CCR appointment (cancer care review)

So I had my CCR at my local doctors on Friday. 

With a guy called Craig, asking how I've been since being diagnosed etc, how I'm doing financially, how I'm doing mentally etc etc. 

Said fine on all counts really. Finances were not that much of an issue, as for the 6 weeks I got company sick pay and SSP so was only losing about 50 quid a week take home off my normal wages. I'm lucky in that I earn a decent wage being a lorry driver. 

I am probably around 1000 pounds less than I would have earnt all told with some loss of earnings and the first 3 days being on sick we don't get any pay for. But I've used up all bar 1 week of company sick pay this time alone. That resets in January unless I have to have time off and the company may decide to pay it for longer than the 7 weeks at their discretion.

Said he was happy with my take on things and my outlook with things, I'm lucky compared to a lot on here with just the one non invasive tumour and small and caught very early. Quick action by the doctors and hospital and all removed as I've posted about before. 

I can't do much about it other than try and be healthier and if it comes back or more come in different places then say lavvy, it's just a waiting game. Asked about any urinary issues or unusual issues etc. 

I'm back at work and just cracking on with life and see what happens in the long run. I did ask the consultant about chances of reocurrance and forget what he said percentage wise, but seemed to think my prognosis was reasonably good. But yet I'm going to be on surveillance for the rest of my life. 

Then Craig said after reading all my notes that the consultant and doctors had put, when I asked again that he seemed to think they seem to be expecting reoccurrence to be slim or whatever words he used. 

I know they can't give you any real useful info on how likely it is to come back, but that actually made me feel rather lucky to hear those words. But again I'm also not going to pin my hopes on it never coming back or even getting worse if it comes back. 

I have done a lot of research and looked into all eventualities and am as prepared as I can be for anything in the future. I just like to be as prepared as I can be. 

So all in all a good chat, I also suggested that I don't think that Linda the cancer champion should be ringing me every month for a follow up, there are people in much worse situations that could really do with the service more than me, so when she contacts me for the next one I'm going to suggest a less frequent follow up call in my case, I don't want to be taking up valuable time when at the moment I'm fine and nothing currently to worry about. 

I can't fault my team of doctors and surgeons and care guys and gals, they really have worked wonders with me, maybe I'm lucky in the area I live in but it's been mostly first class. 

I also know not everyone is that lucky and for those who are going through much worse I take my hat off to you all and hope for something much positivity for you all. 

So yeah just an update on how things were again after my op and stent problems etc. 

I feel back to my normal self now and just getting on with stuff as per normal bar the surveillance and cystoscopy's to come, the first one in 3 months post TURBT, so that will likely be in early Dec. 

I am also at risk of heriditary bowel cancer on my dads side, he died at 54 and one his brothers much much younger. It affects all the family on my dad's side sadly male and female, all we actually know is there is some genetic anonmoly in the bowel but that is as much as we know. 

So I also asked about how often I should be getting checked to that now I finally brought it up as before I just didn't want to know. He said do a fit test every 2 years and just keep an eye on any bowel habit changes.