Sickle cell community leaders gather annually to convene the General Assembly of Patients, Caregivers, and Community-Based Organizations to identify and develop national community priorities; host expert advocacy and capacity-building training workshops; and provide medical, research, and legislative updates to leaders in the sickle cell space.

$450,000 Award from Chan Zuckerberg Initiative is Part of Rare As One Project Investing $13.5 Million to Drive Progress Against Rare Diseases

Nevada Physician and Medical Professor Argues Against Current Trend

ICBioethics has embarked on several activities to show the relationship between ethics and patient safety to healthcare workers, to administrators, and to patients during Patient Safety Awareness Week.

Speakers and Attendees Looking Forward to Networking Opportunities at Upcoming Conference

Evidence-Based Advocacy, International Advocacy Relations Among New Topics to be Addressed