Struggling with Recovery and Sleep After Takedown Surgery

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Recover18
Nov 29, 2018 12:53 pm

I have uc and had my takedown surgery last December, things went pretty good , I was 78kg before the surgery which is a good weight for me but I can’t get near that now. I’m still up 5 times per night and leakage every night. Which lately seems to have gotten worse and I’m feeling really run down and currently not eating now. Well once a day.  I don’t know if it’s a mental thing but I’ve no energy and no desire to eat.   I think it’s the up all night which is discouraging me from eating. I take Imodium but has no effect.   Any else struggle at night? Or any similar experience?  

 

Bill
Nov 30, 2018 6:58 am

Hello Recover18. Sorry to hear of your problems. In the early days, I used to suffer problems at night time but these gradually settled and I mostly sleep through nowadays with perhaps getting up once or twice. There were several things I did which helped in this regard. First, I got a bed that raises at both ends and forms a hammock-shape. This helps me to keep still and the device therefore stays on much better. Second, I wear a belt on the device which helps keep it in place. Third, I use a medical adhesive spray, rather than relying on the adhesive wafers. this has a much stronger bonding than the manufacturer's devices. Fourth, I am very careful when getting out of bed because that is the time when the device is most likely to break free.

I don't put on a lot of weight ( or lose it other than during operations) so I approach that sort of problem on a long-term basis and eat just a little more regularly each day if I want to gain weight. Sometimes I have food supplements in liquid form because I find that they are more easily digested than actual food.

I hope this is helpful to you  

Posted by: Audrey Warren

This site is a godsend. As a newbie (colostomy on Nov 8, '21), I look at it every day for a number of reasons. Reading what people are going through makes me grateful that my elective surgery because of a severe case of IBS-C is nothing compared to what they have been through and are still living with.

I don't have to go to the hospital for anything related to my ostomy. I feel sorry for those who do and am in awe of those who can use humor to describe their ordeal. I identify with those who express their fears. I especially identify with those who are depressed because I am clinically depressed and have general anxiety disorder. How ironic that having a colostomy eliminated some of the depression and anxiety that the IBS created. I've been widowed twice and I'm on match.com.
I immediately included my operation in my profile and am pleased to say it doesn't seem to make a difference.

And there is much humor on this site and it's one of the reasons I enjoy it so much.

I could name numerous things I've learned from reading people's comments/questions/answers.

After months following on a daily basis, my only negative comment is I don't like listing the most popular members.
It's not that I don't like these people; I do. It's that I think it elicits some "Facebook"-like banter or comments that are gratuitous.

I don't do any social media and think that its merits are overshadowed by too much negativity.

Meetanostomate is in no way negative. I just think the gallery of "popularity" detracts from what is an excellent website that deals with a serious issue that causes a myriad of emotions.

Mrs.A
Dec 16, 2018 1:33 am

Wow, it sounds like a year is quite a long time for recovery. Have you spoken to your doctor, has he/she ran any test? I am not a canidate for a reversal so I am no expert but I sure hope things get better for you.

Don't settle for what your going through, talk to your doctor.