Has anyone been to HSS in NYC to their lupus center? I’m going to call this morning to see if I can get an appointment. I want another opinion on my dx and my treatment. I’ve been in a flare on and off for over a year. I’m so tired of feeling horrible.
Judging by their website, Jend, it certainly looks like HSS is knowledgeable about lupus and could offer a valuable second opinion. I don't know any other members who have been there, but I hope someone will chime in. If you do make a visit, please report back on your experience there. I hope you feel better soon!
I someone chimes in also. I called their lupus center n gave a short version if my story and she said I should be seen and would reach out to their dr’s for the next available appointment. Then she called back asking about the insurance. So I’m waiting for a call back from someone regarding that … Ugh