South Carolina § 44-33-10 Sickle cell education and prevention program.

South Carolina Statutes

§ 44-33-10 — Sickle cell education and prevention program.

South Carolina·Title 44 HEALTH·Ch. 33 SICKLE CELL DISEASE

The Department of Health and Environmental Control is hereby authorized to initiate a sickle cell education and prevention program based entirely upon voluntary cooperation of the individuals involved. The program shall provide:

(1)laboratory testing of citizens in the reproductive ages to determine the presence of the sickle cell gene;

(2)counselling for persons identified as carriers of the sickle cell gene, for the purpose of educating these persons about the risk of a child of the person inheriting sickle cell disease;

(3)referral of persons with sickle cell disease, as necessary, so that they may obtain proper medical care and treatment, to include pain management; and (4) basic education to the general public about sickle cell disease, so as to eradicate the stigma attached to the

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The Department of Health and Environmental Control is hereby authorized to initiate a sickle cell education and prevention program based entirely upon voluntary cooperation of the individuals involved. The program shall provide: (1) laboratory testing of citizens in the reproductive ages to determine the presence of the sickle cell gene; (2) counselling for persons identified as carriers of the sickle cell gene, for the purpose of educating these persons about the risk of a child of the person inheriting sickle cell disease; (3) referral of persons with sickle cell disease, as necessary, so that they may obtain proper medical care and treatment, to include pain management; and (4) basic education to the general public about sickle cell disease, so as to eradicate the stigma attached to the disease.

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Legislative History

HISTORY: 1962 Code SECTION 32-562; 1972 (57) 3013; 2022 Act No. 206 (H.3166), SECTION 2, eff May 23, 2022. Effect of Amendment 2022 Act No. 206, SECTION 2, redesignated (a) to (d) as (1) to (4); in (1), substituted "citizens" for "black citizens"; in (2), substituted "educating these persons about the risk of a child of the person inheriting sickle cell disease" for "preventing sickle cell anemia in the future offspring of such carriers"; in (3), substituted "disease" for "anemia" and inserted ", to included pain management; and" at the end; in (4), substituted "the disease" for "this malady"; and made nonsubstantive changes throughout. ARTICLE 3 Sickle Cell Disease Voluntary Patient Registry Editor's Note 2022 Act No. 206, SECTION 1, provides as follows: "SECTION 1. This act may be known and cited as the 'Rena Grant Sickle Cell Disease Voluntary Patient Registry Act'."