Adolescents 12 to 15 years old need protection from FDA not Covid-19, News release contains lies, Lie 1: “potential benefits of this vaccine in individuals 12 years of age and older outweigh the known and potential risks”

Adolescents 12 to 15 years old need protection from FDA not Covid-19, News release contains lies, Lie 1: “potential benefits of this vaccine in individuals 12 years of age and older outweigh the known and potential risks”

“Why are we vaccinating healthy adults when 81 percent of Covid-19 cases are mild and there is  a 99 percent survival rate. Why are we testing vaccines on children who are minimally impacted by the disease?”…Citizen Wells

“it is my sincere hope that this public letter might stimulate FDA, Pfizer and Moderna leaders to think critically and quickly about the immunological danger the COVID-19 vaccine might pose to those persons naturally infected by SARS-CoV-2 — most especially to those infected who are recently convalescent, asymptomatic carriers, the elderly and frail or those with significant cardiovascular risk factors.”...Dr. Hooman Noorchashm

“VAERS received 4,434 reports of death (0.0017%) among people who received a COVID-19 vaccine.”...CDC May 11, 2021

From the FDA May 10, 2021.

“Coronavirus (COVID-19) Update: FDA Authorizes Pfizer-BioNTech COVID-19 Vaccine for Emergency Use in Adolescents in Another Important Action in Fight Against Pandemic

Today, the U.S. Food and Drug Administration expanded the emergency use authorization (EUA) for the Pfizer-BioNTech COVID-19 Vaccine for the prevention of coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) to include adolescents 12 through 15 years of age. The FDA amended the EUA originally issued on Dec. 11, 2020 for administration in individuals 16 years of age and older.

“The FDA’s expansion of the emergency use authorization for the Pfizer-BioNTech COVID-19 Vaccine to include adolescents 12 through 15 years of age is a significant step in the fight against the COVID-19 pandemic,” said Acting FDA Commissioner Janet Woodcock, M.D. “Today’s action allows for a younger population to be protected from COVID-19, bringing us closer to returning to a sense of normalcy and to ending the pandemic. Parents and guardians can rest assured that the agency undertook a rigorous and thorough review of all available data, as we have with all of our COVID-19 vaccine emergency use authorizations.”

From March 1, 2020 through April 30, 2021, approximately 1.5 million COVID-19 cases in individuals 11 to 17 years of age have been reported to the Centers for Disease Control and Prevention (CDC). Children and adolescents generally have a milder COVID-19 disease course as compared to adults. The Pfizer-BioNTech COVID-19 Vaccine is administered as a series of two doses, three weeks apart, the same dosage and dosing regimen for 16 years of age and older.

The FDA has determined that Pfizer-BioNTech COVID-19 Vaccine has met the statutory criteria to amend the EUA, and that the known and potential benefits of this vaccine in individuals 12 years of age and older outweigh the known and potential risks, supporting the vaccine’s use in this population. 

“Having a vaccine authorized for a younger population is a critical step in continuing to lessen the immense public health burden caused by the COVID-19 pandemic,” said Peter Marks, M.D., Ph.D., director of the FDA’s Center for Biologics Evaluation and Research. “With science guiding our evaluation and decision-making process, the FDA can assure the public and medical community that the available data meet our rigorous standards to support the emergency use of this vaccine in the adolescent population 12 years of age and older.”

The FDA has updated the Fact Sheets for Healthcare Providers Administering the Vaccine (Vaccination Providers) and for Recipients and Caregivers with information to reflect the use of the vaccine in the adolescent population, including the benefits and risks of the Pfizer-BioNTech COVID-19 Vaccine.

The EUA amendment for the Pfizer-BioNTech COVID-19 Vaccine was issued to Pfizer Inc. The issuance of an EUA is not an FDA approval (licensure) of a vaccine. The EUA will be effective until the declaration that circumstances exist justifying the authorization of the emergency use of drugs and biologics for prevention and treatment of COVID-19 is terminated, and may be revised or revoked if it is determined the EUA no longer meets the statutory criteria for issuance or to protect public health or safety.

FDA Evaluation of Available Safety Data

The available safety data to support the EUA in adolescents down to 12 years of age, include 2,260 participants ages 12 through 15 years old enrolled in an ongoing randomized, placebo-controlled clinical trial in the United States. Of these, 1,131 adolescent participants received the vaccine and 1,129 received a saline placebo. More than half of the participants were followed for safety for at least two months following the second dose.

The most commonly reported side effects in the adolescent clinical trial participants, which typically lasted 1-3 days, were pain at the injection site, tiredness, headache, chills, muscle pain, fever and joint pain. With the exception of pain at the injection site, more adolescents reported these side effects after the second dose than after the first dose, so it is important for vaccination providers and recipients to expect that there may be some side effects after either dose, but even more so after the second dose. The side effects in adolescents were consistent with those reported in clinical trial participants 16 years of age and older. It is important to note that as a general matter, while some individuals experience side effects following any vaccination, not every individual’s experience will be the same and some people may not experience side effects.

The Pfizer-BioNTech COVID-19 Vaccine should not be given to anyone with a known history of a severe allergic reaction, including anaphylaxis—to any component of the vaccine. Since its authorization for emergency use, rare severe allergic reactions, including anaphylaxis, have been reported following administration of the Pfizer-BioNTech COVID-19 Vaccine in some recipients.

FDA Evaluation of Available Effectiveness Data

The effectiveness data to support the EUA in adolescents down to 12 years of age is based on immunogenicity and an analysis of COVID-19 cases. The immune response to the vaccine in 190 participants, 12 through 15 years of age, was compared to the immune response of 170 participants, 16 through 25 years of age. In this analysis, the immune response of adolescents was non-inferior to (at least as good as) the immune response of the older participants. An analysis of cases of COVID-19 occurring among participants, 12 through 15 years of age, seven days after the second dose was also conducted. In this analysis, among participants without evidence of prior infection with SARS-CoV-2, no cases of COVID-19 occurred among 1,005 vaccine recipients and 16 cases of COVID-19 occurred among 978 placebo recipients; the vaccine was 100% effective in preventing COVID-19. At this time, there are limited data to address whether the vaccine can prevent transmission of the virus from person to person. In addition, at this time, data are not available to determine how long the vaccine will provide protection.

Ongoing Safety Monitoring

As part of the original EUA request, Pfizer Inc. submitted a plan to continue monitoring the safety of the vaccine as it is used under EUA. This plan has been updated to include the newly authorized adolescent population, and includes longer-term safety follow-up for participants enrolled in ongoing clinical trials, as well as other activities aimed at monitoring the safety of the Pfizer-BioNTech COVID-19 vaccine and ensuring that any safety concerns are identified and evaluated in a timely manner.

It is mandatory for Pfizer Inc. and vaccination providers to report the following to the Vaccine Adverse Event Reporting System for Pfizer-BioNTech COVID-19 Vaccine: all vaccine administration errors, serious adverse events, cases of Multisystem Inflammatory Syndrome and cases of COVID-19 that result in hospitalization or death.”

https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-authorizes-pfizer-biontech-covid-19-vaccine-emergency-use

Blatant lies.

Lie 1.

“potential benefits of this vaccine in individuals 12 years of age and older outweigh the known and potential risks”

Benefits?

CDC: “most children with COVID-19 have mild or no symptoms”

The FDA study states that 16 out of 978 placebo recipients got Covid. That is 1.6 percent.

The death rate for Covid in this age group is nearly statistically zero.

The known risks are frightening. The unknown perhaps more frightening. (see below)

Lie 2.

“An analysis of cases of COVID-19 occurring among participants, 12 through 15 years of age, seven days after the second dose was also conducted. In this analysis, among participants without evidence of prior infection with SARS-CoV-2, no cases of COVID-19 occurred among 1,005 vaccine recipients and 16 cases of COVID-19 occurred among 978 placebo recipients; the vaccine was 100% effective in preventing COVID-19.”

That does not prove that “the vaccine was 100% effective in preventing COVID-19.”

There is no way to prove that.

And furthermore, only 1.6 percent of placebo recipients getting Covid proves the vaccine is unnecessary.

Misleading statements.

Generally speaking, most of the news release is misleading.

Perhaps the worst offender in this category is the following.

“Parents and guardians can rest assured that the agency undertook a rigorous and thorough review of all available data, as we have with all of our COVID-19 vaccine emergency use authorizations.”

If they had reviewed all of the data the news release should not have happened.

Consider the following:

Just this week a 17 year old was hospitalized with 3 brain blood clots.

This is not an isolated incident.

CDC reports 4434 deaths “among people who received a COVID-19 vaccine”, Insufficient Informed Consent, Why FDA should not authorize vaccines for children

Adolescents 12 to 15 years old need protection from FDA not Covid-19

More here:

https://citizenwells.com/

http://citizenwells.net/

https://parler.com/profile/Citizenwells/posts

Covid vaccine deaths: “We’ve Seen More Deaths From This Shot Than All Vaccines in the Last 20 Years Combined”, Dr. Cole: “Never in the history of humanity have we quarantined the well,”

Covid vaccine deaths: “We’ve Seen More Deaths From This Shot Than All Vaccines in the Last 20 Years Combined”, Dr. Cole: “Never in the history of humanity have we quarantined the well,”

“Why are we vaccinating healthy adults when 81 percent of Covid-19 cases are mild and there is  a 99 percent survival rate. Why are we testing vaccines on children who are minimally impacted by the disease?”…Citizen Wells

“it is my sincere hope that this public letter might stimulate FDA, Pfizer and Moderna leaders to think critically and quickly about the immunological danger the COVID-19 vaccine might pose to those persons naturally infected by SARS-CoV-2 — most especially to those infected who are recently convalescent, asymptomatic carriers, the elderly and frail or those with significant cardiovascular risk factors.”...Dr. Hooman Noorchashm

“VAERS received 4,434 reports of death (0.0017%) among people who received a COVID-19 vaccine.”...CDC May 11, 2021

From GateWay Pundit May 12, 2021.

“Dr. Cole on Covid Jabs: “We’ve Seen More Deaths From This Shot Than All Vaccines in the Last 20 Years Combined”

Dr. Ryan Cole, owner and operator of Cole Diagnostics, has been very outspoken against the Covid lockdowns/quarantine and has warned about the mRNA vaccine.

The Idaho doctor on Wednesday said he is not anti-vaccine but he warned against the experimental Covid jabs.

“We’ve seen more deaths from this shot than all vaccines in the last 20 years combined — and that’s just in the first 4 to 5 months,” he said during an appearance on Rose Unplugged 1320 WJAS.”

“The doctor also said that a vaccine for Coronaviruses have never been approved because they lead to hyperimmune reactions in the long run.

“Never in the history of humanity have we quarantined the well,” Dr. Cole said arguing that lockdowns don’t work to stop the spread of Covid.”

Read more:

https://www.thegatewaypundit.com/2021/05/dr-cole-covid-jabs-seen-deaths-shot-vaccines-last-20-years-combined-audio/

More here:

https://citizenwells.com/

http://citizenwells.net/

https://parler.com/profile/Citizenwells/posts

CDC reports 4434 deaths “among people who received a COVID-19 vaccine”, Insufficient Informed Consent, Why FDA should not authorize vaccines for children

CDC reports 4434 deaths “among people who received a COVID-19 vaccine”, Insufficient Informed Consent, Why FDA should not authorize vaccines for children

“Why are we vaccinating healthy adults when 81 percent of Covid-19 cases are mild and there is  a 99 percent survival rate. Why are we testing vaccines on children who are minimally impacted by the disease?”…Citizen Wells

“it is my sincere hope that this public letter might stimulate FDA, Pfizer and Moderna leaders to think critically and quickly about the immunological danger the COVID-19 vaccine might pose to those persons naturally infected by SARS-CoV-2 — most especially to those infected who are recently convalescent, asymptomatic carriers, the elderly and frail or those with significant cardiovascular risk factors.”...Dr. Hooman Noorchashm

“VAERS received 4,434 reports of death (0.0017%) among people who received a COVID-19 vaccine.”...CDC May 11, 2021

From the CDC May 11, 2021.

“Over 259 million doses of COVID-19 vaccines were administered in the United States from December 14, 2020, through May 10, 2021. During this time, VAERS received 4,434 reports of death (0.0017%) among people who received a COVID-19 vaccine.”

https://www.cdc.gov/coronavirus/2019-ncov/vaccines/safety/adverse-events.html

Patients are not being properly informed to make a decision weighing the costs and benefits of receiving the vaccine.

Informed Consent legal definition:

“Consent of a patient or other recipient of services based on the principles
of autonomy and privacy; this has become the requirement at the center of
morally valid decision making in health care and research. Seven criteria
define informed consent: (1) competence to understand and to decide,
(2) voluntary decision making, (3) disclosure of material information,
(4) recommendation of a plan, (5) comprehension of terms (3) and (4),
(6) decision in favor of a plan, and (7) authorization of the plan.
A person gives informed consent only if all of these criteria are met.
If all of the criteria are met except that the person rejects the plan,
that person makes an informed refusal.”

From the CDC.

“For each COVID-19 vaccine authorized under an Emergency Use
Authorization (EUA),the Food and Drug Administration (FDA)
requires that vaccine recipients or their caregivers are
provided with certain vaccine-specific EUA information to
help make an informed decision about vaccination. This is
accomplished by providing an EUA Fact Sheet for Recipients
and Caregivers.”

Patients are not being informed, warned of the deaths that have occurred and serious injuries after vaccinations.

Therefore, minimally, all vaccinations should be halted until this is fixed and more information is available.

From The Defender May 11, 2021.

“Why FDA Should Not Authorize COVID Vaccines for Kids, Teens

The authors (two physicians and a professor) argue that Emergency Use Authorization for mass child vaccination presents a different balance of risks and benefits than it did for adults.”

“Pfizer has requested the FDA amend the existing EUA for its vaccine to allow eligibility for children aged 12 to 15, and further clinical trials of COVID-19 vaccines, including for younger children, are underway. Unlike for adults, however, the likelihood of severe outcomes or death associated with COVID-19 infection is very low for children, undermining the appropriateness of an EUA for child COVID-19 vaccines.”

Read more:

https://childrenshealthdefense.org/defender/why-fda-should-not-authorize-covid-vaccines-kids-teens/

More here:

https://citizenwells.com/

http://citizenwells.net/

https://parler.com/profile/Citizenwells/posts

17 year old male gets 3 brain blood clots after Pfizer Covid vaccine mother regrets decision, 1043 reports of blood clotting disorders attributed to Pfizer, No Informed Consent!

17 year old male gets 3 brain blood clots after Pfizer Covid vaccine mother regrets decision, 1043 reports of blood clotting disorders attributed to Pfizer, No Informed Consent!

“Why are we vaccinating healthy adults when 81 percent of Covid-19 cases are mild and there is  a 99 percent survival rate. Why are we testing vaccines on children who are minimally impacted by the disease?”…Citizen Wells

“VAERS received 4,178 reports of death (0.0017%) among people who received a COVID-19 vaccine.”...CDC May 5, 2021

“Patients are not being informed, warned of the deaths that have occurred and serious injuries after vaccinations.”…Citizen Wells

From The Defender May 10, 2021.

“Teen Hospitalized With Blood Clots in Brain After First Dose of Pfizer Vaccine

The mother of the 17-year-old, whose symptoms were initially dismissed as a pulled neck muscle, said she regrets her decision to allow him to be vaccinated.

A Utah teen remains hospitalized with three blood clots in and near his brain that developed after he received the first dose of Pfizer’s COVID vaccine.

Everest Romney, 17, received the vaccine April 21 and began experiencing neck pain, fever and severe headaches one day later. His mother, Cherie Romney, said her son’s pediatrician initially dismissed the symptoms as a pulled neck muscle. However, she was convinced it was something else, ABC4 News reported.

After more than a week of symptoms and being unable to freely move his neck, the family got this diagnosis: two blood clots inside his brain, and one on the outside.

“In a million years, I never expected it,” Romney said. “The worst thing, the worst thing, is to have the doctor come in and say, ‘OK, well, we found two blood clots inside his brain.’ The hardest thing was I let him get that shot. And he was healthy and well before. But you question it, you can’t help but question it when it all goes wrong.””

““In weighing the risk and benefits with COVID as opposed to COVID vaccinations, we strongly encourage our patients to become vaccinated because the risk is much less than the risk of the disease,” said University of Utah Health’s Dr. Richard Orlandi in a press conference.”

“After administering nearly 100 million doses of Pfizer’s vaccine, the CDC reported there hasn’t been a single related case of a blood clot forming in the brain as of April 12.

The CDC’s statement contradicts numerous news reportsstudiesscientists and the agency’s own system for monitoring adverse reactions, the Vaccine Adverse Event Reporting System (VAERS).

Utilizing a search criteria that included reports of blood clots associated with blood clotting disorders, VAERS yielded a total of 2,808 reports for all three vaccines from Dec. 14, 2020, through April 30. Of the 2,808 cases reported, there were 1,043 reports of blood clotting disorders attributed to Pfizer.

As The Defender reported in April, scientists warned U.S regulatory officials as far back as December 2020 that Pfizer and Moderna COVID vaccines pose similar blood clot risks as the Johnson & Johnson.”

Read more:

https://childrenshealthdefense.org/defender/teen-hospitalized-brain-blood-clots-after-pfizer-vaccine/

Why are we vaccinating children who are at little risk from Covid and known and unknown risks from the vaccines?

More here:

https://citizenwells.com/

http://citizenwells.net/

https://parler.com/profile/Citizenwells/posts

President Trump statement on Michigan election lawsuit Bailey v Antrim County May 10, 2021, “Michigan Election Fraud case has just filed a bombshell pleading claiming votes were intentionally switched”

President Trump statement on Michigan election lawsuit Bailey v Antrim County May 10, 2021, “Michigan Election Fraud case has just filed a bombshell pleading claiming votes were intentionally switched”

“practice of assigning names and numbers” to non-eligible voters who did not appear in either the poll book or the supplement poll book. “…Poll worker Zachary Larsen, former MI Asst. AG

“The only reason to change software after the election would be to obfuscate
evidence of fraud and/or to correct program errors that would de-certify the
election. Our findings show that the Central Lake Township tabulator tape totals
were significantly altered by utilizing two different program versions (10/23/2020 and 11/05/2020), both of which were software changes during an election which violates election law, and not just human error associated with the Dominion Election Management System. This is clear evidence of software generated movement of votes. The claims made on the Office of the Secretary of State website are false.”…Antrim County audit report

“Trump’s not gonna win. I made f*cking sure of that!”...Eric Coomer, executive with Dominion Voting Systems

From President Donald Trump May 10, 2021.

“The major Michigan Election Fraud case has just filed a bombshell pleading claiming votes were intentionally switched from President Trump to Joe Biden. The number of votes is MASSIVE and determinative. This will prove true in numerous other States. All Republicans must UNIFY and not let this happen. If a thief robs a jewelry store of all of its diamonds (the 2020 Presidential Election), the diamonds must be returned. The Fake News media refuses to cover the greatest Election Fraud in the history of our Country. They have lost all credibility, but ultimately, they will have no choice!”

 https://www.donaldjtrump.com/news/statement-by-donald-j-trump-45th-president-of-the-united-states-of-america-05.10.21-4

Antrim County Hearing May 10, 2021.

From Citizen Wells May 8, 2021.

From Attorney Matthew DePerno in

Bailey v Antrim County MI (Jocelyn Benson) 


Matthew S. DePerno, Esq.@mdeperno

New discoveries and filings today: (1) 1,061 phantom ballots discovered in Antrim

(2) nearly 100% turnout between ages 65 and 80

(3) 20.3% of all ballots sent to PO boxes

From

Plaintiff’s Response to Joint Motion for Summary Disposition

Filed May 3, 2021.

“Guy and Benson worked in unison with Election Source to rig the election
by manipulating the Dominion Voting System and altering data to transfer
votes from Donald Trump to Joseph Biden.”

“Indeed, the United States Supreme Court ruled….that “fraud vitiates everything.””

More here:

https://citizenwells.com/

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Arizona Dominion Voting Systems passwords: why is AZ just now requesting admin passwords?, Why was Dominion given control?, Katie Hobbs complicit?, Nov 30 election witness Jan Bryant revealed

Arizona Dominion Voting Systems passwords: why is AZ just now requesting admin passwords?, Why was Dominion given control?, Katie Hobbs complicit?, Nov 30 election witness Jan Bryant revealed

“Trump’s not gonna win. I made f*cking sure of that!”...Eric Coomer, executive with Dominion Voting Systems

“The certification of Arizona’s FALSE results is unethical and knowingly participating in the corruption that has disenfranchised AZ voters,” …Jenna Ellis

“.@realDonaldTrump has made it abundantly clear he’s more interested in pandering to his neo-nazi base than being @POTUS for all Americans.”…Katie Hobbs Arizona Secretary of State

During the November election hearing in Arizona, witness Jan Bryant revealed that Dominion Voting Systems employees controlled the election.

Why was Dominion given control of the 2020 Arizona election processing?

Why was Dominion given control of the 2 % hand audit?

Was AZ Secretary of State Katie Hobbs complicit?

Why is Arizona just now requesting admin passwords?

Why is Dominion not complying with subpoenas?

From TeaParty.org.

“AZ Audit Director Says Dominion Refusing To Comply With Subpoena And Won’t Turn Over Password To Their Machines

There are many forces trying to stop the 2020 election audit going on in Maricopa County, Arizona.

The Democrats have sent a mob of lawyers to the state in an effort to find any infraction of the law they can, the Secretary of State of the Maricopa County Board of Supervisors have been interfering and impeding the efforts from the beginning and now Dominion is doing their part.

During an interview with One America News Network, Arizona audit director Ken Bennett claimed that the Maricopa County Election Board (MECB) does not have an “admin” password needed to access the administrative functions of the election machines.

This is alarming news. That means that the Maricopa County Election Board did not have control over the election and that Dominion had more access than they did.

According to The Gateway Pundit, the MCEB ceded control of the election to Dominion. The system administrators are people who have access to the systems at their highest levels. It’s clear that the system administrators were not the MCEB but rather the corrupt Dominion.

That means that employees of Dominion were able to perform all the functions of the system and make changes in the system like deleting or altering system logs. Dominion, rather than elected county officials, had complete and total control over the 2020 election in the county.”

Read more:

https://www.teaparty.org/breaking-az-audit-director-says-dominion-refusing-to-comply-with-subpoena-and-wont-turn-over-password-to-their-machines-464482/

From GateWay Pundit.

“Maricopa County Elections Witness Testifies that Dominion Ran Entire Election – County Officials and Observers NEVER HAD Access or Passwords!

Back on November 30, 2020, Maricopa County elections witness Jan Bryant testified before the Arizona legislature.

Jan said back on November 30, 2020, that Maricopa County officials DID NOT RUN THE ELECTION!  Dominion employees John and Bruce did.

“I also participated in the (2%) random ballot selection for hand audit. Picking the ballots, you know, determining which bins we were going to select. And even with that, Dominion ran the report for it (which bins to pull). So no one, I mean, they (Dominion) knew exactly what was in the hand audit boxes. That made me nervous also. And they also knew when we pulled the last box, which was probably eight days before they quit counting ballots. As a senior manager over big projects, never in a million years would I have allowed some of the stuff that I saw going on there.

RECAP: The exact bins to be pulled for the mandated 2% hand audit were decided by Dominion staff, using their EMS software, not randomly.

Read more:

https://www.thegatewaypundit.com/2021/05/maricopa-county-elections-witness-testifies-dominion-ran-entire-election-county-officials-observers-never-access-passwords-video/

More here:

https://citizenwells.com/

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https://parler.com/profile/Citizenwells/posts

Seth Rich records release FBI given until July 24, 2021, Over 5 years since Rich was murdered, Huddleston v FBI, “Given _________, it is conceivable that an individual or group would want to pay for his death.”

Seth Rich records release FBI given until July 24, 2021, Over 5 years since Rich was murdered, Huddleston v FBI, “Given _________, it is conceivable that an individual or group would want to pay for his death.”

“And why is Fox News working so hard to kill this story? I wish I could say more “about Fox’s behind-the-scenes treachery — and someday hopefully I will — but rest assured that Malia Zimmerman’s May 17, 2017 story about Mr. Rich was fully vetted by senior Fox management. I repeatedly encouraged Fox’s attorneys to postpone settlement discussions with Seth Rich’s parents until I obtained the FBI records (my client, Ed Butowsky, was a co-defendant with Fox), but Fox was hellbent on settling the case in October / November. That’s around the time Rupert Murdoch publicly joined forces with Joe Biden. Fox had a very strong defense, yet it rolled over and played dead, settling the lawsuit and then firing Ms. Zimmerman. Sooner or later, the full story will come out, and it will be very ugly for Fox News and the Murdoch family.”...Attorney Ty Clevenger

“They found, what he had done, he [Seth Rich] had submitted a series of documents, emails from DNC — and, by the way, all this shit about the DNC, you know, was it a ‘hack’ or wasn’t it a ‘hack’ — whatever happened, it was the Democrats themselves wrote this shit, you know what I mean? All I know is that, he offered a sample, he sends a sample, you know, I am sure dozens of emails, and said ‘I want money’. Later Wikileaks did get the password [SETH RICH DID SELL WIKILEAKS ACCESS INTO HIS COMPUTER.] He had a drop-box, a [password-]protected drop-box, which isn’t hard to do.”…Seymour Hersh

” So why would a “street robbery” investigation need to be classified?”…Attorney Ty Clevenger July 22, 2020

From Huddleston v FBI May 7, 2021.

“MEMORANDUM OPINION AND ORDER. It is therefore ORDERED that Defendants’ Second Motion to Stay Scheduling Order Deadlines (Dkt. [21]) is hereby GRANTED. It is FURTHER ORDERED that the Scheduling Order in this case is amended as follows: April 23, 2021 First Production, May 24, 2021 Second Production, June 24, 2021 Third Production, July 24, 2021 Final Production. Signed by District Judge Amos L. Mazzant, III on 5/7/2021. (filed: 05/07/2021)”

https://www.docketbird.com/court-cases/Huddleston-v-Federal-Bureau-of-Investigation/txed-4:2020-cv-00447

The FBI has been given until July 24, 2021 to produce all records related to Seth Rich.

That will be over 5 years after his murder.

From Citizen Wells April 24, 2021.

From Attorney Ty Clevenger April 23, 2021.

“This afternoon the FBI finally released records about murdered DNC employee Seth Rich and the 2016 theft of Democratic National Committee emails that were later published by Wikileaks. Those documents provide new information, but generally raise more questions than answers.

Of 576 relevant pages identified by the FBI, only 68 were produced, and most of those 68 pages are heavily redacted. They reference Roger Stone, Paul Manafort, Richard Gates, Donald Trump, Jr., Jay Sekulow, and Jerome Corsi, among others.

I haven’t had time to thoroughly review the documents, but here are a few things that stand out:

  • On page 64, a November 11, 2017 memo from FBI’s Boston Field Office is almost completely redacted, but the last sentence reads as follows: “Given _________, it is conceivable that an individual or group would want to pay for his death.”
  • A witness interview form begins on page 65, and it appears to be the interview of former Asst. U.S. Attorney Deborah Sines, the prosecutor assigned to the Seth Rich murder case. [Continued on p.2]

Page 66 of that interview reads as follows: ““After the homicide, ____ took Rich’s personal laptop to his house in ____. ____ was not aware of if _____ deleted or changed anything on Rich’s laptop.” I suspect this is referring to Aaron Rich, brother of Seth, and it begs a question: why would a private citizen be allowed to carry away evidence relevant to a murder investigation? Why was this not immediately given to the police rather than taken to somebody’s house? And the government is not aware of whether this private citizen deleted anything from the laptop? That seems like an important thing to figure out.”

“I reported last December that the NSA was withholding records about Seth Rich, and my inside source tells me it’s more than 32 pages. Regardless of the number of pages, I think we can piece together what happened. Thanks to Edward Snowden, we know that the NSA intercepts and stores virtually every electronic communication in or out of the United States. The agency is supposed to store all of that information without looking at it, and the data is supposed to be mined only upon request from an authorized entity.

I suspect Robert Mueller’s staff asked the NSA to mine the data for communications between Seth Rich (possibly Aaron Rich) and Wikileaks, and I suspect the NSA provided 32 pages of responsive records to Mueller. Now both agencies want to hide the contents of those 32 pages. Why?

If you’re discouraged by all of the redactions and withheld pages, don’t be. I plan to ask U.S. District Judge Amos Mazzant to review unredacted copies of all of these documents to determine whether information is improperly being withheld. Judge Mazzant is a straight shooter, and I suspect he will grant my request.”

More here:

https://citizenwells.com/

http://citizenwells.net/

https://parler.com/profile/Citizenwells/posts

Bailey v Antrim County MI update May 8, 2021 “New discoveries and filings”, 1061 phantom ballots discovered in Antrim, “fraud vitiates everything”

Bailey v Antrim County MI update May 8, 2021 “New discoveries and filings”, 1061 phantom ballots discovered in Antrim, “fraud vitiates everything”

“practice of assigning names and numbers” to non-eligible voters who did not appear in either the poll book or the supplement poll book. “…Poll worker Zachary Larsen, former MI Asst. AG

“The only reason to change software after the election would be to obfuscate
evidence of fraud and/or to correct program errors that would de-certify the
election. Our findings show that the Central Lake Township tabulator tape totals
were significantly altered by utilizing two different program versions (10/23/2020 and 11/05/2020), both of which were software changes during an election which violates election law, and not just human error associated with the Dominion Election Management System. This is clear evidence of software generated movement of votes. The claims made on the Office of the Secretary of State website are false.”…Antrim County audit report

“Trump’s not gonna win. I made f*cking sure of that!”...Eric Coomer, executive with Dominion Voting Systems

From Attorney Matthew DePerno in

Bailey v Antrim County MI (Jocelyn Benson) 


Matthew S. DePerno, Esq.@mdeperno

New discoveries and filings today: (1) 1,061 phantom ballots discovered in Antrim

(2) nearly 100% turnout between ages 65 and 80

(3) 20.3% of all ballots sent to PO boxes

From

Plaintiff’s Response to Joint Motion for Summary Disposition

Filed May 3, 2021.

“Guy and Benson worked in unison with Election Source to rig the election
by manipulating the Dominion Voting System and altering data to transfer
votes from Donald Trump to Joseph Biden.”

“Indeed, the United States Supreme Court ruled….that “fraud vitiates everything.”

https://www.depernolaw.com/bailey-documents—may-2021.html

Citizen Wells May 5, 2021.

Antrim County Michigan audit proves Dominion Voting Machines capable of flipping votes, Attorney Matthew DePerno interview on Mike Lindell’s FrankSpeech.com, Four Shocking Discoveries

More here:

https://citizenwells.com/

http://citizenwells.net/

https://parler.com/profile/Citizenwells/posts

Covid-19 vaccines Informed Consent Disclosures not warning patients of death and serious injury risks, Part 1, All vaccinations should be halted

Covid-19 vaccines Informed Consent Disclosures not warning patients of death and serious injury risks, Part 1, All vaccinations should be halted

“Why are we vaccinating healthy adults when 81 percent of Covid-19 cases are mild and there is  a 99 percent survival rate. Why are we testing vaccines on children who are minimally impacted by the disease?”…Citizen Wells

“it is my sincere hope that this public letter might stimulate FDA, Pfizer and Moderna leaders to think critically and quickly about the immunological danger the COVID-19 vaccine might pose to those persons naturally infected by SARS-CoV-2 — most especially to those infected who are recently convalescent, asymptomatic carriers, the elderly and frail or those with significant cardiovascular risk factors.”...Dr. Hooman Noorchashm

“VAERS received 4,178 reports of death (0.0017%) among people who received a COVID-19 vaccine.”...CDC May 5, 2021

Informed Consent legal definition:

“Consent of a patient or other recipient of services based on the principles
of autonomy and privacy; this has become the requirement at the center of
morally valid decision making in health care and research. Seven criteria
define informed consent: (1) competence to understand and to decide,
(2) voluntary decision making, (3) disclosure of material information,
(4) recommendation of a plan, (5) comprehension of terms (3) and (4),
(6) decision in favor of a plan, and (7) authorization of the plan.
A person gives informed consent only if all of these criteria are met.
If all of the criteria are met except that the person rejects the plan,
that person makes an informed refusal.”

From the CDC.

“For each COVID-19 vaccine authorized under an Emergency Use
Authorization (EUA),the Food and Drug Administration (FDA)
requires that vaccine recipients or their caregivers are
provided with certain vaccine-specific EUA information to
help make an informed decision about vaccination. This is
accomplished by providing an EUA Fact Sheet for Recipients
and Caregivers.”

https://www.cdc.gov/vaccines/covid-19/eua/index.html

Pfizer EUA.

“WHAT ARE THE RISKS OF THE PFIZER-BIONTECH COVID-19 VACCINE?
There is a remote chance that the Pfizer-BioNTech COVID-19 Vaccine could cause a
severe allergic reaction. A severe allergic reaction would usually occur within a few
minutes to one hour after getting a dose of the Pfizer-BioNTech COVID-19 Vaccine. For
this reason, your vaccination provider may ask you to stay at the place where you
received your vaccine for monitoring after vaccination. Signs of a severe allergic
reaction can include:
• Difficulty breathing
• Swelling of your face and throat
• A fast heartbeat
• A bad rash all over your body
• Dizziness and weakness
Side effects that have been reported with the Pfizer-BioNTech COVID-19 Vaccine
include:
• severe allergic reactions
• non-severe allergic reactions such as rash, itching, hives, or swelling of the face
• injection site pain
• tiredness
• headache
• muscle pain
• chills
• joint pain
• fever
• injection site swelling
• injection site redness
• nausea
• feeling unwell
• swollen lymph nodes (lymphadenopathy)

• diarrhea
• vomiting
• arm pain

These may not be all the possible side effects of the Pfizer-BioNTech COVID-19
Vaccine. Serious and unexpected side effects may occur. Pfizer-BioNTech COVID-19
Vaccine is still being studied in clinical trials.”

https://www.fda.gov/media/144414/download

Moderna EUA.

“WHAT ARE THE RISKS OF THE MODERNA COVID-19 VACCINE?
There is a remote chance that the Moderna COVID-19 Vaccine could cause a severe allergic
reaction. A severe allergic reaction would usually occur within a few minutes to one hour after
getting a dose of the Moderna COVID-19 Vaccine. For this reason, your vaccination provider
may ask you to stay at the place where you received your vaccine for monitoring after
vaccination. Signs of a severe allergic reaction can include:
• Difficulty breathing
• Swelling of your face and throat
• A fast heartbeat
• A bad rash all over your body
• Dizziness and weakness
Side effects that have been reported in a clinical trial with the Moderna COVID-19 Vaccine
include:
• Injection site reactions: pain, tenderness and swelling of the lymph nodes in the same arm
of the injection, swelling (hardness), and redness
• General side effects: fatigue, headache, muscle pain, joint pain, chills, nausea and
vomiting, and fever
Side effects that have been reported during post-authorization use of the Moderna COVID-19
Vaccine include:
• Severe allergic reactions
These may not be all the possible side effects of the Moderna COVID-19 Vaccine. Serious and
unexpected side effects may occur. The Moderna COVID-19 Vaccine is still being studied in
clinical trials.”

Jannsen EUA.

“WHAT ARE THE RISKS OF THE JANSSEN COVID-19 VACCINE?
Side effects that have been reported with the Janssen COVID-19 Vaccine include:
• Injection site reactions: pain, redness of the skin and swelling.
• General side effects: headache, feeling very tired, muscle aches, nausea, and fever.
There is a remote chance that the Janssen COVID-19 Vaccine could cause a severe allergic
reaction. A severe allergic reaction would usually occur within a few minutes to one hour after
getting a dose of the Janssen COVID-19 Vaccine. For this reason, your vaccination provider may
ask you to stay at the place where you received your vaccine for monitoring after vaccination.
Signs of a severe allergic reaction can include:
• Difficulty breathing,
• Swelling of your face and throat,
• A fast heartbeat,
• A bad rash all over your body,
• Dizziness and weakness.
Blood clots involving blood vessels in the brain, abdomen, and legs along with low levels of
platelets (blood cells that help your body stop bleeding), have occurred in some people who have
received the Janssen COVID-19 Vaccine. In people who developed these blood clots and low levels
of platelets, symptoms began approximately one to two-weeks following vaccination. Most people
who developed these blood clots and low levels of platelets were females ages 18 through 49 years.
The chance of having this occur is remote. You should seek medical attention right away if you
have any of the following symptoms after receiving Janssen COVID-19 Vaccine:
• Shortness of breath,
• Chest pain,
• Leg swelling,
• Persistent abdominal pain,
• Severe or persistent headaches or blurred vision,
• Easy bruising or tiny blood spots under the skin beyond the site of the injection.

These may not be all the possible side effects of the Janssen COVID-19 Vaccine. Serious and
unexpected effects may occur. The Janssen COVID-19 Vaccine is still being studied in clinical
trials.”

No mention of deaths or very serious injuries that have occurred after the vaccinations.

From the NIH.

Aims of the study: Patient comprehension is a critical part of meeting medical ethics standards of informed consent in study designs. The aim of the study was to determine if sufficient literature exists to require clinicians to disclose the specific risk that COVID-19 vaccines could worsen disease upon exposure to challenge or circulating virus.”

Results of the study: COVID-19 vaccines designed to elicit neutralising antibodies may sensitise vaccine recipients to more severe disease than if they were not vaccinated. Vaccines for SARS, MERS and RSV have never been approved, and the data generated in the development and testing of these vaccines suggest a serious mechanistic concern: that vaccines designed empirically using the traditional approach (consisting of the unmodified or minimally modified coronavirus viral spike to elicit neutralising antibodies), be they composed of protein, viral vector, DNA or RNA and irrespective of delivery method, may worsen COVID-19 disease via antibody-dependent enhancement (ADE). This risk is sufficiently obscured in clinical trial protocols and consent forms for ongoing COVID-19 vaccine trials that adequate patient comprehension of this risk is unlikely to occur, obviating truly informed consent by subjects in these trials.

Conclusions drawn from the study and clinical implications: The specific and significant COVID-19 risk of ADE should have been and should be prominently and independently disclosed to research subjects currently in vaccine trials, as well as those being recruited for the trials and future patients after vaccine approval, in order to meet the medical ethics standard of patient comprehension for informed consent.”

https://pubmed.ncbi.nlm.nih.gov/33113270/

4178 deaths after Covid-19 vaccine reported by CDC, 1099 cases of Bell’s Palsy, 121 cases of Guillain Barre, 33673 Anaphylaxis, Dr. Peter McCullough sounds alarm

Patients are not being informed, warned of the deaths that have occurred and serious injuries after vaccinations.

Therefore, minimally, all vaccinations should be halted until this is fixed and more information is available.

More here:

https://citizenwells.com/

http://citizenwells.net/

https://parler.com/profile/Citizenwells/posts

Parler down for days what is going on?, @parler_app tweets tell little, May 5 update: “UPDATE 2: Team says it will be two more hours, so offline until about 11 am”???

Parler down for days what is going on?, @parler_app tweets tell little, May 5 update: “UPDATE 2: Team says it will be two more hours, so offline until about 11 am”???

“If you tell a lie big enough and keep repeating it, people will eventually come to believe it.”…Joseph Goebbels

“The Components of Hitler’s Propaganda Machine
To poison German attitudes toward Jews, the Nazis built a tremendous propaganda machine. But what were its components? Hitler and
his henchmen persuaded German citizens to destroy the Jews in three
principal ways: (1) through pervasive hate rhetoric from leading members of the Nazi power hierarchy; (2) through coordinating all hate
speech activity via creation of the Reich Ministry of Public Enlightenment and Propaganda (Propaganda Ministry), helmed by Joseph Goebbels; and (3) through eliminating independent print media.”...Nuremberg Propaganda Prosecutions

“For we wrestle not against flesh and blood, but against principalities, against powers, against the rulers of the darkness of this world, against spiritual wickedness in high places.”…Ephesians 6:12

Parler.com has been down for days.

What is going on?

The following message is displayed on their site:

“The team is hard at work, tidying up and bringing you some cool changes. Take a break – we’ll see you in a few hours.”

From Twitter:


Parler@parler_app·UPDATE 2: Team says it will be two more hours, so offline until about 11 am PT #parlerQuote Tweet

Parler@parler_app · May 5UPDATE: The tech team is saying we might be offline for up to 2 more hours, until 9 am PT #parler twitter.com/parler_app/sta…1073478Parler@parler_app·UPDATE: The tech team is saying we might be offline for up to 2 more hours, until 9 am PT #parlerQuote Tweet

Parler@parler_app · May 5Parler is currently inaccessible while we’re working on enhancements to the core system. In the long run, this will heighten the platform’s stability and user experience. We should be back online by 7 am PST. #parler #updates212168Parler@parler_app·Parler is currently inaccessible while we’re working on enhancements to the core system. In the long run, this will heighten the platform’s stability and user experience. We should be back online by 7 am PST. #parler#updates

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https://parler.com/profile/Citizenwells/posts