A METHOD OF CURING HIV/AIDS WITH PH-TEA AN ALTERNATIVE MEDICINE
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Patents & Trademarks Office
ACT No. 16 of 2016 -
Laws of Zambia
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INVENTOR: Mendez K.G.C. Fernandez
- CAM, BA.ED, LLB
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November 1, 2016.
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ASSIGNEE: Lords-Hill Laboratories Limited
WEBSITE: www.aidscurefound.com
PHONE: +260 955 889136/ +260 977 889136
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MEDICAL SUPERVISOR:
1. Dr. Mukamba
Mukamba –MD
Ministry of Health (Zambia)
CONSULTANTS:
1. Professor
Garth L. Nicholson - President, Chief Scientific Officer and Research
Professor at the Institute for Molecular Medicine in Huntington Beach,
California, USA.
2. Dr. Peter Duesberg - Professor of Molecular
and Cell Biology at the University of California, Berkeley, USA.
ASSOCIATES:
1. Dr. Edgar
Ngoma – Zambia
2. Mr. Joe
Bales – Publisher for Dr. Boyd Ed Graves (deceased)- USA
LEGAL FIRM:
1. Kennedy
Shepande & Company, Lusaka, Zambia.
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Method of curing HIV/AIDS with PH-TE, an
alternative medicine of molecular crystal devices
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Abstract
The diamagnetic semiconducting molecular
crystals of PH-TEA are utilized for
destroying the AIDS virus, destroying AIDS synergistic pathogens and immunity
suppressing moieties (ISM) in humans. A multitude oral ingestion of the devices
is all that is required for efficacy at levels of about 40 PPM of human blood.
The device molecular crystal contains two mono and two trivalent silver ions
capable of "firing" electrons capable of electrocuting the AIDS
virus, pathogens and ISM. When administered into the digestive system, the
device electrons will be triggered by pathogens, a proliferating virus and ISM,
and when fired will simultaneously trigger a redox chelation mechanism
resulting in divalent silver moieties which chelate and bind active sites of
the entities destroying them. The devices are completely non-toxic.
Claims
What is claimed is:
1. A method of treating HIV/AIDS-sufferers
through oral ingestion of PH-TEA molecular crystals into the digestive and
lymphatic systems of the human subject.
2. A method for increasing white blood cell
counts in HIV/AIDS-sufferers through oral ingestion of PH-TEA molecular
crystals into the digestive system of the human subject.
3. Methods of treating HIV/AIDS-sufferers
according to claims 1-2 where the concentration of said molecular crystals is
approximately 40 PPM of the total blood weight of the human subject.
4. Method of treating
serum pH to increase renal excretion of toxic substance including HIV and all
pH dependent microbes
Description
BACKGROUND OF THE
INVENTION
The present invention relates to the
employment of PH-Tea molecular crystals as anti-HIV devices. This
follows the biochemical understandings of both the HIV and PH-Tea whose
molecular crystals act as stabilized oxygen which causes both oxygenation
and alkalinization of the body’s internal terrain (milieu) on ingestion such
that within 30 to 60 minutes PH-Tea crystals are capable of killing all
anaerobic pathogens and or any pH dependent microbes present in the blood
serum. The consistent and multiple ingestion of this PH-Tea will completely
obliterate acquired immune deficiency syndrome (AIDS) in humans with the resulting
increase in pH. Furthermore, the PH-Tea molecular crystal devices are capable
of killing pathogens and purging both the digestive system and bloodstream of
immune suppressing moieties (ISM) whether or not created by the AIDS virus
(HIV); so as to restore the immune system.
The present invention is based on concepts
previously elucidated in studies conducted on viruses by several scientists
some of whom are Nobel Prize winners. Chief among these cited scientists is
Otto Warburg whose hypothesis now known as the Warburg effect which basically
points to the fact that anaerobic viruses cannot live in an oxygen filled
environment won him the Nobel in medicine.
Dr. Otto Heinrich Warburg, one of the
twentieth century's leading cell biologists, hypothesized thatcancer growth is
caused by tumor cells generating energy mainly by
anaerobic breakdown ofglucose (known
as fermentation, or anaerobic respiration). This is in contrast to healthy
cells, which mainly generate energy from oxidative
breakdown of pyruvate. Pyruvate is
an end product ofglycolysis,
and is oxidized within
the mitochondria.
Hence, and according to Warburg, cancer should be interpreted as a mitochondrial dysfunction.
Cancer, above all other diseases, has countless secondary causes. But, even for
cancer, there is only one prime cause.
His famous lecture now
known as Lindau lecture delivered at the meeting of Nobel Laureates on June 30,
1966 at Lindau, Lake Constance, Germany, Warburg stunned his listening
Laureates with his study revelation here summarized in a few words: the prime cause of cancer is the
replacement of the respiration of oxygen in normal body cells by a fermentation
of sugar.
In 1931 he was awarded
the Nobel Prize in Medicine for this important discovery - that cancer cells
are anaerobic (do not breathe oxygen) and cannot survive in the presence of
high levels of oxygen, as found in an alkaline state. His postulates are now
referred to as The Warburg effect.
This Warburg's
hypothesis has re-gained our attention in an effort to fight off HIV due to
behavioral characteristic similarities of almost all viruses and particularly
between HIV and Rous the cancers virus.
For example, both HIV
and cancer viruses are anaerobic whose cells predominantly produce energy by a
high rate of glycolysis followed by lactic acid fermentation in the cytosol,
rather than by a comparatively low rate of glycolysis followed by oxidation of
pyruvate in mitochondria as in most normal cells.
Similarly, and as
observed by Warburg, if the
prime cause of cancer is the replacement of the respiration of oxygen in normal
body cells by a fermentation of sugar it is thus highly probable the same cause
observed in cancer is the cause of HIV. In the forgoing, the same suggested
cure for cancer is the cure for HIV/AIDS.
Further, on account
that HIV like cancer is ph dependent, a fact supported by medical research
reports published in the Journal of Biological Chemistry of 1991 under the
title: Kinectic Studies of Human immunodeficiency Virus type -1
protease and its Active –Site hydrogen Bond mutant A28S, observes that HIV and other retroviral
proteases belong to the aspartic protease family. However, the only striking
difference of HIV and other asparatic members such as eukaryotic aspartic
protease is in some catalytic properties. Chief among these differences is in
the pH dependence of activity by HIV protease.
The research paper
further reports that HIV-1 protease has an optimal pH for activity in the range
pH 4 - 6 while nearly all other eukarytic aspartic protease have optimal
activities in the range pH 2- 4. The research paper further reports of the
dissociation of HIV-1 protease at pH 7.0 .Thus, manipulating this pH further
will inactivate, dissociate or deactivate HIV completely.
The German Zoologist and microbiologist
Professor Gunther Ederlein who in 1925 described the different stages of a
microbe that is normally present in the blood as tiny colloid protein units
which in degenerative diseases such as cancer and HIV, grow into increasingly
higher bacterial forms and finally into fungi, also found that these
pleomorphic structures dissolved in an alkaline milieu. The pH of the blood is
constant at slightly alkaline or pH 7.4. He advised that since we cannot make
the blood more alkaline than it is naturally slightly alkaline, we thus can
however change the pH of both the lymphatic and digestive systems. This will
eliminate both HIV and cancer tumors and also help to clean the blood of any
pollution caused by pleomorphic microorganisms.
UNDERSTANDING THE MEDICINE - PH-TEA
The Human
Immunodeficiency Virus (HIV) is a retrovirus belonging to the lentivirus famly,
which are characterized by a long incubation period (months even years) and
generally classified as pH-dependent viruses simply because they infect host
cells by fusion with cellular membranes at low pH or in the narrow pH of
between 6.3 to 4.0 (slightly acidic). That means, they become highly infectious
in slightly acidic serum.
In other words, their infectivity is rapid in
this narrow range of pH 6.3 and 4.0. However they become rapidly and
irreversibly inactivated by brief treatment at pH 8.0 (alkaline). That simply
means, such microbes cannot survive at a pH slightly above normal.
Besides being pH
dependant, HIV cells share behavioral characteristics with most cancer cells
which include inflammation and causation of degenerative diseases such as
cachexia, a form of progressive anemia and muscle wasting. This could be the
reason cancers are common in most cases of HIV. And besides, these cells
predominantly produce energy by a high rate of glycolysis followed by lactic
acid fermentation in the cytosol rather than by a comparatively low rate of
glycolysis followed by oxidation of pyruvate in mitochondria as in most normal
cells.
The Lactic acid secreted as a byproduct of
glycosis by HIV enzymes during fermentation (glycosis) is the cause of immune
suppression as this acid kills both the white and red cells which in turn cause
both a reduction in oxygen supply around the body and immune suppression. This
reduction in oxygen causes fatigue syndromes.
The dead cells due to lactic acid begin to rot
when not removed from the system. And when these dead cells rot, molds or yeast
begin to form which grows into fungus. It is this fungus which causes
opportunistic infections such as pneumonia, meningitis, Cancers, and all AIDS
Related Complexes. This fungus also causes blood to clot in the veins which
leads to heart failure and or organ failure.
The continuous buildup of this lactic acid
also causes diabetes, arthritis, gouts and all symptoms of acidosis. This acid
build up is worsened by long term medications such as diabetes and antiviral
drugs which inasmuch produce lactic acid into the blood.
Naturally, the body
often kills damaged cells by apoptosis, a mechanism of self-destruction that
involves mitochondria, but this mechanism fails in both HIV and cancer cells
where the mitochondria are shut down due to the building up of lactic acid and
failings of the kidneys.
Thus, the reactivation
of mitochondria through acid removal in both HIV and cancer cells restarts
their apoptosis program. Then also, manipulating the pH above normal through
alkalinization with PH-TEA will definitely impair the survival ability of HIV
in the body.
OBJECTS OF THE INVENTION
1. The main object of the invention is to
provide for a molecular scale device of PH-TEA crystalline molecules capable of
restoring the immunity of AIDS afflicted humans of the two AIDS etiological
subgroups, candidiasis and wasting syndrome.
2. Another object of the invention is to
provide for immunity restoration in said AIDS afflicted humans through a
multiple ingestion of PH-TEA.
3. Another object of this invention is to
destroy ISM in humans manifesting AIDS diseases of said AIDS etiological
subgroups irrespective as to whether the said ISM was HIV induced, since it is
known that humans may manifest AIDS and still be HIV negative, and thus restore
the immune system in said humans.
4. Another object of this invention is to
destroy the AIDS virus when present in the systems of said AIDS afflicted
humans.
5. Another object of this invention is to
correct serum pH and increase the urinary pH in order to increase renal
excretion of toxic substance such as salicylates and lithium including all
anaerobic microbes such as the AIDS and Cancer viruses.
SUMMARY OF THE INVENTION
This invention relates to a molecular scale
device well elucidated by Dr. Marvin Antelman who defined it as not only
capable of destroying the AIDS virus, but of purging the human bloodstream of
pathogens and restoring immunity to AIDS patients of the candidiasis and
wasting syndrome categories. Said molecular device consists of multitude
crystals of PH-TEA.
The crystal lattice of this molecule has a
unique structure since it is a diamagnetic semiconducting crystal containing
two mono and two trivalent silver ions, which in effect are capable of
"firing" electrons under certain conditions which will destroy AIDS
viruses, other pathogens and immune suppressing moieties (ISM), not only
through the electrocution mode, but also by a binding process which occurs simultaneously
with electron firing, namely, binding and chelation of divalent silver, i.e.,
the resulting product of the electron transfer redox that occur when the
monovalent silver ions are oxidized and the trivalent ions are reduced in the
crystal.
The binding/chelation effect occurs at active
sites of the AIDS virus, pathogens and ISM. Because of the extremely minute
size of a single molecule of this crystal, several million of these devices may
be employed in concert to destroy a virus colony to purge a life support system
of ISM and pathogens with the consumption of only parts per trillion of the
crystal devices.
GENERAL PRESCRIPTION
Moderate Metabolic Acidosis:
ADULT DOSE:
PARANTERAL:
50 to 150 mEq PH-Tea diluted to 1Litre of D5W
to be intravenouslt infused at a rate of 1 to 1.5L/hour. Or
ORAL INGESTION:
325 TO 2000mg orally 1 to 4 times a day. One
gram provides 11.9mEq (mmoL) each of PH-Tea.
NOTE: if the increase in urinary pH is
inadequate, increase the amount of PH-Tea in water solution to 100 to 150 mEq/L
may result in further alkalinization of the urine.
GENERAL PEDIATRIC DOSE
0 TO 12 Years:
1 to 10mEq (84 to 840mg/Kg/day orally in
divided doses; dose should be titrated to desired urinary pH.
REFERENCES
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1. "Is The
AIDS Virus A Science Fiction?" by Peter H. Duesberg and Bryan J.
Ellison, Policy Review, Summer 1990, pp. 40-51.
2. The Prime
Cause and Prevention of Cancer with two prefaces on Prevention -Revised
lecture at the meeting of the Nobel Laureates on June 30, 1966 at Lindau,
Lake Constance, Germany, by Otto Warburg.
3. The Metabolism of Tumors by Otto Warburg.
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4. Pleomorphic Microbes by Gunther
Ederlein.
5. Somatid and Somatoscope by Gaston
Naessens.
6. US Patent # 5,676,977 by Marvin
S. Antelman.
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