Health Disparities: Sickle Cell, Research and CRISPR

Health Disparities: Sickle Cell, Research and CRISPR

Date: September 27, 2018

Time: 02:30PM – 04:00PM

Where: bit.ly/VKSsicklecell

You must be registered to participate!

About 100,000 people in the United States have sickle cell disease, with most of the patient population derived from communities of African descent. While life expectancy for almost every major disease or chronic condition is improving, patients with sickle cell disease can expect to die younger than they did 20 years ago. In 1994, life expectancy for sickle cell patients was 42 for men and 48 for women. By 2005, life expectancy had dipped to 38 for men and 42 for women.

Gene editing offers the potential to find therapies for life-threatening and/or debilitating human genetic diseases – from cardiac and metabolic diseases, to neurological diseases such as Huntington’s disease, to sickle cell anemia. Yet human gene editing raises many questions related to bioethics and equity.

This session centers on the intersection of scientific research and public policy to eliminate health disparities, we will seek to answer:

• Why we are moving in the wrong direction in terms of life expectancy?
• What are the barriers to care?
• Who can access these therapies?
• How is personal choice given a fair voice?
• Who funds a cure?

Keystone Symposia is striving to advance understanding and elimination of persistent health disparities in the United States by incorporating discussion into our conferences on cardiovascular and metabolic diseases, immunology, cancer, and other diseases that impact populations worldwide.

Building on the previous Keystone Symposia roundtable conversations on Health Disparities: The Intersection of Science and Race and Health Disparities: Type 2 Diabetes, Research and Policy, this session centers on the intersection of scientific research, sickle cell and CRISPR in the effort to address health and health equity.

Event Hashtag: #VKSsicklecell