Meningioma operation. And beyond

Note to readers: I am no expert in this stuff. Nothing in this blog should be taken as medical or psychological advice. In fact, I’m writing it in what is still realistically a post-operation haze, so my opinions are probably coloured accordingly. I have gone from diagnosis to operation to recovery in a little over a week, so my impressions are dazed and confused. There are picture of scars, staples and swellings within, if that isn’t your bag.

Meningioma is described as ‘the sugeon’s friend’ (by surgeons, it must be said) as it is almost always benign, relatively easy to operate on, and can make big difference to someone’s life when removed.

But as a sufferer, the surgeon’s viewpoint doesn’t change the fact that you are looking down the barrel at brain surgery. Brain surgery is no picnic.

The operation itself

Of course no two operations are the same. Your tumour isn’t my tumour isn’t her tumour and isn’t his tumour. If you are lucky, as I was, the op can take under a couple of hours to perform. More complex rumours in harder to reach places can take much longer. Your surgeon *will* talk it through with you. Listen to them to understand what they will be doing. In practical terms, your own understanding will make no difference, but I suspect going into these things with eyes wide open is the best kind of preparation for the aftermath.

I’m neither therapist nor surgeon but prepare yourself as best you can by concentrating on the end goal. The surgery might be painful and you might be set up for weeks or months of turbulence afterwards but in the long term, you’re setting something very serious right.

Waking up

When you come round, you will probably be in a recovery room rather than your own ward. This room is where the anaesthetists can monitor you as you wake, checking your vital systems and so on. You might even find the surgeon present to try and engage you in conversation for a first impression ‘heads up’ as to your mental functions.

Unfortunately for me, I actually woke up as I was wheeled into the scanning room for an emergency CT scan. Immediately after the operation I suffered a further seizure, likely a side-effect of the operation. This isn’t uncommon, as the operation takes place on the surface of the brain – the stimulation of which is liable to cause seizures.

Pain

Let there be no doubt. Someone cutting your head open causes disfigurement and pain. It may be minor op in the grand scheme of things to a surgeon, but that means next to nothing to you. At the end of the day, this is invasive surgery into your head. Your skull has been cut open, you scalp peeled back and various implements brought to bear directly on your brain. That hurts. No two ways about it.

Not only that, but your head will have been held in place during the operation with a frame to hold everything in position should you start to have a seizure during the actual surgery itself (a thrashing head being that much harder to operate on). This is fastened to your head via pins which are inserted under your scalp. These leave unattractive small puncture wounds around your head, which may weep blood and other fluids.

With all this going on, pain is no surprise. The nature of the pain probably varies from person to person and nature of both the surgery and the tumour itself. In my instance, the pain has primarily manifested itself as a near-constant feeling of pressure in my skull, feeling much sharper during the night as I lay on my side – an act which presumably actually increases the pressue.

Sleep & Confusion

You will be tired. Operations of any kind sap you of energy, despite asking no more of you than to lie on a table. The lingering effects of the anaesthetic coupled to the physical side effects of the operation mean that when you first begin to wake  up you will do so haltingly and probably in some confusion. Falling back asleep is almost inevitable. Welcome it, for the next couple of days you will find sleep hard to come by.

After your first proper spell of consciousness, you will inevitably begin to fall asleep – as even a minor conversation is tiring in those first few hours. You may find yourself slightly confused and disorientated.

During this initial spell of waking, you will be asked questions by the nurses as they take your blood pressure and heart rate every couple of hours. These are standard questions along the lines of “what year is it?” “what month is it?” “where are you?” and “why are you leering at my uniform?”.

In the days following, you might find that you are unable to return to sleep upon waking in the night. My experience has been exactly that: as well as the pain itself, I have found myself massively overstimulated in the night, with my brain apparently set on hyperdrive. I’ve found myself writing emails, sending texts and reading books with feverish hands despite being wrapped in a fug of pain and drugs.

This naturally effects the day/night/sleep/wake balance. At the time of writing, I haven’t got anywhere near a natural bodyclock rhythm going on.

Pain Relief

The pain relief available for such a major piece of surgery seems, to me at least, to be fairly minimal. Paracetamol is, incredibly, the first line of defense. Suitable perhaps for a hangover, I’ve decided it does near to bugger all in the case of head surgery wounds. Better is Codeine. Codeine is an opiate, however, and comes with its own set of problems. While it may alleviate the pain, I suspect it also has a part to play in the agitation and confusion that has been descending during the night.

Other people I know that have been on Codeine have reported “visions” and as I found myself trying to summon Legolas the Elf for help in the night, I can only suspect there’s some truth in that.

Swelling and other side effects

On the second morning after my operation, I was more than a little alarmed to discover that I couldn’t see out of my right eye. My face – fine when I went to sleep – was hugely swollen to the extent that opening my eye was impossible. The picture herein was taken after a couple of doses of drugs, but you still get the idea.

My first instinct was panic: possibly everything in those first few days results in panic. Is this a symptom of something else? A further complication? In fact, it is a perfectly normal part of the post-surgery period.

Pills are given to help alleviate the swelling, and you might be surprised at how efficacious they are at returning your face to some kind of less child-frightening normality.

Scarring

The old rubrick is that chicks dig scars. That’s as maybe, and is fine in the abstract, but you are looking at proper scars. Even with my distantly receded hairline, the surgeon did his best to protect my looks (my face clearly being my fortune) but as you can see, it wasn’t a total success.

Speaking to other patients on the ward, it was clear that even when the scarring was kept under the hairline, it was still definitely visible.

For me, not particularly giving a shit about my appearance and clinging onto the faint notion that actually a dramatic scar would add to my visual allure, this is no biggie. But, if your looks are genuinely important to you then do some mental adjustments. Your world is changing.

You will have staples and stitching, blood and discolouration to deal with. People find it disconcerting. Moving among normal people with a head like this is enlightening. While causing tears in one playground mum, I’m also pretty sure I got extra topping on my ASDA pizza, which probably reflects the cosmic balance.

Support

First line of practical defence are the nurses. They are actually present all the time and have seen everything before. Call on them for pain relief, help with the toilet, whatever.

Second line of defense: friends and family. Visiting times might be rationed, but mobile phones seem to be accepted in hospital in this modern internet age. Be in touch. Let people know how you’re feeling. But also remember that they too might be suffering. Practically speaking, spouses have an equal – perhaps greater – load to carry. They have to watch you going through the shit and be effectively powerless to help. Most likely, they are also juggling normal life: kids, shopping and other rigmaroles that normally are a shared burden. So take time to reassure them, even if you don’t feel like it.

Third line of defence – and not to be underestimated is YOU. Chin up. Face the world. Shit happens. Accept it. Reliance on others is one thing, but ultimately you’re the one who’ll have to face life with visible scars, painful memories and the new realities of life. Don’t underestimate yourself though. The saddest sight of my time in hospital was seeing the guy in the bed opposite, practically collapsing before his operation was even booked. “Paul… what about the depression?” he asked, within mere hours of me arriving back on the ward.

Don’t allow yourself to start from that position. I can’t conceive how you’d recover. People come back from a lot worse and you are no less a person than they.

Occupational Health

It’s early days, but the memory of the thin, disapproving smile as the occupational health advisor looked at the table of sweets and biscuits next to my hospital bed immediately set my teeth on edge. Two days out of brain surgery and the lack of sunflower seeds and healthy raw vegetables on display was clearly antagonistic to this person.

I’m probably being over harsh here, but having just come through an extremely harrowing moment of my life, to find myself the subject of a prim little lecture about getting enough exercise was enough to excite thoughts of violence. “Perhaps we should say,” she began “one packet of sweets then one walk?”

Listen up, buttercup: I got bigger shit to fry here than my BMI. I’m walking out of here and plan on outliving you by several decades.

They do make you run through some tertiary testing of your mental faculties, which is worth paying attention to. I struggled to name objects beginning with ‘p’ which tells me that despite my bravado there are still misfiring synapses somewhere. They also take dimly to smart-arsery. My answers to “name as many animals as you can” (axolotl, ocelot, babirusa, tapir, pangolin, hyrax etc) were received with a chill – evidence in her eyes that I wasn’t taking the test seriously enough rather than (as I thought) evidence of a sparkling intellect and functioning memory.

Anyway, my patience for this first post-op update is at an end. I’ve been up since 1am more or less and feel a little like a Play-doh moptop hairshop figure. Sleep beckons. Take care.

Posted in meningioma | 8 Comments

In which I discover I have a brain tumor

Following my brush with mentalism, it’s rapidly turned into a running joke about the house – which is just the way I like it. Everything works just as it ever did. I’m still forgetful, bumbling but generally healthy and aside from enduring the horrors of public transport it’s been nothing much more than a wrinkle in the fabric of life.

But today was the day of my follow-up CT scan. Having blithely assumed that a non-recurrence of symptoms indicated that I would be in the 60-70% of seizure sufferers for whom the seizure was a never-explained, one time only event, I fair sauntered into the hospital.

The attractive young doctor who put me through the scanner shared a laugh with me as we discussed my case. A CT scan involves lying perfectly still on a narrow, unyielding bit of plastic while they put the bit of you that needs checking through a giant doughnut of plastic and metal.

No sweat. Fifteen minutes of numb bum later, I was released from the bed. But instantly I sensed a change in a atmosphere. Suddenly I was “Mr Carpenter,” as she told me to take a seat in the waiting room while she just spoke to someone.

2 minutes later, I found myself being taken up a corridor and through a door marked “Acute Assessment Unit.”

My stomach flipped.

No-one had yet explained anything to me as I was shuffled from waiting room to waiting room. My blood was taken. A cannula fitted. Little electrodes were attached to my skin by bustily blunt and Northern nurses. I saw my name cropping up on little files and computer screens. One of the nurses stuck a sticker on her chest with my name on it. Internally, I wondered what in the name of all hell would lead me to have my own bloody nurse. I caught wind of the fact that I had been admitted and a bed found for me.

Finally, I found myself sitting in a bare room with 2 disconsolate looking people, staring at my feet and for the first time giving serious consideration to things. Now I’ve watched more than my fair share of episodes of House. I know that a mystery diagnosis quickly leads to some exotic disaster which involves removing the brain via an untested and highly dangerous experimental surgery.

My mind ticks over the possibilities. The word I’m most afraid of is tumour. No-one gets tumours in real life though. That’s the stuff of Hollyoaks cliffhangers, surely? The minutes tick by and I start to pen a book in my head of sage advice I can leave for the kids when I’m dead and they’re old enough to read. I’ve ticked off school (“don’t pay it too much attention”) food (“eat well and eat plenty”) and sex (“boys lie to girls to get it. Girls lie to boys about how much they like it”) when a doctor finally comes to see me.

She’s not a neurologist. But she’s spoken to the neurologist and he’s asked her to tell me the news so I’m not sat here worrying for for any longer. Her first words:

“You’ve got a brain tumour…”

Oh. That’s kind of numbing. As it percolates into the dimmer recesses of my consciousness, I pick up the words “benign” and “early”. This may not be the horror show I have built up in my head.

Eventually having seen a neurologist and consulted Google, it transpires that I have meningioma. It’s a type of tumour that grows in the membrane around the brain and can grow for many years until it’s detected – often by accident when a CT scan is performed for an unrelated matter. The tumour grows in close proximity to the brain and thus can apply pressure leading to seizures (me) and ultimately severe cranial pressure (some other poor sod) which can lead to things such as personality disorders.

The critical thing is that only rarely are meningiomas malignant. There are various treatment courses open, but the most common is an honest-to-goodness brain op, whereupon your scalp is shaved and peeled back, your skull cut open and your brain fiddled with.

So that’s probably what I’m looking forward to. Most people I’ve spoken to don’t believe this, but I’m actually not worried. I don’t see the point – it’s just a fact with potential consequences. But that could apply to a whole load of things in life in general and who’s got the mental energy to worry about things?

Still, I am in the dramatic position to able to say – for a matter of weeks or months at least – “I have a brain tumour.” And not everyone can do that!

Posted in life, meningioma | 10 Comments

Bukkake Espanol…

…is the alleged name of one of my recent  commentors

It goes to show that even in 2011 there is still, apparently, some margin to be made in terrible blog spam of this kind.And presumably money to made in spanish bukkake porn

Who knew?

Posted in Humour | Comments Off

Having a seizure

Friday night. It’s bedtime. Tracy’s already gone up but, despite being tired, I fancy farting around on the internets a while longer. A bit of Facebook… tinkering with the band website… and then noticing that somehow the clock has skipped ahead to near midnight. Turning everything off, I clamber blissfully into bed for a good night’s kip ahead of the camping trip we’ve got planned for the next few days.

When I wake up, I’m immediately confused. My dad’s in the bedroom. As are two guys wearing a green uniform of some kind. I’m sat, naked, on the end of the bed and as I try to stand up in my confusion, I vomit copiously into my hands.

I’m being spoken to, almost patronisingly.

“Come on now.. that’s it… just sit yourself back down. It’s OK.”

What’s going on? I look around and see that Tracy is still here, but that doesn’t account for these people. I feel dizzy and disorientated and my arms and legs feel locked solid. I can’t stand.

The sequence of events is confused in my head now, but somehow I shuffled down the stairs on my bum and was, apparently, sick all over the back of the ambulance.

In the hospital I am wheeled through the corridors on a bed, straight through A&E and into a ward. Lights are shone in my eyes. They fear…. meningitis? There’s a rash on my shoulder that looks to me like burst blood vessels. They can’t take chances though, and several doctors come to look at me to confirm that this isn’t meningitis at all. Still, they take a chest X-Ray.

My confusion is lifting. I feel quite normal, but I’ve no idea what’s happened. Tracy tells me.

She woke up to find me shaking and trembling in the bed. At first she thought she’d caught me doing something untoward, but when I didn’t respond to my name or a poke in the ribs she began to worry. The shakes got more violent and as she turned on the light to come round and look at me, I fell out of the bed, face down on the floor. My knees were pulled up… my fists, clenched. I grunted frighteningly as I shook on the floor and my eyes rolled over in their sockets.

And so now here I was. In a hospital room with a steady parade of people coming in to undress me… get me into a gown… give me water… ask me questions. It’s all a bit stunning and it isn’t until the morning is growing light that I start to piece things together.

Around 60% of people who experience a seizure in the night never suffer a recurrence. For them it is literally “one of those things”. For the remaining 40%, the seizures become a regular part of life – striking randomly at any point.

If the seizures always occur during sleep – as mine did – then life can be lived fairly normally. If not, you can be banned from driving, with all the implications that has for one’s life.

As this is my first seizure – and remember, likely my last – I am banned from driving for 6 months. Not being long in my new job, some way out of Harrogate and 34 miles from my own front door, this immediately panics me. It’ll be sorted though. They’re still ruling out meningitis. To this end, they do a lumbar puncture – sticking a needle into my spine – and putting me on an antibiotic drip.

On day 2 of my stay in the hospital, the consultant comes to tell me my CT scan is clear. That’s funny, I observe, I haven’t had a CT scan. Oh yes you have. Oh no I haven’t. He’ll check.

I was right. They’ve just buggered up the records. They’ve not done the scan, nor booked it in. A whole day wasted, sitting in this bloody room, with no internet, TV or phone – just the old guy in the ward opposite endlessly calling out for “Jean” to take him home.

The hospital is a place of fascination. Sceptical of the state’s efficiency, I note that there are many empty wards in the wing where I am kept. There are also many, many staff. I am brought 3 meals a day and have tea and biscuits in between. Hardly ever do I see the same person twice. I am seen by two consultants who evidently didn’t speak to each other, and a trio of doctors at various points who arrive without introducing themselves. They are good, friendly, knowledgeable people who don’t communicate with each other, and I am in a private room with en suite bathroom while the distressed gentleman who calls for ‘Jean’ is on a mixed ward opposite.

I’m also banned, as mentioned, from driving for 6 months. 6 months! At any point, I could find myself in the 40% of seizure sufferers for whom a single incident turns into a recurring feature of life. Thus I am banned from the public roads.

They failed to CT scan me, but I now wait for an MRI as an outpatient. It sounds quite exciting and I’m just hoping they don’t find anything in there. Apart from a normal brain.

All of which means that I have missed the last family holiday of the year. Still, given what’s happened, it’s a small matter.

Posted in family, meningioma | 4 Comments

Shed no Tears for Murdoch. But…

Rupert Murdoch has sat like a spider at the centre of the web of British life for decades, despite being Australian by birth and American by residence and being largely antipathetic towards our institutions and culture. Much of what you probably hate about modern Britain – the vacuity of celebrity, the remorseless avarice of some areas of enterprise, the shrivelling of public debate – takes as its blueprint the success of the Murdoch media.

Such has been the spectre he has cast that Murdoch cast-offs like Andy Coulson have been sought for their insight like living witch bottles to keep the media from tearing down the doors of power. And to counter these Murdochian djins, malevolent spectres like Mandelson and Campbell have been bred to fight poison with poison.

And we have all supped at the cup. The leering barrow-boy charm of his Sunday offering has sustained many a happy, hungover conversation. Like Mr Punch, The NOTW has been a touchstone of carnival grotesquerie for anyone who wishes to see pomposity pricked.

Eventually, it was all going to go to far. Because much of Murdoch’s populist touch was a pretence. A republican who wrung every penny out of Royals – triumph and tragedy alike. A champion of hang ‘em and flog ‘em whose empire happily broke confidences and the law in search of a story. A conservative who gave his blessing to 13 years of socialism because he saw the way the wind was blowing. An expounder of competition except where it affected his own interests.

Without a central guiding principle, these internal contradictions could only ever corrupt. The larkish high jinks of rummaging through some minor celebrity’s bins eliding slowly but surely into the hacking of a murdered girl’s phone. Along the way there have been journalistic highs to match the lows, but at some point a line has to be drawn.

But also: don’t be mistaken: the barely-concealed glee of The Guardian and the BBC is nothing to do with the triumph of morality (as Autonomous Mind reminds us). Murdoch’s popular touch has been a near constant affront to the soft left. What they routinely call “right wing demagoguery” or “pandering to the lowest common denominator” is just a reflection of the frustration they feel that outside the establishment their message isn’t heard.

Because aside from Murdoch, there are no alternative voices to be heard in the media. The BBC, Independent, Mirror and Guardian, every quangocrat, civil servant, pressure group and corporate press release is dressed in the rituals and language of the left.

The myriad agendas of ‘fairness’ and ‘equality’, the chimaerae of ‘phobias’ and ‘isms’ and ‘sustainability’ only find their popular rebuke in The Sun and the News of the World. Only here could the pompous vacuity of the EU be subject to the full depth of popular ire in words of under 2 syllables. And now even that is to be diminished.

While a Murdoch curtailed is a blessed relief, a world without Murdoch at all is no triumph for anything. If all we are left with are lone voices, competing for air in the blogosphere, then we have all lost.

Posted in Politics | 2 Comments

The Kings Head, Bradford: Superset Live!

For some reason that remains unexplored, the centre of gravity for the band’s recent activity is definitely moving towards Bradford. Maybe Bradfordians, for all their faults (mainly that they aren’t from Leeds) have better taste in music. Who knows?

Anyway, this followed a pattern set by quite a few gigs recently: while the Kings Head builds itself around music we still had to work hard to win over the punters. The first half of the set was played to around 15 more or less disinterested punters who mustered nothing more than polite applause here and there.

One guy – occupying the fashion space at a point exactly between Captain Jack Sparrow and The Terminator – was making his feelings quite plain by sitting with his back to us for pretty much the whole set, tapping his foot only occasionally. But hey – that’s fine: not everyone likes everything and if coming back from the future to drink rum and idly finger doubloons is your bag, then more power to you!

Years and years of gigs like this has taught us one thing: if the audience aren’t enjoying it, make sure that you are. Pull some shapes…. crack some gags… rock like donkeys and never – NEVER – become self-conscious.

But then, in the mid set interval, the place suddenly filled up with a slew of interesting people: some of whom we’ve actually met before at other gigs. There was dancing! Laughs! Applause!

By the end of the set, everything was warm and lovely and the room was full of love and we’re back there on the 20th of August. If you were there, thanks as ever and we hope to see you again.

Setlist

  1. Paperback Writer – The Beatles
  2. A Town Called Malice – The Jam
  3. North Country Boy – The Charlatans
  4. Beetlebum – Blur
  5. Queen Bitch – David Bowie
  6. Black Dog – Led Zeppelin
  7. Tin Soldier – The Small Faces
  8. Can’t Explain – The Who
  9. Be Bop-a-Lula – Gene Vincent
  10. I Got You (I Feel Good) – James Brown
  11. Green Onions – Booker T. and the MGs
  12. Substitute – The Who
  13. Come Together – The Beatles
  14. Sympathy for the Devil – The Rolling Stones
  15. Last Nite – The Strokes
  16. All or Nothing – The Small Faces
  17. Where Have all the Good Times Gone? – The Kinks
  18. Fun, Fun, Fun – The Beach Boys
  19. Seven Nation Army – The White Stripes
  20. Step On – The Happy Mondays
  21. Subterranean Homesick Blues – Bob Dylan
  22. Steady as She Goes – The Raconteurs
  23. Everything I Want – Superset
  24. In The End – Superset
  25. I Still Don’t Understand – Superset
Posted in Gigs, Music | 3 Comments