ANOTHER LICENSED FUNERAL DIRECTOR AND EMBALMER TELLS ABOUT FIBROUS WHITE BLOOD CLOTS

From the Canadian National Citizens Inquiry

Following on from my Substack of 21 January (CLICK HERE), an experienced licensed Funeral Director and embalmer has reconfirmed, at the Canadian National Citizens Inquiry, the presence of mysterious white fibrous blood clots extracted from bodies after the Covid “vaccine” rollout in 2021 along with pinhead size clotting. CLICK HERE to view (43 min). She had never seen this previously.

Embalmer Laura Jeffery testified that other embalmers reported to her seeing similar clotting especially in healthy middle aged individuals but they are reluctant to come forward. Unfortunately, she also reported that autopsies were discouraged so the cause of death in suspect cases was not documented.

Normally, a single anecdotal observation of this potential safety significance with a strong temporal relationship to the Covid injections would trigger an immediate drug regulator investigation. However, despite this testimony and similar credible reports, so far there has been no government investigation or apparent concern. The Excess Death rate in Australia is still unexplained and the government has refused to mount a formal inquiry into Excess Deaths.  

REVOLVING DOOR

Every problem is an opportunity……

Surprise…surprise.  Australia’s recently retired chief drug regulator joins the board of Medicines Australia – the peak lobby organisation which represents the interests of the pharmaceutical industry.

Apparently, Dr. Skerritt is committed to introducing many more mRNA products into Australia despite having been reported to be fraught with monumental issues of quality, safety and efficacy issues.  Presumably he is being well paid for his support.  The pharmaceutical industry must be delighted to have him “on board”.

A similar revolving door system exists in the US where many senior FDA officers have accepted very high paying jobs by “joining the other team” and potentially using their connections to facilitate new drug approvals.   The question is: Is this in the best interest of the public?  The answer seems obvious.

Readers should go to Dr. Maryanne Demasi’s Substack of 22 January for a more detailed account. CLICK HERE to view.

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