Hello,
I'm looking for Feed Back from anyone who has had a Bladder to Colon Fistula.
What were your Symptoms prior to being diagnosed with one?
How was it diagnosed? MRI or CT scan I'm guessing.
How was it Treated or Corrected?
How was the Recovery? (Length of time, Limitations)
Was Crohns Decease a factor in it Developing or Something else?
If Crohns Decease was diagnosed, How was it Treated?
Has it Changed how you have to live post treatment
Fistula?
Started by
KK*
, Feb 02 2012 06:16 AM
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