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I’m curious how others approach disclosing diagnoses to clients when a diagnosis isn’t required for insurance, meds, or external documentation. Do you: 👉Always share the diagnosis? 👉Share it collaboratively only if it feels clinically useful? 👉Hold off unless the client asks? 👉Frame symptoms/patterns without naming a diagnosis? One piece I’m actively wrestling with is whether sharing a diagnosis can sometimes create a self-fulfilling prophecy—where clients begin to identify with or even manifest symptoms they hadn’t experienced prior to being informed, especially with highly descriptive or stigmatized diagnoses. I’m holding this alongside values of transparency, client autonomy, empowerment, and neurodiversity-affirming care—and wondering when a label supports growth vs. when it subtly narrows self-concept. Would love to hear how others think about this ethically and clinically, what you’ve observed in practice, and how this plays out across different populations (teens, ND clients, trauma histories, etc.). No right answers—genuinely curious about collective wisdom. 💬✨