Acquired Immune Deficiency Syndrome and the H.I.V. Virus are separate problems.The syndrome is a pre existing unhealthy condition at the cellular,bio-molecular,bio-electric level and the Virus takes advantage of that.
In the Fall of 1990, two medical researchers, Dr.William Lyman and Dr. Steven Kaali, working at Albert Einstein College of Medicine in New York City made an important discovery. They found that they could inactivate the HIV virus by applying a low voltage direct current electrical potential with an extremely small current flow to AIDS infected blood in a test tube. Initially, they discovered this in the lab by inserting two platinum electrodes into a glass tube filled with HIV-1 (type 1) infected blood. They applied a direct current to the electrodes and found that a current flow in the range of 50-100 microamperes (uA) produced the most effective results.Practically all of the HIV viral particles were adversely affected while normal blood cells remained unharmed. The viral particles were not directly destroyed by the electric current, but rather the outer protein coating of the virus was affected in such a way as to prevent the virus from producing reverse transcriptase, a necessary enzyme needed by the virus to invade human cells. Reverse transcriptase allows the virus to enter a human T cell line (called CEM-SS) and commandeer the DNA reproduction machinery. After using the host cell to reproduce itself into thousands of new virii, the swollen host cell (now called syncytia or giant cell) will burst and spew the contents into the bloodstream or lymph system. This is how the virus spreads, but lacking reverse transcriptase, the HIV virus can’t invade the host cell and it becomes vulnerable to destruction by the body’s immune system. (The details of this experiment can be read from Kaali’s patent application.)
Getting the Word Out?
A brief announcement of this discovery appeared in The Houston Post (Mar 20, 1991), then in Science News (Mar. 30, 1991 pg. 207) and later in Longevity magazine: (Dec.1992 pg. 14). Following their work in the Fall of 1990, Kaali and Lyman presented their findings at the First International Symposium on Combination Therapies (an AIDS conference) in Washington DC on March 14th, 1991. Kaali outlined two methods for treating an
AIDS patient with this new therapy: One method involved removing a small amount of blood, electrifying it and then returning it to the patient’s body. The second method involved sewing a miniature electrifying power supply along with two tiny electrodes directly into the lumen of an artery.
For long term treatment, the mini electrifying unit needed to be removed and relocated to a new artery site after 30-45 days since scar tissue and calcification forming around the implant unit would lead to artery blockage. Kaali (along with co-inventor Peter Schwolsky) filed for a patent on this implantable electrifying device on Nov 16, 1990 and nine months later was granted patent #5,139,684 on August 18, 1992. It’s interesting to
note two things here:
1. In order to obtain a patent from the United States Patent Office, Kaali and Schwolsky had to prove that the device works as claimed. Lacking solid proof, US patents are simply not granted.
2. Very often it takes years to obtain a patent, yet this patent was granted in only nine months; a further indication to me of the strength of their demonstrated claims
It’s also interesting to note that other than the 3 publications mentioned above and the March ’91 AIDS conference, nothing again appeared in print, radio, or TV about this important discovery as a potential treatment and cure for AIDS from Kaali and company. Most knowledgeable observers feel that Kaali and Lyman’s discovery was intentionally suppressed following the March ’91 AIDS conference presentation. If AIDS research was on the level and not the sham that it actually is, this should have made front page news around the world. (Around 1999, I was contacted by a woman with AIDS who had managed to reach Dr. William Lyman over the phone. She asked him about his experiments with Kaali regarding blood electrification and if she could obtain the treatment through them. Lyman denied any knowledge of any AIDS treatment or cure.He said he never heard of Dr. Kaali and he had no idea what she was talking about concerning blood electrification and then hung up on her. What does that tell about the power of the people behind the suppression of this discovery?)
Enter Dr Bob Beck
A man named Walter Schnitder drew Dr Robert C. Beck‘sattention to the above-mentioned item in Science News. Beck looked up the patent and decided to try and duplicate the therapy, but he wanted to do it non-invasively; that is by applying the electric current from outside the body.Now if you apply a direct current (DC) potential to the skin, you’re going to get an electrolysis effect and that can cause problems, so Beck
designed a circuit that varied the voltage with an alternating current (AC) at a very low frequency and avoided the electrolysis problem. The waveform that Beck chose is not the typical sine wave seen in AC household outlets, but rather is a bi-phasic square wave, meaning that the waveform voltage has a positive half and a negative half, allowing the current to reverse direction each half cycle. Square waves generate a large number of harmonics. Harmonics are frequency multiples of the original frequency. Odd harmonics are mutiples of the original frequency multiplied by 3, 5, 7 etc. and even harmonics are multipes of 2. For example, the odd harmonics of a 4 Hertz (Hz) square wave would be 12 Hz, 20 Hz, 28 Hz, etc. right up into the radio frequency range.
Georges Lakhovsky, Nikola Tesla and many other scientists had discovered that everything in Nature has its own resonant frequency including every bacteria, virus, parasite, and fungus on the planet. Dr. Royal Rife was able to cure terminal, end stage cancers in the 1930’s by applying the specific resonant frequencies of certain unique bacteria that are always associated with all types of cancers. The steady application of the bacteria’s resonant frequency by plasma wave radiation caused the bacteria to internally shatter and eviscerate, thus destroying it (and all the other bacteria within the body that possessed the same resonant frequency) .
While Kaali and Lyman used DC current to deactivate the AIDS virus, Beck found that he could get he same results using the 3.92HZ square wave.Kaali and Lyman found that the amount of the current applied was the critcal factor and if they kept the current within a range of 50-100 microamperes- they were able to disable the HIV virus within a petri dish as mentioned above. Kaali then worked out a design of a small battery with two tiny electrodes that could be sewn directly into an artery in the arm or leg. By maintaining the current flow between the two electrodes within the 50-100 micro ampere range, the HIV particles were gradually disabled within the bloodstream and the AIDS victim would gradually recover his health. The procedure required surgery that costs about $5,000 (at that time). The implanted electrodes would cause scarring of the artery walls,so they had to be removed and implanted in a new section of an artery every month or so, costing another $5,000 each time the procedure was done. It took about 6 or 7 months to see a substantial improvement in the AIDS patient. Beck studied Kaali’s patent and tried applying the electrodes to the skin directly over those arteries that were close enough to the skin surface. The 50-100 micro ampere current could be created within the artery by electromagnetic induction allowing the entire therapy to be applied externally, without the need for implanting electrodes into the arteries. The device he put together to accomplish this is today called a blood
electrifier. Beck started by applying his blood electrifier to himself. He originally placed the electrodes over leg arteries near the ankles of either leg, then changed the location to two different spots on the arm, and finally found that it worked just as well if he placed the two electrodes near each other over the ulnar and radial arteries just behind the wrist. To find the correct location in order to center the electrodes exactly over the arteries, Bob Beck
recommends carefully feeling for the pulse of either artery and marking the path of the artery with a ball point pen. You can then memorize the correct location and align the electrodes over the artery path precisely and hold them in place with a stretchy wrist band.
The video below is by a brilliant autopsy Doctor
who pioneered the use of non standard cell staining techniques and found hidden Pathologies
which,if known would have saved patients lives.
reported by the Silver Institute (a group which keeps silver investors appraised of all of the new uses for silver in business and industry), the EPA has recently approved the use of a product called Axen30, a liquid spray disinfectant similar to colloidal silver, for use in child day-care centers, preschools, schools, gymnasiums and children’s activity centers.
Axen30 is a dilute formula consisting of 30 ppm silver used as a spray disinfectant. But here’s the interesting part:
The EPA-approved advertising claims for Axen30 include a 30-second kill time and a 24-hour residual kill time on standard indicator bacteria, a two-minute kill time on the resistant bacteria MRSE and VRE, a 10-minute kill time on fungi, a 30-second kill time on HIV Type I, and a 10-minute kill time on other viruses.
Now that’s amazing – a proven 30-second kill time against HIV (i.e., Human Immunodeficiency Virus, aka the AIDS virus), and a ten minute kill time against other viruses!
In an experiment at the Albert Einstein College of Medicine in New York in 1990 it was shown that currents between 50 and 100 uA seem to alter the outer protein layer of HIV viruses so that they can no longer attach to receptor sites on white blood cells and they also lost the ability to reproduce. It has been stated that HIV positive users of electro-therapy can expect a negative p24 surface antigen or PCR test after 30 days.The colloidal silver make doubles a Direct Current Applicator 3-28 Volts.one way flow.The blood electrifier doubles as a Direct Current applicator 3-28 volts, Alternating direction 4 times per second, not to be confused with AC current.
By separating the syndrome from the virus it gives us an entrance into the case.
The Syndrome is an unhealthy and weak state of the surface proteins of cells.The normal expected defenses are not there and the cell has large undefended pores through which the virus can enter.The internal mitochondria are polluted and in bad shape, unable to “energize the cell.The reason A.i.d.s. keeps coming back is that the virus hides inside organs and the lymph system andglands. Some “muscle” must be used to “get them” there and this is the Magnetic Pulser and the Blood Electrifier shown below.If the viral load is lowered while simultaneously healing the cells on a Biomolecular level, there is some hope of recovery.Colloidal Silver kills viruses other opportunistic infections which complicate the condition.A cell uses NATURAL Vitamin-C to make spikes which prevent viruses from coming near.
COLLOIDAL SILVER AND VIRUS INHIBITION
“The interaction of nanoparticles with biomolecules and microorganisms is an expanding field of research. Within this field, an area that has been largely unexplored is the interaction of metal nanoparticles with viruses.
In this work, we demonstrate that silver nanoparticles undergo a size-dependent interaction with HIV-1, with nanoparticles exclusively in the range of 1-10 nm attached to the virus.
The regular spatial arrangement of the attached nanoparticles, the center-to-center distance between nanoparticles, and the fact that the exposed sulfur-bearing residues of the glycoprotein knobs would be attractive sites for nanoparticle interaction suggest that silver nanoparticles interact with the HIV-1 virus via preferential binding to the gp120 glycoprotein knobs.
Due to this interaction, silver nanoparticles inhibit the virus from binding to host cells, as demonstrated in vitro.”
Fungus is a dangerous ally with HIV Immno compromised conditions
“Aspergillus sp are among the most common environmental molds, found frequently in decaying vegetation (compost heaps), on insulating materials (in walls or ceilings around steel girders), in air
conditioning or heating vents, in operating pavilions and patient rooms, on hospital implements, or in airborne dust”. Aspergilli are the second most common systemic mycoses and account for nearly
30% of fungal infections found at autopsy. They often appear after antibiotic or antifungal therapy (to which they are usually resistant) ; this is one distressing area of fighting systemic mycoses–sometimes when eliminating one type, another becomes prominent .
“Invasive fungus infections caused by aspergillus spp. occur most frequently in immunocompromised patients. A high infection-associated death rate of up to and over 50% is attributed even today to these fungi. The disease in humans is caused mainly by Aspergillus fumigatus, Aspergillus flavus and Aspergillus niger”
Myalgic Encephalitis, now more commonly called Chronic Fatigue Syndrome or Fibromyalgia.
cause of death is due to systemic fungus infestations or mycoses. Conventional theory assumes that these are secondary to tumours or the AIDS virus, while the observed pleomorphic life cycle shows
that these and their fungal stages are the primary cause why people die of cancer and probably AIDS.The reason for the lethal effects of severe mycoses is probably a combination of poisoning of the
energy-producing mitochondria inside cells by fungal toxins and the destruction of RED BLOOD CELLS by pleomorphics. (SEE THE PLEOMORPHIC PAGE.
These pleomorphics(BACTERIA) not only fill the inside of red blood cells and deplete them of nutrients, they also form spines and long protrusions in the cell wall when they move out into the plasma. Someone with myasthenia gravis, an autoimmune disease, once mentioned that he was shocked to see that most of his red blood cells looked like black sea-urchins. These erythrocytes(RED BLOOD CELLS) can no longer supply nutrients to the body and are quickly destroyed inthe spleen.
This is the real cause of severe anaemia that is so common in advanced cancer and various other diseases. In the end stages of cancer nearly 100% of erythrocytes are strongly infested and dysfunctional. This then leads to cachexia (muscle wasting with extreme fatigue) as the leading cause of death in cancer and AIDS. However, as shown in the longer video, with special Enderlein vaccines even in advanced cancer the erythrocytes could be returned to health within one month with simultaneous shrinking of existing metastases. You may wonder how it is possible for a single cause such as an overgrowth of the blood with pleomorphics(16 different kinds of bacteria) to lead to many different diseases. The answer is basically the same as why a cyclone or hurricane can destroy one building and leave another one undamaged, or rips off the roof of one and causes water damage in another. When the immune system is severely weakened then any pathogens have free range, and the weakest organ will be the first to crumble.
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