B Windham(ED)




Seizures are a result of sudden, brief electrical changes or disturbances in the brain.  Epilepsy is where there are chronic, recurrent seizures. Some seizures are as a result of metabolic or chemical imbalances, alcohol or drug use, cardiac disease, infectious disease, toxic neurological effects, etc.  Syncope involves losing consciousness, but for non-epileptic reasons such as  reduced blood flow to the brain, hypoglycemia, insulin resistance, etc. Epilepsy affects about 2 million people in the U.S., with a higher incidence of seizures. (41)

    The central nervous system has 2 major divisions- central nervous system and peripheral nervous system.  The peripheral nervous system has 2 divisions, somatic and autonomic.  The autonomic nervous system exercises control over automatic and involuntary functions of the body such as heart rate, respiration, etc.  Seizures involve a complex interaction between the autonomic nervous system and the central nervous system.  Seizures are often preceded by a partial seizure or aura having varied characteristics, which can warn those susceptible to seizures of an imminent seizure.  Some can actually control or prevent actual seizures by preventive or biofeedback measures (41).  Anti-epileptic drugs (AEDs) are commonly used to control seizures but sometimes are not effective and sometimes have adverse long-term health effects, including inducement of birth defects/congenital conditions in use by pregnant women or infants.

    Seizure triggers include low blood sugar, dehydration, fatigue, lack of sleep, stress, temperature extremes, depression, flashing lights, allergens, caffeine, alcohol, aspartame, pesticides, toxic metals.  The most common allergen triggers are wheat, milk, and petrochemicals (41). Identification and avoidance of such triggers usually reduces effects.  Caffeine causes release of adrenaline which has blood sugar effects that can trigger seizures. Similar for alcohol, and aspartame an excitotoxin that has trigger effects especially on those subject to depression or mood disorders.  Similar for MSG, another common exicitotoxin (42).  As will be documented exposures to mercury from dental amalgams and toxic metals can also commonly trigger and be factors in seizures and epilepsy, with improvement after amalgam replacement and detoxification.


II. Mercury exposure and chronic health effects

Dental amalgam is the largest source of both inorganic and methyl mercury in most who have mercury amalgam fillings 1.  Those with several amalgam fillings have on average at least 10 times as much mercury exposure as those without amalgam fillings. After replacement of mercury amalgam fillings, the level of mercury in saliva and excretion declines approximately 90%.   Prior to vaccinations, the largest source of mercury exposure of a fetus or infant is from the mother’s dental amalgam 2.  Over the last decade, most vaccinations contained high levels of mercury and were the largest source of mercury exposure in most infants and young children 3.


Amalgam dental fillings produce voltaic electrical currents in the teeth which push high levels of  mercury into the gums and oral mucosa 4, increase mercury vapor release into oral air and saliva 1, where it is distributed throughout the body and causes significant harmful effects.  These currents are measured in micro amps, with some measured at over 4 micro amps. The central nervous system operates on signals in the range of nano-amps, which is 1,000 times less than a micro amp 4.

These voltaic currents and the resulting high levels of mercury exposure are documented to often have significant neurological effects.39 Negatively charged fillings or crowns push electrons and mercury into the oral cavity since saliva is a good electrolyte and cause higher mercury vapor losses.5. Mercury and other metals accumulate in the gums and oral mucosa at the base of teeth with amalgam fillings or metal crowns over amalgam, and is called mercury tattoos 4.  Patients with autoimmune neurological conditions caused by mercury 38,39- like MS,  depression,  epilepsy, etc. are often found to have a lot of high negative current fillings 5.

In addition to its extreme neurotoxicity and immunotoxicity, mercury commonly causes autoimmunity which can also be a factor in conditions like epilepsy, MS, lupus, etc.22, 8,38,39 Prenatal exposure to mercury has been found to predispose animals and infants to seizures and epilepsy. 6, 7,2







A major factor in epilepsy has been found to be essential mineral deficiencies and imbalances- such as magnesium, zinc, calcium,etc.13-18   Mercury is well documented to cause cell membrane permeability changes, mineral efflux from cells, leaky gut, and enzyme blockages that commonly result in essential mineral deficiencies and imbalances 14-20,8. Mercury causes significant destruction of stomach and intestine epithelial cells, resulting in damage to stomach and intestinal lining which along with mercury’s ability to bind to SH hydroxyl radical in cell membranes alters permeability 14-16, 3 and adversely alters bacterial populations in the intestines causing leaky gut syndrome with toxic incompletely digested complexes in the blood 14-20,3,as well as poor nutrient absorption 14-20.

Some of the main mechanisms of toxic effects of metals include cytotoxicity; changes in cellular membrane permeability; inhibition of enzymes, coenzymes, and hormones; and generation of lipid peroxides or free radicals- which result in neurotoxicity, immuno toxicity, impaired cellular respiration, gastrointestinal /metabolic effects, hormonal effects, and immune reactivity or autoimmunity 14-23,2-9,39. Also mercury binds with cell membranes interfering with sodium and potassium enzyme functions, causing excess membrane permeability, especially in terms of the blood-brain barrier.14-16  Less than     1 ppm mercury in the blood stream can impair the blood- brain barrier.

Mercury’s forming strong bonds with and modification of the-SH groups of proteins causes mitochondrial release of calcium 18,14,16,3,40, as well as altering molecular function of amino acids and damaging enzymatic processes 15,16,3,40, resulting in improper cysteine regulation 19,20, inhibited glucose transfer and uptake 15,14, damaged sulfur oxidation processes 19,20,40, reduced glutathione availability 14  (necessary for detoxification), and neurological effects 22,18,38,23. The essential mineral deficiencies and imbalances have been found to be a major factor in Epilepsy, and correcting mineral imbalances has been found to cause significant improvement in epilepsy.13,5,6


A large epidemiological study by the National Institute of Health, the nation's principal health statistics agency,  found a significant correlation between having a larger number of amalgam fillings and people suffering from conditions such as multiple sclerosis and epilepsy 24. Fewer of those with these conditions have zero fillings than those of the general population while more of those with the condition have 17 or more amalgam surfaces than in the general population.   Other studies have found similar connections between vaccinations containing mercury and epilepsy.23,3,25

A doctor with extensive experience in researching and treating mercury toxicity has found that blocked nerve ganglions are  a common cause of seizures, migraines, and other chronic neurological problems.6  Based on his experience Dr. Klinghardt has found that the majority of such conditions are due to dental metals and toxins related to root-canaled teeth or improperly healed tooth extraction sites(cavitations).  He finds that after treatment to unblock the ganglions and mercury detox or cavitation treatment, most patients rapidly recover from such conditions. Numerous other doctors whom he has trained through seminars and courses have had similar experience.


Other doctors treating autism, including seizures which are common in autism, found that mercury and other toxic metals disable the metallothionein function that has several major metabolic and neurological functions. This results in inability to excrete toxic metals, accumulation of mercury and other toxic metals, inability to detoxify mercury and other toxic metals, significant imbalances in zinc/copper levels in the brain and G.I. tract, and major neurological and digestive system effects. 30


Another researcher 28 who has developed test equipment and tested epilepsy/seizure patients has found the following commonly present in epilepsy/seizure patients: Ascaris (pet hookworm) larvae in brain, bacterial infections, viruses, dental metals, vanadium(natural gas leak), and other toxins including PVC, titanium, zirconium, asbestos, lead, solvents, ergot(mold).   She also finds that malvin can provoke seizures: the coloring in grapes, blueberries, strawberries, plums, etc.- and which is also found in chicken and eggs.  After determination of the factors involved for a given patient and treatment she says most patients are cured. The main treatments are recommended for most cases: dental metal and cavitation checks and cleanups, avoidance and detox of environmental toxins,   parasite cleanse and kidney/liver cleanses. Other doctors have likewise found that patients with toxic exposures and weakened immune systems are more susceptible to parasites and biological invaders which must also be treated.29

III.  Alternative Treatments of Epilepsy and Seizures


Most patients with epilepsy recovered or had significant improvement after amalgam replacement 5,6,8-12,26-29    and likewise for many with autism and seizures who were treated for mercury toxicity by treatment clinics.30

        For reasons previously documented and further documented by medical studies and clinical experience in references cited, supplementation alternatives are often beneficial in treatment of seizures and epilepsy.  B vitamins, essential minerals, some herbal products, some amino acids and essential fatty acids are often beneficial. Vitamin B6 plays an important role in the conversion of glutamic acid to GABA (gamma-aminobutyric acid). GABA is the principal inhibitory neurotransmitter in the brain.  Impairment of GABA neurotransmission processes has been found to often be a factor in seizures.  B6 deficiency can result in reduced GABA production. (41) Other B vitamins also are necessary for proper brain function.  B13 also has been found to reduce seizures in some. Vitamin D and Vitamin E have also been found to be beneficial in reducing seizures and seizure severity.  Magnesium deficiency has been shown to increase seizures in some and be a factor in some seizures; manganese aids in sugar metabolism, selenium deficiency can result in deficient glutathione peroxidase which can be a factor in some seizures. Supplementation of these as well as zinc and calcium have been found to reduce seizures in many. (41,etc.)  Diet measures including avoidance of obesity and insulin resistance, along with certain amino acids and essential fatty acids have been found to reduce seizues in many. Taurine is an inhibitory amino acid and like GABA has been found to be effective in reducing seizure activity in some.  Evening primrose oil has been found to reduce seizures in some. Regular exercise has also been found to reduce seizures in most and to improve general well-being. The herbs Black Cohosh, Lobelia, and coleus forshkohlii extract have been found to be beneficial in some (41).  Relaxation techniques such as yoga and biofeedback techniques have been found helpful by some. 


(1) Dental amalgam is the largest source of both inorganic and organic mercury in most who

have amalgam fillings;  DAMS Fact Sheet with peer-reviewed documentation,  www.flcv.com/damspr1.html

(2)  Prenatal and Neonatal Mercury Exposure and Related Health Effects,  B. Windham (Ed),


(3) Mercury from Vaccinations is responsible for a major epidemic of developmental conditions

during the past decade,  Annotated Bibliography, B. Windham(Ed),                                   (over 200 peer-reviewed studies)                www.flcv.com/kidshg.html

(4) "Oral galvanism: the battery in your mouth," B.Windham (Ed.), 2002,                                 (over 100 peer reviewed studies) www.flcv.com/galv.html

(5)   (a)Huggins HA, Levy,TE, Uniformed Consent: the hidden dangers in dental care, 1999,

       Hampton Roads Publishing Company Inc;   & (b) Hal Huggins, Its All in Your Head, 1997;  & (c) Toxic Elements Research Foundation, Colorado Springs Colorado, Survey of 1320 patients being treated for heavy metal toxicity, 2001.  800-331-2303

(6) D.Klinghardt(MD), “Migraines, Seizures, and Mercury Toxicity”, Future  Medicine Publishing, 1997,       & Migraines, Seizures, and Mercury Toxicity;  Klinghardt D.  Alternative Medicine Magazine,             Issue 21 Dec, 1997 / Jan, 1998.    http://www.healingartscenter.com/Library/articles/art10.htm 

(7) Szasz A, Barna B, et al; "Effects of continuous low-dose exposure to organic and inorganic mercury during development on epileptogenicity in rats." Neurotoxicology. 2002 Jul;23(2): 197-206. szente@bio.u-szeged.hu

(8)  MELISA Medical Labs, www.melisa.org &    Stejskal J,  Stejskal V. The role of metals in autoimmune diseases and the link to neuroendocrinology  Neuroendocrinology Letters, 20:345‑358, 1999.  www.melisa.org/knowledge/education14.html

(9) M. Davis, editor, Defense Against Mystery Syndromes, Chek Printing Co., & March, 1994 (case histories documented); www.amalgam.org

(10) The Tribune, Mesa, Az., 13 Apr 1998, (Paul Mills, Apalachee Junction)

(11) Great Plains Laboratory www.greatplainslaboratory.com/test19.html

(12) "Psychiatric Disturbances and Toxic Metals," Townsend Letter for Doctor's & Patients April 2002; & Alternative & Complementary Therapies (a magazine for doctors), Aug 2002.

(13) Ward Dean, "Controlling Seizures: A Nutritional Approach," Sep 2000, www.vrp.com

(14) "Metabolic effects of Mercury Exposure, 2003," B. Windham (Ed.), www.flcv.com/damspr18.html; & Trace elements in hair of epileptic and normal subjects.  Sci Total Environ. 1987 Dec;67(2-3):215-25, Shrestha KP, Oswaldo A.

 (15)  (a)W.Y.Boadi et al, Dept. Of Food Engineering and Biotechnology, T-I Inst of Tech., Haifa, Israel,

            “In vitro effect of             mercury on enzyme activities and its accumulation in the first-trimester human placenta”, Environ Res, 1992, 57(1):96-106;& “In vitro exposure to mercury and cadmium alters term human placental membrane fluidity”, Pharmacol, 1992, 116(1): 17-23;  & (b)J.Urbach et al, Dept. of Obstetrics & Gynecology, Rambam Medical Center, Haifa, Israel, “Effect of inorganic mercury on in vitro             placental nutrient transfer and oxygen consumption”, Reprod Toxicol, 1992,6(1):69-75;& ©  Karp W, Gale TF et al, Effect of mercuric acetate on selected enzymes of maternal and fetal hamsters” Environmental Research, 36:351-358; &  W.B. Karp et al, “Correlation of human placental enzymatic  activity with trace metal concentration in placenta”, Environ   Res. 13:470- 477,1977; & (d)  Boot JH.  Effects of SH‑blocking compounds on the energy metabolism and glucose uptake in isolated rat  hepatocytes.  Cell Struct Funct 1995 Jun;20(3):233‑8; &  Semczuk M, Semczuk‑Sikora A.  New data on toxic metal intoxication (Cd, Pb, and Hg in particular)  and Mg status during pregnancy.  Med Sci Monit 2001 Mar;7(2):332‑340; & (e) H.Iioka et al, “The effect of inorganic mercury on placental amino acid transport”, Nippon sanka Fujinka Gakkai Zasshi, 1987, 39(2): 202-6.

(16)  R.A.Goyer,”Toxic effects of metals”in: Caserett and Doull’s Toxicology- TheBasic Science of Poisons, McGraw-Hill Inc., N.Y., 1993; &(b) Goodman, Gillman, The Pharmacological Basis of Therapeutics, Mac Millan Publishing Company, N.Y. 1985; &(c) Encyclopedia of Occumpational Health and Safety, International Labour Office, Geneva, Vol 2, 3rd Edition.;&(d) Arena, Drew, Poisoning.  Fifth Edition.  Toxicology-Symptoms-Treatment, Charles C. Thomas-Publisher, Springfield, Il 1986

(17) Goyer RA, National Institute of Environmental Health Sciences.  Toxic and essential metal interactions.  Annu Rev Nutr 1997; 17:37-50; & Nutrition and metal toxicity.  Am J Clin Nutr 1995; 61(Suppl 3): 646S-650S;  & Lindh U, Carlmark B, Gronquist SO, Lindvall A. Metal exposure from amalgam alters the     distribution of trace  elements in blood cells and plasma.  Clin Chem Lab Med 2001 Feb;39(2):134‑142. ; & A.F.Goldberg et al, “Effect of Amalgam restorations on whole body potassium and bone mineral content in older men”,Gen Dent,         1996, 44(3): 246-8; & Knapp LT; Klann E.   Superoxide‑induced stimulation of protein kinase C via  thiol modification and modulation of zinc content. J Biol Chem 2000 May 22.

(18)  A.Badou et al, “HgCl2-induced IL-4 gene expression in T cells involves a protein kinase C-dependent calcium influx through L-type calcium channels”J Biol Chem. 1997 Dec 19;272(51):32411-8; & A.J.Freitas et al, “Effects of Hg2+ and CH3Hg+ on Ca2+ fluxes in the rat brain”,    Brain Research, 1996, 738(2): 257-64; & P.R.Yallapragoda et al,“Inhibition of calcium transport by Hg salts” in rat cerebellum and cerebral cortex”, J Appl toxicol, 1996, 164(4): 325-30;     & A. Szucs et al, Effects of inorganic mercury and methylmercury on the ionic currents of cultured rat hippocampal neurons. Cell Mol Neurobiol, 1997,17(3): 273-8; & D.Busselberg, 1995, “Calcium channels as target sites of heavy metals”,Toxicol Lett, Dec;82‑83:255‑61

(19) Lu SC, FASEB J, 1999, 13(10):1169‑83, “Regulation of hepatic glutathione synthesis: current concepts and controversies”;  & R.B. Parsons, J Hepatol, 1998, 29(4):595-602; &       R.K.Zalups et al,"Nephrotoxicity of inorganic mercury co‑administered with L‑cysteine", Toxicology, 1996, 109(1): 15‑29; & Wilkinson LJ, Waring RH.  Cysteine dioxygenase: modulation of expression in human cell lines by cytokines and control of sulphate production. Toxicol In Vitro. 2002 Aug;16(4):481-3

(20) C.Gordon et al, “Abnormal sulphur oxidation in systemic lupus erythrmatosus(SLE)”, Lancet,                 1992,339:8784,25-6; & P.Emory et al, “Poor sulphoxidation in patients with rheumatoid arthitis”,    

             Ann Rheum     Dis,  1992,  51:3,318-20; & Bradley H,et al,  Sulfate metabolism is abnormal in     patients with rheumatoid arthritis.  Confirmation by in vivo biochemical findings.  J Rheumatol. 1994     Jul;21(7):1192-6; & T.L. Perry et al,  Hallevorden-Spatz Disease: cysteine accumulation and cysteine    dioxygenase deficiency”, Ann Neural, 1985, 18(4):482-489.

(21) Chang LW, Hartmann HA,”Blood-brain barrier dysfunction in experimental mercury intoxication”.  Acta Neuropathol (Berl) 1972;21(3):179-84; & Ware RA, Chang LW, Burkholder PM,  “An Ultrastructural study on the blood-brain barrier dysfunction following mercury intoxication”,Acta Neurolpathol(Berlin), 1974,30(3): 211-214; & Prenatal and neonatal toxicology and pathology of heavy metals”  Adv Pharmacol Chemother., 1980, 17:195-231.

(22)  (a) Arvidson B; Arvidsson J; Johansson K, "Mercury Deposits in Neurons of the Trigeminal Ganglia After Insertion of Dental Amalgam in Rats", Biometals; 7 (3) p261-263 1994; & (b)Arvidson B. Inorganic mercury is transported from muscular nerve terminals to spinal and brainstem motorneurons.  Muscle Nerve 1992, 15:1089-94;. & (c) S.M. Candura et al, “Effects of mercuric chloride and methyl mercury on cholinergic neuromuscular transmission”, Pharmacol Toxicol 1997; 80(5): 218-24;

(23) Autism: a unique form of mercury poisoning.    http://www.autismwebsite.com/ari/vaccine/mercurylong.htm ; &  Green Bay News-Chronicle: Exposure to mercury linked to neurobehavioral disease epidemic in children, July 30, 2004, http://www.safeminds.org/pressroom/press_releases/30July2004-GreenBayNews.pdf & Breakthrough Research: New Columbia University Study Confirms IOM Vaccine-Autism Report Is Wrong, http://www.safeminds.org/pressroom/press_releases/14June2004_Hornig_Thimerosal_Mouse.pdf

& National Vaccine Information Center  http://www.909shot.com/

& (b) Elferink JG.  Thimerosal: a versatile sulfhydryl reagent, calcium mobilizer, and cell function‑ modulating agent.  Gen Pharmacol 1999 Jul;33(1):1‑6

(24) National Institute of Health,  NHANES III Study (National Health and Nutritional Examination Survey) http://www.mercola.com/article/mercury/no_mercury.htm

(25)  Case histories of autism/seizures in children treated by chelation for toxic metals,



(26) M. Daunderer,    Handbuch der Amalgamvergiftung, Ecomed Verlag, Landsberg 1998, ISBN 3‑609‑71750‑5 (in German); & “Improvement of Nerve and Immunological Damages after Amalgam Removal”, Amer. J. Of Probiotic Dentistry and Medicine, Jan 1991

(27) (a)A.F.Zamm, “Removal of dental mercury: often an effective treatment for very sensitive patients”, J Orthomolecular   Med, 1990, 5(53):138-142. (22 patients); & (b)Dr. T. Rau, Paracelsus Alergy Clinic, Lustmuhle,  Switzerland, Allergies: Causes, Clarification, Treatment; Explore, 8(4),1996, www.explorepub.com/articles/bio‑therapy.html

(28)  The Cure of All Diseases, Hulda Clark, New Century Press, 2002

(29) ) M.M. van Benschoten, ““Acupoint Energetics of Mercury Toxicity and Amalgam Removal with Case Studies,”” American Journal of Acupuncture, Vol. 22, No. 3, 1994, pp. 251-262; &  M.M. Van Benschoten  and Associates, Reseda, Calif.  Clinic; http://www.mmvbs.com/

(30) Autism Treatment Center,Baton Rouge, La, www.healing-arts.org/children/holmes.htm#wethink

& Metal-Metabolism and Autism:  Defective Functioning of Metallothionein Protein, Amy Holmes, MD;  http://www.healing-arts.org/children/metal-metabolism.htm


(38) Neurological effects of mercury toxicity, Review, B. Windham(Ed),


(39)  Immune and autoimmune effects of mercury exposure, Review, B.Windham (Ed),


(40)  Mechanisms by which mercury from dental amalgam is documented to cause over 30 chronic health conditions, and documentation of over 60,000 cases of recovery or significant health improvement from those conditions after amalgam replacement,

            B. Windham(Ed),  over 4,000 peer-reviewed or Gov’t studies cited,


(41) Life Enhancement Foundations (MDs), Disease Prevention and Treatment, Expanded Forth Edition, 2003 ,    http://www.life-enhancement.com/

(42) Overcoming Depression,  Dr. Russell Blaylock, The Blaylock Wellness Report, Vol 5, No. 3, March 2008, & Food Additives, What you eat can kill you, Vol 4, No. 10,  http://www.blaylockreport.com/



Dr. Ward Dean’s nutritional program for seizure disorders: He recommends using a nutritional "shotgun" therapy, which includes:




Hal Huggins(35) says he has a lot of clinical experience that mercury causes epilepsy and replacement often cures it. Others such as Dr. Noel Campbell, Dr. Hulda Clark(485), and ElectroDermal Screening testers with considerable clinical experience say likewise.


A Unique Type of
Mercury Poisoning

Sallie Bernard et al

Causes seizures, convulsions

Seizures; epilepsy

Causes subtle, low amplitude seizure activity



New research into the effects of mercury in Vaccin

es and links to Epilepsy are coming to light


Green Bay News-Chronicle: Exposure to mercury linked to neurobehavioral disease epidemic in children,
July 30, 2004, http://www.safeminds.org/pressroom/press_releases/30July2004-GreenBayNews.pdf

& Breakthrough Research: New Columbia University Study Confirms IOM Vaccine-Autism Report Is Wrong, http://www.safeminds.org/pressroom/press_releases/14June2004_Hornig_Thimerosal_Mouse.pdf


National Vaccine Information Center



Epilepsy Cure: Over 21 years ago, in June 1978, I started taking a large dose of the B Complex vitamins.
The dosage was 20mg. B 1,B 2 etc.;B 12 20mcg and folic acid at 400mcg. I immediately felt more energetic and alive. I had grand mal epilepsy for the prior 25 years, since I had entered puberty at age 13. In those days 20 mg was probably a megadose, I'm not sure, today I take 50mg. because its more commonly available. I had been taking anticonvulsant medication trade name Mebroin including Phenobarbital and a smaller amount of Dilantin. I was able to wean my way off the anticonvulsant medication in July of 1978. I have not taken any medication since, and have become a new person



A study published in the New England Journal of Medicine examined newborns for birth defects related to anticonvulsant drugs. Each newborn belonged to one of three groups: newborns exposed to anticonvulsant drugs in the womb; newborns of mothers with epilepsy who did not take anticonvulsant drugs; and newborns of mothers without epilepsy or a history of seizures. Results showed birth defects were more frequent in infants exposed to anticonvulsant drugs (20% of infants exposed to one drug had birth defects and 28% of infants exposed to two or more drugs had birth defects). However, the infants of mothers with epilepsy who were not treated with anticonvulsant drugs were at no greater risk of birth defects then infants of mothers without epilepsy.

Harvard Medical School Family Health Guide


This study suggests birth defects are caused by anticonvulsant drugs and not by epilepsy itself. A separate, earlier study based on data from a number of different countries identified the types of birth defects associated with common anticonvulsant drugs. Some of these findings are summarized below:


Side Effect Warning for New Rheumatoid Arthritis Drug, Remicade (Infliximab)
All drugs have side effects, but some of them don't become apparent until after the drugs have been approved and in use for some time.

Remicade (infliximab), a powerful new drug for rheumatoid arthritis, has been found to worsen congestive heart failure. The drug was actually being tested to see if it would help patients with congestive heart failure. Instead, the opposite was seen in a trial involving 150 people with moderate to severe congestive heart failure. Of the 101 subjects treated with Remicade, 7 died. In contrast, no fatalities occurred in the 49 patients being treated with the sugar pill placebo.

Some 2 million Americans suffer from rheumatoid arthritis, while 5 million have congestive heart failure. So an undetermined number must have both illnesses. As a result, Centocor, the company making Remicade, after consultation with the U.S. Food and Drug Administration, has sent letters to doctors urging that patients with both rheumatoid arthritis and congestive heart failure not be treated with their drug.
November 2001 Update

This new information, comes straight from the National Institute of Health, the NHANES III Study (National Health and Nutritional Examination Survey), a study that according to the mission statement of National Center for Health Sciences "is to provide statistical information that will guide the actions and policies to improve health of the American people. As the Nation's principal health statistics agency, NCHS leads the way with accurate, relevant, and timely data."

A recent statistical analysis of this data was done to see if there were any links to dental fillings and adverse health conditions.

Their initial figures revealed that while 78% of the American public have dental fillings, 95% of the people with International Classification of Disease Codes 340-349: "Disorders of the Central Nervous System", which include MS, Epilepsy, Paralysis and Migraines, have dental fillings.

National Institute of Health,  NHANES III Study (National Health and Nutritional Examination Survey) http://www.mercola.com/article/mercury/no_mercury.htm


Prenatal Mercury Exposure Raises Blood Pressure  


Exposure to mercury before birth may lead to increased blood pressure in childhood, reports an international team of researchers. The islanders consume a diet rich in marine products, such as pilot whale meat, which expose them to mercury, according to the investigators. Blood pressures increased by about 14 points as blood mercury concentrations at birth increased from 1 to 10 micrograms per liter. The report indicates that 10 micrograms per liter corresponds to the upper limit of mercury exposure recommended by the German Commission on Human Biomonitoring, indicating that blood pressure can be increased by exposure to mercury levels below recommended limits. Children with lower birth weights experienced blood pressure increases about 50% higher than normal birth weight children having similar mercury levels. The investigators cite evidence that mercury toxicity can cause high blood pressure that persists long after the mercury exposure has been removed, resulting in a significant risk for diseases such as heart attack and stroke.

Epidemiology   July 1999;10:370-375

the prestigious New England Journal of Medicine published an editorial (12 ) calling mercury fillings the chief source of mercury exposure to the US population


Salonen JT, Nyyssonen K, Salonen R. Fish intake and the risk of coronary disease. N Engl J Med. 1995 Oct 5;333(14):937


Effects of continuous low-dose exposure to organic and inorganic mercury during development on epileptogenicity in rats.

Szasz A, Barna B, Gajda Z, Galbacs G, Kirsch-Volders M, Szente M.  Neurotoxicology. 2002 Jul;23(2):197-206.

Department of Comparative Physiology, University of Szeged, Hungary. szente@bio.u-szeged.hu

The effects of chronic, low-dose fetal and lactational organic (MeHgCl) and inorganic (HgCl2) mercury intoxication on epileptogenicity were investigated and compared in rats. The main observations after both mercury treatments were a facilitated seizure expression and propagation evoked by 4-aminopyridine (4-AP). The seizure susceptibility of the offspring seemed to be in a parallel relation to the mercury concentration in the cortical tissue, which was significantly higher in treated animals as compared to the controls. While MeHgCl enhanced the number of ictal periods, HgCl2 facilitated the duration of seizure discharges in younger animals. HgCl2 intoxication seemed to be more permanent than MeHgCl. Changes in the summated ictal activity--which is an indication of epileptogenicity--were observed in the opposite directions in the two treated groups with increasing age. The amplitudes of seizure discharges were smaller in both mercury-treated groups than in the controls, which could be a consequence of a depressed proliferation of neurons or enhanced cell death in the neocortex. In summary, we observed that adult rats exposed to organic or inorganic mercury chemicals during their embryonic life, are more prone to epilepsy than control rats given only 4-AP.



From: Verstraeten, Thomas,  U.S. CDC

Sent: Monday, November 29, 1999 11:45 AM



The results of the Generation Zero analyses are striking and more supportive of a causal relationship

between vaccine mercury exposure and childhood developmental disorders (especially autism) than

any of the results reported later

Relative risks of autism, ADD, sleep disorders and speech/language delay were consistently

elevated relative to other disorders and frequently significant. Disease risk for the high

exposure groups ranged from lows of 1.5X-2 times to as high as 11 times the disease risk of

the zero exposure group.

Many other outcomes showed no consistent effect, while a few appeared to show a

protective effect from vaccine mercury exposure (most likely children with these diagnoses

were immunized later).

The strongest effect was for the highest levels of mercury exposure at the earliest time of

exposure, consistent with the idea that infant brain development is most sensitive to the

earliest exposures.

The elevated risk of autism for the highest exposure levels at one month ranged from 7.6 to

11.4 times the zero exposure level. This increased risk level corresponds to the tenfold

increase in autism rates seen since vaccine mercury exposures increase starting in 1990.

Diagnoses with elevated risks

399.0 Autism

307.0 Stammering

307.2 Tics

• 307.20, tic disorder, unspecified

307.4 Specific disorders of sleep of non-organic

• 307.45, phase shift disruption of 24 hr. sleepwake


• 307.46, somnambulism or night terrors

314.0 Attention deficit disorder

• 314.00, ADD without mention of hyperactivity

• 314.01 ADD with hyperactivity

315.3 Developmental speech or language disorder

• 315.31, developmental language disorder

• 315.39, other developmental speech or language


315.4 Coordination disorder

583 Nephritis and nephropathy, not acute or chronic

• 583.9 nephritis and nephropathy, with

unspecified pathological lesion in kidney