Hey everyone! I was just wondering if anyone has heard any information or comments on the lupus center at Johns Hopkins. My nephrologist called me today and he and my rhematologist were talking the other day and they have decided they want me to get a second opinion with a rhematologist at Johns Hopkins. My doctors said they have tried all the cutting edge treatments with me and they feel they are not getting anywhere. I have to say I am glad to have the doctors I have. They are very supportive and determined to get me better. And they actually talk to each other and noone is in the dark about my helath situation.
If anyone has any information I'd appreciate it. If not that's okay too! Thought I'd ask! :lol: