J-pouch Life

It’s been two years since my takedown and, as a society, we still don’t have flying cars or cloned dinosaurs. That I know of. I mean, I check the news daily to see if any of these scientific breakthroughs have become reality, but no. Nothing. Come 2034, I better have robot legs with jet thrusters. [...]

Yup, its true, my “foster” bag wants a permanent home, it wants to be adopted. It seems like its doing everything it can to make a lovely home on my belly. Here’s the scoop. The last time I blogged I was getting ready to have the first leak fixed back in February. I went into [...]

Some humor for all of you today. If you can’t laugh because it hurts too much from surgery or a flare – I’ve been there. If you can laugh, good for you! It takes a long time to “get over” the psychological ramifications of having one of the basic human functions completely effed with. Here [...]

Hey All, I’m FINALLY home! I had to get readmitted for pain control, you can check out the whole story at my other blog, www.bloodpooptears.wordpress.com. But I wanted to let you all know that I took some pictures, they are kinda graphic as usual. So if you want to check em out…here they are. Surgery [...]

Dear fellow Jpouch.net readers, hello and how are you? I know you don’t know my full story and I apologize. It’s mainly because I’m too lazy to type it all up that you haven’t seen a complete posting from me. If you’ve stuck around long enough, you’ve seen my hernia (which is still there), you [...]

I love the logo for Jackie’s new blog! If you have a minute, go check out her posts, and hopefully she won’t be a stranger around these parts. Check our her blog here.

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 started [...]

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 10 years. In [...]

I think we’ve all been at points of struggle with these diseases where we felt hopeless. For most of us, the J Pouch operation gives us our lives back. It gives us an opportunity to live it. It gives us an opportunity to hope. I have done volunteer work for the Crohn’s and Colitis Foundation [...]