Posted 6/25/2014 2:35 AM (GMT 0)
I've managed my minor case of UC for 15 years. I've averaged 1-2 flares a year lasting 4-7 weeks long.
So, what has changed? My 12 year old daughter diagnosed with UC after hospitalization in Oct. 2013. Both her and I had a pretty serious flare over the summer of 2013. (First one that ever had me waking up at night.) I then, after talking with her doctors realized the obvious. I did not have IBS that my PCP and I chalked my symptoms up to be.
Fast forward to March of 2014... Had my first colonoscopy that returned a diagnosis of UC. Not flaring at the time but from all the years of inflammation my colon is damaged and full of psuedopolyps. I started Lialda 2.4 mg a day April 1, 2014. Still have some bleeding and mucus almost daily so starting Uceris tomorrow.
Finally my issue. I now have to go for colonoscopy every two years screening for CRC. First sign of dysplasia and it will mean a colectomy! This is stressing me out. I feel as if its not a matter if, but when my colon is removed. I am 41 years old and in great shape physically. I now live with a cloud of dread over me. I am your typical Type A personality so, almost a day doesn't go by without me reading/researching. UC now has completely taken over my life (and my precious daughter.) By the way she's doing awesome on remilcade!
Any advice?