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:
mo...@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. 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.