Downright Joy

Discovering joy in unexpected places – a journey into Down's syndrome, Dyspraxia & Autism


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Trampling Through Tulips

Photo by Marija Zaric on Unsplash

For those of us well versed in all things Down’s syndrome related, we are likely very familiar with the poem ‘Welcome to Holland’ (You can read about it here if you’ve not come across it). 

Perhaps it was handed to us as new parents around the birth of our baby; a child born carrying an additional chromosome.  Or perhaps we stumbled across it as we trawled the internet searching for answers to allay new found fears and uncertainties in those early days of parenthood.

It’s a poem that divides opinion in our community, but this isn’t a post about its virtues or its vices. If anything, I’m Team Italy…mostly because of my family connections with a country that has long had my heart for many decades. So, Welcome to Holland did little for me when I was introduced to it some 14 years ago, but it still has its place for others, I cannot deny.

In reality, neither my experiences of the Italian way of life, or my understanding of how the Dutch operate bear much resemblance to where and how I actually live, as the parent of a teen with Down’s syndrome and complex needs.

Mamma Mia! 
The tulips round my way are long past their best.

No. Instead, I find myself residing here, in Suburbia, living at Wit’s End. Brought here on the Sleepless Night (after night) Bus, without it seems, a return ticket. Hopping on and off along the way to search for answers to this month’s health dilemmas. No, I’m wrong…..searching first for an appointment to look for answers to this month’s health dilemmas. Trying doors that say “Welcome” or “Open” only to find them cruelly locked from inside. I think, on occasion, I may have imagined the sound of laughter from within. 

And so here I am, living at Wit’s End. Carrying little else but the complex needs of my disabled child. Bags still hopefully packed with my dreams for her life. For our lives. 

Yet it’s here, not in Holland or Italy, that I find, in fact, I’m not alone. If I thought the centuries old, cobbled back alleyways of my beloved Sorrento were crowded with fellow travellers, it’s nothing to this place. It’s not very Instagrammable though, this Wit’s End. I’ll give you that.

But it’s here we gather. Each bringing our own stories of how we got here, of who would not listen to us, of who dismissed our fears or rubbished our requests for help. Telling each other stories of how many times our loved ones (and us as care givers) were failed, ignored, mistreated, maligned.

You would be forgiven for thinking that Wit’s End is the most depressing place on earth. 

And yet it is here I find my community. I find those who reached this destination long before I did, and are ready to welcome me into their homes, to explore their hive-minds, share their lives filled empathy, understanding, compassion, humour and so much more. Here I find, almost without fail, someone who will ask me “Have you thought about this…?” Or “What about trying this, it worked for us.”

It’s here, in the village of Wit’s End, I’ve found people who want to know and understand my child, and me. I’ve found Complex Carer Nurses, I’ve found parents of children with Down’s syndrome and or other conditions and complex needs. I’ve found other Wit’s Enders ready to make me laugh and not take myself so seriously. Quick to bring perspective, a joke, a slice of cake and a cup of coffee. There is, I’ve found, an end- less supply of Wit to be found here and I am eternally thankful for it. Heck, in my neck of the woods there is even our own Farm …a place with those ready to share our load and give us respite from our travels!

One of the most beautiful things I found about the Italian way of life, aside from the art, the architecture, the scenery, the beautiful weather, the food…..I could go on……is how much they know each other and are known by each other.  The sense of community there, I’ve always felt, is to be envied by us more insular Brits. But perhaps my beloved Italian culture is closer to my own experiences than I think.

Being known and heard is everything when you are a carer to a child (young or old) with complex needs and disabilities.  I may have been driven on many occasions to Wit’s End by circumstances and by not being seen or known. Yet when each time I arrive, without fail, I find friendship, laughter, hope and comfort that I am not alone.

Welcome.


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Blessing

Photo by Ross Sokolovski on Unsplash

Burden is a beautiful, all-consuming word.
She is a gift, costly to many, priceless to me.
Too heavy, too expensive for some to receive, carry, care for,
Love, nurture and enjoy.

Burden is a noun as well as a verb.
A load to be shared, a weight best carried when spread
Across the shoulders of an entire community,
Not one person or two or even three.

Burden can be known by her alter egos,
Significance, Substance, Intention or Meaning.
Known also as Cargo, she can be most cumbersome!
Gold, real gold, weighs its worth so heavily.

Burden carries with her the full range of human emotions.
Which weighs more; a tonne of feathers or a tonne of bricks?
Feathers make for the softest of pillows for weary heads
Bricks build on each other, mortared together to surround, shelter and support.

Burden is a beautiful, all-consuming word.
And I am refined by her syllables.
Thrilled when others come alongside to share in her Meaning,
They add more bricks along the way, building all our belongings.

Burden (whose real name is Blessing)
Has just sat down on my lap, smiling, to watch heavy rain lash against our window.
Forgive me, but I’ll just have to put this down for a while and finish it later….❤️

“I sometimes hear old people, including Christian people who should know better, say, ‘I don’t want to be a burden to anyone else. I’m happy to carry on living so long as I can look after myself, but as soon as I become a burden I would rather die.’ But this is wrong. We are all designed to be a burden to others. You are designed to be a burden to me and I am designed to be a burden to you. And the life of the family, including the life of the local church family, should be one of ‘mutual burdensomeness.’ ‘Carry each other’s burdens, and in this way you will fulfill the law of Christ’ (Galatians 6:2).John Stott The Radical Disciple


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Silent Disco

Photo by Bozhin Karaivanov on Unsplash

Who saw you today?

Not on the pages of an inclusive advert, or some clever marketing campaign.
Profits helped along by an investment of virtue signalling.
The ahhh factor leaves a sense of pride, of doing good.
Progress none the less, positive images welcomed by most, including me.
No criticism, no envy, there’s room for us all, and all of us are needed, ultimately.

Not on the pages of social media, as we scroll, pause and smile for a few brief moments to notice difference and give it a like.
Nor in the sound bites and platitudes of an inspirational news story or televised fundraising event.
Down’s syndrome mentioned to the masses in the same breath as your name.
As if your difference it isn’t obvious from your photo and therefore necessary to firmly and quickly affix.

In a digital age it seems to me that these are the places you are most definitely wanted.
Needed even.
Increasingly so.
I’ve wanted this too, and many I know who work tirelessly hard to bring this about, for reasons of good.
Yet, the varying motivations for wanting or needing this exposure seem, at times, to compete, and end up blocking you entirely from view.

Were you routinely seen today in the park, or the mainstream school or the cafes, restaurants or bars?
Or in the Church or the shopping centre, or the swimming pool?
How about the Pharmacy, or the Dentist’s waiting room, or when queuing for a bus?
Will you one day be seen at the Jobs fair, or the college open day; are these places even open to you?
Your kind of diversity seems to do best in a photo opportunity; contained within (Facebook) borders that have yet to be crossed into a new way of life that is good for us all.

Did anyone, aside from your teacher, see your Monday morning joy-face as you entered the classroom of your Special School today?
Or hear your laughter at the same point in the same song we sing together every day?
Did anyone see you fall silent last summer when your world shrank a little more and, for a few months, you rarely left the house?
Did they get to share in your delight as you danced in the living room for the hundredth time to Daydream Believer?
You danced like no one was watching: you’d do the same even if they were – a silent disco isn’t the place for you.

Are you needed by society? Definitely.
Are you wanted by society? Yes, but only to a degree.
I’ve noticed you are routinely missing from it, yet, it appears, you are not routinely missed.
Except by those precious humans in our lives who hear for themselves the music you play and collect the colours you bring; they make sure that you are never unseen.
And, except by me.

For the “foolish” things of God have proven to be wiser than human wisdom. And the “feeble” things of God have proven to be far more powerful than any human ability.

(1 Corinthians 1 v 25 The Passion Translation)


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The Nurturer

Image by Krzysztof Mandrysz from Pixabay

We asked for help, a year ago.
It was hard to do.
Pride got in the way, many times; weariness stood over us, blocking our view
Of what help could mean, not just to us
But more importantly, to you.

Years of thinking we should be able to cope
Manage by ourselves, not admit any hint of defeat.
It felt wrong, somehow, to ask just for us
But we should not have been afraid to ask
For you.

Help emerges, stepping very gently in on our daily scenes.
Those tasked with listening, listened.
Compassion now walks faithfully, routinely, through our front door.
She rolls up her NHS sleeves, and as I back slowly away, out of sight, I glimpse her smiling, so very tenderly, at you.

We never knew, incredibly, we never knew!
That help intended for us meant new independence,
A new face, a new friend, a giver,
Someone new, as well as and other than us to smile with, nurture and care

For you.

“You can buy two sparrows for only a copper coin, yet not even one sparrow falls from its nest without the knowledge of your Father. Aren’t you worth much more to God than many sparrows?” (Matthew 10 v 29 The Passion Translation)


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Pocketful

Photo by Alexander Grey on Unsplash

We collected five on our way home from the hospital today.
Five!
Not two or three or four, (which would still be good) but five.
In February of all months, or Kale-monath in Old English, named after a cabbage, I have gleefully learnt.
A perfectly sensible name for this month, at least it is if you happen to live in England.

Five; all now safely stowed away in my coat pocket.
Snatched almost rudely, as if in short supply then shoved deep inside lest they be stolen away.
Now stashed amongst scrunched up tissues and the remnants of an autumn leaf I have not had the heart to throw away, both constant reminders of the season we’re in.
A pocketful of things I would not be without, when I am with her.
Free stuff.

Five in one walk is a record for us.
Our faces lowered as we battle the elements of a dark, bitter afternoon; February revels in its cruciferous status.
She laughs as her wheelchair jolts and bounces over once subterranean but now emerging tree roots.
I do not laugh; today I am weary of visiting hospitals and sitting through endless appointments, either in clinics or at home for this won’t take long and they’ll be as quick as they can.
I am cold and wet and her wheelchair is heavy and these roots are monstrous and, and…oh hello there…thank you, yes you too.

Our pockets are filled.
Hers with the joy of the journey home, the wind and the rain are her elements, mine bursting with the lightest of finds.
Five genuine smiles given to her by five strangers, as they hurried by on this dreariest of winter days, handing out free stuff worth ten times its weight in gold.
Five of the kindest, ordinary faces giving a moment to honour her, not to pity her (we don’t collect those), recognising then marvelling at the treasure she always carries.
And reminding me, all over again, of the utter privilege that is every day caring for her.

A twinkle in the eye means joy in the heart, and good news makes you feel as fit as a fiddle….

Proverbs 15 verse 30, The Message


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The Giver

Photo by James Coleman on Unsplash

I saw Sadness leave one day back in early September,
It stood up and walked out through the door.
Without a word of warning, it simply left your face.
Not pausing to say goodbye or farewell
But still, leaving me shocked to the core.

I did not notice when Sadness came into your life,
This was not someone I thought you of all people knew.
Yet the moment Sadness left you was also the moment I saw
That for many days, weeks, months even years more than I’d realised
Life had been growing harder for you.

Sadness moved in on you, on us, so very slowly, stealthily.
A Master of Disguise in lives lived permanently on high alert
For the next medical emergency or serious health concern.
Sadness was, at first, just a virus then perhaps it was not…but if not, then what?
Doctors looked for a reason why you were no longer yourself; why so inert?

The day Sadness left was the day I knew it had ever even stayed.
That soft autumnal morning as I signed to you ‘the first day of school.’
After months of your outside world shrinking in ways that had broken my heart
Your face looked up and THAT smile at once returned, revealing the truth
You’d been sad for too long, not ill.

Christmas came in September, with gifts of friendship,
Farm visits, fun and laughter at school, at home.
Connections once again made with others who bring you joy.
Inertia left with Sadness, scooping up Entitlement who I confess I’d invited to stay.
Leaving room once more, at this particular Inn, for those who make their love for you known.

I’m thankful, this Christmas, for the Giver as much as I am for the Gift.

Happy Christmas to all who celebrate with us x

The thief comes only to steal and kill and destroy; I have come that they may have life, and have it to the full.

Words of Jesus, recorded in John 10 v 10, The Bible and my prayer for all who read this.


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Lifted

Image by Bianca from Pixabay

Some people yearn for a glimpse of the sea.… its shimmering expanse opening up as they travel along a coastal road on a summer’s day. They taste it long before they touch it. The sight of the sea can thrill or calm, excite or pacify, threaten or invite. Such is its pull; drawing a person closer one moment, sending them running backwards another. At times, its power is too alarming and we retreat behind its defences where we are forced to watch and wait for calmer days. For all its drama, rarely does anyone tire of the sea or wish they had not experienced it. 

I yearn more for a lake than I do the sea. Drawn by the instantaneous peace I experience when nearing the gently contoured edges. I am calmed by the stillness of the water, occasionally disturbed by a surfacing carp or foraging moorhen. Dragonflies dancing across its surface, quickstepping back and forth, their tiny wings catching hold of the early morning sunlight. Today, I am captivated not by dragonflies but by an altogether more solitary beast. I am sat on a wooden bench in the shadows of the surrounding trees that bow in reverence towards this small fishing lake. Here, I find myself restored; not by peace, but by struggle.

A Heron, who naturally lays greater claim on this lake than I do, has patiently been standing sentry, some thirty metres away from me, for what feels like an eternity. A backdrop of biblical bulrushes and reeds afford it some cover as it waits. And waits.

I urge Heron to get on with it and be off with its meal so I can read my book. I came here early, before anyone else was up. It’s my only opportunity of the day to read without interruption, but I cannot take my eyes off this lone fisherman. The book remains unopened in my lap.

Heron takes no notice of my whispered exhortations and never once drops its guard. Breakfast; the most important meal of the day around these parts, remains its resolve. Finally, Heron’s patience is rewarded and breakfast is served. Heron darts forward with speed and precision. Denying its own smoky-grey awkward frame, Heron emphatically takes its prize.

Heron’s prize, a small Carp, has other ideas, and is in no mood to be on today’s menu at the Lakeside Brasserie. Carp contorts and twists violently, fighting for its life and putting up an immense struggle of its own.  So much so, I’m conflicted by who I want to triumph. In this magnificently terrifying moment, both need the win, though skipping breakfast is ultimately preferable to losing one’s life. Heron may disagree and assert that these things are not mutually exclusive. Heron has no need to explain this to me of course. Heron needs only to win.

After an age that in reality lasted seconds, Carp seizes victory from the jaws of defeat and leaps free of Heron. Miraculously, Carp lives to swim another day. Heron appears somewhat off its game, a little weary, perhaps. I’m definitely with Heron now. Moments later, Heron takes flight. Defeated, yet never looking back at what might have been. Leaving only a few ripples in the lake behind it; fading evidence that there had ever been a struggle at all.

I am in awe that such harshness exists alongside such beauty. And I am especially in awe of how Heron deals so graciously with this disappointment and loss.

For our family, it’s been a summer marked by disappointment and loss. Downright joy has, at times, caved in to downright fed-up or even downright sad. The unexpected death and loss of a cherished family member, as well as other un-foreseen losses and discouragements along the way has meant that this summer has felt particularly harsh.

It has become all too easy in the midst of troubles to lose sight of the good and the glorious this summer; the kindnesses of others, a brilliant family wedding, this precious holiday, a trip to the circus, coffee and cake with friends, music, laughter……

And, as always, the grief and frustrations have related to events that my daughter, Hazel, who has Down’s syndrome and Autism, simply does not and will likely never understand.

The troubles of this world, for the most part, do not trouble her.

And this is, unquestionably, her gift to us.

Her laughter will often erupt at the most inopportune moment, leaving melancholy no choice but to scoot over and make room for joy.

Her joy.

Her joy becomes our joy.

Her care free heart is free to care and it cares, so often, for us.

Struggles are real, loss can be deeply painful and disappointment may crush, but joy is still to be found and welcomed alongside them all. My favourite poet, Mary Oliver, wrote about this juxtaposition in ‘Heavy’, her extraordinary poem on grief. If you love poetry or are grieving for someone then do read it, if you wish.

But even more precious to me are some words from the Bible that I have found to be true. These words say that God is ‘the Lifter of my head’.

And I often think he uses Hazel to lift it.

A further note to the reader:

After carefully crafting these sombre reflections, I discover from speaking with the owners of the lake in question that (to my initial dismay) ‘Heron’ is in fact, known locally, as ‘Brian.’

Thanks for the laughs, Brian.

Life is hilarious too.

I hope you managed to grab some lunch.


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Fixed

Photo by Trym Nilsen on Unsplash

Today I cleaned the blinds, slat by slat.
Wiping away layers of dust, marked with fingerprints that have gathered stealthily.
Unnoticed.
Hidden until they were not.

I noticed them first thing.
Shafts of early morning sunlight exposing each tiny particle.
Each mark, each imprint.
Light has a tendency to do that; expose things.

I noticed one of the blinds was broken.
Not functioning as it should, no matter how much I tugged or pushed or pulled.
How long has this blind been like this?
I’m not sure if anyone else has noticed, perhaps just me.

Anyway, I think I’ve got away with it.
A broken blind can wait, there are other jobs ahead in the queue.
It’s not something I am able to fix, I don’t have the resources, time or skill.
But at least cleaning it today helps take my mind off the fact that I have been unable to fix you.

You and I are good at waiting; long overdue appointments they said you badly need.
Another day, another week or month, even year; I lose track as the dust continues to settle.
For the present, I’ll find something else in our lives to polish, clean or mend.
As it remains one of the greatest of honours in my life to do everything I can for you.

I began by naming this poem “Broken” but then I remembered: I’ve pitched my tent in the land of hope.

So instead I’ve called it

Fixed.

#Downsyndrome #Acts2:26 #Caring #Carersweek #parentcarer


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Pass the tissues

Photo by Daniël Maas on Unsplash

Am I allowed to think about a world without you in it?

Dare I imagine what that would be like? 

I think I’m supposed to say that I can’t, I shouldn’t

But I can, I do, I lived it once; my life, without you. 

A life where your laughter would not erupt out of nowhere.

Chasing me around corners to share a joke I do not understand. 

Catching me off guard in a moment of melancholy. 

A life of contagion, where your joy could not be quarantined.

Come to think of it, you’ve never once tried to stifle a sneeze. 

I think I would hate it if you do.

So pass the tissues please,

I know I’d be sad with a life without you. 

“Our joy is not confined to ourselves but radiates out to all.” Center for Action & Contemplation

#Downsyndrome

#DownrightJoy


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Tagged

Photo by Marek Studzinski on Unsplash

I love her.

With every ounce of my being for every fibre of hers, I love her.

When I speak her beautiful name, Hazel; I love her.

When I think of her radiant face, her almond shaped eyes, I love her.

A violation of social norms; my love for her – my love.

How did I once believe I could not express or even feel this kind of love for her?

Who convinced me to ever doubt its existence?

Robbing me of those early precious moments.

Stolen time squandered on falsehood and fear; on Down’s syndrome, but not on her.

We were uninsured against such a heinous crime.

I love her precious, peculiar ways.

Pursuing unmarked pathways, she searches out joy.

Holding in her hands, the only navigation system she knows or needs: this moment.

Along these mystic trails I follow her, entering worlds of rituals and discovery.

A journey begun in hospital corridors that signposted a different way, on clinic walls painted with despair.

Uncertainty has become constant in our lives.

Walking hand in hand with each other and with faith, it is the only certain thing we possess.

Apart from my love for her, my love.

Under cover of prevailing gloom, we graffitied those hospital corridors as we left.

Tagged them with love as markers of hope, we committed our heinous crime.

#WDSD23 #DownSyndrome #Love #Hope #Humanity