what we found is the whole representation of what is happening
is a lie the US government is representing to the public that
this is a health event
but in fact this is a military operation in this episode I sit down
with former pharmaceutical executive sasha latipov
she emerged from retirement during the COVID pandemic to become a whistleblower
after she observed the government and vaccine manufacturers veering away from established
clinical research and public health products
the total volume of adverse events and deaths was higher than all the previous vaccine products
combined we have all kinds of
levels of consumer protections that should be triggered with this picture long before this extent of
injury has occurred yet none of them
bore triggered the government was able to commandeer fromicutical companies to produce these non compliances
injectable products and distribute them this is American Thought Leaders
and I'm Jan call lock sashaladipova such a pleasure to have you on American Thought Leaders
Haiyan think you very much for inviting me well
I've been watching you talk about some very troubling things
over the past months you've become a
I guess I don't know if it's officially about a kind of a whistleblower of course
this is in the realm of
bed genetic vaccine manufacturing what is it that you saw
that made you start wondering that there was some kind of problem happen
I became aware of this
I would say strangeness with the with the whole COVID pandemic response very early on because
am I worked in the firm's cuticles industry
and I had retired before COVID started I sold my companies and I was
enjoying a great life and
spending time with my family and an doing hobbies and traveling
but I when COVID started I was initially concerned like everyone was we didn't know what
it was we didn't know the illness
but I became suspicious Wiener the house authorities started an averted campaign against hydroxychloroquine
which I knew was a safe drug because from the industry I had familiarity with it
I've looked specifically into the issue that they were falsely assigning to it which
is cut prolongation and arythme is associated with drug and us prolongation it happened
to be the area of
focus of company the last company that I had and when worked on farmer
and I knew that what they were saying about this drug was absolutely not true and
more importantly they the regulators knew perfectly well
a that they were saying things that were not true
so that gave me a pause immediately and I started thinking well I mean they're professionals
they know this issue they know this data
yet they're saying things that are not true and that led me to start questioning the
whole thing you know if you catch an official a professional lying about something
in a strait to the public what else are they lying about
and so that kind of started my whole investigation into it
and also I was familiar with the a little bit familiar not
very deeply but I did come across this Marrone class in the
past in my professional work
when these products were in development for other different things very severe
conditions such as cancer for example
and I knew that these products were inherently dangerous witches
not unusual in the Pharmaceutical Research and development we frequently work on things that are
you know they're a risky that can't be toxic such as Kim
agents for example they're toxic
but you know there is application for all sorts of things and you know the risk
benefit profile is always a consideration
and so I knew that these products were inherently dangerous and inherently toxic they
were developed as a cancer
products in the past yet all of a sudden our regulators were all gong he about
oh these are going to be prophylactic vaccines they're going to be
given to children pregnant women
everyone regardless of their health status age
or risk profile vid to COVID so that gave me yet another pause
and I'm so I just became extremely suspicious about this whole situation and that's
how I started looking into it
fascinating well no so tell me a little bit about your background you said you sold
your company so you were but what exactly were you doing and how did you
get into it I well I I'm I'm originally in Ukraine grew
up in the Soviet Union I
worked in mean a while whales was still in new race I
was I worked in a
a industries that contracted for health and IT and I also
did a bunch of international translations of documentation and
in negotiations of companies at a can were coming into the
into the market right after the Soviet Union collapsed so I had some familiarity with the
topic I came to study in
United States from a business degree for graduate degree
and I also went to work for pharmaceutical industry right from the start
I worked in various capacities and eventually started my own
several businesses I call founded and they were all successful and the
last one as I said was
actually focused on card I vascular safety
testing in Pharmaceutical Research and development
looking at electric car Gram's looking at CT prolongation
he noted that the issue that they were assigned into hydroxychloroquine falsely
and soon so that work is its it's con it's called contract
research organization which is a very
broad term their variety of contractors just think if you want to build a very
large and very complicated house how many contractors you're going to hire
well it's kind of like that
so we are involved in a variety of different specialty tasks
and a variety of companies are working toward you know
full feeling these projects clinical trial says but that was my work and then
you know ultimately the companies were successful I sold the last one and I
didn't need to work anymore so I was just you know having a good time
so and you so you were involved deeply in clinical trials
that's what I want to establish yes from many different angles sir
right so the last one was card I vascular safety testing and humans previous
ones dealt with oncology imagine studies arthritis actually worked in all therapeutic areas
my clients were a variety of farmer companies large ones and small ones
Heiser included Heiser was also our research and development partner so we were developing technologies that
they were interested in applying in their clinical trial spaced to make it
know more precise date the collection more accurate more
reliable I'm so partnered with visors several times worked with large one large companies gsk and
artist sisters Annika Johnson Johnson and a variety of small we call them biotechs
so I was very familiar with the space and then what about this manufacturing side of
you know for most of us this is kind of a black box
right you just assume it's done and it's done right exactly
exactly so that's a very big issue but people often don't appreciate
the whole FDA regulation actually it's
it's it hinges on good manufacturing practice regulations so all they're regulate in is
the compliance of the manufacturers
with essentially would manufacture claims about their product
and what they claim on the label needs to be true
and needs to be reproducible in every peel every bottle every girl
everything that the manufacturers ship
so in the United States and worldwide and in special undeveloped countries
we have laws that are similar in the United States it's called good manufacturing
practices it's extensive set of laws
it governs everything the raw materials the impurities the potency the contaminants
you know so it's extremely complicated
structure that every participant of this industry
has to comply with parts of or entirely if you know if you are
selling a drug in the United States
then you're responsible for your own compliance with all of it including all your vendors
you know so it's so comply I had to comply
with part of this as a business owner of a contractor that
was performing work for Pfizer
and we knew how difficult how extensive how tight
everything is regulated that's what people don't really understand its majority of the entire
industry is engaged in some ways in compliance with these rules
and so that's extremely important to know and it's extremely important to follow
you have to prove that the product
has inner certain ingredients in certain quantities and again as I said they are
present in every single dose
of the product so that's why that's why I was always focused on this because I
knew how important it is so you started digging around you noticed that things weren't quite
maybe what they seem so where did you start looking where did you her finding problem
yeah sotofts in addition to you know looking at what was happening with hydroxychloroquine
I became suspicious once the a Marine product
started coming on the market obviously
you know there was a lot of reports of adverse events and deaths which I was
expecting as I said in my I knew this product was inherently dangerous
I and I and I knew that you know there's it's just
going to be a lot of
problems and Doris viewers data based CGC maintains various data based
and there're some others in the UK there's a yellow card and eudravigilance in
Europe and all kinds of other databases they all started showing
huge numbers of adverse events and deaths right away and the government
it was denied that those where associated denying their happening and they
continue denying to this day
so I briefly want to discuss Veras because I had never heard of this
until basically this pandemic and
the way we were taught about verys I mean the general public all right
early on was that this was some kind of poor system that
shouldn't really be trusted because
you know because it's just self reporting I mean roughly that's I remember learning
it about that and then kind of being shocked to learn
that's not how it was considered in the past so maybe just tell me
about that yeah so this is very interesting because when the depending on when
you ask CDC officials about virus
it's either an amazing bulletproof system that is so reliable and they always you
know maintains that's this wonderful data set for them to monitor safety
or it's completely poor and reliable and usually the reports are made up
it just depends on how they want to answer the question right so but historically before
quoted and before it got so contentious
the historically it was considered a fairly reliable database and it's actually
a very important database and while they're saying what it's it's not it's
it's not definitive if report shows up for something that it was caused by this product
but it's a media even on their website that says it's an unimportant early
warning system to identify unusual data patterns
and that's how I was using it I was using it exactly for that purpose
I wanted to look at the data pattern that was coming across
the first immediate finding was that Ted did the volume the total
volume of adverse events and deaths
was you know the tens of tens tents time ten times and
more higher than all the previous
vaccine products combined and the data bus is very old it's I think it
was started in the nineties
and it has reports for about
ninety or so may be close to a hundred different vaccine products
from you know hundreds of manufacturers so you have a very rich data set and you
see the historical ties notes here and then
20 21 comes across and it's this so of course it's a signal
UK it's undeniable there's a signal it's a pattern
you know it needs to be investigated but no investigation ever happened well we
heard we heard that it's they can't find a signal life I've interviewed a
number of people who have spoken directly
I'm with the FDA and it is over the jing miles not seeing any
signal here so that was a that was a signal for me
them the'm not seen the signal because if you have
government officials I'm staring at a very loud signal
and telling you there is no signal that's a signal in itself
and that was a big question to me that was for a
longtime I could not understand
how they were able to do this how they were able to deny the reality
with a straight face and nothing would happen and nobody would be in trouble
or investigated or prosecuted while we have this very loud and clear
signal of huge injuring deaths occurring
to the Americans including pregnant women including children
so that thou was a that was a Big Big problem and big question for me
I couldn't answer it but now I can
and so what did you decide to do so I wanted to
investigate data for myself first
and I wanted to look specifically because they have experience in farmer
manufacturing and good manufacturing practice compliance
I a looked at the data noticed the total number of adverse events and deaths
but also how the pattern of the data across manufacturing lots or batches
so all pharmaceutical products are manufactured in lots of batches
the lots are numbered you can look at dinner if you go to the
pharmacy and buy and ville
you can look on the box it has a lot number so
those are the lot numbers
that can be recorded into the inveyors reports when people submit their reports
and they are not always there because people who submit in their reports which is you
know either patients their relatives pharmacies or doctors
healthcare profession also nurses they don't always have that information so you may not
remember what was what was the badge number you were injected with
you may have you don't have your card with you or the physician doesn't
know so but in about fifty percent
of the reports those numbers are there
and so I was able to match those
lot numbers with CDC Lord numbers I have a list of them
and I was able to see that if the not only the adverse events
were high but the variability of them by batch was extreme absolutely extreme
it was explained that to me with a variability among them set sort the variability meaning
how many are total reports are submitted for particular batch number
so some tech numbers had two or three reports
and some had 5 6000 that should never happen you should never see
if you think about it if you sheobhine
you know Harville today you're experienced if you bind it today and you but in it
a month from now you experience
a month from now shouldn't be thousand percent different because that's really dangerous
even you know if you think a drill a safe medication or aspirin the safe medication
or even if you buy an orange juice and your experience today
and a week from now
thousand times was a thousand percent different
if that's going to be very dangerous you know one of those instances is very dangerous
so when you see a variability like this between batches of what is supposed to be
consistently produced good manufacturing practice compliant product it means the product is not
good manufacturing practice compliant and I as is as comparator because I didn't have
a baseline for this and I didn't have information for example of the batch
sizes at the time I do now and did the story doesn't she
a but at the time I didn't so I thought I should compare it to something
known and something known was flu vaccines
so I extracted all the data for flu vaccines from viewers
and I looked how flu vaccine data looks badge to batch
over a long period of time and by the way it's much more variable
actually a much more a variety of producers making different sizes of batches they're
dozens of manufacturers of lords in's historically and
different sizes of batches and for Florentine it looks as expected
for good manufacturing practice compliant product which a straight line
very close to zero all the batches lineup and there's very little
variability just a tiny bit
and then when you compare them to these corvite shorts
that you can't even put them on the same graph flu vaccine data disappears because the
COVID shorts are variability huge absolutely huge enormous
so I knew at that time which was toward in middle
20 21 tour the George for of 20 21
I knew for sure they were not good manufacturing practice compliant
so we have not good manufacturing practice compliance product being produced
shipped in millions of doses and injected in millions of people including pregnant women and children
we have a CDC and FDA lying and saying there is no signal at all
and this continues for a longtime and then eventually if you know I
ran across a research by my now collaborator Catherine Watt
she's done a incredible legal analysis of
how the government and the healthcare agencies are what set of laws
they're utilizing to enable this
to enable to subvert the good manufacturing practice
compliance laws and be able to continue denying that there is any
any injury or any das or any problem occurring with this
with these products for a longtime and this dis continues to date
what we found is the whole representation of what is happening
is a lie it's basically the US government is representing to the public
that this is a health event and a response to a health event but in fact
what they are doing is a this is a this is a military operation
these so called vaccines tereli vaccines
but these injections Hare being manufactured under defense contracts
utilizing a Defense Production Act other transaction authority
and emergency us Essary station under public health emergency so when these things
are used together then good manufacturing practices do not apply
to these products at all even legally even legally so there's this law
on the book the 21 sec 3 60 BBB
that says if emergency use authorized counter measures
under public health emergency cannot constitute Clinical Investigation
so Clinical Investigation is actually not possible for these counter measures
and if Clinical Investigation is not possible then you cannot have clinical trials
you cannot have informed consent you cannot have clinical trial subjects a clinical trial investigators
so the utilizing the structure of emergency is Essary station public health emergency the
transaction authority Defense Production Act
the government was able to a
commandeer pharmaceutical companies to produce these non compliant injectable products
and distribute them calling them a medicine where in fact it's not a medicine
it's an act of war
they're used in Defense Production Act in machinery
United States Military even internationally this is been distributed from this military to overseas militaries
a not pharmaceutical distribution chain so they're using the military machinery to distribute this noncompliance
products including biological chemicals
Allard kinds of ingredients we don't really understand very well
am and call it public health and medicine
first of all this sounds so fantastical
what you just said right what really
that's crazy now one thing I know for sure is not crazy which is the
the fact that it's the military that did the distribution that's official that's actually by
that's public knowledge that was announced I know people who are responsible for the
distribution and they're very proud of
doing the distribution because you know they felt it was the only I guess
structure in society that's able to
ploy something like this fast enough right the that I have that on record now
but what about this other of these other parts like that this is this is actually
the US government contracting
these pharma companies to develop a character measure against
what well the countermeasure is a very important legal term so and I advise
people to look it up
so a countermeasure it's a very fuzzy term first of all so anything can
be a countermeasure a lock on the door is a countermeasure against a breaking
I and so call it something a countermeasure you're already rare move
as precision of the legal definitions of a pharmaceutical for example so but we
know already it's not a pharmaceutical
I'm and also you know what I'm saying not
it's not a conspiracy definitely not because the law that I just described is
21 sec the sixty BBB it's cited by everyone including the FDA in their documents including
by the manufacturers in their documents
False Claims Act case was dismissed I'm the judge you can read the dismissal
of this case the judge agrees with what I just said
the he agreed with the fact that wiser wasn't supposed to be compliant with good manufacturing
practices per contract with the department of defense
that they were producing counter measures that they were producing large scale manufacturing demonstration which is
how these things were ordered from the government
he essentially describes this in a more sophisticated hundred page document based on a contract based
on a contract right that Pfizer produced
revised produced their DOD contract and since then
hundreds of department of defense
contracts for quo vet counter measures were released through one although they're partially redacted
but I read a lot of them and they're all on line am I've read the
Fisher moderna once and some other vaccines a
and they're all essentially similar they're utilizing the structure
of ordering counter measures
ordering prototypes department of defense ordering it
from the pharmaceutical manufactures under Defense Production Act under other transaction authority
and the good manufacturing practices are not part of it at all
so this product by statute and by contract with department of defense
it does not need to be compliant with good manufacturing practices
and then another additional part of this whole scheme is this Public House emergency announcement
so when Public Health's emergency happens
essentially the executive branch of the government usurps the power from legislative and judicial
a Public Health's emergency by various illegal amendments and acts over a long period
of time has been created into this
a have to say trigger that triggers this whole system
where the HHS secretary becomes like a de facto dictator
so has secretary is the sole person
and who can deploy these products in the United States so if the need not
be part of it in the law it says that has secretary he or she whoever
that happens to be used to used to be Alex Azar who was under
Trump and now it's had a Besser
they can determine whether these counter measures can be deployed in the United States
based on available data if available
does not have to be available and based on his own
determination about current risk benefit profile and future risk benefit profile
and again he can take advice of whoever he wants to take advice
but the decision is up to him and so that so that's very interesting because it's
also counter intuitive your it's a DOD operation why is the HHS secretary
responsible for the deployment in the structure of public health emergency it's a militarized structure so
they emerge in it's all executive branch so
hcs and DOD become kind of one organization and they also
rap FDA in terms of this operation in terms of separation I also
the public health emergency becomes that trigger for essentially invoking all these military type of laws
saying that do know now that now there now there we know one organization
oh there's also interagency agreements that going to this where they determine confidentiality determine
how they're going to make these counter measures and so forth
but the so the HHS secretary deploys them quite orders them
a they get funding a
and than FDA kind of rubber stamps everything and pretends that they're regulating these
things but they're not they're
impersonating regulators basically because there's nothing in the law that says that
FDA regulates countermeasures they don't
a but you would think someone would want to know
let's say I've had a number of people on this show who have been pretty serious
vaccine injuries for example in one of the sort of pieces of fallout from
this scheme that you're describing is that
you know these the idea that these people could be harmed is
kind of denied by society
certainly denied by the authorities not a hundred percent there's admissions in the NIH
and solver that's rare right
but mostly they say there's no signal mostly they say that this doesn't work
people are diagnosed with anxiety and
things like that haha and it seems this seems to be linked
to this idea that this is somehow not a health response I don't know
what your thoughts are on
I understand why the government denies it clearly
I still can't wrap my head around denial of you know of this happening
by regular let's say regular physicians
I know that there's a monetary structure that incentivizes this behavior so there's definitely am
payments from Medicare Medicaid for to the doctors to vaccinate
bonuses for numbers of vaccinated vaccinations they administered bonuses especially very high bonuses
to vaccinate somebody who hasn't been vaccinated so there's high price
only on the heads of people who haven't been vaccinated
to too get the injections in and to give boosters and so forth so
there's huge monetary incentive there
also the entire structure is
essentially the government extended its sovereign liability protection to everyone who complies with this system
so throughout this whole structure of
of producing these injections distributing them injecting them than denying the injury there's
huge not only made monetary compensation and incentive but also liability protection
through prep act and that's explicit also in the DOD contracts with vaccine manufactures
and not just vaccines actually I it's
goes with entire quovit counter measures
Production Act which includes vaccines therapeutics monoclonal antibodies blood products diagnostics
even masks and swabs and staffing and things of that nature
all of them have this clause that says prep a
a liability exemption clause which describes that if you were in compliance with all
of this then you were treated as a covered person under this act
and you are exempt from liability if you essentially followed the orders
and the last sentence of that clause says that this is both civil and military application
this product is both civil and military application and by the way the contracts are redacted
with most common reductions there are two reductions
by six and b four b six it has to do with if we reveal this
information it hurts US foreign policy or US
foreign relations and if before it's if we reveal this information we reveal an
information about state of the art
technology in the US weapon system he
like somebody to answer this I'm just listing set of fact
you can make your own conclusions but I'd like somebody
am Nino answered this question why and what
is being put in these injections what are people being injected with
because we know there's huge amounts of deaths and injuries
but we can't address those injuries until we know what they were injected with
we still don't know that an I mean ostensibly it's a
you know MRNA synthetic Marina in a lip id NATO particle envelope
does not you know that activate
a production of synthetic spike in the body to create an immune response
I mean that it definitely does that but there's more to it I guess that's what
you're saying right so that's what's claimed I know you just said is claimed
on the label of the product
but I have described before when off ashore their not good manufacturing practice compliance
which means they can't themselves
verified to themselves that's what they're making right so
so we they're probably making that in some instances but there's also
a whole bunch of other
effects and varieties and by the way if the product does not good manufacture
in practice compliant it's open to adulteration and falsification whether on purpose or accidental
so we have now the whole bunch of unknowns happening
right you know I remember this scene where doctor Renata moon you know opened up the
mar I forget which one but was one of the mRNA vaccines
co insert you know as
Bobby Kennedy Jr says the one place where the vaccine companies tell the truth right and
she opens it up and all that's on there it's intentionally left blank or something close
to that I unsealed the box with the
and try using Canon and then I pulled this out and this
is what it looks like
Fred like to hear he bore it is sorry about that
it's unit's blank bond lights
and there it is this does intentional Ebling
that's the data that pharmacist en physicians are basing on giving the injections
outside of mainstream media recommendations there it is right there
here's a good question why didn't they just print that on a piece of
paper the size of a postage stamp
why all the theatre of folding it up into a Great Big
piece of paper like that why
tat've had osioutsitsand that's what's passing for informed consent
right so how am I to get in for him to consent
to parents when I have
this is what I have I have a government that's telling me that I
have to say safe and effective
and if I don't my license is a threat am how am I to
give informed consent to patients
we're seeing an uptick in myocarditis we're seeing an uptick and adverse reactions
we have trusted these regulatory agencies I have
for my entire career up until now
something is extremely wrong to your point
you also have talked about the variation between the batches
you know in some interpretations might almost look deliberate and I found
that it would be very strange
yes this was one of the findings a
pretty early on I when the nws said I was looking adverse data and looking at
the variability of adverse events and death
per batch number so in addition to seeing forcible huge
adverse events and death rates overall we saw huge variability batch to batch
but that variability was also not random meaning that it's not just that they're not
they don't control their process and they're producing random outputs
there's some sort of a design going on as far as what's
in those vials and different batches
a they depending on the letters used in the in the alphern Merrick number and which
should be just random and should be just I know some sort of a
manufacturing scheme to keep track of things
but depending on the letters we knew that this set of letters would produce higher toxicity
and this set of letters would produce lower toxicity that should never happen
we also had cluster ins by dates of manufacture also should not happen you should not
have a difference between he product produced
on the first of the months or in the thirties of the
months you know making an example
I another'm a colleague of mine from Denmark was able to obtain
this was recently published in a peer review journal of European clinical investigations
he published this data so he obtained data from the Danish government
Denmark was a visor exclusive
they got all the badge numbers for Pfizer and the adverse event
data and he was able to find
three different patterns of toxicity and they're cleanly separated from each other again
we have variability of toxicity but it's also alliance in three patterns
and there's nothing in between meaning that this is not actually random it's by design by
design they have three different levels high medium and low and the Force One
meaning something as apparent as plausible
because those people who were injected and don't submit any reports they
don't have any adverse events
so we have at least four different levels of toxicity
detected in the data from adverse events
and again this should not happen this should be explained there should be investigation
and by the way you know everything I'm saying you know once you see some variability
of data like this is huge variability the clusterings of data in various
but by various parameters there are numerous different safety produce that should be triggered
at the manufacturers themselves should detect it
manufacturers should recall these products you know should stop the production lines
and start investigations that's what
they do normally the government you know if the manufacturer is not doing anything about it
then FDA has all sorts of enforcement powers
they can also force recall force investigations
you know we have all kinds of levels of protections consume protections that should be triggered
with this picture long before you know
the this its extent of injury has occurred
yet none of them were triggered none of them were
so all of them fell apart simultaneously and that's you know kind of
kills me ii I feel like I've been screaming for the last
two years in the empty space and inner nobody's paying attention to
this have you experienced any blowback
I tried to post this on a more mainstream social media is was immediately
banned and cancelled everywhere
I still can't get my Twitter account back I me I can use it
on laptop but I Can't Have it
my phone Instagram deleted my
art web signed it was counter percent dedicated to art you know it had
nothing to do with this
yet they've bound it and they can never get in ste Gran back a so yeah
but other than social media censorship not really you've been in the middle of this industry
by a pro pharmaceutical industrial complex has some people right
you're aware of its size and power so
did you think it all twice about disclosing these things as you
started you got curious but
I don't worry about it yes I know they're powerfully they can you know if they
wanted to kill me they'll kill me but that doesn't concern me because
I think that they the evil that's unfolded in the last
two and a half three years is unfathomable
to most people and most people prefer to deny it
than to deal with it and I don't deny it Andy and I don't want I
want people to have the knowledge that I do from my professional background and I want
them to understand what's going on
so that people can stop and in fact we have been successful so far because the
uptake of these shots now is at zero it's practically zero there's huge distrust
in the pharmaceutical industry in the health authorities people are questioning it
by spill over the questioning childhood vaccinations schedule which I think is a great
development they should question it
because people who are able to do this with these shorts
well where else are they lying what else is going on
you have to question all of this and so appropriately people are becoming very skeptical
very concerned protective of their children and I think it's a great development as far as
justice and investigations and reform that should come
I hope it will but that's just going to take a longtime but at the moment
I think everyone should understand what happened
understand the truth and stop taking these injections
do you have a theory about what happened that's been all pretty
speculative to answer this question
too many people who asking me why and I say this I can't get
in the heads of the criminals
MI can just tell you that this is what they're doing you know I
have to backup to everything that I just said in terms of fact
in terms of the laws that are being utilized in terms of the unknown
compliance that's evident the injury that dos
they all ties together I can show you how they preplen this
why they're doing it we have to ask them we have to
put them on the stand
and explained themselves well you know one of the things I've been
hearing a lot about is
at the very least a lot of accelerated research for example in applying this mRNA
a vaccine technology to livestock for example and people are concerned that this will
be something that'll enter the food supply what are the ramifications we don't know
hearing everything you just said right
it sort of adds an extra serious twist right if this is if all this was
created without the proper regulatory oversight going far beyond the basic concept of EUA
basically that's what you're contending
why is it that this has now triggered accelerated
research into the deployment of such
home products for livestock that's a great question and its note resources just deployment
so because you know have you seen that's the speed with which they just
set off and now we're going to put an into the food supply or
you know recently the bivalent boosters for example were approved based on eight mice ran
I mean the insanity of what I just said you don't need to any
other conspiracies here is to come
thru to just understand this you know if I told you five years ago
that there's going to be an injected product forced on every man woman and
child in the United States which was approved based on eight mile data
would you think that I'm not that well yes and I would think that
I'm not at that time but this is the reality this is would happen
and ten they just by Dick that
they decided to oh now we're going to inject old cattle with this stuff
there was no studies nothing was tested you know they tested it on mice but they're
going to put it in cows
I don't actually know this state of deployment but maybe you can explain well
there they're basically going putting a bunch of money in front of
they know cattleman associations agricultural associations
and they're saying well now we're going to convert all the either convert the previous cattle
vaccines or just done new marinade shots
for cattle for what reason what is the what is the emergency with cattle
is there pandemic of cows of some sort that we haven't heard of
you know why all of a sudden they need to be injected with a Marine
and somebody needs to answer that I don't know the answer to this so lines this
has begun or yes the deer
there a there have been news reports that
at least some of the in said that there were going to be some
associations that are going to be forcing inner cattlemen associations a going to be
forcing this into the onto the
participant of their membership and that this is going to be regulated
that the cattle vaccines are supposed to be now marinade for some reason
and also they're going to convert traditional vaccines for humans traditional
childhood vaccines and vaccines for other like flu and
some other indications also convert them into market and that's published
in preview journals al these plans that you know
we we're working on all these COVID vaccines you know next we're converting all
these vaccines into mRNA platforms
is it just a mania is it is it a mania about this
that everyone eats of they were so safe and effective you know they was this huge
a information blitz right oh safe and effective you're going to kill grandma if
you don't take it they're many
pieces of messaging billions of dollars spent on her
and so you know my question in my mind right is just simply are
just some people of some people have just become kind of
obsessed with at its technology because it's so great we've been told it was so great
Patricia yet's a great moneymaker for
certain people obviously that there's a lot of money has been thrown
at it by the government
and would the government also come the private investors because they convert frequently you
know various types of investors
including private and in of public funds and so forth
they see this spigot of money that opened in this direction and
of course they all follow
because CEOs such a great that's just how it works yan read bonanza
am and that's so that of course creates a lot of
financial momentum behind this but scientifically and
you know technically their claiming it's so it's much easier to make these vaccines because it's
by chemical reaction is the don't have to grow any cultures and so forth
so their claiming it's also technically
easier to manufacture what I have not seen is any benefit of
it I only see injury
well I mean because these are by all accounts actually failed products
isn't so it's surprising that
this technology would be deployed broadly in many areas or the inter even the
interest for it to be deployed broadly
yet they're not only failed they're also dual use
technology has only been designated dual use meaning military and civil justice
they're stating in the prapapact clause
it's been designated Doles technology since at least the nineties its current use indistinguishable from its
weaponized use because you can't really
as a consumer or even as a manufacturer it's very hard to
ensure that code that you're cod in is actually the correct Cote
the Marine code in the vial oh I see I see it's very easy
to subvert it to change it
to introduce other codes
am and a to introduce other
or say nefarious types of pieces of cold into it
and if you don't know what was introduced you don't have an
assay to test for it
so it's completely open to adulteration and falsification and is it correct they have
never either the technology has been in development since the nineties
a but no products have come to the market out of it no successful
medical products because of all these
problems I've described the manufacture ability of it as is you you can't really make it
consistently a good manufacturing practice compliance
and it's wide open for these falsifications and weaponization type of approach and it's
also documented and a lot of
literature including NIH textbooks military reports
on bioweapons technology has very well documented this phenomenon and so the use of it
is indistinguishable between me supposedly medicinal use that has never been demonstrated
and weaponized use that has been demonstrated and so that is that whole
you know obsession with this technology seems extremely as I problematic to me like very questionable
somebody again has to explain how do you
distinguish between weaponization use of this technology
and what you claim is you know beneficial medicinal use
yeah that's a great question so I just want to clarify when you're talking
about the God You're taught yours basically saying that the mRNA that goes into
that technology than is then delivered
by the way that the mRNA vaccines ware delivered that code is subject to change and
you can introduce some other Marina
and you wouldn't even know to test for it if you didn't
know what was put in there
weekend since the whole system is a black box
it's very hard to actually track and for it yeah for it verified
and in fact it's been allowed by the regulators so another thing
I haven't discussed yet but
at the end of I think you've also covered an your publication at the end of
20 20 there was a leak from European Medicines Agency
and a bunch of documents were released Pfizer manufacturing documents at the time of the approval
and the a bunch of emails between Ma staffers that were discussing this
and in these documents it was clear that at the end of 20 20
they European medicine's agency deemed a visor not good manufacturing practice compliant
it was number one objection from the regulators to their approval
and too they found this issue of marinade breaking down
and creating a broken pieces of a Marine broken co ad
and at the time de Fisher told them that the standard for
for approval should be fifty percent of marinade should be consistent with the declared code
and the regulators went alone with it so because the product was approved in Europe within
weeks of this discussion that was released
so fifty percent of marinade should be consistent
with the code that they declare for b and T1 6 2 2
and then the other fifty percent is unknown
right they lowered the standard they lowered the standard arbitrarily for themselves and regulators
somehow miraculously agreed with that nonsense
but which means that fifty percent is undeclared
fifty percent can't be practically any sequence it could be any designer sequence you can make
and if you made the designer sequence and didn't tell anybody what it is well how
are you going to make assay
to test for it you can't right it just looks like another band and
Titus looks like another band that just looks like a piece of marinade we
don't know what it colds for
but you can introduce all sorts of different things into it
and that's how you weaponized and actually that's a that's described as a weaponization
technique for ginserapies is a weapon
by in the book that was published is a whole chapter on this
there's a text book on line is published in 2000 and 18
that's exactly how it's described and that's exactly what they put into the approval
and that's what went on the market please let's discuss this openly
somebody has to explain to us how are they determining that these vials
are not the weaponized use of it but a medicinal use
any final thoughts as we finish I mean thank you for
thank you for inviting me in the great conversation
I my wish for this for this information is to be discussed shared
you know challenge it please prove me wrong
you know look at these documents prove me wrong but more importantly
I'd like some investigations to start
open investigations public investigations how you know answer how can we answer these questions
because this information will help
people who are vaccine injured because if we answer these questions we
know what they were injured by
well sashaladipova it's such a pleasure to have you on the show
thank you very much thank you thank you all for joining sasha Zaripova and me on
this episode of American Thought Leaders I am your host Jan call lock