Blue Flower

THE CURE FOR HIV/AIDS

A METHOD OF CURING HIV/AIDS WITH PH-TEA AN ALTERNATIVE MEDICINE

 

 

Patents & Trademarks Office

ACT No. 16 of 2016 - Laws of Zambia

INVENTOR: Mendez K.G.C. Fernandez

- CAM, BA.ED, LLB

November 1, 2016.

ASSIGNEE: Lords-Hill Laboratories Limited

WEBSITE: www.aidscurefound.com

PHONE: +260 955 889136/ +260 977 889136

_______________________________________

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.

 

 


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 that cancer growth is caused by tumor cells generating energy mainly by anaerobic breakdown of glucose (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 of glycolysis, 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


 

 

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.

 

4. Pleomorphic Microbes by Gunther Ederlein.

 

5. Somatid and Somatoscope by Gaston Naessens.

 

6. US Patent # 5,676,977 by Marvin S. Antelman.