Pfizer CEO Albert Bourla has made “misleading” and unsubstantiated statements on the merit of giving COVID-19 vaccines to young children, according to a case report published by a UK pharmaceutical watchdog on Jan. 27.
During an interview with the BBC published on Dec. 2, 2021, Bourla was asked whether he believed it was likely that 5- to 11-year-olds in the UK and Europe would be vaccinated against COVID-19 and whether it was a good idea.
The interview was published after the U.S. Food and Drug Administration authorised the use of the Pfizer-BioNTech COVID-19 vaccine for young children, but the UK’s medicines regulator, the Medicines and Healthcare products Regulatory Agency (MHRA), didn’t approve the product for the same age group until Dec. 22, 2021.
While acknowledging that it was up to the UK authorities to decide whether or not to approve and deploy the vaccines, Bourla replied, “I believe it’s a very good idea.”
He cited disruptions in education and the potential of developing so-called long-COVID, saying, “so there is no doubt in my mind about the benefits completely are in favour of doing it.”
Syringes in front of displayed Biontech and Pfizer logos on Nov. 10, 2020. (Dado Ruvic/Illustration/Reuters)
Following complaints from UsForThem—a children’s welfare campaign group founded in response to the COVID-19 lockdowns—a panel from the Prescription Medicines Code of Practice Authority (PMCPA) ruled that Bourla’s statements breached a number of rules in the Association of the British Pharmaceutical Industry (ABPI) code of practice.
After Pfizer appealed against the ruling, an appeal board upheld five counts of breaches of three ABPI codes that require information and claims to be accurate, balanced, capable of substantiation, not raising unfounded hopes of successful treatment, and not be misleading with respect to the safety of the product.
The PMCPA described Bourla’s statements as being of a “strong unqualified nature.” It also said they inferred there was “no need to be concerned about potential side-effects of vaccination in healthy children aged 5-11” and that the implication was “misleading and incapable of substantiation.”
The PMCPA said it has received an undertaking from Pfizer to prevent similar breaches in the future.
Code breakers are charged for administrative costs, but the self-regulatory body does not have the power to impose fines or other legal sanctions.
Bourla was initially found to have also breached the code for promoting the Pfizer-BioNTech vaccine in the 5–11 age group when it was not authorised by the MHRA, but the appeal board overturned the ruling, agreeing with Pfizer that its CEO was asked a specific question and it was not unreasonable to talk about the issue in principle. The board also noted that two other COVID-19 vaccines were also under investigation for the age group.
The appeal board also overturned previous rulings that said Pfizer had failed to maintain high standards and brought discredit upon the industry.
Most Serious Rulings
Pfizer didn’t respond to The Epoch Times’ request for comment. In a previous statement to The Telegraph in November 2022, when the newspaper obtained the unpublished ruling, a spokesman for Pfizer said the company was “committed to the highest levels of integrity in any interaction with the public.”
“We are pleased the UK’s PMCPA Appeal Board found Pfizer to have maintained high standards and upheld confidence in our industry, the two most serious rulings in this complaint from a UK campaign group,” the statement reads.
“In the UK, we have always endeavoured to follow the principles and letter of our industry Code of Practice throughout. We will review the case report in detail when we receive it, to inform future activity,” it added.
Speaking to The Epoch Times on Tuesday, Ben Kingsley, head of legal affairs at UsForThem, said he was “thrilled” the regulator ultimately agreed with them that the Pfizer CEO’s statements were misleading and unsubstantiated after the pharmaceutical giant opposed their claims “with all of the resources at its disposal” throughout the process.
Commenting on Pfizer’s previous statement on the ruling, Kingsley said the group “found it quite surprising” that Pfizer would consider the rulings about maintaining high standards and upholding confidence in the industry the “most serious” of all.
“I think to the average member of the public, we’d regard misleading us about the safety of their product to be plenty more serious than bringing the repute of the pharmaceutical industry down,” he said.
“So I think it tells you something about the mindset and the priorities of pharma executives that they regard the abuse of the industry as being a more serious matter than misleading the public.”
(L-R) Professor Wei Shen Lim, chair of JCVI’s COVID-19 subcommittee; Professor Jonathan Van Tam, deputy chief medical officer for England; and Dr. June Raine, chief executive of the Medicines and Healthcare products Regulatory Agency, attend a media briefing at Downing Street Briefing Room in London on Nov. 29, 2021. (Stefan Rousseau/WPA Pool/Getty Images)
n June 2021, the UK government’s advisory body on vaccines, the Joint Committee on Vaccination and Immunisation (JCVI), declined to recommend COVID-19 vaccines for healthy children aged between 12 and 15, given the “marginal” benefits young teens would get from the vaccines and the lack of long-term data on the side-effects, including myocarditis.
But the vaccines were later offered to the age group after UK chief medical officers made a recommendation based on wider considerations, including the disruption to children’s education—attributed by some to COVID-19 and by others to the political decision to make children who test positive stay out of school.
The JCVI later recommended a one-off “non-urgent offer” to vaccinate 5- to 11-year-olds. The offer ended in August last year.
In is most recent recommendation, the JCVI said under–50s who are at lower risk of getting seriously ill with COVID-19 will soon be unable to get a booster shot. The offer of primary doses will also end for low-risk people in all age groups.
Resource of Article: Pfizer CEO Made ‘Misleading’ Statements on Vaccinating Children Against COVID-19: UK Watchdog
SearchHamburgerPfizer Signs Agreement to Provide the European Union with PAXLOVID™Wednesday, November 23, 2022 – 11:00amShare
• New agreement to supply up to 3.4 million treatment courses to countries across Europe; this deal supplements the courses provided to 17 EU member states under existing bilateral agreements • Deliveries to participating countries commencing imminently NEW YORK, November 23, 2022 — Pfizer Inc. (NYSE: PFE) today announced an agreement with the European Commission (EC) to supply its COVID-19 oral therapy, PAXLOVID™ (nirmatrelvir [PF-07321332] tablets and ritonavir tablets) to countries participating in the Joint Procurement Agreement across Europe. This agreement, negotiated with the Health Emergency Preparedness and Response Authority (HERA) of the EC, is in addition to the bilateral agreements Pfizer has previously signed with 17 EU Member States. This agreement will supply participating countries up to 3.4 million treatment courses upon orders being placed. Under the terms of the agreement, Pfizer will begin delivery of the initial treatment quantities ordered by the participating countries in November, in parallel to deliveries underway as part of existing bilateral agreements.“Clinical data and real-world evidence for PAXLOVID have shown that it can be an important tool in helping to reduce hospitalizations and deaths in those at increased risk of serious illness from COVID-19,” said Albert Bourla, Chairman and Chief Executive Officer, Pfizer. “As the region prepares for winter and a possible resurgence in COVID-19 infections, the accessibility and availability of treatment options is of the utmost importance. We are pleased to be working with the European Commission to make PAXLOVID available to more patients across Europe.”PAXLOVID is currently authorized for conditional or emergency use in more than 70 countries across the globe. Following the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) positive opinion to authorize PAXLOVID, a conditional marketing authorization (CMA) for PAXLOVID was granted in January 2022 for the treatment of COVID-19 in adults who do not require supplemental oxygen and who are at increased risk of the disease becoming severe. Europe plays a critical role in the delivery of PAXLOVID to patients across the globe, as the site of four of Pfizer’s key PAXLOVID manufacturing facilities.About PAXLOVID™ (nirmatrelvir [PF-07321332] tablets and ritonavir tablets) PAXLOVID is a SARS-CoV-2 main protease (Mpro) inhibitor (also known as SARS-CoV-2 3CL protease inhibitor) therapy. It was developed to be administered orally so that it can be prescribed early after infection, potentially helping patients avoid severe illness (which can lead to hospitalization and death). Nirmatrelvir [PF-07321332], which originated in Pfizer laboratories, is designed to block the activity of the Mpro, an enzyme that the coronavirus needs to replicate. Co-administration with a low dose of ritonavir helps slow the metabolism, or breakdown, of nirmatrelvir in order for it to remain active in the body for longer periods of time at higher concentrations to help combat the virus.Nirmatrelvir is designed to inhibit viral replication at a stage known as proteolysis, which occurs before viral RNA replication. In preclinical studies, nirmatrelvir did not demonstrate evidence of mutagenic DNA interactions.Current variants of concern can be resistant to treatments that work by binding to the spike protein found on the surface of the SARS-CoV-2 virus. PAXLOVID, however, works intracellularly by binding to the highly conserved Mpro (3CL protease) of the SARS-CoV-2 virus to inhibit viral replication. Nirmatrelvir has shown consistent in vitro antiviral activity against the following variants: Alpha, Beta, Delta, Gamma, Lambda, Mu, and Omicron BA.1, BA.2 and BA.4.PAXLOVID is generally administered at a dose of 300 mg (two 150 mg tablets) of nirmatrelvir with one 100 mg tablet of ritonavir, given twice-daily for five days. One carton contains five blister packs of PAXLOVID, as co-packaged nirmatrelvir tablets with ritonavir tablets, providing all required doses for a full five-day treatment course.Our Commitment to Access Pfizer is committed to working toward equitable access to our oral COVID-19 treatment, PAXLOVID, for high-risk patients in need, aiming to deliver safe and effective oral treatment as soon as possible and at an affordable price. If authorized or approved, during the pandemic, Pfizer will offer its oral therapy through a tiered pricing approach based on the income level of each country to promote equity of access across the globe; high and upper-middle income countries will pay more than lower-income countries. Pfizer has established a comprehensive strategy in close partnership with worldwide governments, international global health leaders, including WHO’s Access to COVID-19 Tools Accelerator (ACT-A), and global manufacturers to optimize supply and access of PAXLOVID all around the world. This includes:
Multilateral Supply Agreements: Agreements in place with UNICEFfor the supply of up to 4 million treatment courses to 137 low- and middle-income countries and with Global Fund for up to 6 million treatment courses for supply to 132 Global-Fund grant-eligible countries, subject to regulatory approval or authorization.Expanding Access to Patent-Protected Medicines in Lower-Income Countries: Launched An Accord for a Healthier World, a first-of-its-kind initiative to enable sustained, equitable access to high-quality medicines and vaccines for 1.2 billion people living in lower-income countries. Pfizer has committed to provide its patent-protected medicines and vaccines available in the U.S. or European Union, including PAXLOVID, on a not-for-profit basis to 45 lower-income countries around the world and will collaborate with government and global health leaders to address barriers that limit access beyond supply, like diagnosis, education, infrastructure, storage and more.Accelerating Testing and Treatment: Joined the COVID Treatment Quick Start Consortium, a joint initiative implemented by Duke University, the Clinton Health Access Initiative (CHAI), COVID Collaborative and Americares with support from Pfizer, Open Society Foundations and the Conrad Hilton Foundation. Pfizer will provide treatment courses of PAXLOVID, as well as financial support, to support the Consortium’s efforts to accelerate COVID-19 testing and improve access to treatments in under-resourced parts of the world. The consortium has launched test and treat initiatives in partnership with ten countries in Africa and Southeast Asia. Humanitarian Treatment Donation: As part of its humanitarian response, Pfizer donated 200K treatment courses of PAXLOVID to Ukraine.Voluntary Licensing: Signed a voluntary license agreement with Medicines Patent Pool (MPP) to enable the development and distribution of generic versions of Pfizer’s oral treatment to further expand long-term global supply and access. MPP has signed sublicense agreements with 38 manufacturers, who will supply the generic versions in 95 low- and lower-middle-income countries.
U.S. FDA Emergency Use Authorization Statement PAXLOVID has not been approved, but has been authorized for emergency use by FDA under an EUA, for the treatment of mild-to-moderate COVID-19 in adults and pediatric patients (12 years of age and older weighing at least 40 kg) with positive results of direct SARS CoV-2 viral testing, and who are at high-risk for progression to severe COVID-19, including hospitalization or death. The emergency use of PAXLOVID is only authorized for the duration of the declaration that circumstances exist justifying the authorization of the emergency use of drugs and biological products during the COVID-19 pandemic under Section 564(b)(1) of the Act, 21 U.S.C. § 360bbb-3(b)(1), unless the declaration is terminated or authorization revoked sooner.AUTHORIZED USE The U.S. Food and Drug Administration (FDA) has issued an Emergency Use Authorization (EUA) for the emergency use of the unapproved product PAXLOVID for the treatment of mild-to-moderate coronavirus disease 2019 (COVID-19) in adults and pediatric patients (12 years of age and older weighing at least 40 kg) with positive results of direct severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) viral testing, and who are at high risk for progression to severe COVID-19, including hospitalization or death.LIMITATIONS OF AUTHORIZED USE
PAXLOVID is not authorized for initiation of treatment in patients requiring hospitalization due to severe or critical COVID-19PAXLOVID is not authorized for use as pre-exposure or post-exposure prophylaxis for prevention of COVID-19PAXLOVID is not authorized for use for longer than 5 consecutive days
PAXLOVID may be prescribed for an individual patient by physicians, advanced practice registered nurses, and physician assistants that are licensed or authorized under state law to prescribe drugs.
PAXLOVID may also be prescribed for an individual patient by a state-licensed pharmacist under the following conditions:
Sufficient information is available, such as through access to health records less than 12 months old or consultation with a health care provider in an established provider‑patient relationship with the individual patient, to assess renal and hepatic function; and Sufficient information is available, such as through access to health records, patient reporting of medical history, or consultation with a health care provider in an established provider‑patient relationship with the individual patient, to obtain a comprehensive list of medications (prescribed and non-prescribed) that the patient is taking to assess for potential drug interaction.
The state-licensed pharmacist should refer an individual patient for clinical evaluation (e.g., telehealth, in-person visit) with a physician, advanced practice registered nurse, or physician assistant licensed or authorized under state law to prescribe drugs, if any of the following apply:
Sufficient information is not available to assess renal and hepatic function.Sufficient information is not available to assess for a potential drug interaction.Modification of other medications is needed due to a potential drug interaction.PAXLOVID is not an appropriate therapeutic option based on the authorized Fact Sheet for Healthcare Providers or due to potential drug interactions for which recommended monitoring would not be feasible.
PAXLOVID is not approved for any use, including for use for the treatment of COVID-19.
PAXLOVID is authorized only for the duration of the declaration that circumstances exist justifying the authorization of the emergency use of PAXLOVID under 564(b)(1) of the Food Drug and Cosmetic Act unless the authorization is terminated or revoked sooner.IMPORTANT SAFETY INFORMATION PAXLOVID is contraindicated in patients with a history of clinically significant hypersensitivity reactions (eg, toxic epidermal necrolysis [TEN] or Stevens-Johnson syndrome) to its active ingredients (nirmatrelvir or ritonavir) or any other components of the product. Drugs listed in this section are a guide and not considered a comprehensive list of all drugs that may be contraindicated with PAXLOVID. The healthcare provider should consult other appropriate resources such as the prescribing information for the interacting drug for comprehensive information on dosing or monitoring with concomitant use of a strong CYP3A inhibitor such as ritonavir. PAXLOVID is contraindicated with drugs that are highly dependent on CYP3A for clearance and for which elevated concentrations are associated with serious and/or life-threatening reactions:
PAXLOVID is contraindicated with drugs that are potent CYP3A inducers where significantly reduced nirmatrelvir or ritonavir plasma concentrations may be associated with the potential for loss of virologic response and possible resistance. PAXLOVID cannot be started immediately after discontinuation of any of the following medications due to the delayed offset of the recently discontinued CYP3A inducer:
There are limited clinical data available for PAXLOVID. Serious and unexpected adverse events may occur that have not been previously reported with PAXLOVID use. Risk of Serious Adverse Reactions Due to Drug Interactions: Initiation of PAXLOVID, a CYP3A inhibitor, in patients receiving medications metabolized by CYP3A or initiation of medications metabolized by CYP3A in patients already receiving PAXLOVID, may increase plasma concentrations of medications metabolized by CYP3A. Initiation of medications that inhibit or induce CYP3A may increase or decrease concentrations of PAXLOVID, respectively. These interactions may lead to:
Clinically significant adverse reactions, potentially leading to severe, life-threatening, or fatal events from greater exposures of concomitant medicationsClinically significant adverse reactions from greater exposures of PAXLOVIDLoss of therapeutic effect of PAXLOVID and possible development of viral resistance
Consult Table 1 of the Fact Sheet for Healthcare Providers for clinically significant drug interactions, including contraindicated drugs. Drugs listed in Table 1 are a guide and not considered a comprehensive list of all possible drugs that may interact with PAXLOVID. Consider the potential for drug interactions prior to and during PAXLOVID therapy; review concomitant medications during PAXLOVID therapy and monitor for the adverse reactions associated with the concomitant medications.Anaphylaxis and other hypersensitivity reactions have been reported with PAXLOVID. Cases of Toxic Epidermal Necrolysis and Stevens-Johnson syndrome have been reported with ritonavir, a component of PAXLOVID (refer to NORVIR prescribing information). If signs and symptoms of a clinically significant hypersensitivity reaction or anaphylaxis occur, immediately discontinue PAXLOVID and initiate appropriate medications and/or supportive care.Hepatotoxicity: Hepatic transaminase elevations, clinical hepatitis, and jaundice have occurred in patients receiving ritonavir. Therefore, caution should be exercised when administering PAXLOVID to patients with pre-existing liver diseases, liver enzyme abnormalities, or hepatitis. Because nirmatrelvir is co-administered with ritonavir, there may be a risk of HIV-1 developing resistance to HIV protease inhibitors in individuals with uncontrolled or undiagnosed HIV-1 infection.Adverse events in the PAXLOVID group (≥1%) that occurred at a greater frequency (≥5 subject difference) than in the placebo group were dysgeusia (6% and
Pfizer and Clear Creek collaborate on SARS-CoV-2 PLpro inhibitors for COVID-19
Microscope and coronavirus illustration
Dec. 7, 2022
Pfizer Inc. and Clear Creek Bio Inc. have entered into a research collaboration and exclusive license agreement to advance the discovery and development of potential inhibitors of the SARS-CoV-2 papain-like protease (PLpro) for the oral treatment of COVID-19. PLpro is an essential enzyme, which, along with the main protease (Mpro), plays an important role in viral replication. Under the agreement, the two companies will work together to identify a PLpro candidate to progress into the clinic, at which time Pfizer will be solely responsible for further development and commercialization activities. Clear Creek Bio will receive an undisclosed upfront payment and will be eligible to receive additional potential milestone payments plus royalties on future product sales (Pfizer News Release).
We are witnessing crimes against humanity taking place all across this country and all over the world. Our friends and family members have been and are being harmed by measures ostensibly implemented to protect them and keep them safe.
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Click link to document your story in the COVID-19 HUMANITY BETRAYAL MEMORY PROJECT.
We are witnessing crimes against humanity taking place all across this country and all over the world. Our friends and family members have been and are being harmed by measures ostensibly implemented to protect them and keep them safe.
Two Years of Isolation, Abuse & Mistreatment
For over two years, the people have been abused, manipulated, maligned, and sometimes even murdered in the name of public health. This has been and is still going on in hospitals, assisted living facilities, juvenile detention centers, schools, and really anywhere else that institutional mandates can be applied with force. We, the people harmed by these unamerican and unconstitutional measures, are dedicated to pushing back on this encroachment on our civil liberties, and putting a stop to these grievous harms the people are being forced to endure at the hands of those entrusted to protect them.
Never Forget
This is one of many projects developed to defend our liberties undertaken by the FFFF. The primary goal of this project is to document, archive, and assist those impacted by these crimes against humanity. We are taking testimonials from those who have survived the protocols mandated by these disastrous policies, interviewing victims and family members to validate their stories, and documenting and archiving everything. We will not allow the victims of these crimes against humanity to go unheard.
Managed By FFFF Citizens Task Force
The FFFF Task Force is composed of survivors, victims, and families of victims who have suffered grievous harm as a result of malicious public health policy. If you have been harmed by the disastrous public health policies of the last two years and would like to help others and raise awareness, please Join the FFFF Task Force today.
Another day, another tragedy. It’s become an all-too-familiar story by now.
Her doctor, her government and the mainstream media – all assured her it would be OK, and that the new experimental mRNA synthetic pharmaceutical cocktail was ‘safe and effective.’ In a mere moment, her entire life turned on a dime.
Just 12 hours after receiving her experimental COVID-19 gene therapy injection manufactured by Pfizer, 33-year-old mother Rachel Cecere’s body began rebelling against her, and she was later diagnosed with “acute distress to the nervous system.” Rachel found herself paralyzed from the neck down, but three weeks later she was able to regain strength in her upper body, except for her left hand.
The timing of the onset of her disease just after receiving the experimental ‘vaccine’ is suspect to say the least. Was her disability brought on by the jab? If so, who will be held accountable?
She is not alone either. To date the various vaccine adverse reactions databases in the US, UK, and EU alone contain, on the aggregate, millions of reported injuries, as well as tens of thousands of deaths following the experimental shot.
She asks in desperation, “When is this going to get better?” Watch:
By now, you’ve likely seen many of your friends and family posting about conspiracy theories tied to vaccines, Bill Gates, and New World Order. If you’re anything like me you might be asking the question, “why are so many people off their rocker?”. Today, I’m going to share with you what I’ve learned about why some folks have concerns in these areas. My hope is to genuinely educate you on things that weren’t so obvious to me, that have since given me empathy and understanding for a whole group of people and causes that were otherwise not on my radar.
OVERVIEW
Bill Gates and Tedros, WHO
I’ve come to understand at least 3 major reasons people might have concerns about vaccines:
Health concerns:
Volume of vaccines
Volume of vaccine dosages
Vaccine schedules
Combination Vaccines
Ethical concerns:
Fetal tissue
Vaccine approval rigor
Vaccine trade-off value
Vaccine mandates
Vaccine producers’ lack of financial/legal liability for vaccine injuries
Vaccine as population control
Economic concerns:
Tax dollars fund Vaccine Injury Programs
Big Pharma Profiteering
ANTI-VAXXERS
When most people hear about “anti-vaxxers” they tend to think of crazy people spewing all over the camera with their grotesque pictures of aborted babies, shouting angrily about MCR-5 and vaccine injuries. Because this is what we see, we’ve been dismissive towards the rest of the anti-vaxxer movement, who is a little more…subtle.
There are highly intelligent, well-mannered, respected, professional folks who have legitimate concerns about vaccines. But finding these people is like working through a level 100 Where’s Waldo puzzle. Where are they? And why don’t we hear from them? Two reasons: (1) they don’t want to be associated with the crazy people, and (2) if someone hears that they have any reservations about vaccines whatsoever, they immediately attack them with questions like, “people used to die from polio, do you really want that back, do you?!”. As you can imagine, that’s not a great opener for engaging any reasonably-minded person in a well-respecting debate. Effectually, it’s actually quite difficult to learn about the very legitimate concerns that do exist about vaccines, because the folks who might take the time to help you understand are too apprehensive that you might judge and condemn them.
MY LOVE OF SCIENCE, MATH AND LOGIC
I grew up knowing vaccines are good. I got my vaccines on schedule. I carried around my vaccination card like a well-earned A+ report card. I kept an eye on when certain vaccines were expiring and would promptly go get a new one at the right time.
Since I was four years old, I knew two things: I wanted to build computers and be a doctor. At the age of four, I built my first computer with my dad (and have gone on to build many computers since then). But medicine in particular always had my interest above math. I was fascinated by medicine. In high school, I went through a Health Science Academy for four years,which enabled me to get Pharmacy Tech certified and CNA certified. I learned every medical prefix and suffix in the book (literally), and even spent two years learning Latin to help me better understand medical terminology. To earn my Pharmacy Technician certification, I went through two years of courses in 11th and 12th grade, and was examined by the state of Texas. I had to learn about all classes of drugs, and also vaccines. I went through many internships, at Pharmacies, at a Maxiofacial surgeon, at a retirement care community, and in all wings of the hospital, from ER, to post-op, to NICU, ICU, etc.
I proceeded to go to premed school, and was enthralled by human biology, anatomy, medicine, and the likes. I actually made the study guides in all my classes for my peers. They’d go on to make A’s on every test for which they used my guide. After a year at premed, I actually realized this wasn’t the call God had on my life (which was quite disorienting, considering I had spent the last 5 years dedicated to premed programs, and had spent the last 16 years knowing I would be a doctor).
I pulled out of med school and found my way to Psychology, wherehe . My teachers would give me essay assignments with requirements like “minimum 13 pages and 3 references” and I was the guy who would ask “can I have 20 pages and 12 references?”. Most students were making their periods in sentences bigger as a trick to make it look like their papers were longer: I made my periods smaller to give myself more room to write. One day, I opened literally every paper relevant to my research on the Ebsco research database in a tab on Chrome. I read every one of those research papers.
In my statistics class, our teacher gave us the ability to use an Excel Spreadsheet to solve for the really challenging problems, but I preferred paper and pen, because I knew the answer would be 100% accurate if I worked it out myself and relied on pure math to find the right answer.
I ended up also with a minor in Biblical Studies, with a focus on exegetical Biblical text. I’d spent countless hours reading the Hebrew and Greek origins of words, pouring over the historical context so that I could draw the historical bridge, and would eventually map everything together to illustrate the connectedness of it all.
And today, I lead an engineering team of 35 people distributed in at least 12 countries. I’m the top-level director, responsible for estimating projects from $300k-$2M in size, ranging 3mo to 18mo in duration, and for teams ranging in size from 5-20 people. Our margins are razor thin, so if my projections are off by the slightest, our company could be devastated. Instead, in the last four years we’ve quadrupled revenue, increasing our team size from 15 to 70 people. The growth has been massive. But we’ve stayed profitable and debt free because of our attention to detail, the thoroughness of our research, and the follow through on commitment, of which I’m chiefly responsible.
For the free time I have outside of managing my team, I spend much of my time in spreadsheets creating forecasting models, and also doing research on emerging technology. On average, I’ve learned one new computer language every 3 months the last 6 years (when I had gotten my start in engineering, I had learned 6 languages in just two weeks).
The point I’m trying to make is that I am a research, math and science guy if you’ve ever met one. I trust in facts, not hypotheses; evidence, not narratives; logic, not feelings. If it weren’t for my faith in Jesus Christ, my faith would be wholly in math, science and logic. Thankfully, God had room for me in His family. My love of God, and faith in Him, however, doesn’t change anything about my love and appreciation for math and science. That’s who God made me at the core. I believe in the rigor of research, the reliability of math, and the soundness of logic and reason. Knowing God has simply positioned my trust in Him before human reason, and above reason when in conflict. But if it weren’t for God’s grace over me, you’d probably think I was Spock’s offspring or worse, even his father.
On My knee-jerk reaction was that these people were loonies. I did some research at the time, and was able to verify their claims that some vaccines had aborted baby tissue in them. That made me sick, and certainly made me for the first time ask the question, “what’s in vaccines?”. I had never asked that before. Not once. I just knew they were good. I researched a little more, wrestled with the topic of vaccines, and ended up deciding that when I had kids I’d look more into it with an open mind — but that by and large, most vaccines are still good.
That was a decade ago. The last few months, I began researching vaccines again. This time around, I’ve applied the same level of rigor that I’ve always applied to research, math, science, logic and reason. I’ve spent at least 100 hours in the last 1-2 months, and quite honestly, I’m just now starting to scratch the surface. There’s so much that I don’t yet know, so many sources and references I haven’t stored that I need to go back and save, and so much that I have yet to validate or invalidate.
But, from what I’ve learned so far, I’m convinced thatwe should at minimum be asking questions about vaccines. I’ve written my bonafides above so that you know in full faith and confidence, that I’m likely the most skeptical person you will meet when it comes to changing my opinion, especially on something as central as vaccines, for which in the last 26 years I have accepted as right and true without question. I’m a hardcore “INTJ” personality type: known for being unwilling to change, for always thinking I’m right, and for being out of touch with feeling and emotion. While God has tempered me with grace to love and care for those around me, my affinity for being persuaded by anything less than logic and reason (outside of faith) is exactly zero.
Below, I’ll share a high-level overview about why we should be concerned about some vaccines, and why,we should be engaged with our government to ensure that our kids and grandkids won’t grow up in a world where the government mandates vaccine injections. I’ll keep each of these relatively short and include resources below if you want to dig in to learn more.
A. HEALTH CONCERNS
1. VOLUME OF VACCINES
When I was born (1988), the recommended vaccine schedule included four vaccines:
Diphtheria, tetanus, & acellular pertussis
Inactivated poliovirus
Measles, mumps, rubella (MMR)
Haemophilus influenzae type b
Today, the vaccine schedule has tripled to fifteen vaccines:
Hepatitis B
Rotavirus
Diphtheria, tetanus, & acellular pertussis
Haemophilus influenzae type b
Pneumococcal conjugate
Inactivated poliovirus
Influenza (IIV) / Influenza (LAIV)
Measles, mumps, rubella (MMR)
Varicella
Hepatitis A
Tetanus, diphtheria, & acellular pertussis
Human papillomavirus
Meningococcal
Meningococcal B
Pneumococcal polysaccharide
2. VOLUME OF VACCINE DOSAGES
When I was born,the number of vaccine dosages was 15.
The number of vaccine dosages has tripled to 44.
3. VACCINE SCHEDULES
When I was born, the schedule for when to administer vaccines was less aggressive. The CDC at the time did not have an official schedule for when to administer the doses based on age of the baby. That changed in 1995.
Today, the vaccine schedule recommends 27 doses of vaccines prior to the age of 15mo, with 17 of those prior to 6mo old.
4. COMBINATION VACCINES
Some vaccines have been combined in high concentration doses. For example, Measles, Mumps and Rubella each had their own vaccine available. In the 70s-80s, these vaccines were combined into one highly concentrated vaccine, referred to as MMR. Many are concerned about injecting this high concentration of vaccine all at once into small, developing babies. Vaccine producers have taken the individual vaccines off the market and only offer the combination vaccine.
SUMMARY
In my personal research, I’ve seen an overwhelming number of stories of people’s babies who are otherwise healthy, engaged, and developing, but experience immediate seizure and disengagement upon receiving the MMR vaccine, resulting in autism. Similarly, there are an overwhelming number of people who have been paralyzed after receiving the Human papillomavirus vaccine. These are referred to as Vaccine Injuries, and these aren’t the only two vaccines that cause them.It’s challenging for parents with infants to prove that a vaccine caused an injury, because lawyers will often make the case that there’s no way to know that the vaccine caused autism since the baby is so young and still developing. I’ve scoured the web looking at many before and after narratives, with videos and pictures to boot, and there’s ample evidence that there is in fact a sudden and massive change in other-wise happy babies.
If that’s not enough though, given the Human papillomavirus vaccine is administered around 11-12 years old (or even as young as 9), it’s much more challenging for lawyers to make the case that an otherwise healthy 15 year old who became paralyzed after taking the vaccine wasn’t the cause of the vaccine. Here’s what’s most disturbing about the vaccines for HPV: the virus is only transmitted via sex, and especially via anal sex. The CDC recommends administering this vaccine automatically to all women — I should say, “adolescent girls” — between the ages of 11-12, and even as young as 9. Further, the virus is found in most cases to go away on it’s own, it’s rare that it results in the deadly condition of Cervical Cancer. On their page for the HPV Vaccine, the CDC sites that 12,000 women are diagnosedwith Cervical Cancer each year — but HPV isn’t the only cause of Cervical Cancer, it’s one of many.How many cases were a result of HPV? Even still, the number is massively low: 12,000 cases and 4,000 deaths. But, they recommend every young girl in America receive the vaccine — and there are many stories of parents whose daughters contracted Guillain-Barre Syndrome within 2 weeks of being vaccinated for HPV specifically with Gardasil. Gardasil happens to be the only vaccine available for HPV. At least three states (Rhode Island, Virginia, and District of Columbia) have passed legislation mandating children be vaccinated with Gardasil by 7th grade. Many more states have put forward legislation.Gardasil is one of the darling vaccines in the Merck Co. inventory, and in 2018 alone generated $3,000,000,000+ ($3B ) in revenue.
There’s such a high number of people who report vaccine injuries, that in 1988, the federal government and CDC stood up the National Vaccine Injury Compensation Program to deal with the mass number of cases reported. The Compensation Program offers payment only with a ‘no fault’ stipulation, as a means to silence people who have experienced vaccine injuries.Since 1988, $4,027,385,399.60 ($4B) has been disbursed to vaccine injury claims and another$216,791,324.93 ($200M) paid to legal fees for the United States Government providing lawyers to defend against these claims on behalf of vaccine producers.
In this post, I’m not going deep into theVaccine Injury data, although it’s quite voluminous. Instead, I thought I’d simply highlight that there’s been a very recent and rapid spike in the volume of vaccines, doses and acceleration of schedules, coupled with massive amount of injury claims being paid out to individuals. That’s enough to make me go, “hmm…”. If you are interested in stories from people who have experienced Vaccine Injury, check out the movie Vaxxed and Vaxxed 2.If it’s all just rubbish, it’ll be a good laugh for you. If it’s not, perhaps you’ll something.
Aborted baby fetal tissue samples from two babies (tissues referred to as MRC-5 and WI-38) are used in the production of at least four widely distributed vaccines (name of the vaccine manufactures who use the aborted fetal tissue referenced next to the vaccine name). Many object morally to using aborted baby tissue in vaccines. Some of these vaccines are mandated, which presents special challenges for those who morally object:
Hepatitis A vaccines [VAQTA/Merck, Havrix/GlaxoSmithKline, and part of Twinrix/GlaxoSmithKline]
Rubella vaccine [MERUVAX II/Merck, part of MMR II/Merck, and ProQuad/Merck]
Varicella (chickenpox) vaccine [Varivax/Merck, and part of ProQuad/Merck]
Zoster (shingles) vaccine [Zostavax/Merck]
These are just the vaccines produced through these two widely known strains of aborted fetal tissue. There are many more tissues from other aborted babies that are also used in widely administered vaccines (you can do your own googling on these!).
2. VACCINE APPROVAL RIGOR
Vaccines don’t go through the same rigor of testing that pharmaceutical drugs approved by the FDA go through.Specifically, vaccines don’t necessarily go through placebo studies.This means that when a new vaccine comes out, or if it’s been out for 50 years, scientists refuse to test the efficacy of the vaccine against the natural immunity of individuals’ who do not have the vaccine (nor of the side effect comparisons). Because of this, it is nearly impossible to link vaccine injuries to vaccines, because researchers refuse to test against placebos. So, when a new vaccine comes out, if there’s an increase in autism because of the vaccine, you wouldn’t know that necessarily because everyone would have received the vaccine, so it looks like the entire population just had an uptick in autism (for other nefarious reasons). This makes it nearly impossible to hold accountable any vaccine producer against the side effects and injuries their vaccines produce. It also makes it harder to trust the vaccines.
These scientists cite the reason for their objection to placebo studies as it being “unethical” to not give their wonderful mana-from-heaven vaccine to the children of the world. After all, their vaccine saves lives. So, we should just trust that the vaccine saves lives and not question the integrity of their work. After all, they are scientists. Scientists never make mistakes.
Some have challenged scientists on this notion, in that there are many parents who would be willing to not give a vaccine to their children, because they specifically do not want the vaccine. The objection from scientists in this case is that the parents are pre-disposed to a bias, and they cannot trust the results of the test because the parent will add confirmation bias to the results.
3. VACCINE TRADEOFF VALUE
The diseases that many of the newer vaccines on the vaccine schedule treat are low in number of affected cases and mortality rate.For example, there’s a few vaccines that treat diseases that might affect 50,000 of the population in the United States (of 323M) with less than 200 deaths. Does it really make sense to vaccinate 323M people for something that is this rare? As we see the vaccine schedule growing so large, you have to wonder if at some point if it’s worth the risk of all those chemicals in our body to protect ourselves against infections and diseases for which we have an incredibly low chance of getting, and even lower chance of dying from.
4. VACCINE MANDATES
Vaccines have become increasingly mandated by state and local governments. In most states, a child cannot attend public and many private schools without providing evidence that they have received the minimum required vaccines. In many states, a parent not providing vaccines can be constituted as Medical Neglect meaning that a parent can lose rights to their children and even be fined and serve jail time for choosing to not vaccinate their children.
5. VACCINE PRODUCERS’ LACK OF FINANCIAL/LEGAL LIABILITY FOR VACCINE INJURIES
Earlier, I mentioned theVaccine Injury Compensation Program established in 1988. Interestingly, this program offers 100% protection to Vaccine producers from any lawsuits from vaccine injuries (including mandated vaccines),and instead,holds the United States government liable financially but not criminally for any injury (thus, no one can be held criminally liable for vaccine injuries). I mentioned earlier that this is a “no fault” program, meaning those who file must maintain the explicit understanding and make clear that they do not hold the Vaccine producers at fault for their claim of injury (this is the only way they could be eligible to receive financial recompense — and of course, if a vaccine really did cause autism, it’s highly likely they would be dependent on the financial recompense to help offset the challenge of raising an autistic child).
The logic for absolving vaccine producers from having any culpability whatsoever is that in the 80s, there were so many people filing suits against vaccine companies, that these vaccine producers were getting buried in legal fees and payouts. They couldn’t afford to stay in business, producing more (questionable) vaccines, with all the claims of injuries. The United States decided to bail them out permanently — offering amnesty, hall pass, whatever you want to call it — so that they never have to face the consequence of any of their actions. Margaret Sanger published “My Way To Peace”a pretty dangerous recipe for mistakes. We’ve removed accountability on both book-ends of the process (pre-release-testing and post-administration-audits).
6. VACCINE AS POPULATION CONTROL
The Bill and Melinda Gates Foundation is now the #1 Contributor to the WHO (was second to the United States until Trump pulled back funding this year). In addition, The Bill and Melinda Gates Foundation has invested $11B in philanthropic efforts, with most of that going towards vaccine production, and a large chunk of that focused on vaccine production in Africa and Southeast Asia.
Massive research has been performed by the WHO on human chorionic gonadotropin (hCG) vaccines (informally known as sterilization vaccines). Researchers have discovered hCG presence in vaccines administered to people in developing countries (specifically, on tetanus vaccines). More concerning, women have been found to have been sterilized through the administration of vaccines (like the tetanus vaccine) in those developing countries.
Some researchers and philanthropologists (especially Bill Gates) have theorized that CO2 emmissions from people is one of the most damaging contributors to Climate Change, and have set out on a mission to solve the problem. Most notably, these researchers (led by Bill Gates and the WHO) have deemed Africa and Southeast Asia as the most responsible countries for contributing to overpopulation by 2050 (and thus, climate change), and have committed to reducing the population curve in these countries — specifically through contraceptive “options”.
In 2010, Bill Gates led a TED talk describing the relationship between increased health, vaccines and decreased population. Years later, he clarified his intention in this relationship, describing that he believes when people are healthier they’ll choose to have less kids.
Then, in 2015, Bill Gates hosted a convention in Berlin, Germany with worldwide leaders (funders, academia, regulatory agencies, non-governmental organizations, vaccine manufacturers, and Ministries of Health from Africa and Asia) focused on increasing vaccine administration in developing countries, specifically Southeast Asia and Africa. The convention was explicitly focused on maternal immunization (MI) against influenza, pertussis, and tetanus. In lay-mens terms, the convention was focused on how to administer influenza, pertussis and tetanus vaccines to pregnant women in Southeast Asia and Africa. The convention cited that the #1 challenge to administering the vaccine to these pregnant women was in fact resistance and objection by those pregnant women. The convention goes on to demonstrate that not enough evidence is yet available to demonstrate the efficacy or safety of the MI program, but after they administer to enough women and collect evidence (hopefully supporting their hypotheses), they will be able to use this evidence to generate greater demand from more individuals in those regions. To offset the challenge of overcoming objection from the pregnant women, the convention leaders asserted that they will need to leverage family members, tribal elders and religious leaders to critically influence community acceptance for the MI program to not just the pregnant women, but the entire community.
This isn’t the first time Bill Gates has heard of this technique of leveraging a woman’s community to propagate acceptance of immunization. Bill Gates’ father, Bill Gates Senior, served on local and national boards for Planned Parenthood leading up to Roe v. Wade. Many attribute his efforts and advocacy within Planned Parenthood as a boon for the pro-choice “victory” out of Roe v. Wade. When asked how he came to be passionate about reproductive issues as a philanthropic effort, Bill Gates references the efforts of his mom and dad, and specifically referenced the work they did in Planned Parenthood leading up to Roe v. Wade. Margaret Sanger, founder of Planned Parenthood,wrote a letter in 1939 to Clarence Gambel stating the following,“The most successful educational approach to the Negro is through a religious appeal…We don’t want the word to get out that we want to exterminate the Negro population, and the minister is the man who can straighten out that idea if it ever occurs to any of their more rebellious members.”So the Bill and Melinda Gates foundation, 76 years later, takes a pretty similar approach in Africa for the MI program,using tetanus, which has been known to be a a disguised carrier for hCG sterilization.
But this isn’t the only thing concerning about Bill Gates’ ties to Planned Parenthood. Margaret Sanger started Planned Parenthood a few different times under different names, and even retreated to Germany in the midst of WWII for safe haven from the United States government for her practicing of eugenics on African Americans. Specifically, her goal was to limit population and reproduction of African Americans. The third time she started the organization, it was thus named Planned Parenthood. And her legacy lives today.79% of all Planned Parenthood facilities are within walking distance of African American communities. According to a study by the CDC in 2015, since 1969, Black women have the highest abortion rate of any other race, consisting of 36% of all abortions in the United States (African American population is ~12%). Let me say that another way: 12% of the population is responsible for 36% of all abortions.
In 1932, Margaret Sangerpublished “My Way To Peace”, postulatingtoCongress to “direct and control the population through Birth rates and immigration”.
Three of her main objectives were as follows:
(d) apply a stern and rigid policy of sterilization, and segregation to that grade of population whose progeny is already tainted or whose inheritance is such that objectionable traits may be transmitted to offspring.
(e) to insure the country against future burdens of maintenance for numerous offspring as may be born of feeble-minded parents,the government would pension all persons with transmissible disease who voluntarily consent to sterilization.
(f) thewhole dysgenic population would have its choice of segregation or sterilization.
Margaret Sangerpublished “My Way To Peace”
That Bill Gates derives his philanthropic loins from his father’s service in Planned Parenthood, during which time he helped Planned Parenthood win Roe v Wade, which has effectively resulted in ~62M abortions, 19M of which from African Americans — and that Bill Gates has invested $11B towards producing vaccines in Africa and Southeast Asia for the purpose of population control, and that he would focus on using the tetanus shot as one of three primary vaccines (which has been proven in developing countries to contain hCG sterilization) in specifically African pregnant women — is highly questionable and concerning.
People ask me: “why do you share this kind of knowledge” and I’ll tell you why. If there’s the smallest chance that there exists a man who is intentionally sterilizing women in developing countries against their knowledge and will, I believe we should fight against such an oppressor in prayer and otherwise. I believe that falls in the category of James 1:27, to fight for widows and orphans — to fight for the least of these.
The United States has paid out $4B in vaccine injury claims and $200M in legal fees since 1988 on behalf of vaccine producers. Where does Uncle Sam get his money? Taxpayers, not vaccine producers, pay the price for vaccine injuries.
2. BIG PHARMA PROFITEERING
Meanwhile, vaccine manufactures are on schedule to earn $60,000,000,000 ($60B) in 2020 alone. Since they aren’t bogged down with dealing with pesky lawsuits, they can focus on generating more vaccines to add to the schedule.
Let’s take a quick look at how Coronavirus has affected stocks for seven of the biggest Vaccine producers.
Three of the biggest 10 vaccine producers are Novavax, Inovio, and Vir Biotechnology. Since Coronavirus, these three companies’ stock has skyrocketed:
Wow! If you look closely, you’ll see these companies experience a massive spike in growth around January-March. It’s quite natural that we would see vaccine stock markets increase due to COVID. But what’s interesting is not all vaccine company stock markets experienced this spike. In fact, these three are the outliers. What do these three share in common?They are all backed by Bill Gatesfor a collective $244M.
Here’s what the stocks look like for the #1, #2, #3 and #4 revenue producing vaccine producers:
The common thread we see here is a big dip. None of them expected Coronavirus, they all experienced massive disruption in their business and are now recovering.Why did they experience a dip? Logically: people stopped going to hospitals to get their regular vaccines and sales plummeted overnight.
If you look at the stock for the firms Bill Gates has heavily invested in, you see the inverse: there’s actually a spike. As if they were ready for Coronavirus to hit. Why is this?
Speaking of, Bill Gates in 2015 predicted this pandemic, nearly to the tee: A flu-based pandemic by around 2020 flu-based pandemic, of the weight and gravity of the 1918 Spanish Flu. He’s been leveraging this prediction to convince people of the need for a worldwide vaccine. He’s specifically been at work to ensure vaccine distribution is ready to go in Africa and Southeast Asia. We also see a massive acceleration in his financial investments in vaccine organizations starting in 2015. This overlaps well with the Berlin convention in 2015 where he asserted the biggest challenge with vaccinating pregnant women is their objection to being vaccinated.
Be on the lookout for any research that suggests pregnant women are especially at risk of Coronavirus, it wouldn’t surprise me if the CDC and WHO recommend a pregnancy specific vaccines for Cornavirus in the next year. It wouldn’t surprise me if Bill Gates graciously offers to donate another $10B to getting this vaccine to Africa and Southeast Asia.
He sure is great at predicting the future — and many still believe his intentions are pure. What do you think?
Vaccines wouldn’t be a concern of mine if they weren’t mandatory in the United States and if they weren’t seemingly being used to propitiate sterilization of ethnic groups in developing countries.
I’d like to reiterate one thing in all of this: this is just scratching the surface. The amount of data I’ve combed through, the evidence, hours-and-hours of testimony from individuals — it’s overwhelming. I’ve included only references in here which are either neutral or pro-vaccine. I’ve specifically not included references to data in here that is clearly anti-vaccine. I’ve done this on purpose so that you may look at the data that is skewed in favor of pro-vaccines and make a determination for yourself if you have any concerns based on the best case scenarios.
Personally, in reviewing the data, I’m alarmed by the interconnectedness of what we are seeing. Coupled with the increased censorship from Facebook, the WHO, the CDC and Google, who all appear to be in lock-step, it’s hard to know what to do with all of this information. I’ve often debated internally: “should I just be silent about this?” and “of what value does this provide?”
But, I’m continually convicted of the following nine beliefs, and I cannot shake these nor be silent:
I’m concerned by the harmfulness of many vaccines
I’m concerned by the lack of good science behind testing vaccines
I’m concerned by the lack of accountability beholden to vaccine producers
I’m concerned by any group of people who would attempt to sterilize any person or group of peoples
I’m increasingly concerned by the calls for a worldwide vaccine, especially one that is mandated
I feel morally compelled to share these convictions with others, so they themselves can decide if they want to subject themselves and their families to vaccines
I feel morally compelled to pray often for our government leaders to be surrounded by God-fearing, righteous men and women, and to be removed from the sphere of influence of anyone who does not daily submit themselves before the Lord
I feel civilly compelled to figure out how to create awareness in our communities so that we can elect officials who are committed to tackling these concerns, and also advocate to already elected officials to do something about it; and to not just stop in our own communities, but to change our laws so that we are better able to hold accountable vaccine producers — and keep big money out of influencing what we do with vaccines, and how we do it
I feel morally obligated to figure out what my role is in helping prevent the oppression of widows and orphans in developing countries from rich and powerful men who have clearly stated their objective to reduce population in those developing countries
To be clear, I have no quarrel with anyone who is pro-vaccine. In fact, when produced with upmost ethical standards, it’s quite sensible to me that people would be highly interested in vaccines. However, I also seek to preserve independent medical freedom for individuals to weigh both the science and the testimonies of those who have had vaccines — and to decide what the best course of action is for them and their families. On a personal level, I feel responsible for the safety of my own family.
One indication that the government is not in tune with safe vaccine protocols is that they still maintain a “no fault” policy on vaccines, and refer only to vaccine “allergic reactions” without acknowledging the many diseases, illnesses and deaths they do clearly cause. Despite this, it’s clear to me that there are people out there who think it best for the government to decide what is safest — that we as individuals should not maintain that freedom. I am unequivocally against these people and will oppose them at every measure
Kakistocracy: noun, government by the worst persons; a form of government in which the worst persons are in power.
The old saying goes that even a blind squirrel finds a nut occasionally. So you might think that during a 50-year political career, the odds would dictate that Joe Biden would, once in a blue moon, make a correct decision — just based on the odds. But you’d be mistaken. Biden has stumbled and bumbled from one disastrous decision to the next. Disastrous, that is, for America. Biden himself has prospered handsomely in spite of his glaring incompetence and corruption.
Biden’s long Senate career was based on being the credit card companies’ man in Washington. While crowing endlessly about the working class being “his people,” Biden sponsored bills allowing bank issuers to charge egregious interest rates and to make it harder for working men to escape the credit trap through bankruptcy.
When Biden chaired the Senate Judiciary Committee, he turned the confirmation of Clarence Thomas into a political smear campaign that descended into a degenerate three-ring circus. In his first campaign for president, he failed to garner a single percentage point before having to withdraw when confronted with his past lies and blatant plagiarism. He literally stole a speech detailing a British politician’s life story. He ran again in 2008 but again failed to reach even one percent of the vote.
When Barack Obama took him off the primary trash heap to make him vice president, Biden first made a hash out of the 2009 American Recovery and Reinvestment Act, wasting hundreds of billions on boondoggles and giveaways to Democrat cronies. Little of the recovery billions was spent on anything useful to America. Biden went on to manage our relations with China and Ukraine, pocketing untold millions for himself and his family by selling out America’s security interests.
By the time he ran for president again in 2020 he was a spent husk of his former corrupt and incompetent self, delivering asinine performances in the Iowa caucus and New Hampshire primary. When the Democrat establishment propped him up to once again stop Bernie Sanders, Biden was set up for the strangest presidential campaign in modern history. While Donald Trump barnstormed the nation with packed, enthusiastic rallies, Biden cowered in his basement, occasionally venturing out to speak with a few dozen voters sitting in circles drawn on the floor.
For his vice presidential pick, he chose — if you can believe it — an even more buffoonish candidate than himself.
Had it not been for Mark Zuckerberg buying and staffing government election offices in swing states, and the media and Big Tech’s censorship of the Biden family’s corruption, Biden would now be enjoying his dotage in Delaware, creeping on unsuspecting children with yarns of Corn Pop and South African arrests.
Instead, the man with one of the most astonishing records of abject failure in Washington was installed in the White House, and he has remained true to form. As one of a hundred senators and then as vice president, there was a limit to how much damage he could do. But as president, the shackles have been removed.
His first agenda item was to throttle our oil and gas sector, offshoring tens of thousands of good paying jobs to Russia and the Middle East — along with our energy independence. He threw open our southern border and encouraged virtually unlimited illegal immigration — during a global pandemic.
Biden’s “defund the police” rhetoric delivered us soaring violent crime in Democrat-run cities, while he sicced federal law enforcement on parents who object too strenuously to their children being indoctrinated with anti-White racism and LGBTQIA+ ideology.
It can truly be said that as president, Biden’s record of failure remains unblemished.
But now comes what may be the capstone on Biden’s long history of buffoonery and corruption. In Ukraine, we have an armed conflict that threatens to plunge the world into an economic depression and raises the specter of nuclear war. Not only did Biden set the stage for this calamity when, as vice president, he was in charge of Ukraine policy and led Kiev to believe that NATO membership was in Ukraine’s future, but on the eve of the Russian invasion, he refused to admit that it was not. Then Biden all but admitted to Vladimir Putin — on live TV, no less — that NATO would not defend Ukraine if Russia chose to invade.
In the aftermath of Russia’s invasion, Biden and his administration have crafted sanctions that seem almost designed to boomerang on America’s and Europe’s fragile post-pandemic economies, while forcing Russia into a deeper alliance with China.
With the U.S. over $31 trillion in debt, Biden seems totally oblivious to the perilous position of the U.S. dollar as the world’s reserve currency and the consequences should that privileged position end.
Economists predict that food and gasoline will cost the average U.S. household an additional $3,000 this year, and inflation threatens to push millions of lower-middle income-earners into abject poverty.
And bumbling, corrupt Joe Biden isn’t yet halfway through his first — and please God, last — term.
The Trailblazing Patriot 