Designation of people with intellectual and developmental disabilities as a medically underserved population would not solve problems of access to care.

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

This month on Ethics Talk, Dr Sheryl Fleisch discusses strategies for delivering health services to people experiencing homelessness, including street psychiatry.

After the Indiana HIV outbreak in 2015, Congress partially repealed the ban on needle exchange programs, providing funding for operations but not syringes.

Clinicians must express humility, understand local culture, collaborate, and develop an insider’s perspective on past and present life.

This commentary explores legal, ethical, and practical considerations for pharmacists and prescribers working together to address uncertainty in drug prescribing.

Physicians must resist judging the quality of life of their patients with Down syndrome and learn to listen and see them as individual personalities.

To make good communication choices for their children who are deaf or hard of hearing, hearing parents must develop their understanding of hearing loss.

Defining typical appearance as a goal of health service provision is harmful and unnecessary for traits that are stigmatized but neither harmful nor distressing.

If the safe-and-effective standard for judging devices’ potential as therapy or enhancement is inadequate, one might wonder whether BCI regulation should be overseen by the FDA.