Hospital records tell you (but mostly clinicians/insurers) what happened in a clinic. They don't tell anyone that that prescribed antibiotic didn't work, how your mental health affected your symptoms and the timeline of how it all escalated, or that you skipped that medication because the side effects made you unable to work. They don't tell you what your baseline actually is/was, or what your symptoms look like at 3am versus 3pm, or that the dose that works for most people doesn't work for you. This is the context that only you have. What's yours? What do you know about your own health that no system has ever captured? And what would change if you could effortlessly share it with you clinician?

If you've moved countries what was your biggest health data challenge?

Here's what HDA looks like in practice. Meet Anna a real case shared by one of our early adopters, with some details adjusted for privacy. Her records span Latvia, the UK, and Spain, across three languages.
Check out the demo account to see how it looks like.

TLDR

What Health Data Avatar offers that others don't

• Unique sharing with fine-grained access controls

• Multilingual embedding (shout out to @Qwen3 )

• Multiple profiles writing access (essential for parents and other unpaid carers in real life there are usually more carers for one person, but existing tools aren't built for this reality) removed for the version we're currently launching for a smoother experience

• Removing identifiables before interacting with LLMs (or generally exposing your health records publicly)

• With all this, top security standards and privacy-first architecture (which doesn't make observability and many other things easy on top of just thinking about privacy at every step and every decision, including frontend)