New Research Proves Brains of Children with Autism are Loaded with Aluminum

Recent research undertaken by Professor Christopher Exley and his team from Keele University in Staffordshire leaves parents with little doubt that aluminum plays a crucial part in the brain tissue of individuals with autism.

For the very first time, Exley and his team had the unique opportunity to examine the brain tissue of individuals who had died with a diagnosis of autism. and what they discovered was truly shocking. Their study determined that the brain tissue of individuals who had died with a diagnosis of autism contained the highest levels of aluminum of any other brain tissue that had been examined by the team.

In a video released on November 29, 2017, Exley explained his findings. He stated that:

“We were able to do two things, we were able to measure how much aluminum was in the brain in individuals who had died with autism, and we also able to look at the aluminum in the tissue using a microscopy technique called fluorescence. The amount of aluminum in the brain tissue was, I would say extraordinarily high.” [1] (own emphasis)

The results of their study shocked the team because, over the years. they had examined the brain tissue of well over one hundred individuals and, according to Exley, the brain tissue of the individuals who had died with a diagnosis of autism contained the highest levels of aluminum that the team had ever seen.

Exley explained that the only brains that he had seen containing similar amounts of aluminum were the brains of the patients who had died with a diagnosis of familial Alzheimer’s disease. [2]

He stated that:

“In this relatively young group of people, some thirteen, fourteen, fifteen years of age, we saw more aluminum than we had seen in other circumstance.”

Exley’s statement is truly shocking, especially when you consider that he and his team had previously been examining the brain tissue of more senior patients who had died of Alzheimer’s disease. You would expect to find that individuals who died in their seventies and eighties would have a far greater concentration of aluminum in the brain than those who had died at the tender age of thirteen.

Exley continued by revealing that:

“Perhaps equally important if not more important were the microscopy studies. Microscopy studies enabled us to identify where the aluminum was in the brain tissue. When we looked at the brains of people with a diagnosis of autism, we found something completely different, something we have never seen before, as yet in any other set of human brains. We found that the majority of aluminum was actually inside the cells, ‘intracellular.’”

He explained that these cells were carrying with them a cargo of aluminum from the body into the brain. He stated that:

“We also saw evidence that cells in the lymph and in the blood were passing into the brain, so they were carrying with them a cargo of aluminum from the body into the brain. This is the first time in any brain tissue that we have seen, so this is a stand out and as yet unique observation in autism.”

This leads us to question, where the aluminum was coming from?

We Are Being Bombarded with Aluminum Every Day

As many of us are aware, we are living in what Exley calls “the age of aluminum.” The human body is being bombarded with aluminum in everyday products. For example, many of our foods, vaccinations, medications, baby products, cosmetics, cleaning products and even soft furnishings contain aluminum, and it appears that we are powerless to prevent the ever-increasing onslaught.

However, despite the fact that aluminum is known to be a toxic substance and, according to the New Jersey Department of Health and Senior Services, a potential health hazard, aluminum has been named as the second most used metal in the world after steel, largely due to its versatility. [3]

Exley Now Concerned About the Aluminum Content in Vaccines

Before embarking on this study, Exley had believed that there was no safe alternative to aluminum as an adjuvant in vaccinations. However, since studying the aluminum/autism link he has had a change of heart.

He explained that:

“Because I have seen the same cells from the ones seen at the injection site carrying a cargo of aluminum into the brain tissue of individuals who have died of autism, I would now say we have to think very carefully about who receives a vaccine which includes an aluminum adjuvant.
We have to think carefully, is this vaccine a life saving vaccine or not? If it isn’t, don’t have it with an aluminum adjuvant.”

 

To read Professor Exley’s peer-reviewed study on aluminium in brain tissue in autism, see reference [4].

Exley’s study was funded in part by the Children’s Medical Safety Research Institute (CMSRI), an organization whose members have believed for many years that aluminum has been the cause of neurological disorders. On their website, they have stated that:

“The Children’s Medical Safety Research Institute, also known as CMSRI was established to provide funding for research to address eroding national health, particularly in very young and elderly populations. Concerns have been raised by the scientific community about the acknowledged significant increases in immune, inflammatory and cognitive disorders in children and adults ranging from asthma and neurodevelopmental disorders to the emergence of previously rare but serious autoimmune health conditions and age related disorders in the nervous system during the past three decades.”

They continued:

“The effect of vaccines on the immune and neurological systems must also be assessed in association with cognitive function as it is related to academic performance and systemic effects on the educational system. As schools enforce government vaccine policies, a valid assessment of impact will support future decisions about public health policies as they relate to school policies.” [5]

In reality, Exley’s suggestion to only vaccinate with a vaccination containing an aluminum adjuvant if it is completely necessary is easier said than done. According to research, vaccinations containing aluminum have only been added to the childhood immunization schedule when some vaccines containing mercury were removed and the number of vaccines containing this adjuvant appears to be increasing every year.

In his paper, Aluminum in Childhood Vaccines is Unsafe, Neil Z. Miller wrote that:

“Prior to the mercury phase-out (pre-2000), babies received 3,925 mcg of aluminum by 18 months of age. After pneumococcal and hepatitis, A vaccines were added to the schedule, babies began receiving 4,925 mcg of aluminum during the same age period—a 25% increase.” [6]

This is a massive increase and if true, it is hardly surprising that it is affecting the brain tissue of children.

Miller demonstrated exactly how much aluminum children were receiving through vaccination by using a series of charts. He wrote:

“Age-Specific and Cumulative Aluminum Exposure by 18 Months of Age

  • Birth 250 mcg aluminum
  • 2 months 1225 mcg aluminum
  • 4 months 975 mcg aluminum
  • 6 months 1000 mcg aluminum
  • 12 months 600 mcg aluminum
  • 15 months 623 mcg aluminum
  • 18 months 250 mcg aluminum”

As you can see, a baby receives a total of 4,925 mcgs of aluminum by the time they are 18 months of age, from vaccinations alone.

Miller concluded that:

“Toxic metals such as aluminum do not belong in prophylactic medications administered to children, teenagers, or adults. Vaccines are normally recommended for healthy people, so safety (and efficacy) standards must be impeccable. Parents, especially, should not be compelled to permit their loved ones to receive multiple injections of toxic metals that could increase their risk of neurodevelopmental and autoimmune ailments. Safe alternatives to current disease prevention technologies are urgently needed.”

Exley’s recent research appears to support Miller’s findings, and, as Miller stated, “toxic metals such as aluminum do not belong in prophylactic medications administered to children, teenagers, or adults.”

In an interview, I asked Professor Exley the following questions:

England: It has been thought for many years that thimerosal was responsible for causing autism; does your study put doubt on this as a theory?

Exley: No, since we have not researched mercury.

England: In your opinion, could autism be a childhood form of Alzheimer’s disease?

Exley: Actually, this thought has crossed my mind!

England: It appears that one way or another, aluminum could be responsible for neurological disorders to occur; why do you think that they manifest in so many different ways?

Exley: The result of aluminum toxicity is simply down to where and how it accumulates in human tissue. It is so biologically-reactive that it can disrupt many, many biochemical pathways. However, for this disruption to manifest as disease the number and severity of the disruptions must increase above a tolerable threshold and to achieve this threshold you need time (e.g. in AD) or unusual circumstances (as may be the case in autism).

His answers are concerning, because if he is correct, every child who has received a vaccine containing aluminum is at risk from becoming ill. This is because no one knows exactly what level of aluminum is safe.

What Can Parents Do to Help Their Children?

This news is extremely worrying for parents. However, there is one thing that every parent can do to protect their child and that is to reduce their body burden of aluminum in any way that they can.

One way that has been proven to help reduce the body burden of aluminum is by drinking a silicon-rich mineral water every day.

What are Silicon-Rich Mineral Waters?

Natural, silicon-rich mineral water differs significantly from many other alternative bottled waters, as it naturally contains more silicon in the soluble form (known as silica acid) than most. This is because silica is naturally occurring and not synthetically produced. What is even more interesting is the fact that silica acid is the only form of silicon that humans can effectively digest and absorb into the body’s system.

Silicon-rich mineral waters are sourced from natural aquifers buried deep below the tropical rain forest and hidden away from all pollution to protect them from the outside world. Silica, a mineral that is abundant in silica water, is naturally occurring as the result of natural chemistry which takes place deep underground and cannot be synthetically reproduced. This is because only nature has the power to create the unique qualities of silica water.

While supermarkets now stock a wide range of bottled waters, only a few of them contain silica. Of the brands that do contain silica, only three of them can truly be classified as silicon-rich, defined as 30 parts per million (ppm) of silica or above.

Although there are many mineral waters that contain silica, until recently, there have only been three main silicon-rich mineral waters available: Spritzer, Volvic and Fiji, which contain the required 30 ppm of silica or above.

However, this situation has now changed, because on January 24, 2017, the Malaysian company Spritzer launched Acilis, which is sold in the United Kingdom and Europe.

In an article published in the Hippocratic Post, titled Why everyone should drink a silicon-rich mineral water, Professor Exley wrote:

“What we have found in clinical trials, involving both healthy individuals and individuals with disease, is that drinking around a litre of silicon-rich mineral water every day can speed up the removal of toxic aluminium from the body via the kidneys and ultimately urine. In fact, our studies showed that individuals experienced significant reductions in their body burden of aluminium, including falls of up to 70% in one case, over a 12-week period.

Silicon-rich mineral waters help to remove aluminium from the body because they are actually rich in soluble silicon or silicic acid. This form of silicon immediately follows water molecules through the gut wall and into the bloodstream where it forms a complex with aluminium called an hydroxyaluminosilicate. This form of aluminium can be easily filtered from the blood by the kidney. Hence, silicon-rich mineral waters increase the excretion of aluminium in the urine.” [7]

If he is correct, then this leads us to question whether or not it is possible that drinking a silicon-rich mineral water on a regular basis could benefit children with autism.

Parents Say Their Autistic Children Improved After Drinking Acilis

The answer appears to be yes, because interestingly, there are two testimonials on the Acilis website from parents stating that their autistic children have improved after drinking Acilis silicon-rich mineral water on a regular basis.

Testimonial 1

“After just 2 weeks of drinking Acilis water, I have already seen amazing results with my 2-year-old autistic daughter who has shown increased eye contact, better non-verbal communication and increased pre-verbal sounds. And to my delight called me ‘Mamma’ for the very first time in her tiny life.

You have no idea how much this means to us as parents. We have a battle that we have to fight with NHS and Local Authorities to get services and help for our children, which they just do not want to do, and then there are conscious minded companies like yours which provide a lifeline for parents like us.” [8]

Testimonial 2

“Wow what a huge difference Acilis has made for my autistic children. My 16 years old has suffered with severe constipation most of his life, this water has made his life so much more bearable as it has helped him relieve himself without the use of medication.

My 6-year-old has also showed positive signs in learning. It is just amazing that something so simple as water can do such wonders. I really want to continue this wonderful water for my children as it has helped them so much.” [9]

According to Rex Garratt, Spritzer’s UK distributor and founder of the Acilis website, these testimonials were placed on the Acilis website long before Exley’s study on aluminum and autism was published.

If he is correct, then this fact alone proves that Professor Exley’s study is correct and aluminum is linked to autism.

 

References

  1. https://www.youtube.com/watch?v=SmkVv8pcVhc 
  2. http://www.sciencedirect.com/science/article/pii/S0946672X16303777
  3. http://www.nj.gov/health/eoh/rtkweb/documents/fs/0054.pdf
  4. http://www.sciencedirect.com/science/article/pii/S0946672X17308763
  5. http://www.cmsri.org/about/
  6. http://www.jpands.org/vol21no4/miller.pdf
  7. https://www.silicawaters.com/
  8. https://www.silicawaters.com/mothers-testimonial…
  9. https://www.silicawaters.com/wow…
About the author

Christina England, BA Hons

  • Anna Watson

    A very clear, well written article. I trust that Prof. Exley is afforded respect in the science world while they try to replicate his findings. For those already vaccinated, silica rich water may help which is promising, although I hope that parents will look again at the risk v benefit scenario for vaccination with ALU toxicity in mind.

  • Karl Wegner MD

    The results are meaningless without controls. Typical antivax research.

  • Really, you mindlessly and repeated say that about every truly damning vaccine study that has ever existed. People with autism donated their brains to science, and the study contained the resulting findings. The brain of normal individuals did not and does not contain those levels of aluminum. Where else is the aluminum coming from if not injected aluminum adjuvants in vaccines. Perhaps you should actually review what was found in the study. And stop using the faked and the false MD identity of someone that is deceased.

    Christopher Exley is one of the foremost experts on aluminum and aluminum toxicity within the human body. Listen as he explains and describes the results of his recent aluminum adjuvant related vaccine study, with co-authors!!!
    https://www.youtube.com/watch?time_continue=6&v=SmkVv8pcVhc

    The Toxicity of Aluminum Adjuvants
    Christopher Exley
    https://www.youtube.com/watch?v=zaExaqCv5vo

    Dr. Exley on Vaccines, PhD in Ecotoxicology of Aluminum, University of Stirling
    https://www.youtube.com/watch?v=il6wH81qHAo

    Christopher Exley, more informational videos on aluminum toxicity.
    https://www.youtube.com/results?search_query=Christopher+Exley+aluminum+study+

    Study: Record Levels of Aluminum Found in Autistic Children Brain Tissue

    November 28, 2017 4:04 pm

    11-27-Aluminum_Featured_Image-300×156
    Dr. Christopher Exley—one of the world’s leading experts on aluminum toxicity—has shown that chronic intoxication with myriad forms of this “ubiquitous and omnipresent metal” is exacting a high price on human health. Dr. Exley and other aluminum experts such as molecular biologist Dr. Lucija Tomljenovic have confirmed that aluminum readily and actively traverses the blood-brain barrier to selectively accumulate in brain tissues, where it induces unwelcome changes in brain biochemistry. As Dr. Exley has noted, “There are no ‘normal’ levels of brain aluminum,” meaning that “its presence in brain tissue, at any level, could be construed as abnormal” In light of the fact that even minute amounts of aluminum can have adverse neurological consequences, Dr. Exley’s newest paper—which reports on the first-ever study of aluminum in ASD brain tissue—is groundbreaking. Published in the Journal of Trace Elements in Medicine and Biology, the paper documents some of the highest values for aluminum in human brain tissue ever recorded. Using a two-pronged study design, the researchers measured and characterized aluminum deposits in brain tissues from five to ten ASD donors, most of whom died in their teens or twenties. What the research team found was startling. The study’s quantitative arm documented “consistently high” aluminum levels representing “some of the highest values for brain aluminum content ever measured in healthy or diseased tissues.”

    Read More…
    http://vaccineimpact.com/2017/study-record-levels-of-aluminum-found-in-autistic-children-brain-tissue/

    Aluminium in brain tissue in autism

    Abstract
    Autism spectrum disorder is a neurodevelopmental disorder of unknown aetiology. It is suggested to involve both genetic susceptibility and environmental factors including in the latter environmental toxins. Human exposure to the environmental toxin aluminium has been linked, if tentatively, to autism spectrum disorder. Herein we have used transversely heated graphite furnace atomic absorption spectrometry to measure, for the first time, the aluminium content of brain tissue from donors with a diagnosis of autism. We have also used an aluminium-selective fluor to identify aluminium in brain tissue using fluorescence microscopy. The aluminium content of brain tissue in autism was consistently high. The mean (standard deviation) aluminium content across all 5 individuals for each lobe were 3.82(5.42), 2.30(2.00), 2.79(4.05) and 3.82(5.17) μg/g dry wt. for the occipital, frontal, temporal and parietal lobes respectively. These are some of the highest values for aluminium in human brain tissue yet recorded and one has to question why, for example, the aluminium content of the occipital lobe of a 15 year old boy would be 8.74 (11.59) μg/g dry wt.? Aluminium-selective fluorescence microscopy was used to identify aluminium in brain tissue in 10 donors. While aluminium was imaged associated with neurones it appeared to be present intracellularly in microglia-like cells and other inflammatory non-neuronal cells in the meninges, vasculature, grey and white matter. The pre-eminence of intracellular aluminium associated with non-neuronal cells was a standout observation in autism brain tissue and may offer clues as to both the origin of the brain aluminium as well as a putative role in autism spectrum disorder.

    https://www.sciencedirect.com/science/article/pii/S0946672X17308763

    Full study: (scroll down on page)
    https://ac.els-cdn.com/S0946672X17308763/1-s2.0-S0946672X17308763-main.pdf?_tid=f2be2fde-d56d-11e7-9e32-00000aab0f27&acdnat=1512005566_4d3d686804922e47e0b559810404e854

    New Study: 10x more aluminum in brains with autism

    From our friends at the Children’s Medical Safety Research Institute

    Discovery of “Shockingly High” Levels of Aluminum in Brains of Individuals with Autism Suggests Link with Aluminum-Containing Vaccines

    STAFFORDSHIRE, UNITED KINGDOM–(Marketwired – November 28, 2017) – A new study published in the Journal of Trace Elements in Medicine and Biology provides the strongest indication yet that aluminum is an etiological agent in autism spectrum disorder (ASD), according to researchers at Keele University in England.

    The study used transversely heated graphite furnace atomic absorption spectrometry to measure, for the first time, the aluminum content of brain tissue from five donors who had died with diagnoses of ASD. The results showed the donors to have had some of the highest values of aluminum yet measured in human brain tissue.

    The mean (standard deviation) aluminum content across all five individuals for each lobe were 3.82(5.42), 2.30(2.00), 2.79(4.05) and 3.82(5.17) mg/g dry wt. for the occipital, frontal, temporal and parietal lobes respectively. Previous measurements of 60 brains from humans not diagnosed with ASD showed an average content of 1 mg/g dry wt. of brain tissue.

    “One has to wonder why aluminum in the occipital lobe of a 15-year-old boy with autism would be a value that is at least 10 times higher than what might be considered acceptable for an elderly adult?” said Christopher Exley PhD, Professor in Bioinorganic Chemistry and author of the study. Another ground-breaking study by Exley and his team, published earlier in the year, identified similarly high levels of aluminum in the brains of individuals who died of familial Alzheimer’s disease.

    While the aluminum content of each of the five brains was extraordinarily high, it was the location of the aluminum in the brain tissue that served as the standout observation. The majority of aluminum was identified inside non-neuronal cells including microglia and astrocytes. Aluminum was also found in lymphocytes in the meninges and in similar inflammatory cells in the vasculature. According to the researchers, there was clear evidence of inflammatory cells heavily loaded with aluminum entering the brain via the meningeal membranes and the blood-brain-barrier.

    Aluminum-selective fluorescence microscopy was used to identify aluminum in the brain tissue of 10 donors. The results strongly suggest that aluminum is entering the brain in ASD via pro-inflammatory cells which have become loaded up with aluminum in the blood and/or lymph, much as has been demonstrated for monocytes at injection sites for vaccines including aluminum adjuvants.

    The fact that the majority of aluminum found in brain tissues in ASD was intracellular and associated with non-neuronal cells is, at least for now, unique to ASD and may begin to explain why young adolescents had so much aluminum in their brains.

    “The research does not infer that Al is a cause of autism, “said Exley, who also authored Human Exposure to Aluminum. “But these very high concentrations of a neurotoxin in brain tissue are not going to be benign and will contribute to neurodegeneration in affected tissues.”

    This study was funded by the Children’s Medical Safety Research Institute, a 502(c)3 nonprofit organization dedicated to funding independent research into the causal factors behind today’s epidemic of childhood chronic illness and disability.

    Access to the full article here:
    https://www.sciencedirect.com/science/article/pii/S0946672X17308763

    November 28, 2017 07:00 ET
    Discovery of “Shockingly High” Levels of Aluminum in Brains of Individuals with Autism Suggests Link with Aluminum-Containing Vaccines
    http://www.marketwired.com/press-release/discovery-shockingly-high-levels-aluminum-brains-individuals-with-autism-suggests-link-2241940.htm

    Big Pharma and Big Profits: The Multibillion Dollar Vaccine Market – New Report says “Vaccine Market” Worth $61 Billion by 2020
    https://www.globalresearch.ca/big-pharma-and-big-profits-the-multibillion-dollar-vaccine-market/5503945

    Children’s Medical Safety Research Institute,

    Global study research
    http://www.cmsri.org/global-research/

    CMSRI-funded Research
    http://www.cmsri.org/cmsri-funded-research/

    J Inorg Biochem. 2011 Nov;105(11):1489-99. doi: 10.1016/j.jinorgbio.2011.08.008. Epub 2011 Aug 23.
    Do aluminum vaccine adjuvants contribute to the rising prevalence of autism?
    Tomljenovic L1, Shaw CA.
    https://www.ncbi.nlm.nih.gov/pubmed/22099159

    Aluminum?s Role in CNS-immune System Interactions leading to Neurological Disorders
    https://www.omicsonline.org/open-access/aluminums-role-in-cnsimmune-system-interactions-leading-to-neurological-disorders-14822-1745-7580-9-069.php?aid=20403

    Immunol Res. 2013 Jul;56(2-3):304-16. doi: 10.1007/s12026-013-8403-1.
    Aluminum in the central nervous system (CNS): toxicity in humans and animals, vaccine adjuvants, and autoimmunity.
    Shaw CA1, Tomljenovic L.

    Abstract
    We have examined the neurotoxicity of aluminum in humans and animals under various conditions, following different routes of administration, and provide an overview of the various associated disease states. The literature demonstrates clearly negative impacts of aluminum on the nervous system across the age span. In adults, aluminum exposure can lead to apparently age-related neurological deficits resembling Alzheimer’s and has been linked to this disease and to the Guamanian variant, ALS-PDC. Similar outcomes have been found in animal models. In addition, injection of aluminum adjuvants in an attempt to model Gulf War syndrome and associated neurological deficits leads to an ALS phenotype in young male mice. In young children, a highly significant correlation exists between the number of pediatric aluminum-adjuvanted vaccines administered and the rate of autism spectrum disorders. Many of the features of aluminum-induced neurotoxicity may arise, in part, from autoimmune reactions, as part of the ASIA syndrome.

    https://www.ncbi.nlm.nih.gov/pubmed/23609067

    Human Papilloma Virus Vaccine and Primary Ovarian Failure:
    Another Facet of the Autoimmune/Inflammatory Syndrome
    Induced by Adjuvants
    http://www.luontaisnetti.fi/hpv/3%20cases%20of%20Primary%20Ovarian%20Failure%20following%20HPVvaccination,%20Am%20J%20Reproductive%20Immunol%202013.pdf
    https://www.ncbi.nlm.nih.gov/pubmed/23902317

  • Aluminum adjuvants have never required any safety testing.

    Aluminum has been exempted from testing for safety by the FDA under a convoluted logic wherein it is classified as GRAS. (Generally Regarded As Safe.) It has never been tested by the FDA on its safety and there are NO restrictions whatever on the amount or use of aluminum. Diseases Associated with Aluminium Intoxication. H. Tomlinson, M.B., Ch.B., MRCS., LRCP. Since that time thousands of studies have been published indicating aluminum is involved in neurological dysfunction, immunocompetence, as well as a host of other morbidities

    http://www.raysahelian.com/aluminum.html

    Despite the number of references to aluminum toxicity, the FDA has always exempted it from testing from testing by putting it on their “Generally Regarded as Safe” ( GRAS ) list. Aluminum can be added to foods, medicines or water without restriction from the FDA.

    [ Aluminum is known to stop cell division during the “S Phase”, at levels less than 4 ppm. ]

    The mechanism of action of aluminum toxicity is aluminum’s effect on carrying capacity or Zeta Potential. Aluminum is relatively non-toxic in and of itself. However, it destroys the carrying capacity of a liquid.

    Aluminum has three ( 3 ) positive ions, so a single ion of aluminum will reduce surface charge, reduce carrying capacity and increase surface tension by 6,000 times the amount that an ion of Sodium, which has one ( 1 ) positive charge, would.

    Read more:
    http://customers.hbci.com/~wenonah/info/colloid.htm#Altox

    Understanding Colloidal Suspensions

    Colloids are held in suspension via, a very slight Electro-negative charge on the surface of each particle. This charge is called Zeta Potential.

    Zeta Potential = Very slight Electro-negative charge on the “surface” ( Outer Orbital Regions or “Virtual Shell” ) of “particles”. Like charges repel each other, so “Particle Domains” with negative outer regions will move away from each other — Nature’s anti-collision system. { Can you say, “Rubber Baby Buggy Bumper”? } — { Faster } —Tommy—

    The ability of a liquid to carry material in suspension is a function of these minute electrical charges. As the Electro-negative charge increases, more material can be carried in suspension. As the charge decreases, the particles move closer to each other and the liquid is able to carry less material. There is a point where the ability to carry material in suspension is exceeded, and particles begin to clump together with the heavier particles materials dropping out of the liquid and coagulating.

    Read more:
    http://customers.hbci.com/~wenonah/info/colloid.htm

    Zeta Potential

    http://en.wikipedia.org/wiki/Zeta_potential

    Using “Zeta Potential” as a Healing Tool

    http://customers.hbci.com/~wenonah/new/mcdaniel.htm

    — You Must Avoid Aluminum —

    In Your Water, Your Food, and in things you put “In” and “On” Your Body !

    Aluminum is used to treat waste water. It is added to waste water to cause materials to come out of solution and settle to the bottom of the tank.

    The same thing can happen inside your body. 3–4 parts per million* of Aluminum in our blood Will Cause materials to come out of the blood plasma solution forming plaque on blood vessel walls. It also causes blood cells to clump together, thereby blocking blood flow to organs — causing strokes, heart attacks and other problems!

    [ * About 27 milligrams of elemental aluminum in our body’s 7 liters of blood will cause coagulation. ]

    The reason this happens, is because Aluminum has a strong effect on Zeta Potential.

    Aluminum is used in many Vaccinations as a stabilizer, and is known to cause learning disabilities. It can also STOP CELL DIVISION during the “S Phase”.

    Aluminum is Especially Harmful to Children! (And they are injecting multiple vaccines with aluminum adjuvants).

    4 ppm of aluminum in human blood can cause it to colagulate.

    Aluminum in humans is documented to inhibit learning.

    http://customers.hbci.com/~wenonah/new/mcdaniel.htm

    Rivers of Life and Death Part 4
    Vitamin C and Vascular Disease

    Lead increases the toxicity of mercury by a hundred fold, so does aluminum.

    The vasculopathic process Dr. Moulden has named the “MASS response” and this is a type of hypersensitivity response largely mediated by a cell mediated immune response (type 4 hypersensitivity) and this response is active alone, or in combination with the other hypersensitivity responses. According to Moulden vaccine injured cases develop cranial nerve ischemic lesions within hours of vaccine with some dying in the process, others neurocognitively impaired for life, and others develope autism if the damage happens early in life.

    Read more:
    http://www.natmedtalk.com/showthread.php?t=3729

    Dr. Andrew Moulden: Learning to Identify Vaccine Damage
    https://healthimpactnews.com/2015/dr-andrew-moulden-learning-to-identify-vaccine-damage/

  • Karl Wegner MD

    Without controls you don’t even know if they measured the aluminum content correctly or how their results compare to non-autistic brains. Given the variances they found in the same specimens it looks like they didn’t.

  • You can read the study and listen to the explanations that Exley gave, and to easily determine that your in denial and false accusations are entirely baseless. But again then obviously you didn’t even take the time to do that, now did you. And they already know what a normal autopsied brain contains for aluminum, little to none.

  • Karl Wegner MD

    So what explanation did Exley give as to the lack of controls Lowell? (you won’t answer the question)

  • dporter

    What kind of controls & what amount of proving truth would you need to admit the truth of this? You see, we need controls to prove to us that your kneejerk comments aren’t simply due to the connected paycheck, the arrogance of an elite who believes the rest of us need culled or to be made controllable to serve the whims of a steering occulted elite, or perhaps, & in hope of some shred of decency still connected to truth, denial due to unintentional harm done that closes your eyes?

  • Karl Wegner MD

    Bloody peasant.

  • First of all and as I said they of course already know what the aluminum content is within a normal brain. Are you so ignorant that you think that has not been studied at the same time?

    Go ahead and as well now answer dporter’s question to you, (question below)

    [What kind of controls & what amount of proving truth would you need to admit the truth of this?]

    Here we have below, the main high lights of the study. No ware you going to tell me that it would be common for the average atypical person with no significant health issues, to walking around with those high levels of aluminum within their brain? Those high levels and particularly in the areas of the brain, that they were found? You are somehow telling me that this would be considered as common, and normal? You are still telling me that Exley and his co-authors are not aware of what is normal?

    This study follows precisely what other studies have found, high levels of aluminum in the brains of those with autism. Do you really think that they acquired all that aluminum from eating cake or brownies with aluminum containing baking powder in them?

    Dr Russell Blaylock retired neurosurgeon stated that this was happening, already years ago. Studies have as well been done that show aluminum adjuvants to cause over-activation of the brains microglia cells, (largely a part of the brains own reactive immune system), and with resulting chronic levels of brain inflammation. Are you telling me that you still can’t put this together?

    Aluminium in brain tissue in autism
    Matthew Mold, Dorcas Umar, Andrew King, Christopher Exley

    1. Introduction
    Autism spectrum disorder (ASD) is a group of neurodevelopmental conditions of unknown cause. It is highly likely that both genetic [1] and environmental [2] factors are associated with the onset and progress of ASD while the mechanisms underlying its aetiology are expected to be multifactorial [3-6]. Human exposure to aluminium has been implicated in ASD with conclusions being equivocal [7-10]. To-date the majority of studies have used hair as their indicator of human exposure to aluminium while aluminium in blood and urine have also been used to a much more limited extent. Paediatric vaccines that include an aluminium adjuvant are an indirect measure of infant exposure to aluminium and their burgeoning use has been directly correlated with increasing prevalence of ASD [11]. Animal models of ASD continue to support a connection with aluminium and to aluminium adjuvants used in human vaccinations in particular [12]. Hitherto there are no previous reports of aluminium in brain tissue from donors who died with a diagnosis of ASD. We have measured aluminium in brain tissue in autism and identified the location of aluminium in these tissues.

    Page 2

    ABSTRACT

    Autism spectrum disorder is a neurodevelopmental disorder of unknown aetiology. It is suggested to involve both genetic susceptibility and environmental factors including in the latter environmental toxins. Human exposure to the environmental toxin aluminium has been linked, if tentatively, to autism spectrum disorder. Herein we have used transversely heated graphite furnace atomic absorption spectrometry to measure, for the first time, the aluminium content of brain tissue from donors with a diagnosis of autism. We have also used an aluminium-selective fluor to identify aluminium in brain tissue using fluorescence microscopy. The aluminium content of brain tissue in autism was consistently high. The mean (standard deviation) aluminium content across all 5 individuals for each lobe were 3.82(5.42), 2.30(2.00), 2.79(4.05) and 3.82(5.17) g/g dry wt. for the occipital, frontal, temporal and parietal lobes respectively. These are some of the highest values for aluminium in human brain tissue yet recorded and one has to question why, for example, the aluminium content of the occipital lobe of a 15 year old boy would be 8.74 (11.59) g/g dry wt.?

    Aluminium-selective fluorescence microscopy was used to identify aluminium in brain tissue in 10 donors. While aluminium was imaged associated with neurones it appeared to be present intracellularly in microglia-like cells and other inflammatory non-neuronal cells in the meninges, vasculature, grey and white matter. The pre-eminence of intracellular aluminium associated with non-neuronal cells was a standout observation in autism brain tissue and may offer clues as to both the origin of the brain aluminium as well as a putative role in autism spectrum disorder

    Pages 6 and 7.

    3.2. Aluminium fluorescence in brain tissues

    We examined serial brain sections from 10 individuals (3 females and 7 males) who died with a diagnosis of ASD and recorded the presence of aluminium in these tissues (Table S1). Excitation of the complex of aluminium and lumogallion emits characteristic orange fluorescence that appears increasingly bright yellow at higher fluorescence intensities. Aluminium, identified as lumogallion-reactive deposits, was recorded in at least one tissue in all 10 individuals. Autofluorescence of immediately adjacent serial sections confirmed lumogallion fluorescence as indicative of aluminium. Deposits of aluminium were significantly more prevalent in males (129 in 7 individuals) than females (21 in 3 individuals).

    Aluminium-loaded mononuclear white blood cells, probably lymphocytes, were identified in the meninges and possibly in the process of entering brain tissue from the lymphatic system (Fig.1). Aluminium could be clearly seen inside cells as either discrete punctate deposits or as bright yellow fluorescence. Aluminium was located in inflammatory cells associated with the vasculature (Fig. 2). In one case what looks like an aluminium-loaded lymphocyte or monocyte was noted within a blood vessel lumen surrounded by red blood cells while another probable lymphocyte showing intense yellow fluorescence was noted in the adventitia (Fig. 2b). Glial cells including microglia-like cells that showed positive aluminium fluorescence were often observed in brain tissue in the vicinity of aluminium-stained extracellular deposits (Figs. 3&4). Discrete deposits of aluminium approximately 1m in diameter were clearly visible in both round and amoeboid glial cell bodies (e.g. Fig. 3b). Intracellular aluminium was identified in likely neurones and glia-like cells and often in the vicinity of or colocalised with lipofuscin (Fig. 5). Aluminium-selective fluorescence microscopy was successful in identifying aluminium in extracellular and intracellular locations in neurones and non-neuronal cells and across all brain tissues studied (Figs.1-5). The method only identifies aluminium as evidenced by large areas of brain tissue without any characteristic aluminium-positive fluorescence (Fig. S1).

    Page 8.

    4. Discussion

    The aluminium content of brain tissues from donors with a diagnosis of ASD was extremely high (Table 1). While there was significant inter-tissue, inter-lobe and inter-subject variability the mean aluminium content for each lobe across all 5 individuals was towards the higher end of all previous (historical) measurements of brain aluminium content, including iatrogenic disorders such as dialysis encephalopathy [13,15, 16-19]. All 4 male donors had significantly higher concentrations of brain aluminium than the single female donor. We recorded some of the highest values for brain aluminium content ever measured in healthy or diseased tissues in these male ASD donors including values of 17.10, 18.57 and 22.11 g/g dry wt. (Table 1). What discriminates these data from other analyses of brain aluminium in other diseases is the age of the ASD donors. Why, for example would a 15 year old boy have such a high content of aluminium in their brain tissues? There are no comparative data in the scientific literature, the closest being similarly high data for a 42 year old male with familial Alzheimer’s disease (fAD) [19].

    Aluminium-selective fluorescence microscopy has provided indications as to the location of aluminium in these ASD brain tissues (Figs. 1-5). Aluminium was found in both white and grey matter and in both extra- and intracellular locations. The latter were particularly preeminent in these ASD tissues. Cells that morphologically appeared non-neuronal and heavily loaded with aluminium were identified associated with the meninges (Fig. 1), the vasculature (Fig. 2) and within grey and white matter (Figs. 3-5). Some of these cells appeared to be glial (probably astrocytic) whilst others had elongated nuclei giving the appearance of microglia [5]. The latter were sometimes seen in the environment of extracellular aluminium deposition. This implies that aluminium somehow had crossed the blood-brain barrier and was taken up by a native cell namely the microglial cell. Interestingly, the presence of occasional aluminium-laden inflammatory cells in the vasculature and the leptomeninges opens the possibility of a separate mode of entry of aluminium into the brain i.e. intracellularly. However, to allow this second scenario to be of significance one would expect some type of intracerebral insult to occur to allow egress of lymphocytes and monocytes from the vasculature. The identification herein of non-neuronal cells including inflammatory cells, glial cells and microglia loaded with aluminium is a standout observation for ASD. For example, the majority of aluminium deposits identified in brain tissue in fAD were extracellular and nearly always associated with grey matter [19]. Aluminium is cytotoxic [21] and its association herein with inflammatory cells in the vasculature, meninges and central nervous system is unlikely to be benign. Microglia heavily loaded with aluminium while potentially remaining viable, at least for some time, will inevitably be compromised and dysfunctional microglia are thought to be involved in the aetiology of ASD [22], for example in disrupting synaptic pruning [23].

    5. Conclusions
    We have made the first measurements of aluminium in brain tissue in ASD and we have shown that the brain aluminium content is extraordinarily high. We have identified aluminium in brain tissue as both extracellular and intracellular with the latter involving both neurones and non-neuronal cells. The presence of aluminium in inflammatory cells in the meninges, vasculature, grey and white matter is a standout observation and could implicate aluminium in the aetiology of ASD.

    Read more:

    Aluminium in brain tissue in autism
    https://www.sciencedirect.com/science/article/pii/S0946672X17308763
    https://ac.els-cdn.com/S0946672X17308763/1-s2.0-S0946672X17308763-main.pdf?_tid=a4e13100-dae3-11e7-b622-00000aab0f27&acdnat=1512605871_d60dde7ed0388cc4559b3c4efbf91bc7

    Study: Record Levels of Aluminum Found in Autistic Children Brain Tissue

    November 28, 2017 4:04 pm

    11-27-Aluminum_Featured_Image-300×156
    Dr. Christopher Exley—one of the world’s leading experts on aluminum toxicity—has shown that chronic intoxication with myriad forms of this “ubiquitous and omnipresent metal” is exacting a high price on human health. Dr. Exley and other aluminum experts such as molecular biologist Dr. Lucija Tomljenovic have confirmed that aluminum readily and actively traverses the blood-brain barrier to selectively accumulate in brain tissues, where it induces unwelcome changes in brain biochemistry. As Dr. Exley has noted, “There are no ‘normal’ levels of brain aluminum,” meaning that “its presence in brain tissue, at any level, could be construed as abnormal” In light of the fact that even minute amounts of aluminum can have adverse neurological consequences, Dr. Exley’s newest paper—which reports on the first-ever study of aluminum in ASD brain tissue—is groundbreaking. Published in the Journal of Trace Elements in Medicine and Biology, the paper documents some of the highest values for aluminum in human brain tissue ever recorded. Using a two-pronged study design, the researchers measured and characterized aluminum deposits in brain tissues from five to ten ASD donors, most of whom died in their teens or twenties. What the research team found was startling. The study’s quantitative arm documented “consistently high” aluminum levels representing “some of the highest values for brain aluminum content ever measured in healthy or diseased tissues.”

    Read More…
    http://vaccineimpact.com/2017/study-record-levels-of-aluminum-found-in-autistic-children-brain-tissue/

  • Answer the stated question.

  • Karl Wegner MD

    What kind of controls? Gee, maybe brain samples from non-autistic people? It isn’t rocket science.

  • Again, in the video describing what the Exley study team found, he clearly states that the comparison was as well made to the 100 human brains that they have previously studied. If those 100 brains had all been from people with autism, they would have conducted the study long ago.

    Des doses importantes d’aluminium retrouvées dans des cerveaux d’autistes (Pr Chris Exley)
    https://www.youtube.com/watch?time_continue=6&v=SmkVv8pcVhc

    You as well failed to answer any of my questions and which I put to you above. Why is that?

    You are all about the science, but refuse the real study science.

    BRAIN’S IMMUNE SYSTEM TRIGGERED IN AUTISM
    http://www.hopkinsmedicine.org/Press_releases/2004/11_15a_04.html

    Ann Neurol. 2005 Jan;57(1):67-81. Neuroglial activation and neuroinflammation in the brain of patients with autism. Vargas DL, Nascimbene C, Krishnan C, Zimmerman AW, Pardo CA.
    Source: Department of Neurology, Johns Hopkins University School of Medicine, 600 North Wolfe Street, Baltimore, MD 21287, USA.

    Abstract
    Autism is a neurodevelopmental disorder characterized by impaired communication and social interaction and may be accompanied by mental retardation and epilepsy. Its cause remains unknown, despite evidence that genetic, environmental, and immunological factors may play a role in its pathogenesis. To investigate whether immune-mediated mechanisms are involved in the pathogenesis of autism, we used immunocytochemistry, cytokine protein arrays, and enzyme-linked immunosorbent assays to study brain tissues and cerebrospinal fluid (CSF) from autistic patients and determined the magnitude of neuroglial and inflammatory reactions and their cytokine expression profiles. Brain tissues from cerebellum, midfrontal, and cingulate gyrus obtained at autopsy from 11 patients with autism were used for morphological studies. Fresh-frozen tissues available from seven patients and CSF from six living autistic patients were used for cytokine protein profiling. We demonstrate an active neuroinflammatory process in the cerebral cortex, white matter, and notably in cerebellum of autistic patients. Immunocytochemical studies showed marked activation of microglia and astroglia, and cytokine profiling indicated that macrophage chemoattractant protein (MCP)-1 and tumor growth factor-beta1, derived from neuroglia, were the most prevalent cytokines in brain tissues. CSF showed a unique proinflammatory profile of cytokines, including a marked increase in MCP-1. Our findings indicate that innate neuroimmune reactions play a pathogenic role in an undefined proportion of autistic patients, suggesting that future therapies might involve modifying neuroglial responses in the brain.

    http://www.neuro.jhmi.edu/neuroimmunopath/pdf/4%20Neuroglial%20activation%20and%20neuroinflammation%20in%20the%20brain%20of%20patients%20with%20autism.pdf

    http://www.ncbi.nlm.nih.gov/pubmed/15546155

    January 2013
    Microglial Activation in Young Adults With Autism Spectrum Disorder

    Katsuaki Suzuki, MD, PhD; Genichi Sugihara, MD, PhD; Yasuomi Ouchi, MD, PhD; Kazuhiko Nakamura, MD, PhD;
    Masami Futatsubashi, BS; Kiyokazu Takebayashi, MD, PhD; Yujiro Yoshihara, MD, PhD; Kei Omata, PhD;
    Kaori Matsumoto, MA; Kenji J. Tsuchiya, MD, PhD; Yasuhide Iwata, MD, PhD; Masatsugu Tsujii, MA;
    Toshirou Sugiyama, MD, PhD; Norio Mori, MD, PhD

    Context: A growing body of evidence suggests that aberrant immunologic systems underlie the pathophysiologic characteristics of autism spectrum disorder (ASD). However, to our knowledge, no information is available on the patterns of distribution of microglial activation in the brain in ASD.

    Conclusions: Our results indicate excessive microglial activation in multiple brain regions in young adult subjects with ASD. The similar distribution pattern of regional microglial activity in the ASD and control groups may indicate augmented but not altered microglial activation in the brain in the subjects with ASD.

    In conclusion, the present PET measurements revealed marked activation of microglia in multiple brain regions of young adults with ASD. The results strongly support the contention that immune abnormalities contribute to the etiology of ASD. The similar patterns of distribution of regionally activated microglia in these ASD and control groups may indicate the augmented but not altered microglial activation in the brain in the ASD subjects.

    https://vaccinepapers.org/wp-content/uploads/Microglial-activation-in-young-adults-with-autism-spectrum-disorder-1.pdf

    Dr. Paul Offit’s Aluminum Deceptions and Academic Misconduct (one very important article, to read)
    http://vaccinepapers.org/dr-paul-offits-aluminum-deceptions-academic-misconduct/

    Vaccine Papers
    An Objective Look at Vaccine Dangers
    https://vaccinepapers.org/

    A Mechanism of Toxicity of Aluminium-based Adjuvants?
    Consumer Summary | by Chris Exley
    http://www.vaccinesafetyconference.com/exley

    Aluminum as a Neurotoxin: The Evidence from Cell Culture, In Vivo, & Human Studies
    http://www.vaccinesafetyconference.com/pdf/Shaw/Shaw_PPT.pdf

    Aluminum Induced Immunoexcitotoxicity in Neurodevelopmental and Neurodegenerative Disorders
    Russell L. Blaylock*
    Visiting Professor Biology Belhaven University Theoretical Neurosciences Research, LLC Ridgeland, Mississippi, USA

    Abstract

    A great deal has been learned about the neurotoxicity of aluminum over the past two decades in terms of its ability to disrupt cellular function. Newer evidence suggests that a more central pathophysiological mechanism may be responsible for much of the toxicity of aluminum and aluminofluoride compounds on the brain. This mechanism involves activation of the brainâ € ™ s innate immune system, primarily the microglia, with a release of neurotoxic concentrations of excitotoxins and pro-inflammatory cytokines, chemokines and immune mediators. A large number of studies suggest that excitotoxicity plays a significant role in the neurotoxic action of a number of metals, including aluminum. Recently, researchers have found that while most of the chronic neurodegenerative effects of these metals are secondary to prolonged inflammation, it is the enhancement of excitotoxicity by the immune mediators that is responsible for most of the metalâ € ™ s toxicity. This enhancement occurs via a crosstalk between cytokine receptors and glutamate receptors. The author coined the name immunoexcitotoxicity to describe this process. This paper reviews the evidence linking immunoexcitotoxicity to aluminums neurotoxic effects.

    http://www.geoengineeringwatch.org/documents/Aluminum-Blaylock.pdf

    Autism Spectrum Disorders and Aluminum Vaccine Adjuvants
    Lucija Tomljenovic, Russell L. Blaylock, Christopher A. Shaw

    Abstract
    Impaired brain function, excessive inflammation, and autoimmune manifestations are common in autism. Aluminum (Al), the most commonly used vaccine adjuvant, is a demonstrated neurotoxin and a strong immune stimulator. Hence, adjuvant Al has the necessary properties to induce neuroimmune disorders. Because peripheral immune stimuli in the postnatal period can compromise brain development and cause permanent neurological impairments, the possibility that such outcomes could also occur with administration of Al vaccine adjuvants needs to be considered. In regard to the risk of adjuvant toxicity in children, the following should be noted: (i) children should not be viewed as “small adults” as their unique physiology makes them more vulnerable to toxic insults; (ii) in adult humans Al adjuvants can cause a variety of serious autoimmune and inflammatory conditions including those affecting the brain, yet children are routinely exposed to much higher amounts of Al from vaccines than adults; (iii) compelling evidence has underscored the tight connection between the development of the immune system and that of the brain. Thus, it appears plausible that disruptions of critical events in immune development may also play a role in the establishment of neurobehavioral disorders; (iv) the same immune system components that play key roles in brain development appear to be targeted for impairment by Al adjuvants. In summary, research data suggests that vaccines containing Al may be a contributing etiological factor in the increasing incidence of autism.

    http://link.springer.com/referenceworkentry/10.1007%2F978-1-4614-4788-7_89

    Review Article
    Aluminum-Induced Entropy in Biological Systems:
    Implications for Neurological Disease
    http://people.csail.mit.edu/seneff/Shaw_et_al_JOT_2014.pdf

    J Inorg Biochem. 2013 No;128:237-44. doi: 10.1016/j.jinorgbio.2013.07.022. Epub 2013 Jul 19.
    Administration of aluminium to neonatal mice in vaccine-relevant amounts is associated with adverse long term neurological outcomes.
    http://www.ncbi.nlm.nih.gov/pubmed/23932735

    Journal of American Nutraceutical Association 6: 21-35, 2003.
    Interaction of Cytokines, Excitotoxins, and Reactive Nitrogen and Oxygen Species in Autism Spectrum Disorders, Russell Blaylock, MD* Medical Director, Advanced Nutritional Concepts Ridgeland, Mississippi
    http://www.nutrimedical.com/news.jhtml?method=view&news.id=1084

    Session 22, The Vaccine Safety Conference: Dr. Russell Blaylock, MD, CCN
    THE CENTRAL ROLE OF IMMUNOEXCITOTOXICITY IN ALUMINUM AND MERCURY-CONTAINING ADJUVANT-TRIGGERED NEURODEVELOPMENTAL AND NEURODEGENERATIVE DISORDERS
    http://www.youtube.com/watch?v=u9DkcpEEBPI

    Clinical Features of Gulf War Syndrome and Autism
    Russell L. Blaylock, M.D.

    ABSTRACT
    There is considerable and growing evidence that chronic microglial activation plays a major role in numerous neurological conditions including Alzheimer’s dementia, Parkinson’s disease,ALS, strokes, and inflammatory brain diseases. The release of toxic elements from activated microglia, such as cytokines and excitotoxins, is known to produce neurodegeneration. Peripheral immune stimulation has been shown to activate CNS microglia, and when excessive can lead to neurodegeneration and cognitive defects commonly associated with both the Gulf War Syndrome (GWS) and autism. This paper summarizes the mechanism linking these two disorders with excessive immune stimulation secondary to overvaccination.

    http://www.jpands.org/vol9no2/blaylock.pd

    How Vaccines Harm Child Brain Development – Dr Russell Blaylock MD
    http://www.youtube.com/watch?v=7QBcMYqlaDs

    Vaccines adversely effect the brain health of adults as well.

    Vaccines, Depression and Neurodegeneration After Age 50 Years
    https://heartmdinstitute.com/health-and-wellness/vaccines-depression-neurodegeneration-after-age-50-years/?showall=

    The Danger of Excessive Vaccination During Brain Development, by Dr Russell Blaylock
    http://articles.mercola.com/sites/articles/archive/2008/03/14/the-danger-of-excessive-vaccination-during-brain-development.aspx

    Entropy 2012, 14(8), 1399-1442; doi:10.3390/e14081399
    Review
    The Initial Common Pathway of Inflammation, Disease, and Sudden Death
    Robert M. Davidson 1,* and Stephanie Seneff
    http://www.mdpi.com/1099-4300/14/8/1399
    http://people.csail.mit.edu/seneff/Entropy/Entropy1_downloaded.pdf

    Warning to Pregnant Mothers – Toxic Dose of Aluminum in the Tdap
    https://www.youtube.com/watch?v=VoY6vXEMsU8

    Warning to Pregnant Mothers- Toxic Dose of Aluminum in the Tdap
    http://paulthomasmd.com/2012/12/11/warning-to-pregnant-mothers-toxic-dose-of-aluminum-in-the-tdap/

    Aluminum in Vaccines | A Pediatricians Warning To All Parents
    https://www.youtube.com/watch?v=ee70I5bm3-k

    Slow CCL2-dependent translocation of biopersistent particles from muscle to brain

    Conclusion

    Nanomaterials can be transported by monocyte-lineage cells to DLNs, blood and spleen, and, similarly to HIV, may use CCL2-dependent mechanisms to penetrate the brain. This occurs at a very low rate in normal conditions explaining good overall tolerance of alum despite its strong neurotoxic potential. However, continuously escalating doses of this poorly biodegradable adjuvant in the population may become insidiously unsafe, especially in the case of overimmunization or immature/altered blood brain barrier or high constitutive CCL-2 production.

    http://www.ncbi.nlm.nih.gov/pubmed/23557144
    http://www.biomedcentral.com/1741-7015/11/99

    Microglia in the developing brain: A potential target with lifetime effects

    National Toxicology Program Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, NC, USA

    http://www.sciencedirect.com/science/article/pii/S0161813X12000277

    Cell Biology and Toxicology
    April 2013, Volume 29, Issue 2, pp 75-84
    How aluminum, an intracellular ROS generator promotes hepatic and neurological diseases: the metabolic tale
    http://link.springer.com/article/10.1007%2Fs10565-013-9239-0

    Mechanisms of aluminum adjuvant toxicity and autoimmunity in pediatric populations http://lup.sagepub.com/content/21/2/223.short http://www.ncbi.nlm.nih.gov/pubmed/22235057

    Autoimmune or auto-inflammatory syndrome induced by adjuvants (ASIA):
    Old truths and a new syndrome?
    Pier Luigi Meroni a,b,*
    http://xa.yimg.com/kq/groups/16063327/1870391070/name/ASIA3.pdf

    Self-Organized Criticality Theory of Autoimmunity

    Conclusions/Significance

    Systemic autoimmunity appears to be the inevitable consequence of over-stimulating the host’s immune ‘system’ by repeated immunization with antigen, to the levels that surpass system’s self-organized criticality.

    http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0008382 (Full study)

    Vaccines and Brain Inflammation, Harold Buttram, MD , and Catherine Frompovich
    http://www.vaccinationcouncil.org/2011/06/01/vaccines-and-brain-inflammation/

    A Parent’s Primer: Vasculitis and Vaccines, (more inflammation problems, likely due to the aluminum adjuvants, this time its in the blood vessels)
    http://sanevax.org/a-parents-primer-vasculitis-and-vaccines/

    How the aluminum adjuvants cause this said inflammation.

    J Immunol. 2008 Sep 15;181(6):3755-9. Cutting edge: alum adjuvant stimulates inflammatory dendritic cells through activation of the NALP3 inflammasome.
    http://www.ncbi.nlm.nih.gov/pubmed/18768827

    Hypothesis Neuro-inflammation, blood-brain barrier, seizures and autism http://www.jneuroinflammation.com/content/8/1/168

    Research The NALP3 inflammasome is involved in neurotoxic prion peptide-induced microglial activation http://www.jneuroinflammation.com/content/9/1/73/abstract

  • Karl Wegner MD

    Back to gish galloping. Without controls you have no idea if their measurements were accurate. It’s basically a quality control thing. That whooshing sound is this concept going over your bald head.

  • You can end the lying and in denial pro-vax shillary charade now. Everyone can now see directly what all has and continues to go over YOUR head. If you can not put it all together that clearly Exley’s study is correct, and with the study science and the data that I have now put in front of you; then you obviously need to have the hole in your head fixed.

  • Karl Wegner MD

    You have no idea if Exley is correct.

  • I just proved without any reasonable doubt that Exley is right. Come on you claimed purveyor of the science, dig into those studies and actually educate yourself. Your level of denial will not let you. You must continue to present with nothing but complete pro-vax denial, and no matter what.

  • Karl Wegner MD

    Nothing you copy/pasted helps his non-controlled study look better.

  • You know you yourself look like $hit right now, and that it couldn’t possible even look any worse for your pathetic arse. So take your delusions and go live your sick fantasy somewhere else.

    When have you ever scientifically studied 100 donated brains, and 10 comparatively with diagnosed autism? How much experience do you have in using the described diagnostic equipment that Exley used? The answer is obviously, none.

  • Karl Wegner MD

    None of that matters.

  • Karl Wegner MD

    What Exley claims to have done in the past has nothing to do with the lack of controls in this study. It was just another anti-vax waste of resources.

  • The controls were the 100 brains that were donated and studied previously. What do you not get about that the average neuro-typical individual walking around, does not have high levels of aluminum existing within their brain, and as well not in the areas of the brain that the aluminum was found? What do you not get about that physiologically based conclusion? The 10 brains that were donated to science and which came from individuals with autism, were no old people; they were relatively young people. Again, where do you think that aluminum came from; the aluminum content within the baking powder contained in the cake and brownies they ate for a snack?

    Polysorbate 80 is as well an ingredient in vaccines. Polysorbate 80 is clearly known to open the blood brain barrier and make it more permeable, thus allowing substances like aluminum to much more easily cross the blood/brain barrier. Why is an ingredient in vaccines at all that makes the blood/brain barrier more permeable? Then when you consider the long list of ingredients in injected vaccines, adding polysorbate 80 is unconscionable. If the dose of polysorbate 80 is high enough it has as well been shown to cause excessive growth in and early reproductive maturity, and with resulting infertility in young rats.

    All of the studies that I put forth as well here, put this all together perfectly; but you obviously as well did not even take the time to honestly review any of that.

    Actually review the data and studies I posted here that have previously found chronic levels of brain inflammation in children and individuals with autism. Johns Hopkins did and was just one of the study sources for that information. Then you go to the existing studies that show adjuvant aluminum directly causes over-activation of the brains microglia cells, and with resulting chronic levels of brain inflammation. When you put that all together, the right and proper conclusions becomes clearly evident, and which is something that you have obviously no intellectual capability in doing.

  • Nothing would ever be enough to allow and to get you to admit to the obvious truth. You have continually made denial of everything and no matter how strong the evidence is. Nothing would ever be enough for you, and that is all to obvious. You must deny the major significance of it all, and no matter what.

  • Indeed it does matter. It matters as well in regard to the health and the lives of millions of children, and their families. All you care about is remaining in denial. All you care about is maintaining the re-parroted safe and effective known false vaccine propaganda. All you care about and in hate filled teeth-gnashing form, is repeatedly attempting to protect the careers within the Pediatrics field; and that while making complete denial as well of all the obvious harm they have done to child health, directly by the means of toxic and contaminated repeat vaccination.

  • Karl Wegner MD

    If you have evidence 100 other brains were previously evaluated for aluminum levels using the exact same techniques (transversely heated graphite furnace atomic absorption spectrometry and aluminium-selective fluorescence microscopy) let’s see it. (you don’t have it). They didn’t use any controls you dolt.

  • Karl Wegner MD

    For studies like this controls (and even better replication of the results by others) would be required. The nonsense you spam doesn’t cut it though, that much is true.

  • Karl Wegner MD

    What matters is people potentially stopping children’s vaccinations because of more anti-vax pseudoscience.

  • You can easily see the the study science I have put in front of you is very real and not pseudoscience.

    This is an example directly of real pseudoscience. And then in their quackery filled minds, they say the science is settled and with there being no further need of any additional vaccine safety studies. The pro-vax sound more like they really don’t want to know what is going on with their vaccines?

    Lets also take a look at the existing studies that allegedly show no connection between vaccines and autism. Actually, general vaccine injury, and immunological harm done, and without the evidence of autism, is an equally as serious an issue.

    As for their known epidemiological studies.

    And, what did they study in those so called and claimed to larger epidemiological, (population based), vaccine safety studies? In fact they only studied one single vaccine, the MMR; and one single vaccine ingredient, Thimerosal. None of the larger epidemiological studies compared vaccinated to entirely unvaccinated. None of the studies looked at the safety profile of the entire CDC vaccine schedule. None of those studies as well looked at the safety profile of giving from 5 to up to 9 vaccines or more to and infant or small child, in a single day and office visit.

    Every one of the larger MMR, and Thimerosal epidemiolgical studies were clearly COOKED, for the results, period. Found were the use of flawed study designs, use of unrealiable data, predetermined outcomes unsupported by the data, and as well major conflicts of interest in the studies funding sources; none of them being independent and nor unbiased.

    VACCINES AND AUTISM – WHAT DO EPIDEMIOLOGICAL STUDIES REALLY TELL US? (This is a well done analysis of all the large studies that they still use as well at the federal vaccine court to deny children’s families compensation for vaccine caused autism)

    We have 16 studies already that clearly state that vaccines do not cause autism.”
    — Amy Pisani, Executive Director, Every Child By Two

    “16 studies have shown no causal association between vaccines and autism, and these
    studies carry weight in the scientific industry.”
    — Dr. Nancy Snyderman, NBC Today Show Medical Editor

    “The science is largely complete. Ten epidemiological studies have shown MMR vaccine
    doesn’t cause autism; six have shown thimerosal doesn’t cause autism.”
    — Dr. Paul Offit, “Autism’s False Prophets”

    Read more:
    http://www.rescuepost.com/files/vaccines-and-autism-epidemiology-rebuttal.pdf

    14 Studies
    http://www.fourteenstudies.org

  • Actually I did a very good job of putting that all together. You can now easily see what the study science is showing us; (but you would actually need to follow and read those studies to accomplish that, and which of course you entirely ignored). In fact it is a very damning picture in regard to the safety of vaccines. You can throw your false dirt and lie about that all you want.

  • They obviously have enough experience with testing that they know that a normal brain does not contain high levels of aluminum. Again, you failed to answer my previous questions on that, directly. I provided you direct and specific questions, and which deserve specific answers. Go back and answer those. Anyone with any honesty and which has followed all of this, can easily see who the “REAL . . . DOLT” is.

  • Karl Wegner MD

    You’re just too uneducated to understand Lowell. You don’t even believe in germ theory.

  • Karl Wegner MD

    Again, despite all the links you spam you can’t make Exley’s study credible.

  • Karl Wegner MD

    Like I said you don’t have it.

  • No, again it is you that doesn’t have it. You are just to hatefully stubborn to ever give it up, and no matter how bad and into complete in denial madness, you are and look.

  • And you continue with, and you still can not reply with anything but lies. Your problem has never been with me, but the people that created this horrid vaccine harm situation. Go after them.

  • Quite obviously what I put forth puts it all directly into easily understood terms. So you deflect again but attempting to move the goal posts. I think that your worthless well known and over-used sill debating handbook has more than long worn out. And you can’t even define what I know and believe regarding the germ theory, and because you don’t even know. So instead you simply attempt to mindlessly stereo-type it and all anti-vax people into one category of thinking.

    Lets see if you can go one up and do any comprehending of what this information is showing us? Go ahead and respond to that and as i know you can’t actually do. I know that-that will be the first time that you have ever actually read any of the references that I have posted, and if you do. And this as well does have to do with that germ theory.

    Profound Implications of the Virome for Human Health and Autoimmunity
    http://www.greenmedinfo.com/blog/profound-implications-virome-human-health-and-autoimmunity

  • Ron Roy

    What matters is people potentially stopping children’s vaccinations because the vaccination pseudoscience has been exposed. FTFY.

  • Karl Wegner MD

    And you still don’t.

  • Karl Wegner MD

    I’m not lying. They didn’t use controls so their study will never be taken seriously.

  • Karl Wegner MD

    You claim Bechamp was right but you don’t even understand his theory. You’re just a mess Lowell.

  • Karl Wegner MD

    That doesn’t make any sense Ronald.

  • I clearly understand the comparative theories between Bechamp and Pasteur, and it is actually and obviously you that is a quackery promoting mess. And you simply moved the goal posts because tou can not actually respond to anything that was previously in front of you. Typical pro-vax shill. None of you have anything original, and none of you ever have any study science. You don’t, and because you know that it would be immediately shot down. You do nothing but follow the same disgusting and sick format of BS that you know other shills have attempted. Nothing is ever original, ever. And really, that gets no where in determination of the vaccine risks, and you do that only to provide for more senseless distraction and disruption. Not a one of you shills have and nor can operate in any other way.

    Actually I think it is you that doesn’t know anything about it.

    Germ Theories (Pasteur verses Becamp)

    Germ Theories

    GERM THEORY (Pasteur)

    Disease arises from micro-organisms outside the body.

    Microorganisms are generally to be guarded against.

    The function of microorganisms is constant.

    The shapes and colours of microorganisms are constant

    Every disease is associated with a partciular microorganism

    Microorganisms are primary causal agents.

    Disease can “strike” anybody.

    To prevent disease we have to “build defences”.

    CELLULAR THEORY (Bechamp)

    1. Disease arises from micro-organisms within the cells of the body.

    2.These intracellular microorganisms normally function to build and assist in the metabolic processes of the body.

    3.The function of these organisms changes to assist in the catabolic (disintegration) processes of the host organism when that organism dies or is injured, which may be chemical as well as mechanical.

    4.Microrganisms change their shapes and colours to reflect the medium

    5. Every disease is associated with a particular condition.

    6. Microorganisms become “pathogenic” as the health of the host organism deteriorates. Hence, the condition of the host organism is the primary causal agent.

    7. Disease is built by unhealthy conditions.

    8. To prevent disease we have to create health.

    http://www.whale.to/p/bechamp.html

    The Blood and its Third Anatomical Element
    http://www.whale.to/v/bechamp_b.html

    Rethinking Pasteur’s Germ Theory: How to Maintain Your Optimal Health [Paperback]
    http://www.amazon.com/Rethinking-Pasteurs-Germ-Theory-Maintain/dp/1583940510/ref=pd_sim_b_1

    Stopping Inflammation: Relieving the Cause of Degenerative Diseases
    http://www.amazon.com/Stopping-Inflammation-Relieving-Degenerative-Diseases/dp/0757001483/ref=pd_sim_b_6

    The following biography of Antoine Bechamp is by Montague R. Leverson, the translator of the 1912 edition of The Blood and its Third Element.
    http://www.metropolisink.com/bechamp/index.htm

  • For that to not make any sense to, you would need to be entirely unaware of and blind to anything that has been published for articles on this website, and as well anything that has been reply posted here. What the CDC has is not only pseudoscience, but a serious lack of any vaccine safety science. They only looked at one single vaccine with epidemiological studies that they paid for and cooked the results. Then they looked at only Thimerosal in the same way; then declaring all the needed science as being in and the science as being settled. And thousands of children and their families have suffered for it. All while they keep their sick careers and with no accountability and no legal liability.

    As for their known epidemiological studies.

    And, what did they study in those so called and claimed to larger epidemiological, (population based), vaccine safety studies? In fact they only studied one single vaccine, the MMR; and one single vaccine ingredient, Thimerosal. None of the larger epidemiological studies compared vaccinated to entirely un-vaccinated. None of the studies looked at the safety profile of the entire CDC vaccine schedule. None of those studies as well looked at the safety profile of giving from 5 to up to 9 vaccines or more to and infant or small child, in a single day and office visit.

    Every one of the larger MMR, and Thimerosal epidemiological studies were clearly COOKED, for the results, period. Found were the use of flawed study designs, use of unreliable data, predetermined outcomes unsupported by the data, and as well major conflicts of interest in the studies funding sources; none of them being independent and nor unbiased.

    VACCINES AND AUTISM – WHAT DO EPIDEMIOLOGICAL STUDIES REALLY TELL US?
    http://www.rescuepost.com/files/vaccines-and-autism-epidemiology-rebuttal.pdf

    14 Studies
    http://www.fourteenstudies.org/

  • You are lying, and because the controls issue as for this study, is irrelevant. The comparative aluminum content in a normal human brain is known to be zero or near to zero. The study we are talking about is the most damning study that has ever been. When you have that study and along with all the other supporting studies that i have given you, the whole understanding of what is actually taking place, comes together perfectly. And yet you can not comprehend that and because within your in denial mind you refuse to.

    Here is some more information that you can put right along side of everything that has been presented to you already. Aluminum adjuvants have never been studied for safety, and they were never required to be studied for safety, as 80 plus years ago when aluminum was used only in foods and other non consumed products, the FDA at the time gave aluminum a status of GRAS, generally regarded as safe. Since that time, the use of aluminum has been essentially unrestricted. Big mistake. And you claim that you have the science and that the science exists, and that I don’t have anything. What an in denial disgusting, liar.

    Always new and added to information.

    New study: Massive Aluminum levels in Autism brains, is this the smoking gun for vaccines?
    https://medium.com/@jbhandley/new-study-massive-aluminum-levels-in-autism-brains-is-this-the-smoking-gun-for-vaccines-54ae85ec2a9c

    Immune Activation & Autism – Aluminum Adjuvant & Immune Activation (this brochure page is packed with direct information on aluminum and adjuvants)
    http://vaccinepapers.org/wp-content/uploads/Autism-brochure-Color-8.5×11.pdf

    Aluminum Toxicity – DETOXIFY – Dr. Christopher Exley- The Systemic Toxicity of Aluminium Adjuvants.

    Dr Christopher Exley. Lecture on the Mechanism of toxicity of aluminum-baced adjuvants. An overview of the accumulation of aluminum in the human body and steps we can take to detoxify. Dr. Christopher Exley is the speaker in Bioinorganic Chemistry at The Birchall Centre, Keele University in Staffordshire and Honorary Professor at the UHI Millennium Institute. Exley is a biologist (University of Stirling) with a PhD in the ecotoxicology of aluminium (University of Stirling). His research career (1984-present) has focused upon an intriguing paradox; ‘how the third most abundant element of the Earth’s crust (aluminium) is non-essential and largely inimical to life’. Investigating this mystery has required research in myriad fields from the basic inorganic chemistry of the reaction of aluminium and silicon to the potentially complex biological availability of aluminium in humans. Exley is 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 area of study forms a large part of Exley’s research.

    https://www.youtube.com/watch?time_continue=3&v=Xleocy6karo

    French scientists sound the alarm about aluminum in vaccines — crickets from media and health authorities
    https://healthcareinamerica.us/french-scientists-sound-the-alarm-about-aluminum-in-vaccines-crickets-from-media-and-health-d3fc0fe23079

    Non-linear dose-response of aluminium hydroxide adjuvant particles: Selective low dose neurotoxicity.
    Crépeaux G, et al. Toxicology. 2017.

    Abstract
    Aluminium (Al) oxyhydroxide (Alhydrogel(®)), the main adjuvant licensed for human and animal vaccines, consists of primary nanoparticles that spontaneously agglomerate. Concerns about its safety emerged following recognition of its unexpectedly long-lasting biopersistence within immune cells in some individuals, and reports of chronic fatigue syndrome, cognitive dysfunction, myalgia, dysautonomia and autoimmune/inflammatory features temporally linked to multiple Al-containing vaccine administrations. Mouse experiments have documented its capture and slow transportation by monocyte-lineage cells from the injected muscle to lymphoid organs and eventually the brain. The present study aimed at evaluating mouse brain function and Al concentration 180days after injection of various doses of Alhydrogel(®) (200, 400 and 800μg Al/kg of body weight) in the tibialis anterior muscle in adult female CD1 mice. Cognitive and motor performances were assessed by 8 validated tests, microglial activation by Iba-1 immunohistochemistry, and Al level by graphite furnace atomic absorption spectroscopy. An unusual neuro-toxicological pattern limited to a low dose of Alhydrogel(®) was observed. Neurobehavioural changes, including decreased activity levels and altered anxiety-like behaviour, were observed compared to controls in animals exposed to 200μg Al/kg but not at 400 and 800μg Al/kg. Consistently, microglial number appeared increased in the ventral forebrain of the 200μg Al/kg group. Cerebral Al levels were selectively increased in animals exposed to the lowest dose, while muscle granulomas had almost completely disappeared at 6 months in these animals. We conclude that Alhydrogel(®) injected at low dose in mouse muscle may selectively induce long-term Al cerebral accumulation and neurotoxic effects. To explain this unexpected result, an avenue that could be explored in the future relates to the adjuvant size since the injected suspensions corresponding to the lowest dose, but not to the highest doses, exclusively contained small agglomerates in the bacteria-size range known to favour capture and, presumably, transportation by monocyte-lineage cells. In any event, the view that Alhydrogel(®) neurotoxicity obeys “the dose makes the poison” rule of classical chemical toxicity appears overly simplistic

  • What you still don’t have, is any aluminum adjuvant safety studies to counter anything that I have put forth here on this article. For how many more weeks of your reply posting here will I have to wait before i see any from you? None exist, and that is directly why you don’t have any. And you just keep on getting your own arse handed to you and each and every time, and yet you come back for more. That is serious level of personal sickness that you have going on, and if you ask me.

  • Karl Wegner MD

    There you go with Whale again. Where are the microzymes Lowell? Oh yeah, you don’t think Bechamp believed in them do you?

  • Karl Wegner MD

    The pseudoscience is anti-vax funded anti-vax scientists still trying to blame vaccines for autism.

  • Karl Wegner MD

    There’s no way to know if they measured the aluminum levels accurately without controls, nor how their results compare to non-autistic brains.

  • Karl Wegner MD

    And you still don’t.

  • Barzini

    Vaccination is child abuse

  • Welcome to the Injecting Aluminum FREE 7 Day Replay event! The full feature film documentary is FREE to watch until December 14 at noon PST.
    Spread the word about Aluminum in vaccines!

    One of several presenters in this video series, “Mr. Aluminum”, Dr. Christopher Exley, biologist at the University of Stirling with a PhD in the Ecotoxicology of Aluminum.

    http://cinemalibrestudio.com/injecting-aluminum/IAevent.html

    Injecting Aluminum | Trailer
    https://vimeo.com/237018558

    Injecting Aluminum
    http://cinemalibrestudio.com/injecting-aluminum/index.html

    Amount of aluminum in vaccines include: (per injected dose)

    Hib (PedVaxHib brand only) – .225 mg per shot
    Hepatitis B – .25 mg
    DTaP – depending on the manufacturer, ranges from .17 to .625 mg
    Pneumococcus – .125 mg
    Hepatitis A – .25 mcg
    HPV – .225 mg
    Pentacel (DTaP, HIB and Polio combo vaccine) – .33 mcg
    Pediarix (DTaP, Hep B and Polio combo vaccine) – .85 mcg

    Christopher Exley is one of the foremost experts on aluminum and aluminum toxicity within the human body. Listen as he explains and describes the results of his recent aluminum adjuvant related vaccine study, with co-authors!!! The title of that study is, Aluminium in brain tissue in autism;
    https://www.youtube.com/watch?time_continue=6&v=SmkVv8pcVhc

    The Toxicity of Aluminum Adjuvants
    Christopher Exley
    https://www.youtube.com/watch?v=zaExaqCv5vo

    Dr. Exley on Vaccines, PhD in Ecotoxicology of Aluminum, University of Stirling
    https://www.youtube.com/watch?v=il6wH81qHAo

    Christopher Exley, more informational videos on aluminum toxicity.
    https://www.youtube.com/results?search_query=Christopher+Exley+aluminum+study+

    Study: Record Levels of Aluminum Found in Autistic Children Brain Tissue

    November 28, 2017 4:04 pm

    11-27-Aluminum_Featured_Image-300×156
    Dr. Christopher Exley—one of the world’s leading experts on aluminum toxicity—has shown that chronic intoxication with myriad forms of this “ubiquitous and omnipresent metal” is exacting a high price on human health. Dr. Exley and other aluminum experts such as molecular biologist Dr. Lucija Tomljenovic have confirmed that aluminum readily and actively traverses the blood-brain barrier to selectively accumulate in brain tissues, where it induces unwelcome changes in brain biochemistry. As Dr. Exley has noted, “There are no ‘normal’ levels of brain aluminum,” meaning that “its presence in brain tissue, at any level, could be construed as abnormal” In light of the fact that even minute amounts of aluminum can have adverse neurological consequences, Dr. Exley’s newest paper—which reports on the first-ever study of aluminum in ASD brain tissue—is groundbreaking. Published in the Journal of Trace Elements in Medicine and Biology, the paper documents some of the highest values for aluminum in human brain tissue ever recorded. Using a two-pronged study design, the researchers measured and characterized aluminum deposits in brain tissues from five to ten ASD donors, most of whom died in their teens or twenties. What the research team found was startling. The study’s quantitative arm documented “consistently high” aluminum levels representing “some of the highest values for brain aluminum content ever measured in healthy or diseased tissues.”

    Read More…
    http://vaccineimpact.com/2017/study-record-levels-of-aluminum-found-in-autistic-children-brain-tissue/

    Aluminium in brain tissue in autism

    Abstract
    Autism spectrum disorder is a neurodevelopmental disorder of unknown aetiology. It is suggested to involve both genetic susceptibility and environmental factors including in the latter environmental toxins. Human exposure to the environmental toxin aluminium has been linked, if tentatively, to autism spectrum disorder. Herein we have used transversely heated graphite furnace atomic absorption spectrometry to measure, for the first time, the aluminium content of brain tissue from donors with a diagnosis of autism. We have also used an aluminium-selective fluor to identify aluminium in brain tissue using fluorescence microscopy. The aluminium content of brain tissue in autism was consistently high. The mean (standard deviation) aluminium content across all 5 individuals for each lobe were 3.82(5.42), 2.30(2.00), 2.79(4.05) and 3.82(5.17) μg/g dry wt. for the occipital, frontal, temporal and parietal lobes respectively. These are some of the highest values for aluminium in human brain tissue yet recorded and one has to question why, for example, the aluminium content of the occipital lobe of a 15 year old boy would be 8.74 (11.59) μg/g dry wt.? Aluminium-selective fluorescence microscopy was used to identify aluminium in brain tissue in 10 donors. While aluminium was imaged associated with neurones it appeared to be present intracellularly in microglia-like cells and other inflammatory non-neuronal cells in the meninges, vasculature, grey and white matter. The pre-eminence of intracellular aluminium associated with non-neuronal cells was a standout observation in autism brain tissue and may offer clues as to both the origin of the brain aluminium as well as a putative role in autism spectrum disorder.

    https://www.sciencedirect.com/science/article/pii/S0946672X17308763

    Full study: (scroll down on page)
    https://ac.els-cdn.com/S0946672X17308763/1-s2.0-S0946672X17308763-main.pdf?_tid=f2be2fde-d56d-11e7-9e32-00000aab0f27&acdnat=1512005566_4d3d686804922e47e0b559810404e854

    New Study: 10x more aluminum in brains with autism

    From our friends at the Children’s Medical Safety Research Institute

    Discovery of “Shockingly High” Levels of Aluminum in Brains of Individuals with Autism Suggests Link with Aluminum-Containing Vaccines

    STAFFORDSHIRE, UNITED KINGDOM–(Marketwired – November 28, 2017) – A new study published in the Journal of Trace Elements in Medicine and Biology provides the strongest indication yet that aluminum is an etiological agent in autism spectrum disorder (ASD), according to researchers at Keele University in England.

    The study used transversely heated graphite furnace atomic absorption spectrometry to measure, for the first time, the aluminum content of brain tissue from five donors who had died with diagnoses of ASD. The results showed the donors to have had some of the highest values of aluminum yet measured in human brain tissue.

    The mean (standard deviation) aluminum content across all five individuals for each lobe were 3.82(5.42), 2.30(2.00), 2.79(4.05) and 3.82(5.17) mg/g dry wt. for the occipital, frontal, temporal and parietal lobes respectively. Previous measurements of 60 brains from humans not diagnosed with ASD showed an average content of 1 mg/g dry wt. of brain tissue.

    “One has to wonder why aluminum in the occipital lobe of a 15-year-old boy with autism would be a value that is at least 10 times higher than what might be considered acceptable for an elderly adult?” said Christopher Exley PhD, Professor in Bioinorganic Chemistry and author of the study. Another ground-breaking study by Exley and his team, published earlier in the year, identified similarly high levels of aluminum in the brains of individuals who died of familial Alzheimer’s disease.

    While the aluminum content of each of the five brains was extraordinarily high, it was the location of the aluminum in the brain tissue that served as the standout observation. The majority of aluminum was identified inside non-neuronal cells including microglia and astrocytes. Aluminum was also found in lymphocytes in the meninges and in similar inflammatory cells in the vasculature. According to the researchers, there was clear evidence of inflammatory cells heavily loaded with aluminum entering the brain via the meningeal membranes and the blood-brain-barrier.

    Aluminum-selective fluorescence microscopy was used to identify aluminum in the brain tissue of 10 donors. The results strongly suggest that aluminum is entering the brain in ASD via pro-inflammatory cells which have become loaded up with aluminum in the blood and/or lymph, much as has been demonstrated for monocytes at injection sites for vaccines including aluminum adjuvants.

    The fact that the majority of aluminum found in brain tissues in ASD was intracellular and associated with non-neuronal cells is, at least for now, unique to ASD and may begin to explain why young adolescents had so much aluminum in their brains.

    “The research does not infer that Al is a cause of autism, “said Exley, who also authored Human Exposure to Aluminum. “But these very high concentrations of a neurotoxin in brain tissue are not going to be benign and will contribute to neurodegeneration in affected tissues.”

    This study was funded by the Children’s Medical Safety Research Institute, a 502(c)3 nonprofit organization dedicated to funding independent research into the causal factors behind today’s epidemic of childhood chronic illness and disability.

    Access to the full article here:
    https://www.sciencedirect.com/science/article/pii/S0946672X17308763

    November 28, 2017 07:00 ET
    Discovery of “Shockingly High” Levels of Aluminum in Brains of Individuals with Autism Suggests Link with Aluminum-Containing Vaccines
    http://www.marketwired.com/press-release/discovery-shockingly-high-levels-aluminum-brains-individuals-with-autism-suggests-link-2241940.htm

    Big Pharma and Big Profits: The Multibillion Dollar Vaccine Market – New Report says “Vaccine Market” Worth $61 Billion by 2020
    https://www.globalresearch.ca/big-pharma-and-big-profits-the-multibillion-dollar-vaccine-market/5503945

  • You still don’t have anything but persistent, denial.

  • The site source is irrelevant; those are known and the exact principals of Becamp and verses Pasteur. Are you denying that?

  • Karl Wegner MD

    And still don’t.

  • Karl Wegner MD

    Where are the microzymes Lowell?

  • AutismDadd

    What an inspiring read and inspiring research. Note is doesn’t come from Big Pharma or CDC.

  • AutismDadd

    More like Crimes against Humanity. Criminal negligence causing harm and death. Criminal Fraud.

  • AutismDadd

    You are a Pharma STOOGE. What would you do with information from those w/o aluminum in their brains? As if you could find any.

  • AutismDadd

    bloody shill

  • AutismDadd

    What about BILLIONS spent on the Genome Project so buttcrack researchers could tell us children with autism have genes?

  • AutismDadd

    Explain the relevance controls would contribute troll

  • AutismDadd

    And you have no class

  • AutismDadd

    Karl you are nothing but a pos troll

  • Karl Wegner MD

    The point is to see whether these researchers would be able to find brains that didn’t have aluminum. Flagged by the way.

  • Karl Wegner MD

    Flagged.

  • Karl Wegner MD

    Educate yourself about the human genome project if that’s possible.

  • Karl Wegner MD

    Would be nice to verify that with the methods used they were able to find different aluminum levels in autistic vs non-autistic brains for starters.

  • Karl Wegner MD

    Flagged.

  • Karl Wegner MD

    Flagged and blocked. Have a nice life.

  • Did I mention microzymes? No, you did. So tell me about them?

  • You hypocritical and whining baby. Grow some balls!!!!

  • AutismDadd

    And that matters how?

  • AutismDadd

    Nice deflection

  • AutismDadd

    snicker

  • AutismDadd

    And then what?

  • Don’t what? So in your mind you are still thinking that atypical people without autism are walking around everywhere and with a large load of aluminum in their brains, and just like Exley found in that study and in the same areas of the brain as this study team found it. You are still thinking that Exley and nor anyone else that has studied human brain science, that no one has ever studied and determined what the normal human being has for aluminum content in their brain. Certainly alzheimers has been extensively studied and they find the same thing, excessive amounts of aluminum in the brain and resulting amyloid plaque which the immune system has created surrounding those areas of the brain which have aluminum contained in them. And yet you claim to think that no scientist anywhere, and to include Exley, has ever determined what a normal aluminum content is and within the normal and atypical human brain. So you maintain that Exley even though they previously examined 100 human brains; still does not know what a control group of non-autism atypical brains would contain for aluminum content? And that you say alone, discredits and makes void any of the study findings that Exley and his co-authors put forth in this study right here and below? That is directly what you are still trying telling me? Yes or no? I expect a direct answer.

    Aluminium in brain tissue in autism

    Abstract
    Autism spectrum disorder is a neurodevelopmental disorder of unknown aetiology. It is suggested to involve both genetic susceptibility and environmental factors including in the latter environmental toxins. Human exposure to the environmental toxin aluminium has been linked, if tentatively, to autism spectrum disorder. Herein we have used transversely heated graphite furnace atomic absorption spectrometry to measure, for the first time, the aluminium content of brain tissue from donors with a diagnosis of autism. We have also used an aluminium-selective fluor to identify aluminium in brain tissue using fluorescence microscopy. The aluminium content of brain tissue in autism was consistently high. The mean (standard deviation) aluminium content across all 5 individuals for each lobe were 3.82(5.42), 2.30(2.00), 2.79(4.05) and 3.82(5.17) μg/g dry wt. for the occipital, frontal, temporal and parietal lobes respectively. These are some of the highest values for aluminium in human brain tissue yet recorded and one has to question why, for example, the aluminium content of the occipital lobe of a 15 year old boy would be 8.74 (11.59) μg/g dry wt.? Aluminium-selective fluorescence microscopy was used to identify aluminium in brain tissue in 10 donors. While aluminium was imaged associated with neurones it appeared to be present intracellularly in microglia-like cells and other inflammatory non-neuronal cells in the meninges, vasculature, grey and white matter. The pre-eminence of intracellular aluminium associated with non-neuronal cells was a standout observation in autism brain tissue and may offer clues as to both the origin of the brain aluminium as well as a putative role in autism spectrum disorder.

    https://www.sciencedirect.com/science/article/pii/S0946672X17308763

    Amyloid Plaques and Neurofibrillary Tangles
    https://www.brightfocus.org/alzheimers/infographic/amyloid-plaques-and-neurofibrillary-tangles

    New Study: Alzheimer’s & Aluminum Link Can No Longer Be Ignored
    http://www.healthy-holistic-living.com/new-study-alzheimers-aluminum-link-can-no-longer-be-ignored.html

    Elevated brain aluminium and early onset Alzheimer’s disease in an individual occupationally exposed to aluminium: a case report

    Conclusions
    That the individual developed an early onset aggressive form of Alzheimer’s disease suggests a role for aluminium in disease aetiology. That the exposure to aluminium was through occupational exposure to aluminium dust suggests a prominent role for the olfactory system and lungs in the accumulation of aluminium in the brain.

    http://www.jmedicalcasereports.com/content/8/1/41/abstract

    Int J Alzheimers Dis. 2012;2012:914947. doi: 10.1155/2012/914947. Epub 2012 Jul 30.
    Cognitive deterioration and associated pathology induced by chronic low-level aluminum ingestion in a translational rat model provides an explanation of Alzheimer’s disease, tests for susceptibility and avenues for treatment.
    Walton JR.

    Abstract
    A translational aging rat model for chronic aluminum (Al) neurotoxicity mimics human Al exposure by ingesting Al, throughout middle age and old age, in equivalent amounts to those ingested by Americans from their food, water, and Al additives. Most rats that consumed Al in an amount equivalent to the high end of the human total dietary Al range developed severe cognitive deterioration in old age. High-stage Al accumulation occurred in the entorhinal cortical cells of origin for the perforant pathway and hippocampal CA1 cells, resulting in microtubule depletion and dendritic dieback. Analogous pathological change in humans leads to destruction of the perforant pathway and Alzheimer’s disease dementia. The hippocampus is thereby isolated from neocortical input and output normally mediated by the entorhinal cortex. Additional evidence is presented that Al is involved in the formation of neurofibrillary tangles, amyloid plaques, granulovacuolar degeneration, and other pathological changes of Alzheimer’s disease (AD). The shared characteristics indicate that AD is a human form of chronic Al neurotoxicity. This translational animal model provides fresh strategies for the prevention, diagnosis, and treatment of AD.

    http://www.ncbi.nlm.nih.gov/pubmed/22928148

  • Why don’t you block, me?

  • Good luck with that.

  • See my post 5 posts above this one!!!!

  • AutismDadd

    So you recommend aluminum in the brain?

  • AutismDadd

    Call him a pos troll

  • AutismDadd

    The Alzheimer / Autism correlation is interesting. Karl may be well on his way. I’ve purchased my Fiji water and my child chugs it. Fingers crossed it helps.

  • AutismDadd

    He sounds like a castrated CDC employee

  • Karl Wegner MD

    Well they’re central to Bechamp’s theory and they don’t exist. I thought you claimed to understand his theory.

  • Karl Wegner MD

    Flagged.

  • Karl Wegner MD

    And still don’t.

  • Karl Wegner MD

    You’re just too much fun Lowell.

  • Karl Wegner MD

    Thanks

  • Karl Wegner MD

    You don’t have the information Lowell. You don’t even remember what the issue is.

  • Liar. You, fake Karl, have in front of you all of the information and directly in front of you that any honest human being would ever need. It is the same issue that has always been. That, and your demanded denial of it all. So is Karl Wegner MD actually replying on vactruth, from his grave in the cemetery?

  • Flagging goes no where, here, fool.

  • So how is your longstanding personal vendetta going? Looks like you are making a major fool out of yourself, again and again, and like never before. So your directly being made a fool out of here, is fun? It sucks to be you.

  • He adds a new chapter to the understanding of the term, mindless.

  • You can pick for yourself any of the studies that I have reply posted with here, and so far. You will be expected to show refute and directly how and why the study is in error. You can address directly any of the findings and issues that you find in to be in error in the study, and that in regard to such as, materials and methods, results, discussion, and conclusion.

    Furthermore, you as well will be expected to present with any counter studies that have been done, and in which that study has investigated the same or similar issues, and which in that study they find vaccine safety to exist, and regarding the same specific vaccine risk issues, and topic. Get started. You know that you can’t. Prove me wrong?

  • Flagging here is about as worthless for you, as used toilet paper.

  • I heard you the first time, fool. You claim to a lot of things. How about restricting yourself to claiming to what has been stated on this article, and what you can show and prove? And again you can not respond to what I just put in front of you. You refuse to be educated. You want to stay in the dark ages of no existing study science, and right along with Offit and the CDC. Pathetic. And here you are repeatedly continuing to reply, and when you repeatedly have nothing at all. Just packing up and leaving this site would be the best option for you. Actually you have helped me provide a lot more direct information to the public which read these articles, than I ever would have without you. How’s that working out for your sick pro-vax agenda?

  • Karl Wegner MD

    If you had it you’d have posted it a long time ago.

  • Karl Wegner MD

    Why would that be Lowell?

  • Karl Wegner MD

    You keep telling yourself that OK?

  • He certainly has no balls. Just another shill coward with a faked identity.

  • Karl Wegner MD

    You’ve lost track again Lowell. Let me help you. Your challenge is to show the 100 reported previous brain aluminum levels Exley apparently claims to have determined were done with the exact same methods as the current study.

  • Karl Wegner MD

    Why do you think that Lowell?

  • The frightening part of it is that he claims to actually work in the medical field. Sure is again a bad commentary on the pharma based medical field.

  • Karl Wegner MD

    So you don’t want to discuss Bechamp’s theory any more. No one can blame you but you are being a pansy again.

  • AutismDadd

    Their conceit blinds them. They think saying science trumps everything while they ignore science that doesn’t support them and actually trumps their opinions. More and more I can’t be bothered with them except to mock and harass them.

  • Again, Bechamp certainly was a much more biologically and physiologically based scientist, than Pasteur ever was; however this is 2017 and we are much better served currently to move on to the current understandings of science. Something that you again ignored, and could not respond to.

    What do you think of this information; and you can’t respond to that either?

    German Supreme Court Upholds Biologist’s Claim that Measles Virus Does Not Exist
    https://healthimpactnews.com/2017/german-federal-supreme-court-upholds-biologists-claim-that-measles-virus-does-not-exist/

    Pharmaceutical industry lie busted – German Federal Supreme Court ruling confirms: measles virus do not exist http://anonhq.com/pharmaceutical-industry-lie-busted-germa…/ SEE THE COMMENTS
    http://learninggnm.com/SBS/documents/virus-trial.html

    Dr Stefan Lanka | Measles is not a Virus! https://www.youtube.com/watch?v=quwAya3XYsM

    Dr. Stefan Lanka (Snippets) “hiv aids = death?” https://www.youtube.com/watch?v=-btqQa-wXno
    Dr. Stefan Lanka – Why HIV has never been isolated. https://www.youtube.com/watch?v=_ow9rdOdNe0

    Dr. Stefan Lanka: the history of the infection theory (english subtitles) part 1 https://www.youtube.com/watch?v=4p6EoUYrTyQ
    Dr. Stefan Lanka: the history of the infection theory (english subtitles) part 2 https://www.youtube.com/watch?v=Or7lQ58m7i8
    Dr. Stefan Lanka: the history of the infection theory (english subtitles) part 3 https://www.youtube.com/watch?v=aaDcatV38pI

    2001-12 HIV: reality or artefact (1/3) https://www.youtube.com/watch?v=7nIlbllo3s8
    2001-12 HIV: reality or artefact (2/3) https://www.youtube.com/watch?v=xipIb5cYQzs
    2001-12 HIV: reality or artefact (3/3) https://www.youtube.com/watch?v=dW_dNQ0-aSI

    1997-03 Lanka replies to Duesberg (pt1) https://www.youtube.com/watch?v=5SQM-Bu8MZU
    1997-03 Lanka replies to Duesberg (pt2) https://www.youtube.com/watch?v=Qf1OO9jEZzg

    1996-10 Rethinking HIV (pt1) https://www.youtube.com/watch?v=Si8ALIbD-oU
    1996-10 Rethinking HIV (pt2) https://www.youtube.com/watch?v=OO0a1YYM4Vc

    1998-12 Zenger’s nterview with Stefan Lanka (1/5) https://www.youtube.com/watch?v=iTWc824UXis
    1998-12 Zenger’s nterview with Stefan Lanka (2/5) https://www.youtube.com/watch?v=ExB61Ofx6oc
    1998-12 Zenger’s nterview with Stefan Lanka (3/5) https://www.youtube.com/watch?v=RdNAoUIDOw0
    1998-12 Zenger’s nterview with Stefan Lanka (4/5) https://www.youtube.com/watch?v=B5PH9Y19VXQ
    1998-12 Zenger’s nterview with Stefan Lanka (5/5) https://www.youtube.com/watch?v=TbW-uNHmKgU

    Big Bad Viruses will kill you hoax! Virologist says viruses do not exist! https://www.youtube.com/watch?v=_zmdFcAQEJ4
    Stefan Lanka · Snippets from 2001 ‘Deconstructing The Myth of AIDS https://www.youtube.com/watch?v=UsDjth5GJfQ

    ======================================

    Dr. Stefan Lanka: Virologist, Germany. “No particle of HIV has ever been obtained pure, free of contaminants; nor has a complete piece of HIV RNA (or the transcribed DNA) ever been proved to exist.” (Continuum Sept./Oct. 1996)

    Dr. Luc Montagnier, Virologist, discoverer of HIV, Institute Pasteur Paris: “There are too many shortcomings in the theory that HIV causes all signs of AIDS. We are seeing people HIV-infected for 9, 10, 12 years or more, and they are still in good shape, their immune system is still good. It is unlikely that these people will come down with AIDS later.” (Miami Herald 23 Dec. 1990)

    “If there is evidence that HIV causes AIDS, there should be scientific documents which either singly or collectively demonstrate that fact, at least with a high probability. There is no such document.” Dr. Kary Mullis, Biochemist, 1993 Nobel Prize for Chemistry. & co inventor of PCR

    “Up to today there is actually no single scientifically really convincing evidence for the existence of HIV. Not even once such a retrovirus has been isolated and purified by the methods of classical virology.” Dr. Heinz Ludwig Sanger, Emeritus Professor of Molecular Biology and Virology, Max-Planck-Institutes for Biochemistry, Munchen. (Letter to Süddeutsche Zeitung 2000)

  • It is a fact, so just accept it. That, and even though there is no form of thinking reality, that you have ever accepted. Getting desperate, aren’t you.

  • You earlier demanded that I pick one best study aluminum adjuvant related study. I did that and even though they are all good, and as to those I have now posted in front of you in multiple posts. So, now you conveniently forget about that, and move the goal posts again. What a piece of twisted work, you are. Your own challenge was to show evidence that the study I picked was invalid. You failed to do that; so at this point it is actually you that has conveniently lost track, and again.

    And it obviously would not matter if the testing criteria and method was different. Do you actually think that previously donated brains examination was somehow fraudulent and/or irrelevant? How so? You disregarded the most current study, and yet you are claiming that the study was done with diagnostic equipment that is now acceptable to you? So then now you demand that the previous brain examination studies have to have been done exactly the same way, and even though you don’t know how they were done. You sound about as in denial crazed, as a mad monkey chasing its tail.

  • I know that as a fact.

  • Why ask me, ask the editor. And disqus does nothing with it.

  • It has actually been right in front of you since this article was published; within every reply I have made. Yet you have not replied with even as much as a single counter study. Not, one. Just admit that you have no actual vaccine safety study science. Nothing that would be even close to being adequate. That makes for a pretty poor showing on your part.

  • They actually have no vaccine safety science, at all. And certainly as well nothing that would and could ever be considered as adequate.

  • The real pansy could not respond to current day knowledge, and which as well shows a far better way of understanding physiologically based health care, than injecting toxic and contaminated vaccines.

  • Karl Wegner MD

    We know you’re a germ theory denier Lowell. Are you now denying Bechamp’s theory also? And are you now denying viruses exist?

  • Karl Wegner MD

    Well why do you think there’s a flagging option then?

  • Karl Wegner MD

    So now that you’re back with us, you think the study doesn’t need controls because the author claims he studied aluminum levels on other brains with different methods in the past?

  • Karl Wegner MD

    Like chemtrails right?

  • Karl Wegner MD

    Well why does it anger you so much then?

  • Karl Wegner MD

    You haven’t provided evidence Exley used the same methods to calculate aluminum levels in other brains in the past Lowell.

  • Karl Wegner MD

    If “current day knowledge” to you means viruses don’t exist you’re even more looney than I thought.

  • Well, guess what? You can read it for yourself. I don’t create reality and nor the news, I just report it.

    German Supreme Court Upholds Biologist’s Claim that Measles Virus Does Not Exist
    https://healthimpactnews.com/2017/german-federal-supreme-court-upholds-biologists-claim-that-measles-virus-does-not-exist/

    Pharmaceutical industry lie busted – German Federal Supreme Court ruling confirms: measles virus do not exist
    http://anonhq.com/pharmaceutical-industry-lie-busted-german-federal-supreme-court-ruling-confirms-measles-virus-not-exist/

    Dr Stefan Lanka | Measles is not a Virus! https://www.youtube.com/watch?v=quwAya3XYsM

    Citations by HIV – AIDS dissidents
    http://www.virusmyth.com/aids/data2/citations.htm
    http://www.virusmyth.com/aids/controversy.htm

  • Again, I did not say that he used he used the same methods. That does not make the observations and nor the findings, incorrect. You have not provided evidence that in physiological research on it, that no one has ever determined or known what the aluminum content of an atypical brain is, and that to include in regard to Christoher Exley. You still somehow think that there is a chance and probability that normal people are walking around with high levels of aluminum in their brain, and that Exleys findings are actually normal. That is the in denial insanity of your attempted argument.

  • Clearly the only one here that is highly desperate and hot headed angry, is you. I simply accept it as is.

  • So you actually and additionally dumb enough to claim to that chemtrails do not exist, and that you can not determine the difference between a condensation contrail, and a chemtrail? Go back to living within your refusing to face life, denial filled delusions; but some of us are actually informed.

  • The outcome is determined by what the editor chooses to do with that, and how reactive they are, or are not. Why ask me, as I don’t own this site?

  • Again, quite obviously normal atypical brains do not have high levels of aluminum in them, and nor found in high levels in the brain where Exley found that high level of aluminum to exist. The studies I put in front of you put it all together quite well as to the only rational conclusion. Injected vaccines are clearly the cause of that found aluminum in the brain of the autistic.

    What do you not get about the fact that the finding of significant levels aluminum content in the human brain, is not a normal finding?

    No amount of real scientific study would be enough for you; and you must continue to deny it all. You have nothing left to argue but to provide more continued documentary on your own persistent in denial ignorance. You don’t need to be convinced by the way; and no one will ever care if you are. That study and as well the additional studies which have been now done; continue to show a damning picture of what is really going with injected vaccine aluminum adjuvants.

    Do you as well know what polysorbate 80 is? That is as well in the vaccines and which makes the blood/brain barrier more permeable. And what is the result of that? All of the aluminum in the adjuvants and other metallic contamination now known to be in vaccines, can cross right over that blood/brain barrier.

    How Aluminum Nanoparticles in Vaccines Reach the Brain
    http://sanevax.org/how-aluminum-nanoparticles-in-vaccines-reach-the-brain/

    Dirty Vaccines: New Study Reveals Prevalence of Contaminants
    Every Human Vaccine Tested Was Contaminated by Unsafe Levels of Metals and Debris Linked to Cancer and Autoimmune Disease, New Study Reports
    http://info.cmsri.org/the-driven-researcher-blog/dirty-vaccines-new-study-reveals-prevalence-of-contaminants

    Vaccine Papers
    An Objective Look at Vaccine Dangers
    https://vaccinepapers.org/

    And guess what is now known to be firmly attached to the aluminum adjuvant in Gardasil? The HPV DNA contaminant that Merck in the 2006 VRBPAC preapproval document, had earlier told the FDA, was not in the vaccine.

    DNA Contamination in HPV vaccines

    A serious safety issue that should not be swept under the regulatory carpet – Professor Joe Cummins

    When the Human Papilloma Virus (HPV) vaccine Gardasil was recently found to be contaminated with DNA, the US Food and Drug Administration (FDA) lost no time in declaring that the DNA was not a contaminant but a harmless by-product of vaccine production. I disagree; that extraneous DNA is potentially harmful. It should also be noted that the safety and efficacy of HPV vaccines have been controversial from the start (see [1] The HPV Vaccine Controversy and other articles in the series, SiS 41).

    Read more:
    https://www.ga-nz.com/single-post/2016/04/12/A-serious-safety-issue-that-should-not-be-swept-under-the-regulatory-carpet

    Contaminated Gardasil Vaccine May Be Infectious – Potentially Causing Millions More to Become Sick via Blood Transference – Merck Doctor Admits Contaminant Does Not Belong in the Vaccine
    http://sanevax.org/contaminated-gardasil-vaccine-may-be-infectious-potentially-causing-millions-more-to-become-sick-via-blood-transference-merck-doctor-admits-contaminant-does-not-belong-in-the-vaccine/

    Gardasil Contamination: EMA Steps Up to the Plate, FDA drops the Ball
    http://sanevax.org/gardasil-contamination-ema-steps-up-to-the-plate-fda-drops-the-ball/

    Gardasil HPV vaccines found contaminated with recombinant DNA that persists in human blood
    http://sanevax.org/gardasil-hpv-vaccines-found-contaminated-with-recombinant-dna-that-persists-in-human-blood/
    Foreign DNA found in teenager’s blood

    Lab finds HPV DNA in Blood of Gardasil Recipient 2 Years Post-Vaccination HPV (DNA found firmly attached to the aluminum adjuvant, never leaves the body)
    http://sanevax.org/lab-finds-hpv-dna-in-blood-of-gardasil-recipient-2-years-post-vaccination/

    Foreign DNA found in teenager’s blood

    Jasmine, 18, was found dead in her bed in September 2009 six months after her last injection.

    Her mother yesterday outlined Jasmine’s declining health and said after her daughter’s death she became concerned about the vaccine and began research.

    Dr San Hang Lee a pathologist at Milford Hospital in Connecticut gave evidence on the second day of the inquest by videolink.

    He had been sent Jasmine’s post mortem blood and found her blood and spleen were positive for the human papillomavirus, or HPV.

    The Gardasil vaccine is given to prevent some strains of HPV.

    He said it was not the result of a natural HPV infection, most likely the DNA was bound to aluminium which was also found in Jasmine.

    “The HPV gene is foreign DNA and its detection six months after injection is not normal,’’ he told the inquest.

    He said the DNA may cause a reaction that could lead to lethal shock although it was not known if it caused her death but it needed further investigation.

    Read more:
    http://www.stuff.co.nz/dominion-post/news/7445193/Foreign-DNA-found-in-teenagers-blood

    Insight into the cellular fate and toxicity of aluminium adjuvants used in clinically approved human vaccinations, (plus more informative articles)
    http://sanevax.org/research-blog/vaccine-adjuvants-2/

    HPV Vaccine Stakeholders versus Desperate Parents
    http://sanevax.org/hpv-vaccine-stakeholders-versus-desperate-parents/

  • You don’t actually know anything about what I know and believe but what has been previously stereotyped by other shills like yourself, and as well falsely accused. I am all about the available data and the science, and that is all it is about.

  • So you think that somehow atypical/neurotypically normal people are walking around with high levels of aluminum in their brain, and in the same areas that Exley and his research team found that aluminum?

    In your denial you think that regarding this study that there is a yet a chance and probability, that this would be a normal finding?

    You additionally yet think that all of the additional reference studies that I have put in front of you, that those studies are all without applicable irrelevance and in putting it and this situation, all together? Is that correct? Obviously the only reason for that is because you deliberately choose not to; and because you deliberately as well, chose to stay in complete denial.

  • Karl Wegner MD

    Do you believe viruses exist or not?

  • Barzini

    So let’s stop injecting aluminum until those studies have been done

  • Karl Wegner MD

    By not using controls or even using the same techniques in other studies you have no idea if any of his measurements are even accurate.

  • Karl Wegner MD

    Which is why you discourage it so much?

  • Karl Wegner MD

    And 911 was an intentional act by the US government?

  • Karl Wegner MD

    You seem certain that flagging comments on this site is worthless so yes I’m asking you. Why are you certain about that?

  • Karl Wegner MD

    The problem Exley has is that without any kind of controls, and without even using the same methods in other studies, there’s no way to know if his measurements are accurate.

  • Karl Wegner MD

    So you can’t say?

  • Karl Wegner MD

    If Exley wants to get more antivax funding to try to do a proper antivax study I say more power to him.

  • Karl Wegner MD

    Not based on this garbage.

  • Barzini

    OK, you inject your kids and I won’t inject mine

    That way we’re both happy

  • You can’t answer those 6 questions and that is direct evidence that you are unable to be honest and actually debate this articles issues. So it is ONLY Exley’s responsibility and not that of the CDC and Paul Offit? Exley will never be funded by pro-vax sources as they have to much to lose as to what he knows and is continuing to find.

    Again, the question was.

    4. Do you think the CDC should now fund additional follow up studies, and with directly unbiased oversight? If not, why not? Or do you think that the CDC should simply continue to ignore it all?

    So you believe that America’s and the worlds children are not worth doing further study in regard to the potential risk and harm of vaccine aluminum adjuvants. Now we have at least confirmed that much. For you it is all only about defending the false vaccine propaganda, and the many medical careers, and known false authorities that depend on the survival of that propaganda.

    Dr. Paul Offit’s Aluminum Deceptions and Academic Misconduct
    http://vaccinepapers.org/dr-paul-offits-aluminum-deceptions-academic-misconduct/

  • That is not the subject topic or matter which is involved with the article you are posting on. It is irrelevant to the article itself. You have squirmed around and jumped over all this, with enough sick and moving the goal post pranks.

  • You can reword the same false and repeated claim all you want. You have repeatedly been told what the truth is here regarding the validity of that study. Each and every time you ignore it. Again, normal, atypical, neurotypical people are obviously not walking around with a load of aluminum in their brains. To even try to suggest that possibility, is just asinine.

  • Do your own research and figure it out yourself.

  • Discourage what? Your asinine level of falsely accusing stupidity is nothing but a waste of my time to respond to. The truth is the truth, and you were not discouraged from anything. Your continued foolishness here is just that; foolishness.

  • Again, I have already responded to that false claim, repeatedly.

  • Karl Wegner MD

    None of your questions are relevant.

  • Karl Wegner MD

    You don’t want to say I guess. It would put you in a pickle.

  • Karl Wegner MD

    You don’t know what the true levels in Exley’s study were without controls Lowell. No one does.

  • Karl Wegner MD

    You believe it though.

  • Karl Wegner MD

    You discourage flagging comments on this site. You scoff at it. I’d just like to know why.

  • Karl Wegner MD

    You’ve not been able to mount an effective counter-argument despite all your rudeness and copy/pasting.

  • I will simply tell you to do the needed independent research, and decide for yourself. The issue is controversial and again the knowledge and science is clearly not settled. And why can you not respond to the Stefan Lanka information? Your closed mind won’t let you?

    We all know that you are personally crooked, no identity Karl; but that is not what this below information is about.

    There are more important issues. Here is something that is going somewhat viral on facebook right now. You could learn a lot from it.

    This is a two hour informational video. If you want to understand this parents, you need to listen to it at least most of the way through it.

    Are You Crooked? with Forrest Maready,

    This video is brilliant Check out what vaccines are doing on a seriously large scale. This is the close to being the same information that the late Dr. Andrew Moulden put forth.

    https://www.youtube.com/watch?time_continue=51&v=4lf8fdiU1Qk

    Are You Crooked
    http://areyoucrooked.com/

    Dr. Andrew Moulden: Learning to Identify Vaccine Damage
    https://healthimpactnews.com/2015/dr-andrew-moulden-learning-to-identify-vaccine-damage/

    Dr. Andrew Moulden’s Tolerance Lost: Part 1 – “The Problem”
    https://www.youtube.com/watch?v=Re8UI8aCLpM

    Tolerance Lost Vol 1/3 – 1of16 – Moulden
    https://www.youtube.com/watch?v=RZXM-TKvLN8

  • Karl Wegner MD

    Because if you believe viruses exist then Lanka is wrong, and if you deny their existence then Wakefield is a fraud and SV40 in polio vaccines never happened. I hope your head doesn’t explode Lowell.

  • So again you can not answer and nor directly respond to what I actually stated to you. You yourself have not presented with any effective counter-argument in the entire time you have replied on this site. Your level of hypocrisy is as well beyond disgusting.

  • You can flag all you want, it won’t do any good, is all I said. You flag as well and in your blind hypocrisy, for the same exact things that you have repeatedly done yourself. Everyone should be scoffing at that. Does that yet answer your question, why?

  • It is none of your business what I know and believe. This sites articles are about vaccines. Lets see if you can actually ever stay on topic.

  • Karl Wegner MD

    That didn’t cut it either Lowell.

  • Karl Wegner MD

    But why wouldn’t flagging you on this site do any good?

  • Karl Wegner MD

    But demonstrating other crazy things you believe helps explain to others why you have such warped opinions on vaccines.

  • You can be assure they do, and if not that study would never have been published in the Journal of Trace Elements in Medicine and Biology.

    Here are some bed time article stories for you. I think its past your bed time.

    Paging Dr. Offit! Your Aluminum Neurotoxicity Reading Assignments Are Ready
    https://jameslyonsweiler.com/2015/11/16/paging-dr-offit-your-aluminum-neurotoxicity-reading-assignments-are-ready/

    New study: Massive Aluminum levels in Autism brains, is this the smoking gun for vaccines?
    https://medium.com/@jbhandley/new-study-massive-aluminum-levels-in-autism-brains-is-this-the-smoking-gun-for-vaccines-54ae85ec2a9c

    Vaccine Papers
    An Objective Look at Vaccine Dangers
    http://vaccinepapers.org

  • You again are using what you are to create further distraction and disruption away from the subject matters of this article. And again, why could not not respond to the Dr Stefan Lanka virologist, information? Unless you can do that, then as well there is no point to any further discussion on the issue, and as you are evading any and all reference material that exists on the matter. So no, it is actually YOU that is in a pickle; and it is actually you that is a hypocrite.

  • All of those 6 questions are precisely relevant, and i dont know how much more directly obvious that could be. You can not even provide any reason at all as to they are not. Your inability to answer those questions by the way; shows directly not only what kind of liar you are, but as well shows directly how in denial sick, and deliberately deceptive you are.

  • That is not only a lie but a seriously twisted perception. And you do that in your desperation because you can not actually in any honesty directly respond to anything that I have put forth. You are clearly a seriously sick and twisted individual, and that does not help in the vaccine risk debate, one bit.

  • Again, why are you asking me; ask the editor.

  • Nothing ever would, and because all you are is a deflecting, refuse all information and counter arguments, liar.

  • Karl Wegner MD

    How long until they retract it is my question.

  • Karl Wegner MD

    Why would I respond to your Lanka nonsense when you won’t say whether you deny the existence of viruses?

  • Karl Wegner MD

    I can respond to them but it won’t change the fact Exley didn’t use controls.

  • Karl Wegner MD

    Says the guy who believes in chemtrails, 911 as an inside job and faked moon landings.

  • Karl Wegner MD

    Because you say you know. How do you know?

  • Karl Wegner MD

    Not all information – just your information.

  • What a twisted reply. You should have that framed and placed in the pro-vaxers, “Hall of Shame”. So Lanka in your mind is wrong no matter what, and Wakefield was never a fraud on any level. If there are no viruses, you only have your own medical establishment to blame for their misinformation. SV40 could have just as easily happened and even if not actually a virus. My head is focused and calm; and your yours is right now? “LOL”. The pathetic existence of you disgusting shills, is a shocking commentary on humanity, and to say the least.

  • Karl Wegner MD

    Well Lowell if Lanka is right how did Wakefield find measles viruses in children’s intestines? Which one is the fraud?

  • Then you are admitting to being not only highly biased but as well dishonest, and not participating in an honest debate. But we all knew that.

  • I just told you in the previous reply, now move on. No one cares.

  • And you are a warped mind, sick and twisted shill liar, and that is all you will ever be.

  • Karl Wegner MD

    Well that’s one way to interpret it I guess. Another is that all you post is irrelevant garbage you’ve copy/pasted from other antivax sites.

  • No you can’t respond to those questions, as the answers will reveal to much about your lying claim that the study is not showing us directly damning information regarding vaccine aluminum adjuvants.

  • Karl Wegner MD

    We can’t just sweep it all under the rug Lowell.

  • Karl Wegner MD

    Are you denying all those conspiracy theories then? Or am I lying? Which is it?

  • Because and as I already told you that the virus question is unanswered. And yes we can take that question way back to the day of Bechamp and what he put forth. As I said, we now have some serious official information and data, regarding the existence of what is called viruses and as to what actually exists. Again, the science clearly remains as not settled, and as I stated before. Lank puts forth some serious information that you should have paid attention to; but no, that would again destroy all of the false propaganda that you depend on.

  • Karl Wegner MD

    Well it’s not really showing us anything without controls Lowell. But like I said maybe they can do it right next time.

    It sure makes you wonder why they, like the Gatti et al “nanocontamination” group you also love, chose not to use controls.

  • Karl Wegner MD

    Well you can just remain neutral I guess but one of your heroes is a fraud, either Lanka or Wakefield.

  • What normally happens is that the pro-vax side goes in and storm troops the editing staff and demands that the study be retracted no matter what. I don’t think that is going to happen, this time. Exley is not exactly just some average rookie scientist. He as well has been directly studying the aluminum issue for years now.

  • And good luck with that and if only within your own corrupt and warped mind.

  • So now you are desperate enough to go all night here? That figures.

    Well this long reference list of supporting studies surely prove that Wakefield in his 1998 preliminary study, was certainly not a fraud.

    Research References
    http://www.callous-disregard.com/research.htm

  • All you have is only more of the same twisted misinformation and lies, repeat, repeat, repeat. And Gatti as I told you before, did not need controls, as his diagnostic equipment was clearly designed to prevent any question of outside laboratory contamination of the vaccines he tested for metallic contaminants. And still you keep on misinforming and lying about that; and even though I directly copied and pasted that information to you.

  • So you don’t even know if you are telling the truth, or lying. As well to be only an unproven conspiracy theory, there must be no direct evidence. Your mind obviously does not process direct evidence, but only what you in your closed and small mind can handle That is called being a SHEOPLE.

  • Actually, that is all you ever do is sweep everything under the rug, you hypocrite.

  • Everyone can now see the misinformation and the lies you present with, thanks to me.

  • Anna Watson

    It is relevant asking about controls of course… I would like to see controls added to vaccine safety testing to begin to look at the heath outcomes of the vaccinated and unvaccinated….

    But regarding this research, it is relevant that a ‘normal’ range of aluminium has been established? The issue is to have a greater sample to see how neurological conditions correlate or not to the levels of aluminium

    “The aluminium concentration for 7 normal human brains was 1-9 +/- 0-7 SD mug/g dry weight (n = 208 samples). ”

    https://www.ncbi.nlm.nih.gov/pubmed/963531

    I am guessing that there will be cases of autism and alzheimer’s with ‘normal’ levels of aluminium but more research needs to show that aluminium is not only associated but also causal. With what we know about the toxicity of aluminium and the neurological effects then it makes sense surely to reduce the aluminium as a matter of caution at the very least.

  • Karl Wegner MD

    What normally happens is the journal editors get embarrassed reading all the criticism about some garbage paper they didn’t properly review, and they retract it.

  • Karl Wegner MD

    Well that doesn’t require luck but thanks.

  • Karl Wegner MD

    Then it must be Lanka.

  • Karl Wegner MD

    Both studies are fatally flawed due to the lack of controls.

  • Karl Wegner MD

    You believe lots of things without direct evidence.

  • Karl Wegner MD

    If you ever posted anything credible things might be different.

  • Karl Wegner MD

    Just keep living in that personal fantasy.

  • You, truth, facts, and reality, simply do not blend to together very well for you, do they.

  • Said by person that has himself posted nothing at all that comes from the realm of scientific study. You clearly don’t even care what the vaccine harm risks are. It remains for you all only about making endless denial.

  • Obviously you do not even comprehend as much as what direct evidence, is. You chose to remain a sheople, no matter what

  • You have already had it explained to you multiple times why that is not true. Yet you just keep on misinforming and lying about it

  • Yet in that claim you can not explain why Dr Stefan Lanka virologist’s said findings are incorrect. You are actually the worst shill debater of all time. No one cares about the need for your maintained denial.

  • So you don’t even understand as much as the use of sarcasm?

  • That is certainly a warped opinion and view on it all, and as to what actually takes place. Yet you can not defend anything at all here, and that with actual facts.

  • Karl Wegner MD

    Lowell one of the hallmarks of psychosis is the inability to distinguish reality from fantasy. You should get help.

  • Karl Wegner MD

    You know the risk of serious vaccine adverse effects is less than 1 per million doses, yet you keep lying about it. Why?

  • Karl Wegner MD

    Direct evidence clearly shows us you’re not cut out for this.

  • Karl Wegner MD

    Oh you’ve huffed and puffed but you just can’t explain away the lack of controls.

  • Karl Wegner MD

    Since you insist Wakefield’s claim of finding measles viruses in children’s intestines is incontrovertible then by definition Lanka must be a fraud. Or do you want to flip flop?

  • Karl Wegner MD

    Oh you scoundrel you were using sarcasm

  • Karl Wegner MD

    So it must be storm troopers

  • Maybe what he found is not a virus after all. You have to actually think, here.

  • Having provided and studied the brains from cadeavor controls with no diagnosed autism, and that having been done in that study, or not; the point is here that normal levels of aluminum in the atypical/neurotypical brain, have clearly and previously been studied and determined. Thus this study still remains as a damning commentary on the use of vaccine aluminum adjuvants, and the serious need to do further follow up studies. And you are as said, still opposed to doing those studies? No need for CDC funding of further follow up studies?

    Brain. 1976 Mar;99(1):67-80.
    Aluminium, neurofibrillary degeneration and Alzheimer’s disease.
    Crapper DR, Krishnan SS, Quittkat S.

    Abstract
    Aluminium is neurotoxic and results in the proliferation of 100 A diameter filaments in the cytoplasm of certain neurons. The aluminium concentration for 7 normal human brains was 1-9 +/- 0-7 SD mug/g dry weight (n = 208 samples). The aluminium content of 585 areas sampled in 10 post-mortem cases of Alzheimer’s disease ranging in age from 50 to 88 years, in which the diagnosis was based on the specific histological appearances, revealed an elevated aluminium content in some regions. A range of 0-4 – 107-0 mug/g was encountered and 28 per cent of all regions sampled had concentrations in excess of 4 mug/g. Five of 6 cerebral biopsies from patients with Alzheimer’s disease also had elevated aluminium content. In 2 additional Alzheimer’s brains with neurofibrillary degeneration restricted to certain anatomical areas, elevated aluminium content was found to be associated with neurofibrillary degeneration and not with senile plaques. Furthermore, elevated aluminium content in multiple cortical regions was not found in 2 vascular dementias of the elderly. While the cytotoxic concentration for human neurons is unknown, the cytotoxic concentration for cat’s cerebral neurons appears to lie between 4 and 6 mug/g dry weight.

    https://www.ncbi.nlm.nih.gov/pubmed/963531

    Aluminium in brain tissue in autism

    Abstract
    Autism spectrum disorder is a neurodevelopmental disorder of unknown aetiology. It is suggested to involve both genetic susceptibility and environmental factors including in the latter environmental toxins. Human exposure to the environmental toxin aluminium has been linked, if tentatively, to autism spectrum disorder. Herein we have used transversely heated graphite furnace atomic absorption spectrometry to measure, for the first time, the aluminium content of brain tissue from donors with a diagnosis of autism. We have also used an aluminium-selective fluor to identify aluminium in brain tissue using fluorescence microscopy. The aluminium content of brain tissue in autism was consistently high. The mean (standard deviation) aluminium content across all 5 individuals for each lobe were 3.82(5.42), 2.30(2.00), 2.79(4.05) and 3.82(5.17) μg/g dry wt. for the occipital, frontal, temporal and parietal lobes respectively. These are some of the highest values for aluminium in human brain tissue yet recorded and one has to question why, for example, the aluminium content of the occipital lobe of a 15 year old boy would be 8.74 (11.59) μg/g dry wt.? Aluminium-selective fluorescence microscopy was used to identify aluminium in brain tissue in 10 donors. While aluminium was imaged associated with neurones it appeared to be present intracellularly in microglia-like cells and other inflammatory non-neuronal cells in the meninges, vasculature, grey and white matter. The pre-eminence of intracellular aluminium associated with non-neuronal cells was a standout observation in autism brain tissue and may offer clues as to both the origin of the brain aluminium as well as a putative role in autism spectrum disorder.

    3. Results
    3.1. Aluminium content of brain tissues
    The aluminium content of all tissues ranged from 0.01 (the limit of quantitation) to 22.11 μg/g dry wt. (Table 1). The aluminium content for whole brains (n = 4 or 5 depending upon the availability of hippocampus tissue) ranged from 1.20 (1.06) μg/g dry wt. for the 44 year old female donor (A1) to 4.77 (4.79) μg/g dry wt. for a 33 year old male donor (A5). Previous measurements of brain aluminium, including our 60 brain study [13], have allowed us to define loose categories of brain aluminium content beginning with ≤1.00 μg/g dry wt. as pathologically benign (as opposed to ‘normal’). Approximately 40% of tissues (24/59) had an aluminium content considered as pathologically-concerning (≥2.00 μg/g dry wt.) while approximately 67% of these tissues had an aluminium content considered as pathologically-significant (≥3.00 μg/g dry wt.). The brains of all 5 individuals had at least one tissue with a pathologically-significant content of aluminium. The brains of 4 individuals had at least one tissue with an aluminium content ≥5.00 μg/g dry wt. while 3 of these had at least one tissue with an aluminium content ≥10.00 μg/g dry wt. (Table 1). The mean (SD) aluminium content across all 5 individuals for each lobe were 3.82(5.42), 2.30(2.00), 2.79(4.05) and 3.82(5.17) μg/g dry wt. for the occipital, frontal, temporal and parietal lobes respectively. There were no statistically significant differences in aluminium content between any of the 4 lobes.

    Read more:
    https://www.sciencedirect.com/science/article/pii/S0946672X17308763

    Exley’s previous study.

    Aluminium, iron and copper in human brain tissues donated to the
    medical research council’s cognitive function and ageing study
    Emily House,a Margaret Esiri,b Gill Forster,c Paul G Incec and
    Christopher Exley*a Accepted 14th October 2011

    Aluminium, iron and copper are all implicated in the aetiology of neurodegenerative diseases including Alzheimer’s disease. However, there are very few large cohort studies of the content of
    these metals in aged human brains. We have used microwave digestion and TH GFAAS to measure aluminium, iron and copper in the temporal, frontal, occipital and parietal lobes of 60 brains donated to the Cognitive Function and Ageing Study. Every precaution was taken to reduce contamination of samples and acid digests to a minimum. Actual contamination was estimated by preparing a large number of (170+) method blanks which were interspersed within the full set of 700+ tissue digests. Subtraction of method blank values (MBV) from tissue digest values resulted in metal contents in all tissues in the range, MBV to 33 mg g1 dry wt. for aluminium, 112 to 8305 mg g1 dry wt. for iron and MBV to 384 mg g1 dry wt. for copper. While the median aluminium content for all tissues was 1.02 mg g1 dry wt. it was informative that 41 brains out of 60 included at least one tissue with an aluminium content which could be considered as potentially pathological (4 3.50 mg g1 dry wt.). The median content for iron was 286.16 mg g1 dry wt. and overall tissue iron contents were generally high which possibly reflected increased brain iron in ageing and in neurodegenerative disease. The median content for copper was 17.41 mg g1 dry wt. and overall tissue copper contents were lower than expected for aged brains but they were commensurate with aged brains showing signs of neurodegenerative disease. In this study we have shown, in particular, the value of carrying out significant numbers of method blanks to identify unknown sources of contamination. When these values are subtracted from tissue digest values the absolute metal contents could be considered as conservative and yet they may still reflect aspects of ageing and neurodegenerative disease in individual brains.

    Read more:
    https://pdfs.semanticscholar.org/cffe/16976a373a858d365a1d18d42bebb6d59181.pdf

    https://www.ncbi.nlm.nih.gov/pubmed/22045115

  • Get back to the vaccine related issues in regard to this article, or get gone. There is no need to respond to such continued and only falsely harassing, childish nonsense.

  • The truth is that everyone can now see what a low level of mentality, twisted liar you are. You never have anything, and yet you falsely claim to be the winner of every attempted debate that you have ever been in.

  • You have seen me directly refute that claim before, and with the real data. Yet you present again with the same false claim. There are no lies on my part, but only facts and reference. You are the person that is actually lying about it. And you know you are.

  • Coming from the person with the real in denial psychosis; and which can not determine fiction from truth, and nor reality, from deliberate ignorance, and sheople fantasy.

  • That study only adds more direct evidence to that the atypical/neurotypical; and regarding otherwise normal brain levels of aluminum, (and as to that data), that-that information is found be well known and within the field of brain study science. With that being known, then the significance of not including a non-autistic donated, aluminum content comparative brain study as well, then becomes far less significant.

  • Karl Wegner MD

    OK then it’s Wakefield who is the fraud.

  • Karl Wegner MD

    The point here is that without controls no one knows if their measurements are accurate or how they compare to non-autistic brains.

    And BTW the aluminum-Alzheimer’s association is no longer believed.

  • Karl Wegner MD

    It was your claim Lowell.

  • Karl Wegner MD

    Not every debate – just every debate with you.

  • Karl Wegner MD

    There’s a difference between refuting claims and denying facts – you only do the latter.

  • Karl Wegner MD

    Truth is different from reality then?

  • Ron Roy

    Shill! Go ahead and flag me too.

  • They are of course one and the same.

  • You have no facts, and I have repeatedly shown that to be the case. When was the last time you posted a scientific study that counters any of the studies that I have replied with? You have not posted anything at all. So, where are your facts?

  • That is correct, you have lost every debate that you have ever had with me. Just face it.

  • Then just keep on begging the devil to help big pharma throw enough shillary wrenches at that study, to get it retracted. Good luck with that. By the way, when is the CDC going to address this, and fund an obviously needed follow up study? You should know as well that they obviously do not care about vaccine safety. The vaccine truth will destroy them.

    Brain. 1976 Mar;99(1):67-80.
    Aluminium, neurofibrillary degeneration and Alzheimer’s disease.
    Crapper DR, Krishnan SS, Quittkat S.

    Abstract
    Aluminium is neurotoxic and results in the proliferation of 100 A diameter filaments in the cytoplasm of certain neurons. The aluminium concentration for 7 normal human brains was 1-9 +/- 0-7 SD mug/g dry weight (n = 208 samples). The aluminium content of 585 areas sampled in 10 post-mortem cases of Alzheimer’s disease ranging in age from 50 to 88 years, in which the diagnosis was based on the specific histological appearances, revealed an elevated aluminium content in some regions. A range of 0-4 – 107-0 mug/g was encountered and 28 per cent of all regions sampled had concentrations in excess of 4 mug/g. Five of 6 cerebral biopsies from patients with Alzheimer’s disease also had elevated aluminium content. In 2 additional Alzheimer’s brains with neurofibrillary degeneration restricted to certain anatomical areas, elevated aluminium content was found to be associated with neurofibrillary degeneration and not with senile plaques. Furthermore, elevated aluminium content in multiple cortical regions was not found in 2 vascular dementias of the elderly. While the cytotoxic concentration for human neurons is unknown, the cytotoxic concentration for cat’s cerebral neurons appears to lie between 4 and 6 mug/g dry weight.

    https://www.ncbi.nlm.nih.gov/pubmed/963531

    Aluminium in brain tissue in autism

    Abstract
    Autism spectrum disorder is a neurodevelopmental disorder of unknown aetiology. It is suggested to involve both genetic susceptibility and environmental factors including in the latter environmental toxins. Human exposure to the environmental toxin aluminium has been linked, if tentatively, to autism spectrum disorder. Herein we have used transversely heated graphite furnace atomic absorption spectrometry to measure, for the first time, the aluminium content of brain tissue from donors with a diagnosis of autism. We have also used an aluminium-selective fluor to identify aluminium in brain tissue using fluorescence microscopy. The aluminium content of brain tissue in autism was consistently high. The mean (standard deviation) aluminium content across all 5 individuals for each lobe were 3.82(5.42), 2.30(2.00), 2.79(4.05) and 3.82(5.17) μg/g dry wt. for the occipital, frontal, temporal and parietal lobes respectively. These are some of the highest values for aluminium in human brain tissue yet recorded and one has to question why, for example, the aluminium content of the occipital lobe of a 15 year old boy would be 8.74 (11.59) μg/g dry wt.? Aluminium-selective fluorescence microscopy was used to identify aluminium in brain tissue in 10 donors. While aluminium was imaged associated with neurones it appeared to be present intracellularly in microglia-like cells and other inflammatory non-neuronal cells in the meninges, vasculature, grey and white matter. The pre-eminence of intracellular aluminium associated with non-neuronal cells was a standout observation in autism brain tissue and may offer clues as to both the origin of the brain aluminium as well as a putative role in autism spectrum disorder.

    3. Results
    3.1. Aluminium content of brain tissues
    The aluminium content of all tissues ranged from 0.01 (the limit of quantitation) to 22.11 μg/g dry wt. (Table 1). The aluminium content for whole brains (n = 4 or 5 depending upon the availability of hippocampus tissue) ranged from 1.20 (1.06) μg/g dry wt. for the 44 year old female donor (A1) to 4.77 (4.79) μg/g dry wt. for a 33 year old male donor (A5). Previous measurements of brain aluminium, including our 60 brain study [13], have allowed us to define loose categories of brain aluminium content beginning with ≤1.00 μg/g dry wt. as pathologically benign (as opposed to ‘normal’). Approximately 40% of tissues (24/59) had an aluminium content considered as pathologically-concerning (≥2.00 μg/g dry wt.) while approximately 67% of these tissues had an aluminium content considered as pathologically-significant (≥3.00 μg/g dry wt.). The brains of all 5 individuals had at least one tissue with a pathologically-significant content of aluminium. The brains of 4 individuals had at least one tissue with an aluminium content ≥5.00 μg/g dry wt. while 3 of these had at least one tissue with an aluminium content ≥10.00 μg/g dry wt. (Table 1). The mean (SD) aluminium content across all 5 individuals for each lobe were 3.82(5.42), 2.30(2.00), 2.79(4.05) and 3.82(5.17) μg/g dry wt. for the occipital, frontal, temporal and parietal lobes respectively. There were no statistically significant differences in aluminium content between any of the 4 lobes.

    Read more:
    https://www.sciencedirect.com/science/article/pii/S0946672X17308763

    Exley’s previous study.

    Aluminium, iron and copper in human brain tissues donated to the
    medical research council’s cognitive function and ageing study
    Emily House,a Margaret Esiri,b Gill Forster,c Paul G Incec and
    Christopher Exley*a Accepted 14th October 2011

    Aluminium, iron and copper are all implicated in the aetiology of neurodegenerative diseases including Alzheimer’s disease. However, there are very few large cohort studies of the content of
    these metals in aged human brains. We have used microwave digestion and TH GFAAS to measure aluminium, iron and copper in the temporal, frontal, occipital and parietal lobes of 60 brains donated to the Cognitive Function and Ageing Study. Every precaution was taken to reduce contamination of samples and acid digests to a minimum. Actual contamination was estimated by preparing a large number of (170+) method blanks which were interspersed within the full set of 700+ tissue digests. Subtraction of method blank values (MBV) from tissue digest values resulted in metal contents in all tissues in the range, MBV to 33 mg g1 dry wt. for aluminium, 112 to 8305 mg g1 dry wt. for iron and MBV to 384 mg g1 dry wt. for copper. While the median aluminium content for all tissues was 1.02 mg g1 dry wt. it was informative that 41 brains out of 60 included at least one tissue with an aluminium content which could be considered as potentially pathological (4 3.50 mg g1 dry wt.). The median content for iron was 286.16 mg g1 dry wt. and overall tissue iron contents were generally high which possibly reflected increased brain iron in ageing and in neurodegenerative disease. The median content for copper was 17.41 mg g1 dry wt. and overall tissue copper contents were lower than expected for aged brains but they were commensurate with aged brains showing signs of neurodegenerative disease. In this study we have shown, in particular, the value of carrying out significant numbers of method blanks to identify unknown sources of contamination. When these values are subtracted from tissue digest values the absolute metal contents could be considered as conservative and yet they may still reflect aspects of ageing and neurodegenerative disease in individual brains.

    Read more:
    https://pdfs.semanticscholar.org/cffe/16976a373a858d365a1d18d42bebb6d59181.pdf

    https://www.ncbi.nlm.nih.gov/pubmed/22045115

  • Same false claims, different day.

    How is this study an Alzheimers Association study?

    Brain. 1976 Mar;99(1):67-80.
    Aluminium, neurofibrillary degeneration and Alzheimer’s disease.
    Crapper DR, Krishnan SS, Quittkat S.

    Abstract
    Aluminium is neurotoxic and results in the proliferation of 100 A diameter filaments in the cytoplasm of certain neurons. The aluminium concentration for 7 normal human brains was 1-9 +/- 0-7 SD mug/g dry weight (n = 208 samples). The aluminium content of 585 areas sampled in 10 post-mortem cases of Alzheimer’s disease ranging in age from 50 to 88 years, in which the diagnosis was based on the specific histological appearances, revealed an elevated aluminium content in some regions. A range of 0-4 – 107-0 mug/g was encountered and 28 per cent of all regions sampled had concentrations in excess of 4 mug/g. Five of 6 cerebral biopsies from patients with Alzheimer’s disease also had elevated aluminium content. In 2 additional Alzheimer’s brains with neurofibrillary degeneration restricted to certain anatomical areas, elevated aluminium content was found to be associated with neurofibrillary degeneration and not with senile plaques. Furthermore, elevated aluminium content in multiple cortical regions was not found in 2 vascular dementias of the elderly. While the cytotoxic concentration for human neurons is unknown, the cytotoxic concentration for cat’s cerebral neurons appears to lie between 4 and 6 mug/g dry weight.

    https://www.ncbi.nlm.nih.gov/pubmed/963531

    Provide the evidence that the so called Alzheimer’s Association is no longer believed, and by whom, and in regard to what?

  • No, it is you that is the real fraud.

  • Why are you still using the false identity of a deceased MD?

    Dr. Karl H. Wegner
    1930 – 2014 Obituary
    http://www.legacy.com/obituaries/argusleader/obituary.aspx?pid=170508529

    For the readers.

    The vaccine harm done answers have been there all along; the answers that the CDC and the pro-vaccinator’s like fake Karl here, continue to refuse.

    Dr. Andrew Moulden: Learning to Identify Vaccine Damage
    https://vaccineimpact.com/2015/dr-andrew-moulden-learning-to-identify-vaccine-damage/

    Dr. Andrew Moulden’s Tolerance Lost: Part 1 – “The Problem”
    https://www.youtube.com/watch?v=Re8UI8aCLpM

    Tolerance Lost Vol 1/3 – 1 of 16 – Moulden
    https://www.youtube.com/watch?v=RZXM-TKvLN8

    Health Canada Corruption – Dr. Andrew Moulden

    Dr. Andrew Moulden getting the message of truth out to people about the extreme corporate corruption of Health Canada, the FDA, and other corporate controlled medical care entities that are, in fact, destroying peoples health with vaccines and other chemical pharmaceutical drugs.

    https://www.dailymotion.com/video/xbo5vf

    Are You Crooked? (Forrest Maready)
    https://www.youtube.com/watch?v=4lf8fdiU1Qk

    ARE YOU CROOKED?
    What our faces are trying to tell us.
    http://areyoucrooked.com/

  • Bored Now

    or more specifically that the amount of variability between controls and non-neurotypical cases was significant before we go off and claim causation. Also even if there was some 100-brain study done on neurotypticals n=100 probably isn’t enough to establish a useful baseline. The mean is just too easy to influence.

  • Bored Now

    …or what “high levels of aluminum”” actually means in any useful sense of the term.

  • Karl Wegner MD

    You need to work on your wording then.

  • Karl Wegner MD

    Well Lowell, if the risk of serious vaccine adverse effects isn’t less than 1 in a million, what is it? Please be specific and please explain how you calculated it. (you won’t)

  • Karl Wegner MD

    Reading comprehension Lowell – work on it.

  • Karl Wegner MD

    You think the CDC should fund a follow up study to the one on cat brains from 1976?

  • Karl Wegner MD

    Lol Lowell – an Alzheimer’s Association study?

  • Karl Wegner MD

    You’ve gotten yourself in a bind haven’t you? Now all you can do is lash out.

  • Karl Wegner MD

    So did you send Moulden pictures of your face and a few hundred dollars Lowell?

  • Actually it has nothing to do with me. That work involves scientific study that is so far over and above your head that a sheople person like you is simply unable to comprehend it.

    Guess what popped back up on the internet today? You are going to have to grit your teeth, and stomp your feet.

    High Levels of Aluminum Found in Children with Autism
    http://www.dirtybigpharmatruth.com/high-levels-of-aluminum-found-in-autistic-childrens-brain-tissue.html

  • The only really blind haven going on is as to you and what exists at the FDA, CDC, and the WHO. Paul Offit as well exists within a mindless blind haven of deliberate ignorance and as well no actual vaccine safety study science. You can find what you are not looking for and nor the truth currently or historically. You can denu it and lie about it all you want.

    Again, guess what popped back up on the internet today? You are going to have to grit your teeth, and stomp your feet. This page directly corresponds to the article right here that you are posting on.

    High Levels of Aluminum Found in Children with Autism
    http://www.dirtybigpharmatruth.com/high-levels-of-aluminum-found-in-autistic-childrens-brain-tissue.html

  • You directly made the said accusation so clarify it and as to what you stated.

    Why are you remaining in the dark ages when the science already shows us what is going on?

    Aluminum, Interleukin-6, and Brain Inflammation

    A central thesis of the Vaccine Papers blog is that aluminum adjuvant causes brain injury and autism by an immune activation mechanism. Specifically, the hypothesis is that aluminum adjuvant causes autism by inducing interleukin-6 (IL-6) production in the brain. Elevated IL-6 causes autism.

    There is strong evidence for this hypothesis, but we do not yet have conclusive experimental results showing that Al adjuvant induces IL-6 (and/or IL-17a) in the brain. Instead we have experiments showing 1) soluble aluminum induces IL-6 in the brain and other tissues, and 2) Al adjuvant causes inflammation/microglial activation in the brain. Some of these studies use aluminum adjuvant dosages essentially the same as dosages infants receive according to the CDC schedule.

    A Special Relationship Between Aluminum and IL-6?
    Aluminum strongly induces IL-6, and there are good scientific reasons why. Aluminum causes oxidation, and IL-6 is produced in response to oxidative stress (e.g., low glutathione, elevated free radicals). IL-6 stimulates tissue repair and healing of oxidation injury.

    One way aluminum likely induces oxidation is by displacing iron from a protein (transferrin) where iron is safely stored. Transferrin is specifically designed to bind iron and prevent it from causing oxidation. Free (unbound) iron floating around is very toxic, because its a potent catalyst for oxidation reactions. So, one way aluminum induces oxidation is by unleashing free iron. In living cells, free iron creates an explosion of destructive oxidation.

    One way aluminum likely induces oxidation is by displacing iron from a protein (transferrin) where iron is safely stored. Transferrin is specifically designed to bind iron and prevent it from causing oxidation. Free (unbound) iron floating around is very toxic, because its a potent catalyst for oxidation reactions. So, one way aluminum induces oxidation is by unleashing free iron. In living cells, free iron creates an explosion of destructive oxidation.

    The Viezeliene et al. paper (described below) states:

    Read more:
    http://vaccinepapers.org/aluminum-inflammation-interleukin-6/

    THE PRO-OXIDANT ACTIVITY OF ALUMINUM
    CHRISTOPHER EXLEY

    Birchall Centre for Inorganic Chemistry and Materials Science, Keele University, Staffordshire, UK
    (Received 21 August 2003; Revised 17 November 2003; Accepted 20 November 2003)
    Abstract—Aluminum, a non-redox-active metal is, nevertheless, a pro-oxidant both in in vitro preparations and in vivo.
    It facilitates both superoxide- and iron-driven biological oxidation by mechanisms that remain to be resolved. More than
    10 years ago Fridovich and colleagues suggested that the facilitation of superoxide-driven biological oxidation by
    aluminum was due to an interaction between the metal and the superoxide radical anion (Free Radic. Biol. Med. 13:79 –
    81; 1992). This thesis has been examined herein and it is concluded that much, if not all, of the pro-oxidant activity of
    aluminum might be explained by the formation of an aluminum superoxide semireduced radical ion. D 2003 Elsevier
    Inc.

    http://vaccinepapers.org/wp-content/uploads/The-pro-oxidant-activity-of-aluminum.pdf

    New Kid On The Block: IL-17a

    Click for list of papers in this post.

    An important new paper (January 2016) by Choi et al. in the well-known journal Science provides valuable new information about how IL-6 causes autism. This paper reports that IL-6 causes autism by inducing production of the cytokine IL-17a.

    Paper (Choi):The maternal interleukin-17a pathway in mice promotes autismlike phenotypes in offspring

    In biochemistry and biology, there are “signalling pathways” that have multiple steps connected in a chain. There can be many steps in a signaling pathway. Cytokines often act this way. So, when we say that “IL-6 causes autism”, it could mean that IL-6 acts directly, or that the IL-6 triggers something else that causes autism.

    The new discovery is that IL-17a acts downstream of IL-6 to cause autism. In other words, IL-17a production is an intermediate step between IL-6 production and autism. So, Choi et al provides both a confirmation and extension of IL-6-autism causality. No wonder this paper was published in one of the most important scientific journals in the world.

    IL-17a is involved in autoimmune diseases, crohns disease, rheumatoid arthritis, multiple sclerosis and asthma for example. Its a really important cytokine associated with its own type of T-helper cell (Th17 cells). It was discovered in 1993. Here is a review paper on IL-17a: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2826676/

    Choi et al. also performed a replication experiment demonstrating that maternal IL-6 injection causes autistic behavior in mice. So the IL-6-autism discovery has been replicated again.

    Read more:
    http://vaccinepapers.org/new-kid-block-il-17a/

    Immunology. 2010 Mar
    Interleukin-17 and its target genes: mechanisms of interleukin-17 function in disease
    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2826676/

    And by the way, it is not only aluminum adjuvants that are triggering autism and vaccine injury. There are as well several other vaccine associated factors. Live virus vaccines, an overload of cytokine activity due to to many vaccines being injected at one time. The use of aborted fetal cells to grow the antigens on, and with resulting injected short and long chain DNA contamination. And of course mercury as well was a contributing factor, along with now known metallic contaminants in the vaccines. How are those said contaminants getting in there; tell me and if you are at such a rocket scientist level of understanding in health care?

    Dirty Vaccines: New Study Reveals Prevalence of Contaminants

    Every Human Vaccine Tested Was Contaminated by Unsafe Levels of Metals and Debris Linked to Cancer and Autoimmune Disease, New Study Reports

    Researchers examining 44 samples of 30 different vaccines found dangerous contaminants, including red blood cells in one vaccine and metal toxicants in every single sample tested – except in one animal vaccine.

    Using extremely sensitive new technologies not used in vaccine manufacturing, Italian scientists reported they were “baffled” by their discoveries which included single particles and aggregates of organic debris including red cells of human or possibly animal origin and metals including lead, tungsten, gold, and chromium, that have been linked to autoimmune disease and leukemia.

    In the study, published this week in the International Journal of Vaccines and Vaccination, the researchers led by Antonietta Gatti, of the National Council of Research of Italy and the Scientific Director of Nanodiagnostics, say their results “show the presence of micro- and nano-sized particulate matter composed of inorganic elements in vaccine samples” not declared in the products’ ingredients lists.

    Lead particles were found in the cervical cancer vaccines, Gardasil and Cervarix, for example, and in the seasonal flu vaccine Aggripal manufactured by Novartis as well as in the Meningetec vaccine meant to protect against meningitis C.

    Samples of an infant vaccine called Infarix Hexa (against diphtheria, tetanus, pertussis, hepatitis B, poliomyelitis and haemophilus influenzae type B) manufactured by GlaxoSmithKline was found to contain stainless steel, tungsten and a gold-zinc aggregate.

    Other metal contaminants included platinum, silver, bismuth, iron, and chromium. Chromium (alone or in alloy with iron and nickel) was identified in 25 of the human vaccines from Italy and France that were tested.

    GSK’s Fluarix vaccine for children three years and older contained 11 metals and aggregates of metals. Similar aggregates to those identified in the vaccines have been shown to be prevalent in cases of leukemia, the researchers noted.

    Many of the vaccines contained iron and iron alloys which, according to the researchers, “can corrode and the corrosion products exert a toxicity affecting the tissues”.

    READ MORE:
    http://info.cmsri.org/the-driven-researcher-blog/dirty-vaccines-new-study-reveals-prevalence-of-contaminants

    Dirty Vaccines – Part Two: What the Industry Knows and Isn’t Telling You
    http://www.greenmedinfo.com/blog/dirty-vaccines-part-two-what-industry-knows-and-isnt-telling-you

    Breaking Interview: Lead Author of ‘Dirty Vaccines’ Study Speaks Out
    http://www.greenmedinfo.com/blog/breaking-interview-lead-author-dirty-vaccines-study-speaks-out

    Vaccine Contaminants, Nanotechnology, and Cancer
    http://vaxxter.com/vaccine_contaminants_nano_cancer/

    Metals Debris Found in Vaccine Supply
    http://www.ecowatch.com/kennedy-metal-debris-vaccines-2276687112.html

    New Quality-Control Investigations on Vaccines: Microand
    Nanocontamination
    http://medcraveonline.com/IJVV/IJVV-04-00072.pdf

    Lead, Iron, Chromium and Other Metals Routinely Contaminate Vaccine Adjuvants, Industry Study Reports
    http://info.cmsri.org/aluminum-and-your-health-blog/lead-iron-chromium-and-other-metals-routinely-contaminate-vaccine-adjuvants-industry-study-reports?utm_campaign=eBook%3A+Age+of+Aluminum&utm_content=46490849&utm_medium=social&utm_source=facebook

    Little Things Matter: The Impact of Toxins on the Developing Brain
    Canadian Environmental Health Atlas

    We’ve been studying the impact of toxins on children for the past 30 years and reached the inescapable conclusion: little things matter. We’ve discovered that extremely low levels of toxins can impact brain development. We have also discovered that subtle shifts in the intellectual abilities of individual children have a big impact on the number of children in a population that are challenged or gifted. Steps should be taken to reduce children’s exposure to toxins or suspected toxins. You can read more about how toxins impact brain development and the supportive documentation for this video here:

    https://www.youtube.com/watch?v=E6KoMAbz1Bw

    Vaccine contaminated with short and long chain DNA fragments when the antigen is grown on aborted fetal cell tissue. Many vaccines today are made that way.

    STUDIES AND RESEARCHES ON AUTISM DISORDERS
    http://soundchoice.org/autism/

    Research and Publications
    http://soundchoice.org/autism/autism-research/

    New CDC Guidelines: 5 Year-Old Can Receive up to 19 Vaccinations in One Month
    http://vaccineimpact.com/2017/new-cdc-guidelines-5-year-old-can-receive-up-to-19-vaccinations-in-one-month/

    Vaccine Schedules
    https://www.cdc.gov/vaccines/schedules/index.html

    Big Pharma and Big Profits: The Multibillion Dollar Vaccine Market
    New Report says “Vaccine Market” Worth $61 Billion by 2020
    https://www.globalresearch.ca/big-pharma-and-big-profits-the-multibillion-dollar-vaccine-market/5503945

    How Much Money Do Pediatricians Really Make From Vaccines?
    https://wellnessandequality.com/tag/blue-cross-blue-shields-physician-incentive-program/

    2017 Performance
    Recognition Program
    PROVIDER INCENTIVE PROGRAM FOR:
    • BCN Commercial HMO
    • BCN AdvantageSM HMO-POS
    • BCBSM Medicare Plus BlueSM PPO

    http://thephysicianalliance.org/images/FilesDocuments/2017_BCN_BCBSM_PRPBooklet_Final122016.pdf

    The actual payoff amount to pediatricians for coercing parents into vaccinating.
    https://community.babycenter.com/post/a63644578/the-actual-payoff-amount-to-pediatricians-for-coercing-parents-into-vaccinating.

    http://thephysicianalliance.org/index.php/incentive-programs

    The Unknown Reasons Doctors Push Vaccines

    Blue Cross, Blue Shield, Blue Care Network of Michigan publishes online a shameless and bold report of how much cash they reward physicians for performing certain tests, and which apparently acts as an incentive to over-prescribe, thus inflating the costs of U.S. healthcare, which should be illegal.

    Blue Cross/Blue Shield published the 2016 Performance Recognition Program, a 28-page report indicating how medical insurance companies actually increase the costs of healthcare!

    Look what we find on the BC/BS page “Childhood Immunizations—Combo 10”!

    If MDs meet a target of 63% of eligible member patients, they will receive a payout of $400 per completed eligible member. Wow! Now you know one of the key reasons why parents are hounded to vaccinate their infants and toddlers. Gelt, pecunia, greenbacks—whatever you call M-O-N-E-Y.

    Read MORE:
    http://www.activistpost.com/2017/08/unknown-reasons-doctors-push-vaccines.html

    TOXIC INGREDIENTS FOUND IN VACCINES: * aluminum hydroxide * aluminum phosphate * ammonium sulfate *amphotericin B * animal tissues: pig blood, horse blood, rabbit brain * dog kidney, monkey kidney * chick embryo, chicken egg, duck egg * calf (bovine) serum * betapropiolactone * fetal bovine serum * formaldehyde * formalin * gelatin * glycerol * human diploid cells (originating from human aborted fetal tissue) * hydrolized gelatin * mercury thimerosol (thimerosal, Merthiolate) * monosodium glutamate (MSG) * neomycin * neomycin sulfate * phenol red indicator * phenoxyethanol (antifreeze) * potassiumdiphosphate * potassium monophosphate * polymyxin B * polysorbate 20 * polysorbate 80 porcine (pig) pancreatic hydrolysate of casein * residual MRC5 proteins * sorbitol * tri(n)butylphosphate * VERO cells, a continuous line of monkey kidney cells * washed sheep red blood plus (source), CDC’s Vaccine Excipients Table:

    DISEASES FROM VACCINES:* Allergies * Asthma * Attention Deficit Disorder *Autism *Auto-immune Diseases * Blindness * Brain Cell Loss *Cancer * Central NervousSystem Damage* Deafness * Developmental Damage *DEATH * Diabetes * Epilepsy *Learning Disabilities * Leukemia * Multiple Sclerosis * Neurological Disease *Organ Disease * Psoriasis * Seizures * Shaken Baby Syndrome * Synergistic Toxicity *SIDS * Total Paralysis *

    https://www.facebook.com/notes/sallie-o-elkordy-for-mayor-vaccine-free-nyc/proposed-executive-order-eo-vaccine-free-2017/1637470476269264/

  • Irregardless of that, the CDC needs to stop ignoring the issue and fund their own studies. But then when did the CDC or FDA ever care about the vaccine truth? They are all right in bed with big pharma.

    Total corruption on every level.

    “Authoritative” Vaccine Medical Information Sources Are Corrupted – December 5, 2017

    “A foolish faith in authority is the worst enemy of the truth” — Albert Einstein The wisdom of this observation is borne out by empirical evidence demonstrating that so-called “authoritative” sources of medical information are thoroughly corrupted not only by industry manipulation but by government officials, and biased, financially conflicted academic gatekeepers of medical science — i.e., “expert panels” and journal editors. The most lucrative areas of medicine are the most corrupted by financial conflicts of interest. Our recent focus continues to be the untouchable subject; namely, the largely corrupted vaccine information base. The history of vaccines has been fashioned by eradicating inconvenient historical facts. The most troubling aspect of the corrupting influence of the powerful vaccine lobby is its apparent success in having averted the focus of the medical profession and academia: from the spiraling number of vaccine-injured children whose existence these authorities deny. However, evidence of their existence is demonstrated by the fraction of those who have been compensated by The U.S. Vaccine Injury Compensation Program (VICP). Public trust in professed authoritative sources for information about vaccine safety has evaporated because the “authoritative” government and non-government agencies have consistently misrepresented the safety data. Internal documents, obtained over the years through FOIA requests, have uncovered the concealed evidence that government officials eliminated damning vaccine safety data from the vaccine information base.

    Read More…
    http://vaccineimpact.com/2017/public-trust-in-professed-authoritative-sources-for-information-about-vaccine-safety-has-evaporated-because-the-authoritative-government-and-non-government-agencies-have-consistently/

    The Vaccine Cartel: Largest Criminal Organization in the World – Why Your Flu Shot is Probably Illegal
    http://vaccineimpact.com/2017/the-vaccine-cartel-largest-criminal-organization-in-the-world-why-your-flu-shot-is-probably-illegal/

    Immunity and Impunity: Corruption in the State‐Pharma Nexus
    Paddy Rawlinson, Western Sydney University, Australia

    Abstract

    Critical criminology repeatedly has drawn attention to the state‐corporate nexus as a site of corruption and other forms of criminality, a scenario exacerbated by the intensification of neoliberalism in areas such as health. The state‐pharmaceutical relationship, which increasingly influences health policy, is no exception. That is especially so when pharmaceutical products such as vaccines, a burgeoning sector of the industry, are mandated in direct violation of the principle of informed consent. Such policies have provoked suspicion and dissent as critics question the integrity of the state‐pharma alliance and its impact on vaccine safety. However, rather than encouraging open debate, draconian modes of governance have been implemented to repress and silence any form of criticism, thereby protecting the activities of the state and the pharmaceutical industry from independent scrutiny. The article examines this relationship in the context of recent legislation in Australia to intensify its mandatory regime around vaccines. It argues that attempts to undermine freedom of speech, and to systematically excoriate those who criticize or dissent from mandatory vaccine programs, function as a corrupting process and, by extension, serve to provoke the notion that corruption does indeed exist within the state‐pharma alliance.

    Conclusion

    If state power is about controlling populations, and corporate power about profit maximization, the vaccine industry feeds both. As such, more than any other area of public health, it demands a respect for human rights, for independent scientific inquiry, and the presence of an effective form of surveillance to ensure that abuses of power are minimized and harms avoided. Indeed, the very premise upon which claims for vaccines is made—that is, their contribution to the betterment of humankind—assumes the presence of these conditions of rights and respect rather than repression and disdain. The editor of The Lancet, Richard Horton, states the obvious, that ‘[i]t would seem within the spirit of scientific inquiry to pose questions that challenge received orthodoxies’ (2015). On this supposition, Edward Jenner, the father of vaccines, was able to pursue what was then regarded as unorthodox, controversial and dangerous thinking. He was afforded the freedom to debate with his peers, to present his findings, to develop his ideas, however contentious they might have been. Whether Jenner’s science was right or wrong is not the issue here. Rather, the fact that he could and did pursue what he genuinely believed would make a contribution to modern medicine is a testament to the spirit of free inquiry that drives scientific advancement. So too, the ability to choose how and when medical intervention can be applied to an individual’s body, without fear of demonisation, is a testament to the spirit of freedom of choice and conscience. When science serves state power, and the state serves the corporate world, each becomes corrupt and corrupting, and society moves one step closer to a repetition of medicine’s darkest time.

    Correspondence: Paddy Rawlinson, Associate Professor in International Criminology, Human and Development Studies, Western Sydney University, Bankstown Campus, Horsley Road and Bullecourt Road, Bankstown 2200 NSW, Australia.

    Just copy and paste this url into your browser, and you will get the full article.

    Read more:
    file:///C:/Users/LH/Downloads/447-1-1931-3-10-20171130.pdf

    Corruption In Big Pharma’s Vaccine Industry
    https://www.naturalblaze.com/2017/12/corruption-big-pharmas-vaccine-industry.html
    http://www.thelibertybeacon.com/corruption-in-big-pharmas-vaccine-industry/

    Attention Parents:
    What Your Doctor Hasn’t Told You About Vaccinations Could Put Your Child at Risk for Autism, Asthma, Allergies, Diabetes or Cancer.
    Get the facts about vaccine risks, before you take any steps to vaccinate your child!
    http://www.immunitionltd.com/ebook/vaccination.htm?hop=activists

  • I don’t have a selective reading comprehension disability, like you do. If you couldn’t lie, simply deny it all, and entirely distort the truth; you would have nothing here at all.

  • All you need to do is consider the below facts, and to realize that that 1 in a million figure is entirely unfounded and based on seriously lacking and flawed data.

    The public as well should consider this information right here in determining the significance of VAERS reports.

    The CDC claim is as well that vaccine injury risk is in the odds of being only 1 in 1 million doses, and then they arrogantly add that even then you likely can not prove it was a vaccine or multiple vaccines. In that being commonly stated there as well seems to be some confusion on it being that ratio number based on individuals vaccinated, or number of vaccine doses generally given in a period of time.That said risk figure is based only on the vaccine injury settlements at the federal vaccine court and as it states in the Data and Statistics page section below. They make a comparison to the number of vaccine doses they estimate to have been given in the time periods that they state.

    Obviously only a fraction of the vaccine injury and resulting death cases are ever filed for with that court, and any more than what we see existing for an estimated on 1 to 10% actual reporting to VAERS in regard to the adverse reactions and resulting deaths in regard to vaccination.

    How many petitions have been awarded compensation?

    According to the CDC, from 2006 to 2015 over 2.8 billion doses of covered vaccines were distributed in the U.S. For petitions filed in this time period, 4,374 petitions were adjudicated by the Court, and of those 2,847 were compensated. This means for every 1 million doses of vaccine that were distributed, 1 individual was compensated.

    Since 1988, over 17,935 petitions have been filed with the VICP. Over that 27- year time period, 16,187 petitions have been adjudicated, with 5,269 of those determined to be compensable, while 10,918 were dismissed. Total compensation paid over the life of the program is approximately $3.6 billion.

    Vaccine Injury Compensation Data
    https://www.hrsa.gov/vaccinecompensation/data/index.html

    As well take a look at the actual VAERS reporting situation!

    February, 2012: The Limits of VAERS

    Underreporting. Because the reports are submitted voluntarily, many patients and doctors do not report vaccine reactions. Different estimates exist for the amount of underreporting and range from a factor of 10 to as much as a factor of 100 (meaning that the true number of vaccine reactions is between 10 and 100 times higher than what is reported to VAERS).

    Read more:
    http://www.medalerts.org/analysis/archives/504

    IS VACCINE INJURY ONE IN A MILLION?!?
    https://www.youtube.com/watch?v=6y09WNx4njY&feature=youtu.be

  • In your world there exists no vaccine truth and nor reality, ever.

    All that exists within your world is the denial of real study science, denial of vaccine injury reality, and as well nothing but refusal to accept anything but the known, and the old and worn out, false vaccine propaganda.

  • Karl Wegner MD

    Well he probably could have helped you but now it’s too late.

  • Karl Wegner MD

    So you don’t want to talk about Wakefield vs Lanka anymore.

  • Karl Wegner MD

    I was trying to update you on the fact that few researchers feel aluminum has anything to do with Alzheimer’s anymore. But you keep right on copy/pasting studies from 40+ years ago Lowell.

  • Karl Wegner MD

    Lowell you don’t have the education to debate medical issues. You think the truth is what you find on anti-vax blogs.

  • Karl Wegner MD

    So you have no idea you just deny it’s less than 1 in a million. Of course.

  • Karl Wegner MD

    Give us your best example of “real study science” then. (you won’t)