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- Jun 28, 2019
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Listen buddy, natural immunity and cross-immunity to related pathogens are a right-wing conspiracy, mkay?
The only Safe and Effective (TM) way to protect yourself and your community from Smallpox is the FDA-approved Pfizer mRNA Smallpox Vaccine. Find vaccines near you at healfkare.guv!
If there is a 'smallpox pandemic' as per the schizoidposts, then I do expect some mutant version of smallpox to be introduced to the public, just like how the coronavirus looks to have originated from a lab.Smallpox is a nothingburger. It doesnt mutate like coof and vaccines that have been proven over 100+ years are readily available...its a non story. Same with bird-flu..the traditional vaccines are literally ready for it.
Covid however mutates a bit much. Vaccination is pointless.
Anybody thinking smallpox or bird flu is a big deal is exceptional. It doesnt mutate.
If there is a 'smallpox pandemic' as per the schizoidposts, then I do expect some mutant version of smallpox to be introduced to the public, just like how the coronavirus looks to have originated from a lab.
While this nu-smallpox won't mutate as quickly as coronaviruses, the new vaccines for it also won't be in the hands of the public.
Well there is that case of the Spiegel journalist getting caught red-handed outright fabricating testimonies from alleged Syrians some years ago.
How are they even handling that? I can't imagine how much that would hurt.I went all through 2020 without knowing anyone whose significant other or anyone close to them "died suddenly and unexpectedly." Now it's happening multiple times in a week, and another friend's husband died suddenly in a similar age bracket in the week before.
Admittedly, anyone born after like 1980 globally or what, 1970 in the US has not had the small pox vaccine or any exposure. Well, I did meet a girl once who had cowpox. The rest of us in that age range would be naive, so we would have to go get that shot, if they are even still produced since we erradicated that.Smallpox is a nothingburger. It doesnt mutate like coof and vaccines that have been proven over 100+ years are readily available...its a non story. Same with bird-flu..the traditional vaccines are literally ready for it.
Covid however mutates a bit much. Vaccination is pointless.
Anybody thinking smallpox or bird flu is a big deal is exceptional. It doesnt mutate.
@chiobu
You should also post the actual document that mentions the 55 years.
Archived here: https://archive.md/9gKmh
<snip>
Well, as the on-screen text at the end of an episode of my favorite series once read: "To Be Continued".
Not suspicious at all ..
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FDA Asks Federal Judge For Permission to Withhold Pfizer COVID-19 Jab Data Until 2076 - NWT
Share The Story While that headline seems like clickbait, it’s a legitimate request the FDA made to a federal judge. The federal agency wants to withhold the full disclosure of the data and information of Pfizer’s COVID-19 injection for 55 years. Yet, they have no qualms approving the...newzworldtoday.com
"While that headline seems like clickbait, it’s a legitimate request the FDA made to a federal judge.
The federal agency wants to withhold the full disclosure of the data and information of Pfizer’s COVID-19 injection for 55 years."
A processing schedule is necessary because many different types of information are exempt from the FOIA, such that the government must redact that information before providing responsive records to the plaintiff. See 5 U.S.C. § 552(b)(1)–(b)(9). Reviewing and redacting records for exempt information is a time-consuming process that often requires government information specialists to review each page line-by-line. When a party requests a large amount of records, like Plaintiff did here, courts typically set a schedule whereby the processing and production of the non-exempt portions of records is made on a rolling basis.
In this case, FDA has assessed that there are more than 329,000 pages potentially responsive to Plaintiff’s FOIA request. (This page count is under-inclusive of the material responsive to the request, as it does not include certain types of records that cannot be meaningfully paginated, such as data captured in spreadsheets that contain thousands of rows of data.) The parties have conferred in good faith concerning a processing schedule, but have been unable to reach agreement for the reasons set forth in the parties’ Joint Report. See ECF No. 18.
After the December 1 production, FDA proposes to work through the list of documents that Plaintiff requested FDA prioritize for production in order of priority and process and release the non-exempt portions of those records to Plaintiff on a rolling basis. FDA proposes to process and produce the non-exempt portions of responsive records at a rate of 500 pages per month. This rate is consistent with processing schedules entered by courts across the country in FOIA cases.3
Plaintiff’s request (as set forth below) that FDA process and produce the non-exempt portions of more than 329,000 pages in four months would force FDA to process more than 80,000 pages per month. Undersigned counsel is not aware of any court ever granting such a request.
To ensure protection of this information, and other information subject to withholding under the FOIA exemptions, FDA must carefully review and, if necessary, redact exempt information on a line-by-line basis.
Second, the FDA does not have the personnel or resources in its FOIA office to process Plaintiff’s FOIA request at a rate of more than 80,000 pages per month.
The Branch has a total of ten employees, including the director and two trainees.
Moreover, FDA’s FOIA office does not have nearly the same level of personnel or resources dedicated to process FOIA requests as FDA has marshaled to review license applications for live-saving products in the middle of a pandemic.
It adequately balances the interests of the Plaintiff in responsive records with the interests of the vaccine sponsor in the protection of its confidential information, the interests of clinical trial participants in the protection of their personal privacy information, and the interests of other FOIA requesters whose requests are being processed alongside Plaintiff’s.
The FDA has proposed to produce 500 pages per month which, based on its calculated number of pages, would mean it would complete its production in nearly 55 years – the year 2076. Until the entire body of documents provided by Pfizer to the FDA are made available, anappropriate analysis by the independent scientists that are members of Plaintiff is not possible. Would the FDA agree to review and license this product without all the documents? Of course not.
It took the FDA precisely 108 days from when Pfizer started producing the records for licensure on May 7, 2021,14 to when the product was licensed on August 23, 2021. We assume, as the FDA has stated, that it conducted an intense, robust, thorough and complete review and analysis of those documents in order to assure that the Pfizer vaccine was safe and effective for licensure.
Plaintiff respectfully requests that the Court enter an order requiring the FDA to produce all documents and data submitted by Pfizer on a rolling basis such that all of it shall be produced on or before March 3, 2022, which is 108 days from today. To require less is to render FOIA meaningless, the FDA’s promise of transparency a lie, and to send a signal to every American that while the federal executive branch is shielding Pfizer from any liability for injuries from its product and requiring employers, schools, hospitals and the military to expel those that don’t receive this product, it is protecting the very documents Pfizer provided to our taxpayer-funded health agency
to obtain licensure to be able to sell this product.
Variola major has a death rate of 10-30%. That's 1 in 10 to 3 in 10 people dead.Smallpox is a nothingburger.
Mutation isn't inherently a negative, dumbass. If anything its a positive, since it accelerates viral evolution, which favors less lethal and more transmissible traits.Anybody thinking smallpox or bird flu is a big deal is exceptional. It doesnt mutate.
VIENNA, Nov 18 (Reuters) - Pressure on Austria's government to impose a full COVID-19 lockdown grew on Thursday as its worst-hit provinces said they would adopt the measure for themselves since infections are still rising despite the current lockdown for the unvaccinated.
Roughly 66% of Austria's population is fully vaccinated, one of the lowest rates in western Europe. Its infections are among the highest on the continent, with a seven-day incidence of 971.5 per 100,000 people.
Welcome to the last year.![]()
Austria's focus shifts to full lockdown as COVID-19 cases keep rising
Pressure on Austria's government to impose a full COVID-19 lockdown grew on Thursday as its worst-hit provinces said they would adopt the measure for themselves since infections are still rising despite the current lockdown for the unvaccinated.www.reuters.com
65% isn't low it's higher than the US and about the same as the UK. Other places with higher rates are jabbing 12+ children.
Anyway they've been keeping purbloods under house arrest for a week and this is the result.
View attachment 2730447
Speculation was that separating mudbloods and purebloods would only accelerate viral transmission, due to the maladapted immune response in the vaccinated. Speculation has become reality.
Austrian politics is a mess. They had a right wing coalition toppled because a pro immigration Iranian orchestrated a sting operation where the leaders of the coalition partner party said they would be willing to LEGALLY reward a russian oligarch for funding a anti islam campaign.![]()
Austria's focus shifts to full lockdown as COVID-19 cases keep rising
Pressure on Austria's government to impose a full COVID-19 lockdown grew on Thursday as its worst-hit provinces said they would adopt the measure for themselves since infections are still rising despite the current lockdown for the unvaccinated.www.reuters.com
65% isn't low it's higher than the US and about the same as the UK. Other places with higher rates are jabbing 12+ children.
Anyway they've been keeping purbloods under house arrest for a week and this is the result.
View attachment 2730447
Speculation was that separating mudbloods and purebloods would only accelerate viral transmission, due to the maladapted immune response in the vaccinated. Speculation has become reality.
I am not sad at all that those Austrian fuckers who thought it was fine and dandy to put 1/3 of the population under house arrest could soon be experiencing the sweet sensation of the boot on their collaborating necks.Austrian politics is a mess. They had a right wing coalition toppled because a pro immigration Iranian orchestrated a sting operation where the leaders of the coalition partner party said they would be willing to LEGALLY reward a russian oligarch for funding a anti islam campaign.
They then did the whole Trump saga thing where the Stasi knocked down doors and confiscated electronic communication to get them on charges not related to the Russian conspiracy that started the investigation.
And now the new coalition partner is the green party who would likely slit the throats of every white person in Europe if given the opportunity
Maybe im stupid here but can someone explain ti me how were they able to read, digest, understand and made the decision about all this Pfizer documents within a year but are unable to just submit them to the public and needs 50 years to do?@chiobu
You should also post the actual document that mentions the 55 years.
Archived here: https://archive.md/9gKmh
Take from the website of Siri Glimstad, the law firm which is operating on behalf of that group of scientists for transparency.
It's an ongoing legal battle, it seems.
These are the arguments of the FDA for refusing to immediately release all the Pfizer data they based their decision on:
- It's a 329'000 page document, and the FDA FOIA department (who are in charge of releasing requested data to the public) is staffed by 10 people and currently have a backlog of 400 other FOIA requests.
- They asked the plaintiffs to narrow down their request to more specific records, but apparently the plaintiffs refused to do so.
- Thus the FDA will only be able to release the data at a rate of 500 pages a month (@Virgo), so that the last batch will be released sometime in the year 2076. Aha! I hear you say, surely there'll be already enough juicy stuff popping up much earlier than that since they're not actually withholding the whole data until 2076. But a proper independent evaluation of this data is not appropriate until the whole set of 329'000 pages is released, rendering the partial dataset released earlier technically useless. Probably because the very last page of the mammoth document that they decide to release in 2076 contains a notary approved statement that "Everything in the previous 328'999 pages was a lie lololol I was only pretending to be exceptional".
Now the counterargument is based on two points:
- The FDA still managed to assess this gigantic 329k page document in 108 days (time elapsed between Pfizer's release of the data and the FDA's approval in mid-August 2021). Now it takes them 55 years to process it for public release?
- The FDA was well aware of the public interest surrounding this case and should have been prepared for a request of data release by concerned citizens,
Well, as the on-screen text at the end of an episode of my favorite series once read: "To Be Continued".
Maybe im stupid here but can someone explain ti me how were they able to read, digest, understand and made the decision about all this Pfizer documents within a year but are unable to just submit them to the public and needs 50 years to do?
Am i missing something here? Wouldn't be easier to release all documents than comprehend tham?