Hi everyone,
I'm 25 as of now and in november of last year, I had an episode of rectal bleeding. It lasted about three days and freaked me out really bad. I thought it might be cancer but when it remained stopped, I attributed it to possible hemorrhoids and moved on.
Two months ago, I started noticing that my stool was either mushy or finger thin. But I was going to the toilet only once a day like I always have. I was also bloated most of the day, especially after meals. So I finally decided to see my GP last week. He booked me for a colonoscopy the next day. During the test, he said he found moderate to severe inflammation throughout my colon with erosions in my rectum and sigmoid colon. Multiple biopsies were taken as well. I was heart-broken when I learnt I probably had UC and would require lifelong treatment.
Interestingly,the biopsy report was mostly normal except for detecting some chronic inflammation in the superficial layer. I've attached the picture of the report. It says "no features of IBD seen" yet my doctor still thinks it's UC and has begun me on two pills of mesalazine for life.
Should I get a second opinion? Considering I haven't had the classic symptoms of UC like recurring blood in stool and strong urgency for toilet trips. I'm lost and don't wanna be treated for something I don't have.