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CALLING ALL HEALTH PROFESSIONALS

Prosecutions are ramping up. Thank you one and all for continuing to stand in your truth.

We work with so many humble souls, quietly achieving some incredible things. I personally am in awe of the energy we all continue to have to create a better way.

There is a team working on criminal prosecutions (not class actions) in Queensland, Australia.

Leanne Bartrim is an ex QLD Health retired forensic investigator.  She's working with retired detectives and lawyers in relation to criminal proceedings against the government.

Leanne is requesting members of public/healthcare workers to reach out re vax injuries, whistle-blowers etc. Also wanting people who have suffered vaccine injuries or lost jobs or have letters from governing bodies such as AHPRA, schools etc. The email she is using for this is lucyb4457@gmail.com

Please contact her or pass this on to anyone you feel is ready to share their experience. 🙏

Blessings
🕊💫🕊
Forwarded from Tommy Robinson News
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Q and A on Australian TV about the Russia/Ukraine situation

Young man of Russian heritage is heckled by everyone while asking his question, then ejected from the show by the host!
Forwarded from WA Conscious Businesses
ATTENTION - THURSDAY WEEKLY
EMPLOYEE FOCUSED ZOOM SEMINAR
WITH PAUL RICHARDSON

THIS THURSDAY NIGHT - ZOOM PRESENTATION TO EMPLOYEES WITH PAUL RICHARDSON 6PM (WST - Perth)

https://us02web.zoom.us/j/89868968712
Steve Kirsch:

'Pfizer claimed repeatedly in their documents to the FDA that their vaccine would “prevent” COVID-19.

Pfizer knew the injection’s adverse effects would increase with more injections of continuing boosters.

Pfizer knew their injections did not stay at the injection site.

Pfizer knew that the vaccinated group reported far more systemic adverse events than the placebo group.

Pfizer knew that the efficacy of the vaccine waned very quickly over time; by as much as 50% in as little as 1 month after the second dose. How come we weren’t warned about that???

Pfizer defended VAERS (because they didn’t want extra reporting cost burdens).

There are six individuals that signed up for two different clinical trials at two different sites which is really odd.

Pfizer knew vaccinated individuals could still catch COVID-19 and test positive.

There are 1,448 pages comprising 9,704 individual subjects who were excluded from the trials. There isn’t enough detail to know why.

Pfizer paid $2,875,842.00 for their application to the FDA. This is more of a point of information for now.

It is troubling that Pfizer redacts information that is not proprietary that would be very helpful in assessing the data such as the number of doses administered in the ADVERSE EVENTS OF SPECIAL INTEREST” (AESI) document (aka the 5.3.6 document).

Pfizer only tests you for COVID if you have at least one symptom. If the vaccine suppresses symptoms (which it apparently does), then it will falsely appear as if the vaccine reduces the number of COVID cases.

How could anaphylaxis not show up in the Phase 3 trial on any of the 44,000 patients, yet show up as a major safety concern in the post-marketing document?!?'

https://stevekirsch.substack.com/p/10-things-you-should-know-about-the?s=r
Pfizer report from Jan 2021 for the Australian Government shows they had concerns over long-term immunity

"Antibodies and T cells in monkeys declined quickly over 5 weeks after the second dose"

Report: https://www.tga.gov.au/sites/default/files/foi-2389-06.pdf
This is what Stephane Bancel, the founding CEO of Moderna, said about mRNA technology back in 2016.

“Delivery — actually getting RNA into cells — has long bedeviled the whole field. On their own, RNA molecules have a hard time reaching their targets. They work better if they’re wrapped up in a delivery mechanism, such as nanoparticles made of lipids. But those nanoparticles can lead to dangerous side effects, especially if a patient has to take repeated doses over months or years.
Novartis abandoned the related realm of RNA interference over concerns about toxicity, as did Merck and Roche…”

And, from the Vice President of BioNTech.

“I would say that mRNA is better suited for diseases where treatment for short duration is sufficiently curative, so the toxicities caused by delivery materials are less likely to occur,” said Katalin Karikó, a pioneer in the field who serves as a vice president at BioNTech.
Forwarded from Zeee Media 🎙
This is good news, but will anything eventuate from it?

@zeeemedia
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