Start with the conversation.
Our planned experience starts with patient- or authorized-caregiver-controlled recording, with appropriate permissions before a conversation is captured.
We’re building a simpler way for patients and the people they love to understand care conversations. Less medical jargon. More clarity about what comes next.
In development. Built around patients and families.
The team plans to check your blood count again tomorrow and see how you’re feeling before deciding on the next steps.
Fictional example • Not medical adviceA conversation can happen in minutes. Making sense of it can take much longer. We’re developing a way to help bridge that gap.
Our planned experience starts with patient- or authorized-caregiver-controlled recording, with appropriate permissions before a conversation is captured.
We’re exploring AI-assisted transcription and plain-language summaries to help explain what was discussed and the next steps the care team described.
The goal: share clear updates with selected family members, so being away from the bedside doesn’t have to mean being out of the loop.
Privacy and patient control are priorities guiding development from the start.
Recording workflows are being designed around consent and appropriate authorization.
We’re designing sharing controls around the people a patient chooses to keep informed.
Summaries are intended to help people ask better questions, not replace the care team’s guidance.
When my mother was battling breast cancer that had spread to her lung, I was working full-time while trying to stay informed about her care.
I’m a nurse practitioner. But in those moments, I was also a daughter wondering what the care team had said, what had changed, and what would happen next.
That experience is why I’m building N•KNOVA: to help patients and families feel more informed, more connected, and better prepared for the conversations that matter.
Not yet. N•KNOVA is in early development. The example on this page illustrates the vision; it is not a live clinical product. We’re learning from patients, families, and healthcare professionals as we shape the experience.
Hospitalized patients and the family members or trusted people they choose to keep informed, especially those who can’t always be at the bedside.
No. The goal is to make care conversations easier to understand and revisit. Any summary should be checked with the care team when something is unclear, and it should never be used to change treatment independently.
We’d love to hear from patients, family caregivers, healthcare professionals, technical collaborators, and potential advisors. Connect with Jimarie on LinkedIn to start a conversation. Please do not send private medical information.
Have a perspective to share? Building in healthcare? Let’s talk about making care easier to understand.
Connect with JimarieOpens LinkedIn · Please don’t share private medical information.