Some of you may remember I came on here about a month ago getting cold feet about my planned brachytherapy .
I have just completed my 3 brachytherapy sessions and thought it might be useful to share my experience .
Session 1 lasted about 40 mins , internal examination and fitted for correct applicator size . It was quite uncomfortable where it presses on vaginal vault but doable for the 7 minutes of radiation . Afterwards it felt like I had had a smear test . In the week following had IBS like symptoms bloating, wind etc may or may not be related . Felt very tired but managed a fairly normal routine . Started to get quite sore and irritated vulval area .
Session 2 Felt quite rushed , different radiologist who didn’t hang about inserting the applicator . It was really quite painful , they checked that I was ok to continue which I did . Longest 7 minutes and glad when it was over . Afterwards bad cramping dull aching pains for about 48 hours for which I took paracetamol .
this time had a brown discharge for a couple of days . Still sore externally so used aqueous cream , told ok to use Canestan cream if itchy . Spoke to cancer nurse who asked radiotherapy to ring me but weekend and bank holiday so didn’t get a call back!!
Session 3 Very nervous at my last session today after last week , saw the senior radiologist who measured me in week one and we went through all the side effects I had been having . She was very gentle inserting the applicator and apart from slight discomfort from pressure at top of vagina it was a breeze this week . Got the delightful pink dilators and everything carefully explained
Follow up in 3 months
Managed lunch and a walk at a nearby NT property afterwards.
not too much pain now although they advised paracetamol every 4 hours for a couple of days . Bladder feels very irritated so drinking plenty and will keep an eye on that .
On reflection I’m glad I chose to have the brachytherapy despite the possible side effects as I want to give myself the best chance going forward .
I would like to thank others on the forum as it has been a lifeline over the past few months .
Now need to slowly and carefully get healthier and lose some of the weight I’ve gained after surgery and start to get some normality back in my life .
Oh and I won £200 on the premium bonds this morning so onwards and upwards .
Congrats on the win! A good omen? I have had painful bladder issues for years and I avoid cranberry juice as it only aggravates my condition. What I find helps is marshmallow. You can take in capsule form or teas and it builds-up the lining of your bladder. It may take a few weeks to work but helps bladder pain and irritability, alongside other standard treatments. Sounds like you're getting there - and good wishes for a full recovery.
Forgot to add that it's always a good idea to run it past your GP or pharmacist, in case there are any clashes with medication you might be taking.
There is also slippery elm and I also take antihistamines ( the latter recommended by my GP) as they reduce inflammation in the bladder, which will reduce pain too.
Good luck!
Hi Rethead
Sorry to hear that you had a few issues with the Brachytherapy well done on persevering, I was lucky I think with the team I had it was the same people and I was not rushed at all, I had no real issues during the treatment other than I had to make sure that when I ate after it then I couldn't venture far from the toilet , I am now 4 weeks post Brachytherapy and feel good other than I have since the end of the treatment developed a slight burning sensation internally and over the last 2 to 3 days started with an more intense burning sensation. I am hoping that this is the peek of the radiotherapy and it will calm down (fingers crossed) and if any ladies on here have had similar with the burning please feel free to shout , and I also started to have some days when I feel really tired, again the last few days seem worse .
Day 1 of the Dilators today, wasn't as bad as thought I told Alexa to play some relaxing music and set a 5 minute timer , only 156 weeks to go !! however I have noticed different hospitals give different advice mine said 3 time a week for 3 years , I have a friend who didn't use the dilators and she gave me a lecture on why I must use them so I will be trying my best to make sure I keep this up.
Good luck moving forward and enjoy the normality I am just starting to feel life is more normal. Oh and I also had a little win on the premium bonds, so yes onwards and upwards.
Linda
Hi there - thank you so much for posting as my three sessions are planned for August . Your session two sounds like a rushed smear test so you have my sympathy . I didn’t see your earlier post and will try and find it . I feel quite nervous about the whole thing .
Best wishes
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