Since I had my urostomy almost four years ago, the amount of mucus has increased dramatically. Sometimes it is so thick that it blocks the tube to the night bag. I drink plenty of water each day, but it makes no difference. I have asked the stoma nurses if there is anything I should be doing to decrease the mucus, but they don't know.
Over the years, I have learned more from this site than from the hospital on how to deal with my ostomy. Has anyone experienced this problem and found a way to lessen the mucus, or have I just got an overexcited stoma?
Once again, your help and advice would be very welcome.
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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.
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Learn about convexity and 4 myths surrounding it.
Learn about convexity and 4 myths surrounding it.
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Hollister
Living with an ostomy doesn’t mean you have to live with stoma fluid leakage or skin irritation.
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Learn how convex skin barriers work and what benefits they offer.


