Breathe in: breathe out

I had said to myself I wasn’t going to write this week. As of two days ago, I went on strike.

I wasn’t sure if it was my body or my emotions that were the part I had overdone but either way, I felt like an elastic band that had snapped, and was wandering through life in a bit of a stupor. (I’m lying, by my use of the past tense. I am still in a stupor). I told myself I would give myself permission not to do my Story 101 writing course assignment about the rhythm of creativity – because I am wrung out and have no more ideas, no more words, nothing left of myself to give to anyone.

And then the words just snuck in through the back door of my mind, and here I am, writing.

****

I should probably tell you a secret: I am writing a book. (I am trying to write a book).

It seems that every time I write a post about how it feels to have M.E., thinking that it is self-indulgent and no-one will want to read it – it goes huge and people thank me for saying how it really is. I had so many ideas for blog posts about M.E. and what it really feels like, I realised it was long enough for a book. So I started writing it, secretly, with my spare energy, spare minutes. I am hoping to publish it in January 2014, via Kindle. (I have a few other writing plans up my sleeves after this project, but this is the first.)

It feels foolish and exciting to write these words, to confess my ambition whilst realising I may never complete it, and I say it to you whilst shuffling my feet and looking down at the floor. But I’m telling you anyway, because I am realising that to do anything in this life I need deadlines, accountability – and cheerleaders.

Though my mobility is still pretty terrible, my cognitive energy has been good and steady for a few months, so I have been able to write more, and I feel excited and energised by it all. And then there are weeks like this week, where I feel listless and wordless and wondering what on earth I am doing; I am in a slump, with no idea how I can flick myself out of it.

*****

The word ‘slump’ makes me think of my boy.

I love the transparency of toddlers. Some people complain about the phase: the tantrums, the embarrassing things said to strangers – but I like the honesty of it all. They sigh, and you know it is time to change it up.

Yesterday, we were building Lego houses, and we were completely absorbed in the fun of deciding where to put the fifth bed – and I heard it: the sigh. The slump. It was subtle, but it was there. The completer-finisher in me wanted to carry on but my Mummy radar knew this was the time to stop.

We are not designed to do the same thing for a long period of time. We breathe in – we breathe out – even our anatomy is in a perpetual state of flux. My boy had reached the end of breathing in, sitting down – he needed some OUT; he had had enough quiet and he needed some noise. Toddlers are no different to adults: we just hide the sigh a little better.

“Would you like to go and run around outside?” I asked. His eyes brightened and we put on his wellies, and I sat and watched him run in circles in the garden, whooping, laughing, shouting; his breath releasing the energy and emotions that were stored up from playing.

*****

We are not designed to be continual contemplatives, most of us. Nor are we designed to be constantly running a marathon. We need to pray, to think, to dream, to inhale deeply of God’s word, and worship in the quietness of our hearts; and then we need to breathe out – to run, to serve others, to discuss, to walk alongside, to work, to produce.

We inhale: we exhale. If we exhale for too long we find ourselves gasping for air; if we hold our breath for too long, we burst. Sometimes we need to listen for that sigh, the slump. I had heard it in my soul.

I saw it in my boy, his slower pace as he clomped around the garden, the restless way he was fiddling with the stones.
“Shall we go in now?” I said.
“No! I LIKE it here,” he said, but his tone was whiney and I knew we were about five minutes away from him losing concentration, falling over and crying. We went inside and cuddled up on the sofa together, and we both took a big breath as we started to read The Wizard of Oz.

****

My health means I have the lung capacity of an 80-year-old (almost literally, and very definitely metaphorically). I have been breathing out for too long, just in the bursts of writing and the enjoyment of chatting with friends. I have loved it; I have been whooping and hollering and laughing, but I have also been overwhelmed and I am five minutes away from falling on my face.
I have heard the sigh. I need to pause.
This is what I will do: I will not write any more today; I will read. I will read the word of God and breathe in his life-giving Spirit, his holy Breath.
Over to you:

  • How do the rhythms of breathing in, breathing out; creating, receiving; working, resting ebb and flow in your life?
  • Are you feeling the need to ‘breathe in’ or ‘breathe out’?

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58 Responses to Breathe in: breathe out

  1. HopefulLeigh 10th May, 2013 at 10:46 pm #

    I’m so excited for you, Tanya! Whatever I can to help, to encourage, just say the word.

  2. Kath 30th April, 2013 at 12:48 pm #

    I like the flow here, Tanya. The inhale and exhale is so true. Keep breathing, and writing. It’s a blessing.

    • Tanya 3rd May, 2013 at 1:40 pm #

      Thank you, Kath!

  3. John Boyett 29th April, 2013 at 7:10 pm #

    Thank you for all you say and write. I was introduced to yuour writing by my niece, Micah Boyett.
    You have helped our family immensely. My wife ,Donna, has undiagnosed M.E. I say that because all the specialists, general practicioners, neurologists, etc. we have ween over the last 10 years have not been able to put a name to her condition. Even after first finding you and seeing the first mention of M.E. ever. We knew that was causing her suffering. But when we discuss it with her Doctors, we get a blank stare back. Even when I list symtoms of M.E. and how they match her symptoms they don’t seem to care or recognize that this might just put a name to how she suffers.

    We just pray and thank God for discovering you and putting you in our path.

    • Tanya 3rd May, 2013 at 1:36 pm #

      Wow!
      First – I LOVE Micha and her writing – and I’m so glad you found me through her.
      Second – oh boy- I am just feeling for you and your wife. It is so frustrating going back and forth to the doctor with them just telling you endlessly what it ‘isn’t’ instead of what it is, the shrugs, the ‘normal’ tests… I am so sorry that you have been treated so poorly by doctors.

      There are a few good ones out there, but M.E. is a tricky illness to have – some doctors don’t acknowledge its existence, and some just don’t know what to do with it. My blogging friend Jocelyn of No Poster Girl sees Dr Cheney, who is well-regarded in the M.E. community, as is Dr Byron Hyde in Canada. I hope that some of the links on my site will be of help to you as you discover more about the illness.

      Sending you both SO much love and prayers.

  4. Chrissie B 28th April, 2013 at 6:39 pm #

    Hi Tanya

    Having prayed for you and your family, on and off, over the years (your marriage, time working for IFES, and more recently with ME), I’ve been directed to your blog by your parents-in-law. I find that I, too, now have cfs/ME. It’s been great reading the small bit I have managed to read today. Thank you for it – for your honesty, insight, and encouragement. Will read more soon ????. Would love to hear from you when you have the time and energy…… Sorry I can’t concentrate again…… God’s obviously using you in your illness, and may you know His many blessings in it too.
    Love and thanks
    Chrissie x

    • Tanya 3rd May, 2013 at 1:27 pm #

      Oh Chrissie – I am SO sorry to hear that you have CFS/ME. Thank you for using some of that precious brain-energy to write this note. I am praying for you – praying for you in the scariness and fear of it all. Sending you much love. Xx

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