AIDS can be treated for now, and in the future be cured using the process described here. Most of the current uses of this technology are in another field of science, and the adaptation of use against viruses is a new idea.
Infectious viruses share an elemental life cycle that includes a period in which the virus is a protein shell that encloses DNA molecules, and which has a connector that attaches to human cells through which the virus can inject its DNA into the human cell. The key factor that indicates this treatment is that the efficiency of reproduction in viruses is primarily supported by that virus’s shell (called a virophage). Any strain of virus in a human will have only one size and shape for the shell for its entire population. So it is with HIV, and we can use this to destroy the virus because, of all the properties of the virus, HIV’s shape and size are the most significantly different physical factor from any and all human cells.
Thus far any process that guarantees the physical destruction of the DNA inside HIV will also affect human DNA. Viral DNA is only active when already inside a human cell and we have not found any manner to destroy it once active. The majority of research is trying to prevent closure between the virophage and our cells. This clinical process follows that approach using mechanical force rather than chemicals.
Physics creates a model that defines space in discrete three dimensional boxes and is capable of providing energy to these boxes, which is keyed to the volume of each box. The research would define those boxes to equal the volume of an HIV virophage. It would create an energy field and use the energy to destroy every virophage in the space. This type of physics is called diffraction, and it expresses the interference of conflicting waves.
Ocean waves can be exampled as they are watched from the beach. Surface energy comes toward the beach from many directions at once, and waves collide. As you walk along the beach, you can identify where the energies of all the waves combine to enhance each other; it is a huge, high wave front. Yet nearby, those same waves have not combined as well and cancel each other. This is a jumbled, turbulent, low area. For any wave form of energy, this concept is in place. With higher frequencies such as light, the event of the colliding of waves is referred to as diffraction.
The clinical process would create its own waves in a controlled chamber. These waves would use diffraction theory to distribute the energy into HIV virophage-sized boxes in the chamber, with enough power provided to each box to rupture or otherwise destroy the HIV virophage’s protein casing. As a virophage travels through the field, it assumes the space of one of the boxes and its shell resonates with the energy of the field. That resonance will shatter the shell. Since no human tissue even remotely contains that same volume, they will not resonate. In the human tissues, the energy is distributed, dissipated in a manner not possible for the virophage, which must absorb all the energy. As the energy passes through the blood it contacts all the human components, yet they aren’t the same size as the HIV virophage so the energy doesn’t “stick” to the red cells, the white cells, nor anything but HIV. When the energy does contact HIV, it shreds it at a molecular level.
Think about holograms. They are images created by interference patterns, and much research has been directed toward understanding their use of diffraction . A hologram’s image quality and resolution are a directly related to high-frequency, better-defined illumination sources, usually lasers. Holograms most viewed by the public are recorded in a thin layer of polymer, yet there are types of holograms that utilize a far thicker medium. Imagine a hologram that has as its subject, the HIV virophage. What I propose is very closely related to that concept.
Instead of generating a likeness of a virophage, we will project the interference pattern directly into a thick layer of blood as it passes through a machine. The interference is to create a phenomenon called ‘cavitation’ in a spatial volume level meant to match the HIV virophage. The cavitation contains enough energy to destroy each virus.
A well-known demonstration that this works is a commercial for audio tape. The televised version shows the First Lady of Music singing into a microphone. As the commercial progresses, the woman sings a single note for long duration. The amplified sound, which is emitted by an acoustic speaker, shatters a crystal goblet. Vibration causes the crystals to resonate within the goblet that tears it apart.
That vibration was created by an acoustic speaker whose active element is made mostly of paper. The glass is in most ways much stronger, but at selected frequencies it is far weaker. More importantly, the sound originated in human vocal cords and throat with no damage to either to break the glass, yet glass may readily cut flesh. So it is with the HIV. By selecting the proper frequencies to combine in the proper manner, the waves will pass through all else with little effect, yet they will be permitted to combine and crescendo along the surface of the HIV, tearing it apart.
Sunlight is jumble of frequencies that travel through space together. As these frequencies collide and mesh, they perform work on any material present at the event. This is how our eyes detect light, how sunlight’s infrared rays heat material. It is well known that simple sunlight destroys more viruses than any other factor in our lives. Sunlight is the natural enemy of viruses, and this clinical technology makes this effect more available to the HIV in blood.
There are many ways you can understand this technology in its more practical, every-day forms. Ask a medical ultrasound technician to explain how his instruments are capable of traveling through inches of skin and muscle, and in the midst of kidney nephron cells (some of your body’s most delicate and sensitive tissues) find and destroy hardened kidney stones. Ultrasonic jewelry cleaners use the principles to dissolve grime without affecting the metal or gems.
Theoretical understanding of diffraction theory has been around a very long time, yet the technology required to operate this in a clinical setting has only come to light in the past few years. The mechanics of creating a field of independent waves capable of this activity are challenging. Blood is full of human components that would scatter the waves and reduce the effectiveness. The need for funding to develop the clinical application will be significant.
This treatment is not limited to HIV. By identifying the volume of any virus, field and frequency adjustment can target any virus. Ebola, herpes, leukemia-forming viruses, the list begins here. My opinion is that in the course of killing the HIV in a sample, many or all the other adult viruses present may be destroyed.
Please notice I have used the word “TREATMENT” rather than cure. This process only destroys adult viruses, not affecting those in other phases of life cycle. What I propose is a clinical program that begins reducing the population of adult viruses in the client through a means similar to how we use kidney machines today. A client comes to a center, is hooked up to a machine that extracts his blood, cleanses it of HIV adult virophages, and returns it to him. After a cycle time shown to be effective, the machine is disconnected and prepared for the next client. Since the process is not chemical, concurrent treatment programs will not be affected. This clinical procedure becomes an additional tool to work beside pharmaceutical treatment without affecting them.
By actively reducing the quantity of HIV virophages in the client’s bloodstream, we reduce the effects of the virus. This would give the natural immune system a longer, greater chance to develop its own antiviral program and helps maintain the population of T-cells.
To do all this requires no large new breakthroughs in physical science. Diode laser technology need only be adapted to supply the waveforms and spatial relationships required. Most of us already use diode lasers (there is one in every compact disk player), and the versions required to do this work are only better defined and packaged.
US government heavily subsidized a corporation that put HIV under an electron microscope, so we already have a very detailed geometrical survey of the surface. Actual models of the virus are well defined, with the orientation of the molecules known.
A cure using this technology would require the field to be large enough to envelop an entire animal. Since the life cycle of the virus is known, by administering the treatment repeatedly more often than the virus can reproduce, adult viruses never develop. After a twenty-four hour regimen in which the subject’s entire body is immersed in the treatment at specific intervals, any virus can be eliminated. By the most ambitious estimates a human cure is still years away, even for a baby.
It is possible for our technology to create a functional device within a period of less than four months, and a world-wide clinical network of these machines can be started within the year.
I do not have the HIV virus, and I do not know of anybody in my social world who has the disease. My obligation to my society is to present the technology that permits the society to choose how the technology is used.
I want you to be involved. Copy this letter and send it to a legislator. Contact a physicist and persuade the physicist to help. Convince your local AIDS support group to promote this course. First, read the companion article to this one called, The Clinical Application of A Treatment for AIDS , which is more technical, and describes how the clinical process can work world-wide. It also explains why the technology will be instituted in the future if only for commercial use. It justifies the funding for treatment to even those who cannot accept other forms of treatment for victims of HIV.