Legalizing And Regulating Drugs Is The Only Way Out Of The Overdose Crisis

Should heroin and cocaine be legally available to people who need and want them? If we are serious about stopping the crisis of drug overdose deaths, that is exactly the kind of profound change we need. Yes, extensive regulations would be necessary. In fact, the whole point of regulating drug production and sales is that we can better control what is being sold and to whom.

After British Columbia’s Provincial Health Officer Dr. Bonnie Henry testified to the all-party health committee in Ottawa in May that regulating these controlled drugs would minimize harms, B.C. Premier David Eby said he disagreed. He is quoted saying that “in a reality-based, real-world level, (it) doesn’t make any sense.” But does our current approach of drug prohibition “make sense?”

Since the overdose crisis was declared in 2016, illicit drug toxicity deaths have become the leading cause of unnatural death in B.C. and the leading cause of death from all causes for those aged 10 to 59. More than 44,000 people have died from drug poisoning in Canada since 2016, and more than one-third of those were in B.C. An average of 22 people are dying every day in Canada because the illicit supply of drugs is toxic.

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Senate Joins House in Proposal for ‘Automatic’ Draft Registration

Contrary to earlier reports, the U.S. Senate has joined the House of Representatives in moving toward a foolhardy attempt to ‘automatically’ register all draft-eligible U.S. citizens and residents for a possible military draft, by extracting and aggregating information obtained from other Federal agencies.

The proposal for “automatic” draft registration is among several previously-undisclosed provisions related to Selective Service in the newly-release version of the National Defense [sic] Authorization Act (NDAA) for Fiscal Year 2025 approved by the Senate Armed Services Committee (SASC) and to be considered by the full Senate.

The 1,197-page SASC proposal for this year’s NDAA was approved by the committee in closed session last month, and only a summary was released. At the time, a spokesperson for the SASC told me that if “automatic” Selective Service registration had been included in the bill, it would have been included in the summary. That proves to have been incorrect: The proposal for “automatic” draft registration was included in the SASC version of the bill, but not in the summary.

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GOP Congressional Committee Approves Bill To Block Marijuana Rescheduling, While Rejecting State Cannabis Protections Amendment

A key GOP-led House committee has approved a large-scale spending bill that would block the Justice Department from rescheduling marijuana, while also amending a longstanding rider protecting medical cannabis states from federal interference by adding new language to authorize enhanced penalties for sales near schools and parks. Members also rejected an amendment that would have extended those protections to all state and tribal cannabis programs, including those allowing recreational use and sales.

At a House Appropriations Committee hearing on Tuesday, the panel passed the legislation covering Commerce, Justice, Science, and Related Agencies (CJS) with the hostile marijuana provisions attached.

The bill as approved in committee would block the Justice Department from using its funds to reschedule or deschedule marijuana. This comes amid an active rulemaking process to move cannabis from Schedule I to Schedule III of the Controlled Substances Act (CSA), as DOJ formally proposed earlier this year.

SEC. 623. None of the funds appropriated or other wise made available by this Act may be used to reschedule marijuana (as such term is defined in section 102 of the Controlled Substances Act (21 U.S.C. 802)) or to remove marijuana from the schedules established under section 202 of the Controlled Substances Act (21 U.S.C. 812).

GOP senators have separately tried to block the administration from rescheduling cannabis as part of a standalone bill filed last September, but that proposal has not received a hearing or vote. Including such a ban in key annual spending legislation is a way for opponents to force the issue forward. It’s far from clear that the Democratic-controlled Senate would go along with proposal, however.

The legislation as approved by the panel on Tuesday still includes a longstanding rider to prevent DOJ from using its funds to interfere in the implementation of state medical marijuana programs that has been part of federal law since 2014, but the committee added new language stipulating that the Justice Department can still enforce a section of U.S. code that calls for increased penalties for distributing cannabis within 1,000 feet of an elementary school, vocational school, college, playground or public housing unit.

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Klaus Schwab Says Humanity Must Be “Forced Into Collaboration” With Globalist Elites

Speaking at the WEF’s ‘Annual Meeting of the New Champions’, often dubbed the “Summer Davos,” in China, Schwab stated that in order to drive the “Fourth Industrial Revolution” forward, elites must aggressively drive their agenda home.

“To drive future economic growth we must embrace innovation and force the collaboration across sectors, regions, nations, and cultures to create a more peaceful, inclusive, sustainable, and resilient future,” Schwab proclaimed.

He added, “At this critical juncture the active participation of all stakeholders is essential to ensure a sustainable development path.”

In another clip, Schwab touted AI and other technologies becoming ubiquitous as a reason why humanity must “work together” with the global elite.

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Supreme Court Rejects Challenges to COVID-19 Shot Mandates

The U.S. Supreme Court has rejected appeals to two COVID shot mandate-related cases brought by Children’s Health Defense (CHD). In one case, CHD appealed a lower court ruling that the non-profit group lacked standing to sue the U.S. Food and Drug Administration (FDA) over its authorization of the COVID-19 shots for young children. In the other case, CHD challenged the COVID shot mandate for students at Rutgers University in New Jersey.1

The Supreme Court did not issue an explanatory statement along with their denial of these appeals.2 By refusing to hear the cases, the Supreme Court has allowed the opinions of the lower court to stand.3

Appellate Court Dismissed CHD’s Claims Against the FDA

CHD, together with five sets of parents, sued the FDA over its emergency use authorization COVID shots for minors. The District Court dismissed the case finding that the Plaintiffs did not have standing to sue and the 5th Circuit Appellate Court affirmed that ruling. Plaintiffs alleged that when the FDA granted pharmaceutical companies an Emergency Use Authorization (EUA) to distribute the experimental biologicals, it did not adhere to the requirements of the Administrative Procedures Act (APA) reasoned decision-making requirements. Plaintiffs sought an injunction forbidding the marketing or promotion of the shots.4

A Plaintiff will have standing to sue when it has been demonstrated that the Plaintiff has suffered an injury in fact that is, “concrete, particularized, and actual or imminent;” the defendant caused the injury; and the injury would likely be redressed by the court.5 The injury must also be concrete, which has been defined as “whether the alleged injury to the Plaintiff has a ‘close relationship’ to a harm ‘traditionally’ recognized as providing a basis for a lawsuit in American courts.”6

The Appellate Court agreed with the District Court that the Plaintiffs did not satisfy their burden of showing that their injury was concrete, particularized or imminent, rather than merely speculative.

The Appellate Court wrote:

To begin, it is insufficient that Plaintiff allege that some hypothetical third party might, at some hypothetical point in the future and through some hypothetical means, will vaccinate their children against their wishes.7

The Appellate Court added that CHD also lacked standing because the organization has not “diverted significant resources to counteract” the EUA granted to the COVID shots by the FDA. The Appellate Court ruling went on to state that the Plaintiff also has not shown that the FDA’s authorization, “concretely and ‘perceptibly impaired’” its ability to fulfill their mission. The courts dismissed the action due to lack of standing.8

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Outraged Citizen Unleashes on City Council For Passing One of the Nation’s Toughest Hate Crime Laws

Coeur d’Alene, Idaho, now has one of the nation’s toughest hate crime laws.

The Coeur d’Alene City Council unanimously approved a new hate crime ordinance, introducing a significant addition to the municipal code. 

This new chapter establishes a separate offense for individuals who commit an existing offense with a bias motive, Krem2 reported.

The Idaho Tribune described the law as “draconian,” arguing it “will basically make it illegal to think the wrong way.”

“If found guilty, you’ll be sentenced to ‘[re]education.’”

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Court: Doctors Threatened For Questioning The Covid Regime Can Sue Tyrannical Credentialing Boards

In a landmark case, an appellate court judge has ruled that physicians threatened by credentialing boards for speaking out against Covid policies and abortion have sufficient standing in court.

A year after the case was dismissed by a district court, the Association of American Physicians and Surgeons (AAPS) Educational Foundation filed an appeal for the right to sue the American Board of Internal Medicine, the American Board of Obstetrics and Gynecology, the American Board of Family Medicine, and the secretary of the U.S. Department of Homeland Security for “coordinated” attempts to “censor and chill the speech of physicians,” especially those “who spoke critically of positions taken by Dr. Anthony Fauci, lockdowns, mask mandates, Covid vaccination, and abortion.”

A district court judge had ruled AAPS lacked standing and denied AAPS’s attempt to amend the claim. But in a decision filed June 3, the U.S. Court of Appeals for the 5th Circuit reversed the dismissal, and the case has now been remanded to a lower court for discovery and potentially a full trial.

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Michigan and Penn. Capitol Sent Bomb Threats, Staffers Blame the FBI

The Michigan and Pennsylvania state capitols were both evacuated on Sunday after receiving bomb threats, “in the name of Palestine,” but some doubt the threats were genuine, blaming the FBI instead.

The Gateway Pundit spoke to Michigan State Rep. Steve Carra, who said that the threat, if genuine, demonstrates the left’s commitment to political violence. The Michigan capitol has been the scene of angry pro-Palestine demonstrations in recent months.

“The radical left threatens death and destruction in an attempt to get their way and plants operatives at conservative rallies to incite violence, making it look like conservatives are extremists. Then government and the mainstream media pushes their narrative over the truth,” he said.

Rep. Carra continued that the threat could just as easily have been another operation led by the FBI, like the Gretchen Whitmer “kidnapping” plot, to sow confusion and political division.

He described such behaviour as “treasonous activity” and added, “quite frankly it’s repulsive that mainstream media aids and abets this dangerous behavior by peddling disinformation narratives instead of reporting on facts.”

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How do you know the FDA is a captured agency?

How sweet—the FDA shows us a multiracial July 4 barbecue, warning us about the possibility of food poisoning when sharing food with friends. (I had to chop off the heads of the partiers so the page would fit on the screen, but believe me there was a red, white and blue theme.)

Of all the issues FDA has to deal with: food, drugs, medical devices, cosmetics, what do you think might be most important? What do you want to tell the public about?

Maybe drug shortages, or drug recalls? Drug side effects? Food recalls? Medical device problems? New drug approvals?

Nope.

First we get the kindergarten lessons, telling us the difference between hot foods and cold foods. Message: worry about your food.

Second, we hear about avian flu, though no one has ever caught avian flu from eating or drinking anything. Let no opportunity to scare people about avian flu get wasted! If you click on the page you get a bunch of fluff and this:

Collectively, these studies provide strong assurances that the commercial milk supply is safe.”  So why even mention it?

Third, we are told to stop the spread of misinformation. Did you know that FDA has a Rumor Control service where you can be helped to snitch to social media companies about misinformation on their platforms? Isn’t this a First Amendment violation? Who knows, these day?

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120+ years of legalized, US-government-led pharmaceutical fraud.

Since December 2023, I’ve researched and written a series of reports1 tracking the development of federal Congressional laws and federal agency non-regulations that have non-regulated the licensing and manufacture of biological products and vaccines from 1944 to the present.

The series so far focuses on the period since 1972, when the fake biological product regulation program was fake-transferred from NIH to FDA.

The record of laws passed by Congress, signed by US Presidents, implemented through the US Code of Federal Regulations, with rule changes published in the Federal Register, and upheld by federal and state courts, confirm that biological product and vaccine licensing, cGMP-compliance monitoring and related programs allegedly operated by the US Food and Drug Administration have been nothing more than pretextual, deceptive acts carried out to elicit and maintain broad public compliance with vaccination programs, because vaccines are actually intentionally harmful biological weapons developed, manufactured, promoted and distributed jointly by the federal Public Health Service and pharmaceutical companies, and vaccinators don’t want targets to know it.

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