https://haunebu7.wordpress.com/2020/09/08/biologe-enthullt-massive-gefahren-der-corona-impfung-und-der-zulassung-nach-bill-gates-c-arvay/
Main statements by Clemens Arvay:
-- Clemens Arvay is a microbiologist in the field of plant
virology for additives to vaccinations, so he is very
familiar with vaccinations
-- Bill Gates said: Vaccines take at least 5 years to
develop with enough testing and waiting for long-term side
effects
-- Bill Gates then said that the test phases for Corona19
vaccinations should be "nested" (criminal
telescoping)
and run simultaneously without waiting for the long-term
side effects
-- the vaccine from AstraZeneca which is bred on monkey
kidneys had it's first test phase with 544 healthy subjects,
but in 47% there could be watched a reduction in white blood
cells, which provokes a susceptibility to infection (
neutropenia,
reduction in neutrophil blood cells), which is normally a
maximum of 1 to 9% only ("single digit range")
-- So it is absolutely incomprehensible why the health
ministers of Austria (Anschober) and Germany (Spahn) have
already pre-ordered millions of vaccine doses from
AstraZeneca WITHOUT knowing exactly the side effects
-- there are still two mRNA vaccines in preparation, a
completely new process [the criminal vaccines of
Pfizer/BionTech and Moderna, then also Johnson&Johnson]
-- there are already mRNA drugs against cancer where severe
side effects are accepted because cancer is considered
"incurable". However, Corona19 can now be cured, and that is
why one should by no means accept such severe side effects!
Biologist Clemens Arvey warns of the long-term side
effects of the AstraZeneca monkey vaccination [1]
The transcript (translation):
1. Introduction:
The video in honor of Dr. Bonelli and RPP Institute
This video is about the risks of the Covid19 vaccines
(5''), which are in the pipeline for being approved in a
fast-track process (8''), and which we are now facing
(10''). Austria has already ordered in advance, as has
Germany, millions of times (14''), and some of them are
already being produced (17''). What risks are involved and
what dangers, that's what this video is about right now,
which I have made exclusively for Dr. Raphael Bonelli do
(26''), and for the PPR Institute (30''), as thanks and
recognition for the courage that Dr. Bonelli and his team
have been on the scene since the beginning of the Corona
crisis (37''). Because I know from my own experience how
difficult it is to represent dissenting opinions (44''),
to advocate a course that also includes criticism of the
government (49''), and I know how much hostility it causes
and one has to bear (54'').
2. Field of work:
Biologist Clemens Arvay
I am a biologist myself. My focus is health ecology
(59''), but I have also dealt with controversial
biotechnologies for years in previous books (1'6''). One
of the universities at which I studied is also very much
involved in the field of biotechnology (1'15''). This is
the University of Natural Resources and Life Sciences in
Vienna (Universität für Bodenkultur in Wien) (1'18'').
Yes, it's not just about agriculture at this university,
it's also one of the largest biotechnology centers,
academic biotechnology centers in Europe (1'28''). And I
studied ecology, first in Graz, and then plant science
(1'33''), and applied plant science, which also has to do
with biotechnology (1'38''). Few people know, but plant
scientists also work in vaccine research (1'44''). For
example, they are investigating the use of plant viruses -
there is also a plant virology in the area of vaccines
(1'53 "), and [there is] also the use of plant adjuvants
[ingredients] in vaccines (1'57") ), there is a medical
botany etc. etc. (1'59''). And that's how I got into this
area of biotechnology - except for health ecology
(2'6'').
I would like to add right away that vaccines are good and
important drugs (2'13''), but only if they have been
tested for a long time and in accordance with the
standards (2'18''). Only then vaccinations are safe and
can also be recommended as useful drugs (2'26'').
Unfortunately, this is not the case with the vaccinations,
which are likely to come to us soon because of SARS-Cov-II
(2'34'').
I wrote an article for the Swiss Medical Journal
(Schweizerische Ärztezeitung) (2'39'').
Article:
Genetic Vaccines Against COVID-19: Hope Or Risk?
(orig. German: Genetische
Impfstoffe gegen COVID-19: Hoffnung oder Risiko?)
You can read it
through if you want (2'41''), it's about the basics of
genetic vaccines (2'46''). How do they work? (2'48'')
3. The criminal genetic vaccines:
The theory: how do genetic vaccines work? -
manipulation of protein biosynthesis
Now in a nutshell: How do genetic vaccines work? (2'51'')
Genetic vaccines no longer bring a virus into our body,
neither weakened nor dead nor alive (2'58''), not even the
protein of a virus (3'0''). Instead, they bring in parts
of the genetic information of the virus, e.g. the
coronavirus (3'6'').
And this is how genetic processes in our cells are
manipulated (3'12''), not in the cell nucleus, but OUTSIDE
the cell nucleus (3'15''), as part of the so-called
protein biosynthesis (3'19''). This is a process in which
our body continuously produces proteins every day that we
need to function, that means: so that our organism can
function and to stay healthy (3'33'').
Theory: Genetic virus material changes the biosynthesis
of proteins: Production of a viral protein, the "viral
antigen" - the immune system fights against this "viral
antigen" with antibodies / T cells - RNA + DNA vaccines
And then - this genetic substance - this genetic material
from the vaccine - intervenes and causes our body to
produce a viral protein itself within the framework of
protein biosynthesis (3'49''), and that is then the viral
antigen (3'51'') to which our immune system should react
(3'54'') and should form antibodies respectively the
T-cell immunity (3'57'').
Yes? So you no longer bring in the virus, but the genetic
information of the virus (4'2''), and the viral antigen,
which is brought in normally with a normal vaccine
DIRECTLY, is created now IN OUR BODY (4'10''). So we are
used as copy machines for viral proteins (4'15'').
In this way mainly work all the RNA vaccines and
the DNA vaccines (4'19''). As I said, you can
study this article, which I wrote for the Doctor's
Newspaper (Ärztezeitung), more closely (4'25'').
The THIRD variant: Viral vector vaccine
And then there is a third variant (4'28''), an extended
form of genetic vaccines that works on the same principle
(4'33''). However, the genetic material - the genetic
information of the coronavirus there - is introduced with
a "vector virus" - a carrier virus (4'42''). And those are
the viral vectors (4'44'').
And this genetically manipulated virus is then inoculated
into the body (4'51''), and integration mechanisms are
working provoking that the viral antigen is created in our
body (4'59'') - this is just an expanded form of genetic
vaccines (5'4'').
In principle, all genetic vaccines intervene in these
genetic processes outside of the cell nucleus (5'11''), so
that something is created IN US: an antigen (5'14'').
And it's in this way one has to imagine how are these
genetic vaccinations (5'19'').
[There is the warning of Dr. Tenpenny and Dr.
Cahill and others: The mistake of these vaccines is that
one cannot stop this antibody production and the immune
system becomes too strong destroying the own body at the
end when a new virus comes - the Challenge Test in 6
months is deadly. The trial animals all died after 6
months].
4. The highly criminal gene vaccination
from AstraZeneca WITHOUT long-term studies:
The gene vaccination favorite: The monkey vaccination
of the eugenics royals from AstraZeneca from Oxford
The big favorite comes from Oxford and is such a viral
vector vaccine (5'25''). But there are relatively far
advanced RNA vaccines that are also considered favorites
(5'31''). And there are even some DNA vaccines - [they
are] particularly problematic, because under certain
circumstances it could very well lead to an unintentional
incision in the cell nucleus (5'42''). But that's another
chapter. This may be discussed well another time (5'47'').
Fortunately, this DNA vaccine is relatively not so
developed yet (5'52''). And right at the front is this
Oxford vaccine, right at the front (5'56''). World Health
Organization ([Pharma] WHO) lists this vaccine from Oxford
- this viral vector vaccine at the top (6'4''). It is the
most advanced in clinical testing (6'6''), it is the most
pre-ordered internationally (6'10''), more than TWO
BILLION cans have already been pre-ordered worldwide
(6'14''). It is already in production (6'17''). It is all
over the media. Bill Gates invested in this vaccine right
from the start (6'22 "), so [he] [pushed] this company,
[he] is an investor in this company (6'25").
And Mr. Karl Lauterbach, the German SPD health politician,
has already congratulated the vaccine on Twitter (6'33'')
and assumes that the chance is very high that we will have
it soon (6'36''). The newspapers [censored by the Mossad]
are full of the vaccine (6'38''). I say this so clearly
because I am told again and again that I'm talking about
vaccines that don't exist (6'42''). Of course there are
vaccines (6'43''), they are already being tested (6'45'').
If there isn't a vaccine, I can't test it (6'48'').
The approval of the criminal, genetic vaccines will be
in a short time - manipulations in the Mossad media
without end!
And yes, of course we can assume that these vaccines will
be approved (6'53'') because they are racing towards
approval (6'56''). I'll come back to that in a moment
(6'57''). They are hiped [advertised]. They are produced
millions of times (7'1''). They are already pre-ordered
(7'3''). They will be announced to us for spring at the
latest, maybe for autumn (7'7''). So no, I'm not sucking
it out of my fingers (7'10'') that we can count on the
vaccine from Oxford, for example (7'13''). Unless the
resistance is too great, yes? (7'16'') - That is of course
a different situation not toughing it finally (7'21'').
But at the moment it seems not like this (7'23'').
Criminal monkey vaccine from AstraZeneca: Vaxitech
company has the patent - based on a GENETICALLY MODIFIED
chimpanzee virus - AstraZeneca does the marketing
There is one more point, before I go into the vaccine and
the risks in more detail (7'29''), concerning the big
European favorite from Oxford (7'33''), I would like to
say that it is originally from the Vaxitech company
(7'37''). So: This company Vaxitech has the patent on this
vaccine (7'41''), which is based on a chimpanzee virus
(7'44'') that has been genetically modified (7'46''). And
the company Vaxitech is a spin-off company from the
University of Oxford (7'52'') - was thus founded by an
employee of the university - Sarah Gilbert - (7'57'').
That means, it is wrong to say that it is a vaccine from
the university (8'1''). But this is the vaccine of a
spin-off company (8'4'').
This vaccine is produced and marketed together with
AstraZeneca (8'12''). AstraZeneca is a large
pharmaceutical company that is cooperating with Vaxitech
here (8'20''). So if you hear about this vaccine it's
either called the "Oxford Vaccine", or the "AstraZeneca"
vaccine (8'27''), and then you know that it's about this
vaccine I am speaking about (8'34'').
5. The manipulated approval phases: Bill
Gates' ordering the criminal "telescoping":
AstraZeneca Monkey Vaccine Tests:
Test Phases Are "Pushed Together"
So: The vaccine was already tested in the first and second
clinical phase (8'42''), and the first and second clinical
phase were pushed together (8'47''). This is something ...
em ... ALL phases are pushed together, not only with this
candidate, but also with all the others (8'53'').
The manipulation of Bill Gates: Approval phases are
pushed together as "telescoping" - minimum until today:
5 years development time
This is something that Bill Gates proposed publicly in
April [2020], and probably planned long before that
(9'0'').
Article:
What you need to know about the COVID-19 vaccine
He suggested that the
admission phases be SLIPPED into one another (9'5''). This
is called "telescoping" (9'7''). And he himself said at
the time: The fastest vaccine that was ever approved was
one that took 5 years (9'17''). So: The world record for
the approval process, the safety process for the vaccine
was FIVE years (9'25''). No vaccine has made it faster
(9'27''). The average is 8 to 12 years (9'30''). And that
should now be compressed to months (9'34''). And then Bill
Gates suggested this pushing together, this telescoping,
which is now happening everywhere (9'42'').
Article:
How soon will a vaccine be ready?
[Bill Gates bought
the pharma so they do what they want].
Criminal "telescoping": No more waiting for the
long-term consequences - no more care - investigation
phases are carried out in parallel instead of step by
step
That means: things, steps that should actually be based
one after the other step by step (9'49''), now happen in
parallel to each other (9'53''). And waiting times, which
are usually observed, which are also important in order to
absorb long-term effects, delayed effects, are no longer
observed (10'7''). That means: This is of course a shorter
time of process, and one could say: Formally, every work
step is done (10'14''). Yes, but not with the usual care
(10'16''). [They're doing that] parallel to each other.
One does not wait for the evaluation of one of them before
the next [step of the test] begins (10'22'').
And so it came about that the first and second clinical
phase - there is always a preclinical phase first
(10'27''), first in the laboratory with cell culture and
then in animal experiments (10'31'') - and then will come
three clinical phases (10'34''), and the first and second
clinical phases for many of these vaccines - also in
Oxford - were SHIFTED TOGETHER (10'40''). So they
fulfilled the tasks of both phases in the same time - done
in a very short time (10'46'').
Criminal "telescoping": The evaluation of the
preclinical phase with animal experiments is NOT
awaited!
And there is something very interesting: When the vaccine
from Oxford by Vaxitech - this viral vector vaccine
(10'55'') - was administered to humans, in the first and
second - that is, clinical phase pushed together (11'2''),
there were still no results presented of the preclinical
phase (11'5''), namely no evaluation of the primate
experiments (11'10''). The vaccine was tested on rhesus
monkeys (11'13''). Well, these primates [monkeys, higher
mammals] showed antibodies being formed that were also
detectable in the blood laboratory (11'21''), but: As a
result, when these monkeys were exposed to the virus under
natural conditions, they were NOT sufficiently protected
by these antibodies [they did not pass the Challenge
Test!] (11'34''). They were infected just like the
unvaccinated (11'37''). So the vaccinated monkeys got
infected EXACTLY like the non-vaccinated ones (11'42'').
Article: Doubts over Oxford vaccine as it fails
to stop coronavirus in animal trials
6. No vaccination protection available!
AstraZeneca animal experiment: The gene vaccination
does NOT protect against new infections!
They were only protected from severe lung damage
(11'45''), but not from infection, and in the nasal
secretion of the vaccinated monkeys as many viruses were
found as in the nasal secretion of the non-vaccinated
monkeys (11'54''). That means: They were just as
CONTAGIOUS (11'57'').
That is very important to emphasize (12'0''). A
vaccination must also ensure that these people are not
contagious (12'5''), and a vaccination that averts only
the most severe damage and otherwise still leads to an
infection or cannot prevent an infection (12'16 ' '), does
not have a particularly good impact profile (12'19' ').
This has to be stated very clearly (12'21''). [This
vaccine is TRASH - nothing else].
One of the most important contemporary geneticists -
William Haseltine - has ALSO documented this and commented
this (12'31'').
Article
by William A. Haseltine: Did The Oxford Covid Vaccine
Work in Monkeys? Not really
And he also says very
clearly: The result shows that the monkeys were NOT
protected by the vaccination (12'36''), that they were
infected DESPITE the vaccination (12'39''). Ok? If just as
many viruses are present in this nasal secretion, then it
is just an infection as in the non-vaccinated (12'47'').
7. AstraZeneca monkey vaccination: Far too
many side effects + neutropenia in 46% of the
vaccinated:
Criminal "telescoping": clinical phase 1 with students
far too early + far too many side effects
And despite of all this, there were experiments with human
object already in this time (12'55''). Well. What was
shown with this? (12'59'') It was shown that in the
clinical test with humans - with human objects, these were
over 500, about 544, they got the vaccine injected
(13'11'') - and there was a noticeable cluster of
vaccination side effects (13'16''), namely
-- up to 70% - this means: 70% of the test persons
complained of symptoms of illness (13'23'') such as the
fatigue syndrome [eternal fatigue] (13'25'') after the
vaccination,
-- 60% about flu-like symptoms (13'29''). This also
includes a slight fever or an excessive temperature with
headache, pain in the limbs, chills and so on (13'38''),
temperatures up to 38 degrees (13'40'').
-- And still 18% complained about temperatures with OVER
38 degrees that occurred (13'47''). Ok? And
-- also systemic muscle pain occurred, this means: muscle
pain that can occur all over the body and not only at the
location of the vaccination's injection (13'55'').
And that happened with an accumulation that was
significant. The authors of this study, who are themselves
economically interested in this vaccine, were also stating
this (14'7'').
Article: Safety and immunogenicity of the
ChAdOx1 nCoV-19 vaccine against SARS-CoV-2: a preliminary
report of a phase 1/2, single-blind, randomized controlled
trial
The comparison group with a
meningococcal vaccine - the AstraZeneca vaccine is
WASTE
A comparison group was made with a meningococcal vaccine
(14'11''). And although the meningococcal vaccine itself
has a relatively bad side effect profile (14'18'') -
that is, it produces a lot of side effects compared to
other vaccines (14'21'') - compared with the Covid19
vaccine, this Covid19 vaccine was still there always
worse than this meningococcal vaccine (14'29'').
The P value: 0.05
The P value given by the authors for this accumulation
of side effects is less than 0.05 (14'37''). This means
that the probability - that these frequent side effects
were a coincidence product - is less than 5% (14'46'').
The result is therefore significant (14'48''), which is
not surprising even with this large accumulation of
symptoms of the disease, up to 70% (14'53'').
Something else is added, and that is MUCH MORE RELEVANT
(14'57''). That can no longer be trivialized (15'0''):
The sample: Neutropenia (reduction in white
neutrophil blood cells): causes susceptibility to
infections!
There was also a random test: every tenth person was
subjected to longer blood monitoring (15'6''). This is
actually a task from the first clinical phase that was
simply integrated into the second [clinical phase]
(15'12'') - ok? - because of the telescoping (15'13''),
because of the pushing together (15'15'').
And it showed that 46% of the vaccinated developed a neutropenia
(15'20 "), that is a decrease [reduction] of the white
blood cells - namely certain white blood cells (15'25")
- the neutrophils (15 ' 27''). The
neutrophils are something like the first aid cells of
our body (15'31''), very important in the defense
against pathogens (15'33''). And if after the
vaccination a temporary decrease [reduction] in
neutrophils sets in - at 46% - which is VERY MUCH
(15'43''), then you open a time window after the
vaccination with a weakened immune system compared to
before (15'50''). And because the accumulation of 46%
was so significant, one cannot just ignore it (15'55'').
After all, we are dealing with a vaccine and not with a
drug (16'0''). With a drug, you could perhaps still
accept neutropenia as a side effect (16'4'') because you
are sick (16'6''). The vaccine is administered to
HEALTHY PEOPLE (16'9''). And THEREFORE one CANNOT ACCEPT
that (16'11'').
There are OTHER vaccines, they are rare, but there are
those that can cause neutropenia (16'18''), but always
when they are approved, they provoke neutropenia in the
ONE-DIGIT percentage range (16'22''), but certainly not
at 46 % (16'25'').
AstraZeneca refuses long-term observation with
neutropenia
This is NOT a triviality, and that is something that is
hidden from us everywhere (16'29''). That is really a
serious vaccination side effect (16'33''). This should
lead to - just like the flu-like symptoms (16'37'') -
that long-term monitoring is now being carried out
(16'40''), that long-term observation is now being
carried out - this is called "follow-up phases "
(16'46''). But that is NOT DONE (16'47'').
Criminal "telescoping": Third clinical phase begins
WITHOUT waiting for the result of the first + second
clinical phase!
The vaccine [from AstraZeneca] is already in the third
and final phase (16'50 ") - and as with the preclinical
phase, there is still no final search result
(evaluation) of the first and second clinical phase
(16'59") ).
Because this was only a temporary, a provisional
evaluation report that showed these side effects
(17'6''). Nevertheless, the clinical phase continues
(17'9'').
And you hear in the media, and you also hear from
politicians, and also from the company [AstraZeneca]
itself (17'14 "), that this vaccine might already be
available in autumn (17'18").
Article:
University of Oxford reports breakthrough in corona
vaccine
(orig. German: Uni Oxford
meldet Durchbruch bei Corona-Impfstoff)
At the latest in
spring (17'20'').
Article
of Kurier (Vienna): Corona: "Oxford vaccine" could be
available by the end of 2020
(orig. German: Corona:
"Oxford-Impfstoff" könnte schon Ende 2020 verfügbar
sein)
Ok? Well, it just
comes together too much (17'24'').
Article
by The Washington Post: Oxford coronavirus vaccine
safe and promising, according to early human trial
results published in the Lancet
for the vaccine,
which has already been pre-ordered, also from Austria
and Germany (17'27'')
Article
by UK Express: Oxford COVID vaccine on track for
OCTOBER release ahead of flu season 'Very good
results'
A deficiency,
obviously insufficient effect of the antibodies
(17'32'').
An increased side effect of the vaccination with
symptoms of illness (17'36'').
Mr. Anschober and Mr. Spahn! With THIS
vaccine you send 70% of the vaccinated after the
vaccination on sick leave (17'45''). This is completely
absurd! (17'47'')
Criminal neglect in the AstraZeneca monkey vaccination:
Neutropenia and long-term effects are not clarified!
And: On top of that, this neutropenia, which is not being
adequately investigated now, because - of course one can
always say that was a temporary neutropenia (17'57'') -
but it is very important to note that long-term
observations are necessary here (18 ' 2''). That's why NO
vaccine under 5 years has made it into the approval phase
(18'7''), because you have to observe time-delayed side
effects (18'10''). If a vaccine already shows a
significant accumulation of side effects (18'15''),
-- then you have to consider that it might cause long-term
consequences (18'18'');
-- then you have to consider that it might cause delayed
side effects and vaccination damage (18'24'');
-- then you have to consider that it can have a negative
effect on certain previous illnesses (18'28'');
-- that it may cancel the effect of other vaccines
(18'31'');
-- that it can have interactions and cross-effects with
other medicinal substances (18'35'');
-- that it may be a problem in certain age groups
(18'38''), ok?
-- or with certain previous illnesses (18'41'').
8. The AstraZeneca vaccine is NOT SAFE:
Conclusion: Vaccines UNDER 5 years of development can
NEVER be safe!
All of this would have to be EXTENDED due to this bad side
effect profile and not shortened at all (18'47''). That's
why it is not possible to put a vaccine on the market
under 5 years of development time and then claim it is
safe (18'54'').
9. The lies of the Mossad media:
The Mossad media with lies propaganda for the Oxford
vaccine - the negative benefit-risk profile
Nevertheless, it is said in the media that the vaccine
"would be brilliant" in the clinical phase (19'1'').
Article
in the Pharmaceutical Newspaper (German: Pharmazeutische
Zeitung - PZ): Corona vaccine from Oxford is brilliant
in phase I / II
(orig. German: Corona-Impfstoff
aus Oxford glänzt in Phase I/II)
[Truth is another one]: The vaccine is not brilliant at
all. But it has a DISASTROUS benefit-risk profile
(19'7'').
The aim of vaccine research and the approval process is to
provide empirical evidence (19'13'') that the benefits
clearly outweigh the risks of the vaccine (19'19''). But
that is not the case here, as I said earlier, if only
because of the obviously inadequate effect (19'25'').
How can it be that we don't hear about it in the media
[and] that it is presented to us as a "promising vaccine"?
(19'32'')
The aim of vaccine research and the approval process is to
provide empirical evidence (19'13'') that the
benefits clearly outweigh the risks of the vaccine
(19'19''). But that is not the case here, as I already
explained earlier, first because of having not much effect
at all (19'25'').
How can it be that we don't hear about it in the media
[and] that it is presented to us as a "promising vaccine"?
(19'32'')
10. A primary school teacher (Anschober) +
a bank management assistant (Spahn) go shopping:
The shopping tour WITHOUT a finished product
Austria has ordered 6 million doses of this vaccine
(19'37'').
Article
of Kurier (Vienna): Coronavirus: Austria wants vaccine
for eight million people
(orig. German: Österreich will
Impfstoff für acht Millionen Menschen)
Austria has not ordered any other vaccine so far, only
this one (19'41''). The same with Germany (19'43'').
Article
from "apotheke adhoc": Germany orders AstraZeneca
vaccine (orig. German: Deutschland
bestellt AstraZeneca-Impfstoff)
Germany has ordered 80 million of the Oxford vaccine
(19'47''). The entire EU has already ordered around 400
million (19'51''): Italy, Germany, Austria, the
Netherlands, em, yes, together, and France have ordered
these 400 million doses (20'1'').
As I said, internationally already more than 200 billion
doses - and the vaccine is already being produced
(20'7''). And if someone thinks: Well, that's probably all
right, because the admission offices wouldn't allow that
if there was something wrong with it (20'19''). Then I can
only say: Well, even the pharmaceutical industry knows
that the risk is very high this time (20'24'').
11. The Financial Times warning:
Financial Times with vaccination association "Vaccines
Europe": AstraZeneca lacks the "usual safety data" - the
state should be liable!
In [the] Financial Times a report - a position paper of a
lobby company of the pharmaceutical industry, a lobbying
association - was published (20'36 "), which is called
"Vaccines Europe "(20'39"). And it was written inside that
this time, due to the shortness of the approval
process, it is NOT possible to collect the usual
safety data (20'46''). Well, that's perfectly
clear (20'49''). And that is why this association is now
lobbying that the state or states should assume LIABILITY
for vaccine side effects and vaccination damage (21'0'').
Ok? The newspapers and the media should please report on
it in a big way (21'6 ") - [and] not claim that it's a
"great vaccine", that it's a "safe vaccine" (21'10"), or
that it's "brilliant" (21'11'').
Artikel: The Risks of Rushing a COVID-19
Vaccine. Telescoping testing time lines and approvals may
expose all of us to unnecessary dangers
12. William Haseltine's warning:
William Haseltine: Warning of unknown long-term effects
of AstraZeneca monkey vaccination
Article:
The Risks of Rushing a COVID-19 Vaccine. Telescoping
testing time lines and approvals may expose all of us to
unnecessary dangers
William Haseltine -
the geneticist who was mentioned already before - ALSO
warns of this development (21'17''). He says: The
telescoping of the approval process exposes us all to a
considerable risk (21'26''), because even rare side
effects that are overlooked will be MULTIPLIED by the
application with millions and billions of people (21'37'')
- which is IN PROJECT (21'38'').
The lottery game: Anschober and Spahn have ordered a
highly dangerous AstraZeneca vaccine - the long-term
effects are a lottery game
All of this has NOTHING to do with opposition to
vaccinations, but these are serious concerns that are
raised here (21'45'') and about which people have to be
informed (21'48''). Our Health Minister Anschober [of
Austria] and the German Health Minister Jens Spahn should
please tell people WHAT they bought! (21'55''):
[They bought a medical lottery game!]
a vaccine,
-- the 70% of the vaccinated people on sick leave
(22'2'');
-- which causes neutropenia, i.e. a temporary weakening of
the immune system (22'6'');
-- which opens a time window with an increased risk of
infections (22'10'');
-- and a vaccine that has BIG QUESTION MARKS about its
effectiveness in terms of antibodies and immunity
(22'17'').
13. The criminal mRNA gene vaccinations
have side effects similar to those of AstraZeneca
And it doesn't look much better with the other favorites -
precisely because it's not possible to produce a safe and
effective vaccine in the short time (22'26''). For
example, there are still two RNA vaccines in the pipeline
[the deadly vaccines from Pfizer and Moderna], which
Austria and Germany have NOT pre-ordered (22'33''). That's
why we don't need to go into it that much now (22'35'').
mRNA gene vaccination: neutropenia
But here, too, there was a significant accumulation of
very similar side effects (22'43''). Ok? Which one should
also have to examine in a long-term follow-up (22'47'').
And here too a neutropenia has shown (22'50''). Here, too,
instead of shortening, a longer observation and careful
look is needed for having a safe vaccine (22'59'').
14. RNA anti-cancer drugs are not
comparable:
RNA cancer drugs have a DIFFERENT consideration in
benefit and risk
[Supplement:
90% of cancer cases can be cured with sodium bicarbonate
in water and maple syrup: Cancer cures with 1tsp of
sodium bicarbonate with 3-4 normal spoons of maple
sirup, mix it, take it sober and 2 hours after the last
meal before sleeping, pH8 in the body is rising to pH8
within 12 days, cancer cells transform into normal
cells, tumors collapse - the cure rate is 90%. There
remain 10% of cancer cases where baking soda with maple
syrup does not work and a cancer problem exists - note:
sodium
bicarbonate - note: cancer
healings].
Arvey describes the consideration for RNA cancer drugs:
In addition, there has NEVER been an approved RNA vaccine
against an infectious disease (23'4''). So far there have
only been RNA drugs, for example against cancer (23'9'').
So in oncology there are RNA drugs already in use
(23'12''). But in oncology the balance between benefit and
risk - between side effects and effects is COMPLETELY
DIFFERENT (23'20''), because we are dealing with a
potentially fatal disease (23'23''), so also heavy side
effects are accepted when a healing chance exists
(23'29'').
But this should not be applied for a vaccine fore healthy
people - to millions and billions of healthy people
(23'34''). So this popular lobbying argument that the RNA
vaccines, which are also genetic vaccines, cannot be that
bad because - or that they have already been tested enough
(23'44''), because RNA drugs are used in cancer medicine
(23'49''), this is simply wrong (23'50''). Ok? That cannot
be transferred to vaccine research (23'53'').
There is still so much to say on this subject, you see, I
hardly find an end (23'58''). I will certainly continue to
speak up and would be happy to work with the PPR Institute
(24'5''). Because we now really need a public that
educates seriously and cleanly (24'10''), that means,
public relations that education of the people (24'13'').
We can no longer watch how distorted data is acted on here
(24'19''), with distorted representations, the
misappropriation of evidence that does not correspond to
the government's narrative (24'28''), how the media
continues to do things presenting data in a one-sided way
and in a tendentious way - see the vaccine (24'34'').
There are hardly any reports about these side effects,
hardly any of this failure of the antibodies (24'40'').
There is only reported again and again a good vaccine - a
safe vaccine (24'44'').
15.Oxford makes propaganda with triplets
for a monkey injection:
The propaganda story for the deadly AstraZeneca monkey
injection: from Oxford with Sarah Gilbert with her
triplets
And in the newspaper The Standard, this is an Austrian
daily newspaper, even a "nice story" was presented
(24'51''):
Standard
article: Sarah Gilbert: The "speed queen" of corona
vaccine development (orig. German: Die
"Speed-Queen" der Corona-Impfstoffentwicklung)
Sarah Gilbert, the company founder of this vaccine from
Vaxitech in Oxford, is said to have even included her
triplets in this vaccine study (25'2'') - but these
triplets are grown up already and are studying
biochemistry themselves - maybe they are even in the
vaccine business themselves (25'8''). It is completely NOT
IMPORTANT whether they have got vaccinated or not
(25'13'').
This nice PR story, which obviously comes from a press
release by the company (25'19''), it was spread all over
the world - and again NO WORD could be heard about the
side effects (25'25''), but there was only reported that
the vaccine should be harmless (25'28'').
16. Appeal from Clemens Arvey: add the
withheld data!
And since, as I said, it is simply very important that you
take an opposing position, that you just add what
you DON'T HEAR in the media that, actually I have to
say, is suppressed from us (25'40 '' ). And
that's why I ask you too
-- First of all, thank you for watching the long video to
the end (25'46''), and
-- secondly, I also ask you to share this video (25'50'').
17. Book by Clemens Arvey about
health-ecological perspective + ecological epidemiology:
"We can do better" (orig. German: "Wir können es
besser")
If you would like to find out more about the vaccinations
and also about this health-ecological perspective on
Covid-19 and this ecological epidemiology, which also
exists (26'2''), then you can find out more in my book "We
can do better " ("Wir können es besser") (26'9''). Thank
you for the attention (26'12'').