A medical record for women who keep getting dismissed.
Janie holds what the chart leaves out.
Record your visits. Document what you asked for, what they recommended, and what you declined. Build a record you actually own, across every doctor, every diagnosis, every year.
Join the waitlistEarly access opens this fall.
Why this exists
Women managing chronic reproductive conditions see four, five, sometimes ten doctors over the years it takes to be heard. Black women take the longest to be diagnosed, are dismissed most often, and are steered toward more invasive treatments when alternatives exist. Their advocacy disappears from the chart. What they asked for, what they declined, what they were told — none of it travels with them to the next visit.
Janie is the record that does.
Record.
Tap record when your visit starts. Place your phone on the desk. Janie listens.
Remember.
Janie turns the visit into a structured record — what was recommended, what you asked for, what you declined. Verbatim quotes attached.
Return.
Walk into your next appointment with a record that travels with you. Across providers. Across years.
What you see
Your medical life, as a single document.
Recorded visits become structured entries. The doctor’s words sit in amber. Yours in green. Refusals are stamped, dated, undeniable.
Tap the play button or the three dots — see what Janie does.
Who we’re building for
Janie is built first for Black women navigating chronic reproductive conditions — fibroids, endometriosis, PMOS (formerly PCOS), chronic pelvic pain — in the United States and Canada. The product is designed for the conditions of care those women actually face: short visits, fragmented records, dismissive providers, and a system that doesn’t keep their advocacy on file.
Join the waitlist.
We’re rolling out access through fall to women in the U.S. and Canada. Tell us where you are and what you’re managing, and we’ll let you know when we open.