24 October 2021

Tommy Craig Power Play, Pt II, Also Fails

 So at the last BOC meeting JC Henderson once again attempted to interject caustic, former county attorney - Wm Thomas "Tommy" Craig, Esq, - into the body politic of the home county. 

Once again, it failed. 

The situation was as follows. 

Funds from the American Rescue Plan Act have been on the forefront of the minds of many, especially BOC 3 Rep Alana Sanders. In fact, she got state rep Sharon Henderson to address the BOC a while back in order to convince the county to release these funds into Sanders' control because - paraphrasing - a woman know how to get it done! 

BOC 3 Commissioner Alana Sanders

Fast forward to this past Tuesday & JC Henderson threw up his second Hail Mary in as many weeks & made a motion to allocate $10 million of these funds to be distributed by whom?

You guessed it. The one & only Tommy Craig. 

Once again, Henderson ended up withdrawing his motion. 

At this point, I think Tommy's like Gollum.

He's got the old office on College Ave fixed up real nice & apparently he's at least sort of fixed things up w/ the IRS (#thanksEzell) but seemingly that's not enough. 

He needs his Precious! 

He needs more of your tax money. 

And for the record, I think he kinda looks like him.  

Just another day in the home county, folks. 

- MBM 

P.S. Apparently the official minutes of the Newton BOC meetings do NOT include motions that are withdrawn. 

P.P.S. Alana Sanders = JC Henderson = Tommy Craig   

18 October 2021

Play Stupid Games, Win Stupid Prizes: JC Henderson Strikes Again

 From our friends at Citizens for a Better Newton

Thanks to Commissioner Henderson's shenanigans at a recent BOC meeting, a local property owner has withdrawn his planned donation of 4 acres of future park land and a 111 year old home to the county. A news article in this weekend's Covington News gives the details, but does not fully describe how Henderson hindered the donation by his actions and erroneous statements.
Henderson claimed at the BOC meeting that he wasn't involved in negotiating the conditions for the donation and therefore moved to table the motion to accept the land until he could get more involved and meet with the landowner. Both Chairman Banes and County Manager Kerr disputed Henderson's claim about his not being involved. They indicated that Henderson had been fully involved in meetings with the donor which apparently began in 2015. His motion to table the donation must have frustrated the landowner and in effect cost the citizens of his district a property worth over $100,000. That possibility was part of the discussion before Commissioner Sanders seconded the motion and it passed.
Without this donation, there appears to be no access from Brown Bridge Road to a future park site owned by the county (see photo below). Now, the only access will be through a subdivision which will be very unpopular with those homeowners.
Mr. Henderson must have not heard the old warning not to look a gift horse in the mouth. His constituents and others in West Newton are now the losers.


This is what happens when you let the inmates run the asylum.
Many, yours truly included, have been warning about JC for years, if not for decades.
Play stupid games & you'll likely win stupid prizes.


12 October 2021

Ellis Millsaps: Backtalk

 Glad to see that with his October 6 post MBM is back to talking about something he knows something about because his previous” Spartacus” post, aside from being nonsense, borders on being dangerous nonsense.

 What's wrong with Spartacus and those who channel it?

1) He, she or it is anonymous. If you are one who is filled with all this medical/ scientific knowledge that proves that everything we know is wrong, why wouldn't you want your name on it? Afraid of losing some job? The Nobel Prize for medicine would more than cover that. I will not be surprised if we learn that this is a Russian misinformation scam.

2) The website Marshall doesn't give you because it eviscerates Sparty is newswise.com. Check it out. It's notable that this is the only reputable site that even bothers to give such nonsense the dignity of a rebuttal. If you want credible information on covid go to WebMD. They are knowledgeable people who have no political slant I can see.

3)  Neither Sparty nor Marshall mention that over 90% of covid hospital admissions and nearly all of the deaths are unvaccinated people. This is a fact. If you don't recognize this it's because for perverse political reasons you don't want to. (Ed. note: source?)

4)  Marshall's “multitude of young people” with serious reactions to the vaccine are 4% of teenage boys. The reaction is a quite serious swelling of the heart which they are six times more likely to experience if they contract covid. Again, check it out at WebMD.

5)  MBM and his anonymous buddy say that natural immunity is more effective than vaccination. Well, duh, we suspected this for a long time before it's confirmation by an Israeli study. But Marshall and Sparty fail to mention that the only way you can get natural immunity is by living through a covid infection. It falls under the” kids don't try this at home” heading. Again, covid is way more likely to kill you or give you lingering debilities than the usually non-existent or minor reactions to the vaccinations.

 I say this stuff is potentially dangerous but I suspect that the vast majority of people who purport to believe this nonsense already believed it and we're just waiting for more conspiracy bullshit to confirm them. Remember, to work for Fox News you are mandated to be vaccinated or have daily testing done.  Fox, the source of much antivax propaganda, imposed this mandate before the president recommended it. 

- Ellis Millsaps

09 October 2021

JC Henderson's Full Motion To Bring Back Tommy Craig

 Here's the actual motion that JC Henderson tendered (and later withdrew after he saw it wasn't going to pass) to try to bring the former caustic attorney back. 

I'm sure Tommy wrote it up for JC. 

Again, and maybe I'm wrong, but I think this looks like an act of desperation. If they didn't have the votes, seems as if this was kind of a Hail Mary. 

We'll be keeping an eye on it. 

- MBM 

08 October 2021

The Home County Now Truly Dysfunctional

JC & Alana tryna act like they own the home county now (particularly, the line from JC from about ten months ago  -- " I own Newton County now, [expletive deleted]"). 


And it seems as if William Thomas (Wm Thomas) "Tommy Craig" / WTC is desperate. 

I was very surprised but heartened to see the recent developments. 

He's starting to get old though now, isn't he? 

Tell you what, though, all that money Ezell's been feeding him did help that sumbitch to keep the old office on College Ave from falling apart. 


Newton Co can't even take of its basic services anymore. 

Not surprising given the recent developments. 


The Tax Commissioner's office? 

We're seeing that falling apart in real-time, aren't we? 


The Sheriff's Department? 

It's been a mess for over a decade. 


What we recently saw w/ the Coroner's office w/ Madam Coroner? 


- MBM 

06 October 2021

Newton REAL Politick: Tommy Craig Power Play Put on Hold -- For Now...

 Hello readers, 

You can get the recap of the most recent developments w/ this over at the home county's legal organ

The mood of the current state of politics in the home county has been similar to the weather the last couple of days -- very dreary. 

A power play & a conspiracy - six years in the making - is now playing out right before our very eyes. 

Wm Thomas "Tommy" Craig wants that power, influence & money again. He's hungry for it & he can almost taste it. 

WTC -- The Million Dollar Man

The hundreds of thousands he's gotten from the Sheriff's Department every year the last few years has been chump change to him. No, he wants to start getting closer to a million per year again. 

Ever since his unceremonious bouncing out in the fall of 2015, he - as well as his main co-conspirator, BOC 4 Rep JC Henderson, and others - has been working towards this moment in time. 

JC channeling his best Don Fanucci: 
"You should let me wet my beak a little..."

For the moment, it didn't work...

We now know the lay of the land, however, and as we all already knew, BOC 3 Rep Alana Sanders is fully on board w/ Team WTC/JC (based on our sources, Craig was key to Sanders' run). 

We are fortunate that we have a wildcard right now. BOC 2 Rep Demond Mason, make no doubt about it, is the most powerful politician in Newton Co. right now. He's the key. He is NOT Team Craig, as far as we can tell. 

What was disturbing was the fact that BOC 5 Rep Ronnie Cowan publicly stated that the argument for bringing Craig on board as an assistant attorney had "merit."  That is easily the most concerning thing I've ever heard him say (and as many of you know, that's really saying something). Is Ronnie smoking Crack? WTF!? 

Lost in the shuffle of all of this is the fact that an extremely qualified attorney & good person that really loves Covington & Newton Co. - Ms Megan Martin - is being tossed around like a political rag dog due to dirty politics & likely just some good old fashioned racism. 

This is a very dark & sad time for the home county indeed. 

I'm hoping that a rabbit can be pulled out of the hat & a good ending will happen here but I'm quite doubtful of that at this moment. 

Frustrated & Disappointed, 

- MBM 

04 October 2021

Thoughts of the Current State of Things Related to the "Thing" & Excerpts from the Letter from "Sparty"

 Hello all. 

So things, at least from my vantage point, have gotten kind of quiet regarding the Co.V.id Nineteen. 

I wonder if this has anything to do w/ the multiple reports now emerging of the multitude of younger persons having serious adverse reactions to the non-traditional m-RNA "vaccine." 

Perhaps it has to do w/ the growing number of reports, studies & data clearly showing that natural immunity is way more effective than the aforementioned jabs. 

Maybe it's because more & more of the legacy media is no longer carrying water for the official narrative as it's becoming obvious, even to some of the most fervent "trust the science" supporters, that things just aren't adding up. 

Is the recent mass firings of medical personnel, those who've been on the front line of this thing since day one, who are now coming forward publicly w/ accounts of data manipulation & under-reporting of the SAERS system playing a role & that the numbers are now suggesting that the "not-a-vaccine" is harming & killing more folks under the age of 40 than the virus is. 

To all of those questions, comes the now infamous "Letter From Spartacus." 

Now, in full disclosure, I think this anonymous person (or most likely a group of people, who obviously have at least some advanced knowledge of diseases & medical treatments) really undercut their potential sphere of influence by getting into speculation & some questionable theories towards the latter end of their treatise, but its effect is now basically indisputable. As soon as several platforms started disappearing this incredible writing, it was going to ensure that it would get major traction; which, it has, likely to the tune of millions of views from thousands of different websites. 

To me, this seems like a legitimate paradigm shift. 

In particular, the following spoke volumes to me -- that one left-leaning website (which I will not be mentioning or linking to) did a critique on the piece & basically found just a handful of disputed facts out of the dozens & dozens of things mentioned by this piece. 

As I write this, I see Facebook is still down, not for pushing, what, six hours? And I have to wonder if this is all related? Maybe not. Maybe so. 

Very interesting times... 

W/out any further ado, here are excerpts from the Letter From Spartacus: 


• 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.

COVID-19 Transmission:

COVID-19 is airborne. The WHO carried water for China by claiming that the virus was only droplet- borne. Our own CDC absurdly claimed that it was mostly transmitted by fomite-to-face contact, which, given its rapid spread from Wuhan to the rest of the world, would have been physically impossible.

The ridiculous belief in fomite-to-face being a primary mode of transmission led to the use of surface disinfection protocols that wasted time, energy, productivity, and disinfectant.

The 6-foot guidelines are absolutely useless. The minimum safe distance to protect oneself from an aerosolized virus is to be 15+ feet away from an infected person, no closer. Realistically, no public transit is safe.

Surgical masks do not protect you from aerosols. The virus is too small and the filter media has too large of gaps to filter it out. They may catch respiratory droplets and keep the virus from being expelled by someone who is sick, but they do not filter a cloud of infectious aerosols if someone were to walk into said cloud.

The minimum level of protection against this virus is quite literally a P100 respirator, a PAPR/CAPR, or a 40mm NATO CBRN respirator, ideally paired with a full-body tyvek or tychem suit, gloves, and booties, with all the holes and gaps taped.

Live SARS-CoV-2 may potentially be detected in sewage outflows, and there may be oral-fecal transmission. During the SARS outbreak in 2003, in the Amoy Gardens incident, hundreds of people were infected by aerosolized fecal matter rising from floor drains in their apartments.

COVID-19 Vaccine Dangers:

The vaccines for COVID-19 are not sterilizing and do not prevent infection or transmission. They are “leaky” vaccines. This means they remove the evolutionary pressure on the virus to become less lethal. It also means that the vaccinated are perfect carriers. In other words, those who are vaccinated are a threat to the unvaccinated, not the other way around.

All of the COVID-19 vaccines currently in use have undergone minimal testing, with highly accelerated clinical trials. Though they appear to limit severe illness, the long-term safety profile of these vaccines remains unknown.

Some of these so-called “vaccines” utilize an untested new technology that has never been used in vaccines before. Traditional vaccines use weakened or killed virus to stimulate an immune response. The Moderna and Pfizer-BioNTech vaccines do not. They are purported to consist of an intramuscular shot containing a suspension of lipid nanoparticles filled with messenger RNA. The way they generate an immune response is by fusing with cells in a vaccine recipient’s shoulder, undergoing endocytosis, releasing their mRNA cargo into those cells, and then utilizing the ribosomes in those cells to synthesize modified SARS-CoV-2 Spike proteins in-situ.

These modified Spike proteins then migrate to the surface of the cell, where they are anchored in place by a transmembrane domain. The adaptive immune system detects the non-human viral protein being expressed by these cells, and then forms antibodies against that protein. This is purported to confer protection against the virus, by training the adaptive immune system to recognize and produce antibodies against the Spike on the actual virus. The J&J and AstraZeneca vaccines do something similar, but use an adenovirus vector for genetic material delivery instead of a lipid nanoparticle. These vaccines were produced or validated with the aid of fetal cell lines HEK-293 and PER.C6, which people with certain religious convictions may object strongly to.

SARS-CoV-2 Spike is a highly pathogenic protein on its own. It is impossible to overstate the danger presented by introducing this protein into the human body.

It is claimed by vaccine manufacturers that the vaccine remains in cells in the shoulder, and that SARS- CoV-2 Spike produced and expressed by these cells from the vaccine’s genetic material is harmless and inert, thanks to the insertion of prolines in the Spike sequence to stabilize it in the prefusion conformation, preventing the Spike from becoming active and fusing with other cells. However, a pharmacokinetic study from Japan showed that the lipid nanoparticles and mRNA from the Pfizer vaccine did not stay in the shoulder, and in fact bioaccumulated in many different organs, including the reproductive organs and adrenal glands, meaning that modified Spike is being expressed quite literally all over the place. These lipid nanoparticles may trigger anaphylaxis in an unlucky few, but far more concerning is the unregulated expression of Spike in various somatic cell lines far from the injection site and the unknown consequences of that.

Messenger RNA is normally consumed right after it is produced in the body, being translated into a protein by a ribosome. COVID-19 vaccine mRNA is produced outside the body, long before a ribosome translates it. In the meantime, it could accumulate damage if inadequately preserved. When a ribosome attempts to translate a damaged strand of mRNA, it can become stalled. When this happens, the ribosome becomes useless for translating proteins because it now has a piece of mRNA stuck in it, like a lace card in an old punch card reader. The whole thing has to be cleaned up and new ribosomes synthesized to replace it. In cells with low ribosome turnover, like nerve cells, this can lead to reduced protein synthesis, cytopathic effects, and neuropathies.

Certain proteins, including SARS-CoV-2 Spike, have proteolytic cleavage sites that are basically like little dotted lines that say “cut here”, which attract a living organism’s own proteases (essentially, molecular scissors) to cut them. There is a possibility that S1 may be proteolytically cleaved from S2, causing active S1 to float away into the bloodstream while leaving the S2 “stalk” embedded in the membrane of the cell that expressed the protein.

SARS-CoV-2 Spike has a Superantigenic region (SAg), which may promote extreme inflammation.

Anti-Spike antibodies were found in one study to function as autoantibodies and attack the body’s own cells. Those who have been immunized with COVID-19 vaccines have developed blood clots, myocarditis, Guillain-Barre Syndrome, Bell’s Palsy, and multiple sclerosis flares, indicating that the vaccine promotes autoimmune reactions against healthy tissue.

SARS-CoV-2 Spike does not only bind to ACE2. It was suspected to have regions that bind to basigin, integrins, neuropilin-1, and bacterial lipopolysaccharides as well. SARS-CoV-2 Spike, on its own, can potentially bind any of these things and act as a ligand for them, triggering unspecified and likely highly inflammatory cellular activity.

SARS-CoV-2 Spike contains an unusual PRRA insert that forms a furin cleavage site. Furin is a ubiquitous human protease, making this an ideal property for the Spike to have, giving it a high degree of cell tropism. No wild-type SARS-like coronaviruses related to SARS-CoV-2 possess this feature, making it highly suspicious, and perhaps a sign of human tampering.

SARS-CoV-2 Spike has a prion-like domain that enhances its infectiousness.

The Spike S1 RBD may bind to heparin-binding proteins and promote amyloid aggregation. In humans, this could lead to Parkinson’s, Lewy Body Dementia, premature Alzheimer’s, or various other neurodegenerative diseases. This is very concerning because SARS-CoV-2 S1 is capable of injuring and penetrating the blood-brain barrier and entering the brain. It is also capable of increasing the permeability of the blood-brain barrier to other molecules.

SARS-CoV-2, like other betacoronaviruses, may have Dengue-like ADE, or antibody-dependent enhancement of disease. For those who aren’t aware, some viruses, including betacoronaviruses, have a feature called ADE. There is also something called Original Antigenic Sin, which is the observation that the body prefers to produce antibodies based on previously-encountered strains of a virus over newly- encountered ones.

In ADE, antibodies from a previous infection become non-neutralizing due to mutations in the virus’s proteins. These non-neutralizing antibodies then act as trojan horses, allowing live, active virus to be pulled into macrophages through their Fc receptor pathways, allowing the virus to infect immune cells that it would not have been able to infect before. This has been known to happen with Dengue Fever; when someone gets sick with Dengue, recovers, and then contracts a different strain, they can get very, very ill.

If someone is vaccinated with mRNA based on the Spike from the initial Wuhan strain of SARS-CoV-2, and then they become infected with a future, mutated strain of the virus, they may become severely ill. In other words, it is possible for vaccines to sensitize someone to disease.

There is a precedent for this in recent history. Sanofi’s Dengvaxia vaccine for Dengue failed because it caused immune sensitization in people whose immune systems were Dengue-naive.

In mice immunized against SARS-CoV and challenged with the virus, a close relative of SARS-CoV-2, they developed immune sensitization, Th2 immunopathology, and eosinophil infiltration in their lungs.

We have been told that SARS-CoV-2 mRNA vaccines cannot be integrated into the human genome, because messenger RNA cannot be turned back into DNA. This is false. There are elements in human cells called LINE-1 retrotransposons, which can indeed integrate mRNA into a human genome by endogenous reverse transcription. Because the mRNA used in the vaccines is stabilized, it hangs around in cells longer, increasing the chances for this to happen. If the gene for SARS-CoV-2 Spike is integrated into a portion of the genome that is not silent and actually expresses a protein, it is possible that people who take this vaccine may continuously express SARS-CoV-2 Spike from their somatic cells for the rest of their lives.

By inoculating people with a vaccine that causes their bodies to produce Spike in-situ, they are being inoculated with a pathogenic protein. A toxin that may cause long-term inflammation, heart problems, and a raised risk of cancers. In the long-term, it may also potentially lead to premature neurodegenerative disease.

Absolutely nobody should be compelled to take this vaccine under any circumstances, and in actual fact, the vaccination campaign must be stopped immediately.