Bioelectronics

The next-most useful device to have is a Syncrometer.TM It lets you diagnose yourself and monitor your progress until you are cured. It consists of an audio oscillator circuit with your body as part of the circuit. Utilizing samples of parasites or pollutants, it lets you test for them in any product or body tissue. I include a design that you can make yourself.

A third very useful device is a frequency generator. You can use it to electrocute individual organisms, or together with the Syncrometer TM to find an organism's particular frequency. You need one that operates in the parasite, bacteria and virus ranges, from 50 KHz to 900 KHz. It must also be able to select a particular frequency, like 434 KHz, quickly and accurately. Frequency generators are available for as little as $300.00, but it is worth paying a little more to get a digital display of the frequency.

The Discovery

What makes me think I can find things in the human body that a blood test can not? What new technology makes this possible? Why is electronic testing superior in many ways to chemical methods? What are my claims of electrically killing parasites based on?

The method rests on radio electronic principles.,

If you match, very precisely, the capacitance and inductance properties of an external circuit so that its resonant frequency is the same as the emitted frequency coming from somewhere else, the circuit will oscillate. This means there will be positive feedback in an amplifier circuit. You can hear it. Like when a public address system squeals.

The external circuit I use is called an audio oscillator, quite easy to build or buy. Your body provides the emitted frequencies. When you combine the audio oscillator circuit with your body, and you hear resonance, then you have detected a match! Something in your body matches something in the circuit on the test plate. By putting a laboratory sample of, say, a virus on the test plate, you can determine if your body has that virus by listening for resonance. Hearing resonance is easy if you're a radio technician or musician. Others must patiently practice. The details are given in the Bioelectronics chapter.

You do not have to be an expert in anything to learn the electronic detection method. But a keen sense of hearing helps.

In 1988 1 learned a way to put anything on my skin, blindfolded, and identify it electronically in a few minutes. I could taste something without flavor and identify it electronically. The system worked fine for detecting things in the skin and tongue. Would it be reliable for internal organs, too?

A whole world of discovery lay ahead of me. I wanted to know what was in my inner ear causing tinnitus, in my eyes causing pain, in my stomach causing indigestion and a thousand other things.

But behind the daily excitement of new discoveries, a gnawing question lingered in my mind. How is this possible without some pretty high frequency energy source, radio frequency in fact, running through my circuit? My audio oscillator was only 1000 Hz (hertz, or cycles per second); radio frequency is hundreds of thousands of Hz. And the phenomenon could be produced with an old-fashioned dermatron', too, that only puts out DC (direct current)-no frequencies at all!

A high frequency energy had to be coming from somewhere. Was it me? Ridiculous!

But there was a way to test. If my own body was putting forth the high frequency energy, it could be bled off and diverted into the ground with a correct size capacitor. This should stop the feedback oscillations. This turned out to be true; it was stopped. But ridiculous kept ringing in my ears and I tried an

1The dermatron was invented decades ago and made famous by Dr. Voll. Establishment science disdained it!

other test. If there was indeed radio frequency (RF) running through my circuit I should be able to block it with the right snap-on choke. It did block. I thought of a third test. If this was truly a resonance phenomenon I should be able to add a capacitance to this circuit and see the resonance destroyed. Then add an inductance and see the resonance return. It did just that. I made graphs of the relationship between capacitance and inductance. They were entirely reproducible.

Then why couldn't I see the RF on my RIF oscilloscope? Probably because it was high frequency energy, not high energy frequency, and I didn't know how to amplify it above the background noise level. It was nevertheless not convincing. Yet much too tantalizing to ignore.

I thought of yet a fourth test. If I was really producing RF radiation that could be channeled through a circuit, I should be able to interfere with it by adding another RIF radiation from an outside source. I added a frequency from my frequency generator, first at 1,000 Hz. Now there was no resonance. It interfered. Did this mean that my body was not producing radiation at 1,000 Hz? Or was my 1,000 Hz radiation being matched and canceled? I raised the frequency gradually, from 1,000 to 10,000 to 100,000 to 1,000,000 Hz. There was no resonance anywhere, and I couldn't draw any conclusions. It was 5 o'clock on Sunday afternoon. Quitting time. But one last look at my generator reminded me that it could reach 2,000,000 Hz and I was just at 1,000,000. One more quick experiment wouldn't take much time. I cranked it to 1,800,000 Hz. And now a resonance screamed out! Was I "hearing things?" No more interference. I did it over and over. Why was it resonating now and not before? Had I arrived at my body's own bandwidth (transmission range), and this was the reason it no longer interfered?

I found the lowest frequency that resonated to be 1,562,000 Hz. All frequencies that I checked (about 2,000) from there up to 2,000,000 (my frequency generator would go no higher) also resonated.

A year later I purchased a better frequency generator to search for the upper end of my bandwidth. Any frequency between 1,562,000 and 9,457,000 Hz could be added to the circuit and produce resonance. It seemed obvious, then, that the human body broadcasts electrically, just like a radio station, but over a wide band of frequencies and very low voltages, which is why it has not been detected and measured until now.

It was a busy year, now 1989. 1 was determined to find a bandwidth for other living things: I found them for flies, beetles, spiders, fleas, ants. They were between 1,000,000 Hz and 1,500,000 Hz; cockroaches were highest amongst insects I tested.

Then came a dismaying finding. A dead insect had a bandwidth too! Much narrower, and near the top end of the same range it had when living, but distinctly present. So it wasn't altogether a living phenomenon.

But if dead things had a resonant bandwidth, then maybe a prepared microscope slide of a dead creature could be used, and my trips to the garden and telephone calls to abattoirs (for meat parasites) could cease. That was a lucky thought. My first slide was of the human intestinal fluke, a huge parasite, scourge of humanity. I had just found it to be present in the liver (not intestine) of every cancer sufferer I saw. The (dead) adult parasite had a resonant frequency around 434,000 Hz. Slides of that parasite's redia resonated nearby (432,000 Hz), as did its other stages.

Dead things still resonated! The entire catalog of biological supply companies, hundreds of specimens of viruses, bacteria, parasites, molds, and even toxins, were now available to research with this new technique!

Suddenly an idea bolted out of the blue. If a person were to hold on to the frequency generator while it was generating 434,000 Hz, what would happen to the adult fluke, if you were infected with it?

I tested this plan that same week on myself, not with the fluke but with Salmonella bacteria and Giardia and Herpes that I carried chronically. After a 3 minute treatment, I retested myself. I could no longer find them in my organs! There were no emissions at their characteristic frequencies. I repeated and repeated. Were they really dead? Maybe they were just numbed or were suddenly hiding. But symptoms were gone quickly too. My Herpes lesion stopped tingling. It was all too simple and unbelievable.

But was it safe? Within three weeks I had reliable data regarding the necessary level of electrical treatment. It only took 5 volts for three minutes at the specific frequency. It is not as if you had to use house current which would kill you, along with the parasite.

In twenty minutes (three minutes at six different frequencies) a whole family could get rid of this parasite. Cancer cases showed that in a few hours the universal cancer marker, orthophospho-tyrosine could be banished from their bodies by killing this same parasite.

"Incurable" HIV cases lost their virus in a few hours, too. Laboratory retesting for HIV came back negative! Most cases of pain got immediate relief if I could identify the correct "bug" and have its frequency found by the next office visit. This seemed to be absolute proof that living things had an essential high frequency output of some kind of energy.

What was actually happening to the bacteria or parasites? If I could kill something as large as an Ascaris worm or intestinal fluke, then perhaps I could kill something even larger, like an earthworm or flea, something I could see with my own eyes instead of having to imagine its demise inside my body.

Ten minutes at a :frequency chosen near the top of their broadcast range seemed to anesthetize them. But they didn't die. Later I checked the body bandwidth (the range of frequencies they emit) of each. The earthworms had lost a lot of their bandwidth, both at the top and bottom. The fleas seemed hardier; they had only lost a little. However they did not recover, even weeks later, from this loss.

Could it harm humans to douse them with RF frequencies in their own bandwidth? Quite probably, if the voltage were high enough. There was no need to experiment, though, because the parasites we want to kill have characteristic frequencies that do not overlap the characteristic frequencies of a human. In fact, they are far away (see the chart on page 17).

So my electronic method attacking illness was born. Find the resonant frequency of a bacterium, virus or parasite using a slide or dead bit. Treat the living invaders inside the human body with this frequency and in a matter of minutes they are no longer transmitting their own bandwidths-they are dead or sick and will be removed by our white blood cells.

It was a worrisome truth. Perhaps the department of defense would use this knowledge and develop super high voltage devices to kill people ("enemies") somewhere in the world. But I couldn't let sick people suffer. Besides, it would probably require a voltage much like lightning to kill people from a distance. Possibly a way could be found to shield yourself from frequencies harmful to humans by wearing a choke (inductor) coil which suppresses these frequencies. Remember, there was no recovery, just a slow death for my experimental animals. It must not happen to humans!

Meanwhile, people must be alerted that they can safely kill their invaders and heal their chronic illnesses. Invaders that have been increasing exponentially due to lowered immunity in recent decades. Possibly this is true for all species on our planet. The pollution of the entire biosphere has been increasing and with it the prospect of acquired immune deficiency syndrome (AIDS) for all of us.

Remember, though, that the true challenge is not to kill our invaders but to regain our health and immunity.

More than just parasites are making us sick! Pollution is too. Selective electrocution rarely makes people completely well. Sick people always have an environmental factor that must be corrected also.

How do we do that? The ship of "progress", of increasingly complex, processed foods and products, must be turned around and simplicity become our goal. Survival is in simplicity of food intake, simplicity of life habits. Did Ralph Waldo Emerson foresee this when he said "To be simple is to be great"? Or will daily parasite and pathogen electrocution become another crutch that makes us just enough better that we can continue a detrimental lifestyle? Yet another "Band-Aid" treatment for our poisoned planet?

Strange as it appears, it now seems obvious that every living creature broadcasts its presence like a radio station, the sun, or the stars. I have named it bioradiation.

Perhaps it is the same energy as the Asian chi; perhaps it is merely related to it. Perhaps it is the energy that runs along the meridians discovered eons ago by Asian practitioners.

Perhaps it is the energy that faith healers and religious teachers know how to harness, perhaps not.

Perhaps it is the energy that psychics perceive and that drives occult phenomena, perhaps not.

What is truly amazing is that ordinary persons have discovered such energy well ahead of scientists. Persons using the cc art" of kinesiology, pendulums, radionics, dousing rods and many other forms of "strange energy" have no doubt harnessed a part of this bioradiation. It is a tribute to the generally high intelligence of common people and to their open-mindedness that they discovered this energy, in spite of opposition from scientists of today.

Over a century ago the scientists of Europe proposed the existence of a "life force" called "elan vitale." They were scorned out of existence (and out of jobs). Young scientists, (including myself) were systematically taught to scorn this idea. Of course we were also taught that a good scientist was unemotional, does not scorn ideas, has a completely open mind, and does not rule something out until it is disproved to their satisfaction. The youthfulness of college years is so susceptible to prejudices of all kinds, and the desire for acceptance is so great, that special effort needs to be made to teach neutrality. Or at least to distinguish between emotion and fact. Where have these basic pedagogic principles gone? I was indeed inspired with the phrase "search for truth" but then promptly led down the path of " search for acceptance."

I do not know what bioradiation, this electrical broadcast from our cells, is made of Only its frequency was noticed and caught (modulated) in such a way as to be measurable. And this frequency, 1,520,000 to 9,460,000 Hz (for a human infant) is in the radio frequency (RF) range2.

By zapping I mean selectively electrocuting pathogens. For years I used a commercial frequency generator to "zap" one pathogen after another.

First I made a chart of the frequencies for most of the bacteria and viruses in my collection (over 80, see page 561). Then I would test the sick client for each one of these, and hope they did not have one for which I didn't have a sample. Even persons with a simple cold typically had a dozen they tested positive to (not just A denovirus).

Next it was time to tune in the frequency generator to a dozen frequencies for three minutes each. The total process, testing and treatment, would take about two hours. They frequently got immediate relief But often the relief would be temporary. What I didn't know at that time was that viruses could

2 AM radio broadcasts are from 540,000 Hz to 1,600,000 Hz (slight overlap with lower end of human band), FM is 88,000,000 to 108,000,000 Hz (out of the human range). infect a larger parasite such as a roundworm. Until you killed your roundworm and your virus, you would keep getting the virus back promptly.

In 1993 my son, Geoffrey, joined me and we tried a new approach. He programmed a computer controlled frequency generator to automatically cover all the frequencies populated by all the parasites, viruses, and bacteria, from 290,000 Hz to 470,000 Hz. It spent about three minutes for every 1000 Hz it covered. This was more efficient, but it meant spending Len hours being zapped.

Again, the results were disappointing. Arthritis pain, eye pain, colds were improved, but not completely cured overnight. Months later I would find that organisms were transmitting as low as 170,000, and as high as 690,000 Hz. My specimen collection was obviously incomplete. To cover this larger range, spending three minutes for every 1000 Hz, would take 26 hours. Still worth doing if it would indeed help all our illnesses. But even this method of zapping was not 100% effective for reasons yet to become clear.

In 1994 my son built a hand held, battery operated, accurate frequency generator. The purpose was to enable everyone to kill the intestinal fluke at 434,000 Hz with a low cost device. Enough benefit would be derived from zapping at various frequencies that I thought everyone should know how to make one. When I tested it on one of my own bacteria, however, three others at much different frequencies died also! This had never happened before. When I tested it on others, even though they had dozens of pathogens, all were killed!

Subsequent testing showed it was not due to some unique design, or special wave form produced by the device. It was due to battery operation!

Any positively offset frequency kills all bacteria, viruses and parasites simultaneously

given sufficient voltage (5 to 10 volts), duration (seven minutes), and frequency (anything from 10 Hz to 500,000 Hz).

Before this I had always set my commercial frequency generator to alternate between positive and negative voltage. Now I tried setting it to alternate between positive and zero voltage (positive offset). It was just as effective as the battery operated frequency generator my son designed.

Generating positive offset frequencies is the best way to kill all pathogens quickly.

But it takes more than one treatment.

It takes three treatments to kill everything. Why? The first zapping kills viruses, bacteria and parasites. But a few minutes later, bacteria and viruses (different ones) often recur. I conclude they had been infecting the parasites, and killing the parasites released them. The second zapping kills the released viruses and bacteria, but soon a few viruses appear again. They must have been infecting some of the last bacteria. After a third zapping I never find any viruses, bacteria or parasites, even hours later.

Why didn't the virus inside the parasite die with the first zapping? It may be because electricity travels on the exterior of things. The body of the parasite shielded the interior. This is why my earlier, promising work spending hours on a frequency generator gave only partial or temporary improvement-it was only done once, not three times. And it explains why a single treatment with a frequency generator or zapper frequently gives you a cold!

Zapping does not kill shielded organisms

Fig. I Selected animal bandwidths.

Fig. 2 Selected pathogen bandwidths.

Applying an alternating electrical voltage within an organism's bandwidth injures it. Small organisms with narrow bandwidths are extinguished quite readily (three minutes at five volts).

Positively offset frequencies can kill the entire range of small organisms (viruses, bacteria, parasites) in just seven minutes.

Building A Zapper

Being able to kill your bacteria and other invaders with electricity becomes much more of a panacea when you can do it all in three 7 minute sessions. No need to single out specific frequencies or to sweep through a range of frequencies one KHz at a time. No matter what frequency it is set at (within reason), it kills large and small invaders: flukes, roundworms, mites, bacteria, viruses and fungi. It kills them all at once, in 7 minutes, even at 5 volts.

How does it work? I suppose that a positive voltage applied anywhere on the body attracts negatively charged things such as bacteria. Perhaps the battery voltage tugs at them, pulling them out of their locations in the cell doorways (called conductance channels). But doorways can be negatively charged too. Does the voltage tug at them so they disgorge any bacteria stuck in them? How would the positive voltage act to kill a large parasite like a fluke? None of these questions can be answered yet.

Other fascinating possibilities are that the intermittent positive voltage interferes with electron flow in some key metabolic route, or straightens out the ATP molecule disallowing its breakdown. Such biological questions could be answered by studying the effects of positive frequencies on bacteria in a lab.

The most important question, of course, is whether there is a harmful effect on you. I have seen no effects on blood pressure, mental alertness, or body temperatures. It has never produced pain, although it has often stopped pain instantly. This does not prove its safety. Even knowing that the voltage comes from a small 9 volt battery does not prove safety, although it is reassuring. The clotting of red blood cells, platelet aggregation and functions that depend on surface charges on cells need to be investigated. But not before you can use it. Your safety lies in the short period of exposure that is necessary. Viruses and bacteria disappear in 3 minutes' tapeworm stages, flukes, roundworms in 5; and mites in 7. One need not go beyond this time, although no bad effects have been seen at any length of treatment.

The first seven minute zapping is followed by an intermission, lasting 20 to 30 minutes. During this time, bacteria and viruses are released from the dying parasites and start to invade you instead.

The second seven minute session is intended to kill these newly released viruses and bacteria. If you omit it, you could catch a cold, sore throat or something else immediately. Again, viruses are released from the dying bacteria. The third session kills the last viruses released.

Do Not Zap If You Are Pregnant

Or Wearing A Pacemaker.

These situations have not been explored yet. Don't do these experiments yourself Children as young as 8 months have been zapped with no noticeable ill effects. For them, you should weigh the possible benefits against the unknown risks.

That is all there is to it. Almost all. The zapping current does not reach deep into the eyeball or testicle or bowel contents. It does not reach into your gallstones, or into your living cells where Herpes virus lies latent or Candida fungus extends its fingers. But by zapping 3 times a day for a week or more you can deplete these populations, too, often to zero.

Killing The Surviving Pathogens

The interior of gallstones may house parasites inaccessible to the zapping. Eliminate this source of reinfection by flushing them out with liver cleanses (page 552).

Although the center of the bowel contents is often unaffected by electric current, which lets bowel bacteria like Shigella, Escherichia coli (E. coli) and parasite stages survive, sometimes it is nearly all sterilized by zapping. This results in considerable shrinkage of the bowel movement. Eliminate remaining parasites and bacteria with a single dose (2 tsp.) of Black Walnut Hull Tincture, Extra Strength (see page 543).

There is no way of distinguishing between "good" and "bad" bacteria with either of these methods. However even good bacteria are bad if they come through the intestinal wall, so zapping targets mostly "bad" bacteria. The good news is that perfect bowel habits often result in a few days. Evidently, the good bacteria are benefited by killing the invasive ones. Homemade yogurt and buttermilk (see Recipes) are especially good at recolonizing the bowel. But it does not seem wise to culture yourself with special commercial preparations and risk getting parasite stages again when you can become normal so soon anyway. If you do decide to take some acidophilus bacteria to replenish your intestinal flora make sure you test for parasites like Eurytrema first.

When a large number of parasites, bacteria and viruses are killed, it can leave you fatigued. Try to give yourself a lowstress day after your initial zapping. But there are no significant side effects. I believe this is due to the second and third zapping which mops up bacteria and viruses that would otherwise be able to go on a feeding frenzy with so much dead prey available.

To build your zapper you may take this list of components to any electronics store (Radio Shack part numbers are given for convenience).

Zapper Parts List
Item Radio Shack Catalog Number large shoe box 9 volt battery
9 volt battery clips 270-325 (set of 5, you need 1)
On-Off toggle switch 275-624A micro mini toggle switch
1 KOhm resistor 271-1321 (set of 5, you need 2)
3.9 K Ohm resistor 271-1123 (set of 2, you need 2)
low-current red LED 276-044 or 276-041 or 276-045
.0047 uF capacitor 272-130 (set of 2, you need 1)
.01 uF capacitor 272-1065 (set of 2, you need 1)
555 CMOS timer chip 276-1723 (set of 2, you need 1)
8 pin wire-wrapping socket for 276-1988 (set of 2, you need 1) Note: Radio
the chip Shack is discontinuing all wire wrap sockets. Find
another parts store or use 276-1995 (but the legs
are much shorter and harder to attach clips to).
short (12") alligator clip leads any electronics shop, get 6
Microclip test jumpers 278-017 (you need 2 packages of 2)
2 bolts, about 1/8" diameter, 2" hardware store
long, with 4 nuts and 4 washers
2 copper pipes, 3/4" diameter, 4" hardware store
long
sharp knife, pin, I
Hints for absolute novices: Don't let unusual vocabulary deter you. A "lead" is just a piece of wire used to make connections. When you remove a component from its package, label it with a piece of tape. A serrated kitchen knife works best as does a large safety pin. Practice using the microclips. If the metal ends are L-shaped bend them into a U with the long-nose pliers so they grab better. Chips and chip holders are very fragile. It is wise to purchase an extra of each in case you break the connections.

Give this to an electronics person or make it yourself in a shoebox by using the following instructions.

Resistor color 1K=Brown-Black-Red-(tolerance-typically gold,silver,or red) 3.9K=Orange-White-Red-(tolerance)
Fig. 3 Zapper schematic. Assembling The Zapper

1. You will be using the lid of the shoe box to mount the components. Save the box to enclose the finished project.
2. Pierce two holes near the ends of the lid. Enlarge the holes with a pen or pencil until the bolts would fit through. Mount the bolts on the outside about half way through the holes so there is a washer and nut holding it in place on both sides. Tighten.
Label one hole "grounding 0 Gro 0 ding Bolt bolt" on the inside and outside.
3. Mount the 555 chip in the wire wrap socket. Find the "top end" of the chip by searching the outside surface carefully for a cookie-shaped bite or hole taken out of it.
Align the chip with the socket and very gently squeeze the
pins of the chip into the socket until they click in place.
4. Make 8 pinholes to fit the wire wrap socket. Enlarge them slightly with a sharp pencil. Mount it on the outside. Write in the numbers of the pins (connections) on both the outside and inside, starting with number one to the left of the "cookie bite" as seen from outside. After number 4, cross over to number 5 and Bolt Grounding Bolt continue. Number 8 .0 will be across from number 1.
5. Pierce two holes 1/2 inch apart very near to pins 5, 6, 7, and 8. They should be less than 1/8 inch away. (Or, one end of each component can share a hole with the 555 chip.) Mount the .01 uF ca The other handhold is attached to the other bolt. Connect the scope ground wire to one end of the resistor. Connect the scope probe to the other end of the resistor. Turn the zapper ON and grasp the handholds. Read the voltage on the scope. It will read about 3.5 volts. Calculate current by dividing voltage by resistance. 3.5 volts divided by I KOhm is 3.5 ma (milliamperes). 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 7 minutes, let go of the handholds, turn off the zapper, and rest for 20 minutes. Then 7 minutes on, 20 minutes rest, and a final 7 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 (see Lesson Twelve, page 492, or Lesson Twenty Seven, page 509). This gives you a starting point. Then zap yourself. After the triple zapping, none of these invaders should be present.

Simple Purser

If you are ill or want a reliable zapping, make the first model. However, there is another way to make a zapper if you can not afford to build the first model.

An ordinary battery is a source of positive voltage. It is the positive voltage that eliminates so many parasites at once, not a specific frequency. So although the zapper's frequency is about 30 kHz (thirty thousand "zaps" per second), even 5 Hz (five "zaps" per second), about as fast as you can tap the battery with your hand, is moderately effective!

You must be connected to both terminals. One will be marked + (positive) and the other - (negative). If you simply touch these terminals with your wet fingers, nothing much happens. That is because your resistance to the current starts going up right away, so less and less current passes through you.

Fig. 5 Simple pulser.

However if you Lap the positive terminal with your wet hand, and tap it at a fairly high rate, your body's capacitors come into play. Capacitors only take part in the flow of electricity when they are charged and discharged. Tapping the terminal starts and stops the voltage so capacitors charge and discharge. This kind of resistance to current flow is much smaller.

The faster you tap, the greater the frequency of current pulses and the lower this kind of resistance becomes. Now you can have a considerable sustained current flow through your body.

If you can tap even twice per second (2 Hz) for ten minutes without interruption you can give yourself a zapping that is moderately effective. Remember to take an intermission of twenty minutes and then repeat to avoid catching new viruses. After a second twenty minute intermission repeat zapping a third time.

Using The Simple Pulser
1. Wrap each handhold with 9 volt battery one layer of wet paper 2 short (12") alligator clip leads (from towel. Place each on a any electronics shop)
2 copper pipes, 3/4" diameter, 4" long non-conductive surface, (from a hardware store) like a plastic bag.

2. Connect the positive battery terminal to one handhold and the negative terminal to the other handhold using alligator clip leads.

3. Don't let the handholds touch.

4. Place a clock in front of you to time yourself.

5. Pick up the right handhold with your right hand.

6. Leave the left handhold on the table. Tap it with your left hand, preferably the fleshy part of the palm. You may brace yourself with your fingers on the plastic. Keep up a steady pace as fast as you are able.

7. When you get tired pick up the left handhold with your left hand and tap with your right hand. Keep changing off with the least interruption.

8. Repeat a second time 20 minutes later, and a third time 20 minutes after that.

A single 9 volt battery will wear out rather quickly used this way. Put two together, in' parallel, for longer lasting power. This requires two more short alligator clips. Connect positive terminals of the batteries to each other, and the negatives also.

Making A Syncrometer

This is an audio oscillator circuit in which you include yourself by means of a handhold. You listen to the current in your circuit with a loudspeaker. Other oscillator circuits will work, too. A lot of fascinating opportunities present themselves with this concept.
I have previously published three ways to build the Syncrometer circuit.35 Here is the circuit diagram:

4700pf moly cap .1 mfd 16v cap 2N2907 PNP min output transf 8-90OU 150 .25w res 3 AA batteries speaker (like RadioShack 277-1008C)

Fig. 79 Syncrometer schematic.

If you are not an electronics enthusiast, you can still assemble a Syncrometer using a hobby kit. No soldering is required. Here is what you need:

Making a Hobby Kit Syncrometer
Item Radio Shack Cat. No.
200 in One Electronic Project Lab by 28-262
Science Fair
3 AA 1 1/2 volt batteries
  35In The Cure for all Cancers and The Cure for HIV/AIDS.

Alligator clip test jumpers You need 2. Handhold. A four inch length of 3/4 inch copper pipe, like for plumbing.
These dimensions are critical to assure maximum skin contact.
Probe. A banana plug. Precision Mini-Hook Test Lead Set (contains two, you only need one)- 278-1160A
Pencil, new.

Pig. 80 Syncromer parts list.

Build The Electrosonic Human in the 200 in One Electronic Project Lab. It takes about 10 minutes.

Later, when you use the probe to press against your knuckle you may find getting the right sound is painful. In this case try substituting the .005 microfarad capacitor for the .01 microfarad capacitor in the circuit.

Attach the Probe. The Archer Precision Mini-Hook Test Lead Set has a banana plug for the probe on one end and a minihook on the other end for easy attachment to the circuit. Tape a long, new pencil to the probe to make it easier to hold. Connect the Probe to middle post of the primary side of the transformer (it also connects to the negative battery post). You will not be using the two connections the instuctions tell you to hold.

Attach the Handhold. Clip the Handhold to one end of an alligator clip test jumper, and clip the other end to the base (B) of the transistor used in the circuit.

Attach an alligator clip to the post of the transformer that connects to the two capacitors. This will go to the test plates.

Final test. Turn the control knob on and keep turning the potentiometer to nearly the maximum. (This reduces the resistance. The schematic has a 150 ohm fixed resistor in place of the potentiometer.) Make sure you have good batteries installed. Test the circuit by briefly touching the Probe to the Handhold. The speaker should produce a sound like popping corn. If it does not, check that your alligator clips are not bending the spring terminals so much that other wires attached there are loose. Finally, turn switches OFF.

Making Test Plates

This is the box you attach to the basic Syncrometer circuit. It has test plates to put your test substances and tissue samples on. The wiring in it is arranged so that you can test for a toxin in a product, as well as search in yourself This means you can search for Salmonella in the milk or cheese you just ate, not just for Salmonella in your stomach.

Only if the resonant frequency of an item on one plate is equal to the resonant frequency of an item on the other plate will the entire circuit oscillate or resonate! This implies the two plates have something in common. By putting a known pure sample on one plate you can reliably conclude the other sample contains it if the circuit resonates.

You may build a test plate box into a cardboard box (such as a facial tissue box) or a plastic box. Here are the instructions for the cardboard box model.

Stiff paper.
Aluminum foil.

A facial tissue box is easiest. A plastic project box, about 7" x 4" x 1 1/2," makes a more durable product, but requires a drill, and you should discard any metal lid it comes with.

3 bolts (tapered heads) about I inch long, 1/8 inch diameter and 6 washers and nuts to fit.

toggle switch with OFF-ON positions. Alligator clip test leads.

Test Plates Assembly

Cut two 3-1/2 inch squares out of stiff paper such as a milk carton. Cover them with 4 1/2 inch squares of aluminum foil, smoothed evenly and tucked snugly under the edges. You have just made yourself a set of open capacitors. Turn the box upside down and draw squares where you will mount them at the ends of the box. Don't actually mount them, to save wear and tear on them, until the rest of the box is complete.

Mount the ON OFF switch on the front of the box, underneath the right hand plate. Line it up so ON is downward and OFF is up. (An electronics shop can determine this for you at the time of purchase.) Label the box with ON and OFF signs.

Two bolts will be reserved for the plates. The third bolt is used as a terminal where the current from the oscillator circuit will arrive. Make a hole on the side of the box, near the left hand plate and mount the bolt so it sticks half way inside and halfway outside the box. It does not matter whether the head is inside or outside. Tighten it there with a nut on each side of the box. Label it TERMINAL. It merely means connecting place.

Mark the center of each square that you drew and each capacitor you built. Pierce first with a pin; follow with a pencil until a round hole is made at the center. Mount each plate with a bolt, fastening it below with a nut. Washers are optional.

The left side connection (terminal) gets attached to the left plate (bolt) with an alligator clip. Use another clip to attach the same left plate (bolt) to the ON OFF switch (there are two connections, use either one). Finally attach the ON OFF switch connection you didn't use to the right plate (bolt). Make sure the connections at the switch are not touching each other; you might tape them to guard against this.

All these connections should be checked carefully to make sure they are not touching others accidentally. But if you leave the box open so you can see any problems and use clear tape around connections to prevent accidental touching to the wrong connection, it should work OK.

Finally, trace your current. It comes in from the Syncrometer at the main terminal on the left. It is brought to the left plate. When the switch is ON it is simultaneously brought to the right plate. Notice that the plates are not connected to anything else. They are simply capacitors, letting current in and out momentarily and at a rate that is set by the frequency of the oscillator circuit, about 1,000 hertz. This frequency goes up as the resistance (of the circuit or your body ) goes down.

The probe and handhold allow you to include yourself in the Syncrometer circuit. You grasp these when testing. This makes you part of the circuit.

The speaker lets you "listen" to the current. As resistance drops, current goes higher and frequency goes up. As frequencies go higher in the circuit, pitch goes higher. You will be comparing the sound of a standard "control" current with a test current.

Using The Syncrometer

Fill a saucer with cold filtered tap water. Fold a paper towel four times and place it in this dish. It should be entirely wet.

Cut paper strips about I inch wide from a piece of white, unfragranced, paper towel. Dampen a paper strip on the towel and wind it around the copper pipe handhold to completely cover it. The wetness improves conductivity and the paper towel keeps the metal off your skin.

* Start with the test plate switch at OFF.

· Turn the control knob (potentiometer) on, and to near maximum.

Touch each plate with the probe, while holding the copper pipe with one hand. Only the left plate should give you a sound from the speaker. Turn the test plate switch ON. Now both plates should give you a sound when the probe touches them.

Turn the test plate switch OFF again.
Pick up the handhold, squeeze it free of excess water.

Pick up the probe in the same hand, holding it like a pen, between thumb and forefinger.

Dampen your other hand by making a fist and dunking your knuckles into the wet paper towel in the saucer. You will be using the area on top of the first knuckle of the middle finger or forefinger to learn the technique. Become proficient with both. Immediately after dunking your knuckles dry them on a paper towel folded in quarters and placed beside the saucer. The degree of dampness of your skin affects the resistance in the circuit and is a very important variable that you must learn to keep constant. Make your probe as soon as your knuckles have been dried (within two seconds) since they begin to air dry further immediately.

With the handhold and probe both in one hand press the probe against the knuckle of the other hand, keeping the knuckles bent. Press lightly at first, then harder, taking one half second. Repeat a half second later, with the second half of the probe at the same location. There is an additive effect and you get two chances to listen to the current. All of this takes less than two seconds. Don't linger because your body will change and your next probe will be affected.

Subsequent probes are made in exactly the same way. As you develop skill, your probes will become identical. Plan to practice for one or two hours each day. It takes most people at least twelve hours of practice in order to be so consistent with their probes that they can hear the slight difference when the circuit is resonant.

For reference you may wish to use a piano. The starting sound when you touch down on the skin should be F, an octave and a half above middle C. The sound rises to a C as you press to the knuckle bone, then slips back to B, then back up to Csharp as you complete the second half of your first probe. If you have a multitester you can connect it in series with the handhold or probe: the current should rise to about 50 microamps. If you have a frequency counter the frequency should reach 1000 Hz. You should arrive at C-sharp just before the probe becomes painful.

Two things change the sound of the probes even when your technique doesn't change.

1. The patch of skin chosen for probing will change its properties. The more it is used, the redder it gets and the higher the sound goes when you probe. Move to a nearby location, such as the edge of the patch, when the sound is too high to begin with, rather than adjusting the potentiometer.

2. Your body has cycles which make the sound go noticeably higher and lower. If you are getting strangely higher sounds for identical probes, stop and only probe every five minutes until you think the sound has gone down to standard. This could take five to twenty minutes. Learn this higher sound so you can avoid testing during this period.

You may also find times when it is impossible to reach the necessary sound without pressing so hard it causes pain. You may adjust the potentiometer if that helps.
All tests are momentary.

This means less than one second. It is tempting to hold the probe to your skin and just listen to the sound go up and down, but if you prolong the test you must let your body rest ten minutes, each time, before resuming probe practice!

For our purposes, it is not necessary to locate acupuncture points.

Resonance

The information you are seeking is whether or not there is resonance, or feedback oscillation, in the circuit. If there is the test is YES (positive). You hear resonance by comparing the second probe to the first. You can never hear resonance on the first probe, for reasons that are technical and beyond the scope of this book. You are not merely comparing pitch in the two probes. During resonance a higher pitch is reached faster; it seems to want to go infinitely high.

Remember that more electricity flows, and the pitch gets higher, as your skin reddens or your body changes cycle. These effects are not resonance.

Resonance is a small extra hum at the high end of the probe. As soon as you hear it, stop probing. Your body needs a short recovery time (10 to 20 seconds) after every resonant probe. The longer the resonant probe, the longer the recovery time to reach the standard level again.

Using musical notes, here is a NO (negative result): F-C-B-C# (first probe) F-C-B-C# (compare, it is the same sound). Here is a YES (positive) result: F-C-B-C# (first probe) F-D (stop quickly because you heard resonance). In between the first and second probe a test substance will be switched in as described in lessons below.

It is not possible to produce a resonant sound by pressing harder on the skin, although you can make the pitch go higher. To avoid confusion it is important to practice making probes of the same pressure. (Practice getting the F-C-B-C# tune.)

Making Pure Water for Testing Purposes

Since the water you purchase is likely to have solvents in it and since your tap water may be polluted with heavy metals and since your (or a store's) filtration system may be clogged, it is important to make your own pure water.

Purchase a "filter pitcher" made of hard, opaque plastic, not the clear or flexible variety (see Sources). Fill the pitcher with cold tap water, only, not reverse osmosis, distilled, or any other water, since solvents do not filter out as easily as heavy metals. The filter should be made of carbon only. To make test substances, use fresh water in the pitcher and pour.

If your water has lead, copper or cadmium from corroded plumbing, the filter will clog in five days of normal use. So use this pitcher sparingly, just for making test substances and for operating the Syncrometer.

Lesson One

Purpose: To identify the sound of resonance in the circuit.

Materials: Potentized (homeopathic) solutions. Prepare these as follows: find three medium-sized vitamin bottles, glass or plastic, with non-metal lids. Remove any shreds of paper sticking to the rim. Rinse well with cold tap water. Then rinse again with filtered water.

-Pour filtered water into the first bottle to a depth of about 1/2 inch. Add about 50 little grains of table salt using the tip of a plastic knife. This is a "pinch." Replace the lid. Make sure the

outside is clean. If not, rinse and dry. Now shake hard, holding it snugly in your hand. Count your shakes; shake 120 to 150 times. Use elbow motion so each shake covers about an eight inch distance. Shaken samples are different from unshaken ones, that's why this is so important. When done label the bottle on its side and lid: SALT # 1. Wash your hands (without soap).

Next, pour about the same amount of filtered water into the second and third bottles. Open SALT #1 and pour a small amount, like 1/4 to 1/2 of a teaspoon (do not use a spoon) into the second and third bottles. Close all bottles. Now shake the second bottle the same as the first. Clean it and label it SALT #2. Do the same for the third bottle. Label it SALT #2 also and set aside for Lesson Four.

These two solutions have unique properties. SALT 4 1 always resonates. Use #1 to train your ear. SALT 42 shouldn't resonate. Use #2 to hear when you (your body's internal resistance) have returned to the standard level.

Turn the Syncrometer ON.

Place the SALT #2 bottle on the right test plate.

Start with the plate switch OFF.

Make your first probe (F-C-B-C#).

Flip the plate switch ON, taking only one half second. Brace your hand when switching so it is a fast, smooth, operation.

Make the second probe (F-C-B-C#). Total probe time is 2 1/2 seconds. Count it out, "a thousand and one (done with first probe) a thou. (done with switching) a thousand and one (done with second probe)."

7. The result should be a NO (negative). If the second probe sounds even a little higher you are not at the standard level. Wait a few more seconds and go back to step 3.

8. If the first result was NO, remove SALT #2 and put SALT 41 on. Put the test plate switch back to OFF and repeat the test. This time the circuit was resonating. Learn to hear the

difference between the last two probes so that a resonant probe can be terminated early (reducing rest time).

9. The skin must now be rested. When SALT #1 is placed in the circuit there is always resonance whether you hear it or not. Therefore, always take the time to rest the skin.

10. How can you be sure that the skin is rested enough? Any time you want to know whether you have returned to the standard level, you may simply test yourself to SALT #2 Oust do steps 3 through 6). While you are learning, let your piano also help you to learn the standard level (starts exactly at F). If you do not rest and you resonate the circuit before returning to the standard level, the results will become aberrant and useless. The briefer you keep the resonant probe, the faster you return to the standard level. Don't exceed one half second when probing SALT #1. Hopefully you will soon hear resonance within that time.

This lesson teaches you to first listen to the empty plate, then to SALT #2, to check for standard state. Then to compare the empty plate to SALT #1 to check for resonance. In later lessons we assume you checked for your standard level or are quite sure of it.

Practice hearing resonance in your circuit every day.

White Blood Cells

Checking for resonance between your white blood cells and a toxin is the single most important test you can make.

Your white blood cells are your immune system's first line of defense. In addition to making antibodies, interferon, interleukins, and other attack chemicals, they also "eat" foreign substances in your body and eliminate them. By simply checking your white blood cells for toxins or intruders you save having to check every other tissue in your body. Because no matter where the foreign substance is, chances are some white blood cells are working to remove it.

It took me two years to find this ideal indicator, but it is not perfect. Tapeworms are a notable exception. They can be encysted in a particular tissue which will test positive, while the white blood cells continue to test negative. Also, when bacteria and viruses are in their latent form, they do not show up in the white blood cells. Fortunately, in their active form they show up quite nicely. Freon is an example of a toxin that is seldom found in the white blood cells; but typically, the white blood cells are excellent indicators of toxins.

Making a White Blood Cell Specimen

Obtain an empty vitamin bottle with a flat plastic lid and a roll of clear tape. The white blood cells are not going into the bottle, they are going on the bottle. The bottle simply makes them easy to handle. Rinse and dry the bottle. Make a second specimen on a clean glass slide if available. Squeeze an oil gland on your face or body to obtain a ribbon of whitish matter (not mixed with blood). Pick this up with the back of your thumb nail. Spread it in a single, small streak across the lid of the bottle or the center of the glass slide. Stick a strip of clear tape over the streak on the bottle cap so that the ends hang over the edge and you can easily see where the specimen was put (see photo). Wipe the lid beside the tape to make sure all white blood cells are covered. For the Slide, apply a drop of balsam and a cover slip (see Sources). Both types of preparation will give you identical results. The bottle type of white blood cell specimen is used by standing it on its lid (upside down) so that the specimen is next to the plate. The lid is used because it is flat, whereas the bottom of most bottles is not.
Lesson Four

Purpose: To determine your percent accuracy in listening for resonance.

Materials: The SALT #1 and SALT #2 solutions you made for Lesson One.

Method: Move the SALT #1 and SALT #2 labels to the bottom of the bottles so you can not tell which bottle is which.

I . Turn the Syncrometer ON.

2. Start with the test switch OFF.

3. Mix the bottles up, select one at random, and place it on the right plate.

4. Listen to the current.

5. Flip the plate switch ON and make your second probe.

6. Resonance indicates a SALT #1, no resonance indicates SALT #2. Check the bottom. Remember to rest after the SALT # 1, whether or not you heard resonance.

7. Repeat steps 3 through 5 a number of times. Work toward getting three out of three correct. Practice every day.

Trouble shooting:

a) If you repeat this experiment and you keep getting the same bottles "wrong", start over. You may have accidentally contaminated or mislabeled the outside of the bottle, or switched bottle caps.

b) If you get different bottles wrong each time, the plates may be contaminated. Wash the outside of the bottles and rinse with filtered water and dry. Wipe the plates very gently too, with filtered water and dry. Or replace the plates.

c) If all the bottles read the same, your filtered water is polluted. Change the filter.
Preparing Test Substances

It is possible to prepare dry substances for testing such as a piece of lead or grains of pesticide. They can simply be put in a plastic bag and placed on the test plate. However, I prefer to place a small amount (the size of a pea) of the substance into a 1/2 ounce bottle of filtered water. There will be many chemical reactions between the substance and the water to produce a number of test substances all contained in one bottle. This simulates the situation in the body.
 

Within the body, where salt and water are abundant, similar reactions may occur between elements and water. For example, a strip of pure (99.9% pure) copper placed in filtered water might yield copper hydroxide, cuprous oxide, cupric oxide, copper dioxide, and so forth. These may be similar to some of the reaction products one might expect in the body, coming from a copper IUD, copper bracelet or the copper from metal tooth fillings. Since the electronic properties of elemental copper are not the same as for copper compounds, we would miss many test results if we used only dry elemental copper as a test substance.

Impure Test Substances
 

It is not necessary to have pure test substances. For instance, a tire balancer made of lead can be easily obtained at an auto service station. Leaded gasoline and lead fishing weights also make good test substances for lead. There is a disadvantage, though, to using impure test substances. You are including the extra impurities in your test. If your lead object also has tin in it, you are also testing for tin. Usually, you can infer the truth by some careful maneuvering. If you have searched your kidneys for leaded gasoline, fishing weights and tire balancers and all 3 are resonant with your kidneys, you may infer that you have lead in your kidneys, since the common element in all 3 items is lead. (You will learn how to specify a tissue, such as your kidneys, later.)

Using pure chemicals gives you certainty in your results. You can purchase pure chemicals from chemical supply companies (see Sources). Your pharmacy, a child's chemistry set, a paint store, or biological supply company can also supply some.

The biggest repository of all toxic substances is the grocery store and your own home.

You can make test substances out of your hand soap, water softener salt, and laundry detergent by putting a small amount (1/16 tsp.) in a 1/2 ounce glass bottle and adding about 2 tsp. filtered water. (Or for quick testing just put them dry or wet in a sealed plastic baggy.) Always use a plastic spoon.

Here are some suggestions for finding sources of toxic products to make your own toxic element test. If the product is a solid, place a small amount in a plastic bag and add a tablespoon of filtered water to get a temporary test product. For permanent use put it in a small amber glass bottle. If the product is a liquid, pour a few drops into a glass bottle and add about 2 tsp. filtered water. Keep all toxic substances in gla ss bottles for your own safety. Small amber glass dropper bottles can be purchased by the dozen at drug stores (also see Sources). Seal your test bottles with tape for safety and to prevent evaporation.
 

Aflatoxin: scrape the mold off an orange or piece of bread; wash hands afterward.
Acetone: paint supply store or pharmacy.
Arsenic: 1/16 tsp. of arsenate pesticide from a garden shop. A snippet of flypaper.
Aluminum: a piece of aluminum foil (not tin foil) or an aluminum measuring spoon.
lead. (You will learn how to specify a tissue, such as your kidneys, later.)

Using pure chemicals gives you certainty in your results. You can purchase pure chemicals from chemical supply companies (see Sources). Your pharmacy, a child's chemistry set, a paint store, or biological supply company can also supply some. The biggest repository of all toxic substances is the grocery store and your own home. You can make test substances out of your hand soap, water softener salt, and laundry detergent by putting a small amount (1/16 tsp.) in a 1/2 ounce glass bottle and adding about 2 tsp. filtered water. (Or for quick testing just put them dry or wet in a sealed plastic baggy.) Always use a plastic spoon.

Here are some suggestions for finding sources of toxic products to make your own toxic element test. If the product is a solid, place a small amount in a plastic bag and add a tablespoon of filtered water to get a temporary test product. For permanent use put it in a small amber glass bottle. If the product is a liquid, pour a few drops into a glass bottle and add about 2 tsp. filtered water. Keep all toxic substances in glass bottles for your own safety. Small amber glass dropper bottles can be purchased by the dozen at drug stores (also see Sources). Seal your test bottles with tape for safety and to prevent evaporation.

Aflatoxin: scrape the mold off an orange or piece of bread; wash hands afterward.
Acetone: paint supply store or pharmacy.
Arsenic: 1/16 tsp. of arsenate pesticide from a garden shop. A snippet of flypaper.
Aluminum: a piece of aluminum foil (not tin foil) or an aluminum measuring spoon.
Aluminum silicate: a bit of salt that has this free running agent in it.
Asbestos: a small piece of asbestos sheeting, an old furnace gasket, 1/4 inch of a clothes dryer belt that does not say "Made in USA", or a crumb of building material being removed due to its asbestos content (ask a contractor).
Barium: save a few drops from the beverage given clients scheduled for an X-ray. Lipstick that has barium listed in the ingredients.
Benzene: an old can of rubber cement (new supplies do not have it). A tsp. of asphalt crumbs from a driveway.
Beryllium: a piece of coal; a few drops of "coal oil" or lamp oil.
Bismuth: use a few drops of antacid with bismuth in it.
Bromine: bleached "brominated" flour.
Cadmium: scrape a bit off a galvanized nail, paint from a hobby store.
Cesium: scrape the surface of a clear plastic beverage bottle.
CFCs (freon): ask an electronics expert for a squirt from an old aerosol can that used freon as a cleaner. (Squirt into water, outdoors, put the water in a sample bottle.)
Chromate: scrape an old car bumper.
Cobalt: pick out the blue and green crumbs from detergent. A sample of cobalt containing paint should also suffice.
Chlorine: a few drops of pure, old fashioned Clorox,TM
Copper: ask your hardware clerk to cut a small fragment off a copper pipe of the purest variety or a 1/4 inch of pure copper wire.
Ergot: a teaspoon of rye grains, or rye bread. Add grain alcohol to preserve.
Ether: automotive supply store (engine starting fluid).
Ethyl alcohol (grain alcohol): the purest "drinking" alcohol available. Everclear TM in the United States, Protec tm (potable) in Mexico.
Fiberglass: snip a fragment from insulation.
Fluoride: ask a dentist for a small sample.
Formaldehyde: purchase 37% at a pharmacy. Use a few drops only for your sample.
Gasoline: gas station (leaded and unleaded).
Gold: ask a jeweler for a crumb of the purest gold available or use a wedding ring.
Kerosene: gas station.
Lead: wheel balancers from a gas station, weights used on fishing lines, lead solder from electronics shop.
Mercury: a mercury thermometer (there is no need to break it), piece of amalgam tooth filling.
Methanol: paint supply store (wood alcohol).
Nickel: a nickel plated paper clip, a washed coin.
Patulin (apple mold): cut a sliver of washed, bruised apple.
PCB: water from a quarry known to be polluted with it (a builder or electrical worker may know a source).
Platinum: ask a jeweler for a small specimen.
Propyl alcohol: rubbing alcohol from pharmacy (same as propanol or isopropanol). Use a few drops only, discard the rest. Do not save it.
PVC: glue that lists it in the ingredients (polyvinyl chloride).
Radon: leave a glass jar with an inch of filtered water in it standing open in a basement that tested positive to radon using a kit. After 3 days, close the jar. Pour about 2 tsp. of this water into your specimen bottle.
Silicon: a dab of silicon caulk.
Silver: ask a jeweler for a crumb of very pure silver. Silver solder can be found in electronics shops. Snip the edge of a very old silver coin.
Sorghum mold: 1/8 tsp. sorghum syrup.
Styrene: a chip of styrofoam.
Tantalum: purchase a tantalum drill bit from hardware store.
Tin: scrape a tin bucket at a farm supply. Tin solder. Ask a dentist for a piece of pure tin (used to make braces).
Titanium: purchase a titanium drill bit from a hardware store.
Toluene: a tube of glue that lists toluene as an ingredient.
Tungsten: the filament in a burned out light bulb.
Vanadium: hold a piece of dampened paper towel over a gas stove burner as it is turned on. Cut a bit of this paper into your specimen bottle and add 2 tsp. filtered water.
Xylene: paint store or pharmacy.
Zearalenone: combine leftover crumbs of three kinds of corn chips and three kinds of popcorn.

This list gets you off to a good start. Since few of these specimens are pure, there is a degree of logic that you must apply in most cases. If you are testing for barium in your breast, a positive result would mean that a barium-containing lipstick tests positive and a barium-free lipstick is negative.

A chemistry set for hobbyists is a wonderful addition to your collection of test specimens. Remember, however, the assumptions and errors in such a system. A test for silver using silver chloride might be negative. This does not mean there is no silver present in your body; it only means there is no silver chloride present in the tissue you tested.

You are bound to miss some toxins; don't let this discourage you. There is more than enough that you can find.

The most fruitful kind of testing is, probably, the use of household products themselves as test substances. The soaps, colognes, mouthwash, toothpaste, shampoo, cosmetics, breads, dairy products, juices and cereals can all be made into test specimens. Put about 1/8 tsp. of the product in a small glass bottle, add 2 tsp. filtered water and 1/4 tsp. grain alcohol to preserve it. For temporary purposes use a plastic baggy and water only. If you test positive to your household products in your white blood cells you shouldn't use them, even if you can 'not identify the exact toxin.

For a list of toxins and solvents I use, see page 571. To order pure substances see Sources for "chemicals for testing."

Making Organ Specimens

To test for toxic elements or parasites in a particular organ such as the liver or skin, you will need either a fresh or frozen sample of the organ or a prepared microscope slide of this organ. Meat purchased from a grocery store, fresh or frozen, provides you with a variety of organ specimens. Chicken, turkey, beef or pork organs all give the same results. You may purchase chicken gizzards for a sample of stomach, beef liver for liver, pork brains for brain, beef steak for muscle, throat sweet breads for thymus, tripe for stomach lining. Other organs may be ordered from a meat packing plant.

Trim the marrow out of a bone slice to get bone marrow. Scrub the bone slice with hot water to free it of marrow to get a bone specimen. Choose a single piece of meat sample, rinse it and place it in a plastic bag. You may freeze it. To make a durable unfrozen sample, cut a small piece, the size of a pea, and place it in an amber glass bottle (1/2 oz.). Cover with two tsp. filtered water and 1/4 tsp. of grain alcohol (pure vodka will do) to preserve it. These need not be refrigerated but if decay starts, make a fresh specimen.

Pork brains from the grocery store may be dissected to give you the different parts of the brain. Chicken livers often have an attached gallbladder or piece of bile duct, giving you that extra organ. Grocery store "lites" provides you with lung tissue. For kidney, snip a piece off pork or beef kidney. Beef liver may supply you with a blood sample, too. Always wash hands and rinse with-grain alcohol after handling raw meat.

I use 1/2 oz amber glass bottles with bakelite caps (see Sources) to hold specimens. However, plastic bags or other containers would suffice. After closing, each bottle is sealed with a ParafilinTM strip to avoid accidental loosening of the cap. You may use masking tape.

To make a specimen of skin, use hangnail bits and skin peeled from a callous, not a wart. A few shreds will do. Remember, they must be very close to the test plate when in use-, add 2 tsp. filtered water and 1/4tsp. grain alcohol.

Making a Complete Set of Tissue Samples

My original complete set was made from a frozen fish. As it thawed, different organs were cut away and small pieces placed in bottles for preserving in filtered water and grain alcohol. In this way, organs not available from the grocery store could be obtained. The piece of intestine closest to the anus corresponds to our colon, the part closest to the stomach corresponds to our duodenum. The 2 layers of the stomach and different layers of the eye, the optic nerve and spinal cord were obtained this way.

Another complete set of tissue samples were obtained from a freshly killed steer at a slaughter house. In this way the 4 chambers of the heart were obtained, the lung, trachea, aorta, vein, pancreas, and so forth.

Purchasing a Complete Set of Tissue Samples

Slides of tissues, unstained or stained in a variety of ways for microscope study give identical results to the preparations made by yourself in the ways already described. This fact opens the entire catalog of tissue types for your further study. See Sources for places that supply them.
Fig. 82 Some purchased parasite and tissue slides.

You now have a set of organ samples, either fresh, frozen, preserved or on slides. You also have a set of test substances, whether chemical compounds, or elements, or products. Your goal is to search in your own organs and body tissues for the substances that may be robbing you of health.

Keeping yourself healthy will soon be an easy, daily routine.

Body Fluid Specimens

Each of these fluids should be prepared by putting about 1/4 tsp. in a 1/2oz amber glass bottle. Add about 2 tsp. filtered water and 1/4 tsp. grain alcohol for preservation. Undiluted specimens do not work for reasons that are technical and beyond the scope of this book. It is important not to shake the specimen, but to mix gently.

Urine. It is desired to have a pure, uninfected urine sample as a tissue specimen. Since this cannot be proved with certainty, obtain several urine samples from different persons whom you believe to be healthy and make several test specimens in order to compare results. Label your specimens Urine A (child), Urine B (woman), Urine C (mine), and so forth.

Semen. A sample from a condom is adequate. Aged specimens (sent by mail, unpreserved and unrefrigerated) work well also. Use one to ten drops or scrape a small amount with a plastic knife.

Blood. One to ten drops of blood should be used. Clotted or chemically treated blood is satisfactory. A blood smear on a slide is very convenient.

Milk. Cow's milk is too polluted with parasites to be useful. Electronically, a dead specimen is equivalent to a live specimen, so that pasteurization of the milk does not help. A human milk specimen is preferred.

Saliva. Use your own, if you have deparasitized yourself and test negative to various fluke stages. Otherwise find a well friend or child.

Specifying a tissue is the most powerful investigative technique in your arsenal. Any of your tissue samples can be tested for any of your toxic substances.
You Can Now Test Three Different Ways!

When you test with a substance on one plate and nothing on the other, you are searching your entire body for that substance. Such a test is not very sensitive.

By putting a tissue sample on the other plate you are testing for the substance specifically in that tissue, and this is much more sensitive. The tissue need not be the white blood cells. To find mercury in your kidneys you would use a mercury sample on one plate, and a kidney sample on the other. The technique is the same as when you use white blood cells.

If you put a substance on each plate, a resonating circuit means the two samples have something in common. For example, if you have mercury on one plate and some dental floss on the other, a positive result indicates mercury in the floss.

Lesson Five

Purpose: To watch substances travel through your body.

Materials: Prepare a pint of brown sugar solution (white sugar has propyl alcohol pollution) using filtered water. Use about I tsp. brown sugar, 1/8 tsp. vitamin C (to detoxify sorghum mold), and a pint of filtered water. Do not shake it; gently mix. Make a sample bottle by pouring about 1/2 inch into a clean used vitamin bottle. Rinse and dry the outside of the sample bottle. Finally wash your hands with plain water.

Method:

1.Test your skin for the presence of brown sugar, using the newly made sample bottle and your skin specimen. It should not be there (resonate) yet.

2.Prepare a paper applicator by tearing the comer from a white unfragranced paper towel. Fold it to make a wick.

3.Dip the paper wick in the pint of sugar water and apply it to the skin of your inner arm where you can rub freely.  Rub it in vigorously for about 10 seconds (otherwise it takes minutes to absorb). Leave the shredded wick on the skin and tape it down with a piece of clear tape about 4 inches long (this increases the time you have to work). Quickly wash your fingers.

4.Place your skin tissue specimen on one plate and the sugar specimen bottle on the other plate.

5.Probe for resonance every 5 seconds. As soon as you hear resonance, implying that the skin has absorbed the sugar solution (which may take a full minute), replace the skin specimen with one of liver and listen for resonance again. There should be none, yet.

6.Alternate between the skin and liver. Soon the skin will be clear and the liver will resonate. Also check the pancreas and muscles to see how quickly sugar arrives there.

7.Check white blood cells and kidneys. It should not appear here (unless it is polluted with a toxin).

8.After five to ten minutes the sugar will be gone from all of these tissues and your experiment is ended. Wash your arm with plain water.
 

Notice that you have only a few minutes to get all your testing done after the skin has absorbed the test substances.

True Origins Of Viruses
Your body can eliminate any virus in a short time, such as hours or days. It can even keep up with a steady stream that is coming from tapeworm stages!

Let us apply these new insights to several diseases we are familiar with. Let us speculate what could really be happening.

Epstein Barre Virus (EBV) is a mysterious disease because in spite of building up antibodies, it attacks repeatedly. I only see EBV if the person also has Eurytrema (pancreatic fluke) in the pancreas. When the fluke is gone, I no longer find EBV in the white blood cells. This suggests that the virus comes from the fluke. As each fluke dies and is finally removed, the body's white blood cells can catch up with the viruses and you begin to feel better again, which can be as quick as one day. But reinfection with an EBV-carrying Eurytrema (plus a wood alcohol containing beverage to allow the fluke to go to the pancreas) can spark the next recurrence.

Shingles is a recurrence of chicken pox. I always find Ascaris in persons with shingles! Unfortunately, killing the Ascaris does not cure shingles. Herpes Zoster (the shingles/chicken pox virus) is known to hide in nerve cells. Perhaps 4scaris facilitates it's release, or simply suppresses the immune system in a way that allows it to suddenly multiply.

Polio was once a scourge. At that time, we can theorize that a new large parasite was making its appearance. Was a new animal association taking place in the early 1900's? Life was. indeed becoming more urban with horse manure on all streets. Owning a dog for a house pet was becoming an acceptable lifestyle. Could the tapeworms of these animals give us a tapeworm stage that hosts polio virus? Many polio sufferers also had migraines. These are caused by Strongyloides, a horse threadworm. Does Strongyloides host polio virus?

The HIV virus infects us during the time the intestinal fluke, Fasciolopsis buskii, is being hosted. Persons test negative to HIV shortly after the fluke and its stages are eliminated.

Coxsackie viruses give us some of our encephalitises. I never see Coxsackie viruses without the bacteria, Bacteroides fragilis, and I never see Bacteroides fragilis without Ascaris (a roundworm.) I conclude that one lives inside the other!

We may be deriving viruses from all the roundworms, flukes, tapeworms and bacteria that infect us! It would be a fascinating study, simply to examine each of these parasites singly, searching for their viruses with an electron microscope. They could also be searched for using immunological methods.

Fortunately, your health improvement does not need to wait on such studies. Your electronic technique can detect them in your body long before you are made ill by them. You don't need to know their hosts in order to stop hosting them yourself.

It is a time of great change for this planet as pollution spreads from pole to pole. The growth of industrial activity, mining, chemical manufacturing, the food "industry", and personal habits like smoking have spread new chemicals to every comer of the globe. The element polonium, which is radioactive and in tosmokebacco , is harmful to human lungs, but may not be harmful to a small lung parasite, like Pneumocystis carnii.

Benzene, which is a solvent and extremely harmful to humans, may not be harmful to fluke parasites living within us. Propyl alcohol facilitates the intestinal fluke but is toxic to us.

Parasites are doing abnormal things. Is this because of pollution?

The tables are gradually being turned against us in favor of our parasites and pathogens. Such large changes are called evolutionary. Is the human species doomed, or will some of us "adapt". Will some of us survive to pass on our "better" genes to a new population of cancerresistant, AIDS-resistant, Alzheimer's-resistant, etc.-resistant humans? How many of us will die trying?