The Threat of Fetal DNA In Vaccines


today I am only going to discuss the
real and present danger of having human fetal manufactured vaccines that can
trigger autoimmune reactions and gene mutations in our children that could
lead to very serious diseases this is a graph of receptors that are part of our
immune system they are called toll-like receptors the ability of the immune
system to recognize molecules that are shared by pathogens like bacteria or
viruses is in part due to the presence of these toll-like receptors that are
expressed on the membranes of leukocytes including dendritic cells macrophages
natural killer cells cells of the adaptive immunity T and B lymphocytes so
the toll-like receptors have been implicated in many human autoimmune
States and in particular I’m going to focus on toll-like receptor 9 when this
receptor is activated by what is called hypo methylated DNA the that activation
is associated with diseases that include lupus rheumatoid arthritis Crohn’s
disease multiple sclerosis systemic scleroderma psoriasis inflammatory bowel
disease type 1 diabetes Sjogren’s syndrome Myositis and I want
to emphasize encephalitis which is a brain inflammation so when viral or
primitive DNA fragments bind to toll-like receptor 7 or 9 it activates
both innate and adaptive in Yunis Ponce’s that will then be looking
to find the same or similar DNA anywhere else in the body so TL r9 has evolved as
a general innate immune sensor for viral DNA bacterial DNA fungal and protozoan
DNA and other DNA that is unmethylated in certain areas or primitive DNA what
other sources of hypo methylated DNA are there I’ve mentioned viruses cancer
cells can be a source of hypo or under methylated DNA the DNA in patients with
autoimmune diseases is often hypo or under methylated and fetal DNA is
primitive DNA which is also hypomethylated so what happens when this
I’m putting the wrong way when this hypo methylated DNA binds to the toll-like
receptor it’s on debt and it cells of the innate immune system and that
releases cytokines that sort of trigger a general immune response or revving of
the immune system BAE lymphocytes also have to–like receptor 9 and when the
toll-like receptor activates the b-cells antibodies are made and then those anti
bodies move through the bloodstream looking for the same or similar DNA to
eliminate it – kill it – kill the virus this receptor is actually how some
vaccines work like the chickenpox what’s what I want to show you is how important
this receptor can be this is actually back from 1980 1998 and what happens as
a baby grows what happens during pregnancy is the placenta begins to
break down and fetal DNA from the degrading placenta enters the mothers
bloodstream and when it reaches levels of about 0.2 to nanograms per mil so
later in labor it activates the toll-like receptor nine antibodies are
made to the baby’s DNA and they then travel through the bloodstream in this
case instead of killing a virus you get your baby okay so just to summarize DNA
viruses like chickenpox activate the toll-like receptor 9 that’s
how we get immunity when we’re given the vaccine and fetal DNA it enters the
mother’s blood stream also activates this receptor and causes labor okay so
just to a summary of the fetal DNA it’s hyper methylated it’s about 300
base pairs in luton fragment lengths and the this is plasma levels when it gets
above 0.46 that is 0.2 to nanograms in whole blood
it causes labor which is a very profound biologic immune response we are born
with more nerve cells than we have later in life and between births actually got
a few months of age and three years of age 90 percent of our nerve cells die so
this is just data from rats the black circles are a number of nerve cells and
you can see that there’s a very rapid dial and a one week old rat corresponds
to about a five months to a one and a half year old yeah so this slide is from
autopsy data from humans and you can see this very rapid nerve die-off in the
human that occurs from birth to two years of age so this is important
background if a child has been exposed to human fetal DNA they will have
antibodies to primitive hypo methylated DNA there are people with genetic
signatures that make them have hypo methylated DNA and if they have
antibodies to hypomethylated fetal DNA present when they undergo this brain
remodeling they can have a massive autoimmune attack not against their own
brain and so where would a child be exposed
human fetal DNA to make these antibodies and you’ve already heard from the
previous speakers that when vaccines are manufactured in human fetal cells they
are heavily contaminated with human fetal DNA fragments okay this is data
from my lab where we measured the amount and the size of the human fetal DNA on
average the MMR 2 contains about 200 nanograms so previously recommendations
were that the DNA be limited to 100 pika grams but those recommendations have
been raised twice and are now at 10 nanograms so I just want to emphasize
that this vaccine has a single-stranded and double stranded DNA close to 200
nanograms so 20 times over and a perfect size to activate the toll-like receptor
9 this is data from merck on the chickenpox vaccine and they report that
there are 2 micrograms of the human fetal DNA in each shot that we give our
children ok so just for some perspective micrograms are 1,000 times higher than
nanograms and this is actually from an Italian group who measured the levels in
Prior Xterra and there are 1.35 micrograms per vaccine the next two
slides are just typical high and wait slides for toddlers and I used
these tables to find out the typical weight of a child when they get their
vaccines and based on that there are algorithms that are available on the
computer that will tell you the child’s blood volume so um the bottom rows here
these are the levels of human fetal DNA that trigger labor in their mother which
is a very profound biologic response and up here are the contaminating amounts in
these three vaccines and these are the levels in the blood of our children when
they are typically vaccinated so this is about a six-month-old child this is
about one one-year-old child and you can see that all of these levels are above
the levels needed to trigger labor their scientists and the doctors who push
these vaccines claim that the human fetal contaminants they had knowledge
they are there are harmless but anyone who says that either does not know
anything about immunology or they are not telling the truth so I want to talk
a little bit about the other known danger of these fetal contaminants which
is a danger that they would insert into the child’s genome and cause mutations
and we know a lot about this from the field of gene therapy
so we’ll just so I’m going to just introduce you to what’s called small
fragment homologous recombination which is how we do gene therapy so for genes
fair a targeted DNA is synthesized to
specifically correct the mutation that a child has and small fragment homologous
recombination does not occur cross species so just for example when they
make vaccines in a chicken sell the chicken DNA is never going to insert
into your child’s dam and the the best DNA to insert by this homologous
recombination is hypo methylated DNA and the best DNA is between 50 and 1000 base
pairs in length and stem cells readily undergo small fragment homologous
recombination and so then I just want to reiterate what the vaccine contaminant
DNA is so this is a gel that is just looking at how this works and they’re
using placental DNA fragments okay so this is mutated gene this is the correct
gene you can see when they added these placental DNA fragments that the gene
has been corrected in in in in some some of the some of the cells okay so this
gel just shows you again gene correction and in this column they use the
placental DNA and they they get these bands again but if they use salmon
primitive DNA there’s no there’s no correction there’s no bands so we don’t
need to be afraid of cow DNA we’re never gonna grow tails okay okay so this is in
a mouse and they wanted to do this gene therapy in an animal and all of the
animals had this happen in their bone marrow and the cells that were changed
were hematopoietic stem cells and it was at a rate of 0.4 3 percent similar to
the levels of autism and development so the problem with having mutated stem
cells is that they can give rise to immune cells that will enter the brain
and not function normally so again this is just the concentrations of fetal DNA
in our children’s blood on the top and this is the concentration in the mouse
experiment 1.9 nanograms per mil and you can see that in several cases these
levels from vaccines are well over this level and any doctor or scientist who
claims that the contaminants are not going to do anything either doesn’t know
anything about gene therapy or they’re not telling the truth okay
so there’s quite a bit of real-life evidence of how dangerous these
mutations are this is from a clinical trial where they did gene therapy for
boys who lacked an immune system okay so they they took the blood from the boys
they isolated the stem cells and they did this small fragment recombination
and then they gave the stem cells back to the boys and nine of the boys were
cured okay so nine out of ten were cured for
developed acute lymphocytic leukemia and had to undergo chemotherapy and
and one of them died so they did wanted to understand how this happened so what
I’m showing you on this slide is this is when the cancer was first detected and I
want to point out that was 68 months historical they did the gene therapy and
in this child it was 33 months ok so the original insertion did not directly
cause the cancer okay so other scientists did more research and what
they found was that the gene the insertion occurs in areas of the DNA
that gives that stem cell of proliferation advantage and it also
causes other additional mutations that caused the cancer now the insertion
doesn’t always cause cancer because only four of the boys developed cancer so we
could have a cell with an insertion and a survival advantage that would be
abnormal and and yet not cancerous so the scientists in this trial concluded
that the Leukemia genesis was likely caused by other genetic abnormalities
and they highlighted the the general dangers of gene therapy so scientists
admit that this dear I could insert into a child cell but
they say it could only cause cancer not one of the chronic diseases that are so
epidemic like autism and they say that because they cannot conceive that an
abnormal stem cell I’m gonna impact an entire brain but the scientists who say
that either don’t know anything about gene therapy or they’re not telling the
truth and in many cases I think it’s because they actually don’t know very
much so what this study is showing is these are young boys with a genetic
disease that’s that’s fatal it’s like multiple sclerosis and and the boys will
be doing karate one month and then the next month they’re unable to walk and
it’s it’s fatal so what this doctor did was they did gene therapy for these boys
and the disease is an abnormal brain immune system so this is brain disease
measured by MRI and then this is one month after they were given the their
own stem cells that had been gene modified and you see all of the grey
dots there’s no evidence of disease in those boys anymore proving beyond a
doubt that in less than a month the entire immune system of the brain can be
replaced so I want to just remind people the levels of fetal DNA that we are
injecting into our children and we know beyond a doubt that these levels can and
do insert into the genome of and they do cause a profound autoimmune
response which triggers labor so the dangers of these contaminants have never
been studied and anyone who says they have and this is an issue that
undoubtedly cries out for a serious scientific study and finally I want to
say that the only thing that we need to do to guarantee that our children will
be the sickest generation to guarantee that we are willing to force mandatory
vaccinations and permanent brain damage on at least one of every 100,000
children the only thing we need to do is continue to be silent and I’ll stop
there thank you

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