Coronavirus

[Dachsie]

Dachsie comments:

There are several fairly recent postings in this thread regarding "hydra vulgaris parasites" found to be present in the mRNA vaccine contents viewed under a microscope by Dr. Carrie Madeg.

https://ambassadorlove.wordpress.com...human-cloning/
November 1, 2021 by Dr. Ariyana Love
Transgenic Hydras & Parasites A Biological Weapons System For Rapid Human Cloning
By Dr. Ariyana Love
The transhumanist dystopian nightmare we find ourselves in is taking a new turn with the shocking discovery of Hydra Vulgaris and PARASITES in the so-called Covid-19 “vaccines”.
Dr. Carrie Madej revealed her Hydra findings on the Stew Peter’s Show on September 29th, 2021, followed by Dr. Zandre Botha’s stunning discovery of microscopic, self-assembling medical devices in the blood of her vaxxed patients. The red blood cells are dangerously deformed and coagulated, things she says she’s never seen before in her 15 years as a blood doctor.




https://thelightinthedarkplace.files...nism.jpg?w=816

Source:
https://thelightinthedarkplace.wordp...ology-in-vaxx/
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Here is the thumbnail photo that goes with this posting's video.

https://static-3.bitchute.com/live/c...lR_320x180.jpg






https://www.bitchute.com/video/tWzQlrj0IUdu/


URGENT Hydras CONFIRMED as AI Remote Control GO Delivery Devices

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First published at 14:08 UTC on November 14th, 2021.

#russbrown #hydra #grapheneoxide

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SixthSense

SixthSense

34041 subscribers

MIRRORED FROM:
RussBrown: https://www.bitchute.com/channel/russbrown/
https://www.bitchute.com/video/PfysbJOmzNwR/
SKIP TO 3 MIN 20
HYDRA are remote GO ĺnano delivery devices

Game changing BOMBSHELL info.

In this 2020 vid from the Economist (who alway…
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[Dachsie]

https://europepmc.org/article/med/34601006


A Report on Myocarditis Adverse Events in the U.S. Vaccine Adverse Events Reporting System (VAERS) in Association with COVID-19 Injectable Biological Products.
Rose J1,
McCullough PA1
Author information

Current Problems in Cardiology, 30 Sep 2021, :101011
DOI: 10.1016/j.cpcardiol.2021.101011 PMID: 34601006 PMCID: PMC8483988

ReviewFree to read & use
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Abstract
Following the global rollout and administration of the Pfizer Inc./BioNTech BNT162b2 and Moderna mRNA-1273 vaccines on December 17, 2020, in the United States, and of the Janssen Ad26.COV2.S product on April 1st, 2021, in an unprecedented manner, hundreds of thousands of individuals have reported adverse events (AEs) using the Vaccine Adverse Events Reports System (VAERS). We used VAERS data to examine cardiac AEs, primarily myocarditis, reported following injection of the first or second dose of the COVID-19 injectable products. Myocarditis rates reported in VAERS were significantly higher in youths between the ages of 13 to 23 (p<0.0001) with ∼80% occurring in males. Within 8 weeks of the public offering of COVID-19 products to the 12-15-year-old age group, we found 19 times the expected number of myocarditis cases in the vaccination volunteers over background myocarditis rates for this age group. In addition, a 5-fold increase in myocarditis rate was observed subsequent to dose 2 as opposed to dose 1 in 15-year-old males. A total of 67% of all cases occurred with BNT162b2. Of the total myocarditis AE reports, 6 individuals died (1.1%) and of these, 2 were under 20 years of age - 1 was 13. These findings suggest a markedly higher risk for myocarditis subsequent to COVID-19 injectable product use than for other known vaccines, and this is well above known background rates for myocarditis. COVID-19 injectable products are novel and have a genetic, pathogenic mechanism of action causing uncontrolled expression of SARS-CoV-2 spike protein within human cells. When you combine this fact with the temporal relationship of AE occurrence and reporting, biological plausibility of cause and effect, and the fact that these data are internally and externally consistent with emerging sources of clinical data, it supports a conclusion that the COVID-19 biological products are deterministic for the myocarditis cases observed after injection.

[Dachsie]

https://static-3.bitchute.com/live/c...Jo_320x180.jpg

https://www.bitchute.com/video/STtAt9L1P2Jo/


PT8 Children Covid-19 Vaccine CDC Authorized Pfizer For Kids Ages 5to11 15 Million Shots Ready

21:20 video runtime

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First published at 13:22 UTC on November 12th, 2021.

#covid-19 #coronavirus #pandemic

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AllTheWorldsAStage

Alltheworldsastage

2548 subscribers

PT8 Children Covid-19 Vaccine CDC Authorized Pfizer For Kids Ages 5to11 15 Million Shots Ready

[Dachsie]

This applies to the J & J vaccine.





https://www.bitchute.com/video/qY2D2FfCtMRB/


Dr. Ariyana Love - Ebola Virus in Covid Shots!!!

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First published at 17:10 UTC on November 14th, 2021.

#covid #vaccine #vaccines

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FreiheitsFreund

FreiheitsFreund

24584 subscribers

Video taken from Covid Vaccine Injuries. - Paving the way for deadly Marburg Virus scare.

Telegram: https://t.me/covidvaccineinjuries

[Dachsie]

https://www.youtube.com/watch?v=_LzcGOjDl8Q



8:03 video runtime

Gravitas: Was Pfizer's Covid-19 vaccine trial "compromised"?

Nov 5, 2021

WION

Was Pfizer's Wuhan Virus vaccine trial compromised? A whistleblower who worked for the company hired to run the trial spotted several lapses. She was allegedly fired after she sent a complaint to US FDA. Palki Sharma brings you a report.

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https://www.lifesitenews.com/news/pf...dical-journal/

Tue Nov 2, 2021 - 8:43 pm EDT

(LifeSiteNews) — A former regional director for a private clinical research company provided evidence that her prior employer falsified data, unblinded trial participants, and neglected the timely follow-up of subjects experiencing adverse events as they conducted a Pfizer COVID-19 vaccine trial in the fall of 2020.

According to a report from the BMJ, Brook Jackson, a “trained clinical trial auditor” with more than “15 years’ experience in clinical research coordination and management,” worked for Ventavia Research Group of Texas for two weeks in September 2020. After repeatedly alerting her employer of the overwhelming problems in quality control of the trial, she emailed a complaint to the U.S. Food and Drug Administration (FDA) and was fired by her employer later the same day.

Paul D. Thacker of the BMJ wrote that his medical journal is in possession of “dozens of internal company documents, photos, audio recordings, and emails” provided by Jackson. One photo shows “vaccine packaging materials with trial participants’ identification numbers written on them left out in the open, potentially unblinding participants.”

“Blinding” is an important aspect for the integrity of randomized control trials. It safeguards against bias in those conducting the trial when collecting data on participants whose status of receiving the intervention or a placebo remains unknown. For example, research organizations may have financial incentives to produce an outcome favorable to their client; in this case, Pfizer, and their knowledge of trial participants’ status may bias them in how they collect data.

Further, according to the report, this unblinding may have occurred on a much wider scale as “drug assignment confirmation printouts were being left in participants’ charts, accessible to blinded personnel.”

Such widespread issues were apparently known by Ventavia management, according to an audio recording of a meeting with Jackson and two directors. One executive is heard lamenting that they were not able to quantify the numbers and types of errors they were uncovering in their quality control process. “In my mind, it’s something new every day,” the executive states. “We know that it’s significant.”

In addition, the neglect of trial subjects experiencing adverse reactions from the injections was an omission that earned Ventavia an emailed reprimand from ICON, a “contract research organization” partnering with Pfizer on the trial.

The September 2020 email reminded Ventavia, “The expectation for this study is that all queries are addressed within 24hrs.” The contractor went on to highlight more than 100 instances where queries were more than three days old. According to Thacker, “Examples included two individuals for which ‘Subject has reported with Severe symptoms/reactions … Per protocol, subjects experiencing Grade 3 local reactions should be contacted. Please confirm if an UNPLANNED CONTACT was made and update the corresponding form as appropriate.’”

In Jackson’s September 25 email to the FDA, she listed many concerns based on her experience with the Pfizer trial. According to the BMJ, these included:

Participants placed in a hallway after injection and not being monitored by clinical staff
Lack of timely follow-up of patients who experienced adverse events
Protocol deviations not being reported
Vaccines not being stored at proper temperatures
Mislabeled laboratory specimens, and
Targeting of Ventavia staff for reporting these types of problems.

Other documents provided by Jackson indicate that significant problems had been present for many weeks before her arrival. In a list of “action items” distributed among Ventavia leadership in early August 2020, one executive identifies three staff members with whom to “Go over e-diary issue/falsifying data, etc.” One of these was “verbally counseled for changing data and not noting late entry,” according to the note.

Former colleagues of Jackson have corroborated her story. One previous executive who was in the recorded meeting referenced above apologized to her in a June text message stating “everything that you complained about was spot on.”

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Two others, who spoke to BMJ anonymously out of fear of compromising future job prospects, each “confirmed broad aspects of Jackson’s complaint.” Thacker wrote how one of these individuals said “she had worked on over four dozen clinical trials in her career, including many large trials, but had never experienced such a ‘helter-skelter’ work environment as with Ventavia on Pfizer’s trial.”

“I’ve never had to do what they were asking me to do, ever,” she told BMJ. “It just seemed like something a little different from normal — the things that were allowed and expected.”

She also reported that Ventavia was at times short staffed and unable to test all of the trial participants who reported symptoms for COVID-19, to confirm infection, even though this was “the trial’s primary endpoint.” While such neglect may likely skew infection rate data for vaccine recipients, Thacker does report that an August 2021 FDA memorandum “states that across the full trial (44,000 participants), swabs were not taken from 477 people with suspected cases of symptomatic covid-19.”

However, in regard to this Pfizer research trial conducted by Ventavia, this same employee quoted above concluded, “I don’t think it was good, clean data.” In fact, “it’s a crazy mess.”
Tagged as

bmjFdaPfizer Covid-19 vaccineventavia research groupWhistleblower

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https://www.bmj.com/content/375/bmj....campaign=usage


Covid-19: Researcher blows the whistle on data integrity issues in Pfizer’s vaccine trial
BMJ 2021; 375 doi: https://doi.org/10.1136/bmj.n2635 (Published 02 November 2021) Cite this as: BMJ 2021;375:n2635

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Dachsie comments:

More Pfizer corruption. Subcontractor corruption of Ventavia Research Group of Texas where Brook Jackson blew the whistle and was promptly fired.

[Dachsie]

https://www.youtube.com/watch?v=1uh-ZGDx0P4



1:47 video runtime

They Lied to Us About Vaccine Mandates
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Nov 8, 2021
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Dr. Scott Jensen
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They lied to us about mandates.

Becoming a health freedom sanctuary state is the only path forward! Tim Walz has not proven he can take on his own party when his own party is WRONG. The mandates are unconstitutional, and our government should be challenging them! Moms and dads expect it!

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[Dachsie]

This Infowars radio show host was denied medical service of monclonal antibodies treatment for "Covid" at an unnamed infusion center ? because he is not Black or Hispanic.

Twitter link below contains video on that denial transaction.

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https://nationalfile.com/texas-radio...k-or-hispanic/

TEXAS: Radio Host Refused Monoclonal COVID Treatment Because He’s Not ‘Black Or Hispanic’

"Race and gender extremism isn't just in gender study classes or elementary schools, it's being taught in Medical schools and is having real-world effects."
Jack Hadfield by Jack Hadfield
November 13, 2021




Harrison Hill Smith, a Texas radio host, was denied monoclonal antibody treatment for COVID because he is white, not black or Hispanic.

Smith, who presents the American Journal on the InfoWars network, tweeted on Saturday that he was denied receiving monoclonal antibody treatment for COVID because he was white, adding that such treatment was only available “for blacks and Hispanics,” which he described as being “fucking insane.”

Despite some initial skepticism from some leftists, Smith produced a video clearly showing medical staff declaring that the only reason for his rejection was his ethnicity.

Dave Reilly, an America First commentator and former Republican candidate, was able to corroborate Smith’s story via a phone call with the Texas State Infusion Hotline. “There’s eligibility criterias that we go by, and African American and Hispanic are high risk ethnicity groups, so that would be a qualifier,” the hotline staff member told Reilly, saying that “people with a BMI of 25 or higher, people who are 65 years of age or up, or high risk ethnicity groups can get it.”

“So if you are a healthy, in-shape, Caucasian, and you show up, you are not gonna get an infusion?” Reilly asked the phone representative. “Based on the criteria that we go by right now, that is correct,” they confirmed.

Tweet

https://twitter.com/Harrison_of_TX/s...or-hispanic%2F

Harrison Hill Smith
@Harrison_of_TX
"State Infusion Hotline"

1-800-742-5990

Ask them yourself.
10:03 AM · Nov 13, 2021·Twitter for Android
491
Retweets
17
Quote Tweets
2,870
Likes


This Infowars radio show host was denied medical service of monclonal antibodies treatment for "Covid" at an unnamed hospital because he is not Black or Hispanic.

Twitter link below contains video on that denial transaction.



https://twitter.com/Harrison_of_TX/s...or-hispanic%2F

Harrison Hill Smith
@Harrison_of_TX
Denied medical service because of my race.
12:39 PM · Nov 13, 2021·Twitter for Android



Dave Reilly

https://twitter.com/realDaveReilly/s...or-hispanic%2F

Call the Texas Infusion Hotline

and the video records the conversation.

Apparently this Infusion hotline group - name ? --

has qualifying guidelines for who can receive this infusion treatment of monoclonal antibodies.

The person on the phone said Hispanic and Black are recognized as "high risk ethnicity groups" and are more vulnerable population so these groups of given highest priority in being allowed to have the antibody treatment.

Something does not seem right about this. Maybe more facts will come out later.

I assume that Harrison Hill Smith, would not have presented at the infusion center if he did not have a prescription for the infusion from his attending medical doctor. I thought that was enough to warrant receiving the treatment. I did not think that a company's "qualifying criteria" or whatever they call them would overrule the doctor's order.

Something about his seems crookeder than a dog's hind leg, but hey, this is Texas.

[Dachsie]

Dachsie comment:

Shame on the
Texas Department of State Health Services
for secretly approving these unapproved unauthorized experimental "Covid-19" vaccines for children.
https://dshs.texas.gov/



https://dshs.texas.gov/images/HHSDSHS-Logo.png

https://dshs.texas.gov/contact.shtm

General Inquiries and Consumer Complaints
• Email: customer.service@dshs.texas.gov
• Phone: 512-776-2150 or 1-888-963-7111, ext. 2150; TDD: 1-800-735-2989
• Mail:
Department of State Health Services
attn: Customer Service Coordinator
PO Box 149347, MC-1913
Austin, Texas 78714-9347

I ask that everyone check and see what your own respective state health agencies have done in this regard and complain loudly.

And parents with young children in public schools don't get a pass for being trusting and uninformed about the serious harm that they are passively causing for their children.

John 16:2

They will put you out of the synagogues: yea, the hour cometh, that whosoever killeth you, will think that he doth a service to God.


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http://mileswmathis.com/vaxx2.pdf

Vaccine Approval for Children? No.

by Miles Mathis

First published November 10, 2021

Almost no one is noticing that the vaccine approved for children is Pfizer's Biontech vaccine, which IS
NOT fully approved for adults. So how can it be approved for children? Remember, the FDA
approved Pfizer's new Cominarty vaccine for adults, not the Biontech vaccine—and the Comirnaty
vaccine doesn't really exist. You will tell me the approval for children is just emergency use approval,
but that is illegal since the government is not allowed to approve an emergency use vaccine when a
normal use approval has been granted. If Cominarty is the same as Biontech, why not fully approve
Comirnaty for children, as it is for adults? It makes no sense. You will say it is because Comirnaty
hasn't hit the market yet, but if so that proves two things: there is no full approval of any existing
vaccine, and the whole announcement was nothing more than a fraud. Most people think the vaccine
for adults has full approval, but they have been conned. The vaccine they are getting is Biontech,
which does not have full approval and which has no legal backing. Pfizer is still exempt from all
lawsuits, with both children and adults.

Beyond that, we are now finding out the Pfizer vaccine for children is NEITHER Biontech nor
Comirnaty, since its list of ingredients is admitted to be different than either one by the CDC and FDA.
A vaccine is defined by its list of ingredients, and if that list changes it is no longer the same vaccine,
by definition. They have added an important new ingredient, that being an anti-heart-attack blood
thinner Tromethamine, to combat blood clotting. So the vaccine for children is even more dangerous
than the vaccine adults have been taking, with an extra poison in it. If your children get the vaccine,
they will be shot up not only with dangerous and untested mRNA technology spike proteins and
graphene adjuvants, they will at the same time be shot up with heart-attack drugs originally created for
old people and untested on five year olds. Five year olds don't normally get heart attacks, do they, so
there would be no reason to have previously tested Tromethamine on them.

Another problem just being noticed is that the vaccine and Tromethamine are meant to be given in
different ways, with one being indicated for introduction into muscle and one being indicated for
introduction into a vein. If you introduce the vaccine into a vein you can cause problems, and if you
don't introduce Tromethamine into a vein, you can cause problems. So they appear to be mixing drugs
with counter-indications, in some wild attempt to cover their ass on blood-clotting, and they are using
our children as guinea pigs for this insanity.

But what do they care: they aren't liable for any of this. Every child in America could die a horrible
death and they would still make billions scot-free. They have already murdered tens of thousands of
people and aren't being hunted with pitchforks, so they figure the sky is the limit on murdering for
profit these days.

And while the head of Pfizer is calling people who question his vaccines criminals, many countries in
the world are banning it or pausing it, due to the extreme harm being done. Mainstream outlets have
admitted major problems with the Pfizer vaccine from the beginning, including this msn.com article
from February and this Daily Mail article from March. That last one admits Pfizer has been linked to
more blood clots than AstraZenena, though AstraZeneca has been banned or paused in many more
first-world countries. Why? We may assume bigger payoffs or arm-twisting. Officials in Italy are
quoted admitting it is political, which means it is based on corporate pressure, of course, which is
normally wielded through money. The Daily Mail article itself is an example of this, since it goes on to
claim that no vaccine has any unusual risk level, and that there is no link between the vaccines and the
clots. What? They seem to be saying A and not-A in the same article, which is again indication of
multiple writers and corporate arm-twisting. But Pfizer itself is now admitting blood-clotting is a
problem by adding this blood thinner to the new vaccine. If blood-clotting is not caused by the
vaccine, why combine it with a blood thinner?

This is also informative: Pfizer not only required a liability waiver from countries like Argentina and
Brazil, it required collateral and guarantee funds, with assets like banks and military bases being put up
as seizable assets. So if you wondered why things went south with Bolsonaro, now you know. He was
targeted by Pfizer for not following orders. The entire Western Hemisphere is now just a puppet and
banana republic of Pfizer.

So this is just one more crime in a chain of outrageous crimes against humanity. You may say anyone
stupid enough to accept one of these vaccines deserves what he gets, but that isn't the case with
children, who aren't making their own decisions here. They are absolute victims, both of this crime
against humanity and of the ignorance and gullibility and misplaced trust of their parents.

[Dachsie]

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

What Will They Throw at Us Next? - Walking and Talking with Matt

13:04 video runtime

First published at 15:24 UTC on November 15th, 2021.

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XANDREWX

One of the United States Minor Outlying Islands

14071 subscribers

.
Category Education
Sensitivity Normal - Content that is suitable for ages 16 and over



1.
There will be intensified propaganda and threats against unvaccinated people.

2.
Many people will get sick this winter and unfortunately many will die.

3.
Now that the lockdowns have been firmly established in the people's minds, governments will begin to implement climate lockdowns.

4.
Inflation will go even higher.

5.
There will be significant supply-line disruptions and this will cause a lot of panic in the general population.

6.
There will be internet outages, rolling power blackouts, and other utilities disruptions.

7.
There will be fake bio-terror attacks that will scare people and require even tighter lockdowns and restricted travel.

[Dachsie]

https://www.trunews.com/stream/grave...ine-killed-him

1:21:30 video runtime

Grave Warning: Dead Man Says Covid-19 Vaccine Killed Him


Content Contributed By — TruNews Team

Take the broadcast was quite a bit on the subject of the PLANdemic;

Other news covered that Alex Jones Infowars was convicted in the defamation lawsuit against him. Dollar amount of daamges has n9t been announced yet. Alex Jones, as I understand it, has always refused full access to his personal financial as well as to Infowars.com and whatever the official corporation name is for Infowars.

Rick Wiles speaks against the Clay Clark "rallies types of events that are a combination of "Christian Zionism" and speech against the "virus" and the "vaccines" and pro-Trumpism and the kind of patriotism that perhaps best described as the ugly kind of nationalism.