The information in this article was available to the Vaccine Advisory Committee before they made a decision. I pray that everyone reads this article and realizes the truth.
The government is wholly illegitimate!!!
Schizer has already admitted to fraud in court and his defense is that the US government was a co-conspirator.
Isn't that enough to shelve these toxins permanently?
My sources say most of the information and data was received so late in the game that no one in the FDA/CDC etc had enough time to go through all of it and make an informed decision. Even if they did get it in enough time they already know what they are going to do. Money comes before disposable human life. It is up to WE THE PEOPLE to refuse this shot under any and all circumstances.
Thank you! James Roguski and everyone exposing and opposing tyranny.
This Zoom call with Dr. David E. Martin and a group of Canadian scientists and activists was uploaded to Rumble May 17, 2022. It is a hard-hitting and concise summary of the legal tack he’s taking against COVID Genocide and the status of Dr. Martin’s lawsuits against the primary individuals responsible. https://forbiddenknowledgetv.net/dr-david-e-martin-gives-explosive-jaw-dropping-information-in-canadian-zoom-meeting/
Thank you for your excellent research and courage. God bless you Mr. Roguski. You are truly an advocate for children and parents.
This is an attempt at a holistic alternative - if anyone tries it, for even a short time, they will see. Although Uropathy is not a main point, it is mentioned as perhaps *the* most effective personal medicine on the planet. It is free, and can never be banned; however, there is no need as we have banned it ourselves!! Unfortunately, it also seems that, as well as Pharma, 'alternative' sites are not too keen on the subject. Do not want to lose supplement sales, I suppose: https://evolutionaryhealthplan.info/#_Ref40644295
Yes, all of us are praying. May God the righteous Judge now act.
“O my people, your guides mislead you and they have swallowed up the course of your paths. The Lord has taken his place to contend; he stands to judge peoples. The Lord will enter into judgment with the elders and princes of his people.” Isaiah 3:12-13
I will do exactly that prayer many times.
Thank you James.
I will also include my sisters to do the same.
James did you see this?
Fortune: WHO to convene emergency committee on monkeypox: ‘It’s now clear there is an unusual situation’
The meeting will take place on Thursday, June 23, WHO director general Dr. Tedros Adhanom Ghebreyesu announced at a Tuesday media event.
14/6/22: Monkeypox: WHO to convene emergency committee to assess virus' threat | FULL
WHO YT: Monkeypox starts @13:12; announcement @15:52 & @23:50 > 25:42 (after journalist question about it) (then on to Hepatitis) @27:05 short clarification on Monkeypox meeting: Thursday 23 June 2022; followed by Q&A discussion about the upcoming meeting and Monkeypox.
From GETTER: 澳喜农场多语组@MLGHA 22h
Japanese MPs tell the truth behind the pandemic:
Japanese MPs pointed out that what is happening now is an information warfare. And international capital manipulates technology giant companies to block the truth. The Japanese government works hand in glove with the the medical association to fabricate the covid-19 pandemic and create panic. They use administration power to make vaccines compulsory. The separation of powers in a democracy, the independence of the executive and the independence of the judiciary, have completely failed, and the law only served the authoritarian power. In order to avoid more victims, people should stand up and fight, and believe that through everyone’s efforts, the current dark situation can be changed.
Please see the excellent interview James Roguski did with Vaccine Choice Canada.
Recent VCC Guests
Oppose the Fraud - James Roguski - June 9
Details on: OpposetheFraud.com
Video Link: https://librti.com/page/view-video?id=2954
It’s beyond deplorable tyrannical seditious practices! Can’t even believe this is nodded in USA...it’s Euthanasia Utilization Authoritarianism (EUA) that’s the truth! Georgia Guidestones tell it they seek it be no more than 500,000,000 and that’d be themselves alone all on the globe!
Thanks, James, for all the hours and brainwork you put into this. May God Bless, Protect you and give you Strength !
URGENT! JAMES! ACIP meeting Fri/Sat 17/18 June
BREAKING NEWS: CDC launches sneak attack; the ACIP will meet TOMORROW (Friday, June 17) and Saturday, June 18 to extend the mRNA Final Solution to little kids
The White House has kept these meetings a secret until now
https://www.cdc.gov/vaccines/acip/meetings/ (public comments tab)
Found this via: https://tobyrogers.substack.com/p/breaking-news-cdc-launches-sneak
When will a vaccine be available for children under 5?
The FDA will decide the vaccine authorization details for children under 5 on June 15. Then, the Centers for Disease Control and Prevention’s (CDC) Advisory Committee on Immunization Practices (ACIP) will meet June 17 and 18 to review the FDA’s information and possibly make a recommendation on the use of Pfizer and Moderna vaccines for young children, and on use of the Moderna vaccine for children 6 and up. Following the ACIP meeting, the Western States Scientific Safety Review Workgroup will meet to say whether they agree with the recommendation. If they do, the vaccine will then be available in Washington state for the new age groups.
Food & Drug Administration - 17/6/22 - 3.30pm UK
Virtual Press Conference: Pediatric COVID-19 Vaccines
Join us for a virtual press conference to discuss the FDA’s emergency use authorization of the Moderna COVID-19 Vaccine and the Pfizer-BioNTech COVID-19 Vaccine for the prevention of COVID-19 to include use in children down to six months of age. FDA Commissioner Dr. Robert M. Califf and FDA's Center for Biologics Evaluation and Research Director Dr. Peter Marks will be taking questions.
COVID-19 injectable bioweapons as case study in legalized, government-operated domestic bioterrorism.
Use of EUA-covered medical countermeasure (MCM) products including masks, PCR tests, mRNA and DNA injections, and other drugs, devices and biologics, once designated as such by the Secretary of Health and Human Services (March 10, 2020, retroactive to February 4, 2020) “shall not be considered to constitute a clinical investigation.” 21 USC 360bbb-3(k) as adopted 1997 and amended 2004, 2005, 2013.
This is true no matter how untested, unmonitored, unsafe, or ineffective they are, no matter whether their harmfulness to human health and uselessness for infection-control are known before use, or discovered afterward.
Legal implications derived from the main premise:
-There is no stopping condition.
-EUA products are exempt from laws regulating researcher use of investigational, experimental drugs, devices and biologics on human beings.
-EUA products are exempt from laws regulating physician use of approved drugs, devices and biologics as medical treatments for patients.
-There are no manufacturers of experimental products (EUA products are not part of any clinical investigation, and therefore not experimental.)
-There are no government or private contracts for purchase of experimental products; there are only contracts for ‘large scale vaccine manufacturing demonstrations.’
-There is no act of administration of any experimental products.
-There are no nurses or pharmacists administering experimental products.
-There are no human subjects (of experiments) or patients (of physicians providing treatment) receiving experimental products: no victims.
-There is no party responsible for the wellbeing of recipients after administration of EUA products.
-There is no treatment group and no control group.
-Human beings administering EUA products have no informed consent obligations to provide information about ingredients, risks, benefits, alternatives, or the option to accept or refuse the products. See 21 USC 360bbb-3(e)(1)(A)(ii)) waiving informed consent for unapproved products (2004); 21 USC 360bbb-3(e)(2)(A) waiving informed consent for unapproved use of an approved product (2004); 21 USC 355(i)(4) waiving informed consent for experimental products classified by HHS as ‘minimal risk’ drugs (2016); 21 USC 360j(g)(3) waiving informed consent for experimental ‘minimal risk’ devices (2016).
-Human beings receiving EUA products have no informed consent rights to receive information about ingredients, risks, benefits, alternatives, or the option to accept or refuse the products. See citations, bullet point above.
-There are no Institutional Review Boards supervising administration of the experimental products.
-There are no safety standards for EUA products.
-There are no efficacy standard for EUA products. See 21 USC 360bbb-3(c)(2)(A), 1997, 2004, re: ‘may be effective’