RIFE RESEARCH - Natural Therapy Center

FUTURE RESEARCH PROJECT (Strictly Confidential)

INTRODUCTION

Royal Raymond Rife (1888 – 1971) was one of the medical geniuses of this century – a scientist, pathologist and microbiologist who developed an optical microscope (Universal Microscope) that could provide magnifications and resolutions that defied the laws of optics and physics. He was able, through special quartz optics and a creative optical heterodyning techniques, to obtain these resolutions even though they surpassed the theoretical limits of ordinary visible light microscopy. His most powerful instrument is said to be the Universal Microscope, which had a magnification of 61,000X and a resolution of 30,000 diameters.

Dr Rife’s history and experiments and results are far too extensive to cover here as the objective is to focus on future research that can achieve the same results that Rife had, using modern technology that Rife did not have access to in his day. There are links provided below that will provide a lot more information on Rife’s achievements throughout his long research career.

Rife’s Universal Microscope

Rife began his work with the microscopes in the early 1920’s and it was from these original developments that he would make many of his revolutionary discoveries. It is argued that Rife was the first person to empirically prove that virus and bacteria are pleomorphic forms. Pleomorphism is the phenomenon by which one distinct life form mutates into another.

Rife basically classified pathogenic bacteria into 10 individual groups. Rife demonstrated that any organism within its group could be transformed morphologically into any other organism within the 10 groups by carefully altering the media or pH in which it was cultured. Of course this discovery tends to contradict modern microbiology which teaches that a bacteria’s morphology is fixed and unchangeable.

By 1920, Royal Rife had finished building the world’s first high magnification microscope with which life viruses could be seen. By 1933, he had perfected that technology and had constructed the incredibly complex Universal Microscope, which had nearly 6,000 different parts and was capable of magnifying objects 60,000 times their normal size! With this incredible microscope, Rife became the first human to actually see a live virus, and until quite recently, the Universal Microscope was the only one which was able view live viruses.

Modern electron microscopes (which can go up to 1,000,000 x) instantly kill everything beneath them, viewing only the mummified remains and debris. What the Dr. Rife microscope can see is the bustling activity of living viruses as they change form to accommodate changes in environment, replicate rapidly in response to carcinogens, and transform normal cells into tumour cells.

Objectives of Research

The research study proposed here will basically revisit a lot of Dr Rife’s work, using equivalent modern-day microscopes capable of similar magnifications and resolutions, as well as frequency generators capable of producing similar frequencies to Dr Rife’s original generators.

The microscope that is now commercially available is known as the SeeNano Pro – this has the ability to see living viruses up to a magnification of about 30,000 times, with a resolution of 100 nm or lower. This will enable the researchers to see the living viruses they are studying and be able to determine their Mortal Oscillatory Rate (MOR) much like Dr Rife did more than 75 years ago. These microscopes were developed by a brilliant German scientist called Olbrich and one of the initial protypes that he developed known as the Ergonom 500 is also still available for purchase as I saw it a couple of years ago when I specifically travelled to Germany to discuss things with the IP rights owner, an electrical engineer who worked with Olbrich for over 20 years and bought the rights after Olbrich retired. The Ergonom 500 was being sold for 225,000 Euros at the time, fully modified to bring up to date with modern electronics.

SeeNano Pro Microscope

PROJECT FOCUS

The project will focus on two main aspects of research, much like Dr Rife did so many years ago:

1. Identifying the Mortal Oscillatory Rate (MOR) of a number of pathogens causing infectious diseases globally – MOR is the frequency that will destroy the pathogens.

2. Isolating and identifying the Mortal Oscillatory Rate (MOR) of a number of pleomorphic cancer-causing viruses

3. Identifying the MOR for a line of different cancer cell lines.

Initially, the project will focus on some of the more common pathogens that are life-threatening, but no treatments have been found to date. These include, but will not be restricted to: MRSA (Methicillin-resistant Staphylococcus aureus), Hepatitis B and C, Human Papilloma Virus (HPV), Herpes Simplex 1 and 2, and possibly Malaria. Other bacterial infections that are seeing a comeback such as Tuberculosis (TB) and Cholera, as well as pneumonia, strep throat and Meningitis.

Commercialising this technology and making it freely available can help to save many hundreds of thousands of lives all over the globe.

SPECIFIC RESEARCH INTERESTS

The most serious concern with antibiotic resistance is that some bacteria have become resistant to almost all of the easily available antibiotics. These bacteria are able to cause serious disease and this is a major public health problem.

In 2013, CDC published a report outlining the top 18 drug-resistant threats to the United States. These threats were categorised based on level of concern: urgent, serious, and concerning.

It is envisaged that as soon as funding is in place this important research will begin by identifying the Mortal Oscillatory Rates or the specific oscillatory frequencies that will eradicate infectious diseases, beginning with the urgent categories such as:

Methicillin-Resistant Staphylococcus aureus (MRSA)

Methicillin-Resistant Staphylococcus Aureus (MRSA) causes a range of illnesses, from skin and wound infections to pneumonia and bloodstream infections that can cause sepsis and death. Staph bacteria, including MRSA, are one of the most common causes of healthcare-associated infections and deaths and is of particular concern in the modern world.

Clostridium Difficile (CDIFF)

Clostridium difficile (C. difficile) causes life-threatening diarrhoea. These infections mostly occur in people who have had both recent medical care and antibiotics. Often, C. difficile infections occur in hospitalized or recently hospitalized patients.

Update: A 2015 CDC study found that C. difficile caused almost half a million infections among patients in the United States in a single year. An estimated 15,000 deaths are directly attributable to C. difficile infections, making it a substantial cause of infectious disease death in the United States. We estimate that up to $3,800,000,000 in medical costs could be saved over 5 years.

Carbapenem-Resistant Enterobacteriaceae (CRE)

Untreatable and hard-to-treat infections from carbapenem-resistant Enterobacteriaceae (CRE) bacteria are on the rise among patients in medical facilities. CRE have become resistant to all or nearly all the antibiotics we have today. Almost half of hospital patients who get bloodstream infections from CRE bacteria die from the infection.

Drug-Resistant Neisseria Gonorrhoeae

Neisseria gonorrhoeae causes gonorrhea, a sexually transmitted disease that can result in discharge and inflammation at the urethra, cervix, pharynx, or rectum.

In addition to these antibiotic resistant strains of bacteria, there are other infectious diseases that presently have no cure using any form of medication, which include:

Hepatitis C

Hepatitis C is a liver disease caused by the hepatitis C virus: the virus can cause both acute and chronic hepatitis infection, ranging in severity from a mild illness lasting a few weeks to a serious, lifelong illness. 130–150 million people globally have chronic hepatitis C infection and approximately 500 000 people die each year from hepatitis C-related liver diseases. There is currently no vaccine for hepatitis C.

Human Papilloma Virus (HPV)

Human papilloma viruses are known as HPV. They can affect the skin and the moist membranes that line parts of the body, including: the lining of the mouth and throat, the vulva, the cervix, the vagina and the anus.

There are many different species of HPV, and the HPV-16 and HPV-18 are the “high risk” that can cause cervical cancer in women, for which there is no real cure apart from surgery.

COMMERCIALISATION OF THE SCIENTIFIC RESULTS

Once the Mortal Oscillatory Rates are identified for these microorganisms, then frequency or bioresonance devices can be made commercially available and accessible to people around the globe.

There are two different types of frequency devices that can be manufactured:

Large devices that can be used in clinics and hospitals to treat a large group of people concomitantly.
Small, hand-held bioresonance devices that can be used in the comfort of ones home, with individual SIM cards encoded with the frequencies that will eradicate specific microorganisms. So the users will simply purchase in addition to the main device the SIM card they want to use, i.e. MRSA, HPV and the like.

The technology to build such devices is presently available, but first the Mortal Oscillatory Frequencies must be discovered through the research that is being proposed here.

In the long term, this will empower each person to treat themselves of life-threatening infectious diseases, without the side effects of medications in a much more cost effective way for themselves and the state as a whole. This will save the hospital and the state millions in funds that are presently spent on treating these diseases, as well as millions of deaths globally.

Cancers

Dr Royal Raymond Rife in 1934 had identified the Bacillus X and Y viruses that he found in all cancer cells that he examined. After identifying the Mortal Oscillatory Rate or the oscillatory frequency that kills this virus, he was able to successfully cure a number of cancer cases.

There is no reason why this work should not be revisited and the frequencies identified to eradicate these cancer viruses, which inevitably have mutated and changed frequencies over the last 80 years or so.

FURTHER READING

VIDEOS TO WATCH

The Ray of Discovery – Dr Royal Raymond Rife – Part 1

The Ray of Discovery – Dr Royal Raymond Rife – Part 2

The Ray of Discovery – Dr Royal Raymond Rife – Part 3

The Ray of Discovery – Dr Royal Raymond Rife – Part 4

The Ray of Discovery – Dr Royal Raymond Rife – Part 5

The Ray of Discovery – Dr Royal Raymond Rife – Part 6

Resonance – Beings of Frequency (Documentary)

The Rife Research Labs – Part 1

The Rife Research Labs – Part 2

The Rife Research Labs – Part 3

The Rife Research Labs – Part 4

The Rife Research Labs – Part 5

The Suppressed Cancer Cure – Dr Rife

BUDGET PLAN – 2016 – 2017

The project is planned to span over two years and can then be expanded to include other pathogens that have not been identified during this initial stage of the research, given that the research infrastructure will be in place.

The basic expenses for set-up and running costs include:

Setting up a modern microbiology lab with the following equipment:

SeeNano Pro microscope – will allow one to see living pathogens, including viruses to a 100 nm true resolution enabling magnification greater than 25,000 times and much higher, using electronic magnification, fully equipped with video cameras for recording the research.

The current Grayfield Lens System (GLS) is the result of over 40 years of research and development. It is a unique optical system whereby the limits normally associated with optical resolution simply do not apply. The results are similar to what Dr. Rife achieved many years ago.

Culture Growth Chamber – allows the researcher to observe living cultures in real time at high resolutions. It is possible to grow cultures in these chambers and observe the effects of hitting the pathogens in vitro with frequencies.

Nano Positioning System – this system has been specifically designed to allow the exact positioning of an object with incredible accuracy to 2.5 nm.

TOTAL: €275,000

Other laboratory equipment includes:

ECO Clean bench
2 x Microbiological incubators
2 x Biological safety cabinets – Class II and III
Water Purification System
Dual-Action Orbital Reciprocating Shaker
Micro-Ultracentrifuge
2 x Sterilizers
Various Glassware
Rife Frequency Generators
Spectrum Analyzer
Frequency counter

TOTAL: €75,000

3.1 Purchasing of consumables, chemicals, living microorganisms

£15,000 yearly x 2 =

TOTAL: €30,000

4.1 Renting appropriate premises for setting up the laboratory – approximately 100 sq. m divided into different sections – preferably away from cities.

TOTAL: €25,000 yearly x 2 =

TOTAL: €50,000

5.1 Re-structuring the rented space with electrics, appropriate wall coverings, clean room etc.

TOTAL: €35,000

6.1 Installation of computer terminals with a central database system and backups

TOTAL: €5,000

7.1 Installation of Fireproof filing cabinets and safe

TOTAL: €5,000

8.1 Installation of security alarm and monitoring and surveillance equipment

TOTAL: €8,000

9.1 Fire, building and equipment insurance

£5,000 yearly x 2 =

TOTAL: €10,000

10.1 Yearly servicing contract for laboratory equipment

€8,000 x 2 =

TOTAL: €16,000

11.1 Yearly commodities such as electricity, water, gas (laboratory rooms must maintain even temperatures all year round)

€18,000 yearly over two years =

TOTAL: €36,000

12.1 Salaries of scientists and staff members:

1 Prinicipal Investigator – €90,000 + National Insurance (N.I) + Income tax (I.T)

1 Qualified post-doctoral Clinical Microbiologist – €75,000 + N.I. + I.T.

1 microbiological laboratory technician – €30,000 + N.I. + I.T.

1 secretary/administrative director – €24,000 + N.I. + I.T.

1 cleaning staff (part-time) – €10,000 + N.I. + I.T.

TOTAL YEARLY SALARIES: €230,000

TOTAL OVER TWO YEARS: €460,000

13.1 Yearly travelling expenses for research purposes, including hotels and transport for researchers.

TOTAL: €15,000

14.1 A 20% contingency budget to cover any time extensions, additional equipment and staff not presently included in the abovementioned figures:

€200,000

GRAND TOTAL OVER TWO YEARS: €1,220,000

N.B. These figures are realistic estimates and cannot be precise at the moment of preparation due to fluctuating exchange rates, freight charges as well as efficient and cost effective sourcing of equipment and materials.

A factoring of plus/minus 10% would make this more accurate.

DR GEORGIOU – A BRIEF BIOGRAPHY

This link will give further information on Dr Georgiou’s career to date

QUESTIONS AND ANSWERS FROM VARIOUS INVESTORS/PHILANTHROPISTS

Are you concerned about your personal safety… in pursuing this?

ONLY WE, THE RESEARCHERS AND THE INVESTORS WILL KNOW – WHEN RESULTS ARE OBTAINED THEN CAREFUL PLANNING IS REQUIRED BEFORE THEIR RELEASE. I AM AWARE OF THE DANGERS, BUT NOT AFRAID OR OVERLY CONCERNED ABOUT MY SAFETY.

2. My understanding… is that the suppression of this technology extends worldwide… not just in the U.S.

IT IS TRUE, EVEN THOUGH THERE ARE A NUMBER OF RESEARCH CENTERS THAT ARE WORKING IN THE FIELD OF FREQUENCIES FOR HEALTH AND THE FDA IS A LOT MORE OPEN-MINDED REGARDING THESE INSTRUMENTS THAN THEY WERE IN R’S DAYS. I WOULD NOT SAY THAT ALL FREQUENCY INSTRUMENTS AVAILABLE HAVE BEEN SUPPRESSED OR ARE BEING HOUNDED BY MEDICAL ASSOCIATIONS AND FDA – WE HAVE COME A LONG WAY SINCE R’S DAYS AND IN OUR DAYS THERE IS AN AWAKENING WITH MORE PEOPLE DEMANDING THEIR RIGHT TO GOOD, NON-INVASIVE HEALTH CARE

3. Is there one particular disease you could cure… where you would encounter the least resistance from these suppressors… in getting it out into the world ?

THE PHARMACEUTICAL COMPANIES HAVE DECLARED THAT THEY ARE NOT INVESTING FURTHER IN DEVELOPING ANTIBIOTICS FOR MRSA AND OTHER ANTI-BIOTIC RESISTANT BUGS THAT ARE KILLING MANY PEOPLE WORLDWIDE (https://www.pharmaceutical-journal.com/news-and-analysis/features/why-are-there-so-few-antibiotics-in-the-research-and-development-pipeline/11130209.article?firstPass=false). THEY KNOW THAT THEY CAN INVEST HALF A BILLION IN RELEASING A NEW ANTIBIOTIC, ONLY TO FIND THAT WITHIN A COUPLE OF YEARS IT NO LONGER WORKS AS NEW BUGS HAVE MUTATED THAT ARE RESISTANT TO IT – IT IS NO LONGER COST EFFECTIVE FOR THEM (https://www.forbes.com/sites/quora/2017/08/18/why-pharmaceutical-companies-arent-in-a-rush-to-address-increasing-antibiotic-resistance/#b04a6304d3a2).

SO, WORKING WITH THESE ANTIBIOTIC RESISTANT MICROORGANISMS WOULD BE WELCOME BY MOST SCIENTIFIC CIRCLES AROUND THE WORLD. IN ADDITION, MANY OTHER INFECTIOUS DISEASES THAT CANNOT BE CURED WITH DRUGS AND KILLING MILLIONS AROUND THE GLOBE ANNUALLY. CANCER CAN RUN IN PARALLEL WITH ALL OF THESE EXPERIMENTS, BUT PERHAPS FINDING THE RESONANT FREQUENCIES OF MACROPHAGES WHICH GOBBLE UP CANCER CELLS WOULD BE ANOTHER NOVEL WAY OF APPROACHING THE CANCER ISSUE (I AM ALREADY WORKING ON A SUPPLEMENT FORMULATION THAT WILL BE AVAILABLE IN THE NEXT COUPLE OF MONTHS TO DO THIS) – WE CAN STUDY MACROPHAGES UNDER THE MICROSCOPE IN REAL TIME, AS WELL AS OTHER IMMUNE COMPONENTS THAT ARE IMPORTANT IN ERADICATING CANCER.

4. What is the environment like in Cyprus ???

IT IS FAIRLY SAFE TO CONDUCT THESE EXPERIMENTS IN A PRIVATE LAB AND MAYBE TAP INTO SOME OF THE UNIVERSITIES IF OTHER SPECIAL EQUIPMENT IS REQUIRED, WITHOUT THEM KNOWING THE BIGGER PICTURE. HAVING BEEN HERE FOR 35 YEARS NOW, I ALSO “KNOW” A LOT OF PEOPLE, SO SHOULD BE FINE – MUCH SAFER HERE THAN THE USA AND OTHER COUNTRIES!

5. Would you have the this lab on your 3 acre property where the Da Vinci Center is?

IT IS 4.5 ACRES ACTUALLY – IT IS PROBABLY THE SAFEST PLACE AS THERE IS ALWAYS SOMEONE HERE AND I AM AROUND THE COMPLEX ALMOST 24-HOURS PER DAY AS I HAVE A LOT OF PROJECTS RUNNING ON THIS COMPLEX. WE WILL HAVE CAMERAS AND ALARMS AND OTHER SECURITY FEATURES ONCE EQUIPMENT IS INSTALLED IN MY EXISTING LABORATORY. WE ALSO HAVE UP TO 200 SQUARE METERS OF LAB SPACE POTENTIALLY AVAILABLE TO EXPAND INTO – AT PRESENT MY LAB IS ONLY TAKING UP 50 SQUARE METERS. ONCE COMPLETED, THIS LAB WILL BE FORT KNOX AND AWAY FROM PASSERS-BY AS WE ARE IN THE COUNTRY ABOUT 6 MILES FROM THE TOWN CENTER. BECAUSE OF THE EXISTING INFRASTRUCTURE WE CAN BE UP AND RUNNING IN A COUPLE OF WEEKS ONCE FUNDING AND EQUIPMENT IS IN PLACE.

6. Do you have any doubt whatsoever about your ability to successfully recreate this?

I HAVE STUDIED AND BEEN EXPERIMENTING WITH THIS FOR A COUPLE OF DECADES NOW – I ALSO REGISTERED FOR A PHD IN R TECHNOLOGY AT A PRESTIGIOUS UK UNIVERSITY AND BEGAN THIS RESEARCH BUT COULD NOT COMPLETE IT AS I WAS SELF-FINANCED AND COULD NOT MOVE THE RESEARCH ON WITHOUT SOME SERIOUS FUNDING WHICH I DID NOT HAVE. I HAVE ALSO BEEN EXPERIMENTING WITH BIORESONANCE TECHNOLOGIES FOR ABOUT 20 YEARS NOW, SO HAVE A LOT OF EXPERIENCE IN THIS FIELD. I HAVE ALSO WRITTEN COLLEGE COURSES FOR ENERGY MEDICINE AND BIORESONANCE AND TEACH THE SUBJECT TO OTHER PRACTITIONERS, INCLUDING CLINICAL PRACTICUMS. IT IS RARE TO FIND A BIOLOGIST SCIENTIST WHO IS ALSO ATUNE TO ENERGY MEDICINE. I BELIEVE THAT THERE ARE MANY POSSIBILITIES FOR HEALTH AND DISEASE USING BIORESONANCE DEVICES THAT ARE PROPERLY TUNED WITH THE CORRECT FREQUENCIES – MOST DISEASES SHOULD BE ABLE TO BE CURED WHEN ONE PUTS THEIR MIND TO IT. I ALSO STRONGLY BELIEVE THAT ENERGY MEDICINE AND BIORESONANCE IS GOING TO BE THE MEDICINE OF THE FUTURE AND I WOULD LOVE TO BE ONE OF ITS PIONEERS.

I ALSO HAVE A CYMASCOPE IN MY LAB WHICH MAKES SOUND AND FREQUENCY VISIBLE – THIS OPENS UP ANOTHER WORLD AS IT IS ALSO POSSIBLE TO TAKE SIGNALS FROM CELL MEMBRANES USING RAMON MICROSCOPY AND SEE THEIR MORPHOLOGICAL SIGNAL ON THE CYMASCOPE – COMPARING NORMAL CELLS WITH CANCER CELLS – SEE https://www.youtube.com/watch?v=OfPNLfSrHoM

I AM NOT INTERESTED IN HOARDING MORE MONEY AT MY AGE – THIS IS NOT WHAT MOTIVATES ME – BUT I WOULD LOVE TO LEAVE A LEGACY BEHIND ME AND MAKE DR R SMILE FROM HIS GRAVE! WITH THE RIGHT PEOPLE AND FINANCING WE SHOULD BE ABLE TO MOVE FORWARD SWIFTLY WITHOUT THE NEED TO GO BACK TO THE DRAWING BOARD AS MOST OF THIS BACKGROUND WORK HAS ALREADY BEEN DONE.

CERTAINLY AS FAR AS THE ELECTRONIC SIDE OF THINGS IS CONCERNED, AS YOU WILL SEE FROM THE FIXED LINK OR THE ATTACHMENT, THIS HAS NOW BEEN PERFECTED WAY BEYOND WHAT R COULD HAVE DONE BACK IN HIS DAYS WITH THE ELECTRONICS THAT WERE AVAILABLE. I HAVE SOURCES WHERE THIS HIGHLY DEVELOPED BIORESONANCE EQUIPMENT CAN BE PURCHASED AND USED IN THE LAB – I ALREADY HAVE THESE DEVICES INSTALLED IN MY EXISTING LAB AND THEY WORK FINE.

QUESTION SET 2 – 06.02.19

For this 2-year research study… are you planning on starting a brand-new company… with a new name, completely independent of The Da Vinci Center?

YES, IT WOULD PROBABLY BE A GOOD IDEA, BUT WOULD NEED TO DISCUSS WITH MY LAWYER TO SEE HOW THIS WILL BE STRUCTURED. A CERTAIN POSSIBILITY THAT WOULD PROBABLY HAVE ADVANTAGES FOR THE INVESTOR (S), INCLUDING CYPRIOT CITIZENSHIP.

Would all products manufactured from this proposed 2 year research be under the umbrella of this same new company name? Or, do you plan to create a new company… for each new product created?

NOT CERTAIN, AGAIN WOULD NEED TO DISCUSS WITH MY LAWYER BUT IT IS AGAIN A POSSIBILITY – ANYTHING THAT WORKS BEST LEGALLY, TAX WISE ETC WOULD BE FEASIBLE.

You mention manufacturing a small portable device, with interchangeable SIM cards to treat multiple diseases… fantastic!

YES – THIS IS A GOOD IDEA AS THE CUSTOMERS COULD KEEP RETURNING TO ORDER MORE AND MORE SIM CARDS AFTER THEY HAVE BOUGHT THE MAIN DEVICE. WE WOULD NEED TO FIND A WAY OF “LOCKING” THE FREQUENCIES ON THESE SIM CARDS SO THEY CANNOT BE DECIPHERED.

How many different diseases could this one device treat?

AS MANY AS WE WANT, DEPENDING ON THE MOR’S THAT WE HAVE IDENTIFIED FOR THE VARIOUS PATHOGENS STUDIED. EACH SIM CARD CAN HAVE ITS OWN FREQUENCY, SO PEOPLE CAN PURCHASE A SIM CARD FOR EACH PATHOGEN OR DISEASE. THERE IS NO REASON WHY THESE PORTABLE DEVICES COULD NOT BE USED FOR TREATING COMMON SORE THROATS FROM STREP INFECTIONS, SINUSES, HEADACHES AND MORE. A TRUE “FAMILY DOCTOR”!

Would it be possible to use an already existing hand held device such as the DETA ELIS

or other brand of portable device, and create new SIM cards for this device, or simply set this device to the correct desired frequency, or frequencies… and still be able to effectively treat various diseases?

YES, I HAVE A GOOD RELATIONSHIP WITH DETA ELIS, AND WE COULD DISCUSS THE POSSIBILITIES, BUT THE RUSSIANS ARE VERY POSSESSIVE OF THEIR PRODUCTS AND INVENTIONS, SO MAY BE DIFFICULT TO FORM BRIDGES HERE FOR MUTUAL COOPERATION.

HOWEVER, THESE DEVICES ARE EASY TO BUILD AND GET MANUFACTURED IN ASIAN COUNTRIES – ONCE WE KNOW WHAT WE WANT, THIS IS THE EASY PART OF THE COMMERCIALISATION OF THE RESULTS.

THE DETA ELIS DEVICES ARE QUITE WEAK IN POWER GENERALLY – 1 WATT – SO MAYBE NOT SUITABLE FOR OUR NEEDS. THE DETA ELIS COMPANY HAVE SENT ME DEVICES WITH AN EXTERNAL ANTENNA FOR TESTING, SO WOULD BE GOOD TO FACTOR THIS INTO THE EXPERIMENTS ONCE LAB IS UP AND RUNNING. MY FEELING IS THAT WE WOULD NEED TO INCREASE THE POWER OUTPUT, BUT STILL KEEP THE DEVICES SMALL.

Would these small portable devices be able to penetrate human tissue enough, to cure the intended disease, or are they limited to being able to only go so deep, therefore making them not fully effective?

THIS ALL DEPENDS ON THE POWER OUTPUT, AS WELL AS THE SPECIFIC MOR’S ELICITED FROM THE RESEARCH. THE MORE POWER, THE BIGGER THE DEVICE.

The original machines could be tuned to a specific frequency that the user wanted to output or they could output two frequencies simultaneously which would produce other frequencies known as side band frequencies… which to my understanding the side band frequencies can act like a “sweep” of sorts if one of these frequencies did not kill the organism another nearby one would… is that correct?

YES, THIS IS PARTLY CORRECT – BUT IT WAS THE RICH HARMONICS PRODUCED BY THE IONISING GAS THAT R USED, BASED ON A CARRIER FREQUENCY OF 3.1 MHZ MODULATED BY THE SPECIFIC MOR.

IN TODAY’S WORLD, WITH THE ELECTRONICS THAT WE PRESENTLY HAVE, WE CAN FEED EIGHT DIFFERENT FREQUENCIES INTO THE PLASMA TUBE SIMULTANEOUSLY, NOT ONLY TWO. THIS CAN GREATLY REDUCE TREATMENT TIMES. AT THE END OF THE DAY, IT IS THE CORRECT MOR’S (MORTAL OSCILLATORY RATES) THAT WILL DO THE WORK, AND THESE ARE THE ONES THAT NEED TO BE FOUND BY EXPERIMENTATION.

IN ADDITION, THE FREQUENCY GENERATORS THAT WE USE TODAY ARE CAPABLE OF SWEEPING ACROSS A WIDE BAND OF FREQUENCIES, AS WELL AS CHANGING THEIR WAVE FORMS AND MORE. THERE ARE A LOT OF EXPERIMENTAL POSSIBILITIES TO LOOK AT, BUT WE WILL STAY AS CLOSE TO R’S WORK AS POSSIBLE – HE LEFT ENOUGH INFORMATION TO HELP US IN THE REPLICATION OF HIS WORK.

GIVEN THAT MORE THAN 80 YEARS HAVE PASSED SINCE R WAS IDENTIFYING THE MOR’S FOR THE PATHOGENS HE WAS WORKING WITH, THESE SAME PATHOGENS HAVE NOW MUTATED SO WILL HAVE DIFFERENT MOR’S – THIS IS WHY IT IS IMPORTANT TO REVISIT HIS WORK, EVEN THOUGH THE MOR’S ARE NOT GOING TO BE VERY FAR OFF WHAT HE FOUND, BUT PRECISION IS IMPORTANT.

The original one large vacuum tube seemed to add something for the frequency treatment… is there anything to this?

R USED EXISTING X-RAY TUBES THAT WERE AVAILABLE IN HIS DAYS. THESE TUBES ARE NOW REPRODUCED TO THE EXACT SPECS AS R USED WITH HIS ORIGINAL X-RAY TUBE – I HAVE ONE IN MY LAB. THESE ARE AVAILABLE TO ORDER. THERE ARE OTHER TUBES THAT CAN ALSO BE USED – THESE, HOWEVER, NEED TO BE TUNED TO THE SPECIFIC FREQUENCY GENERATOR BEING USED.

Would a correct frequency for one particular disease work on all people? Or, would this frequency have to be adjusted or customized to work for each individual?

AS OUR CELLS, TISSUES AND ORGANS ARE THE SAME IN EACH SPECIES, THEN THIS WOULD WORK FOR ALL HUMANS WITHOUT THE NEED FOR INDIVIDUAL TUNING, UNLESS THERE ARE GROSS ANATOMICAL DIFFERENCES.

Is there any way to Patent any of this new research you wish to complete? How do you plan on protecting this one and half million-dollar investment from imitation and copycats? Is there any way to patent any part of the handheld devices you wish to manufacture? How are you planning on protecting these devices from imitation and copycats?

YES, ONE CAN PATENT THE RESEARCH METHODOLOGY AND ITS RESULTS. THE PROBLEM WITH PATENTS IS THAT THE INFORMATION BECOMES PUBLICLY AVAILABLE AFTER THE PATENT IS ISSUED. THE CHINESE LOVE THIS! IT MAY BE BEST TO KEEP THIS PROPRIETARY – NO ONE NEEDS TO KNOW THE SPECIFIC FREQUENCIES USED, AND THERE ARE WAYS TO “MASK” THE FREQUENCIES IN THE FIELD OF ELECTRONICS SO THAT THEY ARE NOT EASILY DECIPHERED. WE WOULD NEED THE INPUT OF A GOOD BROADCAST ENGINEER – WE HAVE SUCH A PERSON IN LARNACA JUST A FEW MILES FROM ME.

As you know… there are now many R machines and frequencies being sold. Are all of these nothing more than guesswork, having been unable to verify… through actual live observation… the pathogen’s current M.O.R.?

MOST OF THESE DEVICES ARE NOT WORKING ON THE SAME FREQUENCIES THAT R USED IN HIS CLINICAL R-RAY INSTRUMENT. THEY ARE WORKING ON HARMONIC FREQUENCIES, AND MANY ARE WORKING ON THE CRANE FREQUENCIES. CRANE WAS AN ENGINEER WHO WORKED WITH R BUT DEVELOPED A DIFFERENT BREED OF INSTRUMENTS THAT WERE NO WHERE NEAR AS EFFECTIVE AS R’S INSTRUMENTS. THESE CRANE FREQUENCIES ARE STILL USED IN A LOT OF THESE CHEAP SOLID-STATE INSTRUMENTS THAT ARE BEING SOLD ON THE INTERNET.

MANY OF THEM WORK IN THE KILOHERTZ RANGE, NOT THE MEGAHERTZ RANGE THAT R’S INSTRUMENTS WERE WORKING AT, PARTICULARLY FOR ERADICATING THE BX AND BY VIRUSES IDENTIFIED IN CANCER CELLS.

THE EXPERIMENTAL AMPLITUDE MODULATION DEVICE THAT I HAVE IN MY LAB WORKS UP TO 20 MHZ WHICH IS EVEN BEYOND THE FREQUENCY RANGE THAT R WORKED WITH.

How would we know, or find out… if there wasn’t someone else right now working on this same project… since the microscope has been available since 2017?

I AM IN TOUCH WITH A NUMBER OF R RESEARCHERS AND HAVE OCCASIONAL CONVERSATIONS – THERE IS NO ONE THAT I AM AWARE OF THAT IS WORKING IN THIS FIELD. ONE MAJOR PROBLEM IS TO MARRY THE PHYSICS WITH THE BIOLOGY AS YOU WILL FIND MANY ELECTRONIC ENGINEERS WORKING ON PERFECTING THE ELECTRONICS, BUT VERY FEW, IF AT ALL BIOLOGISTS WHO CAN MARRY THE ELECTRONICS AND PHYSICS WITH THE BIOLOGICAL RESEARCH.

THE OTHER PROBLEM IS THE FINANCING – IT IS EXPENSIVE TO START FROM SCRATCH AND BRING IN ALL THE EXPERTISE REQUIRED – WOULD REQUIRE MANY MILLIONS. IT IS REALLY A NON-STARTER IF YOU CANNOT HAVE THE MICROSCOPE IN PLACE, BUT ALSO THE LAB SETUP WITH SAFETY CABINETS AND THE LIKE, INCLUDING RENTING SPACE AND HIRING STAFF – THIS IS BEYOND THE BUDGET OF THE AVERAGE SCIENTIST INTERESTED IN THIS KIND OF RESEARCH.

Is there a way to find out the actual sales from the microscope company? Are they still the only microscope company in the world with a microscope that can see the M.O.R.?

IT IS DIFFICULT TO BE PRECISE IN HOW MANY MICROSCOPES LIKE THE ERGONOM THAT THEY HAVE ACTUALLY SOLD, BUT WHEN I SPENT 3 DAYS IN GERMANY WITH THE MAIN ENGINEER WITH THE IP RIGHTS FOR THESE MICROSCOPES, WORKING THROUGH THE DETAILS OF BUILDING SUCH A MICROSCOPE, IT EMERGED THAT THERE PROBABLY ARE NOT MORE THAN 5-6 OF THESE EXPENSIVE MICROSCOPES THAT HAVE BEEN SOLD.

WHAT MAKES THESE MICROSCOPES SPECIAL IS THEIR HIGH RESOLUTION AND MAGNIFICATION, ENABLING THEM TO SEE VIRUSES, NOT ONLY BACTERIA IN THEIR LIVING FORM. SCANNING ELECTRON MICROSCOPES HAVE THIS TYPE OF HIGH RESOLUTION AND MAGNIFICATION, BUT AS THE SAMPLE IS SCATTERED WITH ELECTRONS, IT WILL DIE, SO YOU CANNOT SEE IT IN ITS LIVING STATE.

THERE ARE, HOWEVER, OTHER COMPANIES THAT ARE NOW TRYING TO PRODUCE “SUPER SCOPES” THAT HAVE VERY HIGH RESOLUTION, BUT HAVING SPOKEN TO A COUPLE, THEIR MAIN FOCUS IS IN PRODUCING MICROSCOPES FOR THE ELECTRONIC INDUSTRY AND NOT FOR BIOLOGICAL RESEARCH.

BEFORE PURCHASING THE GERMAN MICROSCOPE, IT WOULD CERTAINLY BE WORTH INVESTIGATING THIS FURTHER AND SEEING WHICH COMPANIES AND RESEARCHERS HAVE PRODUCED SOMETHING IN THE RANGE OF SUPER RESOLUTION. I AM A MEMBER OF THE ROYAL MICROSCOPICAL SOCIETY OF THE UK AND REGULARLY READ THEIR SCIENTIFIC JOURNALS WITH INTEREST IN IDENTIFYING SUCH MICROSCOPES. WE WOULD NEED TO SPEND A LITTLE TIME INVESTIGATING WHAT IS COMMERCIALLY AVAILABLE, EVEN THOUGH THE ERGONOM MICROSCOPE HAS BEEN TRIED AND TESTED BY OLBRICH FOR OVER 4 DECADES AND IS USED FOR BIOLOGICAL SPECIMENS TOO. THERE IS A MEDICAL DOCTOR WHO BOUGHT THE LITTLE BROTHER ERGONOM FROM OLBRICH A NUMBER OF YEARS AGO WHO WE CAN SPEND A DAY OR TWO WITH SEEING HIS WORK AS HE DOES WORK WITH CANCER, BUT NOT WITH FREQUENCIES.

ANOTHER WAY OF SETTING UP THE RESEARCH IS TO USE SWEEPING FREQUENCIES FOR A PATHOGEN AND USE AN ELECTRON MICROSCOPE TO DETERMINE WHETHER THE PATHOGENS HAVE LYSED (BROKEN OPEN DUE TO ELECTROPORATION). A SECOND-HAND ELECTRON MICROSCOPE IS RELATIVELY CHEAP (MAYBE 30 – 40,000 EUROS), SO THIS MAY BE ANOTHER AVENUE ONE CAN PURSUE.

THERE ARE ALSO OTHER BIOLOGICAL MEASURING DEVICES THAT CAN DETERMINE LIVE, VIABLE PATHOGENS, MOSTLY THE SIZE OF BACTERIA AND LARGER, AGAINST THOSE THAT ARE NON-VIABLE OR DEAD. THESE DEVICE ARE LESS THAN 10,000 EUROS TO PURCHASE NEW.

How would you handle the legal issues for people using these devices? Would people be able to treat themselves… or could they only use it in a doctor’s office? Under a doctor’s supervision ?

BOTH. THERE WOULD BE THE SMALLER DEVICES THAT COULD BE USED FOR HOME USE, PURCHASING THE SPECIFIC SIM CARDS REQUIRED. THEN THERE ARE THE LARGER, MORE POWERFUL AND WIDE-RANGING DEVICES THAT CAN BE PURCHASED BY PRACTITIONERS FOR OFFICE OR CLINIC USE.

THERE COULD ALSO BE EVEN LARGER DEVICES RUNNING 6 OR MORE TUBES SIMULTANEOUSLY FOR HOSPITAL WARDS FOR TREATING PATIENTS DYING OF MRSA AND OTHER ANTI-BIOTIC RESISTANT PATHOGENS WHO HAVE REALLY BAD PROGNOSES. THESE LARGER DEVICES COULD BE HOUSED IN A CONTAINER AND SIT PERMANENTLY IN THE MIDDLE OF THE WARD SO THAT PATIENTS CAN SIT AS A GROUP AROUND THE TUBES AND BE TREATED TOGETHER – VERY COST EFFECTIVE. THIS WOULD PROBABLY BE ONE OF THE BIGGEST SELLERS – COULD ALSO BE PURCHASED BY MANY OF THE PRIVATE CLINICS AND USED PREVENTATIVELY.

Do people even need to go to doctor before using the device? Once they find out exactly what disease they have?

YES, IN ORDER TO GET A DIAGNOSIS FOR THE PATHOGEN INVOLVED, UNLESS THEY ALREADY KNOW FROM THE SIGNS AND SYMPTOMS THEY PRESENT WITH.

Even though these devices are completely harmless to healthy human tissue… would a person have the right to use the device on themselves without any legal problems or issues?

YES, THERE ARE MANY ELECTROMAGNETIC DEVICES ON THE MARKET THAT ARE USED FOR WELLNESS – AS LONG AS ONE DOES NOT MAKE CLAIMS. DETA ELIS IS ONE SUCH EXAMPLE.

As compared to another person using the device on them who is not a doctor… would this situation open up a legal can of worms? Does this mean people need to use this exclusively on themselves?

IF THE PERSON BEING TREATED HAS GIVEN THEIR PERMISSION – WRITTEN IS ALWAYS BEST – THEN THERE IS NO REASON WHY THE “TREATING” PERSON SHOULD BE A DOCTOR.

Have you thought of a way to allow people from the U.S. to be able to invest in this… with 100% full legal protection of their money so they can sleep at night… knowing that their money and investment is 100% safe and protected?

UNFORTUNATELY, WITH ANY RESEARCH PROJECT, THERE IS ALWAYS AN ELEMENT OF RISK INVOLVED, SO THERE IS NO 100% FULL LEGAL PROTECTION THAT I CAN THINK OF, IN THE SAME WAY AS THERE WOULD NOT BE WITH ANY INVESTMENT. ALL INVESTMENTS HAVE THEIR RISKS AND REWARDS, AND THE INVESTOR WOULD NEED TO WEIGH THESE UP CAREFULLY. A PHILANTHROPIST WOULD SEE THE LARGER PICTURE OF HELPING HUMANITY AND PERHAPS LEAVING A LEGACY BEHIND THEM, SO THIS QUESTION WOULD BECOME OBSOLETE!

THIS IS WHO R HAD IN HIS RESEARCH TEAM – TIMKEN, FROM TIMKEN BEARINGS, A WEALTHY ENTREPRENEUR OF HIS TIME WHO FELL IN LOVE WITH R’S RESEARCH AND LITERALLY PROVIDED R WITH AN OPEN CHECK – HELPING HIM MOVE HIS RESEARCH FORWARD QUICKLY WITHOUT HAVING TO WORRY ABOUT FINANCES. IT WAS ALSO ONE OF THE BEST EQUIPPED LABS IN THE WORLD AT THE TIME.

Was reading about Cyprus offering full citizenship without having to live in the country… to foreign investors within 6 months. Would your investment qualify for this?

Not certain, but found the following information that may be useful – https://www.prime-property.com/en/page/European-passport-by-investment/?utm_medium=cpc&utm_source=google&utm_term=%2Bcyprus%20%2Bcitizenship

PS Let me know if you are coming to the U. S. I have ideas for letting the people know about this… I can only tell you about in person.

I WILL ONLY COME TO THE USA AFTER FINALISING A PLAN THAT IS IMPLEMENTABLE – I HAVE DONE A LOT OF TRAVELLING IN THE PAST TO MEET UP WITH POTENTIAL INVESTORS ONLY TO FIND THAT NOTHING COMES OF IT. THIS IS QUITE FRUSTRATING AND ENERGY-DRAINING, SO DO NOT WANT TO REPEAT THESE SAME SCENARIOS. WITH MODERN TECHNOLOGY THESE DAYS, WE CAN HAVE AS MANY MEETINGS AS WE LIKE FROM THE COMFORT OF OUR OWN HOMES.

I know it will be hard for you to believe… but nothing like this has ever been done before… and absolute secrecy is of the essence.

I BELIEVE IT ABSOLUTELY AND AGREE WITH THE SECRECY – MUST BE WISE THESE DAYS!

If you are coming to the U.S. I will travel to wherever you are… otherwise we will have to wait until I can travel to your center…which will not be for at least 3 months.

LOOK FORWARD TO MEETING WITH YOU AND YOUR MOTHER IN CYPRUS WHERE YOU CAN ALSO SEE THE SETUP I HAVE AND BEGIN OPTIMIZING YOUR HEALTH WHICH IS IMPORTANT.

I have come to realize that a vastly superior… zero cost… method for letting people know about this… once the research is complete… could be as valuable as the research and discoveries themselves. You would never even have to run a single ad for the public to see.

Please, only publish our questions and your answers on your investor page… nothing else. Thank you.

LOOK FORWARD TO HEARING ABOUT IT SOMETIME – LET ME KNOW WHEN YOU HAVE FOUND A MORE SECURE WAY OF COMMUNICATING.

Dr. George J Georgiou, Ph.D., D.Sc (AM)., N.D., M.Sc., B.Sc., C. Psychol., AFBPsS., C.Biol., M.S.Biol., RMS., FAACS., ABS., ACS., DipION., M.H., AMH., GCRN., MRNI., FBIH., ESLM.
Holistic Medicine Practitioner, Researcher, Author
www.naturaltherapycenter.com
[email protected]
Tel: (+357) 24-82 33 22
Skype: davincicyprus

Dated: 30.01.2019

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FUTURE RESEARCH USING BIORESONANCE BASED ON DR RIFE’S WORK

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