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For health systems & vendors

Informed patients are
better for everyone.

I ♥ Data is a partner to health systems. When patients understand their rights and take an active role in their care, outcomes improve, trust deepens, and the entire system works better.

32%
Reduction in readmissions among highly engaged patients
$1M
Maximum fine per violation of the Information Blocking Rule
40%
Of patients say data transparency would increase trust in their provider
2x
More likely to follow treatment plans when patients understand their diagnosis
The business case

Why I ♥ Data is good for health systems & vendors

Patient empowerment is a competitive advantage, a compliance asset, and a care quality driver.

Better clinical outcomes
Patients who understand their diagnoses and have access to their records are more likely to adhere to treatment plans, catch errors before they escalate, and engage meaningfully with their care teams.
Reduced compliance risk
The 21st Century Cures Act and HIPAA carry significant enforcement teeth. Organizations that proactively support patient data access face far lower risk of information blocking complaints and OCR investigations.
Deeper patient trust & loyalty
Patients increasingly choose providers based on transparency. Organizations that make data access easy differentiate themselves in a competitive market. Trust is a retention strategy.
Fewer disputes & grievances
Many patient complaints stem from feeling uninformed or denied access. When patients feel empowered rather than excluded, dispute rates drop. Transparency is a de-escalator.
Interoperability & data flow
Organizations that embrace Direct Secure Messaging are better positioned for the interoperable future of healthcare — and reduce the burden of records requests on their own staff.
Equity & community trust
Historically underserved communities often have the lowest rates of patient portal use — not from lack of interest, but lack of awareness. I ♥ Data's community-first approach helps close that gap.
Partnership opportunities

How we work with health systems & vendors

We're here to help you build something better with your patients and communities. Click each to learn more.

We co-develop plain-language patient education materials — for waiting rooms, patient portals, discharge packets, and community outreach — that help your patients understand their data rights and exercise them through your systems specifically. Co-branded, culturally appropriate, and designed to reduce burden on your staff.
Front-desk staff, care coordinators, and clinical teams are the first line of contact when patients ask about their data. We offer training workshops — in person or virtual — to help your team respond accurately, confidently, and in the spirit of transparency.
We partner with health systems on community events, health fairs, and outreach campaigns that educate underserved populations about their data rights. Co-branded materials and joint programming demonstrate your organization's commitment to transparency and equity.
Our team brings deep expertise in patient data rights, HIPAA, the 21st Century Cures Act, and Direct Secure Messaging. We work with health IT teams, compliance officers, and patient experience leaders to identify gaps and design patient-centered data access workflows.
For EHR vendors, health information exchanges, and health IT companies — we offer co-development of patient-facing features, joint advocacy for stronger interoperability standards, and market positioning support around transparency and trust.
Get in touch

Let's talk about partnering

Whether you're a hospital system, health IT vendor, payer, or community health organization — we'd love to explore what working together could look like.

Transparency is the future of healthcare.

Let's build it together.

About our team Patient rights guide