What are the Benefits of Ozone Therapy?
- Ozone strengthens your immune system.
- Ozone kills bacteria and viruses on contact.
- Ozone increases the oxygen level of your cells.
- Ozone detoxifies your body.
- Ozone reduces inflammation.
- Ozone can kill cancer cells.
- Ozone is anti-aging.
- Ozone increases energy.
- Ozone reduces acidity.
Conditions that may benefit from treatment with Ozone Therapy include:
- Meniscal tears/joint disorders
- Shingles (Herpes zoster) and Herpes Simplex
- Herniated Discs
- Diabetic ulcers and venous stasis
- Allergies & chronic sinusitis
- Lyme disease
- Alzheimer’s, senile dementia
- Autoimmune diseases
- Colitis and Crohn’s
- Vaginal infections
- Chronic hepatitis
- Chronic Fatigue Syndrome
- Candidiasis and many more conditions
Why Ozone Therapy?
Because scientific studies have proven that Ozone, properly introduced into the body in repeated applications inactivates viruses, bacteria, fungi, protozoa and carcinomas in diseased cells! *
How Does Ozone Therapy Work?
Ozone therapy has been in use for many years by thousands of West German doctors who claim, in hundreds of scientific and clinical studies, that they are able to inactivate AIDS and other viruses and cancer through ozone therapy. They explain that diseased cells have a lowered enzyme count in their cell wall or ‘lipid envelope’.
Looking at a diseased cell electrochemically, the first thing that differentiates it from normal cells is that the protein coating that surrounds it is contoured distinctly. The disease that has invaded the cell is parasitical, drawing off the cellular electricity or ‘life force’ of its host. This creates ‘cell stress’ and under these conditions, the cell can only manufacture a substandard protein coating for itself. When ozone is introduced into the blood in correct, stable concentrations ** it is immediately converted into hydroxyperoxides and other beneficial free radical scavengers. ***
Ozone Is Safe and Non-Toxic
Medical ozone (the correct term is triatomic oxygen, but for simplicity we will call it medical ozone) is completely safe and non-toxic to humans when administered responsibly with precise technology. It is extremely important that the proper ozone generator be used to generate the ozone. One must ensure that the ozone is clean, pure, and free of contaminants. This is only possible if the ozone only touches a glass electrode (never metal or ceramic) while inside the ozone generator, and only possible if the tubing and fittings inside the electrode are 100% ozone resistant. If the ozone touches metal, plastic, rubber, or other materials that can be oxidized by the ozone, the byproducts of the breakdown of these materials will travel with the ozone and contaminate the ozone.
It is not meant to be breathed directly, although small amounts in the air, in fact, a sterilizing technique. When introduced into the blood through rectal/vaginal insufflation or major autohemotherapy it has been shown to be completely safe even when a dosage many times greater than the proposed human dosage is administered.
Here are extracts from the extensive studies proving the non-toxicity of medical ozone:
- An animal model treated with medical ozone in a manner analogous to the proposed human treatment regime at the Long Island College of Pharmacy revealed no toxicity at concentrations up to ten times the dose proposed in man.
- Research studies: “Effects of long-term exposure to low levels of ozone: a review.” C.W. Melton (Aviation, Space & Environmental)
- “Ozone: An overview of its toxicity in man and animals.” D. Menzel (Toxicol & Environ Health 1984)
- “Toxicity of Ozone.” S. Mittler. M. King. B. Burkhardt (AMA Arch Ind. 1957)
UVBI and Ozone (Major AutoHeme)
UVBI came about in the early 1930s. At that time, polio was the scourge of young people and American Medicine had little to offer those stricken. Today polio is a non-issue, as a result of polio vaccination. As kids we received attenuated (lethally injured) polio virus, to which our immune system develops effective immunity. UVBI was invented by Emmitt Knott, an American engineer. The ex vivo (outside the body) antimicrobial effects of UV light had been known for years. Knott reasoned that exposure of a portion of one’s blood to UV energy would lead to an in vivo (within the body) enhanced immune response. Knott demonstrated a benefit in animals. The first human to be treated (1933) was a young woman dying of sepsis. All else had failed, but UVBI didn’t; she made a full recovery. The second patient recovered from a brain abscess. Doctors got excited; more patients were treated, and by the late 1940s 1000s of patients had been successfully treated and over 100 papers published. UVBI worked where all else had failed. High levels of success with the use of UVBI in bacterial and viral infections (including polio) were reported. Surgeons noted a smoother post-op course when UVBI was applied pre-operatively. Hypoxic patients treated with UVBI demonstrated improved blood and tissue oxygenation that lasted for weeks. Applications in Military Medicine were found; UVBI improves tolerance to hypoxia in flyers and tolerance to bends in divers.
In the ‘50s, new, patentable antibiotics came out and the attention of American physicians was shifted away from low-cost, non-patentable UVBI and towards the new pharmaceuticals, for which research money was available (same story as EECP). UVBI remained in use in Germany and within the Soviet bloc, where 100s of additional papers were published. We now have drug resistant bacteria (bacteria cannot become UV resistant). Air travel brings with it the potential for rapid dissemination of viral agents to which none of us are immune.
Ultraviolet Blood Irradiation (UVBI) involves the closed circuit, ex vivo exposure of less than 1/20th of your bloodstream to ultraviolet light. Rapidly dividing or metabolically overactive blood components (bacteria, parasites, and viruses) will absorb excessive ultraviolet energy and sustain DNA/RNA damage. Resting white cells will absorb less energy but will use this energy to up regulate their oxidative anti-microbial defense mechanisms. Infused back into your circulation will be dead/attenuated microbes (which act like a vaccine – UVBI was first used to treat polio) and physiologically up regulated immune cells. Thus, UVBI is effective (multiple papers to prove this) in human bacterial and viral infection. Abnormally activated immune cells, such as those involved in asthma and autoimmune conditions, will also absorb excessive energy; thus, a benefit of UVBI in asthma and (likely) other auto-immune conditions. The oxygen binding determinant of hemoglobin (2,3-DPG) is altered, such that blood and tissue oxygenation improve. While only a small portion of your circulation receives direct ultraviolet energy, these cells will release photons of energy to the remaining cells of your body (termed secondary emanation), so your entire body is treated. Autonomic nervous system function is affected, leading to peripheral vasodilation. Toxins are inactivated; thus, UVBI rapidly clears the “toxicity” of infection and may be useful in the treatment of spider and snake bites. UVBI has been used successfully in wound healing and in speeding recovery from surgery (given either pre or post-op). A German study demonstrated a symptomatic benefit in peripheral vascular disease, and American case reports described favorable affects in CV conditions.
So why isn’t UVBI in widespread use today? UVBI is FDA allowed, but the machines are not patentable. There is no financial incentive for any entity to fund UVBI research. UVBI just does not fit in with the way we do Medicine in the US. To quote Robert Rowan MD UVBI is “The Cure that Time Forgot”. Now it is our time to bring this low cost, low risk treatment back.
Conditions that Typically Benefit from UVBI and Ozone
Delayed Wound Healing
Neutralizes Infectious Toxins
Toxemia of Pregnancy
Prep for High Risk Surgery
Reduces Blood Viscosity
Conditions that Might Benefit from UVBI and Ozone
Coronary Artery Disease
Roberts MD FACC FAARFM 2/13/18
Ozone with UVBI Therapy
IV Ozone therapy is a natural, safe, and powerful therapy that can be used to promote healthy aging and treat many ailments and diseases. Ozone therapy increases the amount of oxygen in the body to improve overall bodily function. Ozone is a potent oxidant that increases circulation and blood flow, optimizes cellular oxygen metabolism, decreases inflammation and signs of aging, detoxifies the liver, treats chronic infections, and stimulates the immune system.
Ozone has antimicrobial properties that can cleanse the blood and clear out infections, including those that are notoriously hard to treat. In addition to killing pathogenic bacteria and other pathogens, ozone strengthens the body’s natural immune system by increasing the production of white blood cells and modulating immune activity.
Ozone treatment is also an effective tool in infection prevention. Additionally, while ozone kills pathogenic bacteria, it does not disrupt the beneficial flora in the body, nor does it kill off healthy cells.
Ozone is an effective treatment for:
Viruses, Lyme Disease and co-infections, Mold and mycotoxins, Bacterial infections, Wound healing, Parasites, Dental infections, Acne, Eczema, and other chronic infections.
When utilizing ozone along with UVBI therapy you create an overall stronger, healthier, result than using one or the other alone. Let me repeat from above: The oxygen binding determinant of hemoglobin (2,3-DPG) is altered, such that blood and tissue oxygenation improve. While only a small portion of your circulation receives direct ultraviolet energy with ozone, these cells will release photons of energy to the remaining cells of your body (termed secondary emanation), so your entire body is treated.
Ozone works on biological systems to strengthen them towards health, regardless of stressors. Because chronic conditions are complicated and often difficult to cure it’s because more than one biological system is off, and ozone can treat all of them.
At Transformational Medicine we use both ozone and UVB together because daily, we see how much more benefit is provided to the patient.