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Hi I'm new to this group. I was diagnosed with UC in 2002 and took all kinds of prescriptions, then went years without treatment due to lack of insurance, then got back into treatment in 2017. By then the doctors couldn't decide if I had UC or Chron's. I've been on all kinds of biologics now, with no improvement. I've developed dysplasia all throughout my colon, all precancerous. After my last colonoscopy, my gastroenterologist decided that I need to have a 2 stage J pouch surgery. I've had my surgery consultation, and will have an ileostomy on Jan 7th.

I'm very scared. I'm scared of the surgery, the recovery, and the bags and probably the pouch later. I've been reading that leaks are very common and I should expect to have to get up a few times during the night. My surgeon says I'll need to drink electrolytes and take probiotics, but didn't get more specific. I'm worried about the cost of that, and wondering what other supplies I'll need post surgery.

I'd really appreciate any advice or reassurance you can offer. My family has been here for me, but there aren't any ostomates or people with pouches that I know, so I've been feeling pretty alone.

Tags: Upcoming, scared, surgery

Replies sorted oldest to newest

Hi,

stress makes everything worse. Stay positive, you seem like you have a good support system with your family. You will do fine, the ileostomy is only temporary until you heal and then get the J pouch. I’m 43 years into this, I had the two step Procedure twice six years apart. yes the beginning was tough, But with medication you can control the leaks, Until your body gets used to everything and you should fine. we are here for you.,Sending prayers!

Y

Hey! I am sorry that you need surgery and I am sorry for your suffering. The best advice I can offer is to have faith everything will be okay. Faith and Hope are what got me through the dark times, I hope Faith and Hope can do the same for you. I have made a couple posts of ostomy care that I think will help you. You can message me anytime you need support and I will do my best to be there for you.

God Bless.

https://www.j-pouch.org/topic/...ions-and-anti-fungal

https://www.j-pouch.org/topic/...y-care-that-i-follow

M

Of course you are absolutely terrified.  This is a huge life changing event.  Give yourself the grace to know it is a big change but having read what you have already been through hopefully this is a means to an end.

My ileostomy was the result of emergency surgery so I had very little time to prepare.  I was given lots of support in the hospital by the ostomy nurses and I went to some ostomate meetings where I met with other people who had ostomies for a variety of reasons.  I believe that was the most helpful because...they didn't look any different or act differently.  They lead full and interesting lives and were full of joy and knowledge.  I also went down the Youtube rabbit hole and watched all kinds of influencers who live with ostomies.  They were full of encouragement.  I also learned many tips and tricks for bag changes and clothing choices via YouTube.

My ileostomy and eventual J-Pouch gave me my life back.  I am so very happy I had it done and have had very few issues.  Sure there is trial and error with the odd leak but you learn to roll with it, learn preventative tips, and always have extra supplies with you.  I continue to work as a nurse, I have been a long haul flight attendant and enjoy competitive highland dancing.

Take a deep breath, arm yourself with solid, up to date knowledge, go to ostomy group meetings, know there are millions of people living productive and healthy lives with ostomies and j-pouches.

Good luck.

J
@Jen H posted:

Thanks so much. I really appreciate the kind words. This has been so overwhelming. I try to find as much info as I can and get overloaded/intimidated. I've been trying to find in person support groups near me, but haven't found any yet.

Your welcome. Here is a link to try to find a support group. I used this link and found so much support https://www.crohnscolitisfound...find-a-support-group

https://www.mycrohnsandcolitisteam.com/

M
Last edited by Mary2017

Don’t be scared. I know that’s easy to say but I’ve been through it, many people have. I have had my “temp ileostomy” since 2016. I’m just now going in the spring to have my pouch surgery with Dr Remzi. Only thing stopping me was fear. The bag saved my life… I was eat up w cancer… rectal & colon. You gotta stay strong, and learn with each day. It will be good days, bad days, crying days, and days u forget “you’re not normal” … that’s being said leaks do happen , but once you find your right fit with supply’s leaks will prob be very rare. Your sleeping pattern will change, and a lot depends on what you eat to be honest. Supply cost outside of insurance can range. You can almost always find what you’re looking for online for lower cost. I find probiotic yogurt or smoothies always help. Drink plenty of fluids. I avoided soda the first 6 months due to bloating & such. Feel free to reach out if you need to chat, but please don’t be scared… you got this! I promise!

M

Don’t be scared. I know that’s easy to say but I’ve been through it, many people have. I have had my “temp ileostomy” since 2016. I’m just now going in the spring to have my pouch surgery with Dr Remzi. Only thing stopping me was fear. The bag saved my life… I was eat up w cancer… rectal & colon. You gotta stay strong, and learn with each day. It will be good days, bad days, crying days, and days u forget “you’re not normal” … that’s being said leaks do happen , but once you find your right fit with supply’s leaks will prob be very rare. Your sleeping pattern will change, and a lot depends on what you eat to be honest. Supply cost outside of insurance can range. You can almost always find what you’re looking for online for lower cost. I find probiotic yogurt or smoothies always help. Drink plenty of fluids. I avoided soda the first 6 months due to bloating & such. Feel free to reach out if you need to chat, but please don’t be scared… you got this! I promise!

Since you have a temp ileostomy, do you mean you are going to have your reconnection surgery in the spring?

M
Last edited by Mary2017

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