DECLARATION CONTENTS

1. Top Nuclear Scientist states: We are on the Eve of Destruction…..we cannot survive even a small nuclear conflict - 138-146
2. Constitutional Rights Abolished by the Department of Justice & Judiciary (DOJJ) - 115-137
3. Corrupt Government and State officials cost the lives and quality thereof, of hundreds of thousands of U.S. citizens 1-30, 45-46
4. Precedent law and intent law has negated Legislative Law and the U.S. Constitution - 38, 105-108, 115-118, 120-126
5. The legislature lost its power to represent the people of the United States to the Department of Justice & Judiciary (DOJJ) 67, 103-121, 126-137
6. Total corruption in many Federal trials and appellate courts condoned by the Department of Justice & Judiciary (DOJJ) 25-48, 100, 115-126
7. Federal judges refuse trial by jury requests from defendants - 48, 124-125
8. Federal judges condone altering and tampering with Grand Jury documents - 27-29
9. Injustice for the majority of US citizens by the DOJJ - 50-52, 79-85, 97-102
10. DOJJ boasts over 95% conviction rate of innocent and guilty via plea bargains and conjured trials 30-48, 78-85, 100-101, 123, 124
11. Torture and death at the hands of the Department of Justice & Judiciary (DOJJ) 53-76, 84, 85, 87-92, 96-99, 103
12. Suggested laws need to be implemented and parole reinstated immediately to stop needless torture and death of inmates at the hands of the Bureau of Prisons (BOP) and DOJJ - 113-114
13. The Office of the Inspector General (OIG) whitewashes their investigations into the illegalities, inhumane treatment of prisoners under their control after a direct request from Senator Charles Grassley of the Judiciary Committee 87-96, 104, 130-131

"EVIL THRIVES WHEN GOOD PEOPLE DO NOTHING"

Writer: James T. Kimball Past President Discovery Experimental And Developmental, Inc., Past President ASTAK, Inc., Past President Global Health Information & Medical Research Institute, Inc., Past President B&B Freight Forwarding, Inc., Past President Discovery Tour Wholesalers, Inc., Past President American Transportation, Inc.

James Kimball has passed away. His past wife, Jo Kimball, can be contacted by:

phone- (813) 973-0996
fax- (813) 973-7002
e-mail- prodedi@discovery-experimental.com
writing-
James Kimball no longer can be written to. To get in contact with his family, you may use the specified e-mail address above.

Verified Declaration of James T. Kimball

This declaration contains the truth and the statements contained herein are true and correct to the best of James T. Kimball's ("KIMBALL") knowledge and belief. Additionally, under the penalty of perjury and willing to take a professionally administered truth serum or polygraph as to all statements contained herein; KIMBALL says the following:

1. Around 1990 KIMBALL formed Discovery Experimental and Development, Inc. (“DEDI”), a pharmaceutical research company to research and develop products to benefit mankind. KIMBALL additionally formed ASTAK, Inc., a dietary supplement research company along with initiating the forming of a non-profit organization, Global Health Information and Medical Research Institute, Inc. (“GHI/MRI”), in an effort to supply the public truthful information regarding any medical affliction, free of charge.

2. These corporations existed between the period of 1990-2000. Over the years, KIMBALL was the president of the aforestated companies and, as such, did not receive any salary or corporate issued bonuses. The majority of people, companies and universities that assisted DEDI and GHI/MRI did so to help develop products to help humanity and without payment for their services. The entities which became involved in this effort were doctors, scientists, universities and private corporations from around the world.

3. Over that ten year span, all companies KIMBALL was affiliated with, or president of, generated approximately three million dollars which amounts to $300,000 gross income per year. Three hundred thousand dollars per year might pay the salaries of three top scientists in the research field yet KIMBALL’s affiliated companies operating at a $300,000 yearly income paid employee salaries, and maintained a 6,000 square foot research facility in Wesley Chapel, Florida; a 2,000 square foot facility in Tijuana, Mexico; and offices in San Diego, California and Tampa, Florida. On site scientists at Wesley Chapel consisted of two over the years, while off site doctors and scientists assisting KIMBALL were at: Temple University; University of Southern California; University of South Florida; Florida State University; University of Toronto, Canada; the National Institute of Health; and a multitude of private research companies, doctors and scientists world-wide. The vast majority of scientists, doctors and such assisted KIMBALL’s companies in an effort to develop products to help mankind and did so from their hearts and received no remuneration at all for their services.

4. The first active ingredient DEDI developed was a liquid selegiline which, at its origin, is natural and extracted from a plant. Classified by scientists as a botanical, this product alone had the potential to improve everyone's quality of life. Notwithstanding addressing terminal diseases, enhancing the immune system and extending life dramatically. Over the years selegiline proved to do that and much more. Prior to 1991 no one in the world had been able to produce liquid selegiline in a pure form and stabilize it, nor to present date to KIMBALL’s knowledge.

5. The actions of properly made pure selegiline are well known by scientists, and very simple. Once in the blood stream, the product stimulates a tissue in the brain to produce another chemical naturally, which depletes as we age. In some people this brain tissue degenerates too quickly and people are afflicted with terminal neurological diseases such as Parkinson’s. This tissue is called the substantia nigra, which emits a chemical that retards the degeneration of brain cells and revives dying neurons, as test results proved. Without the substantia nigra emitting the chemical to sustain brain cell life, the life expectancy of human beings was estimated to be under 5 years. As people age the substantia nigra degenerates, the immune system drops, hormone levels drop, as do all other bodily functions, such as mobility and sex drive, due to the fact the brain cells are malfunctioning and dying due only to the lack of this chemical. The brain runs the body. If the brain is operating properly, the body normally functions properly.

6.Over a ten year period, DEDI’s selegiline product proved to be effective in treating Parkinson’s disease, Alzheimer’s disease, Multiple Sclerosis, nervous system disorders, pain, hormone depletion, high blood pressure, cancer and others. People using DEDI’s selegiline for general health, or quality of life, who had no medical problems consistently reported dramatic improvements in their quality of life to include increased memory, increased energy levels, increased sex drive, increased mobility and cognitive functions. Older people were driving again and getting out of wheel chairs. Over the years, life extension in animals revealed a dramatic increase, around a 50% increase. No serious side effects were reported in ten years of public use with DEDI’s product.

7. KIMBALL learned early on about the corruption within the pharmaceutical industry and the FDA. KIMBALL also learned from the top scientists and doctors around the world that, almost without exception, every active chemical ingredient within every dietary supplement and pharmaceutical drug differs by each manufacturer. Some are dramatically different even though the chemical name of their active ingredient is allowed to be called the same. That is why some generic drugs do not work and cause adverse side effects and sometimes death. However, some generic drugs are made better and purer than the original drugs introduced which work much better with less adverse side effects. The same with dietary supplements with allegedly the same active ingredients. The differences with dietary supplements derived from food, plants or a synthesized version is the side effects are normally negligible to none where drugs synthesized by other means produce serious side effects, including death. DEDI found producing an effective active ingredient requires exacting high purity standards. Those standards are not the standards of the FDA or the pharmaceutical industry. Their standards are all money related. FDA employees receive graft from pharmaceutical companies and have been caught on more than one occasion. Drug companies find it’s much cheaper to produce an impure active ingredient than a pure one, thus the impure drug is produced rather than a pure one. Many trials and test results on new drugs going through the FDA approval process are rigged and altered much too often. Not only do the American people pay exorbitant prices for these manipulated drugs, many pay with permanent disabling side effects, while others pay with their lives. And all the time, there are much better products out there to treat their afflictions which are suppressed by the pharmaceutical industry and the FDA. DEDI found working with the top scientists and researchers in the world that most of the products have been discovered that will treat or cure most all terminal diseases and afflictions, including dramatic life extension. However, that information is suppressed by the pharmaceutical industry, the FDA and some government officials.

8.The pharmaceutical industry blocks the information and development of these products because many of them are much cheaper and are far more effective with less side effects than the products they now have in the marketplace making billions of dollars. If these new, much more effective products, were allowed to get to the consumer; even one, would have the potential to eliminate the sale of 50 to 100 over-the-counter (“OTC”) and prescription (“RX”) drugs. That could easily cost the pharmaceutical companies, which are currently producing those products, hundreds of billions of dollars a year in income. The pharmaceutical industry controls the FDA, the federal government and state employees via Political Action Committees ("PACs") (lobbyists) and payoffs. So many people in the United States die or live a debilitating life with pain and suffering just so the pharmaceutical industry, in general, can continue to make billions of dollars.

9. KIMBALL spoke numerous times to Dana Barnett, the President of Somerset Pharmaceuticals, Inc. and Vice-President of Mylan Laboratories, Inc., about the issue of humanity, human rights, and the right to life, versus the almighty dollar. Around 1995, KIMBALL had met with Barnett in an attempt to persuade their pharmaceutical cartel to back off from their attempts to put DEDI out of business.

10. Somerset Pharmaceuticals, which is owned by Mylan Laboratories, Inc. and Watson Pharmaceuticals with affiliates such as Sandoz Pharmaceuticals, instigated the FDA and the State of Florida Dept. of Health (“DOH”) into a conspiracy that lasted 10 years and ended with DEDI out of business and KIMBALL in prison. Notwithstanding, their combined actions cost the lives and the quality of life of hundreds of thousands of Americans, if not millions. The people involved in this lethal conspiracy include, but are by no means limited to: Don Leggett, Dennis Degan, Agent Randy Matteson, Agent Chastony, Dr. Katz, Attorney Jennifer Bragg-Jones, all with the FDA; Jerry Hill, Agent Gregory Jones, Agent Deborah Orr and Attorney Robert Daniti, all with the DOH; Eleventh Circuit Court of Appeal Judge Charles A. Wilson; U.S. District Court Judge Richard A. Lazzara; U.S. Magistrate Judge McCoun; Assistant U.S. Attorney Michael Rubinstein; ex-FBI agent; and Bradley Vaughn, Probation Officer. The names of prominent conspirators were deleted from this public declaration to protect innocent people, however, the names are revealed in a confidential declaration being held by the trusted public.

11. Somerset Pharmaceuticals had acquired the rights and FDA approval for a product which contained an impure active ingredient called selegiline hydrochloride. This selegiline hydrochloride product was manufactured by a company in Budapest, Hungary and was shipped to the United States for redistribution by Somerset Pharmaceuticals. Somerset named this drug Eldepryl. The FDA “did not” approve Eldepryl to be a drug by itself. The FDA approved its use “only” to be used in combination with a dangerous prescription drug with serious side effects called Levodopa, and only for use in “one single disease” called Parkinson’s. KIMBALL’s companies were attempting to develop a different chemical entity that was similar, but much better than Somerset’s.

12. Heading up the trials, called Data-top, for Somerset was a man named Ira Shoulson. Dr. Shoulson oversaw the trials and testing of Somerset’s selegiline hydrochloride product. The testing of Somerset’s selegiline hydrochloride, which was made in Budapest, under the watchful eye and control of Dr. Shoulson were manipulated so they “would not” reveal an unknown contaminant which the University of Toronto found. DEDI’s head scientist believed he had identified the unknown contaminant as a neuro toxin. The FDA and the DOH were both advised about the contaminants in Eldepryl and they could care less. The government’s own records reveal the contaminants and the Somerset cover up, still they did nothing letting the compromised public who were dying of incurable Parkinson’s disease to further suffer and die with the use of Somerset’s product.

13. While KIMBALL’s companies were researching the methods to properly make selegiline, and prior to its development in the spring of 1991, Somerset, the FDA and DOH started their conspiracy. They earmarked DEDI’s premises and in 1990 they committed illegalities which lead to KIMBALL’s arrest. The case was thrown out due to their combined illegal acts.

14. In 1991, as soon as selegiline was developed, KIMBALL petitioned the FDA for an administrative determination asking the FDA to classify DEDI’s selegiline product in the food additive, vitamin class of product, i.e., dietary supplement, with medical claims. The FDA violated KIMBALL’s First Amendment right to petition, his Fifth Amendment right to due process, violated the laws which govern them, returned KIMBALL’s petition without administrative review.

15. Shortly after the development of selegiline, Somerset moved its headquarters from New Jersey to Tampa, Florida, 15 miles from DEDI and they remained there until KIMBALL was indicted and convicted in 2000, then moved away. After Somerset moved to Tampa, they hired private detectives to work with the DOH and federal agents in surveillancing DEDI and KIMBALL’s activities. The DOH and the federal government agents were sharing information with Somerset, which is illegal. The government conspirators even told Somerset not to file a civil suit against DEDI and KIMBALL until after the government and DOH had conducted their planned search, seizure and confiscations of DEDI, and KIMBALL’s residence, which was planned for May 12, 1993. The records and actual written communications between the U.S. Government employees and the representatives of Somerset Pharmaceuticals, and their attorneys, are on this website under the Conspiracy Page.

16. KIMBALL had surmised that Mylan Laboratories, who was one of the largest drug producers affiliated with Sandoz, had told their paper pharmaceutical company, Somerset, to move to Tampa to assist, influence and bribe any and all officials they could, to get rid of DEDI and KIMBALL.

17. Prior to the raid on May 12,1993, with the help of universities, doctors and scientists world-wide, DEDI developed products exceedingly effective in treating life threatening viruses, bacterial infections and fungi infections. Additionally, DEDI had a product in process that was an extract from a mushroom which had been proven to enhance the immune system so high it had the ability to treat and cure skin cancer. KIMBALL had collaborated with Japanese scientists on the project and at the same time DEDI had acquired another extract from Europe which scientists had told KIMBALL worked effectively to treat liver cancer which is deemed deadly and untreatable in the United States. The DOH conspirators illegally confiscated those research products on May 12, 1993 and never returned them.

18. With the help of a renowned scientist from the National Institute of Health (“NIH”), Dr. Willie Burgdorfer, and the use of the NIH’s sophisticated equipment, a unique form of a mineral was developed by DEDI. Once later perfected, this specifically engineered mineral was encircled by a protein which proved to be lethal against all viruses, bacteria and fungi tested against it, to include full blown AIDS. Without the direct assistance of Dr. Willie Burgdorfer from the Rocky Mountain division of the NIH, the specific engineered mineral would never have been developed to its highest potency. The original version of this mineral product, along with the perfected version under the NIH, has never been produced by anyone to date. Over the years with all the testing and human trials conducted, this single product, and versions of it produced by DEDI, revealed staggering results. The testing, trials and human use of varying potencies of DEDI’s mineral product had not only revealed its lethal powers by killing the AIDS virus, it additionally inhibited or killed the spirochetes in Lyme disease, viruses and bacteria attributed to Hepatitis C, along with staph infections. It was effective in treating flesh eating staph. It was reported by one doctor using the product in patients at the final stages of leukemia that it normalized the white/red blood cells. Leukemia symptoms disappeared, meaning the leukemia wasn’t a cancer at all, it was caused by some unknown virus. Another doctor reported it had been effective in some of his patients afflicted with Alzheimer ’ s disease reflecting that at least some forms of Alzheimer’s are viral or bacterial related. Tests revealed it killed the staph bacteria known as staphylococcus aureus, which are staph infections that are resistant to known antibiotics. These resistant strains of bacteria are also known as MRSA. In less potent forms, DEDI’s mineral product was exceedingly effective in treating sinus infections, ear infections in children, gum infections, fungi infections under the nail in rapid order. Usually in one day of administration. Taken daily, the product appeared to help prevent colds and viral infections; however, it was not immediately effective with regard to a common cold.

19. It was not until much later that a scientist researching the results of the product finally determined how and why the product worked when common sense science suggests it shouldn’t. Scientists concluded that viruses and bacteria could not mutate to become resistant to it because it was a mineral. They concluded that the body would have to change in order for the product not to work. Toxicity tests conducted at the University of Toronto revealed that DEDI’s mineral product had no toxicity whatsoever, even at over 1,000 times the normal dosage.

20. Even though the product is a mineral and most assuredly a dietary supplement, KIMBALL believed that certain potencies of the product to be used for serious infectious diseases should be listed as an over-the-counter (“OTC”) drug. KIMBALL sent in some of the trials and their results to the FDA, and asked them to approve the labeling, and list certain versions of this product as an over-the-counter drug. In 1998 the FDA agreed to do so and listed one version OTC with approved labeling stating “To be used for general internal infections.” At the time, there was no question whatsoever that once the general public found out about DEDI’s product, tried it, and saw for themselves how effective it was, it had the potential to eliminate hundreds of OTC and RX drugs from the shelves. The pharmaceutical industry immediately blackballed the distribution of KIMBALL’s product by threatening the pharmaceutical distributors if they distribute DEDI’s product it would be the last product they ever distributed. DEDI did not have the money to promote and distribute the mineral product.