2.4 billion (2,400,000,000) B.C.
Project Earth ... A Report (part of the Health-4-All Package)
Viruses begin to be present on the Earth at this stage of Earth's history. Composed of complex combinations of chemicals and minerals which have combined to form large molecules of matter, they are neither considered alive nor dead. They do not enclose materials which are inter-related and reactive enough to independently provide the collection of functions required for reproduction. Proteins are substances which coalesce from metallic or other ions. They are required for standardized elemental transformations to take place through processes which share similarities to catalytic induced chemical reactions, ongoing accumulative or reducing functions or energy producing interactions.

They are like the lead plates in a lead-acid battery: remove them form the battery and the capacity for power generation halts. Yet with their presence and an interconnectiveness between the protein mineral base (itself in contact with nucleic acids) and another biological unit, electrical power excitation can be transferred to the secondary unit and there potentially initiate or sustain new catalytic or other dynamic biochemical activity.

Proteins will become important to biological function yet they are not part of the biological structure. That is, minerals act to enable biological function. Viruses represent a protein-coated membrane enclosing nucleic acids. They are like a battery without a motor to drive. They are biological units rather than systems.

A typical virus is composed of DNA (deoxyribonucleic acid), or RNA (ribonucleic acid) surrounded by a protein coat. Both DNA and RNA are molecules that contain genetic (standardized, consistent, predictable strings of biochemical reactions) information in the form of a code. In effect, a virus is a packet of genetic material in a protective capsule. It is a plan without a purpose. That purpose will depend upon with what other biological units it can inter-relate and what the result of that inter-relation becomes.

Like an individual computer instruction which turns on or off specific hardware circuitry, the capability of a virus depends upon where its placement is within the "program" of the biological system. If it is in a position such that its function has no inter-relatedness to the other instructions surrounding it, its individual inertness remains unchanged: it has no influence; it goes unnoticed. If it does inter-relate with the programmed instructions in the subprograms which surround it, a contribution is made to the result of the activation of those programs.

Viruses are not cells in the sense that cells have a complex of function subprograms which enable a "system" of activities to be performed. Viruses are not quite cells and their forms may be various. Viruses may even take the form of crystals. Viruses have been found embedded within meteorites which have just landed on the Earth. This is how viruses first came to appear on the Earth.

Typically, humans consider life forms "alive" if they are capable of and appear to initiate movement and interaction with their surroundings. Humans largely consider any life form beyond this classification as either inert or dead. Viruses do not easily fit this perspective. Once formed, viruses simply exist until they come in contact with even more complex life forms: cells. That is, a virus appears to be just a nonliving combination of chemicals that can be frozen or crystallized with no harmful effects.

A virus may survive for years, even centuries or millions of years in this inactive state. It may even float around in space on specks of dust, unharmed by cosmic radiation; even having the potential to have its capability for interaction modified by such radiation much the same as cold temperatures tend to slow Earth-based chemical reactions compared to those taking place in very hot temperature environments. Viruses are more elemental structures than bacteria, fungi, and cells; they are normally found within each.

Viruses (Latin for "poison") are typically very small by human standards, most are much smaller than bacteria. The smallpox virus is one of the largest - 1/100,000 inch in diameter, about 1/4th the size of any bacterium. A hundred million crystallized polio viruses could cover the period at the end of this sentence. Remember this: Where there is life, there are viruses; the presence of a virus does not indicate a presence of life. Viruses are like an astronaut in suspended animation: nothing may change until the appropriate "key" activates them by including them in a dynamic system.

A virus is like a parasite in that it relies upon the existence and contact with a more complex lifeform to bring it to "life." Viruses contain a fundamental form of patterned intelligence within their biochemical structure. They may contain a strand or two of RNA, a basic building block of cellular lifeforms. When viruses come in contact with other lifeforms, they respond with behaviours which are predictable according to the reactive sequences which are part of their structure.

Viruses only interact with lifeforms which share some biochemical factor or element of composition. It is this "likeness" which both attracts the virus and the cell together and which fools the cell into inviting the virus into its abode. A virus cannot be readily identified until it encounters a lifeform with which it can interact; it is like a booby-trapped explosive waiting to be triggered by just the right stimulus.

Viruses cannot usually "live" long outside of a host.
The AIDS virus dies in 20 seconds. At the other extreme, no one has found how long a Marburg virus remains fully potent - at least 5 days in water - potentially hundreds of years if not exposed to sunlight. Ultraviolet light is effective at destroying what humans regard as life.

Every cell is surrounded by a membrane made of protein and fat molecules which form into particular shapes. All the materials that must enter a cell for it to grow, reproduce, and perform its function must dovetail into the shapes in the cell coating. No match, no entry. Viruses usually infect only one type of cell, the one which its shape unlocks the entry into. In some cases this function is much like that of recognizing the image of a friend at the door, unlocking the door and inviting the apparent friend inside.

A virus which has entered another lifeform which is advantageous to it, will begin to interact with the contents of the host. It will, as it were, feed upon the same food which the host utilizes - only it may do so in a more effective manner. As it feeds, the virus will utilize its new interactiveness to activate reaction processes within it which are patterns sometimes referred to as programs. One such program is the duplication of itself into more units: reproduction. The virus may multiply itself within a cell until practically the whole of the cell becomes occupied with virus and the internal cellular pressure becomes too great for the cellular membrane to contain: the "skin" breaks and the viruses flow out - in search of new contacts, leaving the original cell dead.

At other times, "recognition" is not as positive, yet it could be said that the doorkeeper is adequately deceived to neither open the door nor sound an alarm. This may be out of the patterned assumption on the doorkeeper's part that if the door is not unlocked, then the cell is protected. Some viruses are more aggressive than others and simply being allowed to "hang around" beside the cell can lead to tragedy. For these viruses, being allowed to attach themselves to the cell wall provides them with the opportunity to sabotage the cell. Finding a crack in the armor, the virus inserts a "needle" into the cell and injects genetic material through it.

The genetic material is like a group of new students or workers being registered at a day care centre or volunteering for work in an office or factory. Like regular personnel, they are familiarized with the routine and functions of the cell, and arrangements are made for their nourishment and housing. The difference between these students-workers and those of the cell is that these modify the functions of the cell, kill off (and consume) original cell workers, take over the factory, and, turn a colony into a new state in which viral progeny become the only inhabitants. Reproduction is much more rapid for the viral progeny and soon the new civilization has overpopulated the new utopia to the point where the cellular wall literally breaks open under the pressure. Free, the viruses now seek new cells to invade.

Described differently, with a different cell structure or style of viral "program", viruses may "bud" or project themselves through the host "skin" until they break through and fall outside the host. If the virus is "activated" sufficiently by the lack of discrimination of the host lifeform, by the lack of defence of the host lifeform, and by the energy (food) benefit of the host lifeform - it will reproduce quickly, exhaust the energies of the host, and, destroy the host. Destruction of the host - without another host close at hand - returns the virus to the immobile state. A virus can travel through space, survive entry through the Earth's atmosphere on a meteorite, and survive the impact and explosion which may be associated with landing: a virus is practically indestructible.

The human body is first protected against viral invasion by the outer layer of skin which is composed of dead cells. Viruses do not interact with dead matter. If the skin is stretched, torn, scratched, or torn - viruses can enter. Human saliva and tears are natural antiviral agents that protect the eye and mouth openings from viral intrusion. The mucus lining in the human nose and mouth traps viruses like a sticky paper traps dust or insects. In the bronchial tubes, and nose thousands of tiny hairs called cilia sweep upward, moving the mucous-trapped viruses into the throat where they are swallowed, or, down the nose, where discomfort encourages their being sneezed out or blown out. Tobacco smoke, air pollution, certain toxic chemicals, some drugs and dry air all serve to decrease the healthy activity of the cilia and increase the likelihood of local viruses gaining entry further into the human body than would be possible with a less compromised lifesystem. Most viruses can't survive stomach acid so those which are transported there usually die.

For those viruses which bypass or survive dead cells, cilia, saliva, tears, and stomach acid - the human immune system consisting of trillions of aggressive patrolling white "lymphocyte" cells serves to attack any form of life not genetically similar to their host human body. Some of these defensive cells are located in the blood stream; others are located in specific organs such as the tonsils, liver, spleen; still others are located in lymph nodes situated around the body at sites such as in the neck, chest, groin, and armpits. Special lymphocytes called "B" cells are biologically patterned to seek out any "foreign" lifeform and fashion antibodies to destroy it.

Some insects are capable of modifying the genetic code of their offspring when an attack is suspected. Within the human, the B-cells fashion new attack cells which are targeted to destroy only the genetic structure of specific invaders. Thus, antibodies for one virus are ineffective against a second type. Each new form of invader must have its own "personalized" opponent. This specialization limits the product of "general purpose" antigens which could mistakenly identify human cells as the enemy and attack them. Such a consequence of confusion, disorientation or desperation would result in the creation of a cancer. Ordinarily, it takes B-cells 5 to 7 days to generate enough antibodies to fight a virus. Then the person's health may begin to improve.

Viruses which have entered the body and entered target cells are protected from lymphocyte-generated antibodies. Now hidden behind the human cellular wall, the antibodies cannot sense the presence of the virus behind the acceptable biological code of the human cell. Another human "defender" cell, programmed in the thymus gland and called a "T"-cell, are capable of sensing viral cells within human cells. Having done so, they "target" the infected cell for attack by another form of immune system defender, the phagocyte, that is "cell eater." Phagocytes engulf and digest the "highlighted" viruses much as a scavenger would target a protein for food and eat it (the virus is covered in protein). 

Cells attacked by a virus release a chemical called interferon.
Tiny amounts of interferon inhibit the ability of most viruses to reproduce and generate more viruses. Interferon does not kill viruses, it just stops them from proliferating into greater numbers and higher densities.

Once T-cells and B-cells have bioengineered the appropriate phagocyte defenders, these new biological lifeform codes are retained in readiness for possible future invasions. In most cases, a subsequent invasion by the same form of virus will be met almost immediately by personalized antibodies. There is no 5-to-7 day delay this time. Residual antibody presence, from which new supplies are made may remain in the human body for years or even as long as the person stays alive. Vaccines are killed or weakened viruses which stimulate the production of antibodies and enable the construction of an immediate defence against highly destructive potential viral invaders.

In a first encounter with a virus or other agent which stimulates delayed hypersensitivity, it is often a race between multiplication of viruses and production of antibodies in the form of sensitized lymphocytes. In the case of some viruses this is truly a life-and-death race. When a second encounter with a specific type of virus takes place, there is already a significant population of sensitized lymphocytes in the circulation and these can fairly quickly multiply so that a high level of antibodies can be reached before the virus has multiplied very much.

2

http://www.ncbi.nlm.nih.gov/ICTV/nature.html
Families and Genera of Viruses
Listed According to the Nature of the Genome (table)
The International Committee on Taxonomy of Viruses

very extensive table, in brief ...

Bacterial Viruses

Fungal Viruses

Plant Viruses

Invertebrate Viruses

Vertebrate Viruses

3

http://www.stanford.edu/~siegelr/virusfam.html
Virus
Stanford University

The Human Viral Families

DNA viruses

Pox

Herpes

Adeno

Papova

Parvo

Hepadna

RNA viruses

Picorna

Calici

Astro

Toga

Flavi

Corona

Paramyxo

Orthomyxo

Bunya

Arena

Rhabdo

Filo

Borna

Reo

Retro

4

http://depts.washington.edu/labweb/cs/viro.html
Virology
Washington University

... Viral Culture-Screen
Specimens that are submitted for a Viral culture screen are processed to detect Influenza, Parainfluenza, Mumps, Measles, Adenovirus, Rhinovirus, Respiratory Syncytial Virus (RSV), Echoviruses, Coxsackie, Polio and Herpes group Viruses. This is the test to request to maximize the ability to detect a viral infection. Appropriate specimens include throat swabs, nasopharyngeal swabs, nasal washes, rectal swabs, conjunctival swabs, lesion swabs, urine, CSF and tissues. Positive culture results are called the day the virus is detected. All positive cultures are confirmed by either FA or neutralization. Order "Viral Culture: Screen". ...

CMV Rapid Assay
For rapid detection of Cytomegalovirus (CMV), the specimen is inoculated by centrifugation onto a monolayer and stained for CMV antigen with monoclonal antibody at 48 and 96 hours post inoculation in addition to standard viral culture. Swabs (in Viral Transport Media), body fluids or tissue can be submitted. This test is recommended for all lung biopsies, bronchoalveolar lavage specimens and tissue specimens. In addition, a 24-hour rapid stain can be ordered. This test is recommended for BAL from immunocompromised patients. ...

Viral Culture-Herpes Group
Specimens submitted for this assay are processed primarily for the identification of Herpes simplex type 1 (HSV-1), Herpes simplex type 2 (HSV-2), Cytomegalovirus (CMV) and Varicella Zoster Virus (VZV). Appropriate specimens include lesions, genital sites, conjunctival swabs, throat swabs, rectal swabs, buffy coats (EDTA or heparinized), or tissues. First morning voids of urine are more concentrated and contain the highest titers of virus. ...

Specimens to rule out HSV-1 or HSV-2 are read daily for 5 days, and then every other day before being reported as negative after 14 days of observation. CMV and VZV are slow growing viruses and their cultures are maintained up to 28 days before being reported. All negative Herpes group cultures receive a preliminary report after 5 days incubation. Positive culture results are called to the ordering location or physician as soon as virus is detected. All positive cultures are confirmed by FA and HSV isolates are subtyped with monoclonal antisera.

Clostridium difficile Toxin Assay
Patients suspected of having antibiotic-associated colitis should have 5-10 grams of fresh stool sent to the Virology Laboratory for a Clostridium difficile toxin assay. The stool should be placed in a sterile container. Rectal swabs are NOT acceptable. The stool can be stored at 4°C for 48 hours or frozen immediately at -20°C if transportation is delayed. The assay is set up daily. A preliminary result is ready 24 hours after inoculation and the final report is given at 48 hours. ...

Chlamydia trachomatis Culture
Chlamydia Transport Medium differs from Viral Transport Medium; they are not interchangeable. Wooden swabs and calcium alginate swabs inhibit the growth of Chlamydia and should never be used to culture for Chlamydia. A nasopharyngeal swab obtained from both sides of the posterior pharynx is the optimal method for culturing infants suspected of having infant pneumonia syndrome. For infants with conjunctivitis, swab the lower conjunctive of both eyes. Tissues can also be cultured by having either the swab or biopsy dropped into the Chlamydia Transport Medium.

The optimal genital sites for chlamydia isolation are the urethra in men and the urethra and/or endocervix in women (separate swabs can be combined for culture). Rectal swabs should be collected from homosexual and bisexual males. Chlamydia specimens can be stored at 4°C for 48 hours without significant loss of titer or immediately frozen at -70°C if transportation is delayed. Avoid freezing at -4°C or -20°C. ...

BK Virus PCR assay
BK virus polymerase chain reaction detects the presence of BK virus DNA in a variety of clinical specimens. 60 to 80% of adults in the United States have antibody to BK virus, and BK virus DNA can occasionally be found in the urine. The clinical significance of BK viruria is controversial. BK viruria may be associated with late-onset hemorrhagic cystitis after bone marrow transplantation, although BK viruria does not invariably lead to cystitis. Interpretation of BK virus PCR therefore requires substantial clinical and laboratory experience. ...

Enterovirus by PCR
Enterovirus is the most common cause of aseptic meningitis. PCR detection of enterovirus RNA in CSF is the most rapid way to diagnosis enteroviral meningitis. The enteroviruses detected by this assay include polio, coxsackie A and B, and Echoviruses. Since this assay also picks up rhinoviruses, a rhinovirus specific assay will be set up if the specimen is positive by our enterovirus PCR assay. ...

Herpesvirus PCR assays
Herpesvirus polymerase chain reaction assays can detect the presence of HSV-1 and HSV-2, CMV, EBV, HHV6, HHV8 or VZV DNA in a variety of clinical specimens. The clinical significance of finding DNA varies, for instance, detecting 10 HSV genomes in saliva from a healthy adult has little importance because most adults are infected with HSV-1 and low levels of viral excretion have no proven relationship to clinically apparent disease. In contrast, even a few HSV genomes in cerebral spinal fluid (CSF) from a neonate with convulsions probably indicates a life-threatening HSV encephalitis because neonates do not normally have HSV in CSF. ...

JC Virus PCR assay
JC virus is a papovirus belonging to the polyoma family. The virus infects the myelin and causes the disease known as progressive multifocal leukoencephalopathy (PML). The concordance of PCR detection of JCV in spinal fluid with clinical diagnosis of PML is at minimum 92%. Thus, the examination of CSF for JCV by PCR is a useful test for confirming the diagnosis of PML. JC virus PCR test will be run on the same schedule as the Herpesvirus PCR assays. ...

The Cytomegalovirus IgM assay detects both IgM and IgG to CMV. The CMV IgM assay can distinguish acute primary infection from reactivation and distinguish passively transferred maternal IgG from neonatal IgM in infants. The CMV IgM assay is run once each week.

Epstein-Barr (EBV) Battery
Epstein Barr Virus (EBV) antibody assays include IgG and IgM antibodies to EBV viral capsid antigen (VCA) and antibodies to EBV nuclear antigen (EBN). Testing is performed twice a week. An interpretive report is included.

Hepatitis Serologies
Hepatitis A is a fecal-oral transmitted infection often acquired through contaminated food. Hepatitis A Virus or antigen detection is not practical because viral shedding has ceased in most patients before clinical symptoms appear. ... IgM antibody tests are performed on all reactive specimens. Hepatitis A IgM indicates acute infection. ...

Measles/Mumps
Measles or mumps immune status is determined on a single serum by EIA. Measles and mumps titers require acute & convalescent paired serum and are forwarded to the appropriate reference laboratory.

Rubella (German Measles)
Rubella Immune Status is an EIA screen for Rubella antibodies, and is done three times a week. A positive result indicates a past rubella infection or immunization. For acute infections, a Rubella IgM is recommended. This is the preferred method of diagnosing a Rubella infection because the virus is very unstable and difficult to culture.

Varicella Zoster Virus (VZV) Antibody
The Varicella Zoster Virus (VZV) antibody screen is a qualitative assay to determine the immune status of individual with respect to VZV. It is particularly useful for immunocompromised or pregnant patients who are at risk of developing severe Varicella disease and who, if negative, may be candidates for Varicella Zoster Immune Globulin (VZIG). It is also useful for screening health care providers who may be exposed to the disease. VZIG must be given within 72 hours of exposure. ...

Pericarditis - CNS Syndrome Serologies
Coxsackie B1-6
Coxsackie B related myocarditis or pericarditis occurs after viral shedding from throat or rectum has ceased. Therefore, the best way to diagnose this infection is with acute and convalescent sera drawn 2 weeks apart. Our test assays neutralizing antibodies to Coxsackie B1 through B6. ...

"TORCH" screens are not available through the Virology Laboratory. Viral serologies on babies are not generally useful unless they measure IgM antibodies; IgG assays will only reflect maternal serostatus. For the "TORCH" organisms, reliable IgM assays are available for rubella and CMV and Toxoplasma (Microbiology section). Herpes, CMV and enteroviruses are best diagnosed by culture of babies' urine, throat, rectum or conjunctiva.

Enterovirus serologies (except Coxsackie B) are not performed because there are no common antigens among the 31 serotypes. Throat, rectal and occasionally CSF cultures are recommended. Most enteroviruses are shed for 2 to 4 weeks following onset of disease. ...

5

Anti-viral herbals commonly quoted.
various sources

A* http://www.healthlines.co.uk/TINCTURES/Tinctures.html
Herbal Tinctures and Oils
FROM HOWBARROW ORGANIC FARM

B* http://www.chclibrary.org/micromed/00050960.html
Herbal Remedies
CHC Wausau Hospital's Medical Library and Patient Education Center

C* http://critters.www4.50megs.com/herbs.htm
The Healing Power of Herbs

D* http://www.modernherbalist.com/list-viral-products.html
Modern Herbalist

• Alpha Lipoic Acid
  In 1991, researchers showed for the first time the synergistic action of the antioxidants vitamin E, vitamin C, Alpha Lipoic Acid and glutathione. This so called "antioxidant network" ensures comprehensive protection from free radicals. Production of the free radical species of oxygen is a normal mechanism that the body's immune system uses to harm and kill potentially infectious microbes and viruses. To do this, immune cells are targeted to the environment where these foreign materials are located and perform their toxic, damaging free radical reactions in the micro environment. For example, this is very important in the early stages of wound healing.

  As long as the ratio of oxidants to antioxidants remains in balance, the negative effects of free radicals are kept under control. When that balance is upset by overexposure to the sun, smoking, heavy metals toxicity, radioactivity, or other lifestyle or environmental factors, the antioxidants produced by the body simply can't cope with the sudden increase of free radicals.

  Alpha Lipoic Acid is a small molecule that is soluble in both water and fat. This is significant because water soluble antioxidant nutrients (vitamin C for example) are found within the cell and fat soluble antioxidants (vitamin E for example) are found on the cell membrane. Because Alpha Lipoic Acid works both inside the cell and at the membrane level, you get dual protection. At the membrane level you get protection before free radicals enter the cell. Any free radicals that makes it past the first line of protection are combated right in the cell itself.

  Alpha Lipoic Acid differs from glutathione which is the other major (sulfur containing) antioxidant in the body. Since glutathione cannot be transported across the intestinal tract, glutathione levels cannot be increased by dietary means to augment the antioxidant defence from this substance. In contrast, Alpha Lipoic Acid which is readily absorbed and has, in fact, been found to increase glutathione levels as the result of its ability to regenerate glutathione back to its potent antioxidant form.

  Alpha Lipoic Acid is present in the leaves of plants containing mitochondria and nonphotosynthetic plant tissues, such as potatoes. Another source which is very high in mitochondria is red meat. This is probably the richest source of naturally-occurring Alpha Lipoic Acid. Dietary supplementation of Alpha Lipoic Acid may be especially important for vegetarians and those cutting down on red meat consumption.
  
  
  

• A* Calendula (Marigold)
  Marigold is antiseptic, antifungal and antibacterial making it excellent for healing a wide range of conditions. On the skin it can be used in the treatment of eczema and thrush, and is also excellent first aid for burns, scalds and stings as well as any wounds where the skin is broken. An infusion of marigold can be used to treat inflamed or ulcerated conditions such as gastritis, gastric or duodenal ulcers and, as it stimulates the flow of bile it is a useful digestive remedy. It can also be used to allay painful periods and help regulate the menstrual cycle.
  
  
  

• Cinnamon
  
  
  

• C* Echinacea (Purple Coneflower)
  ... one of the finest blood cleansers, especially for skin problems associated with impure blood, such as boils or abscesses. .. As an immune system enhancer, Echinacea has been shown to stimulate the production of white blood cells, which fight infection and also has anti-viral properties.
  
  
  

• D* ENGYSTOLŪ N
  Effective German homeopathic formulation for the treatment of acute and chronic viral symptoms. For the temporary relief of fever, malaise, body ache and joint pain.
  
  
  

• B* Garlic
  Comparing a natural antibiotic, like garlic, with a synthetic dose of penicillin reveals that synthetic antibiotics work well but also indiscriminately, killing even the good bacteria in the body's gastrointestinal system. Garlic, on the other hand, actually stimulates beneficial bacteria to work better.

  Garlic is reported to be more effective than penicillin against typhus disease, and works well against strep, staph bacteria, and the organisms responsible for cholera, dysentery and enteritis. The irritating quality of garlic oil, readily absorbed into the bloodstream, may explain its use for respiratory problems by opening up lungs and bronchial tubes.

  It is also extremely effective in dissolving and cleansing cholesterol from the blood stream; it stimulates the digestive tract; it kills worms, parasites and harmful bacteria; it normalizes blood pressure and reduces fever, gas & cramps; it used by athletes for increasing physical strength & energy. Garlic has also been found to inhibit tumor cell formation.
  
  
  

• C* Ginger
  Aids in fighting colds (viruses), colitis, digestive disorders, flu & gas; it helps increase the secretion of saliva; is excellent for the circulatory system and helps increase stamina.
  
  
  

• Grapefruit seed extract
  
  
  

• A* Melissa (Lemon Balm)
  Lemon Balm can be used to induce sweats making it useful for treating colds and flu, it also has antiviral properties which are effective against mumps, cold sores and other viral infections. It is recommended for nervousness, depression, nervous headaches and insomnia having a sedative effect but lifting the spirits.
  
  
  

• C* Licorice (Glycyrrhiza glabra)
  Homeopathic use of licorice for gastric irritation dates back to the first century. Today, herbal preparations are used to treat stomach and intestinal ulcers, lower acid levels and coat the stomach wall with a protective gel. Rarely used alone, it is a common component of many herbal teas as mild laxative, a diuretic, and for flatulence. It has also been known to relieve rheumatism and arthritis, regulate low blood sugar, and is effective for Addison's disease. The root extract produces mild estrogenic effects, and it has proven useful in treating symptoms of menopause, regulating menstruation, and relieving menstrual cramps.

  The main ingredient glycyrrhizin has also been studied for it's anti-viral properties in the treatment of AIDS. In clinical trials in Japan it prevented progression of the HIV virus by inhibiting cell infection and inducing interferon activity. Glycyrrhizin also encourages the production of hormones such as hydrocortisone which give it anti-inflammatory properties. Like cortisone it can relieve arthritic and allergy symptoms, without the side effects.
  
  
  

• C* Neem
  The leaf and oil of the Neem tree contain compounds impressive therapeutic qualities:

   *Antiviral            *Antipyretic         *Antifungal
   *Antibacterial        *Analgesic           *Anti-inflammatory
   *Anti-tumor           *Anthelmintic        *Immune stimulant
   *Antimicrobial        *Antiemetic
  

  Teeth And Gums
  It is estimated that over 90% of the U.S. adult population has some type of gum (periodontal) disease. Mouth infections, tooth decay, bleeding and sore gums have been treated successfully with the daily application of Neem oil. Some people have reported a total reversal of gum disease after using Neem for only a few months.

  Daily Care:
  Brush teeth as you normally would, then..... put Neem Oil 1-2 drops & Carvacrol Oil 1-2 drops on wet tooth brush and brush teeth, gums and tongue. Do not rinse. You may drink water, as needed. Most bacterial infections begin in the mouth.
  
  
  

• D* Olive Leaf Extract
  Olive leaf extract contains important antiviral, antifungal, antibacterial,l antioxidant, hypoglycemic (blood sugar lowering) and vaso-diliatory effects. Very helpful in viral illness and candida infection.
  
  
  

• D* Wobenzym-N
  Systemic enzymes have been found to be effective in the treatment of inflammation & infection due to bacteria, fungus, yeast or virus. Also very useful in treatment of joint disorders, cardio-vascular problems and traumatic injury. A high potency combination of pancreatin, bromelain, papain, rutin, trypsin, chymotrypsin.
  
  
  

• Zinc
  This mineral is known to be involved in the maintenance of most cells and contributes to an anti-viral defence.

Viruses are encouraged in % of population to reactivate by

• 100% - bacterial infections;
• 098% - stresses, change, conflict;
• 091% - new virus infections;
• 080% - energy blocks (+/- 7%);
• 008% - strong imprinting.

ONE of the above factors is mandatory PLUS at least ONE supporting factor.

Health improvement is a CHANGE for a person who has been chronically ill. One may feel worse and have more and/or different symptoms if one is getting BETTER from their chronic illness AND one or more dormant viruses have reactivated.

One's Reptilian Structure will benefit from being reassured that getting BETTER IS A POSITIVE. Knowing of this dynamic, using affirmations, and, reading Spiritual Principles, as determined relevant by muscle testing or Spiritual Guidance can assist this improvement.

Dormant viruses are like oil slicks within your cells.
That is, like oil on the surface of water they form a unified structure with boundaries held together by surface tension. Detergents include surfactants which break up surface tension and allow the oil and water to mix. In this way, the integrity of the oil structure is destroyed and the small pieces left are captured by other detergent ingredients and become able to be removed and excluded. This can also happen with viruses.

First, our own cell membranes must be weakened.
This allows the dormant virus to emerge as well other things, like heavy metals, which are normally held tightly in our cells.

Secondly, outside the cell, the virus boundary can now be weakened so that Reptilian Structure will recognize it and disperse and excrete the pieces of it.