J-pouch Life

Hey Readers!
We have a long comment from Cynthia C. and she has a handful of really great questions for the jpouch community. Would you take a few minutes to read her post and see her questions at the end.
Thanks so much!
Megan & Mark
# Cynthia C. Cynthia C. says: February 23rd, 2010 at 11:52 [...]

My name is Sara Randall, I’ll be 25 years old next month, and I have been living with an illeostomy bag since September 9, 2009. Obviously my story doesn’t start there. When I was in high school I was energetic, super athletic, always on the go, and to self conscious for my own good. When i first [...]

Hi I’m Jackie. I’m a 25 year old woman child from my native of Michigan. I have a bit of an interesting UC story so bear with me while I get my intro out of the way. I was officially diagnosed with UC in May of 2009, but had symptoms for easily [...]

I don’t want to steal thunder from Lizz’s post below. Nay, instead she actually inspired me to post my update. I would just do this as comment for her post but I don’t know how to add pictures as a comment.
November 11th will be my 6 month anniversary of the first surgery and well, it’s [...]

There’s that great line in the bible (or the Byrds song, whichever you prefer), “a time to weep and a time to laugh, a time to mourn and a time to dance.”
Prior to my diagnosis of UC and, subsequently, Crohn’s, I was a devoted and passionate dancer.  It was my “thing.”  It was also one [...]

So, at every previous job since I’ve had IBD I’ve been very vocal about my disease.  It was practical because I was sick at the time, and when people asked me questions, the advocate in me burst forth!  Since I’ve been in remission and managed to get a job in Portland, OR in this crazy [...]

Hey Readers,
We just got this email from Tom, and he is new to seeking online support to figure out the complication he is dealing with.  Could you all take a peak at his concern and see if you have any insight.  Also, we encourage our readers to post their questions/concerns at jpouch.org because that is [...]

After I had Step Two of my three surgeries, I was expelling waste rather quickly. Too quickly, it seemed. I was afraid I couldn’t adsorb anything so my surgeon recommended chewable vitamins. Although they seem childish, you can absorb them better because you’ve chewed them first!
Even now, after takedown, I still take 2 chewable vitamins [...]

I just wanted to make a quick note about Prednisone, as many people with UC (and many other diseases) end up taking it. Back when UC was a very minor part of my life, my biggest fear (because surgery didn’t even seem like a possibility) was having to take Prednisone. I try to [...]