
Bernie Foran (my oncologist) called me 10 minutes ago from Weston Park Hospital. My appointment for tomorrow had been put back 2 weeks, but I asked them to let me know my MRI scan results as soon as they have them.
They have them. They're fine. And that means - SO AM I !!
I'm told the term for this is complete remission (thanks to Hayley for that). I checked through my diary earlier today - and from my confirmation of diagnosis to today has been almost 9 months. Its been a hell of a journey, and obviously a journey that will continue until I'm back to normal (yes ok, Ive never been 'normal'
).
Of course I can never forget what the last 9 months have been about. I have lots of physical reminders, a chin like Buzz Lightyear at the moment with the lymphodoema and a huge scar from ear to chin. I've obviously lost a lot of weight, but feel and look stacks better for that. I lost a large nerve in my shoulder that means the kids now really enjoy tapping me on the shoulder and knowing I won't turn round (nice to be the source of entertainment eh!!)
I also have no feeling in the left side of my face. I can't lift my left arm over my head anymore - which means that Michael Phelps can rest easy knowing that I won't be challenging his Olympic record of 7 golds in the pool anytime soon. I also have a tiny scar in my stomach - a permanent reminder of the PEG feeding tube that kept me alive for 5 months. My mouth and throat are extremely dry these days as a result of losing a number of saliva glands which means that I no longer enjoy my food the way I used to - I have to wash pretty much everything down with a sip of water now. (Although I will give a mention here to Julie who promised me Beef Wellington right here on this blog and duly delivered on Saturday night with the best meal I've had since I started eating again - thanks Julie it was gorgeous)
On top of that there are the mental scars. I dream a lot about chemotherapy, and being told I have cancer, or its back. I get really upset when I see people going through what I've been through, and even more so when I realise just how lucky I've been. My good mate Dazzy G said to me on Saturday - 'How does it feel to have cheated death?' (He was slightly drunk at the time) It seemed a little premature to be asking, especially as I was still waiting for the MRI results so I didn't really give him much of an answer. And I still don't want to tempt fate by doing so.
I'm in remission - yes. I won't feel like I've cheated anything until I've been discharged in 4 years time - and even then I will always wonder. And nothing anybody can say to me will make that go away.
I will admit something on here now and its something I never told my Mum and Dad about for obvious reasons. When I was diagnosed by Mr Durham, the brilliant consultant who operated on my neck on Christmas Eve I asked him what would be my prognosis if I didn't have the surgery/treatment. He gave me 6 months 'maybe slightly more'. Which means that there would have been an excellent chance that I wouldn't be here right now.
I never once allowed myself to believe the treatment wouldn't be successful. I had brief fleeting moments when I considered writing letters for the kids 18th/21st birthdays, and Gina's wedding speech (should she get married one day). But I never did - because I thought that would be like giving in.
I've just read back what I've put so far - and I'm sorry if it seem's a little downbeat. Obviously I'm absolutely delighted with today's outcome. Now isn't a time to look back - it's time to look forward.
And I would encourage all of you to do the same - please humour me and stop what you are doing for the next 10 minutes. Then, consider how you would feel if you had been told there is a chance you might not be here in 6 months time. Would you do anything differently? If the answer is yes - then stop what you are doing, and do that different thing. (Cliche time) - this is not a dress rehearsal - its your life, you only get one (unless your a Hindu!). Don't put up with things that make you unhappy - change them. I mean it.
And then do me a favour - please. When you make those changes - tell me. I'm going to need something to keep my mind occupied now that I can stop worrying so much about this!! 
Thank you to everyone who has logged onto this blog. I have been absolutely staggered at the people who have kept in touch with my progress - I really can't believe there are so many people interested in what happens to me. In its busiest months over 2000 unique visitors read these pages - thats absolutely unbelieveable. Yesterday I spoke to a journalist who has discussed with me the possibility of getting these pages published. So, if you want to save yourself a bob or two - print it off now!!
All the very best to you all
Nigel xx

OK FAN BLOODY TASTIC!!!
Not good on the stop what your doing as im actually working for a change!! But i know what you mean i have had that in my head since you where first diagnosed and i changed things in my life for the better!
I no longer work 9-5 + additional required long hours for a company who dont give a damn! but work alongside a great partner (LOL ;-) ) in partnership working in something we both enjoy and work around family life!!! Yes we might not some months earn shed loads of cash but lifes good!!!
Really hoping the good news continues and you can get on with your life and work! ;-)
Kezza
x