The Hidden Results of Human Vaccinations
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_i d=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, longrange 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: 1. Genetic engineering of organisms (especially viruses which cause cancer under the "Special Virus Cancer Project", as detailed below), as well as 2. Inoculation of organisms via the practice touted as "vaccination". The definition of these words makes the truth self evident. As defined in Dorland's Medical Dictionary, 25th edition: p. 1685 - "vaccinate" = to inject vaccine for the purpose of inducing immunity p. 784 - "inoculate" = to communicate a disease by inserting its etiologic agent
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:
1. 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. causing DEMYELINATION. 2. 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) causing DEMYELINATION (leading to Autism, as proven below). In the aforementioned 6th edition of Harrison's Principles of Internal Medicine on p. 1791, under the heading "Multiple Sclerosis and other DEMYELINATING Diseases", it states the following: "A large and important group of neurologic disorders are termed the demyelinating diseases because they share the common pathologic feature of foci of degeneration, involving the myelin sheath of nerves. These foci vary in size, shape, distribution, and rate of development in the different illnesses. The axis cylinder often suffers damage, as does the myelin sheath, but the destruction of myelin is considered the primary change...syndromes can be clearly distinguished....(including) acute disseminated encephalomyelitis (including post infectious and POSTVACCINAL ENCEPHALOMYELITIS)...(P. 1798) - "the association of the neurologic disorder with vaccination or inoculation usually leaves the diagnosis in little doubt, and the characteristic combination of encephalitic and myelitic features will help to distinguish the condition from meningitis, viral encephalitis, and poliomyelitis". This self evident fact has been taken out of subsequent
editions of Harrison's Principles of Internal Medicine , since as the vaccine schedule has dramatically increased over the years, the incidence of vaccine induced demyelination has correspondingly increased. This is most evident in the case of autism, which has now risen to epidemic proportions in this country. Yet, whereas there is almost no history of the disease in the families of these children in most cases, and the parents report the onset of symptoms after the child receives the MMR vaccine, the various arms of the medical establishment (including the CDC) conclude that this is just a "coincidence"; rather than that the association of the neurologic disorder (autism) with vaccination or inoculation usually leaves the diagnosis in little doubt. The way that the true etiology of autism is hidden from doctors is by changing the name of the vaccine induced disease. 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
