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Organophosphate pesticides make the amino acid, Threonine into a
form of poison instead of a nutrient. Arteries become porous without
this amino acid and leak plasma just as they do in the inherited
disease, Artery Porosity. Leaking plasma and blood nutrients cause
tissue to dry, wrinkle, shrivel and atrophy. Tissue firmness and
engourgability (as in sexual glands) decrease first, followed by
decreases in flexibility and thickness. See also Artery Porosity. |
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As the liver decreases the assimilation of the amino acid, threonine,
the arteries become more porous. Leaking plasma and blood nutrients
cause tissue to dry, wrinkle, shrivel and atrophy. Tissue firmness
and engourgability (as in sexual glands) decrease first, followed by
decreases in flexibility and thickness. See also Artery Deflate. |
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This condition is caused by an inherited Cerebroside Lysis Disease.
The onset is usually slow. Usually the posture stoops first, showing
back weakness. Gradually the nerves to other organs harden, causing
decreases in hearing, taste and sometimes speech. Nerves to the
lungs and trachea harden causing labored breathing and swallowing
for some. For many there is a gradual loss of memory, forgetfulness
and increasing dementia. Hands sometimes shake, muscles can quiver,
legs can become weak, digestion can lead to constipation for lack of
peristalsis. |
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This condition stems from the Ovum/sperm Disease Calcium Glucation.
Because the combined calcium/glucose is seen as an infection,
histocytes attack it. Histocytes are inadequate to dissolve the
combination and therefore 'stick" to it, forming a toxin that blocks
most any function of the body. |
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Usually benign, sometimes malignant stromal, breast tumor that grows
rapidly and tends to recur if not adequately excised. |
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EMBRYO OVUM FACTOR DISEASE |
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The "factor" needed for the Embryo Cell in the thymus to make cells
that can recreate healthy cells is impaired in this disease.
Although this "factor" is seemingly time dependent, it is a physical
reason for longevity and embryo creation. |
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An inherited degenerative disease of the grey matter of nerves. The
sporadic grappling with nerves causes a variety of symptoms from
frequent sore throats, numerous neurological aches and pains in
numerous locations, memory problems, infection susceptibility and
intestinal irregularities. For some it remains sporadic and for
others the sporadic symptoms precede a steady decline in shoulders,
arms and walking ability. The closest similarities are
Creutzfeld-Jakob variations and Neuroacanthocytosis. It is usually
expected in the 3rd and 4th decade, it is seen more mildly presented
thereafter. 10% of the blood usually shows acanthocytosis and there
is decreased striatial glucose metabolism. An MRI usually shows
caudate atrophy and T-2 weighted hyperintensities in the striatum.
There is usually peripheral neuropathy or peripheral dysfunction. |
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Iodine poisoning caused by a Thymus disease that binds iodine to
thymocytes. The disease atrophies the Thymus and starves the
Thyroid. The disease is known to cause excess fluid in the
nose/pharynx, excess saliva, frontal headaches, emaciation
(sometimes covered by excess weight, weakness and skin eruptions (ioderma).
It is a primary block to all sterol activity. Hypothyroid and
hypothymus have many other manifestations. |
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Officially described as a multicentered form of malignant
tumor-like vascular proliferation characterized by blue/red to black
nodules usually on lower limbs that progresses to other areas. There
is an association of this disease as an AID complication although it
is reported as separate and common in Africa and eastern Europe. |
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A second cause of Lymphadema involving a breakdown of venous
sinusoids (the "capillaries of veins") and a specific kind of
lymphoma that follows. |
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A scientifically yet-to-be-proven (6/06) form of scoliosis based on
the gonococcal bacteria. |
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OVUM DISEASE OSSEIN SCLEROSIS |
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This disease originates in the egg when mother has a cell mitosis
disjuncture in her ossien which composes 40% of the protein of the
bone, cartilage and connective tissue. The child has bone and
connective tissue compression that causes stunted growth, dwarfism
(as an extreme) and muscle problems. |
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RETICULOHISTOCYSTOSIS COMPLEX |
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An inherited condition that effects males and females differently.
Usually women develop polyarthritis of the hands and large joints
with nodules on the finger joints or large joints. Nodules have also
been seen in the skin, bone and mucous and synovial membranes.
Sometimes there are ganglia like swellings on the extensor or flexor
surfaces of the wrists. Men develop swelling in the prostate and
liver. Both men and women may develop lypoma like swellings on
muscles. |
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