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For several weeks now, fact-finding commissions have been meeting
in the Bundestag and in various state parliaments to discuss

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“Lessons from the COVID-19 pandemic for the
analysis and review of government measures,” including

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a session held on June 26, 2026, in Brandenburg.

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Below, as representative examples of many other hearings, you
will find some controversial excerpts from attorney Ralf

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Ludwig, an expert on legal matters who was invited to
testify, and Professor Sucharit Bhakdi, a medical expert.

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All of the hearings provide solid evidence of
political, legal, academic, and media misconduct.

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Now the “bigwigs” have had to take note of
this, but will there actually be any consequences?

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This is precisely what needs to be closely monitored.

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After all, if “everything stays the same,” doesn’t that point to
a massive web of collusion—a vicious circle

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involving politicians, the judiciary, scientists and the
media—where, ultimately, one covers for the other?

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“Madam Chair, ladies and gentlemen,
thank you very much for the invitation.”

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I’d like to start with an image that, at first
glance, has nothing to do with COVID-19—aviation safety.

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Let's imagine that several planes crash, and the explanation
that they didn't have enough thrust quickly gains acceptance.

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Then a new type of jet fuel is introduced to the market,
touted as a technological revolution that is expected to

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provide greater safety and protection for the entire fleet.

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In a true culture of safety, this would not be a
time for euphoria, but rather for serious scrutiny.

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No one would say, "The situation is
serious, so let's skip the checklists."

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On the contrary, the more serious the
situation, the stricter the procedure must be.

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And when an airplane crashes, the accident investigation
authority examines every minute detail to determine

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where errors occurred, where manuals, checklists, and
standard procedures were followed, and where they were not.

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And if not, what was the reason for deviating from it?

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We should apply this standard to our pandemic policies as well.

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Germany wasn't without a plan at the beginning of 2020.

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The national pandemic plan, which was updated in March 2020 to
include a threat scenario involving the novel

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coronavirus, outlines structures, measures, and
recommendations for preparing for and managing a pandemic.

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It was intended to help slow the spread of a new
virus and reduce the number of illnesses and deaths.

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The measures later implemented on a
widespread basis with regard to the general public

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were specifically not provided for in that plan.

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Nevertheless, measures were adopted at the conferences of
state premiers with the chancellor that deviated from this plan.

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What was surprising was that it was those who demanded
adherence to the plan who had to justify themselves, rather than

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those who should have had to explain any deviations from it.

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In the context of flight safety, this means that anyone who
deviates from an existing emergency plan or manual must openly

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justify the deviation with sound reasoning and document it.

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As the leaked RKI records have shown, and as has already been
presented here in this committee, these

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justifications were mostly politically motivated
and therefore not based on sound reasoning.

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But today's topic isn't masks or lockdowns—it's vaccination.

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How is a novel vaccine approved? Standard approval is the norm.

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Prior to approval, a largely complete dossier must be
submitted—covering quality, manufacturing, composition,

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control, stability, nonclinical safety, clinical efficacy,
clinical safety, pharmacovigilance and risk management.

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The agency may only grant approval if
the risk-benefit analysis is positive.

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Then there is what is known as conditional admission.

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Conditional approval is a statutory exception.

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It allows for earlier approval, even
though not all data is available yet.

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However, the requirements for conditional approval include, in
particular, a positive benefit-risk balance, an unmet medical

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need, the expected ability to subsequently
provide missing data, and an immediate benefit that

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outweighs the risks associated with the data gaps.

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Comirnaty and the other vaccines were
initially granted this type of conditional approval.

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For pregnant women, breastfeeding women,
immunocompromised individuals, and other special

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populations, there were only limited or no direct data.

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The vaccine used in the efficacy study was
different from the one used to assess

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distribution, metabolism, and excretion in the body.

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Comparative and substitute data were evaluated. The final clinical
trial report for the pivotal study was also not available.

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The critical issue is that, at many points in the
approval process there were deviations from the

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procedure prescribed by law or exceptions were granted.

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Policymakers and the public—and later the doctor administering
the vaccine—should have taken into account that the approval was

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initially conditional and that key questions, such as
the duration of protection, transmission , protection

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of others, etc., had not been conclusively answered.

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For the legal and political assessment, therefore, it is not only
the fact that STIKO issued a recommendation that is decisive.

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The key factor is whether the process
leading up to that point is properly documented.

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Appropriate questions, a systematic literature search,
GRADE assessment , transparent presentation, low-quality

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evidence, and a clear rationale for the recommendation.

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Several safety-related endpoints were rated
only as “very low” in the GRADE profile—such

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as miscarriage, stillbirth, and preterm birth.

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If the recommendation were to cover fetal and neonatal safety as
well, it would have been necessary to conduct visible testing

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to determine whether vaccine components, lipid nanoparticles,
mRNA, or spike proteins can reach or cross the placenta.

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So, the checklists were not followed.

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Nevertheless, STIKO continues to maintain that
there are no safety concerns for pregnant women.

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Despite all the shortcomings that have been pointed out—the lack
of proper implementation of the processes, the lack of research

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data, and the safety concerns that are regularly raised— as also
pointed out today by Prof. Dr. Bhakdi, the

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state of Brandenburg still recommends vaccinating
pregnant women with mRNA vaccines—even today.

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Responsibility for the people does not lie with the EMA or
STIKO, but with the Ministry of Health here in Brandenburg

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and, ultimately, with each doctor administering the vaccine.

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While the person authorizing takeoff may rely on specialist
departments, if there are specific indications of

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safety concerns, that person is personally responsible for
keeping the aircraft on the ground. Thank you very much.”

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Although STIKO has since withdrawn its vaccination recommendation
for healthy pregnant women, it has not yet

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issued a general warning about the sometimes
devastating consequences of mRNA injections.

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“Good morning, ladies and gentlemen. I was
born in Washington, D.C., after the war.”

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My father was a diplomat at the embassy there.

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In the decades that followed, my father
served as Thailand's ambassador to

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Switzerland, North Africa, and the Benelux countries.

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I spent my school years in Bern, Cairo, and Bangkok, and came to
Bonn in 1963 to study medicine. I received my doctorate in 1970.

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After that, I began my research at the Max
Planck Institute for Immunobiology in Freiburg.

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That was followed by work at the Institute of
Medical Microbiology at the University of

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Giessen for my habilitation and a professorship.

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In 1985, I was appointed director of the Institute
of Microbiology at the University of Copenhagen.

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In 1990, I accepted the position of director of the Institute
of Medical Microbiology and Hygiene at the University of Mainz.

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There in Mainz, a close collaboration developed
with the State Chancellery and the State Parliament.

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In the wake of the SARS pandemic, we organized a two-day
informational event for the general public 23 years ago.

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By the way, the program is included in my autobiography.

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In the heart of the city, Minister President Kurt Beck
and members of the state parliament met with us to discuss

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issues related to the topic “Future Infection Threats.”

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The event was extremely beneficial for everyone.

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Two years later, I was awarded the Order of
Merit of the State of Rhineland-Palatinate.

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Today, 23 years later, I find myself surrounded by
members of the state parliamentfor the second time.

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I hope for nothing more than that our
collaboration will bear similar fruit.

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Ladies and gentlemen, there are documents that will
serve as evidence before the judgment seat of God:

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First, the COVID-19 pandemic was conceived
and fabricated years before 2020; its course

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and the measures to be taken were planned.

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The climax was the approval of the gene-based
vaccines and their administration to the world's population.

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Second, the BioNTech vaccine paved the way.

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It was hailed as an effective and reliable
savior in the midst of apocalyptic distress.

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The vaccine has never been tested for efficacy and safety.

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The evidence of efficacy submitted to the
regulatory authorities was simply fabricated and false.

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In its records dated April 27,
2020, the Robert Koch Institute stated:

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The mass human experiment had been
carefully planned from the very beginning.

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Third, while the U.S. emergency use authorization and its
equivalent here—conditional approval—do permit the use of

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substances that have not been rigorously tested, but under no
circumstances is it permitted to do what was initiated

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during the COVID-19 crisis: the injection of
substances with documented toxic effects into healthy people.

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Fourth, who hasn’t heard about Bill Gates’ historic appearance,
when he announced in Merkel’s presence: “We will protect

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seven billion global citizens with the vaccine”—from what?

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From the specter we have created ourselves. But
if not to protect against that, then what else?

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The simple answer: for power and money—an
endless amount of money that is taken from us and

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flows into the pockets of the master planners.

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But now the time for change has come, ladies and gentlemen.

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You should all know this: mRNA vaccines have to be encapsulated
so that they can be transported through our bodies to our cells.

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Otherwise, they would be broken down by enzymes.

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The protective cover contains synthetic,
man-made substances whose use on healthy people was

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prohibited for medical reasons prior to 2020.

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Now hold on tight. Two years ago, it was
discovered that these substances have a lethal property.

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The same characteristic that bacteria
exhibit in cases of blood poisoning. What happens?

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An explosive activation of the immune system.

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An explosion of inflammatory centers
wherever the billions of particles end up.

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And they end up everywhere,
because there are no barriers for them.

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The blood-brain barrier and the
placental barrier do not exist for them.

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But billions of sites of inflammation—that is, inflammation
of the brain, heart, liver, lungs, and kidneys—damage

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everywhere, with irreparable damage to the heart and brain.

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And this happens even before the gene vaccine enters
the cells and unleashes its own horrendous effects there.

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Ladies and gentlemen, this discovery should have
led to an immediate ban on these so-called vaccines!

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Tolerating blood poisoning from a
vaccination? What would that be?

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What was that? What is it now, here and today?

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A capital offense, ladies and gentlemen.

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Keep in mind: In mid-2020, BioNTech developed a safe and
effective vaccine that passed the required clinical

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trials and received conditional approval in December 2020.

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However, von der Leyen's binding pre-order for
hundreds of millions of vaccine doses came well before

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that—in November, specifically in early November 2020.

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In a shrewd move, the manufacturing process
was quietly modified as early as October 2020.

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The original process was actually very
expensive, whereas the modified one was dirt cheap.

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In other words, a different product was supplied and
administered from the one tested in the clinical trials.

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That, ladies and gentlemen, is fraud.

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This isn't just about billions—it's a massive fraud.

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It was—and still is—a matter of
human lives! Now listen carefully.

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In the process, which was secretly modified,
genetically modified bacteria and

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minichromosomes—known as plasmids—were and continue to be used.

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However, their use created an insurmountable problem: namely,
it was—and remains—impossible to completely remove the bacterial

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chromosomes from the vaccine during the production process.

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As a result, remnants of these chromosomes have been
analyzed in various laboratories over the past three

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years and have been found in different vaccine batches.

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And know this: scientific findings have been documented:

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First, bacterial chromosome fragments can be
incorporated into human chromosomes and cause cancer.

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Second, the vaccine throws a wrench
into the entire genomic machinery.

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Nothing works properly anymore in the affected cells.

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The outcome for health and life can be whatever the devil wants.

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Third, the foreign gene that has been
introduced remains in the body for a long time.

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Ladies and gentlemen, the genome is the totality of all genes.

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Any change to this whole is a genetic modification—so
vaccinated people remain genetically modified for a long time.

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Fourth, the vaccine triggers self-attacks and
self-destruction in all organs from head to toe.

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Fifth, the vaccine passes through the placenta to the fetus.

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Ladies and gentlemen, mRNA vaccines are the most
dangerous medical substances ever created by human hands!

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Their marketing was—and continues to be—based on
the supply of a product that differs from the

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substance that was actually tested in the clinical trials.

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It's unbelievable—not a single mRNA vaccine currently on
the market has ever been tested in a proper clinical trial.

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The essential requirement for approval simply
does not exist. How could all of this be possible?

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Ladies and gentlemen, the COVID-19 vaccine
is the greatest medical crime of all time!

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Who's behind this? Certainly not any of us here.

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No one could have even begun to guess the truth.

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In fact, the answer came just last week from the
highest levels of the U.S. intelligence service:

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The virus and the vaccine were developed in biological
weapons laboratories in China and the United States.

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Yes, you heard that right. And the main
perpetrators and accomplices have been identified by name.

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Of course, none of us are involved. No, we are
all the victims—all of us—victims of the first

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monstrous biological weapons attack on humanity.

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Ladies and gentlemen, in 1989 a movement began in
Leipzig that led to the greatest miracle of that time.

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I witnessed it from a distance and cried with gratitude.

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Dear friends, let us now set out together on this journey, with
our eyes fixed on a single goal: the reunification of humanity.

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"I am grateful to fate for allowing me to be here with
you today in Potsdam. May you be blessed, and goodbye."

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Despite these compelling arguments presented by
Ralf Ludwig, Professor Bhakdi, and many others,

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there have been no far-reaching consequences to date.

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So far, there have been no serious consequences for politicians
whose decisions during the COVID-19 pandemic contributed to a

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great deal of suffering—ranging from severe vaccine-related
injuries and economic damage up to the bankruptcies of

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small businesses, etc.— nor is there any investigative
reporting on the issue in the so-called mainstream media.

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On the contrary, for example, the *Deutsches
Ärzteblatt* on July 2, 2026, and *Deutschlandfunk* on July 4,

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2026, were actually singing the praises of mRNA vaccines.

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They are said to offer effective protection
against infection, severe illness, and death.

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If, despite many clear statements made during the hearings of the
fact-finding commissions, neither the media, nor politicians, nor

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the judiciary take action, it reinforces the
suspicion that there is collusion among these sectors and

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that a vicious cycle is unfolding right before our eyes.

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