Skip to content

Frequency Foundation

Twice the Energy with Half the Stress

Lack of Quality Control in Vaccine Manufacturing

Dirty Vaccines: Every Human Vaccine Tested Was Contaminated With Metals and Debris in New Study – see Int J Vaccines Vaccin 2016, 4(1): 00072

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…

The study explains that these foreign injected impurities may explain a vast array of apparently unrelated adverse events associated with vaccination from headaches and seizures to fatigue, muscle pain, paralysis and sudden infant death syndrome. More likely than not, they speculate, vaccine contaminants will “have a more serious impact on very small organisms like those of children.”

Read more …

Autism and Vaccines Researcher for CDC, Indicted for Fraud and Money-Laundering

Autism continues to radically increase in the U.S. population. Conventional authorities assert that there is no known cause and that there is no link to vaccines. Whenever physicians say there is no known cause for anything it means they are either clueless, lying, or just refusing to investigate for political reasons.
One thing is for sure. Something is causing autism rates to increase. Therefore, it is interesting that a CDC researcher that helped to debunk the vaccine data has been indicted for fraud.

Autism and Vaccines Researcher for CDC, Indicted for Fraud and Money-Laundering
Submitted by Lois Rain on April 22, 2011 – 1:30 pm

Remember when the vaccine mercury/autism link was supposedly debunked? Poul Thorsen, a Danish scientist who coordinated the CDC-funded “debunking” studies, was indicted on April 13th for 13 counts of fraud and 9 counts of money-laundering. Charges relate to his work for the CDC to study correlations between thimerosal (mercury-based vaccine preservative) and the increased rates of autism, among other infant and childhood disabilities he studied. He allegedly stole around $1 million from Atlanta’s CDC autism research money. The fraud charges have to do with dozens of invoices he submitted for “expenses.” The invoices falsely claimed laboratory work from the CDC.

SafeMinds group has closely watched vaccine-autism data brought forth since 2001. Read below about the incongruities they discovered in Thorsen’s work and his emails compelling the CDC to compel the journal Pediatrics to publish his work as a “strong piece of evidence that thimerosal is not linked to autism.” Due to Thorsen’s misconduct, SafeMinds and Coalition for Mercury-Free Drugs are calling for independent federal investigation for data manipulation.

See also Pseudoscience: Most Published Research Cannot be Replicated.

~Health Freedoms

Roundup Connection to Autism

The Warning: A Prediction That Shocked an Audience

In December 2014, Dr. Stephanie Seneff — a Senior Research Scientist at MIT with over 170 peer-reviewed publications — made a declaration that stunned a room of approximately 70 people at a special panel discussion about GMOs.

“At today’s rate, by 2025, one in two children will be autistic.”

The audience, by all accounts, was deeply unsettled. A fellow panelist reported that after Dr. Seneff’s presentation, everyone in attendance “was squirming, likely because they now had serious misgivings about serving their kids, or themselves, anything with corn or soy, which are nearly all genetically modified and thus tainted with Roundup and its glyphosate.”

At the time, this prediction was widely dismissed by mainstream commentators as alarmist. We published this article that same month because the underlying evidence Dr. Seneff presented was too important to ignore.

The Evidence Dr. Seneff Presented

Dr. Seneff’s research focused on the relationship between glyphosate — the active ingredient in Monsanto’s Roundup herbicide — and the rising rates of autism spectrum disorder. Her work over more than three decades spanned biology, technology, nutrition, and health, with particular focus on Alzheimer’s disease, autism, and cardiovascular diseases, as well as the impact of nutritional deficiencies and environmental toxins on human health.

Her key findings included several striking observations. She demonstrated that the side effects of autism closely mimic the symptoms of glyphosate toxicity. Her data showed a remarkably consistent statistical correlation between the increased use of Roundup on crops and the creation of Roundup-ready GMO crop seeds with rising rates of autism diagnosis. She also identified that children with autism carry biomarkers indicative of excessive glyphosate exposure, including zinc and iron deficiency, low serum sulfate, seizures, and mitochondrial disorder.

The mechanism she proposed was straightforward: glyphosate disrupts the gut microbiome, impairs sulfate metabolism, chelates essential minerals, and crosses the blood-brain barrier — creating the exact conditions associated with autism spectrum disorder and other neurodevelopmental conditions.

2025 Update: A Decade Later, the Science Caught Up

We are now past the 2025 date in Dr. Seneff’s prediction. While autism rates have not reached one in two, the trajectory she identified has proven directionally correct — and the scientific establishment has largely validated the concerns she raised about glyphosate neurotoxicity.

The Numbers Have Continued to Rise

When Dr. Seneff made her prediction in 2014, the CDC reported autism prevalence at approximately 1 in 68 children. By 2023, that number had risen to approximately 1 in 36 — nearly doubling in less than a decade. While the one-in-two prediction has not materialized within the specific timeframe, the rate of increase has been dramatic and continues to accelerate.

Glyphosate Neurotoxicity Is No Longer Disputed

In 2014, suggesting that glyphosate was neurotoxic was considered fringe. Today, the picture has changed substantially. The International Agency for Research on Cancer (IARC), a division of the World Health Organization, classified glyphosate as “probably carcinogenic to humans” in 2015 — just one year after this article was published. Bayer (which acquired Monsanto in 2018) has paid over $10 billion in legal settlements related to Roundup health claims. Multiple peer-reviewed studies have now documented glyphosate’s ability to cross the blood-brain barrier, disrupt the gut-brain axis, impair mitochondrial function, and trigger neuroinflammation.

Dr. Seneff herself published a comprehensive book, Toxic Legacy: How the Weedkiller Glyphosate Is Destroying Our Health and the Environment (2021), synthesizing decades of her research into a detailed examination of glyphosate’s mechanisms of harm.

What This Article Got Right in 2014

When the Frequency Research Foundation published this piece in December 2014, we were among the earliest voices highlighting the glyphosate-neurotoxicity connection. The mainstream scientific community took nearly a decade to reach the same conclusions. This pattern — early identification of environmental health threats that are later validated — reflects the foundation’s commitment to following the evidence rather than waiting for consensus.

The Connection to Alzheimer’s Disease

The neurotoxic mechanisms that link glyphosate to autism also implicate it in Alzheimer’s disease. This is not a coincidence. Both conditions involve chronic neuroinflammation, disrupted gut-brain communication, mitochondrial dysfunction, impaired sulfate metabolism, and accumulation of toxic substances in brain tissue.

Dr. Seneff’s own research encompassed Alzheimer’s alongside autism — she recognized that the same environmental toxin was driving neurological damage across the age spectrum. In children, the developing brain is most vulnerable, manifesting as autism. In older adults, the accumulated damage manifests as cognitive decline and Alzheimer’s.

We explore the specific connection between glyphosate and Alzheimer’s risk in our dedicated article Glyphosate Alzheimer’s Disease: Could This Common Herbicide Increase Your Risk?. For the complete picture of how environmental toxins, infections, inflammation, and disrupted brain frequencies all contribute to Alzheimer’s, read our complete guide to Alzheimer’s disease and frequency therapy.

The Aluminum Connection

Glyphosate does not act alone. One of the most concerning aspects of Dr. Seneff’s research is how glyphosate interacts with other environmental toxins — particularly aluminum. As Dr. Dietrich Klinghardt has documented, glyphosate dramatically increases the toxicity of inhaled aluminum nanoparticles. Without glyphosate present in the body, ingested aluminum causes relatively limited damage. But when glyphosate is present — and it is now detectable in the vast majority of the population — even small amounts of inhaled aluminum become highly toxic to brain tissue.

This synergistic toxicity between glyphosate and aluminum creates a compounding threat to neurological health. The aluminum triggers chronic neuroinflammation and parasite infections, while the glyphosate impairs the body’s ability to detoxify and defend itself. Together, they accelerate neurodegeneration.

Our article Geoengineering – Nano Aluminum Creates Chronic Parasite Infections in Populations covers the aluminum side of this equation in detail, including Dr. Klinghardt’s research and the landmark study finding some of the highest aluminum levels ever recorded in human brain tissue.

How Frequency Therapy Addresses Glyphosate Damage

At the Frequency Research Foundation, Dr. Jeff Sutherland has developed frequency protocols that address the multiple layers of damage caused by glyphosate and its interaction with other environmental toxins. This is not a single-target approach. Effective treatment needs to address the full cascade of effects.

Frequency therapy can target the parasite infections that thrive in a glyphosate-compromised system. It can support detoxification pathways for clearing glyphosate, aluminum, and other toxic metals. Targeted frequencies address the chronic neuroinflammation that drives both autism and Alzheimer’s progression. Brain-specific frequencies, including 40 Hz gamma stimulation, support neuronal health and cognitive function.

This multi-target approach is what makes frequency therapy uniquely suited to environmental toxicity cases. Pharmaceutical interventions typically address a single mechanism. Frequency protocols can address multiple contributing factors simultaneously.

Concerned about glyphosate exposure and its neurological effects? Dr. Jeff Sutherland offers personalized paid consultations to assess your situation and develop a targeted frequency protocol. Book Your Consultation

Frequently Asked Questions

Take the Next Step

The evidence connecting Roundup’s glyphosate to neurological damage in both children and adults is now too strong to ignore. If you are concerned about environmental toxin exposure — whether for yourself, your children, or an aging parent — a consultation with Dr. Jeff Sutherland can help you understand the full picture and develop a personalized frequency protocol.

Book Your Consultation with Dr. Jeff Sutherland

This article is part of our comprehensive Alzheimer’s resource library. Glyphosate is one of several environmental risk factors for Alzheimer’s disease. Read our complete guide to Alzheimer’s disease and frequency therapy for the full scope of research, nutritional strategies, and frequency-based treatment approaches.

© Frequency Research Foundation. This content is for educational and informational purposes only. It is not intended to diagnose, treat, cure, or prevent any disease. Always consult with qualified healthcare professionals regarding medical conditions.

MMR Vaccine Increases Autism in Blacks by over 300%

Measles-mumps-rubella vaccination timing and autism among young african american boys: a reanalysis of CDC data

Brian S Hooker




Translational Neurodegeneration 2014, 3:16  doi:10.1186/2047-9158-3-16

Published: 8 August 2014

Background

A significant number of children diagnosed with autism spectrum disorder suffer a loss of previously-acquired skills, suggesting neurodegeneration or a type of progressive encephalopathy with an etiological basis occurring after birth. The purpose of this study is to investigate the effectof the age at which children got their first Measles-Mumps-Rubella (MMR) vaccine on autism incidence. This is a reanalysis of the data set, obtained from the U.S. Centers for Disease Control and Protection (CDC), used for the Destefano et al. 2004 publication on the timing of the first MMR vaccine and autism diagnoses.

Methods

The author embarked on the present study to evaluate whether a relationship exists between child age when the first MMR vaccine was administered among cases diagnosed with autism and controls born between 1986 through 1993 among school children in metropolitan Atlanta. The Pearson’s chi-squared method was used to assess relative risks of receiving an autism diagnosis within the total cohort as well as among different race and gender categories.

Results

When comparing cases and controls receiving their first MMR vaccine before and after 36 months of age, there was a statistically significant increase in autism cases specifically among African American males who received the first MMR prior to 36 months of age. Relative risks for males in general and African American males were 1.69 (p=0.0138) and 3.36 (p=0.0019), respectively. Additionally, African American males showed an odds ratio of 1.73 (p=0.0200) for autism cases in children receiving their first MMR vaccine prior to 24 months of age versus 24 months of age and thereafter.

Conclusions

The present study provides new epidemiologic evidence showing that African American males receiving the MMR vaccine prior to 24 months of age or 36 months of age are more likely to receive an autism diagnosis.
Keywords: 

Autism; Measles-mumps-rubella (MMR) vaccine

Genetic Risk Factors for Autism

Patrick Bolton and Hilgo Bruining on connecting genetic risk factors to specific symptoms in autism

Posted by Biome on 24th February 2014 –  0 Comments

Genome wide association studies, genetic epidemiological investigations and numerous gene sequencing approaches have led to a growing appreciation of a genetic component to autism spectrum disorder (ASD). Genetic variations have consequently been linked to a broad spectrum of behavioural symptoms that fall within the classification of ASD. However, for the large part, these risk factors have not been correlated with specific symptomatology. Such a correlation might be important to dissect the heterogeneity of ASD, which is urgently needed to develop more targeted treatment possibilities. In a recent study in Molecular Autism, Patrick Bolton from King’s College London, UK, Hilgo Bruining from the Brain Centre Rudolf Magnus, the Netherlands, and colleagues, investigate the genetics of ASD with a view to determining whether specific behavioural signatures can indeed be linked to certain genetic traits. Bolton and Bruining explain how they were able to discern behavioural symptoms unique to specific genetic disorders that are known to carry an increased risk for ASD, and moreover discuss how this machine-learning approach could be applied to idiopathic ASD.
——
Frequency Research Foundation has reported previously that about half the population has mercury, flouride, and measles virus in the brain along with other viruses and heavy metals. See:

http://blog.frequencyfoundation.com/2006/05/evidence-of-harm-mercury-in-vaccines.html

However, only a subset of these people are autistic and they have particular problems with the measles virus in the intestinal tract along with heavy concentrations of mercury in the brain. This suggests genetic factors that disrupt the elimination of mercury and make the intestinal tract susceptible to the measles virus. Thus this latest research is of interest because it shows a genetic predisposition to autism.

Autism: Related to Abnormalities in Gut Bacteria

Reduced Incidence of Prevotella and Other Fermenters in Intestinal Microflora of Autistic Children

  • Dae-Wook Kang equal contributor,

    •  

  • Jin Gyoon Park equal contributor,

    •  

  • Zehra Esra Ilhan,

    •  

  • Garrick Wallstrom,

    •  

  • Joshua LaBaer,

    •  

  • James B. Adams,

    •  

  • Rosa Krajmalnik-Brown mail

Abstract

High proportions of autistic children suffer from gastrointestinal (GI) disorders, implying a link between autism and abnormalities in gut microbial functions. Increasing evidence from recent high-throughput sequencing analyses indicates that disturbances in composition and diversity of gut microbiome are associated with various disease conditions. However, microbiome-level studies on autism are limited and mostly focused on pathogenic bacteria. Therefore, here we aimed to define systemic changes in gut microbiome associated with autism and autism-related GI problems. We recruited 20 neurotypical and 20 autistic children accompanied by a survey of both autistic severity and GI symptoms. By pyrosequencing the V2/V3 regions in bacterial 16S rDNA from fecal DNA samples, we compared gut microbiomes of GI symptom-free neurotypical children with those of autistic children mostly presenting GI symptoms. Unexpectedly, the presence of autistic symptoms, rather than the severity of GI symptoms, was associated with less diverse gut microbiomes. Further, rigorous statistical tests with multiple testing corrections showed significantly lower abundances of the genera Prevotella,Coprococcus, and unclassified Veillonellaceae in autistic samples. These are intriguingly versatile carbohydrate-degrading and/or fermenting bacteria, suggesting a potential influence of unusual diet patterns observed in autistic children. However, multivariate analyses showed that autism-related changes in both overall diversity and individual genus abundances were correlated with the presence of autistic symptoms but not with their diet patterns. Taken together, autism and accompanying GI symptoms were characterized by distinct and less diverse gut microbial compositions with lower levels of Prevotella, Coprococcus, and unclassified Veillonellaceae.
Citation: Kang D-W, Park JG, Ilhan ZE, Wallstrom G, LaBaer J, et al. (2013) Reduced Incidence of Prevotella and Other Fermenters in Intestinal Microflora of Autistic Children. PLoS ONE 8(7): e68322. doi:10.1371/journal.pone.0068322

Mercury and Autism: The Smoking Gun

 2012;72(2):113-53.

Evidence of parallels between mercury intoxication and the brain pathology in autism.

Source

Institute of Chronic Illnesses, Inc., Silver Spring, MD, USA. jkern@dfwair.net

Abstract

The purpose of this review is to examine the parallels between the effects mercury intoxication on the brain and the brain pathology found in autism spectrum disorder (ASD). This review finds evidence of many parallels between the two, including: (1) microtubule degeneration, specifically large, long-range axon degeneration with subsequent abortive axonal sprouting (short, thin axons); (2) dentritic overgrowth; (3) neuroinflammation; (4) microglial/astrocytic activation; (5) brain immune response activation; (6) elevated glial fibrillary acidic protein; (7) oxidative stress and lipid peroxidation; (8) decreased reduced glutathione levels and elevated oxidized glutathione; (9) mitochondrial dysfunction; (10) disruption in calcium homeostasis and signaling; (11) inhibition of glutamic acid decarboxylase (GAD) activity; (12) disruption of GABAergic and glutamatergic homeostasis; (13) inhibition of IGF-1 and methionine synthase activity; (14) impairment in methylation; (15) vascular endothelial cell dysfunction and pathological changes of the blood vessels; (16) decreased cerebral/cerebellar blood flow; (17) increased amyloid precursor protein; (18) loss of granule and Purkinje neurons in the cerebellum; (19) increased pro-inflammatory cytokine levels in the brain (TNF-α, IFN-γ, IL-1β, IL-8); and (20) aberrant nuclear factor kappa-light-chain-enhancer of activated B cells (NF-kappaB). This review also discusses the ability of mercury to potentiate and work synergistically with other toxins and pathogens in a way that may contribute to the brain pathology in ASD. The evidence suggests that mercury may be either causal or contributory in the brain pathology in ASD, possibly working synergistically with other toxic compounds or pathogens to produce the brain pathology observed in those diagnosed with an ASD.

Vaccine Related Research: Thimerosal Alters Brain Function

 2012 Jun;63(3):277-83.

Sex-dependent changes in cerebellar thyroid hormone-dependent gene expression following perinatal exposure to thimerosal in rats.

Source

Department of Psychiatry, Harvard Medical School/BWH, Boston, MA 02115, USA.

Abstract

Mammalian brain development is regulated by the action of thyroid hormone (TH) on target genes. We have previously shown that the perinatal exposure to thimerosal (TM, metabolized to ethylmercury) exerts neurotoxic effects on the developing cerebellum and is associated with a decrease in cerebellar D2 activity, which could result in local brain T3 deficiency. We have also begun to examine TM effect on gene expression. The objective of this study was to expand on our initial observation of altered cerebellar gene expression following perinatal TM exposure and to examine additional genes that include both TH-dependent as well as other genes critical for cerebellar development in male and female neonates exposed perinatally (G10-G15 and P5 to P10) to TM. We report here for the first time that expression of suppressor-of-white-apricot-1 (SWAP-1), a gene negatively regulated by T3, was increased in TM-exposed males (61.1% increase), but not in females; (p<0.05). Positively regulated T3-target genes, Purkinje cell protein 2 (Pcp2; p=0.07) and Forkhead box protein P4 (FoxP4; p=0.08), showed a trend towards decreased expression in TM-exposed males. The expression of deiodinase 2 (DIO2) showed a trend towards an increase in TM-exposed females, while deiodinase 3 (DIO3), transthyretin (TTR), brain derived neurotrophic factor (BDNF) and reelin (RELN) was not significantly altered in either sex. Since regulation of gene splicing is vital to neuronal proliferation and differentiation, altered expression of SWAP-1 may exert wide ranging effects on multiple genes involved in the regulation of cerebellar development. We have previously identified activation of another TH-dependent gene, outer dense fiber of sperm tails 4, in the TM exposed male pups. Together, these results also show sex-dependent differences between the toxic impacts of TM in males and females. Interestingly, the genes that were activated by TM are negatively regulated by TH, supporting our hypothesis of local brain hypothyroidism being induced by TM and suggesting a novel mechanism of action TM in the developing brain.

Frequency Update: Measles Vaccine Complex 2.0

The latest research shows that polyomavirus is associated with autism. Frequency Foundation has determined the frequency set for this virus and added it to the measles vaccine series. About 50% of the people I test appear to benefit from the measles vaccine frequency set so they are made available to other researchers for further testing.

Substantial updates to viral frequency and the frequency for mercury have been included in this version. The frequency program developed for multiple types of Rife devices includes:

*frequencies for polyomavirus
*frequencies that help eliminate mercury, aluminum, and fluoride
*measles virus frequency set
*frequencies for helping to eliminate fatty deposits in the brain
*frequency for stimulating hypothalamus function
*a second virus frequency set that always appears with measles virus
*multiple strains of candida and other fungi
*multiple parasite strains
*multiple bacterial infections

These multiple organisms appear in every case tested, i.e. they always occur together, and with a specific focus in the hypothalamus which leads to inability to process external stimuli properly. This affects internal perception of the world and causes a negative effect on interpersonal relations. Chronic infection of the hypothalamus with an aging immune system may cause more serious complications. Therefore, these organisms should all be eliminated as soon as possible.
—–
Time Magazine reported on Autism recently. See “Inside the Autistic Mind” by Claudia Wallis, 15 May 2005. While this may be worth reading, you will get a lot more useful information from the New York Times:

Morrice, Polly. Evidence of Harm: What Causes the Autism Epidemic. New York Times, 17 Apr 2005.

Kirby, David. Evidence of Harm. New York Times, 17 Apr 2005. (First chapter of book)

Read David Kirby’s book. It’s enlightening!

Kirby, David. Evidence of Harm – Mercury in Vaccines and the Autism Epidemic: A Medical Controvery. St. Martins Griffin, 2005

Here, we can do some original research by doing Photo Analysis on the Time cover, assuming the boy is autistic. What does he have in his brain, particularly the hypothalamus? Visiting a physician colleague this week, I learned that his patients who look right through you and appear not to be home have a malfunctioning hypothalamus which he can easily fix in most cases.

The first thing I pick up is a parasite infection. Looks like one of the Lyme parasites he probably picked up from his dog. More important, he clearly has the measles virus in his brain and his gut. Autistic kids usually have serious intestinal problems.

Pulling out Netter’s Atlas of Human Anatomy and focusing on the brain, I find mercury and the measles virus located particularly in the hypothalamus. In addition, I find aluminum there. Kirby has documented the synergistic relationship between mercury and aluminum which allows the two together to kill far more neurons.

Since autistic children have altered physical structures in the brain, I looked for aberrant cells and found a frequency for fatty deposits. Finally, I identified the frequency for physically stimulating the hypothalamus.

Testing other people for this condition, I find that many people have the same problem in the hypothalamus. Mercury and aluminum evidently migrate to that area of the brain. Many people also have the measles virus in the hypothalamus, but not in the gut. Apparently, everyone that gets the vaccine has this problem, but not everyone is noticeably autistic.

Testing myself, I find the same contaminants in the hypothalamus. After developing an F165 program as a solution, I transmit the frequencies using one of my ABPA devices and find it has a soothing, relaxing, mellowing effect. The next morning I find it a little easier to focus, stimuli are less disturbing as I wake up, and I feel more comfortable with intimacy. Evidently, many of us are just a little bit autistic.

It should be noted that males, for genetic reasons, are far more susceptible to effects of this contamination than females, even though females also have mercury, aluminum, and measles in the hypothalamus. No wonder the women are complaining about the men all the time!

Running these frequencies stimulates the immune system and flushes out another virus, a strain of candida, two strains of babesia, and a bacteria. These do not seem to be present in the boy on the cover of Time. However, they seem to all be present across a group of adults that I have tested. This is yet another example of how compromising the immune system can lead to increasing negative effects with aging and associated exposure to other pathogens.

So autism looks like it is a combination of the mercury killing neurons and lowering immune function, in combination with other vaccine contaminants. This allows the measles virus to create a chronic infection. Those diagnosed with autism are genetically unable to eliminate mercury effectively, have higher mercury levels, and the virus chronically infects the gut and starts an autoimmune reaction. The hypothalamus is particularly infected.