Anyone else suffer from UTI or kidney infections? I have both an ileostomy and a urostomy, and have been having some bad infections in the past. My symptoms include nausea, fever and vomiting, my urine will look like lemon juice, or milky, or red from blood. I was hospitalised twice last year for treatment. It took my doctors 12 months, and about six infections to come up with the right medication. They are very reluctant to go straight to a permanent antibiotic, that is the last resort. A lot of time was wasted trying over the counter medicines, they would only work for a few weeks, then I would get another UTI. I had lots of urine tests to find witch bug was causing my problem. I tried cephalexin antibiotic, that worked for a short time, then another UTI. Back to the doctors, needless to say, I was getting sick and tired of the continual UTI infections. I was given another daily antibiotic, called trimethoprim, 150mg a day. It's been a few months so far things are ok. However, I'm worried what will happen when, or if this antibiotic stops working, due to the bugs getting amuned to it. My specialist tells me there are only four types of antibiotic to control UTI, and I've already tried three, including Amoxycillin. When I asked the specialist why I'm getting the infections, I was told its cause a section of intestine was used to create my ileal conduit, or urostomy, and that living piece of intestine continues to produce bacteria, going straight to my kidneys. I'm told it's unavoidable, even if I drink lots of water. So, I'm wondering does anyone else with a urostomy suffer from continual UTI or kidney infections, and if so, how do yo deal with it?
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Hi Deb,
As you can see, the outpouring of love and support from this website will help you to find the strength to lift yourself up and out of your current emotional situation. I am lucky to have my husband by my side through all of this, so I will not even pretend to know how you feel and what you're going through alone. I do know that I have great friends on this site and in my life that have been by my side, and hopefully you have many by your side as well. You do have a lot of new friends here. Please feel free to talk through anything that is on your mind. We all go through a confidence deficit when we go through an ostomy surgery. Our body has been marred and your mind feels that way sometimes too. It is tough to move on, but you will. You will be stronger once you realize that you are still the beautiful woman you were prior to your surgery. Hopefully, you can reach out to a local support group and find some additional friends in your same situation. It always helps to have a sounding board wherever you find it!
Puppyluv
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