Young cancer survivors describe cannabis access and care gaps
Cannabis Use Among US Young Adult Cancer Survivors: Impacts of Legal Context, Information Sources, and Interactions with Healthcare Providers.
AI Summary
This qualitative study examined how medical cannabis use is shaped by laws, information sources, and healthcare interactions among 23 US young adult cancer survivors aged 18–39 who reported using cannabis in the past month. Interviews conducted in 2025 explored cannabis access, communication with providers, symptoms or conditions participants sought to manage, and their views of cannabis compared with other options. The study did not include a comparison group or test a treatment intervention.
Participants described state legal status as either facilitating or restricting access to medical cannabis. They commonly relied on dispensaries, social networks, and their own research or experimentation for information. Experiences with healthcare providers varied, including limited discussion, provider hesitancy, supportive conversations, contradictory information, and concerns about stigma; many participants wanted more shared decision-making. The abstract reports perceived usefulness for managing symptoms, but provides no quantitative estimate of effectiveness. As an interview-based study of a selected group of young adult cancer survivors who already used cannabis, it cannot establish that cannabis caused symptom improvements, determine which symptoms respond best, or represent all cancer survivors. This is an abstract-based summary, not a full-text review.
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