Good Bad, and the Ugly.
David Walter Banks/The Washington Post/Brandon Bell/Getty Images
Fulton County District Attorney Fani Willis speaks in the Fulton County Government Center during a news conference in Atlanta, Georgia, on Aug. 14. (John Bazemore / AP)
The chair of Georgia’s Freedom Caucus said that it is time the Fulton County district attorney who has spent more than two years working up to the indictment of former President Donald Trump faced legislative scrutiny.
Trump was indicted last week on conspiracy charges related to his challenge of the 2020 election.
Republican state Rep. Charlice Byrd announced on social media that she is supporting an effort from Republican state Sen. Colton Moore to investigate DA Fani Willis.
“I was elected to do a job, not sit on the sidelines. Given the concerning nature of the recent indictment in Fulton County, I have signed on to Senator Colton Moore’s letter calling for an emergency special session. I encourage my colleagues to do the same,” she posted on her Facebook page.
In a statement posted on social media, she wrote “Having reviewed the evidence of possible corruption in the Fulton County District Attorney’s Office, specifically regarding the indictment of President Donald Trump and eighteen others, I believe it is time the General Assembly investigated this matter.”
She said that she supports Moore’s call for “an emergency special session of the General Assembly to investigate possible malfeasance.”
“If wrongdoing is found, as a duly elected member of the Georgia House of Representatives I am prepared to begin the impeachment process,” she wrote.
“The people demand this matter be investigated fully,” she wrote, calling upon other members to support the proposal.
“We must seek the truth by doing our constitutional duty of overseeing the judicial system, to ensure the oath of office enshrined in law, that every District Attorney must take before assuming office, is respected and adhered to,” she continued.
Last week, when Trump’s indictment was announced, Byrd posted on Facebook, “It’s a dark day in Georgia but the Georgia Freedom Caucus and our coalition partners won’t sit by and watch this totalitarian corruption.”
“We must strip all funding and, if appropriate, impeach Fani Willis,” Moore said in a statement last week when he announced his call for a special session, according to Breitbart.
“As a Georgia State Senator, I am officially calling for an emergency session to review the actions of Fani Willis. America is under attack. I’m not going to sit back and watch as radical left prosecutors weaponize their elected offices to politically target their opponents,” he said.
The look of desperation.Joe Raedle / Getty
Trump will be arraigned on the charges against him on Thursday.
I guess these single-digit IQs think they can hold on to power forever. Otherwise, they’d be worried about what’s going to happen to them when the other side uses their tactics against them. — TPR
Damning Life Insurance Data PROVES Far More Young People Are Dying — And It’s NOT from COVID
When data speaks, we must listen.
Thanks to Vigilant Fox
When data speaks, we must listen. And statistics from the Society of Actuaries reveal a harrowing health crisis in the American youth. While most of the attention has been directed towards the COVID-19 pandemic and its consequences, there’s an underreported situation emerging — a rise in the mortality rate of younger individuals. Disturbingly, these figures can’t solely be attributed to COVID-19 — far from it.
According to the data reported by the Society of Actuaries, which conducts research for the insurance industry, there is a concerning trend in deaths among the young. Much of this data comes from the US Centers for Disease Control and Prevention (CDC), which has limitations with respect to data collection and transparency.
Actual-to-Expected (A/E) Death Ratios
To understand the gravity of the situation, retired nurse educator and respected medical figure Dr. John Campbell, walked through the Society of Actuaries data actual-to-expected (A/E) death ratios. The “actual” part of the ratio is the number of deaths that were actually recorded, and the “expected” part of the ratio refers to the number of deaths we would expect to see – using a 2015 to 2019 baseline.
Between April to December 2020, during the peak of the pandemic, the A/E ratio was 122%. This means there were 22% more deaths than expected. Excess mortality for all of 2020, including January to March, was recorded at 16.4%. 13.3% of the excess deaths were attributed to COVID, and 3.1% of the excess deaths were not. This makes sense because, at the time, there were no “miracle vaccines” to save us.
Fast forward to 2021, a year when vaccines were touted as our saving grace. The A/E ratio was at 117%, nearly mirroring 2020’s figures. Logic would suggest that with the rollout of vaccines, mortality rates, especially those related to COVID, should have declined. But they didn’t. And when it comes to non-COVID deaths, 15 to 34-year-olds saw a staggering 21.4% increasein excess deaths in 2021.
2022, primarily characterized by the less-severe Omicron variant, should have witnessed a sharp drop in excess mortality given the less virulent strain and increased vaccination rates. Instead, data up to March 2022 indicated an A/E ratio of 115% — and this figure excluded COVID deaths. Given this, one is compelled to infer that something went deeply wrong with pandemic measures. Most worrying, deaths among 35 to 44-year-olds, between October and December 2022, surged an alarming 34% above the expected 2015 to 2019 baseline.
Looking at graphical representations, particularly among males and females aged 15 to 34, the numbers stay consistently above the expected baselines. What’s more concerning is that these figures can’t solely be attributed to a lack of access to healthcare, as some pundits suggest. If this were the primary factor, the oldest age groups, more reliant on medical care, would see the highest excess deaths. Instead, it’s the younger and, often, healthier age ranges witnessing the most significant surges. The mainstream narrative is just not making sense.
Dowd’s book has thoroughly compiled headline after headline, of young people suddenly dying of an “unknown” cause. What you’re about to watch in the video below is young and healthy people, in the prime of their lives, suddenly and unexpectedly collapsing and dying. And this is just from the past eight months…
During the pandemic, we were told the measures were about “health” and “saving lives.” But in the midst of a major health crisis among young and working-aged people, health authorities are radio silent. Why is that? And why does no one seem to care what’s causing it? Because while COVID-19 is now well behind us, a more insidious health crisis is unfolding right before our eyes.
Well, it’s another day and we’re getting yet another explanation from Fulton Country officials when it comes to the posted-then-deleted document that appeared to be the indictment against former President Donald Trump — and it might be the wildest one yet.
As Townhall reported previously, a document that showed a number of charges under Trump’s name appeared on the Fulton County clerk’s website on Monday around noon, but was quickly removed. Later that night, when the grand jury voted on the indictment, it turned out that Trump was charged with exactly the same counts as had appeared on the clerk’s website hours before the grand jury had completed its work. County officials called the deleted document “fictitious” initially on Monday, then changed tact on Tuesday to say it was the result of a “trial run” used to “test” the system of posting indictments in anticipation of the grand jury’s vote.
At no time, however, amid the changing stories, have Fulton County officials explained why the document posted initially was an exact match for the charges the grand jury actually handed up hours later.
On Wednesday, we got another story — this time directly from Fulton County Clerk Ché Alexander — that added more information but did little to clear up the situation.
Here’s what she had to say when she broke her silence in an interview with Atlanta ABC affiliate WSB-TV:
She says she was under a lot of pressure to make sure the process went smoothly. In trying to be perfect she says she made a mistake.
She says she hit send instead of hitting save. “I am human,” she said. And she says she wanted to get the documents to the public as soon as possible.
“And that’s how the mishap happened.”
Alexander said this had nothing to do with the D.A.’s office and there was nothing sinister about the mistake she made.
“I have no dog in the fight,” she pointed out.
She says in an effort to handle the indictment perfectly, she messed up. “I did a work sample in the system. And when I hit save, it went to the press queue.”
Some news reporters saw it before it was deleted. At least one outlet published it.
Alexander says what was published was unofficial. “It wasn’t an official document. It wasn’t official charges. It was the dry run. It was a work sample,” she said.
Even though it had a case number. But Alexander says it didn’t have a stamp or other markings that would have made it official.
Jones asked her why did she release a statement calling the document “fictitious.”
“That was the best word that I could come up with. It was fictitious. It wasn’t real. It didn’t have a stamp on it,” she stated.
Jones asked her why she didn’t just say it was an error. Alexander says the word ‘fictitious’ is what her team came up with…
Alexander says she was under a lot of worldwide pressure to get this right. Now she says she just wants to explain what happened and get back to work. “I tell my staff we just want to be transparent. I don’t have anything to hide,” Alexander said.
Alexander says her mistake had no impact on the grand jury and its decision.
Yep, the latest version of events is that the clerk “hit send instead of save.” Notably, there’s still no explanation for how the test run which went awry happened to include the exact counts on which Trump was later indicted by the grand jury, but with any luck there will be yet another explanation or statement from the clerk’s office yet to be released in the days ahead.
Sorry, (Ms) Charley, but your “explanation” won’t wash. As the owner of several websites across different hosts, I can tell you that the “Save” and “Send” (or “Publish”) are NOT next to each other.
“under a lot of worldwide pressure to get this right.”
WORLDWIDE pressure???????? Who the @$#%$! does she think she’s fooling? Oh, right. Leftist drones accept anything — no matter how outrageous — as long as it comes from an approved source –TPR
YouTube is taking immediate action to expand its “medical misinformation” censorship policies, according to a blog post by the popular video platform on Tuesday.
YouTube is streamlining its existing policy to three distinct categories in anticipation of a more long-term suppression of medical information authorities disagree with, according to the announcement. A significant portion of YouTube’s announcement focuses on how it will now censor certain cancer-related content.
“Starting today and ramping up in the coming weeks, we will begin removing content that promotes cancer treatments proven to be harmful or ineffective, or content that discourages viewers from seeking professional medical treatment,” the announcement states.
YouTube acknowledges the evolving nature of medical knowledge and information in its announcement.
However, “our goal is to ensure that when it comes to areas of well-studied scientific consensus, YouTube is not a platform for distributing information that could harm people,” its announcement states.
The three categories of “medical misinformation” will be Prevention, Treatment and Denial, according to the announcement. They state that YouTube will remove content that “contradicts health authority guidance.”
Democratic presidential candidate Robert F. Kennedy Jr. is suing YouTube and its parent company, Google, for allegedly violating his free speech, according to a complaint filed Aug. 2. YouTube has removed Kennedy’s videos because of its “vaccine misinformation” policies on multiple occasions, according to the complaint.
Since “YouTube does not allow people to say anything ‘that contradicts local health authorities’ (LHA) or the World Health Organization’s (WHO) medical information about COVID-19,’” this means the government sets the medical censorship guidelines, Kennedy’s lawsuit alleges.
(Washington, DC) – Judicial Watch President Tom Fitton made the following statement regarding the appointment of U.S. Attorney David Weiss as special counsel by Attorney General Merrick Garland to investigate Biden family finances:
Attorney General Garland folded today, stopped ignoring DOJ regulations, and finally appointed a special counsel to investigate Hunter Biden and (indirectly) President Joe Biden for their corrupt family business dealings.
But appointing U.S. Attorney Weiss as special counsel, a man who tried to unethically slide Hunter’s corrupt plea deal past a federal judge is a sick joke. In fact, Mr. Weiss should be under investigation for his dishonest statements to Congress and his compromised, sweetheart plea deal for Hunter Biden.
Given the powerful and unrefuted testimony before Congress by senior IRS investigators that the criminal investigation of Hunter was obstructed by the Justice Department (when Weiss was nominally running the investigation) in order to protect Joe Biden, Weiss is the last person who should be special counsel.
Congress should speed up and escalate its investigations of Biden’s corruption, as the Justice Department is ethically broken.
In the meantime, Judicial Watch will continue its leadership role in investigating and exposing the worsening Biden corruption crisis through numerous FOIA and other federal and state legal actions.
Think about it. Weiss OBSTRUCTED the IRS criminal investigation to protect the Bidens. And now he’s the Special Council??? — TPR
US Attorney General Merrick Garland announced that US Attorney for Delaware David Weiss was appointed Special Counsel in the Hunter Biden investigation.
Weiss asked for special counsel status in the Hunter Biden case.
“This appointment confirms my commitment to provide Mr. Weiss all the resources he requests,” Garland said. “It also reaffirms that Mr. Weiss has the authority he needs to conduct a thorough investigation and to continue to take the steps he deems appropriate independently based only on the facts and the law.”
A reporter asked Merrick Garland why Weiss needed special counsel status if he already had the authorities he needed.
“If Weiss had the authorities he needed, why does he need to be a special counsel? Do you still have faith in U.S. Attorney Weiss after the [Hunter Biden] deal fell apart?” a reporter asked Garland.
Garland refused to answer any questions and walked away.
Recall David Weiss signed a June 7 letter claiming he had been granted “ultimate authority” over the Hunter Biden case.
“Delaware U.S. Attorney David Weiss told the House Judiciary Committee he had “been granted ultimate authority” over prosecutorial decisions related to the criminal investigation into Hunter Biden in a June 7, 2023, letter obtained by The Federalist. However, Weiss’s letter to Congress — and Attorney General Merrick Garland’s earlier testimony to the Senate Judiciary Committee that Weiss had “full authority” to charge Hunter Biden — directly conflicts with statements Weiss made to senior members of the team investigating the Biden son.” – The Federalist reported.
This contradicts what an IRS whistleblower heard David Weiss say during one of his in-person meetings with the prosecutor.
“Weiss said he tried to go to the DC US Attorney’s office and they wouldn’t approve it. And he was trying to go charge it elsewhere in California – and he was trying to seek special counsel authority and that got denied and so this was a shocker to the agents who were present,” Mark Lytle, an attorney for IRS whistleblower, previously told Fox News.
Merrick Garland, however, has insisted David Weiss had full authority to bring charges against Hunter Biden.
In March, Garland said under oath that Weiss had full authority to charge Hunter Biden.
“The U.S. Attorney in Delaware has been advised that he has full authority … to bring cases in other jurisdictions if he feels it’s necessary,” Garland said.
Merrick Garland recently said during a press conference that Weiss had full authority to make a decision to prosecute in any district he wanted to.
“As I said at the outset, Mr. Weiss was appointed by President Trump as the U.S. Attorney in Delaware and assigned this matter during the previous administration and would be permitted to continue his investigation and to make a decision to prosecute any way in which he wanted to and in any district in which he wanted to,” Garland said in June.
A general view of the Centers for Disease Control headquarters in Atlanta, Georgia
The U.S. Centers for Disease Control and Prevention (CDC) is still planning on recommending people receive a COVID-19 shot on an annual basis, the agency’s director says.
“We are likely to see this as a recommendation for an annual COVID shot, just like we have an annual flu shot,” Dr. Mandy Cohen, the director, said in a podcast episode released on Aug. 9. “And I think that will give more folks clarity about should they get one or not, because the answer is like, ‘Well, did you get one this year? If not, go get the new COVID shot.’”
She said that the CDC will likely make the recommendation in the coming weeks.
“This will be an annual vaccine … to make sure that you stay protected,” Dr. Cohen said.
Dr. Cohen was commenting after Rep. Brad Wenstrup (R-Ohio), chairman of the U.S. House of Representatives Select Subcommittee on the Coronavirus Pandemic, questioned her over what data would support annual shots and asked for a briefing on the matter.
Dr. Wenstrup gave the CDC until Aug. 16 to provide answers. The agency has not done so yet, a spokesperson for the panel said.
Dr. Cohen had said in July, in one of her first interviews after becoming the CDC’s director, that the agency was poised to recommend annual shots.
Waning Immunity
U.S. officials initially said people would only need a primary series to protect themselves against COVID-19 but in 2021, less than a year after recommending vaccination for virtually everyone, they authorized and advised boosters to try to stem waning immunity.
As newer variants have emerged, the vaccines have performed even worse, leading to recommendations for additional boosters and, in the fall of 2022, the clearance of updated bivalent shots from Pfizer and Moderna. Those shots later replaced the companies’ old vaccines.
The U.S. Food and Drug Administration (FDA), which decides whether to clear vaccines, said in June that it was directing Pfizer and other manufacturers to update the shots again to target the XBB.1.5 strain because the vaccines “appear less effective against currently circulating variants (e.g., XBB-lineage viruses) than against previous strains of virus.”
But XBB.1.5 has already been largely displaced by other variants, including EG.5. That undercuts the new strategy, Dr. Harvey Risch told The Epoch Times in an email.
“The boosters will be out-of-date before they are even released,” Dr. Risch, professor emeritus of epidemiology at the Yale School of Public Health, said. “As well, CDC has already said that efficacy of new boosters in preventing spread is transient and wanes, thus there is little reason to see the boosters as beneficial.”
A CDC spokesperson told The Epoch Times via email: “Dr. Cohen’s expert opinion is based on the science, which indicates that vaccine-induced immunity wanes and the COVID-19 virus is likely to continue to evolve. As she has said before, if the science changes, the agency will adapt its recommendations.”
The COVID-19 vaccines have never been 100 percent effective. No trial efficacy data exists for the currently available vaccines, but observational data indicate they provide transient protection against infection and severe illness, even turning negative after several months.
There is no evidence supporting the idea that the shots provide protection for one year.
“Federal mandates did not stop the spread or transmission of the COVID-19 virus. Should the CDC issue a recommendation for an annual COVID-19 vaccine, it will mark a significant change in federal policy and guidance regarding the COVID-19 vaccines and how they are utilized,” a spokesperson for the House panel told The Epoch Times via email. “Serious questions remain as to whether the science would support such a recommendation.”
In support of the planned recommendation, the CDC pointed to a modeling study and a seriesof other studieshighlightingwaningimmunity from the original shots, all of which were based on data from 2022 and earlier. The agency also cited a study that found the currently available boosters did not produce “robust neutralization” against newer variants.
Some of the papers concluded that people with so-called hybrid immunity, or vaccination on top of natural immunity, have the best protection. Other research has found that the latter protection, derived from recovering from COVID-19, is as good as or better than that from vaccines, though little data is available from recent months.
Timeline
Executives with Pfizer and Novavax have said they expect the FDA to authorize the new shots by the end of August. Moderna also makes a COVID-19 vaccine. Johnson & Johnson’s shot is no longer authorized.
After the FDA authorizes the latest formulations, the U.S. government plans to phase out the older shots. according to a planning document from the U.S. Department of Health and Human Services, the parent agency of both the FDA and the CDC.
The FDA has indicated it will not require trial efficacy data before authorizing the new shots but will monitor observational data, similar to its stance on the influenza vaccines.
After the authorizations, the Advisory Committee on Immunization Practices (ACIP), the CDC’s vaccine advisers, plans to meet to discuss for whom they will advise the CDC to recommend the shots. The CDC does not have to accept the advice, but often does.
“The FDA anticipates taking timely action to authorize or approve updated COVID-19 vaccines in order to make vaccines available this fall. After their authorization or approval, ACIP will meet to make a recommendation outlining use of these updated vaccines this fall,” the CDC spokesperson said.
The CDC has recommended, including in its latest slate of recommendations, that virtually every person receive a primary series. The CDC did ease up on booster recommendations in the most recent recommendations, saying some people did not need additional shots, in the first formal recognition of the high levels of natural immunity in the population.
Last week during an Australian Senate committee hearing, Pfizer and Moderna executives were grilled under oath about covid-19 vaccine policies and vaccine safety.
Tensions were high during the public hearing, which was live-streamed via the parliamentary website.
Senators fired questions at Pfizer and Moderna executives who responded by dodging questions and refusing to take accountability for their failures.
To complicate matters, the drug company executives did not attend the hearing in-person, only via video link allowing them to plead ignorance about the studies that were presented during the inquiry.
At the commencement, the Chair warned the witnesses against giving “false or misleading evidence” and after opening statements by Pfizer and Moderna, the floor was opened to questions.
Stopping transmission
Senator Matt Canavan began question time and was laser-focused on the issue of viral transmission.
“Did Pfizer test whether your covid-19 vaccine could stop or reduce the transmission of the virus before its approval and rollout in late 2020,” asked Canavan pointedly.
Pfizer Australia’s medical director Krishan Thiru was evasive.
Left to right: Brian Hewitt, Director of Regulatory Affairs, Pfizer Australia; Krishan Thiru, Medical Director, Pfizer Australia
“To bring this vaccine to patients we were required to show that the vaccine was safe and effective…The primary purpose of vaccination was, and remains, to protect the person who received the vaccine,” said Thiru.
Canavan reminded him that Pfizer’s own CEO Anthony Bourla told a reporter on NBC news on Dec 3, 2020, that it was “not certain” if vaccinated people could catch and spread the virus, but Thiru kept repeating the mantra, “the vaccine is safe and effective.”
Canavan persisted, citing Pfizer’s official tweet on Jan 14, 2023, stating its highest priority was its “ability to vaccinate at speed to gain herd immunity and stop transmission,” and then on June 8, 2021, Bourla tweeted, “the vaccine was a critical tool to help stop transmission.”
“What evidence did Pfizer have to make that public statement to imply that vaccination could stop transmission?” asked Canavan.
Thiru pleaded ignorance saying he was not familiar with the context of the tweets and took the question on notice (to respond later in writing).
Canavan explained that federal and state governments had imposed vaccine mandates based on the evidence and advice from the manufacturers that claimed the vaccines could “stop the spread.”
Canavan also pointed to the Doherty Modelling report submitted to national cabinet in Nov 2021 that underpinned the government’s decision to impose mandates in late 2021, but again, Pfizer could not confirm whether it was consulted about the modelling.
Hewitt said, “I can’t answer that question” and took it on notice.
Moderna Executive Director of Medical Affairs for Respiratory Vaccines Rachel Dawson, said that in the phase III pivotal trials of 2020, its mRNA vaccine showed that it could reduce symptomatic infection, and that it could “make an important contribution to reducing viral transmission.”
Dawson cited real world data demonstrating that the spread of the virus was reduced in households among vaccinated individuals and that they had a “lower viral load.”
But to this day, the US regulator says the ability of Moderna’s mRNA vaccine to reduce transmission remains unproven. “While it is hoped this will be the case, the scientific community does not yet know if Spikevax will reduce such transmission,” states the FDA.
Canavan said Moderna’s evidence, “just doesn’t seem to stack up”.
“Politicians told us it will stop the spread. Clearly that hasn’t happened. Do you have a simple explanation for why very high rates of vaccination, higher than anyone expected (90%) in this country, has clearly not stopped the spread of coronavirus,” asked Canavan.
But Moderna avoided the question on transmission, presumably because it would undermine the entire argument that vaccine mandates “keep others safe,” and instead, referred to its scripted statement that “the goal of vaccination is to prevent severe infection in hospitals.”
Preventing infection
Senator Gerard Rennick then proceeded to challenge Pfizer on its claim that the vaccine was “100% effective at preventing covid-19 cases,” a statement that Bourla tweeted on April 2, 2021.
Rennick proceeded to explain why the statement was implausible.
“By September 2022, Australia had recorded 10 million cases of COVID despite having an adult population vaccinated to the tune of 95% so given those real world figures in Australia, do you still stand by that statement?” said Rennick.
But Thiru responded repeatedly, “we strongly believe, and we reiterate, that the vaccine is safe and effective for its intended use” saying that Pfizer’s vaccine remained highly effective prior to the emergence of variants.
When Rennick asked Pfizer for its definition of “highly effective” in terms of duration, Thiru responded saying, “When the wild-type virus was prevalent, efficacy of approximately or greater than 90% was maintained at six months for illness and severe disease.”
But regulatory filings clearly show Pfizer had strong evidence by April 2021 that its vaccine’s efficacy waned, and withheld the data from the public for months.
Claiming that vaccine efficacy was 90% after six months following vaccination is misleading because that figure is largely driven by the first couple months of the trial when there was still a placebo group. Had people stayed in the trial for the whole duration of the 6 months, the average overall, would have been lower.
Lack of studies
Senator Rennick proceeded to read out the TGA’s non-clinical report listing all the safety studies in animals that were not carried out prior to testing in humans.
Despite assurances that “no corners were cut,” there were no carcinogenic tests, genotoxicity tests, immunotoxicity tests, duration studies, interaction studies with other medicines, and the list went on.
Again, Thiru predictably answered, “I don’t have that report in front of me, so I’m afraid I can’t talk to that.”
When Rennick asked directly if any studies were omitted or circumvented entirely to achieve the accelerated time frame for vaccine development, Pfizer objected saying its process was “thorough and comprehensive”.
Safety problems
Senator Rennick asked if Pfizer had determined the mechanism for why its vaccine could cause myocarditis and pericarditis, but Thiru was defiant saying that Pfizer had “strong confidence in the safety profile” of its vaccine.
Rennick would not let up. “I want you to explain to me why it causes myocarditis,’ he asked several times.
Thiru conceded that Pfizer was aware of “very rare” reports of myocarditis and pericarditis temporally associated with vaccination, but could not explain the mechanism, instead opting to take the question on notice again.
Senator Alex Antic challenged Pfizer on the Fraiman re-analysis, which found one additional SAE for every 800 people vaccinated with an mRNA vaccine, but his attempts hit a brick wall.
Senator Pauline Hansen chimed in, noting the Fraiman re-analysis found a “36% increase in serious adverse events. The most common were coagulation disorders, including thrombosis, and acute cardiac injury. In every 10,000 people injected 18 will experience a life threatening or altering medical complication,” said Hansen.
Again, Thiru pleaded ignorance. “I do not have a copy of your paper. I have not examined it,” he said, “the benefit risk ratio for vaccination remains strongly positive in all indications, all age groups for which it has been approved.”
Senator Hansen became visually frustrated.
“You haven’t read up on all of this, have you?” she said angrily, “You’ve come to this inquiry and you haven’t done anything whatsoever to respond to our questions. I think it’s very poor of you to not be able to answer these questions.”
When it was Moderna’s turn to respond to the Fraiman re-analysis, they too, said they were not aware of it.
Senator Antic asked Moderna what its overall rate of SAEs was for its mRNA vaccine and how that compared to routine vaccination.
But Moderna’s director of Scientific Leadership Chris Clarke said, “I don’t have the actual rates of adverse events,” as he shuffled through the papers on his desk.
Antic was staggered by the response, “You’re before a Senate inquiry and you cannot tell me the rates of serious adverse events? I mean, it’s quite extraordinary.”
Moderna took the question on notice and said that in the clinical trials they “observed no safety concerns.”
Indemnity agreements
Senator Malcolm Roberts asked for details of the indemnity agreement between Pfizer and the Australian government.
Specifically, Roberts asked if there was any clause in the agreement that indemnified Pfizer in the situation where an employee is mandated by their employer to undergo vaccination and then experiences harm.
“Senator, any indemnity agreements between Pfizer and the Australian Government are confidential, and we’re not able to discuss that in this forum,” responded Thiru.
Roberts fired back, “What have you got to hide?”
He also asked if there was any clause in the agreement that negates Pfizer’s indemnity in the event Pfizer is found to have committed fraud in the trial, as alleged by whistle-blower Brook Jackson in 2021.
“My question is simple. What is the answer? Yes or no?” asked Roberts. But Pfizer insisted “the contents of Pfizer’s contract with the Australian Government remains confidential.”
Senator Malcolm Roberts summed up his thoughts.
“You have repeatedly refused to provide evidence and dodged questions from Senators Rennick and Antic. You have relied instead on appeals to authority, and other logical fallacies.”
Covid vaccine in pregnancy
Senator Hansen confronted Pfizer with questions about the safety of its vaccine in pregnant and breastfeeding women.
Thiru did concede that there is limited clinical trial evidence in pregnant women, but said that peak bodies such as the Royal Australian and New Zealand College of Obstetricians and Gynaecologists (RANZCOG) supported use of the vaccine.
“[RANZCOG] have said pregnant women in Australia are a priority group for covid-19 vaccination and should be routinely offered the Pfizer vaccine (Comirnaty) or Moderna (Spikevax) vaccines at any stage of pregnancy. They have said there is no evidence of increased risk of miscarriage or teratogenic risk with mRNA or viral vaccines.”
Forced vaccination
One of the most egregious moments of the hearing was when Pfizer’s Head of Regulatory Affairs Brian Hewitt, piped up and said no-one in Australia was ever “forced” to be vaccinated.
Senator Hansen took exception to the comment and asked if Hewitt would retract his statement.
Hewitt held his position saying, “No. I believe firmly that nobody was forced to have a vaccine.”
“A lot of Australians will disagree with you on that one,” retorted Senator Hansen.
Senator Matt O’Sullivan was incredulous. He said that in his state of Western Australia, there were mandates across the board, with “very, very few exceptions.”
“If you wanted to go to work, and earn a living and provide for your family, you had to be vaccinated. I am staggered that that was your response to questions in relation to whether or not people were forced to have vaccines,” said O’Sullivan.
Many of O’Sullivan’s constituents had to go without income because the state government was “forcing” them to be vaccinated against their will.
Hewitt looked down to read a pre-prepared answer, much to the dismay of listeners.
“Senator, mandates, and vaccine requirements are determined by governments. As a company we were not involved in any government vaccine mandates. I don’t believe the mandates actually forced individuals to get vaccinated.”
Pfizer did confirm that it enforced a vaccine mandate within its own company and that it had imported a special batch of covid-19 vaccines for its employees. Why the special batch? “So that no vaccine would be taken from government stocks,” said Hewitt.
Thiru also said there were some exemptions for medical or religious reasons and that “a small number of colleagues departed the company,” presumably because they did not comply with the mandate.
Moderna, on the other hand, distanced itself from commenting on vaccine mandates.
Clarke, Director, Scientific Leadership, Moderna.
Moderna’s Vice President of Medical Affairs Jane Leong said, “We do not have a view on decisions taken by public health agencies or governments in relation to vaccine mandates. This is purely a matter for policymakers.”
At the finish line, Pfizer and Moderna executives managed to expertly dodge questions, they couldn’t recall their own rate of SAEs, they wouldn’t admit that covid vaccines cannot stop transmission, and they refused to divulge details of their indemnity agreements with the government.
Responses to questions on notice are due Aug 17, 2023.
This article comes from the “BuzzLoving.com” website and is written by a Trump-hating leftist calling itself “Milla” — you can see all 81 pages of articles it’s written by going HERE.
“Return to the ‘whites-only’ luncheonettes of the 1960s South” – US Supreme Court strikes blow against LGBTQ+ rights.
–Original Article headline
Before I get into the article proper, let me state my personal opinion to the rainbow community at large.
You have the right to be whatever you chose to be. Just like I have the right to be myself. You DON’T have the right to demand that I think your way and kowtow to your fantasies on penalty of being beaten, killed or labeled a bigot, a Nazi, or any other derogatory term you come up with. I don’t have the right to sue you for being what you chose to be, but you don’t have the right to try to enforce your fantasies on me via a lawsuit, either. You respect me, I’ll respect you, even if we don’t agree on life choices. Simple. That’s the way a mature person behaves.
End of disclaimer.
The Supreme Court ruled in favor of an evangelical Christian web designer from Colorado who refused to work on invites for same-sex marriage, giving a significant blow to the rights of LGBTQ couples.
The Supreme Court cited free speech.
Evangelical Christian web designer Lorie Smith has a free speech right under the Constitution’s First Amendment to decline to endorse messages she disagrees with, it has been decided. This one decision could cause other owners of similar creative businesses to evade penalties under laws in 29 states that defend the rights of the LGBTQ community. (Notice the defendant is a biological woman. –TPR)
The statement from the Justice
Justice Neil Gorsuch wrote, “The First Amendment envisions the United States as a rich and complex place, where all persons are free to think and speak as they wish, not as the government demands.” He added, “At the same time, this court has also recognized that no public accommodation law is immune from the demands of the Constitution. In particular, this court has held public accommodations statutes can sweep too broadly when deployed to compel speech.”
Shutterstock photo
Smith sued on hypothetical grounds.
Smith opposes same-sex marriage on religious grounds and sued the state in 2016 because she said she would like to accept customers planning opposite-sex weddings but reject requests made by same-sex couples. She was never disciplined for declining a same-sex couple, and it’s unclear if she ever did. Instead, she sued on hypothetical grounds.
(THIS IS NOT “HYPOTHETICAL” Colorado anyone? And the author’s painfully obvious bias is on full display here.–TPR)
Smith celebrated, but many expressed worry and dread.
(How many is “many” there, cupcake? — TPR)
“This is a victory not just for me but for all of us; whether you share my beliefs or completely disagree with them, free speech is for everyone,” Smith told the press. But Justice Sonia Sotomayor argued that this was a backlash to the movement for liberty and equality for gender and sexual minorities” and a type of “reactionary exclusion,” calling it “heartbreaking.”
“Return to the ‘whites-only’ luncheonettes.”
Former U.S. Attorney and Deputy Assistant Attorney General Harry Litman shared that this was a major blow to human rights, writing, “Return to the ‘whites-only’ luncheonettes of the 1960s South & posit that the owners attest that they have sincere religious beliefs, reinforced by their pastor every Sunday, that Blacks are inferior and that serving them would force them to endorse a message they disagree with..” Litman added, “That’s where we are headed.”
(Oh oh, Not kowtowing is “racist” now, is it? *facepalm*– TPR)
“The opinion is out there like a loaded gun.”
The lawyer also clarified, “To be clear, I’m not saying that’s where we are headed, although to paraphrase Justice Jackson, the opinion is out there like a loaded gun for someone who wants to go that way. The point for today is just that the opinion doesn’t have a limiting principle that forecloses that result.”
(Bloviate much? Oh, I forgot, you’re not only a person with a law degree, but you’re also a bureaucrat. Silly me. –TPR)
Another important takeaway
Time wrote, “Put plainly: states can try to pass local anti-bigotry laws, but national religious liberties still supersede them.” The publication also connected how the ruling came a year after the fall of Roe v. Wade, and Court watchers predicted that things would only get worse for women as well as LGBTQ rights.
(“For women?” Really. Sorry, that just won’t wash. Maybe for those females who are still emotional babies, but not for anyone who accepts the responsibility for their own actions. –TPR)
The York fire burns in the Mojave National Preserve in California on Sunday, July 30.
Reported by CNN. (Sometimes they do good work.)
Firefighters battling a large whirl-spawning wildfire in California and southern Nevada are facing challenging conditions as the blaze spreads and threatens iconic desert Joshua trees.
The York Fire – already California’s largest fire of the year – has burned more than 82,000 acres as of Wednesday morning, fire officials said. It began Friday in the New York Mountains of California’s Mojave National Preserve and crossed state lines into Nevada on Sunday.
Crews have been battling the flames under unpredictable wind patterns and unrelenting heat, authorities said. They’ve also been trying to not disturb desert tortoises – federally listed as a threatened species – in part by trying to avoid their burrows.
The fire, among dozens burning around the country under scorching temperatures, has been fueled by extreme conditions that have made it more dangerous and difficult to control, fire officials said Monday night. The York Fire was 30% contained as of Wednesday morning.
The York Fire has burned more than 80,000 acres.
The blaze has spawned fire whirls – “a vortex of flames and smoke that forms when intense heat and turbulent winds combine, creating a spinning column of fire,” the Mojave National Preserve said Sunday. As the fire-heated air rises, cold air dashes to take its place, creating a spinning vortex rising from a fire and carrying aloft smoke, debris, and flame – also referred to as a fire tornado in some cases.
Firefighters also were seeing 20-foot flames in some areas, according to Mojave National Preserve authorities.
The fire is also threatening groves of Joshua trees – the branching, spiky plants of the Mojave Desert that can live more than 150 years.
“It will take a lifetime to get those mature Joshua trees back,” Laura Cunningham, the California director of the Western Watersheds Project, told CNN affiliate KVVU. “Some are fire resistant, and if the flames are not too hot, they will stump sprout out or reseed.”
“This is pretty devastating,” Cunningham said.
The Mojave National Preserve has been seeing an increase in fire frequency over the past decade due to a combination of wet winters and increasing levels of invasive grasses, fire officials say on Inciweb, a clearinghouse for US fire information.
“If an area with Joshua trees burns through, most will not survive and reproduction in that area is made more difficult,” the National Park Service says. “Wildfires could also result in the loss of irreplaceable resources in the park, like historic structures and cultural artifacts.”
In 2020, a 43,273-acre wildfire burned through the Joshua tree woodland of California’s Cima Dome, destroying as many as 1.3 million Joshua trees and leaving behind a plant graveyard, according to the National Park Service.
Firefighters braving intense desert heat to stop the York Fire’s spread in the Mojave National Preserve are among more than 11,000 wildland firefighters and personnel assigned across the country, the National Interagency Fire Center said Tuesday.
Fifty-six active, large fires were burning in 11 states as hot and dry conditions persist throughout the US, the center said Tuesday. More than 1.1 million acres have burned across the US in 2023 as of Tuesday, the center said.
Emerging desert tortoises pose unique challenge
Firefighters were aided by a brief but heavy downpour early Tuesday as they worked to contain the York Fire. More rain moved across the area early Wednesday and may give firefighters an additional boost.
But rain in the Mojave Desert, which is seasonal and scarce, “poses a unique challenge to firefighters,” the Mojave National Preserve said.
Desert tortoises – federally listed as a threatened species – become especially active on wet summer days, emerging from their burrows to drink rainwater.
“Fire crews carefully balance fire suppression with resource protection. They will be on the lookout for desert tortoises, making sure to avoid burrows and active individuals,” the Mojave National Preserve said.
The good news is that most desert wildlife can move to safety when fire approaches, park officials said.
“Resource staff at Mojave National Preserve anticipate that the York Fire has caused minimal damage to critical tortoise habitat and has likely affected few individuals since tortoise observations in the fire area are rare,” preserve staff said.
