27 February 2008

Freuencies: Sound can create life and heal life

Sound, the Trigger for Life by John Stuart Reid

Viktor Schauberger, the brilliant Austrian scientist, working in the 1940’s and 50’s, may have been the first to study micro vortexes in water. Interestingly, micro vortexes carry the same basic structure as DNA! More recently, scientists in Hong Kong have demonstrated that micro vortexes can be created in the laboratory and are used to manipulate single DNA molecules. In other words, the bore of the micro vortex approaches that of the DNA double helix. It seems like divine irony that the very mechanism that may have created DNA is now being employed to manipulate it!

To summarise, we propose that the first strands of DNA were created in the micro vortex environments of primordial hydrothermal vents. Should micro vortexes be discovered within microscopic bubbles we have a model that begins to resemble living cells: a membrane (the surface of the bubble) with strands of DNA within.

If sound was indeed the trigger for life, it follows that sound alone should be able to heal life. The sound of ocean waves is certainly calming but the sounds imbedded within them may healing at a level we can currently only guess at.

24 February 2008

Mycoplasma - Why the Lyme Flu Goes On and On

Many chronic dieseases today are caused or aggravated by bioengineered mycoplasma that now infect most of the population. The recent Lyme flu has caused long term sinus and other problems in some of those afflicted. The root of this problem appears to be mycoplasma.

Don Scott's work on investigating the origin of these mycoplasma is provided below. Those wanting more detailed analysis of the origins of Lyme disease should read Lab 257, a thoroughly researched analysis of decades of violation of EPA regulations and common sense at Plum Island. Click here for an excellent video of blood microscopy showing the Lyme mycoplasma. They are the small spherical white dots in the video that tend to attach to red blood cells and cause energy depletion. Dr. Shyh-Ching Lo mentioned by Don Scott below has a patent on Mycoplasma fermentans extracted from AIDs patients. These are seen in the photo above and in the video.

Most research on Lyme disease focuses on eliminating the Borrellia spirochetes with antibiotics as these are the most immediately disabling. However, the spirochetes can be removed in a few hours with frequencies. The more difficult organisms are the viruses, the fungi, and the mycoplasma. The mycoplasma are often infected with nanobacteria so eliminating them will cause a nanobacteria herxheimer reaction. Thus nanobacteria needs to be dealt with as well as the primary symptom of nanobacteria infection is the need for excessive amounts of sleep. This is commonly seen in those with chronic Lyme infections.

Recent research has focused on systematically disassembling micoplasma with frequencies that target various parts of the organism and disperse the DNA. There are quite a few mycoplasma strains in the Lyme complex and it is a nontrivial task to untangle them all. Subscribers will automatically receive these frequencies.

Mycoplasma the Linking Pathogen in Neurosystemic Diseases

by Donald W. Scott, MA, MSc
Pathogenic Mycoplasma
A Common Disease Agent Weaponized

Several strains of mycoplasma have been "engineered" to become more dangerous. They are now being blamed for AIDS, cancer, CFS, MS, CJD and other neurosystemic diseases.

There are 200 species of Mycoplasma. Most are innocuous and do no harm; only four or five are pathogenic. Mycoplasma fermentans (incognitus strain) probably comes from the nucleus of the Brucella bacterium. This disease agent is not a bacterium and not a virus; it is a mutated form of the Brucella bacterium, combined with a visna virus, from which the mycoplasma is extracted.

The pathogenic Mycoplasma used to be very innocuous, but biological warfare research conducted between 1942 and the present time has resulted in the creation of more deadly and infectious forms of Mycoplasma.

Researchers extracted this mycoplasma from the Brucella bacterium and actually reduced the disease to a crystalline form. They "weaponized" it and tested it on an unsuspecting public in North America.

Dr Maurice Hilleman, chief virologist for the pharmaceutical company Merck Sharp & Dohme, stated that this disease agent is now carried by everybody in North America and possibly most people throughout the world.

Despite reporting flaws, there has clearly been an increased incidence of all the neuro/systemic degenerative diseases since World War II and especially since the 1970s with the arrival of previously unheard-of diseases like chronic fatigue syndrome and AIDS.

According to DR Shyh-Ching Lo, senior researcher at The Armed Forces Institute of Pathology and one of America's top mycoplasma researchers, this disease agent causes many illnesses including AIDS, cancer, chronic fatigue syndrome, Crohn's colitis, Type I diabetes, multiple sclerosis, Parkinson's disease, Wegener's disease and collagen-vascular diseases such as rheumatoid arthritis and Alzheimer's.

DR Charles Engel, who is with the US National Institutes of Health, Bethesda, Maryland, stated the following at an NIH meeting on February 7, 2000: "I am now of the view that the probable cause of chronic fatigue syndrome and fibromyalgia is the mycoplasma..."

I have all the official documents to prove that mycoplasma is the disease agent in chronic fatigue syndrome/fibromyalgia as well as in AIDS, multiple sclerosis and many other illnesses.

Of these, 80% are US or Canadian official government documents, and 20% are articles from peer-reviewed journals such as the Journal of the American Medical Association, New England Journal of Medicine and the Canadian Medical Association Journal. The journal articles and government documents complement each other.

See Dr. Mercola's web site for the remainder of this article.

23 February 2008

LYME CONTROVERSY: Better find a Lyme literate physician!

Vaccine Companies Investigated for Manslaughter

If you have a newborn, before you let anyone give your baby a Hepatitis B vaccine, read Dr. Mercola's recommendationa.

Vaccine Companies Investigated for Manslaughter

A formal investigation has been launched by French authorities against two managers from drug companies GlaxoSmithKline and Sanofi Pasteur. A second investigation for manslaughter has also been opened against Sanofi Pasteur MSD.

The investigations are in response to allegations that the companies failed to fully disclose side effects from an anti-hepatitis B drug used between 1994 and 1998.

During this time, close to two-thirds of the French population, and almost all newborn babies, received a hepatitis B vaccine. The vaccination campaign was halted after concerns rose over the shot’s side effects.

Thirty plaintiffs, including the families of five people who died after the vaccination, have launched a civil action in the case against the drug companies.

22 February 2008

ABPA - Frequency Foundation Standard Configuration

The Frequency Foundation has spent a decade of research on fine tuning ABPA hardware for frequency transmission. We assisted in the development of special cabling and green antennae boards that are factory approved. Many different hardware addons have been tested and the Harmony Evolution chip has proven the most useful in improving effectiveness.

The configuration of the ABPA system is extremely important to get maximum benefit. While any frequency generator such as the FSCAN can be connected to the ABPA, the F165 frequency generator has been the most useful because of its programmability along with the quality of its signal and its output of mulitple channels. This device is recommended for anyone who wants to get the most utility out of the ABPA. It is mandatory for those wanting to use Lyme frequencies as the sets are so complex it is not feasible to manually program them on another device.

It is also essential to set up the hardware exactly as indicated here. Failure to do this will seriously degrade the output of the ABPA. For those able to test the ABPA signal who find an improved configuration, the Frequency Foundation will test that configuration at no charge and confirm your findings. Otherwise use the standard configuration shown here.

In 2007, ABPA's were upgraded with a new chip. This means:

- More ABPA internal memory
- More comprehensive internal ABPA software

Dale Fawcett handles hardware sales for Frequency Foundation. Give him a call at +1 360 598-6585 or send him email at dale.fawcett@gmail.com for questions on hardware.

A frequency generator can be attached to an Advanced BioPhoton Analyzer (ABPA) and the device will transmit an ultralow frequency carrier wave with the generated frequencies superimposed and filtered by a target photo. The person in the photo acts as a tuner that receives the frequencies.

F165/F70 frequency generators are used for this purpose as they put out multiple channels of high quality signals that are programmable by a scripting language. The Frequency Foundation has upgraded some of the F165 generators (shown in the photo above) to F170 devices that simultaneously emit 7 channels of frequencies. This allows you to target precisely and simultaneously all or most of the frequencies for a parasite, for example, which typically has 4-8 frequencies. This full scale assault on the life form radically shortens treatment time. Similarly for bacteria that form communities which have multiple frequencies for different stages of the community life cycle.

The recommended hardware setup has evolved over the years to make it more than 1000 times as effective when I first discovered the capability of the ABPA to transmit frequencies. It is critical that the hardware be set up exactly right to get the desired effects. Only with precisely the right hardware configuration and precisely the right frequencies can you get consistently good results.

From left to right in the photo above, we see that following switches/connectors on the F165 frequency generator:

1. The black knob turns up the voltage of the signal to a maximum of 16 volts for the output port directly to the right of the knob.
2. The output port to the right of the knob needs to be connected to the factory approved cable with a blue box in the center. When the other end of the cable is plugged into the ABPA, a red LED lights up on the ABPA side of the blue box. The knob is turned up so that the red LED on the F165 side of the blue box exactly matches the brightness of the LED on the ABPA side. This matches the impedance of the frequency generator signal to the ABPA and provides maximum effectiveness. The factory cable improved output by a factor of 5 over previous strategies of placing an ABPA wire connected to the F160 under the ABPA input well.
3. The second output jack to the right of the black knob is a 5 volt output suitable for driving Rife plasma devices.
4. The next jack to the right is for a USB cable to connect to a computer. A computer is used to program the F165 and can drive the device directly or download a program into the F165 so that it can run stand alone.
5. Next we have a power jack.
6. To the right of the power jack is an on/off switch.

A second factory approved option for the ABPA that has been developed by the inventor for use in frequency applications is a green antenna board (see photo above). It improves the effectiveness of ABPA frequency transmission by a factor of 10. (Call Dale Fawcett for ABPA accessories, F-Scan or Transfer Factor info at 360 598-6585). The effects of the cable and the antennae are multiplicative. You get 50 times the effectiveness of a frequency transmission compared to a system without them.

The Advanced Biophoton Analyzer (ABPA)is a device that can be used for many purposes. One of them is to broadcast frequencies on a very low frequency carrier wave that can penetrate the earth and is independent of distance. The frequency effect on a living organism at a remote location is comparable to being in the room with an EMEM plasma device or directly connected to electrodes from a contact device like an FSCAN when all recommendations on hardware setup are followed.

The recommended setup of the ABPA is show in the photo above:

1. The switches are set from left to right - off, off, off, auto, auto, on, send, auto.
2. The first jack on the front right of the ABPA is for power.
3. The second jack is a mini female phono jack for input. The recommended setup is a MONO mini male dual phono jack that connects both the antennae and the factory approved cable with the blue box to the ABPA. Do not use a stereo dual phono jack as the ABPA will receive no signal and the ABPA will not transmit frequencies.
4. A Polaroid photo of the target should be put on the antenna. For high power transmission, it is recommended that a high resolution digital photo be put in the photo well. This combination will increase the effectiveness of the transmission by another factor of 5 or more. This gives us 5x10x5 times the effectiveness of earlier implementations.
5. Finally, a Harmony Evolution Chip should be put on the antennae. This improves the output of the ABPA by another factor of 25 so we have a system that is 5x10x5x25 or thousands of times better than the first implementation of these systems.
6. There are proprietary hardware strategies that the Frequency Foundation uses to enhance output even further, making remote transmission as effective as local application of frequencies in most cases.

The ABPA has some advantages over direct contact with frequency devices as it is able to monitor the energy system of the target and only transmit information that will balance that energy system and bring it into a higher energy state. It is a self-correcting device that works with and enhances the effect of frequency generators attached to it. This only occurs if a Polaroid photo of the target is in the circuit. It can be in the photo well, on the antenna, or in the input or output wells. All of these are on the same circuit.

The only challenge remaining is finding the right frequencies for your purposes. As Dr. Royal Rife once said, if you have the wrong frequency or set of frequencies you will get no effect. For help in finding the right frequencies for your needs, contact the Frequency Foundation.

13 February 2008

Viral Frequencies: not new but nice to see scientists waking up!

A three-dimensional model of an HIV virus. Researchers are exploring the use of lasers and sound waves to attack viruses. Credit: 3DScience.com

New Way to Kill Viruses: Shake Them to Death
By Michael Schirber, Special to LiveScience
posted: 05 February 2008 09:27 am ET

Scientists may one day be able to destroy viruses in the same way that opera singers presumably shatter wine glasses. New research mathematically determined the frequencies at which simple viruses could be shaken to death.

"The capsid of a virus is something like the shell of a turtle," said physicist Otto Sankey of Arizona State University. "If the shell can be compromised [by mechanical vibrations], the virus can be inactivated."

Recent experimental evidence has shown that laser pulses tuned to the right frequency can kill certain viruses. However, locating these so-called resonant frequencies is a bit of trial and error.

"Experiments must just try a wide variety of conditions and hope that conditions are found that can lead to success," Sankey told LiveScience.

To expedite this search, Sankey and his student Eric Dykeman have developed a way to calculate the vibrational motion of every atom in a virus shell. From this, they can determine the lowest resonant frequencies.

As an example of their technique, the team modeled the satellite tobacco necrosis virus and found this small virus resonates strongly around 60 Gigahertz (where one Gigahertz is a billion cycles per second), as reported in the Jan. 14 issue of Physical Review Letters.