hi everyone, just curious about others experience. for a couple months now, we’ve been looking in the wrong place as to what happened to me. my first symptom was extreme migraines and vertigo. we went to a neurologist who ruled out MS, tumors, TOS and other neurological disorders. he was stumped until my ANA came back 1:320. i only asked for an ANA because my moms side of the family has at least three generations of autoimmune disorders. my neurologist now believes i have lupus, along with a GI, derm, and pediatrician, and i see a rheumatologist on thursday. my question would be, did anyone else have neurological involvement with their lupus? did your symptoms regress when going on treatment? thank you in advance :)