Sunday, June 24th., 2018
"...Notice at minute 6:20 “The Brain and Immune System are Linked at birth”..."
Bombshell Interview: Biochemist Says ‘Ton of Data’ Proves Vaccines Plays Major Role in Autism (Video)
06/23/2018(Circle of Docs) Shocking
Interview With Dr. Judy Mikovits PhD on Vaccines, Autism, Chronic
Illness and The Billion Dollar Corruption That Surrounds It All
Related Retroviruses Contaminate the World’s Vaccine Supply for Pets & Humans, Research Suggests
Source – The Millennium Report
by Circle of Docs, December 2nd, 2015
This is the most shocking & damming interview we have watched regarding vaccine injury.
This is a Periscope video from CDC Whistleblower Candyce Estave.
Dr Judy Mikovits,
PhD is a Biochemist, cellular and molecular biologist with over 30
years of scientific expertise. She has directed programs on HIV, cancer,
epigenetics, and neuroimmune disease, with a focus on development of
novel drug and diagnostic technologies. She is an award winning book
called Plague.
Dr. Mikovits holds a PhD in Biochemistry and Molecular Biology from
George Washington University. Her dissertation was on HIV latency and
mechanisms of immune activation in monocytes. Dr. Mikovits was a
Postdoctoral Scholar in Molecular Virology at the Laboratory of Genomic
Diversity, National Cancer Institute under Dr. David Derse.
Over the past 26 years, she has published 51 scientific papers in
peer-reviewed journals, and worked as a government scientist for many
years developing viruses and vaccinations. In 2011 when she made a
horrifying discovery that was contaminating all vaccinations, she
presented her data to government officials and was threatened & told
to destroy all her data.
When she was jailed, her career systematically destroyed, and
a gag order put in place for 4 years threatening that if she spoke out
she would be thrown back in jail. That gag order has just lifted, and she’s dumped the government right in it!
She speaks in this interview with Candyce Estave about how autism is
associated with vaccines, also cancers, chronic fatigue syndrome,
Alzheimers, auto immune diseases, allergies and more.
Buy Book Dissolving Illusions — Debunking Vaccination History with Real Science
Notice at minute 6:20 “The Brain and Immune System are Linked at birth”
She discusses how the cocktail of vaccinations pumped into babies
mutate to develop months and years down the track into new viruses,
cancers and diseases, some they don’t even know about yet.
She further explains how the viruses injected through vaccines tear
open our DNA and insert their own DNA to mutate our genetic makeup and
be passed on generation after generation.
Here is some of the research she has studied and references in this interview:
1. Antipurinergic Therapy Corrects the Autism-Like Features in the Poly (IC) Mouse Model – In early 2013, Dr. Robert Naviaux, a Professor of
Genetics and co-director of the Mitochondrial and Metabolomic Disease
Center at the University of California, San Diego, as well as the
recipient of an Autism Speaks International Trailblazer award reported some of the most exciting autism news in years. In an article published inScience Daily on
March 13, 2013, Naviaux explained, “When cells are exposed to classical
forms of danger, such as a virus, infection, or toxic environmental
substance, a defense mechanism is activated. This results in changes to
metabolism and gene expression, and reduces the communication between
neighboring cells. Simply put, when cells stop talking to each other,
children stop talking.” In PLOSOne Naviaux and his team reported that
administration of an old drug, suramin, (traditionally used to treat the
parasite which causes African sleeping sickness) restored cell to cell
communication in a mouse model of autism, raising hopes that a similar
result might be obtained in humans. http://www.sciencedaily.com/releases/2013/03/130313182019.htm http://www.ncbi.nlm.nih.gov/pubmed/23516405
2. War and Peace between Microbes: HIV-1 Interactions with Coinfecting Viruses – This 2009 article from the Journal Cell Host and Microbe explains
how a retrovirus can disrupt the equilibrium between a host and its
microbes, resulting in a reactivation of persistent viruses, or invasion
by new viruses, as well as resulting in either immuno-deficiency or
immuno-activation.
3. Generation of Multiple Replication-Competent Retroviruses through Recombination between PreXMRV-1 and PreXMRV-2 –
This research from Dr. John Coffin and Dr. Vinay Pathak showed that
replication competent murine leukemia retroviruses can be produced in a
relatively short period of time. From their abstract, “To determine
their potential to generate RCRs (author’s note – replication-competent
retroviruses), we transfected PreXMRV-1 and PreXMRV-2 into 293T cells
and used the virus produced to infect fresh cells; the presence of
reverse transcriptase activity at 10 days indicated the presence of
RCRs.” http://www.ncbi.nlm.nih.gov/pubmed/23966380
4. Frequent Detection of Infectious Xenotropic Murine Leukemia Virus (XMLV) in Human Cultures Established from Mouse Xenografts –
This chilling research from the well-regarded Dr. Adi Gazdar, suggests
that the murine leukemia retroviruses may have the potential to become
airborne. In their conclusion the Gazdar team warned, “Laboratories
working with xenograft-derived human cultures should be aware of the
risk of contamination with potentially bio-hazardous human-tropic mouse
viruses and their spread to other cultures.” http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3218386/
5. Xenotropic Murine Leukemia Virus-related Virus-associated Chronic Fatigue Syndrome Reveals a Distinct Inflammatory Signature – (The cytokine signature paper was published in 2010 and first presented in CFS patients at IiME in London in 2008). This
research by PLAGUE co-author, Dr. Judy A. Mikovits, was the first to
identify a signature of 10 cytokines and chemokines which would
correctly identify XMRV/CFS patients with a 93% specificity and 96%
sensitivity. http://www.ncbi.nlm.nih.gov/pubmed/21576403
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6. Xenotropic MLV Envelope Proteins Induce Tumor Cells to Secrete Factors that Promote the Formation of Immature Blood Vessels –
This 2013 research by Dr. Gary Owens of the University of Virginia
provides evidence that envelope proteins on the surface of murine
leukemia viruses can affect cancer progression. The article states,
“The studies described herein address these questions, and show that at
least one other XMRV-like virus exists, and that the virus evolved the
ability to infect human cells and to express gene products that impact
tumor pathogenesis.” Dr. Mikovits will never forget how even at the
XMRV Conference held at the Cleveland Clinic in November of 2009, Dr.
Owens was asserting that more than one type of xenotropic murine
leukemia virus might exist, as is the case with other known human
retroviruses. Dr. Mikovits will also always remember the kindness with
which Dr. Owens invited her to a series of lectures timed to coincide
with the 30th anniversary of her graduation from the University of
Virginia. http://www.ncbi.nlm.nih.gov/pubmed/23537062
7. Neurotoxic Effects of Postnatal Thimerosal are Mouse Strain Dependent –
This work from Dr. Ian Lipkin and Dr. Mady Hornig was the first to
demonstrate that auto-immune sensitive mice had a decreased ability to
handle the hazard posed by mercurials used in common childhood vaccines
and developed behaviors reminiscent of autism. PLAGUE co-author, Kent
Heckenlively would like to express his appreciation for Dr. Ian Lipkin’s
kind invitation to attend a cocktail reception on September 19, 2013 at
the SoHo Grand Hotel in Manhattan, honoring the work of Columbia
University in chronic fatigue syndrome/ME and autism. At the event Kent
especially enjoyed a series of delightful conversations with the
brilliant, brave, and engaging Dr. Mady Hornig about her research. http://www.ncbi.nlm.nih.gov/pubmed/15184908
8. Identification, Viral Dissemination and Antibody Responses of Rhesus Macaques Exposed to the Human Gammaretrovirus XMRV –
This research from Emory University showed that murine leukemia viruses
tend to disappear quickly from the blood, settling in specific organs,
but can easily be reactivated by immune stimulation. http://jvi.asm.org/content/early/2011/02/16/JVI.02411-10.abstract
9. The Rise in Autism and the Role of Age at Diagnosis – This 2009 article from the journalEpidemiology by
Dr. Irva Hertz-Picciotto of the MIND Institute of the University of
California, Davis tracked autism cases identified in California from
1990-2006. Picciotto and her team found that the rate of autism
increased from a rate of approximately 1 in every 1,600 births in 1991
to a rate of approximately 1 in every 235 births in 2001 and the
increase showed no signs of slowing. In April of 2013 the CDC reported
that the estimated rate of autism is now 1 in every 50 births. In an
article published in Scientific American on January 9, 2009,
Dr. Hertz-Picciotto noted that while several studies had suggested the
increase in autism was due to increasing chemical exposures, “In
addition, fetuses and infants might be exposed to a fairly new
infectious microbe, such as a virus or bacterium, that could be altering
the immune system or brain structure.” http://journals.lww.com/epidem/Abstract/2009/01000/The_Rise_in_Autism_and_the_Role_of_Age_at.16.aspx
10. The Exotic Biology of Xenotropic Murine Leukemia Related Viruses: Pitfalls and New Concepts –
This presentation from Dr. Judy A. Mikovits at the Mount Sinai
Conference in November of 2013 details the very latest findings on the
exotic biology of the murine leukemia retroviruses and the role they may
play in many human diseases. (44 slides): https://www.facebook.com/media/set/?set=a.244564049033185.1073741854.101589063330685&type=1
11. Evaluation of the Broad-Range
PCR-Electrospray Ionization Mass Spectrometry (PCR/ESI-MS) System and
Virus Microarrays for Virus Detection – This
research from the University of California, Berkeley, and the Food and
Drug Administration (as well as a very significant assist from Dr.
Crystal Jaing of the Lawrence-Livermore National Laboratories)
illuminates the best practices for viral detection and some unsuspected
dangers.
From the conclusions section, “In addition to the LOD
studies, we used the new virus detection methods to analyze some
vaccine-related cell substrates for the presence of novel viruses. Total
nucleic acids were used for the detection of both DNA and RNA viruses.
Analysis of cell lines by PLEX-ID and virus microarrays indicated the
presence of various retrovirus-related sequences. However, the origin of
these sequences could be attributed to the presence of cellular DNA
containing endogenous retroviral sequences or viral transcripts that may
be expressed constitutively from some endogenous retroviral DNAs
(proviruses). However, this situation is applicable to all nucleic
acid-based assays that can detect retroviruses. To assess the origin and
nature of the retroviral sequences a follow up strategy using PCR,
sequencing, and bioinformatics was developed. The analysis revealed that
the unexpected RD114 sequences detected by PLEX-ID in canine cell lines
were associated with endogenous gammaretroviruses . . . Our analysis
showed that different viruses were detected by using different
technologies. These results emphasize the need to use a combination
strategy for virus detection in evaluating the safety of biologicals or
screening patient samples.”
This research strongly supports a combination strategy to
detect novel viruses in biological products like the cell substrates
used in vaccines as well as when investigating suspect disease
populations who may be suffering from some type of viral infection. http://www.mdpi.com/1999-4915/6/5/1876/htm
12. How Can Xenotropic Murine Leukemia Virus-Related Virus (XMRV) Contamination be Prevented? –
This article published in February of 2014 in the journal of the
American Society of Microbiology addresses the question of how to
prevent both laboratory contamination by XMRV as well as prevent the
infection of lab workers. The article describes XMRV as a lab creation
which is capable of “infecting human cells and integrating its genome
into that of the host. Therefore, XMRV virions and XMRV-infected cells
are considered as biosafety level 2 organisms.” http://aem.asm.org/content/early/2014/02/10/AEM.04064-13.abstract
13. Origins of the Endogenous and Infectious Laboratory Mouse Gammaretroviruses –
Successful interspecies transmissions can produce disease in new hosts
that are unprepared to resist unfamiliar and potentially pathogenic
agents. Xenotropic MuLVs (X-MuLVs) were later isolated by Levy and
Pincus from the NZB mouse strain [2], and were termed “xenotropic”
because they could infect cells of multiple species, such as human,
rabbit and cat, but were unable to infect cells of the mice from which
they were isolated. While these early observations suggested that
P-MuLVs have the broadest host range of the MuLV subgroups, more recent
studies have shown that X-MuLVs can actually infect more mammalian
species than P-MuLVs, and that X-MuLVs but not P-MuLVs are capable of
infecting all wild mouse taxa [8] (Table 1).http://www.mdpi.com/1999-4915/7/1
___
https://circleofdocs.com/shocking-interview-with-dr-judy-mikovits-phd-on-vaccines-autism-chronic-illness-and-the-billion-dollar-corruption-that-surrounds-it-all/
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Source:
http://themillenniumreport.com/2018/06/bombshell-interview-biochemist-says-ton-of-data-proves-vaccines-plays-major-role-in-autism-video/
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