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New federal rules require medical facilities to post spreadsheets itemizing their charges. Computers can read them, but people can’t.

Medical aid in dying is only an option for those with six months or less to live, but even still-healthy people may want to know how the new law could apply to them.

Milestones, a nonprofit treatment center for youth with autism, cerebral palsy and other developmental disorders, served 1,700 children since opening 10 months ago.

The program aims to provide stronger reporting on under-covered topics.

The U.S. takes forever to approve drugs before they can be sold to the public, but no such caution is taken with new devices.

Prominent Honolulu lobbyist John Radcliffe, whose colon cancer has spread, became the first state resident Wednesday to start the application process.

A Civil Beat investigation found frequent shortcomings with how Hawaii’s education department handles workers’ comp claims.

The state estimates around 40 people will use the new law to seek medical assistance to end their lives next year.

Micronesians face language and cultural barriers when seeking medical care, and are far less likely to have insurance coverage.

Big companies are self-insuring themselves and taking other steps to control medical costs. Is this a return to plantation days?