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So far so good in this regard. Momma tried, Momma tried--

First thing I remember knowin'

Was a lonesome whistle blowin'

And a youngun's dream of growin' up to ride

On a freight train leavin' town,

Not knowin' where I's bound

No one could change my mind but mama tried

One and only rebel child

In a family meek and mild,

Mama seemed to know what lay in store

In spite of all my Sunday learnin',

For the bad I kept on turnin'

Mama couldn't hold me anymore

And I turned twenty one in prison

Doin' life without parole

No one could steer me right

But mama tried, mama tried,

Mama tried to raise me better

But her pleadin' I denied,

That leaves only me to blame 'cause mama tried

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author

Going to hell in a bucket, but at least I'm enjoying the ride.

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Nov 22, 2022Liked by Stegiel

& a fun time will be had by all, eh...quelle horreur...

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I say if we are going to hell in a handbasket, at least make it our own handbasket.

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author

https://bailiwicknews.substack.com/p/stopping-conditions?utm_source=substack&utm_campaign=post_embed&utm_medium=web

NUTSHELL: US Government since 1969 has incrementally transferred/hidden the joint DOD+HHS Chemical and Biological Warfare Program (50 USC 32) in the Public Health Service Act (42 USC 201) and Food Drug and Cosmetics Act (21 USC 9), such that federally-funded, federally-directed public health programs and products are actually bioterrorism programs and biological and chemical weapon attacks.

The government's purpose is to commit mass murder/depopulate the world, without public knowledge and without legal consequence, and enslave survivors for wealth and power centralization through digitized 'vaccine' passports and digital currencies, without public knowledge and without public resistance.

21 USC 360bbb-3, Authorization for medical products for use in emergencies, is one of the key pseudo-laws enabling the bioweapon attacks under the Covid-19 national emergency pretext.

21 USC 360bbb-3(k) is one of the key provisions:

(k) If a product is the subject of an authorization under this section, the use of such product within the scope of the authorization shall not be considered to constitute a clinical investigation for purposes of section 355(i), 360b(j), or 360j(g) of this title or any other provision of this chapter or section 351 of the Public Health Service Act [42 U.S.C. 262].

There is widespread public perception that Covid-19 information campaigns, masks, diagnostic tests, treatments and injectables are components in a public health program using experimental but regulated, ‘safe and effective’ medical products for the purpose of saving lives during a public health emergency.

They are not.

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Quite a bit to digest. Thanks.

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Great pragmatic post Stegiel.

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