Guest guest Posted June 14, 2005 Report Share Posted June 14, 2005 Thank you very much for the advice. > >Reply-To: >To: >Subject: chicago dr. >Date: Tue, 14 Jun 2005 10:00:20 -0700 (PDT) > I live just north of Chicago in Wilmette. I was dx with PSC in 2002, saw a doctor and Rush Hosp. and was displeased with him. I had done so much reaseach before I saw him that I pretty much know what I had and the standard urso treatment. He did prescribe urso but I asked him frankly " How many patients do you have with PSC " and he responded " Less than 10 " . I went to Mayo and was extremely pleased with their system and the Dr/NP that I saw there, Dr. Lindor and Gossard, NP. I would recommend going there for an initial work up so you can get any and all tests done in 1-2 days (and sent home with complete results). I'm going to start looking for a doctor locally for when I develop symptoms, I'll have someone close. I went to http://www.nmff.org/findphysician/physearch.asp and http://nmhphysicians.photobooks.com/list.asp?Lastname= & Specialty= & SpecialInt=1065 & Language= & Sex= & Insurance= & Keyword= & SetIndex=0 & Search.x=55 & Search.y=12 I HAVE NEVER SEEN THE ABOVE DOCTORS, but at least they put PSC as one of their areas of expertise. On a slightly different note, one of the Dr's at the conference in Denver mentioned that IU Medical Center had an extremly high rate of matching people that need transplants. Therefore, even though I've never been there, if you need to be listed, I'd meet some doctor's there too. Now I've got you driving all over the midwest, but a good PSC doctor is like life insurance, you don't want to look for one well after you need it. My 3 cents. Dike Ajiri PSC 2002 __________________________________ Yahoo! Mail Mobile Take Yahoo! Mail with you! Check email on your mobile phone. http://mobile.yahoo.com/learn/mail Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 14, 2005 Report Share Posted June 14, 2005 My family lived in Wilmette for 5 years, though they have recently moved to New York I am still a patient at the UNiversity of Chicago. I love them, THey have preformed 3 surgeries on me and i have no complaints. Dr. Tea (sp) is my hep and Dr Millis is my guy, he is the transplant surgeon and is involved in great research their. I seem to get vip treatment every time im there. IN fact i leave on monday to go back for another operation. dont realy know what else to say, so u ask anything u need to know about them. Dan 22 uc psc, so close to part 2 i can feel my 6 pack coming back __________________________________________________ Quote Link to comment Share on other sites More sharing options...
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