Deceptology in cancer and vaccine sciences: Seeds of immune destruction-mini electric shocks in mitochondria: Neuroplasticity-electrobiology of response profiles and increased induced diseases in four generations - A hypothesis

Abstract

From Rockefeller's support of patent medicine to Gates' patent vaccines, medical establishment invested a great deal in intellectual ignorance. Through the control over medical education and research it has created a public illusion to prop up corporate profit and encouraged the lust for money and power. An overview of data on cancer and vaccine sciences, the status of Americans' health, a survey of repeated failed projects, economic toxicity, and heavy drug consumption or addiction among young and old provide compelling evidence that in the twentieth century nearly all classic disease categories (congenital, inheritance, neonatal, or induced) shifted to increase induced diseases. Examples of this deceptology in ignoring or minimizing, and mocking fundamental discoveries and theories in cancer and vaccine sciences are attacks on research showing that (a), effective immunity is responsible for defending and killing pathogens and defective cancerous cells, correcting and repairing genetic mutations; (b) viruses cause cancer; and (c), abnormal gene mutations are often the consequences of (and secondary to) disturbances in effective immunity. The outcomes of cancer reductionist approaches to therapies reveal failure rates of 90% (+/-5) for solid tumors; loss of over 50 million lives and waste of $30-50 trillions on too many worthless, out-of-focus, and irresponsible projects. Current emphasis on vaccination of public with pathogen-specific vaccines and ingredients seems new terms for drugging young and old. Cumulative exposures to low level carcinogens and environmental hazards or high energy electronic devices (EMF; 5G) are additional triggers to vaccine toxicities (antigen-mitochondrial overload) or "seeds of immune destruction" that create mini electrical shocks (molecular sinks holes) in highly synchronized and regulated immune network that retard time-energy-dependent biorhythms in organs resulting in causes, exacerbations or consequences of mild, moderate or severe immune disorders. Four generations of drug-dependent Americans strongly suggest that medical establishment has practiced decades of intellectual deception through its claims on "war on cancer"; that cancer is 100, 200, or 1000 diseases; identification of "individual" genetic mutations to cure diseases; "vaccines are safe". Such immoral and unethical practices, along with intellectual harassment and bullying, censoring or silencing of independent and competent professionals ("Intellectual Me Too") present grave concerns, far greater compared with the sexual harassment of 'Me Too' movement that was recently spearheaded by NIH. The principal driving forces behind conducting deceptive and illogical medical/cancer and vaccine projects seem to be; (a) huge return of investment and corporate profit for selling drugs and vaccines; (b) maintenance of abusive power over public health; (c) global control of population growth via increased induction of diseases, infertility, decline in life-span, and death. An overview of accidental discoveries that we established and extended since 1980s, on models of acute and chronic ocular inflammatory diseases, provides series of the first evidence for a direct link between inflammation and multistep immune dysfunction in tumorigenesis and angiogenesis. Results are relevant to demonstrate that current emphasis on vaccinating the unborn, newborn, or infant would induce immediate or long-term immune disorders (eg, low birth weight, preterm birth, fatigue, autism, epilepsy/seizures, BBB leakage, autoimmune, neurodegenerative or digestive diseases, obesity, diabetes, cardiovascular problems, or cancers). Vaccination of the unborn is likely to disturb trophoblast-embryo-fetus-placenta biology and orderly growth of embryo-fetus, alter epithelial-mesenchymal transition or constituent-inducible receptors, damage mitochondria, and diverse function of histamine-histidine pathways. Significant increased in childhood illnesses are likely due to toxicities of vaccine and incipient (eg, metals [Al, Hg], detergents, fetal tissue, DNA/RNA) that retard bioenergetics of mitochondria, alter polarization-depolarization balance of tumoricidal (Yin) and tumorigenic (Yang) properties of immunity. Captivated by complex electobiology of immunity, this multidisciplinary perspective is an attempt to initiate identifying bases for increased induction of immune disorders in three to four generations in America. We hypothesize that (a) gene-environment-immune biorhythms parallel neuronal function (brain neuroplasticity) with super-packages of inducible (adaptive or horizontal) electronic signals and (b) autonomic sympathetic and parasympathetic circuitry that shape immunity (Yin-Yang) cannot be explained by limited genomics (innate, perpendicular) that conventionally explain certain inherited diseases (eg, sickle cell anemia, progeria). Future studies should focus on deep learning of complex electrobiology of immunity that requires differential bioenergetics from mitochondria and cytoplasm. Approaches to limit or control excessive activation of gene-environment-immunity are keys to assess accurate disease risk formulations, prevent inducible diseases, and develop universal safe vaccines that promote health, the most basic human right.

Keywords: Gates vaccines; HPV; Rockefeller medicine; Yin and Yang of immunity; adjuvant; aluminum; antigen overload; autism; autoimmune disease; cancer bioenergetics; constituent and inducible receptors; deceptology; fetus tissue; gene-environment-immune; genomics; glyphosate; histidine-histamine; hypoxia; immune-privileged; immune-responsive; inflammation; intellectual harassment; mercury; mini electrical shocks; mitochondria; molecular sink holes; neurodegenerative diseases; pathogen-specific vaccines; philanthropists; placenta; policy makers; therapy; trophoblast; tumoricidal; tumorigenic; vaccine incipient.

FIGURE 1

Schematic representation that current pathogen‐specific vaccines and incipient given to unborn (fetus), newborn or infant (age 0 to 24 mons), toddler or children (2‐16 years) are causes, exacerbations (aggregations) or consequences of development of a wide range of immune disorders that are often features of age‐associated chronic illnesses. Vaccination of unborn is depicted to lead to SIDS, preterm birth or low weight at birth, and associated underdeveloped immunity as bases for increased mortality and induction of childhood diseases. It depicts that current vaccines and metal‐containing ingredients are seeds of immune destruction, particularly affecting mitochondria and oxido‐redox potentials and immune‐metabolic‐hormonal‐neuronal activities. The scheme also represents that current vaccines and incipient shift/increase the classic categories of disease (inheritance, congenital, neonatal, and induced) to induced diseases. See text

FIGURE 2

Schematic representation that inflammation and aging are co‐risk factors in developmental phases of immune dysfunction in multistep tumorigenesis and angiogenesis. The left panel depicts initial stages of our ‘accidental’ discoveries on inflammation‐induced identifiable immune dysfunction in ocular tissue responses during (a) acute phase responses or self‐terminating inflammation (reversible); (b) intermediate phase, down‐regulation phenomenon accompanied with mild tissue atrophy and neovascularization (potentially reversible); and (c) chronic phase, induction of massive lymphoid hyperplasia and tumorigenesis and angiogenesis (irreversible?). The right panel represents chronic inflammation and continued stages of tissue growth (d,e), advancing to cancer malignancies and angiogenesis in site‐specific tissue. The complex scheme demonstrates that majorities of translational medicine and clinical trials are conducted in identification of endless damaged molecules at advanced stages of carcinogenesis for drug development and therapy (red arrows in phase e, ‘cancer tsunami’). Modified from Exp Opin Biol Ther; Informa Healthcare, 2011. ⁴⁷ All Rights reserved

FIGURE 3

Schematic representation of toxicities of vaccines altering fetus growth and development and bases for immediate or long‐term immune disorders, at different stages of life. The complex scheme represents that current pathogen‐specific vaccines (MMR, Hep, Flu, dTab, HPV, meningitis) and adjuvants [Al, Hg, detergents, solvents growth factors (PS80, Silica A, fetal serum)] would alter immune electromagnetic response profiles in tissues and damage differential bioenergetics of mitochondrial oxidative phosphorylation, leading to diverse immune disorders. It also depicts that vaccination of unborn/newborn and infants lead to shifted disease categories (congenital, hereditary, neonatal or induced) to increase the induced diseases (black box). See text

FIGURE 4

Schematic representation of toxicities of vaccines and incipient in altering mitochondrial function and diverse activities of histidine‐histamine pathways toward increased induction of diseases. Vaccine incipient/excipient (eg, metals, growth factors, DNA/RNA, and fetal tissues) are depicted to alter immune‐neuronal response dynamics, influencing genomic, mitochondrial, metabolic, and physiological functions of gastric secretion, energy levels (ATP/ADP), cell cycle and brain activities as well as vasculature, tissue growth or necrosis. The scheme depicts that 140–200 genes are involved in histamine‐histidine metabolic‐neuro‐immune pathways. Altered tissue bioenergetics is depicted to cause induction of mild, moderate, or severe immune disorders (black box). The scheme also represents that current vaccines shift the incidence of all classically known diseases (congenital, hereditary, neonatal, or induced) to increase the level of induced diseases. See text

FIGURE 5

Schematic representation of toxicities of metals and other ingredients in pathogen‐specific vaccines in induction of mild, moderate, or severe immune disorders. Metals such as aluminum (Al) or mercury (Hg) are depicted to compete with essential trace elements and alter tissue biological activities (see blue box and center divided circle), influencing mitochondrial bioenergetics metabolism and immune response profiles in tissues. The scheme depicts that vaccines and ingredients differentially influence tissues that are immune‐privileged (brain, CNS, reproductive organs) or immune‐responsive (epithelial, endothelial, mucus, fibroblast) in the genesis of wide ranges of immune disorders (tissue necrosis or growth). See text