Hi,
I am new to the forum and glad I found it. My son, 20 has Crohns disease.
He was diagnosed with UC in his early teens and after every drug, and years of trying every med, and many flares he now has a j-pouch. The path report on the colon indicated UC. About a year after his reversal, he started having problems again. Turns out now he has Crohns and is on more drugs than ever before. Not sure how much relief he is getting from the medication. The Crohns is now in the small intestine (which was beautiful before surgery) and the small intestine is what made his j-pouch. The pouch has changed shape and is very narrow causing much concern. The docs are very perplexed. I am praying that the meds help and he can keep his pouch. He doesn't complain much of pain...let me know if any of you have experienced this....I know their is no easy answer, it's just good to find a place to go and express yourself.
Thanks for reading.
I am new to the forum and glad I found it. My son, 20 has Crohns disease.
He was diagnosed with UC in his early teens and after every drug, and years of trying every med, and many flares he now has a j-pouch. The path report on the colon indicated UC. About a year after his reversal, he started having problems again. Turns out now he has Crohns and is on more drugs than ever before. Not sure how much relief he is getting from the medication. The Crohns is now in the small intestine (which was beautiful before surgery) and the small intestine is what made his j-pouch. The pouch has changed shape and is very narrow causing much concern. The docs are very perplexed. I am praying that the meds help and he can keep his pouch. He doesn't complain much of pain...let me know if any of you have experienced this....I know their is no easy answer, it's just good to find a place to go and express yourself.
Thanks for reading.