(WATCH) ‘63% of Covid Delta deaths in UK since Feb. were among fully vaccinated’

Sen. Ron Johnson (R-Wisconsin) says that public health data from England shows:

In the UK over the past 7.5 months:

There were 750,000 new Covid cases

80% of them (about 600,000) were Delta variant

There 2,542 deaths among the cases

Most of the victims, 1,613, were fully vaccinated

28% were unvaccinated

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32 thoughts on “(WATCH) ‘63% of Covid Delta deaths in UK since Feb. were among fully vaccinated’”

  1. Your Article here about re-infections, You can Share what I think is going on here. “What I believe in the 63% re infections in UK is the Results of ( Virus Homologous Recombination = Time / Antibodies ) > is the Culprit going on in People who was already Vaccinated. Example Riboviria -use a Homologous RNA- dependent polymerase for Replication so you end up with A Delta Virus Homologous Recombination >> ” That Wascally determined Strain over other Stain of Variants “.

    1. I will go with French Virologist and Nobel Prize Winner Luc Montagnier who contends that “it is the vaccination that is creating the variants.” Seems pretty logical then that it is the vaccinated getting sick with a new variant.

      The anonymous author of this goes by the name Spartacus. He is anonymous for a reason. It’s because the left destroys people like Spartacus. This time, sadly, the left are ruining people with the help of our brethren. Some of our fellow conservatives have fallen under the spell of the same evil people that peddle global warming and have been helping sell their propaganda. How did this happen?

      This is sobering for the jabbed, I understand. But one thing should be clear, the protocols our doctors are following in this country are wrong. They are killing people.

      COVID-19 is a blood and blood vessel disease. SARS-CoV-2 infects the lining of human blood vessels, causing them to leak into the lungs.
      Current treatment protocols (e.g. invasive ventilation) are actively harmful to patients, accelerating oxidative stress and causing severe VILI (ventilator-induced lung injuries). The continued use of ventilators in the absence of any proven medical benefit constitutes mass murder.
      Existing countermeasures are inadequate to slow the spread of what is an aerosolized and potentially wastewater-borne virus, and constitute a form of medical theater.
      Various non-vaccine interventions have been suppressed by both the media and the medical establishment in favor of vaccines and expensive patented drugs.
      The authorities have denied the usefulness of natural immunity against COVID-19, despite the fact that natural immunity confers protection against all of the virus’s proteins, and not just one.
      Vaccines will do more harm than good. The antigen that these vaccines are based on, SARS-CoV- 2 Spike, is a toxic protein. SARS-CoV-2 may have ADE, or antibody-dependent enhancement; current antibodies may not neutralize future strains, but instead help them infect immune cells. Also, vaccinating during a pandemic with a leaky vaccine removes the evolutionary pressure for a virus to become less lethal.
      There is a vast and appalling criminal conspiracy that directly links both Anthony Fauci and Moderna to the Wuhan Institute of Virology.
      COVID-19 vaccine researchers are directly linked to scientists involved in brain-computer interface (“neural lace”) tech, one of whom was indicted for taking grant money from China.
      Independent researchers have discovered mysterious nanoparticles inside the vaccines that are not supposed to be present.
      The entire pandemic is being used as an excuse for a vast political and economic transformation of Western society that will enrich the already rich and turn the rest of us into serfs and untouchables.
      COVID-19 Pathophysiology and Treatments:
      COVID-19 is not a viral pneumonia. It is a viral vascular endotheliitis and attacks the lining of blood vessels, particularly the small pulmonary alveolar capillaries, leading to endothelial cell activation and sloughing, coagulopathy, sepsis, pulmonary edema, and ARDS-like symptoms. This is a disease of the blood and blood vessels. The circulatory system. Any pneumonia that it causes is secondary to that.

      In severe cases, this leads to sepsis, blood clots, and multiple organ failure, including hypoxic and inflammatory damage to various vital organs, such as the brain, heart, liver, pancreas, kidneys, and intestines.

      Some of the most common laboratory findings in COVID-19 are elevated D-dimer, elevated prothrombin time, elevated C-reactive protein, neutrophilia, lymphopenia, hypocalcemia, and hyperferritinemia, essentially matching a profile of coagulopathy and immune system hyperactivation/immune cell exhaustion.

      COVID-19 can present as almost anything, due to the wide tropism of SARS-CoV-2 for various tissues in the body’s vital organs. While its most common initial presentation is respiratory illness and flu-like symptoms, it can present as brain inflammation, gastrointestinal disease, or even heart attack or pulmonary embolism.

      COVID-19 is more severe in those with specific comorbidities, such as obesity, diabetes, and hypertension. This is because these conditions involve endothelial dysfunction, which renders the circulatory system more susceptible to infection and injury by this particular virus.

      The vast majority of COVID-19 cases are mild and do not cause significant disease. In known cases, there is something known as the 80/20 rule, where 80% of cases are mild and 20% are severe or critical. However, this ratio is only correct for known cases, not all infections. The number of actual infections is much, much higher. Consequently, the mortality and morbidity rate is lower. However, COVID-19 spreads very quickly, meaning that there are a significant number of severely-ill and critically-ill patients appearing in a short time frame.

      In those who have critical COVID-19-induced sepsis, hypoxia, coagulopathy, and ARDS, the most common treatments are intubation, injected corticosteroids, and blood thinners. This is not the correct treatment for COVID-19. In severe hypoxia, cellular metabolic shifts cause ATP to break down into hypoxanthine, which, upon the reintroduction of oxygen, causes xanthine oxidase to produce tons of highly damaging radicals that attack tissue. This is called ischemia-reperfusion injury, and it’s why the majority of people who go on a ventilator are dying. In the mitochondria, succinate buildup due to sepsis does the same exact thing; when oxygen is reintroduced, it makes superoxide radicals. Make no mistake, intubation will kill people who have COVID-19.

      The end-stage of COVID-19 is severe lipid peroxidation, where fats in the body start to “rust” due to damage by oxidative stress. This drives autoimmunity. Oxidized lipids appear as foreign objects to the immune system, which recognizes and forms antibodies against OSEs, or oxidation-specific epitopes. Also, oxidized lipids feed directly into pattern recognition receptors, triggering even more inflammation and summoning even more cells of the innate immune system that release even more destructive enzymes. This is similar to the pathophysiology of Lupus.

      COVID-19’s pathology is dominated by extreme oxidative stress and neutrophil respiratory burst, to the point where hemoglobin becomes incapable of carrying oxygen due to heme iron being stripped out of heme by hypochlorous acid. No amount of supplemental oxygen can oxygenate blood that chemically refuses to bind O2.

      The breakdown of the pathology is as follows:

      SARS-CoV-2 Spike binds to ACE2. Angiotensin Converting Enzyme 2 is an enzyme that is part of the renin-angiotensin-aldosterone system, or RAAS. The RAAS is a hormone control system that moderates fluid volume in the body and in the bloodstream (i.e. osmolarity) by controlling salt retention and excretion. This protein, ACE2, is ubiquitous in every part of the body that interfaces with the circulatory system, particularly in vascular endothelial cells and pericytes, brain astrocytes, renal tubules and podocytes, pancreatic islet cells, bile duct and intestinal epithelial cells, and the seminiferous ducts of the testis, all of which SARS-CoV-2 can infect, not just the lungs.

      SARS-CoV-2 infects a cell as follows: SARS-CoV-2 Spike undergoes a conformational change where the S1 trimers flip up and extend, locking onto ACE2 bound to the surface of a cell. TMPRSS2, or transmembrane protease serine 2, comes along and cuts off the heads of the Spike, exposing the S2 stalk-shaped subunit inside. The remainder of the Spike undergoes a conformational change that causes it to unfold like an extension ladder, embedding itself in the cell membrane. Then, it folds back upon itself, pulling the viral membrane and the cell membrane together. The two membranes fuse, with the virus’s proteins migrating out onto the surface of the cell. The SARS-CoV-2 nucleocapsid enters the cell, disgorging its genetic material and beginning the viral replication process, hijacking the cell’s own structures to produce more virus.

      SARS-CoV-2 Spike proteins embedded in a cell can actually cause human cells to fuse together, forming syncytia/MGCs (multinuclear giant cells). They also have other pathogenic, harmful effects. SARS-CoV- 2’s viroporins, such as its Envelope protein, act as calcium ion channels, introducing calcium into infected cells. The virus suppresses the natural interferon response, resulting in delayed inflammation. SARS-CoV-2 N protein can also directly activate the NLRP3 inflammasome. Also, it suppresses the Nrf2 antioxidant pathway. The suppression of ACE2 by binding with Spike causes a buildup of bradykinin that would otherwise be broken down by ACE2.

      This constant calcium influx into the cells results in (or is accompanied by) noticeable hypocalcemia, or low blood calcium, especially in people with Vitamin D deficiencies and pre-existing endothelial dysfunction. Bradykinin upregulates cAMP, cGMP, COX, and Phospholipase C activity. This results in prostaglandin release and vastly increased intracellular calcium signaling, which promotes highly aggressive ROS release and ATP depletion. NADPH oxidase releases superoxide into the extracellular space. Superoxide radicals react with nitric oxide to form peroxynitrite. Peroxynitrite reacts with the tetrahydrobiopterin cofactor needed by endothelial nitric oxide synthase, destroying it and “uncoupling” the enzymes, causing nitric oxide synthase to synthesize more superoxide instead. This proceeds in a positive feedback loop until nitric oxide bioavailability in the circulatory system is depleted.

      Dissolved nitric oxide gas produced constantly by eNOS serves many important functions, but it is also antiviral against SARS-like coronaviruses, preventing the palmitoylation of the viral Spike protein and making it harder for it to bind to host receptors. The loss of NO allows the virus to begin replicating with impunity in the body. Those with endothelial dysfunction (i.e. hypertension, diabetes, obesity, old age, African-American race) have redox equilibrium issues to begin with, giving the virus an advantage.

      Due to the extreme cytokine release triggered by these processes, the body summons a great deal of neutrophils and monocyte-derived alveolar macrophages to the lungs. Cells of the innate immune system are the first-line defenders against pathogens. They work by engulfing invaders and trying to attack them with enzymes that produce powerful oxidants, like SOD and MPO. Superoxide dismutase takes superoxide and makes hydrogen peroxide, and myeloperoxidase takes hydrogen peroxide and chlorine ions and makes hypochlorous acid, which is many, many times more reactive than sodium hypochlorite bleach.

      Neutrophils have a nasty trick. They can also eject these enzymes into the extracellular space, where they will continuously spit out peroxide and bleach into the bloodstream. This is called neutrophil extracellular trap formation, or, when it becomes pathogenic and counterproductive, NETosis. In severe and critical COVID-19, there is actually rather severe NETosis.

      Hypochlorous acid building up in the bloodstream begins to bleach the iron out of heme and compete for O2 binding sites. Red blood cells lose the ability to transport oxygen, causing the sufferer to turn blue in the face. Unliganded iron, hydrogen peroxide, and superoxide in the bloodstream undergo the Haber- Weiss and Fenton reactions, producing extremely reactive hydroxyl radicals that violently strip electrons from surrounding fats and DNA, oxidizing them severely.

      This condition is not unknown to medical science. The actual name for all of this is acute sepsis.

      We know this is happening in COVID-19 because people who have died of the disease have noticeable ferroptosis signatures in their tissues, as well as various other oxidative stress markers such as nitrotyrosine, 4-HNE, and malondialdehyde.

      When you intubate someone with this condition, you are setting off a free radical bomb by supplying the cells with O2. It’s a catch-22, because we need oxygen to make Adenosine Triphosphate (that is, to live), but O2 is also the precursor of all these damaging radicals that lead to lipid peroxidation.

      The correct treatment for severe COVID-19 related sepsis is non-invasive ventilation, steroids, and antioxidant infusions. Most of the drugs repurposed for COVID-19 that show any benefit whatsoever in rescuing critically-ill COVID-19 patients are antioxidants. N-acetylcysteine, melatonin, fluvoxamine, budesonide, famotidine, cimetidine, and ranitidine are all antioxidants. Indomethacin prevents iron- driven oxidation of arachidonic acid to isoprostanes. There are powerful antioxidants such as apocynin that have not even been tested on COVID-19 patients yet which could defang neutrophils, prevent lipid peroxidation, restore endothelial health, and restore oxygenation to the tissues.

      Scientists who know anything about pulmonary neutrophilia, ARDS, and redox biology have known or surmised much of this since March 2020. In April 2020, Swiss scientists confirmed that COVID-19 was a vascular endotheliitis. By late 2020, experts had already concluded that COVID-19 causes a form of viral sepsis. They also know that sepsis can be effectively treated with antioxidants. None of this information is particularly new, and yet, for the most part, it has not been acted upon. Doctors continue to use damaging intubation techniques with high PEEP settings despite high lung compliance and poor oxygenation, killing an untold number of critically ill patients with medical malpractice.

      Because of the way they are constructed, Randomized Control Trials will never show any benefit for any antiviral against COVID-19. Not Remdesivir, not Kaletra, not HCQ, and not Ivermectin. The reason for this is simple; for the patients that they have recruited for these studies, such as Oxford’s ludicrous RECOVERY study, the intervention is too late to have any positive effect.

      The clinical course of COVID-19 is such that by the time most people seek medical attention for hypoxia, their viral load has already tapered off to almost nothing. If someone is about 10 days post-exposure and has already been symptomatic for five days, there is hardly any virus left in their bodies, only cellular damage and derangement that has initiated a hyperinflammatory response. It is from this group that the clinical trials for antivirals have recruited, pretty much exclusively.

      In these trials, they give antivirals to severely ill patients who have no virus in their bodies, only a delayed hyperinflammatory response, and then absurdly claim that antivirals have no utility in treating or preventing COVID-19. These clinical trials do not recruit people who are pre-symptomatic. They do not test pre-exposure or post-exposure prophylaxis.

      This is like using a defibrillator to shock only flatline, and then absurdly claiming that defibrillators have no medical utility whatsoever when the patients refuse to rise from the dead. The intervention is too late. These trials for antivirals show systematic, egregious selection bias. They are providing a treatment that is futile to the specific cohort they are enrolling.

      India went against the instructions of the WHO and mandated the prophylactic usage of Ivermectin. They have almost completely eradicated COVID-19. The Indian Bar Association of Mumbai has brought criminal charges against WHO Chief Scientist Dr. Soumya Swaminathan for recommending against the use of Ivermectin.

      Ivermectin is not “horse dewormer”. Yes, it is sold in veterinary paste form as a dewormer for animals. It has also been available in pill form for humans for decades, as an antiparasitic drug.

      The media have disingenuously claimed that because Ivermectin is an antiparasitic drug, it has no utility as an antivirus. This is incorrect. Ivermectin has utility as an antiviral. It blocks importin, preventing nuclear import, effectively inhibiting viral access to cell nuclei. Many drugs currently on the market have multiple modes of action. Ivermectin is one such drug. It is both antiparasitic and antiviral.

      In Bangladesh, Ivermectin costs $1.80 for an entire 5-day course. Remdesivir, which is toxic to the liver, costs $3,120 for a 5-day course of the drug. Billions of dollars of utterly useless Remdesivir were sold to our governments on the taxpayer’s dime, and it ended up being totally useless for treating hyperinflammatory COVID-19. The media has hardly even covered this at all.

      The opposition to the use of generic Ivermectin is not based in science. It is purely financially and politically-motivated. An effective non-vaccine intervention would jeopardize the rushed FDA approval of patented vaccines and medicines for which the pharmaceutical industry stands to rake in billions upon billions of dollars in sales on an ongoing basis.

      The majority of the public are scientifically illiterate and cannot grasp what any of this even means, thanks to a pathetic educational system that has miseducated them. You would be lucky to find 1 in 100 people who have even the faintest clue what any of this actually means.

      1. So ummm if no one will know what it means why waste your time trying to tell people things that they are not equipped to understand?
        I mean aside from you not having any credentials making reading what you posted a waste of their time.

      2. The jab is what is causing the symptoms effecting the cardiovascular system and organs. Using

        remdezivir is shutting down people’s kidneys and causing fluid to fill their lungs and then the high pressure ventilator they shove in them finishes them off by rupturing the remaining lungs tissues and another one bites the dust.

  2. I trust Old Bill Andrews some random guy much more that an award winning journalist that hasn’t sold out to the propaganda machine. There is a good possibility of the vaxed will die or have serious health problems over the next 3-5 years. Bill do some research on ADE, I guess the guy (Robert Malone) that created this technology doesn’t stand up to these genius TV doctors. This is what the doctors that have been black listed by the big tech/media have said since the beginning. THIS IS ONLY ABOUT CONTROL AND HAS NOTHING TO DO WITH HELPING MANKIND.

  3. So for every 300 people who get Covid, one dies. No doubt that one had other health problems or was over 80. That’s not even as bad as the common flu. It’s time for all of the terrified “Covidiots” to wake up and get over it!

  4. This data is similar to that of Israel’s, which is not surprising. The government health agencies of the UK and Israel are not corrupt as is the US. For a very long time the US was held up as the gold standard, not any more unfortunately. With the infiltration of activists and corrupt scientists (in name only) who either side with BIG Pharma or crooked politicians, the federal health agencies are currently nothing more than propaganda outlets for whatever government officials desire for the public to know, whether facts or lies/misinformation/disinformation will depend on what narrative they want to spin onto the public. And yet they wonder why the level of trust in them is so low.

      1. Posting links w/o any explanation or highlights is really just assigning homework that most of us will turn in late. Ms Attkisson is an award winning old school journalist and to challenge her report with just a pithy “not exactly” comment is vague and practically irrelevant in constructive debate. If you don’t mind share with The Great Unwashed exactly what is in her column that is not exactly right. I’ll wait.

      2. The one-shot vaccinated seem to be included with the unvaccinated in this data, muddying the results a bit. It would be nice if they completely separated out the unvaccinated data, as having even one vaccination doesn’t really mean you’re unvaccinated.

      3. Less than 1% of those infected would have become seriously ill had they been given any of tha at lesst half dozen EARLY treatments which includes Ivermectin…….NIH APPROVES Ivermectin as a treatment, along with several others….and provides High Value Studies from around the world, and USA, that backs that up.

        Discussion of cases, deaths, etc of CVD w/o concurrent treatment with Ivermectin, and similar drugs is meaningless.

        India proved this. READ

  5. I believe to throw data around without discussing which vax is a little misleading. There are four different vaccines being used in the UK, with Astra Zeneca being the most common. Not exactly the same efficacy as Moderna or Pfizer. The bottom line is who really knows what is happening with the vaccines and the Hippocratic oath of “first do no harm” should come into play when mandating vaccines even for those with natural immunity or who are at risk for serious complications from the vax. What about studies into the cessation of menstrual cycles of young women who have been vaccinated ? There is no one-size-fits-all solution.

    1. But in Israel, almost everyone got the Pfizer vaccine, so your argument does not hold water.
      There is no one-size-fits-all solution, but those of us who have been vaccinated, even though we are still vulnerable to the variants, have a much better chance of 1) survival; 2) staying away from a hospital; and having a much milder case of Covid-19 than if we were unvaccinated.

      1. Millions in India stay home, take Ivermection, and an area with 240 m people stopped CVD cold in one month, at a cost of about $1.80 per person.

      2. Yes, do provide proof of your statements Kenneth. Is it because fauci said so Kenneth? Plenty of evidence available to support the fact of cheap effective treatments being used and saving many lives ecen as they are being shoved to the side by many of our doctors here in the US because of money.

  6. Convid19 has been the largest scale crime ever perpetrated upon the people of the world. The volunteers of the mass vaccination campaign is proving to be a pandemic of mass stupidity…

  7. Sadly, even people who I consider intelligent simply skim through mainstream media and believe whatever they are told is truth with absolutely no documentation to back media’s claims. People in the U.S. have been dumbed down through the decades to leave politics to the few, not check any scientific data for themselves or think about how what is going on today will do to our children and grand-children. They would much rather spend their time watching dog and cat videos on you idiot tube or faceboob.

  8. Marc Maximilien Authier

    As with influenza, the covid 19 is a FRAUD. You cannot immunize anyone with a vaccine when a virus changes it genome every 24 hours. It is for this same reason that influenza vaccines never worked. But here it far more criminal. The spikes are indeed anti bodies but one vicious twist !!!! They are as pathogenic as the virus !!!!! In sum the virus is the vaccine and the vaccine is the virus. Both are interchangeable and provoke the same effect with an extra quicker called pathogenic priming or ADE antibody dependent enhancement. The more you will take more spikes the sicker and more infectious and infected you will become.

  9. Or they didn’t treat early with all the stuff that works like ivermectin, monoclonal antibodies, budesonide, zinc, d3, zpack or doxycycline and they went to the hospital were the prophet over health based protocols killed them.

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