I've done some research on bowel obstruction for crohn's, I only have crohn's in the small not large bowel. From the syptoms I've read it's sounds like I may have one. But I was hoping someone who has had this problem could give me their story and how it felt.
Every 2 months after starting remicade(done remi,on humira as of 2 weeks ago) I will end up in the hospital, from something I ate, triggers the suppose ulcer (scope 5 years ago said ulcer,but god knows what it could be now) and I throw up for hours before saying time for hospital visit. Before remicade it would be 3 visit's a week. In recent visits blood test are saying it's not a flar. But all the syptoms are CD. For the rest of the 2 months I have these awful pains (not like usual, same pain just different) always bloated, more gassy then usual. I'm hardly eating so it's not the food,when I do eat, it could take a few painful hours for the food to go down with nausea. Usual ending in having to take a gravol then just crash out.
Does any of this sound like a partial blockage? or maybe an ulcer that isn't crohn's related? CD in small bowl,stomach, colon. (from last scope done a little over 5 years ago) next one is end of sept. and my doctor never returns her message, so no way of getting ahold of her.
Thanks for any help in advance.
25 year old woman. Crohn's all my life but diagnosed at age 18.Been on prednisone 8 times. which they will not give me anymore(doesn't work for me)I am on Prevacide for the ulcers I get in the stomach,pantesa. I've been on and off imuran,entocort,number of others I can think of. I have cronh's in the small bowel,colon,stomach. Since Nov 08 I've been suffering from RA which is just as bad as CD. haven't been able to work for the last 2 years. Awaiting to start Humira since being on Remicade for 1 year 4 months that no longer works.Now on Humira and back on Imuran as well.RA pains all gone!