Sickle cell disease association of America, Inc. awards community based organizations with $2,033,080 for newborn screening follow-up program | oneSCDvoice
  • Join Today!

Become a member and connect with:

  • An Active Online Community
  • Articles and Advice on SCD
  • Help Understanding Clinical Trials

Sickle cell disease association of America, Inc. awards community based organizations with $2,033,080 for newborn screening follow-up program


The Sickle Cell Disease Association of America, Inc. (SCDAA) was awarded $2.9 million annually for the next four years from the Health Resources & Services Administration (HRSA) for the Sickle Cell Disease Newborn Screening Follow-up Program in June 2017. With these funds, SCDAA is continuing its efforts to establish the national infrastructure to ensure that individuals diagnosed with sickle cell disease (SCD) receive appropriate care coordination and follow-up services including counselling, education materials and access to a medical home.

SCDAA has identified 16 community based organizations (CBOs) in fifteen states, to receive $2,033,080, 70% of its 2017 HRSA grant award, to support them with the capacity to identify, educate and link patients to care in 15 states across America.

https://www.onescdvoice.com/wp-content/uploads/2018/02/SCDAA.jpg