“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 Béchamp. 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 Béchamp 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 Béchamp 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.
This author realized years ago that inoculations caused the transformation of IgA into IgE; however, thanks to researcher Patrick Jordan finding the NATO Life Sciences book entitled “Immunological Adjuvants and Vaccines” (6), it has now been revealed that it is the aluminum which is put into vaccines as an adjuvant which causes production of IgE…the antibody of allergy and anaphylactic shock. This shocking admission comes in this book after the statement on page 6 that aluminum “was introduced in 1926, before strict control by regulatory authorities was practiced; whether it would be allowed by regulatory authorities today is far from certain”.
On page 37 of this NATO book, it states that studies demonstrate that “aluminum causes stimulation of the production of anaphylactic antibody (IgE) in the mouse”, and that “the effect of aluminum on the IgE response in humans does not appear to have been investigated”. This is just like the statement in the package insert of all vaccines (including the Gardasil vaccine which alleges it protects against cervical cancer) that “no studies have been done to evaluate for the potential to cause carcinogenicity or genotoxicity”. However, these experiments are being carried out in children every time they are inoculated with disease…and the skyrocketing allergies, anaphylactic reactions and cancer make it self evident that the inoculations are behind it all. Thanks to the book, I now have the evidence that IgE production is due to vaccines, as well as the fact that these mad scientists know exactly what they are doing. If this is not evidence of crimes against humanity, what is?
Additionally, 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 .
Although Dr. Browning’s research is intended to stimulate the pharma cartels to produce drugs to modulate B cell function in autoimmune disease; this document makes it SELF EVIDENT that the way to stop autoimmune disease from developing in the first place is to stop inoculating people and pets with disease, which is what causes the corruption of the immune system leading to autoimmune disease in the first place! Dr. Browning’s article discusses many of the following autoimmune diseases; in fact, he proves that even “neuropsychiatric disorders” can be produced by autoantibodies to N-methyl-D-aspartate (NMDA) receptors; thus explaining why even clients with “mental disease” respond to the Hippocrates protocol developed by Dr. Carley to detoxify vaccine viruses (and other toxins) using homeopathic nosodes!
Thus, the autoimmune disease you develop is determined by which tissues in the body are attacked by auto antibodies. If the inside lining of the gastrointestinal tract (the mucosa) is attacked by auto-antibodies you develop leaky gut syndrome (which leads to food allergies when partially digested food particles are released into the bloodstream, are recognized as antigens foreign to the body, and elicit an antibody response against those food particles that becomes heightened every time that same food is eaten and released into the bloodstream partially digested again). Crohn’s disease and colitis are also caused by auto-antibody attack on the mucosa of the GI tract itself. If the islet (insulin producing) cells of the pancreas are attacked by auto-antibodies, you develop insulin dependent (juvenile) diabetes. If the respiratory mucosa is attacked by auto-antibodies, you develop “leaky lung” syndrome where, just as with leaky gut, antigens recognized as foreign to the body which are inhaled are able to traverse the lining of the respiratory tract, causing the creation of antibodies against those antigens (usually dust, mold, pet or pollen antigens). When these substances are inhaled again, IgE (the pathologic form of IgA created after corruption of the immune system due to inoculation rather than inhalation of disease) acts as a reagin4 and sensitizes mast and basophil cells, causing release of their histamine and slow reacting substance granules on contact with the allergen to produce constriction of the bronchioles leading to asthma. This process is also responsible for the immediate hypersensitivity reaction known as anaphylaxis, which is a potential side effect noted in the Physician’s Desk Reference for every vaccine; as well as the wheal and flare reaction of the skin known as hives. If the components of the articular surface of the joints are attacked by auto-antibodies, you develop rheumatoid (or juvenile) arthritis. If the skin is compromised on a chronic basis, you develop “leaky skin” syndrome, where contact antigens which could not otherwise traverse the skin lead to skin allergies to contact antigens (a delayed hypersensitivity reaction where inflammation occurs due to release of soluble factors). Additionally, depending on which level of the skin is attacked by auto-antibodies, (i.e., the epidermis or dermis), you develop eczema, psoriasis or scleroderma. If the kidney tissue is attacked by auto-antibodies, you develop one of the many types of nephritis, depending on which component of renal tissue is attacked (for example, with glomerulonephritis, the basement membrane of the glomerular apparatus within the kidney (which filters blood to form urine) is attacked by auto-antibodies, thus allowing protein to escape from the serum into the urine). If you develop auto-antibodies against thyroid gland tissue, you develop Grave’s disease. If you develop auto-antibodies against the tissue of the thymus gland (which is crucial in T cell production and function), you develop myasthenia gravis. If you develop auto-antibodies against the very DNA in the nucleus of all cells, you develop systemic Lupus (thus, the autoimmune potential of DNA vaccines being developed now is self evident; worse yet, DNA components from these vaccines can be incorporated into your DNA, leading to actual genetic changes which could cause extinction of all (vaccinated) life on the Earth, as will be discussed shortly). And on, and on, and on.
The brain and spinal cord can also be attacked with auto-antibodies (which this author refers to as vaccine induced encephalitis), leading to a variety of neurological diseases. The most severe of these, leading to death, are sudden infant death syndrome (SIDS) and most cases of “shaken baby syndrome”. If components of the myelin sheath (the insulating covering of nerve fibers which allows proper nerve conduction) or the actual neurofilaments themselves are attacked by auto-antibodies, the resultant condition is determined solely by the location of the damage done. Such neurological conditions include but are not limited to minimal brain dysfunction, ADD/ADHD, learning disabilities, mental retardation, criminal behavior, the spectrum of pervasive developmental disorders (including autism), multiple sclerosis, Parkinson’s disease, Lou Gehrig’s disease, Guillen Barre’, seizure disorders, etc., etc. etc. (Please note that other factors are also sometimes involved, such as: the spirochete which causes Lymes disease, aspartame and mercury in cases of MS; aspartame in seizures; or pesticides in cases of Parkinson’s). Thus, when detoxing to reverse these diseases, these other substances must also be removed to obtain a full recovery. However, the corruption of the immune system caused by the injection of vaccines is a key component in these disease states leading to immune malfunction, and is the reason why an autistic child may also have leaky gut or eczema, etc. Note that myelin production, for the most part, does not begin until after birth. Most myelin is apparently laid down by age 5 years and usually completed by age 10 years, judging by the level of success at various ages in reversing autistic and other neurological VIDS symptoms that this author has observed in hundreds of children by detoxing the viruses with homeopathic nosodes5, and repairing the immune corruption by simultaneous administration of bovine colostrum (i.e., after 10 years of age, the ability to stop and repair auto-antibody induced damage in the myelin sheath and neurofilaments themselves is dramatically decreased).
In summary, the hyperactivity of the humoral arm of the immune system in autoimmune disease is caused by adjuvants added just for that purpose. However, the damage caused by the autoimmunity itself (i.e., antibody against self) has several mechanisms, including the following:
- The antigens present in the culture media itself cannot be completely filtered and separated from the organisms cultured thereon. Thus, any antibodies formed against antigens from the culture cells themselves (for example myelin basic protein from chick embryos or the 13 vaccines which now contain aborted human fetal cells) can cross-react to form an autoimmune reaction against the myelin basic protein in your myelin sheath, etc. See the package insert from Pfizer’s Rabies vaccine from the “10th Edition of the Compendium of Veterinary Products” published in 2007 posted on www.drcarley.com, which states “tissue origin vaccines contain extraneous protein in addition to the [rabies] antigen that can lead to autoimmune disease”. THIS IS TRUE FOR ALL VACCINES, BUT THIS IS THE FIRST TIME I HAVE SEEN IT ADMITTED BY ANY VACCINE MANUFACTURER.
- Molecular mimicry is due to similarity of proteins contained in organisms and mammals. (For example, the measles virus is made up of proteins similar to myelin basic protein; thus, antibodies formed against the measles virus antigens subsequently also cause an auto-antibody attack against myelin basic protein in the myelin sheath due to cross reactivity of these antibodies).
- Formation of immune complexes occur as antigens and antibodies interlock into clusters which can then become trapped in various tissues, especially the kidneys, lung, skin, joints, or blood vessels. Once trapped, these complexes then set off an inflammatory reaction which lead to further tissue damage.
- Intentional inclusion of antigens in vaccines to cause formation of antibodies that attack specific hormones or races. It is this author’s hypothesis that the epidemic of vitiligo in people of color (hypo pigmentation of skin caused by auto-antibody attack on melanocytes7) is occurring due to intentional inclusion of melanin in vaccines given to people of color. Additionally, experiments done on women of childbearing age in the Philippines and probably other locations where HCG (human chorionic gonadotropin) placed into vaccines given these women resulted in antibodies against the HCG hormone, and subsequent spontaneous abortion thus occurred when the women became pregnant. The NATO book “Immunological Adjuvants and Vaccines” also describes, in the chapter entitled “The Development and Preliminary Clinical Evaluation of an Antifertility vaccine” (6) how an antifertility vaccine has been developed incorporating HCG in a vaccine with diphtheria toxoid; and that the vaccine will soon be suitable for “large scale clinical use”. The “task force” (which involves many agencies within the World Health Organization in this chapter’s references) “is in the process of developing other fertility regulating vaccines as well”. Could the escalating problems with infertility in this country be due to women having been given this vaccine without their knowledge or consent?
Another heinous (and obviously genocidal) creation of the Anti-Hippocratics is the DNA vaccines now being developed. These vaccines contain plasmids, which are closed rings of recombinant DNA that make their way into the nucleus of a cell and instruct the cell to synthesize encoded antigenic proteins8. Thus, the very genetic makeup of the individual, plant or animal will be altered to produce a never ending supply of antigens to distract the immune system. These genetic changes will remain as cell division occurs, and will be transmissible to offspring. This is the TRUE “mark of the beast” , and could lead to extinction and/or modification (including behavioral) of any group inoculated.
In addition to the above phenomena which lead to simultaneous depression of cellular immune function and hyperactivity of humoral immune function, vaccines also contain other toxic substances which can cause serious side effects themselves. The following ingredients are actually listed on the CDC website with this introductory statement: “Many things in today’s world, including food and medicines, have chemicals added to them to prevent the growth of germs and reduce spoilage.” Translation: you’re already toxic, so what’s the big deal with adding more poison? This author’s answer to that question is that any immunotoxin can end up being the “straw that breaks the immune system’s back” in that individual, leading to dis-ease. This is where genetics is key; i.e., not that what disease you develop is actually caused by some “gene” in most cases; but rather that your genes determine the strength of your immune system (i.e., how many assaults your immune system can take before it reaches critical mass, and you develop a dis-ease).
Some additional ingredients in vaccines (as listed by the CDC on their website) include antibiotics, aluminum gels, formaldehyde, monosodium glutamate (MSG), egg protein, and sulfites. Thus, we have antibiotics (which you could be allergic to); aluminum (which when combined with dead neurons killed by mercury in vaccines as demonstrated in the video at http://www.youtube.com/watch?v=85tgwh3HpsM) results in the neurofibrillary tangles seen in Alzheimer’s disease); formaldehyde (a toxic carcinogenic substance used to preserve dead people); MSG ( a potent excitotoxin9 which, like aspartame, can cause seizures, brain tumors, etc.); egg protein (to which you could have a life threatening anaphylactic reaction); and sulfites (another toxin which we are advised not to consume much of orally, but in vaccines, it is injected directly into the body). Is this not a veritable witch’s brew of chemicals, organisms, and animal parts? What the CDC does NOT list is that 13 vaccines at present (and more are in the works) are actually cultured on aborted human fetal tissues (go to www.cogforlife.org for more info). THIS IS CANNIBALISM. Note in this list that they also fail to mention the ethyl-mercury containing preservative thimerosol, which has been the only dangerous substance in vaccines to receive mainstream media attention (albeit most of that being disinformation) after the explosion in the rate of occurrence of autism in the last generation became self-evident proof that vaccines are the causative factor. For, although the scientists working for the medical mafia continue to use statistics to twist and spin their data to make us beLIEve that vaccines are not the cause, too many thousands of parents have watched their children enter the downward spiral into autism after their children received the vaccine which was the straw that broke the back of their child’s immune system. No matter what the “white coats” tell these parents, they know the truth!
Mercury (also in dental amalgam fillings) is a highly toxic heavy metal, has been documented to cause cancer, and can be absorbed through the digestive track, skin, and respiratory track. Mercury is 1,000 times more toxic than lead, and is second only to uranium as the most toxic metal. If children receive all recommended vaccines, they will receive many times the “allowable safe limit” for mercury in the first two years of life (as if there is such a thing as a “safe” amount of a toxic poison). Yet, even after Congressional hearings instigated by Congressman Dan Burton (whose own grandchild became autistic after receiving vaccines) resulted in the FDA requesting (not ordering) vaccine manufacturers to remove this toxic heavy metal from their products, mercury is still present in many vaccines.
Although the symptoms of mercury poisoning have been described as identical to the symptoms of autism, it should be noted that most children who descend into the hellish state known as autism do so after the MMR vaccine. The MMR vaccine is one of the few vaccines that do not contain mercury; in fact, it has NEVER contained mercury. Thus, it is self-evident that the removal of mercury will not make vaccines “safe”. (This is why the mercury is the only thing being addressed at all; because when the people reading this paper realize that the very mechanism by which vaccines corrupt the immune system means that NO vaccine is safe and effective; there will be an evolution of consciousness where the structure of lies telling us vaccines are safe and effective disintegrates.)
The good news is that these VIDS can be reversed using natural remedies (especially homeopathy) contained in the Hippocrates Protocol (www.drcarley.com). This “surgical strike” detoxification approach which has the potential to reverse ALL of the aforementioned conditions under the VIDS umbrella as long as detoxification is started early enough will be the one truth put on top of the mountain of lies (that vaccines are safe and effective) that will cause the entire mountain of vaccine lies to crumble. Thus, the vaccine-induced holocaust (where instead of people being put in concentration camps, the concentration camps are being put into the people) will finally be put to an end. In this author’s opinion, it will be the reversal of VIDS (especially autism) in children and reversal of Gulf War Syndrome in the vaccine damaged soldiers and vets which will stop this holocaust on humanity caused by vaccines, since the reversal of dis-ease subsequent to detoxification of the vaccines makes it self-evident that the vaccines caused the problem.
Unfortunately, we can no longer pretend that this epidemic of VIDS is merely a “mistake” made by well intentioned, albeit misguided mad scientists. Because it’s even worse than the above, folks…we are talking TREASON and CRIMES AGAINST HUMANITY, PETS, and even PLANTS, (which are also being genetically modified to create vaccines). The evidence for this is as follows:
As concern for population growth started to grow and the final plans to bring in the New World Order were put in place, this lie called vaccines was transformed into pure evil, as it was realized that such delivery systems could be used to intentionally cause disease, which is now being done under the US Code, Title 50, Chapter 32, § 1520 and 1524. You can read it for yourself at your local library. [Barb’s note: here is a link – http://www.law.cornell.edu/uscode/50/usc_sup_01_50_10_32.html]
This law has been in place since the 1960’s, and it was last modified in April of 2000. The only stipulation made for experimentation on human subjects is that local civilian officials be notified 30 days before the experiment is started. Section 1524 adds that the Secretary of Defense may enter into agreements with the Secretary of Health and Human Services to provide support for vaccination programs through use of excess peacetime biological weapons (i.e., weapons of mass destruction). In April 2000, § 1520 (a) was passed to put alleged restrictions on the use of human subjects for testing of chemical or biological agents after a caller on C Span mentioned this law in 1999, which revealed this treasonous law to a huge audience of listeners (including this author, who has been including it in lectures and written materials since that call came into “Washington Journal”). However, the exceptions written to Title 50, chapter 32 under § 1520 subsection (b) in the 2000 law passed by our aiders and abettors of treason in Congress not only loophole back in a test carried out for “any peaceful purpose that is related to a medical, therapeutic, pharmaceutical, agricultural, industrial, or research activity”; but add that such biological and chemical warfare agents can now be also used for any law enforcement purpose, including “any purpose related to riot control” (just in case those C Span listeners should actually get off the couch at the horror of what the traitors in Washington, D.C. are doing to God’s people). Subsection (c) of this law now mandates that “informed consent” be required. In reality, not a single vaccine has ever been tested for its long term side effects (including carcinogenic potential). Additionally, the intentional introduction into vaccines of stealth viruses, (including man-made viruses that cause cancer, mycoplasma and the HIV virus), antigens which target certain races, and silicon and/or DNA chips in the future makes it self evident that informed consent is impossible, as it would initiate impeachment proceedings and war crimes trials against every “public servant” involved in perpetrating these crimes against the American people, in violation of the Nuremberg Code (which was written after the end of WW II to prevent the barbaric experiments that occurred in the Nazi concentration camps) . What most people don’t know is that the top level mad scientists from Nazi Germany were actually brought to the United States after the war through “Operation Paperclip”, and have been continuing their work to this day in places like Brookhaven labs, Cold Spring Harbor and Plum Island in this author’s backyard on Long Island. In 1969 the U.S. military/CIA and Rockefeller directed National Academy of Sciences-National Research Council (NAS-NRC) announced that a research program to explore the feasibility of “creating a new infective microorganism. [HIV].which would be refractory to the immunological and therapeutic processes upon which we depend to maintain our relative freedom from infectious disease” could be completed at a total cost of $10 million. Yes, this is what your tax dollars are going towards, folks. But hang on to your hat, because it only gets worse.
Dr. James R. Shannon, former director of the National Institute of Health reported in December, 2003 that “the only safe vaccine is one that is never used”. However, the reverberating truth, “the shot heard round the world” which will lead to the evolution of consciousness necessary to stop the holocaust against humanity known as vaccinations, will be that not only are vaccinations not safe or effective, but that they are actually weapons of mass destruction being perpetrated upon humanity in the name of health, for the purpose of genocide and to bring in the New World Order. Part 2 of the genocidal plan could drop anytime with activation of the Model State Health Emergency Powers Act whenever the next fabricated terrorist attack using biological agents occurs. The “bird flu” is apparently going to be used as an excuse to inoculate the masses soon, as predictions of a pandemic are being made by the media almost every day. Little do people know that the 1918 Flu pandemic was actually caused by inoculations given to soldiers in WW 1, as reported on p. 28 of the book Vaccination the Silent Killer by Ida Honorof & E. McBean.
The Congressional traitors in Washington posing as public “servants” are doing all they can to pass “Codex” legislation which will make the natural remedies and supplements used in the Hippocrates Protocol developed by this author to reverse all dis-eases only available by prescription. So, you didn’t hear about that on your local news station either? Please go to the site of John Hamill of the International Alliance for Health Freedom (who reversed his schizophrenia symptoms with these natural supplements and has dedicated his life to stopping Codex from passing) at www.iahf.com .
Wake up, America-it’s getting very late….it is time for the mountain of lies to crumble. Please spread the world to everyone you know….we will make it happen! The time to stop chopping at branches and get to the root of this evil is now! Traitors to America include William Atkinson, MD, MPH of the National Immunization Program at the CDC. On December 9, 2004, Dr. Atkinson informed a NYS Department of Health minion that a child to whom this author had given a medical exemption from further inoculation “should be vaccinated unless he has an anaphylactic allergy to hepatitis B vaccine” as there is “no such syndrome [as VIDS]”. Yet, in a document published by the CDC on May 4, 2000 (# 99-6194) entitled “Vaccine Information Statements; What You Need to Know”, on page 9 the following is printed under the heading “The Law (Recording Patient Information and Reporting Adverse Events): 42 U.S.C. § 300aa-25. Recording and Reporting of Information, (b) Reporting (2) “A report under paragraph (1) respecting a vaccine shall include the time periods after the administration of such vaccine within which vaccine-related illnesses, disabilities, injuries, or conditions the symptoms and manifestations of such illnesses, disabilities, injuries, or conditions, or DEATHS occur, and the manufacturer and lot number of the vaccine.” Thus, while Dr. Atkinson informed this author on January 8, 2005 that “having a judge in the Bronx Family Court “qualify” you as an “expert witness” neither makes you an expert, nor proves the existence of so called “vaccine induced disease syndrome”; the CDC’s own documents refer to the federal mandate for such to be reported to the secretary. Dr. Atkinson, who received a copy of the draft of this paper on 12/30/04, has not offered a single rebuttal to the mechanism whereby the mechanism of VIDS is explained in this paper. Ergo, this author hereby formally charges Dr. Atkinson and his co-conspirators in the CDC with the following counts, including but not limited to:
01.) False statements within a Government Agency, Title 18 USC § 35.1001.
02.) WAR CRIMES – crimes when death occurs, Title 18 USC § 34.
03.) Concealment, removal – Title 18 USC § 2071.
04.) Aiding and Abetting, Title 18 USC § 3.
05.) Obstruction of Justice, Title 18 USC § 1505 / USC § 2 (26).
06.) Defrauding America, Title 18, USC § 1101 (25).
If the People lead, the “leaders” will follow. SILENCE IS CONSENT. If you do nothing, before long highly trained Special Operations commandos with state of the art weaponry will be used in the U.S. to “execute quarantine and certain health laws”, including the Model State Health Emergency Powers Act passed in all states where, following another domestically perpetrated biological scare (such as the anthrax mailings to the Congress), a solution in the form of a vaccine will be offered only to those who will accept the national ID chip being injected into them. All others will be considered a danger and threat to society, hunted down, and imprisoned in concentration camps already built or be killed. Americans will welcome this solution, and turn in their neighbors or friends in order to survive themselves. If you are not part of the solution, therefore, you are part of the problem. Please do all you can to make this happen. It is now in your hands, People of the United States of America.
In conclusion, the 1920 book “Horrors of Vaccination Exposed and Illustrated; Petition to the President to Abolish Compulsory Vaccination in the Army and Navy” by Charles M. Higgins, was recently found by this author, and gives the best explanation as to why the compulsory blood assault known as “vaccination” is unconstitutional and unlawful. This book is now in the public domain and can be viewed and downloaded by clicking on the pdf file on www.drcarley.com. Better yet, Dr. True Ott (a regular guest on “What’s Ailing America?”) has had this book re-published. I ask each of you to call his office at 866-989-9876 and order several copies. Send this book to your legislators in every state, and demand they explain on what legal basis they are compelling children to undergo a blood assault to attend school, based on the constitutional arguments written by Mr. Higgins. I am presently searching for an attorney of conscience to bring a lawsuit at the federal level to stop this insanity…before the Model State Health Emergency Powers Act is used on a mass scale to inoculate the public with the bird flu vaccine, which will cause the bird flu pandemic.
Respectfully submitted by Rebecca Carley, MD
 “IMMUNOLOGY” by Ronald D. Guttman, MD, Professor of Medicine, McGill University, et. al., (ISBN # 0-89501-009-7), 1983.
 Pathologic = pertaining to or caused by disease
 Auto antibodies = antibodies produced by the body that attacks its own tissues.
 Reagin = antibody of a specialized immunoglobulin class (IgE) which attaches to tissue cells of the same species from which it is derived, and which interacts with its antigen to induce the release of histamine and other vasoactive amines.
 A nosode is a homeopathically prepared remedy, made from a disease or a pathological product. Nosodes are used in the same way as vaccines; they sensitize the body, prompting the immune system to react (and detox, or eliminate, the offending agent). However, as they are extremely dilute and oral in application, they do not lead to the corruption of the immune system caused by inoculation with disease.
 “:IMMUNOLOGICAL ADJUVANTS AND VACCINES” edited by Gregory Gregoriadis, Anthony C. Allison and George Poste, NATO ASI Series, Series A: Life Sciences Vol. 179, (ISBN 0-306-43386-9), 1989, Plenum Press, New York.
(Human chorionic gonadotropin = the hormone produced when women first become pregnant)
 Melanocytes = melanin producing cells in skin
 “GENETIC VACCINES”, Scientific American, July 1999, pgs 50-57 @ p. 52, which can be reviewed at http://sciamdigital.com/index.cfm?fa=Search.ViewSearchForItemResultList (if you pay the $7.95 fee). Put “Genetic Vaccines” in the search engine.
 Excitotoxins are usually amino acids, such as glutamate and aspartate. These special amino acids cause particular brain cells to become excessively excited, to the point they will quickly die. Excitotoxins can also cause a loss of brain synapses and connecting fibers. Food-borne excitoxins include such additives as MSG and aspartame, both toxic substances approved for use in humans by the FDA (Fraudulent Drug Administration).
 “color of law” = the appearance or semblance, without the substance, of legal right. Misuse of power, possessed by virtue of state law and made possible only because wrongdoer is clothed with authority of state, is action taken under “color of state law”. Atkins v. Lanning, D.C.Okl., 415 F.Supp. 186, 188.
Action taken by private individuals may be “under color of state law” for purposes of 42 U.S.C.A. § 1983 governing deprivation of civil rights when significant state involvement attaches to action. Wagner v. Metropolitan Nashville Airport Authority, C.A.Tenn., 772 F.2d 227, 229.
Acts “under color of any law” of a State include not only acts done by State officials within the bounds or limits of their lawful authority, but also acts done without and beyond the bounds of their lawful authority; provided that, in order for unlawful acts of an official to be done “under color of any law”, the unlawful acts must be done while such official is purporting or pretending to act in the performance of his official duties; that is to say, the unlawful acts must consist in an abuse or misuse of power which is possessed by the official only because he is an official; and the unlawful acts must be of such a nature or character, and be committed under such circumstances, that they would not have occurred but for the fact that the person committing them was an official then and there exercising his official powers outside the bounds of lawful authority. 42 U.S.C.A. § 1983.
(The above definitions are from Black’s law dictionary, 6th edition, pgs. 265-266)
The author wishes to thank Mr. Chris Barr for his invaluable additions and editorial assistance in the writing of this document; and Meryl Dorey of the Australian Vaccination Network, Inc., whose additions for the publication of this paper in their magazine “Informed Choice” in Australia have also been invaluable.