Good morning. I was diagnosed in 2007 with UC. 2009-2010 was when I had the surgeries for the j-pouch. Have been battling with issues pretty much since then. In 2014 I was told I had Crohn's. Cimzia did nothing for me. I'm now on Methotrexate and Entyvio. These are not working either. Gastro doctor recommends having pouch removed. He sent me to the Mayo for a 2nd opinion. They claim it's not Crohn's but possibly Pelvic Floor Dysfunction? The pouch is good but not functioning properly. I have the constant urge to have bowel movements, lots of painful cramping, nighttime accidents and peri-anal sores and discomfort.
Mayo does not want to continue with my care and referred me back to my gastro doctor who believes I'm in remission for the Crohn's. He's ordering an anorectal manometry to check my pelvic floor muscles. Based on that outcome, he believes I should go to the Clevelend Clinic to see the #1 expert in the nation on pouches.
Right now I'm angry, frustrated, confused and just plain sick and tired of all the non-help I'm getting.
Is there anyone who's gone through this or something similar. I really do not know what to do.
Thank you,
Patti