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Unit 731 – Wikipedia

Posted: November 14, 2016 at 11:42 am

Unit 731 (Japanese: 731, Hepburn: Nana-san-ichi Butai?) was a covert biological and chemical warfare research and development unit of the Imperial Japanese Army that undertook lethal human experimentation during the Second Sino-Japanese War (19371945) of World War II. It was responsible for some of the most notorious war crimes carried out by Japan. Unit 731 was based at the Pingfang district of Harbin, the largest city in the Japanese puppet state of Manchukuo (now Northeast China).

It was officially known as the Epidemic Prevention and Water Purification Department of the Kwantung Army (, Kantgun Beki Kysuibu Honbu?). Originally set up under the Kempeitai military police of the Empire of Japan, Unit 731 was taken over and commanded until the end of the war by General Shiro Ishii, an officer in the Kwantung Army. The facility itself was built between 1934 and 1939 and officially adopted the name "Unit 731" in 1941.

Some historians estimate that up to 250,000[1] men, women, and children[2][3]from which around 600 every year were provided by the Kempeitai[4]were subjected to experimentation conducted by Unit 731 at the camp based in Pingfang alone, which does not include victims from other medical experimentation sites, such as Unit 100.[5]

Unit 731 veterans of Japan attest that most of the victims they experimented on were Chinese[6] while a small percentage were Russian, Mongolian, Korean, and Allied POW's.[7] Almost 70% of the victims who died in the Pingfang camp were Chinese, including both civilian and military.[8] Close to 30% of the victims were Russian.[9] Some others were South East Asians and Pacific Islanders, at the time colonies of the Empire of Japan, and a small number of Allied prisoners of war.[10] The unit received generous support from the Japanese government up to the end of the war in 1945.

Instead of being tried for war crimes, the researchers involved in Unit 731 were secretly given immunity by the U.S. in exchange for the data they gathered through human experimentation.[11] Others that Soviet forces managed to arrest first were tried at the Khabarovsk War Crime Trials in 1949. Americans did not try the researchers so that the information and experience gained in bio-weapons could be co-opted into the U.S. biological warfare program, as had happened with Nazi researchers in Operation Paperclip.[12] On 6 May 1947, Douglas MacArthur, as Supreme Commander of the Allied Forces, wrote to Washington that "additional data, possibly some statements from Ishii probably can be obtained by informing Japanese involved that information will be retained in intelligence channels and will not be employed as 'War Crimes' evidence."[11] Victim accounts were then largely ignored or dismissed in the West as communist propaganda.[13]

A special project code-named Maruta used human beings for experiments. Test subjects were gathered from the surrounding population and were sometimes referred to euphemistically as "logs" (, maruta?), used in such contexts as "How many logs fell?". This term originated as a joke on the part of the staff because the official cover story for the facility given to the local authorities was that it was a lumber mill. However, in an account by a man who worked as a junior uniformed civilian employee of the Japanese Army in Unit 731, the project was internally called "Holzklotz", which is the German word for log.[14]

The test subjects were selected to give a wide cross-section of the population and included common criminals, captured bandits and anti-Japanese partisans, political prisoners, and also people rounded up by the Kempeitai military police for alleged "suspicious activities". They included infants, the elderly, and pregnant women.

Thousands of men, women and children interred at prisoner of war camps were subjected to vivisection, often without anesthesia and usually ending with the death of the victim.[15] Vivisections were performed on prisoners after infecting them with various diseases. Researchers performed invasive surgery on prisoners, removing organs to study the effects of disease on the human body. These were conducted while the patients were alive because it was feared that the decomposition process would affect the results.[16] The infected and vivisected prisoners included men, women, children, and infants.[17]

Prisoners had limbs amputated in order to study blood loss. Those limbs that were removed were sometimes re-attached to the opposite sides of the body. Some prisoners' limbs were frozen and amputated, while others had limbs frozen, then thawed to study the effects of the resultant untreated gangrene and rotting.

Some prisoners had their stomachs surgically removed and the esophagus reattached to the intestines. Parts of the brain, lungs, liver, etc., were removed from some prisoners.[15]

Japanese army surgeon Ken Yuasa suggests that the practice of vivisection on human subjects (mostly Chinese communists) was widespread even outside Unit 731,[6] estimating that at least 1,000 Japanese personnel were involved in the practice in mainland China.[18]

Prisoners were injected with inoculations of disease, disguised as vaccinations, to study their effects. To study the effects of untreated venereal diseases, male and female prisoners were deliberately infected with syphilis and gonorrhea, then studied. Prisoners were also repeatedly subject to rape by guards.[19]

Plague fleas, infected clothing, and infected supplies encased in bombs were dropped on various targets. The resulting cholera, anthrax, and plague were estimated to have killed around and possibly more than 400,000 Chinese civilians.[20]Tularemia was tested on Chinese civilians.[21]

Unit 731 and its affiliated units (Unit 1644 and Unit 100 among others) were involved in research, development, and experimental deployment of epidemic-creating biowarfare weapons in assaults against the Chinese populace (both civilian and military) throughout World War II. Plague-infested fleas, bred in the laboratories of Unit 731 and Unit 1644, were spread by low-flying airplanes upon Chinese cities, coastal Ningbo in 1940, and Changde, Hunan Province, in 1941. This military aerial spraying killed thousands of people with bubonic plague epidemics.[22]

It is possible that Unit 731's methods and objectives were also followed in Indonesia, in a case of failed experiment designed to validate a conjured tetanus toxoid vaccine.[23]

Physiologist Yoshimura Hisato conducted experiments by taking captives outside, dipping various appendages into water, and allowing the limb to freeze. Once frozen, which testimony from a Japanese officer said "was determined after the 'frozen arms, when struck with a short stick, emitted a sound resembling that which a board gives when it is struck'",[24] ice was chipped away and the area doused in water. The effects of different water temperatures were tested by bludgeoning the victim to determine if any areas were still frozen. Variations of these tests in more gruesome forms were performed.

Doctors orchestrated forced sex acts between infected and non-infected prisoners to transmit the disease, as the testimony of a prison guard on the subject of devising a method for transmission of syphilis between patients shows:

"Infection of venereal disease by injection was abandoned, and the researchers started forcing the prisoners into sexual acts with each other. Four or five unit members, dressed in white laboratory clothing completely cover the body with only eyes and mouth visible, handled the tests. A male and female, one infected with syphilis, would be brought together in a cell and forced into sex with each other. It was made clear that anyone resisting would be shot."[25]

After victims were infected, they were vivisected at different stages of infection, so that internal and external organs could be observed as the disease progressed. Testimony from multiple guards blames the female victims as being hosts of the diseases, even as they were forcibly infected. Genitals of female prisoners that were infected with syphilis were called "jam filled buns" by guards.[26]

Some children grew up inside the walls of Unit 731, infected with syphilis. A Youth Corps member deployed to train at Unit 731 recalled viewing a batch of subjects that would undergo syphilis testing: "one was a Chinese woman holding an infant, one was a White Russian woman with a daughter of four or five years of age, and the last was a White Russian woman with a boy of about six or seven."[26] The children of these women were tested in ways similar to their parents, with specific emphasis on determining how longer infection periods affected the effectiveness of treatments.

Female prisoners were forced to become pregnant for use in experiments. The hypothetical possibility of vertical transmission (from mother to fetus or child) of diseases, particularly syphilis, was the stated reason for the torture. Fetal survival and damage to mother's reproductive organs were objects of interest. Though "a large number of babies were born in captivity", there has been no account of any survivors of Unit 731, children included. It is suspected that the children of female prisoners were killed or the pregnancies terminated.[26]

While male prisoners were often used in single studies, so that the results of the experimentation on them would not be clouded by other variables, women were sometimes used in bacteriological or physiological experiments, sex experiments, and the victims of sex crimes. The testimony of a unit member that served as guard graphically demonstrates this reality:

"One of the former researchers I located told me that one day he had a human experiment scheduled, but there was still time to kill. So he and another unit member took the keys to the cells and opened one that housed a Chinese woman. One of the unit members raped her; the other member took the keys and opened another cell. There was a Chinese woman in there who had been used in a frostbite experiment. She had several fingers missing and her bones were black, with gangrene set in. He was about to rape her anyway, then he saw that her sex organ was festering, with pus oozing to the surface. He gave up the idea, left, and locked the door, then later went on to his experimental work."[26]

Human targets were used to test grenades positioned at various distances and in different positions. Flame throwers were tested on humans. Humans were tied to stakes and used as targets to test germ-releasing bombs, chemical weapons, and explosive bombs.[27][28]

In other tests, subjects were deprived of food and water to determine the length of time until death; placed into high-pressure chambers until death; experimented upon to determine the relationship between temperature, burns, and human survival; placed into centrifuges and spun until death; injected with animal blood; exposed to lethal doses of x-rays; subjected to various chemical weapons inside gas chambers; injected with sea water; and burned or buried alive.[29]

Japanese researchers performed tests on prisoners with Bubonic plague, cholera, smallpox, botulism, and other diseases.[30] This research led to the development of the defoliation bacilli bomb and the flea bomb used to spread bubonic plague.[31] Some of these bombs were designed with porcelain shells, an idea proposed by Ishii in 1938.

These bombs enabled Japanese soldiers to launch biological attacks, infecting agriculture, reservoirs, wells, and other areas with anthrax, plague-carrier fleas, typhoid, dysentery, cholera, and other deadly pathogens. During biological bomb experiments, researchers dressed in protective suits would examine the dying victims. Infected food supplies and clothing were dropped by airplane into areas of China not occupied by Japanese forces. In addition, poisoned food and candies were given out to unsuspecting victims, and the results examined.

In 2002, Changde, China, site of the flea spraying attack, held an "International Symposium on the Crimes of Bacteriological Warfare" which estimated that at least 580,000 people died as a result of the attack.[32] The historian Sheldon Harris claims that 200,000 died.[33] In addition to Chinese casualties, 1,700 Japanese in Chekiang were killed by their own biological weapons while attempting to unleash the biological agent, which indicates serious issues with distribution.[2]

During the final months of World War II, Japan planned to use plague as a biological weapon against San Diego, California. The plan was scheduled to launch on September 22, 1945, but Japan surrendered five weeks earlier.[34][35][36][37]

Despite the facility's location in Northern China, great pains were taken by organizers of the facility that its inmates represented a wide array of ethnicities. Most of the prisoners of war were American.[38]

Robert Peaty (19031988), a British Major in the Royal Army Ordnance Corps, was the senior ranking allied officer. During this time, he kept a secret diary. A copy of his entire diary exists in the NARA archives.[39] An extract of the diary is available at the UK National Archives at Kew.[40] He was interviewed by the Imperial War Museum in 1981, and the audio recording tape reels are in the IWM's archives.[41]

Unit 731 was divided into eight divisions:

The Unit 731 complex covered six square kilometres (2.3 square miles) and consisted of more than 150 buildings. The design of the facilities made them hard to destroy by bombing. The complex contained various factories. It had around 4,500 containers to be used to raise fleas, six cauldrons to produce various chemicals, and around 1,800 containers to produce biological agents. Approximately 30 kilograms (66 pounds) of bubonic plague bacteria could be produced in a few days.

Some of Unit 731's satellite facilities are in use by various Chinese industrial concerns. A portion has been preserved and is open to visitors as a War Crimes Museum.

A medical school and research facility belonging to Unit 731 operated in the Shinjuku District of Tokyo during World War II. In 2006, Toyo Ishiia nurse who worked at the school during the warrevealed that she had helped bury bodies and pieces of bodies on the school's grounds shortly after Japan's surrender in 1945. In response, in February 2011 the Ministry of Health began to excavate the site.[43]

China requested DNA samples from any human remains discovered at the site. The Japanese governmentwhich has never officially acknowledged the atrocities committed by Unit 731rejected the request.[44]

The related Unit 8604 was operated by the Japanese Southern China Area Army and stationed at Guangzhou (Canton). This installation conducted human experimentation in food and water deprivation as well as water-borne typhus. According to postwar testimony, this facility served as the main rat breeding farm for the medical units to provide them with bubonic plague vectors for experiments.[45]

Unit 731 was part of the Epidemic Prevention and Water Purification Department which dealt with contagious disease and water supply generally.

Operations and experiments continued until the end of the war. Ishii had wanted to use biological weapons in the Pacific War since May 1944, but his attempts were repeatedly snubbed.

With the coming of the Red Army in August 1945, the unit had to abandon their work in haste. The members and their families fled to Japan.

Ishii ordered every member of the group "to take the secret to the grave", threatening to find them if they failed, and prohibiting any of them from going into public work back in Japan. Potassium cyanide vials were issued for use in the event that the remaining personnel were captured.

Skeleton crews of Ishii's Japanese troops blew up the compound in the final days of the war to destroy evidence of their activities, but most were so well constructed that they survived somewhat intact.

Among the individuals in Japan after their 1945 surrender was Lieutenant Colonel Murray Sanders, who arrived in Yokohama via the American ship Sturgess in September 1945. Sanders was a highly regarded microbiologist and a member of America's military center for biological weapons. Sanders' duty was to investigate Japanese biological warfare activity. At the time of his arrival in Japan he had no knowledge of what Unit 731 was.[26] Until Sanders finally threatened the Japanese with bringing communism into the picture, little information about biological warfare was being shared with the Americans. The Japanese wanted to avoid the Soviet legal system so the next morning after the threat Sanders received a manuscript describing Japan's involvement in biological warfare.[46] Sanders took this information to General Douglas MacArthur, who was the Supreme Commander of the Allied Powers responsible for rebuilding Japan during the Allied occupations. MacArthur struck a deal with Japanese informants[47]he secretly granted immunity to the physicians of Unit 731, including their leader, in exchange for providing America, but not the other wartime allies, with their research on biological warfare and data from human experimentation.[11] American occupation authorities monitored the activities of former unit members, including reading and censoring their mail.[48] The U.S. believed that the research data was valuable. The U.S. did not want other nations, particularly the Soviet Union, to acquire data on biological weapons.[49]

The Tokyo War Crimes Tribunal heard only one reference to Japanese experiments with "poisonous serums" on Chinese civilians. This took place in August 1946 and was instigated by David Sutton, assistant to the Chinese prosecutor. The Japanese defense counsel argued that the claim was vague and uncorroborated and it was dismissed by the tribunal president, Sir William Webb, for lack of evidence. The subject was not pursued further by Sutton, who was probably unaware of Unit 731's activities. His reference to it at the trial is believed to have been accidental.

Although publicly silent on the issue at the Tokyo Trials, the Soviet Union pursued the case and prosecuted twelve top military leaders and scientists from Unit 731 and its affiliated biological-war prisons Unit 1644 in Nanjing, and Unit 100 in Changchun, in the Khabarovsk War Crime Trials. Included among those prosecuted for war crimes, including germ warfare, was General Otoz Yamada, the commander-in-chief of the million-man Kwantung Army occupying Manchuria.

The trial of those captured Japanese perpetrators was held in Khabarovsk in December 1949. A lengthy partial transcript of the trial proceedings was published in different languages the following year by a Moscow foreign languages press, including an English language edition.[50] The lead prosecuting attorney at the Khabarovsk trial was Lev Smirnov, who had been one of the top Soviet prosecutors at the Nuremberg Trials. The Japanese doctors and army commanders who had perpetrated the Unit 731 experiments received sentences from the Khabarovsk court ranging from two to 25 years in a Siberian labor camp. The U.S. refused to acknowledge the trials, branding them communist propaganda.[51]

After World War II, the Soviet Union built a biological weapons facility in Sverdlovsk using documentation captured from Unit 731 in Manchuria.[52]

As above, under the American occupation the members of Unit 731 and other experimental units were allowed to go free. One graduate of Unit 1644, Masami Kitaoka, continued to do experiments on unwilling Japanese subjects from 1947 to 1956 while working for Japan's National Institute of Health Sciences. He infected prisoners with rickettsia and mental health patients with typhus.[53]

Japanese discussions of Unit 731's activity began in the 1950s, after the end of the American occupation of Japan. In 1952, human experiments carried out in Nagoya City Pediatric Hospital, which resulted in one death, were publicly tied to former members of Unit 731.[54] Later in that decade, journalists suspected that the murders attributed by the government to Sadamichi Hirasawa were actually carried out by members of Unit 731. In 1958, Japanese author Shsaku End published the book The Sea and Poison about human experimentation, which is thought to have been based on a real incident.

The author Seiichi Morimura published The Devil's Gluttony () in 1981, followed by The Devil's Gluttony: A Sequel in 1983. These books purported to reveal the "true" operations of Unit 731, but actually confused them with that of Unit 100, and falsely used unrelated photos attributing them to Unit 731, which raised questions about its accuracy.[55][56]

Also in 1981 appeared the first direct testimony of human vivisection in China, by Ken Yuasa. Since then many more in-depth testimonies have appeared in Japanese. The 2001 documentary Japanese Devils was composed largely of interviews with 14 members of Unit 731 who had been taken as prisoners by China and later released.[57]

Since the end of the Allied occupation, the Japanese government has repeatedly apologized for its pre-war behavior in general, but specific apologies and indemnities are determined on the basis of bilateral determination that crimes occurred, which requires a high standard of evidence. Unit 731 presents a special problem, since unlike Nazi human experimentation which the U.S. publicly condemned, the activities of Unit 731 are known to the general public only from the testimonies of willing former unit members, and testimony cannot be employed to determine indemnity in this way.

Japanese history textbooks usually contain references to Unit 731, but do not go into detail about allegations, in accordance with this principle.[58][59]Saburo Ienaga's New History of Japan included a detailed description, based on officers' testimony. The Ministry for Education attempted to remove this passage from his textbook before it was taught in public schools, on the basis that the testimony was insufficient. The Supreme Court of Japan ruled in 1997 that the testimony was indeed sufficient and that requiring it to be removed was an illegal violation of freedom of speech.[60]

In 1997, the international lawyer Knen Tsuchiya filed a class action suit against the Japanese government, demanding reparations for the actions of Unit 731, using evidence filed by Professor Makoto Ueda of Rikkyo University. All Japanese court levels found that the suit was baseless. No findings of fact were made about the existence of human experimentation, but the decision of the court was that reparations are determined by international treaties and not by national court cases.

In October 2003, a member of the House of Representatives of Japan filed an inquiry. Japanese Prime Minister Junichiro Koizumi responded that the Japanese government did not then possess any records related to Unit 731, but the government recognized the gravity of the matter and would publicize any records that were located in the future.[61]

There have been several films about the atrocities of Unit 731.

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Unit 731 - Wikipedia

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Germ Warfare – No Sweat

Posted: September 29, 2016 at 11:54 am

Germ Warfare

Many hockey players, such as reporter Randy Boswell, are skating biohazards. With bacteria growing on their equipment at up to 3,440 times higher than acceptable levels, they can be a danger to themselves and others, reports Hugh Adami. by Hugh Adami

December 11, 2004

'This is very bad," he said quietly, with a wary look that would make most wonder what horror they were about to be told. Felix Skora unfolded the sheet of paper and slid it across the desk for his guest to see. The information was numbing. Germ warfare. That's what Skora's Gatineau laboratory, Micro B, found in Randy Boswell's hockey bag after we took it there to see if the CanWest News reporter's soppy, rank equipment posed a hazard to his health and to those around him when he's on the ice trying, as he says, to be "an amalgam" of Bobby Orr and Wayne Gretzky. Skora has no idea if Orr and Gretzky had as much disregard for the care of their equipment as Boswell does for his, but suggested some fast action be taken in the laundry room. " There is a need to disinfect this equipment," Skora said. "Possibly with chlorine, alcohol and perhaps washed at a high temperature. Then, you should be able to eliminate the bacteria, the yeast, the mould." What Micro B found lurking about Boswell's equipment was a cesspool of bacterial growth. "Very high concentrations," Skora explained. Dr. Barry Dworkin, who writes a health column for the Citizen, said the bacteria could include numerous types of pathogenic germs, viruses and fungal substances, which can lead to a variety of illnesses and skin infections, some of which he has treated. Sounds good so far, eh? The lab didn't test for moulds and yeast, but Skora said the high bacterial concentrations would virtually guarantee their presence. In fact, said Dr. Dworkin, heat and humidity stimulate growth of fungal matter. Dr. Dworkin also said that in extreme cases, dirty hockey equipment can be a habitat for the hepatitis B virus, which causes very high fever, weakness and jaundice. The virus is found in infected blood and other bodily fluids, such as sweat and saliva. " It's disgusting," Dr. Dworkin said of what can lurk in a stinky hockey bag. Having dirty sports equipment, he said, "is no different than not following routine hygiene like changing your socks and underwear." Bacteria- and viral-contaminated equipment is a very easy means of transmitting infection. People who play sports are particularly susceptible to infections for various reasons: Germs grow when athletic equipment gets warm and moist; sweating softens the skin's main barrier, the stratum corneum, to the body; and germs enter the body from scrapes, cuts and bruises. Professional hockey players, who are covered from head to toe in protective padding and sweat profusely during play, can be very susceptible to infection because many, for superstitious reasons, refuse to update their equipment. But at least professionals, and players through the junior and university ranks, have training staffs responsible for the maintenance of equipment. It's those who play at the minor levels, children and beer-leaguers, who may have the most to worry about if they just leave their wet equipment in their hockey bags until it's time to play again. Not hanging up wet, smelly equipment to dry is a major reason for severe bacterial contamination. While some may wash their jerseys, hockey socks and undergarments before the next game, leaving the rest of the stuff in the bag, like Boswell does, is not uncommon. There doesn't seem to be a reasonable explanation from those who let their equipment rot, other than offering the frequent refrain, "It's kind of a guy thing." Allowing equipment to dry kills a lot of bacteria, although Dr. Dworkin suggested that cleaning equipment with disinfectants should also be part of the process, to make sure you're getting more bacteria and any spores left by dead germs. Because they're reproductive cells, spores can be activated by sweat or other moist conditions, which leads back to bacterial growth. Athletic equipment is a very good host for germs because of the plastics and foam used in its construction. For example, bacteria can get trapped in crevices and pores of the materials and, if equipment isn't dried or cleaned properly, the germs can flourish, multiplying en masse. It is highly recommended that players do not share any piece of equipment. Health issues are not the only problem with dirty equipment. " What (damages) equipment is bacteria and mould buildup," said Darren McCready, co-owner of Hockey Wash, a local company that specializes in cleaning sports gear in what basically is a huge washing and drying machine that uses special detergents and sanitizers. " (Dirty equipment) eventually rots and falls apart. Equipment is expensive. By keeping it clean, you're protecting your investment." Skora's lab, which primarily conducts microbiological tests for bacteria in wells, air, restaurants and food-processing plants, took bacteria samples from five-by-five-centimetre surfaces of eight pieces of Boswell's equipment -- helmet, shoulder pads, pants, skates, elbow pads, athletic support, gloves and shin pads. A count of 25 or less of bacteria on hard surfaces (such as a restaurant counter) is considered acceptable under Quebec provincial guidelines. Anything above is considered a potential health hazard and disinfection is recommended. There are no guidelines to bacteria levels in hockey equipment, although Skora said the levels in Boswell's equipment were simply too high to ignore out of concern for infection. Here's what the lab results show: 1. Shoulder pads: 480 bacteria that were reproducing on that equipment as we spoke. A concentration of 19 times higher than the acceptable quota under the provincial guidelines. 2. Helmet: 750 (30 times higher) 3. Skates: 2,800 (112 times higher) 4. Pants: 4,500 (180 times higher) 5. Elbow pads: 6,200 (248 times higher) 6. Athletic support: 9,400 (376 times higher) 7. Gloves: 79,000 (3,160 times higher) 8. Shins pads: 86,000 (3,440 times higher) In other words, in Boswell's equipment, the lab found 188,650 living, reproducing bacteria on just eight samples, measuring 25 square centimetres each. How many more were there? Three, four million? Boswell's equipment has since been cleaned by Hockey Wash. Micro B tested the equipment afterward, and Skora says the results were amazing compared with the first tests. Every sample taken showed counts of bacteria to be within the standard set by Quebec's environment ministry for hard surfaces -- 25 or less. There was no sample taken in the second test of Boswell's skates: he didn't want them cleaned for fear that the slightest change after being washed might throw off his game. Here are the result from the second lab test: 1. Shoulder pads: 18 2. Helmet: 22 3. Skates: No sample taken. 4. Pants: 24 5. Elbow pads: 14 6. Athletic support: 8 7. Gloves: 16 8. Shin pads: 12 While your skin is already a host to some of the bacteria found in the contents of a hockey bag, and some of that bacteria on your skin is considered "good" because it kills harmful germs, Dr. Dworkin said the "bacterial load on dirty hockey equipment is greater than what your body is used to." Thus, bacteria and viruses that get into your system, or that of the player you just made contact with, can make either one of you as sick as a dog or cause some excruciating pain. Dr. Dworkin explained there are numerous ways for players to suffer or pass ailments caused by the bacteria and viruses. Most of it, he said, is through hand-to-hand contact. One example is a player who adjusts a piece of equipment, such as his shoulder pads or athletic support, and then grabs a drink from a water bottle. Another player touches the same water bottle, either to move it or take a drink, and then adjusts his mouthguard, allowing the bacteria he picked up from the bottle to mix with his saliva, which carries it into his body. Players colliding on the ice can send contaminated sweat showering into the air, and into the nasal or oral passages. Skin infections occur as bacteria find their way under the skin through cuts, abrasions and bruises. Germs also get under the skin as it gets soft and prune-like from the body's heat and sweat. Fungal infections such as athlete's foot also require heat and moisture to be stimulated. Dr. Dworkin said various micro-organisms can cause problems once they get through the skin because they multiply rapidly in warm and wet cells. Nasty illnesses that bacteria and viruses found in hockey equipment can cause include: * Gastroenteritis (commonly know as stomach flu, which results in diarrhea and nausea); * Other viral illnesses such as influenza, colds, pneumonia and chicken pox; * Various skin infections, including impetigo, caused by either the streptococcus (strep) or staphylococcus (staph) germs; * Diarrhea, bleeding and cramping, caused by a strain of E. coli, found in fecal matter and often ending up in the athletic support. The streptococcus and staphylococcus families of bacteria can be extremely dangerous and are spread through broken skin. Staphylococcus aureas, or MRSA, is one that is particularly feared because it is resistant to certain antibiotics, can poison blood and even kill you. Sometimes, though, it causes no more than a mildly painful blister. Recent cases of MRSA, considered a "superbug," have involved U.S. high school and university football players who developed infections through razor nicks from cosmetic body shaving. The infections spread through body contact. Last year, several members of the NFL's Houston Texans developed MRSA infections and needed intravenous antibiotics. Former Toronto Maple Leafs forward Mikael Renberg had a run-in with group-A strep and nearly lost a hand as a result. While tying his skates for a practice in late December 2002, a lace opened a blister on his left hand. The hand became so infected the next day that he developed a 104-degree fever and ended up in a Vancouver hospital, where doctors considered amputation over fears that the infection could spread and kill him. Boston Bruins star Joe Thornton was put on intravenous antibiotics in January 2003, after he fell and bruised his left elbow during practice and developed an infection a few days later. It was believed that the infection came from bacteria in his elbow pad or from bacteria in his hand, which he transmitted by rubbing the bruise. Some other NHL players who suffered bad infections in recent years include Detroit Red Wings forward Darren McCarty (elbow), Leafs goalie Eddie Belfour (hand) and former San Jose Sharks defenceman Gary Suter (shoulder). Suter's infection ate a large part of one of the triceps muscle in his upper arm. In September 2003, Tampa Bay Lightning star Vincent Lecavalier was prescribed antibiotics after his right ankle became infected through scar tissue as he was breaking in a pair of skates. Boswell? He claims he is as "healthy as a horse" and doubts he has ever suffered an illness related to his equipment.

Reprinted with the permission of the Ottawa Citizen

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Germ Warfare - No Sweat

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Clouds of Secrecy: The Army’s Germ Warfare Tests Over …

Posted: September 8, 2016 at 6:49 am

Format: Paperback

This book contains shocking but carefully documented details about germ warfare tests conducted by the U.S. Army in the 1960s. It is an eye opener about a range of Army experiments that exposed millions of Americans to various bacteria without their knowledge. The purpose supposedly was to see how vulnerable Americans would be to a germ attack. The book is clearly written and provides riveting descriptions of many of the tests. The most amazing thing about the tests was the number of American cities and their populations that were targeted. They included New York City, San Francisco, St. Louis and hundreds of other cities and towns. The germs were not true warfare agents like anthrax, but they apparently caused several people to become sick, some perhaps fatally. In the current climate of fear about terrorism, Clouds of Secrecy provides an invaluable reminder that secret government actions intended to protect the public may themselves create risks to its safety.

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Germ Warfare Against America: Part I What Is Gulf War …

Posted: August 21, 2016 at 11:18 am

by Donald S. McAlvaney, Editor, McAlvaney Intelligence Advisor (MIA), August 1996

GWI is a communicable, moderately contagious and potentially lethal disease, resulting from a laboratory modified germ warfare agent called Mycoplasma fermentans (incognitus). [ED. NOTE: There were actually up to 15 such agents used in Desert Storm by Iraq only three have been identified at this writing: mycoplasma fermentans (incognitus), mycoplasma genitalia, and Brucella species.]. Myco- plasma fermentans (incognitus) is a biological which contains most of the (HIV) envelope gene, which was most likely inserted into it in germ warfare laboratories.

GWI spreads far more easily than AIDS, by sex, by casual contact, through perspiration, or by being close to someone who coughs. Your children can be infected at a playground or school. The Nicolsons, who have isolated the micro-organisms, say that it is airborne and moderately contagious.

Joyce Riley had an American Legion chapter leader call her in mid-95 who said, I was visiting the Desert Stormers at the VA Hospital and after two weeks I had the same illness they did just from visiting them at the VA. It sounds almost like tuberculosis-type contagion.

To illustrate the moderately contagious nature of the biologicals Saddam used, Dr. Garth Nicolson cited the case of a young woman who served in a transportation squad who contracted GWI while assigned to a graves registration unit during the hostilities. She is currently the sole survivor of the 16 members of her unit.

She has severe GWI, is partially paralyzed, has multiple chemical sensitiveness (which complicate treatment) and has the mycoplasmic infection. All of the other 15 members of her unit are dead from what we suspect were infectious diseases. These (graves registration) units had to deal with the registration and disposal of thousands of dead Iraqi soldiers who were, we strongly suspect, exposed to GWI.

GWI is the direct health consequence of prolonged exposure to low (non-lethal at the time of exposure) levels of chemical and biological agents released primarily by direct Iraqi attack via missiles, rockets, artillery, or aircraft munitions, and by fallout from allied bombings of Iraqi chemical warfare munitions facilities during the 38-day war.

The effects of these exposures were exacerbated by the harmful and synergistic side effects of unproven (untested) pyridostigmine bromide (PB) pills (nerve agent pre-treatment pills) forcibly administered to our troops; botulinum toxoid vaccines (also untested and experimental) forcibly administered to our troops; anthrax vaccines and several other experimental vaccines, all forcibly administered to our troops like so many laboratory guinea pigs.

Estimates of the number of vets who are sick are just that estimates. Estimates of 50 to 90,000 sick vets are now obsolete. Over 160,000 Gulf War vets have reported to the Gulf War Registry (kept by the Department of Defense which still maintains that the disease does not exist). Dr. Garth Nicolson estimates the number of veterans sick with GWI to be closer to 100,000 to 200,000 with approximately 15,000 dead. This does not include wives, children or other family members, friends or associates (secondary infectees) who are sick, disabled, dying or dead.

By August 15, 1991, 17,000 out of 100,000 reservists and National Guardsmen who served in the Gulf conflict had reported to the VA that they were ill. Four years later (in August 96) that number is likely to have tripled to 51,000, or over half of the total. Joyce Riley estimates that 1/2 of all Desert Stormers may now be positive for Mycoplasma fermentans (incognitus). Riley (and the Nicolsons) also estimate that a large percent of all GWI victims may ultimately die from the disease, or suicide.

On 7/31/96, Tony Flint, spokesperson for the British Gulf War Veterans Association, reported that the number of GW veterans deaths in U.K. is l.233 out of 51,000 Brits who participated. Of these deaths, 13% or 162 were from suicide. These are huge numbers of suicide victims who took their lives due to their lack of treatment and incredible pain levels.

Whole families are now ill. Nor do the above numbers include babies which are being born dead or severely deformed like the thalidomide babies of the 50s. Some of the baby deformities are Goldenhar syndrome, wherein babies are born with one or more limbs missing, a missing eye or other deformity. It is now estimated that a large percent of babies born to infected veterans are being born deformed or with birth problems.

The study done for former U.S. Senator Don Riegle (D-MI) concluded that 78% of wives of veterans who are sick are also likely to be sick, that 25% of their children born before the war are also likely to be sick, and that 65% of children born to sick Gulf War veterans after the war also are likely to be sick.

The Nicolsons, after listening to health complaints of many veterans of Desert Storm (including their step-daughter, then Staff Sergeant Sharron McMillan, who served with the Armys 101st Airborne Division-Air Assault, in the deep insertions into Iraq), concluded that the symptoms can be explained by aggressive, pathogenic mycoplasma and other microorganism infections.

Mycoplasmas are similar to bacteria. They are a group of small microorganisms, in between the size and complexity of cells and viruses, some of which can invade and burrow very deep into the cell and cause chromic infections. According to the Nicolsons, normal mycoplasma infections produce relatively benign diseases limited to particular tissue sites or organs, such as urinary tract or respiratory infections.

However, the types of mycoplasmas which the Nicolsons have detected in Desert Storm veterans are very pathogenic, colonize in a variety of organs and tissues, and are very difficult to treat. [ED. NOTE: The Nicolsons tested thousands of veterans blood samples (free-of-charge) while at the M.D. Anderson Center].

These mycoplasmas can be detected by a technique the Nicolsons developed called Gene Tracking, whereby the blood is separated into red and white blood cell fractions, and then further fractionated into nucleoproteins that bond to DNA, the genetic material in each cell. Finally, the purified nucleoproteins are probed to determine the presence of specific mycoplasma gene sequences. [ED. NOTE: Obviously this is no ordinary blood test and can only be understood or done by a small handful of pathologists or microbiologists in the world today].

As the Nicolsons wrote in a recent paper entitled Chronic Fatigue Illness and Desert Storm Were Biological Weapons Used Against Our Forces in the Gulf War?: In our preliminary study on a small number of Gulf War veterans and their families, we have found evidence of mycoplasmic infections in about one-half of the patients whose blood we have examined.

Not every Gulf War veteran had the same type of mycoplasma DNA sequences that came from mycoplasmas bound to or inside their white blood cells. Of particular importance, however, was our detection of highly unusual retroviral DNA sequences in the same samples by the same technique. These highly unusual DNA sequences included a portion of the HIV-1 (the AIDS-causing virus) genetic code, the HIV-1 envelope gene, but not the entire HIV-1 viral genomes.

The type of mycoplasma we identified was highly unusual and it almost certainly could not occur naturally. It has one gene from the HIV-1 virus but only one gene. This meant it was almost certainly an artificially modified microbe altered purposely by scientists to make them more pathogenic and more difficult to detect.

Thus these soldiers were not infected with the HIV-1 virus, because the virus cannot replicate with only one HIV-1 envelope gene that we detected. [ED. NOTE: But, infected soldiers do exhibit many of the symptoms of AIDS while testing HIV negative. Garth Nicolson says that Mycoplasma fermentans (incognitus) contains about 40% of the HIV virus which causes AIDS. He told this writer on 8/9/96 that some soldiers do test HIV-1 positive, but do not have the HIV virus only the envelope gene product].

Interestingly, the specific DNA sequence that we detected encodes a protein that, when expressed on the surface of the mycoplasma, would enable any myco-plasma to bind to many cell types in the body, and even enter those cells.

Thus this genetic manipulation could render a relatively benign mycoplasma much more invasive and pathogenic and capable of attacking many organ and tissue systems of the body.

Such findings suggest that the mycoplasmas that we have found in Gulf War veterans are not naturally occurring organisms, or to be more specific, they were probably genetically modified or engineered to be more invasive and pathogenic, or quite simply, more potent biological weapons.

In our rather small sample of Gulf War veterans, it seems that the soldiers that were involved in the deep insertions into Iraq and those that were near Saudi SCUD impact zones may be the ones at highest risk for contracting the mycoplasmas that we feel are a major culprit in the Desert Storm-associated chronic fatigue illness. Our preliminary research indicates that the types of mycoplasmas found in some of the Desert Storm veterans with the most severe chronic symptoms may have been altered, probably by genetic manipulation, suggesting strongly that biological weapons were used in Desert Storm.

We consider it quite likely that many of the Desert Storm veterans suffering from the symptoms (described below) may have been infected with microorganisms. Quite possibly aggressive pathogenic mycoplasmas and probably other pathogens such as pathogenic bacteria as well, and this type of multiple infection can produce the chronic symptoms even long after exposure. [ED. NOTE: Three to seven years later, Joyce Riley calls it a time-release form of illness].

[ED. NOTE: Joyce Riley and the Nicolsons believe that the microbe just described is only one of 10 to 15 different microbes or different types of germ warfare that could have been utilized].

Micotoxins are toxins that are associated with fungus. Fungi and micotoxins have long been a very secret carrier of germ warfare agents. Micotoxins are very difficult to destroy with temperature, weather, or anything else.

Mycoplasmas have for many years been studied as potential germ warfare agents. Add a recombinant DNA to the mycoplasma such as the HIV envelope gene, and youve got a very virulent form of disease that is going to be passed easily throughout the population.

Mycoplama fermentans (incognitus) (and the other 10 to 15 microbes the Nicolsons believe could have been used by Saddam) are easily manufactured and have been made for the past 15 years in America, Russia, Iraq, China, Israel and even in Libyas new biological (germ) warfare facilities.

One of the more ominous aspects of GWI is that the microorganism is communicable between humans and dogs and cats (and presumably other animals). Veterans pets are coming down with the GWI symptoms and dying. Remember one of the Nicolsons cats contracted it and died. So, the disease is contagious between species. As Joyce Riley has said, The fact that the disease is being transmitted from people to animals is almost unprecedented. To find an organism that can be transmitted to animals is truly frightening.

In England, a viral researcher friend says that he has treated a number of people with the human form of Mad Cow Disease which he says has many common characteristics with GWI. Remember, most of the cattle herd of England had to be destroyed because of Mad Cow Disease. The British researcher says he is presently seeing (and treating) dozens of new, never-before-seen viruses in the U.K.

There is a large list of signs and symptoms which can begin from six months to six or seven years from the time of exposure, and once they begin, can get progressively worse until the victim is partially or totally disabled, or dies. [ED. NOTE: With severe exposure to heavy doses of biologicals, the symptoms can show up in a few days]. These symptoms include (not listed in order of severity or frequency): (1) Chronic fatigue; (2) Frequent (or constant) throwing up and diarrhea; (3) Severe weight loss (wasting away) very similar to an AIDS patient; (4) Severe joint pains; (5) Headaches that dont go away; (6) Memory loss, concentration loss the brain begins to go; (7) Inability to sleep [ED. NOTE: Severe sleep disorders are one of the worst and most frequent symptoms. Victims often sleep in the day, awake at night, or dont sleep for days or weeks]; (8) A rash on the stomach, groin, back, face, arms often looks like a giant ring worm. Whole families often get the rash; (9) Lymph nodes begin to swell; (10) Nervous system problems begin to appear (Parkinson-like symptoms, numbness and tingling around the body which can degenerate into paralysis and death); (11) Night sweats; (12) Bizarre tumors many brain stem tumors; [ED. NOTE: the active duty tumor rate in the U.S. military has increased 600% since 1990, according to data obtained from the Veterans Admini-stration. This data is available from Joyce Riley at the American Gulf War Veterans Association, 3506 Highway 6 South #117, Sugarland, TX 77478-4401 (1-713-587-5437)]; (13) Bizarre personality changes (victims become violent, have wide mood swings, severe depression, they hibernate in a dark room, begin to drink heavily, use drugs, become violently angry. Denial is a major facet of the disease; (14) Cant work often go bankrupt; (15) A large number of victims (perhaps 50%) end up committing suicide. GWI victims are walking time bombs!

Many of the symptoms are similar to AIDS because they are both immuno- suppressive and attack the immune system. Most victims will have half to two-thirds of these symptoms (some more severe than others). Wives married to GWI victims are likely to get the disease via sex and other close contact, and their symptoms can even include cervical cancer, ovarian cysts, ovarian tumors, endometriosis, painful intercourse, chlamydia, and herpes (sexually transmitted diseases [STDs] but with no extra-marital sexual activity). About 90% of the wives of veterans who are sick with GWI are now complaining of these symptoms.

When Joyce Riley had the disease she had some of the above symptoms in addition to the following symptomology: (1) She felt like a part of the body (like a foot, a leg, a calf, an arm) was missing; (2) She felt like a pan of hot water had been splashed on her one side of her body burned; (3) She felt like a foot was in ice; (4) She had bone pain, muscle pain (like a cramp or charley horse that doesnt let up for weeks); (5) She had central nervous system symptoms (knife-like pain from the upper back to tailbone).

Bleeding and hemorrhaging are symptoms associated with GWI. In Ebola Zaire, the body bleeds out in about 48 hours. Ebola Riston (a variation of Ebola Zaire) takes about two years to cause death with severe bleeding. A number of Gulf War vets who have called Joyce Riley have told her that they are bleeding from every orifice of their body. And their doctors dont have a clue as to what is happening they just know they dont have long to live. [ED. NOTE: She gets dozens of calls each day].

The Ebola Riston virus is a version of the Ebola Zaire virus (which may have been laboratory produced) but it takes about two years or more to kill a victim, beginning with the onset of the symptoms, versus 48 hours for Ebola Zaire. [ED. NOTE: Readers of this report are strongly encouraged to buy and read the book, The Hot Zone and rent the movie Outbreak both of which deal with the Ebola Zaire virus. However, in the real world, Ebola did not come from an African monkey, cave or rain forest but probably from a biological warfare laboratory].

Lekoencephalopathy is similar to Mad Cow disease the brain dissolves! It is now spreading among the populace of England. 25 to 30-year-old paratroopers are now dying of lekoencephalopathy. Other symptoms of GWI include: recurring fever, menstrual disorders, stomach upsets and cramps, heart pain, kidney pain, thyroid problems, and in extreme cases, autoimmune-like disorders such as those that lead to paralysis.

Many GWI victims are getting medical diagnoses of MS (Multiple Sclerosis) or Guillian Barre Syndrome, and Amyotrophic Lateral Sclerosis (Lou Gehrings Disease), their neurological problems eventually lead to paralysis and death. Thousands of Gulf War vets are now being diagnosed as having MS when they really have GWI.

The reason for the autoimmune symptoms maybe related to the cell penetrating mycoplasmas and bacteria of GWI. When these microorganisms proliferate and leave the cell, they can take a piece of the cells membrane with it, resulting in host immune responses against the microorganisms as well as the normal parts of membrane associated with the microorganism. This type of response is called a concomitant immune response.

In August 95, researchers at the University of Glasgow released a report entitled, Neurological Dysfunction in Gulf War Syndrome, which was published in the March 96 issue of the Journal of Neurology, Neurosurgery and Psychiatry which said, The results between the two groups [Desert Storm vets and non-military control group] showed significant differences between the two groups in terms of nervous system function. The Gulf War veterans performed less well. They all displayed the classic symptoms of nerve damage.

Graves Disease (a disease of the thyroid) is another problem or symptom associated ith mycoplasma fermentans (incognitus) infection. If it settles in the wheart, then you can get a severe enlargement and necrosis (or degeneration) of the heart, and in some autopsies of GWI victims, the coroner says, their heart exploded.

The most severely affected (sickest) units in our military are the 101st Airborne, the 82nd Airborne, and the Big Red One out of Ft. Riley, Kansas, and the 3rd and 5th Special Forces.

[ED. NOTE: 99.9% of the medical doctors in America cant recognize GWI, dont believe it even exists because of the government and medical establishment saying it doesnt exist, would have no idea how to test for it and even less idea how to treat it. Most alternate medical practitioners are in the same boat although many of them would try detoxification and immune system therapy which would be helpful. These are answers (if the disease is not too far advanced) both in the tradition (mainline) medical area and in the alternate medicine field which will be discussed in Section VI below. If you or a family member reading this report are discouraged at this point, turn to Section VI on Methods of Treatment before continuing].

Life (11/95) featured a special report entitled: The Tiny Victims of Desert Storm, which described in heart-rending detail (with numerous photos) how the children of our veterans are being born with horrendous disfiguring birth defects. The article was subtitled, When our soldiers risked their lives in the Gulf, they never imagined that their children might suffer the consequences or that their country would turn its back on them.

In the months and years following Desert Storm, thousands of babies have been born to vets with horrible deformities (missing limbs, one eye, missing ears, incomplete or missing organs reminiscent of the Thalidomide babies of the 1950s but in far greater numbers. [ED. NOTE: Thalidomide was another experimental drug (administered to pregnant mothers) which went awry].

Meanwhile, the Department of Defense is working overtime to cover up the crisis with Gulf War babies, denying it exists, denying benefits or medical assistance to veterans with birth defected children, and even going so far as to censor the Life article cited above off of the Internet.

Dr. William Campbell Douglass is the editor of the Second Opinion newsletter and author of the book, Who Killed Africa (about how the World Health Organization smallpox inoculations may have triggered the AIDS epidemic in Africa). Dr. Douglass, a close friend of this writer, wrote in his January 1994 newsletter regarding Gulf War Illness: The symptoms are now having serious repercussions. Half or more of the babies born to Gulf War vets since the war have had some sort of birth defect or blood disorder.

Nation Magazine (1/95) estimates that 67% of babies being born to Gulf War vets who are ill are having serious birth problems. Over half of the babies now being born in Iraq today have deformities or major birth defects, according to reports Dr. Garth and Nancy Nicolson have received.

According to the Life Magazine article: In 1975, a landmark Swedish study concluded that low-level exposure to nerve and mustard gases could cause both chronic illness and birth defects. The Pentagon denies the presence of such chemicals during the Gulf War. [ED. NOTE: Even though over 18,000 chemical alarms sounded during the Gulf War] but the Czech and British governments say their troops detected both kinds of gas during the war. A 1994 report by the General Accounting Office says that: American soldiers were exposed to 21 potential reproductive toxicants, any of which might have harmed them or their future children.

A number of examples of babies born to Gulf War vets with devastating birth defects were cited in the Life Magazine article:

1) Kennedi Clark (Age 4) Born to Darrell (an Army paratrooper in the Gulf War) and Shona Clark. Kennedis face is grotesquely swollen sprinkled with red, knotted lumps. She was born without a thyroid. If not for daily hormone treatments, she would die. What disfigures her features, however, is another congenital condition: hemangiomas, benign tumors made of tangled red blood vessels. Since she was a few weeks old, they have been popping up all over on her eyelids, lips, etc.

(2) Lea Arnold (Age 4) Born to Richard and Lisa Arnold. Richard was a civilian helicopter mechanic (working for Lockheed) with the Armys 1st Cavalry Division during the Gulf War. Lea was born with spina bifida, a split in the backbone that causes paralysis and hydrocephalus (i.e. water on the brain). She needed surgery to remove three vertebrae. Today, she cannot move her legs or roll over. A shunt drains the fluid from her skull. Her upper body is so weak that she cannot push herself in a wheelchair on carpeting. To strengthen her bones, she spends hours in a contraption that holds her upright. Just about our whole world is centered around Lea, says Lisa Arnold. Huge medical bills and the unwillingness of insurance companies to cover pre-existing conditions force the family to live in poverty in order to qualify for Medicaid.

(3) Casey Minns (Age 3) Born to Army Sgt. Brad and Marilyn Minns. Casey was born with Goldenhar Syndrome, characterized by a lopsided head and spine. His left ear is missing, his digestive tract (i.e. esophagus) was disconnected. Trying to repair his damaged organs, surgeons at Walter Reed Army Medical Center damaged his vocal chords and colon, says Brad and Marilyn. His parents feed and remove his wastes through holes in his belly. His mother Marilyn, says, Sometimes it just overwhelms me, but I try to take it one day at a time.. its made worse by people who say that Gulf War Syndrome doesnt existtheyre turning their backs on us.

(4) Michael Ayers (Died at 5 Months of Age) Born to Glenn (a battery commander in the Gulf War) and Melanie Ayers. Michael was born with a mitral-valve defect in his heart. He sweat constantly until the night h woke up screaming, his arms and legs ice-cold. he died that night of congestive heart failure. As Life Magazine wrote: After Michaels death, Melanie sealed off his bedroom; she tried to close herself off as well. But soon she began to encounter a shocking number of other parents whose post-Gulf War children had been born with abnormalities. All of them were desperate to know what had gone wrong and whether they would ever again be able to bear healthy babies. With Kim Sullivan, an artillery captains wife whose infant son, Matthew, had died of a rare liver cancer, Melanie founded an informal network of fellow sufferers. Kim is here. So is Connie Hanson, wife of an Army sergeant her son, Jayce, was born with multiple deformities. Army Sgt. John Mabus has brought along his babies Zachary and Andrew who suffer from an incomplete fusion of the skull. The people in this room have turned to one another because they can no longer rely upon the military.

(5) Cedrick Miller (Age 4) Born to Steve (a former Army medic in the Gulf War) and Bianca Miller. Cedrick was born with his trachea and esophagus fused; despite surgery, his inability to hold down solid food has kept his weight to 20 pounds. His internal problems include hydrocephalus and a heart in the wrong place. Cedrick suffers, like Casey Minns, from Goldenhars Syndrome. The left half of his face is shrunken, with a missing ear and blind eye.

(6) Jayce Hanson (Age 4) Born to Paul (a Gulf War vet) and Connie Hanson. Jayce was born with hands and feet attached to twisted stumps. He also had a hole in his heart, a hemophilia-like blood condition, and underdeveloped ear canals ..a cherubic, rambunctious blond, hes the unofficial poster boy of the Gulf War babies seen by millions in People Magazine. But since his last major public appearance, he has undergone a change. His lower legs are missing. Doctors recently amputated his legs at the knees to make it easier to fit him with prosthetics. Hell say once in a while, My feet are gone, says his mother Connie, but he has been a real trooper.

(7) Alexander Albuck (Age 3) Born to Lieutenant and Kelli Albuck after two miscarriages. Alexander was born with underdeveloped lungs, Strep B infection, spinal meningitis, cranial hemorrhage, collapsed heart valve, calcium deposits in the kidneys, bleeding ulcers, cerebral palsy, vision and hearing impairments, bronchia pulmonary dysphasia, etc. Having exhausted the lifetime limit on their health insurance in the first three months, the Albucks because responsible for paying for his treatment. The first bill they received was for $154,319!

There are thousands of young children like Kennedi, Lea, Casey, Michael, Cedrick, Jayce, and Alexander (the tiny victims of Desert Storm) who have been born to Gulf War vets with horrible birth defects or who have died from these deformities. The government (especially the Defense Department) denies that the problem exists and no government medical or financial assistance is forthcoming unless a parent is still in the military (and over 2/3 of the Gulf War vets have been separated from duty since Operation Desert Storm).

As Life wrote: For parents of these children, the going is grim. They are denied insurance coverage for pre-existing conditions. They are being driven into poverty. Some join the welfare line so Medicaid will help with the impossible burden. You could be a millionaire, and there is no way you could take care of one of these children, says Lisa Arnold.

Because the U.S. government and military will not help, a Gulf War Baby Registry has been formed (in Orlando, Florida) by Dr. Betty Bekdeci to track as best as possible the birth defected children. Call 1-800-313-2232 for more information.

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Germ Warfare Against America: Part I What Is Gulf War ...

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"M*A*S*H" Germ Warfare (TV Episode 1972) – IMDb

Posted: July 29, 2016 at 3:19 am

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Pai, a severely injured North Korean POW is taking up a valuable bed in Post-Op and Pai requires AB- blood, the rarest type of blood in both Caucasians and Asians. So, naturally Frank wants to ship off Pai to the POW section. Pai is Hawkeye's patient; and Hawkeye will not release Pai. But, the whole 4077 Post-Op situation is dire and Henry takes Frank's side; and the guys tell Henry he is turning into a real Army clown. (Cue M*A*S*H, the movie.) Ruefully, Henry has to acknowledge their censure and he tells Trapper and Hawkeye to care for Pai for as long as they want, but to keep Frank (aka Mrs. Henry Blake in Army drag) OFF Henry's back. With Pai a guest I n The Swamp in Hawkeye's cot, the next issue is blood: Radar scours 4077 personnel records to find their rare blood donor. Poor Frank has a dream he is a giant soda with a big straw sticking out of him! When Pai takes a turn for the worse, the original Swamp Rats, Radar and the crew work overtime to keep one Major Montague from ... Written by LA-Lawyer

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"M*A*S*H" Germ Warfare (TV Episode 1972) - IMDb

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Articles about Germ Warfare – latimes

Posted: July 14, 2016 at 4:37 pm

NEWS

August 6, 1997 | From Reuters

Iraq could reassemble its germ warfare program within six months with a still-intact scientific team working with freeze-dried organisms, a former U.N. investigator said in a report published Tuesday. "The work force of more than 200 persons who staffed Iraq's biological warfare program is intact," Raymond Zilinskas said. "Iraq's civilian biotechnological infrastructure, comprising more than 80 research, development and production facilities, is whole and well equipped," he added.

NEWS

December 8, 2001 | From Times Wire Services

An international conference on germ warfare disbanded in chaos and anger Friday after the United States sought to cut off discussions about enforcing the 1972 Biological Weapons Convention. The treaty, ratified by the U.S. and 143 other governments, bans the development, stockpiling and production of germ warfare agents--but it has no enforcement mechanism. The purpose of the conference was to discuss the progress of a six-year effort to negotiate measures to enforce compliance.

NEWS

May 4, 1988 | JOHN M. BRODER, Times Staff Writer

Ten nations, many of them hostile to the United States, currently are producing biological weapons, making it crucial that the Army pursue its controversial plan to build a germ warfare facility in Utah, a senior Defense Department official told Congress Tuesday.

CALIFORNIA | LOCAL

January 22, 2008 | DANA PARSONS

They say war is hell, but getting sick is no picnic either. Here's my briefing: Two weeks ago I was bivouacked on the sofa around 2200 hours, eating Jell-O pudding, when I detected the first sign of hostile troop movement. Unfortunately, the invaders' advance party was small and stealthy, and my sentries paid little heed. I finished the pudding, watched more TV and went to bed around midnight. As I slept, the enemy massed. By daybreak, I was surrounded.

CALIFORNIA | LOCAL

September 6, 2002 | REBECCA TROUNSON, TIMES STAFF WRITER

Sheldon H. Harris, a Cal State Northridge historian whose groundbreaking work helped establish that Japan conducted biological warfare experiments on Chinese civilians and military prisoners during World War II, has died. He was 74. Harris died of a blood infection Aug. 31 at UCLA Medical Center, but lived long enough to experience a moment of particular gratification, his son, David, said.

CALIFORNIA | LOCAL

October 10, 2001 | ARIANNA HUFFINGTON, Arianna Huffington is a syndicated columnist. E-mail: arianna@ariannaonline.com

When it comes to matters of the heart, we've been sold the premise that men are from Mars, women are from Venus. Maybe, maybe not. But when it comes to thinking the unthinkable, the sexes are most definitely from different planets. At a dinner party in Los Angeles last week, six men and six women sat around a beautifully laid-out table. While the setting evoked an escapist fantasy, the conversation dwelt on the inescapable realities of the moment.

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Articles about Germ Warfare - latimes

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Coconut Oil: Germ Warfare! | Underground Wellness

Posted: July 5, 2016 at 11:50 pm

by Sean Croxton

It happened!

There is one particular day I look forward to each year and it went down yesterday.

I woke up, strolled to the kitchen, and found my jar of coconut oil smiling at me.

It was so beautiful, like a butterfly emerging from its cocoon to take its first flight. Like a wayward child coming home again.

It happened.

The coconut oil was liquid.

Summer is here.

Not only is the oil of all oils heart-healthy. Not only does it make your skin look dead sexy. Not only does it fight the bugs that attack your body, as we will discuss today.

Coconut oil makes one heck of a weather forecaster, too.

Yesterday brought blue skies with a high of 81 degrees in San Diego. And I didnt need the weather girl to tell me that.

The coconut oil told me.

And best of all, I can drink it from the jar now. I take my coconut oil to the head! Spoons are for wussies.

Anyway, just thought Id share in my summer excitement before dropping some knowledge bombs on you about coconut oil and your immunity. If youre on the East Coast, youve got something to look forward to in the coming weeks. Leave your jar on the counter and tweet me when your butterfly hatches!

**********************************

Tonight, its on like Donkey Kong. Bruce Fife, author of The Coconut Oil Miracle is on the UW Radio Show. Certain to be another hot one. My coconut oil told me so.

Dont miss it! 5pm PT/8pm ET

A major topic Bruce and I will be covering is the use of coconut oil as a means of fighting nasty bugs like bacteria, viruses, parasites, and yeast. One thing that dawned on me while reading his book is the well-known fact that traveling to tropical climates puts those of us from more moderate temperatures at risk of coming home with a bad case of the gut bugs.

Working with clients, one of the red flags I would see quite often was digestive dysfunction originating during or after a trip to some island paradise. For many, a stool test revealed a parasitic infection that likely lingered for years, even decades.

But what about the natives who have actually lived in these literal breeding grounds for microbes and critters for generations? Why dont they have an epidemic of digestive challenges and parasitic infection?

Its the coconut oil, baby.

When you really think about it, its quite the coincidence that God, Mother Nature, or the aliens (whoever you believe put us here) just so happened to supply one of the most antibacterial, antiviral, anti-parasitic foods on Earth to a people living in a place where such microbes flourish. Even Weston Price was amazed by the low incidence of malaria in tropical people.

Amazingly, science has yet to explain a genetic explanation for such resistance. Why not?

Because its the coconut oil, baby!

Duh!

When we feel a cold coming on, most of us should be reaching for the kitchen cabinet before the medicine cabinet. Actually, we should be taking our coconut oil to the head every day or at least using it for cooking as a means of preventing all types of nasty infections.

In last weeks blog, I typed about the medium-chain fatty acids (MCFAs) coconut oil consists of. These MCFAs, which include caprylic acid, capric acid, mystiric acid, and lauric acid, are quite sparse in our food supply. Not only are these fats burned immediately for fuel (as discussed last time), but they also possess incredible antimicrobial properties, with lauric acid having the greatest antiviral activity.

As you know, medical doctor are notorious for prescribing antibiotics for viral infections. This brings about two problems. The first problem is the ever-growing development of superbugs, which are antibiotic resistant (but maybe not MCFA-resistant). And of course, the second problem is the fact that antibiotics do not kill viruses!

But coconut oil and its MCFAs can.

Bacteria and viruses are typically coated with a lipid (fat) membrane (rhinovirus is an exception), which encloses their DNA and other cellular materials. This membrane is very fluid, flexible, and mobile, allowing it to squeeze its way in and out of tight spots.

Due to the fact that the fats making up this membrane are very similar to MCFAs, the medium-chain fatty acids from coconut can sneak past security and become absorbed into the membrane, where they weaken it, split it open, and kill it by pretty much ripping its insides out.

Coconut oil has a violent streak.

So gangsta.

The most intriguing part of this germ warfare is that the MCFAs are selective. Friendly fire isnt a problem. In the case of bacteria, we possess both good and bad bacteria in our guts. The MCFAs actually single out the bad guys and leave the good guys alone.

Its really amazing stuff.

Published research shows that the MCFAs from coconut oil can kill bacteria, viruses, fungi, and parasites that cause the following illnesses. This is just a short list. More can be found on page 77 of The Coconut Oil Miracle. Of course, MCFAs are no panacea. But they deserve far more attention in the prevention and treatment of many diseases and conditions. Then again, you cant patent coconut oil and sell if for outlandish prices. So dont expect Big Pharma to run any ads for it any time soon.

Bacterial Infections Throat and sinus infections Urinary tract infections Dental cavities and gum disease Helicobacter Pylori Gastric ulcers Ear infections Food poisoning

Viral Infections Influenza Measles Herpes Chronic fatigue syndrome AIDS and HIV

Fungal Infections Ringworm Athletes foot Candidiasis Toenail fungus

Parasite Infections Giardia

I can go on and on about the benefits of coconut oil. But Im out of time today. Gotta edit Episode 3 of the Underground Wellness Show (guest: Mark Sisson).

Dont forget to tune in to tonights UW Radio show and find out how much coconut oil you should be consuming and MORE!

Its at 5pm PT/8pm ET. Dial 347-237-5608 to ask Bruce your burning coconut questions. Or tweet me at @ugwellness.

UPDATE: Listen to the show with Dr. Fife below!

Peace.

Sean Author, The Dark Side of Fat Loss

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Coconut Oil: Germ Warfare! | Underground Wellness

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Coconut Oil: Germ Warfare! | Underground Wellness

Posted: July 3, 2016 at 6:46 pm

by Sean Croxton

It happened!

There is one particular day I look forward to each year and it went down yesterday.

I woke up, strolled to the kitchen, and found my jar of coconut oil smiling at me.

It was so beautiful, like a butterfly emerging from its cocoon to take its first flight. Like a wayward child coming home again.

It happened.

The coconut oil was liquid.

Summer is here.

Not only is the oil of all oils heart-healthy. Not only does it make your skin look dead sexy. Not only does it fight the bugs that attack your body, as we will discuss today.

Coconut oil makes one heck of a weather forecaster, too.

Yesterday brought blue skies with a high of 81 degrees in San Diego. And I didnt need the weather girl to tell me that.

The coconut oil told me.

And best of all, I can drink it from the jar now. I take my coconut oil to the head! Spoons are for wussies.

Anyway, just thought Id share in my summer excitement before dropping some knowledge bombs on you about coconut oil and your immunity. If youre on the East Coast, youve got something to look forward to in the coming weeks. Leave your jar on the counter and tweet me when your butterfly hatches!

**********************************

Tonight, its on like Donkey Kong. Bruce Fife, author of The Coconut Oil Miracle is on the UW Radio Show. Certain to be another hot one. My coconut oil told me so.

Dont miss it! 5pm PT/8pm ET

A major topic Bruce and I will be covering is the use of coconut oil as a means of fighting nasty bugs like bacteria, viruses, parasites, and yeast. One thing that dawned on me while reading his book is the well-known fact that traveling to tropical climates puts those of us from more moderate temperatures at risk of coming home with a bad case of the gut bugs.

Working with clients, one of the red flags I would see quite often was digestive dysfunction originating during or after a trip to some island paradise. For many, a stool test revealed a parasitic infection that likely lingered for years, even decades.

But what about the natives who have actually lived in these literal breeding grounds for microbes and critters for generations? Why dont they have an epidemic of digestive challenges and parasitic infection?

Its the coconut oil, baby.

When you really think about it, its quite the coincidence that God, Mother Nature, or the aliens (whoever you believe put us here) just so happened to supply one of the most antibacterial, antiviral, anti-parasitic foods on Earth to a people living in a place where such microbes flourish. Even Weston Price was amazed by the low incidence of malaria in tropical people.

Amazingly, science has yet to explain a genetic explanation for such resistance. Why not?

Because its the coconut oil, baby!

Duh!

When we feel a cold coming on, most of us should be reaching for the kitchen cabinet before the medicine cabinet. Actually, we should be taking our coconut oil to the head every day or at least using it for cooking as a means of preventing all types of nasty infections.

In last weeks blog, I typed about the medium-chain fatty acids (MCFAs) coconut oil consists of. These MCFAs, which include caprylic acid, capric acid, mystiric acid, and lauric acid, are quite sparse in our food supply. Not only are these fats burned immediately for fuel (as discussed last time), but they also possess incredible antimicrobial properties, with lauric acid having the greatest antiviral activity.

As you know, medical doctor are notorious for prescribing antibiotics for viral infections. This brings about two problems. The first problem is the ever-growing development of superbugs, which are antibiotic resistant (but maybe not MCFA-resistant). And of course, the second problem is the fact that antibiotics do not kill viruses!

But coconut oil and its MCFAs can.

Bacteria and viruses are typically coated with a lipid (fat) membrane (rhinovirus is an exception), which encloses their DNA and other cellular materials. This membrane is very fluid, flexible, and mobile, allowing it to squeeze its way in and out of tight spots.

Due to the fact that the fats making up this membrane are very similar to MCFAs, the medium-chain fatty acids from coconut can sneak past security and become absorbed into the membrane, where they weaken it, split it open, and kill it by pretty much ripping its insides out.

Coconut oil has a violent streak.

So gangsta.

The most intriguing part of this germ warfare is that the MCFAs are selective. Friendly fire isnt a problem. In the case of bacteria, we possess both good and bad bacteria in our guts. The MCFAs actually single out the bad guys and leave the good guys alone.

Its really amazing stuff.

Published research shows that the MCFAs from coconut oil can kill bacteria, viruses, fungi, and parasites that cause the following illnesses. This is just a short list. More can be found on page 77 of The Coconut Oil Miracle. Of course, MCFAs are no panacea. But they deserve far more attention in the prevention and treatment of many diseases and conditions. Then again, you cant patent coconut oil and sell if for outlandish prices. So dont expect Big Pharma to run any ads for it any time soon.

Bacterial Infections Throat and sinus infections Urinary tract infections Dental cavities and gum disease Helicobacter Pylori Gastric ulcers Ear infections Food poisoning

Viral Infections Influenza Measles Herpes Chronic fatigue syndrome AIDS and HIV

Fungal Infections Ringworm Athletes foot Candidiasis Toenail fungus

Parasite Infections Giardia

I can go on and on about the benefits of coconut oil. But Im out of time today. Gotta edit Episode 3 of the Underground Wellness Show (guest: Mark Sisson).

Dont forget to tune in to tonights UW Radio show and find out how much coconut oil you should be consuming and MORE!

Its at 5pm PT/8pm ET. Dial 347-237-5608 to ask Bruce your burning coconut questions. Or tweet me at @ugwellness.

UPDATE: Listen to the show with Dr. Fife below!

Peace.

Sean Author, The Dark Side of Fat Loss

Continued here:

Coconut Oil: Germ Warfare! | Underground Wellness

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Colloidal Silver and Biological (Germ) Warfare

Posted: June 30, 2016 at 3:45 am

Our country recently passed the 9th anniversary of the 9-11 terrorist attacks of 2001, and the subsequent terrorist anthrax mailings that resulted in the deaths of five Americans and the infection of 17 others.

And while we all might rightfully wish to forget those horrific events except for a passing prayer for the victims and their families -- and go on about our business as if nothing had ever happened

a prudent person would also quietly make sure he (or she) has taken at least a few protective precautions for their family, in case something like this ever happens again.

Crazy World

After all, you dont need me to tell you that today we live in a crazy, volatile and sometimes very scary world.

Only a few short days ago, half the Arab world erupted into fits of violent anger when a controversial preacher from Florida threatened to burn a copy of the Koran in protest of the building of the proposed Cordoba Mosque near Ground Zero 9-11 attacks.

We have homegrown terrorists, too. And you just never know when some of our countrys older enemies like Russia or China, or that lunatic midget running North Korea might decide the time is ripe again to try to bring America to her knees.

The bottom line is that today, I dont think anyone in the U.S. lives in an it cant happen here fantasy world any longer. We all know it can happen here. And that it can take very little to set it off.

Therefore, after reflecting on these facts, I thought it might be high-time to revisit the idea of using colloidal silver as a means of protecting ourselves and our family members during a terrorist germ warfare attack.

A Quick Look at the Idea of Using Colloidal Silver

Against Germ Warfare Pathogens!

Will colloidal silver really work against germ warfare (i.e., biological warfare) agents like anthrax?

The truth of the matter is that while germ warfare experts might know the answer to that question, theyre not telling.

After all, our country also has a huge arsenal of germ warfare agents. And as you can probably imagine, we wouldnt necessarily want our enemies to know the antidote if one existed particularly if it was as easy to make and distribute as colloidal silver.

Nevertheless, we do have some strong indications that colloidal silver may very well be a valid first-line-of-defense against germ warfare pathogens.

So lets take a quick look at a little bit of history, and some of the known facts about colloidal silver, and see if we can make a reasonable assumption as to whether or not colloidal silver might serve as a potent natural remedy against germ warfare agents.

Colloidal Silver and the Soviet Military

Author Mark Aarons discusses the idea of colloidal silvers potential effectiveness against germ warfare pathogens in his 1994 book, The Secret War Against the Jews:

There is little defense against [a biological germ warfare] attack, and what few antidotes exist are withheld from the public as military secrets.

One of the best examples of this is Movidyn, a substance that the Soviets discovered in their satellite state of Czechoslovakia way back in the 1950s.

Movidyn is a form of colloidal silver, odorless, tasteless, and cheaper to produce than chlorine disinfectants. One part per billion of powdered Movidyn in water has a germicidal effect.

In a study of infected wells, it completely destroyed typhus, malaria, cholera, and amoebic dysentery. Drinking containers washed in Movidyn retained their germ-fighting abilities for several weeks.

Movidyn seems to be a cost-effective prophylactic for most of the water-borne diseases that infect the Third World.

To the astonishment of the Soviet military, Movidyn also disinfected every germ warfare bacteria in the Soviet arsenal, even their newest designer poisons.

In other words, Movidyn was too good.

The Czech factory was disassembled and carted back to the Soviet Union. To this day, the Movidyn formula seems to have been suppressed from the world.

-- Mark Aarons, The Secret War Against the Jews, 1994, pages 293-294

Microbiologist Larry Wayne Harris

On Colloidal Silver and Germ Warfare

In the most recently revised edition of my 547-page book, The Ultimate Colloidal Silver Manual, I also discuss the very real possibility that colloidal silver will turn out to be a valid defense against germ warfare agents during a terrorist biological attack

at least, for those who are prepared in advance and have plenty of colloidal silver stocked up, or who are foresighted enough to own the means of colloidal silver production so they can make their own colloidal silver whenever needed.

Heres what I wrote:

When former CIA microbiologist Larry Wayne Harris was asked on national television whether there were any natural substances that could protect the population against anthrax and other germ warfare agents, he responded:

The only natural substance I know of that is effective against these microbes is colloidal silver. I tested that myself when I was with the CIA, and found it effective against both anthrax and the bubonic plague pathogens.

After leaving the CIA, microbiologist Larry Harris is said to have re-tested colloidal silver against anthrax in his private laboratory in1997, and again found it to be highly effective.

According to Harris confidant Mike Seiler:

Harris definitely confirmed colloidal silver kills the anthrax pathogen. He used the minimum inhibitory test, in which he took ten vials of anthrax and put correspondingly higher concentrations of colloidal silver in each vial until he determined which concentration gives an effective kill rate. Harris discovered the kill rate was at 100 parts per billion an amazingly small amount of colloidal silver.

It is also important to note that colloidal silver was one of the few substances on earth that was successfully used against anthrax and other plague-like pathogens in the early 1900s prior to the advent of modern-day prescription antibiotic drugs, as verified by the 1919 book Colloids in Biology and Medicine by H. Beckhold, pages 364-376.

In fact, according to researcher James South, M.A., as early as 1887 a number of researchers had discovered that silver both in liquid solution and as an airborne aerosol was toxic to deadly anthrax spores. [Ref: N. Grier, Silver and Its Compounds in Disinfection, Sterilization and Preservation, S. Block, ed., Philadelphia: Lea & Febiger, 1983, pages 380-428; H. Bechold, Colloids in Biology and Medicine, N.Y.,: D. Van Nostrand, 1919, pages 364-376; Anti-Aging Bulletin, International Antiaging Systems, Vol. 4, Issue 3. Apr/May, 1999, Hi Yo Silver, Away! by James South, M.A.]

Considering that anthrax is said to be the all-time favorite biological warfare agent of Islamic terrorists and is one of the infectious biological agents intelligence experts claim terrorist cell teams are known to be in possession of it would seem to be a prudent precaution indeed to have the ability to make your own therapeutic-quality colloidal silver at home in order to help protect yourself and your family in the event of a terrorist biological attack on U.S. cities.

-- from The Ultimate Colloidal Silver Manual, 2009, pages 313-314

The above chapter goes on to discuss theoretical dosage levels of colloidal silver for use against germ warfare pathogens.

Later in the above chapter, I also quote microbiologist
Larry Wayne Harris as saying that in order for colloidal silver to be effective during a germ warfare attack, youll need to have certain levels of colloidal silver already built up in your bloodstream, cells and tissues, well before a terror attack occurs. Harris stated:

In the event of outbreaks of biological plagues, those who have already been taking sufficient levels of colloidal silver will have an automatic resistance in their bodies

If, however, a person has not been taking colloidal silver for 30 to 50 days prior to exposure to a plague, silver will have little effect. This is because invading bacteria can kill within several days, while it takes weeks for colloidal silver to be spread through your entire bodys millions of cells.

I don't know about you. But for me, the idea that colloidal silver would only work during a germ warfare attack if you've already been using it daily for one to two months before being exposed to germ warfare agents, is not a very appealing one.

After all, many people who are experienced in colloidal silver usage only use it periodically -- for example, if they feel a cold coming on, or whenever theyve actually come down with an infection and they want to deal with it naturally.

Is There Some Other Way To Get

Colloidal Silver Into the Body, Quickly and Effectively?

Fortunately, there is a way to get colloidal silver into the bloodstream and the bodys cells and tissues quickly and easily.

And we have the prestigious Health Sciences Institute (HSI) to thank for bringing this to our attention.

You see, HSI addressed this very topic in an e-alert to their members, back in October 2001, shortly after the 9-11 terrorist attacks and subsequent anthrax attacks on our nation.

As the HSI pointed out at the time, one of their well-known health symposium panelists, Dr. Marcial-Vega, had discovered while dealing with pneumonia patients the fact that colloidal silver can be quickly and easily carried into the human blood stream and from there into the bodys cells and tissues, simply by nebulizing it.

Nebulizing is a process by which colloidal silver is run through a small medical device called a nebulizer (inexpensively available on e-Bay) which turns the colloidal silver solution into a fine mist. This fine mist can easily be breathed into the lungs as its produced by the machine. And from the lungs the body can efficiently and effectively distribute the colloidal silver straight into the blood stream, cells and tissues.

Heres what the Health Sciences Institute told their members:

Based on his experience treating other types of bacterial lung infections, Dr. Marcial-Vega believes he has discovered a way to prevent anthrax from developing even if you've already been exposed.

He's currently talking with government health authorities about testing his hypothesis on live anthrax spores, but asked us bring this information directly to you now.

Just in his last decade of medical practice, Dr. Marcial-Vega has treated hundreds of people with a variety of viral, fungal, and bacterial pneumonias. And of all the available treatments, he has seen the greatest success with nebulizer treatments using a colloidal silver preparation.

Silver has long been known for its anti-bacterial properties, and the nebulizer allows the mineral to reach the lungs and kill harmful bacteria. Now, in the face of the anthrax threat, he believes it can do the same thing with anthrax spores.

'We are constantly filtering all kinds of bacteria through our lungs,' explained Dr. Marcial-Vega. Normally, a healthy body is able to kill off any dangerous bacteria on its own. But in the case of illness, like pneumonia, or an especially lethal bacteria like anthrax, the body may need some extra help.

For anthrax prevention, he recommends a daily nebulizer treatment with 4 cc's of colloidal silver. By following this protocol, Dr. Marcial-Vega says your body can likely kill off the anthrax spores before you even know you were exposed. Colloidal silver may even be useful to treat cutaneous anthrax with the preparation being directly applied to the affected skin.

Dr. Marcial-Vega says there are no concerns about using this treatment because colloidal silver has no toxicity and no side effects. He has used the colloidal silver nebulizer treatments on infants, the elderly, and AIDS patients with pneumonia and has seen great results. All have responded quickly to the treatment even when no other approach seemed to help, and no one reported any adverse reactions.

Nebulizers are widely used to treat asthma, and are readily available at drug stores nationwide. The cost generally runs between $50 and $120 for the machine. Each member of the family should have their own mask, and both adult and pediatric sizes are available for a few dollars each. But the entire family can share the nebulizer machine and the tubing."

If youre interested, you can read a more recent article here on using what I call a poor mans nebulizer. This is simply an inexpensive cool mist vaporizer from Wal-Mart or any other drug store. These inexpensive little devices do pretty much exactly what a medical nebulizer would do as long as you're using full-strength colloidal silver in it.

No Clinical Evidence

The bottom line is that theres no real clinical evidence for colloidal silvers potential effectiveness in humans against germ warfare agents such as anthrax and others.

Thats chiefly because no one is going to allow themselves to be infected with such deadly biological agents in order to test the colloidal silver hypothesis.

Even if they conducted animal tests to see if colloidal silver would be effective against germ warfare agents, its likely the results would be kept secret due to national security. Again, we wouldnt announce to our enemies the antidote to one of the most potent (albeit non-humanitarian) weapons in our own weapons of mass destruction arsenal.

Nevertheless, theres plenty of historical and circumstantial evidence to indicate that colloidal silver may very well be a first-line-of-defense remedy against germ warfare pathogens.

And for that reason alone its worth owning a high-quality colloidal silver generator so you can make all of the colloidal silver you could ever need, quickly and easily, any time you need it, in the comfort and privacy of your own home.

Helpful Links:

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-- Michael Cutler, M.D., Editor, Easy Health Options

-- Bob Livingston, The Bob Livingston Letter

-- Dr. Keith Scott-Mumby, M.D., MBChB, PhD, author Cancer Research Secrets, Complete Parasites Handbook, and Survive Without Antibiotics

-- Dr.
Kathleen Olsson Nelson, RN, BA, MA, PhD, PhD, FSNPM, FCH., Clinical Psychologist and Nutritional Consultant

-- Donald S. McAlvany, The McAlvany Intelligence Advisor, October 2013

-- Gary C. King, best-selling author of Blood Lust: Portrait of a Serial Killer and other true crime books and stories

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Colloidal Silver and Biological (Germ) Warfare

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History of biological warfare – Wikipedia, the free …

Posted: June 28, 2016 at 2:57 am

Various types of biological warfare (BW) have been practiced repeatedly throughout history. This has included the use of biological agents (microbes and plants) as well as the biotoxins, including venoms, derived from them.

Before the 20th century, the use of biological agents took three major forms:

In the 20th century, sophisticated bacteriological and virological techniques allowed the production of significant stockpiles of weaponized bio-agents:

The earliest documented incident of the intention to use biological weapons is recorded in Hittite texts of 15001200 BC, in which victims of tularemia were driven into enemy lands, causing an epidemic.[1] Although the Assyrians knew of ergot, a parasitic fungus of rye which produces ergotism when ingested, there is no evidence that they poisoned enemy wells with the fungus, as has been claimed.

According to Homer's epic poems about the legendary Trojan War, the Iliad and the Odyssey, spears and arrows were tipped with poison. During the First Sacred War in Greece, in about 590 BC, Athens and the Amphictionic League poisoned the water supply of the besieged town of Kirrha (near Delphi) with the toxic plant hellebore.[2] During the 4th century BC Scythian archers tipped their arrow tips with snake venom, human blood, and animal feces to cause wounds to become infected.

In a naval battle against King Eumenes of Pergamon in 184 BC, Hannibal of Carthage had clay pots filled with venomous snakes and instructed his sailors to throw them onto the decks of enemy ships.[3] The Roman commander Manius Aquillius poisoned the wells of besieged enemy cities in about 130 BC. In about AD 198, the Parthian city of Hatra (near Mosul, Iraq) repulsed the Roman army led by Septimius Severus by hurling clay pots filled with live scorpions at them.[4]

There are numerous other instances of the use of plant toxins, venoms, and other poisonous substances to create biological weapons in antiquity.[5]

The Mongol Empire established commercial and political connections between the Eastern and Western areas of the world, through the most mobile army ever seen. The armies, composed of the most rapidly moving travelers who had ever moved between the steppes of East Asia (where bubonic plague was and remains endemic among small rodents), managed to keep the chain of infection without a break until they reached, and infected, peoples and rodents who had never encountered it. The ensuing Black Death may have killed up to 25 million in China and roughly a third of the population of Europe and in the next decades, changing the course of Asian and European history.

During the Middle Ages, victims of the bubonic plague were used for biological attacks, often by flinging fomites such as infected corpses and excrement over castle walls using catapults. In 1346, during the siege of Kafa (now Feodossia, Crimea) the attacking Tartar Forces which were subjugated by the Mongol empire under Genghis Khan, used the bodies of Mongol warriors of the Golden Horde who had died of plague, as weapons. An outbreak of plague followed and the defending forces retreated, followed by the conquest of the city by the Mongols. It has been speculated that this operation may have been responsible for the advent of the Black Death in Europe. At the time, the attackers thought that the stench was enough to kill them, though it was the disease that was deadly.[6][7]

At the siege of Thun-l'vque in 1340, during the Hundred Years' War, the attackers catapulted decomposing animals into the besieged area.[8]

In 1422, during the siege of Karlstein Castle in Bohemia, Hussite attackers used catapults to throw dead (but not plague-infected) bodies and 2000 carriage-loads of dung over the walls.[9]

The last known incident of using plague corpses for biological warfare occurred in 1710, when Russian forces attacked the Swedes by flinging plague-infected corpses over the city walls of Reval (Tallinn).[10] However, during the 1785 siege of La Calle, Tunisian forces flung diseased clothing into the city.[9]

English Longbowmen usually did not draw their arrows from a quiver; rather, they stuck their arrows into the ground in front of them. This allowed them to nock the arrows faster and the dirt and soil was likely to stick to the arrowheads, thus making the wounds much more likely to become infected.

The Native American population was devastated after contact with the Old World due to the introduction of several fatal infectious diseases, notably smallpox.[11] These diseases can be traced to Eurasia where people had long lived with them and developed some immunological ability to survive their presence. Without similarly long ancestral exposure, indigenous Americans were immunologically naive and therefore extremely vulnerable.[12][13]

There are two documented instances of biological warfare by the British against North American Indians during Pontiac's Rebellion (176366). In the first, during a parley at Fort Pitt on June 24, 1763, Captain Simeon Ecuyer gave representatives of the besieging Delawares two blankets and a handkerchief enclosed in small metal boxes that had been exposed to smallpox, hoping to spread the disease to the Natives in order to end the siege. The British soldiers lied to the Natives that the blanket pieces had contained special powers.[14]William Trent, the militia commander, left records that clearly indicated that the purpose of giving the blankets was "to Convey the Smallpox to the Indians."[15]

British commander Lord Jeffrey Amherst and Swiss-British officer Colonel Henry Bouquet discussed the topic separately in the course of the same conflict; there exists correspondence referencing the idea of giving smallpox-infected blankets to enemy Indians. It cited four letters from June 29, July 13, 16 and 26th, 1763. Excerpts: Amherst wrote on July 16, 1763, "P.S. You will Do well to try to Inocculate the Indians by means of Blankets, as well as to try Every other method that can serve to Extirpate this Execrable Race. I should be very glad your Scheme for Hunting them Down by Dogs could take Effect,..." Bouquet replied on July 26, 1763, "I received yesterday your Excellency's letters of 16th with their Inclosures. The signal for Indian Messengers, and all your directions will be observed." Smallpox is highly infectious and does not require contaminated blankets to spread uncontrollably, and together with measles, influenza, chicken pox, and so on had been doing so since the arrival of Europeans and their animals. Trade and combat also provided ample opportunity for transmission of the disease. See also: Smallpox during Pontiac's Rebellion. It is unclear if the blanket attempt succeeded. It is estimated that between 400,000-500,000 Native American Indians during and after the war died from smallpox.[13][16][17]

Australian aborigines (Kooris) have always maintained that the British deliberately spread smallpox in 1789,[18] but this possibility has only been raised by historians from the 1980s when Dr Noel Butlin suggested; there are some possibilities that ... disease could have been used deliberately as an exterminating agent.[19]

In 1997, David Day claimed there remains considerable circumstantial evidence to suggest that officers other than Phillip, or perhaps convicts or soldiers deliberately spread smallpox among aborigines[20] and in 2000 Dr John Lambert argued that strong circumstantial evidence suggests the smallpox epidemic which ravaged Aborigines in 1789, may have resulted from deliberate infection.[21]

Judy Campbell argu
ed in 2002 that it is highly improbable that the First Fleet was the source of the epidemic as "smallpox had not occurred in any members of the First Fleet"; the only possible source of infection from the Fleet being exposure to variolous matter imported for the purposes of inoculation against smallpox. Campbell argued that, while there has been considerable speculation about a hypothetical exposure to the First Fleet's variolous matter, there was no evidence that Aboriginal people were ever actually exposed to it. She pointed to regular contact between fishing fleets from the Indonesia archipelago, where smallpox was endemic, and Aboriginal people in Australia's North as a more likely source for the introduction of smallpox. She notes that while these fishermen are generally referred to as Macassans, referring to the port of Macassar on the island of Sulawesi from which most of the fishermen originated, some travelled from islands as distant as New Guinea. She noted that there is little disagreement that the smallpox epidemic of the 1860s was contracted from Macassan fishermen and spread through the Aboriginal population by Aborigines fleeing outbreaks and also via their traditional social, kinship and trading networks. She argued that the 1789-90 epidemic followed the same pattern.[22]

These claims are controversial as it is argued that any smallpox virus brought to New South Wales probably would have been sterilised by heat and humidity encountered during the voyage of the First Fleet from England and incapable of biological warfare. However, in 2007, Christopher Warren demonstrated that the British smallpox may have been still viable.[23] Since then some scholars have argued that the British committed biological warfare in 1789 near their new convict settlement at Port Jackson.[24][25]

In 2013 Warren reviewed the issue and argued that smallpox did not spread across Australia before 1824 and showed that there was no smallpox at Macassar that could have caused the outbreak at Sydney. Warren, however, did not address the issue of persons who joined the Macassan fleet from other islands and from parts of Sulawesi other than the port of Macassar. Warren concluded that the British were "the most likely candidates to have released smallpox" near Sydney Cove in 1789. Warren proposed that the British had no choice as they were confronted with dire circumstances when, among other factors, they ran out of ammunition for their muskets. Warren also uses native oral tradition and the archaeology of native graves to analyse the cause and effect of the spread of smallpox in 1789.[26]

Prior to the publication of Warren's article (2013), John Carmody argued that the epidemic was an outbreak of chickenpox which took a drastic toll on an Aboriginal population without immunological resistance. With regard to smallpox, Dr Carmody said: "There is absolutely no evidence to support any of the theories and some of them are fanciful and far-fetched.." [27][28] Warren covered the chickenpox theory at endnote 3 of Smallpox at Sydney Cove - Who, When, Why?.[29]

By the turn of the 20th century, advances in microbiology had made thinking about "germ warfare" part of the zeitgeist. Jack London, in his short story '"Yah! Yah! Yah!"' (1909), described a punitive European expedition to a South Pacific island deliberately exposing the Polynesian population to measles, of which many of them died. London wrote another science fiction tale the following year, "The Unparalleled Invasion" (1910), in which the Western nations wipe out all of China with a biological attack.

During the First World War (19141918), the Empire of Germany made some early attempts at biological warfare. Those attempts were made by special sabotage group headed by Rudolf Nadolny. Using diplomatic pouches and couriers, the German General Staff supplied small teams of saboteurs in the Russian Duchy of Finland, and in the then-neutral countries of Romania, the United States, and Argentina.[citation needed] In Finland, saboteurs mounted on reindeer placed ampoules of anthrax in stables of Russian horses in 1916.[30] Anthrax was also supplied to the German military attach in Bucharest, as was glanders, which was employed against livestock destined for Allied service. German intelligence officer and US citizen Dr. Anton Casimir Dilger established a secret lab in the basement of his sister's home in Chevy Chase, Maryland, that produced glanders which was used to infect livestock in ports and inland collection points including, at least, Newport News, Norfolk, Baltimore, and New York, and probably St. Louis and Covington, Kentucky. In Argentina, German agents also employed glanders in the port of Buenos Aires and also tried to ruin wheat harvests with a destructive fungus.

The Geneva Protocol of 1925 prohibited the use of chemical weapons and biological weapons, but said nothing about experimentation, production, storage, or transfer; later treaties did cover these aspects. Twentieth-century advances in microbiology enabled the first pure-culture biological agents to be developed by World War II.

In the interwar period, little research was done in biological warfare in both Britain and the United States at first. In the United Kingdom the preoccupation was mainly in withstanding the anticipated conventional bombing attacks that would be unleashed in the event of war with Germany. As tensions increased, Sir Frederick Banting began lobbying the British government to establish a research program into the research and development of biological weapons to effectively deter the Germans from launching a biological attack. Banting proposed a number of innovative schemes for the dissemination of pathogens, including aerial-spray attacks and germs distributed through the mail system.

With the onset of hostilities, the Ministry of Supply finally established a biological weapons programme at Porton Down, headed by the microbiologist Paul Fildes. The research was championed by Winston Churchill and soon tularemia, anthrax, brucellosis, and botulism toxins had been effectively weaponized. In particular, Gruinard Island in Scotland, during a series of extensive tests was contaminated with anthrax for the next 48 years. Although Britain never offensively used the biological weapons it developed, its program was the first to successfully weaponize a variety of deadly pathogens and bring them into industrial production.[31]

When the United States entered the war, mounting British pressure for the creation of a similar research program for an Allied pooling of resources, led to the creation of a large industrial complex at Fort Detrick, Maryland in 1942 under the direction of George W. Merck.[32] The biological and chemical weapons developed during that period were tested at the Dugway Proving Grounds in Utah. Soon there were facilities for the mass production of anthrax spores, brucellosis, and botulism toxins, although the war was over before these weapons could be of much operational use.[33]

However, the most notorious program of the period was run by the secret Imperial Japanese Army Unit 731 during the war, based at Pingfan in Manchuria and commanded by Lieutenant General Shir Ishii. This unit did research on BW, conducted often fatal human experiments on prisoners, and produced biological weapons for combat use.[34] Although the Japanese effort lacked the technological sophistication of the American or British programs, it far outstripped them in its widespread application and indiscriminate brutality. Biological weapons were used against both Chinese soldiers and civilians in several military campaigns
. Three veterans of Unit 731 testified in a 1989 interview to the Asahi Shimbun, that they contaminated the Horustein river with typhoid near the Soviet troops during the Battle of Khalkhin Gol.[35] In 1940, the Imperial Japanese Army Air Force bombed Ningbo with ceramic bombs full of fleas carrying the bubonic plague.[36] A film showing this operation was seen by the imperial princes Tsuneyoshi Takeda and Takahito Mikasa during a screening made by mastermind Shiro Ishii.[37] During the Khabarovsk War Crime Trials the accused, such as Major General Kiyashi Kawashima, testified that as early as 1941 some 40 members of Unit 731 air-dropped plague-contaminated fleas on Changde. These operations caused epidemic plague outbreaks.[38]

Many of these operations were ineffective due to inefficient delivery systems, using disease-bearing insects rather than dispersing the agent as a bioaerosol cloud.[34] Nevertheless, some modern Chinese historians estimate that 400,000 Chinese died as a direct result of Japanese field testing and operational use of biological weapons.[39]

Ban Shigeo, a technician at the Japanese Army's 9th Technical Research Institute, left an account of the activities at the Institute which was published in "The Truth About the Army Nororito Institute".[40] Ban included an account of his trip to Nanking in 1941 to participate in the testing of poisons on Chinese prisoners.[40] His testimony tied the Noborito Institute to the infamous Unit 731, which participated in biomedical research.[40]

During the final months of World War II, Japan planned to utilize plague as a biological weapon against U.S. civilians in San Diego, California, during Operation Cherry Blossoms at Night. They hope that it would kill tens of thousands of U.S. civilians and thereby dissuading America from attacking Japan. The plan was set to launch on September 22, 1945, at night, but it never came into fruition due to Japan's surrender on August 15, 1945.[41][42][43][44]

When the war ended, the US Army quietly enlisted certain members of Noborito in its efforts against the communist camp in the early years of the Cold War.[40] The head of Unit 731, Shiro Ishii, was granted immunity from war crimes prosecution in exchange for providing information to the United States on the Unit's activities.[45] Allegations were made that a "chemical section" of a US clandestine unit hidden within Yokosuka naval base was operational during the Korean War, and then worked on unspecified projects inside the United States from 1955 to 1959, before returning to Japan to enter the private sector.[40][46]

Some of the Unit 731 personnel were imprisoned by the Soviets[citation needed], and may have been a potential source of information on Japanese weaponization.

Considerable research into BW was undertaken throughout the Cold War era by the US, UK and USSR, and probably other major nations as well, although it is generally believed that such weapons were never used.

In Britain, the 1950s saw the weaponization of plague, brucellosis, tularemia and later equine encephalomyelitis and vaccinia viruses. Trial tests at sea were carried out including Operation Cauldron off Stornoway in 1952. The programme was cancelled in 1956, when the British government unilaterally renounced the use of biological and chemical weapons.

The United States initiated its weaponization efforts with disease vectors in 1953, focused on Plague-fleas, EEE-mosquitoes, and yellow fever - mosquitoes (OJ-AP).[citation needed] However, US medical scientists in occupied Japan undertook extensive research on insect vectors, with the assistance of former Unit 731 staff, as early as 1946.[45]

The United States Army Chemical Corps then initiated a crash program to weaponize anthrax (N) in the E61 1/2-lb hour-glass bomblet. Though the program was successful in meeting its development goals, the lack of validation on the infectivity of anthrax stalled standardization.[citation needed] The United States Air Force was also unsatisfied with the operational qualities of the M114/US bursting bomblet and labeled it an interim item until the Chemical Corps could deliver a superior weapon.[citation needed]

Around 1950 the Chemical Corps also initiated a program to weaponize tularemia (UL). Shortly after the E61/N failed to make standardization, tularemia was standardized in the 3.4" M143 bursting spherical bomblet. This was intended for delivery by the MGM-29 Sergeant missile warhead and could produce 50% infection over a 7-square-mile (18km2) area.[47] Although tularemia is treatable by antibiotics, treatment does not shorten the course of the disease. US conscientious objectors were used as consenting test subjects for tularemia in a program known as Operation Whitecoat.[48] There were also many unpublicized tests carried out in public places with bio-agent simulants during the Cold War.[49]

In addition to the use of bursting bomblets for creating biological aerosols, the Chemical Corps started investigating aerosol-generating bomblets in the 1950s. The E99 was the first workable design, but was too complex to be manufactured. By the late 1950s the 4.5" E120 spraying spherical bomblet was developed; a B-47 bomber with a SUU-24/A dispenser could infect 50% or more of the population of a 16-square-mile (41km2) area with tularemia with the E120.[50] The E120 was later superseded by dry-type agents.

Dry-type biologicals resemble talcum powder, and can be disseminated as aerosols using gas expulsion devices instead of a burster or complex sprayer.[citation needed] The Chemical Corps developed Flettner rotor bomblets and later triangular bomblets for wider coverage due to improved glide angles over Magnus-lift spherical bomblets.[51] Weapons of this type were in advanced development by the time the program ended.[51]

From January 1962, Rocky Mountain Arsenal grew, purified and biodemilitarized plant pathogen Wheat Stem Rust (Agent TX), Puccinia graminis, var. tritici, for the Air Force biological anti-crop program. TX-treated grain was grown at the Arsenal from 1962-1968 in Sections 23-26. Unprocessed TX was also transported from Beale AFB for purification, storage, and disposal.[52] Trichothecenes Mycotoxin is a toxin that can be extracted from Wheat Stem Rust and Rice Blast and can kill or incapacitate depending on the concentration used. The red mold disease of wheat and barley in Japan is prevalent in the region that faces the Pacific Ocean. Toxic trichothecenes, including nivalenol, deoxynivalenol, and monoace tylnivalenol (fusarenon- X) from Fusarium nivale, can be isolated from moldy grains. In the suburbs of Tokyo, an illness similar to red mold disease was described in an outbreak of a food borne disease, as a result of the consumption of Fusarium- infected rice. Ingestion of moldy grains that are contaminated with trichothecenes has been associated with mycotoxicosis.[53]

Although there is no evidence that biological weapons were used by the United States, China and North Korea accused the US of large-scale field testing of BW against them during the Korean War (19501953). At the time of the Korean War the United States had only weaponized one agent, brucellosis ("Agent US"), which is caused by Brucella suis. The original weaponized form used the M114 bursting bomblet in M33 cluster bombs. While the specific form of the biological bomb was classified until some years after the Korean War, in the various exhibits of biological weapons that Korea alleged were dropped on their country nothing resembled an M114 bomblet. There were ceramic containers that had some
similarity to Japanese weapons used against the Chinese in World War II, developed by Unit 731.[34][54]

Cuba also accused the United States of spreading human and animal disease on their island nation.[55][56]

During the 1948 Israel War of Independence, International Red Cross reports raised suspicion that the Israeli Haganah militia had released Salmonella typhi bacteria into the water supply for the city of Acre, causing an outbreak of typhoid among the inhabitants. Egyptian troops later claimed to have captured disguised Haganah soldiers near wells in Gaza, whom they executed for allegedly attempting another attack. Israel denies these allegations.[57][58]

In mid-1969, the UK and the Warsaw Pact, separately, introduced proposals to the UN to ban biological weapons, which would lead to the signing of the Biological and Toxin Weapons Convention in 1972. United States President Richard Nixon signed an executive order on November 1969, which stopped production of biological weapons in the United States and allowed only scientific research of lethal biological agents and defensive measures such as immunization and biosafety. The biological munition stockpiles were destroyed, and approximately 2,200 researchers became redundant.[59]

Special munitions for the United States Special Forces and the CIA and the Big Five Weapons for the military were destroyed in accordance with Nixon's executive order to end the offensive program. The CIA maintained its collection of biologicals well into 1975 when it became the subject of the senate Church Committee.

The Biological and Toxin Weapons Convention was signed by the US, UK, USSR and other nations, as a ban on "development, production and stockpiling of microbes or their poisonous products except in amounts necessary for protective and peaceful research" in 1972. The convention bound its signatories to a far more stringent set of regulations than had been envisioned by the 1925 Geneva Protocols. By 1996, 137 countries had signed the treaty; however it is believed that since the signing of the Convention the number of countries capable of producing such weapons has increased.

The Soviet Union continued research and production of offensive biological weapons in a program called Biopreparat, despite having signed the convention. The United States had no solid proof of this program until Dr. Vladimir Pasechnik defected in 1989, and Dr. Kanatjan Alibekov, the first deputy director of Biopreparat defected in 1992. Pathogens developed by the organization would be used in open-air trials. It is known that Vozrozhdeniye Island, located in the Aral Sea, was used as a testing site.[60] In 1971, such testing led to the accidental aerosol release of smallpox over the Aral Sea and a subsequent smallpox epidemic.[61]

During the closing stages of the Rhodesian Bush War, the Rhodesian government resorted to biological warfare. Watercourses at several sites close to the Mozambique border were deliberately contaminated with cholera and the toxin Sodium Coumadin, an anti-coagulant commonly used as the active ingredient in rat poison. Food stocks in the area were contaminated with anthrax spores. These biological attacks had little impact on the fighting capability of ZANLA, but caused considerable distress to the local population. Over 10,000 people contracted anthrax in the period 1978 to 1980, of whom 200 died. The facts about this episode became known during the hearings of the South African Truth and Reconciliation Commission during the late 1990s.[62]

After the 1991 Persian Gulf War, Iraq admitted to the United Nations inspection team to having produced 19,000 liters of concentrated botulinum toxin, of which approximately 10,000 L were loaded into military weapons; the 19,000 liters have never been fully accounted for. This is approximately three times the amount needed to kill the entire current human population by inhalation,[63] although in practice it would be impossible to distribute it so efficiently, and, unless it is protected from oxygen, it deteriorates in storage.[64]

According to the U.S. Congress Office of Technology Assessment 8 countries were generally reported as having undeclared offensive biological warfare programs in 1995: China, Iran, Iraq, Israel, Libya, North Korea, Syria and Taiwan. Five countries had admitted to having had offensive weapon or development programs in the past: United States, Russia, France, the United Kingdom, and Canada.[65] Offensive BW programs in Iraq were dismantled by Coalition Forces and the UN after the first Gulf War (199091), although an Iraqi military BW program was covertly maintained in defiance of international agreements until it was apparently abandoned during 1995 and 1996.[66]

On September 18, 2001 and for a few days thereafter, several letters were received by members of the U.S. Congress and American media outlets which contained intentionally prepared anthrax spores; the attack sickened at least 22 people of whom five died. The identity of the bioterrorist remained unknown until 2008, when an official suspect, who had committed suicide, was named. (See 2001 anthrax attacks.)

Suspicions of an ongoing Iraqi biological warfare program were not substantiated in the wake of the March 2003 invasion of that country. Later that year, however, Muammar Gaddafi was persuaded to terminate Libya's biological warfare program. In 2008, according to a U.S. Congressional Research Service report, China, Cuba, Egypt, Iran, Israel, North Korea, Russia, Syria and Taiwan are considered, with varying degrees of certainty, to have some BW capability.[67] By 2011, 165 countries had officially joined the BWC and pledged to disavow biological weapons.[68]

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