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.