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Jeff Sutherland

Twice the Energy with Half the Stress

Uncovering the Role of Rife Organisms in Cancer Development

The original Rife organism, which appears to be a necessary condition for cancer cells to survive, has many strains and is highly persistent. The so-called Rife BX/BY “virus” is now believed to not be a virus, but rather a filterable, polymorphic, cell-wall deficient bacteria similar to Bacillus licheniformus. This is comparable to the Gregory cancer “virus,” which also replicates through cell replication – a characteristic that disqualifies it from being a virus. Both organisms are present in every cancer patient.

Almost all individuals with cancer are infected with Bacillus lichenformis. In order to effectively address cancer using electronic means, it is crucial to first eliminate all Bacillus lichenformis from the body, as it functions as both a tumor promoter and a mutagen. Tumors are more likely to grow or recur when this organism is present.

Many researchers may be unaware of a note in The Lancet, a leading medical journal, in which scientists reported having DNA sequenced the “cancer germ.” British researchers isolated and DNA sequenced what appears to be the Rife “filterable bacteria.” Bacillus licheniformis is a pleomorphic organism that can take the form of rods, cocci, and fungus-like structures. Rife faced significant challenges in culturing this organism in the 1920s, and researchers have had limited success since then. Thus, demonstrating non-contaminated multiple forms of the same organism with identical DNA sequences is a significant accomplishment that could resolve decades of controversy.

Reference: Sansom, Clare. “Cancer Germ” Bacteria Isolated. THE LANCET Oncology, Vol 4 February 2003, p. 63. (A free Lancet account is required to view this document.)

An article titled “Cancer Germ” Bacteria Isolated, published in The Lancet Oncology on February 1, 2003, and written by Clare Sansom, reports on a study by researchers at the University of Nottingham in the UK. This study discovered that Bacillus licheniformis was present in the tumors of breast cancer patients, suggesting that the bacterium may play a role in cancer development.

Summary of the study:

  • Researchers collected tumor samples from 20 breast cancer patients.
  • Bacillus licheniformis was found in the tumors of 18 patients.
  • The bacterium was absent in control samples taken from healthy tissue.
  • Researchers propose that the bacterium may contribute to cancer development by promoting inflammation and cell proliferation.

This study is the first to identify a bacterium potentially involved in breast cancer development. The findings could pave the way for new preventative measures and treatments for the disease.

Milton Wainwright previously published data indicating that bacteria can pass through very small holes (as noted by Rife) and that this has significant implications for their role as pathogens. See: Med Hypotheses 2002 Jun;58(6):558-60.

Energy Balancing by Numbers

Healing occurs when there is a shift between the harmonious and disharmonious energies in the body. To make that shift, you need a way to dialogue with your energetic field.

All organisms, including you, communicate by vibrational energy.  Your cells will use this vibrational energy first before using the chemical communication system of your body.

Manipulating this vibrational energy is much more efficient than giving chemicals to the body.

In Energy Balancing by Numbers, Lloyd Mear provides the source codes for this vibrational energy in the form of numerical sequences. These numerical sequences hold a charge, an intention, and they activate specific frequencies that should be present in a healthy body. They bring the body back online.


A colleague looking for a simple way to use frequencies recently asked me if Lloyd Mear’s frequencies worked. I tested them out and sure enough, they work simply by speaking the numbers. So anyone can do this using their own body as the frequency transmitter.

Even more interesting, as I started to us frequency hardware to transmit the frequencies, the colleague pointed out that the spoken energy numbers are not the same as Rife frequencies. To get the equivalent Rife frequency, you need to raise the spoken frequency to the power of 1/PHI. PHI is the golden mean = 1.618033 and the power of PHI is an interesting study in and of itself.

So let’s take an example. This morning I got up and took out the three page check list that comes with Lloyd’s book. Using muscle testing or my Cameron Aurameter, I found the second page of the checklist was where to look. Scanning page two, the item “Lungs – Strong L R” stood out. Specifically, my left lung was not as energized as it could be. The check list pointed to page 54 in Energy Balancing by NumbersThe first number on page 54 “Lungs 48683857365” tested positive. I then tested the application of the number by the spoken word and found it needed to be tuned up (common when working with frequencies) and the best number is 48683868365. Most of Lloyd’s frequencies work straight out of the book without tuning. I had to speak this number 10-15 times to get the desired effect which was a noticeable change in lung function and significant change in energy of the left lung.

This number can be turned into a frequency that I can transmit using an F165/Harmony Chip/DMI/SG1 combination by raising it to the power of 1/PHI.

48683868365 ^ (1/1.618033) = 4028758.792

This allows you to create frequency sets for remote balancing or imprinting on water. Even more amazing, you can take any Rife frequency and turn it into an effective spoken number by raising it to the awesome power of PHI. Let’s say you had an original Rife frequency of 12832676.

12832676 ^ 1.618033 = 317315912654.52 is the power of the spoken word.

One of my business partners (may he rest in peace) always said the ultimate frequency transmitter is the human body. Here you have it in a way anyone can use it!

Carcinogenesis: Preventing it with electronic medicine

Update: This original Rife organism appears to be a necessary condition for cancer cells to survive. Eliminating this organism causes cancer cell death. There are many strains of this organism and it is very persistent.
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As medical research advances, the strategy of systematically eliminating cancer cells with electromagnetic frequencies is entering the mainstream. A recent clinical trial showed clearly that low voltage application of frequencies destroys cancer cells, although their approach would need significant modification to be fully effective. Clinical trials have begun and electromagnetic frequencies have been approved by the FDA to treat certain tumor types. A remarkable video by Bill Doyle shows frequencies disrupting growth of cancer cells.

There are several steps to  dealing with cancer cells:
1. Nutritional and lifestyle factors described elsewhere are critical
2. Eliminate the Rife BX BY complex
3. Eliminate the Gregory cancer virus
4. Eliminate parasites that promote tumor growth
5. Disrupt glucose metabolism of cancer cells
6. Eliminate viruses that cause malignant cells
7. Target specific malignant cells for elimination

——
There is abundant epidemiological data from all over the world on cancer incidence for a wide variety of tumors in animal and human populations. My thesis advisor was Editor of the Journal of the National Cancer Institute in the late 1970s and early 1980s. He gave me a stack of over 300 papers from the medical journals with carcinogenesis dose reponse curves for many different species. All the curves looked different. He told me to explain why they were all different and he would give me a Ph.D. I then spent about 8 years doing supercomputer mathematical analysis of data on various types of cancer. The final data set I focused in on for publication was data from the Third National Cancer Survey which had complete coverage from many states in the U.S. and was the best available data at the time. My thesis advisor had led the survey and I had complete access to all data at the National Cancer Institute. The core model we developed is now the generally accepted model for carcinogensis. It was initially validated for colon cancer. See:
Sutherland, JV and Bailar, JC. The multihit model of carcinogenesis: etiologic implications for colon cancer. J Chronic Dis. 1984;37(6):465-80.

For most human cancers, the data clearly shows a four hit process. This can be visualized most clearly in skin tumors. An abnormal cell appears and begins dividing and creates a small patch on the skin. Within this lesion, a cell mutates, and you have a small patch growing within a patch. This happens a third time, then a fourth time. On the fourth genetic change, the cell breaks through the mechanisms that control proliferation and is malignant. It grows uncontrollably in a fifth phase, with the right promoting environment available, and can get into the bloodstream and migrate to other parts of the body causing metastases.

I have repeatedly seen the frequencies 2008 and 2127 appear in myself and others after eating certain food. I have been able to confirm that this has happened in most people who have eaten a specific meal. This is the BX and BY “virus” form of Rife’s organism. Today, this is not believed to be a virus and some think it is a mycoplasma. Recent DNA sequencing of organisms found in cancer cells showed them to be a fungus.

These organisms are clearly not a typical virus. They immediately go systemic throughout the entire body. And it originally took days of repeated treatment for long periods with the FSCAN and/or EM6+ to clear the body of them. With newer technologies they can be eliminate a lot faster.

However, more and more evidence is appearing that shows cancer cell frequencies are specific frequencies in a virus sequence. It appears that a virus disrupting the cellular machinery is one of the critical steps (but not the only step) that produces a tumor. Therefore, eliminating the relevant viruses is critical to prevent ongoing appearance of pre-malignant or malignant cells.

I have repeatedly seen non-malignant skin tumors grow quickly and in one case apparently become malignant in the presence of BX and BY. In the presence of this organism it is common to have tumors erupt in less than a day. This helps to explain an interesting aspect of my previous research in carcinogenesis. In some tumors, prostate for example, the data show that the first malignant cell appears 35 years before clinical diagnosis on the average. In a fast growing tumor like lung cancer, the first malignant cell appears about a year before clinical diagnosis. However, it is very common to see people go downhill extremely quickly after initial diagnosis. While some of this is undoubtedly due to the shock of the diagnosis and resultant depression of the immune system, it is aggrevated by the BX and BY virus. Much of conventional cancer treatment does not eliminate the virus and may even promote its growth.

So the BX and BY organisms are strong promoters of at least stage 3 (premalignant) and stage 4 (malignant) tumors and may even promote earlier stages. As indicated in the paper by Owens DM, Wei S, Smart RC. A multihit, multistage model of chemical carcinogenesis. Carcinogenesis, Vol. 20, No. 9, 1837-1844, September 1999, promotion of early phases of tumor initiation increases the cellular population at risk of mutating into a subsequent phase. This process happens so fast in the presence of BX and BY that I believe the Rife organisms are both promoters and mutagens.

The first approach to stopping proliferation of tumors must be to eradicate the BX and BY virus. Parasites also release substances that promote tumor growth so they must be eliminated as well. However, they are not as dangerous as BX and BY. I believe if everyone was monitored for BX and BY and the infection was eliminated immediately, we could significantly cut cancer incidence in the U.S., probably by more than 50%.

The fact that this information has been available for almost 100 years now shows how closed mindedness and suppression of innovation has compromised American medicine. This phenomenon has largely been driven by business interests, initially by a director of the AMA who was ultimately convicted of fraud and conspiracy for suppressing cancer therapies, and in more recent years by the pharmaceutical industry.

The tumors I have worked with (lung, cervix, skin, colon) have all had the presence of BX and BY which can be eliminated straight away. It is important to realize when targeting the BX and BY organisms with an electronic device that when you kill one strain, another strain proliferates and the frequency changes. These organisms have very stable frequencies around 2008 and 2127, however, and I have seen them deviate only by 3HZ at the most. It is important to eliminate all of them and you must have the exact frequency to 1HZ and this frequency may vary between 2003-2010 and 2125-2130. In recent years, the frequency set for BX BY has expanded to hundreds of frequencies.

Eliminating the BX and BY organism does not stop cells which have already reached stage 4 and are malignant. In fact, all malignant tumors will not show BX and BY present. They can continue to proliferate and metastasize without BX and BY. The best way to eliminate the malignant cells is to stop the ATP metabolism in these cells while leaving normal cells unaffected. This will prevent mitosis and the cancer cells will die a normal death without proliferating. This appears to be possible with frequencies in the 11,700,000 range. These frequencies also seem to stop mitosis of stage 3 cells as well. The data in the Gorgun paper shows how this is possible.

Gorgun SS. Studies on the Interaction Between Electromagnetic
Fields and Living Matter Neoplastic Cellular Culture. Frontier Perspectives 7:2:44-59, Fall 1998.

Stopping cellular mitosis requires the exact frequency. I have seen frequencies in the range 11,600,000 – 11,900,000HZ affect tumors. Different tumors of the same type (or perhaps cells in different stages) will have slightly different frequencies. Metastatic tumors will have different frequencies. They must all be eliminated systematically, one by one.

I believe that Rife was able to affect a “cure” in almost every case because his device running at 11,700,000 had enough variability and harmonics to stop mitosis in all relevant cells, even though their frequencies may have been slightly different. The curse of modern technology is that it is so precise, most people are unable to reproduce Rife’s work.

Richard Loyd had a machine some years ago that could treat directly at 11,700,000HZ. Most of us are not so lucky. I have found some success, however, in using the FSCAN to treat all the octaves of the exact frequencies in the FSCAN range from 10-3,000,000HZ. More recent FSCAN devices work in the 11-12MHZ range. Current frequency sets provided to Frequency Foundation subscribers go well over 30MHZ to target viral patterns in the bodies energy field. It will be difficult but not impossible, in my view, to stop all cellular mitosis using a Rife device that can only treat at less than 10,000HZ.

These comments represent a working hypothesis that has been successful in many cases and not as successful in rapidly growing tumors. It needs further research and new data may alter the working hypothesis. I present it so that others can take a look and see if they can produce the same results consistently.

More on Rife BX/BY Virus and Bacillus Licheniformis

Date: Sun, 24 Oct 2004 01:01:13 -0400
From: “CB”
Subject: thoughts on Bacillus licheniformis

Hello rifers,

There has significant discussion in the past year about an organism called Bacillus licheniformis and its probable connection to cancer, and possibly to Rife’s BX virus. In particular there has been a reference to an article which appeared in the journal Lancet. Discussion on these lists contained implications that the researcher reviewed in this article may have identified the BX viral organism. The article is available for free reading at http://oncology.thelancet.com/journal/vol4/iss2/full/lonc.4.2.newsdesk.24220.1, (required free registration with Lancet is available on the same page).

This subject just came up again on another list. Here is a copy of what I posted, with a few additional comments.

A check of the Lancet article referred to above shows it does not make any mention whatsoever of Rife, and the word “virus” never appears. The writer of this article reviews the work of a researcher that worked with the pleomorphic transformation of Helicobacter pylori to Bacillus licheniformis. Indeed a very interesting piece of work. He also sent samples of 16S ribosomal RNA in for sequencing, which revealed a connection to B licheniformis. However, viruses never contain any ribosomal RNA. The genome size of B. licheniformis is way beyond the range of any known viruses, and is much more in common with bacterial genome sizes.

Ribosomal RNA is necessary for cells and bacteria to make their proteins. But viruses also need to produce their proteins, and will hijack the ribosomal RNA machinery present in the cell that they are parasitizing, so to speak. Certain viruses will also enter bacterial pathogens and use the machinery. The particular cells or bacteria that viruses choose to enter, depend on whether an appropriate receptor is available for the virus to latch onto (along with other associated conditions).

It seems unrealistic to call B. licheniformis a virus. Conversely, one might then want to argue that Rife’s BX could be a bacteria. However, Rife gave very specific measurements for the organism he called BX, and it is totally in line with dimensions of viruses. This is not to deny the pleomorphic possibilities of his “BX”; indeed pleomorphic events have been amply demonstrated and reported over the past century in numerous organisms, and Rife achieved that as well with the BX. But to call a bacteria a virus (or vice-versa), only confuses the issue and actually serves to cloud the phenomenon of pleomorphism.

I am convinced nonetheless that the frequencies Jeff Sutherland posted specifically for the B. licheniformis (2655 and 21554) can be valid and effective. Jeff does very high-quality work. And that he is correct in reminding folks any approaches to cancer need to be broad-based. B. licheniformis and the BX viral form may both be present in many cancer situations, and / or co-participants in a line of pleomorphic events.

One of the John Marsh CDs available from Jeff Garff (#8) has Rife speaking very clearly and in some detail about his culture work with the BX, and the materials he used to get the various pleomorphic forms. Interestingly, Rife also states that he was able to isolate the BX from some “pyloric stomach cancers”. So here we may have an entire set of clues that at least for stomach cancers, there may be H. pylori, B. licheniformis, and BX virus involved as bacterial, fungal, and viral forms.

Best wishes,
Char

More Questions on the Rife “cancer virus”

I continue to get email questioning the frequencies posted for the Rife pleomorphic organism that is almost always associated with malignancies. Why are there numbers greater than 10000? Why don’t 2007 and 2128 posted on web site work? Why are there so many frequencies? Are these frequencies in megahertz. And so forth …

The “Rife” numbers posted on web sites are actually numbers created by Crane, an associate of Rife. For some reason he divided Rife’s numbers by 10. For an equally strange reason, they work, but only for certain forms and certain strains of the Rife pleomorphic organism, now thought to be Bacillus licheniformis. From what I know, Rife never used numbers below 10000 in his own work.

The Crane numbers 2007 and 2127 are useful for killing certain forms of the Rife pleomorphic organism but strains of even these forms are as low as 2003 and as high as 2012 around the 2007 number, and if you do not treat at exactly the right frequency within 1 hertz, you can wipe out 2007 strains, for example, and still have living 2003 strains or 2012 strains remaining causing further promotion of malignancy.

Furthermore, treating at the Crane numbers does not eliminate the organism. Other forms at other frequencies remain, and the 2007 and 2127 forms keep on growing back. If you do not knock out all forms simultaneously, the organism simply regrows.

Recently, British scientists did DNA sequencing of the Rife pleomorphic organism. As a result, I was able to precisely identify frequencies of Bacillus licheniformis through microscopic photos. These frequencies have been added to the set because I have found that they are helpful for people know to be infected with the Rife organism.

After determining what was required to knock out all forms of the organism on many different people, I developed the numbers posted below which are in hertz, not megahertz. And you must treat +/- 6 hertz around this numbers.

Finally, my experiments indicate that the 11.7 megahertz frequencies, actually as low as 11.3MHZ and as high as 11.9MHZ are frequencies that interact with cellullar mitosis and cause cell death. These frequencies appear to be unrelated to the Rife BX/BY organisms. If they are precisely identified and treated, they appear to knock out malignant cell target populations. Unfortunately, cancer is a multistage phenomenon and there may be large masses of premalignant cells spawning small populations of malignant cells. Each malignant population has a slightly different frequency. It is helpful to knock out these populations as they appear but that does not “cure” cancer. The underlying premalignant cell populations must be dealt with and this usually means alteration of life style, diet, and other factors.

I use frequencies in the literature only as suggestions. Sometimes they work, more often they don’t. Organisms evolve and change, or have multiple forms, causing different frequencies to be required. You must know a lot more than you read to be effective with Rife devices. You must be able to test whether the frequencies you apply knock out the organisms you are targeting.

Many people do not get repeatable, predictable results with Rife technologies. In this endeavor, as in anything else in life, you must know exactly what you are doing and develop skill at it. Most people have unpredictable golf scores but we do not attribute that to the golf clubs they are using and we do not say that golf clubs don’t work for playing golf. Furthermore, getting new golf clubs usually doesn’t solve the problem of your golf game.

In the frequency domain you must:

1. Have a biological model of the organisms you are targeting with frequency devices. Chronic diseases are most often caused by interactions of multiple persistent organisms. All must be targeted simultaneously as they are mutually reinforcing.

2. Have a clinical protocol that precisely targets the relevant organisms with exact frequencies determined for the specific persons and organisms. Treatment times must be appropriate and power transfer must occur at the right level for affected target organ systems. Repeated treatment may be necessary for success.

We all wish we could turn to a manual and run a few “Rife” frequencies to cure a chronic condition that has taken us 20 years to develop, but it is simply not that easy. Becoming a Tiger Woods takes a lifetime of practice and an innate skill that is granted to few of us. Even playing at par takes a huge amount of work and dedication.

FSCAN FAQ: Identifying and Eliminating the “Cancer Germ” Bacillus Licheniformis


The Rife “filterable bacteria” has been studied by the Rife research community for decades and eliminated from many cancer patients using frequency devices of many types. The original frequencies identified by Rife’s colleagues are allegedly: BX form: 21275, BY form: 20080, B Coli filt virus: 17220, B Coli rod form: 8020.

The BX and BY frequencies are believed to have been altered by John Crane to 2127 and 2008 in later years to meet either restrictions on frequency broadcasting or to adjust to limitations of inexpensive frequency devices. This is no longer necessary for either reason and is a historical artifact. In my own experiments, 2127 and 2008 work well as do 21275 and 20080. Both seem to work better together. I have also identified the frequencies 1765 and 2663 as essential in several human and animal tumors. I have assumed that 2663 is the fungus-like form of the bacillus and that 1765 represents a fourth form which must be eliminated or all forms reappear.

So it was with some interest that I examined the Milton Wainwright micrograph in the previous posting. Using the Cameron Aurometer technique which (discussed in an earlier posting), I can often identify a frequency of an organism. In this case, it was clear to me that it was 21554. Testing in the 2663 range, I identified an additional frequency for this organism of 2655. These are good starting points for automated analysis of resonant frequencies of a living organism using the DIRP function of the FSCAN. And both of them were close to previously identified frequencies for forms of this organism.

By chance, I had just eliminated a basal cell carcinoma using a combination of frequency and herbal treatments. The tumor was thoroughly treated for the 1765, 2127, 2008, and 2663 forms of the virus and the FSCAN DIRP function indicated no resonant organisms remained. However, I was concerned about recurrence so immediately checked and the Aurameter tested positive at 21554 and 2655. Running a DIRP scan I got what I initially thought to be a perfect snapshot of the frequency response of the fungal form of Bacillus lincheniformis shown above. After looking at the graph, an FSCAN user reminded me that this was an area of the frequency spectrum where everyone got a lot of hits, possibly from ionic resonance or some other artifact.

Nevertheless, I initially did some sweeps from 2640 to 2670 and 21550 to 21570 using plate zapping of organs that tested positive with the Cameron Aurameter. This strategy seems to reduce the resonance of the region enough to use the Aurameter to pick out four frequencies 2654 2659 21556 21567 where it persistently tested positive. I suspect these may remaining strains of the organism.

I find it best to treat using the following loop based on a modified form of the Turf template. My tests indicate that a square wave, positive DC offset is important to get a positive effect. The F155 programmable frequency generater puts out 5V which is enough to use as a pad device. Lower voltage is not effective and higher is better. The FSCAN will put out up to 27V in this range. I use the F155 to drive an EM5C+ Rife device and a BioPhoton Integrator. The BioPhoton Integrator (described in earlier postings) is effective independent of voltage output and is my primary mode of treatment. I let the loop run until I can no longer detect any resonance.

label start
dwell 5 #I like short dwell times that cycle through frequencies
duty 10 #A square wave run at 10% duty cycle generates even harmonics which are critical with fungus type organisms
pulse 64 75 #Layering a 64HZ wave on top of the primary frequency enhances effectiveness
2654 2659 21556 21567
goto start #Return to start and do again

This program is only for the fungal form of the organism. The other forms must be eliminated also (2127, 2008, and possibly a frequency near 1765). My experiments suggest that Bacillus licheniformis is a mutagen and tumor promoter. If it is not eliminated, more tumors will appear and current tumors will progress to more malignant cellular populations. As a result, I believe that eliminating this organism in healthy people may be one of the best cancer prevention programs available.

Eliminating the organism does not seem to eliminate currently malignant cellular populations. This must be done with frequencies in the 11.7MHZ range in combination with the immune system or lower octaves of the exact frequency in that range which will be different for each cellular population. Since finding the exact frequency may be problematic, some have proposed scanning broad regions in this frequency band. There is research in the literature that suggests that some frequencies selectively inhibit mitosis of malignant cells.

A strong immune system is critically important and may make the difference in success or failure in these experiments. My tests indicate that Transfer Factor Plus is the best available and I would not be without it. Nutritional strategies known to affect tumors and homeopathy can support healing when frequencies alone will not do the job.

Finally, this organism goes systemic like candida. You may need to use plate zapping with microscopic slides of most organ tissue to completely eliminate it. Parasite and candida infections often work in concert to suppress the immune system, helping it to persist. Multiple infections may need to be eliminated concurrently.

Happy hunting, and remember, this is a science experiment, not necessarily a cure for cancer. Check your results with your physician. In this case, nothing remained but some scar tissue which I had biopsied by a dermatologist. The pathology report diagnosis: Scar suggestive of prior procedure or trauma at this site. There is no evidence of basal cell carcinoma.