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New Sickle Cell Treatment Centers: Better, Coordinated Lifelong Healthcare Access

This law establishes a nationwide network of specialized Sickle Cell Disease Treatment Centers using a "hub-and-spoke" model. The goal is to ensure patients have access to coordinated, comprehensive medical care throughout their lives, including advanced therapies and social support. Citizens affected by this disease will gain better access to specialists, assistance with insurance, and help addressing daily challenges like transportation or food insecurity.
Key points
Creation of "hub-and-spoke" networks to deliver comprehensive care, including stem cell transplants and gene therapies, led by specialized medical centers.
Implementation of programs to improve the transition of patients from pediatric to adult care, ensuring continuity of treatment.
Funding for assistance with accessing health insurance, social services, genetic counseling, and transportation for patients.
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Additional Information
Sickle Cell Disease Treatment Centers Act of 2024
Print number: S 5226
Sponsor: Sen. Van Hollen, Chris [D-MD]
Process start date: 2024-09-25