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Mercury
Accumulation in Autistic Children: A Possible
Consequence of Stealth Virus Infection
and an Additional Rationale for the Therapeutic
Use of Humic/Fulvic Acids
The
prevailing concept that the body's sole source of
cellular energy is from the metabolism of foods has
been challenged by studies that have identified
energy generating materials in virus infected cells.
These materials were termed alternative cellular
energy pigments. ACE pigments are capable of
donating electrons for metabolic reactions and may
also generate a type of biophysical force that has
yet to be fully understood. ACE pigments generated
in stealth virus cultures contain various types of
minerals. Both in this regard and in several other
shared properties, ACE pigments are comparable to
humates. These materials were previously thought to
be partial breakdown products of ancient plant
materials as they slowly decay towards becoming coal
or oil. More recently humates have been viewed as
re-synthesized organic materia ls that are rich in
aromatic compounds that are bound (coordinated) by
different metals. The metals are thought to
facilitate the passage of electrons and may also
transmit other energies. Humates can both absorb
metals from the environment and deliver metals to
living cells. They can also function in a
buffering-like capacity by reducing the levels of
those metals that are in relatively high
concentrations within an environment, while at the
same time provide those metals for which there is a
deficiency. Humates have been extensively used in
agriculture and are also available as dietary
supplements.
Some
parents of autistic children have attributed their
child's illness to mercury toxicity. Mercury is
included in various vaccines in the form of a
preservative called thimerosal. Mercury poisoning
can cause neurological damage and conceivably
certain children may be uniquely susceptible to its
toxic effects. It is unlikely to be the underlying
cause of autism, however, since neuropeptide changes
are present in cord blood samples of children who
subsequently become autistic. Autistic children show
lower levels of mercury in hair analyses compared to
normal children. This suggests that they may be
accumulating mercury, possibly in the formation of
ACE pigments. Litigation is underway concerning
possible Industry and Government negligence in
disregarding the potential toxicity of thimerosal in
vaccines. It would be ironic if i ndeed the mercury
obtained from the vaccines was actually being used
productively by the body in the formation of ACE
pigments.
The
ingestion of humates and/or the humic and fulvic
acids obtained from humates may help provide a
substitute for, or at least the building blocks for
the formation of ACE pigments. Stealth virus
cultures undergo a repair process attributable to
ACE pigments. An additional benefit of ingesting
humates is the potential capacity to absorb those
minerals that may be in abnormally high
concentrations. Humates have a high absorptive
capacity for mercury and clinical studies
documenting the excretion of mercury in patients
consuming humates as dietary supplements would be of
interest. More important will be a determination of
any clinical changes occurring in the patients.
The
increasing incidence of autism is consistent with an
infectious cause. Stealth-adapted viruses have been
regularly cultured from children with autism and
related diseases. Several stealth viruses were
unequivocally derived from African green monkey
simian cytomegalovirus. Infected monkeys were
routinely used for the production of live polio
virus vaccines. The Food and Drug Administration has
confirmed the presence of simian cytomegalovirus DNA
in some of the licensed lots of polio vaccines
approved for use in the United States . It would be
regrettable if unnecessary focusing on thimerosal in
vaccines were to delay official efforts to search
for infectious agents inadvertently int roduced into
humans through vaccines.
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