THE MMR VACCINE IS DIRECTLY LINKED TO THE FOLLOWING TOXIC MANIFESTIONS WHEN INJECTED INTO THE HUMAN BODY - 1. MEASLES INCLUSION BODY ENCEPHALITIS Characterized by a ‘persistent measles virus infection, causing inflammation in both the white and gray matter and characterized by the presence of nuclear inclusion bodies We report a case of measles inclusion-body encephalitis (MIBE) occurring in an apparently healthy 21-month-old boy 8.5 months after measles-mumps-rubella vaccination. He had no prior evidence of immune deficiency and no history of measles exposure or clinical disease. Note: ‘The presence of measles virus in the brain tissue was confirmed by reverse transcription polymerase chain reaction. Clinical Infectious Diseases 1999 Oct;29(4):855-61 Official Package Insert: ‘M-M-R II is a sterile lyophilized preparation of (1) ATTENUVAX* (Measles Virus Vaccine Live), a more attenuated line of measles virus, derived from Enders’ attenuated Edmonston strain and propagated in chick embryo cell culture; (2) MUMPSVAX* (Mumps Virus Vaccine Live), the Jeryl Lynn** (B level) strain of mumps virus propagated in chick embryo cell culture; and (3) MERUVAX* II (Rubella Virus Vaccine Live), the Wistar RA 27/3 strain of live attenuated rubella virus propagated in WI-38 human diploid lung fibroblasts.’ Note: Aborted Fetal Tissue is laced in the Rubella portion of the formula - ‘strain of live attenuated rubella virus propagated in WI-38 human diploid lung fibroblasts (Aborted Fetal Tissue).‘ WI-38 came from lung cells from a female fetus of 3-months (terminated during the 1st Trimester/United States 1961) gestation: ‘Minced preparations were obtained by cutting the tissue in a Petri dish containing GM (growth medium) with paired scalpels or a scissors until the size of each piece approximated l-4 mm3. Fragmented preparations were obtained by tearing apart the tissue with two pairs of forceps in a Petri dish containing GM until the pieces could no longer conveniently be grasped and shredded. The entire contents of the dish were emptied into one or more Pyrex Blake bottles (surface area 100 cmZ), depending on the size of the original starting tissue. The fragmented lungs, for example, from a three-month-old human fetus were usually placed in four Blake bottles. Treatment of tissue with trypsin was done, in general, according to the method of Fernandes.’ ‘The WI-38 and MRC-5 cell cultures have been used to prepare hundreds of millions of doses of (following) vaccines – rubella (third compontent of the MMR series, administered in 2 doses, first at 12 months old), hepatitis A (administered in 2 doses, first at 12 months old), varicella (chichenpox, administered in 2 doses, first at 12 months old) and rabies (administered selectively pending rabies-related emergency).‘ National Network for Immunization Information 2. MUTAGENIC (WEAPONIZED) HYBRID OF MEASLES The MMR Vaccine has co-infected an entire generation of children with a more virulent strain of Measles, now referred to as Atypical measles (AMS). The Medical Industry has reluctantly confirmed this vaccine-derived mutation circulating throughout the environment: ‘Atypical measles occurred (occurs) in children who received formalin-inactivated (killed) measles vaccine that was in use in the United States from 1963 to 1968. These children developed high fever, a rash that was most prominent on the extremities and often included petechiae, and a high rate of pneumonitis. Recent studies in monkeys indicate that this illness was caused by antigen-antibody immune complexes resulting from incomplete maturation of the antibody response to the vaccine.‘ The Journal of Infectious Diseases ‘Atypical measles can occur in people who were immunized with a killed virus vaccine that was used from 1963-1967 and then exposed to the original virus. It can also occur in people who were immunized with the current vaccine but, for some reason, failed to develop immunity, and in people who are immunosuppressed.‘ Note: ‘The symptoms of atypical measles are different and more severe than the symptoms of typical measles.‘ Symptoms of Vaccine-derived hybrid strain of Measles (Atypical Measles/AMS): A. Maculopapular ‘characterised by flat spots (macules) and tiny bumps (papules) on the surface of a tissue—usually understood to mean the skin or an organ (e.g., the liver or spleen).’ B. Petechial ‘pertaining to tiny red or purple spots caused by an extravasation of blood into the skin.’ C. Vesicular ‘composed of or relating to small, saclike bodies.’ D. Urticarial ‘hives; a vascular reaction of the upper dermis marked by transient appearance of slightly elevated patches (wheals) which are redder or paler than the surrounding skin and often attended by severe itching.’ 3. SIMIAN VIRUS 40 (SV40) ‘Mutations and minority variants, relative to vaccine strains, not known to affect attenuation were detected in OPV, mumps virus, and varicella-zoster virus. The anticipated detection of endogenous retroviral sequences from the producer avian and primate cells was confirmed. Avian leukosis virus (ALV), previously shown to be noninfectious for humans, was present as RNA in viral particles, while simian retrovirus (SRV) was present as genetically defective DNA.’ Journal of Virology, June 2010 vol. 84 no. 12 Note: ‘simian retrovirus (SRV) was present as genetically defective DNA.‘ A growing number of children with Autism are now potentially cross-infected with SV40 (diseased African Green Monkey kidney derived Polio virus) type hybrid strains of Poliomavirus (67% infection with Simian Virus); based on a recent Controlled Study which found poliomavirus infection in post-mortem brains of sufferers of Autism – inevitably the result of inter-generational cross-contamination from Salk & Sabin Polio inoculations, sugar cube/oral drops versions & the subsequent Inactivated Polio Vaccine now on the schedule; fixed in the germ line DNA of babies/children. ‘BKV (BK Virus- human polyomavirus that causes widespread infection in childhood and remains latent in the host), JCV (JC Virus -type of human polyomavirus or papovavirus), and SV40 (Simian Virus 40) combined are significantly more frequent among autistic patients compared to controls (67% versus 23%, respectively; P
Posted on: Wed, 16 Apr 2014 15:09:57 +0000