Abstract
While studying patients with Electromagnetic Field Hypersensitivity, Pre-Alzheimer’s Disease, Alzheimer’s Disease, as well as Autism and abnormal mental & motor dysfunction in children, the author found that the following findings are common among these patients:
A marked increase in metal deposits such as Al, Hg and Pb in the brain, particularly, the Hippocampus area or motor cortex (if abnormal motor function exists), or Pons (if the abnormality is depression and irritability with markedly decreased Serotonin). A marked decrease in Acetylcholine often reaching less than one 5th of normal concentration and often reduced to less than 350 μg compared with the normal range of 1500 μg - 5000μg); when Acetylcholine in Hippocampus decreases to below 350μg, most of the patients develop various short-term memory deficits. If a similar decrease happens at the motor cortex, often abnormal motor functions including Dystonia and sometimes convulsions occurs. Viral infection with or without bacterial infection. A strong negative (-) Qi from both hands.
When excessive metal deposit of Al, Hg, & Pb exist in the brain, they may function as multiple micro-antenna and absorb the environmental Electro-Magnetic Field and create a microinflammation and reduce Acetylcholine in the surrounding nervous system. In the presence of infection, Acetylcholine further diminishes with localized circulatory disturbances with increased Thromboxane B2.
The most common infections found in these patients were Cytomegalovirus, Human Herpes Virus Type 6, Chlamydia Trachomatis and Mycobacterium Tuberculosis. In addition, if the patient also has a headache in one side of the head, then the most common cause is Herpes Simplex Virus Type 1, and occasionally Mycobacterium Tuberculosis can also create a headache in one side of the head. If a headache exists in both sides of the head, then usually one side of the head has a Herpes Simplex Virus Type 1 infection and the other side of the head has a Herpes Simplex Virus Type 2 infection. Less frequently, both sides of the head will have a Mycobacterium Tuberculosis infection which causes a headache in both sides of the head.
For all of these viruses, mixture of EPA and DHA in a gelatin capsule made from Omega-3 fish oil is natural and very effective. For Chlamydia Trachomatis, Erythromycine, Azithromycin, Doxycycline & Substance Z are very effective, but only Doxycycline & Substance Z are compatible with mixture of EPA & DHA.
When these viral infections are treated 4 times a day with a mixture of EPA & DHA as effective, safe, anti-viral agents, and excessive deposits of metals are removed from the brain by giving Cilantro using “Selective Drug Uptake Enhancement Method” (developed by Omura, Y in early 1990s to selectively deliver the effective medications to the pathological area, by stimulating accurate brain organ representation area with acupuncture or other means at the 1st distal segment of the middle fingers, corresponding to the pathologic area of the brain), Acetylcholine often markedly increased in the brain with decreased (-) Qi, and significant improvements in memory and other brain functions and behavior occurred within 1-2 days. If additional bacterial infection such as Chlamydia Trachomatis co-exist, to get further improvement, Doxycycline or more effective Substance Z (Hayashibara Biochemical Lab., Okayama, Japan) was given together with mixture of EPA & DHA using “Selective Drug Uptake Enhancement Method” with various stimulation including application of (+) Qi-Gong energy stored paper without Cilantro because Doxycycline and Cilantro cancel each other’s effects. But if additional Mycobacterium Tuberculosis infections co-exists, both Isoniazid and Rifempin, which are effective for Mycobacterium Tuberculosis, cancel the effects of EPA & DHA, as well as the effect of Doxycycline and Cilantro, and therefore these medications cannot be given together. However, in the early 1990s, the author found that Saiko-Keishito (Tsumura Japanese Pharmaceutical Company, product No. 10) is compatible with EPA & DHA as well as Doxycycline. Therefore, this combination of EPA & DHA and Saiko-Keishito is also successfully used for simultaneous treatment of cancer with coexisting Mycobacterium Tuberculosis with alternative use of a combination of EPA & DHA, Cilantro and Selective Drug Uptake Enhancement Method by applying (+) Qi-Gong energy stored paper.
In pre-Alzheimer and Alzheimer’s disease it is well known that among characteristic abnormal findings in the brain, the following factors are included: 1) Marked decrease in Acetylcholine, 2) Excessive deposit of Al, 3) Excessive deposit of β-Amyloid (1-42). Using the Bi-Digital O-Ring Test Resonance Phenomena between 2 identical substances it has been possible to non-invasively study abnormal changes in Neurotransmitters such as Acetylcholine, Serotonin, Dopamine as well as β-Amyloids, Al, Hg, and Pb since 1990. According to our clinical study in the majority of normal individuals Acetylcholine in most parts of the brain including the Hippocampus area is at least 1,500 μg but most individuals develop recognizable symptoms when Acetylcholine is reduced to less than 300 μg. But in pre-Alzheimer’s & Alzheimer’s patients amount of Acetylcholine often goes down below 200-100 μg. In these patients, wherever Acetylcholine reduces in the brain, corresponding deficiencies show up as recognizable symptoms, characterized by the dysfunction of the anatomically specific location in the brain. Metals, particularly Al and Hg, are often increased significantly anywhere between 350mg to 550mg with or without significant increase in Pb deposit. When excessive metal deposits exists, Acetylcholine almost always reduces. When β-Amyloid(1-42) increases beyond 4 or 5 ng with decreased Acetylcholine, often the patient shows various degrees of short term memory deficiency. When β-Amyloid (1-42) increases over 7 ng, the patient often shows a recognizable deficit of short teim memory. Based on these findings the author established criteria to screen pre-Alzheimer’s disease and Alzheimer’s disease quickly and non-invasively by measuring the amount of Acetylcholine, β-Amyioid(1-42), Al, Hg & Pb. Those who have a significantly reduced Acetylcholine can often be reversed by giving 100 mg of Cilantro tablet wife the “Selective Drug Uptake Enhancement Method” to selectively deliver medication to fee brain by stimulating organ representation area of the entire brain on first segment of fee middle finger of both hands. When the first segment of the middle finger of both bands (which represents the entire brain and face) is stimulated continuously and effectively more than 20-30 minutes, the amount of the Al, Hg, or Pb reduces to about 10% or even lower % of the original excessive amount, which was anywhere between 350mg to 550mg. However, Selective Drug Uptake Enhancement Method becomes effective only when the ipsolateral side of the accurate organ representation area corresponding to the pathological area is stimulated effectively, and the drug can be selectively delivered to the pathological area to be treated. Similar result can be obtained by the stimulation of organ representation areas of tongue by Red spectral irradiation from L.E.D. When this happens Acetylcholine often increases anywhere from about 20% to 100%, but β-Amyloid (1-42) usually did not decrease significantly by removing excessive metal deposit. Even when Acetylcholine increases over 500μg and goes up close to 1500μg, if β-Amyloid (1-42) remains high usually very little improvement of short term memory can be observed. In these patients often multiple bacterial and viral subclinical infection co-exist. Among the most commonly seen causes of the infection include Cytomegalovirus virus, Human Herpes Virus Type 6, Chlamydia Trachomatis, Mycobacterium Tuberculosis, Pseudomonas Aeruginosa and α- Streptococcus. While we are treating these infections in the brain after removal of excessive metal deposit, which is essential before treating infections, as an excessive deposit of metal often inhibits anti-bacterial and anti-viral agents. While studying the effect of the treatment of these multiple subclinical mixed infections of the brain in 2001, the author discovered that when strong Chlamydia Trachomatis infection in the brain is significantly reduced, β-Amyloid (1-42) also markedly reduced, which resulted in significant improvement in short term memory deficiency provided that Acetylcholine has also been sufficiently increased after removing excessive metal. It is also interesting to note that those people with increased β-Amyloid (1-42) in the brain often develop so-called brownidi age spots around the side of the face. The author found in this darkened pigmented area, both β-Amyloid (1-42) and Chlamydia Trachomatis are markedly increased as in the brain. In conclusion, our study indicates that the major cause of increased insoluble β-Amyloid (1-42) protein in pre-Alzheimer’s patient and Alzheimer’s patients is due to extensive Chlamydia Trachomatis infection of the brain, particularly in Hippocampus area. Therefore once these disease is detected by this method, increased β-Amyloid (1-42) protein can be reduced significantly by treating Chlamydia Trachomatis with Doxycycline or Substance Z along with EPA & DHA as an effective anti-viral agent, as most of the patients have simultaneous viral infections. In order for the treatment to be effective, one first have to remove the excessive metal deposit using the Selective Drug Uptake Enhancement Method with Cilantro, and EPA & DHA and Trimox, if there is additional viral and bacterial infection; this treatment often increases Acetylcholine and then follow with the treatment of Chlamydia Trachomatis by Doxycycline or Substance Z and other compatible medications, since Doxycycline is the commonly available effective antibiotics against Chlamydia Trachomatis, but it is also compatible with EPA & DHA and Trimox. Since 2001, with our method, we have been very successful in reducing or almost completely eliminating excessive Al, Hg & Pb and reduce water insoluble β-Amyloid (1-42) to normal value and increase Acetylcholine. However, when treatment is given within 1 or 2 years from the first diagnosis, we were often able to reverse most of the symptom, but if it has past more than 2 or 3 years we often could not reverse the short term memory deficit due to permanent irreversible damage to some of neurons, although we were able to reverse or improve many other abnormalities with significant improvement in other defective functions. Since time factor is very crucial, it is very important to non-invasively screen and detect Alzheimer’s disease in their early stage and treat as soon as possible.
Get full access to this article
View all access options for this article.