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Very Personal Testimony on Aspartame for Hawaii Legislators, particularly on fraudulent testing used for approval

By James Granger III, M.D.  Posted by Stephen Fox (about the submitter)       (Page 1 of 3 pages)   1 comment
Message Stephen Fox
Dr. James R. Granger III, MD
P.O. Box 681 Grovetown, Georgia

Feb 10 2008

Honorable Josh Green, MD
Honorable John Mizuno

Re: House Bill 2580 Room #329

Please Copy as Committee handout


I am a physician and truly disturbed by the continued availability of Aspartame in our food supply. As a resident physician I developed tremors in my dominant hand (right). These tremors affected my surgical performance to the point of having one of my professors inquire as to whether or not I had an alcohol problem.

I can assure you that I do not, nor have I ever had a substance abuse problem of any kind. My tremors persisted beyond my postgraduate training. I then had friends comment on noticing my hand shaking at rest outside of a clinical environment. After removing Aspartame from my diet, the tremors have been absent for over two years.

I have researched the issue and found that there is a plethora of scientific evidence to substantiate the claim that Aspartame should have never been allowed to enter our food supply.

Several facts need to be noted:

1) The FDA commissioner overruled his advisory board in 1983 to allow Aspartame into our food supply.
2) There is NO nutritional value to Aspartame.
3) The symptoms of Attention Deficit Disorder ( ADD) are contained within the list of complaints symptoms presented to the FDA regarding Aspartame
4) The incidence/diagnosis of Obesity, malignant tumors, ADD, anxiety and other diagnosis have all increased in epidemic proportions since the 1983 introduction of Aspartame into the food supply.
5) Many of the original studies were manipulated and poorly

Note the summary below ( excerpt from posted 3/12/2004): A few of the relevant findings summarized from various documents describing the FDA Task Force Report:

* "Excising masses (tumors) from live animals, in some cases without histologic examination of the masses, in others without reporting them to the FDA." (Schmidt 1976c, page 4 of US Senate 1976b) Searle's representatives, when caught and questioned about these actions, stated that "these masses were in the head and neck areas and prevented the animals from feeding." (Buzzard 1976a) "Failure to report to the FDA all internal tumors present in the experimental rats, e.g., polyps in the uterus, ovary neoplasms as well as other lesions." (Gross 1987a, page 8).

* G.D. Searle "stored animal tissues in formaldehyde for so long that they deteriorated." (Gordon 1987, page 496 of US Senate 1987; US Schmidt 1976c, page 25, 27 of US Senate 1976b)

* "Instead of performing autopsies on rhesus monkeys that suffered seizures after being fed aspartame, the company had financed a new monkey seizure study with a different methodology that showed no problems." (Gordon 1987, page 496 of US Senate 1987)

* "Reporting animals as unavailable for necropsy when, in fact, records indicate that the animals were available but Searle choose not to purchase them." (Schmidt 1976c, page 5 of US Senate 1976b)

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