Capability vs Capacity

Thanks to some excellent advice from a good friend I’ve been thinking about the difference between capability and capacity.

Knowing the difference helps me to choose what I can take on and what I have to politely decline.

It’s really hard to see yourself as no longer capable when Fibromyalgia puts the brakes on your life.

If you’re like me and you’ve always been capable or high achieving at work, or in any role which is outcome driven,  this will be tough.
If you’ve always been ‘everything to everybody’,  this will be tough.
If you have achieved things that you are proud of, but can no longer do,  this will be tough.

It’s especially hard if your identity has been tied up in those capabilities or achievements.

I was incredibly career driven – a teacher for over 30 years, I’d written exams, curriculum standards, advised teachers in my subject area and taught new teachers their craft. The very definition of capable! Letting all that go was tough & I’ve had to re-learn what is important to me.

Turns out what’s important isn’t my achievements, it’s the things I value the most – connection, family, creativity, helping others – and having the capacity to do those things is vital. I’m taking more quiet time (hello jigsaws puzzles) between ‘doing’ to just ‘be’.

Capacity is changeable and fluid

I always assess how I’m feeling before I decide whether I can do something. When assessing my capacity I work out how taxing whatever I’m asking of myself will be, physically, emotionally and mentally. I also think about how doing it might affect me down the track.

AND I always remind myself that my capabilities have not changed – I’m just choosing to apply my skills in different ways, or saying, no thank-you, when it needs to be said.

If what you’ve read today resonates with you & you are wondering about what working with a Fibromyalgia coach would be like, we can meet for a chat. I’d love to explain how I can support you! You can book in for a chat here. 

Keep the holiday feeling

What a holiday we’ve had..

Despite Fibromyalgia hitching a ride

It’s summer here and we’ve been lucky enough to travel round the South Island of New Zealand in our van. If you don’t know this part of the world then I highly recommend Googling some images. It’s phenomenally gorgeous (no bias at all!!) This holiday has been a while in the making – we needed to plan for it to be a success with some extra travellers on board – Fibromyalgia and chronic pain.

The van isn’t fancy, but the bed is super comfy (a non-negotiable requirement for my Fibro body) and we really enjoyed living a simpler life for a few weeks, with our only agenda being to see amazing places, walk when we could, & chill out!

And I felt great! And by great I mean my cup was stuffed full to overflowing with great experiences I could turn to when I was in pain after a big day (inevitable – but worth it!) and (crucially) after life kicked in when we returned.

I’m back at work now and I need that holiday feeling more than ever.

On my return home I found myself thinking – how can I keep this feeling? – relaxed, carefree, able to handle the days when I’m in pain or the stresses of life weigh heavy on me.

It occurs to me that what happens on holiday – especially one like ours which was so visually mind blowing – is that life grows bigger – even if the pain does not get smaller. Bear with me..

I have some great images to replay in my head for when I need them.

Maruia Hot Mineral Springs

I can recreate that holiday feeling in my imagination WHENEVER I LIKE!  Looking out of the van from my bed, relaxing in a soothing mineral pool, the beauty and wildlife that surrounded us – I have lots to draw on now. And thanks to my daughter getting us a digital photo frame for Xmas I see my photos every single day and remember the feeling that I had when I was there.

Keep the holiday feeling

The key to our holiday success was less! It was a simpler life for the weeks we were away with less stress and less things to do. We weren’t rushing and had very few deadlines. I slept for longer and soundly, and read 4 books!

The optimal word here is LESS – and that’s the holiday feeling I’m trying to keep.

Simplifying life. Checking in every day to make sure I’m not overdoing it and that I’ve put some joy in my day to make sure that LIFE is bigger than PAIN. We can’t always ditch our responsibilities but we can make choices about what is most important to us to do and not do.

So, if you are to take one thing away from my experience I’d like it to be this

Even if you are not able to have a holiday right now or any time soon – I’d like you to close your eyes and imagine a place you have loved, that has made you feel relaxed, at peace – somewhere you can return to in your mind when times are tough.

You don’t need to strive all the time

Doing less of the ‘shoulds’ and a little more of what makes you feel good is a great place to start.

I’m here for you. Take care!

Deb

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