Omnivir is a medical device that generates humidified active oxygen in the form of a very energetic oxygen singlet (O) , pure oxygen (O2) and triatomic oxygen (O3, also known as medical ozone). Omnivir is used at home or clinics to care for HIV by reducing viral load, boosting immune and detoxifying the body.
How Active Oxygen works on HIV and Immune System: Active Oxygen deactivates and eventually kills HIV by destroying its protective skin. Ozone's destructiveness nature on HIV, virus and bacteria is partly attributed to the oxidation of unsaturated bonds in the phospholipids and lipoprotein architecture of the bacteria, viruses. The oxidation generates hydro peroxides, which are transformed to peroxyl and hydroxyl radicals and to other reactive species, including aldehydes. Peroxyl radicals attack proteins, and hydroxyl radicals induce disruptive structural changes in cell membranes. The reactive oxygen intermediates also contribute to the inactivation of viral reverse transcriptase. In order of preference, ozone reacts with polyunsaturated fatty acids (PUFA), antioxidants such as ascorbic and uric acids, thiol compounds with -SH groups such as cysteine, reduced glutathione (GSH) and albumin All of these compounds act as electron donor and undergo oxidation. Ozone reacts with body fluids forming moles of hydrogen peroxide (included among reactive oxygen species, ROS) and moles of lipid oxidation products (LOPs) The fundamental ROS molecule is hydrogen peroxide, which is a non-radical oxidant able to act as an ozone messenger responsible for eliciting several biological and therapeutic effects. Hydrogen Peroxide already exists in human cells and its the key chemical on fighting infections, e.g. viruses and bacteria. The ozone bio-oxidative process is therefore characterized by the formation of ROS and LOPs acting in two phases. ROS are acting immediately and disappear (early and short-acting messengers), LOPs, via the circulation, distribute throughout the tissues and eventually only a few molecules bind to cell receptors . In fact of ozone returns to normal within half an hour and the oxidized compounds such as dehydroascorbate are efficiently recycled back to ascorbic acid. H2O2 diffuses easily from the plasma into the cells and its sudden appearance in the cytoplasm represents the triggering stimulus: depending upon the cell type, different biochemical pathways can be concurrently activated in erythrocytes, leukocytes and platelets resulting in numerous biological effects.
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At right concentration, medical ozone kills 99.999% lipid viruses and bacteria in the tests tube, water and in the air. Here is a list of opportunistic pathogens susceptible to the antiviral and antibacterial power of ozone therapy: herpes viridae, simplex, varicella-zoster, kaposi sarcoma, epstein - barr, influenza, hepatitis.
Ozone also acts as an enhancer of the immune system by activating neutrophils and stimulating the synthesis of some cytokines. The by product of ozone, hydrogen peroxide, which after entering into the cytoplasm of blood mononuclear cells (BMC) by oxidizing selected cysteines, activates a tyrosine kinase, which then phosphorylates the transcription factor nuclear factor ?B allowing the release of a heterodimer (p50+p65). This complex moves on to the nucleus and switches on some hundred genes eventually responsible for causing the synthesis of several proteins, among which are the acute-phase reactants and numerous interleukins. Once the ozonated leukocytes return to the circulation, they home in lymphoid microenvironments and successively release cytokines acting in a paracrine fashion on neighbouring cells with a possible reactivation of a depressed immune system.
Active Oxygen Success on HIV/AIDS: This medical gas has been in use for a long time mostly in hospitals and by physicians across the world. Physicians report 99.9% success rate on HIV patients, also remission of the condition in most cases. Doctors across the world claims to have cured HIV on more than 500 patients using a rigorous and very expensive ($25,000) protocol which included Active Oxygen IV Therapy as the main treatment. There are more than 5 US and International patents for research to cure HIV using active oxygen/ozone, none have been put on the market due to production and regulatory costs.
Active Oxygen Therapy is used in major countries i.e. UK, Malaysia, China, USA, Japan, Italy, Russia, South Africa, Germany , France, Cuba, Canada, Ireland, Europe, India, Americas. Click Here to see a list of doctors offering the cheapest (average $300/month) active oxygen rectal therapy worldwide.
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Acquired Immune Deficiency syndrome or AIDS is a collection of symptoms and infections resulting from the specific damage to the immune system caused by the human immunodeficiency virus. The late stage of the condition leaves individuals prone to opportunistic infections and tumors. Although treatments for AIDS and HIV exist to slow the virus's progression, but, there is no known cure.
There is currently no vaccine or cure for HIV or AIDS. The only known method of prevention are based on avoiding exposure to the virus or failing that an antiretroviral treatment directly after a highly significant exposure, called post-exposure prophylaxis.
Well current treatment for HIV infection consists of highly active antiretroviral therapy, also known as HAART. This has been highly beneficial to many HIV-infected individuals since its introduction in 1996. Current optimal HAART options consist of combinations consisting of at least three drugs belonging to at least two types, or "classes," of anti-retroviral agents. Typical regimens consist of two nucleoside analogue reverse transcriptase inhibitors plus either a protease inhibitor or a non-nucleoside reverse transcriptase inhibitor.
HAART allows the stabilization of the patient’s symptoms and viremia, but it neither cures the patient of HIV, nor alleviates the symptoms, and high levels of HIV-1, often HAART resistant, return once treatment is stopped. Moreover, it would take more than the lifetime of an individual to be cleared of HIV infection using HAART. Despite this, many HIV-infected individuals have experienced remarkable improvements in their general health and quality of life, which has led to the plummeting of HIV-associated morbidity and mortality.
In the absence of HAART, progression from HIV infection to AIDS occurs at a median of between nine to ten years and the median survival time after developing AIDS is only 9.2 months. HAART is thought to increase survival time by between 4 and 12 years. This average reflects the fact that for some patients and in many clinical cohorts this may be more than fifty percent of patients HAART achieves far less than optimal results. This is due to a variety of reasons such as medication intolerance/side effects, prior ineffective antiretroviral therapy and infection with a drug-resistant strain of HIV.
However, non-adherence and non-persistence with antiretroviral therapy is the major reason most individuals fail to get any benefit from and develop resistance to HAART. The reasons for non-adherence and non-persistence with HAART are varied and overlapping. Major psychosocial issues, such as poor access to medical care, inadequate social supports, psychiatric disease and drug abuse contribute to non-adherence. The complexity of these HAART regimens, whether due to pill number, dosing frequency, meal restrictions or other issues along with side effects that create intentional non-adherence also has a weighty impact. The side effects include lipodystrophy, dyslipidaemia, insulin resistance, an increase in cardiovascular risks and birth defects.
Thus, it becomes clear that despite the widespread use of complementary and alternative medicine by people living with HIV/AIDS, the effectiveness of the therapy has not been established yet.
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