Hemophilia Assistance Plan
The purpose of this state-funded program is purchase of blood products for persons with hemophilia or other congenital blood clotting disorders.
- U.S. citizens or lawful permanent residents
- South Carolina residents
- Household income at or below 250% of the federal poverty level (pdf) or enrollment in fee for service Medicaid or contracted Medicaid programs.
- Payment for blood products prescribed for home infusion
- Care coordination and related services, as needed.
How to Apply
Contact your nearest regional CSHCN office.
Patient Services Inc. (PSI) offers assistance with cost of health insurance premiums, prescription co-pays, Medicare Part D, and other services that may be helpful to persons with hemophilia. For more information, send email to firstname.lastname@example.org or call 1 (800) 366-7741.
If you have questions about getting services for your child with special needs, please contact us.
For more information, email Children with Special Health Care Needs, call us at (803) 898-0784 or visit us at one of our statewide locations. See a brief description of the work performed by DHEC's Children/Teens with Special Health Care Needs Program.