Company Refuses To Pull
Aspartame From
Parkinson's Drug

From Dr. Betty Martini, D.Hum
It has been almost two weeks since I wrote you this letter. And I called before that. I just want to advise you if aspartame is not removed from Parcopa within two weeks, the information below will go out as a global press release. One victim just went through the agonizing withdrawal from the aspartame in the product. I do not want to see anyone go through what she did, sick taking the drug in the first place, and then the withdrawal process from the aspartame. Aspartame liberates free methyl alcohol. Methanol is classified as a narcotic. The chronic methanol poisoning affects the dopamine system of the brain and causes addiction.
This information as you see below is already posted to alert the public. I can't imagine a pharmaceutical company adding a neurotoxin to a drug and not even doing any research. Obviously with warnings on over 2 million web sites and medical books on it, it would be hard to not know. Then refusing to answer this is unconscionable.
Dr. Betty Martini, D. Hum., Founder,
Mission Possible International
9270 River Club Parkway
Duluth, Georgia 30097
770 242-2599 and
Aspartame Toxicity Center,
By Dr. Betty Martini
Mission Possible International
9270 River Club Parkway
Duluth, Georgia 30097
Telephone: 770-242-2599
Web Site: &
Date: Fri, 20 Jan 2006 20:28:05 -0500
From: "Dr. Betty Martini,D.Hum."
Subject: Remove aspartame from the Parkinson drug, Parcopa. It can precipitate the disease!
This is an urgent request for you to remove aspartame from Parcopa.
First of all, here are some points from neurosurgeon Russell Blaylock, M.D., author of Excitotoxins: The Taste That Kills:
* Parkinson's Disease is a disorder whose cause appears from substantial evidence to be related to excitotoxicity. These toxins destroy the cells in the brain central to this disease.
* Excitotoxins cause these brain cells to generate enormous amounts of free radicals. This is true of MSG and aspartic acid (40% of the aspartame molecule).
* There is substantial circumstantial evidence that dietary excitotoxins, including aspartame, can aggravate these destructive changes in the Parkinson's brain.
* The additional toxins - DKP, aspartate, methanol, formaldehyde and formic acid - add to this injury.
* Recent evidence demonstrates the aspartame product, formaldehyde - accumulates within cells and damages proteins and DNA.
Aspartame decreases the entry of methyldopa into the brain of rats (Timothy J. Maher and Paul J. Kiritsy)
H. J. Roberts, M.D., who declared Aspartame Disease to be a global plague published the medical text, Aspartame Disease: An Ignored Epidemic. He discusses that aspartame may either reduce or potentiate drug action by various mechanisms. Here are a few of the possibilities:
* Alteration of the blood proteins to which drugs attach.
* Alteration of drug receptors on cell membranes.
* Changes in the sites at which impulses are transmitted along nerves and to muscle.
* Metabolic abnormalities in the elderly that are known to enhance this vulnerability to drug reactions (Weber l986) This problem increases in the case of persons taking multiple drugs ("polypharmacy") prescribed by several physicians.
* Interference with drug action by amino acids and protein. An example is the erratic therapeutic effects when patients with parkinsonism who were controlled on levodopa began to use aspartame products. The antagonism of levodopa by dietary protein presumably reflects impaired transport from serum across the blood brain barrier by neutral amino acids (Pincus l986).
Dr. Roberts discusses pathophysiologic considerations. There is an alteration of serotonin and dopamine concentrations in the brain by phenylalanine and aspartame. The following observations are germane.
* The enzyme phenylalanine hydroxylase converts phenylalanine to tyrosine. Tyrosine is first transformed into dihydroxyphenylalanine (levodopa), and then to dopamine.
* The two dopamine receptor subtypes (D1 and D2) exert synergistic effects on the firing rates of basal ganglia neurons (Walter l987)
* The importance of dopaminergic pathways in severe tremor is further suggested by the effectiveness of levodopa in treating both parkinsonism and "restless legs" (von Scheele l986)
* There is a reduction of brain dopamine in the presence of high concentrations of phenylalanine (Congressional Record - Senate l985b, p. S. 10846).
* Chronic exposure to excess phenylalanine and aspartic acid can decrease the levels of serotonin and other neurotransmitters within several regions of the brain. These changes, presumably compensatory adaptive mechanisms, may disturb important diurnal variations associated with feeding and the light/dark cycle.
* An ad by G. D. Searle & Company in the Journal of the American Medical Association (Dec 16, l986) implied that excess activity of these excitatory amino acids could cause nerve cell destruction resembling the changes in degenerative disorders of the nervous system.
I've been taking the case histories of aspartame victims for almost 15 years. There are repeated references to clinical deteriation and erratic therapeutic responses when patients with parkinsonism ingest aspartame products. Consider Michael Fox, a Diet Pepsi spokesman, who said: "How could I get an old man's disease, Parkinson's, at the age of 30?" He is known to be addicted to aspartame pop.
Dr. Blaylock says in Excitotoxins that glutamate, amphetamines and other excitotoxins may produce Parkinsonism by overexciting the cortical glutamate cells that connect to the nigrostriatal neurons lying deep in the brain. This is also true of aspartame. He says it is sort of like lightning hitting the power line outside your house and burning up all of the appliances connected to that line. The power line represents the cortical glutamate neurons and the appliances, the nigrostriatal system.
James Bowen, M.D., wrote that many NutraSweet victims report Parkinsonian symptoms and says this should be no surprise because every biochemical component of the aspartame molecule is implicated in producing Parkinsonian structural damage and creating a biochemical basis for Parkinsonian symptoms.
He further said the structural damage in the basal areas of the brain where Parkinson Disease structural damage occurs from the dicarboxylic amino acid neuroexcitotoxins is a problem long recognized. So aspartic acid even in and by itself is a recognized source of the damage to the basal ganglia where Parkinson Disease degeneration occurs. As in the case with methyl alcohol the molecular structure of the aspartame molecule probably makes the aspartic acid damage from aspartame 5000 times more potent than from free aspartic acid on a mg. per mg. basis. The brain with loss of neural tissue to produce the dopamine, a neurotransmitter necessary to let the brain circuitry function normally, is no longer producing dopamine in sufficient amounts in these structures. The metabolic impact of the phenylalanine isolate from aspartame is to remarkably decrease dopamine production thus making Parkinson symptoms much worse.
The phenylalanine isolate out competes all other amino acids at enzyme sites in the brain. This includes the decarboxylase enzyme sites. Therefore, the amino acid tyrosine is not decarboxylated to tramine which is the first step in producing dopamine in the brain. Therefore, the brain dopamine levels plummet remarkably.
Dr. Bowen commented that Michael Fox has reportedly used L-Dopa to try and increase his dopamine levels. The use of aspartame completely defeats this therapeutic endeavor. Not to mention the fact it caused the degenerative disease in the first place.
There are many efforts to ban aspartame. Stephen Fox petitioned the Environmental Improvement Board and Pharmacy Board in New Mexico. There is now a bill to ban aspartame in the New Mexico legislature. Roger Williams, a member of Parliament has called for a ban in the UK, Robin Goodwin, Mission Possible Falkland Islands, has petitioned a ban there. His wife developed an aspartame brain tumor and his child suffered with seizures until she abstained from the toxin. Activists in other states are lining up to follow in the footsteps of New Mexico.
Aspartame should never have been approved. In fact, the FDA themselves revoked the petition for approval after efforts failed to have Searle indicted for fraud. Both U.S. Prosecutors hired on with the defense team. Donald Rumsfeld who was then CEO of Searle said he would call in his markers and get it approved anyway. James Turner, Atty, explains how he did in the aspartame documentary, Sweet Misery: A Poisoned World. Here is the clip:
Furthermore, aspartame interacts with all drugs and vaccines:
Dr. James Bowen has Lou Gehrigs triggered by aspartame. In this report on Lou Gehrigs it's easy to understand the mechanism by which it can also trigger Parkinson's Disease.
By Dr. Betty Martini
Mission Possible International
Telephone: 770-242-2599
Web Site: &
About this issue of Gulf War Illness and Lou Gehrigs, there was an article published in Neurology in September. Many articles have appeared about two studies.
Bob Mackle, Director of Public Information (News from MDA) said on March 10, 2003:
"ALS, also known as Lou Gehrigs disease, attacks the muscle controlling nerve cells called motor neurons, causing the muscles connected to them to waste away. There is no cure and many people with the disease succumb to respiratory failure within three to five years of diagnosis. A new study published on-line by Nature Genetics shows that genetic defects affecting a supply line within motor neurons can lead to an ALS-like disease."
So what does aspartate (excitotoxin in aspartame) do? On the back cover of Dr. Blaylock's book it gives the definition of an excitotoxin: "A substance added to foods and beverages that literally stimulates neurons to death, causing brain damage of varying degrees. Can be found in such ingredients as monosodium glutamate, aspartame (NutraSweet), cysteine, hydrolyzed protein, and aspartic acid." (Excitotoxins: The Taste That Kills)
A neuron, of course, is a nerve cell, the structural and functional unit of the nervous system. It consists of a cell body and its processes, an axon, and one or more dendrites. Neurons function in initiation and conduction of impulses.
Now we're interested in the motor neurons, and there is upper and lower. In the upper this is neuron whose cell body lies in motor areas of cerebral cortex. Its axon passes down the spinal cord and synapses with lower motor neurons.
We know aspartame damages DNA and we know it destroys neurons. Dr. James Bowen, of course, explained it so it's easy to understand. And he said: "Aspartic acid, the excitotoxic component of aspartame does not cross the blood brain barrier but is secreted into the cerebral spinal fluid by the choroid plexus located in the ventricles of the brain. There, in the brain's lower area and upper terminus of the spinal is where Lou Gehrigs, Parkinson's Disease and Multiple Sclerosis damage is most prominent. These critical locations are bathed in the toxin as it removes from the blood. From the third to fourth ventricle there is a narrow canal called sylvian aqueduct which fills with this secretion and washes the roof of the hypothalamus."
In Mackle's article he discusses a 1999 study and mentions that disruptions of axonal transport perhaps by toxins might be capable of triggering sporadic ALS. Aspartate and glutamate can be that toxin. Incidentally, MDA is a voluntary health agency working to defeat more than 40 neuromuscular diseases through programs of worldwide research. "Two new studies appearing in the journal Neurology, one privately funded, the other federally supported, both report an above-average occurrence of amyotrophic lateral sclerosis among Persian Gulf War deployed veterans." (Sept 23rd issue)
"A privately funded study by Robert W. Haley of the University of Texas Southwestern Medical Center in Dallas and a government-funded study by Ronnie D. Horner of the National Institute of Neurological Disorders and Stroke in Bethesa, Md., both depict a roughly two fold risk of ALS development for U.S. veterans who were actively deployed in the Persian Gulf between August 2, 1990, and July 31, 1991, when compared with nondeployed U.S. military personnel."
"With deployed troops developing ALS more frequently and, maybe more importantly, much earlier in life than average, the two studies raise the question of whether an environmental factor could have triggered an early onset of the disease."
One thing we have to keep in mind, aspartame knows no age and the geography makes no difference. In the Persian Gulf at that time the troops were consuming lots of diet pop cooking in the 120 degree Arabian sun for as long as 8 weeks at a time, according to vets I personally interviewed in Huntsville, Alabama.
Remember Time Life published an article on bipolar, well know to be triggered by aspartame because of the depletion of serotonin. But the article was interesting in that this is an adult disease and children were developing Bipolar. (40% of children in the US are using it). Michael Fox wanted to know why he developed Parkinson's, an old man's disease, when he was only 30. He was a Diet Pepsi spokesmen and addicted to it. The Alzheimer Association says 50% of all nursing home beds have Alzheimer patients, including mature baby boomers. A hospice nurse told me they were getting 30 year olds with Alzheimers, and aspartame is escalating this disease. (Defense Against Alzheimers Disease, H. J. Roberts, M.D.)
And so with ALS - Mackle continues: "In addition to a higher incidence of ALS in Gulf War vets, the studies both show a higher than average occurrence of ALS onset in people in their 20s and 30s. Because ALS typically occurs in middle age, the studies hint at the possibility of an environmental agent that triggers ALS prematurely."
So what environmental agent triggers ALS prematurely? Aspartame! How long has it been known that aspartame triggers ALS? Dr. Bowen wrote the FDA 19 years ago: "Aspartic acid is a neuroexcitotoxic present in damaging amounts, in its own right at the ADI for aspartame. Simple logic tells one that it will vastly increase the metabolism of methyl alcohol to formaldehyde ... This corresponds well with the symptomalogies often experienced, such as LOU GEHRIG'S DISEASE (ALS), bulbar palsies, neurohormonal disorders. ..Diketopiperazine issue remains totally unresolved and dangerous."....
Neurosurgeon Russell Blaylock, M.D., wrote Excitotoxins: The Taste That Kills about diseases triggered by such excitotoxins as MSG and aspartic acid. He quotes Dr. John Olney pointing out the irony of a food industry practice:
"Thus, today we are witnessing an ironic situation; while knowledgeable neuroscientists are fervently attempting to develop methods for protecting CNS (brain) neurons against neurotoxic potentials of endogenous Glu (glutamate) and Asp (aspartate), other elements of society are vigorously promoting the unlimited use of exogenous Glu and Asp as food additives."
"Today the experimental evidence demonstrating the neurotix potential of these excitotoxins is so overwhelming, as can be seen from the scientific citations in this book, that it can no longer be ignored."
Dr. Blaylock explains how excitotoxins work. "The studies showing how excitotoxins work have greatly increased our understanding, not only of brain function, but also of the very basis of the degenerative brain disease process itself. In this discussion you must keep in mind that the excitotoxins added to food are the exact same ones that produce experimental brain damage in animals. And the glutamate in our discussion is the same substance and active ingredient found in MSG. The neurotoxin aspartate is a major component in the artificial sweetener aspartame (actually a mixture of two amino acids, phenylalanine and aspartate, and methanol or wood alcohol)."
He says further: "Both glutamate and aspartame can cause neurons to become extremely excited and, if given in large enough doses, they can cause these cells to degenerate and die."
There is a chapter in this book titled Creeping Death: The Neurodegenerative Diseases. Here are some comments that help to explain.
"By ingesting diets high in MSG, hydrolyzed vegetable protein, aspartame and other excitotoxins, these people would be exposing their brains to damaging levels of this class of toxin. Eventually other neurons would be damaged, possibly leading to symptoms of Alzheimer's type dementia and ALS."
Remember what Dr. Bowen said about aspartic acid seeping into the brain. Dr. Blaylock says: "It's also possible that glutamate and aspartate can enter the brain without a breakdown in the blood brain barrier. We know that certain areas of the adult brain have no, or incompetent, barriers. These areas are near the ventricular system (circumventricular organs) and can potentially act as points through which glutamate and aspartate in the plasma could slowly seep into the surrounding brain, thereby by-passing the blood brain barrier."....
On page 118 Dr. Blaylock explains Amyotrophic Lateral Sclerosis: Lou Gehrig's Disease. He says: "Amyotrophic lateral sclerosis, also known as Lou Gehrig's disease, is a neurodegenerataive disease that primarily affects the anterior horn cells of the spinal cord. These are the primary neurons in the spinal cord that control muscle movements of the body. But these neurons do not operate by themselves, rather they are controlled from higher up in the brain by other neurons in the motor cortex which send fibers down the spinal cord, that in turn connect (synapse) with the anterior horn cells. This bundle of fibers from the cortex is called the corticospinal tract. In most cases of ALS these neurons are also affected."
Dr. Blaylock discusses research on ALS in l987 by Doctors Andreas Plaitakis and James T. Caroscio:
"In a follow-up study, Dr. Plaitakis and his coworkers examined the glutamate and aspartate levels from the cerebellar cortex, frontal lobe and two areas of the spinal cord in patients dying of ALS. They found that glutamate levels were significantly decreased (21 to 40% lower than controls) in all areas tested. The cervical and lumber cord, the areas containing the greatest number of motor neurons, showed the greatest deficit. Aspartate was significantly decreased in the spinal cord only (32 to 35%). This defect in the aspartate and glutamate pools in the brain and spinal cord of ALS patients could indicate that these specialized neurons are destroyed and as a result have lost their previously high concentrations of these excitatory amino acids."
Writing about the prevention of ALS he says: "You must also avoid all foods and drinks sweetened with aspartame (NutraSweet), since it contains the powerful excitotoxin aspartate. In addition, all that we have learned about hypoglycemia and Parkinson's disease also applies to ALS patients. Low energy level greatly magnify the toxic effect of MSG and aspartate on the spinal cord."
There are many interesting comments in this book relating to MSG and aspartame as follows: "Placebos are supposed to be completely inert substances. Otherwise the ywould produce a physiological effect all of their own and ruin the experiment. In the case of MSG toxicology studies, the placebo used to test the excitotoxin glutamate is NutraSweet, which contains the excitotoxin aspartate. It has been clearly shown in a multitude of studies that aspartate produces the identical destructive reactions on the nervous system as MSG. It would seem obvious even to the layman that you would not use a control substance to compare to a known toxin if the control contained the same class of chemical toxin. But that is exactly what is being done."
"Are the representatives of the glutamate industry aware of this basic scientific fact? It is hard to believe otherwise, especially in the face of the fact that one of their own representatives presented evidence before a public hearing at a meeting of the Federation of American Societies for Experimental Biology in which tables were presented showing that aspartame produces the same types and incidences of reactions as MSG."
"Did these scientists disclose in their scientific papers the fact that the placebos also contained a known excitotoxin? The answer is an emphatic "no", and I have reviewed dozens of these studies. In fact, I was not aware of this deception until I received the proof from Dr. Samuels. In many cases the powder used to mix the placebos was supplied by the International Glutamate Technical Committee (IGTC). It is interesting to note that the Ajinomoto company, the chief manufacturer of MSG and the raw materials of aspartame, is an active member of the IGTC."
"This company funds extensive research programs and provides funds to major universities for research on the safety of MSG. In my personal opinion, I have to believe that both the company representatives, and certainly the scientists doing the research, must know that such studies are dishonest at the very least."
Its obvious that aspartame can cause ALS. In conclusion Dr. Blaylock says: "..But of primary concern is the effect of these powerful brain cell stimulants have on the developing brain of the infant and child and the later development in the adult of neurodegenerative diseases such as Parkinson's disease, Alzheimer's dementia, Huntington's disease and ALS. The brain not only utilizes the excitatory amino acids as normal neurotransmitters, but there exists a delicate balance of excitatory and inhibitory chemicals in the brain. When the balance is upset, serious disorders of the nervous system can result."
If someone in the Aspartame Support said they were using lots of aspartame and suffered from memory lapses, fatigue, joint pains, rashes, headaches, dizzy spells and cancer you wouldn't think anything of it. These are known problems triggered by aspartame. What is the difference when they drink lots of aspartame already broken down to a witches brew of toxins in the Persian Gulf? Why would geography make a difference?
Richard Lieby, in the Dec 30 edition of the Washington Post, wrote: "The Pentagon says it still has no answer for an enigma that has confounded experts for more than a decade: What caused all the ... memory lapses, fatigue, joint pains, rashes, headaches, dizzy spells, cancer, Lou Gehrig's disease and birth defects" collectively known as Gulf War Syndrome?
And why don't the experts know? Could it be because the manufacturers of aspartame lie, the FDA lies and the professional organizations funded by the manufacturers lie. Dr. Blaylock in this book says so little of this information is known by the general public. Do you understand why I tell people these books on aspartame are important for them to have. They need to know it all because they certainly aren't going to find out by calling some of these organizations who sold out for 30 pieces of silver. And these doctors have paid a price. They did the research for us, and have battled to get the information to the public, since as I mentioned, it's very difficult to get it in medical journals, or in the mainstream media.
ALS or Lou Gehrigs is also in Dr. Roberts's medical text on page 244, Aspartame Disease: An Ignored Epidemic. He says the contributory role of aspartame to ALS was suspected in several instances. This association became more impressive when close relatives developed related neurologic disorders. He gives the case history - "A man with adult onset diabetes used considerable aspartame especially as a tabletop sweetener in his oatmeal and coffee. He developed severe and ultimately fatal ALS. Two daughters suffered severe aspartame disease, one having been initially diagnosed as multiple sclerosis."
Most of the vets I have interviewed over the years told me they drank diet drinks all day long. Here is what Dr. Blaylock says in Health & Nutrition Secrets To Save Your Life: .. "Using a radioactive tracer method, it has been clearly demonstrated that the formaldehyde formed from aspartame accumulates near the DNA in cells, resulting in numerous deletions and strand breaks in the nuclear material. Even more frightening is the finding that the damage is accumulative, so that even drinking one diet cola a day can produce significant genetic damage. There are also several reports of severe aspartame addiction, characterized by the daily consumption of a gallon or more of aspartame sweetened beverages." All it takes is drinking just one diet drink a day!!!!
And in this book Dr. Blaylock also goes into those diet drinks cooking in the hot Arabian sun in the Persian Gulf. He also says this: "So in the case of diet drinks in aluminum cans, the very toxic brain aluminum fluoride compound co-exists with multiple toxins found in aspartame, thus creating the most powerful government approved toxic soup imaginable."
About aspartame he says: "This particularly nasty substance should have never even been approved for human use. In fact, had it not been for some fancy footwork by those in power in the FDA it never would have."
In the Jan 7, 2003 article, Toxic Threat for Troops in New Gulf Way ( ), Robert McMahon of Soldiers for the Truth said: "A 100 hour ground campaign that saw 148 Americans KIA and 467 wounded in Gulf War 1 produced 159,238 veterans receiving a medical disability payment monthly. That is damn near 30 percent of our forces committed to the region at that time."
If these troops who served in the Persian Gulf had been warned about aspartame, and read the books by the experts, many would still be alive today. At last count, 40,000 had perished.
__________ End of this report
In July, 2005, the European Ramazzini Foundation of Oncology and Environmental Sciences Cancer Research Centre in Bolonga, Italy released their three year study confirming the link between aspartame and lymphomas and leukemias, dose related. In September at a conference they added cancer of the kidney and cancer of the cranial peripheral nerves, and declared aspartame a multipotential carcinogen. Only rats fed aspartame developed malignant brain tumors.
Neurosurgeon Russell Blaylock, M.D., one of the world's leading authorities on aspartame neurotoxicity extensively reviewed this report. "This study confirmed the previous study by Dr. Trocho and co-workers (l998), which also found the formaldehyde breakdown product of aspartame to be damaging to cellular DNA and that this damage was cumulative. The type of damage was a duplicate of that associated with cancers. These two studies strongly indicate that drinking a single diet cola sweetened with aspartame every day could significantly increase one's risk of developing a lymphoma or leukemia."
Dr. Blaylock continued "This study should terrify mothers and all those consuming aspartame sweetened products. This was a carefully done study which clearly demonstrated a statistically significant increase in several types of lymphomas and leukemias in rats. Both of these malignancies have increased significantly in this country since the widespread use of aspartame."
Aspartame has been on the market a quarter of a century and now we have a global plague. But it was known from the very beginning that aspartame is a carcinogen. The late Dr. M. Adrian Gross, FDA toxicologist, spoke out against aspartame in the August, l985 Congressional hearing. Gross, who took part in on-site investigations at Searle laboratories, said the studies carried out by Searle "to a large extent were unreliable." He said "at least one of those studies has established BEYOND ANY REASONABLE DOUBT that aspartame is capable of inducing brain tumors in experimental animals and that thus .. is of extremely high significance."
Gross testified because aspartame produces brain tumors and brain cancer, FDA should not be able to set an allowable daily intake of the substance at any level: "In view of these indications that the cancer causing potential of aspartame is a matter that has 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?"
The Delaney Amendment makes it illegal to allow any residues of cancer causing chemicals in foods. In his concluding testimony Gross asked, "Give 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?"
So the FDA has known for a quarter of a century aspartame violated the law and is not only a deadly neurotoxic drug but a carcinogen. The National Soft Drink Association, now American Beverage, even admitted that it violated federal adulteration statutes. <>
Aspartame can trigger birth defects and mental retardation and is an abortifacient. This is documented in medical texts by Doctors Roberts and Blaylock. No doubt millions have perished from it. When those responsible to solve the problem ARE the problem its a sad commentary on how the FDA has betrayed the trust of the people. And I find it difficult to understand how any pharmaceutical company would not know aspartame is a deadly neuroexcitotoxin after being on the market murdering victims for a quarter of a century. Any research would shout "deadly neuroexcitoxic carcinogen"! There are over 2 million sites on the Internet warning consumers because the FDA sold out to the manufacturers. And there are stacks of medical books, two of which I have quoted. How could you put this poison in a Parkinson drug? Did you do your research with a blindfold?
Most chemical sweeteners are not safe. Splenda is a chlorocarbon poison and Acesulfame Potassium caused cancer and leukemia in original studies.
Please advise immediately you are removing this toxin, otherwise be responsible for every death it causes. James Bowen, M.D. says aspartame violates Title 18, the Federal Domestic Genocide law:
Dr. Betty Martini
Founder, Mission Possible International
9270 River Club Parkway
Duluth, Georgia 30097
Aspartame Toxiocity Center:



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