I’m 26, and I’ve had Crohn’s disease since college.
Before Crohn’s, being sick was temporary. A sore throat, a cough for a week or two, then back to school, back to work. Then a stomach ache just didn’t go away. Two weeks. Three. One month, two, three. I got worse. I was commuting an hour or more each way to college, in pain, barely sleeping, late to everything.
I needed to keep track of how I was feeling. But I didn’t have the bandwidth for a spreadsheet, a notebook, or my notes app. The best I could do was say it out loud, to my parents or to my doctor.
Saying it out loud is exactly the idea.
I still use Trace every day, and I’ve come a long way with my health. I can’t choose when a flare comes, but I’m in control of the record: the dates and details are already there for my doctor, so I’m not relying on memory.
If I found it useful, perhaps others will too. That’s why Trace is in testers’ hands now: so people who live with this every day can tell me what works, what doesn’t, and what Trace should become.



