Psychiatry Kills
Documented Proof Psychiatric Drugs Shorten Life Span
Version 2.012

 By Shemuwel Antoine 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." 

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 eugenics 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: moser@donet.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 founder or "father" of psychiatry in the United States was a Freemason named Benjamin Rush. He was one of the signers of the United States constitution. Psychiatry was founded as a means to take care of critics of Freemasonry or the Masonic Lodge. Also to take care of people who are revealing  "National Security Secrets" and also to take care of people who "step on the big guys toes" by challenging their interests or causing them to loose money. Also to take care of "whistle blowers" and to take care of people who are attempting to change Satan's demon inspired "status quo". "Status Quo" means the generally accepted viewpoint which is often wrong. To take care of true Christians who are discovering truths from the Holy Scriptures and revealing them to the people. The Mason or Freemason named Benjamin Rush invented a restraint chair with straps on it that he named "the tranquilizer" which is where this word originated. He also invented the straight jacket. The electric chair today is a modification of Benjamin Rushes invention. The Masonic Lodge is evil to the core. The Catholic Church is no better because they also run psychiatric wards and coperate with the government to silence people by "taking care of them". The Catholic Church has a lot of stock in the pharmacutical industry which includes psychiatric drugs. Psychiatry has become for the Catholic Church their new means of inquisition and their psychiatric wards in their hospitals are their inquisition halls were people are tortured chemically. I was personally drugged with a double dose of Haldol in the hospital named "Mercy Medical Center" in their emergency room in Springfield Ohio and when I cried out that I was a Jehovah's Witness being drugged by a Catholic hospital they shipped me to the State Mental Health facilities at Twin Valley Behavorial Modification in Dayton Ohio instead of putting me in their own facilities there.

 

A Freemason probate judge by the name of Richard P. Carey sent me by his order to a state mental health facility where I was repeatedly drugged by court order. I told him in court that he was a Freemason and he read a internet site I once had online exposing Freemasonry. It is clear his motives were to attempt to silence me for exposing Freemasonry or the Masonic Lodge. The Masons are very strong in Clark County. For instance Sheriff Gene A. Kelly of Clark County Ohio is a 32 degree Freemason. I know because he admitted it once to me on the telephone. Judge Richard P. Carey is a Freemason Nazi. He attempted to silence me but the Almighty Father Yehovah protected me. USA courts have forced drugs on me many times in the past by court order. But the Almighty Father has protected me and I still have my mind intact and have two new sons by his blessings. Willfull unrepentent poisoners can not enter into the Kingdom of Yehovah Elohim (Jehovah God). See www.watchtower.org for people who can help you rely on the Almighty Father in spirit and truth so you to can recieve the protections of the Almighty Father from wolves like Richard P. Carey Freemason. Once congressman Hobson tried to get me institutionalised because I gave him a copy of this report. That did not work so Sheriff Gene A. Kelly attempted to get my father to institutionalize me. I even got multiple death threats in my E-mail for writing this report and speaking out against Freemasonry on the internet. I want these people to know that I forgive them and pray for them and that they can be forgiven of anything as long as they turn to Yehovah genuine repentance. See www.watchtower.org

 

Judge Richard P. Carey, Clark County Probate Court 50 East Columbia St., 5th Floor, Springfield, Ohio 45502-1194 Phone (937) 328-2437 Fax (937) 328-2589 - Call, Visit, Write or Fax him and let him know your outrage and how you know he acted with injustice.

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 misconstrued 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  Also see http://home.earthlink.net/~bazillion/psych_news.html . 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 Shemuwel Antoine 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.