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

Summary

The bill establishes a Rare Disease Task Force inside the Mississippi Rare Disease Advisory Council to study gaps in care, insurance coverage and funding for rare diseases, and to advise the state on solutions. It also amends a hospital‑pilot program by replacing the word “license” with “exemption” and sets rules for those exemptions. The measure is signed into law and will take effect after July 1, 2026.

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