MDA Advocacy Institute: Spotlight on Kids' Access to Care and Treatments

  Рет қаралды 45

MDA

MDA

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In this MDA Advocacy Institute, we cover updates on our plans for the last few weeks of 2024 and discuss how we’re urging Congress to finalize critical legislation for the neuromuscular disease community, including the Accelerating Kids’ Access to Care Act and the Rare Pediatric Disease Priority Review Voucher program reauthorization.

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