u/AcanthaceaeGold8738

Hey everyone, I'm planning to build a migraine tracker, but before I go all-in on development, I want to get a neurologist's perspective first.

I know tracker apps have mixed reviews some genuinely useful, some not and I'd rather hear from the people actually treating patients than guess at what works. A few things I'd love to understand:

• How much time do you realistically have to review patient-tracked data?
• What kind of data actually helps you make treatment decisions, and how much is enough?
• And some more questions....

My goal right now is to genuinely talk to and empathize with both sides patients and doctors and then build a solution that actually helps both.

If you're a neurologist (or work closely with one) and open to a quick 20–30 min chat, I'd really appreciate it. Happy to work around your schedule.