“Congressional attention has drifted toward adult-use legalization and the chaotic hemp-derived cannabinoid market, leaving medical cannabis patients behind.”
By Steph Sherer, Americans for Safe Access
After a decade-long “ceasefire” secured through annual appropriations legislation, millions of patients and stakeholders in state medical cannabis programs now face renewed threats. President Donald Trump’s FY 2026 budget proposal reveals not only the fragility of patient protections but also exposes Congress’s failure to fulfill its promise to medical cannabis patients.
The proposal omits critical spending restrictions on the Department of Justice (DOJ) and Drug Enforcement Administration (DEA)—protections that have, since 2014, prevented federal interference in state medical cannabis programs. Without these safeguards, hard-won protections established by the Commerce, Justice, Science, and Related Agencies (CJS) Appropriations Amendment—commonly referred to as the Rohrabacher–Farr Amendment—would be dismantled.
Since its passage, this amendment has shielded patients, caregivers, state regulators and cannabis businesses from federal prosecution, arrest, asset forfeiture and harassment. It was never intended as a permanent fix, but as a temporary measure while Congress developed a national medical cannabis policy. Unfortunately, that progress has stalled. Congressional attention has drifted toward adult-use legalization and the chaotic hemp-derived cannabinoid market, leaving medical cannabis patients behind.
Sen. Barbara Mikulski (D-MD), chair of the Senate Appropriations Committee in 2014, who was responsible for ensuring that the medical cannabis protections ended up in the 2015 Budget bill signed by President Barack Obama, summed up the sentiment of that time in 2016:
In recent sessions, Congress has largely abandoned meaningful efforts to advance medical cannabis legislation. Instead, it has prioritized industry-driven bills like cannabis banking reform and broad legalization measures, neither of which is immediately politically viable nor sufficient for meeting patient needs. If medical cannabis were federally recognized, businesses serving patients would have access to banking.
While conversations around adult-use legalization should continue, they are not a substitute for the urgent need to establish a separate, comprehensive federal medical cannabis program.
More than six million Americans rely on state medical cannabis programs to treat conditions like chronic pain, epilepsy, PTSD, multiple sclerosis and chemotherapy-induced nausea. According to a 2021 JAMA Network Open study, medical cannabis laws are associated with a 23 percent reduction in opioid overdose deaths—just one example of how these programs improve health outcomes and save lives.
Without the CJS amendment or comprehensive federal legislation, medical cannabis programs remain at risk.
While the 2022 Medical Marijuana and Cannabidiol Research Expansion Act protects medical professionals, patients, caregivers and their providers face renewed threats of criminalization. Removing this amendment signals a dangerous shift away from compassion and common sense at the federal level.
Let’s be clear: The goal of the medical cannabis movement is not adult-use cannabis. Recreational markets are not designed to meet patients’ clinical needs for consistent, measurable and medically supervised cannabis therapies. State-level experiments have shown that these markets fail to deliver adequate products, pricing or protections for patients.
Efforts to protect medical cannabis access federally date back to the 1970s. In the 1980s, lawmakers like Reps. Stewart McKinney (R-CT) and Newt Gingrich (R-GA) introduced legislation to provide compassionate access for patients with life-threatening conditions. But those efforts collapsed under the renewed drug war.
In 1992, President George H.W. Bush shut down the federal Compassionate Investigational New Drug (IND) program, which had allowed a small number of patients—including glaucoma patient Robert Randall, the first to receive federally supplied cannabis—to access medical cannabis legally. Its closure left patients with nowhere to turn, sparking a grassroots movement to pass state medical cannabis laws.
Three decades later, we are still operating under a patchwork of temporary state protections. Patients in federal housing, active-duty military members, federal employees and those in federally regulated healthcare settings are barred from using cannabis. For many, traveling with or relocating for medical cannabis treatment remains legally perilous, and those who depend on Medicare or the Veterans Health Administration for healthcare can only use cannabis medicines if they can afford to pay out of pocket.
During the “ceasefire,” patient advocates have worked tirelessly to lay the groundwork for permanent federal action. In the absence of comprehensive congressional leadership, they have cleared many of the barriers that once hindered reform. This includes championing regulatory changes to enable U.S.-based research, debunking the long-discredited “gateway drug” theory and establishing safety protocols for cannabis intended for human consumption.
Advocates helped shape a marketplace capable of testing for a broad spectrum of cannabinoids and contaminants, supported the rescheduling of cannabis under United Nations treaties and collaborated with FDA to demonstrate that cannabis has “accepted medical use in treatment in the United States.”
Most significantly, they secured legal access for more than six million Americans through state-based frameworks across 40 states, the District of Columbia, and four U.S. territories.
The groundwork has been laid—now Congress must act.
Americans for Safe Access (ASA) has long advocated for permanent reform that would reclassify cannabis under a new Schedule VI and establish an Office of Medical Cannabis and Cannabinoid Control within the Department of Health and Human Services, creating a regulatory framework distinct from those used for alcohol, tobacco or conventional pharmaceuticals. Patients deserve more than workarounds—they deserve a healthcare system that can address their medical needs.
The upcoming July markup of the FY 2026 CJS Appropriations Bill is a critical opportunity. Congress must restore the CJS amendment and recommit to building a permanent, patient-centered federal program. Patients should not have to fight every year for basic protections.
Medical cannabis is not in competition with adult use, but history shows us, across the U.S. and globe, that one does not happen without the other.
It’s time for Congress to move beyond temporary measures and create lasting federal reform that will integrate medical cannabis into our health care systems. Please join us in letting Congress know this is a priority.
For more information on the past and current fight for safe access, watch this virtual town hall:
Steph Sherer is the founder and executive director of Americans for Safe Access (ASA) and the chair of the SafeAccess4All.org campaign. ASA is the largest national organization of patients, medical cannabis providers, medical professionals, scientists and concerned citizens promoting safe and legal access to cannabis for therapeutic use and research, with over 150,000 supporters in all 50 states.
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Multi-state cannabis company TerrAscend Corp. on Tuesday announced it is exiting the Michigan market, planning to sell or divest the company’s assets in the state, which include four cultivation and processing facilities, 20 retail dispensaries, and real estate.
The company plans to use proceeds from the sales to pay down existing debt.
In a statement, TerrAscend Executive Chairman Jason Wild called the decision “strategic” and said it followed “an extensive evaluation.”
“Michigan is an extremely difficult market, and we have come to the realization that our resources can be better utilized in our other markets. This move will unlock value for TerrAscend and its shareholders. By concentrating our efforts and resources in the company’s core northeastern U.S. markets – New Jersey, Maryland, Pennsylvania and Ohio – I am confident that we are now positioned to deliver stronger financial performance, including improved margins and operational efficiencies.” — Wild in a press release
The actions associated with the Michigan exit plan are expected to include a reduction of approximately 21% of the company’s overall workforce, TerrAscend said, which consists of about 1,200 employees as of June 30, 2025. Most of the reduction is expected to occur by the end of the third quarter of fiscal year 2025.
Following the completion of the plan, the company will operate 19 dispensaries and four cultivation and processing facilities across five U.S. states, including New Jersey, Maryland, Pennsylvania, Ohio and California, along with facilities in Toronto, Ontario, Canada.
The Michigan exit is expected to be mostly completed in the second half of this year and the company’s business in Michigan will be reported as discontinued operations beginning with the company’s financial results for the second quarter.
Nebraska Gov. Jim Pillen (R) on Tuesday signed emergency regulations for implementing the state’s voter-approved medical cannabis law. The regulations were approved last week by the state Medical Cannabis Commission.
The regulations allow the state to begin licensing medical cannabis cultivators, product manufacturers, dispensaries, and transporters. Under the rules, individuals or organizations are only permitted one type of license.
During a meeting last week, the commission also entered into a memorandum of agreement with the Governor’s Policy and Research Office and the Department of Health and Human Services (DHHS) to assist with legal and administrative processes during the creation of the permanent rules. The permanent rules are due October 1. Pillen said in a press release that the participation of those agencies will ensure Nebraska’s cannabis industry is properly regulated as outlined in the ballot initiatives passed by voters and signed into law.
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. Neither flower nor infused food or drinks are allowed under the regulations, and any products containing artificial or natural flavoring or coloring, or any products that can be smoked or vaped, are banned.
TG joined Ganjapreneur in 2014 as a news writer and began hosting the Ganjapreneur podcast in 2016. He is based in upstate New York, where he also teaches media studies at a local university.
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