No spoons (or forks) for me…

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A while ago I wrote about the history of “spoons” – the metaphor people with fibromyalgia use to explain how people with chronic pain allocate their limited amounts of energy.  Today I want to go into a bit more detail to explain the idea, AND tell you why it doesn’t really work for me.

The concept of spoons goes a bit like this (and I’m not a ‘spoonie’ so sorry if I get it wrong); different activities take different amounts of spoons, or energy, and in the same way that you only have so many spoons in your kitchen draw, you also have to decide how best to allocate your energy throughout the day.  Let’s say an upcoming day looks like this (with the spoons you’ll need in brackets): shower (1); walk dog (2); write letter for work (1); emails for work (1); vacuum house (2); clean bathrooms (1); make lunch (1); write report for work (3); make dinner (2); watch TV (1).

On a good day, you’re going to get through all 15 spoons.  On a not-so-good day, however, you might feel like you only have 10 spoons worth of energy – you will have to prioritize.  You might decide work is a must, so those 5 spoons HAVE TO get done, so you lose some of the chores to make it happen.  Or else, you might have organized people to come to dinner, so the cleaning and dinner prep are going to be what you keep, but you’ll drop some of the work elements and the dog might have to wait until tomorrow.  Now imagine it’s a really bad day, and you only have 5 spoons to spend…

The reason why the analogy doesn’t work so well for chronic migraine is because migraine is a different kind of beastie… if you have a flat-out-almost-unconscious-with-pain style migraine, then you have NO spoons to use… and no forks to give when it comes to what should be a priority… you’re not getting out of bed for anything or anyone… you just can’t.

If the migraine is bad, but not super-terrible, then it’s still not about energy levels.  It has more to do with various pain-triggers.  Vacuum?  Nope – too noisy.  Walk dog? Probably not – the exercise is too much too soon.  Make dinner?  Ahhhh, no – the smells might trigger another vomiting attack, and besides you’re not hungry.  Work for the boss?  No can do – you’re not going to be able to sit in front of the computer and draw down on your cognitive abilities… yet.  So, that leaves showering and cleaning the bathroom and maybe watching TV (assuming it’s not too loud or flashy).

So, you see, the spoons model doesn’t work too well for me as a way of explaining why my energy runs out faster than others – it’s complicated by the tongs and spatulas tangled up in the energy-drawer.

While reading The Brainless Blogger, however, and her post about productivity and chronic illness, I realized there’s another way.  As the mermaid-haired-blogger points out – we all get 24 hours in the day.  She explains the distribution of time in her own way, and it’s definitely worth a read, but here’s my summary of what’s going on for me…

A ‘normal’ person might sleep for 8 hours, work for 8 and use the last 8 hours to do chores, relax or do creative pursuits.  All up, that means they have 2/3rds of the day to be productive, and 1/3rd to be at rest.  A ‘sick’ person, however, needs the same 8 hours of sleep, but knows they can’t pull off an 8 hour work day, so they might aim for 4.  Similarly, there are limitations on how many chores and other activities they can get done before they run out of steam, so again, they might aim for 4 hours.  In between those up-and-about activities, they will potentially need to rest, nap, or just slow down.  This means that the proportions are reversed; 1/3rd of their day is productive, whilst 2/3rds are required for rest and rehabilitation.

It means that even on our good days, we’re way behind others in what we can produce.  It makes us sad and frustrated, but we’re doing the best we can do.  What’s important to remember, is that if you are on the more ‘normal’ side of the ledger – we all have the same amount of AVAILABLE time, but you have access to a lot more energy, and therefore PRODUCTIVE time than we do – so, without sounding snarky; don’t take that productivity for granted and don’t judge us when we can’t keep up. 

For those of you on the ‘sicko’ side of the equation – keep doing the best you can – you’re doing great.

Take care, Linda xx


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22 responses to “No spoons (or forks) for me…”

  1.  Avatar
    Anonymous

    I love those diagrams!!

    Liked by 1 person

    1. The Mindful Migraine Blog Avatar

      thanks! hope they help, L xx

      Like

  2. Mel Avatar

    Those pie charts are so helpful–thank you! I constantly have to remind my Energizer Bunny-brain that it’s normal and healthy to need extra rest!

    Liked by 1 person

    1. The Mindful Migraine Blog Avatar

      I’m with you – I tend to push trough and then wonder why I’m crashing… some days are better than others, so there’s no hard and fast rules… but being kind to ourselves is sooooo important! xox

      Like

      1. Mel Avatar

        Agreed!

        Liked by 1 person

        1. The Mindful Migraine Blog Avatar

          🌞

          Like

  3. Writer McWriterson Avatar

    Oh gosh, this really hits home. Migraines have no timetable—they can strike at any time, day or night. When they do, I sometimes feel depleted for days.

    I love the spoons analogy! I had never heard of it before.

    Liked by 1 person

    1. The Mindful Migraine Blog Avatar

      I only learnt about it through other chronically ill people… it’s not normally a migraine thing… but it does help remind me and others that I can’t give as much as I used to! Have a wonderful weekend, L xx

      Liked by 1 person

      1. Writer McWriterson Avatar

        I hope you had a wonderful weekend! 😘

        Liked by 1 person

        1. The Mindful Migraine Blog Avatar

          Thank you lovely – it was a bit of a sick weekend… just when I think I’m getting better, it suddenly gets worse… never mind – onwards and upwards! (hope you’re OK too) xox

          Liked by 1 person

          1. Writer McWriterson Avatar

            I’m so sorry to hear that.
            Sending you lots of love because I’ve been where you are. If you want to vent, I’m always here.😘❤️

            Liked by 1 person

            1. The Mindful Migraine Blog Avatar

              It’s a catch 22 – when I vent I lean into the frustration and pain… it seems to make it worse not lift the burden… sigh… today my head is a lot clearer though – makes everything more manageable… so I’m smiling – but thanks for the offer… I might just take you up one day! xox

              Liked by 1 person

              1. Writer McWriterson Avatar

                I understand this COMPLETELY. And definitely take me up on it. I mean it. 😘❤️

                Liked by 1 person

  4. markbialczak Avatar

    Yes, Linda, knowing you’re doing the best you can and not feeling bad about that, too, seems mighty important to me.

    Liked by 1 person

    1. The Mindful Migraine Blog Avatar

      I know – that’s what I have to keep reminding myself when I’m lying down – I’m doing the best I can! I would love a little of the energy-excess that my teenagers have though – they rarely slow down! 🤣

      Like

  5.  Avatar
    Anonymous

    This is so accurate. I live on both sides of this issue. My migraine side and my chronic pain/CRPS/arachnoiditis/arthritis/lupus side. The thing is this, I might be able to adjust my “spoons” when my chronic pain issues flare up more. There are things I can take or use to help attempt to lessen the pain. Unfortunately, with my migraines, there’s not a lot I can do once the train has left the station. I might be able to take Tylenol, drink coke or coffee, try to keep the lights/sounds low. But a migraine can essentially wipe out any spoons I have mentally allotted for the day. It’s tricky.
    I appreciated this blog. Thank you!

    Like

    1. The Mindful Migraine Blog Avatar

      Thanks for reading, and yes, some conditions allow us to juggle spoons, including “mild” migraines… but when the train has left the station, as you say, spoons fly out the window! (Sorry you have so much to contend with, know that I’m sending you gentle hugs and some good vibes!) xox

      Like

  6.  Avatar
    Anonymous

    This is so accurate. The other thing about dealing with migraines is that there’s not a lot that helps me once they start. I can try Tylenol or something if I catch the early hours in time. Maybe some Coke or coffee to amp up my caffeine.

    As I am both a spoonie and a migraine sufferer, I can tell you that I have to treat them with completely different means. Migraine stuff listed above. But my CRPS, arachnoiditis, arthritis, chronic pain stuff, I can take my breakthrough meds. I can use lidocaine cream or patches. My extra stuff might not help much, but at least I can try.

    I appreciated this one! Thank you!

    Liked by 1 person

  7. majellalaws Avatar

    Interesting. I live with neurofatigue and know about chunking and pacing but never hear of spoons of energy. Love this … 💜

    Liked by 1 person

    1. The Mindful Migraine Blog Avatar

      I think it’s mainly used by people with fibromyalgia, but it could apply to anyone with chronic fatigue. “Neurofatigue” is a new phrase for me… off to investigate – thank you for reading, and using the term – it really resonates! Linda xox

      Liked by 1 person

  8. joannerambling Avatar

    Never heard of this which makes it all the more interesting, I get most things done of a morning before my body just doesn’t feel up to doing stuff and usually after doing some housework I end up feeling exhausted

    Liked by 1 person

    1. The Mindful Migraine Blog Avatar

      I’m a morning person now, too. I go hard while the energy levels exist, then as they taper off, so do I… then it’s a slow crawl to the finish-line that is bed!

      Like

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