21 September 2016

Black Mold and Other Mold Frequencies Release 4.1

Staying in a mold filled apartment in Europe motivated an upgrade to mold frequencies, particularly Chaetomium. Also a third file is added with toxin frequencies commonly seen in mold and lyme infections.

Rereading Scott Forsgren's article on Mold and Mycotoxins reminded me that hundreds of updates to mold frequencies have been identified since my previous update.

Everyone runs into mold on a regular basis and these frequencies can help tremendously. I've included every mold that my clients have encountered during the last 20 years. If you find a new one (unlikely) please send me an email. Subscribers feel free to send me an email if you need help in identifying mold frequencies.

A previous release included mold commonly found in coffee which most of you are exposed to. An easy trick to determine if you have mold in the air in your home is to leave a little milk out in a glass overnight. If there is mold in the air, it will start growing in the milk. I use a Nespresso Aerochino which warms and froths the milk. Left unattended overnight with remains of frothed milk, it provides an optimal growth environment for mold.

When I awake in the morning I can see if there is mold easily in the Aerochino. I then test with the Cameron Aurameter to determine the frequency. The primary frequency for molds is in the 400khz range.  I then search the file below for the right frequency set.

Note: Candida is a fungus as well and found in a separate program on the subscribers site.

27 July 2016

Parasites: Opening Up a Massive Frequency Database

There are thousands of parasites and everyone is infected with hundreds of them. They are the major transmission route for flu, involved in all cancers, and carry with them other viruses, bacteria, fungi, mycoplasma, and other pathogens and toxins. Malaria, giardia and rosacea are just a few of the hundreds of medical conditions caused by parasites.

Only a few parasites can be identified by lab tests and then usually only in the stool in one out of five samples. Even when identified, conventional medicine offers only toxic medications which are often ineffective.

Parasites are easily eliminated from the body within a few hours with the correct frequencies. Each parasite strain requires multiple frequencies to knock out each stage of the life cycle plus frequencies to knock out critical proteins.

The complexity of multiple frequencies and multiple strains makes it difficult for most researchers to systematically eliminate parasites. Frequency Foundation has spent more than two decades of research to be able to do this consistently and effectively with frequencies only.

Our database has evolved to many thousands of parasite strains, each with up to 30 frequencies to eliminate them. Frequency Research Foundation subscribers requested that they be posted online so they can do database searches for specific frequencies which are useful. Over the next few months, the entire research database on parasites will be made available to subscribers.

Parasite immunomodulation and polymorphisms of the immune system

Rick M Maizels 
Centre for Immunity, Infection and Evolution, and Institute of Immunology and Infection Research, University of Edinburgh, Edinburgh, EH9 3JT, UK
Journal of Biology 2009, 8:62doi:10.1186/jbiol166
The electronic version of this article is the complete one and can be found online at: http://jbiol.com/content/8/7/62
Published: 5 August 2009
© 2009 BioMed Central Ltd


Parasites are accomplished evaders of host immunity. Their evasion strategies have shaped every facet of the immune system, driving diversity within gene families and immune gene polymorphisms within populations. New studies published recently in BMC Biology and Journal of Experimental Medicine document parasite-associated immunosuppression in natural populations and suggest that host genetic variants favoring resistance to parasites may be detrimental in the absence of infection.


Parasites are eukaryotic pathogens, and broadly comprise protozoa, fungi, helminths and arthropods (Figure 1) that complete part or all of their life cycle within a host organism. Like other pathogens, parasites must survive in the face of a highly potent immune system. They succeed in this through a great diversity of strategies for avoiding immune detection, suppressing cellular immunity and deflecting immune attack mechanisms. It has been suggested that the need to overcome suppressive mechanisms of parasites may have led to compensatory adjustments in immune genes that, in an environment where parasitic infection is not endemic, may increase the likelihood of inappropriate responsiveness to self-antigens (autoimmunity) and environmental allergens (allergy). This notion has become known as the hygiene hypothesis [1]. Two recent papers, from Jackson et al. [2] and Fumagalli et al. [3] lend support to this hypothesis.

24 July 2016

Frequency Research Lab Setup - SG1, DMI, SG8 Amp, Harmony Evolution Chip

Researchers, test your sytems!

We have gone through our lab setups and incorporated the latest findings for setting up DMI boards on top of SG1 transmitters. This has resulted in a much more effective laboratory for frequency research. Systems need to be oriented towards magnetic north to get best results.

The standard Frequency Research Lab setup based on two decades of frequency research is easily affordable for computer users and includes:

1. Computer - PC or Mac
2. F165 frequency generator
3. SG1 transmitter
4. DMI board for digital photos
5. Harmony Evolution Chip to create more effective frequencies

The photo above shows a DMI board properly placed on an SG1 transmitter. Our lab systems have SG8 amplifiers so that we can run up to 8 SG1s with one F165 frequency generator.

The PDF in the link below shows exactly how to place a DMI on top of an SG1. Geometry is critical. The wrong angle or positioning will result in no effective frequency transmission!

The PDF also shows how to insert a Harmony Evolution Chip under the DMI for maximum response. Some trolls on the internet have complained that the Harmony Chip is useless. I make no claims for the Harmony Chip except to state that my testing shows my lab setup is about 10 times as effective as a lab without the chip.

Do your own testing!

If you have an SG8 amp, you can power up to 8 SG1s from a single frequency generator. In this case, you need only one Harmony Chip placed on the SG8 to affect up to 8 SG1 transmissions.

If you need assistance with equipment or setup up contact info@frequencyfoundation.com and we will connect you with Longevity Research, LLC. They sell all our equipment. Frequency Research Foundation does not sell any equipment, only frequency data for use with recommended equipment. This allows us to be impartial about what equipment to use. We are only interested in what works the best given currently available hardware.

Click here for PDF on how to setup your lab properly...

17 July 2016

Fluoride Supplements Banned by the FDA?

On January 13, 2016, the FDA issued a Warning Letter to a pharmaceutical company (Kirkman Industries, Inc.), ordering the company to "discontinue marketing all of the unapproved prescription drugs manufactured at [the] facility immediately.” The unapproved prescription drugs that FDA identified were fluoride "supplements."

Fluoride supplements are sodium fluoride containing drops, tablets, and lozenges that are sold for the purpose of preventing tooth decay. FDA's Warning Letter makes clear that marketing fluoride supplements as cavity preventatives violates federal law because the FDA has never approved fluoride supplements as safe and effective for this purpose. Read more ...

04 July 2016

Biofilms Version 6.0 - thousands of updates

Biofilm Version 6.0 is the first upgrade in six months. Thousands of updates and many more bacterial strains have been made to biofilm frequencies in this release. Always use the latest frequencies, particularly for biofilms, in order to minimize herx responses.

Most of the 600 strains of periodontal biofilms DNA sequenced by the National Institutes of Health are now  in this series of programs. Most strains of lyme disease borrelia are included. Nanobacteria and other biofilms associated with Altzheimers can be found here. Biofilms are associated with all major disease categories. There is even a new program targets abdominal fat.

Recent research has focused on biofilm involvement in tumors. All tumors (benign and malignant) are infected with biofilms. The relationship of causation of tumors by biofilms is still being researched. It appears that many so-called Rife frequencies are really components of biofilms.

There is extensive academic research on biofilms. See Montana State University Center for Biofilm Engineering for the basics, as well as access to papers from dozens of conferences. For example, most people have biofilms forming calcification in their joints and articles. Here is a photo of such a biofilm on a grain of sand:

These biofioms are not doing your heart any good.

Most bacteria infections today are antibiotic resistant biofilms. While over 600 species of these biofilms have been DNA sequenced for periodontal disease, these gum infections are the tip of the iceberg. A huge amount of illness from joint problems to wound infections to heart disease are caused by biofilms.

During the past two years, intensive research at the Frequency Research Foundation has developed frequency sequences for about 400 biofilms. A notable finding is that radical reduction in blood pressure can be achieved by running the appropriate borrelia biofilm programs for infected individuals. All people exposed to lyme disease will need them.

January 2005, National Institute of Dental and Craniofacial Research
It has long been assumed that all chronic periodontitis is the same no matter where one lives in the world.  But some scientists have wondered whether the bacterial composition of the oral biofilm - the sticky, mat-like microbial communities that form on our teeth and cause chronic periodontitis - might vary geographically.  In the November issue of the Journal of Clinical Periodontology, NIDCR grantees and their colleagues report for the first time that this is indeed the case.  In a study of more than 300 patients with chronic periodontitis from Sweden, the United States, Brazil, and Chile, they found clear geographical differences in the bacterial content of dental plaque obtained from the periodontal lesions.  To hear more about this important paper, the Inside Scoop recently talked with lead author Anne Haffajee, B.D.S., and Sigmund Socransky, D.D.S., the senior author. Both are scientists at The Forsyth Institute in Boston.

Work on biofilms is becoming as extensive as previous work on lyme disease frequencies. Daily updates indicate that they are at the root of much of heart disease, respiratory problems, joint issues, prostate problems, and tumors of all types. Recent releases added many biofilms seen with abnormal cells in cancer patients, raising the question as to whether they are involved in carcinogenesis.
There are over 600 species of periodontal biofilms that have been DNA sequenced. During the past two years, the Frequency Research Foundation has expanded detailed analysis of  frequencies for many more biofilm infections. This is the most extensive research effort since development of the lyme disease frequency sets and has involved daily analysis and update of biofilm frequencies from September 2011 until July 2013. As a result these data are the most comprehensive biofilm frequency sets available.

Some are based on the lyme borellia spirochete and cause elevated blood pressure. Others are directly related to mortality from heart disease.

Persistent Chlamydia pneumoniae infection of cardiomyocytes is correlated with fatal myocardial infarction.
Spagnoli LG, Pucci S, Bonanno E, Cassone A, Sesti F, Ciervo A, Mauriello A.

All biofilms can go systemic in the body and cause a wide variety of symptoms and disease outcomes. For the first time it is possible to work on getting rid of the root cause of gum disease and other persistent infections. 
Frequencies are published as a set of over a dozen F165 program files. It is best to work on one biofilm frequency set at a time as one clinician has noted that use of these frequencies is analogous to tearing up the floorboards in your house. You never know what you are going to find underneath.

Biofilm frequencies are available to subscribers.

26 June 2016

Mosquitos and the West Nile Virus Version 3.0

Madeline Drexler does a fascinating piece of work in her book, Secret Agents, on the outbreak of the West Nile Virus in New York in 1999 where it tooks weeks to find out what virus was killing birds and people. Finally, on 22 September 1999, a CDC scientist loaded samples of the virus genome into a machine that automatically sequenced the DNA strands. The next morning, he submitted strings of genetic code over the internet to the National Library of Medicine GenBank and got a hit on the West Nile Virus.

Frequencies of pathogens are related to DNA. It is a lot faster and easier to determine a frequency sequence and then search gigabytes of data in the Frequency Research Foundation database than it is to spend weeks trying to culture a virus. A pathogen can often be identified within a few minutes.

After returning from long European trip in June 2016, I woke up at night with a pain in my chest. Testing for frequencies, then scanning the database, showed I was infected with the West Nile Virus. I then tested my dog who was sleeping with me and he had obviously picked up the virus in the Massachusetts woods while I was away.

Frequencies for several strains of West Nile Virus needed to be run to clear up the dog and me. All strains with their latest updates are posted on the Frequency Foundation subscribers site.

In addition, frequencies were transmitted to eliminate mosquitos from the woods where he stayed while I was gone using the Frequency Foundation mosquito service which requires only a small fee per month.

Mosquitos transmit many pathogens that have been found in my area:

  • Lyme disease
  • Zika virus
  • West Nile Virus
  • etc.

A few years ago my wife picked up a shingles infection from a mosquito bite on a houseboat in Amsterdam. I was bitten by many malaria infested mosquitos in India earlier this year. Getting rid of the mosquitos is a lot less painful than dealing with the infections.

Our research shows that every mosquito species transmits a signature pathogen into the human body and targeting that organism in the mosquito causes the mosquito to die. Our database has frequencies for hundreds of species of mosquitos, ticks, and flies gathered over the last decade with the help of many clients and fellow researchers.

Apparently, once you are infected with a mosquito's signature pathogen it stays there for life unless removed with frequencies. Then you become a tender morsel for mosquitos with that frequency sequence. This explains why mosquitos love specific individuals. 

USGS CDC West Nile Virus 8 Aug 2014

While there is only animal West Nile Virus activity reported in Massachusetts, a client picked up a strain in Whole Foods in 2014 so there are unreported human cases. West Nile is a nasty virus so it is good to have updated frequencies on hand.

Mosquito's transmitting West Nile Virus can be found all over the United States. This virus has been part of the lyme series since 2005 and was an important component of the swine flu which distributed it everywhere. 

According to the Mayo Clinic, humans can become infected with West Nile after being bitten by an infected mosquito.  Mosquitoes contract the virus when they feed on infected birds. While there have been no reported human cases yet, officials recommend taking the necessary precautions to prevent the virus – such as using insect repellent outdoors, especially from dusk until dawn, and wearing long pants and long sleeved shirts.

People should also make sure their door and window screens are not broken, health officials said; and to stop mosquitoes from breeding, they should empty any standing water that might have collected in garden pots, pools or trash. 

Frequency Research Foundation Mosquito Research Program

For the past decade fellow researchers have worked with the Frequency Research Foundation to identify frequencies that will make over 150 species of mosquitos go away, including those mosquitos carrying the West Nile Virus.

Specific areas can be targeted for a small monthly fee. Contact info@frequencyresearch.com

Previous West Nile Virus Experience

A client fell down three times in one week incurring some serious scrapes and brushes. Photoanalysis showed she had mosquito frequencies. The specific species of mosquito was targeted for removal of material injected by the mosquito and removal of the mosquito species from the area around her home.

A hadoscan showed low energy spots in her body from the mosquito frequencies and particularly along her spine. West Nile Virus can become a neurological infection which would explain the falling episodes.

Following application of the mosquito frequencies, an unidentified virus in the Lyme program set was discovered. Suspecting that this might be West Nile Virus, an electron microscope photo of the virus was analysed. An exact match was confirmed.

Another client thought he was dying. Application of these frequencies for 12 hours brought him back to normal.

25 June 2016

Post Polio Syndrome Version 3.0

The latest version of Post Polio Syndrome includes many new viruses and hundreds of updates. Always use the latest frequencies for best results.

If you find yourself tripping when going up stairs, checking for one of the viruses in this set might help. These, among many other pathogens, can be found circulating on airplane flights or in airports. Probably the most effective health measure on the planet right now would be to put ozone lights in airport and aircraft air circulation systems as Tesla has done in automobiles.

Recent research has surfaced several additional strains of polio virus circulating with the swine flu. These have been broken out into a separate program and those strains commonly found with lyme disease have been incorporated. All these viruses are found in those with post polio syndrome as well as in many people without obvious clinical symptoms.

The lyme complex has hundreds of viruses including organisms like polio virus. The virus is latent in individuals exposed to polio, even though they may have been vaccinated several times so researchers should check for the present of this virus, particularly if they have been exposed to lyme.


Electron micrograph of poliovirus.
The primary determinant of infection for any virus is its ability to enter a cell and produce additional infectious particles. The presence of CD155 is thought to define the animals and tissues that can be infected by poliovirus. CD155 is found (outside of laboratories) only on the cells of humans, higher primates, and Old World monkeys. Poliovirus is however strictly a human pathogen, and does not naturally infect any other species (although chimpanzees and Old World monkeys can be experimentally infected).[31]
Poliovirus is an enterovirus. Infection occurs via the fecal-oral route, meaning that one ingests the virus and viral replicaion occurs in the alimentary tract.[32] Virus is shed in the feces of infected individuals. In 95% of cases only a primary, transient presence of viremia (virus in the bloodstream) occurs, and the poliovirus infection is asymptomatic. In about 5% of cases, the virus spreads and replicates in other sites such as brown fatreticuloendothelialtissue, and muscle. The sustained viral replication causes secondary viremia and leads to the development of minor symptoms such as fever, headache and sore throat.[33] Paralytic poliomyelitis occurs in less than 1% of poliovirus infections. Paralytic disease occurs when the virus enters the central nervous system (CNS) and replicates in motor neurons within the spinal cordbrain stem, or motor cortex, resulting in the selective destruction of motor neurons leading to temporary or permanent paralysis. In rare cases, paralytic poliomyelitis leads to respiratory arrest and death. In cases of paralytic disease, muscle pain and spasms are frequently observed prior to onset of weakness and paralysis. Paralysis typically persists anywhere from days to weeks prior to recovery.[34][35]
In many respects the neurological phase of infection is thought to be an accidental diversion of the normal gastrointestinal infection.[15] The mechanisms by which poliovirus enters the CNS are poorly understood. Three non-mutually exclusive hypotheses have been suggested to explain its entry. All theories require primary viremia. The first hypothesis predicts that virions passes directly from the blood into the central nervous system by crossing the blood brain barrier independent of CD155.[36] A second hypothesis suggests that the virions are transported from peripheral tissues that have been bathed in the viremic blood, for example muscle tissue, to the spinal cord through nerve pathways via retrograde axonal transport.[37][38][39] A third hypothesis is that the virus is imported into the CNS via infected monocytes or macrophages.[8]
Poliomyelitis is a disease of the central nervous system. However, CD155 is believed to be present on the surface of most or all human cells. Therefore receptor expression does not explain why poliovirus preferentially infects certain tissues. This suggests that tissue tropism is determined after cellular infection. Recent work has suggested that the type I interferon response (specifically that of interferon alpha and beta) is an important factor that defines which types of cells support poliovirus replication.[40] In mice expressing CD155 (through genetic engineering) but lacking the type I interferon receptor, poliovirus not only replicates in an expanded repertoire of tissue types, but these mice are also able to be infected orally with the virus.[41]

This frequency set is available on the Frequency Foundation subscribers blog.

15 May 2016

Nativis: Frequency Medicine Clinical Trial

Nativis science and technology is based on magnetically induced electron and charge transfer. Electron transfer is central to the function of many biologic processes and artificial magnetic fields are capable of triggering a receptor response and conformational change in the absence of a physical agonist. A specific and precise oscillating magnetic field with the proper vector, magnitude and pulse duration can move a charge along a protein pathway much the same way an electron is forced to move in copper wire. A charge moving between a donor and acceptor site in the presence of an oscillating magnetic field will result in a conformational dynamic similar to a naturally forced charge.

Non-Thermal Radio Frequency Stimulation of Tubulin Polymerization in Vitro: A Potential Therapy for Cancer Treatment
John T. Butters1, Xavier A. Figueroa2*, Bennett Michael Butters1 1 Nativis Inc., Seattle, WA, USA 2 Sciencia Incognita Consulting, LLC, Seattle, WA, USA

Copyright © 2014 by authors and Scientific Research Publishing Inc. This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/

Abstract The use of radio frequency energy is an established technology for certain oncology therapies. Direct inputs of radio frequency (RF) energy as thermal energy are applied to ablate tumors or catalyze secondary reactions in adjunct treatments against certain tumor types. Yet, other applications are being developed which take advantage of properties of RFs that impinge on biological proteins and cells without thermal effects. Here we report a proof-of-concept application of specific, digitally encoded, low power (non-thermal) radio frequency energy in an in vitro preparation of a tubulin polymerization assay. The radio frequency energy signal, designated M2(3), was applied to the tubulin polymerization assay samples during spectrophotometric measurements to assess the effectiveness for enhancing tubulin polymerization. A commercially available taxane (paclitaxel) that promotes tubulin polymerization was used as a control to assess the effectiveness of the M2(3) radio frequency energy signal on tubulin polymerization rates. A low power, specific, digital radio frequency energy signal is capable of promoting tubulin polymerization as effectively as a commercially available taxane.

13 April 2016

Pseudoscience: Flouride is Good for You!

The Lancet Neurology

Neurobehavioural effects of developmental toxicity Dr Philippe Grandjean, MDcorrespondenceemail, Philip J Landrigan, MD
Published Online: 14 February 2014


Neurodevelopmental disabilities, including autism, attention-deficit hyperactivity disorder, dyslexia, and other cognitive impairments, affect millions of children worldwide, and some diagnoses seem to be increasing in frequency. Industrial chemicals that injure the developing brain are among the known causes for this rise in prevalence. In 2006, we did a systematic review and identified five industrial chemicals as developmental neurotoxicants: lead, methylmercury, polychlorinated biphenyls, arsenic, and toluene. Since 2006, epidemiological studies have documented six additional developmental neurotoxicants—manganese, fluoride, chlorpyrifos, dichlorodiphenyltrichloroethane, tetrachloroethylene, and the polybrominated diphenyl ethers. We postulate that even more neurotoxicants remain undiscovered. To control the pandemic of developmental neurotoxicity, we propose a global prevention strategy. Untested chemicals should not be presumed to be safe to brain development, and chemicals in existing use and all new chemicals must therefore be tested for developmental neurotoxicity. To coordinate these efforts and to accelerate translation of science into prevention, we propose the urgent formation of a new international clearinghouse.

23 February 2016

Novocure.com - Fast Company #1 Innovator in Biotech

Mechanism of Action

Tumor Treating Fields, or TTFields, are low intensity, alternating electric fields within the intermediate frequency range. TTFields disrupt cell division through physical interactions with key molecules during mitosis. This non-invasive treatment targets solid tumors.

The beginning of mainstream electronic medicine. Novocure makes Fast Company top innovator list!

20 February 2016

Nanobacteria Version 2.0 - always use with chelation

Research on nanobacteria has evolved over the last decade. After developing complex frequency sequences for hundreds of biofilms, a number of them are nanobacteria that increase diastolic blood pressure and are directly related to heart disease.

For the first time in over a decade I am publishing frequencies for dozens of the most common nanobacteria strains. Those with the capability of determining what frequencies are needed will find that elevated diastolic blood pressure is associated with these strains. Frequencies are available to subscribers.

Are Nanobacteria Making Us Ill?

Amit Asaravala  03.14.05 Wired 

Olavi Kajander didn't mean to discover the mysterious particles that have been called the most primitive organisms on Earth and that could be responsible for a series of painful and sometimes fatal illnesses.
He was simply trying to find out why certain cultures of mammalian cells in his lab would die no matter how carefully he prepared them.
So the Finnish biochemist and his colleagues slipped some of their old cultures under an electron microscope one day in 1988 and took a closer look. That's when they saw the particles. Like bacteria but an astonishing 100 times smaller, they seemed to be thriving inside the dying cells.
Believing them to be a possible new form of life, Kajander named the particles "nanobacteria," published a paper outlining his findings and spurred one of the biggest controversies in modern microbiology.
At the heart of the debate is the question of whether nanobacteria could actually be a new form of life. To this day, critics argue that a particle just 20 to 200 nanometers in diameter can't possibly harbor the components necessary to sustain life. The particles are also incredibly resistant to heat and other methods that would normally kill bacteria, which makes some scientists wonder if they might be an unusual form of crystal rather than organisms...

Work at Frequency Foundation has found nanobacteria directly associated with the following:

1. Elevated diastolic blood pressure.
2. Need for excessive sleep. A teenager needed 17 hours of sleep a day returned to normal within one day after applying nanobacteria frequencies.
3. Arthritis - nanobacteria is always associated with the aches and pains in joints, and probably with the deformation associated with neglecting this condition.
4. Artherosclerosis - always check the heart area with the MacArthur BioDisk
5. Immune dysfunction
6. Peanut and other allergies - a researcher in the U.K. had dark field blood microscopy that clearly showed nanobacteria in the blood. She had a life threatening peanut allergy. When the nanobacteria was removed the peanut allergy was almost completely eliminated. She needed no medication after eating peanuts. (Do not try this at home!)
7. Herxheimer effects from chelation therapy - chelation eliminates calcium from the system and releases nanobacteria. Frequencies should always be used in conjunction with chelation therapy.

New supplements for oral chelation using nanotechnology provide results equivalent to IV chelation. For example, with a blood pressure of 140/100 upon awakening, I used the infrared sauna and blood pressure went to 140/80. Then I took some Quicksilver Scientific Therasomal (EDTA with R-Lipoic Acid) and a Doctor's Best Red Yeast Rice for cholesterol and half an hour later my blood pressure was 120/80.

Then I tested with the MacArthur biodisk which checks for nanobacteria. I got a positive Aurameter reading by placing the biodisk next to my body in the abdominal area. This indicated the need to run nanobacteria frequencies which will always be needed when doing chelation.

07 February 2016

GcMAF and Nagalase 2.2

Always run Naglase frequencies for viruses and cancer. Physicians recommend 10,000 units of Vitamin D a day to promote effects of GcMAF.

Nagalase in Blood
Test for monitoring efficacy of therapy for cancer and certain viral infections

Nagalase in serum / plasma

The test measures the activity of an enzyme α-N-acetylgalactosaminidase (nagalase) in blood.
Nagalase is an extracellular matrix-degrading enzyme that is secreted by cancerous cells in the process of tumor invasion. It is also an intrinsic component of the envelope protein of various virions, such as HIV and the influenza virus. Thus, it is also secreted from virus-infected cells1,3,4.
Nagalase deglycosylates the vitamin D3-binding protein DBP (also known as Gc-protein). Gc-protein, which contains three sugars, is the precursor for the major macrophage-activating factor (MAF). By complete deglycosylation, Gc-protein can no longer be converted to MAF.
Normally, MAF is produced from the Gc-protein by sequential removal of the galactose and sialic acid without touching the remaining sugar N-acetylgalactosamine.
Macrophage activation for phagocytosis and antigen presentation is the first step in the immune development cascade. Lost precursor activity, therefore, leads to immune suppression.
Increased nagalase activity has been detected in the blood of patients with a wide variety of cancers like cancer of the prostate, breast, colon, lung, esophagus, stomach, liver, pancreas, kidney, bladder, testis, uterus, and ovary, mesothelioma, melanoma, fibrosarcoma, glioblastoma, neuroblastoma, and various leukemias1,3,4. For various types of tumors, various levels of nagalase activity were found7. It appears that the secretory capacity of individual tumor tissue varies among tumor types depending upon tumor size, staging, and the degree of malignancy or invasiveness7. Increased nagalase activity has not been detected in the blood of healthy individuals1.
Nagalase activity is directly proportional to viable tumor burden1,2. Studies correlating nagalase levels with tumor burden suggest that the measurement of this enzyme can diagnose the presence of cancerous lesions below levels detectable by other diagnostic means1. In research studies, nagalase activity decreased to near tumor-free control levels one day after surgical removal of primary tumors from cancer patients, suggesting that the half-life of nagalase is less than 24 hours1,6. The short half-life of nagalase is valuable for prognosis of the disease during various therapies1,5See HDRI ...

Here is a frequency set which could be the most useful set in your arsenal. Tim Smith, M.D. reports:

How GcMAF works: GcMAF is the protein that activates macrophages and jump-starts the entire immune response. To sabotage the immune system and put the macrophages to sleep, all cancers and viruses make Nagalese, the enzyme that blocks production of GcMAF. In the absence of GcMAF, cancers, HIV, and other viruses can grow unimpeded. Dr. Nobuto Yamamoto demonstrated that GcMAF administration bypasses the Nagalese blockage and re-activates the macrophages, which then proceed to kill the cancer cells and HIV viruses.

All substances can be disrupted by frequencies. We don't need GcMAF to bypass Nagalese. We can just eliminate the Nagalese. Running the program below yields a dramatic increase in immune response.

You will need to run the frequencies for several hours initially. Running them too much will start to make your energy low. The increase in immune function will cause your macrophages to attack cancer cells, viruses, and perhaps bifiolms and other organisms. The immune response may make you feel worse in the short term. Better Health Guy gives a good rundown on his experience with this.

Appropriate candidates for GcMAF treatment include:

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

Learn more: http://www.naturalnews.com/050972_GcMAF_cancer_cells_Bradstreet.html#ixzz3kMO73U00

Frequencies are available for subscribers.

31 January 2016

Zika Virus Version 1.0 - Six Strains

CDC photo of Zika virus

Several strains of the Zika virus have been in the Frequency Research Foundation database for years. However, a couple of new strains are virulent and can cause neurological symptoms and fatigue for an extended period of weeks or months until the virus is eradicated.

Frequencies sets for half a dozen strains have been sequenced for the Zika virus, including two of the new strains identified circulating in the United States. Subscribers will find them on the subscribers site.

Reuters - 25 Jan 2016

The virus was first found in a monkey in the Zika forest near Lake Victoria, Uganda, in 1947, and has historically occurred in parts of Africa, Southeast Asia and the Pacific Islands. But there is little scientific data on it and it is unclear why it might be causing microcephaly in Brazil. 

Laura Rodrigues of the London School of Hygiene and Tropical Medicine said it was possible the disease could be evolving. If the epidemic was still going on in August, when Brazil is due to host the Olympic Games in Rio de Janeiro, then pregnant women should either stay away or be obsessive about covering up against mosquito bites, she said. The WHO advised pregnant women planning to travel to areas where Zika is circulating to consult a healthcare provider before traveling and on return. 

The clinical symptoms of Zika are usually mild and often similar to dengue, a fever which is transmitted by the same Aedes aegypti mosquito, leading to fears that Zika will spread into all parts of the world where dengue is commonplace. More than one-third of the world’s population lives in areas at risk of dengue infection, in a band stretching through Africa, India, Southeast Asia and Latin America. 

Zika's rapid spread, to 21 countries and territories in the Americas since May 2015, is due to the prevalence of Aedes aegypti and a lack of immunity among the population, the WHO said in a statement.

Natural News:

"The Zika virus outbreak currently gripping the Americas could have been sparked by the release of genetically modified mosquitoes in 2012," reports The Mirror. "The insects were engineered by biotechnology experts to combat the spread of dengue fever and other diseases and released into the general population of Brazil in 2012... The Aedes aegypti mosquito sub-species that carries both the Zika virus and dengue was the type targeted with genetically modified mosquitoes."

But something went horribly wrong.

As pointed out in this fantastic article by AntiMedia.org, the genetic engineers running this massive open-air experiment with mosquitoes and humans failed to consider the impact of antibiotics in the environment caused by their heavy use in agricultural (animal feed) operations.

As AntiMedia reports:

Only the male modified Aedes mosquitoes are supposed to be released into the wild — as they will mate with their unaltered female counterparts. Once offspring are produced, the modified, scientific facet is supposed to ‘kick in’ and kill that larvae before it reaches breeding age — if tetracycline is not present during its development...

According to an unclassified document from the Trade and Agriculture Directorate Committee for Agriculture dated February 2015, Brazil is the third largest in “global antimicrobial consumption in food animal production” — meaning, Brazil is third in the world for its use of tetracycline in its food animals. As a study by the American Society of Agronomy, et. al., explained, “It is estimated that approximately 75% of antibiotics are not absorbed by animals and are excreted in waste.” One of the antibiotics (or antimicrobials) specifically named in that report for its environmental persistence is tetracycline.

The presence of antibiotics causes the mosquitoes that are supposed to die off to survive and reproduce. These same genetically engineered mosquitoes may then bite humans, injecting them with the Zika virus that's now causing horrific mutations in head and brain formation in children.

Learn more: http://www.naturalnews.com/052824_Zika_virus_genetically_engineered_mosquitoes_unintended_consequences.html#ixzz3yx5ltmjb

17 January 2016

Malaria Frequencies Version 6.0

In 2015 a lot of research time has been invested in studying malaria strains. It is quite easy to eliminate symptoms with frequencies. However, eradicating the disease long term requires a sophisticated approach. There are hundreds of strains of the malaria parasite and comprehensive frequency sets for each strain must be identified.

There are many people in the United States infected with malaria. Not only can you be exposed through travel - malaria strains have been circulating with the swine flu in recent years.

At the beginning of this year I went on a pilgrimage to India up the Ganges River on a river boat, stopping in many of the little villages along the way. My goal was to get to Bohdi Tree where the Buddha attained enlightenment. I was exposed to constant infection from many sources including mosquito bites with malaria strains. This gave me onsite experience in identifying new malaria strains, sequencing them, and running them on my portable F175 laboratory which I took with me on the river boat.

So over the last year:

1. Many new strains of the malaria parasite have been identified.
2. A template for all frequencies needed to eradicate a strain has been developed that has 61 frequencies for each strain of malaria!
3. Thousands of old frequencies from old strains have been updated to work more effectively.

Malaria Frequencies Version 6.0, available to subscribers on the subscribers site, is the most comprehensive and effective frequency set on the planet for dealing with malaria. Frequencies are regularly updated and improved on a weekly basis.

Malaria life cycle illustration.
National Institute of Allergy and Infectious Diseases

The malaria parasite is easily killed by electromagnetic frequencies and there are a number of small pilot projects using zappers in Africa. I've talked with some of the larger nonprofits about expanding these studies as I have seen 100% remission consistently with a few hours of application of exact frequencies. However, the response has been that if a non-profit research institute looked at anything other than conventional drugs they would get all their grants terminated.

It is important to keep up with the latest research on malaria as frequencies can also modify protein production. Virulent forms of this and other diseases (particular viral infections) can kill by evoking an overwhelming immune response. Thus frequencies must modulate immune response through reducing certain protein production as well as kill the pathogen.

Malaria has very distinctive symptoms which cycle in waves. See The Piano Tuner: A Novel. I read this book on an international flight when I was infected with malaria and had quite an experience.

17 November 2015

SV40 Version 2.0 Frequencies

Recent work on multiple cases of SV40 with related cancers led to significant updates to multiple strains of the virus using the latest frequency templates. Each virus strain has over two dozen frequencies which target the virus, all of the components of the machinery for the virus, the DNA of cells contaminated with the virus, and the energy system of the human body which is distorted by the virus. All frequencies are available to subscribers - see Paypal button at bottom right of page.

Bookchin, D. and J. Schumacher (2004). The Virus and the Vaccine: The True Story of a Cancer-Causing Monkey Virus, Contaminated Polio Vaccine, and the Millions of Americans Exposed. New York, St. Martin's Press.

Everyone infected with the SV40 virus should read this book and that includes at least 100 million Americans. The contamination of polio vaccine with the carcinogenic SV40 virus apparently continues even today in some cases. Information on the most carcinogenic of all viruses and its connection with polio vaccine has been systematically suppressed since the 1960's. Careers have been threatened, some destroyed, others altered dramatically. Funding for investigating what will come to be known as one of the greatest public health problems of the 20th century is still severely restricted.

The authors original article in the Atlantic Monthly (Feb 2000) has been expanded into a riveting book that reads like a novel. Extensively documented, it includes a complete bibliography of all research on SV40 and notes from interviews of every major player in this controversy who is still alive. The story would make a great episode for the X-Files and you might never look at the NIH in quite the same way again. The 2004 controversy over NIH officials acting as consultants for the drug companies is only the tip of the iceberg.

Char Boehme published a set of frequencies on the Rifers list (rifers@yahoogroups.com) developed from available DNA sequencing data. I have tested her frequencies against a known SV40 infection and they all test positive, demonstrating the value of DNA sequencing data and her technique. We both view this as a widespread public health problem generated by contaminated vaccines.

Parasites are often infected with SV40. When you kill them, they release more SV40. You may need to repeatedly clear your system of this virus after killing parasites. In addition, when killing cancer cells in SV40 induced tumors, the virus will be released and cause reinfection. Run SV40 frequencies after killing SV40 induced tumor cells. Finally, a magpulser will stimulate virus production in infected cells and this must be dealt with.

The SV40 virus appears to be unaffected by the homeopathic remedy Osscilicoccinum 200C. However, I recently achieved a positive effect with Dolisos Flu Solution (see http://www.dolisosamerica.com/).

On review of the medical literature, there are clearly multiple forms of SV40. One mutated form cannot replicate and there are others. See:

Simian virus 40 (SV40) DNA replication: SV40 large T antigen unwinds DNA containing the SV40 origin of replication. Dean FB, Bullock P, Murakami Y, Wobbe CR, Weissbach L, Hurwitz J. Proc Natl Acad Sci U S A. 1987 Jan;84(1):16-20.

Complete nucleotide sequence of SV40 DNA.
Fiers W, Contreras R, Haegemann G, Rogiers R, Van de Voorde A, Van Heuverswyn H, Van Herreweghe J, Volckaert G, Ysebaert M. Nature. 1978 May 11;273(5658):113-20.

The determination of the total 5,224 base-pair DNA sequence of the virus SV40 has enabled us to locate precisely the known genes on the genome. At least 15.2% of the genome is presumably not translated into polypeptides. Particular points of interest revealed by the complete sequence are the initiation of the early t and T antigens at the same position and the fact that the T antigen is coded by two non-contiguous regions of the genome; the T antigen mRNA is spliced in the coding region. In the late region the gene for the major protein VP1 overlaps those for proteins VP2 and VP3 over 122 nucleotides but is read in a different frame. The almost complete amino acid sequences of the two early proteins as well as those of the late proteins have been deduced from the nucleotide sequence. The mRNAs for the latter three proteins are presumably spliced out of a common primary RNA transcript. The use of degenerate codons is decidedly non-random, but is similar for the early and late regions. Codons of the type NUC, NCG and CGN are absent or very rare.

There is a new article out on the connection between cancer and the SV40 virus which is widely distributed in the human population because of polio vaccination contamination. NCI has followup studies on Army "volunteers" who were given contaminated polio vaccine in 1960-61.

Testing a volunteer (who was in the Army and given the vaccine in 1960) with a liver tumor and a history of melanoma and multiple basal cell carcinomas showed SV40 distributed throughout all organ systems. Plate zapping organ by organ was required to root it out.

I've noticed SV40 in several other cancer patients. Electronic medicine researchers should check each other for presence of this virus and eradicate it. SV40 causes cancer in lab animals, causes cells to become immortal in vitro, and is found in human tumors. It inactivates genes related to controlling cancerous growth. SV40 antibodies are present in 3-4% of the population. SV40 can start a tumor growing including cells that are not infected with HIV. The uninfected tumor cells have a selective growth advantage and replace infected cells, caused the SV40 virus to disappear. This stealth phenomena is one of the reasons it has been difficult to conclusively state that SV40 is causing cancer. However, for some tumors, the evidence is far stronger than smoking.

Simian virus 40 in human cancers
Regis A. Vilchez MD, Claudia A. Kozinetz PhD, MPH, Amy S. Arringtonc, Charles R. Madden PhD and Janet S. Butel PhD
The American Journal of Medicine Volume 114, Issue 8 , 1 June 2003, Pages 675-684


Many studies have reported the presence of simian virus 40 (SV40) deoxyribonucleic acid (DNA) or protein in human brain tumors and bone cancers, malignant mesothelioma, and non-Hodgkin's lymphoma. However, the small samples and lack of control groups in some reports have made it difficult to assess their reliability.

Studies were included in this analysis if they met the following criteria: original studies of patients with primary brain tumors and bone cancers, malignant mesothelioma, or non-Hodgkin's lymphoma; the investigation of SV40 was performed on primary cancer specimens; the analysis included a control group; and the same technique was used for cases and controls. Included reports were published from 1975 to 2002.

Thirteen studies fulfilled the criteria for the investigation of primary brain cancers (661 tumors and 482 control samples). Specimens from patients with brain tumors were almost four times more likely to have evidence of SV40 infection than were those from controls (odds ratio [OR] = 3.9; 95% confidence interval [CI]: 2.6 to 5.8). The association was even stronger for mesothelioma (OR = 17; 95% CI: 10 to 28; based on 15 studies with 528 mesothelioma samples and 468 control samples) and for bone cancer (OR = 25; 95% CI: 6.8 to 88; based on four studies with 303 cancers and 121 control samples). SV40 DNA was also more frequent in samples from patients with non-Hodgkin's lymphoma (OR = 5.4; 95% CI: 3.1 to 9.3; based on three studies with 301 cases and 578 control samples) than from controls.

These results establish that SV40 is associated significantly with brain tumors, bone cancers, malignant mesothelioma, and non-Hodgkin's lymphoma. Studies are needed to assess current prevalence of SV40 infections.


13 August 2015

PseudoScience: Is Evidenced Based Medicine Manipulated Evidence to Sell Bad Drugs?

Lies, Damned Lies, and Medical Science

Much of what medical researchers conclude in their studies is misleading, exaggerated, or flat-out wrong. So why are doctors—to a striking extent—still drawing upon misinformation in their everyday practice? Dr. John Ioannidis has spent his career challenging his peers by exposing their bad science.

Read all about it!

20 June 2015

Electronic Medicine Goes Mainstream

Stimulation of the nervous system could replace drugs for inflammatory and autoimmune conditions

Bryan Christie

In Brief

  • Exposure to heat, pressure, light or chemicals sets in motion a process to ensure that bodily organs do not overreact to these stresses.
  • Nerve signals that link the brain and the rest of the body inhibit the making of immune molecules that cause inflammation.
  • Electrical stimulation of neural pathways with an implanted medical device may assist the body in suppressing inflammation.
  • Bioelectronic medicine is the name of the new discipline that uses electrical stimulation to treat inflammation and other disorders.

More on this Topic

I am a brain surgeon who is fascinated by inflammation. Along with my laboratory colleagues, I examine molecules that cause inflammation so that we can discover methods for alleviating the pain, swelling and tissue damage that is a consequence of many diseases.
Some of this work has already benefited patients. In 1987 I published the results of an experiment that targeted an inflammatory molecule called tumor necrosis factor, or TNF, to rescue lab baboons from the consequences of lethal infection—a study that contributed to the discovery of a new class of drugs for inflammatory, autoimmune and other diseases that disrupt the normal functioning of the body's immunological defenses.
As a neurosurgeon, I am also intensely interested in the workings of the brain. A surprising discovery we made in the late 1990s, again involving TNF, merged insights from neuroscience and immunology. We inadvertently discovered that neurological reflexes—predictable responses to certain sensory stimuli—block the production of TNF. This insight culminated in an invention I devised to treat inflammation using small, electrical nerve stimulators implanted in patients.
The use of nerve-stimulating electronic devices to treat inflammation and reverse disability is laying the foundation for a new discipline called bioelectronic medicine. It is being tested in clinical studies of patients with rheumatoid arthritis and other diseases. It is based on a deceptively simple concept of harnessing the body's natural reflexes to develop an array of effective, safe and economical alternatives to many pills and injectable drugs. By precisely targeting the biological processes underlying disease, this nerve-stimulating technology should help avoid the troublesome side effects of many drugs.