Rife-SADIE Project menu:
Overview and Introduction
Motivation
Rife Machines 2002-2004
Letter to Rife Forum and introduction to Marlene’s case
Data and conclusions from Marlene’s case
SADIE Research Instrumentation Under Development
NI Hardware based Rife-SADIE Instrumentation
Overview and Introduction
The Rife-SADIE project is centered around a frequency diagnostic and therapeutic device or group of devices based on the pioneering work of Royal Raymond Rife for the treatment of disease correlated to or caused by pathogenic microorganisms.
Click here to read more about Raymond Rife.
An important mission of BEST Solutions is to provide a link back to the original Rife equipment of the mid 20th Century. This will allow independent researchers the ability to test and evaluate the original technology. Using the original technology as a starting point and standard, newer Rife type technology can then be compared, rated and evaluated. BEST Solutions is an engineering resource that can be used by those who wish to openly bring this technology into mainstream science and medicine. BEST Solutions can help provide the test equipment, protocols, test procedures and data handling programs to minimize the Rife researcher’s tasks. It is suggested that those researchers and users, who can openly share their results, do so through an independent information source, such as the Rife Forum, in Europe at www.rifeforum.com.
The Rife Research, Europe website at www.rife.de is one of the best websites currently available documenting the history of Royal Raymond Rife and his inventions as well as continuing work by current researchers using Rife technology. Included are about a dozen short films with fascinating footage showing Rife, his laboratory, microscopes and ray machine killing microorganisms under a microscope: www.rife.de/rife_related_videos.html and www.rife.de/rife_crane_video.html.
Motivation
I personally became involved in Rife Technology in 2002 when my sister in-law was diagnosed with late stage pancreatic cancer. I had previously read Barry Lynes book, The Cancer Cure That Work! Fifty Years of Suppression, and I was fascinated by the story of Royal Raymond Rife. I went to the first ever Rife Conference held in the United States in Las Vegas, in March 2002. While there, I heard so many conflicting stories about which vendor’s machines worked or not, that I didn’t feel comfortable about spending thousands of dollars more on equipment that might or might not work. However, I came away impressed by the vacuum tube model of the AZ-58 displayed there and by the excellent presentation by the British Rife Society on the reverse engineered 1939 Beam Ray device recently discovered in a doctor’s office closet in California. When I got back home I decided to build the 1939 version since it was the most detailed design documented. However, with long lead times on some of the parts, I started to build the AZ-58 in parallel, finding that unit’s parts easier to obtain. This was a trial and error pursuit for me, since my background is in more modern electro-medical equipment, and not RF communications type equipment. My secondary objective, was and still is to validate or not, Aubrey Scoon’s theory that impedance matching and maximum power transfer were far more important than frequency, since each model instrument designed under Rife’s tutelage used a different set of frequencies. I got the 1958 unit (AZ-58) working first, took it to my sister-in-law, and ran the device, slowly dialing through frequencies between about 1900 to 2100 Hertz. I had Kathy call out whenever she had a reaction in her body. She called out when I hit seven of the fourteen frequencies in the Rife Technology Inc. Operations Manual for the Photon Resonant Light Emission System, CARCINOMA – GROUP TWO frequency list including 2128 Hertz, Rife’s frequency for carcinoma using the AZ-58. I didn’t realize this until after I had dialed through all of the frequencies and then matched the frequencies to that protocol. My brother gave her the full treatment the next day and she did have a significant Herxheimer effect over the next three days. However, she was still in the middle of a chemo treatment and decided to wait until that was finished. Also by this time she was in pretty bad shape, maybe more so from 6 months of chemo, than the pancreatic cancer, and she died about two weeks later. I believed that if I had the AZ-58 at the start of the year, that she might well be alive today.
Personally, I had a red-purple lesion growing on the middle of my back for over 5 years. I always thought it was some form of cancer waiting to take off. So I used the AZ-58 with the Scoon Booster and my Heathkit audio frequency generator set for a sine wave of 2128 Hertz, the primary AZ-58 frequency for carcinoma, for three minutes five days in a row, and now it is gone. In five days this lesion that I had growing on my bag scabbed up, grew smaller daily and fell of completely by day five.
Rife Machines 2002-2004
Below are a sample of the Rife Frequency machines I built between 2002 and 2004.
Figure 1: ’39 Audio Osc, 8″ Phanotron, ’39 RF Osc, AZ-58 RF Osc, AZ-58 SSS RF Osc, Scoon Booster Amp
Figure 2: ’39 Audio Osc, 8″ Phanotron, ’39 RF Osc, AZ-58 RF Osc, AZ-58 SSS RF Osc, Scoon Booster Amp, Ultimate B-3 Func Gen, 4″ HH Phanotron
Figure 3: 4″ HH Phanotron, AZ-58 RF Osc, ’39 Audio Osc
Figure 4: AZ-58 RF Osc, 4″ HH Phanotron
Figure 5: AZ-58 RF Osc, 4″ HH Phanotron
Figure 6: AZ-58 RF Osc
Figure 7: AZ-58 RF Osc, 4″ HH Phanotron
The phanotron tube in Figure 7 is hanging at a height that would be about 10 inches above a body lying in bed. This was the system I used on my sister-in-law, Kathy with the pancreatic cancer, as well as on the lesion that had been growing on my back.
We also started experimenting with blood samples/smears after treatment to see if we could identify cellular debris from microorganism or cancer cell kill off. My brother and I both exposed ourselves to the Rife Ray before exposing Kathy. Our blood samples looked clear, while Kathy’s blood samples showed small black particles surrounding the blood cells.
Figure 8: Kathy’s blood smear about an hour after Rife Treatment.
We thought the small dark specks may be evidence of cellular debris from the cancer kill off. Later we used an evaluation copy of NI Vision, with my NI Tech Rep’s help to count cells and particle debris. I believe NI Vision could be very helpful in quantifying the amount of kill off of pathogens and tumor cells.
Below is a Rife-Bare Instrument that is driving the small hand held phanotron tube laying on the wooden box rather than the long tube held in the wooden cradle. This is the type of machine used to kill microorganisms in the videos show on www.rife.de/rife_related_videos.html: “Rife-Bare Plasma Experiment Destroys Organisms” and “Rife-Bare Experiment Destroys Microorganisms”.
Figure 9: Rife-Bare unit operating a mini Hand Held Phanotron Tube
Letter to Rife Forum and introduction to Marlene’s case
In 2003 I began working with a University Professor of Nursing/Colonel Army Reserves, who had ovarian cancer, after her doctors had given up and gave her little chance of surviving the year. On April 2, 2006 I posted these results on the Rife Forum in Europe, www.rifeforum.com.
Hello Everybody,
I thought I would add my two cents worth on the subject “Can a Rife machine cure cancer?”
I have been working with a friend with advanced stage ovarian cancer almost 3 years now and we have tried a number of different Rife units on the market with little success and in some cases detrimental effects (where the cancer dramatically increased). In particular, we tried a unit called Magnaphase, that had been identified as curing lung cancer in one patient, but dramatically increased the ovarian cancer of my friend.
Analyzing the signal from the Magnaphase, I found that there was a ringing of frequencies through 17.034 MHz (17 meter wavelength), the setting of the 1934 device used to treat carcinoma during the very successful clinic held in La Jolla, CA in the summer of 1934. I suspect that there was enough power to destroy cancer in the lungs (being much easier to penetrate), but not down in the heavy organ area, where my friend’s ovarian tumors thrived. If you don’t get enough power at the right frequency to the tumor, you end up stimulating the cancer into growing more, rather than killing it, just as Rife said.
My friend also tried the Rife Bare device from RTI up in Canada and the Bluelight unit from Ed Heft, but found greater response from a functional replica of the AZ-58 I built based on the schematics from the www.rife.org website. We also tried working with the ICOM-718 transmitter sending a modulation frequency in via the ProCom function generator received with the RTI Rife-Bare unit, also to no avail. We worked at 11.78MHz, 17.034 MHz and 1.604 MHz carrier frequencies.
That first year we worked together (2003), we did get some tumor reduction, but a calcium deposit from prior kill off seemed to start covering and protecting the tumor. And so the tumor continued growing, substantially increasing when we tried the Magnaphase device.
I got into this research at the beginning of 2002 when my sister-in-law was diagnosed with pancreatic cancer. She passed away in six months in a most tragic way, as many of you probably know. But in that six months I learned enough about Royal Raymond Rife to know that some of the most important discoveries in medical science were achieved and then lost due to the ignorance, corruption and/or greed of a few.
By the time my sister-in-law passed in July 2003, I was convinced that we must figure out how the 1934 machine worked that successfully cured 16 of 16 advanced stage incurable cancer patients in several months time. I vowed at that time to continue this work until we as a community have rediscovered this technology. I do this in memory of Kathy Berger, my beloved sister-in-law.
Information on super-regeneration can still be obtained from the American Radio Relay League website by obtaining the QST VIEW CD’s for 1915-1929 @ $39.95. A series of articles from the August to December 1922 issues of the QST Magazine explain super-regeneration. The new Rife History document on www.rife.org and the Rife Forum is an excellent effort by AAA Productions to describe a possible scenario for the evolution of Rife Technology from the 1930′s through the 1950′s. However, my money is on the 1934 device and not the 1935 (Rife No. 4) device. I am not a Hoyland fan at all.
Several years ago I started building a vacuum tube super-regeneration system that could allow me to get into the frequency range of the 1934 unit; however, several months into the design I had a brainstorm one night just before falling asleep, that perhaps I could simulate super-regeneration in software more easily. So I have temporarily put the completely hardware version of a super-regenerator on hold.
I did my programming in LabVIEW software (National Instruments being the largest Test & Measurement specific company in the USA), which I use extensively as an Electrical Engineer (working in the medical electronics industry over 25 years). I started with the “Carol” cancer frequency research paper found on www.electroherbalism.com. I came up with a protocol based on that research paper. To simulate super-regeneration, I would build complex harmonic rich waveforms based on the cancer audio MORs used in the 1950′s. The harmonic rich waveforms were built up with from 5 to 60 harmonics. In October I finally came across Dr. Jim Bare’s paper “Understanding Our Frequencies Through Harmonic Associations”. Likewise I built up protocols based on Jim’s paper using anywhere from 5 to 50 harmonic waveforms for at least the cancer frequencies.
From Jul 2005 to Jan 2006 we got decrease’s in my friend’s CA-125 cancer antigen marker, from the low 900′s to the low 500′s. Note that she was also doing chemo. However, she was doing the same chemo without any improvements whatsoever, before we started these protocol’s last July.
After seeing the Bedini pages in December, I got some new ideas myself. I had been amplifying my modulation frequencies from my LabVIEW program/ Data Acquisition Board in my computer with my version of Aubrey Scoon’s Booster Amplifier, but I was trying to keep the amplitude down to not over modulate. It then dawned on me that I needed to get more power to possibly penetrate the calcium deposit layer that seemed to protect the cancer still within the tumor. It seemed that we were able to kill the cancer outside the tumor but not within, since we hadn’t had tumor reduction in over two years.
I found I could increase the input peak to peak voltage into the Scoon Booster amplifier by almost 4 times (to 2.5 Vpp input) without degrading my complex harmonic waveforms for super regeneration simulation. I was now getting out of the Scoon booster amp an 80 Volt peak to peak waveform to modulate the RF carrier in the AZ-58 via the grid of the 812 transmitting tube. We tried sub-harmonic and harmonic carrier frequencies based on both the 1934 (Rife No. 3) and 1935 (Rife No. 4) units. She felt the greatest effect at 4.26 MHz (the 4th sub-harmonic of 17.034 MHz) and less effect at 3.2 MHz (the 2nd harmonic of 1.604 MHz). I also added a gate frequency at this time to further simulate super-regeneration, where the grid circuit is turned off half a cycle. Using a 1000 V probe to measure that output at my phanotron tube resulted in an off scale reading on my oscilloscope > 8000 Volts peak to peak suggesting that super-regeneration might actually be taking place with this setup.
Since January we have had sporadic increases in CA-125 cancer anti-gen marker tests; however at the last doctor’s exam, the doctor was able to feel the back side of the tumor and for the first time in years instead of the gritty hardness of the calcium deposit, he felt the smooth soft tissue of the layer formerly beneath. There was also evidence of a depression in the tumor (hopefully indicating kill off).
My friend Marlene’s niece is a massage therapist, and she also began palpating the tumor trying to break up the calcium wall.
Over a couple month period, Marlene had been doing blood smears at time intervals between treatments. An hour after a light treatment we see numerous big particles of tissue. Eight hours after the treatment, there appears to be muddy looking rivlets within the smear, that I wonder whether might be the tissue debris being broken down by the white cells. Sixteen hours in the number of big particles has decreased and the blood starts clearing up again. So this I believe is the Herxheimer effect as seen in the blood.
I pray that this continues and that we are close to rediscovering the Rife Effect observed during the 1934 cancer clinic. I thank for my courageous friend Marlene, who five years after late diagnosis of ovarian cancer, is still not on any pain meds, and God willing will she her first grandchild born this summer.
May God bless you all in your search for truth, health and happiness.
Jim Berger (Revised slightly grammatically for readability.)
Data and conclusions from Marlene’s case
Figure 10: Frequency Protocol based on “Understanding Our Frequencies Through Harmonic Associations” by James E. Bare, D.C. copyright 2005
Figure 11: Frequency Protocol on “Taking the Mystery Out of the CAFL” by Carol @ OurLifeHouse.com as posted on Electroherbalism.com
Figure 12: Carcinoma Spread +/-1% in 3 Hertz increments
Figure 13: Carcinoma Protocol with Increasing Harmonic Content
Figure 14: Example of Generation of Complex Waveforms with High Amplitude
Harmonic Content Third Step in Protocol – Fundamental with 15 Harmonics
Figure 15: Procedure Report Generation Input
Marlene, Ovarian Cancer approx 5 years after diagnosis
Treatment on AZ-58 Semi-Solid State RF Generator, Scoon Audio Frequency Booster Amp, Computer w/LabVIEW software/National Instruments Data Acquisition Board, Super-Regeneration Simulation software, Bill Cheb 5” hand-held phanatron tube
Figure 16A: Typical Blood Smear photos 1 hour after treatment (Marlene–ovarian cancer)
Figure 16B: Typical Blood Smear photos 1 hour after treatment (Marlene – ovarian cancer)
Figure 17A: Typical Blood Smear photos 8 hours after treatment (Marlene–ovarian cancer)
Figure 17B: Typical Blood Smear photos 8 hours after treatment (Marlene–ovarian cancer)
Figure 18A: Typical Blood Smear photos 16 hours after treatment (Marlene–ovarian cancer)
Figure 18B: Typical Blood Smear photos 16 hours after treatment (Marlene–ovarian cancer)
In summary, Marlene came to me for help with her cancer in the Spring of 2003 after her doctors gave up on her. Marlene wanted to be able to make it through one more Christmas. We were told by all other Rife researchers that once a person has been chemo’d or radiated, that the Rife Ray would not help. Marlene passed away in late January of 2007. The summer before her doctor’s performed an operation in her abdominal area and claimed they had never seen so much dead cancer in a living person during their career. Marlene lived 4 more years making it through 4 more Christmas’ before she passed away. She was able to see her first grand son born in 2006. In hospice when I last saw here in January 2007, she said that in her over 6 year fight with cancer, conventional treatment did not help at all. All gain she made was attributed to the Rife Light, better nutrition and the use of herbs. She encouraged me to continue with this work as long as I could.
Now with seven years behind me in building mainly vacuum tube Rife Instruments, I am now ready to build a completely solid state device. In addition, I plan to develop a feedback diagnostic system to give the doctor or caregiver and patient real time feedback related to the effective of treatment. Therapeutic feedback and diagnosis will be the primary function of the SADIE Instrument.
SADIE Research Instrumentation Under Development
The current SADIE (Subtle Energy Administration & Interpretation of Human Electromagnetics) Prototype Instrumentation in Development consists of a Laptop Computer with a National Instruments (NI) Data Acquisition Card (DAQCard) inserted into the laptop computer’s PCMCIA slot, National Instruments LabVIEW software for measurement and analysis, LabVIEW Advanced Signal Processing Toolkit, DIAdem – Interactive Data Analysis and Report Generation Software, custom bio-amplifier, special measurement, and cable interconnect boards, and medical isolation power sources or batteries. Reference the SADIE Instrument Block Diagram.
SADIE BioAmp Boards 1 and 2 are identical and allow two subjects to be tested simultaneously, with up to 8 differential measurements per subject, or if just one subject up to 16 differential measurements. The bio-amp boards connect back to an interconnect board for further routing by a 20 foot ribbon cable to each board. The boards are small enough to fit into a standard portable CD player carrying case that can be conveniently strapped to the subject’s waist or hung from a shoulder strap.
Standard snap-on ECG leadwires with banana plug terminations plug into the front end of the board. Initial tests will be performed with standard ECG or Stress Test type disposable electrodes.
Each bio-amp board has eight differential input bio-amplifier circuits. At the front end of each bio-amp, a 499k ohm resistor is in place to limit any fault current back to the subject to about 30 microamps. Texas Instrument/Burr Brown (TI/BB) OPA2604 OpAmps configured as unity gain high input impedance buffers feed the differential signal into a TI/BB INA128 Instrumentation Amplifier set for a gain of approximately 100 and connected such that the common mode signal can be sent back to the subject if so selected, similar to the Right Leg (RL) drive common on many electrocardiogram instruments. The amplified signal from the instrumentation amplifier is then fed into a 2 pole Sallen-Key low pass Butterworth response type anti-aliasing filter with the 3 dB cutoff frequency set for 20 kHz, to promote accurate digital processing by the DAQCard.
The common mode voltage from each of the 8 instrumentation amplifier inputs is fed into a TI/BB MPC508 Multiplexer. The 8 amplifiers are typically read in succession and the software is programmed to select and feedback the currently read instrumentation amplifier’s common mode signal to the right leg or another chosen feedback point on the subject’s body. The feedback signal is 180 degrees out of phase with the original signal to cancel out the common mode voltage of the differential measurement, such that the differential voltage can more clearly be read. Typically only the Electrode 10+ (and not the Electrode 10-) is connected back to the subject’s body. A 499k ohm resistor is in line with the Electrode 10+ lead to limit the current back to the subject to 30 microamperes.
The final circuit on the bio-amp board output to Electrode 9+ allows the researcher to inject various signals into the body. With the NI DAQCard-6062E, any waveform with a frequency 0 to 50k Hz (50,000 cycles/second) can be created. Some studies I will personally conduct on myself, will be to chart the frequency response of the various branches or channels of the acupuncture-meridian system. For a normal body impedance of about 1 M ohm (1,000,00 ohms) I can adjust the voltage from 0 to about 3 V peak to peak. Also if any 2 electrodes breach the skin’s resistance, which can drastically drop the body’s resistance from 1 M ohm down to about 500 ohms the maximum current will be limited to about 10 microamperes by the 1M ohm in series with 499k ohm resistors since the typical board voltage will be +/-15 VDC by medically isolated power supply or +/- 12 VDC if operated by batteries.
The National Instruments DAQCard-6062E fits into one of the PCMCIA buss slots of my COMPAQ Presario 3000 laptop computer. This DAQCard can read up to 16 single-ended or 8 differential signals. Note that the SADIE bio-amp boards convert a total of 16 differential signals into 16 single-ended signals while amplifying the signal by 100 times. The DAQCard-6062E has a maximum sampling rate of 500,000 (500k) Samples per second. To resolve a complex waveform you need to sample the waveform at least at 10 equally time spaced points along the waveform and preferably at 20 points. This means that if I am reading just one channel I can distinguish waveforms at frequencies up to 50kHz fairly good and up to 25kHz very good. If I am looking at 2 channels, for instance 1 set of electrodes reading the differential signal from front to rear of the body in the area of the heart charka of the healer and make the same measurement with the 2nd bio-amp board on the healee, I could read the 2 waveforms almost simultaneously at frequencies up to 25kHz fairly well and up to 12.5kHz very well. What this means is that we can read one channel each on 2 subjects with fairly good resolution (12 bit analog to digital conversion) well within the range of frequencies measured by Dr. Valerie Hunt, and documented in her book “Infinite Mind”. By similar calculation, if we wish to read all 16 channels close to simultaneously, we can read 50kHz/16 = 3.125kHz waveforms fairly well and 25kHz/16 = 1.56kHz waveforms very well. According to Dr. Hunt’s work, the first level of the human energy field was in the 200 to 1.2kHz range. Therefore to measure higher levels of the human energy field we must limit our tests points or read two channels successively at time when all possible electrodes are being monitored (missing data while other channels are read).
The 8 digital input/output (DIO) lines of the DAQCard are used as digital outputs to programmatically select the correct instrumentation amplifier’s common mode voltage to feedback to the subject.
The 2 DAQCard analog outputs are used to drive the 9th electrode terminals via a voltage controlled current waveform (limited to 10 microamperes maximum) at frequencies up to 50kHz. A question I have pondered over the past few years, is whether I can chart the frequency response of the acupuncture-meridian energy channels. Are there medically significant differences in the frequency response and signal amplitude for a given input signal when comparing healthy and diseased subjects? Can I measure blockages in the energy channels that correlate to the location of a cancerous tumor? Can I more effectively carry a frequency at the mortal oscillitory rate of the cancer and kill the microorganism that may be the cause or at least a symptom of the disease? The ideas? Just keep coming.
Referring back to the SADIE Instrument Block Diagram, there is additional circuitry above and below the NI DAQCard-6062E block on the diagram. A rotary switch is used for each bio-amp board to select one channel at a time to further amplify the signal, filter out as much 60 hertz noise from the environment as possible, and then send the signal to an audio stereo amplifier with two speakers to play back in real time the electrical activity from the human body or 2 bodies at once when connected. Dr. Valerie Hunt claims to be the first to record the music of the charkas and the human energy field. We will attempt similar recordings with the SADIE Instrument.
There is a second switch for the 8th channel of each bio-amp board to do other types of measurement. In the upper right hand corner of the block diagram, is a circuit I am hoping will allow us to read photon emission from a subject. I have some type 931A, 931B (visible light spectrum) and 1P28 (visible and ultraviolet light spectrum) photomultiplier tubes. If the light is measureable, I also have various colored filters from which we could possibly distinguish specific colors. Then with the help of an independent person capable of reading auras (as did Rosalyn Bruyere for Dr. Valerie Hunt’s experiments) we can determine if there is any correlation between the instrument’s readings and the aura readings. Note that the photomultiplier tube socket converts 15Volts DC to -1250 Volts DC to drive the tube. This circuit is isolated from the other circuitry by using a separate medically isolated power supply and a TI/BB ISO124 Isolation Amplifier to safely send the output signal back to the computer for processing.
The lower circuit that can be switched in on the second bio-amp board is a magnetometer with 2 each magnetically opposed 80,000 turn coils mounted on a ferrite rod. Calculations show that I could possibly measure magnetic fields in the pico-tesla (10^-12) range, and therefore the magnetic field of the heart. The magnetically induced current in the coils is amplified by a TI/BB INA128 instrumentation amplifier and then sent through a 60 Hz notch filter to eliminate as much 60 Hz noise as possible before sending the signal back to the laptop computer for further processing. As an alternative, until I figure out how to wind the coils properly, I can connect in an F.W. Bell Model 5080 Gauss/Teslameter, that will allow me to read down to the nano-Tesla (10^-9) range.
Figure 19: SADIE Instrument, First Prototype
Once I saw how many wires were involved, it became obvious that the setup would be far too restrictive for the patient, so I put this part of the project on hold until I could afford wireless technology.
Work is proceeding on a Graphical User Interface with a blue man and blue women to help locate primary measurement points on the body.
Figure 20: Blue Man GUI
Figure 21: Blue Woman GUI
Every different type of tissue in the human body has a unique frequency. In addition, every organ of the body has a unique frequency based on its size and shape. The SADIE device’s primary function will be to measure whether the frequencies of the patient are in a normal range and if not to therapeutically deliver a frequency from the Rife Ray Tube or a SADIE transducer to stimulate the organ and tissue back to its normal limits after the Rife treatment is used to kill off the targeted pathogen. The SADIE GUI will have the ability to look at Blue Man and Blue Woman from six different views: front, back, right side, left side, top of head and bottom of feet. Contacting any single acupuncture point on the body will bring into view the point identification, the organ it is connected to and the work that can be accomplished at that point.
NI Hardware based Rife-SADIE Instrumentation
With the approval of this Medical Device Grant Application and the use of state of the art National Instruments hardware and software, I believe that I can reduce development time and time to market by three to four times on this project. With LabVIEW Real-Time oe Embedded and FPGA, some of the more complex custom hardware can be replaced by software and off the shelf hardware from NI. See Figure 22 below.
Figure 22: Rife-SADIE Instrumentation
The NI single board Real Time Computer (sbRIO-9632 or similar) would be the brains of the system storing all unique pathogen characteristics in memory. Based on the pathogen characteristics and diseased tissue characteristics also stored in memory, optimal gate, carrier and modulation frequencies will be generated and appropriately combined to create a state of the art frequency treatment. An LCD touchscreen display module will provide the user interface. A custom printed circuit board assembly will convert the computer output into the driving voltage for the phanotron plasma tube. The phantron tube is held approximately 10 inches above the body and directed toward the diseased organ(s) of the subject’s body. Based on Rife’s records for treating cancer, a recommended treatment time is 3 minutes every 3 days. An NI WLS-9234 wireless Dynamic Signal Analyzer using electronic stethoscope(s) or other sensors, and/or an NI WLS-9205 data acquisition board mated to a bio-amps board and electrodes could provide feedback related to the treatment.
The full blown system could be used at the doctor’s office or hospital once every week or two. Blood samples could be taken and analyzed during office or hospital visits to measure the treatment effectiveness. A small more compact version of just the therapy portion of the device could be made for home use between doctor visits for use by the patient.
Over the past 12 years a DNA researcher named Charlene Boehm (www.dnafrequencies.com) has explored the work of Royal Rife and other researchers, in particular studying DNA and RNA of pathogens in humans, animals and plants. Based on the length of a pathogen’s DNA (bacteria) or RNA (virus), and the tissue electrical and magnetic characteristics, the most optimal frequencies needed to kill a particular pathogen are determined. Details on the cellular properties and mathematics involved are defined on her website. Charlene Boehm has identified the DNA or RNA frequencies for over 240 human, 125 animal and 25 plant pathogen based disease’s. Included in her work are the DNA or RNA frequencies of pathogen’s related to 30 forms of human cancer. She will continue to add new frequencies upon request. For each disease, she defines the pathogen involved and references the medical/scientific document that confirms the pathogens relationship to the disease. She offers the information both for commercial and non-commercial use at reasonable cost after signing an appropriate agreement on use. I will be using Charlene Boehm’s services.
In addition there is an open sharing site on frequencies, where literally hundreds of manufacturer’s and users share frequencies that worked for them for literally hundreds of different pathogens and diseases. The lists are located here.