Help needed!

Posted , 9 users are following.

I was told 18 months ago that I was suffering from LS, a diagnosis made from symptoms and the fact those symptoms improved after using the prescribed Trimovate. I've had outbreaks over this time but nothing too concerning.

However, about 4 weeks ago I had my very first urinary tract infection and took antibiotics which seemed to do the trick. However the familiar symptoms of urgency in passing urine, pain and all the usual symptoms of a UTI have been recurring and lasting anywhere from 5 to 24 hours and then going away. Tests show that there is no infection and when I asked if it could be the LS giving me the symptoms was told this was unlikely.

Have others experienced symptoms like a UTI which have been caused by their LS?

Need to get to the bottom of this as it's getting to me now.

Thanks!

0 likes, 12 replies

12 Replies

  • Posted

    Hi Suecon,

    Yes, I sometimes get the feeling I'm coming down with a UTI, similar symptoms to you. I get a pressure in my bladder feeling, discomfort, sometimes burning when I urinate.

    I avoid putting creams anywhere near my urethra. And if I use an oil as a moisturiser, I avoid my urethra then as well. Remember that UTIs are common in women anyway, but I think the LS, the creams, the irritation of the skin etc probably gives us an increased chance of getting UTIs.

    I take showers rather than baths as well, all the usual stuff to avoid UTIs. I don't even have sex anymore.

    I did some research about UTIs and LS and I found from reseach articles that LS folk are more likely to have bladder issues. But see what the others on here say, it might be more unusual than I think.

    Oh and by the way. I had my first UTI about two years ago/18 months ago. It took 3 months for the symptoms to heal fully. My bladder feels different since then and I still get sensations of discomfort if I eat certain things, ketchup is the worst! If I eat ketchup I'll have UTI feelings for about a week. I think sometimes the bladder gets irritated or sensitive.

    In terms of medical intervention... I have no idea what a doctor would suggest. Perhaps further investigation, perhaps "it's one of those things". I'm sure there are ways to keep your bladder happy though. I know certain foods can trigger discomfort.

    Hope all that was helpful!

    • Posted

      Thank you...your comments are reassuring.

      I was coming round to thinking about certain food and drinks being a trigger. Just a case now of working out what makes my symptoms worse.

      Many thanks again.

    • Posted

      You may also want to use warm water rinse when you urinate. It helps. I'm following this thread as I have same problems. For me I think it is becoming coffee as my trigger for UTI. I have to drink tons of water to counter the coffee irritation.

  • Posted

    Hi Suecon, Are you certain it is LS. 3 or 4 lady doctors at my practice diagnosed LS and I had constant UTI's with negative results. I was sent to see a gaenocologist 2 weeks ago and told it was severe Vaginal Atrophy. I'm now back on my hrt and bladder has already settled back down and getting back to normal. For me it was an estrogen defiency which I always suspected but no-one would listen. Hope you get a proper diagnosis and an end to the suffering

    • Posted

      linda, I don't think any of this is black or white. Women can have the same symptoms yet respond differently to what the docs prescribe. I have AV (didn't use hormone cream 3 years ago when diagnosed due to family history of breast cancer). Thought I could just age naturally as I had no symptoms.

      Have now been diagnosed with LS. New gyn says the lack of estrogen caused it. I have no urinary tract problems, but clearly many women here suffer from them. One will get relief from one treatment others from something else. Doesn't seem to be any consistency. But at menopause (20 years ago) I did have estrogen levels tested (were normal) so I'm not sure why your docs didn't do the same. 

      There is a woman(Shirley) who posts here. She was suffering terribly with UI issues and was finally helped by Trimethoprim for bladder infection. Seems to have been her miracle cure. I believe she has started a new thread, though I haven't been able to find it. She is about to have a cystoscopy because of bladder numbness.

      There seems to be no end to the problems some women develop. It's good to know we aren't crazy or hypochondriacs and that we may possibly be helped by reading what worked for someone else. 

      I now have fleeting BV that I can't get rid of. Again doc blames inconsistent estrogen levels that affect PH which then causes BV. Wild goose chase.

  • Posted

    Hello Sue

    I have been experiencing UTIs for longer than I have been diagnosed with LS which was in 2013.

    I had about a year or so of getting them every few months - 2 in about 3 months on one occasion.

    But in between times I had bother like yourself, as if I had an infection but the result came back negative.

    I was referred to a urologist who diagnosed me with Urethral Syndrome which does cause symptoms like this.

    I read up a lot on this syndrome and now manage it very carefully and find I get less bother than I did.

    I was given the option of a camera in my urethra to check for issues but due to the LS I was not keen as it would also mean having an anaesthetic to avoid pain and distress due to the LS.

    So far I feel I am managing it a lot better than I did.

    I suggest you go back to your GP and tell them how much bother it is giving you aside from the infections and perhaps get a referral for further investigation.

    I did also get a bladder scan which came back clear.

    It is a very, very distressing condition on top of LS and possibly caused by it as confirmed by my urologist.

    Wishing you all the best.

    Persist and get some help for sure.

  • Posted

    Oh yes! For months I thought I had or was getti g a UTI, all my over the counter tests strips were negative. I also had stress incontinence ( squirted whenever I sneezed, coughed, jumped, ran, lifted something heavy- thought I was going crazy. It broke down the integrity of my skin, I got sores and pain, eventually itching which all led to a diagnosis of LS- i do believe they are related. 
  • Posted

    I did suffer with this for a while . I now drink a lot of water to flush the bladder . First thing in the morning I drink a pint of warm water with half a large lemon freshly squeezed in it . Lemon turns to alkaline when in the body , so neutralises the acidity in the bladder .  I find this helps . It tastes nice as well and gives you vitamin C to keep away colds and flu as well . You won’t lose anything by trying . 😄

    • Posted

      That's exactly what I did Jacqueline, and it helped enormously. It also dilutes the urine and flushes out the bladder. In my case I found out its not LS at all. Just severe Vaginal Atrophy which unfortnately affects the urethra and you get a constant feeling of a UTI

    • Posted

      So glad you’ve not got LS . I’ve had biopsy so definitely have , and hate it . I do what the specialist tells me but sometimes it gets me down 😒

    • Posted

      linda, I started with AV. went for three years with no bothersome issues. Saw a gyn recently because of recurring internal itch. That's when she surprised me (to say the least) with LS diagnosis. My advice is to be sure to keep using the hormone cream. No sense adding another problem. Although not everyone with AV gets LS you don't want to chance it.

  • Posted

    I to have recently been diagnosed with LS and thought I had a outbreak turns out I have a raging UTI also along with outbreak both driving me mad 

    Any suggestions for the burning it’s getting me down the most 

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