Google
Trusted Resources: News & Events
Latest announcements and gatherings
CDC Expands SCD Data Collection Program to 7 More US States in Effort to Improve Services
The Centers for Disease Control and Prevention (CDC) will share an award total of nearly $1.2 million with institutions in seven U.S. states, allowing them to take part in a data gathering program on sickle cell disease and how it affects daily life.
The funding brings to nine the number of states in the CDC’s Sickle Cell Data Collection program. The new states join Georgia and California as CDC partners in efforts to gain population-based, comprehensive health information. The program is aimed at better understanding the needs of sickle cell disease (SCD) patients, and in developing therapies more suited to their needs and providing greater support.
“HHS is committed to normalizing the lives of people living with sickle cell within 10 years,” Brett Giroir, MD, assistant secretary for health at the Department of Health and Human Services, which includes the CDC, said in a news release.
+myBinderRelated Content
-
Uganda-American Sickle CellThe Uganda -American Sickle Cell Rescue ...
-
Sickle Cell Society IrelandSickle Cell Society Ireland (SCSI) is th...
-
Today’s Faces of Sickle Cell Disease: Beverley Francis-GibsonBeverley Francis-Gibson is a President a...
-
Raising Hope International FriendsRaising Hope International Friends is an...
-
28-Year-old Sickle Cell Survivor Becomes Medical DoctorA 28-year-old sickle cell anaemia surviv...
-
Camp JubileeCamp Jubliee's mission is to provide a w...
-
@juliemakaniScientist|Doctor - Sickle Cell Disease f...
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
SomeBodyToTalkTo connects people affected by rare diseases with trusted resources, supportive communities, and opportunities to share their experiences.