If only he had been vaccinated

The daily Vaccine Nazi sob story is today focused on reasonable people who just want to wait for more scientific data instead of the usual anti-vaxxers:

Removal firm boss Brian Lynch, 46, said he was not an anti-vaxxer, but wanted more long-term scientific data before getting the jab.

He was admitted to Royal Blackburn Hospital on July 7 and spent weeks in intensive care, during which he vowed to friends he would get the vaccine if he recovered.

In a Facebook post from his ICU bed Mr Lynch said he felt ‘the most frightened he had ever been’ and admitted he ‘thought it was the vulnerable and the elderly who got hospitalised’.

But Mr Lynch, of Blackburn, Lancashire, was later placed in a medically-induced coma and died with his family and wife Gina by his side on July 31.

Mr Lynch’s death is the latest in a series of vaccine sceptics and anti-vaxxers who have died after refusing to receive the jab this year. 

The lesson: Don’t wait for the long-term scientific data! Get fully vaccinated now and you won’t… um, okay, well, wait a minute…. 

Sheriff Lee D. Vance died at his Jackson home on Wednesday, nearly two weeks after testing positive for COVID-19.

AMR responded to a medical emergency at Sherriff Vance’s home on Wednesday morning, according to a declaration issued by the Hinds County Sheriff’s Office. When the medical response team arrived, Vance did not respond and was pronounced dead.

Hinds County Sheriff Captain Tyree Jones confirmed the news to WLBT-TV this week. On August 4, the department Noted that Vance died of natural causes due to COVID-19, according to coroner Sharon Grisham-Stewart. His death will be labeled as a “COVID-related death.”

The sheriff was fully vaccinated and did not suffer an adverse effect, but despite his vaccinations and his age, contracted a lethal case of Covid-19. This appears to be ADE-in-action. 


Vaxx more dangerous than not being vaxxed

Scientists have known since December 2020 that the vaccines not only do not protect against the transmission of Covid-19 or reduce the severity of it, but actually make the vaccine recipients subject to more serious cases of the disease. 

Informed consent disclosure to vaccine trial subjects of risk of COVID‐19 vaccines worsening clinical disease

COVID‐19 vaccines designed to elicit neutralising antibodies may sensitise vaccine recipients to more severe disease than if they were not vaccinated. Vaccines for SARS, MERS and RSV have never been approved, and the data generated in the development and testing of these vaccines suggest a serious mechanistic concern: that vaccines designed empirically using the traditional approach (consisting of the unmodified or minimally modified coronavirus viral spike to elicit neutralising antibodies), be they composed of protein, viral vector, DNA or RNA and irrespective of delivery method, may worsen COVID‐19 disease via antibody‐dependent enhancement (ADE). This risk is sufficiently obscured in clinical trial protocols and consent forms for ongoing COVID‐19 vaccine trials that adequate patient comprehension of this risk is unlikely to occur, obviating truly informed consent by subjects in these trials.

Conclusions drawn from the study and clinical implications

The specific and significant COVID‐19 risk of ADE should have been and should be prominently and independently disclosed to research subjects currently in vaccine trials, as well as those being recruited for the trials and future patients after vaccine approval, in order to meet the medical ethics standard of patient comprehension for informed consent.

This is exactly what is happening now and explains why so many incidents of the spread of the disease being reported among completely vaccinated populations. Covid-19 is increasingly becoming a disease of the vaccinated due to Antibody-Dependent Enhancement. 

You can’t escape the experiment, so be the control group.

Your Vaccine Nazi friends and family may think they were sufficiently informed to consent to be vaccinated. They were not.

CONCLUSION

Given the strong evidence that ADE is a non‐theoretical and compelling risk for COVID‐19 vaccines and the “laundry list” nature of informed consents, disclosure of the specific risk of worsened COVID‐19 disease from vaccination calls for a specific, separate, informed consent form and demonstration of patient comprehension in order to meet medical ethics standards. The informed consent process for ongoing COVID‐19 vaccine trials does not appear to meet this standard. 



Bindery Campaign update 5

Days Left: 23

Status: 50.3 percent of goal.

The Iliad: 170/500

The Odyssey: 165/500  

First, thanks very much to everyone who has already backed this campaign and is making the next big step possible. Second, as requested, we will add two more ways to support the campaign next week, at more affordable $50 and $150 levels. Third, I will remind you that I am neither customer nor technical support and all attempts to pursue either through this blog or on the Darkstream will be deleted and ignored.

I understand that many organizations operate under the principle that “the customer is always right”. We absolutely do not. To the contrary, we operate under the principle that could be described as “the customer is probably retarded”. This is not to say we do not appreciate, respect, or hold in the highest regard everyone who supports our projects and makes them possible, but the negative baseline is necessary if we are to successfully anticipate even a small fraction of the customer-related problems that inevitably arise over time. Remember, MPAI.

For example, there is literally nothing we can do about a customer spamming our emails besides telling people – usually to no avail – to check their Social folders and whitelist our URLs. There is nothing we can do about a customer not giving us a shipping address, or moving without telling us that his address has changed. We cannot accept payment from an expired credit card. We cannot force anyone to read the emails that we send them. We are legally barred from contacting customers who intentionally remove themselves from our mailing list. (Believe it or not, one or two people do this almost every time we send out a mass email. Almost invariably, they later complain that we’re not keeping them informed.) These are the quotidian realities we face.

Moreover, until the bindery becomes operational, our ability to ensure that everyone gets their books in a reasonable timeframe is limited because we do not ship them to anyone. We literally never see them at all, and while our two primary partners have the best of intentions, both of them tend to fall short of the level of service that we consider to be acceptable. That is one of the primary reasons we are creating the bindery! In order to provide the level of service we wish to provide you, we have to control the entire process. And right now, we don’t, and unfortunately, neither of our partners are anywhere close to the Amazon level of operational performance and efficiency.

Now this doesn’t mean we aren’t 100-percent committed to ensuring that every single supporter and book buyer gets his books eventually, one way or another. For example, to address those who haven’t received the Junior Classics 1-3 hardcovers, the reason we aren’t losing any sleep about sorting out your problem right away is because you know we are going to be sending you books 4-6 this summer, and given our limited influence over the very large printing and distribution company that ships them, it is more effective to sort out each shipping problem with them once rather than addressing it multiple times. Trust us, we’ve been working with them for years, we know what works and what flat-out doesn’t.

As for what is taking so long to produce the Junior Classics, in addition to the editorial and layout processes, we are going through literally thousands of images, selecting hundreds of them, then carefully checking to make sure that they all work together aesthetically as well as with the related stories they illustrate. This takes time. This takes a LOT of time. Sure, we could have just taken the Easton approach, scanned the 1918 editions, and shipped all 10 volumes together six months ago, but that’s not what we do. 

I have the lovely two-volume Easton Press edition of The Tale of Genji. It is the exact same interior as my little octavo edition of the Waley translation I used in my Japanese literature course in college, scanned and blown up to royal octavo. And by “exact same”, I mean every typo and ink blot is perfectly replicated.

And I don’t believe that’s what our readers want. While we will use existing layouts for certain books in which the layouts cannot reasonably be improved – such as the Landmark history series, just to name one example for no particular reason at all – our standard modus operandi is to create new and unique layouts for each book in the Library.

I understand that some people would prefer that we provide gold-plated customer service. Since that’s not what we do at present, it would probably be better for such individuals to not do direct business with us, wait until the regular products are available through the mainstream channels, and pay the full retail price for them then. But it might be useful to reflect upon why so many of our customers are not meremly happy, but delighted with our products despite our horrific, bordering-on-nonexistent customer service.

We don’t spam, we don’t market (yet), we don’t even have an active dedicated Internet site at this point in time. All we do is make the highest-quality books that you can buy while systematically addressing one operational problem at a time. I very much hope that we can eventually reach the point where our customer service is as good as our interior layouts, but that is going to take at least two years, because it cannot be the priority at present. It will improve, just like the UATV technology is improving, but the process is intrinsically a gradual one that can be maddening at times.

Think about it. Are you really going to be happy with a gold-plated concierge service that calls you twice a day to inform you that your books are still not ready and you will not receive them today, tomorrow, or next week?


There is ZERO evidence of vaxx safety

The control group was vaccinated as soon as emergency authorization was granted

Mott was one of about 650 volunteers who took the experimental Moderna vaccine at a company called Johnson County Clinical Trials in Lenexa, Kan. Dr. Carlos Fierro, who runs the study there, says every participant was called back after the Food and Drug Administration authorized the vaccine.

“During that visit we discussed the options, which included staying in the study without the vaccine,” he says, “and amazingly there were people — a couple of people — who chose that.”

He suspects those individuals got spooked by rumors about the vaccine. But everybody else who had the placebo shot went ahead and got the actual vaccine. So now Fierro has essentially no comparison group left for the ongoing study.

“It’s a loss from a scientific standpoint, but given the circumstances I think it’s the right thing to do,” he says.

Be the control group. But don’t do it for yourself, or because you’re skeptical of an experimental product from a corporation granted legal immunity, or because you are concerned about the adverse effects of the vaxxes. 

Do it for science. 


Pfizer lied, people died

The Vaccine Nazis are now running around saying that the vaccines aren’t supposed to prevent infection, just serious illness and death. That is a blatant and easily disproven lie:

REAL-WORLD EVIDENCE CONFIRMS HIGH EFFECTIVENESS OF PFIZER-BIONTECH COVID-19 VACCINE AND PROFOUND PUBLIC HEALTH IMPACT OF VACCINATION ONE YEAR AFTER PANDEMIC DECLARED

Thursday, March 11, 2021 – 06:45am

Dramatically lower COVID-19 disease incidence rates observed in individuals fully vaccinated with the Pfizer-BioNTech vaccine, based on real-world data gathered by the Israel Ministry of Health  

Data suggest Pfizer-BioNTech vaccine prevents asymptomatic SARS-CoV-2 infection

Latest data analysis finds unvaccinated individuals were 44 times more likely to develop symptomatic COVID-19 and 29 times more likely to die from COVID-19

Findings represent the most comprehensive real-world evidence to date demonstrating the effectiveness of a COVID-19 vaccine

Read it again: “Data suggest Pfizer-BioNTech vaccine prevents asymptomatic SARS-CoV-2 infection”

And now the Vaccine Nazis are not only saying it isn’t preventing infections, they’re falsely claiming it isn’t even supposed to do so.


No vaccine regrets

It’s informative to see how the mainstream media avoids reporting on this sort of story. I suppose it’s hard to find the space with all the fake vaccine regret sob stories they’re running every day.

1st Vaccine done, absolutely zero side affects. Looking forward to 2nd one.

– Michael Mitchell, February 22, 2021

2nd vaccination done, zero after affect (as yet). Vaccine certificate issued.

– Michael Mitchell, March 20, 2021

Well that’s my third jab today. Proud to be part of this experiment to save lives.

– Michael Mitchell, July 16, 2021

Michael Mitchell was found dead in a marina cabin near his house boat on July 22, 2021.

Had a doctor been there, no doubt his last words would have been “vaccines are safe and effective.”