If every time I see you we discuss how I have Systemic JIA/Still’s, why do y’all have me listed as having polyarticular? My SJIA is definitely polyarticular in nature, but um…
Do y’all not listen at all to your patient? And to the (limited) records? And symptoms?
I just, um…
I hope I really like this new rheumy I’ll be seeing because I honestly don’t want to go back to this office.
Before I got more into the empowered patient movement, I would probably have let this slide, but honestly not cool.
My previous rheumatologist to these guys put many things in my record inaccurately.
Does anyone know what to do to remedy all this?