Google
Trusted Resources: News & Events
Latest announcements and gatherings
Coronavirus, Racial Disparity in Sickle Cell Disease
Despite being a rare condition, sickle cell disease is the most common inherited blood disorder in the US. But it does seem to affect discriminately; despite only 70,000-80,000 Americans suffering from it, sickle cell disease is diagnosed in 1 in every 500 African Americans.
This is not an uncommon circumstance in medicine. Unfortunately, neither is healthcare disparity—the wide gap of positive versus negative care outcomes that seems to split US patients by ethnicity.
In the final portion of an interview with HCPLive®, sickle cell researcher Ken Ataga, MD, of the University of Tennessee Health Science Center, discussed the plentiful work needed to be done in order to lessen the healthcare disparity gap, particularly in this disease.
+myBinderRelated Content
-
You Should Get a COVID-19 Vaccine – Spanishhttps://www.youtube.com/watch?v=awFzaU9c...
-
You Should Get a COVID-19 Vaccine – Arabichttps://www.youtube.com/watch?v=YQBfcUyB...
-
Sickle Cell Disease Association of America Extends its COVID-19 Emergency FundraiserThe Sickle Cell Disease Association of A...
-
COVID-19 and Sickle Cell Disease-Related Deaths Reported in the United StatesSickle cell disease (SCD) is associated ...
-
Coping With Anxiety & Fear From Quarantine Dr. Gayle Rogers – WebinarThe Sickle Cell Mental Health Initiative...
-
Depression & the Sickle Cell Warrior – WebinarThe Sickle Cell Mental Health Initiative...
-
MARAC Statement: Update About COVIDThe worldwide pandemic of COVID-19 (SARS...
To improve your experience on this site, we use cookies. This includes cookies essential for the basic functioning of our website, cookies for analytics purposes, and cookies enabling us to personalize site content. By clicking on 'Accept' or any content on this site, you agree that cookies can be placed. You may adjust your browser's cookie settings to suit your preferences. More Information
The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.
Powered by
Support for this site is provided by
This platform is made possible through a partnership with the Sickle Cell Disease Association of America, Inc. (SCDAA) and its member organizations. SCDAA's mission is to advocate for people affected by sickle cell conditions and empower community-based organizations to maximize quality of life and raise public consciousness while advancing the search for a universal cure.