Care kits · in pilot
Get a care kit
A care kit puts one person’s medical story in one place, out of their own records and in their own words, on their own phone: the next visit and the questions for it, one sheet to hand each clinician, what was said in the room, and who keeps the list.
What it is
Three clinicians, or seven, each holding one part. Letters that arrive after the appointment they were about. A tablet one clinic started that the other clinic is now asking about. Somebody in the family keeping the whole of it in their head, or in a tin, and answering the same questions from memory at every visit.
A kit is the pages that hold it instead. Built for one person from their own records and their own words, handed over with a passphrase, theirs to keep. It runs on a phone, it works with no signal, and nothing typed into it leaves the browser unless they press send.
Whether this is you
- More than two clinicians who have never been in a room together.
- Somebody carrying the appointments, the medicines and the phone calls, and not sleeping much.
- A visit coming up that matters, and no one place that says what happened at the last one.
Any of those, and the form below is where to start.
See one before you decide anything
The demonstration kit is built for an invented person, Marguerite, 76, so the shape can be shown without showing anyone’s record. Every name, date, medicine and reading in it was made up. Four taps is enough to see what a family gets.
The door
Five questions, and none of them ask for anything medical. The story belongs in the conversation that follows, not in a form. It goes to my email and to the website’s own form store, nowhere else, and it commits you to nothing.
I work with families in Oregon and Washington.
What happens after you press send
- I read it and write back. If a kit is the wrong thing for the person you are describing, I say so, and that costs nothing.
- The intake, at your table or on a call. An hour and a half, their records and their words. Nothing is recorded unless everyone in the room has agreed to it.
- I build it. The records gathered and read, the pages built with my own tools, and every page read back against the record it came from before anything is handed over.
- Handover, with the passphrase. One round of edits, and you run it from there. You choose what each reader sees: the family, a friend, each clinician, each with their own word.
Every kit starts with a written agreement: what I do, what I do not, what is stored where, and how you have all of it back.
Who does what
I am a care systems liaison: I work on the records and the questions, and your clinicians do the medicine. No diagnosis, no treatment advice, no medicine changes. I do not call your clinicians or sit in your appointments; the kit is built so that you do.
I work for the person the kit is about, not for a hospital, an insurer or a practice.
Written with AI, and read against the records. The pages are drafted and drawn with AI tools from the records they cite and the person’s own words. Every page is then read against those records by the person who made it. The records themselves can be wrong or out of date, and only the person’s own clinicians can tell you if they are; check anything that matters with them before acting on it. Nothing in a kit is medical advice, and nothing in it decides anything.
Before anything of yours goes to an AI tool, names, dates of birth, addresses, phone numbers and record numbers are taken out on my own machine and put back only in what comes home.
The demonstration kit, end to end: demo-today.html. What a kit costs and what else I do: the consulting page.