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Greetings to All,

 

I have erie questions: Years ago, my brother took his life. Since

then, I have been trying to understand something but I'm not certain

what?! I was wondering this morning... does TCM have any treatments

and/or explanations for people that have thoughts of suicide? How do

the Buddhist feel about it? Is it taboo? As you can see, I'm still

seeking for answers...

 

Have a good day, Danamarie

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Danamarie:

 

My brother took his life in 1977, and I was the one to

find his body. The " Sha Qi " that surrounded his

violent death scene immediately clung to me and harmed

my life for the 28 years after that.

 

TCM does have a method to revive those who die by

hanging.

 

I can't speak to Buddhist proscriptions about suicide.

However, I do know about Chinese traditional beliefs

about such matters.

 

Any violent death creates extremely negative energies.

I have heard a contemporary story of a haunted house

in Guangzhou where an entire family was brutally

murdered--leaving behind some extremely negative

energy that sought retribution from the killers.

 

In my brother's case, his soul wandered for 28 years

because no one in my family knew enough to burn spirit

money or perform other necessary ceremonies.

 

This gets into the area of metaphysics and leaves TCM

far behind--no one in TCM today wants to go into this

area. Chinese authorities have been trying for 2000

years to cleave away the shamanic aspects of medicine

and healing, and TCM reflects the same old official

campaign against shamans.

 

I believe the psychological aspects of TCM are quite

useful, even more so than western psychiatry and TCM

could help prevent suicides. My brother suffered

through a decade of mental institutions and horrible

medications that did little to relieve his

schizophrenia.

 

A more gentle and effective TCM approach with

acupuncture and herbs might have made a difference for

him.

 

Regards, Jack

 

--- das4145 <asenat45 wrote:

 

> Greetings to All,

>

> I have erie questions: Years ago, my brother took

> his life. Since

> then, I have been trying to understand something but

> I'm not certain

> what?! I was wondering this morning... does TCM

> have any treatments

> and/or explanations for people that have thoughts of

> suicide? How do

> the Buddhist feel about it? Is it taboo? As you

> can see, I'm still

> seeking for answers...

>

> Have a good day, Danamarie

>

>

>

>

>

>

>

>

 

 

 

 

________

DSL – Something to write home about.

Just $16.99/mo. or less.

dsl.

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This is not TCM, but several years ago there was some promising

research into the use of dialysis for treating some (not all) cases of

schizophrenia. The screens had a different size mesh than those used

in kidney dialysis. I forget if they were finer or coarser.

 

Unfortunately, the pharmaceutical industry heavily funds the American

Pyschiatric Association, and research into dialysis, nutrition, and

other treatments for schizophrenia were abandoned or all but abandoned

in favor of drugs.

 

By the way, some cases of schizophrenia have a factor of an error in

copper metabolism, and these schizophrenics suffer from too much

copper. In many " primitive " societies, the first thing the healers do

when someone starts to display signs of what is called schizophrenia

in the West is to take away all copper jewelry and tools from the

person.

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Chinese Traditional Medicine , Jack Sweeney

<mojavecowboy> wrote:

> In my brother's case, his soul wandered for 28 years

> because no one in my family knew enough to burn spirit

> money or perform other necessary ceremonies.

 

Jack, I hope you will go into this in more detail. Even though it's no

longer a part of officially recognized TCM, I feel like it would be

helpful to some readers on here.

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Victoria:

 

I'd be happy to since you asked.

 

My brother was a devout Catholic and was granted a

Catholic burial, despite his suicide. My family

regarded that as enough.

 

While undergoing acupuncture in China, I told my

doctor about my brother, as well as other phenomena

that I have experience. For example, I now and then

get a tingling sensation down my spine, especially

when I play guitar and sing songs. My doctor's mother

is a practicing shaman, and so my doctor understood

what was happening to me.

 

My brother died a violent death, and so his spirit

wandered in the nether realm for 28 years, without

spirit money, (or spirit clothing or a spirit home).

That really means that his soul was homeless and

bankrupt for that entire period.

 

At the same time, his negative " Sha " Qi was playing a

negative effect on my own life, including personal

health and fortune. Until my brother's situation could

find relief, my own health and fortune were in danger.

 

My doctor arranged for a spiritual ceremony for my

brother, with his mother communicating with the spirit

world, and the doctor performing rites for me in my

home. Basically this involved a rooster, some food,

alcohol and a pile of spirit money.

 

My doctor conducted the ceremony and burned the money

in my apartment. At the time, he said that he could

see my brother, who was very glad to receive the

offerings. His mother reported that things had gone

well on the spirit side.

 

Since that time, my circumstances have improved, and I

learned critical information regarding my own health

condition and how to treat my problems.

 

IMO, there is a spiritual aspect to life that is just

as important as the material, and we need to maintain

a balance, as we would with money in a bank. To become

modern and Western, TCM has severed connections with

the spiritual side of things, to its detriment.

 

In answer to this question of suicide, classical

Chinese medicine's connection with the psychological

aspects, such as the thirteen Ghost Points, as well as

spiritual psychology and Jungian psychology, can have

a profound impact on resolving psychological issues,

before the individual walks the road of despair toward

suicide.

 

Regards, Jack

 

 

 

--- victoria_dragon <victoria_dragon wrote:

 

> Chinese Traditional Medicine , Jack Sweeney

> <mojavecowboy> wrote:

> > In my brother's case, his soul wandered for 28

> years

> > because no one in my family knew enough to burn

> spirit

> > money or perform other necessary ceremonies.

>

> Jack, I hope you will go into this in more detail.

> Even though it's no

> longer a part of officially recognized TCM, I feel

> like it would be

> helpful to some readers on here.

>

>

>

>

>

>

>

>

>

 

 

 

 

________

DSL – Something to write home about.

Just $16.99/mo. or less.

dsl.

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G'day TCMers,

-the following powerful account & links may help many folks

cheers,

dar

 

 

The International Advocates for Health Freedom

is a catalytic entity designed to foster networking between health

freedom activists world wide in order to foster opposition to the

elements of coercion: the UN's International Council of Drug Regulating

Authorities, and all regulating bodies falling under its auspices

including the FDA, TGA, HPB, MCA, MCC etc.

 

The founder of IAHF, John Hammell,

has been fighting professionally for health freedom for 10 years, and

first got involved with alternative medicine after recovering from a

life threatening illness in 1980

via a suppressed alternative treatment mode (orthomolecular medicine)

after mainstream methods almost killed him.

His personal belief is that herbs and other dietary supplements are

gifts to us all from our Creator. As such, he believes it to be highly

immoral for anyone to try to restrict their availability or to do

anything which would hamper consumer access. For more of an insight on

John Hammell read his articles Why I Fight for Health Freedom and Urgent

Appeal From An Orthomolecular Psychiatric Survivor: Vitamin Access

Threatened Globally.....

 

http://www.iahf.com/orthomolecular/orthomolecular.html

 

 

Vital Information Suppressed

Every week I get calls from people interested in learning more about how

I recovered from schizophrenia via orthomolecular medicine. I refer

everyone to Well Mind Assoc of Greater Washington for more info at

301-949-8282. Also check out http://www.orthomed.org/ There are many

good links from that site including one to Dr.Hoffer's homepage at

http://www.islandnet.com/~hoffer/hofferhp.htm

 

It saddens me greatly that this information is being suppressed. Please

forward it widely. Far too much needless suffering is going on. Twenty

years after I recovered people are still being denied access to

orthomolecular treatment, which was first made available way back in 1952.

Due to the suppression of this information, I was forced to spend 4

years in mainstream mental hospitals where they almost killed me with

drugs and really came close a few times. I almost choked to death on my

own saliva once because phenothiazine medication causes you to lose your

gag reflex and choke. I had numerous bloody fights with the goons. The

evil of the pharma cartel is incalculable. The Nazis who are suppressing

this information are the same Nazis who are using Codex to try to

destroy our access to the supplements we need.

 

On the Orthomolecular Environment of the Mind: Orthomolecular Theory

 

" Varying the concentrations of substances normally present in the human

body may control mental disease. " - Linus Pauling

 

" The methods principally used now for treating patients with mental

disease are psychotherapy (psychoanalysis and related efforts to provide

insight and to decrease environmental stress), chemotherapy (mainly with

the use of powerful synthetic drugs, such as chlorpromazine, or powerful

natural products from plants, such as reserpine), and convulsive shock

therapy (electroconvulsive therapy, insulin coma therapy,

pentylenetetrazol shock therapy). I have reached the conclusion that

another general method of treatment, which may be called orthomolecular

therapy, may be found to be of great value, and may turn out to be the

best method of treatment for many patients. " - Linus Pauling, Science,

April 19, 1968, p. 265

 

The author defines orthomolecular psychiatry as the achievement and

preservation of good mental health by the provision of the optimum

molecular environment for the mind, especially the optimum

concentrations of substances normally present in the human body, such as

the vitamins. He states that there is sound evidence for the theory that

increased intake of such vitamins as ascorbic acid, niacin pyridoxine,

and cyanocobalamin is useful in treating schizophrenia. The negative

conclusions of APA Task Force Report 7, Megavitamin and Orthomolecular

Therapy in Psychiatry, he says, result not only from faulty arguments

and from a bias against megavitamin therapy but also from a failure to

deal fully with orthomolecular therapy in psychiatry- Three

psychiatrists comment on Dr. Pauling's presentation.

 

Orthomolecular psychiatry is the achievement and preservation of mental

health by varying the concentrations in the human body of substances

that are normally present, such as the vitamins- It is part of a broader

subject, orthomolecular medicine, an important put because the

functioning of the brain is probably more sensitively dependent on its

molecular composition and structure than is the functioning of other

organs (1) . After having worked for a decade on the hereditary

hemolytic anemias, I decided in 1954 to work on the molecular basis of

mental disease. I read the papers and books dealing with megavitamin

therapy of schizophrenia by Hoffer and Osmond (2,4) as well as the

reports on studies of vitamins in relation to mental disease by Cleckley

and Sydenstricker (5,6) and others. In the course of time I formulated a

general theory of the dependence of function on molecular structure of

the brain and other parts of the body and coined the adjective

" orthomolecular " to describe it (1).

 

There is no doubt that the mind is affected by its molecular

environment. The presence in the brain of molecules of LSD, mescaline,

or some other schizophrenogenic substance is associated with profound

psychic effects. Mental manifestations of avitaminosis have been

reported for several vitamins. A correlation of behavior of school

children with concentration of ascorbic acid in the blood (increase in

" alertness " or " sharpness " with increase in concentration) has been

reported by Kubala and Katz (7).

 

A striking abnormality in the urinary excretion of ascorbic acid after

an oral loading dose was reported for chronic schizophrenics by

VanderKamp (8) and by Herjanic nd Moss-Herjanic (9). My associates and I

(10) carried out loading tests for three vitamins on schizophrenic

patients who had recently been hospitalized and an control subjects. The

percentage of schizophrenic patients who showed low urinary excretion of

each vitamin was about twice as great as that of the controls: for

ascorbic acid, 4 percent of the schizophrenic patients showed low

urinary excretion versus 32 percent of the controls; for niacinamide, 81

percent versus 46 percent; and for yridoxine, 52 percent versus 24

Percent. The possibility that the low values in urinary excretion of the

vitamins for schizophrenic patients resulted from poor nutrition is as

unlikely by the observation that the numbers of subjects low in one,

two, or all three vitamins corresponded well with the numbers calculated

for independent incidence.

 

There are a number of plausible mechanisms by which the concentration of

a vitamin may affect the functioning of the brain. One mechanism,

effective COT vitamins hat serve as coenzymes, is that of shifting the

equilibrium for the reaction of apoenzyme and coenzyme to give the

active enzyme. An example is the effectiveness of yanocobalamin (vitamin

B12) given in amounts 1,000 times greater than normal to control the

disease methylmalonic aciduria (11-14). About half of the patients with

this disease are successfully treated with megadoses of vitamin B12 . In

these patients a genetic mutation has occurred and an altered apoenzyme

that has a greatly reduced affinity for the coenzyme has been produced.

Increase in concentration of the coenzyme can counteract the effect of

the decrease in the value of the combining constant and lead to the

formation of enough of the active enzyme to catalyze effectively the

reaction of conversion of methylmalonic acid to succinic acid.

 

In the human population there may be several alleles of the gene

controlling the manufacture of each apoenzyme; in consequence the

concentration of coenzyme needed o produce the amount of active enzyme

required for optimum health may well be somewhat different for different

individuals- In particular, many individuals may require considerably

higher concentration of one Or more coenzymes than other people do for

optimum health, especially for optimum mental health. It is difficult to

obtain experimental evidence for gene mutations that lead to only small

changes in the properties of enzymes. The fact that genes that lead to

large and more easily detectable hanges in the properties of enzymes

occur, as in individuals with methylmalonic aciduria, for example,

suggests that mutations that lead to small changes also occur.

 

Significant differences in enzyme activity in different individuals have

been reported by many investigators, especially by Williams [15], who

has made many studies of biochemical individuality. It is likely that

thorough studies of enzymes would show them to be similar to the human

hemoglobins. A few of the abnormal human hemoglobins, most of which

involve only the substitution of one amino-acid residue for another in

either the alpha chain or the beta chain of the molecule, differ greatly

in properties from normal adult hemoglobin, leading to serious

manifestations of disease.

 

It was in the course of the study of one of these diseases, sickle cell

anemia, that the first abnormal hemoglobin was discovered (16). Most of

the abnormal human hemoglobins, however. differ from normal hemoglobin

in their properties to only a small extent, so that there is no overt

manifestation of disease. There is, nevertheless, he possibility that

even the small changes in properties of an abnormal hemoglobin

associated with a mild hemoglobinopathy will have deleterious

consequences. An example is the intolerance to sulfa drugs associated

with the substitution of arginine for histidine in the locus 58 in the

alpha chain or 63 in the beta chain. It is likely that individual

differences in enzyme activity will in the course of time be shown to be

the result of differences in the amino-acid sequences of the polypeptide

chains of the poenzymes.

 

More than 100 abnormal human hemoglobins are now known, and the human

population may be expected to be similarly complex with respect to many

enzymes, including those involved in the functioning of the brain. A

tendency to schizophrenia is probably polygenic in origin. I have

suggested (1) that the genes primarily involved n this tendency may well

be those which regulate the metabolism of vital substances such as the

vitamins.

 

Some vitamins are known to serve as coenzymes for several enzyme

systems. We might ask if the high concentration of coenzyme required to

produce the optimum mount of one active enzyme might not lead to the

production of far too great an amount of another active enzyme. The

answer to this question is that the danger is not very great. For most

enzymes the concentration of coenzyme and the value of the combination

constant are such that most (90 percent or more) of the protein is

converted to active enzyme. Accordingly, a great increase in

concentration would increase the amount of most active enzymes by only a

few percentage points, whereas t might cause a great increase for a

mutated enzyme.

 

The Orthomolecular Treatment of Schizophrenia

 

In the book Orthomolecular Psychiatry: Treatment Of Schizophrenia (17)

my colleagues and I pointed out that the orthomolecular treatment of

schizophrenia involves the use of vitamins (megavitamin therapy) and

minerals; the control of diet, especially the intake of sucrose; and,

during the initial acute phase, the use of conventional methods of

controlling the crisis, such as the phenothiazines. The phenothiazines

are not, of course, normally present in the human body and are not

orthomolecular. However, they are so valuable in controlling the crisis

that their use is justified in spite of their undesirable side effects.

 

Hawkins (18) stated that his initial combination of vitamins for the

treatment of schizophrenia was I gin. of ascorbic acid, I gm, of

niacinamide, 50 mg. of pyridoxine, and 400 I.U. of vitamin E four times

a day. Other vitamins may also be given. A larger intake, especially of

niacinamide or niacin may be prescribed; the usual amount seems to be

about 8 gm. a day after an initial period on 4 gm. a day.

 

The vitamins, as nutrients or medicaments, pose an interesting question.

The question is not, Do we need them? We know that we do need them, in

small amounts, to stay alive. The Teal question is, What daily amounts

of the various vitamins will lead to the best of health, both physical

and mental? This question has been largely ignored by medical and

nutritional authorities.

 

Let us consider schizophrenia, Osmond (19) stated that about 40 percent

of schizophrenics hospitalized for the first time are treated

successfully by conventional methods in that they are released and not

hospitalized a second time. The conventional treatment fails for about

60 percent in that the patient is not released or is hospitalized again.

Conventional treatment includes a decision about vitamin intake. Usually

it is decided that the vitamins in the food will suffice or that a

multivitamin tablet will also be given. The amounts of ascorbic acid,

niacin pyridoxine, and vitamin E may be approximately the daily

allowances recommended by the Food and Nutrition Board of the U.S.

National Academy of Sciences-National Research Council: 60 mg. of

ascorbic acid, 20 mg of niacin 2 mg. of pyridoxine, and 15 I.U. of

vitamin E. Is this amount of vitamins correct? Would many schizophrenic

patients respond to their treatment better if the decision were made

that they should receive 10 or 100 or 500 times as much of some

vitamins? What is the optimum intake for these patients? I believe there

is much evidence that the optimum intake for schizophrenic patients is

much larger than the recommended daily allowances. By the use of

orthomolecular methods in addition to the conventional treatment of

schizophrenia, the fraction of patients hospitalized for the first time

in whom the disease is controlled may be increased from about 40 percent

to about 80 percent. (19)

 

Ascorbic Acid

It was reported by Horwitt in 1942 (20) and by later investigators that

schizophrenic patients receiving the usual dietary amounts of ascorbic

acid had lower concentrations of ascorbic acid in the blood than people

in good health. The loading-test results of VanderKamp (8), Herjanic and

Moss-Herjanic (9), and Pauling and associates (10) have been mentioned

above. In his discussion of ascorbic acid and schizophrenia Herjanic

(21) concluded:

 

The individual variation of the need for ascorbic acid may turn out to

be one of the contributing factors in the development of the illness.

Ascorbic acid is an important substance necessary for optimum

functioning of many organs. If we desire, in the treatment of mental

illness, to provide the " optimum molecular environment, " especially the

optimum concentration of substances normally present in the human body

(Pauling,. 1968 (1)), ascorbic acid should certainly be included (2).

 

There is, moreover, a special reason for an increased intake of ascorbic

acid by patients with schizophrenia or any other disease for which there

is only partial control. About 60 mg. of ascorbic acid a day is enough

to prevent overt manifestations of avitaminosis C (scurvy) in most

people. However, there are several significant arguments to support the

thesis that the optimum intake for most people is 10 to 100 times more

than 60 mg. These arguments are summarized in the papers and books of

Irwin Stone (22) and myself (23,24). They constitute the theoretical

basis for the customary use of about 4 gin. of ascorbic acid a day in

the orthomolecular therapeutic and prophylactic treatment of

schizophrenia. A significant controlled trial of ascorbic acid in

chronic psychiatric patients was reported in 1963 by Milner (25). The

study, which was double-blind, was made with 40 chronic male patients:

34 had schizophrenia, 4 had manic-depressive psychosis, and 2 had

general paresis. Twenty of the patients, selected at random, received 1

gm. of ascorbic acid a day for three weeks; the rest received a placebo.

The patients were checked with the Minnesota Multiphasic Personality

Inventory (MMPI) and the Wittenborn Psychiatric Rating Scales (WPRS)

before and after the trial. Milner concluded that " statistically

significant improvement in the depressive, manic, and paranoid

symptoms-complexes, together with an improvement in overall personality

functioning, was obtained following saturation with ascorbic acid " (25).

He suggested that chronic psychiatric patients would benefit from the

administration of ascorbic acid.

 

We found (10) that of 106 of the schizophrenic patients we studied who

had recently been hospitalized in a private hospital, a

county-university hospital, or a state hospital, 81 (76 percent) were

deficient in ascorbic acid, as shown by the six-hour excretion of less

than 17 percent of an orally administered close. Only 27 of 89 control

subjects (30 percent) showed this deficiency. Great deficiency (less

than 4 percent excreted) was shown by 24 (22 percent) of the

schizophrenic subjects and by only 1 (1 percent) of the controls. I have

no doubt that many schizophrenic patients would benefit from an

increased intake of ascorbic acid. My estimate is that 4 gm. of ascorbic

acid a day, in addition to the conventional treatment, would increase

the fraction of acute schizophrenics in whom the disease is permanently

controlled by about 25 percent, Except for that of Milner (25), no

controlled trial of ascorbic acid in relation to schizophrenia has been

made, so far as I know.

 

Niacin and Niacinamide

The requirement of niacin (nicotinic acid) for proper functioning of the

brain is well known. The psychosis of pellagra, as well as the other

manifestations of this deficiency disease, is prevented by the intake of

a small amount of niacin, about 20 mg. a day. In 1939 Cleckley,

Sydenstricker, and Geeslin (5) reported the successful treatment of 19

patients with severe psychiatric symptoms with niacin and in 1941

Sydenstricker and Cleckley (6) reported similarly successful treatment

of 29 patients with niacin. In both studies, moderately large doses of

niacin, 0.3 to 1.5 gm. a day, were given. None of the patients in these

studies had physical symptoms of pellagra or any other avitammosis. A

decade later, Hoffer and Osmond (2,3) initiated two doubleblind studies

of niacin or niacinamide in the treatment of schizophrenia. Another

double-blind study was reported by Denson in 1962 (26). In 1964 Hoffer

and Osmond (4) reported that a 10-year follow-up evaluation of the

patients in their initial studies showed that 75 percent had not

required hospitalization, compared with 36 percent of the comparison

group, who had not received niacin. Similar estimates have been made by

Hawkins (18). There are, however, contradictory statements by other

investigators. The question of the weight of the evidence is discussed

below in the section on the APA task force report.

 

Pyridoxine

Pyridoxine, vitamin B6 is used in the treatment of schizophrenia in

amounts of 200 to 800 mg. a day by many orthomolecular psychiatrists,

Derivatives of this vitamin are known to be the coenzymes for over 50

enzymes, and the chance of a genotype with need for a large intake of

the vitamin is accordingly great. There is evidence that pyridoxine is

involved in tryptophan-niacin metabolism.

 

A double-blind placebo-controlled study has been made of pyridoxine and

niacin by Ananth, Ban, and Lehmann (27). Their experimental population

consisted of 30 schizophrenic patients: 15 were men, 15 were women,

their mean age was 41.7 years, and their mean duration of

hospitalization was 10.9 years. They were randomly assigned to three

treatment groups: 1) the combined treatment group, which received 3 gm.

of nicotinic acid a day for 48 weeks and 75 mg. of pyridoxine a day

during three 4-week periods; 2) the nicotinic acid group, which received

3 gm. of nicotinic acid a day for 48 weeks and a pyridoxine placebo; and

3) the pyridoxine group, which received 75 mg- of pyridoxine a day

during three 4 week periods and a nicotinic acid placebo. In addition,

neuroleptic preparations were administered according to clinical

requirements for the control of psychopathology. The investigators

reported that " of the ten patients in each treatment group, seven

improved and three deteriorated in the nicotinic acid group, nine

improved and one deteriorated in both the combined treatment group and

in the pyridoxine group " (27). They also stated:

 

Of the three indices of therapeutic effects, global improvement in

psychopathology (Brief Psychiatric Rating Scale and Nurses Observation

Scale for Inpatient -Evaluation) scores was seen in all three groups:

the number of days of hospitalization during the period of the clinical

study was lower in both the nicotinic acid and the combined treatment

group; and only in the combined treatment group was the daffy average

dosage of phenothiazine medication decreased. Thus, improvement in all

three indices was noted in the combined treatment group. However,

several side effects were observed during the therapeutic trials,

indicating that the vitamins used are not completely safe (27).

 

The investigators reached the conclusion that " on balance, these results

suggest that the addition of pyridoxine may potentiate the action of

nicotinic acid. Thus pyridoxine seems to be a useful adjunct to

nicotinic acid therapy " (27). Hawkins (18) commented on this work in the

following way:

 

The therapeutic effect was demonstrable even though the patients had

been hospitalized for an average of 10.9 years, were not on hypoglycemic

diets, and the doses of both pyridoxine (75 mg. daily) and vitamin B3 (3

gm. a day) were considerably below the dosages we routinely prescribe (18).

 

Cyanocobalamin

A deficiency in cyanocobalamin (vitamin B12), whatever its cause, leads

to mental illness as well as to such physical manifestations as anemia.

The anemia can be controlled by a large intake of folic acid, but the

mental illness and neurological damage cannot. A pathologically low

concentration of cyanocobalamin in the blood serum has been reported to

occur in a much larger percentage of patients with mental illness than

in the general population. Edwin and associates (28) determined the

amount of vitamin B12 in the serum of every patient over 30 years old

admitted to a mental hospital in Norway during a period of one year. Of

the 396 patients, 61 (15-4 percent) had a subnormal or pathologically

low concentration of vitamin B 12, less than 150 pg. per ml. (the normal

range is 150 to 1,300 pg. per ml.). This incidence is 30 times as great

as that estimated for the population as a whole. Other investigators

have reported similar results and have suggested that a low serum

concentration of vitamin B12, whatever its origin, may cause mental

illness. In addition, of course, mental illness may accompany some

genetic diseases, such as methylmalonic aciduria, which can be

controlled only by achieving a serum concentration of cyanocobalamin far

greater than normal.

 

Minerals and Other Vitamins

There is some evidence that mental illness may result from deprivation

of or abnormal need for minerals and other vitamins. (See, for example,

Pfeiffer, Iliev, and Goldstein (29)). Further work in this field by

psychiatrists and biochemists is needed.

 

The APA Task Force Report

In July 1973 an APA task force of five physicians and one consultant

issued a 54-page report titled Megavitamin and Orthomolecular Therapy in

Psychiatry (30). In this report the Task Force on Vitamin Therapy in

Psychiatry purports to present both theoretical and empirical reasons

for completely rejecting the basic concept of orthomolecular psychiatry,

which is the achievement and preservation of good mental health by the

provision of the optimum molecular environment for the mind, especially

the optimum concentrations of substances normally present in the human

body.

 

Some Errors in the Report

It is mentioned in the report that in the treatment program of the

orthomolecular psychiatrists " each patient may receive as many as six

vitamins in large doses individually determined by the treating

physician as well as other psychotropic drugs and hormones whose doses

are also individually determined for each patient " (p. 46). The

assumption is made by the task force that the optimum intake of vitamins

for mental health is the conventional average daily nutritional

requirement, with growth and development as the criteria: " In

schizophrenia there is apparently an adequate vitamin intake for growth

and development until the illness becomes manifest in the teens or early

adult life " (p. 40). Mention is made in the report of the well-known

genetic diseases with both psychic and somatic manifestations that can

be controlled by an intake of a vitamin 100 or 1,000 times the usually

recommended daily allowance, but the possibility that less obvious

genetic differences could result in an increased individual need for a

larger intake of vitamins in order to achieve good mental health, as

discussed in my 1968 publication (1) and in the earlier sections of this

paper, is rejected on the basis of arguments that have little value or

pertinence. One such argument is the following:

 

The two theoretical bases adduced by megavitamin proponents for the

effectiveness of NA therapy (nicotinic acid as a methyl acceptor and NAD

deficiency) are in fact generally incompatible, because NAA

[nicotinamide], when functioning as a vitamin, is bound to the remainder

of the coenzyme molecule by the nitrogen of its pyridine ring and hence

can no longer accept methyl groups. Essentially, then, the two views of

NA as a vitamin precursor of NAD and as a methyl acceptor are

incompatible, except for the possibility that there is in schizophrenia

double deficit - both a vitamin deficiency and a transmethylation defect

and that nicotinic acid has the happy fortune to serve two purposes

simultaneously (pp. 40-42).

 

There is an obvious error in this task force argument. There is no

incompatibility between two functions of nicotinic acid; some molecules

may engage in one function and others in the other. A defect in either

function might be controlled by increasing the intake of the vital

substance. A " double deficit " is not needed. The authors of the report

would have won the fallacy in their argument if they had set up some

equilibrium and reaction rate equations, as was done in my 1968 paper

(1). The task force expresses an interesting misunderstanding of the

nature of vitamins, in the following words: " By common definition a

vitamin is not only an essential nutrient, but it is essential because

it is transformed into a coenzyme vital for metabolic reactions " (p.

41). In fact, this is not the common definition of a vitamin; it is

wrong. Some vitamins, including vitamin C, are not known to be

transformed into a coenzyme. This misunderstanding by the task force may

have contributed to the misinterpretation of the evidence for and the

theoretical basis of orthomolecular psychiatry. Nicotinic acid as a

methyl acceptor is referred to in the report: " From Study No. 12:

nicotinic acid in the dosage of 3000 mg. per day can neither prevent nor

counteract the psychopathology induced by the combined administration of

a monoamine oxidase inhibitor (tranylcypromine) and methionine " (p. 16).

In fact, the molecular weights of nicotinic acid and methionine (a

methyl donor) are nearly the same, 123 and 149, respectively. Instead of

3 gm., 16.5 gm. of nicotinic acid would have had to be given each day to

accept the methyl groups donated by the 20 gm. of methionine that was

given each day. The study referred to as number 12 (31), which resulted

in an exacerbation of the illness of 30 schizophrenic patients who

participated in it, has no value as a test of the methyl acceptor theory

of nicotinic acid. Consideration of ethical principles may have kept the

investigators from repeating the study with use of the proper equimolar

amounts of nicotinic acid and methionine.

 

The Failure To Discuss Ascorbic Acid and Pyridoxine

In several places the APA task force report mentions the use of 1 to 30

gm. of ascorbic acid a day by orthomolecular psychiatrists. There are,

however, no references to the literature. Milner's double-blind study

(25) is not mentioned, nor is there any discussion of the many papers in

which a low level of ascorbic acid in the blood of schizophrenics was

reported. Neither the general theory of orthomolecular psychiatry, as

presented in my 1968 paper (1) nor any of the special arguments about

the value of ascorbic acid is presented or discussed in any significant

way. There is, moreover, no discussion in the report of pyridoxine and

no reference to the 1973 work by Ananth, Ban, and Lehmann (27) on the

potentiation by pyridoxine of the effectiveness of niacin in controlling

chronic schizophrenia. The title of the report, Megavitamin and

Orthomolecular Therapy in Psychiatry, is completely inappropriate, and

the general condemnation of megavitamin and orthomolecular therapy is

unjustified.

 

Niacin

The report does my that it is possible that the other watersoluble

vitamins will prove to be more effective than niacin but it adds;

 

Nonetheless, the massive use of niacin has always been the cornerstone

of the theory and practice of megavitamin advocates. Since this has

proved to have no value when is it employed as the sole variable along

with conventional treatments of schizophrenia, the burden of proof for

the complex and highly individualized programs now advocated would

appear to be on the proponents of such treatment (p. 46).

 

I shall point out below that the principles of medical ethics prevent

orthomolecular psychiatrists from withholding from half of their

patients a treatment that they consider to be valuable. Controlled tests

can be carried out only by skeptics. I now ask whether the task force is

justified in saying that the massive use of niacin has been proved to

have no value when it is employed as the sole variable along with

conventional treatments of schizophrenia. My answer to this question,

from a study of the evidence quoted in the report, is that it is not

justified. The evidence that niacin has no value is far from conclusive.

A beneficial effect of niacin or niacinamide was reported for three

double-blind studies (two by Hoffer and Osmond and their collaborators

(2,3,32) and one by Denson (26)) and in 12 open clinical trials by other

investigators referred to in the report. On the other hand, the report

mentions 7 doubleblind studies in which a statistically significant

difference between the niacinamide subjects and the controls was not

observed.

 

A failure to reject with statistical significance the nun hypothesis

that the treatment and the placebo have equal value is not proof that

the treatment has no value. The explicit statistical analysis of an

alternative hypothesis should be carried out: for example, the

hypothesis that there is a 10-percent or 20-percent greater improvement

in the treated subjects than in the placebo subjects. No such analysis

has been published. In fact, some of the " negative " studies indicate

that the treatment has value. The report states that " Greenbaum (33)

reported a double-blind study of 57 schizophrenic children who received

nicotinamide 1 gm. per 50 lbs of body weight or placebo for six months.

No statistically significant differences were seen in the two groups as

a result of the treatment " (P. 11). it is true that no statistically

significant differences were wen, but that is not the whole truth, The

principal criterion of improvement in this study was the increase in the

score on a clinical scale of observable behavior categories. The average

improvement in the score of the 17 children receiving niacinamide was

4.0 units and that of the 24 controls was 2.6 units (there was a third

group of 16 children who were given a tranquilizer and niacinamide). The

children who were given niacinamide showed a 54-percent greater

improvement than the children who were given placebo. The groups were

too small, however, for the difference to be significant at the

95-percent level of confidence. This study does not prove that

niacinamide has no value. Rather, it indicates that niacinamide has

greater value than the placebo, even though it fails to show this at the

customary level of statistical significance.

 

The Hoffer-Osmond Diagnostic Test

Two-thirds of the report relates to niacin and one-third to the

Hoffer-Osmond Diagnostic Test (HOD) (34), which has no special

connection with megavitamin or orthomolecular psychiatry except that it

was devised by the originators of niacin therapy. The report should have

been given the- title Niacin Therapy and the HOD Test, or published as

two reports, one on niacin and one on the HOD test. It would have been

still better for the task force to have discussed megavitamin and

orthomolecular therapy in psychiatry fully.

 

The Question of Controlled Experiments

The report refers to the low credibility of the megavitamin proponents,

whose published results were not duplicated in studies carried out by

one of the task force members (p. 48). The penultimate sentence of the

report is, " Their credibility is further diminished by the consistent

refusal over the past decade to perform controlled experiments and to

report their new results in a scientifically acceptable fashion " (p.

48). I have talked with the leading orthomolecular psychiatrists and

have found that they feel the principles of medical ethics prevent them

from carrying out controlled clinical tests, with half of their patients

receiving orthomolecular therapy in addition to the conventional

treatment and the other half receiving only the conventional treatment.

It is the duty of the physician to give to every one of his patients the

treatment that in his best judgment will be of the greatest value, Some

psychiatrists, including Hoffer and Osmond, carried out controlled

trials 20 years ago. They became convinced that orthomolecular therapy,

along with conventional treatment, was beneficial to almost every

patient. From that time on their ethical principles have required that

they give this treatment and not withhold it from half of their

patients. The task force is wrong in criticizing the orthomolecular

psychiatrists for not having carried out controlled clinical trials

during the last few years. Instead, it is the critics, who doubt the

value of orthomolecular methods, who are at fault in not having carried

out well-designed clinical tests. It is also the duty of a physician to

give to a patient a treatment that may benefit him and is known not to

be harmful. The incidences of toxicity and other serious side effects of

the doses of vitamins used in orthomolecular medicine are low. There is

significant evidence that an increased intake of certain vitamins may

benefit the patient. It is accordingly the duty of the psychiatrist to

prescribe these vitamins for him.

 

The Bias of the Task Force

The last sentence of the report reads as follows:

 

Under these circumstances this Task Force considers the massive

publicity which they promulgate via radio, the lay press and popular

books, using catch phrases which are really misnomers like " megavitamin

therapy " and " orthomolecular treatment, " to be deplorable (p. 48).

 

This sentence, like others in the report, shows the presumably

unconscious bias of the task force. " Promulgate " (misused here) is a

pejorative word, and " catch phrases " is a pejorative expression. I do

not understand why megavitamin therapy and orthomolecular treatment

should be called misnomers. This concluding sentence, like many others

in the book, seems to me to have been written in order to exert an

unjustifiably unfavorable influence on the readers of the report. I have

written two popular books, No More War! (35) and Vitamin C and the

Common Cold (24). I feel that each of them was worthwhile and that

neither would have been easily replaced by a more technical book. The

second book (24) was written because I had discovered in reading the

medical literature that there was much evidence there about the value of

ascorbic acid in decreasing both the incidence and the severity of the

common cold and that this evidence had been suppressed or misrepresented

by the medical and nutritional authorities. Since publication of the

book, eight new studies have been reported. Every one of these has

verified the value of ascorbic acid. The APA report shows the same sort

of negative attitude as that shown by the authorities toward ascorbic

acid in relation to the common cold. There seems to be a sort of

professional inertia that hinders progress.

 

Conclusions

Orthomolecular psychiatry is the achievement and preservation of good

mental health by the provision of the optimum molecular environment for

the mind, especially the optimum concentrations of substances normally

present in the human body, such as the vitamins. There is evidence that

an increased intake of some vitamins, including ascorbic acid, niacin

pyridoxine, and cyanocobalamin, is useful in treating schizophrenia, and

this treatment has a sound theoretical basis. The APA task force report

Megavitamin and Orthomolecular Therapy in Psychiatry discusses vitamins

in a very limited way (niacin only) and deals with only one or two

aspects of the theory. Its arguments are in part faulty and its

conclusions are unjustified.

 

-Based on a lecture given at a meeting of the American College of

Neuropsychopharmacology, Palm Springs, Calif., Dec 47 7 1973 . Reprinted

with permission: Am J. Psychiatry, 131:11, November 1974. Copyright 1974

American Psychiatric Association.

 

References

 

1.Pauling, L.: Orthomolecular psychiatry. Science 160: 265-271, 1968

 

2.Hoffer, A.: Niacin Therapy in Schizophrenia. Springfield, Ill.,

Charles C. Thomas, 1962

 

3.Osmond, H., Hoffer A.: Massive niacin treatment in schizophrenia:

review of a nine-year study. Lancet 1:316-319, 1962

 

4.Hoffer, A., Osmond H.: Treatment of schizophrenia with nicotinic acid:

a ten-year follow-up. Acta Psychiatr Scand 40:171-189, 1964

 

5.Cleckley, H.M., Sydenstricker, V,P., Geeslin, LE-: Nicotinic acid in

treatment of atypical psychotic states associated with malnutrition.

JAMA 112:2107-2110, 1939

 

6.Sydenstricker, V.P., Cleckley, H.M.: The effect of nicotinic acid in

stupor, lethargy and various other psychiatric disorders. Am I

Psychiatry 98:83-92,1941

 

7.Kubala, A.L., Katz, M.M.: Nutritional factors in psychological test

behavior. J Genet Psychol 96:343-352, 1960

 

8.VanderKamp, H: A: biochemical abnormality in schizophrenia involving

ascorbic acid- Int J Neuropsychiatry 2:204206, 1966

 

9.Herjanic, M., Moss-Herjanic, B.L. Ascorbic acid test in psychiatric

patients. J Schizophrenia 1: 257-260, 1967

 

10.Pauling, L., Robinson, A.B_ Oxley S.S., et a]: Results of a loading

test of ascorbic acid, niacinamide, and pyridoxine in schizophrenic

subjects and controls, in

Orthomolecular Psychiatry: Treatment of Schizophrenia. Edited by

Hawkins, D., Pauling, L San Francisco, W.H. Freeman and Co., 1973, pp 18-34

 

11. Orsenberg, LE., Lilljeqvist, A.C., Hsia, Y.E.: Methylmalonic

aciduria: metabolic block localization and vitamin B12 dependency.

Science 162: 805-807, 1968

 

12. Lindblad, B., Olin, P., Svanberg, B., et al: Methylmalonic acidemia.

Acta Paediatr Scand.57: 417-424, 1968

 

13.Walker, F.A., Agarwal, A.B., Singh, R.; Methylmalonic aciduria:

response to oral B12 therapy. I Pediatr 75:344, 1969

 

14.Rosenberg, LE,, Lilljeqvist, A.C., Hsia, Y.E., et al: Vitamin B12

dependent methylmalonicaciduria: defective B12 metabolism in cultured

fibroblasts. Biochem Biophys Res Commun 37:607-614,1969

 

15.Williams, R.J.: Biochemical Individuality. New York, John Wiley &

Sons, 1957

 

16.Pauling, L., Itano, ILA., Singer, S.J., et al: Sickle cell anemia a

molecular disease. Science I 10: 543-548, 1949

 

17.Hawkins, D., Pauling, L (eds): Orthomolecular Psychiatry; Treatment

of Schizophrenia. San Francisco, W.H. Freeman and Co., 1973

 

18.Hawkins, D.: Orthomolecular psychiatry: treatment of schizophrenia.

Ibid, pp. 631-673

 

19.Osmond, H.: The background to the niacin treatment. Ibid,pp. 194-201

 

20.Horwitt, M.K.: Ascorbic acid requirements of individuals in a large

institution. Proc Soc Exp, Biol Med 49:248-250, 1942

 

21.Herjanic, M.: Ascorbic acid and schizophrenia, in Orthomolecular

Psychiatry; Treatment of Schizophrenia. Edited by Hawkins, D., Pauling,

L San Francisco, W.H.

Freeman and Co., 1973, pp. 303-315

 

22.Stone, L: The Healing Factor: Vitamin C Against Disease. New York.

Grosset and Dunlap, 1972

 

23.Pauling, L: Evolution and the need for ascorbic acid. Proc Natl Acad

Sci USA 67:1643-1648, 1970

 

24.Pauling, L: Vitamin C and the Common Cold. San Francisco. W.H.

Freeman and Co. 1970

 

25.Milner, G.: Ascorbic acid in chronic psychiatric patients: a

controlled trial- Br I Psychiatry 109:294-299, 1963

 

26.Denson, R.: Nicotinamide in the treatment of schizophrenia. Dis Nerv

Syst 23:167-172, 1962

 

27.Ananth, J.V., Ban, T.A., Lehmann, H.E.: Potentiation of therapeutic

effects of nicotinic acid by pyridoxine in chronic schizophrenic & Can

Psychiatr Assoc J 18:377-382, 1973

 

28.Edwin, I., Holten, K., Norum, K.R., et al: Vitamin B12

hypovitaminosis in mental diseases. Acta Med Scand 177:689-699, 1965

 

29. Pfeiffer, C.C., Iliev, V., Goldstein, L: Blood histamine, basophil

counts, and trace elements in the schizophrenias, in Orthomolecular

Psychiatry: Treatment of Schizophrenia. Edited by Hawkins, D., Panting,

L San Francisco. W.H. Freeman and Co. 1973. pp. 463-510

 

30. Task Force Report 7: Megavitamin and Orthomolecular Therapy in

Psychiatry. Washington, DC, American Psychiatric Association, 1973

 

31.Ananth, J.V., Ban, T.A., Lehmann, ILE., et al: Nicotinic acid in the

prevention and treatment of methionine-induced exacerbation of

psychopathology in schizophrenics. Can Psychiatr Assoc J 15:15-20, 1970

 

32. Hoffer, A., Osmond, H., Callbeck, J.M., et al: Treatment of

schizophrenia with nicotinic acid and nicotinamide. J Clin Exp

Psychopathol 18:131-158. 1957

 

33.Greenbaum, G.H.C.; An evaluation of niacinamide in the treatment of

childhood schizophrenia. Am J Psychiatry 127:89-93, 1970

 

34.Kelm, H.: The Hoffer-Osmond Diagnostic Test (HOD), in 'Orthomolecular

Psychiatry: Treatment of Schizophrenia. Edited by Hawkins, D., Panting,

L San Francisco. W.H. Freeman and Co. 1973, pp. 327-341

 

35.Pauling, L: No More War! New York. Dodd, Mead and Co. 1958

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