▲ 7 r/lupus
New Englanders with lupus, what's your experience?
I hope I'm allowed to ask this question here due to how specific it is, so apologies in advance if not.
I'm considering moving from FL to somewhere in New England (not sure exactly where) due to unbearable sun/heat and the drs here aren't as knowledgeable about my disease(s) as I'd like.
I've heard the hospitals in New England are better. Has this been your experience? I currently have income-based charity care here, where if I go to the monopoly hospital chain, whatever my insurance doesn't cover is covered by the hospital's charity care. Google says they have something like that in Mass. Has anyone experienced this?
And overall, how has your experience with lupus been living in the New England area? Are the doctors good?
u/Ashamed-South-7361 — 2 days ago