1,000,000 views on Twitter in 5 hours and Project Veritas doesn’t have an account. That’s the power of the #VeritasArmy and #DistributionByProxy

KEEP TWEETING: https://ctt.ec/qc994

"How many children were sacrificed to Satan for the vaccine?"

FINALLY THEY SPEAK IN PUBLIC ABOUT IT!
The Great awakening just startet!

"Wie viele Kinder wurden dem Satan für den Impfstoff geopfert?"

ENDLICH SPRECHEN SIE ÖFFENTLICH DARÜBER !
Das große Erwachen hat gerade begonnen!

🔥THIS IS MASSIVE !!! A Member of The FDA Vax Panel Today Said... "We Are Killing More People Than We Are Saving With The Shots" 
Please Share!!!
Subscribe and share my channel
👇👇
🆔@SergeantRobertHorton

@jamesokeefeiii Instagram livestream

https://www.instagram.com/tv/CUEWug7q_zN/?utm_medium=copy_link

JUST IN - France: “The American choice to exclude a European ally & partner such as France from a structuring partnership with Australia, at a time when we are facing unprecedented challenges in the Indo-Pacific … shows a lack of coherence that France can only note & regret.”

“The regrettable decision that has just been announced regarding the FSP program only reinforces the need to make the issue of European strategic autonomy loud and clear.”

Joint Statement by the Foreign Minister and Minister of Armed Forces of France.

@disclosetv

NEW - Facebook starts to censor "inconvenient climate change data": Temperature increases from 2000-2019 resulted in 116k heat deaths, but also 283k fewer cold deaths, according to a study published in the Lancet.

Facebook and its "fact-checkers" have scrambled: "Fake news".

https://twitter.com/BjornLomborg/status/1439963133683109895

@disclosetv

NEW - German government wants to censor the U.S. social media network Gab.com over "fake news".

https://news.gab.com/2021/09/20/germany-wants-to-force-gab-to-censor-its-not-happening/

@disclosetv

On Monday, an international group of vaccine experts, including officials from both the #FDA and the WHO, came out and said that there is no evidence suggesting that the general population needs to get COVID-19 vaccine #BoosterShots.

🔥Watch the full episode 👉https://youtu.be/ngpZAJksvSk

On Friday, the #FDA’s vaccine advisory panel met, debated, and ultimately voted against approving vaccine #BoosterShots for the general public.

However, according to statements from the White House, as well as other government officials, it sounds like they might not listen to this advisory panel, and roll out booster shots anyway.

🔥WATCH HERE👉https://youtu.be/0KH8G8ngT2U

We sat down with the former #ActingDirector of national intelligence under President Donald #Trump and discussed how the #ChineseCommunistParty is working to undermine America from within.

⭕️ Watch on @EpochTV 👉https://ept.ms/ChineseCommunistCrisis
⭕️ Get 10 videos FREE with just your email @EpochTV 👉 https://ept.ms/3j4SOkz

Yesterday, this is what a Tradie said to that Channel 7 Reporter who got hit with a Energy drink today.

(Scroll up if you want to see the energy drink situation)

@THEFIVE8TAKE -
AUSSIE STRONG 🇦🇺

Make sure we can send you Part 2 directly. Sign up now: CovidVaxExposed.com

Construction workers marching on Melbourne right now after building sites were ordered to close for 2 weeks, authorities are trying to break them into complying to be injected with the experimental covid vaccine, resist!

💥 Presidente Bolsonaro em um jantar luxuoso em Nova York - President Bolsonaro at a luxury dinner in New York
- Präsident Bolsonaro beim Luxusdinner in New York.

According to EU law, Comirnaty (Pfizer/Biontech) may from 22. December 2021 will no longer be vaccinated
The deadline for Moderna is the 6th. January 2021.
The deadline for AstraZeneca is the 29th. January 2021.
The deadline for Johnson&Johnson is the 11th. March 2021.
The background to this statement is the fact that - contrary to everything the political actors say - no vaccine against COVID-19 has received full approval from the European Medicines Agency (EMA). If you read what the EMA does to do e.g. Comirnaty, then you still read the following (the same information can be found about Vaxzevria or Spikevax) (pic in article) You can or must read this passage in such a way that Comirnaty has received a "CONDITIONAL DISTRIBUTION APPROVAL" because of his claimed effectiveness of 95%. Then effectiveness would be a prerequisite for this conditional authorization, for the conditional marketing authorization, which is being mentioned here. Such conditional market approval entails a number of inconveniences, which are probably the reason why political actors and their vassals are currently promoting vaccines such as market criers, in the hope of getting as much vaccine as possible in the upper arms until the deadlines we have mentioned above are reached in order to reduce the costs of vaccines that can no longer be.
[..] Now one could assume that the manufacturers of the COVID-19 vaccines speculate on obtaining full market approval from the EMA by the end of the year. However, this is only possible if the EMA completely breaks with all the rules it has given itself. Annex 1 to EU Regulation 2003/63/EC lists in detail the conditions that must be met in order to be able to apply for market approval at all, i.e. ordinary, non-conditional market approval. Even in the best case, at least 210 days pass between the application and decision of the CHMP, whereby the completion of phase III trials, which usually take at least two years, is one of the prerequisites for being able to submit an application for full admission at all. So if the EMA adheres to its own rules, there is no possibility that there will be a full market authorization for the COVID-19 vaccines before the conditional market authorization expires. This would mean vaccination from 22. December 2020 (Comirnaty), 6. January 2022 (Spikvax/Moderna) from 29. January 2022 (Vaxzevria/AstraZeneca), from 11. March (Johnson&Johnson) illegal.
This may explain the hustle and bustle that has gripped the vaccinees.
A request from us to the EMA is currently pending, as soon as we have received a response, we will continue this SAGA.

https://sciencefiles.org/2021/09/21/nach-eu-recht-darf-comirnaty-pfizer-biontech-ab-22-dezember-2021-nicht-mehr-verimpft-werden/

Nach EU-Recht darf Comirnaty (Pfizer/Biontech) ab 22. Dezember 2021 nicht mehr geimpft werden
Die Frist für Moderna ist der 6. Januar 2021.
Die Frist für AstraZeneca ist der 29. Januar 2021.
Die Frist für Johnson&Johnson ist der 11. März 2021.
Hintergrund dieser Aussage ist die Tatsache, dass - entgegen allem, was die politischen Akteure sagen - kein Impfstoff gegen COVID-19 von der Europäischen Arzneimittelbehörde (EMA) vollständig zugelassen wurde. Wenn man liest, was die EMA z.B. mit Comirnaty macht, dann liest man noch folgendes (die gleichen Informationen findet man auch über Vaxzevria oder Spikevax) (Bild im Artikel) Man kann oder muss diese Passage so lesen, dass Comirnaty wegen seiner behaupteten Wirksamkeit von 95% eine "CONDITIONAL DISTRIBUTION APPROVAL" erhalten hat. Dann wäre die Wirksamkeit eine Voraussetzung für diese bedingte Zulassung, für die bedingte Marktzulassung, von der hier die Rede ist. Eine solche bedingte Marktzulassung bringt eine Reihe von Unannehmlichkeiten mit sich, die wahrscheinlich der Grund dafür sind, dass politische Akteure und ihre Vasallen derzeit wie Marktschreier für Impfstoffe werben, in der Hoffnung, bis zum Erreichen der oben genannten Fristen möglichst viel Impfstoff in die Oberarme zu bekommen, um die Kosten für Impfstoffe, die nicht mehr sein können, zu senken.
[...] Nun könnte man annehmen, dass die Hersteller der COVID-19-Impfstoffe darauf spekulieren, bis Ende des Jahres die volle Marktzulassung von der EMA zu erhalten. Das ist aber nur möglich, wenn die EMA alle Regeln, die sie sich selbst gegeben hat, komplett bricht. Anhang 1 der EU-Verordnung 2003/63/EG listet detailliert die Bedingungen auf, die erfüllt sein müssen, um überhaupt eine Marktzulassung, also eine ordentliche, nicht an Bedingungen geknüpfte Marktzulassung, beantragen zu können. Selbst im günstigsten Fall vergehen zwischen Antrag und Entscheidung des CHMP mindestens 210 Tage, wobei der Abschluss von Phase III-Studien, die in der Regel mindestens zwei Jahre dauern, eine der Voraussetzungen ist, um überhaupt einen Antrag auf Vollzulassung stellen zu können. Hält sich die EMA also an ihre eigenen Regeln, besteht keine Möglichkeit, dass es vor Ablauf der bedingten Marktzulassung eine volle Marktzulassung für die COVID-19-Impfstoffe geben wird. Dies würde bedeuten, dass die Impfung ab 22. Dezember 2020 (Comirnaty), 6. Januar 2022 (Spikvax/Moderna) ab 29. Januar 2022 (Vaxzevria/AstraZeneca), ab 11. März (Johnson&Johnson) illegal.
Dies könnte eine Erklärung für die Hektik sein, die die Impflinge ergriffen hat.
Eine Anfrage von uns an die EMA steht derzeit noch aus; sobald wir eine Antwort erhalten haben, werden wir diese SAGA fortsetzen.

https://sciencefiles.org/2021/09/21/nach-eu-recht-darf-comirnaty-pfizer-biontech-ab-22-dezember-2021-nicht-mehr-verimpft-werden/

It’s well and truly on.

Aussies are fighting back.

And it’s great to see.

👊🏻🇬🇧🇦🇺