Monday, 2 December 2019

#SeasonalSonnets 2019: 2nd December

Hello my lovely readers

With gratitude for the kind responses to yesterday's entry, today's continues the theme of the past emerging in (and merging into) the present. It is about one of the people, beyond my immediate family, who was crucial to my childhood development and remains important now - my godmother Jenny.

We are staying with her in Cape Town, to where we've just returned after a long drive from McGregor. So I apologise (both to her and to you) if this isn't my finest example of a poem. But I didn't want to miss a day so soon into this series; nor a chance to cherish this awesome feminist activist who is so kindly opening up her home for the majority of our time in South Africa. Below the poem is a selfie she took of us in the sunshine outside Pony Cottage, where we stayed this weekend.

2nd December 2019

Today I write an ode to my dear Jenny
who has, since my young years, been an example.
It's nigh impossible to list how many
things she has taught me - and yet the number's ample.
I learnt from her to love Joan Armatrading
and how to navigate the world online.
She showed me ways to begin arbitrating
between opinions and start forming mine.
She even offers space for us to argue,
by teasing out exactly what we mean,
and (though, sometimes, we might find it quite hard to!)
a kindred spirit she has always been.
For, above all, we share a sense of humour
and her laugh's cheekier than any rumour.


Sunday, 1 December 2019

#SeasonalSonnets 2019: 1st December

Hello my lovely readers

Now that it is the start of December, we're also at the beginning of this year's Seasonal Sonnets series, which is in turn the first part of the project I have planned - to write a poem for the next 365 days.

This opening entry, and indeed this year's entire series, might be perceived by some as decidedly unseasonable. I'm writing it from South Africa, where it's summer. However, as I spent my earliest childhood over here, to me it seems exactly the right way around. That sentiment is the substance of this sonnet, since we're staying with old friends in the mountainous Western Cape village of McGregor. Last night we went to a gig by yet more old friends, the awesome Edi Niederlander Trio, and today we're just chilling in nature (in the shade). Below the poem is a picture of the surrounding countryside.

1st December 2019

This year's a homage to much younger me,
who finds relief and safety in warm weather
and really thinks festivity should be
in summer, like Christmases she remembers.
I'm thrilled now we have made it home at last
and grateful that my body lets me travel.
Revisiting some places from my past
is helping me catch threads which have unravelled.
Shy hopes are building for my future too,
inspired by the chance to be in nature
which is at once familiar and new -
I feel that 'young me' may now mature.
For scenes to mark the start of this December,
I'm glad to have the beauty of McGregor.



Thursday, 21 November 2019

Children's Grief Awareness Day 2019

Hello my lovely readers

This post is perhaps earlier than expected. It is neither December, nor the start of my Seasonal Sonnets series, and it isn't the beginning of my poem a day project.

It is, however, a poem. Today is the global Children's Grief Awareness Day, and the end of Children's Grief Awareness Week in the UK. The theme this year is 'Lost for words'. That struck a chord with me. Not only did I find it difficult to talk about my grief growing up, but I used poetry as a private and more abstract outlet. And those of you who have been reading this blog a while might remember how scared I was when that coping mechanism, which I've used since I was very young, seemed to disappear entirely in the summer of 2017. Along with all other creative writing forms.

But, thanks to a combination of factors, from therapy sessions to the support of the bereavement buddies I've met through groups like Let's Talk About Loss and The Grief Network, my young adult self is finally getting brave enough to process my experiences properly. And, with that talking, my writing seems to have reappeared as well. So I wrote this poem last week, in honour of my child selves, and in solidarity with kids who are going through grief. I'm rather terrified about posting, but if it helps one other child (or adult), then it's worth it. Please know you aren't alone, and your feelings are okay and allowed.

Here, shared with love, is my perspective:


This is a note for little me
in plural; who wrote poetry,
at ten, eleven, twelve, fourteen,
and all the ages after then.

We wrote to cope in 2001
when Gemma, first, was suddenly gone
and kept it up throughout our teens
‘til five in a year made seventeen.

It was easier to write than talk
for otherwise our brains would baulk
and shout the screams inside our heads
when yet another friend was dead.

But, with five almost at once,
we could not find the write response
nor could we find the words to say
and so our minds were shut away.

I felt lost for what to do
but now I know that’s okay too.
Sometimes words just won’t describe
the feelings that we hold inside.

And sometimes, though aged twenty-seven,
we need rhymes that sound like we’re eleven
or younger even, perhaps ten,
since that’s the age we ‘lost’ dear Gem.

And that’s the age I revert to,
when there’s the news of someone new,
transported, body, mind and soul;
fresh grief reminds me I’m not whole.

And then I’m sliced in two once more
as teenage me lets out a roar;
an ever present adolescent,
lip wobbling after younger precedent.

These foundations were what built my twenties
as the numbers grew aplenty
and piled up the paradox
that, needing them, my words were lost.

My mind became not one but many:
I had no proper hold on any.

But, though I have felt split apart,
my nearly thirty-year-old heart
is learning to connect the halves
that make up all my little selves.

Voicing, together, that we grieve,
we’re finding some mutual relief.
Tasks of talking through our pain
have sparked our writing up again.

Though I still reel from the hurt,
I’m glad to put it into words.

Sunday, 6 October 2019

World Cerebral Palsy Day 2019

Hello my lovely readers

So, I've submitted my PhD, and had planned to be writing a poem a day from the beginning of this month. That hasn't happened yet...because I didn't bank on quite how exhausted I'd be. Not just intellectually but physically. I've therefore decided to postpone the start of the poetry project until December. I'll be writing Seasonal Sonnets then, anyway; albeit from a summery South Africa.

I would usually be sad about the delay - but this post is to convey the opposite emotion. Because today is World Cerebral Palsy Day. And, if there's one fundamental thing I learnt through all parts of my PhD process, it's that the effects of CP are often surprising. This is true even of my still-upcoming viva (where I have to defend my thesis), because that kind of oral exam is in some ways more accessible to me than six hours sitting beside a scribe. Although public speaking as myself remains terrifying, the energy required to have what is essentially an academic conversation is less than I personally need to maintain focus in a more traditional exam environment.

And that's the point of this post. For me, CP nominally and most obviously results in physical impairments like muscle spasms - but it also affects my sensory processing abilities, my energy, and my sense of self as I exist in the world. Literally. Sometimes it feels as though parts of my body have disappeared.

Whilst I was finishing off my thesis, the level of focus required meant that I locked away some of those other symptoms, causing them to manifest more in tightness of muscles and ligaments than fog or processing issues. Now it's done, I've regained some of the relaxation I've been aiming to maintain over the last few years - but the fog and difficulty with processing has seeped back. Because I'm tired.

But I'm proud, too. I PhDid it. And now I need some time to recuperate before embarking on another project which is similarly ambitious in both scope and length. But that's okay. It's life alongside CP. Without which I wouldn't have written my particular PhD, nor probably have developed such a love of poetry.

So, on that note, happy World CP Day, and love and spoons until December.

Jx



Wednesday, 7 August 2019

#WordyandWheelyWednesdays: Wheeling to the end (of study)

Hello my lovely readers

That plural 'readers' feels a bit presumptuous following such a long break from writing posts, but some habits are nice. Anyway, this won't take (that) long to read. It's just to say I'm back, because I've got a fortnight off before I get feedback on a thesis draft. Then I'll be back to regular posting fairly soon, too, after many, many months away. I submit my final thesis at the end of September, and my first plan once it's in (as a treat after four years of mostly academic writing) is a project where I write a poem each day for a year. Some short, some longer. Thirty-one of which will be sonnets, as part of the Seasonal Sonnets series I've had very varied success in keeping up with throughout December over the last two years. Some of the others might even be haiku, because I've fallen in love with that shorter form and the burst of disciplined creativity it offers since I've had to snatch moments between paragraphs of my PhD.

Either way, in order to have a place to put them, and to keep myself accountable about actually writing, I'm going to post the poems here. Possibly daily, possibly weekly - maybe as part of Wordy and Wheely Wednesdays. Who knows!? Much like the poems themselves, the structure of documenting the project is pretty nebulous. It has to be, until October, but I want to get excited about writing creatively again and poetry - my first, and favourite, form - seems a good place to start.

So if you'd like to read, it'd be great to have you along for the ride. (It wouldn't be a Wordy and Wheely post without some disability puns, would it, eh?)

Love and spoons 'til then.

Jx

Saturday, 6 October 2018

World Cerebral Palsy Day 2018

Hello my lovely readers

It's been a while, as you'll note from the change in font. (That happened some time ago, too, for accessibility purposes - but I had no energy to write a post then.) Contrary to my usual practice, though, I'm not going to apologise for that; because I took a break for self-care, and self-care is important. So much so that that's the subject of this returning post, which I'm writing for World Cerebral Palsy Day 2018. I have a historical habit of reappearing on this blog for World CP Day, but that feels apt, because I live with CP. So a day centred on awareness of it seems both suitable and sensible to document here.

Not least due to the fact that the majority of the time during my break from blogging has been taken up (alongside my PhD) with navigating my way through new understandings of what life with this condition means. The first year I wrote about today, I focussed on the things I've learnt from CP - I suppose, then, that this year's post deals with things I've learnt about CP. And, as a bridge between them, there is (helpfully) last year's post. In it, I set out some things I wanted to explore and hopefully achieve with my CP (all of which were from my 'Thirty Things Before Thirty' list). Because, reading back over that list this morning, I realised I've met each of the goals I wanted to in the last year, never mind before thirty; perhaps not in the way I might have expected, but things often happen like that.

They were: sit in a manual chair again, fly again, have one professional acting credit, and 'be emotionally and physically ready' for a relationship. 

I won't go into detail about each of them, because that's not the point of this post - but I draw attention to them in order to make that point.

For various reasons, and through help from a variety of sources, I've learnt in the year since the last World CP Day that it means I do things differently. That might seem obvious and, on one level, it always has been. I've always understood it. But I know now that that understanding was superficial, about practical things like needing help with dressing. What I didn't fully comprehend was the more nuanced ways in which my neurology impacted my engagement with the world - that, because CP results from a brain injury, I need to understand my brain if I want to make a difference to how I live in my body, both physically and emotionally.

Again, something I already knew in theory. I've probably even written about it on this blog before; but, when you spend a lot of time doing academic things and are visibly disabled, the refrain tends to be 'well, there's nothing wrong with your brain'. So reminding myself that I'm allowed to take time to work on that brain, and that that is necessary for my success rather than a sign of failure, can take some doing. Especially in the current climate of constant movement and productivity.

But it's working - and it's worth it - so I'm so glad I've been brave enough to give myself that space. It's helping me to be more at peace with my CP, along with many other things.

I hope you're all okay with me doing that, and I hope, too, that you are able to take similar space in the areas you need to do to be healthy (within the parameters of what that means for you). I haven't left this blog completely, and it means a lot that you're still reading.

Love and spoons until next time, and happy World CP Day!

Jx
 

Monday, 23 April 2018

Solace via Shakespeare in Gratitude for My Grandi

Hello my lovely readers

It's been a while (and it's likely to be a while again after this post) but I'm back briefly, having worked hard to find my words. And it feels apt that I'm back today, for two reasons. My last entry, on the last day of last year, was about being back in Canada to visit with my Grandi and Gramma and written, in large part, in gratitude for all the things I associate with both the country and them. This post finds me once again on the other side of the Atlantic, where this weekend we gathered as a family from across the globe to honour the memory of that wonderful man, father and grandfather.

So a sad but significant coincidence, and one which makes me smile. Not least because my contribution to the celebration of his life was a sonnet, and that leads to a further coincidence. Today is the first day I've felt confident enough to write this blog post - and it also happens to be Shakespeare's birthday. I guess it's apt, then, that I may combine in it a homage to two of my great loves, who have both taught me much I treasure. I'm grateful to the bard for giving me the structure (by way of Petrarch) in which I so often seek solace when struggling, and I'm forever grateful to my Grandi for so much of the wisdom which makes up my life's philosophy.

I'm not quite up to my usual standards again yet, so I'll sign off now, and leave poetry to plug the gaps of my prose. Here is my sonnet - a fusion of my three familial cultures (written in the style of a British playwright, about a man from South Africa who lived in Swaziland, and spoken in Canada) that pairs the old with the new and finds gratitude amidst grief:

This sonnet is an ode to dearest Grandi,
who guided my life from its youngest years

to adulthood (with whisky or a brandy)*

and held me when I laughed, or cried hot tears.

But what I feel most, now, is huge thanks,

for all the wondrous moments that we spent

that I may store, secured, in Memory’s banks;

a testament to just how much you meant.

I’m sorry that you never got to ride

your wish in later life (a chair like mine!)

but please know, as I zoom, you’re in my mind;

I promise to ‘keep smiling’, rain or shine.

I’m so sad I must tell you ‘hamba kahle’** –

I’ll try and live the lessons that you taught me.

*He was responsible for my love of
**Zulu for 'go well' - an affectionate goodbye