On last scan about 4th I think I am down to have another Tula and it was discussed thst I should have 6 week course of Mytomycin?.
Can anyone who has had this give an idea how long after the tula the chemo commenced?.Great difficulty in getting in touch with the urology dept. Feel a bit of a twit and thinking ahead as I consider myself very fortunate that the cancer is non muscle invasive and stage 1 but I like to know whats ahead to organise myself.I must of heard wrong when told at the scan that lazer treatment followed by chemo in the ouypatients. But appt letter doesnt mention chemo.
Many thanks and wishes to you all
Hi Sunshine forever . Not had Tula myself, but we know from being on here that they have to leave it for a few weeks for the bladder to completely heal before starting bladder chemo. I am sure someone with experience will be along to help. Best wishes.
Again not TULA but TURBT 24, couple of small recurrences this year during rigid cystocopies. At my last one in Jun several small and one large recurrence, at my next follow up for results which was early aug i think, was put straight on to mitomycin plan as soon as possible. Started early to mid sept. So 1 monty tops from the day I was told I'd be having it.
It doesn't necessarily mean much. It really depends on the doctors that are treating you think you will benefit from certain types of treatment.
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My name is Simon.
Much love and hope to everyone past future and present.
I also hate autocorrect and hope people can make sense out of my posts when it changes half the words I type.
Don't want to rain on your parade, but my fist tumour was 1cm grade 2 low pTA, aka no muscle invasive and low grade.
Surgeon said little change of it coming back caught early etc.
Went nearly 6 months with nothing coming back then 2 recurrences mostly small tiny ones it seems, but enough for then to go let's try and nip this in the bud somewhat.
It's the calls they make based on heat they find, experience etc.
But I've just been through the wringer for it as had a another check up and had biopsies taken.
So no one size fits all generally they will have certain plans and go certain ways as oar for course.
I'm like you I tried to be aw prepared as you can be for all eventualities.
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My name is Simon.
Much love and hope to everyone past future and present.
I also hate autocorrect and hope people can make sense out of my posts when it changes half the words I type.
Thank you so much for info urology team are great but sadly nigh impossible to get them respond on the telephone!
Thank you Simon for info guntimes ahead for me! Keep wellx
Wow meant funtimes ! Not qjite ready to be put down yet
Hi Sunshine forever,Have you tried emailing urology ? I never got anywhere phoning but an email gets a response.Love Jane x
Thank you Jane the old brain not working too well hadnot given that a thought! Will dox
I even got a phone call from my cardiologist after I emailed so it’s worth a go.x
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