The Health Resources and Services Administration (HRSA), part of the U.S. Department of Health and Human Services, is asking the public for feedback on their Sickle Cell Disease (SCD) programs. These programs aim to improve the care and outcomes for people with SCD, a group of blood disorders that mainly affect Black and Hispanic Americans. The HRSA funds several initiatives to increase awareness, provide better care, and connect those affected with community resources. Public comments will help shape future programs to better support people with SCD and their families. Comments must be submitted by January 6, 2025.
Simple Explanation
The HRSA wants people to share their ideas on how to help those affected by Sickle Cell Disease, which is a blood problem mostly affecting Black and Hispanic people. They will use these ideas to make their programs better so more people can get good help.