Rest assured, this is just the tip of the iceberg……there’s more
FOIA Judicial Watch has uncovered a substantial amount of information regarding COVID-19 issues:
In October 2020, Judicial Watch received FDA records that detailed pressure for COVID-19 vaccine booster approval and use.
NIH records revealed an FBI “inquiry” into the NIH’s controversial bat coronavirus grant tied to the Wuhan Institute of Virology. The records also show National Institute of Allergy and Infectious Diseases (NIAID) officials were concerned about “gain-of-function” research in China’s Wuhan Institute of Virology in 2016. The Fauci agency was also concerned about EcoHealth Alliance’s lack of compliance with reporting rules and use of gain-of-function research in the NIH-funded research involving bat coronaviruses in Wuhan, China.
HHS records revealed that from 2014 to 2019, $826,277 was given to the Wuhan Institute of Virology for bat coronavirus research by the NIAID.
NIAID records showed that it gave nine China-related grants to EcoHealth Alliance to research coronavirus emergence in bats and was the NIH’s top issuer of grants to the Wuhan lab itself. The records also included an email from the vice director of the Wuhan Lab asking an NIH official for help finding disinfectants for decontamination of airtight suits and indoor surfaces.
HHS records included an “urgent for Dr. Fauci ” email chain, citing ties between the Wuhan lab and the taxpayer-funded EcoHealth Alliance. The government emails also reported that the foundation of U.S. billionaire Bill Gates worked closely with the Chinese government to pave the way for Chinese-produced medications to be sold outside China and help “raise China’s voice of governance by placing representatives from China on important international counsels as high level commitment from China.”
HHS records included a grant application for research involving the coronavirus that appears to describe “gain-of-function” research involving RNA extractions from bats, experiments on viruses, attempts to develop a chimeric virus and efforts to genetically manipulate the full-length bat SARSr-CoV WIV1 strain molecular clone.
HHS records showed the State Department and NIAID knew immediately in January 2020 that China was withholding COVID data, which was hindering risk assessment and response by public health officials.
University of Texas Medical Branch (UTMB) records show the former director of the Galveston National Laboratory at the University of Texas Medical Branch (UTMB), Dr. James W. Le Duc warned Chinese researchers at the Wuhan Institute of Virology of potential investigations into the COVID issue by Congress.
HHS records regarding biodistribution studies and related data for the COVID-19 vaccines show a key component of the vaccines developed by Pfizer/BioNTech, lipid nanoparticles (LNPs), were found outside the injection site, mainly the liver, adrenal glands, spleen and ovaries of test animals, eight to 48 hours after injection.
Records from the Federal Select Agent Program (FSAP) reveal safety lapses and violations at U.S. biosafety laboratories that conduct research on dangerous agents and toxins.
HHS records include emails between National Institutes of Health (NIH) then-Director Francis Collins and Anthony Fauci, the director of National Institute of Allergy and Infectious Diseases (NIAID), about hydroxychloroquine and COVID-19.
HHS records show that NIH officials tailored confidentiality forms to China’s terms and that the World Health Organization (WHO) conducted an unreleased, “strictly confidential” COVID-19 epidemiological analysis in January 2020.
Fauci emails include his approval of a press release supportive of China’s response to the 2019 novel coronavirus.
A “Pharmacokinetics Written Summary” marked “Confidential,” indicates that the information it contains is related to the mRNA-1273 (Moderna vaccine) strain, however, much of the data comes from work with mRNA-1647. The study states:
The results of a biodistribution study of mRNA-1647 support the development of mRNA-1273.
The biodistribution of mRNA-1647 was evaluated in a non-Good Laboratory Practice (GLP), single-dose, intramuscular (IM) injection study in Sprague Dawley rats…. mRNAs that are within an LNP of the same composition (e.g., mRNA-1273 and mRNA-1647) are expected to distribute similarly.
According to PubMed.gov, “Pharmacokinetics studies are performed to clarify the absorption, distribution, metabolism, and excretion of drug candidates…[and] are required for establishing the efficacy and safety in humans.”)
In one appendix to the study, a “clarification” was issued in the toxicokinetic report regarding the half-life of mRNA injected into the rats, noting: “The average value of terminal half-life for the muscle (i.e. injection site) in Sections 4.2 and 5 of the toxicokinetic report should be read 14.9 [hours] instead of 8.39 [hours] based on the results of the toxicokinetic evaluation.”
The study further notes that the wording of the conclusion was modified to read, “The half-life … of mRNA-1647 was reliably estimated in muscle (site of injection), proximal popliteal and axillary distal lymph nodes, and spleen with average values for all construct t½ [half-life] of 14.9 8.39, 34.8, 31.1 and 63.0 hours, respectively.” [Emphasis in original]
Another appendix, titled “Summary Mean (±SE) mRNA-1647 Pharmacokinetic Parameters in Sprague-Dawley Rat in Plasma and Tissues Following 100μg Intramuscular Injection Administration of mRNA-1647 on Day 1,” reveals that, in addition to distributing to the muscle site, lymph nodes and spleen, the mRNA particles also distributed to the bone marrow, brain, eyes, heart, liver, lungs, stomach and testes.
A separate studyindicates that the mRNA-1647 particles injected into rats were “observed in muscle (i.e. site of injection), followed by proximal (popliteal) lymph nodes, axillary lymph nodes and spleen, suggesting the mRNA-1647 distribution to the circulation by lymph flow.” (The mRNA was delivered via “lipid nanoparticle dispersion.”)
“These previously hidden records about the COVID-19 vaccine safety and efficacy studies raise a number of disturbing questions,” said Judicial Watch President Tom Fitton. “The fact that it has taken a federal lawsuit to get access to this material is yet another scandal.”
Through this investigation of pediatric vaccine safety, the following findings are made:
1. Mercury is hazardous to humans. Its use in medicinal products is undesirable, unnecessary and should be minimized or eliminated entirely.
2. For decades, ethylmercury was used extensively in medical products ranging from vaccines to topical ointments as preservative and an anti-bacteriological agent.
3. Manufacturers of vaccines and thimerosal, (an ethyl-mercury compound used in vaccines), have never conducted adequate testing on the safety of thimerosal. The FDA has never required manufacturers to conduct adequate safety testing on thimerosal and ethyl-mercury compounds.
4. Studies and papers documenting the hyperallergenicity and toxicity of thimerosal (ethylmercury) have existed for decades.
5. Autism in the United States has grown at epidemic proportions during the last decade. By some estimates the number of autistic children in the United States is growing between 10 and 17 percent per year. The medical community has been unable to determine the underlying cause(s) of this explosive growth.
6. At the same time that the incidence of autism was growing, the number of childhood vaccines containing thimerosal was growing, increasing the amount of ethyl mercury to which infants were exposed threefold.
7. A growing number of scientists and researchers believe that a relationship between the increase in neuro-developmental disorders of autism, attention deficit hyperactive disorder, and speech or language delay, and the increased use of thimerosal in vaccines is plausible and deserves more scrutiny. In 2001, the Institute of Medicine determined that such a relationship is biologically plausible, but that not enough evidence exists to support or reject this hypothesis.
8. The FDA acted too slowly to remove ethylmercury from over-the-counter products like topical ointments and skin creams. Although an advisory committee determined that ethylmercury was unsafe in these products in 1980, a rule requiring its removal was not finalized until 1998.
9. The FDA and the CDC failed in their duty to be vigilant as new vaccines containing thimerosal were approved and added to the immunization schedule. When the Hepatitis B and Haemophilus Influenzae Type b vaccines were added to the recommended schedule of childhood immunizations, the cumulative amount of ethylmercury to which children were exposed nearly tripled.
10. The amount of ethylmercury to which children were exposed through vaccines prior to the 1999 announcement exceeded two safety thresholds established by the Federal government for a closely related substance–methylmercury.
While the Federal Government has established no safety threshold for ethylmercury, experts agree that the methyl mercury guidelines are a good substitute. Federal health officials have conceded that the amount of thimerosal in vaccines exceeded the EPA threshold of 0.1 micrograms per kilogram of bodyweight. In fact, the amount of mercury in one dose of DTaP or Hepatitis B vaccines (25 micrograms each) exceeded this threshold many times over. Federal health officials have not conceded that this amount of thimerosal in vaccines exceeded the FDA’s more relaxed threshold of 0.4 micrograms per kilogram of body weight. In most cases,however, it clearly did.
11. The actions taken by the HHS to remove thimerosal from vaccines in 1999 were not sufficiently aggressive. As a result, thimerosal remained in some vaccines for an additional two years.
12. The CDC’s failure to state a preference for thimerosal- free vaccines in 2000 and again in 2001 was an abdication of their responsibility. As a result, many children received vaccines containing thimerosal when thimerosal-free alternatives were available.
13. The Influenza vaccine appears to be the sole remaining vaccine given to children in the United States on a regular basis that contains thimerosal. Two formulations recommended for children six months of age or older continue to contain trace amounts of thimerosal. Thimerosal should be removed from these vaccines. No amount of mercury is appropriate in any childhood vaccine.
14. The CDC in general and the National Immunization Program in particular are conflicted in their duties to monitor the safety of vaccines, while also charged with the responsibility of purchasing vaccines for resale as well as promoting increased immunization rates.
15. There is inadequate research regarding ethyl-mercury neurotoxicity and nephrotoxicity.
16. There is inadequate research regarding the relationship between autism and the use of mercury-containing vaccines.
17. To date, studies conducted or funded by the CDC that purportedly dispute any correlation between autism and vaccine injury have been of poor design, under-powered, and fatally flawed. The CDC’s rush to support and promote such research is reflective of a philosophical conflict in looking fairly at emerging theories and clinical data related to adverse reactions from vaccinations.
One study that compared the toxicology of ethyl and methyl-mercury was published in 1985 in the Archives of Toxicology, written by researchers from the Toxicology Unit of the Medical Research Council of England. The researchers exposed rats to ethyl and methyl-mercury to “compare total and inorganic mercury concentrations in selected tissues, including the brain, after the daily administration of methyl or ethyl-mercury and to relate these findings to damage in the brain and kidneys.” This study found that both ethyl and methyl-mercury caused damage to the brains and the kidneys. It also found that male and female rats were affected differently: “It has been well documented that one of the first toxic effects of methylmercury in rats is depressed weight gain or even weight loss . . . based on this criteria, ethyl-mercury proved to be more toxic than methylmercury . . . in both sexes . . . the concentration of total mercury (the sum of organic and inorganic mercury) and organic mercury was consistently higher in the blood of ethylmercury-treated rats . . . both alkymercurials damaged the dorsal root ganglia and 9.6 mg Hg/kg/day ethylmercury caused more damage than 8.0 mg Hg/kg/day methylmercury. Ethylmercury was more renotoxic than methyl-mercury . . . tubular dilation was frequently present . . . in kidneys . . . both damage and mercury deposits were more widely spread in ethylmercury-treated rats.”
While there is frequent reference to the paucity of science in understanding the harm that ethyl-mercury can do, there is more understanding in the scientific community than government officials have shared with the Committee.
The mercury amalgams in your mouth, the so-called silver fillings, contain 48 to 50 percent of elemental mercury.
These fillings continuously emit mercury vapor, which will go to the brain and is converted to mercuric mercury . . .
Certain fish contain methylmercury; again, very rapidly taken up from the GI tract, transported quickly to the brain, and converted very slowly to mercuric mercury . . . thimerosal, which again will be taken up by the brain and quickly converted to mercuric mercury–all three forms are neurotoxic.
“By neurotoxic, we mean it will damage nerves and it will damage brain tissues.”
“Let me just say as a final statement that there is no need to have thimerosal in a vaccine.”
In making a presentation to the Institute of Medicine’s Immunization Safety Review Committee, in July 2001, the former Director of the Environmental Toxicology Program at the National Institutes of Health, Dr. George Lucier, proffered the following conclusions:
Ethyl-mercury is a neurotoxin.
Infants may be more susceptible than adults.
Ethyl-mercury should be considered equipotent to methyl-mercury as a developmental neurotoxin. This conclusion is clearly public health protective.
Ethyl-mercury exposure from vaccines (added to dietary exposures to methylmercury) probably caused neurotoxic responses (likely subtle) in some children.
While the debate over whether ethyl or methylmercury is more toxic will probably not be resolved in the near future, a consensus appears to be emerging that exposure to these different types of mercury cannot be considered in isolation.
Rather, witnesses before the Committee stressed that in determining safe levels of mercury exposure, the cumulative level of exposure to all types of mercury must be considered.
Dr. Jeffrey Bradstreet made the following observation at the
July 19, 2002 hearing:
“More concerning to me in the Institute’s treatment of mercury problems, was the almost complete absence of regard for compounding effect of thimerosal on preexisting mercury
levels. The NHANES Study from the CDC had already established that perhaps one in ten children is born to mothers with elevated mercury burden.
The Committee repeatedly heard from government officials that merely exceeding the guideline was not cause for concern. One Merck official, in teaching a Grand Rounds session to staff in November of 1999, postulated that the minimum risk level would need to be multiplied by ten to reach a level at which harm would be expected through exposure. Dr. Roberta McKee of Merck wrote:
“A number of environmental and public health agencies have set a Minimum Risk Level (MRL) for toxic substances. An MRL for ingestion is conceptually equivalent to the Reference Dose of the US Environmental Protection Agency, the Acceptable Daily Intake of the US FDA, and the Tolerable Daily Intake of the WHO. Any exposure to the substance below the MRL is assured to be safe, while exposure to ten times the MRL is assumed to place one at risk of overdose. Exposure at or near the MRL is assumed to be safe but should trigger deliberate and careful review.”
Based on Dr. McKee’s explanation, many babies were exposed to levels of mercury that “placed one at risk of overdose,” and were exposed to amounts well over ten times the EPA’s scientifically validated reference dose. For example, at a recent Committee hearing, Chairman Dan Burton (R-IN) discussed his own family’s experience with vaccine injuries:
“My grandson received vaccines for nine different diseases in one day. He may have been exposed to 62.5 micrograms of mercury in one day through his vaccines. According to his weight, the maximum safe level of mercury he should have been exposed to in one day is 1.5 micrograms, so that is 41 times the amount at which harm can be caused.”
According to the analysis of Dr. McKee, based on the methyl-mercury ingestion guidelines, the Chairman’s grandson would have exceeded the “ten times the MRL” and therefore was placed “at risk of overdose.” In fact, with a 62.5 microgram exposure alone, the EPA, ATSDR, and FDA levels would have been exceeded by 10 times. Because the FDA chose not to recall thimerosal-containing vaccines in 1999, in addition to all of those already injured, 8,000 children a day continued to be placed “at risk for overdose” for at least an additional two years.
It should also be noted that none of the Federal guidelines on mercury exposure have been included specific provisions for safe exposure limits for infants and children. It is widely accepted that infants and young children would be five times more sensitive to the toxic effect of mercury or other neurotoxins than adults. “Exposures early in life are reasonably of greater health concern . . . because of greater brain organ susceptibility.” The FDA has conceded in recent years that many children received doses of ethylmercury through their vaccinations that exceeded the EPA’s minimal risk level for methylmercury.
However, it is also clear that many infants received doses of ethyl-mercury that exceeded the FDA’s higher threshold.
Whatever you may currently think about the SARS-CoV-2 vaccines, it is a fact that more than 5.41 billion people worldwide have received a dose of some type of COVID-19 vaccine, equal to about 70.5 percent of the world population. In the United States as of October 17, 2022, 494.74 million “initial protocol doses” of SARS-CoV-2 vaccine have been administered, together with 138.16 million “booster” doses. 265.59 million US residents have received at least one dose, and 226.59 million have completed the initial vaccination protocol (see this link), out of a total population of 335.49 million (67.5%). In terms of the logistics of development, manufacturing and deployment of a novel injectable biologic product, this is undeniably a major achievement.
Of the SARS-CoV-2 mRNA vaccine doses administered in the United States as of October 19, 2022:
375.64M doses of Pfizer/Bio-N-Tech 237.61 doses of Moderna
Total U.S. of 613.25M mRNA vaccine doses administered.
In the European Union, the corresponding numbers are:
641.89M doses of Pfizer/Bio-N-Tech 153.16M doses of Moderna
EU total of 795.05M mRNA vaccine doses administered
Grand Total of 1 Billion
408.3 million doses of mRNA vaccines in these two regions.All this involves a novel technology, product and large scale manufacturing process which was created, passed non-clinical and clinical development and was massively manufactured, distributed and globally deployed in less than three years.
At a meeting of the Special Committee of the European Union Parliament held on 11 October 2022 to discuss the findings regarding COVID-19 pandemic and recommendations for the future, a Pfizer executive confirmed that the vaccine had never been tested for its ability to prevent the transmission of SARS-CoV-2 virus before being put on the market. Data emerging since the introduction of the vaccine indicates that it is in fact unable to do so, thereby refuting the claim that the COVID-19 Passports provide any guarantee of protection. In other words, although governments throughout the world employed a wide range of propaganda and censorship methods to promote these products as both safe and effective at stopping the spread of SARS-CoV-2 infection, there were no studies performed prior to this distribution which even tested how well the products would prevent the spread of COVID-19 disease. It is not an exaggeration to state that this massive deployment has been the largest clinical experiment performed on human beings in the history of the world.
All of the mRNA vaccine doses administered in the United States (to both citizens and military personnel) have been provided under “Emergency Use Authorization” (EUA), which is to say that although the FDA has licensed the Pfizer/Bio-N-Tech and Moderna vaccines for some age cohorts, the firms have elected to not manufacture, distribute, or market these licensed products in the United States. The reason for this is not clear, but appears to relate to both liability issues as well as conditions placed by the FDA involving additional clinical studies, safety monitoring (pharmacovigilance) and product disclosures once the products begin to be marketed.
From the standpoint of the vaccine manufacturers, EUA is a preferred pathway for marketing their products. A single purchaser (the US Government) provides complete liability indemnification, a guaranteed market with very little oversight, and manages both the distribution and marketing. In the case of all unlicensed products, the manufacturers are prohibited from marketing them, but under EUA the US Government has been doing this for them, and has been acting in coordination with corporate media, social media, and large technology firms to suppress any discussion of risks or limitations of the products. From the standpoint of the vaccine manufacturers, this is all profit and no risk; a perfect business model. Why would they ever want to consider taking up the burden of actually producing and marketing the licensed version of these products?
EUA is a process defined by US federal law (21 U.S. Code § 360bbb–3 – Authorization for medical products for use in emergencies) which in the case of these mRNA-based products involves biological products which are not approved, licensed, or cleared for commercial distribution. Specifically, the statute authorizes “the introduction into interstate commerce, during the effective period of a declaration under subsection (b), of a drug, device, or biological product intended for use in an actual or potential emergency.” Continued “Emergency Use Authorization” of these vaccines requires “a determination by the Secretary of Homeland Security that there is a domestic emergency, or a significant potential for a domestic emergency, involving a heightened risk of attack with a biological, chemical, radiological, or nuclear agent or agents”. Once the domestic emergency has passed (ergo “a determination by the Secretary, in consultation as appropriate with the Secretary of Homeland Security or the Secretary of Defense, that the circumstances described in paragraph (1) have ceased to exist”), “A declaration under this subsection shall terminate”. In other words, when there is no longer an emergency, the “Emergency Use Authorization” for the product will cease, and the vaccine products will return to their status as not approved, licensed, or cleared for commercial distribution. These products remain experimental, and are only to be used for a limited amount of time during an ongoing emergency.
“Pseudouridine likely affects multiple facets of mRNA function, including reduced immune stimulation by several mechanisms, prolonged half-life of pseudouridine-containing RNA, as well as potentially deleterious effects of Ψ on translation fidelity and efficiency.”
Based on the currently available information, it appears to me that the extensive random incorporation of pseudouridine into the synthetic mRNA-like molecules used for the Pfizer/BioNTech and Moderna SARS-CoV-2 vaccines may well account for much or all of the observed immunosuppression, DNA virus reactivation, and remarkable persistence of the synthetic “mRNA” molecules observed in lymph node biopsy tissues (Roltgen et al. 2022). Many of these adverse effects were reported by Kariko, Weissman et al in their 2008 paper “Incorporation of pseudouridine into mRNA yields superior nonimmunogenic vector with increased translational capacity and biological stability” (Kariko et al. 2008) and could have been anticipated by regulatory and toxicology professionals if they had bothered to consider these findings prior to allowing emergency use authorization and widespread (global) deployment of what is truly an immature and previously untested technology. Therefore, neither the FDA, NIH, CDC, nor BioNTech (which employs Dr. Kariko as a Vice President) nor Moderna can claim true ignorance. To my eyes, what we have seen is more appropriately classified as “willful ignorance”.
Based on my review of the scientific data, it is my opinion that the random and uncontrolled insertion of pseudouridine into the manufactured “mRNA”-like molecules creates a population of polymers which may resemble natural mRNA, but which have a variety of properties which are clinically relevant. These characteristics and activities may account for many of the unusual effects, unusual stability, and striking adverse events associated with this new class of vaccines. These molecules are not natural mRNA, and they do not behave like natural mRNA.
The question that most troubles and perplexes me at this point is why the biological consequences of these modifications and associated clinical adverse effects were not thoroughly investigated before widespread administration of random pseudouridine-incorporating “mRNA”-like molecules to a global population.
Biology, and particularly molecular biology, is highly complex and interrelated. Change one thing over here, and it is really hard to predict what might happen over there. That is why one must do rigorously controlled non-clinical and clinical research. Once again, it appears to me that the hubris of “elite” high status scientists, physicians and governmental “public health” bureaucrats has overcome common sense, well established regulatory norms have been disregarded, and patients have unnecessarily suffered as a consequence. These products do not use natural mRNA, and referring to them as mRNA vaccines is misleading. I recommend that, in the future, these products which employ a synthetic unnatural polymer which is not natural mRNA, should be designated using a different term, such as Ψ-mRNA genetic medicines.
CDC Members Own More Than 50 Patents Connected to Vaccinations
The CDC Immunization Safety Office is responsible for investigating the safety and effectiveness of all new vaccinations; once an investigation is considered complete, a recommendation is then made to the CDC’s Advisory Committee on Immunization Practices (ACIP) who then determines whether the new vaccine will be added to the current vaccination schedule. Members of the ACIP committee include physicians such as Dr. Paul Offit, who also serves as the chief of infectious diseases at the Children’s Hospital of Philadelphia. Offit and other CDC members own numerous patents associated with vaccinations and regularly receive funding for their research work from the very same pharmaceutical companies who manufacturer vaccinations which are ultimately sold to the public. This situation creates an obvious conflict of interest, as members of the ACIP committee benefit financially every time a new vaccination is released to the market.
— Read on www.lawfirms.com/resources/environment/environment-health/cdc-members-own-more-50-patents-connected-vaccinations
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.
I’ve come to understand at least 3 major reasons people might have concerns about vaccines:
Volume of vaccines
Volume of vaccine dosages
Vaccine approval rigor
Vaccine trade-off value
Vaccine producers’ lack of financial/legal liability for vaccine injuries
Vaccine as population control
Tax dollars fund Vaccine Injury Programs
Big Pharma Profiteering
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
Measles, mumps, rubella (MMR)
Haemophilus influenzae type b
Today, the vaccine schedule has tripled to fifteen vaccines:
Diphtheria, tetanus, & acellular pertussis
Haemophilus influenzae type b
Influenza (IIV) / Influenza (LAIV)
Measles, mumps, rubella (MMR)
Tetanus, diphtheria, & acellular pertussis
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.
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.
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.
Please note that a similar production already occurred in 1918 as a test run called the Spanish Influenza Epidemic. At the time, it was estimated that twenty (20) million people died of the Spanish Flu, most of them in Europe, and most of them already suffering from starvation.
Now, though nobody appears to know why, the number of deaths from the Spanish Flu, which wasn’t influenza-caused according to the Great Fauci’s own research, has been inflated to (80) million deaths. Other doctors have paired the symptoms recorded during the Spanish Flu with the then-new availability of Bayer Aspirin which was made very widely available and routinely overdosed, which then caused bleeding from the internal organs and mucous membranes, mirroring the symptoms of hemorrhagic fever. Just like other researchers have paired the symptoms and appearance of polio with the appearance of oil-based agricultural pesticides. Miraculously, when these same water-resistant pesticides which are known to cause nerve damage and paralysis were removed from the market, polio also disappeared — purportedly as a result of the polio vaccine. Or not. Just a year prior to the Spanish Flu, Woodrow Wilson, one of the prime architects of all this preposterous fraud, called together the major newspaper owners in this country and formed what he called The Committee on Public Information, (CPI), to spew war propaganda 24/7.
This new government agency also conveniently spewed disinformation about German Americans and Spanish Flu; then as now, there was evidence that the Spanish Flu was given to American Servicemen as innoculations that took place in Kansas, and then spread overseas during the mop-up phase of World War I to decimate both the starving French and German populations— in an apparent attempt to further weaken both nations. This resembles the story we heard at the beginning of all this current madness — that American Servicemen participating in the World Military Games in Wuhan, China, were injected with “vaccines” provided by Fort Detrick, and used as vectors to spread the “Wuhan Disease”—- only it wasn’t the Wuhan Disease. It was, technically, the Fort Detrick Disease.
Additional facts related to Anthony Fauci’s involvement and the use of the pre- prepped and already patented parent viruses (to guarantee that everyone got their share of the profits from this scheme) will be forthcoming in the days to come, and will rip the covers off the coffins. This is not as outrageous as it might seem, when you consider that decades before all this, the British Territorial U.S. Army had distributed blankets purposefully infected with Smallpox to American Indians trapped on Reservations, and Lord Pirbright had similarly used Dutch Prisoners of War as the victims of heinous vaccination experiments at the world’s first-ever concentration camps employed during the Boer War in Africa decades prior to the Spanish Flu.
And reports are pouring in that Big Oil and Big Defense Contractors are already having their “Human Resource” departments comb through the personnel records to identify those who received these experimental shots — and plan to replace them “within three to five years”. Remember Lord Pirbright, mentioned above, a Rothschild toady who committed genocide and created the first-ever concentration camps and forced “medical” experiments during the Boer War? Well, fellas, guess what? The Pirbright Institute named after this Ghoul also had a hand in the current mess. Yes, they funded research that resulted in patents directly related to this “outbreak” for their own financial benefit and for the benefit of their sister organization, the Wellcome Trust. And, then, they passed off the hot potato (the one with a crown) to their American Cousins, who further developed and patented coronavirus strains at Duke University and the University of North Carolina at Chapel Hill (thanks to more “philanthropic” funding) which all ended up at Fort Detrick and the NIH and resulted in still more patents benefiting the Vermin ….and, finally, together with over 3 million taxpayer dollars in research funding provided by Dr. Anthony Fauci— found its way to Wuhan, China, too. Now, did this virulent “enhanced” germ escape from the lab in Wuhan, or was it delivered to Wuhan by our own servicemen who had been unknowingly injected with it? Probably both means were used, and all to the same ends: trying to make it look like the Chinese were to blame for the pandemic and all the economic upheaval and losses created by this opportunistic furor.
Once again, if you dig deep enough, you find Brits…. monotonously, always, front- and-center, at the bottom of every dogpile. One should also brace for the Chinese to nationalize all those investments made by western companies in China since 1971 and for China to continue to withdraw for a time into its borders, even as it strives to build new trade relationships with new partners in South America and Australia and Africa and India and Russia. Remember what I told you about how our own Western Parasites have been in the process of killing their host (America) and moving on to greener pastures in China for the past fifty years, including an obvious intention to use the “million man surplus” army they created in China with their “one child” policy, to replace their cheap American mercenaries with even cheaper Chinese throw-aways? The Chinese read the tea leaves. It means that they are stuck with the investment costs of 70 million new housing units, and the only way they can make up the deficit is by nationalizing western investment enterprises —or spending the gold they have been at such pains to accumulate. Go figure what you would do, in their shoes? Let’s see, these heinous abuses of people started with the Brits (British Territorial U.S. Smallpox blankets and Lord Pirbright and Boer War experiments and concentration camps) and continued with the Brits (Pirbright Institute and Wellcome Trust) and then continued with British Sympathizers (Harvard’s Charles Lieber and the Fat Man from Chapel Hill) and then onward to British Territorial operatives at Fort Detrick. All in succession, all neatly documented through the Patent Offices and incorporation records for the better part of a hundred years — and most of it all connected by and through one organization operating in both Great Britain and America: The Pilgrims Society, and a long list of prominent Eugenicists.
So, you see, we have been to this rodeo before, and it is a uniquely British style rodeo, where the victims are blamed, and the today elitist scumbags are rewarded, and the weak — especially the young and the old of the “herd” are preyed upon by cowards wearing white coats and wielding needles.
66% of self-defined “swing” voters in competitive districts believe that “Democrats in Congress have taken things too far in their pandemic response.”.
👆This is exactly why Democrats are suddenly lifting restrictions👆
White and Hispanic voters were in equal agreement.
80% of these same swing voters believe that “Democrats in Congress support defunding the police and taking more cops off of the street.”
78% of these swing voters believe that “Democrats in Congress have created a border crisis that allows illegal immigrants to enter the country without repercussions and grants them tax-payer funded benefits once here.”
61% of these swing district voters believe that “Democrats in Congress are spending money out of control,”
“Democrats are teaching kids as young as five Critical Race Theory, which teaches that America is a racist country and that white people are racist.”
👉The poll was conducted from mid-January to early February, had approximately 1,000 respondents and a 3.1% margin of error.
The Democratic Congressional Campaign Committee (DCCC) is concerned that Republican attacks on the Democrats’ handling of the COVID-19 pandemic have “alarming credibility,” according to a slide deck obtained by SFGATE.
The DCCC, which is the main campaign arm for House Democrats and is currently chaired by New York Rep. Sean Patrick Maloney, worked with outside consulting groups to conduct an online poll of voters in the 60 most competitive House districts for the upcoming 2022 midterms. The poll was conducted from mid-January to early February, had approximately 1,000 respondents and a 3.1% margin of error.
Findings from the poll were presented to DCCC officials Thursday morning. One slide in the presentation, which was shared with SFGATE by someone who attended the presentation and was granted anonymity in accordance with Hearst’s ethics policy, states, “Many of the Republican attacks tested have alarming credibility,” including Republican attacks on COVID-19 policy. (The presentation does not clarify what it means by “credibility.”)
The poll found that that 57% of voters in competitive congressional districts agree with the statement, “Democrats in Congress have taken things too far in their pandemic response,” and 66% of self-defined “swing” voters in competitive districts agree with that statement. White and Hispanic voters in competitive districts were equally as likely to agree (59%), while Black voters (42%) and Asian voters (46%) disagreed with the statement. The poll also did not define what “taken things too far” means.
The DCCC found that critiques of COVID-19 restrictions were slightly less potent than other issues. In swing districts, 64% of voters agreed with the statement that “Democrats in Congress support defunding the police and taking more cops off of the street.” The internal poll found that 80% of self-defined swing voters in competitive districts agreed with the same statement. Politico previously reported on the DCCC warning about the effectiveness of what they refer to as conservative “culture war attacks.”
Sixty-two percent of voters in contested districts agreed with the statement, “Democrats in Congress have created a border crisis that allows illegal immigrants to enter the country without repercussions and grants them tax-payer funded benefits once here.” Seventy-eight percent of swing voters in those districts agreed.
Sixty-one percent of swing district voters agreed with the statements, “Democrats in Congress are spending money out of control,” and, “Democrats are teaching kids as young as five Critical Race Theory, which teaches that America is a racist country and that white people are racist.” And 59% agreed with the statement, “Democrats are too focused on pursuing an agenda that divides us and judging those who don’t see things their way.”
The slide deck provides a snapshot into some of Democrats’ strategies as their outlook for the 2022 midterms growsincreasinglygrim.
The DCCC presentation also contained a slide showing that the top two concerns of voters in competitive districts are inflation and health care, with the COVID-19 pandemic coming in third. Medicare/social security and climate change rounded out the top five. At the bottom of the list were voting rights, taxes and racial justice/equality.