This is long, but well worth the read. The only thing that i disagree with here 
concerning vaccines is that Monsanto has the #1 weapon of mass destruction and 
that vaccines are actually #2. This article is VERY informative and will help 
many to connect crucial dots in this nightmare many of us have now come to know 
as reality. Vaccines were created for nothing more than to cause sickness and 
death. The more people come to terms with this truth, the more lives will be 
saved. The funny thing about this is that i have to go back and read this from 
time to time and the more i learn the more this article makes sense to me. The 
more dots i'm able to connect. Please read for yourselves and see what you 
think. I would love to hear your thoughts. 

Please send this to all you know, but please remove my email address. 

Connie 



INOCULATIONS: THE TRUE WEAPONS OF MASS DESTRUCTION 
CAUSING VIDS (VACCINE INDUCED DISEASES) 
(AN EPIDEMIC OF GENOCIDE) 
by Rebecca Carley, M.D. 
Court Qualified Expert in VIDS and Legal Abuse Syndrome 

Amended January 21, 2007 

PDF - download < right click and "save-as" to your hard drive 


"One basic truth can be used as a foundation for a mountain of lies, and if 
we dig down deep enough in the mountain of lies, and bring out that truth, to 
set it on top of the mountain of lies; the entire mountain of lies will crumble 
under the weight of that one truth. And there is nothing more devastating to a 
structure of lies than the revelation of the truth upon which the structure of 
lies was built, because the shock waves of the revelation of the truth 
reverberate, and continue to reverberate throughout the Earth for generations 
to 
follow, awakening even those people who had no desire to be awakened to the 
truth." (by Delamar Duvaris as written in the preface of "Behold the Pale 
Horse" by William Cooper). 
The basic truth that served as the foundation for the mountain of lies 
known as vaccinations was the observation that mammals which recover from 
infection with microorganisms acquire natural immunity from further infections. 
Whenever cytotoxic T cells (the little Pac man cells which devour and 
neutralize 
viruses, bacteria, and cancer cells, thus conferring cellular immunity and are 
also responsible for allograft rejection) and B cells (antibody producing cells 
which confer humoral immunity by circulating in the body's fluids or "humors", 
primarily serum or lymph) are activated by various substances foreign to the 
body called antigens, some of the T and B cells become memory cells. Thus, the 
next time the individual meets up with that same antigen, the immune system can 
be quickly triggered to demolish it. This is the process known as natural 
immunity. 
This truth gave birth to a beLIEf that if a foreign antigen was injected 
into an individual, that individual would then become immune to a future 
infection. This beLIEf, (you see the lie in the middle), was given the name, 
"vaccinations". What the promoters of vaccination failed to realize is that 
secretory IgA (an antibody found predominately in saliva and secretions of the 
gastrointestinal and respiratory tract mucosa) is the initial normal antibody 
response to all airborne and ingested pathogens. IgA helps protect against 
viral 
infection, agglutinate bacteria, neutralize microbial toxins, and decrease 
attachment of pathogens to mucosal surfaces. What this author has realized is 
that bypassing this mucosal aspect of the immune system by directly injecting 
organisms into the body leads to a corruption in the immune system itself 
whereby IgA is transmuted into IgE, and/or the B cells are hyperactivated to 
produce pathologic amounts of 
self-attacking antibody as well as suppression of cytotoxic T cells (as 
explained shortly). As a result, the pathogenic viruses or bacteria cannot be 
eliminated by the immune system and remain in the body, where they cause 
chronic 
disease and thus further grow and/or mutate as the individual is exposed to 
ever 
more antigens and toxins in the environment. This is especially true with 
pathogens grouped under the term "stealth adapted". These are formed when 
vaccine viruses combine with viruses from tissues used to culture them, or when 
bacteria lose their cell walls when a person takes antibiotics and transform 
into "L forms", leading to a lack of some critical antigens normally recognized 
by the cellular immune system. Another example is stealth adapted (mutated) 
cytomegaloviruses which arose from African green monkey (simian) kidney cells 
when they were used to culture polio virus for live polio virus vaccines. Thus, 
not only was the vaccinee 
inoculated with polio, but with the cytomegalovirus as well. 
The mechanism by which the immune system is corrupted can best be realized 
when you understand that the two poles of the immune system (the cellular and 
humoral mechanisms) have a reciprocal relationship in that when the activity of 
one pole is increased, the other must decrease. Thus, when one is stimulated, 
the other is inhibited. Since vaccines activate the B cells to secrete 
antibody, the cytotoxic (killer) T cells are subsequently suppressed. (In fact, 
progressive vaccinia (following vaccination with smallpox) occurs in the 
presence of high titers of circulating antibody to the virus1 combined with 
suppressed cytotoxic T cells, leading to spreading of lesions all over the 
body). This suppression of the cell mediated response is thus a key factor in 
the development of cancer and life threatening infections. In fact, the 
"prevention" of a disease via vaccination is, in reality, an inability to expel 
organisms due to the suppression of the 
cell-mediated response. Thus, rather than preventing disease, the disease is 
actually prevented from ever being resolved. The organisms continue circulating 
through the body, adapting to the hostile environment by transforming into 
other 
organisms depending on acidity, toxicity and other changes to the internal 
terrain of the body as demonstrated by the works of Professor Antoine B�champ. 
He established this prior to the development of the "germ theory" of disease by 
Louis Pasteur. Pasteur's "germ theory" was a plagiarist's attempt to reshape 
the truth from B�champ into his own "original" premise � the beLIEf that germs 
are out to "attack" us, thereby causing dis-ease. Thus, treatment of infection 
with antibiotics as well as "prevention" of disease with vaccines are both just 
corrupted attempts at cutting off the branches of dis-ease, when the root of 
the 
cause is a toxic internal environment combined with nutritional deficiency. 
However, since 
Pasteur's germ theory was conducive to the profits of the burgeoning 
pharmaceutical cartels that only manage dis-ease, no mention of the work of 
Professor B�champ is made in medical school curricula. 
To make matters worse than the suppression of cellular immunity which 
occurs when vaccines are injected, adjuvants (which are substances added to 
vaccines to enhance the antibody response) can actually lead to serious side 
effects themselves. Adjuvants include oil emulsions, mineral compounds (which 
may contain the toxic metal aluminum), bacterial products, liposomes (which 
allow delayed release of substances), and squalene. The side effects of 
adjuvants themselves include hyperactivity of B cells leading to pathologic2 
levels of antibody production, as well as allergic reaction to the adjuvants 
themselves (as demonstrated in Gulf War I soldiers injected with vaccines 
containing the adjuvant squalene, to which antibodies were found in many 
soldiers). Note that the pathologically elevated hyperactivity of antibody 
production caused by adjuvants also results in a distraction from the other 
antigens that the immune system encounters "naturally", 
which must be addressed to maintain health. 
In addition to the transmutation of IgA into IgE leading to allergic 
reactions described shortly, the overall hyperactivity of the humoral (antibody 
producing) pole of the immune system is, in this author's opinion, the sole 
cause of all autoimmune diseases; where the auto-antibodies produced activate 
functioning T cells to then attack self; and both the activated B & T cells 
also 
produce cytokines (which further enhance inflammation and immunological 
involvement). The only thing which determines which autoimmune disease you 
develop is which tissues in your body are attacked by auto-antibodies3. PLEASE 
NOTE THAT THIS FINDING HAS NOW BEEN CONFIRMED BY DR. JEFFREY BROWNING SENIOR 
DIRECTOR, DEPARTMENT OF IMMUNOBIOLOGY, BIOGEN-IDEC, IN HIS SCIENTIFIC PAPER 
ENTITLED "B CELLS MOVE TO CENTRE STAGE: NOVEL OPPORTUNITIES FOR AUTOIMMUNE 
DISEASE TREATMENT" PUBLISHED IN NATURE REVIEWS DRUG DISCOVERY 5, 564-576 (JULY 
2006); AVAILABLE ON THE INTERNET AT: 
http://www.nature.com/nrd/journal/v5/n7/full/nrd2085.html#a1 . 


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