I thought a quick update on this was in order. I think that peoples experiences can be useful when others have to go through the same thing. If this thread can help someone in the future then it has been worth writing. Well it is all good news so far and I have been given as close to "all clear" as I will have for a few years.
Just before Christmas I had my final MRI scan along with the usual blood tests and xrays (I was taking part in a trial of MRI scans instead of the usual CT scans). It was, as expected, clear. At the start of all this in October 2011 I had expected to be given the "all clear" after three years but I don't think it quite works like that. I was previously on a three monthly xray and blood test cycle with annual MRI's. But this has now been reduced to a six monthly xray and blood test, with no more MRI's. I think what happens now is that the test frequency gradually gets longer and longer over time. I'm actually glad I'm still being monitored because although I have absolute confidence that I am totally free of cancer now, I like the reassurance of being checked in case I have something else in the future. People sometimes ask me if I ever get worried and my reply is that I know I am (almost certainly) free of cancer but no-one else in the room knows whether they are.
I still haven't told my children what happened although I will tell them before my son reaches puberty (this is when he becomes statistically at a higher risk due to family history).
At all times I have tried to approach this with confidence and aside from the shock at the start I have seen no reason to worry about something I can't change. The only time I did get a little concerned was when I had a kidney stone last year. No stone was showing on the ultrasound and the hospital were overly interested in my testicular cancer history, treatment and when I was next being seen by my consultant. It was the only time I let the thought of it returning briefly enter my mind.
So this will probably be the last update to this little log of my treatment as I am now entering a "business as usual" period of testing. I am grateful to my family and friends for the support they have given me and eternally grateful to the doctors, nurses and consultants who have, at every step, treated me with the utmost compassion and care.
Perhaps the last gift that my father gave me, as I held his hand when he died from lung cancer in 2012, was the experience to take this disease seriously and insist on being seen by a doctor the same day I found a lump. People who have had a similar experience often say that it has changed them. I can't really say that but it has given me a different perspective on life and I find it very hard to get worried about little things anymore. However one of the side effects of low testosterone is exactly that so perhaps that is the reason rather than some grand change in perspective. I do miss getting genuinely excited about things, which I now find hard to do. But is that because of my testosterone, or is it simply me getting older and wiser? I don't know the answer to that. But I do feel different and I do miss having a genuine passion in things I do. But most people affected by this disease shouldn't worry too much about that becasue they are likely to be affected on one side only (I was affected on both, hence low testosterone).
Another side effect of low testosterone is putting on weight. That happened to me and I decided to get fit again in May last year. I'm now in as good a shape as I was when much younger and fit into trousers I never thought I would be able to again. But it does take hard work... again was that weight gain just due to age or the impact of low testeosterone? Probably a little of both.
So once again chaps... check yourself down there regularly and get seen by a doctor if you find a change. The same goes to you girls on the forum; check for lumps up there. And if you find something get seen immediately but be aware that it is indeed a disease that is treatable and very beatable. I was diagnosed with it at 43 years old. This is unusual and it is actually a young mans disease. So just because you are young don't put off checking; you need to check because you are young.
I wish you all the best...