Before My Time

Flowered Too Early

I gasped, trying to clutch reality, trying to stop the world from completely slipping from my fingers.  I can do this, I tell myself.  I cannot believe otherwise.  If I do then where will it end?  The world, my world, my life, everything will fall away, it will be the crash of a tower of bricks, a slight wobble here and there, the slow bend of the tower  but then the inevitable crash.  It will fall.  And all will be lost.

I tell myself to hold tight, I grip my hands tightly,  cramped-ridden knuckles that rarely seem able to straighten anymore, as if life, health, self, world could be something tangible, something that could be grasped, something that could be kept held of.  I can’t keep hold of them; they’re more slippery than fine sand grains.  And the tighter I grasp, the faster they are squeezed from my grip.  I cannot win.

I gasp, every breath is a struggle.  The physical world around me swims.  The ridged concrete path swirls in a blur of motion.  The metal fence posts alongside do tricks that no fence post should ever be able to master.  The world will not stay put.  It will not allow me to get a handle on it.  I cannot keep it still.  I grasp out at it but it moves, slippery and fast, and unreachable.  Everything is beyond me.

You’re not meant to get motion sickness walking.  But I do.  It’s not like I have mastered some locomotive state.  Or maybe I did once.  Once upon a time, I was able to keep up.  Keep up with what?  Life, self, health, world.  No more.  I am slower than the World’s Slowest Walkers.  I know.  They keep overtaking me.

I struggle to breathe, like an asthmatic at the end of a sprint.  But I have gone nowhere fast.

My body ridicules me.  Me, that self I dream of being.  I cannot be.  I am crippled and handicapped and fighting a body whose war I barely even understand.  I am conspired against daily.  I lose daily.

I no longer feel safe walking by myself.  I don’t have the breath to think let alone scream in defence.  I feel shaky, vulnerable, weak, frail.  I am not myself anymore.  I can’t walk out into the world with the bravado that I used to.  I can’t take the time to enjoy a moment of solitude or the world around me.  I am too busy fighting.  There are days when I walk so slowly past front gardens that I get to know each and every blade of grass by name.  I don’t admire flowers, they get boring when you’ve spent five minutes walking passed the same one.  They taunt me, moving free in a breeze.  They have more speed than me.  They move whilst I am motionless.  One day snails will overtake me.

I muddle words and can’t remember whether I had conversations out loud, in my head or in my sleep.  I can’t remember what needs doing or even what I have done.  I forget where I am halfway through a recipe.  I forget ideas halfway through sentences.  I forget.  I forget.  Me, who has always been a memory keeper.  Me, this is my role, this my usefulness in the world, because I can remember.  And I can’t.  What have I left?  I console myself with sarcastic humour, reminding myself that at least at some point I will forget that I ever even had a memory.  But at the moment?  Oh no, I remember.  I remember the glory days.

The glory days that never were.

A golden age only exists in nostalgia, a better time compared to current woes.

And I do remember that there have never been glory days for me, I have never succeeded, not even at being myself.  And now I feel perhaps I would have a chance but it is all being dashed away from, like that tower of bricks.  I cannot stop them falling, I cannot stop the present and I dread the future.

My hand shakes.  I am weak and vulnerable and pathetic.

This is not me.

This is not who I want to be.

This is not who I should be.

I forget names, faces become foggy.

I mix up all my nouns.  If I can even remember any.

I get my sentences backwards.

More vicar, tea?

I don’t know if the world notices but I do.  I notice.  I see every single mistake, every single failure.  I, who have tried so hard my entire life to hide my weaknesses, my problems, now have them writ embarrassingly large across each and every conversation and each and every day.

This is not me.

The slow, painful steps that I am taking through life and the world.

This is not me.

I sit motionless, lost, unable to find the strength to do anything.

This is not me.

I cannot form sentences.

This not me.

I cannot remember.

This is not me.

But it is.

It is who I have become.

I didn’t get a choice.

I would have liked a choice.

Because I would really like to have life back.

I want another chance.

But something tells me it’s too late.

The sand has tumbled from my hands, I never had much anyway, and it cannot be found again.

I have lost.

Everything.

I have lost me.

Busy Bee

[ there would be a picture here ]

Are bees busy?  Well, what I mean is, why do we perceive bees to be busy?  Most bugs and bichos are notable for their state of activity rather than otherwise.  Take the ant.  Ants are industrious.  But maybe they aren’t cute enough to enter popular colloquial speech?  (Are bees are cute?  Husband would argue otherwise, he has a major problem with the entire species (and anything else that speaks the same language – bzzzz) because he cycled into one once upon a time whereupon the unfortunate creature stung).  Ants creep.  Humans, generally, don’t really trust creeping things.  Or is it simply the pleasing alliteration of the phrase?  Well, in that case, maybe we could make a case for assiduous ants.  After all, being busy doesn’t have to have a purpose.

(I’m going with alliteration, the French apparently don’t do bees).

Anyway, that’s a nice random paragraph, a classic case of my idiosyncratic mind in full operation, but there really needs to be a point to this post.  I mean, you don’t come here just to read random wafflings about apiformes, do you?  No, I didn’t think so.

The point that I’m trying to make, and may well do so eventually, is that I have been a busy bee.  Or just a busy human.  Very busy.  And, of course, being busy has meant that I’ve also had to spend quite a bit of time recovering.  That is why I have been absent.  (Is absence usually associated with busyness?  Hmm).

Life has calmed (hopefully) and I’m bored of being rather poorly and bed-bound so I might have recovered, in which case, blogging will resume.

Shortly.

Hopefully.

Maybe.

It’s Been a Bad, Bad, Bad Day

Where do I start?

This morning?

When I got up at ten to eight so I could be ready by half past nine only to discover that it was now, for reasons that I really can never fathom, actually TEN to NINE?

I don’t do mornings at the best of times.

I am very slow in the mornings.

To find that, for reasons that I can never really fathom, I now only had a mere half an hour to eat breakfast, shower, do my hair, get dressed and get ready was a little bit too much to ask.

And definitely a lot more than I can cope with.

I should have given up then and crawled back into bed.

And yes, feeding me is a priority.  Without food, I cannot do anything.  In fact, I normally wake up at half past eight, have my breakfast then go back to sleep.  Without food, I don’t even have the energy to sleep!

But, somehow, unbelievably, I managed to do it.

I was frazzled.

And had to exit the house unpainted.

I don’t like going out of the house without my slap.

It doesn’t feel safe.

It’s definitely not kind to or fair on other people.

I was frazzled.

And then a half a dozen other minor things just didn’t go well.

You know, the sort of piddling trifles that really aren’t hugely important most of the time but when you’ve already had such a rotten start, they really don’t HELP.

I had to leave early, a proactive choice because I really didn’t have the energy to deal with a panic attack.

And by that point slowly crawling home on foot up a very nasty steep hill was actually preferential to staying put.

I came home.

I knew that I had a cake to make for this afternoon.

A basic, simple, straightforward cake.

(The previous one wasn’t, at all, and I will be telling you all about that another time but that cake does not belong on Bad Days, it was a surprising triumph (relatively)).

I made one exactly the same earlier in the week but plain not chocolate.

It took 45 min in the oven.

I started with just over three hours to go before I had to go out, me and the cake.

The cake, naturally, because this was already a very Bad Day, did not cook.

How can a cake choose not to cook?

I had to leave without my cake.

I was feeling so miserable by this point that I left the house in my slippers.

There was no way that I could face boots and bootlaces only to take them off five minutes later at my friends’ house.

I remembered my knitting bag.

And my mobile.

And the DVDs that I’ve been promising to lend for the last month.

But forgot my ‘handbag‘.

My handbag is also a security thing.  I feel safe with my handbag.

I didn’t feel safe without it.

It was the kind of day where having my handbag with me would make all the difference.

Well, probably not, but I’d at least feel slightly better equipped to face the Bad Day.

(Maybe I should start sleeping with my handbag as some sort of Bad Day prevention device?  Hmm).

(Come to think of it, I didn’t sleep well either).

It wasn’t too bad though.

There was a delectable cream sponge and profit-roles.

I like profit-roles.

Then I got the news that my external hard drive is irredeemably fudged.

I have lost my entire life.

Because, of course, my entire life is stored in data on a 500 gb hard drive.

Well, a lot of it was.

I think the Baby Photos were on it.

And all my downloaded knitting patterns.

And all of this year’s photos.

(Husband made a really cool shark biscuit the other day).

And all of the recipes that I’ve spent years writing up.

And probably a whole more ton of stuff that I have yet to desperately need and therefore miss.

I’m not bawling, not just yet.

But the Voice is trying to come back.

It’s just that I don’t like losing things.

And probably I do ‘hoard’ things, ‘useful’ things.

The kind of ‘useful’ things that probably mean that my life will go on, somehow, without them.

And husband says hoarding things ‘virtually’ is just as bad a vice.

But I just get so attached to things.

And I remember them all, just like old friends.

Each pattern or recipe or photo.

They mean something to me.

There is security in saving things, in having everything that might ever be needed.

And my blanky died.

Blankies are meant to last forever.

And I certainly wasn’t big enough to be ready to let go either.

So as I have no photos, I’ll leave you with a song.

A song that kind of describes today.

(Some of the lyrics might not be kosher, however).

Oh, and this evening I just found out that a dear old friend has passed away.

It’s been a Bad, Bad, Bad Day.

Can I go to bed now?

 

(So, of course, this link won’t work either).

Loss of Self

Arum Lily in Black and White

(Can I tell you a secret?

I grieve.

There are moments when I am broken in spirit and overwhelmed by a profound sense of loss.  I try to remind myself that there are countless thousands, if not millions, of people who are in a worse position than I am but my heart won’t listen.  I put a brave face on to the outside world, set that stiff upper lip but all the time my heart is breaking.

Most people feel that it’s handing over your self-care to another person that causes a sense of loss, a sense of shame and a complete loss of dignity.  But the reality is that illness, chronic illness, will have robbed you of every last shred of dignity long before you get to that stage.  That dignity comes from our identity, our sense of self.

I cannot think of anything worse than anything to abandon self-care to a stranger, someone appointed by a remote, impersonal power through a collective, communal sense of duty to look after those unable to look after themselves.  There is perhaps slightly more grace in being cared for by loved ones but maybe that’s the point and I speak too rashly and harshly.  Think of just the nursing profession, strangers who dedicate themselves to the care of the needy and vulnerable.  Sometimes we do have to hand ourselves other to strangers, to specialists and to experts, who are best placed to help us.  I think what is needed is trust, we need to be able to build relationships, to connect and to trust, whether that person is a stranger or not, when we hand over the very last vestiges of our dignity and identity.  Perhaps the sense of shame comes only from myself.  A sense of failure too perhaps.

There is that moment where your life divides into two parts, the before and the after, that moment when a doctor or other medical professional gives you that diagnosis.  Perhaps you only hear incomprehensible medical names and terms, perhaps you only comprehend that sense of fear, dread and threat.  But what is lost, and will be lost, is your identity.

If illness only deprived us of being able to climb Mount Everest, of running a marathon every week, of being able to run six international businesses at once … well, wouldn’t that be bliss?  Few of us really would be impacted after all.  But illness, chronic illness, is so much more than that.

I don’t have that clear demarcation, I don’t have the privilege of ‘having been’, I have been ill all of my adult life and in some ways I know nothing else.  That makes me sad, sometimes I feel cheated of my potential, of being able to have a life that I choose.  I’m not one for self-pity but grief doesn’t always rationalise, it is a tidal wave of loss, from which there is no escape.

In fact, it’s when things are going better mentally, when I find a focus that I feel this loss the most strongly.  I cannot be who I want to be.  I cannot be who I am.  I disappoint and frustrate myself.  When I can see so clearly what I want to do, what I want to be and yet this mongrel-beast gets in the way, refuses to let me be, never mind achieve, I grieve.  I have found my feet in one sense but cannot crawl from the bed in the literal.

It’s absolutely crushing.

I don’t want to climb mountains, or run marathons or international businesses, I just want to be me.  All those things that I have worked so hard to achieve, I have worked so hard to find myself and to be comfortable in my skin, to have that dashed away from me, it’s heart-breaking.

And so often it’s the trivial things where I feel that sense of loss so keenly, the sort of thing that you wouldn’t ever think could really matter or be important.  Things like being able to cut vegetables properly.  But when you think about it, it is a skill and one that maybe you had to work at.  It is something small that says a lot about us, whether we cook, whether we enjoy cooking, whether we’re any good at cooking … Instead the sharpest knife becomes blunt and clumsy in uncoordinated hands, food mushes rather than slices, there is no technique and if half the pieces are of similar size, well then, that’s a miracle in its own right.  And all the while, there is that voice inside your head that tells you ‘this isn’t me’.

But it is.

Illness isn’t a straightforward, downward slope to the total loss of dignity either.  It often ebbs and wanes.  Sometimes this can be more painful; you can’t accustom yourself to a level of loss before proceeding, or descending, to the next.  What you can do one week, one day, one hour may quickly become impossible.  You can’t take anything for granted.  Each new setback is enough to make you howl.  If you had the energy.

Our sense of identity is tied so closely to the things that we enjoy.  Not being able to do the activities that we enjoy, not being able to eat the foods that we enjoy … illness leaves no aspect of us, of our identity, untouched.  But it’s not just about not being able to do the things that we enjoy, take for example my knitting.  I love knitting.  It’s one of the few activities that I can consistently manage, although in varying proportions.  But it’s so much more than just a simple activity; it’s so much more than just one of those things that I do.   It’s an expression of personality, of creativity.  It is the way that I express myself.  When a week goes by where I physically cannot knit, I feel that loss keenly.

I don’t know if illness, personified perhaps, does target those specific skills and those things that so clearly define us as us, sometimes it feels like it does, or if perhaps we just feel the loss more in those areas.  If you never had a particular skill or talent then you probably don’t notice or feel that loss so much.

I know that there are people whose memories are bad, totally fallible.  I live with one of them.  This means I have even greater responsibility as a memory-keeper, I remember my memories and those of others.  I’m known for my memory abilities.  I am a guardian of family history and stories.

No more.

I cannot remember what I did yesterday never mind last week.

I cannot remember words or dates or things that I need to do.

Someone will tell me something and I will wonder out loud how they know that.  They then tell me that I told them, just a week ago.

Behind me there is a great void of nothingness, a black hole where memories could and should exist but I remember nothing.

I feel a great sense of shame, embarrassment when faced with the reality of this loss.  Actually, it frightens me more than I care to admit.

In so many ways, this is a loss of self.  I’m losing a skill that I am proud (!) of and I risk losing my history.  In a way, I become homeless, that sense of belonging comes, in the greatest part, through memories and remembered connections.

I have a fear of losing things, my biggest fear is forgetting.  It is why I write, it is why I photograph.  I’m terrified of forgetting.  I always have been.  Memory, remembering is important to me.  And now I am faced with blank spaces, black holes and that nagging feeling that there really is something that should be in my head right now.

And it’s becoming more obvious.  It’s hard to hide your memory problems when you can’t remember anything.  I’m oblivious to what has gone before, I risk repeating things or putting my foot in it, like the example above.

Illness takes everything away from you that is precious, independence, skills, talents, memory.  There is no dignity in being ill, just a profound sense of loss.

I grieve.)

Convenient Food

Baked Beans

It was a pretty amazing invention when you think about it, probably the best thing before and since sliced bread.  A simple container that took food transportation and preservation to a whole new level: the humble tin.

Tinned food is an asset; it’s ideal for emergencies and for those moments when the rest of the cupboard and fridge is bare.  Campers swear by the stuff but caravan-ers shake their head and mutter about towing weights.  You can have vegetables in and out of season, vegetables when you haven’t been to the shops all week.  You can have a meal in minutes.

Tin food.  Great stuff.  What a convenience.

But there’s a problem.

The usefulness of a tin is in its seal.

That seal stands between me and my food.

The tin opener and I are mutual enemies.

It hasn’t always been this way, although tin openers always have a bit of a temperamental reputation.  In the years of my independence, I’ve had to make sure that I have a soft-grip handled one for the moments that my paws get flimsy.  But recently it’s descended into all-out war.  It’s not pretty.

I latch the tin opener onto the lip.

This is usually the most successful moment of the entire operation.

It goes downhill from here on in.

The next trick is to turn the wheel.

I need at least two hands to turn the wheel.

Which rather begs the question of who is to hold the handle.

You need more than two hands to operate a tin opener.

Well, I do anyway.

So I jerk into an awkward dance between turning and holding.

You need to hold tight to get the teeth to bite in.

Guess what?

I can’t.

Not anymore.

Occasionally the teeth mush into the metal, I get hopeful.

Then everything grinds to a halt again.

There is a now a minute gap broken in the seal.

I can see the food.

I can smell the food.

I can touch the food.

(Well maybe with a pinkie finger if I really wanted to try and put my uncoordinated fingers anywhere near the chewed-up metal edges).

It’s at about this point that, having spent an inordinate amount of time in this messy, stressful, exhausting business, my attention is caught by some disaster-in-progress on the hob.

I am now divided.

Do I abandon the tin which is now either spewing or spitting liquid in my direction with each painful twist and jerk as I persuade, sweet-talk, curse and manipulate the opener or, left to its own devices, sits crookedly on the worktop, slightly more bashed than when it first left the cupboard, the tin opener jutting out, jammed in the rim at some impossible angle?

Well my reactions aren’t quite what they used to be.

And neither are my decision-making abilities.

The disaster-in-progress risks ceasing to be in-progress and becoming a too-late.

I swerve, mostly mentally, between one contest and the other.

I can’t cope!

I am overwhelmed.

I, the tin and the rest of the food need rescuing.  Urgently.

Having gone through this very exhausting and dangerous process several times in recent months, I have a new strategy: I don’t open tins.  That’s husband’s job now.

I admit defeat.

I give up.

Although not graciously.

But then there was a glimmer of hope.

Some food tins have ring pulls.

I can open ring pulls.

I am triumphant in my new found talent, a moment of victory and conquest.

I need two thumbs to lever up a ring pull.

This means that I need to clutch the tin, which suddenly has acquired the animate ability to wriggle, between my two wretchedly weak paws and still have enough length and stretch left to manipulate my thumbs under what transpires to be a stubborn, stiff piece of metal.

Sometimes my thumbs win the fight.

Sometimes I have to adopt something that proves that I am indeed a higher being: a tool.

I grab the nearest thing that seems vaguely appropriate, a dinner knife or a teaspoon.

The ring pull is stubborn but so am I.

And I am armed.

With a teaspoon.

The fight is won.

The ring pull is levered up, victory is achieved!

There is a minute gap broken in the seal.

I can see the food.

I can smell the food.

I can touch the food.

Like me, do you get a feeling of having been here before?

And that is as far as I can get.

The pride and jubilation of a battle won is quickly swept aside as the tin wins the war.  Again.

I am stubborn but I know when I am defeated.

I am defeated.

If I want to eat tonight, I will have to surrender; I will have to give the tin over to more capable hands.

Bitterness is not something that I easily succumb to.  Fortunately.  But there’s not much fun in being beaten by a tin of food.  And sometimes I’d just really like some baked beans.

Tinned food, hey?  What a convenience!

Welcome to the Real World

Swan's Head with Dripping Beak

When speccy spoke of pacing the other day, my entire being sighed and nodded knowingly in agreement.  You see, pacing is something of a ‘buzz’ word in chronic illness.  Although it’s not some magical cure-all or panacea, it does rather let the ‘experts’ off the hook.  The responsibility is handed firmly back to the patient, they are to manage their own illness, it is up to them.

Whilst I firmly believe that self-awareness and self-management are important, if not vital, components of maturity, of adult life, this doesn’t quite seem fair.  There was a reason why ‘experts’ were invented after all.  To be left, abandoned, to your own devices can be isolating, frightening and threatening.

It’s sometimes said that the best gift you can give the chronically ill is comprehension.  Support and understanding are absolutely crucial and they have to come from external sources.  Yes, as individuals, we can offer ourselves support and understanding but it’s not the same.  In fact, can any individual really generate and sustain support, understanding, belief, appreciation or acceptance if there is none forthcoming from external sources, the community around them?  (And when someone is chronically ill, can they really physically support themselves?  If they could, they wouldn’t be the ill ones).  This would require almost unfathomably ridiculous levels of self-belief and self-confidence.  I don’t think many of us have those.

Besides, chronic illness eats away at your self-belief and self-confidence.  It destroys value systems.  Even if you never, ever doubted yourself before, it will make you doubt now.  Sometimes you will think that you’re going crazy.  That’s why external sources of belief, support and understanding are so important.  No man is an island, apparently.  We don’t need flattery or lying to, we simply need to be acknowledged, for our illness to be acknowledged.  Or better still, understood.  Appreciated even?

Perhaps, they, those ‘experts’, feel that this approach is temptingly flattering.  You are the expert, you know yourself better than anyone and the nature of your illness too.  You are the expert.  Empowerment in action, another favourite ‘buzz’ word of our times.

However, it carelessly disregards the reality, how the dynamics of self, relationships, community, society really work.  No man is a self-actualised island existing in splendid isolation, an unconnected self on a planet of unrelated life.  As if such an ideal were even possible.  Or healthy.  We humans are cities, places buzzing with connections, with a strong sense of past and a need for a planned, controllable, reliable future.  We have habits, customs.  We are often living to the full extent, if not beyond, of our resources.

When we fall ill, we bring a lot of baggage with us.  Our own expectations, hang-ups, complexes, fears and prejudices.  As well as those of everyone else too.  We cannot be expected to become a self-actualised island in the face of such odds.  Nor should it be required, we are cities after all.

(As a side note, isolation is an often recognised and accepted issue for the chronically ill, so it seems a little unwise to propagate it).

There are other ways too that pacing is fundamentally flawed.

Another situation where the term ‘pacing’ is popular and enthusiastically adopted is in sport.  (If there couldn’t be more difference between these two groups of proponents!)  Top athletes, marathon-runners, you name it, they all talk about pacing, it’s a wonder-word to them too.

However athletes do not exist in isolation.  They are part of a team.  And not just any team either, these aren’t necessarily just their loved ones who for the chronically ill will make up the bulk, if not the entire population, of a support team. Oh no, the athlete is surrounded by ‘experts’.  Whilst it is recognised that he knows himself and his abilities best, he turns to external sources to help manage and advance, he knows that he cannot do it alone.  There will be a coach providing one-to-one support, usually someone who has a wealth of experience and knowledge in a particular sport.  The best coaches know the ropes and they know them inside out, upside down and back to front.  They have the inside story on each challenge that an athlete will face.  And they know their athletes just as well.  They know how to get the best from their athlete, how to maximise their potential, when to push’em and when to ease off.  But these days, it isn’t just the coach who makes up the support team.  These days, there is a vast network of ‘experts’, professionals in diverse fields all bringing their knowledge and experience to bear, to allow the athlete to achieve his potential, there may be nutritionists, physiotherapists, masseurs, sport scientists, doctors, psychologists, administrators, legal experts, public relations specialists … the list goes on.  No athlete is an island.

So with all this support, knowledge, expertise and belief propelling an athlete forward, does pacing actually guarantee a win?  Well, think over some of the interviews you may have heard with athletes after some event or other.  You will hear them talking of peaking too early, of having had a bad day, of the weather being against them, of the altitude being unfavourable, of having two events too close together, of having had troublesome journeys or connections.  Even with all these experts behind them, even with all their own self-belief and training behind them, pacing is fallible.  Highly fallible.  It is not a science.  We humans generate too many variables and respond so differently and unpredictably to situations, even familiar ones.

One Swedish furniture company apparently tests all of their new sofas with a special machine which simulates someone, a rather large someone, jumping on the sofa countless times.  They are measuring endurance.  When those figures are produced, they can then guarantee their furniture for a specific period.

What does this have to do with pacing?  Well, the essence of pacing is endurance.  And how do you measure that in humans?  We are not identical sofas manufactured to exacting standards.  (In fact, I’m pretty sure that some of us feel like second-hand sofas anyway).  But it means that the test is no longer fair because not all the sofas can and will pass.  And think of that old relic in your sitting room, just because it’s rather old and sorry, are you going to throw it out?  Or will you overlook its faults, it weaknesses because it’s deliciously comfortable and been part of your family story for such a long time?

There are other problems too when it comes to measuring endurance in humans, not only are we all built differently but we’re not tested equally either.  The tests that a human faces, even in normal everyday life, are random.  There is no uniform test.  And the tests that humans face are not necessarily designed to be passed with flying colours.  And how do you measure endurance when humans have the unpredictable trait of responding differently in the same circumstances?

Endurance is really the baseline of pacing.  Pacing requires you to establish what you are normally capable of, what you can usually endure.  Once you have established this elusive baseline, you can pace yourself, not exerting yourself beyond this threshold and therefore not exacerbating your condition.  Eventually you will be able to build on the baseline, increasing gradually in baby-steps increments your abilities, your endurance, your baseline.

There is some truth, some science behind this.  But even experienced athletes can find that their baseline fluctuates and that sometimes there are just ‘bad days’.  How much more so for the mere mortal struggling with a chronic illness!

Endurance, I don’t think, can be quantified and measured in humans.  Endurance seems to be one of those qualities that meanders between the physical and the psychological.  There are few things that are clear-cut, black and white where humans are involved.  And whilst an athlete knows that they can run this fast for this long or whatever else their discipline requires of them, a purely physical endurance, how predictable or reliable is chronic illness?  This athlete is an individual with high levels of self-belief and self-confidence, yet whilst he may be able to endure physically, the psychological can knock him for six.   Chronic illness does not neatly exist only in the physical, or mental, there is a great deal of psychological.  We bring all that baggage with us, remember?

So if endurance cannot be quantified and established, fixed at a set rate even one individual, how can pacing really be expected to work?

But then it gets more complicated.  We humans don’t exist at some monotonous baseline; we peak and relax, physically and psychologically.  Our lives are varied.  Even if we had that baseline fixed and we could measure everything we did against it, is that really how humans live?  Just because we are ill, even house- or bedbound, we are humans with a strong sense of will.  We want to do things.  We live in a society where our value is dependent on activity.  We measure success by what we do, how much we do.  There are things that must be done.  Life doesn’t stop when you become ill.  There are still all of these everyday responsibilities to be taken care of.  And there are times, when we just desperately want to do something, maybe to alleviate some of the boredom and frustration of being so ill so much of the time, maybe it’s because we just want a glimpse of our old lives.  We rarely say no.  We’re not programmed to say no.  And so our pacing suffers, even if existed in the first place.  Real life continues around us and continues to have expectations of us.  We also have expectations of ourselves too.  Modern society is not renowned for its measured pace.  And there isn’t much allowance given for the chronically ill.  Pacing goes out the window, you have to live.

Whilst Chronic illness can be boring and frustrating, it isn’t monotonous.  Whilst real life continues to throw challenges us, things that we must do regardless of our health or energy levels, chronic illness itself doesn’t exactly help matters either.  Few chronic illnesses are predictable.  They are not reliable.  Most of them aren’t even quantifiable.  So how can you apply pacing to the untameable?  The worst of chronic illness is never knowing quite how something will affect you until it’s too late.

Pacing allows a veneer of delusion that someone is in control.  That the beast of chronic illness can indeed be tamed, be domesticated and invited into polite society.  It would be a comforting notion if it wasn’t so obviously false.  But yet countless patients dutifully try to implement the impossible, they try to pace themselves, in an almost vain hope of recovery.  If recovery or remission does occur, it rarely seems to be anyone’s hands.  There is no success guaranteed with pacing and yet the patient has had to take full responsibility for the management and successful outcome of their illness.  Is this failure or just stupidity?

I don’t think that pacing can be that panacea; I don’t think it is the solution.  There is an awful lot more involved in humans, in illness and in real life.  Pacing is the equivalent of a highly restrictive calorie-counting diet; it’s punitive and doesn’t take into account those ups and downs, the feasts and famines of real life.  Oh, and they haven’t managed to invent the calorie either.  Pacing is a farce.

We need to be realistic.  We do need to recognise our personal limits and accept that these will often vary.  We need to recognise and accept that if we choose to participate in one activity then it will often be at the cost of something else.  We cannot have everything.  Sometimes we get a look at the cake but it’s rare that we get to eat it.  We need to accept these things for ourselves, to reject all the baggage and activity-dependent value systems that we were brought up with and are surrounded by still.  But we are not islands; we need the people around us to do the same too.  We need their support, belief and understanding in order to live, to be allowed to live at our own pace.

My Two Proofs

Bug - (Cinnabar Caterpillar)

‘Complimentary’ or ‘alternative’ (the term you choose to use probably reflects your views) healthcare seems to be a great divider of opinion in these modern ages.  The rigid disciples of Science believe only in its apparently concrete, modern and proven theories dismissing other views as quackery suitable only for misguided ignoramuses stuck in the Dark Ages of Folklore.  They forget that folklore is the very foundation of their own pride and joy, its original springboard into modern terminology and that in fact Science and Folklore are still tightly entwined bedfellows.  Aspirin anyone?

Personally I find modern Medicine, much like all branches of Science, a little rigid in its understanding and a little too keen on pigeonholing.  I’d rather treat something holistically than to focus on one symptom and dose it up on chemicals.  Medicine prides itself on the physical, only accepting the tangible proofs of illness.  It struggles to explain and cope with conditions like ME.  And what is pain?  Physical, psychological, psychosomatic?  All or none?  I sometimes find Medicine too black and white.

I’ve used various treatments and systems of medicine before for various ailments, I respond better to them with no side effects which to me is a clear advantage.  There’s less risk of overdosing too, comforting.  One of the things that I regularly return to is homoeopathy, a quackery that some bristle up with a vengeance at the idea of.  Each to their own, I’ll leave you to your opinion and decision so leave me to mine likewise.

They often claim that any positive effect homoeopathy may accidentally have on a patient is simply a placebo response.  If you give a human any pill-like object to take, he will magically believe himself better.  I don’t know what this says about human intelligence.

I have two proofs, conclusive to my way of thinking at least, that homoeopathy works for real and I offer them up to you now:

  1. My husband.  He loathes all medicine with a passion whatever its origin, suffering is a noble art and the only way to deal with illness.  He won’t take painkillers for a headache because it’ll ‘go away eventually’.  In the meantime he can’t do anything and is a total pain to live with.  I dose him appropriately regardless, husbands don’t know best in this instance, including with homeoepathic remedies which just like ‘standard’ or ‘orthodox’ or ‘Western’ treatments will do nothing. and never have done  The thing I love most about homeopathy is the symptom pictures that each remedy indicates, more than just your fever but the time it gets worse and often small details about your personality.  My husband’s go-to remedy when he has a lurgi has the following description included: ‘a bear with a ‘sore head’ who is irritable and resentful of being questioned or fussed over’.  Hmm.  That’s him to a T.  And do you know what?  That remedy works every time.  Even though he still refuses to believe so.  Placebo effect?  Not if he could help it.
  2. The family dog.  The dog has even less intelligence than the husband and is normally completely oblivious to having taken a pill (I drop them in his water bowl to dissolve).  So I don’t think placebo effect is therefore possible there either.  In the past, when I was a child, we had a rescue dog who we treated successfully for separation anxiety and the current incumbent was dosed for another psychological condition for which modern Medicine offers no treatment or cure for, especially not for four-legged patients, grieving.

And there are my proofs.  If it works on the stubborn and the ignorant, it has to have worked.  In any case, life was better for all concerned after dosing which is the essence of Medicine anyway.

The Oh-So-Long Symptom List

Neurological Signs and Symptoms:

  • Inconsistent central nervous system function
  • Vertigo and disequilibrium, for example a sensation that your surroundings (or you) are spinning wildly and vertigo may also be expressed in a milder form as an inability to watch TV or to read (or knit!)
  • Temperature dysregulation
  • Poor tolerance for hot or cold environments
  • Hyperacusis (sensitivity to noise)
  • Photophobia (pain/relapse on exposure to light)
  • Pain and pressure at the back of the head (where the head meets the neck) and behind the eyes
  • Visual disturbances such as blurred vision, blacked-out vision and wavy visual field
  • Sensory storms‘ (while conscious)
  • Fragmented sleep
  • Difficulty initiating sleep
  • Lack of deep-stage sleep
  • Disrupted, chaotic or reversed circadian rhythms
  • Extreme intolerance to vibration or movement
  • Sudden loud noises can also cause a startle response (flushing and a rapid heartbeat)
  • Tinnitus
  • Simple partial seizures which do not involve loss of consciousness but produce altered sensations, perception, mood or bodily sensations; somatosensory seizures, autonomic seizures, focal motor seizures, auditory seizures, visual seizures
  • Complex partial seizures: episodic dysphasia/dysphagia (incomprehension of speech and inability to speak), olfactory hallucinations (smelling curry, for example, wherever I am)
  • Overload phenomena
  • Unrefreshing sleep (waking up feeling worse than when you went to bed)
  • Hypersomnia
  • Dysania (doesn’t that sound like a yoghurt or some branded water?)
  • Sluggish focus (visually), an inability to focus or accommodation difficulty (difficulty switching from one focus to another)
  • Vision reversals
  • Vision clouding
  • Intolerance of extremes of hot and cold weather
  • Changes in barometric pressure can cause night sweats and spontaneous sweating during the day
  • Insomnia, migraines, irritability or generally ‘feeling off’ a day or two before the weather changes
  • Changes in temperature or humidity can cause stiffness or increased aching or pain in the muscles

Vascular and Cardiovascular Signs and Symptoms:

  • Chest pressure, heart pain and a fluttering/straining heart
  • Postural Orthostatic Tachycardia Syndrome
  • Feet burning painfully and turning blue/purple on standing (Raynaud’s phenomenon)
  • Pain/discomfort/poor digestion following meals
  • An exacerbation of symptoms on orthostatic challenge (maintaining an upright posture) beyond certain limits. (Lying down markedly improves symptoms for M.E. patients).
  • Orthostatic light-headedness or  blackouts
  • Oedema (swelling of the hands and feet)
  • Extreme pallor (usually just before or during a relapse)
  • It has never been investigated whether I suffer with more specific problems to do with low blood pressure, high heart rate, sleep bradycardia, arrhythmias or reduced circulating blood volume

Cognitive Signs and Symptoms:

 

  • Word-finding difficulty, incorrect word selection (paraphasia) is common, such as using the wrong word from the right category or using a word that sounds similar to the correct word but has a different meaning
  • Commonly used words become hard to retrieve
  • ‘Scanning’ or disjointed speech
  • Speech reversals
  • Difficulty comprehending speech or delayed speech comprehension
  • Handwriting changes (this waxes and wanes with the severity of illness)
  • Difficulty writing or comprehending text
  • Difficulty with even basic mathematics (dyscalculia) (although somewhat difficult to prove in someone who has trouble counting higher than thirty!), an inability or difficulty to do simple additions and other calculations, to count money, add up columns etc
  • Difficulty with multi-tasking and simultaneous processing
  • Impairment of concentration, maintaining a reasonable level of concentration on a task for even a short period of time may become extremely difficult and sometimes impossible, there is a need for mental micro-rests
  • Difficulty with spatial perception, for example a loss of co-ordination or clumsiness, difficulty in judging distance, placement and relative velocity (caused by proprioception dysfunctions, proprioception being the perception of stimuli relating to your own position, posture, equilibrium, or internal condition)
  • Extension or quick rotation of the neck can cause dizziness (also due to proprioception dysfunctions)
  • Difficulty with sequencing, an inability to look up words in a dictionary, organise files or look up phone numbers
  • Difficulty  with memory including: making and consolidating new memories, recalling formed memories, and with immediate and delayed visual and verbal recall (e.g. facial agnosia); short term memory problems may lead to forgetting what they are doing to such a severity that I am unable to finish a sentence
  • Inability to learn new tasks and forgetting how to perform routine tasks
  • May need extra sensory cues to complete tasks, for example having the light on when before the task could be done by touch alone, or can understand a conversation face-to-face but not over the phone
  • Cognitive slowing
  • Difficulty with visual and aural comprehension
  • Difficulty following oral or written directions
  • Trouble distinguishing figure from ground and speech comprehension difficulties.
  • Word, letter and short term ordering problems, for example; transposition – reversal of letters or numbers, words or sentences when speaking or writing (pseudodyslexia)
  • Agraphia, inability to locate the words for writing
  • Problems with reading (alexia) or word blindness; I can still read but what is read is not comprehended and cannot be compared with known information already stored
  • Despite actively listening, the information simply does not register at all or must be repeated several times before it registers
  • In speaking, my syntax is askew often
  • Speech comprehension is delayed which can result in long pauses, interruptions, mistiming of responses and apparent non sequiturs
  • Difficulty or confusion with following timetables or keeping scheduled appointments
  • Loss of the ability to block out extraneous and unwanted information and noise
  • Loss of the ability to distinguish noise from required information and tend to shut down all intake after minimal prolongation of the information signal
  • An exaggerated response to even small amounts of additional input or stimulus (light, noise, movement, vibration) is common, causing incoming messages to become scrambled or blurred resulting in distorted signals and odd sensations (ie. low level seizure activity)
  • Even very low levels of light or noise etc. can also cause an exacerbation of other symptoms, or of the severity of the illness generally
  • Altered time perception (losing time), feeling ‘spaced out’ or ‘cloudy’ or not quite real somehow
  • Abstract reasoning dysfunction; difficulty organising, integrating, and evaluating information to form conclusions or make decisions
  • The brain becomes unable to maintain wakefulness; there can be a difficulty in maintaining full consciousness for more than a few seconds, minutes, or half-hour periods at a time
  • Volitional problems: difficulty starting or stopping tasks, or switching from one task to another (a neurological dysfunction where the body does not respond appropriately, or quickly, or without difficulty, to the minds commands)
  • Agitated exhaustion (neurological in origin)
  • Emotional symptoms include: mood swings (emotional lability) – crying easily etc. or intense emotions such as rage, terror, overwhelming grief, anxiety, depression and guilt, there can be an emotional flattening or situations may be erroneously interpreted as novel (due to prefrontal cortex dysfunction)
  • Emotional symptoms in M.E. tend to be linked to exacerbations in physical symptoms, there are often not environmental triggers
  • A worsening of symptoms (including cognitive function) with cognitive exertion beyond a certain level

 

There is often a marked loss (20 points on average) in verbal and performance IQ (fortunately I never have had to sit an IQ test)

Greater difficulty with auditory comprehension than visual is common (ie, with these ears of mine, I’m stuffed)

Digestive Signs and Symptoms:

  • Oesophageal spasms (felt as extreme pain in the centre of the chest that sometimes radiates to the chest or mid-back) or oesophageal reflux (heartburn)
  • Difficulty swallowing (or an inability to swallow)
  • Great thirst or increased appetite
  • Food cravings or lack of appetite
  • Inability to tolerate much fat in the diet (gallbladder problems)
  • Changes in taste and smell
  • An increased sense of smell or bizarre smells (for example, the week I could smell curry everywhere, it was very odd)
  • Strange taste in mouth (bitter, metallic)
  • Multiple new food allergies and intolerances (I can’t eat garlic anymore.  And cucumber and watermelon are problematic).
  • Bloating, tenderness, discomfort
  • Abdominal pain
  • Nausea
  • Indigestion
  • Constipation
  • Alcohol intolerance is common (this also waxes and wanes but can be frustratingly unpredictable)
  • Feeling ‘poisoned’ and very ill

Endocrine and Neuroendocrine Signs and Symptoms:

  • Loss of thermostatic stability – suddenly feeling cold in warm weather, recurrent feelings of feverishness or chills or hot flashes particularly involving the upper body
  • Low-grade fever may occur following exertion
  • Temperature fluctuation throughout the day (unproven abnormal temperature but the sensation is there)
  • Cold hands and feet, sometimes on only one side
  • Sweating episodes (profuse sweating, sometimes even when cold)
  • Swelling of the extremities
  • Loss of adaptability and worsening of symptoms with stress due to endocrine dysfunctions
  • Hypoglycaemia or hypoglycaemia-like symptoms (problems with blood sugar regulation/low blood sugar)

Muscular, Pain, Exertion and Physical Activity Signs and Symptoms

  • An exacerbation of symptoms with physical activity beyond a person’s individual limits, and a worsening of the illness generally (etc.) with continued overexertion
  • Severe muscle weakness (paresis) or paralysis
  • Muscles will often function normally to start with, but pain and weakness (or paralysis) develop after short periods of use and then take 3, 4 or 5 days (or longer) to resolve (normal muscle recovery is around 200 minutes
  • Problems arise from sustained muscle use – it is a pathologically slow or impaired recovery of muscle after exercise (metabolism of the muscles), therefore I may be easily able (for short periods) to lift something moderately heavy one or two times, but be unable to lift something very light many times
  • Muscle weakness/paralysis affects all muscles/organs, including the heart, eyes and brain
  • Dyspnoea with overexertion
  • Erratic breathing pattern
  • Loss of the natural antidepressant effect of exercise
  • Inappropriate signs of immune system activation can be brought on by overexertion (i.e. flu-like symptoms)
  • Persistent coughing and wheezing
  • Worsening of symptoms generally caused by a hypersensitivity to light, sound, vibration, movement, temperature, odours and/or mixed sensory modalities
  • Muscle weakness and paralysis (affecting all muscles including the heart, eyes, digestive system etc.)
  • Muscle pain, twitching and uncontrollable spasms
  • Difficulty breathing and air-hunger
  • Difficulty swallowing or chewing
  • Paraesthesia
  • Polyneuropathy
  • Myoclonus
  • Onset of a new type of headaches, severe or pattern of headaches is common, often associated with neck rigidity and occipital pain (pain/pressure felt at the base of the skull, the top of the neck) and/or retro-orbital eye pain (pain behind the eyes) and also sometimes pain behind the ears (or one ear).
  • Sinus, pressure or tension headaches (dull continual headaches which are not actually caused by anxiety as the name may suggest)
  • Hypoglycaemia headaches (generalised prickly ache over the top of the head) (I had wondered what the nice prickly headache thing was about)
  • Sharp transient ear pain
  • Deep itching in the ears (I just learnt that could be a symptom today!)
  • Significant (can be extremely severe in M.E) myalgia (pain) in joints is often widespread, especially knees, hips and fingers; sharp, shooting, burning or aching pain
  • Gelling (stiffness) in the joints that develops after holding a position for awhile
  • Aching in the joints
  • Gait abnormalities and a difficulty with tandem gait
  • Inability to form facial expressions leading to a ‘slack’ facial appearance, almost Parkinsonian
  • Spasms of the hands and feet which can lead to ‘clawed’ deformities
  • Spasms in the neck which cause the head to twist to one side
  • Some cogwheel and leadpipe rigidity
  • Slight hesitation in movement
  • Severe spike-like pain, usually in the main muscle mass in the leg; extensors or flexors,  commonly described as feeling as though a nail or a knife had been stuck into the area
  • Formication (another ‘new’ one learnt today whilst doing that, whilst many languages use ‘ants’ to describe pins and needles, I am often very aware of a different sensation to pins and needles, it does feel like being bitten or stung by ants, a burning, itching and crawling sensation)
  • Allodynia – for example, the weight of the bedcovers becomes ridiculously heavy and painful
  • Problems with nails such as vertical ridges, bluish nail bed, brittleness
  • Marked weight gain or loss (often independent of dietary changes) (particularly as a teenager)

 

Immunological Signs and Symptoms:

  • Lymphadenopathy
  • Recurrent flu-like symptoms (general malaise, fever and chills, sweats, cough, night sweats, low grade fever, sore throat, feeling hot often and low body temperature)
  • Very severe throat pain, scratchiness and tenderness which often worsens with exercise, exertion or before relapses
  • Increased or decreased susceptibility to secondary infections, a tendency to catch either every virus going around or to ‘never catch anything’ depending on whether the immune system is under- or over-active (which changes dependant on which stage of the illness the person is in)
  • Infections also last longer, can be more severe and occur more frequently and may also cause relapses either concurrently or just after the initial infection
  • Reactions to chemical smells
  • Chemical sensitivities may occur to indoor and outdoor chemical air contaminants; can produce allergic reactions although not all chemical sensitivities are IgE mediated, may also cause an exacerbation of other symptoms
  • Worsening of existing allergies and/or new severe sensitivities/allergies/intolerances to many varieties of food (and food additives) and to airborne allergens
  • Hair loss and poor quality regrowth
  • Skin rashes
  • Dry and peeling skin
  • Spontaneous bruising (aha!  I have long been plagued by a Murphy’s Law state of bruising, I rarely seem to come up in bruises when I bash myself but I find random bruises that have no apparent cause all the time)
  • Flushing of face (my face is very red most of the time actually, I can’t use blusher anymore)
  • Finger pads may be atrophic so that the fingerprints are hard to see, skin may become red and shiny (my hands often look like I’ve spent far too much time in a bathtub)

Oral Signs and Symptoms:

  • Dental decay and periodontal disease (gum disease) are much more common than in the general population
  • Frequent canker sores (I thought that this was something to do with horses, but hey!)
  • Temperature sensitivity in the teeth
  • Pain in the teeth
  • Tooth-hypersensitivity pain

CO-MORBID ENTITIES: 

  • Secondary or reactive depression (as with any other debilitating chronic illness) (actually primary depression, it commenced before ME but they don’t get on well)
  • Irritable Bowel Syndrome
  • Raynaud’s phenomenon (poor circulation) (symptoms of but never been investigated)
  • Carpal tunnel syndrome (weakness, pain, and disturbances of sensation in the hand) (possible as have symptoms of but never been investigated)

It sucks, doesn’t it?

(Information has been mostly drawn from the highly information Hummingbird website, many thanks to its authors).

That Mongrel-Beast Actually Causes Quite a Few Problems

Donkey Love - Two Donkeys 'Hugging'

My usual technique for dealing with illness is to ignore it.  Well, it might just go away.  And I’m used to blaming the psychological for a lot of my problems, for example, I say, ‘I’m lazy’ or ‘I can’t be bothered’.  But I’m growing in awareness, both of my main physical condition (ME) and of myself.  I know now that I’m not lazy but I’m still reluctant to take on board the fact that perhaps that mongrel-beast does actually cause me quite a few difficulties.  I suppose, perhaps, it partly goes back to that very screwy idea of ‘deserving to be ill‘.  I just tell myself, and anyone else, that ‘I’m just making a fuss, it’s nothing really’.  And that’s how I see it and how I live my life.

But the problems don’t just go away if you try to ignore them.  They’re still there.  Misunderstood, mislabelled, mismanaged.  It’s not a good recipe for success.  I have to face up to the fact that the mongrel-beast is ever present, that all those queer symptoms that irritate  frustrate and confuse are probably its fault.  Others, unfortunately, have just become my ‘normal’, I’m so used to feeling one way or another, one thing or another, that I scarcely appreciate that most people don’t actually feel that way, or ‘thing’.

I don’t like ignorance.   I do agree that knowledge can be power.  It can inform and educate.  And that’s what is desperately needed in these neurological conditions and ‘invisible’ illnesses such as ME.  It would be hypocritical of me to continue denying its existence in my life.  I cannot preach the need for awareness when I am steadfastly refusing to be aware.

Awareness does have its downsides, of course.  It can overwhelming,  frightening.  It’s almost like that moment when you first receive a diagnosis (not that ever happened in my case), the ground becomes unsteady and you find yourself confronted with a whole new reality, future, lifestyle … everything.   This condition is all-pervasive.  Being an ostrich doesn’t change that.

I preach also for tolerance, and I don’t necessarily use the word in the modern sense of ‘permissive’, for me, it’s a generosity of spirit and understanding and appreciation towards your fellow man.  How can I expect others to be tolerant when I am so hard on myself?  Again, it would be totally hypocritical.  I don’t do hypocritical.

Something has to change.  I have to change.

I have to face up to reality, to be tolerant to myself, to offer myself the understanding and appreciation that I so willingly give others.  I don’t make excuses as if they have no responsibility for their actions but I do understand and appreciate that there are, at times, extenuating circumstances.   I don’t get upset with you personally when your behaviour is generated, triggered by illness, stress or something out of your control.  I just ask that you acknowledge it and, if necessary, apologise afterwards.  Do I do the same for myself?

I preach also inclusion.  I don’t think that illness or disability should ever be cause for exclusion.  Sure, you may have to do things differently or a different pace, but I don’t believe that illness or disability is ever a write-off.  Yet, I hide my own problems.  From shame?  Perhaps.  Because I want to exist in the world on the basis of other terms, preferably my own and not this mongrel-beast’s?  Perhaps.  It’s kind of complicated!  But inclusion means allowance and I’m not allowing myself to be or to show the actual reality.  I am discriminating.  That is not tolerance.  I am judging.  That is not kindness.

I cannot hold myself responsible for something beyond my control, I cannot take responsibility or blame for a life or illness that I never chose.  Or even probably provoked.  I have to be forgiving.

And yet, even as I come to appreciate the all-encompassing nature of this mongrel-beast, I can also start to differentiate, between me and it.  I can see more clearly who I am and what the illness is.  Believing, understanding and appreciating actually frees me up.  I can be true to myself.  Just in difficult circumstances.  I don’t have to be the illness, I can be myself with an illness.

And most important?  I can start to take myself seriously.  Sometimes, it feels like no-one has ever taken me seriously.  And perhaps as a child, that does have to start as an external process, someone has to believe in you.  But as an adult, it’s up to me.  The first step is that I have to take myself seriously.  Then it’s up to everyone else.  Again, there’s that hypocrisy.  I cannot expect others to take me seriously when I am not taking myself seriously.

So today, I compiled a list of my symptoms, all the ones that I have ever had thanks to mongrel-beast.  It was hard work, not least because mongrel-beast is very keen on cooperating on such cognitive tasks (it doesn’t even like spelling or typing) and also because I had to face reality.  Reality is not the nicest thing in the world.  It’s kind of like looking in the mirror with your glasses on.  Not good.  But you can’t always avoid it.

I’m going to post the list separately because it is rather long and no, I really don’t expect any of you to trawl all the way through!  (Especially as I rather suspect, it’s full of mistakes and typos). Instead, it’s going to be a sort of testament.  A reality check, if you will.  For myself mainly.

I worked through the symptoms section on the Hummingbird website, it’s thorough and comprehensive.  I could say that I have learnt lots of new words but the reality is that I have immediately forgotten them.  I’ll try to link definitions to some of the stranger (mostly Latin-ish) terms.

I’m also quite glad that I went with bullet points and not numbers, it could have got a little (actually, very) frightening!