04/08/2026
Genetic information doesn’t end with us — but who should it be shared with, and when?
Join the Arizona Bioethics Network this April for a thought-provoking webinar exploring the ethical complexities of posthumous genetic disclosure.
Featuring Annette Mendola, PhD, HEC-C, Director of Clinical Ethics at the University of Tennessee, this session will examine the challenges of sharing (or withholding) genetic information with family members after death.
Together, we’ll explore:
• Ethical considerations around disclosure vs. confidentiality
• Current perspectives shaping this evolving issue
• Real-world barriers to communicating genetic risk
🗓 April 15, 2026
🌐 azbioethicsnetwork.org