Mucus Discharge Post-Colostomy: Seeking Advice

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phillg
Aug 25, 2015 3:49 am

I have had a colostomy for 20 years and now being bother with mucus coming from rectum. It used to stop in 3-4 days, but now it is contiues Any ideas would be appreciated.

Wilski
Aug 25, 2015 4:13 am

Try a rectal enema eg Fleet, to flush out the mucus. I've had similar experiences when I had my colostomy. 

Bill
Aug 25, 2015 9:30 am

I used to irrigate with a gadget fixed up to the shower in the bath - but that was just to get rid of the nasty, smelly stuff. After a while I only discharged a clear mucus with no odour so I stopped irrigating and use incontinence pads instead. It's all about choices!

Best wishes

Bill

Posted by: Nini4

Well,  I  hit the two year mark. I went back and read my posts from when I first found this site. I was very fortunate in that I stumbled upon it only 4 weeks post op. I have said many times that this community really saved me. The first 2 weeks after my surgery I shut down completely. It wasn't until about the 3rd week that my son came in to my room, flicked on the light and told me I was going to have to get back to living because I was scaring him. I had fallen into such a depression.  He  ticked me off,  but it also made me stop and think- what was I going to do? Feel sorry for myself and sulk, or be grateful I was alive. 

I've re-read my journals from that time and it was after my son kicked my butt, so to speak, I took an honest inventory and had to dig deeper than I've ever had to. I mean, I had survived a pretty nasty divorce, after a pretty crappy marriage and that was tough. But this was different. I felt like I was now a handicapped person who would be limited in their life and be looked at as a freak. My mental state was precarious, at best. 

But then I found this site. I just lurked a bit before posting. I read so many of the other stories and I started to see just how full my life can be, I was not handicapped,  and certainly not a freak! The stories of survival, the sense of humor, the support and compassion was inspiring.  It was then I made myself get out of the dark, and get my sh*t together.  

Not all rainbows and sunshine at first, hardly! But with grace from myself - to myself, and the kindness and willingness of the folks here to be supportive, non judgemental and openly share intimate details about their life circumstances,  l not only survived but thrived. 

I think of all the years I had suffered with such extreme pain, barely functioning,  and the many hospital stays and how that is all behind me now.  (All fingers, toes, and legs crossed that I never have to go near a hospital for myself ever again. I think I'd rather have a fork stuck in my eye. I loathe every about them.)  

So, to everyone who has been a part of this journey with me, to say thank you is not enough. I'm forever grateful to know you all.  My Angels, each one of you. 

 And as the Grateful Dead famously said,

"what a long strange trip it's been!"

Im so happy I'm tripping with you all.


B4_R2D2
Aug 26, 2015 5:41 am

The first two years of my ileostomy I retained my rectum with the hope of getting a J-pouch, and like Bill, I wore women's panty liners in my briefs.  Since my rectal sphincters were too damaged by my crohns/colitis, I opted  to have my rectum removed.  That gave me another 8 week vacation from work which saved me from a layoff period.  However, if you still have a useful rectum, I'd suggest you consider a possible option of colostomy reversing reconnection.  Why wear a pouch if you don't need to?  Or if the rectum and sphincters are't viable, maybe rectum removal.  More on rectal mucus at:  http://www.healtharticles101.com/bowel-mucus-do-i-have-problems-with-digestive-tract/  OBTW, the UOAA bi-anual 4 day educational & Fun Conference starts next Wednesday, 9/2 Even I with 27 years since my first belly surgery will be there, as I always learn something good.  

Good luck and God bless.  Bruce

B4_R2D2
Aug 26, 2015 5:44 am

PS.  check out the UOAA web site at OSTOMY.Org.  Bruce

 

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