Mission Clinic

“Whether you are aware of it or not, our body emits measurable bio-energetic waves (bio-electromagnetic body field) all around us. This is what worldwide Traditional Medical Practices have been aware of for thousands of years, calling this energy by different names such as Chi (Chinese Traditional Medicine), Prana (Indian Traditional Medicine), Ka (Ancient Egyptians), Aura (Western Cultures) and others. 

Acupuncture (Bio-Energetic Medicine) is coming of age due to our understanding of Quantum Physics, the ability to measure this energy and understanding the relationship between our electromagnetism and our physiology. Acupuncture unblocks and corrects the informational-energetic body fields (meridians) enabling our body to use its fabulous innate intelligence to heal itself.
Informational-energetic changes occur before disease is manifested in overt physical signs, symptoms, abnormal laboratory values and imaging studies are able to detect them. Acupuncture, therefore, has the very real potential to prevent pre-mature illness and maintain health.

Our Acupuncture Meridian Assessment and Acugraph devices provide an objective and accurate quantification system which allows us to verify the efficacy of our point selection(s), ensuring the optimal diagnosis and treatment. In this way, both practitioner and patient actively participate in the healing process.”

The idea of using electricity, generated by a torpedo fish, to treat neurological and other disorders dates back to the Roman Empire. However, it was not until the 18^th Century that advances in understanding electricity, combined with technological advances in electrical devices, made electrotherapy a real possibility. One of the theories that gained a widespread following was that of “animal electricity”, a term coined by Luigi Galvani to indicate the inherent electricity in the nervous system of all animals, including humans, that was the “animating force” of life. Galvani’s theory came from his observations of movement in the legs of dead frogs using electrical charges.

Physicians and inventors such as Otto von Guericke, Johann Gottlob Kruger and others continued to experiment with electrical applications in medicine. One of the out-front physicians touting the benefits of electricity in medicine was the itinerant physician Dr. T. Gale. He proclaimed the importance of electricity for the future of medicine in the first American handbook in 1802, ‘Electricity or Etheral Fire, Considered”, on the theory and practice of medical electricity

Advances continued slowly in electric medicine with the discovery of antibiotics and other modern medicines. However, in 1991, two physicians - Drs. Steven Kaali and William Lymann - from Albert Einstein’s College of Medicine presented a paper at the First International Symposium on Combination Therapies, March 14^th, 1991, in Washington D.C. that documented the ability of microcurrents to disable bacteria, viruses and other blood pathogens without harming healthy tissue. After learning of the discovery, Bob Beck, a retired physicist, reasoned that with the correct instrument the blood/ circulatory system could be electrified through the skin. Hence Bob Beck’s blood electrification protocols were born.

We are, at our base, purely electrical in nature; our bio-chemical and physical form/structure is nothing more than the physical representation of our “energetic self”. Pulsing electrical microcurrents (gentle currents that both stimulate and nourish our natural energetic system) into our blood either percutaneously via the wrist arteries/veins (closet vessels to the skin) or directly into blood, can stimulate and enhance our body’s innate electrical and hence self-healing mechanisms.

Advantages of blood electrification:

• Reduces blood pathogens - the discovery that lead to the Nobel Prize in Medicine went to, two Australian physicians who discovered that stomach ulcers and stomach cancer are caused by the bacterium, H. pylori. This fact has given credence to what many physicians and scientists believe; that is that many diseases that we say are of unknown origin or cause, are actually the result of chronic infections. These diseases include cancer, Multiple sclerosis, Alzheimer’s, most auto-immune diseases, most neuro-degenerative diseases, heart diseases and many others.
• Increases energy production
• Supports the immune system
• Supports all cellular functions
• Calming effect by balancing the sympathetic and parasympathetic nervous systems.
• Free electrons are the ideal anti-oxidants, agents that neutralize harmful free radicals, which are responsible for most disease and the chronic degenerative changes of pre-mature aging.
• Increases detoxification
• Increases circulation
• Accelerates healing

We use blood electrification combined with PEMF (pulsed electro-magnetic field) therapy, ozonated water and colloidal silver to enhance our blood electrification protocols.

Dichloroacetic acid or DCA - DCA disrupts cancer cell energy production. Cancer cells primarily produce energy using large amounts of sugar (glucose) and small amounts of oxygen, this is basically fermentation. DCA blocks this primary mechanism of cancer cell energy production and if a cell cannot produce energy it will die. In addition, DCA also targets cancer stem cells (CSCs) which are the primary cause of cancer metastasis.

Oxaloacetic acid - As stated above, glucose (sugar) is the primary energy source of cancer cells, however, a secondary source is amino acids, specifically glutamine. Oxaloacetic acid does to cancer cell glutamine metabolism what DCA does to cancer cell sugar metabolism. That is, oxaloacetic acid blocks cancer cell utilization of glutamine for energy production. Oxaloacetic acid is also an excellent anti-aging therapy, the benefits are:

• Increase in average and maximal lifespan
• Decrease in cancer incidence, up to 55%.
• Decrease in neurodegenerative diseases such as Alzheimer’s and Parkinson’s Diseases.
• Protection against Type II Diabetes Mellitus
• Reduction in cardiovascular risk, especially arthrosclerosis.
• Reduction in inflammatory/auto-immune diseases.

Painful conditions of the knee, hip, foot, shoulder and elbow are extremely common maladies due to accidents, athletic injuries and the wear of an aging population. There are numerous causes of joint pain ranging from obesity, underlying infections, meniscus tears, cartilage injury and ligament strain. However, the most common cause of painful joints is osteoarthritis, which is an inflammatory condition characterized by denuded or absent joint cartilage and inflamed synovial fluid.

If any local or systemic issues such as bone fractures, infectious diseases, cancer, autoimmune diseases have been identified, they must be addressed prior to any joint injections.

Once it has been determined that a joint injection would be appropriate, we utilize a number of anti-inflammatory and regenerative techniques to alleviate pain and, hopefully, regain optimal function:

• Ozone
• Prolozone (ozone, procaine, dextrose)
• Autologous ozonated blood
• Autologous ozonated bone marrow

Female pelvic pain due to uterine fibroids:

Uterine fibroids are benign growths that develop from the muscle tissue of the uterus are a major cause of female pelvic pain and bleeding. However, other causes include:

• Cancer
• Infections
• Inflammation
• Pelvic/spinal nerve dysfunction and cancer.

Depending on the cause we usually administer a combination of the following:

• Ultrasound guided direct ozone/mistletoe/local anesthetic injection of the fibroids
• Subcutaneous mistletoe injection
• Rife Therapy
• Anti-microbial therapies
• Bladder instillation of DMSO, procaine and ozone
• Spinal/subarachnoid neural therapy injections.
• Salicinium therapy

The prostate gland is located just below the bladder in men and surrounds the top portion of the tube that drains urine from the bladder (urethra). The prostate's primary function is to produce the fluid that nourishes and transports sperm (seminal fluid).

Disease of the prostate gland usually occurs after the age of forty years, however, the incidence of prostate disease is increasing in younger age groups. Diseases that affect the prostate gland are:

• Inflammation - Enlarged or Benign Prostatic Hypertrophy
• Infections - Prostatitis
• Cancer
• Pelvic/Spinal Nerve Dysfunction - Prostate pain or prostadynia

Male pelvic pain can also be due to:

• Bladder dysfunction - Interstitial cystitis
• Bladder infections
• Infections of the urethral tract

We use a number of therapies for male pelvic pain such as:

• Ultrasound guided direct ozone/mistletoe/local anesthetic injection of the prostate gland
• Subcutaneous mistletoe injection
• Rife Therapy
• Anti-microbial therapies
• Bladder instillation of DMSO, procaine and ozone
• Spinal/subarachnoid neural therapy injections.
• Salicinium therapy

We have two nervous systems, the central (CNS) and the peripheral (PNS) nervous systems. The PNS is further divided into the autonomic (ANS) or vegetative nervous system and the enteric (gastro-intestinal) nervous systems.

The ANS is further divided into the sympathetic (fright, fight and flight) and para-sympathetic (rest, relaxation and repair) nervous systems. See chart below:

The central nervous system which consists of the brain and spinal cord is the more well-known system. However, the autonomic nervous system is actually much “older” than the central nervous system as it evolved much earlier to control our physiologic processes. The ANS regulates involuntary physiologic functions such as heart rate, blood pressure, respiration, digestion, sexual function and especially chronic pain. That is, the ANS regulates the functions of our internal organs such as our stomach, heart, lungs and intestines.

The autonomic system reaches every cell in the body via peripheral nerve ganglia, nerve plexus and assorted peripheral nerves. We access this system via injections into the spinal/epidural space, nerve ganglia and plexus:

• Lower-Back (lumbar) Spinal and Epidural spaces - Three layers of tissue cover the spinal cord called the pia mater (which is directly attached to the spinal cord), the arachnoid mater (the middle layer) and the dura mater (the outermost layer). The epi-dural space is the area directly outside or “above” the dura mater; the spinal or sub-arachnoid space is the area just below the arachnoid mater. The subarachnoid space contains the spinal fluid or cerebral spinal fluid which covers the entire brain and spinal cord.
• Nerve Ganglia - Ganglia can be thought of as a relay station between groups of nerves. They are a collection of neuronal bodies that run along the entire spinal cord and some extend outward toward some organs. These are the primary transmission stations for the autonomic nervous system, e.g. the Stellate ganglion in the neck and the pelvic ganglia located closer to the reproductive organs.
• Nerve Plexus - These are dense networks of intersecting nerves (primarily motor and sensory) - usually covered by connective tissue - that affect specific areas of the body. For example, the brachial plexus controls the shoulder, arms and hands and the femoral/sacral plexus controls the entire lower extremity.
• Peripheral Nerves - These are usually single or smaller groups of nerves that branch directly from the spinal cord.

Please note, we routinely separate the functions of the different nerve groups based on function such as motor, sensory, mixed, sympathetic or parasympathetic. However, the truth is that all these nerves are connected in order that our body functions as a cohesive whole.

An “Interference Field” is the term applied to disruption or blockage of the autonomic or vegetative nervous system (and by extension the bio-energetic field) by trauma, injury, toxins, infection or a combination of these and other factors. This disruption can result in the continuous transmission of pain signals long after the original injury is healed resulting in pain, fatigue, disability and an inability to heal.

Epidural, spinal and neural (ganglia, plexus and peripheral nerves) therapy injections are employed to alleviate pain, disability and also positively affect organ function by removing the impediments to proper functioning of the autonomic nervous system. That is, they remove the interference field by the injection of substances that reduce inflammation, repair affected nerves, enhance immune function and re-set (similar to re-booting a computer) affected segments of the autonomic nervous system.

Please note that interference fields may also exist in scars (from previous injury or surgery), glands, teeth and other tissue. These areas may also be injected with the result being normalization of illness-related nervous system dysfunction and an immediate and dramatic relief of pain, feeling of euphoria and emotional release.

Of the thousands of molecules that make up a cell, phosphatidylcholine (PC) is one of the most important and possibly, the most important molecule. PC is the primary substance of each cell’s membrane. The cell membrane is analogous to our skin that surrounds our body. However, in each cell there are essential sub-cells - mitochondria, nuclei and others - within the cell, and each one of these sub-cells has a similar cell membrane. The cell membrane can be looked at as the “Biochemical Essence of Life”, because other components of a cell may be damaged and the cell will live, however, if the cell membrane is damaged there will be immediate cell death. That is, if the cell membrane of a brain/spinal cord cell, heart cell, liver cell, immune cell is damaged, that function will cease to exist.

PC acts primarily on the heart and vascular/circulatory system by the following mechanisms:

• Reducing the LDL/HDL cholesterol ratio
• Binds and removes cholesterol/cholesterol plaque from tissue
• Reduces abnormal serum triglyceride levels
• Detoxifies the entire system
• Optimizes cell membrane bound enzyme systems
• Improves blood and microcirculation flow due to its incorporation in red blood cells and platelets.

The vascular system is ubiquitous, that is, it goes to every cell in the body because of its essential function of delivering oxygen and nutrients and removing waste. Therefore, because phosphatidylcholine acts primarily on the vascular system, it enhances all organ functions.

Phosphatidylcholine is primarily indicated in heart/blood vessel disease, wound care, neurological disease (Parkinson’s, Alzheimer’s, MS, ALS, post-stoke and others) and liver disease. However, because of its broad spectrum of activities it is used in anti-aging medicine, detoxification, kidney disease and many others.

Insulin potentiation utilizes insulin’s ability to reduce blood sugar as a “Biologic Response Modifier (BRM)”. That is, insulin’s ability to reduce blood sugar enhances the effectiveness of many drugs, including anti-cancer agents. This leads to greater drug efficacy with less side-effects.

Potential mechanisms of insulin-induced hypoglycemia. Cancer cells have, on average, 5-20 times as many GLUT or glucose receptors as normal cells. Therefore, insulin induced hypoglycemia results in cancer cells become extremely “hungry” because there is no sugar to utilize. This “hunger” leads to maximal activation of their GLUT receptors and a large increase in trans-membrane passage/anti-cancer drug uptake by cancer cells.

An additional benefit on insulin induced hypoglycemia in anti-cancer therapy, is that low-blood glucose levels ensure that cancer cells are “awake”, in a state of maximum metabolism/replicating state (S-Phase of the replicative cycle). A huge issue with just giving chemotherapy without regard for the metabolic state of cancer cells is that, if the drugs are administered when the cancer cell is “asleep” the drugs will not be absorbed into the cancer cell but be absorbed primarily into normal cells leading to the well-known adverse effects of chemotherapy (nausea, vomiting, hair loss, gastro-intestinal ulcers, low blood counts, etc.). IPT activates the cancer cells and this along with increased transmembrane passage, leads to much greater anti-cancer drug efficacy.

In addition to the above, insulin induced hypoglycemia results in the following beneficial effects.

1. Increased tissue/blood oxygenation. This may be a relative increase due to the decreased carbohydrate quantity and therefore decreased utilization of carbohydrates.
2. Increased tissue/blood pH (alkalization) via the same mechanism as above.
3. Hypoglycemia leads to elevated body temperature which optimizes white blood cell/immune function.
4. Because of the above mechanisms, most drugs can be given at 10-20% of their normal dose resulting in little-no side-effects.

Note well, the above factors are at play in the treatment of cancer, acute myocardial infarctions, cerebrovascular accidents, perioperative cardiac/vascular patients for cardiac/non-cardiac surgery, etc.

Salicinium demonstrates broad, potent, anti-viral and anti-cancer properties via the following mechanisms:

1. Disrupting cancer metabolism/energy production
2. Potentiating healthy immune function
3. Disrupting the synthesis of the immune-suppressive enzyme nagalase.

Disruption of Cancer Cell Energy Production - Cancer cells are primarily dependent on sugar and fermentation (glycolytic metabolism) for energy to survive. Salicinium directly inhibits cancer cell fermentation (pushing it away from glycolysis to normal cell oxidative phosphorylation) and therefore energy production, leading directly programmed cancer cell death (apoptosis).

GLUT Receptors. All cells have GLUT receptors to transport sugar for energy production. However, because cancer cells are dependent on sugar for energy, they typically over-express GLUT receptors and usually have 5-20 times more GLUT receptors than normal cells. These receptors lead to enhanced uptake of compounds such as salicinium leading to enhanced disruption of cancer cell metabolism.

Disruption of Nagalase Synthesis. Gc protein, which is produced normally, is converted to GcMAF (Gc Macrophage Activating Factor). GcMAF enhances the ability of macrophages (an important immune cell) to both recognize (immune surveillance) and destroy cancer cells.

Nagalase is an enzyme that is produced by cancer cells (and viruses) that inhibits Gc protein from being converted into GcMAF. This results in our immune system being unable to recognize cancer (immune evasion) and therefore unable to destroy cancer cells by one of our most important immune cells. Nagalase also degrades the extracellular matrix of the normal cellular environment enabling cancer cells to invade. Salicinium disrupts nagalase synthesis and thus cancer cells are unable to evade our immune system.

Enhanced Immune Function - Macrophages are important in downstream activation of NK or Natural Killer cells. NK cells are specialized cancer killing and because salicinium prevents nagalase production, it enables macrophages to properly activate NK cells which further destroy cancer cells.

Please note, salicinium does not kill malignant cells directly, it optimizes immune system so that it can do its job.

In addition to being a cancer treatment therapy, mistletoe is now used in as a cancer preventative. This course of prophylaxis is not a matter of inoculation in the customary sense where vaccines are produced for mass inoculations. Mistletoe cancer prevention inoculation is an individualized mistletoe injection based on the patient’s particular personality, organ at risk, physical and mental characteristics.

We know that cancer begins developing five, ten and possibly twenty years before there are overt signs and symptoms. A pre-cancerous stage occurs primarily in the early-mid forties to mid-fifties (or younger based on symptoms) usually coinciding with major life changes such as pending retirement, divorce, empty nest, job loss, death of a loved one, major accidents, abrupt changes in health and other life-changing events.

The following are risk factors that should be discussed with the prescribing physician:

1. Persons with a genetic predisposition to cancer
2. Persons with a strong family history of cancer
3. Cancer patients in remission
4. Pre-cancerous symptoms:

• a. Obesity
• b. Constantly feeling cold, shivering and almost never feeling warm
• c. Tiredness, often to the point of exhaustion.
• d. Difficulty in falling asleep and frequently awakening throughout the night
• e. Constant night sweats.
• f. An increase in warts and other skin lesions.
• g. Attacks of dizziness
• h. History of smoking more than 10-cigarettes a day.
• i. Psychological traumas e.g. serious illness, death of a spouse, divorce, loss of employment/ financial difficulties and other events that cause mental stress.

The therapeutic regimen consists primarily of once weekly subcutaneous injections (under the skin like insulin injections in diabetics) for seven-weeks, a one-week break, followed by another seven-weeks of injections. Intravenous injections may be added if needed in the opinion of the physician.

Most people are extremely surprised to learn that Mistletoe - the curious holiday decoration - is one of the most well studied natural medicines in the world. They are even more surprised that in many parts of Europe – primarily Germany and Switzerland – Mistletoe therapy is prescribed for over 60%of cancer patients. Furthermore, the treatment is paid for by health insurance companies and is therefore approved by their health regulatory agencies.

Mistletoe is primarily used as an adjunct or add-on/complementary therapy to enhance the effects of standard of care or conventional cancer therapies.

In addition, it is used to reduce the risk of cancer recurrence in cancer survivors and as a cancer prevention measure in persons at increased risk for cancer. Such as persons with a genetic predisposition to cancer and those with a strong family history of cancer.

Long before it showed up in holiday traditions, mistletoe was highly regarded in Norse and Greek Mythology. Mistletoe appeared as a key or wand allowing legendary heroes to travel safely back and forth between the land of the living and the Underworld.

The ancient druids (priests, magicians and soothsayers in the ancient Celtic religion) used mistletoe as a promoter of fertility and longevity.

Early European herbalists recommended mistletoe for epilepsy and as a sedative, especially for those who had suffered great loss.

Though mistletoe had many applications in early herbal medicine, it has taken thousands of years to unlock the modern secrets of mistletoe.

Over centuries, Western medical literature accumulated stories of cancer patients developing feverish infections, eventually overcoming the infection and having their tumour shrink or go into total remission. These “developments” were early clues regarding immunotherapy. Only in recent years would researchers link the role of warmth and immune-modulation as a potential cancer therapy. The infection induced fevers seemed to heighten immune activity which led to a breach of the cancer’s microenvironment and elimination of the cancerous cells.

Today, because of scientific advancement, we have identified mistletoe’s primary medicinal constituents. These include, but in no way are limited to inflammatory (warmth inducing) lectins, viscotoxins, anti-inflammatory flavonoids and substances that interact with nerve cell – GABA – receptors that have a calming or sedative effect. Primarily the viscotoxins and lectins are both directly cytotoxic to cancer cells and immune stimulating. The combination of active compounds in mistletoe extract appears to result in a general immune surveillance effect.

Mistletoe therapy assists in breaching the cancer’s microenvironment and damaging cancer cells. Simultaneously, it supports the white blood cells’ ability to identify the tumour as a threat and disburse that information throughout the body.

The goal of mistletoe therapy is to create a” mantle of warmth that envelops the patient”, immune balance and systemic regulation throughout the body to support optimal conditions for remission and healing.

Mistletoe Lectins - Mistletoe lectins are a group of complex proteins that bind to specific cancer cell surface carbohydrate groups. Mistletoe Lectins I, II and III have demonstrated destructive effects on cancer cells, with Lectin III being the most potent and Lectin I being the least.

A fourth unique lectin, chitin-binding agglutinin, in mistletoe appears to interact more with immune cells, heightening their activities.

Mistletoe Viscotoxins - Viscotoxins are plant defensins that plants produce to protect themselves from parasites, bacterial and fungal infections. Human cells also produce some defensins.

Normal, healthy human cells have a positively charged cell surface. The cell surface of rapidly dividing cancer cell has a negatively charged cell surface. Viscotoxins preferentially bind to the negatively charged cancer cell membranes and literally” punches” a hole (pore) into the membrane. This pore allows calcium to flood into the cancer cell resulting in loss of structural integrity and destruction.

In addition, once the pore is wide enough, the viscotoxin itself enters the cell, binding with and further destroying cellular components.

Other Mistletoe Constituents - Other constituents of mistletoe include flavonoids like quercetin (induces apoptosis or programmed/normal cell death), thiol such as glutathione (the body’s master anti-oxidant) and several triterpenes which have been studied for their ability to inhibit metastasis and induce apoptosis.

The most important take-away from the above is the specificity of lectin-binding to cancer cell surface carbohydrates and viscotoxins preference for binding with cancers rapidly-dividing, negatively charged cell surfaces.

Ozone (Oxidative) Therapy

Ozone or energized oxygen is a gas (O3) with a multitude of both industrial and medical uses. Ozone use began is 1871 and there was an increased use during World War II to treat infected wounds.

Ozone use is safer than aspirin when administered by a trained professional, however, inhalation of ozone gas is extremely irritating to the lungs. We administer ozone either intravenously, rectally or topically. The major benefits of ozone are that it increases metabolic efficiency, optimizes immune function and improves circulation. Ozone, like many orthomolecular therapies, has a fundamental action which enables the body to re-balance and heal itself.

If high concentration ozone is injected directly a tumor or other abnormal tissue e.g. an infected or enlarged prostate gland, it will destroy that tissue. This has is called “Ozonolysis Tissue Destruction”.

Direct Intra-venous (DIV) Ozone Administration – DIV ozone detoxifies and super oxygenates the entire blood volume in less than 30-minutes. The blood is saturated with ozone without ever leaving the intra-vascular space.

DIV O3 is used to treat a myriad of diseases and the list is getting longer every day. It may also be the ultimate anti-aging medicine. The following is a list of some of the more common diseases that DIV O3 is used to treat:

1. Cancer
2. Cardiovascular, Stroke and Obstructive Peripheral Vascular Disease
3. Diabetes Mellitus and its complications
4. COVID (both acute and long), HIV, Hepatitis, Herpes Simplex, Lyme Disease and all manner of viruses, bacteria, parasites, yeast and fungus.
5. Chemical sensitivities
6. Macular Degeneration
7. Chronic bladder conditions
8. Inflammatory bowel disease, Crohn’s disease and most forms of colitis
9. Auto-immune disease including, but not limited to, Rheumatoid arthritis, Ankylosing spondylitis, Lupus and others.
10. Eczema and Psoriasis
11. Lipid disorders

Future Medicine will be the Medicine of Frequencies.” - Albert Einstein

Rife Therapy is a non-invasive therapy that works by emitting non-disease-causing radio frequency waves at high power. Each session lasts approximately 20-minutes. These frequencies have been proven to destroy pathogenic viruses, bacteria, fungi, parasites and cancer.

All cells resonate (reverberate or vibrate) at a certain frequency, if this frequency is matched by an external device the potential exists that the external frequency will cause the “shattering” and therefore destruction of the cell or pathogen that it is resonating with. A perfect example is that of a singer whose voice output resonates equally with the resonance of a glass resulting in the shattering of the glass. This is exactly what happens when pathogenic microbes and cancer are exposed to the frequencies of the Rife Machine, they are completely destroyed.

Persons suffering from unexplained medical illnesses should be evaluated for chronic parasitic and fungal infections. Parasite and fungal infections are one of the most neglected areas in medicine (and dentistry). These infections don’t just cause the usually seen symptoms of diarrhea, bloody stool or abdominal cramps but also may be significant contributors to chronic fatigue, headaches, joint pains, fibromyalgia, muscle weakness, autoimmune disease, inflammatory bowel disease, Crohn’s disease, abnormal weight gain, cancer and other diseases.

Parasites can be microscopic protozoal such as Giardia lamblia, Entamoeba histolytica, cryptosporidium or macroscopic/worms such as pinworms, roundworms, tapeworms, hookworms, filarial and others. The usual fungus is candida, although there are others.

A primary cause and/or significant contributor to most illnesses is a dysfunctional immune system. Along with food allergies, poor diet/nutrition, dental problems and heavy metal toxicity, parasitic and fungal infections are cause significant immune dysfunction.

Unfortunately, in addition to most care providers not considering these infections, most laboratories fail to detect these pathogens by conventional tests. This is where bio-energetic testing - BDORT, AMA testing - shows its exceptional ability to detect hidden infections that would otherwise go undetected and untreated.

We live in a beautiful but increasingly toxic world where we are constantly exposed to heavy metals that significantly impair our health. We now know that heavy metals (mercury, arsenic, lead, cadmium, aluminum and others) play a major role in most, if not all chronic degenerative disease.

Though we do not sense heavy metals the usual sense, we are constantly exposed to them through air and water pollution, personal care products, insecticides, medicines and even food. Our bodies have excellent detoxification systems; however, the sheer volume of heavy metal toxins can easily overwhelm our detoxification systems. This leads to storage (and constant exposure) of heavy metals in our lymphatic, circulatory, vital organs and especially fatty tissue.

Even though our bodies can handle very low levels of heavy metals, scientists are discovering that what we previously called “normal ranges” are actually too high. Heavy metals act as poisonous obstructions to our energetic and metabolic systems (creating free radicals, disturbing cell architecture, reducing cell membrane fluidity), and are significant causes of high blood pressure, prostate disease, heart disease, chronic fatigue, brain/cognitive function decline, cancer, pre-mature aging and other chronic degenerative diseases. Therefore, no matter how good our diet, exercise, nutrition and therapeutic interventions, they will not work optimally if we have toxic levels of heavy metals.

Chelating agents (EDTA, DMPS, Chlorella) are usually administered either orally or by rectal suppository, however, can be given intravenously in severe cases. Chelating agents preferentially bind to toxic metals and as the body has no use for the chelating agents, the chelating agent-heavy metal complexes are eliminated by the kidneys.

Chelating agents bring benefits to the entire heart/vascular system, brain and other vital organs and are therefore extremely important for maintaining optimal health.