How Doctors Cured Cancer and AIDs

[Magicman]

More Doctors Get Rid of HIV THROUGH OZONE THERAPY

Michael T.F. Carpendale, M.D., Chief of Medicine and Research Services at the Veterans Administration Hospital in San Francisco and Professor at the University of California School of Medicine, San Francisco, and his associate, Dr. Joel K. Freeberg.


NA: In-vitro studies to evaluate the ability of ozone to kill the HIV virus in the test tube were undertaken by scientists in the United States, Russia and Canada. The first researchers in the world to prove that ozone can inactivate HIV were Michael T.F. Carpendale, M.D., Chief of Medicine and Research Services at the Veterans Administration Hospital in San Francisco and Professor at the University of California School of Medicine, San Francisco, and his associate, Dr. Joel K. Freeberg of the Veterans Administration Hospital.

They first presented their findings at the IV International Conference of AIDS in Stockholm, and later published their report in the peer-reviewed journal Antiviral Research. Carpendale and Freeberg showed that HIV could be 99 percent inactivated with only 0.5 micrograms of ozone per ml of serum, and completely inactivated by ozone concentrations of 4 micrograms per ml of serum. At the same time, these concentrations of ozone did not harm healthy cells.

Another in vitro study, supported in part by the U.S. Public Health Service and Medizone International, a manufacturer of a patented medical ozone delivery system, was reported in the October 1, 1991 issue of the medical journal Blood.
Using ozone generated from medical grade oxygen and delivered into a cultured cell medium of HIV-1, a team of four scientists from the SUNY Health Science Center in Syracuse, The Brooklyn Hospital and Merck Pharmaceutical, found that ozone deactivated the virus completely, yet without causing significant biological damage to non-infected cells.

In evaluating their findings with HIV, the researchers concluded:"The data indicate that the antiviral effects of ozone include viral particle disruption, reverse transcriptase inactivation, and/or a perturbation of the ability of the virus to bind its receptor to target cells."

In Russia, scientists at the Institute of Virusology in Moscow also used a concentration of 4 micrograms/ml of ozone on an infected culture containing HIV. Within minutes, the cell of the virus began to decompose and died. The researchers noted that: "Complete deactivation of the extra cell virus is achieved by putting gaseous ozone through the virus-containing liquid."

In 1992, a major study in Canada coordinated by the Surgeon General of the Canadian Armed Forces was undertaken to determine the ability of ozone to kill HIV, hepatitis and herpes viruses in blood used for transfusion. After a three-minute ozonation of serum spiked with one million HIV-1 particles per milliliter, a 100 percent deactivation of the virus was achieved.

Referring to this study during his interview in the video documentary "Ozone and the Politics of Medicine", Capt. (now Commander) Michael E. Shannon, a scientist and medical doctor with the Canadian Department of National Defense said: "...We are dealing not with concentrations that are toxic to the human, but are in fact concentrations of ozone that have been used in clinics in Germany for the last thirty years with thousands of patients without any evidence of any harm."

Despite the importance of the results which would indicate that simple ozonation of the blood supply would render it free of HIV, as well as herpes, hepatitis and other viruses the Canadian findings received little notice in the North American press.

 

[Magicman]

Please Take This Information, attach this as a note, copy and paste it and send this to your friend's list. Tell ALL your friends who want to stop AIDs/Cancer to do the same! We can change the world. Tell them to use O3 or Ozone Therapy. Send this to AIDs/Cancer Patients and doctors with a heart!
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Article you can download and send to others

http://www.scribd.com/doc/8788977/Ozone-Blood-Treatment-Cures-Aids-Victims-in-Germany



Everyone Watch these Videos to Find out the Truth


http://www.youtube.com/watch?v=8K7cmCp8T-M

http://www.youtube.com/watch?v=bVAMttloY_4

http://www.youtube.com/watch?v=r7lszrTJ3NM

Dr. Otto Warburg received the Nobel prize in 1931 for the discovery that unlike all other cells in the human body, cancer cells do not breathe oxygen. Cancer cells cannot survive in the presence of high levels of oxygen . There are many different types of successful treatments based on oxygenating the tissues, such as hydrogen peroxide therapy, hyperbaric oxygen tank, and blood ozonation. Chi machines are wonderful for increased circulation and oxygenation and there are several types of liquid oxygen drops that you can add to your water. It is helpful to understand the nature of acidity and alkalinity and why tissues deficient in oxygen are prone to cancer. Cancerous tissues are acidic, whereas healthy tissues are alkaline and the oxygen drop products help to raise your PH balance and oxygenate the body. Cancer cannot survive in an alkaline environment or in the presence of oxygen. If you PH is below 7 you are acidic and if it is above 7 your are alkaline. The body is designed to be slightly alkaline at a pH of 7.4. At a pH slightly above 7.4 cancer cells become dormant and at pH 8.5 cancer cells will die. I suggest that you test your PH with Litmus paper so you know where you are.


How Ozone Works With AIDS?


The 13 Major Effects of Cancer Oxygen Ozone on the Human Body - By Dr. Frank Shallenberger

[Considered one of the leading authorities on medical ozone, Dr. Shallenberger has done important work to support the hypothesis that ozone can have long-term positive effects on AIDS. He has also conducted workshops on the proper application of medical ozone at an International Ozone Symposium in Texas. He successfully treats patients with medical ozone via Major Autohemotherapy. The thirteen physiological effects are list below and are accompanied by a brief explanation.]

1. Ozone stimulates the production of white blood cells. These cells protect the body from viruses, bacteria, fungi and cancer. Deprived of oxygen, these cells malfunction. They fail to eliminate invaders and even turn against normal, healthy cells (allergic reactions). Ozone significantly raises the oxygen levels in the blood for long periods after ozone administration; as a result, allergies have a tendency to become desensitized.

2. Interferon levels are significantly increased. Interferons are globular proteins. Interferons orchestrate every aspect of the immune system. Some interferons are produced by cells infected by viruses. These interferons warn adjacent, healthy cells of the likelihood of infection; in turn, they are rendered nonpermissive host cells. In other words, they inhibit viral replication. Other interferons are produced in the muscles, connective tissue and by white blood cells. Levels of gamma interferon can be elevated 400-900% by ozone. This interferon is involved in the control of phagocytic cells that engulf and kill pathogens and abnormal cells. Interferons are FDA approved for the treatment of Chronic Hepatitis B and C, Genital Warts (caused by Papillomavirus, Hairy-cell Leukemia, Karposi’s Sarcoma, Relapsing-Remitting Multiple Sclerosis and Chronic Granulomatous Disease. Interferons are currently in clinical trials for Throat Warts (caused by Papillomavirus), HIV infection, Chronic Myelogenous Leukemia Leukemia, Non-Hodgkins Lymphoma, Colon tumors, Kidney tumors, Bladder Cancer, Malignant Melanoma, Basal Cell Carcinoma and Leishmaniasis. While levels induced by ozone remain safe, interferon levels that are FDA appoved (and in clinical trials) are extremely toxic.

3. Ozone stimulates the production of Tumor Necrosis Factor. TNF is produced by the body when a tumor is growing. The greater the mass of the tumor the more tumor necrosis factor is produced (up to a point). When a tumor has turned metastatic, cancer cells are breaking off and being carried away by the blood and lymph. This allows the tumor to take up residence elsewhere in the body; or in other words, divide its forces. These lone cancer cells have little chance of growing due to the TNF produced to inhibit the original tumor. When the tumor is removed surgically TNF levels drop dramatically and new tumors emerge from seemingly healthy tissue.

4. Ozone stimulates the secretion of IL-2. Interluekin-2 is one of the cornerstones of the immune system. It is secreted by T-helpers. In a process known as autostimulation, the IL-2 then binds to a receptor on the T-helper and causes it to produce more IL-2. Its main duty is to induce lymphocytes to differentiate and proliferate, yielding more T-helpers, T-suppressors, cytotoxic T’s, T-delayed’s and T-memory cells.

5. Ozone kills most bacteria at low concentrations. The metabolism of most bacteria is on average one-seventeenth as efficient as our own. Because of this, most cannot afford to produce disposable anti-oxidant enzymes such as catalase. Very few types of bacteria can live in an environment composed of more than two percent ozone.

6. Ozone is effective against all types of fungi. This includes systemic Candida albicans, athletes foot, molds, mildews, yeasts and even mushrooms.

7. Ozone fights viruses in a variety of ways. As discussed above, ozone also goes after the viral particles directly. The part of the virus most sensitive to oxidation is the “reproductive structure”. This is how the virions enter the cell. With this structure inactivated, the virus is essentially “dead”. Cells already infected have a natural weakness to ozone. Due to the metabolic burden of the infection the cells can no longer produce the enzymes necessary to deal with the ozone and repair the cell.

8. Ozone is antineoplastic. This means that ozone inhibits the growth of new tissue because rapidly dividing cells shift their priorities away from producing the enzymes needed to protect themselves from the ozone. Cancer cells are rapidly dividing cells and are inhibited by ozone.

9. Ozone oxidizes arterial plaque. It breaks down the nnnn plaque involved in both Arteriosclerosis and Arthrosclerosis. This means ozone has a tendency to clear blockages of large and even smaller vessels. This allows for better tissue oxygenation in deficient organs.

10. Ozone increases the flexibility and elasticity of red blood cells. When one views a red blood cell under a microscope, it looks like a disc. In the capillaries, where they pick-up (lungs) and release (tissue) oxygen, these discs stretch out into the shape of an oval or umbrella. This aids their passage through the tiny vessels and makes the exchange of gas more efficient. The increase in flexibility of the RBC’s allows oxygen levels to stay elevated for days, even weeks after treatment with ozone.

11. Ozone accelerates the Citric Acid Cycle. Also known as the Kreb’s Cycle or TCA Cycle, this is a very important step in the glycolisis of carbohydrate for energy. This takes place in the mitochonria of the cell. Most of the energy stored in glucose (sugar) is converted in this pathway.

12. Ozone makes the anti-oxidant enzyme system more efficient.

13. Ozone degrades petrochemicals. These chemicals have a potential to place a great burden on the immune system. They also worsen and even cause allergies and are detrimental to your long-term health.



How Ozone Works with Cancer?

Ozone Cancer Oxygen Therapy - Is It Safe?



1980 Jan - The German Medical Society for Ozone Therapy commissioned Marie Theresa Jacobs and Prof. Dr. Hergetbegan from the University Kilnikum Giessen and the Institute for Medical Statistics and Documentation of Giessen University to begin an inquiry entitled “Adverse Effects and Typical Complications In Ozone Therapy.” 2,815 questionnaires were sent out to all western German ozone therapists known by the Medical Society for Ozone Therapy (AGO, Arztliche Gesellschaft fur Ozontherapie). 884 went to physicians and 1931 to therapists.

1980 May - By now, The German Medical Society had collected 1,044 replies, or 37% of the total. The replies that were returned stated 384,775 patients were treated with ozone with a minimum of 5,579,238 applications. The side effect rate observed was only .000005 per application. The report also stated “The majority of adverse effects were caused by ignorance about ozone therapy (operator error)."

Even with this report, there are still some opponents who warn Ozone Therapy is unsafe. It is therefore wise to seek out an experienced ozone practitioner and to do further research into the pros and cons of this therapy.


Ozone Cancer Oxygen Therapy - Clinical Studies / Research

1. In 1980 laboratory studies by main stream cancer researchers at Washington University discovered ozone inhibited growth of lung, breast and uterine cancer cells in a dose dependent manner while healthy tissues were not damaged by ozone. Sweet F, Kao M S, Lee S. (Dept of obstetrics and Gynecology, Washington University. School of Medicine, St Louis) and W. Hagar (St Louis Air Pollution Control) publish in, Science Vol 209: 931-933, USA peer reviewed scientific journal, their study: Ozone Selectively Inhibits Human Cancer Cell Growth. They announce, Evidently the mechanisms for defense against ozone damage are impaired in human cancer cells. Cancer cells (lung, breast, uterine and dome trial) showed marked dose-dependent growth inhibition in o3 at .3 and .5 parts per million while the normal cells were not affected.

2. One of the first reports of successful cancer treatment with ozone using actual patients was reported, as mentioned above, by the German Dr Joachim Varro at the Sixth World Ozone Conference in 1983 and published in Medical Applications of Ozone (Ed. Julius LaRaus, Norwalk, Conn. pp 94-5). Dr Varro reported that patients experienced increased appetite, greater strength, higher rates of physical activity and reduction in pain. He stated that patients were 'free of metastases and tumour relapses for remarkably long periods of time; survival time could be prolonged, far exceeding the usual dubious prognoses, even in cases of inoperability, radiation resistance, or chemotherapy non-tolerance, and with improved quality of life. Most patients who had undergone the combination therapy shortly after surgery and radiation could return full time to their occupations.'

3. In 1990 pre-clinical French studies reported ozone enhanced the treatment of chemo resistant tumors and seemed to act adjunctively to chemotherapy in tumors derived from the colon and breast.

4. To explore the suspicion that anti-cancer effects of ozone are due in part to its ability to induce release of tumour necrosis factor (TNF), Italian researchers at the University of Siena measured ozonated blood and observed that most TNF was released immediately after ozonation took place. (L Paulesu et al. Lymphokine and Cytokine Res. 1991;10(5):409-12).

5. In 2004 Oxford University reported of a Spanish cancer research institutes human trial of ozone therapy. Involving 19 patients with incurable head and neck tumors receiving radiotherapy and tegafur, plus either chemotherapy (12 patients) or ozone therapy (7 patients). Those receiving ozone intravenously during radiotherapy where on average 10 years older and their tumors significantly more abundant and progressed than the chemotherapy group. But on average the ozone group survived slightly longer than those receiving chemotherapy. They conclude these results warrant further researcher of ozone as a treatment for cancer.

6. Human trials at the Department of Oncology, Nizhni Novgorod State Medical in Russia report benefits of complimentary ozone treatment and with regards to drug complications. Female researchers at the same institute also report “We have followed up on 52 women with breast cancer, 32 patients along with cytostatic therapy have undergone a course of ozone therapy. 20 women were on only conventional polychemotherapy. The groups were compatible according to age, stage of the disease and accompanying pathology. Involvement of ozone therapy diminished the incidence and degree of cytostatics toxical side effects, improve their life quality and immunological parameters and significally increase the activity of antioxidant defence system”.

7. February 28 2008 Marburg Germany - Researchers at the Phillips University Marburg and the University Hospital Giessen and Marburg Germany applied ozone-oxygen peritoneal insufflation to the treatment of rabbit squamous cell carcinomas. This therapy resulted in complete remission of the cancers. Ozone administration has long been known to inhibit the growth of various carcinoma cells in vitro. This study demonstrates ozone’s effectiveness and safety in an in vivo animal model. The study’s data suggests that ”the intraperitoneal application of a medical O3/O gas mixture appears to stimulate the body’s own anti-tumorous immuno-surveillance.” Gerard Sunnen M.D. president of Ozonics International LLC states “If indeed as shown in previous studies internal ozone administration bolsters immune system parameters such as cytokine and NK cell activation this could imply new treatment considerations not only for cancers but also for infectious diseases.”




Peer Studies:

Dr. Sweet, et al., published in Science, a peer reviewed scientific journal - his study showing “Ozone Selectively Inhibits Human Cancer Cell Growth.”



4. 1980 Aug 22nd Sweet F, Kao M S, Lee S-CD (Dept of obstetrics and Gynaecology, WA Univ. School of Medicine, St Louis, Mo) and W. Hagar (St Louis Air Pollution Control) publish in, Science Vol. 209: 931-933, USA peer reviewed scientific journal, their study: O3 Selectively Inhibits Human Cancer Cell Growth.

1991 Oct 1, The peer reviewed JOURNAL OF HAEMATOLOGY published the ozone\HIV work of M.D. Wells, Latino, Galvachin, and Poiesz. Their article: Inactivation Of HIV Type 1 by O3 In Vitro appears in Blood Journal, Volume 78 Number 7, Oct 11, 1991, pg. 1882 describing the research coordinated by Dr. Bernard Poiesz from Syracuse St. Univ. of NY Research Hospital.

They performed 15 replications of one study that interfaced it with HIV infected factor 8 blood. It completely removed the HIV virus 97 to 100 percent of the time, yet was non-toxic to normal blood components. Ed McCabe announced this study back in 1988, in his Oxygen Therapy book.




Peer Reviews:

Wright DT. Ozone stimulates release of platelet activating factor and activates phospholipases in guinea pig tracheal epithelial cells in primary culture. Toxicology and applied Pharmacology 1994;127: 27-36.
Victorin K. Review of genotoxicity of ozone. Mutation Research 1992; 277: 221-238.
McBride DE, Koenig JQ, Luchtel DL, Williams PV, Henderson WR. Inflammatory effects of ozone in the upper airways of subjects with asthma. Am J Respir Crit Care Med 1994; 149:1192-1197.
Morton L. Use of human lung tissue for studies of structural changes associated with chronic ozone exposure: Opportunities and critical issues. Environ Health Persp Supp 1993; (102)Supp.4: 208-213.
Madden MC, Eling TE, Dailey LA, Friedman M. The effect of ozone exposure on rat alveolar macrophage arachidonic acid metabolism. Exp Lung Res 1991;17:47-63.
Doelman CJ. Reactive oxygen species and airway. Amsterdam: Febodruk Ed. 1991:7.
Boorman GA. Ozone and ozone-4 (N-nitrosomethylamino-1-3(3-pyridyl)-1-butanone in Fisher-344/N rats. Tox and Pathol 1994;(22)5: 545-553.
Cajigas A, Mitchell G, Beam C, Steinberg JJ. Ozonation of DNA forms adducts: A 32P-DNA labeling and Thin-Layer Chromatography technique to measure DNA environmental biomarkers. Arch of Environ Health 1994; (49)1: 25-36.
Schulz S. Anticarcinogenic effect of inhaled ozone/oxygen in urethan-treated NMRI-mice. Proceedings Ninth Ozone World Congress, New York 1989: 69-76.
Plopper CG, Duan X, Buckpitt AR, Pinkerton KE. Dose-dependent tolerance to ozone. IV. Site-specific elevation in antioxidant enzymes in the lung of rats exposed for 90 days or 20 months. Toxicol Appl Pharmacol 1994;127: 124-131.
Duan X, Buckpitt AR, Plopper CG. Variation in antioxidant enzyme activities in anatomic subcompartments within rat and rhesus monkey lung. Toxicol Appl Pharmacol 1993;123: 73-82.
van der Wal WA, van Bree L, Marra L, Rombout PJ. Attenuation of acute lung injury by ozone inhalation. The effect of low level pre-exposure. Toxicol Lett 1994; (72)1-3: 291-298.
Muñoz A. Design and analysis of studies of the health effects of ozone. Environ Health Persp Supp 1993; (101)Supp.4: 231-235.
Rilling SH. The basic clinic applications of ozone therapy. OzoNachrichten 1985; Heft 1/2: 7-17.
Viebahn R. The use of ozone in Medicine. 2nd. Rev. Germany: Haugh Pub Ed., 1994: 7, 22, 100.
Rilling SH. 30 years of ozone-oxygen therapy: A historical perspective. Proceedings Eleventh Ozone World Congress. Ozone in Medicine. San Francisco 1993: M-1-3 to M-1-6.
Bocci V. Ozone therapy today. Proceedings 12th World Congress of the International Ozone Association. Ozone in Medicine. Lille, France 1995: 13-27.
Gabrielson EW, Yu XY, SpannhakeWE. Comparison of the toxic effects of hydrogen peroxide and ozone on cultured human bronchial epithelial cells. Env Health Persp 1994; (102)11: 972-974.
Pryor WA, Uppu RM. A kinetic model for the competitive reactions of ozone with amino acid residues in proteins in reverse micelles. The J of Biolog Chem 1993; (268) 5: 3120-3126.
Viebahn, R.: The biochemical process underlying ozone therapy. OzoNachrichten 1985; Heft 1/2: 18-22.
Bocci V. Ozonization of blood for the therapy of viral diseases and immunodeficiencies. A hypothesis. Medical Hypotheses 1992;39: 30-34.
Bocci V. Autohemotherapy after treatment of blood with ozone. A reappraisal. The J of Intern Med Res 1994; 22:131-144.
Bocci V. A reasonable approach for the treatment of HIV infection in the early phase with ozonetherapy (autohemotherapy). How "inflammatory" cytokines may have a therapeutic role. Mediators of inflammation 1994;3: 315-321.
Carpendale MT, Griffiss J. Is there a role for medical ozone in the treatment of HIV and associated infections? Proceedings Ozone in Medicine. Eleventh Ozone World Congress. San Francisco 1993: m-1-32 to m-1-45.
Menéndez S, Iglesias O, Bidot C, Puga A, Carballo A. Application of ozone therapy in children with humoral immunity deficiency. Proccedings 12th World Congress of the International Ozone Association. Ozone in Medicine. Lille, France1995: 271-274.
Basabe E, Menéndez S, Segarra F, Ponce de León M. Ozone therapy like a favoring element in the rehabilitation of children with hearing loss. Proccedings 12th World Congress of the International Ozone Association. Ozone in Medicine. Lille, France, 1995: 275-278.
Jacobs MT. Zwischenfalle und typische komplikationen in der Ozon-saverstoff-therapie. Atti Congresso sull'ozono. Baden-Baden 1981; (11)20: 5-6.
Díaz S, Menéndez S, Eng L, Fernández I. No increase in sister chromatid exchanges and micronuclei frequencies in human lymphocytes exposed to ozone in vitro. Proceedings 12th World Congress of the International Ozone Association. Ozone in Medicine. Lille, France 1995: 43-51.





Medical Books for people who want to learn something valuable in life:


Oxygen Healing Therapies : For Optimum Health & Vitality Bio-Oxidative Therapies for Treating Immune Disorders : Candida, Cancer, Heart, Skin, Circul by Nathaniel Altman, Charles H. Farr

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Oxygen Therapies : A New Way of Approaching Disease (Energy Publications Alternatives , No Oti) by Ed McCabe, Betsy Bullard (Illustrator)

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Hydrogen Peroxide : Medical Miracle by William Campbell, M.D. Douglass, William E. Campbell
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The Use of Ozone in Medicine by Dr. S. Rilling, MD, and R.Viebahn, PhD.
The Use of Ozone in Medicine : A Practical Handbook by Renate Viebahn
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Oxygen Healing Therapies: For Optimum Health and Vitality by Nathaniel Altman



What Is Ozone Therapy?
(Written For The Hartford CT AIDS Project) By Ed McCabe ,
Author of The classic bestseller "Oxygen Therapies" And the new hit "O3 vs. AIDS "

All Rights Reserved and Copyright 2000 by Ed McCabe

PLEASE ONLY WORK WITH COMPETENTLY TRAINED HEALTHCARE PROFESSIONALS WHO ARE REAL OZONE SPECIALISTS SKILLED IN THE OXIDATIVE MODALITIES.

IN AMERICA, OZONE THERAPY IS ONLY TAUGHT PRIVATELY, OR IN NATUROPATHIC SCHOOLS, SO YOUR DOCTOR MAY BE UNTRAINED. THEREFORE, HE WON'T HAVE ANY IDEA WHAT YOU'RE TALKING ABOUT WHEN YOU ASK ABOUT OZONE, AND MAY REACT LESS THAN POSITIVE. SO IF YOU ARE SEEKING OPINIONS, ALWAYS ASK YOUR PROFESSIONAL WHAT REAL WORLD ACTUAL EXPERIENCE HE HAS WITH THE THERAPIES, ESPECIALLY IF HE GIVES A NEGATIVE OPINION. A NEGATIVE OPINION WITHOUT FACTS TO BACK IT UP DOES YOU A REAL DISSERVICE. OVER 7,000 MD's IN EUROPE ARE USING OZONE THERAPY AS YOU READ THIS, BUT NORTH AMERICAN DOCTORS REMAIN WOEFULLY UNINFORMED.

- Ed McCabe

What is 'Ozone Therapy' ?

It's so simple it befuddles the great minds. Unlike healthy human cells that love oxygen, the disease causing viruses, bacteria, fungi, and parasites - including HIV & cancer virons, arthritis microbes, and others - like most primitive lower life forms, are almost all anaerobic .

That means these microbes cannot live in oxygen. Therefore, what would happen to these anaerobic viruses and bacteria if they were to be completely surrounded with a very energetic form of pure oxygen for a long time ? What if enough of this special form of oxygen/ozone was to be slowly and harmlessly introduced into the body daily, over the course of a few months, by bypassing the lungs, and yet eventually saturating all the bodily fluids and every cell with it? Wouldn’t the disease causing microbes that can't live in oxygen cease to exist?

All 30 or so oxygen therapies, including ozone, work because they flood the body with Nature's single oxygen atoms. Singlet oxygen and its by-products are very energetic oxidizers - they "burn up" waste products, pollution, and microbes. They can’t protect themselves because they are either inert, or lower life forms.

Normal body cells protect themselves from the oxidizing effects of oxygen by naturally producing their own protective antioxidant coatings.

We are 66% water. Most European and many American cities purify their municipal drinking water by bubbling ozone through it to kill all the bacteria and viruses, etc. See Inactivation Kinetics of Viruses and Bacteria by use of Ozone, by E. Katzenelson, et. al., American Water Works Society, 1974 .

Most bottled water in the U.S. goes through the same ozone purification methods. Since your body is two-thirds water (we are internally permeated with fluids), the same purification principals would directly apply to us. Ozone is simply infused through your personal body liquids to sterilize and purify them.

This method has been successfully applied to the human body by knowledgeable doctors treating diseased persons for over 100 years. It's simple. Our natural intake of oxygen from food, air, & water is the way Nature intended us to keep healthy and clean by naturally oxidizing away the microbes and toxins. Unfortunately, due to human ego and greed, mankind has polluted the eco-system, cut down the rainforests, and ruined the oceans, the two sources of where the oxygen all comes from. So because we are all oxygen deficient, our bodies can no longer take out (oxidize) the trash. Even the ozone layer above us that protects us from ultraviolet rays is born when the rainforests make the oxygen that eventually turns into ozone. The removal of our planet's oxygen generating forests, and atomic bomb testing rendering the natural oxygen isotopic and unable to turn into ozone, is directly relating to the "mysterious" holes in the ozone layer.

I have witnessed hundreds of AIDS and other patients receiving ozone infusion therapy. When they start out their blood is filthy, diseased, and so empty of oxygen that it is almost black in color from the filth. Keep putting the ozone into them for a while, and the blood turns back to a bright cherry red color, full of life giving oxygen and clean . Human ego is presently preventing us from exploring ozone's use in US medicine without great difficulty. For example, In New York City it is illegal to say any therapy helps AIDS. This law has been used as an excuse to shut down experimental ozone clinical trials in progress before they could produce the documentation. There is plenty of documentation already around in major journals.
See Ed McCabe's "O3 vs. AIDS " for hundreds of medical references.

50+ years of Ozone application methods

Extracorporeal recirculatory autohemo perfusion . Blood out of one arm, ozonated, sterilized and filtered outside the body, and pumped continuously back into the other arm. The best.

IV slow injections of the O3 gas - no air, just pure medical grade oxygen turned into medical grade ozone – into prone patients. 27 mcg/ml3 concentration. Air bubbles? No nitrogen, no nitrogen (air) embolisms.

Autohemotherapy - withdrawing 600 ml of blood and re-infusiing it into the body after putting ozone into it.

Ozone bagging - every body part except the head in a bag full of O3 for up to two hours.

Ozone rectal insufflation - average 1 1/2 liters of 27mcg/ml O3 gas into colon.

Ozone vaginal insufflation - average 5 minutes of insufflating body cavity.

Ozone ear insufflation - average 5 minutes of letting O3 fall into ear cavities.

Ozone air purification - low levels of ozone sterilize and rejuvenate the room air. O3 in LOW doses cleans the lungs and blood.

Ozone charged drinking water – Bubble O3 into water which must be imbibed immediately while the O3 is still in the glass. There are over 3,000 medical references in the German literature showing ozone's use in over 50 years of application to humans by way of millions of dosages. The International Ozone Association and the ozone machine manufacturers report over 7,000 M.D.'s in Europe using medical ozone safely and effectively, some for more than 40 years, yet for the past 15 years, the FDA has prevented formal human testing or any ozone generating device approvals.

I have seen people sero-convert to HIV PCR negative, and even more importantly, lose all secondary infections from being on ozone. BUT they stuck to a full protocol - getting it daily, IV, the right dosage, and the right concentrations, and combining it with other significant modalities. People who have never tried it, or only just "dabbled" in it, end up being the only nay sayers. Go ahead and ask anyone who is disrespecting ozone - Ask them, did you work up to using at least 150cc (not the starting dosage) of 27-42 mcg/ml concentration strength of only pure medical ozone gas? Was it once or twice a day, every single day, for four to six weeks? Was the ozone delivered IV or better? If they say it's dangerous, or ineffective, they're doing it wrong! 99% of the many successful people that I have interviewed - and written or spoken about - have received ozone only this proper way. And none were hurt. - see below on the 5 1/2 million dosage German study showing ozone to be completely safe. Those that use ozone continue to come back for more because they live the benefits within their own bodies. The German Medical Society has published that 384,775 patients were treated with ozone with a minimum of 5,579,238 applications and the side effect rate observed was only .000005 per application! No medicine has anywhere near this low of a side effect rate! Outrageously safe when applied correctly. The report also stated "The majority of adverse effects were caused by ignorance about ozone therapy (operator error)." The University of Innsbruck's Forensic Institute published Dr. Zacob's dissertation quoting this in The Empirical Medical Acts of Germany.

 

[nbhadja]

BUMP BUMP BUMP- The FDA has done everything in its power to help the pharmecutical companies and suppress Ozone therapy. Most people in America do not even know what it is.

http://www.familyhealthnews.com/articles-ask-mr-oxygen-ed-mccabe.html

"For example, In New York City it is illegal to say any therapy helps AIDS.

This law has been used as an excuse to shut down experimental ozone clinical trials in progress before they could produce the documentation. There is plenty of documentation already around in major journals. See Ed McCabe's "O3 vs. AIDS" for proof. "

"Ozone therapy was accepted medicine in the USA from at least 1880 until 1932, a period of fifty-two years. "

"In 1929, a book called "Ozone and Its Therapeutic Action" was published in the USA. It listed 114 diseases and how to treat them with ozone. Its authors were the heads of leading American hospitals."

" In 1933, the American Medical Association (AMA), headed up by M. Fishbein, set out to eliminate in the USA all medical treatments that were competitive to drug therapy. The suppression of the use of ozone therapy by doctors in the USA began then, and continues to this day, except in thirteen states, where currently doctors are protected by state laws.

[See below for a list of the 13 states]

At the behest of the AMA, the FDA began seizing ozone generators in the 1940s.

So now you know, very briefly, the generally unknown history of ozone therapy in the USA.

Since 1933, the AMA and the FDA have done everything in their power to prevent ozone therapy from being used or even known about, in order to protect the profits of the pharmaceutical industry and promote the practices of the membership of the AMA.

These days, the FDA and the giant pharmaceuticals have interlocking directorships. (People are working, and taking money, from both sides, while still supposedly maintaining their impartiality - Dennis)"

 

[dannno]

That's probably because the virus is 'inactive' to begin with.

 

[nbhadja]

That's probably because the virus is 'inactive' to begin with.

No, it is active. If it was inactive it would not be a problem.

The FDA is a terrorist organization for the way they eliminated all knowledge about Ozone therapy in the US and ban it from being practiced.

Those morons release anti cancer drugs that are so toxic that it kills many people, yet they harp about the ozone therapy not having enough research on it (which is pure BS as it is used a lot in Europe).

 

[dannno]

No, it is active. If it was inactive it would not be a problem.

The FDA is a terrorist organization for the way they eliminated all knowledge about Ozone therapy in the US and ban it from being practiced.

Those morons release anti cancer drugs that are so toxic that it kills many people

You should look into AZT, because Dr. Duesberg of the University of California at Berkeley believes that is what was killing many of the early patients diagnosed with HIV. The newer drugs are less toxic, therefore patients with HIV are now living longer. People who don't understand what is happening will point to studies that show the drugs are getting better which only furthers my point, and you cannot point to any studies that would give true integrity to the position that HIV actually causes AIDS. Dr. Duesberg does not believe that HIV causes AIDS, and he has specialized in retro-viruses his entire life. Many other conditions can cause AIDS, including drug use, malnutrition and a specific disease that occasionally is seen and is a result of anal sex and is completely treatable. There are a lot of people who have HIV and never know it and lead completely normal lives in good health. In fact the virus has been around for a long time and there are probably a lot of old people who have had HIV since the early part of the last century. The occurrences of HIV since they have begun testing for it have increased with the increase in testing. There's much more to the subject. It is outlined pretty well in the film Deconstructing the Myth of AIDS as well as Peter Duesberg's books.

http://www.youtube.com/watch?v=FoxCtYBXNpc

 

[idiom]

How would Ozone Therapy 'cure' a retro-virus? It can contain its effects, but living with a continuous ozone drip for the rest of your life would be deleterious.

Sounds like it might be a fun alternate to irradiating your self when dealing with cancer though.

 

[zach]

Despite the importance of the results which would indicate that simple ozonation of the blood supply would render it free of HIV, as well as herpes, hepatitis and other viruses the Canadian findings received little notice in the North American press.

We're never told anything that's good for us.

 

[nbhadja]

How would Ozone Therapy 'cure' a retro-virus? It can contain its effects, but living with a continuous ozone drip for the rest of your life would be deleterious.

Sounds like it might be a fun alternate to irradiating your self when dealing with cancer though.

Actually it works extremely well and it has only benefits. It is widely used outside of the US.

It shuts down the virus , cancer cells etc because the blood becomes so oxygen rich those cells hate it.

 

[Magicman]

http://www.scribd.com/doc/8788977/Ozone-Blood-Treatment-Cures-Aids-Victims-in-Germany



Here is a great article everyone. This you can send and is more legible.

 

[Magicman]

Actually it works extremely well and it has only benefits. It is widely used outside of the US.

It shuts down the virus , cancer cells etc because the blood becomes so oxygen rich those cells hate it.

Great video to watch about Ozone Therapy:

http://www.youtube.com/watch?v=4zzBEtR91OQ


I have read articles from German Doctors that are trying hard to put this information to U.S. medical studies and get rejected so their leaking out information. It seems like the U.S. system is so far down the path with pharmaceuticals that the U.S. Medical Board is suppressing this information because it would cut their profit potentials and it's safe and extremely effective.




Oxygen therapy is a form of treatment that uses oxygen to heal various disease conditions and strengthen the immune system. Hyperbaric oxygen therapy (HBO) is a mainstream treatment that involves placing the patient in a pressurized chamber with pure oxygen (O2). Bio-oxidative therapies are alternative treatment approaches that emphasize increasing the oxygen content of the blood through proper breathing and diet, together with the use of ozone and/or hydrogen peroxide in the treatment of specific diseases or weakened immune systems. Ozone therapy is considered a mainstream form of medical treatment in Germany, Austria, Switzerland, France, and Russia.

HBO therapy is used to reverse conditions or processes caused by inadequate oxygen in the body (e. g., asthma, carbon monoxide poisoning, smoke inhalation, decompression sickness, and mountain sickness) or to speed up the healing of injuries or infections by increasing the amount of oxygen in body tissues.

For this type of treatment, the patient is placed in a pressurized chamber and breathes pure oxygen either circulating within the chamber itself or through a mask or tube. Patients being treated for carbon monoxide or smoke inhalation poisoning receive oxygen through a tight-fitting aviator or anesthesia mask. The length of time in the oxygen chamber, the degree of pressurization, and the number of treatments depend on the condition being treated. For example, decompression sickness from diving accidents may require up to two weeks of oxygen treatment. Patients with osteomyelitis may require as many as 40-60treatments. Treatment sessions for most conditions are 90 minutes, with one or two five-minute "air breaks" at 20-minute or half-hour intervals.

Risks associated with hyperbaric oxygen treatment include seizures, irritation of the inner ear, numbness in the fingers, and temporary changes in the lens of the eye. In rare cases, HBO causes inflammation of the optic nerve thatmay lead to blindness.

Bio-oxidative therapies are used to treat conditions ranging from AIDS, cancer, and cardiovascular diseases to acne, dental surgery, allergies, arthritis,and herpes infections. Ozone therapy and hydrogen peroxide therapy are usedto treat a variety of diseases. Ozone and hydrogen peroxide are thought to inhibit tumor growth, kill viruses, stimulate the production of disease-fighting white blood cells, and improve the efficiency of oxygen transfer from the blood to body tissues.

Ozone can be administered in various ways. Mixtures of ozone and oxygen may be injected into muscle or introduced into the rectum. Doctors in Germany and Russia inject ozonated water into patients' joints to treat arthritis, rheumatism, and other joint diseases. Ozonated water is also used to cleanse or disinfect wounds, burns and skin infections and to treat the mouth after dentalsurgery. Ozone-treated oils are used to treat fungal infections, insect bitesand stings, acne, and similar skin problems. Slow-healing wounds are sometimes treated by pumping a mixture of ozone and oxygen into an airtight bag surrounding the area to be treated. The mixture is absorbed into body tissues through the skin. A method called autohemotherapy is used in Cuba to treat HIV infection, herpes, arthritis, and cancer. It involves removing 10-50 mL of a patient's blood, treating it with a mixture of ozone and oxygen, and then reinjecting or reinfusing it into the patient.

Hydrogen peroxide (H2O2) is a colorless liquid that mixes easily with water. Weak solutions of hydrogen peroxide are given intravenously for treatment of pneumonia, or influenza, and certain chronic diseases.Intravenous infusions of hydrogen peroxide also appear to help the immune system by stimulating production of white blood cells. Hydrogen peroxide solutions can also be injected directly into joints and soft-tissue to treat arthritis and other inflammatory conditions.

 

[Magicman]

Ozone Therapy: The Science Behind the Scandal

AIDS NEWS SERVICE
Michael Howe, MSLS, Editor
AIDS Information Center
VA Medical Center, San Francisco
(415) 221-4810 ext 3305
April 15, 1994

OZONE THERAPY (Part I)

Ozone therapy, involving doses of the reactive oxygen gas, has long been in Europe a popular alternative treatment for a variety of ailments. While health authorities chide practitioners for using this "unproven" therapy, reports continue to describe favorable results. Scientists also continue to investigate the potential of ozone therapy to eliminate disease-causing organisms from the bloodstream. In the mid-1980s, German researchers began using a process called autohemotherapy to test the use of ozone on blood infected with HIV and hepatitis B and, in 1986, a biotech company called Medizone International was created to follow up on the approach.

Since then, Canadian and American scientists have confirmed ozone's direct antiviral effects, and its ability to boost key parts of the immune system. Last May, a Canadian study reported that ozone completely inactivated SIV, the simian equivalent of HIV, in monkey blood. The implications for safeguarding the blood supply are clear, although the therapeutic potential is not. Nevertheless, according to Medizone, preliminary trials are being conducted at five centers in Italy using an ozone/oxygen mix to treat patients with HIV and hepatitis B. A great deal of research remains to be performed on ozone, but advocates predict that because ozone cannot be patented, it will not attract financial backing for the scientific studies needed to win FDA approval. Longevity (04/94) Vol. 6, No. 5, P. 54.

Frankum B. Katelaris CH. Ozone Therapy in AIDS--Truly Innocuous? [letter]. Med J Aust. 1993 Oct 4;159(7):493.

Carpendale MT. Freeberg J. Griffiss JM. Does Ozone Alleviate AIDS Diarrhea? J Clin Gastroenterol. 1993 Sep;17(2):142-5.

Five patients with acquired immune deficiency syndrome (AIDS) or AIDS-related complex (ARC) and intractable diarrhea were treated with daily colonic insufflations of medical ozone (oxygen/ozone mixture) for 21-28 days. The daily dose of ozone (O3) ranged from 2.7 to 30 mg. Three of the four patients whose diarrhea was of unknown etiology experienced complete resolution, and one patient had marked improvement. The fifth patient, whose diarrhea was due to Cryptosporidium, experienced no change. No consistent change in the absolute number of helper (CD4) or suppressor (CD8) lymphocytes was detected, and no obvious changes were seen in the PO2 or the results of routine hematologic and blood chemistry studies. Patients had mild to moderate local discomfort during ozone administration early in the course of treatment, but no adverse systemic effects were observed. The results of this series suggest that medical ozone administered by rectal insufflation is simple, safe, and effective. Should this simple treatment be used routinely to treat chronic intractable ARC/AIDS diarrhea?

Carpendale MT. Griffiss J. Is There a Role for Medical Ozone in the Treatment of HIV and Associated Infections? In: Ozone in Medicine. Proceedings of the Eleventh Ozone World Congress, August 29-September 3, 1993, San Francisco, CA. PP. M-1-32-M-1- 45. International Ozone Association, Pan American Committee, 31 Strawberry Hill Ave., Stanford, CT 06902-2608.

Medical Oxone inactivates many pathogenic viruses including HIV in vitro. Pilot studies in man suggest positive benefits in the early stages of HIV infection (t-4 cells greater thanf 400).

These include incrased T4 and T8 cells, normalizing of T4:T8 ratio, and a general feeling of wellbeing and minimal evidence of infection. Improvement also occurs in AIDS patients (T4 cells less than 200) but less evidence of T4 cell resurgence. These studies indicate that at least in vitro there is a good safety margin between the ozone dose required to inactivate HIV and the earliest suggestion of suppression of lymhocytes. In fact, the lymphocytes are being stimulated at doses that completely inactivates HIV. More work needs to be done to clarify the most effective dosage and means of treating HIV infections with medical ozone.

LoLordo, Ann. AIDS Treatment Documentary Premieres Amidst Controversy. PR Newswire, San Francisco, 08/30/93.

The medical world [criticized] a documentary about an unapproved medical treatment called ozone therapy, which may allegedly deter cancer and AIDS. Canadian filmmaker Geoffrey Rogers' "Ozone and the Politics of Medicine" [described] a potential breakthrough drug that is dismissed by health officials, although millions of patients in Europe have already used it. Rogers [included] scientific evidence that ozone can inhibit cancer cells and inactivate viruses. A recent study by the Canadian military and the International Red Cross discovered that monkeys injected with blood plasma tainted with SIV, the primate equivalent of the AIDS virus, died within two weeks. Monkeys receiving ozone injections, however, remained healthy and were not infected. The Food and Drug Administration has condemned ozone therapy, and even labeled its use as health care fraud. The drug gained national attention [in July, 1993] when the famous New York doctor Robert Atkins lost his medical license over a complaint about the use of ozone therapy. Dr. Atkins' license was subsequently reinstated.

Wolfstadter HD. Sacher J. Hopfenmuller W. Stange R. Retrospective Benefit Following Individualized Naturopathic Therapy in HIV-patients at Different Stages. Int Conf AIDS. 1992 Jul 19-24;8(3):147 (abstract no. PuB 7588).

OBJECTIVE: To assess the long-term efficacy and benefit of a complementary treatment regimen, we investigated on laboratory findings and clinical outcome in a cohort of 175 out-patients (CDC II-IV E) successively treated since 1986. METHODS AND PATIENTS: The therapeutic regimen comprised autologous ozone transfusions, homeopathy, phytotherapy, therapy with enzymes, mineral-, vitamin- and trace element substitution, nutritional management, correction of intestinal dysbacteria and psychophysical means, set up on an individualized basis. No conventional antiviral therapy was given. Patients (all male homosexuals) were divided into 5 groups (Gr. I-V) according to their CD4 lymphocyte counts at entry into therapy (Gr.I n = 22, CD4 0-50; Gr. II n = 12, CD4 51-100; Gr. III n = 17, CD4 101- 200; Gr. IV n = 81, CD4 201-500; Gr. V n = 53, CD4 greater than 500 [/microliters]) and 15 hematological and biochemical parameters were evaluated with individual regression analysis according to the length of observation of patients (min. obs.time in Gr. I-III 3 months, min. obs.time in Gr. IV and V 6 months). Moreover we studied the incidence and severity of opportunistic infections and overall QOL during the observed period. RESULTS: Patients in Gr. I presented a median loss of CD4 lymphocytes per month of 0.54 cells/microliters(range -42.0 to 4.50, median obs.time 8 months), Gr. II median loss 3.65 cells/microliters (range -5.9 to 8.8, median obs.time 10.5 mo.), Gr. III median loss 4.98 cells/microliters (range -13.5 to 11.0, median obs.time 16.8 mo.). In Gr. V, apparently due to the earlier stage of disease, no clear statistical trend of helper- cell deterioration could be observed. Patients in Gr. IV, with an approved indication for antiviral therapy, presented a median loss of CD4-cells of 4.47/microliters (range -17.2 to 37.5, median obs.time was 25.4 mo.).

Compared to CD4 lymphocyte deterioration given in the literature for patients under antiviral therapy, 52% of our patients in Gr. IV exceeded these values, while 24.6% remained below. No substantial adverse events or side effects accompanied the therapies, thus we found QOL generally increased. CONCLUSIONS: Our results suggest that patient performance under a combined and individualized naturopathic regimen might be to some extend improved with respect to data collected from cohorts in the literature. Further investigation including controlled clinical trials on different aspects of the single therapies is necessary.

Brown, David. A New Look at Alternative Therapies. Washington Post (Health), 06/23/92, P. 8.

The National Institutes of Health will soon examine alternative therapies more closely because of the possible efficacy of the treatments. John C. Pittman, a physician in Raleigh, N.C., discontinued his ozone gas therapy for AIDS patients after the North Carolina Board of Medical Examiners told him they were looking into his controversial practices. However, an advisory board at the NIH last week expressed interest in Pittman's work and requested more information on his claim that three out of 25 patients with HIV had overcome the virus after having the highly reactive gas inserted into their blood. Ed McCabe, author of a book on unconventional uses of oxygen, also told an NIH panel how ozone treatment had significantly improved the conditions of 300 HIV-positive patients. In ozone therapy, a blood sample can be treated with the gas and returned to the patient, or a small volume of gas can be inserted directly into the vein. Advocates say the procedure should be done twice daily for three weeks to treat HIV infection. The Office for the Study of Unconventional Medical Practices, established after the 1992 federal budget requested that NIH spend at least $2 million on such an effort, will attempt to determine which treatments may be promising and can be tested in conventional experiments.

Hooker MH. Gazzard BG. Ozone-Treated Blood in the Treatment of HIV Infection [letter; comment]. AIDS. 1992 Jan;6(1):131.

Carpendale MT. Freeberg JK. Ozone Inactivates HIV at Noncytotoxic Concentrations. Antiviral Res. 1991 Oct;16(3):281- 92.

The inactivation of human immunodeficiency virus (HIV) and cytotoxic properties of ozone-treated serum and serum- supplemented media were examined. The titer of HIV suspensions in human serum was reduced in a dose-dependent manner when treated with total reacted ozone concentrations at a range of 0.5 to 3.5 micrograms/ml-1. Complete inactivation of HIV suspensions was achieved by 4.0 micrograms/ml-1 of ozone in the presence or absence of H-9 cells. In contrast, cellular metabolism, as measured by MTT dye cleavage, and DNA replication, as measured by BUdR incorporation, were enhanced in H-9 cells grown in media treated with quantities of ozone that completely inactivate HIV. The permissively HIV-infected cell line HXB/H-9 was cultured in ozone-treated media for six days with culture supernatants being sampled and assayed on alternate days for HIV p24 core protein. HIV p24 was reduced in all treated cultures compared to control cultures, with an average reduction of 46% [p24].

Wells KH. Latino J. Gavalchin J. Poiesz BJ. Inactivation of Human Immunodeficiency Virus Type 1 by Ozone in vitro. Blood. 1991 Oct 1;78(7):1882-90.

A device was designed to deliver a constant source of given concentrations of ozone to fluids containing human immunodeficiency virus type 1 (HIV-1). Ozone was found to inactivate HIV-1 virions in a dose-dependent manner. Greater than 11 log inactivation was achieved within 2 hours at a concentration of 1,200 ppm ozone. Similar concentrations of ozone had minimal effect on factor VIII activity in both plasma and immunoaffinity-purified preparations of factor VIII treated for the same time period. The data indicate that the antiviral effects of ozone include viral particle disruption, reverse transcriptase inactivation, and/or a perturbation of the ability of the virus to bind to its receptor on target cells. Ozone treatment offers promise as a means to inactivate human retroviruses in human body fluids and blood product preparations.

Garber GE. Cameron DW. Hawley-Foss N. Greenway D. Shannon ME. The Use of Ozone-Treated Blood in the Therapy of HIV I=fection and Immune Disease: A Pilot Study of Safety and Efficacy [see comments]. AIDS. 1991 Aug;5(8):981-4.

The use of ozone therapy is reported to be effective in a variety of viral illnesses, including HIV disease. We performed a phase I study of ozone blood treatments in 10 patients in whom no significant toxicity was observed. Three patients with moderate immunodeficiency showed improvement in surrogate markers of HIV-associated immune disease. A phase II controlled and randomized double-blinded study was initiated comparing reinjection of ozone-treated blood, and reinjection of unprocessed blood for 8 weeks, followed by a 4-week observation period. Ozone had no significant effect on hematologic, biochemical or clinical toxicity when compared with placebo. CD4 cell count, interleukin-2, gamma- interferon, beta 2- microglobulin, neopterin and p24 antigen were also unaffected by both treatment arms. In conclusion, ozone therapy does not enhance parameters of immune activation nor does it diminish measureable p24 antigen in HIV-infected individuals.

Mayer C. Soyka. Naber D. [Paranoid hallucinatory psychoses in an HIV infected patient on ozone therapy]. Nervenarzt. 1991 Mar;62(3):194-7.

Roder W. Muller WE. Merz H. [Is Ozone Suitable for Sterilization of HIV infected Bones?] Unfallchirurg. 1991 Jan;94(1):50-1.

HIV infection can be transferred by blood, blood products and organ transplantation. In traumatic surgery allogeneic bone transplantation is commonly used for reconstruction in severe bone injuries. This technique has been abandoned since the appearance of reports of infections with HIV. In an experimental in vitro study we showed that ozone treatment cannot inactivate HIV in bone for transplantation.

Wagner K. Mayers D. Toro L. Baker JR Jr. The Effect of Ozone (03) on Lymphocyte Populations in Normal and HIV1-Infected Blood. Int Conf AIDS. 1989 Jun 4-9;5:656 (abstract no. C.587).

OBJECTIVE: Measure the effect of varying 03 concentrations on lymphocytes in whole blood from an uninfected and a Walter Reed Stage 2 HIV1 patient. METHODS: Heparinized whole blood samples were exposed in triplicate to (03) of 20, 40, and 60 ug/ml with an oxygen control. Coded, blinded blood samples were gently agitated for 10 min. and incubated for 1 hr. at 27 C. Mononuclear cells were separated using Ficoll-hypaque gradients and stained for FACS analysis using labelled monoclonal antibodies. RESULTS: 03 had no effect on lymphocyte populations of the uninfected donor as numbers of total T cells, CD4, CD8, and B cell subpopulations did not change. In contrast, there were marked changes in the lymphocyte populations of the HIV positive donor with increasing (03). CONCLUSIONS: Ozone, at concentrations previously shown to inactivate HIV1, may alter lymphocyte surface markers in HIV1 infected patients. Further studies are indicated to examine this effect.

****************************************************************

[Editor's Note: This is the text of a letter from Medizone International Inc. in response to inquiries regarding ozone.]


Medizone International Inc
123 East 54th Street,
Suite 2H,
New York
NY 10022
(212) 421-0303
Fax: (212) 888-2798

June 29, 1993

Dear xxxx,

Thank you for your letter. At present Medizone International Inc and Medizone Canada Ltd are awaiting US Food and Drug Administration and Canadian Health and Welfare approval, respectively, to commence human clinical trials for the use of the Medizone (R) (ozone/oxygen) drug in the treatment of Acquired Immune Deficiency Syndrome (AIDS). The following is a brief overview of Medizone International Inc's research to date.

Acquired Immune Deficiency Syndrome (AIDS) is a condition described in 1981 and found to be caused by a retrovirus (HILV- III/HIV). To date, treatment only affords temporary suppression of the virus.

Since the identification of Acquired Immune Deficiency Syndrome (AIDS), researchers have employed many modalities to treat patients with HIV-related disease. In Europe, one modality employed has been an ozone/oxygen mixture. The mixture is introduced into fixed volumes of the patient's blood 'ex vivo'. This procedure has been entitled autohemotherapy, but may be referred to more descriptively as extracorporeal circulation. Anecdotal reports on the results of this work are extremely encouraging. However, in view of the fact that no controlled trials have been performed, these results must be carefully evaluated.

In March 1986 Medizone International Inc was created specifically to scientifically evaluate this treatment and bring the technology to market. A series of studies were undertaken to establish:

a) the safety of extracoporeal circulation with an ozone/oxygen (Medizone(R)) mixture in a variety of animal models (toxicity studies);

b) the effect(s) of ozone/oxygen mixture (Medizone(R)) on a human HIV target cell line, HUT-78;

c) the anti-retroviral activity of ozone/oxygen (Medizone(R)) on HIV 'in vitro';

d) the effect of ozone/oxygen (Medizone(R)) in human peripheral blood 'ex vivo';

e) the effect of ozone/oxygen (Medizone(R)) on exogenously HIV-1 'spiked' Factor VIII preparations.

The studies and results to date include:

a) A preliminary rabbit animal model treated with (ozone/oxygen) Medizone(R) in a manner analogous to the proposed human treatment regime at the Long Island College of Pharmacy suggested no toxicity at concentrations up to ten times the dose proposed in man.

b) A limited feline model toxicity study performed at the Cornell Feline Health Centre, Cornell Veterinarian College, Ithaca, to investigate the relative toxicity of Medizone(R) has yielded no detectable toxic effects.

c) Cell-free HIV treated with (ozone/oxygen) Medizone(R) resulted in 100% inactivation of the virus while maintaining HUT-78 viability. These studies were performed at the State University of New York at Syracuse under the auspices of Dr Bernard Poiesz.

d) Implementation of a patented hollow fibre technology has demonstrated Medizone(R)'s ability to *reduce* intracellular viral expression by greater than 99% while maintaining target cell viability.

e) Treatment of human peripheral blood with Medizone(R) revealed hemolysis and coagulation changes well within the standard for re-infusion of packed human blood. These studies were performed at the Mount Sinai School of Medicine in New York, under the auspices of Dr Michael Greenburg.

f) Published results (Blood, Vol. 78(7):1882, 1991) involving the treatment by Medizone(R) of Factor VIII preparations exogenously 'spiked' with HIV-1 yielded a minimum (ten) log diminution of viral load while maintaining 90% biological activity of this blood component.

g) Investigation with Visna Virus and Feline Intestinal Peritonitis Virus, two lipid enveloped viruses, have been inactivated with measurable lipid peroxides derived from Medizone(R) treatment.

h) 'In vitro' inactivation by Medizone(R) of a variety of Simian Immune Deficiency (SIV) variants studied through a multi-agency Canadian government collaboration have paralleled those results published by Poiesz et al.

The hypotheses underlying ozone's virucidal activity are based upon the drug's propensity toward lipid peroxidation. Those viruses which are lipid-encapsulated (ie. lentivirus family) are highly susceptible to the direct oxidative effect of ozone, and are thereby inactivated.

Data indicate the differential effect on lipid envelope viruses versus those whose lipid capsid composition is minimal.

We postulate that ozone will inactivate cell-incorporated viruses by at least two discreet mechanisms:

1. Due to the high degree of lipid peroxidation catalysed by ozone interaction(s), viral binding to specific receptors (ie. HIV to CD4A receptor), whose membranous nature (both viral coat and receptor) implies a finite composition of lipid [including polyunsaturated fatty acids (PUFA)], may indeed be ozone sensitive. Investigations with Rhodamine-labelled HIV, challenged with ozone sensitized HIV virions, have suggested alterations in receptor/ligand binding capacity yielding diminished viral binding. This data suggests that ozone, delivered by hollow fiber technology at antiviral concentrations, does impair HIV's ability to bind to CA4A + target cells.

2. It has been demonstrated that target cells with pro-viral DNA incorporated into its genome have decreased titers of certain protective enzyme systems with respect to oxidative perturbations. In particular, superoxide distumase (SOD), catalase (CAT) and glutathione peroxidase (GSHPx) levels are diminished in a number of virally transformed cell lines. Such decreases may render these cells selectively sensitive to the oxidative effects initiated by ozone. It should be noted that ozone's effects are instantaneous with regard to peroxidation and the products of this reaction with cellular membrane lipids (hydroperoxides) are relatively stable and can participate in a host of oxidative (including free-radical) propagating reactions. It is our intention to generate, via ozone's direct activity and product(s) derived through lipid interactions, data to support:

a) inactivation of those viruses [ie. HIV, Hepatitis B, non-A and non-B (Hepatitis C)] associated with transfusion associated diseases while maintaining the replacement value of the blood fractionate of interest (ie. plasma proteins, packed red cell preparations and platelets).

b) reduction of cell incorporation by virus through impairment of viral-receptor binding;

c) inactivation of cell-incorporated virus render them non- viable while maintaining normal target cell viability.

The results of experimental work have demonstrated non-toxicity in treating; a preliminary animal rabbit model, human HIV target cells, a limited feline model, human peripheral blood, and Factor VIII preparations exogenously 'spiked' with HIV-1, all with ozone/oxygen mixtures (Medizone(R)). Anti-retroviral was demonstrated at concentrations maintaining HUT-78 viability, as well as Factor VIII biological activity, respectively.

On June 2nd, 1993, Medizone International Inc announced the successful completion of the first two phases of a Canadian research project that has demonstrated preliminary scientific evidence supporting the use of the company's blood decontamination technology in a live, primate (monkey) model.

In making the announcement, Medizone president, Dr Joseph S Latino said, "To date, the research program has successfully demonstrated that monkeys receiving blood fractioned plasma, purposely infected with a highly virulent strain of Simian Immunodeficiency virus (monkey equivalent to HIV), but treated with Medizone's process, did not demonstrate any signs of infection over the course of the study (35 days). However, all animals receiving similarly infected products without the intervention of Medizone's contamination technology died within 12-14 days."

This research project was under the direction of an international collaborative team of scientists representing the Canadian Red Cross, Canadian Departments of Defence and Agriculture, Cornell University Veterinary Medical College, and Medizone Canada Ltd.

Please do not hesitate to contact me should you require any additional information.

Your sincerely,

Katherine M Kalinowski
Corporate Secretary

 

[RonPaulVolunteer]

Thanks for this...

 

[nbhadja]

bump

 

[Bossobass]

I've known about Ozone (and food grade peroxide) for years. Also look at anti-angeogenesis drugs and feverfew (parthenolide) for killing cancers of all sorts, as well as curing migraines, macro-degeneration, leprosy, inflammatory bowel disease and other maladies.

They'll remain in "clinical trials" for eternity, or just be outlawed. Clinical trials are just rigged-to-fail charades. You have to be clinically dead to qualify.

My father's been dead almost nine years now, and they have yet to begin the anti-angiogenesis trials they had him sign up for in 2000, which were only to be conducted in tandem with chemotherapy drugs.

In this country, it's every man for himself.

Thanks for posting the info. It's a great subject that gets zero press.

Bosso

 

[DAFTEK]

I got some reading to do....10x

 

[Ninja Homer]

Another up-and-coming alternative cure for cancer and AIDS (and many other diseases) is MMS. It's very cheap and easy to take. It's also wonderful for detox.

This is a must-read if MMS is new to you: http://phaelosopher.wordpress.com/2007/09/09/no-miracle-just-wonderful-chemistry/

More info:
http://www.understanding-mms.com
http://www.miraclemineral.org/
http://mms-articles.com/
http://curezone.com/forums/f.asp?f=871

 

[BlackTerrel]

No, it is active. If it was inactive it would not be a problem.

The FDA is a terrorist organization for the way they eliminated all knowledge about Ozone therapy in the US and ban it from being practiced.

Those morons release anti cancer drugs that are so toxic that it kills many people, yet they harp about the ozone therapy not having enough research on it (which is pure BS as it is used a lot in Europe).

Could you compare cancer rates and deaths between Europe and the US. If what you say is true there should be a large difference between the populations.

Edit: This was the first good link I found. Says cancer treatment is better in the US than in Europe.

http://www.medscape.com/viewarticle/561737

August 22, 2007 — New reports from EUROCARE suggest that cancer care in Europe is improving and that the gaps between countries are narrowing. However, comparisons with US statistics suggest that cancer survival in Europe is still lagging behind the United States. The reports are published online August 21 in Lancet Oncology and scheduled for the September issue....

...One of the reports compares the statistics from Europe with those from the United States and shows that for most solid tumors, survival rates were significantly higher in US patients than in European patients. This analysis, headed by Arduino Verdecchia, PhD, from the National Center for Epidemiology, Health Surveillance, and Promotion, in Rome, Italy, was based on the most recent data available. It involved about 6.7 million patients from 21 countries, who were diagnosed with cancer between 2000 and 2002.

 

[Magicman]

Another up-and-coming alternative cure for cancer and AIDS (and many other diseases) is MMS. It's very cheap and easy to take. It's also wonderful for detox.

This is a must-read if MMS is new to you: http://phaelosopher.wordpress.com/2007/09/09/no-miracle-just-wonderful-chemistry/

More info:
http://www.understanding-mms.com
http://www.miraclemineral.org/
http://mms-articles.com/
http://curezone.com/forums/f.asp?f=871

Yes, I heard that was awesome. That guy is pretty amazing to cure 65,000 people of Malaria. What's interesting is so many of these methods all lead to oxidative-based methods. I've heard many good things about it. So many celebrities are talking about therapies like Hyperbaric Oxygen Chamber. Remember Pamela Anderson had herpes. Dave Navarro and Michael Jackson use it too. If it wasn't effective why would they be going that route for these types of viruses or for its anti-aging properties? That is a very powerful oxidative treatment that it seems like the general public isn't too informed about.

What makes MMS and Ozone Therapy special is the affordability factor hence why it's so suppressed.

It seems there banning colloidal silver and suppressing Ozone treatment in favor of maximixing pharmaceutical potential. To me, it seems like genuinely these people have a lot more to lose and the pharmaceutical industry to gain so why are they always put on sites like Quackerywatch. A complete disinfo site which goes after these methods.

This guy I cannot back his claims just yet but his name is Dr. Bob Beck, and he developed his own protocol and passed away. I think he's in the right direction because if Ozone has made those claims, and I've heard stories about Tetrasil (a special patent of Colloidal Silver) curing people in Zambia then he's taken this a huge step further by electrifying the blood using both as tools.

Part One: Introduction to the Beck Protocol...
http://video.google.ca/videoplay?docid=3879823462993133294

Part Two: How to Use the Beck Protocol...
http://video.google.ca/videoplay?docid=-3494194760973110305


Take a look at what you'll find about Tetrasil.

http://www.google.com/search?hl=en&q=tetrasil,aids&btnG=Google+Search&aq=f&oq=tetrasil,aid



On the lookout for ways to improve the effectiveness of what was becoming known as “The Beck Protocol,” Bob Beck started ozonating his drinking water with a device he built using parts from a pet supply store for ozonating fish tanks. Using a pulse oximeter to measure oxygen levels in blood and experimenting with friends, he found the oxygen level of the blood could be improved by drinking ozonated water. Ozone, of course, is known as a powerful oxidizer so he knew it would be a step to help flush toxins from the body. The Beck Protocol now consists of four tools using three units—one that offers both blood electrification and making ionic/colloidal silver, one that offers lymph and tissue electrification and the third is a water ozonator.

Can you imagine that people can treat themselves with this effective treatment for barely paying anything for their health?

 

[Magicman]

I've known about Ozone (and food grade peroxide) for years. Also look at anti-angeogenesis drugs and feverfew (parthenolide) for killing cancers of all sorts, as well as curing migraines, macro-degeneration, leprosy, inflammatory bowel disease and other maladies.

They'll remain in "clinical trials" for eternity, or just be outlawed. Clinical trials are just rigged-to-fail charades. You have to be clinically dead to qualify.

My father's been dead almost nine years now, and they have yet to begin the anti-angiogenesis trials they had him sign up for in 2000, which were only to be conducted in tandem with chemotherapy drugs.

In this country, it's every man for himself.

Thanks for posting the info. It's a great subject that gets zero press.

Bosso

I'm sorry to hear about your loss. I hope maybe this method will get out more so there will be an overall change in the mentality of the medical business.


Does anyone who have experience with oxidative-based methods know how it could help a condition like fibromyalgia or lessen trigger points?

This man has claimed he has treated himself completely free with Ozone Therapy with a process of 'self-healing'. His site is a bit quirky but he's genuine and isn't looking out for money. Kind've interesting because his philosophies are completely the opposite of how most people approach their condition with fibromyalgia.

That's what I've had for the past 4 years so when I found this site and saw similar methods as I've been discovering and attempting; since most conditions seem to fall on similar levels based on 'oxidative stress'. The treatments he used reinforced that belief of 'self-healing' process.

http://falconblanco.com/health/index.htm