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built for the diagnostic odyssey

A simple app for medically complex people.

Mine brings your medical research together in one place, so you can uncover patterns, connect the dots, and find answers faster.

Join the beta No iPhone? Prefer desktop? Open mine in your browser.
01

enduring a diagnostic odyssey

Is its own special kind of hell. Navigating a siloed medical system, waiting months to see specialists, and astronomical medical costs, all while being treated as an unreliable witness to what's happening in your own body.

Mine is the first platform that's always relevant and always up-to-date, because it's managed by the person most invested in your health — you.

02

organized research

No more phones full of context-less screen shots. Explore quality research for yourself or someone you care for; then save, organize, and share it. Knowledge is power.

Review · J Am Coll Cardiol, 2019
Postural Orthostatic Tachycardia Syndrome: JACC Focus Seminar.
Postural orthostatic tachycardia syndrome (POTS), the most common form of orthostatic intolerance in young people, affects approximately 500,000 people in the United States alone, typically young women at the peak of their education and the beginning of their working lives. This is a heterogeneous disorder, the pathophysiology and mechanisms of which are not well understood.
POTSOrthostatic IntoleranceDysautonomia
Study · Psychiatry Res, 2019
Do different factors influence whether girls versus boys meet ADHD diagnostic criteria? Sex differences among children with high ADHD symptoms.
We investigate if different factors influence whether girls versus boys meet diagnostic criteria for attention-deficit/hyperactivity disorder (ADHD) among children with high ADHD symptoms. Participants were 283 children aged 7-12 from a population-based study.
ADHDGender DifferencesParents
03

family accounts

It's hard enough to take care of yourself when you feel terrible, let alone everyone else.

Mine allows you to create separate spaces for each person: your parent, your child, yourself, or anyone else you care for. Family accounts keep everyone's research in its own place and allow you to switch between them in one tap (without big tech mining your medical info).

04

flexible daily log

Log daily symptoms, triggers, or whatever is most important to you. Visualize your flares on a calendar heat map.

For someone with a rare disease, the average diagnostic delay is over five years.

Children and their families wait even longer, typically six to eight years.

05

appointment prep

Now you can be organized and prepared without giving off hypochondriac vibes (lugging around that giant binder). Centralize all of your data points and visualize changes over time. Easily share them with your doctor and reference them against your research.

oh, and in case no one else has told you…

you're not crazy.

it's not in your head.

your experience is valid.

you deserve answers.

Join the beta