- This is a letter published with the permission of Dr.
Betty Martini, D.Hum, Founder of Mission Possible International to Hawaii
Senate Health Chair, Sen. David Ige, who although signed the Hawaii Senate
Resolution asking FDA to rescind approval for aspartame, ended up in fact
never scheduling it for the obligatory hearing in his Senate Health Committee,
thus killing the Resolution that he had signed with ten other Senate Committee
Chairs and Vice Chairs!
- April 28, 2008
- Dear Senator Ige:
- The Senate Resolution, SCR 191, regarding aspartame,
was so damning, you felt it had to be a hoax, and requested references
which were immediately sent. Even this short resolution as damning as it
was about this deadly addictive excitoneurotoxic carcinogenic drug that
interacts with virtually all drugs and vaccines could not convey every
- Many years ago I met a woman who had met one of the three
scientists who had worked on the project. He was known to travel telling
people to avoid NutraSweet at all costs because it should never have been
approved. He was also on the Phil Donahue show back in the early l980's
explaining how aspartame is a seizure triggering drug, and anti-seizure
medication won't work. He had pleaded with Searle not to approve this
deadly drug and finally left in disgust. I was very concerned with the
fact the woman said that he was elderly and admitted he might not live
to see the day when people would just be dropping dead in the streets from
aspartame. Today that is happening.
- So many athletes have dropped dead that Dr. Russell Blaylock,
author of Excitotoxins: The Taste That Kills, www.russellblaylockmd.com
wrote a warning. Here is that Athlete Alert: http://www.wnho.net/aspartame_msg_scd.htm
Dr. H. J. Roberts who wrote the 1000 page medical text, Aspartame Disease:
An Ignored Epidemic, www.sunsentpress.com likewise wrote a paper on Aspartame
and Sudden Death: http://www.wnho.net/aspartame_and_arrhythmias.htm Here's
one I wrote as well to the FDA: http://www.wnho.net/openlettertofda.htm
Some years ago two European Parliamentarians petitioned the World Health
Organization because they couldn't understand why people were dropping
dead for no reason. They suggested it should be called sudden death syndrome
so it could be tracked. Even young student athletes in schools are dropping
- Do not think that Searle who originally made this poison
doesn't know how deadly aspartame is. First of all, pharmaceutical and
chemical companies are known to do studies out of the country to find out
how damaging products are they are concerned about. In the case of aspartame
Searle did studies in six countries sacrificing people in poor villages
who wouldn't be missed. An affidavit from the translator explained how
aspartame destroyed the brain and central nervous system. She said subjects
in 18 months got brain tumors and had all types of seizures, and aspartame
hardened the synovial fluids. The pregnant woman lost her baby, hemorrhaged
and then disappeared. Some died.
- Searle was very good at telling people that aspartame
is the most studied product and 200 studies have been done showing safety.
What Searle didn't say was that in these studies they couldn't prove safety
so they committed fraud, and they got caught. Here is the Bressler Report
or FDA audit which explained how Searle was filtering out neoplasms, and
they were even excising brain tumors from the rats, putting them back in
the study and then resurrecting them on paper. The report found that 98
of the 196 animals died during one of Searle's studies and weren't autopsied
under later dates, in some cases over one year after they died.
- Records for approximately 30 animals showed
substantial differences between original observations on pathology sheets
and the observations on pathology sheets submitted to the FDA. There were
numerous other inconsistencies and errors noted. A mass, a uterine polyp
and ovarian neoplasms were found in animals but not reported or diagnosed
in Searle's reports. The FDA investigators found dose-related uterine
polyps in 15% of 34 animals. Interestingly I called Jerome Bressler when
he retired from the FDA and thanked him for being honest and telling the
public the truth. He told me that it was a lot worse than what I had read
in the FDA audit because the FDA had retyped his report and it was so damning,
they left out the worst 20%, two mice studies. Doctors H. J. Roberts and
Russell Blaylock also spoke with Jerome Bressler and were told the same
thing so Dr. Roberts asked his Congressman to get the omitted part of the
report. The FDA refused the congressman saying it was confidential. I
recently wrote a FOIA report for it and was told it was confidential.
When I said that this audit was a matter of public record all of a sudden
it became destroyed. http://www.mpwhi.com/fda_gate.htm
- On January 10, l977 in a 33 page letter, FDA Chief Counsel
Richard Merrill recommended to US Attorney Sam Skinner that a grand jury
investigate Searle for "apparent violations of the Federal Food, Drug,
and Cosmetic Act, 21 USC 331 (e) and the False Reports to the Government
Act 18 USC 1001, for "their willful and knowing failure to make reports
to the Food and Drug Administration required by the Act 21 U.S.C. 355 (i),
and for concealing material facts and making false statements in reports
of animal studies conducted to establish the safety of
- aspartame." Instead of indicting Searle, Sam Skinner
hired on with the defense team. So U.S. Prosecutor William Conlon was
asked to take over. He, too, hired on with the defense team and the statute
of limitations expired. http://www.mpwhi.com/drug_testing_falsified.htm
- The FDA at that time had absolutely no intention of allowing
aspartame on the market. Here are some remarks made at the FDA Task Force:
- "At the heart of FDA's regulatory process is its
ability to rely upon the integrity of the basic safety data submitted by
sponsors of regulated products. Our investigation clearly demonstrates
that, in the case of G D Searle Company, we have no basis for such reliance
- "We have noted that Searle has not submitted all
the facts of experiments to FDA, retaining unto itself the unpermitted
option of filtering, interpreting, and not submitting information which
we would consider material to the safety evaluation of the product ....
Finally, we have found instance of irrelevant or unproductive animal research
where experiments have been poorly conceived, carelessly executed, or inaccurately
analyzed or reported."
- "Some of our findings suggest an attitude of disregard
for FDA's mission of protection of the public health by selectively reporting
the results of studies in a manner which allay the concerns of question
of an FDA reviewer." "Unreliability in Searle's animal research
does not imply, however, that its animal studies have provided no useful
information on the safety of its products. Poorly controlled experiments
containing random errors blur the differences between treated and control
animals and increase the difficulty of discriminating between the two populations
to detect a product induced effect.
- A positive finding of toxicity in the test animals
in a poorly-controlled study provides a reasonable lower bound on the true
toxicity of the substance. The agency must be tree to conclude that the
results from such a study, while admittedly imprecise as to incidence or
severity of the untoward effect, cannot be overlooked in arriving at a
decision concerning the toxic potential of the product."
- It would be very easy to give you another 50 pages of
the horrors of original aspartame studies. You simply can't take a deadly
chemical poison and have it show safety. It can't be done. Searle got
- For instance in the aspartame (DKP) 115 week rat study
the written observations of the pathology report was changed by the supervising
pathologist, Dr. Rudolph Stejskal even though he was not physically present
during the autopsies and could not have verified the observations of the
pathology who did perform the autopsies. The pathologist who did perform
some of the autopsies had no formal training for such procedures. (Gross
l985, page S10837 of Congressional Record l985b). You could go from study
to study and show the fraud. For instance in the aspartame 46 week hamster
study, blood samples reported in the submission to FDA as 26 week values
(for certain specified animals) were found by investigators as being, in
fact, values for different animals which were bled at the 38th week. Many
of the animals for which these values were reported (to the FDA) were dead
at the 38th week." (Gross 1985, page S10838 of congressional record
- There were "clerical or arithmetic errors which
resulted in reports of few tumors." (Schmidt 1976c, page 27 of US
Senate l976b). G. D. Searle "delayed the reporting of alarming findings."
(Schmidt 1976c, page 27 of US Senate 1976b).
- Dr. Adrian Gross, FDA toxicologist who was on site really
summed it up when he said:
- "They ( G.. D. Searle) lied and they didn't submit
the real nature of their observations because had they done that it is
more than likely that a great number of these studies would have been rejected
simply for adequacy. What Searle did, they took great pains to camouflage
these shortcomings of the study. As I say filter and just present to the
FDA what they wished the FDA to know and they did other terrible things
for instance animals would develop tumors while they were under study.
Well they would remove these tumors from the animals." Wilson l985
- FDA lead investigator and Task Force Team Leader, Phillip
Brodsky described the 1975 FDA Task Force members as some of the most
experienced drug investigators. He went on to state that he had never
seen anything as bas as G. D. Searle's studies (Graves 1984, page S5499
of Congressional Record l985a).
- Dr. Marvin Legator, professor and director of environmental
toxicology at the University of Texas and the pioneer of mutagenicity testing
at the FDA from 1962 to 1972 was asked by Common Cause Magazine to review
the FDA investigation results of G. D. Searle's tests (Graves 1984, page
S5498 of Congressional Record 1985a):
- "All tests were scientifically irresponsible and
disgraceful. I'm just shocked that that kind of sloppy work would even
be sent to FDA, and that the FDA administrators accepted it. There is
no reason why these tests couldn't have been carried out correctly. It's
not that we are talking about some great scientific breakthrough in methodology."
- Senator Edward Kennedy at the April 8, 1976 hearings
before the Senate Subcommittee on Labor and Public Welfare stated (Kennedy
l976): "The extensive nature of the almost unbelievable range of
abuses discovered by the FDA on several major Searle products is profoundly
- Senator Ige, this is what we know: no doubt a lot was
hidden. In fact, Dr. Adrian Gross said the deliberate misconduct and lies
invalidated all their experiments for these reasons:
- 1. Many of the problems with the studies included horrendous
experimental designs, questions regarding dosage given, loss of animal
tissue and data, etc.. which invalidates entire experiments and causes
what they claim to be 4 million observations and calculations per study
(average) to become irrelevant.
- 2. Only the key aspartame studies were looked at. It
is almost a certainty that the non-key aspartame studies were equally flawed.
Therefore, this would invalidate the "hundreds of millions"
of observations and calculations made during these studies.
- 3. The difference between a study showing no statistical
difference and a significant statistical difference is often only a few
observations or calculations. Therefore, had the myriad of other serious
experimental errors not occurred, the observation and calculation mistakes
in each experiment investigated would, by themselves, invalidate most of
the key studies.
- 4. It is highly unlikely that the FDA Investigative
teams found all of the problems with G. D. Searle's studies. G. D. Searle
seemed so intent on covering up their misconduct, that it is quite likely
that they were able to hide many of the problems from the FDA.
- So you see, Senator Ige, no matter what the aspartame
industry says, about aspartame being the most tested additive in history
and showing safety, the public record shows aspartame never showed safety
at all. What it did show was massive fraud, and they got out of it by
buying the U.S. Prosecutors who were never investigated for not doing their
job and instead going to work for the defense team.
- So FDA revoked the petition for approval. Here is that
- Before the FDA Commissioner, Dr. Jere Goyan could sign
this into law, the next day Searle filed suit. Don Rumsfeld was CEO of
Searle, hired to get them out of trouble. He said he would call in his
markers and get aspartame on the market anyway. What were those markers?
President Reagan had told Rumsfeld he would nominate him for Vice President
but instead nominated Bush. Rumsfeld said Reagan owed him a favor and
Reagan paid it. Rumsfeld was on Reagan's transition team and the day after
President Reagan took office he appointed Dr. Arthur Hull Hayes as FDA
Commissioner to over-rule the Board of Inquiry. Knowing it would take
30 days to get him there he wrote an executive order making the FDA powerless
to do anything about aspartame. This executive order is suppose to be
a matter of public record but today has been stricken. Someone from the
Reagan Transition Team called FDA Commissioner, Dr. Jere Goyan at 3:00
AM in the morning and fired him. Here is the actual letter from Dr. Goyan's
wife who at the time was with him when he received the call. Notice she
mentions that executive order. www.mpwhi.com/letter_about_goyan.pdf
- Dr. Goyan died just a few months ago.
- Back during those days the FDA was the hero. A former
Searle employee once wrote an article titled: "What Happened To the
Old FDA?" Her question was answered by the Philadelphia Inquirer
on 11/22/87: The New FDA: Good Medicine for Drug Firms: http://www.mpwhi.com/the_new_fda.htm
This is when as the article points out the FDA stopped operating in an
adversary role and became a friend of the drug industry. This is the
FDA under Dr. Arthur Hull Hayes who was put there specifically to put one
of the most deadly drugs on the market to mass poison the American Public
and today over 100 countries of the world. Rumors fly on what they had
on Hayes to get him to do this deadly deed. When he over-ruled the Board
of Inquiry and put aspartame on the market he has refused to speak to the
press ever since.
- In l983 the National Soft Drink Association protested
that aspartame not be approved in carbonated beverages even mentioning
the law that makes it illegal to market a product that is adulterated.
They had concluded that aspartame is not safe in carbonated beverages.
- On July 8, l983 Acing Commissioner of the FDA, Mark Novitch,
approved NutraSweet for use in carbonated beverages and carbonated beverage
syrup bases, even though levels of aspartame remaining in beverages stored
eight weeks at 68 degrees F were between 84% and 89% of the original amount.
"Lost" aspartame degrades to DKP (a brain tumor agent), methanol,
a severe metabolic poison, aspartic acid, an excitotoxin, and phenylalanine,
as an isolate a neurotoxin that lowers the seizure threshold and depletes
serotonin triggering psychiatric and behavioral problems. Aspartame interacts
with all antidepressants.
- I personally called Mark Novitch recently and asked him
about what he did. It seems Mr. Novitch, who did this under the direction
of Arthur Hull Hayes, had a bad case of amnesia. He said it was so long
ago he just couldn't remember anything on the issue. That was certainly
a convenient loss of memory. Memory loss is #9 on the FDA list of 92 documented
symptoms from aspartame from four types of seizures to coma and death.
- Amid allegations of using General Foods jet and other
things, Dr. Hayes resigned and went to work for the PR Agency of the manufacturer
on a ten year contract for $1000.00 a day. What does an FDA Commissioner
do for a PR agency? Send postcards home from Bermuda. One article said
he was there about 15 days. Quite a reward for putting a deadly poison
on the market and mass poisoning the world so Searle could get rich. Immediately
people started complaining and Senator Howard Metzenbaum tried for congressional
hearings. They were not heard until 1985 because of Senator Orrin Hatch
who was given money from Monsanto who bought Searle that year.
- There were actually three congressional hearings because
of the outrage of the public on being poisoned. It was triggering seizures,
MS and all sorts of neurodegenerative diseases. One pilot who testified
said his plane started going down when he passed out over the sea on aspartame,
but woke up in time to land it. Mission Possible Aviation was started
when a plane crashed on aspartame, and the pilot came to Atlanta and asked
me for help. Here is Dr. Blaylock's pilot alert: http://www.mpwhi.com/pilot_aspartame_alert.htm
Notice he mentions again this problem of sudden death. Six American Airline
pilots died who used aspartame including one in flight, who passed out
and never woke up.
- Many scientists as well as victims testified and it was
admitted that the FDA was so overcome with complaints they were sending
them to the AIDS Hotline. Senator Metzenbaum wrote a bill to do independent
studies by the National Institute of Health having to do with the problems
being seen in the population. This included seizures, drug interaction,
behavioral problems and what it does to the fetus.
- Dr. Louis Elsas testified and said: .... I am a pediatrician,
a Professor of Pediatrics at Emory, and have spent 25 years in the biomedical
sciences, trying to prevent mental retardation and birth defects 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 both reversibly in the adult and irreversibly in the
developing child or fetal brain, produce adverse effects. You remember
those sloppy studies by Searle. So what about reproduction studies in
teratology to find out what aspartame would do to the fetus? Here is what
was discussed in Congress.
- "It is significant to note that the Searle employee
responsible for reviewing most of the reproduction studies had only one
year of prior experience, working on population dynamics of cotton trial
rabbits while employed by Illinois Wildlife Service. In order to prepare
him for this title of 'Senior Research Assistant in Teratology' (fetal
damage) Searle bought him books to read on the subject and also sent him
to a meeting of the Teratology Society. This qualified him to submit 18
of the initial tests to the FDA, in addition to training an assistant and
2 technicians. He certainly must have kept them busy because Searle claimed
that 329 teratology examinations were conducted in just 2 days. He estimated
that he himself examined about 30 fetuses a day, but officials for the
Center for Food and Applied Nutrition could never determine how that was
possible." Graves 1984, page S5500 of Congressional Record l985a).
- Since aspartame was approved autism has gone through
the roof. One woman who used Diet Coke with aspartame through 3 pregnancies
has 3 autistic children. Another woman said she stopped using aspartame
once pregnant but said her physician at Emory said it built up in her system.
She has one autistic child and one with ADD. Today between learning problems
and behavioral and psychiatric problems because of this poison our children
are medicated instead of educated. A Parents Magazine article in September
1999 said the normal for children today is abnormal.
- Senator Metzenbaum in his bill also asked that a moratorium
be put on aspartame. The bill never got out of Congress. One physician
who testified said Senator Orrin Hatch was a hypocrite and prevented anything
from happening. Congress is supposed to be there for the good of the people
and obviously doing independent studies on aspartame couldn't hurt anybody
but the manufacturer. Nobody in Congress cared about the people since
nothing was done during all three congressional hearings with physicians,
scientists and victims speaking out on the deadly effects of this drug.
Only Monsanto benefited who paid Orrin Hatch and others and made sure
- Both FDA toxicologists Dr. Adrian Gross and Dr. Jacqueline
Verrett who were on site and saw what happened in original studies spoke
out against the FDA who is today, Big Pharma's Washington Branch Office.
- On August 1, l985 the FDA's own 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?"
- The Delaney Amendment makes it illegal to allow any residues
of cancer causing chemicals in foods. In his concluding testimony Gross
asked, "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 SID835:131 (August 1, l985)
- Dr. Jacqueline Verrett told Congress she belied the original
aspartame studies were "built on a foundation of sand". She
testified in front of a U.S. Senate hearing in 1987 that flawed tests conducted
by Searle - used as the basis of FDA approval were a "disaster"
and should have been "thrown out". She said she believed the
studies left many unanswered questions about possible birth defects and
the safety of aspartame. Verrett said the team was instructed not to be
concerned with, or comment upon, the overall validity of the study. She
said a subsequent review discarded or ignored the problems and deficiencies
outlined by her team's original report. She said, "serious departures
from acceptable toxicological protocols, which her investigative team noted
in the reevaluation of these studies were also discounted. She warned
that any of the improper practices would compromise and negate a safety
study of food additive. Verrett concluded the data in the study was worthless,
and the safety of aspartame and its breakdown products have therefore not
- She emphasized that aspartame exists in the marketplace
without basic toxicity information. She said there are no data to assess
the interactions with DKP, excess phenylalanine, other aspartame metabolites,
additives, drugs or other chemicals. In her testimony, Verrett elaborated
on DKP problems, including significant increases of uterine polyps and
changes in blood cholesterol. Senator Metzenbaum, chairman of the hearing
when Verrett testified, asked her if she disagreed with FDA's position
that tests for aspartame safety were credible. Verrett succinctly said
- So even in 1987, 6 years after approval, aspartame had
still not been proven safe. In fact, in l986 the Community Nutritional
Institute in Washington, D.C. petitioned the FDA to ban aspartame because
so many people were having seizures and going blind from the free methyl
alcohol. The FDA refused. Remember today the FDA is part of Big Pharma.
When those responsible to solve the problem ARE the problem its a disgrace
and an abomination.
- As people continued to have seizures and other problems
Monsanto would fund studies to show safety. Here are examples of scientific
abuse in aspartame seizure studies: http://www.dorway.com/wurtman2.html
- Because its impossible to show safety of a poison like
aspartame, Dr. Ralph Walton did research on scientific peer reviewed studies
and funding. This showed that 92% of independent studies showed the problems
and only those funded and controlled by the manufacturer ever said they
were safe. In fact, Dr. Walton says if you eliminate 6 studies that the
FDA had something to do with because of their obvious siding with industry
now, and one pro-industry summary, that 100% of independent scientific
peer reviewed studies showed the problems aspartame causes. This proves
if the aspartame industry keeps their checkbook and influence out of it,
there is no way to get : http://www.dorway.com/peerrev.html
- FDA has betrayed the public trust. Today it has ignored
100 independent scientific peer reviewed studies including the Trocho Study,
which showed that aspartame embalms living tissue and damages DNA. When
you damage DNA you can destroy humanity. Dr. Alemany who sent testimony
to Hawaii told me personally in Barcelona that aspartame could kill 200
million people. The NutraSweet people when this study was done tried to
assassinate his character. Funding was immediately reduced. There is
a company called ILSI who gives funding with members like Monsanto, Searle,
Coke, Pepsi, etc., (that is: as long as you're willing to say this poison
is safe). FDA has also ignored a petition for ban for 6 years even though
the law requires they answer it in 180 days. Why haven't they answered
it, because the facts in the petition are from their own records and how
do you disagree with that. An imminent health hazard petition must be answered
within a couple of weeks. I sent this in October. They have ignored that
- My Senator told me if you want to ban aspartame is has
to go through the local legislature. First we tried New Mexico. The Capital
was saturated with lobbyists and front groups like Calorie Control Council
who even push aspartame on pregnant women. Some of the Senators I testified
too sat there sipping Diet Coke.
- Aspartame is addictive, the free methyl alcohol, classified
as a narcotic causes chronic methanol poisoning. This affects the dopamine
system of the brain and causes addiction. I happened to ask Dr. Bill Deagle
one day why addicts on aspartame were not rational. He said because aspartame
affects the frontal lobe so its like talking to someone who has had a lobotomy.
- Aspartame changes brain chemistry and users many times
can look at the documents that show the devastating studies and the horrors
aspartame caused, and insist its safe. It goes beyond dumbing down the
public. I've heard many of the experts say today the mental hospitals
are full of patients who are simply aspartame victims.
- Aspartame is pushed on diabetics when, in fact, it can
precipitate the disease, simulates and aggravates diabetic retinopathy
and neuropathy, destroys the optic nerve, causes diabetics to go into convulsions
and even interacts with insulin. Look at the epidemic of diabetes in Hawaii.
The aspartame manufacturers fund the American Diabetes Assn and professional
organizations in general. Look at Hawaii's epidemic of suicide. The phenylalanine
in aspartame depletes serotonin triggering suicidal tendencies, bipolar,
panic attacks, hallucinations, etc.
- Rep Josh Green, M.D. has the 1000 page medical text of
the horrors that aspartame triggers. It would take volumes to go over
the many symptoms and diseases. Just think of it, Senator Ige - planes
crashing, mental hospitals full of aspartame victims, lives destroyed,
diabetics dying, and people everywhere getting cancer. The prestigious
Ramazzini Studies showed aspartame is a multipotential carcinogen even
in small amounts, and passed on to other generations.
- Well Hawaii had its chance, didn't it, but lets just
talk about you for a moment, Senator. I've called you time and time again.
It's as if your assistant, Joyce, has been told to tell all people you're
in and out of committee meetings. You never return a call no matter how
many times calls are made, if its about aspartame. Even Dr. Deagle called
and you know he is almost in Hawaii now, and you didn't even have the decency
to return his call. Joyce has the habit of asking anyone who is not from
Hawaii just what they are doing about aspartame wherever they are from
and why they are concerned about this state. Is this what you told her
- The reason I'm getting on your case because you signed
the resolution and then decided it showed aspartame to be so deadly you
had to have references. When given the references so you knew beyond a
shadow of a doubt its all true, you did not set up the committee meeting,
and the original bill was deferred. Neither have you answered any of my
letters, not one, even though I took the time to give you what you asked
- So now I want to know who got to you? Was it aspartame
lobbyists, Coke or even Roz Baker who was deleting testimonies without
reading them? She was a previous lobbyist.
- Or Senator is it because you use the poison and want
to continue your habit? As I write this letter, Dr. Deagle is on his way
to Hawaii for a press conference we are hoping will be held. What will
you say to him when he gets there on the last day of the legislature?
Or will you ignore him too like you have ignored everybody else.
- Neither did Codex ban aspartame even though there were
great efforts. This means instead of 6000 products it could be in 100,000
products. Aspartame can destroy the human race, and the world you leave
for your children and your grandchildren. The only hope is for the states
that ban it, and you turned away from your responsibility to the people
of Hawaii. Every time somebody drops dead or gets cancer from aspartame
in Hawaii, remember: it didn't have to be that way. You had the opportunity
to stop it there and save the Hawaiian people from this poison. You wouldn't
even schedule the hearing! I'm disappointed and ashamed of you, Senator.
- There have been many heroes who gave their all like the
experts who have alerted the public for years. Attorney James Turner worked
with world renowned Dr. John Olney to prevent approval. Dr. Olney's 49
page report to the FDA gave the prophecy of how aspartame if approved would
destroy the brains of our children. Here is that report: <http://www.wnho.net/dr_olney1.doc>http://www.wnho.net/dr_olney1.doc
The FDA agreed and revoked the petition for approval, and then Rumsfeld
got it on the market. Unfortunately, the prophecy has now been fulfilled.
- What will you do now, Senator, as the legislature comes
to an end, and the hope with it to save the Hawaiian people from this poison?
Your assistant Joyce wanted to know why people from other parts of the
world cared about Hawaii. Because Senator, we are to love our neighbor
as ourselves and care about all people. It would have been commendable
if you had cared as much as people calling from around the world.
- Dr. Betty Martini, D.Hum, Founder
- Mission Possible International (warning the world off
- global unpaid volunteer force)
- 9270 River Club Parkway
- Duluth, Georgia 30097
- 770 242-2599
- www.dorway.com and www.holisticmed.com/aspartame