Your Data.
Your Decision.

• Easier for individuals to be empowered and engaged in decisions;
• Easier for providers, social service agencies, and community-based organizations to coordinate care for vulnerable populations;
• Easier for emergency responders to know an individual’s treatment and care plan for end-of-life care;
• Easier for researchers to identify and communicate with clinical trial participants;
• Easier for providers to collect feedback on patient satisfaction and outcomes after receiving care;
• And easier to build trust with clients and patients by giving them more control over their personal data, and more reasons to feel confident about how their data will be shared and used.

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