Found out on Tuesday 14th May that I have T2 Bladder Cancer. Looks like its contained to the bladder muscle so having PET scan on Monday and start 3 rounds of Chemo on Tuesday.
Feeling calm now that I know what it is and where it is. The waiting for the 1st Cystoscopy was the worst.
I have to have bladder out and was hoping to chat with some 'Bag folks' and some 'Neobladder folks' to hear their experiences.
Just touching base and wondering how your PET scan went and how you're doing with the chemo?
Have you heard about our Cancer Connect program here at Cancer Council? It's a great little program where you can chat over the phone with trained volunteers who have had the same or similar cancer or treatment you are having. We have a number of volunteers who have had bladder cancer, even one with a neobladder, that might be great for you to have a chat to. If you'd be interested, send an email to firstname.lastname@example.org with your contact details and I'll have someone from the team contact you
Cancer Council Online Community Manager
PET scan was good as contained to bladder. Been lucky with nausea not getting to bad. Have to lose weight for opeation so that's not a problem at the moment. I'm a week into the second round of chemo and very cloudy in the head.
Was lucky to spend some time with and talk with some people who took me through the bag option. Plus found a great forum on FB - Neobladder Nexus. Got the monkey off my back by attempting a self catheterisation and the 'unease' disappeared so scheduled for a neobladder on 31st July.
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