SYNCROMETER® SCIENCE LABORATORY MANUAL

Using The Zapper

1. Wrap handholds in one layer of wet paper towel before using. Grasp securely and turn the
switch on to zap.
2. Zap for seven minutes, let go of the handholds, turn off the zapper, and rest for twenty
minutes. Then seven minutes on, twenty minutes rest, and a final seven minutes on.
Trying the zapper on an illness to see “if it works” is not useful. Your symptoms may be due
to a non-parasite. Or you may reinfect within hours of zapping. The best way to test your device is
to find a few invaders that you currently have (Exp. 13). This gives you a starting point. Then zap
yourself. After the triple zapping, none of these invaders should be present. If they do survive,
especially the larger ones like Fasciola flukes, they are undoubtedly saturated by an insulating
substance such as PCBs, freon or benzene. For this reason, plate-zapping was developed.

Syncrometer® Based Plate-Zapping

By passing the zapper current through a capacitor plate in the same manner as the
Syncrometer® current, a similar effect can be observed. The item placed on the plate directs or
invites the current; in fact, nothing else will be zapped. My interpretation is that the capacitor plate
on the resonance box has a “standing wave” relationship to an identical capacitance in your body,
making the resistance between them essentially zero. Nearly all the current will go to this location
in your body. The standing wave relationship can be seen for the Syncrometer® where the addition
of 2pF capacitance to the plate destroys resonance, but the further addition of two microhenry
inductance restores it again.

The Plate-Zapper
The plate for the plate-zapper can be provided by the plate-box as is used for the
Syncrometer®. However, other plates as well as homemade plates are equally effective. The
Syncrometer® plate-box has two metal squares one of which is normally connected to the
Syncrometer® circuit. The other square can be added to the first one by means of a shorting switch.
For plate-zapping, the connecting cable to the Syncrometer® is removed and replaced by a
cable to the zapper. The two plates are kept permanently connected (shorted).
The zapper itself has two output terminals, where leads are to be attached that go to your
body via conductors like copper pipes or wristbands. Identify the “hot” output terminal with an
oscilloscope or voltmeter; you may need to take it to an electronics shop for this small but crucial
bit of information (or ask the manufacturer). From this terminal, connect a lead to any one of the
two plates. The other “cold” terminal will be connected as usual, straightaway to your copper pipe
or wristband. The same plates as are connected to the zapper are next connected to the other copper
pipe electrode or wristband.

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Note that no ground connection is used for the plates. They simply attach or “T” into the hot
lead (Positive) on its way to you, the electrode holder.

Homemade Plate-Zapper
You can build your own plate-zapper using
sardine can lids (not other cans). After careful
washing and unrolling to make the surface as flat as
possible, you can mount them on the lids of empty
vitamin bottles (the kind with plastic caps). Make a
nail hole near the center of each lid and bottle cap.
Find sheet metal screws to fit the holes. Tighten the
can-plates to the lids just enough to be still movable
by finger touch.
You may use your homemade zapper in
conjunction with your plate arrangement. Use an
alligator clip lead to connect the hot (Positive) side Homemade plate-zapper
of your zapper to one of the can lid plates, being 2 sardine can lids overlap slightly and are
careful not to disturb its flatness. Connect another held together tightly by the grip of an
alligator clip lead from the same plate, back to your alligator clip lead. Lead goes to positive
foot, hand or skin location. You may use copper output from zapper. Another lead from
pipes, aluminum or copper plates to contact your lids goes to a foot electrode (copper pipe,
body. in this case). The second (negative) output
If using two can lids they must be very securely from zapper goes to other foot.
connected at all times, such as by an alligator clip.

Exp. 98 Plate-Zapper Directs

Current To Location
Indicated On Plate
Purpose: To observe the specificity of a zapper.
current when a capacitor plate is used in line with the
“hot” lead from the zapper. To show that the organ sample
and pathogen-invaders that are placed on the plate are Plate-zapper
specifically involved, and none other. has location to be zapped on one (left)
Materials: A regular zapper or homemade zapper, a plate. Bottles or slides must touch each
plate box with two 3½inch square metal plates, as used other here to make a single location out of
with a Syncrometer®. If using a frequency generator it must them. Emerging pathogens are placed on
other (right) plate, as well as targeted
be set up to produce a square wave at 30 KHz with
pathogens. Here entities do not touch each
other.

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the amplitude and offset controls set so that all output is Positive. No tiny spike of Negative voltage
can be allowed since this assists pathogens instead of killing them. Such settings must be
determined by an electronics-skilled person and must never be left to chance.
Note: I refer to zappers made for Self Health Resource Center; I have not used others in these
experiments.
Methods: 1. Find which of the two output terminals on the zapper is the “hot” (Positive)
side. Connect this to one of the box plates. An alligator clip lead will do. You may use other kinds
of leads and even include your wrist strap (the conductive part must be located) to make the
connection to the plate.
2. Set the switches on the plate box so the two plates are combined (shorted). Keep these
switches permanently in ON position to avoid errors. Also connect these plates to the electrode you
will hold or attach to yourself. If you are using a wristband, connect the plates to your wristband.
Notice: The plates are simply attached in a T-formation to the circuit; there is no ground or separate
pathway away from the plate.
3. Find an organ that has several pathogens or parasites, or choose an organ where you have
pain and for which you have a specimen. The pain will be due to Streptococcus pneumoniae.
Search for these and others in nearby organs as well; they should be Positive for this experiment.
4. Place the organ slide (only one) and pathogen slides (more than one) on any plate. For eggs
and stages of parasites use only 3 slides. For bacteria or viruses, use up to 6. All these varieties
can be used together in a single zapping, making 6 to 8 items on your plates but including only one
location. Deliberately leave a few pathogens, that you found Positive earlier, off the plates.
5. Zap for twenty minutes straight without intermission.
6. Test again for the pathogens at the same organs as above. Note: Only those pathogens put
on the plate and only the organ put on the plate will be cleared. Neighboring tissues and other
pathogens are unaffected. The pathogens deliberately left off the plate will still be there.

Exp. 99 Plate-Zapping Large Flukes

Purpose: To observe the outcome of plate-zapping the large flukes, Fasciolopsis and
Fasciola.
Materials: Slides or specimens of Fasciolopsis (Human Intestinal Fluke) and Fasciola
(Sheep liver fluke); slides of fungus varieties: Potato Ring Rot, Cabbage Black, Aspergillus (any
variety), Penicillium, (any variety), Chaetomium, homemade specimen of bread yeast or a slide of
Saccharomyces cerevisiae, homemade specimen of Sorghum mold.
To make a bread yeast specimen, use dry yeast from a package or a piece of yeast cake.
To make a Sorghum mold specimen, purchase several varieties of syrup and molasses at a
health food store. Make separate specimens, labeling each and adding an equal amount of water.
Methods: Find several locations, such as duodenum or colon where Fasciolopsis or
Fasciola adults test Positive. If you are particularly healthy and cannot locate any in your digestive
organs, search at bile duct, gallbladder, and pancreas. Also search at organs that are suffering pain
or dysfunction. Arrange a zapper so the hot lead passes through (is attached to) a flat metal plate
such as a Syncrometer® plate. You may use alligator clips directly clipped to one plate. Attach
another alligator clip to the same plate and lead it to the handhold or wrist strap. You

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may alternatively lead it to a metal pipe or plate for a foot contact. The ground (cold) lead from the
zapper goes to the other hand or foot.
Place slides of Fasciolopsis and Fasciola on the plate. Place the organ slide on the same
plate or on the neighboring plate. They are connected so they act as one anyway.
Zap yourself for seven minutes. After a five-minute rest, test yourself for Fasciolopsis and
Fasciola at the organ site zapped and other organs. Also test yourself for parasites and bacteria
found at that organ earlier but not placed on the plate.
Observations: Only the parasites and organ placed on the plate are affected by the zapping.
Repeat testing later in the day. Include tests for the fungi specimens. Note that several hours
later, Fasciolopsis and Fasciola are still gone but Sorghum mold is now present.

Exp. 100 Digestive Enzymes Get Rid Of Dead

Flukes
Purpose: To observe the benefit of taking digestive enzymes after killing the large flukes,
Fasciolopsis and Fasciola.
Materials: Digestive enzyme mixtures in bulk or in capsules, set of fungus slides used in
Exp. 99.
Methods: Repeat Exp. 99, using a new organ and a Fasciolopsis or Fasciola slide. As soon
as the seven-minute zap is completed, swallow 10 or 15 capsules of mixed digestive enzymes or
pancreatin and lipase. Several hours later, test for fungus varieties.
Observations: Sorghum mold does not develop now, nor other fungi.
Note: Which digestive enzyme is most efficient has not yet been determined. Perhaps you
could obtain them singly and repeat the experiment many times to clarify this.

Exp. 101 Zapped Fungus Releases Cobalt

Purpose: To kill the fungus, Sorghum mold, and observe the appearance of elemental cobalt
in its place.
Materials: Tissue slides, parasite slides, bacteria and virus slides, fungi specimens or
slides, metal test substances, including copper, cobalt, vanadium, germanium, selenium, chromium
(valences 3 and 6), nickel; Bakers’ yeast, Gaffkya bacteria.
Part A. Methods: Zap Fasciola at an organ for seven minutes. Wait fifteen to thirty minutes
until Sorghum mold can be detected there. Test also for the series of metal elements and other fungi.
There will be no metals yet. Then zap the Sorghum mold by placing it on the zapper plate along
with the same organ. After seven minutes rest briefly (five to fifteen minutes) and test again for
other fungi and the metal series.
Results: Cobalt is now present in copious amounts. Sorghum mold will be absent. Yeast, that
is plain Bakers’ yeast, may now be present also.
Note: This may be a somewhat “dirty” experiment in that there are numerous fungus varieties
and numerous other parasites still at that location. You may need to repeat this experiment many
times at other locations to convince yourself that killing Fasciolopsis and

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Fasciola results in Sorghum mold proliferation. This, when killed, leaves a residue of highly toxic
cobalt. Cobalt is the main toxin in heart disease and a common denominator in tumors.
Part B. Sorghum mold growing in the body appears to be accompanied by a bacterium,
Gaffkya, coming and going right along with Sorghum mold. Find a location where the mold and
Gaffkya are Positive but cobalt Negative. Zap only one of them to see which one really releases the
cobalt.

Exp. 102 Paragonimus Releases Pneumocystis

Purpose: To observe the after effect of killing Paragonimus flukes and the benefit of taking
digestive enzymes.
Introduction: Paragonimus flukes are somewhat less numerous than Fasciolopsis and
Fasciola. Since they are smaller it takes a keen eye to spot them. It also takes a watery stool to
allow them to be seen in the commode. They are 1/8” to 3/16” long as seen, dead in the commode.
Like the two larger flukes they burst apart in the toilet water, probably for the reason that they are
accustomed to the 1% salt solution of your body. After bursting, their egg strings are on the outside
sticking closely to them at first.
The easiest identifier for Paragonimus flukes is the presence of three dots, easily seen with
the naked eye; two are red, the other one is brown. Under a binocular microscope you can see that
the two red “dots” are actually round suckers, one at the end, the other, about half way down. The
brown dot is near the edge, across from the middle dot. I am not sure what organ it represents.
Materials: Set of fungi slides including Chaetomium and Bakers’ yeast, Pneumocystis
carinii, organ slides, and metal test substances.
Methods: After locating a Paragonimus (it prefers the lungs), but not Fasciolopsis or
Fasciola, at a tissue, prepare to zap it. Test for fungi and metals also. After zapping for seven
minutes, retest. There will be no new fungus or metal yet. After several hours test again.
Results: Chaetomium, fungus with cellulose-digesting capability, according to biological
supply companies is the fungus that I observe inherits dead Paragonimus carcasses.
Immediately after zapping Paragonimus, test for Pneumocystis carinii, also classified as a
fungus. It travels quickly to the lungs and brain. In large enough numbers, it causes dizziness. The
essential oil, Myrrh, can kill Pneumocystis. Use 6 to 10 drops in a single dose, several times a day.
Or put Pneumocystis on the plate, for zapping next.
Again, digestive enzymes in a large amount, taken immediately after zapping, can prevent
Chaetomium fungus from taking over. But this does not prevent Pneumocystis from emerging.
Pneumocystis does not threaten the cancer patient or others unless lung disease is already present
or AIDS is progressing.

Exp. 103 Aspergillus and Penicillium Fungus

Grows Next
Part A. Purpose: To observe the growth of Aspergillus and Penicillium fungi as a sequel to
Sorghum mold after it is killed by zapping and it releases elemental (metallic) cobalt.

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Materials: Fungi set, heavy metal set.

Methods: Observe the presence of Sorghum mold at an organ tissue for several days (or
months). Test for other fungi at this location and for heavy metals. If possible find a location that
has no elemental copper, cobalt, vanadium, germanium, chromium or nickel. Then zap the fungus
using an ordinary (without a plate) zapper. Retest a few hours later.
Results: Sorghum is now gone but Aspergillus and Penicillium are now present. The element
cobalt is now present, too.
Conclusions: The only organic form of cobalt known is in vitamin B12. Evidently, the killing
of Sorghum mold, or perhaps Gaffkya, results in the destruction of its vitamin B12, releasing cobalt.
Elemental cobalt, besides being highly toxic to the heart, inhibits enzymes involved in acetyl
coenzyme A utilization. Since acetyl CoA plays a central role in metabolism, cobalt toxicity is
easily identified; the LDH in the blood is lowered to below normal levels, showing that not even
lactic, (implicating pyruvic) acid is being made, and chronic fatigue sets in.
Part B. Obtain a saliva sample from a person who states he or she has chronic fatigue (they
usually understate the symptoms). Or test this person directly. You will find copious amounts of
cobalt in many organs, including muscles.

Exp. 104 Growth Of Potato and Cabbage Fungus

Is Next
Purpose: To observe the growth of Potato Ring Rot and Cabbage Black fungus after killing
Aspergillus and Penicillium species.
Materials: Fungi set, heavy metal set.
Methods: Find an organ that has only Aspergillus and Penicillium varieties of fungus and is
Negative for copper. Zap with these two fungi on the plate.
Results: Aspergillus and Penicillium are now gone but Potato Ring Rot or Cabbage Black
fungus or other food fungus is now present. Elemental copper is now present.
Note: Copper in metal form can be identified under the skin, along with Aspergillus and
Penicillium in the brown patches commonly seen there. These are evidently locations of continued
fungus growth and production of copper metal.

Exp. 105 Killing A Variety Of Food-Related Fungi

Part A. Purpose: To observe the effect of killing a variety of food-related fungi and see the
supremacy of bread yeast, Saccharomyces. To observe the origin of elemental (toxic) vanadium,
germanium and chromium.
Materials: Fungi set, zearalenone (mycotoxin), organ set, benzene, mixed blue green algae
slide, Bakers’ yeast, foods as listed below to provide fungus sample.
Methods: Locate an organ that is growing Potato Ring Rot fungus or other food-related
fungus (cheeses, coffee, vegetables, fermented amino acids, and other fermented foods each contain
their predominant mold, which grows in us when immunity fails.) but not Sorghum mold or
Penicillium or Aspergillus. Test also for zearalenone and heavy metals. Note that the

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mycotoxin zearalenone is present wherever Potato Ring Rot is found, and wherever there is
zearalenone there is benzene. So we see for the first time a perfectly “natural” route to immune
deficiency. Zap with Potato Ring Rot on the plate.
Results: The Potato Ring Rot is now gone. In its place is Baker’s yeast and other food fungi.
Zap the remaining fungi. Now we see many more yeast varieties and blue green algae! And we also
see elemental vanadium, germanium and chromium (both valencies 3 and 6).
Conclusions: Although the large flukes, Fasciolopsis and Fasciola are easily killed, they
leave behind dead matter that immediately invites fungal invasion, each with its characteristic
mycotoxin product and characteristic heavy metal release upon its death.
Part B. After killing the flukes at a location in the digestive tract, test for fungi.
Note: The fungi do not develop now.
Conclusions: Evidently, the dead matter created by killing parasites in the digestive tract can
be disposed of and this prevents the growth of numerous highly toxic fungus varieties with their
own heavy metal releases. But when dead matter occurs in an organ that does not open into the
digestive tract, fungi and yeasts consume it in an orderly manner.

Exp. 106 Dare To Kill Yeast

Discussion: We are familiar with the yeast, Candida albicans, growing in our bodies. It is
visible as a whitish scum on the tongue or as a discharge from genital organs. Candida grows in
two ways, by budding and by growing long threads that divide up into individual cells. These long
threads, called hyphae, produce tiny roots that can penetrate our cells without destroying them.
These rootlets are merely pushing their way into our cells to drink our nutrients. Because they grow
into our cells they are largely protected from things like iodine or antifungals that we might put on
our cell surfaces to kill them.
Yeasts belong to the mold and fungus family of life forms. They are plant-like in having hard
cell walls that give them unchangeable shapes. Yet they are animal-like in making chemicals in
their metabolism that are related to cholesterol! Perhaps their “plant-animal” features make them
able to parasitize us. Perhaps yeasts and fungi were some of the first parasites we had, since the
beta glucans found in yeast cell walls (and mushrooms) are the very substances used by our white
blood cells to communicate to others that they have caught an intruder and they must mobilize
themselves to attack. Yeast and mold spores are so abundant in nature that any dust sample taken
inside your home, or outside, has many varieties of them. This makes it possible to set out a dish of
starch solution or fruit and after a week or so turn them into bread (sourdough) or an alcoholic
beverage. (It must be properly attended).
The Syncrometer® detects two kinds of yeast living in both places; the dust on your
windowsill and inside your body. They are common Bakers’ Yeast, Saccharomyces cerevisiae,
and Fission yeast, Schizosaccharomyces octosporus (Schizoyeast, for short). Phoma, another
common fungus is found in both places, too.
All three are found everywhere. In advanced cancer patients they have begun to take over the
previous fungi and are now freely swimming in the blood to any location. They will begin to
consume the body as long as there is sugar and nitrogen to be consumed. The blood and other body
fluids have plenty of both. Some fungi have an enzyme, urease, with which to attack our ready-made
urea. They turn it back to ammonia from which we made it (with our urea synthesis

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cycle). Ammonia is toxic to all our cells and, in fact, its formation becomes our terminal event.
Clinically, it is interpreted as liver and kidney failure. But the Syncrometer® finds ammonia to be
the cause of their failure (not the result). Although their presence has sinister meaning and brings
fatal consequences, that is not all!
These two yeasts are themselves infected! While they are living in us they become infected
with two major oncoviruses. Bakers’ yeast sampled from your windowsill does not harbor them,
but the same yeast detected in your body carries RAS, a piece of oncovirus. Moreover, the Bakers’
yeast purchased in packages or cakes at a market is infected with RAS, as is most of the bread on
the supermarket shelves.
Fission yeast taken from your windowsill does not harbor them either. But the same
Schizosaccharomyces detected in your body harbors JUN, even more oncogenic than RAS. JUN,
too, is found in packaged yeast and the soft breads on grocery shelves. Phoma brings a deadly
mycotoxin, phomopsin.
Purpose: To observe the presence of common Bakers’ yeast, Schizoyeast and Phoma in
house dust, bread and the body.
Materials: Slides of Saccharomyces cerevisiae, Schizosaccharomyces octosporus, Phoma
lingam; phomopsin; samples of dust from a top window ledge of several homes, a slice of bread
from several popular brands, tissue slides, fungi set, outside dust from a window ledge, RAS, JUN
oncogenes.
Methods: Test the dust samples and breads, adding water to each, for the yeast and mold
varieties in your possession. Then culture your dust samples with a pinch of sugar and added water.
Test again in a few days after storing in a warm place. Test for RAS and JUN. They are absent
although the yeasts and Phoma are present.
Then test your own blood and tissues for these yeasts and oncogenes. You may find them in
the stomach wall, intestinal wall, a wart or a sick organ. You may find them in a tumor along with
other fungi. Here you will also find RAS, JUN and phomopsin in copious amount. In fact, they have
spread to many other body organs.
Conclusion: Ordinary yeasts and molds can get a foothold in our bodies growing as if we
were their regular turf. Which one grows seems to depend on the heavy metal available at a site of
dead refuse.

Exp. 107 RAS and JUN In Grocery Store Packaged

Yeast
Purpose: To find the oncogenes RAS and JUN in grocery store packages of dry yeast.
Materials: RAS, JUN, cMyc, cFos, (probes), dry yeast package or bulk supply from health
food store, radio clock.
Methods: Search for these peptide bits of genes in a dry sample of yeast. You may find them
Negative. Then search at an exact time from :50 to :10, meaning 10 seconds before to 10 seconds
after :00 time (number 12 on the clock), using a radio clock. If you do not have one, search
repeatedly, at least once every two seconds, in order not to miss its two-second resonance time in
every minute. (You may call a Radio Shack for the exact radio time and set your clock.)

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Add warm water and sugar, keeping it covered, for about five minutes. You should see tiny
bubbles. Test again. Now RAS and JUN will be Positive, but not cMyc or cFos. As the yeast
grows, much more RAS and JUN are produced, as you will see.
Note: cFos comes from Fasciola flukes. The true origin of cMyc is not known, although it is
seen in all chickens in the marketplace.

Exp. 108 Our True Source Of RAS and JUN May

Be Bread
Purpose: To find the true source of RAS and JUN.
Materials: A dust sample containing budding yeast; Fission yeast, Phoma, RAS, JUN,
Bakers’ yeast, test samples.
Methods: Search for RAS and JUN in several Bakers’ yeast samples that you have set to
grow in warm sugar water. Note: Not all Bakers’ yeast samples have RAS and JUN. Not even all
of them have RAS alone. Test them for the presence of Saccharomyces, Schizosaccharomyces and
Phoma. Compare your findings with mine that JUN does not occur in regular Bakers’ yeast but does
occur where there is Fission yeast. And RAS occurs in Bakers’ yeast, not Fission yeast. I
concluded that Fission yeast is a common contaminant of regular Bakers’ yeast, that they are often
infected with oncoviruses, giving us both RAS and JUN in underbaked bread.

Exp. 109 Bakers’ Yeast and Clostridium Bacteria

Release Chromium and Nickel
Purpose: To observe the association of RAS infected yeast with clostridium varieties and the
appearance of the urease enzyme.
Materials: Infected and non-infected Bakers’ yeast specimens, urease, metal set, bacteria set,
RAS oncogene. To make a non-infected yeast specimen: Place about 1 tsp. ordinary dry yeast or a
small piece of yeast cake under a full spectrum lamp, as close as possible to the bulb. Leave it
there for thirty minutes. This will kill the RAS oncovirus, even in the chromosomes.
Methods: Part 1. Locate a tissue where only Bakers’ yeast is present and the clostridium
varieties as well as chromium are absent. Test for urease, it will be absent. Zap the yeast with a
regular (non-plate) zapper. Note that yeast is now absent but chromium is present. Elemental
chromium is possibly derived from glucose tolerance factor, the only organic molecule that
contains it, to my knowledge.
Part 2. Next, locate a tissue where Bakers’ yeast is present and clostridium varieties are also
present, as in a tumor. Test for urease; it will be Positive. Evidently the clostridium bacteria make
the enzyme urease. Urease contains nickel in organic form. Zap yourself with your regular (no
plate) zapper. Clostridium and Bakers’ yeast will be gone if retested immediately afterwards (and
if PCBs are not present to inhibit the current from penetrating).
Results: Urease will be Negative now, while nickel is Positive. Evidently nickel is released
from urease, which is no longer being produced, since Clostridium is dead. Test for infected and

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non-infected yeast; they will be gone. Test for RAS, it will be Positive. Evidently the RAS
oncovirus was left behind, quite alive and proliferative, although the yeast was killed.
Part 3. Search again for yeast and clostridium the next day. Note: They will be back and
cannot be eradicated by simple (non-plate) zapping. The availability of nickel and chromium may
facilitate their return.

Exp. 110 Dare To Kill Yeasts Again

Purpose: To observe the effect of killing yeasts.
Materials: Budding yeast, Fission yeast, Phoma, tissue set, metal set (copper, cobalt,
vanadium, germanium, chromium, nickel), fungi set, slide of mixed blue green algae which includes
Anabaena, Anacystis, Achlya; set of clostridium varieties.
Methods: Find a tissue harboring only these yeasts and Phoma as in quite advanced cancer.
Test for metals. There should be none (they are all in use by these invaders). Then kill the yeasts by
plate-zapping with the organ and yeast specimens on the plate. After several hours test for metals,
fungi, yeasts, blue green algae mixture, and clostridium.
Results: Only blue green algae and Phoma are now present. The metal, nickel, may be
present also. Zap these again and retest after several hours. Only clostridium and nickel remain. But
after several hours, Anacystis, Anabaena, Achlya, or Phoma return again. The cycle keeps
repeating.
Conclusions: The picture is not perfectly clear. Not enough testing has been done. But it
would seem wise to chelate away the nickel to stop an ongoing cycle of yeast, fungus and
clostridium living on each others remains, enabled by the toxic element nickel, which they build
into their enzyme urease, so they can continue to live on the proteins of each other and your body.
Even better than chelating out the nickel (with EDTA by IV administration)) would be
reestablishing your body’s immunity at this site so the white blood cells could remove yeasts,
clostridium, Phoma, blue green algae, and nickel altogether, and take them to the bladder.

Exp. 111 Only Four Immune Problems Challenge

Us
Purpose: To observe the immune problems at locations where nickel is found in the body.
Materials: White blood cell slide, tissue slide set, metal set, ferritin, lanthanide set, benzene,
PCB sample.
Making your own PCB sample: Since at least half of the cooking oils in the supermarket or
health food store contain PCBs, as well as over half of soaps, shampoos, lotions, and deodorants,
you can increase your chances of having a sample of PCB by combining them.
You may also purchase or make a copy of PCBs in a small test bottle of water as described in
Exp. 96.
Methods: Find a location in the body where yeasts are growing and where nickel is present.
Search here for a possible immune problem. Using the white blood cell slide, together with the
location (not touching), search for nickel and yeast in the WBCs. If Negative, search for ferritin.

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Search for lanthanides (including thulium and holmium) in the tissue. They will not be in the WBCs.
Search for benzene. Finally search for PCBs. These 4 substances are the only true immune blockers
I have found. Recall that ferritin on WBCs is due to presence of asbestos.
Conclusion: To reclaim the health of this tissue for your body, you will need to remove all 4
immune blockers. You can already remove 3: ferritin (enzymes and levamisole), lanthanides
(magnet), benzene (vitamin B2 and magnesium). But PCB removal requires special supplements and
special zapping (see Exp. 122).

Exp. 112 Egg Release From Large Flukes After

Herbal Treatment
Purpose: To observe the release of eggs after killing Fasciolopsis and Fasciola using herbs
alone.
Materials: Green black walnut tincture or freeze-dried capsules; cloves (freshly ground),
wormwood; Fasciolopsis adult and developmental stages, Fasciola adult and developmental
stages; tissue slides, including blood, lymph vessel with valve, vein with valve, connective tissue,
skin, capillary.
Methods: Part 1. Search for several locations where parasites reside. Take the herbal
potions as described in previous books; 1/2 hour later (or less) retest for parasites at organs where
they were previously seen and in blood.
Results: For most locations they are all gone. However, the blood will contain eggs and
early developmental stages, especially miracidia. (The order is eggs à miracidia à redia à
cercaria à metacercaria à adults.)
Part 2. Search for locations where parasites reside; if hard to find search in lymph vessel
valves of the skin or skin-connective tissue. Arrange all these tissue specimens on the plate so they
are touching each other, but not overlapping. For example, skin slide and lymph vessel slide
touching along an edge. Also test at skin touching connective tissue-touching lymph vessel with
valve. Fasciola and its stages can often be found here when nowhere else. Fasciola metacercaria
are most often found at capillaries. Take 10 tsp. green black walnut tincture; no other herbs.
Results: All parasites and stages will be gone; none will be in the blood. Nor will yeasts or
Sorghum mold be present at first.
Comments: The exact amount of herbs needed to get a complete kill so no eggs are dispersed
and no fungus spores survive has not been determined yet. It may depend on the degree of
infestation. For this reason it seems wise to always include zapping as part of a deparasitizing
program. Even a classical (non-plate) zap clears the blood.

Exp. 113 Clearing Blood Of Parasites

Purpose: To observe clearing the blood of parasite stages electrically.
Materials: Slides of parasites eggs and stages; a blood slide.
Methods: Find parasite eggs and larval stages in your blood.

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Arrange the zapper to omit the plate; namely to zap in the classical way. Zap for seven
minutes. Retest immediately and later. Note that the blood is immediately cleared but within hours
parasite eggs appear again, evidently being released from a dying parasite far away. Within hours
new developmental stages are seen in the blood. They can be followed to various tissues where
they continue their development.
Next, arrange the zapper to include the plate with the blood slide on it. Zap for seven minutes.
The blood is immediately cleared as before. But eggs will return again in heavily infested persons
or PCB-saturated persons.
Conclusions: Regular zapping is as effective as plate-assisted zapping when trying to clear
the blood. But in heavily infested persons or when PCBs are present, a single zapping is not
adequate.
We will soon see that killing parasites by zapping (of either kind) does not allow dispersion
of eggs afterward by means of the blood, if done repeatedly.
For this reason it seems advisable for heavily infested persons: 1. To kill parasites
electrically and to zap continuously (all day) until the blood stays clear. 2. To take the parasite-
killing herbs only while zapping (in the regular way or in the plate-assisted way).

Exp. 114 Plate Versus Regular Zapping

Purpose: To compare effectiveness of plate-directed zapping with regular classical zapping.
Materials: Parasite set, fungi set, heavy metals, zapper plate attachment, tissue set.
Methods: Attach the zapper plate to your zapper. Check all switches to be sure they are in
correct position. Place a slide of the organ to be zapped on the plate (since plates are electrically
connected, it does not matter which one is used). Place Fasciolopsis and Fasciola slides on the
plates. Place samples of Sorghum mold, Bakers’ yeast, Penicillium, Aspergillus, and Potato Ring
Rot on the plate. Zap for twenty minutes not just seven. Be sure to use a fresh battery, with a voltage
of at least 9.4 volts.
Results: All the items on the plate should be absent at the organ that was placed on the plate.
No parasite eggs should appear in the blood later. No heavy metals or new fungus should be left
behind or appear later. In other words, plate-zapping kills more completely than classical zapping.
Recall that a new fungus and a metal is always seen after classical zapping.
Note: If some items did not get zapped, check battery voltage with a voltmeter. If battery
voltage was not low, you may be “non conductive” due to PCBs in your body. Search for PCBs in
your cooking oil, soap, shampoo and lotions.

Exp. 115 Zapping Two Organs On The Plate Fails

Purpose: To observe the effect of placing two organs on the plate for zapping.
Materials: Parasite set, tissue set.
Methods: Find parasites at two tissues. Place both tissues and the parasites to be killed on
the plate as usual for plate-zapping. Zap twenty minutes.

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Results: Only one tissue will get zapped. Try positioning the two tissues differently but not
touching, on the plate, zapping for a longer time period, using a higher battery voltage (within the
limits of your device).
Conclusion: I interpret this to mean that the current goes preferentially to one organ, it is not
divided equally. Tissues placed on the plate appear “in parallel” in the circuit. When two or three
bottles or slides are needed to describe a location, they must touch each other to create a single
location that does not divide the current.

Exp. 116 Zapping A Tumor

Purpose: To specifically zap a tumor.
Materials: Tissue set, parasite set, fungi set, tricalcium phosphate test bottle or slide.
Methods: Place the tissue that has the tumor on the plate. This will not zap the tumor, only the
surrounding tissue. Place the tricalcium phosphate on the plate with the tissue but not touching it.
The current will now zap the tumor, and not the tissue that bears it. Zap the tumor for twenty
minutes. Remove the tricalcium phosphate and test for parasites (you are now in the surrounding
tissue). They will be there since they were not zapped. Replace the tricalcium phosphate and test
for parasites (they will be absent since these were zapped). Remember to place emerging
pathogens on the other plate (see Exp. 118).
Discussion: Tricalcium phosphate identifies nearly all tumors. This is due, no doubt, to the
involvement of the “calcium cascade” whereby some agent such as a lanthanide has caused internal
release of bound calcium. This in turn stimulates calmodulin, adenylate cyclase, cAMP, and protein
kinase C that triggers cell division. For this reason, tricalcium phosphate serves as a marker for
detecting and for zapping a tumor (see Exp. 76). Zapping a tumor and opening it are different
processes, though. And you cannot test objectively that you have reached the tumor with the zapper
unless you can see some change there. Search the surrounding tissue for the things that were
previously in the tumor. If they are there, it is electrical evidence that the tumor is draining. The
only visible evidence would be a scan.

Exp. 117 Plate-Zapping Tapeworms Ineffective

Purpose: To observe the ineffectiveness of plate-zapping tapeworm stages.
Materials: Slides of Moniezia stages, Hymenolepis stages, Taenia stages, Echinococcus
stages, others.
Methods: Plate-zap as usual at a location where you detected tapeworm larvae.
Results: Nearly all the tapeworm stage parasites are left intact.
Comments: What might be an explanation for this failure? Too low voltage? Do tapeworms
require higher currents? Must they be specified by frequency? Is their location nonconductive? We
will try to use these theories next.

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Exp. 118 Double-Zapping: Sine Wave and Square

Wave Together
Discussion: A sine wave added to a square wave, both Positive offset, can kill tapeworms
and their stages completely. Is it merely due to a higher total voltage, using a number of
frequencies, or some other aspect of the double wave? Only more research can clarify this.
Purpose: To observe the greater effectiveness of a sine wave and square wave combined,
both Positive offset, in killing tapeworm stages, flukes, fungus, bacteria and viruses all together.
Materials: A zapper arranged to operate through a plate, as in the plate-zapper, a frequency
generator that has been set to total Positive offset for its sine wave output; PCB sample, tissue set,
parasite set, ferritin, WBCs, beta glucan.
Methods: Find several tapeworm stages at a tissue such as liver, pancreas, muscle, tumor,
using the Syncrometer®. Also search for ferritin coated WBCs, absence of beta glucans, presence of
PCBs, metals. Set the sine wave generator to the top frequency for the tapeworm found using the
table of frequencies on page 158. Attach the hot lead from the generator to a foot electrode, since
PCBs accumulate in skin, particularly in the upper body, making hand and wrist connections
ineffective. Attach the cold lead to the other foot electrode. Also attach the plate-zapper electrodes
to the feet. You will have two sets of output cables going to the foot electrodes. Do not place
tapeworm stages, flukes or fungi on the plates, only the location. And emerging pathogens.
Choose every seventh or every fifth frequency within the frequency range of the tapeworm
chosen depending on available time. You may also choose to zap one KHz at a time. Zap for five
minutes at each frequency chosen. Total voltage may range from 10 to 16 volts.
Note: Digital reading frequency generators (where you push a button to get a very precise
frequency) have not been tested yet. The constant flicker of the output in knob-controlled generators
may have an advantage over push button controlled units.
After completing the series of frequency settings, test yourself for the tapeworm you zapped at
the location selected and nearby locations. Also test for PCBs and ferritin coating of WBCs at the
organ that was zapped.
Results: All tapeworms and their stages, flukes and their stages, the bacteria and viruses not
placed on the plates as well as those placed on the plates, are now Negative at the location zapped.
Neighboring tissues are not affected. PCBs are also Negative even though they were Positive
before. A much broader killing effect is seen than was expected.
Note: How can PCBs be zapped? They are not a living entity. Has immunity been restored to
WBCs? Search at the organ-plus-WBC location for any of the items recently zapped. They will
now be present showing that immunity has been restored. Also test for beta glucans at WBCs; they
will now be present, too. Beta glucans are molecules, that are a necessary part of the WBC surface.
They use it to communicate with other WBCs. When PCBs are present, beta glucans are not. As
soon as PCBs are gone, beta glucans return. Search for PCBs in WBCs; they are present now. This
could explain their clearance from the organ zapped. Search for ferritin on WBCs; it will be gone.
But often ferritin was not there to begin with. How can the immune recovery be explained if not
through a de-ferritinizing mechanism? By eliminating lanthanides?
Conclusions: In a single sweep through the frequencies of tapeworms, all the parasites and
even mold spores can be eliminated from a site chosen to be zapped. Only emergers remain,
Bakers’ yeast, Flu virus (and sometimes its offspring, a prion), Salmonella, Pneumocystis.

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Evidently these are not killed due to their constant release from dying hosts and escape from the
tissue on the plate.

Emerging Pathogens
Bakers’ yeast, salmonella varieties, Staphylococcus aureus, Streptococcus pneumoniae, Flu
virus, Adenovirus and other small entities will emerge from killed parasites. Place these on the
other plate. This placement is to prevent survival and dispersal of entities that escape from killed
parasites. These can give you an instant cold, dizziness, fatigue, etc., unless promptly killed.

Exp. 119 Killing Emerging Pathogens

Purpose: To observe the absence of emerging pathogens after placing them, preventively, on
the zapper plate.
Materials: Plate-zapper, sine wave frequency generator set at total Positive offset, tissue set,
Flu, 3 varieties of salmonella, mycoplasma, Bakers’ yeast, adenovirus, Sorghum mold, tapeworm
eggs, Staphylococcus aureus, Streptococcus pneumoniae.
Methods: Start double-zapping at some suitably high frequency like 487 KHz, which is near
the upper limit of most tapeworm frequencies. This is an arbitrary choice. Place any of the above
pathogens and any other pathogen that is particularly troublesome on the second plate. Keep plate
additions to a minimum, however. Choose steps of 7 KHz or 5 KHz, zapping for five to seven
minutes at each frequency.
After reaching 400 KHz select any other frequency that is particularly troublesome to you
personally, for example, the Schistosoma japonicum family, which causes pain (it is always
associated with Streptococcus pneumoniae). These have frequencies 367, 366, 365, 364, KHz.
Remove schistosome entities from the plates if you plan to kill by frequency. If double-zapping at
this frequency set gives you instant relief from pain, you very likely have this blood fluke as a cause
of chronic pain.
Results: You will not get ill from zapping “too much” but from failing to kill the emerging
pathogens. By placing the offenders on the plate or zapping their frequencies immediately after the
tapeworm series, you avoid after-effects. But you should know to which pathogens you are most
susceptible. Flu and the salmonella bacteria, Bakers’ yeast and Sorghum mold are ubiquitous in us
and should always be put on the zapping plate.

Exp. 120 Zapping The Zapping Symptoms

Introduction: Theoretically, symptoms that are after effects of zapping can be avoided. By
making the zap powerful enough to kill not only the parasite designated but also the parasites,
spores, bacteria and fungal spores it carries within, they do not develop later. But, in practice, this
is not always accomplished. The reasons are:

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You may not know what pathogens will be released and therefore don’t include them on the
plate.
They flee via your blood and once away from the organ on the plate they are no longer getting
zapped.
Some emerging pathogens multiply in the brain (where you feel them) long after the parasite
itself is killed.
Fungal spores and bacteria may enter the dead parasite from neighboring regions and from
blood or lymph to culture in the refuse.
Purpose: To observe symptoms arising even from complete zapping.
Materials: The same as for previous experiment (double zapper), tapeworm set, fluke set,
bacteria and virus set, fungi.
Methods: Zap a location with the double zapper starting at 487 KHz and continuing
downward to 400 KHz. Use only preventive pathogens on the plates. When done, test yourself for
Flu, Salmonella, Bakers’ yeast, Pneumocystis, Streptococcus, and Staphylococcus at the
cerebrum.
Results: You will probably find a Salmonella or Flu virus present even though they were on
the plate while zapping. Remember they are escaping from the location on the plate to your brain
where they are not being zapped; so they can easily multiply. Salmonella’s chief symptom is
dizziness, disorientation, lack of normal anxiety (a casual attitude toward missing work), raised
body temperature (fever). The Flu’s chief symptoms are catching a cold, fatigue, and loss of
appetite, minor aches. Together, these two pathogens may send you to bed for a day with the ceiling
spinning and the bathroom too far away for comfort. To avoid this, use Lugol’s (6 drops in ½cup
water) immediately after zapping and three more times that day. To stop Flu from worsening, use 1
dose Oscillococcinum, but ONLY if flu symptoms are really present. Quassia tea can also kill Flu
virus. Drink ¼ cup, up to four times a day. Zapping Flu by frequency is even faster (324, 320, 316,
313 KHz). You may be well again before completing the set of numbers.
Comments: It is quite a bit faster to zap an acute symptom by frequency than by plate since
you don’t know which location to use on the plate. But for the frequency treatment you must know
the offending pathogen. If you can’t test, zap Flu first, followed by the three major salmonellas
together; now you have covered the most probable offenders. If symptoms are lessened or even
gone, rest and go to bed.
The third most important emerging pathogen is Pneumocystis; it too causes dizziness if in the
cerebrum. Myrrh can be taken preventively (6 to 10 drops while zapping). If there are lung
symptoms it is wise to keep Pneumocystis on the plate permanently.

Setting Up The Double Zapper

The Sine Wave Generator: Set the frequency to about 500 KHz, maximize the voltage
(amplitude) and adjust the Positive offset to a mid-scale value. Observe the output on an
oscilloscope, after setting the “ground” position at zero. Adjust the Positive offset till the entire
waveform is above the zero line or exactly on it. This may not be possible unless the amplitude is
reduced. Find the critical amplitude and offset settings and mark their locations on the generator.

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The Square Wave Generator: Set the frequency to about 30 KHz. Set voltage to maximum.
Set Positive offset to a midrange value. Observe the output on an oscilloscope. Find a combination
of amplitude and offset that allows the entire output to be totally Positive offset. Mark these
locations.
Combining the Waveforms: Combine the hot leads and the two grounds and observe the
output on the oscilloscope. Minor adjustments may still be needed to be sure the result is totally
Positive offset.

Exp. 121 PCBs Interfere With Zapper Action

Purpose: To observe interference of zapper effectiveness in the presence of PCBs.
Materials: A homemade PCB test sample, or a PCB copy in a water bottle (see Exp. 96), a
regular or plate-zapper, tissue set, toxin set.
Methods: Find a location where PCBs are present. Search the same location for tapeworm
stages, flukes, Ascaris, bacteria, viruses, fungi and toxins.
Put this location on the plate; also put the PCB sample on the plate. Zap for twenty minutes
straight. Test again for PCBs and other items. Note that they are still there. Zap again, with a
regular zapper (no plate attachment). Zap for a longer time such as an hour. Notice that this location
is still unaffected. A few exceptions do occur. Keep a list of these.
Conclusion: The zapper current does not reach PCB containing regions, even when the time
(or voltage) is increased. My interpretation is that the insulating properties of PCBs resist
penetration of the current. Yet, when the double-zapper is used, PCBs are removed effectively.
Question: Could a way of penetration be found, without resorting to double-zapping?
Note: There are bioaccumulations at PCB containing regions that are much greater than at
other locations.

Exp. 122 Zapping PCBs With Blood Vessel Access

To Organs
Purpose: To zap out PCBs with a 9 volt plate-zapper.
Materials: PCB test sample (for homemade PCB sample, see Exp. 111), plate-zapper, tissue
set, (including artery, vein, capillary, lymph vessel, lymph vessel with valve, vein with valve),
parasite and bacteria sets.
Methods: Find a location that has PCBs. Also test for malonic acid, which represents all
tapeworm stages. There will also be flukes, Ascaris, fungi, bacteria and viruses. Place this organ
on the plate. Place the artery slide on the same plate so that the two slides touch along an edge. Test
again for PCBs, malonic acid, flukes, fungi, etc. Note that together they may be Positive for PCBs
as before. Remove the artery slide and replace with a vein slide. Test again. The results may be
Positive or Negative for PCBs. If Positive, test for malonic acid, flukes, etc. Next, replace the vein
slide with a capillary slide. Repeat testing. Next, replace with a lymph vessel, lymph vessel with
valve, vein with valve. Make a list of those combinations that allow the initial Positive test result
to be heard and those that do not.

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For Example: You find the cerebrum tests Positive for PCBs and the usual bioaccumulation.
But plate-zapping will not clear any of it. By adding an artery slide in a contact arrangement, you
can easily hear the original Positive signal. Now zap again, at the cerebrum-contacting-artery
location for twenty minutes. Retest. You will now see that PCBs and all other accumulated
parasites and toxins are gone at this “extended” location as well as the cerebrum by itself.
Conclusion: You have accessed an organ that had high resistance to zapper current simply by
using its normal access routes, the arteries or veins or capillaries. However, the fact that you have
cleared the cerebral-arterial routes does not mean the lymphatic connections or nerve connections
are cleared. Repeat these tests as you did originally. They will still be Positive.
Question 1. Could you use the other access routes, in fact, all the access routes together to
clean up the location faster? Yes. You can make two or three sets of the access routes, combining
one set at a time with the cerebrum slide. Each slide of the set must touch the cerebrum slide. Q2.
Could you copy several access routes into one bottle as described in Exp. 96? Yes. Be sure to test
the bottle for the presence of each slide before labeling it.

Exp. 123 Zapping A Large Body Area For PCBs

Purpose: To observe that using arteries, veins, capillaries, nerves, ganglia connected to an
organ that has PCBs, allows it all to be cleared together in a single twenty-minute zap.
Materials: PCB sample, parasite and toxin sets, tissue sets, plate-zapper.
Part A. Methods: Place the tissue to be cleared on the plate. Arrange as many slides as you
can in a contact-relationship with the tissue, using about 1 inch of contact edge for each pair. When
you are out of room place the remainder on the neighboring plate. Zap for twenty minutes. Test each
location separately later (that is, tissue plus artery, tissue plus vein, etc.). Note that they are all
cleared EXCEPT those that were placed on the neighboring plate. They were not in contact.
Question: Will you be able to zap the leftover slides if you fuse them with the original
location? Not necessarily. You may need better access to it. To be sure you will reach it with the
zapper current, arrange the leftover slides in contact with the original location (cerebrum) and test
for PCBs again. If you cannot hear a Positive result for the new group, it, in turn, will not get
zapped. Add slides one at a time, trying different arrangements until you do get a Positive result for
the whole combination. Then zap that arrangement. It must be exactly the same when zapping. Test
again. Each component should now be Negative for PCBs.
Conclusion: You can clear a larger tissue region of PCBs and its bioaccumulations by
arranging access routes toward it for the current from the zapper to follow. The routes must be
designed to reflect the real connections in the tissue. Any design that gives you a Positive result
when tested by the Syncrometer® can also be reached by the zapper current. The vascular system
and nerves are always good candidates.
Discussion: Even when PCBs are not inhibiting current penetration it is useful to zap a much
larger region of tissue than simply using one location. And when killing parasites of the kind that
travel via the blood stream (Schistosomes) and nerves (viruses), a much greater effect can be seen
by combining these routes with a particular organ and clearing them all together.

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Part B. Combine other parts of the vascular system with the organ and test again for PCBs.
For instance, lymph, lymph vessel, lymph vessel with valve, vein with valve. Zap with this
combination next.

Exp. 124 Identifying Lymph Nodes For Zapping Or

Testing
Object: To identify a particular group of lymph nodes for the purpose of testing or zapping
them.
Introduction: In the lymphomas, lymph nodes are enlarged, often causing pressure on vital
organs nearby. Since there are numerous lymph nodes distributed throughout the body, our task is to
select the correct ones for testing and zapping. The enlarged lymph nodes can be seen bulging out at
the neck or may be seen on a scan to lie between the lungs or along the spine, or elsewhere. There
may only be a few that are involved in the cancer; yet, to zap them or explore them, we must first
find them electronically. To do this you must look for the nearest bone or other organ that you can
find electronically. Then test the combination to see if tumor-causing substances are present. If so,
it suggests that you do indeed have the right ones targeted.
Example 1: The lymph nodes at the neck.
Materials: Specimens of the two lower and two upper jawbones, lymph node slide.
Methods: Search for PCBs, malonic acid, DNA, clostridium bacteria, asbestos, azo dyes,
copper, cobalt, vanadium and the other usual tumor toxins in the lymph nodes by simply placing
your lymph node slide on the plate. If you get a Positive result, the current is already reaching one
or more of the tumor-involved ones; you would of course immediately clean this up by plate-
zapping this lymph node slide plus access routes (arteries, veins, capillaries, lymph vessels, etc.).
Plate-zapping this way will clean up enough of them so that the Syncrometer® can no longer
detect any more using this lymph node slide. To find the remaining ones you must pinpoint them
more accurately.
Place the lower jawbone that is on the side of the enlarged lymph nodes (right or left) on the
test plate. (A copied bottle will do). Place the lymph node slide beside the jawbone, touching it so
that no portion of the bone overhangs the slide. The part of the bone that touches the slide must also
be very close to the plate, not a few mm higher. The contact must be as near the plate as possible, to
be within the electric field of the (capacitor) plate.
First, ascertain that the jawbone itself does not contain the set of tumor related entities by
testing it. Then retest with the lymph node touching the bone. You may now get Positive results for
the tumor toxins, while the lymph node alone or jawbone alone was Negative. You can now treat
this duo as if it were a single organ. Search for immune problems first so they can be corrected
first. If PCBs are present, you will need artery, vein, capillary and the remaining connections to this
same lymph node. To achieve this, place each new slide so it touches the other slides on the plate,
but keeping the original bone-slide connection intact.
Note the following dilemma: Since the bone-lymph node combination already tests Positive,
a new slide placed touching it cannot logically be tested. If it is Negative, the overall combination
of three will still be Positive; if it is Positive, it cannot be distinguished from the results for the
duo. If you could first zap the duo so it is Negative for all toxins, then the next slide placed in

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attachment would give a clear result, whether Positive or Negative. But one cannot reach the duo
with a powerful zap that clears all toxins unless access is created for the current along blood
vessels and nerves.
In view of this dilemma, you can use a “shotgun” approach. First add the arteries, veins,
capillaries as a group (group A, standing for arteries and nerves), and zap. Then exchange these for
lymph vessels, lymph, lymph valves, vein vessels, vein valves as a group (group L, for lymphatics).
After these two zaps, the lymph node-bone duo will be Negative. Now you can test any other tissue
nearby, such as cartilage, connective tissue, and others.
Example 2: Lymph nodes near the spine can be identified by choosing a number of vertebrae
that are possible neighbors. Place a vertebra and the lymph node slide touching each other with the
same restrictions as before. Then add access routes, test and zap.
Example 3: Lymph nodes near the tongue, trachea, esophagus, lungs can be found by placing
the access routes between the organ and lymph node. Lymph nodes in the space between the lungs,
called the mediastinum are particularly hazardous and difficult to reach surgically. By using heart
or lung or esophagus as a marker organ, you may be able to zap these repeatedly till they shrink.
Your arrangements might be right lung-group A-lymph node, in one zap followed by right lung-
group L-lymph node in a second zap.
Example 4: Lymph nodes associated with various portions of the intestinal tract can be found
by placing the access routes between the lymph node and intestinal slide. Since these portions are
quite long, this still leaves a measure of precision to be desired.
Example 5: Lymph nodes in the groin area are often painful or enlarged for various reasons.
These may be reachable beginning with a sacral spinal cord slide contacting the sacrum (bone),
which, in turn, is contacted by an access route, and finally by a lymph node slide.
Conclusion: The rule for discovering the electronic location of an organ is to find its true
physical connection to another organ. This is best exemplified by noting that you can zap two
adjacent vertebrae by touching them together on the plate, but you cannot zap any other two in a
single zap.

Exp. 125 Finding Organs Using A Coin On Your

Skin
Purpose: To find a special lymph node or organ like retina, optic nerve, adrenal gland
directly, using a coin.
Materials: Two identical quarters or dimes (for small regions), a paper dowel standoff to
hold the coin tightly against skin, several slides of organ sought.
To make a paper dowel standoff fold a double paper towel in half lengthwise, twice. Then
roll tightly and tape with clear tape.
Methods: Place one coin on the plate of a Syncrometer®. Hold its mate over the lymph node
to be electronically “found” somewhere below the skin areas, using the paper dowel. Place one
lymph node slide on the other plate; search for resonance. You can now test or monitor this lymph
node or organ. (To zap this organ see Exp. 128, skin-zapping). Replace the lymph node slide with
entities to search for. Then move the coin around, searching for a spot that lets you hear

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resonance with another lymph node slide on the plate. If searching for two minutes does not yield a
Positive result, try yet another lymph node slide.

Exp. 126 Finding Right And Left Organs

Discussion: It is important to have the correct organ sample on the plate, as close a match as
possible with the site you are investigating or zapping. The right and left organs of a pair do not
resonate, whereas two rights or two lefts do.
Purpose: To find right and left organ slides or specimens; to identify your slides.
Materials: Several slides of the same organ.
Methods: Select those organs for which you have a right and left one. For example kidney,
lung, adrenal, leg bones, arm bones, eyes, thyroid, thymus, liver (this also has a middle region).
Place a coin (quarter or dime preferred) on the skin over the spot you believe is on top of the
organ, for example kidney. Place an identical coin on the Syncrometer® plate. Place one of your
kidney slides or specimens on the other plate. Press the coin on the skin with a paper dowel (with
at least an inch of standoff distance), while testing for resonance. If there is no resonance, move the
skin coin to new locations in the same vicinity in an effort to find the organ (kidney). If you find a
location that resonates, you have found this organ on the current path traced out by the
Syncrometer®. Label the slide right, left, or middle. Repeat for all your slides.
Note: Remember that a part of the body’s metabolism is turned ON or OFF at the exact time
:00. It is easy to find the OFF minutes; they occur at odd minutes. Always test for two minutes to be
very certain of your matching accuracy.
Also, remember that azo dyes flip this timing so that ON occurs in odd minutes. Search for
dyes in such an organ.
Definition of an odd minute: on a digital clock the number appearing is odd. In other words,
the time is going into an even minute (This is my definition, not an official one).

Exp. 127 Finding An Unidentifiable Tumor

Discussion: Small round nodules visible on scans or X-rays are usually enlarged, very dense
lymph nodes. But when they occur along scars from previous surgery, they may have no
identification. Even though the original cancer stemmed from the lung or stomach the new tumors
may not. Yet you need to find them electrically to be able to test and zap them. Many other kinds of
tumors are also without identification; yet need to be “found”.
Purpose: To find tumors for zapping.
Materials: Two cat skeletons, one assembled, and one taken apart (see Supplies Used For
Testing page 161), anatomy set of slides, toxin kit.
Methods: If you can actually feel the tumor or lump you may get an idea where it is in
relation to the nearest organs. If you must rely on scans, notice which organs are nearest to it. Put
the nearest organ on the Syncrometer® plate. Test this organ first to see if it, too, has the tumor
related substances: dyes, asbestos, dental plastic, Clostridium, DNA, etc. If it does, it should be
cleared first of these. Attach the access groups A and L, in turn, for two plate-zaps. Now the

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neighboring organ tests Negative for tumor content, so we may use it to find a pathway to the
unidentified tumor. Attach a tricalcium phosphate specimen (representing tumor) to the duo; now
you have the neighboring organ, touching the arteries of group A, which is further touched by
tricalciumphosphate (a trio). Test for tumor contents. If they are Positive, you have found the tumor.
If they are Negative, repeat the test using the lymphatic group (L) in the middle of the series instead
of the arterial group. If no tumor contents can be found, you are not at a tumor. Select a different
neighboring organ.
Note: From a practical standpoint, you can of course zap these neighboring organs anyway,
since this is returning more and more immune power to you. But the principle that is made clear in
this experiment is that you can mimic the actual connections of tissues with electrical connections
and find that you can locate otherwise unidentifiable regions for study or for zapping.
Example: A tumor in the abdominal cavity is very painful, requiring morphine. It is not
known whether it is attached to a piece of bowel, the kidney, the bladder, the uterus, and the
muscles because the scan does not make this clear.
Since the pain would travel up the spine, we can assume a connection to the spinal cord.
Arrange sacral spinal cord slide, touched by sacrum (lowest cat vertebra), touched by skeletal
muscle, touched by group A access specimen, touched by tricalcium phosphate (5 items in a row).
If this does not test Positive for dyes, asbestos, thulium (lanthanide representative), Clostridium,
malonate, etc. you have not reached the tumor. Move higher up the spine. Counting from the bottom
of the cat skeleton spine, choose the second vertebra, not the first (from the tail end). Attach it to the
sacral spinal cord slide without any overhang. Add skeletal muscle, etc. and test again. Continue
testing higher vertebrae; also test the lumbar section of spinal cord. When you find resonance, you
are at the tumor. You can now search and zap on target. Several zaps here, followed by zapping
added tissues, such as adipose, connective, mucous, mesothelium, in turn will relieve pain and
begin to clear away the tumor.
Skin-Zapping
The skin with its layer of fat (adipose) tissue just beneath it becomes a huge storage tank for
toxic solvents that cannot be metabolized easily by the body. Chief among these are PCBs, freon
and benzene. Deep under the skin, in their favorite location, the lymph valves are innumerable
Fasciola adults along with Schistosomes, Dipetalonema and other parasites, eggs and stages of all
kinds. Recall that killing Fasciola with herbs or weak zaps leads immediately to Sorghum mold
growth. When this is killed, the metal cobalt is produced and new fungi grow. In an advanced
cancer patient you will find numerous parasites, numerous fungi and all the tumor-related metals in
the skin, showing a long history of parasitism for the patient. It would be impossible to kill all these
using internal access routes for the current. With our limited ability to specifically zap a certain
location, clearing the body’s lymphatic valves would require an infinite number of zaps. But a 3 ½”
square of metal, such as is used for the zapper plates can achieve an initial complete skin-zapping
in seven to ten days.

Exp. 128 Zapping Parasites Through The Skin

Part A. Purpose: To clear the skin, with its attached underlying tissues, of PCBs, parasites,
and particularly Fasciola and Clonorchis (human liver fluke) adults and eggs. This will remove a

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significant growth factor, Transforming Growth Factor (TGF), which is produced by Clonorchis.
An oncovirus bearing the oncogene cFos is produced by Fasciola along with Fibroblast Growth
Factor (FGF) and fibronectin (FN). These growth factors spread widely through the body until the
parasites are killed. Then they stop abruptly.
Materials: An extra 3 ½” zapping plate or equivalent sheet of metal with corners and edges
filed smooth to make them safe; plate-zapper, an extra banana-to-alligator clip lead, lymph valve
slide, parasite kit.
Methods: Press a quarter (coin) against the skin using a paper dowel to avoid touching it
with fingers. Press hard. Place an identical quarter on the Syncrometer® plate. Search for a lymph
vessel valve in the current path by placing it on the other plate and hearing resonance. There will
almost always be one. Next place the lymph valve slide beside the coin on the plate and touching it.
Now search for entities at the valve by placing them on the other plate, such as PCBs, freon,
tapeworm larval stages and eggs, malonic acid, flukes and their stages, Ascaris, bacteria, fungi and
yeasts, viruses, besides Fasciola and Clonorchis adults.
You could, of course, zap along a current path to your coin simply by taping it down tightly.
But a larger area can be cleared by using the 3 1/2” square as one of the electrodes. Tie a cloth
scarf tightly around your body, insert the square plate with the smooth side against the skin and
attach the hot lead coming from the zapper-plate. Use an empty vitamin bottle under the “belt” to
press down as hard as possible on the plate while zapping. Alternatively you may press on it by
hand, using a paper dowel. An elastic belt, such as carpenters’ back support, with its Velcro ends
can be cut down the middle, making two. The metal square should be attached with screw and nut
piercing the belt for ease in adjusting it.
Connect the “ground” side of the zapper to a foot or hand electrode. PCB-loaded persons
should use feet on the electrode. The heel is least likely to be saturated. Arrange the plates with the
following: lymph vessel, lymph vessel valve, vein, and vein valve (or group L) on one plate.
Emergers are placed on the other plate: cFos, Sorghum mold, Bakers’ yeast, Flu, Salmonella,
Hepatitis B, Clostridium botulinum. An advanced cancer patient should place 3 clostridium
bacteria on the protective plate. Zap twenty minutes. Next zap with only group A on the location
plate. Then move the square to the next spot after outlining around it with a pen to keep track of the
area covered. For curved locations, use a plate that has been cut in half or quarters. File the edges
very smooth to avoid losing most of the current here and even producing minor “burns”. Keep
constant vigilance over this plate, moving it or wetting it when itching occurs. Cleaning the skin
with ethyl alcohol helps prevent burns.
Retest for PCBs, Fasciola, Fasciola eggs, cFos, Sorghum mold, and cobalt. It should all be
gone. Evidently the body can completely clear one current path at a time when done this way. The
skin plate itself specifies a location and the vascular groups on the zapper plate create the access.
Test the skin again soon for Fasciola at lymph valves. There will still be a number of them
that were missed. There will also be Fasciola metacercaria at the capillaries unless group A has
been zapped. You may repeat skin-zapping or use the large dose of Green Black Walnut daily to
speed up the whole program of deparasitizing.
Comments: Be sure to take or recommend a large dose of digestive enzymes to remove the
newly killed parasites. Do this within an hour of completion of zapping, to avoid mold invasion and
cobalt release later.
Part B. In cancer that has progressed to a malignancy, Fasciolopsis buskii occupies the
lymph valves. Fasciola stays about 2 inches away in a wide circle. Many Fasciolopsis buskii can

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be found in the skin over the tumor region. They often form a line, as though in single file, along the
fallopian tubes or transverse colon or the pancreas. Search your body in these locations.

Exp. 129 Finding a Skin Lesion

Part 1. Purpose: To test or zap a blemish on skin.
Materials: Ink pen, dime.
Methods: Using an ink pen, fill in a small area on top of a wart or skin blemish. For moles or
open lesions apply a piece of clear tape first; then color in a small spot on top of the tape. Next
make a larger spot (about ½-inch square) on a piece of white paper towel using the same pen. Place
this piece of paper in a plastic cup; cover with water (about 1/8”). This ink patch is your test
substance. The ink patch on your skin is the location that will resonate the circuit. Now search for
as many items as are of interest at that location. You may find RAS, JUN, Sorghum mold, and
numerous other items in the blemish. A brown spot usually has Aspergillus and Penicillium fungi
and copper. The copper probably is used by the body to make melanin, brown pigment. A mole
usually has live Paragonimus in addition to fungus, copper, and other items.
To zap this spot, place a dime over it, taping it down tightly and connecting it by alligator
clip to the zapper plate. Place the arterial group on the plate for one zap and the lymphatic group for
a second zap. Put Flu and Salmonella on the emergers’ plate.
Comments: You may see a quick reduction in size of the lesion in the next few days. It may
grow again after that. A fresh analysis may show new yeast or fungus or virus is present. Zap
repeatedly. Try to find the source of the invaders.
Deeper under the skin below the blemish you can find lymph valves, lymph vessels and
capillaries that are invaded by parasites and fungi, most commonly Fasciola. The growth factors
and viruses coming from these seep upward toward the skin, probably preventing its healing.
Part 2. Mark a spot with a different color ink pen, right beside the original ink mark (not
more than 1/16” away), and test for the same items found originally. You cannot find them because
there is no resonance to this new spot.

Exp. 130 Killing Fasciola In Skin With Herbs

Purpose: Part 1. To kill all Fasciola parasites and stages in the lymph valves under the skin.
Materials and Methods: 10 tsp. Green Black Walnut Hull tincture, extra strength, from a
freshly opened bottle. Combine with whipping cream, maple syrup or honey, and 10 drops of
peppermint oil. Sip all in 1/2 hour. Stay seated. If nausea strikes, eat bits of bread. Go to bed.
Results: All Fasciola and stages should be gone. Repeat in three days to catch any
stragglers. Repeat daily if very ill with Cancer.
Part 2. To kill all Fasciola metacercaria in the capillaries under the skin.
Materials: 9 capsules wormwood in a single dose.
Comments: It is obviously beneficial to take the wormwood dose just before or after the
Black Walnut, and to be zapping at the same time. Try to arrange this.

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Part 3. Use 20 capsules freeze-dried Black Walnut instead of 10 tsp. tincture. But in severe
illness use 30. Take with peppermint spiced beverage to prevent nausea.

Exp. 131 Zapping Out Pain

Discussion: Since all pain locations studied so far show the presence of Streptococcus
pneumoniae, I consider this bacterium to be the most important pain causer. Since any larger
parasite that characteristically brings with it Strep pneumoniae, would appear to be the pain
causer, it is important to distinguish the two.
Preliminary Observations: So far, two parasites have been found to bring with them Strep
pneumoniae: the Rabbit Fluke, Hasstilesia, and a blood fluke, Schistosoma japonicum. When Strep
pneu arrives with the Rabbit Fluke, it does not cause a pain attack; it merely distributes itself to
various locations. But when it arrives with Schistosoma japonicum, it produces pain readily and
acutely.
In two diseases involving pain, chronic arthritis and cancer, both Schistosoma japonicum
and Strep pneumoniae have invaded the body in many places and are thoroughly entrenched.
Capillaries, veins and vein valves seem to be the favorite locations for Schistosoma
japonicum. Simply killing them there helps reduce pain. But, of course, this is temporary, since
new populations arrive via the blood.
Many persons harbor Schistosoma japonicum without pain. In them, the associated
Streptococcus pneumoniae are at various locations and in low numbers.
Many persons harbor other varieties of Schistosomes and pain is not part of their effects.
At locations of pain, phenol is found. It cannot yet be ascertained whether phenol is produced
before or after Strep pneu appears. By combining phenol with magnesium (oxide), about 600 mg, it
can be removed temporarily, and pain is reduced during this time. The true sources of phenol are
not yet clear (see Exp. 54 to 57).
In view of the complex nature of pain it seems wise to at least kill the Schistosome invaders
and Streptococcus pneu. constantly.
Purpose: To eliminate pain temporarily in a few zaps.
Materials: Tissue slides of organs involved in pain, spinal cord slides, vertebrae for the
spine section involved, the arterial group (A), the lymphatic group (L), Schistosoma japonicum
female and egg slides, Streptococcus pneumoniae, bladder, scar tissue.
Methods: Search for Schistosoma japonicum eggs or females at many locations in the body
including the site of pain. Similarly search for Strep. pneumoniae and phenol. They will all occur
together in most places. Arrange for plate-zapping: place the main organ involved in pain on the
plate, attach group A and verify that the pain makers are there by finding resonance. Attach the
vertebrae or a single vertebra near this organ, as well as a section of spinal cord at this level.
Verify that the pain makers are still reachable. Zap for twenty minutes. Next, exchange group A for
group L and repeat the zap for twenty minutes. Relief should be felt after the first or second zap.
However, if time allows, neighboring organs should be similarly cleared, as should the
bladder.
The plate for emergers should have Schistosoma japonicum eggs and females, Streptococcus
pneumoniae, Flu, salmonella varieties, Baker’s yeast and Sorghum mold.

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Conclusion: Much more research is needed to be able to quickly and reliably resolve any
pain problem. Daily zapping the pain areas does reduce the severity and frequency of its return. So
zapping for pain daily and in places where there is no pain is a useful procedure. It is, of course,
not necessary to test first in order to zap. But keeping notes on results of testing or zapping is
valuable for future reference.

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Cancer

Exp. 132 How To Find and Destroy An Advanced

Cancer In 8 Steps (Days)
Purpose: To turn around an advanced cancer patient in about one week with a Mostly
Zapping program. This means changing a terminal picture to one of hope, but with a sense of
security, meaning the patient says they feel much better, can eat, can perform their usual functions
and plainly volunteers that a corner of some kind has been turned, for the better, and without drugs.
Getting fully well, shrinking the tumors substantially, and lowering clinical cancer markers
significantly is NOT included in this time frame. These goals must be pursued with the 21-DAY
PROGRAM discussed in the book Cure For All Advanced Cancers. By combining the Mostly
Zapping program with the 21-DAY PROGRAM and intravenous therapy when needed, virtually
every cancer patient can be saved, even if organ failure has already begun.
Note: Of course, it is not necessary to do Syncrometer® testing while treating the patient. But
testing adds the scientific element and creates a research base besides giving individuality to the
patient. Do as much testing as possible using previous experiments to guide you.

Rules for Self Health Therapists

I believe these rules are somewhat more stringent than the
Hippocratic oath, which clinical doctors take. In the rule to “Do No Harm”
the concept is a slippery one that anyone could bend to his or her own
purposes. After all, one must always weigh harm against benefit and this is
done subjectively.
My proposed first Self Health rule is: Give nothing to the patient or
anyone seeking your advice that you have not taken yourself. If you have
taken this Self Health Oath, the patient can feel assured that they are in safe
and honest hands. You may not wish to take Lugol’s iodine drops and don’t
need to, but you will go through the minor misery that makes you honest
when you say “It’s not too unpleasant, even for a child, but holding your
breath while drinking helps.”
This first Self Health Oath is not meant to be a vague generalization
like the Hippocratic Oath. It is meant literally. On every description pad
listing supplements and procedures a column is devoted to check marks if
the therapist has ever done it herself or himself. This does not mean
identical amounts have been taken for identical times, only that the item has
been tried.

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Materials needed by the therapist and patient: Test substances, pathogen kits in slide or
bottle-copied form, supplement schedule, and zapping schedule, all listed on pages 137, 136, 128
and 131. Sources for items listed are given in Supplies Used for Testing chapter.
Part I (Visit 1)
Test for OPTyr at “whole body”, namely without a tissue specimen on the other plate.
Whether the result is Positive or Negative, test next at the organ thought to be involved. Very rarely,
about 1% of cases, OPTyr will be Positive at an organ but Negative at whole body testing. As a
final check, if OPTyr is still Negative, search through the skin with a coin, as close as possible to
the suspected location of the cancer. Mark this spot with an ink pen if Positive. These extra tests
assure you that a very early malignancy is not being missed.
If OPTyr is Positive, immediately test a dozen other organs where malignancy may be
spreading unbeknown to your patient or the oncologist. Search at least in colon, bone, lungs, breast,
prostate, lymph node, liver, pancreas, and brain.
Search at the “whole body” for copper, cobalt, mercury, lead, vanadium, urethane, bisphenol,
malonic acid, DAB dye, Sudan Black B dye, Fast Green dye, Fast Garnet dye, Fast Red Violet dye,
germanium, chromium, nickel, asbestos. Also, Baker’s yeast, Fission yeast, PCBs, freon,
Salmonella, benzene, thulium. This lets you know which items are overwhelming his/her body. It
also lets the patient know what the highest priority items are that must be removed from his/her
home and environment.
Note: If this panoramic toxin test is delayed to later visits, some will be gone due to leaving
home. You may retrieve some of this information by testing dust and water samples from home at
anytime later in the schedule.
Order the appropriate scan (ultrasound, CT, or MRI, without contrast material being injected
since these contain lanthanides that do not leave the body). This will give you and the patient the
beginning picture.
Start plate-zapping. Place the following slides or bottles on the left plate. Slashes indicate
that they touch each other. The first four zaps should be in this order if possible:
1. blood/WBC
2. artery/vein/capillary (or group A)
3. lymph/lymph vessel/lymph valve/vein valve (or group L)
4. the tumorous organ such as liver, lung, etc., combined with A; and secondly combined with
L. The sixth zap will be right on the tumor. First we must specify the tumor by adding tricalcium
phosphate to the tumorous organ.
Place the specimen of tumorous organ plus tricalcium phosphate plus arterial group (A)
together on the plate so that they touch each other. They may be arranged in triangular fashion or in
a line, but the arterial group must be touching the organ, not merely the tricalcium phosphate.
Next zap the tumor with the lymphatic circulation attached, including lymph, lymph vessel,
lymph valve, vein valve (group L), all clustered together, touching each other.
On the other plate, during each zap, place the specimens of bacteria and viruses that emerge
from dead parasites. Choose mycoplasma, Flu, three salmonella varieties, Bakers’ yeast, Sorghum
mold, RAS, JUN. These should not touch each other since they are separate in real life.
Some time during zapping give the patient 2 tsp. green black walnut hull tincture, extra
strength, (up to 10 tsp. if critically ill) or 20 freeze-dried capsules and 9 wormwood. Also give 6
drops Lugol's in ½glass water plus 15 digestive enzyme capsules near the end of the session. These
will begin to digest the dead parasites and debris around the necrotic tumor and in the

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lymphatic system. Give 2 levamisole (Decaris). Give 20 drops straight oregano oil in capsule with
food (not beverage). If almost nothing can be taken by mouth, select Lugol’s, digestive enzymes,
Decaris and oregano oil. Help the caregiver find the best beverages to accompany these
supplements so a strong positive attitude develops.
Provide the caregiver with the Supplement Schedule and Zapping Schedule so he/she can
procure all items that are needed for the next day. Provide a list of next highest priority zaps to be
done at home. These are right kidney/A, right kidney/L, left kidney/A, left kidney/L.
Schedule a very complete blood test, including serum iron but omitting thyroid panel and
cholesterol panel to control cost. Include chemical cancer marker if known.
You have accomplished several things at this first visit:
1. found a growing tumor and its location
2. found the toxins responsible that the patient must clear from his/her home and body
3. cleaned the blood and lymph of parasite eggs and larvae, yeast, fungus spores, PCB,
mycoplasma and oncoviruses to stop their spread
4. started zapping the tumor to regain immunity there, so you can have the help of the white
blood cells to remove it instead of having to detoxify all its contents
5. protected the patient from “Flu and salmonella” symptoms by keeping these on the
neighboring plate during each zap (not if they are being killed by frequency)
6. started the patient on the Supplement Schedule

Part II (Visit II)

Check for OPTyr first, at all the organs that were Positive the day before. It should now be
Negative everywhere. But a search through the skin using a coin may reveal leftover spots.
If OPTyr is still Positive at some locations, search for Fasciolopsis there and isopropyl
alcohol. Plate-zap that location (skin plate-zap) after placing skin/tricalcium phosphate/A on the
plate. This zap is then repeated using the lymphatic group.
Repeat these zaps at any location still Positive for OPTyr. This will eliminate it all.
It will take much longer to eliminate excess DNA since we must eliminate clostridium
bacteria first.
Test for clostridium at tooth, colon, the tumorous organs and inside the tumors. Check the
dental panoramic X-ray and mark all teeth with plastic and metal fillings for extraction. Small
fillings and cosmetic plastic can be removed after extraction sites have healed. Make dental
appointment and at the same time the denture impression appointment.
If the patient is too ill to sit in a dental chair, teach the caregiver to floss the patient’s teeth
and brush with oregano tooth powder. (The caregiver does this to be sure it is thorough).
Review the blood test results with patient. Remind patient and caregiver to study the chapter
on reading blood tests in the book, Cure for All Advanced Cancers. Note if the RBC and platelet
count is adequate to do dental work. If not, schedule a transfusion or wait till crisis is over, giving
suitable shots, supplements and Ws. If the crisis cannot be resolved quickly, postpone dental work
but emphasize oregano oil tooth brushing.
Find the critical items on the blood test. It may be the kidneys (high BUN, creatinine), liver
(high SGOT, SGPT, GGT, bilirubin), thyroid and parathyroid (high or low calcium), clostridium
systemic invasion (low uric acid), systemic Bakers’ yeast invasion (low blood sugar), a flood of

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azo dyes (high LDH and alk phos, low BUN and creatinine, bone marrow failure), or low serum
iron (less than 35). If blood sugar, triglycerides or cholesterol are too high, be grateful.
The crisis must be dealt with first, before going on with the regular program.
For a kidney crisis, provide the kidney herb program, being sure to sonicate everything,
particularly the parsley. Teach the patient to measure the 24-hour output of urine and how to
produce a gallon of urine a day (by drinking teas and water). Give IVs if available to add to urine
volume. Give spironolactone, 100 mg, two times a day if edema already exists. Give potassium
gluconate (1 tsp. three times a day in food) to assist osmotic regulation. Give LasixTM additionally
for serious edema.
At the same time arrange for more kidney zapping, as well as adrenals and bladder.
Search at the kidney first to find the main problems. Then search for loss of immunity there
and its causes. There are only four. If the patient is bedridden, use a saliva sample. After adding a
tsp. of water, fold the plastic bag to keep specimen next to plate but also to take little plate space.
Place it beside the kidney specimen and WBCs to search for immune problems. You would now
have three things on the plate: saliva, kidney, WBC.
Regardless of which kind of crisis the patient has, or if she has none, search for immune
problems at the second visit. An organ with a crisis is also called “organ in distress”.
Place the organ in crisis or the tumor on the Syncrometer® plate (tumorous organ plus
tricalcium phosphate). Place the WBC slide nearby but not touching. Search for the toxins and
bacteria you already found in the organ itself they should all be there if the WBCs are
phagocytizing. If they are not, search for ferritin. Search for betaglucan. Search for lanthanides in
the organ itself (not the WBCs). Search for benzene and PCBs.
Try to correct the immune problem in 24-hours by removing all four at once instead of singly.
1. Start the patient on levamisole, 100 mg three times a day before meals to remove ferritin.
Sonicate all produce after hot washing. Sonicate all foods eaten except water to eliminate asbestos
from food.
2. If benzene is found, search for zearalenone. If this mycotoxin is found, search for Potato
Ring Rot fungus. Zapping will kill it. The vitamin B2 and magnesium supplement before meals will
detoxify the benzene soon but also administer an office dose yourself to get him/her started.
3. If lanthanides are found (mainly thulium, holmium and gadolinium), apply four tiny magnets
to the skin over the tumor about 3 inches apart from each other. Teach the caregiver to keep
patient’s skin hair shaved and to oversee the placement of magnets even if patient applies it
himself. Use clear tape or masking tape, not pharmacy-variety due to mercury and thallium in
medical tape. Review dental needs and food preparation (hot washes), to avoid lanthanides.
4. If betaglucan is missing in the WBCs you can expect PCBs. Although benzene could be
dispatched in a day, PCBs take much longer. Search for PCBs in skin layers with topical skin
testing. Place a quarter (coin) at nape of neck, holding it there tightly with a paper dowel about 2”
long so the assistant does not touch the patient during testing. Place a similar quarter on
Syncrometer® plate. Search for PCBs, benzene, freon and other solvents. Place the quarter at six or
seven places: along spine, at both wrists, palms of hands, soles of feet, face, chest, back. Instruct
the patient to apply the zapper electrodes where PCBs are absent since conductance is lacking
where PCBs are present. Start patient on 2 tbs. ozonated olive oil daily. This can be stored in
freezer in portions of 2 tbs. if made in advance. On subsequent days, test a urine specimen for

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PCBs to see if they are being expelled. Ozonated oil, together with intensive plate-zapping will
clear the organs.
5. Zap the organ in crisis, first with artery/vein/capillary (A) attachment, then with the
lymphatic/vein group (L), twenty minutes each.
For a kidney crisis, zap the adrenal and bladder also, two zaps each as before. Keep the same
items on the other plate.
6. Zap the tumor again, this time attaching adipose tissue and group A, followed by L (for
example, right breast/tricalcium phosphate/adipose/A).
7. Begin zapping the digestive tract, everything from the salivary glands to the recto-anal
junction. Arrange with the caregiver to procure a complete set of digestive tract-related organs or
copies of them. Give each location two zaps, one with A, one with L attached, keeping notes of
those completed. Zap only two or three digestive locations a day. Expect to see diarrhea. Instruct
the patient to delay toilet flushing in order to observe parasites. They cannot be seen in a formed
stool. Show the patient samples of different parasites; those colored pink like grapefruit are
Fasciola; those colored tan or gray, also ranging in size from ¼ inch to 1 inch, are Fasciolopsis.
Those with three obvious small red dots, 1/8” to 3/16” long are Paragonimus. All have black
“threads” (egg strings) hanging loosely from them. If the patient suspects a parasite in their stool,
request that a specimen be brought in for your examination. It must be prepared in a special way.
No other way is acceptable. After the toilet contents have settled, a plastic spoon or fork is used to
dip up the specimen into a plastic cup. Use tap water with very gentle agitation until the parasites
are “cleaned up”, then transfer to a zippered plastic bag. Add a tsp. of tap water. Now add Lugol’s
iodine, about 10 drops. The specimen bag is dipped into Lugol’s water to sterilize the outside too.
Add 6 drops Lugol’s to a plastic cup of water held over the toilet. Dip in the specimen bag. Do not
rinse. Place specimen bag in another zippered plastic bag. Then place it all into a third zippered
plastic bag for transportation to your office. This Lugol’s bottle is hereafter consigned to the
bathroom. Wash hands by dipping in Lugol’s water (1 drop per cup) or spraying with straight ethyl
alcohol.
When it arrives as instructed, remove the inner bag with gloved hands. Dip bag into Lugol’s
water and dry. If the identity is obvious you may put it under the binoculars for others to see. If it is
not obvious, search through your parasite kit for an electronic match. That will be the tentative
identity. Keep notes.
Unless the patient sees dozens and more arriving in the commode, she is not deparasitizing. If
none appear after three days of zapping digestive organs, the patient should take 1 tbs. Epsom salts
in the morning before breakfast the next day to induce a diarrhea. Or do a liver cleanse using ½cup
ozonated oil in the usual way.
The patient can be expected to complete any scheduled zaps at home. About eight hours of
zapping (24 zaps) can be expected in a day that is not filled with appointments.
Make sure the patient has four rechargeable batteries and a battery charger. Also a voltmeter
to test batteries; voltage should not begin below 9.4v. Teach caregiver how to use this equipment.
Any herbs are to be taken during the daily zaps to ensure that all eggs released by parasites
are promptly killed, not allowed to disperse. Digestive enzymes, Lugol’s, hydrangea powder and
selenite are taken throughout the zapping day to keep on digesting dead matter, so fungus cannot get
started.
You have accomplished several more things on the second day including:
1. Verified that the malignancy is gone

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2. Scheduled the dental extractions and scans

3. Reviewed the blood test and started critical care measures
4. Zapped the organ in crisis to avert failure and the tumor itself
5. Found the immune problems in both the organ in crisis and the tumor
6. Begun to repair the immune deficiency
7. Started zapping the digestive tract

Part III (Visit 3)

At some point the dental extractions are completed. On the day of extraction the patient is
instructed to stay home afterwards to do Dental Aftercare. You must check whether it is being done
correctly and a liquid diet obtained and strained. Most supplements can still be taken, if in capsule
form. Others, like powdered hydrangea can be put into capsules. Heart patients may be put on
additional antibiotics.
The patient can be asked to zap while staying home; zaps are at the critical organs, the tumor
and several digestive locations. Zaps at the critical organ and tumor should now add mucous tissue
instead of adipose and add A or L by turns. Continue zapping digestive organs. Rest is best on this
day. Only water, strained teas, juices and broths are allowed for two days after the dental surgery.
Most important supplements are digestive enzymes, Lugol’s, levamisole, selenite, and hydrangea.
The tumor scan can be studied.
If an emergency threatens or could threaten, a saliva sample brought to the office could be
searched for Salmonella, Flu, Mycoplasma, Shigella, Staphylococcus, Streptococcus,
Clostridium, Baker’s Yeast, Pneumocystis, E. coli, Coxsackie B virus, Hepatitis B virus or other
delirium producing pathogens. As soon as the Positives are found, these pathogens should be
zapped in the blood. A blood specimen is placed on one plate and the Positive pathogens all
together on the other plate. Antidotes by mouth are as follows:
Salmonella: Lugol’s iodine, 6 drops in ½cup water up to six times daily
Flu: Quassia, ¼ cup, four times a day; also Oscillococcinum homeopathic, every six hours for
two days maximum
Mycoplasma: Methylene Blue dye, 25 to 50 mg, three times a day, in capsules. Expect blue
urine
Shigella and E. coli: Turmeric and fennel, each 6 capsules three times daily
Staph and Strep: Chamomile oil, 10 drops three times daily
Clostridium: Oregano oil, 20 drops placed in a capsule three times daily with food
Bakers’ yeast: Hydrazine sulfate, a pinch or 1/16 tsp. three times daily
Pneumocystis: Myrrh, 10 drops three times daily
In spite of their superiority over antibiotics, nothing is as effective as zapping these
continually, all day, while on the second plate. Or adding their frequencies to the plate-zap for ten
minutes per frequency.
On the third day you have:
1. supervised dental work
2. continued the zapping schedule by adding a set of four tissues to the organ being zapped.

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