Hi,
My name is Chris and I am a 61 year old women. Last April I was diagnosed with Anklyosing Spondalitis (AS) which is an auto-immune arthritis disease. In July of last year I went to the ER as I was vomiting, had a fever and had bloody diarrhea with severe abdominal pain. Spent 3 days in the hospital. Doctors were not sure if there was a correlation at the time.
11 days ago I had the same symptoms but much worse so took myself to the ER again. A CT scan and a colonoscopy was done and I have now been diagnosed with Crohns. It is not unusual for AS & Crohns to be linked together.
I have been on Humira and Enbrel for my AS and am now going to be switched to Remicade to treat both. I am presently on Entocort and Asacol.
I have absolutely no idea what started this last flare up and still have diarrhea. How long before I should expect a normal stool if ever? How do you know if a flare is coming? Is there anything I can do to try and keep them at bay?
I am on a low residue diet and have finally started eating food after 10 days of clear liquids in the hospital. Any suggestions as to what foods are good to start off with? Today I had toast and chicen noodle soup with Ginger Ale.
I need to go back to work ASAP and I am resting for the weekend and hope to go back Monday. I feel really wiped out but I expect that is from being in the hospital for 10 days and not getting any substantial nutrition.
Any suggestions and guidance is greatly appreciated.
My name is Chris and I am a 61 year old women. Last April I was diagnosed with Anklyosing Spondalitis (AS) which is an auto-immune arthritis disease. In July of last year I went to the ER as I was vomiting, had a fever and had bloody diarrhea with severe abdominal pain. Spent 3 days in the hospital. Doctors were not sure if there was a correlation at the time.
11 days ago I had the same symptoms but much worse so took myself to the ER again. A CT scan and a colonoscopy was done and I have now been diagnosed with Crohns. It is not unusual for AS & Crohns to be linked together.
I have been on Humira and Enbrel for my AS and am now going to be switched to Remicade to treat both. I am presently on Entocort and Asacol.
I have absolutely no idea what started this last flare up and still have diarrhea. How long before I should expect a normal stool if ever? How do you know if a flare is coming? Is there anything I can do to try and keep them at bay?
I am on a low residue diet and have finally started eating food after 10 days of clear liquids in the hospital. Any suggestions as to what foods are good to start off with? Today I had toast and chicen noodle soup with Ginger Ale.
I need to go back to work ASAP and I am resting for the weekend and hope to go back Monday. I feel really wiped out but I expect that is from being in the hospital for 10 days and not getting any substantial nutrition.
Any suggestions and guidance is greatly appreciated.