Sunday, August 16, 2009

*** Scar Wars VII - Bladdered & Bruised ***

Scar Wars VII
In a Galaxy far, far away
Our hero Dave-Sky-Nando* has to endure another trial by cystoscope.
Darth Urologist and her team have a plan to flypast the potential moon (don’t drop those pants Dave) to the planet Bl’dar and entering via a narrow well guarded pipe gain access to the inner lining and there search for mutant and militant cells of insurgents of the Atypia, Precancer and Cancerous tribes.
Any cells of mass destruction were to be treated to shock and awe tactics of the allied NHS forces.
The only way to mount this attack and fly the cystoscope through the narrow and tortuous passage is during sleep induced by her evil henchman Darth Anaesthetist. Our hero, overcome by mind bending drugs and sleep inducing chemicals is overpowered once more and the Empire does its worst.....

Dave-Sky-Nando, Jedi Master, Cancer Survivor and all around good guy, entered the concrete and glass citadel and the ward that is the pre-theatre preparation centre. He was pleased to observe that at last, the old surgical operating gowns “for Hospital use only” which – let’s face it are not a fashion statement, aren’t big or clever and didn’t exactly fasten properly leaving the patient to “moon” those within eye shot of the wearer had finally been consigned to the incinerator. The new, rather tasteful gowns are two tone blue, that tie up properly and overlap sufficiently so as not to leave the rear exposed unless you want to wear them that way.

I must be getting used to it as blood pressure and heart rate were high but not out of bounds like normal. An MP3 player with classical and easy listening music assisted the 3 hours between admission and being wheeled to theatre to go reasonably quickly.

The ritual of going through your details many times to ensure they have the right person and the other various checks are undertaken at this time:

  • False Legs or limbs?
  • Metal work in body?
  • Jewellery?
  • Loose teeth, crowns, caps?
  • Mobile phone, hidden camera?
  • Picture of the Queen, comic or other publication?
  • Sharp wit?
  • Uncut toenails?
  • Aircraft carrier, space station?
  • Criminal record (Mcfly, Robbie Williams etc)?
  • Machine gun, IED, tank?
  • Any drugs, cigarettes or alcohol?
  • Any scissors, water, lipstick, packed lunch or other dangerous stuff you can’t take onto aircraft?

Once you have convinced them that there is just you under the operating gown they finally leave you alone after you have signed your consent form.

This time and probably for the first time, I let things just happen as it is going to happen at their speed and not mine, I can’t influence anything including their schedule and the way they do things at the Hospital. I see my consultant who has a quick look at the notes and assures me as the anaesthetist checks me over that it is the usual inspection and do I have any questions. I don’t except that when I finally find out that the Registrar did me last time and I look into the eyes of the butcher who gave me such a rough set of biopsies then. I don’t know at that time, but I soon find out that he did me again this time. His trademark being that you end up with a catheter for his cystoscopies. A lesson from some of my Jedi friends might be in order....

Wheeled to theatre the procedure is run through again, checking who you are, if you have any contraband secreted about your person. I’m Ronnie and I’ll be preparing you. He did well and the cannula went in easy enough and the check list was mechanically run through whilst we waited for the theatre to become empty and for the anaesthetist to come in and deal with.

RU1?

RU12?

IM1 n U?

IM12,

U2?

Stupid Droids :-)

A guy who looked like Yoda tipped up and he was the head anaesthetist – I had met the junior who was also there. “”Sleep dreams sweet put you this will” said one, the other added “holidays nice you think now of”. “Ouch” I said as he started doing something nasty with the back of my hand where the cannula was and I could feel quite sharp pains in the vein there. They then stuck a mask on which was a first and so a combination of things eventually saw me off to sleep.

The next thing I remember was waking up, oxygen mask on and being really pissed off that there was a catheter in me again. It makes you feel as if you want to urinate all the time but can’t. It is annoying when before you haven’t had one and then you wake up and find that they’ve pulled you around enough for a second time to do it again when before it hadn’t happened. You also know that you aren’t going home that night like they told you – many times before - that you would. I was already pretty much sure that I’d be in overnight as it was an afternoon slot.

Two hours after going down to theatre, I was in a ward, without my belongings which were somewhere else as I wasn’t in urology where I should have been but another surgical ward. At least it wasn’t the one I was in last December which really was the ward from hell. Here the nurses all seemed very nice and after the two others patients I had shared the pre theatre ward appeared, our belongings turned up. Mind you, as I was all bagged up I could hardly move, another reason I hate catheter is that you are really limited in your movements. I had to wait until Mrs. F. turned up to get my stuff out of my bag especially my MP3 player.

The automatic bed was working well but again I had real difficulty trying to adjust my posture as I had this bloody tube hanging out of me.

It was on return to the ward that the full horror of the next 15 hours or so became blindingly apparent to me. The chap next door to me was obviously struggling. He wasn’t a urology patient but had just had a violent reaction to morphine and wasn’t allowed to eat or drink. However, he had what I can only describe as tourette’s syndrome. Up to 4 or 5 times a minute for all his waking hours he would be moaning, groaning, sighing, ooowwing, arrring, coughing, spluttering and so on. Now the nurses realised and tried their hardest to sort it out and tried medication etc. However, on and on it went. I used my MP3 player to best effect that I could without making a nuisance of myself and finally at 2 am he finally fell silent. I managed to lie on my side, deaf ear up, and get a few hours sleep. At least at about 4:30 when he started again I was sufficiently with it to turn on my MP3 player and try listening to that. I must note that my MP3 player gave up the ghost at about 9am and so if there is a next time I ought to take both players as this one needs a USB port to recharge it.

At 5:30 I had my vital signs done and good grief, 139 over 89 and 86 heart rate – amazing almost normal for me when at home where I try and keep 130 over 90 as a maximum. They then took out the Catheter which was a relief but it was a large catheter not the small one I had last time so I felt quite sore. I had been bashing the water back since 4:30 and so was ready to start to show them 3 clear urinations for which they leave a bottle. I was able to do two before breakfast and one afterwards. However it took over 1 ½ hours between sorting that out and actually getting discharged from the Hospital. I had to slightly force the issue but I was pleased to get out and get home.

The best news of all really is that it all looks clear, no red patches or anything else unusual they still took a full range of biopsies though. The lab reports I hope fully support that and even more than that I hope that this really is the last time I have to go through these full biopsies and cystoscopy again. Mind you, I thought that the last time until I saw my consultant. They also said they wanted me to do more BCG but then changed their minds. I’ll find out in a few weeks when I see my consultant.

There’s a bit of a mess where the cannula went this time and I am a bit tender today – I guess they smack you full of pain killers and today is the first day that bruises are coming out and that I am actually feeling sore in all the places you really don’t enjoy being sore in.

This time I knew the drill and what was expected of me and in both pre-assessment and the main operation itself, I expected things to go at their pace and not how I wanted them to, I drank plenty of water before arriving at the Hospital and all the time (when I was allowed to) which meant passing the tests and irrigating the bladder was assured. I was still slightly put out that they managed to end up sticking a catheter in and one of the big ones too. If I never have another one it would be too soon.

In terms of how do I feel about it now – well – I am still taking in the fact that it is clear and I am not absolutely certain what that means. I mean it looked clear last time but they found atypia. But if it is clear then I think that I go onto a maintenance holding pattern. I am hoping that this is flexible cystoscopies but there is a nagging doubt in the back of my mind that thinks it may mean I have to continue to have these full versions for many years but with greater periods between each one.

My continued thanks to my family and friends both online and offline who continue to look out for me and send me best wishes and prayers.
I hope that there won’t be a Scar Wars VIII.

*A creation of Steve Kelley Inc. :-)

Saturday, August 15, 2009

Bath and Bed

See if I can soothe away these aches and pains where they throw you around in the operating theatre.

All good fun but my back and groin area hurt as do my arms which they no doubt shoved somewhere. Where the cannula has come out looks a right mess too. Mind you, not as bad as the last time - at least the staff knew what they were doing and were pleasant and civil.

A good night's rest without the tourettes wittering of the guy in the bed adjacent to me tonight thank goodness.

Home

Tired, slightly sore, did I say tired :-)

However, after all of that, little sleep, catheterised (again) and delays getting home the upshot is that things look good inside Mr. Bladder and they still took biopsies and still pulled me around a lot. However, I am comforted by "We don't want to second guess the lab results but it looked clear" will certainly be something to hold onto until the out patients appointment in 2 or 3 weeks time.

Oh yes - and I'm tired - Scar Wars VII will explain all :-)

Friday, August 14, 2009

Another hot one

Another day likely to reach 27 C and the hospital will be like an oven. Hopefully they will have some fans around this time. It is at least air conditioned in the theatre and corridors.

Just got the MP3 player all loaded and I am now plugged into some music which is nice as that relaxes me.

Still not too bad although my blood pressure readings and heart rate are all up - what a surprise :-)!!!

I'd better go and do my packing and pretend that I want to go and get this done. At least the music is sorted out. I have a book that I can actually read without hurting my head and I just hope that I don't have to hang around there too long today / tomorrow.

Another Judgement Day

Arrives and I have got up early, had a shower, had my light breakfast and I am now on water up until 11 when I will head off for the Hospital for my 11:30 appointment.

A little churning in my stomach, a few nerves of course but not bad. This time tomorrow it will all be over and I then have to wait for the outcome. I might get a progress report based on the visual. I want to hear that everything looks alright of course. I'm not sure how I would feel if it were a recurrence, I'd have to take that and think about it.

I'm loading music to my MP3 and I have decided not to have any of the stuff I had when I went in the first and second times as when that happened I had cancer and of course I don't now. There are a series of songs that I associate with that time and whilst I like those songs they do make me feel quite strange these days. So searching for other sounds to listen to. Plenty of classical and less rock and roll.

It is just 3 hours away until I go in and I haven't packed my bag and I'm going to leave it so I have things to do in the next few hours. I'm going into my quiet, lock me away, don't talk to me mode right now and I lock myself down into myself and become quite monosyllabic in responses as I'm just not feeling like entering into a conversation. I'm sure that outwardly I will be pleasant enough but in reality I am just shutting myself down and keeping within myself.

Weighing in with the NHS debate

Interesting the debate over our NHS in the USA. It appears that, as in every argument, the lobbyists have been hard at work and fact and fiction abound. The report I just saw was meant to be representative and yet it portrayed those interviewed as just plain bonkers. I'm sure the editor felt that it was in our interests to see these poor confused Americans who had no real idea of what our system was really like and quoting spurious figures as facts about death rates. If they were true none of us would be left on our little island.

Sure the NHS has problems but no one needs to fund insurance and everyone can have treatment. There may be some issues with how it has evolved and inefficiencies and costs and budgets are all over the place, it doesn't mean that people die or that it is somehow third rate. What I'd suggest everyone does is look at the UK and other European systems and see how they work. Some of the French Hospitals are fantastic. The Scandinavian countries also have an incredible record in this area.

The argument shouldn't be about whether you want an NHS in the US it should be whether the way it provides equality for all can be used as a model. If you have ever read Steve Kelley's blog you will see that there are fundamental differences in the way healthcare is delivered and in the US there is more choice and things are just massively different. However, we both survived and we are both on different ways of being treated. None of us is saying which treatment is the best as the results are the same and despite my pointing out the issues that I have with the system, it doesn't mean, as some were stating on the TV that there are massive problems at a grass roots level.

Anyway, as I'm about to go into hospital today it was perhaps going to be on my mind. I'd just wish someone would deploy some facts to the US citizens so they had accurate information to base their decisions on. It appears that those who have most to lose are providing only one type of bullet and the opportunity to have a balanced argument cannot happen with only part of the story provided for the debate.

I suppose I ought to get to bed

It is after all 30 minutes past midnight. I just feel asleep downstairs and came up here after a nice meal out and a few (not many) drinks. Just about to turn in and I must be up early to have something to eat before 7:30 I can then get myself ready for my 11:30 appointment.

Feeling OK, quite mellow about things really. I'm quite impressed that I am quite so chilled about it this time. I just hope that it lasts and I look forward to getting this out of the way as soon as possible.

Good night.

Thursday, August 13, 2009

An evening out to distract me

Just what I need a good evening out with the family and celebrating Ls 16th birthday. I will eat well, have a few drinks, sleep well and be ready for tomorrow. I am also distracting myself loading up my MP3 player and pottering around getting ready tomorrow.

Not too worried about it really this time. I know the score, I've done it before. Worrying isn't going to help me and I'm back into the right frame of mind.

It looks like all of the BC warriors are going to find out their fate in the next few weeks. HK is clear - brilliant news and has three low dose BCGs to contend with. Steve is due up for his scope poke and peek in about 3 weeks time.

Anyway, it looks as if we will be out of here in 20 minutes or so and I had better go and get ready - or as ready as I will ever be. The Bank of Dad and my credit cards are all I need :-)

Last hours at work

Are dragging by. I've a few things left to do and I am reliant on others to do their bit to release mine. So struggling along with 5 minutes works to do in the next hour and a bit!

I'm still reasonably positive about tomorrow. I know it isn't going to be great but at least I know what is coming and at least in a few weeks I'll know if everything has been successful. I was amazed to hear that a friend of mine is still having the occasional full set of biopsies. He has been receiving treatment for 10 or more years and is on the "old" regime.

Here's hoping that things get moving in the next few minutes or else I will be bored stupid. I also want to get packed up here so I can get home and take L and the family out for a meal tonight. That will take my mind off of tomorrow.

Wednesday, August 12, 2009

Attitude

My attitude has definitely changed about this particular operation. It IS different to the last one. The last one was to make sure that the maintenance had done its thing and that there was no recurrence. That was 8 months ago and now this one is to make sure that there is no recurrence as I haven't had any treatments since September of last year (or thereabouts), almost a year without the BCGs.

So my expectations are much different to the previous which looked at how treatment had gone. This looks at how not treating me has gone. We now see if leaving things to their own devices has actually left my bladder - clear or not? If this is clear then we cross another bridge, change our roller coaster ride and move to a different level once again.

The whole feeling is different because I haven't just had treatment and need to see what has happened. It makes for a different approach to what you are having done and why you are having it done.

I'm hoping but not banking on this being the last one of these full operations but I do also have to realise that I did have an aggressive form and so I might have to come back for more of these operations in the future if my team and my consultant deem that necessary.

At least I am not as uptight about it as I have been - unless - of course - they turn me away - they didn't think that was likely this time as it is a quieter period.

Perhaps it is just something you come to accept after a while, it is now routine and may be for the rest of my life. You just have to get on with it and accept it. I like the fact that lots of people think I am being quite good about it all and keeping my sense of humour. The answer must always be with cancer, you have to rule it and not let it rule you.

Tomorrow is a good distraction

It is Ls 16th birthday which is very special and a milestone for her. She can now have her ears pierced with our blessing and that is lined up and I am taking the family out for a meal tomorrow night. It WILL NOT be entitled the last supper either.

I am most impressed with her finances in that she saved well over £4,500 to go on her trip to Argentina and almost all of that is money from work, paper rounds, bag packing, boot fairs and sponsored events as well as birthday and Christmas money etc.

I'm feeling quite laid back about Friday, noticeably so this time and I can't imagine why that would be. Even on Monday my blood pressure was reasonable (considering) and I wasn't quite as bad as I normally am. I'd hate to say that I am getting used to it, although I do know the ropes and I am an old hand knowing most of the Urology nurses by their first names as well as Audrey who is the pre-assessment nurse. All of them are just great.

I surprise myself with how relatively calm I am writing this and I hope that I will continue to be able to keep this level of calmness for the next few days. I doubt that I will come home on Friday but if I do I have assurances that the party will be dispersed early. I'd actually, on this occasion rather not be a party poop-er.

Mrs. F. told me that my next door neighbour isn't well again. He had a lung removed with Lung Cancer and looks as if he may have some sort of infection but he is going in for X-Rays. Fingers crossed for him.

My Open University colleagues dropped me a line - it seems many of them passed and they are arranging for a meet and a drink which I do hope I can make as I was disappointed not to complete the course. It would be nice if the Hospital actually don't beat me up and I can make it. They all sound very proud and excited about it - which they should be it was a great looking course and I just wished it could have turned out different.

Tuesday, August 11, 2009

Getting Ready for the Operation

I must remember to sort out my MP3 player and get myself set up with a book. Last time I wasn't expecting to be in overnight and I ended up with a catheter and an overnight stay. Depending on who performs this one and what they find when they peek inside will determine how long I am in for. I really don't want to be waking up to see myself all plumbed in to a load of bags as that will mean either they've puncture my bladder or they found tumours and cut them out.

I remain quite positive about this still. I like it that most people think that I am being very brave and good humoured about it all. I suppose I am - and I have to, there isn't really any other way of looking at it is there? You have to take it as it happens and I can't do anything about what they find inside.

I see that HK in Toronto had his Cystoscopy today so good luck to HK for a good result. It is nerve wracking and a bit like waiting to see if your lottery ticket has come up except that in this case you desperately hope it doesn't come up :-)

Liked the last one of the Gold Room? How about a Golden Roof


Click on images to make them larger:


This is the entrance to the Peterhof Palace some 40 minutes drive out of St. Petersburg on the Gulf of Finland. If you think this is amazing, wait until you see the fountains. I think I can see after just a few palaces like these why the had a bit of a revolution! Just amazing and these aren't all the fountains either, there is a whole park full of them.









Another Photo - The Gold Room in Stockholm City Hall


Adjacent to the Hall where they hold the Nobel Dinner is this wonderful room. It is made up of 19,000,000 individual mosaic tiles. The picture just cannot do it justice another place that was close to awesome. Consider how long it would take you and a team to assemble and set 19,000,000 mosaics. I have enough trouble with a 5,000 piece jigsaw :-)

Did I mention that the dreams were back?

It seems to be that the brain goes into overdrive just before an operation. I had a dreadful night's sleep last night and loads of strange dreams. None stick in my mind apart from the hanging in the woods the other day but these were just unreal things going on.

At work at the moment, just waiting to go out for a drink with friend and catch up on his news.

Monday, August 10, 2009

Contact from our on board party

It was nice that we had a nice bunch of people at our table on the cruise and one of them sent through some photos this evening so I have printed those off. Finally I get a photo of myself on holiday. The on board photographer took a few but they were pretty contrived things and not at all what I'd have liked and Mrs. F. no longer takes photos!!!

So a few of us on at our dining table and up in the night club. That's nice as at least I may have a few photos for my mother who likes that kind of thing.

It is a strange thing but I have almost completely turned myself off sentimentality now. It is most bizarre but it isn't important anymore to have photos of when I was younger or any of the history stuff that I treasured before BC. I watched a few old videos of the girls the other day and it did nothing other than upset me and whilst it was nice to see and remember those times it all seems like another world to me now. Some huge lump of my life got ripped out and thrown away when I got cancer. I hope that it is transitory and that all these things I have cluttering up the house and gathering dust - for that is what they actually do - make come back to mean something to me later on. Nostalgia not being what it used to be perhaps? :-)

When I say upset me - it actually means that I beat myself up about almost anything that I see. I wasn't a good father; I didn't spend enough time with my kids; dah de dah de dah.... You know anything to beat myself up and that, at the moment, is the way it is. If I do look back I find myself giving myself a hard time for drinking, smoking and all the other excesses of my youth and some of my adult life too. I argue with myself that this is what you do and that everyone smoked and all of this sort of thing and I blame myself for my situation and for not having achieved some sort of imaginary high ground that my mind tells me I should have done. It is a strange thing n'est pas that your brain which belongs to you actually comes out against you and beats you up with such painful thoughts and vicious accusations. My brain is far worse than any bully or masochist :-)

I'm not sure why any of this should be, it just struck me that the photos I have don't do anything for me like they used to. Almost as if the past is the past. Perhaps things have changed so much that what they old things represent isn't important anymore. If these things aren't important anymore, I still have to find what is important of course. That perhaps is the next part of the journey and one that will be made easier if the results are good after Friday's operation.

The answer I think is that I am important but I can't easily live with that. I can't easily accept that I am the centre of my own universe. My family and children are important - but they have all just proved they can go off on their own and even at a young age have planned, worked for and undertaken journeys and adventures of their own.

It goes back to the recent dreams (they have returned pre-operation - including the nasty ones) and my own review of what "value" I am now to my family unit? It is a wrestle with my own self belief and self confidence and it relates to where I am in terms of living, treatment and what has happened to me in just three years. I'm in no doubt that this is just another phase you go through when you survive BC. The old survivor syndrome and why did you spare me question?

A few days at work and then Friday beckons - I hope that my surgeon will once again be able to tell me that things look clear and that we can plan the next steps in my journey. That being the case I hope to drown my brain with beer (Thanks Homer) and start to sort my life out - it really can't be that complicated :-)

Well that was OK

I walked up and got seen as I walked in which was good. A quick new set of swabs, urine sample and it was on to having a laugh about my blood pressure which was good as I had measured before going at 131 over 85 with a heart rate of 82. They got me at 150 over 95 with heart rate of 108. But Audrey knows me and that's OK.


Doctor was great and all tests etc were OK so I go in on Friday. I was finished in less than 30 minutes. I think I ought to just get dropped off next time (if there is a next time) so that I am not quite so hot. It is a 20 minute walk at my normal speed but I did it slightly slower at 25 minutes. Even so, I was a little sweaty when I arrived.

It was a completely routine thing today. I knew exactly what to do and when to do it, the ECG machine behaved itself and I managed a couple of pints at the pub on the way home as a reward for having my blood test which, as regular readers may know, is not my favourite thing on the planet.

So all is now set for Friday. the Doctor said that I might go home straight afterwards. I said that if they managed that it would only be the second time and that the butcher who did me before meant I was catheterised overnight which had been a first. Hopefully he took note of my comments. I bet that they will let me go as it is Friday and it is about the only time with L's party that it would have been good for me to be in overnight :-)

Not long now

Do I walk up there or get a lift this time? Not sure but a slow walk may be useful. As long as I don't sprint up there and get all out of breath again! I can always walk back via the pub :-)

I just went to do the MRSA swab tests and the liquid that they suspended in has hardened so I cant get the swab into the tube!! So much for making things easier.... Doh!

Now I'm feeling a little bit deep breathy - exhaling long and hard. I don't suppose I'll ever get used to it, its just the way I am.

Further Images


This is St. Petersburg and the Church of the Spilled Blood built over the spot where Tsar Alexander was blown up by a terrorist. It is a truly remarkable place. The Photos just don't do the place justice - for some of the places the word awesome can be applied and almost made to work.... The Mosaic work inside and the stone marquetry are unbelievable.

The Countdown Begins

Not the Final Countdown I hope :-)

In a little over 4 hours I have to have my pre-assessment and Friday I have to go in late so that means an afternoon operation. Not sure a Friday is a great day to do it. One minor blessing is that L has her 16th Birthday party that day in the garden here and so at least I don't have to be around for that. Last year it was a nightmare to sort them out and get them out of the house/garden. Apparently she was none to pleased about the way I spoke to and ordered people out but then - it's my house and I don't take kindly to having to tell anyone more than three times what I expect them to do.

I'm reasonably calm at the moment however and I feel OK. Whilst I may not be looking forward to going in, I've managed to rationalise it in my mind and I suppose that I just have to accept that this has to be done to be absolutely certain that things are progressing well.

I remember being quite put out that it wasn't last time I had it done as I was certain that it was going to be the last operation and that I'd be having the flexible cystoscopy done. As it is I am having the rigid cystoscopy and so they have to knock you out for it.

I am hoping that if this is clear, the next steps will be to move onto that observation stage. At the moment they are checking because of the Atypia found last time. Better safe than sorry.

I also wonder if, because of my age, they are making sure that things are OK and also that I can probably handle yet another operation. I still can't remember how many this is - so perhaps I ought to tot them all up and stick them in some sort of league table so I can remember. Maybe I'll just do it when this lot are finished.

Sunday, August 09, 2009

Another Photo - Alexander Nevsky Cathedral - Tallinn


Alexander Nevsky Cathedral is a rather nice Orthodox Church right up the top of the hill in Tallinn. Tallinn is a lovely place spoiled only by us tourists :-) it was Sunday, there was a service going on and being quiet isn't too much to ask out of respect. Unfortunately a number of our European cousins on their tourist bus trips didn't think so. People can be pretty rude sometimes.
As you can probably see from the photos so far - we did get some pretty good weather overall.

Limbo State

Tomorrow is the pre-assessment and I can't say that I particularly like it. So familiar am I with the nurses there that I have a swab kit here to pre do some of the tests for MRSA so I just need to hand those in.

I suppose it can't be helped that I am a little heavier than the last time I went in. Other than that I will just have to see what tomorrow brings. Friday just needs to be over and done with and I hope that by this time next week I will be able to be sitting here writing some good things about the procedure - unlike last time.

To tell the truth I have now forgotten how many times I have actually been into Hospital for biopsies and TURBTs - I think this makes 7 times but I'd need to go and check that out.

I'm trying to be balanced and tell myself that I'd have settled for going in every 6 months for the rest of my life if they cured me - that would make me shudder but you can probably see that the act of reminding myself that the treatment has been life-saving brings some perspective back to the situation. I forget (like most people do) that through all the horrible things that have gone on the undeniable truth is that I am here still, I am in good health (although not great health) and that I need to count myself privileged to be in a position that the next operation is to check that things are OK not to remove tumours or anything else worse than that.

I've been quite down this past week and pretty downbeat, pessimistic almost (and many who know me would realise that isn't my usual state). Today I'm in a different mindset and I'm beginning to think things through more - rationalise it all out and make sense of what is going on. I did get a bit of a shock when I daydreamed of going to the woods and saw a picture of myself hanging from a noose on a tree - that snapped me out as well. I hasten to add, it (suicide) doesn't enter into the equation but it was a vivid representation of the depth of last week's depression. If you are wondering, I wouldn't because of what it does to those who know or knew you and those who found you and all that sort of stuff. I can understand why but not why you would upset loads of people by doing it (train jumpers for example - and I saw one just the once and it did upset me too). Yes, a daydream and a warning painting - the brain is a complex thing.

I have to face facts sometimes that I'm working with the cards I've been dealt and worrying about things beyond my control. Worrying doesn't change things but it is so much part of the territory (the Doctors don't tell you about) that I should be getting used to it by now. In some ways, maybe I am that I can work it through and know that it is transitory in nature. The whole Cancer trip is a fairground ride where someone has tampered with the rails or half sawn through the wooden supports of the roller coaster you're on. To your Doctor it is a tumour to be removed, treatment and checking and best care for a cure or remission. if it is worse then there is no doubt a protocol to follow in terms of whether they have time and ability to slow or stop metastasis. They have a matter of fact approach whereas you have to live with the dread of the boogie man coming back all the time. Someone likened it to Post Traumatic Stress Disorder and along with the massive fatigue that can also bring is the constant worry that something is about to happen to you. On a tour of duty service personnel have huge amounts of stress for long periods - whether they'll take a bullet, an IED or die, every hour or every day for the whole tour of duty. In Cancer it is that every twinge, anything out of the ordinary any slight change is a return of the cancer. There is always the worry that it will come back and that it will come back and get you next time. Your brain doesn't help you with this, it just adds fuel to that particular line of thought and makes things worse unless you spend time equalising out and in almost a right hand, left hand brain way think through the whole thing.

It is funny that last week wasn't "The Black Dog" I described earlier or even its puppy :-) It was just an uneasy state of being "stuck in a rut" or if "I hadn't got cancer?" or perhaps a bit of the old self-pity or the down after the holiday and returning to work. Who knows. Cancer just amplifies this and I it plays on your own fears and it magnifies them.

It is a nice sunny day outside, as usual it looks as if I am the only one in the house and so I will set up outside with a radio (Test Match is on) and a shade and have a relaxing day.

I do have my health and I have family, job and yada yada so I ought to be thankful that I have those.

Saturday, August 08, 2009

Another Photo - Our Cruise Ship


A nice enough Ship P&O Artemis. At 25 she shows some signs of age but is a bit like an old pair of worn in faded jeans - comfortable and familiar.

Friday, August 07, 2009

I thought I could take photos

We did the family photos - not mine just A's and L's photos. They both had a great time and L's shots of Argentina are amazing. A's Venice and Rome ones were also quite stunning. We didn't have time for mine but as my photos amount to theirs combined - over 1,800 photos and the best part of 2 hours video it would be a bit too much just for one sitting. Tomorrow maybe.

Kind of dreading this time next week - I'll no doubt be stuck in Hospital overnight - I do hope though that this time it is in the Urology ward where they actually know how to look after you!

TGIF

Just got home and will be spending quality time (as they say) with L to hear her stories of Argentina, Paraguay and Brazil. I just glimpsed some of the photos and it looks to have been a brilliant trip.

Work was a bit hectic. The Boss's one day back and everyone wanted a piece of him. I got in early but he is off for 3 weeks to Canada. I have my own worries with the pre-assess on Monday and the operation this time next week. I don't feel good about this one at all and I think that I've already touched on why that should be.

Anyway, at least I can look forward to a warm weekend so they say and perhaps we can get the barbecue out and we might even drag my screen and projector outside and have an open air movie of our holiday slides and videos :-)

Thursday, August 06, 2009

Plane has arrived at Heathrow

Just waiting to get the call and I will order the take away Chinese which L has ordered along with being me with a Yorkie Bar (a large UK chocolate bar advertised as "not for girls").

I got home a bit early and have set up the kitchen ready and am tracking the flight. Very much looking forward to seeing her as it has to be the longest time apart any of us have ever had.

Wednesday, August 05, 2009

L comes back from Argentina

In about 18 hours time. I am really looking forward to seeing her. I do miss her - she is so funny and so "off the wall" - I don't know where she gets it from.

I'm so proud/pleased etc. I just want to hear about everything she has done and to reinforce in her mind that she did this almost entirely herself - she raised almost every penny/cent and I am hoping that it will be a real life changing experience for her. We will have a big party tomorrow night and unfortunately I need to be in work the next day as it is the only day the boss is in!

I imagine she will sleep the whole of Friday anyway and so we can have a great family weekend and just listen to her adventures.

Nice night out

At the Jazz evening. Been going since 1988 so a bit of an old hand. I'm still the youngest one there though :-)

Feeling kind of maudling at the moment and just not my normal happy go lucky self. Sure it will change once all the crap is out of the way.

Guess what? My PC which was terminal I thought - is back with me and working. How cool is that? The PC man tested everything and it all worked, which is biz are as when I did that everything was dead. Anyway, glad to have that back and my car which cost a king's ransom to sort out this time. I suppose at 6 years old it needed all it brakes, tyres and bushes sorted. It is now looking like a real cat as it sits glistening on my driveway - Grrrrr!

Well there's your problem

On the way in to work it struck me that I really quite resent having my life changed and it adds to some of the reasons I'm currently unhappy.

Before BC I was on 4 times the money and every day was a challenge; I had responsibility and autonomy and status. Now I don't have any of those or, perhaps it is more accurate to say, I don't realise if I have any of those. I think I might have respect/status but the problem with taking a job lower down the food chain is that it doesn't push or challenge and it has now got to be routine - which I think is a better word than mundane. I easily exceed expectations as expectations are set for someone at the beginning of their career, not with a 1,000 year's knowledge and experience like me :-)

Getting up and going to work is mechanical and not exciting although I enjoy the people. It is funny that I'm feeling this at a time when, if everything is clear, I will be able to negotiate a permanent role. I suppose in this day and age having a permanent job can be looked on as a good thing.

Anyway, so I've pinned down one of my current issues. I know the other one is just reeling from having to go in for full biopsies again and realising that I will have to continue this sort of thing for whole of life, it isn't going away - or isn't likely to in the next several years.

Perhaps there is also the uncertainty about what they'll find - it has been 8 months since the last operation and I've had no maintenance since that time...

A combination of things then but it is all about coming back to the reality of what you have - a manageable acute disease that can recur when you least expect it.

Tuesday, August 04, 2009

Occasional Images of the holiday

CLICK on the image to make it much larger.

Why not I thought put a few images up. this one is pretty damn spooky. In Copenhagen we looked over by a bridge and saw these statues staring out of the water at us. I hope you can see them - oh for a filter to be at hand but, of course, A has all my lenses and filters :-)

Doom and Gloom Mood continues

Actually it was lightened a little as some more of my colleagues were in today and so that lightened me up a bit. I realised that I didn't actually tell them that I was due in next week - I'll tell them tomorrow.

We are getting ready for L to return on Thursday night. My car got serviced today and at close to £1K for the work needed I might need to start thinking about my little luxury :-) however, Mrs. F. is going off to Heathrow on Thursday to pick her and her friend up so there will be a massive welcome home for her then. I have to go to work on Friday which is a nuisance but I reckon L will sleep for 24 hours anyway so we have the whole weekend.

I can't say that I am looking forward to the next few weeks. Perhaps it may be the last invasive work on me, perhaps it wont, we will have to wait and see the results.

there was a series of programmes on last night about Cancer - very interesting and I'm getting my head back around the fact that as ordinary as I appear and as much as I'd like this all to go away, it isn't going away and it will come back at decreasing frequencies (I hope) for the rest of my life.

You don't really understand that as you hope that you'll just get discharged and that will be it. It may be with some cancers but not, it seems, with bladder cancer at the level I had anyway.

I'll see if I lighten up a bit more tomorrow. At least it is Jazz night tomorrow and I will enjoy going to that and spending some time with my friends.

Funny mood

I've been in a funny old mood for a couple of days now. I'm not sure I understand all the reasons why - I can guess that it is a combination of things and I'm sure it is coming back to "routine" and I really don't do routine at all well. I couldn't hack a job that was the same day in and day out. This job has got a bit "samey" now and I suppose from being someone that had to walk into everyday and tackle whatever turned up, this can get quite dreary and like walking through treacle to get something done that, frankly, should only take a few hours.

I'm neither one thing or the other at the moment and it isn't depression although it is close, it is perhaps coming back to normality and the day to day trudge of life. Things just go on much the same everyday and it would be nice for it to be different occasionally.

Monday, August 03, 2009

No one likes an Operation

Least of all me. Not my usual cheery self today at all at work. Was a bit grumpy and a bit annoyed with just about everything really. Annoyed with the stuff left on my desk; annoyed that I feel not so great about my holiday and annoyed that I have to go in for a full blown operation and the needles and the other baggage that goes with the territory. I can see how some people just give up and finally refuse treatments and so on.


Interestingly enough, I just haven't convinced myself this time that this is necessary. I thought that the December Operation was it and that all would be over and every time something happened to me, I convinced myself that it would be the last time that I needed to have a cannula in my hand, go to theatre, wake up from a strange sleep, argue with the nurses about my inability to walk around a ward when I was connected to the bed and all the other "fun" things that happened to me last time. At each stage, it was my defence mechanism. This is the last time you'll need to do this or that I'd tell myself.


Obviously not then!


Oh well, I'm tired and I need to get some sleep. A has heard from L that she is alright and relaxing back in Buenos Aires ready to come home later this week. Goodness she has been away a whole month.


Talking to A tonight was interesting, it appears that she was one of only a very few who got Distinction in her exam. Some only got passes and there were very few merits awarded either. She really does work very hard and just looking at her notes and research you can see how much effort went into the project at the end. Good on her. It looks as if she has got her place secured and will travel up from here every day. Good on her I say.

Sunday, August 02, 2009

The wake up call

The brain is great at forgetting things and also I have that sort of personality that throws bad experiences away and moves on. Enough sh1t happens that you need to dump it and move on. I'm relatively lucky to be able to do that and once it has happened and is over and the short term disappointment or whatever other experience I had is thrown away and only referred to when needed.

I'm just feeling a bit down at the moment as I know what is coming and I just need to get over this phase which looks at the downsides of what is coming. The upside should be that the results will prove where we go next. The positive side could be that this will be the last operation and that I'll go onto the challenging but probably better flexible cystoscopy...

In the overall scheme of things, I just have to go through this operation and then see what happens next. I forget, or I quickly forget, the fact that I have had a very serious condition and this is the territory. This is all for my own good but it still isn't great and it isn't something you'd choose to do.

So there you go - it is, I suppose, the shock of coming back off of holiday and finding the letter there telling you when you are going to get done.

Feeling quite low

Probably as a result of coming back from holiday, realising that the operation is less than 2 weeks away and remembering the mess I was in last time. Then there is the perennial "what am I doing?" question coming along. I'm back on my mid life crisis stuff. You know the sort of thing, "surely there is something I should be doing?" "Why am I not happy with things the way they are?" There just seems to be a cycle to this which at the moment finds me in depressed mood. I'm also going through the everything is cancer phase again. There is a small swelling in my mouth, some of my moles look dark, I had a bit of a cough the other day, my throat feels dry. Everyone of them is cancer but probably aren't. You just react to every little thing like that and yet I'm in good enough health really. I think it is just a phase again and the pattern is much like this as I get highs and lows all the time.

I don't consider myself to be a hypochondriac but just recently I've been given to this train of thought. Of course it is now well over 3 years since the first operation and my goodness how time has flown and how things have progressed on since then. I had the funniest moment on the ship when someone mentioned getting off at Tallinn and visiting the cigar bar. I almost felt like going along and sitting there and lighting one up as if to defy the cancer gods and sneer at them. What a bizarre thought.

I do hope I snap out of my current malaise. I really don't care to want to go to work or do anything at the moment and when I'm like this I am at my most destructive as I don't tend to do what I'm good at and that is think logically and measure my thoughts and actions. I am likely to go and do something stupid like quit my job or bark at someone.

Off to bed now and hope to shake this apathy for tomorrow.

Saturday, August 01, 2009

Tired from all that walking

For the second day we have laid in and got up late. No problems with that - but pretty much as we felt that the holiday was going to be quite exhausting even though they missed two ports. I note that they also managed to do that on the previous cruise too. Some can't be helped due to the weather but a mechanical breakdown meant that in reality out holiday didn't actually have an end point and so was left in limbo. Unfortunately the people at P&O don't have that sort of mindset and the poor old Captain was left without much to calm down the passengers.

Some of the dyed in the wool types who actually haven't been on any other holiday or with any other company thought this was a reasonable stance - we missing 25% of the ports we were expecting to see didn't. Some poor soul was actually due to get off at Gothenburg but ended up trapped on the ship like we were. Mind you at least they were compensated properly and were able to fly back there. We had hardly enough compensation to get us to the airport. I still await a response to my complaint that I made on board. However, given their inability to inform us of anything in a half decent manner I'm not holding my breath on that.

It makes it sound like a bad experience which it wasn't really but we were amazed that they were so unprepared for something that appears to happen quite regularly with P&O. It was that their customer service and communication stank. I thought their strap line "Everyday is different" was a load of bollocks especially when stuck on the ship for 2 days longer than you planned to be as everyday was "the same".

I can't say that I am particularly looking forward to getting back to work on Monday or to getting myself prepared for the next lot of biopsies given the awful experience I had last time. I think I'll make the point this time when I go and see the pre-assessment people.

Friday, July 31, 2009

For pity sake now the other PC

My rather swish notebook PC has died. Typical and lucky I didn't destroy the photos on my camera after I downloaded them! The thing just expired which looks like an internal power supply fault. Of course it is out of warranty and of course it is the primary PC I use. Whilst it is backed up it isn't much use to me to transfer at the moment as it uses a different operating system to everything else.

So a trip to my local store to see if they can rectify is in order. It is a damn nuisance of course as it is also the PC I use for presentations.

2 weeks today and I'll be in hospital getting my biopsies done. Please, please, please let it be the last operation I have to go through. I am beginning to loose count now of these. I can understand though that they need to do this. It is pretty aggressive and they want to make sure before going along the next route. With recurrence always a possibility I suppose I ought to also be prepared for that as a possibility - waking up with more troubles than I went in with.

The holiday already seems a long way back in the distance.

Thursday, July 30, 2009

Back Home

A great time but tinged with a few disappointments about the Ship but on balance we had a great time and we are still talking to each other. I'll get around to that later I'm sure but the other news is that I have the date for my operation - yes - full biopsies once again!

The problem with that is that I have managed, even with loads of walking almost everyday to put on a fair amount of weight. Oh well - it will be a challenge to see how much I can lose in a few weeks!

I've been well all the time we have been away and actually look like I have had holiday too as it was great weather unlike the UK which appears to have suffered a washout.

Just met up with A who also had a good time in Venice and Rome. L has sent a few messages saying all is OK in Argentina.

More when I get settled back home.

Thursday, July 16, 2009

Final Countdown Begins

I have my check list to fulfil including the need to go up to the shops and buy myself some reading glasses. I was repairing my spare set when Mrs. F. tried to be helpful and as I was searching out a pair of pliers she straightened one of the arms against the lens with the inevitable consequence of shattering my lens :-( As luck would have it, they are only £5 a pair reading glasses and so I'm not that upset and can wander up to the Chemist to get some more.

The cars are switched on the drive, I need to check tyre pressures, put out the rubbish, unload the dishwasher and a few other chores and then go and collect Mrs. F. from work and we can get going.

I'm looking forward to the break - the weather doesn't look great, lots of rain everywhere but let's hope that it picks up a bit for us. As ususl the BBC long range forecast of a blisteringly hot summer (the 3rd time in three years they've said it) is, like the previous years, proving to be a bit of a punt in the dark! If they say it long enough, one year they may get it right.

I'll sign off for a while unless i decide to visit the cyber cafe on board and hope everyone keeps well in the next few weeks.

Watch out Baltic here I come

Packed, just about ready and logistics are worked out so as we go A returns and this time tomorrow we will be well at sea and halfway to Norway.

I am really looking forward to this now - I really do need a break too as I am just so damn tired all the time. I have my check list ready for the morning and then I can go and pick up Mrs. F from work and we can get down to Southampton and get away.

I missed the work get together but I wouldn't have been much company as I got off early and still managed to fall asleep on the train.

I've even managed to transfer my e-mails so I can (in theory) get them on the Ship if I wanted. Not sure I do but there you go.

AndyP dropped me a line and he is doing fine which is great news. I haven't contacted the Hospital, I will do so on my return though to find out when they want me in. August is good as nothing is happening but my diary for September is getting full up already!

Tuesday, July 14, 2009

What is it all about?

Out tonight with old school chums - good laugh, a few beers and life is great. I wasn't on top form but close. Holiday is so near I can taste it and I am really keyed up to go now. L has contacted us from Argentina and is having the time of her life - - oh for the opportunity when I was younger to have done that trip - she really is enjoying some down to earth experiences. Best one - she washed her knickers, hung them out overnight to find a minus 10 C had frozen them by the morning - great stuff and so many anecdotes for later - I envy her but I am SO proud of her achievement - she has worked so hard for it and deserves to go for the effort alone. I've been a bit hard on her as I have made her work for the whole thing but, nasty piece of work I am, I think that if you work for it and it is all your effort then you appreciate it so much more than just us paying for her to go.

It is still strange not having either of the girls at home but reassuring that they are independent and confident travellers at just 15 and 19 years old.

A has secured her Distinction in her Art Foundation and her place at University is now assured. She is pleased. I am also delighted for her. The examiner's remarks concur with my view that she has put a massive amount of effort into her work and the subtly of her work is way beyond her years. I always thought that our family were good in terms of artistic skills - I could be good if I practised and turned my attention to it. A's work is stunning and when I saw it recently (through the pain of the cost of the reproduction photos) it stood out as an excellent work of photographic art. I feel as if she is so many years in advance of me. I am a keen amateur and I can take the same photo as A but you would look at mine and say what a nice photo and look at hers and ask "what is around the corner or off frame?" Such is her eye for composition.

I kind of look at things and wonder if "my work here is done?" Both girls are ready to go onto whatever their career path holds for them and now, it is beyond my level of expertise and knowledge. My background being useful as a first from the University of Life can probably only give sound advice. theory and usefulness to even comprehend their chosen subjects is now beyond my ability to help.

Monday, July 13, 2009

Blogging at work

Surely the slippery slope here David?

Well, to tell the truth things are a bit slow here at the moment. The bottlenecks are often those I work for and until they release a piece of work back to me after review or unblock a road block for me, I can't get on. What I have done today has been accomplished and it is the middle of the afternoon and I could easily fall asleep or just go home and still get as much work done.

The tiredness continues to bug me though and not being active makes it worse somehow. It isn't anywhere as bad as it has been but even so I find it annoying that it still happens.

Oh well only two more days at work and I can get off and enjoy a break.

Sunday, July 12, 2009

Planning and anticipation

I am looking forward to finalising holiday arrangements and after clearing up the last of my "to do" list this morning I watched the German GP and then got down to some serious research as I really haven't gone into details on a couple of the cities - Gothenburg and Helsinki figuring that I have time to do that especially on board as there are plenty of briefing sessions to attend.

No word from the Hospital still - I suppose there is still time but the NHS is struggling with Swine Flu. Someone in the village has it apparently. They are talking about suspending all routine and non essential operations to deal with the "pandemic" - yeah right.

Oh well - just another 3 days at work and we can zip off to our Baltic Cruise and two bits of trivia which I'm not sure I really wanted to know are that our Ship is about the size of ...........



The Titanic



The better news is that Cruising is statistically the safest holiday type :-) - unless you happen to be off the Somali coast that is I guess.

Saturday, July 11, 2009

Food still here, less washing it can only mean

The kids aren't here. The house is less crazy, much larger, the milk and Fridge don't mysteriously run short at a moments notice, the toilet paper is always available in the bathroom and the bathroom is always free. No one asks for anything and the sound of (what I swear are Wildebeest) running up and down the stairs, slamming doors and other associated din has gone.

It takes some getting used to but it is rather pleasant actually :-)

Another 3 weeks of this - bring it on!!!

Thursday, July 09, 2009

Interesting Evening

Topped off by bumping into my neighbour (cured of Lung Cancer) and discussing our cases at 11:30 at night both on the way home from nights at the pub.

Interestingly I was with 3 young ladies from work and had an evening of bizarre revelations and interesting anecdotes about work. I am an INTJ I don't get a lot of this - I just want to wade in and make it work. The fun is coming soon anyway when I negotiate my hours and my rate. They want to pay me less than one of the PAs and most of the other staff as the job has never been "valued". I shall enjoy myself when I get back from my Holidays.

A part time day tomorrow - looking forward to it and to discussing some things in sober light of day!!

Wednesday, July 08, 2009

Not good today either

My stomach wasn't great yesterday and this morning I woke up really tired and decided not to go to work.  I ended up with an extra 5 hours in bed and feel a bit better now.

All seems well - planes have landed where they have meant to land and no news is good news.  I completely missed the date yesterday - one of my milestones - the day I went to see my Doctor who pronounced matter of factly that it was probably a tumour that I had and then told me they would knock me out but they did a flexible Cystoscope under local anaesthetic.  

I was pretty traumatised at that point and was in a right state when I got back home.  All I remember was starting to smoke - which I hadn't for ages and drink and generally feel pretty sorry for myself.  That lasted about 2 days then I moved on a bit but to think that it was 3 years ago surprises me - it certainly doesn't feel that way.  Of course the 7th July also hails the anniversary of the London Bombings and I remember being caught up in all of that.

I'm away for the 21st and 25th (diagnosis and first operation) I'm in Visby and ST. Petersburg respectively and I never thought I would be.  What will be good is that I have kept my own promise to myself to do some travelling and enjoy myself and celebrate being alive.  I'm really looking forward to it now, so much to see and do.

Tuesday, July 07, 2009

Strange day

I've actually not been great today, having some stomach problems. I'm certain it is the pub I took refuge in last night from the rain. It seems to be something to do with that pub - I'm sure I got something similar last time I went.

Went off to see L off. She was very upset and in tears. Not because she was going but because Mrs. F. hadn't turned up and everyone else had and they had been asked to get onto the coach. As luck would have it Mrs. F. turned up at that moment and so things were OK. There were many tears and I really didn't like it at all. As I've said before, these sorts of things really turn me over just because of how emotional it all is. It was never a problem with me before BC. These days I do find it disturbing. Anyway, all went off alright and she was laughing and joking as they drove off which is more like her really.

They've had a slight delay but have a long hard journey ahead of them. She is off to Madrid as I write and then flies to Buenos Aries later in the early hours of the morning. An overnight stop and then a 24 hour bus ride!!! I'm sure that she will be fine once she gets there.

That's the second one gone

Just driven off for final briefing. We are going up to the school to wave her goodbye but that is both A and L off of our hands for a while. It is spooky that we wont see them for almost a month each.

I'm looking forward to waving L off though, she has worked so hard for this trip and raised all the money herself whether that be sponsorship or actually working for it. It will mean a lot to have achieved that and I'm sure she will come back a changed girl. Funny thing that she is (she has my sense of the surreal), she had a T-Shirt made up with "Argentina 2009" on the front and "Fernandino" on the back because no one can spell our surname! Good on her, with that sort of attitude I am sure she will thoroughly enjoy her expedition.

The house is quiet now - spooky, I bet the food lasts longer too :-)

I'm looking forward to my holiday too - not long to go now and I can actually get some time to sort out the visits for all the stops after St. Petersburg which has taken priority whilst I arranged private tour guide and driver to get away from the madding crowd and to save a huge amount at the same time.

Monday, July 06, 2009

Day off

I decided to take the day off tomorrow. A good move by the looks of the chaos that is the house this evening. I just let them get on with their small tantrums and by this time tomorrow it will all be over and I'll be staring at Mrs. F. and wondering quite what to say after 19 years of having one or other of the kids or someone else's kids in the house. Spooky!

I will go and wave L off tomorrow and I'll try and be up to wave off A and her boyfriend. I'm pleased that they are getting out and about and exploring the world and doing it themselves. I'm glad I am still around to see it (of course) as I never did think I would be.

Once they have disappeared Mrs. F and I can get down to sorting out our own holiday.

Some massive rain showers around this evening - I got caught in two of them - luckily I was picked up part way home or else I'd have been soaked through even with an umbrella.

Still noticing the tiredness - probably the weather too not helping.

Ready to move on

Disappointment lasted all of about 30 minutes yesterday. I had kind of resigned myself to knowing that it was a stitch up after I spoke to some guys last Monday about it. What is annoying is the way it was handled and when someone says you didn't get to the next stage, they aren't actually telling you why. It would amaze me if anyone had more experience in a couple of the areas they asked for as those who do have more than me didn't go for the job.

So - plan A kicks in and I need to decide what to do here at work. The money is pants but the people are good. The trouble is that right now, the work is slowed up for the holiday period and so things aren't flat out. Maybe I should take that as a good thing? At least I have a few weeks to think it through.

Which reminds me. I had better talk to the Hospital about what they want me to do now?

Sunday, July 05, 2009

So it was a stitch up

I got the e-mail that had gone to my Spam box as it didn't come from where I sent the original. It was very short, non transparent and hardly explained why I wasn't considered.

Interestingly enough, as I understand it, they had an incumbent and had to advertise the post. It will be interesting to see who it turns out to be as I can't think of anyone with the same level of internal experience as I have but there you go.

I'm a bit annoyed that they wrote such a sh1t letter back and it was so poorly handled that I hope the new chap actually does something about the process. A few words of explanation would have gone a long way to smooth things out. The way this is done just arouses suspicions and gets hackles up.

Other than that the week has been very busy but I have been struggling with tiredness. Birthday was good, very enjoyable and today was a quiet day watching Wimbledon and recovering.

The weather looks set to break tomorrow - thank goodness as the hot nights were getting to be a bit much.

L is off to Argentina on Tuesday and A is off to Italy. Things are going to get weird around here after Tuesday :-)

Thursday, July 02, 2009

3 years in

Hardly seems that it is possible that it has been 3 years since it all kicked off.

Hardly a day has gone by when I haven't thought about my health since then. Things are getting better now as the memories fade and the traumatic times and the stress subside into the subconscious.

I'd like to think that this is it. No more for me thank you. But that isn't the case and I'll soon be back for either an operation or flexible cystoscopy to see how I am getting on. Not having the Treatment has been good and whilst I still get tired, it is nowhere near as bad as before. Now I can control it and go home early or fall asleep on the train. You adapt and move on.

There are other health issues but they are just things that getting old throws at you. I can't say I feel 100% fit but neither am I needing constant supervision and running to the doctors.

Things are OK at the moment. The collateral damage is limited to my immediate family and most of my spooked friends are back and able to talk to me. The job is good but not stretching and whilst it was the right thing to do last year, I wonder how long I can live within my capabilities and within the scope of my ambition?

So - life is rosy really, I don't have the dreaded Bladder Cancer - haven't really for getting close to 2 years and 9 months I guess. I'm feeling good and in reasonable health, I have a job that I like, that I am good at (although it doesn't challenge me), the kids are OK and my holiday is coming up soon. All in all - that is so much better than I guessed my outlook was just three years ago. I didn't realise exactly what I had at that time but I knew it was serious. Within a week it was dawning on me what I had and within three weeks I was diagnosed. A few days after that, I had the operation and my roller coaster journey really got going.

Have I changed? You better believe it I have. Goodness, what a difference in my outlook, the way I take care of myself, the way I treat other people and the way I see my life from now on. Apart from the quite strange "certainty" that goes with what I say and do now and how I talk to people, most of that I am comfortable with. I find my brain sharp as ever now in analysing business problems and coming up with plans etc. But the flip side is losing some of my well-organised side - it is as if the ordered side of my brain has surrendered that so that I can be more creative.

I am off out soon for lunch and hopefully will be able to just forget about everything.

Wednesday, July 01, 2009

Eve of the 3rd Anniversary

Crikey - we have been having a heatwave and I've not felt like doing much and the fatigue that this hot and humid weather - in a country that doesn't really have A/C is getting to me. Home early as I was so tired today and I am off out. Have been out every day and night this week and that goes on until Friday night.

Saturday - my birthday - Independence Day - will be one of flaking out and resting I reckon. People in my place are just plain crazy and still wearing suits and ties!

It appears that this other job may after all be a stitch up and someone has already been chosen. I think though, that the lack of correspondence and feedback is pretty bad. I know they have read my messages but even now they don't respond. I will be talking to a couple of people about it tonight and Friday and see what the situation is. If it is a stitch up then I imagine things will get a little ugly.

Tomorrow is the 3rd Anniversary of the presentation of my symptoms. Not official diagnosis day. However, it is a significant milestone for me and I am out at a lunch (how hot is THAT going to be I wonder? I shall be thinking about the onset of this which happened about 5 pm that day as I recall.

Still no news from the Hospital and I am happy enough to go on Holiday and then come back for whatever they are going to do to me. Whether it is a GA full biopsies or a peek and a poke.

I feel fine if not very tired and still somewhat overweight although if the weather carries on like this I will probably lose loads as I hardly eat in this sort of temperatures or what I do eat is normally salad.

I'd better go and get ready! A suit in this weather - what am I thinking!!

Saturday, June 27, 2009

Paint Ball

Well - what can I say - we enjoyed our day but the temperature was in the high 27 C and humidity about 50% and so I struggled. All these youngsters off running around and shooting me :-)

However, the good thing was that we had a really great day out and even I enjoyed myself. I had some worry though as I felt some chest and arm twinges. I think I will take myself off to the Doc and see what he says about those. I've had these minor aches before but this felt a bit strange. It wore off after 3 or 4 minutes but even so - if it was just that I am unfit or something more to worry about I ought to get it checked out I suppose.

A great day - now off to have a shower and try and sleep in high humidity and high temperatures. we don't do A/C in our houses much in the UK - we do in our cars (which WAS a welcome relief) and so it could be a muggy night.

Friday, June 26, 2009

Damn cold

Has kept me off work - I was going in but when I woke up I felt pretty dreadful and don't feel a bundle of joy and charm right now.

What with the strange text messages I was getting, it came clear and as a bit of a shock to see that MJ had died. All that money and fame can't help you when the time comes can it?

We are getting very close now to my 3rd Anniversary which will be next Thursday 2nd July. It was three years ago that the symptoms really presented themselves. Having said that there were a few minor warning signs before then but, it was the 2nd July that all hell broke loose and this journey really kicked off.

I think that I will have to do a reflective either that day or shortly afterwards to explain what the last three years have actually meant and the journey to where I am now. This year I will be out for a meal during the day and so I may spend a bit of time having a few beers afterwards. Don't know about that yet...

Thursday, June 25, 2009

If at first you don't suceed

Use alcohol and plenty of it.

Not sure if it actually has done the trick but came home early and had a couple of beers and feel a lot better. I could have done without the sneezing though.

I should be OK again in the morning and I am really hoping that the weekend goes well. I have never been paint balling but everyone tells me it is a good day out. I hope so.

Wednesday, June 24, 2009

It had better not be Swine Flu

I got up this morning and didn't feel great - then I got a cramp which really started off my day nicely :-)

I had to do my presentation which went down very well apparently and on the way back I wasn't feeling great. I got home, got changed and still don't feel really chipper. I've got very mild Flu symptoms so off to bed early and some lemsip and hopefully I'll be good in the morning. I don't need another dose of what I had at Christmas.

We are meant to be off paint balling on Saturday and so I hope that I am alright for that.

Let's see what a night's rest will do for me. Typical - I bet it was the sniffling woman who sat next to me on Monday on the train!

Tuesday, June 23, 2009

Getting on with life

Is sort of OK. It seems to be more normal to manage to last the whole week even though I am still tired and to get along without too much to worry about. There really is little to remind me that I was ill apart from I'm still somewhat overweight and the tiredness of course.

Tomorrow we are off to Slough for the AGM of the charity which will be nice as I am being driven there and back. As usual this afternoon was chaos making sure everything was there and that our speeches were all OK. I thought it was quite funny and my speech got altered again today and not by me and I'm delivering it :-) Oh well. It should be fun.

Looking forward to having an acting part as last time I was just the admin clerk.

At least I'll get a few extra hours in bed in the morning.

Sunday, June 21, 2009

Father's Day

I don't need too much of an excuse to sit on my butt for most of the day. Today there was the F1 Grand Prix and it was Father's Day so a good enough reason. Some beers, watching the Grand Prix and falling asleep afterwards :-)

It's the European Athletics, US Golf and 20/20 cricket all going on there are plenty of distractions. I've been doing some more background work on the potential new job. Working on my pitch and making sure that I have all the requirements lined up and an answer to each of the role and candidate sections. The more I think about it - the more I like the idea of this job. The challenge alone makes it worth going for. To actually get the job would be really interesting and might make a few eyebrows rise. In fact, that would be a bonus in its own right to see what the reaction would be.

Saturday, June 20, 2009

Deadline

The job deadline was Friday evening and I am hoping that I will at least get a chance to meet the team and have an interview. Of those who I know are also going for the job, I'm by far the youngest and also the one with the most recent and relevant business experience.

I suppose I ought to try and keep a level head. Id really enjoy the job and it would be something I could really get to grips with. It would fulfil an ambition long held and would really stretch me. I have tried to do the 9 to 5 that everyone recommends but it can get a bit boring.

Oh well, let's see what happens.

The Phoney War

It was called when troops sat out opposing each other for months on end whilst nothing actually happened.

Here I am, 6 months since the last invasive procedure and about 5 months since I was told I needed treatment and 4 months since I was told I didn't need treatment!

Gradually, life has returned to "normal". It isn't exactly "normal" yet as I still don't think that my family have come to terms with the fact I lived and I probably cannot get used to their subtle but very noticeable reaction to me. It isn't bad as such but I can't say things have returned to normal that way I still feel very different to the way I was and I'm sure that as my attitude has changed so the ability to adapt to my "take on life" must have changed massively.

I'm neither fish nor fowl at the moment. Neither ill or cured, neither well or not well. In limbo. I am making the most of being well though and that is the great thing.

We went out for a curry night this evening. We all had a great time and I have to say, the company was great and the food was excellent and suddenly, life is really worth living and your friends just grow more on you every time you hold an event like this. I hope we can fit in a few more this year - it really was an enjoyable evening.

Thursday, June 18, 2009

Longer between posts

Means I am a busy chap and also that I have been concentrating on other stuff too.

It is interesting that I still haven't heard from the Hospital. I won't be forcing the issue until I get back from my holiday and the tickets arrived yesterday which has got me excited. L has finished school and gets ready for her 4 week expedition to Argentina. A is set to go to Rome and Venice.

I'm working out, after 19 years of not having exclusive access to Mrs. F. quite what we are going to talk about for 2 weeks.

The closing date for the "other job" was extended to tomorrow. I won't hear much until next week I guess. I am on parade on Wednesday delivering one of the key speeches at our Annual General Meeting. It is quite an interesting one too all about our new Mission Statement and the new ways we are tackling child poverty. The slide deck I have produced looks good and I hope with a bit more effort tomorrow it will be really polished.

Tomorrow night we have our curry night. Lots of us. My Nephew is driving over from Luxembourg to be with us and so I am looking forward to a good evening out and then it is the British Grand Prix over the weekend plus the golf and all sorts going on. I have a lot of computer based work to get through as well this weekend.

I feel well, I feel fit and I'm hoping that I get an opportunity of this job. It would be a lot more than I am doing now but it would just be so enjoyable too. I'm also beginning to wonder if I might get a flexible cystoscopy this time given the fact that I have had no treatment and they only had the slightest issue with the cells last time?

Tuesday, June 16, 2009

Life after Cancer

It may seem strange but I get a feeling that those of us who have gone through the stages and are blessed with clear pathology have worked out that you can now get on with life. The threat which isn't really far from removed, is nonetheless, a threat now and coming to terms with the chronic side of our diagnosis means that we are mindful and wary but must get on with our daily lives. It is an unfortunate fact that we probably still have to work and go through the day - to day existence to make a living and that having lived through the yukky bit we now need to move on.

I never thought I'd say it but I am back to an almost normals state of existence but with a few very keen extras to my persona added on. "No one died" is my mantra these days. Today, some trivial, minutiae transpired at work and frankly all that was needed was to bang a few heads together. "no one died" - they look at me funny when I say it :-)

Life is as back to normal now as I can make it. There are still hurdles to get through and things to be overcome but watch out life, here I come again.....

Monday, June 15, 2009

Tiredness

I have noticed that I am getting better at managing being tired and it is possible for me to snatch some sleep on the train into and out of work. Just enough to charge my batteries. I also grab a few moments at home if I can. I still get tired, the exertions of the weekend really did take it out of me. I am out at least two nights this week as well and I have yet to hear what the arrangements are for this job I applied for as I notice that the date has been extended to this Friday when originally it was last Friday.

It is an interesting job to go for and it will be interesting to see what process they go through from here. I'm not certain whether they will want someone of my particular skill set but I see advantages in me having quite rare skills to bring to the party.

I must arrange for my biopsies as well during the summer when all is quiet at work. Almost everything is finished and next week we have the AGM which sort of closes down our season's efforts.

Still feeling good and getting on with things. Wondering whether they have forgotten me :-)

Sunday, June 14, 2009

Off again in a few minutes

I got a call last night and I'm off out for a few beers at lunchtime with an old friend of mine. He is a member of one of my Lodges and lives alone so it is nice for him to get out and bend my ear about everything from cricket to politics. It is a lovely day here today so perhaps we can sit in the beer garden or some such thing.

Yesterday was a long and enjoyable day and looking back on it, as always, if you prepare yourself you can cover off most problems. There will still a few but the team coped well (they were mainly new) and I hope that it bodes well for the future of the Lodge. The chap that I may work for was there and as is only to be expected was in deep conversation with the members and so I only managed to say a few words to him and we gave a nod that sort of noted that my CV was in with him and he had seen it. It was a sort of audition and I hope I passed.

Friday, June 12, 2009

Almost done

Ready for tomorrow

It is always a nightmare as odd things happen and those odd things are exasperated because there suddenly appear many problems out of nowhere.

For example, there are three extra people to dine tomorrow but the guy who does the dining isn't back until late tonight and nothing can be done about that. Somehow we have to work it out on the day. That is one thing. Now what will happen is that maybe three or four people will fall out or realise they weren't booked in and all hell breaks lose but you just cannot plan or mitigate for this. Everyone thinks that it is just their little problem you are dealing with as an isolated incident - the trouble is there are lots of these all arriving in at the same sort of time and it just gives you a headache.

It was to have been my last meeting and I would have been free of all this turmoil. No such chance as I have to do another year and then can get a rest. So another three of these and perhaps then I can rest. My replacement is well known to me and will be able to pick this up without too much difficulty I reckon.

So all day has been knocking out lists and checking and re-checking stuff for tomorrow. I hope that it will all be alright on the night (or day) as the chap that may well be looking to interview me for that "other" job also happens to be at tomorrow's meeting. I need to be on good form as I it will be a public audition by the looks of it.

I need to be on top form then. No pressure there :-)

As for health - I am still feeling good and more interested in keeping my weight down than thinking about good old BC at the moment. I suppose you have to get try and think "normally" and I have done so much this week that it really has taken my mind off of things.

It has been a busy week

I have hardly had time to draw breath and spent most of the week out and working late and in meetings. Tomorrow (or later today) I am at home and working here ready for my final major Lodge meeting of the season. I will be glad when it is over it is a nightmare at the moment. Especially as hardly anyone is turning up and there are just so many gaps in the officers. So I imagine tomorrow will be busy.

It is the final day for submitting interest in this other job. I am thinking a lot about it and whether or not it is the right thing to do. I would dearly love the job and the chap who I'd work for is actually going to be at my meeting on Saturday.

Still no news of the biopsies - have they forgotten or what? Do I call or just put it back if it arrives. My holiday is now about 5 weeks away and I am going to get into holiday mode after this weekend I feel. I'm hopeful to hear something on the job front next week and I need to consider quite what steps I need to take to get into shape for the holiday. I must get my walking levels up even though I must do three or so miles a day now - I reckon that I should be trying to get a few 5 or 10 mile ones in if I am to do justice to all these wonderful cities we are going to visit.

Health wise - I continue to feel well if a little tired still. The fatigue kicks in often but it isn't debilitating like it used to be. I can get on a train - like tonight - and almost pass out listening to my music. I had a few minutes in my chair tonight as well. At least I get a lie on tomorrow. No more worrying spots of whatever it was and despite most things I am feeling well and fit. My brain is beginning to sharpen back to a point where I am beginning to be instantaneous with my wit now. Before I had to work at it. I wonder whether General Anaesthetic and the BCG has finally worn off?

Wednesday, June 10, 2009

Tired

Oh boy I am sooooo tired again. Today was my committee day and all went well and I got everything passed which was just great.

Then I had to meet a colleague and after getting home at the crack of goodness knows when last night (did I mention the bus!) I got 4 hours sleep and went careering headlong onto my meeting.

I am just home again now at 11 or so and I must get to bed and get to sleep.

All is well and work was OK but, in reality, the problems are only just starting to mount as things take on their new perspective. the potential new boss is around on Saturday - I need to be on best behaviour.

Bye for now!

Monday, June 08, 2009

Another health adventure

I had sciatica or whatever on Sunday which faded away. Waking this morning my old friend cramp got me in the other leg and I've been hobbling around. I just got another twinge in my calf muscle (and it is still twinging along). I wonder if my body is trying to tell me something?

I feel as well recently as I ever have and yet my body is conspiring to remind me that perhaps something isn't quite right. Work was - well a little boring today as I've actually done most things and got them ready and they are finished. The summer recess is coming and after this Wednesday the whole place goes quiet for 3 months or so.

Luckily I will be out with some friends tomorrow afternoon and evening and so I am looking forward to that to break the boredom.

Nothing else to worry about - keeping my eye open for tell tale signs of blood in my urine but it must just have been a bit of thread or cotton or something.

Still no word on the operation and the biopsies. Maybe that isn't such a bad thing if I am going for this other job.

Sunday, June 07, 2009

Seems OK now.

It seems that it was all a false alarm and I'm not being complacent, I'll still be keeping my eyes open. It is amazing how quickly the fear of having a recurrence grips you and it isn't nice. I'd be pretty upset if that was to happen but I think I'd just have to be pragmatic about it.

I ended up this morning with what felt like a trapped nerve and could hardly walk or work. After a few hours - cold pack, ibuprofen and some volterol and things came back to manageable. I don't know if I slept strangely - perhaps I did.

I hope to hear this week about this other job I have applied for. I'd really like the job but I can see that there may be others better qualified to get it. It would be the challenge that I need to move on as I think I have moved on now. Gone is the need for a protective environment and I think I just need to take on a bit more responsibility.

Still no news on the Cystoscopy - there is always the next day or two or else it will be too late and it will have to wait until after my holiday - I don't fancy trying to do 5 cities in 6 days with a bladder that is wounded and needing to keep dashing to the toilet :-)

Saturday, June 06, 2009

Paranoia

I thought I saw something in my urine last night. I've been cautiously sitting down to go ever since and checking. Perhaps it was nothing. I am reminded that it is not far away from the anniversary of the presentation of my cancer. It started about now with a tiny show of blood in my urine and then went away. It was 2nd July 3 years ago (3 years - crumbs it doesn't seem like that) that it all kicked off in a big way.

3 Years and I've come along way since then. I can't be sure what last night's little thing was as, strangely enough, it could well have been a bit of fluff or bit of cotton thread and as I happened to be wearing red -perhaps it is that.

The trouble is you never seem to get away from these little worries and little scares. The thing is that it is a worry and must stay at the back of your mind. Lately, I have been doing really well and almost forgetting that I ever had BC or indeed that I am still being observed for it. In a way long may that continue.

I wonder if you ever really forget that you ever had this. I guess you must have the memory fade it out but it will always be there somewhere. I'm sort of worried and a little frightened too that it might come back. I don't know in what form and how I'd be able to take it if it did. It is probably best to just cross that road when you come to it but it is a niggle nonetheless.

Friday, June 05, 2009

The Smell of Cigarettes

Severely does my head in these days and somehow my clothes came home on Wednesday night stinking of smoke. Which is strange as I wasn't anywhere near anyone smoking all night. Perhaps it is because I haven't worn that suit in about 4 or more years? Strange. Then tonight I can smell smoke once again.

I can smell it now and whilst I knew people were going outside to smoke, it just seems to be lingering on or near me. Yuk

I used to smoke years ago and really dislike the smell of cigarettes. Cigars I can kind of live with but this smell of smoke on my clothes really is quite horrible as it churns me up. I think with aversion techniques and knowing what it did to me doesn't help...

Ho hum and still no letter. However a great night out at this Surrey Lodge. They sure know how to throw an evening meal - it was excellent.

Thursday, June 04, 2009

Sheepish Grins

There were some sore looking heads and bloodshot eyes there this morning. Strange woman didn't appear - I think I may have had some explaining to do if she had!

What a bizarre evening.

Onto the more mundane matters of where my appointment for my Cystoscopy is? So far, not a word and I'm wondering whether I should again take the initiative and drop them a line to remind them. I was sort of hoping that they would have let me know by now so I could plan things out. If it gets too late I will just have to postpone until after the holiday.

Feeling quite tired today and I have another heavy day tomorrow as I am off to Surbiton in the afternoon for a Lodge meeting. It is a bit of a drag but the food is always good there and it will set up the weekend nicely.

That WAS interesting

I am a compulsive people watcher and I love seeing people at their best and at their worst. Tonight was great. I enjoyed myself as I did my duty and worked hard to make sure that everyone who turned up, that I met, enjoyed their evening. I was host and escort and usher.

Afterwards, many were, well, enjoying the freedom that alcohol tends to bring. I was having a drink but certainly not anywhere near dropping off the radar and into the interesting area. I really do enjoy watching people when they are loosened up and can say anything they want. It was so interesting I stayed far too long and "encouraged" many to perhaps say too much or regret their involvement in the morning. I am going to enjoy meeting up with the people I was with this evening and see if they can remember any of the things they said to me.

I was discussing the merits of two people not smoking and they had been off for a few days and weeks and were trying to start again. I was SO surprised when they looked at me as if I should be dead when I told them why I stayed off the fags....

Just an interesting evening and if I must enjoy people watching I must also learn not to "bait" them as mercilessly as I did. After all with that much drink inside them, I am surprised they could think straight let alone actually talk!

Also adding a by - the - by here to see if anything comes of the young lady hanging off my arm for 30 minutes telling me how much of a Gentleman I was and how I had been very kind and considerate. Frankly it was a little embarrassing but there you go - funny nonetheless :-)

Tuesday, June 02, 2009

The deed is done

I sent off my CV and carefully crafted letter this evening and then dropped a note to the boss to let him know that my name is in the frame. I'm not certain whether they will go for me or not. I think I can really deliver on the job.

Of course not everyone would take that view as I might be a bit young for the job at the tender age of 52!

Tomorrow I get to do some volunteer work at Grand Lodge when the Duke of Kent comes in to give out cheques to a number of charities in the public eye to celebrate his being 40 years as Most Worshipful Grand Master. It will be a nice do and I am looking forward to doing some active work after being sat on my bum of r weeks knocking out the annual review. Which looks good I have now decided. Mind you someone is going to get a thick ear as they didn't even mention that just some anally retentive comment about one word in the whole document. Bloody jobsworth :-)

Best get off to bed now as a big day tomorrow.

Oh dear

It always happens - I just seem to attract late nights.

today has been good - I finally got sign off of my Annual Review (version 16!!!). I went to a meeting and have just got home!

Was out at a festival of music yesterday then off to a friend's wedding reception and so I am getting quite tired by now.

Wednesday HRH the Duke of Kent is attending Grand Lodge and I am working as a steward that night - looking forward to that. Still not absolutely sure about this new job but feel that I ought to toss my hat into the ring anyway.

No news from the Hospital. It should be imminent - in a way anything after the weekend of the 13th June is cool for me. But that week is the best and no later as it may affect my holiday and I don't fancy that.

I really could do with working out some sort of strategy to cope with the next few months but there are so many things happening that I'm not absolutely certain what is going on. I may just have to grip on and go for the ride.