Friday, 9 April 2010

rough week, rough day

I can't actually be bothered to write this blog, but there is news, so I may as well tell it. For the point of a blog is to tell news. It's my commitment to you. Be grateful.

The last chemo session - 3b - was horrible, as per usual. Lots more of lots more of the same. Especially vomit. Lots of vomit.

The main difference came when I would normally be coming out the other side and returning to work - the 'chemo sickness' feeling left around Tuesday as per usual, but my body continued to be very weak. So much so that despite hauling my skinny ass to work on Wednesday for a tokenistic appearance, I couldn't get the same skinny ass back to work on Thursday. I just felt very weak, even going for a short walk would leave me breathless ...

Christ, this is pathetic.You get the idea. Moan. Moan. Moan.

The actual 'news' is this - I've just returned from a double-visit-day at the hospital. First up was to tidy up my PICC line and snip down the length as it's slowly been coming out ... then it was back in the afternoon for my second CT spleen scan. You may remember that I had a CT scan way back at the start in December and if you haven't seen it, the image is on this blog here

I'm going to write more about this situation later on - but without giving too much away, I've seen the CT scan results, I've actually already got the CD with the images on (I've got good contacts!) and although I await my Consultants opinion next Wednesday, it's fair to say that we are not looking at a miracle here.

In fact, the size difference is pretty negligible - to these untrained eyes anyhow ... it's still a monster and I know this, as it's in my bloody body - I feel like someone has tucked a balloon stuffed full of Paxo under my left hand ribs. I haven't slept on my left hand side since November. So, the images have only confirmed what I already knew - it's changed - but it's we are probably talking about a 3-5% change here. Worth the last 4 months of shite? You can answer that.

So, if you are of the betting persuasion, then I suggest placing a large amount of money on the word 'spenectomy' being used in upcoming blogs.

So that's why I am so grumpy tonight then? No, actually. I can live with that. Or without that, as it will probably be. The reason I'm so grumpy this Friday night is because of my ridiculous anticipatory nausea issue. Somehow my mental mind and body decided that the aniseed flavoured water than I had to drink before the CT scan (about a litre, over the course of an hour, so things show up on the scan) must have been chemo related - and so now I'm back on my chemo couch, on a Friday night, feeling bloody nauseous again for no reason. I wouldn't mind, but I've had this exact procedure and drink before with no side effects, so I know it's another phantom sickness. I was looking forward to a night off - feeling a bit better - making some music, relaxing and now I know that the only way out of this feeling is to go to bed ...

Some days I want to just say OH FOR FUCKS SAKE, GIVE ME A FUCKING BREAK LORD.

Today is one of those days. So stop reading now if you are easily offende ...

.. ah.

Monday, 5 April 2010

it doesn't get any easier

"I'm sure you'll get used to it and it will get easier".

No, I won't.

No, it doesn't.

Chemo = Scouting For Girls.

Thursday, 1 April 2010

the most depressing thing in the world

... is a flat iPod, flashing its cheery dead-battery icon at me, when I'm in the Chemo Unit, resigned to the fact that I am now forced to, yet again, listen to the never ending conversations about bone marrow, blood, scrapes, urine and such like. I'd pay £20 for an iPod charger.

The good news is that thanks to Lorazepam, I don't feel so sick. I've had an xray this morning as they are concerned that my PICC line has come out to far ... Just waiting to see those results before the poisoning can start properly.

Bored. And music-less.


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Wednesday, 31 March 2010

facing the shit

OK, after my last trip to the Chemo Clinic (that resulted in nothing happening to me at all), my nausea went into overdrive, lasted all day and made me feel horrendous. You can imagine that I wasn't really looking forward to going back there today for a simple blood test and a clean up of the PICC line ... I'd convinced myself that stepping foot near that place was now enough to send me into a merry-go-round-at-sea-after-a-dodgy-curry type state.

I arrived, I walked through the doors - took the first hit of warm air that fills that place and gakked it down, face curling into a ball. Count to 3 ... 3,2,1 ... no nausea.

How odd. I had to wait the best part of an hour to been seen, then had about 30 mins of faffing - taking blood, cleaning the PICC line, you know, faffing ... but no nausea.

So I just don't get it ... clearly my brain knows the difference between 'about to be poisoned' and 'not about to be poisoned'.

The proof, I guess, will come tomorrow.

Tomorrow I will be poisoned.

--------------------------

I went to see my consultant after the above. She is in a different part of the hospital to the chemo unit.

We had a chat about a couple of things - the anticipatory nausea, the new Lorazepam, my impending codeine addition but the real reason I was there was so we could discuss my spleen theory - that being, that the spleen is not getting smaller and we are somewhat pissing into the wind trying to reduce it. I rephrased that last statement for her, because she's a bit posh, like.

I got half-naked, laid down on the couch and she had a feel of Mr.Spleenerooney whilst measuring him with a tape and was in agreement - it hasn't reduced in size.

A C.T. scan appointment is going to be made, so we can see for sure and my consultant is going to discuss my case with her peer group of Very Clever People, but she all but told me that her original hunch was - and still remains - that the spleen will have to be removed.

There's no point jumping the gun about that now - but that's how it's looking at the moment.

I am due for Chemo Session 3b tomorrow (they go 1a,1b,2a,2b,3a...) somewhat stupidly, I wrote in a previous blog some time ago that I was on 4a or something ... I miscalculated ... I've actually only had FIVE treatments so far. It seems like this has been going on for ages now, and I've only completed 5 treatments - Christ.

Well, number 6 (or 3b) is definitely on .. my white cell count is back up. So bang goes a nice 4 day weekend. No Easter break for me. Jesus hates me, as I suspected anyway. It's because I use his name in vain (see above paragraph).

Tonight I start back on the Lorazepam - half a pill at night, half in the morning - enough to whack me out for the impending poison-fest I must face. Lorazepam nice, chemo evil. It's a bit like smoking a nice relaxing spliff and being forced to watch a JLS concert.

I'm running out of words to describe how I feel about having treatment now. You try to remain as optimistic as you possibly can - hopeful that this time it might not be so bad.

But, let's face it, it's always shit. It's chemo. Chemo is shit and cancer is shit.

But sometimes in life, I guess you just gotta stand up, take a deep breath and deal with the shit.

And here endeth the blog.

Friday, 26 March 2010

nothing happened: conclusion

... Quick mobile update to follow from yesterdays drama piece.

I stayed up from 8:30pm to 12:15am and felt sick all the time. I went back to bed and slept OK, but had nightsweats and amazingly bizarre dreams.

As most days now, I wake aching as I've realise I've got a slight codeine addiction again, so a mild dose of that and I should be ready to return to work.

The phantom sickness has gone mostly. I'm sure it will return when people start talking to me about it.

Hence this, so they don't.

But some good news just in. DV247 (music shop) are couriering my long overdue Access Virus Ti2 Keyboard to my house tomorrow, so the weekend is definitely looking up.

Onwards ...

Sent from my BlackBerry® 9700 wireless device

Thursday, 25 March 2010

tramatic day: nothing happened

I've just about had the worst day I've had for a very long time. And nothing happened.

I turned up for chemo. The moment I walk into the unit, I feel sick. Really sick. I run to the toilets and they are occupied, so I run outside and start ... crying.

I haven't done much crying since all this happened. I used to cry a lot, but for some reason, I don't really cry about cancer. I cry about chemo though.

A nurse comes out and does the stroking the arm thing, encouraging me to let it out. Which I do. This is now officially the most amount I have cried about my situation. The timing is not idea.

I return to the unit. The sickness is stronger. Officially, it's called 'anticipatory nausea' and officially it is fucking nuts. My whole body is as sick as if I've had chemo. I need to keep a sick bowl by my bed as the nurse starts to take my blood from my PICC line.

I now have a wait - regular readers will know that my white blood cells are useless at regenerating themselves in 2 week and invariably I get sent home. Having low white cells is known as being neutrophenic. My blood is sent 'upstairs' for testing - the results take about 90 mins to come back and determine if I am 'well' enough to have chemo.

As I wait there, I am feel rougher and rougher. As you can see from my mobile rant earlier, the environment doesn't help. Sick. Sick. Sick.

I see another patient who started having treatment after me and is on his last treament today. He has had the same 'ABVD' drug treatment. Although he displayed little of my symptons at first, his experience of anticipatory nausea is starting to echo mine. He talks of the how looking at the blue NHS lunch boxes makes him sick and how each treatment is worse. Mercifully for him, his treatment has been relatively short and today should be the last. It would appear I'm walking a much longer road than him. I wish him well and hope, for his sake, I never see him again.

After an hour or so, I'm told the news. I am neutrophenic again and am being sent home. Another 5k of NHS chemo drugs to be poured down the plughole. That stuff doesn't keep. They sensibly realise that from now on, I'm to have my blood test the day before, so the drugs will only be ordered if I am able to take them. I reckon I've been responsible for about £20,000 worth of chemo wastage. If you're reading this in America, you'll now see how us Britian's could not understand your resistance to Obama's health reform. As flawed and cash starved as it can be, the NHS is a bloody miracle. You should be grateful you have a president who sees it the same way. I would be screwed right now, if it wasn't for the NHS.

Mental exercise: Imagine you have a mentally damanding test to do. You are nervous. Very anxious. You don't want to do it. Perhaps it involved some physical danger, like jumping off something high or getting into a bath with spiders - whatever freaks you out. You are full of fear. Full of anxiety. You feel slightly sick. At the last moment, just as your anxiety is at it's highest, you are told you don't have to do it. The anxiety drops, the fear dissapates and relief rushes in.

So I'm told I don't have to have chemo. But the sickness doesn't drop, doesn't dissipate, there's no relief. I'm still feeling very, very sick. Shortly after, the nurse detaches my line and flushes it with some saline. I grab my sick bowl and wretch furiously into it.

Finally I get to leave. To suck down some fresh air. That should help. It doesn't. I am still sick.

I have a plan. To eat. A dear friend takes me to a pub, where I have a vegetarian chilli with rice, followed by a huge piece of chocolate cake and icecream. The plan is to change my body chemistry, the smells, the tastes, the feelings - yet, although I enjoy the meal, as I walk back out into the carpark, I realise I'm still feeling sick,

So, I go home. I take a handful of anti-nausea tablets and go to bed. At 2:00pm. I fall asleep in a heartbeat and the next thing it is 8:30pm.

I still feel sick, but slightly better. As I write this, I feel sick.

I feel as sick as if I have had chemo.

The insanity of this situation is hugely apparent to me. Today, I went to a hospital, had some blood taken from me (didn't even need a needle, direct out of my PICC) and then I was sent home.

I feel like I've been through an emotional wringer. I never realised that anticipatory nausea could be so devastating. It's now 22:30 and I still feel ... sick.

I've been given some Lorazepam for next time, to take before I return to the unit, to help, to sedate. I pray that it does for this is getting out of control.

My spleen feels big, treatment is delayed again. Nothing is very great news and does lead me to the same conclusion, that, at this rate, in time I will in time be looking at a full splenectomy and all that goes with it.

We shall see .. but for now, I sign off still feeling sick, yet knowing that nothing has happened to me to make me feel this way.

Insanity. Pure, insanity.

New rule

People in cancer/transfusion units should be barred from talking about tumers, blood in urine, death, bleeding from nose, putrid boils and whatever other subject these sodding people seem fascinated with. I'm feeling really, really sick already with anticipatory nausea and your eternal conversation revolving around your fascination with internal organs and bodily fluids is pushing me to the point where I might barf on you, which will give you something to fucking talk about for the next three months.

I forgot my headphones.

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