Introduction and Discussion
The living process involves survival through regulating growth, adapting
to environmental changes, and activating healing and regenerative
capacities in response to injuries or other disorders occurring within
living entities [1]. The flexibility of the living processes to
optimally adapt to changed circumstances is referred to as allostasis
[2-4]. Failures of allostasis are reflected in persisting and even
worsening diseases, leading to symptoms, shortened lifespan, and even
death.
Living cells require three levels of energy. The first and minimal level
is needed for basic survival. The second energy level is required for
cells to perform the specialized functions, which characterize the
different types of differentiated cells. The third energy level is
needed to respond to injury or other adverse internal or external
influences. These can include injury, infections, toxins, and genetic
alterations. Diseases can be viewed as an insufficiency of cellular
energy (ICE) at one or more of the three levels [5-6]. ICE can be
localized to individual cell types or occur in a more generalized manner
throughout the body.
It had been assumed that the only source of cellular energy for humans
and animals is the calories obtained from the metabolism of consumed
food [7-8]. Yet, calculations of the amounts of work performed by
humans, including maintaining the body’s heat exceed the caloric intake
from food [8]. Moreover, there had to be a different source of
energy for the evolutionary development of the complex chemicals
required in both photosynthesis in plants and oxidative phosphorylation
in all forms of life [9].
Studies on viruses, for which there is no evoked cellular immune
response, [7, 10-12] led to the identification of the alternative
cellular energy (ACE) pathway [7, 13-18]. Virus-damaged cells
growing in tissue cultures can undergo a repair process coinciding with
the development of self-assembling pigmented materials, which can take
the form of particles, threads, and fibers. Replacement of the tissue
culture media with fresh media leads to the rapid reactivation of the
virus cytopathic effect (CPE) [13]. Adding some of the media from
repaired cultures to the fresh media prevents reactivation. Even more
impressive, adding a few of the particles from a repaired culture to the
fresh refeeding media also prevents CPE reactivation [13]. A similar
suppression occurs when using various therapeutic water-based products
that are being marketed as homeopathy. A product called HANSI , an
abbreviation for Homeopathic Activator of the Natural System Immune, and
a closely related product called Enercel , are manufactured by
mixing tinctures of herbal and other compounds in water with 5%
ethanol, with four subsequent 10-fold dilutions. Lidocaine is included
primarily to prevent pain upon intramuscular or intravenous injection.
Apart from the lidocaine there are no detectable materials upon gas
chromatography-mass spectroscopy (GC-MS) analysis of the final products
(unpublished data).
A notable feature of stealth adapted virus-infected cells in cultures,
biopsies from infected patients, and virus-inoculated animals is the
marked disruption of mitochondria [14, 19-20]. The particles,
fibers, and threads developing in the supernatant fluids of infected
cultures can also be seen as intracellular and extracellular materials
in infected tissues [19-20]. Mitochondria use oxidative
phosphorylation to convert adenosine diphosphate (ADP) to adenosine
triphosphate (ATP) by utilizing the chemical energy obtained from food
metabolism [21]. ATP is directly involved in many synthetic cellular
reactions and other cellular activities. It is proposed that chemical
reactions comprise the transfer of KELEA between the reacting molecules,
including water molecules [22]. In this way, additional sources of
KELEA can greatly facilitate chemical reactions, especially through its
loosening of the hydrogen bonding between water molecules [23].
The particles and fibers developing in stealth adapted virus cultures
display a range of energy-related properties [7, 13]. They are
electrostatic, fluorescent in response to both ultraviolet (UV) and
visible light, occasionally ferromagnetic, and move in response to
various external stimuli. They can act as electron donors and mediate
the abiotic synthesis of lipids. As noted above, they can increase the
level of KELEA in water and, thereby, enhance the ACE pathway. The
particles and fibers are accordingly termed ACE pigments [13]. They
provide a mechanistic explanation for the therapeutic uses of other
water-activating compounds and devices, referred to as enerceuticals.
Included in the potential therapeutic benefits is the suppression of
illnesses caused by stealth adapted viruses. There are many additional
health, agricultural, and industrial applications of KELEA [24-30].
Indeed, the generic term KELEA activated water provides a useful
substitute for individually named activated water products, such asHANSI and Enercel .
The proposed fundamental role of KELEA is the prevention of fusion and
annihilation of electrostatically attracted opposing electrical charges
[7, 22-23]. It is a radiant energy that presumably exists in
association with both positive and negative electrical charges. KELEA
causes a quantitative loosening of the electrostatic hydrogen bonding
between water molecules [23]. This is reflected in a lower surface
tension of the water and an increased rate of water evaporation. There
is also the lessening of water attachment to other hydrophilic
chemicals, including electrolytes. This can in turn result in a higher
absorption by the activated water of hydrophobic molecules, including
oxygen. KELEA activation of water and other fluids, including alcohols
and liquid fuels, can be achieved by numerous methods including exposure
of the water to external fluctuating electromagnetic fields and/or the
addition of various dipolar compounds [24-27, 31-33]. If
sufficiently activated, water can itself act as a means of attracting
and transmitting KELEA to nearby water in a continuing process.
Certain forms of the fluctuating electrical activity of the brain and
possibly muscles are seemingly able to attract KELEA for transfer to the
body’s cells and fluids [34]. Empirically, this process is
facilitated by emotional calm, deep sleep, and a joyful sense of
optimism. Conversely, the feelings of stress, fear, and agitation, are
counterproductive to the input of KELEA from the outside environment.
KELEA activation has been observed in water samples placed in a room of
individuals practicing laughing yoga [34]. It is possible to
personally experiment with different ways of similarly increasing the
KELEA level of nearby water. Measures can include observing dynamic
movements of added particles, increased rates of evaporation, lowered
surface tension, and others. Microscopically observing capillary blood
flow below the fingernail can also be informative.
The therapeutic goal is to reinvigorate the body’s self-healing and
regenerative capacities. Like other examples of malfunctioning
processes, there are thresholds beyond which the capacity for
self-correcting responses has been exceeded. Enhancing the ACE pathway
with even relatively little additional KELEA can potentially trigger the
clinical healing of illnesses and restoration of balance to life
processes. This is especially so if there is an accompanying sustainable
increase in the capacity of the brain to attract environmental KELEA.
The concept of KELEA as a radiating force is consistent with the
potential of either contributing to or receiving energy from other
individuals, animals, and even plants. It is, indeed, emotionally
uplifting to view all forms of life as being interconnected via KELEA
and that all persons have the potential capacity to contribute to others
and even to Nature. It is important to subject this concept to rigorous
testing so that if validated, efforts to assist others as well as
oneself can be optimized. Studies are also underway to use optimally use
KELEA in improving agriculture, increasing the efficiency of many
industrial systems, including fuel combustion, and restoring the
capacity for allostasis in Nature.
Acknowledgment: The work was supported by MI Hope Inc. a non-profit
public charity based in South Pasadena CA.