Rare Disease Task Force; establish within the Mississippi Rare Disease Advisory Council.

Summary

The bill establishes a seven‑member Rare Disease Task Force inside the Mississippi Rare Disease Advisory Council. It will study gaps in care, review insurance and funding practices, and issue annual recommendations to state leaders. The goal is to make rare‑disease treatments more timely, fair and affordable for Mississippians.

AI-generated summary — may be incomplete or inaccurate. Verify against the official bill text.

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