Bill Gates: Covid-19 Vaccines Don't Stop Transmission, 'New Way of Doing Vaccines, Pivot to 'Cures'
Updated: Nov 24, 2021
The blog is temporarily breaking hiatus for an important 'Head's Up' article:
The Covid-19 Vaccination propaganda campaign is pivoting from a Covid-19 vaccination focus into the WHO's 'four prong' management approach.. And, much of the vaccine opposition leadership is selling the pitch.
The Gates Foundation has been financing the 'cures' now being promoted by 'independent media' (scroll down to bottom of second half of report)
It is clear we are about to enter a new phase of the Covid-19 global reset campaign when the lead salesman for the global controllers openly admits Covid-19 vaccines do not stop transmission of disease:
The full interview may be viewed HERE:
In this interviewer, Gates also expressed support for the totalitarian & draconian Covid-19 measures currently being imposed in New Zealand and Australia:
“At least Australia and New Zealand showed that competent management could keep the death rate down pretty dramatically,” he said in the interview.
(scroll down to bottom of this post for recent developments around Gates new small pox vaccine campaign & R/D funding campaign which coincide with FBI investigations of a small pox related virus in a Merck lab - under update)
Australia has now placed 1/3rd of its (unvaccinated) population under lockdown and built double electrified fence 'quarantine facilities': (footage from Queensland Australia)
This is despite nurse whistleblowers openly stating to the news media hospitals are full of the vaccine injured, not Covid-19 cases:
This would be comical if it wasn't so serious as the 'vaccines' never were designed to prevent transmission of disease, only induce suppress symptoms of attributed Covid-19 illness. Dr Anthony Fauci openly admitted from day 1:
"Dr. Anthony Fauci explained in an interview that the actual goal of the early COVID-19 vaccines isn’t even to block infections, a detail that people should be aware of even before considering whether to get a vaccine or which vaccine to go for. Instead, scientists are aiming to prevent severe COVID-19 cases or stop symptoms altogether. The virus would still gain entry into the human body, but vaccines will stop it from replicating and prevent symptoms, including life-threatening complications". (the last statement is a documented fallacy as testing monitored mild cases and did not monitor for reduction in severe outcomes/hospitalizations/deaths as outlined from the BMJ HERE)
Objective review of vaccine trial/public health organization data document Covid-19 inoculations induce greater rates/severity of side effects mirroring the symptoms they are purported to suppress as documented HERE.
Worse, Covid-19 has been manufactured as a disease of attribution to other cause through testing peer reviewed by 22 panel experts for the International Consortium of Science as 'useless for the purpose.
A vaccine can not suppress symptoms or stop transmission of a disease which has been created through fabricated testing and rigged attribution standards nor any pharmaceutical drug cure it.
The CDC/WHO protocols are DESIGNED to capture/create/assign Covid-19 to Sars CoV2 through unscientific standards which, in a world truly governed by objective 'science' would be immediately denounced as FRAUD.
Hospitals have been INCENTIVIZED to falsely label hospitalizations and mortalities as Covid. The Association of Physicians and Surgeons issued a report on organization's website on 11/17/2021 documenting the payment incentives:
The hospital payments include:
A “free” required PCR test in the Emergency Room or upon admission for every patient, with government-paid fee to hospital. (PCR testing is unsuitable for detection of Sars CoV2)
Added bonus payment for each positive COVID-19 diagnosis.
Another bonus for a COVID-19 admission to the hospital.
A 20 percent “boost” bonus payment from Medicare on the entire hospital bill for use of remdesivir instead of medicines such as Ivermectin.
Another and larger bonus payment to the hospital if a COVID-19 patient is mechanically ventilated.
More money to the hospital if cause of death is listed as COVID-19, even if patient did not die directly of COVID-19.
A COVID-19 diagnosis also provides extra payments to coroners.
Remdesivir is both ineffective and deadly.
Despite the WHO advising AGAINST Remdesivir for patients hospitalized with Covid-19 attributed infections LAST November, the drug continues to be implemented as part of hospital standard treatment protocol.
Treatment protocols and DNR have been implicated in the large numbers of early death in care homes and hospitals as documented HERE.
Unfortunately, many of the self appointed leadership of the vaccine mandate and opposition movement, have utterly failed to point out the most basic and central flaws with the MSM Covid-19 narrative. Indeed, many of their new talking points align perfectly with the World Health Organization 'four prong' approach strategy.
"He urged countries to have robust surveillance to find, isolate, test and treat every case, to break the chains of transmission"
The testing program is creating the cases.
(no drug can cure a false positive test or misattribution of another illness to Covid-19)
This multi-prong approach format is designed to perpetuate a testing program which needs to IMMEDIATELY cease, continue to manufacturer 'cases' to provide the political rationale for medical passports/mass government surveillance/quarantine, and economic rationale for government financing of more harmful and unnecessary drug interventions.
This WHO outline strategy is the. underpinning for the new Covid-19 buzzwords appearing in the media (msm/independent media alike)
To be clear, this blog wholeheartedly agrees with the concept of innate healing through natural immune system response.
HOWEVER, natural immunity is now being used as a propaganda sales pitch to rationalize more Covid-19 testing which is MANUFACTURING the cases. The Defender recently highlighted research showing the superiority of natural immunity over vaccines to protect from Covid-19.
81 Research Studies Confirm Natural Immunity to COVID ‘Equal’ or ‘Superior’ to Vaccine Immunity
None of these research studies (or ANY study) utilizing testing non specific to the virus, developed without virus isolate, and set at amplification cycles over 24 CT (the rate research has shown to pick up NO live material) have ANY scientific validity. None.
The PCR test for ascertaining infection with Sars CoV2 is useless for the purpose and thus ALL studies utilizing PCR are fatally corrupted and render all these studies null and void.
The 'natural immunity' narrative is laying the foundation for the requirement to continually document our health status to the government through a continued testing program. It will also continue to churn out fabricated cases which will providing the political and economic rationale for entirely new 'treatment' interventions.
It is concerning that so many of those opposed to Covid-19 vaccination passports are accepting 'testing' as a suitable alternative as both are:
a. mechanisms to prove health status to the government
b. interventions designed to limit/monitor movement based on health status.
Companion blog: (nearly all Covid-19 testing released since the inception of the program has been subsequently recalled by the FDA- the testing program is an open scandal and "opposition" leadership reinforcement of management of the 'crisis' through testing is perpetuating the scam):
Contaminated Covid-19 Tests, Hundreds of Millions Recalled, Implicated India Black Fungal Outbreak, FDA RECALLS
Early Treatment & Cures
As the testing and un-scientific attribution standards are driving the 'cases' and not infection, there is ZERO need for any new (or old) pharmaceutical cure or treatment.
It is highly troubling that the lead vaccine opposition narrative is transforming to push more Gates Foundation financed drug 'cures' instead of exposing the central fraud of the existing narrative.
The new buzzword of 'early treatment' is deeply problematic.
Even if one ascribes completely to the official Covid narrative, early treatment of Covid-19 makes zero logical sense.
86% of Covid-19 'cases' were found in an Oxford study to have NO core symptoms of Covid-19 whatsoever (this is due to the faulty testing, not 'silent infection' as claimed in this article, however sharing to document majority of Covid-19 attributed infections have NO symptoms anyway)
"The study, which was peer reviewed, looked at 36,061 individuals who took a coronavirus test as part of the infection survey between 26 April and 27 June 2020. It found that 86.1% of those who tested positive for the virus did not report “core” symptoms associated with the virus (a cough, fever or a loss of taste and/or smell) on the day they took a test. Out of the 115 people that received a positive coronavirus result, only 16 reported the main symptoms that we associate with the virus". (see companion blog, no Asymptomatic Transmission)
The push for vaccines for Covid-19 attributed infections has always been farcical. The majority have no symptoms anyway, those who do are overwhelmingly mild, and the vaccine trials studied for mild not severe outcomes, so there is ZERO substantive evidence of these unnecessary & harmful drugs provide ANY substantive benefit despite the endless propaganda narrative 'Vaccine Saves Lives'.
So, even if one completely ascribes to the 'official' Covid-19 MSM narrative (which this blog in no way does), there is NO logical rationale for mass pharmaceutical intervention for Covid-19 attributed cases which hardly every are attributed to a severe outcome with the majority expressing NO symptoms.
It is utter absurdity.
And, for those in the vaccine opposition community who are fully aware of the severe Covid-19 testing flaws and attribution standards, it is troubling that so many are now ascribing to testing and DIFFERENT pharmaceutical drugs as the necessary solution for management of Covid-19 (again, drugs/vaccines can not treat/cure/prevent a false positive test)!
Gates Foundation Funded Covid-19 'Cures' Replacing Gates Foundation Funded 'Vaccines'
Monoclonal Antibody Therapy:
Long Term Research Initiative and Funding by the Bill and Melinda Gates Foundation for MAT goes back to 2011:
Developing Monoclonal Antibodies for Global Health
Visterra was acquired by Otsuka Pharmaceutical in September 2018, six years after the foundation’s initial investment. In between there were highs, including the U.S. Government Biomedical Advanced Research and Development Authority awarding Visterra with an up to $204.5 million grant for clinical trials of its promising flu monoclonal antibody therapy as well as strategic partnerships with A*STAR in Singapore, Serum Institute of India and Vir Biotechnology in San Francisco. There were also lows, including two failed initial public offerings and ongoing struggles accessing venture capital as an infectious disease-focused company. Through it all, Visterra’s management team, board and investors were steadfast foundation partners focusing on good science and working with world experts to systematically interrogate the potential of the Visterra platform for global health. As part of the $430 million Otsuka Pharmaceutical acquisition, the foundation has the right to bring highly promising mAb vaccine candidates to the Visterra team to attempt to increase their half-life. Additionally, the antibody drug conjugate development program will continue.
Despite the Gates Foundation claims of monoclonal antibody safety, these drugs are NOT safe and document severe health side effects which parallel Covid-19 vaccination risks including:
Acute infusion reactions can be caused by a range of mechanisms including anaphylaxis, anaphylactoid reactions, serum sickness, tumour lysis syndrome and cytokine release syndrome.
mAbs against tumour necrosis factor-α (TNFα) have been associated with reactivation of latent tuberculosis, as well as with other serious infections and malignancies.
Progressive multifocal leukoencephalopathy is a rare but serious complication of natalizumab (Tysabri; Biogen Idec, Elan), rituximab (Rituxan/MabThera; Genentech, Biogen Idec) and efalizumab (Raptiva; Genentech).
Treatment with abciximab (ReoPro; Centocor Ortho Biotech, Eli Lilly), an antiplatelet glycoprotein IIb/IIIa chimeric Fab antibody fragment, can cause thrombocytopaenia; although it can also be caused by various other mAbs due to immune thrombocytopaenia.
mAbs directed against TNFα can cause a lupus-like syndrome; alemtuzumab (Campath; Genzyme) can mediate thyroid disease through autoimmunity; and mAbs directed against cytotoxic T-lymphocyte-associated antigen 4 (CTLA4) can initiate autoimmune colitis.
mAbs against human epidermal growth factor receptor commonly cause skin rashes, while trastuzumab (Herceptin; Genentech), an ERBB2-specific mAb, can cause cardiotoxicity.
The dramatic cytokine storm seen after infusion of TGN1412 (a CD28 superagonist) has resulted in the recommendation of a range of measures to improve the safety of first-in-human clinical testing with mAbs.
This technology has now been Emergency Use Approved for treating MILD to MODERATE Covid-19 attributed infection.
This is an EUA drug which is targeting vulnerable children and pregnant women:
The following medical conditions or other factors may place adults and pediatric patients (age 12-17 years and weighing at least 40 kg) at higher risk for progression to severe COVID-19:
• Older age (for example, age ≥65 years of age)
• Obesity or being overweight (for example, BMI >25 kg/m2 , or if age 12-17, have BMI ≥85th percentile for their age and gender based on CDC growth charts, https://www.cdc.gov/growthcharts/clinical_charts.htm)
• Pregnancy • Chronic kidney disease
• Diabetes • Immunosuppressive disease or immunosuppressive treatment
• Cardiovascular disease (including congenital heart disease) or hypertension • Chronic lung diseases (for example, chronic obstructive pulmonary disease, asthma [moderate-to-severe], interstitial lung disease, cystic fibrosis and pulmonary hypertension)
• Sickle cell disease • Neurodevelopmental disorders (for example, cerebral palsy) or other conditions that confer medical complexity (for example, genetic or metabolic syndromes and severe congenital anomalies) • Having a medical-related technological dependence (for example, tracheostomy, gastrostomy, or positive pressure ventilation (not related to COVID-19))
The drug has been touted for 'early treatment' but has been shown to be associated with WORSE outcomes.
They are INFUSING this into pregnant women, children, and individuals who are immunocompromised and vulnerable.
Signs and symptoms of infusion-related reactions may include: fever, difficulty breathing, reduced oxygen saturation, chills, nausea, arrhythmia (e.g., atrial fibrillation, tachycardia, bradycardia), chest pain or discomfort, weakness, altered mental status, headache, bronchospasm, hypotension, hypertension, angioedema, throat irritation, rash including urticaria, pruritus, myalgia, vasovagal reactions (e.g., pre-syncope, syncope), dizziness, fatigue and diaphoresis. Consider slowing or stopping the infusion and administer appropriate medications and/or supportive care if an infusion-related reaction occurs
Clinical Worsening After REGEN-COV Administration: Clinical worsening of COVID-19 after administration of REGEN-COV has been reported and may include signs or symptoms of fever, hypoxia or increased respiratory difficulty, arrhythmia (e.g., atrial fibrillation, tachycardia, bradycardia), fatigue, and altered mental status. Some of these events required hospitalization. It is not known if these events were related to REGEN-COV use or were due to progression of COVID-19
Limitations of Benefit and Potential for Risk in Patients with Severe COVID-19: Monoclonal antibodies, such as REGEN-COV, may be associated with worse clinical outcomes when administered to hospitalized patients with COVID-19 requiring high-flow oxygen or mechanical ventilation. Therefore, REGEN-COV is not authorized for use in patients who are hospitalized due to COVID-19, OR who require oxygen therapy due to COVID-19, OR who require an increase in baseline oxygen flow rate due to COVID-19 in those on chronic oxygen therapy due to underlying non-COVID-19–related comorbidity
Monoclonal Antibodies are unethical/illegal violation of Nuremberg code. The EUA allows administration to populations not at attributed severe risk of Covid-19 infection attributed outcomes, there is no 'emergency' to justify this authorization, and all participants are being enrolled as part of a 'defacto' medical trial as the evidence and data collected will inform final medical approval.
Gates Financing Ivermectin Studies for the Treatment of Covid-19
GATES FUNDS RIVER BLINDNESS PROGRAM (ivermectin)
Ivermectin has been touted as a safe and effective drug to manage Covid-19 symptoms. Its proponents tout reduced severe outcomes on the basis of scientifically invalidated studies utilizing PCR tests for detection of Sars CoV2 (diagnosis) and end point outcome measurement. The studies promoting Ivermectin equally flawed as vaccine trial data.
Proponents claiming success with Ivermectin, fail to disclose that the drugs offer no purported benefit over what an individual will already experience with a positive PCR test diagnosis for Covid-19 attributed infection.
Ivermectin has been documented to induce neurotoxicity and ocular damage in studies monitoring the administration of the drug in mass administration in Africa for treatment of 'River Blindness' (pre-Covid). Ivermectin is a fourth generation drug for the treatment of 'River Blindness' formerly known as Craw Craw and blindness was never associated with the disease until the introduction of pharmacological drugs and mass DTT spraying began in the 1940s.
Other drugs administered in this (River Blindness) program have been documented to induce severe fertility issues, please see full report of this issue with source links HERE.
Gates Foundation & the Covid-19 Pill:
"The Bill & Melinda Gates Foundation will provide up to $120 million to help lower-income countries access a new pill to treat COVID-19, the foundation announced Tuesday:.
Gates Foundation Announcing the COVID-19 Therapeutics Accelerator
"That is why today, we are joining forces with Wellcome and Mastercard to beef up our response—backed by $125 million in both new funding and money already earmarked to tackle this epidemic. The money will be used to identify potential treatments for COVID-19, accelerate their development, and prepare for the manufacture of millions of doses for use worldwide. The expertise of pharmaceutical companies will be critical to this endeavor, named the COVID-19 Therapeutics Accelerator".
Bill Gates & George Soros partner to purchase testing company:
George Soros and Bill Gates Just Teamed Up to Buy a COVID Company
How Bill Gates Funded the Science Fraud in the Imperial College Covid Model
Google any new drug treatment/vaccine or treatment method for Covid-19 and the Bill and Melinda Gates foundation is going to come up up as lead financiers. It is imperative those opposing harmful vaccination and mandate policies do not accept another version of the same control mechanisms under the guise of 'testing' & 'treatment'.
The vaccine opposition community is heading in a dangerous direction by following leads pushing the lingo and pharmaceuticals of the WHO and the Bill and Melinda Gates foundation. The solution to a crisis manufactured through faulty testing and unscientific standards is exposure of the foundational fraud, not drugs or tests.
The cure for Covid-19 is simple. End the testing and expose the fraud.
Please pass this article along and be careful not to be baited to speak in the newspeak language of the latest lie.