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Biopsy day

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Tomorrow - Friday - is biopsy day.

I am due at the hospital at 7am. The intention is that I'll have a one-night stay and be allowed home on Saturday.  Discharge is usually 'by lunchtime' (ha, presumably so they don't have to feed you!)

That does mean there won't be a blog update immediately - the hospital website assures me that wifi and phone coverage are both highly limited (and, of course, once I'm on the ward after surgery I'm pretty sure that'll be a no-mobile-phone zone).

And I thought I'd let you all know that, so nobody is surprised by it going quiet smile

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Sarah sitting on the steps outside the Fitzwilliam Museum in Cambridge

Pre-admission stuff

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An unbelievably sleepless night followed by an incredibly anxious morning. I surprised myself by managing to have breakfast.

Due to a road closure, we unexpectedly ended up with just me and Lawrence going, so we are quite proud of ourselves for being grown ups today. We navigated the 9am Cambridge traffic to find the hospital, the car park and the ward all in good time.

Nurse did all the expected stuff - height, weight, medical history, MRSA swabs, huge pile of blood tests. She took my blood pressure which was an astonishing 125 / 76 - that's bonkers! How can my blood pressure possibly be normal at a time like this?!

CT scan done with contrast - twice, because the first time they didn't get my nose in right! The CT is a bit of magic because it will be used as guidance during the biopsy, i.e. they'll know where they are even though they can't directly see.

Utterly exhausted by the time we got home. Did the sensible thing and had an afternoon nap, which was lovely. On waking up, I've already started getting anxious for the next bit. I think a GP chat will be in order tomorrow, because I can't comprehend how I'm going to cope with the up to three weeks for biopsy results...

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At last - something to focus on!

Pre-admissions stuff - bloods, CT, possibly ECG, etc - is actually happening.  Tomorrow, Wednesday 13th May, at 9.40am at Addenbrookes.

Feeling relaxed for the first time in days big grin

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Sarah sitting on the steps outside the Fitzwilliam Museum in Cambridge

Waiting

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Apparently I should expect to hear from Addenbrooke’s today on when they want to see me for what this week (bloods/CT due before biopsy, which is supposed to be Friday).  If I haven’t heard by tomorrow morning, then the consultant’s secretary will chase up for me.

It’ll be nice to have a plan for this week.  It turns out that I’m not very good at waiting.  It’s all well and good the consultant being so relaxed about it all – but he does do this all the time.  This is my first brain tumour, and the waiting, waiting, waiting is no good at all.  After the biopsy it’ll be anywhere between 1 and 3 weeks before I get results.  That’s going to be really, really hard.

I’ve realised I’m napping a lot, not due to tiredness, but because sleep is some respite.  No matter what I’m doing, it’s not generally enough to distract me from You Know What at the back of my mind.  Doesn't matter if I'm thinking best-case or worst-case (and it veers rapidly between the two), it's still there and pestering me.

Cold-callers are getting a bit of a sharp response today (usually I don't answer the phone to 'unavailable' or 'witheld' but I can't do that at the moment...)

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A couple of things I've just thought of, me being me I have to correct/update myself big grin

The cavernous sinus is not inherently inoperable.  It is in my case due to it being full of tumour which is all wrapped around the important bits.  It's possible for people to get tumours here that sneak in between stuff and can be removed.  So, if you're googling on my behalf and see people who have had ops - well, that's great for them, but not a help for me.  The surgeon I saw has done over 400 skull base tumour removals - so I think if he says it can't be done, we can be pretty damn sure it can't be done.

On the calcifcation and the CT.  Calcified = benign.  However, not-calcified does not = not-benign.  Not-calcified = no idea so let's biopsy.  Having to have the biopsy still doesn't mean we're dealing with bad news.

Finally, my dad the very clever man thought to ask how long the biopsy results take.  Apparently it is 7-10 days at least - that's if it is fairly plain tissue.  If it's more calcified, then they have to dissolve out the calcium first, so biopsy results can take 2-3 weeks.

What that means is all in all I'm living with uncertainty for quite a bit longer.  This is taking a bit of getting used to.  Obviously it was all scary and unknown when I was told, but the expectation was that yesterday I'd get context and information and we'd know what's going on.  Today I'm getting back used to the idea that knowing anything will be quite a while yet...

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Neurosurgeon visit

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Edited by Sarah Cornell, Thursday, 7 May 2015, 17:00

One word to sum up the neurosurgeon appointment: inconclusive.

That's not a brilliant word to come home with, but it could be a lot worse.

It turns out that the tumour is in the cavernous sinus.  This is a little space in your skull that's behind the eye and nose, and in front of/below the brain.  It's a space full of Very Important Things - among other things, the inner carotid artery (which takes blood to the brain), the optic nerve, the oculomotor nerve and the olfactory nerve.  As such, this is an area in which it is impossible to operate, because it would be certain to do more harm than good.

However, the tumour has done a bit of bone remodelling as it has grown, and extended itself in to the nasal sinus.  This means that it is possible to go up there and grab a bit of it, so we can work out what it is, from which next steps are decided.

Next week they want me to have a CT scan, some blood tests (for the anaethetist to reference), and a biopsy (under general anaesthetic/one night hospital stay).

An MRI is good for looking at tissue, but not at bone.  CT is great for looking at bone.  The CT scan will tell us how calcified the tumour is.

If it's very calcified, that makes it in effect a sealed unit.  I've simply got a pebble in my head.  That will by definition be benign - it can't grow any more.  If it's totally calcified, there's not even any point taking a biopsy!  This would then be a case of an annual scan to make sure it stays that way.  Any symptoms - with my vision, with my headaches - just need to be managed (and as the neurosurgeon pointed out - there's actually nothing to say for definite that the recent monster headaches are even related to this; my migraine might just have gone intense because migraines often change with age, and the tumour is something we would otherwise never have known about).

If it's not completely calcified, then there will be a biopsy taken of the bit that's grown across in to my nose.  From this, it will be determined if the tumour is benign or not.

If it's benign, then we follow the same procedure as if it's completely calcified - check up on it every year.  If at any point it starts showing signs of waking up, we zap it with some radiation to shrink it back down again.

If it's not benign, then it'll be chemo and radio and all that sort of stuff.  This is a vague sentence because while I acknowledge the possibility, I'm not going to give up any of the apparently limited space in my head to think about it until there is no feasible alternative!

The neurosurgeon himself can only be described as extremely relaxed about this.  I'm only getting my biopsy next week because he happened to find an ENT surgeon available to do it next Friday; but he said under normal circumstances it might take a month to get a date that can be done (yes, even privately), and if that were the case, no problem, this can wait a month.  Indeed, we could re-scheduled next Friday if that weren't convenient, if we were going on holiday or something (we were going on holiday in late May; we've cancelled it all, possibly unecessarily as it now turns out, but I'll probably be happier being close to Addenbrookes until we know for definite what is going on).

So, inconclusive, but when that's presented to you by an undeniable expert who is completely relaxed about it, that's actually somewhat reassuring.  While I'm not exactly comfortable with the technically accurate words 'inoperable brain tumour' yet, I am after only a couple of hours beginning to see that they are not necessarily a Very Bad Thing.

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I have cried so much in the last few days, and very few of those tears were for the reason you might expect.

If you'd asked on Saturday morning, I would have defined 'overwhelmed' as 'what it feels like when you're told you have a brain tumour'.

But it is as nothing to how I feel about the absolute outpouring of love, support, kindness and caring that has come from everybody in the last few days.

My email, my Facebook messages, my work email, my PM box at the music forum, my text messages, just everything, everywhere is full you lovely people being lovely.  People I talk to most days of the working week, people I bump in to at the office about once a quarter, people I live ten minutes walk from but might only manage to see once a year, people who are on the other side of the planet, people I only know by online pseudonym, people I haven't seen since we left university or school, every single damn one of you.

I suppose it is one of those things that generally goes without saying - I would hope that you, as my friends, would know that if you needed something from me, you would ask, and I would be there.  And suddenly I'm on the receiving end of an awful lot of people who feel the same way about me, and are saying it out loud.  It is amazing, overwhelming, moving ... completely indescribable, really.

I did warn many people that I might be slow in replying, and I said that because I thought there might be a few people to get back to.  There are in fact so many that you may well just have to make do with this generic thanks from me for now.

I know a number of you have been in touch with Lawrence to offer him your support as well, and I am deeply appreciative of that.  It is understandable that the focus is on me right now, but there are many more of us involved in this - so do me a favour: look after one another just as much as you are all looking after me, my dear, dear friends.

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Neurosurgeon appointment now confirmed as Thursday afternoon.

Enormous list of questions being built wink

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How we got here...

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Edited by Sarah Cornell, Tuesday, 5 May 2015, 09:50

This'll be a very long one, but it will let you know the story so far.

I should start at the beginning.  But it's difficult to know where the beginning is.  It may well have been when I got my first migraine, aged 19 or 20.  It could even be well before that.

So we'll start with a more recent beginning.

Very end of January 2015.  A migraine that was not particularly more painful than those that had come before, but kept on, and on, and on.  A few days after it started, my right eye began to ache a lot, especially when I looked left.  The headache started bilaterally - I've never really had the one-sidedness that's common with migraines - but it migrated to be on the right side and around the eye.  I visited the GP on day 7 - it was the first time a migraine had gone to a week (and usually even if they went on 5 or 6 days, they were clearly fading out by then), and the eye stuff was just weird.  The quite reasonable conclusion at this stage, after a look in the eyes and a few simple checks, was that I had had a migraine that was just unlike those I'd had before.  The headache went away after 10 days, though the eye pain lasted a few more days, but then it was all over.

Late February 2015.  Routine eye test.  I told my optician about the above, and he thought it might be vision related.  He determined that I needed reading glasses in addition to my normal glasses - I am, perhaps, very slightly young to get such things, but only very slightly.  You may well know that my eyes - particular the right - have always been dodgy, so getting my old-age reading glasses early was no great surprise.

7th April 2015.  Travelling home from work (on the tube) I was aware my head was aching a bit.  I sensibly took some painkillers, but it was when I stood up that I realised this was another Big Headache.  A couple of days off work, topping up on the painkillers - much like a normal migraine, until the eye pain started again.

Off to the GP, who thought this was odd to have a second strange migraine; by this time I'd also noticed - and remembered to mention - that my pupils were different sizes.  That doesn't have to be a sign of anything - apparently about 20% of people who have different size pupils have always had that, they've just never noticed!  Standard blood tests ordered as a starting point, though, on the assumption that something was causing this, we just needed to work out what.

Before coming home after the appointment, I thought I'd drop in on my optician - who was more than happy to take another look at my eyes.  My right eye was definitely misbehaving - covered my left eye, asked me to read the chart, and I could manage the top three rows.  10 seconds later, I could read the entire chart, like normal (with glasses, obviously; without glasses, I'd never even get the first letter!)  My right eye was able to focus, just in it's own time.

I remembered again to mention the pupils being different sizes.  That's when things changed.  Several tests later, an ophthalmologist was recommended - from the list of those available at the local hospital, three were specifically recommended (my employer gives me private health cover, for which right now I am extremely grateful!)  I phoned the hospital, made the appointment, and rang back the optician's office to say they could address the referral letter to Mr X, who I was seeing on the 27th.

I think it took less than 20 minutes for my optician to ring me back.  No, he said, you do not wait until the 27th.  You phone the hospital, you find which ophthalmologist has the next available appointment, any of them, and you get there by whatever means (I'd gone for the first available late-ish afternoon appontment, so Lawrence could drive me there and back).

20th April, 11am, and I'm getting on the bus that goes from the end of my road to five minutes walk from the hospital.  12.30, and I'm in with the ophthalmologist.  It starts routinely, but after a while I could tell something had changed.  He was interested. Now, it's not like you want your doctor to be interested in you - that means it's not something boring and routine - but it does mean they aren't going to let go until they've worked something out.

There were two blood tests ordered - one to rule out thyroid eye disease, one to rule out myasthenia gravis, both of which didn't quite fit but seemed far more likely than his favoured diagnosis of the extremely rare ophthalmoplegic migraine.  This is ludicrously uncommon - 0.7 per million people per year! - but it seemed to fit everything.  Of course, just to be on the safe side, we'll do an MRI of brain and orbits as well.

At the MRI, I was told to expect the results to get to my consultant in about four days.  Except it only two and a bit days until he phoned me, at 7.40pm on Friday night.  He'd got the report from my scan, although not the images, and he was very sorry to tell me that there was a tumour in the skull base.  His next task was to phone the on-call neurosurgeon at Addenbrookes to find out what happens next - he's an ophthalmologist, this is beyond his area of expertise!

I put the phone down.  Some swearing ensued.  Dinner - which the oven timer announced had just finished cooking as the phone rang - ended up in the bin.

An hour later, he got back to me - he'd spent about half of that time hitting re-dial to get through to the person he needed to speak to!  The procedure is that the case is reviewed by a multi-disciplinary team (MDT) who look at the case, work out what the problem is most likely to be, and then pick the best specialism/specialist.  The team includes people like neurologists, neurosurgeons, oncologists, neuroradiologists, radiologists, and various other extremely clever types.

The ophthalmologist phoned me back on Saturday morning to tell me that the team had met and reviewed, and recommended a specific neurosurgeon.  Who is currently on holiday, but is back on Thursday, and if I phone his secretary to make an appointment, I should be able to see him then.

Not that any of this is good, but it's somewhat reassuring that they haven't assessed me as 'get in to this hospital right now this second'.

Of course it's a bank holiday Monday as I write this, so I haven't actually been able to speak to the secretary yet.  I've left a message and if she's not phoned me first thing tomorrow morning, I'll be phoning her.  She should have all my details/reports/scans/etc emailed over already.

So there's not a lot for me to do.  It's a case of trying to keep calm and carry on.  With any luck, I'll have an update for you on Thursday of what we can expect to happen next...

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Sarah sitting on the steps outside the Fitzwilliam Museum in Cambridge

Welcome

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Edited by Sarah Cornell, Tuesday, 5 May 2015, 09:48

I can only think of two reasons that you are here and reading this.

Firstly, I've given you the link, in which case, hello, welcome, it's lovely to see you.

Secondly, you've stumbled upon this while browsing the OU blog pages.  In which case, hello to you too, you are welcome to join us for the ride.  Though it is only fair that you know what that ride is.  On Friday 1st May 2015 I was diagnosed as having a brain tumour.  This blog is intended to be my easy way to update friends and family without having to send lots of emails or remember who is on which social media and stuff like that.

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