New here but used to forums having been joint admin on a cricket forum for many years,
August 2020 and I saw blood, rang 111
April 2021 saw blood again - 11 again and was directed by doctor to go to urgent care unit, where I was given antibiotics.
May 2021 blood again, saw nurse and sample tests suggested infection so more antibiotics.
June and more blood. Requested to speak with my GP and she responded quickly and was seen at hospital two weeks later when I had a (Flex Cystoscopy) which went fine, I watched on screen and even saw my tumour. Dr said it looked new but, my symptoms started 10 months earlier...I was pleased because I thought slow growing.
Things then moves, telephone pre op and general pre op and in August 2021 I had a TURBT.
On the follow up I was told it was "aggressive" - I was surprised as I thought the time from first symptoms to diagnosis was quite a while.
On follow up Dr said aggressive but none muscle invasive. Meant more TURBT's but was treatable.
I had other experiences which I will share when I find my way about, Thank's to the people who answered my original post.....
Hi ern007, you might be interested in the first part of my husband's saga. Quite a number of years ago we don't even remember when and have never tried to check, he was troubled with frequent peeing. GP sent him to local hosp where urologist booked him in for an overnight stay 'so they could have a look to see what's going on under GA'. He was really rough afterwards and had a catheter in, which I don't recall any warning about. The surgeon said ' oh there were a lot of growths just like seaweed but there were more than we thought there would be'. No-one EVER said cancer and the only follow up was a flow clinic nurse six monthly; after he forgot to go one time being still at work that was it, nothing more. Meantime years pass, married daughter up north announces we are to be grandparents and as I'm under notice of redundancy we decide to retire north to be near [at 72 he' was happy to pack up his retirement job]. Up-at-night gets too annoying so off to new GP. After some delays a flexi shows entire bladder in his own words having seen while I sat outside " looked like inside-out cauliflower" with papillary tumours. But take heart that was 4 years ago and whilst graded high risk of recurrence G3 it was still only pTa non invasive and after treatment it's just regular check-ups.
So I believe he had had cancer for years and years without it invading the muscle which could prove this is possible, although others are less fortunate, and I personally think you were right about yours..
best wishes,
Denby
Hi Denby
As far as I know, I just had the one tumour, as far as I know. I say that because at times everything is not clear..
Nice to hear your husbands tumours are "none muscle invasive" - and have not spread. It must have been a relief to hear, considering what they found,
I still get the frequent trips to the loo, if anything more so.
I have another cancer it seems in my toe of all places, I should have gone to Blackpool yesterday but told them to get there by 8 am was not possible from where I live. Poor sleepers and night time trips to loo means I never venture to drive until my tiredness has worn off. So they managed to get me in at my local hospital on New Years Eave,
Back to TURBT I had spasm where I was desperate to urinate despite catheter, I was told to just RELAX really was a nightmare, The morning after the op I hade Chemo direct into bladder via catheter, So far so good.
Later after the catheter removed i was told pass 100ml of urine then I could co home. Sounds easy..
Noooo - After two hours I was not there or after three - I drank and drank and drank - Yes!! I was there, going home after bladder scan. This is not the end of the saga I did get home but, I may find I can finish this episode, if so I will..
Good Luck, best wishes...Ernest
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