Debt Rattle August 23 2021
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Didn’t Dr. McCullough say he welcomed approval so real tests could be done on the “vaccine”? They could actually take it apart and see what’s in it?
The ideal product produces addiction- something you don’t just want, but that you need.
Withholding is one of the best manipulative devices of all.Thanks to All-Y’all again today. My heart is happy to see your writings. Picture of me on the blog is not the one of me bending over and picking the squash.
That one was all butt, not flattering at all.
This one makes me look buff and sexy holding a fresh vegetable in the squash & banana patch
https://www.johndayblog.com/2021/08/consulted-more-fortunate-countries-of.htmlThe “more fortunate” countries of the world made the kind of deal with Pfizer last fall, that you or I might make with a mortgage lender, or when taking out a home-equity loan. The superior party bears no risk, and actually gains even more if the lesser party defaults. No way out, except to pay up.
Pfizer had good reason to exact such iron-clad contracts, which held Pfizer blameless in any circumstance which might arise. It’s good-business, of course, but the risks for antibody dependent enhancement (of viral pathogenicity) were well known, and no coronavirus vaccine studied had been successful in 20 years of trying.
The vaccinated animals made antibodies, but died at higher rates than the unvaccinated animals when challenged with viral infection.
Antibodies “against” a virus can turn out to be “for” the virus, to help it be more infectious.
That effect takes time to develop, like half a year to get started, in general.
There is evidence that is happening with vaccines against the original “alpha”-COVID spike protein now helping the Indian-originated delta-COVID have enhanced infectivity in vaccinated people.
That is just getting started, though, because it’s kind of accidental that delta-COVID can do a bit of this. Delta-COVID evolved in India with about 4% population vaccination, so it was just trying to spread effectively in a population. It did not have to dodge vaccine-created antibodies on the path to that success.
Now, in much of the world, like where we live, a majority of susceptible people have blocking-and-enhancing antibodies to alpha-COVID spike protein, due to vaccination. The viral mutations of resistance to blocking antibodies will be rewarded with more viral success in spread, but there is now a new option. Viral mutation to get more TURBO-BOOST out of the enhancing antibodies opens the door to new viral strains that will be more infectious to the vaccinated than to the unvaccinated.
This environmental niche has been created among spike-protein-vaccinated human hosts.
I suspect that mutant COVID variants yet-unnamed are already filling it.
Stay tuned, especially to Israel.I’ll break these up. They wouldn’t post together:
A scientific paper from Nature, last October, gives clear historical context regarding this common and devastating and difficult to avoid vaccination side effect.
Look, they got this problem when they tried to make vaccines for SARS-Co-V and MERS, the close cousins of our current COVID family.
In this Perspective, we summarize examples of vaccine-associated disease enhancement in the history of developing vaccines against respiratory syncytial virus, dengue virus, SARS-CoV and Middle East respiratory syndrome coronavirus, which highlight the importance of a robust safety and efficacy profile, and present recommendations for preclinical and clinical evaluation of COVID-19 vaccine candidates as well as for vaccine design and optimization.
https://www.nature.com/articles/s41579-020-00462-y Here is a specific mechanism of vaccine-antibodies to alpha-COVID spike protein enhancing the ability of delta-COVID to enter human cells, once the spike protein anchors to the cell. This is demonstrated to predominate in effet over the blocking antibodies, since delta mutated and they lost effectiveness against it.
Infection-enhancing anti-SARS-CoV-2 antibodies recognize both the original Wuhan/D614G strain and Delta variants. A potential risk for mass vaccination?
Using molecular modeling approaches, we show that enhancing antibodies have a higher affinity for Delta variants than for Wuhan/D614G NTDs. We show that enhancing antibodies reinforce the binding of the spike trimer to the host cell membrane by clamping the NTD to lipid raft microdomains. This stabilizing mechanism may facilitate the conformational change that induces the demasking of the receptor binding domain. As the NTD is also targeted by neutralizing antibodies, our data suggest that the balance between neutralizing and facilitating antibodies in vaccinated individuals is in favor of neutralization for the original Wuhan/D614G strain. However, in the case of the Delta variant, neutralizing antibodies have a decreased affinity for the spike protein, whereas facilitating antibodies display a strikingly increased affinity.
https://www.journalofinfection.com/article/S0163-4453(21)00392-3/fulltextPfizer coerced deals upon countries that desired to obtain it’s COVID-19 vaccines last year, which broke laws of those countries, could not be revoked under any conditions or in light of new information or treatments (ivermectin, deadly side effects), and in some cases gave Pfizer ownership of things like military bases, should the country default. Thanks Luc. It was a seller’s market. Israel got a deal.
In history’s largest medical experiment with “vaccines” that have not been approved for use in humans, it is the buyers’ responsibility to defend Pfizer for causing harm, leaked documents showed. Pfizer has escaped all liability and is indemnified, arguing that side effects and the long-term effects of the injections are unknown – to the company as well. Pfizer thus admits that an insufficiently tested product is being pushed in literally billions of doses on the world market.
This means that all responsibility for costs, healthcare, etc. due to vaccine damage – no matter how large and onerous – is passed on to the taxpayers in the countries that have signed the agreements. Since the agreements put each country’s own laws out of play, they have all been signed at government level.Bombshell leak: Countries that buy Pfizer’s vaccine undertake to break the law
(Ram it through quick!) British Medical Journal: Covid-19: FDA set to grant full approval to Pfizer vaccine without public discussion of data
Last year the FDA said it was “committed to use an advisory committee composed of independent experts to ensure deliberations about authorisation or licensure are transparent for the public.”1 But in a statement, the FDA told The BMJ that it did not believe a meeting was necessary ahead of the expected granting of full approval.
https://www.bmj.com/content/374/bmj.n2086 People have not been able to get doctors to prescribe ivermectin for COVID treatment and prevention, so they have bought veterinary ivermectin to use, mostly the horse-paste, but there are also some horse pills. A horse weighs about 10 times as much as a human, so people who take a horse pill, at 10X the human dose are getting nausea, vomiting, diarrhea and dizziness, but that’s all. No deaths, and the one “hospitalization” in Mississippi, does not appear to be confirmed. Take the right dose. If you can’t do math, get help from a farm-boy who can. These horse products are used on goats, rabbits, farmers and farmers children, at the correct scaling doses. Ask a farmer with critters. FDA resorts to shouting and public shaming, because it’s hard to fear safer-than-Tylenol ivermectin.
The FDA Is Begging You Not to Take Horse Dewormer for Covid-19
“You are not a horse. You are not a cow,” the Food and Drug Administration said about using the drug that hosts on Fox News have been pushingThe FDA Is Begging You Not to Take Horse Dewormer for Covid-19
American Journal of Therapeutics:
Moderate-certainty evidence finds that large reductions in COVID-19 deaths are possible using ivermectin. Using ivermectin early in the clinical course may reduce numbers progressing to severe disease. The apparent safety and low cost suggest that ivermectin is likely to have a significant impact on the SARS-CoV-2 pandemic globally.
https://journals.lww.com/americantherapeutics/fulltext/2021/08000/ivermectin_for_prevention_and_treatment_of.7.aspxComment from Denninger, someone had the stomach to read the FDA papers, and it looks like an extension of the EUA. Another bluff?
Some of the points myade by a senior editor of the British Medical Journal BMJ.
(Thanks to John Day for the link.)Does the FDA think these data justify the first full approval of a covid-19 vaccine?
August 23, 2021The elephant named “waning immunity”
…“Waning immunity” is a known problem for influenza vaccines, with some studies showing near zero effectiveness after just three months, meaning a vaccine taken early may ultimately provide no protection by the time “flu season” arrives some months later. If vaccine efficacy wanes over time, the crucial question becomes what level of effectiveness will the vaccine provide when a person is actually exposed to the virus? Unlike covid vaccines, influenza vaccine performance has always been judged over a full season, not a couple months.
And so the recent reports from Israel’s Ministry of Health caught my eye. In early July, they reported that efficacy against infection and symptomatic disease “fell to 64%.” By late July it had fallen to 39% where Delta is the dominant strain. This is very low. For context, the FDA’s expectation is of “at least 50%” efficacy for any approvable vaccine.Delta may not be responsible
Enter Pfizer’s preprint. As an RCT reporting “up to six months of follow-up,” it is notable that evidence of waning immunity was already visible in the data by the 13 March 2021 data cut-off… And it’s hard to imagine how the Delta variant could play a real role here, for 77% of trial participants were from the United States, where Delta was not established until months after data cut-off.
Waning efficacy has the potential to be far more than a minor inconvenience; it can dramatically change the risk-benefit calculus.The “six month” preprint based on the 7% of trial participants who remained blinded at six months
Despite the reference to “six month safety and efficacy” in the preprint’s title, the paper only reports on vaccine efficacy “up to six months,” but not from six months. This is not semantics, as it turns out only 7% of trial participants actually reached six months of blinded follow-up (“8% of BNT162b2 recipients and 6% of placebo recipients had ≥6 months follow-up post-dose 2.”) So despite this preprint appearing a year after the trial began, it provides no data on vaccine efficacy past six months, which is the period Israel says vaccine efficacy has dropped to 39%.
It is hard to imagine that the <10% of trial participants who remained blinded at six months (which presumably further dwindled after 13 March 2021) could constitute a reliable or valid sample to produce further findings.Severe disease
And on preventing death from covid-19, there are too few data to draw conclusions—a total of three covid-19 related deaths (one on vaccine, two on placebo). There were 29 total deaths during blinded follow-up (15 in the vaccine arm; 14 in placebo).
The crucial question, however, is whether the waning efficacy seen in the primary endpoint data also applies to the vaccine’s efficacy against severe disease. Unfortunately, Pfizer’s new preprint does not report the results in a way that allows for evaluating this question.Approval imminent without data transparency, or even an advisory committee meeting?
…But here we are, with FDA reportedly on the verge of granting a marketing license 13 months into the still ongoing, two year pivotal trial, with no reported data past 13 March 2021, unclear efficacy after six months due to unblinding, evidence of waning protection irrespective of the Delta variant, and limited reporting of safety data. (The preprint reports “decreased appetite, lethargy, asthenia, malaise, night sweats, and hyperhidrosis were new adverse events attributable to BNT162b2 not previously identified in earlier reports,” but provides no data tables showing the frequency of these, or other, adverse events.)
It’s not helping matters that FDA now says it won’t convene its advisory committee to discuss the data ahead of approving Pfizer’s vaccine. (Last August, to address vaccine hesitancy, the agency had “committed to use an advisory committee composed of independent experts to ensure deliberations about authorization or licensure are transparent for the public.”)Does the FDA think these data justify the first full approval of a covid-19 vaccine?
Didn’t Dr. McCullough say he welcomed approval so real tests could be done on the “vaccine”? They could actually take it apart and see what’s in it?
He thought there would be testing. There won’t be. Also not after the approval.
I saw that as well, and from what I gathered, the “approval” appears to be an extension of the EUA to include a generic version (biologic) of the Pfizer vaccine. Page 2 and Page 12:
https://www.fda.gov/media/150386/download
So yeah, a huge bluff if I’m reading this correctly.
“…it looks like an extension of the EUA. Another bluff?”
It looks like the FDA approved the BioNTech brand (identical product to the Pfizer shots, and the Pfizer shots can substitute for the approved brand, the FDA says), while the FDA is keeping the Pfizer shots under the EUA (my guess is to allow younger children to use it with an EUA, or quicker rollout of booster shots, instead of first requiring further studies for the licensed brand).
On August 23, 2021, FDA approved the biologics license application (BLA) submitted by BioNTech Manufacturing GmbH for COMIRNATY (COVID-19 Vaccine, mRNA) for active immunization to prevent COVID-19 caused by SARS-CoV-2 in individuals 16 years of age and older……the EUA will remain in place for the Pfizer-BioNTech COVID-19 vaccine for the previously-authorized indication and uses, and to authorize use of COMIRNATY (COVID-19 Vaccine, mRNA) under this EUA for certain uses that are not included in the approved BLA…
COMIRNATY (COVID-19 Vaccine, mRNA) is the same formulation as the PfizerBioNTech COVID-19 Vaccine and can be used interchangeably with the Pfizer-BioNTech COVID-19 Vaccine to provide the COVID-19 vaccination series…
Thanks, ct and Doc. I can read cogent technical documents all day, but stuff that is designed to obfuscate doesn’t hold my attention.
From the Pulitzer-prize winning site ProPublica (not quite an “anti-vaxxer” source of misinformation):
The CDC Only Tracks a Fraction of Breakthrough COVID-19 Infections, Even as Cases Surge
Meggan Ingram was fully vaccinated when she tested positive for COVID-19 early this month. The 37-year-old’s fever had spiked to 103 and her breath was coming in ragged bursts when an ambulance rushed her to an emergency room in Pasco, Washington, on Aug. 10. For three hours she was given oxygen and intravenous steroids, but she was ultimately sent home without being admitted.
Seven people in her house have now tested positive. Five were fully vaccinated and two of the children are too young to get a vaccine…
“It’s like saying we don’t count,” said Ingram after learning of the CDC’s policy change. COVID-19 roared through her household, yet it is unlikely any of those cases will show up in federal data because no one died or was admitted to a hospital.
“Local staff members at the U.S. Embassy in Kabul are “deeply disheartened” by U.S. evacuation efforts and have expressed a sense of betrayal and distrust in the U.S. government…”
Hahaha, did they run out of Red, White and Blue Kool Aid ? Betrayal by the US Regime? Distrust of the US Regime War criminals… it took them fearing their own asses to realize the US Regime is untrustworthy. Illegally invading another Nation that had nothing to do with 9/11, but was invaded because of 9/11- I hope they really get to know the Taliban now.
“If they ban you from their restaurants…”
Yep it’s happening here in Wa State now. Got reports last night that restaurants in Bellingham and Seattle are now asking for vax cards to enter… funny how a restaurant owner I know was vaxd and got covid.So if you are vaccinated and then get covid, do they take your vaccine card away?
The reason I’m reading it as a generic version is due to the fact I was on a biologic for humalog and lantus insulins while living in MD. A biologic license allows other companies to produce the exact manufacturing techniques as the original instead of replacing one of the ingredients that would preclude a copyright violation. But Doc could be correct in their interpretation of the document, and that’s my hedge.
But at this point, as another Denninger commenter noted, what difference would it really make? If da TV says it’s full approval, then it’s full approval to the masses.
Losing taste and smell is just something I would like to avoid if at all possible. Never mind all of the other long haul symptoms. So, I will take precautions to avoid those negative outcomes.
Do you think the millions of dead murdered by the US Regimes Illegal wars miss not being able to taste and smell? Are those illegal wars and crimes against humanity committed by the Government you look to for your personal protection mandated and justified in your confused hypocritical mind?
Have you filed a complaint against the US Govt for murdering healthy citizens across the globe ?
Have you filed a complaint against Fauci and Gates funding biological weapons research at Wuhan?
So you support Fort Detrick and the US Biological Weapons Research and the millions of dollars spent creating Biological weapons by the US Regime?Does your confused mind tell you those Wars and Murders are necessary and justified…the same confused mind that believes that masks that don’t protect you will protect you? Your same confused mind that thinks the Vaccine will prevent you from getting the covid engineered bio weapon which actually does not prevent you from infection?
Interesting name for the newly-approved COVID “vaccine”. Names are of significance, I think; and that’s a curious one. Variations of same, too: see “ISIS, ISIL, Islamic State; Al Quaeda and its “variants”, and the many, many other re-brandings in our enlightened, and super high-tech™ world.
“Confusion” reigns (by design, I’d say).
On a better note, some flowers unexpectedly bloomed in my tiny garden this weekend. Victory..
“A Biologics License Application, or BLA, is FDA’s standard “full approval” mechanism for biological products, including therapeutics and vaccines.”
What’s the Difference Between Vaccine Approval (BLA) and Authorization (EUA)?
What’s the Difference Between Vaccine Approval (BLA) and Authorization (EUA)?
Well the results are in: I have two types of antibodies! Double the fun. Anyways Karl D said don’t get an antibody test until two weeks after you stop showing symptoms. The nurse i spoke with at CVS confirmed this. So a week after i was showing for them, thats good. Negative test for covid and positive on the antibodies. If i could taste beer i’d go out and celebrate ;).
I found this piece when looking for more info on Malcolm Kyenune:
Which Side Are You On? The Answer is Clear for Today’s Useful Idiots for the Right
Not essential at all; but notable for its nastiness toward anyone suggesting solidarity toward others that aren’t just like you, for a Greater Good (a term that they’re working hard
to debase, as well). Reads like one of Our -IA friends’ work to me, actually..The light of Fall is beginning to show even though it’s still August, and I like that (no hidden meaning there, I just like that somehow-poignant slant best). Taking meaning where I can find it.
Re.: Central retinal vein occlusion
Doc feels that mine is the hardening of the veins due to old age.
No solution to fix.
Get injections once per month and laser to maybe help from getting worst.
The doc said, had one patient due to vaccine.Does the “Delta Strain” exist? How could one know?
Does a COVID hysteria exist? To that I can safely say “yes”, though I *still know of no one* who
become seriously ill or died, as a result of COVID. One anecdote.Zinc does seem to be better absorbed when taken with green tea, IME. I’ve been using the Jarrow
‘Zinc Balance’ because it has a little bit of copper in it.TDub: “We are continuously told that it is a “pandemic of the unvaccinated” with scary statistics like 99% of those in the hospital are unvaxxed. Does anyone have a source for that data?”
New York Magazine (clearly not an “anti-vaxxer source of misinformation”) examined those numbers and says they are distorted (“a closer look at the data reveals that some of the public-health communication may be overstating the vaccine effect on transmission and understating the scale and risk of breakthrough infections.” )
“The message that breakthrough cases are exceedingly rare and that you don’t have to worry about them if you’re vaccinated — that this is only an epidemic of the unvaccinated — that message is falling flat,” Harvard epidemiologist Michael Mina told me…
On Wednesday, a large pre-print study published by the Mayo clinic suggested the [vaccine] efficacy against infection had fallen as far as 42 percent.
“The breakthrough problem is much more concerning than what our public officials have transmitted,” Topol continued. “We have no good tracking. But every indicator I have suggests that there’s a lot more under the radar than is being told to the public so far, which is unfortunate.” The result, he said, was a widening gap between the messaging from public-health authorities and the meaning of the data emerging in real time. “I think the problem we have is people — whether it’s the CDC or the people that are doing the briefings — their big concern is, they just want to get vaccinations up. And they don’t want to punch any holes in the story about vaccines. But we can handle the truth. And that’s what we should be getting.”
The central distortion reflected in the Kaiser report — and echoed by communicators elsewhere, including in the Times — is the result of a basic error of comparison, one that should have been obvious to anyone familiar with the shape of the pandemic. Almost all of these calculations about the share of breakthrough cases have been made using year-to-date 2021 data, which include several months before mass vaccination (when by definition vanishingly few breakthrough cases could have occurred) during which time the vast majority of the year’s total cases and deaths took place (during the winter surge).This is a corollary to the reassuring principle you might’ve heard, over the last few weeks, that as vaccination levels grow we would expect the percentage of vaccinated cases will, too — the implication being that we shouldn’t worry too much over panicked headlines about the relative share of vaccinated cases in a state or ICU but instead focus on the absolute number of those cases in making a judgment about vaccine protection across a population. This is true. But it also means that when vaccination levels were very low, there were inevitably very few breakthrough cases, too. That means that to calculate a prevalence ratio for cases or deaths using the full year’s data requires you to effectively divide a numerator of four months of data by a denominator of seven months of data. And because those first few brutal months of the year were exceptional ones that do not reflect anything like the present state of vaccination or the disease, they throw off the ratios even further. Two-thirds of 2021 cases and 80 percent of deaths came before April 1, when only 15 percent of the country was fully vaccinated, which means calculating year-to-date ratios means possibly underestimating the prevalence of breakthrough cases by a factor of three and breakthrough deaths by a factor of five. And if the ratios are calculated using data sets that end before the Delta surge, as many have been, that adds an additional distortion, since both breakthrough cases and severe illness among the vaccinated appear to be significantly more common with this variant than with previous ones.
Unfortunately, more accurate month-to-month data is hard to assemble — because the CDC stopped tracking most breakthrough cases in early May, before the Delta wave had begun, and the states maintaining their own databases often update them irregularly and, in some cases, according to idiosyncratic logic..
Don’t Panic, But Breakthrough Cases May Be a Bigger Problem Than You’ve Been Told Current public-health messaging may understate the scale and risk.
https://nymag.com/intelligencer/2021/08/breakthrough-covid-19-cases-may-be-a-bigger-problem.html@Doc Robinson – thanks for that article. “Their big concern is, they just want to get vaccinations up. And they don’t want to punch any holes in the story about vaccines.”
If NY Magazine was able to review those numbers, does that mean they exist somewhere for the rest of us to see? A few similar comparisons from Israel have been shown on TAE before, would be nice to see the hard numbers that support the ‘pandemic in the unvaxxinated claim”
Just finished watching the Dellingpole/Miller interview: ding ding ding ding ding! Miller even mentions having just finished “That Hideous Strength”. I’ll have to find his donation page to help his lawsuit.
Git yer money off to the folks you love before it’s worthless!> ‘Don’t Panic, But Breakthrough Cases May Be a Bigger Problem Than You’ve Been Told’ <
Yes, more interesting messaging: “Don’t panic/please panic!!!”
And over at NC the “vaccine” approval didn’t seem to merit even a post. Odd..
also, the few worthy commenters there are no longer appearing; not sure if
they’re being “moderated”, or there other reasons.Looking forward to the days- maybe soon to come- when “messaging” will be a very bad word.
I just watched Catherine Austin-Fitts talking to Del Bigtree. A lot of similar information as in the Planet Lockdown video with her that I posted yesterday. I recommend you watch that, although this is quite good, too.
She explains about how everything is being set up for a move to a central bank digital currency (The Grim Reset) and the vaccine passports are an essential part of that which will allow full monitoring (and control) of everything you do and hence a social credit scheme. The lockdowns and the riots of last year were to trash small businesses and hand their real estate to the likes of Blackrock etc. The “vaccines” are to reduce life expectancy and hence solve the pension crisis, but you all already knew all that.
<iframe class=”rumble” width=”640″ height=”360″ src=”https://rumble.com/embed/vih7i3/?pub=4″ frameborder=”0″ allowfullscreen></iframe>
John Day: nice photo with the Squash. Looks like my Mom’s plot in the Central Valley circa 1975 or so.
Would’ve said said so on your blog but can’t seem to comment there. Lovely to see life coming out of
the ground.“Pandemic of the unvaccinated” is a phrase I’ve been reading a lot lately in MSM and official pronouncements.
Something seems off.Consider the following options:
1) “Pandemic among the unvaccinated”
2) “Pandemic in the unvaccinated”
3) “Pandemic of the unvaccinated”What solution(s) to the problem “pandemic” are implicitly suggested by each?
Why use the third?Jonathan Richman wrote and sang ‘Monologue About Bermuda’ (hope I got the exact title right).
It’s worth hearing, I think. He doesn’t use a compyooter. Kudos, JR!This part of the letter struck me as very strange though, and of course I know it’s designed to confuse:
“Conditions Related to Printed Matter, Advertising, and Promotion
X. All descriptive printed matter, advertising, and promotional material, relating to the
use of the Pfizer-BioNTech COVID‑19 Vaccine shall be consistent with the
authorized labeling, as well as the terms set forth in this EUA, and meet the
requirements set forth in section 502(a) and (n) of the FD&C Act and FDA
implementing regulations.Y. All descriptive printed matter, advertising, and promotional material relating to the
use of the Pfizer-BioNTech COVID‑19 Vaccine clearly and conspicuously shall state
that:• This product has not been approved or licensed by FDA, but has been
authorized for emergency use by FDA, under an EUA to prevent Coronavirus
Disease 2019 (COVID-19) for use in individuals 12 years of age and older; and• The emergency use of this product is only authorized for the duration of the
declaration that circumstances exist justifying the authorization of emergency
use of the medical product under Section 564(b)(1) of the FD&C Act unless the
declaration is terminated or authorization revoked sooner.”Seems strange they would include those qualifiers.
Hi Raul, A few days ago, I swear we saw a wonderful video about the vaccinations, featuring a young woman who was arguing with herself about why one should (should not) get a vaccination. She took on both the role of the person pushing the vaccines and the person asking perfectly reasonable questions about why it would even be advised, since it doesn’t work. When I go back to find that video (I believe it was originally from Tik Tok), I cannot find it. Could someone please post it again? I want to share it with others who feel as I do, that there is no logic to the argument that one should get the shot. Thank you for considering this request!
St Vincent’s hospital in Dublin is admitting a “worrying” number of double-vaccinated patients for treatment for Covid-19, emergency department head Professor John Ryan has said.
The authoritarian corporate state is fully in place in the West. The basic problem is that criminal taking of wealth only works as long as the crooks are allowed to leave devastation in their wake. Kabul fell because the Afghans fought back against the Imperialist imposed corrupt government.
The FDA approval of the marketing of “Comimaty” vaccine without a public hearing was done to avoid discussion of the known risks, unknown long-term risks, the vaccine’s failure to prevent transmission of the virus, and fading efficacy just months after injection. That this for-profit vaccine is the sole US governmental response to the Coronavirus Pandemic plus the rising death toll from the Delta Variant show utter incompetence. Only the restoration of democracy, good governance and the rule of law will avoid chaos and preserve civilization.
When the internet and TAE are silenced, recognize that this is a sign of the final death throes of global predatory capitalism.
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