ALTERED IMMUNITY & THE LEAKY GUT SYNDROME

The leaky gut syndrome is the name given to a very common health disorder in which the basic organic defect (lesion) is an intestinal lining which is more permeable (porous) than normal. The abnormally large spaces present between the cells of the gut wall allow the entry of toxic material into the bloodstream that would, in healthier circumstances, be repelled and eliminated.

The gut becomes leaky in the sense that bacteria, fungi, parasites and their toxins, undigested protein, fat and waste normally not absorbed into the bloodstream in the healthy state, pass through a damaged, hyperpermeable, porous or ÒleakyÓ gut. This can be verified by special gut permeability urine tests, microscopic examination of the lining of the intestinal wall as well as the bloodstream with phase contrast or darkfield microscopy of living whole blood.

Why is The Leaky Gut Syndrome Important?

The leaky gut syndrome is almost always associated with autoimmune disease and reversing autoimmune disease depends on healing the lining of the gastrointestinal tract. Any other treatment is just symptom suppression. An autoimmune disease is defined as one in which the immune system makes antibodies against its own tissues. Diseases in this category include lupus, alopecia areata, rheumatoid arthritis, polymyalgia rheumatica, multiple sclerosis, fibromyalgia, chronic fatigue syndrome, Sjogren's syndrome, vitiligo, thyroiditis, vasculitis, Crohn's disease, ulcerative colitis, urticaria (hives), diabetes and Raynaud's disease. Physicians are increasingly recognizing the importance of the gastrointestinal tract in the development of allergic or autoimmune disease. Understanding the leaky gut phenomenon not only helps us see why allergies and autoimmune diseases develop but also helps us with safe and effective therapies to bring the body back into balance.

Due to the enlarged spaces between the cells of the gut wall, larger than usual protein molecules are absorbed before they have a chance to be completely broken down as occurs when the intestinal lining is intact. The immune system starts making antibodies against these larger molecules because it recognizes them as foreign, invading substances. The immune system starts treating them as if they had to be destroyed. Antibodies are made against these proteins derived from previously harmless foods. Continue reading >>

More informations here:

• Live_blood Analysis
• Live_Blood_Analysis Darkfield Microscopy Courses
• dark field microscopy
• pleomorphism
• Günther Enderlein

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Darkfield Microscopy

FUNGUS
The species specific understanding of, and difference between bacterial phase and fungal phase developments in blood pictures.

©Copyright 1997 by Michael Coyle, Petaluma, California, USA
(Explore Issue: Volume 8, Number 3)

Diseases of the skin, digestive organs, urogenitary tract, mouth, etc. are caused by the multiplication and spread of fungal microorganisms known as mycelia. Mycoses (fungal infections) range in degree from unnoticed to fatal. They are directly related to asthma and allergic alveolitis reactions. They are dealt with by the immune system and competition from other microbes or earlier developmental phases of their own cyclogeny.

Fungal infections can be classified as;

Superficial -- those that effect hair, skin, nostrils, genitals, and oral mucosa

Subcutaneous -- those which occur beneath the skin

Deep -- those which effect the internal organs, lungs, liver, bones, lymph, brain, heart, and urinary tract

These infections often occur in those on long-term antibiotic therapies, corticosteroids, and immunosuppressant drugs. This type of opportunistic infection is common in those with the acquired immunodeficiency syndrome, commonly known as AIDS, and also CFIDS (chronic fatigue syndrome).

Primitive bacterial varlents (thecits)
Some of these fungal forms are received from the environment, are transmitted sexually, or are transmitted through mother's milk (Candida albicans). Candida remains in non-virulent phases of development until the terrain allows for its progression into more complex pathogenic forms. The efficacy of many of the SANUM fungal remedies is based on the sexual activity of the particular species of microorganisms (and/or the benign effect altogether, through competition, on the terrain) which is initiated through the process of reinstalling the microbial flora in the body in it's apathogenic earlier phases of development.

The flora that was installed then copulates with the pathogenic variety and shares the sexual information of the earlier phases, which, all things being equal (terrain modulation, removal of stressors, proper diet, lifestyle, etc.) causes the pathogenic form to convert or be reduced to the apathogenic variety. It is believed that the pathogens are also reduced in valence through the actual activity of the copulatory process.

The main causes of pathogenic albicans overgrowth are indiscriminate antibiotic application and dental inclusions from mercury tooth amalgams. Other factors include addictions to coffee, chocolate, drugs, unsafe sexual pratices, immuncompromisation, stress, chemicals, radiation, improper diet, etc.

The fungal overgrowth occurs because its natural competitors have been removed, in the case of antibiotic usage. In the case of dental amalgams or metals, it is due to decreased immunity from immunocompromisation. The candida also adsorbs the mercury in the gut, thereby serving the function of keeping it from moving deeper in the system, to some degree. A good inclusion in a program of remedies for alleviation of mercury toxicity in the nervous system and brain is broken cell wall chlorella, because not only is it similar to the fungus in that it adsorbs the mercury, but also carries it away. Continue reading >>

FDA Issues New Warnings for Anemia Drugs

(HealthDay News) -- The U.S. Food and Drug Administration on Thursday approved new "black box" warnings on labels of erythropoiesis-stimulating agents, which are drugs used to treat certain types of anemia.

The warnings cover the drugs Aranesp, Epogen and Procrit, and detail their dangers to patients with cancer and patients with chronic kidney failure. Those dangers include heart attack, stroke, heart failure and cancer tumor growth and shortened survival.

The drugs had been touted as a treatment to lessen fatigue and improve quality of life among cancer, HIV and other patients with anemia, but the new label says there's no evidence to back that claim.

"Today's labeling changes are being made to make clear recommendations about the safe and effective use of these products and to strengthen the information about the risks that these drugs pose to patients with cancer and to patients with chromic kidney failure," Dr. Richard Pazdur, the FDA's director of the Office of Oncology Drug Products at the Center for Drug Evaluation and Research, said at a Thursday teleconference.

This is the fifth time the FDA has called for label changes for these drugs -- also known as ESAs -- since Procrit was approved in 1989, Pazdur said.

"We are emphasizing that ESAs should be used at the lowest dose necessary to avoid blood transfusions, since that is the only identifiable benefit for ESAs," Dr. John Jenkins, director of the FDA's Office of New Drugs. "Doctors should have discussions with their patients about whether to use ESAs at all."

These drugs are synthetic versions of a protein made in the kidney that tells bone marrow to produce red blood cells. The drugs are manufactured by Amgen Inc., of Thousand Oaks, Calif. Procrit is marketed and distributed by Ortho Biotech LP of Bridgewater, N.J., a subsidiary of Johnson & Johnson.

Dr. Roger M. Perlmutter, Amgen's executive vice president of research and development, said in a prepared statement that his company "has been working closely with the FDA and J&JPRD [Pharmaceutical Research and Development] to ensure that the information contained in the approved labeling for ESAs accurately reflects the current state of knowledge of these important products and to develop a comprehensive and feasible clinical study program to complement our existing pharmacovigilance program.

"In the current label revisions, we have endeavored to include as much information as possible so physicians and their patients can make informed treatment decisions," he added.

For cancer patients, the new warnings emphasize that the drugs can cause tumor growth and reduce survival among patients with advanced breast, head and neck, lymphoid and non-small cell lung tumors. This is especially true when the dose is designed to produce a hemoglobin level of 12 grams per deciliter of blood or more.

For hemoglobin levels less than 12 grams per deciliter, the label will say there is no evidence to determine if the drugs cause any of these problems, the FDA said.

"We recommend that prescribers talk to their patients about the risks that ESAs might cause cancer to grow or shorten survival before they prescribe these drugs or continue ESA therapy, Pazdur said. "The risks should be weighed against blood transfusions and their associated risks."
The new label will also make it clear that ESAs should be used in cancer patients only when their anemia is caused by chemotherapy and not from other causes. Also, ESAs should be stopped when the patient's chemotherapy has ended, the FDA said.

For patients with chronic kidney failure, the new black box warning says that ESAs should be used to keep hemoglobin levels between 10 grams per deciliter to 12 grams per deciliter. Higher hemoglobin levels in these patients can increase the risk for death, stroke, heart attack or heart failure, the FDA said.

The new labeling also gives instructions for dosage adjustments and hemoglobin monitoring for chronic kidney failure patients who do not respond to ESA treatment.

The new label also says there is no evidence that ESAs improve symptoms of anemia, quality of life, fatigue, or patient well-being in cancer patients or patients with HIV taking the drug AZT.

"There are no data from controlled trials demonstrating that ESAs improve symptoms of anemia, quality of life, fatigue or patient well-being," Pazdur said.

The FDA is working with Amgen on new clinical trails and is also reviewing a Medication Guide that will explain the use of these drugs to patients, Pazdur said.

Epogen, Procrit and Aranesp are used to treat anemia in patients with chronic kidney failure and anemia caused by chemotherapy in some cancer patients. Epogen and Procrit are also used in some anemic patients who are undergoing surgery to reduce the need for blood transfusions. These drugs are also used to treat anemia in HIV patients taking AZT.

More information
For more information on ESAs, visit the U.S. Food and Drug Administration.

Aplastic Anemia: A Rare Disease With a Better Prognosis

(HealthDay News) -- Aplastic anemia, a disease of the bone marrow, is a rare disorder in the United States. Only three of every 1 million Americans will be diagnosed with the condition this year, the National Marrow Donor Program reports.

Despite that rarity, this once-fatal disease has become far more treatable as physicians have honed in on practices that can prolong life and ease suffering.

And the effects of that research extend far beyond sufferers of aplastic anemia or other related bone marrow diseases. Insights gained from these diseases are also helping scientists learn about more prevalent health problems, such as heart disease or leukemia, researchers say.

Aplastic anemia occurs when bone marrow stops producing enough blood cells, said Katherine Baer, a patient information specialist for the Aplastic Anemia and MDS International Foundation Inc. Only about 1,000 new cases appear each year in the United States.

A related blood disorder, myelodysplastic syndromes, or MDS, occurs when the bone marrow begins producing poorly functioning or immature blood cells. About 20,000 to 30,000 new cases occur each year.

Doctors still aren't certain exactly what causes the diseases' onset, Baer said.

"They do think it can be caused; there are some toxins that may cause it, like benzene," Baer said. "But at least half the cases are of unknown cause." She added that radiation treatments for other diseases are another suspected cause.

The effects of aplastic anemia and MDS vary, depending on the type of blood cells lacking in the body, Baer said.

Red blood cells carry oxygen, and a shortage of those will cause fatigue and shortness of breath. White blood cells fight infection, so when the body lacks those cells, it is more likely to catch infectious diseases. Platelets cause clotting, and without those, people experience nosebleeds, bleeding gums and extended bleeding from cuts.

These diseases used to be killers, fatal within a year, said Dr. Richard Stone, clinical director of the Adult Leukemia Program at Harvard University's Dana-Farber Cancer Institute and an associate professor at Harvard Medical School.

"Now, people can be expected to live a long time in many cases," Stone said. "It's devastating if untreated but quite approachable if treated."

Baer and Stone said that while no breakthrough treatments have been developed, the available therapies are at the point where people can live with the disorders.

Most people with aplastic anemia will require multiple blood transfusions, which relieve symptoms by providing blood cells that the bone marrow isn't producing, Baer said. Symptoms also can be managed with immunosuppressive drugs similar to those used in AIDS treatment. The drugs suppress the activity of immune cells that are damaging bone marrow, helping the marrow recover and generate new blood cells, she said.

Antibiotics can be used to effectively fight off infections that take advantage of the disorder. And for a longer-term therapy -- or for people with severe aplastic anemia -- bone marrow transplantation is an option, but a limited one due to the difficulty involved in finding a matching donor.

Experimental treatments now being tested include growth factor drugs that may help stimulate the bone marrow to produce new blood cells; male hormones that also might boost blood cell production; and peripheral stem cell transplants. In that procedure, stem cells are taken from the blood of a donor, rather than from their own bone marrow, and transplanted into the patient, according to the Mayo Clinic.

"Twenty, 30 years ago, it [aplastic anemia] was fatal," Baer said. "Now, between the different treatments, 70 to 90 percent can live a long life. You have to continue to monitor your blood counts, and you are on some medication long-term."

Since these diseases involve damage to stem cells, research in this area could provide much insight into the potential of stem cells for treating other types of diseases. Stem cells have attracted much research focus due to their potential regenerative powers and ability to transform themselves into a host of different cells.

Bone marrow stem cells are the most primitive cells in the marrow, and from them, all the various types of blood cells are descended. Research also has shown that stem cells from bone marrow can give rise to non-marrow cells, which has led to federal funding to look into their usefulness in treating heart disease.

"It's very important to understand as much as possible about the bone marrow stem cell," Stone said. "What keeps it going, what causes it to become malignant? The more we understand about those things, the more we'll know about potential uses of stem cells."

More information
To learn more, visit the Aplastic Anemia and MDS International Foundation Inc.
and: http://www.dreddyclinic.com/findinformation/aa/anemiaaplastic.htm

Fatigue

Fatigue is probably the major symptom or complaint of an overly acidic body.

The toxins produced in an acidic body environment reduce the absorption of protein and minerals, which in turn weakens the body's ability to produce enzymes and hormones.

This also interferes with the reconstruction of cells and other necessary components of energy production.

The result is fatigue, poor endurance, an inability to add muscle tone, and general weakness.

For more information on fatigue go to: phmiracleliving.com or read Sick and Tired by Dr. Robert O. Young

Dr. Robert O. Young's New Biology, most simply stated, is that the over-acidification of the body is the single underlying cause of all disease.

Dr. Robert O. Young's New Biology, most simply stated, is that the over-acidification of the body is the single underlying cause of all disease.

In contrast, the old biology, based on the work of Louis Pasteur in the late 1800s, stems from the idea that disease comes from germs which invade the body from the outside. Dr. Young has found that when the body is in healthy alkaline balance, germs are unable to get a foothold.

Think of your body as a fish tank. Think of the importance of maintaining the integrity of the internal fluids of the body that we "swim" in daily. Imagine the fish in this tank are your cells and organ systems bathed in fluids, which transport food and remove wastes.

Now imagine we back up a car and put the tailpipe up against the air intake filter that supplies the oxygen for the water in the tank. The water becomes filled with carbon monoxide, lowering the alkaline pH, creating an acidic pH environment, and threatening the health of the "fish," your cells and organs.

What if we throw in too much food or the wrong kind of food (acid-producing food like dairy, sugar, and animal protein) and the fish are unable to consume or digest it all, and it starts to decompose and putrefy?

Toxic acid waste and chemicals build up as the food breaks down, creating more acidic byproducts, altering the optimum alkaline pH.

Basically, this is a small example of what we may be doing to our internal fluids every day. We are fouling them with pollution, smoking, drugs, excessive intake of food, over-consumption of acid-forming foods, and any number of transgressions which compromise the delicate balance of our internal alkaline fluids.

Some of us have fish tanks (bodies) that are barely able to support life, yet we somehow manage to struggle from day to day, building more severe imbalances until there is the inevitable crash and debilitating chronic, disturbing and disorganizing symptoms to deal with.

The pH level (the acid-alkaline measurement) of our internal fluids affects every cell in our bodies. Extended acid imbalances of any kind are not well tolerated by the body. Indeed, the entire metabolic process depends on a balanced internal alkaline environment.

A chronically over-acidic pH corrodes body tissue, slowly eating into the 60,000 miles of veins and arteries like acid eating into marble. If left unchecked, it will interrupt all cellular activities and functions, from the beating of your heart to the neural firing of your brain. In summary, over-acidification interferes with life itself leading to all sickness and disease!

How do you know if you're overly acidic?

Fat is an Acid Problem!

Perhaps one of Dr. Young's most well known discoveries is his theory of the cause of overweight. He has shown that fat is actually an over-acidification problem. What does that mean?

The body creates fat cells to carry acids away from your vital organs, so these acids literally don't choke your organs to death. Fat is saving your life! Fat is actually a response from the body to an alarming over-acidic condition.

What about Underweight?

At the other end of the health spectrum, the yeast and fungus produced within an overly acidic body can feed on your nutrients and reduce the chemical and mechanical absorption of everything you eat by as much as 50%.

This causes many people to become excessively thin, which is no healthier than becoming overweight. Without protein, your body cannot rebuild new tissues or produce enzymes, hormones, or hundreds of other chemical components necessary for cell energy and organ activity. Fatigue, illness, and body weight changes are the results.

An underweight person may loose a little more weight as their body chemistry stabilizes. As their body normalizes, they will begin to gain towards their ideal weight.

Healthy bodies are not overweight or underweight. A healthy body naturally maintains its own ideal weight. As alkalizing and oxygenation begins to take place, the body naturally begins to seek its own ideal weight.

For more information on weight gain or weight loss go to: http://www.phmiracleliving.com/audios.htm or read the pH Miracle for Weight Loss

Related Courses
· Live Blood Analysis (3 days)
· Live Blood Analysis (6 days)
· Live Blood Analysis (80 hours)
· Live Blood Analysis online course (1year)
· Colon Hydrotherapy Course 45 hours (6 Days)
· Cleansing Combo Pack
· Microscope Equipment

The Pacelli Chiropractic & Health Potential Complex Web site states:

How often do you get to see if small changes in nutrition, really can make a difference?

Well in this case, that's how we work. After making our recommendations, we repeat the test in 2 weeks, and look to see if we see changes.

This way you get to see the changes in your blood as we help correct the problems, it also allows us to check dosages to make sure that you are getting the proper amount of the vitamin, mineral, protein, or enzyme you need to restore you to optimal health.

These claims are sheer bunkum. Dark-field microscopy is a valid scientific tool in which special lighting is used to examine specimens of cells and tissues. The objects being viewed stand out against a dark background-the opposite of what occurs during regular microscopy.

This allows the observer to see things that might not be visible with standard lighting. Connecting a television monitor to a microscope for diagnostic purposes is also a legitimate practice. However, live cell analysis is not. Although a few characteristics of blood (such as the relative size of the red cells) are observable, live cell analysts invariably misinterpret other things, such as the extent of red blood cell clumping, changes in the shape of the cells, and other artifacts that occur as the blood sample dries.

Moreover, most practitioners who perform the test are not qualified to manage the problems they purport to diagnose.

During the mid-1980s, one company marketing live-cell equipment projected that a practitioner who persuades one patient per day to embrace a supplement program based on the test would net over $60,000 per year for testing and supplement sales. Another company estimated that with five new patients a day (22 days a month) paying $30 for the test and $50 for supplements, practitioners would gross over $100,000 per year just on initial visits.

Today's most active individual promoter of live-cell analysis is probably James R. Privitera, M.D., of Covina, California, who claims that "clot malfunction" is an underlying cause of many diseases, can be diagnosed with live cell analysis, and can be treated with large doses of dietary supplements.

His book, Silent Clots, describes his "general daily guidelines [for supplements] that have worked well for many patients as an anti-clotting program." The book also describes regimens for arthritis, asthma, baldness, bladder infections, cancer, colds, colitis, cramps, diabetes, diarrhea, diverticulosis, eczema, and edema, and includes case histories of patients he treated for many other conditions [1].

I do not believe there is any scientific evidence for these claims or that these regimens are effective as Privitera claims. His's web site offers more than 150 supplement products for sale.

In 1975, Privitera was convicted of conspiring to prescribe and distribute laetrile and was sentenced to six months in prison. (Laetrile is a quack cancer remedy.) In 1980, after the appeals process ended, he served 55 days in jail but was released after being pardoned by California Governor Jerry Brown. (The pardon occurred in response to a letter-writing campaign generated by the National Health Federation, a group that espouses what it calls "health freedom.")

Then, because Privitera had been prescribing unapproved substances (including laetrile, calcium pangamate, and DMSO) for the treatment of cancer, the California Board of Medical Quality Assurance suspended his medical license for four months and placed him on ten years' probation under board supervision.

During the probationary period, Privitera was "prohibited from making any representation that he is able to cure cancer through nutrition." He was also forbidden to tell patients they had cancer unless the diagnosis was confirmed in writing by an appropriate board-certified specialist.

During the probationary period, Privitera commercialized live-cell analysis and founded two companies that marketed devices for doing it. Silent Clots mentions that in 1993, a federal judge signed an order authorizing Internal Revenue Service agents to enter his clinic premises to effect a levy and that a seizure was made.

However, the book provides no further details about his tax-related difficulty.

Critical Reports
During the mid-1980s, National Council Against Health Fraud vice president James Lowell, Ph.D., watched three practitioners demonstrate live cell analysis at health expositions.

Lowell noted:
None took precautions during the preparation of the slides to prevent the blood from drying out or clotting.

They failed to clean their microscope slides carefully between patients, which meant that dirt seen under the microscope would be misinterpreted as blood components.

Some of the patterns one practitioner saw resulted from his microscope being out of focus and disappeared when Lowell adjusted it properly. [2}

Live cell analysis is also promoted by Infinity
2, of Scottsdale, Arizona, a multilevel company whose distributors often demonstrate their wares at chiropractic conventions. Infinity2 calls the test "live cell microscopy" and recruits licensed health professionals to use the procedure to sell its products. In 1995, I was tested at a national chiropractic convention where two teams of Infinity distributors had exhibits.

One exhibitor said I had "mild B12 deficiency" and "maldigestion" that could weaken my immune system and cause fatigue. The other said my blood cells showed evidence of "liver toxicity," "bacterial infection," and "free radical damage."

In both cases the recommended "treatment" was enzyme pills, which the company was marketing with false claims that "enzyme deficiency" is widespread among Americans. To reinforce their that the pills could help me, both practitioners gave me enzyme pills, repeated the procedure several minutes later, and said that the problems were no longer visible. Unknown to them, however,

I had faked taking the pills, so the "improvements" they saw had nothing to do with them. The most likely explanation is that the specimens were examined differently. Blood dries more quickly near the edges of the slide than near the center. Thus "improvement" will occur if the first specimen is examined near an edge and the second specimen is examined near its center.

Legal Action
In 1996, the Pennsylvania Department of Laboratories informed three Pennsylvania chiropractors that Infinity2's "Nutritional Blood Analysis" could not be used for diagnostic purposes unless they maintain a laboratory that has both state and federal certification for complex testing [3].

The company's attorney replied:
As background, you should know that part of our business activity is supplying a microscope system that is equipped for the demonstration of blood samples on a video monitor. We teach and recommend the use of this system as a health education demonstration. In our training and system we do not teach, promote or address in any manner using the system for "analysis" or any other medical purpose.

Our system is based on obtaining a written nutritional and lifestyle analysis from patients of doctors using the microscopy system. Once this questionnaire and evaluation of lifestyle and nutrition is examined by the doctor, the doctor then makes specific recommendations to the patient, based solely and exclusively on the nutritional analysis and personal interview with the patient.

After any recommendation has been made for altering the patient's lifestyle or nutritional habits, the doctor may place a single drop of blood on a sample slide for viewing through the dark field microscope which is then displayed on a video monitor.

This demonstration is a powerful motivating tool to encourage a doctor's patient to accept the doctor's previously made recommendations and alter his or her lifestyle to a healthier form of living.

The doctor performing the demonstration never makes any analysis, determination or recommendation based on the video demonstration. There is no commentary given regarding the state of the patient's blood or anything seen in the bloodscreen itself other than to educate the patient by pointing out features of the blood such as red cells, white cells, and plasma. The patient is able to view a sample of his/her own blood, which results in the motivation that can lead to beneficial lifestyle changes for the individual patient [4].

A Laboratory Department official then informed the attorney that certification would be required if the practitioner:

Either prescribed a nutritional supplement or changed the amount or type of a supplement based on viewing a blood sample.

Recommended lifestyle or nutritional changes based on viewing a blood sample.
Performed nutritional microscopy more than once for a given patients.

Compared the patient's blood smear to that of another slide or picture
Showed the patient's blood smear and making any comment or providing any information other than to point out features of the blood such as red cells, white cells, and platelets [5].

Very few if any chiropractors would have reason to seek laboratory certification, and even if they did, I doubt that permission would be granted to perform this test for diagnostic purposes. If you encounter anyone who performs any type of live cell analysis, please report this to your state department of laboratories and send a copy of your notice to me at P.O. Box 1646, Allentown, PA 18105

Reference
1. Privitera J, Stang A. Silent Clots: Life's Biggest Killers. Lockstep Medicine's Conspiracy to Suppress the Test That Should Be Done in Emergency Rooms Throughout The World. Covina, Calif.: The Catacombs Press, 1996.
2. Lowell JA. Live cell analysis: High-tech hokum. Nutrition Forum 3:81-85, 1986.
3. Wlazelek A. Chiropractors cease blood cell show and tell. State restricts the use of magnified images to sell vitamins, supplements. The Morning Call, April 12, 1996, page B6.
4. Woodruff SM. Letter to Joseph W. Gasiewski, Director, Division of Laboratory Improvement, Pennsylvania Department of Health, Jan 17, 1996.
5. Gasiewski JW. Letter to Samuel M. Woodruff, General Counsel, Infinity2, Feb 16, 1996.
Chirobase

Detoxamin EDTA Chelation Therapy, Time Release Calcium Disodium EDTA

Detoxamin EDTA Chelation Therapy Suppositories are a new patented method of Ca-EDTA chelation therapy medically equivalent to I.V. chelation therapy. The difference is that Detoxamin introduces a smaller dosage of Calcium Disodium EDTA on a nightly basis.
order here:

By applying the highly efficacious Detoxamin suppository containing EDTA, you remove toxic metal from cells all over the body. The self-administration is performed rectally before retiring so that as you sleep you are taking chelation therapy with EDTA. There's no need for intravenous infusions or quantities of nutritional supplements.

What is EDTA chelation therapy and what is it used for?
Chelation (pronounced key-lay-shun) is the process by which a metal or mineral (such as lead, mercury, iron, arsenic, aluminum, etc.) is bonded to another substance-in this case an amino acid called EDTA, Ethylene-Diamine-Tetra-Acetic acid. It is a natural process, basic to life itself.

During EDTA chelation therapy, the EDTA infusion bonds with unwanted metals in the body and quickly carries them away in the urine. Chelation therapy is a safe, effective alternative to drugs and surgeries and is used to treat many illnesses now known to be linked to the presence of toxic heavy metals.

Illnesses such as heart disease, strokes, diabetes, circulatory disorders, neuropathies, Alzheimer's disease, atherosclerosis, and adverse reactions to many environmental pollutants. Traditional chelation therapy uses an intravenous drip, and is administered in the outpatient setting. The number of treatments vary based on each person's individual condition and/or goals of treatment. The average therapy is given one to three times a week for twenty to thirty treatments.

How long has EDTA chelation therapy been in use? Why don't more people use it?
EDTA chelation therapy for the detoxification for heavy metals has been in continuous use since the 1940s when it was introduced specifically for the treatment of lead poisoning. It was very quickly observed that as the metals were eliminated, not only did the signs and symptoms of lead poisoning abate, but problems related to the circulatory system like heart attacks, angina, strokes, and peripheral vascular disease also improved. For the past 50 years, well over one million people have received the intravenous form of EDTA chelation. As beneficial and life saving as this therapy has become, it is very expensive and very time-consuming, making it out of reach for most people.

Why is Ca-EDTA, Calcium Disodium EDTA, so much better than other types of chelation therapy?
According to Dr. Bruce Halstead, "The chemistry of all chelators is such that a change of pH can dramatically effect the process of chemical binding needed to chelate a mineral or metal. When you use a less effective chelator, such as Magnesium EDTA, you lose all chelating ability of the two most essential heavy metals: lead and mercury. Magnesium di-Potassium EDTA has a dramatically lower chelating effectiveness than Calcium EDTA because both magnesium and potassium dramatically decrease the pH in the blood environment to which it is introduced. Any factor decreasing pH renders EDTA less effective. Once the pH is lowered more than 7.38, it's no longer chemically conducive to any bonding or chelating." (Dr. Halstead is well known as the 'Father of Chelation Therapy'.)

Dr. Morton Walker Speaks on Detoxamin - Toxic Metals Induce Degenerative Diseases; Rectal Chelation Therapy Overcomes Them.

Environmentalists warn us repeatedly that we live on a poisoned planet. Toxins from mercury, lead, aluminum, cadmium, iron, nickel, and about 20 more metallic minerals permeate the Earth's milieu. Heavy and light metals poison us by combining to create deleterious signs and symptoms often referred to collectively as Toxic Metal Syndrome.

This syndrome, an indicator of serious systemic pathology, results in degenerative diseases which affect no less than 92% of the populations of Western industrialized nations, in particular, those people living in apartment high-rises and other polluted city dwellings. What happens to them? These poisoned people eventually come down with manifestations of degenerative illnesses such as heart and/or blood vessel deteriorations; pancreatitis; gout, rheumatoid arthritis or osteoarthritis; the syndromes of yeast, chronic fatigue, and/or irritable bowel; Alzheimer's disease, multiple sclerosis, parkinsonism, and many more which may be deadly-cancer for instance.

Although a poisoned person's bones remain toxic for life, excellent self-treatment exists to reduce or reverse most symptoms of illness in other body parts. First, get tested for the extent of toxicity, then neutralize metallic poisoning with a chelating agent such as Detoxamin. By applying the highly efficacious Detoxamin suppository containing EDTA, you remove toxic metal from cells all over the body. The self-administration is performed rectally before retiring so that as you sleep you are taking chelation therapy with EDTA. There's no need for intravenous infusions or quantities of nutritional supplements.

Rectal chelation therapy does the job of detoxifying in a low-cost, convenient manner; it's an effective way to effuse EDTA through the bowel's walls and into your blood stream to clean toxic metals from all body cells.

Do I need Ca-EDTA chelation therapy?
We find ourselves existing in a far more toxic and hostile environment than our bodies were designed to handle. Experts have shown that almost every health problem-from learning disorders to cancer and heart disease-is aggravated by the approximate 1,000% increase in lead levels in our bones. In 1999, it was reliably reported that hearts with some form of disease have 20,000 times more toxic heavy metals than healthy hearts.

"Human exposure to heavy metals has risen dramatically in the last 50 years as a result of an exponential increase in the use of heavy metals in industrial processes and products." says Maile Pouls, Ph.D (Townsend Letter for Doctors and Patients, July 1999).

A recently concluded "Body Burden" study by New York's Mt. Sinai Hospital and the Environmental Working Group was reviewed by University of Oregon Professor Joseph Thornton: "It shows the universality of chemical contamination of people's bodies," Thornton said. All the studies "confirm the general message that everybody in our society has these chemicals building up. Some people have it worse than others, but everyone has it. No one is clean anymore." (From Being Careful Can't Keep Chemicals Out of Your Body, Miami Herald, February 1, 2003.)

Today we know that about one out of every 2.5 Americans will get cancer. Ninety eight percent of cancer is caused by toxic chemicals. When 50% of all men and 33% of all women living now will die of cancer, something is terribly wrong. (Mortality from cancer was reduced by 90% during an 18-year study of 59 patients treated with Calcium-EDTA. This and over 40 other studies prove the efficacy of Ca-EDTA, Calcium Disodium EDTA chelation therapy and Detoxamin. We will all function better and live longer if we lower the overall burden of toxic metals within ourselves. If you eat or breathe, you will probably benefit greatly from chelation therapy.

Is Detoxamin safe for children?
Yes. In fact, Detoxamin case studies were conducted on lead poisoning in children. The study showed no significant increase in BUN or creatinine levels even in very young children. Due to our lower dosage and time release formulation, no renal toxicity was encountered.

BEHAVIORAL, STRUCTURAL, FUNCTIONAL ABNORMALITIES ASSOCIATED WITH VARIOUS HEAVY METAL TOXINS.

Reference: Published in the August issue of Alternative & Complimentary Therapies (a magazine for doctors) and Published in Townsend Letter for Doctor's and Patients
Psychiatric Disturbances:

Social Deficits, Social withdrawal

Mercury
Repetitive, perseverative, stereotyped behaviors; OCD-typical behaviors

Mercury
Depression, mood swings, flat affect; impaired facial recognition

Arsenic, Copper, Lead, Mercury
Schizoid tendencies; hallucinations; delirium

Mercury
Irritability, aggressive behaviors, temper tantrums

Lead, Mercury
Suicidal Behaviors

Copper, Mercury
Sleep difficulties / disturbances

Lead, Mercury, Thallium
Chronic fatigue (CFS); weakness, malaise

Aluminum, Arsenic, Cadmium, Copper, Lead, Mercury, Thallium
Anorexia; symptoms reflecting eating disorders, loss of appetite/weight

Arsenic, Lead, Mercury
Anxiety; nervous tendencies

Thallium
Attentional problems (ADHD), lacks eye contact, impaired visual fixation

Lead, Mercury
Speech and Language Deficits:
Speech disorders

Aluminum, Mercury
Loss of speech, developmental problems with language

Mercury
Speech comprehension deficitsMercury
Dysarthria; articulation problems; slurred speech, unintelligible speech

Mercury
Cognitive Impairments:
Mental retardation, borderline intelligenceArsenic, Lead, Mercury
Uneven performance on IQ scores, low IQ scores

Copper, Lead
Poor concentration, attention deficits (ADHD, response inhibitionAluminum, Lead
Poor memory (short term, verbal, and auditory)

Aluminum, Lead
Difficulties understanding abstract ideas; difficulty carrying out complex commandsX metals
Dementia; pre-senile and senile dementia

Aluminum
StuporAluminum, Arsenic
Impaired reaction time; lower performance on timed testsLead
Sensory Abnormalities:
Abnormal Sensations in the mouth and extremities

Arsenic
Hearing loss, difficulty hearingArsenic, Lead, Mercury
Abnormal touch sensations; diminished touch sensations, aversion to touch

Arsenic
Blurred vision; sensitivity to lightArsenic, Mercury
Motor Disorders:
Choreiform movements, myoclonal jerks, unusualposturesCopper, Mercury
Difficulty walking, swallowing, talkingCopper, Mercury
Flapping, circling, rocking, toe walking

Mercury
Problems with intentional movements or imitation

Mercury
Abnormal, gait/posture; incoordination, loss of balance; problems sitting, lying, crawling and walkingMercury
Decreased locomotor activity

Aluminum, Arsenic
Convulsion; seizure

Aluminum, Arsenic, Copper, Lead, Mercury, Thallium
Physiological Impairment, Brain and Central Nervous System:
Neurofibrillary tangles

Aluminum
Neuritis, retrobulbar neuritis; neuropathy

Aluminum, Arsenic, Lead, Thallium
EncephalopathyAluminum, Arsenic, Lead, Thallium
Cerebrovascular diseaseX metals
Alterations in nerve conduction velocityLead
Alterations in the spinal cordThallium
Accumulates in CNS structures

Aluminum, Mercury
Abnormal EEGsArsenic, Lead
Autonomic disturbancesCopper, Lead, Mercury, Thallium
Peripheral Nervous System:
Peripheral neuropathyArsenic, Mercury
Alterations in peripheral nervesArsenic
Loss of feeling/ numbness in the extremities; paresthesiaArsenic, Mercury, Thallium
Gastrointestinal Tract:
Nausea, vomiting, diarrhea; loss of appetiteArsenic, Mercury
Abdominal pain, stomach cramps; burning of the throat of the mouthArsenic, Copper, Lead, Mercury, Thallium
Esophagitis; gastroenteritis; colitisArsenic, Mercury, Thallium Cancers (colon, pancreatic, stomach, or rectal) Arsenic
Renal and Hepatic Impairment:
Hepatotoxicity; Liver dysfunction, damageArsenic, Copper, Thallium
Cirrhosis of the liver; hepatitisCopper
Kidney disease; kidney failureArsenic, Lead, Mercury
Renal toxicity; tubular proteinosisArsenic, Copper, Lead
Kidney Damage, histological alterationsArsenic, Lead
Cardiovascular System:
Blood vessel damageArsenic
Anemia; decreased red blood cell countArsenic, Copper
Hypertension; increased heart rate (tachycardia)Arsenic, Copper, Lead, Thallium
Electrocardiac disorders, Peripheral vascular disease; cardiovascular disease, vascular collapseArsenic, Lead
Respiratory System:
Pulmonary FibrosisAluminum, Arsenic
Pulmonary edemaX metals
Pneumonia, laryngitis, pharyngitis, bronchitisAluminum, Arsenic, Mercury
Restrictive airway disorders, asthmatic conditions, pneumoconiosisArsenic, Aluminum
Nasal ulcers, perforation of the nasal septumX metals
Immune System:
Increased incidences of asthma, autoimmune-like symptoms, & allergiesX metals
Inhibition of lymphocytes, T-cells, monocytes X metals
ImmunosuppressionLead
Decreased white blood cell countArsenic, Thallium

Reproductive System:
Genital abnormalitiesAluminum, Thallium
Disturbances in menstrual cycle; menstrual pains

Copper, Mercury
Birth defects; premature births; Spontaneous abortion

Arsenic, Lead, Mercury
Reproductive dysfunction

Arsenic, Aluminum

Other Physical Disturbances:
Hypotonia or hypertonia; decreased muscular strength

X metal
Rashes, contact dermatitis; eczema, itchy/irritating skinAluminum, Arsenic, Copper, Mercury
Muscle pain; headache; acrodynia; colic

Arsenic, Copper, Lead, Thallium
Alopecia (hair loss)

Thallium Reference: Published in the August issue of Alternative & Complimentary Therapies (a magazine for doctors) and Published in Townsend Letter for Doctor's and Patients.

Detoxamin Usage Instructions: Detoxamin EDTA Suppositories are solid, bullet-shaped preparations designed for easy insertion into the anus (back passage). Detoxamin is manufactured in a cocoa-butter base, a time-release agent (fatty acid base), and 750 mg of Calcium-Disodium EDTA. Detoxamin will dissolve at body temperature and will gradually spread over the lining of the lower bowel (rectum), where it is absorbed into the bloodstream. Detoxamin is designed to release 750 mg Calcium Disodium EDTA slowly, over an 80-minute period.

A. Detoxamin Protocol for More Severe Cases:
1. Take one suppository at night, prior to bedtime.
2. Take every night for up to 90 days. This will provide the medical equivalence of 30 IV Chelation treatments.
3. Take proper mineral/trace mineral/vitamin replacement every day.
4. Take all other suplementaion every day.
B. Detoxamin Protocol for Less Severe Cases/Anti-Aging/Prevention:
1. Take Detoxamin every OTHER night, prior to bedtime.
2. Take Detoxamin every other night for 180 days (90 suppositories). This will provide the medical equivalence of 30 IV chelation treatments.
3. Take proper mineral/trace mineral/vitamin replacement every day.
4. Take all other supplementation every day.
Detoxamin Protocol AFTER A or B is completed:
Your bones are toxic for life. Lead and other heavy metals are stored in the bones and get re-distributed into the bloodstream. Therefore, it is highly recommended to continue maintenance with Detoxamin, this provides the ultimate in Anti-aging benefits.
1. Take 5 Detoxamin suppositories over a 30-day period. This porvides medically equal to about 2 EDTA IV treatments.
2. Take porper mineral/trace mineral/vitamin replacement every day.
Note: Detoxamin is designed to be taken at night, however some patients and physicians prefer taking a suppository in the morning after evacuation. (Optional)
How to Use Detoxamin:
Insert Detoxamin suppositories at night, prior to bedtime.
Eat early in the evening, about 4 hours prior to bedtime. (Reduces any discomfort).1. Go to the toilet and empty your bowels if necessary.
2. Wash your hands.
3. Remove the plastic wrapping from Detoxamin.
4. Either squat or lie on your side with one leg bent and the other staight.
5. Gently but firmly push the suppository into the rectum, FLAT end first until past the sphincter muscle. By inserting the flat end first opposed to the pointed end, the suppository will travel higher up in the rectum more easily. If necessarey moisten the suppository with a little water. Push it in far enough so it doesn't slip out.
6. Close your legs and sit or lay still for a few minutes.
7. Wash your hands again.
8. Try not to empty your bowels for at least 80 minutes.
9. It is optional to take Detoxamin in the morning, after evacuation.

STORAGE: Store Detoxamin in a cool dark place, but not in the fridge. If Detoxamin suppository gets warm it may melt, put the fridge for a few minutes, this will return the suppository to its original state so it may be inserted.
Shelf Life: 2 Years

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Heavy Metals Sources and Effects

Heavy Metals - Sources and Effects
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ALUMINUM
Alum, aluminum foil, animal feed, antacids, aspirin, auto exhaust, baking powder, beer, bleached flour, cans, ceramics, cheese, cigarette filters, color additives, construction materials, cookware, cosmetics, dental amalgams, deodorants, drinking water, drying agents, dust, insulated wiring, medicinal compounds, milk products, nasal spray, pesticides, pollution, salt, tap water, tobacco smoke, toothpaste, treated water, vanilla powder.

ALS, Alzheimer's, anemia, appetite loss, behavioral problems, cavities, colds, colitis, confusion, constipation, dementia, dry mouth, dry skin, energy loss, excessive perspiration, flatulence, headaches, heartburn, hyperactivity, inhibition of enzyme systems, kidney dysfunction, lowered immune function, learning disabilities, leg twitching, liver dysfunction, memory loss, neuromuscular disorders, numbness, osteoporosis, paralysis, Parkinson's disease, peptic ulcer, psychosis, reduced intestinal activity, senility, skin problems, spleen pain, stomach pain, weak and aching muscles

ARSENIC
Burning of arsenate treated building materials, coal combustion, insect sprays, pesticides, soils (arsenic rich), seafood from coastal waters, especially muscles, oysters and shrimp

Abdominal pain, anorexia, brittle nails, diarrhea, nausea, vomiting, chronic anemia, burning in mouth / esophagus / stomach / bowel, confusion, convulsions, dermatitis, drowsiness, enzyme inhibition, garlicky odor to breath / stool, hair loss, headaches, hyper-pigmentation of nails and skin, increased risk of liver / lung / skin cancers, low grade fever, mucous in nose and throat, muscle aches / spasms / weakness, nervousness, respiratory tract infection, swallowing difficulty, sweet metallic taste, throat constriction

CADMIUM
Airborne industrial contaminants, batteries, candy, ceramics, cigarette smoke, colas, congenital intoxication, copper refineries, copper alloys, dental alloys, drinking water, electroplating, fertilizers, food from contaminated soil, fungicides, incineration of tires / rubber / plastic, instant coffee, iron roofs, kidney, liver, marijuana, processed meat, evaporated milk, motor oil, oysters, paint, pesticides, galvanized pipes, processed foods, refined grains / flours cereals, rubber, rubber carpet backing, seafoods (cod, haddock, oyster, tuna), sewage, silver polish, smelters, soft water, solders (including in food cans), tobacco, vending machine soft drinks, tools, vapor lamps, water (city, softened, well), welding metal

Alcoholism, alopecia, anemia, arthritis (osteo and rheumatoid), bone disease, bone pain in middle of bones, cancer, cardiovascular disease, cavities, cerebral hemorrhage, cirrhosis, diabetes, digestive disturbances, emphysema, enlarged heart, flu-like symptoms, growth impairment, headaches, high cholesterol, hyperkinetic behavior, hypertension, hypoglycemia, impotence, inflammation, infertility, kidney disease, learning disorders, liver damage, lung disease, migraines, nerve cell damage, osteoporosis, prostate dysfunction, reproductive disorders, schizophrenia, stroke.

COPPER
Birth control pills, congenital intoxication, copper cookware, copper IUDs, copper pipes, dental alloys, fungicides, ice makers, industrial emissions, insecticides, swimming pools, water (city / well), welding, avocado, beer, bluefish, bone meal, chocolate, corn oil, crabs, gelatin, grains, lamb, liver, lobster, margarine, milk, mushrooms, nuts, organ meats, oysters, perch, seeds, shellfish, soybeans, tofu, wheat germ, yeast

Acne, adrenal insufficiency, allergies, alopecia, anemia, anorexia, anxiety, arthritis (osteo & rheumatoid), autism, cancer, chills, cystic fibrosis, depression, diabetes, digestive disorders, dry mouth, estrogen dominance, fatigue, fears, fractures, fungus, heart attack, high blood pressure, high cholesterol, Hodgkin's disease, hyperactivity, hypertension, hyperthyroid, hypoglycemia, infections, inflammation, insomnia, kidney disorders, libido decreased, lymphoma, mental illness, migraines, mood swings, multiple sclerosis, myocardial infarction, nausea, nervousness, osteoporosis, panic attacks, paranoia, phobias, PMS, schizophrenia, senility, sexual dysfunction, spacey feeling, stuttering, stroke, tooth decay, toxemia of pregnancy, urinary tract infections, yeast infections

IRON
Drinking water, iron cookware, iron pipes, welding,. foods: blackstrap molasses, bone meal, bran, chives, clams, heart, kidney, leafy vegetables, legumes, liver, meat, molasses, nuts, organ meats, oysters, parsley, red wine, refined foods, shellfish, soybeans, wheat germ, whole grains

Amenorrhea, anger, rheumatoid arthritis, birth defects, bleeding gums, cancer, constipation, diabetes, dizziness, emotional problems, fatigue, headache, heart damage, heart failure, hepatitis, high blood pressure, hostility, hyperactivity, infections, insomnia, irritability, joint pain, liver disease, loss of weight, mental problems, metallic taste in mouth, myasthenia gravis, nausea, pancreas damage, Parkinson's disease, premature aging, schizophrenia, scurvy, shortness of breath, stubborness

LEAD
Ash, auto exhaust, battery manufacturing, bone meal, canned fruit and juice, car batteries, cigarette smoke, coal combustion, colored inks, congenital intoxication, cosmetics, eating utensils, electroplating, household dust, glass production, hair dyes, industrial emissions, lead pipes, lead-glazed earthenware pottery, liver, mascara, metal polish, milk, newsprint, organ meats, paint, pencils, pesticides, produce near roads, putty, rain water, pvc containers, refineries, smelters, snow, tin cans with lead solder sealing (such as juices, vegetables), tobacco, toothpaste, toys, water (city / well), wine

Abdominal pain, adrenal insufficiency, allergies, anemia, anorexia, anxiety, arthritis (rheumatoid and osteo), attention deficit disorder, autism, back pain, behavioral disorders, blindness, cardiovascular disease, cartilage destruction, coordination loss, concentration loss, constipation, convulsions, deafness, depression, dyslexia, emotional instability, encephalitis, epilepsy, fatigue, gout, hallucinations, headaches, hostility, hyperactivity, hypertension, hypothyroid, impotence, immune suppression, decreased IQ, indigestion, infertility, insomnia, irritability, joint pain, kidney disorders, learning disability, liver dysfunction, loss of will, memory loss (long term), menstrual problems, mood swings, muscle aches, muscle weakness, muscular dystrophy, multiple sclerosis, myelopathy (spinal cord pathology), nausea, nephritis, nightmares, numbness, Parkinson's disease, peripheral neuropathies, psychosis, psychomotor dysfunction, pyorrhea, renal dysfunction, restlessness, retardation, schizophrenia, seizures, sterility, stillbirths, sudden infant death syndrome, tingling, tooth decay, vertigo

MERCURY
Adhesives, air conditioner filters, algaecides, antiseptics, battery manufacturing, body powders, broken thermometers, burning newspapers and building materials, calomel lotions, cereals, congenital intoxication, cosmetics, dental amalgams, diuretics, fabric softeners, felt, floor waxes, fungicides, germicides, grains, industrial waste, insecticides, laxatives, lumber, manufacture of paper and chlorine, medications, mercurochrome, paints, paper products, pesticides, photoengraving, polluted water, Preparation H, psoriasis ointment, seafoods (especially tuna and swordfish), sewage disposal, skin lightening creams, soft contact lens solution, suppositories, tanning leather, tatooing, water (contaminated), wood preservatives

Adrenal dysfunction, allergy, alopecia, anorexia, anxiety, birth defects, blushing, brain damage, cataracts, cerebral palsy, poor coordination / jerky movements, deafness, depression, dermatitis, discouragement, dizziness, drowsiness, eczema, emotional disturbances, excess saliva, fatigue, gum bleeding and soreness, headaches (band type), hearing loss, hyperactivity, hypothyroidism, forgetfulness, immune dysfunction, insomnia, irritability, joint pain, kidney damage, loss of self-control, memory loss, mental retardation, metallic taste, migraines, nervousness, nerve fiber degeneration, numbness, pain in limbs, rashes, retinitis, schizophrenia, shyness, speech disorders, suicidal tendencies, tingling, tremors (eyelids, lips, tongue, fingers, extremities), vision loss.

NICKEL
Butter, fertilizers, food processing, fuel oil combustion, hydrogenated fats and oils, imitation whipped cream, industrial waste, kelp, margarine, oysters, stainless steel cookware, tea, tobacco smoke

Anorexia, kidney dysfunction, apathy, disruption of hormones, fever, hemorrhages, headache, heart attack, intestinal cancer, muscle tremors, nausea, oral cancer, skin problems, vomiting
©2006 World Health Products, LLC

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Detoxamin in the Media

An EDTA Chelation therapy medical breakthrough…"Detoxamin will revolutionize medicine." - Sherry Rogers M.D.
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For years EDTA chelation therapy has been instrumental in literally saving the lives of people across the globe. The results of this therapy have given patients a new lease on life. EDTA chelation therapy works by removing the toxic heavy metals from damaged hearts and heart valves as well as from hidden stores within blood vessels, kidneys, and more. You see, by removing the circulatory heavy metal toxins, EDTA enhances cardiovascular blood flow and function.

As highly recommended as this therapy has been in the past, the only effective way to receive the therapy has been intravenously. This requires sitting in a doctor's office while the EDTA is slowly introduced into your bloodstream, via IV, over a 3-4 hour period. The time, the expense, the invasiveness of the needle and the overall inconvenience has made this therapy out of reach to most people, until now.

Hi, my name is Dr. Rita Ellithorpe; we appreciate your interest in Detoxamin today. As a practicing medical doctor, I understand how demanding our busy schedules can be. My goal is that you find the information on this page direct and to the point, and that you receive accurate EDTA chelation therapy information. We promise to provide you with a clear understanding of exactly what EDTA chelation therapy is, and the preferred modality today, known as Detoxamin. You will also find out why I no longer use IV EDTA chelation therapy in my own clinic and why Detoxamin is given exclusively to my patients.

We are so confident that you will experience better health once you start using Detoxamin;

I understand how important this information is to you as I see patients every day with both chronic and acute health problems. From heart disease, diabetes, high blood pressure, cardiovascular diseases, chronic fatigue, cancer to prostate issues and so many more diseases prominent today, it is apparent that each have one thing in common. They are all linked to our increasing exposure to heavy metals in our environment.

In my clinic, Tustin Longevity Center (TLC), I have found heavy metals in the vast majority of my patients; this is without the patients even knowing that they are carriers of heavy metals in their bodies. This is why for years I have been administering IV EDTA chelation and am fully aware of the problems associated with it. For years I have been looking for a method of EDTA chelation that offered more affordability, more convenience and safety, without losing any effectiveness. I tried Oral EDTA and other methods, and none would compare with the results I experienced with IV EDTA chelation - until I started to use Detoxamin.

Clinically, my patient-population experiences demonstrate improved energy, mood and mental function as these oxidizing metals are reduced with Detoxamin. Detoxamin is the 21st century antioxidant key (along with a healthy lifestyle) needed to survive living in our toxic world.
As a medical authority on Detoxamin, I truly believe Detoxamin is one of the most significant means to improve patients' overall health that I've experienced in my 30 years of practice. And as of now, I have treated more than 600 patients with Detoxamin.

Why are you looking into chelation therapy? We find that the three most common reasons are:
Perhaps you are undergoing IV EDTA Chelation and you are looking for an easier and safer method of EDTA Chelation, without losing the effectiveness of IV therapy?
Perhaps you have heard about EDTA Chelation Therapy from your doctor, friend, relative or neighbor because of your ongoing health problems and that EDTA chelation was recommended?
Or perhaps you have learned about EDTA Chelation Therapy from your own research on the internet and are looking for more information?
Whatever your reason is for visiting us today, we hope we give you what you are looking for.

Detoxamin is an over-the counter, patented EDTA chelation suppository that is medically equal to the IV EDTA method, and has made EDTA chelation therapy accessible to everyone.

The benefits of using Detoxamin are astounding:
More affordable. Detoxamin is 70% less than IV EDTA chelation. Every three Detoxamin is medically equal to approximately one IV EDTA chelation treatment.
More convenient. No more traveling to your doctor's office for the treatment. Simply take one Detoxamin right before bedtime and the EDTA slowly absorbs into your body while you sleep. Waking up to better health is a wonderful thing.

Safer. Detoxamin introduces 750mg of EDTA slowly into the bloodstream and soft tissues, exactly where you need it the most. The dosage does not put the biological burden on the liver and kidneys like IV EDTA chelation does, making it much easier on the body to drain the toxins.
Better EDTA assimilation. Detoxamin introduces less EDTA more frequently, rather than a higher dose less frequently. This provides better EDTA assimilation into the body. This aspect of Detoxamin is what excites doctors the most about the product, as IV chelation puts an unwanted strain on the body.

Medically equivalent to IV EDTA chelation. This is another huge aspect of why Detoxamin is so popular throughout the world. People for years have been frustrated with the inconvenient delivery of EDTA into the body. Now that this method is available, most people prefer it and in most cases the results are even better than with the IV method. For every three Detoxamin, you receive about the same dosage you would get in one IV treatment, but with a much safer and more convenient delivery method.

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Interesting reading Live Blood Cell Analysis is wrong

Live Blood Cell Analysis:
Another Gimmick to Sell You Something

Here on this website you can read today, in english, what claims Pasteur many, really many years ago in french. Im not sure the author of this website is able to understand french.

Have a look here:

It seems for me further, who ever wrote this, doesn't heard anything about germany. I'm agree is far a way from the USA. But doesn't make it sense to see both side of the coins?

I appologize, when the outhor is blind on one his Eys.

Dr. Eddy
Teacher of the Live Blood Cell Coursesat:
http://www.dreddyclinic.com/education/live_blood_3days.htm


Live Blood Cell Analysis:

Another Gimmick to Sell You Something
Stephen Barrett, M.D.
Live blood cell analysis is carried out by placing a drop of blood from the patient's fingertip on a microscope slide under a glass cover slip to keep it from drying out. The slide is then viewed at high magnification with a dark-field microscope that forwards the image to a television monitor. Both practitioner and patient can then see the blood cells, which appear as dark bodies outlined in white. The practitioner may take polaroid photographs of the television picture or may videotape the procedure for himself and/or the patient. The results are then used as a basis for prescribing supplements. The procedure is also called live cell analysis, dark-field video analysis, nutritional blood analysis, and several other names.

Dark-field microscopy is a valid scientific tool in which special lighting is used to examine specimens of cells and tissues. The objects being viewed stand out against a dark background—the opposite of what occurs during regular microscopy. This allows the observer to see things that might not be visible with standard lighting. Connecting a television monitor to a microscope for diagnostic purposes is also a legitimate practice. However, live cell analysis is not. Most of its users are chiropractors, naturopaths, or bogus "nutrition consultants."
Dubious Claims

According to a flyer from a Los Angeles chiropractor:
Live Blood Analysis is a simple procedure for obtaining a quick and accurate assessment of your blood. With only a sample, taken virtually without pain from your finger, [the test] is able to provide a composite of over 25 aspects from your live blood. Darkfield microscopy now allows us to observe multiple vitamin and mineral deficiencies, toxicity, tendencies toward allergic reaction, excess fat circulation, liver weakness and arteriosclerosis.

During 1998, the web site of the Integrated Medical Center, Annandale, Virginia, stated:
Blood is magnified by 30,000 times, giving us the ability to document your condition, monitor your progression while on treatment. The blood is the pathway to the flesh and tells all. Using this technology allows us to monitor your condition and adjust as needed. Your blood is the best place to find quick result and determine if you therapy is effective. Quick response spells maximum results.

"Nutripath" Stephen Heuer, of Sunnyvale, California, claims that great benefits can result from monitoring a special protein:
Live Blood Analysis in a Dark Field primarily monitors the life cycle of a protein called the "Symprotit" or "Prion".

The Symprotit creates health under the right pH conditions or disease under the wrong pH conditions. Within us are the seeds for life or death depending on the environment we create for the Symprotit. Diet, radiation, emotions, and toxins are the four factors which influence this internal environment for life or for death. Much like the butterfly starts out as an egg, becomes a caterpillar, and finally becomes a butterfly, so too can this microscopic blood pritein called the Symprotit/Prion evolve into a bacteria in the blood and then a fungus in the tissues.

Monitoring the life cycle of this protein can give you the correct understanding of biology to help you heal Cancer, Arthritis, Candida, Chronic Fatigue Syndrome, Prostate issues, Multiple sclerosis, Bacterial, Viral and Yeast Infections, Depression, Sleep Disorders, Headaches, Constipation, Excess Body Fat, Potency or Fertility Problems, Memory Problems, PMS, Menopause, and more. Health is attainable when the environment for it is created.

The Innerlight Biologic Microorganism Research Foundation claims that live blood cell analysis can reveal "the level of activity or inactivity of the immune system," various types of "organ stress," and many types of "metabolic dysfunction."

These claims are sheer bunkum. Although a few characteristics of blood (such as the relative size of the red cells) are observable, live cell analysts invariably misinterpret other things, such as the extent of red blood cell clumping, changes in the shape of the cells, and other artifacts that occur as the blood sample dries. Moreover, most practitioners who perform the test are not qualified to manage the problems they purport to diagnose.

During the mid-1980s, one company marketing live-cell equipment projected that a practitioner who persuades one patient per day to embrace a supplement program based on the test would net over $60,000 per year for testing and supplement sales. Another company estimated that with five new patients a day (22 days a month) paying $30 for the test and $50 for supplements, practitioners would gross over $100,000 per year just on initial visits.

The most active individual promoters of live-cell analysis have been James R. Privitera, M.D., of Covina, California, and Joel Robbins, D.C., of Tulsa, Oklahoma.

Privitera claims that "clot malfunction" is an underlying cause of many diseases, can be diagnosed with live cell analysis, and can be treated with large doses of dietary supplements. His book, Silent Clots, describes his "general daily guidelines [for supplements] that have worked well for many patients as an anti-clotting program." The book also describes regimens for arthritis, asthma, baldness, bladder infections, cancer, colds, colitis, cramps, diabetes, diarrhea, diverticulosis, eczema, and edema, and includes case histories of patients he treated for many other conditions [1]. I do not believe there is any scientific evidence for these claims or that these regimens are effective as Privitera claims. His's web site offers more than 150 supplement products for sale.

In 1975, Privitera was convicted of conspiring to prescribe and distribute laetrile and was sentenced to six months in prison. (Laetrile is a quack cancer remedy.) In 1980, after the appeals process ended, he served 55 days in jail but was released after being pardoned by California Governor Jerry Brown. (The pardon occurred in response to a letter-writing campaign generated by the National Health Federation, a group that espouses what it calls "health freedom.") Then, because Privitera had been prescribing unapproved substances (including laetrile, calcium pangamate, and DMSO) for the treatment of cancer, the California Board of Medical Quality Assurance suspended his medical license for four months and placed him on ten years' probation under board supervision.

During the probationary period, Privitera was "prohibited from making any representation that he is able to cure cancer through nutrition." He was also forbidden to tell patients they had cancer unless the diagnosis was confirmed in writing by an appropriate board-certified specialist. During the probationary period, Privitera commercialized live-cell analysis and founded two companies that marketed devices for doing it. Silent Clots mentions that in 1993, a federal judge signed an order authorizing Internal Revenue Service agents to enter his clinic premises to effect a levy and that a seizure was made. However, the book provides no further details about his tax-related difficulty.

In 1999, Privitera was implicated in the death of a 71-year-old woman who had consulted him for arm pain. While in Privitera's waiting room, she complained of a headache while in Privitera's waiting room. Documents in the case state that Prviitera (a) prescribed 20,000 units of heparin (an anticoagulant) to be placed under the woman's tongue, (b) examined a blood sample with a dark-field microscope, (c) concluded that the blood specimen showed too much tendency to clot, and (d) prescribed another 20,000 units of heparin to be given under the patient's skin. Soon afterward, the patient became lightheaded, vomited, and passed out. She was rushed to a hospital. where it was noted that she was comatose and was bleeding from several places. She died a few hours later, apparently as a result of a massive hemorrhage inside her head. In 2003, the Medical Board of California charged that Privitera had (a) failed to properly evaluate the woman's headache, (b) had no documented rationale for administering heparin, and (c) had administered an overdose [2]. The case was settled with a stipulation under which Privitera agreed to be reprimanded, pay $5,000 for costs, and take courses in prescribing and medical recordkeeping [3].

Robbins graduated in 1978 from Cleveland Chiropractic College in Kansas City, Missouri, but he also claims to have a Doctor of Naturopathy (ND) degree from the Anglo-American Institute of Drugless Therapy and a Doctor of Medicine (MD) degree from the British West Indies College of Medicine. The Anglo-American Institute of Naturopathy was a British diploma mill that issued credentials to people who completed mail-order lessons, submitted a thesis, and paid a modest fee. The "British West Indies College of Medicine" was not an actual school but was a scheme created by con man Gregory E. Caplinger to defraud chiropractors of "tuition" money [4]. In 1996, Caplinger was arrested in Florida on ten counts of racketeering and grand theft, but the charges were withdrawn after he made partial refunds.
Dubious Conduct
During the mid-1980s, National Council Against Health Fraud vice president James Lowell, Ph.D., watched three practitioners demonstrate live cell analysis at health expositions. Lowell noted:
None took precautions during the preparation of the slides to prevent the blood from drying out or clotting.

They failed to clean their microscope slides carefully between patients, which meant that dirt seen under the microscope would be misinterpreted as blood components.
Some of the patterns one practitioner saw resulted from his microscope being out of focus and disappeared when Lowell adjusted it properly. [5]

Live cell analysis has also been promoted by Infinity2, of Scottsdale, Arizona, a multilevel company whose distributors often demonstrate their wares at chiropractic conventions. Infinity2 called the test "live cell microscopy" or "Nutritional Blood Analysis" and recruited licensed health professionals to use the procedure to sell its products. In 1995, I was tested at a national chiropractic convention where two teams of Infinity2 distributors had exhibits. One exhibitor said I had "mild B12 deficiency" and "maldigestion" that could weaken my immune system and cause fatigue. The other said my blood cells showed evidence of "liver toxicity," "bacterial infection," and "free radical damage."

In both cases the recommended "treatment" was enzyme pills, which the company was marketing with false claims that "enzyme deficiency" is widespread among Americans. To reinforce their that the pills could help me, both practitioners gave me enzyme pills, repeated the procedure several minutes later, and said that the problems were no longer visible. Unknown to them, however, I had faked taking the pills, so the "improvements" they saw had nothing to do with them. The most likely explanation is that the specimens were examined differently. Blood dries more quickly near the edges of the slide than near the center. Thus "improvement" will occur if the first specimen is examined near an edge and the second specimen is examined near its center. Company literature listed Joel Robbins as a member of its Professional Advisory Council.

I asked both exhibitors whether the test procedure is covered under insurance policies. One—a naturopath—said he routinely billed the test as a regular office visit and also used eight CPT codes, including B12 testing for deficiency. he also said that Infinity2 ran training sessions on how to do the testing and billing. The other exhibitor did not confirm that the course included "creative billing" ideas, but he said that he knew that some doctors were billing the test as regular visits. Some live-cell practitioners are using the procedure code number for "dark-field microscopy" when they submit insurance claims forms. Doing any of these things would be insurance fraud.

Regulatory Actions
In 1996, the Pennsylvania Department of Laboratories informed three Pennsylvania chiropractors that Infinity2's "Nutritional Blood Analysis" could not be used for diagnostic purposes unless they maintain a laboratory that has both state and federal certification for complex testing [6]. The company's attorney replied:
As background, you should know that part of our business activity is supplying a microscope system that is equipped for the demonstration of blood samples on a video monitor. We teach and recommend the use of this system as a health education demonstration. In our training and system we do not teach, promote or address in any manner using the system for "analysis" or any other medical purpose.

Our system is based on obtaining a written nutritional and lifestyle analysis from patients of doctors using the microscopy system. Once this questionnaire and evaluation of lifestyle and nutrition is examined by the doctor, the doctor then makes specific recommendations to the patient, based solely and exclusively on the nutritional analysis and personal interview with the patient.

After any recommendation has been made for altering the patient's lifestyle or nutritional habits, the doctor may place a single drop of blood on a sample slide for viewing through the dark field microscope which is then displayed on a video monitor.

This demonstration is a powerful motivating tool to encourage a doctor's patient to accept the doctor's previously made recommendations and alter his or her lifestyle to a healthier form of living.

The doctor performing the demonstration never makes any analysis, determination or recommendation based on the video demonstration. There is no commentary given regarding the state of the patient's blood or anything seen in the bloodstream itself other than to educate the patient by pointing out features of the blood such as red cells, white cells, and plasma. The patient is able to view a sample of his/her own blood, which results in the motivation that can lead to beneficial lifestyle changes for the individual patient [7].

A Laboratory Department official then informed the attorney that certification would be required if the practitioner:

Either prescribed a nutritional supplement or changed the amount or type of a supplement based on viewing a blood sample.

Recommended lifestyle or nutritional changes based on viewing a blood sample.
Performed nutritional microscopy more than once for a given patients.

Compared the patient's blood smear to that of another slide or picture
Showed the patient's blood smear and making any comment or providing any information other than to point out features of the blood such as red cells, white cells, and platelets [8].

Federal certification of medical laboratories is governed by the Clinical Laboratory Improvement Amendments (CLIA) which Congress enacted in 1998 to establish quality standards for all laboratory testing to ensure the accuracy, reliability, and timeliness of patient test results regardless of where the test was performed. In 1996 and 1997, the Health Care Financing Administration (now the Centers for Medicare & Medicaid Services) Office of General Counsel determined that live blood analysis was a "high-complexity" text and was subject to stringent CLIA requirements. Failure to comply with any of these requirements will result in enforcement actions and/or sanctions being taken.

In 2001, the HHS Office of the Inspector General issued a report on regulation of "unestablished laboratory tests" that focused on live blood cell analysis [9]. In 2004, the Centers for Medicare & Medicaid Services issued a special alert which stated that any facility performing live blood cell analysis must have CLIA certification for high-complexity testing [8]. Very few practitioners who do live blood cell analysis would have reason to seek laboratory certification; and if they did, I doubt that they would get permission. However, the states have jurisdiction over whether noncompliant laboratories are permitted to remain in business.

In 2005, the Rhode island department of Health ordered Joyce M. Martin, D.C., to stop performing live blood analysis. An attorney for the state Board of Examiners in Chiropractic Medicine described the test as as "useless" and a "money-making scheme " A state medical board official said that the test has no discernible value and the public should be very suspicious of any practitioner who offers it [11]. Edzard Ernst, M.D., Ph.D., a professor of Complementary Medicine at the University of Exeter, summed up the situation in an article in the British Guardian:

Seeing one's own blood cells on a video screen is, admittedly, a powerful experience. It gives patients the impression of hi-tech, cutting edge science combined with holistic care. And impressed patients are ready to part with a lot of money. American websites explain how a practitioner can make $100,000 (£57,000) annually by purchasing the equipment necessary for performing LBA. The bulk of this money is made not through charging for the test itself but by selling expensive nutritional supplements to the patient with the promise that these will correct whatever abnormality has been diagnosed.

In other words, patients are potentially cheated three times over. First, you are diagnosed with a "condition" you don't have; then a lengthy and expensive treatment ensues; and finally the bogus test is repeated and you are declared "improved" or "back to normal." [12]
If you encounter anyone who performs any type of live cell analysis, please report this to your state department of laboratories and send a copy of your notice to me at P.O. Box 1747, Allentown, PA 18105.

References
Privitera J, Stang A. Silent Clots: Life's Biggest Killers. Lockstep Medicine's Conspiracy to Suppress the Test That Should Be Done in Emergency Rooms Throughout The World. Covina, Calif.: The Catacombs Press, 1996.
Accusation. In the matter of the accusation against James R. Privitera, Jr., M.D. Before the Division of Medical Quality, Medical Board of California, Department of Consumer Affairs, State of California, Case No. 11-2001-119360, March 31, 2003.
Stipulated settlement and disciplinary order. In the matter of the accusation against James R. Privitera, Jr., M.D. Before the Division of Medical Quality, Medical Board of California, Department of Consumer Affairs, State of California, Case No. 11-2001-119360, signed May 7, 2004, adopted by Board Oct 7, 2004.
Kelly S. DCs lured to foreign medical school.
Dubious goings-on down Santo Domingo Way. Dynamic Chiropractic Archives, Jan 1, 1993.
Lowell JA. Live cell analysis: High-tech hokum. Nutrition Forum 3:81-85, 1986.
Wlazelek A. Chiropractors cease blood cell show and tell. State restricts the use of magnified images to sell vitamins, supplements. The Morning Call, April 12, 1996, page B6.
Woodruff SM. Letter to Joseph W. Gasiewski, Director, Division of Laboratory Improvement, Pennsylvania Department of Health, Jan 17, 1996.
Gasiewski JW. Letter to Samuel M. Woodruff, General Counsel, Infinity2, Feb 16, 1996.
CLIA regulation of unestablished laboratory tests. HHS Office of the Inspector General, July 2001.
Barrett S. CLIA hits questionable tests, Quackwatch, March 9, 2004.
Freyer FJ. Chiropractor ordered to halt blood tests. Providence Journal, June 21, 2005.
Ernst E. A new era of scientific discovery?

Intrigued by the spectacular claims made for Live Blood Analysis? Don't be. It doesn't work. The Guardian, July 12, 2005.
Additional Proponent Sites
Center for Enzyme Therapy (offers "board certification" as a "holistic health microscopist," a credential not recognized by the scientific community.
NuLife Sciences (site contains photographs of blood examined with darkfield microscopy)

Real Biology Alone Can Solve the Riddle of Cancer

by Prof. Dr. Günther Enderlein, Hamburg, Aumühle, Germany, Member of the Society for Freedom in Science at Oxford. ©Copyright 2001 by The Enderlein Group
If the chemist Professor Dr. Otto Warburg (Berlin) believes to have solved the riddle of cancer as a result of damage done to the chronic cell-breathing (In: Die Naturwissenschaften, 1954; Hamburger Abendblatt, dated 24.12.1954) then the "Christmas surprise" may rather be found in his -a Nobel-prize-holder - falling a victim of one of the numerous "watchwords" of doctrinal dogmatic dictatorships. This watchword runs as under:"Hundred different agitators of cancer cannot be valid. As a consequence thereof there is none at all."This catastrophic illogical standpoint, however, is even still surpassed by the still more catastrophic illogy of putting it into a question, which believes to be in a position to put off comparing morphologic questions with physiological answers. And on this convulsing "logic" - quite in the sense of the remonstrances of the comparing morphologist Leuckart against the Leipzig physiologist Ludwig (cf. Zeitschrift für wissenschaftliche Zoolog. 2. 1850) - O. Warburg is building up a fancy edifice of biologylessness.
A logical inference would be:
The conditional causes of the cancer and of all the chronic diseases are the 350 cancerogene substances and factors among them, above all, the albumen-over-feeding-diet, fattening the originator into pathogene phases.The inference (consecutio) of the conditional and causal causes, "the want of oxygen" O. Warburg declares as a "chronic damage to cellbreathing" and in a simultaneous want of every logic and every biological base as a "cause" of the cancer! (Neue Post, Düsseldorf, dated 5.2.1955). Thus: more clearly amplifying explanations about the nature of the cancer-disease itself, that are the documents for the causal causes of the cancer for the Nobel-prize-holder. That are juggler's tricks. It is a token of our time to consider waste-paper-mass-production for journals as the essence of the propaganda of enlightenment, which, however, is only adapted to waste foolishly time, paper, composition, printer's ink and public means of the nation.The causal causes represent the lasting permanency of a microorganism from primitive times, which is peculiar to all mammals, and which the original cultures define as a "degeneration of the juices of the body" (humoralpathology) and this, above all, even then, when diet and conduct of lives of men in an increasing measure offered cause that this original parasite (Endobiont) was in an increasing fattening state.The quite severe exigency of real biological considerations of the cancer problem is the observance of this road of perception, altogether in conformity with the knowledge of Pierre Delore, professor of the faculty of medicine in Lyon. "The science of health in its principal condition is an affair of biology" (vide: "Notre Frère Corps", Paris 1938, page 58). The absolute knowledge, next of all and above all, is tied to the conditional causes, a way, which the original cultures have taken since perhaps twenty-thousand years and which they felt entitled to consider as "causal". Hippocrates was the last who still defended this. Only Hahnemann one and a half centuries ago still thought to stir this up to fresh life again, however the real "causal cause" was missing viz., the agitator microbe, which they did away with after the pattern: "they couldn't see the wood for trees" by a very simple manipulation, viz. By one of the "thousand watchwords". Should this even come from the "Pandora's box"?In order to ascertain the value of the guidance of the chemist O. Warburg, who believes to solve and to exhaust the "riddle of the cancer by preventing breathing of the cells", one has to go a little farther back, for with only disciplines of another kind without any biology there can never be obtained a biological scope.The nature of the "chronic damages of the cell-breathing" naturally refers to disturbances of the change from two-valued iron into a higher valued one. The first who had pointed out to the fundamentally important fact of the disturbance of the circulation of iron in case of cancer was Spude in his theory of avidity, which he had already laid down in 1904 and which two years later was taken over by Fischer-Wasels. H. Dechow (Arch. For history of development of bacteria, Vol. 1, Part. 2, 1933, page 147) in 1933 had called special attention to the difference between a cell of the cancer and a normal cell would be as follows:"The cell of body breathes - the cell of cancer ferments."
This had been formulated by me in the following further development:
"For the organism of the host, cancer is a fermenting and decaying state, obtruded by a parasite - a fungus - and its shapes of development" whereby also Dechow's opinion is declined that the so-called cell of cancer should be the parasite itself. Warburg already decenniums ago had proved that in each cancer-tumor lactic acid is formed up to ten times the quantity of the normal content of lactic acid of the human tissue. Which physiological importance this increased content of lactic acid possesses, has been closely developed by me in 1950 (Immunobiologica, Vol. 3/4, pages 94-101) viz. On the basis of the"anartatic fundamental law", of the law of dependence of the ascending (probaenogenetic) tendency of the primitive phases of the microbe to confederations for higher and highest phases of the descending pH-value of the microorganism itself and of his surrounding nourishing medium. That means nothing else than that this microorganism creates for himself the ground in order to render feasible its higher phases of development. These formations of acid for this purpose are by all means of species specific nature that is to say therefore, that each kind forms its own organic acids in order to render possible the ascending tendency (probaenogeny) at all. It is well known that the lemon acid in the market has never seen a lemon. It rather descends from the culture of Aspergillus niger van Tieghem, which are technically cultured by special institutions. As an example this is also the case with Penicillium notatum, the "Penicillin-acid". As we see it is here the question of acids of the organic chemistry. Thus we are approaching the deciding question which runs: what for a part acts the presence of up to ten times the quantity of lactic acid not only in the tumor, but also in the whole blood as well as the liquids of the body (part of deterioration of blood of the tumoral-pathology!) of a she-cancer-patient? Well, the answer represents itself as a very simple one: it is the factor of the microorganism Mucor racemosus Fresen, (of the Endobiont in direction of the descending pH, in order to arrive at a higher state of development on basis of the anartatic fundamental law. Upon page 99 l.c. a sketch has been brought by me, which symbolizes these proceedings in scheme. By this constant formation of organic acid in question in this manner the primitive phases will be gradually brought over to the phases of bacteria and finally the phases of bacteria into the phases of fungus. For this rise, however, interior valences (values) gradually must be built up, which deliver the substance for the higher confederations of the primitive phases; this process is one of the factors of increasing the gravity of sickness and - formally inverted are, proceeded in the opposite way, viz. Descending from the higher phases of development to inferior and to the primitive phases valences (values) are available in order to diminish themselves to more primitive phases. Hence such a trial is very simple, which was again and again pointed out by me as the most simple proof of the uniformity in the specific sense of:"phases of fungus" - "phases of bacteria" - "primitive phases".For, adding 5% of a solution of soda or double carbonate of soda the Chrondit-state will at once spring forth both from the bacteria and fungus-mycel, viz. In the shape of long scortches (fila) with tiny button-endings of a Symprotite (primitive granule). I have already pointed out in 1933 in "Ende der Herrschaft der Zelle als letzte biologische Einheit" (Arch. Entw. Bakterien I, 2, pages 171 to 179, Illustration 5.) [published in Explore!, Volume 6, Number 1, pgs. 4 - 7 as "The End of the Cell's Dominant Role as the Ultimate Biological Unit"] as well as in 1943 in "Cancerologica I" Arch. f. Entwicklungsgeschichte der Bakterien). In Immunobiologica, vol. 3/4 (1950, page 115), it has been displayed by me, how the further correlations of these downright biological questions could only be accounted for by the discovery of the "yellow ferments", which follow the oxygen communicating iron. (O. Warburg and W. Christian, Biochem. Zeitschr. 254, 438, 1932). The investigations of Botelli and Stern proved that the accessorial breathing, which f.e. takes place in totally cleared juices of yeast, represents a transfer of oxygen by yellow ferments, which during the extraction of the cells separated by the insoluble iron system, laid open and become oxygen transferring ferments. The knowledge developed by Warburg (1924) that the molecular oxygen, which disappears in the breathing of the aerobe cell, never reacts directly with the biologic phlogiston, but only and exclusively with complex bound two-valued iron. This opinion revised fundamentally the opinion of Justus von Liebig (Tierchemie 1843) that the iron of the hemoglobin should oxidize the biological fuels in the blood, hence a confusion of transport of oxygen and combustion, between hemoglobin and catalytically powerful cell-iron. And the higher valued iron thus created will be re-reduced by the organic substance to two-valued iron. The oxygen in the cell-breathing is transported by the change of valence of a complex iron combination, by it the iron is the oxygen transporting constituent of the breathing ferment. Later on it has been found the catalytic activity of the haemine, which rests upon the constituents of iron, in numerous organisms also of vegetable nature, which appear in red, green and mixed-colored, and also represent the essential constituent of the chlorophyll.Still there remains the critical step to embrace all this knowledge. So we find that the primitive parasite - the Endobiont - in all its manifold shapes of appearance always represents the cause, by its constant activity in forming lactic acid in cases of cancer, with the entire complex of Endobiosis of chronic diseases, to undermine and remove the catalysator-activity of the iron by chemically binding of the iron. And then so there arises: lactic acid iron oxydul: "Fe (C3H5O3): 3 H2O". Whilst the lactic acid is playing a fundamentally important part of digestion in the stomach and in the intestinal tract, the pathological state of the formation within the cancer-tumors and within the tissue of the patients sick of Endobiosis is of catastrophic issue as to anaemy and deficient nutrition of oxygen, and as a climax entire suffocation with lethal issue.Since just in the case of cancer any combustion has been reduced for want of oxygen, a strongly reduced formation of lactic acid should be reckoned with a cancer-sick organism. This, however, is not at all the case as is documented by the up to tenfold formation of lactic acid in case of cancer. This secretion of lactic acid rather is a private enterprise of specific nature of the Endobiont: Mucor racemosus Fresen. It also represents the causal cause for this, namely quite in the frame of the anartatic fundamental law, according to which each and every microbe is compelled to form its specific acid in order to ensure its cyclic ascendence (probaenogeny).An artificial addition of haemines, beyond a doubt, will result in a reduction of the deficiency of oxygen owing to the want of iron as a catalysator. Wolrad Schotten recommends the intravenous injection of iron oxyduloxyd in the shape of fine grain to fight these two deficiencies, which practical application I have had a chance in getting acquainted with in earlier times with a physician in Berlin-Zehlendorf. The iron grains, by no means very fine, for a long time work in the cell-plasma in this condition as catalysators for the oxygen-housekeeping. Presumably during this time of staying in the shape of grains, traces of the iron are transformed into haemines, which then in the "status nascendi" are in a position to develop a livelier activity (cf. Immunobiologica, Vol. 3/4, 1950, page 116). By that, anyhow, no healing of the cancer has been achieved, not at all. The Waerland-diet, however, by a strongly increased supply of fresh salads of all kinds not only furnishes the possibility to do away with the deficiency of iron and simultaneously of oxygen by the increased supply of chlorophyll, but - on the other hand - quite in general, by keeping away animal albumen and, above all by strictest vegetable diet, to meet the insatiable hunger of albumen of the Endobiont, consequently preventing its fattening into higher stages and valences, and to deliver it up to quite a natural reduction. It may still be noted that two-valued iron contains aerosan, which is also applied by some physicians in case of cancer.Chemo-therapeutic measures oppose the bipolarity of the causal microbe by an immense resistive capacity, so that the human cells then would obtain a far greater damage. The "organic acids" of all antibiotica including Sanamycin (cf. D.M.W. 80, Year No. 1, 20.1.1955, pages 140-143) as well only can change the symptoms temporarily, whilst the sickness will be impaired by seeming healing (cf. J. Zinsius: Die Antibiotica and ihre Schattenseiten, 1954). So there is nothing left but a pure biological measure, viz. Making amends for the primitive phases and live-colloids, gone lost by the diet of civilization and the conduct of life, which alone are adapted for removing the higher phases of development in connection with an increasing pathogenity, indeed the former copulation with the primitive kernels (Mych) of the higher phases.This is the way to remove the primitive parasite Mucor racemosus Fresen with all its many hundreds of shapes of development and valence of development by real biological proceedings.As to the trials of Harry Goldblatt and Gladys Cameron in the United States, to change normal cells of body of tissue cultures of 2-1/2 years and a periodical withdrawal of oxygen in tumor cells, this rests upon the fact that every cell of the body of all mammals harbors the Endobiont in any primitive stage and that these, when thus barbarically treated, are no more in a position to raise the requisite means of defense in order to stop sufficiently the probaenogeny and the increase of the Endobiont. Years ago already I have repeatedly pointed out to a ridiculously simple trial to arrive at the same end with cells of the body. If one takes the blood from the venules - whereby it is all the same, whether the blood is taken from cancer-sick patients or from quite healthy persons - only 12 - 14 days after having taken the blood from the patient, storing the venule during this time at room temperature, if you then watch the Erythrocytes under cover glass, one will find that the red blood globules have been completely hollowed out by the swarming Chrondites of the Endobiont, that therefore the albumen of these blood cells have been entirely consumed by the Endobiont, the causal cause of the cancer, and these phases already watched and exhaustively dealt with by sanitary counselor Dr. Med. Otto Schmidt in Munich 1903, describing them as "Schwärmerchen" i.e. little swarmers, carrying out very vivacious dances of copulation within the Erythrocytes.Well, since more than half a century the epigones of this man then have completely ignored the shapes of this Chrondit-stage, exactly described by Schmidt and even the expert for blood research, Professor Dr. Med. Hans Franke (Berlin) in his "phase-contrast hematology" did contrive to comprehend the lively mobility of the phase of the typical Chrondit-picture consisting of long Filum with numerous divers Symprotites primitive kernels distributed over the length of the Filum as Brown-molecular-movement (f.i. in fig. 13 and 14, though these throughout typical shapes have already been presented in the shape of photos by the Archives for the history of development of bacteria, vol. I, part 3, 1937, page 193 in figure 3 in a lively movable state and in figure 1 and 2 in a stiff motionless state. Every biologist would have isolated the shapes at once and would have bred them upon nutrient agar and in liquid fostering.How many termini of cell shapes of anomalous nature already refer to the "workshop of the Endobiont alone for the preparation of the tumor-formations" viz. Upon the marrow of the bones! They prove step by step the loss of capacity of cell-division by the constant attack of the parasite, the Endobiont, and its enhancing of the valence and of the phases of development, so f.i. of the chain kernel cells, which reach fingerlike far into other tissues and can also be met in tumors which, however, biologically speaking correspond with the Myelocytes of the marrow of the bone and of the blood, and represent the expression of the reaction of the irritation upon the strong multiplication of the parasite, which the cells believes to evade by hastiest divisions. The potency of it is exactly the Megacaryocyte of Metschnikow, likewise in the marrow of the bone, which harbors immeasurable quantities of parasites, and which consequently take over the function of transformation of the Symprotites into thrombocytes in the like manner, as the befallen Erythrocytes of the blood, and on the other hand in the extreme the direct formation of Mycel of the Mucor racemosus Fresen as reported already by Tissot (1925) and illustrated in fig. 27 by Enderlein (Arch. Entw. Bakt. 1.5.1937, page 209). As we see the flowing happening of this primitive parasite is boundless. A further product of the unusual befall of Endobionts of the marrow of the bone are the Normoblasts and the Megaloblasts, with which the befall of Endobionts ascends to a colony-like gathering the pseudo-kernel. Transitions of it are the Reticulocytes, which show forth a wide dissemination in the blood.The boundless heaping of high-valenced parasites thus revealed represents the causal cause that Bogomoljets had exactly chosen this material to start with for his serum, though neither he nor Niehans never have had the slightest idea of the true nature and virtue of their preparations, which prove to be of a quite isopathic nature. All these boundless possibilities of the different valences and phases of development of the parasite in the total amount of cells of the human body represent at the same time also the biggest share of the so-called "constitution", whereby a substantial part of this terminus has further developed itself into a considerably more palpable factor.Again and again I have pointed out the practiced methods exercised by some disciplines, standing as outsiders of the biology and systematically paying no heed to the fundamental biological facts. Some of the most important moments may be repeated hereafter. Here are to be found the biological "proves", again and again demanded by the gentlemen of the doctrine since decenniums, which are fully answered since almost half a century.The fact that Fontes (Mem. Institut. Oswaldo Cruz, I, 2, 1910, page 186) proved as the first the infectuosity of the filtrate of tuberculous material, C. Nicolle (Bulletin de l'institut Pasteur XXIX, 1931, pages 209-224, 273-280) interpreted these already as separated phases of development, H. Dostal (Wien. Mediz. Wochenschrift, Vol. 60, 1910, pages 2098-2100 and Vol. 63, 1913) in addition still confirmed the ball-shaped Basit-stage, and Enderlein (Arch. Entw. Gesch. Der Bakterien, Vol. I, part 2, 1931, pages 6-13, 53-105, Table 1 and Illustration 76) already a voluminous circulation covering three groups of phases: "primitive phases - phases of bacteria - phases of fungus", as well as in: "The End of the Cell's Dominant Role as the Ultimate Biological Unit" l.c. Vol. I, 2, pages 171-179, July 1933) that that "Omne vivum ex ovo" *(Harvey 1651) as well that "Omnis cellula e cellula" excludes for good, are ample documents.It is insignificant to enter closer into the main treatise and the numerous reports (f.i. Hamburger Abenblatt, dated 8./9.1.1955, Hamburger Morgenpost, dated 10.1.1955). Worthy of notice is only the very dexterous concession for a retreat of Otto Warburg in the last mentioned paper. "There is no producer of cancer, that enters the body from without", which can be fully confirmed, for all chronic diseases inclusive of cancer are by no means diseases of infection, but the exciter of microbes in the most primitive times during the shaping of these mammals, had been infected to all these mammal-primitive-shapes, and since that time lives with all mammals as a permanent parasite in order to produce with its thousands of phases of development (probaenogeny) always stronger pathogenities and also on this route, to let arise thousands of forms of maladies. It is therefore the question of gradual building up of the always present permanent-parasite to higher and always stronger pathogene shapes from positively apathogene primitive phases (scanty valent Symprotites + colloids) to a befall from within.Totally corresponding with the knowledge of the primitive cultures up to Hippocrates, viz. A synthetic mode of contemplation of nearly twenty thousands of years, which then was succeeded in turn by an analytic mode of contemplation of two thousand five hundred years. And the success is formulated hereafter:"Disciplines, which educate blindness against biological laws of nature by 'watchwords', will never be capable of solving the problem of cancer and of all chronic diseases."