The risks of misinformation being spread through online patient forums can be mitigated by communication strategies aimed at physicians and organizations.

Equal access is a goal even when patients present with taboo illnesses. But, the date of a patient’s last drink still matters.

Would you question health decisions made by a 37-year old Black woman whose great-grandfather died in the US Public Health Service Syphilis Study at Tuskegee?

Felix Gonzalez-Torres' and Gregg Bordowitz’s works express their experiences of living through a pandemic and subsequent social change and draw out key human rights themes.

Transitions in relabeling personalized medicine as precision medicine, precision health, or wellness genomics reflect shifting the locus of responsibility for health from individuals to clinicians and in shifting focus from genetic risk to genetic enhancement.

Focusing on social processes contributing to marginalization can help clinicians and policy makers mitigate food insecurity risk through improved patient-centered care.

Using crowdsourced information in health professions education can help motivate critical appraisal, question asking, and evidence evaluation skill development, especially among “digital natives.”

Current QoL conversations in HTx could be enhanced by a phenomenological account of temporality, embodiment, and intersubjectivity.

Ethical and practical problems with preference modeling can undermine how reliably predictors can be used in high-stakes decisions.

Reliance on disclosure rather than understanding has prompted shared decision making and represents an important cultural change in clinical practice.