Alleged Cure For Cancer, Cancer Is A False Placenta Theory

[TreasureVibe]

The Cure for Cancer

ABSTRACT

The theory that malignant cancers are false-placentas (partial pregnancies) was first formulated by the Scottish embryologist John Beard in 1902. Beard found that substances secreted by the pancreas would inhibit the growth of cancers before they develop but are missing in the blood of cancer patients. These substances, the digestive enzymes trypsin (and the trypsin precursor chymotrypsin), reportedly “cure” (digest) 100% of fast-growing cancers when taken orally at an extremely high dosage. This author has found evidence that it may be possible to achieve the same cancer-digestive effect, with lower enzyme dosages, by enhancing trypsin's enzyme activity with certain supplements.

THEORY

John Beard was a brilliant biologist whose main research interest was pregnancy, and the placenta in particular. He made or confirmed several crucial observations that led to his theory of cancer. He observed under the microscope that the trophoblast cells that form the placenta looked like cancer cells. Beard then made an extraordinary observation: The placenta stops growing on day 56 of the human pregnancy - on the same day the fetus’s pancreas begins to function. He came to the conclusion that the fetus’s pancreas secreted something that stopped the growth of the placenta. He then surmised, and later proved, that the same substance stopped the growth of malignant cancer. He set out to determine what this pancreatic substance was.

Beard conducted experiments with the juices extracted from young animal pancreases. These juices were injected into cancer tumors and the tumors shrank in both animals and humans. Beard’s work was published in JAMA and he wrote a book on the enzyme therapy for cancer. One hundred years ago, physicians tried to duplicate Beard’s experimental results, but they failed, and the work was almost forgotten.

We now know that “delicate” enzymes can lose their effectiveness if not carefully extracted from young live stock. Even though trypsin was one of the first proteins whose molecular sturcture was deciphered by chemists in the 1960s, we are still not able to synthesize either trypsin or chymotrypsin. As pure trypsin must be extracted intact from young livestock, the cost of supplements with these enzymes is high. The cost at the dosage recommended by enzyme/cancer experts may exceed $2000 per month.

 

[Fractality]

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[Lore]

The Cure for Cancer

ABSTRACT

The theory that malignant cancers are false-placentas (partial pregnancies) was first formulated by the Scottish embryologist John Beard in 1902. Beard found that substances secreted by the pancreas would inhibit the growth of cancers before they develop but are missing in the blood of cancer patients. These substances, the digestive enzymes trypsin (and the trypsin precursor chymotrypsin), reportedly “cure” (digest) 100% of fast-growing cancers when taken orally at an extremely high dosage. This author has found evidence that it may be possible to achieve the same cancer-digestive effect, with lower enzyme dosages, by enhancing trypsin's enzyme activity with certain supplements.

THEORY

John Beard was a brilliant biologist whose main research interest was pregnancy, and the placenta in particular. He made or confirmed several crucial observations that led to his theory of cancer. He observed under the microscope that the trophoblast cells that form the placenta looked like cancer cells. Beard then made an extraordinary observation: The placenta stops growing on day 56 of the human pregnancy - on the same day the fetus’s pancreas begins to function. He came to the conclusion that the fetus’s pancreas secreted something that stopped the growth of the placenta. He then surmised, and later proved, that the same substance stopped the growth of malignant cancer. He set out to determine what this pancreatic substance was.

Beard conducted experiments with the juices extracted from young animal pancreases. These juices were injected into cancer tumors and the tumors shrank in both animals and humans. Beard’s work was published in JAMA and he wrote a book on the enzyme therapy for cancer. One hundred years ago, physicians tried to duplicate Beard’s experimental results, but they failed, and the work was almost forgotten.

We now know that “delicate” enzymes can lose their effectiveness if not carefully extracted from young live stock. Even though trypsin was one of the first proteins whose molecular sturcture was deciphered by chemists in the 1960s, we are still not able to synthesize either trypsin or chymotrypsin. As pure trypsin must be extracted intact from young livestock, the cost of supplements with these enzymes is high. The cost at the dosage recommended by enzyme/cancer experts may exceed $2000 per month.

Keep up the good work!!! and thank you!

 

[TreasureVibe]

An excerpt from a book published in 2017 by the controversial author Dr. William Donald Kelley. The book is called One Answer to Cancer:


"The Direct Cause of Cancer is The Changing of an Ectopic Germ Cell into an Ectopic Trophoblast Cell

The direct cause of cancer, according to our research, is the changing of an ectopic germ cell into an ectopic trophoblast cell. An excess of female sex hormones brings about this change. Both men and women have male and female sex hormones. When this delicate male-female sex hormone balance is upset, cancer may start.

Let me explain this a little further. In the human life cycle, the male sperm unites with the female egg. Now if this fertilized egg would grow directly into a new baby, we would have no cancer or cancer problems, but nature does not act so simply and directly, for if she did, the newly formed embryo (baby) would fall out of the uterus. Therefore, nature had to develop some way to attach the new embryo to the wall of the uterus and some way to nourish (feed) it.

After the sperm in the fallopian tube of the mother fertilizes the egg the fertilized egg gives rise to three basic kinds of cells:

1. Primitive germ cells
2. Normal body or somatic cells
3. Trophoblast cells

By the third day the fertilized egg has fallen into the uterus. During those three days and for many days thereafter, the trophoblast cells (cancer cells) are growing very rapidly and surround the other types of cells (primitive germ cells, and normal body or somatic cells).

The new baby will fall out of the uterus unless something happens fast, and happen it does. The trophoblast cells metastasize (as cancer does) to the wall of the uterus. Now the baby cannot fall out of the mother's uterus, but needs nourishment. The trophoblast cells (cancer cells) continue to grow rapidly and form the placenta. Now with a good food supply and no danger of falling out of the mother, the baby (embryo) can continue to grow, safe and sound, until birth.

The placental trophoblast tissue (cancer mass) continues to grow until about the seventh week when the baby's pancreas develops.

The baby's pancreatic enzyme production along with the mother's pancreatic enzyme production stops the growth of the placental trophoblastic tissue.

As the new embryo (baby) is being formed from the normal body or somatic cells, the primitive germ cells (pre-placenta cells) are multiplying. In a few days, when the embryo (baby) develops to the proper stage, the primitive germ cells stop multiplying and begin to migrate to the gonads (ovaries or testes).

There are about three billion of these primitive germ cells that fatigue and never have the vital force necessary to reach the gonads. This means that there are two germ cells for every area the size of a pinhead dispersed throughout your body. Any one of these germ cells is a potential cancer. That is why cancer can form in any part of the body. All that is needed to create cancer in our body is a deficiency of pancreatic enzymes, an imbalance of sex hormones and the embryonic destiny of a basic germ cell to form a placenta in preparation for the creation of a baby. The imbalance of sex hormones can take place at any time, but usually it occurs between 45 and 60 years of age.

When all is said and done, cancer is a normal growth of tissue (a placenta) due to the development of a basic germ cell in the wrong place (outside of the uterus). Sometimes this placenta also has a "baby" or begins a tumor inside of it much like a normal pregnancy - only it is in the wrong place. (When dissecting tumors Pathologists often find partially formed teeth, toenails and other types of tissue, such as lung tissue, within the tumors.)

Malignancy, therefore, is never normal (somatic) tissue gone into wild proliferation, but a normal primitive germ cell growing normally in the wrong place."


Book link: One Answer to Cancer

I was actually watching this video earlier today about a tv show in which they dissect a tumor from a woman, showing hair growth and teeth on the inside of the tumor:



The author also recommends PUFA in his book, which we know is poison, but to me that does not necessarily mean we should go full McCarthyism on him and disregard everything he has to say.
The author actually passed away in 2005, so the book was probably written before that, when research on PUFA was not as extensive as it is today. His conclusion that somatic tissue (normal body cells) never go into wild proliferation (growth) is also something that should be taken with a grain of salt ofcourse, for the sake of safety with too few data available currently.

Also basically, ''female sex hormones'' means estrogen, which corresponds with the study that @haidut posted here that cancer is caused by estrogen:

Estrogen As The Main Cause Of Cancer And Its Progression


The idea that pregnancy and cancer have alot in common, is also something mainstream researchers have picked up, as can be seen in the following 2009 study:

Cancer and Pregnancy: Parallels in Growth, Invasion, and Immune Modulation and Implications for Cancer Therapeutic Agents

 

[TreasureVibe]

TROPHOBLASTS AND THEIR RELATION TO CANCER

by Lawrence Wilson, MD

© October 2014, L.D. Wilson Consultants, Inc.



All information in this article is for educational purposes only. It is not for the diagnosis, treatment, prescription or cure of any disease or health condition.


An unusual human and mammalian cell type is possibly responsible for all cancer in the body. This is called the trophoblastic theory of cancer. To save time, I am going to explain this by excerpting a page or two from another book, Sauna Therapy, where the topic is addressed in more detail:


What is Cancer?

In 1902, Dr. John Beard published a paper in The Lancet on the trophoblastic theory of cancer (Beard, J., 1902). It is quite simple and has never been disproven. In fact, it recently received strong confirmation by scientists at the University of Michigan (Townsend Letter, #240, 2003). Dr. Beard showed that a normal tissue of the body, the trophoblast, exhibits characteristics identical to cancer. It is invasive, metastatic, forms new blood vessels (angiogenesis) and has the same specific markers and chemical composition as cancer cells.

The trophoblast is a totipotent or stem cell that grows around the developing fetus during the first eight to twelve weeks of pregnancy. The word trophoblast means 'nourishing the baby'. It burrows into the lining of the mother's uterus and supplies the fetus with blood until the placenta forms. It is essential for life.

The trophoblast normally disappears between 8 and 12 weeks of pregnancy. If it overgrows, the result is a very virulent form of cancer, choriocarcinoma. It usually kills both mother and fetus within a few weeks.

One may say, if the trophoblast only develops during pregnancy, how can it explain all other cancers? Dr. Beard found that the stem cells that form the trophoblast are present all over the body in small numbers. Given the right stimulus, they begin to grow. A key to understanding cancer is to understand what makes these cells grow.


Estrogen, A Primary Carcinogen

The primary stimulus for the growth of the trophoblast is high estrogen, as occurs during pregnancy. Estrogen is associated with cell proliferation. Modern medicine acknowledges that estrogen is a carcinogen, for which reason estrogen inhibitors are among the drugs used for cancer.

One may ask, why does so much cancer occur in men, or in post-menopausal women who do not produce as much estrogen? The answer is that everyone's adrenal glands and perhaps other sites produce estrogens, in both sexes and at all ages.

Normal estrogen production by the adrenal glands or ovaries is not a problem. The liver converts the potent estrogens such as estrone to a harmless form. However, when the liver is toxic or otherwise compromised, it cannot detoxify estrogen properly. Estrone increases and the stage is set for cancer. Guyton explains the fate of the estrogens as follows:


“The liver conjugates the estrogens … and about one-fifth of these conjugated products are excreted in the bile while most of the remainder are excreted in the urine. Also, the liver converts the potent estrogens, estradiol and estrone, into an almost impotent estrogen, estriol. Therefore, the liver plays an important role in removing those estrogens from the blood. Indeed, diminished liver function actually increases activity of estrogens in the body, sometimes causing hyperestrinism." (Guyton, p.1010) (italics are mine)


Liver toxicity today is the rule rather then the exception. Causes for liver toxicity include:


· Toxins in the food supply. These include toxic metals, pesticide residues, preservatives and thousands of other additives used in prepared foods. Some pesticides and other chemicals mimic the effects of estrogen by occupying estrogen binding sites. This may cause more estrogens to circulate freely in the body. An interesting recent study found that cadmium mimics the effects of estrogen (Nature, August 2003).


· Thousands of organic chemicals and toxic metals in the environment. Besides food, sources of toxins include contaminated air, dental materials, especially silver amalgam fillings, and skin contact with toxins in solvents, detergents, skin care products, chlorinated and fluoridated water and other household and industrial chemicals. Building materials, carpets, plastics and office machinery may also outgas toxic chemicals.



· Radiation exposure damages the liver. Everyone is exposed to some ionizing radiation from bomb fallout, nuclear plant accidents, medical x-rays and other uses of radiation.



· Prescription, over-the-counter and other remedies. Almost all pharmaceuticals are synthetic chemicals that must be detoxified and excreted, primarily by the liver. Drug residues are present even in tap water supplies. Vaccines may be preserved with toxic metals. Many herbs are toxic as well, though much less than most drugs. Vitamin products that contain sea minerals and land-based mineral deposits often contain toxic metals. A portion of any ingested drug or chemical remains in the body, often for years. These will build up and can be an important source of liver toxicity.



· Adrenal exhaustion. This is an indirect cause. Adrenal weakness contributes to a slow oxidation rate and sluggish liver activity. Also, the body compensates for adrenal depletion by accumulating toxic levels of copper, iron, chromium, selenium, manganese, aluminum, cadmium, iron, lead and other metals that are toxic to the liver.



· Nutrient deficiencies. Most people have nutrient deficiencies. These impair the liver's normal detoxification pathways. Nutrient deficiencies are the result of poor quality diets, poor eating habits and impaired digestion. Also, stress increases the need for nutrients.



· Impaired digestion. Poor digestion causes the production of toxic substances in the intestines due to fermentation and putrefaction of food. A vicious cycle occurs in which the toxic liver does not produce enough bile and digestive enzymes. Food is then poorly digested, which generates toxins that in turn worsen the condition of the liver. This further impairs enzyme production, which results in more toxins in the intestines.



· Improper bowel flora such as candida albicans and other pathogenic organisms. These can produce deadly toxins in the intestines. Candida albicans, for example, produces alcohol and acetaldehyde.



· Chronic infections anywhere in the body. Bacterial and other infections generate endotoxins and exotoxins. Chronic infections are much more common than imagined. I estimate most people have a dozen low-grade chronic infections. Common sites are the teeth, eyes, ears, throat, bladder, bronchials, intestines and skin.



· Stress from any cause activates the sympathetic nervous system, which in turn reduces liver activity. Stress also impairs digestion, which leads to more toxin generation in the intestines.


· Autonomic imbalance, in particular excessive sympathetic nervous system activity. The sympathetic nervous system inhibits the activity of the liver. This is explained below in more detail.



· Fatigue. Fatigue can be an important factor in liver toxicity.


Sauna therapy can be most helpful for many of these imbalances. It helps with detoxification, chronic infections, inhibiting the sympathetic nervous system, decongesting the internal organs and improving circulation. Sauna therapy thus can assist with several mechanisms that inhibit abnormal trophoblast activity.


Reduced Pancreatic Enzyme Secretion

At about 12 weeks of pregnancy, the trophoblast usually stops growing and the placenta takes over the function of nourishing the fetus. Dr. Beard found that enzymes produced by the fetal and maternal pancreas stop the growth of the trophoblast.

This is the basis for the use of pancreatic enzymes in the treatment of cancer advocated by Dr. William Kelley, DDS and others (Kelley, W.D., 1997). Large quantities of pancreatic enzymes are given by mouth, which inhibit the growth of malignant cells.

The pancreas plays another role. Pancreatic enzymes are needed for proper digestion. A weakened, toxic or depleted pancreas contributes to a toxic liver by failing to provide adequate enzymes for complete food digestion. Many people do not produce enough pancreatic enzymes or they overeat, exceeding their digestive capacity. These pancreatic enzymes are not the same as "food enzymes" found in raw food. Ideally, excess pancreatic enzymes are secreted so that any cancer that begins to develop will be destroyed.

Causes for deficient pancreatic activity are similar to the causes of liver toxicity. They include stress, poor-quality diets, poor eating habits, infections and toxic exposures. For this reason, sauna therapy can be most helpful to restore pancreatic activity.


The Role Of The Autonomic Nervous System

An important cause of impaired pancreas and liver activity is excessive activity of the sympathetic nervous system. This branch of the autonomic nervous system is sometimes referred to as the fight-or-flight response system. It prepares the body for a stress response and inhibits the activity of the liver, kidneys, pancreas, intestines and stomach. These are the organs of detoxification and the organs needed to produce digestive enzymes and cancer-fighting proteolytic enzymes (enzymes that digest foreign proteins).

Excessive activity of the sympathetic nervous system is extremely common today. Causes include stress, hurried or busy lifestyles, toxic metals, nutrient deficiencies, some toxic chemicals and negative attitudes such as fear, worry, anger, resentment and guilt. These factors keep the body in a fight-or-flight or sympathetic state.

Many cancer patients have a sympathetic dominant personality. This means they have difficulty relaxing and are often hard on themselves and others. They are often fearful, angry, guilty, perfectionistic, resentful or use other mechanisms that cause the body to remain in a sympathetic state much of the time. People who exercise too much, worry a lot, work too hard or are obsessive often overwork the sympathetic nervous system.

Therapies that inhibit the sympathetic nervous system are marvelous for cancer patients. These include saunas, coffee enemas, colon therapy, pancreatic enzyme therapy and minerals including calcium, magnesium and zinc. Lots of rest, relaxation techniques, meditation, bodywork, biofeedback and other methods are also helpful. – (end of excerpt from Sauna Therapy book.)

For more on this and related topics, read Cancer And Alternative Therapies, The Cancer Pioneers, Stem Cell Therapies and Bone Marrow Transplants on this website.

Source: by Lawrence Wilson, MD




"Similar to trophoblasts. In size and functioning, somatids are similar to Trophoblast Cells, discussed in a separate article on this website."

Source: http://drlwilson.com/articles/SOMATIDS.htm

 

[TreasureVibe]

What if a cancer is an actual unborn child. Soul included. What if the organism sub- or unconsciously actually by nature starts loving the cancer, as if it would do with a child in the womb, and that is one of the reason that it grows and keeps growing? Would a cancer patient require psychological therapy to consciously acknowledge and repeat that it is not an actual child growing that one possibly loves in the sub- or unconsciousness, to therefore stop it from growing and perhaps stopping the patient's body from feeding it?

Both man and wife are programmed to love a child. So it is not exclusive to one gender to ''love your tumor sub- or unconsciously'' causing it to get fed and grow. Both man and woman have the same type of base cells.

Or perhaps one should start loving the cancer in order for it to succesfully dissapear? Reverse psychology? Forgiving and loving a part of ones self?

Is a cancer an escape attempt of the soul, trying to escape from the body? Or trying to escape in a new body?

 

[TreasureVibe]

Human chorionic gonadotropin (HCG or b-HCG)
Human chorionic gonadotropin (HCG or b-HCG) is a hormone that the placenta makes when a woman is pregnant. Certain cancer cells can also make it.

Source: Human chorionic gonadotropin (HCG or b-HCG) - Canadian Cancer Society

 

[jondoeuk]

A newer vaccine based on this will be tested in a PhI trial in those with NSCLC VG-1000 — A Therapeutic Vaccine for Cancer