- PNI (Psychoneuroimmunology) is a wonderful adjunct to these therapies and can be best learned from The Healer Inside You: using PNI mind-body science to help heal your body, which contains a detailed at-home therapy protocol based upon PNI (Psychoneuroimmunology) research.
by Dr Hulda Clark, from The Cure for HIV and AIDS pg.1-46 Copyright
The word “cure” in the title was chose, rather than “treatment,” because it is scientifically accurate.
When the cause of an illness has been found and, by removing it, the illness can be stopped or prevented, a true cure has been found. When the cause is not found but the symptoms can be removed, helpful as it is, you have only found a treatment.
New and more effective ways to kill the HIV virus, however important, are merely treatments. I confronted the inconsistencies within the “facts” as they are presented by regular clinical researchers. The inconsistencies are huge and glaring. They led to the paths of inquiry taken in this book. My research was a search for the causes of HIV and AIDS diseases. I searched for ways to remove their causes. Then I observed whether this would actually lead to relief from the diseases. I did not search merely for relief from the diseases as regular clinical research does.
Syncrometer technology, described in the Syncrometer Science Laboratory Manual, available from the same publisher, makes such searches for causes and cures possible. Hopefully, others will repeat my investigations and extend my findings.
..Does this mean you can cancel your appointment with your clinical doctor? No, it does not. Although you will not need antiviral drugs after you test Negative and stay Negative with this “natural” program, you may still need antibiotics and clinical support for your AIDS. AIDS is a different disorder. Keep clinical help by your side until you no longer need it. Dr Hulda Clark
(from The Cure for HIV and AIDS preface copyright)
A New Challenge
From Time Immemorial Healthy People Have Held Sick People Hostage.
The Witch Doctor, Medicine Man and Woman, Herbalist and modern Clinician are all alike in this respect. They wish to keep information surrounding illness and wellness to themselves and away from the layperson so that a profession of medicine can grow and become lucrative. The Herbalist did not tell which herbs could relieve colds or bring on a woman’s menstrual period (birth control) for fear that the people in need would get them for themselves and not need (nor pay) the Herbalist. The modern medical profession overlooks information on prevention; it tries to make self-help and simple treatments illegal. All for the same purpose: to build and aggrandize their profession. This seems inappropriate, especially where communicable or widespread illness is involved. This example is taken from a text on herbology:
This [bath] is a safe and sane procedure and will prove most beneficial to those who are obese and desire to reduce safely. In combination with the internal treatment with decoction of Fucus, this course is worth considerable to very stout people, and should not be sold too cheaply. It is a grave mistake to put this scientific treatment in the same class as the many advertised nostrums on the market. It is also a mistake to let your patient know what you are using. If any do make this mistake, he will lose his client who will straight away go to a drugstore for supplies.
Shook, Dr. Edward E., Advanced Treatise in Herbology, Trinity Center Press, 1978, p. 172.
I believe hostage holding of the sick is immoral, fundamentally unethical, and needs to be stopped.
Besides the moral issue, there is a practical issue. It would benefit society much more if the sick person were quickly rescued and helped back to productivity. A healthy society benefits each of us immensely: Likewise, an ill society injures us immensely, even when it is half a planet away. With this book, I hope to give away as many secrets as I can about the cause and the cure of low immunity, AIDS and the HIV virus, letting the truth come first and “professional concerns” come last.
The human species can no longer afford to make a business out of illness. Global travel reduces our planet to the size of our backyards. In order to keep our own backyards clean, the neighbors must keep theirs clean. So it is with keeping our bodies free of viruses and bacteria. We all must be free of them. The concept of health as a narrow professional concern is obsolete.
This book is intended as a gift to humanity. I make a plea to the public and private sector of the medical community not to suppress this information but to disperse it regardless of liability or embarrassment from the simplicity and newness of the cure, provided only that it meets your standard of truth. As skeptical as you may be, if you cannot review the data presented here with the care and understanding it deserves, you should abstain from criticism until you have studied it.
Awareness Is Not What We Need
Which of us has not crashed into a closed glass door at some time? We believed it was open. The doorknob, the doorframe was visible, but our belief was stronger. We laughed in surprise at our mistake. It was not too costly. The AIDS mistake is very, very costly.
I recently tested eight young Africans for the HIV virus. Six were well, pursuing their studies or business. Two had illness, yet I found all eight had HIV/AIDS disease. All had benzene accumulation. All were parasitized by the larval stages of Fasciolopsis buski. And all had accumulated a large quantity of heavy metals and azo dyes in their bodies. This had already destroyed a significant fraction of their immune power, although they could not feel it.
To date I have tested many more samples of African drinking water than I had five years ago, both by Syncrometer and by analytical laboratories. They were Positive for benzene as before. What does this mean for us?
If scientists, doctors, governors continue to believe this is irrelevant, that traces of benzene in our food and beverages could not matter, nor traces of heavy metals and azo dyes, then we will continue to crash through the door of disaster.
Following these authoritative professionals come the activists and lay people who believe in them. It is a cascade of disasters with great social implications.
In the United States, traces of benzene pollute bottled water, bottled beverages, water that is chlorinated with liquid bleach that is intended for laundry use, our produce (via pesticide), our breads via baking grease (actually petroleum grease), and in general via solvent extracted flavors and colors. Traces of heavy metals and dyes pollute all sprayed produce and water that has laundry bleach added to it. Our path runs parallel to the African path.
Will the United States follow the African lead to annihilation? The trend will eventually become irreversible. It is unthinkable. Yet, six out of the eight Africans I tested, believe they are being spared. Most Americans believe they are being spared.
“Positively Aware” is a journal for HIV Positive persons. I recommend it for anyone who feels safe from this disease. Some recent topics were: Lost Youth, One in 62 Young Injectors, The Joys of Safer Sex, and HIV Drug Companies Sue South African Government. The journal is full of drug ads.
These drugs kill the HIV viruses coursing in the blood. They do not kill the source of the viruses, a common human parasite that has taken on a new life cycle. The Syncrometer easily spots the parasites in the genital organs, in the thymus and bone marrow. Eventually even the space under the skin becomes packed with larval stages. The Syncrometer “sees” them as easily as an infrared camera picks up a warm body. Superior technology can make it easy, but very difficult if belief interferes with rational thinking and declines its use.
I could cry on every page when I read “Positively Aware”. It is appropriate to sympathize and to cry. The tragedy is not just in the loss of human beings; it is in the journal itself, the very title. Nobody who writes it or reads it has an iota of real awareness, despite its assertive title. Even the editors of the magazine die of AIDS!
Their subscribers, and all affected people, need true awareness. That starts with a willingness to study new data, such as presented here, and which can lead to an understanding of the causes of HIV and AIDS diseases.
In this way, a similar path has been chosen for AIDS as for cancer research. It does not hold promise. The science of biology holds much more promise. Shouldn’t we sit up and pay attention to who is choosing the research path? The members of the AIDS community are exceptionally well informed. They are capable of understanding the research choices we could make, if only they were allowed.
___________________________________________________________________________________________
The Beginning: A New Concept
It is popularly believed that the HIV virus causes AIDS. But that is not true. My electronic studies prove otherwise. An unusual kind of parasitism brings the virus: a parasitism that is conditioned by the same environmental pollutants that cause AIDS. If ordinary biologists, like myself and hundreds of others, were allowed-in fact encouraged-to do the research in this disease they would have had its mysteries solved in just a few years. That would have brought its victims a true cure. It would also be shedding light on what is happening to the biosphere, which brings us new diseases such as this.
By allowing only high-tech “medical” research to be done, and excluding the rich diversity of biological research, the educational advantage of our nation’s biologists goes unused.
HIV is a virus.
AIDS is a condition.
Sometimes they occur together.
Sometimes they occur separately.
HIV stands for Human Immunodeficiency Virus.
AIDS stands for Acquired Immune Deficiency Syndrome
The HIV Virus
This is the source of the HIV virus
See Fig. 1 Human intestinal fluke (Fasciolopsis buski) (pg. 15. The Cure for HIV/AIDS)
This parasite typically lives in the intestine where it might do little harm, causing only colitis, Crohn’s disease, irritable bowel syndrome, or perhaps nothing at all. But if it invades a different organ, like the liver, uterus, kidneys, or thymus, it does a great deal of harm. If it establishes itself in the thymus it causes HIV/AIDS! It only establishes itself in the thymus in some people. These people have benzene in their bodies. All HIV patients (100%) have both benzene and a larval stage of the intestinal fluke in their thymuses. The solvent benzene is responsible for letting the fluke establish itself in the thymus. In order to get HIV, you must have both the parasite and benzene in your body.
The HIV virus belongs to this fluke.
See Fig. 2 Human intestinal fluke, typical size (pg.16 Cure for HIV/AIDS)
Parasites float when expelled from bowel. “Black hairy legs” are strings of eggs.
See Fig. 3 Five flukes in various stages of decay (pg.16 Cure for HIV/AIDS)
Many of us have this fluke parasite in our intestines. Humans are the natural host for this parasite. But they are seldom preserved well enough for you to identify in the toilet bowl. Later, when you have learned how to kill them in the intestinal tract in a way that keeps them better preserved, you will have a chance to see and recognize them (see page 166).
When this fluke is killed, together with its eggs and larval stages, the HIV virus disappears from the human body in 24 hours. Surprisingly, even latent viruses that are stuck in our (human) chromosomes, right beside our genes disappear. From this it can be concluded that the virus belongs to the parasite. The virus must be replenished by the fluke to persist.
IT IS NOT DIFFICULT to kill this parasite and all its stages.
In fact, the intestinal fluke and all its eggs and stages can be killed with an herbal recipe in six days, or less when electricity and homeography are used, too. These are explained further in the chapter Killing Parasites. The time, of course, depends on how many flukes and fluke stages you have. Read the early case histories, where only herbs were used, to follow the fate of the HIV virus. Compare them to the later case histories when electricity and homeography were added.
AIDS IS A CONDITION
AIDS reflects the condition of your white blood cells. We write them as WBCs. They are your immune system. There are a variety of them. The phagocytes are expected to eat bacteria, dead refuse and toxins. There are two kinds of phagocytes, the neutrophils and the macrophages. Other white blood cells are expected to destroy viruses. They are your lymphocytes, particularly CD4 and CD8 cells. Your WBCs are expected to make some powerful big-parasite killers: benzoquinone (“BQ”), rhodizonic acid (“RZ”), glyoxal, glyoxylic acid, and hydroxybutyric acid as well as others not yet discovered. We will discuss these later. But none of this is happening. There is very serious damage to all these immune functions.
Why?
If you have AIDS, your phagocytes have stopped eating anything, no bacteria, no refuse, no toxins. And the lymphocytes are filled to capacity with HIV viruses but are not able to kill them. In fact, they are full of flu viruses, SV 40 viruses and fungus too, but cannot kill anything. SV 40 stands for Simian Virus Forty. The chief fungus is Potato Ring Rot. And these problems are only the tip of the iceberg.
All this damage does not come from a single virus or toxin. The damage is vast and complex. But a new technology I call Syncrometer® science has made it possible to analyze the different parts of these two diseases, HIV and AIDS, and find their true causes.
The phagocytes have stopped eating anything because of four toxins – but only four.
The lymphocytes cannot kill viruses (any viruses) because they are full of mercury and thallium, not other metals.
The CD4 lymphocytes themselves get killed by a dye – a single one. The CD8 lymphocytes get multiplied as if they had cancer – again by a single dye. It is the same dye seen in cancer.
At first this immune damage happens at only a few organs but more and more follow this fate until every organ I study, dozens, show the same terrible acquired immune deficiency. When these deficiencies reach the thymus, the whole process is
The Thymus Gland And AIDS
The “T” in T-cells comes from the word thymus.
The thymus is located under the top of your breastbone. It is just below the thyroid gland.
To find these glands:
- Look in the mirror and turn your head from side to side.
- Notice a V-shape is formed at the front of your neck as you do this. Put your finger in the hollow at the bottom of this V. Your thyroid gland is on both sides of this V.
- Move downward from this hollow about 11/2 inches to a raised flat area shaped like a baseball plate. This is the top of your breastbone (sternum). Your thymus is under this, stretching down and up, depending on its size.
The thymus is the home for your T-cells. They were “taught” there what to attack, whom to help and which cells to kill. But something goes wrong here. The T-cells that are sent out “into the world”, namely your body, to protect you have garbled instructions and many defects.
An HIV victim also has fewer white blood cells, about 3500 instead of 5000. This develops gradually. Maybe not enough are being made in the bone marrow. Maybe something is killing them. Maybe both. The true cause of this is not yet known to clinical science. But the Syncrometer (see page 29) finds the same common toxin to be at fault, benzene.
See Fig. 4 Drawing of thymus gland (pg.16 Cure for HIV/AIDS)
The lymphocyte percentage for an AIDS sufferer is a little higher than normal; about 30% instead of 20%. A higher percentage of lymphocytes is the hallmark of any viral disease.
We normally have at least 5000 white blood cells in a cubic mm. (a very small dot) of blood. They are all made in the bone marrow. About 70% turn into neutrophils, which can phagocytize (eat). Another 10% turn into macrophages, huge cells that eat anything and shy away from nothing. They are the piranhas of our defensive WBC fleet. The remaining 20%, about 1000, grow up to be lymphocytes, our virus eaters. Nearly all of these, about 900, are sent to be “trained” for this in the thymus, and are called T-cells. The others are trained “at home” in the bone marrow, and are called B cells. Of the 900 T-cells, there should be about twice as many T-helpers (T4′s) as T-suppressors (T8′s), about 600 T4′s to 300 T8′s. They are also called CD4s and CD8s. Three names for each!
But now there are about equal numbers of helpers and suppressors, about 500 of each. Fewer and fewer helpers and more and more suppressors is a flag signaling HIV/AIDS disease. What could be happening to the thymus and the bone marrow to give such a picture?
Two things are happening. Not enough white blood cells are being made. And something is causing the T-helpers in the thymus to die an early death. Why? The bone marrow has a killer chemical on the loose, just where white blood cells are being born. And the thymus is being invaded by the intestinal fluke. The thymus is a small gland and the intestinal fluke is a large parasite! The thymus has a lot of work to do (like a taxi-dispatching station for white blood cells) and the flukes are eating its food and leaving their wastes in it. It is like having a bus full of people inside the tiny waiting room of the taxi station.
The same thing will soon happen to the bone marrow; a special class of dyes, called azo dyes, will flood it and the intestinal fluke stages will invade here, too.
The fluke will bring its own “personal” bacteria, Bacillus cereus, to the thymus. These bacteria make a special toxin called tyramine. Tyramine will make the thymus allergic! Allergic to a common food substance that arrives every day. Allergies consume immune power of the special kind called complement C3. Now the thymus, already burdened by benzene and the intestinal fluke, must share its immune power with yet another consumer. The more that is eaten of this food the slimmer the immune power becomes. Soon other parasites cannot be excluded. Paragonimus arrives. Eurytrema arrives bringing the SV 40 virus. All these events started with the Fasciolopsis fluke. And as you read the case histories a fascinating story is revealed.
Again, in each case, the real culprit is benzene.
Benzene
Benzene is a solvent. It is an extremely toxic solvent. We would not expect to find benzene anywhere in our environment. It is even monitored in gasoline. It is prohibited in dry cleaning fluids and rubber cement. How could it be present in your body?
Benzene is the main cause of AIDS
What is a solvent? A solvent is a substance that can dissolve grease. There are many solvents used in industries but none dissolves grease as fast as benzene.
The living body is made of greases! Fats and oils make up the brain and spinal cord, all our nerves and the protective covering of every living cell. Benzene can dissolve them!
Different toxins accumulate in different organs. This is called organotropism. As an example, if you drink a beverage polluted with wood alcohol, which is another solvent, it goes to your pancreas first. This organ makes your insulin and regulates your blood sugar. People with “low blood sugar” or chronic fatigue actually do have wood alcohol in their pancreas. Did they really drink polluted beverages? I find wood alcohol is a pollutant in carbonated beverages, artificial sweetener and many other foods. At first your body can detoxify it; this is when your body is young and strong like a child’s. But as you keep drinking the wood alcohol, the pancreas wears out, the wood alcohol begins to pile up there and do a lot of harm. It weakens the pancreas so much that any parasite can live there. The immunity of the pancreas is being lowered. Bacteria, viruses, fungi, metal dissolved from tooth fillings, chemicals from the air you breathe and food you eat can now find a home in your pancreas. Is it any wonder that this leads to diabetes? Wood alcohol also accumulates in the eyes. Sometimes they burn and itch. Now the eyes let parasites in to multiply, like Toxoplasma from cats. The eyes also let in toxins from food or your environment and we call it allergies. The real culprit in this case is wood alcohol! It accumulates in the pancreas and eyes.
Benzene accumulates in the thymus!
If you eat the tiniest bit of benzene accidentally, like eating a cracker while you are pumping gasoline into your car, it goes directly to your thymus (the cracker can absorb benzene containing gasoline fumes). If you rub the tiniest bit of benzene into your skin in the form of skin lotion containing petroleum products, it is found in the thymus a half-minute later! You can easily see this with a Syncrometer. And in another half-minute it is in the bone marrow. Of course, the white blood cell phagocytes that are in your thymus immediately begin to eat it up and get it out of the thymus. But something strange happens to phagocytes that have eaten benzene. They stop. They can eat no more – a rather sensible result! Nor can they eat anything else that they would normally devour and kill.
Just as wood alcohol accumulates in the pancreas and eyes, benzene accumulates in the thymus and bone marrow.
Without being able to phagocytize in the thymus and bone marrow everything else is soon allowed to land there. The mercury from metal tooth fillings, the copper from your copper water pipes, the silicone from your toothpaste, the dyes from your candy and jello can all be found in your thymus after benzene damage has been done. It is as if the front and backdoors to your house have been opened, letting in all comers.
Squatters Arrive
Soon the thymus is full of bits of your toothpaste, your hand lotion, your hair spray, your processed food, and your drinking water. Each of these has traces of azo dyes, heavy metals and myriads of other chemicals in them. Before the benzene damage, these loitering chemicals would have been phagocytized (eaten up) and escorted to the liver, to the kidney, and out of your body with the urine. Now they are left behind in the thymus and bone marrow and remain there, accumulating to higher and higher levels. Benzene keeps coming. The total WBC count (which includes your T-cells) falls lower and lower. Three special “squatters” arrive, also to be trapped in the helpless thymus: asbestos, metals and PCBs. I will discuss these soon. The thymus can’t keep them out. It is helpless because benzene has knocked out its phagocytizing capability. This means that the white blood cells belonging to the thymus cannot eat its enemies. From metals to E. coli germs, they would normally all have been eaten. Then they could not harm you. They would be taken away and dumped into your bladder. Here is a drawing, copied from an electron microscope picture of a macrophage (one kind of phagocyte) reaching out for E. coli bacteria. Long thin pseudopods (arms) would go out hunting for your body’s enemies-its breakfast. Now it must stop.
When you watch one of these phagocytes in action (this is called Live Blood Analysis) you can see that there is no action; they can barely move.
Benzene is not the only toxin that destroys phagocytizing ability. There are three more but only three! This seems fortunate in view of the hundreds of thousands of toxic things in our environment. They are asbestos, magnetic metals called lanthanides and PCBs.
Slowly, these three toxins accumulate along with benzene, each adding its own specific damage to phagocytosis.
Benzene is most important, though, because it harms the bone marrow, too, where baby white blood cells are being born. There will now be fewer phagocytes and less T-cells created. Their numbers go down at the same time as the remainder loses their phagocytizing ability.
Fig. 5 Phagocytosis brings in E. coli for breakfast (pg.24 Cure for HIV/AIDS)
Pathogens Attack
Meanwhile, the bacteria and viruses, which are hidden in our bodies, have been quietly waiting. Waiting for their chance to come out of hiding. Waiting for their chance to grow and multiply, as all living things must do to survive. When the phagocytes are muzzled and the WBC level falls low enough, they seize their opportunity. Look at the long list of pathogens (bacteria and viruses), which have come out of hiding in many of the case histories. Your body is a huge warehouse of pathogens and parasites. You have accumulated them in a lifetime. Chicken pox, mumps, measles, strep, flu, colds! Even TB, EBV, CMV, Treponema (syphilis), Mycoplasma, Toxoplasma, and the fungus Pneumocystis. Even Herpes, Candida, and Baker’s yeast. Even cMyc, RAS and SV 40 implicating oncoviruses.
Oncoviruses are tumor-causing viruses that have joined your chromosome DNA as if they belonged there. This lets them be multiplied by you. But only if a trigger is present.
- cMyc (avian myelocytomatosis virus) actually comes from the common blood fluke, Schistosoma, but it spreads to us, the host.
- RAS (murine sarcoma virus) comes from plain bread yeast that we eat in live form if bread is under baked.
- And SV 40 (simian virus) comes from Eurytrema, the pancreatic fluke.
Each one of these pathogens once entered and is still in your body somewhere! Nothing ever disappears completely. It just hides and waits. It is carefully bottled up. Some pathogens me hiding inside specially made capsules. They won’t come out of their capsules until they know they will be safe from your phagocytes and T-cells. Some are in a latent form or dormant state in which they patiently wait for your T-cell count to go down and phagocytes to be muzzled. Then they emerge. Some come from hiding in tooth crevices, like clostridium bacteria. These give us mouth odor. Clostridium makes dreadful odors. Some come from hiding in the nerve centers, like Herpes and Shingles. That is why we get genital warts and painful blisters. Some come from the digestive tract, like Salmonella and Shigella bacteria. They give us bloating and gas. Some come from the genital organs, like Treponema and Neisseria (gonorrhea). Some come from the lung, like Pneumocystis carinii. Even fungus and yeast can grow in humans as if we were bread or fruit. Now they come out and flourish, too, producing their deadly mycotoxins, like zearalenone.
We are accustomed to thinking that we “pick up” our infections. Certainly, we do keep picking up new strains. But we already have in us all the bacteria and viruses that could make us very ill if our immunity drops. They are not making us sick now because our immune system keeps eating them as fast as they might emerge. Most of them did not even make us sick when we originally picked them up because they were few in number and our immune system was strong at that time, too.
Now that the T-cell count is gradually going down and the phagocytes have been disarmed, your Pandora’s box of pathogens is opening, letting out one after another, until the body is seething with infectious organisms. Is it any wonder that you are getting sick?
Of course our white blood cells must do more than just eat, or phagocytize our enemies. They must kill them, too, and then spit them out or hand them on to other white blood cells to take to the bladder. We will see what interferes with this part of our protection later.
Yet, the human body is surprisingly tough and strong. It will put up a good fight. It may take 10 years before it begins to lose the battle. Then it is called AIDS, Acquired Immune Deficiency Syndrome, acquired from polluting the thymus and bone marrow with hundreds of bits of garbage without having a way to remove them. The body’s garbage disposal utility is gone.
The Garbage Dump
This garbage was thought to be “progress.” We are led to believe that “new, improved” foods and potions of any kind are “better”. When we see this label on a package we automatically reach for it. It may indeed, be doing a “new, improved” job on the dishes because cobalt is added to make spots invisible but cobalt, a toxic metal, is doing a “new, more toxic” job on your body. “New, improved” taste in your coffees and herb teas are due to adding flavor extracts to them, which also adds the solvents used in extracting! “New, improved” taste in cereals is due to added flavors, which are extracts, again bringing solvents to these foods.
The less that is done to a food, the less chance there is to pollute it. But, of course, such matters should not be left to chance. Processed foods should be tested before they arrive in the grocery store, at least for the five immune-lowering toxins they might have. This was never necessary before. We could count on the good common sense of bakers, cooks, canners, and manufacturers. But all these professions have become much more complex. Bakers don’t know what is in their ready-mixes, cooks don’t know what is in their ingredients, and manufacturers don’t know what their extraction solvents are. All these details are considered off limits to anyone inquiring (it is after all, mere “housekeeping”) and even beneath considcration of management! It is left to the technician. Technicians must keep the processing machinery working. They are “given” the solvents, chemicals and cleaners that “must” be used to keep it all working. So, choices important to our health are made by machinery manufacturers; not doctors, researchers or even owners of companies. We must protect ourselves!
Simpler is better
Tests exist for benzene, PCBs, lanthanides, heavy metals, asbestos, and azo dyes. The consumer no longer needs to stand by helplessly wondering if the water or some food is making the family sick. These tests only need to be correctly chosen and applied. This field of endeavor is very much needed now.
Not only food, but also body products, our artificial teeth, and our household products have become polluted with these same five immunity-destroyers.
Which Came First?
As we review the scene of the HIV virus growing and thriving in the presence of benzene we can’t help wondering, which came first? The virus or the toxin? I do not really know, although I made a case for benzene coming first, damaging the thymus by destroying its white blood cells’ phagocytizing ability. This then allowed the fluke eggs and stages to settle there, growing their own virus, specifically the HIV virus. The virus, in turn, infects us, but again, only when benzene is present. Benzene affects the enzyme that permits viruses to join our chromosomes. We will see the details later. Yet an equal case can be made for the parasite coming first.
We are all parasitized. This is the case for all animals. Being larger than most we can even host more than other animals. Having less instinct than others we cannot get rid of our parasites regularly as others do. In our belief that we are civilized, advanced, and even superior to our animal neighbors, we have handicapped ourselves. When we learn to purge ourselves as the animals (and primitive peoples) do, we see large flukes about the size of a nickel, small flukes the size of lentils, and sometimes Ascaris worms, like threads, the same as are vomited up by our cats and dogs. They are in our bowel contents.
We must learn to recognize them again. And we will, in the next chapter. What we cannot recognize are the larval stages, the microscopically small forms that do not look like the adult at all and that have landed in our organs, not the bowel contents. For that we need the Syncrometer device. When we see how many larval stages are thriving in us we can easily understand how parasites might reach the thymus first.
Regardless of which came first, it is the coincidence of Fasciolopsis larval stages and benzene that results in the HIV virus population explosion. The Syncrometer will let us see it happen.
Co-Parasites And Co-Viruses
By the time we are adults in our twenties, we are already quite parasitized. We are merely not sick yet. The commonest fluke parasites are Fasciolopsis buski, Fasciola hepatica, Paragonimus Westermanii, Eurytrema pancreaticum and Clonorchis sinensis. The commonest roundworms are Ascaris lumbricoides, Ascaris megalocephala and Strongyloides varieties.
Paragonimus and Eurytrema team up with Fasciolopsis in HIV/AIDS.
Eurytrema, Clonorchis and Strongyloides team up with Fasciolopsis in cancer. Eurytrema contributes the virus SV 40 in both cancer and HIV/AIDS. That is why cancer and HIV/AIDS have much in common. Teamwork is not necessarily intentional. Two parasites or viruses can share a space, our bodies, the way a cat and dog can share their owner’s home.
Together, a trio of parasites can bring symptoms quite different from either one alone. And larval stages bring symptoms quite different from adults. All this leads to confusion of the doctors, parasitologists and researchers who are accustomed to the classical symptoms they were taught to expect.
But a new technology allows us to see all these events as they happen.
Let us spy on the white blood cells with a Syncrometer see how the Paragonimus-Fasciolopsis partnership works.
Watching The Thymus
Technology has become so advanced in the fields of communication, TV, optics, and imaging that any application of these new fields to biology is likely to bring leaps of progress in our understanding.
The simple application of a voltmeter to the human body brought us the EKG and the EEG from which a great deal of knowledge was gained.
Magnetic resonance and CT (computerized tomography, pronounced cat) scanning techniques brought us the ability to “look inside” our bodies and “see” density differences in our (issues.
By applying a one-transistor amplifier to our bodies and using a pair of open-plate capacitors in the circuit, we have created a radio receiver-like station, which includes the body. Now we can “listen in” to the frequency patterns that are “in Line” (on the capacitors) with the body’s patterns.
This device is called a Syncrometer.
Instructions for building and using one are given in the Svncrometer© Science Laboratory Manual by this author.
In this way we can detect and identify things at specific locations in the body, even in the chromosomes. With this device we can watch the thymus or any other organ, as the parade of parasites and toxins come and go. In previous books I tracked the benzene to its outside sources: toothpaste, ice cream, store bought bread, bottled water. Since then I have also tracked it to Paragonimus flukes, a totally inside source. Let us “tune in.”
We “hear” the white cells spitting bleach at the Paragonimus family-its eggs and stages. It is regular bleach, hypochlorite, one of our immune system’s weapons. They are doing this in different organs where this parasite resides. In 20 minutes nothing is left of the Paragonimus family. We can no longer “pick up” on their frequency pattern. Are they merely stunned or paralyzed? We check every hour. Suddenly, at all these organs a fungus grows in exactly the same place. Pneumocystis is there now, not Paragonimus at all!
The white blood cells seem furious. They attack again with a different weapon. But still, another new fungus takes its place, this time common Potato Ring Rot. We eat this every day in our under-baked potatoes. It can grow in us, too. But our WBCs can destroy and eat it. Soon all fungus is gone, the deck is cleared, everything is clean again and the white blood cells go searching for new enemies. Fasciolopsis and all the other parasites are attacked the same way. Only the fungus is different for each parasite variety. See fig. 6 Potato Ring Rot mold hidden in potatoes (pg.30 Cure for HIV/AIDS). We cannot avoid getting these parasites in ourselves because we eat them constantly. We eat all the spores, too, that provide the fungi that will consume any dead parasites.
Let us watch now what is happening in an HIV/AIDS patient. The white blood cells are spitting bleach at a Paragonimus lair we have singled out with our Syncrometer. It takes longer but soon the whole family is gone. A few hours later, the same location is occupied by a Pneumocystis patch, as before, then by Potato Ring Rot. The white blood cells are devouring this now but it takes too long. The fungus is already inside the phagocytes but yet it isn’t dead. This is puzzling. The fungus starts to make its mycotoxin, zearalenone. And minutes later, the zearalenone is being “detoxified” into benzene! This is the same benzene that is so deadly! It lingers, too, much too long. It will soon stop phagocytosis there, as a small “pond” of benzene develops. It is creating a huge hazard, like a lighted match near a gasoline can. Benzene happens to be the critical solvent that triggers the HIV virus. This virus is merely ,a latent virus in a different parasite some distance away and not as common as Paragonimus. It is Fasciolopsis. If the benzene lingers long enough and spreads far enough to reach the Fasciolopsis, its HIV virus will be triggered out of its sleep (latency). HIV will be activated. The Syncrometer can now “hear” the virus, in louder and louder resonance. It begins to multiply the way Herpes does when we supply its special triggers. Now HIV can spread to our bodies.
We can see that many HIV viruses are produced and escape into us. Some enter our chromosomes because benzene can trigger them in as well as out of our genome, using an “integrase” enzyme. The benzene caused the sudden appearance of this enzyme.
But we are huge animals, compared to these tiny parasites. All we need to do is kill most of them when they are still quite manageable. Instead, in our ignorance, we are eating and absorbing the very trigger for the virus. And we are too arrogant to admit parasitism, or to use herbs to fight them. Anyone can learn to use the Syncrometer and watch this scene going on in our own and others’ bodies.
Endogenous Benzene
Endogenous means self produced or internally produced. No biologist or biochemist could suspect or even believe that
benzene could be produced by a living organism, neither plant nor animal.
Yet the Syncrometer clearly reveals benzene being formed wherever zearalenone is present. Zearalenone is present wherever Potato Ring Rot is growing. Potato Ring Rot is a fungus that grows wherever a Paragonimus parasite has been killed. Paragonimus is plentiful alongside Fasciolopsis buski, Fasciola hepatica and others. It is more plentiful in HIV victims for reasons not understood. But while it is alive it does not grow Potato Ring Rot, so the mycotoxin zearalenone is not produced, nor benzene. But dare to kill Paragonimus and within hours the deadly fungal growth takes over the carcass. This fungus makes the estrogenic toxin zearalenone, and this leads to benzene production on the spot.
Would it be better not to kill Paragonimus parasites? The body’s instinct is to kill everything foreign, everything that attacks you, competes with you, or takes up your space. It is a precious instinct. Yet, could benzene production be nature’s intent? Or has Mother Nature gone awry in this instance? I believe we were meant to digest old dead refuse, so that fungus could never take over. But for HIV victims this kind of digestion is lacking.
We make lots of digestive juices in the stomach and in the pancreas. We are regularly flooded with it at mealtime. The Syncrometer® detects hydrochloric acid (HCl), pepsin, trypsin, lipase, RNAse, DNAase and even asparaginase sweeping into every tissue in children. But in middle age there is much less. The tissues, even the stomach itself, go without HCl and digestive juices for brief periods of time. Now killing Paragonimus leads to benzene production whereas in childhood it didn’t. Of course the body can detoxify these traces of benzene at first. And some is eaten by white blood cells. But this stops their phagocytizing ability. Although it is a wise response by the white cells the entire burden is then shifted to detoxification instead of removal. Benzene is detoxified first into phenol. Benzene released in and around the thymus from killed paragonimuses gets changed to phenol. But phenol, although not a solvent, is a powerful tissue destroyer; now the thymus will begin to shred and lose bits of itself into the circulation. Fig. 7 Benzene is detoxified to phenol (pg.33 Cure for HIV/AIDS)
Still, the body has been dispatching its parasites and disposing of the remains, including benzene and phenol, for eons of time. It did not lead to AIDS. It only led to gradually declining body functioning and overall aging.
But in this century it leads to AIDS. The total amount of benzene to be removed or detoxified has been doubled or worse in this century. We have dumped it on our food (pesticide), even mixed it in our food (baking grease, flavors and colors) in wholesale amounts. We have fumed it into our air (exhaust, colognes, cigarette smoke). Every liter (quart) of air in an office or even outside in a meadow has its benzene, detectable by regular chemical methods. This means a few parts per trillion.
With this huge increase in benzene how can a fragile, phagocytizing white blood cell escape destruction? How can a nation’s immunity escape gradual destruction? How can global immunity escape destruction? We cannot rest; a way must be found.
The body has always managed to get rid of its endogenous (internal) benzene and allowed us a lifespan of 70 to 80 years. But adding exogenous (external) benzene has given us AIDS, driving our lifespan down to about 40 years. We must fight back on both fronts. We can clean up our food and environment, the exogenous sources. We can kill our personal parasites regularly, our endogenous sources, so they cannot mature to the point of laying eggs and outrunning the body’s ability to kill them.
Eurytrema Brings SV 40 Virus
The pancreatic fluke inhabits the pancreas of cattle. All milk and beef products have some stages of it. But when we host this parasite it is not restricted to the pancreas. It can thrive wherever there are tissues with low immunity. This is the thymus and bone marrow for an HIV/AIDS victim.
Spying on a Eurytrema lair we see it is constantly releasing the SV 40 virus but only if gallic acid is present. Gallic acid is the trigger for this virus. Gallic acid comes from a common food preservative, propyl gallate. It is also found naturally in certain foods. We will see how SV 40 aids and abets the HIV virus in some mysterious way. Because they interact, I call these viruses “co-viruses” and the parasites “co-parasites.” Not all the details are clear but some are very obvious to anyone using a Syncrometer.
Parasites Plus Benzene
More Immune Defects
Azo dyes, in our foods and body products, act on our lymphocytes. Outright killing of CD4 cells by Fast Garnet dye and overgrowth of CD8 cells by Fast Green dye are two effects. Other dyes do more damage and need study.
Certain food substances called allergens or antigens specifically target the thymus after Fasciolopsis arrives there. One is apiol. Another one is gallic acid. And all along, the harsh chemical, phenol, has been damaging the thymus simply because it is the detoxification product of benzene which accumulates there.
These allergens use up all the complement C3 in the thymus. C3 is necessary for “killer” action by white blood cells. So yet another immune defect is occurring.
We will also see that many of our strongest immune weapons are not being made.
- Benzoquinone and rhodizonic acid are overwhelmed by our two main Ascaris varieties that would normally be killed by them.
- Glyoxal is overwhelmed. by Eurytrema, the pancreatic fluke. Glyoxylic acid is overwhelmed by Strongyloides
- L-G and L -A are overwhelmed by heavy metals, both those naturally made in the body and those like mercury and thallium coming from dental amalgam.
- Betaglucan is overwhelmed by PCBs.
- Interleukin 12 is missing when holmium (a PCB cotoxin) is present.
- Interleukin 2 is missing when L-G is missing.
- Interferon is missing when RAS is present.
We will discuss these later.
But benzene starts it all. It increases parasitism. Parasites and viruses thrive in its presence leading to more immune damage.
In spite of all this, the body responds with the speed of an arrow, minutes, when the good things are supplied and the bad ones removed. Soon the body can be functioning normally again.
There are many more flukes that can parasitize us. There is Prosthoganimus, a fluke from chickens; Cryptocotyle, a fluke from sea gulls; Platynosomum, a cat liver fluke; Echinostorna, a fluke that rests itself on our neuro-muscular junctions causing ALS and fibromyalgia; Acanthocephala, (still quite mysterious); Echinoporyphium, cause of kidney disease, and several
blood flukes, the Schistosomes.
If we have a few of these, they don’t make us very sick. But when they have a population explosion, swarming in one of our organs, we get sick. Perhaps solvents cause such population explosions. Solvents could dissolve away the eggshells forcing them all to hatch. Hatch in your body! Normally, this would not happen. The eggs produced by the adult, thousands every day, are passed into the intestine to, exit with the bowel movement. But if they are forced to hatch before they exit, they swim away, into your body!
Even strange and rare parasites are becoming more common, no doubt due to new solvents that are entering and polluting our bodies.
Flukes
To understand HIV disease you should understand the basic facts about the human intestinal fluke. Its scientific name is Fasciolopsis buski. Fluke means “flat”, and flukes are one of the families of flatworms. It is as flat as a leaf. This lets it sandwich itself in between your tissues without your noticing it…without causing a disturbance or pain. The parasite is not unknown; it has been studied since at least 1925.3 This study was done in China. Since then it was often believed to exist only in China and tropical countries. Yet specimens for study in Parasitology classes come from the local abattoir, from pigs and cattle (even wild deer and moose)!
This parasite has stages that it must go through to keep reproducing. The first stage is the egg. The adult produces millions of eggs. They pass out of us with the bowel movement. The adult, though, stays tightly stuck to our intestine (or liver causing cancer, uterus causing endometriosis, thymus causing AIDS, or brain contributing to Alzheimer’s disease).
Most of us get little lesions in our intestines from time to time. These tiny sores allow the eggs, which are microscopic in size, to be pulled into the blood stream (other parasite eggs get into the blood this way, too).
Some of these eggs actually hatch in the intestine or in the blood. The microscopic hatchlings are called miracidia and are the second stage. They swim about with their little swimmer-hairs. And of course, the liver whose job it is to dispose of toxins and intruders will receive them and kill them as the blood arrives from the intestine. They have no chance to survive in healthy people.
Flukes And Solvents
But something special happens to people who have solvents in their bodies. The liver is unable to kill these tiny fluke stages. These baby stages are actually allowed to make their home in the liver and other tissues. It is as if the immune system has no power to kill them. The flukes begin to multiply in people with solvents in their bodies! The miracidia (hatchlings) start to make little balls inside themselves, called redia. But each redia (ball) is alive! It pops itself out of the miracidia and begins to reproduce itself. Forty redia can each make 40 more redia! And all of this out of one egg!
This parasite is laying eggs and producing millions of redia right in your body! These redia are swept along in your blood, landing in whatever tissue lets them in. Smokers’ lungs, breasts with benign lumps, prostate glands full of heavy metals, a thymus loaded with benzene are examples of tissues that give the redia their landing permits. Perhaps it is the changed electrical charge or magnetic force of these damaged organs that permits further development of the fluke stages. Perhaps it is merely low immune surveillance. Perhaps the dying cells of a damaged organ provide food for the baby stages. Only further scientific study will reveal the truth.
Multiplying continues at a hectic pace, generation after generation. Redia are nesting in numerous organs. Suddenly they change their shape. They sprout a tail and can swim again.
Now they are called cercaria.
The Latin names are rediae (plural) and redia (singular). I have used simplified spelling, “redia”, for both the singular and the plural, more like English usage.
Again, I am simplifying the Latin cercaria (singular) and cercariae (plural) to one case.
The cercaria only need to find a place to attach. After they glue themselves to your tissue, their tails disappear and they begin to grow a “cocoon”.
Now they are called metacercaria. Normally, this would happen on a leaf growing near a pond, so the metacercaria develop an extremely thick shell around themselves to withstand the winter. Does the presence of the solvent benzene in your body dissolve this tough shell? That would remove the last barrier to the fluke completing its entire life cycle anywhere in your body!
After the shell is gone, they grow into adult flukes in your tissue. NOT IN THE INTESTINE BUT IN YOUR THYMUS! IN YOUR BONE MARROW! IN YOUR SKIN! Now the cycle is complete. From egg to miracidia to redia to cercaria to metacercaria and then the adults! And all of them eating and sucking and devouring your vital body fluids.
But this is not normal for flukes. This is: See Fig. 16 Fasciolopsis’ normal life cycle (pg.38 Cure for HIV/AIDS)
As you can see, humans typically are the host for just the adult stage, and then only in the intestine. But can you imagine the havoc in your body if you did the snail’s job, too? Suppose the host, the human, has solvent in his or her body so that the millions of eggs start hatching before they can exit from the bowel. They simply swim in hordes into the blood stream. They may be searching for a snail but certainly a living tissue of yours will serve as well! To survive they must avoid being killed and eaten by your white blood cells. So a tissue where the white blood cells are inactivated by asbestos, thulium, PCBs, or benzene is the choice. They have found a home! In you!
Xylene and toluene accumulate in the brain so the fluke parasites choose the brain for their breeding place. Here they produce their redia and cercaria and eventually adults! Wood alcohol accumulates in the pancreas and eyes, making these organs the fluke breeding grounds. Isopropyl alcohol accumulates in the liver, making the liver the place where the stages develop to adults. And benzene accumulates in the thymus and bond marrow so that the intestinal fluke is raised up to adulthood in these small organs instead of the spacious intestine.
In this book you will learn how to kill it.
Many persons who have an adult fluke in the thymus feel a burning sensation or “tightness” over the breastbone. But some persons feel nothing at all. And some persons with “tightness” there do not have this parasite. So having a symptom here, while very suggestive of this fluke, does not prove you have it. However, it would be very wise to go on a parasite-killing program immediately, such, as I will describe to you later.
The HIV virus is brought into the body by an intestinal fluke stage inhabiting the benzene-damaged thymus.
All cases of HIV seen in my office since 1990 had benzene in their thymuses. Benzene had stopped phagocytosis there by the white blood cells. The thymus had PCBs as well as the azo dyes, Fast Garnet and Fast Green. It had heavy metals, including the magnetic ones and the metals in amalgam!
No case of HIV was seen without benzene in the thymus.
All cases of AIDS also had other flukes in their thymuses. Progression from early HIV/AIDS to advanced illness brought with it much more intense parasitism and more immune defects. There was very little BQ (benzoquinone), or RZ (rhodizonic acid), or G (glyoxal), or GA (glyoxylic acid) anywhere, and no L-G, L-A, interleukin 2, or interferon.
Weapons Of Mass Destruction
Early in the last century, before medical research had become a business and a monopoly, a young man graduated with a Ph.D. in chemistrv and biochemistrv. He was William F. Koch. His first postgraduate job was in a hospital where cancer patients were being treated, quite futile, then, as now. He put his chemistry to work, during free time, and found methyl guanidine in their urine, a most unlikely chemical, and in large quantities. This was more than surprising because it was the same chemical he had found in the dogs he worked with so recently for his Ph.D. degree. They had been deprived of their parathyroid glands. This coincidence kept him glued to cancer research for the rest of his life, using his own earnings to do it.
He went on to get an M.D. in order to pursue this lead. He felt that this chemical should have been oxidized by a healthy person. He was eventually led to a concept of disease in general, not just cancer, that involved missing oxidations by the body. Young persons, he postulated, had strong oxidation capability in their body chemistry. Sickly and older persons lacked something. This “something” was a very strong oxidizer. Other workers, starting with Otto Warburg in Germany, were studying a similar peculiarity: cancerous tumors did not consume oxygen, as they should.
He decided to try substituting other oxidizers; maybe the beleaguered organ could use them instead. He had chosen benzoquinone first and was instantly successful! Even though it was an industrial chemical, very powerful and of course toxic in any large amount, the body could use it. His theory was supported. He cured very many cancer cases with a single shot of 1 microgram of benzoquinone. The smallness of the quantity is astounding and important, just as it is for vitamins A, D, Bi2, hormones and ultra trace minerals. Larger doses are damaging.
He tried another oxidizer, rhodizonic acid, and was again successful. He tried them in combination and was even more successful. Then he tried “glyoxilide” (composition of this is not clear) and was so successful for numerous diseases, that he had his results independently verified, documented in a number of books, and used in a court trial. His books are in libraries.
He was shocked, as you and I would be, with such miraculous results. It was certainly worth pursuing this approach. He continued to search for the body’s own “natural” high-powered oxidizer. This would surely be the body’s “cannon” of force that could restore the body’s own ability to destroy its tumor growths and cure many of its other diseases. He never found it. At least he never thought so.
The Syncrometer, however, detects actual benzoquinone and rhodizonic acid as well as glyoxal and glyoxylic acid (perhaps his “glyoxilide”?), in every organ of a young person’s body! But in smaller amounts than he could detect, and it is lacking in diseased organs or an older person’s body. We have abbreviated them BQ, RZ, G, and GA. When a shot of BQ (1 microgram) or RZ is given, miracles happen to cancer patients. (See the book, The Cure For All Advanced Cancers, case histories #1, #6, and #7. All this urgently needs more research.)
BQ is, in fact, our natural high-powered oxidizer, a cannon of force, as are RZ and others. Dr. Koch would be more than gratified to know this. We owe him a huge debt. The Syncrometer® shows that these immune weapons can kill our large parasites, our flukes, our roundworms, including Ascaris of two kinds. Even when they are beyond attack by the WBCs! It is this kind of “natural immunity” that is missing in HIV/AIDS patients, besides the defects in phagocytes and lymphocytes and the lack of complement C3.
Yet, we do not need to procure BQ or RZ glyoxal or glyoxylic acid, nor take them. We can send an electronic message in the form of homeographic drops to your body to make them. The body does so promptly. It will overcome the Ascaris, kill flukes at the same time, and then keep on making these immune system weapons for you at any location that you choose.
We would, of course, choose to return BQ and RZ as well as G and GA to your thymus and the bone marrow first. Both organs can be re-armed with their natural cannons in a day. I will describe the details later. We will also use L-G to clear out heavy metals like mercury, thallium and all the others that come from amalgam. We will use L-A to clear out the “natural” heavy metals, such as oxidized selenium and germanium, chromium and nickel, copper, cobalt and vanadium. This will let the WBCs make interIeukin 2 again. Soon the AIDS is stopped and you are recovering.
Killing the parasites, removing benzene, and supplying immune weapons is a powerful three-pronged approach against HIV/AIDS.
Purge The Parasite, Cure HIV
When the benzene is gone but Fasciolopsis is still there, will HIV continue to appear? No! The virus simply vanishes, gone back to being latent. Benzene is the necessary trigger for HIV viruses to come out of this parasite and spread to our bodies. But, of course, we plan to kill Fasciolopsis anyway and not live in constant danger.
Even when the virus has become “ours” by slipping into our chromosomes, benzene is the necessary trigger that allows it to multiply and spread.
Fortunately, flukes are much easier to kill than roundworms like Ascaris or even certain bacteria. There are four ways to kill the intestinal fluke: an herbal way, electrical zapper way, the homeographic way, and simple starvation. Neither can do a perfect job by itself Yet a good job must be done, so it is best to use all four ways of killing them. The exact recipe and other techniques will be described in the next chapter. But don’t wait until you have all the supplies-start immediately with any method you obtain.
Look at the case histories. It is not unusual for someone to have a dozen or more parasites out of the 120 parasites I have samples of and can test for. You can assume that you, too, have a dozen different parasites. We are heavily parasitized beings! Our bodies are large enough to provide food and shelter for lots of these free loaders. If they were settled on the outside where
we could see them, like lice or ticks, we would rid ourselves in a flash. Nothing is more distasteful to the imagination than hordes of biting, chewing, crawling, sucking creatures on our flesh. But what about in our flesh? We cannot see inside ourselves, so we have mistakenly assumed that nothing is there.
To get well, you should do three things:
- Rid your body of the five immunity destroyers: benzene (this would also remove phenol), asbestos, metals, azo dyes, including Fast Garnet the CD4 killer, and Fast Green the CD8 elevator).
- Restore your immune weapons: BQ, RZ, G, GA, L-G, and L-A.
- Kill Fasciolopsis and other parasites, together with their stages.
(from The Cure for HIV and AIDS pg.1-46 copyright)