Patient, activist, and lobbyist, Miss Stewart uses her experience as a patient to serve as a public policy advocate for chronic pain patients. She has an unusually high success rate in enacting legislation at the state and federal level. Recently she advocated for patient centric policies at the CDC.
To learn more about her work, please see the following link.
She can be found on twitter at following link.
Health systems are increasingly deploying ambient artificial intelligence tools that listen to clinical encounters and automatically generate draft visit notes. These systems are intended to reduce documentation burden and allow clinicians to focus more directly on patient interaction. At the same time, they raise unresolved questions about patient consent, data handling, factual accuracy, and legal responsibility for machine‑generated records. Recent policy discussions and legal actions suggest that adoption is moving faster than formal oversight frameworks. The practical clinical question is...
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