(Feb 2000)
Written by
Mark G Lester
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Whilst Oxygen therapy is an umbrella term for over 50 different methods that all seek to de-toxify the body by flooding it with oxygen, Ozone therapy is the most researched and widely used medical technique for achieving this goal. Ozone is an activated, trivalent (three atoms) form of oxygen. Oxygen is O2 whereas ozone is O3. Medical Ozone is made when Medical Grade Oxygen is electrically activated (using an Ozone Generator) to form Ozone. Ozone is virucidal, germicidal, bactericidal, and fungicidal. Oxygen has these properties too, but less strongly.
The number of published papers, spanning 130 years, on the benefits of Ozone
therapy now number in the thousands. One relatively recent paper is Ozone
Selectively Inhibits Growth of Human Cancer Cells.1 Note the use of
the word “selectively” meaning “without harming healthy cells”. Another recent
paper reported that “Ozone was found to inactivate HIV”.2 Dr Michael
Carpendale et al, working on the AIDS virus found that they could produce an
enormous inactivation of the virus, reducing it from a million virions down to
no viruses at all at about 4 micrograms of ozone, with twice that dose having
no adverse effect on healthy white blood cells.3
Sixty patients with osteoarthritis at the Center of
Medical- Surgical Studies in Havana (mostly affecting the knee) were given one
interarticular injection of ozone per week for a total of ten weeks. Of the
sixty patients, only four experienced the return of painful symptoms after two
months, while the majorities (93.3%) were symptom free.4
Otto Warburg is the only man in history to win the Nobel Prize for Medicine twice. His research on cancer for which he was awarded the prize led him to the conclusion that “Cancer has only one prime cause. It is the replacement of normal oxygen respiration of the body’s cells by an anaerobic (i.e. oxygen-deficient) cell respiration”.5
Ozone therapy itself is subdivided into a number of
different methods, some of which can be self-administered with an Oxygen
cylinder and a medical Ozone generator. These methods include Ozonating water
(useful for bladder, stomach and kidney problems in particular),
vaginal/bladder insufflation for reproductive and genito-urinary problems, ear
insufflation for problems of the ears, eyes, sinuses and brain, and rectal
insufflation for problems of the colon. Medical doctors tend to favour
auto-haemotherapy where blood is taken from the body, mixed with Ozone and then
returned to the body (this is used commonly in Germany), and direct
intra-venous injection. One more advanced method for using Ozone is polyatomic
apheuresis, which is similar to auto-haemotherapy, but with this method the
blood is continuously fed back to the patient, rather like dialysis.
I believe that all of the above methods work and save
lives. However, the method I favour and use most is known as Transdermal Ozone
therapy. This is a method in which Ozone is introduced into the body via the
skin while sitting in a hot steam cabinet. As the pores of the skin open as
result of being surrounded by the warm steam, Ozone enters the body
transdermally (i.e. via the skin). This method is not new: Dr. Kellogg first
used ozone in steam saunas at his naturopathic clinic in Battle Creek, Michigan
as far back as 1881. The transdermal method has a number of advantages over the
other methods:
1) It treats the whole body simultaneously;
2) The steam sauna has its own de-toxifying
effects in addition to the de-toxification induced by Ozone;6,7
3) Transdermal Ozone cleanses the lymph. 90%
of body fluids are stored in the lymph, which is superficial, lying just under
the skin, only moving around the body once every 24 hours. Transdermal Ozone
will cleanse and de-toxify this often sluggish system;8
4) This method does not involve injections
or needles, does not need the administration of a medical doctor, tends to be
cheaper for the clients than methods that only a doctor may use legally, and is
both profoundly relaxing and enjoyable for the client.
Transdermal/hyperthermic Ozone therapy has been proven to have a powerful oxygenating effect on the body. The paper Quasi-total body exposure to Oxygen/ Ozone in a sauna cabinet (1999) concluded that hyperthermic ozone induced a “statistically significant, rapid increase of venous pO2 (partial pressure of Oxygen)”. It further concluded that TBARS (another measurement of Oxygenation of the blood) “increase steadily”.9
ME and all of cases of low vitality are conditions I have seen Ozone therapy get especially consistent results with. Almost everyone comments on how much more energy they have within a few sessions. There have also been benefits for multiple sclerosis, diabetes and digestive problems; in fact, the range of benefits is for any condition where the main cause is toxins in the body.
Case Studies
Dee has been suffering with multiple sclerosis since 1991.
Because one needs to be very cautious with MS in using heat, I only allowed her
10 minute sessions in the ozone steam sauna to begin with and built the
treatment time up gradually. I also used 5 minutes of ear insufflation in each
ear to help improve her balance. Whilst Dee is not “cured” weekly sessions over
six months have given her, in her words “a massive boost of energy, my brain is
clearer and my balance has improved so that I recently ran for the first time
in 7 years”.
Dee Dee, (not related to previous case study) an ex model, was
a silicon sufferer. This disease is caused by breast implants leaking and
releasing toxins throughout the body, causing symptoms similar to rheumatoid
arthritis, including severe joint pain, shooting pains in her chest, numbness
and weakness in her arms and legs, sleeplessness, constant tiredness and
migraines. Much to my own astonishment, she reported after one session that 90%
of her symptoms had disappeared. At the time of writing she has had 4 sessions
and describes herself as 95% better.
References
1 Sweet F et al. Ozone Selectively Inhibits Growth of Human Cancer
Cells Science 209(22): 931-933. Aug 1980.
2 Latino J et al. Inactivation of Human
Immunodeficiency Virus Type 1 by Ozone in Vitro. In Blood the Journal of
the American Society of Haematology 78(7). 1 October
1991.
3 Ozone and the Politics of Medicine. Video. Threshold Film
Inc. August 1993.
4 Altman N. Oxygen Healing Therapies Second Edition.
Chapter 7, page 138. Translation. 1998.
5 Warburg O. The Prime Cause and Prevention of Cancer.
Lecture delivered to Nobel Laureates, Lindau, Lake Constance, Germany 30 June
1966.
6 Clinical experience with hyperthermia. Indiana University
Medical Centre. Journal of Oncology. 1993.
7 Valley Cancer Institute 304-12099 W. Washington Blvd, Los
Angeles California.
8 Pressman S. The Story of Ozone. 1995.
9 Bocci V et al. Quasi-Total Body Exposure to
Oxygen/Ozone in a Sauna Cabinet. Institute of General Physiology,
Institute of Cardiovascular Surgery, University of Sienna, 1999.
Recommended reading
1 McCabe E. Oxygen Therapies: A new way of approaching
disease. Energy Publications
ISBN 0-9620527. 1988 .
2 Altman N. Oxygen Healing Therapies. Second Edition
Healing Arts Press
ISBN 0-89281-793-3. 1998.
3 Rilling S and Viebahn R. The Use of Ozone in Medicine.
Haug Publishers. English Edition
ISBN 3-7760-0956-X. 1987
4 Pressman S. The Story of Ozone. This book has no
ISBN but is available from the Finchley Clinic.
1995.
About the Author
Mark Lester is an holistic therapist who has been researching the
benefits of Ozone therapy since his mother’s death from endometrial cancer in
1997. In his practice Mark also uses PIP scans, Electro-Crystal therapy, Bowen
technique, Rife treatment, Nutrition and Remedial Massage. He runs the Finchley
Clinic in North London and can be contacted on 020 8-349 4730. His web site is www.the-finchley-clinic.co.uk
Editor’s Note
The field of oxygen therapies has always been controversial; however progress continues to be made. We welcome comments from practitioners in the field regarding their clinical experiences with oxygen therapies.
Therapies are available under the supervision of Mark G. Lester from:
The Finchley Clinic,
26 Wentworth Avenue,
London N3 1YL
+44(0)20 8349 4730
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