SCAMS-R-US

[XenaLives]

Food for thought:

"They" control the media... but to a great extent they have also controlled the publishing of books throughout history. I took honors U.S. History in the late '60s. I had a dedicated, passionate teacher but she could only teach what was in the books.

I never heard about Prescott Bush and the plot to overthrow FDR because it wasn't allowed in the textbook and the curriculum. His son and grandson would not have been elect president if the books had not been censored.

The plot:

https://www.arcadiapublishing.com/Navigation/Community/Arcadia-and-THP-Blog/September-2018/Smedley-Butler-and-the-1930s-Plot-to-Overthrow-the

The man that stopped it:
https://taskandpurpose.com/opinion/smedley-butler-gangsters-of-capitalism/

The Congressional Hearings he participated in:
https://en.wikisource.org/wiki/McCormack%E2%80%93Dickstein_Committee

[XenaLives]

Your video at this time - important...

https://youtu.be/rcDoAOCEMLw?t=1341

[XenaLives]

Your video makes the point that the Federal Reserve is the largest landlord in the country. So if WE THE PEOPLE are able to restore democracy we can tie rents to a living wage.

Praying for a Spiritual and intellectual reawakening in this country.

[XenaLives]

"Conspiracy theorists" are realists in this world.

[chickenvestor]

This guy seems to put the storm that is coming in a clear format. We need to get ready for what is going to happen over the next few months.

[XenaLives]

Ivermectin could have saved thousands of lives in the "pandemic"...

The scientific process was corrupted. Punch line is 35 minutes in, but good info is before this.


https://cms.megaphone.fm/channel/BMDC8713803568?selected=BMDC8408726302

[XenaLives]

At some point medical practice needs to stop treating symptoms and start treating the cause of the disease. Long term conditions and diseases of aging are usually due to systemic dysfunction on the mitochondrial level. Treating symptoms just leads to additional dysfunction known as "side effects".

These commercials drive me crazy. Physicians frequently over prescribe and improperly prescribe psychiatric meds, see this link:t.ly/dRGi

https://www.youtube.com/watch?v=5JAE28ts_3M

https://www.youtube.com/watch?v=gLB5XWAQzBE

[XenaLives]

An excellent presentation on the primary failure in the U.S. healthcare system.

https://www.youtube.com/watch?v=arrokG3wCdE

[XenaLives]

There is scientific evidence that both the COVID vaccine and the disease cause serious cardiac and vascular changes. Blarcamesine may alleviate some of these effects, it is unknown; but it can not be denied that it is medical history that must be taken into account when evaluating patient response.


You can follow the author on twitter:
https://twitter.com/FlavioCadegiani



https://www.researchgate.net/publication/358834540_Catecholamines_are_the_key_trigger_of_mRNA_SARS-CoV-2_and_mRNA_COVID-19_vaccine-induced_myocarditis_and_sudden_deaths_a_compelling_hypothesis_supported_by_epidemiological_anatomopathological_molecular

[XenaLives]

This is hysterical!!!
Note the woman in the background who's cracking up too...

https://rumble.com/vvie58-dutch-mp-gideon-van-meijeren-confronts-globalist-pm-rutte-for-his-world-eco.html

[XenaLives]

Paper on patented Moderna gene sequence found in SARS...

https://archive.is/2021.12.28-100420/https://arkmedic.substack.com/p/how-to-blast-your-way-to-the-truth#selection-685.72-685.85

[XenaLives]

Issues with the COVID vaccine:

https://www.youtube.com/watch?v=6nSXHrmOy8o

[chickenvestor]

Got to get past the music at the start of this. This hedge fund manager sees a very bad outcome for the big pharma vax pushers when the narrative can no longer stand.

https://paine.tv/listen-are-moderna-and-pfizer-the-next-enrons-former-blackrock-hedge-fund-guru-edward-dowd-paints-grim-picture-for-big-pharmas-vax-kings-while-big-insurance-appears-prepped-to-go-to-war-with/

[XenaLives]

Before you watch this I want point out two things:

1) Prescott Bush and others tried to organize a military coup to overthrow the first guy. https://bit.ly/3o6J50J

1) There is no clip of JFK promoting this political construct:

The New World Order is just a crazy conspiracy theory that definitely isn't real and this video proves it!pic.twitter.com/BIbHxjdcGr

— Critical Thinking 101(Expert of Expert Evaluation) (@critica18495985) January 19, 2022

[XenaLives]

Vera --- more on genocide...

https://www.youtube.com/watch?v=CU4GKFLiR_c

[XenaLives]

Holocaust survivor explains the danger of COVID fear mongering.

https://youtu.be/PdlWhuUFuKs

[XenaLives]

Doctors explain how Pharma for profit is killing people:

https://thehighwire.com/watch/

[XenaLives]

From a physcian to the FDA 12/8/2020, excerpt:

I am a pediatric specialist caring for children with the multisystem inflammatory syndrome (MIS-C). I am concerned about the possibility that the new vaccines aimed at creating immunity against the SARS-CoV-2 spike protein (including the mRNA vaccines of Moderna and Pfizer) have the potential to cause microvascular injury to the brain, heart, liver, and kidneys in a way that does not currently appear to be assessed in safety trials of these potential drugs.

Puntmann et al. (JAMA Cardiol. 2020;5:1265-1273) showed that the prospective study of 100 German patients who were recently recovered from COVID-19 revealed significant cardiac involvement on cardiac MRI scans in 78% of them, an average 2-1/2 months after their recovery from the acute illness. Two-thirds of these patients were never hospitalized, and there was ongoing myocardial inflammation in 60%. The abnormalities occurred independent of preexisting conditions, severity of the initial disease, and overall course of the acute illness.

Full text here:
https://www.regulations.gov/document/FDA-2020-N-1898-0246

[XenaLives]

This study was funded by the Bill and Melinda Gates Foundation:

Clinical trial conducted by MedinCell confirms the safety of continuous administration of ivermectin

Euronext: MEDCL • Montpellier - France • April 19, 2021 - 5:45pm CEST
Clinical trial validates the safety of ivermectin taken daily in oral form, to simulate the continuous release of the active substance by a long-acting injection. No side effects were observed with the three doses of ivermectin tested up to 100 µg / kg.

MedinCell develops several long-acting injectable formulations of ivermectin, the most advanced aims at preventing infection from Covid-19 and its mutants for several months.

Positive results of the safety study
"All our programs are developed in accordance with the highest ethical standards and on the basis of reliable scientific principles with a view to potential massive deployment. Proving the safety of ivermectin in regular daily administration over a long period was an essential step for our ivermectin programs, in particular mdc-TTG in Covid-19," said Joël Richard, Chief Development Officer at
MedinCell.

Ivermectin has already been administered as a once-daily treatment to hundreds of millions of patients worldwide. Its safety as a once-daily treatment has been demonstrated and documented. MedinCell tested ivermectin taken daily in oral form to simulate the continuous release of the active substance by a long-acting injectable. After completion,the study confirms the safety of ivermectin up to a dose of 100 µg / kg / day in continuous administration over 1 month in healthy volunteers. No significant difference was observed between the treated volunteers and the placebo volunteers in the three cohorts studied successively (daily doses of 50 µg / kg, 75 µg / kg and 100 µg / kg respectively).

The pharmacokinetic data of the three cohorts shows a limited peak circulating plasma concentration in the first 12 hours (Cmax between 25-60 ng / mL) and the rapid achievement of a stationary regime and a regular plasma concentration of between approximately 10 and 30 ng / mL for 28 days, depending on the dose administered. These preliminary results are considered positive and live up to Company expectations based on the data in the literature. The dose-response relationship has not yet been established.

After study completion and in regard of the expert review conducted by Professor Jacques Descotes1 (March 2021), the
safety profile of ivermectin supports the progress of MedinCell programs using this molecule, in particular mdc-TTG
against Covid-19 and mdc-STM against malaria.

https://www.medincell.com/wp-content/uploads/2021/04/CP-IVM-Phase1-avril2021_EN_vf-ok.pdf

[XenaLives]

Fauci apparently lied to Congress:

https://www.youtube.com/watch?v=_zgoENmeddA

[eom7]

Replied on ADN board... not sure what I posted that here. Sorry

[XenaLives]

Great Britain: Excess Mortality Among Children After Vaccine Rollout

Is it just a coincidence that deaths among children have increased by 62% since the rollout of the mRNA shots (up to 400% in vulnerable children) against the five-year average?

Deaths of children have been on the rise since the UK started vaccinating teenagers from the age of 12 and older. The risk-benefit analysis raises serious doubts about injecting this age group with the experimental drug.

On September 20, the British national health service NHS announced that the coronavirus vaccine would be rolled out for children aged 12 to 15. In part of the biggest vaccination drive in the country’s health service history, nearly three million children can receive a first dose of the Pfizer vaccine. According to the NHS, jabs started in hundreds of schools (week 38), with the injection program rolling out to others in the coming weeks.


more...

https://rairfoundation.com/great-britain-excess-mortality-among-children-after-vaccine-rollout/

[XenaLives]

For those who think wearing a mask makes sense:

https://www.covidtruths.co.uk/wp-content/uploads/2020/07/VARIOUS-FACE-MASK-STUDIES-PROVE-THEIR-INEFFECTIVENESS-PDF.pdf

[XenaLives]

Did you see this?

https://investorshub.advfn.com/boards/read_msg.aspx?message_id=166957538

[XenaLives]

You can't convince me that COVID wasn't planned and seeded.

I am on "the list". My significant other from the '70s was affiliated with "military intelligence". He died in 2019, and in late 2019 I had four trips to the ER with no diagnosis..

I suspect it was early COVID. There are others , some highly placed who believe that at about the same time as this meeting COVID was seeded in the U.S. popluation.

https://www.youtube.com/watch?v=AoLw-Q8X174

[eom7]

When will we here from EU on hydrogen project?

[XenaLives]

Odd EOD trading pattern.. two trades right after the bell...

CEVA:

 
 11/30/21	16:00:17	44.10	44.10	44.55	700 
 11/30/21	16:00:01	44.10	43.93	44.55	41,600 
 11/30/21	16:00:01	44.13	44.08	44.55	41,671 
 11/30/21	15:59:46	44.16	44.11	44.20	585 
 11/30/21	15:59:46	44.15	44.10	44.15	500 
 11/30/21	15:54:40	44.135	43.93	44.08	1,097 
 11/30/21	15:49:44	44.44	44.38	44.46	675 
 11/30/21	15:39:55	44.25	44.26	44.43	800 
 

AVXL:

 
 1/30/21	16:00:02	19.40	19.29	19.44	782,000 
 11/30/21	16:00:01	19.365	19.29	19.44	780,508 
 11/30/21	15:59:57	19.365	19.36	19.37	700 
 11/30/21	15:59:56	19.3601	19.36	19.37	1,102 
 11/30/21	15:59:54	19.37	19.36	19.37	1,200 
 11/30/21	15:59:54	19.365	19.36	19.37	2,805 
 11/30/21	15:59:49	19.37	19.36	19.37	800 
 

LWLG:

 
 11/30/21	16:00:26	13.93	13.60	15.40	700 
 11/30/21	16:00:01	13.93	13.87	14.02	11,800 
 11/30/21	16:00:01	13.89	13.87	14.02	11,213 
 11/30/21	15:59:51	13.935	13.91	13.95	1,094 
 11/30/21	15:59:27	13.935	13.91	13.94	600 
 11/30/21	15:58:46	13.952	13.90	13.97	1,000 
 11/30/21	15:58:21	13.91	13.89	13.91	3,100 
 11/30/21	15:58:21	13.907	13.89	13.91	900 
 

ADN:

 
 11/30/21	16:00:20	7.66	7.60	9.50	1,900 
 11/30/21	16:00:02	7.66	7.60	7.69	65,400 
 11/30/21	16:00:01	7.64	7.60	7.69	65,320 
 11/30/21	15:59:50	7.65	7.65	7.68	576 
 11/30/21	15:59:35	7.65	7.64	7.65	500 
 11/30/21	15:59:21	7.65	7.64	7.65	700 
 11/30/21	15:59:15	7.65	7.64	7.65	500 
 11/30/21	15:59:04	7.645	7.64	7.65	800 
 

FCEL:

 
 11/30/21	16:00:14	8.68	8.65	8.70	1,500 
 11/30/21	16:00:13	8.68	8.65	8.70	3,600 
 11/30/21	16:00:01	8.68	8.65	8.70	421,400 
 11/30/21	16:00:01	8.69	8.65	8.70	421,411 
 11/30/21	16:00:00	8.70	8.68	8.69	5,366 
 11/30/21	15:59:59	8.70	8.68	8.69	900 
 11/30/21	15:59:59	8.69	8.68	8.69	500 
 11/30/21	15:59:59	8.69	8.68	8.69	30,443 
 11/30/21	15:59:56	8.69	8.69	8.70	1,500 
 

GFS:

 
 11/30/21	16:08:54	71.00	70.40	71.00	500 
 11/30/21	16:07:18	70.40	69.25	70.40	500 
 11/30/21	16:00:01	69.24	69.00	69.56	41,600 
 11/30/21	16:00:01	69.42	69.00	69.56	41,447 
 11/30/21	15:59:58	69.39	69.20	69.43	525 
 11/30/21	15:59:50	69.38	69.29	69.39	514 
 11/30/21	15:59:49	69.37	69.29	69.38	1,000 
 11/30/21	15:59:49	69.3799	69.29	69.38	3,300 
 11/30/21	15:59:48	69.37	69.29	69.38	1,000 
 

BB:

 
 11/30/21	16:17:35	9.5134	9.52	9.55	800 
 11/30/21	16:12:41	9.52	9.52	9.55	900 
 11/30/21	16:12:41	9.53	9.52	9.55	600 
 11/30/21	16:10:00	9.52	9.52	9.60	138,800 
 11/30/21	16:06:04	9.53	9.52	9.60	600 
 11/30/21	16:00:27	9.52	9.50	9.56	16,600 
 11/30/21	16:00:27	9.52	9.50	9.56	11,600 
 11/30/21	16:00:02	9.52	9.50	9.56	138,800 
 11/30/21	16:00:02	9.52	9.50	9.56	138,800 
 11/30/21	16:00:02	9.515	9.50	9.56	129,201 
 11/30/21	15:59:57	9.52	9.52	9.53	500 
 11/30/21	15:59:55	9.52	9.51	9.52	800 
 11/30/21	15:59:53	9.51	9.51	9.52	4,200 
 11/30/21	15:59:52	9.51	9.51	9.52	700 
 11/30/21	15:59:50	9.51	9.51	9.52	500 
 

IMGN:

 
 11/30/21	16:24:59	6.40	6.30	6.40	9,600 
 11/30/21	16:13:00	6.40	6.30	6.40	14,100 
 11/30/21	16:10:00	6.40	6.30	6.40	925,000 
 11/30/21	16:09:32	6.40	6.30	6.40	56,600 
 11/30/21	16:03:12	6.40	6.30	6.40	69,500 
 11/30/21	16:00:02	6.40	6.20	6.44	925,000 
 11/30/21	16:00:02	6.40	6.20	6.44	925,000 
 11/30/21	16:00:01	6.40	6.20	6.44	600 
 11/30/21	15:59:58	6.40	6.36	6.40	600 
 11/30/21	15:59:57	6.40	6.36	6.40	1,100 
 

RKLY:

 
 11/30/21	16:24:59	6.40	6.30	6.40	9,600 
 11/30/21	16:13:00	6.40	6.30	6.40	14,100 
 11/30/21	16:10:00	6.40	6.30	6.40	925,000 
 11/30/21	16:09:32	6.40	6.30	6.40	56,600 
 11/30/21	16:03:12	6.40	6.30	6.40	69,500 
 11/30/21	16:00:02	6.40	6.20	6.44	925,000 
 11/30/21	16:00:02	6.40	6.20	6.44	925,000 
 11/30/21	16:00:01	6.40	6.20	6.44	600 
 11/30/21	15:59:58	6.40	6.36	6.40	600 
 11/30/21	15:59:57	6.40	6.36	6.40	1,100 
 

FSR:

 
 11/30/21	16:14:26	21.39	21.41	21.60	2,900 
 11/30/21	16:10:00	21.39	21.38	21.60	197,400 
 11/30/21	16:01:51	21.39	21.35	21.60	1,500 
 11/30/21	16:00:52	21.39	21.35	21.60	1,800 
 11/30/21	16:00:52	21.3904	21.35	21.60	8,400 
 11/30/21	16:00:50	21.3874	21.35	21.60	4,800 
 11/30/21	16:00:43	21.39	21.35	21.60	2,700 
 11/30/21	16:00:43	21.39	21.35	21.60	1,800 
 11/30/21	16:00:20	21.39	21.35	21.60	1,900 
 11/30/21	16:00:20	21.39	21.35	21.60	2,100 
 11/30/21	16:00:19	21.39	21.35	21.60	1,000 
 11/30/21	16:00:19	21.39	21.35	21.60	600 
 11/30/21	16:00:02	21.39	21.35	21.62	197,400 
 11/30/21	16:00:02	21.39	21.35	21.62	197,400 
 11/30/21	15:59:59	21.41	21.39	21.41	927 
 11/30/21	15:59:58	21.41	21.39	21.40	593 
 11/30/21	15:59:52	21.405	21.39	21.40	700 
 11/30/21	15:59:52	21.40	21.39	21.40	2,223 
 

LIDR:

 
 11/30/21	16:12:57	5.5699	5.55	5.57	1,000 
 11/30/21	16:09:10	5.57	5.57	5.60	39,900 
 11/30/21	16:08:09	5.57	5.57	5.60	600 
 11/30/21	16:03:56	5.5699	5.55	5.57	239,000 
 11/30/21	16:03:44	5.5674	5.55	5.60	31,000 
 11/30/21	16:00:14	5.57	5.29	5.56	2,400 
 11/30/21	16:00:13	5.57	5.29	5.56	16,200 
 11/30/21	16:00:01	5.57	5.38	5.56	1,082,600 
 11/30/21	16:00:01	5.54	5.49	5.56	1,082,670 
 11/30/21	15:59:56	5.55	5.53	5.54	1,000 
 11/30/21	15:59:52	5.55	5.53	5.55	847 
 11/30/21	15:59:45	5.54	5.53	5.55	1,700 
 11/30/21	15:59:45	5.54	5.53	5.55	7,100 
 

VLDR:

 
 11/30/21	16:38:12	5.56	5.38	5.56	900 
 11/30/21	16:37:39	5.52	5.38	5.52	1,100 
 11/30/21	16:37:22	5.47	5.38	5.47	67,400 
 11/30/21	16:23:07	5.47	5.32	5.47	500 
 11/30/21	16:09:35	5.52	5.30	5.48	2,700 
 11/30/21	16:05:35	5.52	5.30	5.48	225,300 
 11/30/21	16:02:56	5.52	5.30	5.44	1,600 
 11/30/21	16:02:09	5.52	5.30	5.46	800 
 11/30/21	16:00:01	5.52	5.39	5.52	1,847,000 
 11/30/21	16:00:01	5.52	5.39	5.52	800 
 11/30/21	16:00:01	5.52	5.39	5.52	500 
 11/30/21	16:00:01	5.52	5.39	5.52	1,200 
 11/30/21	16:00:01	5.52	5.39	5.52	800 
 11/30/21	16:00:01	5.51	5.39	5.52	1,847,023 
 11/30/21	15:59:59	5.52	5.50	5.52	3,300 
 11/30/21	15:59:59	5.515	5.50	5.52	3,348 
 11/30/21	15:59:59	5.53	5.50	5.52	5,411 
 11/30/21	15:59:57	5.53	5.51	5.52	1,300 
 

AKBA:

 
 11/30/21	16:44:47	2.71	2.63	2.73	5,400 
 11/30/21	16:05:13	2.7099	2.63	2.73	28,500 
 11/30/21	16:05:09	2.7126	2.63	2.73	700 
 11/30/21	16:04:55	2.7074	2.63	2.73	14,000 
 11/30/21	16:03:04	2.71	2.63	2.73	1,900 
 11/30/21	16:00:14	2.71	2.62	2.73	3,300 
 11/30/21	16:00:13	2.71	2.62	2.73	2,200 
 11/30/21	16:00:01	2.71	2.69	2.73	488,400 
 11/30/21	16:00:01	2.70	2.69	2.72	488,172 
 11/30/21	15:59:59	2.71	2.70	2.71	1,060 
 11/30/21	15:59:59	2.705	2.70	2.71	828 
 

RIDE:

 
 11/30/21	16:41:26	4.68	4.60	4.64	3,000 
 11/30/21	16:40:28	4.64	4.64	4.68	5,000 
 11/30/21	16:30:16	4.6795	4.60	4.68	317,500 
 11/30/21	16:30:13	4.6795	4.60	4.68	128,800 
 11/30/21	16:24:36	4.62	4.61	4.68	500 
 11/30/21	16:24:11	4.68	4.61	4.68	1,000 
 11/30/21	16:24:11	4.68	4.61	4.68	1,000 
 11/30/21	16:09:20	4.67	4.61	4.68	1,700 
 11/30/21	16:03:18	4.6774	4.55	4.70	800 
 11/30/21	16:02:42	4.68	4.55	4.70	1,900 
 11/30/21	16:00:57	4.68	4.55	4.70	1,000 
 11/30/21	16:00:42	4.68	4.55	4.70	2,200 
 11/30/21	16:00:06	4.68	4.58	4.70	1,400 
 11/30/21	16:00:06	4.68	4.58	4.70	4,700 
 11/30/21	16:00:01	4.68	4.58	4.70	592,000 
 11/30/21	16:00:01	4.68	4.58	4.70	600 
 11/30/21	16:00:01	4.68	4.58	4.70	700 
 11/30/21	16:00:00	4.67	4.58	4.69	583,618 
 11/30/21	15:59:56	4.68	4.66	4.67	600 
 11/30/21	15:59:56	4.68	4.66	4.67	800 
 11/30/21	15:59:56	4.67	4.66	4.67	500 
 

DNA:

 
 11/30/21	16:36:46	11.86	11.84	11.86	500 
 11/30/21	16:10:00	11.87	11.55	12.05	1,294,900 
 11/30/21	16:07:03	11.87	11.92	12.05	2,800 
 11/30/21	16:00:45	11.87	11.75	12.05	700 
 11/30/21	16:00:02	11.87	11.75	11.92	1,294,900 
 11/30/21	16:00:02	11.87	11.75	11.92	1,294,900 
 11/30/21	16:00:01	11.86	11.75	11.92	1,500 
 11/30/21	16:00:00	11.86	11.81	11.92	1,500 
 11/30/21	16:00:00	11.86	11.81	11.92	500 
 11/30/21	16:00:00	11.86	11.81	11.92	1,400 
 
 
  
  
 OPTT: 
 
 
 11/30/21	16:16:33	2.00	1.96	2.00	500 
 11/30/21	16:16:33	1.9999	1.96	2.00	500 
 11/30/21	16:15:24	1.9699	1.96	1.97	2,000 
 11/30/21	16:10:00	2.02	1.96	2.00	272,700 
 11/30/21	16:09:24	1.96	1.96	1.97	800 
 11/30/21	16:05:10	1.97	1.97	2.01	9,100 
 11/30/21	16:05:10	1.97	1.97	2.01	5,700 
 11/30/21	16:05:10	1.98	1.97	2.01	5,100 
 11/30/21	16:03:30	2.00	1.95	2.00	3,100 
 11/30/21	16:03:30	2.00	1.95	2.00	1,000 
 11/30/21	16:00:34	1.96	1.95	2.03	1,600 
 11/30/21	16:00:01	2.02	2.00	2.03	272,700 
 11/30/21	16:00:01	2.02	2.00	2.03	272,700 
 11/30/21	16:00:01	2.02	2.00	2.03	272,700 
 11/30/21	16:00:00	2.0162	2.00	2.02	265,263 
 11/30/21	15:59:58	2.02	2.01	2.02	1,300 
 11/30/21	15:59:56	2.01	2.01	2.02	1,600 
 
 
  
 ATOS: 
 
 
 11/30/21	16:40:48	2.27	2.23	2.30	500 
 11/30/21	16:01:11	2.27	2.18	2.25	2,300 
 11/30/21	16:01:07	2.27	2.18	2.25	1,300 
 11/30/21	16:00:05	2.27	2.25	2.30	1,400 
 11/30/21	16:00:01	2.27	2.25	2.30	108,300 
 11/30/21	16:00:00	2.29	2.25	2.29	108,346 
 11/30/21	15:59:59	2.29	2.28	2.29	1,177 
 11/30/21	15:59:54	2.2821	2.28	2.29	500 
 11/30/21	15:59:53	2.285	2.28	2.29	600 
 
 
  
  
 cvM: 
 
  
 11/30/21	16:44:46	10.27	9.70	10.23	1,200 
 11/30/21	16:41:00	10.27	9.70	10.23	3,400 
 11/30/21	16:10:00	10.27	10.20	10.24	272,400 
 11/30/21	16:07:05	10.28	10.28	10.30	600 
 11/30/21	16:02:50	10.2674	10.20	10.32	700 
 11/30/21	16:00:01	10.27	10.24	10.32	1,800 
 11/30/21	16:00:01	10.27	10.24	10.32	900 
 11/30/21	16:00:01	10.27	10.24	10.30	272,400 
 11/30/21	16:00:01	10.27	10.24	10.30	272,400 
 11/30/21	16:00:01	10.27	10.24	10.30	272,400 
 11/30/21	16:00:00	10.24	10.24	10.30	275,513 
 11/30/21	15:59:21	10.21	10.24	10.27	800 
 11/30/21	15:59:21	10.24	10.24	10.27	2,183 
 11/30/21	15:59:19	10.23	10.21	10.24	561 
 11/30/21	15:59:07	10.21	10.21	10.24	599 
 11/30/21	15:58:45	10.20	10.20	10.25	2,000 
 
 
  
  
 VSTM: 
 
 
 11/30/21	16:01:45	2.67	2.64	2.68	1,900 
 11/30/21	16:01:36	2.64	2.64	2.68	700 
 11/30/21	16:00:36	2.67	2.64	2.67	3,400 
 11/30/21	16:00:09	2.67	2.64	2.67	500 
 11/30/21	16:00:09	2.67	2.64	2.67	1,800 
 11/30/21	16:00:01	2.67	2.65	2.68	1,015,400 
 11/30/21	16:00:01	2.66	2.65	2.68	1,015,558 
 11/30/21	16:00:00	2.66	2.66	2.67	737 
 11/30/21	15:59:55	2.67	2.66	2.67	600 
 11/30/21	15:59:55	2.67	2.66	2.67	1,000 
 11/30/21	15:59:55	2.67	2.66	2.67	2,236 
 
 
  
  
 CLVS: 
 
 
 11/30/21	16:03:03	3.16	3.16	3.17	1,200 
 11/30/21	16:02:15	3.1599	3.16	3.17	29,300 
 11/30/21	16:02:05	3.1574	3.16	3.17	12,100 
 11/30/21	16:01:54	3.16	3.16	3.17	2,200 
 11/30/21	16:00:08	3.16	3.15	3.18	2,200 
 11/30/21	16:00:08	3.16	3.15	3.18	1,400 
 11/30/21	16:00:01	3.16	3.15	3.18	808,800 
 11/30/21	16:00:00	3.16	3.15	3.16	798,826 
 11/30/21	15:59:53	3.15	3.15	3.16	1,800 
 11/30/21	15:59:53	3.15	3.15	3.16	2,600 
 11/30/21	15:59:53	3.15	3.15	3.16	500 
 
 
  
  
 DDD: 
 
 
 11/30/21	16:34:33	22.78	22.80	22.99	9,700 
 11/30/21	16:13:56	22.78	22.63	22.99	1,500 
 11/30/21	16:12:01	22.78	22.63	22.99	2,800 
 11/30/21	16:10:00	22.78	22.78	22.99	294,900 
 11/30/21	16:03:02	22.7805	22.47	22.99	2,300 
 11/30/21	16:02:59	22.7774	22.47	22.99	1,600 
 11/30/21	16:01:46	22.7186	22.47	22.99	900 
 11/30/21	16:01:41	22.78	22.47	22.99	1,300 
 11/30/21	16:01:11	22.78	22.47	22.99	500 
 11/30/21	16:00:27	22.78	22.47	22.99	800 
 11/30/21	16:00:27	22.78	22.47	22.99	1,900 
 11/30/21	16:00:27	22.78	22.47	22.99	600 
 11/30/21	16:00:27	22.78	22.47	22.99	1,500 
 11/30/21	16:00:27	22.78	22.47	22.99	900 
 11/30/21	16:00:27	22.78	22.47	22.99	1,600 
 11/30/21	16:00:07	22.78	22.47	22.99	500 
 11/30/21	16:00:02	22.78	22.47	22.85	900 
 11/30/21	16:00:02	22.78	22.47	22.85	294,900 
 11/30/21	16:00:02	22.78	22.47	22.85	294,900 
 11/30/21	16:00:02	22.78	22.47	22.85	294,219 
 11/30/21	15:59:57	22.80	22.77	22.80	5,400 
 11/30/21	15:59:56	22.80	22.77	22.80	1,300 
 11/30/21	15:59:56	22.80	22.77	22.80	7,184 
 
 
  
 DM: 
 
 
 11/30/21	16:34:19	6.52	6.46	6.51	21,500 
 11/30/21	16:30:31	6.52	6.46	6.51	900 
 11/30/21	16:22:33	6.48	6.46	6.49	4,800 
 11/30/21	16:10:00	6.52	6.46	6.52	373,500 
 11/30/21	16:09:57	6.52	6.46	6.52	500 
 11/30/21	16:09:57	6.52	6.46	6.52	500 
 11/30/21	16:09:57	6.52	6.46	6.52	500 
 11/30/21	16:09:10	6.52	6.46	6.55	2,700 
 11/30/21	16:06:18	6.52	6.40	6.52	800 
 11/30/21	16:02:53	6.52	6.40	6.52	2,100 
 11/30/21	16:02:50	6.5174	6.40	6.52	6,600 
 11/30/21	16:02:50	6.52	6.40	6.52	4,900 
 11/30/21	16:00:34	6.52	6.40	6.52	1,700 
 11/30/21	16:00:34	6.52	6.40	6.52	3,500 
 11/30/21	16:00:34	6.52	6.40	6.52	2,500 
 11/30/21	16:00:34	6.52	6.40	6.52	500 
 11/30/21	16:00:02	6.52	6.48	6.52	373,500 
 11/30/21	16:00:02	6.52	6.48	6.52	373,500 
 11/30/21	16:00:02	6.51	6.48	6.52	356,542 
 11/30/21	16:00:00	6.51	6.48	6.52	800 
 
 
  
 MRNA: 
 
 
 11/30/21	16:00:17	352.43	352.51	353.90	700 
 11/30/21	16:00:17	352.43	352.51	353.90	1,100 
 11/30/21	16:00:17	352.43	352.51	353.90	34,300 
 11/30/21	16:00:11	352.43	352.51	353.90	1,400 
 11/30/21	16:00:09	353.21	352.51	353.90	500 
 11/30/21	16:00:08	352.43	352.51	353.90	2,000 
 11/30/21	16:00:08	352.43	352.51	353.90	12,600 
 11/30/21	16:00:01	352.43	352.51	353.43	2,639,900 
 11/30/21	16:00:01	353.50 	352.51	353.43	2,638,091 
 11/30/21	15:59:59	353.06	352.90	353.48	2,100 
 11/30/21	15:59:59	352.82	352.90	353.48	5,283 
 11/30/21	15:59:59	353.00	352.70	353.50	3,834 
 
 
  
  
  
 Stocks without this pattern... 
  
 CGRN NVIV LQDA DTIL  OSIS  MARK CEMI RWLK 
  
  
  
 

                            

[XenaLives]

The U.S. Government - a terrorist organization.

http://edwardcurtin.com/u-s-terrorism-101-the-bert-sacks-story/

[XenaLives]

Ivermectin and COVID -

Aim: COVID-19 is currently the biggest threat to mankind. Recently, ivermectin (a US FDA-approved antiparasitic drug) has been explored as an anti-SARS-CoV-2 agent. Herein, we have studied the possible mechanism of action of ivermectin using in silico approaches. Materials & methods: Interaction of ivermectin against the key proteins involved in SARS-CoV-2 pathogenesis were investigated through molecular docking and molecular dynamic simulation. Results: Ivermectin was found as a blocker of viral replicase, protease and human TMPRSS2, which could be the biophysical basis behind its antiviral efficiency. The antiviral action and ADMET profile of ivermectin was on par with the currently used anticorona drugs such as hydroxychloroquine and remdesivir. Conclusion: Our study enlightens the candidature of ivermectin as an effective drug for treating COVID-19.
Keywords: : ivermectin, molecular docking, protease, replicase, SARS-CoV-2, spike glycoprotein

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7996102/

[XenaLives]

The punch line...

Not only is the Pfizer drug going to cost 10-20x more than Ivermectin,
Pfizer's allegedly "safe" protease inhibitor is fluorinated..

Yes, fluorine atoms are added and fluorine in antibiotics has been poisoning people for 30 years.

I was poisoned by Cipro on 2/25/18.

[XenaLives]

A Tale of Two Protease Inhibitors...

Protease inhibitors bind to a viral enzyme (called a protease), preventing the virus from replicating in the cell. Protease inhibitors have been effective at treating other viral pathogens such as HIV and hepatitis C virus, both alone and in combination with other antivirals. Currently marketed therapeutics that target viral proteases are not generally associated with toxicity and as such, this class of molecules may potentially provide well-tolerated treatments against COVID-19.

https://www.pfizer.com/news/press-release/press-release-detail/pfizer-initiates-phase-1-study-novel-oral-antiviral


Our government to spend billions on it up front, $300-$500 per course..

Pfizer, US in talks for 'multibillion-dollar' supply deal for COVID-19 pill: WaPo

https://www.fiercepharma.com/pharma/breaking-pfizer-line-for-5b-covid-pill-deal-report?oly_enc_id=8453B4904223J5S

[XenaLives]

Aussie news report banned from youtube...

The nurses are demonstrating and speaking the truth.

https://www.bitchute.com/video/zcijn6Tiwtr0/

[XenaLives]

Flourine - how can it be a a "harmful chemical" in cosmetics but a "breakthrough" in drugs?

The truth is that for some people fluorinated drugs kill or cause prolonged or permanent disability... but your doctor doesn't have a test to find out if you will be one of the unlucky victims.

The following cut and paste is straight from Google search Russian roulette anyone?

Fluorine atom drugs breakthrough - Hospital Healthcare Europehttps://hospitalhealthcare.com › news › fluorine-atom-d...
Aug 18, 2009 — Drug developers use the fluorine atoms to keep the body from breaking the drugs down too quickly, ensuring their effectiveness.

New molecule to improve pharmaceuticals draws inspiration ...https://www.europeanpharmaceuticalreview.com › news
May 16, 2018 — In the race to create more potent and stable medicines, scientists know that adding fluorine can improve drug molecules.

Manganese a promising new catalyst for drug synthesishttps://www.europeanpharmaceuticalreview.com › news
Oct 6, 2021 — Attaching negatively charged fluorine atoms to ketones helps direct the functional groups toward desired reactions when used in anti-cancer ...

Scientists find "harmful chemicals" in over 75% of makeuphttps://www.openaccessgovernment.org › harmful-che...
Jun 16, 2021 — Over three-quarters with high fluorine. The research team examined 231 cosmetic products purchased in the US and Canada for fluorine. They found ...

[XenaLives]

Excerpt from an article about BlackRock's way of doing business..

Hopefully Few has enough integrity to withstand this sort of onslaught.

There’s nothing I hate more than seeing big companies walk all over the little guy.

In the past few months, I’ve been investigating companies that look like they’re being manipulated. (It started with Gilead Sciences.) One thing I’ve found in common, is that lot of these manipulated companies have ties to BlackRock. (They’re usually a large stakeholder.)

What I think is happening is this:

BlackRock might be paying a troll factory to post negative comments about a stock. This creates negative sentiment which leads to selling. Which triggers algorithms and leads to more selling. Meanwhile, BlackRock might be shorting the stock. This sends the stock to all time lows, and then BlackRock probably buys all they can. Or in the case of GasLog, they buy the entire company.

The GasLog deal is the worst example of Wall Street fraud and treacherous behavior by management that I have ever seen in recent memory.

Management should be investigated for side deals. Why are they selling so cheap? What else are they getting? Were they promised cushy positions in the new GasLog? Spots on the board of directors of other companies?

This entire deal is completely nuts because it appears to be legal theft.

Everyone should protest this. Post comments on all the message boards. Contact the SEC. Contact your representatives. Contact news agencies.

If this buyout is allowed to proceed at this ridiculously low price, then no company is safe.

Otherwise, it becomes a case of, “First they came for GasLog and I said nothing…”

This era of investing will one day be regarded as the age of fraud. While I won’t be opening a position in GasLog, I am hoping that either the buyout is called off, or BlackRock is forced to pay a much higher price.

https://www.griproom.com/fun/blackrock-is-trying-to-steal-gaslog-and-why-you-should-care

[XenaLives]

BlackRock is Dirty -

see this video for facts:
https://www.reddit.com/r/amcstock/comments/m6gg20/mind_blown_an_amcgme_update_that_could_break_the/

Citadel Connect
As managing risk via off-exchange trading has become more important, institutional investors must connect to alternative sources of liquidity. Citadel Connect, our innovative Immediate-or-Cancel order (IOC) platform, is one of the fastest growing sources of off-exchange liquidity in the U.S. equities market, providing access to our principal liquidity for 8,000 exchange-listed securities. Citadel Connect enables us to provide investors, through their executing brokers, with efficient, reliable, and cost-effective access to our deep unique principal liquidity.

HOW WE DO IT
Citadel Connect aims to deliver extensive transaction cost savings, competitive fill rates, minimal market impact, and a fully customized trading experience. Our teams ensure seamless integration with this platform by using a diverse range of client trading infrastructures and routing technologies.

https://www.citadelsecurities.com/products/equities-and-options/

Citadel sees volume surge in its Citadel Connect dark pool
By John McCrank

4 MIN READ


NEW YORK, Feb 21 (Reuters) - Citadel Securities, one of the top market makers in U.S. stocks and listed stock options, said on Friday that volume on its off-exchange trading platform, Citadel Connect, has nearly tripled in the past year, making it one of the largest U.S. dark pools.

Dark pools, like exchanges, match buyers and sellers of stocks, but do so anonymously, and pre-trade information is not disclosed.

On an average day in January, 72 million shares traded through Citadel Connect, up from an average of 25 million a year earlier, the unit of Chicago-based hedge fund Citadel LLC said. It was the first time Citadel reported statistics for the venue.

Just a few weeks ago, the trading venue - where Citadel makes active retail orders it has taken the other side of available to institutional investors and other firms - did not even have a name, and was referred to as Citadel’s IOC Gateway, for “immediate or cancel.”

As a market maker, Citadel provides liquidity to the market by taking the other side of trades, executing around one of every four retail trades in U.S.-listed equities.

By making those retail trades, which were immediately executable, available to institutional traders and other market makers in its dark pool, it opens up liquidity that might not have been available otherwise, said Jamil Nazarali, head of Citadel’s retail and institutional market making division.

“You can’t have two market orders just hit. It’s like two bullets flying through - one of them has to be passive and the other active - that’s the only way you could cross,” he said.

“Instead of crossing the two market orders, we do the next best thing, we bridge the liquidity by buying from one and later selling to another.”

Nearly 40 percent of U.S. equity trades take place away from public exchanges in dark pools or through internalization, which is when a firm like Citadel takes the other side of a trade.

Dark pools began as a way for institutional firms to trade very large orders without tipping off the wider market, which could drive up the cost of their trade. But in recent years, the size of trades in dark pools has become smaller, comparable with exchanges, partly because many large orders are now broken into smaller pieces to be executed, and partly because more firms look to dark pools to avoid exchange fees.

Trades in Citadel Connect occur at the best bid and offer price offered by exchanges, though some occur at better prices. The average size of trades on the platform is around 240 shares, similar to the average on public exchanges.

There are around 45 U.S. dark pools and as many as 200 broker-dealer-run internalizers. Some of the largest dark pools include Credit Suisse’s Crossfinder and KCG Holdings’ Knight Link, which is comparable to Citadel Connect.

Very few stock orders that retail investors place with their brokers, such as Charles Schwab Corp, TD Ameritrade , or Fidelity, go through public stock exchanges, such as IntercontinentalExchange Group’s New York Stock Exchange. Instead, the brokers send the orders to other brokerage firms like or Citadel, or KCG, which trade against the incoming orders, and then send the leftovers to other internalizers, dark pools, or as a last resort, exchanges.

By doing this, the retail brokers not only avoid paying fees to the exchanges for active orders, but actually receive trading rebates from the off-exchange trading venues.

https://www.reuters.com/article/citadel-darkpool-idUSL2N0LQ17H20140221

[tootalljones]

this site should be a watering hole for independent minds and people who appreciate what is or was, America. Like spoiled brats, the invasion continues for the Oligarchs, per their plan. "Divide them, Scare them, and make what is left dependent on us." The communist playbook from way back. Read their literature. The literature of the communists is readily available. Read the guy Hillary did her senior thesis about, at Wellesly, a neighboring college of mine....which is not available to the public( I tried)...Rules for Radicals, another in a series of hundreds of socialists/communists/hating free speech tracts......A game plan for a gang takeover of governments..............their formula is quite good, CIA a chief practicioner of this plan, with foreign govs. now turning their talents inward.....We are in such deep sheat.

[tootalljones]

[tootalljones]

the human body is a miracle beyond human comprehension. Now or in a thousand years, or 10,000. He is top tier and confesses to this. The numbers which we can barely glimpse do not lie.

[tootalljones]

show me the bodies. Show me the mass graves, the gynamsiums full of hidden dead bodies. LOL....how many med charts have you audited? I bet zero. It is all a scam. You got your mask on now? I see that Nancy C and Dr. F take it off when the cameras are not rolling.

This is so scary that several avxl investors actually believe this nonsense...they insist on believing it! LOL

Should be a source of serious concern for the rational avxl investors.
Do you really want to have your money investors who are half nuts and hypochondriacs.?

They wanted to have everybody wear their ridicuous masks, but only libs wear them, and then they take them off when nobody is looking.
show me a single dead body of a single human under 70 who was healthy and who died from it?
Everybody with a sinus infection goes to the hospitals and are classified as covid, as the hospitals get the 15 grand or so in reiumbursements, the greedy docs making a fortune.

They hate ivermectin which can even kill another virus, the common cold.
They originally converted ships and set up military hospitals to take care of the bodies but had no no patients.
They are petrified if somebody went to a big hospital and audited the figures. Anybody with half a brain know the vac's are scam, dangerous, pincusioning stupid fearful people.

I have been in two ER rooms, major hospitals, twice post covid. Been there on average 4.5 hours...Nobody was there. These were two major hospitals, one of of which is one of the countries largest. The nurses were winking and noding and laughing. There was a rumor at one point in time, that they might be getting a single patient from 2 hours away, a half a million demo-graphic, btw...who "might" have covid, but the patient never showed up. Everybody, about a dozen nurses, various attendents are all pisseed off, and then about 5 minutes after that dissappointing news, they were all back to giggling like school girls....for 5 hours listening to them, I felt like I was at a sority house...It was hilarious. Because I was behind a curtained "room", I could not get to see how good looking they all were. If this is what a "pandemic looks like," I think we need more of them. A happier and more frivolous work force you have neve heard! Swear. I had like 4 nurses for me alone....a massivr vacant ER room.....
Where were the bodies? Such a scam............the children want to be afraid, like tellilng boogyman stories when you are kids.

show me the bodies, SHOW THE MASSIVE SQUARE ACRES OF GRAVES OF THE DEAD PEOPLE....EVERY DEAD PERSON WHO COUGHS BEFORE THEY CROAK IN A HOSPITAL IS CLASSIFIED AS COVID.....All these urban hospitals, jam packed with ghosts, but churning out these ccovid voters...LOL
Most of the docs, dripping in diamonds and cash, are all in on it, trying to keep it going with a straight face, their kids all in private schoools........We have tens of thousands of politiicans stat and federal, show me one of them who has croacked from covid. i would think by now we would have 300 to 500 of these highly visible politicins.

show me the audited medical cahrts. LOL...the feminine hypochonddriac population in america swears there are 500,000 bodies. Enouhhg for miles and miles of mass graves. Where are the graveyards? the body bags by the tens of thousands and really the hundreds of thousands of dead americans.? Fabricated statistics, of patient numbers and 'deaths." You will probably see a doc come on here now, and tell me I am wrong. Boy would I make the jury laugh at him on the stand.

The children so fearful of the truth, will remove this post. One thing about trying many hundreds of cases, is you get to meet a lot of "courthouse people." They will believe anything.

[XenaLives]

Increases in COVID-19 are unrelated to levels of vaccination across 68 countries and 2947 counties in the United States
S. V. Subramanian & Akhil Kumar
European Journal of Epidemiology (2021)Cite this article

CORRESPONDENCE
Published: 30 September 2021

....

Findings
At the country-level, there appears to be no discernable relationship between percentage of population fully vaccinated and new COVID-19 cases in the last 7 days (Fig. 1). In fact, the trend line suggests a marginally positive association such that countries with higher percentage of population fully vaccinated have higher COVID-19 cases per 1 million people. Notably, Israel with over 60% of their population fully vaccinated had the highest COVID-19 cases per 1 million people in the last 7 days. The lack of a meaningful association between percentage population fully vaccinated and new COVID-19 cases is further exemplified, for instance, by comparison of Iceland and Portugal. Both countries have over 75% of their population fully vaccinated and have more COVID-19 cases per 1 million people than countries such as Vietnam and South Africa that have around 10% of their population fully vaccinated.

https://link.springer.com/article/10.1007/s10654-021-00808-7

[XenaLives]

Facts about the Vax..

STORY AT-A-GLANCE
August 23, 2021, the U.S. Food and Drug Administration granted full approval to the COVID-19 mRNA injection developed by Pfizer/BioNTech, sold under the brand name Comirnaty, for use in people aged 16 and older
Normally, the FDA will hold a formal hearing and allow for public and expert input before a drug is moved from emergency use authorization to full approval but, in this instance, no such hearing was held
The notion that a “vaccine” that has killed more people in nine months than all other vaccines combined in three decades is considered safe stretches beyond the bounds of credulity and further undermines public trust in the FDA
The approval is based on six months’ worth of data from 44,047 people aged 16 and older. Half of them got the shots and half initially received a placebo. However, in early December 2020, Pfizer unblinded the control group and 93% of controls opted to get the real injection. This means we’ve had no control group since December 2020 and have nothing to compare the treatment group against
The FDA’s prescribing information for Comirnaty includes the risk of myocarditis and pericarditis, two types of heart inflammation that typically develop within seven days after the second injection
August 23, 2021, the U.S. Food and Drug Administration granted full approval1 to the COVID-19 mRNA injection developed by Pfizer/BioNTech, sold under the brand name Comirnaty, for use in people aged 16 and older.

It’s the fastest approval in history,2 granted less than four months after Pfizer filed for licensing May 7, 2021.3 It’s also based on just six months’ worth of data from 44,047 people aged 16 and older. Half of them got the shots and half initially received a placebo.

However, in the second week of December 2020, Pfizer unblinded the control group and 93% of controls opted to get the real injection4 rather than remain in the control group for the remainder of the trial, which is slated to continue for another two years.

Pfizer CEO Albert Bourla commented on the FDA’s approval, saying it “affirms the efficacy and safety profile of our vaccine,” and that he’s “hopeful this approval will help increase confidence in our vaccine …”5

According to STAT News,6 public health officials hope the approval “will persuade some people who remain hesitant about the vaccine to get the shot,” and will “make it easier for some public and private organizations to require vaccination.”

FDA Ditches Public Hearing, Circumventing Established Norms
Normally, the FDA will hold a formal hearing and allow for public and expert input before a drug is moved from emergency use authorization to full approval, but nothing is normal when it comes to COVID.

In this instance, no such hearing was held, and an FDA spokesperson called it unnecessary, because the public had been allowed to comment on all three COVID-19 jabs — Pfizer’s, Moderna’s and Johnson & Johnson’s — during a December 20, 2020, Vaccines and Related Biological Products Advisory Committee (VRBPAC) meeting. According to many, that isn’t good enough.7 As reported by The BMJ:8

“Kim Witczak, a drug safety advocate who serves as a consumer representative on the FDA’s Psychopharmacologic Drugs Advisory Committee, said the decision removed an important mechanism for scrutinizing the data.

‘These public meetings are imperative in building trust and confidence especially when the vaccines came to market at lightning speed under emergency use authorization,’ she said.

‘The public deserves a transparent process, especially as the call for boosters and mandates are rapidly increasing. These meetings offer a platform where questions can be raised, problems tackled, and data scrutinized in advance of an approval.’

Witczak is one of the more than 30 signatories of a citizen petition calling on the FDA to refrain from fully approving any COVID-19 vaccine this year to gather more data. She warned that without a meeting ‘we have no idea what the data looks like.’

‘It is already concerning that full approval is being based on 6 months’ worth of data despite the clinical trials designed for two years,’ she said. ‘There is no control group after Pfizer offered the product to placebo participants before the trials were completed.

Full approval of covid-19 vaccines must be done in an open public forum for all to see. It could set a precedent of lowered standards for future vaccine approvals.’”

Media Are Lying About Pfizer’s FDA Approval
Before we go any further, let’s clear up what the FDA actually approved, because they did not approve the Pfizer shot currently given. In the interview above, Dr. Robert Malone, the inventor of the mRNA vaccine platform, explains how we are being misled, yet again.

The injection that got the FDA approval is a Pfizer/BioNTech collaboration, to be sold under the brand name Comirnaty, and this injection is not currently available. Malone explains:

“The little trick that they’ve done here, is they’ve issued two separate letters for two separate vaccines. The Pfizer vaccine, which is what is currently available, is still under emergency use authorization and it still has the liability shield. Once again, the mainstream media have lied to you …

The product that’s licensed is the BioNTech product, which is substantially similar but not necessarily identical, called Comirnaty, and it’s not yet available. They haven’t started manufacturing it or labeling it. And that’s the one the liability waiver will no longer apply to.

So, the one that’s actually licensed is not yet available, and when it does become available it will no longer have the liability shield. In the interim, the one that does have the liability shield is the Pfizer product and that is what is currently available and it’s still under emergency use authorization.”

What this means is, if you want to get the licensed COVID shot, you have to wait. This also means that if employers demand that employees get vaccinated because there’s now a licensed COVID injection, employees should then demand to actually receive the FDA licensed Comirnaty,9 not the emergency use only10 Pfizer product that is currently being given.

FDA ‘Tricking Us Into Giving Up Our Right to Refuse’
Now, while the two products are not necessarily identical, the FDA in its infinite wisdom has decreed that the two can be used interchangeably, but their legal statuses, however, are not interchangeable. As explained by Robert F. Kennedy Jr. and Dr. Meryl Nass in a recent article:11

“There is a huge real-world difference between products approved under EUA compared with those the FDA has fully licensed. EUA products are experimental under U.S. law. Both the Nuremberg Code and federal regulations provide that no one can force a human being to participate in this experiment.

Under 21 U.S. Code Sec.360bbb-3(e)(1)(A)(ii)(III), ‘authorization for medical products for use in emergencies,’ it is unlawful to deny someone a job or an education because they refuse to be an experimental subject. Instead, potential recipients have an absolute right to refuse EUA vaccines. U.S. laws, however, permit employers and schools to require students and workers to take licensed vaccines.

EUA-approved COVID vaccines have an extraordinary liability shield under the 2005 Public Readiness and Preparedness Act. Vaccine manufacturers, distributors, providers and government planners are immune from liability.

The only way an injured party can sue is if he or she can prove willful misconduct, and if the U.S. government has also brought an enforcement action against the party for willful misconduct. No such lawsuit has ever succeeded.

The government has created an extremely stingy compensation program, the Countermeasures Injury Compensation Program, to redress injuries from all EUA products …

At least for the moment, the Pfizer Comirnaty vaccine has no liability shield. Vials of the branded product, which say “Comirnaty” on the label, are subject to the same product liability laws as other U.S. products …

Just as with Ford’s exploding Pinto, or Monsanto’s herbicide Roundup, people injured by the Comirnaty vaccine could potentially sue for damages. And because adults injured by the vaccine will be able to show that the manufacturer knew of the problems with the product, jury awards could be astronomical.

Pfizer is therefore unlikely to allow any American to take a Comirnaty vaccine until it can somehow arrange immunity for this product.

Given this background, the FDA’s acknowledgement in its approval letter that there are insufficient stocks of the licensed Comirnaty, but an abundant supply of the EUA Pfizer BioNTech jab, exposes the “approval” as a cynical scheme to encourage businesses and schools to impose illegal jab mandates.

The FDA’s clear motivation is to enable Pfizer to quickly unload inventories of a vaccine that science and the Vaccine Adverse Events Reporting System have exposed as unreasonably dangerous, and that the Delta variant has rendered obsolete.

Americans, told that the Pfizer COVID vaccine is now licensed, will understandably assume COVID vaccine mandates are lawful. But only EUA-authorized vaccines, for which no one has any real liability, will be available during the next few weeks when many school mandate deadlines occur.

The FDA appears to be purposefully tricking American citizens into giving up their right to refuse an experimental product … Here’s what you need to know when somebody orders you to get the vaccine: Ask to see the vial. If it says ‘Comirnaty,’ it’s a licensed product.

If it says ‘Pfizer-BioNTech,’ it’s an experimental product, and under 21 U.S. Code 360bbb, you have the right to refuse. If it comes from Moderna or Johnson & Johnson (marketed as Janssen), you have the right to refuse.

The FDA is playing bait and switch with the American public — but we don’t have to play along. If it doesn’t say Comirnaty, you have not been offered an approved vaccine.”

Approval by Captured Agency Hardly Affirms Safety
While the notion of full approval might sway some fence-sitters, especially if they don’t understand that the licensed product is not what you get if you get a Pfizer shot right now, it’s unlikely to influence those who have kept an eye on the skyrocketing number of adverse event reports logged into the U.S. Vaccine Adverse Events Reporting System (VAERS).

As of August 13, 2021, VAERS had logged 595,620 adverse events following COVID injection, including 54,142 hospitalizations and 13,608 deaths.12 While these numbers are completely unheard of — with reported deaths from COVID-19 shots exceeding the reported death rate of more than 70 vaccines combined over the past 30 years — they may still be just the tip of the iceberg.

Previous investigations have shown VAERS reports account for a mere 1%13,14 to 10%15 of all vaccine-related injuries, which means the death toll from these jabs may be in the six-digits already.

The notion that a “vaccine” that has killed more people in nine months than all other vaccines combined in three decades is considered safe really stretches the bounds of credulity. It’s simply not believable, and to many simply reaffirms the suspicion that the FDA is a captured agency working for the benefit of Big Pharma rather than safeguarding the public from dangerous drugs.

As noted by a commenter on BMJ associate editor Peter Doshi’s article “Does the FDA Think These Data Justify the First Full Approval of a COVID-19 Vaccine?” republished by The Defender:16

“The Fraud and Death Administration has really outdone itself this time. Owned by pharma, serving pharma, to the extreme detriment to humanity. They deserve to be shuttered permanently, they are an organization of criminals.”

Risk of Heart Inflammation Acknowledged
The FDA didn’t go so far as to give the Pfizer shot a completely clean bill of health, however. As reported by STAT News:17

“The FDA’s prescribing information for the vaccine includes its associated risk of myocarditis and pericarditis, two types of heart inflammation that have appeared rarely among people who’ve received the mRNA vaccines, mostly within seven days after the second shot, health officials said. Men under 40 appear to be at higher risk than women and older men, with the highest observed risk in boys age 12 to 17.”

According to the Centers for Disease Control and Prevention, As of August 18, 2021, VAERS had received 1,339 reports of myocarditis or pericarditis in people under the age of 30 following COVID injection, with a majority of these cases being associated with the Pfizer shot.18

Pfizer’s new Comirnaty package insert19 also clearly states at the top of its first page under “Warnings and Precautions” that “postmarketing data demonstrate increased risk of myocarditis and pericarditis, particularly within seven days of the second dose.”

Then, under Section 5.2 of the insert, Pfizer has added an entire section explaining the details of those adverse effects, and directing readers to a CDC webpage20 that addresses those effects in adolescents and young adults.

Heart Inflammation Study Won’t End Until 2025
In its approval letter for Comirnaty,21 the FDA orders Pfizer/BioNTech to conduct research to investigate the risk of inflammation in and around the heart, as voluntary reporting mechanisms are insufficient:

“We have determined that an analysis of spontaneous postmarketing adverse events reported under section 505(k)(1) of the FDCA will not be sufficient to assess known serious risks of myocarditis and pericarditis and identify an unexpected serious risk of subclinical myocarditis.

Furthermore, the pharmacovigilance system that FDA is required to maintain under section 505(k)(3) of the FDCA is not sufficient to assess these serious risks.

Therefore, based on appropriate scientific data, we have determined that you are required to conduct the following studies: 4. Study C4591009, entitled ‘A Non-Interventional Post-Approval Safety Study of the Pfizer-BioNTech COVID-19 mRNA Vaccine in the United States,’ to evaluate the occurrence of myocarditis and pericarditis following administration of COMIRNATY.”

The FDA accepted Pfizer’s suggested timetable for the post-approval study to evaluate incidence of heart and heart sack inflammation, which includes the submission of an interim report at the end of October 2023, a study completion date of June 30, 2025, and submission of a final report October 31, 2025.

Modern-Day Child Sacrifice?
The notion that the current Pfizer shot or the BioNTech product, Comirnaty, are “safe” is rather ludicrous in light of all this, and the idea that the FDA is even considering approving the shot for children as young as 1222 — and are running trials on babies — is completely incomprehensible. Even worse, Fauci is pushing for infant approval by the end of the year.23

The myocarditis study for Comirnaty (which may or may not be as dangerous as the current Pfizer shot) won’t be completed until four years from now, yet they see it fit to give this experimental injection to every last child in the United States? What are they thinking? Is it really wise to trade the risk of flu-like illness for heart damage? From the start of this pandemic, children have proven very resistant to SARS-CoV-2 infection and rarely ever suffer any significantly ill effects.

As reported by NPR,24 Pfizer’s youth trial, which includes children between the ages of 6 months and 11 years, doesn’t even test “to see whether the vaccine actually prevents children from getting sick.” Instead of assessing actual symptoms, the trial “will look at their blood to see if they are making the kinds of antibodies that have been shown to prevent disease.”

In other words, all they’re looking for is the antibody against the synthetic spike protein your body produces. But that antibody is not the best way to assess protection, as the protection is very narrow. Actual viruses contain several different proteins against which your body produces both antibodies and memory T cells when you’re infected naturally.

This is why natural immunity is far more robust and long-lasting, and why the claim that vaccine-induced protection is superior to natural immunity is false. In my view, experimenting on children and not even doing a comprehensive job of it is simply unconscionable.

Do Data Justify Full Approval of Pfizer’s COVID Jab?
In the morning of August 23, 2021, mere hours before the FDA announced its approval of the Pfizer shot, Doshi published a BMJ blog questioning whether available data could really support full approval. He wrote:25

“On 28 July 2021, Pfizer and BioNTech posted updated results for their ongoing phase 3 covid-19 vaccine trial. The preprint came almost a year to the day after the historical trial commenced, and nearly four months since the companies announced vaccine efficacy estimates ‘up to six months.’

But you won’t find 10 month follow-up data here. While the preprint is new, the results it contains aren’t particularly up to date. In fact, the paper is based on the same data cut-off date (13 March 2021) as the 1 April press release, and its topline efficacy result is identical: 91.3% … vaccine efficacy against symptomatic covid-19 through ‘up to six months of follow-up.’

The 20 page preprint matters because it represents the most detailed public account of the pivotal trial data Pfizer submitted in pursuit of the world’s first ‘full approval’ of a coronavirus vaccine from the Food and Drug Administration. It deserves careful scrutiny.”

Doshi points out that while Pfizer has touted a 95% efficacy rate, and even higher against severe disease, this refers to relative risk reduction, not absolute risk reduction, which is actually an insignificant 0.7%26 to 0.84%.27 Moreover, “measuring vaccine efficacy two months after dosing says little about just how long vaccine-induced immunity will last,” Doshi says.

6-Month Preprint Showed Evidence of Waning Immunity
Rapidly waning immunity is the proverbial elephant in the room, according to Doshi, who points to Israeli data showing Pfizer’s shot went from a 95% effectiveness at the outset, to 64% in early July 2021 and 39% by late July, when the Delta strain became predominant. “This is very low,” Doshi says, pointing out that the FDA’s expectation for any vaccine is an efficacy rate of at least 50%.

Waning efficacy has the potential to be far more than a minor inconvenience; it can dramatically change the risk-benefit calculus. ~ Peter Doshi
The FDA cannot claim it doesn’t know the protection offered is pathetically short, as Pfizer’s preprint, which contained six months’ worth of data, showed evidence of rapidly waning immunity as early as March 13, 2021.

By the fourth month into the trial, efficacy had dropped from 96% to 90%, and one month after that, it was down to 84%. Curiously, while Pfizer had this data in April 2021, they didn’t publish it until the end of July 2021. Still, that’s what the FDA is basing its decision on.

What’s more, this rapid drop in effectiveness could hardly be due to the emergence of the Delta variant, Doshi adds, because 77% of trial participants were in the U.S., where the Delta variant didn’t become established until months after the data cut-off date.

“Waning efficacy has the potential to be far more than a minor inconvenience; it can dramatically change the risk-benefit calculus,” Doshi writes.28 “And whatever its cause — intrinsic properties of the vaccine, the circulation of new variants, some combination of the two, or something else — the bottom line is that vaccines need to be effective.

Until new clinical trials demonstrate that boosters increase efficacy above 50%, without increasing serious adverse events, it is unclear whether the 2-dose series would even meet the FDA’s approval standard at six or nine months.”

There’s NO Control Group in This Mass Experiment
Making matters even worse, Pfizer, like all other COVID jab developers, went ahead and eliminated their control groups at the end of 2020. So, we’re figuratively flying blind, having nothing to compare the vaccinated treatment group against.

This is a recipe for disaster, as it effectively hides side effects. If large numbers of people suddenly start developing a health problem, it can simply be written off as a new normal and/or can be blamed on some other environmental factor. Doshi comments on how this decision impacts our ability to evaluate any data coming out of these trials:29

“Despite the reference to ‘six month safety and efficacy’ in the preprint’s title, the paper only reports on vaccine efficacy ‘up to six months,’ but not from six months.

This is not semantics, as it turns out only 7% of trial participants actually reached six months of blinded follow-up (‘8% of BNT162b2 recipients and 6% of placebo recipients had ≥6 months follow-up post-dose 2.’) …

This all happened because starting last December, Pfizer allowed all trial participants to be formally unblinded, and placebo recipients to get vaccinated. By 13 March 2021 (data cut-off), 93% of trial participants (41,128 of 44,060 …) were unblinded, officially entering ‘open-label followup’ …

So despite this preprint appearing a year after the trial began, it provides no data on vaccine efficacy past six months, which is the period Israel says vaccine efficacy has dropped to 39%.

It is hard to imagine that the <10% of trial participants who remained blinded at six months (which presumably further dwindled after 13 March 2021) could constitute a reliable or valid sample to produce further findings.”

With the approval of Comirnaty, a formal package insert30 has been released, and in section 6.1, they clearly state they’ve not had placebo participants since December 2020, not even among teenagers:31

“Section 6.1 — Upon issuance of the Emergency Use Authorization (December 11, 2020) for COMIRNATY, participants were unblinded to offer placebo participants COMIRNATY. Participants were unblinded in a phased manner over a period of months to offer placebo participants COMIRNATY.”

While a formal package insert now exists for Pfizer’s mRNA shot, the Centers for Disease Control and Prevention will not issue Vaccine Information Statements (VIS) for it, but will continue to use online fact sheets. (The use of online fact sheets is why all package inserts for the COVID shots have been completely blank.)

If You’re ‘Vaccinated’ You May Be High-Risk for COVID
As discussed in yesterday’s lead article (August 30, 2021), data are now mounting showing people over the age of 50 who are “fully vaccinated” actually make up the bulk of COVID-19 related hospitalizations and deaths in that age group. One possible explanation for this is that antibody dependent enhancement is afoot, which makes people more prone to serious illness rather than less.

To be on the safe side, I recommend considering yourself “high-risk” for severe COVID if you’ve received one or more shots, and implement known effective treatment at the first sign of a respiratory infection.

Options include the Zelenko protocol,32 the MATH+ protocols33 and nebulized hydrogen peroxide, as detailed in Dr. David Brownstein’s case paper34 and Dr. Thomas Levy’s free e-book, “Rapid Virus Recovery.” Whichever treatment protocol you use, make sure you begin treatment as soon as possible, ideally at first onset of symptoms.

https://www.technocracy.news/the-curious-case-of-fdas-approval-of-comirnaty/?fbclid=IwAR1_fzfRdcJaL_YgUAooUAicvQJESGyyV48LqfS75T_wkLPz-iksrMR-TwU

[XenaLives]

An expert on COVID vax deaths and autopsies..

https://rumble.com/vm7z6l-autopsy-results-of-the-vaccinated-must-see.html

[XenaLives]

Why the U.S. had the highest COVID death rate...

https://www.bitchute.com/video/IC2LQQpieYl6/

[XenaLives]

Here is the caption - I still had a screen open:

15th September, 2021 - Albert Spence, a 31-year pulmonary nurse veteran, addresses the South Carolina Medical Affairs Committee and explains how he came to realize that he was aiding and abetting the demise of patients under his care, due to the change in Covid policy - specifically

He clearly described murder of early COVID patients through medical malpractice. He said he felt like "opened the doors to the gas chambers at Auschwitz" (from memory, may not be a verbatim quote.

There but for the grace of G-d go I. I made four trips to the ER in late 2019. They could find noting wrong. Self medication with NAC and other supplements kept me alive.

In Edit - found it on bitchute.

https://www.bitchute.com/video/mYf2mTn1PWuy/

[chickenvestor]

Need to find another platform. YouTube has taken it down. I wish their censorship could be stopped.

[XenaLives]

Must see Nurse testimony...

https://www.youtube.com/watch?v=wbfWBrukpLc

[XenaLives]

The New Moonshot Technologies
Resources
BofA Global Research released a 152-page research report identifying 14 “radical technologies that could change our lives and accelerate the impact of global megatrends.” The technologies have a $330B market size today that could grow to $6.4T by the 2030s, strategists led by Haim Israel say. “These moonshots could transform and disrupt multiple industries, contributing to the next big cycle of technology-driven growth.” Israel says. The 14 are:



6G: “The next generation of telecom networks will be needed in less than a decade as data continues to grow exponentially and 5G reaches its upper limit capacity.”

Brain Computer Interfaces: “As we reach a point where humans are unable to keep up with computers and AI, brain computer interfaces could help ‘level up’ humans with computers. Shorter term, brain computer interfaces hold solutions for paralyzed individuals and promise a new wave of innovation in gaming.”

Emotional Artificial Intelligence: Also “known as 'Affective Computing' and 'Cognitive Computing' (it) is designed to capture, analyze and respond to human emotions and simulate human thoughts. EAI can potentially collect, analyze and respond to completely new varieties of data and situations and predict or simulate human thought, leading people to take action.”

Synthetic Biology: “At its core, 'synbio', as the field is commonly referred to, takes advantage of the vast diversity of nature to make biomolecules that traditional chemistry cannot.”

Immortality: “Traditionally, aging has not been viewed as a disease that can be treated but this is changing. Actors in this space are increasingly looking to tackle the hallmark of aging via pathways such as genomic instability, telomere attrition, mitochondrial dysfunction, and cellular senescence among others.”

Bionic humans: “This could be invasive (e.g. implants) or non-invasive (e.g. exoskeleton). Biohacking is also an associated field which is essentially applying DIY biology to boost oneself e.g. RFID chip in hand for contactless payments.”

eVTOL: “Electrical vertical take-off and landing vehicles that could provide an alternative mobility transportation solution to outdated infrastructure and overly stressed roads in urban settings.”

Wireless Electricity: “As the IoT takes off, automating and creating near continuous charging solutions could provide convenience for consumers, while solving charging problems for the rollout of EVs and secure electricity supplies for remote communities.”

Holograms: “A technology capable of creating a simulated environment through light imagery projections that will allow everyone to come together in one virtual room, without having to leave their physical location.”

Metaverse: “A future iteration of the Internet, made up of persistent, shared, 3D-shared spaces linked into a virtual universe. It could comprise countless persistent virtual worlds that interoperate with one another, as well as the physical world and transforming markets such as gaming, retail, entertainment etc.”

Nextgen Batteries: “Whilst lithium batteries are the major EV technology, this does not necessarily need to stay true with alternatives such as solid state, vanadium flow, sodium ion etc provide promising additional attributes.”

OceanTech: “It seeks to answer: ‘How do we increase sustainability of the ocean economy while harnessing its benefits?’ Solutions could include ocean energy, land based aquaculture, and precision fishing using AI.”

Green Mining: “Transitioning away from a carbon-intensive economy will mean moving to a metal-intensive one. Green mining solutions like deep-sea mining, agromining, mining of wastewater and asteroid mining could provide less polluting and destructive solutions as the green economy’s thirst for metals grows.”

Carbon Capture and Storage: “All current zero-carbon pathways require some form of CO2 removal. CCS, alongside other geoengineering solutions, could act as part of the solution with long-term permanent removal of CO2 vs afforestation.”

https://assets.bwbx.io/images/users/iqjWHBFdfxIU/izsrvpss9WiY/v0/-1x-1.png

Lower lifespan: The lifespan of S&P 500 incumbents is shortening and by 2027 components could last just 12 years before being replaced, BofA says. For Next Tech to succeed, first the innovation must have the potential to be economical, then it must solve a key problem or improve quality of life, and finally, there must be government support in some way. Risks to the 14 ideas include the tech not being commercially scalable, prohibitive costs outweighing the benefits and regulation limiting applicability.

https://www.reddit.com/r/stocks/comments/ppcbyw/the_new_moonshot_technologies/

[XenaLives]

Another fraudulent drug approval:

[XenaLives]

What VAERS data reveals:

https://www.youtube.com/watch?v=WFph7-6t34M&t=14993s

[nygirl]

ty Xena!!!