August 2007

Updates for August 2007

Key
B=Bacteria D=Disease F=Fungus P=Parasite V=Virus	C=Chemical E=Emotional M=Miasm* T=Toxins
*Multiple letters indicate a combination of issues

Name

Symptom Counter Vibration

Bottles

Contents

Description

ANGMYL

ANGIOMYOLIPOMA

MVB

An arterial/muscle/lipid lump associated with Lymphangioleiomyomatosis and Tuberous Sclerosis.

AST ND 1

ASTROCYTE NUCLEUS DISEASE TYPE 1

MVB

This is one of the versions of Alzheimer's Type 2 Astrocytosis. The disease is a miasmic potential in most people, often producing Astrocytomas (the most common cause of migraines and the most common brain tumor in the world). It is triggered by liver disruptions from hepatitis to alcoholism, etc. The most common cause since 1975 is the introduction of Aspartame into over 5,000 foods in 90 countries. Aspartame blocks glutamine synthetase which causes hepatic encephalopathia (weight gain), ammonia brain toxicity and then this dormant disease. The Astrocytes perpetuate Hepatic Encephalopathia in a Catch 22 of memory loss and weight gain. This version also blocks lecithin, the substance that makes the protective sheath around nerves. The subject often develops tumors, is more prone to other nerve diseases and develops a crab-like flapping of the hands in severe cases.

AST ND 2

ASTROCYTE NUCLEUS DISEASE TYPE 2

MVB

This is one of the versions of Alzheimer's Type 2 Astrocytosis. The disease is a miasmic potential in most people, often producing Astrocytomas (the most common cause of migraines and the most common brain tumor in the world). It is triggered by liver disruptions from hepatitis to alcoholism, etc. The most common cause since 1975 is the introduction of Aspartame into over 5,000 foods in 90 countries. Aspartame blocks glutamine synthetase which causes hepatic encephalopathia (weight gain), ammonia brain toxicity and then this dormant disease. The Astrocytes perpetuate Hepatic Encephalopathia in a Catch 22 of memory loss and weight gain. This version also blocks bile, choline and steroids/hormones in ways that affect gall bladder, stomach and intestines.

FHC 1

FAMILIAL HYPERTROPHIC CARDIOMYOPATHY 1

MVB

FHC is a mutation of the beta cardiac Myosin 2. The symptoms are enlargement of the heart, mild/ occasional tachycardia with exercise and virtually few other signs. The disease is identified as the cause of sudden heart attack in young athletes. All forms of FHC measure to disallow enough blood flow through the heart to nourish lungs, liver and brain.

FHC 2

FAMILIAL HYPERTROPHIC CARDIOMYOPATHY 2

MVB

FHC is a mutation of the beta cardiac Myosin 3. The symptoms are enlargement of the heart, mild/ occasional tachycardia with exercise and virtually few other signs. The disease is identified as the cause of sudden heart attack in young athletes. All forms of FHC measure to disallow enough blood flow through the heart to nourish lungs, liver and brain.

FHC 3

FAMILIAL HYPERTROPHIC CARDIOMYOPATHY 3

MVB

FHC is a mutation of the beta cardiac Myosin 4. The symptoms are enlargement of the heart, mild/ occasional tachycardia with exercise and virtually few other signs. The disease is identified as the cause of sudden heart attack in young athletes. All forms of FHC measure to disallow enough blood flow through the heart to nourish lungs, liver and brain.

FHC 4

FAMILIAL HYPERTROPHIC CARDIOMYOPATHY 4

MVB

FHC is a mutation of the beta cardiac Myosin. The symptoms are enlargement of the heart, mild/ occasional tachycardia with exercise and virtually few other signs. The disease is identified as the cause of sudden heart attack in young athletes. All forms of FHC measure to disallow enough blood flow through the heart to nourish lungs, liver and brain.

FHC 5

FAMILIAL HYPERTROPHIC CARDIOMYOPATHY 5

MVB

HMG CPL

HEMANGIOMA CAPILLARY

MVB

Usually found in birthmarks. First used in Birthmark Type B

LYM PLM

LYMPHANGIOLEIO-MYOMATOSIS

MVB

LAM is called a rare disorder in which abnormal smooth muscle cells grow rapidly in lung and lymph tissue. LAM Smooth muscle cells are considered neoplastic, especially distinctive in lungs and bronchi. It is thought to affect young and middle-aged premenopausal women, but known to occur in men and other age groups. Our testing shows that it is not so discriminating and shows up in men and women at any age. The disease is strongly associated with Angiomyolipomas and Tuberous Sclerosis.

LYNCH 4

MVB

An inherited form of intestinal cancer representing 2-5% of intestinal cancers commonly starting around age 44 and 70% found in the splenic flexure. We believe this a condition of cells because there are "a statistically significant excess" of carcinomas in the endometrium (endometriosis), ovary, stomach, small intestines, hepatobiliary system and transient cell carcinomas of the ureter and renal pelvis. Sebaceous Adenomas and Keratoacanthomas (especially) often accompany the condition. See also Muir-Torre.

LYNCH 6

MVB

LYNCH 8

MVB

MUC COR

MUCOUS CORRECT

MVB

The mucous-specific secretion gland embryo cell dies, causing the gland to dry and become cancerous.

MYO 5A

MYOSIN 5A

MVB

MYO 5A is a neurological/muscle inherited disease that mimics the symptoms of MS, ALS, MD and Stroke (disabled on one side).

MYO 5B

MYOSIN 5B

MVB

Similar to Griscelli Disease, which is characterized by low immune system (weak Thymus) and acute phases of uncontrollable lymphocyte and macrophage activation. It is bone based, inherited and is a little-known disease.

NEC LIV

NECROSING LIVER DISEASE

MVB

A group of miasms that prevent the liver from reconstituting itself and thereby destroys itself with bile, bile blockage and portal vein blockage.

SCR INT

SUCROSE INTOLERANCE

MVB

For the allergy-like reaction to sugar added to flour. It mimics wheat intolerance.

SPLN SM

SPLEEN SUGAROMA

MVB

Exaggeration of Spleen Sugarosis symptoms. Usually with RV Spleeny

SPLN SS

SPLEEN SUGAROSIS

MVB

An unidentified sugar is produced in the spleen. It stimulates adrenals and is one of the causes of light sleepers. It depletes lymph. It weakens bladders causing frequent and/or nighttime urination. There is some connection with histamine in the role of healing cells. This seems to work with Histamine Enzyme Disease. Psychologically it is connected to our desire to serve God, yet feeling we are inadequate to accomplish our tasks. We are often involved in difficult tasks that we subconsciously can't do even though consciously we feel we can do. See also Spleen Sugaroma and RV Spleeny.

SPN T 8/9

SPONDYLOSIS T 8/9

MVB

With Cerebellum Medullary this causes the chin to rest on the chest in a severe forward bend of the neck (where the spondylosis is most obvious in effect).

SPN T4/5/6

SPONDYLOSIS T 4/5/6

MVB

Blocks elasticity and circulation to genitals.

SPN T8

SPONDYLOSIS T8

MVB

Causes low Thyroid (via Ligaments) and hypoactive genitals. T8 is cockeyed.

SUG BON

SUGAR BONE

MVB

The bones make a fundamental sugar: glycerone (dihydroxyacetone) that is carried in the blood and directly catalyzes usage of bile, choline, inositol, lecithin and porphyrins. It is so primary that it resists insulin. When it is infiltrated by phosphorus (because of this disease), the sugar becomes inert, stays in the blood, and does little more than catalyze blood and kidney problems. This phosphorus disease of the bone is therefore responsible for unutilized bile in the liver, gall bladder, nerve weakness because of unused lecithin and weight gain because of unused choline and inisitol. Diabetics with this condition are classified "insulin resistant" or "insulin allergic".

TERROR

The emotion is multiple times fear. It is paralyzing and produces strongly conflicting actions. Whether it comes from this lifetime or before it can so rule your decisions at a deep level that you think life is simply the way you live it (with terror). You may not think of this word, especially when the word terrorist is used so often in society, but think of it as an absolute ruler of your emotions and you might find its hidden presence.