Urinary issues after brachytherapy

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I had PDR brachytherapy in late December 2022 after my hysterectomy in early October. The first few months after the treatment I felt a little tired and slightly sore but otherwise not too bad. In April I started having a burning sensation when I passed urine, a constant feeling that I needed to do so and a burning sensation just above the pubic bone area. I went to my GP's and the ANP gave me antibiotics as there was an infection in my urine sample. I felt much better for a couple of weeks but then the symptoms returned albeit not quite as severe as the earlier episode. The ANP tested my urine, and sent it off to Pathology but there was no infection. I know brachytherapy can cause bladder/ urinary issues but thought these would have happened early on rather than 3 months after the treatment. I've e mailed my CNS for advice as I still feel uncomfortable but wondered if anyone had experienced similar issues. 

  • Hi SH53

    I am sorry to see that you are having some urinary symptoms that are concerning you. You have absolutely done the right thing by contacting your doctor and being checked/treated for a potential urinary infection. I am sure that your CNS will be back in touch soon with advice. 

    I did not have brachytherapy but I did have external beam radiotherapy for my womb cancer. I was told that my bladder may be irritated by it and that this may not happen straight away. She said sometimes after radiotherapy things take a while to settle. During radiotherapy I mainly had bowel effects however after it had finished I did have some bladder irritation. For me it was slight stinging, feeling a bit uncomfortable, going a bit more often and sometimes a little urgency. Staying really hydrated helped and it did resolve a few weeks later. Occasionally I still get a bit of a sensitive bladder- a bit like when you feel that you may be coming down with a UTI but it doesn't actually happen- if that makes sense.

    I hope this helps a bit

    Jane

           

    Macmillan Support Line - 0808 808 00 00, 7 days a week between 8am-8pm

  • Hi Jane, thanks for your reply and support. Yes it all makes sense!  I think it could be irritation to my bladder as I sometimes get a slight twinge in that area when I start to pee. I thought any side effects would start immediately but I've since read, on a reliable website, that they can crop up some time later. 

  • The way it was explained to me was that the radiotherapy goes on working for sometime after it is given. Things peak around a couple of weeks after then should start to feel a bit better because you are not having the treatment. The cells take a while to recover and to have the new healthy ones grow. It is then that sometimes effects can pop up until everything settles. 

           

    Macmillan Support Line - 0808 808 00 00, 7 days a week between 8am-8pm

  • Hi SH53

    I just wanted to share that I've had similar problems. I had a hysterectomy after being diagnosed with womb cancer followed by chemotherapy....once a month for 6 months. Unfortunately 7 months later, I was told it had spread to my peritoneum.  This was followed by 4 more monthly cycles of carboplatin then 18 weekly cycles of paclitaxel.  

    Over the last few months, I too have had cramps, lower abdominal pains and an urgent need to go to the loo, and was treated for a UTI. Testing later showed there was no infection although the antibiotics did help. I've also had problems with my bowels and obviously I worried it was something more serious. I was told it is probably the after affects of the treatment. 

    Hopefully you will soon feel better but maybe not worry too much. Of course if you feel worse, then contact one of your health care team.

    All the best 

    Helen x

    Helen 
  • Thanks Helen. Sorry to hear you've had some unpleasant side effects after your treatment. I live on my own so can overthink things sometimes! Thank goodness for this forum where we can open up about our concerns and share advice. 

  • Hi SH53

    I'm pleased if my similar experience has helped to reassure you. 

    Take care 

    Helen xx

    Helen 
  • Hello SH53 

    I have read that Brachytherapy can make you feel like you need to wee more often or urgently. You may also have a stinging or burning pain when you wee. This is because the applicators and radiation can cause bruising and damage where you had the treatment.This can happen after treatment or few months later. My own experience was good at first, then couple of months later I started to feel irritation and sore in the genital area which I was treating as thrush with over the counter meds. It seemed to get better and returned so sought help from doctors who prescribed tablets pessaries and creams, again it returned so next appointment doctor did a swab and it came back negative for thrush, so she prescribed a topical cream which has much improved my symptoms. At it's worst, it burned when I passed urine.

    I can admit that my internal area is definitely changed since my brachy in August 2022 and feels more delicate, I sometimes use the dilators but as I much prefer the natural way we have to be more careful if you know what I mean.

    Hope this helps in some way x

    Madesp 
  • Thanks for the helpful information. I was reasonably OK - apart from some soreness - for the first few months so thought I managed to dodge any side effects. However, it does seem that they can crop up when you least expect them. At 70 I'm well passed the menopause, never had children and been single for 15 years so, sadly, having to rely on the dilators. It's been challenging, to say the least! On my post op letter even the surgeon commented that I had 'a narrow vagina'! Wasn't really shocked or offended as she was simply stating a physiological fact. The joys of gynaecology! 

  • Hi SH53
    I'm really sorry to hear about the pain and discomfort you are experiencing after your brachytherapy. I had brachytherapy March 22 after womb cancer (1a grade 3) I had a radical hysterectomy and chemotherapy for 6 months. I experienced some soreness at the time and that seemed to pass after a few months, although I did delay using the dilator. I wasn't ready psychologically and I had to wait a number of months until I was ready mentally) I have experienced some urine incontinence and needing to go to the toilet felt a lot more urgent and more frequently, especially at night, much more in the first 6 months.
    I usually wear an incontinence pad and I did not experience any soreness after a couple of months but I made some changes. I limit my caffeine to a minimum of 2 drinks before 12.pm -1.pm and I drink predominantly decaf coffee now and Yorkshire tea (up until 1.pm), then after 1.pm I drink decaffeinated green tea (yes, I know it's a diuretic, oh the irony!) I very rarely drink alcohol (only on special occasions) as it makes me want to pee a lot more especially through the night. This was already happening 4-6 times a night, so my sleep was and is still quite broken. And I'm trying to do my pelvic floor exercises on a more regular basis with some days being more successful than others. 
    However, I have recently had some soreness that has increased and I think it's because the pads I was using which, were not my usual non perfumed kind, had a layer of aloe vera as they were for periods. I don't use perfumed products as a rule because of my skin being much more sensitive in my vagina, since the brachytherapy and my age as a postmenopausal woman of 57 years old, but I had to buy these out of desperation. I have since been able to buy some non perfumed pads and the soreness has abated again. So, if any ladies use a panty liner or a pad, it might be worth checking to see that they are not perfumed. I hope you symptoms improve over time and I think it's great your keeping your cns nurse updated with your concerns. 
    best wishes to SH53 and all the ladies on the forum
    Bridgpond89
  • Thanks for the reply. Sorry to hear of your ongoing problems, you've had a difficult time. The post op treatment can be very tough on our bodies - and souls - and, on reflection, I probably underestimated  the side effects I might have. Cranberry juice has been recommended so I'm going to try that plus I'm going to switch to decaf coffee. I've lived on my own for 30 years and was always quite happy with my situation but it can be more challenging when you've had health issues. I've joined a local Yoga group which has been very beneficial both physically and emotionally plus I've met some lovely ladies. I always wear a pad for the class just in case of any little accident! 

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