My uro wants me to visit Dr. Payne at Stanford. Have any of our members seen him? What can I expect?
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Dr. Christoper Payne
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Hi Sharyn,
I have not seen Dr. Payne either, but I've only read wonderful things about him. He's big in the IC research community, so I suspect you'll be in good hands.
I hope one of his patients will post to you. In the mean time, you could check out a transcript from his appearance on the ICN, which discusses the use of BCG:
http://www.ic-network.com/guestlectu...payne1001.html
Good luck to you!
Melanie J."The sun shines not on us, but in us." John Muir
Living a happy life in spite of IC! http://www.ic-network.com/patientstories/melanie.html
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I read the article that was posted. I wasn't aware that he would take me as a patient. I haven't had very good luck with the last 6 so it is conforting to know that there is another doctor for me. At least my current uro was honest and referred me to Dr. Payne. I give him credit for that.
Did you participate in any experimental programs?
At times I have had some remission over the last 3 years and it was encouraging. My appt. is in Oct. so I will post the results.
Meanwhile I am on my own and value the suport of my fellow IC friends.
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Dr. Payne is absolutely wonderful. If I still lived in the Bay Area, I would definitely continue to see him. He is very compassionate and was there for me all those times when I came to his office for an appointment in tears. Due to my IC, I had to move to be with my mother for awhile. I was sad to say goodbye to Dr. Payne, as he was the first doctor (and only doctor since) that has truly listened to me, and not made me feel melodramatic. I know he's involved in lots of research studies, so in my opionion, he's the guy to see! Wish you the best of luck!
Sara
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