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 ($57,625 for family of four) or current Medicaid coverage.
- 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
or call us at (803) 898-0784.