Page 17 - Spring2018
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Many symptoms of mercury toxicity are  unpopular topic. Thus, the public may receive   Much
            vague, resembling premature cellular aging.  mixed messages from health authorities and agen-  mercury
            On the other hand, some symptoms are more  cies about the risks of routine mercury exposures,
            distinct, a case in point being erethism. The  depending on whether the exposure involves  exposure is
            term erethism (or reddening), which derives  dentistry, seafood consumption or vaccines.  iatrogenic—
                                          3
            from a person’s tendency to blush,  covers a   For most people, the major sources of mer-  caused by
            constellation of personality traits including ti-  cury exposure (Table 1) are elemental mercury
            midity, diffidence, contentiousness, insecurity,  vapor from dental amalgams and methylmer- health care
            bluntness, rigidity, excitability and hypersensi-  cury (an organic mercury compound) from   providers or
                                                 4-6
            tivity to criticism and to sensory stimulation.   dietary fish. Ethylmercury (another organic   institutions—
            Considering mercury’s subtle but reproducible  mercury compound) in certain thimerosal-
            effects on emotions, it is likely that a number  containing vaccines provides smaller amounts,  making it an
            of problems blamed on character, personality  but these can be highly toxic during the vulner-  unpopular
            or stress may in fact be caused or compounded  able windows of gestation and early childhood.  topic.
            by low-level mercury toxicity.               All three forms of  mercury are easily
                                                      absorbed and readily distributed throughout
            WIDESPREAD EXPOSURE                       the body. Being lipophilic (having an affinity
            AND TOXICITY                              for lipids), they leave the bloodstream quickly,
               Health authorities are unlikely to provide  passing through biological membranes and
            useful guidance on mercury risks, for several  concentrating in cells, including brain cells.
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            reasons. First, mercury is both technically and  Mercury is especially drawn to high-sulfur
            politically difficult to study; thus, scientific  organelles (specialized cell structures) such
            conclusions about some risks remain couched  as mitochondria. Once inside a cell, mercury
            in uncertainty. Second, mercury’s effects are  (chemical symbol Hg) is soon oxidized to Hg2+,
            non-specific and multifactorial. Finally, much  which, as a hydrophilic (water-loving) and li-
            exposure is iatrogenic—caused by health  pophobic form of mercury, cannot easily pass
            care providers or institutions—making it an   through biological membranes. This form of



                                                      ARTICLE SUMMARY
             •  The chronic effects of cumulative, low-dose mercury exposure are under-recognized by both mainstream and alter-
                native health authorities and consequently by the public. Mercury can cause or contribute to most chronic illnesses,
                including neurological disorders, cardiovascular disease, metabolic syndrome, chronic fatigue, fibromyalgia, adrenal
                and thyroid problems, autoimmunity, digestive disorders, allergies, chemical sensitivities, mental illness, sleep disorders
                and chronic infections such as Lyme and Candida. Mercury toxicity should be suspected in individuals experiencing
                multiple health problems.
             •  Diagnosis of chronic mercury toxicity is often difficult because the body’s natural defenses may mask or delay symp-
                toms. Natural defenses are a function of genetic susceptibility, epigenetic factors, micronutrient status and allostatic
                load (cumulative wear and tear on the body). Furthermore, individuals who retain mercury may counterintuitively
                show low levels in blood, urine and hair.
             •  The developmental window from conception through early childhood is one of extreme vulnerability to mercury.
                Mercury is an epigenetic toxicant (affecting future gene expression) as well as a neurotoxicant. Damage may be
                permanent; therefore, prevention is key.
             •  For most people, mercury is the most significant toxicant in the body. By promoting oxidative stress and depleting
                antioxidant defenses including the glutathione system, mercury impairs the body’s response to toxicants in general—
                including to mercury itself.
             •  Mercury toxicity creates a need for extra nutrition, both to repair damage and to provide ample enzyme cofactors,
                which can push blocked enzymes. Carbohydrate intolerance can be a symptom of mercury toxicity, and fat can be
                a preferred fuel. Many people with chronic mercury toxicity have found a nutrient-dense diet to be a useful starting
                point for symptom relief. Individualized supplementation may also be helpful to overcome the extreme nutritional
                depletion and unnatural toxic state.

            SPRING 2018                              Wise Traditions                                                   15
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