Posted: 19 January 2006
RESPONSE OF REBECCA CARLEY, MD (COURT QUALIFIED EXPERT IN VACCINE INDUCED DISEASES) TO CDC'S PUBLIC HEALTH PROTECTION RESEARCH GUIDE 2006-2015
( posted at http://www.rsvpbook.com/custom_pages/50942/chapter.php?cat_id=1 ) dated and submitted January 15, 2006
( can be accessed on CDC site at http://www.rsvpbook.com/custom_pages/50942/popup_chapter.php )
The CDC claims that its Research Guide "will provide a comprehensive, long-range vision of national and global public health needs that CDC and its partners can address through research. The Research Guide will help identify critical knowledge needed to achieve CDC's new health protection goals which are designed to maximize the health impact of programs, services, and emergency responses". In the media advisory asking for public comment it is claimed that "the wide-ranging Research Guide addresses topics of critical interest to the American public including finding new ways to combat infectious diseases such as pandemic influenza, and chronic diseases such as cancer and diabetes. It will be self evident from the documentation herein that the CDC and its partners are actually facilitating the creation of diseases and genocide; not the protection of public health, as this guide purports.
The intentional creation of diseases is being done by 2 primary mechanisms:
As stated in Harrison's Principles of Internal Medicine, 6th edition, p. 943: "RARELY IS PREVENTION OF INFECTION PER SE CONSIDERED TO BE AN IMPORTANT GOAL OF VACCINATION. In fact, asymptomatic infection after vaccination can serve to enhance and prolong the immune response." Of course, if the immune response has been overwhelmed or corrupted, the "asymptomatic infection" will become a CHRONIC DISEASE. In fact, on the same page of Harrison's, in the following paragraph, it states the following:
"PERSISTENCE AND LATENCY. Many viruses persist in host tissues for months or years without causing overt disease. A FLARE-UP OF THESE LATENT INFECTIONS MAY BE INDUCED BY TRAUMA, INTERCURRENT DISEASE, DECLINE IN ANTIBODY TITERS, OR UNKNOWN STIMULI. Experiments with tissue cultures and laboratory animals reveal that persistence of virus in tissue results from an interplay of various factors peculiar to each virus and its host. LATENCY IS PROMOTED BY THE PRESENCE OF ANTIBODY OR OTHER VIRAL INHIBITORS THAT PREVENT EXTENSIVE CELL-TO-CELL SPREAD OF VIRUS. IF ANTIBODY IS WITHDRAWN, VIRAL MULTIPLICATION OFTEN RESUMES, WITH CONCOMITANT CELLULAR NECROSIS."
In the same (6th) Edition of Harrison's Principles of Internal Medicine, it is stated on page 975 in regards to the poliomyelitis vaccine: "Vaccine virus multiplies in the intestinal tract and remains at this site. LIVE VACCINE VIRUS SPREADS AND INFECTS CONTACTS OF VACCINATED INDIVIDUALS. This type of immunization in the presence of epidemic poliomyelitis may lead to REPLACEMENT OF THE "WILD" PARALYTOGENIC STRAIN BY THE ONE IN THE VACCINE....." In direct contradiction to this statement, the 1/1/2000 Vaccine Information statement put out by the U.S. Department of Health & Human Services, Centers for Disease Control and Prevention National Immunization Program states that the "OPV (Oral Polio Vaccine) is better at keeping the disease from spreading to other People. However, it does state in this document that "OPV actually causes polio".
The inoculation of organisms causes disease both by direct introduction of organisms (including viruses that cause cancer) into the bloodstream, as well as corruption of the immune system leading to autoimmune disease (as can be read about on the CDC's own website, OCSO - OPHR - CDC's Research Agenda - Starter List Comments , where Dr. Carley's paper "Inoculation the True Weapons of Mass Destruction causing an Epidemic of Genocide" is posted, and describes the mechanism whereby corruption of the immune system occurs). In this paper (which Dr. William Atkinson of the CDC's immunization program has refused to respond to), it states that the hyperactivity of the humeral arm of the immune system in autoimmune disease is caused by adjuvants added just for that purpose. However, the damage caused by the autoimmunity (i.e., antibody against self) has several mechanisms, including the following:
For example, SUB ACUTE SCLEROSING PAN ENCEPHALITIS (SSPE) has been changed to AUTISM, as is demonstrated in the 10th edition of Harrison's Principles of Internal Medicine where, on page 2096, the following information about SSPE is included:
"...The disease affects boys 3 to 10 times as frequently as girls...Characteristically, they are entirely well until the disease begins. The onset of usually insidious mental deterioration, often expressed by a decline in the patient's schoolwork, is the presenting symptom . Incoordination, ataxia, and myoclonic jerks develop within a few months along with abnormalities of the pyramidal and extrapyramidal motor systems....Elevated levels of measles antibody are found in the serum and CSF....Measles virus is the etiologic agent....Staining of brain tissue from patients with the disease demonstrates measles virus antigen in the inclusions....A few reported cases have been related to measles vaccination." Of course, the vaccine etiology has been deleted from the 16th edition of Harrison's Principles of Internal Medicine, although the age of onset has been changed to 2 years in that edition.
What becomes SELF EVIDENT from these various editions of Harrison's Principles of Internal Medicine (the "Bible" by which all medical students learn about internal medicine) is that the source of almost all of the viruses that cause demyelinating diseases is actually VACCINES; and that the names of the diseases are changed to hide the true etiology. Another example of this can be found on page 2104 of the 10th edition of Harrison's Principles of Internal Medicine, under the discussion of ACUTE NECROTIZING HEMORRHAGIC ENCEPHALOMYELITIS, which is described as a "tissue destructive disease of the central nervous system which occurs with explosive suddenness within a few days of an upper respiratory infection. The pathologic findings are distinctive. On sectioning the brain, much of the white matter of one or both hemispheres is seen to be destroyed almost to the point of liquefaction. The involved tissue is pink or yellowish-gray and flecked with multiple small hemorrhages. Sometimes similar changes are localized to the brainstem or spinal cord. As in acute disseminated encephalomyelitis in showing perivenular foci of demyelination, all of like age.....The cerebrospinal fluid examination discloses a more intense reaction than in other demyelinating diseases....The etiology of this disease is not established; however, the entire clinical-pathologic entity bears a close resemblance to a hyper acute form of EAE which can be induced in animals by administration of endotoxin, PERTUSSIS VACCINE, or its histamine sensitizing factor coincident with or shortly after injection of myelin in adjuvant. What is self evident from this description is that this disease is actually SIDS (Sudden Infant Death Syndrome) or many of the cases of Shaken Baby Syndrome (the differentiation being whether the child has any evidence of trauma that the prosecutor can use to make a case for shaken baby and subsequently charge a parent with murder, as happened in the well-known case of Alan Yurko in Florida). Thus, once again, the name of the disease has been changed to conceal the fact that the pertussis vaccine is the cause of SIDS and many cases of Shaken Baby Syndrome.
In fact, after reviewing these 3 editions (6th, 10th, and 16th) of Harrison's Principles of Internal Medicine I conclude that most of the viral and demyelinating diseases of the central nervous system are, in fact, VIDS (Vaccine Induced Disease Syndromes). A very revealing statement making this truth self evident can be found in the Scope publications published by the Upjohn company and given to medical students; in particular, the 1983 edition of "Virology" which, on page 46 states the following under "Viral Pathogenesis": "Of a variety of possible portals of entry, the most common are inhalation, ingestion, direct contact with infected material, and direct injection by insect vectors". I invite any CDC official, immunologist, pediatrician or vaccination promoter to explain to the public how the amount of virus injected by the stinger of a mosquito is more dangerous to the public than the amount of virus contained in the hypodermic needle of a white coat. Additionally in this same edition of "Virology, on p. 47, the following is stated: "If a young pig infected intranasally with pseudo-rabies virus is added to a colony of uninfected animals, 80% to 90% of the pigs will become infected....Generally, injecting virus into a host produces infection more efficiently and with less virus than exposing the host to an infected animal." Once again, I invite any CDC official, immunologist, pediatrician or vaccination promoter to explain to the public how the same principle does not apply in the case of viruses that are put in a bottle and named "vaccines" to be injected, or inhaled (as in the case of "Flumist").
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, the CDC is promoting the development of even more vaccines, knowing full well the damage they are causing. In fact, the evidence shows that the CDC is involved in creation of viruses that cause cancer. As reported in Progress Report # 9 of the "Special Virus Cancer Program" (SVCP) run by the National Institutes of Health, the CDC, under grant VCL-42 (page 172 of progress report #9), the CDC investigator procured a total of 35 cell lines from leukemia and lymphoma cases (including 2 cases where the cancers were sexually transmitted to the spouse), and supplied these to several other investigators with the purpose of identifying a human tumor virus. This 396 page report identifies investigators in every major university, multiple pharmaceutical companies, veterinary colleges, zoos, and multiple federal agencies doing research to produce cancer causing viruses, testing factors to activate tumor formation in normal cells (including the use of latent viruses and activation of oncogenes), studying cancer formation after inoculation and intranasal transmission of cancer causing viruses, etc. This program also involved Merck and Dr. Maurice Hilleman, (touted as THE vaccinologist of the 20th century in his obituary in April 2005) whose project purported to investigate the development of vaccines to prevent cancers of viral etiology.
However, in 1962 Dr. Hilleman joked that the Russians would be no threat in the 1962 Olympics as they would be dragging with tumors caused by the SV 40 virus present in polio vaccines (note that the SV40 virus is a DNA plasmid of rhesus monkey origin being studied in many of the projects of the SVCP). The fact that, according to the Physician's Desk Reference, NO vaccine has ever been tested for its cancer causing potential is troubling enough. However, when US Code, Title 50, Chapter 32, Section 1520 & 1524 are considered (which state the Department of Defense can experiment on any American without their consent with biological warfare agents, including by use of vaccines (in violation of the Nuremberg code), in combination with transcripts of July 1, 1969 hearings before a subcommittee of the Committee on Appropriations of the House of Representatives (p. 129), the genocidal intention of these traitors to America becomes self evident. In these hearings (which evolved from directives issued by National Security Advisor Henry Kissinger just prior to issuing his most extensive depopulation report - National Security Memorandum 200), Dr. MacArthur states: "Within the next 5 to 10 years, it would probably be possible to make a new infective microorganism which could differ in certain important aspects from any known disease-causing organisms. Most important of these is that it might be refractory to the immunological and therapeutic processes upon which we depend to maintain our relative freedom from infectious disease". These biological agents created were obviously HIV/Aids, and the evidence points to this agent being spread via the use of inoculations.
Additionally, as reported in "Lab 257: The Disturbing Story of the Government's Secret Plum Island Germ Laboratory", on p. 219-221, author Michael Christopher Carroll states the following: Dr. David Huxsoll, who served on three U.N. biological warfare inspection teams in Iraq, and who was appointed as Plum Island's director in June of 2000, stated: "The plant that would produce biological agents for weapons purposes may not look too much different from the plant that produces biological agents for vaccine purposes....in the case of biological agents, you can disseminate them in an aerosol, and if you are good at this, you can spread them over a huge distance". This book discusses Plum Island as the likely origin of Lymes Disease, which the CDC has identified as a potential bioterrorism agent. THIS IS BUT ONE EXAMPLE OF THE BIOTERRORISM UPON THE AMERICAN PEOPLE BY AGENCIES AND CONTRACTORS OF THE US GOVERNMENT.
CONCLUSION: THE EMERGING VIRUSES AND OTHER BIOWARFARE AGENTS ARE EMERGING FROM GOVERNMENT FUNDED LABORATORIES; THE INTENTIONAL EXPOSURE OF THE AMERICAN PEOPLE TO THESE AGENTS VIA AEROSOLS (Chemtrails) AND INOCULATIONS CONSTITUTES GENOCIDE AGAINST THE AMERICAN PEOPLE, AND TREASON BY ALL PUBLIC OFFICIALS WHO ARE AIDING AND ABETTING THIS CONSPIRACY.
Besides population reduction, the financial motivation for these policies is crystal clear. As reported by John Hoey, M.D.:
In Service to the TRUTH, I AM,
Rebecca Carley, MD