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» LymeNet Flash » Questions and Discussion » Medical Questions » Message from Dr. K. re Amalgams and Microcurrent, Rife, EM Devices

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Author Topic: Message from Dr. K. re Amalgams and Microcurrent, Rife, EM Devices
GiGi
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Sailboat (I can't find the post right now) asked the other day about using microcurrent while still having amalgam fillings in the mouth. I answered her then -- basically, don't do that.

In talking to Dr. Klinghardt about that, he answered per the attached:

"Regarding amalgam fillings and the use of microcurrent:

It is almost ironical if someone has a diagnosis of Lyme disease and has not included the biologically correct removal of the amalgam fillings as an early part of their treatment.

Neurotoxins are cumulative and mercury is a more powerful neurotoxin than the ones created and released by Borrelia and co-infections.

The treatment of the microbes should follow the removal of any neurotoxic foci in the body, starting with the amalgam fillings and root fillings.

My advice rearding the use of microcurrent is dependent on the intelligent or at least common- sense-use of other therapeutic modalities in the proper order when Lyme disease is to be treated successfully. It is in my opinion not possible to treat Lyme without the removal of amalgam fillings first.

What I need to say here very strongly: many Lyme patients are using electromagnetic devices such as Rife instruments, the Doug coil and others - which are all mobilizing mercury from existing amalgam fillings. This fact leads to many catastrophic reactions which are often falsely written off as "die-off effect" or Herxheimer reaction. The same precautions apply here as the ones written for the KMT technology which deals with these problems openly and responsibly

However, if someone chooses to use microcurrent (or other EM-devices) in the presence of amalgam fillings which are constantly outgasing mercury into the brain, there are 3 options:

a) use the microcurrent while chewing on 3-5 tablets chlorella (keep the sludge in the mouth as long as treatment lasts, then spit out and rinse mouth). This will bind and eliminate (via the intestinal tract) all dental toxins mobilized by the flooding of the oral cavity with microcurrent

b) use the electrodes away from the face (i.e. hands and feet)

c) use the biofield treatment modality: 2 signal enhancers (form BioPure) are pulsed with the microbial inhibition frequencies, about 2-3 feet away from the client`s body`. This has a strong photo-optic non-electronic effect on raising specific aspects of the immune system without mobilizing mercury

Dietrich Klinghardt, MD"

Hope that answers all questions clearly.

Take care.

[ 15. June 2006, 02:02 AM: Message edited by: GiGi ]

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humanbeing
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Are there special dentists who help us lymies with amalgam removal? Mine told me there are no studies to show amalgams are linked to chronic disease, they are perfectly safe....(and I am perfectly healthy too)!

--------------------
We are spiritual beings on a human journey...

www.ruggierogallery.com

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SForsgren
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Excellent Excellent information. Something I suspect most people don't recognize but certainly can be very important. Thanks GiGi!

--------------------
Be well,
Scott

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GiGi
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Humanbeing, here is a partial list of published info involving mercury and chronic disease, etc. You might take it to your dentist. Most dentists are exposed to mercury. I know many that are getting treatment - some of them unable to work any longer. Close to 25% of Canadian dentists are on Disability. Health Canada did the survey.

The full article you can find on my doctor's website www.neuraltherapy.com/articles

There are a number of dentists that do the work well. You just have to look around - they do not advertise - just as LLMD's don't! for obvious reasons.

Good luck to you.

Here is the list for your dentist -- do print it for him:

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3 De Boever, E.H., De Uzeda, M., and Loesche, W.J.: Relationship between volatile sulfur compounds, BANA-hydrolyzing bacteria and gingival health in patients with and without complaints of moral malodour. J. Clin. Dent., 4: 114-119, 1994

4 Duhr, E.F., Pendergrass, J.C., Slevin, J.T., and Haley, B.E.: HgEDTA complex inhibits GTP interactions with the E-site of the brain �-tubulin. Toxicol. Appl. Pharmacol., 122: 273-280, 1993

5 Giuliana, G., Ammatuna, P., Pizzo, G., Capone, F., and D'Angelo, M.: Occurrence of invading bacteria in radicular dentin of periodontally diseased teeth: microbiological findings. J. Clin. Periodonto., 24: 478-485, 1997

6 Granlundt-Edstedt, M., Johannson, E., Claesson, R., and Carlsson, J.: Effect of anaerobiosis and sulfide on killing of bacteria by polymorphonuclear leukocytes. J. Periodont. Res., 8: 346-353, 1993

7 Hannah, R.S., Hayden, L.J., and Roth, S.H.: Hydrogen sulfide exposure alters the amino acid content in developing rat CNS. Neurosci. Lett., 99: 323-327, 1989

8 Johnson, P.W., Yaegaki, K., and Tonzetich, J.: Effect of volatile thiol compounds on protein metabolism by human gingival fibroblasts. J. Periodont. Res., 27: 553-561, 1992

9 Khatoon, S., Campbell, S.R., Haley, B.E., and Slevin, J.T.: Aberrant guanosine triphosphate-�-tubulin interaction in Alzheimer's disease. Ann. Neurol., 26: 210-215, 1989

10 Kilburn, K.H., and Warshaw, R.H.: Hydrogen sulfide and reduced-sulphur gases adversely affect neurophysiological functions. Toxicol. Ind. Health, 11: 185-197, 1995

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13 Loomer, P.M., Sigusch, B., Sukhu, B., Ellen, R.P. and Tenenbaum, H.C.: Direct effects of metabolic products and sonicated extracts of Porphyromonas gingivalis 2561 on osteogenesis in vitro. Infect. Immun., 62: 1289-1297, 1994

14 Nair, P.N:R., Sjogren, U., Krey, G., Kahnberg, K.-E., Sundqvist, G.: Intraradicular bacteria and fungi in root-filled, asymptomatic human teeth with therapy-resistant periapical lesions: a long-term light and electron microscopic follow-up study. J. Endodon., 16: 580-588, 1990

15 Pendergrass, J.C., Haley, B.E., Vimy, M.J., Winfield, S.A., and Lorscheider, F.L.: Mercury vapor inhalation inhibits binding of GTP to tubulin in rat brain: similarity to a molecular lesion in Alzheimer diseased brain. Neurotoxicology, 18: 315-324, 1996

16 Pendergrass, J.C., Haley, B.E.: Inhibition of brain tubulin-guanosine 5'-triphosphate interactions by mercury: Similarity to Observations in Alzheimer's diseased brain. Metal ions in biological systems: mercury and its effects on environment and biology (Sigel, H. and Sigel, A., eds) Marcel Dekker, Inc., New York, pp461-478, 1996

17 Pendergrass, J.C., Haley, B.E.: Mercury-EDTA complex specifically blocks brain �-tubulin interactions: similarity to observations in Alzheimer's disease. Status quo and perspectives of amalgam and other dental materials (Friberg L.T. and Schrauzer G.N., eds) Georg Thieme Verlag, Stuttgart, pp98-105, 1995

18 Persson, S.: Hydrogen sulfide and methyl mercaptan in periodontal pockets. Oral Microbiol. Immunol., 7: 378-379, 1992

19 Persson, S., Claesson, R., Carlsson, J.: Chemotaxis and degranulation of polymorphonuclear leukocytes in the presence of sulfide. Oral Microbiol. Immunol., 8: 46-49, 1993

20 Ratcliff, P.: Local predisposing events leading to gingivitis and periodontitis. J. Periodont., 66: 749-750, 1995

21 Reiffenstein, R.J., Hulbert, W.C., and Roth, S.H.: Toxicology of hydrogen sulfide. Annu. Rev. Pharmacol. Toxicol. 109-134, 1992

22 Roth, S.H., Skrajny, B., and Reiffenstein, R.J.: Alterations of the morphology and neurochemistry of the developing mammalian nervous system by hydrogen sulfide. Clin. Exptl. Pharmacol. Physiol., 22: 379-380, 1995

23 Skrajny, B., Reiffenstein, R.J. Sainsbury, R.S., and Roth, S.H.: Effects of repeated exposures of hydrogen sulphide on rat hippocampal EEG. Toxicol. Lett., 84: 43-53, 1996

24 Warenycia, M.W., Goodwin, L.R., Benishin, C.G., Reiffenstein, R.J., et al.: Acute hydrogen sulfide poisoning. Biochem. Pharmacol., 38: 973-981, 1989

25 Safavi, K.E., Rossomando, E.F.: Tumor necrosis factor identified in periapical tissue exudates of teeth with apical periodontitis. J. of Endodontitis, 17(1): 12ff, 1990

26 Maiorino, R.M., et al.:Sodium 2,3-dimercaptopropane-1-sulfonate challenge test for mercury in humans. III. Urinary mercury after exposure to mercurous chloride. J. Pharmacol. Exp. Ther., 277(2): 938-44, 1996

27 Keith, R.L., et al.: Utilization of renal slices to evaluate the efficacy of chelating agents for removing mercury from the kidney. Toxicology, 116(1-3): 67-75, 1997

28 Aposhian, M.M., et al.: Sodium 2,3-dimercapto-1-propanesulfonate (DMPS) treatment does not redistribute lead or mercuri to the brain of rat. Toxicology, 109(1): 49-55, 1996

29 Aposhian, H.V., et al.: Urinary mercury after administration of 2,3-dimercaptopropane-1-sulfonic acid: correlation with dental amalgam score. FASEB J., 6(7): 2472-6, 1992

30 Aposhian, H.V., et al.: Human studies with the chelating agents, DMPS and DMSA. J. Toxicol. Clin. Toxicol., 30(4): 505-28, 1992

31 Hermann, M., Schweinsberg, F.: Biomonitoring for the evaluation of a mercury burden from amalgam fillings. Mercury determination in urine before and after oral doses of 2,3-dimercapto-1-propanesulfonic acid (DMPS) and in hair. Abteilung Allgemeine Hygiene und Umwelthygiene, Universit�t T�bingen, Zentralbl-Hyg-Umweltmed., 194(3): 271-91, 1993

32 Zander, D., et al.: The mercury exposure of the population. III. Mercury mobilisation by DMPS (Dimaval) in subjects with and without amalgam fillings. Medizinisches Institut f�r Umwelthygiene, Heinrich Heine-Universit�t D�sseldorf

33 Molin, M., et al.; Mobilized mercury in subjects with varying exposure to elemental mercury vapour. Int. Arch. Occup. Environ. Health, 63(3): 187-92, 1991

34 Maiorino, R.M., et al.: Determination and metabolism of dithiol chelating agents. XII Metabolism and pharmakinetics of sodium 2,3-dimercapto-1-sulfonate in humans. J. Pharmacol. Exp. Ther., 259(2): 808-14, 1991

35 Gerhard, I., et al.: Diagnosis of heavy metal loading by the oral DMPS and chewing gum tests. Clin. Lab., 38: 404-11,

36 Gonzales-Ramirez, D., et al.: Urinary mercury, porphyrins and neurobehavioral changes in dental workers in Monterrey, Mexico. J. Pharmacol. Exp. Therap., 272: 264-274, 1995

37 Godfrey, M. and Campbell N.: Confirmation of mercury retention and toxicity using (DMPS). J. Advance Med., 7(1): 19-30, 1994

38 WHO Criteria 118, 1991

39 Konetzka, W.: Microbiology of metal transformation, microorganisms and minerals, 317-342, 1977

40 Lexmond, T.-M., et al.: On the methylation of inorganic mercury and the decomposition of organo-mercury compounds - A review. Neth. J. Aci., 24: 79-97, 1976

41 Compeau, G. and Bartha, R.: Methylation and demethylation of mercury under controlled redox, pH and salinity conditions. Appl. & Environ. Microbio. Vol. 48, No. 6, 1203-1207, 1984

42 Edwards, T.: Biosyntheses and degradation of methyl mercury in human faeces. Nature, Vol. 253, 462-464, 1975

43 Blum, J. and Bartha, R.: Effect of salinity on Methylation of mercury. Bulletin Environ. Contam. Toxicol., 25: 404-408, 1980

44 Bertilson, L. and Neujahr, H.Y.: Methylation of mercury compounds by methylcobalamin. Biochemistry, Vol. 10, No. 14, 2805-2828, 1971

45 Imura, N., et al.: Chemical Methylation of inorganic mercury with methylcobalamin, a vitamin B-12 analog. Science, Vol. 172, 1248-1249, 1971

46 Jernelov, A. and Martin, A.: Ecological implications of methal metabolism by microorganisms. Annual Review of Microbiology, 61-77, 1975

47 Lander, L.: Biochemical model for the biological Methylation of mercury suggested from Methylation studies in vivo with Neurospora crassa. Nature, Vol. 230, 452-454, 1971

48 Wataha et al.: Dental Materials. 10(5): pp2988-303, 1994

49 Hamdy, M.K., and Noyes, O.R.: Formation of methyl mercury by bacteria. Appl. Microbiol., Vol. 30, No. 3, 424-432, 1975

50 Brunker, R.L. and Bott, T.L.: Reduction of mercury to the elemental state by a yeast. Appl. Microbiol., Vol 27, No. 5, 870-73, 1974

51 Holm, H.W. and Cox, M.F.: Transformation of elemental mercury by bacteria. Appl. Microbiol., Vol. 29, No. 4, 491&494, 1975

52 Pan Hou, H.S. and Imura, N.: Involvement of mercury Methylation in Microbial mercury detoxification. Arch. Microbiol., 131: 176-177, 1982

53 Bisogni, J.J. and Lawrence, A.W.: Kinetics of mercury Methylation in aerobic and anaerobic aquatic environments. J. Water Pollut. Control Fed., 47: 135-152, 1975

54 Report on the international committee on MAC values on mercury (1969)

55 USEPA document on mercury 1973 & 1984

56 US NIOSH document on mercury 1973

57 Wieliczka, D.M. et al.: Equilibrium vapor pressure of mercury from dental amalgam in vitro. Dent. Mater., 12(3): 179-184, 1996

58 Bjorkman, L. and Lind, B.: Factors influencing mercury evaporation from dental amalgam fillings. Scand. J. Dent. Res., 100(6) 354-60, 1992

59 Lussi, A.: Mercury release from amalgam into saliva: An in-vitro study. Schweiz. Monatsschr. Zahnmed. 103(6): 722-6, 1993

60 Olson, S. and Bergman, M.: Daily dose calculations from measurements of intra-oral mercury vapor. J. Dent. Res., 71(2): 414--23, 1992

61 Vimy, M.J. and Lorscheider, F.L.: Dental amalgam mercury daily dose estimated from intra-oral vapor measurements: A predictor of mercury accumulation in human tissues. The Journal of trace elements in exderimental medicine, 3(1): 11-123, 1990

62 Emler and Cardone: An assessment of mercury in mouth air. Oral Roberts University, March 1985

63 Vimy, M.J. and Lorscheider, F.L.: Serial measurements of intra-oral air mercury: estimation of daily dose from dental amalgam. J. Dent. Res.,64(8): 1072-5, 1985

64 Abraham, J. et al.: The effect of dental amalgam restorations on blood mercury levels. J. Dent. Res., 63(1): 71 & 73, 1984

65 Ott, K. et al.: Mercury burden due to amalgam fillings. Dtsch. Zahn�rztl. Zeitung, 39(9): 199-205, 1984

66 Svare, C.W. et al.: The effects of dental amalgam on mercury levels in expired air. J. Dent. Res.,60(9): 1668-1671, 1981

67 Stortebecker, P.: Mercury poisoning from dental amalgam

68 Schubert, J.: Combined effects in toxicology - A rapid systematic testing procedure cadmium, mercury and lead. J. Toxic. Envir. Health, 4: 763-776, 1978

69 Fedin, B.: Swed. Dent. J. 3: 8-15, 1988

70 Pendergrass, et al.: Neurotoxicology. 18(2): 315-324, 1997

71 Hanson, M.: J. Orthomol. Psychatry, Vol 12, No. 3, 1983

72 Vimy, M.J. and Lorscheider, F.L.J.: Dent. Res., 64: 1069-71, 1985

73 Berglund, A. et al.: Determination of the rate of release of intra-oral mercury vapor from amalgam. J. Dent. Res., 67: 1235-242, 1988

74 Grandjean, P. et al.: Cognitive deficit in 7-year-old children with prenatal exposure to methylmercury. Neurotoxicol. Teratol., 19(6): 417-28, 1997

75 Marlowe et al.: Low mercury levels and childhood intelligence. J. of orthomol. Medicine, Vol 1, No. 1, 1986

76 Reinhardt, J.W.: Side-effects: mercury contribution to body burden from dental amalgam. Adv. Dent. Res. 6:110-3, 1992

77 Vanherle, G.: Dental care using silver amalgam. Verh. K. Acad. Belg., 58(5): 587-634, 1996

78 Danscher, G. et al.: Traces of mercury in organs from primates with amalgam fillings. Department of Neurobiol. Univers. Of Aarhus, Denmark, Exp-Mol-Pathol., 52(3):219-9, 1990

79 Weiner, J.A. et al.: Does mercury from amalgam restorations constitute a health hazard? AU: AD: National Board of occupat. Safety and Health, Solna, Sweden, Sci-Total-Environ. 99(1-2): 1-22, 1990

80 Drasch, G. et al.: Eur. J. Pediatr., 153(8): 607-10, 1994

81 Arvidson, B.: Inorganic mercury is transported from muscular nerve terminals to spinal and brainstem motoneurons. Muscle Nerve, 15(10): 1089-1094, 1992

82 Retrograde axonal transport of mercury in primary sensory neurons innervating the tooth pulp in the rat. Neurosci. Lett. 115(1): 29-32, 1990

83 Aschner: Effects of systemic methyl mercury-adulerated water consumption on fast axonal transport in the rat visual system. Acta Pharmacol. Toxicol. (Copenh.), 59(5): 349-55, 1986

84 Lorscheider, F.L. et al.: FASEB J. 9(4): A-3845. FASEB Annual Meeting, Atlanta, Georgia, 10th March 1995

85 Szucs, A. et al.: Effects of inorganic mercury and methymercury on the ionic currents of cultured rat hippocampal neurons. Cell. Mol. Neurobiol., 17(3): 273-88, 1997

86 Goering et al.: Fundam. Appl. Toxicol., 19: 319-329, 1992

87 Pendergrass, J.C. et al.: Mercury Vapor inhalation inhibits binding of GTP to tubulin in rat brain: Similarity to a molecular lesion in Alzheimer diseased brain. Neurotoxicology, in press, 1997

88 Haley, B.E. et al.: FASEB J. 9(4): A-3845. FASEB Annual Meeting, Atlanta, Georgia, 10th March 1995

89 Duhr, E. et al.: Federations of American Societies for experimental biology (FASEB). 75th Annual Meeting, Atlanta, Georgia. 21.-25 April 1991. Abstract 493. Hg2+ induces GTP-tubulin interactions in rat brain similar to those observed in Alzheimer's disease.

90 Pamphlett, R. and Waley, P.: Motor neurons uptake of low dose inorganic mercury. J. Neurol. Sci., 135(1): 63-7, 1996

91 Oskarsson, A., et al.: Total and inorganic mercury in breast milk in relation to fish consumption and amalgam in lactating women. Arch. Environ. Health, 51(3): 234-41, 1996

92 Amin.Zaki, L., et al.: Methyl mercury poisoning in the Iraqi suckling infant: A longitudinal study over five years. J. Appl. Toxicol., 1(4): 2104, 1981

93 Redhe, O.: Pleva recovery from amyotrophic lateral sclerosis and from allergy after removal of dental amalgam fillings. J. Int. J. Risk Safety Medicine, 4: 229-236, 1994

94 Enwonwu, C.O.: Potential health hazard of the use of mercury in dentistry: Critical review of the literature. Environ. Res., 42: 257-274, 1987

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96 Rosenmann, K.D., et al.: Sensitive indicators of inorganic mercury toxicity. Arch. Environ. Health, 41: 208-215, 1986

97 Desi, I., et al.: Effect of subchronic mercury exposure on electrocorticogram of rats. Neurotoxicology. 17(3-4): 719, 23, 1996

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109 Drasch et al.: Trace elements in medicine and biology. 9(2):82-7, 1995#

110 Hahn, L.J., et al.: FASEB J., 4(14): 3256-60, 1990

111 Vimy, M.J., et al.: Am. J. Physiol., 258(Pt. 2): R939-45, 1990

112 Vimy et al.: Mercury from maternal ``silver'' tooth fillings in sheep and human breast milk. Biological Trace Element Research, V56, pp143, 1997

113 Wenstrup, D., et al.: Trace element imbalances in isolated subcellular fractions of Alzheimer's disease brains. Department of Chemistry, University of Kentucky, Lexington. Brain Res., 533:1, 125-31, 1990

114 Nylander, M., et al.: Mercury concentrations in the human brain and kidneys in relation to exposure from dental amalgam fillings. Swe. Dent. J., 11:5, 179-87, 1987

115 Friberg, L. et al.: Kvicksilver I centrala nervsystemet I relation till amalgamfyllningar (Mercury in the central nervous system in relation to dental amalgam). Lakartidningen, 83:519-22, 1986

116 Eggelston, D.W., et al.: Correlation of dental amalgam with mercury in brain tissue. J. Pros. Dent., 58: 704-7, 1987

117 Schiele et al. in 1984

118 Nylander, M., et al.: Mercury concentration in the human brain and kidneys in relation to exposure from dental amalgam fillings. Swed. Dent. J., 11(5): 179-87, 1987

119 Weiner, J.A. and Nylander, M.: The relationship between mercury concentration in human organs and different predictor variables. National Board of Occup. Safety and health, Solna, Sweden. Sci-Total-Environ., 138(1-3): 101-15, 1993

120 Drasch, G., et al.: Silver concentrations in human tissues, their dependence on dental amalgam and other factors. Trace Elements in Medicine and Biology, 9(2): 82-7, 1995

121 Smith, D.H.: Science, 156, 1114, 1967

122 Duhr, E. et al.: Hg2+ induces GTP-tubulin interactions in rat brain similar to those observed in Alzheimer's disease. FASEB, 75th Annual Meeting, Atlanta, Georgia, 21.25 April 1991, Abstract 493

123 Pendergrass, J. et al.: The deleterious effects of low micromolar mercury on important brain and cerebrospinal fluid protein. American Association of pharmaceutical scientists, Annual Meeting, 5-9 November, 1995, Miami

124 Pendergrass, J.C. et al.: Mercury vapor inhalation inhibits binding of tubulin in rat brain: Similarity to a molecular lesion in Alzheimer disease d brain. Neurotoxicology, In Press June-July 1997

125 Lorscheider, F.L., et al.: Toxicity of ionic mercury and elemental mercury vapour on brain neuronal protein metabolism. 1994

126 Summers, A.O. et al.: Mercury released from dental ``silver'' fillings provokes an increase in mercury- and antibiotic-resistant bacteria in oral and intestinal floras of primates. Antimicrob. Agents Chemother. 37(4): 825-34, 1993

127 Edlund, C. et al.: Resistance of the normal human microflora. Mercury and antimicrobials after exposure to mercury from dental amalgam fillings. Clin. Inf. Dis. 22(6): 944-950, June 1996

128 Liebert, C.A. et al.: The impact of mercury released from dental ``silver'' fillings on antibiotic resistances in the primate oral and intestinal bacterial flora. Met. Ions. Biol. Syst., 34:441-60, 1997

129 Catsakis, L.H., Sulica, V.I.: Allergy to silver amalgams. Oral Surg. Oral Med. Oral Pathol., 46(3): 371-5, 1978

130 Stejskal, V.D.M., et al.: The lymphocyte transformation test for diagnosis of drug-induced occupational allergy., Journal of Allergy and Clinical Immunology 77, 411-426

131 Stejskal, V.D.M. et al.: Lymphocyte transformation test for diagnosis of isohia-zolinone allergy in man., J. of Investigative Derma-tology 94, 798-902

132 Stejskal, V.D.M. et al.: Allergy to drugs and other chemicals diagnosed by the presence of specific memory cells in human blood. In realm of tolerance. Edited by P. Ivanyi. Pp. 213-224. Springer-Verlag, Berlin

133 Wilhelm-M, Dunninger, P. et al.: Effects of amalgam on cells of the immune system. Einfluss von Amalgam auf Zellen des Immunsystems. Med. Poliklinik der Universit�t W�rzburg, Dtsch. Zahn�rztl. Z., 46(8): 544-7, 1991

134 Adverse immunological effects and autoimmunity induced by dental amalgam and alloy in mice. Hultmann: FASEB J, 8(14): 1183-90, 1994

135 Hultman: Murine mercury-induced immune-complex disease: effect of cyclophosphamide treatment and importance of T-cells., Br. J. Exp. Pathol., 70(3): 227-36, 1989

136 Hultman: Murine susceptibility to mercury. II. Autoantibody profiles and renal immune deposits in hybrid backcross and H-2d congenic mice. Clin. Immunol. Immunolpathol. 68(1): 9-20, 1993

137 Enestrom, S., Hultman, P.: Does amalgam affect the immune system? A controversial issue.; Int. Arch. Allergy Immunol., 106(3): 180-203, 1995

138 Warfvinge, G., Larsson, A.: Contact stomatitis to mercury associated with spontaneous mononuclear cell infiltrates in brown Norway (BN) rats with HgCl2-induced autoimmunity. J. Oral Pathol. Med. 23(10): 441-5, 1994

139 Kosuda, L.L.; et al.: Mercury-induced renal autoimmunity in BNLEW. 1N chimeric rats., Cell. Immunol. 155(1): 77-94, 1994

140 Sato, K., et al.: An Epidemiological study of mercury sensitization. Allergology International, 46:201-6, 1997

141 Summers, A.O., Sugarman, L.I.; J. Bacteriol. 119, 242, 1974

142 Katsunuma Exercise-induced anaphylaxis: improvement after removal of amalgam in dental caries., Ann. Allergy, 64(5): 472-5, 1990

143 Caron, G.A., et al.: Lympho-cyte transformation induced by inorganic and organic mercury., International Archives of Allergy 37, 76 87

144 Bolewska, J., et al.: Oral mucosal lesions related to silver amalgam restorations., Department of Oral Medicine and Oral Surgery, University Hospital, Copenhagen, DK, Oral-Surg. Oral-Med.Oral-Pathol., 70(1): 55-8, 1990

145 Finne, K. et al.: Oral lichen planus and contact allergy to mercury. International Journal of Oral Surgery 11, 236-239

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Clancy
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GiGi,

This post got me wondering if detoxing with amalgams applied to Rechts-Regulat, foot pads, etc. as well as micro current. I think that I read here that Dr.K applies it to infra red saunas, also. Thanks for all your great posts.

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SForsgren
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I think it is unlikely that foot pads would be problematic. They are not mobilizing metals to my knowledge. They remove toxins. With the other devices discussed here, they mobilize metals. Will be interested in other people's thoughts, but I don't see foot pads as having a risk of metal mobilization.

--------------------
Be well,
Scott

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GiGi
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Rechtsregulat is really a regulator of all body systems - all the 1000 enzymes contained in it affect every function our body needs to perform and is often not able to perform because of a misguided immune system. Increasing metabolism, correcting pH, cleansing of the blood, loss of vitality, sleep problems, toxic tissue. All is written up in the booklet. My advice - take it.

Dr. K. told here what he thinks of amalgams in a sick body and the use of KMT.

FIR sauna are very, very effective. However: peer reviewed literature shows that sweatting during sauna therapy elimintes high levels of toxic metals, organic compounds, dioxin, and other toxins. Sauna is ideal to mobilize toxins from its hiding places. However, during a sauna, toxic metals can als be displaced from one body compartment into another. This means mercury can be shifted from the connective tissue into the brain.

You can protect yourself somewhat with chlorella, cilantro and garlic. But he does not recommend doing Sauna in the early stages of detoxing. But rather when the bulk has been removed, and then toward the latter half of the detoxing the danger is not that great.

He does not suggest using a sauna when someone still has a mouthful of amalgams. We had our sauna very early on into my disease, but he did not recommend using it until I had detoxed metals for quite a while. I think it was almost two years for me before I got into it.

It is recommended that you constantly soak up the sweat with towels, disposing them in a bag outside the sauna. Mercury as you detox it turns into vapor, odorless, invisible, and clings to the walls! Wiping it off from your body prevents reabsorption through the skin. That stuff is b a d !!! And I am not an admirer of the dentists that tell us it's innocent.

Footpads -- I made a note of some of the side effects Dr. K. recited somewhere sometime: "The only side effect I have observed so far is the occasional irritation of the skin. In this case the pad cannot be applied with the tape provided and a switch to a non-allergic medical tape.

I have also seen the eruption of chronic underlying fungal infections at the sole of the foot. I have published a paper on the relationship between heavy metals and fungi:

Fungi store metals in their cell wall and help the body to keep the toxin in a biologically contained form. As we remove the metals from the fungi with the footpad, the immune system starts to attach the fungi int he skin and there will be inflammation, skin eruptions and discomfort. In this case I use a medical antifungal cream, evaluate the client's diet and change it. After the situation is resolved it is safe to return to the use of the pad."

Amalgams are bad news - whichever way you turn or twist it.

Take care.

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