U.S. patent application number 12/972344 was filed with the patent office on 2012-06-21 for energy charged liquids to enhance enerceutical activation of the alternative cellular energy (ace) pathway in the therapy of diseases.
Invention is credited to William John Martin.
Application Number | 20120152755 12/972344 |
Document ID | / |
Family ID | 46232959 |
Filed Date | 2012-06-21 |
United States Patent
Application |
20120152755 |
Kind Code |
A1 |
Martin; William John |
June 21, 2012 |
Energy Charged Liquids to Enhance Enerceutical Activation of the
Alternative Cellular Energy (ACE) Pathway in the Therapy of
Diseases
Abstract
The alternative cellular energy (ACE) pathway provides a
non-immunological defense mechanism against infectious diseases and
can also function as an effective, non-scarring, tissue repair
mechanism in response to injury. The ACE pathway can be activated
using energy obtained from the ultraviolet light illumination of
neutral red dissolved in alcohol. The effectiveness of the alcohol
used in this procedure is significantly increased by first bubbling
air containing "Water Gas" (otherwise referred to as Brown's Gas or
HHO) through the alcohol. The Water Gas is considered as providing
an additional charge to the alcohol. Water Gas can similarly be
used to charge water and other liquids and to, thereby, increase
the liquid's capacity to interact with various dyes, such as
neutral red, and with other enerceuticals, which are regarded as
being representative of the body's ACE pigments. Various uses are
disclosed for using Water Gas charged alcohol and Water Gas charged
water, for the therapeutic activation of the ACE pathway.
Inventors: |
Martin; William John;
(US) |
Family ID: |
46232959 |
Appl. No.: |
12/972344 |
Filed: |
December 17, 2010 |
Current U.S.
Class: |
205/335 ;
205/464 |
Current CPC
Class: |
A61K 41/0004 20130101;
A61K 33/00 20130101; A61K 45/06 20130101 |
Class at
Publication: |
205/335 ;
205/464 |
International
Class: |
C25B 1/02 20060101
C25B001/02 |
Claims
1. A method for "charging" a liquid comprising the electrolytic
generation of "water gas," (otherwise known as Brown's Gas or HHO),
which is passed through the liquid to be charged, for a sufficient
period of time and in a sufficient quantity, for the liquid to show
a different type and/or intensity of interaction with particles of
added neutral red dye, when this interaction is compared to that
seen when a similar amount of neutral red particles is added to the
same type of liquid which has not been charged; the most noticeable
differences in interaction being i) more rapid dissolving of many
of the particles, with linear streams of dissolved neutral red dye
coming from individual particles; ii) more rapid and more extensive
movements of these particles and of particles which remain
un-dissolved, including the continuing to-and-fro movements of some
individual particles in relationship to more stationary collections
of other particles; the charged liquid plus neutral red dye
solution also having an improved capacity, when compared to the
same liquid in the uncharged form with a similar amount of neutral
red dye, for activating the alternative cellular energy (ACE)
pathway of an individual, as shown by the speed of development
and/or the intensity of direct UV induced fluorescence of the skin
and/or oral cavity, when the charged, compared to the corresponding
uncharged, liquid plus neutral red dye solution, is placed onto the
skin of ACE deficient individuals and the solutions are similarly
illuminated with an ultraviolet (UV) light.
2. The method of claim 1 in which the liquid to be charged is an
alcohol, and in particular, is ethanol.
3. The method of claim 1, in which the liquid to be charged is
water.
4. The method of claim 1, in which the liquids to be charged
include both ethanol and water and which are subsequently used in
combination with each other, with added neutral red dye, followed
by ultraviolet (UV) light illumination, for the purpose of
activating the alternative cellular energy (ACE) pathway of a
subject.
5. The method of claim 1, in which the liquids to be charged
include any of the following: herbal formulations, homeopathic
formulations, terpenes and/or polyphenol containing solutions,
alcoholic beverages; soft drinks; fruit juices; moringa oil; olive
oil; cooking oil; and related products.
6. The method of claim 1, in which the liquids to be charged are
intended to direct application to the skin in the form of
cosmetics, including skin sprays, shampoos and hair products;
footbaths and whole body baths; showers; moistened skin patches;
and related products
7. A means for assessing the effectiveness of a procedure, which is
intended to increase the capacity of a liquid to interact with and
to provide energy to ACE pigments; the method comprising a
determination of whether the procedure is able to modify the type
of interaction seen when small numbers of neutral red particles are
added to the liquid, such that the procedure is deemed to be
effective if there is either i) more rapid dissolving of many of
the particles, with longer and more linear streams of dissolved
neutral red dye coming from individual particles; ii) more rapid
and more extensive movements of these particles and of neutral red
particles which remain un-dissolved, including the to-and-fro
movements of some individual particles in relationship to more
stationary collections of other particles; or iii) more intense
fluorescence upon UV illumination of the neutral red containing
solution.
8. The method of claim 7, in which the procedure consists of the
passage of "Water Gas," obtained by electrolysis of water, into the
liquid.
9. The method of claim 7, in which the procedure comprises any of
the following: physical vortexing; exposing of the liquid to
stationary or rotating magnetic fields; passing water through
minerals, including germanium, tourmaline, zeolites and humic
acids; inclusion of colloidal minerals, including silver, copper
and/or gold; addition of various herbal products, including
terpenes and polyphenols; and even simple sunlight.
Description
CROSS REFERENCE TO RELATED APPLICATIONS
[0001] Co-Pending Patent Application
[0002] Methods for Detection of Ultraviolet Light Reactive
Alternative Cellular Energy Pigments (ACE-pigments) William John
Martin Submitted Dec. 24, 2007. Publication number 20090163831
[0003] Method of assessing and of activating the alternative
cellular energy (ACE) pathway in the Therapy of Diseases. William
John Martin Submitted Submitted Jan. 16, 2008. Publication number
20090181467
[0004] Enerceutical mediated activation of the alternative cellular
energy (ACE) pathway in the therapy of diseases. Submitted May 8,
2008. Publication number 20090280193 Enerceutical activation of the
alternative cellular energy (ACE) pathway in therapy of diseases.
Submitted Feb. 11, 2009. Publication number 20090202442
[0005] Method of using the body's alternative cellular energy
pigments (ACE-pigments) in the therapy of diseases Submitted Feb.
20, 2009. Publication number 20100215763 Urine as a source of
alternative cellular energy pigments (ACE-pigments) in the
assessment and therapy of diseases. Submitted Mar. 5, 2009.
Publication number 20100196297
[0006] Diagnostic value of systemic ACE pathway activation in the
detection by fluorescence of localized pathological lesions.
Submitted Jul. 26, 2010. Publication number 20100291000
[0007] Enerceutical mediated activation of the alternative cellular
energy (ACE) pathway in the therapy of diseases. Submitted July
2010.
[0008] Other Relevant Patents and Patent Applications by William
John Martin:
[0009] Stealth viruses nucleic acids and related methods. U.S. Pat.
No. 5,703,221. Issued Dec. 30, 1997.
[0010] Isolated stealth viruses and related vaccines. U.S. Pat. No.
5,753,488. Issued May 19, 1998.
[0011] Stealth virus detection in the chronic fatigue syndrome.
U.S. Pat. No. 5,985,546. Issued May 26, 1998.
[0012] Stealth virus detection in the chronic fatigue syndrome.
U.S. Pat. No. 5,985,546. Issued Nov. 16, 1999.
[0013] Method of generating hydrogen in gasoline using an
enerceutical product added to magnesium in a hydrogen permeable but
solute impermeable container. Submitted Jul. 18, 2008. Publication
number 20100011657
[0014] Method of generating hydrogen and of selectively
transferring the generated hydrogen to drinking water as a
potential source of alternative cellular energy (ACE). Submitted
Jul. 9, 2008. Publication number 20100008849
[0015] Method of generating hydrogen in drinking water using an
enerceutical product added to magnesium in a hydrogen permeable but
solute impermeable container. Submitted Jul. 14, 2008. Publication
number 20100008850
[0016] Martin W J, Palmer S B. Regenerative wound healing using
copper-silver citrate composition. Submitted Oct. 22, 2008.
Publication number 20100099758 Apr. 22, 2010.
[0017] Patents and Patent Applications Relevant to the Present
Application by Other Inventors: Water Gas (Also called Brown's Gas
and HHO)
[0018] William Rhodes et al Apparatus for the electrolytic
production of hydrogen and oxygen for the safe combustion thereof
Patent number US003262872 Issued Jul. 26, 1966Horvath; Stephen.
Fuel supply apparatus for internal combustion engines. U.S. Pat.
No. 3,980,053. Issued Sep. 14, 1976.
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29, 1977.
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4,081,656. Issued Mar. 28, 1978.
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hydrogen and oxygen for use in a torch or the like. U.S. Pat. No.
4,184,931 Issued Jan. 22, 1980.
[0022] McCambridge, Michael Electrolysis Of Water. U.S. Pat. No.
4,726,888 issued Feb. 23, 1988
[0023] Willey, Alan P. Radford, Neal T. Apparatus for gas
generation. U.S. Pat. No. 5,082,544. Issued Jan. 21, 1992.
[0024] Chiang ,Huang C. Apparatus for generating a mixture of
hydrogen and oxygen for producing a hot flame. U.S. Pat. No.
5,244,558 Issued Sep. 14, 1993. Oshima, Yujiro Hydrogen Generator.
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Hydrogen/Oxygen Fuel Cell. U.S. Pat. No. 5,231,954 Issued Aug. 3,
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Seo, Hirofumi, Hamano;
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cell. U.S. Pat. No. 6,209,493. Issued Apr. 3, 2001.
[0027] Klein; Dennis. Hydrogen generator for uses in a vehicle fuel
system. U.S. Pat. No. 6,866,756. Issued Mar. 15, 2005.
[0028] Holt, Cecil G, Baker, Toby D, Speight, John Leland, Anderson
Iboynne M, Salmon, Jeff, Stevens, David. Water fuel convertor. U.S.
Pat. No. 7,261,062. Issued Aug. 28, 2007. Klein, Dennis J.
Santilli, Ruggero Maria; Apparatus and method for the conversion of
water into a new gaseous and combustible form and the combustible
gas formed thereby. Patent application number 20040149591.
Published Aug. 5, 2004.
[0029] Klein; Dennis. Apparatus and method for the conversion of
water into a clean burning combustible gas for use as an additive
with other forms of fuels. Patent application number 20070151846.
Published Jul. 5, 2007.
[0030] Kang, Song Doug. Use of brown's gas and feeding apparatus of
the brown's gas. Patent application number 20070104797. Published
May 10, 2007.
[0031] Heath; Kevin; Gardner; Barry; Lang; Bill; Lang; Tom. System
and method for improving fuel economy in combustion engines. Patent
application number 20100147232. Published Jun. 17, 2010.
[0032] Kang, Song Doug. Method of treating or alleviating the
symptoms of a lesion in mammal. Patent application number
20100173008 Published Jul. 8, 2010 Dees, James D, Colclesser, Ken.
Hydrogen generator designed for use with gas and diesel engines.
Patent application number 20100282600. Published Nov. 11, 2010.
Haruto. Method for producing electrolyzed water U.S. Pat. No.
5,543,030 Issued Aug. 6, 1996.
[0033] Water Used as Therapy
[0034] Shimamune, Takayuki, Tanaka, Masashi, Nakajima, Yasuo,
Nishiki, Yoshinori, Shimizu, Hideto. Production method of acid
water and alkaline water. U.S. Pat. No. 6,527,940. Issued Mar. 4,
2003.
[0035] Norton, Verdis, Samuelson, Gary L. Method and apparatus for
producing a stabilized antimicrobial non-toxic electrolyzed saline
solution exhibiting potential as a therapeutic. Patent application
number 20090110749. Published Apr. 30, 2009.
[0036] Chen, Ho-Hsien, Huang, Tzou-Chi, Huang, Hao-Hsun, Tung,
Jung-Chang. Method for generating high concentration chlorine
dioxide by means of electrolysis. Patent application number
20080308428. Published Dec. 18, 2008
[0037] Fukai, Toshiharu. Water Having Anticancer Activity and
Method for Making the Same. Patent application number 20100233071.
Publishe Sep. 16, 2010
[0038] Electrolyzer cell for producing acidic or alkaline water.
Patent application number 20100270172. Published Oct. 28, 2010
[0039] Haase, Steven, Haase; Sherry, Holle, Greg, Holle, Tamera.
Ionic foot bath array. Patent application number 20090069870.
Published Mar. 12, 2009.
[0040] References to Published Articles Relevant to the Present
Patent Application Alternative Cellular Energy Pigments
(ACE-pigments): [0041] 1. Martin W J. Alternative cellular energy
pigments mistaken for parasitic skin infestations. Exp. Mol. Path
78: 212-214, 2005. [0042] 2. Martin W J. Alternative cellular
energy pigments from bacteria of stealth virus infected
individuals. Exp. Mol. Path 78: 217-217, 2005. [0043] 3 Martin W J.
Progressive Medicine. Exp Mol Path 78: 218-220, 2005. [0044] 4
Martin W J, Stoneburner J. Symptomatic relief of herpetic skin
lesions utilizing an energy based approach to healing. Exp. Mol.
Path 78: 131-4, 2005. [0045] 5 Martin W J. Etheric Biology. Exp Mol
Path 78: 221-227, 2005. [0046] 6 Martin W J. Stealth Virus Culture
Pigments: A Potential Source of Cellular Energy. Exp. Mol. Pathol.
74: 210-223, 2003. [0047] 7 Martin W J. Complex intracellular
inclusions in the brain of a child with a stealth virus
encephalopathy. Exp. Mol. Pathol. 74: 179-209, 2003. [0048] 8
Martin W J. Photons and phonons: Theoretical aspects of biophysics
and potential therapeutic applications. Proceeding of Neural
Therapy Workshop on Sound and Light Therapy, Seattle, Wash., Feb.
21-23, 2003.
Stealth Adapted Viruses
[0048] [0049] 1 Martin W J Chronic fatigue syndrome among
physicians. A potential result of occupational exposure to stealth
viruses. Explore 2001; 10: 7-10. [0050] 2 Martin W J. Stealth
Viruses. Explore 2001; 10: 17-19. [0051] 3 Durie G M, Collins R.
Martin W J. Positive stealth virus cultures in multiple myeloma. A
possible explanation for neuropsychiatric co-morbidity. Presented
at the Am. Soc. Hematology annual meeting October 2000. [0052]
Martin W J. Chemokine receptor-related genetic sequences in an
African green monkey simian cytomegalovirus-derived stealth virus.
Exp Mol Pathol. 2000; 69:10-6. [0053] 5 Martin W J., Anderson D.
Stealth virus epidemic in the Mohave Valley: severe vacuolating
encephalopathy in a child presenting with a behavioral disorder.
Exp Mol Pathol. 1999; 66:19-30. [0054] 6 Martin W J. Melanoma
growth stimulatory activity (MGSA/GRO-alpha) chemokine genes
incorporated into an African green monkey simian
cytomegalovirus-derived stealth virus. Exp Mol Pathol. 1999;
66:15-8. [0055] 7 Martin W J. Bacteria-related sequences in a
simian cytomegalovirus-derived stealth virus culture. Exp Mol
Pathol. 1999; 66:8-14. [0056] 8 Martin W J. Stealth adaptation of
an African green monkey simian cytomegalovirus. Exp Mol Pathol.
1999; 66:3-7. [0057] 9 Martin W J. Cellular sequences in stealth
viruses. Pathobiology 1998; 66:53-8. [0058] 10 Martin WJ. Detection
of RNA sequences in cultures of a stealth virus isolated from the
cerebrospinal fluid of a health care worker with chronic fatigue
syndrome. Case report. Pathobiology. 1997; 65:57-60. [0059] 11
Martin W J., Anderson D. Stealth virus epidemic in the Mohave
Valley. I. Initial report of virus isolation. Pathobiology. 1997;
65:51-6. [0060] 12 Martin W J. Simian cytomegalovirus-related
stealth virus isolated from the cerebrospinal fluid of a patient
with bipolar psychosis and acute encephalopathy. Pathobiology.
1996; 64:64-6. [0061] 13 Martin WJ. Stealth viral encephalopathy:
report of a fatal case complicated by cerebral vasculitis.
Pathobiology. 1996; 64:59-63. [0062] 14 Martin W J. Genetic
instability and fragmentation of a stealth viral genome.
Pathobiology. 1996; 64:9-17. [0063] 15 Martin W J. Severe stealth
virus encephalopathy following chronic-fatigue-syndrome-like
illness: clinical and histopathological features. Pathobiology.
1996; 64:1-8. [0064] 16 Martin W J. Stealth virus isolated from an
autistic child. J Autism Dev Disord. 1995; 25 :223-4. [0065] 17
Gollard R P, Mayr A., Rice D A, Martin W J. Herpesvirus-related
sequences in salivary gland tumors. J Exp Clin Cancer Res., 1996;
15: 1-4. [0066] 18 Martin W J., Glass R T. Acute encephalopathy
induced in cats with a stealth virus isolated from a patient with
chronic fatigue syndrome. Pathobiology. 1995; 63:115-8. [0067] 19
Martin W J, et al. African green monkey origin of the atypical
cytopathic `stealth virus` isolated from a patient with chronic
fatigue syndrome. Clin Diag Virol 1995: 4: 93-103. [0068] 20 Martin
W J. Stealth viruses as neuropathogens. CAP Today. 1994; 8: 67-70.
[0069] 21 Martin W J. et al. Cytomegalovirus-related sequence in an
atypical cytopathic virus repeatedly isolated from a patient with
chronic fatigue syndrome. Am J Pathol. 1994; 145: 440-51.
[0070] Discovery of Low Density/High Energy Water and High
Density/Low Energy Water
[0071] Wiggins P M. High and low density water in gels. Prog
Polymer Sci. 1995; 20:1121.
[0072] Wiggins P. High and low density water and resting, active
and transformed cells. Cell Biol Internat. 1996; 20:429-435.
[0073] Wiggins P. Life depends upon two kinds of water PLoS 2008;
3:e1406.
[0074] Wiggins P. High and low density intracellular water. Cell
Mol Biol. 2001 Jul;47:735-44.
[0075] Potential Biosynthetic Capacity of Alcohol
[0076] Watson A J, Williams J M. Chemistry. The give and take of
alcohol activation. Science. 2010; 329: 635-6.
STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT
[0077] Not applicable: No Federal funding was received in support
of this patent application.
REFERENCE TO SEQUENCE LISTING, A TABLE OR A COMPUTER PROGRAM
LISTING COMPACT DISK APPENDIX
[0078] Not applicable.
BACKGROUND OF THE INVENTION:
[0079] The invention is based on the following broad conceptual
understanding on how the body can acquire cellular energy other
than through the oxidative metabolism of foods. Essentially, an
alternative cellular energy (ACE) pathway has been identified that
is mediated by the direct energy converting (transducing)
properties of various materials, arbitrarily termed alternative
cellular energy pigments (ACE pigments). Cellular energy generated
by this pathway complements the chemical energy, which is derived
by living organisms from the metabolism of food. The ACE pathway is
postulated to contribute to various physiological functions of the
body. Of particular relevance to this application, the ACE pathway
is involved in non-inflammatory defense and tissue repair
mechanisms. An inadequacy of the ACE pathway can render an
individual susceptible to infection, especially if their immune
system is impaired or if they become infected with microbes, which
cannot evoke a cellular immune response. An inadequate ACE pathway
can also limit the body's capacity to recover from traumatic
injuries; resulting in delayed wound healing with excessive
scarring from over reliance on trauma evoked inflammatory
reactions. The ACE pathway is also anticipated to be involved in
the normal functioning of many organs, including the brain.
Moreover, it is reasonable to presume that many illnesses, not
necessarily of infectious origin, may place an added burden on the
ACE pathway, causing an inadequacy or deprivation of the ACE
pathway with a resulting delaying of the natural healing process.
Conversely, augmenting or correcting an impaired ACE pathway may
facilitate recovery from a wide range of various illnesses.
Moreover, a fully functioning ACE pathway is likely to be a factor
in maintaining wellness, enhancing athletic performance, increasing
cognitive abilities, etc.
[0080] The body's ACE pigments are envisioned as tiny batteries
with differing levels of being "charged." The working model
postulates that uncharged or very poorly charged ACE pigments will
not fluoresce when illuminated directly with an ultraviolet light,
(for example a 13 watt Halco spiral UV light bulb or a Streamlight
365 nm LED stylus penlight.) They will, however, fluoresce when
mixed with certain dyes, including neutral red (e.g. at 0.1 mg/ml;
available from Dudley Chemicals, New Jersey). ACE pigments can also
alter the fluorescence pattern of other dyes, including acridine
orange and Stains-All. Once partially charged, certain ACE pigments
will fluoresce directly when illuminated with UV light. The UV
illumination is able to provide additional energy to the ACE
pigments, such that when more fully charged, the ACE pigments will
no longer fluoresce under UV illumination in either the presence or
absence of neutral red dye. The three energy levels classification
of ACE pigments has proven useful in the clinical assessment of
patients.
[0081] Particles of ACE pigments can be collected from areas of
skin and skin lesions, hair, body fluids, including perspiration,
saliva, urine and blood. In blood, the ACE pigments can be seen
both within cells, including neutrophils and can also be detected
as microscopic particles in serum/plasma samples. A simple home
based fluorescence screening method is for people to collect
saliva, perspiration and/or urine onto a suitable gauze swab,
sponge, wooden spatula, cotton Q-tip and certain filter papers and
to test for UV fluorescence, before and particularly after the
addition of neutral red dye. Direct fluorescence of the body's ACE
pigments can also be tested by directly shining a UV light onto the
skin, or preferably within the mouth. This testing is based on the
indication that partially charged ACE pigments are expected to
directly fluoresce with UV illumination.
[0082] As disclosed in prior patent application, ACE pathway
activation has provided a therapeutic measure for use in patients
with a wide range of illnesses. It is possible, for example, to
utilize ACE pigments in the therapy of herpes simplex virus (HSV)
induced skin lesions. ACE pigments can be collected directly from
the skin lesion or, if present, from bodily fluids, including
perspiration, saliva and even urine. The collected material is
reacted with a solution of freshly prepared neutral red dye, which
is placed onto the HSV skin lesion and illuminated with a UV light.
A healing energy is transferred to the underlying HSV skin lesion,
as shown by the lesion becoming fluorescent when directly
illuminated with the UV light. The fluorescence typically takes 1-2
minutes to begin and persists for several minutes before beginning
to fade. Patients experience symptomatic relief from acute symptoms
and the lesions show marked expedited healing over the ensuring
24-48 hours.
[0083] Major developments in this procedure have included the
following: i) Direct contact of the neutral red dye solution with
the underlying HSV skin lesion is not required. Thus, the collected
ACE pigments with neutral red dye solution can be placed onto a
water impermeable surgical towel or placed within a plastic bag,
(e.g. Zoploc bag), which is then laid onto a water moistened HSV
skin lesion. ii) The procedure can be adapted to treat areas of the
skin on which prior outbreaks of HSV skin lesions have occurred and
future outbreaks might otherwise be expected. Perspiration
collected from these areas of skin will commonly show the presence
of "uncharged" ACE pigments, meaning that they will fluoresce when
mixed with freshly prepared neutral red solution. This material, as
well as other neutral red inducible fluorescing bodily fluids, such
as saliva, can be used to activate direct UV skin fluorescence in
the areas on which HSV recurrences might otherwise occur. By doing
so, the likelihood of any further recurrences, even in emotionally
stressful situations, has been markedly reduced. iii) The need for
collecting ACE pigments from the patients has been eliminated by
the development of various solutions which can directly, or
indirectly, lead to the fluorescing of ACE pigments. Early
solutions included a 10% alcohol (ethanol) solution with trace
quantities of herbal products plus 1% Lidocaine. This formulation
fluoresced brightly with the addition of neutral red and UV
illumination. Moreover, microscopically visible, un-dissolved
neutral red particles displayed persisting and vigorous movements
within the herbal solution. Certain other products, such as a
fluorescing oil from the leaves and seeds of moringa trees, would
directly fluoresce under UV illumination and transfer a fluorescing
capacity to uncharged ACE pigments within virus induced skin
lesions. A terpene-rich tree sap product produced in Japan and
marketed as EH-101 and HB-101, was also effective, especially when
mixed with alcohol. It was next discovered that neutral red dye
would fluoresce with dissolved directly into alcohol, and that this
mixture was as effective as the Lidocaine containing herbal
formulation in activating patient's ACE pigments.
[0084] The focus of therapy was also switched from treating
patients with conventional herpes and papillomavirus infections,
including HSV, herpes zoster virus (HZV) shingles and post-herpetic
neuralgia, and genital warts caused by HPV; and towards the goal of
treating children with autism and adults with mental illnesses.
Prior research had indicated a role for atypical viruses, which are
unable to activate the cellular immune system, in the cause of
autism and other illnesses with a significant impairment of normal
brain functioning. The viruses were grouped under the term "stealth
adapted viruses," and many patients with autism, chronic fatigue
syndrome (CFS) and major psychiatric illnesses are stealth adapted
virus infected, as shown by a virus culture method, which I
developed.
[0085] In a similar sequence of studies as conduced on patients
with HSV infections, I was able to show effective activation of the
ACE pathway using i) perspiration, saliva and even urine derived
ACE pigments from an autistic child to which freshly prepared
neutral red dye was added, and sprayed onto either water
impermeable surgical towels or placed within a Ziploc plastic bag,
placed onto the broad areas of the skin of the child and
illuminated with UV light. ii) The Lidocaine plus herbal
formulation containing 10% alcohol, used as an alternative to
having to collect ACE pigments from the patient, in the
aforementioned procedure. This approach initially provided far more
convenience than parents having to collect ACE pigments from the
child's bodily fluids. A problem arose in the clinical studies,
however, when the Lidocaine plus herbal formulation lost its prior
ACE pathway activating ability. I had no readily available
explanation for the loss of activity.
[0086] The clinical ineffectiveness of the "expired" Lidocaine plus
herbal formulation in systemically activating the ACE pathway in
autistic children was supported by parents' failure to observe the
development of direct fluorescence within the oral cavity of their
child following the procedure. The development of new oral
fluorescence or increased intensity of prior oral fluorescence had
been a reliable indication of ACE pathway activation and correlated
with apparent behavioral improvements. Other parents had associated
clinically successful therapy with the development of discernable
skin fluorescence not only beneath the treated skin area, e.g., the
back or abdomen, but also on the feet, especially the soles. This
observation had led to the choice of placing the Ziploc bags
containing the activating solutions onto water-moistened soles of
the feet of autistic children.
[0087] A temporary switch in treating children with autism was made
from the ineffective Lidocaine plus herbal formulation to using
moringa leaf and seed oil. I soon realized, however, that the
Lidocaine plus herbal solution could be replaced by simply using
absolute alcohol (200 proof ethanol). I further realized that the
absolute alcohol solution with added neutral red could be stored
for several days within a refrigerator and still prove effective in
provoking direct UV fluorescence of the oral cavity. Clinical
progress of a test subject has been quite remarkable over the last
year with marked amelioration of her symptoms of autism. Therapy
sessions have generally been administered at 3-4 week intervals, as
monitored by emotional behaviors (self-awareness, memory of prior
social encounters and empathy, expressed as a sense of humor) and
by the desired minimizing of neutral red dye evoked fluorescence of
the child's saliva. This patent application describes a further
improvement in this basic procedure. To better understand this
advance, it is appropriate to describe some additional background
information, which might at first sight be considered unrelated to
the ACE pathway.
[0088] In what began as an unrelated series of experiments, I have
been producing a copper citrate solution, with and without silver,
as an anti-bacterial product with particular efficacy against Gram
positive bacteria, including methicillin resistant Staphylococcus
aureus (MRSA). A Sears Diehard 12 Volt battery charger provides the
electrical energy for electrolysis. Copper (and silver) anodes and
a copper cathode are placed into a citric acid:potassium carbonate
solution. A surprising and unexpected observation was the
unmistakable, approximately 2-3% increase in the solution volume
occurring during the 1-2 hours electrolysis. The expanded water
volume persisted beyond the electrolysis process. Moreover,
solutions stored for over a month would show a slight reduction in
volume. The increased volume could be restored by 1-2 minutes of
recharging with a 12 Volt battery. In addition to possessing
anti-bacterial activity, the solution was reported by several
patients as providing a very remarkable wound healing benefits.
Although, initially painful when placed on an open wound,
subsequent applications of the solution are well tolerated with far
less pain. The expedited healing was also associated with far less
scarring than would otherwise have occurred.
[0089] The observation of a volume increase in the solution was
reminiscent of studies reported by Dr. Philippa Wiggins of New
Zealand that water can exist as a mixture of low density, highly
energized domains and high density, lower energy domains. She had
suggested that individual water molecules expand by absorbing
chemical energy, for example, derived from the conversion of ATP to
ADP. The expanded water molecules return to the denser, smaller
size as the energy is withdrawn to enable other chemicals to
interact.
[0090] I had been interested in her study because I had previously
noted that there was a fluid volume expansion during the
formulation of Lidocaine plus herbal formulation, plus an apparent
tendency for water to separate from the alcohol solution.
Specifically, I would dissolve the Lidocaine in alcohol and
gradually add water and/or water with diluted tinctures of various
herbal components. By either adding water or allowing much of the
alcohol to evaporate, the Lidocaine would come out of solution as
fine long needles and/or non-structured flocculants. More
interestingly, a clear separation would occur between a water layer
below and an alcohol layer above a band containing the Lidocaine.
Microscopically, the Lidocaine particles would show a flurry of
kinetic movements with the formation of numerous gas bubbles. The
total volume of the solution would also be slightly increased. By
simply adding more alcohol to dissolve the Lidocaine, and then
allowing the alcohol to partially evaporate, the precipitation and
gas formation processes were repeatable over several cycles.
[0091] A possibly related observation is that a tincture of iodine
(containing alcohol) added to an aqueous solution of Lidocaine,
placed into the well of a culture dish, will stimulate a vigorous
flurry of iodine containing droplets. The droplets settle to the
surface of the dish with larger droplets gradually leading to the
dissolving of smaller droplets in close proximity, but not actual
contact with the larger droplets. Again, there is a separation with
the iodine containing droplets being in an aqueous layer, which
becomes separated from an overlaying alcohol layer.
[0092] Again, in a seemingly at first unrelated line of research, I
became interested in augmenting the ignition quality of gasoline. I
could produce hydrogen gas in gasoline by using magnesium metal in
a magnesium chloride solution. I devised a hydrogen gas permeable
membrane container into which I would place the metal and magnesium
chloride. The membrane would allow the generated hydrogen, but not
the magnesium or chloride ions, to mix with the gasoline. As an
offshoot of these studies, I recalled earlier reports that it was
possible to generate a novel form of ignitable water gas using
electrolysis. This gas, which developed midway between the
electrodes, was apparently different from steam and probably also
different from a simple mixture of electrolysis generated hydrogen
and oxygen gas. The basic observation of an ignitable water gas
dates to the 19.sup.th century, but was first patented as a
potential gas for welding by William Rhodes in 1966. Mr. Yull Brown
subsequently reported additional observations on the gas and also
patented some of its potential industrial uses. The gas became more
widely known as Brown's Gas or Brown Gas and offered as a possible
replacement of acetylene in major industrial welding. In his
patents, Mr. Yull Brown hypothesized that electrically separated
"atomic" forms of oxygen and hydrogen were able to yield energy "in
a number of complex chemical reactions." I have found no evidence
for this assumption and have, therefore, opted to use the term
"Water Gas" rather than Brown's Gas in reference to my own studies
on the gas arising, from what I believe is low density, high energy
water molecules.
[0093] Several investigators suggested the potential use of what
they call Brown's Gas, sometimes also referred to as HHO, to
provide additional ignition energy for automobiles. Again, in most
of these reports, the investigators have not clearly distinguished
whether the gas being generated is hydrogen, a mixture of ordinary
hydrogen and oxygen, atomic forms of separated hydrogen and oxygen,
or, as I believe, an atypical form of water vapor. In virtually all
cases, the gas is intended to be added to the air intake into the
combustion chambers of the car and to essentially be an additive to
the combustion energy provided from the ignition of gasoline.
[0094] I had earlier become aware of naturopathic practitioners
wanting to have their patients consume the water condensing from an
ignited "Brown Gas" welding flame. Supposedly, the water had some
health benefits. Moreover, even though it is potentially flammable,
I read an interesting patent by Dr. S. D. Kang on possible health
benefits of spraying "Brown Gas" from a welding machine onto
disease-affected areas of the body. He suggested that the gas was
able to function as if it were water and to, thereby, carrying the
equivalent of moisture into tissues. Dr. Kang also suggested the
possibility of free hydrogen in the gas having potent
anti-oxidizing activity in inhibiting inflammation. From Dr.
Wiggins work, I reasoned that low density, high energy water was
likely to be the source of the therapeutically useful gas.
Arguably, it would have lost some of its energy in the vaporization
process, but might still be able to add sufficient energy to
existing high density, low energy water, leading to the water
becoming more of the low density, high energy form. I further
reasoned that if the electrolytically generated Water Gas could
potentially add energy to regular water, might it not also be able
to add energy to other liquids, and in particular, to alcohol? I
chose this approach, since I knew that alcohol is non-conductive to
electricity and I was reluctant to add electrolytes to alcohol in
an electrolysis reaction, lest the alcohol might ignite.
[0095] Returning to the therapeutic uses of UV illuminated neutral
red dissolved in alcohol and/or in Lidocaine plus herbal
formulation, I, therefore, experimented on the possible additional
benefits, which might be achieved by using a Water Gas activated
alcohol and/or herbal solutions. I re-experimented with the copper
citrate electrolysis and took note of the formation of gas bubbles,
not only on the electrodes, but also from water well away from the
electrodes. These non-electrodes associated bubbles were
presumptively being formed by the vaporization of electrlytically
generated low density, high energy water. I decided to devise ways
of capturing this Water Gas use and to see if it would increase the
reactivity of alcohol with neutral red and further enhance the
therapeutic usefulness of the resulting solution. This patent
application describes the utility of this approach and extends the
basic finding to being able to add energy, subsequently referred to
as charge) to other liquids.
BRIEF SUMMARY OF THE INVENTION
[0096] The passage of electrolytically derived Water Gas into
alcohol greatly enhances the ability of the alcohol to react with
neutral red dye and with the ACE pigments, such that when the
mixtures are illuminated with visible and/or UV light, they can
provide more ACE to an energy deficient individual, when compared
with using untreated alcohol. Water Gas infused (charged) Lidocaine
plus herbal formulations, as well as charged water and other
liquids, are similarly more effective in their interaction with
neutral red dye and with ACE pigments, than are the untreated
(non-charged) control liquids. Methods are described for producing,
monitoring and therapeutically using the charged liquids. Combining
charged alcohol and charged water in various combinations or each
alone, provides a range of solutions for various therapeutic
applications. The applications include procedures, which do not
require the direct contact of the charged solutions with the skin
and/or mucus membranes. The charged solutions can also potentially
be used for direct topical application to the skin and for parental
injections, with or without the inclusion of neutral red dye and/or
ACE pigments. The purpose of the invention is to simplify and to
render more effective some of the existing therapeutic approaches
aimed at enhancing the ACE pathway in humans and animals. The newly
described methods are also applicable to the production of
solutions useful in the assessment of the ACE pathway in an
individual.
BRIEF DESCRIPTION OF THE DRAWINGS
[0097] Not Applicable and none included
DETAILED DESCRIPTION OF THE INVENTION
[0098] Until this invention, UV light illuminated neutral red
dissolved in regular absolute alcohol (200 proof ethanol) has been
the preferred method of choice for activating the ACE pathway in an
individual. Approximately 5 mg of neutral red freshly dissolved in
10 ml of alcohol has generally been placed in a re-sealable plastic
bag (Ziploc) with a small sheet of absorbent paper to help evenly
distribute the fluid. The plastic bag is placed onto a moistened
surface of the body to help minimize intervening air pockets, with
taping as necessary. Preferred sites for placing the bags are the
soles of the feet, palms of the hand and the face. The bag is
usually illuminated with a 13 Watt spiral ultraviolet light bulb
(Halco) positioned closely to the solution. In some experiments two
40 watts, 4 feet long tubular UV bulbs have been used. The
illuminated solution shows a yellow-orange fluorescence in a
darkened room. The therapy session will typically last from 30-60
minutes. Before, during and after the procedure, the treated area
and the oral cavity are examined for using the same type of Halco
UV light, or a more focused UV Streamlight 365 nm LED penlight. In
an ACE deficient individual, one would expect to see the
development of oral fluorescence as an indication of systemic
activation of the ACE pathway. If no inducible fluorescence occurs
within the oral cavity or elsewhere on the body, a tentative
conclusion can be that there is unlikely to be a deficiency of the
ACE pathway, which is correctable using this procedure.
[0099] I produced Water Gas by electrolysis of a 5 liter solution
of citric acid and potassium carbonate (30 grams of each/1 with pH
adjusted to 5.5). A plastic inverted funnel 4'' wide with attached
flexible tubing was held just slightly above the surface of the
solution. The funnel was placed between and away from the two
electrodes, so as to minimize the collection of the hydrogen and
oxygen gases coming directly from the electrodes. The other end of
the flexible tubing from the funnel was attached to a 240 ml
suction canister containing 200 ml alcohol with the inlet tube
being inserted well down below the surface of the alcohol. The
outlet tube from the suction canister was connected to a vacuum
pump. The vacuum driven system was effective in bringing any Water
Gas released from the electrolysis reaction, along with normal air
entering from the sides of the collecting funnel, into the alcohol
solution. Electrolysis and gentle vacuum suctioning proceeded for
at least 4 hours. The Water Gas treated alcohol, from which some
evaporation had occurred, was then compared with untreated alcohol
in various assays.
[0100] The first test was to compare Water Gas treated versus
control alcohol for its reactivity with very small quantities of
neutral red powder. Pumping of the Water Gas through the alcohol
solution clearly altered and enhanced its capacity to dynamically
interact with the neutral red dye. Among the microscopic changes
seen were more rapid dissolving of most of the neutral red
particles, with more sharply defined and strikingly long narrow
streams of dye coming from individual particles. Remaining small
undissolved neutral red particles displayed pronounced and
persisting back and forth movements, which were more marked than
had been previously seen with regular alcohol. Microscopically one
could easily observe individual particles moving towards each other
to form a small clump of particles, but then to abruptly reverse
direction and re-separate, only to again be re-attracted to each
other and reform into a clump. Some particles stayed within the
clumps while others displayed the back and forth movements.
Similar, but less pronounced, movements are also observable when
neutral red is added to untreated alcohol. No such movements are
seen when neutral red is added to plain water.
[0101] The intensity of the attraction of particles into groups,
followed by abrupt repulsion of particles from the groups, as seen
with the treated and apparently "charged" alcohol was reminiscent
of what I had previously observed, but never actually published on,
with ACE pigment particles accumulating in long-term cultures of
stealth adapted viruses. I had also previously noted that the
addition of hydrochloric acid (HCl) would activate movements of the
ACE pigment particles. This experiment was performed because of
reports in the 1930's that intravenous HCl promoted the recovery
from various illnesses. There was also an apparent reduction in
needed oxygen in patients to whom HCl was injected. I inferred this
from the published description of brighter red color of the treated
patients' venous blood
[0102] An important and easily noticeable difference between the
Water Gas treated and untreated alcohol--neutral red solutions is
the more intense fluorescence of the solution containing Water Gas
charged alcohol. It was clear that the Water Gas charged alcohol
was more reactive than untreated alcohol. A determination of volume
expansion could not be made because of evaporation, which occurred
due to the bubbling of the Water Gas through the alcohol.
[0103] The working model is that neutral red dissolved in alcohol
can respond to UV illumination by emitting a form of biological
energy, which can travel beyond the actual neutral red in alcohol
solution. The emitted biological energy can influence the motility
pattern of unicellular microorganisms. This can be observed
microscopically, if a droplet containing motile microorganisms is
placed close to, but physically separated from the alcohol neutral
red solution. For instance, a droplet containing visible, motile
microorganisms is placed on top of a closed transparent Petri-like
dish containing white plus UV light illuminated neutral red:alcohol
solution. In a positive test, the microscopically visible microbes
begin to display erratic, seemingly purposeless movements. While
the effect was clearly seen with neutral red dissolved in regular
alcohol, it was strikingly more apparent in the charged alcohol.
Moreover, it became clear that even regular light from the
microscope was quite effective in generating the distant effect,
which UV illuminated alcohol:neutral red solutions can have on the
motility of microbes. Indications of an effect of white light had
earlier been noted with neutral red in regular alcohol, but were
clearly more readily observed using the charged alcohol.
[0104] A similar series of experiments with confirmatory results
was performed using a small, internet-available, Brown's Gas, or
what I am prefering to call "Water Gas" generator (watertogas.com).
The device, similar to that described in Patent Application
2010/0147232 "System and Method for Improving Fuel Economy in
Combustion Engines," was obtained from Mr. Bill Lang, one of the
authors on the patent application. The basic unit is a 500 ml water
bottle with electrodes extending down from two insulated holes
placed into the lid. Sodium bicarbonate (1 teaspoon or
approximately 3.5 gm) is added to approximately 350 ml of tap water
to render it electrically conductive. Connecting the leads from a
4.5 DC 300 mA transformer to the electrodes produces electrolysis
and gas formation in this "electrolyzer unit." The stem of a "T"
shaped tubing connection piece passes through the lid of the
electrolyzer unit. One side of the "T" is connected to tubing
coming from a small aquarium air pump. The other side of the "T"
connects to tubing, which I extended below the surface of 100 ml
alcohol solution placed in a nearby container. Air passing through
the tubing over the electrolyzer unit is intended to collect the
hydrogen, oxygen and Water Gas coming from the unit and carry it to
the alcohol solution. I generally conducted the early experiments
over 3-4 hours, with a loose lid placed over the alcohol container
to help reduce evaporation of the alcohol. In more recent
experiments, I switched from using sodium bicarbonate in tap water
to 50% seawater, which generated more gas and reduced the time
needed to showing a charging effect on the alcohol to less than 60
minutes.
[0105] I also developed a more standardized assay system for
describing the interaction of neutral red particles placed into a
liquid. Typically, only a few (usually less than 10) fine particles
of neutral red powder, are added to the liquid in a small (1.5 sq
inch) rectangular plastic dish. The particles are viewed
microscopically as they begin to dissolve. A clear determination
can be made of inactive (non-charged) liquids, such as regular
water, in which slowly enlarging rings of defusing neutral red
extend evenly around stationary neutral red particles. Neutral red
particles display a far more dynamic response when placed into a
regular alcohol solution. Narrow, single stream of soluble neutral
red dye will typically emerge from individual particles. The
dissolving particles, as well as small un-dissolved particles, will
also be seen periodically, rapidly moving through the solution and
occasionally interacting by either attraction or repulsion with
other particles. By contrast, in Water Gas charged alcohol, much
longer and narrower streams of dissolving neutral red dye come out
more quickly from the dissolving particles. More impressive, are
the speeds of the movements and the seeming strength of the
attraction and repulsion forces, which especially affect the
particles, which do not fully dissolve in the alcohol solution.
These movements cease when the dish is removed from a light source,
but rapidly resume when the dish is re-illuminated with light.
[0106] A person accustomed to testing his saliva for neutral red
stainable ACE pigment particles reported that energetically moving
microscopic particles were clearly more apparent when he added his
saliva to the charged alcohol, than to regular alcohol. He
confirmed that UV illuminated of a Ziploc bag containing neutral
red dissolved in the charged alcohol, which he placed over the
palms of his hands, was highly effective in systemically activating
his ACE pathway, as evidence by enhancement of the direct UV
fluorescence within his mouth, occurring shortly after beginning a
treatment session. More importantly, he repeatedly used the charged
alcohol: neutral red solution for over a month, without any
apparent loss of its beneficial ACE pathway activation
activity.
[0107] It is not unreasonable to suppose that the charged alcohol
is able to continually absorb energy from the surroundings. Indeed,
some of the absorbed energies would appear to be involved in
possible lipid biosynthesis. This provocative suggestion arose from
observing the formation of numerous small oily bubbles in long-term
(1-2 months) stored charged alcohol:neutral red solutions. Aliquots
from these stored solutions were placed into an open dish and
observed microscopically for dynamically moving, still undissolved
particles. Such particles were readily seen and their movements
were clearly stimulated by both regular white light and UV light.
More fascinating was the extensive formation of minute oily
bubbles, which subsequently coalesced as the alcohol continued to
evaporate. The oily bubbles did not incorporate the neutral red dye
and were easily distinguishable from the neutral red colored
alcohol. Some other materials, which were stained with neutral red,
also precipitated out of the solution in very distinctive banding
patterns. The potential of alcohol to engage in biosynthetic
reactions, including the formation of carbon to carbon bonding, was
recently mentioned in a Science publication.
[0108] The next extrapolation was that the wound healing benefits
observed with the copper citrate solution might have been due, at
least in part, to electrolysis energy activation of the water. I am
well aware of the many claims made regarding ingesting water, which
has been produced by electrolytic treatment of tap water.
Typically, the water is separated on the basis of preferred
ingestion of water with an alkaline pH and/or active electron
donating activity (negative Oxidation-Reduction Potential, ORP).
Other health practitioners have advocated electromagnetic radiation
energies, magnetic energy and sound energies to enhance the health
benefits of water. I was encouraged by Mr. Lang suggestion that
drinking water into which he had passed some Brown's Gas, might
have health benefiting effects and also on Dr. Kang's prior patent
application of blowing what he was calling Brown's Gas onto a site
of injury.
[0109] I, therefore, repeated the above experiments using the newly
installed device to charge water rather than alcohol. Water into
which the aquarium pump was delivering a stream of air, plus
hydrogen, oxygen and Water Gas was periodically sampled and used to
dissolve minute amounts of neutral red powder. The resulting
solutions were also examined for possible UV fluorescence and for
movement patterns of any un-dissolved fine particles of neutral
red. While no fluorescence was seen in any of the resulting neutral
red solutions, there were minor indications for enhanced movements
and dynamic interactions among some of the un-dissolved neutral red
particles.
[0110] The decision was next made to combine the Water Gas treated
alcohol with the Water Gas treated water and to compare these
solutions with those in which only one component had been charged.
In terms of the intensity of fluorescence, and the light stimulated
movements of un-dissolved neutral red particles, more of the
activity seen with 100% charged alcohol was retained using lower
alcohol concentrations diluted in charged water, when compared to
the charged alcohol being diluted in uncharged water. Conversely,
charged water was able to sustain the activity of diluted uncharged
alcohol better than could uncharged water. A striking observation
was the occasional cloudiness, which would immediately develop in
the mixed charged water:charged alcohol solutions, seemingly
because of the formation of very stable emulsion-like alcohol-water
interactions.
[0111] Although not wanting to drink any of the charged
water:charged alcohol-solutions, I did repeatedly and liberally
apply both clear and cloudy solutions on my skin. I had previously
heard from others that the copper citrate solution was helping with
their skin complexion and had begun to see if I could confirm this
effect. I soon realized there was a greater skin appearance
enhancing activity present in the combined charged water: charged
alcohol solutions. A beneficial effect was retained with as low as
5% alcohol.
[0112] Next, I proceeded to show that Lidocaine plus herbal
formulations in 5-10% alcohol solutions could be enhanced in the
intensity of fluorescence and in particle movements when used to
dissolve neutral red if they were prepared with treated alcohol and
treated water than when prepared in the usual manner using
uncharged water and uncharged alcohol. As an alternative approach,
electrolytically generated Water Gas was bubbled through a
regularly prepared Lidocaine plus herbal formulation. This
procedure was effective in enhancing the UV fluorescence and in
stimulating the un-dissolved neutral red particle movement
generating activity of the solutions. Lidociane will react with
tincture of iodine to yield a flurry of rapidly moving
iodine-containing droplets. This activity was enhanced using the
charged Lidocaine plus herbal formulations. As part of these
endeavors, I observed that tincture of iodine would actually form
small droplets when placed directly into the charged alcohol. Thus,
rather than being completely miscible, as it is with regular
alcohol, some of the iodine separated into small droplets.
[0113] Finally, I have used electroylsis system used to bubble
Water Gas through other solutions, some of which I have been
studying for potential therapeutic purposes, including moringa leaf
and seed oil, humic and fulvic acids, a terpene-rich tree sap
solution called EH-101, a mineral-rich solution obtained by
depleting sodium chloride by evaporation of water obtained from the
Great Salt Lake and water to which I have added magnesium chloride.
In each case, I have been able to document changes in reactivity of
the liquid resulting from several hours of exposure to the
electrolysis-generated Water Gas. I next tested a range of
alcoholic beverages, including vodka, gin, whisky, brandy and wine,
to see whether bubbling Water Gas through the liquids would affect
their reactivity with added neutral red particles. While some
indications of a positive effect has been seen, this approach is
somewhat limited by the resulting reduction in the relative amount
of alcohol content because of its greater tendency to evaporate
compared to water.
[0114] In doing these studies, a few (usually less than 20) fine
particles of neutral red powder, are added to the liquid in a small
(1.5 sq inch) rectangular plastic dish. The particles are viewed
microscopically as they begin to dissolve. A clear determination
can be made of inactive (non-charged) liquids, such as regular
water, in which slowly enlarging rings of defusing neutral red
extend around stationary neutral red particles. Neutral red
particles display a far more dynamic response when placed into a
regular alcohol solution. Narrow, single stream of soluble neutral
red dye will typically emerge from individual particles, added to
by the movement of the particles. The dissolving particles, as well
as small un-dissolved particles, will also be seen periodically, be
much more rapidly moving through the solution and occasionally
interacting, by either attraction or repulsion, with other
particles. The long narrow streams of dissolving neutral red and
both the speed of movement and the extent of particle to particle
interaction are much more marked in Water Gas charged liquids, when
compared with the same type of liquid, which has not been charged.
With water, the effect is qualitative since there is essentially no
particle movements in uncharged water, but clearly discernable
activity in charged water. With alcohol, the effect is more
quantitative with far greater activity being seen with charged
versus uncharged alcohol. Combinations of charged water and charged
alcohol are also far more active than using comparable combinations
of uncharged water and uncharged alcohol.
[0115] This research has helped stimulate a new understanding of
the ACE pathway, with many potential improvements on existing
therapeutic efforts to enhance this pathway in the treatment of
illnesses in humans and animals. If I assume that neutral red dye
(and probably many herbal formulations) are comparable to forms of
ACE pigments, then it seems that charging of alcohol and to a
lesser extent the charging of water, facilitate the energy transfer
to ACE pigments. Absorption of sufficient energy by ACE pigments
can render them more responsive to other energy sources, including
but not limited to UV and other wavelengths of light. Activated ACE
pigments can seemingly also create energy fields, which can be
effective in activating other ACE pigments, which can accordingly
change from being uncharged, to partially charged and to more fully
charged. Direct electrolysis of electrical conductive liquids
and/or using Water Gas derived from the electrolysis of electrolyte
containing water, can charge both aqueous and oil solutions and
enhance their interaction with, and energy transfer to, ACE
pigments. Al least for water, charging is associated with an
expansion of its molecules, creating a lower density and,
presumably, higher energy form. Electrical, electromagnetic and
magnetic energies may achieve ACE pathway activation by either
charging water or other liquids, with subsequent transfer of the
energy to ACE pigments, or by the direct charging of the ACE
pigments.
[0116] The solubility patterns of neutral red dye and,
particularly, the movement patterns of the remaining un-dissolved
neutral red particles, have provided a simple method to assess
other potential means of charging water, alcohol and other liquids.
There are many reports that the consumption of water treated in
certain ways can provide significantly greater health benefits than
consuming regular water. The benefits have been variously ascribed
to an alkaline pH, low oxidative reduction potential (ORP, redox,
negative ions), small cluster size or have remained unexplained.
Methods have included physical vortexing; exposing water to
stationary or rotating magnetic fields, passing water through
minerals, including germanium, tourmaline, zeolites and humic
acids; inclusion of colloidal minerals, including silver, copper
and gold; addition of various herbal products, including terpenes
and polyphenols; and even simple sunlight. It is not unreasonable
to suggest that clinical efficacy of various waters may correlate
with the water's ability to interact with, and transfer energy to,
ACE pigments. The neutral red dye linear solubility pattern, along
with the neutral red particles movements and interactions, are
being assessed as provisional surrogate assessment methods to
evaluate various water and other liquid treatment modalities.
[0117] The apparent ability of certain charged liquids, including
water, to directly interact with ACE pigments, can help explain why
even the external application of charged liquids to the skin may
have beneficial effects. Current approaches in this endeavor
include the use of a simple skin spray to soaking part or all of
the body in the treated liquid. Electrolysis units are used in
ionic footbaths, which are commonly displayed at health fairs and
sold on-line for detoxification. Arguably, the units are producing
low density water and water gas, both of which may be entering the
feet, or merely interacting with ACE pigments on the skin of the
feet. Water gas generated from these units could be used in place
of the battery charger and electrolyzer unit, described in the
present patent application.
[0118] The most immediate applications of the research findings
discussed in this patent application, has been the therapeutic use
of UV illuminated neutral red solutions. I have switch from using
regular alcohol to using charged alcohol with apparent clinical
benefit. I can also provide a cost saving by being able to reduce
the need for 100% alcohol with the addition of charged water.
Sealed plastic bags containing the neutral red solutions can be
confidently reused for at least several occasions. Because charging
of the alcohol and of the water appears to allow for white light,
as well as UV light, to further activate ACE pigments, I can now
confidently advocate the use of solutions of charged alcohol
diluted into charged water as a beneficial skin spray, even if not
followed by directly UV light illumination. At a minimum, these
solutions are likely to improve the skin appearance in patients
with skin ACE pigments, which can be further stimulated. Since ACE
pigments can be shown to circulate in blood (as seen in dark field
microscopy), the intravenous injection of osmotically balanced
charged water, with or without charged alcohol, would also be
expected to enhance systemic ACE activity.
[0119] Basically, the newly formulated products will be beneficial
for the localized and/or systemic activation of the ACE pathway in
patients in whom a deficiency of the ACE pathway is contributing to
their illness. Additional information on the ACE pathway and on
illnesses, which may benefit from ACE pathway activation, is
included in the co-pending patent applications, which are included
by reference into this present patent application. The clinical
uses of ACE pathway activation can be extended well beyond the
treatment of stealth adapted and conventional virus infections.
Consideration is being given to activation of the ACE pathway in
patients infected with drug resistant bacteria. It should also
prove useful as a means of achieving wound healing with minimal
scarring from inflammation. Illnesses in which there is an
impairment of oxygen delivery to tissues, from metabolic,
cardiovascular and/or respiratory causes, can also potentially
receive relief from a stimulated ACE pathway. It is, therefore,
important to develop methods of simplifying and enhancing the
efficiency of ACE pathway activation. This goal has been achieved
by the information disclosed in the present patent application.
[0120] The principles, preferred embodiments and modes of operation
of the present invention have been described in the foregoing
specification. The invention, which is intended to be protected
herein, is not to be construed as limited to the particular method
of charging alcohol and other liquids. I clearly understand now
that electrolysis-generated water gas is one of several energy
driven processes that may also be able to similarly charge water
and other liquids. The use of the term alcohol is also not meant to
be restrictive to ethanol, but to also apply to commonly available
other alcohols, including methanol and isopropyl alcohol.
Similarly, although the patent application refers to neutral red
dye, it is known that other dyes, such as acridine orange, can and
have been used to activate the ACE pathway. The patent application
is, therefore, intended to extend to other dyes and enerceutical
products, which can transfer energy to ACE pigments. Additional
advantages and modifications of the basic tenets disclosed in the
present patent application will readily occur to those skilled in
the art and especially upon practicing the currently described
methods. Many variations and changes may be made without departing
from the scope and spirit of the invention as encompassed by the
appended claims.
* * * * *