Chemtrail Lab Analysis -
Virulent Bio-Toxin Soup
From Paul LeBreton <>
From John DeShiro
Regarding the post on Chemtrail Lab Analysis - Virulent Bio-Toxin Soup:
US Code Title 15 Section 1520 was repealed in 1997...
and replaced with1520a
...which contains much of the same wording with a different spin.
If you first take a tour to, click on the site map, then go to page 3 you will find where it states that they have to reduce the size of the human population by 'humane' means. This got me to wondering if they thought that chemical spraying was in their opinion a 'humane' means to reduce the population. I don't know if you have heard of William Thomas, but he has a lot of info on the chemtrails. His website is If you click on issue # 6 you can get a lot of information. He has posted on his site BIOWARFARE TEST ON THE AMERICAN PEOPLE.
This states that the recently revised U.S. Code Title 50, Section 1520 states that the Secretary of Defense may conduct tests or experiments "involving the use of a chemical agent or biological agent on a civilian population" if they are related to research activity. The law also stipulates that biowarfare test can be carried out on Americans only if Congress is notified 30 days in advance, and "only if informed consent to the testing was obtained from each human subject in advance of the testing on that subject."
There is plenty of pattern and precedent to suggest that clandestine biowarfare experiments are routinely pacticed on the American public without their informed consent. Two Congressional investigations in1977 and 1994 - and recently declassified British defense documents - detail 50 years of "open air" testing that used ships and spray-equipped aircraft to spread biological warfare simulaants on hundreds of cities across the U.S., Canada and the U.K. There is more to this article. I just wanted to give you some of the info because could spend the rest of the day typing this stuff up.
So far some of the chemicals that were collected from the chemtrail spray and lab tested is:
1. Bacilli & Molds 2. Pseudomonas Aeruginosa 3. Pseudomonas Florescens 4. Bacilli Amyloliquefaciens 5. Streptomyces 6. Enterobacteriaceae 7. Serratia Marcscens 8. Human White Blood Cells 9. A restricter enzyme used in research labs to snip and combine DNA 10. Enterobacter Cloacae 11. Other bacilli and other toxic molds capable of producing heart disease and meningitis, as well as acute upper respiratory and gastrointestinal distress. 12. JP-8 Jet Fuel = Ethylene Dibromide
# 2. Pseudomonas Aeruginosa = Respiratory tract infection by the ubiquitous bacterium. Cancer and burn patients also commonly suffer attack from this organism. Unlike other bacteria that reside in the enviroment, P. aeruginosa has a remarkable capacity to cause disease. Pseudomonas has the ability to adapt and thrive in many ecological niches, including humans. Once infections are established, P. aeruginosa produces a number of toxic proteins which cause not only extensive tissue damage, but also interfere with the human immunesystem's defense mechanisms. These proteins range from potent toxins that enter and kill host cells at or near the size of colonization todegradative enzymes that permantly disrupt the cell membranes and connective tissues in various organs. P. aeruginosa successfully colonizes the respiratory tract. One reason is that it produces a highly protective capsule made of the mucoid polysaccharide alginate. This allows the bacteria to resist engulfment by immune systemcells and better adhere to the lining of the lungs. It is likely that antibiotics cannot effectively eradicate Pseudomonas from the lungs because of this protective capsule. In addition, some Pseudomonas strains can inactivate the drugs that threaten them by using enzymes to modify the drug.
# 7. Serratia Marcescens is a significant opportunistic human bacterial pathogen. This microorganism has been shown to be the cause of many life-threatening diseases such as pneumonia, meningitis and endocarditis. It is one of the major causes of hospital-acquired infections. The seriousness of a S. marcescens infection is compounded by the fact that it is very resistant to most commonly used antibotics, thus making treatment difficult. In this study one of the factors contributing to the antibiotic resistance of S. marcescens will be examined. In order for an antibiotic to kill or inhibit growth of bacteria it must penetrate the outer surface or membrane and enter the bacterial cell which is very difficult. I hope some of this helps you to better understand what we are fighting against.
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