MI SB0610

Requires the Michigan Department of Health to establish and maintain an electronic database tracking uterine fibroid incidence, prevalence, demographic data of diagnosed women, and treatment options used by health professionals

Mandates health professionals who diagnose or treat uterine fibroids to submit data to the database in a form specified by department rules, with patient identifying information kept confidential

Requires the department to begin publishing annual summary reports of the collected data within 2 years of the law taking effect, with subsequent reports due within 180 days after each calendar year ends

Directs the department to develop and disseminate educational materials about uterine fibroids, including information on racial/ethnic groups at elevated risk and treatment options beyond hysterectomy

Requires the department to partner with nonprofit organizations and higher education institutions to implement a public awareness campaign about uterine fibroids, associated risks, and FDA-approved treatment alternatives to hysterectomy