What neurotoxicity looks like ... as demonstrated by a mouse after mild exposure to new, synthetic carpet. Testing done by Anderson Laboratories. Feel bad for the mouse? We are doing much worse to ourselves all the time without noticing. Symptomology has become normalized. Doctors are not trained in toxicology. Chemicals are not proven safe before brought to market. Cancer is easier to prevent than cure (stop using carcinogens). Restore logic. Listen to Antidote Radio (antidoteradio.com), peruse sites such as scorecard.org, toxgun.com, ewg.org, drrapp.com, neurotox.com, and do your own research. Do you really have a mood disorder? Start noticing how exposures affect you. Even a bunch of EPA employees got sick from new carpet, which is linked to symptoms and disorders of many kinds. Chemicals are a trillion dollar industry. Ignore industry PR. Listen to canaries (and mice).

Howard S. Hochster, M.D., NYU Cancer Center http://www.medpagetoday.com ORLANDO -- The warning that emerged a year ago that adding IV calcium and magnesium to therapy with oxaliplatin (Eloxatin) counteracted the drug's efficacy in metastatic colorectal cancer appears to have been a false alarm.

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On October 24, 1996 Dr. Phyllis Mullenix spoke about fluoride at Clark University in Worchester, Massachusetts. For more information on fluoride and water fluoridation visit the website www.MaeBrussell.com. Go to the "Articles, excerpts, and notes" section.

Pharmacology: Methamphetamine is a potent central nervous system stimulant which affects neurochemical mechanisms responsible for regulating heart rate, body temperature, blood pressure, appetite, attention, mood and responses associated with alertness or alarm conditions. The acute effects of the drug closely resemble the physiological and psychological effects of an epinephrine-provoked fight-or-flight response, including increased heart rate and blood pressure, vasoconstriction (constriction of the arterial walls), bronchodilation, and hyperglycemia (increased blood sugar). Users experience an increase in focus, increased mental alertness, and the elimination of fatigue, as well as a decrease in appetite. The methyl group is responsible for the potentiation of effects as compared to the related compound amphetamine, rendering the substance on the one hand more lipid soluble and easing transport across the blood brain barrier, and on the other hand more stable against enzymatic degradation by MAO. Methamphetamine causes the norepinephrine, dopamine and serotonin(5HT) transporters to reverse their direction of flow. This inversion leads to a release of these transmitters from the vesicles to the cytoplasm and from the cytoplasm to the synapse (releasing monoamines in rats with ratios of about NE:DA = 1:2, NE:5HT= 1:60), causing increased stimulation of post-synaptic receptors. Methamphetamine also indirectly prevents the reuptake of these neurotransmitters, causing them to remain in the synaptic cleft for a prolonged period (inhibiting monoamine reuptake in rats with ratios of about: NE:DA = 1:2.35, NE:5HT = 1:44.5). Methamphetamine is a potent neurotoxin, shown to cause dopaminergic degeneration. High doses of methamphetamine produce losses in several markers of brain dopamine and serotonin neurons. Dopamine and serotonin concentrations, dopamine and 5HT uptake sites, and tyrosine and tryptophan hydroxylase activities are reduced after the administration of methamphetamine. It has been proposed that dopamine plays a role in methamphetamine induced neurotoxicity because experiments which reduce dopamine production or block the release of dopamine decrease the toxic effects of methamphetamine administration. When dopamine breaks down it produces reactive oxygen species such as hydrogen peroxide. It is likely that the oxidative stress that occurs after taking methamphetamine mediates its neurotoxicity. It has been demonstrated that a high ambient temperature increases the neurotoxic effects of methamphetamine. Recent research published in the Journal of Pharmacology And Experimental Therapeutics (2007), indicates that methamphetamine binds to a group of receptors called TAAR. TAAR is a newly discovered receptor system which seems to be affected by a range of amphetamine-like substances called trace amines.

Be My Friend - http://www.myspace.com/psychtruth The Truth about MSG Monosodium Glutamate Clinical Nutrition What effects does MSG have on diet, obesity, health and food cravings? Because MSG is absorbed very quickly in the gastrointestinal tract (unlike glutamic acid-containing proteins in foods), MSG could spike blood plasma levels of glutamate. Glutamic acid is in a class of chemicals known as excitotoxins, high levels of which have been shown in animal studies to cause damage to areas of the brain unprotected by the blood-brain barrier and that a variety of chronic diseases can arise out of this neurotoxicity. Dr. Vincent Bellonzi is a chiropractor and a Certified Clinical Nutritionist. He has been in practice for over 12 years. He received his Doctorate from Los Angeles College of Chiropractic in 1991. Since 1998, Dr. Bellonzi has practiced in the Austin area. He works with athletes at every level to provide sports conditioning and rehabilitation. Visit Dr. Bellonzi's website at http://www.bewellrx.com http://www.austinwellnessinstitute.com This video was produced by Psychetruth http://www.myspace.com/psychtruth http://www.youtube.com/psychetruth © Copyright 2007 Austin Wellness Institute. All Rights Reserved.

Do you think vaccines are safe? According to neurosurgeon Dr. Russell Blaylock, people who get the flu shot five years in a row have a ten-fold increased risk of developing Alzheimer's. The flu vaccine still has the full amount of ethyl mercury, contained in the preservative thimerosal. This video from the University of Calgary shows the death of brain cells after their exposure to mercury. The neurotoxicity of mercury is a fact that is not disputed. Neurodegenerative diseases include Alzheimer's, Parkinson's, Huntington's and Amyotrophic Lateral Sclerosis (ALS), or Lou Gehrig's Disease. Would you rather have one of those, or the flu?! For more info, visit my blog: Red Pill Reich http://redpillreich.blogspot.com/ I am a nurse who is exposing the Illuminati's use of modern medicine to drug, poison and control millions in their pursuit of a New World Order.

Ecstasy - Do not let the name fool you (2004); Anti Ecstasy film produced by US Navy; Producer: US Navy; Keywords: drugs; abuse; PSA; Contact Information: http://navdweb.spawar.navy.mil/ecstasy.asp Creative Commons license: Attribution-NonCommercial-NoDerivs. MDMA (3,4 methylenedioxymethamphetamine) is a synthetic, psychoactive drug chemically similar to the stimulant methamphetamine and the hallucinogen mescaline. Street names for MDMA include Ecstasy, Adam, XTC, hug, beans, and love drug. MDMA is an illegal drug that acts as both a stimulant and psychedelic, producing an energizing effect, as well as distortions in time and perception and enhanced enjoyment from tactile experiences. MDMA exerts its primary effects in the brain on neurons that use the chemical serotonin to communicate with other neurons. The serotonin system plays an important role in regulating mood, aggression, sexual activity, sleep, and sensitivity to pain. Research in animals indicates that MDMA is neurotoxic; whether or not this is also true in humans is currently an area of intense investigation. MDMA can also be dangerous to health and, on rare occasions, lethal. Health Hazards: For some people, MDMA can be addictive. A survey of young adult and adolescent MDMA users found that 43 percent of those who reported ecstasy use met the accepted diagnostic criteria for dependence, as evidenced by continued use despite knowledge of physical or psychological harm, withdrawal effects, and tolerance (or diminished response), and 34 percent met the criteria for drug abuse. Almost 60 percent of people who use MDMA report withdrawal symptoms, including fatigue, loss of appetite, depressed feelings, and trouble concentrating. Cognitive Effects: Chronic users of MDMA perform more poorly than nonusers on certain types of cognitive or memory tasks. Some of these effects may be due to the use of other drugs in combination with MDMA, among other factors. Physical Effects: In high doses, MDMA can interfere with the body's ability to regulate temperature. On rare but unpredictable occasions, this can lead to a sharp increase in body temperature (hyperthermia), resulting in liver, kidney, and cardiovascular system failure, and death. Because MDMA can interfere with its own metabolism (breakdown within the body), potentially harmful levels can be reached by repeated drug use within short intervals. Users of MDMA face many of the same risks as users of other stimulants such as cocaine and amphetamines. These include increases in heart rate and blood pressure, a special risk for people with circulatory problems or heart disease, and other symptoms such as muscle tension, involuntary teeth clenching, nausea, blurred vision, faintness, and chills or sweating. Psychological Effects: These can include confusion, depression, sleep problems, drug craving, and severe anxiety. These problems can occur during and sometimes days or weeks after taking MDMA. Neurotoxicity: Research in animals links MDMA exposure to long-term damage to neurons that are involved in mood, thinking, and judgment. A study in nonhuman primates showed that exposure to MDMA for only 4 days caused damage to serotonin nerve terminals that was evident 6 to 7 years later. While similar neurotoxicity has not been definitively shown in humans, the wealth of animal research indicating MDMA's damaging properties suggests that MDMA is not a safe drug for human consumption. Hidden Risk: Drug Purity - Other drugs chemically similar to MDMA, such as MDA (methylenedioxyamphetamine, the parent drug of MDMA) and PMA (paramethoxyamphetamine, associated with fatalities in the U.S. and Australia) are sometimes sold as ecstasy. These drugs can be neurotoxic or create additional health risks to the user. Also, ecstasy tablets may contain other substances in addition to MDMA, such as ephedrine (a stimulant); dextromethorphan (DXM, a cough suppressant that has PCP-like effects at high doses); ketamine (an anesthetic used mostly by veterinarians that also has PCP-like effects); caffeine; cocaine; and methamphetamine. While the combination of MDMA with one or more of these drugs may be inherently dangerous, users might also combine them with substances such as marijuana and alcohol, putting themselves at further physical risk.

4 Anti Ecstasy Public Service Spots from US Navy. MDMA (3,4 methylenedioxymethamphetamine) is a synthetic, psychoactive drug chemically similar to the stimulant methamphetamine and the hallucinogen mescaline. Street names for MDMA include Ecstasy, Adam, XTC, hug, beans, and love drug. MDMA is an illegal drug that acts as both a stimulant and psychedelic, producing an energizing effect, as well as distortions in time and perception and enhanced enjoyment from tactile experiences. MDMA exerts its primary effects in the brain on neurons that use the chemical serotonin to communicate with other neurons. The serotonin system plays an important role in regulating mood, aggression, sexual activity, sleep, and sensitivity to pain. Research in animals indicates that MDMA is neurotoxic; whether or not this is also true in humans is currently an area of intense investigation. MDMA can also be dangerous to health and, on rare occasions, lethal. Health Hazards: For some people, MDMA can be addictive. A survey of young adult and adolescent MDMA users found that 43 percent of those who reported ecstasy use met the accepted diagnostic criteria for dependence, as evidenced by continued use despite knowledge of physical or psychological harm, withdrawal effects, and tolerance (or diminished response), and 34 percent met the criteria for drug abuse. Almost 60 percent of people who use MDMA report withdrawal symptoms, including fatigue, loss of appetite, depressed feelings, and trouble concentrating. Cognitive Effects: Chronic users of MDMA perform more poorly than nonusers on certain types of cognitive or memory tasks. Some of these effects may be due to the use of other drugs in combination with MDMA, among other factors. Physical Effects: In high doses, MDMA can interfere with the body's ability to regulate temperature. On rare but unpredictable occasions, this can lead to a sharp increase in body temperature (hyperthermia), resulting in liver, kidney, and cardiovascular system failure, and death. Because MDMA can interfere with its own metabolism (breakdown within the body), potentially harmful levels can be reached by repeated drug use within short intervals. Users of MDMA face many of the same risks as users of other stimulants such as cocaine and amphetamines. These include increases in heart rate and blood pressure, a special risk for people with circulatory problems or heart disease, and other symptoms such as muscle tension, involuntary teeth clenching, nausea, blurred vision, faintness, and chills or sweating. Psychological Effects: These can include confusion, depression, sleep problems, drug craving, and severe anxiety. These problems can occur during and sometimes days or weeks after taking MDMA. Neurotoxicity: Research in animals links MDMA exposure to long-term damage to neurons that are involved in mood, thinking, and judgment. A study in nonhuman primates showed that exposure to MDMA for only 4 days caused damage to serotonin nerve terminals that was evident 6 to 7 years later. While similar neurotoxicity has not been definitively shown in humans, the wealth of animal research indicating MDMA's damaging properties suggests that MDMA is not a safe drug for human consumption. Hidden Risk: Drug Purity - Other drugs chemically similar to MDMA, such as MDA (methylenedioxyamphetamine, the parent drug of MDMA) and PMA (paramethoxyamphetamine, associated with fatalities in the U.S. and Australia) are sometimes sold as ecstasy. These drugs can be neurotoxic or create additional health risks to the user. Also, ecstasy tablets may contain other substances in addition to MDMA, such as ephedrine (a stimulant); dextromethorphan (DXM, a cough suppressant that has PCP-like effects at high doses); ketamine (an anesthetic used mostly by veterinarians that also has PCP-like effects); caffeine; cocaine; and methamphetamine. While the combination of MDMA with one or more of these drugs may be inherently dangerous, users might also combine them with substances such as marijuana and alcohol, putting themselves at further physical risk. Producer: US NAVY Production Company: http://navdweb.spawar.navy.mil/fr_index.html?/ecstasy.asp Creative Commons license: Attribution-NonCommercial-NoDerivs

DigInfo - (http://movie.diginfo.tv) A team from the Laboratory for Proteolytic Neuroscience at RIKEN is conducting various research on Alzheimer's disease especially in the study of somatostatin, a neuropeptide that inhibits the secretion of growth hormone and could lead to the discovery of new medicines for Alzheimer's disease. Alzheimer's disease is a cognitive dysfunction disorder that occurs when nerve cells are impaired and the brain becomes spongy.　There are around 24 million Alzheimer patients worldwide. Amyloid β peptide has been identified as the pathogen that exhibits neurotoxicity and consists of 42 amino acids which are produced in the brain. Alzheimer's disease occurs when amyloidsβ-peptides accumulate in excess outside of the nerve cells. The Researchers at Riken also discovered that Neprilysin, which breaks up amyloidβ- peptide, diminishes with age and decreases even further upon the onset of Alzheimer's disease. In the laboratory, they treated an Alzheimer's disease model mouse with a gene therapy that boosted the activity of Neprilysin by 10 times, and as a result, were able to suppress the accumulation of the amyloid β- peptide. Somatostatin can act to reinforce memory retention, so it has the potential to be both a treatment and preventive drug for Alzheimer's disease. RIKEN is currently conducting bio-chemical and histological analysis of the brain using an Alzheimer's disease model mouse.

Video of little Megan Leslie who has autism.

Symptoms Heavy Metal Poisoning back Pain Anger Adrenaline Neurotoxicity Mercury Aluminium Cadmium Lead Arsenic Uranium Tungsten Tin Thorium Thallium Platinum Nickel Bismuth Beryllium Antimony

The people who brought you: Thalidomide, Vioxx, Avandia, Aspartame, Orobilix. Birth Defects no limbs, Autism, Deaths, Cancer,Neurotoxicity Morbidity and Mortality

Click 'more' for details. The information below is an excerpt from the library on the Norml web site. Please excuse Spelling Error on video Open! Typing with one hand here, found mistake after! Click the link down below to see the text in full, complete with references. A review of the recent scientific literature indicates that cannabinoid therapy may provide symptomatic relief to patients afflicted with AD while also moderating the progression of the disease. Writing in the February 2005 issue of the Journal of Neuroscience, investigators at Madrid's Complutense University and the Cajal Institute in Spain reported that the intracerebroventricular administration of the synthetic cannabinoid WIN 55,212-2 prevented cognitive impairment and decreased neurotoxicity in rats injected with amyloid-beta peptide (a protein believed to induce Alzheimer's). Additional cannabinoids were also found to reduce the inflammation associated with Alzheimer's disease in human brain tissue in culture. "Our results indicate that ... cannabinoids succeed in preventing the neurodegenerative process occurring in the disease," investigators concluded.[1] Investigators at The Scripps Research Institute in California in 2006 reported that THC inhibits the enzyme responsible for the aggregation of amyloid plaque — the primary marker for Alzheimer's disease — in a manner "considerably superior" to approved Alzheimer's drugs such as donepezil and tacrine. "Our results provide a mechanism whereby the THC molecule can directly impact Alzheimer's disease pathology," researchers concluded. "THC and its analogues may provide an improved therapeutic [option] for Alzheimer's disease [by]... simultaneously treating both the symptoms and the progression of [the] disease."[2] Most recently, investigators at Ohio State University, Department of Psychology and Neuroscience, reported that older rats administered daily doses of WIN 55,212-2 for a period of three weeks performed significantly better than non-treated controls on a water-maze memory test. Writing in the journal Neuroscience in 2007, researchers reported that rats treated with the compound experienced a 50 percent improvement in memory and a 40 to 50 percent reduction in inflammation compared to controls.[3] Full Text Link: http://www.norml.org/index.cfm?Group_ID=7003 The Author on the Norml Site: For patients and their physicians, let this report serve as a primer for those who are considering using or recommending medicinal cannabis. For others, let this report serve as an introduction to the broad range of emerging clinical applications for cannabis and its various compounds. Paul Armentano Deputy Director NORML | NORML Foundation Washington, DC January 24, 2008 * The author would like to acknowledge Drs. Dale Gieringer, Gregory Carter, Steven Karch, and Mitch Earleywine, as well as NORML interns John Lucy, Christopher Rasmussen, and Rita Bowles, for providing research assistance for this report. The NORML Foundation would also like to acknowledge Dale Gieringer, Paul Kuhn, and Richard Wolfe for their financial contributions toward the publication of this report. ** Important and timely publications such as this are only made possible when concerned citizens become involved with NORML. For more information on joining NORML or making a donation, please visit: http://www.norml.org/join. Tax deductible donations in support of NORML's public education campaigns should be made payable to the NORML Foundation. ___________________________________ "Prohibition...goes beyond the bounds of reason in that it attempts to control a man's appetite by legislation and makes a crime out of things that are not crimes. A prohibition law strikes a blow at the very principles upon which our government was founded." -- Abraham Lincoln December 1840

Dr. B.J. Hardick of the Maximized Living Makeover teaches why some people lose weight using traditional weight loss programs, while others do not. Learn about your customized program for weight loss to overcome challenges with the hormone Leptin and with neurotoxicity at Dr. Hardick's next seminar. www.MaximizedLivingDrHardick.com

Ecstasy Video. Ecstasy: What's all the Rave About?. Public Service Announcement and public domain video from U.S. Department of Health and Human Services Substance Abuse and Mental Health Services Administration. MDMA (3,4 methylenedioxymethamphetamine) is a synthetic, psychoactive drug chemically similar to the stimulant methamphetamine and the hallucinogen mescaline. Street names for MDMA include Ecstasy, Adam, XTC, hug, beans, and love drug. MDMA is an illegal drug that acts as both a stimulant and psychedelic, producing an energizing effect, as well as distortions in time and perception and enhanced enjoyment from tactile experiences. MDMA exerts its primary effects in the brain on neurons that use the chemical serotonin to communicate with other neurons. The serotonin system plays an important role in regulating mood, aggression, sexual activity, sleep, and sensitivity to pain. Research in animals indicates that MDMA is neurotoxic; whether or not this is also true in humans is currently an area of intense investigation. MDMA can also be dangerous to health and, on rare occasions, lethal. What does it look like? Ecstasy comes in a tablet form that is often branded, e.g. Playboy bunnies, Nike swoosh, CK. How is it used? Taken in pill form, users sometimes take Ecstasy at "raves," clubs and other parties to keep on dancing and for mood enhancement. What are its short-term effects? Users report that Ecstasy produces intensely pleasurable effects -- including an enhanced sense of self-confidence and energy. Effects include feelings of peacefulness, acceptance and empathy. Users say they experience feelings of closeness with others and a desire to touch others. Other effects can include involuntary teeth clenching, a loss of inhibitions, transfixion on sights and sounds, nausea, blurred vision, chills and/or sweating. Increases in heart rate and blood pressure, as well as seizures, are also possible. The stimulant effects of the drug enable users to dance for extended periods, which when combined with the hot crowded conditions usually found at raves, can lead to severe dehydration and hyperthermia or dramatic increases in body temperature. This can lead to muscle breakdown and kidney, liver and cardiovascular failure. Cardiovascular failure has been reported in some of the Ecstasy-related fatalities. After-effects also include sleep problems, anxiety and depression. What are its long-term effects?Repeated use of Ecstasy ultimately may damage the cells that produce serotonin, which has an important role in the regulation of mood, appetite, pain, learning and memory. There already is research suggesting Ecstasy use can disrupt or interfere with memory. What is its federal classification? Schedule I. For some people, MDMA can be addictive. A survey of young adult and adolescent MDMA users found that 43 percent of those who reported ecstasy use met the accepted diagnostic criteria for dependence, as evidenced by continued use despite knowledge of physical or psychological harm, withdrawal effects, and tolerance (or diminished response), and 34 percent met the criteria for drug abuse. Almost 60 percent of people who use MDMA report withdrawal symptoms, including fatigue, loss of appetite, depressed feelings, and trouble concentrating. Chronic users of MDMA perform more poorly than nonusers on certain types of cognitive or memory tasks. Some of these effects may be due to the use of other drugs in combination with MDMA, among other factors. These can include confusion, depression, sleep problems, drug craving, and severe anxiety. These problems can occur during and sometimes days or weeks after taking MDMA. Research in animals links MDMA exposure to long-term damage to neurons that are involved in mood, thinking, and judgment. A study in nonhuman primates showed that exposure to MDMA for only 4 days caused damage to serotonin nerve terminals that was evident 6 to 7 years later. While similar neurotoxicity has not been definitively shown in humans, the wealth of animal research indicating MDMA's damaging properties suggests that MDMA is not a safe drug for human consumption.

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To much cake! All the respect for the fanbase around the game Portal. Most of the art is taken from DeviantArt. Credits for the great game goes to Valve. Rest of the credits belong to me and Fruityloops.

I did not edit or produce this video. I only uploaded it. To see scientific experiments on how rats get cancer caused by Aspartame go here: http://myaspartameexperiment.com http://www.foodnavigator-usa.com/Financial-Industry/New-natural-sweetener-claims-1-1-sugar-replacement THER NATURAL ALTERNATIVE - STEVIA! 1000 TIME MORE SWEETER THAN SUGAR! No it is not new - natives have been using it for thousands of years, only dumb Americans think it is something new. http://www.slashfood.com/2006/08/16/stevia-gains-popularity-as-a-sweetener/ Stevia is not a sweetener that is approved for use by the FDA. It is actually classified as a dietary supplement, an herb, that happens to be sweeter than sugar and can be - and is - used as a sweetener. It is all natural, has no calories (or carbs) and is getting more and more popular, though it makes up only a small portion of the non-sugar sweetener market. SAY NO TO MONSANTO'S FRANKENSTIEN CREATION! THEIR NEUROTOXIC POISON! STOP BUYING ANY PRODUCT THAT CONTAINS IT IS AN INGREDIENT! THAT IS 99.9% OF ALL CHILDRENS FOOD AND DRINKS! THEY WANT YOU AND YOUR KIDS DUMB, THEY WANT YOU ALL BRAINDEAD. WILL YOU BE THEIR GOOD LITTLE SLAVES! OR BOYCOTT THEM ALL. JUST LIKE I DO EVERY DAY OF MY LIFE. If you still want a a sweetener then use Ogranic Stevia that is natural and 1000 times more sweet than sugar! http://www.google.com/search?hl=en&q=organic+stevia+sweetener+1000+times+sweeter+than+cane+sugar&btnG=Search&meta= Aspartame Dumbing Down, Poison, Monsanto, Searle, Rumsfeld Aspartame is genetically engineered but not labeled as such any any country in the world to my knowledge, not even in European Union countries where the law sstates all food containing GMO ingredients must be laballed as such. This is because the final product is not meant to contain any genetically modified materials. This does not make me happy or hundreds of millions of other people happy about this statement either! We want it out our food and GM food banned! Monsanto held to rights for war crimes against humanity and nature! Try researching Fluoride while you are at it, the Nazis first came up with the idea of using phosphates of fertilizers, aluminium fluorides, fluoride of the chemical waste from industry is used to poison you and once you have been on it for so long it restructures your brain irreversibly. Once again people it was the Nazis that first developed it and used it in their concentration camps to dumb down their slaves! America not only funded WWII in which you will find is true in declassified documents, the CIA were actually founded by Nazi war criminals at the war end. And this was because the FBI had recruited Nazi war criminals into America (mostly scientists) under the operation paperclip. Do some research if not done already. http://www.amazon.com/Secret-Relationship-Between-Blacks-Jews/dp/0963687700 http://en.wikipedia.org/wiki/Operation_paperclip New World Order Police State One World Order Government CIA WAS FORMED BY NAZIS! AND USING THEM AS EMPLOYEES! AND THEIR TECHNOLOGY. THEY WENT ON TO EXPERIMENT ON AMERICANS! NOW THE WHOLE WORLD! YET PEOPLE ARE BLIND TO ALL OF THIS! http://emperors-clothes.com/analysis/gehlen.htm http://www.democraticunderground.com/discuss/duboard.php?az=show_mesg&forum=389&topic_id=2596898&mesg_id=2605811 Go to above links to see the kind of world we live in, who really has control for their masters. Why not try independently using your BRAIN! If you have one that is of your own! And also research how the European Union was formed, look up the original name of the European Union which when translated from what Adolf Hitler names NEU EUROPA - European Economic Community or Europäischen Wirtschaftsgemeinschaft in German. You are living the Nazi dream! All European countries have lost their sovereignty, all major EU Institutions are based in GERMANY! Everyone is so dumb though they do not care or even notice. Some people are aware of this though: http://boards.virginmedia.com/news/soundbites/20080922_darling_pledge_over_economic_crisis.html?page=15 The Nazis WON! http://www.europeansinglecurrency.com/euro%20and%20USE.htm

This is one heck of a serious topic and Underground Wellness gives it a go. If you drink tap water think again. If you have children think even harder about the known neurotoxic effects of one of the aluminium industries waste / externalities. Arent teeth maintained by a healthy diet and functioning immune system?? If so then why would ingesting a rather high on the periodic table element trump diet and lifestyle?? This information is to inform you on nutrition matters. It is not intended to make any suggestions regarding medicine, pharmaceutical drugs, or give medical advice. Do your research and consult your doctor. This video has be rebroadcast with permission from Under Ground Wellness @ http://www.youtube.com/user/undergroundwellness Whey protein supplements diet recovery nutrition disease health flouride water supply privatization

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