I had my last colonoscopy a 2-3 years ago and told my GI I was having sharp stabbing pain in my left lower pelvis area. He dismissed my concerns and said it was my IBS. I told him I know I've had IBS/GERD now barretts for 30 years and know the symptons. Fast forward I struggle with IBS - C and D and and I starting having that pain more frequently. I know what to eat and what no for my issues. Recently I noticed my bowel movement were perfect balls about a little smaller than a golf ball. always about 5 at a time. Then I noticed mubowel movement looked identical like small pellets. Bouts of normal movement, constipation, severe diahreia not making it to the toilet in time or I my colon was like numb and I would have a small movenet with no feeling until i got the the bathroom. It has advanced and I changed Gi's and can't get an appt. until the end of July. A recent scan can showed diverticulousis but I know it has advanced beause I sometime see light pink tinge after I wipe. I have about 8 major autoimune illness and a ton of offspring. Lupus and Sjogrens have helped themself to all my organs and body parts literally. I feel like I'm slowly dying. Any comments, suggetions would be appreciated,. Wondering why my doctor didn't see the diverticulosis when I had the colonscopy. Is it visible? How long does it take to take from the time I started having sharp jabbing pain in my pelvis to diverticulitis. Many thanks.