My GI dr. prescribed me
hydrocortisone enemas and uceris for flare-ups after my colonoscopy in November. They
found some polyps, thankfully the results came back benign. However, they also found
some abnormal cells; which means I have to go back every 3 months for a colonoscopy until they can
figure out what's going on. I'm currently in the middle of a flare-up, and I'm
a little afraid to try the enema. I've never used them before, and I was told
there is a burning, stinging, and sometimes painful sensation when using the
enema. I was also told there are horrible side effects to it.
Can anyone that have used or is using
hydrocort enemas shed some light for me please?
Post Edited (angee23) : 1/10/2014 8:15:14 PM (GMT-7)