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Doctors Group Launches Campaign Empowering More Healthcare Professionals To Join Drug Decriminalization Movement

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A group of doctors who support drug policy reform is launching a new campaign aimed at equipping physicians and healthcare professionals with skills to play a greater role in advocating for the decriminalization of drugs. Organizers say there’s a need for more voices from the medical community to take part in ongoing discussions around cannabis, psychedelics and harm reduction issues.

Doctors for Drug Policy Reform (D4DPR) says it’s spent the past year developing its new advocacy toolkit intended for healthcare professionals and scientists on “Transitioning from a Criminal Justice Model of Drug Use to a Health-focused Approach.” It includes guides to help would-be activists craft opinion pieces and engage with lawmakers and the media in order to “educate on the failures and lasting harms of the War on Drugs” and “confidently reframe drug use through a compassionate public health lens.”

“We’re assembling a core group of ‘on-call’ health professionals who are willing to lend their voice when timely advocacy opportunities arise,” says a recent D4DPR email about the effort, funded through a grant from the Drug Policy Alliance (DPA). “Now more than ever, we need healthcare professionals like you to speak up—especially when critical legislation is being debated.”

Bryon Adinoff, D4DPR’s president, told Marijuana Moment that it’s “imperative” that healthcare professionals take part.

“We want to health them speak up and learn how to do it in the right way,” he said.

Among the topics D4DPR is prioritizing with the new initiative are cannabis regulation, the decriminalization and therapeutic use of psychedelics as well as overdose prevention centers. By and large, Adinoff said, other medical professionals and organizations have “not been sufficiently active in this area.”

“Prohibition in general has really hurt individuals and communities around the world,” he said. “We’re obligated to speak up.”

In addition to guidance for how to engage in advocacy, the new D4DPR toolkit includes factsheets, a book of best advocacy practices and ways to connect with other advocates.

“Your insight and credibility can help shift public opinion, influence public policy, and reduce the stigma that harms our patients,” the group’s email to supporters says. “Together, we can create drug policies rooted in science, dignity, and care.”

Adinoff pointed out that health professionals are in a powerful position to influence public opinion, noting that “rightly or wrongly, survey after survey, we show up as the most trusted voice.”

“People believe us,” he said. “Even in this time of anti-science, I still think we have a better likelihood of being trusted to do the right thing—and say the right thing—compared to most other professions.”

D4DPR is asking would-be advocates to send an email to learn more about the new program.

The new advocacy push adds to other efforts the group has taken up in order to influence public policy. In March, for example, D4DPR published a position paper calling for states to decriminalize personal use and possession of an array of psychedelic substances.

“Criminalizing the personal use and possession of psychedelics is a costly misuse of resources,” it contends. “A cohesive state-level decriminalization framework would better align with evidence-based drug policies, ensuring a more just and effective response to substance use.”

The decriminalization white paper came on the heels of another D4DPR position paper about treatment strategies for opioid use disorder. That paper, by Hunter Platzman, argues that rather than rely agonist treatments such as methadone and buprenorphine, policymakers should embrace additional safer supply interventions, such as prescribing pharmaceutical-grade heroin.

While agonist treatments are legal, well established treatments, that paper argues, they’re used by fewer than 35 percent of people with opioid use disorder. Others are either unable to access the therapies or refuse them altogether. Prescription heroin, Platzman argues in the report, “demonstrates superior efficacy compared to traditional medications like methadone” and is far less lethal than highly toxic synthetic opioids, such as fentanyl.

In April of last year, meanwhile, D4DPR argued in a separate position paper that hemp-derived cannabinoids should be regulated more like marijuana.

“Our understanding of these compounds is limited,” the paper said of compounds like delta-8 THC. “Many have never been observed in nature and their toxicology is unknown.”

“Our stance at D4DPR,” it continued, “is that all intoxicating cannabinoids should be subject to a regulatory framework to ensure public safety.”

The cannabinoids paper was an attempt to bridge what the group described as a policy gap between between hemp—legalized federally through the 2018 Farm Bill—and marijuana, which remains federally illegal.

“The reason we got into this problem is by making this artificial distinction between two plants, hemp and cannabis, that are identical plants. One has low amounts of THC and one doesn’t,” Adinoff told Marijuana Moment at the time. “That’s what got us into this mess.”

D4DPR was long known as Doctors for Cannabis Regulation (DFCR) but rebranded in 2023 to reflect a growing focus on “a wider range of drug policy issues beyond cannabis,” including psychedelics and broader harm reduction matters, leaders said at the time.

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Advocacy Organizations Call on Meta to End Censorship of Cannabis and Psychedelic Communities

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In a letter to Meta Platforms, Inc., the parent company of Facebook and Instagram, a group of cannabis and psychedelic advocacy organizations, led by Students for Sensible Drug Policy (SSDP), called on the company to end what it describes as “ongoing and disproportionate censorship of content related to cannabis, psychedelics, and harm reduction.”

“Accounts committed to public education, legal and policy advocacy, research dissemination, and harm reduction services — including those of licensed healthcare professionals, nonprofits, and legal businesses — have been routinely shadowbanned, deplatformed, or had their posts removed with little explanation or recourse, despite operating in full compliance with local laws. This suppression is not merely an inconvenience; it is a form of digital marginalization.” — SSDP, in the letter

The groups argue the censorship of cannabis and psychedelics continue amid accelerating overdose deaths and mental health crises, and call on Meta to “end discriminatory bans and shadowbans,” “establish clear, transparent, and consistent content policies that distinguish between promotion of the sale of illegal substances and legitimate drug education and advocacy,” “create a dedicated appeals and accountability process specific to drug-related content that includes community stakeholders and subject-matter experts,” and “engage in regular dialogue with the psychedelic, cannabis, and harm reduction communities to better understand our work and co-create equitable guidelines for content moderation.”

In all, 81 organizations, consisting of students, educators, researchers, advocates, entrepreneurs, and community leaders, joined the letter, calling Meta’s policy “censorship of science, public health, legal, and public policy discourse” and describing the policy as “not an act of neutrality.”

“As the cultural and legal landscapes around these issues evolve,” the letter states, “so too must your policies.”



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Florida Removes Nearly 11,000 Hemp Product Packages for Violating Child-Protection Standards

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Florida officials have removed nearly 11,000 packages of hemp products for violating child-protection standards for packaging, labeling, and marketing throughout the state during the Florida Department of Agriculture’s “Operation Safe Summer.”

In a statement, Commissioner of Agriculture Wilton Simpson said the agency has “drawn a hard line in Florida when it comes to protecting our children from dangerous and deceptive hemp products.”

“’Operation Safe Summer’ is our latest effort to crack down on bad actors who think they can skirt the law, ignore public safety, and profit off high-potency, intoxicating hemp products that endanger our children. We will not tire in our commitment to cleaning up this industry, holding violators accountable, and sending a clear message: if you refuse to follow the law, you won’t be doing business in Florida.” — Simpson in a press release

The agency in April and June advised businesses in April and June about the planned enforcement of new Agriculture Department rules around intoxicating hemp-infused products. The new rules, enacted in 2023, include:

Prohibition on specified color additives.

Mandatory child-resistant packaging in accordance with ASTM International D 3475-20, Standard Classification of Child Resistant Packages.

Certificates of analysis must now include laboratory information, the concentration of total delta-9 THC, and confirm the presence or absence of prohibited substances and pathogens.

Restrictions on marketing and advertising of hemp and hemp extract intended for human consumption.

Enhanced labeling requirements, including the use of common household measurements for serving sizes and the provision of a scannable barcode or QR code, must link to the certificate of analysis within three or fewer steps.

Water activity for cannabis flower or leaves must be 0.60 (±0.05).

Since July 2023, the Agriculture Department has uncovered more than 738,000 packages of hemp products in violation of child-protection standards.



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Nebraska Officials Propose Emergency Medical Cannabis Regulations

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The Nebraska Medical Cannabis Commission last week approved emergency regulations to begin accepting medical cannabis applications as soon as Gov. Jim Pillen (R) allows the agency to proceed, the Nebraska Examiner reports. Under the state’s voter-approved medical cannabis law, the commission must start accepting applications by July 1.

The regulations largely mirror a legislative proposal that failed in the legislature last month and would remain in effect for 90 days after being approved by the governor.

Under the medical cannabis law, medical cannabis licensing must begin by October 1, and the emergency regulations would allow for the licensing of cultivators, product manufacturers, dispensaries, and transporters, with individuals or organizations only permitted one type of license.

Under the emergency regulations, only one dispensary would be allowed in each of the state’s 12 District Court Judicial Districts; no dispensary could be located within 1,000 feet of any school, daycare, church or hospital; at least 51% of an applicant’s business or organization must have resided in Nebraska and be a U.S. citizen for at least the past four years; and applicants would have to pay to submit two legible sets of fingerprints to the FBI and the Nebraska State Patrol for a criminal background check.

The regulations do not specify qualifying conditions for medical cannabis access but require that a physician’s recommendation specifies the product being recommended, the recommended dosage and potency, the number of doses, the directions for use, and the name of the patient.

The regulations allow dispensaries to sell oral tablets, capsules, or tinctures; non-sugarcoated gelatinous cubes, gelatinous rectangular cuboids, or lozenges in a cube or rectangular cuboid shape; topical preparations; suppositories; transdermal patches; and liquids or oils for administration using a nebulizer or inhaler. Flower is not permitted under the regulations, neither are infused food or drinks, any products containing artificial or natural flavoring or coloring, or any products that can be smoked or vaped.



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