Saturday, June 25, 2022
Merrick Garland’s Department Of Justice Is A Threat To The Republic
Federal raids this week, along with an inappropriate statement about a SCOTUS ruling, underscore the weaponization of the DOJ under Garland.
It’s become painfully obvious over the past year that the Justice Department under Attorney General Merrick Garland has been weaponized and politicized to the point that it represents an active threat to the rule of law and the separation of powers. It’s not too much to say that Garland’s DOJ has become a threat to the republic.
Just take this past week. On Thursday, following an historic 6-3 U.S. Supreme Court ruling that struck down a New York law for violating state residents’ Second Amendment rights, a DOJ spokeswoman released a statement saying “we respectfully disagree” with the ruling.
The ruling is of course a great victory for the Constitution and a long-overdue vindication of New Yorkers’ Second Amendment rights. The law in question had been on the books for more than a century, and made it nearly impossible for ordinary people to obtain a concealed-carry license, The unconstitutional law forced New Yorkers to prove to a municipal bureaucrat that they needed a gun for self-defense. In practice, this made it almost impossible for law-abiding citizens in New York to exercise their constitutional right to bear arms.
But neither the law in question nor the Supreme Court’s decision implicates federal gun laws in any way. There is no reason for the DOJ to weigh in on the matter or express any opinion whatsoever on the ruling. Only an utterly politicized Justice Department hoping to undermine the Supreme Court’s constitutional authority and sow the seeds of nullification would issue such a statement.
That made Clark a target for the House Democrats’ Jan. 6 committee, whose Soviet-style show trial spent a good deal of time Wednesday implying that Clark, who once oversaw 1,400 lawyers and two divisions at DOJ, is traitor who tried to overturn the results of the election.
This should come as no surprise, since the entire raison d’être of the Jan. 6 committee is to smear anyone who questioned the outcome of the election or raised concerns about its unprecedented irregularities as a coup-plotter responsible for the Jan. 6 “insurrection.” In fact, Clark’s only crime is that in a sea of attorneys who didn’t want to lift a finger to investigate the election, he looked for options and fought to uncover the truth.
Of course, he’s not the only one the DOJ targeted this week. The same day Clark’s house was raided, FBI agents raided the home of Michael McDonald, Nevada’s top GOP official.
His crime, according to the Justice Department and the Jan. 6 committee, was signing a document with five other Nevada Republican Party electors after the 2020 election signaling their support for Trump. Among the signatories of the purely symbolic document was state GOP secretary James DeGraffenreid, whom FBI agents tried but failed to...
The 90 Miles Mystery Video: Nyctophilia Edition #1060
Before You Click On The "Read More" Link,
Please Only Do So If You Are Over 21 Years Old.
If You are Easily Upset, Triggered Or Offended, This Is Not The Place For You.
Please Leave Silently Into The Night......
The 90 Miles Mystery Box: Episode #1760
You have come across a mystery box. But what is inside?
It could be literally anything from the serene to the horrific,
from the beautiful to the repugnant,
from the mysterious to the familiar.
If you decide to open it, you could be disappointed,
you could be inspired, you could be appalled.
This is not for the faint of heart or the easily offended.
You have been warned.
Friday, June 24, 2022
Covid Vaccines More Likely to Put You in Hospital Than Keep You Out, BMJ Editor’s Analysis of Pfizer and Moderna Trial Data Finds
A new paper by BMJ Editor Dr. Peter Doshi and colleagues has analysed data from the Pfizer and Moderna Covid vaccine trials and found that the vaccines are more likely to put you in hospital with a serious adverse event than keep you out by protecting you from Covid.
The pre-print (not yet peer-reviewed) focuses on serious adverse events highlighted in a WHO-endorsed “priority list of potential adverse events relevant to COVID-19 vaccines”. The authors evaluated these serious adverse events of special interest as observed in “phase III randomised trials of mRNA COVID-19 vaccines”.
A serious adverse event was defined as per the trial protocols as an adverse event that results in any of the following conditions:
- death;
- life-threatening at the time of the event;
- inpatient hospitalisation or prolongation of existing hospitalisation;
- persistent or significant disability/incapacity;
- a congenital anomaly/birth defect;
- medically important event, based on medical judgement.
Dr. Doshi and colleagues found that the Pfizer and Moderna mRNA COVID-19 vaccines were associated with an increased risk of serious adverse events of special interest of 10.1 events per 10,000 vaccinated for Pfizer and 15.1 events per 10,000 for Moderna (95% CI -0.4 to 20.6 and -3.6 to 33.8, respectively). When combined, the mRNA vaccines were associated with a risk increase of serious adverse events of special interest of 12.5 per 10,000 vaccinated (95% CI 2.1 to 22.9).
The authors note that this level of increased risk post-vaccine is greater than the risk reduction for COVID-19 hospitalisation in both Pfizer and Moderna trials, which was 2.3 per 10,000 participants for Pfizer and 6.4 per 10,000 for Moderna. This means that on this measure, the Pfizer vaccine results in a net increase in serious adverse events of 7.8 per 10,000 vaccinated and the Moderna vaccine of 8.7 per 10,000 vaccinated.
Addressing the difference between their findings and those of the FDA when it approved the vaccines, the authors note that the FDA’s analysis of serious adverse events “included thousands of additional participants with very little follow-up, of which the large majority had only received one dose”. The FDA also counted ‘people affected’ rather than individual events, despite there being twice as many individuals in the vaccine group than in the placebo group who experienced multiple serious adverse events.
The authors wonder where the U.S. Government’s own studies of adverse events are. They note that in July 2021, the FDA reported detecting four potential adverse events of interest following Pfizer vaccination – pulmonary embolism, acute myocardial infarction, immune thrombocytopenia and disseminated intravascular coagulation – and stated it would...
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