BIO-CELLULAR RESEARCH ORGANIZATION
 BCRO Fetal Precursor CELL TRANSPLANTATION

 

Contact Us

 Glossary of Terms FPCT Wiki FAQ
 

 

 List of Diseases Treated by
BCRO

Treatment procedure

List of BCRO fetal precursor cell transplants

How to get BCRO treatment

HOME

 

 Treatment of CANCER, AIDS,  Incurable Immuno deficiencies and Autoimmune Diseases by BCRO Fetal Precursor Cell Therapy

Immune deficiency disorders, such as AIDS, chronic weakness syndrome, as well as cancer, and autoimmune diseases, have been a menace of modern medicine, because there has been 

  • not only no known cure, but also

  • no possibility to slow down the progress of such illnesses. 

During the last four years there has been a growing body of peer-reviewed publications reporting on the success of fetal precursor cell therapy in the treatment of many cancers, both solid (such as cancer of colon, etc.), and dispersed (such as leukemias, etc.) 

Cancer is a disease of the whole organism, physical, mental and spiritual, even if still localized, i.e. without metastases. Cancer is a proliferation of cells that became unique by escaping their normal controls which results in an unregulated growth, lack of differentiation, local tissue invasion, and metastases. The growth of cancer is a regression from the differentiated cell to the non-differentiated cell, or from the adult to embryonic stage of development.

All higher organisms start their lives from one fertilized cell. As long as there is no connection to the blood, i.e. there is a lack of oxygen, cells of the developing embryo divide without differentiation. After nidation of the product of conception at morula stage in the endometrium, the oxygen supply develops, and that triggers the differentiation of the up until then uniform embryonic cells into specific tissues and organs. Cancer is a regression to the ‘pre-nidation stage of division without differentiation’.

Disturbed relationship of Krebs cycle, normally providing 80% of energy supply for the human body, to the evolutionary ancient glycolysis, normally supplying 20% of energy, is probably the most important cause of the regression of mature differentiated tissue into the immature, undifferentiated, embryonic, tissue of cancer. When the supply of energy via Krebs cycle drops to such a low level that certain part of the normal tissue begins to cover more than 20% of its energetic needs by glycolysis, that part of tissue switches back to the state of division without differentiation, as it was in the early embryonic stage, and such undifferentiated cells easily transform into malignant ones.

Cancer is a genetic disease on a somatic cell level.

“Genetic mutations are largely responsible for the generation of malignant cells. These mutations alter the quantity or function of protein products encoded by growth-regulating genes that regulate cell division and DNA repair. Two major categories of mutated genes are oncogenes and tumor suppressor genes.

Oncogenes are abnormal forms of normal genes (proto-oncogenes) that regulate cell growth. Mutation of these genes may result in direct and continuous stimulation of the molecular biologic pathways that control cell growth and division. There are over 100 known oncogenes that contribute to human neoplastic transformation, e.g. ras gene encodes Ras protein, that regulates or signals cell division. It is abnormal in 25% of human cancers. It signals cells to divide even though they should not. Regulatory protein p53 prevents replication of damaged DNA in normal cells and promoted apoptosis (programmed cell death)  in cells with abnormal DNA. Inactive or altered p53 allows cells with abnormal DNA to survive and divide. Mutations are passed to daughter cells, conferring a high probability of neoplastic transformation. The p53 gene is defective in many human cancers.

Oncogenes typically result from acquired somatic cell mutations secondary to point mutations from chemical carcinogens, gene amplifications or insertion of viral genetic elements into host DNA.

As many as 350 billion (milliard) cell divisions occur in each human being every day. With each cell division there is a possibility that both regulating daughter cells will be malignant.

Tumor suppressor genes normally suppress the development of cancer by encoding for proteins that suppress cancer initiation and growth. They are inherent genes that play role in cell division and DNA repair, critical for detecting inappropriate growth signals in cells. If these genes become unable to function as a result of mutations, genetic mutations in other types of cells can proceed unchecked, leading to neoplastic transformation.

As with most genes, two alleles are present that encode for each tumor suppressor gene. A defective copy of one gene may be inherited, leaving a human being with only one functioning allele for the individual tumor suppressor gene. If an acquired mutation occurs in the other allele, the normal protective mechanism of tumor suppressor gene are lost, and dysfunction of other protein products or DNA damage may escape unregulated, leading to cancer.”

All above quoted paragraphs are taken from “Merck Manual of Diagnosis and Therapy”, 18th edition, 2006, the ‘bible’ of pharmaceutical industry for physicians. Cancer is a genetic disease, but none of the cancer therapies described in “Merck Manual” is aimed at the treatment of effects of acquired mutations, inactivation of oncogenes, or their reversal to normally functioning proto-oncogenes, or DNA repair of mutated tumor suppressor genes. Genetic manipulations by gene therapy is briefly mentioned, but not the fact that the sole method of gene therapy known to current medicine is the proper kind of fetal precursor cell transplantation. Animal fetal precursor cell transplantation used in human therapy for 80+ years has at all these times played i.a. a role of physiologic gene therapy!

Father of this therapy, Prof.Dr. Paul Niehans, Bern, Switzerland, published extensively on the benefits of such therapy for treatment of cancer. His inaugural speech in 1955 at his introduction to Papal Academy of Sciences in Vatican, the sole non-Catholic ever, was devoted to the subject of cancer prevention by repeated cell transplantation treatments of aging people.

BCRO fetal precursor cell transplantation has been one of the three key components of ‘Drs. V.N.M. Integrative Individualized Pan-Asian Cancer Treatment project.

Cancerous tissue is an immature, developmentally regressed tissue.  Biologically thinking cancer therapists believe that it is more rational to stimulate this developmentally regressed tissue and give it all support necessary for its re-maturation and re-differentiation, because only by re-differentiation it is possible to re-integrate the cancerous tissue back into the normal organization of the body.

Despite some success rate it appears illogical to aim the entire therapeutic effort at destruction of un-differentiated immature cancer cells with treatment methods that damage healthy tissue as well, including the immune system, seriously endanger life of the cancer patient, and violate human rights of most of victims of this dreadful disease by causing unbearable pain and many other side effects for no medically justifiable reason.

Biological component of ‘Drs. V.N.M. Individualized Integrative Pan-Asian Cancer Treatment project’ consists of the following steps individualized for each patient:

1/ Optimization of ecological aspects, nutrition and lifestyle, elimination of  all noxious elements, diet according to the genetic nutritional type of each patient, use of digestive pancreatic enzymes before each meal, etc.

2/ Oxygenation, to increase the participation of Krebs cycle in providing for the energy needs up to the normal 80% level, and that includes physical activity and exercise, various forms of oxygen therapy, including hyperbaric oxygen, oral hydrogen peroxide, as well as an improvement of enzyme function of all metabolic pathways, including the respiratory electron transport chain in mitochondria, by BCRO kind of fetal precursor cell transplantation, along with oral intake of all co-enzymes required by the body metabolism, e.g. mega doses of vitamins and minerals, etc.

3/ BCRO kind of fetal precursor fetal precursor cell transplantation, that directs de-differentiated cancerous cells back toward natural re-maturation. The effect of such fetal precursor cell transplantation is tumor-specific and dose-dependent, i.e. primary malignant cell determines the choice of cell type to be used for cell transplantation.

4/ BCRO kind of fetal precursor cell transplantation for direct stimulation of the immune system that has failed its function of  immune surveillance, commonly as a result of previous orthodox cancer treatments, (as it is virtually impossible today that the cancer patient seeks help of the practitioner of biologic cancer therapy first).

5/ Implantation of BCRO kind of cytotrophoblastic cells of chorionic villi eliminates blocking factors from the blood of cancer patient.

6/ In some instances, selective stimulation of T-cell activity by transfer factor, implantation of dendritic cell or dendritic cell vaccines, passive lymphocyte transfer, etc.

7/ In emergency situations, lowering the cancer cell count by plasmapheresis: the fewer   cancer cells are present in the body of a patient, the greater is the chance of success of cell transplantation treatment.

BCRO fetal precursor cell transplantation has to be repeated at different intervals, i.e. therapeutic program is individualized to fit the condition of a patient.

The biological cancer therapy must be combined with modified orthodox treatment of cancer that serves the purpose of cyto-reduction of cancer cell mass:

1/ Surgery is limited strictly to the excision of the necrotic center of the tumor.  This ‘debulking’ is quite important at the beginning of cancer treatment to get rid of the ‘biologically dead’ tissue, that is indeed dead if you would measure its electromagnetic field. The dead tissue is beyond the reach of any treatment. Radical excision with wide margins of healthy tissue must be avoided. It should be noted that old experts of German zellentherapie believed that cancerous growth of stomach, pancreas, gallbladder and prostate, should never be operated upon.

Cell transplantation is recommended even in cases of inoperable cancer as it significantly improves the tolerance of cytostatica, inhibits the formation of metastases postoperatively, or decreases their size up to a complete regression.

2/ Radiation must be avoided except when ‘debulking’ is necessary in cases of the advanced dissemination of cancer of hematopoietic and lymphatic systems, when the diagnosis was established too late and spread of cancerous cells became massive, so that the normal cells of these, and other tissues, are ‘suffocated’ by cancerous cells.

Radiation treatment decreases the effectiveness of fetal precursor cell transplantation against cancer, but not as much as chemotherapy.

Treatment of cancer by BCRO kind of fetal precursor cell transplantation prevents the weakening of the immune system caused by chemotherapy and radiotherapy via its immunostimulatory effect.

3/ Chemotherapy must be used in lower dosage that does not destroy immune system and other healthy tissues, and does not intoxicate the patient. During chemotherapy the anti-cancer effect of fetal precursor cell transplantation is noticeably decreased, particularly of cytotrophoblastic cells. After high dose chemotherapy, BCRO kind of fetal precursor cell transplantation should be delayed for 4 – 6  weeks.

There is a growing number of reports in peer reviewed journals from the leading oncologic centers on the success of new therapeutic protocols that encompass conservative cancer surgery, radiation therapy limited to a total of 30 Gy, chemotherapy of a dosage dosage decreased by 70%, and BCRO type of fetal precursor cell transplantation.

Today there are hardly any patients with cancer that received treatment in accordance with above rules. All cancer patients that have ever had cell transplantation, have had it after the standard oncologic treatment failed to control their disease and they began to desperately look for something else to save their life. Majority of such patients are still undergoing some form of standard oncologic treatment at the time of their consultation with cell transplantation expert.

It is difficult to impossible to combine the traditional (‘slush and kill’) orthodox cancer therapy with the biological treatment:

a/ Fetal precursor cell transplantation must not be used while the patient is taking chemotherapy up until the effect of medications subsides, or when the patient is scheduled to  be treated by  chemotherapy before the implantation of fetal precursor cell transplants, because cytostatica damage implanted cell transplants.

b/ For the same reason there must be 2 – 4 weeks interval between the implantation of fetal precursor cell transplants and beginning of radiation treatment, or between the completion of irradiation and implantation of cell transplants.

In this situation it is extremely difficult to create a workable treatment scheme, particularly for patients with advanced cancer, or those with complications of cell destructive therapies.

Julius Cohnheim, an assistant of Rudolf Virchow, the father of modern pathology, proposed in 1877 an embryonic theory of cancer whereby cancerous tumor originated from small clusters of embryonic cells dispersed throughout body, i.e. not differentiated into many different organs or tissues, that remained unchanged during the development of an organism. In other words, cancer cell is an embryonic cell deprived of an ability to participate in normal embryogenesis, or ‘oncogenesis is a blocked ontogenesis’.

In 1902 John Beard published in Lancet "Embryological Aspects and Etiology of Carcinoma", proposing his trophoblastic theory of cancer, whereby cancer is a trophoblastic tissue that deviated from the proper development by departing from the placenta and dispersing throughout the body.

Similarities between the development of cancer and normal embryonic development have given support to the trophoblastic theory of cancer.

1/ Malignant tumors synthesize and release into blood many embryo-specific and trophoblast-specific, proteins, e.g. α-fetoprotein, carcino-embryonic antigen (CEA), enzymes typical of embryo, and many trophoblast-specific hormones , e.g. chorionic gonadotropin (HCG), etc., as well as immunosuppressive substances that defend the cancer against the host immune system.
2/ Organism’s immune response to cancer antigens is remarkably similar to its response to the  embryonic and trophoblastic antigens.
3/ There are many reports of cross-reaction between embryonic/trophoblastic and cancer antigens. Antigens of the developing embryo and trophoblast have exactly the same properties.
4/ Cancer is a ‘pathologic embryo’, which copies the immune reactions occurring during pregnancy.
5/ The biochemical similarities of cancer and embryonic cells have been recognized for many years.
6/ Cytoplasm of cancer cells has an embryonic type of organization.
7/ Cancer cells copy the key biologic mechanism, i.e. ability to reproduce.
8/ Embryo, trophoblast and cancer cells, utilize the same mechanisms to avoid immunologic recognition and lysis by the effector cells of immune system.
9/ Malignant properties of cancerous tumors, i.e. invasive growth, unrestricted rapid mitoses, metastases, are all natural functional characteristics of normal trophoblast development. Trophoblast components are inevitable for any malignant tumor.

Task of treatment of cancer is to create the type and level of immune reactions characteristic of a spontaneous abortion. How to accomplish it in clinical practice?

Pregnancy is a state of natural parabiosis, i.e. tolerance between two genetically different organisms. Establishment of normal pregnancy requires not only mother’s immunologic tolerance to embryo but an active immunological recognition of paternally inherited proteins in the products of conception. The recognition of MHC and MHC-like paternal antigens during pregnancy stimulates the suppressor immunity but not cytotoxic effector immunity. So recognition of foreign antigens is not accompanied by elimination, but by a tolerance of genetically different cells. The more active is such recognition, the stronger the suppression of rejection. Without this, the survival of trophoblast and placenta, and existence of pregnancy-specific immunosuppressive mechanism, are impossible. A deficiency of immunosuppressive mechanism leads to the rejection of fetus, and rejection of cancer as well.

Cancer can be regarded as a disease of immunosuppressive reaction in the organism. Normally, immunosuppression, as for example after organ transplantation, not only suppresses the rejection, it increases the risk of cancer development. Or, pregnancy protects to a degree against carcinogenesis. Appearance of cancer in human fetuses or newborns is extremely rare.

Immunosuppression during pregnancy is accomplished through the joint activity of maternal lymphocytes and humoral products of fetal and placental origin. Even though the fetal portion of placenta is not genetically identical to the maternal portion, placenta is not ever rejected by mother. Paternal MHC antigens of fetal portion of placenta are not targets for maternal lymphocytes.

There are tumor products recognized by the host’s immune system that do not cause tumor rejection. It is due to induction of suppressor T-lymphocytes, decreased level of T-helpers, and autologous serum blocking factors in cancer patients. Recognition of tumor antigens by the patient’s immune system occurs simultaneously with suppression of effector mechanisms of cell immunity by serum blocking factors. Cancer is a pathologic process capable of neutralizing any number of cytotoxic lymphocytes. 

Therapeutic anti-cancer effect can be achieved by inhibition of immunosuppressive properties of embryo-like functions of malignant cells. In other words, besides a general augmentation of the host’s immune system, which may weaken to the level of a total anergy in the patients with advanced metastatic cancer, it is mandatory to destroy the ‘immunity’ of the cancer. Destruction of cancer immunity is most important particularly in the early stages of cancer when the immune system still functions well, so that there is no need to support it.

Stimulation of function of T-lymphocytes does not decrease the activity of immunosuppressive products released by cancer.

Common feature of immune reactivity in pregnancy, and in cancer, is the presence of characteristic sensitization to embryo antigens and inhibition of such reaction by serum.  While endogenous immunosuppression serves to protect the embryo in pregnancy, such suppression supports the pathological process in cancer by distorting the effector immunity. Without eliminating such immunosuppression it is difficult to inhibit the growth of malignant tumor.

Anti-immunosuppression effect can be achieved by transplantation of cells with a high concentration of blocking substances, found for example in cytotrophoblastic cells of chorionic villi, a homogenous epithelium with frequent mitoses, relatively poorly differentiated, developing before syncytiotrophoblast, a layer with rare mitoses, and a lack of MHC antigen.  Cytotrophoblasts effectively block all reactions of cell immunity. Implantation of cytotrophoblastic cells of placenta triggers the production of anti-suppressive antibodies by B-cells of cancer patient, which neutralize many embryo-like products of cancer cells. Such antibodies form complexes with serum blocking factors, immunosuppressive agents fixed on circulating lymphocytes and cancer cells. The complexes  of anti-suppressive antibodies and serum blocking substances are eliminated from the organism, and that arms the effector lymphocytes of the patient. Neutralization of the suppressor products on the surface of cancer cells makes them more vulnerable targets for NK cells and cytotoxic lymphocytes.

Implantation of cytotrophoblastic cells causes a direct anti-cancer effect. By weakening the protective mechanisms of cancer, or tumor immunity, the host’s effector immunity realizes its anti-tumor potential with less difficulty.  The greatest de-blocking effect is due to antibodies against humoral suppressor products, antibodies against suppressor lymphocytes, and activation of counter-suppressors.

Now about the third component of ‘Drs. V.N.M. Individualized Integrative Pan-Asian Cancer Treatment project’: electric therapy.

 

Autonomous nervous system regulation guided by bio-impedance /conductance

Western medicine has always directed its scientific interest to the matter, and ignored the study of energy in the living body. On the contrary, the eastern medicine has devoted for several millenia its full attention to the investigation of energy, and to the correction of abnormal flows of energy by various therapeutic methods, in particular acupuncture.

In the course of 20th century western physicists elucidated the nature of energy, and its relationship to the matter, but paradoxically this knowledge has had no influence on the official medical thinking in the West. Now we know that space and time is one continuous matter, and that the matter can be instantly changed into energy and reverse. Particles of the matter are actually waves of energy that behave as particles under certain conditions.

When we compare any living body 30 seconds before death and thirty seconds after death, there will be a dramatic difference in energy flows. The easily detectable energy in the body before death disappears at the moment of death. Energy flow is obviously a cardinal feature of life. Lawyers recognized that but not so physicians. Determination of the moment of death by medical examination, in other words by observation of the matter, is frequently very difficult, and for that reason in most western legal systems the death is defined as an absence of brain waves by electroencephalography, or absence of any detectable energy flow in the brain.

Energy flow in the living body

‘Eastern’ medicine has always believed that bio-energy, or vital energy, or Chi of Chinese medicine, control  all physical processes in the living body, and that abnormalities of energy flow precede any observable pathological changes in the matter by days, months, even years.

Since official ‘western’ medicine accepted (‘eastern’) Chinese acupuncture more than three decades ago, it is about time to acknowledge the discoveries of ‘western’ non-linear physics, which serve as the basis of ‘quantum medicine’ (such technical term is still largely unknown but it clearly indicates the association with ‘quantum theory’ of modern physics).

One of the key discoveries of quantum medicine was that each higher living organism reacts to individual electromagnetic quanta, and resonates with a frequency that is characteristic for that organism. Such electromagnetic signals (quanta) are transmitted within a living organism as polarized waves, along the high-molecular conductive chains (peptide networks with hydrogen bridge links), which coincide with the meridians of Chinese acupuncture.

Technological advances after WW2 made it possible to measure very weak electric currents and to prove the validity of over two thousand years’ old Chinese theory of acupuncture which states that there is a continuous flow of bio-energy along the meridians. The resistance and conductance of the energy flow along these meridians can be measured at their end points, and at the specific points along their course, wherever they run close to the skin surface. These ‘acupuncture points’ can be identified by acupuncture needle, but more reliably, by direct or alternating currents, and stimulated. Such stimulation by application of test DC (direct current) or AC (alternating current) along various meridians allows to measure bio-energetic conditions of the whole system, and from such data to establish a diagnosis of the pathological condition of a patient, and ultimately to alleviate the diagnosed abnormality by appropriate electric therapy of the regulatory mechanisms, which in turn control all biochemical functions.

According to Chinese medical thought the initial phases of illness are associated with imbalance of energy flows between yin and yang, first in general, next within a particular meridian, then in the following phase regulatory functions disintegrate, and subsequently a malfunction of involved organ(s) becomes apparent. The structural damage of the involved organs becomes evident after some time only, which can be days, weeks, months, or years. Only at that point will western medicine recognize such a disorder as a disease. In other words, an abnormal energy flow means an impairment of function leading after a period of time to a disease, but when the energy flow is normalized, or ‘balanced’, the state of health is re-established. When toxins, or various pathologic deposits, cause interference with, or interruptions of, polarized waves, electric therapy will re-establish a normal flow, and thereby correct mechanisms responsible for control of faulty biochemical processes.

The ability to measure weak electric currents after WW2 was the basis for a replacement of acupuncture in 50-ies and 60-ies by electro-acupuncture, which also eliminated the need for the piercing of skin. The next stage of technological development brought us a computerized electro-acupuncture.

Every acupuncture point that demonstrates abnormal bio-energy flow can be treated by applying to it AC of saw-tooth waveform of ultra low frequency ~10Hz. The effect of such one time ‘short term therapy’ will last several hours. Ideally the electro-acupuncture treatment should be carried out at least twice a day. In the end, the repeated electro-acupuncture treatments will succeed in breaking the vicious cycle of the disease, stop its progress, so that body’s self-healing powers can take over, and the twice a day repetition of electro-acupuncture therapy will no longer be necessary, just the occasional maintenance treatment .

Besides limiting errors on the part of acupuncturist, and assuring reproducibility of measurements, computerized electro-acupuncture allows instant statistical manipulation of data, and thereby a dynamic, continuous in time, diagnosis, as well as the therapy, of large segments of the body, or of the control mechanism of the entire organ system. The degree of sophistication or complexity is almost unlimited, so that eventually data become comprehensible only to the computer, and not to the treating physician lacking a high level computer expertise.

All bio-resonance instruments work in the following way. After their attachment to the patient’s body via surface electrode, they take a set of electric measurements, and process them in order to establish an electromagnetic diagnosis. Next, they treat the patient by electromagnetic energy with characteristics calculated and designed by the instrument itself to correct the imbalance of bio-energetic flows of the patient and thereby treat and ultimately cure the illness.

Bio-resonance equipment development has been based on the progress of the computer science. The newer computers permitted an instant processing of a huge quantity of data and a prompt response to them. Newer generations of bio-resonance instruments could take and process measurements from a quarter of the body, or an entire body, at the same time, while the classic electro-acupuncture apparatus could take bio-energy measurements on one meridian only at a time.

Bio-resonance diagnostic and therapeutic instruments enable individual determination of the frequencies of DNA molecules, and other resonators, required for the therapy of a particular patient. Each patient has his / her own resonance spectrum, which means that patient can be treated only by an individually designed bio-energy therapy.

Most of research and development in electromagnetic medicine has been carried out by technical professionals, or by a few physicians possessing adequate technical background. Since medical professionals have been almost completely excluded from this process due to lack of understanding of technical language, and these bio-energetical instruments, once attached to the patient, perform completely independently, without a need for human control, physicians have been reluctant to use them.

Cell Physiology of Cancer Treatment & Cancer Reversal  with Micro-current

Electromagnetic medicine sees human beings as networks of complex energy fields that interface with cell systems. It uses specialized forms of energy, such as electric energy, to positively affect those energetic systems that are out of balance due to a disease with a goal to restore homeostasis and equilibrium of autonomous nervous system by rebalancing the energy fields and energetic dynamics of the organism. This is all based on Einstein’s theory E=mc² and a proof that energy and matter are dual expressions of the same universal substance.

In "Bioelectronics: A study in cellular regulation, defense, and cancer," A. v.Szent-Gyorgy postulated that the cell is a machine driven by energy. He stated that the living system may be permeated by an ‘invisible fluid’, the particles of which are electrons, more mobile than molecules, that carry energy, charge and information, and act as the fuel of life. These electrons help to connect molecules to meaningful cell structures. A.v. Szent-Gyorgy believed that the problem with cancer is not that cells are replicating by   themselves, since replication is natural. The abnormality may be within faulty bio-electronic switching mechanisms, which cannot turn off the replicating process.

Other intracellular structures, including mitochondria with their electron transport chains, can be viewed as tiny batteries or electrical power sources as well. There may be electronic switching and transmission systems within cells and between them.

Guyton in his classic “Textbook of Medical Physiology” discussed the cell membrane as a capacitor. He states that the alignment of electrical charges on two sides of the cell membrane is exactly the same process that takes place when an electrical capacitor becomes charged with electricity. Structure of the cell membrane as the bi-molecular leaflet of phospholipids and sterols with hydrocarbon interior and polar groups at the surface has been proven years ago.

With A. v.Szent-Gyorgy's idea in mind, Becker postulated an analog-coded information system that was closely related to the nerves, located in glial and Schwann cells, i.e. not localized in the nerve fibers themselves, which used semi-conductive direct currents and that, either alone or in synchrony with the nerve impulse system, regulated growth, healing, and other basic processes essential for maintaining health.

Becker’s most astonishing discovery was that, under the influence of an appropriately applied direct current of the more primitive analog system, in the micro-ampere range, certain cells are capable of dedifferentiation. In frogs, mature, fully differentiated cells are able to retrogress to an embryonic form, and then to re-differentiate into whatever cell types are needed to complete regeneration. Humans have limited powers of regeneration because our bodies favor a highly developed digital nervous system of alternating currents, which allows greater abilities of complex motor skills and a conscious thought.

Micro-currents more closely match the analog system of the body. If indeed it is the primitive DC system of the body that control healing ,this may offer an explanation for the documented healing acceleration effects of micro-current treatment.

Over 60 years ago, at the same time that R.Voll published his measurements of weak currents along the Chinese meridians, anatomist R. Burr stated: “The Universe in which we find ourselves and from which we cannot be separated is a place of Law and Order. It is not an accident, nor chaos. It is organized and maintained by an ‘Electro-dynamic field’ capable of determining the position and movement of all charged particles. All living things are molded and controlled by electro-dynamic fields that can be measured and mapped with standard voltmeters. These ‘L-fields of life’ are the basic blueprints of all life on this planet. Measurements of these voltages can reveal physical and mental conditions, thereby allow diagnose illness before symptoms develop, and treat it early.”

An interference field is a local tissue irritation with the potential to cause destabilization of the autonomous nervous system either locally or systemically. Such fields can be found in almost any part of the body.

The purpose of appropriate electric therapy as a component of ‘V.N.M. Individualized Integrative Pan-Asian Cancer Treatment project’ is to eliminate the effect of all interference fields so that the autonomous nervous system of the whole body is restored to a condition of balance as close as  possible, continuously for 5 years, until cancer can be declared cured. The balance of autonomous nervous system means the same as the balance of the bio-energetic flow along the Chinese meridians, i.e. status of health as perfect as possible in the patient with incurable or no longer treatable disease, e,g, cancer..

Autonomous Nervous System Regulation Therapy guided by Computational (artificial) Intelligence

Electrical resistance of tissue with pathology is higher than that of the immediately surrounding area, which is either normal or less abnormal. Regeneration is a series of endothermic, electrochemical reactions. This means that electricity, in miniscule quantities, is needed by the cells to provide energy to fuel the regenerative process.

Diseased organ, organ systems or tissue needs energy in the form of electricity for healing and repair. The patients' body contains more than a sufficient quantity of energy to produce the desired effect, but  the electrical resistance area of pathology is so high that the body's energy flow will not enter the area because the primary laws of physics require that energy travel only via the path of least resistance.

As a result, the electrical energy traveling in the body will circumvent the area of pathology. It will always take the path of least resistance, which is around, rather than through, the area of involvement. To get therapeutic effect we must enable the energy to pass into the area of pathology while still obeying these laws. We can do this by increasing the body's ability to actually produce and store energy in the diseased area.

This is done by charging the tissue like a battery. Tissue cells, just like battery cells, have the ability to hold an electrical charge. The greater the charge on the cell, the less resistant it is to the flow of electrical energy. As the cell charge increases, the molecular kinetic energy in the cell rises. The electro-vibratory rate of the cell's molecular structure must increase with the rising kinetic energy (energy of movement).

A higher electro-vibratory rate will be coupled in direct proportion with an increased electro-conductivity, i.e. decreased electrical resistance. While functioning as a battery, the charged cell provides some of the energy involved in the energy flow equation. the addition of electrical energy to an area of pathology increases the electrical conductivity of the area and hence allows the body's own energy to enter the area and regenerate the tissue.

The term for the quantity of charge that a cell can maintain is ‘capacitance’. As the general health of the cell improves, the capacitance increases. Biologically, the capacitance of the cell is directly proportional to the concentration of adenosinetriphosphate (ATP) in the cell.  ATP is at least partially responsible for binding electrons, which cumulatively represent the electrical charge and usable energy of the cell.

ATP concentration serves a direct vital function in the active transport mechanism known as the ‘sodium pump’. Active transport means that this system, which is directly responsible for the trans-membrane movement of sodium, potassium, calcium, metabolic waste and metabolites, requires large amounts of energy to move vital ions in and out of the cell. Metabolic waste builds up in toxic concentrations when the cell respiration is not in order. The energy which is released when ATP breaks down to ADP fuels the reactions which establish balanced membrane potential gradients and which bring vital metabolites into the cell in exchange for metabolic wastes which are dumped into the general circulation to be detoxified and excreted. What we have when the sodium pump is not functioning is a hypo-polarized, toxic, starving cell.

Cells low in energy, lacking conductance across the cell membrane, are susceptible to cancer and other incurable and untreatable diseases. Normal conductance across cell membrane allows the voltage sensitive ion channels to function appropriately and maintain homeostasis. Metastases are more likely to occur in tissues lacking conductance.

Two German scientists Erwin Neher and Bert Sakmann received Nobel Prize in Medicine and Physiology for elucidating the function of ‘single ion channels’ of cells in 1991.

Re-establishment of the sodium pump occurs when the increase in intracellular current increases mitochondrial function. The increased electro-vibratory rate of the mitochondria enhances the production of ATP in the cytoplasm. The ATP provides the fuel for the transmigration of metabolites and metabolic waste across the cell membrane as well as the reestablishment of cellular ionic concentration gradients. What this means is that cell membrane potential, normally 0.85mV in healthy tissue, is re-established, levels of intracellular metabolic waste, i.e. lactic acid, are reduced and fresh concentrations of usable cellular metabolites are introduced into the exhausted cell. At this point the cell can enter its repair & regenerative phase, with tissue regeneration functions re-established.

Investigations of living cells based on electrical concepts and using electrical techniques have been amazingly successful. The electrical parameters of cellular metabolism are well known and include: resting potential, capacitance, resistance, conductance, impedance, polarization capacity, current density, to name a few.

Ionic current flow pattern between normal and insulted tissue plays an important role in stimulating plasma membrane repair processes, essential to the restoration of that tissue to a normal functional state. The rates at which these processes occur may be accelerated by judicious imposition of an electric current from an outside source.

The current that enters a cell alters the cell membranes voltage in such a way that it allows influx of ions, which can turn on and accelerate biochemical processes essential for cell repair. With direct current only used, the intracellular current would flow only through discrete pores or ion-channels, through a low resistance pathway called tight junctions. If we use pulsed current, there will be an additional pathway for current to enter a cell through membrane capacitance. Current flow through this additional pathway increases the ratio of intracellular to extra-cellular current flow, making the current more effective.

R. Voll was able to chart specific frequencies in the range 0.5 – 10.0 Hz that had pronounced effects on different tissue systems. This very low frequency range, which is resonant with the normal electrical activity of the human body and the frequency of the earth, is the main domain of modern micro-current therapy.

Basic bio-physical research within the last decades has led to the development of autonomous nervous system therapy guided by bio-cybernetics (bio-equivalent stimulation) in the USA, used for treatment of patients since the beginning of 1980’s. The concept is based on the recognition that the bio-physical processes that promote the cell metabolism in humans play a significant role in the regulation of all vital processes.

The bio-stimulation is a vectored motion of carriers of electrical charge or so-called micro current. It is better tolerated than any other form of stimulation and can gently treat tissue and cells. This current is fine-tuned to the level of the normal electric activities of the somatic cells and therefore very natural and effective. Electric voltages of between 10 and 20 mV are normal for the cell membranes of a healthy cell. This is maintained by the energy consuming proton transport at the semi-permeable cell membrane. If disorders of those membrane characteristics of the cell occur, it also influences the protein and energy metabolism of the cell. In the case of chronic irritation of the organism, infections and injuries, it leads to disorders of these physiological processes of the cell.

The biological stimulation effect with bio-electrical therapy begins where the body’s own immune system and repair function fail. The healing process of damaged tissue is shortened with externally applied bio-equivalent stimulation that speeds up the repair or renewal of such damaged cells. This occurs by increasing the ATP production, protein synthesis, and DNA regeneration. Bio-equivalent stimulation normalizes the usual activities between the cells, if they have been damaged. The external application of bio-electrical therapy promotes the production of ATP, protein composition, oxygen saturation, ion-exchange, food absorption, breakdown of toxins and neutralization of the oscillatory polarity of defective cells.

Without energy there is no life. A healthy organism can only function, if it is provided with sufficient energy in the correct form and dosage. The organism and its building blocks, represent an open system and, as such, can receive, transform and release energy. The immune system and repair functions are generally capable of equalizing themselves. If this is not the case, the body requires help from outside.

The energy of food is transformed into ATP. During the ATP breakdown, this energy is released again and drives all reactions in the organism. From a thermo-dynamic point, this expenditure of energy creates order in the cells and in the entire body. If this order cannot be maintained in parts of the body or in its entirety, a disease has evolved. 

Autonomous nervous system regulation therapy guided by bio-cybernetics

Cybernetics constitute the science of control and information, irrespective of whether we are dealing with living organisms or machines.’ (N. Wiener, father of Cybernetics, 1948) Cybernetics are about 'the control and automatic regulation of interlinked and intermeshed processes at a minimum cost in terms of the amount of energy used', without which life would not be possible. Medicine must concern itself like no other discipline with the biological control circuits in the living organism, yet, this new line of thought is only beginning to make a little headway in medicine, and very slowly at that.

Organic structures work by means of control circuits that have evolved and proved themselves over millions of years. Control systems are the systems that respond to and affect internal and external environment of a man. Their dysfunction is a cause of every disease, including cancer.

Cybernetics regard man as the most highly developed of all self-regulating dynamic systems in existence. In man the principle of linear causality (i.e. the straight-line relationship between cause and effect), no longer applies. Instead, the principle applicable to man is that of an intermeshed interactive causality. In any cybernetic system, every subsystem is continuously linked to every other subsystem in a network of reciprocal relationships. Seen in this light, disease is a cybernetic problem, since it is the result of a disturbance of the regulatory functions within the interacting structure of the self-regulating dynamic system that is man, and is due to malfunctions in the transmission and processing of information between individual control circuits within the overall system. Thus, it ought to be the physician’s task to act upon these disturbed or faulty control systems, in particular when cancer is the disease to be eliminated, the most complex of them all.

That’s why the Autonomous Nervous System Regulatory Therapy is one of three key components of “Drs. V.N.M. Individualized Integrative Pan-Asian Cancer Treatment project”.

So perhaps the scientific fact that fetal precursor cell transplantation is the most potent immuno-stimulant known to medicine today - by far - will no longer be one of the 'best kept secrets'. 

Immunological testing has been very crude and thus it is hard to assess the degree of benefit from the immuno-stimulating effect of fetal precursor cell transplants among those ~ 5 million patients treated by fetal precursor cell therapy over the last 70 years. The quick reversal of the condition of dying AIDS patient to a state when he/she can live a normal life, work and look healthy, just 5 weeks after BCRO fetal precursor cell transplantation, is extremely convincing.

Modern medicine has a very limited armamentarium of therapies for immune deficiencies.  With the exception of fetal precursor cell transplants there are no effective direct immuno-stimulants available for treatment of diseases today.  

BCRO fetal precursor cell transplantation stimulates immune system spectacularly well, particularly one that is weakened for one reason or another. 

And that applies to even such deadly diseases of immune system as AIDS, and cancer, in which the immune system has become debilitated as a result of an illness and a method of treatment used to combat it. 

It is therapeutically effective also against autoimmune diseases, apparently functioning as an immuno-modulator in a way that cannot be currently scientifically explained.

  (biocell@stem-cell-transplantation.com)

The survival of a live organism without a defense against harmful factors of the inner and outer world, whether living or non-living, is impossible. 

The defense mechanism which has developed since the inception of life millions of years ago is a complicated and highly organized system which protects the biologic existence of every living being.

Contact with, and defense against, the environment are key properties of life. Intake and metabolism of life-sustaining matters are recognized as fundamental biological features, but the defense against damaging and life-threatening matters is on the same level of importance.

As sophisticated as the immune system is, it operates on a very simple basic principle. It distinguishes 'self' from 'non-self' and attacks 'non-self' with the ultimate goal of removing it from the body. 

Usually this works in our favor, such as when our body is attacked by pathogenic microbes. 

At other times it works against us, such as when our life depends on a transplanted organ: heart, liver or kidney, and our immune system attacks it as 'non-self' and causes its rejection.

One can think of the immune system as a defending army. This army consists of many different battalions, each battalion has to carry out a predetermined activity, and each soldier is ordered to handle a specific task. 

After all, this army has to fight off many kinds of invaders: bacteria, fungi, viruses, tumors, toxins, foreign proteins and every one requires a different battle plan. 

Without such army of immunological soldiers to fight them, operating according to the correct battle plan, we would succumb to the invaders before we would grow out of infancy.

The human immune system consists of three components:

  1. the epithelial surface, protecting us against outside world and the microbial world inside of our own bodies (there are more microbial cells in our body than of our own) - this is historically (phylogenetically) the oldest part;

  2. the reticulo-histiocytary system, spread diffusely throughout our body - this one had historically developed next;

  3. thymo-lymphatic system, consisting of thymus gland, and network of lymphatic vessels carrying lymph, which is filtered in lymphatic nodes, and

  4. spleen, which filters blood, among other functions - these two are the youngest part.

The lymphocytes are the most important cells of the defense system. More than a trillion of them are in the body at once, either circulating in the blood or on guard in the lymph nodes. There are two types of lymphocytes: T-cells and B-cells

Both are formed in bone marrow. B-cells mature in blood, while T-cells must pass through and mature in thymus gland. Thymus, located just behind the upper part of the breast bone, is like a drill sergeant, it instructs the lymphocytes how to recognize 'non-self' and what to do when 'non-self' invades the body.

T-cells are the sentries of our body. When the invader enters the body, T-cells sound an alarm and direct the battle. Through a complicated system they mobilize other lymphocytes and other 'soldiers', such as histiocytes, macrophages, etc., and 'weapons' (complement, cytokines, etc.) to fight the enemy. They also enter the battle directly.

B-cells produce plasma cells, which in turn produce antibodies. This system has a memory. Once a B-cell produced an antibody against a specific foreign antigen, it never forgets how to make it. 

Thus each succeeding wave of the same infection (or other type of antigen) is fought off with an increasing efficiency. This is the basis for immunization and also explains why we fall victim to several childhood infectious diseases only once.

Of course this 'immunological memory' works sometimes against us, too. 

When we are allergic to something - even though the object isn't, in itself, a threat - the body's immunological memory can unleash 'defensive' biochemical weapons and turn it into an illness ranging from sniffles to sudden death by suffocation (anaphylaxis).

Sometimes the immune system fails to recognize even parts of our own body as 'self' and attacks them as 'non-self'. 

This leads to 'autoimmune diseases', such as rheumatoid arthritis, systemic lupus erythematosus, multiple sclerosis, glomerulonephritis, etc., against which there is no real treatment, with the exception of BCRO type of cell transplantation which is therapeutically effective against all autoimmune diseases, apparently by functioning as an immunomodulator in a way that lacks any scientific explanation. It should be done immediately after the diagnosis of an autoimmune disease was made and not to waste time by overdosing patient with symptomatic treatment by cortison and immunosuppressants. 

The defense capabilities of our immune system have a 'life profile'. After 'immuno-tolerance' of the embryonic and fetal stage of life (when the immune system is not functioning and the entire defense depends on the immune system of pregnant mother and placenta), the immune system gradually 'wakes up', until it reaches the optimal functioning level between 10 and 15 years of age. 

During puberty the immune system function will become depressed again, the exact timing depends on the sex.

Afterward the immune system works at full capacity for the next 30 to 35 years. 

During the forties a regression period will inevitably ensue, when the function of immune system diminishes relentlessly until a senile 'immuno-paralysis' period is reached when body becomes defenseless against malignancy and even the most banal infections.

BCRO type of fetal precursor cell transplantation,  has been used successfully for 80+ years as treatment of many diseases
  • for which modern medicine has had no therapy (i.e. incurable), or
     
  • in which 'state-of-art' therapies stopped being effective (i.e. no longer treatable),

in documented over 5 millions of patients worldwide. Physicians can learn about it in a textbook by E. Michael Molnar, M.D.: Fetal Precursor Cell Transplantation, BCRO Fetal Precursor Cell Transplantation", published in 2014 by www.amazon.com
On the same web site the general readership can find out all about it in the book by the same author: “Treatment of Incurable and No Longer Treatable Diseases”, published in January 2015, as well as in his autobiography: “Diseases and Genocide are not Our Destiny”. You can buy it as 'free reader download for PC' as well as Kindle Book.

 

 (biocell@stem-cell-transplantation.com)

 

 
 

  TOP

ABOUT BCRO WARRANTY/REPLACEMENT DISCLAIMER PRIVACY STATEMENT
Copyright Stem Cell Transplantation Ltd.
Updated: March 2015