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Pictures, Dr. Alemany who did the Trocho Study, Corinne Gouget, Mission Possible France and Dr. Betty Martini, D.Hum - Resolution to ban in English and French

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Everyone should get involved and can use this

resolution in states and countries. We will help

in any way we can. Dr. M. Alemany is the

courageous researcher who did the damning Trocho

Study. NutraSweet tried to assassinate his

character and research funds were reduced. He

said aspartame can kill 200 million people.

 

Dr. Betty Martini, D.Hum, Founder

Mission Possible International

9270 River Club Parkway

Duluth, Georgia 30097

770 242-2599

www.mpwhi.com, www.dorway.com and www.wnho.net

Aspartame Toxicity Center, www.holisticmed.com/aspartame

 

 

><http://www.santeendanger.net>www.santeendanger.net

>

>Corinne

>

>

>

>

>Début du message réexpédié :

>

>>De : Corinne GOUGET

>><<missionpossible.francemissionpossible.france

>>Date : 19 septembre 2008 13:28:40 HAEC

>>À : <finrodfinrod

>>Objet : Réexp : IMPORTANT MESSAGE from Corinne GOUGET

>>

>>Resolution in English then in French:

>>

>>RESOLUTION

>>

>>

>>REQUESTING THE DEPARTMENT OF HEALTH TO REVIEW EXISTING REPORTS

>>AND STUDIES RELATED TO ASPARTAME, AND REQUESTING THE MINISTRY OF

>>HEALTH IN THIS RESPECTIVE COUNTRY TO RESCIND APPROVAL OF ASPARTAME

>>FOR SALE TO THE PUBLIC IN THE MARKETS OF THIS COUNTRY.

>>

>>

>> WHEREAS, aspartame was originally developed as a drug to treat peptic

>>ulcers; and

>>

>>

>>

>> WHEREAS, manufacturers state that aspartame is made up of forty per

>>cent aspartic acid, fifty per cent phenylalanine, and ten per cent methanol;

>>and

>>

>>

>>

>> WHEREAS, aspartic acid is a nonessential amino acid that is used by the

>>body to initiate apoptosis or cell death in aging cells, and that excess

>>aspartic acid from aspartame consumption causes apoptosis in healthy cells

>>that can destroy healthy tissue, especially in the brain; and

>>

>>

>>

>> WHEREAS, phenylalanine is an essential amino acid found naturally in

>>protein but when isolated becomes neurotoxic, lowers the seizure threshold,

>>depletes serotonin triggering psychiatric and behavioral problems, and

>>interacts with antidepressants and other drugs; and

>>

>>

>>

>> WHEREAS, methanol is a severe metabolic poison classified as a narcotic

>>that converts to formaldehyde and formic acid, and can embalm living tissue

>>and damage DNA; and

>>

>>

>>

>> WHEREAS, aspartame metabolites include formaldehyde, a " class A "

>>carcinogen, diketopiperazine, a brain tumor agent, and formic acid; and

>>

>>

>>

>> WHEREAS, in 1974, the United States Food and Drug Administration

>>approved aspartame as an artificial sweetener, but asked its manufacturer

>>Searle to hold back from selling it on the market until further tests could

>>be made with regards to its safety; and

>>

>>

>>

>> WHEREAS, scientific data revealed that there was a problem with

>>aspartame safety data and the United States Food and Drug Administration

>>withdrew its approval; and

>>

>>

>>

>> WHEREAS, in 1975, the United States Food and Drug Administration

>>initiated an investigation into Searle's laboratory practices and discovered

>>fraud in scientific experiments as well as manipulated data giving favorable

>>results proving aspartame to be safe; and

>>

>>

>>

>> WHEREAS, the results of this investigation are included in what is

>>called " The Bressler Report " by Jerome Bressler; and

>>

>>

>>

>> WHEREAS, in 1980, Dr. John Olney submitted scientific data to a United

>>States Food and Drug Administration Public Board of Inquiry showing that

>>aspartic acid, the excitotoxic ingredient in aspartame, caused holes in the

>>brains of mice; and

>>

>>

>>

>> WHEREAS, Dr. John Olney stated that it warranted special emphasis that

>>excitotoxins act by an acute but silent mechanism requiring only a single

>>exposure to toxic concentrations for CVO neurons to be quietly destroyed,

>>that clearly Searle failed to establish the safety of their product,

>>aspartame, for use in children's food, and that all age comparative data

>>support the following conclusions: (1) orally administered excitotoxins

>>destroy CVO neurons at any age; (2) immature animals are most vulnerable;

>>and (3) the toxic threshold increases only gradually between birth and

>>adulthood; and

>>

>>

>>

>> WHEREAS, in 1980, the Public Board of Inquiry unanimously voted against

>>aspartame approval, but was overruled by a new United States Food and Drug

>>Administration Commissioner, Dr. Arthur Hull Hays, against the advice of

>>Food and Drug Administration scientific personnel and advisers; and

>>

>>

>>

>> WHEREAS, the United States Food and Drug Administration approved

>>aspartame use in sodas, despite the fact that the National Soft Drink

>>Association argued vehemently against aspartame in these quotes from their

>>protest:

>>

>>

>>

>> (1) " The present record does not contain data which demonstrate that

>>the use of APM in soft drinks will not result in the adulteration of the

>>beverages under section 402(a)(3) of the FDC Act 21 U.S.C. 342(a)(3), which

>>provides that a food is adulterated if it contains, in whole or in part, " a

>>decomposed substance or if it is otherwise unfit for food " ;

>>

>>

>>

>> (2) " An important decomposition product of aspartame, aspartic acid,

>>cannot be detected at all using TLC " ;

>>

>>

>>

>> (3) " G. D. Searle and Company has not demonstrated to a reasonable

>>certainty that the use of aspartame in soft drinks, without quantitative

>>limitations, will not adversely affect human health as a result of the

>>changes such use is likely to cause in brain chemistry and under certain

>>reasonably anticipated conditions of use " ; and

>>

>>

>>

>> (4) " Specifically, Searle has not met its burdens under section

>>409....to demonstrate that aspartame is safe and functional for use in soft

>>drinks. Collectively, the extensive deficiencies in the stability studies

>>conducted by Searle to demonstrate that aspartame and its degradation

>>products are safe in soft drinks intended to be sold in the United States,

>>render those studies inadequate and unreliable. " Senate Congressional

>>Record, May 7, 1985, S5507–5511; and

>>

>>

>>

>> WHEREAS, the United States Food and Drug Administration has compiled a

>>list of ninety-two symptoms attributed to aspartame consumption including

>>four types of seizures, coma, and death; and

>>

>>

>>

>> WHEREAS, the Ramazzini Studies by the European Foundation for Oncology

>>in Italy conducted exhaustive studies over three years with thousands of

>>rats, and proved aspartame to be a multipotential carcinogen, thus

>>confirming the United States Food and Drug Administration's original

>>findings; and

>>

>>

>>

>> WHEREAS, the United States Food and Drug Administration admitted that

>>aspartame caused cancer over two decades ago when the Administration's

>>toxicologist, Dr. Adrian Gross, told Congress at least one of Searle's

>>studies " has established beyond any reasonable doubt that aspartame is

>>capable of inducing brain tumors in experimental animals and that this

>>predisposition of it is of extremely high significance....In view of these

>>indications that the cancer causing potential of aspartame is a matter that

>>had been established way beyond any reasonable doubt, one can ask: What is

>>the reason for the apparent refusal by the FDA to invoke for this food

>>additive the so-called Delaney Amendment to the Food, Drug and Cosmetic Act?

>>Given the cancer causing potential of aspartame how would the FDA justify

>>its position that it views a certain amount of aspartame as constituting an

>>allowable daily intake or 'safe' level of it? Is that position in effect not

>>equivalent to setting a 'tolerance' for this food additive and thus a

>>violation of that law? And if the FDA itself elects to violate the law, who

>>is left to protect the health of the public? " Congressional Record, August

>>1, l985, SID835:131; and

>>

>>

>>

>> WHEREAS, aspartame is linked to sudden death, multiple sclerosis,

>>lupus, and many neurodegenerative diseases, as cited in many medical texts,

>>most notably: Aspartame Disease: An Ignored Epidemic, by H.J. Roberts,

>>M.D., and Excitotoxins: The Taste That Kills, by Russell Blaylock, M.D.; and

>>

>>

>>

>> WHEREAS, on November 3, 1987, Dr. Louis Elsas told Congress: " I am a

>>pediatrician, a Professor of Pediatrics at Emory and have spent twenty-five

>>years in the biomedical sciences, trying to prevent mental retardation and

>>birth defect caused by excess phenylalanine, and therein lies my basic

>>concern, that aspartame is in fact a well known neurotoxin and teratogen

>>which, in some as yet undefined dose, will. . . irreversibly in the

>>developing child or fetal brain, produce adverse effects " ; and

>>

>>

>>

>> WHEREAS, there are tens of thousands of case histories and anecdotal

>>accounts from victims of aspartame poisoning who have come forward to make

>>their case histories known; now, therefore,

>>

>>

>>

>> BE IT RESOLVED that the Department of

>> Health is requested to create, within

>>their existing budget, an evidentiary repository accessible to the public

>>for patients and physicians to submit over the next year their cases

>>involving victims of aspartame poisoning; and

>>

>>

>> BE IT FURTHER RESOLVED that the Department of Health is requested to

>>review all existing reports, studies, experiments, and related literature on

>>aspartame, including clinical studies, differentiating each study by its

>>funding source, and submit a report; and

>>

>>

>>

>> BE IT FURTHER RESOLVED that the Ministry

>> of Health in this respective country

>> is requested to review all existing reports,

>> studies, experiments, and related

>>literature on aspartame, including clinical studies, differentiating each

>>study by its funding source, and that, if funding is required to undertake

>>this extended evaluation, that the appropriate funding be sought from

>>various foundations and from government; and

>>

>>

>>

>> BE IT FURTHER RESOLVED that given the enormous amount of evidence that

>>has been compiled concerning the neurodegenerative harm it can cause, that

>>the respective Ministry of Health is requested to rescind

>>approval of aspartame immediately on a phase-out basis over six months

>>to one year in the respective market.

>>This Resolution was written by Dr Betty Martini

>>of Mission Possible and Stephen Fox.

>>

>>Mission Possible (MP) is an international

>>organization with global chapters, headquartered in Duluth,, Georgia;

>>

>>MP was founded and is managed by Dr Martini who

>>has over 15 years experience on the subject of aspartame.

>>

>>For more information on aspartame and Mission

>>Possible:

>><http://www.dorway.com/possible.html>http://www.dorway.com/possible.html

>>

>>The International Resolution to Phase-out and Ban Aspartame globally

>>due to known and proven excitoneurotoxic and carcinogenic effects is an

>>initiative of, and distributed by, Mission

>>Possible and the Phoenix Environmental Institute (PEI).

>>

>>

>>Début du message réexpédié :

>>

>>>De : Corinne GOUGET

>>><<missionpossible.francemissionpossible.france

>>>Date : 19 septembre 2008 13:20:20 HAEC

>>>

>>>-----------\

--\

--\

--

>>>

>>>RESOLUTION INTERNATIONALE

>>>demandant aux autorités sanitaires de revoir

>>>tous les rapports et les études concernant

>>>l’aspartame et demandant au ministère de la

>>>santé du pays concerné d’annuler les

>>>autorisations de l’aspartame au public dans

>>>tous les domaines de vente de ce pays.

>>>

>>>SACHANT QUE l’aspartame fut développé à

>>>l’origine (en 1965) comme un médicament pour

>>>traiter les ulcères d’estomac et

>>>

>>>SACHANT QUE les fabricants déclarent que

>>>l’aspartame est composé à 40% d’acide

>>>aspartique, à 50 % de phénylalanine et à 10% de méthanol et

>>>

>>>SACHANT QUE l’acide aspartique est un acide

>>>aminé non essentiel utilisé par l’organisme

>>>pour provoquer l’apoptose ou la mort des cellules âgées et que

>>>l’excès d’acide aspartique lié à la

>>>consommation d’aspartame cause l’apoptose des

>>>cellules saines pouvant conduire à la destruction de tissus sains, tout

>>>particulièrement dans le cerveau et

>>>

>>>SACHANT QUE la phénylalanine est un acide

>>>aminé essentiel que l’on trouve naturellement

>>>dans les protéines mais qui devient

>>>neurotoxique sous sa forme pure, en abaissant le

>>>seuil de sensibilité aux attaques et en

>>>réduisant le taux de sérotonine, ce qui

>>>provoque des troubles psychiatriques et des

>>>problèmes comportementaux et qui interagit avec les

>>>antidépresseurs et les autres médicaments et

>>>

>>>SACHANT QUE le méthanol est un poison

>>>dangereux classé comme narcotique qui se

>>>convertit en formaldéhyde et en acide

>>>formique, provoquant le dessèchement des tissus

>>>vivants et endommageant l’ADN et

>>>

>>>SACHANT QUE parmi les métabolites de

>>>l’aspartame, on trouve le formaldéhyde, agent

>>>cancérigène de classe “A”, la dicétopipérazine, agent provoquant des tumeurs

>>>cérébrales ainsi que l’acide formique et

>>>

>>>SACHANT QU’ en 1974 la FDA américaine avait

>>>autorisé l’aspartame en tant qu’édulcorant de

>>>synthèse mais avait demandé à son fabricant SEARLE, d’en retarder la

>>>mise sur le marché en attendant que des tests

>>>supplémentaires soient réalisés concernant son innocuité et

>>>

>>>SACHANT QUE les données scientifiques ayant

>>>révélé un problème au niveau des données de

>>>sûreté et cela a conduit la FDA américaine à retirer son autorisation et

>>>

>>>SACHANT QU' en 1975, la FDA qui avait ordonné

>>>une enquête au sujet des pratiques des

>>>laboratoires SEARLE, avait découvert des fraudes lors d’expériences

>>>scientifiques ainsi que des données trafiquées

>>>tendant à faire croire que l’aspartame était sans dangers et

>>>

>>>SACHANT QU’ en 1977, les résultats de cette

>>>enquête ont été inclus dans ce que l’on

>>>appelle “The BRESSLER REPORT” de Jérôme Bressler et

>>>

>>>SACHANT QU' en 1980 le Dr John OLNEY ayant

>>>présenté des données scientifiques dans le

>>>cadre d’une enquête d’utilité publique commanditée par la FDA américaine,

>>>prouvant que l’acide aspartique; excitotoxine

>>>présente dans l’aspartame, causait des trous dans le cerveau de souris et

>>>

>>>SACHANT QUE le Dr John Olney ajoutait qu’il

>>>fallait insister tout particulièrement sur le

>>>fait que les excitotoxines agissaient de

>>>manière aiguë mais par un mécanisme silencieux

>>>nécessitant un seule exposition pour atteindre

>>>une concentration toxique pour que les

>>>neurones des organes circumventriculaires

>>>(OCV) soient discrètement détruits, et que

>>>SEARLE n’avait pas réussi à établir de manière

>>>claire l’innocuité de leur produit,

>>>l’aspartame, comme additif dans les aliments

>>>pour enfants, et que les données comparatives

>>>concernant toutes les tranches d’âges soutenaient les conclusions suivantes:

>>>

>>>- Les excitotoxines administrées par voie

>>>orale peuvent détruire les neurones des OCV à tout âge.

>>>

>>>- Les animaux immatures sont les plus vulnérables

>>>

>>>- Le niveau de toxicité n’augmente que

>>>graduellement entre la naissance et l’âge adulte .

>>>

>>>SACHANT QU' aux USA, en 1980, la commission

>>>d’enquête d’utilité publique avait voté à

>>>l’unanimité contre l’autorisation de l’aspartame, mais que ce vote avait

>>>été rejeté par le nouveau responsable de la

>>>FDA américaine, le Dr Arthur Hull HAYES contre

>>>l’avis du personnel scientifique et des conseillers de la FDA et

>>>

>>>SACHANT QUE la FDA américaine a autorisé

>>>l’utilisation de l’aspartame dans les sodas,

>>>malgré le fait que la National Soft Drink Association,2422 se soit vivement

>>>opposée à son utilisation comme en témoigne un extrait de leur rapport:

>>>

>>>(1)“Les données actuelles ne comportent aucune

>>>preuve garantissant que l’utilisation de

>>>l’aspartame dans les sodas ne provoquera pas une altération des boissons

comme

>>>prévu par la loi 402(a)(3) du FDC Act 21

>>>U.S.C.342(a)(3), qui prévoit qu’un aliment est

>>>altéré s’il contient en partie ou dans sa totalité “une substance décomposée

ou

>>>s’il devient tout simplement non comestible”.

>>>

>>>“L’aspartame est constitué en majorité d’acide

>>>aspartique, un produit qu’il est impossible de

>>>détecter par chromatographie en couches minces (TLC)”

>>>

>>>“G.D.Searle et Cie n’a pu prouver de manière

>>>suffisamment certaine que l’utilisation sans

>>>limite quantitative de l’aspartame dans les

>>>sodas n’aurait pas d’effets néfastes pour la

>>>santé humaine, en raison des possibles

>>>modifications de la chimie du cerveau liées à

>>>un emploi en excès facilement prévisible” et

>>>

>>>“En particulier, Searle n’a pas rempli ses

>>>devoirs selon l’article 409... en démontrant

>>>que l’aspartame était un produit sans

>>>dangers et fonctionnel pour les sodas. En

>>>résumé, les nombreuses déficiences concernant

>>>les études de stabilité de l’aspartame menées

>>>par Searle pour démontrer que l’aspartame et

>>>ses produits de dégradation, sont sans

>>>dangers pour des sodas destinés à la vente

>>>aux USA, rendent ces études non pertinentes et

>>>non fiables” (Senate Congressional Record, May 7, 1985,S5507-5511 et

>>>

>>>SACHANT QUE depuis le 20/04/95, la FDA

>>>américaine a dressé une liste de 92 effets

>>>secondaires liés à la consommation d’aspartame

>>>dont quatre cas d’attaques cérébrales

>>>de coma et de mort et

>>>

>>>SACHANT QUE les études approfondies menées sur

>>>des milliers de rats en Italie par l’Institut

>>>de Ramazzini pour le compte de la Fondation Européenne d’Oncologie sur

>>>une durée de trois années, ont prouvé que

>>>l’aspartame était un carcinogène à

>>>potentialités multiples, confirmant ainsi les

>>>premières découvertes de la FDA américaine et

>>>

>>>SACHANT QU’ il y a 20 ans, la FDA américaine

>>>avait admis que l’aspartame pouvait provoquer

>>>des cancers suite aux déclarations devant le

>>>Congrès de leur propre toxicologue; le Dr

>>>Adrian Gross, selon lesquelles au moins une

>>>des études de Searle “avait établi sans aucun

>>>doute possible que l’aspartame était capable

>>>d’induire des tumeurs cérébrales chez des

>>>animaux de laboratoire et que cette

>>>prédisposition au cancer était extrêmement

>>>significative... Au vu de ces indices forts et

>>>convergents concernant le risque carcinogène

>>>potentiel de l’aspartame, on peut se demander :

>>>

>>>- Quelle est la raison du refus apparent de la

>>>FDA d’évoquer au sujet de cet additif

>>>alimentaire l’amendement dit “Delaney” à la

>>>loi sur les aliments, les médicaments et les cosmétiques?

>>>- Connaissant le potentiel carcinogène de

>>>l’aspartame, comment la FDA , pourrait-elle

>>>justifier sa position selon laquelle une certaine dose quotidienne

d’aspartame,

>>>pouvait constituer une dose journalière

>>>acceptable et sans dangers? Cette position

>>>n’est elle pas équivalente dans ses effets à

>>>fixer un seuil de “tolérance” pour cet

>>>additif alimentaire, entraînant une violation

>>>de la loi? Et si la FDA décide elle même de

>>>violer la loi, qui d’autre sera en mesure de

>>>protéger la santé publique ?” Registre

>>>du Congrès, 1er août 1985, SID835:131; (Il en

>>>est de même pour l'EFSA (Autorité européenne

>>>de sécurité des aliments) et l' AFSSA (Agence française de sécurité sanitaire

>>>des aliments) en France) et

>>>

>>>SACHANT QUE l’aspartame est en rapport avec

>>>des cas de morts subites, de scléroses en

>>>plaque, de lupus et de nombreuses autres maladies neurodégénératives comme en

>>>témoignent de nombreux textes scientifiques,

>>>notamment : “Aspartame Disease : An Ignored

>>>Epidemic” de H.J. Roberts M.D. et

>>>“Excitotoxins:The Taste That Kills” de Russell Blaylock, M.D. et

>>>

>>>SACHANT QUE le 3 novembre 1987, le Dr Louis

>>>Elsa a déclaré devant le Congrès: “Je suis

>>>pédiatre, professeur en pédiatrie à Emory et

>>>j’ai passé 25 ans à étudier les sciences

>>>biomédicales, en essayant de prévenir les

>>>retards mentaux et les déformations

>>>congénitales provoqués par un excès de

>>>phénylalanine, expliquant mon souci principal

>>>d’informer que l’aspartame est de manière

>>>notoire une neurotoxine et un agent tératogène

>>>et ceci à toutes doses, .... pouvant provoquer

>>>de manière irréversible des effets nuisibles

>>>chez l’enfant en pleine croissance ou le cerveau du foetus” .

>>>

>>>SACHANT QU’ il existe des dizaines de milliers

>>>de cas et d’anecdotes rapportés par des

>>>victimes de l’empoisonnement à l’aspartame et

>>>ayant tenu à rendre publique leur expérience; il est temps dorénavant,

>>>

>>>D’EXIGER de la part du Ministère de la Santé

>>>de créer dans les limites du budget existant,

>>>une archive de témoignages accessible au

>>>public, aux patients ainsi qu’aux médecins

>>>afin que les nombreux cas de victimes

>>>d’empoisonnement à l’aspartame pour l’année à venir soient rendus publics et

>>>

>>>D’EXIGER AUSSI que le Ministère de la Santé

>>>procède à une revue exhaustive de tous les

>>>rapports, études, expériences et ouvrages concernant l’aspartame, y compris

>>>les études cliniques en identifiant à chaque

>>>fois les sources de financement, en vue de soumettre un rapport et

>>>

>>>D’EXIGER AUSSI que le Ministère de la Santé

>>>procède à une revue exhaustive de tous les

>>>rapports, études, expériences et ouvrages concernant l’aspartame, y compris

>>>les études cliniques en identifiant à chaque

>>>fois les sources de financement, et qu’en cas

>>>d’évaluation supplémentaire requise, que les

>>>fonds nécessaires soient réclamés auprès des

>>>différentes fondations ainsi qu’auprès du gouvernement et

>>>

>>>D’EXIGER AUSSI, que compte tenu des très

>>>nombreuses preuves accumulées concernant les

>>>dégâts neurologiques que l’aspartame peut causer, que le Ministère de la

>>>Santé concerné annule l’autorisation d’emploi

>>>de l’aspartame et que soit mise en place

>>>immédiatement son retrait progressif du marché

>>>dans un délai de six à douze mois selon les marchés concernés.

>>>

>>>Cette Résolution a été écrite par le Dr Betty

>>>Martini, présidente de l’association Mission

>>>Possible International et par Stephen Fox.

>>>Mission Possible (MP) est une organisation

>>>internationale dont le siège est à Atlanta (Géorgie, USA).

>>>

>>>MP a été créée et dirigée par le Dr Betty

>>>Martini qui a une expérience de plus de 15 ans dans le domaine de

l’aspartame:

>>>

>>>Dr. Betty Martini, D.Hum, Founder

>>>

>>>Mission Possible International

>>>9270 River Club Parkway

>>>Duluth, Georgia 30097

>>>770 242-2599

>>>USA

>>>

>>>

>>><http://www.mpwhi.com/>www.mpwhi.com,

>>>www.dorway.com and www.wnho.net Aspartame

>>>Toxicity Center, <http://www.holisticmed.com/>www.holisticmed.com/

>>>

>>>Email: <bettym19bettym19

>>>

>>>

>>>Pour plus d’informations sur l’aspartame et sur Mission Possible:

>>>

>>><http://www.dorway.com/possible.html>http://www.dorway.com/possible.html

>>>

>>>

>>>Cette Résolution Internationale pour

>>>l’élimination et l’interdiction de l’aspartame

>>>dans le monde en raison des preuves reconnues

>>>de son excito-neurotoxicité et de ses

>>>effets cancérigènes, est distribuée par

>>>Mission Possible et par l’Institut Environnemental Phoenix (PEI)

>>>

>>>

>>>

>>>

>>>

>>>

>>>

>>>

>>>-----------\

--\

--\

------

>>>

>>>

>>>

>>>

>>>Le 19 août 08 à 11:53, Khadija Sharife a écrit :

>>>

>>>>----------\

-------

>>>>>Please remember that aspartame is an

>>>>>excitotoxin and that children are far more

>>>>>sensitives to this POISON than adults... And

>>>>>please consider the followng references:

>>>>>

>>>>><http://www.mpwhi.com/report_on_aspartame_and_children.htm>http://www.mpwhi\

..com/report_on_aspartame_and_children.htm

>>>>>

>>>>>http://www.dorway.com/

>>>>>

>>>>>

>>>>>

>>>>>

>>>>> TOGETHER WE COULD MAKE A DIFFERENCE FOR THE GENERATIONS TO COME!

>>>>>

>>>>>Corinne GOUGET

>>>>>

>>>>Le 12 août 08 à 11:30, Khadija Sharife a écrit :

>>>>

>>>>>

>>>>>

>>>>>RESOLUTION

>>>>>

>>>>>

>>>>>REQUESTING THE DEPARTMENT OF HEALTH TO REVIEW EXISTING REPORTS

>>>>>AND STUDIES RELATED TO ASPARTAME, AND REQUESTING THE MINISTRY OF

>>>>>HEALTH IN THIS RESPECTIVE COUNTRY TO RESCIND APPROVAL OF ASPARTAME

>>>>>FOR SALE TO THE PUBLIC IN THE MARKETS OF THIS COUNTRY.

>>>>>

>>>>>

>>>>> WHEREAS, aspartame was originally developed as a drug to treat peptic

>>>>>ulcers; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, manufacturers state that aspartame is made up of forty per

>>>>>cent aspartic acid, fifty per cent

>>>>>phenylalanine, and ten per cent methanol;

>>>>>and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, aspartic acid is a

>>>>> nonessential amino acid that is used by the

>>>>>body to initiate apoptosis or cell death in aging cells, and that excess

>>>>>aspartic acid from aspartame consumption causes apoptosis in healthy cells

>>>>>that can destroy healthy tissue, especially in the brain; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, phenylalanine is an essential amino acid found naturally in

>>>>>protein but when isolated becomes

>>>>>neurotoxic, lowers the seizure threshold,

>>>>>depletes serotonin triggering psychiatric and behavioral problems, and

>>>>>interacts with antidepressants and other drugs; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, methanol is a severe metabolic

>>>>> poison classified as a narcotic

>>>>>that converts to formaldehyde and formic

>>>>>acid, and can embalm living tissue

>>>>>and damage DNA; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, aspartame metabolites include formaldehyde, a " class A "

>>>>>carcinogen, diketopiperazine, a brain tumor agent, and formic acid; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, in 1974, the United States Food and Drug Administration

>>>>>approved aspartame as an artificial sweetener, but asked its manufacturer

>>>>>Searle to hold back from selling it on the

>>>>>market until further tests could

>>>>>be made with regards to its safety; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, scientific data revealed that there was a problem with

>>>>>aspartame safety data and the United States Food and Drug Administration

>>>>>withdrew its approval; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, in 1975, the United States Food and Drug Administration

>>>>>initiated an investigation into Searle's

>>>>>laboratory practices and discovered

>>>>>fraud in scientific experiments as well as

>>>>>manipulated data giving favorable

>>>>>results proving aspartame to be safe; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, the results of this investigation are included in what is

>>>>>called " The Bressler Report " by Jerome Bressler; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, in 1980, Dr. John Olney

>>>>> submitted scientific data to a United

>>>>>States Food and Drug Administration Public Board of Inquiry showing that

>>>>>aspartic acid, the excitotoxic ingredient in

>>>>>aspartame, caused holes in the

>>>>>brains of mice; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, Dr. John Olney stated that it

>>>>> warranted special emphasis that

>>>>>excitotoxins act by an acute but silent mechanism requiring only a single

>>>>>exposure to toxic concentrations for CVO neurons to be quietly destroyed,

>>>>>that clearly Searle failed to establish the safety of their product,

>>>>>aspartame, for use in children's food, and that all age comparative data

>>>>>support the following conclusions: (1) orally administered excitotoxins

>>>>>destroy CVO neurons at any age; (2) immature animals are most vulnerable;

>>>>>and (3) the toxic threshold increases only gradually between birth and

>>>>>adulthood; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, in 1980, the Public Board of

>>>>> Inquiry unanimously voted against

>>>>>aspartame approval, but was overruled by a new United States Food and Drug

>>>>>Administration Commissioner, Dr. Arthur Hull Hays, against the advice of

>>>>>Food and Drug Administration scientific personnel and advisers; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, the United States Food and Drug Administration approved

>>>>>aspartame use in sodas, despite the fact that the National Soft Drink

>>>>>Association argued vehemently against aspartame in these quotes from their

>>>>>protest:

>>>>>

>>>>>

>>>>>

>>>>> (1) " The present record does not contain data which demonstrate that

>>>>>the use of APM in soft drinks will not result in the adulteration of the

>>>>>beverages under section 402(a)(3) of the FDC

>>>>>Act 21 U.S.C. 342(a)(3), which

>>>>>provides that a food is adulterated if it

>>>>>contains, in whole or in part, " a

>>>>>decomposed substance or if it is otherwise unfit for food " ;

>>>>>

>>>>>

>>>>>

>>>>> (2) " An important decomposition product of aspartame, aspartic acid,

>>>>>cannot be detected at all using TLC " ;

>>>>>

>>>>>

>>>>>

>>>>> (3) " G. D. Searle and Company has not demonstrated to a reasonable

>>>>>certainty that the use of aspartame in soft drinks, without quantitative

>>>>>limitations, will not adversely affect human health as a result of the

>>>>>changes such use is likely to cause in brain chemistry and under certain

>>>>>reasonably anticipated conditions of use " ; and

>>>>>

>>>>>

>>>>>

>>>>> (4) " Specifically, Searle has not met its burdens under section

>>>>>409....to demonstrate that aspartame is safe

>>>>>and functional for use in soft

>>>>>drinks. Collectively, the extensive deficiencies in the stability studies

>>>>>conducted by Searle to demonstrate that aspartame and its degradation

>>>>>products are safe in soft drinks intended to be sold in the United States,

>>>>>render those studies inadequate and unreliable. " Senate Congressional

>>>>>Record, May 7, 1985, S5507–5511; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, the United States Food and

>>>>> Drug Administration has compiled a

>>>>>list of ninety-two symptoms attributed to aspartame consumption including

>>>>>four types of seizures, coma, and death; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, the Ramazzini Studies by the

>>>>> European Foundation for Oncology

>>>>>in Italy conducted exhaustive studies over three years with thousands of

>>>>>rats, and proved aspartame to be a multipotential carcinogen, thus

>>>>>confirming the United States Food and Drug Administration's original

>>>>>findings; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, the United States Food and Drug Administration admitted that

>>>>>aspartame caused cancer over two decades ago when the Administration's

>>>>>toxicologist, Dr. Adrian Gross, told Congress at least one of Searle's

>>>>>studies " has established beyond any reasonable doubt that aspartame is

>>>>>capable of inducing brain tumors in experimental animals and that this

>>>>>predisposition of it is of extremely high significance....In view of these

>>>>>indications that the cancer causing

>>>>>potential of aspartame is a matter that

>>>>>had been established way beyond any reasonable doubt, one can ask: What is

>>>>>the reason for the apparent refusal by the FDA to invoke for this food

>>>>>additive the so-called Delaney Amendment to

>>>>>the Food, Drug and Cosmetic Act?

>>>>>Given the cancer causing potential of aspartame how would the FDA justify

>>>>>its position that it views a certain amount

>>>>>of aspartame as constituting an

>>>>>allowable daily intake or 'safe' level of

>>>>>it? Is that position in effect not

>>>>>equivalent to setting a 'tolerance' for this food additive and thus a

>>>>>violation of that law? And if the FDA

>>>>>itself elects to violate the law, who

>>>>>is left to protect the health of the public? " Congressional Record, August

>>>>>1, l985, SID835:131; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, aspartame is linked to sudden death, multiple sclerosis,

>>>>>lupus, and many neurodegenerative diseases,

>>>>>as cited in many medical texts,

>>>>>most notably: Aspartame Disease: An Ignored Epidemic, by H.J. Roberts,

>>>>>M.D., and Excitotoxins: The Taste That

>>>>>Kills, by Russell Blaylock, M.D.; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, on November 3, 1987, Dr. Louis Elsas told Congress: " I am a

>>>>>pediatrician, a Professor of Pediatrics at

>>>>>Emory and have spent twenty-five

>>>>>years in the biomedical sciences, trying to prevent mental retardation and

>>>>>birth defect caused by excess phenylalanine, and therein lies my basic

>>>>>concern, that aspartame is in fact a well known neurotoxin and teratogen

>>>>>which, in some as yet undefined dose, will. . . irreversibly in the

>>>>>developing child or fetal brain, produce adverse effects " ; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, there are tens of thousands of case histories and anecdotal

>>>>>accounts from victims of aspartame poisoning who have come forward to make

>>>>>their case histories known; now, therefore,

>>>>>

>>>>>

>>>>>

>>>>> BE IT RESOLVED that the Department of

>>>>> Health is requested to create, within

>>>>>their existing budget, an evidentiary repository accessible to the public

>>>>>for patients and physicians to submit over the next year their cases

>>>>>involving victims of aspartame poisoning; and

>>>>>

>>>>>

>>>>> BE IT FURTHER RESOLVED that the Department of Health is requested to

>>>>>review all existing reports, studies,

>>>>>experiments, and related literature on

>>>>>aspartame, including clinical studies, differentiating each study by its

>>>>>funding source, and submit a report; and

>>>>>

>>>>>

>>>>>

>>>>> BE IT FURTHER RESOLVED that the

>>>>> Ministry of Health in this respective country

>>>>> is requested to review all existing

>>>>> reports, studies, experiments, and related

>>>>>literature on aspartame, including clinical studies, differentiating each

>>>>>study by its funding source, and that, if funding is required to undertake

>>>>>this extended evaluation, that the appropriate funding be sought from

>>>>>various foundations and from government; and

>>>>>

>>>>>

>>>>>

>>>>> BE IT FURTHER RESOLVED that given the enormous amount of evidence that

>>>>>has been compiled concerning the neurodegenerative harm it can cause, that

>>>>>the respective Ministry of Health is requested to rescind

>>>>>approval of aspartame immediately on a phase-out basis over six months

>>>>>to one year in the respective market.

>>>>>

>>>>>This Resolution was written by Dr Betty

>>>>>Martini of Mission Possible and Stephen Fox.

>>>>>

>>>>>Mission Possible (MP) is an international

>>>>>organization with global chapters, headquartered in Atlanta, Georgia;

>>>>>

>>>>>MP was founded and is managed by Dr Martini

>>>>>who has over 15 years experience on the subject of aspartame.

>>>>>

>>>>>For more information on aspartame and

>>>>>Mission Possible:

>>>>><http://www.dorway.com/possible.html>http://www.dorway.com/possible.html

>>>>>

>>>>>The International Resolution to Phase-out and Ban Aspartame globally

>>>>>due to known and proven excitoneurotoxic and carcinogenic effects is an

>>>>>initiative of, and distributed by, Mission

>>>>>Possible and the Phoenix Environmental Institute (PEI).

>>>>>

>>>>>

>>>>>On Sun, Aug 10, 2008 at 10:25 PM, corinne

>>>>>gouget <<lavieausoleil16lavieausoleil16 wrote:

>>>>>Dear Khadija,

>>>>>

>>>>>yes I am Mission Possible France and I would

>>>>>be happy to translate your resolution, could

>>>>>you tell me how long it is when you need it for.

>>>>>

>>>>>Here in France aspartame is destroying

>>>>>milions of lives..... I met over thousand 's

>>>>>of aspartame vicitms in this country and the

>>>>>children cases are deeply painful... I wrote

>>>>>a book in fench about food additives and it is a best seller! Do you know

it ?

>>>>>It is small and orange and I do have over 61,000 readers aged 6 to 90!

>>>>> " ADDITIFS ALIMENTAIRES DANGER " Editions du Chariot d'Or.

>>>>>

>>>>>But because of my book and conferences

>>>>>regarding aspartame and MSG all over the

>>>>>country, I sudenly lost custody of my two

>>>>>young daugthers over two years ago and I do

>>>>>miss them a lot. Today I had to move four

>>>>>times and I am due to meet my 15th lawyer

>>>>>next week to see if he could help me to see

>>>>>my children again and to get them back. I

>>>>>should write another book about how

>>>>>aspartame destroyed my family and my children infancy. Once I

>>>>>

>>>>><missionpossible.franceWell

>>>>>I will ask you to reply to me using the following address:

>>>>>

>>>>>Thank you and all the best in South Africa,

>>>>>

>>>>>Corinne GOUGET

>>>>>

>>>>>----- Message d'origine ----

>>>>>De : Khadija Sharife <<kalebronkalebron

>>>>>À : <lavieausoleil16lavieausoleil16

>>>>>Envoyé le : Dimanche, 10 Août 2008, 12h49mn 56s

>>>>>Objet : from Dr Betty Martini contact in South Africa

>>>>>

>>>>>

>>>>>

>>>>>

>>>>>

>>>>>

>>>>>

>>>>>

>>>>>RESOLUTION

>>>>>

>>>>>

>>>>>REQUESTING THE DEPARTMENT OF HEALTH TO REVIEW EXISTING REPORTS

>>>>>AND STUDIES RELATED TO ASPARTAME, AND REQUESTING THE MINISTRY OF

>>>>>HEALTH IN THIS RESPECTIVE COUNTRY TO RESCIND APPROVAL OF ASPARTAME

>>>>>FOR SALE TO THE PUBLIC IN THE MARKETS OF THIS COUNTRY.

>>>>>

>>>>>

>>>>> WHEREAS, aspartame was originally developed as a drug to treat peptic

>>>>>ulcers; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, manufacturers state that aspartame is made up of forty per

>>>>>cent aspartic acid, fifty per cent

>>>>>phenylalanine, and ten per cent methanol;

>>>>>and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, aspartic acid is a

>>>>> nonessential amino acid that is used by the

>>>>>body to initiate apoptosis or cell death in aging cells, and that excess

>>>>>aspartic acid from aspartame consumption causes apoptosis in healthy cells

>>>>>that can destroy healthy tissue, especially in the brain; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, phenylalanine is an essential amino acid found naturally in

>>>>>protein but when isolated becomes

>>>>>neurotoxic, lowers the seizure threshold,

>>>>>depletes serotonin triggering psychiatric and behavioral problems, and

>>>>>interacts with antidepressants and other drugs; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, methanol is a severe metabolic

>>>>> poison classified as a narcotic

>>>>>that converts to formaldehyde and formic

>>>>>acid, and can embalm living tissue

>>>>>and damage DNA; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, aspartame metabolites include formaldehyde, a " class A "

>>>>>carcinogen, diketopiperazine, a brain tumor agent, and formic acid; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, in 1974, the United States Food and Drug Administration

>>>>>approved aspartame as an artificial sweetener, but asked its manufacturer

>>>>>Searle to hold back from selling it on the

>>>>>market until further tests could

>>>>>be made with regards to its safety; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, scientific data revealed that there was a problem with

>>>>>aspartame safety data and the United States Food and Drug Administration

>>>>>withdrew its approval; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, in 1975, the United States Food and Drug Administration

>>>>>initiated an investigation into Searle's

>>>>>laboratory practices and discovered

>>>>>fraud in scientific experiments as well as

>>>>>manipulated data giving favorable

>>>>>results proving aspartame to be safe; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, the results of this investigation are included in what is

>>>>>called " The Bressler Report " by Jerome Bressler; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, in 1980, Dr. John Olney

>>>>> submitted scientific data to a United

>>>>>States Food and Drug Administration Public Board of Inquiry showing that

>>>>>aspartic acid, the excitotoxic ingredient in

>>>>>aspartame, caused holes in the

>>>>>brains of mice; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, Dr. John Olney stated that it

>>>>> warranted special emphasis that

>>>>>excitotoxins act by an acute but silent mechanism requiring only a single

>>>>>exposure to toxic concentrations for CVO neurons to be quietly destroyed,

>>>>>that clearly Searle failed to establish the safety of their product,

>>>>>aspartame, for use in children's food, and that all age comparative data

>>>>>support the following conclusions: (1) orally administered excitotoxins

>>>>>destroy CVO neurons at any age; (2) immature animals are most vulnerable;

>>>>>and (3) the toxic threshold increases only gradually between birth and

>>>>>adulthood; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, in 1980, the Public Board of

>>>>> Inquiry unanimously voted against

>>>>>aspartame approval, but was overruled by a new United States Food and Drug

>>>>>Administration Commissioner, Dr. Arthur Hull Hays, against the advice of

>>>>>Food and Drug Administration scientific personnel and advisers; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, the United States Food and Drug Administration approved

>>>>>aspartame use in sodas, despite the fact that the National Soft Drink

>>>>>Association argued vehemently against aspartame in these quotes from their

>>>>>protest:

>>>>>

>>>>>

>>>>>

>>>>> (1) " The present record does not contain data which demonstrate that

>>>>>the use of APM in soft drinks will not result in the adulteration of the

>>>>>beverages under section 402(a)(3) of the FDC

>>>>>Act 21 U.S.C. 342(a)(3), which

>>>>>provides that a food is adulterated if it

>>>>>contains, in whole or in part, " a

>>>>>decomposed substance or if it is otherwise unfit for food " ;

>>>>>

>>>>>

>>>>>

>>>>> (2) " An important decomposition product of aspartame, aspartic acid,

>>>>>cannot be detected at all using TLC " ;

>>>>>

>>>>>

>>>>>

>>>>> (3) " G. D. Searle and Company has not demonstrated to a reasonable

>>>>>certainty that the use of aspartame in soft drinks, without quantitative

>>>>>limitations, will not adversely affect human health as a result of the

>>>>>changes such use is likely to cause in brain chemistry and under certain

>>>>>reasonably anticipated conditions of use " ; and

>>>>>

>>>>>

>>>>>

>>>>> (4) " Specifically, Searle has not met its burdens under section

>>>>>409....to demonstrate that aspartame is safe

>>>>>and functional for use in soft

>>>>>drinks. Collectively, the extensive deficiencies in the stability studies

>>>>>conducted by Searle to demonstrate that aspartame and its degradation

>>>>>products are safe in soft drinks intended to be sold in the United States,

>>>>>render those studies inadequate and unreliable. " Senate Congressional

>>>>>Record, May 7, 1985, S5507–5511; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, the United States Food and

>>>>> Drug Administration has compiled a

>>>>>list of ninety-two symptoms attributed to aspartame consumption including

>>>>>four types of seizures, coma, and death; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, the Ramazzini Studies by the

>>>>> European Foundation for Oncology

>>>>>in Italy conducted exhaustive studies over three years with thousands of

>>>>>rats, and proved aspartame to be a multipotential carcinogen, thus

>>>>>confirming the United States Food and Drug Administration's original

>>>>>findings; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, the United States Food and Drug Administration admitted that

>>>>>aspartame caused cancer over two decades ago when the Administration's

>>>>>toxicologist, Dr. Adrian Gross, told Congress at least one of Searle's

>>>>>studies " has established beyond any reasonable doubt that aspartame is

>>>>>capable of inducing brain tumors in experimental animals and that this

>>>>>predisposition of it is of extremely high significance....In view of these

>>>>>indications that the cancer causing

>>>>>potential of aspartame is a matter that

>>>>>had been established way beyond any reasonable doubt, one can ask: What is

>>>>>the reason for the apparent refusal by the FDA to invoke for this food

>>>>>additive the so-called Delaney Amendment to

>>>>>the Food, Drug and Cosmetic Act?

>>>>>Given the cancer causing potential of aspartame how would the FDA justify

>>>>>its position that it views a certain amount

>>>>>of aspartame as constituting an

>>>>>allowable daily intake or 'safe' level of

>>>>>it? Is that position in effect not

>>>>>equivalent to setting a 'tolerance' for this food additive and thus a

>>>>>violation of that law? And if the FDA

>>>>>itself elects to violate the law, who

>>>>>is left to protect the health of the public? " Congressional Record, August

>>>>>1, l985, SID835:131; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, aspartame is linked to sudden death, multiple sclerosis,

>>>>>lupus, and many neurodegenerative diseases,

>>>>>as cited in many medical texts,

>>>>>most notably: Aspartame Disease: An Ignored Epidemic, by H.J. Roberts,

>>>>>M.D., and Excitotoxins: The Taste That

>>>>>Kills, by Russell Blaylock, M.D.; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, on November 3, 1987, Dr. Louis Elsas told Congress: " I am a

>>>>>pediatrician, a Professor of Pediatrics at

>>>>>Emory and have spent twenty-five

>>>>>years in the biomedical sciences, trying to prevent mental retardation and

>>>>>birth defect caused by excess phenylalanine, and therein lies my basic

>>>>>concern, that aspartame is in fact a well known neurotoxin and teratogen

>>>>>which, in some as yet undefined dose, will. . . irreversibly in the

>>>>>developing child or fetal brain, produce adverse effects " ; and

>>>>>

>>>>>

>>>>>

>>>>> WHEREAS, there are tens of thousands of case histories and anecdotal

>>>>>accounts from victims of aspartame poisoning who have come forward to make

>>>>>their case histories known; now, therefore,

>>>>>

>>>>>

>>>>>

>>>>> BE IT RESOLVED that the Department of

>>>>> Health is requested to create, within

>>>>>their existing budget, an evidentiary repository accessible to the public

>>>>>for patients and physicians to submit over the next year their cases

>>>>>involving victims of aspartame poisoning; and

>>>>>

>>>>>

>>>>> BE IT FURTHER RESOLVED that the Department of Health is requested to

>>>>>review all existing reports, studies,

>>>>>experiments, and related literature on

>>>>>aspartame, including clinical studies, differentiating each study by its

>>>>>funding source, and submit a report; and

>>>>>

>>>>>

>>>>>

>>>>> BE IT FURTHER RESOLVED that the

>>>>> Ministry of Health in this respective country

>>>>> is requested to review all existing

>>>>> reports, studies, experiments, and related

>>>>>literature on aspartame, including clinical studies, differentiating each

>>>>>study by its funding source, and that, if funding is required to undertake

>>>>>this extended evaluation, that the appropriate funding be sought from

>>>>>various foundations and from government; and

>>>>>

>>>>>

>>>>>

>>>>> BE IT FURTHER RESOLVED that given the enormous amount of evidence that

>>>>>has been compiled concerning the neurodegenerative harm it can cause, that

>>>>>the respective Ministry of Health is requested to rescind

>>>>>approval of aspartame immediately on a phase-out basis over six months

>>>>>to one year in the respective market.

>>>>>

>>>>>This Resolution was written by Dr Betty

>>>>>Martini of Mission Possible and Stephen Fox.

>>>>>

>>>>>Mission Possible (MP) is an international

>>>>>organization with global chapters, headquartered in Atlanta, Georgia;

>>>>>

>>>>>MP was founded and is managed by Dr Martini

>>>>>who has over 15 years experience on the subject of aspartame.

>>>>>For more information on aspartame and

>>>>>Mission Possible:

>>>>><http://www.dorway.com/possible.html>http://www.dorway.com/possible.html

>>>>>

>>>>>The International Resolution to Phase-out and Ban Aspartame globally

>>>>>due to known and proven excitoneurotoxic and carcinogenic effects is an

>>>>>initiative of, and distributed by, Mission

>>>>>Possible and the Phoenix Environmental Institute (PEI)

>>>>>

>>>>>

>>>>>

>>>>>

>>>>>Envoyé avec

>>>>><http://us.rd./mailuk/taglines/isp/control/*http://us.rd.\

/evt=52423/*http://fr.docs./mail/overview/index.html>!

>>>>>Mail.

>>>>>Une boite mail plus intelligente.

>>>>>

>>>>

>

>

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