Friday, December 7, 2012

Where chemtrails come from

The History of Biological Weaponization

Vance Ferrel

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BEGINNINGS

How it began. The Soviet germ weapon program began in the 1920s and

gradually grew into a mammoth operation. The objective was to develop

weapons capable of infecting people with anthrax, typhus, and other diseases.

Stalin spent large amounts of money on the project.

We get involved. Back then, the United States had no germ weapons. By

the late 1930s, with intelligence agencies warning that Tokyo and Berlin

had biological weapons, Washington began to mobilize against germ attacks

in 1942. President Franklin D. Roosevelt publicly denounced the

germ warfare plans of the enemy, even while preparing to retaliate with

similar ones. George W. Merck, president of the drug company, Merck &

Co., was placed in charge of the new project.

Fort Detrick. The army base at Fort Detrick, Maryland, was selected as

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The 1960s

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the place where the research should begin. It would eventually become an

immense U.S. biological weapons center.

When World War II ended. Meanwhile, in 1946 at Sverdlovsk, the Soviets

set up a factory that specialized in anthrax. The next year, outside

Zagorsk, they built a complex for making weapons out of viruses, including

smallpox.

The outbreak of the Cold War and the Korean War in 1951 led Washington

to put new emphasis on planning for germ battles, and rapid expansion

of facilities took place at Fort Detrick. Nuclear testing was already

occurring both in the Soviet Union and the United States.

Spraying San Francisco. In one experiment, U.S. scientists sprayed mild

germs (Sarratia marcescens) on San Francisco, to assess the ability of pathogens

to spread through urban centers. The germs were meant to be harmless.

However, they were not harmless enough. Eleven patients were admitted

to Standard University Hospital with sarratia infection. One patient,

Edward J. Nevin, died. The physicians were so astonished at the outbreak

of a totally rare disease that they wrote it up in a medical journal. Years

later, in 1981, the government denied any responsibility and the judge

dismissed a lawsuit (Cole, Clouds of Secrecy, pp. 52-54, 75-104).

Clusters of anthrax. Another U.S. project consisted of cluster bombs,

each of which held 536 bomblets. Upon hitting the ground, each bomblet

would emit a little more than an ounce of anthrax mist. This terrible disease,

if untreated, kills nearly every infected person (a very high mortality

rate, even compared with the Bubonic Plague and most other pathogens).

Practice runs. A substance, something like anthrax, was used in practice

sessions against St. Louis, Minneapolis, and Winnipeg, cities whose

climates and sizes were considered similar to Kiev, Leningrad, and Moscow.

Code named Project Saint Jo, the clandestine tests involved 173

releases of noninfectious aerosols (CBW Conventions Bulletin, June 2000,

pp. 16-19).

In 1956, the Soviet defense minister, Georgi Zhukov, told a Communist

Party Congress that any modern war would certainly include the use of

biological weapons (Sidell et al., Medical Aspects, p. 54). When American

intelligence learned of that statement, it energized our bioweapons program

even more.

The same year, American U-2 spy planes began flying over the Soviet

Union. By that time, the Russians had built many secret bases throughout

the nation, which were developing and producing germ weapons.

Island in the Aral Sea. Shortly afterward, an American U-2 spy plane,

flying high over a desolate island in the Aral Sea, photographed dense

clusters of buildings and odd geometric grids which CIA agents recognized

as belonging to a biological weapons base (Mayday: Eisenhower, Khrushchev

and the U-2 Affair, p. 121).

The bull’s eye ring pattern was identical to one at our Utah desert

biological testing base, where roads, sensors, electrical poles, and test subjects

were placed at increasing distances from germ sprayers.

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The 1970s

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Germ factories. By the late 1950s, the U.S. was building factories capable

of producing enough pathogens and biological toxins to fight wars.

But, officially, they were only doing that which was needed to defend against

such attacks.

Q fever. In 1956, the Pine Bluff Arsenal, an army base in the woods of

northern Arkansas, was turned into a weapons factory producing bacteria,

including tularemia. Soon it expanded into virus production. Before long,

it was also producing Q fever (Sidell, et al., Medical Aspects, pp. 50-51,

429).

Q fever is a relatively mild disease which was meant, not to kill enemy

troops, but cripple them with chills, coughing, headaches, hallucinations,

and fevers of up to 104o F. It was thought that sick soldiers would cause

more problems to the enemy in a war than dead ones. Another virus was

Venezuelan equine encephalitis (VEE), a horrible disease.

THE 1960s

Nixon was absent. President Eisenhower was briefed on Fort Detrick’s

advances just before he left the White House. The full meeting of the National

Security Council occurred on February 18, 1960. But Richard Nixon,

the vice president, was absent. He was preparing for his run for president.

By this time, researchers had found ways to concentrate the diseases and

extend their storage lives from one to three years.

Under Kennedy. Spending on biological weapons greatly increased after

John F. Kennedy took office in January 1961. The new secretary of defense,

Robert McNamara, along with the Joint Chiefs of Staff thoroughly

analyzed the program and were satisfied that the new weapons would prove

very handy in case of war, especially those (such as Q fever) which could

cripple the enemy’s troops rather than kill them. Caring for injured soldiers

would cause more problems than disposing of dead ones. The development

of virus weapons was accelerated (Regis, Biology of Doom, pp.

185-186).

Tests were made in both the Pacific and Alaska. The hundreds of personnel

involved in these tests were coordinated from Fort Douglas, near

Salt Lake City.

Improving smallpox. As we became more involved in the Vietnam War,

work focused on improving smallpox and its delivery. This ancient disease

was highly contagious, and killed about a third of its victims, mainly from

blood loss, cardiovascular collapse, and secondary infections as pustules

spread over the body (New York Times, June 15, 1999).

It was during this time that biologists at Fort Detrick learned how to

extend the life of the variola (smallpox) virus by refrigerating it in a special

way which made use of freeze drying. In connection with this, an ominous

discovery was made: Freeze drying would kill some microbes, but not smallpox

(Hahon, Screening Studies, pp. 15, 55). This meant they could be

stored for an indefinite period of time. Methods were devised for making it

into a fine powder and spraying it.

Another fake test. In May 1965, Fort Detrick scientists packed fake

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The 1980s

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smallpox powder in suitcases and sprayed it in Washington National (now

Reagan International) Airport, just across the Potomac from the Capital.

The resultant report concluded that one in every twelve travelers would

have become infected, quickly spreading the disease throughout the nation,

and that smallpox powder would be an excellent choice for terrorism

against a foreign power.

A special warfare advantage is that its incubation period is a full twelve

days before the first symptoms (malaise, headache, fever, and vomiting)

begin to occur and medical diagnosis is made.

Our military leaders considered applying smallpox to the Ho Chi Minh

Trail in Vietnam. But the anger caused by a fearful spread of the disease

throughout southern Asia, and the quick retaliation likely to come from

Chinese and Soviet stockpiles, were feared. So the project was abandoned.

Protests begin. Nearly all of the information you have just read was not

generally known back then (nor is much of it known today). Nevertheless,

by the late 1960s, the American public had gradually become aware that

biological weapons were being made at Fort Detrick. Crowds of Vietnam

anti-war protesters gathered at its entrance. Books opposed to germ warfare

began being published (Susan Wright, ed., Preventing a Biological

Arms Race; S.M. Hersh, America’s Hidden Arsenal; etc.).

Nixon calls an end. Then, on November 25, 1969, Richard Nixon announced

the end of biological weapon testing. In January, Nixon also stopped

all our chemical weapons programs. The scientists were told to focus their

work on “germ defense,” not germ attack.

But no limits were set on the quantities of dangerous microbes or chemicals

which could be used in that research. So our stockpiles were not

reduced.

Overseas: business as usual. But our biological/chemical defense program

had been greatly damaged. Our scientists were-well aware of the fact

that it takes 18 months to develop a weapons-grade agent and ten years to

develop a good vaccine against it. They also knew that the Soviet Union

would not stop their deadly projects, just because we had.

By that time, China was also working on chemical and biological

weaponization projects. Soon after, certain Near Eastern nations would

begin doing the same.

THE 1970s

The Senate is angry. In the fall of 1975, Senate hearings uncovered a

number of astonishing projects, plans, and plots by our BW (biological

warfare) scientists, working with the military.

At least 16 different, terrible diseases were stockpiled, mostly at Fort

Detrick. The single largest item was anthrax.

The germ treaty. That same year, 1975, an international germ treaty

took effect. All BW arsenals throughout the world were to be totally destroyed

within three years. How wonderful if that had happened! But it

did not take place.

Soviets in fast forward. Shortly afterward, secret papers smuggled out

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of the Soviet Union revealed that Soviet leaders were continuing to amass

and develop germ weapons. Then, in 1978, a senior Soviet diplomat at the

UN defected to the United States (Arkady Shevchenko, Breaking with Moscow,

pp. 34, 172-174, 179, 202). But his warnings, like those in the secret

papers, were largely ignored by our leaders. They did not believe him.

The Sverdlovsk accident. Then, in October 1979, a Russian-language

newspaper for Russian immigrants living Germany revealed something important.

Newly arrived immigrants told of a thousand Russians living in a

village close to Sverdlovsk, an industrial complex in the Ural Mountains,

who had, within two weeks, died of anthrax. The report said that Soviet

troops quickly entered the area and spread fresh dirt over the ground (Jeff

Goldberg, Plague Wars, pp. 71-74).

This story went around the world. U.S. intelligence compared data and

photos and verified activity in that area at the time specified. It was clear

that an accident had occurred and the Soviets were, indeed, continuing to

produce, refine, and stockpile biological weapons.

Deadly anthrax. The anthrax bacillus can enter the human body in three

ways: into the lungs by breathing spores, into the digestive tract by eating

infected livestock, or into scrapes or open sores on the skin.

Bacteria from spores in the lungs produce several toxins that attack

cells. The first symptoms are coughing and fatigue, then a brief recovery as

the body fights the infection. This is usually followed by respiratory failure

and death. But a major drawback in attacking an enemy with anthrax is

that the spores can persist in the soil for decades.

THE 1980s

Reagan approves. In January 1981, Ronald Reagan took office; and,

soon after, some of his researchers gathered evidence that the Soviet Union

was working on a two-track plan: Stockpile old-fashioned germ weapons,

such as anthrax, while developing advanced, bioengineered pathogens.

A research paper, issued by the army’s Drugway center in Utah, warned

that such highly developed germs could be used to make highly concentrated

weapons. In fact, genetic manipulation could change such diseases

as anthrax, so they could not be treated by any medicine or protected

against by vaccines.

In early 1984, Reagan ordered more money given to the military and

intelligence to assess what was happening in certain foreign nations. In

April, his administration told the public of the danger. Shortly afterward,

the Wall Street Journal began a series of seven articles, warning about the

dangers of super-germ weapons (Wall Street Journal, April 23, 1984, et

al.).

More congressional hearings followed. America was awakening to the

danger. Under Reagan, all types of new military weapons were produced.

Biodefense alone was given $91 million annually. We started inventing our

own “super bugs.”

In the name of defense. By this time, our leaders were declaring that we

had not violated the earlier biological weapons treaty, since all research

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The 1990s

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was only done for purposes of defense. This “biological defense” research

between 1980 and 1986 produced 51 projects which produced strange,

new bacteria and viruses; 32 which increased toxin production; 23 which

no vaccine could resist; 14 which could not be diagnosed; and 3 which no

drug could treat.

Urgent call for vaccine. In December 1984, a paper was produced by

Fort Detrick researchers, which urgently called for the stockpiling of large

amounts of anthrax and botulinum vaccine to inoculate two million soldiers

against attack.

By 1985, the army asked the nation’s pharmaceutical manufacturers to

develop an improved anthrax vaccine, since the only one available frequently

caused a variety of negative effects, some of them long-term. To

add to the problem, that vaccine did not protect against all types of anthrax.

Brain-damaged children. But no drug company wanted to sign a contract.

A rising number of lawsuits had been hitting the courts. Parents

were suing the pharmaceutical companies because of vaccines which had

caused brain damage and death to their children. Many immense judgments

had been awarded by sympathetic juries.

The Michigan plant. So the army turned to the only licensed manufacturer

of anthrax in America, a decades-old facility with run-down buildings

and equipment owned by the Michigan Department of Public Health.

Brushing aside concerns, on September 29, 1988, the army signed its

first-ever contract to purchase large quantities of anthrax vaccine. The

initial order was for 300,000 doses. The army bought the equipment and

gave Michigan five years (till September 1993) to deliver them.

Iraq also doing it. A few months earlier, in June, it was learned that

Iraq, under Saddam Hussein’s leadership, was beginning to build its own

biological weapons stockpile. By that date, intelligence reports disclosed

that Baghdad had already used Clostridium botulinum (botulism mold) to

make a deadly toxin said to be 10,000 times more lethal than nerve gas.

Iraq was said to be working on large quantities of anthrax and other biological

agents. Reports had even disclosed that Saddam Hussein had scientists

preparing things useful for assassination of selected individuals, and

that his son-in-law, Hussein Kamel, was personally in charge of the research

work.

Made in the U.S.A. But that was not all: U.S. intelligence revealed that

the Iraqis were buying their starter germs—from an American company,

the American Type Culture Collection (ATCC). Without such starter germs,

Saddam’s germ warfare development program could not go forward. We

provided what was needed for him to get started in business (Defense

Intelligence Agency, report dated June 28, 1988).

The ATCC, at that time located in Maryland on the outskirts of Washington,

D.C., housed the world’s largest collection of germ strains, including

the especially virulent variants of anthrax and botulinum which our

germ warfare experts had developed in the 1950s.

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The ATCC sold from its stockpile to overseas nations, so their scientists

could find ways to improve the health of their citizens. At least, that was

the plan. Licenses to purchase the most virulent strains could easily be

obtained from the Department of Commerce.

The first purchase had been made in May 1986, when ATCC sold an

assortment of terrible disease germs to the University of Baghdad (ATCC

batch No. 010072; date of shipment: May 2, 1986). Included among them

were three different types of anthrax, five of botulinum, and three of brucella

(which causes brucellosis, an incapacitating livestock disease).

However, U.S. officials expressed little concern. Iraq was considered a

friendly power in its fight against Iran, which earlier had held U.S. hostages.

They even seemed not to be disturbed when Iraq used nerve gas on

Kurds in northern Iraq. No calls were placed to ATCC, notifying them to

stop selling to Iraq—or anyone else.

Three months after the intelligence report had been submitted to U.S.

government leaders, a second large shipment of germs was sent to Iraq on

September 29, 1988. It included four types of anthrax, including strain

11966, a type of specially deadly anthrax developed by Fort Detrick in

1951 for germ warfare.

The order was placed by the Iraqi Ministry of Trade’s Technical and

Scientific Materials Import Division (TSMID). Even though we had earlier

identified TSMID as a front for Baghdad’s germ warfare program, the State

Department permitted the shipment to be sent.

Closing the barn door. It was not until February 23, 1989, that the

Commerce Department banned sales of anthrax and dozens of other pathogens

to Iraq, Iran, Libya, and Syria (all of which had earlier been able to

buy virulent germs from ATCC). By that time, it was too late.

Drug-resistant germs. It was becoming obvious that microbes were becoming

increasingly resistant to antibiotics and other medicinal drugs.

This included drug-resistant tuberculosis, new varieties of E. coli, and

AIDs. Other diseases were becoming harder to treat. How would we deal

with drug-resistant germs sent to us by foreign powers?

Funding refused. Throughout 1989 and the next year, an effort was

made to obtain government funding for defenses against this threat. But

the General Accounting Office said the project requests, totaling $47 million

including toxic germ items, did not involve “valid threats” (GAO, special

report, December 1990, p. 2). Senator John Glenn agreed and helped

quash efforts to obtain the funding.

Big news. By 1989, the Soviets were still considered a problem, yet it

was thought that they had shut down their germ weapon projects. But, in

October, a leading Soviet biologist (Vladimir Pasachnik) defected to Britain.

He had been the director of the Institute for Ultra-Pure Biological

Preparations in Leningrad, one of many research and development sites.

Pasachnik revealed that over 10,000 Soviet scientists were hard at work

on projects to produce both the worst possible kind of microbes and ways

to best deliver them to the enemy. Long-range missiles had been constructed

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which could carry them great distances. Cruise missiles were able to fly low

and spray them in the air.

For the first time, our leaders had the opportunity to actually learn

what was happening in the Soviet GW (germ warfare) program.

The Soviets had even perfected a type of bubonic plague which could

not be defended against or treated. Pasachnik disclosed that they had packed

a dry powdered form of the disease into bombs, rocket warheads, and

artillery shells. Yet this was only one of many Soviet germ warfare projects.

Investigators found that Pasachnik was able to provide detailed information

and freely admitted when he did not know the answer to a question.

Yet, in spite of this, U.S. leaders hesitated. Was Pasachnik really telling

the truth? Once again, nothing was done.

THE 1990s

Awakened by the Gulf War. By June 1990, our intelligence was focusing

on Al Tuwaitha, near Baghdad, and suspecting that it was an important

germ warfare production facility.

Then, on August 2, Saddam’s army invaded Kuwait. It was obvious that

we had waited too long. Hussein had biological warfare capability, and our

defenses were inadequate. We lacked detection devices for airborne anthrax

spores; they would not be developed by the January 15, 1991, deadline

that was set by the UN for Iraq’s withdrawal from Kuwait. There was

also little likelihood of having enough vaccine by that time. The antiquated

Michigan anthrax vaccine facility was not able to produce enough.

Warning our ships. On August 6, the U.S. Navy sent its commanders a

warning, that Iraq might have germ weapons which could be used against

ships 25 miles away or closer. “The Iraqis would deploy these agents if

needed” (Navy Operational Intelligence Center Report No. 0604327, August

6, 1990).

Already stockpiled. Two days later, another intelligence report noted

that Saddam already had “substantial amounts of botulinum toxin” which

was “probably weaponized.” Other germs being developed, or already available

for weaponization, included cholera, anthrax, staphylococcus enterotoxin

(SEB), and clostridium perfringens. “It is assessed that Iraqi forces

will use BW [biological weapons] only as a last resort” (Armed Forces Medical

Intelligence Center, Special Weekly Wire, 32-90(C)(U), August 8, 1990).

Anthrax shots begin. On December 17, Colin Powell recommended to

Secretary of Defense Dick Cheney, that inoculations should begin right

away. President G.H.W. Bush approved it. The army began urging the FDA

to permit it to give the botulinum vaccine to U.S. soldiers without obtaining

the “informed consent” normally required of patients given experimental,

unapproved drugs. The FDA reluctantly gave permission. That decision

laid the seeds of grief for many Americans in coming years.

The Pentagon gave anthrax shots to 150,000 Persian Gulf soldiers, many

of whom later developed the mysterious “Gulf War Syndrome.”

Another question concerned what to do with the remains of U.S. soldiers

killed by a germ attack. In response, a memo from Fort Detrick said

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that the remains would have to be soaked in a powerful chlorine bleach.

Only then could they be safely sent to the States for burial.

At the war’s end. After repeated bombings and 100 hours of action, the

sudden end of the Gulf War meant that Saddam did not have to release his

germs.

But it was discovered later that many of our “smart” bombs had not hit

their targets—and Iraq’s germ warfare plants, which were bigger and more

in number than we had earlier suspected, were largely intact.

Russians still busy. Vladimir Pasachnik’s disclosures turned out to be

correct. By January 1991, we had far more evidence that Russia had an

immense germ warfare program. But Russian leadership continued to deny

that it was producing biological weapons.

Inspections begin. On August 2, 1991, the first team of United Nations

Special Commission (UNSCOM) inspectors had arrived in Baghdad. UNSCOM

spent four years and repeated trips trying, in vain, to actually see what CIA

intelligence had discovered by the fall of 1991.

Alibek defects. In the autumn of 1992, Kanatjan Alibekov (who later

changed his name to Ken Alibek) defected from Russia and arrived in

America. He was debriefed for over a year. Alibek had worked in Soviet

germ warfare plants for 17 years and had risen to become the second in

command of Biopreparat, which U.S. intelligence had been tracking for

years. Biopreparat was the central agency in charge of all chemical/biological

weaponization production throughout Russia.

Alibek told the Americans that Russia had secretly produced hundreds

of tons of anthrax, smallpox, and plague germs for use against the United

States and its allies. Tens of thousands of people were employed at over 40

sites, spread across Russia and Kazakhstan.

He also told the techniques used to accomplish this, including breakthrough

methods devised after the U.S. stopped its own germ program in

1969.

First Trade Center bomb. Thirty-five days after Bill Clinton took office,

a bomb exploded in the basement of the World Trade Center. Among the

results of this wake-up call was renewed interest in developing and stockpiling

vaccines against biological weapons.

Iraq hard at work. Meanwhile, Iraq was rapidly improving its own germmaking

facilities. An Iraqi clerk told the UNSCOM team that Iraq’s large

Technical and Scientific Materials Import Division (TSMID) was actually

part of their intelligence services. By the mid-1990s, British and German

firms had sold nearly 40 tons of microbial food (needed to mass produce

germs) to TSMID. Iraq had purchased far more than it needed for normal

research and medical treatment. Yet as early as the late 1980s, the CIA had

already identified the true role of TSMID.

South African stockpile. By the mid-1990s, both Iraq and Libya were

trying to buy germs from South Africa. The Apartheid regime in South

Africa had, for years, been developing a stockpile of anthrax, botulinum

toxin, ebola, Marburg, and HIV virus (the cause of AIDS), to use against an

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uprising of blacks.

When the government suddenly collapsed in 1994, Libyan leader,

Muammar Qadaffi, sent agents to purchase supplies and hire out-of-work

scientists. They especially wanted Wouter Basson, who had been in charge

of South Africa’s former germ warfare program.

Tokyo attack. On March 19, 1995, a nerve gas attack was carried out in

a Tokyo subway, using sarin, which sickened thousands of people. Eventually,

the leaders of Aum Shinrikyo were jailed. It was later learned that the

cult had acquired some of its materials from ATCC, that Maryland germ

center, as well as from Russia.

Oklahoma bombing. One month later, on April 19, the Alfred P. Murrah

Federal Building in Oklahoma City was bombed. Nearly two hundred people

died. Although no chemical or germ weapons were used, it was also a

terrorist attack, the largest ever to occur in the U.S. up to that time.

First time inside a Russian germ facility. Stepnogorsk is a place you may

never have heard about. It is a city in Kazakhstan which had been built in

1982 as part of the Scientific Experimental and Production Base (SEPE).

This was the most advanced of all Soviet germ warfare plants, and the only

one on the edges of Russia. When Kazakhstan broke away from Moscow in

1991, its leaders wanted closer relations with America, and let them examine

the now-empty production facilities.

Andy Weber, a young diplomat stationed at the American embassy in

Kazakhstan, led the inspection team. Inside just one structure, Building

221, they saw ten 20-ton fermentation vats, each four stories tall. Each

one could hold 20,000 liters of fluid. The building was as long as two

football fields. Yet it was only one of more than 50 buildings.

Building 221, alone, could produce 300 tons of anthrax in just 220

days, enough to fill many ICBMs.

Yet the Stepnogorsk complex was just one of at least six Soviet production

facilities.

Immense production. American intelligence was beginning to realize

the astounding fact of what had been accomplished. Begun in 1973, by the

late 1980s, the Soviet germ warfare program had employed over 60,000

people, run by the military with an annual budget of close to $1 billion;

they had stockpiled immense amounts of plague, smallpox, anthrax, and

other agents for intercontinental ballistic missiles and bombers.

Two questions. But there were two questions: First, what had happened

to all that germ stockpile?

Second, where were the hundreds of scientists and technicians who

had once worked here? At its peak, Stepnogorsk alone had 700 scientists

and top-level technicians. Now there were only 180. Where were the rest?

Were they driving taxis or farming or had they been hired by foreign nations?

Fortunately, young Weber was fluent in Russian, and he set to work to

find answers. He had abundant opportunities, for the U.S. government

found he was very effective at obtaining uranium transfers to the U.S. It

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was Weber who first learned of the existence of Stepnogorsk, during a

hunting trip with a friend who was a high-placed Kazakh official.

Vector. Then there was Vector. The defector, Alibek, had earlier identified

this remote location in western Siberia as the Soviet’s largest and most

sophisticated virus facility. Russia had secretly moved its smallpox samples

there from Moscow, in violation of a 1992 treaty. That treaty broke down in

1995, when the Russians refused to permit the Americans to visit Vector

and other facilities. Obviously, they were still being used to store and work

on germ weapons. It would not be till several years later that we would be

able to enter that facility.

Scientists for hire. One evening during supper, Gennady Lepyoshkin, a

former Soviet colonel who had managed the Stepnogorsk plant after Ahibek

transferred to Moscow in late 1987, told Weber that Iran had repeatedly

tried to recruit remaining scientists and technicians at Stepnogorsk. But,

so far, they had not succeeded. But this could not continue forever. Everyone

at Stepnogorsk was impoverished; some were close to starvation.

Lepyoshkin asked for U.S. help to retrain these scientists at something

they could use to support themselves. Later, Weber relayed the message.

But, for a time, little was done.

The Aral Sea site. Lepyoshkin offered to show Weber other secret germ

sites in Kazakhstan. Especially important to the Americans would be a visit

to Vozrozhdeniye Island, located 850 miles east of Moscow, and the Soviet

Union’s largest open-air testing site. Located on an island in the midst of

the shrinking Aral Sea, it had been used to test brucellosis, Q fever, plague,

glanders, tularemia, and even smallpox. (“Vozrozhdeniye” means “Renaissance”

or “new life” in Russian.)

Buried treasure. After arriving there, Lepyoshkin told his new friend,

Andy Weber, a very deep secret: When the Soviets lost Kazakhstan, they

put their cache of anthrax into 66 stainless steel canisters, shipped them

on a train with 24 cars, poured bleach into the canisters, then buried them

under three to five feet of sand on this desolate island.

This discovery enabled the Americans to later dig up some of that anthrax,

test it, discover that part of it was still alive, and learn its potency.

There was enough buried anthrax to kill, many times over, every person in

the world.

Waiting to be dug up. But, when others learned the secret (now rather

well-known or I would not be mentioning it here), they could come to the

lonely, totally deserted island and dig up some of the anthrax canisters (so

many that they originally filled 24 box cars) and carry them back home!

One does not even need a boat to go there, for at certain times of the year a

sandbar extends out to the island.

Thousands of gallons. Meanwhile, UNSCOM inspectors in Iraq were trying

to learn the facts. On the evening of July 1, 1995, one of the Iraqi

scientists broke down and told the truth. Rihab Taha had trained in Britain

and spoke excellent English. She told them that Iraq began its biological

weapons program in 1988, just as the Iran-Iraq War was coming to an

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end. Production of germ agents began the next year. Since then, thousands

of gallons of anthrax and botulinum had been produced at Al Hakam. The

anthrax and botulinum were stored in stainless-steel tanks in a warehouse.

Kamel exits. On August 8, Lieutenant General Hussein Kamel, a son-inlaw

of Saddam Hussein, defected to Jordan. He was the highest-level Iraqi

official to escape, and had been in charge of much of the special weapons

program.

Fearing that Kamel would provide the West with some inaccuracies,

Baghdad hurriedly decided to “discover” a cache of his papers, to which

they led the UNSCOM inspectors. A massive amount of information was

there.

(Shortly thereafter, when Saddam promised his son-in-law a warm, loving

welcome, Kamel returned to Baghdad, only to be shot dead by Saddam.)

Gulf War Syndrome. By 1995, thousands of Persian Gulf War veterans

were complaining of a mysterious sickness which seemed to be ruining

their lives. They insisted that their illnesses were caused by the medicines

they were given, the air they breathed, or the anthrax inoculation. But

poor records had been kept of which soldiers had received the anthrax and

botulinum shots during the war.

Faulty records. Were the anthrax shots, given to our troops during the

Gulf War, part of the cause of Gulf War Syndrome? In 1990, about 268,000

doses were sent to the military, but it reported that only 170,000 or less

were given to our troops. Where are the rest? Between 1991 and April

1999, an additional 1.2 million doses were sold to our military.

Said to cause “little harm.” On October 20, 1995, a Defense Department

slide showed a 1.3% systemic-reaction level from the anthrax vaccine.

This was shown to demonstrate that little harm could come to America’s

forces, if the anthrax vaccine was given. However, based on 2.4 million

troops, that would equal 31,200 troops with varying degrees of sickness!

Nerve gas explosions. On June 21, 1996, the Pentagon made an startling

announcement. For nearly five years, it had denied that any one serving

in the Gulf War had been exposed to chemical or biological weapons.

Now they admitted that, after American soldiers blew up an Iraqi ammunition

depot containing chemical weapons, tens of thousands of allied soldiers

might have been exposed to nerve gas. It was believed that prevailing

winds may have blown it toward them.

Checking further, government experts found a second incident in which

allied soldiers had blown up chemical weapons.

Anthrax for all. By the fall of 1996, the Joint Chiefs of Staff at the

Pentagon reversed themselves and approved a recommendation to vaccinate

the entire U.S. military force with anthrax vaccine. The cost would be

$2 billion. Six injections were to be taken by each of 2.4 million American

military personnel.

Not so fast. Bitter complaints arose from the Gulf War veterans who said

it was the anthrax shots which caused at least part of their health problems!

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Medical experts also complained. They declared that the anthrax vaccine

had not been proven by testing to safeguard against the aerosolized

(air sprayed) form of the disease, the kind inhaled by the lungs. (The other

type is the much milder form of the disease which falls on the skin and

burrows in, a type not likely to be included in weaponized anthrax.)

Then the FDA got into the quarrel, arguing that the Michigan anthrax

vaccine building did not follow its own manufacturing procedures, had

rusting equipment, and a dirty environment with floors and even equipment

not sanitized.

Demands were made that the current, entire Pentagon stockpile of anthrax

vaccine doses be tested for sterility, potency, and safety. But the

Pentagon balked. They knew that testing would reveal serious problems,

and they wanted to get on with the vaccinations.

In order to obtain a better report, the Pentagon sent its own inspection

team to the Michigan plant. Military officials feared that, even if problems

were found with the vaccine, if the plant did not keep producing vaccine,

it would close its doors. Then where would they turn to for vaccine? All

the regular pharmaceutical firms had steadfastly refused to manufacture it,

knowing that the anthrax vaccine could cause health problems in those

receiving it, Efforts to begin vaccinating all our soldiers screeched to a

halt.

Weber learns more. In June 1997, Andy Weber went to Kirov in eastern

Russia in order to attend an international meeting of science researchers,

sponsored by the United States, Europe, and Japan.

One evening after a conference session, Weber went to a large cedarpanel

sauna (steam bath). Evesdropping bugs don’t work well in such places.

There he met two Russian scientists of the Obolensk State Research Center

of applied Microbiology. They told him confidentially that at Obolensk, two

hours drive from Moscow, the Soviets in earlier years had perfected dozens

of strains of deadly bacteria for weaponization.

Iranian offers. They also told him that a delegation of Iranians had

recently visited Obolensk and Vector (an important former germ warfare

center which studied viruses, not bacteria). The scientists, who made less

than $1,000 a year, had been offered salaries of up to $5,000 a month if

they would come to Iran and help them on their germ warfare program.

The Iranians said they, the Iranians, were interested in developing germ

and chemical weapons, to be used not only against people but crops and

livestock. They also were interested in Russian genetic engineering.

Ominous developments. Several impoverished Russians from Moscow

institutions had already accepted positions in Iran or agreed to provide it

with information by computer.

Obolensk alone had lost 54% of its staff between 1990 and 1996, including

28% of its top scientists. How many had gone to Iran or some

other foreign country was unknown. (U.S. intelligence sources learned that

similar offers had come from Iraq and North Korea.)

At the time Weber was told this, Washington was spending much less

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than $1 million a year, helping Russian biologists. This was very small,

considering that there were over 15,000 Russian biologists; most of them

were trained in research and development of biological weapons.

After the Kirov conference, Weber traveled to other places in Russia. At

almost every stop, he learned that Iranian agents had been there already,

making offers for workers.

One Russian scientist told Weber that, by the year 2015, Russia would

be 60% Muslim. Fearful of a Muslim takeover, Russian leaders had secretly

moved their stockpiles of exotic disease germs from the designated repository

in Moscow to Vector, which was in faraway central Siberia.

Finally inside Vector. In September 1997, Weber was at last permitted

to investigate what was inside Vector, that immense facility with over a

hundred buildings, located in a desolate part of western Siberia. Many

meetings by Weber in Russia and conferences of officials in Washington

followed.

Joint research projects. Finally, in the fall of 1997, the U.S. agreed that

it should begin joint research projects with scientists at Vector. In this way,

the U.S. could learn more about what was taking place and try to prevent

Iran, Iraq, or China from getting its scientists.

Soon after, similar agreements were entered into with Obolensk and

other Russian research centers.

By this time, samples brought back from the eleven burial pits on the

island of Vozrozhdeniye in the Aral Sea definitely revealed that some of

that massive cache of buried anthrax, just below the surface, was still alive

and deadly.

Still secret labs. Unfortunately, by early 1998, U.S. analysts noted that

four leading Russian military labs remained totally closed to the Americans.

It was feared that some of the money used to help scientists at the

other labs would be shared with the military labs. We had no idea what was

happening in them.

Smallpox contract. In late November 1997, the Pentagon awarded a

$322 million, ten-year contract to DynPort, a British-American firm, to

develop and obtain licenses for smallpox and 17 other vaccines for the

military, plus a new recombinant anthrax vaccine.

New anthrax campaign. On December 15, the Pentagon announced that

the vaccination of the entire U.S. military against anthrax was to begin

soon. It would take six years and cost $130 million.

Soon after, the Michigan plant was purchased by BioPort; this was owned

by the wealthy Iranian, Fuad El-Hibri, with Myers and Ravenswaay on the

board. But it still did not seem to know how to properly manufacture

anthrax vaccine. When Pentagon officials were asked about the sloppy work

at the plant, they consistently sidestepped the question. The truth was

that the Michigan plant was their only source, and they intended to use

the vaccine coming from it, regardless of its quality controls.

Many anthrax strains. In view of all that you have learned so far in this

study, you might ask, If the enemy has so many different types of danger-

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ous bioweapons, knowing that our troops are to be vaccinated against anthrax,

why would not the enemy use a different agent against us—smallpox,

ebola, bubonic plague, or something else? The answer to such a sensible

question is quite obvious.

It is a known fact that there are over 1,000 different strains of anthrax

(Care McNair, Dynport Vaccine Company, Maryland, quoted in Dave

Eberhart, Anthrax, October 29, 2001).

Genetically modified anthrax. Much of what the defector, Ken Alibek,

had told our intelligence in 1992 had been ignored. One thing he had said

was that Russia was continuing to find ways to blend ebola and smallpox.

But the December 1997 issue of Vaccine (pp. 1846-1850), a London-based

scientific journal, disclosed that Russian research had produced genetically

modified anthrax. The Russian strains of Bacillus anthracis and Bacillus

cereus were found to be closely related and often in soils near one

another. Based on that fact, the project was successfully carried through to

completion.

Russia, it turned out, was far more advanced in some areas of recombinant

research than we had assumed. U.S. military men and scientists were

alarmed to discover that Russia was in the process of making “super bugs”!

Alibek goes public. In February 1998, in interviews with the New York

Times and ABC’s Prime Time Live, Ken Alibek went public with the frightening

news of what was happening inside Russian biowarfare labs. He said

the Soviet Union had planned that World War III include “hundreds of

tons” of anthrax bacillus and scores of tons of smallpox and plague viruses.

He also said that the Soviet labs had made hybrid germs from ebola and

smallpox, which no vaccine or antibiotic could protect against. Many Washington

legislators did not know that Alibek even existed.

Pscho germs. A new development was the discovery about the time of

the former Soviet Union effort to use genetically engineered germs and

toxins to cause psychological and physiological changes in people. The

program involved making changes in peptides (short chains of amino acids

that send signals to the central nervous system), to alter moods, sleep

patterns, and heart rhythms—all without detection. They could also be

used to produce death. The discovery was also made that these drugs were

being used on patients in a hospital located close to that Russian research

center!

Smallpox canisters. Soon after, we found that smallpox had also been

tested on that Aral island, and that large amounts of it were also buried in

canisters there.

Rapid-reaction teams. On March 17, 1998, Secretary of Defense Cohen

announced that the National Guard was preparing ten rapid-reaction teams

which would rush to any locality in America attacked by chemical or biological

weapons.

25 nations. He went public with the fact that 25 nations had or were

developing chemical and biological weapons, and the expertise was spreading

rapidly through the internet. He said terrorist groups would eventually

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be able to acquire those weapons. Soon after, Congress lavished money on

the new state guard program.

Vaccinations resumé. In March 1998, the Pentagon began vaccinating

our troops in the Near East against anthrax. But over two dozen sailors on

two U.S. navy carriers refused them, fearing for their own health. They

were about to be court-martialed, but managed to get e-mails to Mark Zaid,

an extremely competent Washington-based attorney who was already handling

a case about the Gulf War Syndrome cover-up.

Zaid makes discoveries. Zaid filed a lawsuit under FIA (Freedom of

Information Act) for every document connected to the anthrax vaccine

program.

He quickly found that, in 1998, the Michigan vaccine facility had been

sold BioPort, a new company whose owners included Willam J. Crowe, Jr.,

the former chairman of the Joint Chiefs of Staff. Government contracts for

massive quantities of anthrax vaccine could be lucrative.

Zaid also discovered that, for years, the FDA had been reporting on

deficiencies at that Michigan plant. The latest inspection, on February 1998,

was not much better. Many deficiencies still needed to be corrected. There

was something wrong with almost every phase of the production process.

—Yet its vaccines were already being injected into U.S. servicemen overseas!

He also learned that the anthrax vaccine had been significantly altered.

The new vaccine was quite different from the original one. The manufacturing

process was changed, the strain of anthrax was different, and the

added ingredients were changed “in order to increase the yield of protective

antigen” (Heemstra, Anthrax, pp. 18-19).

Another researcher, Redmond Handy, uncovered many secret U.S. files.

For example, one document from Fort Detrick revealed this:

“There is no vaccine in current use which will safely and effectively protect military

personnel against exposure to this hazardous bacterial agent.” “Highly reactogenic,

[it] requires multiple boosters to maintain immunity and may not be protective against

all strains of the anthrax bacillus” (Redmond Handy, “Analysis of DOD’s Anthrax

Vaccine Immunization Program (AVIP),” report presented at the Call for Amnesty

Press Conference, Washington, D.C., February 12, 2001, p. 7).

Delayed approval. It was not until two months after the military began

vaccinating troops for anthrax that, in May 1998, Secretary Cohen officially

gave approval for it to be done.

U.S. military within U.S. In the latter part of June, John Hamre, Secretary

of Defense, told NATO officials that the Pentagon was thinking of appointing

a regional commander to be in charge of “homeland defense.” The

plan was, in case of a bioweapons attack, to send the national guard to set

up field hospitals, bury the dead, and help care for the living.

But civil liberties experts were alarmed and, pointing to the Posse Comitatus

Act enacted after the Civil War, declared it would be illegal for the

federal government to interfere with activities within the states. The U.S.

military would be involved in domestic law enforcement. The Pentagon

immediately backed down. It would not be until 2002 that a Homeland

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Security Agency would finally be enacted into law.

$2 billion requested. On January 22, 1999, Clinton announced his

decision to ask Congress for $2.8 billion to avoid and prepare for biochemical

attacks. Donna Shalala, Secretary for Health and Human Services,

commented that it was the first time in U.S. history that the publicheath

system was being integrated into national-security planning.

Our stockpiles not destroyed. It was only a few months later that the

White House had to decide whether America should destroy its remaining

stocks of smallpox virus. But experts immediately stepped forward, declaring

that not only Russia but other nations had smallpox stockpiles. A special

committee, formed by the National Academy of Science to study the

matter, decided in March that it was not wise to destroy our smallpox

stocks.

Shocking facts. About a month later, William Patrick, a germ weapons

expert, revealed a few facts to a special military conference at Maxwell Air

Force Base:

Dry agent production (in metric tons per year) during peak production

periods by the U.S. and former Soviet Union (S.U.):

Tularemia: U.S. 1.6 / S.U. 15,000

Q fever: U.S. 1.1 / S.U. 0

Anthrax: U.S. 0.9 / S.U. 45,000

Encephalitis: U.S. 0.8 / S.U. 150

Botulinum: U.S. 0.2 / S.U. 0

bubonic plague: U.S. 0 / S.U. 15,000

smallpox: U.S. 0 / S.U. 100

Glanders: U.S. 0 / S.U. 2,000

Marburg virus: U.S. 0 / S.U. 250

Exposure to no more than 10,000 anthrax germs—all of which would

fit comfortably into the period at the end of this sentence—could kill a

human being. The spores are so tiny, they can slip through the fibers of an

envelope or sheet of paper.

Zaid goes public. Meanwhile, the anthrax vaccine crisis only deepened.

Mark Zaid, the attorney representing some of the first soldiers who refused

the vaccine, had obtained thousands of pages of damaging facts about it.

He began issuing press releases about his findings and sharing copies with

the media.

Soldiers refuse vaccine. By this time, hundreds of soldiers, fearing for

their health, had refused orders to take the shots. Fearing that their example

would produce a general rebellion, the military took steps to courtmartial

them.

The problem had been worsened by a spring 1998 decision by the Pentagon,

“in the interest of fairness,” to also vaccinate reservists who were

not stationed in high-risk areas.

Pilots quit. This decision especially angered pilots in the Air National

Guard. Many had jobs back home flying for commercial airlines. Strong

and healthy, they feared for their personal safety.

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Over 260 pilots quit the Air National Guard or Air Force Reserve. The

GAO predicted a 43% total loss of pilots over the next six months. At a cost

of $6 million to train each of these combat-ready pilots with eight to ten

years of experience, the total cost was $1.5 billion.

GAO testimony. At an April 1999 hearing before Chris Shay’s house

subcommittee, a GAO (General Accounting Office) auditor told the congressmen

that no study had ever been made of the long-term safety of the

anthrax vaccine. “Therefore one cannot conclude there are no long-term

effects,” he said. He also stated that there were questions about how effective

it was in protecting against an anthrax attack. It appeared that the

vaccine was both dangerous and useless.

Another GAO official, Sushil Sharma, revealed that the Defense

Department’s brochure about the vaccine was not true when it said that

the vaccine had already been given to large numbers of “veterinarians,

laboratory workers, and livestock handlers.” It had actually been given to

only a few.

Records missing. It was also discovered that there was no record of who

received the anthrax shots in the Gulf War, yet the Pentagon had been

claiming for years that the Desert Storm illnesses were not caused by the

vaccine (Hearing before the Subcommittee on National Security, Veterans

Affairs, and International Relations of the Committee on Government Reform,

106th Cong., 1st sess., Apr. 29, 1999, pp. 10-20).

Protecting BioPort. As if that was not bad enough, Zaid, the attorney,

disclosed that he had come across documents which had been drafted

earlier by the army in order to indemnify companies making the anthrax

vaccine! BioPort in Michigan was so afraid of the dangers of the anthrax

vaccine it was manufacturing, it wanted governmental protection against

lawsuits that would pour in when Americans were injured by receiving it

or when it proved ineffective in protecting against an anthrax attack!

Long-term study promised. The Pentagon replied that there really was

nothing to worry about, but a month later it promised to begin “a longterm

study” of the vaccine’s safety. This was more than a year after large

quantities of the shots began to be given and nine years after it had been

given during the Gulf War. We are still waiting for that study to begin.

BioPort in trouble. More trouble erupted in the autumn of 1999, when

BioPort, the Michigan company churning out the vaccine, was unable to

meet FDA standards. So far, that plant never had met them. But this time,

the FDA threatened to close down its operations.

There was danger that the firm might become financially insolvent. So,

to help the company financially (not to improve the safety of the vaccine),

the Pentagon agreed to raise the price of what it was paying the firm per

anthrax dose, from $4.36 to $10.64.

This gave the company an additional $24 million; $18.7 million of this

was immediately paid in advance. You will recall that it was BioPort which

earlier spent millions on office furniture for its executives and bonuses for

its executives.

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Vaccine still flunking tests. Shortly after this, it was discovered that

nearly 1.5 million vaccine doses, manufactured at BioPort, did not pass

potency tests. Others were rejected by the FDA because it had not followed

sterility procedures! A new inspection report found over 30 deficiencies,

including the fact that batches did not uniformly meet the same specifications.

House report. The house committee investigating the anthrax vaccine

issued a special report in April 2000: “The Department of Defense Anthrax

Vaccine Immunization Program: Unproven Force Protection.”

Strains not defendable against vaccine. The report included the very

serious fact that gene splicing by an enemy could easily produce a strain of

anthrax which would be completely resistant to our anthrax vaccine, making

the program a “medical Maginot Line, a fixed fortification protecting

against attack from only one direction.” In other words, it was a waste of

time to inject Americans—any Americans—with anthrax vaccine (Committee

on Government Reform, 106th Cong., 2d sess., House Report 106-556,

April 3, 2000, p. 2).

Could the same be true about the other biowarfare protection vaccines?

One example should suffice:

Variant U. In the spring of 1988, Nikolai Ustinov had died at Vector, the

Siberian smallpox research complex. He was a scientist who had accidentally

infected himself with the Marburg virus, a hemorrhagic killer that he

and his colleagues had been trying to perfect as a weapon. After his death,

his colleagues at Vector had cultured the virus that killed him. They discovered

that, inside his body the virus had changed slightly. The new variant,

according to Ken Alibek, was particularly virulent and had been

weaponized as a replacement for the original. In Ustinov’s honor, it was

named “Variant U.” In addition, any vaccine prepared to defend against

Marburg virus would be useless against Marburg-U virus.

It was not difficult to produce disease variants which vaccines could

not protect against. We would have to have samples of the secret virus;

and, even if we made a vaccine, which could take years, there was a good

likelihood it would neither be safe nor protective. We were already discovering

that with our anthrax and smallpox vaccines.

2000 AND A NEW CRISIS

“Unknown effects.” A March 2000 study, released by the Institute of

Medicine at the National Academy of Sciences, concluded that there was

“inadequate/insufficient evidence” to determine whether the anthrax vaccine

could cause “long-term adverse health outcomes.” It added that there

was a “paucity of published, peer-reviewed literature,” and those few reports

only described “a few short-term studies” (NAS Institute of Medicine,

“An assessment of the Safety of the Anthrax Vaccine, A Letter Report,”

Washington, D.C., March 30, 2000, pp. 5-6). In other words, almost

no research had ever been done about the safety or effectiveness of the

strain of anthrax vaccine we had, and no long-term studies had ever been

made!

Glossary

Glossary

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No official clinical research had ever been done to prove anything. But,

of course, there were thousands of service men and women known to have

been damaged by the vaccine.

More pilots quit. By this time, hundreds of reserve pilots had quit the

military. By the summer of 2000, over 400 servicemen had been disciplined

for refusing to take the shots, and 51 had been court-martialed. A

few served brief sentences in the brig.

Only the U.S. military. Because of the extreme dangers of these antiattack

vaccines, no other nation in the world required its troops to be

vaccinated, not one! Britain made anthrax vaccinations for its troops voluntary,

and France did not give them at all.

Mock bio-attacks. In the spring of 2000, 10-day mock bio-attacks were

staged in Portsmouth, New Hampshire, and Denver, Colorado. Much of this

was done on paper, some in practice sessions.

The exercise in Denver ended on May 23, as the make-believe “epidemic”

spread out of control. Estimates of how many people would have

gotten sick varied widely. Some said 3,700 plague cases with 950 deaths;

others estimated more than 4,000 sick and 2,000 dead. Federal, state, and

local officials quickly proclaimed the catastrophe a successful exercise. The

entire operation cost $10 million.

Interesting question. One problem was whether scarce resources should

be devoted to treating the sick who might die or trying to stop the spread

of the epidemic. At least the government discovered that it had lots of

unanswered questions.

How the money was spent. In the fall of 2000, Amy Smithson, an analyst

at the Henry L. Stimson Center in Washington, conducted an 18-

month investigation; and, among other things, he found that only $315

million of the $8.4 billion the government spent on counterterrorism in

the year 2000 was devoted to training people in cities and states to respond

to a covert bioterrorism attack. Less than 4% of that amount was

being spent outside of Washington, D.C., and only 6% to strengthen public-

health facilities, the heart of useful biodefense preparedness. The rest

was spent on faulty detectors, special vehicles, and other marginal items

(Amy Smithson and Leslie-Anne Levy, Ataxia: The Chemical and Biological

Terrorism Threat and the U.S. Response, Henry L. Stimson Center). Lots of

money was being misdirected to objectives which would not protect the

public.

Teams set up. By January 2001, more than $143 million had been

spent on rapid-reaction teams (renamed Civil Support Teams) within the

National Guard. Each one was located on a military base, and many were

long distances from the cities they were supposed to protect. (The closest

one to Atlanta was 250 miles away in Florida.)

After the September 11 tragedy occurred, everything speeded up, but

there was much confusion as to what should be done, how it should be

done, who should be in charge, and how should they cooperate with one

another.

Bibliography

Bibliography

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Bibliography

Protecting another vaccine firm. In the fall of 2002, a last-minute addition

was made in secret the night before the last major budget bill (the

Homeland Defense Security Act) was passed by Congress. The addition

released Eli Lilly & Co. from liability for damage from vaccines it sold to

the public and to the military.

WHAT IS THE SOLUTION?

What is the answer? In this chapter, we have overviewed a massive

problem, caused by production of dangerous biological weapons. What is

the answer? Are there solutions, and what are they?

Treatment, not vaccination. If rapid detection, diagnosis, and treatment

methods are in place, people exposed to anthrax can be cured of the

disease. That is part of the solution. Not vaccination, but immediate treatment

of the sick!

Vaccination cannot protect against multiple strains. In Sverdlovsk, Russia,

when anthrax was accidentally released from a biowarfare facility in

1979, when the spore cloud passed directly over a nearby ceramics factor

shop, only 10 out of 450 workers fell ill and died. This was a fatality rate of

only 2% (Redmond Handy, “Analysis of DOD’s Anthrax Vaccine Immunization

Program [AVIP],” report to Call for Amnesty Press Conference, Washington,

D.C., February 12, 2001, p. 49).

Later at the Los Alamos National Laboratory in New Mexico, autopsy

studies were made of some of those 10 people. It revealed that they were

infected by at least four different strains of anthrax. This means that no

vaccine could have protected against such an attack!

One scientist, Paul Jackson, concluded, “The purpose of such a mixture

might have been to overwhelm the American vaccine” (Jackson, quoted

in Nicholas Wade, “Tests with Anthrax Raise Fears that American Vaccine

Can be Defeated,” New York Times National, March 26, 1998).

Vaccination cannot protect against genetically altered strains. The Russians

had developed a special combined strain which would defy any vaccine

we could make against it. It is known that they have also made genealtered

strains that could defeat their own vaccine, not only ours; this is

much more powerful.

The experts agree. Testifying before Congress in the spring of 1998,

Ken Alibek, the former deputy director of the Soviet biological warfare

directorate (BioParat), said, “We need to stop deceiving people that vaccines

are the most effective protection . . In the case of most military and

all terrorist attacks with biological weapons, vaccines would be of little

use” (Dr. Ken Alibek, statement to Joint Economic Committee of Congress,

May 20, 1998).

Our leaders have known this for a long time. In a test done at Fort

Detrick in 1986, guinea pigs were immunized with our U.S. anthrax vaccine

and then given several different anthrax strains. Half of themdied.

In a separate Fort Detrick study, over 50% of the guinea pigs died.

Here is an intriguing statement by an expert at a major U.S. vaccine

firm: “The great challenge was to manufacture a vaccine that will be effe