Thank you for visiting the ICN Support Forum. We are so happy that you found us! The ICN Support Forum is home to 50,000 patients who have participated in our 24/7 support system. However, to protect the privacy of our members, members of the public can not read posts unless you have registered first.
It's easy to register! Just click the "sign up" button in the upper right corner of the page. Make sure you use a correct email address because we'll send you an email to confirm that you are a real person!! We also screen all new applicants to verify that they aren't bots or spammers! If you have any problems, please feel free to send a quick email to: [email protected]!
I had that test done and it was called an ultrasound. It's uncomfortable for everyone because you have to drink and fill the bladder and hold it. That was early on in my trying to "diagnose the problem" era. I also had a test where I had to pee into a special potty that was hooked up to a computer measuring what came out and the human tester was sitting right there. I could hardly let anything out,just from the embarassment of it. I'm not sure what that test was called.
Neither of the tests were painful.
Nottoc - I'm sorry, I didn't see your message before. At any rate, that sounds pretty much like the test I had to take, but I got a little privacy during my urination and I was so ready to go anyway that it wasn't difficult. Though it was uncomfortable - perhaps because I had a UTI as well.
Thanks MG. When I used to get cathed, I only had to hold them 1 hour but I would try for 90 mins or 2 hours just to really get the best benefit. I was shocked when I was told this new protocol is 4 hours. No way. 3 hours is SOOO difficult, especially in the middle of the day. I even get up for breakfast and don't drink water or milk or tea or anything - just sips for toothbrushing and pill-taking. Still can't make it.
I do think it is helping and I do hope this UTI was sort of a one time thing. I seem to get them about once every year or two these days - 15-20 years ago it was 4-6 a year. I still have it hard-wired into my brain about all the things to avoid a UTI, including jumping up right after being intimate and using the bathroom. I used to think it had something to do with my partners because I have been married twice and had a couple of relationships where I seemed to get many more UTIs, but now that I look back at it, I realize that the relationships with higher incidence of UTIs were also much more stressful relationships, and maybe were IC flares, instead. Funny how we're wired, isn't it?
I wouldn't worry too much about getting more UTI's, yes you may get more they probably won't be a problem for you if you have been being cathed for a while and not gotten them it proablay was just from being run down post surgery, or you picked it up during surgery and it just brewed along for a while till something made the bacteria start getting to be more.
I could not hold for more than 1 hour I am sure so I think it is great you can do 3 hours.
I have low immunity, I don't get instils because of getting UTI's, I only get cathed when absolutely necessary. I usually can't pee for days after being cathed I am sure just from the irriation and my ureathra swelling, this cause's the urine to sit in my bladder too long and hence the UTI.
Although the last few times I have had to be cathed, it has been at my own clinic and they listen to me that I want the lidocaine gel and a small cath, this has helpped a lot I can pee after if they use a small Cath, and I ice afterwards.
When I think I have a UTI ussally nothing shows up in the dip because of my immunity problems, I always get a culture. My Dr. sometimes gets me to start Ab's before the culture, but he always does a blood test and if my WBC count is up then he starts me on ab's and a temp.
In your case you recently had a cath, and surgery, I too would be skeptical of UTI without symptoms and no bacteria, I often get blood in my urine without a UTI, with IC our bladders can bleed, some Dr.'s don't understand IC enough to know this does not mean the same thing as someone with a normal bladder.
Hope you are feeling better MG
Wow, MG, I'm sorry to hear about how that is not an option for you. Doesn't everything have to be complicated? Sigh.
I have been getting cathed for most of the last year on a fairly regular basis and this is the first time I have had a UTI - also discovered after the second instill cath from this doctor's nurse, who uses the small ones and yes, plenty of lidocaine. I almost don't feel them at all. I'm still skeptical.
Thing is, this doc is listed with the ICA as being an IC specialist and he seems to know more about it than my original gyne does, who was the one giving me the instills for most of the last year. He, in fact, trained my other gyne on how to do it, etc. The only difference is that he and his nurse want me to "hold it" for 4 hours whereas my other gyne only required 1 hour. I haven't made it past 3 yet - 4 hours is DIFFICULT to say the least.
I am really impressed with his knowledge otherwise, but can't figure out why this was diagnosed as such. However, I think they were correct, because shortly after I started taking the antibiotics, my bladder stopped being so achy/sore as it had been for about a week before that. I hadn't specifically noticed because of the recent hysterectomy, and had blamed that.
Oh well, either way, I'm done with my antibiotics and back to instills, though I have to admit I'm a bit concerned I'll get another UTI now, because I know you can get them so easily from caths and this is a different doctor. Hmm.
I know I went to the urology department up at the Medical College of Georgia. OK. The doctor that I had was an older dude that said he had retired once and that it was his last week before going elsewhere. Geez! Regardless, he did state the interstim would not be a good idea with my back being messed up. OK. He did state he wants for me to have urodynamics assessment. That is scheduled to be done on August 10, but I guess I won't be seeing him ever again.
I have low immunity, I don't get instils because of getting UTI's, I only get cathed when absolutely necessary. I usually can't pee for days after being cathed I am sure just from the irriation and my ureathra swelling, this cause's the urine to sit in my bladder too long and hence the UTI.
Although the last few times I have had to be cathed, it has been at my own clinic and they listen to me that I want the lidocaine gel and a small cath, this has helpped a lot I can pee after if they use a small Cath, and I ice afterwards.
When I think I have a UTI ussally nothing shows up in the dip because of my immunity problems, I always get a culture. My Dr. sometimes gets me to start Ab's before the culture, but he always does a blood test and if my WBC count is up then he starts me on ab's and a temp.
In your case you recently had a cath, and surgery, I too would be skeptical of UTI without symptoms and no bacteria, I often get blood in my urine without a UTI, with IC our bladders can bleed, some Dr.'s don't understand IC enough to know this does not mean the same thing as someone with a normal bladder.
Getting the uti really could be from any number of things.
I get one just about everytime I get cathed.
You should start to get over it pretty quick after starting the ab's.
Feel better soon MG
Wow - I'm sorry - I have to tell you if I got a UTI nearly every time I got cathed, I wouldn't go with the treatment. This is only my first post-cath - I've had 30-35 instillations and I would be antibiotic-intolerant if I had one each time. I'm sooo sorry that happens!
I'm really curious about the fact that they told me it was a UTI based on leucocytes and blood in urine which is common in IC patients, but they didn't culture it to see if there was bacteria. I showed an old urinalysis to my other doctor who diagnosed me, and it said "too numerous to count" WBCs, moderate epithelial cells, and no bacteria, and she told me that wasn't a UTI. I didn't have any UTI symptoms at the time, either. So I guess I am skeptical now of being diagnosed with UTIs, especially when I think that it's possible all the diagnoses of UTIs I had in my early 20s and antibiotics may have something to do with my developing IC. I just find the whole thing confusing.
That is what i kind of figured the bladder scan was, I didn't know they would measure as you peed.
Glad it went well for you, sorry you have a UTI, but better to know and be able to get it treated and to feel better, 4 weeks after a hysto is early, it takes at least 6 weeks for things to bounce back to normal.
I had 2 booked one day after the other in mid Aug. but I had to change the dates so now they will be in mid Sept. oh well.
Take care MG
Thanks, Mothergoose. I'm bummed about the instill because they help so much. And then I'm also nervous that maybe the instill led to the UTI because I haven't had a UTI in a couple of years, and this is my first one since I've been getting instills from the new doctor. But really, it's probably just so many dang things going on at once in my body, plus my family is having crazy issues (health), and life goes on, y'know?
Take care and I hope you're able to get one moved back to Aug.
That is what i kind of figured the bladder scan was, I didn't know they would measure as you peed.
Glad it went well for you, sorry you have a UTI, but better to know and be able to get it treated and to feel better, 4 weeks after a hysto is early, it takes at least 6 weeks for things to bounce back to normal.
I had 2 booked one day after the other in mid Aug. but I had to change the dates so now they will be in mid Sept. oh well.
OK - it turned out to be really simple -
- go in with full bladder
- they put an ultrasound wand on my bladder to measure the size (took 2-3 seconds)
- I urinated in a funnel which went into a beaker on a weight or scale that had leads to a computer that read volume, velocity, if I dribbled or had a full solid stream, etc
- after, they wanded my bladder area again to make sure it was empty or if any was left
And that was it.
Though 3 hours later they called me to tell me I had a UTI And as a result of that I can't have my Elmiron instill tomorrow. Bum out. But maybe part of why I'm still so sore from my hysterectomy which was performed 4 weeks ago tomorrow. Hopefully I'll be feeling better soon.
I had that test done and it was called an ultrasound. It's uncomfortable for everyone because you have to drink and fill the bladder and hold it. That was early on in my trying to "diagnose the problem" era. I also had a test where I had to pee into a special potty that was hooked up to a computer measuring what came out and the human tester was sitting right there. I could hardly let anything out,just from the embarassment of it. I'm not sure what that test was called.
Neither of the tests were painful.
So I asked the nurse today what the bladder scan entails - it doesn't sound that bad. What they do is I go in with some urine in my bladder, they run a probe over my bladder to see how full it is, etc, then they have me urinate in a special toilet that measures how long it takes me to urinate, when I have the strongest stream, etc, sort of like a graph of my urine flow. Then once done, they re-scan my bladder with the wand to see if I got it all out. It takes about 15 minutes, no sedation, no real pain other than what I normally feel when I urinate lately. So that is a huge relief!
Thanks Mothergoose. I have had an ultrasound with this doctor before and he doesn't believe in, as he put it, "tormenting IC patients" by making them do the full bladder ultrasound thing. He also didn't call it an ultrasound. Either way, I guess I'll find out when I ask tomorrow after my instillation. At least I will have had a treatment only 2 days before.
Thanks and I'll be sure to explain later what the "bladder scan" turns out to be.
Leave a comment: