High Levels Of Aluminium Found In Autistic Brains

Prof. Christopher Exeley, Professor in Bioinorganic Chemistry at Keele University, has discovered that in the autistic people he studied of around 13, 14, and 15 years of age that “there (was) more aluminium than seen in any other circumstance” (detected in their bodies).

Professor Exeley states that his research career (1984-present) has focused upon an intriguing paradox; “How come the third most abundant element of the Earth’s crust (aluminium) is non-essential and largely inimical to life?”

“I am also fascinated by the element silicon in relation to living things which, as the second most abundant element of the Earth’s crust, is also almost devoid of biological function.

One possible function of silicon is to keep aluminium out of biology (biota) and this forms a large part of the research in our group. We are also interested in biological silicification.”

Toxic aluminium found in alarmingly high amounts in the autistic brain.

“This is the first time in any human brain tissue we have seen this, this is a standout and unique observation in autism. For myself, it very much implicates aluminium in the ethology of autism. That doesn’t mean aluminium causes it, but it means it’s almost certainly playing a role in the disease.”

“When we looked at people’s brains with a diagnosis of autism, we found something that we have never seen yet in any other set of human brains. We found that the majority of aluminium was actually inside cells; intra-cellular. Some of it was inside neurons, but actually the majority of it was inside non-neuronal cell populations.”

“So we found that these cells were heavily loaded with aluminium. We also found evidence that cells in the lymph and in the blood were passing into the brain. So they were carrying with them a cargo of aluminium from the body into the brain.”

Most shockingly, this urgently needed study was not funded by any government, but by non-governmental philanthropy.

Autism, which is one of the major illnesses of our time, is not being actively studied in mainstream science.

Exeley stated in the interview that “no government funded this research, it came because of philanthropy, it came because of individuals who wanted to know answers and were prepared to use their own money.”

“We pay our government, and our government should really be using our money to fund this type of research.”

They key difference to highlight is that when we ingest aluminium orally, it is subjected to our digestive tracts; and gets excreted rather than absorbed — as aluminium has no role in the human body.

When it is injected, aluminium bypasses our bodies’ natural defenses, and lodges itself in tissues throughout the body, most notably the brain; which is a highly absorbent, 60% fat organ that sees high bloodflow compared to other areas of the body.

This means lots of resources are being transferred through the brain all the time, a blood-brain barrier is a natural way of keeping out unwanted substances and absorbing useful resources like oxygen, it is highly likely that an intravenous injection of toxic substances like aluminium may breach the blood-brain barrier and implicate toxicity.

This distinction is of toxicological significance — and implicates aluminium adjuvants in intravenously applied vaccines as something of serious concern.

Getting aluminium out of the body.

Silica has been found to reduce aluminum levels drastically in the body. It does this by binding with its molecules and extracting them out of brain cells and ultimately out of the body through urine and other means.

Ground-breaking research done by Dr. Exeley found that water high in silicic acid (oxygenated silica) had a positive effect on autistic children. Exeley has found that aluminum levels were lower in the children by 50 to 70 percent who drank this kind of water.

He then did the same study with Alzheimer’s Disease (AD) patients. After 13 weeks of drinking high-silica water, the same results were achieved. In the AD patients, eight out of fifteen no longer showed neurological deterioration and three showed “substantial cognitive increase.”

Dr. Exeley used Spritzer (a Malaysian bottled water) for the study, but other waters that contain high amounts of silica include Volvic and Fiji (Fiji comes in a BPA-free bottle). His suggested protocol for helping to remove aluminum from the brain is to consume 1.5 liters of high-silicic water for at least 5 days. He suggests drinking the entire 1.5 liters within an hour for the best results. Higher aluminum toxicity levels may require higher amount of water.

Diatomaceous earth (DE) is another great source of silica since it is made up mostly of the substance. Diatomaceous earth is actually millions of tiny, fossilized aquatic microorganism called “diatoms” that are ground up into a fine, white powder. Besides aluminum detoxification, DE also chelates other heavy metals, helps with GI health, and can give you more energy.

In addition to high-silicic acid waters and DE, cucumbers, bananas, bentonite clay, and horsetail herb also contain high amounts of silica.

Add at least one of the following nutritional substances to your diet every day. All of these not only have the ability to detox the body from heavy metals, but are also neuroprotectants and immune system boosters:

  • Cold pressed unrefined organic coconut oil
  • Chia and flaxseed
  • Milk thistle
  • Vitamin C (and foods rich in this vitamin)
  • Spirulina and chlorella
  • Foods such as garlic, cilantro, and parsley that can help eliminate heavy metals such as aluminum and mercury from your body
  • Fresh, filtered water (and plenty of it!)
  • Carbon 60, may chelate metals in the safest way currently known.
  • The Andy Cutler Protocol, which is also a safer way of chelating metals from the brain and body.

Autism Epidemic: The Hyper-Masculinization Theory

Autism Spectrum Disorder (ASD) is more prevalent now than ever before, it’s a topic rarely discussed — in previous articles I have put forward several theories as to the cause of the illness; including but not limited to exposure to toxins in pharmaceutical vaccines, the genetic and gender roles in the origins of the illness, environmental traumas, prenatal exposure to hostile chemical agents, and so on.

Autism has skyrocketed. The mainstream media and the medical establishment have attributed this to ‘greater rates of diagnosis’ and a more comprehensive understanding of autism as a condition – I disagree with this poor explanation; autism is very noticeable and identifiable.

As a disclaimer, and to distinguish — autism has numerous manifest forms; generally recognized in problems with social communication and social interaction, and/or restricted, repetitive patterns of behavior, interests or activities — there are numerous hues of the “autistic” profile, as per the varying extent of the condition’s causative effects.

Endocrine disruptors are likely having a major role in the onset of autistic spectrum’s symptoms in people. Endocrine disruptors are chemicals that may mimic and interfere with the body’s chemical messenger system (endocrine system) and produce adverse developmental, reproductive, neurological, and immune effects in both humans and wildlife — hormones, besides DNA, are directly responsible for what we are, physically, mentally, and emotionally.

Our hormones can make us more masculine or more feminine, decide where our bodies should build muscle, fat, affect our gynecology, alter the structure and thought processes of our brains; dictate our personalities, our behavior, our very perception of the world around us — the list is endless, this is crucial in understanding autism as an illness and how it manifests.

There is a growing recognition that even small amounts of endocrine-disrupting chemicals can have a deleterious affect on the development of the fetus, infants and young children.

All in all, most of these “autistic” profiles, any way you look at them, are extremely damaging to the fabric of our society (no, autism is not healthy or natural) and can be pinned to a few common likely causes.

On pharmaceutical vaccines, chronic immune system dysregulation:

A common argument against people who are skeptical of or criticize vaccines is that vaccines are the “magic bullet” to our health and wellbeing, that without vaccines we’d all die in some horrendous plague. This is patently false. Vaccines, like anything we put into our bodies, should be questioned and scrutinized.

Epidemiological studies (statistical surveys) show poorer long-term health is more common among the vaccinated who survive without serious injury than children who are not vaccinated — this condition is termed “vaccinosis”. (1234).

Gian Paolo Vanoli, a scientist, journalist and opponent of vaccinations, says that vaccines make people gay. This is one just account of the detrimental hormonal influences of vaccines.

Vaccines only engage part of the immune system, they intravenously introduce pathogens; a way the body cannot manufacture a proper adaptive response, the result is autoimmune disorders. In cases of immune system over activity, the body attacks and damages its own tissues (autoimmune diseases). Heightened body inflammation over a vaccinosis sufferers’ life results in numerous illnesses.

When people are subject to repeated vaccines, they predictably simulate a situation of suppressed cell-mediated immunity and heightened antibody responses. Why? Because that’s the goal of vaccination. If you make a list of the diseases that are characterized by suppressed cell-mediated immunity and heightened humoral immunity, you’re talking health conditions like asthma, allergies, eczema and autoimmune diseases including Crohn’s, Vitiligo, Multiple Sclerosis, Sjogren’s syndrome, Hashimoto’s, etcetera.

We cannot and will not eradicate all disease with vaccines. We have merely traded acute illnesses from which most recover for chronic illnesses for which modern medicine has no cure.

It’s become increasingly apparent that vaccines turn the guns of immune defense inwards.
  • In a 1997 study in New Zealand, 1265 children were surveyed: twenty-three percent of the vaccinated children experienced asthma and thirty percent suffered from allergies. The unvaccinated children did not have a single incident of these illnesses.
  • In a 2004 British Study of 30,000 children, vaccinated children had a 5.04 increased risk of asthma, while the unvaccinated only had a .36 percent prevalence.
  • In a 2011 German Study of 8000 children, vaccinated children had at least two to five times more diseases and disorders than unvaccinated children.

In patients with an autoimmune disorder, the immune system can’t tell the difference between healthy body tissue and antigens that need to be attacked. The result is an immune response that destroys normal body tissues. This response is a hypersensitivity reaction similar to the response in allergic conditions. Vaccinations have been shown to induce autoimmune disorders.

Interestingly, there’s a study out of Kobe University in Japan where they took mice and put them on a rigorous vaccination program. They wanted to see if they could develop excessive antibodies as seen in autoimmune disease. And they found that at a certain threshold they could consistently and reliably induce autoimmune disease by simply giving enough vaccinations. (source)

This vaccine-induced autoimmune disease may explain the onset of autism in some people who are genetically susceptible or otherwise. Is autism an autoimmune disorder? Most likely.

The Kobe University study authors concluded:

“Systemic autoimmunity appears to be the inevitable consequenceof over-stimulating the host’s immune ‘system’ by repeated immunization with antigen to the levels that surpass the system’s self-organize criticality.”

In other words, they found that, not only is vaccination a possible or even probable cause of autoimmune disorders, but that chronic diseases are the inevitable result of vaccinations!

This study was done with mice. This begs the question, ‘Has this been replicated in humans?’ Unequivocally yes. This experiment has been done and it’s called the last 70 years.

Autoimmune diseases have increased in quantity and variety as the number of vaccinations has increased over the last 70 years. There are over 100 autoimmune diseases. Studies with monogenetic twins have revealed that genetic influences only account for 25–40% of the disease risk making environmental influences the predominant factors. (7) Regardless of genetic vulnerability, one’s environment determines whether genes for autoimmunity are expressed.

There is a reason the fastest growing subset of diseases in the US and the world are autoimmune diseases. This is because we’re producing them. It’s a growth industry. As vaccines have increased in number, so have the number of cases of autoimmune disease.

Currently, there are 38 vaccines on the recommended schedule, with even more in some US states. There are many more vaccines in development. I predict a worsening epidemic of allergies, asthma, autoimmune and other diseases caused by an atrophy of the cell-mediated immune response as more vaccines are added to the vaccine schedule. We are only seeing the tip of the iceberg with vaccine-induced disease.

In vulnerable children, vaccines cause autism, seizures, mental retardation and so many other health issues. One must also take into account the fact that for every severe reaction, vaccine provoke less acute effects like confusion, language difficulties, memory issues, irritability, mood alterations, combativeness, difficulty concentrating and behavioral problems. (source). This sounds very much like ADD and ADHD, which are sweeping the child population in epidemic proportions.

Read more at MyersDetox.

Sources for information on vaccines:

  1. Drtenpenny.com
  2. Vaccineresearchlibrary.com
  3. Novaccine.com
  4. 909shot.com
  5. Thinktwice.com
  6. Nvic.org (National Vaccine Information Center)
  7. Vaccinetruth.org
  8. Vran.org (excellent Canadian site)
  9. Childhoodshots.com

The Hyper-Masculinization Theory

The 2004 book by Simon Baron-Cohen called “Prenatal Testosterone in Mind: Amniotic Fluid Studies” and his 2003 book “The Essential Difference: Men, Women and the Extreme Male Brain”, dives into the role gestational endocrinology might have in influencing human minds, personalities and behavioral profiles.

One emerging theory suggests that autism may have something to do with high exposure to adverse hormonal influences in the womb — in effect interfering with the child’s otherwise stable development — and pushing their cognitive profile to become overly systemic, or at least inhibiting the formation of a healthy cognitive profile — the result seems to be an augmentation of the structured and logical male brain. A personality style guided overly by systems and order.

Slightly elevated levels of testosterone in fetuses have been linked to health defects and autism, and that autism-type disorders are four to nine times more common in boys.

Research indicates that mercury and aluminum components of vaccines may have synergistic toxicity with testosterone, which causes the autistic symptoms to emerge. It’s not surprising when you consider the rise of autism came in the 1930s when ethyl mercury was first commercialized in agricultural products and in vaccines.

To address people who claim that mercury isn’t in vaccines anymore; it’s simply not true that they’ve removed the mercury exposure from infant and fetal vaccines. Mercury has come out of some vaccines. It’s still in others, and they’ve targeted pregnant women with flu shots, and ethyl mercury in pregnancy is even more toxic in pregnancy than it is in infancy. Also, injected substances are more toxic than conventionally ingested substances. Mercury you consume orally is less of a danger than injected mercury.

Like it or not, vaccines are likely the largest source of one-time exposure to endocrine-disrupting chemicals in early infant development that may be responsible for these marginal fetal hormone-altering effects.

Natal and post-natal vaccinations are the only common logical stages wherein hormonal interference can take hold in a big way and change the biological course of someone’s life permanently.

Preterm delivery 4.7 times higher
Clear-cell adenocarcinoma 40 times higher
Neonatal death 8 times higher
Loss in second trimester pregnancy 3.8 times higher
Ectopic pregnancy 3.7 times higher
Stillbirth 2.4 times higher
Infertility 2.4 times higher
Early menopause 2.4 times higher
Breast cancer 1.8 times higher

For example, considering autism has been linked to testosterone, with boys having the condition far more than girls (at 80% of ASD cases being males), one study has shown that people with autism have more masculine facial structures than the average neurotypical person, pointing towards higher testosterone as a link.

A paper published in 2015 also found adults (both men and women) with higher prenatal testosterone had more masculine facial features, and that this is the group most likely to have the neurological profile known as autism.

The testosterone connection deepens, the lack of emotional intelligence in autistic people could be linked to the hyper-masculinisation associated with testosterone’s empathy-reducing effects on the brain — healthy men should have less empathy than women but should still have an emotional side; testosterone makes us more individualistic and antagonistic, hyper-masculinisation could push this to extremes. This capacity to empathize conventionally typically seems to be less prevalent in autistic people.

The hyper-specific interests of many autistic people perhaps alludes to the wiring of the archetypal male brain; the ability to focus on an objective and be undeterred by other interfering thought processes.

The effect on the autistic person’s emotional quotient seems to vary between overly sensitive and emotionally unpredictable, to overly systemic and rigid, or a combination of both, or a slight effect of any of these symptoms in the partial autistic condition known as Asperger syndrome. Interestingly, it seems to more commonly go the way of this hyper-systematized personality, though.

Returning to the testosterone link, the UWA research associate Syed Zulqarnain Gilani and his team developed a technique where 3-D photogrammetry — the science of making measurements from photographs — could score a face to be male or female, based on 11 facial features.

“First, we looked for features that distinguished between male and female,” Zulqarnain says.

“We found the autistic boys and girls had significantly more masculine gender scores than the non-autistic subjects.”

The study also found the more masculine the face, the more social communication difficulties the children in the ASD group had.

Pesticides could play a role in the autism epidemic.

Another study showed how elevated levels of a metabolite of the insecticide DDT in the blood of pregnant women are linked to increased risk for autism in the offspring.

The investigators found the odds of autism with intellectual disability in offspring were increased by greater than twofold for the mother’s DDE levels in the top quartile.


Dr. Stephanie Seneff, when asked “is there a toxic substance that is currently in our environment on the rise in step with increasing rates of autism that could explain this?” Seneff responded; “The answer is yes, I’m quite sure that I’m right, and the answer is glyphosate.” — This glyphosate is the active ingredient in RoundUp, a product made by Monsanto, which ranks as the number one herbicide used worldwide.

Russia looks to become top producer and exporter of organic food with President Vladimir Putin recently signing a new law regulating production, storing and transportation of organic produce in Russia. The decree bans agrochemicals, pesticides, antibiotics growth stimulators and hormones. Many countries have banned or are taking steps to ban glyphosate use, and move to cleaner foods.

Pregnancy is a delicate process that cannot be interrupted.

During pregnancy the hormonal levels of the mother are in flux, it’s a phase in which her body is carefully assembling new life in the womb.

Natal vaccines, such as the flu jab, cause a shock to the system that changes the hormonal profile of the pregnant mother, the developing child takes the biggest hit.

Did I mention that a stunning finding revealed that autism is highest in areas with the highest vaccination rates? Correlation or causation?

Vaccines and pesticides also have a endocrine-disrupting effect on the gestating mother’s child, the evidence supports this:

For example, in 2004, Alan Cantwell, M.D. raised concerns that 74 million children in Africa were discovered to be contaminated with a variety of female sex hormones, and that the injection of these was linked to an increase of sterility. Estradiol (E2), also spelled oestradiol, is an estrogen steroid hormone and the major female sex hormone, what is it doing in vaccines? — without a doubt I would link this to the rise in autism, homosexuality and gender-queerness.

The formative development of a person, involving the early biological emergence of a person’s distinct gender is an especially susceptible phase to disruption.

Aluminium and mercury, toxic adjuvants present in some vaccines are well-known potent endocrine disruptors. It’s no wonder many autistic kids show the signs of hormonal abnormality in their facial structure, as already mentioned – and that’s just the one’s that show an outward sign, it’s likely most have these irregularities but they may not be as outwardly noticeable.

Tyrone Hayes, University of CA professor was asked to study a chemical called atrazine, a widely-used herbicide manufactured by Syngenta. He found unexpected results: that it causes sexual abnormality in frogs and that it could potentially cause the same effects in humans (frogs changing from male to female). Herbicides like atrazine are detectable on and in most food — including food eaten by pregnant mothers and transferred to unborn babies.

Vaccines with heavy metals and viruses that cause inflammation, pesticides and any other similarly unnoticeable agents — the hormonal profile of the gestating mother will be forced to change to deal with the hostility, it looks like this may be at the expense of the fetus’ health — in nature, the mother’s body takes precedence over the unborn child, the mother’s body is the crucial supply line. For example, Dr. Deepak Chopra has claimed that hundreds of studies have confirmed that chemicals released by the pregnant mother’s body are transported into the womb and affect the unborn baby.

The start of the autism epidemic correlates closely with the phased introduction of the Hib vaccine plus the HepB vaccine in the late 1980’s/early 1990’s. At that time, both the Hib and the HepB contained high amounts of mercury and aluminum which significantly increased the exposure to infants to both of these toxic chemicals at a far earlier age than ever before (HepB: at birth and then 1-2, 4, and 6 months; Hib: 2, 4, and 6 months).

Although mercury has been reduced or removed in some vaccines since 2003, mercury is still a component in most flu vaccines. The number of infant vaccines with aluminum-based adjuvants administered by 18 months of age has increased by 54% since 2000, and the amount of aluminum administered has increased by 23%.

In an article for Mothering Magazine, Dr. Bob Sears warned about the aluminum content found in infant vaccines:

In other words, a newborn who gets a Hepatitis B injection on day one of life would receive 250 mcg of aluminum. This would be repeated at one month with the next Hep B shot. When, at two months, a baby gets its first big round of shots, the total dose of aluminum could vary from 295 mcg (if a non-aluminum HIB and the lowest-aluminum brand of DTaP are used) to a whopping 1225 mcg (if the Hep B vaccine is given along with the brands with the highest aluminum contents). These doses are repeated at four and six months. With most subsequent rounds of shots, a child would continue to get some aluminum throughout the first two years. But the FDA recommends that premature babies, and anyone with impaired kidney function, receive no more than 10 to 25 mcg of injected aluminum at any one time.

So there’s how it is; aluminum and mercury are both endocrine disruptors, as well as neurotoxins, and both can be particularly toxic when exposed to testosterone — is someone targeting men by needlessly putting these substances in vaccines? Of course.

There is no end to the tricks that endocrine disruptors can play on our bodies: increasing production of certain hormones; decreasing production of others; imitating hormones; turning one hormone into another; interfering with hormone signaling; telling cells to die prematurely; competing with essential nutrients; binding to essential hormones; accumulating in organs that produce hormones.

Vaccines may cause the immune system to attack itself.

In what is called an autoimmune response — the fact aborted fetal cells are included in vaccines means the body could see healthy cells as hostile and then engage in self-destructive behavior.

Here is a video that suggests that nagalase is intentionally put into vaccines to weaken the immune system. Dr. Bradstreet found that autistic children tended to have a highly elevated level of nagalase in their blood. He claimed to have tested over 400 autistic children for the viral marker nagalase, and found that close to 80% of them had significantly elevated levels. This would make sense as part of a dumbing down and depopulation agenda as described in THRIVE (at 1:33:55). Bradstreet treated 1,100 patients with GcMAF, with an 85% response rate.

“GcMAF and/or oral Colostrum MAF macrophage activation therapy is indicated in the treatment of any diseases where there is immune dysfunction or where the immune system is compromised,” explains the website of a clinic out of Japan that sells an oral form of GcMAF.

Here’s a diagram of how GcMAF works:

What is GcMAF useful for?

One of the things that GcMAF does is kill a protein made by all cancer cells called nagalase, which is excreted by cancer cells to disarm the human immune system. Nagalase causes immunodeficiency

Besides cancer, the conditions listed as appropriate candidates for benefit from GcMAF treatment include:

  • Autoimmune diseases
  • Epstein-Barr Virus (EBV)
  • Hepatitis B virus (HBV)
  • Herpes Simplex virus (HSV)
  • Cystitis
  • Hepatitis C virus (HCV)
  • Multiple sclerosis (MS)
  • Urinary tract infection (UTI)
  • Autism Spectrum Disorders (ASD)
  • Rheumatoid arthritis (RA)
  • Endometriosis
  • Chronic Fatigue Syndrome (CFS)
  • Lyme disease (Lyme borreliosis)
  • IgA deficiency disorder
  • Myalgic Encephalomyelitis (ME)
  • Mycobacteria infections
  • Parkinson’s disease
  • Tuberculosis
  • Fibromyalgia
  • Human papillomavirus (HPV)
  • Lupus (Systemic lupus erythematosus, SLE)
  • Dengue fever
  • Pneumonia infection
  • Warts caused by viral infection
  • Norovirus
  • Malaria Influenza virus (flu)
  • Herpes simplex virus (HSV)
  • Q fever (Coxiella burnetii)
  • Polycystic ovary syndrome (PCOS)
  • Chicken pox (varicella zoster virus)
  • Psoriasis
  • Respiratory tract infections
  • Ulcerative colitis
  • Crohn’s disease
  • Type 1 diabetes (T1DM)
  • Insulin-dependent diabetes (IDDM)
  • Type 1.5 diabetes
  • Latent autoimmune diabetes of adults (LADA)

GcMAF is also showing itself to be effective for treating autism.

“In a study of 1500 children with autism, 85% had high levels of viruses and a compromised immune system. All 1500 received weekly GcMAF injections and 70% of the children responded to the treatment with reduced symptoms and another 15% made full recoveries. The other 15% did not respond. It was stated that the reduction of autistic symptoms is permanent provided that GcMAF has been taken long enough for the body to produce its own GcMAF which typically takes 24 weeks.”

I personally know individuals who have been dramatically helped by taking GcMAF. Marco Ruggerio delivered a paper at the AutismOne conference in May of 2015 — just before these murders started. Over the summer, patients who were using it had their supplies cut off from their original source in Switzerland where the company was being harassed and threatened. Subsequent shipments from another country were intercepted at the U.S. border, though eventually allowed through. Authorities in the UK have also been confiscating this beneficial compound.

Introducing foreign bodies via vaccination to instill a state of inflammation.

Text from James A. Miller

During the early 1990s, the World Health Organization (WHO) has been
overseeing massive vaccination campaigns against tetanus in a number
of countries, among them Nicaragua, Mexico, and the Philippines. In
October 1994, HLI received a communication from its Mexican
affiliate, the Comite Pro Vida de Mexico, regarding that country’s
anti-tetanus campaign. Suspicious of the campaign protocols, the
Comite obtained several vials of the vaccine and had them analyzed by
chemists. Some of the vials were found to contain human chorionic
gonadotrophin (hCG), a naturally occurring hormone essential for
maintaining a pregnancy.

hCG and anti-hCG antibodies.

In nature the hCG hormone alerts the women’s body that she is
pregnant and causes the release of other hormones to prepare the
uterine lining for the implantation of the fertilized egg. The rapid
rise in hCG levels after conception makes it an excellent marker for
confirmation of pregnancy: when a woman takes a pregnancy test she is
not tested for the pregnancy itself, but for the elevated presence of

However, when introduced into the body coupled with a tetanus toxoid
carrier, antibodies will be formed not only against tetanus but also
against hCG. In this case the body fails to recognize hCG as a friend
and will produce anti-hCG antibodies. These antibodies will attack
subsequent pregnancies by killing the hCG which naturally sustains a
pregnancy; when a woman has sufficient anti-hCG antibodies in her
system, she is rendered incapable of maintaining a pregnancy.[1]

HLI reported the sketchy facts regarding the Mexican tetanus vaccines
to its World Council members and affiliates in more than 60
countries.[2] Soon additional reports of vaccines laced with hCG
hormones began to drift in from the Philippines, where more than 3.4
million women were recently vaccinated. Similar reports came from
Nicaragua, which had conducted its own vaccination campaign in 1993.

The known facts.

Here are the known facts concerning the tetanus vaccination campaigns
in Mexico and the Philippines:

* Only women are vaccinated, and only the women between the ages of
15 and 45. (In Nicaragua the age range was 12-49). But aren’t men at
least as likely as young women to come into contact with tetanus? And
what of the children? Why are they excluded?

* Human chorionic gonadotrophin (hCG) hormone has been found in the
vaccines. It does not belong there -in the parlance of the O.J.
Simpson murder trial, the vaccine has been “contaminated.”

* The vaccination protocols call for multiple injections-three within
three months and a total of five altogether. But, since tetanus
vaccinations provide protection for ten years or more, why are
multiple inoculations called for?[3]

* WHO has been actively involved for more than 20 years in the
development of an anti-fertility vaccine utilizing hCG tied to
tetanus toxoid as a carrier-the exact same coupling as has been found
in the Mexican-Philippine-Nicaragua vaccines.[4]

The anti-fertility gang.

Allied with the WHO in the development of an anti-fertility vaccine
(AFV) using hCG with tetanus and other carriers have been UNFPA, the
UN Development Programme (UNDP), the World Bank, the Population
Council, the Rockefeller Foundation, the All India Institute of
Medical Sciences, and a number of universities, including Uppsala,
Helsinki, and Ohio State.[5] The U.S. National Institute of Child
Health and Human Development (part of NIH) was the supplier of the
hCG hormone in some of the AFV experiments.[6]

The WHO began its “Special Programme” in human reproduction in 1972,
and by 1993 had spent more than $356 million on “reproductive health”
research.[7] It is this “Programme” which has pioneered the
development of the abortificant vaccine. Over $90 million of this
Programme’s funds were contributed by Sweden; Great Britain donated
more than $52 million, while Norway, Denmark and Germany kicked in
for $41 million, $27 million, and $12 million, respectively. The
U.S., thanks to the cut-off of such funding during the Reagan-Bush
administrations, has contributed “only” $5.7 million, including a new
payment in 1993 by the Clinton administration of $2.5 million. Other
major contributors to the WHO Programme include UNFPA, $61 million;
the World Bank, $15.5 million; the Rockefeller Foundation, $2.5
million; the Ford Foundation, over $1 million; and the IDRC
(International Research and Development Centre of Canada), $716.5

WHO and Philippine Health Department excuses.

When the first reports surfaced in the Philippines of tetanus toxoid
vaccine being laced with hCG hormones, the WHO and the Philippine
Department of Health (DOH) immediately denied that the vaccine
contained hCG. Confronted with the results of laboratory tests which
detected its presence in three of the four vials of tetanus toxoid
examined, the WHO and DOH scoffed at the evidence coming from
“right-to-life and Catholic” sources. Four new vials of the tetanus
vaccine were submitted by DOH to St. Luke’s (Lutheran) Medical
Center in Manila-and all four vials tested positive for hCG!

From outright denial the stories now shifted to the allegedly
“insignificant” quantity of the hCG present; the volume of hCG
present is insufficient to produce anti-hCG antibodies.

But new tests designed to detect the presence of hCG antibodies in
the blood sera of women vaccinated with the tetanus toxoid vaccine
were undertaken by Philippine pro- life and Catholic groups. Of
thirty women tested subsequent to receiving tetanus toxoid vaccine,
twenty-six tested positive for high levels of anti-hCG antibodies! If
there were no hCG in the vaccine, or if it were present in only
“insignificant” quantities, why were the vaccinated women found to be
harboring anti-hCG antibodies? The WHO and the DOH had no answers.

New arguments surfaced: hCG’s apparent presence in the vaccine was
due to “false positives” resulting from the particular substances
mixed in the vaccine or in the chemicals testing for hCG. And even if
hCG was really there, its presence derived from the manufacturing

But the finding of hCG antibodies in the blood sera of vaccinated
women obviated the need to get bogged down in such debates. It was no
longer necessary to argue about what may or may not have been the
<cause> of the hCG presence, when one now had the <effect> of the
hCG. There is no known way for the vaccinated women to have hCG
antibodies in their blood unless hCG had been artificially introduced
into their bodies!

Why a tetanus toxoid “carrier”?

Because the human body does not attack its own naturally occurring
hormone hCG, the body has to be fooled into treating hCG as an
invading enemy in order to develop a successful antifertility vaccine
utilizing hCG antibodies. A paper delivered at the 4th International
Congress of Reproductive Immunology (Kiel, West Germany, 2629 July
1989) spelled it out: “Linkage to a carrier was done to overcome the
immunological tolerance to hCG.”[8]

Vaccine untested by Drug Bureau.

After the vaccine controversy had reached a fever pitch, a new
bombshell exploded: none of the three different brands of tetanus
vaccine being used had ever been licensed for sale and distribution
or registered with the Philippine Bureau of Food and Drugs (BFAD), as
required by law. The head of the BAFD lamely explained that the
companies distributing these brands “did not apply for
registration.”[9] The companies in question are Connaught
Laboratories Ltd. and Intervex, both from Canada, and CSL
Laboratories from Australia.

It seemed that the BAFD might belatedly require re-testing, but the
idea was quickly rejected when the Secretary of Health declared that,
since the vaccines had been certified by the WHO -there they are
again!-there was assurance enough that the “vaccines come from
reputable manufacturers.”[10]

Just how “reputable” one of the manufacturers might be is open to
some question. In the mid-’80s Connaught Laboratories was found to
be knowingly distributing vials of AIDS-contaminated blood


At this juncture, evidence is beginning to appear from Africa.[12]
HLI has called for a Congressional investigation of the situation,
inasmuch as nearly every agency involved in the development of an
anti-fertility vaccine is funded, at least in part, with U.S.


1 “Abortifacient vaccines loom as new threat,” <HLI Reports>,
November 1993, pp. 1-2.

2 <World Council Reports>, 28 November 1994, pp. 4-5.

3 A call placed by this writer on 5 May 1995 to the Montgomery County
(Maryland) Health Department, Epidemology Division-Infectious
Diseases – Adult Immunizations, elicited the following information:

Q. For how long a time does the tetanus vaccination offer protection?

A. 10 years.

Q. Have you ever heard of any adult requiring three tetanus
vaccinations within a 3 or 4 month time period, and a total of 5
vaccinations in all within a year or so?

A. Whaaaat! Never. No way!

Reports from the Philippines appear to confirm the 10-year immunity
afforded by tetanus toxoid vaccinations: prior to the campaigns begun
in 1993, the so-called booster shots were given only every 10-years.

4 More than a score of articles, many written by WHO researchers,
document WHO’s attempts to create an anti-fertility vaccine utilizing
tetanus toxoid as a carrier. Some leading articles include:

“Clinical profile and Toxicology Studies on Four Women Immunized with
Pr-B-hCG- TT,” <Contraception>, February, 1976, pp. 253-268.

“Observations on the antigenicity and clinical effects of a candidate
antipregnancy vaccine: ,B-subunit of human chorionic gonadotropin
linked to tetanus toxoid,” <Fertility and Sterility>, October 1980,
pp. 328-335

“Phase I Clinical Trials of a World Health Organization Birth Control
Vaccine,” <The Lancet>, 11 June 1988, pp. 1295-1298. “Vaccines for
Fertility Regulation,” Chapter 11, pp. 177-198, <Research in Human
Reproduction, Biennial Report> (1986-1987), WHO Special Programme of
Research, Development and Research Training in Human Reproduction
(WHO, Geneva 1988).

“Anti-hCG Vaccines are in Clinical Trials,” <Scandinavian Journal of
Immunology>, Vol. 36, 1992, pp. 123-126.

5 These institutional names are garnered from the journal articles
cited in the previous footnote.

6 <Lancet>, 11 June 1988, at p. 1296.

7 <Challenges in Reproductive Health Research, Biennial Report
1992-1993>, World Health Organization, Geneva, 1994, p. 186.

8 G.P. Talwar, et al, “Prospects of an anti-hCG vaccine inducing
antibodies of high affinity…(etc),” <Reproductive Technology> 1989,
Elsevier Science Publishers, 1990, Amsterdam, New York, p. 231.

9 3 DOH vaccines untested by BFAD,” <The Philippine Star>, 4 April
1995, pp. 1, 12.

10 “BFAD junks re-testing of controversial shot,” <Manila Standard> 7
April 1995; “DOH: Toxoid vaccines are safe,” <The Philippine Star>. 7
April 1995.

11 “Ottawa got blood tainted by HIV.” <Ottawa Citizen>, 4 April 1995.

12 A nearly two-year old communique from Tanzania tells a familiar
story: tetanus toxoid vaccinations, five in all, given only to women
aged 1545. Nigeria, too, may have been victimized; see <The Lancet>,
4 June 1988, p. 1273.
Taken from the June/July 1995 issue of “HLI Reports.” To subscribe
contact: HLI Reports, 7845 Airpark Road, Suite E Gaithersburg, MD

Inflammatory Disease Epidemic: The Convergence Point of EMF, GMOs, and Vaccines

Article from Dr. Matthew Buckley, PSc.D, CTTH from Kinseimindbody

The US spends more per capita on healthcare than any other nation on the planet(R), at over $1 Trillion/year with costs growing.   Over 3/4 of those costs are related to the treatment of chronic disease, such as autoimmune disorders, cancer, diabetes, alzheimers, autism, cadiovascular disease, etc.(R)  The rates of all such diseases are growing, not decreasing, so obviously the true causes of these problems aren’t being addressed.   If you were to try and describe virtually all forms of degenerative disease with just one word, that word would be “inflammation”(R)  The research is very clear about this fact.  When examining the prime factors behind the surge in inflammatory issues there are principally 3 things that stand out as different about today versus 25 years ago.  Those 3 things are the widespread consumption of RoundUp laden genetically modified food and wheat (R)(R), wireless technology (R), and a surge in the number of vaccines given relative to years past (R).   The biological effects of each of these technologies is understood well enough to help put the pieces together and begin to understand how their effects may work synergistically to promote the chronic inflammatory disease epidemic we’re firmly in.

Monsanto’s RoundUp Fuels Alterations in Our Gut Ecology, And These Alterations Can Inflame Our Nervous System.

In a previous blog post, “Synergistic Destruction: How Vaccines and GMOs Converge to Fuel Autism and Neurodegenerative Disorders“, I provided a heavily referenced explanation for key factors driving neurodegenerative conditions with a particular emphasis on autism.  The gist of the article is that genetically modified food, through its contamination of Monsantos roundup residue was leading to gut flora alterations(R)(R)(R) which break down the gut barrier (leaky gut) initiating inflammatory processes within the brains of susceptible individuals.  The fire embers of leaky gut driven brain inflammation could then ignite into significant and persistent brain inflammation through the introduction of vaccines and express its effects in much of what is seen in autism, alzheimers, ALS, MS, Parkisons, etc.  It is recommended that you first read that post before reading this.

Microglial Activation is a more descriptive term used to describe immune system activated inflammation of the nervous system.  In short, it refers to how the microglia, the resident immune cells of the nervous system, shift from a beneficial state of surveillance and repair, into a state of breakdown and inflammatory destruction.  They do this through the excessive release of destructive immune messaging molecules (cytokines) and excitatory neurotransmitters (glutamate).   The fulcrum by which these cells shift from the beneficial to the noxious state rests upon the ability of the cells to maintain adequate amounts of the chemical called glutathione.   All cells produce glutathione, but maintaining optimal levels can be a challenge for various reasons including, genetics, nutrient status, toxic body burden, and gut flora health.  As glutathione levels wane, the immune cells both within the periphery of the body and within the nervous system tip the fulcrum of balance towards inflammatory destruction.(R)

Melatonin:  The Premier Protective Molecule of Our Body is Depleted By Modern Technology. 

In a recent blog post, (advisable to also read first), about the many biochemically important functions of melatonin, I describe how melatonin is a key which turns on a cellular switch called “NRF2” that triggers cellular production of many key antioxidants, including glutathione.   In addition, you’ll see that altered gut ecology driven in part by Monsantos RoundUp residue can compromise production of melatonin.   This compromise in production is further hindered by fluoridated water calcifying the melatonin producing pineal gland(R), night time artificial light exposure (R), and what is produced is being burned up through the overproduction of free radicals upon exposure to the sea of electromagnetic wireless radiation we commonly find ourselves immersed in.

Research strongly suggests that EMF exposure generates excessive peroxynitrite (R), a potently destructive free radical, and peroxynitrite is scavenged by antioxidants including melatonin.   Upon on examination of the volumes of research evaluating the protective and antiaging effects of melatonin, it is no exaggeration to call it our bodies premier protective molecule.   Big pharma knows all about this which is why they’re working on developing drugs modeled around a similar, chemically distinct, altered form of melatonin that they can patent.(R)

Here’s where things get more interesting.

When examining inflammatory, especially autoimmune, disorders there is a wing of the immune system cells that are overexpressed or under suppressed.  The expression is shaped by the immune messaging molecules called “cytokines”.  Different cytokines lead to different branches of immune system expression. The immune system was once thought to be divided into TH1/TH2 balance, where TH 1 is principally characterized as the immune defense within the cells and TH2 as immune defense outside of the cells.  More current research now recognizes another subset of immune cells called TH 17 that appears to be the most destructive component of the immune system when it’s not brought into balance.  You’ll find the proinflammatory TH 17 elevations in autism(R), alzheimers (R), ALS (R), cancer (R), cardiovascular disease (R) Crohns disease (R), Hastimotos thyroidits (R), Graves Disease (R), MS (R), Parkisons (R), rheumatoid arthritis (R), lupus (R), psoriasis (R), seasonal allergies (R), and likely every other autoimmune disorder that exists.

TH17 function is important in immune system memory and helping our bodies to eliminate certain types of infections, but when the body isn’t able to turn down this component of the immune system the cells literally become wrecked through persistent inflammation.  It is very important to note here that vaccines are known initiators of TH17 activity, and this activity through the introduction of various pathogens, not to mention adjuvants (additives within vaccines), may drive persistent TH1/TH17 activation.(R)

How all of this relates to melatonin is that a recent study titled, “Melatonin Lulling TH 17 Cells to Sleep“,  published in the journal “Cell” describes how melatonin turns the key cellular switch to dampen an overproduction of TH 17 cells.  The authors of that study go on to state,  

“Over the past 50 years, there has been a steady rise in the incidence of autoimmune diseases such as MS, RA, psoriasis, and IBD, particularly in developed countries. Recent studies have uncovered many environmental stress factors associated with the modern life contributing to the development of inflammatory disorders… It is tempting to speculate whether the invention of artificial lights—which facilitates chronic circadian disruptions—could have contributed to an imbalance between the inflammatory and regulatory responses of the immune system, leading to immune dysregulation.  The current study establishes a clear link between melatonin, a hormone involved in the regulation of the circadian rhythm, and the inhibition of proinflammatory Th17 cells, thereby shifting the balance of the immune response toward immunosuppression.”

Good health is all about balance. 

While many people think that immune system function is all about “boosting” function in terms of maintaining health, the reality is that it’s about maintaining proper balance within the immune system.  Too much immune system response is characterized by autoimmune disorders of persistent inflammation which extends beyond the presence of a pathogen within a tissue on the TH1 end, or environmental allergies on the TH2 end, particularly when coupled with elevations of TH17 on either end.  Too little immune system function is characterized by infections or metastatic cancers consuming the body.  What we want to achieve is balance, and that balance is principally maintained by producing adequate numbers of T Regulatory cells and keeping TH 17 overproduction in check.  Not only does melatonin suppress overproduction of the TH 17 cells, it increases the production of T regulatory cells which also keep overreactive sides of both TH1/TH2 in check.(R)  Research shows that maintaining glutathione levels helps to maintain adequate numbers of T regulatory cells(R), and as I pointed out, it is melatonin that serves as our bodies primary key in turning on glutathione synthesis via NRF2 stimulation.  As I said, melatonin is our bodies premier protective molecule.  The end result of persistently low melatonin is increased toxicity and increased inflammation, exactly what you don’t want when you consume toxins within food, or are injected with inflammation inducing vaccines.  Noteworthy and common nutrient deficiencies which can combine to directly worsen this imbalance include vitamins A, D, and selenium.(R)(R)(R)


In summary:

It begins in the gut.  Alterations within the gut flora are occurring in large part through the consumption of RoundUp residue in genetically modified food, not to mention sugar/HFCS processed food and overly prescribed antibiotics.  This gut flora alteration is commonly characterized by an overgrowth of pathogenic bacteria which break down the lining of the gut.  Furthermore, the gut flora alterations then compromise the ability for the body to make the raw ingredients for melatonin production, namely tryptophan and serotonin.  The lining of the gut is maintained, in part, by melatonin(R).  As the microbes and their waste products seep into the blood stream the immune system within the periphery of the body releases inflammatory molecules which begin to promote proinflammatory activity in the nervous system.  This proinflammatory activity state is called, microglial activation.  The microglial cells being the primary immune cells of the nervous system are prone to shifting from a beneficial state of repair and surveillance into a destructive state of inflammation when they lack adequate amounts of glutathione.   Likewise, glutathione also plays an important role in maintaining adequate levels of T regulatory cells which help to prevent excessive production and response of the immune system.  It is melatonin which turns the switch on  for cellular glutathione production via a cellular switch called NRF2, and thus not only plays an important role in preventing and repairing leaky gut, but also prevents the immune system from shifting into a destructive and proinflammatory state systemically.

The preceding paragragh serves as the biochemical background for millions of Americans right now.   We can all recognize that not all people quickly succumb to rapid adverse reactions to vaccines.  Some do, which is why over $2 Billion have been awarded in the “vaccine court”(R), as those cases are easier to prove clear cause and effect damage in comparison to those injured months or years later by vaccines (R).   It is my contention that the stage for adverse reactions to vaccines is driven by an immune system which has been primed for persistently significant inflammation by those factors which upregulate the TH17 wing of the immune system.  The recent shift within the healthcare system to recommend mercury laden flu vaccines to pregnant women (R) is sure to fuel a greater epidemic of chronic illness as research demonstrates that “intrauterine adversity, characterized by toxicity, can fuel a lifetime of TH17 destructive and proinflammatory behavior“.(R)

The only way to avoid the worsening of the catastrophe of chronic illness is through education and action.  This isn’t a call for an Amish revolution.  The reality is that we don’t need GMO food to feed the world, and the frequencies being used with wireless technology could, in theory, be replaced with health promoting frequencies, or fiber optic connections.  Likewise, if you believe in vaccination, I’m not against taking that right away from you, nor am I overly concerned with the fact that, upon receiving your vaccine, you may be spreading the pathogens which you believe you’re being protected from.(R)(R) However, if you really believe in vaccines, you shouldn’t have anything to fear from the unvaccinated population, right?

buckley-feb2013-0021About the author:  Dr. Buckley is a 2002 graduate of Logan College of Chiropractic.  He entered the health care field largely to understand and resolve his personal struggles with chronic fatigue and fibromyalgia which began late in his teens.  His ongoing study of functional medicine, nutrition, nutrigenomics, applied kinesiology, and energetic medicine has provided him with keen insight and understanding into the holistic dynamics of the body and how we lose and maintain our health.  He has maintained a busy practice in Austin, Texas for the past 13 years and works with people of all ages interested in maximizing their health, and overcoming the modern scourge of all forms of chronic illness.