Monthly Archives: February 2016

What Gives?

escape2016 has been a cruel year.

A seriously ill relative.

Three health scares, one after the other, including debilitating flu.

Too much unexpected time off work, so less money coming in.

And MS is playing up.

All in all, when I raised my solitary glass of champagne as the last dregs of 2015 drained away, I could never have foreseen just how much my world would change only a few short weeks later.

Back in 2012, when I was first diagnosed with MS, I had one aim – to ensure The Teenager had as happy a life as possible, despite everything. And I’ve succeeded (ish), until now.

I’m rushing around, working, studying, catching up with Ill Relative Business. I’ve cancelled book club, haven’t been out with friends for three months and I can’t remember the last time I did something just for fun.

I’m months behind in my Uni work – my Next Great Novel is on hold. I pray I can carve out some time to catch up. I’m floundering.

So, what gives? What can I let go of?

I look a mess. My hair is straggly and un-cut. I veer from over-eating to existing on adrenalin and Lucozade. My plans to create a Scandinavian-style capsule wardrobe have been shelved. There’s mould in the bathroom and I just can’t be bothered to sort it out.

We all have to cope with unexpected scenarios and juggle a stupid amount of balls in the air. Behind it all, MS looms large. My foot drop is back with a vengeance and my memory seems to be shot to pieces. I can barely remember what week we’re in – in short, normal life is on hold.

But – I’m trying. Even the simple stuff like keeping on top of the laundry is keeping me sane. If I can meal plan a few days in advance, it’s a result. And if I can get to work and put in a full day (although my nickname’s ‘Half-Shift’), it’s all good.

Yet in the back of my mind, I fear the relapse. I fought back through a horrendous bout of the ‘flu, but a relapse is different. It will pin me down and not let go. And what do I do then?

Despite it all, I am trying to remember to look on the bright side of life. There’s daffodils for sale, the sun is shining and I am still going strong-ish.

I’ll get there. Won’t I?

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I’m So Last Century …

dinosaurSomeone asked me the other day how I get The Teenager up for school.

Easy, I said, just unplug the Wi-fi.

Sit down and wait for the piercing scream of abject agony.

It works – try it.

Anyway, as I’ve been jotting down my Master’s dissertation by hand these last few weeks, The Teenager has been streets ahead of me, organising his A Level files at the stroke of a button.

He laughs at my hand-drawn mind-maps. He chortles when he sees my scribbles, turning his ipad towards me, shining with beautiful study notes.

I take off my fingerless gloves and turn the heating on. I gently explain to him that Great Art involves Great Suffering. I am trying to channel words and images into a superb piece of writing. I could in fact be The Next Great Novelist, given half the chance.

Until I’m rudely interrupted:

‘Muuuuuuuuum. Mum. Mum. What was it like BI?’

‘Wha?’

‘D’uh. Like. Before. Internet?’ Where you deprived? Did you feel, like, sad?’

‘Ah. No. We went to a place called A Library and looked up an Encyclopedia. That’s a book.’

‘Sad,’

‘Not really.’

‘You mean, if you wanted to find something out, you had to, like, order a book? Really?’

‘Well. Yeah.’

‘Oh M’God. ‘

I am a dinosaur. The Teenager cannot comprehend a life without facts at his fingertips. I could be impressed, chuffed even. Until he sends me bizarre links of what is trending on Twitter.

Take yesterday. The Teenager should have been researching British Politics. Instead, I had a breathless text, ‘ya seen Twitter?’

‘Not yet, have you cleaned your bedroom?’

‘So funny, have you seen, OMG, hysterical.’

‘What?’

DamnDaniel.’

‘Oh really? A kid?’

‘S’fun, s’like real.’

I worry.

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MS – The Interview

forgiveMS is fairly busy these days – 100,00 of us to pester in the UK alone and millions across the world.

So it was fortuitous that it could take time out from a hectic schedule to settle down for a cosy chat:

MS: How’s things? Bad, I hope? Any more nerve pain?

Me: Funny you should say that, but yes. Don’t you ever give up?

MS: Short answer: No.

Me: Long answer?

MS: Well (long pause). It’s interesting, don’t you think? Push you just that little bit more?

Me: Really?

MS: I’ve always said – and no word of a lie – you have to be tough to live with MS. I have, haven’t I?

Me: Erm, yes?

MS: So. The way I see it, I’m doing you a favour? So, it’s bad, it’s sad, it’s painful, it’s isolating. And?

Me: What do you expect me to say? Thank you?

MS: Actually, yes. Whoah, stay seated and put that vase down. Listen. If I’m honest, it’s fun – all that freaky tiredness, making you walk funny, seeing you drop stuff. It makes me laugh. And?

Me: And what?

MS: Well. Let me think. You were diagnosed in – hang on – 2012? Yes?

Me: Yup.

MS: And what’s happened since then? Still with that bullying boss? That useless boyfriend? Still harbouring a vague notion of, and I quote, being a writer?

Me: I know what you’re doing.

MS: Good.

Me: You’ve ruined my life. I went through hell. My son was scared. I was scared. My future is uncertain.

MS: I haven’t ruined your life – you have a different job now and you love it. Your son is doing brilliantly. You’re not scared, you’re fearsome. And like anyone else on this planet, your future will always be uncertain. Deal with it.

Me: Why do you pop up so unexpectedly? Cripple me with absolute fatigue when I least expect it?

MS: Like I said, it’s fun.

Me: That’s unfair.

MS: Life is unfair. Are we done now? I’m very busy you know.

Me: I hate you.

MS: I hate you too. So we’re quits.

And with that, MS leaves.

But not quite …

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Ya Flu Sucks …

fluLast Tuesday in work, the boss stared at me in a somewhat odd manner.

‘Oi, Half-Shift, you here or what?’

‘Oh, er. Yes, that colour scheme looks great. White looks fab with, um, everything don’t you think?’

‘Nice, but we’re talking about the roof plans?’

I tuned back in from wherever I was. I felt … wrong.

I left work early with, ‘ta-ra Quarter-Shift’ ringing in my white-noise ears.

At home, I collapsed onto the sofa (a recurring theme) and lay there, dazed (another recurring theme).

Strangely though, I didn’t feel like eating any chocolate. It was probably then that I knew something fairly serious was up.

That night, I crawled into bed and spent hours tossing and turning, covered in sweat and having the strangest dreams. I woke up long enough to cancel two appointments and went back to bed.

When I woke again, I couldn’t get out of bed. I tried. Then tried again. Eventually, I tumbled downstairs and collapsed again on to the sofa. I was feverish and aching.

Hours later, I dressed in yesterday’s clothes and dragged myself off to a chemist. He noted my long list of symptoms and finally told me I was one of the unlucky, ‘Had the flu jab, got the flu’ peeps.

I questioned him closely:

‘And that would explain the aching joints? The insomnia? The nausea? The headaches?’

‘Yes.’

‘And also the feverish dreams?’

‘Yes.’

‘What about the complete lack of appetite? And do you think this might be a lasting symptom (ever hopeful)?’

‘Yes. And, ah, no.’

Right. Panic stations.

I haven’t felt this ill in a long, long time. I can always somehow truck on, but this, this was on a different level. I was reduced to a gibbering wreck. No longer could I hide these symptoms from The Teenager when he found me on the sofa staring at ‘Judge Rinder’ with glassy eyes.

‘Hi! I don’t seem to be able to get up off the sofa. Not MS, just the flu. Nothing to worry about.’

The Teenager patted me on my head.

‘Mum. You know, you’ve always been kinda brave by keeping your MS symptoms away from me. I know that. I’m not like, stupid. But, like, let me help.’

It was hard, but I did. He cleared away glasses and cups, put out the rubbish, tidied up the kitchen and got me juice. He fetched my unread book-club book from upstairs, fed the cat, closed the curtains.

The next two days were a blur of willing myself to get better. Flu seems to exacerbate all manner of MS symptoms, so along with the aching and feeling of being run over, I was coping with more foot drop, bonkers balance and an interesting speech slur.

And now, five days on, I’m getting slowly back to normality. Or something like it.

One thing’s for sure. This has been a terrible year so far – surely I’m due some good news?

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Hope Beyond Illness

ShulamitShulamit Lando is my guest blogger today; she is an inspirational therapist and life coach – have a look at her website. You can also buy Shuli’s book here.

 

One develops great courage from traveling the journey of illness.

At the beginning it is like a strange, formless, indefinite entity that is born at the moment of the diagnosis –an undesired creature indeed.

But it was born and now it is right here with you, as you watch it stubbornly develop, nurtured by every step you take toward your capacity to accept things as they are, your ability to deal with your reality better and, ultimately, to your healing.

Every step of the way, from the simplest fear of tests and treatments to the overwhelming dread of facing and dealing with the endless “what ifs”, makes the creature develop into a specific shape until you can recognize it as what it really is: a POWER that was not there before.

One needs huge amounts of courage in order to face the fears that illness brings to our startled minds—fear of loss, of disability, of suffering, of uncertainty, of what will be and what will never be again, of depending on others, and of so much more. And ultimately, of course, the fear of our own mortality.

“Courage is Grace under Pressure”, Hemingway told us.

When we feel we are about to drown in a life-threatening storm, the human spirit is capable of extraordinary achievements. The human spirit is undefeatable, no matter the adversity. No matter what challenge is presented to it, sooner or later it will take up that challenge with a burst of hope, and find a way out, a way through, a reminder of the courage in you and of the undeniable way that you have already been able to overcome many hurdles in your past.

The human spirit is invincible; it is that part of you that endlessly seeks healing and doesn’t give up, that always needs to find a way out and to keep going until you heal. And you will know that you have arrived at your healing when you experience serenity in the presence of your disease.

I had the choice to continue being who I had been till that moment, with the same skills to face a life of illness, or I could choose to flow with what I was supposed to become. I chose the second path and indeed I became a new self.

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