Legal Implications & SCD

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Participants:

• Host
  • Mary Alcocer, MSc – Compassionate Program Manager, Cayenne Wellness Center
• Speaker
  • Art Grant- Attorney 

This course provides a comprehensive overview of the legal rights and responsibilities of caregivers supporting individuals living with sickle cell disease. Through expert guidance and real-world examples, participants learn how to navigate critical legal processes such as obtaining a durable power of attorney, advocating for patient rights in hospital settings, and understanding caregiver authority as children transition into adulthood.

The seminar explores how caregivers can effectively interact with healthcare systems, including knowing when and how to document patient requests, understanding hospital protocols, and requesting the appropriate standard of care. The session also delves into complex family law considerations, including child custody challenges, the role of legal documentation, and how medical social worker insights can influence court decisions.

A dynamic Q&A segment allows caregivers to raise specific concerns, seek clarification on legal procedures, and gain actionable strategies for navigating both the healthcare and legal systems. By the end of this module, learners will be equipped with the knowledge needed to advocate confidently, protect patient rights, and make informed decisions that support the well-being of sickle cell warriors.