Guest guest Posted September 14, 2007 Report Share Posted September 14, 2007 Hi all, this is my first post in this group! I'm so glad that there's a group out there for people with PSC or those that are close to someone with this mystifying disease. My husband (who is only 22) was diagnosed with UC and PSC this past March. Needless to say, it is devastating to find out that the person that you've been married to for only less than a year already has discovered that they have two fairly serious diseases. We are anxious to move forward with his treatment (currently he's on Urso and Asacol), and we would like to know if anyone has recommendations for specialists in the Midwest. Currenly we have heard good things about the University of Chicago, but we are looking for other options to explore too. We live in Lansing, Michigan. Thanks for any insight! Quote Link to comment Share on other sites More sharing options...
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