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Bruce Phillip Kyle, M.D.Stavtrupvej
7ADK-8260 Viby JTlf: (+45) 86-289688Fax:
(+45) 86-289644E-mail: bpkyle@inet.uni-c.dk |
Danish Medical Association (DADL)
General Practitioners Association (PLO)
International Academy of Oral Medicine &
Toxicology (IAOMT)
American College for Advancement in Medicine
(ACAM)
American Board of Chelation Therapy (ABCT)
Scandinavian Board of Chelation Therapy (SBCT)
Danish Association of Orthomolecular
Medicine (DSOM) |
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As a medical doctor who has been working
with amalgam toxicity for seven years in a
clinical setting, I wish to comment the EU
preliminary draft on dental amalgam. My
remarks are to be seen in context with the
excellent commentaries by Dagfinn Reiersøl,
Henrik Lichtenburg and Poul Møller, which
reflect the seriousness with which this
issue is considered by growing numbers of
people in the United States, Canada and
Europe, who are not prepared to accept
“business as usual” from closed-door panels
of experts, who dismiss the growing body of
information on the dangers of amalgam
fillings in such biased fashion as evidenced
by the draft report.
My clinic in Aarhus Denmark has functioned
as a kind of “place of last resort” for
Scandinavian patients, who have health
problems, which they suspect have arisen
because of mercury toxicity. Typically,
these persons have sought help in the
established hospital system before finding
their way to my medical practice. Many have
spent considerable sums of money with
alternative therapies such as acupuncture or
zone therapy, which oftentimes give
temporary relief of symptoms, but which in
the long run do not solve the major problem,
in so far as that problem turns out to be
mercury toxicity.
The health risks associated with dental
amalgam are part of the larger problem
environmental illness. Sensitivity to heavy
metals, chemicals and other toxic factors
from the environment present a new kind of
challenge to the clinician. Chronic toxicity
from environmental factors is often not
accompanied by a typical set of symptoms.
Diagnosis is therefore one of the more
difficult challenges in medical practice.
Unless a doctor has taken a special interest
in this area, it is unlikely that he will
have it on his list of possibilities, when
the patient consults him for help.
Chronic mercury toxicity exemplifies this.
Because the patient will often present with
mental, emotional and/or neurological
complaints, there is the tendency to see
them as psychogenic, especially when lab
results fail to turn up anything. Their
symptoms are considered as either
psychiatric in origin or the effects of
psycho-social stress. In both situations the
real problem goes untreated. In section
5.3.8.2 of the draft report the working
group makes this mistake. They cite scores
of studies which argue for a psychogenic
component as the cause for why some persons
complain that dental amalgams are making
them sick. The working group seems to have
forgotten that symptoms of mental-emotional
agitation are cardinal signs of mercury’s
neurotoxicity.
This tendency of orthodox dentistry to
dismiss the symptoms of the mercury toxic
person as psychosomatic goes hand in hand
with blood- and urine-mercury determinations
to disprove the diagnosis. The draft report
is true to form in this respect and totally
out of step with medical toxicology. Its
conclusion that “…no systemic toxic effects
have been shown to be related to the release
of mercury from dental amalgam fillings” is
based upon numerous scientific articles,
that are unaware of the well documented fact
among researchers, who have studied the
subject, that mercury levels in the blood
and urine are not reliable measures of toxic
effect for low level chronic mercury
exposures. As Dagfinn Reiersøl has pointed
out in his commentary, even their own expert
references (1991 WHO report, p. 61; 1993
USPHS report, p.III-4) point this out.
Indeed, their is evidence that persons who
suffer mercury poisoning show “retention
toxicity”, - that is, urine mercury levels
that are exceedingly low despite high tissue
levels of mercury. Therefore, the tendency
of the working group to disqualify vast
amounts of patient data showing possible
systemic toxic effects from dental amalgam
on the basis of blood and urine mercury
levels is not only unacceptable, but also
raises questions as to their knowledge level
and/or motives.
There is a growing body of international
experts who argue that a mobilisation test
is required in order to evaluate the mercury
toxic patient. It has been shown that the
level of mercury exposure is best quantified
by analysis of urine both before and after
administration of the compound
2,3-dimercapto-propan-1-sulfonat (DMPS).
Without such a metal-binding (chelating)
agent the accumulated deposits of mercury in
the various tissues will not show themselves
in urine or blood . In my own practice we
have used the DMPS-mobilisation test (a.m.
Daunderer) as the gold standard for
evaluating patients who suspect their
symptoms arise from dental amalgams.
I would like to conclude this short
commentary with a question. In this day and
age of ours when environmental toxicity is
so widely spoken of in the media with
regards the alarming rise in cancer,
especially among young people, who among us
truly believes that they can afford extra
toxicity in the form of mercury from dental
amalgams? It was proven during the 1980’s
that mercury vaporizes from amalgam and
accumulates in the body as an inner
pollutant, especially in the nervous system.
These are commonly accepted facts. In 1997
the amalgam debate hinges solely on the
question of how much is enough to give you
MS, ALS, Alzheimers, Parkinsonism and other
forms of free radical degenerative disease.
Do we want amalgams in the mouths of our
children? No right thinking, rational person
can answer “yes” to that question, when
presented with the scientific evidence that
is available today.
Here we must emphasize that an intuitive
sense for just how poisonous mercury is, is
an important prerequisite for interpreting
the voluminous number of new studies and
data concerning the amalgam problem. Chang
et al (1972 and 1974) showed in animal
studies that less than 1 ppm (part per
million) of mercury damaged the blood-brain
barrier within hours of test exposure,
hereby increasing permeability for other
substances from the plasma that would
normally have been excluded. In other words,
mercury’s effect enhances the damaging
effects of other pollutants by introducing a
toxic synergy on the level of nerve cells,
the medium of thinking and emotion for us as
human beings.
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