Nutritional (video)
Microscopy
Nutritional
(video) microscopy of Live & Dried Layered Blood Analysis
is a unique technique used to formulate an appropriate course
of natural health-building and lifestyle principles to
optimize health, prevent disease, and to monitor individual
effectiveness.
Live Blood Analysis and Dried
Layered Blood Analysis are the two
applications that are discussed in the following information.
The two applications are modeled through three viewing
techniques: Phase Contrast & Dark Field (Live Blood), and
Bright Field (Dried Layered Blood), also known as the
Oxidative Stress Test or Mycotoxic / Oxidative Stress Test (M.O.S.T).
The test is different from conventional blood tests ordered
by the physicians because it is a live sample, where the
qualified Analyst is looking for microbial activity, condition
of cells, and anomalies that are not typically ordered in
blood testing using the traditional method. The dried sample
suggests the areas of the body that may be congested, or
holding toxins, impairing proper functionality.
Phase Contrast
Microscopy

An image of fibrin spiculae which should not appear in
live blood at all. It indicates that the balance
between haemostasis and fibrinolysis is too much in
favor of clotting. |
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Around 1930 Professor Fritz Zernike, a Dutch professor in
Physics, discovered phase and amplitude differences between 'zeroth
order' and 'diffracted' light that can be altered to produce
favorable conditions for interference and contrast enhancement
through microscopy. He succeeded in devising a method, now
known as phase contrast microscopy, for making unstained,
phase objects yield contrast images as if they were amplitude
objects.
Phase contrast microscopy was very successful and
ultimately gained widespread application, resulting in
Zernike's award of the prestigious Nobel Prize in physics in
1953. Phase contrast, by "converting" phase
specimens such as living material into amplitude specimens,
allowed the observing scientists to see details in unstained
and/or living objects with a clarity and resolution never
before achieved.
In Nutritional (video) Microscopy this unique technique of
viewing living blood is not a diagnostic procedure for any
specific disease. It is more a screening test to reflect how
one’s dietary and lifestyle habits may be influencing
health, and where appropriate adjustments are necessary within
these areas in order to optimize health and prevent the onset
of disease. Health problems and degenerative conditions can be
prevented with early nutritional intervention, and Phase
Contrast Microscopy can detect many nutritional imbalances and
deficiencies before chemical blood tests can show
abnormalities.
This unique Phase contrast technique of viewing living
blood is different from regular blood analysis because it uses
whole, unaltered blood as opposed to just parts of the blood.
It is unstained and uses higher magnification. The blood which
is viewed directly by the Analyst and the client/volunteer is
alive, and not dead as in conventional chemical microscopic
blood evaluation.

This Phase Contrast image of blood containing colonies
of yeast markers have proven antibody positive for
Candida Albicans (Drs. Majid Ali and Robert Bradford,
Capital University, Washington DC, USA 1994). |
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Techniques of Live Blood Analysis (Phase Contrast &
Dark Field Microscopy) can also view living microbial activity
and their potential degenerative effects within the
bloodstream. The presence of bacteria, fungi or parasitic
forms observed in a live blood screening test is not
diagnostic of an infection with any of these organisms. The
blood and immune system is exposed to these organisms on a
daily basis from the intake of food, municipal tap water, and
the polluted environment of modern life. These organisms, when
they enter the blood stream are generally inactivated by the
immune system’s army of white blood cells and antibodies.
The mere presence of these ‘bugs’ in the blood is not
diagnostic of an infection. For a blood infection to be
present, a great deal more than just microbial activity has to
be observed. Microbial activity within the bloodstream does
however give indications of an acidic compromised biological
terrain suited for the growth and development of such
microbial activity and their excreted exotoxins, and therefore
unsuited for efficient cellular function which requires a
balanced alkaline biochemistry.
Skeptics of Phase Contrast and Dark Field Microscopy
believe that the blood of most breathing, walking and
functioning humans is completely sterile and that viruses,
bacteria, fungi and parasites could not possibly exist in the
bloodstream. They argue that if parasites, candida yeast,
fungi or bacteria were really present in the bloodstream that
the patient should be lying in a hospital bed, perhaps dying
of septic shock. This dogma has been disproved by a great deal
of research done by many scientists around the world,
especially in Germany, Eastern Europe, New Zealand and
countries where natural or drugless forms of medicine are more
accepted.
The list of research papers describing the presence of
viral, bacterial, fungal, and parasitic toxins in the blood of
non-septicemic individuals is voluminous. A growing number of
pathologists (e.g. Dr. A. Ali) and clinicians are recognizing
the importance of using this kind of information in daily
practice of preventive health care.
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This
Phase Contrast image (at left) shows cholesterol in
the bloodstream. While the reading cannot be presented
in mg/dl, one can have a good indication on whether it
is low, moderate or high.
While high
cholesterol can be the result of high intake of
saturated fatty foods, it can also be an indication of
pancreatic deficiency, large intestine dysfunction,
calcium/phosphorus imbalance, malabsorption, liver
disease, and liver dysfunction.
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Dark Field Microscopy
Everybody is familiar with the appearance and visibility of
stars on a cloudless night. They can be seen because of the
contrast between their faint light and the black sky forming a
background. Of course stars shine both night and day; it is
just that they are invisible during the day because the
overwhelming brightness of the sun obscures the faint light
from the stars.
AT
left is a Dark
Field microscopic image of agglutinated erythrocytes (red
blood cells).This is due to several imbalances within the diet
as wells as emotional stressors.
It lowers oxygen to the
tissues reducing cellular efficiency, inhibits efficient
nutrient utilization, hinders the efficient removal of
metabolic waste, and makes the circulatory and lymphatic
systems sluggish.
This same principle is applied in Dark Field Microscopy
which is a unique technique for making unstained objects
visible. Dark Field illumination blocks out of the central
light which normally passes through and around the specimen,
disallowing any light other than oblique rays from every
azimuth to illuminate the specimen on the microscope slide. In
this way a situation is created as described above with the
stars. They become visible against a dark background when lit
obliquely. Objects are now observable using Dark Field
Microscopy that cannot be observed in the Phase Contrast
Microscopy application.
This
Darkfield Microscopic image (at left) show corrugated red
blood cell walls. This is partly due to lipid peroxidation of
their bilayer phospholipid membranes. The white dots on these
poikilocytic RBCs are mycoplasma.
Mycoplasma proliferation is
implicated in many pathologies; mycoplasma feeds on sugars and
produces several forms of sialic acid as metabolic
end-product.
These are pathogens that infect plants, animals and humans.
They are members of the mollicute family, cell-wall deficient
and characterized as a virus-like infectious agent (in-between
a virus and bacteria in complexity). There are hundreds of
different mycoplasma subtypes and numerous isolates within any
given subtype. For example, mycoplasma arthritidis can cause
arthritic conditions, whilst mycoplasma pneumoniae is involved
in respiratory conditions.
Mycoplasmas have a special interaction with the
lymphoreticular system in that they are immuno-modulating
pathogens that can compromise T-lymphocytes. By the time
mycoplasma becomes visible in a live blood sample there is an
urgent need to restore the client’s immune-competence.
Mycoplasma is a single cell bacterium that tends to make
sore, achy muscles, pneumonia, arthritis, and lupus type
symptoms. 60 days of super strong antioxidants inclusive of
Beta-Carotene, Vitamin C, Vitamin E, Selenium, Zinc, Grape
Seed Extract, Sea Kelp, combined with amino acids I-Cysteine,
I-Glutathione will be of great benefit.
Dried Layered Blood

The coagulation in this slide above shows
strong fibrin interconnections and no
disseminated intravascular coagulation typical
of a normal healthy dried layered profile . |
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In Dried Layered Blood Analysis (coagulation
morphology / Bright Field) one examines the result of
the client’s/volunteer’s coagulation cascade. This
is seen through cellular oxidization and degeneration,
which is characterized through the fall out of fibrin
toxic masses, gathered from one droplet of blood and
collected in layers on the slide.
This application of viewing dried suspended blood
samples offers the qualified analyst and client
valuable clues to potential degenerative patterns.
Through the oxidation of the blood cells, and toxins
present in the blood we are able to see characteristic
patterning of an alternative pathway other than the
extrinsic or intrinsic pathways. This allows us to
identify what parts of the body are holding toxins and
therefore functional capacity may be impaired.
This technique may often present profiles that
warrant the analyst making recommendations that the
client visit their primary care physician for
additional tests.
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| Coagulation in this
slide shows a profound absence of fibrin network which
reflects an amino acid deficiency caused either by an
ingestion, digestion or assimilation problem |
The above slide is a
profile typical of individuals with chronic digestive
irregularities and bowel toxicity. |
This profile above is
indicative of mental / emotional stress which
indicates potential effects on the functional
efficiency of the adrenal glands. |
Since the systems within the human body are all
interconnected, functioning as a whole, then by viewing the
living elements of human blood using 'Phase Contrast,' 'Dark
Field' modalities, one can observe biological imbalances that
can have implications on the functional efficiency of various
biological systems and the organs that comprise the system. By
using the 'Bright Field' modality (dry layered blood) of
analysis, one can gain insight into degenerative patterns and
indications in various areas of the body.
Nutritional (video)
Microscopy Can Show:
• The
conditions of the red blood cells, white blood cells and
platelets, and their implications on health.
• Nutritional
deficiencies and indications of inefficient absorption and
assimilation.
• Features
associated with blood sugar imbalances.
• Features
associated with crystalline forms such as cholesterol,
triglycerides, uric acid, protoplast.
• Free radical
activity and cellular oxidation.
• The presence
of microbial activity such as bacteria, yeast, parasites,
fungi.
• Levels of
toxicity and internal pollution.
• Organ
stresses or weaknesses such as: pancreas, liver, kidneys,
prostate, heart, breast, reproductive.
• Features and
early warning signs associated with degenerative conditions.
Copyright © 2001 InnerLife Wellness Center
REFERENCES
Ali, Majid. RDA: Rats, Drugs and Assumptions. Denville, New
Jersey:Life Span Press, 1996 p.424-462.
Martin, Jeanne Marie and Rona, Zoltan P. The Complete
Candida Yeast Guidebook. Rocklin, California:Prima Books,
1996.
Rogers, Sherry A. Finally Healing the Immune System.
Macrobiotics Today. September/October 1995; pp. 16-20.
Rona, Zoltan P. and Martin, Jeanne Marie. Return to the Joy
of Health, Vancouver: Alive Books, 1995.
Rona, Zoltan P. Childhood Illness and The Allergy
Connection. Rocklin, California:Prima Books, 1996.
Simpson, L.O. Red cell shape changes following trigger
finger fatigue in subjects with chronic tiredness and healthy
controls. NZ Med. J. 1993; 106:104-7.
Simpson, L.O. Nondiscocytic erythrocytes in myalgic
encephalomyelitis. NZ Med. J. 1989; 102: 126-7.
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