explores the role of the law in improving the health status of people-of-color and to assure access to quality health care.
Institute on Race, Health Care and the Law
Related posts
Personhood, When Convenient?
In early August, an Alaska woman named McKenna West was serving as a gestational surrogate for a Los Angeles couple when a prenatal diagnosis revealed the fetus had hypoplastic left heart syndrome, a serious but treatable congenital heart defect. According to West’s own account, the intended parents asked her to terminate the pregnancy. She refused […]
In The News…A Surrogate, Parents, and Politics: Clearing up the Ethics of Surrogacy Disputes
This essay is a part of our “In the News…” series, where bioethicists give their take on popular news stories. A gestational surrogate “fleeing” from Alaska to Texas is getting a lot of press. The issues around this story may not be that new, but rather reflect the precarious situation between legal surrogate contracts and the […]
Whose Values Define Value? Procedural Justice and the Personal Utility of Clinical Genomic Testing
This editorial appears in the May Issue of the American Journal of Bioethics The recent increases in the number of persons detained by ICE in the United States is affecting health care. Many health-care professionals and facilities that serve immigrant communities report a chilling Health Technology Assessment (HTA), and the value assessment frameworks that underlie […]
Evaluating the Price of Oregon’s Psilocybin Services: Finding the Right Comparison
Oregon’s psilocybin services are often described as quite expensive in both media coverage and academic discussions. However, when making this claim, we should ask: expensive compared to what? Whether or not psilocybin services are considered too expensive may, in fact, depend in large part on whether their use is being thought of as healthcare, a luxury experience, a quasi-therapeutic […]