by Dr. Joseph Mercola
Is This the Biggest COVID Scandal Yet?
$900
Million for Misleading Messaging. exposes troubling details behind the multi-million dollar push for COVID shots, uncovering claims made without evidence and the impact of politicized health directives. How deep does the deception go, and what does it mean for public trust moving forward?
Despite this, the administration launched the "We
Can Do This" Campaign, spending over $900 million to promote vaccine
uptake and public health measures.
Past contracts and fiscal mismanagement within HHS raised red flags about the effectiveness and integrity of their public relations efforts.
As the campaign aimed to shape public behavior
around masking, social distancing and vaccination, the reliance on
flawed Centers for Disease Control and Prevention (CDC) guidance
undermined its credibility.
These early failures were not isolated incidents but part of a broader pattern of inconsistent and politically influenced public health strategies that ultimately eroded the very trust needed to effectively manage a public health crisis.
However, by April 2020, the CDC had completely reversed its stance, recommending masks for everyone outside the home.
This flip-flop was not just confusing but also
seemed politically motivated, influenced by factors such as
teachers' unions pushing for prolonged school closures. 2
This erosion of trust was further exacerbated when breakthrough infections and variants like Delta emerged, proving that earlier mask guidance had been incorrect.
However, this narrative quickly unraveled, as there was no evidence that vaccines prevented transmission.
Despite this, the CDC and the "We Can Do This"
campaign promoted the idea that only vaccinated individuals could
safely forego masks and social distancing.
The administration's insistence that vaccines
stopped transmission contradicted the FDA's original EUA terms and
created a false sense of security.
This disconnect between official statements and
emerging evidence betrayed the public's trust.
You saw federal, state and private employers
enforcing COVID-19 shot requirements, often without clear,
evidence-based justification. These shot mandates targeted millions,
demonstrating the extent of overreach and coercion.
Even vaccine proponents like Dr. Paul Offit criticized the mandates as politically driven rather than grounded in solid public health needs.
The mandates disproportionately affected younger
populations who were already at lower risk of severe illness and
represented an infringement on personal autonomy.
The CDC and HHS launched extensive campaigns targeting parents, using emotionally charged messaging to persuade them to get COVID-19 injections for their young children.
Ads featuring celebrity parents and medical professionals painted a dire picture of COVID-19's impact on children, despite studies showing that,
By emphasizing the need for COVID-19 shots to keep schools open and protect community health, the government leveraged fear and misinformation to drive vaccine uptake.
This approach not only misrepresented the actual
risk but also disregarded the developmental and social impacts of
prolonged masking and school closures on children.
Engaging FMG, HHS aimed to craft a nationwide
multimedia propaganda effort to shape public perception and behavior
regarding COVID-19. 6
This partnership raised significant concerns about the politicization of public health messaging.
Past contracts with FMG had already been
scrutinized for fiscal mismanagement, and this massive investment in
a single campaign further highlighted conflicts of interest and
inefficiencies.
By prioritizing persuasive messaging over
transparent, evidence-based communication, FMG and HHS effectively
prioritized political agendas over scientific integrity.
The use of a private PR firm to drive national
health policies exemplified a troubling shift toward prioritizing
image over substance, undermining the credibility of public health
institutions tasked with presenting accurate information.
Data
Manipulation Included Overcounting Deaths
The recalculation led to a 24% decrease in reported pediatric
deaths, revealing that the initial numbers had been significantly
inflated.
The CDC's admission that 80% of reported errors exaggerated the severity of the COVID-19 situation further eroded trust.
Overall, the report underscores a troubling pattern of inconsistent
messaging, overstated claims and data mismanagement by key public
health authorities during the COVID-19 'pandemic'.
Clinical Trial
Bias Inflated COVID-19 Shot Effectiveness
In randomized controlled trials (RCTs), both
vaccine and placebo groups have synchronized case-counting windows,
ensuring a fair comparison. However, in real-world observational
studies, this window often applies only to the vaccinated group.
Consequently, an entirely ineffective vaccine could misleadingly appear to have substantial effectiveness:
This bias arises because the early post-vaccination period, when individuals are not yet fully protected, is treated differently between groups.
Understanding this flaw is crucial for
interpreting vaccine effectiveness accurately and recognizing that
observational studies may overstate the true benefits of vaccination
due to methodological inconsistencies.
In observational studies, vaccinated individuals are often older and may be less healthy than their unvaccinated counterparts because vaccines were prioritized for those at higher risk.
This imbalance skews results, making vaccines
appear more effective than they truly are.
During periods when overall COVID-19 infection
rates are declining, vaccinated individuals may appear to have lower
infection rates simply because they received the injection during a
peak period.
This temporal mismatch creates a misleading picture of COVID-19 shot effectiveness.
For instance, a decline in cases might be
attributed to vaccination when, in fact, it could be due to other
factors like natural immunity.
COVID Shot
Safety Overstated in Observational Studies
This study highlights that methodological flaws,
such as limited counting windows, lead to an underestimation of
shot-related adverse events.
This exclusion creates a skewed safety profile,
making the shots appear safer than they actually are.
As a result, the true risk associated with vaccines, especially serious conditions like myocarditis, remains obscured.
However, due to the limited adverse effect counting windows in both observational studies and clinical trials, many of these cases went unreported or were misclassified.
Furthermore, rapid unblinding of trials
compromises the ability to monitor long-term safety outcomes,
leaving many important questions unanswered.
Excess Serious
Adverse Events in Pfizer and Moderna Shot Trials
The analysis revealed that both shots were
associated with an excess risk of serious adverse events of special
interest (AESIs) compared to their placebo groups.
When combined, the mRNA vaccines presented a 16%
higher risk of serious AESIs, with a risk difference of 13.2 per
10,000 vaccinated participants.
While the study identified a significant excess
risk of serious adverse events in the Pfizer trial, the FDA
concluded that serious adverse events were "balanced between
treatment groups." 12
The FDA focused on the incidence of participants experiencing any serious adverse event, effectively masking the higher number of multiple adverse events in the shot group.
In contrast, the study accounted for the total
number of adverse events, revealing a more nuanced and concerning
risk profile.
The research analyzed data from 149 countries
between 2001 and 2020, revealing a significant positive association
between disinformation campaigns and the incidence of respiratory
infections.
This correlation underscores how deliberate
dissemination of false information seriously undermines public
health efforts, leading to increased transmission rates and higher
case numbers.
Governments that actively censor information limit the public's access to accurate health data, 15 worsening outcomes as occurred during the 'pandemic'.
As Dr. Robert Malone put it,
The Path
Forward - Ensuring Transparency and Trust in Public Health
In the aftermath of these revelations, the need to advocate for transparency, accountability and evidence-based policies is clear.
The lessons learned from these failures should drive a fundamental
rethinking of how public health campaigns are managed and
communicated, prioritizing scientific data over propaganda to better
serve and protect the public.
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