Dr. Wakefield's Crucifixtion
Dr. Wakefield's crucifixtion is a desperate well-orchestrated effort to restore faith in risky vaccinations that the majority of people worldwide no longer trust -Dr. Len Horowitz
The headlines blasted around the world vilifying Dr. Wakefield should instead have been trumpeting the success enjoyed by the team of doctors at the Royal Free Hospital in London, the families of the kids who participated, and certainly the children themselves, when the treatments for their inflamed bowels resulted in amelioration of their symptoms of autism. When kids who hadn't been able to sleep through the night for months began getting a full night's sleep. When kids who hadn't spoken for months - or longer - again began speaking, and speaking at a level commensurate with their age at the time, not at the age at which they'd stopped speaking; thus demonstrating continued mental growth despite the outward appearance of absence. And kids who'd lost emotional connection with their families once again recognized and bonded with their parents and siblings.
Co-Author of Lancet MMR-Autism Study Exonerated on All Charges of Professional Misconduct
A few years after Dr Wakefield found vaccine-strain measles virus in the gut of measles-vaccinated children with autism and bowel disease, US autism researcher Dr Jeff Bradstreet presented evidence to the Institute of Medicine in Washington showing vaccine-strain measles virus in the cerebral-spinal fluid of three children with autism and bowel disease. That most definitely should not be in central nervous system, however we know that surfactants in vaccines can breech the blood brain barrier, allowing vaccine ingredients to gain access to the CNS; a likely cause of SIDS. Dr Bradstreet's office was then raided by the FDA, and a few days later his body was found in a river with a gunshot wound to the chest. Authorities are calling the incident a suicide. Full article: The Daily Mail
35 Peer-Reviewed Research Papers Supporting Dr Wakefield's Findings
It's no wonder the British government tried to discredit Dr Wakefield's research by any means possible. He, along with 12 other MDs participating in the study, had found a link between the MMR vaccine and inflammatory bowel disease in 12 autistic children. When the children's bowel disease was treated with conventional anti-inflammatory drugs, such as those used for Crones disease, the children's bowels recovered, and they started speaking again! Because the government had already given the vaccine makers immunity from liability for any vaccine injury, it would have been the government who would have been sued by parents of the damaged children. That's why there was the massive effort to discredit Dr Wakefield in any way possible. They recruited a journalist (with no medical training) to perpetuate false accusations in the press, pressured the Lancet to withdraw his paper, and pressured the U.K. medical licensing body to revoke his license to practice medicine. The Lancet even refused to publish another paper of his, totally unrelated to his MMR study, in which Dr Wakefield showed that infant chimps given the Hep B vaccine showed a delay in the ability to "latch" for breast-feeding, compared to a control group.
People who believe the lie that Dr Wakefield's study was "debunked" need to read the scores of studies that affirm his research:
New study from UC Davis: Immune System and Gastrointestinal Deregulation Linked with Autism
35 peer-reviewed papers supporting the findings of the original work by Dr Wakefield and colleagues.
157 Research Papers Supporting the Vaccine/Autism Link
Andrew Wakefield's Study Co-Author Completely Exonerated by British Court
Below, watch "Hear The Silence", a professionally produced, made for television dramatization of what really happened with Dr. Wakefield and the parents who inspired his research.
NIH Admits MMR Vaccine Can Cause Acute Disseminated Encephalomyelitis (ADEM)
According National Institute of Health (NIH), acute disseminated encephalomyelitis (ADEM) is "characterized by a brief but widespread attack of inflammation in the brain and spinal cord that damages myelin, the protective covering of nerve fibers. ADEM often follows viral or bacterial infections, or less often, vaccination for measles, mumps, or rubella."
Also, UK government documents show MMR vaccine can cause Subacute Sclerosing Panencephalitis. SSPE is a degenerative neurological condition, which affects a person's behavior, memory and coordination, leading to fits, siezures, blindness and eventually death from fever, heart failure, or their brain's inability to continue controlling the autonomic nervous system.
Dr Wakefield's 1998 Research Proven Correct
March 8, 2013: Dr Wakefield's 1998 research proven correct by new study led by Dr Krigsman at Wake Forest University: MMR Vaccine Causes Autism & Inflammatory Bowel Disease. How many children have been disabled by the MMR vaccine in the 15 years since his 1998 report? For articles supporting Dr Wakefield's research, see Callous Disregard.
June 25, 2013: Science Daily: Dramatic Increase in Hospitalization of US Children With Inflammatory Bowel Disease
2002 USU Study: Pubmed: Abnormal measles-mumps-rubella antibodies and CNS autoimmunity in children with autism
2002 BMJ Study: Pubmed: Potential viral pathogenic mechanism for new variant inflammatory bowel disease
William R. Long, PhD, JD: On Second Looking into the Case Of Dr. Andrew J. Wakefield
Nov 29, 2016 Study: Molecular Autism: Alterations in blood-brain barrier and intestinal permeability in ASD Press release/summary Abstract and details of study methods
Oct 3, 2017: San Francisco Chronicle: NIH Grant Funds Researchers Exploring Link Between Gut Bacteria and Autism
Two Dozen Peer Reviewed Studies on the Vaccine-Autism Link plus links to 100 relevant articles.
Vaccines are Causing an Unprecedented Number of Mutations
The MMR, DTaP and some flu shots contain Neomycin. Neomycin destroys gut bacteria (good and bad), which allows pathogens to take over and weaken the immune system. When the immune system is destroyed or weakened, pathogens can take hold. When you kill the Alpha pathogen that was keeping a pack of lesser bugs under control, you unleash a Pandora's Box of mutated strains, and the formerly lesser pathogens become increasingly virulent. The shots also contain Polysorbate 80, which degrades (makes permeable) the gut and blood brain barrier, allowing the vaccine contents to enter where they should not be. Source: Dave Mihalovic, ND Vaccines are Causing an Unprecedented Number of Mutations
IOM: The Evidence Convincingly Supports a Causal Relationship
Measles, Mumps, Rubella Vaccine (series) - 1st round given at 12-15 months old:
The evidence convincingly supports a causal relationship between MMR vaccine and measles inclusion body encephalitis in individuals with demonstrated immune deficiencies. P.110 Institute of Medicine Report on Adverse Effects of Vaccines/2011
Measles inclusion body encephalitis is characterized by 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. During hospitalization, a primary immunodeficiency characterized by a profoundly depressed CD8 cell count and dysgammaglobulinemia was demonstrated.
Note: The presence of measles virus in the brain tissue was confirmed by reverse transcription polymerase chain reaction. The nucleotide sequence in the nucleoprotein and fusion gene regions was identical to that of the Moraten and Schwarz vaccine strains; the fusion gene differed from known genotype A wild-type viruses. Clinical Infectious Diseases 1999 Oct; 29(4):855-61
MMR II Vaccine Contains Human DNA from Aborted Fetal Tissue
The MMR II vaccine is contaminated with human DNA from the cell line. This human DNA could be the cause of the spikes in incidence [of autism]. Journal of Immunotoxicology, 2011; 8(1): p 68-79
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 (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 WI-38 and MRC-5 cell cultures have been used to prepare hundreds of millions of doses of (following) vaccines rubella (third component 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 (chickenpox, administered in 2 doses, first at 12 months old) and rabies (administered selectively pending rabies-related emergency). National Network for Immunization Information
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
Could Hepatitis B Vaccine Be Harmful? by Sharyl Attkisson
October 7, 2009: In a newly-published study, vaccinated monkeys demonstrated "significant delays in the acquisition of critical survival reflexes" compared to an unvaccinated control group, reports CBS News correspondent Sharyl Attkisson.
It was the first time researchers had time compared vaccinated animals with unvaccinated controls. Researchers vaccinated 13 newborn rhesus macaque monkeys with Hepatitis B vaccine containing a standardized amount of thimerosal - a vaccine preservative thought by some to cause developmental issues. The thimerosal dose matched that given to human babies until the early 2000s. Four monkeys received a saline placebo and three more had no shots at all.
The study found the unvaccinated animals developed normally, while the vaccinated monkeys demonstrated an inability to latch for breast feeding, a crucial survival reflex. According to one of the lead investigators, Dr. Laura Hewitson of the University of Pittsburgh, "Infants of lower birth weight and gestational age were at greater risk."
The study, published last week in the scientific journal NeuroToxicology, was not designed to determine whether it was the thimerosal or another component of the vaccine that caused the observed delays.
"We undertook these experiments largely because we were unable to find any safety studies comparing vaccinated and unvaccinated animals," said another study author, Dr. Andrew Wakefield of Thoughtful House, which provides resources for children with developmental disorders. CBS News