12/7/2021 Gaston Naessens: Somatids, Somatoscope, & 714X; Alternative cancer treatment; Articles & 2 Patents

rexresearch.com

Gaston NAESSENS
Somatids, The Somatoscope, & 714X
( Trimethylaminohydroxybicycloheptane Chloride )

Contact:

Centre d'Orthobiologie Somatidienne de l'Estrie (C.O.S.E.),

5270 Mills St., Rock Forest, PQ, J1N 3B6: 1-819-564-7883;
1-819-564-0492
Cliniques Santé Levesque Clinic, 526 Boulevard du Séminaire
Nord, Suite 202, St. Jean-sur-
Richelieu, Quebec, J3B 5L6, for a
5-day training program in the use of 714X: 1-514-348-4305
Emergency Drug Release Program, Health Protection Branch,
Ottawa: For Canadian physicians
only: 1-613-941-2108

http://www.bccancer.bc.ca/PPI/UnconventionalTherapies/GastonNaessens714X.htm

BC Cancer Agency Cancer Information Centre. (BCCA Cancer

Information Centre search file
2400)

Gaston Naessens (714X)

The role of your cancer health professional is to create an
environment of openness and trust, and to
help in making
informed decisions about alternative/complementary therapies.
Collaboration will
improve the safe integration of all therapies
during your experience with cancer. The "Summary"
and
"Professional Evaluation / Critique" sections of this
Unconventional manual are cited directly

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12/7/2021 Gaston Naessens: Somatids, Somatoscope, & 714X; Alternative cancer treatment; Articles & 2 Patents

from the medical

literature, and are intended to help in the objective evaluation
of
alternative/complementary therapies.

Summary

"Its formulation and administration are based on unconventional

views about the nature of cancer
that have not been
substantiated by mainstream researchers. Side effects appear to
be minimal, but
evidence of its effectiveness is limited."
(Kaegi)

Description / Source / Components

"714-X is the name given to an alternative product developed by

Gaston Naessens, a French
microbiologist now residing in Quebec,
Canada." (Cassileth)

714X contains "a mixture of camphor, ammonium chloride and

nitrate, sodium chloride, ethanol,
and water." (Health)

"Camphor is a natural product derived from the shrub Cinnamomum

camphora." (Kaegi)

714X is injected daily (perinodular). A series of shots

consists of twenty-one daily injections; three
such series are
the minimum required, but most patients should expect to undergo
longer-term
treatment." (Fink 1997)

714X must be "injected intralymphatically via a lymph node in

the groin." (Davies)

This product may be requested by physicians on compassionate

plea under the Emergency Drug
Release Program. The authorization
only provides legal access to the drug and does not ensure or
imply approval of the quality, manufacturing process or clinical
use. (Health) (714X)

"Outside Canada, 714-X is available in Mexico and Western

Europe but not in the US, where it is
currently under
investigation by the Food and Drug Administration." (Kaegi)

History

Naessens claims to have developed in the 1940s "an extremely

powerful light microscope (it uses
ultraviolet and laser
technology) that is capable of extraordinary rates of
magnification -- up to
30,000X -- and can examine living
tissue." (Davies)

"(The later development of the electron microscope, which

allows even higher magnification
[although not of fresh,
unstained blood and tissues], displaced interest in the
somatoscope and other
similar microscopes that used dark-field
microscopy.)" (Kaegi)

Gaston Naessens "was arrested in Quebec in 1989 and charged

with four counts of illegal practice
of medicine and one count
of contributing to the death of a patient." (Roberts)

"Naessens had been convicted four times of practicing medicine

without a license, twice in France,
and twice in Canada."
(Blackburn)

"The name `714-X' reflects Naessens' pride in his creation. The

numbers `7' and `14' represent the
seventh and fourteenth
letters in the alphabet (Naessens' initials), and the `X', the
24th letter in the
alphabet, represents the year of his birth
(1924)." (Kaegi)

Proponent / Advocate Claims

"Gaston Naessens hypothesizes that all living beings, animal

and vegetable, possess life by virtue of
microscopic dense
particles that he calls 'somatids'. His unique approach to
studying morphological
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correlates of health from blood samples

relies on using his Somatoscope and Ultramicroscope to
view the
abnormal cycle of the somatids in the blood (orthodox medicine
has no live blood test for
cancer). ... The centre [Cose Inc.]
believes that cancer development is related to a lowering of
inhibitors (e.g. chalones) transported in the blood." (Fink
1997)

"He [Naessens] believed somatids to be living organisms

distinct from bacteria and viruses, and he
described 2 distinct
life cycles for these organisms: a 'microcycle' consisting of 3
forms, which he
observed in healthy individuals, and a more
complex 'macrocycle' consisting of 16 forms which he
usually
observed in individuals with degenerative diseases, including
cancer. He reports that at the
different stages of the cycle,
the form of the somatids may resemble bacteria, yeasts or fungi.
He
claims to be able to diagnose and monitor disease processes
by observing the number and forms of
somatids in the blood."
(Kaegi)

Naessens believed that "if the somatids are exposed to some

sort of trauma (e.g. pollution,
radiation), then they enter a
wild uncontrolled growth cycle which leads to cancer." The 714X
is
supposed to return the somatids to a normal state. (714X)

"He used the somatoscope routinely to determine whether

treatment with 714-X, a mixture of
nitrogen and camphor (to
deliver the nitrogen), was working for each particular patient.
Naessens
theorized that cancer cells are deficient in nitrogen,
and that injecting 714-X into the lymph system
would convert
them to normal cells." (Cassileth)

"The goal is to fluidify the lymph, and to direct nitrogen to

the cancerous cells in order to stop their
toxic secretions,
which block the organism's defense mechanism." (Fink 1997)

"Naessens selected camphor as the base because he believes it

has special affinity for cancer cells.
... Naessens included
ammonium salts because he believes they improve the circulation
of lymph in
cancer patients. He also believes that the ammonium
salts activate certain kinins that inhibit
abnormal cell growth
and enhance the healthy functioning of the immune system."
(Kaegi)

Proponents believe that "714X acts to strengthen, or unblock,

the dysfunctional immune system."
(Bird)

"Dr. Naessens discovered that tumor cells produce a substance,

cocancerogenic K factor (CKF),
which paralyzes the immune
system. 714X seems to neutralize CKF, thereby enabling the
immune
system to more readily identify and destroy cancer
cells." (Diamond)

"Recently, the distributors have advised that 714-X can

sometimes be administered nasally using a
nebulizer containing a
solution of 0.6 mL of 714-X in 1.9 mL of saline. The nasal route
has been
recommended for patients with lung or oral cancers."
(Kaegi)

"Dr. Atkins cautions that patients undergoing the 714X

treatment should not take therapeutic doses
of vitamin E or
vitamin B12 at the same time, as the two vitamin supplements may
interfere with its
therapeutic action." (Diamond)

Professional Evaluation / Critique

"There is no scientific evidence in support of the efficacy of

this method." (Cassileth)

"Naessens's theories about the underlying causes and mechanisms

of cancer are clearly not
consistent with current scientific
opinion. Although a small number of researchers have long
believed that certain bacteria, viruses and other organisms such
as cell-wall deficient or pleomorphic
bacteria play a much more
important role in the development of cancer, this view is not
generally
accepted by mainstream scientists." (Kaegi)

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"There have been few published animal studies of the safety and
effectiveness of 714-X, and those
that have been conducted have
shown no beneficial effect." (Kaegi)

"It is safe to say that the 'microscope invention' is a

hodge-podge of different physics phenomena,
which either are
non-existent and certainly cannot be demonstrated to exist in
any laboratory of a
reputable university or any other similar
institution (e.g. two wavelengths combining to produce a
third
wavelength), or a known physics phenomena which do exist (e.g.
Zeeman effect) but do not
act at all as described by this man.
If the rest of his "discoveries" in any way resemble the
microscope 'discovery', then I must conclude that his whole
theory of somatids and immune system
booster compound 714-X and
their role in cancer diagnosis and treatment has no value."
(Palcic)

"A few animal studies using extracts of the shrub C. camphora,

which is the natural source of
camphor, have demonstrated some
evidence of biological activity of potential value in the
treatment
of cancer. ... However, research into the effects of
camphor remains at an early stage." (Kaegi)

Toxicity / Risks

714X has no (reported) side effects but should be used only

with the supervision of a physician.
(Fink 1988)

The administration is complex. 714X must be given

intra-lymphatically into a lymph node in the
groin every day for
21 days. The container vial is expected to be used for several
treatments and no
information on preservatives or stability of
714X given. Vials must be stored in the refrigerator.
(Nakashima)

"714X has no harmful side effects, other than burning

sensations at or around the site of injection."
(Diamond)

"Taken internally, camphor may have serious toxic effects."

(Kaegi)

Costs

A series of injections cost approximately $350 Cdn. (Ontario,

1994)

It costs $320 U.S. for one series of shots consisting of 21

daily injections. Included with the
medicine are a protocol,
injection instructions, and a videocassette on the treatment.
(Fink 1997)

In Canada, 714X is reported to cost $69.55 for 2 vials of 5 mL

in 1993. (Nakashima, 1996)

References

Bird C. Gaston Naessens vs. scientific medicine. Townsend

Letter for Doctors 1991 May;94:313-
320.

Blackburn L. Methods detect cancer, Branigan insists. The

Whitehorse Star. (BCCA Cancer
Information Centre search file
2400)

Cassileth BR. Alternative medicine handbook: the complete

reference guide to alternative and
complementary therapies. New
York: W.W.Norton & Co., 1998:165-6.

Davies R. The story of Gaston Naessens. Shared Vision 1991

June:16-17,39.

Diamond WJ, et al. An alternative medicine definitive guide to

cancer. Tiburon: Future Medicine
Publishing, Inc., 1997:32,871.

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12/7/2021 Gaston Naessens: Somatids, Somatoscope, & 714X; Alternative cancer treatment; Articles & 2 Patents

Fink JM. Third Opinion: an international directory to

alternative therapy centers for the treatment
and prevention of
cancer and other degenerative diseases. 2nd ed. Garden City
Park, New York:
Avery Publishing Group Inc., 1988:47.

Fink JM. Third opinion: an international directory to

alternative therapy centers for the treatment
and prevention of
cancer and other degenerative diseases. 3rd ed. Garden City
Park, New York:
Avery Publishing Group Inc., 1997:67.

Health Protection Branch. 714-X: an unproven product. Issues

(Canada Health Protection Branch)
1990 Jan 24.

Kaegi E, on behalf of the Task Force on Alternative Therapies

of the Canadian Breast Cancer
Research Initiative.
Unconventional therapies to cancer: 6. 714-X. Canadian Medical
Association
1998;158:1621-1624.

Nakashima L. BC Cancer Agency verbal communication 1996.

Ontario Breast Cancer Information Exchange Project. Guide to

unconventional cancer therapies. 1st
ed. Toronto: Ontario Breast
Cancer Information Exchange Project, 1994:250-252.

Palcic B. Naessens' somatoscope. BC Cancer Agency Vancouver

Cancer Centre Cancer Information
Centre.

Roberts PW. Blood Feud. 1992 Dec: 52-57, 96-105.

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714X
( Trimethylaminohydroxybicycloheptane Chloride )

714X is manufactured by the private laboratory Centre

expérimental de recherches biologiques de
l'Estrie Inc.
(C.E.R.B.E. inc.).  The product is exclusively distributed
by CERBE Distribution Inc.
and its authorized agents.

714X developed for perinodular injections (basic treatment)

This product is available in 6.5 ml vials. Two vials are

required to complete 21 consecutive days of
treatment referred
to as one cycle. This basic treatment is directly administered
into the large
lymphatic circulation (See Section J).

714X developed for inhalation through the respiratory tract

(secondary treatment, if necessary).

The secondary treatment of 714X is performed with the use of a

medical device known as a
nebulizer. This treatment is added to
reach the smaller segment of the lymph system known as the
small
lymphatic circulation.
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714X contains nitrogen as its primary ingredient, camphor as

its vehicle, mineral salts and 18 trace
elements.

Aluminum  < 0.5 ppm

Antimony  < 1.0 ppm
Arsenic  < 1.0 ppm
Barium  0.7 ppm
Bore  < 0.05 ppm
Cadmium  < 0.05 ppm
Calcium  0.5 ppm
Chromium  < 0.1 ppm
Cobalt  < 1.0 ppm

Copper  0.01 ppm

Iron  < 0.1 ppm
Lead  < 1.0 ppm
Magnesium  6.5 ppm
Mercury  < 1.0 ppm
Molybdenum  < 1.0 ppm
Nickel  < 0.1 ppm
Phosphorus  < 5.0 ppm
Zinc  2.0 ppm

Sodium chloride content (NaCl) was evaluated at 8.2 g/liter.

Summary of the chemical analysis evaluation

* The absence of proteins and immunoglobulins shows that 714X

is not an immune serum prepared
after injection to
animals.  714X is not a vaccine.

* The presence of sodium chloride at a level of 8.2 g/liter

shows that it is an isotonic solution having
a pH=7
(physiological solution).  This solution complies with
norms for injectable solutions of the
pharmaceutical industry.

* The gas chromatography coupled with the mass spectrometry

reveals the presence of camphor or
trimethyl-(1.7.7) bicyclo
(2.2.1.) heptanone-2 that we have quantified.  Its
concentration is 0.09
mg/ml (90 ppm).  A nitrogenated
compound and hydrochloric acid were also detected.

* The test using the camphoroxime that was synthesized shows

that this molecule does not exist as
such in the sample of 714X
analyzed.  The nitrogenated compound could not be clearly
identified
with the testing done.

* Eighteen metals have been measured. They all are at trace

levels, of the order of ppm (parts per
million) and are without
biological significance, except magnesium, whose level of 6.5
ppm is still
with no therapeutic significance. (This is the
opinion of the laboratory. However, the manufacturer
claims that
the trace levels identified do have a biological significance.)

714X is not designed to destroy diseased cells.

714X is a product created to improve health by revitalizing the

immune system and is not designed
to directly act on disease
related symptoms.

714X supports natural defenses (including the immune system)

when introduced into the lymphatic
circulation.

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The particular method of administration of the product makes it

unique.

A brief overview of the physiology of the lymph system is

necessary given 714X's method of
administration :

Most of the constituting elements of blood plasma flow freely

through the capillary walls to form
the interstitial fluid.
Blood capillaries lose more fluid through filtration than they
recover through
reabsorption. The excess fluid filtered through
the blood system (approximately 3 liters per day)
penetrates the
lymphatic capillaries where it creates the lymph.

The resulting lymph then flows in parallel to the large blood

circulation. The lymph is then
discharged into the venous blood
(that is the blood which brings waste matter to the heart) at
the
junction of the sub-clavicle veins and the internal jugular
veins in the neck area.
The lymphatic system is comprised of the lymph, the lymphatic
vessels in which the lymph flows
and many structures and organs
which contain lymphatic tissue and bone marrow where
lymphocytes
are produced.

The lymphatic system fills several roles :

1. It drains interstitial fluids. The lymphatic vessels drain

any excess interstitial fluids located
between the cells. This
liquid once collected in the lymphatic vessels is called the
lymph.

2. It carries away the digestive fats. The lymphatic vessels

transport the various fats and liposoluble
vitamins absorbed by
the digestive tube.

3. It protects the organism against foreign bodies. The

lymphatic tissue triggers immune responses.
These responses are
specific to bacteria, viruses or immature cells. The lymphocytes
(a type of
white blood cell that creates antibodies) with the
help of macrophages, detect foreign bodies,
microbes, viruses
and immature cells such as cancerous cells.

From an anatomical point of view, nature has provided the body

with a double lymphatic
circulation. These two circulations,
which do not communicate with each other, act in a closed
circuit.  Never touching each other, they nonetheless both
discharge into the blood stream (See
adjoining diagram).

The large lymphatic circulation drains 75 % of the body, being

the lower left and right sides of the
body as well as the upper
left side of the body.

The small lymphatic circulation drains 25 % of the body being

the upper right side of the body.

To access the large lymphatic circulation, 714X must be

introduced by way of perinodular injections
into the right
inguinal area.

To access the small lymphatic circulation, an ultrasonic

nebulizer must be used to allow the nodes
located in the
respiratory tract to absorb 714X .

When introduced into the lymphatic system, 714X acts in three

ways :

1. It liquefies the lymph, meaning that it renders the lymph

more fluid and capable of easier
circulation (better able to
assure draining of cellular toxins).

This fluidifying action of 714X is produced by the sodium and

ammonium chlorides contained in
the product.  A fluidified
lymph can once again insure elimination of toxins and trigger
appropriate
immune responses.

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N.B. : Clinical observations using a lymphograph revealed that

the lymph of a person afflicted with
a degenerative disease is
both thick and stagnant.  It does not flow freely. 
This observation raised
the hypothesis that the lack of fluidity
in the lymph can be a biological precursor to degenerative
diseases.

2. It brings nitrogen to the organism as an active ingredient.

Nitrogen is a fundamental element to
the creation of living
matter : it is also an essential element to cellular
repair.  It is carried to the
blood stream by the lymphatic
circulation.

Where cancer is present (uncontrolled immature cell division)

immature cells reach a critical mass
that requires nitrogen to
develop.  These cells then secrete a substance which
paralyses the immune
system so that they can then get their
required nitrogen from healthy cells.

A vicious cycle then is established which supports the growth

of cancerous cells while the immune
system is unable to act.

By bringing nitrogen to the immature cells, 714X stops the

secretion of the paralyzing factor by the
immature cells thus
allowing the immune system to recover its natural functions.

3. 714X brings 18 trace elements to the system thus promoting

intercellular communications. The
trace elements contained in
714X facilitate inter and intra cellular communications,
necessary
exchanges that may have been temporarily interrupted
or blocked by the progressive clogging up of
a stagnating lymph.

714X acts directly on the lymph to restore its immune activity.

By its direct action on the lymph and its arrival into the
blood stream (once mixed with the lymph),
714X normalizes the
biological functions related to homeostasis. It is a product
which harmonizes
the biochemical reactions involved in normal
cellular development, in tissue repair and in the body's
specific and non-specific defense mechanisms.

714X's therapeutic effects can be summarized in two ways :

1. An increase in the body's natural defense mechanisms, that

is, the non-specific immune defense
mechanisms that act upon
foreign bodies such as bacteria and viruses. Natural defense
mechanisms
include the skin, the mucous membranes, the
anti-microbial chemical reactions, phagocytosis by
neutrophiles,
inflammation and fever mechanisms.

2. An increase in the specific immune responses principally

assured by lymphocytes (B and T) and
macrophages which acting
together detect cells and foreign bodies, germs and cancerous
cells
flowing through the body. These immune responses are
triggered to establish contact with foreign
substances, destroy
them and then eliminate them so that they will not impede the
normal metabolic
functions of the body's organs. 714X thus
allows a weakened organism the opportunity to regain its
defense
mechanisms and therefore enhance the process of cellular repair.

714X is a non-toxic treatment which supports the body's natural

defense mechanisms. It is
compatible with most therapeutic
approaches seeking to bolster the biological terrain. These
therapies are generally referred to as non-conventional,
complimentary, alternative, etc.

Clinical observations have revealed certain exceptions in the

case of :

* Vitamin B-12
* Vitamin E
* Shark and bovine cartilage as well as other antiangiogenic
products.

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These exceptions apply to dietary supplements but do not

include vitamins B-12 and E found in
food.

Vitamin B12

It is recommended not to simultaneously use 714X and vitamin

B12 supplements.

Vitamin B12 accelerates cellular division (especially blood

cells) without distinguishing healthy
cells from immature
cells.  There is nothing to be gained by stimulating cell
division in an already
hyperactive organism.  This
restriction does not affect vitamin B12's properties in a normal
context.

For those persons having had a partial or total removal of the

small intestine who wish to take 714X,
the above exception
concerning vitamin B12 does not apply as this vitamin is
essential for such
persons' survival.

Vitamin E

It is not recommended to use 714X and vitamin E supplements

simultaneously.

It is a recognized fact that vitamin E protects cellular

membranes against free radicals. This
antioxidant property of
vitamin E is important in the prevention of cancer, but once
cancer has taken
hold of the organism, this vitamin could create
a protective coating around immature cells and thus
delay their
identification and elimination by the immune system.

Shark and bovine cartilage

It is not recommended to use 714X and shark or bovine cartilage

or antiangiogenic products
(products aiming at shrinking blood
vessels) simultaneously

Shark cartilage seeks to asphyxiate a tumoral mass by stopping

its vascularisation process. This is a
valid approach if one
considers cancer as a localized problem.

However, if one considers cancer as a generalized disease which

localizes itself in a vulnerable area
of the body, it becomes
useless to act locally if the defense mechanisms are not
supported. In this
approach, the tumor is only confirmation of a
more profound problem.

Shark cartilage is incompatible with 714X as 714X requires a

good blood circulation so that the
body may eliminate tumoral
masses.

714X is not toxic and does not destroy diseased cells. It only
supports the body's natural defense
mechanisms and its immune
system. It can be used with conventional treatments whether they
be
chemotherapy, surgery, radiation therapy or other therapies.
It does not hinder their respective
modes of action nor does it
modify their effectiveness. 714X combined with conventional
therapies
can only benefit the patient as it promotes the
elimination of metabolic waste matter (meaning
toxins) produced
by the above mentioned conventional treatments. It can also
reduce the intensity of
certain side effects associated with
conventional therapies such as nausea, loss of appetite, etc. as
it
helps the body to cleanse itself by favoring the circulation
of the lymph and by assisting in cellular
repair by bringing
nitrogen to the organism.

Manufacturer's recommendation

If surgery is to occur and the patient's life is not in any

immediate danger, it is recommended that a
full 21 consecutive
day course of 714X be done prior to surgery. This procedure can
only assist the
organism by promoting a strong local and
systemic immune response.

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For those cancer patients requiring surgery, the above

recommendation becomes even more
important as it reduces the
risks of spreading cancer to a new site (metastasis), given that
surgery
can assist the migration of cancerous cells via the
lymphatic system.

714X may be used for preventive purposes. In such cases, one to

three consecutive cycles of
perinodular injections are
recommended.

When dealing with a degenerative disease confirmed by a medical

diagnosis, 714X may be used by
itself or in conjunction with
other treatments. In these cases, a minimum of 6 to 8
consecutive cycles
of injections are required. In some cases,
continued use may be necessary even though 714X was
not
conceived as a lifelong medication.

The quantity of product to be injected as well as the frequency

of the injections appears in the
adjacent calendar :

It is pointless to increase daily doses in the hope of speeding

up the healing process. The
recommended dosages have been
clinically determined and remain those having afforded the best
results.

1. Progressive doses are administered during the first five

days of the first cycle beginning with 0.1
ml. on day one, 0.2
ml on day two and so on until day five. This progression is
necessary to avoid
overtaxing the elimination organs due to the
increased number of toxins being eliminated once the
lymph
becomes more fluid.

2. From day five of the cycle to day twenty-one, the daily dose
will be 0.5 ml.

3. Each twenty-one day cycle must be followed by two days with

no injections being performed to
allow the organism to rest.

4. The second and all subsequent cycles will consist of 0.5 ml

injections from day one to day
twenty-one inclusively.

5. Children weighing less than 30 kg (66 pounds) will receive

one half of the daily dose prescribed
for adults but will also
complete full twenty-one day cycles.

Ultrasonic nebulizer treatments

Ultrasonic nebulizer treatments require a special mixture of

714X which has a different molecular
weight than the injectable
product. The nebulizer product is packaged in 2 ml ampoules,
seven
ampoules being included in each box. Three boxes are
required for a 21 day cycle.

The nebulizer treatment is a secondary treatment which begins

only during the second injection
cycle. A 12 hour interval is
required between the injections and the inhalations by way of
the
nebulizer. Some people prefer injecting in the morning while
others prefer the evening. This
depends on each person's
tolerance and routine.  From a biological standpoint, there
is no
difference. It remains a strictly personal choice.

Side effects are generally understood to mean foreseeable and

harmful side effects present amongst
all users. Such effects are
not systematically found in people using 714X.

To the contrary, using 714X can increase the quality of life of

its users (increased vitality and pain
threshold, better
appetite, less stress, etc.). Each person's constitution as well
as their body's need for
cleansing and cellular repair will be
factors influencing how 714X acts upon them. Each person is
different. It is most difficult to gage 714X's impact from one
person to another.

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Occasionally, during the first treatment cycle, certain

observations will confirm that the cellular
cleaning process has
begun. Most users do not notice any particular changes except
for improved
activity in the elimination organs (bladder,
intestines, lungs).

It is recommended however to strictly apply the utilization

protocol of 714X to avoid any
discomforts which may result from
a rapid application of the product.

Conclusion

714X is a health product conceived and manufactured to support

the body's natural defenses. The
method chosen to achieve this
objective is the liquifying of the lymph. Once liquefied, the
lymph
can resume its normal draining functions as well as its
other immunological properties.

714X is easily absorbed by the body : it sustains life by

bringing to the organism fundamental
elements such as nitrogen
(brought to the system by the camphor molecule) and a variety of
trace
elements.

714X is non-toxic. It produces no harmful side effects. It may

be used in a preventive mode. It is
recommended for those people
suffering from some sort of immune deficiency or degenerative
disease confirmed by a medical diagnosis.

The Lymphatic Pathway

US Patent # 6,596,295
Aqueous Solution for Treating Degenerative
or Autoimmune Diseases and/or as an
Immunomodulatory Agent

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22 July 2003
US Cl. 424/422

Gaston NAESSENS

Abstract -- The invention concerns an aqueous solution

capable of being injected by perinodular
delivery or inhaled for
use in the treatment of degenerative or autoimmune diseases or
as
immunomodulatory agent. Said solution is prepared by reacting
camphor on ammonium hydroxide.
The resulting product is then
suspended in a saline solution. Said preparation having a basic
pH is
then neutralized with nitric acid. The resulting aqueous
solution has pharmacological properties
since it is an analogue
of human cytokines, which makes it useful for treating
degenerative or
autoimmune diseases and/or as an
immunomodulatory agent.

Foreign Patent Documents

GB 385,148 (1932) // WO 97 05780

Description

The present invention relates to an aqueous solution that is

administrable by perinodular injection or
by inhalation and is
usable for treating degenerative or autoimmune diseases and/or
as an
immunomodulatory agent.

The invention also relative to a method for preparing this

solution.

This method is characterized in that: in a first step, camphor

is reacted with ammonium hydroxide;
in a second step, the
product obtained in the first step is suspended in an aqueous
solution of sodium
chloride; and in a third step, the pH of the
liquid suspension obtained in the second step is
neutralized
with nitric acid to obtain the desired aqueous solution.

The aqueous solution according to the invention as obtained by

the method described above, has
been thoroughly tested and has
proven to have pharmacological properties which make it
efficient
for the treatment of degenerative or autoimmune
diseases and/or as an immunomodulatory agent.

Thus, it has been noticed that it mimicks human cytokines.

Thus, it acts on monocytes to transform
them into macrophages
which, in turn, secrete two proinflammatory cytokines:
interleukin 1 beta, 6,
8.alpha. and a tumor necrosis factor TNF
alpha. Depending on the mimicked cytokine family,
monocytes are
transformed into macrophages or block molecules which paralyse
the immune
system. In both cases, a stimulation of the immune
system and an increase in the tumor necrosis
factor, which is
also classified among immunostimulating factors, occur. This
factor is also known
for the role it plays in host resistance
against viral infections or others, and in tumor development.

Based on testings performed on animals, the solution according

to the invention would be applicable
in human therapeutics using
0.075 ml per pound of body weight for 21 days, that is to say a
total of
10.5 ml per series, which corresponds to 0.5 ml per day
for a person weighing 140 pounds.
Administration can be done by
perinodular injection or by inhalation with an ultrasonic
nebulizer.

For a person of 140 to 190 pounds, the first series should be

applied in a progressive way according
to the following
schedule:

1.sup.st day 0.1 ml injection 2.sup.nd day 0.2 ml injection

3.sup.rd day 0.3 ml injection 4.sup.th day
0.4 ml injection
5.sup.th day 0.5 ml injection

All the other injections should comprise the same volume (0.5
ml) of injected product.

The following series will use 0.5 ml at each injection for 21

days.

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Cycles can be repeated if needed with an interruption of 2 days

between each cycle.

The structure of the active principle present within the

aqueous solution according to the invention
has not been
established with precision yet. As it stands out on the reaction
diagram identified as
FIG. 1 in appendix, camphor reacts in a
reversible way with ammoniac to produce a hemiaminal
derivative.
This hemiaminal derivative of camphor is itself prone to a
number of possible reversible
conversions in the presence of
ammoniac and water, and has been impossible to identify by
infrared
spectrophotometry yet. However, the Applicant however
thinks that it is the chloride of this
hemiaminal derivative of
camphor obtained in the second step of neutralization which is
probably
the active principle of the aqueous solution insofar as
the structure of this derivative could
effectively mimick the
structure of .beta. family cytokines which are known to act on
monocytes
and stimulate the production of IL-1 beta, 6, 8 and
TNF alpha. The complete chemical name of the
chloride derivative
is the trimethyl-1,7,7 amino-2 hydroxy-2-bicyclo [1,2,2] heptane
chloride.

The invention will be better understood upon reading what will

follow in a practical example of
synthesis and the detailed
description of assays performed up to now by the Applicant.

EXAMPLE

In a container sealed hermetically, 108 mg of camphor (C.sub.10

H.sub.16 O) is added to 0.9 ml of
ethyl alcohol (C.sub.2 H.sub.5
O), until complete dissolution. Then, the alcoholic solution so
obtained is added to 5.2 ml of ammonium hydroxide (NH.sub.4 OH).
The obtained mixture is
shaken.

In another erlenmeyer, 0.9 g of sodium chloride (NaCl) is

dissolved in 79 ml of sterile, non
pyrogenic water. The content
of this other erlenmeyer is added to the mixture previously
prepared.
The new mixture obtained is vigorously shaken.

The so prepared aqueous solution presents a fluffy precipitate

and supernatant. After three days at
room temperature and daily
shaking, the precipitate is completely dissolved.

The aqueous solution is in the form of a clear liquid, with an

ammoniacal smell and an alkaline
flavour, the pH of which is
10.4. Then, the pH is adjusted to 7 by introducing 14.9 ml of
nitric acid
(HNO.sub.3)N.sub.6.

The final solution obtained is then filtered through a

millipore filter of 0.2 micron.

It is obvious that the basic chemical products used and

previously mentioned comply with the U.S.P.
standards and are
manipulated in conditions of total asepsis.

Biological Properties

The biological properties which were obtained with the solution

prepared as described in the
preceding example, are the
following: 1) It acts on monocytes in vitro. 2) It transforms
monocytes
into mature macrophages in vitro. 3) In vitro again,
transformed macrophages are stimulated to
secrete
proinflammatory cytokines. (a) Interleukin-1 beta (IL-1 beta)
known to exert a large variety
of effects on differentiation and
function of cells involved in inflammatory processes and immune
responses; and (b) IL-6, 8 alpha and tumor necrosis factor (TNF
alpha), also classified as an
immunostimulatory agent and known
to play a role in host resistance against infections and tumor
development.

It is known that the cellular immune response is controlled and

modulated by a family of relatively
small molecules called
<<(cytokines)>> which are small protein hormones
playing a role in
numerous normal cell functions. Their
functions encompass anti-tumor, anti-viral and anti-bacterial

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activities and they induce immune cell growth, differentiation,

activation, chemotactism, adhesion
and immunosuppression.

This family of immunomodulators has recently been discovered.

More than 70 different molecules
have been identified but it
seems that the family comprises more than 200 members. In other
words,
to date, cytokines are only partially known and
characterized.

Known cytokines have been divided into two groups, alpha and
beta, based on their structure. Alpha
cytokines include
interleukins, interferons, and other growth factors which
control immune cell
proliferation. Beta cytokines include MIP
(Macrophage Inflammatory Proteins), MCP (Monocyte
Chemoattractant Proteins), RANTES, and other proteins which
attract immune cells toward a site of
infection or a tumor and,
in doing so, strengthen the activity of the immune system. It
seems that
each cytokine molecule is very specific and only
targets a small subpopulation of lymphocytes. In
addition,
cytokine fragments as small as 3 to 7 amino acids can bind to
lymphocytes and partially
mimick or block the activity of a
complete cytokine molecule.

It is also known that the last three amino acids at the

C-terminal end of beta cytokines are nitrogen-
oxygen which bear
a positive charge. It is thus possible that the aqueous solution
according to the
invention could exert a stimulatory effect to
secrete cytokines since, as a result of its preparation, it
may
contain a small amount of nitrogen-oxygen molecules which look
like and mimick the three
amino acid-sequence of the beta
cytokine family. Depending on the required cytokine activity,
the
solution according to the invention can either activate the
transformation of monocytes into active
macrophages or block the
action of other molecules which paralyse the immune system. In
either
case, the result could be reinforcement of the immune
system and the natural defenses to increase
tumor cell
destruction.

Results of the Assays Carried Out

Various assays and tests described thereafter were carried out

with vials filled with the aqueous
solution prepared according
to the example given hereinabove.

1) Control Tests of the Solution

The aqueous solution prepared according to the invention was

tested. In practice, it should be
limpid, clear and volatile,
and leave a dry extract of 63 mg per ml.

2) Sterility Assays

Ten randomly selected vials were incubated at 37 degrees for 48

hours. Then, each vial content was
seeded as follows: a) 1 ml of
solution respectively in two tubes of 60 ml containing
thioglycolate
medium (Difco) and a tube of 60 ml containing
Sabouraud liquid medium (Difco). b) 0.25 ml of
solution
respectively in two tubes of 60 ml containing thioglycolate
medium (Difco) and a tube of
60 ml containing Sabouraud liquid
medium (Difco). c) A thioglycolate tube of group A and a
thioglycolate tube of group B were incubated at 35 degrees for
10 days, all the other tubes being
kept for 10 days at room
temperature (about 20 degrees).

All seeded tubes were maintained sterile.

3) Toxicity Assays

Pharmacological assays performed on healthy animals showed an

absence of toxicity, even at very
high doses.

Then, one was able to intravenously inject 1 ml of product to a

9-pound rabbit, without being in a
position to observe an
unfavourable reaction. In the same way, one was able to inject
0.2 ml of

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product per pound of body weight to cats and 0.3 ml of

product per pound of body weight to dogs
without observing
unfavourable reactions.

By lymphatic delivery, one was able to inject to cats of 10 to

12 pounds up to twice the total dose
prescribed in human
therapeutics, for a body weight of 140 to 190 pounds, without
observing
unfavourable reactions.

4) Therapeutic Assays

The therapeutic activity of the product was observed for almost

three years in 26 cats and 20 dogs
suffering from various
degenerative pathologies as well as viral and bacterial
infections.

Single injected doses varied by one twentieth up to the total

dose proposed above in human
therapeutics.

The therapeutic activity of the product was observable in all

cases right from the second day of
treatment. This activity
presented itself either by regression of tumor or lymph node
masses, or by
resumption to vital functions and return to a
satisfying general state after infectious diseases.

Optimal results were recorded with a posology of 0.075 ml per

pound of body weight, for a 21-day
cycle, which has permitted to
establish the previously mentioned posology applicable to human
therapeutics.

5) Pharmacological Assays

As previously indicated, the aqueous solution according to the

invention acts on neoplastic cells and
prevents them from
secreting a substance which drives leucocytes and other
phagocytic elements of
the organism into a state of negative
chemotactism.

Suppression of this secretion then allows the immune system to

consider the neoplastic formation as
a foreign body and destroy
it. Animal testing showed that elimination of lysed tumor masses
occurs
through emunctories. Cancer cells thus evacuated present
a nuclear disruption making any mitosis
impossible. These
evacuated cells are surrounded by an enormous amount and variety
of very active
leucocytes.

Animal testing also showed that hematological constants in

treated animals reached standard levels
right from the first
week of treatment.

The aqueous solution according to the invention can be used as

such, preferably by lymphatic
delivery.

From a practical point of view, it is worth noting that this

solution can not be exposed to germicidal
tube rays (a 2537
angstrom-ray for example).

714X

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Canada Patent # 2,282,865

DIACHROMIC MICROSCOPE CONDENSER

3-20-2001
Gaston NAESSENS

Classification: - international: G02B21/08; G02B21/18;

G02B21/06; G02B21/18; (IPC1-7):
G02B21/08; - European:
G02B21/08D; G02B21/18

PDF Format

Nexus Magazine (February-March 1994)

The Amazing Wonders of Gaston Naessens ---

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Super-Microscopes and Suppressed Cancer

Treatments
by

Steven Elswick
The landscape of medical science is on the verge of being
radically altered forever by the use of a
powerful microscope
(the Somatoscope) developed by Gaston Naessens of Quebec,
Canada, This
incredible device reaches magnification levels of
20,000 to 30,000 diameters—well above the 2,500
diameter limit
of conventional microscopes. The sheer magnitude of the
difference in performance
gives the appearance of either a gross
violation of the laws of physics, or fraud.

A radical departure in performance from optical and scanning

electron microscopes registers this as
a truly great discovery.
Unfortunately, in most fields of science, a great deal of effort
is put forth
into listing why something will not work instead of
attempting to duplicate the results. This in turn
creates a
situation where what was science, turns into religion where the
orthodox dogma is to be
taken on faith, and that which defies
dogma is to be persecuted as heresy. The inertia of a dogma
slows down the rate new discoveries can be made. In the medical
fields, slow acceptance of new
ideas can cause many needless
deaths. This is the case with the supermicroscope and the
discoveries
of B&hamp, Rife and Naessens.

NOTES

In the 1930s, an obscure and dedicated scientist, Royal Raymond

Rife, had successfully developed
the Universal Microscope which
was able to provide amplification levels of 60,000 times without
killing the specimens! Rife was able to observe live viruses and
their reaction to certain stimuli. His
observation that bacteria
could change into viruses and viruses could change form,
violated the
strongest medical dogma—the germ theory of disease.

In 1934, after learning how to seek out and destroy the

insidious cancer virus, Rife opened a clinic
in which he cured
16 out of 16 patients within three months! Working side by side
with some of the
most respected researchers in America, Rife
treated patients electronically to kill the virus and then
allowed the body's immune system to restore the body to full
health. Many prestigious (and
competent) organisations and
institutions over­saw and verified much of Rife's work during
the
1930s.

Independent physicians using Rife's therapy were treating and

curing as many as 40 patients per
day. Other degenerative
conditions and illnesses such as cataracts, herpes and
tuberculosis were
found reversible and curable with Rife's
equipment This work was described in various medical
journals of
the time as well as the Smithsonian Institution's annual report
and Science magazine.
Unfortunately, Rife's success attracted
the attention and wrath of the American Medical Association
(AMA) and the powerful pharmaceutical companies—the organised
opposition of the medical
fields.

Although Rife's work was in direct conflict with the orthodox

views of his time, he was supported
by many top-rated doctors.
Many of these doctors continued using these devices in secret in
defiance of the AMA and the US government. The carefully
documented records kept by these
brave doctors and testimonials
by their patients vindicate Rife's theories. Many of these case
histories and anecdotes about Rife's treatment can be found in
the book, The Cancer Cure that
Worked! by Barry Lynes.

The fascinating work of Rife was suppressed and he—like Tesla

before him—joined the ranks of
the forgotten inventors of the
early part of this century. It has only been in the past few
years that the
general public has begun to develop an awareness
that there is something wrong in the technical
world.
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MODERN UNIVERSAL MICROSCOPE

What Rife accomplished optically in the 1930s with his

Universal Microscope, Gaston Naessens
accomplished with a
combination of optics and electronics in the 1940s in his
Somatoscope. Born
on 16 March 1924 in Roubaix, France, Gaston
displayed a predisposition to be an inventor when at
the age of
five he built a little moving autolike toy from a Meccano set
and powered it with an alarm
clock spring. Later, he built a
home-made motorcycle and a mini-airplane!

While attending the University of Lille, Gaston nearly had his

education disrupted by the German
invasion. Fortunately, Gaston
and his fellow students escaped to Nice where they carried on
their
education in exile. He was awarded a diploma from the
Union Nationale Scientifique Francaise—a
quasi-official
institution under whose auspices the education of the displaced
students continued. He
did not bother seeking an equivalency
degree from the de Gaulle government when the French rule
was
restored.

At the young age of twenty-one, frustrated by the limitations

of conventional microscopes, Gaston
set out to build a superior
microscope. Technical assistance was provided by German
craftsmen
from Wetzlar, Germany, who checked out many of
Gaston's original ideas on optics. Privately,
Gaston devised the
electrical manipulation of the light source Once the technical
aspects were
resolved, Gaston had the body of his microscope
constructed by Barbier-Bemard et Turenne,
technical specialists
and defence contractors near Paris.

THEORY OF OPERATION

The Somatoscope mixes light from two orthogonal light sources—a

mercury lamp and a halogen
lamp. The light from both sources
enters a glass tube at 90° from each other. As the light waves
beat
against each other, a strong carrier wave of light emerges
and travels down the light tube. (It should
be noted that two
electromagnetic fields superimposed upon each at 90° is a
classic scalar
formation!) As the light travels down the tube,
it passes through a monochromatic filter which
forms it into a
mono­chromatic ray. The ray is then passed through a large coil
that sur­rounds the
tube. The coil's magnetic field divides the
ray into numerous parallel rays that are then passed
through a
Kerr cell which increases the frequency of the rays before being
injected onto the
specimen.

FIGURE 1

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Two light sources: the first (1) an

incandescent one with a wavelength of about 3600 angstrom, the
second (2) an ultraviolet
one with a wavelength of about 2200
angstrom beat against each other to produce a third wavelength
of which passes
through a monochromatic filter (3) to produce
a monochromatic ray. This ray is exposed to magnetic fields
(4)-the Zeeman
effect- that divides tt to produce
numerous parallel rays (5) that. In turn pass through a Kerr-cell
(6) that increases the
frequency. It is this light source,
invisible to the naked eye, that strikes the specimen slides.
The Image is reconstituted by
the microscope. Credit: Guide
Resources

The light, which contains the carrier and a mixture of selected

signals in the UV range, stimulates
the biological material in
the Somatoscope to the point that the specimens give off their
own light.
(Rife referred to this as luminescence.) This is the
key to the ultra-high resolution that has been
achieved by
Gaston Naessens.

Conventional microscopes pass light through the specimen which

theoretically limits the resolution
of optical microscopes to
the wavelength of light. The finest optical microscopes have
achieved
magnification levels of 2,500 diameters. At levels
above this, the resolution is limited by the
wavelength of light
and further magnification merely creates a blur! Higher
resolutions have been
achieved by microscopes which do not use
lenses, but rather apertures which are smaller than the
wavelength of light. One such microscope engineered in Cornell
University has achieved a
resolution of 400 angstroms—a far cry
from the 150 angstroms achieved by Naessens'
Somatoscope.

The Somatoscope does not attempt to illuminate the specimen by

passing light through two small
objects. Instead, the
illumination source is actually stimulating the specimen to the
point it generates
its own light. The light itself expands as it
moves outward and because the specimen itself is
generating the
light, the physi­cal restrictions encountered by regular optical
microscopes do not
apply. By converting the specimen into a
light source, Gaston Naessens has converted the
magnification
problem from one of resolution to that of light detection! At
magnification levels
above 5,000 diameters, light levels drop
off the point that film is necessary, but the resolution is
there.

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To further research along the lines he has pioneered, Gaston

has developed junior models of his
Somatoscope for field use.
These field units allow researchers to obtain illumination and
stimulation
of the specimens of the larger unit. The field units
are capable of magnifying 6,000-7,000 diameters,
although
routine work will usually be at 3,500-4,000 diameters. The lower
light levels of the higher
magnification requires that a lower
level of magnification be accepted for field use in order to
maintain portability in the smaller units. One such unit will be
in use in Colorado Springs at Clifford
and Associates. The
Somatoscope has enabled researchers to discover the importance
of colour and
its relationship to the material being observed.
The wavelengths of light generated are related to the
size of
the object and the health of the cell. For instance, the red
blood cells vary from yellow/green
to orange (540 nm to 580 nm)
and white blood cells are rich in blue/violet (490 nm to 510
nm).
Exposure to toxic materials, even in minute amounts, causes
significant shifts in colour. Even 'safe'
amounts of toxic
materials like mercury and the aluminium in toothpaste cause
significant
degradation to red blood cells as I was able to
witness from specimens on a videotape produced
from the
Somatoscope.
THE SOMATID CYCLE

In a long lost chapter of history in science, a violent

controversy took place in France between the
illustrious Louis
Pasteur and Antoine Bechamp, a noted professor of physics,
toxicology, medical
chemistry, and biochemistry. Bechamp's work
led him to discover 'microzymas' (tiny ferments)
which were
characterised by a host of small bodies in his fermenting
solutions.

After years of study, Bechamp came to the conclusion that these

microzymas were more basic to life
than cells. Even with his
crude equipment, he was able to observe that the microzymas
underwent
dramatic transformations during their life cycle. This
caused Bechamp to champion the idea that the
cause for disease
lay within the body. Pasteur's germ theory held that the cause
came from without
Pasteur's outspokenness helped the germ theory
win out and dominate medical philosophy for the
past century.

Now, a hundred years later, Gaston Naessens has discovered an

ultramicroscopic, subcellular, living
and reproducing
microscopic form which he christened a 'somatid' (tiny body).
This new particle
could be cultured outside the bodies of the
host. Naessens also observed that the particle had a
pleomorphic
(form-changing) life cycle, and had a sixteen-stage life cycle.
Only the first three
stages of the somatid life cycle are
normal. FIGURE 2

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Naessens discovered that when the immune system is weakened or

disrupted, the somatids go
through the other thirteen stages.
The weakening of the immune system could be brought about by a
number of reasons such exposure to chemical pollution, ionising
radiation, electric fields, poor
nutrition, accidents, shock,
depression, and many more.

Incredibly, Naessens' research has resulted in the association

of degenerative diseases (rheumatoid
arthritis, multiple
sclerosis, lupus, cancer and AIDS) with the development of forms
in the sixteen-
stage pathological cycle. The ability to
associate the disease with specific stages has enabled
Naessens
to 'prediagnose' conditions in advance of when they would
clinically appear.

This discovery puts Gaston Naessens at odds with the orthodox

medical philosophy today which has
embraced Pasteur's germ
theory wholeheartedly. Naessens' work is repeatable. The ability
to culture
somatids is a bellwether to the rewriting of
microbiology!

Naessens stated: "I've been able to establish a life cycle of

forms in the blood that add up to no less
than a brand new
understanding of the basis of life. What we're talking about is
an entirely new
biology, one out of which has fortunately sprung
practical applications of benefit to sick people,
even before
all of its many theoretical aspects have been sorted out"
714X

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12/7/2021 Gaston Naessens: Somatids, Somatoscope, & 714X; Alternative cancer treatment; Articles & 2 Patents

The research of Gaston Naessens has culminated in the discovery

of 714X—an enzyme which helps
the immune system to do its job.
714X is a derivative of camphor and is injected
interlymphatically
—a process that the medical fraternity holds
to be impossible. Yet the fact remains that many people
have
learned how to administer the medication through lymph nodes.

When properly administered, 714X stabilises and strengthens the

immune system in most cases.
This allows the immune system to go
about its normal business in ridding the body of disease. In
other words, cancer is treated like an infection, not a state of
cells.

Like Bechamp and Rife before him, Gaston states unequivocally,

"germs are not the cause of, but
the result of, disease".

714X will not help everyone—especially where there has already

been extensive use of
chemotherapy and radiation. (Chemotherapy
and radiotherapy wipes out the immune system and
other bodily
resources.)

THE SECOND CHANCE

The cancer death toll between 1970 and 1986 was approximately 6
MILLION. Sadly, the
conventional treatments of chemotherapy and
radiation therapy are nothing more than slow death
sentences
that enrich the cancer industry. Possible miracle cures are
quickly quashed by the FDA
(Food & Drug Administration) and
the various medical societies around the world. It is a sad
commentary that in a country that prides itself on freedom,
terminally ill patients cannot make an
informed decision to
participate in experimental treatments that may save their
lives.

714X is available in the United States. WRITERS & RESEARCH

is one organisation working
closely with the FDA and the IRB
(Institution Review Board) to do work with 714X legally and
ethically. 714X is an injected medication and must beprescribed
by a doctor.

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