Why we should not trust a medical system that needs sickness to support and grow its bottom line.

Iatrogenesis is the third leading cause of death in the USA after heart disease and cancer. Most recent estimates are that over 200,000 deaths each year are attributable to medications not performing like they are intended. Iatrogenous disease does not include cases of malpractice.

AS the movie Doctored point out, there are many many alternatives — exemplified by successful early treatment options for SARS-CoV-2 that were forbidden by the NIH-FDA-CDC-Pharma machine. Here are a couple examples of therapies that could have been employed.

Ultraviolet Irradiation of Blood: “The Cure That Time Forgot”?

Michael R. HamblinAuthor informationCopyright and License informationDisclaimerThe publisher’s final edited version of this article is available at Adv Exp Med BiolSee other articles in PMC that cite the published article.Go to:

Abstract

Ultraviolet blood irradiation (UBI) was extensively used in the 1940s and 1950s to treat many diseases including septicemia, pneumonia, tuberculosis, arthritis, asthma and even poliomyelitis. The early studies were carried out by several physicians in USA and published in the American Journal of Surgery. However with the development of antibiotics, UBI use declined and it has now been called “the cure that time forgot”. Later studies were mostly performed by Russian workers and in other Eastern countries and the modern view in Western countries is that UBI remains highly controversial.

This chapter discusses the potential of UBI as an alternative approach to current methods used to treat infections, as an immune-modulating therapy and as a method for normalizing blood parameters. No resistance of microorganisms to UV irradiation has been reported, and multi- antibiotic resistant strains are as susceptible as their wild-type counterparts. Low and mild doses of UV kill microorganisms by damaging the DNA, while any DNA damage in host cells can be rapidly repaired by DNA repair enzymes. However the use of UBI to treat septicemia cannot be solely due to UV-mediated killing of bacteria in the blood-stream, as only 5–7% of blood volume needs to be treated with UV to produce the optimum benefit. UBI may enhance the phagocytic capacity of various phagocytic cells (neutrophils and dendritic cells), inhibit lymphocytes, and oxidize blood lipids. The oxidative nature of UBI may have mechanisms in common with ozone therapy and other oxygen therapies. There may be some similarities to extracorporeal photopheresis (ECP) using psoralens and UVA irradiation. However there are differences between UBI and ECP in that UBI tends to stimulate the immune system, while ECP tends to be immunosuppressive. With the recent emergence of bacteria that are resistant to all known antibiotics, UBI should be more investigated as an alternative approach to infections, and as an immune-modulating therapy.

Keywords: Ultraviolet C, Knott hemo-irradiator, UBI, DNA repair, Blood cells, Antigen-presenting cells, Infections, Cytokines

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TREATING HIV/AIDS WITH OXYGEN

What Doctors Don’t Tell You2 min read

In 1991, Dr Michael Carpendale and his colleagues at the Veterans Administration Hospital in San Francisco showed that HIV could be 99 per cent inactivated using only 0.5 mcg ozone/mL of human blood, and completely inactivated by concentrations of 4 mcg/mL of human blood, neither of which were harmful to healthy cells (Antiviral Res, 1991; 16: 281-92). Early studies by the team had indicated that ozone could boost T-cell counts and eliminate infection for more than five years (Ozone in Medicine: Proceedings of the 11th Ozone World Congress, Stamford, Conn: International Ozone Association, 1993).

Another American study in vitro found that ozone completely deactivated a cultured cell medium containing HIV-1 without causing significant damage to non infected cells (Blood, 1991; 78: 1882).At Moscow’s Institute of Virology, scientists used a concentration of 4 mg/mL of ozone on an HIV infected culture. Within minutes, the cell containing the virus had decomposed and died (Kornilaeva GV et al, in Ozone in Biology and Medicine, Nizhni Novgorod, 1992, p 86).

A study by the Canadian Armed Forces to determine the ability of ozone to kill HIV, hepatitis viruses and herpesvirus in blood for transfusion found that three minute ozonation of blood spiked with one million HIV-1 particles per millilitre achieved 100 per cent deactivation of the virus (Can Med Assoc J, 1993;148: 1155-60).

Another study of five AIDS patients by Dr Frank Shallenberger resulted in an immediate increase in T cells, relief of symptoms of opportunistic infections and higher energy levels with ozone treatment (Proceedings of the 4th International Bio-Oxidative Medicine Conference, Oklahoma City, IBOM, 1993).

According to a German study of 27 patients by Dr Horst Kief, who pioneered the development of autohomologous immunotherapy (AHIT) using ozone, 80 per cent of the patients survived more than 18 months and 70 per cent more than 45 months with his treatment. This represents a much higher percentage than those treated conventionally (Ozone and the AHIT Therapy in AIDS Patients, Ludwigshafen, Kief Clinic, 1993).

At present, Dr Juliane Sacher of Frankfurt has one of the largest medical practices treating AIDS patients with ozone.

Ozone – Oxygen Therapies

by Nathaniel Altman, Author of the book Oxygen Healing Therapies

Q; What types of diseases can be treated with ozone and hydrogen peroxide?
A: Bio-oxidative therapies offer a tremendous range of medical applications. According to the International Bio-Oxidative Medical Foundation (IBOMF), an Oklahoma-based organization devoted to research and education about these therapies, the following conditions or diseases have been treated with ozone and hydrogen peroxide with varying degrees of success:

Heart and Blood Vessel Diseases
Peripheral vascular disease (poor circulation)
Cerebral vascular disease (stroke and memory loss)
Cardiovascular disease (heart disease)
Coronary spasm (angina)
Cardioconversion (heart stopped)
Cardiac arrhythmias (irregular heartbeat)
Gangrene (of fingers and toes)
Raynaud’s disease (“white finger”)
Temporal arteritis (inflammation of the temporal artery)
Vascular and cluster headaches
Pulmonary Diseases
Chronic obstructive pulmonary disease
Emphysema
Asthma
Bronchiectasis (dilatation of bronchus or bronchi)
Pneumocystis carinii (PCP or AIDS-related pneumonia)
Chronic bronchitis
Infectious Diseases
Influenza
Herpes zoster (shingles)
Herpes simplex (fever blister)
Systemic chronic candidiasis (candida)
Epstein-Barr virus (Chronic Fatigue Syndrome)
HIV-related infections
Acute and chronic viral infections
Chronic unresponsive bacterial infections
Parasitic infections
Immune Disorders
Multiple sclerosis
Rheumatoid arthritis
Diabetes mellitus Type II
Hypersensitive reactions (environmental and universal reactors)
Other Diseases
Parkinson’s Disease
Alzheimer’s Disease
Migraine headaches
Chronic pain syndromes (due to multiple causes)
Pain of metastatic carcinoma
Cancers of the blood and lymph nodes 4

Q: Is it true that ozone cures AIDS?

A: There is growing evidence that ozone (as well as hydrogen peroxide, since ozone becomes transformed into hydrogen peroxide in the body) can destroy lipid-enveloped viruses both outside and within the body, including those related to hepatitis, Epstein -Barr, cancer, herpes, cytomegalovirus and HIV. The results of a study coordinated by the Canadian Armed Forces and published in the Canadian Medical Association Journal showed that ozone kills HIV, the hepatitis and herpes viruses, and other harmful agen ts in the blood used for transfusion. The author of the article added, “The systemic use of ozone in the treatment of AIDS could not only reduce the virus load, but also possibly revitalize the immune system. ” 5 Although a related study on AIDS patients proved inconclusive, Cmdr. Michael Shannon, MD, one of the coordinators of the study, wrote that “Of interest, however, the three patients (out of ten volunteers) who responded to minor autohemotherapy in the first trial, are still alive after four years p ost treatment, with CD4 counts in excess of two hundred. These patients should have theoretically succumbed to AIDS within a year post-treatment.”6 In several clinics in Germany, AIDS patients are being treated successfully with different types of ozone t herapies, including rectal insufflation, ozone bagging, and autohemotherapy.

Although used by an estimated ten million patients in Europe since the early 1960’s, the therapeutic use of medical ozone and hydrogen peroxide (technically known as “bio-oxidative therapies”) is largely a mystery to North Americans. Hailed as a safe, eff ective and low-cost treatment for a wide spectrum of diseases- including candida, cancer, heart problems and HIV- related infections- in Europe, proponents feel that they can go far in resolving America’s health care crisis. However, physicians who have tr ied to utilize these therapies in this country are often harassed by local medical societies and threatened with loss of license. As a result, every year hundreds of patients have been forced to seek out physicians in Germany, Russia and even Cuba where t hese therapies are an accepted part of the medical mainstream.. Others spend tens of thousands of dollars to receive bogus ozone cures from unlicensed practitioners here and abroad who ignore established protocols. Many end their lives in both poverty and despair.

What is the truth behind bio-oxidative therapies? Are they a panacea to our health-care crisis, or are ozone and hydrogen peroxide ineffective and even dangerous to health? And despite decades of clinical success, why are they considered “experimental” an d not approved by the FDA? On the following pages, let’s examine some of the major questions about bio-oxidative therapies and their role in human health care picture.

Q: Exactly what are bio-oxidative therapies?
A: Bio-oxidative therapies involve administering small amounts of diluted ozone and hydrogen peroxide into the body for the prevention and treatment of disease. Ozone therapy has been used by licensed physicians in Germany since the early 1960’s, while hydrogen peroxide therapy was developed in the United States primarily by Dr. C.H. Farr, nominee for the 1993 Nobel prize in Medicine.

Q: What is the scientific basis for bio-oxidative therapies?
A: The philosophy behind bio-oxidative therapies is a simple one. The use of hydrogen peroxide and ozone in medicine is based on the belief that the accumulation of toxins in the body is normally burnt up by the process of oxidation, a process wherein a s ubstance is changed chemically because of the effect of oxygen on it. Oxidation breaks the toxins down into carbon dioxide and water, and eliminates them from the body. However, if the oxygen system of the body is weak or deficient (whether through lack o f exercise, environmental pollution, poor diet, smoking, or improper breathing), our bodies cannot eliminate them adequately and a toxic reaction can occur. In minor cases, a toxic buildup can lead to fatigue, while a wide range of diseases can result when poor oxygenation is chronic.

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