Documented Proof Psychiatric Drugs Shorten Life Span
By Shemuwel Moser
No longer is involuntary drugging only a concern to those locked away in an institution. "Laws quietly passed in 36 US states now allow the government to court order you to take psychiatric drugs, even though you're law abiding and living at home, in your own neighborhood. These court orders are known as "Involuntary Outpatient Commitment" (IOC). Typically, you'd be required to report to your community mental health center every few weeks for a "depot injection" of a "neuroleptic drug" such as Prolixin or Haldol in your butt. These drugs are time released [in a base of oil and injected intramuscularly], so that the super-powerful impact lasts weeks until your next injection. The court orders can be routinely re-approved, so these injections can go on for years." Reports Support Coalition International http://www.mindfreedom.org .
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Disclaimer: Many of the
statements that follow in this report (Namely the effect that neuroleptic drugs
have on the duration of life span and sense of well being.) have not been
investigated or evaluated by the FDA (so they claim) nor do they care to. The
FDA does not even require animal studies to determine how these drugs affect the
duration of life span which is shocking considering that the FDA is supposed to
be charged with protecting the American people. The conclusions in this report
are based on available facts, for which a positive assertion can be made by
putting the information together so that the true nature of these drugs can be
established. This information is what the FDA, psychiatrists, and the
pharmaceutical companies do NOT WANT YOU TO KNOW. This information is both
shocking and scandalous and reveals a probable conspiracy so be warned. The
common people that are affected by this are not supposed to be smart enough to
understand and figure it out, but I have.
The purpose of this report is to prove conclusively that neuroleptic drugs (Also know as antipsychotics or antipsychotic drugs, tranquilizers, psychotropics or psychotrophics, or psychotropic drugs or psychotrophic drugs) shorten life span, destroy sexual function and fertility, take away sense of well being which can precipitate suicide and or violent behavior etc. This will be established in this discussion through a rudimentary explanation of some facets of biochemistry and by quoting reputable sources. Also to empower the people who may be affected by this with knowledge that they can use to defend their rights and help overturn these laws as unconstitutional and as basic human rights violations. Also to help educate people who have friends and or family members who are affected by this and to provide understandable information to the general public who are being denied the facts.
These drugs are not just given to those labeled as "schizophrenic" or said to be "psychotic" or have "psychosis" or have "schizophrenia". These drugs are often given to people with depression, manic depression or bipolar disorder, mania, Alzheimer’s patients or those suffering from Alzheimer’s Disease, people with brain damage or head injuries, retarded children and adults, many children with Attention Deficit Disorder or ADD or ADHD and children and teenagers who simply have a hot temper (which ironically the drugs will make worse) as well as many other things. If you are unsure whether a certain drug is a neuroleptic or not then here is a list of many names for neuroleptic drugs.
List of neuroleptic drug names: Chlorpromazine, (Brand names are as follows; Chlor-PZ, Klorazine, Promachlor, Promapar, Sonazine, Thorazine, Chlorprom, Chlor-Promanyl and Largactil) Fluphenazine, (Brand names are as follows; Permitil, Prolixin, Modecate, Moditen) Mesoridazine Besylate, (Brand name is Serentil) Perphenazine, (Brand names are as follows; Trilafon, Etrafon, Triavil, Phenazine and Etrafon) Prochlorperazine, (Brand names are as follows; Compazine and Stemetil) Promazine Hydrocloride, (Brand name Sparine) Thioridazine, (Brand names are Mellaril, Novoridazine and Thioril) Trifuoperazine, (Brand names are as follows; Stelazine, Clinazine, Novaflurazine, Pentazine, Terfluzine and Triflurin) Clozapine, (Brand named Clozaril, in Germany called Leponex) Haloperadol, (Brand name Haldol) Loxapine, (Brand name Loxitane) Pimozide (Brand name is Orap) Thiothixene, (Brand name Navane) Risperidone (Brand name Risperdal), Zyprexa (Brand name is Olanzapine), Sertindole, Ziprasidone (Brand name Geodon or Geodone was planned to be named Zeldox), Amperozide, Remoxipride, Melperone, Zotepine, Isofloxythepin, Setoperone, Perospirone, Quetiapine (Brand name Seroquel)Methotrimeprazine (Brand name Nozinan or Nosinan, called Levomepromazin in Germany), Zuclopenthixol (Brand name Clopixol), Zuclopenthixol Acetate (Brand name Clopixol Acuphase), Amisulpride (Brand name Solian). Also the antidepressant drug Sertraline (Brand name Zoloft) is molecularly indistinguishable from that of the neuroleptics and has even been tried as a neuroleptic. This list contains generic names and many brand names used in the USA and Canada. This list is by no means comprehensive. Please help provide the names used in other countries by E-mailing me at: email@example.com.
The compulsory administration of neuroleptic drugs by order of the state is not only a violation of one's right to liberty but also the right to life and the pursuit of happiness. The right to life because neuroleptics shorten life span and the precipitous onset of degenerative disease that these drugs induce. The right to the pursuit of happiness because neuroleptics take away sense of well being. The right to liberty because of not being able to make ones own decision regarding the administration of these drugs and the right to freedom of religious worship when the administration of these drugs precludes their use when it violates one's religious values and convictions. For legitimate religious grounds to refuse these drugs see Footnote C below.
The compulsory administration of neuroleptics because of state order is a violation to one's right to life because the drugs not only shorten life span but also make the quality of one's life inferior due to the precipitous onset of degenerative disease that these drugs induce. This is not a statement unsupported by fact. Let me now explain.
Dopamine, norepinephrine, and epinephrine all belong to the class of neurotransmitters called catecholamines. Catecholamines are synthesized from the amino acids L-Phenylalanine and L-Tyrosine. This is the complete step by step synthesis of these substances: L-Phenylalanine --> L-Tyrosine -- > L-DOPA --> Dopamine --> Norepinephrine --> Epinephrine. L-Tyrosine is also converted to the thyroid hormone thyroxine by the thyroid and dopamine is also converted to the skin pigment melanin.
Serotonin is a neurotransmitter that is synthesized from the amino acid L-Tryptophan. Melatonin the sleep-inducing hormone produced by the pineal gland is synthesized from Serotonin. Here is the complete step by step synthesis of these substances. L-Tryptophan --> 5-Hydroxy - L-Tryptophan (5-HTP) --> 5-Hydroxy - L-Tryptomine (Serotonin) --> Melatonin (O-methyl - N - Acetylserotonin).
The main function of neuroleptics is blockage of catecholamines in the brain. They have greatest affinity for dopamine receptors and to a lesser extent norepinephrine and epinephrine. (A future report of mine will prove that these drugs destroy dopaminergic receptors. See Footnote B for a simplified explanation of this.) Neuroleptics block dopamine receptors in the brain with generally greatest affinity for D1 and D2 receptors. Dopamine is a neurotransmitter and a receptor is the "keyhole" which dopamine like a key, plugs into for neuronal communication. There are many other neurotransmitters, all with their respective "key holes" or receptors. But the analogy of a "keyhole" is insufficient because there are different receptors that fit their corresponding neurotransmitter. Different sides of the neurotransmitters will fit into the different types of receptors. It is like the fact that a puzzle piece has different sides with different shapes. It's the different sides of the neurotransmitter that fit into their corresponding receptors. Since these neurotransmitter molecules are three dimensional in shape, the different sides of its shape fit the different receptors.
When a dopaminergic neuron fires, it releases dopamine into the synapse from vesicles within the presynaptic dendrite. The synapse is a gap or space between dendrites, which are branches off the neuron and a presynaptic dendrite is the dendrite that releases the neurotransmitter. Think of this gap as if it were the gap of a spark plug in an automobile except it is not electricity that fires within this gap it is a chemical messenger; a neurotransmitter. This dopamine then binds with dopamine receptors on postsynaptic dendrites, which are the dendrites on the other end of the gap that are the recipient of the neurotransmitter that branch off another neuron. The neurotransmitter then floats within the synapse and through quantum mechanics is drawn to the postsynaptic receptors on the end of the other dendrite where they bind activating ion pumps. Ion pumps are tubular molecular machines made up of amino acid building blocks, which is a protein. Ion pumps are also called channels. These receptors surrounding the circumference of the ion pump cause this ion pump to dilate when activated by the stimulating neurotransmitter dopamine which allows electrolytes to pass through the cell membrane causing an electrical shift in polarity which causes the neuron to fire an electrical charge down its axon. When the electrical charge reaches the other end it causes dopamine to be released from that neuron’s presynaptic dendrites and the process continues in a cascade.
The neurotransmitter Serotonin is an inhibiting neurotransmitter that mediates the expression of the stimulating neurotransmitter Dopamine. There are third dendrites from neurons of the serotoninergic system utilizing this inhibiting neurotransmitter serotonin that act as variable switches at different points within the dopaminergic system. If serotonin is being released into a synapse from a third dendrite where dopamine had just been released, this inhibiting neurotransmitter then acts as a chemical straight jacket by binding to serotoninergic receptors on these same ion pumps which mediates the degree to which dopamine will cause this neuron to fire its electrical charge. This is the simplified relationship dopamine has with serotonin. There are many other neurotransmitters both stimulatory and inhibitory that act in many complex ways that have yet to be understood by science up until this point in time. (For instance the neurotransmitter GABA (4-AminoButyric Acid) is another inhibiting neurotransmitter that has a mediating effect on the stimulating neurotransmitter Glutamate and also has a mediating affect on the stimulating neurotransmitter dopamine in some dopaminergic pathways. The seizure drug Valproic acid or Valproate (brand name Depakote or Depakane) is often prescribed for "mania" or "manic psychosis" and Bi Polar disorder also known as manic depression. Depakote causes an increase in GABA in the brain by inhibiting the two enzymes that are involved in breaking down this neurotransmitter.) Many newer neuroleptic drugs bind with both dopamine and serotoninergic receptors. These serotoninergic receptors are activated continuously by these drugs while at the same time blocking normal serotoninergic function, greatly inhibiting dopaminergic expression.
Neuroleptic drugs block dopamine receptors in all areas of the brain for the types of receptors they have affinity for. Antagonism of a type of receptor is not neurological pathway specific and antagonizes all receptors of the type it has affinity for without regard for the actual function of the neurological pathways they affect. Most dopaminergic function takes place within the limbic system of the brain. (See the article in the magazine called "American Scientist" March-April 1996 Volume 84 called "Reward Deficiency Syndrome" on pages 134 and 135 for an explanation of the limbic system and how it relates to the "reward cascade" which I will discuss later in this report. Click Here for the Article Online )
The limbic system of the brain contains a structure called the hypothalamus. This area of the brain called the hypothalamus is responsible for the regulation of pituitary hormones by the release of controlling hormones. The pituitary is a small gland located at the base of the brain just under the hypothalamus. The pituitary in turn regulates all other bodily hormones. See the book "Facts and Comparisons" III W. Port Plaza, Suite 300 St. Louis MO. USA 63146-3098 (telephone 314-216-2100 or 1-800-223-0554). (Note this book is currently used by Rite Aid Pharmacies in the USA as a reference aid and it is a loose bound updatable book. The updatable section called "Antipsychotic Agents" is (c) 1990) This book states under "antipsychotic agents" that "Antipsychotics block postsynaptic dopamine receptors in the basal ganglia, hypothalamus, limbic system, brain stem and medulla... The phenothiazines appear to act at both D1 and D2 receptors, whereas haloperidol appears to act primarily at D2 receptors." ("D" here stands for dopamine and each different receptor is numbered.) Also see the book "Drug Info for the Health Care Professional 17th edition volume I 1997" by Authority of the United States Pharmacopeial Convention, Inc. (c) 1997 by The United States Pharmacopeial Convention Inc. printed by Rand McNally, Taunton, Massachusetts. Distributed by USPC 12601 Twinbrook Parkway, Rockville, Maryland USA. This book states on page 2321 in the section on phenothiazines under the subheading "Mechanism of action/Effect" that neuroleptics "block postsynaptic mesolimbic dopaminergic receptors in the brain... and depress the release of hypothalamic and hypophyseal hormones." Hypophyseal hormones are pituitary hormones.
One hormone the hypothalamus produces is TRH (thyrotropin releasing hormone or thyrotrophin releasing hormone). This hormone when released by the hypothalamus stimulates the release of the pituitary hormone TSH (thyroid stimulating hormone also called thyroidea stimulating hormone, thyreotropic hormone, threotrophin hormone, TTH, thyrotropin, thyrotrophin). TSH in turn when released by the pituitary stimulates the production or release of the thyroid hormone thyroxine which is abbreviated T4 (four because this is the number of iodine atoms the hormone contains). Thyroxine is the hormone that regulates bodily metabolism. Lowering metabolism by lowering the body's capacity to produce thyroxine shortens life span. See the book "Handbook of Vitamins, Minerals and Hormones 2nd Edition" by Roman J. Kutsky, Ph.D. published by Van Nostrand Reinhold Company New York (c)1973. On page 369 in this book under "Essentially for Life" it states "Deficiency" of thyroxine "in adult shortens life span". Also on page 367 of this book in paragraph three it states that the capacity to produce this hormone is associated with aging. And on page 371 under "Deficiency Symptoms" where it states among other things that deficiency of thyroxine causes "Decreased BMR" (BMR is the abbreviation of Basal Metabolic Rate), "Increase in blood lipid and cholesterol" (lipid is fat). Also see the book "Fats that Heal Fats that Kill" (c) 1986,1993 by Udo Erasmus Ph.D. and published by Alive Books, Fraser Park Drive, Burnaby BC Canada V5J 5B9. On page 37 of this book at the top of the page it states that "Decreased metabolic rate is also involved in aging, arthritic diseases, cancer, and cardiovascular disorders, and is another general symptom of degenerative diseases." Published by Alive Books, 7436 Fraser Park Drive, Burnaby BC Canada V5J 5B9. (c) 1986,1993.
Exposure to cold temperatures will stimulate the production of TRH by means of dopaminergic neurons within the hypothalamus which stimulates the production of TSH by the pituitary which in turn stimulates the production of T4 by the thyroid which raises metabolism and body temperature to keep the body warm and to regulate the burning of fat and carbohydrates as fuel. The increased body temperature from a good metabolism stimulates the production of the anabolic hormone testosterone and anabolism keeps the body rejuvenated and fights aging. As I have shown interfering with this process lowers metabolism and shortens life span. Lowered metabolism causes weight gain and according to the American Medical Association's own statistics the more overweight a person is the more likely that person will suffer a premature death. See the chapter called "Drugs Used in Obesity" starting on page 2439 of the book "Drug Evaluations Annual 1995" by the American Medical Association. Neuroleptic drugs suppress the production of T4 thereby lowering metabolism by suppressing the release of the hypothalamic hormone TRH. Metabolism is the main mechanism that promotes thermogenesis. Thermogenesis is the production of body heat from the burning of fatty acids and glucose when body heat is lost due to exposure to cold temperatures and simply the continuous normal loss of body heat. It is T4 in the end that is responsible for helping to generate body heat that is lost and to keep the bodies metabolism going which includes both catabolism the burning of fat and glucose as fuel and anabolism the building up of the body through the maintenance and manufacture of replacement biochemical substances and structure which fights aging. Metabolism is both catabolic and anabolic. Although T4 technically is a catabolic hormone catabolism and anabolism are interconnected in a continues cycle so catabolism through T4 promotes anabolism. A healthy well nourished body will not burn protein as fuel.
Because of the neuroleptics or antipsychotics actions on the hypothalamus suppressing the release of TRH the pituitary doesn't produce as much TSH and in turn the Thyroid doesn't produce as much T4. See the book again "Facts and Comparisons". This book states under "Antipsychotic Agents" that neuroleptics "depress various components of the reticular activating system which is involved in the control of basal metabolic rate and body temperature, wakefulness, vasomotor tone, emesis, and hormonal balance." Also see the book "Cecil Textbook of Medicine 19th edition" edited by James B. Wyngaarden, MD, Lloyd H. Smith, Jr., MD and J. Claude Bennett, MD published by W.B. Saunders Company, Harcourt Brace Jovanovich, Inc. Philadelphia London, Toronto, Montreal, Sydney, Tokyo. This book states on page 1569 under "The Pathogenesis of Fever" under the subheading "Initiation of Fever" that "...thermoregulation originate[s] in the hypothalamus" and "... neuroleptic drugs are capable of disrupting the hypothalamic response and may interfere with the development of fever. Among these, [the neuroleptic] phenothiazines are the best known for their poikilothermic effect. These agents are not specifically active in febrile states; rather, they act to disable thermoregulatory mechanisms at all times following their administration." Also see the book called "AHFS 96 Drug Information" published by American Hospital Formulary Service and "published by the authority of the board of directors of the American Hospital Formulary Service. This book states on page 1617 at the bottom right of the page; "Phenothiazines have a poikilothermic effect, interfering with temperature regulation in the hypothalamus: depending on environmental conditions, hypothermia or hyperthermia can occur." Hypothermia is under heating of the body and hyperthermia is overheating of the body. Many people forced to take neuroleptics have died of heatstroke. See footnote A at the end of this thesis.
Again see the book "Drug Info for the Health Care Professional 17th edition volume I 1997" on page 2321 in the section on phenothiazines under the subheading "Mechanism of action/Effect" that neuroleptics "block postsynaptic mesolimbic dopaminergic receptors in the brain... and depress the release of hypothalamic and hypophyseal hormones." These effects are the result of blockage or destruction of dopamine receptors within the hypothalamus. Suppression of this hormonal system is one of the main mechanisms in which neuroleptics shorten life span.
Many of the quotes are obtained from statements concerning the class of neuroleptics called phenothiazines but since all neuroleptics block or destroy dopamine receptors they all produce the same undesirable symptoms. For instance this quote from the book "Drug Info for the Health Care Professional" page 1564 under the heading of "haloperidol" a neuroleptic in a class by its self; "[The] Pharmacological effects of haloperidol are similar to the effects of... phenothiazines". All neuroleptics block or destroy dopamine receptors so therefore all suppress hypothalamic hormone secretion. Now again see the book "Fats that Heal Fats that Kill" on page 37 at the top of the page where it states that "Decreased metabolic rate is also involved in aging, arthritic diseases, cancer, and cardiovascular disorders, and is another general symptom of degenerative disease." On page 191 of the same book at the top of the page it states; "The brightness of the fire is the rate at which our body produces energy our metabolic rate. For continued good health, it is vital that the fire of life burns brightly." Decreased metabolic rate not only leads to obesity but also to degenerative disease. Not only do neuroleptic drugs shorten life span but also make life inferior due to inducing the onset of degenerative disease.
See the book "Facts and Comparisons" again under "antipsychotic agents" and note that one of the neuroleptic drugs is sarcastically named "thioridazine" (Brand names are Mellaril, Novoridazine and Thioril) denoting the fact that these drugs suppress the production of the thyroid hormone thyroxine or T4. "Thio" being a grammatical construct from the beginning of the word thyroxine and also the beginning of the word iodine, which is the mineral that this hormone contains, followed by the word rid in the middle of this construct denoting the fact that these drugs get rid of or suppress the release of this hormone. In my opinion this reveals the utter contempt the designers of these drugs have for those labeled "mentally ill". Also the question must be asked, why would a drug be named after a life span shortening "side effect" unless that was its sole intended purpose? This also reveals that the designers of these drugs knew the biological effects of these drugs even before they were pushed on the public. Also notice that one of the neuroleptics is called "mesoridazine besylate" (Brand name is Serentil). Meso means middle which is where the limbic system is located in the brain. Since neuroleptic drugs shorten life span, the compulsory administration of these drugs by court order of the state is a violation of one's right to life.
Again see the book "Drug Info for the Health Care Professional 17th edition volume I 1997" on page 2321 which states that neuroleptics "block postsynaptic mesolimbic dopaminergic receptors in the brain ... [and] ... depress the release of hypothalamic and hypophyseal hormones." Again hypophyseal hormones are hormones produced by the pituitary gland. Because hypothalamic hormones control the release of pituitary hormones this is the reason pituitary hormones are suppressed. Most hypothalamic hormones are releasing hormones. One hypothalamic hormone which is an inhibiting hormone is prolactin release-inhibiting hormone (abbreviated PRIH also called PIF, RIH, prolactin inhibiting factor or prolactin inhibiting hormone, PIH, prolactostatin).
Since neuroleptic drugs suppress the release of this inhibiting hormone then the pituitary is free to secrete abnormal amounts of this female hormone that regulates lactation into the blood stream of both males and females. Most other bodily hormones are suppressed by neuroleptics except for prolactin for this reason. Since phenothiazines were the first neuroleptics used starting with Thorazine and the fact that phenothiazines have been used on more people then all other neuroleptics combined, the affect on hormone production caused by these drugs has been well established. All the other neuroleptics have been designed after what has been learned from the phenothiazines.
The level of hypothalamic hormone production is in direct correlation with dopaminergic activity or the ability of the dopaminergic system to function normally without interference. For this reason all neuroleptics that block or destroy dopamine receptors or utilize the serotoninergic system or both will suppress the production of all hypothalamic hormones which in turn suppresses pituitary hormone production and in turn all other bodily hormones.
Serotonin is an inhibiting neurotransmitter that mediates the function of the dopaminergic system. Excess serotonin stimulation has the effect of suppressing the dopaminergic system. One neuroleptic called Molindone (brand names Lidone and Moban) utilizes this function by mimicking serotonin. Also this is why antidepressant drugs that raise levels of serotonin cause sexual dysfunction. One "antidepressant" drug Sertraline (Brand name Zoloft) is molecularly indistinguishable from that of the neuroleptics. In fact Zoloft has even been tried as a neuroleptic. Perhaps it's labeled as an antidepressant just for people who insist that their "problems are just depression". A man I talked to on the telephone at the FDA told me that Zoloft was so powerful at destroying sexual function that if just one pill is taken by someone with premature ejaculation it will slow him down. But don't take this man's word for it. Even the PDR says Zoloft causes sexual dysfunction. Percentage rates of impotence listed in the PDR for various drugs is misleading as only people who were sexually active and not embarrassed to speak about it would even report impotence or sexual dysfunction as a side effect. Every male I have questioned who has been on these drugs has confided in me that these drugs have caused them some type of major sexual problem.
See the book "Biochemistry A Case-Oriented Approach fifth edition" by the Department of Biochemistry, The University of Iowa College of Medicine, Iowa City, Iowa. Montgomery Rex Ph.D., Thomas Conway Ph.D. and Arthur A. Spector MD (c) 1990 The C.V. Mosby Company. This book states on page 761 that prolactin secretion is increased by "serotonin". See the book "Facts and Comparisons" again under "antipsychotic agents" under "Carcinogenicity / prolactin secretion:" which states "Neuroleptic drugs elevate prolactin levels which persist during chronic administration." This is a reference to all neuroleptics, not just phenothiazines. Also see the book again called "Biochemistry A Case-Oriented Approach fifth edition" on page 761 in the seventh paragraph where it states that "Some medications, acting as dopamine antagonist, increase prolactin secretion. Although many drugs of this type exist, the most common are the antipsychotic phenothiazines, such as thorazine." On page 778 of this same book it states in the first paragraph; "Dopamine is an active compound believed to inhibit prolactin secretion".
Since neuroleptics block or destroy dopamine receptors there is no dopaminergic activity to inhibit prolactin secretion. Going back to page 761 of this same book it sates in the fifth paragraph under "Disorders associated with prolactin" that "Prolactin secretion has a dramatic effect in blocking the pituitary gonadotrophs, and elevated prolactin levels are associated with sexual dysfunction. Hyperprolactinemia before puberty blocks sexual maturation and the pubertal growth spurt. After puberty, hyperprolactinemia is associated with loss of libido and impotence in males and amenorrhea in females." The gonads are testicles in men and ovaries in women and amenorrea is the abnormal suspension or suppression of menstruation. Hyperprolactinemia is the abnormal excessive production of the female hormone prolactin.
One pituitary gonadotroph is luteinizing hormone (abbreviated LH and also called luteotrophin or luteotropin, interstitial cell-stimulating hormone, ICSH, Prolan B, gonadotrophin II or gonadotropin II, metakentrin, corpus luteum-ripening hormone). See the book again "Handbook of Vitamins, Minerals and Hormones" on page 323 under "Deficiency Diseases, Disorders" where it states that deficiency of this hormone causes "Hypogonadism". (Hypogonadism is the inability of the gonads to perform their function of remaining fertile and producing sex hormones.) Also on this page it states that this hormone is necessary for "reproduction". Now reference page 327 of this book under "Mode of Action" where it states that this hormone "increases synthesis of steroid hormones (sex hormones) ... estradiol (estrogen) ... [and] testosterone". Also here it also states that this hormone "stimulates rupture of follicles in ovary". (This is so the ova or egg can be released from the ovary.)
The other pituitary gonadotroph is follicle stimulating hormone (abbreviated FSH, and also called Follotropin or Follotrophin, Thylakentrin, Prolan A, gonadotrophin I or gonadotrophin I, gametogenic hormone, follicle ripening hormone, gametokinetic hormone). See the book again "Handbook of Vitamins, Minerals and Hormones" on page 330 where it states that this hormone is required for "reproduction". Also see page 332 under "Deficiency Symptoms" where it states that deficiency of this hormone causes "Decreased gametogenic function and development (nonfunctional)". (This is just a fancy way of saying that deficiency of this hormone will cause any sperm or ova produced to be genetically incapable of producing offspring or rendering any sperm or ova (eggs) produced "nonfunctional") Also on this page it states that deficiency of this hormone also causes "Atrophy of the gonads" (atrophy means to waste away), "No maturation of ova, sperm", "Obesity", "Decreased libido, potency, hair growth" and "decreased blood levels of estrogen". (Estrogen is the female sex hormone.) Pituitary gonadotrophs stimulate the production of sex hormones by the gonads.
The hypothalamic hormone, luteinizing hormone-releasing hormone regulates these pituitary gonadotrophs. (Abbreviated LRH also called LRF, LH-releasing factor or LH-releasing hormone, (LH-RH/FSH-RH), Gonadotropin releasing hormone (abbreviated Gon-RH or GnRH)) This hormone is suppressed by neuroleptics so here is another mechanism by which sex hormone production is inhibited besides the inhibition due to excessive prolactin secretion.
Going further on to the sex hormones which neuroleptic drugs inhibit we will learn more about what these drugs do to the body. Estradiol also called estrogen (some other names are female hormone, dihydrotheelin, dihydrofollicular hormone, dihydrofolliculin) "is essential for reproduction and female characteristics. Its chief functions are to maintain and regulate female sex characteristics and behavior. Its chief importance is as the major female sex hormone with its command of female sex development and maintenance of female body characteristics and behavior. ...Deficiency conditions include menopause and delayed maturation." As stated in the book "Hand Book of Vitamins, Minerals and Hormones" on page 415. (See footnote D) On page 419 of the book "Handbook of Vitamins, Minerals and Hormones" it states that deficiency of estrogen will cause "Delayed maturation", "Female accessory and reproductive organs recess" (recess means not to function), "Decreased female behavior pattern", "Senescence" (means Growing old, aging), and "Menopause". Here is further proof that neuroleptic drugs program the body to self-destruct, grow old and die and proof that these drugs prevent reproduction.
Another female hormone that is stimulated by the hypothalamic hormone, luteinizing hormone-releasing hormone through the pituitary hormone luteinizing hormone is progesterone. So therefore neuroleptics also inhibit the production of this hormone as well. On page 423 of the book "Handbook of Vitamins, Minerals and Hormones" it states that progesterone "is indirectly essential for life, since it is a precursor to aldosterone and cortisol, which is essential. Its chief functions are to synergize the actions of estradiol (estrogen) in the female organs, especially during pregnancy. Its importance stems from the fact that it is a precursor to all the steroid hormones and that estradiol (estrogen) requires its presence for many of its actions. ...Deficiency conditions [include]... dysfunctional uterine bleeding." On page 427 under "Deficiency Symptoms" this book states that deficiency of progesterone causes "Termination of pregnancy", "Decreased production of steroids", Decreased ovulation", "Loss of normal cyclic changes" and "Decreased development for implantation and gestation". This is shocking because neuroleptics are routinely given to pregnant women who commonly have miscarriages and then the prescribing psychiatrists will deny that the drugs were the cause!
Now onto the male sex hormone testosterone; Testosterone's "chief functions are: development and maintenance of the male organs, male sex characteristics, and behavior, as well as stimulation of growth (anabolic), and metabolism of muscles, liver; and kidney. The chief importance of testosterone lies in its major command of male sex development, body characteristics, and behavior. Deficiencies include eunuchoidism, and male hypogonadism. ...Testosterone is formed mainly in the testes (interstitial cells) but also in small amounts in the adrenal cortex and the ovary[s]." (From page 431 of the book "Handbook of Vitamins, Minerals and Hormones") On page 433 of this book it states that testosterone is "essential for reproduction in all (male) vertebrates". On page 435 of this book it states that deficiency of testosterone will cause, "Involution of accessory organs (prostate, seminal vesicles)", (involution is the progressive decline or degeneration of normal physiological functioning occurring as a result of the aging process and or decrease in size of an organ.) "Decreased male behavior patterns and libido", "Decreased secondary sex traits", "Poor muscle development and function". Neuroleptic drugs will destroy sexual function in men and produce sterility and will cause musculature to waste away since this is another hormone that neuroleptic drugs suppress the production of. See the web address below that states that risperidone (which is a neuroleptic in a class by itself) will cause "testicular atrophy" because of its "antidopaminergic activity". All neuroleptics though will cause testicular atrophy due to hormonal suppression. See "Atypical Antipsychotics: A Practical Review" at: Risperidone and do a search on the page for "testicular atrophy". You must first have a user name and password before accessing this article. It is open to anyone who wants a password.
I have received this
argument from someone who presented himself as a medical student. He said that
dopamine and Prolactin Release-Inhibiting Hormone is one and the same. He also
said "of course a drug acting as a dopamine antagonist is going to affect
this hormone". I had to set this man straight. I told him this: "That
is not true. Prolactin Release Inhibiting-Hormone (also known as PRIH,
Prolactostatin, RIH, Prolactin Inhibiting Factor or hormone, PIF, PIH, PRIF),
which is produced by the hypothalamus is a chain of amino acids similar in
structure to Luteinizing Hormone-Releasing Hormone. This can be found in the
book "The Handbook of Vitamins Minerals and Hormones" by Roman J.
Kutsky, Ph.D. on page 303, which is a very good biochemistry fact book written
in outline form. At the time of publication of this book the exact structure of
Prolactin Release-Inhibiting Hormone had not been determined but they knew
enough about it that they knew it was similar in structure to Luteinizing
Hormone-Releasing Hormone which is a chain of amino acids called a peptide which
is a small protein. Dopamine is a monoamine derived from the amino acids
L-Tyrosine and or L-Phenylalanine. It has been called "Prolactin Inhibiting
Factor" but should never be called "hormone" since it is a
neurotransmitter. Apparently there is much confusion in the medical field
regarding this. I also told this man this; "I can understand your confusion
because it has been known for years that Dopamine affected Prolactin, but by the
mechanisms pointed out in this report. Dopamine affects the release of all
hypothalamic hormones not just Prolactin Release Inhibiting Hormone or
Prolactostatin. Here is the exact amino acid sequence of PRIH; Asp - Ala - Glu -
Asn - Leu - Ile - Asp - Ser - Phe - Gln - Glu - Ile -Val - Lys - Glu - Val - Gly
- Gln - Leu - Ala - Glu - Thr - Gln - Arg - Phe - Glu - Cys - Thr - Thr - His -
Gln - Pro - Arg - Ser - Pro - Leu - Arg - Asp - Leu - Lys - Gly - Ala - Leu -
Glu - Ser - Leu - Ile - Glu - Glu - Glu - Thr - Gly - Gln - Lys - Lys - Ile".
I also told him this: "Dopamine is not a hormone but a neurotransmitter. No
doubt there are many independent neurological pathways that utilize this
stimulating neurotransmitter in the control of the release of these hypothalamic
hormones. That is why the release of these hormones operate independently of
each other and that dopamine antagonism inhibits all hypothalamic hormone
production because antagonism is not neurological pathway specific and never
will be. Which is why the drug chemical approach to treating "mental
illness" is fundamentally flawed and will never be the answer.
Go to this web-site where the hypothalamic peptide prolactostatin or prolactin release-inhibiting hormone is available for sale for research purposes. http://www.penlabs.com/biopro/biopeptides3_32.html It is called Prolactin Release Inhibiting Factor or (PIF) on this Web-site. Go here to this German language web-site where it is identified as a hypothalamic hormone. http://www-stud.uni-essen.de/~st0184/Infos/eseldiv.htm. The name Prolactostatin is used on this web-site. There are three hypothalamic "statins" and they are all inhibiting peptides. The idea that PRIH is dopamine is outmoded and erroneous. Dopamine is the controlling neurotransmitter involved in the release of PRIH. There have been studies in the past that seemed to suggest that dopamine acts directly on the pituitary to inhibit prolactin, but such studies are flawed in that infusing dopamine into the area of the pituitary to observe the affect on Prolactin release could very well be effecting real PRIH release from the hypothalamus simply because of the close proximity of the pituitary to the hypothalamus. The pituitary is after all at the base of the hypothalamus and this dopamine infusion could easily be crossing over into the hypothalamus and stimulating the dopaminergic system and therefore releasing real PRIH which in turn would inhibit prolactin thus giving the appearance that dopamine was the sole causative factor acting directly on the pituitary.
As has already been established neuroleptic drugs inhibit the production of the hormone progesterone and it is a precursor to the hormone aldosterone, (Precursor means the body uses one substance to synthesis or to produce another substance. In simpler words the body makes the hormone aldosterone from the hormone progesterone) so therefore aldosterone is also inhibited by neuroleptic drugs. See the book "Handbook of Vitamins, Minerals and Hormones" again on page 406 where many deficiency symptoms are cited which include "Muscular weakness" and "Stress intolerance". See the book again on page 401 where it states at the bottom of the page that aldosterone is "One of the most essential of all hormones; absence can be fatal in [a] short time period". Now look at the book "Facts and Comparisons" again under "antipsychotic agents" under "adverse reactions" where it states that after the administration of neuroleptics that "Sudden Death has occasionally been reported." Could this perhaps at least be partly due to the inhibition of aldosterone secretion by these neuroleptic drugs? Aldosterone secretion is partly governed by the pituitary hormone ACTH (the abbreviation for adrenocorticotropic hormone or adrenocorticotrophic hormone and also called adrenocorticotropin or adrenocorticotrophin, corticotropic hormone or corticotrophin hormone) which is in turn governed by release of the hypothalamic hormone corticotropin-releasing hormone or corticotrophin-releasing hormone. (Abbreviated CRH and also called CRF, cortical-releasing factor or cortical-releasing hormone, adrenocorticotropin-releasing factor or adrenocorticotrophin-releasing factor, corticotropin-releasing factor or corticotrophin-releasing factor.) See the book "Handbook of Vitamins Minerals and Hormones" again on page 342 at the bottom of the page where it states that ACTH is "one of the most essential hormones-Absence causes notable shortening of normal life span." Now see page 344 of this same book where it states that deficiency of ACTH causes "Decreased weight of adrenal (atrophy)", "Decreased mobilization of free fatty acids" (so fat can be burned as fuel). It also states here that deficiency of ACTH causes "Decreased steroids in blood, urine (17-hydroxy and 17-keto)" (ketones are produced as a byproduct of the burning of fat as fuel. Since deficiency of ACTH decreases ketones it means that fat is not being utilized as fuel which will lead to weight gain), "Fasting hypoglycemia" and "Increased insulin sensitivity" Which explains why it is common for people on these neuroleptic drugs to be glucose intolerant. Since neuroleptic drugs inhibit the production of all these hormones described above, they also cause all the problems associated with deficiency of these hormones. Here is unquestionable proof that neuroleptic drugs not only shorten life span but also destroy sexual function and fertility or the ability to procreate offspring or have children.
Aldosterone is not the only hormone that is controlled by the ACTH, CRH hormonal cascade. ACTH and CRH also control the release of the adrenal hormone cortisol (Also called hydrocortisone, Compound F, 17-hydroxycorticosterone. Substance M, glucocorticoid) (also cortisol is converted into cortisone in the body). On page 407 of the book "Handbook of Vitamins, Minerals and Hormones" it states that the "chief functions" of cortisol "are to maintain stress reactions, capillary permeability, release of other hormones, liver anabolism, and extrahepatic catabolism. Its chief importance is maintenance of stress reactions". ("liver anabolism" is the rejuvenation of the liver and liver synthesis of substances that keep the body rejuvenated and "extrahepatic catabolism" is the burning of fat as fuel in all parts of the body except for the liver.) Also on this page it states that "Factors inhibiting the release" of cortisol "are: high glucocorticoids, low ACTH, and pituitary hormones." On page 408 of this book it states at the bottom of the page that "Absence" of cortisol "causes shortening of life span due to inability to respond to stress situations." On page 411 of this book it states that deficiency of cortisol causes decreases in "Kidney function, leading to death", "Liver glycogen, gluconeogenesis", "Intestinal absorption, blood sugar" and "Stress response-Ultimately death". Also on page 411 it states that deficiency of cortisol will cause increases in "Fat anabolism, hemoconcentration" (Fat anabolism is the depositing of new fat tissue), "Muscular weakness" and others. Here is further proof that neuroleptic drugs shorten life span.
Now on to another hormone which neuroleptic drugs suppress the release of which is the pituitary hormone growth hormone. (Abbreviated GH and also called somatotropin or somatotrophin, phyone, anterior pituitary growth hormone, adenohypophyseal growth hormone, somatotrophic hormone, STH) You may think that this is not a problem because most of the people these drugs are given to are already adults or in their teens. (I have been recently discovering that a growing number of children with ADD or similar "conduct disorder" are being given these drugs.) But growth hormone has other functions in adults. See the book again called "Handbook of Vitamins, Minerals and Hormones" on page 307 where it states that "Because growth hormone controls the nitrogen balance of an organism, it is thought to be involved in the aging process." On page 309 of this same book it states that absence of growth hormone will result in a "decrease in normal life span." On page 311 it states that deficiency will result in "Increased fat deposition." The hypothalamic hormone growth hormone-releasing hormone (abbreviated GRH and also called GHRH, GRF, somatotropin-releasing factor or somatotrophin-releasing factor or somatotropin-releasing hormone or somatotrophin-releasing hormone, growth hormone releasing-releasing factor or growth hormone releasing-releasing hormone, SRF, GHRF) stimulates the secretion of growth hormone by the pituitary. As we have already learned neuroleptics suppress the release of both hypothalamic and pituitary hormones. Here is further evidence that neuroleptic drugs shorten life span. Therefore the compulsory administration of neuroleptic drugs by court order of the state is a violation of one's right to life.
Neuroleptic drugs also possess "adrenergic blocking effects". Again reference the book "Facts and Comparisons" under the section "Antipsychotic agents". The book states on the first page of this section "In addition, the drugs exert anticholinergic and alpha-adrenergic blocking effects." Also see the book "Drug Info for the Health Care Professional" again on page 2321 under the section on phenothiazines where it states under the subheading "Mechanism of action/effect" that "Phenothiazines also produce an alpha-adrenergic blocking effect." (Phenothiazines being just one of the classes of neuroleptic drugs all of which block dopamine receptors and cause the same effects due to blockage of these receptors.) This is so because of the chemical similarity of dopamine to the adrenergic neurotransmitters, all of which belong to a family of neurotransmitters called catecholamines. The adrenergic neurotransmitters are adrenaline and noradrenaline. (Also called epinephrine and norepinephrine) These two neurotransmitters are synthesized or created from dopamine; thus the similarity in their molecular structure. Both these neurotransmitters double as hormones. Since neuroleptics block or destroy alpha-adrenergic postsynaptic receptors this would simulate a deficiency.
See the book again "Handbook of Vitamins, Minerals and Hormones" this time under "Epinephrine". This book states on page 445 concerning epinephrine that "It is not essential for life, but it is indirectly essential, since it is involved in stress responses via cortisol, which is essential". (We have already learned the importance of cortisol.) On this same page it states that one of the functions of epinephrine or adrenaline is increasing metabolic rate in time of need to respond to stress or emergency. Also see page 447 under the subheading "Essentiality for Life" where it states that deficiency of this hormone and neurotransmitter will cause "possible shortening of life span due to decreased response to emergencies." So if threatened by a life threatening situation neuroleptic drugs make one physically ill equipped to face the threat. Also on page 448 under "Deficiency Symptoms", "Not fatal, but organism cannot respond to emergency, hard work, temperature extreme, emotional disturbance". Not fatal of course unless one fails to respond adequately to an emergency or dies of heatstroke. Again see the book "Facts and Comparisons" under "Antipsychotic Agents" under "Adverse Reactions" where it states that "Heatstroke/Hyperpyrexia induced by neuroleptics has occurred. They may act in several ways including disrupting the hypothalamic thermoregulator center, alpha-adrenergic blockage and autonomic mechanisms." (Hyperpyrexia is overheating of the body.) And of course not being able to respond to emotional disturbance or stress blocking the stress response making one incapable of dealing with stress thus precipitating agitation. This is destructive to the body in it's own right so here is another way these neuroleptic drugs shorten life span. Also appetite is controlled in part by noradrenaline within the hypothalamus. Lowered metabolism and the compulsion to consume more food due to increased appetite from the blockage of noradrenaline receptors within the hypothalamus equals weight gain. It can not be avoided. See the book again called "Facts and Comparisons" under "antipsychotic agents" under "Adverse Reactions" under "Miscellaneous" which states that neuroleptics will cause "increases in appetite and weight".
Neuroleptics also have "anticholinergic blocking effects". Acetylcholine is a neurotransmitter. The brain produces an enzyme called acetylcholinesterase to break down excess acetylcholine to prevent it from accumulating to abnormal levels. This break down of acetylcholine by this enzyme comprises the anticholinergic system. Neuroleptic drugs have "anticholinergic blocking effects" meaning they cause the accumulation of acetylcholine to abnormal levels. Nerve gas's method of causing death is by its anticholinergic blocking activity. Also insecticide kills insects by this same method causing an abnormal build up of acetylcholine in the brain and nervous system of the insect.
See the book again called "Facts and Comparisons" under "antipsychotic agents" at the bottom of the first page in this section where it states that "In addition, the drugs exert anticholinergic and alpha-adrenergic blocking effects." Now see the book called "Brainscapes" by Richard M. Restak, MD published by NY Herperion (c) 1995. On page 57 of this book it states; "As we have discussed earlier, after a neurotransmitter and it's receptor have reacted, the process must be brought to a halt, which is accomplished either by the destruction of the neurotransmitter and recycling of it's constituents, or by a so-called reuptake system, whereby the neurotransmitter is recaptured and stored once again within the vesicle. In the case of acetylcholine, the process involves a breakdown brought about by the enzyme acetylcholinesterase, which cleaves the neurotransmitter back to its original chemical building blocks. This process can be interfered with by compounds responsible for some of the worst horrors of twentieth-century warfare. Nerve gases, such as the deadly Sarin released into the subway system in Tokyo in March 1995, form irreversible bonds with anticholinesterase [acetylcholinesterase], thus inhibiting the enzymes' ability to break down acetylcholine in the synapse." Then on page 121 of this same book it states; "In the section on neurotransmitters we mentioned another class of neurotoxins, inhibitors of the enzyme acetylcholinesterase, which breaks down the neurotransmitter acetylcholine. Many pesticides are designed to attack the nervous system of insects by altering the breakdown of acetylcholine. Not surprisingly, these agents also act on our brains and nervous systems to produce symptoms like weakness, difficulty in breathing, visual disturbances, and in some cases explosive violence. With low rates of exposure the problems are more subtle, a prevailing sense of tension, disturbed sleep, restlessness, chronic anxiety, and nervousness when standing in lines."
All of these symptoms can be observed in people on neuroleptics. For instance "visual disturbances", see the book again "Facts and Comparisons" under "Ocular" in Adverse Reactions which states that neuroleptics will cause "Glaucoma; photophobia; blurred vision; miosis; mydriasis; ptosis; star-shaped lenticular opacities; epithelial keratopathies; pigmentary retinopathy. Eye lesions may regress after drug withdrawal." Also as Richard Restak MD reports insecticide exposure will cause "restlessness" and or "nervousness when standing in lines." This has been given a name "Akathisia", see the book again "Facts and Comparisons" under "Extrapyramidal" under "akathisia" which states that neuroleptics cause "a condition of constant motor restlessness [called akathisia] and may include feelings of muscle quivering, an inability to sit still and an urge to constantly move about." Akathisia comes from the Greek word meaning "can't sit still," and refers to significant physical and mental agitation. Akathisia is to violence what a match is to gasoline. Also he reports that insecticide exposure will cause "difficulty breathing", again see the book "Facts and Comparisons" in the same section under "Respiratory" which states that neuroleptics cause "Laryngospasm; bronchospasm; increased depth of respiration; dyspnea." (Dyspnea is difficulty breathing or shortness of breath.) Also he states that insecticide exposure will cause "weakness", again see the book "Facts and Comparisons" in the same section under "Other CNS effects:" that neuroleptic drugs will cause "Cerebral edema, headache, weakness, tremor, staggering gait; twitching; tension; jitteriness; akinesia; ataxia; fatigue; slurring [of speech]; abnormal cerebrospinal fluid proteins;" etc. Also Richard Restak MD reports that insecticide exposure will cause "disturbed sleep". Again see the book "Facts and Comparisons" in the same section under "Other CNS effects" where it states that these drugs cause "insomnia" and under "Adverse behavioral effects:" where it states that neuroleptic drugs cause "nocturnal confusion" and "bizarre dreams". Richard Restak MD also reports that insecticide exposure will cause "a prevailing sense of tension", again see the book "Facts and Comparisons" under "Other CNS effects" where it states that neuroleptics cause "tension". Also he reports that insecticide exposure will cause "anxiety". Now see the book called "The Essential Guide to Prescription Drugs Revised Edition" (c) 1980 by James W. Long MD and published by Harper & Row on page 344 under haloperadol (a neuroleptic drug) that this drug can cause "anxiety". Also Richard Restak MD reports in his book that insecticide exposure causes "in some cases, explosive violence." Now see the book "Facts and Comparisons" in the same section under "Adverse behavioral effects:" where it states that neuroleptics can cause "hyperactivity" and "agitation". (See the commentary coming up concerning a Star Trek Voyager episode entitled "The Chute" where the story centered on this very effect.)
Of course nerve gas and insecticide are poisons and neuroleptics have blatantly poisonous properties in that part of their function is the same as that of nerve gas and insecticide in causing an abnormal build up of acetylcholine. In fact the very molecular base of one class of neuroleptics called phenothiazines is used as an insecticide! See the book again entitled "AHFS 96 Drug Information American Hospital Formulary Service" in the second paragraph in the right column, which states that "Phenothiazine [a class of neuroleptics] is still used as an anthelmintic in veterinary medicine and as an insecticide." The very insecticides that Richard Restak MD is referring to in his book "Brainscapes" are being given to those labeled mentally ill as a claimed "beneficial medical treatment"! Here is further evidence that neuroleptics shorten life span. Again remember that all neuroleptics interfere with the breakdown of acetylcholine so don't assume that because the drug isn't a phenothiazine that it will not have these effects. Other neuroleptics may even be worse at interfering with the break down of acetylcholine then phenothiazine.
Personally every time I have been on neuroleptics I have been extremely agitated sometimes breaking things. One time I even assaulted my father because of these drugs. These drugs can cause extreme feelings of rage. This is precipitated by the horrible torturous feelings that these drugs induce. This well-known effect of excess acetylcholine was even the theme for a Star Trek Voyager episode called "The Chute" (this is an American science fiction television show) in which two of the members of the crew were abducted and placed aboard a space station prison. In order to keep the prison population down the prisoners where unknowingly exposed to a chemical that caused the build up of acetylcholine by interfering with its breakdown. This caused the prisoners to be violent and enraged often killing each other. After the crew members were rescued the "holographic" doctor on Voyager revealed that it was interference with the breakdown of acetylcholine that was causing the violence and that the prison's operators must be using the chemical to keep the prison’s population down. (Could this be why many prisoners in the USA are forced or coerced into taking neuroleptic drugs?) Based on this fact of neuroleptics, not only is compulsory administration of neuroleptic drugs by court order of the state a violation of the right to life but also the pursuit of happiness because these drugs take away one's sense of well being causing "agitation". Ironically these drugs are often prescribed under the pretense that they will prevent violence when in reality they can actually promote it.
This leads to another problem with neuroleptic drugs and how they take away sense of well being. Within the limbic system of the brain is an electrochemical cascade called the "reward system". This system is responsible for giving a person their sense of well being. Disruption of this electrochemical neuronal cascade results in ones sense of well being, being supplanted with negative emotions such as anxiety, depression, anger and generally a very negative outlook on things. The end result of the reward system's neuronal cascade is stimulation of dopamine D2 receptors within the nucleus accumbens and the hippocampus, which are located within the limbic system of the brain.
See a problem yet? Remember neuroleptic drugs as you have already learned block or destroy dopamine D2 receptors preventing their stimulation by the neurotransmitter dopamine. Again see the book "Facts and Comparisons" under "Antipsychotic Agents" where it states on the first page of this section; "Antipsychotics block postsynaptic dopamine receptors in the basal ganglia, hypothalamus, limbic system, brain stem and medulla. ...The phenothiazines appear to act at both D1 and D2 receptors, whereas haloperadol appears to act primarily at D2 receptors."
Neuroleptics do indeed take away one's sense of well being by utilizing more then one mechanism. This is very self destructive to the body and will result in a premature death if one doesn't commit suicide first. Ironically these drugs are prescribed to people to prevent suicide when in reality they actually promote it. Perhaps the designers of these drugs want to give the person that extra amount to push them over the edge and actually do it. Personally two times I was on these drugs for extended periods I attempted suicide because of them.
So here is further proof that the compulsory administration of neuroleptic drugs because of court order of the state is not only a violation of one's right to life but also one's right to the pursuit of happiness. This is so since the administration of these drugs take away sense of well being making it very difficult to feel happiness.
Read the article entitled "Reward Deficiency Syndrome" as published in "American Scientist" magazine March-April 1996 for a detailed and in depth discussion of this brain function called the "reward cascade". Click Here for Article Online. This magazine article states on page 135 under figure 4, "If the activity of the dopamine D2 receptor is deficient, the activity of neurons in the nucleus accumbens and the hippocampus is decreased, and the individual experiences unpleasant emotions or cravings for substances that can provide temporary relief by releasing dopamine." On page 132 of this article it states that disruption of the stimulation of D2 receptors as part of the "reward cascade" will "supplant an individual's feeling of well being with anxiety, anger or a craving for a substance that can alleviate the negative emotions." In this magazine article it explains that "reward deficiency syndrome" is the cause of behavioral disorders such as attention deficit disorder (with and without hyperactivity), personality disorder, conduct disorder, antisocial personality, aggressive behavior, autism (autism is the abnormal introversion and egocentricity, acceptance of fantasy rather then reality).
After reading this article I came to understand the source of many of my own problems and why neuroleptics were exasperating them. And also why I had an insatiable craving for alcohol whenever I was on neuroleptics that even persisted for a long time after they were discontinued since the damage caused by neuroleptics to the dopaminergic system is long term. Or I would consume caffeinated cola flavored soda - craving the caffeine - until my stomach would become bloated and I would throw up. Again see the book "Facts and Comparisons" under "antipsychotic agents" under "Adverse Reactions" under "Adverse behavioral effects:" where it states that neuroleptics will cause "...restlessness; hyperactivity; agitation; ... depression; ... paranoid reactions." And again see the book "The Essential Guide to Prescription Drugs Revised Edition" (c) 1980 where it states that haloperadol (a neuroleptic) causes "anxiety". Also as reported in this report, since these neuroleptic drugs cause adrenergic blocking and inhibition of the adrenal hormone cortisol, these drugs reduce capacity to deal with stress both emotionally and physically. So here is irrefutable proof that these drugs not only take away sense of well being but also shorten life span.
The state does NOT have the right under any circumstances to order the compulsory administration of a substance, which shortens life span and takes away one's sense of well being, a substance with poisonous properties like that of nerve gas and insecticide! The constitution of the United States of America guarantees certain inalienable rights, namely the right to liberty (making one’s own decision regarding personal matters), the right to life, and the right to the pursuit of happiness. When the state orders the compulsory administration of neuroleptics EVERY ONE of these inalienable rights is being violated.
Mental health officials will first do their very best to intimidate and coerce a "patient" or "client" into "voluntarily" taking neuroleptics before they will attempt to get a court order that will allow them to involuntarily drug someone. They will use mind games or psychology on a person coming back to them repeatedly telling them such things as "Don’t you want to get better?". Many times when doing this they will invade your personal space. Perhaps in an attempt to provoke you into an act of violence that they will then use as "evidence" that you "need" these drugs. Many times they will tell the person that they will not qualify for social security assistance if they do not take the drugs or that they will remain locked up in an institution if they do not take the drugs. Any call to the Social Security Administration will reveal that it is not required that someone takes neuroleptics in order to receive or continue to receive social security. Perhaps what the psychiatrists are really saying is that they will not support a disability claim if the person doesn't take the drugs. In such case this is blackmail. Don't be tricked by a psychiatrist's attempts to get you to try a new drug that is supposed to be "safer" then the older ones. All neuroleptics block or destroy dopamine receptors even the newer ones. Therefore the newer so called, "safer" neuroleptics will also cause what has been described in this report by the very fact that they also block or destroy dopamine receptors. Risperidone (Brand name Risperdal) and Zyprexa (Brand name is Olanzapine) affect higher reasoning centers and make it almost impossible to form complex thoughts. This is due to its effects on the neurotransmitter Serotonin. If I were on either of these two drugs it would have been impossible for me to do the research and write this report. I speak form experience because I have temporarily taken both Zyprexa and Risperidone. On just two pills of Zyprexa I could not even access my memories of research on these drugs. On Risperidone I had slurred speech, word substitutions, difficulty forming complex thoughts pages of text appeared as blank piece of paper when previously I could rapidly digest the material.
Resist psychiatric drugging. Use the evidence in this report to argue in probate court that the involuntary administration of these drugs is a violation of all your fundamental constitutional rights, most importantly the right to life and the pursuit of happiness. They will not be able to get around these two rights. They take away liberty from the "mentally ill" under the guise that they are supposedly not competent to make their own decisions regarding their own medical care, but they will not be able to get around these other two rights. If possible get your own attorney rather then allowing the court to appoint one for you because it is my experience that these court appointed attorneys are not really motivated to defend you and may even be secretly serving the interest of the mental health officials and the state. If you do not get a favorable decision in the probate court then insist on an appeal and remember to attempt to maintain your determination to follow through with the appeal realizing that these drugs take away your will power and ability to resist domination. Use this knowledge to fight this effect of the drugs. If necessary appeal these constitutional issues all the way to the Supreme Court. Only when we as a people fight and defend our rights will changes be made, not only for our personal protection but also for that of our loved ones and our children and our children's children. It is not just the "mentally ill" that are affected by this. Routinely these drugs are administered to the retarded (including children) and the elderly in nursing homes as well as Alzheimer's patients, people with head injuries or brain damage etc.
It is very clear that the motivation behind the administration of antipsychotics, antipsychotic drugs, neuroleptics, or neuroleptic drugs to the "mentally ill" and others is eugenic in nature. For those who do not know what eugenics is, it is idea that the human race can be improved by preventing "inferior stock" from reproducing and by inducing an early death. The eugenic idea got its start with psychiatrists in the USA. Later Hitler shocked the world with the holocaust of millions of people, basing his program on eugenics practices that were already being carried out in the USA. But the first to be killed in Nazi Germany was the "mentally ill". Before Hitler did the things he did, the forced sterilization of the "mentally ill" in the USA was common practice. But as you are already probably starting to see after reading the evidence centered on neuroleptic drugs, the same eugenics program is being covertly carried out under the guise of a "beneficial medical treatment". In the 1960s, the Eugenics Society of England adopted what they called "Crypto-eugenics", stating in their official reports that they would do eugenics through means and instruments not labeled as eugenics. Abortion and the push of birth control is one of these and as it should be clear from reading this report on the true nature of neuroleptic drugs that it is a eugenics conspiracy also.
After World War II so many psychiatrists immigrated to the USA that some time after the war, one third of all psychiatrists in the USA were former Nazi's.
The following excerpt is taken from the public service publication entitled "Psychiatry Destroying Religion in the Name of Salvation" by the Citizens Commission on Human Rights under the chapter entitled "The Devil's Doctors - From the Nazi Holocaust to 'Assisted Suicide'"
"While psychiatry has tried to expunge any connection between itself and the racial genocide of the Nazi Holocaust, the hard facts is that psychiatry spawned "eugenics" almost three decades before the Nazi's took power in 1933. It was psychiatry that turned the Nazis into the mass murders, not vice versa. And it was their ideology which fired Hitler's mania to eradicate religion."
"As early as 1895, German psychiatrist Alfred Ploetz wrote: "Should it turn out that in spite of it the new-born is a weakly and ill-bread child, then a gentle death will be provided for him by the medical board, which decides over the citizenship papers of the society, let's say through a small dose of morphine.... [The parents] will not give themselves over to rebellious feelings for long but will try it fresh and happily a second time, if they are permitted to do so and have a certificate granting them the right to the procedure."" [Dr. Thomas Roder and Volker Kubillus, Manner hinter Hitler (Malters: p Pi-Verlag fur Politik und Gesellschaft, 1994) pp. 65-66]
"Within ten years, Ploetz founded the German Society for Racial Hygiene, joining with another psychiatrist, Ernst Rudin who would later turn sterilization operations into one of the Nazi's most prolific death machines. Declaring racial hygiene a "spiritual movement," Rudin and his associates worked to disseminate their ideas and principles to the public. Despite "quietly and gradually winning over the hearts and minds of our best Germans," they could not gain support at upper government levels. Eventually they found a willing collaborator in Adolf Hitler. "Only through [the Fuhrer] did our dream of over thirty years, that of applying racial hygiene to society, become a reality,"" Rudin said. [Dr. Thomas Ruder, Volker Kubillus and Anthony Burwell, Psychiatrist the Men Behind Hitler (Los Angeles: Freedom Publishing, 1995) p. 94.]
"Hitler was also influenced by two psychiatric books: The Release of the Destruction of Life Devoid of Value (1920) by Hoche and Binding and The Principles of Human Heredity and Racial Hygiene (1921) by Bauer, Fischer and Lentz. Lentz wrote, "I have heard that Hitler had read the second edition of Bauer-Fischer-Lentz during his incarceration in Landsberg. Some parts of it are mirrored in Hitler's phrases. In any case, with great mental energy, he had made the basic ideas of racial hygiene and their importance his own, while most of the academic authorities still look upon these issues rather unappreciatively." [Roder, Kubillus, and Burwell, op. Cit., p. 37.]
"According to Hoche and Binding:
1. The suffering of a sick or wounded person who is about to die can be shortened through the use of a medical drug.
2. The acceleration of the death process is not an act of murder but "in truth a pure act of healing."
3. A doctor should be allowed to employ euthanasia on any unconscious person without legal consequences.
4. There are people who are worthless to society. Primary among these are the inmates of the "idiot institutions," who are "not only worthless, but of absolutely negative value."
5. The incurably dumb who can neither agree to survive or to be killed should be killed. "Their death will not be missed in the least except maybe in the hearts of their mother or guardian.... When we become more advanced, we will probably be saving those poor humans from themselves."" [Ibid., p.41.]
"With Hitler providing the public face and vehicle for implementation, the next few years saw an avalanche of legislation which legitimized psychiatry's demonic plans. On July 4, 1933, the Sterilization Act was enacted, clearing the path for wholesale euthanasia. July 4, 1933 saw the Law for the Prevention of Genetically Diseased Children passed."
"By 1936, the first systematic transfers of the mentally ill from various institutions to the concentration camps began. In 1937, criminals and repeat offenders were relocated to the camps, followed by "vagrants, alcoholics, work dodgers, welfare recipients and even already-sterilized, feeble minded women." That same year, the Third Reich embarked upon a cleansing of the churches and charitable establishments. People were relocated first into state institutions, then ultimately to the death camps."
"The number of sterilizations performed in Germany between 1934 and 1945 is estimated to be as high as 350,000. And while German psychiatric hospitals held 300,000 to 320,000 patients in 1939, only 40,000 were alive in 1946. The rest had met their deaths at the hands of psychiatry. [Ibid., p. 48; Fredric Wertham, M.D., A Sign For Cain: An Exploration of Human Violence (London: Robert Hale Limited, 1966), p. 158.] In 1941, the Hadamar psychiatric institution "celebrated the cremation of the ten thousandth mental patient in a special ceremony. Psychiatrists, nurses, attendants, and secretaries all participated. Everybody received a bottle of beer for the occasion," author Fredric Wertham, M.D. reported." [Wertham, A Sign For Cain..., op. Cit., p. 157.]
End of excerpt from the public service publication entitled "Psychiatry Destroying Religion in the Name of Salvation" by the Citizens Commission on Human Rights under the chapter entitled "The Devil's Doctors - From the Nazi Holocaust to 'Assisted Suicide.'"
The Citizens Commission on Human Rights is a non-profit anti-psychiatry organization that works hard to expose psychiatry for what it is. They offer many public service publications free of charge. But I recommend a small donation so they can keep up their very important work. Their address is: Citizens Commission on Human Rights International, 6362 Hollywood Boulevard, Suite B, Los Angeles, CA 90028. Their telephone numbers are 1-800-869-2247 or 213-467-4242. Their web-address is: http://www.cchr.org Although this organization is run by the Church of Scientology their anti-psychiatry public service literature doesn't teach Scientology. My quote from them above should not be construed as my endorsement of Scientology as I am not a Scientologist nor am I familiar with what they teach.
Also another organization to get in contact with is Support Coalition International a group calling themselves "psychiatric survivors" at the web address http://www.mindfreedom.org See this web-site on psychiatric drugs: http://www.antipsychiatry.org/drugs.htm . Also go here. http://www.wildestcolts.com Discusses electroconvulsive "therapy". This Internet resource called Psychiatric Tattler contains information worth reading. http://www.ect.org/tattler and a links page to other fine sites here: http://www.ect.org/tattler/links.html. Also see these anti-psychiatry links on this web-site: http://www.psychnet-uk.com/psychiatry/antipsychiatry.htm. Also see the links at: http://www.mentalhealthfacts.com/mhresources.html and http://www.schizoaffective.org and http://www.mentalhealthfacts.com .
It is very clear that psychiatry kills. The term psychiatric abuse is an understatement because the whole purpose of psychiatry is to abuse. The only legitimate form of psychiatry is that of the talking psychiatrist who doesn't use mind altering chemicals. This is the type of psychiatrist Dr. Peter R. Breggin, M.D. author of Toxic Psychiatry is. God bless Dr. Peter Breggin MD for his work. If you haven't already, read his book entitled Toxic Psychiatry for a lot of good info. This is Dr. Peter Breggin’s web-site address. http://www.breggin.com Psychiatry kills.
The thesis above concerning the biological ramifications of the administration of these drugs is new and is not contained in Dr. Peter Breggin's book but his book does contain a great deal of useful information not contained in this report.
Resist psychiatry’s forced drugging. Use the evidence in this report to argue in probate court that the involuntary administration of these drugs is a violation of all your fundamental constitutional rights, most importantly the right to life and the pursuit of happiness. They will not be able to get around these two rights. They take away liberty from the "mentally ill" under the guise that they are supposedly not competent to make their own decisions regarding their own medical care, but they will not be able to get around these other two rights. If possible get your own attorney rather then allowing the court to appoint one for you because it is my experience that these court appointed attorneys are not really motivated to defend you and may even be secretly serving the interest of the other side. If you do not get a favorable decision in the probate court then insist on an appeal and remember to attempt to maintain your determination to follow through with the appeal realizing that these drugs take away your will power and ability to resist domination. Use this knowledge to fight this effect of the drugs. If necessary appeal these constitutional issues all the way to the Supreme Court. Only when we as a people fight and defend our rights will changes be made, not only for our personal protection but also for that of our loved ones and our children and our children's children.
You can beat psychiatric drugging. If you resist they will more then likely back down. It costs a lot of money to house someone in an institution and the county you live in must pay for it. In Ohio medicaid pays $480 a day and the state picks up the rest for a total cost of $800 to $1000 a day. Nine times out of ten they will be unwilling to do this, so stick by your guns and resist psychiatric drugging. Don’t show up to get the injections and make them send a police officer after you to bring you into the inpatient unit. All this resistance will pay off because they will more then likely give up. They will lock you up in isolation for a few days hoping they will be able to brake your will power. If you continue to resist and maintain your resolve they will give up. Believe me, I speak from experience. If they do send you to an institution then 9 times out of 10 this will be a scare tactic and will only be temporary so maintain your resolve to resist. Be sure to never sign anything they want you to sign no matter what. If they apply a lot of pressure to get you to sign something just say that you want your lawyer to read it first. They keep people up to 90 days by court order in an institution so stick by your guns on the rare chance that this happens to you. Use the evidence in this report to fight for your rights in court and appeal if necessary all the way to the USA Supreme Court. Also remember to not fight back in any physical way even under extreme provocation because they will take this as proof that they are justified in any action they take against you and will be detrimental in any defense you may offer to the court. Use passive resistance. Make them hold you down to give you injections but do not try to harm the provocateurs.
You can also protect yourself by getting a living will, which states your wishes should you ever become "incompetent". If you are currently involved in the mental health system it will become necessary to have your lawyer accompany you to see your psychiatrist, psychologist, counselor, therapist etc. to get them to sign an affidavit concerning your current competency to enter into a living will. Don’t tell the mental health official that you want this affidavit for the purpose of avoiding involuntary drugging or you will most likely not get their cooperation. Tell them that you need a living will so you will not be kept on life support should you become brain dead etc. so they will be likely to cooperate. You will need this affidavit as a technicality so it can not be claimed at a later date that because you were involved in the mental health system that at the time you entered into the living will you were not competent to do so.
It is not just the "mentally ill" that are affected by this. Routinely these drugs are administered to the retarded (including children) and the elderly in nursing homes as well as Alzheimer's patients, people with head injuries or brain damage etc... These drugs are even prescribed to teenagers and young children who simply have a hot temper, which ironically the drugs make worse.
To biochemist, biologist, nutritionist, physicians, etc. If you have additional information and or references to add to the material presented below then please contact me at one of the E-mail addresses provided or contact the mailing address provided. It would be greatly appreciated. Also if any psychiatrists, psychologists, FDA or pharmaceutical officials or employees etc. that want to turn whistle blower by adding more information to what is provided in this report or by providing proof that a conspiracy is involved concerning these drugs then please E-mail one of the E-mail addresses or the mailing address provided below. Words can not express how much it would be appreciated. Your identity will be held in the strictest of confidence if you so desire.
IMPORTANT! Save this document while you have it because it is actively being censored. Please aggressively disseminate this information. E-mail, fax or mail this report to senators, congressmen and others involved in the government and politics. Also give a copy to your family doctor because many doctors are ignorant of the facts or have never considered the ramifications. E-mail, fax or mail this report to probate judges, appeal judges, and others involved in the government and politics. E-mail, fax or mail it to lawyers, civil and human rights organizations. E-mail, fax or mail this report to the media. Give a copy to local law enforcement officials. Give copies to neighbors, family, friends, people at work, and mental health patients and their family. Post this report on wwwboards and the news groups all over the Internet, not only in the USA but also in other countries. Please post it to the web and get others to link to it. Pass it along by direct E-mail to others on the Internet. It is very important that this information be disseminated to everyone. You can only protect yourself, friends, family and other loved ones through knowledge and knowledge is power. PLEASE disseminate this information aggressively so changes can be made in current law in many states. And please keep this entire report complete and intact when doing so.
List of neuroleptic drug names: chlorpromazine, (Brand names are as follows; chlor-PZ, klorazine, promachlor, promapar, sonazine, thorazine, chlorprom, chlor-promanyl and largactil) fluphenazine, (Brand names are as follows; permitil, prolixin, modecate, moditen) mesoridazine besylate, (Brand name is serentil) perphenazine, (Brand names are as follows; trilafon, etrafon, triavil, phenazine and etrafon) prochlorperazine, (Brand names are as follows; compazine and stemetil) promazine hydrocloride, (Brand name sparine) thioridazine, (Brand names are mellaril, novoridazine and thioril) trifuoperazine, (Brand names are as follows; stelazine, clinazine, novaflurazine, pentazine, terfluzine and triflurin) clozapine, (Brand named clozaril in Germany called leponex) haloperadol, (Brand name haldol) loxapine, (Brand name loxitane) pimozide (Brand name is orap) thiothixene, (Brand name navane) risperidone (Brand name risperdal), zyprexa (Brand name is olanzapine), sertindole, ziprasidone, (Brand name geodon or geodone. Was planned to be named zeldox) amperozide, remoxipride, melperone, zotepine, isofloxythepin, setoperone, perospirone, quetiapine (Brand name seroquel) methotrimeprazine (Brand name nozinan or nosinan, called levomepromazin in Germany), zuclopenthixol (Brand name clopixol ), zuclopenthixol acetate (Brand name clopixol acuphase), amisulpride (Brand name solian). Also the antidepressant drug sertraline (Brand name zoloft) is molecularly indistinguishable from that of the neuroleptics and has even been tried as a neuroleptic. This list contains generic names and many brand names used in the USA and Canada. This list is by no means comprehensive. Please help provide the names used in other countries by E-mailing me.
All the drugs above affect metabolism and the production of hormones in the body by their dopamine antagonism. All these drugs will shorten life span by their very nature and the FDA does not even require animal test on these drugs to determine how they affect the duration of life span. Such test should be done with guinea pigs because of their inability to manufacture their own vitamin C within their livers like that of us humans. Psychiatry is abusive and the whips and chains of Bedlam live on but they are now chemical in nature.
If you have additional information to add then please E-mail me. Or write to me at Sam Moser, 5700 Mallard Dr. Huber Heights OH 45424 USA
Footnote A: Support Coalition International reported: Consider the well-publicized heat wave deaths in the summer of '95. Member Jerry Egan sent Dendron the Chicago Tribune (7/22 & 7/26/95) in which Medical Examiner Jeffrey Jentzen revealed that "in Milwaukee, 15 of the 24 deaths due to heat stroke also involved psychiatric drugs." In other words, the coroner attributed more than 60% of these deaths to psychiatric drugs. According to the US Dept. of Health & Human Services, neuroleptics are indeed a major culprit in heat wave deaths (DHHS MMWR; 6/30/95, p. 467) Dr. Frederick Zugibe, medical examiner of Rockland County in New York State, is a hero in our movement for breaking the silence over these past 20 years about neuroleptic-related deaths. In a phone interview, he recalled how his autopsy findings about frequent neuroleptic-related deaths made the front page of The New York Times [7/17/78]. Whistleblowing led to harassment. "Colleagues even called me late at night saying I should resign," said Zugibe, "but I stayed at my job, and later I won awards." Little has changed he said, and he partly blames coroners for remaining so silent.
Footnote B: An inspection of the molecular structure of most neuroleptics will reveal reactive compounds molecularly bounded to the benzene ring of these drugs such as fluorine and chlorine. It is these reactive compounds that give the molecule its catalytic ability to destroy the receptor by cleaving the protein apart that makes up the receptor. Both the neuroleptics that act on dopamine receptors (as well as other psychoactive drugs) and the neurotransmitter dopamine and other catecholamines contain a benzene ring. This is the mechanism that most neuroleptics employ in destroying the receptors, which are on the ends of dendrites. So as you can see the function of these drugs is to create damage to the dopaminergic system. In effect the drugs cause brain damage. Dr. Peter Breggin reveals in his book "Toxic Psychiatry" studies that have been done that reveal people who have been on these drugs for ten years or more have a severely atrophied brain (brain shrinkage). People in their thirties who have been on these drugs for ten years or more have the brain size of a person in their seventies. Since these drugs destroy or disable the dopaminergic receptors they prevent dopamine from interacting with the receptor ever again forcing neurons to randomly grow new dendrites creating neurofibrillary tangles in a defensive measure to counteract the brain damage. After a person goes off the drugs in time new receptors will form but the brain changes caused by the drugs are permanent. Personally I suffered problems with hyperpyrexia two years after I received two 100mg Haldol dec injections and still have a very low tolerance to high temperatures. I have a theory that the brain shrinkage caused by these drugs is at least partly due to fact that the brain is constantly attempting to replace lost receptors and amino acids are constantly being used to construct new receptors taking away from the amino acid needs of other brain systems leading to the atrophy. Studies have also shown that phenothiazine promote the production of free radicals in the brain and body. (Chignell, C.F., Motten, A.G. and Buettner, G.R. (1985) "Photoinduced free radicals from chlorpromazine and related phenothiazines. Relationship to phenothiazine induced photosensitization." Environ. Health Perspect., 64, 103 110.) Free radicals are believed to be one of the causes of the neurofibrillary tangles found in Alzheimer's patients and also the brain damage of Parkinson's Disease. Ironically these drugs are commonly given to patients with Alzheimer's Disease which these drugs make worse. Also free radicals are believed to be a major cause in the aging process. Here is more proof psychiatric drugs shorten life span.
Footnote C: A legitimate religious ground for not taking these drugs would be the Christian Biblical teaching that the use of mind altering chemicals and poisons on someone is witchcraft. Witches used to exercise their control over others through a "magick spell" using secret mind altering chemicals. Or a witch would use something like deadly nightshade to poison someone. See http://www.dogma.org/femmegothique/intro.htm and look for the words "Deadly Nightshade" on this neo-witch site. Unfortunately the site has been taken down but there still is a link on the host site that still has the words "deadly nightshade" but the link will be dead. I don’t know how much longer it will remain. See Richard Restak MD’s book called "Receptors" for a detailed discussion of how witches used to use anticholinergic drugs and how the myth that a witch could fly on a broomstick came about.
Also these neuroleptics drugs can be very sedating making one sleep a lot. Witches used such drugs as a means of control over people in the past. This fact is revealed in the Disney fairy tell "Snow White and the Seven Dwarfs". The evil queen who was also a witch soaked an apple in a cauldron of mind altering chemicals and tricked Snow White into eating it and she fell asleep. Also in the Disney fairy tell "Sleeping Beauty" the witch poisoned the prick of a spindle and used hypnosis to get the princes to prick her finger on it and she fell asleep. In the movie "The Wizard of Oz", the "wicked witch of the west" caused Dorothy and company to fall into a deep sleep by means of spreading a poison dust over a field of flowers which Dorothy and the Lion breathed in because the scent of the flowers inspired deep inhalation. There is symbolism here as well because the flowers are the opium poppy the source of codeine, morphine and heroin. These drugs except the last one have been a favorite of doctors for years. Granted these are just "stories" but stories have basis in fact. See sub-footnote A for a tangential discussion of the wizard in the movie "The Wonderful Wizard of Oz" and Freemasonry.
The psychiatrist witches want to turn you into Sleeping Beauty with a figurative poison apple, a neuroleptic drug. Psychiatrist have been known to put the neuroleptics into the juice of "patients" who were refusing to take the drugs "voluntarily" and the nurses would offer it to the "patient" who unknowingly would consume the poison. Believe me, I speak from experience. The hospital this happened to me at was Grand View Hospital in Dayton Ohio. I also read in a medical book under one neuroleptic how the author described how easily Depakene could be added into the food of a "noncompliant patient".
The Bible book of Revelation states at chapter 21 verse 8 this: "But the fearful, and unbelieving, and the abominable, and the murderers, and whoremongers, and sorcerers, and idolaters, and all the liars, shall have their part in the lake which burneth with fire and brimstone: which is the second death." Revelation 22:15 says: "For without are dogs, and sorcerers, and whoremongers, and murders, and idolaters, and whosoever loveth and maketh a lie." These two scriptures are quoted out of the King James Version of the Holy Bible. The New World Translation of the Holy Scriptures reads as follows: Revelation 21:8 "But as for the cowards and those without faith and those who are disgusting in their filth and murderers and fornicators and those practicing spiritism and idolaters and all the liars, their portion will be in the lake of fire that burns with fire and sulphur. This means the second death." Revelation 22:15 "Outside are the dogs and those who practice spiritism and the fornicators and the murderers and the idolaters and everyone liking and carrying on a lie."
Notice that the King James Version uses the word sorcerers and the New World Translation uses the phrase "those practicing spiritism". To understand the root meaning of this word it will be necessary to look up the word sorcerers in The New Strong's Exhaustive Concordance Of The Bible (King James Version) by James Strong, LL.D., S.T.D. Copyright 1890. After finding the word sorcerers in the index you will see these two scriptures of Revelation listed. There will be two numbers which are 5332 and 5333 on the far right where sorcerers is indexed. You will need these numbers to locate the original Greek words in the Greek Dictionary in the back of this book. You will notice in this dictionary will be listed different grammatical forms of this Greek word from number 5331 to 5333. They are pharmakeia, pharmaeus, pharmakon, and pharmakos. These are the same Greek words that the English words pharmacy, pharmacist, pharmacology, pharmaceutical, pharmacist, phramacopoeia or pharmacopeia, etc. are derived from. In the dictionary at the back of this book it will say the Greek words above mean, druggist or poisoner, magic (magick), sorcerer, magician, witchcaft. If you are not a Christian and you are faced with involuntary drugging now would be a good time to convert. If you are already a Christian and face involuntary drugging but didn't know this Bible teaching from God then don't blame yourself, you know now.
The older version of the MD hypocratic oath was addressed to false pagan gods. Also the symbol that medical doctors (MD not DO) use of two snakes wrapped around a pole is pagan in origin. To see this symbol used by the Medical Society that MDs belong to go to this web-site: http://www.drkoop.com Here is a Satanic Witchcraft illustration taken from the web. Notice that this same medical drug symbol is in the goat of mendes lap. To understand the symbolism of some of this such as the candle on this goats head it will be necessary to go to these web-site resources. http://www.cuttingedge.org/news/n1165.cfm and http://www.cuttingedge.org/n1040.html and http://www.cuttingedge.org/goathead.gif and http://www.cuttingedge.org/n1081.html and http://www.cuttingedge.org/news/n1164.cfm and http://www.cuttingedge.org/news/n1165.cfm .
Tell the judge that as a Christian it violates your religious faith to allow witchdoctors to practice witchcraft on you. Explain what you have learned. According to the Religious Freedom Restoration Act in the USA the judge must follow certain guidelines when you raise this objection, however it has come to my attention that the Supreme Court has ruled this act as "unconstitutional". To find out about this Trojan Horse go to this web-site, http://www.lex-rex.com/newpg.html and http://erlc.com/RLiberty/RFRA/1997/625SupCt.htm. Despite this act being shot down you still have religious liberties granted by the constitution of the USA and can still appeal based on your constitutional rights. Also it is illegal for them to label any religious belief a "delusion" and it is illegal for them to "treat" you based on your religious beliefs labeled as "delusions".
If the judge doesn't allow you to exercise your religious liberties by allowing you to remain drug free then file and appeal. If it is difficult for you to remember this information then just print it out so you can read it to the court and tell them these are your beliefs as a Christian.
Remember the web-sites above and look up Leviticus 17:7 which says "And they shall no more offer their sacrifices unto devils, after whom they have gone a whoring. This shall be a statute for ever unto them throughout their generations." King James Version. This is how this same scripture reads in the New World Translation: "So they should no longer sacrifice their sacrifices to the goat shaped demons with which they are having immoral intercourse. This will serve as a statute to time indefinite for you, throughout your generations." The big difference in these two translations is the use of "devils" verses the phrase "goat shaped demons". To find out why the New World Translation rendered this scripture this way it will be necessary to reference the Strong's Exhaustive Concordance of the King James Bible Again. Look up devils in the index and find this scripture and see the number 8163? Take this number and look in the back of this book in the Hebrew and Chaldee Dictionary and find the number 8163. This will be the original Hebrew word translated into devils in the King James Version of the Holy Bible. Notice that the Hebrew word is saweer' which means shaggy; as noun, a he-goat; by anal. A faun: - devil, goat, hairy, kid, rough, satyr. This is the same satyr in the Disney cartoon Hercules. Isaiah 13:21 speaks of "dancing satyrs" in the King James Version and the New World Translation speaks of "goat shaped demons skipping about". The mythological figure named Pan was a satyr, a half man half goat creature depicted with a musical pipe and dancing about. According to Dr. Anton LaVey author of the Satanic Bible, Freemason and founder of the Church of Satan, Pan and Lucifer are two of the many "infernal" names of Satan the Devil. There are other names listed in the Satanic Bible but these are listed only as support for this footnote. Here is the web-site of the Church of Satan http://www.churchofsatan.com or http://www.churchofsatan.org and the Satanic Network http://www.satannet.com .
For the truth about Jehovah God’s Holy Word the Bible please visit http://www.watchtower.org and fill out the online form to request information. A wonderful paradise on Earth awaits all who put their trust in Jehovah and serve Him. He is going to set up a Kingdom on Earth through His son JESUS Christ as King for a thousand years. Armageddon is close so please look to Jehovah before it is too late. True Christians do not support any political party and do not vote. True Christians do not give their allegiance to any nation on the Earth but to Jehovah’s coming Kingdom on Earth. True Christians do not take up arms and go to war.
Sub-footnote A: It is interesting to note that the wizard (In the movie "The Wonderful Wizard of Oz") who claims to be a good man seems to be a Freemason because he speaks of going back to the land of "E Pluribus Unum" so he can be with his "brother wizards", not fellow but "brother" which is what freemasons call each other and freemasons practice the occult what they call the "craft" (Witchcraft). "E Pluribus Unum" means one out of many which is originally all the states of the USA but around the pyramid on the back of the one dollar bill are the words "Annuit Coeptis Novus Ordo Seclorum" which means Announcing the Creation New Secular (or World) Order. The Freemasons are the ones responsible for everything on the back of the one dollar bill. It is interesting to note that the pyramid has thirteen rows of bricks, the shield on the eagle has thirteen stripes, and the eagle holds thirteen arrows and an olive branch that has thirteen leaves and also thirteen olives. There are thirteen stars above the eagle. There are thirteen letters in "Annuit Coeptis" above the pyramid and thirteen letters in "E Pluribus Unum" above the eagle. In Washington DC the thirty three degree Freemason lodge is thirteen blocks North of the Whitehouse. On the back of the one dollar bill the eagle has thirty two feathers on one side representing the thirty two degrees of Freemasonry Scottish Rite and on the other side thirty three feathers for the honorary degree for which one is initiated into the Illuminati. The tail has nine feathers representing the nine additional honorary degrees of the York Rite of Freemasonry. To understand what the pyramid and the eye represents it will be necessary to visit www.maitreya.org and see the document called "Master Plan for Planet Earth" and also see the gratuitous use of the term "World Order". Freemasons are behind the "Mission of Maitreya" and also the United Nations backed "Share International" run by the British theosophist Benjamin Crème. The Mission of Maitreya is claiming no previous affiliation with the UN backed Share International and Benjamin Crème but is inviting them to join them. Crème had always maintained that he was in direct contact with Maitreya telepathically and that Maitreya would make his presence known at anytime. This is a ruse to make it look like things are happening as Benjamin Crème foretold. For more information see the links below.
Footnote D: This brings
to mind a story that a man at the FDA told me of how a women he knew of that was
institutionalized because her husband who was a doctor pulled some strings with
connections he had, because he was having an affair with another woman. This man
at the FDA told me that when this woman had gotten out of the institution in her
late 30's after years of being forced to take neuroleptics she had already gone
through menopause and her back was humped over with the characteristics of an
old woman. This same man at the FDA told me that the FDA does not conduct animal
studies to determine how these drugs affect the duration of life span nor do
they require the pharmaceutical companies to do so. Does this shock you? After
all the FDA is supposed to be charged with protecting the safety of the American
public. It would be a simple thing to conduct such studies on animals.
Personally I knew of two young women being held in the state hospital in Dayton
Ohio against their will and being forced to take neuroleptics that have already
had to have hysterectomies because of these drugs. One of these women is now out
of this state institution and I do not know the status of the other woman at
For the illustration scans spoken of above get them from the web-sites above.
The following is an
article by Anton Chaitkin that I took from the Internet. The article contains
informative information that helps to understand the impetuous behind the
conspiracy involving these neuroleptic drugs.
Nazis, and the U.N!
by Anton Chaitkin
ROCKEFELLER AND MASS MURDER
The Rockefeller Foundation is the prime sponsor of public relations for the United Nations' drastic depopulation program, which the world is invited to accept at the UN's scheduled September conference in Cairo, Egypt.
Evidence in the possession of a growing number of researchers in America, England, and Germany demonstrates that the Foundation and its corporate, medical, and political associates organized the racial mass murder program of Nazi Germany.
These globalists, who function as a conduit for British Empire geopolitics, were not stopped after World War II. The United Nations alliance of the old Nazi rightwing with the New Age leftwing poses an even graver danger to the world today than the same grouping did in 1941.
Oil monopolist John D. Rockefeller created the family-run Rockefeller Foundation in 1909. By 1929 he had placed $300 million worth of the family's controlling interest in the Standard Oil Company of New Jersey (later called "Exxon") to the account of the Foundation.
The Foundation's money created the medical specialty known as Psychiatric Genetics. For the new experimental field, the Foundation reorganized medical teaching in Germany, creating and thenceforth continuously directing the "Kaiser Wilhelm Institute for Psychiatry" and the "Kaiser Wilhelm Institute for Anthropology, Eugenics and Human Heredity." The Rockefellers' chief executive of these institutions was the fascist Swiss psychiatrist Ernst Rudin, assisted by his proteges Otmar Verschuer and Franz J. Kallmann.
In 1932, the British-led
"Eugenics" movement designated the Rockefellers' Dr. Rudin as the
president of the worldwide Eugenics Federation. The movement called for the
killing or sterilization of people whose heredity made them a public burden.
The Racial Laws
A few months later, Hitler took over Germany and the Rockefeller-Rudin apparatus became a section of the Nazi state. The regime appointed Rudin head of the Racial Hygiene Society. Rudin and his staff, as part of the Task Force of Heredity Experts chaired by SS chief Heinrich Himmler, drew up the sterilization law. Described as an American Model law, it was adopted in July 1933 and proudly printed in the September 1933 Eugenical News (USA) with Hitler's signature. The Rockefeller group drew up other race laws, also based on existing Virginia statutes. Otmar Verschuer and his assistant Josef Mengele together wrote reports for special courts which enforced Rudin's racial purity law against cohabitation of Aryans and non-Aryans.
The "T4" unit
of the Hitler Chancery, based on psychiatrists led by Rudin and his staff,
cooperated in creating propaganda films to sell mercy killing (euthanasia) to
German citizens. The public reacted antagonistically: Hitler had to withdraw a
tear-jerker right-to-die film from the movie theaters. The proper groundwork had
not yet been laid.
Under the Nazis, the German chemical company I.G. Farben and Rockefeller's Standard Oil of New Jersey were effectively a single firm, merged in hundreds of cartel arrangements. I.G. Farben was led up until 1937 by the Warburg family, Rockefeller's partner in banking and in the design of Nazi German eugenics.
Following the German invasion of Poland in 1939, Standard Oil pledged to keep the merger with I.G. Farben going even if the U.S. entered the war. This was exposed in 1942 by Sen. Harry Truman's investigating committee, and President Roosevelt took hundreds of legal measures during the war to stop the Standard-I.G. Farben cartel from supplying the enemy war machine.
In 1940-41, I.G. Farben built a gigantic factory at Auschwitz in Poland, to utilize the Standard Oil/I.G. Farben patents with concentration camp slave labor to make gasoline from coal. The SS was assigned to guard the Jewish and other inmates and select for killing those who were unfit for I.G. Farben slave labor. Standard-Germany president Emil Helfferich testified after the war that Standard Oil funds helped pay for SS guards at Auschwitz.
In 1940, six months after the notorious Standard-I.G. meeting, European Rockefeller Foundation official Daniel O'Brian wrote to the Foundation's chief medical officer Alan Gregg that "it would be unfortunate if it was chosen to stop research which has no relation to war issues" so the Foundation continued financing Nazi "psychiatric research" during the war.
In 1936, Rockefeller's Dr. Franz Kallmann interrupted his study of hereditary degeneracy and emigrated to America because he was half-Jewish. Kallmann went to New York and established the Medical Genetics Department of the New York State Psychiatric Institute. The Scottish Rite of Freemasonry published Kallman's study of over 1,000 cases of schizophrenia, which tried to prove its hereditary basis. In the book, Kallmann thanked his long-time boss and mentor Rudin.
published in 1938 in the USA and Nazi Germany, was used by the T4 unit as a
rationalization to begin in 1939 the murder of mental patients and various
"defective" people, perhaps most of them children. Gas and lethal
injections were used to kill 250,000 under this program, in which the staffs for
a broader murder program were desensitized and trained.
In 1943, Otmar Verschuer's assistant Josef Mengele was made medical commandant of Auschwitz. As wartime director of Rockefeller's Kaiser Wilhelm Institute for Anthropology, Eugenics and Human Heredity in Berlin, Verschuer secured funds for Mengele's experiments at Auschwitz from the German Research Council. Verschuer wrote a progress report to the Council: "My co-researcher in this research is my assistant the anthropologist and physician Mengele. He is serving as Hauptstuermfuehrer and camp doctor in the concentration camp Auschwitz.... With the permission of the Reichsfuehrer SS Himmler, anthropological research is being undertaken on the various racial groups in the concentration camps and blood samples will be sent to my laboratory for investigation."
Mengele prowled the railroad lines leading into Auschwitz, looking for twins -- a favorite subject of psychiatric geneticists. On arrival at Mengele's experimental station, twins filled out "a detailed questionnaire from the Kaiser Wilhelm Institute." There were daily drawings of blood for Verschuer's "specific protein" research. Needles were injected into eyes for work on eye color. There were experimental blood transfusions and infections. Organs and limbs were removed, sometimes without anesthetics. Sex changes were attempted. Females were sterilized, males were castrated. Thousands were murdered and their organs, eyeballs, heads, and limbs were sent to Verschuer and the Rockefeller group at the Kaiser Wilhelm Institute.
In 1946, Verschuer wrote
to the Bureau of Human Heredity in London, asking for help in continuing his
In 1947, the Bureau of Human Heredity moved from London to Copenhagen. The new Danish building for this was built with Rockefeller money. The first International Congress in Human Genetics following World War II was held at this Danish institute in 1956. By that time, Verschuer was a member of the American Eugenics Society, then indistingishable from Rockefeller's Population Council.
Dr. Kallmann helped save
Verschuer by testifying in his denazification proceedings. Dr. Kallmann created
the American Society of Human Genetics, which organized the "Human Genome
Project" -- a current $3 billion physical multiculturalism effort. Kallmann
was a director of the American Eugenics Society in 1952 and from 1954 to 1965.
In the 1950s, the Rockefellers reorganized the U.S. eugenics movement in their own family offices, with spinoff population-control and abortion groups. The Eugenics Society changed its name to the Society for the Study of Social Biology, its current name.
The Rockefeller Foundation had long financed the eugenics movement in England, apparently repaying Britain for the fact that British capital and an Englishman-partner had started old John D. Rockefeller out in his Oil Trust. In the 1960s, the Eugenics Society of England adopted what they called Crypto-eugenics, stating in their official reports that they would do eugenics through means and instruments not labeled as eugenics.
With support from the Rockefellers, the Eugenics Society (England) set up a sub-committee called the International Planned Parenthood Federation, which for 12 years had no other address than the Eugenics Society.
This, then, is the
private, international apparatus which has set the world up for a global
holocaust, under the UN flag. [For more information about the Planned Parenthood
and Rockefeller connection to AIDS and disinformation campaigns, read the book
"Emerging Viruses: AIDS & Ebola--Nature, Accident or Intentional?"
by Dr. Leonard Horowitz (Tetrahedron Press, 1996).]
End of article.
Here is another article for further insight into the eugenics conspiracy by Matt Burg. Also taken from the internet.
Bayer, Hoechst AG, IG Farben and Nazi Germany
By Matt Burg
In 1945 the German army surrendered to the allied powers ending World War 2 in Europe. WWII left Germany humiliated and economically devastated.
The Nuremberg trials were conducted to punish those who had committed acts against humanity. I.G. Farben, the corporation that provided the German army with the gas Zyklon B used to exterminate over 6,000,000 Jews was found guilty of war crimes. The International Military Tribunal ordered the corporation to disband. The result of the disbanding of I.G. Farben was the creation of several smaller corporations. One of these corporations called Hoechst AG grew to become a prosperous company with many subsidiaries. Hoechst AG did not die like the court had intended.
In 1980 a group of French scientists accidentally synthesized a molecule that chemically resembles the hormone progesterone. This molecule has a unique ability to bond the progesterone receptor cells and block their normal activity. The result of the molecule's activity is to block the hormone progesterone, vital to maintaining a pregnancy. The Drug was not invented with the goal of terminating pregnancy, however by the time it was synthesized there was the demand for a new and simplified abortion technique.
The drug first entered the spotlight in 1982 and the controversy erupted shortly after. In 1988 the after extensive testing the French government accepted Mifepristone for public use. The drug is now commonly known as RU 486, the name assigned by the inventor Rousell-Uclaf, a division of the chemical company Hoechst AG. The drug was removed from circulation in France only a month after it was released for public use. The drug was removed by Rousell's CEO Wolfgang Hilger; a devout Catholic after Rousell Uclaf was flooded with letters from outraged Roman Catholic doctors, and after Church-sponsored protests marched through the streets of Paris. The drug was returned to circulation after a group of Pro-Choice Doctors met in Rio de Janeiro and petitioned the French Government. Less than 48 hours later the French Government forced Roussel Uclaf to return the drug to circulation.
RU 486 will allow Rousell Uclaff, a division of Hoechst AG to increase the corporation's production in America. The company has deeper intentions than what is obvious. Hoechst AG a company with deep roots in the Nazi party intends to control the population of the world and eliminate the lesser races as Hitler intended through the use of RU 486 and the World Health Organization.
Rousell Uclaff is a division of Hoechst AG, a large worldwide chemical corporation that was founded in 1863 in Germany. This small company with, only 5 employees, manufactured chemical dyes. In 1925, several German chemical companies merged into a single corporation with the name IG Farbenindustrie, Inc. (IG Farben) World War I created a demand for chemical products. After WWI, the devastated German government gave IG full government support by eliminating taxes and loaning the company funds. In 1925, the company changed it's to IG Farbenindustrie A. G. IG became one of the military industrial powers of the Ruhr, owning its own coalmines.
In 1932 IG gave Adolf Hitler its full support during the election and so Hitler was presented with the Chancellorship of Germany. Without the support of the IG and the rest of the German monopolies and cartels, Hitler could not have won his political fight. And the German industrialists could see that without Hitler their empires would crumble. During WWII IG produced all of Germany's synthetic rubber, lubricating oil, synthetic gasoline, the greatest bulk of German explosives, 90% of plastics, and light metals. More than any other corporation IG sat at the center of a web of international cartel agreements. IG participated in the plunder of conquered countries including Austria, Czechoslovakia, Poland, Norway, Holland, Belgium, France and the rest of Central Europe. IG took over control of every chemical plant of importance in countries conquered by the Nazi Empire. IG played an important role in adapting the industries of those countries to the purposes of the Nazi war machine.
IG Farben ran the Buna Rubber Works at Auschwitz by opening a corporate concentration camp known as Monowitz on May 21, 1945. I.G Farben used slave labor extensively in many of their factories throughout the Nazi Empire.
IG was a big part in developing chemical/gas warfare. Toxic gases were produced at Hoechst, Afga and Leverkusen plants.
IG produced fully 95% of
the poison gases for Germany. It was called Zyklon B, a commercial form of
hydrocyanic acid, which became active on contact with air. It was manufactured
by a firm called Degesch which was largely owned by IG Farben, and it had been
brought to Auschwitz in the summer of 1941 as a vermin-killer and disinfectant.
In 1945, when the International Military Tribunal was announced and began trying Nazi officials for crimes committed during WWII, the list of crimes which one could be indicted were as follows:
(1) Conspiracy to commit
charges 2, 3, and 4, which are listed here;
(2)crimes against peace-defined as participation in the planning and waging of a war of aggression in violation of numerous international treaties;
(3) war crimes-defined as violations of the internationally agreed upon rules for waging war; and
(4) crimes against humanity-"namely, murder, extermination, enslavement, deportation, and other inhumane acts committed against any civilian population, before or during the war; or persecution on political, racial, or religious grounds in execution of or in connection with any crime within the jurisdiction of the Tribunal, whether or not in violation of domestic law of the country where perpetrated."
On July 29, 1948, sentences for mass murder and slavery were handed down at the Nuremberg trials to twelve Farben executives. The longest sentence dealt out was to Dr. Fritz ter Meer, a top executive and scientist on the Farben managing board was seven years. After WWII, IG Farben was liquidated and the companies like Bayer, Hoechst, BASF, and AFGA took its place.
In 1949, less than a year after the Nuremberg Trials had ended; Hoechst AG opened a branch in Brazil. The company offered the whole representation of products in Brazil by establishing Pontosan Productos Quimicos, Farmcuticose e Aniilianas and appointed Wilhelm Kurtz as President. The company rapidly expanded and manufactures products ranging from pharmaceuticals to welding and cutting equipment. In 1995 Pontosan Productos Quimicos, Farmcuticose e Aniilianas acquired the company Anilsud, formerly owned by Hoechst Argentina forming an Argentine branch. Today, Pontosan Productos Quimicos, Farmcuticose e Aniilianas renamed Hoechst Commercial is one of the leading companies for the distribution of chemicals in Brazil.
Hoechst International headquartered in Frankfurt, Germany with branches in Asia, Oceania and America. Hoechst employs more than 145 thousand people. Hoechst is one of the largest groups in the chemical industry, with sales of approximately US$ 13158 in DM billions for the first quarter of 1997.
Methods of Action Mifepristone resembles the hormone progesterone yet it has a far different effect on the progesterone receptor cells. Progesterone is a hormone secreted by the uterus when a female gets pregnant. The hormone is vital to maintaining the pregnancy because it stimulates the endometrial lining to supply the embryo with nutrients. Mifepristone is given in 600mg doses When mifepristone enters a progesterone receptor cell, the molecule blocks any further action of the hormone progesterone making the body act as if it were not even pregnant. The lack of progesterone causes erosion of the endometrial lining and so the embryo dies. Two days later Prostaglandin is taken which causes the uterus to contract and will expel the embryo in 97% of the cases. Mifepristone is effective for up to seven weeks after coitus.
Mifepristone has several side effects of varying degrees. Use of Mifepristone can cause heavy bleeding, nausea, vomiting, fatigue, and painful uterine contractions. About 2% hemorrhage and more than one in one hundred require hospitalization. Mifepristone effectively terminates pregnancy about 95% of the time. Researchers have found that mifepristone is 99% effective in preventing pregnancy when used as a method of postcoital contraception if used within 72 hours after unprotected intercourse.
In 1983, clinical trials on the use of RU 486 as a method of early abortion began in the U.S. at the University of Southern California, Five years later, Mifepristone was "approved" by the French government forcing the entire country to choose a side on the moral debate. The outrage from members of the Roman Catholic Church brought Roussel Uclaf to their knees and prevented the drug from further circulation. Three days later, the combined efforts of various physicians convinced the French government to force Rousell Uclaf to return the drug to circulation. Anti-abortion forces threatened Roussel Uclaf's parent company, Hoechst AG, with economic reprisal if RU 486 was ever marketed in the United States. In March of 1989, Hoechst informed the anti-abortion forces that the company had no intention of marketing or distributing RU 486 outside of France. President Bush responding to his pro-life platform along with fellow anti-abortion congressional representatives enacted a ban on the importation of RU 486 for personal use.
In July of 1990 the Feminist Majority Foundation delegation met with Rousell Uclaff CEO Edouard Sakiz. Eleanor Smeal, acknowledged as one of America's rights advocates, and Peg Yorkin, a prominent feminist producer and philanthropist founded the FMF in 1987. The organizations with 150,000 male and female members stand up for women's rights (including reproductive rights), equality, and empowerment. Hoechst AG Officials argued that the U.S. political climate is not conductive to U.S. distribution because the current administration had banned the importation of the drug and as the current views of the administration on abortion, distribution was not possible.
In February of 1991, the American Association for the Advancement of Science (AAAS) endorsed the testing and use of RU 486. With the support of the AAAS, the FMF aggressively and successfully pursued endorsements of RU 486 from almost every scientific and medical organization in the country.
In July of 1992, the first direct challenge of the FDA import alert on RU 486. Last year a pro-choice group called Abortion Rights Mobilization decided to force a court challenge of the import ban imposed on RU 486 (Mifepristone) by the Bush Administration in 1989. The organization helped Leona Benton, a pregnant 29-year-old California social worker, fly to England, obtain a dose of RU 486, then try to bring it back into the U.S. through New York City's Kennedy Airport. Customs officials seized the pills. The ensuing legal battle went up to the Supreme Court, which refused to order the government to return the pills. (The Pill that changes Everything, Pg. 52)
On November 4, 1992, Bill Clinton was elected President of the United States. The FMF immediately sent a letter to a Rousell Uclaf CEO Edouard Sakiz and Hoechst AG CEO Wolfgang Hilger informing them that with Clinton's election and the election of more women and pro-choice members of Congress the political obstacles to RU 486 in this country had "effectively been removed."
FMF is not alone in the legalization debate, other organization who support mifepristone in America are Planned Parenthood Federation of America, a government funded organization specializing in sex and reproductive education. Planned Parenthood Clinics provide pregnancy tests, birth control and abortion services. The organization is also an avid supporter of reproductive rights.
The National Organization for Women is another supporter of mifepristone in America. NOW is a strong supporter of Abortion and Reproductive rights. Now has strongly urged the United States Government to approve mifepristone in America.
There are many organizations that strongly oppose mifepristone in America. The National Right to Life Committee is a strong force in the Abortion debate. The NRLC supports the right to life in all cases including Euthanasia and Abortion.
The National Conference of Catholic Bishops' Committee for Pro-Life Activities is a group of eight active U.S. Cardinals who influence the government according to the doctrine of the Roman Catholic Church. They oppose abortion in all forms stating that life is sacred from conception to birth.
Hoechst and the United Nations
In October of 1996, the United Nations/World Health Organization Codex Alimentarius Commission met in Bonn, Germany to make changes in the rules governing dietary supplements for member nations. Codex is empowered by governments to set standards of operation for the health industry. Over 90% of the international organization are allowed to send delegates to the meetings to represent large multinational pharmaceutical corporations. A proposal made by the German delegation and sponsored by Hoechst, Bayer and BASF the three corporations that were formerly IG Farben before they were ordered to disband after the Nuremberg Trials. The drug company backed proposals call for the following:
1) No vitamin, mineral,
herb, etc., can be sold for prophylactic (preventive) or therapeutic reasons.
2) Natural remedies can be sold as food but they must not exceed the potency levels set by the commission. This means that consumer access to dietary supplements will be limited to the RDA dosage as a maximum limit for vitamins. Supplements without a RDA would be illegal to sell because they would become drugs.
3) Codex regulations for dietary supplements would become binding, eliminating the escape clause within the General Agreement of Tariff and Trade (GATT) that allows a nation to set its own standards will be heavily fined by the World Trade Organization (WTO) creating the potential of crippling the entire sectors of that nation's economy.
4) All new supplements would be banned unless they go through the Codex approval process.
This policy is has been enacted in Norway and Germany. This policy if approved would cause pharmacy regulation of many supplements and vitamins causing a signifigant price increase. Any country not following the policy would be subject to fines from the World Trade Organization.
The Codex process is now
at "Step Five"- formalization and debate concerning the specific
features of the policy. In two years, Codex could jump from step 5 to step8 to
finalize the restrictions.
Hoechst AG a company with deep roots in the Nazi party intends to control the population of the world and eliminate the lesser races as Hitler intended through the use of RU 486 and the World Health Organization. Hoechst AG intends to get RU 486 approved for manufacturing and distribution in America and other countries worldwide so that they can use it to achieve goals further down the road. In 1949 with the disbanding of the formerly IG Farben Corporation into smaller corporations was not set back to Hoechst or any of the other corporations. The corporations could continue to business and the International Military Tribunal had almost helped the corporations out by making them split up.
This helped them in several ways, first the corporations were no longer known by the less than desirable name of IG Farben Corporation the former supporter of Hitler and the German army. Second of all, using the "divide and conquer " tactic, the smaller corporations quickly spread to other countries where they purchased small corporations and used the identity of the smaller corporations to increase sales and profits. The main example of this was the spread of Hoechst AG to Brazil. Less than a year after the Nuremberg Decision had been reached; Hoechst AG had already begun to rebuild in Brazil. This was the first evidence that the liquidation of IG Farben had not worked. The new corporation quickly began to purchase smaller corporations and added them to the increasing list of corporations owned by Hoechst AG International.
Hoechst is an extremely rich and powerful International corporation. The reason why they are building and expanding their branches in new countries is so they can market mifepristone in many countries worldwide. Hoechst will not only achieve financial gain through their expansion but they will also have more control over the countries that they supply with mifepristone.
Hoechst's real motive eludes the groups supporting RU 486 in America. Hoechst's attempts to market mifepristone in America through it's subsidiary Rousell Uclaff could not have come at a better time. The company knew that the Clinton administration supported abortion and reproductive rights so they simply waited until the atmosphere in the country was a bit more to their liking. Using the support from groups like the Feminist Majority Foundation and the National Organization for Women Hoechst would not need Hoechst's ultimate goal is to increase production worldwide of RU 486 to gain representation in the Codex. Because Codex representation is based on nationality, the more countries that Hoechst manufactures in, the more representation in Codex they get. Hoechst can gain representation in the Codex and essentially can control the Global Health Market. Control over the global health market would allow Hoechst to gain control of Global Health Care.
The approval mifepristone in several UN countries would make it much easier for Hoechst to distribute the drug worldwide. If the drug is already legal in the majority of the UN countries then Hoechst will have to do little convincing to get the drug approved in the other countries. This is why Hoechst is attempting to market mifepristone in America and is already manufacturing and distributing the drug in the United Kingdom and in China.
The money and power held by Hoechst could easily influence the World Health Organization which would allow Hoechst to dictate World Health Policy. The backup support of the World Trade Organization would make it almost impossible for any country to oppose the policies influenced mainly by Hoechst.
The corporation would become so powerful that they could regulate the use of mifepristone. They would be able to control who was allowed to use mifepristone and who was not allowed to use mifepristone. Hoechst, with their power and influence could bring the Nazi party back into power in order to continue Hitler's goal of establishing the "perfect race". No longer would they need to use Zyklon B to exterminate the "undesirables."
When a female got pregnant they could simply have her take a dose of Mifepristone and they would not have to waste the time or money to eliminate the "undesirables" by means of lethal force. Hoechst could simply make all of the races other than the Aryan race slowly deplete in number and then simply go extinct. The unfinished goals of World War 2 would be taken care of. There would finally be an end to the Jewish problem. The "perfect race" would rule the World for the rest of Mankind's existence.
Mifepristone could become
a problem very quickly. Population control is the final explanation for
mifepristone. Humans need to learn to be responsible for their own actions. In
order to prevent history from repeating itself, we need to make sure that humans
never become so irresponsible that an outside force such as Hoechst can come in
and take control. Hitler did it once, let's not let it happen again.
Here is an article taken from the web dealing with eugenics. Author is unknown.
Eugenics is false science. It is about the selective prevention or encouragement of births for social, racial, or political ends. When promoting anti-natalist measures, such measures are often hidden beneath rhetoric about freedom of choice or reproductive health. When eugenic goals demand increased fertility, those goals may be advanced in the name of national power, race survival, or even family support programs (including maternity leave, day care, child care allowances, etc. as in much of Europe today) which would be considered progressive if not for the intent behind them.
Eugenics is not about reproductive freedom. It is, in fact, the antithesis of reproductive freedom because it is essentially concerned with competitive fertility. As such, it is similar to -- but not identical to -- population control. The distinction here is that eugenics supplies a biological or genetic interpretation to its means and aims. If it is a particular race that is to targeted, for instance, the eugenicist will first offer a "scientific" basis for such a plan -- usually consisting of statistical "evidence" that the disfavored group is less capable of achievement, more prone to anti-social behavior, or otherwise disproportionately responsible for a prevalent social problem. Most importantly, the eugenicist will insist that this "inferiority" is hereditary -- that "excessively" high birthrates among these people will lead to a general decline in the quality of the society as a whole.
Thus the eugenicist will believe it a legitimate and necessary public policy that minimizes procreation among certain groups (sometimes coinciding with the promotion of greater fertility among other segments of the population).
It should be added that an activity designed to influence levels of fertility is not the only tactic available for use under a eugenic program. High rates of incarceration (especially where a large number of young adults are concerned) may be tolerated precisely because imprisonment results in a loss of reproductive opportunity. Eugenic goals also extend to immigration when an incoming population is defined in some "scientific" way as socially inferior or if an exclusion policy selects by ethnicity or class. As was made abundantly clear under the Nazi program of mass genocide, a well-functioning eugenics operation is never satisfied for long with modest results. It is almost inevitable that the escalation of what is deemed a "useful" activity will be seen advocates as "more useful."
The word eugenics comes from the Greek for "good genes." Therefore, any policy that is thought by advocates to stimulate the prevalence of "good genes" is considered eugenic in its effect. Another term -- dysgenic is applied to a situation in which the undesirable elements grow at a greater rate than the rest.
Finally, it should be pointed out that eugenics can be broken down into several distinct philosophies. Social Darwinism is a term commonly applied to class-based eugenics. The operative theory here is that wealth is spontaneously distributed throughout the society according to the merits of the individuals within the society. In other words, adherents believe the wealthy are rich because of inherent traits that make them productive members of the community. The poor, on the other hand, are said to be destined to want precisely because they are of "inferior stock." Thus, in the mind of the eugenicist, any effort to promote economic justice will have a dysgenic effect because it only encourages breeding among these "lesser" types.
This kind of thinking can be found not far beneath the surface of contemporary proposals like the "family cap" for welfare parents, certain campaigns to halt teen pregnancy and the flap about an "illegitimacy." Racial eugenics defines people from different regions of the world as having unique evolutionary characteristics which make one group more suited to certain pursuits than another. This is the ideology behind The Bell Curve and similar publications that have aroused controversy in the past few years.
Some proponents of eugenics cite physical or mental disabilities as cause for limits to reproduction. In terms of policy, they are more interested in stigmatizing the alcoholic, the drug abuser, or the mental patient than in seeking authentic forms of treatment and measures that would influence the economic or social environment in which such problems flourish. This form of eugenics has made inroads into many of the more legitimate sciences such as human genetics and bio-ethics. Indeed, eugenics is especially dangerous in this area because of the opportunity to apply obvious truths -- the fact that children inherit physical features from their parents, to name one -- to political issues, such as "criminal tendencies" or an "underclass" culture, in a way that results in discriminatory policies.