EM secondary to Lupus


Is there anybody out there with EM secondary to Lupus-am wondering if this is me and would to share/compare!


I meet criteria for Lupus and have been put on plaquinqel a year ago, now cellcept and steroids. I have damage to my autonomic nervouse system from it. I started with the burning feet and hands last year mainly with my flares and when they treat me with steroids and cellcept it gets better. All that is left for now is mild burning but summer is coming. Tylenol and elevation and cool rooms help.