FAQs
A bit of biology
Do all pathogens have DNA and RNA?
While all bacteria and higher organisms contain both DNA and RNA, viruses are different. Some viral genomes are made of DNA, while others are made of RNA. Some RNA viruses go through a temporary DNA stage, while other RNA viruses have no DNA at any stage of their cycle.
Do all pathogens have cell walls?
Since viruses are not cells, they are generally surrounded by a lipid envelope or protein capsid layer instead of a cell “wall”.
Bacteria are cells, and generally have one of three types of covering: a gram positive or gram negative wall (both of those types contain a “wall” structure, along with one or two membranes); or thirdly, a simple membrane lacking a “wall” component. The latter is typical of bacteria such as mycoplasmas and L-forms (1).
There have been instances noted wherein some walled bacteria partially or totally lose their wall, and transform to a membranous type of bacteria. (1)
Do frequencies “blow up” the pathogen DNA?
It is unknown the precise mechanism how frequencies may influence pathogen DNA or RNA. There may be several, or possibly sequential mechanisms involved in the process. One compelling theory is that the electromagnetic emissions may easily influence the large number of charged free ions and polar water molecules that surround the densely negative-charged DNA molecule.(2) The disruption of the pathogen DNA’s surrounding layer, may make it difficult for the DNA to function in an optimal way.
Will frequencies affect the DNA in my cells, the same way it affects the DNA of the pathogen?
This is a question of major interest and importance. It cannot be answered easily, because the many models of frequency delivery systems emit their frequencies in different ways, using various types of electromagnetic fields, waveforms and power levels. However, there is considerable science available that could help us understand some cellular effects.
There are many differences between bacterial (prokaryotic) and mammalian (eukaryotic) cells (3), some or all of which may help to explain effects from frequency delivery systems:
1. Their DNA structure is very different. Mammalian DNA is bonded to proteins called histones, which wrap and fold the DNA into a manageable size. Bacterial and viral DNA do not contain histones. The histones may provide electrical shielding to mammalian DNA, as compared to bacterial and viral DNA.
2. DNA in eukaryotic cells is surrounded by a nucleus and nuclear membrane. Bacterial cells do not contain a nucleus.
3. Eukaryotic cells are generally 10-30 times larger in linear dimension, and 1,000-10,000 times greater in volume than typical bacterial cells. This results in a much smaller surface to volume ratio in eukaryotic cells as compared to bacterial.
4. Because of the difference in wall and membrane components, bacterial cells carry a much denser negative electrical charge on their outside surface than eukaryotic cells do. Also, the cell walls of bacteria are highly porous, and the pores are relatively large. These traits allow easy movement of charged ions and proteins through the pores. While these characteristics are necessary for bacterial metabolic processes to take place, it’s possible they can be used to advantage when influencing the bacteria with electromagnetic frequency delivery systems.
5. The constituents of bacterial membranes are chemically and electrically different than those of eukaryotic membranes.
6. Bacteria possess no internal cytoskeleton, as do eukaryotic cells. This would include microtubules and actin filaments. Furthermore, bacteria do not perform endocytosis or exocytosis.
Individually or collectively, all these factors and possibly others may play a part in why certain pathogenic organisms are influenced more easily than eukaryotic animal and plant cells by frequency delivery systems. Recent years have seen many projects being carried out by major researchers at highly regarded laboratories and universities, all of which are too numerous to review in this small space.
References
1. Mattman, Lida H. Cell wall deficient forms, 3rd ed. Boca Raton: CRC Press, 2001.
2. Takashima, Shiro. Electrical Properties of Biopolymers and Membranes. Bristol: Adam Hilger, 1989.
3. Alberts, Bruce, et al. Molecular Biology of the Cell,, 3rd ed., pp. 22-25, 481-485, 521-523, 554-555. New York: Garland Publishing, 1994.