The Rare Disease Diversity Coalition’s Jenifer Waldrop shares her insider strategies on advancing health equity for rare diseases through advocacy, partnerships, and policy change.
All tagged policy
The Rare Disease Diversity Coalition’s Jenifer Waldrop shares her insider strategies on advancing health equity for rare diseases through advocacy, partnerships, and policy change.
Bioethicist Dr. Madison Kilbride sheds light on controversial ethical issues surrounding genetic testing through this interview led by Sarah Lawrence student Shaun Miller.