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i just wanted to pop in here, because I forgot to last month on the five year anniversary of my colon rupturing, to say that when they tell you that the vast majority of people who have this procedure are too busy living life to come here and post, that my experience has been exactly that.

Since my horrible 2014, which began with my UC diagnosis, and quickly led to rupture, emergency removal of the colon and then a surgery to create the j-pouch, takedown and a final open surgery a couple days later because of a bleed, my new normal is pretty awesome.

i’ve traveled extensively on three continents, including a few places with general sanitation standards that should give the fully coloned pause.

I eat pretty much anything I want (except mushrooms, which I love, but which have messed me up badly a couple of times), with the knowledge that some things (I’m looking at you spicy food), will require a payment to the piper.

My professional life is strong, and the perspective gained from my experience has made me a better leader.

At almost 47 years old, I’m in the best physical shape I’ve been in since I traded high school sports for college beer.

I’ve kayaked in countless freshwater bodies, and on three different salt water seas, spent days on boats without facilities (thank you immodium), biked through vineyards in Spain, sipped champagne in the shadow of the Andes and eaten chicken mole Colorado made by an abuleta in a remote village a full day’s drive into the mountains from Oaxaca City.

Is it all easy? No. There are days when the plumbing can be challenging as hell. I’ve dealt with one bout of pretty serious pouchitis, and, yeah, I poop more than most, and gas sucks because solo farting isn’t in my skill set.

But I can’t remember the last time I counted how many times I crapped in a day. The challenges are more than manageable, I FEEL good, and most importantly, I’m not dead, and that was a very real possibility.

I recognize that for some they don’t get this outcome, and I have nothing but empathy for those who continue to suffer, but I found this forum when I was scared and alone in my fears. Much of what I found was a comfort, but I didn’t quite believe when I’d read the assurances that most people with pouches were out living their lives, happily.

Five years later, I believe.

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Your response really helps everyone here. Its been 7 months post takedown. I login almost daily here to see issues , post my own and try to know more about those who've been battling this dreadfull disease. Also I have very little to complain about. With UC life was worse than HELL. But post op I could go on trekking in just 3 months. I've done my graduation and now working in a dream job. I plan to take a trip  soon in a year. 4-5 bms a day I dont even care even when I had to go 10 times , anything for me is good as long as its painless.

As for the fitness part, I've been into workouts , yoga for a long time and having the diseases section out eased all my exercising routines. 

I know many people have issues which are bad and many others who are living a perfectly normal life. But everyone is different in his own way. They say - "Tough times dont last, but tough people do" 

Have a great day 🙌🏻

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