Extracted from the book The Cancer Cure That Worked! by Barry Lynes.
 Marcus Books, PO Box 327, Queensville, Ontario, Canada

Requiem For Royal Rife The Hubbard Interviews - Part One:

Requiem For Royal Rife - Part Two The Hubbard Interviews:

Deconstructing Beam Rays Incorporated Searching For The AMA
By Shawn Montgomery 3-30-7

The history of medicine has always been the history of alternative medicine, for every new idea, every new theory, every new method of healing has come not from within the bastions of conventional medicine, but rather from outside the current convention. Being the hippopotomonstrosity that medicine is and always has been, its members do not like being told how to do their jobs by outsiders nor do they appreciate learning that something might exist beyond the scope of their education, which cost them dearly. Pasteur's idea that germs caused disease was ridiculed for years. Penicillin was actually discovered in the mid 1800's by a medical student, but because he was only a medical student it was written off as a curiosity. Even after its formal discovery, Penicillin sat shelved for years before being tested. Dr Semmelweis committed suicide in a mental institute after years of trying to get physicians to wash their hands after performing autopsies (instead they ran down the hall to deliver a baby and kill the mother). And what about this guy by the name of Lawrence Burton? He wasn't a physician, but rather a scientist. In 1966, under the aegis of the American Cancer Society, he arranged for an audience of 70 scientists and some 200 science writers and performed for them a demonstration using mice with visible tumors. He injected each with a solution and in just 45 minutes the tumors had shrunk 50%. An hour and a half later, the tumors had practically disappeared. Newspapers around the world ran the story of Dr Burton and his cancer cure on their front pages. Eight years later he opened a cancer clinic in New York where, for some cancers, he realized a better than 50% cure rate; higher than any other physician or clinic in America. Two years later, due to pressure from the FDA, he was forced to close his clinic and move his entire operation to the Commonwealth of the Bahamas where today he still has better rates of success with certain cancers, better than any other clinic in America. For the address and phone number, go here: http://www.mnwelldir.org/docs/cancer1/altcan.htm

Of all of these stories about the frustrated efforts of alternative thinking wending its way into mainstream medicine, the most interesting (and most terrifying) is that of Dr Royal Rife. You see, Dr Rife had discovered a very inexpensive means of curing not only cancer, but some of the most dreaded diseases in society today such as the Ebola virus and AIDS. His research was destroyed, his associates harassed and some even killed, and after years of hounding he died of an overdose administered to him in Grossmont Hospital, in San Diego, California.

Rife was probably one of the most brilliant (not to mention persistent) scientists ever to have walked upon this planet. He won 14 awards from the government for his research and was given an honorary medical degree from the University of Heidleberg.

When the technology didn't exist, Rife invented it. Financed by millionaires like Henry Timken, Rife invented the Universal Microscope with 5,682 parts. It was a miraculous machine that could see things smaller than waves of light (which was then and is still today thought to be impossible). Rife was the first to see a live virus. Today's electron microscopes see viruses, but they destroy them in the process through the bombardment of electrons.

While examining bacteria and viruses, Rife noticed that each one gave off a distinct light (or color) pattern. (In the late sixties it was discovered that every living cell actually gives off light and the healthier the cell the healthier the light; conversely the sicker the cell the weaker the light. But this research by Rife was done in the twenties using technology Rife himself invented.) So Rife began to experiment with instruments he invented that oscillated at the frequencies he'd determined from the organisms (bacteria and viruses) and he discovered that by playing back their own pattern of oscillation, slightly modified, he could destroy them without affecting the tissues around them. In other words, Rife could kill a particular virus or bacterium using light rays alone, light rays that were absolutely harmless to the host animal, but deadly to the microbe.

Now comes the really interesting part of Rife's work: he discovered a virus that caused cancer. And he discovered a cure.

Please accept this for a second until I can fill you in on a few things.

There are many possible causes of cancer, from carcinogens to bacteria to viruses to parasites to even forms of light rays not visible to the naked eye. However, to prove that something is a cause of a disease, certain rules must be followed and these rules, originally set out in Koch's Theorem have been slightly modified today. Can there be more than one cause to a disease? Yes, if by following the rules you can prove two or more causes. Today there are those who feel that HIV is not the cause of AIDS simply because HIV has never been proven according to the rules to be the culprit.

Articles TOC

Copyright © 2003
Wellness Directory of Minnesota
Contact us

For non commercial use: You may copy, print, reprint, and/or transfer this entire article, if and only if it is unmodified and in its complete state with this copyright notice attached and all the links work properly. All others must contact us in writing: Contact Us

Reproduced gratefully from: http://www.mnwelldir.org/docs/cancer1/rife.htm

 

Royal Raymond Rife

Edited by Jeff Rense
11-7-2

 

 

 

 

Rife's Universal Virus Microscope #3

 

Imagine, for a moment, that you have spent more than two decades in painfully laborious research-- that you have discovered an incredibly simple, electronic approach to curing literally every disease on the planet caused by viruses and bacteria . Indeed, it is a discovery that would end the pain and suffering of countless millions and change life on Earth forever. Certainly, the medical world would rush to embrace you with every imaginable accolade and financial reward imaginable. You would think so, wouldn't you?

 

Unfortunately, arguably the greatest medical genius in all recorded history suffered a fate literally the opposite of the foregoing logical scenario. In fact, the history of medicine is replete with stories of genius betrayed by backward thought and jealously, but most pathetically, by greed and money.

 

In the nineteenth century, Semmelweiss struggled mightily to convince surgeons that it was a good idea to sterilize their instruments and use sterile surgical procedures. Pasteur was ridiculed for years for his theory that germs could cause disease.

 

Scores of other medical visionaries went through hell for simply challenging the medical status quo of day, including such legends as Roentgen and his X-rays, Morton for promoting the 'absurd' idea of anaesthesia, Harvey for his theory of the circulation of blood, and many others in recent decades including: W.F. Koch, Revici, Burzynski, Naessens, Priore, Livingston-Wheeler, and Hoxsey.

 

Orthodox big-money medicine resents and seeks to neutralize and/or destroy those who challenge its beliefs. Often, the visionary who challenges it pays a heavy price for his 'heresy.'

 

So, you have just discovered a new therapy which can eradicate any microbial disease but, so far, you and your amazing cure aren't very popular. What do you do next? Well, certainly the research foundations and teaching institutions would welcome news of your astounding discovery. Won't they be thrilled to learn you have a cure for the very same diseases they are receiving hundreds of millions of dollars per year to investigate? Maybe not, if it means the end of the gravy train. These people have mortgages to pay and families to support. On second thought, forget the research foundations.

 

Perhaps you should take your discovery to the pharmaceutical industry; certainly it would be of great interest to those protectors of humanity, right? But remember, you have developed a universal cure which makes drugs obsolete, so the pharmaceutical industry just might be less than thrilled to hear about your work. In fact, the big shots might even make it certain that your human disease-ending technology never sees the light of day, by preventing it from becoming licensed by the regulatory agencies.

 

Now, assuming your amazing cure is an electronic instrument, the only cost of using it is electricity. And it is absolutely harmless to patients, who can recover without losing their hair, the family home, and their life savings. So, with your technology, there is no longer any reason for people with cancer to pay over $300,000 per patient -- to become deathly ill from chemotherapy, radiation treatments, and the mutilation of surgery. It sounds like you won't find many friends and support among practicing oncologists, radiologists, and surgeons, doesn't it?

 

You might try the hospitals and big clinics. But how thrilled are they going to be about a therapy administered in any doctor's office; which reverses illness before the patient has to be hospitalized? Thanks to you, the staffs of these institutions will essentially be out of work.

 

Well then, how about the insurance companies? Surely, they would be delighted to save the expense of hospitalization - at least the companies which haven't invested in hospitals, where the staff is now sitting around waiting for someone to break a leg or be in a car accident...and the ones who don't lose policyholders as a result of your invention...and the companies which aren't trying to divest their pharmaceutical stock. Oh well, forget the insurance companies, too.

 

It looks like you just might have a little problem with the medical establishment, no?

 

Probably the only friends you'll have will be the patients and those progressive doctors who see change as an opportunity, rather than a threat to their established money-making monopoly. Those people will love you. But they don't call the shots.

 

What follows, now, is the story of exactly such a sensational therapy and what happened to it. In one of the blackest episodes in recorded history, this remarkable electronic therapy was sabotaged and buried by a ruthless group of men. It has re-emerged in the underground medical/alternative health world only since the mid-80's. This is the story of Royal Raymond Rife and his fabulous discoveries and electronic instruments.

 

If you have never heard of Rife before, prepare to be angered and incredulous at what this great man achieved for all of us only to have it practically driven from the face of the planet. But, reserve your final judgement and decision until after you have read this.

 

Of course, some may regard this as just an amusing piece of fiction. However, for those who are willing to do some investigating on their own, there will be mentioned several highly-respected doctors and medical authorities who worked with Rife as well as some of the remarkable technical aspects of his creation.

 

However, in the final analysis, the only real way to determine if such a revolutionary therapy exists is to experience it yourself. The medical literature is full of rigged 'double-blind' clinical research tests, the results of which are often determined in advance by the vested corporate interests involved.

 

If FDA and other regulatory and licensing procedures and guidelines are observed, it is your privilege to experiment with this harmless therapy. So let's now turn to the story of the most amazing medical pioneer of our century.

 

Royal Raymond Rife was a brilliant scientist born in 1888 and died in 1971. After studying at Johns Hopkins, Rife developed technology which is still commonly used today in the fields of optics, electronics, radiochemistry, biochemistry, ballistics, and aviation. It is a fair statement that Rife practically developed bioelectric medicine himself.

 

He received 14 major awards and honors and was given an honorary Doctorate by the University of Heidelberg for his work. During the 66 years that Rife spent designing and building medical instruments, he worked for Zeiss Optics, the U.S. Government, and several private benefactors. Most notable was millionaire Henry Timkin, of Timkin roller bearing fame.

 

Because Rife was self-educated in so many different fields, he intuitively looked for his answers in areas beyond the rigid scientific structure of his day. He had mastered so many different disciplines that he literally had, at his intellectual disposal, the skills and knowledge of an entire team of scientists and technicians from a number of different scientific fields. So, whenever new technology was needed to perform a new task, Rife simply invented and then built it himself.

 

Rife's inventions include a heterodyning ultraviolet microscope, a micro-dissector, and a micro-manipulator. When you thoroughly understand Rife's achievements, you may well decide that he has the most gifted, versatile, scientific mind in human history.

 

By 1920, Rife had finished building the world's first virus microscope. 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 being 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 instantly kill everything beneath them, viewing only the mummified remains and debris. What the 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 tumor cells.

 

But how was Rife able to accomplish this, in an age when electronics and medicine were still just evolving? Here are a few technical details to placate the skeptics...

 

Rife painstakingly identified the individual spectroscopic signature of each microbe, using a slit spectroscope attachment. Then, he slowly rotated block quartz prisms to focus light of a single wavelength upon the microorganism he was examining. This wavelength was selected because it resonated with the spectroscopic signature frequency of the microbe based on the now-established fact that every molecule oscillates at its own distinct frequency.

 

The atoms that come together to form a molecule are held together in that molecular configuration with a covalent energy bond which both emits and absorbs its own specific electromagnetic frequency. No two species of molecule have the same electromagnetic oscillations or energetic signature. Resonance amplifies light in the same way two ocean waves intensify each other when they merge together.

 

The result of using a resonant wavelength is that micro-organisms which are invisible in white light suddenly become visible in a brilliant flash of light when they are exposed to the color frequency that resonates with their own distinct spectroscopic signature. Rife was thus able to see these otherwise invisible organisms and watch them actively invading tissues cultures. Rife's discovery enabled him to view organisms that no one else could see with ordinary microscopes.

 

More than 75% of the organisms Rife could see with his Universal Microscope are only visible with ultra-violet light. But ultraviolet light is outside the range of human vision, it is 'invisible' to us. Rife's brilliance allowed him to overcome this limitation by heterodyning, a technique which became popular in early radio broadcasting. He illuminated the microbe (usually a virus or bacteria) with two different wavelengths of the same ultraviolet light frequency which resonated with the spectral signature of the microbe. These two wavelengths produced interference where they merged. This interference was, in effect, a third, longer wave which fell into the visible portion of the electromagnetic spectrum. This was how Rife made invisible microbes visible without killing them, a feat which today's electron microscopes cannot duplicate.

 

By this time, Rife was so far ahead of his colleagues of the 1930's(!), that they could not comprehend what he was doing without actually traveling to San Diego to Rife's laboratory to look through his Virus Microscope for themselves. And many did exactly that.

 

One was Virginia Livingston. She eventually moved from New Jersey to Rife's Point Loma (San Diego) neighborhood and became a frequent visitor to his lab. Virginia Livingston is now often given the credit for identifying the organism which causes human cancer, beginning with research papers she began publishing in 1948.

 

In reality, Royal Rife had identified the human cancer virus first...in 1920! Rife then made over 20,000 unsuccessful attempts to transform normal cells into tumor cells. He finally succeeded when he irradiated the cancer virus, passed it through a cell-catching ultra-fine porcelain filter, and injected it into lab animals. Not content to prove this virus would cause one tumor, Rife then created 400 tumors in succession from the same culture. He documented everything with film, photographs, and meticulous records. He named the cancer virus 'Cryptocides primordiales.'

 

Virginia Livingston, in her papers, renamed it Progenitor Cryptocides. Royal Rife was never even mentioned in her papers. In fact, Rife seldom got credit for his monumental discoveries. He was a quiet, unassuming scientist, dedicated to expanding his discoveries rather than to ambition, fame, and glory. His distaste for medical politics (which he could afford to ignore thanks to generous trusts set up by private benefactors) left him at a disadvantage later, when powerful forces attacked him. Coupled with the influence of the pharmaceutical industry in purging his papers from medical journals, it is hardly surprising that few heave heard of Rife today.

 

Meanwhile, debate raged between those who had seen viruses changing into different forms beneath Rife's microscopes, and those who had not. Those who condemned without investigation, such as the influential Dr. Thomas Rivers, claimed these forms didn't exist.

 

Because his microscope did not reveal them, Rivers argued that there was "no logical basis for belief in this theory." The same argument is used today in evaluating many other 'alternative' medical treatments; if there is no precedent, then it must not be valid. Nothing can convince a closed mind. Most had never actually looked though the San Diego microscopes...air travel in the 1930's was uncomfortable, primitive, and rather risky. So, the debate about the life cycle of viruses was resolved in favor of those who never saw it (even modern electron microscopes show frozen images, not the life cycle of viruses in process).

 

Nevertheless, many scientists and doctors have since confirmed Rife's discovery of the cancer virus and its pleomorphic nature, using dark field techniques, the Naessens microscope, and laboratory experiments. Rife also worked with the top scientists and doctors of his day who also confirmed or endorsed various areas of his work. They included: E.C. Rosenow, Sr. (longtime Chief of Bacteriology, Mayo Clinic); Arthur Kendall (Director, Northwestern Medical School); Dr. George Dock (internationally-renowned); Alvin Foord (famous pathologist); Rufus Klein-Schmidt (President of USC); R.T. Hamer (Superintendent, Paradise Valley Sanitarium; Dr. Milbank Johnson (Director of the Southern California AMA); Whalen Morrison (Chief Surgeon, Santa Fe Railway); George Fischer (Children's Hospital, N.Y.); Edward Kopps (Metabolic Clinic, La Jolla); Karl Meyer (Hooper Foundation, S.F.); M. Zite (Chicago University); and many others.

 

Rife ignored the debate, preferring to concentrate on refining his method of destroying these tiny killer viruses. He used the same principle to kill them, which made them visible: resonance.

 

By increasing the intensity of a frequency which resonated naturally with these microbes, Rife increased their natural oscillations until they distorted and disintegrated from structural stresses. Rife called this frequency 'the mortal oscillatory rate,' or 'MOR', and it did no harm whatsoever to the surrounding tissues.

 

Today's Rife instruments use harmonics of the frequencies shown on the display screen. The wavelength of the actual frequency shown (770hz, 880hz, etc.) is too long to do the job.

 

This principle can be illustrated by using an intense musical note to shatter a wine glass: the molecules of the glass are already oscillating at some harmonic (multiple) of that musical note; they are in resonance with it. Because everything else has a different resonant frequency, nothing but the glass is destroyed. There are literally hundreds of trillions of different resonant frequencies, and every species and molecule has its very own.

 

It took Rife many years, working 48 hours at a time, until he discovered the frequencies which specifically destroyed herpes, polio, spinal meningitis, tetanus, influenza, and an immense number of other dangerous disease organisms.

 

In 1934, the University of Southern California appointed a Special Medical Research Committee to bring terminal cancer patients from Pasadena County Hospital to Rife's San Diego Laboratory and clinic for treatment. The team included doctors and pathologists assigned to examine the patients - if still alive - in 90 days.

 

After the 90 days of treatment, the Committee concluded that 86.5% of the patients had been completely cured. The treatment was then adjusted and the remaining 13.5% of the patients also responded within the next four weeks. The total recovery rate using Rife's technology was 100%.

 

On November 20, 1931, forty-four of the nation's most respected medical authorities honored Royal Rife with a banquet billed as The End To All Diseases at the Pasadena estate of Dr. Milbank Johnson.

 

But by 1939, almost all of these distinguished doctors and scientists were denying that they had ever met Rife. What happened to make so many brilliant men have complete memory lapses? It seems that news of Rife's miracles with terminal patients had reached other ears. Remember our hypothetical question at the beginning of this report: What would happen if you discovered a cure for everything? You are now about to find out....

 

At first, a token attempt was made to buy out Rife. Morris Fishbein, who had acquired the entire stock of the American Medical Association by 1934, sent an attorney to Rife with 'an offer you can't refuse.' Rife refused. We many never know the exact terms of this offer. But we do know the terms of the offer Fishbein made to Harry Hoxsey for control of his herbal cancer remedy. Fishbein's associates would receive all profits for nine years and Hoxey would receive nothing. Then, if they were satisfied that it worked, Hoxsey would begin to receive 10% of the profits. Hoxsey decided that he would rather continue to make all the profits himself. When Hoxsey turned Fishbein down, Fishbein used his immensely powerfulpolitical connections to have Hoxsey arrested 125 times in a period of 16 months. The charges (based on practice without a license) were always thrown out of court, but the harassment drove Hoxsey insane.

 

But Fishbein must have realized that this strategy would backfire with Rife. First, Rife could not be arrested like Hoxsey for practising without a license. A trial on trumped-up charges would mean that testimony supporting Rife would be introduced by prominent medical authorities working with Rife. And the defense would undoubtedly take the opportunity to introduce evidence such as the 1934 medical study done with USC. The last thing in the world that the pharmaceutical industry wanted was a public trial about a painless therapy that cured 100% of the terminal cancer patients and cost nothing to use but a little electricity. It might give people the idea that they didn't need drugs.

 

And finally, Rife had spent decades accumulating meticulous evidence of his work, including film and stop-motion photographs. No, different tactics were needed...

 

The first incident was the gradual pilfering of components, photographs, film, and written records from Rife's lab. The culprit was never caught.

 

Then, while Rife struggled to reproduce his missing data (in a day when photocopies and computers were not available), someone vandalized his precious virus microscopes. Pieces of the 5,682 piece Universal microscope were stolen. Earlier, an arson fire had destroyed the multi-million dollar Burnett Lab in New Jersey, just as the scientists there were preparing to announce confirmation of Rife's work. But the final blow came later, when police illegally confiscated the remainder of Rife's 50 years of research.

 

Then in 1939, agents of a family which controlled the drug industry assisted Philip Hoyland in a frivolous lawsuit against his own partners in the Beam Ray Corporation. This was the only company manufacturing Rife's frequency instruments (Rife was not a partner). Hoyland lost, but his assisted legal assault had the desired effect: the company was bankrupted by legal expenses. And during the Great Depression, this meant that commercial production of Rife's frequency instruments ceased completely.

 

And remember what a universal cure meant to hospitals and research foundations? Doctors who tried to defend Rife lost their foundations grants and hospital privileges.

 

On the other hand, big money was spent ensuring that doctors who had seen Rife's therapy would forget what they saw. Almost no price was too much to suppress it. Remember that, today, treatment of a single cancer patient averages over $300,000. It's BIG business.

 

Thus, Arthur Kendall, the Director of the Northwestern School of Medicine who worked with Rife on the cancer virus, accepted almost a quarter of a million dollars to suddenly 'retire' in Mexico. That was an exorbitant amount of money in the Depression.

 

Dr. George Dock, another prominent figure who collaborated with Rife, was silenced with an enormous grant, along with the highest honors the American Medical Association could bestow. Between the carrots and the sticks, everyone except Dr. Couche and Dr. Milbank Johnson gave up Rife's work and went back to prescribing drugs.

 

To finish the job, the medical journals, support almost entirely by drug company revenues and controlled by the AMA, refused to publish any paper by anyone on Rife's therapy. Therefore, an entire generation of medical students graduated into practice without ever once hearing of Rife's breakthroughs in medicine.

 

The magnitude of such an insane crime eclipses every mass murder in history. Cancer picks us off quietly...but by 1960 the casualties from this tiny virus exceeded the carnage of all the wars America ever fought. In 1989, it was estimated that 40% of us will experience cancer at some time in our lives.

 

In Rife's lifetime, he had witnessed the progress of civilization from horse-and-buggy travel to jet planes. In that same time, he saw the epidemic of cancer increase from 1 in 24 Americans in 1905 to 1 in 3 in 1971 when Rife died.

 

He also witnessed the phenomenal growth of the American Cancer Society, the Salk Foundation, and many others collecting hundreds of millions of dollars for diseases that were cured long before in his own San Diego laboratories. In one period, 176,500 cancer drugs were submitted for approval. Any that showed 'favorable' results in only one-sixth of one percent of the cases being studied could be licensed. Some of these drugs had a mortality rate of 14-17%. When death came from the drug, not the cancer, the case was recorded as a 'complete' or 'partial remission' because the patient didn't actually die from the cancer. In reality, it was a race to see which would kill the patient first: the drug or the disease.

 

The inevitable conclusion reached by Rife was that his life-long labor and discoveries had not only been ignored but probably would be buried with him. At that point, he ceased to produce much of anything and spent the last third of his life seeking oblivion in alcohol. It dulled the pain and his acute awareness of half a century of wasted effort - ignored - while the unnecessary suffering of millions continued so that a vested few might profit. And profit they did, and profit they do.

 

In 1971, Royal Rife died from a combination of valium and alcohol at the age of 83. Perhaps his continual exposure to his own Rife frequencies helped his body endure abuse for so many years.

 

Fortunately, his death was not the end of his electronic therapy. A few humanitarian doctors and engineers reconstructed his frequency instruments and kept his genius alive. Rife technology became public knowledge again in 1986 with the publication of The Cancer Cure That Worked, by Barry Lynes, and other material about Royal Rife and his monumental work.

 

There is wide variation in the cost, design, and quality of the modern portable Rife frequency research instruments available. Costs vary from about $1200 to $3600 with price being no legitimate indicator of the technical competence in the design of the instrument or performance of the instrument. Some of the most expensive units have serious technical limitations and are essentially a waste of money. At the other extreme, some researchers do get crude results from inexpensive simple, unmodified frequency generators, but this is just as misguided as spending too much money. Without the proper modifications, the basic frequency generator gives only minimal and inconsistent results. Please recall that the actual destruction of the viruses and bacteria, etc. is not accomplished by the frequency displayed on these cheap generators, but by certain shorter harmonics of that particular frequency which are often blocked by the crudity of a cheap and rudimentary instrument itself.

 

This very problem led Rife to ultimately abandon the 'ray tube' design in favor of today's version. The newer technology applies the frequencies and their harmonics to the body through the use of hand-held, footplate, or stick-on electrodes. Proper frequency exposure and flushing of the body with large amounts of clean, pure water is critical to achieve the kind of results Rife got. These procedures are fully explained in the manuals of the best units on the market.

 

So, unless you would be satisfied with sporadic results for minor conditions, it is suggested you use only the highest quality equipment and only the proper, proven procedures in your personal research. If you do, you may discover that nothing can approach what can be achieved through the application of these safe, time-tested frequencies (many for over 65 years)- and all without drugs, surgery, or radiation.

 

One day, the name of Royal Raymond Rife may ascend to its rightful place as the giant of modern medical science. Until that time, his fabulous technology remains available only to the people who have the interest to seek it out. While perfectly legal for veterinarians to use to save the lives of animals, Rife's brilliant frequency therapy remains taboo to orthodox mainstream medicine because of the continuing threat it poses to the international pharmaceutical medical monopoly that controls the lives - and deaths - of the vast majority of the people on this planet.

 

http://www.rense.com

Has the Greatest Health Discovery in History
Been Suppressed?

In the early 1900s, Royal Rife discovered that certain lower life forms could be "devitalized" by subjecting them to certain frequencies produced by an electrical apparatus. He used a combination of AC and DC power to do so. He used a powerful dark field microscope, another device he perfected, which allowed him to watch the effects of his frequency generator on live viruses, bacteria, paramecium, and other potential pathogens. He watched as they were devitalized in a number of ways, either losing their motility, pleomorphing into a different (and hopefully nonpathogenic) form, or actually bursting. Unfortunately, most of his work and the exact design of his frequency generator were lost. This story is detailed in a book called The Cancer Cure that Worked by Barry Lynes.

In a small clinical study during Rife's time, his frequency generator reportedly had a 100% cure rate for the types of cancers that were investigated - sarcomas and carcinomas. He also had a perfect cure rate for other serious diseases of the time, like tuberculosis. The tale of how this work was almost lost to mankind due to fledgling pharmaceutical companies and the American Medical Association is a story for the conspiracy theorists.

Rife's dark field microscope was also an innovation far ahead of its time. It allowed him to view even the tiniest viruses while they were still alive by staining them with light, unlike today's electron microscopes for which the sample must be "fixed" which kills the pathogen being viewed. With this microscope, he saw and reported instances of pleomorphism, which is when an organism mutates, as when a bacterium mutates to a fungal-type lifeform. This was also reported by Bechamps, another early microscopy pioneer, but is still considered anathema to the conventional medical establishment, even though alternative modern researchers working with dark field microscopes have clear proof that it occurs and are willing to show anyone who cares to look.

The exploration of this phenomenon and that of frequency and other electrical effects on pathogens will one day rock the scientific and medical establishments. I will not hold me breathe until this happens, however.

There is little profit, and hence motivation, in developing electrical modalities to treat disease, especially with devices that one can build oneself. It will only come about when so many people know about this treatment, use it, and are more successful using it than with conventional modalities that it is the preferred method to treat disease due to cost, safety, and efficacy. This will come through bit and piece research financed by those how actually need the treatments for themselves and for diseases that conventional medicine has little luck in treating. I have no doubt that this would have never happened had it not been for the internet and its facilitation of instant uncensored worldwide communications.

One factor that may speed progress greatly in this field is the vast amount of commercial applications that exist for this technology which are outside the government-protected field of internal medicine. There is a (rather expensive) "pimple zapper" which uses a single sharp electrode in one hand (and the box in the other) advertised which claims to locally kill bacteria which can cause eruptions. There is a salmonella detector made for egg processing lines which stimulates eggs with the resonant frequency for the bacteria (ala Hulda Clark's syncrometer), but with a laser. If it detects resonance, the egg is kicked out as contaminated. Other potentially very profitable applications are as a safe pesticide in homes (and perhaps farms) and as a disinfectant.

Lately, James Bare has been working to recreate Rife's work, and has a book and video showing how to build a generator which approximates Rife's. His video shows different pathogens succumbing to the effects of his generator, usually bursting or hemorrhaging from the field effects from the transmitter, which is 5 or more feet away.

The Bare device generates a ~27 MHz AC waveform (with a CB) and combines with a DC waveform at varying frequencies. The waveform excites a plasma tube from which the power is transmitted. The high frequency penetrates the body efficiently, but the antipathogenic action is thought to be mostly the harmonics caused by the DC portion.

Bare's Rife device will not generate high enough frequencies to match those discovered by Hulda Clark (in the DC portion) to kill pathogens directly. He must use the harmonics of the frequency generator, and as such he produces a DC waveform which produces enough harmonics to generate them.

This is an inexact science at this time, and due to fluctuations in construction, equipment, tube variations, operating technique, results differ from those building and using the devices, although most admit when they follow Bare's instructions to the letter, they have the best results. Once the device is constructed, cautious experimenters test it on cultures of bacteria, molds, paramecium, etc, to more assure the device produces a useful wave.

The people working with Rife/Bare generators report that it is easy to tell when a frequency generator is causing harmful effects since pain will be felt. They have done experiments on lab rodents and reported that they will not tolerate harmful frequencies without trying to escape. Even so, incautious experimentation with high voltage devices can cause damage or even death, so it is critical that one thoroughly understands the ramifications of dealing with these types of bioelectronics.

The Rife-Bare generator is one of the few types of frequency treatments where the subjects do not come in contact with the device, and some report it works as much as 100 feet away (killing fungus). Other methods that people use to apply frequency to the body include coils, pads, handholds, and other contact applicators. Coils of wire can be stimulated with a frequency and produce a field which will penetrate the body, and some use this method to treat Lyme disease. Pads or handholds can be used to apply voltage directly to the body.

One person reported that he caused possibly permanent nerve and lymph node damage to himself by applying voltage using a wire coil attached to a function generator, amplified to 60 volts, and at tapeworm frequencies as published by Clark. He says he had a tapeworm in a lymph node which "bubbled up" when subjected to the field, killing it but damaging his lymph node.

Human body cells have a resonant frequency at about 1000KHz, and any strong DC modulated signal over 330KHz produces harmonics of significant amplitude in this frequency range. AC signals do not produce these harmonics, so are probably safer to use, but also do not work nearly as well when used in a frequency-inspecific manner.

Hulda Clark uses an AC frequency generator with handholds to kill pathogens in the body. Using a device she developed called a syncrometer, she determined the resonant frequencies of most potential pathogens in the body and proceeded to kill them with an AC frequency generator. This list is published in her book called "The Cure for all Diseases." The only problem with this method is that the pathogen that is causing an illness must be accurately identified before treatment, so that the correct frequency can be used. To run through the entire list of pathogens and dial in the frequencies for all of them for a minimum 3 minutes each requires many hours.

Clark then came up with a zapper. It is a single frequency generator which produces DC square waves at about 30KHz. The lowest frequency given on her list of pathogens is about 80KHz and goes up to 900KHz. Yet, she reports that the DC wave kills many different pathogens in the body. She once speculated that this was from the positive offset DC voltage on the body, but I thought it more likely that the bugs were still dying from frequency effects from the harmonics produced by a zapper's square wave.

A zapper produces an imperfect 30KHz square wave. A square wave is composed of an infinite number of higher frequency AC waves. The AC wave's frequencies and power distribution is analyzed using Fourier transforms. A perfectly symmetrical square wave produces major odd harmonics, that is, AC frequencies at 1,3,5,7,9... times its frequency, and the power available in those harmonics decreases as the multiplication factor increases. A perfect 30KHz zapper produces power at 30, 90, 150, 210, 270 ... Khz. It also produces minor even harmonics.

However, no zapper built to Clark's specs produces a perfect square wave. It produces an unsymmetrical square wave. Most of the ones I have built produce around 16/14 ratio, staying at 8 volts for 16 microseconds, then dropping to 0 volts for 14 microseconds. These values are approximate. There is also usually a spike on the positive-going pulse. These "imperfections" however, add to a zapper's effectiveness. It means that rather than just producing harmonics on the odd multiples, it produces harmonics all over the place. It is impossible to analyze theoretically (for me anyway) and tell just what AC frequencies are being produced.

Add to this another uncertainty factor in that no two zappers are alike when using cheap parts, like from Radio Shack, which have a wide tolerance. I have seen zappers built with the same parts in the same board layout produce different frequencies, one at 28KHz and one at 35KHz, e.g. This leads to a great deal of variability between zappers. For example, the frequency effects of one zapper might be very good at treating salmonella and not touch e. coli, while another one built with the same parts might be highly effective against e. coli and not touch salmonella. There is too much variability. I have one zapper which seems to work best for flu, but will not work against colds, and another that performs best for colds.

Robert Beck is another researcher in the bioelectronic field. His "zapper" is a low frequency bipolar device originally designed to treat HIV. At this writing, it uses a 27V signal at 4Hz, although, like Clark's zapper, frequency is stated not to be important. Beck reports that his device does not kill HIV directly, but merely keeps them from reproducing, which effectively treats them. Even with the high voltage of Beck's zapper, I think it is unlikely that there is enough power at the resonant frequency of HIV to kill it, given the very low frequency. Then again, maybe there is, since viruses are so small, perhaps it only takes a milliwatt or less at the correct frequency to destroy them. And, last I read, Beck's device killed 100% of HIV in 100% of subjects (although this is a far cry from curing AIDS). But perhaps there is something other than frequency effects that devitalize HIV from Beck's machine.

There are also now being built frequency "guns" which produce a non-adjustable set of frequencies and are aimed at a specific part on the body and are modulated by using colored cones on the output. In the few anecdotes I have seen in their use, they appear to be somewhat successful in treating cancerous tumors. One person reported that it did nothing to treat his multiple sclerosis, however, but this is understandable given Clark's assertions on the causes of MS.

I have corresponded with a person who has used frequency generators a great deal in treating illness. He has used homemade ones, commercial function generators, standard and modified zappers. I think he stumbled on to a likely reason the zapper and other frequency devices work.

DNA/RNA are polar molecules and are thus susceptible to frequency effects. Each DNA molecule has a resonant frequency. In general, the simpler the life form the lower the resonant frequency of the being (according to Hulda Clark.) Every cell in a living being has a DNA molecule (half in sperm and ova) and since the DNA for each species are the same size, they have the same frequency. When the cells are subjected to their resonant frequency at sufficient power, they are destroyed.

A zapper with a non-symmetrical waveform provides a limited amount of power in the resonant frequency of each molecule which contains DNA/RNA, which is every living cell. When there are a large amount of the same type of molecule, like in the human body, which is composed of quadrillions, the amount of energy transmitted to each is so small that none are damaged (although they could be due to localized effects of more power being available closest to the electrode site, e.g.). However, this assumes that there is enough power in the frequency of those cells, and Clark states that human body cells have a frequency of above 1MHz. So, if one stays in the lower frequencies and limits power, there is not enough power in the harmonics at 1MHz and above to do damage to a human body.

If there are a small number of some other type of RNA/DNA, as from a minor infection of bacteria, the amount of energy available in that resonant frequency may be enough to destroy the DNA. However, if one has a excess amount of, say, large parasites in the body, the amount of energy is not enough to harm them. The power can be cranked up enough to destroy them, but without knowing the exact frequency at which the pathogens will destruct, it can be risky since the body could be damaged.

There is another effect from a zapper or other pad device that may as important as the frequency effects, however. According to the same guy's speculation, a zapper, or any square wave frequency device, produces hydrogen peroxide in the blood due to its chemistry. Peroxide has antipathogenic effects. But this is only produced in the blood. Still, it would be better to produce it in this manner than ingest it, since consuming more than a few drops can reportedly adversely affect beneficial gut bacteria and not be transmitted to the blood stream intact. He says he can taste the peroxide in his mouth when zapping at high voltages. Perhaps this is the main benefit from using a zapper and any frequency effects are minimal.

After making this post, someone who was involved in the colloidal silver manufacturing business wrote that he suspected that many of the same principles of making colloids also apply to using a zapper. Colloidal silver is made with a zapper-type device and silver wire or plates. He explained that oxygen as formed on one electrode, and hydrogen on the other, as well as the H2O2 and H30, so these could have an effect.

In my experience, zappers are effective for blood borne pathogens but not in the nasal cavities, intestines, or other places inside which there is no blood contained. The same limitation probably applies to all pad or contact devices. Whether it is from the production of chemicals or actual frequency effects, they need the conductive blood to work systemically (although there might still be some local effects that could be put to use.) I think Clark's syncrometer is probably only effective in detecting pathogens with blood exposure as well.

These same limitations apply to variable frequency generator pad devices, but at least (if a bug can be identified) the exact AC frequency can be used without having to rely on harmonics. They can also be used with Rife frequencies for indeterminate pathogens.

Bare-Rife generators are the most effective for treating the entire body and not just the blood, but are most valuable for diseases that are well researched and discussed. Even if a pathogen can be identified as causing a malady, experimentation with a microscope is necessary to determine the correct frequencies to use unless they have been previously determined. The devices lack the ability to use the pathogen frequencies Clark published so harmonics must be used, which makes it an even less exact science because of variations in equipment. Small variations in construction and usage methods can make them ineffectual and they should be well tested and the operators well trained before using them for treatment.

I often recommend zappers for use since I am convinced of their safety. I think that high powered variable frequency tube devices are better at treating illness, but do not recommend their use except by those who research and experiment cautiously because of the possibility of damaging oneself or others. Also, the severity and type of disease should be taken into account. See my article called Zapper Tips for suggestions to get the most out of a zapper.

Addendum: I have now experimented with a Bare Rife plasma tube generator for a number of months. The potential impact that this device will have on the treatment of illness is on par with if not more than all the prescription drugs thus far patented. Combined.

Reproduced from: http://www.medicaltruth.com/rife/elecpath.htm

 

 

 

ROYAL RAYMOND RIFE
& THE CANCER CURE THAT WORKED!

 

Extracted from the book The Cancer Cure That Worked! by Barry Lynes.
 Marcus Books, PO Box 327, Queensville, Ontario, Canada

 

Nexus Magazine, October-November 1993

More than just a cancer cure, Rife's discovery pointed to a new understanding of what we have mistakenly termed 'the germ theory'. Nexus Magazine, October-November 1993 Extracted from the book The Cancer Cure That Worked! by Barry Lynes.  Marcus Books, PO Box 327, Queensville, Ontario, Canada

In the summer of 1934 in California, under the auspices of the University of Southern California, a group of leading American bacteriologists and doctors conducted the first .successful cancer clinic. The results showed that:

a) cancer was caused by a micro-organism;
b) the micro-organism could be painlessly destroyed in terminally ill cancer patients; and
c) the effects of the disease could be reversed.

The technical discovery leading to the cancer cure had been described in Science magazine in 1931. In the decade following the 1934 clinical success, the technology and the subsequent, successful treatment of cancer patients was discussed at medical conferences, disseminated in a medical journal, cautiously but professionally reported in a major newspaper, and technically explained in an annual report published by the Smithsonian Institution.

However, the cancer cure threatened a number of scientists, physicians, and financial interests. A cover-up was initiated. Physicians using the new technology were coerced into abandoning it. The author of the Smithsonian article was followed and then was shot at while driving his car. He never wrote about the subject again. All reports describing the cure were censored by the head of the AMA (American Medical Association) from the major medical journals. Objective scientific evaluation by government laboratories was prevented. And renowned researchers who supported the technology and its new scientif­ic principles in bacteriology were scorned, ridiculed, and called liars to their face. Eventually, a long, dark silence lasting decades fell over the cancer cure. In time, the cure was labelled a 'myth'—it never happened. However, documents now available prove that the cure did exist, was tested successfully in clinical trials, and in fact was used secretly for years afterwards—continuing to cure cancer as well as other diseases.

BACTERIA AND VIRUSES

In 19th century France, two giants of science collided. One of them is now world-renowned—Louis Pasteur. The other, from whom Pasteur stole many of his best ideas, is now essentially forgotten—Pierre Bechamp.

One of the many areas in which Pasteur and Bechamp argued concerned what is today known as pleomorphism—the occurrence of more than one distinct form of an organism in a single life cycle. Bechamp contended that bacteria could change forms. A rod-shaped bacterium could become a spheroid, etc. Pasteur disagreed. In 1914, Madame Victor Henri of the Pasteur Institute confirmed that Bechamp was correct and Pasteur wrong.

But Bechamp went much further in his argument for pleomorphism. He contended that bacteria could 'devolve' into smaller, unseen forms—what he called microzyma. In other words, Bechamp developed—on the basis of a lifetime of research—a theory that micro­organisms could change their essential size as well as their shape, depending on the state of health of the organism in which the micro-organism lived. This directly contradicted what orthodox medical authorities have believed for most of the 20th century. Laboratory research in recent years has provided confirmation for Bechamp's notion.

This seemingly esoteric scientific squabble had ramifications far beyond academic institutions. The denial of pleomorphism was one of the cornerstones of 20th century medical research and cancer treatment An early 20th century acceptance of pleomorphism might have prevented millions of Americans from suffering and dying of cancer.

In a paper presented to the New York Academy of Sciences in 1969, Dr Virginia Livingston and Dr Eleanor Alexander-Jackson declared that a single cancer micro-organ­ism exists. They said that the reason the army of cancer researchers couldn't find it was because it changed form. Livingston and Alexander-Jackson asserted:

"The organism has remained an unclassified mystery, due in part to its remarkable pleomorphism and its stimulation of other micro-organisms. Its various phases may resemble viruses, micrococci, diptheroids, bacilli, and fungi."

THE AMERICAN MEDICAL ASSOCIATION

The American Medical Association was formed in 1846 but it wasn't until 1901 that a reorganisation enabled it to gain power over how medicine was practised throughout America. By becoming a confederation of state medical associations and forcing doctors who wanted to belong to their county medical society to join the state association, the AMA soon increased its membership to include a majority of physicians. Then, by accrediting medical schools, it began determin­ing the standards and practices of doctors. Those who refused to conform lost their licence to practise medicine.

Morris Fishbein was the virtual dictator of the AMA from the mid-1920s until he was ousted on June 6,1949 at the AMA convention in Atlantic City. But even after he was forced from his position of power because of a revolt from several state delegations of doctors, the policies he had set in motion continued on for many years. He died in the early 1970s.

A few years after the successful cancer clinic of 1934, Dr R. T. Hamer, who did not participate in the clinic, began to use the procedure in Southern California. According to Benjamin Cullen, who observed the entire development of the cancer cure from idea to implementation, Fishbein found out and tried to "buy in". When he was turned down, Fishbein unleashed the AMA to destroy the cancer cure. Cullen recalled:

"Dr Hamer ran an average of forty cases a day through his place. He had to hire two operators. He trained them and watched them very closely. The case histories were mounting up very fast. Among them was this old man from Chicago. He had a malignancy all around his face and neck. It was a gory mass. Just terrible, just a red gory mass. It had taken over all around his face. It had taken on one eyelid at the bottom of the eye. It had taken off the bottom of the lower lobe of the ear and had also gone into the cheek area, nose and chin. He was a sight to behold."

"But in six months all that was left was a little black spot on the side of his face and the condition of that was such that it was about to fall off. Now that man was 82 years of age. I never saw anything like it. The delight of having a lovely clean skin again, just like a baby's skin."

"Well he went back to Chicago. Naturally he couldn't keep still and Fishbein heard about it. Fishbein called him in and the old man was kind of reticent about telling him. So Fishbein wined and dined him and finally learned about his cancer treatment by Dr Hamer in the San Diego clinic."

"Well soon a man from Los Angeles came down. He had several meetings with us. Finally he took us out to dinner and broached the subject about buying it. Well we wouldn't do it. The renown was spreading and we weren't even advertising. But of course what did it was the case histories of Dr Hamer. He said that this was the most marvellous development of the age. His case histories were absolutely wonderful"

"Fishbein bribed a partner in the company. With the result we were kicked into court—operating without a license. I was broke after a year."

In 1939, under pressure from the local medical society, Dr R. T. Hamer abandoned the cure. He is not one of the heroes of this story.

Thus, within the few, short years from 1934 to 1939, the cure for cancer was clinically demonstrated and expanded into curing other diseases on a daily basis by other doctors, and then terminated when Morris Fishbein of the AMA was not allowed to "buy in". It was a practice he had developed into a cold art, but never again would such a single mercenary deed doom millions of Americans to premature, ugly deaths. It was the AMA's most shameful hour.

Another major institution which 'staked its claim' in the virgin territory of cancer research in the 1930-1950 period was Memorial Sloan-Kettering Cancer Center in New York. Established in 1884 as the first cancer hospital in America, Memorial Sloan-Kettering from 1940 to the mid-1950s was the centre of drug testing for the largest pharmaceutical companies. Cornelius P. Rhoads, who had spent the 1930s at the Rockefeller Institute, became the director at Memorial Sloan-Kettering in 1939. He remained in that position until his death in 1959. Rhoads was the head of the chemical warfare service from 1943-1945, and afterwards became the nation's premier advocate of chemotherapy.

It was Dr Rhoads who prevented Dr Irene Diller from announcing the discovery of the cancer micro-organism to the New York Academy of Sciences m 1950. It also was Dr Rhoads who arranged for the funds for Dr Caspe's New Jersey laboratory to be cancelled after she announced the same discovery in Rome in 1953. An IRS investigation, instigated by an unidentified, powerful New York cancer authority, added to her misery, and the laboratory was closed.

Thus the major players on the cancer field are the doctors, the private research institutions, the pharmaceutical companies, the American Cancer Society, and also the US government through the National Cancer Institute (organising research) and the Food and Drug Administration (the dreaded FDA which keeps the outsiders on the defensive through raids, legal harassment, and expensive testing procedures).

THE MAN WHO FOUND THE CURE FOR CANCER

In 1913, a man with a love for machines and a scientific curiosity, arrived in San Diego after driving across the country from New York. He had been born in Elkhorn, Nebraska, was 25 years old, and very happily married. He was about to start a new life and open the way to a science of health which will be honoured far into the future. His name was Royal Raymond Rife. Close friends, who loved his gentleness and humility while being awed by his genius, called him Roy.

Royal R. Rife was fascinated by bacteriology, microscopes and electronics. For the next seven years (including a mysterious period in the Navy during World War I in which he travelled to Europe to investigate foreign laboratories for the US government), he thought about and experimented in a variety of fields as well as mastered the mechanical skills necessary to build instruments such as the world had never imagined.

By the late 1920s, the first phase of his work was completed. He had built his first microscope, one that broke the existing principles, and he had constructed instruments which enabled him to electronically destroy specific pathological micro-organisms.

Rife believed that the minuteness of the viruses made it impossible to stain them with the existing acid or aniline dye stains. He'd have to find another way. Somewhere along the way, he made an intuitive leap often associated with the greatest scientific discoveries. He conceived first the idea and then the method of staining the virus with light He began building a microscope which would enable a frequency of light to coordinate with the chemical constituents of the particle or micro-organism under observation.

Rife's second microscope was finished in 1929. In an article which appeared in the Los Angeles Tunes Magazine on December 27, 1931, the existence of the light-staining method was reported to the public:

"Bacilli may thus be studied by their light, exactly as astronomers study moons, suns, and stars by the light which comes from them through telescopes. The bacilli studied are living ones, not corpses killed by stains."

Throughout most of this period. Rife also had been seeking a way to identify and then destroy the micro-organism which caused cancer. His cancer research began in 1922. It would take him until 1932 to isolate the responsible micro-organism which he later named simply the "BX virus".

THE EARLY 1930s

In 1931, the two men who provided the greatest professional support to Royal R. Rife came into his life. Dr Arthur I. Kendall, Director of Medical Research at Northwestern University Medical School in Illinois, and Dr Milbank Johnson, a member of the board of directors at Pasadena Hospital in California and an influential power in Los Angeles medical circles.

Dr Kendall had invented a protein culture medium (called "K Medium" after its inventor) which enabled the 'filterable virus' portions of a bacteria to be isolated and to continue reproducing. This claim directly contradicted the Rockefeller Institute's Dr Thomas Rivers who in 1926 had authoritatively stated that a virus needed a living tissue for reproduction. Rife, Kendall and others were to prove within a year that it was possible to cultivate viruses artificially. Rivers, in his ignorance and obstinacy, was responsible for suppressing one of the greatest advances ever made in medical knowledge.

Kendall arrived in California in mid-November 1931 and Johnson introduced him to Rife. Kendall brought his "K Medium" to Rife and Rife brought his microscope to Kendall.

A typhoid germ was put in the "K Medium", triple-filtered through the finest filter available, and the results examined under Rife's microscope. Tiny, distinct bodies stained in a turquoise-blue light were visible. The virus cultures grew in die "K Medium" and were visible. The viruses could be 'light'-stained and then classified according to their own colours under Rife's unique microscope.

A later report which appeared in the Smithsonian's annual publication gives a hint of the totally original microscopic technology which enabled man to see a deadly virus-size micro-organism in its live state for the first time (the electron microscope of later years kills its specimens):

"Then they were examined under the Rife microscope where the filterable virus form of typhoid bacillus, emitting a blue spectrum colour, caused the plane of polarization to be deviated 4.8 degrees plus. When the opposite angle of refraction was obtained by means of adjusting the polarizing prisms to minus 4.8 degrees and the cultures of viruses were illuminated by the monochromatic beams coordinated with the chemical con­stituents of the typhoid bacillus, small, oval, actively motile, bright turquoise-blue bodies were observed at 5,000X magnification, in high contrast to the colorless and motionless debris of the medium. These tests were repeated 18 times to verify the results."

Following the success, Dr Milbank Johnson quickly arranged a dinner in honour of the two men in order that the discovery could be announced and discussed. More man 30 of the most prominent medical doctors, pathologists, and bacteriologists in Los Angeles attended this historic event on November 20,1931. Among those in attendance were Dr Alvin G. Foord, who 20 years later would indicate he knew little about Rife's discoveries, and Dr George Dock who would serve on the University of Southern California's Special Research Committee overseeing the clinical work until he, too, would 'go over' to the opposition.

On November 22, 1931, the Los Angeles Times reported this important medical gathering and its scientific significance:

"Scientific discoveries of the greatest magnitude, including a discussion of the world's most powerful microscope recently perfected after 14 years' effort by Dr Royal R. Rife of San Diego, were described Friday evening to members of the medical pro­fession, bacteriologists and pathologists at a dinner given by Dr Milbank Johnson in honour of Dr Rife and Dr A. I. Kendall.

"Before the gathering of distinguished men, Dr Kendall told of his researches in cultivating the typhoid bacillus on his new "K Medium". The typhoid bacillus is nonfilterable and is large enough to be seen easily with microscopes in general use. Through the use of "Medium K", Dr Kendall said, the organism is so altered that it cannot be seen with ordinary microscopes and it becomes small enough to be ultra-microscopic or filter­able. It then can be changed back to the microscopic or non-filterable form.

"Through the use of Dr Rife's powerful microscope, said to have a visual power of magnification to 17,000 times, com­pared with 2,000 times of which the ordinary microscope is capable, Dr Kendall said he could see the typhoid bacilli in the filterable or formerly invisible stage. It is probably the first time the minute filterable (virus) organisms ever have been seen.

"The strongest microscope now in use can magnify between 2,000 and 2,500 times. Dr Rife, by an ingenious arrangement of lenses applying an entirely new optical principle and by introducing double quartz prisms and powerful illuminating lights, has devised a microscope with a lowest magnification of 5,000 times and a maximum working magnification of 17,000 times.

"The new microscope, scientists predict, also will prove a development of the first magnitude. Frankly dubious about the perfection of a microscope which appears to transcend the lim­its set by optic science, Dr Johnson's guests expressed them­selves as delighted with the visual demonstration and heartily accorded both Dr Rife and Dr Kendall a foremost place in the world's rank of scientists."

Five days later, the Los Angeles Times published a photo of Rife and Kendall with the microscope. It was the first time a picture of the super microscope had appeared in public. The headline read, "The World's Most Powerful Microscope".

Meanwhile, Rife and Kendall had prepared an article for the December 1931 issue of California and Western Medicine. "Observations on Bacillus Typhosus in its Filtrable State" described what Rife and Kendall had done and seen. The journal was the official publication of the state medical associations of California, Nevada and Utah.

The prestigious Science magazine then carried an article which alerted the scientific community of the entire nation. The December 11, 1931 Science News supplement included a section titled, "Filtrable Bodies Seen With The Rife Microscope". The article described Kendall's filtrable medium culture, the turquoise-blue bodies which were the filtered form of the typhoid bacillus, and Rife's microscope. It included the following description:

"The light used with Dr Rife's microscope is polarized, that is, it is passing through crystals that stop all rays except those vibrating in one particular plane. By means of a double reflecting prism built into the instrument, it is possible to turn this plane of vibration in any desired direction, controlling the illumination of the minute objects in the field very exactly."

On December 27, 1931, the Los Angeles Times reported that Rife had demonstrated the microscope at a meeting of 250 scientists. The article explained:

"This is a new kind of magnifier, and the laws governing microscopes may not apply to it... Or Rife has developed an instrument that may revolutionize laboratory methods and enable bacteriologists like Or Kendall, to identify the germs that produce about 50 diseases whose causes are unknown..."

Soon Kendall was invited to speak before the Association of American Physicians. The presentation occurred May 3 and 4, 1932 at Johns Hopkins University in Baltimore. And there Dr Thomas Rivers and Hans Zinsser stopped the scientific process. Their opposition meant that the development of Rife's discoveries would be slowed. Professional microbiologists would be cautious in even conceding the possibility that Rife and Kendall might have broken new ground. The depression was at its worst. The Rockefeller Institute was not only a source of funding but powerful in the corridors of professional recognition. A great crime resulted because of the uninformed, cruel and unscientific actions of Rivers and Zinsser.

The momentum was slowed at the moment when Rife's discoveries could have 'broken out' and triggered a chain reaction of research, clinical treatment and the beginnings of an entirely new health system. By the end of 1932, Rife could destroy the typhus bacteria, the polio virus, the herpes virus, the cancer virus and other viruses in a culture and in experimental animals. Human treatment was only a step away.

The opposition of Rivers and Zinsser in 1932 had a devastating impact on the history of 20th century medicine. (Zinsser's Bacteriology, in an updated version, is still a standard textbook.) Unfortunately, there were few esteemed bacteriologists who were not frightened or awed by Rivers.

But there were two exceptions to this generally unheroic crowd. Christopher Bird's article, "What Has Become Of The Rife Microscope?", which appeared in the March 1976 New Age Journal, reports:

"In the midst of the venom and acerbity the only colleague to come to Kendall's aid was the grand old man of bacteriology, and first teacher of the subject in the United States, Dr William H. 'Popsy' Welch, who evidently looked upon Kendall's work with some regard."

Welch was the foremost pathologist in America at one time. The medical library at Johns Hopkins University is named after him. He rose and said, "Kendall's observation marks a distinct advance in medicine." It did little good. By then Rivers and Zinsser were the powers in the field.

Kendall's other supporter was Dr Edward C. Rosenow of the Mayo Clinic's Division of Experimental Bacteriology. (The Mayo Clinic was then and is today one of the outstanding research and treatment clinics in the world. The Washington Post of January 6, 1987 wrote, "To many in the medical community, the Mayo Clinic is 'the standard' against which other medical centres are judged.") On July 5-7,1932, just two months after Kendall's public humilia­tion, the Mayo Clinic's Rosenow met with Kendall and Rife at Kendall's Laboratory at Northwestern University Medical School in Chicago.

"The oval, motile, turquoise-blue virus were demonstrated and shown unmistakably," Rosenow declared in the "Proceedings of the Staff Meetings of the Mayo Clinic, July 13,1932, Rochester, Minnesota". The virus for herpes was also seen. On August 26,1932, Science magazine published Rosenow's report, "Observations with the Rife Microscope of Filter Passing Forms of Micro-organisms".

In the article, Rosenow stated:

"There can be no question of the filterable turquoise-blue bodies described by Kendall. They are not visible by the ordinary methods of illumination and magnification... Examination under the Rife microscope of specimens, containing objects visible with the ordinary microscope, leaves no doubt of the accurate visualization of objects or particulate matter by direct observation at the extremely high magnification (calculated to be 8,000 diameters) obtained with this instrument"

Three days after departing from Rife in Chicago, Rosenow wrote to Rife from the Mayo Clinic:

"After seeing what your wonderful microscope will do, and after pondering over the significance of what you revealed with its use during those three strenuous and memorable days spent in Dr Kendall's laboratory, I hope you will take the necessary time to describe how you obtain what physicists consider the impossible.... As I visualise the matter, your ingenious method of illumination with the intense monochromatic beam of light is of even greater importance than the enormously high magnification..."

Rosenow was right. The unique 'colour frequency' staining method was the great breakthrough. Years later, after the arrival of television, an associate of the then deceased Rife would explain, "The viruses were stained with the frequency of light just like colours are tuned in on television sets." It was the best non­technical description ever conceived.

"BX"—THE VIRUS OF CANCER

Rife began using Kendall's "K Medium" in 1931 in his search for the cancer virus. In 1932, he obtained an unulcerated breast mass that was checked for malignancy from the Paradise Valley Sanitarium of National City, California. But the initial cancer cultures failed to produce the virus he was seeking.

Then a fortuitous accident occurred. The May 11., 1938 Evening Tribune of San Diego later described what happened:

"But neither the medium nor the microscope were sufficient alone to reveal the filter-passing organism Rife found in cancers, he recounted. It was an added treatment which he found virtually by chance that finally made this possible, he related. He happened to test a tube of cancer culture within the circle of a tubular ring filled with argon gas activated by an electrical current, which he had been using in experimenting with electronic bombardment of organisms of disease. His cancer culture happened to rest there about 24 hours (with the current on the argon gas-filled tube), and then he noticed (under the microscope) that its appearance seemed to have changed. He studied and tested this phenomenon repeatedly, and thus discovered (cancer virus) filter-passing, red-purple granules in the cultures."

The BX cancer virus was a distinct purplish-red colour. Rife had succeeded in isolating the filterable virus of carcinoma.

Rife's laboratory notes for November 20,1932, contain the first written description of the cancer virus characteristics. Among them are two, unique to his method of classification using the Rife microscope: angle of refraction—12-3/10 degrees; colour by chemical refraction—purple-red.

The size of the cancer virus was indeed small. The length was 1/15 of a micron. The breadth was 1/20 of a micron. No ordinary light microscope, even in the 1980s, would be able to make the cancer virus visible.

Rife and his laboratory assistant E. S. Free proceeded to confirm his discovery. They repeated the method 104 consecutive times with identical results.

In time, Rife was able to prove that the cancer micro-organism had four forms:

1) BX (carcinoma);
2) BY (sarcoma—larger than BX);
3) Monococcoid form in the monocytes of the blood of over 90% of cancer patients.
When properly stained, this form can be readily seen with a standard research microscope;
4) Crytomyces pleomorphia fungi—identical morphologically to that of the orchid and of the mushroom.

Rife wrote in his 1953 book: "Any of these forms can be changed back to "BX" within a period of 36 hours and will produce in the experimental animal a typical tumour with all the pathology of true neoplastic tissue, from which we can again recover the "BX" micro-organism. This complete process has been duplicated over 300 times with identical and positive results.

Rife had proved pleomorphism. He had shown how the cancer virus changes form, depending on its environment. He had confirmed the work of Bechamp, of Kendall, of Rosenow, of Welch, and an army of pleomorphist bacteriologists who would come after him and have to battle the erroneous orthodox laws of Rivers and his legions of followers.

Rife said, "In reality, it is not the bacteria themselves that produce the disease, but the chemical constituents of these micro-organisms enacting upon the unbalanced cell metabolism of the human body that in actuality produce the disease. We also believe if the metabolism of the human body is perfectly balanced or poised, it is susceptible to no disease."

But Rife did not have time to argue theory. He would leave that for others. After isolating the cancer virus, his next step was to destroy it. He did this with his frequency instruments—over and over again. And then he did it with experimental animals, inoculating them, watching the tumours grow, and then killing the virus in their bodies with the same frequency instruments tuned to the same "BX" frequency.

Rife declared in 1953:

"These successful tests were conducted over 400 times with experimental animals before any attempt was made to use this frequency on human cases of carcinoma and sarcoma."

In the summer of 1934,16 terminally ill people with cancer and other diseases were brought to the Scripps 'ranch'. There, as Rife and the doctors worked on human beings for the first time, they learned much. In 1953 when Rife copyrighted his book, he made the real report of what happened in 1934. He wrote:

"With the frequency instrument treatment, no tissue is destroyed, no pain is felt, no noise is audible, and no sensation is noticed. A tube lights up and 3 minutes later the treatment is completed. The virus or bacteria is destroyed and the body then recovers itself naturally from the toxic effect of the virus or bacteria. Several diseases may be treated simultaneously.

"The first clinical work on cancer was completed under the supervision of Milbank Johnson, MD, which was set up under a Special Medial Research Committee of the University of Southern California. 16 cases were treated at the clinic for many types of malignancy. After 3 months, 14 of these so called hopeless cases were signed off as clinically cured by the start of five medical doctors and Dr Alvin G. Foord, MD, pathologist for the group. The treatments consisted of 3 minutes duration using the frequency instrument which was set on the mortal oscillatory rate for "BX" or cancer (at 3-day intervals). It was found that the elapsed time between treatments attains better results than the cases treated daily. This gives the lymphatic system an opportunity to absorb and cast off the toxic condition which is produced by the devitalised dead particles of the "BX" virus. No rise of body temperature was perceptible in any of these cases above normal during or after the frequency instrument treatment. No special diets were used in any of this clinical work, but we sincerely believe that a proper diet compiled for the individual would be of benefit" Date: December 1,1953.

Other members of the clinic were Whalen Morrison, Chief Surgeon of the Santa Fe Railway; George C. Dock, MD, internationally famous; George C Fischer, MD, Children's Hospital in New York; Arthur I. Kendall; Dr Zite, MD, Professor of Pathology at Chicago University, Rufus B. Von Klein Schmidt, President of the University of Southern California.

Dr Couche and Dr Carl Meyer, PhD, head of the Department of Bacteriological Research at the Hooper Foundation in San Francisco, were also present Dr Kopps of the Metabolic Clinic in La Jolla signed all 14 reports and knew of all the tests from his personal observation.

In 1956, Dr James Couche made the following declaration:

"I would like to make this historical record of the amazing scientific wonders regarding the efficacy of the frequencies of the Royal R. Rife Frequency Instrument..

"When I was told about Dr Rife and his frequency instrument at the Ellen Scripps home near the Scripps Institute Annex some twenty-two years ago, I went out to see about it and became very interested in the cases which he had there. And the thing that brought me into it more quickly than anything was a man who had a cancer of the stomach. Rife was associated at that time with Dr Milbank Johnson, MD, who was then president of the Medical Association of Los Angeles, a very wealthy man and a very big man in the medical world—the biggest in Los Angeles and he had hired this annex for this demonstration over a summer of time.

"In that period of time I saw many things and the one that impressed me the most was a man who staggered onto a table, just on the last end of cancer; he was a bag of bones. As he lay on the table, Dr Rife and Dr Johnson said, 'Just feel that man's stomach.' So I put my hand on the cavity where his stomach was underneath and it was just a cavity almost, because he was so thin; his backbone and his belly were just about touching each other.

"I put my hand on his stomach which was just one solid mass, just about what I could cover with my hand, somewhat like the shape of a heart. It was absolutely solid. And I thought to myself, well, nothing can be done for that. However, they gave him a treatment with the Rife frequencies and in the course of time over a period of six weeks to two months, to my astonishment, he completely recovered. He got so well that he asked permission to go to El Centro as he had a farm there and he wanted to see about his stock. Dr Rife said, 'Now you haven't the strength to drive to El Centro.'

"Oh, yes,' said he. 'I have, but I'll have a man to drive me there.' As a matter of fact, the patient drove his own car there and when he got down to El Centro he had a sick cow and he stayed up all night with it. The next day he drove back without any rest whatsoever—so you can imagine how he had recovered.

"I saw other cases that were very interesting. Then I wanted a copy of the frequency instalment. I finally bought one of these frequency instruments and established it in my office.

"I saw some very remarkable things resulting from it in the course of over twenty years."

Footnote:

Biophysicists have now shown that there exists a crucial natural interaction between living matter and photons. This process is measurable at the cellular (bacterium) level. Other research has demonstrated that living systems arc extraordinarily sensitive to extremely low-energy electromagnetic waves. This is to say, each kind of cell or micro-organism has a specific frequency of interaction with the electromagnetic spectrum. By various means, Rife's system allowed adjusting the frequency of light impingeing on the specimen. By some insight he learned that the light frequency could be 'tuned' into the natural frequency of the micro-organism being examined to cause a resonance or feedback loop. In effect, under this condition, it can be said the micro-organism illuminated itself.

Rife extrapolated from his lighting technique, which we may be certain he unde­stood, that specific electromagnetic frequencies would have a negative effect on specific bacterial forms. There can remain no doubt that Rife demonstrated the correctness of his hypothesis to himself and those few who had the courage to look and the perceptual acuity to see! The same new discoveries in biophysics not only explain Rife's principle of illumination; they also explain his process for selective destruction of bacteria. The latter phenomenon is similar to ultrasonic cleaning, differing in delicate selectivity of wave form and frequency. Recently, researchers whose findings have been suppressed, have caused and cured cancer in the same group of mice by subjecting them to certain electromagnetic fields. Rife's work was far more sophisticated. He selected specific microscopic targets, and actually saw the targets explode.

A body of recognised scientific evidence now overwhelmingly supports the original cancer theories articulated and demonstrated by Rife fifty years ago. This includes modern AIDS research.