial cells and synaptic cleft organelles where neurotransmitters do their magic). Macrophages appear to be identical to brain microglia in that they have similar nutrient and de-toxifying functions.

 

The above phenomena have been well studied and are the mechanisms that explain how injected aluminum-adjuvanted material can cross the diseased or aged BBB of so-called pre-dementia patients or cross the immature BBB into the brains of infants and thus condemn some of those victims to come down with a vaccine-induced dementia or a vaccine-induced autistic spectrum disorder, ADHD, or other behavioral or neuro-developmental disorder.

 

And, of course, a vaccine-damaged BBB will increase the risks of lead-induced brain damage to children (as in Flint, Michigan), which is why lead-poisoned infants and children should probably not be vaccinated until their blood lead levels are at zero.

 

<<<How Can Aluminum Adjuvants Cause Autoimmune Disorders?>>>

 

2) The second serious thing that can happen when aluminum is injected into animal tissue – particularly the small bodies of children or infants - is that the needle can be expected to traumatize whatever tissues it pierces.

 

That trauma, plus the inevitable inflammation that develops from the vaccine ingredients, will cause the break-down of other para-muscular tissues, such as, obviously, the now-damaged muscle tissue, area blood vessels, white blood cells, platelets, blood clotting factors, collagen tissue, nerve tissue, fat, myelin, etc, likely coating some of these otherwise normal cells with the aluminum adjuvant and setting up the possibility for the body’s immune system to develop antibodies against its own tissues, which is the definition of an autoimmune disorder.

 

So patients with autoimmune disorders like Macrophagic Myofasciitis (MMF), Autoimmune/inflammatory Syndrome Induced by Adjuvants (ASIA, aka Shoenfeld’s Syndrome), lupus, juvenile rheumatoid arthritis, dermatomyositis, scleroderma, idiopathic thrombocytopenic purpura, Guillain-Barre syndrome, multiple sclerosis, Gulf War Syndrome, Type 1 or Type 2 diabetes, Hashimoto’s thyroiditis, etc may actually have vaccine-induced autoimmune disorders. (Google research scholars such as Romain Kroum Gherardi, Yehuda Shoenfeld, Chris Shaw, Lucija Tomljenovic, etc for more.)

 

There are a multitude of case reports and case series in the world’s medical literature of vaccine-induced autoimmunity. They only seem to get published in the journals that aren’t subsidized and don’t accept advertising money from pharmaceutical companies (and don’t have editors who have been co-opted by Big Pharma, the CDC or the AAP).

 

These vaccine-induced autoimmune disorders are iatrogenic disorders (doctor-caused, prescription drug-caused, vaccine-caused, surgery-caused) and thus their existence makes them taboo subjects - not to be discussed publically. But in the honorable “first do no harm” profession that I proudly joined after medical school 40+ years ago, drug-induced, iatrogenic disorders were always to be at the top of the differential diagnosis list. That teaching appears to have disappeared in today’s Big Business model of medicine.

 

But, for the sake of our vulnerable patients, especially our babies and the elderly, who are getting sicker and more chronically ill as more and more drugs and vaccines are prescribed and ingested, honorable physicians and paraprofessionals should be actively considering the possibility of iatrogenesis whenever they are faced with chronically ill or autoimmune disordered patients.

 

<<<Further Vaccinations to Patients who Have Vaccine-Induced Autoimmunity or Vaccine-Induced Neurodevelopmental Disorders Should be Contraindicated>>>

 

Vaccine-induced injuries, deaths and autoimmune disorders are increasingly common among fully vaccinated populations. Some say that the increasing incidence of chronic illnesses in fully-vaccinated children is reaching epidemic proportions. The correlation between the huge increases in dementia among America’s fully-vaccinated older adults (who get yearly mercury injections in their flu shots and then get yearly aluminum-containing pneumovax shots) needs to be thoroughly noted.

 

The worsening of toxic disorders caused by heavy metal exposure is known to happen with every additional exposure to the toxin. Two toxins together can cause enormous synergistic (as opposed to additive) increases in toxicity. That phenomenon of synergy appears to apply when aluminum and mercury vaccines are co-administered. Thus, if vaccine-induced disorders are not recognized, the already poisoned patients will have their autism, autoimmune disorders, chronic illnesses or  dementia worsen, and larger long-term health care costs and more human suffering will occur – exactly the opposite of what is the intent of the physician pledge to “first do no harm”.

 

There are a number of whistle-blower experts (see below) who are trying to alert others in positions of authority (including doctors, journalists and law-makers) to the dangers of Big Pharma’s highly-profitable over-vaccination business plan. These out-numbered and silenced whistle-blowers are stepping on some very big toes, including huge multinational pharmaceutical corporations that have large numbers of clever lawyers, cunning front groups, well-paid lobbyists and control of what gets reported on the mainstream news. That combination can easily destroy the careers of honest altruistic researchers that threaten Big Pharma’s financial bottom line – and they have – most dramatically and cruelly in the case of Dr Andrew Wakefield (watch one of his powerful talks on YouTube before reflexively repeating the Big Media-propagated Big Lie: “Wakefield’s Lancet article proving the connection between Glaxo’s MMR vaccine and serious measles virus intestinal infections in severely-involved autistic kids was discredited years ago”).

 

What makes the problem urgent is that the medical establishment is allowing itself to be repeatedly brain-washed by Big Pharma’s criminal smearing of honest whistle-blowing physician-scholars like Wakefield, Suzanne Humphries, Sherri Tenpenny, Russell Blaylock, Diane Harper, Toni Bark and Kelly Brogan – as well as non-physician experts like Stephanie Seneff, Brian Hooker, Barbara Loe-Fischer, Gary Goldman, and Robert Kennedy, Jr. (google each of them before dismissing this column  and then listen to their testimony which is all over YouTube. One can find links to everything at one website: http://www.vaccinesrevealed.com/.

 

If the medical establishment remains in denial or ignorance about the dangers of vaccines, the financial impact of just the three vaccine-induced disorders mentioned above will not only dramatically increase in incidence and intensity but the escalating multi-billion dollar cost of care for these permanently disabled autistics, “Alzheimer’s Disease” patients and the “mysterious” chronically-ill autoimmune disordered patients will surely bankrupt the nation (if the Pentagon doesn’t do it first).

Original posted here Posted at: https://www.transcend.org/tms/2017/03/aluminum-autoimmunity-autism-and-alzheimers/