Guest guest Posted August 24, 2008 Report Share Posted August 24, 2008 I have had AS for aproximatelly 7 years. I was first diagnosed with fibromyalgia, which may be a part of my issues, but I think most of my pain is actually from the AS.I have been through an ocean of doctors over the last 7 years, and finally found a great Rhuemy in a neighboring town. My AS has been active for the greater part of 7 years, with highs and lows/flares more common than not. I am on Lodine, sulfasalazine, tramadol, tylenol, and ocassionally on Sexlaxin.I have tried Enbrel with little sucess and am planning on starting Humira and Mobic. I am extremely worried about the side effects of these two drugs, mostly because I suffer from other autoimmune diseases which lower my immune system. However, with the current flare I am having which has lasted the last 2 months,I have become extremely tired, and the pain and inflammation are overwhelming. I have needed to take medrol dose packs 4 times in the last 2 months. I look forward to meeting others who have AS to share stories, experiences, and possible solutions. I am so happy to have found this group, and am very excited to meet you all! Jen Quote Link to comment Share on other sites More sharing options...
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