Hey I am looking for a dr in Seattle that is especailly good with IC any suggestions are great!
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Looking for a good Dr. in Seattle Washington
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Hi, I do not know personally of any doc in Seattle, but how about the University of Washington may have a doc there who is knowledgeable. I know if I had not been diagnosed, there was mention of me being sent there to find out what was going on. Hope you find a doc, let us know how you get on, hugs Iris. hiToday and every day you are loved, so don't be anxious about tomorrow, God will take care of you tomorrow; Live one day at a time.
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Hey Kristan,
I just sent you a private message.
Good luck..
Hugs..AngieDo the hokey pokey and you turn yourself around..that's what it's all about..whoooo!
While we have the gift of life,
it seems to me the only tragedy
is to allow part of us to die --
whether it is our spirit,
our creativity,
or our glorious uniqueness.
Gilda Radner
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The U is good - Jane Miller and the nurse practiioner who is easier to get to see. But I'm in s. Seattle so I see Emily Bradley at Minopr and James. She also works more north. She doesn't know a lot about IC but she is ameniable to trying therapies I hear about. PVI got IC in 1970! I was not diagnosed until 1991. I've tried many drugs and therapies but I tend to only resort to drugs when in a flare because when I am not in a flare (from being good on diet), I suffer only from small bladder volume (like about 7 ozs.) and peeing will relieve the discomfort. When I am feeling relatively normal, I say to myself I am glad I am not on a drug. When I am in a flare, I say, why am I not on a drug! I've recently have been trying to solve my connective issue problems in general. I look to diet and herbs mostly unless it gets really bad. I still think there is great hope for each individual finding a path to healing and there are many.
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