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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Procession

Photo by Rob Tarren Photography

I walked alongside you, guiding you down the aisle.

Ribbon Girl.

An honour I never dreamt I’d be given. Through a sea of Faces who, quite rightly, were looking at you, not me. An unconventional Bridesmaid, no floaty dress or flowers to hold. You would have thrown those away in seconds. Your entrance had an air of tumultuous serenity as you stomped your way to the front, heavy footed, row by row.

You did not know why you were there, but knowing why has never really mattered to you. You are so often content to just be in the moment; especially when those moments are surrounded by this much care, this much thought, this much love. You even paused in your ceremonial duties; stopping to observe an unfamiliar but friendly, smiley, beaming Face.

It’s a Tea Pot kind of face, not a Coffee Pot Face.

There are no long, drawn out frowns here today. This strangest of journeys is filled with Tea Pot Faces that beam achingly wide, from handle to spout. Tears, of course….but none sorrowful.

I tug at your sleeve, prompting you to take a few more steps. Bridesmaids are supposed to keep moving, not hold up the procession. You have not reached the end of the aisle yet, and there are more Faces to look into as you expertly wave your ribbons of ivory and green. Ribbon waving is a serious occupation, and you are well practised in this art.

You glance with some puzzlement into the Faces of those who know you well and the Faces of those who don’t. Faces of those who have heard all about you many times from those who love you dearly; notably on this occasion, the Bride and her Groom. They have honoured you amongst their friends without realising; in every conversation, every photo shared, every story of you that they have so fondly and often told. There is no advocacy superior to this.

These are Faces that do not display any expressions of prejudice they may once have worn, before they heard about you.

These are Tea Pot Faces, not Coffee Pot Faces.

Smiling at you, beaming at you. They do not frown at you with long, pitying glances or worse, stares. We’ve been in those processions too. Neither do they watch you from behind a camera lens, capturing this precious moment and missing it at the same time. They have been asked to enjoy the occasion without such distractions. You, of course, do not need to be asked.

These are Faces turned in readiness to welcome you.

It hasn’t always been this way. Scrutiny has followed you since before you were born, its motives not always for your best. I am glad when the cameras are put away, for only then can you truly be seen for who you really are.

You reached the end of the aisle. Your wheelchair waiting to give rest to your braced ankles and feet. Relieved of your duties, still you clutched your ribbons. You would need these later, at the Wedding Disco, where you would show the Faces how to wave them too, with much joy. You always have plentiful supply to go round for those willing to receive; ribbons and joy.

The Bride made her entrance and rightfully took upon herself the loving, welcoming gaze of all the beaming Faces. You had gone ahead and performed your responsibilities; preparing the crowd for her Magnificent Arrival.

I like to imagine you were simply returning the favour.

The tone, the welcome, the love, had long been established by those who truly know you, your sisters, their husbands, your entire family, your friends, their friends. You are so very loved. In life, in your life, my longing is that you will always be surrounded by these kinds of Faces. A Procession of Faces that stop you in your tracks and make you want to study them, spend time with them, showing them your ribbons and teaching them how to dance with you.

A Procession interspersed with the Faces who perhaps, like me, once used to only drink from a Pot of Coffee, and now much prefer a Pot of Tea.

#Downsyndrome


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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


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Monday’s Child

Photo by Daniel Watson on Unsplash

Monday’s child went to school,

As she does, as a rule.

She was quieter than of late

The teacher said.

I’ll keep an eye, said I

Tuesday’s child stayed at home, unwell.

As she often is: not well.

We passed the time

Singing songs in rhyme.

Tube feeding, tea drinking, clock watching our day away.

Wednesday’s child remained off school.

It’s never just one day, as a rule.

We built a den,

And dreamed of when

She would be well, not ill again.

Thursday’s child went back to school

Was this the right call or was I a fool?

It mattered not,

The door was shut.

Turned away, for no teacher was well enough to teach her that day.

Friday’s child is in the lap of the gods!

Her parents and teachers are in no way at odds.

But days lost mount; by a quarter, I counted up.

As Educators told by those in power to pipe down, get on, shut up.

In schools, in SEND, and in our home, a week is a mountain to climb and a very long time

Saturday’s child and Sunday’s child

Remain as before, weekend care needs refuse to yield.

But hope has space to grow; assisting with next week’s worries to beat.

Like will Thursday’s child be on repeat?

I’ll keep an eye, say I.


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Bucket List

Photo by Phil Hearing on Unsplash

What’s the correct name for it? The sparkle you get on the surface of the sea especially in summer…… as sunlight catches the ripples, usually on a calm day. A gently moving carpet of glittering diamonds, shimmering and shimmying as far as the eye can see. 

I’m not sure there is a name for it. It’s far too beautiful a sight to be contained by a single word. It takes my breath away every time I see it, which is not that often as I do not live by the sea.

I wonder if I would tire of this sight if I did? It’s a sight I long to see every year. Most years I’ve been blessed enough to see it. It makes me smile. Every single time

I don’t have a Bucket List. You know the sort of thing, a list of places I want to visit in my lifetime, and or experiences I want to have at least once before I die. A cruise perhaps, or a trip to the Northern Lights. I’ve never fancied jumping out of a plane but I wouldn’t say no to a Trip on The Orient Express. Or Vienna. I’d quite like to visit Vienna. But I don’t have a Bucket List. I don’t really have a list at all.

Bucket lists are hard to fulfill when you are the main carer for someone you love. A list filled with experiences that may never happen simply because to make them happen would require the movement of both heaven and earth for most carers and the one(s) they care for. I don’t think many would deny that being an unpaid carer involves a level of sacrifice and loneliness that most people will never have to give or experience…unless they become one themselves, that is. Not only that, but the name Bucket List doesn’t sit well with me, it feels sort of depressing; though of course I know that one day I will ‘kick the bucket’ like every other mortal on the planet. 

Personally speaking, having a Bucket List is a pressure I can happily live without.  Don’t get me wrong, I would love (I think) every one of those experiences I mentioned and may have dreamt about as well as more, should they ever come my way. For now, and for the foreseeable future (which is a strange thing to say I always think, because the future is not really foreseeable for any of us) I am content to enjoy those experiences that often come with no name but that make me smile, make me catch my breath. And there are some I don’t enjoy at all that are also to be collected, valued even.

Some happen to me occasionally, like visits to the seaside. Others daily, hourly. Often.

Like the moment my daughter, who has Down’s syndrome, laughs out loud at who knows what. It’s a mystery but it’s very funny.

Or the moment she is given shoes that don’t rub her little feet red raw anymore, along with splints that fit correctly. She marches off, instead of hobbling. Her legs still tire, and when they do she beams as she sits back into her wheelchair. She cannot tell me her joy or her pain in words as she has none. These moments sparkle as much as the sea sparkles in the height of summer.

Or the moment her sister instinctively helps her off with her coat or shares an armchair with her. Though she shares more than an armchair; she shares her time, her attention, her love. Getting back in return seemingly nothing sometimes, but in reality everything and more. What is the name for that? Some say siblings of people with Down’s syndrome suffer. They give it a name, even though they have never sat in the same armchair, or taken off her coat. How dare they so falsely name an experience of which they know so little.

Sometimes it is the moment just after another procedure, operation or clinic appointment. Heart heavy with loving her through yet more trauma. Hers and mine. Tear stained walks along hospital corridors, telling myself and her “It’s over now, it’s ok, we’re going home”. Knowing that it’s only over until the next time. Knowing that it doesn’t really get easier. 

Even the kindness of the medics can be painful and I have been known to crumple.

These moments are harsh, but they are also profoundly beautiful. The love swells, mingled with pain, making it ever more precious.

Oh but I do have a Bucket and I am very fond of it. It’s not shiny, it has holes and probably needs a good clean. Yet it is filled with experiences I would never have imagined possible before I was gifted the responsibility and privilege of caring for this disabled child and her sister. 

Many of these experiences have no name, some are incredibly painful, others joyful beyond measure; and I treasure them all.


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Sacred

My non verbal daughter has no words, only sounds.

Sacred sounds, echoing throughout the kitchen temple; our church.

Where sacrifice and worship and silent gasping prayers rise, mingled with coffee and toast and sudocrem.

There are crumbs in the butter again.

Mmmmm is one of those sounds,

And that is the sound of my name.

Immanuel. This is God with us; with me.

Here.