16 May 2013

Heal Joints: Eliminate Arthritic Pain


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We're adding this all-natural product to our Longevity program. These are unretouched photos of the before and after effects. If you wish more information, please give Dale Fawcett a call at 360 598-6585 or email him at:  dale.fawcett@gmail.com.

20 April 2013

High School Student Wins Award and Publication for Showing Organic Food is Healthier


Figure 2. Daily egg-laying of flies exposed to organic diets.

Organically Grown Food Provides Health Benefits to Drosophila melanogaster

    Abstract

The “organic food” market is the fastest growing food sector, yet it is unclear whether organically raised food is nutritionally superior to conventionally grown food and whether consuming organic food bestows health benefits. In order to evaluate potential health benefits of organic foods, we used the well-characterized fruit fly Drosophila melanogaster as a model system. Fruit flies were raised on a diets consisting of extracts of either conventionally or organically raised produce (bananas, potatoes, raisins, soy beans). Flies were then subjected to a variety of tests designed to assess overall fly health. Flies raised on diets made from organically grown produce had greater fertility and longevity. On certain food sources, greater activity and greater stress resistance was additionally observed, suggesting that organic food bestows positive effects on fly health. Our data show that Drosophila can be used as a convenient model system to experimentally test potential health effects of dietary components. Using this system, we provide evidence that organically raised food may provide animals with tangible benefits to overall health.
Citation: Chhabra R, Kolli S, Bauer JH (2013) Organically Grown Food Provides Health Benefits to Drosophila melanogaster. PLoS ONE 8(1): e52988. doi:10.1371/journal.pone.0052988
Editor: Shree Ram Singh, National Cancer Institute, United States of America
Received: July 23, 2012; Accepted: November 27, 2012; Published: January 9, 2013

03 March 2013

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.

07 February 2013

EM Patent by Elizabeth Rauscher

United States Patent4,889,526
Rauscher ,   et al.December 26, 1989


Non-invasive method and apparatus for modulating brain signals through an external magnetic or electric field to reduce pain

Abstract
This invention incorporates the discovery of new principles which utilize magnetic and electric fields generated by time varying square wave currents of precise repetition, width, shape and magnitude to move through coils and cutaneously applied conductive electrodes in order to stimulate the nervous system and reduce pain in humans. Timer means, adjustment means, and means to deliver current to the coils and conductive electrodes are described, as well as a theoretical model of the process. The invention incorporates the concept of two cyclic expanding an collapsing magnetic fields which generate precise wave forms in conjunction with each other to create a beat frequency which in turn causes the ion flow in the nervous system of the human body to be efficiency moved along the nerve path where the locus of the pain exists to thereby reduce the pain. The wave forms are create either in one or more coils, one or more pairs of electrodes, or a combination of the two.

Inventors:Rauscher; Elizabeth A. (San Leandro, CA), Van Bise; William L. (San Leandro, CA)
Assignee:Magtech Laboratories, Inc. (Reno, NV) 
Appl. No.:07/120,914
Filed:November 13, 1987

Contact Dr. Donnie Rudd for a new low cost magnetic healing device based on this patent.

28 January 2013

Sodium Bicarbonate and Cancer


Bicarbonate Increases Tumor pH and Inhibits Spontaneous Metastases

  1. Robert J. Gillies3
  1. 1Arizona Cancer Center, University of Arizona, Tucson, Arizona; 2Department of Pharmacology, Wayne State University, Detroit, Michigan; and 3H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida
  1. Requests for reprints:
    Robert J. Gillies, H. Lee Moffitt Cancer Center, SRB-2, 12302 Magnolia Drive, Tampa, FL 33612. Phone: 813-725-8355; Fax: 813-979-7265; E-mail: Robert.Gillies@moffitt.org.

Abstract

The external pH of solid tumors is acidic as a consequence of increased metabolism of glucose and poor perfusion. Acid pH has been shown to stimulate tumor cell invasion and metastasis in vitro and in cells before tail vein injection in vivo. The present study investigates whether inhibition of this tumor acidity will reduce the incidence of in vivometastases. Here, we show that oral NaHCO3 selectively increased the pH of tumors and reduced the formation of spontaneous metastases in mouse models of metastatic breast cancer. This treatment regimen was shown to significantly increase the extracellular pH, but not the intracellular pH, of tumors by 31P magnetic resonance spectroscopy and the export of acid from growing tumors by fluorescence microscopy of tumors grown in window chambers. NaHCO3 therapy also reduced the rate of lymph node involvement, yet did not affect the levels of circulating tumor cells, suggesting that reduced organ metastases were not due to increased intravasation. In contrast, NaHCO3 therapy significantly reduced the formation of hepatic metastases following intrasplenic injection, suggesting that it did inhibit extravasation and colonization. In tail vein injections of alternative cancer models, bicarbonate had mixed results, inhibiting the formation of metastases from PC3M prostate cancer cells, but not those of B16 melanoma. Although the mechanism of this therapy is not known with certainty, low pH was shown to increase the release of active cathepsin B, an important matrix remodeling protease. [Cancer Res 2009;69(6):2260–8]

27 January 2013

Dana Ullman on Vaccines with References

Comments on the Vaccine Issue

--DANA ULLMAN, MPH
The scientist to win the 1st Nobel Prize in Medicine was Emil Adolph von Behring for his discovery of the diphtheria vaccine. He later acknowledged that he was inspired to do his research by homeopathy.  Although vaccinations and homeopathy are both based on the "principle of similars," these two treatments are also quite different.  Homeopathic medicines are used in much smaller and safer doses; they are usually prescribed with much greater individualization, and homeopathic medicines are used to both treat AND prevent disease, not just prevent disease.  

I am personally not "against" vaccines.  To be against vaccines is akin to be against surgery.  Both treatments have their place in health care, but each treatment is inappropriate for everyone, and numerous factors need to be considered before accepting them as a reasonable strategy.  First and foremost, living in a free society, I strongly believe that no drugs should be mandatory.  Second, vaccines are not always safe, and they can cause chronic ailments in rare situations (but such situations are more common than is commonly realized).  Third, some acute infections, such as chicken pox and measles, may actually be important for children to experience as a way to augment and strengthen their emerging immune and defense systems (did you know that children who get measles tend to have a significantly lower incidence of respiratory allergies).  Finally, the primary reason that homeopathy became popular in the 19th century in Europe and in the USA was the result of the impressive results that homeopaths experienced in treating the various infectious disease epidemics that raged during that era.  In other words, homeopathic medicines can be effective in treating many modern infectious diseases.

The following books will help you better understand the place for homeopathic medicines in the prevention and treatment of modern infectious diseases, and some of these books will also teach you how to treat some of the symptoms that vaccinations can cause.

The Vaccine Guide: Risks and Benefits for Children and Adults. Randall Neustaedter, OMD.  This book describes the risks of getting vaccinating for each of the common vaccines as well as the risks of not getting vaccinated.  This book has 40 pages (!) of references and is a practical guidebook to parents.  

Vaccine Free: Prevention and Treatment of Infectious Contagious Disease with Homeopathy (2nd edition), Kate Birch, RSHom, CCH, CMT.  This comprehensive book describes how to use homeopathic medicines to prevent diseases and which homeopathic medicines to use to treat them.  

The Solution: Homeoprophylaxis--The Vaccine Alternative. Kate Birch, RSHom, CCH, CMT, and Cilla Whatcott, HD, CCH.  This book is a shorter and well-illustrated book that will teach you how to use homeopathic medicines to prevent various ailments...and does so with clear and easy protocols.  It also lists the common homeopathic medicines to treat infectious diseases, but it doesn't provide detailed information about each remedy in such treatment.

Vaccine Damaged Children: Treatment, Prevention, Reasons.  Isaac Golden, PhD. No single book can be a guide to the treatment of children who experience side effects from vaccines, but this book is a good first place to start.  Generally, one must go to a professional homeopath for individualized care, but this book will teach you why homeopathy should be considered in such instances.

The Complete Practitioner's Manual of Homoeoprophylaxis.  Isaac Golden, PhD.  This book provides detailed information on how to use homeopathic medicines to help prevent ailments. This book also reviews recent research, including a large study in Cuba, that shows significant reduction with the proper use of homeopathic medicines.

02 January 2013

Pulsed Electric Fields Kill Melanoma



The publisher's final edited version of this article is available at Biochem Biophys Res Commun
See other articles in PMC that cite the published article.

Abstract
We have discovered a new, drug-free therapy for treating solid skin tumors. Pulsed electric fields greater than 20 kV/cm with rise times of 30 ns and durations of 300 ns penetrate into the interior of tumor cells and cause tumor cell nuclei to rapidly shrink and tumor blood flow to stop. Melanomas shrink by 90% within two weeks following a cumulative field exposure time of 120 μs. A second treatment at this time can result in complete remission. This new technique provides a highly localized targeting of tumor cells with only minor effects on overlying skin. Each pulse deposits 0.2 J and 100 pulses increase the temperature of the treated region by only 3 °C, ten degrees lower than the minimum temperature for hyperthermia effects.

29 December 2012

Dr. Sircus.com on Pulsed Electromagnetic Field Therapy


Pulsed Electromagnetic Field Therapy for Cancer and Pain

An FDA-Approved Cancer Treatment

Description: http://www.chronicpainreliefnow.com/images/microcurrent-met.jpg
Novocure™ has a new FDA-approved weapon (NovoTTF-100A System™) for patients and physicians in the battle against cancer (specifically for treating recurrent brain tumors). Microcurrent therapy is a novel anti-mitotic treatment that has been shown to slow or reverse tumor progression by inducing cell death in certain solid tumors. Their microcurrent device will be available for prescription use in the U.S. initially through several noted brain cancer research centers.
Pulsed electromagnetic field (PEMF) therapy has been used to treat almost every conceivable human illness or malady, including many inflammatory diseases such as arthritis or psoriasis and you don’t have to wait for the FDA to approve this treatment for your kind of cancer. All you have to do is choose among the many options in terms of equipment.
Pulsed electromagnetic field therapy (PEMFT), also called pulsed magnetic therapy, pulse magnetotherapy, or PEMF, is a reparative technique most commonly used in the field of orthopedics for the treatment of non-union fractures, failed fusions, congenital pseudarthrosis and depression. In the case of bone healing, PEMF uses electrical energy to direct a series of magnetic pulses through injured tissue whereby each magnetic pulse induces a tiny electrical signal that stimulates cellular repair.
Many studies have also demonstrated the effectiveness of PEMF in healing soft-tissue wounds, suppressing inflammatory responses at the cell membrane level to alleviate pain and increase range of motion. The value of pulsed electromagnetic field therapy has been shown to cover a wide range of conditions, with well-documented trials carried out by hospitals, rheumatologists, physiotherapists and neurologists. In years past this has been a very expensive form of therapy using sophisticated equipment, but that has all changed.


For more, see:
http://drsircus.com/medicine/cancer/pulsed-electromagnetic-field-therapy-cancer-pain

02 December 2012

Biofioms: Only Frequencies Can Eliminate Them

Bacterial communities just like these thrive on your gums and teeth (and everyone else’s too).
By Ronald Ordinola Zapata (Own work) [CC-BY-SA-3.0 (http://creativecommons.org/licenses/by-sa/3.0)], via Wikimedia Commons


Engineering Biofilms - ResearchPennState
Understanding how bacteria function in communities could lead to a host of new applications.
“Anywhere there’s a surface and water in the liquid state,” Tom Wood confirms, “you’re going to have biofilms.”

In riverbeds and showerheads. On the hulls of ships and inside pipelines. On contact lenses and joint prostheses and the gleaming white surfaces of your teeth. Biofilms, says Wood, professor of chemical engineering and biochemistry at Penn State, “are communities of bacteria that have the ability to cement themselves to a solid surface, and then—if you picture them in a river, say—rather than going with the flow they anchor down to a rock, and as the river goes by they get the nutrients they need and they’re able to thrive.”

“Communities” is the operative word. The biofilm that coats your teeth harbors more than 300 species of bacteria, working in concert. Most of these microbes either do no harm or are actually beneficial, but the few bad actors can saddle you with tooth decay and gum disease.

Biofilms cause corrosion, a huge economic drain on industry and infrastructure, and are also increasingly recognized as a leading culprit in chronic disease, from childhood middle-ear infections to cystic fibrosis. Hospital infections are largely due to their ubiquitous presence.

“In joint replacement surgery,” Wood says, “if an infection takes hold, there’s no drug they can add to get rid of it. They have to go back in, take out the original prosthesis, and put another one in—and hope the same thing doesn’t happen all over again.” Over 65 percent of all microbial infections are attributable to biofilms, according to the National Institutes of Health.

These complex microbial communities, in short, cause a variety of problems, both inside the human body and out. But they also have the potential to do great good, from wastewater treatment to oil-spill clean-up to producing alternative fuels—if their biochemistry can be controlled. Wood believes that it can.

“The whole idea of my lab,” he says, “is that if we can understand the genetic basis of biofilm formation, then we can either get rid of a biofilm, or promote it to do whatever we want.”

Sleeper Cells
The Dutch scientist Anton van Leeuwenhoek first noticed biofilms back in 1683. When placing a scraping of plaque from his own teeth under one of his first-generation microscopes, he spotted a host of “very little living animalcules, very prettily a-moving.” For most of the next 300 years, however, biofilms were largely ignored, as microbiology focused on individual organisms in their free-floating, or planktonic, state.

“But bacteria do have this desire to hunker down and form an attachment to a solid surface,” Wood says. “That’s the way they are in nature, primarily—living in communities. Over the last couple of decades, scientists have started to look at that state, and there’s been an exponential increase in biofilm literature and studies. There’s now even a mouthwash that talks about including anti-biofilm compounds—so the public’s waking up to it, too.”

Living in communities, bacteria are much hardier than when floating around free. They’re far more resistant to antibiotics—up to a thousand times more resistant, according to common estimates. “They’re much harder to kill,” Wood acknowledges, “but they’re even trickier than that.” Standard antibiotic treatments, he notes, target bacteria that are growing, dividing, evolving. “But in a biofilm, up to 10 percent of the population is not actively metabolizing.”

Under antibiotic attack, Wood explains, these bacteria in effect “put themselves to sleep” to avoid destruction. “If a cell is asleep, not dividing, the antibiotic has no effect,” he says. Then, when the coast is clear and the drug has run its course, these sleeper cells have the ability to wake themselves up and kick off a whole new infection.

Appropriately, they’re called persisters. Their discovery is fairly recent, and when and how they work are hot topics among researchers of infectious disease. “What’s really fascinating to me,” Wood says, “is that they don’t undergo genetic change at all. There’s no mutations, no change in the DNA. It’s the opposite of building up genetic resistance.”

For the full article click here ...

Periodontal Biofilm Frequencies
Frequency Foundation subscribers have access to an extensive set of biofilm frequencies directed at gum disease. The organisms can travel throughout the body and cause heart disease, joint problems, digestive issues, and many other problems.

27 November 2012

Shingles Frequencies Version 2.0: You Will Need Them As You Age!


      from Wikipedia
Herpes zoster (or simply zoster), commonly known as shingles and also known as zona, is a viral disease characterized by a painful skin rash with blisters in a limited area on one side of the body, often in a stripe. The initial infection withvaricella zoster virus (VZV) causes the acute (short-lived) illness chickenpox which generally occurs in children and young people. Once an episode of chickenpox has resolved, the virus is not eliminated from the body but can go on to cause shingles—an illness with very different symptoms—often many years after the initial infection. Herpes zoster is not the same disease as herpes simplex despite the name similarity (both the varicella zoster virus and herpes simplex virus belong to the same viral subfamily Alphaherpesvirinae).
Varicella zoster virus can become latent in the nerve cell bodies and less frequently in non neuronal satellite cells of dorsal rootcranial nerve or autonomic ganglion,[1] without causing any symptoms.[2] Years or decades after a chickenpox infection, the virus may break out of nerve cell bodies and travel down nerve axons to cause viral infection of the skin in the region of the nerve. The virus may spread from one or more ganglia along nerves of an affected segment and infect the corresponding dermatome (an area of skin supplied by one spinal nerve) causing a painful rash.[3][4] Although the rash usually heals within two to four weeks, some sufferers experience residual nerve pain for months or years, a condition called postherpetic neuralgia. Exactly how the virus remains latent in the body, and subsequently re-activates is not understood.[1]
Throughout the world the incidence rate of herpes zoster every year ranges from 1.2 to 3.4 cases per 1,000 healthy individuals, increasing to 3.9–11.8 per year per 1,000 individuals among those older than 65 years.[5][6][7] Over a lifetime, a large fraction of people develop herpes zoster, though usually only once – in a 1960s US study, 50% of individuals living to age 85 had at least one attack, while 1% had at least two attacks.[8] Antiviral drug treatment can reduce the severity and duration of herpes zoster if a seven-to-ten day course of these drugs is started within 72 hours of the appearance of the characteristic rash.[5][9]

A recent full blown case of shingles (hospital diagnosed) in a client allowed identification of many strains of the shingles virus. The rash was stopped from spreading immediately with frequencies and the client was puzzled as to why she had such a mild cash of shingles after going to the hospital emergency room prior to frequency application.

Upon further investigation, the client slept in a houseboat in Amsterdam that had mosquitos infected with the shingles virus. A mosquito bite on the leg started the shingles rash. Because she had latent shingles virus from smallpox in childhood, she developed a full blown infection. The houseboat was cleared of mosquitos using the Frequency Foundation Mosquito Service and cleared of the shingles virus with the shingles frequencies. It turns out that there are many strains of the shingles virus that must be eliminated!

The Life Extension Foundation reported the following in December 2012:

Following a chicken pox infection, the virus (called varicella-zoster, or VZV) takes refuge in nerve cells. With the onset of immunosenescence, it's only a matter of time until the virus can reemerge to trigger an attack of shingles. Here are some surprising fiures about this classic illustration of immunosenescence at work.
  • More than 90% of adults harbor the VZ virus, and there is no means of predicting when or in whom a shingles outbreak will occur.
  • It's estimated that 1 million new cases of shingles occur in the US each year, resulting in up to 60,000 hospitalizations.
  • Your risk of developing shingles is about 1 in 3.
  • With advancing age, your risk of developing shingles goes up dramatically: by age 85, 50% of people have had at least one outbreak.
  • The severity of a shingles outbreak increases with age.
As a result over 90% of adults will benefit from running shingles frequencies to clear the virus from their body. Additional strategies for reversing immunosenescence are also recommended.

Frequencies are available with a subscription to the Frequency Foundation.

19 November 2012

Frequency Subscription and Photoanalysis

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Photo Analysis and Frequency Transmission

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11 November 2012

Tuberculosis Frequencies Version 3.0


An Armenian doctor showing chest x-rays used to track a patient's tuberculosis that has been resistant to drug therapy.
By NICHOLAS D. KRISTOF
Published: New York Times, December 6, 2008

Update 11 Nov 2012: Tuberculosis frequencies have been repeatedly updated since 2008 and Version 3.0 is available. Certain strains of the swine flu included tuberculosis. In the opinion of this researcher, most deaths due to swine flu were caused by the swine flu viruses, bacteria, and parasites combined with tuberculosis. In addition, more virulent strains of tuberculosis have appeared, even more resistent to antibiotics than XDR tuberculosis.

This means that those interested in the latest tuberculosis frequencies should subscribe to the Frequency Foundation list where all updates are posted. See this link ...

Original Research on XDR-Tuberculosis
Version 2.2 – 20 December 2008
©Frequency Research Foundation 2005-2008
Creative Commons License
XDR-TB: Tuberculosis Frequencies Version 2.0 by Jeff Sutherland is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 3.0 United States License. Based on a work at frequencyfoundation.com.

All frequencies are based on original research on thousands of people, animals, microscopic slides, and high-resolution digital photos and microscopic images of the actual organisms. The Frequency Foundation database contains many gigabytes of original raw frequency data from a decade of research and these data are researched and refined to continually update frequency sets. For questions, errors, or omissions contact: info@frequencyfoundation.com. Frequencies are for research purposes only and may be helpful, harmful, or ineffective depending on how they are used. These programs may generate negative side effects in the form of Herxheimer reactions or other phenomenon and are only to be used by other researchers for experimentation at their own risk.

Upgrade to Version 2.2

Ongoing research added another strain of XDB-TB and parasites associated with this organism.

Upgrade to Version 2.0

The New York Times recently provided new photos on a case of drug resistant tuberculosis that are useful for enhancing the tuberculosis frequency set. Many cases have been examined by the Frequency Foundation through electronic media and all cases have the same virus associated with the tuberculosis organism. This virus has been added to the frequency set. It appears that a number of persistent bacteria harbor a virus that helps protect them by reducing immune function and, in this case, reducing respiratory function. Fortunately, it is remarkably easy to eliminate this complex of organisms with frequencies.
From the point of view of frequency research, XDR-TB, MDR-TB, and TB are very different organisms. Each is included in the attached frequency set. There may be additional strains and there may be other helper viruses. That is a topic for future research when modifications are needed to eliminate new strains of the organisms.
In the 1980’s, after spending many years as a professor at the University of Colorado School of Medicine, it was clear that drug technology is a 1940’s technology that will not take us into the future. Suppression of innovation in medicine by business interests has assured that we will not have the technology of the future until enough people die unnecessarily that people start demanding something different. For example, I recently suggested to a physician at one of the world's largest non-profit organizations trying to eradicate tuberculosis and malaria that they try some frequency work. I was told if they experimented with frequency devices they would lose all their grants. Innovation is being systematically suppressed by your government and your physicians are living in fear of losing their livelihoods.
Imagine if IBM has been able to suppress chip innovation. We would have to build a laptop with vacuum tubes and use a truck to haul it around. This is the situation we are in with drugs. Innovation in electronics can completely replace drugs. The healing tool of the future will be our laptop or smartphone. It will have a database for frequency transmission that can emulate any drug. Frequency Foundation is already using technologies that detect and prevent disease before you even know you have it.
It would be an excellent idea to experiment with and gain an understanding of how to use the tuberculosis frequencies with the many Rife technologies widely available on the market. Because about 1/3 of the population has latent infections with tuberculosis organisms, you may need to eliminate a ticking time bomb that can erupt when your immune system is suppressed for any reason.
It will take a worldwide grass roots movement to eliminate XDR:TB so I am releasing the frequencies under a Creative Commons License that allows anyone to use them for non-commercial purposes with attribution.
#XDR-TB
#repeat will vary with organism and technologies
repeat 10
program c
vbackfreq a 0.002478752 0 66.6
vbackfreq b 0.049787068 0 66.6
#parasite associated with XDR-TB 20081212
fuzz .034% 1
685677 #444544 424467 344444 244666 144644 74466 44454 26666
#268666 12666 #XDR-TB strain 1
#286566 12666 #XDR-TB strain 2
#use sweep to clear drug resistant strains
dwell 10
sweep 12346 12944 1
sweep 268166 269054 1 #268666 12666 #XDR-TB strain 1
sweep 286054 287000 1 #286566 12666 #XDR-TB strain 2
dwell 360
fuzz .044% 1
434324 414422 364443 243333 143332 77565 44443 24343
dwell 90
#XDR-TB virus 20081212
fuzz .0013% 1
19623443 18444444 17443344 16453343 15444433 14433344 13334443 12344444 11434334 10433334
9444343 8444333 7443333 6343443 5434334 4433443 3433423 2444355 1576567
fuzz .044% 1
944446 844554 743443 666665 544545 433676 334466 243665 165765 95534 84544 74657 64446
fuzz .044% .1
56654 45345 24455 14344 6446 3345 2443 1444 766 444
dwell 360
fuzz .034% 1
234344 #MDR-TB
244344 #Mycobacterium tuberculosis
converge .024% 1
288666 #Tuberculosis miasm strain
converge 0.016% .1
12567.6 # protein
1662 2774
11777
end repeat
The frequencies are in F100 programming language format. This is thoroughly documented at atelierrobin.net.
Ongoing research will update these frequencies. For documentation of these frequencies and to obtain updates to these and many other frequency sets you can subscribe to the Frequency Foundation by clicking on the button below. Be advised that these frequencies will be upgraded as organisms mutate based on ongoing research and only subscribers will receive updates.