The “Research & Policy Updates on Sickle Cell Disease” topic was originally presented during National Minority Quality Forum’s weekly webinar series. Listen now for a closer look at addressing existing disparities.
Participants:
Anjulika Chawla, MD, FAAP Medical Director in Medical Affairs and US Sickle Cell Disease lead, bluebird bio
LaTasha H. Lee, PhD, MPH Vice President, Social and Clinical Research & Development National Minority Quality Forum(Moderator)
Trending Topics
Features
- Drive Toolkit
Download and distribute powerful vaccination QI resources for your community.
- Health Champions
Sign up now to support health equity and sustainable health outcomes in your community.
- Cancer Early Detection
MCED tests use a simple blood draw to screen for many kinds of cancer at once.
- PR
FYHN is a bridge connecting health information providers to BIPOC communities in a trusted environment.
- Medicare
Discover an honest look at our Medicare system.
- Alliance for Representative Clinical Trials
ARC was launched to create a network of community clinicians to diversify and bring clinical trials to communities of color and other communities that have been underrepresented.
- Reducing Patient Risk
The single most important purpose of our healthcare system is to reduce patient risk for an acute event.
ecori
pubmed