Friday, January 15, 2010

The cancer conspiracy is led by the FDA-NCI-AMA-ACS hierarchy.

"" The Food and Drug Administration (FDA) is a government agnecy whose supposed job is to "protect" the public from dangerous drugs, foods, medicines, toxins, and medical procedures. In fact, the FDA is a gestapo-type organization only serving the interests of the major drug companies and medical establishment.

The various senior members of the FDA rotate lucrative positions on the boards of major drug companies and other key organizations. Members of the FDA have been found to have severe conflicts of interest, often owning stocks in the very companies they are supposed to to "monitoring, policing and controlling".

This is not some paranoid conspiracy delusion. This is exactly what they do. They protect the interests of the drug companies by 1) ensuring important drugs get swift approval despite dangers or ineffectiveness, and 2) monitor and act to eradicate threatening competition from alternative or "non-team player" individuals and organizations. ""

"People think the FDA is protecting them - it isn't. What the FDA is doing and what people think it's doing are as different as night and day." - Herbert L. Ley, Jr., M. D., former Commissioner of the FDA ..

"The hearings have revealed police state tactics . . . possibly perjured testimony to gain a conviction . . . intimidation and gross disregard for Constitutional Rights." - Senator Edward Long, U.S. Senate hearings on the FDA

The cancer conspiracy is led by the FDA-NCI-AMA-ACS hierarchy. The initials stand for the Food and Drug Administration (FDA), the National Cancer Institute (NCI), the American Medical Association (AMA), and the American Cancer Society (ACS).

The cancer conspiracy also includes the large pharmaceutical companies and key research centers such as the Memorial Sloan-Kettering Cancer Center in New York City and selected university research labs.

The key personnel move in and out of official positions within these organizations, sit on common boards or investigation committees, and have both formal and informal networks.

When a researcher or alternative medicine advocate is identified as a threat to the power or even the official views put out by the ruling hierarchy, the maverick is placed on various published and unpublished blacklists. Funding is stopped, legal harassment often begins, public denunciation as a quack frequently follows, and if the outsider persists in offering or advocating a non sanctioned treatment, then rougher, clandestine methods can be employed.

It would take thousands of pages to describe various individuals who have fought the cancer conspiracy and how their threat to the ruling powers was neutralized. These pages can only summarize some of the more famous cases and facts which reveal how the cancer conspiracy functions, but those who wish to know more can pursue the details on their own, using the names and references offered here as a starting point. The people and procedures described in these pages are by no means inclusive, only the most notable or most promising.

The FDA (Food and Drug Administration) is the government police force which approves experimental studies for those it favors and hinders approval for those it dislikes.

It conducts semi-legal break-ins (constitutional procedures are often ignored), confiscates records so that critical documentation is often lost or at least unavailable for months and years, and at times has interfered with constitutional protections through conspiratorial relationships with private organizations who share the same suppressive goals.

New medical breakthroughs that threaten the sanctioned and financially lucrative treatments are ignored or "studied" for years. The FDA thus frequently subverts its legislated purpose which is to promote and protect the public health. Having lived in Washington, D.C., I know that the FDA is regarded by many astute civil servants as the federal agency with the lowest morale. A dark cloud of oppressive inertia, corruption and bureaucratic sloth pervades its corridors.

Dr. J. Richard Crout, test director at the FDA Bureau of Drugs beginning in 1971, described the agency's agony in Congressional testimony on April 19, 1976 as follows:

"There was open drunkenness by several employees which went on for months ... crippled by what some people called the worst personnel in government. There was intimidation internally by people . . . People, I'm talking about division directors and their staff, would engage in a kind of behavior that invited . . . insubordination - people tittering in comers, throwing spitballs; I am describing physicians, people who would . . . slouch down in a chair, not respond to questions, moan and groan with sweeping gestures, a kind of behavior I have not seen in any other institution as a grown man . . .

Prior to 1974, not one scientific officer in our place knew his work assignments, nor did any manager know the work assignment of the people under him."
In 1967, FDA stopped the use of an experimental cancer vaccine which was producing significant results.

It was developed by H. James Rand, inventor of the heart defibrillator. J. Ernest Ayre, an internationally recognized cancer specialist (co-developer of the PAP test) and Dr. Norbert Czajkowski of Detroit, Michigan assisted Rand. Treating only terminal cancer patients, the Rand vaccine produced objective improvement in 35% of 600 patients while another 30% demonstrated subjective improvement. "One 65 year old woman with spreading tumor" was "completely cured in 4 months."

Another woman with extensive breast cancer was cured in 6 months. The FDA stopped the vaccine's use in a federal court hearing where neither the cancer patients nor their doctors were allowed to testify. When U.S. Senator Stephen Young of Ohio protested, it was to no avail. Senator Young could get nowhere with FDA Commissioner James L. Goddard. Senator Young recalled:

"I could not move them. They would not even agree to a modification of the ruling (banning the Rand vaccine), which would at least allow the 100 (cancer) patients at Richmond Heights (Ohio) to complete their injections. The Justice Department was prepared to go along, but the FDA Commissioner, Dr. James Goddard, was adamant, even belligerent. It's wrong of the government to snatch away this hope when there is no evidence against its use offered in court. It's damnably wrong."

It is known that when FDA Commissioner Goddard's own wife had serious health problems and orthodox medicine could not help her, Goddard contacted alternative health practitioners who quietly healed his wife. But for the suffering victims of cancer who needed the Rand vaccine or some other nontraditional treatment, Goddard lowered the boom, using the federal courts to enforce his dictum. Such are the ways of the FDA.

Goddard's greatest disservice to the American people was his persecution of DMSO, a simple molecule which often brought miraculous pain relief and offered numerous possibilities for medical advancement in other areas, including cancer.

One respected science writer suggested that Goddard crushed DMSO research in order to gain increased police powers from Congress. The FDA has never admitted its errors regarding DMSO although the positive studies from qualified scientists number over a thousand while the FDA's criticisms have been shown to be almost completely based on lies or unsubstantiated rumors. Yet by the late 1980s, twenty years later, the FDA continues to imprison DMSO advocates.

The malignity of Goddard's arbitrary and conscienceless acts in 1966-1968 against reputable scientists, dedicated doctors and the public good is one of the darkest chapters of FDA history.

No one is sure of the real reasons why it happened and why it continues to be covered up twenty years later. It has been suggested that one or more drug companies sabotaged DMSO because it threatened so many of their profitable products. One drug company executive reportedly told the leading DMSO researcher:

"I don't care if it is the major drug of our century - and we all know it is - it isn't worth it to us."
Who had the power to keep such a miraculous drug off the shelves? Surely not just an FDA Commissioner flexing his muscle. Was it a combination of drug companies whose individual profits were threatened by the miracle drug's possibilities?

"(It is) not our (FDA) policy to jeopardize the financial interests of the pharmaceutical companies." - from testimony before Congress of Dr. Charles C. Edwards, at the time Commissioner of the FDA It has also been surmised that FDA Commissioner Goddard used DMSO in 1966 in an attempt to become the medical dictator of America. In the years that followed, FDA officials simply refused to expose the agency's "dirty laundry." Hence the on-going suppression of what many recognize as "the major drug of the century. " "

Full Article and More on FDA Suppression
FDA Reign of Terror