Having a rare disorder, I’ll take “any doc who’s actually heard of the damn thing”.
Support group online is chock full of people who went to an ER with what I have and were mistreated for days until someone found a neurologist with a clue.
I stumbled into not one, but two docs (one male, one female), WELL versed in my disorder at the specialty level. For the GP, I stumbled into the PA (female but it didn’t matter) who was described by colleagues as “if you have something strange going on, if anyone around here will figure it out, she will...”.
The PA left the State. A recent follow up to the family clinic she worked at had me on the schedule of the doc who started the place. He’s not accepting new patients, he just keeps a few slots open to cover patient visits. After a 30 minute straight talk about my “stuff” he walked to the desk and told the nurse not to assign me to another doc, he would keep me. He also prescribed a drug even the neuro hadn’t heard of which has completely dealt with one of the side effects of my condition. Even got the neuro curious.
Also had an ER doc recently who took time to listen and understood when certain questions were asked, my honest answer had to be “I don’t know.” (She asked about gut pain. I can’t tell you for sure if I can even feel the stuff right now. Maybe, maybe not. Because with nerve issues going on, there’s no way to tell if those ones are working properly or not. I know for sure I can’t feel my shins, for example, but guts? No idea.) I’m sure after we talked she went and looked up my thing. Ha. But she took the time and got the reason I was there.
So yeah. I’ll go with “knows what they’re doing and listens” even if they haven’t heard about my specific rare thing. And I’ll go out of my way for “has even heard of the disorder”. And I’ll travel states for “knows proper treatment for the disorder without being prompted.”
They teach docs to not see zebras instead of horses. Unfortunately I’m a zebra now.